Yum, tasty mutations...

MutationTaster - study a chromosomal position

 MTQE documentation
NEVER press reload or F5 - unless you want to start from the very beginning.
input seems to be ok - now mapping the variant to the different transcripts...
found 7 transcript(s)...
Querying Taster for transcript #1: ENST00000356098
Querying Taster for transcript #2: ENST00000216124
Querying Taster for transcript #3: ENST00000395621
Querying Taster for transcript #4: ENST00000453344
Querying Taster for transcript #5: ENST00000395619
Querying Taster for transcript #6: ENST00000547307
Querying Taster for transcript #7: ENST00000547805
MT speed 0 s - this script 7.559957 s

Results

genesymbolpredictionprobabilitymodelprediction
problem		splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
ARSApolymorphism_automatic0.955104301461438simple_aaeaffectedN352Ssingle base exchangers2071421show file
ARSApolymorphism_automatic0.955104301461438simple_aaeaffectedN352Ssingle base exchangers2071421show file
ARSApolymorphism_automatic0.955104301461438simple_aaeaffectedN352Ssingle base exchangers2071421show file
ARSApolymorphism_automatic0.955104301461438simple_aaeaffectedN352Ssingle base exchangers2071421show file
ARSApolymorphism_automatic0.966068079310385simple_aaeaffectedN350Ssingle base exchangers2071421show file
ARSApolymorphism_automatic0.966068079310385simple_aaeaffectedN350Ssingle base exchangers2071421show file
ARSApolymorphism_automatic0.992346168517925simple_aaeaffectedN266Ssingle base exchangers2071421show file

Taster files

Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 0.0448956985385625 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • known disease mutation at this position (HGMD CM890013)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr22:51064416T>CN/A show variant in all transcripts   IGV
HGNC symbol ARSA
Ensembl transcript ID ENST00000356098
Genbank transcript ID NM_001085426
UniProt peptide P15289
alteration type single base exchange
alteration region CDS
DNA changes c.1055A>G
cDNA.1293A>G
g.2192A>G
AA changes N352S Score: 46 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 352
frameshift no
known variant Reference ID: rs2071421
databasehomozygous (C/C)heterozygousallele carriers
1000G167792959
ExAC83970017840

known disease mutation at this position, please check HGMD for details (HGMD ID CM890013)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H2BK5me1, Histone, Histone 2B Lysine 5 mono-methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.8460.107
1.9670.961
(flanking)1.8580.997
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased2203wt: 0.4200 / mu: 0.4229 (marginal change - not scored)wt: CACTGCCCAATGTCACCTTGGATGGCTTTGACCTCAGCCCC
mu: CACTGCCCAGTGTCACCTTGGATGGCTTTGACCTCAGCCCC		 ttgg|ATGG
Acc marginally increased2190wt: 0.2262 / mu: 0.2490 (marginal change - not scored)wt: CTGGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTT
mu: CTGGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTT		 gccc|AATG
Donor gained21860.85mu: CCCACTGCCCAGTGT CACT|gccc
distance from splice site 53
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      352TLAALAGAPLPNVTLDGFDLSPLL
mutated  all conserved    352TLAALAGAPLPSVTLDGFDL
Ptroglodytes  all identical  ENSPTRG00000014550  351TLAALAGAPLPNVTLDGFDLSPL
Mmulatta  all identical  ENSMMUG00000016274  350TLAALAGAPLPNVTLDGFDLSP
Fcatus  all identical  ENSFCAG00000010597  352TLAALTGAPLPNVTLDGVDL
Mmusculus  all identical  ENSMUSG00000022620  349TLAALTGAPLPNVTLDGVDISPL
Ggallus  all identical  ENSGALG00000009746  342TLTALAGAALPNVSLDGYDLSPL
Trubripes  not conserved  ENSTRUG00000012206  352TIASLAGAKLPQVMLDGVDMSNI
Drerio  not conserved  ENSDARG00000042270  353TFAKLAGAPLPEVQLDGVEMTDI
Dmelanogaster  no homologue    
Celegans  no alignment  D1014.1  n/a
Xtropicalis  all identical  ENSXETG00000033466  352TIAALTGAPLPNVTLDGYDLSKL
protein features
start (aa)end (aa)featuredetails 
350350CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
359363HELIXmight get lost (downstream of altered splice site)
372375STRANDmight get lost (downstream of altered splice site)
382384TURNmight get lost (downstream of altered splice site)
387391STRANDmight get lost (downstream of altered splice site)
394400STRANDmight get lost (downstream of altered splice site)
404406HELIXmight get lost (downstream of altered splice site)
408410STRANDmight get lost (downstream of altered splice site)
412414HELIXmight get lost (downstream of altered splice site)
414414DISULFIDmight get lost (downstream of altered splice site)
421430STRANDmight get lost (downstream of altered splice site)
431433TURNmight get lost (downstream of altered splice site)
450469HELIXmight get lost (downstream of altered splice site)
477479HELIXmight get lost (downstream of altered splice site)
483485HELIXmight get lost (downstream of altered splice site)
488488DISULFIDmight get lost (downstream of altered splice site)
489489DISULFIDmight get lost (downstream of altered splice site)
493493DISULFIDmight get lost (downstream of altered splice site)
496499TURNmight get lost (downstream of altered splice site)
499499DISULFIDmight get lost (downstream of altered splice site)
500500DISULFIDmight get lost (downstream of altered splice site)
502502DISULFIDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1530 / 1530
position (AA) of stopcodon in wt / mu AA sequence 510 / 510
position of stopcodon in wt / mu cDNA 1768 / 1768
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 239 / 239
chromosome 22
strand -1
last intron/exon boundary 1449
theoretical NMD boundary in CDS 1160
length of CDS 1530
coding sequence (CDS) position 1055
cDNA position
(for ins/del: last normal base / first normal base)		 1293
gDNA position
(for ins/del: last normal base / first normal base)		 2192
chromosomal position
(for ins/del: last normal base / first normal base)		 51064416
original gDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered gDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
original cDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered cDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
wildtype AA sequence MSMGAPRSLL LALAAGLAVA RPPNIVLIFA DDLGYGDLGC YGHPSSTTPN LDQLAAGGLR
FTDFYVPVSL CTPSRAALLT GRLPVRMGMY PGVLVPSSRG GLPLEEVTVA EVLAARGYLT
GMAGKWHLGV GPEGAFLPPH QGFHRFLGIP YSHDQGPCQN LTCFPPATPC DGGCDQGLVP
IPLLANLSVE AQPPWLPGLE ARYMAFAHDL MADAQRQDRP FFLYYASHHT HYPQFSGQSF
AERSGRGPFG DSLMELDAAV GTLMTAIGDL GLLEETLVIF TADNGPETMR MSRGGCSGLL
RCGKGTTYEG GVREPALAFW PGHIAPGVTH ELASSLDLLP TLAALAGAPL PNVTLDGFDL
SPLLLGTGKS PRQSLFFYPS YPDEVRGVFA VRTGKYKAHF FTQGSAHSDT TADPACHASS
SLTAHEPPLL YDLSKDPGEN YNLLGGVAGA TPEVLQALKQ LQLLKAQLDA AVTFGPSQVA
RGEDPALQIC CHPGCTPRPA CCHCPDPHA*
mutated AA sequence MSMGAPRSLL LALAAGLAVA RPPNIVLIFA DDLGYGDLGC YGHPSSTTPN LDQLAAGGLR
FTDFYVPVSL CTPSRAALLT GRLPVRMGMY PGVLVPSSRG GLPLEEVTVA EVLAARGYLT
GMAGKWHLGV GPEGAFLPPH QGFHRFLGIP YSHDQGPCQN LTCFPPATPC DGGCDQGLVP
IPLLANLSVE AQPPWLPGLE ARYMAFAHDL MADAQRQDRP FFLYYASHHT HYPQFSGQSF
AERSGRGPFG DSLMELDAAV GTLMTAIGDL GLLEETLVIF TADNGPETMR MSRGGCSGLL
RCGKGTTYEG GVREPALAFW PGHIAPGVTH ELASSLDLLP TLAALAGAPL PSVTLDGFDL
SPLLLGTGKS PRQSLFFYPS YPDEVRGVFA VRTGKYKAHF FTQGSAHSDT TADPACHASS
SLTAHEPPLL YDLSKDPGEN YNLLGGVAGA TPEVLQALKQ LQLLKAQLDA AVTFGPSQVA
RGEDPALQIC CHPGCTPRPA CCHCPDPHA*
speed 1.31 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 0.0448956985385625 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • known disease mutation at this position (HGMD CM890013)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr22:51064416T>CN/A show variant in all transcripts   IGV
HGNC symbol ARSA
Ensembl transcript ID ENST00000216124
Genbank transcript ID NM_000487
UniProt peptide P15289
alteration type single base exchange
alteration region CDS
DNA changes c.1055A>G
cDNA.1448A>G
g.2192A>G
AA changes N352S Score: 46 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 352
frameshift no
known variant Reference ID: rs2071421
databasehomozygous (C/C)heterozygousallele carriers
1000G167792959
ExAC83970017840

known disease mutation at this position, please check HGMD for details (HGMD ID CM890013)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H2BK5me1, Histone, Histone 2B Lysine 5 mono-methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.8460.107
1.9670.961
(flanking)1.8580.997
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased2203wt: 0.4200 / mu: 0.4229 (marginal change - not scored)wt: CACTGCCCAATGTCACCTTGGATGGCTTTGACCTCAGCCCC
mu: CACTGCCCAGTGTCACCTTGGATGGCTTTGACCTCAGCCCC		 ttgg|ATGG
Acc marginally increased2190wt: 0.2262 / mu: 0.2490 (marginal change - not scored)wt: CTGGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTT
mu: CTGGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTT		 gccc|AATG
Donor gained21860.85mu: CCCACTGCCCAGTGT CACT|gccc
distance from splice site 53
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      352TLAALAGAPLPNVTLDGFDLSPLL
mutated  all conserved    352TLAALAGAPLPSVTLDGFDL
Ptroglodytes  all identical  ENSPTRG00000014550  351TLAALAGAPLPNVTLDGFDLSPL
Mmulatta  all identical  ENSMMUG00000016274  350TLAALAGAPLPNVTLDGFDLSP
Fcatus  all identical  ENSFCAG00000010597  352TLAALTGAPLPNVTLDGVDL
Mmusculus  all identical  ENSMUSG00000022620  349TLAALTGAPLPNVTLDGVDISPL
Ggallus  all identical  ENSGALG00000009746  342TLTALAGAALPNVSLDGYDLSPL
Trubripes  not conserved  ENSTRUG00000012206  352TIASLAGAKLPQVMLDGVDMSNI
Drerio  not conserved  ENSDARG00000042270  353TFAKLAGAPLPEVQLDGVEMTDI
Dmelanogaster  no homologue    
Celegans  no alignment  D1014.1  n/a
Xtropicalis  all identical  ENSXETG00000033466  352TIAALTGAPLPNVTLDGYDLSKL
protein features
start (aa)end (aa)featuredetails 
350350CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
359363HELIXmight get lost (downstream of altered splice site)
372375STRANDmight get lost (downstream of altered splice site)
382384TURNmight get lost (downstream of altered splice site)
387391STRANDmight get lost (downstream of altered splice site)
394400STRANDmight get lost (downstream of altered splice site)
404406HELIXmight get lost (downstream of altered splice site)
408410STRANDmight get lost (downstream of altered splice site)
412414HELIXmight get lost (downstream of altered splice site)
414414DISULFIDmight get lost (downstream of altered splice site)
421430STRANDmight get lost (downstream of altered splice site)
431433TURNmight get lost (downstream of altered splice site)
450469HELIXmight get lost (downstream of altered splice site)
477479HELIXmight get lost (downstream of altered splice site)
483485HELIXmight get lost (downstream of altered splice site)
488488DISULFIDmight get lost (downstream of altered splice site)
489489DISULFIDmight get lost (downstream of altered splice site)
493493DISULFIDmight get lost (downstream of altered splice site)
496499TURNmight get lost (downstream of altered splice site)
499499DISULFIDmight get lost (downstream of altered splice site)
500500DISULFIDmight get lost (downstream of altered splice site)
502502DISULFIDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1530 / 1530
position (AA) of stopcodon in wt / mu AA sequence 510 / 510
position of stopcodon in wt / mu cDNA 1923 / 1923
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 394 / 394
chromosome 22
strand -1
last intron/exon boundary 1604
theoretical NMD boundary in CDS 1160
length of CDS 1530
coding sequence (CDS) position 1055
cDNA position
(for ins/del: last normal base / first normal base)		 1448
gDNA position
(for ins/del: last normal base / first normal base)		 2192
chromosomal position
(for ins/del: last normal base / first normal base)		 51064416
original gDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered gDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
original cDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered cDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
wildtype AA sequence MSMGAPRSLL LALAAGLAVA RPPNIVLIFA DDLGYGDLGC YGHPSSTTPN LDQLAAGGLR
FTDFYVPVSL CTPSRAALLT GRLPVRMGMY PGVLVPSSRG GLPLEEVTVA EVLAARGYLT
GMAGKWHLGV GPEGAFLPPH QGFHRFLGIP YSHDQGPCQN LTCFPPATPC DGGCDQGLVP
IPLLANLSVE AQPPWLPGLE ARYMAFAHDL MADAQRQDRP FFLYYASHHT HYPQFSGQSF
AERSGRGPFG DSLMELDAAV GTLMTAIGDL GLLEETLVIF TADNGPETMR MSRGGCSGLL
RCGKGTTYEG GVREPALAFW PGHIAPGVTH ELASSLDLLP TLAALAGAPL PNVTLDGFDL
SPLLLGTGKS PRQSLFFYPS YPDEVRGVFA VRTGKYKAHF FTQGSAHSDT TADPACHASS
SLTAHEPPLL YDLSKDPGEN YNLLGGVAGA TPEVLQALKQ LQLLKAQLDA AVTFGPSQVA
RGEDPALQIC CHPGCTPRPA CCHCPDPHA*
mutated AA sequence MSMGAPRSLL LALAAGLAVA RPPNIVLIFA DDLGYGDLGC YGHPSSTTPN LDQLAAGGLR
FTDFYVPVSL CTPSRAALLT GRLPVRMGMY PGVLVPSSRG GLPLEEVTVA EVLAARGYLT
GMAGKWHLGV GPEGAFLPPH QGFHRFLGIP YSHDQGPCQN LTCFPPATPC DGGCDQGLVP
IPLLANLSVE AQPPWLPGLE ARYMAFAHDL MADAQRQDRP FFLYYASHHT HYPQFSGQSF
AERSGRGPFG DSLMELDAAV GTLMTAIGDL GLLEETLVIF TADNGPETMR MSRGGCSGLL
RCGKGTTYEG GVREPALAFW PGHIAPGVTH ELASSLDLLP TLAALAGAPL PSVTLDGFDL
SPLLLGTGKS PRQSLFFYPS YPDEVRGVFA VRTGKYKAHF FTQGSAHSDT TADPACHASS
SLTAHEPPLL YDLSKDPGEN YNLLGGVAGA TPEVLQALKQ LQLLKAQLDA AVTFGPSQVA
RGEDPALQIC CHPGCTPRPA CCHCPDPHA*
speed 1.46 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 0.0448956985385625 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • known disease mutation at this position (HGMD CM890013)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr22:51064416T>CN/A show variant in all transcripts   IGV
HGNC symbol ARSA
Ensembl transcript ID ENST00000395621
Genbank transcript ID N/A
UniProt peptide P15289
alteration type single base exchange
alteration region CDS
DNA changes c.1055A>G
cDNA.1326A>G
g.2192A>G
AA changes N352S Score: 46 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 352
frameshift no
known variant Reference ID: rs2071421
databasehomozygous (C/C)heterozygousallele carriers
1000G167792959
ExAC83970017840

known disease mutation at this position, please check HGMD for details (HGMD ID CM890013)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H2BK5me1, Histone, Histone 2B Lysine 5 mono-methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.8460.107
1.9670.961
(flanking)1.8580.997
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased2203wt: 0.4200 / mu: 0.4229 (marginal change - not scored)wt: CACTGCCCAATGTCACCTTGGATGGCTTTGACCTCAGCCCC
mu: CACTGCCCAGTGTCACCTTGGATGGCTTTGACCTCAGCCCC		 ttgg|ATGG
Acc marginally increased2190wt: 0.2262 / mu: 0.2490 (marginal change - not scored)wt: CTGGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTT
mu: CTGGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTT		 gccc|AATG
Donor gained21860.85mu: CCCACTGCCCAGTGT CACT|gccc
distance from splice site 53
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      352TLAALAGAPLPNVTLDGFDLSPLL
mutated  all conserved    352TLAALAGAPLPSVTLDGFDL
Ptroglodytes  all identical  ENSPTRG00000014550  351TLAALAGAPLPNVTLDGFDLSPL
Mmulatta  all identical  ENSMMUG00000016274  350TLAALAGAPLPNVTLDGFDLSP
Fcatus  all identical  ENSFCAG00000010597  352TLAALTGAPLPNVTLDGVDL
Mmusculus  all identical  ENSMUSG00000022620  349TLAALTGAPLPNVTLDGVDISPL
Ggallus  all identical  ENSGALG00000009746  342TLTALAGAALPNVSLDGYDLSPL
Trubripes  not conserved  ENSTRUG00000012206  352TIASLAGAKLPQVMLDGVDMSNI
Drerio  not conserved  ENSDARG00000042270  353TFAKLAGAPLPEVQLDGVEMTDI
Dmelanogaster  no homologue    
Celegans  no alignment  D1014.1  n/a
Xtropicalis  all identical  ENSXETG00000033466  352TIAALTGAPLPNVTLDGYDLSKL
protein features
start (aa)end (aa)featuredetails 
350350CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
359363HELIXmight get lost (downstream of altered splice site)
372375STRANDmight get lost (downstream of altered splice site)
382384TURNmight get lost (downstream of altered splice site)
387391STRANDmight get lost (downstream of altered splice site)
394400STRANDmight get lost (downstream of altered splice site)
404406HELIXmight get lost (downstream of altered splice site)
408410STRANDmight get lost (downstream of altered splice site)
412414HELIXmight get lost (downstream of altered splice site)
414414DISULFIDmight get lost (downstream of altered splice site)
421430STRANDmight get lost (downstream of altered splice site)
431433TURNmight get lost (downstream of altered splice site)
450469HELIXmight get lost (downstream of altered splice site)
477479HELIXmight get lost (downstream of altered splice site)
483485HELIXmight get lost (downstream of altered splice site)
488488DISULFIDmight get lost (downstream of altered splice site)
489489DISULFIDmight get lost (downstream of altered splice site)
493493DISULFIDmight get lost (downstream of altered splice site)
496499TURNmight get lost (downstream of altered splice site)
499499DISULFIDmight get lost (downstream of altered splice site)
500500DISULFIDmight get lost (downstream of altered splice site)
502502DISULFIDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1530 / 1530
position (AA) of stopcodon in wt / mu AA sequence 510 / 510
position of stopcodon in wt / mu cDNA 1801 / 1801
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 272 / 272
chromosome 22
strand -1
last intron/exon boundary 1482
theoretical NMD boundary in CDS 1160
length of CDS 1530
coding sequence (CDS) position 1055
cDNA position
(for ins/del: last normal base / first normal base)		 1326
gDNA position
(for ins/del: last normal base / first normal base)		 2192
chromosomal position
(for ins/del: last normal base / first normal base)		 51064416
original gDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered gDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
original cDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered cDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
wildtype AA sequence MSMGAPRSLL LALAAGLAVA RPPNIVLIFA DDLGYGDLGC YGHPSSTTPN LDQLAAGGLR
FTDFYVPVSL CTPSRAALLT GRLPVRMGMY PGVLVPSSRG GLPLEEVTVA EVLAARGYLT
GMAGKWHLGV GPEGAFLPPH QGFHRFLGIP YSHDQGPCQN LTCFPPATPC DGGCDQGLVP
IPLLANLSVE AQPPWLPGLE ARYMAFAHDL MADAQRQDRP FFLYYASHHT HYPQFSGQSF
AERSGRGPFG DSLMELDAAV GTLMTAIGDL GLLEETLVIF TADNGPETMR MSRGGCSGLL
RCGKGTTYEG GVREPALAFW PGHIAPGVTH ELASSLDLLP TLAALAGAPL PNVTLDGFDL
SPLLLGTGKS PRQSLFFYPS YPDEVRGVFA VRTGKYKAHF FTQGSAHSDT TADPACHASS
SLTAHEPPLL YDLSKDPGEN YNLLGGVAGA TPEVLQALKQ LQLLKAQLDA AVTFGPSQVA
RGEDPALQIC CHPGCTPRPA CCHCPDPHA*
mutated AA sequence MSMGAPRSLL LALAAGLAVA RPPNIVLIFA DDLGYGDLGC YGHPSSTTPN LDQLAAGGLR
FTDFYVPVSL CTPSRAALLT GRLPVRMGMY PGVLVPSSRG GLPLEEVTVA EVLAARGYLT
GMAGKWHLGV GPEGAFLPPH QGFHRFLGIP YSHDQGPCQN LTCFPPATPC DGGCDQGLVP
IPLLANLSVE AQPPWLPGLE ARYMAFAHDL MADAQRQDRP FFLYYASHHT HYPQFSGQSF
AERSGRGPFG DSLMELDAAV GTLMTAIGDL GLLEETLVIF TADNGPETMR MSRGGCSGLL
RCGKGTTYEG GVREPALAFW PGHIAPGVTH ELASSLDLLP TLAALAGAPL PSVTLDGFDL
SPLLLGTGKS PRQSLFFYPS YPDEVRGVFA VRTGKYKAHF FTQGSAHSDT TADPACHASS
SLTAHEPPLL YDLSKDPGEN YNLLGGVAGA TPEVLQALKQ LQLLKAQLDA AVTFGPSQVA
RGEDPALQIC CHPGCTPRPA CCHCPDPHA*
speed 1.40 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 0.0448956985385625 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • known disease mutation at this position (HGMD CM890013)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr22:51064416T>CN/A show variant in all transcripts   IGV
HGNC symbol ARSA
Ensembl transcript ID ENST00000395619
Genbank transcript ID NM_001085427
UniProt peptide P15289
alteration type single base exchange
alteration region CDS
DNA changes c.1055A>G
cDNA.1237A>G
g.2192A>G
AA changes N352S Score: 46 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 352
frameshift no
known variant Reference ID: rs2071421
databasehomozygous (C/C)heterozygousallele carriers
1000G167792959
ExAC83970017840

known disease mutation at this position, please check HGMD for details (HGMD ID CM890013)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H2BK5me1, Histone, Histone 2B Lysine 5 mono-methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.8460.107
1.9670.961
(flanking)1.8580.997
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased2203wt: 0.4200 / mu: 0.4229 (marginal change - not scored)wt: CACTGCCCAATGTCACCTTGGATGGCTTTGACCTCAGCCCC
mu: CACTGCCCAGTGTCACCTTGGATGGCTTTGACCTCAGCCCC		 ttgg|ATGG
Acc marginally increased2190wt: 0.2262 / mu: 0.2490 (marginal change - not scored)wt: CTGGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTT
mu: CTGGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTT		 gccc|AATG
Donor gained21860.85mu: CCCACTGCCCAGTGT CACT|gccc
distance from splice site 53
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      352TLAALAGAPLPNVTLDGFDLSPLL
mutated  all conserved    352TLAALAGAPLPSVTLDGFDL
Ptroglodytes  all identical  ENSPTRG00000014550  351TLAALAGAPLPNVTLDGFDLSPL
Mmulatta  all identical  ENSMMUG00000016274  350TLAALAGAPLPNVTLDGFDLSP
Fcatus  all identical  ENSFCAG00000010597  352TLAALTGAPLPNVTLDGVDL
Mmusculus  all identical  ENSMUSG00000022620  349TLAALTGAPLPNVTLDGVDISPL
Ggallus  all identical  ENSGALG00000009746  342TLTALAGAALPNVSLDGYDLSPL
Trubripes  not conserved  ENSTRUG00000012206  352TIASLAGAKLPQVMLDGVDMSNI
Drerio  not conserved  ENSDARG00000042270  353TFAKLAGAPLPEVQLDGVEMTDI
Dmelanogaster  no homologue    
Celegans  no alignment  D1014.1  n/a
Xtropicalis  all identical  ENSXETG00000033466  352TIAALTGAPLPNVTLDGYDLSKL
protein features
start (aa)end (aa)featuredetails 
350350CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
359363HELIXmight get lost (downstream of altered splice site)
372375STRANDmight get lost (downstream of altered splice site)
382384TURNmight get lost (downstream of altered splice site)
387391STRANDmight get lost (downstream of altered splice site)
394400STRANDmight get lost (downstream of altered splice site)
404406HELIXmight get lost (downstream of altered splice site)
408410STRANDmight get lost (downstream of altered splice site)
412414HELIXmight get lost (downstream of altered splice site)
414414DISULFIDmight get lost (downstream of altered splice site)
421430STRANDmight get lost (downstream of altered splice site)
431433TURNmight get lost (downstream of altered splice site)
450469HELIXmight get lost (downstream of altered splice site)
477479HELIXmight get lost (downstream of altered splice site)
483485HELIXmight get lost (downstream of altered splice site)
488488DISULFIDmight get lost (downstream of altered splice site)
489489DISULFIDmight get lost (downstream of altered splice site)
493493DISULFIDmight get lost (downstream of altered splice site)
496499TURNmight get lost (downstream of altered splice site)
499499DISULFIDmight get lost (downstream of altered splice site)
500500DISULFIDmight get lost (downstream of altered splice site)
502502DISULFIDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1530 / 1530
position (AA) of stopcodon in wt / mu AA sequence 510 / 510
position of stopcodon in wt / mu cDNA 1712 / 1712
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 183 / 183
chromosome 22
strand -1
last intron/exon boundary 1393
theoretical NMD boundary in CDS 1160
length of CDS 1530
coding sequence (CDS) position 1055
cDNA position
(for ins/del: last normal base / first normal base)		 1237
gDNA position
(for ins/del: last normal base / first normal base)		 2192
chromosomal position
(for ins/del: last normal base / first normal base)		 51064416
original gDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered gDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
original cDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered cDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
wildtype AA sequence MSMGAPRSLL LALAAGLAVA RPPNIVLIFA DDLGYGDLGC YGHPSSTTPN LDQLAAGGLR
FTDFYVPVSL CTPSRAALLT GRLPVRMGMY PGVLVPSSRG GLPLEEVTVA EVLAARGYLT
GMAGKWHLGV GPEGAFLPPH QGFHRFLGIP YSHDQGPCQN LTCFPPATPC DGGCDQGLVP
IPLLANLSVE AQPPWLPGLE ARYMAFAHDL MADAQRQDRP FFLYYASHHT HYPQFSGQSF
AERSGRGPFG DSLMELDAAV GTLMTAIGDL GLLEETLVIF TADNGPETMR MSRGGCSGLL
RCGKGTTYEG GVREPALAFW PGHIAPGVTH ELASSLDLLP TLAALAGAPL PNVTLDGFDL
SPLLLGTGKS PRQSLFFYPS YPDEVRGVFA VRTGKYKAHF FTQGSAHSDT TADPACHASS
SLTAHEPPLL YDLSKDPGEN YNLLGGVAGA TPEVLQALKQ LQLLKAQLDA AVTFGPSQVA
RGEDPALQIC CHPGCTPRPA CCHCPDPHA*
mutated AA sequence MSMGAPRSLL LALAAGLAVA RPPNIVLIFA DDLGYGDLGC YGHPSSTTPN LDQLAAGGLR
FTDFYVPVSL CTPSRAALLT GRLPVRMGMY PGVLVPSSRG GLPLEEVTVA EVLAARGYLT
GMAGKWHLGV GPEGAFLPPH QGFHRFLGIP YSHDQGPCQN LTCFPPATPC DGGCDQGLVP
IPLLANLSVE AQPPWLPGLE ARYMAFAHDL MADAQRQDRP FFLYYASHHT HYPQFSGQSF
AERSGRGPFG DSLMELDAAV GTLMTAIGDL GLLEETLVIF TADNGPETMR MSRGGCSGLL
RCGKGTTYEG GVREPALAFW PGHIAPGVTH ELASSLDLLP TLAALAGAPL PSVTLDGFDL
SPLLLGTGKS PRQSLFFYPS YPDEVRGVFA VRTGKYKAHF FTQGSAHSDT TADPACHASS
SLTAHEPPLL YDLSKDPGEN YNLLGGVAGA TPEVLQALKQ LQLLKAQLDA AVTFGPSQVA
RGEDPALQIC CHPGCTPRPA CCHCPDPHA*
speed 1.31 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 0.0339319206896152 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • known disease mutation at this position (HGMD CM890013)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr22:51064416T>CN/A show variant in all transcripts   IGV
HGNC symbol ARSA
Ensembl transcript ID ENST00000547307
Genbank transcript ID N/A
UniProt peptide P15289
alteration type single base exchange
alteration region CDS
DNA changes c.1049A>G
cDNA.1455A>G
g.2192A>G
AA changes N350S Score: 46 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 350
frameshift no
known variant Reference ID: rs2071421
databasehomozygous (C/C)heterozygousallele carriers
1000G167792959
ExAC83970017840

known disease mutation at this position, please check HGMD for details (HGMD ID CM890013)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H2BK5me1, Histone, Histone 2B Lysine 5 mono-methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.8460.107
1.9670.961
(flanking)1.8580.997
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased2203wt: 0.4200 / mu: 0.4229 (marginal change - not scored)wt: CACTGCCCAATGTCACCTTGGATGGCTTTGACCTCAGCCCC
mu: CACTGCCCAGTGTCACCTTGGATGGCTTTGACCTCAGCCCC		 ttgg|ATGG
Acc marginally increased2190wt: 0.2262 / mu: 0.2490 (marginal change - not scored)wt: CTGGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTT
mu: CTGGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTT		 gccc|AATG
Donor gained21860.85mu: CCCACTGCCCAGTGT CACT|gccc
distance from splice site 53
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      350TLAALAGAPLPNVTLDGFDLSPLL
mutated  all conserved    350TLAALAGAPLPSVTLDGFDLSP
Ptroglodytes  all identical  ENSPTRG00000014550  351TLAALAGAPLPNVTLDGFDLSPL
Mmulatta  all identical  ENSMMUG00000016274  350TLAALAGAPLPNVTLDGFDLSP
Fcatus  all identical  ENSFCAG00000010597  352TLAALTGAPLPNVTLDGVDLSPL
Mmusculus  all identical  ENSMUSG00000022620  349TLAALTGAPLPNVTLDGVDISPL
Ggallus  all identical  ENSGALG00000009746  342TLTALAGAALPNVSLDGYDLSPL
Trubripes  not conserved  ENSTRUG00000012206  352TIASLAGAKLPQVMLDGVDMSNI
Drerio  not conserved  ENSDARG00000042270  353TFAKLAGAPLPEVQLDGVEMTDI
Dmelanogaster  no homologue    
Celegans  no alignment  D1014.1  n/a
Xtropicalis  all identical  ENSXETG00000033466  352TIAALTGAPLPNVTLDGYDLSKL
protein features
start (aa)end (aa)featuredetails 
350350CARBOHYDN-linked (GlcNAc...).lost
359363HELIXmight get lost (downstream of altered splice site)
372375STRANDmight get lost (downstream of altered splice site)
382384TURNmight get lost (downstream of altered splice site)
387391STRANDmight get lost (downstream of altered splice site)
394400STRANDmight get lost (downstream of altered splice site)
404406HELIXmight get lost (downstream of altered splice site)
408410STRANDmight get lost (downstream of altered splice site)
412414HELIXmight get lost (downstream of altered splice site)
414414DISULFIDmight get lost (downstream of altered splice site)
421430STRANDmight get lost (downstream of altered splice site)
431433TURNmight get lost (downstream of altered splice site)
450469HELIXmight get lost (downstream of altered splice site)
477479HELIXmight get lost (downstream of altered splice site)
483485HELIXmight get lost (downstream of altered splice site)
488488DISULFIDmight get lost (downstream of altered splice site)
489489DISULFIDmight get lost (downstream of altered splice site)
493493DISULFIDmight get lost (downstream of altered splice site)
496499TURNmight get lost (downstream of altered splice site)
499499DISULFIDmight get lost (downstream of altered splice site)
500500DISULFIDmight get lost (downstream of altered splice site)
502502DISULFIDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1524 / 1524
position (AA) of stopcodon in wt / mu AA sequence 508 / 508
position of stopcodon in wt / mu cDNA 1930 / 1930
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 407 / 407
chromosome 22
strand -1
last intron/exon boundary 1611
theoretical NMD boundary in CDS 1154
length of CDS 1524
coding sequence (CDS) position 1049
cDNA position
(for ins/del: last normal base / first normal base)		 1455
gDNA position
(for ins/del: last normal base / first normal base)		 2192
chromosomal position
(for ins/del: last normal base / first normal base)		 51064416
original gDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered gDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
original cDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered cDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
wildtype AA sequence MGAPRSLLLA LAAGLAVARP PNIVLIFADD LGYGDLGCYG HPSSTTPNLD QLAAGGLRFT
DFYVPVSLCT PSRAALLTGR LPVRMGMYPG VLVPSSRGGL PLEEVTVAEV LAARGYLTGM
AGKWHLGVGP EGAFLPPHQG FHRFLGIPYS HDQGPCQNLT CFPPATPCDG GCDQGLVPIP
LLANLSVEAQ PPWLPGLEAR YMAFAHDLMA DAQRQDRPFF LYYASHHTHY PQFSGQSFAE
RSGRGPFGDS LMELDAAVGT LMTAIGDLGL LEETLVIFTA DNGPETMRMS RGGCSGLLRC
GKGTTYEGGV REPALAFWPG HIAPGVTHEL ASSLDLLPTL AALAGAPLPN VTLDGFDLSP
LLLGTGKSPR QSLFFYPSYP DEVRGVFAVR TGKYKAHFFT QGSAHSDTTA DPACHASSSL
TAHEPPLLYD LSKDPGENYN LLGGVAGATP EVLQALKQLQ LLKAQLDAAV TFGPSQVARG
EDPALQICCH PGCTPRPACC HCPDPHA*
mutated AA sequence MGAPRSLLLA LAAGLAVARP PNIVLIFADD LGYGDLGCYG HPSSTTPNLD QLAAGGLRFT
DFYVPVSLCT PSRAALLTGR LPVRMGMYPG VLVPSSRGGL PLEEVTVAEV LAARGYLTGM
AGKWHLGVGP EGAFLPPHQG FHRFLGIPYS HDQGPCQNLT CFPPATPCDG GCDQGLVPIP
LLANLSVEAQ PPWLPGLEAR YMAFAHDLMA DAQRQDRPFF LYYASHHTHY PQFSGQSFAE
RSGRGPFGDS LMELDAAVGT LMTAIGDLGL LEETLVIFTA DNGPETMRMS RGGCSGLLRC
GKGTTYEGGV REPALAFWPG HIAPGVTHEL ASSLDLLPTL AALAGAPLPS VTLDGFDLSP
LLLGTGKSPR QSLFFYPSYP DEVRGVFAVR TGKYKAHFFT QGSAHSDTTA DPACHASSSL
TAHEPPLLYD LSKDPGENYN LLGGVAGATP EVLQALKQLQ LLKAQLDAAV TFGPSQVARG
EDPALQICCH PGCTPRPACC HCPDPHA*
speed 1.40 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 0.0339319206896152 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • known disease mutation at this position (HGMD CM890013)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr22:51064416T>CN/A show variant in all transcripts   IGV
HGNC symbol ARSA
Ensembl transcript ID ENST00000547805
Genbank transcript ID NM_001085425
UniProt peptide P15289
alteration type single base exchange
alteration region CDS
DNA changes c.1049A>G
cDNA.1350A>G
g.2192A>G
AA changes N350S Score: 46 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 350
frameshift no
known variant Reference ID: rs2071421
databasehomozygous (C/C)heterozygousallele carriers
1000G167792959
ExAC83970017840

known disease mutation at this position, please check HGMD for details (HGMD ID CM890013)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H2BK5me1, Histone, Histone 2B Lysine 5 mono-methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.8460.107
1.9670.961
(flanking)1.8580.997
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased2203wt: 0.4200 / mu: 0.4229 (marginal change - not scored)wt: CACTGCCCAATGTCACCTTGGATGGCTTTGACCTCAGCCCC
mu: CACTGCCCAGTGTCACCTTGGATGGCTTTGACCTCAGCCCC		 ttgg|ATGG
Acc marginally increased2190wt: 0.2262 / mu: 0.2490 (marginal change - not scored)wt: CTGGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTT
mu: CTGGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTT		 gccc|AATG
Donor gained21860.85mu: CCCACTGCCCAGTGT CACT|gccc
distance from splice site 53
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      350TLAALAGAPLPNVTLDGFDLSPLL
mutated  all conserved    350TLAALAGAPLPSVTLDGFDLSP
Ptroglodytes  all identical  ENSPTRG00000014550  351TLAALAGAPLPNVTLDGFDLSPL
Mmulatta  all identical  ENSMMUG00000016274  350TLAALAGAPLPNVTLDGFDLSP
Fcatus  all identical  ENSFCAG00000010597  352TLAALTGAPLPNVTLDGVDLSPL
Mmusculus  all identical  ENSMUSG00000022620  349TLAALTGAPLPNVTLDGVDISPL
Ggallus  all identical  ENSGALG00000009746  342TLTALAGAALPNVSLDGYDLSPL
Trubripes  not conserved  ENSTRUG00000012206  352TIASLAGAKLPQVMLDGVDMSNI
Drerio  not conserved  ENSDARG00000042270  353TFAKLAGAPLPEVQLDGVEMTDI
Dmelanogaster  no homologue    
Celegans  no alignment  D1014.1  n/a
Xtropicalis  all identical  ENSXETG00000033466  352TIAALTGAPLPNVTLDGYDLSKL
protein features
start (aa)end (aa)featuredetails 
350350CARBOHYDN-linked (GlcNAc...).lost
359363HELIXmight get lost (downstream of altered splice site)
372375STRANDmight get lost (downstream of altered splice site)
382384TURNmight get lost (downstream of altered splice site)
387391STRANDmight get lost (downstream of altered splice site)
394400STRANDmight get lost (downstream of altered splice site)
404406HELIXmight get lost (downstream of altered splice site)
408410STRANDmight get lost (downstream of altered splice site)
412414HELIXmight get lost (downstream of altered splice site)
414414DISULFIDmight get lost (downstream of altered splice site)
421430STRANDmight get lost (downstream of altered splice site)
431433TURNmight get lost (downstream of altered splice site)
450469HELIXmight get lost (downstream of altered splice site)
477479HELIXmight get lost (downstream of altered splice site)
483485HELIXmight get lost (downstream of altered splice site)
488488DISULFIDmight get lost (downstream of altered splice site)
489489DISULFIDmight get lost (downstream of altered splice site)
493493DISULFIDmight get lost (downstream of altered splice site)
496499TURNmight get lost (downstream of altered splice site)
499499DISULFIDmight get lost (downstream of altered splice site)
500500DISULFIDmight get lost (downstream of altered splice site)
502502DISULFIDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1524 / 1524
position (AA) of stopcodon in wt / mu AA sequence 508 / 508
position of stopcodon in wt / mu cDNA 1825 / 1825
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 302 / 302
chromosome 22
strand -1
last intron/exon boundary 1506
theoretical NMD boundary in CDS 1154
length of CDS 1524
coding sequence (CDS) position 1049
cDNA position
(for ins/del: last normal base / first normal base)		 1350
gDNA position
(for ins/del: last normal base / first normal base)		 2192
chromosomal position
(for ins/del: last normal base / first normal base)		 51064416
original gDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered gDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
original cDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered cDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
wildtype AA sequence MGAPRSLLLA LAAGLAVARP PNIVLIFADD LGYGDLGCYG HPSSTTPNLD QLAAGGLRFT
DFYVPVSLCT PSRAALLTGR LPVRMGMYPG VLVPSSRGGL PLEEVTVAEV LAARGYLTGM
AGKWHLGVGP EGAFLPPHQG FHRFLGIPYS HDQGPCQNLT CFPPATPCDG GCDQGLVPIP
LLANLSVEAQ PPWLPGLEAR YMAFAHDLMA DAQRQDRPFF LYYASHHTHY PQFSGQSFAE
RSGRGPFGDS LMELDAAVGT LMTAIGDLGL LEETLVIFTA DNGPETMRMS RGGCSGLLRC
GKGTTYEGGV REPALAFWPG HIAPGVTHEL ASSLDLLPTL AALAGAPLPN VTLDGFDLSP
LLLGTGKSPR QSLFFYPSYP DEVRGVFAVR TGKYKAHFFT QGSAHSDTTA DPACHASSSL
TAHEPPLLYD LSKDPGENYN LLGGVAGATP EVLQALKQLQ LLKAQLDAAV TFGPSQVARG
EDPALQICCH PGCTPRPACC HCPDPHA*
mutated AA sequence MGAPRSLLLA LAAGLAVARP PNIVLIFADD LGYGDLGCYG HPSSTTPNLD QLAAGGLRFT
DFYVPVSLCT PSRAALLTGR LPVRMGMYPG VLVPSSRGGL PLEEVTVAEV LAARGYLTGM
AGKWHLGVGP EGAFLPPHQG FHRFLGIPYS HDQGPCQNLT CFPPATPCDG GCDQGLVPIP
LLANLSVEAQ PPWLPGLEAR YMAFAHDLMA DAQRQDRPFF LYYASHHTHY PQFSGQSFAE
RSGRGPFGDS LMELDAAVGT LMTAIGDLGL LEETLVIFTA DNGPETMRMS RGGCSGLLRC
GKGTTYEGGV REPALAFWPG HIAPGVTHEL ASSLDLLPTL AALAGAPLPS VTLDGFDLSP
LLLGTGKSPR QSLFFYPSYP DEVRGVFAVR TGKYKAHFFT QGSAHSDTTA DPACHASSSL
TAHEPPLLYD LSKDPGENYN LLGGVAGATP EVLQALKQLQ LLKAQLDAAV TFGPSQVARG
EDPALQICCH PGCTPRPACC HCPDPHA*
speed 1.35 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 0.00765383148207463 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • known disease mutation at this position (HGMD CM890013)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr22:51064416T>CN/A show variant in all transcripts   IGV
HGNC symbol ARSA
Ensembl transcript ID ENST00000453344
Genbank transcript ID NM_001085428
UniProt peptide P15289
alteration type single base exchange
alteration region CDS
DNA changes c.797A>G
cDNA.1059A>G
g.2192A>G
AA changes N266S Score: 46 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 266
frameshift no
known variant Reference ID: rs2071421
databasehomozygous (C/C)heterozygousallele carriers
1000G167792959
ExAC83970017840

known disease mutation at this position, please check HGMD for details (HGMD ID CM890013)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H2BK5me1, Histone, Histone 2B Lysine 5 mono-methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.8460.107
1.9670.961
(flanking)1.8580.997
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased2203wt: 0.4200 / mu: 0.4229 (marginal change - not scored)wt: CACTGCCCAATGTCACCTTGGATGGCTTTGACCTCAGCCCC
mu: CACTGCCCAGTGTCACCTTGGATGGCTTTGACCTCAGCCCC		 ttgg|ATGG
Acc marginally increased2190wt: 0.2262 / mu: 0.2490 (marginal change - not scored)wt: CTGGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTT
mu: CTGGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTT		 gccc|AATG
Donor gained21860.85mu: CCCACTGCCCAGTGT CACT|gccc
distance from splice site 53
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      266TLAALAGAPLPNVTLDGFDLSPLL
mutated  all conserved    266TLAALAGAPLPSVTLDGFDLSPL
Ptroglodytes  all identical  ENSPTRG00000014550  351TLAALAGAPLPNVTLDGFDLSPL
Mmulatta  all identical  ENSMMUG00000016274  350TLAALAGAPLPNVTLDGFDLSPL
Fcatus  all identical  ENSFCAG00000010597  352TLAALTGAPLPNVTLDGVDLSPL
Mmusculus  all identical  ENSMUSG00000022620  349TLAALTGAPLPNVTLDGVDISPL
Ggallus  all identical  ENSGALG00000009746  342TLTALAGAALPNVSLDGYDLSPL
Trubripes  not conserved  ENSTRUG00000012206  352TIASLAGAKLPQVMLDGVDMSNI
Drerio  not conserved  ENSDARG00000042270  353TFAKLAGAPLPEVQLDGVEMTDI
Dmelanogaster  no homologue    
Celegans  no alignment  D1014.1  n/a
Xtropicalis  all identical  ENSXETG00000033466  352TIAALTGAPLPNVTLDGYDLSKL
protein features
start (aa)end (aa)featuredetails 
245267HELIXlost
271273HELIXmight get lost (downstream of altered splice site)
274282STRANDmight get lost (downstream of altered splice site)
281281METALCalcium.might get lost (downstream of altered splice site)
282282METALCalcium.might get lost (downstream of altered splice site)
286291HELIXmight get lost (downstream of altered splice site)
300300DISULFIDmight get lost (downstream of altered splice site)
302302BINDINGSubstrate.might get lost (downstream of altered splice site)
304306STRANDmight get lost (downstream of altered splice site)
307310HELIXmight get lost (downstream of altered splice site)
315317STRANDmight get lost (downstream of altered splice site)
319321TURNmight get lost (downstream of altered splice site)
324327STRANDmight get lost (downstream of altered splice site)
333335HELIXmight get lost (downstream of altered splice site)
336343HELIXmight get lost (downstream of altered splice site)
350350CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
359363HELIXmight get lost (downstream of altered splice site)
372375STRANDmight get lost (downstream of altered splice site)
382384TURNmight get lost (downstream of altered splice site)
387391STRANDmight get lost (downstream of altered splice site)
394400STRANDmight get lost (downstream of altered splice site)
404406HELIXmight get lost (downstream of altered splice site)
408410STRANDmight get lost (downstream of altered splice site)
412414HELIXmight get lost (downstream of altered splice site)
414414DISULFIDmight get lost (downstream of altered splice site)
421430STRANDmight get lost (downstream of altered splice site)
431433TURNmight get lost (downstream of altered splice site)
450469HELIXmight get lost (downstream of altered splice site)
477479HELIXmight get lost (downstream of altered splice site)
483485HELIXmight get lost (downstream of altered splice site)
488488DISULFIDmight get lost (downstream of altered splice site)
489489DISULFIDmight get lost (downstream of altered splice site)
493493DISULFIDmight get lost (downstream of altered splice site)
496499TURNmight get lost (downstream of altered splice site)
499499DISULFIDmight get lost (downstream of altered splice site)
500500DISULFIDmight get lost (downstream of altered splice site)
502502DISULFIDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1272 / 1272
position (AA) of stopcodon in wt / mu AA sequence 424 / 424
position of stopcodon in wt / mu cDNA 1534 / 1534
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 263 / 263
chromosome 22
strand -1
last intron/exon boundary 1215
theoretical NMD boundary in CDS 902
length of CDS 1272
coding sequence (CDS) position 797
cDNA position
(for ins/del: last normal base / first normal base)		 1059
gDNA position
(for ins/del: last normal base / first normal base)		 2192
chromosomal position
(for ins/del: last normal base / first normal base)		 51064416
original gDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered gDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
original cDNA sequence snippet GGCTGGGGCCCCACTGCCCAATGTCACCTTGGATGGCTTTG
altered cDNA sequence snippet GGCTGGGGCCCCACTGCCCAGTGTCACCTTGGATGGCTTTG
wildtype AA sequence MGMYPGVLVP SSRGGLPLEE VTVAEVLAAR GYLTGMAGKW HLGVGPEGAF LPPHQGFHRF
LGIPYSHDQG PCQNLTCFPP ATPCDGGCDQ GLVPIPLLAN LSVEAQPPWL PGLEARYMAF
AHDLMADAQR QDRPFFLYYA SHHTHYPQFS GQSFAERSGR GPFGDSLMEL DAAVGTLMTA
IGDLGLLEET LVIFTADNGP ETMRMSRGGC SGLLRCGKGT TYEGGVREPA LAFWPGHIAP
GVTHELASSL DLLPTLAALA GAPLPNVTLD GFDLSPLLLG TGKSPRQSLF FYPSYPDEVR
GVFAVRTGKY KAHFFTQGSA HSDTTADPAC HASSSLTAHE PPLLYDLSKD PGENYNLLGG
VAGATPEVLQ ALKQLQLLKA QLDAAVTFGP SQVARGEDPA LQICCHPGCT PRPACCHCPD
PHA*
mutated AA sequence MGMYPGVLVP SSRGGLPLEE VTVAEVLAAR GYLTGMAGKW HLGVGPEGAF LPPHQGFHRF
LGIPYSHDQG PCQNLTCFPP ATPCDGGCDQ GLVPIPLLAN LSVEAQPPWL PGLEARYMAF
AHDLMADAQR QDRPFFLYYA SHHTHYPQFS GQSFAERSGR GPFGDSLMEL DAAVGTLMTA
IGDLGLLEET LVIFTADNGP ETMRMSRGGC SGLLRCGKGT TYEGGVREPA LAFWPGHIAP
GVTHELASSL DLLPTLAALA GAPLPSVTLD GFDLSPLLLG TGKSPRQSLF FYPSYPDEVR
GVFAVRTGKY KAHFFTQGSA HSDTTADPAC HASSSLTAHE PPLLYDLSKD PGENYNLLGG
VAGATPEVLQ ALKQLQLLKA QLDAAVTFGP SQVARGEDPA LQICCHPGCT PRPACCHCPD
PHA*
speed 1.44 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
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