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 4 transcript(s)...
Querying Taster for transcript #1: ENST00000328724
Querying Taster for transcript #2: ENST00000350249
Querying Taster for transcript #3: ENST00000334743
Querying Taster for transcript #4: ENST00000422945
MT speed 0 s - this script 4.683324 s

Results

genesymbolpredictionprobabilitymodelprediction
problem		splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
PPP2R5Cpolymorphism_automatic0.999999726879692simple_aaeaffectedA531Psingle base exchangers3742424show file
PPP2R5Cpolymorphism_automatic0.999999726879692simple_aaeaffectedA476Psingle base exchangers3742424show file
PPP2R5Cpolymorphism_automatic0.999999883017421simple_aaeaffectedA515Psingle base exchangers3742424show file
PPP2R5Cpolymorphism_automatic0.999999883017421simple_aaeaffectedA546Psingle base exchangers3742424show file

Taster files

Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 2.73120308434437e-07 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr14:102391577G>CN/A show variant in all transcripts   IGV
HGNC symbol PPP2R5C
Ensembl transcript ID ENST00000328724
Genbank transcript ID NM_001161726
UniProt peptide Q13362
alteration type single base exchange
alteration region CDS
DNA changes c.1591G>C
cDNA.1600G>C
g.163443G>C
AA changes A531P Score: 27 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 531
frameshift no
known variant Reference ID: rs3742424
databasehomozygous (C/C)heterozygousallele carriers
1000G101683784
ExAC11571093112088
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.4071
5.6581
(flanking)4.0291
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 increased163441wt: 0.4576 / mu: 0.4785 (marginal change - not scored)wt: AGCCTTGGAAGCTCACTGCAGGGCCGATGAGCTGGCCTCCC
mu: AGCCTTGGAAGCTCACTGCAGGCCCGATGAGCTGGCCTCCC		 gcag|GGCC
Donor increased163435wt: 0.53 / mu: 0.62wt: AGCTCACTGCAGGGC
mu: AGCTCACTGCAGGCC		 CTCA|ctgc
Donor marginally increased163445wt: 0.8893 / mu: 0.9617 (marginal change - not scored)wt: AGGGCCGATGAGCTG
mu: AGGCCCGATGAGCTG		 GGCC|gatg
Donor marginally increased163440wt: 0.6417 / mu: 0.6782 (marginal change - not scored)wt: ACTGCAGGGCCGATG
mu: ACTGCAGGCCCGATG		 TGCA|gggc
distance from splice site 100
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      531HTKKALEAHCRADELASQDGR*
mutated  not conserved    531HTKKALEAHCRPDELASQDGR
Ptroglodytes  all identical  ENSPTRG00000006734  537HTKKALEAHCRADELASQDGR
Mmulatta  all identical  ENSMMUG00000000186  530HTKKALEAHCRADELASQDGR
Fcatus  all identical  ENSFCAG00000008937  522HTKNALEAHCRADQ
Mmusculus  all identical  ENSMUSG00000017843  515HTEKALEAHCRASELLSQDGR
Ggallus  all identical  ENSGALG00000011260  569YTMKALESHCRADELISHDG
Trubripes  no homologue    
Drerio  no alignment  ENSDARG00000059083  n/a
Dmelanogaster  not conserved  FBgn0042693  971GTVKALNEHKRTDE
Celegans  no alignment  C13G3.3  n/a
Xtropicalis  all identical  ENSXETG00000010224  569YTMKALESHCRADELISHDG
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1623 / 1623
position (AA) of stopcodon in wt / mu AA sequence 541 / 541
position of stopcodon in wt / mu cDNA 1632 / 1632
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 10 / 10
chromosome 14
strand 1
last intron/exon boundary 1501
theoretical NMD boundary in CDS 1441
length of CDS 1623
coding sequence (CDS) position 1591
cDNA position
(for ins/del: last normal base / first normal base)		 1600
gDNA position
(for ins/del: last normal base / first normal base)		 163443
chromosomal position
(for ins/del: last normal base / first normal base)		 102391577
original gDNA sequence snippet CCTTGGAAGCTCACTGCAGGGCCGATGAGCTGGCCTCCCAG
altered gDNA sequence snippet CCTTGGAAGCTCACTGCAGGCCCGATGAGCTGGCCTCCCAG
original cDNA sequence snippet CCTTGGAAGCTCACTGCAGGGCCGATGAGCTGGCCTCCCAG
altered cDNA sequence snippet CCTTGGAAGCTCACTGCAGGCCCGATGAGCTGGCCTCCCAG
wildtype AA sequence MPNKNKKEKE SPKAGKSGKS SKEGQDTVES EQISVRKNSL VAVPSTVSAK IKVPVSQPIV
KKDKRQNSSR FSASNNRELQ KLPSLKDVPP ADQEKLFIQK LRQCCVLFDF VSDPLSDLKW
KEVKRAALSE MVEYITHNRN VITEPIYPEV VHMFAVNMFR TLPPSSNPTG AEFDPEEDEP
TLEAAWPHLQ LVYEFFLRFL ESPDFQPNIA KKYIDQKFVL QLLELFDSED PRERDFLKTT
LHRIYGKFLG LRAYIRKQIN NIFYRFIYET EHHNGIAELL EILGSIINGF ALPLKEEHKI
FLLKVLLPLH KVKSLSVYHP QLAYCVVQFL EKDSTLTEPV VMALLKYWPK THSPKEVMFL
NELEEILDVI EPSEFVKIME PLFRQLAKCV SSPHFQVAER ALYYWNNEYI MSLISDNAAK
ILPIMFPSLY RNSKTHWNKT IHGLIYNALK LFMEMNQKLF DDCTQQFKAE KLKEKLKMKE
REEAWVKIEN LAKANPQAQK DPKKDRPLAR RKSELPQDPH TKKALEAHCR ADELASQDGR
*
mutated AA sequence MPNKNKKEKE SPKAGKSGKS SKEGQDTVES EQISVRKNSL VAVPSTVSAK IKVPVSQPIV
KKDKRQNSSR FSASNNRELQ KLPSLKDVPP ADQEKLFIQK LRQCCVLFDF VSDPLSDLKW
KEVKRAALSE MVEYITHNRN VITEPIYPEV VHMFAVNMFR TLPPSSNPTG AEFDPEEDEP
TLEAAWPHLQ LVYEFFLRFL ESPDFQPNIA KKYIDQKFVL QLLELFDSED PRERDFLKTT
LHRIYGKFLG LRAYIRKQIN NIFYRFIYET EHHNGIAELL EILGSIINGF ALPLKEEHKI
FLLKVLLPLH KVKSLSVYHP QLAYCVVQFL EKDSTLTEPV VMALLKYWPK THSPKEVMFL
NELEEILDVI EPSEFVKIME PLFRQLAKCV SSPHFQVAER ALYYWNNEYI MSLISDNAAK
ILPIMFPSLY RNSKTHWNKT IHGLIYNALK LFMEMNQKLF DDCTQQFKAE KLKEKLKMKE
REEAWVKIEN LAKANPQAQK DPKKDRPLAR RKSELPQDPH TKKALEAHCR PDELASQDGR
*
speed 1.19 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: 2.73120308434437e-07 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr14:102391577G>CN/A show variant in all transcripts   IGV
HGNC symbol PPP2R5C
Ensembl transcript ID ENST00000350249
Genbank transcript ID NM_178586
UniProt peptide Q13362
alteration type single base exchange
alteration region CDS
DNA changes c.1426G>C
cDNA.1566G>C
g.163443G>C
AA changes A476P Score: 27 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 476
frameshift no
known variant Reference ID: rs3742424
databasehomozygous (C/C)heterozygousallele carriers
1000G101683784
ExAC11571093112088
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.4071
5.6581
(flanking)4.0291
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 increased163441wt: 0.4576 / mu: 0.4785 (marginal change - not scored)wt: AGCCTTGGAAGCTCACTGCAGGGCCGATGAGCTGGCCTCCC
mu: AGCCTTGGAAGCTCACTGCAGGCCCGATGAGCTGGCCTCCC		 gcag|GGCC
Donor increased163435wt: 0.53 / mu: 0.62wt: AGCTCACTGCAGGGC
mu: AGCTCACTGCAGGCC		 CTCA|ctgc
Donor marginally increased163445wt: 0.8893 / mu: 0.9617 (marginal change - not scored)wt: AGGGCCGATGAGCTG
mu: AGGCCCGATGAGCTG		 GGCC|gatg
Donor marginally increased163440wt: 0.6417 / mu: 0.6782 (marginal change - not scored)wt: ACTGCAGGGCCGATG
mu: ACTGCAGGCCCGATG		 TGCA|gggc
distance from splice site 100
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      476HTKKALEAHCRADELASQDGR*
mutated  not conserved    476HTKKALEAHCRPDELA
Ptroglodytes  all identical  ENSPTRG00000006734  537AHCRADELASQDGR
Mmulatta  all identical  ENSMMUG00000000186  530HTKKALEAHCRADELASQDGR
Fcatus  all identical  ENSFCAG00000008937  522HTKNALEAHCRADQ
Mmusculus  all identical  ENSMUSG00000017843  515HTEKALEAHCRASELLSQDGR
Ggallus  all identical  ENSGALG00000011260  569LESHCRADELISHDG
Trubripes  no homologue    
Drerio  no alignment  ENSDARG00000059083  n/a
Dmelanogaster  not conserved  FBgn0042693  971GTVKALNEHKRTDE
Celegans  no alignment  C13G3.3  n/a
Xtropicalis  all identical  ENSXETG00000010224  569LESHCRADELISHDG
protein features
start (aa)end (aa)featuredetails 
494494CONFLICTR -> L (in Ref. 1; AAC50387).might get lost (downstream of altered splice site)
497497MOD_RESPhosphoserine (By similarity).might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1458 / 1458
position (AA) of stopcodon in wt / mu AA sequence 486 / 486
position of stopcodon in wt / mu cDNA 1598 / 1598
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 141 / 141
chromosome 14
strand 1
last intron/exon boundary 1467
theoretical NMD boundary in CDS 1276
length of CDS 1458
coding sequence (CDS) position 1426
cDNA position
(for ins/del: last normal base / first normal base)		 1566
gDNA position
(for ins/del: last normal base / first normal base)		 163443
chromosomal position
(for ins/del: last normal base / first normal base)		 102391577
original gDNA sequence snippet CCTTGGAAGCTCACTGCAGGGCCGATGAGCTGGCCTCCCAG
altered gDNA sequence snippet CCTTGGAAGCTCACTGCAGGCCCGATGAGCTGGCCTCCCAG
original cDNA sequence snippet CCTTGGAAGCTCACTGCAGGGCCGATGAGCTGGCCTCCCAG
altered cDNA sequence snippet CCTTGGAAGCTCACTGCAGGCCCGATGAGCTGGCCTCCCAG
wildtype AA sequence MLTCNKAGSR MVVDAANSNG PFQPVVLLHI RDVPPADQEK LFIQKLRQCC VLFDFVSDPL
SDLKWKEVKR AALSEMVEYI THNRNVITEP IYPEVVHMFA VNMFRTLPPS SNPTGAEFDP
EEDEPTLEAA WPHLQLVYEF FLRFLESPDF QPNIAKKYID QKFVLQLLEL FDSEDPRERD
FLKTTLHRIY GKFLGLRAYI RKQINNIFYR FIYETEHHNG IAELLEILGS IINGFALPLK
EEHKIFLLKV LLPLHKVKSL SVYHPQLAYC VVQFLEKDST LTEPVVMALL KYWPKTHSPK
EVMFLNELEE ILDVIEPSEF VKIMEPLFRQ LAKCVSSPHF QVAERALYYW NNEYIMSLIS
DNAAKILPIM FPSLYRNSKT HWNKTIHGLI YNALKLFMEM NQKLFDDCTQ QFKAEKLKEK
LKMKEREEAW VKIENLAKAN PQAQKDPKKD RPLARRKSEL PQDPHTKKAL EAHCRADELA
SQDGR*
mutated AA sequence MLTCNKAGSR MVVDAANSNG PFQPVVLLHI RDVPPADQEK LFIQKLRQCC VLFDFVSDPL
SDLKWKEVKR AALSEMVEYI THNRNVITEP IYPEVVHMFA VNMFRTLPPS SNPTGAEFDP
EEDEPTLEAA WPHLQLVYEF FLRFLESPDF QPNIAKKYID QKFVLQLLEL FDSEDPRERD
FLKTTLHRIY GKFLGLRAYI RKQINNIFYR FIYETEHHNG IAELLEILGS IINGFALPLK
EEHKIFLLKV LLPLHKVKSL SVYHPQLAYC VVQFLEKDST LTEPVVMALL KYWPKTHSPK
EVMFLNELEE ILDVIEPSEF VKIMEPLFRQ LAKCVSSPHF QVAERALYYW NNEYIMSLIS
DNAAKILPIM FPSLYRNSKT HWNKTIHGLI YNALKLFMEM NQKLFDDCTQ QFKAEKLKEK
LKMKEREEAW VKIENLAKAN PQAQKDPKKD RPLARRKSEL PQDPHTKKAL EAHCRPDELA
SQDGR*
speed 1.26 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: 1.16982578701968e-07 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr14:102391577G>CN/A show variant in all transcripts   IGV
HGNC symbol PPP2R5C
Ensembl transcript ID ENST00000334743
Genbank transcript ID NM_002719
UniProt peptide Q13362
alteration type single base exchange
alteration region CDS
DNA changes c.1543G>C
cDNA.1591G>C
g.163443G>C
AA changes A515P Score: 27 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 515
frameshift no
known variant Reference ID: rs3742424
databasehomozygous (C/C)heterozygousallele carriers
1000G101683784
ExAC11571093112088
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.4071
5.6581
(flanking)4.0291
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 increased163441wt: 0.4576 / mu: 0.4785 (marginal change - not scored)wt: AGCCTTGGAAGCTCACTGCAGGGCCGATGAGCTGGCCTCCC
mu: AGCCTTGGAAGCTCACTGCAGGCCCGATGAGCTGGCCTCCC		 gcag|GGCC
Donor increased163435wt: 0.53 / mu: 0.62wt: AGCTCACTGCAGGGC
mu: AGCTCACTGCAGGCC		 CTCA|ctgc
Donor marginally increased163445wt: 0.8893 / mu: 0.9617 (marginal change - not scored)wt: AGGGCCGATGAGCTG
mu: AGGCCCGATGAGCTG		 GGCC|gatg
Donor marginally increased163440wt: 0.6417 / mu: 0.6782 (marginal change - not scored)wt: ACTGCAGGGCCGATG
mu: ACTGCAGGCCCGATG		 TGCA|gggc
distance from splice site 100
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      515HTKKALEAHCRADELASQDGR*
mutated  not conserved    515HTKKALEAHCRPDELASQDGR
Ptroglodytes  all identical  ENSPTRG00000006734  537AHCRADELASQDGR
Mmulatta  all identical  ENSMMUG00000000186  530HTKKALEAHCRADELASQDGR
Fcatus  all identical  ENSFCAG00000008937  525HTKNALEAHCRADQLVSQDGR
Mmusculus  all identical  ENSMUSG00000017843  515HTEKALEAHCRASELLSQDGR
Ggallus  all identical  ENSGALG00000011260  569LESHCRADELISHDG
Trubripes  no homologue    
Drerio  no alignment  ENSDARG00000059083  n/a
Dmelanogaster  not conserved  FBgn0042693  971GTVKALNEHKRTDE
Celegans  not conserved  C13G3.3  594QTTRALGEYKRHD
Xtropicalis  all identical  ENSXETG00000010224  569LESHCRADELISHDG
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1575 / 1575
position (AA) of stopcodon in wt / mu AA sequence 525 / 525
position of stopcodon in wt / mu cDNA 1623 / 1623
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 49 / 49
chromosome 14
strand 1
last intron/exon boundary 1492
theoretical NMD boundary in CDS 1393
length of CDS 1575
coding sequence (CDS) position 1543
cDNA position
(for ins/del: last normal base / first normal base)		 1591
gDNA position
(for ins/del: last normal base / first normal base)		 163443
chromosomal position
(for ins/del: last normal base / first normal base)		 102391577
original gDNA sequence snippet CCTTGGAAGCTCACTGCAGGGCCGATGAGCTGGCCTCCCAG
altered gDNA sequence snippet CCTTGGAAGCTCACTGCAGGCCCGATGAGCTGGCCTCCCAG
original cDNA sequence snippet CCTTGGAAGCTCACTGCAGGGCCGATGAGCTGGCCTCCCAG
altered cDNA sequence snippet CCTTGGAAGCTCACTGCAGGCCCGATGAGCTGGCCTCCCAG
wildtype AA sequence MLTCNKAGSR MVVDAANSNG PFQPVVLLHI RDVPPADQEK LFIQKLRQCC VLFDFVSDPL
SDLKWKEVKR AALSEMVEYI THNRNVITEP IYPEVVHMFA VNMFRTLPPS SNPTGAEFDP
EEDEPTLEAA WPHLQLVYEF FLRFLESPDF QPNIAKKYID QKFVLQLLEL FDSEDPRERD
FLKTTLHRIY GKFLGLRAYI RKQINNIFYR FIYETEHHNG IAELLEILGS IINGFALPLK
EEHKIFLLKV LLPLHKVKSL SVYHPQLAYC VVQFLEKDST LTEPVVMALL KYWPKTHSPK
EVMFLNELEE ILDVIEPSEF VKIMEPLFRQ LAKCVSSPHF QVAERALYYW NNEYIMSLIS
DNAAKILPIM FPSLYRNSKT HWNKTIHGLI YNALKLFMEM NQKLFDDCTQ QFKAEKLKEK
LKMKEREEAW VKIENLAKAN PQYTVYSQAS TMSIPVAMET DGPLFEDVQM LRKTVKDEAH
QAQKDPKKDR PLARRKSELP QDPHTKKALE AHCRADELAS QDGR*
mutated AA sequence MLTCNKAGSR MVVDAANSNG PFQPVVLLHI RDVPPADQEK LFIQKLRQCC VLFDFVSDPL
SDLKWKEVKR AALSEMVEYI THNRNVITEP IYPEVVHMFA VNMFRTLPPS SNPTGAEFDP
EEDEPTLEAA WPHLQLVYEF FLRFLESPDF QPNIAKKYID QKFVLQLLEL FDSEDPRERD
FLKTTLHRIY GKFLGLRAYI RKQINNIFYR FIYETEHHNG IAELLEILGS IINGFALPLK
EEHKIFLLKV LLPLHKVKSL SVYHPQLAYC VVQFLEKDST LTEPVVMALL KYWPKTHSPK
EVMFLNELEE ILDVIEPSEF VKIMEPLFRQ LAKCVSSPHF QVAERALYYW NNEYIMSLIS
DNAAKILPIM FPSLYRNSKT HWNKTIHGLI YNALKLFMEM NQKLFDDCTQ QFKAEKLKEK
LKMKEREEAW VKIENLAKAN PQYTVYSQAS TMSIPVAMET DGPLFEDVQM LRKTVKDEAH
QAQKDPKKDR PLARRKSELP QDPHTKKALE AHCRPDELAS QDGR*
speed 1.15 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: 1.16982578701968e-07 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr14:102391577G>CN/A show variant in all transcripts   IGV
HGNC symbol PPP2R5C
Ensembl transcript ID ENST00000422945
Genbank transcript ID NM_001161725
UniProt peptide Q13362
alteration type single base exchange
alteration region CDS
DNA changes c.1636G>C
cDNA.1732G>C
g.163443G>C
AA changes A546P Score: 27 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 546
frameshift no
known variant Reference ID: rs3742424
databasehomozygous (C/C)heterozygousallele carriers
1000G101683784
ExAC11571093112088
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.4071
5.6581
(flanking)4.0291
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 increased163441wt: 0.4576 / mu: 0.4785 (marginal change - not scored)wt: AGCCTTGGAAGCTCACTGCAGGGCCGATGAGCTGGCCTCCC
mu: AGCCTTGGAAGCTCACTGCAGGCCCGATGAGCTGGCCTCCC		 gcag|GGCC
Donor increased163435wt: 0.53 / mu: 0.62wt: AGCTCACTGCAGGGC
mu: AGCTCACTGCAGGCC		 CTCA|ctgc
Donor marginally increased163445wt: 0.8893 / mu: 0.9617 (marginal change - not scored)wt: AGGGCCGATGAGCTG
mu: AGGCCCGATGAGCTG		 GGCC|gatg
Donor marginally increased163440wt: 0.6417 / mu: 0.6782 (marginal change - not scored)wt: ACTGCAGGGCCGATG
mu: ACTGCAGGCCCGATG		 TGCA|gggc
distance from splice site 100
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      546HTKKALEAHCRADELASQDGR*
mutated  not conserved    546EAHCRPDELASQDGR
Ptroglodytes  all identical  ENSPTRG00000006734  537HTKKALEAHCRADEL
Mmulatta  all identical  ENSMMUG00000000186  530HTKKALEAHCRADELASQDGR
Fcatus  all identical  ENSFCAG00000008937  525HTKNALEAHCRADQLVSQDGR
Mmusculus  all identical  ENSMUSG00000017843  515AHCRASELLSQDGR
Ggallus  all identical  ENSGALG00000011260  569YTMKALESHCRADELISHDG
Trubripes  no homologue    
Drerio  no alignment  ENSDARG00000059083  n/a
Dmelanogaster  not conserved  FBgn0042693  971GTVKALNEHKRTDE
Celegans  not conserved  C13G3.3  594QTTRALGEYKRHD
Xtropicalis  all identical  ENSXETG00000010224  569YTMKALESHCRADELISHDG
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1668 / 1668
position (AA) of stopcodon in wt / mu AA sequence 556 / 556
position of stopcodon in wt / mu cDNA 1764 / 1764
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 97 / 97
chromosome 14
strand 1
last intron/exon boundary 1633
theoretical NMD boundary in CDS 1486
length of CDS 1668
coding sequence (CDS) position 1636
cDNA position
(for ins/del: last normal base / first normal base)		 1732
gDNA position
(for ins/del: last normal base / first normal base)		 163443
chromosomal position
(for ins/del: last normal base / first normal base)		 102391577
original gDNA sequence snippet CCTTGGAAGCTCACTGCAGGGCCGATGAGCTGGCCTCCCAG
altered gDNA sequence snippet CCTTGGAAGCTCACTGCAGGCCCGATGAGCTGGCCTCCCAG
original cDNA sequence snippet CCTTGGAAGCTCACTGCAGGGCCGATGAGCTGGCCTCCCAG
altered cDNA sequence snippet CCTTGGAAGCTCACTGCAGGCCCGATGAGCTGGCCTCCCAG
wildtype AA sequence MPNKNKKEKE SPKAGKSGKS SKEGQDTVES EGTSPEEPSS PKVPPPLLPE LLVLIFGGLQ
GRDVPPADQE KLFIQKLRQC CVLFDFVSDP LSDLKWKEVK RAALSEMVEY ITHNRNVITE
PIYPEVVHMF AVNMFRTLPP SSNPTGAEFD PEEDEPTLEA AWPHLQLVYE FFLRFLESPD
FQPNIAKKYI DQKFVLQLLE LFDSEDPRER DFLKTTLHRI YGKFLGLRAY IRKQINNIFY
RFIYETEHHN GIAELLEILG SIINGFALPL KEEHKIFLLK VLLPLHKVKS LSVYHPQLAY
CVVQFLEKDS TLTEPVVMAL LKYWPKTHSP KEVMFLNELE EILDVIEPSE FVKIMEPLFR
QLAKCVSSPH FQVAERALYY WNNEYIMSLI SDNAAKILPI MFPSLYRNSK THWNKTIHGL
IYNALKLFME MNQKLFDDCT QQFKAEKLKE KLKMKEREEA WVKIENLAKA NPQYTVYSQA
STMSIPVAME TDGPLFEDVQ MLRKTVKDEA HQAQKDPKKD RPLARRKSEL PQDPHTKKAL
EAHCRADELA SQDGR*
mutated AA sequence MPNKNKKEKE SPKAGKSGKS SKEGQDTVES EGTSPEEPSS PKVPPPLLPE LLVLIFGGLQ
GRDVPPADQE KLFIQKLRQC CVLFDFVSDP LSDLKWKEVK RAALSEMVEY ITHNRNVITE
PIYPEVVHMF AVNMFRTLPP SSNPTGAEFD PEEDEPTLEA AWPHLQLVYE FFLRFLESPD
FQPNIAKKYI DQKFVLQLLE LFDSEDPRER DFLKTTLHRI YGKFLGLRAY IRKQINNIFY
RFIYETEHHN GIAELLEILG SIINGFALPL KEEHKIFLLK VLLPLHKVKS LSVYHPQLAY
CVVQFLEKDS TLTEPVVMAL LKYWPKTHSP KEVMFLNELE EILDVIEPSE FVKIMEPLFR
QLAKCVSSPH FQVAERALYY WNNEYIMSLI SDNAAKILPI MFPSLYRNSK THWNKTIHGL
IYNALKLFME MNQKLFDDCT QQFKAEKLKE KLKMKEREEA WVKIENLAKA NPQYTVYSQA
STMSIPVAME TDGPLFEDVQ MLRKTVKDEA HQAQKDPKKD RPLARRKSEL PQDPHTKKAL
EAHCRPDELA SQDGR*
speed 0.96 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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Problems