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: ENST00000400237
Querying Taster for transcript #2: ENST00000248980
Querying Taster for transcript #3: ENST00000248983
Querying Taster for transcript #4: ENST00000400236
MT speed 5.82 s - this script 6.967116 s

Results


genesymbolpredictionprobabilitymodelprediction
problem
splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
RFPL2polymorphism_automatic9.99200722162641e-16simple_aaeaffectedV287Isingle base exchangers136467show file
RFPL2polymorphism_automatic9.99200722162641e-16simple_aaeaffectedV348Isingle base exchangers136467show file
RFPL2polymorphism_automatic9.99200722162641e-16simple_aaeaffectedV258Isingle base exchangers136467show file
RFPL2polymorphism_automatic9.99200722162641e-16simple_aaeaffectedV258Isingle base exchangers136467show file

Taster files

Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: simple_aae, prob: 0.999999999999999 (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) chr22:32586854C>TN/A show variant in all transcripts   IGV
HGNC symbol RFPL2
Ensembl transcript ID ENST00000248980
Genbank transcript ID NM_006605
UniProt peptide O75678
alteration type single base exchange
alteration region CDS
DNA changes c.859G>A
cDNA.1064G>A
g.13865G>A
AA changes V287I Score: 29 explain score(s)
position(s) of altered AA
if AA alteration in CDS
287
frameshift no
known variant Reference ID: rs136467
databasehomozygous (T/T)heterozygousallele carriers
1000G6919811672
ExAC11441988521326
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.1250
-3.0510
(flanking)-0.4610.007
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased13868wt: 0.68 / mu: 0.83wt: CATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGT
mu: CATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGT
 gttc|CACC
Acc increased13871wt: 0.23 / mu: 0.25wt: TTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGTGTC
mu: TTTTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGTGTC
 ccac|CTAA
Acc marginally increased13873wt: 0.5920 / mu: 0.6064 (marginal change - not scored)wt: TTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGTGTCTT
mu: TTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGTGTCTT
 acct|AATG
Acc increased13869wt: 0.51 / mu: 0.61wt: ATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGTG
mu: ATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGTG
 ttcc|ACCT
Acc marginally increased13865wt: 0.8409 / mu: 0.8632 (marginal change - not scored)wt: GCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAA
mu: GCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAA
 tcag|TTCC
Acc marginally increased13860wt: 0.2945 / mu: 0.3144 (marginal change - not scored)wt: ATTGCGCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTG
mu: ATTGCGCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTG
 ctcc|TTCA
Donor increased13870wt: 0.22 / mu: 0.27wt: GTTCCACCTAATGGT
mu: ATTCCACCTAATGGT
 TCCA|ccta
Donor gained138600.71mu: GGCTCCTTCAATTCC CTCC|ttca
distance from splice site 433
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      287EEPLRPFLAPSVPPNGDQGVLSIC
mutated  all conserved    287EEPLRPFLAPSIPPNGDQGVLSI
Ptroglodytes  all conserved  ENSPTRG00000014283  348EEPLRPFLAPSIPPNGDQGVLSI
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
168362DOMAINB30.2/SPRY.lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 954 / 954
position (AA) of stopcodon in wt / mu AA sequence 318 / 318
position of stopcodon in wt / mu cDNA 1159 / 1159
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 206 / 206
chromosome 22
strand -1
last intron/exon boundary 579
theoretical NMD boundary in CDS 323
length of CDS 954
coding sequence (CDS) position 859
cDNA position
(for ins/del: last normal base / first normal base)
1064
gDNA position
(for ins/del: last normal base / first normal base)
13865
chromosomal position
(for ins/del: last normal base / first normal base)
32586854
original gDNA sequence snippet GCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAA
altered gDNA sequence snippet GCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAA
original cDNA sequence snippet GCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAA
altered cDNA sequence snippet GCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAA
wildtype AA sequence MKRLSLVTTN RLSPHGNFFT LCTFPLAVDM AALFQEASSC PVCSDYLEKP MSLECGCAVC
LKCINSLQKE PHGEDLLCCC SSMVSRKNKI RRNRQLERLA SHIKELEPKL KKILQMNPRM
RKFQVDMTLD ANTANNFLLI SDDLRSVRSG RIRQNRQDLA ERFDVSVCIL GSPRFTCGRH
CWEVDVGTST EWDLGVCRES VHRKGRIQLT TELGFWTVSL RDGGRLSATT VPLTFLFVDR
KLQRVGIFLD MGMQNVSFFD AESGSHVYTF RSVSAEEPLR PFLAPSVPPN GDQGVLSICP
LMNSGTTDAP VRPGEAK*
mutated AA sequence MKRLSLVTTN RLSPHGNFFT LCTFPLAVDM AALFQEASSC PVCSDYLEKP MSLECGCAVC
LKCINSLQKE PHGEDLLCCC SSMVSRKNKI RRNRQLERLA SHIKELEPKL KKILQMNPRM
RKFQVDMTLD ANTANNFLLI SDDLRSVRSG RIRQNRQDLA ERFDVSVCIL GSPRFTCGRH
CWEVDVGTST EWDLGVCRES VHRKGRIQLT TELGFWTVSL RDGGRLSATT VPLTFLFVDR
KLQRVGIFLD MGMQNVSFFD AESGSHVYTF RSVSAEEPLR PFLAPSIPPN GDQGVLSICP
LMNSGTTDAP VRPGEAK*
speed 1.08 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: 0.999999999999999 (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) chr22:32586854C>TN/A show variant in all transcripts   IGV
HGNC symbol RFPL2
Ensembl transcript ID ENST00000400237
Genbank transcript ID NM_001098527
UniProt peptide O75678
alteration type single base exchange
alteration region CDS
DNA changes c.1042G>A
cDNA.1978G>A
g.13865G>A
AA changes V348I Score: 29 explain score(s)
position(s) of altered AA
if AA alteration in CDS
348
frameshift no
known variant Reference ID: rs136467
databasehomozygous (T/T)heterozygousallele carriers
1000G6919811672
ExAC11441988521326
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.1250
-3.0510
(flanking)-0.4610.007
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased13868wt: 0.68 / mu: 0.83wt: CATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGT
mu: CATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGT
 gttc|CACC
Acc increased13871wt: 0.23 / mu: 0.25wt: TTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGTGTC
mu: TTTTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGTGTC
 ccac|CTAA
Acc marginally increased13873wt: 0.5920 / mu: 0.6064 (marginal change - not scored)wt: TTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGTGTCTT
mu: TTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGTGTCTT
 acct|AATG
Acc increased13869wt: 0.51 / mu: 0.61wt: ATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGTG
mu: ATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGTG
 ttcc|ACCT
Acc marginally increased13865wt: 0.8409 / mu: 0.8632 (marginal change - not scored)wt: GCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAA
mu: GCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAA
 tcag|TTCC
Acc marginally increased13860wt: 0.2945 / mu: 0.3144 (marginal change - not scored)wt: ATTGCGCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTG
mu: ATTGCGCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTG
 ctcc|TTCA
Donor increased13870wt: 0.22 / mu: 0.27wt: GTTCCACCTAATGGT
mu: ATTCCACCTAATGGT
 TCCA|ccta
Donor gained138600.71mu: GGCTCCTTCAATTCC CTCC|ttca
distance from splice site 430
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      348EEPLRPFLAPSVPPNGDQGVLSIC
mutated  all conserved    348EEPLRPFLAPSIPPNGDQGVLSI
Ptroglodytes  all conserved  ENSPTRG00000014283  348EEPLRPFLAPSIPPNGDQGVLSI
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
168362DOMAINB30.2/SPRY.lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1137 / 1137
position (AA) of stopcodon in wt / mu AA sequence 379 / 379
position of stopcodon in wt / mu cDNA 2073 / 2073
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 937 / 937
chromosome 22
strand -1
last intron/exon boundary 1493
theoretical NMD boundary in CDS 506
length of CDS 1137
coding sequence (CDS) position 1042
cDNA position
(for ins/del: last normal base / first normal base)
1978
gDNA position
(for ins/del: last normal base / first normal base)
13865
chromosomal position
(for ins/del: last normal base / first normal base)
32586854
original gDNA sequence snippet GCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAA
altered gDNA sequence snippet GCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAA
original cDNA sequence snippet GCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAA
altered cDNA sequence snippet GCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAA
wildtype AA sequence MEVAELGFPE TAVSQSRICL CAVLCGHWDF ADMMVIRSLS LIRLEGVEGR DPVGGGNLTN
KRPSCAPSPQ DLSAQWKQLE DRGASSRRVD MAALFQEASS CPVCSDYLEK PMSLECGCAV
CLKCINSLQK EPHGEDLLCC CSSMVSRKNK IRRNRQLERL ASHIKELEPK LKKILQMNPR
MRKFQVDMTL DANTANNFLL ISDDLRSVRS GRIRQNRQDL AERFDVSVCI LGSPRFTCGR
HCWEVDVGTS TEWDLGVCRE SVHRKGRIQL TTELGFWTVS LRDGGRLSAT TVPLTFLFVD
RKLQRVGIFL DMGMQNVSFF DAESGSHVYT FRSVSAEEPL RPFLAPSVPP NGDQGVLSIC
PLMNSGTTDA PVRPGEAK*
mutated AA sequence MEVAELGFPE TAVSQSRICL CAVLCGHWDF ADMMVIRSLS LIRLEGVEGR DPVGGGNLTN
KRPSCAPSPQ DLSAQWKQLE DRGASSRRVD MAALFQEASS CPVCSDYLEK PMSLECGCAV
CLKCINSLQK EPHGEDLLCC CSSMVSRKNK IRRNRQLERL ASHIKELEPK LKKILQMNPR
MRKFQVDMTL DANTANNFLL ISDDLRSVRS GRIRQNRQDL AERFDVSVCI LGSPRFTCGR
HCWEVDVGTS TEWDLGVCRE SVHRKGRIQL TTELGFWTVS LRDGGRLSAT TVPLTFLFVD
RKLQRVGIFL DMGMQNVSFF DAESGSHVYT FRSVSAEEPL RPFLAPSIPP NGDQGVLSIC
PLMNSGTTDA PVRPGEAK*
speed 1.01 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: 0.999999999999999 (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) chr22:32586854C>TN/A show variant in all transcripts   IGV
HGNC symbol RFPL2
Ensembl transcript ID ENST00000400236
Genbank transcript ID N/A
UniProt peptide O75678
alteration type single base exchange
alteration region CDS
DNA changes c.772G>A
cDNA.1978G>A
g.13865G>A
AA changes V258I Score: 29 explain score(s)
position(s) of altered AA
if AA alteration in CDS
258
frameshift no
known variant Reference ID: rs136467
databasehomozygous (T/T)heterozygousallele carriers
1000G6919811672
ExAC11441988521326
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.1250
-3.0510
(flanking)-0.4610.007
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased13868wt: 0.68 / mu: 0.83wt: CATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGT
mu: CATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGT
 gttc|CACC
Acc increased13871wt: 0.23 / mu: 0.25wt: TTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGTGTC
mu: TTTTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGTGTC
 ccac|CTAA
Acc marginally increased13873wt: 0.5920 / mu: 0.6064 (marginal change - not scored)wt: TTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGTGTCTT
mu: TTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGTGTCTT
 acct|AATG
Acc increased13869wt: 0.51 / mu: 0.61wt: ATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGTG
mu: ATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGTG
 ttcc|ACCT
Acc marginally increased13865wt: 0.8409 / mu: 0.8632 (marginal change - not scored)wt: GCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAA
mu: GCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAA
 tcag|TTCC
Acc marginally increased13860wt: 0.2945 / mu: 0.3144 (marginal change - not scored)wt: ATTGCGCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTG
mu: ATTGCGCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTG
 ctcc|TTCA
Donor increased13870wt: 0.22 / mu: 0.27wt: GTTCCACCTAATGGT
mu: ATTCCACCTAATGGT
 TCCA|ccta
Donor gained138600.71mu: GGCTCCTTCAATTCC CTCC|ttca
distance from splice site 433
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      258EEPLRPFLAPSVPPNGDQGVLSIC
mutated  all conserved    258EEPLRPFLAPSIPPNGDQGVLSI
Ptroglodytes  all conserved  ENSPTRG00000014283  348EEPLRPFLAPSIPPNGDQGVLSI
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
168362DOMAINB30.2/SPRY.lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 867 / 867
position (AA) of stopcodon in wt / mu AA sequence 289 / 289
position of stopcodon in wt / mu cDNA 2073 / 2073
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 1207 / 1207
chromosome 22
strand -1
last intron/exon boundary 1493
theoretical NMD boundary in CDS 236
length of CDS 867
coding sequence (CDS) position 772
cDNA position
(for ins/del: last normal base / first normal base)
1978
gDNA position
(for ins/del: last normal base / first normal base)
13865
chromosomal position
(for ins/del: last normal base / first normal base)
32586854
original gDNA sequence snippet GCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAA
altered gDNA sequence snippet GCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAA
original cDNA sequence snippet GCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAA
altered cDNA sequence snippet GCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAA
wildtype AA sequence MAALFQEASS CPVCSDYLEK PMSLECGCAV CLKCINSLQK EPHGEDLLCC CSSMVSRKNK
IRRNRQLERL ASHIKELEPK LKKILQMNPR MRKFQVDMTL DANTANNFLL ISDDLRSVRS
GRIRQNRQDL AERFDVSVCI LGSPRFTCGR HCWEVDVGTS TEWDLGVCRE SVHRKGRIQL
TTELGFWTVS LRDGGRLSAT TVPLTFLFVD RKLQRVGIFL DMGMQNVSFF DAESGSHVYT
FRSVSAEEPL RPFLAPSVPP NGDQGVLSIC PLMNSGTTDA PVRPGEAK*
mutated AA sequence MAALFQEASS CPVCSDYLEK PMSLECGCAV CLKCINSLQK EPHGEDLLCC CSSMVSRKNK
IRRNRQLERL ASHIKELEPK LKKILQMNPR MRKFQVDMTL DANTANNFLL ISDDLRSVRS
GRIRQNRQDL AERFDVSVCI LGSPRFTCGR HCWEVDVGTS TEWDLGVCRE SVHRKGRIQL
TTELGFWTVS LRDGGRLSAT TVPLTFLFVD RKLQRVGIFL DMGMQNVSFF DAESGSHVYT
FRSVSAEEPL RPFLAPSIPP NGDQGVLSIC PLMNSGTTDA PVRPGEAK*
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
back to results table
Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: simple_aae, prob: 0.999999999999999 (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) chr22:32586854C>TN/A show variant in all transcripts   IGV
HGNC symbol RFPL2
Ensembl transcript ID ENST00000248983
Genbank transcript ID NM_001159545
UniProt peptide O75678
alteration type single base exchange
alteration region CDS
DNA changes c.772G>A
cDNA.1020G>A
g.13865G>A
AA changes V258I Score: 29 explain score(s)
position(s) of altered AA
if AA alteration in CDS
258
frameshift no
known variant Reference ID: rs136467
databasehomozygous (T/T)heterozygousallele carriers
1000G6919811672
ExAC11441988521326
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.1250
-3.0510
(flanking)-0.4610.007
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased13868wt: 0.68 / mu: 0.83wt: CATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGT
mu: CATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGT
 gttc|CACC
Acc increased13871wt: 0.23 / mu: 0.25wt: TTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGTGTC
mu: TTTTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGTGTC
 ccac|CTAA
Acc marginally increased13873wt: 0.5920 / mu: 0.6064 (marginal change - not scored)wt: TTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGTGTCTT
mu: TTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGTGTCTT
 acct|AATG
Acc increased13869wt: 0.51 / mu: 0.61wt: ATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAAGGTG
mu: ATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAAGGTG
 ttcc|ACCT
Acc marginally increased13865wt: 0.8409 / mu: 0.8632 (marginal change - not scored)wt: GCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAA
mu: GCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAA
 tcag|TTCC
Acc marginally increased13860wt: 0.2945 / mu: 0.3144 (marginal change - not scored)wt: ATTGCGCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTG
mu: ATTGCGCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTG
 ctcc|TTCA
Donor increased13870wt: 0.22 / mu: 0.27wt: GTTCCACCTAATGGT
mu: ATTCCACCTAATGGT
 TCCA|ccta
Donor gained138600.71mu: GGCTCCTTCAATTCC CTCC|ttca
distance from splice site 433
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      258EEPLRPFLAPSVPPNGDQGVLSIC
mutated  all conserved    258EEPLRPFLAPSIPPNGDQGVLSI
Ptroglodytes  all conserved  ENSPTRG00000014283  348EEPLRPFLAPSIPPNGDQGVLSI
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
168362DOMAINB30.2/SPRY.lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 867 / 867
position (AA) of stopcodon in wt / mu AA sequence 289 / 289
position of stopcodon in wt / mu cDNA 1115 / 1115
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 249 / 249
chromosome 22
strand -1
last intron/exon boundary 535
theoretical NMD boundary in CDS 236
length of CDS 867
coding sequence (CDS) position 772
cDNA position
(for ins/del: last normal base / first normal base)
1020
gDNA position
(for ins/del: last normal base / first normal base)
13865
chromosomal position
(for ins/del: last normal base / first normal base)
32586854
original gDNA sequence snippet GCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAA
altered gDNA sequence snippet GCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAA
original cDNA sequence snippet GCCCATTTTTGGCTCCTTCAGTTCCACCTAATGGTGATCAA
altered cDNA sequence snippet GCCCATTTTTGGCTCCTTCAATTCCACCTAATGGTGATCAA
wildtype AA sequence MAALFQEASS CPVCSDYLEK PMSLECGCAV CLKCINSLQK EPHGEDLLCC CSSMVSRKNK
IRRNRQLERL ASHIKELEPK LKKILQMNPR MRKFQVDMTL DANTANNFLL ISDDLRSVRS
GRIRQNRQDL AERFDVSVCI LGSPRFTCGR HCWEVDVGTS TEWDLGVCRE SVHRKGRIQL
TTELGFWTVS LRDGGRLSAT TVPLTFLFVD RKLQRVGIFL DMGMQNVSFF DAESGSHVYT
FRSVSAEEPL RPFLAPSVPP NGDQGVLSIC PLMNSGTTDA PVRPGEAK*
mutated AA sequence MAALFQEASS CPVCSDYLEK PMSLECGCAV CLKCINSLQK EPHGEDLLCC CSSMVSRKNK
IRRNRQLERL ASHIKELEPK LKKILQMNPR MRKFQVDMTL DANTANNFLL ISDDLRSVRS
GRIRQNRQDL AERFDVSVCI LGSPRFTCGR HCWEVDVGTS TEWDLGVCRE SVHRKGRIQL
TTELGFWTVS LRDGGRLSAT TVPLTFLFVD RKLQRVGIFL DMGMQNVSFF DAESGSHVYT
FRSVSAEEPL RPFLAPSIPP NGDQGVLSIC PLMNSGTTDA PVRPGEAK*
speed 2.29 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