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 2 transcript(s)...
Querying Taster for transcript #1: ENST00000382848
Querying Taster for transcript #2: ENST00000382844
MT speed 0 s - this script 3.420043 s

Results

genesymbolpredictionprobabilitymodelprediction
problem		splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
GJB2disease_causing_automatic0.999999999769526simple_aaeaffected0G45Esingle base exchangers72561723show file
GJB2disease_causing_automatic0.999999999769526simple_aaeaffected0G45Esingle base exchangers72561723show file

Taster files

Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999769526 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM990689)
  • known disease mutation: rs17033 (pathogenic)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr13:20763587C>TN/A show variant in all transcripts   IGV
HGNC symbol GJB2
Ensembl transcript ID ENST00000382848
Genbank transcript ID NM_004004
UniProt peptide P29033
alteration type single base exchange
alteration region CDS
DNA changes c.134G>A
cDNA.272G>A
g.3451G>A
AA changes G45E Score: 98 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 45
frameshift no
known variant Reference ID: rs72561723
Allele 'T' was neither found in ExAC nor 1000G.
known disease mutation: rs17033 (pathogenic for Keratitis-ichthyosis-deafness syndrome, autosomal dominant|Deafness, autosomal recessive 1A) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM990689)

known disease mutation at this position, please check HGMD for details (HGMD ID CM990689)
known disease mutation at this position, please check HGMD for details (HGMD ID CM990689)
regulatory features Promoter Associated, Regulatory Feature, Promoter like regulatory feature
Max, Transcription Factor, Max TF binding
Gabp, Transcription Factor, Gabp TF binding
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
Gene Associated, Regulatory Feature, Gene associated regulatory feature
CTCF, Transcription Factor, CCCTC-binding factor
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.460.925
6.0281
(flanking)6.0281
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased3447wt: 0.24 / mu: 0.97wt: AGGTGTGGGGAGATG
mu: AGGTGTGGGAAGATG		 GTGT|gggg
Donor increased3455wt: 0.34 / mu: 0.57wt: GGAGATGAGCAGGCC
mu: GAAGATGAGCAGGCC		 AGAT|gagc
Donor marginally increased3452wt: 0.9788 / mu: 0.9895 (marginal change - not scored)wt: TGGGGAGATGAGCAG
mu: TGGGAAGATGAGCAG		 GGGA|gatg
distance from splice site 156
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      45MILVVAAKEVWGDEQADFVCNTLQ
mutated  not conserved    45MILVVAAKEVWEDEQADFVCNTL
Ptroglodytes  all identical  ENSPTRG00000031248  45MILVVAAKEVWGDEQADFVCNTL
Mmulatta  all identical  ENSMMUG00000010522  45MILVVAAKEVWGDEQADFVCNTL
Fcatus  all identical  ENSFCAG00000006961  45MILVVAAKEVWGDEQADFVCNTL
Mmusculus  all identical  ENSMUSG00000046352  45MILVVAAKEVWGDEQADFVCNTL
Ggallus  all identical  ENSGALG00000017136  45MILVVAAERVWGDEQDDFICNTL
Trubripes  no homologue    
Drerio  all identical  ENSDARG00000042707  45CILVIAAETVWGDEQSDFTCNTQ
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000026112  45MILVVAAESVWGDEQSDFTCNTL
protein features
start (aa)end (aa)featuredetails 
4175TOPO_DOMExtracellular (Potential).lost
4649HELIXmight get lost (downstream of altered splice site)
5254STRANDmight get lost (downstream of altered splice site)
5353DISULFIDmight get lost (downstream of altered splice site)
6060DISULFIDmight get lost (downstream of altered splice site)
6066HELIXmight get lost (downstream of altered splice site)
6464DISULFIDmight get lost (downstream of altered splice site)
7383HELIXmight get lost (downstream of altered splice site)
7698TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
85105HELIXmight get lost (downstream of altered splice site)
8686CONFLICTT -> S (in Ref. 1; AAD21314).might get lost (downstream of altered splice site)
99131TOPO_DOMCytoplasmic (Potential).might get lost (downstream of altered splice site)
106108TURNmight get lost (downstream of altered splice site)
112112CONFLICTK -> N (in Ref. 4; AAY25170).might get lost (downstream of altered splice site)
126130TURNmight get lost (downstream of altered splice site)
131156HELIXmight get lost (downstream of altered splice site)
132154TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
155192TOPO_DOMExtracellular (Potential).might get lost (downstream of altered splice site)
157159TURNmight get lost (downstream of altered splice site)
160162STRANDmight get lost (downstream of altered splice site)
165169STRANDmight get lost (downstream of altered splice site)
169169DISULFIDmight get lost (downstream of altered splice site)
174174DISULFIDmight get lost (downstream of altered splice site)
174181STRANDmight get lost (downstream of altered splice site)
180180DISULFIDmight get lost (downstream of altered splice site)
185215HELIXmight get lost (downstream of altered splice site)
193215TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
216226TOPO_DOMCytoplasmic (Potential).might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 681 / 681
position (AA) of stopcodon in wt / mu AA sequence 227 / 227
position of stopcodon in wt / mu cDNA 819 / 819
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 139 / 139
chromosome 13
strand -1
last intron/exon boundary 117
theoretical NMD boundary in CDS cannot be calculated, too little distance between start ATG and last intron/exon boundary
length of CDS 681
coding sequence (CDS) position 134
cDNA position
(for ins/del: last normal base / first normal base)		 272
gDNA position
(for ins/del: last normal base / first normal base)		 3451
chromosomal position
(for ins/del: last normal base / first normal base)		 20763587
original gDNA sequence snippet GGCTGCAAAGGAGGTGTGGGGAGATGAGCAGGCCGACTTTG
altered gDNA sequence snippet GGCTGCAAAGGAGGTGTGGGAAGATGAGCAGGCCGACTTTG
original cDNA sequence snippet GGCTGCAAAGGAGGTGTGGGGAGATGAGCAGGCCGACTTTG
altered cDNA sequence snippet GGCTGCAAAGGAGGTGTGGGAAGATGAGCAGGCCGACTTTG
wildtype AA sequence MDWGTLQTIL GGVNKHSTSI GKIWLTVLFI FRIMILVVAA KEVWGDEQAD FVCNTLQPGC
KNVCYDHYFP ISHIRLWALQ LIFVSTPALL VAMHVAYRRH EKKRKFIKGE IKSEFKDIEE
IKTQKVRIEG SLWWTYTSSI FFRVIFEAAF MYVFYVMYDG FSMQRLVKCN AWPCPNTVDC
FVSRPTEKTV FTVFMIAVSG ICILLNVTEL CYLLIRYCSG KSKKPV*
mutated AA sequence MDWGTLQTIL GGVNKHSTSI GKIWLTVLFI FRIMILVVAA KEVWEDEQAD FVCNTLQPGC
KNVCYDHYFP ISHIRLWALQ LIFVSTPALL VAMHVAYRRH EKKRKFIKGE IKSEFKDIEE
IKTQKVRIEG SLWWTYTSSI FFRVIFEAAF MYVFYVMYDG FSMQRLVKCN AWPCPNTVDC
FVSRPTEKTV FTVFMIAVSG ICILLNVTEL CYLLIRYCSG KSKKPV*
speed 0.76 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

disease causing

 Model: simple_aae, prob: 0.999999999769526 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM990689)
  • known disease mutation: rs17033 (pathogenic)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr13:20763587C>TN/A show variant in all transcripts   IGV
HGNC symbol GJB2
Ensembl transcript ID ENST00000382844
Genbank transcript ID N/A
UniProt peptide P29033
alteration type single base exchange
alteration region CDS
DNA changes c.134G>A
cDNA.333G>A
g.3451G>A
AA changes G45E Score: 98 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 45
frameshift no
known variant Reference ID: rs72561723
Allele 'T' was neither found in ExAC nor 1000G.
known disease mutation: rs17033 (pathogenic for Keratitis-ichthyosis-deafness syndrome, autosomal dominant|Deafness, autosomal recessive 1A) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM990689)

known disease mutation at this position, please check HGMD for details (HGMD ID CM990689)
known disease mutation at this position, please check HGMD for details (HGMD ID CM990689)
regulatory features Promoter Associated, Regulatory Feature, Promoter like regulatory feature
Max, Transcription Factor, Max TF binding
Gabp, Transcription Factor, Gabp TF binding
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
Gene Associated, Regulatory Feature, Gene associated regulatory feature
CTCF, Transcription Factor, CCCTC-binding factor
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.460.925
6.0281
(flanking)6.0281
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased3447wt: 0.24 / mu: 0.97wt: AGGTGTGGGGAGATG
mu: AGGTGTGGGAAGATG		 GTGT|gggg
Donor increased3455wt: 0.34 / mu: 0.57wt: GGAGATGAGCAGGCC
mu: GAAGATGAGCAGGCC		 AGAT|gagc
Donor marginally increased3452wt: 0.9788 / mu: 0.9895 (marginal change - not scored)wt: TGGGGAGATGAGCAG
mu: TGGGAAGATGAGCAG		 GGGA|gatg
distance from splice site 333
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      45MILVVAAKEVWGDEQADFVCNTLQ
mutated  not conserved    45MILVVAAKEVWEDEQADFVCNTL
Ptroglodytes  all identical  ENSPTRG00000031248  45MILVVAAKEVWGDEQADFVCNTL
Mmulatta  all identical  ENSMMUG00000010522  45MILVVAAKEVWGDEQADFVCNTL
Fcatus  all identical  ENSFCAG00000006961  45MILVVAAKEVWGDEQADFVCNTL
Mmusculus  all identical  ENSMUSG00000046352  45MILVVAAKEVWGDEQADFVCNTL
Ggallus  all identical  ENSGALG00000017136  45MILVVAAERVWGDEQDDFICNTL
Trubripes  no homologue    
Drerio  all identical  ENSDARG00000042707  45CILVIAAETVWGDEQSDFTCNTQ
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000026112  45MILVVAAESVWGDEQSDFTCNTL
protein features
start (aa)end (aa)featuredetails 
4175TOPO_DOMExtracellular (Potential).lost
4649HELIXmight get lost (downstream of altered splice site)
5254STRANDmight get lost (downstream of altered splice site)
5353DISULFIDmight get lost (downstream of altered splice site)
6060DISULFIDmight get lost (downstream of altered splice site)
6066HELIXmight get lost (downstream of altered splice site)
6464DISULFIDmight get lost (downstream of altered splice site)
7383HELIXmight get lost (downstream of altered splice site)
7698TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
85105HELIXmight get lost (downstream of altered splice site)
8686CONFLICTT -> S (in Ref. 1; AAD21314).might get lost (downstream of altered splice site)
99131TOPO_DOMCytoplasmic (Potential).might get lost (downstream of altered splice site)
106108TURNmight get lost (downstream of altered splice site)
112112CONFLICTK -> N (in Ref. 4; AAY25170).might get lost (downstream of altered splice site)
126130TURNmight get lost (downstream of altered splice site)
131156HELIXmight get lost (downstream of altered splice site)
132154TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
155192TOPO_DOMExtracellular (Potential).might get lost (downstream of altered splice site)
157159TURNmight get lost (downstream of altered splice site)
160162STRANDmight get lost (downstream of altered splice site)
165169STRANDmight get lost (downstream of altered splice site)
169169DISULFIDmight get lost (downstream of altered splice site)
174174DISULFIDmight get lost (downstream of altered splice site)
174181STRANDmight get lost (downstream of altered splice site)
180180DISULFIDmight get lost (downstream of altered splice site)
185215HELIXmight get lost (downstream of altered splice site)
193215TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
216226TOPO_DOMCytoplasmic (Potential).might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 681 / 681
position (AA) of stopcodon in wt / mu AA sequence 227 / 227
position of stopcodon in wt / mu cDNA 880 / 880
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 200 / 200
chromosome 13
strand -1
last intron/exon boundary 1
theoretical NMD boundary in CDS cannot be calculated, too little distance between start ATG and last intron/exon boundary
length of CDS 681
coding sequence (CDS) position 134
cDNA position
(for ins/del: last normal base / first normal base)		 333
gDNA position
(for ins/del: last normal base / first normal base)		 3451
chromosomal position
(for ins/del: last normal base / first normal base)		 20763587
original gDNA sequence snippet GGCTGCAAAGGAGGTGTGGGGAGATGAGCAGGCCGACTTTG
altered gDNA sequence snippet GGCTGCAAAGGAGGTGTGGGAAGATGAGCAGGCCGACTTTG
original cDNA sequence snippet GGCTGCAAAGGAGGTGTGGGGAGATGAGCAGGCCGACTTTG
altered cDNA sequence snippet GGCTGCAAAGGAGGTGTGGGAAGATGAGCAGGCCGACTTTG
wildtype AA sequence MDWGTLQTIL GGVNKHSTSI GKIWLTVLFI FRIMILVVAA KEVWGDEQAD FVCNTLQPGC
KNVCYDHYFP ISHIRLWALQ LIFVSTPALL VAMHVAYRRH EKKRKFIKGE IKSEFKDIEE
IKTQKVRIEG SLWWTYTSSI FFRVIFEAAF MYVFYVMYDG FSMQRLVKCN AWPCPNTVDC
FVSRPTEKTV FTVFMIAVSG ICILLNVTEL CYLLIRYCSG KSKKPV*
mutated AA sequence MDWGTLQTIL GGVNKHSTSI GKIWLTVLFI FRIMILVVAA KEVWEDEQAD FVCNTLQPGC
KNVCYDHYFP ISHIRLWALQ LIFVSTPALL VAMHVAYRRH EKKRKFIKGE IKSEFKDIEE
IKTQKVRIEG SLWWTYTSSI FFRVIFEAAF MYVFYVMYDG FSMQRLVKCN AWPCPNTVDC
FVSRPTEKTV FTVFMIAVSG ICILLNVTEL CYLLIRYCSG KSKKPV*
speed 0.62 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

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