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: ENST00000464300
Querying Taster for transcript #2: ENST00000483793
Querying Taster for transcript #3: ENST00000310366
Querying Taster for transcript #4: ENST00000493645
MT speed 0 s - this script 4.801859 s

Results

genesymbolpredictionprobabilitymodelprediction
problem		splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
PARP15polymorphism_automatic0.999999953627897simple_aaeaffectedG394Rsingle base exchangers12489170show file
PARP15polymorphism_automatic0.999999989761257simple_aaeaffectedG628Rsingle base exchangers12489170show file
PARP15polymorphism_automatic0.999999992391158simple_aaeaffectedG433Rsingle base exchangers12489170show file
PARP15polymorphism_automatic0.999999992391158simple_aaeaffectedG325Rsingle base exchangers12489170show file

Taster files

Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 4.63721031404863e-08 (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) chr3:122354792G>AN/A show variant in all transcripts   IGV
HGNC symbol PARP15
Ensembl transcript ID ENST00000310366
Genbank transcript ID NM_152615
UniProt peptide Q460N3
alteration type single base exchange
alteration region CDS
DNA changes c.1180G>A
cDNA.1275G>A
g.58344G>A
AA changes G394R Score: 125 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 394
frameshift no
known variant Reference ID: rs12489170
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC25331682919362
regulatory features DNase1, Open Chromatin, DNase1 Hypersensitive Site
Gene Associated, Regulatory Feature, Gene associated regulatory feature
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.770
5.0580.992
(flanking)5.0580.992
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased58341wt: 0.41 / mu: 0.52wt: TACTTACTGGAGTCTTCACAAAGGGACGTGCAGGATTAGTC
mu: TACTTACTGGAGTCTTCACAAAGAGACGTGCAGGATTAGTC		 acaa|AGGG
Donor increased58344wt: 0.79 / mu: 0.99wt: CAAAGGGACGTGCAG
mu: CAAAGAGACGTGCAG		 AAGG|gacg
Donor increased58337wt: 0.55 / mu: 0.67wt: GTCTTCACAAAGGGA
mu: GTCTTCACAAAGAGA		 CTTC|acaa
Donor increased58347wt: 0.52 / mu: 0.73wt: AGGGACGTGCAGGAT
mu: AGAGACGTGCAGGAT		 GGAC|gtgc
Donor marginally increased58342wt: 0.9988 / mu: 0.9990 (marginal change - not scored)wt: CACAAAGGGACGTGC
mu: CACAAAGAGACGTGC		 CAAA|ggga
Donor gained583390.85mu: CTTCACAAAGAGACG TCAC|aaag
distance from splice site 135
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      394VVRVLTGVFTKGRAGLVTPPPKNP
mutated  not conserved    394VVRVLTGVFTKRRAGLVTPPPKN
Ptroglodytes  all identical  ENSPTRG00000015296  628VVRVLTGVFTKGRAGLVTPPPKN
Mmulatta  all identical  ENSMMUG00000020547  572VVRVLTGVFTKGHAGLVTPPPKN
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  all identical  ENSGALG00000012072  1586LARVLVGQYSQGTQGAITPAAKN
Trubripes  all identical  ENSTRUG00000010891  349LAKVLVGDFTRGQAGLPAPPEK-
Drerio  all identical  ENSDARG00000074139  1759LAKVLVGDFTRGNSGLLVPPAKS
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000023399  1760LARVLTGTFTTGQTNMITPPPKN
protein features
start (aa)end (aa)featuredetails 
271442DOMAINMacro 2.lost
395412HELIXmight get lost (downstream of altered splice site)
420427STRANDmight get lost (downstream of altered splice site)
429439HELIXmight get lost (downstream of altered splice site)
460656DOMAINPARP catalytic.might get lost (downstream of altered splice site)
471476STRANDmight get lost (downstream of altered splice site)
482495HELIXmight get lost (downstream of altered splice site)
498508STRANDmight get lost (downstream of altered splice site)
509525HELIXmight get lost (downstream of altered splice site)
526528STRANDmight get lost (downstream of altered splice site)
532539STRANDmight get lost (downstream of altered splice site)
541543HELIXmight get lost (downstream of altered splice site)
544550HELIXmight get lost (downstream of altered splice site)
554556TURNmight get lost (downstream of altered splice site)
566573STRANDmight get lost (downstream of altered splice site)
574578HELIXmight get lost (downstream of altered splice site)
580582TURNmight get lost (downstream of altered splice site)
591599STRANDmight get lost (downstream of altered splice site)
602605STRANDmight get lost (downstream of altered splice site)
615617STRANDmight get lost (downstream of altered splice site)
620624STRANDmight get lost (downstream of altered splice site)
626630STRANDmight get lost (downstream of altered splice site)
632634STRANDmight get lost (downstream of altered splice site)
636640STRANDmight get lost (downstream of altered splice site)
645655STRANDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1335 / 1335
position (AA) of stopcodon in wt / mu AA sequence 445 / 445
position of stopcodon in wt / mu cDNA 1430 / 1430
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 96 / 96
chromosome 3
strand 1
last intron/exon boundary 1141
theoretical NMD boundary in CDS 995
length of CDS 1335
coding sequence (CDS) position 1180
cDNA position
(for ins/del: last normal base / first normal base)		 1275
gDNA position
(for ins/del: last normal base / first normal base)		 58344
chromosomal position
(for ins/del: last normal base / first normal base)		 122354792
original gDNA sequence snippet TTACTGGAGTCTTCACAAAGGGACGTGCAGGATTAGTCACC
altered gDNA sequence snippet TTACTGGAGTCTTCACAAAGAGACGTGCAGGATTAGTCACC
original cDNA sequence snippet TTACTGGAGTCTTCACAAAGGGACGTGCAGGATTAGTCACC
altered cDNA sequence snippet TTACTGGAGTCTTCACAAAGAGACGTGCAGGATTAGTCACC
wildtype AA sequence MLQRIGLIFL HNIVVVSNCF YFQAFLDEFT NWSRINPNKA RIPMAGDTQG VVGTVSKPCF
TAYEMKIGAI TFQVATGDIA TEQVDVIVNS TARTFNRKSG VSRAILEGAG QAVESECAVL
AAQPHRDFII TPGGCLKCKI IIHVPGGKDV RKTVTSVLEE CEQRKYTSVS LPAIGTGNAG
KNPITVADNI IDAIVDFSSQ HSTPSLKTVK VVIFQPELLN IFYDSMKKRD LSASLNFQST
FSMTTCNLPE HWTDMNHQLF CMVQLEPGQS EYNTIKDKFT RTCSSYAIEK IERIQNAFLW
QSYQVKKRQM DIKNDHKNNE RLLFHGTDAD SVPYVNQHGF NRSCAGKNAV SYGKGTYFAV
DASYSAKDTY SKPDSNGRKH MYVVRVLTGV FTKGRAGLVT PPPKNPHNPT DLFDSVTNNT
RSPKLFVVFF DNQAYPEYLI TFTA*
mutated AA sequence MLQRIGLIFL HNIVVVSNCF YFQAFLDEFT NWSRINPNKA RIPMAGDTQG VVGTVSKPCF
TAYEMKIGAI TFQVATGDIA TEQVDVIVNS TARTFNRKSG VSRAILEGAG QAVESECAVL
AAQPHRDFII TPGGCLKCKI IIHVPGGKDV RKTVTSVLEE CEQRKYTSVS LPAIGTGNAG
KNPITVADNI IDAIVDFSSQ HSTPSLKTVK VVIFQPELLN IFYDSMKKRD LSASLNFQST
FSMTTCNLPE HWTDMNHQLF CMVQLEPGQS EYNTIKDKFT RTCSSYAIEK IERIQNAFLW
QSYQVKKRQM DIKNDHKNNE RLLFHGTDAD SVPYVNQHGF NRSCAGKNAV SYGKGTYFAV
DASYSAKDTY SKPDSNGRKH MYVVRVLTGV FTKRRAGLVT PPPKNPHNPT DLFDSVTNNT
RSPKLFVVFF DNQAYPEYLI TFTA*
speed 0.45 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: 1.02387430987586e-08 (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) chr3:122354792G>AN/A show variant in all transcripts   IGV
HGNC symbol PARP15
Ensembl transcript ID ENST00000464300
Genbank transcript ID NM_001113523
UniProt peptide Q460N3
alteration type single base exchange
alteration region CDS
DNA changes c.1882G>A
cDNA.1948G>A
g.58344G>A
AA changes G628R Score: 125 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 628
frameshift no
known variant Reference ID: rs12489170
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC25331682919362
regulatory features DNase1, Open Chromatin, DNase1 Hypersensitive Site
Gene Associated, Regulatory Feature, Gene associated regulatory feature
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.770
5.0580.992
(flanking)5.0580.992
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased58341wt: 0.41 / mu: 0.52wt: TACTTACTGGAGTCTTCACAAAGGGACGTGCAGGATTAGTC
mu: TACTTACTGGAGTCTTCACAAAGAGACGTGCAGGATTAGTC		 acaa|AGGG
Donor increased58344wt: 0.79 / mu: 0.99wt: CAAAGGGACGTGCAG
mu: CAAAGAGACGTGCAG		 AAGG|gacg
Donor increased58337wt: 0.55 / mu: 0.67wt: GTCTTCACAAAGGGA
mu: GTCTTCACAAAGAGA		 CTTC|acaa
Donor increased58347wt: 0.52 / mu: 0.73wt: AGGGACGTGCAGGAT
mu: AGAGACGTGCAGGAT		 GGAC|gtgc
Donor marginally increased58342wt: 0.9988 / mu: 0.9990 (marginal change - not scored)wt: CACAAAGGGACGTGC
mu: CACAAAGAGACGTGC		 CAAA|ggga
Donor gained583390.85mu: CTTCACAAAGAGACG TCAC|aaag
distance from splice site 135
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      628VVRVLTGVFTKGRAGLVTPPPKNP
mutated  not conserved    628VVRVLTGVFTKRRAGLVTPPPKN
Ptroglodytes  all identical  ENSPTRG00000015296  628VVRVLTGVFTKGRAGLVTPPPKN
Mmulatta  all identical  ENSMMUG00000020547  572VVRVLTGVFTKGHAGLVTPPPKN
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  all identical  ENSGALG00000012072  1586LARVLVGQYSQGTQGAITPAAKN
Trubripes  all identical  ENSTRUG00000010891  349LAKVLVGDFTRGQAGLPAPPEK-
Drerio  all identical  ENSDARG00000074139  1760LAKVLVGDFTRGNSGLLVPPAKS
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000023399  1760LARVLTGTFTTGQTNMITPPPKN
protein features
start (aa)end (aa)featuredetails 
460656DOMAINPARP catalytic.lost
626630STRANDlost
632634STRANDmight get lost (downstream of altered splice site)
636640STRANDmight get lost (downstream of altered splice site)
645655STRANDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 2037 / 2037
position (AA) of stopcodon in wt / mu AA sequence 679 / 679
position of stopcodon in wt / mu cDNA 2103 / 2103
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 67 / 67
chromosome 3
strand 1
last intron/exon boundary 1814
theoretical NMD boundary in CDS 1697
length of CDS 2037
coding sequence (CDS) position 1882
cDNA position
(for ins/del: last normal base / first normal base)		 1948
gDNA position
(for ins/del: last normal base / first normal base)		 58344
chromosomal position
(for ins/del: last normal base / first normal base)		 122354792
original gDNA sequence snippet TTACTGGAGTCTTCACAAAGGGACGTGCAGGATTAGTCACC
altered gDNA sequence snippet TTACTGGAGTCTTCACAAAGAGACGTGCAGGATTAGTCACC
original cDNA sequence snippet TTACTGGAGTCTTCACAAAGGGACGTGCAGGATTAGTCACC
altered cDNA sequence snippet TTACTGGAGTCTTCACAAAGAGACGTGCAGGATTAGTCACC
wildtype AA sequence MAAPGPLPAA ALSPGAPTPR ELMHGVAGVT SRAGRDREAG SVLPAGNRGA RKASRRSSSR
SMSRDNKFSK KDCLSIRNVV ASIQTKEGLN LKLISGDVLY IWADVIVNSV PMNLQLGGGP
LSRAFLQKAG PMLQKELDDR RRETEEKVGN IFMTSGCNLD CKAVLHAVAP YWNNGAETSW
QIMANIIKKC LTTVEVLSFS SITFPMIGTG SLQFPKAVFA KLILSEVFEY SSSTRPITSP
LQEVHFLVYT NDDEGCQAFL DEFTNWSRIN PNKARIPMAG DTQGVVGTVS KPCFTAYEMK
IGAITFQVAT GDIATEQVDV IVNSTARTFN RKSGVSRAIL EGAGQAVESE CAVLAAQPHR
DFIITPGGCL KCKIIIHVPG GKDVRKTVTS VLEECEQRKY TSVSLPAIGT GNAGKNPITV
ADNIIDAIVD FSSQHSTPSL KTVKVVIFQP ELLNIFYDSM KKRDLSASLN FQSTFSMTTC
NLPEHWTDMN HQLFCMVQLE PGQSEYNTIK DKFTRTCSSY AIEKIERIQN AFLWQSYQVK
KRQMDIKNDH KNNERLLFHG TDADSVPYVN QHGFNRSCAG KNAVSYGKGT YFAVDASYSA
KDTYSKPDSN GRKHMYVVRV LTGVFTKGRA GLVTPPPKNP HNPTDLFDSV TNNTRSPKLF
VVFFDNQAYP EYLITFTA*
mutated AA sequence MAAPGPLPAA ALSPGAPTPR ELMHGVAGVT SRAGRDREAG SVLPAGNRGA RKASRRSSSR
SMSRDNKFSK KDCLSIRNVV ASIQTKEGLN LKLISGDVLY IWADVIVNSV PMNLQLGGGP
LSRAFLQKAG PMLQKELDDR RRETEEKVGN IFMTSGCNLD CKAVLHAVAP YWNNGAETSW
QIMANIIKKC LTTVEVLSFS SITFPMIGTG SLQFPKAVFA KLILSEVFEY SSSTRPITSP
LQEVHFLVYT NDDEGCQAFL DEFTNWSRIN PNKARIPMAG DTQGVVGTVS KPCFTAYEMK
IGAITFQVAT GDIATEQVDV IVNSTARTFN RKSGVSRAIL EGAGQAVESE CAVLAAQPHR
DFIITPGGCL KCKIIIHVPG GKDVRKTVTS VLEECEQRKY TSVSLPAIGT GNAGKNPITV
ADNIIDAIVD FSSQHSTPSL KTVKVVIFQP ELLNIFYDSM KKRDLSASLN FQSTFSMTTC
NLPEHWTDMN HQLFCMVQLE PGQSEYNTIK DKFTRTCSSY AIEKIERIQN AFLWQSYQVK
KRQMDIKNDH KNNERLLFHG TDADSVPYVN QHGFNRSCAG KNAVSYGKGT YFAVDASYSA
KDTYSKPDSN GRKHMYVVRV LTGVFTKRRA GLVTPPPKNP HNPTDLFDSV TNNTRSPKLF
VVFFDNQAYP EYLITFTA*
speed 0.48 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: 7.60884218502144e-09 (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) chr3:122354792G>AN/A show variant in all transcripts   IGV
HGNC symbol PARP15
Ensembl transcript ID ENST00000483793
Genbank transcript ID N/A
UniProt peptide Q460N3
alteration type single base exchange
alteration region CDS
DNA changes c.1297G>A
cDNA.1337G>A
g.58344G>A
AA changes G433R Score: 125 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 433
frameshift no
known variant Reference ID: rs12489170
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC25331682919362
regulatory features DNase1, Open Chromatin, DNase1 Hypersensitive Site
Gene Associated, Regulatory Feature, Gene associated regulatory feature
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.770
5.0580.992
(flanking)5.0580.992
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased58341wt: 0.41 / mu: 0.52wt: TACTTACTGGAGTCTTCACAAAGGGACGTGCAGGATTAGTC
mu: TACTTACTGGAGTCTTCACAAAGAGACGTGCAGGATTAGTC		 acaa|AGGG
Donor increased58344wt: 0.79 / mu: 0.99wt: CAAAGGGACGTGCAG
mu: CAAAGAGACGTGCAG		 AAGG|gacg
Donor increased58337wt: 0.55 / mu: 0.67wt: GTCTTCACAAAGGGA
mu: GTCTTCACAAAGAGA		 CTTC|acaa
Donor increased58347wt: 0.52 / mu: 0.73wt: AGGGACGTGCAGGAT
mu: AGAGACGTGCAGGAT		 GGAC|gtgc
Donor marginally increased58342wt: 0.9988 / mu: 0.9990 (marginal change - not scored)wt: CACAAAGGGACGTGC
mu: CACAAAGAGACGTGC		 CAAA|ggga
Donor gained583390.85mu: CTTCACAAAGAGACG TCAC|aaag
distance from splice site 135
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      433VVRVLTGVFTKGRAGLVTPPPKNP
mutated  not conserved    433VVRVLTGVFTKRRAGLVTPPPKN
Ptroglodytes  all identical  ENSPTRG00000015296  628VVRVLTGVFTKGRAGL
Mmulatta  all identical  ENSMMUG00000020547  572VVRVLTGVFTKGHAG
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  all identical  ENSGALG00000012072  1586LARVLVGQYSQGTQGAITPAAKN
Trubripes  all identical  ENSTRUG00000010891  349LAKVLVGDFTRGQAGLPAPPEK-
Drerio  all identical  ENSDARG00000074139  1760LAKVLVGDFTRGNSGLLVPPAKS
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000023399  1760LARVLTGTFTTGQTNMITPPPKN
protein features
start (aa)end (aa)featuredetails 
271442DOMAINMacro 2.lost
429439HELIXlost
460656DOMAINPARP catalytic.might get lost (downstream of altered splice site)
471476STRANDmight get lost (downstream of altered splice site)
482495HELIXmight get lost (downstream of altered splice site)
498508STRANDmight get lost (downstream of altered splice site)
509525HELIXmight get lost (downstream of altered splice site)
526528STRANDmight get lost (downstream of altered splice site)
532539STRANDmight get lost (downstream of altered splice site)
541543HELIXmight get lost (downstream of altered splice site)
544550HELIXmight get lost (downstream of altered splice site)
554556TURNmight get lost (downstream of altered splice site)
566573STRANDmight get lost (downstream of altered splice site)
574578HELIXmight get lost (downstream of altered splice site)
580582TURNmight get lost (downstream of altered splice site)
591599STRANDmight get lost (downstream of altered splice site)
602605STRANDmight get lost (downstream of altered splice site)
615617STRANDmight get lost (downstream of altered splice site)
620624STRANDmight get lost (downstream of altered splice site)
626630STRANDmight get lost (downstream of altered splice site)
632634STRANDmight get lost (downstream of altered splice site)
636640STRANDmight get lost (downstream of altered splice site)
645655STRANDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1452 / 1452
position (AA) of stopcodon in wt / mu AA sequence 484 / 484
position of stopcodon in wt / mu cDNA 1492 / 1492
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 41 / 41
chromosome 3
strand 1
last intron/exon boundary 1203
theoretical NMD boundary in CDS 1112
length of CDS 1452
coding sequence (CDS) position 1297
cDNA position
(for ins/del: last normal base / first normal base)		 1337
gDNA position
(for ins/del: last normal base / first normal base)		 58344
chromosomal position
(for ins/del: last normal base / first normal base)		 122354792
original gDNA sequence snippet TTACTGGAGTCTTCACAAAGGGACGTGCAGGATTAGTCACC
altered gDNA sequence snippet TTACTGGAGTCTTCACAAAGAGACGTGCAGGATTAGTCACC
original cDNA sequence snippet TTACTGGAGTCTTCACAAAGGGACGTGCAGGATTAGTCACC
altered cDNA sequence snippet TTACTGGAGTCTTCACAAAGAGACGTGCAGGATTAGTCACC
wildtype AA sequence MAAPGPLPAA ALSPGAPTPR ELMHGVAGVT SRAGRDREAG SVLPAGNRGA RKASRRSSSR
SMSRDNKFSK KDCLSIRNVV ASIQTKEGLN LKLISGDVLY IWADVIVNSV PMNLQLGGGP
LSRAFLQKAG PMLQKELDDR RRETEEKVGN IFMTSGCNLD CKAVLHAVAP YWNNGAETSW
QVATGDIATE QVDVIVNSTA RTFNRKSGVS RAILEGAGQA VESECAVLAA QPHRDFIITP
GGCLKCKIII HVPGGKDVRK TVTSVLEECE QRKYTSVSLP AIGTGNLPEH WTDMNHQLFC
MVQLEPGQSE YNTIKDKFTR TCSSYAIEKI ERIQNAFLWQ SYQVKKRQMD IKNDHKNNER
LLFHGTDADS VPYVNQHGFN RSCAGKNAVS YGKGTYFAVD ASYSAKDTYS KPDSNGRKHM
YVVRVLTGVF TKGRAGLVTP PPKNPHNPTD LFDSVTNNTR SPKLFVVFFD NQAYPEYLIT
FTA*
mutated AA sequence MAAPGPLPAA ALSPGAPTPR ELMHGVAGVT SRAGRDREAG SVLPAGNRGA RKASRRSSSR
SMSRDNKFSK KDCLSIRNVV ASIQTKEGLN LKLISGDVLY IWADVIVNSV PMNLQLGGGP
LSRAFLQKAG PMLQKELDDR RRETEEKVGN IFMTSGCNLD CKAVLHAVAP YWNNGAETSW
QVATGDIATE QVDVIVNSTA RTFNRKSGVS RAILEGAGQA VESECAVLAA QPHRDFIITP
GGCLKCKIII HVPGGKDVRK TVTSVLEECE QRKYTSVSLP AIGTGNLPEH WTDMNHQLFC
MVQLEPGQSE YNTIKDKFTR TCSSYAIEKI ERIQNAFLWQ SYQVKKRQMD IKNDHKNNER
LLFHGTDADS VPYVNQHGFN RSCAGKNAVS YGKGTYFAVD ASYSAKDTYS KPDSNGRKHM
YVVRVLTGVF TKRRAGLVTP PPKNPHNPTD LFDSVTNNTR SPKLFVVFFD NQAYPEYLIT
FTA*
speed 1.18 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: 7.60884218502144e-09 (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) chr3:122354792G>AN/A show variant in all transcripts   IGV
HGNC symbol PARP15
Ensembl transcript ID ENST00000493645
Genbank transcript ID N/A
UniProt peptide Q460N3
alteration type single base exchange
alteration region CDS
DNA changes c.973G>A
cDNA.1068G>A
g.58344G>A
AA changes G325R Score: 125 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 325
frameshift no
known variant Reference ID: rs12489170
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC25331682919362
regulatory features DNase1, Open Chromatin, DNase1 Hypersensitive Site
Gene Associated, Regulatory Feature, Gene associated regulatory feature
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-1.770
5.0580.992
(flanking)5.0580.992
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased58341wt: 0.41 / mu: 0.52wt: TACTTACTGGAGTCTTCACAAAGGGACGTGCAGGATTAGTC
mu: TACTTACTGGAGTCTTCACAAAGAGACGTGCAGGATTAGTC		 acaa|AGGG
Donor increased58344wt: 0.79 / mu: 0.99wt: CAAAGGGACGTGCAG
mu: CAAAGAGACGTGCAG		 AAGG|gacg
Donor increased58337wt: 0.55 / mu: 0.67wt: GTCTTCACAAAGGGA
mu: GTCTTCACAAAGAGA		 CTTC|acaa
Donor increased58347wt: 0.52 / mu: 0.73wt: AGGGACGTGCAGGAT
mu: AGAGACGTGCAGGAT		 GGAC|gtgc
Donor marginally increased58342wt: 0.9988 / mu: 0.9990 (marginal change - not scored)wt: CACAAAGGGACGTGC
mu: CACAAAGAGACGTGC		 CAAA|ggga
Donor gained583390.85mu: CTTCACAAAGAGACG TCAC|aaag
distance from splice site 135
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      325VVRVLTGVFTKGRAGLVTPPPKNP
mutated  not conserved    325VVRVLTGVFTKRRAGLVTPPPKN
Ptroglodytes  all identical  ENSPTRG00000015296  628VVRVLTGVFTKGRAGLVTPPPKN
Mmulatta  all identical  ENSMMUG00000020547  572VVRVLTGVFTKGHAGLVTPPPKN
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  all identical  ENSGALG00000012072  1586LARVLVGQYSQGTQGAITPAAKN
Trubripes  all identical  ENSTRUG00000010891  349LAKVLVGDFTRGQAGLPAPPEK-
Drerio  all identical  ENSDARG00000074139  1760LAKVLVGDFTRGNSGLLVPPAKS
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000023399  1760LARVLTGTFTTGQTNMITPPPKN
protein features
start (aa)end (aa)featuredetails 
271442DOMAINMacro 2.lost
323333HELIXlost
339344STRANDmight get lost (downstream of altered splice site)
348357STRANDmight get lost (downstream of altered splice site)
362375HELIXmight get lost (downstream of altered splice site)
380383STRANDmight get lost (downstream of altered splice site)
395412HELIXmight get lost (downstream of altered splice site)
420427STRANDmight get lost (downstream of altered splice site)
429439HELIXmight get lost (downstream of altered splice site)
460656DOMAINPARP catalytic.might get lost (downstream of altered splice site)
471476STRANDmight get lost (downstream of altered splice site)
482495HELIXmight get lost (downstream of altered splice site)
498508STRANDmight get lost (downstream of altered splice site)
509525HELIXmight get lost (downstream of altered splice site)
526528STRANDmight get lost (downstream of altered splice site)
532539STRANDmight get lost (downstream of altered splice site)
541543HELIXmight get lost (downstream of altered splice site)
544550HELIXmight get lost (downstream of altered splice site)
554556TURNmight get lost (downstream of altered splice site)
566573STRANDmight get lost (downstream of altered splice site)
574578HELIXmight get lost (downstream of altered splice site)
580582TURNmight get lost (downstream of altered splice site)
591599STRANDmight get lost (downstream of altered splice site)
602605STRANDmight get lost (downstream of altered splice site)
615617STRANDmight get lost (downstream of altered splice site)
620624STRANDmight get lost (downstream of altered splice site)
626630STRANDmight get lost (downstream of altered splice site)
632634STRANDmight get lost (downstream of altered splice site)
636640STRANDmight get lost (downstream of altered splice site)
645655STRANDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1128 / 1128
position (AA) of stopcodon in wt / mu AA sequence 376 / 376
position of stopcodon in wt / mu cDNA 1223 / 1223
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 96 / 96
chromosome 3
strand 1
last intron/exon boundary 934
theoretical NMD boundary in CDS 788
length of CDS 1128
coding sequence (CDS) position 973
cDNA position
(for ins/del: last normal base / first normal base)		 1068
gDNA position
(for ins/del: last normal base / first normal base)		 58344
chromosomal position
(for ins/del: last normal base / first normal base)		 122354792
original gDNA sequence snippet TTACTGGAGTCTTCACAAAGGGACGTGCAGGATTAGTCACC
altered gDNA sequence snippet TTACTGGAGTCTTCACAAAGAGACGTGCAGGATTAGTCACC
original cDNA sequence snippet TTACTGGAGTCTTCACAAAGGGACGTGCAGGATTAGTCACC
altered cDNA sequence snippet TTACTGGAGTCTTCACAAAGAGACGTGCAGGATTAGTCACC
wildtype AA sequence MLQRIGLIFL HNIVVVSNCF YFQAFLDEFT NWSRINPNKA RIPMAGDTQG VVGTVSKPCF
TAYEMKIGAI TFQVATGDIA TEQVDVIVNS TARTFNRKSG VSRAILEGAG QAVESECAVL
AAQPHRDFII TPGGCLKCKI IIHVPGGKDV RKTVTSVLEE CEQRKYTSVS LPAIGTGNLP
EHWTDMNHQL FCMVQLEPGQ SEYNTIKDKF TRTCSSYAIE KIERIQNAFL WQSYQVKKRQ
MDIKNDHKNN ERLLFHGTDA DSVPYVNQHG FNRSCAGKNA VSYGKGTYFA VDASYSAKDT
YSKPDSNGRK HMYVVRVLTG VFTKGRAGLV TPPPKNPHNP TDLFDSVTNN TRSPKLFVVF
FDNQAYPEYL ITFTA*
mutated AA sequence MLQRIGLIFL HNIVVVSNCF YFQAFLDEFT NWSRINPNKA RIPMAGDTQG VVGTVSKPCF
TAYEMKIGAI TFQVATGDIA TEQVDVIVNS TARTFNRKSG VSRAILEGAG QAVESECAVL
AAQPHRDFII TPGGCLKCKI IIHVPGGKDV RKTVTSVLEE CEQRKYTSVS LPAIGTGNLP
EHWTDMNHQL FCMVQLEPGQ SEYNTIKDKF TRTCSSYAIE KIERIQNAFL WQSYQVKKRQ
MDIKNDHKNN ERLLFHGTDA DSVPYVNQHG FNRSCAGKNA VSYGKGTYFA VDASYSAKDT
YSKPDSNGRK HMYVVRVLTG VFTKRRAGLV TPPPKNPHNP TDLFDSVTNN TRSPKLFVVF
FDNQAYPEYL ITFTA*
speed 1.16 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