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MutationTaster - study a chromosomal position

MTQE documentation
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input seems to be ok - now mapping the variant to the different transcripts...
found 2 transcript(s)...
Querying Taster for transcript #1: ENST00000378842
Querying Taster for transcript #2: ENST00000450095
MT speed 0 s - this script 5.767076 s

Results


genesymbolpredictionprobabilitymodelprediction
problem
splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
GALTdisease_causing_automatic0.999864459331688simple_aaeaffected0R123Qsingle base exchangers111033675show file
GALTdisease_causing_automatic1without_aaeaffected0single base exchangers111033675show file

Taster files

Yum, tasty mutations...

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999864459331688 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM990635)
  • known disease mutation: rs25162 (pathogenic)
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr9:34647693G>AN/A show variant in all transcripts   IGV
HGNC symbol GALT
Ensembl transcript ID ENST00000378842
Genbank transcript ID NM_000155
UniProt peptide P07902
alteration type single base exchange
alteration region CDS
DNA changes c.368G>A
cDNA.410G>A
g.9564G>A
AA changes R123Q Score: 43 explain score(s)
position(s) of altered AA
if AA alteration in CDS
123
frameshift no
known variant Reference ID: rs111033675
Allele 'A' was neither found in ExAC nor 1000G.
known disease mutation: rs25162 (pathogenic for Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM990635)

known disease mutation at this position, please check HGMD for details (HGMD ID CM990635)
known disease mutation at this position, please check HGMD for details (HGMD ID CM990635)
regulatory features H2BK5me1, Histone, Histone 2B Lysine 5 mono-methylation
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me1, Histone, Histone 3 Lysine 4 Mono-Methylation
H3K4me2, Histone, Histone 3 Lysine 4 Di-Methylation
H3K4me3, Histone, Histone 3 Lysine 4 Tri-Methylation
H3K79me2, Histone, Histone 3 Lysine 79 di-methylation
H3K9ac, Histone, Histone 3 Lysine 9 Acetylation
H3K9me1, Histone, Histone 3 Lysine 9 mono-methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.8450.972
2.7610.999
(flanking)0.3870.999
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased9560wt: 0.59 / mu: 0.96wt: AGTCTGCTCGAGGAG
mu: AGTCTGCTCAAGGAG
 TCTG|ctcg
Donor marginally increased9555wt: 0.2260 / mu: 0.2335 (marginal change - not scored)wt: AGCAAAGTCTGCTCG
mu: AGCAAAGTCTGCTCA
 CAAA|gtct
Donor marginally increased9568wt: 0.7552 / mu: 0.8247 (marginal change - not scored)wt: CGAGGAGTCTGGTAA
mu: CAAGGAGTCTGGTAA
 AGGA|gtct
distance from splice site 10
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      123SDHPLFQAKSARGVCKVMCFHPWS
mutated  all conserved    123SAQGVCKVMCFHPW
Ptroglodytes  all identical  ENSPTRG00000020886  123SARGVCKVMCFHPW
Mmulatta  all identical  ENSMMUG00000020789  123AARGVCKVMCFHPW
Fcatus  all identical  ENSFCAG00000016304  123AARGVCKVMCFHPW
Mmusculus  all identical  ENSMUSG00000036073  104SDHPLFRAEAARGVCKVMCFHPW
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000016445  108DQHPLFQSKAARGVCKVMCFHPW
Drerio  all identical  ENSDARG00000069543  108DHHPLFQSKAARGVCKVMCFHPW
Dmelanogaster  all identical  FBgn0263200  102NDDPLFQIAPARGNCRVMCFHPK
Celegans  all conserved  ZK1058.3  103DENDDLFKQHEVKGVCKVICYHPN
Xtropicalis  not conserved  ENSXETG00000013206  98G---LYKSKCP-------CLYPW
protein features
start (aa)end (aa)featuredetails 
184184METALZinc (Potential).might get lost (downstream of altered splice site)
186186ACT_SITETele-UMP-histidine intermediate (By similarity).might get lost (downstream of altered splice site)
202202METALIron (Potential).might get lost (downstream of altered splice site)
258259CONFLICTRR -> VG (in Ref. 1; AAC83409).might get lost (downstream of altered splice site)
301301METALIron (Potential).might get lost (downstream of altered splice site)
319319METALIron (Potential).might get lost (downstream of altered splice site)
321321METALIron (Potential).might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1140 / 1140
position (AA) of stopcodon in wt / mu AA sequence 380 / 380
position of stopcodon in wt / mu cDNA 1182 / 1182
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 43 / 43
chromosome 9
strand 1
last intron/exon boundary 1102
theoretical NMD boundary in CDS 1009
length of CDS 1140
coding sequence (CDS) position 368
cDNA position
(for ins/del: last normal base / first normal base)
410
gDNA position
(for ins/del: last normal base / first normal base)
9564
chromosomal position
(for ins/del: last normal base / first normal base)
34647693
original gDNA sequence snippet TTTCCAAGCAAAGTCTGCTCGAGGAGTCTGGTAACTATGGA
altered gDNA sequence snippet TTTCCAAGCAAAGTCTGCTCAAGGAGTCTGGTAACTATGGA
original cDNA sequence snippet TTTCCAAGCAAAGTCTGCTCGAGGAGTCTGTAAGGTCATGT
altered cDNA sequence snippet TTTCCAAGCAAAGTCTGCTCAAGGAGTCTGTAAGGTCATGT
wildtype AA sequence MSRSGTDPQQ RQQASEADAA AATFRANDHQ HIRYNPLQDE WVLVSAHRMK RPWQGQVEPQ
LLKTVPRHDP LNPLCPGAIR ANGEVNPQYD STFLFDNDFP ALQPDAPSPG PSDHPLFQAK
SARGVCKVMC FHPWSDVTLP LMSVPEIRAV VDAWASVTEE LGAQYPWVQI FENKGAMMGC
SNPHPHCQVW ASSFLPDIAQ REERSQQAYK SQHGEPLLME YSRQELLRKE RLVLTSEHWL
VLVPFWATWP YQTLLLPRRH VRRLPELTPA ERDDLASIMK KLLTKYDNLF ETSFPYSMGW
HGAPTGSEAG ANWNHWQLHA HYYPPLLRSA TVRKFMVGYE MLAQAQRDLT PEQAAERLRA
LPEVHYHLGQ KDRETATIA*
mutated AA sequence MSRSGTDPQQ RQQASEADAA AATFRANDHQ HIRYNPLQDE WVLVSAHRMK RPWQGQVEPQ
LLKTVPRHDP LNPLCPGAIR ANGEVNPQYD STFLFDNDFP ALQPDAPSPG PSDHPLFQAK
SAQGVCKVMC FHPWSDVTLP LMSVPEIRAV VDAWASVTEE LGAQYPWVQI FENKGAMMGC
SNPHPHCQVW ASSFLPDIAQ REERSQQAYK SQHGEPLLME YSRQELLRKE RLVLTSEHWL
VLVPFWATWP YQTLLLPRRH VRRLPELTPA ERDDLASIMK KLLTKYDNLF ETSFPYSMGW
HGAPTGSEAG ANWNHWQLHA HYYPPLLRSA TVRKFMVGYE MLAQAQRDLT PEQAAERLRA
LPEVHYHLGQ KDRETATIA*
speed 1.67 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: without_aae, prob: 1 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • known disease mutation at this position (HGMD CM990635)
  • known disease mutation: rs25162 (pathogenic)
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr9:34647693G>AN/A show variant in all transcripts   IGV
HGNC symbol GALT
Ensembl transcript ID ENST00000450095
Genbank transcript ID NM_001258332
UniProt peptide P07902
alteration type single base exchange
alteration region intron
DNA changes g.9564G>A
AA changes N/A
position(s) of altered AA
if AA alteration in CDS
N/A
frameshift N/A
known variant Reference ID: rs111033675
Allele 'A' was neither found in ExAC nor 1000G.
known disease mutation: rs25162 (pathogenic for Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM990635)

known disease mutation at this position, please check HGMD for details (HGMD ID CM990635)
known disease mutation at this position, please check HGMD for details (HGMD ID CM990635)
regulatory features H2BK5me1, Histone, Histone 2B Lysine 5 mono-methylation
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me1, Histone, Histone 3 Lysine 4 Mono-Methylation
H3K4me2, Histone, Histone 3 Lysine 4 Di-Methylation
H3K4me3, Histone, Histone 3 Lysine 4 Tri-Methylation
H3K79me2, Histone, Histone 3 Lysine 79 di-methylation
H3K9ac, Histone, Histone 3 Lysine 9 Acetylation
H3K9me1, Histone, Histone 3 Lysine 9 mono-methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.8450.972
2.7610.999
(flanking)0.3870.999
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased9560wt: 0.59 / mu: 0.96wt: AGTCTGCTCGAGGAG
mu: AGTCTGCTCAAGGAG
 TCTG|ctcg
Donor marginally increased9555wt: 0.2260 / mu: 0.2335 (marginal change - not scored)wt: AGCAAAGTCTGCTCG
mu: AGCAAAGTCTGCTCA
 CAAA|gtct
Donor marginally increased9568wt: 0.7552 / mu: 0.8247 (marginal change - not scored)wt: CGAGGAGTCTGGTAA
mu: CAAGGAGTCTGGTAA
 AGGA|gtct
distance from splice site 136
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
N/A
protein features
start (aa)end (aa)featuredetails 
7575METALZinc (Potential).might get lost (downstream of altered splice site)
184184METALZinc (Potential).might get lost (downstream of altered splice site)
186186ACT_SITETele-UMP-histidine intermediate (By similarity).might get lost (downstream of altered splice site)
202202METALIron (Potential).might get lost (downstream of altered splice site)
258259CONFLICTRR -> VG (in Ref. 1; AAC83409).might get lost (downstream of altered splice site)
301301METALIron (Potential).might get lost (downstream of altered splice site)
319319METALIron (Potential).might get lost (downstream of altered splice site)
321321METALIron (Potential).might get lost (downstream of altered splice site)
length of protein N/A
AA sequence altered N/A
position of stopcodon in wt / mu CDS N/A
position (AA) of stopcodon in wt / mu AA sequence N/A
position of stopcodon in wt / mu cDNA N/A
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 9
strand 1
last intron/exon boundary 1004
theoretical NMD boundary in CDS 682
length of CDS 813
coding sequence (CDS) position N/A
cDNA position
(for ins/del: last normal base / first normal base)
N/A
gDNA position
(for ins/del: last normal base / first normal base)
9564
chromosomal position
(for ins/del: last normal base / first normal base)
34647693
original gDNA sequence snippet TTTCCAAGCAAAGTCTGCTCGAGGAGTCTGGTAACTATGGA
altered gDNA sequence snippet TTTCCAAGCAAAGTCTGCTCAAGGAGTCTGGTAACTATGGA
original cDNA sequence snippet N/A
altered cDNA sequence snippet N/A
wildtype AA sequence MTLSTLCVLG PSEPTESKVM CFHPWSDVTL PLMSVPEIRA VVDAWASVTE ELGAQYPWVQ
IFENKGAMMG CSNPHPHCQV WASSFLPDIA QREERSQQAY KSQHGEPLLM EYSRQELLRK
ERLVLTSEHW LVLVPFWATW PYQTLLLPRR HVRRLPELTP AERDDLASIM KKLLTKYDNL
FETSFPYSMG WHGAPTGSEA GANWNHWQLH AHYYPPLLRS ATVRKFMVGY EMLAQAQRDL
TPEQAAERLR ALPEVHYHLG QKDRETATIA *
mutated AA sequence N/A
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

Problems