Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.000981503218154572 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM990663)
  • known disease mutation: rs25263 (pathogenic)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr9:34648856G>CN/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.785G>C
cDNA.827G>C
g.10727G>C
AA changes R262P Score: 103 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 262
frameshift no
known variant Reference ID: rs111033763
Allele 'C' was neither found in ExAC nor 1000G.
known disease mutation: rs25263 (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 CM990663)

known disease mutation at this position, please check HGMD for details (HGMD ID CM990663)
known disease mutation at this position, please check HGMD for details (HGMD ID CM990663)
regulatory features H2BK5me1, Histone, Histone 2B Lysine 5 mono-methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me1, Histone, Histone 3 Lysine 4 Mono-Methylation
H3K9me1, Histone, Histone 3 Lysine 9 mono-methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)1.3390.845
-0.3710.209
(flanking)0.230.222
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased10724wt: 0.36 / mu: 0.47wt: GCTGCTGCCCCGTCGGCATGTGCGGCGGCTACCTGAGCTGA
mu: GCTGCTGCCCCGTCGGCATGTGCCGCGGCTACCTGAGCTGA		 atgt|GCGG
Acc marginally increased10718wt: 0.8431 / mu: 0.8522 (marginal change - not scored)wt: GACACTGCTGCTGCCCCGTCGGCATGTGCGGCGGCTACCTG
mu: GACACTGCTGCTGCCCCGTCGGCATGTGCCGCGGCTACCTG		 gtcg|GCAT
distance from splice site 36
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      262YQTLLLPRRHVRRLPELTPAERDD
mutated  not conserved    262YQTLLLPRRHVPRLPELTPAERD
Ptroglodytes  all identical  ENSPTRG00000020886  262YQTLLLPRRHVRRLPELTPAERD
Mmulatta  all conserved  ENSMMUG00000020789  262YQTLLLPRRHVQRLPELTPAERD
Fcatus  all identical  ENSFCAG00000016304  262FQTLLLPRRHVRRLPELTPAERD
Mmusculus  all identical  ENSMUSG00000036073  243VRRLPELNPAERD
Ggallus  no homologue    
Trubripes  not conserved  ENSTRUG00000016445  247YQTLLLPRRHILRITELTAEERK
Drerio  not conserved  ENSDARG00000069543  247FQTLLLPRRHVLRLPDLTTQERD
Dmelanogaster  all conserved  FBgn0263200  241FETMLISRNNNKRINDLTAEQRY
Celegans  not conserved  ZK1058.3  243YETMLLPNRHVERFTD
Xtropicalis  all identical  ENSXETG00000013206  226TSSLRRQLR-LQDLSQRRAP
protein features
start (aa)end (aa)featuredetails 
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 785
cDNA position
(for ins/del: last normal base / first normal base)		 827
gDNA position
(for ins/del: last normal base / first normal base)		 10727
chromosomal position
(for ins/del: last normal base / first normal base)		 34648856
original gDNA sequence snippet GCTGCCCCGTCGGCATGTGCGGCGGCTACCTGAGCTGACCC
altered gDNA sequence snippet GCTGCCCCGTCGGCATGTGCCGCGGCTACCTGAGCTGACCC
original cDNA sequence snippet GCTGCCCCGTCGGCATGTGCGGCGGCTACCTGAGCTGACCC
altered cDNA sequence snippet GCTGCCCCGTCGGCATGTGCCGCGGCTACCTGAGCTGACCC
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
SARGVCKVMC FHPWSDVTLP LMSVPEIRAV VDAWASVTEE LGAQYPWVQI FENKGAMMGC
SNPHPHCQVW ASSFLPDIAQ REERSQQAYK SQHGEPLLME YSRQELLRKE RLVLTSEHWL
VLVPFWATWP YQTLLLPRRH VPRLPELTPA ERDDLASIMK KLLTKYDNLF ETSFPYSMGW
HGAPTGSEAG ANWNHWQLHA HYYPPLLRSA TVRKFMVGYE MLAQAQRDLT PEQAAERLRA
LPEVHYHLGQ KDRETATIA*
speed 1.00 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