Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999916678 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM960722)
  • known disease mutation: rs2082 (pathogenic)
  • protein features (might be) affected
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr19:13010300C>TN/A show variant in all transcripts   IGV
HGNC symbol GCDH
Ensembl transcript ID ENST00000422947
Genbank transcript ID N/A
UniProt peptide Q92947
alteration type single base exchange
alteration region CDS
DNA changes c.1130C>T
cDNA.1388C>T
g.8461C>T
AA changes A377V Score: 64 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 377
frameshift no
known variant Reference ID: rs121434367
databasehomozygous (T/T)heterozygousallele carriers
1000G---
ExAC02323

known disease mutation: rs2082 (pathogenic for Glutaric aciduria, type 1|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM960722)

known disease mutation at this position, please check HGMD for details (HGMD ID CM960722)
known disease mutation at this position, please check HGMD for details (HGMD ID CM960722)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.6051
5.6051
(flanking)-2.7490.021
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased8472wt: 0.2675 / mu: 0.3327 (marginal change - not scored)wt: ACATTCACGCCCTGATCCTTGGGAGAGCTATCACGGGAATC
mu: ACATTCACGTCCTGATCCTTGGGAGAGCTATCACGGGAATC		 cttg|GGAG
Donor marginally increased8454wt: 0.9706 / mu: 0.9861 (marginal change - not scored)wt: ATGACATTCACGCCC
mu: ATGACATTCACGTCC		 GACA|ttca
distance from splice site 19
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      377VNTYEGTHDIHALILGRAITGIQA
mutated  not conserved    377VNTYEGTHDIHVLILGRAITGIQ
Ptroglodytes  all identical  ENSPTRG00000010548  421VNTYEGTHDIHALILGRAITGIQ
Mmulatta  all identical  ENSMMUG00000007043  421VNTYEGTHDIHALILGRAITGIQ
Fcatus  all identical  ENSFCAG00000000477  421YEGTHDIHALILGRAITGIQ
Mmusculus  all identical  ENSMUSG00000003809  421VNTYEGTHDIHALILGRAITGIQ
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000008257  427VNTYEGTHDIHALILGRAITGLQ
Drerio  no alignment  ENSDARG00000038361  n/a
Dmelanogaster  all identical  FBgn0031824  404VNTYEGTHDIHALILGRAITGLA
Celegans  all identical  F54D5.7  395VNTYEGTHDVHALILGRAITGLN
Xtropicalis  all identical  ENSXETG00000007932  423VNTYEGTHDVHALILGRAITGLQ
protein features
start (aa)end (aa)featuredetails 
364388HELIXlost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1185 / 1185
position (AA) of stopcodon in wt / mu AA sequence 395 / 395
position of stopcodon in wt / mu cDNA 1443 / 1443
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 259 / 259
chromosome 19
strand 1
last intron/exon boundary 1370
theoretical NMD boundary in CDS 1061
length of CDS 1185
coding sequence (CDS) position 1130
cDNA position
(for ins/del: last normal base / first normal base)		 1388
gDNA position
(for ins/del: last normal base / first normal base)		 8461
chromosomal position
(for ins/del: last normal base / first normal base)		 13010300
original gDNA sequence snippet AGGTACACATGACATTCACGCCCTGATCCTTGGGAGAGCTA
altered gDNA sequence snippet AGGTACACATGACATTCACGTCCTGATCCTTGGGAGAGCTA
original cDNA sequence snippet AGGTACACATGACATTCACGCCCTGATCCTTGGGAGAGCTA
altered cDNA sequence snippet AGGTACACATGACATTCACGTCCTGATCCTTGGGAGAGCTA
wildtype AA sequence MRSSSGTPSA PTARRDSCLA SCWPIATKSL ALLPRLECSG TILAHCKFCL PGSSDSPAST
PLVAGITGYG CAGVSSVAYG LLARELERVD SGYRSAMSVQ SSLVMHPIYA YGSEEQRQKY
LPQLAKGELL GCFGLTEPNS GSDPSSMETR AHYNSSNKSY TLNGTKTWIT NSPMADLFVV
WARCEDGCIR GFLLEKGMRG LSAPRIQGKF SLRASATGMI IMDGVEVPEE NVLPGASSLG
GPFGCLNNAR YGIAWGVLGA SEFCLHTARQ YALDRMQFGV PLARNQLIQK KLADMLTEIT
LGLHACLQLG RLKDQDKAAP EMVSLLKRNN CGKALDIARQ ARDMLGGNGI SDEYHVIRHA
MNLEAVNTYE GTHDIHALIL GRAITGIQAF TASK*
mutated AA sequence MRSSSGTPSA PTARRDSCLA SCWPIATKSL ALLPRLECSG TILAHCKFCL PGSSDSPAST
PLVAGITGYG CAGVSSVAYG LLARELERVD SGYRSAMSVQ SSLVMHPIYA YGSEEQRQKY
LPQLAKGELL GCFGLTEPNS GSDPSSMETR AHYNSSNKSY TLNGTKTWIT NSPMADLFVV
WARCEDGCIR GFLLEKGMRG LSAPRIQGKF SLRASATGMI IMDGVEVPEE NVLPGASSLG
GPFGCLNNAR YGIAWGVLGA SEFCLHTARQ YALDRMQFGV PLARNQLIQK KLADMLTEIT
LGLHACLQLG RLKDQDKAAP EMVSLLKRNN CGKALDIARQ ARDMLGGNGI SDEYHVIRHA
MNLEAVNTYE GTHDIHVLIL GRAITGIQAF TASK*
speed 1.25 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