Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999997243089 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM980012)
  • known disease mutation: rs1632 (pathogenic)
  • protein features (might be) affected
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr17:7127326T>CN/A show variant in all transcripts   IGV
HGNC symbol ACADVL
Ensembl transcript ID ENST00000350303
Genbank transcript ID NM_001033859
UniProt peptide P49748
alteration type single base exchange
alteration region CDS
DNA changes c.1306T>C
cDNA.1428T>C
g.6883T>C
AA changes F436L Score: 22 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 436
frameshift no
known variant Reference ID: rs118204017
Allele 'C' was neither found in ExAC nor 1000G.
known disease mutation: rs1632 (pathogenic for Very long chain acyl-CoA dehydrogenase deficiency) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM980012)

known disease mutation at this position, please check HGMD for details (HGMD ID CM980012)
known disease mutation at this position, please check HGMD for details (HGMD ID CM980012)
regulatory features Promoter Associated, Regulatory Feature, Promoter like regulatory feature
PolII, Polymerase, RNA Polymerase II
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
Gene Associated, Regulatory Feature, Gene associated regulatory feature
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
DNase1, Open Chromatin, DNase1 Hypersensitive Site
phyloP / phastCons
PhyloPPhastCons
(flanking)1.591
3.8951
(flanking)3.8951
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 40
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      436GVERVLRDLRIFRIFEGTNDILRL
mutated  not conserved    436GVERVLRDLRILRIFEGTNDILR
Ptroglodytes  all identical  ENSPTRG00000008664  481GVERVLRDLRVFRIFEGTNDILR
Mmulatta  all identical  ENSMMUG00000010538  478GVERVLRDLRIF
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000018574  459GVERVLRDIRIFRIFEGANDILR
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000013710  460GVERVMRDLRIFRIFEGTNDILR
Drerio  all identical  ENSDARG00000016687  463GVERVLRDLRIFRIFEGTNDILR
Dmelanogaster  all identical  FBgn0034432  431GLERVLRDLRIFRIFEGTNDILR
Celegans  all identical  E04F6.5  426GLERVLRDLRIFRIFEGANDVLR
Xtropicalis  not conserved  ENSXETG00000031271  255--NRCICSLHCCGLIPWAINPFL-
protein features
start (aa)end (aa)featuredetails 
41482REGIONCatalytic.lost
412437HELIXlost
435439NP_BINDFAD (By similarity).lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1902 / 1902
position (AA) of stopcodon in wt / mu AA sequence 634 / 634
position of stopcodon in wt / mu cDNA 2024 / 2024
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 123 / 123
chromosome 17
strand 1
last intron/exon boundary 1884
theoretical NMD boundary in CDS 1711
length of CDS 1902
coding sequence (CDS) position 1306
cDNA position
(for ins/del: last normal base / first normal base)		 1428
gDNA position
(for ins/del: last normal base / first normal base)		 6883
chromosomal position
(for ins/del: last normal base / first normal base)		 7127326
original gDNA sequence snippet TGCTCCGAGATCTTCGCATCTTCCGGATCTTTGAGGGGACA
altered gDNA sequence snippet TGCTCCGAGATCTTCGCATCCTCCGGATCTTTGAGGGGACA
original cDNA sequence snippet TGCTCCGAGATCTTCGCATCTTCCGGATCTTTGAGGGGACA
altered cDNA sequence snippet TGCTCCGAGATCTTCGCATCCTCCGGATCTTTGAGGGGACA
wildtype AA sequence MQAARMAASL GRQLLRLGGG SSRLTALLGQ PRPGPARRPY AGGAAQESKS FAVGMFKGQL
TTDQVFPYPS VLNEEQTQFL KELVEPVSRF FEEVNDPAKN DALEMVEETT WQGLKELGAF
GLQVPSELGG VGLCNTQYAR LVEIVGMHDL GVGITLGAHQ SIGFKGILLF GTKAQKEKYL
PKLASGETVA AFCLTEPSSG SDAASIRTSA VPSPCGKYYT LNGSKLWISN GGLADIFTVF
AKTPVTDPAT GAVKEKITAF VVERGFGGIT HGPPEKKMGI KASNTAEVFF DGVRVPSENV
LGEVGSGFKV AMHILNNGRF GMAAALAGTM RGIIAKAVDH ATNRTQFGEK IHNFGLIQEK
LARMVMLQYV TESMAYMVSA NMDQGATDFQ IEAAISKIFG SEAAWKVTDE CIQIMGGMGF
MKEPGVERVL RDLRIFRIFE GTNDILRLFV ALQGCMDKGK ELSGLGSALK NPFGNAGLLL
GEAGKQLRRR AGLGSGLSLS GLVHPELSRS GELAVRALEQ FATVVEAKLI KHKKGIVNEQ
FLLQRLADGA IDLYAMVVVL SRASRSLSEG HPTAQHEKML CDTWCIEAAA RIREGMAALQ
SDPWQQELYR NFKSISKALV ERGGVVTSNP LGF*
mutated AA sequence MQAARMAASL GRQLLRLGGG SSRLTALLGQ PRPGPARRPY AGGAAQESKS FAVGMFKGQL
TTDQVFPYPS VLNEEQTQFL KELVEPVSRF FEEVNDPAKN DALEMVEETT WQGLKELGAF
GLQVPSELGG VGLCNTQYAR LVEIVGMHDL GVGITLGAHQ SIGFKGILLF GTKAQKEKYL
PKLASGETVA AFCLTEPSSG SDAASIRTSA VPSPCGKYYT LNGSKLWISN GGLADIFTVF
AKTPVTDPAT GAVKEKITAF VVERGFGGIT HGPPEKKMGI KASNTAEVFF DGVRVPSENV
LGEVGSGFKV AMHILNNGRF GMAAALAGTM RGIIAKAVDH ATNRTQFGEK IHNFGLIQEK
LARMVMLQYV TESMAYMVSA NMDQGATDFQ IEAAISKIFG SEAAWKVTDE CIQIMGGMGF
MKEPGVERVL RDLRILRIFE GTNDILRLFV ALQGCMDKGK ELSGLGSALK NPFGNAGLLL
GEAGKQLRRR AGLGSGLSLS GLVHPELSRS GELAVRALEQ FATVVEAKLI KHKKGIVNEQ
FLLQRLADGA IDLYAMVVVL SRASRSLSEG HPTAQHEKML CDTWCIEAAA RIREGMAALQ
SDPWQQELYR NFKSISKALV ERGGVVTSNP LGF*
speed 1.02 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