Yum, tasty mutations...

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999999998501088      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs3595 (probable pathogenic)
  • known disease mutation at this position (HGMD CM970026)
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr1:76205773A>GN/A show variant in all transcripts   IGV
HGNC symbol ACADM
Ensembl transcript ID ENST00000370834
Genbank transcript ID N/A
UniProt peptide P11310
alteration type single base exchange
alteration region CDS
DNA changes c.676A>G
cDNA.755A>G
g.15738A>G
AA changes T226A Score: 58 explain score(s)
position(s) of altered AA
if AA alteration in CDS
226
frameshift no
known variant Reference ID: rs121434279
Allele 'G' was neither found in ExAC nor 1000G.
known as potential disease variant: rs3595 (probable pathogenic for Medium-chain acyl-coenzyme A dehydrogenase deficiency) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM970026)

known disease mutation at this position, please check HGMD for details (HGMD ID CM970026)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970026)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)1.3681
4.941
(flanking)5.9841
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor marginally increased15741wt: 0.8986 / mu: 0.9181 (marginal change - not scored)wt: TAACCAACGGAGGAA
mu: TAGCCAACGGAGGAA
 ACCA|acgg
Donor gained157370.70mu: TGGATAGCCAACGGA GATA|gcca
Donor gained157320.40mu: AGATGTGGATAGCCA ATGT|ggat
distance from splice site 23
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      226EYIINGQKMWITNGGKANWYFLLA
mutated  not conserved    226EYIINGQKMWIANGGKANWYFLL
Ptroglodytes  all identical  ENSPTRG00000000871  193EYIINGQKMWITNGGKANWYFLL
Mmulatta  all identical  ENSMMUG00000007220  226EYIINGQKMWITNGGKASWYFLL
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000062908  193EYVINGQKMWITNGGKANWYFLL
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000007137  222EYVVNGQKMWITNGGKANWYFLL
Drerio  all identical  ENSDARG00000038900  198YVINGQKMWITNGGKANWYFLL
Dmelanogaster  all identical  FBgn0035811  189EWVINGQKMWITNGGVANWYFVL
Celegans  all identical  T08G2.3  183INGSKAWITGGGHAKWFFVL
Xtropicalis  all identical  ENSXETG00000002983  198EYIINGQKMWITNGGKANWYFLL
protein features
start (aa)end (aa)featuredetails 
219225STRANDmight get lost (downstream of altered splice site)
231233STRANDmight get lost (downstream of altered splice site)
237237MUTAGENE->A: Strongly reduced rate of electron transfer to ETF.might get lost (downstream of altered splice site)
239241STRANDmight get lost (downstream of altered splice site)
247258STRANDmight get lost (downstream of altered splice site)
259261HELIXmight get lost (downstream of altered splice site)
262265STRANDmight get lost (downstream of altered splice site)
266268TURNmight get lost (downstream of altered splice site)
269303HELIXmight get lost (downstream of altered splice site)
278281REGIONSubstrate binding.might get lost (downstream of altered splice site)
279279MOD_RESN6-acetyllysine.might get lost (downstream of altered splice site)
301301MOD_RESN6-acetyllysine.might get lost (downstream of altered splice site)
306308NP_BINDFAD.might get lost (downstream of altered splice site)
309312STRANDmight get lost (downstream of altered splice site)
313315HELIXmight get lost (downstream of altered splice site)
316317NP_BINDFAD.might get lost (downstream of altered splice site)
317345HELIXmight get lost (downstream of altered splice site)
351376HELIXmight get lost (downstream of altered splice site)
356356CONFLICTI -> T (in Ref. 3; AAF63626).might get lost (downstream of altered splice site)
374378NP_BINDFAD.might get lost (downstream of altered splice site)
377379HELIXmight get lost (downstream of altered splice site)
384384MUTAGENE->A: Reduces rate of electron transfer to ETF three-fold.might get lost (downstream of altered splice site)
384384MUTAGENE->Q: Reduces rate of electron transfer to ETF two-fold.might get lost (downstream of altered splice site)
387394HELIXmight get lost (downstream of altered splice site)
395398HELIXmight get lost (downstream of altered splice site)
399401TURNmight get lost (downstream of altered splice site)
401401ACT_SITEProton acceptor.might get lost (downstream of altered splice site)
402402BINDINGSubstrate; via amide nitrogen.might get lost (downstream of altered splice site)
403405NP_BINDFAD.might get lost (downstream of altered splice site)
404417HELIXmight get lost (downstream of altered splice site)
413413BINDINGSubstrate.might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1365 / 1365
position (AA) of stopcodon in wt / mu AA sequence 455 / 455
position of stopcodon in wt / mu cDNA 1444 / 1444
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 80 / 80
chromosome 1
strand 1
last intron/exon boundary 1373
theoretical NMD boundary in CDS 1243
length of CDS 1365
coding sequence (CDS) position 676
cDNA position
(for ins/del: last normal base / first normal base)
755
gDNA position
(for ins/del: last normal base / first normal base)
15738
chromosomal position
(for ins/del: last normal base / first normal base)
76205773
original gDNA sequence snippet ATGGTCAGAAGATGTGGATAACCAACGGAGGAAAAGCTAAT
altered gDNA sequence snippet ATGGTCAGAAGATGTGGATAGCCAACGGAGGAAAAGCTAAT
original cDNA sequence snippet ATGGTCAGAAGATGTGGATAACCAACGGAGGAAAAGCTAAT
altered cDNA sequence snippet ATGGTCAGAAGATGTGGATAGCCAACGGAGGAAAAGCTAAT
wildtype AA sequence MAAGFGRCCR VLRSISRFHW RSQHTKANRQ REPGLGFSFE FTEQQKEFQA TARKFAREEI
IPVAAEYDKT GEYPVPLIRR AWELGLMNTH IPENCDYSVC PLLEACTLYL DAFFLLLTGS
NLNLHLNLGG LGLGTFDACL ISEELAYGCT GVQTAIEGNS LGQMPIIIAG NDQQKKKYLG
RMTEEPLMCA YCVTEPGAGS DVAGIKTKAE KKGDEYIING QKMWITNGGK ANWYFLLARS
DPDPKAPANK AFTGFIVEAD TPGIQIGRKE LNMGQRCSDT RGIVFEDVKV PKENVLIGDG
AGFKVAMGAF DKTRPVVAAG AVGLAQRALD EATKYALERK TFGKLLVEHQ AISFMLAEMA
MKVELARMSY QRAAWEVDSG RRNTYYASIA KAFAGDIANQ LATDAVQILG GNGFNTEYPV
EKLMRDAKIY QIYEGTSQIQ RLIVAREHID KYKN*
mutated AA sequence MAAGFGRCCR VLRSISRFHW RSQHTKANRQ REPGLGFSFE FTEQQKEFQA TARKFAREEI
IPVAAEYDKT GEYPVPLIRR AWELGLMNTH IPENCDYSVC PLLEACTLYL DAFFLLLTGS
NLNLHLNLGG LGLGTFDACL ISEELAYGCT GVQTAIEGNS LGQMPIIIAG NDQQKKKYLG
RMTEEPLMCA YCVTEPGAGS DVAGIKTKAE KKGDEYIING QKMWIANGGK ANWYFLLARS
DPDPKAPANK AFTGFIVEAD TPGIQIGRKE LNMGQRCSDT RGIVFEDVKV PKENVLIGDG
AGFKVAMGAF DKTRPVVAAG AVGLAQRALD EATKYALERK TFGKLLVEHQ AISFMLAEMA
MKVELARMSY QRAAWEVDSG RRNTYYASIA KAFAGDIANQ LATDAVQILG GNGFNTEYPV
EKLMRDAKIY QIYEGTSQIQ RLIVAREHID KYKN*
speed 0.96 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