Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999995914617      (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 ENST00000543667
Genbank transcript ID N/A
UniProt peptide P11310
alteration type single base exchange
alteration region CDS
DNA changes c.10A>G
cDNA.328A>G
g.15738A>G
AA changes T4A Score: 58 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 4
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      4 MWITNGGKANWYFLLA
mutated  not conserved    4 MWIANGGKANWYFLLARSDPDP
Ptroglodytes  all identical  ENSPTRG00000000871  193 MWITNGGKANWYFLLARSDPDP
Mmulatta  all identical  ENSMMUG00000007220  226 MWITNGGKASWYFLLARSDPDP
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000062908  193 MWITNGGKANWYFLLARSNPDP
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000007137  222 MWITNGGKANWYFLLARTNPDP
Drerio  all identical  ENSDARG00000038900  198 MWITNGGKANWYFLLARTDSDP
Dmelanogaster  all identical  FBgn0035811  189 MWITNGGVANWYFVLARTNPDP
Celegans  all identical  T08G2.3  183 WITGGGHAKWFFVLARSDPNP
Xtropicalis  all identical  ENSXETG00000002983  198 MWITNGGKANWYFLLARTNPDP
protein features
start (aa)end (aa)featuredetails 
125TRANSITMitochondrion.lost
3638STRANDmight get lost (downstream of altered splice site)
4359HELIXmight get lost (downstream of altered splice site)
6170HELIXmight get lost (downstream of altered splice site)
7584HELIXmight get lost (downstream of altered splice site)
8686MUTAGENL->M: Strongly reduced rate of electron transfer to ETF.might get lost (downstream of altered splice site)
9395HELIXmight get lost (downstream of altered splice site)
9898MUTAGENL->W: Strongly reduced rate of electron transfer to ETF.might get lost (downstream of altered splice site)
100100MUTAGENL->Y: Strongly reduced rate of electron transfer to ETF.might get lost (downstream of altered splice site)
102115HELIXmight get lost (downstream of altered splice site)
108108MUTAGENI->M: Strongly reduced rate of electron transfer to ETF.might get lost (downstream of altered splice site)
117129HELIXmight get lost (downstream of altered splice site)
131136HELIXmight get lost (downstream of altered splice site)
139151HELIXmight get lost (downstream of altered splice site)
156159STRANDmight get lost (downstream of altered splice site)
158167NP_BINDFAD.might get lost (downstream of altered splice site)
165168STRANDmight get lost (downstream of altered splice site)
167167BINDINGSubstrate; via carbonyl oxygen.might get lost (downstream of altered splice site)
169171HELIXmight get lost (downstream of altered splice site)
175178STRANDmight get lost (downstream of altered splice site)
180193STRANDmight get lost (downstream of altered splice site)
191191MUTAGENW->A: Loss of electron transfer to ETF.might get lost (downstream of altered splice site)
191191MUTAGENW->F: Reduces rate of electron transfer to ETF about six-fold.might get lost (downstream of altered splice site)
191193NP_BINDFAD.might get lost (downstream of altered splice site)
194197TURNmight get lost (downstream of altered splice site)
199206STRANDmight get lost (downstream of altered splice site)
212212MOD_RESN6-acetyllysine.might get lost (downstream of altered splice site)
215217HELIXmight get lost (downstream of altered splice site)
216216BINDINGSubstrate.might get lost (downstream of altered splice site)
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->Q: Reduces rate of electron transfer to ETF two-fold.might 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)
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 699 / 699
position (AA) of stopcodon in wt / mu AA sequence 233 / 233
position of stopcodon in wt / mu cDNA 1017 / 1017
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 319 / 319
chromosome 1
strand 1
last intron/exon boundary 946
theoretical NMD boundary in CDS 577
length of CDS 699
coding sequence (CDS) position 10
cDNA position
(for ins/del: last normal base / first normal base)		 328
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 MWITNGGKAN WYFLLARSDP DPKAPANKAF TGFIVEADTP GIQIGRKELN MGQRCSDTRG
IVFEDVKVPK ENVLIGDGAG FKVAMGAFDK TRPVVAAGAV GLAQRALDEA TKYALERKTF
GKLLVEHQAI SFMLAEMAMK VELARMSYQR AAWEVDSGRR NTYYASIAKA FAGDIANQLA
TDAVQILGGN GFNTEYPVEK LMRDAKIYQI YEGTSQIQRL IVAREHIDKY KN*
mutated AA sequence MWIANGGKAN WYFLLARSDP DPKAPANKAF TGFIVEADTP GIQIGRKELN MGQRCSDTRG
IVFEDVKVPK ENVLIGDGAG FKVAMGAFDK TRPVVAAGAV GLAQRALDEA TKYALERKTF
GKLLVEHQAI SFMLAEMAMK VELARMSYQR AAWEVDSGRR NTYYASIAKA FAGDIANQLA
TDAVQILGGN GFNTEYPVEK LMRDAKIYQI YEGTSQIQRL IVAREHIDKY KN*
speed 0.55 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