Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999931844192      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs7912 (probable pathogenic)
  • known disease mutation at this position (HGMD CM000298)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr1:94480221G>CN/A show variant in all transcripts   IGV
HGNC symbol ABCA4
Ensembl transcript ID ENST00000536513
Genbank transcript ID N/A
UniProt peptide P78363
alteration type single base exchange
alteration region CDS
DNA changes c.148C>G
cDNA.241C>G
g.106468C>G
AA changes P50A Score: 27 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 50
frameshift no
known variant Reference ID: rs121909207
databasehomozygous (C/C)heterozygousallele carriers
1000G---
ExAC01414

known as potential disease variant: rs7912 (probable pathogenic for Retinal dystrophy|Stargardt disease 1|ABCA4-Related Disorders|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM000298)

known disease mutation at this position, please check HGMD for details (HGMD ID CM000298)
known disease mutation at this position, please check HGMD for details (HGMD ID CM000298)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.8291
5.8291
(flanking)0.5461
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor gained1064670.68mu: ATGTACGCAGCATCC GTAC|gcag
distance from splice site 26
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      50LYGWAVIPMMYPASFLFDVPSTAY
mutated  not conserved    50LYGWAVIPMMYAASFLFDVPST
Ptroglodytes  all identical  ENSPTRG00000023377  1780LYGWAVIPMMYPASFLFDVPSTA
Mmulatta  no alignment  ENSMMUG00000013858  n/a
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000028125  1779LYGWAVIPMMYPASFLFEVPSTA
Ggallus  all identical  ENSGALG00000005752  1774LYGWAAIPMMYPASSFFSVPSTA
Trubripes  no homologue    
Drerio  all identical  ENSDARG00000062661  1845LYGWSVTPMMYPLSYMFNVPSTA
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000008223  1855FYGWAVIPMMYPASYLFNVPSTA
protein features
start (aa)end (aa)featuredetails 
43646TOPO_DOMExtracellular.lost
7575DISULFIDBy similarity.might get lost (downstream of altered splice site)
9898CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
324324DISULFIDBy similarity.might get lost (downstream of altered splice site)
415415CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
444444CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
504504CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
647667TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
700720TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
722722CONFLICTG -> V (in Ref. 2; AAC23915).might get lost (downstream of altered splice site)
731751TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
760780TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
836856TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
849849CONFLICTV -> C (in Ref. 1; AAC51144).might get lost (downstream of altered splice site)
8571376TOPO_DOMCytoplasmic.might get lost (downstream of altered splice site)
882882CONFLICTG -> S (in Ref. 1; AAC51144 and 3; CAA75729).might get lost (downstream of altered splice site)
9291160DOMAINABC transporter 1.might get lost (downstream of altered splice site)
941941CONFLICTC -> S (in Ref. 2; AAC23915).might get lost (downstream of altered splice site)
963970NP_BINDATP 1 (Potential).might get lost (downstream of altered splice site)
966966MUTAGENG->D: Abolishes basal and retinal- stimulated ATP hydrolysis.might get lost (downstream of altered splice site)
969969MUTAGENK->M: Abolishes basal and retinal- stimulated ATP hydrolysis.might get lost (downstream of altered splice site)
11161116CONFLICTS -> P (in Ref. 1; AAC51144).might get lost (downstream of altered splice site)
11251126CONFLICTLL -> HQ (in Ref. 1; AAC51144).might get lost (downstream of altered splice site)
13771397TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
13951395CONFLICTP -> L (in Ref. 1; AAC51144 and 3; CAA75729).might get lost (downstream of altered splice site)
13981727TOPO_DOMExtracellular.might get lost (downstream of altered splice site)
14651465CONFLICTS -> C (in Ref. 4; AAC05632).might get lost (downstream of altered splice site)
14691469CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
14881488DISULFIDBy similarity.might get lost (downstream of altered splice site)
15021502DISULFIDBy similarity.might get lost (downstream of altered splice site)
15181518CONFLICTS -> T (in Ref. 4; AAC05632).might get lost (downstream of altered splice site)
15291529CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
15881588CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
16621662CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
17281748TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
17331733CONFLICTM -> V (in Ref. 2; AAC23915).might get lost (downstream of altered splice site)
17601780TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
17931813TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
18321852TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
18741894TRANSMEMHelical; (Potential).might get lost (downstream of altered splice site)
18952273TOPO_DOMCytoplasmic.might get lost (downstream of altered splice site)
19382170DOMAINABC transporter 2.might get lost (downstream of altered splice site)
19721979NP_BINDATP 2 (Potential).might get lost (downstream of altered splice site)
19751975MUTAGENG->D: Inhibition of retinal-stimulated ATP hydrolysis.might get lost (downstream of altered splice site)
19781978MUTAGENK->M: Inhibition of retinal-stimulated ATP hydrolysis.might get lost (downstream of altered splice site)
19891989CONFLICTT -> N (in Ref. 2; AAC23915).might get lost (downstream of altered splice site)
21192119CONFLICTE -> K (in Ref. 1; AAC51144).might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1632 / 1632
position (AA) of stopcodon in wt / mu AA sequence 544 / 544
position of stopcodon in wt / mu cDNA 1725 / 1725
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 94 / 94
chromosome 1
strand -1
last intron/exon boundary 1720
theoretical NMD boundary in CDS 1576
length of CDS 1632
coding sequence (CDS) position 148
cDNA position
(for ins/del: last normal base / first normal base)		 241
gDNA position
(for ins/del: last normal base / first normal base)		 106468
chromosomal position
(for ins/del: last normal base / first normal base)		 94480221
original gDNA sequence snippet CGGTCATTCCCATGATGTACCCAGCATCCTTCCTGTTTGAT
altered gDNA sequence snippet CGGTCATTCCCATGATGTACGCAGCATCCTTCCTGTTTGAT
original cDNA sequence snippet CGGTCATTCCCATGATGTACCCAGCATCCTTCCTGTTTGAT
altered cDNA sequence snippet CGGTCATTCCCATGATGTACGCAGCATCCTTCCTGTTTGAT
wildtype AA sequence MMMNYSVSAG LVVGIFIGFQ KKAYTSPENL PALVALLLLY GWAVIPMMYP ASFLFDVPST
AYVALSCANL FIGINSSAIT FILELFENNR TLLRFNAVLR KLLIVFPHFC LGRGLIDLAL
SQAVTDVYAR FGEEHSANPF HWDLIGKNLF AMVVEGVVYF LLTLLVQRHF FLSQWIAEPT
KEPIVDEDDD VAEERQRIIT GGNKTDILRL HELTKIYPGT SSPAVDRLCV GVRPGECFGL
LGVNGAGKTT TFKMLTGDTT VTSGDATVAG KSILTNISEV HQNMGYCPQF DAIDELLTGR
EHLYLYARLR GVPAEEIEKV ANWSIKSLGL TVYADCLAGT YSGGNKRKLS TAIALIGCPP
LVLLDEPTTG MDPQARRMLW NVIVSIIREG RAVVLTSHSM EECEALCTRL AIMVKGAFRC
MGTIQHLKSK FGDGYIVTMK IKSPKDDLLP DLNPVEQFFQ GNFPGSVQRE RHYNMLQFQV
SSSSLARIFQ LLLSHKDSLL IEEYSVTQTT LDQVFVNFAK QQTESHDLPL HPRAAGASRQ
AQD*
mutated AA sequence MMMNYSVSAG LVVGIFIGFQ KKAYTSPENL PALVALLLLY GWAVIPMMYA ASFLFDVPST
AYVALSCANL FIGINSSAIT FILELFENNR TLLRFNAVLR KLLIVFPHFC LGRGLIDLAL
SQAVTDVYAR FGEEHSANPF HWDLIGKNLF AMVVEGVVYF LLTLLVQRHF FLSQWIAEPT
KEPIVDEDDD VAEERQRIIT GGNKTDILRL HELTKIYPGT SSPAVDRLCV GVRPGECFGL
LGVNGAGKTT TFKMLTGDTT VTSGDATVAG KSILTNISEV HQNMGYCPQF DAIDELLTGR
EHLYLYARLR GVPAEEIEKV ANWSIKSLGL TVYADCLAGT YSGGNKRKLS TAIALIGCPP
LVLLDEPTTG MDPQARRMLW NVIVSIIREG RAVVLTSHSM EECEALCTRL AIMVKGAFRC
MGTIQHLKSK FGDGYIVTMK IKSPKDDLLP DLNPVEQFFQ GNFPGSVQRE RHYNMLQFQV
SSSSLARIFQ LLLSHKDSLL IEEYSVTQTT LDQVFVNFAK QQTESHDLPL HPRAAGASRQ
AQD*
speed 0.32 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