View genomic variant #0000016963

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.112241766G>A
Published as -
GERP -
Segregation -
DB-ID ALDH2_000001 See all 3 reported entries
MSCV MSCV_0000484
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
ALDH2 00000435 NM_000690.3 0000016963 ./. - - c.1510G>A p.(Glu504Lys) - - - -
ALDH2 00000436 NM_001204889.1 0000016963 ./. - - c.1369G>A p.(Glu457Lys) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000020061; RCV000020060; RCV000020062; RCV000020058; RCV000020059; RCV001290000; RCV001787815;
Chromosome 12:112241766..112241766
Allele frequencies from ExAC 0.02129
Allele frequencies from TGP 0.03574
ClinVar Allele ID 33429
Disease database name and identifier MONDO:MONDO:0012454, MedGen:C2674838, OMIM:610251|MedGen:C2608086|MedGen:C2676227|MedGen:C3149226|.|MONDO:MONDO:0030894, MedGen:C5436906, OMIM:619151, Orphanet:611216|Human Phenotype Ontology:HP:0030955, MONDO:MONDO:0007079, MedGen:C0001973, OMIM:103780
ClinVar preferred disease name Alcohol sensitivity, acute|Susceptibility to hangover|Sublingual nitroglycerin, susceptibility to poor response to|Esophageal cancer, alcohol-related, susceptibility to|ethanol response - Toxicity|AMED syndrome, digenic|Addictive alcohol use
HGVS variant names NC 000012.11:g.112241766G>A
ClinVar review status reviewed by expert panel
Clinical Significance drug response
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA128085|OMIM:100650.0001|UniProtKB:P05091#VAR 002248
Gene symbol:Gene id. ALDH2:217
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 671
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None