Variant #0000498524 (NC_000005.9:g.125918591C>G, NM_001182.4:c.469G>C (ALDH7A1))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.125918591C>G
DNA change (hg38) g.126582899C>G
Published as -
ISCN -
DB-ID ALDH7A1_000137
Variant remarks expression cloning in E.coli shows no alpha‐AASADH activity
Reference PubMed: Korasick 2017
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Curtis Coughlin II
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-06-11 17:50:42 +02:00 (CEST)
Date last edited 2020-06-17 14:49:17 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH7A1 NM_001182.4 +/. - c.469G>C r.(?) p.Ala157Pro


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