Variant #0000498520 (NC_000005.9:g.125918566C>T, NM_001182.4:c.494G>T (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.125918566C>T
DNA change (hg38) g.126582874C>T
Published as -
ISCN -
DB-ID ALDH7A1_000135 See all 2 reported entries
Variant remarks expression cloning in E.coli shows no alpha‐AASADH activity
Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message.
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 N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH7A1 NM_001182.4 +/. - c.494G>T - p.Gln165Val


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