Variant #0000016281 (NC_000012.11:g.121176239T>A, ACADS(NM_000017.2):c.781T>A)

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.121176239T>A
Reference weizhou et al. (2021)
DB-ID ACADS_000018
Frequency 1/179
Variant remarks -
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner ting zhang
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by ting zhang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADS NM_000017.2 ?/? 6 c.781T>A r.0? Phe261Ile