Variant #0000016549 (NC_000012.11:g.121176140_121176141del, ACADS(NM_000017.2):c.682_683del)

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.121176140_121176141del
Reference Chiju Yang et al. (2021)
DB-ID ACADS_000016
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.682_683del r.(?) p.(Glu228Argfs*16)