Variant #0000016547 (NC_000012.11:g.121176670_121176672del, ACADS(NM_000017.2):c.981_983del)

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.121176670_121176672del
Reference Shuting Wang et al. (2020)
DB-ID ACADS_000024
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADS NM_000017.2 ?/? 8 c.981_983del r.(?) p.(Thr328del)