Variant #0000016253 (NC_000001.10:g.76226831_76226832delinsAT, ACADM(NM_000016.4):c.970_971delinsAT)

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Insertion/Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.76226831_76226832delinsAT
Reference Zhuwen Gong et al. (2021)
DB-ID ACADM_000040
Frequency 1/130
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     
ACADM NM_000016.4 +/. 11 c.970_971delinsAT r.0? Ala324Ile