Variant #0000016531 (NC_000001.10:g.76227044_76227046delinsTAT, ACADM(NM_000016.4):c.1183_1185delinsTAT)

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type Insertion/Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.76227044_76227046delinsTAT
Reference Shuting Wang et al. (2020)
DB-ID ACADM_000051
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.1183_1185delinsTAT r.(?) p.(Lys395Tyr)