Variant #0000016234 (NC_000001.10:g.76200537_76200540del, ACADM(NM_000016.4):c.449_452del)

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.76200537_76200540del
Reference Benjing Wang et al. (2019)
DB-ID ACADM_000015
Frequency 32/130
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 +/+ 6 c.449_452del r.0? Thr150Argfs*4