Variant #0000016498 (NC_000011.9:g.108005888_108005889delinsG, ACAT1(NM_000019.3):c.354_355delinsG)

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type Insertion/Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.108005888_108005889delinsG
Reference -
DB-ID ACAT1_000008
Frequency 1/59
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     
ACAT1 NM_000019.3 +?/+? 5 c.354_355delinsG r.0? Cys119Valfs*4