Variant #0000016671 (NC_000011.9:g.108009665_108018370del, ACAT1(NM_000019.3):c.476_*253del)

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.108009665_108018370del
Reference -
DB-ID ACAT1_000012
Frequency 2/59
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACAT1 NM_000019.3 +/+ 6i_12i c.476_*253del r.(?) p.(Val159_Leu427delinsAspMetValGluIleProMetCysAsnIleSerAspLeuHisLys)