Variant #0000000604 (NC_000011.9:g.17474683_17474684del, NM_000352.3:c.1158_1159del (ABCC8))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.17474683_17474684del
Reference -
DB-ID ABCC8_000008
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Admin
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Admin
Date created 2024-07-29 06:12:08 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCC8 NM_000352.3 ?/? 8 c.1158_1159del r.(?) p.(Leu387Glufs*11)