Variant #0001291374 (NC_000013.10:g.95862896A>G, NC_000013.10(NM_005845.3):c.621+50T>C (ABCC4))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.95862896A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC4_000247
Frequency 9681/13006
Freq. EA 6982/8600
Freq. AA 2699/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:41:01 +02:00 (CEST)
Date last edited 2024-12-14 20:26:26 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC4 NM_005845.3 ?/? c.621+50T>C r.(=) p.(=)