Variant #0001467757 (NC_000016.9:g.16127038_16127039insC, NC_000016.9(NM_004996.3):c.677+11_677+12insC (ABCC1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.16127038_16127039insC
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC1_000034
Frequency 81/11680
Freq. EA 0/7932
Freq. AA 81/3748
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 16:42:42 +02:00 (CEST)
Date last edited 2024-04-30 00:51:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC1 NM_004996.3 ?/? c.677+11_677+12insC r.(=) p.(=)