Variant #0001781858 (NC_000019.9:g.45868315G>C, NM_000400.3:c.462C>G (ERCC2))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.45868315G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC2_000224
Frequency 2/13006
Freq. EA 0/8600
Freq. AA 2/4406
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 16:45:39 +02:00 (CEST)
Date last edited 2024-12-15 17:14:35 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC2 NM_000400.3 ?/? c.462C>G r.(?) p.(His154Gln)