Variant #0001781802 (NC_000019.9:g.45864873C>G, NM_000400.3:c.1146G>C (ERCC2))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.45864873C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC2_000168
Frequency 1/13006
Freq. EA 1/8600
Freq. AA 0/4406
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 2013-05-06 01:48:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC2 NM_000400.3 ?/? c.1146G>C r.(=) p.(=)