Variant #0000268342 (NC_000002.11:g.128038128_128038129insT, NM_000122.1:c.1421_1422insA (ERCC3))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.128038128_128038129insT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC3_000058
Frequency 5/12520
Freq. EA 5/8254
Freq. AA 0/4266
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 16:22:05 +02:00 (CEST)
Date last edited 2013-05-03 23:23:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC3 NM_000122.1 ?/? c.1421_1422insA r.(?) p.(Asp474Glufs*2)