Variant #0001465561 (NC_000016.9:g.14026168A>G, NC_000016.9(NM_005236.2):c.1102+26A>G (ERCC4))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.14026168A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC4_000068
Frequency 1/12904
Freq. EA 1/8564
Freq. AA 0/4340
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 2018-01-14 19:39:06 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC4 NM_005236.2 ?/? c.1102+26A>G r.(=) p.(=)