Variant #0001295503 (NC_000013.10:g.103514091T>C, NC_000013.10(NM_000123.3):c.880+27T>C (ERCC5))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.103514091T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC5_000062
Frequency 12972/13002
Freq. EA 8600/8600
Freq. AA 4372/4402
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 16:41:01 +02:00 (CEST)
Date last edited 2019-09-19 21:20:04 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC5 NM_000123.3 ?/? c.880+27T>C r.(=) p.(=)