Variant #0001295475 (NC_000013.10:g.103508379G>C, NC_000013.10(NM_000123.3):c.468-23G>C (ERCC5))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.103508379G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC5_000034
Frequency 3/13006
Freq. EA 3/8600
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 16:41:01 +02:00 (CEST)
Date last edited 2013-05-05 06:21:23 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC5 NM_000123.3 ?/? c.468-23G>C r.(=) p.(=)