Variant #0000988559 (NC_000010.10:g.50732155_50732157del, NM_000124.2:c.1319_1321del (ERCC6))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.50732155_50732157del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC6_000282
Frequency 5/12518
Freq. EA 4/8254
Freq. AA 1/4264
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 16:30:47 +02:00 (CEST)
Date last edited 2013-05-04 19:21:22 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC6 NM_000124.2 ?/? c.1319_1321del r.(?) p.(Gly440del)
PGBD3 NM_170753.2 ?/? c.-86_-84del r.(?) p.(Gly440del)