Variant #0000000953 (NC_000010.10:g.50681659T>C, ERCC6(NM_000124.3):c.2599-26A>G)
Individual ID |
00000953 |
Chromosome |
10 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.50681659T>C |
Reference |
Laugel V1, Dalloz C, Durand M, Sauvanaud F, Kristensen U, Vincent MC, Pasquier L, Odent S, Cormier-Daire V, Gener B, Tobias ES, Tolmie JL, Martin-Coignard D, Drouin-Garraud V,(2010) |
DB-ID |
ERCC6_000066 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
5.0E-5 View details |
Owner |
Y Yang |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Y Yang |
Variant on transcripts
Screenings
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