Variant #0000000022 (NC_000014.8:g.21762926_21762927insGGTGAAG, RPGRIP1(NM_020366.3):c.176_177insGGTGAAG)
Individual ID |
00000024 |
Chromosome |
14 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.21762926_21762927insGGTGAAG |
Reference |
- |
DB-ID |
RPGRIP1_000001 |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
variome.ir |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
variome.ir |
Variant on transcripts
Screenings
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