Variant #0000000028 (NC_000010.10:g.55700727G>A, PCDH15(NM_001142772.1):c.3131C>T)
Individual ID |
00000036 |
Chromosome |
10 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.55700727G>A |
Reference |
- |
DB-ID |
PCDH15_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
|
|