Variant #0000000023 (NC_000016.9:g.57949164G>A, CNGB1(NM_001297.4):c.2293C>T)
Individual ID |
00000026 |
Chromosome |
16 |
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.57949164G>A |
Reference |
- |
DB-ID |
CNGB1_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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