Variant #0000000050 (NC_000003.11:g.100951806C>T, IMPG2(NM_016247.3):c.3052G>A)
Individual ID |
00000069 |
Chromosome |
3 |
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.100951806C>T |
Reference |
- |
DB-ID |
IMPG2_000003 |
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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