Variant #0000000295 (NC_000016.9:g.1412221del, NM_032520.4:c.426del (GNPTG))
| Individual ID |
00000081 |
| Chromosome |
16 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1412221del |
| Reference |
- |
| DB-ID |
GNPTG_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 |
| Date created |
2020-12-21 21:23:04 +00:00 (UTC) |
| Date last edited |
2021-05-11 00:35:24 +00:00 (UTC) |

Variant on transcripts
Screenings
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