Variant #0000394380 (NC_000016.9:g.1411799G>A, NC_000016.9(NM_032520.4):c.233+1G>A (GNPTG))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1411799G>A |
| DNA change (hg38) |
g.1361798G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GNPTG_000081 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline/De novo (untested) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
Renata Voltolini Velho |
| Database submission license |
No license selected |
| Created by |
Renata Voltolini Velho |
| Date created |
2018-07-30 10:35:20 +02:00 (CEST) |
| Date last edited |
2020-07-07 12:46:12 +02:00 (CEST) |

Variant on transcripts
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