Variant #0001055314 (NC_000016.9:g.1402251_1402267del, NM_032520.4:c.122_138del (GNPTG))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1402251_1402267del |
| DNA change (hg38) |
- |
| Published as |
GNPTG(NM_032520.5):c.122_138del (p.(Pro41Glnfs*36)) |
| ISCN |
- |
| DB-ID |
GNPTG_000039 See all 2 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2025-11-01 13:22:20 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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