Variant #0000973781 (NC_000001.10:g.235628971_235628972dup, NM_152490.3:c.824_825dup (B3GALNT2))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.235628971_235628972dup |
| DNA change (hg38) |
- |
| Published as |
B3GALNT2(NM_152490.3):c.824_825dupTT (p.(Ile276fs)), B3GALNT2(NM_152490.4):c.824_825dupTT (p.I276Lfs*26), B3GALNT2(NM_152490.5):c.824_825dupTT (p....) |
| ISCN |
- |
| DB-ID |
B3GALNT2_000008 See all 5 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 |
2024-04-19 20:20:39 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
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