Variant #0001045664 (NC_000001.10:g.235634257_235634301del, NC_000001.10(NM_152490.3):c.652-26_670del (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.235634257_235634301del |
DNA change (hg38) |
- |
Published as |
B3GALNT2(NM_152490.5):c.652-26_670del |
ISCN |
- |
DB-ID |
TBCE_000115 |
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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2025-07-08 13:22:38 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
|