Variant #0000506001 (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) |
g.235465654_235465655dup |
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 |
TBCE_000059 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_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
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