Variant #0000505988 (NC_000001.10:g.235596323C>T, NM_152490.3:c.*17198G>A (B3GALNT2))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.235596323C>T |
| DNA change (hg38) |
g.235433008C>T |
| Published as |
TBCE(NM_001079515.2):c.661-1196C>T, TBCE(NM_001287801.2):c.723C>T (p.F241=) |
| ISCN |
- |
| DB-ID |
TBCE_000051 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_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2019-12-04 14:54:23 +01:00 (CET) |

Variant on transcripts
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