Variant #0000801148 (NC_000003.11:g.30686292C>G, NM_003242.5:c.148C>G (TGFBR2))
| Chromosome |
3 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.30686292C>G |
| DNA change (hg38) |
- |
| Published as |
TGFBR2(NM_001024847.2):c.223C>G (p.L75V) |
| ISCN |
- |
| DB-ID |
TGFBR2_000097 |
| 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_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
|