Variant #0000349072 (NC_000017.10:g.19261246A>G, NM_015681.3:c.151T>C (B9D1))
| Chromosome |
17 |
| 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.19261246A>G |
| DNA change (hg38) |
g.19357933A>G |
| Published as |
B9D1(NM_001243473.1):c.210T>C (p.S70=), B9D1(NM_015681.3):c.151T>C (p.(Ser51Pro)) |
| ISCN |
- |
| DB-ID |
B9D1_000008 See all 4 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) |
4.0E-5 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-08-03 21:30:42 +02:00 (CEST) |

Variant on transcripts
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