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
|