Variant #0000858374 (NC_000002.11:g.220434993G>A, NM_015311.2:c.962C>T (OBSL1))
Chromosome |
2 |
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.220434993G>A |
DNA change (hg38) |
- |
Published as |
OBSL1(NM_001173408.1):c.962C>T (p.(Ala321Val)) |
ISCN |
- |
DB-ID |
INHA_000030 |
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) |
1.0E-5 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2022-05-09 15:51:19 +02:00 (CEST) |
Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
|