Variant #0000848258 (NC_000001.10:g.119683231A>C, NM_015836.3:c.37T>G (WARS2))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.119683231A>C |
DNA change (hg38) |
- |
Published as |
WARS2(NM_015836.4):c.37T>G (p.(Trp13Gly), p.W13G), WARS2(NM_201263.2):c.37T>G (p.W13G) |
ISCN |
- |
DB-ID |
WARS2_000007 See all 15 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) |
0.00322 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2022-05-09 15:40:45 +02:00 (CEST) |
Date last edited |
2024-04-19 20:20:39 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|