Variant #0000571850 (NC_000022.10:g.34046370C>T, NM_004737.4:c.391G>A (LARGE))
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.34046370C>T |
DNA change (hg38) |
g.33650384C>T |
Published as |
LARGE(NM_004737.4):c.391G>A (p.(Val131Ile)), LARGE1(NM_004737.6):c.391G>A (p.V131I), LARGE1(NM_004737.7):c.391G>A (p.V131I) |
ISCN |
- |
DB-ID |
LARGE_000069 See all 3 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) |
0.00056 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
|