Variant #0000327514 (NC_000002.11:g.171702088G>A, NM_000817.2:c.824G>A (GAD1))
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.171702088G>A |
DNA change (hg38) |
g.170845578G>A |
Published as |
GAD1(NM_000817.2):c.824G>A (p.(Gly275Asp)) |
ISCN |
- |
DB-ID |
GAD1_000003 |
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) |
Retrieve |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-08-06 14:59:34 +02:00 (CEST) |

Variant on transcripts
|