Variant #0000506783 (NC_000001.10:g.247587343G>A, NLRP3(NM_004895.4):c.598G>A)
Chromosome |
1 |
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.247587343G>A |
DNA change (hg38) |
g.247424041G>A |
Published as |
NLRP3(NM_001079821.2):c.598G>A (p.(Val200Met)), NLRP3(NM_001243133.1):c.592G>A (p.V198M), NLRP3(NM_001243133.2):c.592G>A (p.V198M) |
ISCN |
- |
DB-ID |
NLRP3_000184 See all 8 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) |
0.00849 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-07-07 10:10:56 +02:00 (CEST) |

Variant on transcripts
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