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 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NLRP3 NM_001243133.1 -?/. - c.592G>A r.(?) p.(Val198Met)
NLRP3 NM_004895.4 -?/. - c.598G>A r.(?) p.(Val200Met)