Variant #0000506781 (NC_000001.10:g.247587259C>T, NLRP3(NM_004895.4):c.514C>T)

Chromosome 1
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.247587259C>T
DNA change (hg38) g.247423957C>T
Published as NLRP3(NM_001243133.1):c.508C>T (p.R170C)
ISCN -
DB-ID NLRP3_000182
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NLRP3 NM_001243133.1 ?/. - c.508C>T r.(?) p.(Arg170Cys)
NLRP3 NM_004895.4 ?/. - c.514C>T r.(?) p.(Arg172Cys)