Variant #0000506771 (NC_000001.10:g.247582309C>T, NLRP3(NM_004895.4):c.213C>T)

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.247582309C>T
DNA change (hg38) g.247419007C>T
Published as NLRP3(NM_001079821.2):c.213C>T (p.(=)), NLRP3(NM_001243133.1):c.207C>T (p.A69=)
ISCN -
DB-ID NLRP3_000176 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) 0.00159 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NLRP3 NM_004895.4 -/. - c.213C>T r.(?) p.(Ala71=)