Variant #0000911027 (NC_000001.10:g.247587424G>A, NM_004895.4:c.679G>A (NLRP3))

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.247587424G>A
DNA change (hg38) -
Published as NLRP3(NM_004895.4):c.679G>A (p.A227T)
ISCN -
DB-ID NLRP3_000259
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 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NLRP3 NM_001243133.1 -?/. - c.673G>A r.(?) p.(Ala225Thr)
NLRP3 NM_004895.4 -?/. - c.679G>A r.(?) p.(Ala227Thr)


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