Variant #0000947190 (NC_000001.10:g.247587643C>T, NM_004895.4:c.898C>T (NLRP3))

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.247587643C>T
DNA change (hg38) -
Published as NLRP3(NM_004895.5):c.898C>T (p.L300F)
ISCN -
DB-ID NLRP3_000264
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +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.892C>T r.(?) p.(Leu298Phe)
NLRP3 NM_004895.4 ?/. - c.898C>T r.(?) p.(Leu300Phe)


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