Variant #0000300174 (NC_000001.10:g.247582464_247582466del, NLRP3(NM_004895.4):c.283+85_283+87del)

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.247582464_247582466del
DNA change (hg38) g.247419162_247419164del
Published as NLRP3(NM_001243133.1):c.277+85_277+87delATA
ISCN -
DB-ID NLRP3_000004
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Utrecht
Database submission license No license selected
Created by VKGL-NL_Utrecht
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NLRP3 NM_004895.4 -/. - c.283+85_283+87del r.(=) p.(=)