Variant #0001005155 (NC_000019.9:g.56373460_56373461del, NM_145007.3:c.-26039_-26038del (NLRP11))

Chromosome 19
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.56373460_56373461del
DNA change (hg38) -
Published as NLRP4(NM_134444.4):c.2121_2122delTC (p.(Arg708fs))
ISCN -
DB-ID NLRP4_000006
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NLRP4 NM_134444.4 ?/. - c.2121_2122del r.(?) p.(Arg708*)
NLRP11 NM_145007.3 ?/. - c.-26039_-26038del r.(?) p.(=)


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