Variant #0000285254 (NC_000011.9:g.112025712G>A, NM_001562.2:c.65C>T (IL18))

Chromosome 11
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.112025712G>A
DNA change (hg38) g.112154989G>A
Published as IL18(NM_001562.4):c.65C>T (p.T22M)
ISCN -
DB-ID IL18_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) 0.00053 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL18 NM_001562.2 ?/. - c.65C>T r.(?) p.(Thr22Met)
TEX12 NM_031275.4 ?/. - c.-12515G>A r.(?) p.(=)


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