Variant #0000326726 (NC_000019.9:g.50169995G>A, NM_001571.5:c.-1116C>T (IRF3))

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.50169995G>A
DNA change (hg38) g.49666738G>A
Published as BCL2L12(NM_001040668.1):c.298G>A (p.(Val100Ile))
ISCN -
DB-ID BCL2L12_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L12 NM_001040668.1 ?/. - c.298G>A r.(?) p.(Val100Ile)
IRF3 NM_001571.5 ?/. - c.-1116C>T r.(?) p.(=)


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