Variant #0000617803 (NC_000019.9:g.50169179C>G, NM_001571.5:c.-300G>C (IRF3))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50169179C>G
DNA change (hg38) g.49665922C>G
Published as BCL2L12(NM_138639.1):c.99C>G (p.P33=)
ISCN -
DB-ID BCL2L12_000005
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) 0.00014 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-16 10:47:28 +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.99C>G r.(?) p.(Pro33=)
IRF3 NM_001571.5 -?/. - c.-300G>C r.(?) p.(=)


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