Variant #0000658633 (NC_000019.9:g.50162875G>A, NM_021228.2:c.*1219G>A (SCAF1))

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.50162875G>A
DNA change (hg38) g.49659618G>A
Published as IRF3(NM_001197122.2):c.1330C>T (p.P444S)
ISCN -
DB-ID BCL2L12_000007
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 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.-6206G>A r.(?) p.(=)
IRF3 NM_001571.5 -?/. - c.*30C>T r.(=) p.(=)
SCAF1 NM_021228.2 -?/. - c.*1219G>A r.(=) p.(=)


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