Variant #0000895088 (NC_000019.9:g.50162920G>A, NM_021228.2:c.*1264G>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.50162920G>A
DNA change (hg38) -
Published as IRF3(NM_001571.6):c.1269C>T (p.G423=)
ISCN -
DB-ID BCL2L12_000014
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) 1.0E-5 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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L12 NM_001040668.1 -?/. - c.-6161G>A r.(?) p.(=)
IRF3 NM_001571.5 -?/. - c.1269C>T r.(?) p.(Gly423=)
SCAF1 NM_021228.2 -?/. - c.*1264G>A r.(=) p.(=)


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