Variant #0000855665 (NC_000019.9:g.50165494G>C, NM_021228.2:c.*3838G>C (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.50165494G>C
DNA change (hg38) -
Published as IRF3(NM_001571.6):c.693C>G (p.S231=)
ISCN -
DB-ID BCL2L12_000012
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:47:41 +02:00 (CEST)
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.-3587G>C r.(?) p.(=)
IRF3 NM_001571.5 -?/. - c.693C>G r.(?) p.(Ser231=)
SCAF1 NM_021228.2 -?/. - c.*3838G>C r.(=) p.(=)


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