Variant #0000692863 (NC_000019.9:g.50163997C>T, NM_021228.2:c.*2341C>T (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.50163997C>T
DNA change (hg38) -
Published as IRF3(NM_001571.6):c.1071G>A (p.P357=)
ISCN -
DB-ID BCL2L12_000008
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
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.-5084C>T r.(?) p.(=)
IRF3 NM_001571.5 -?/. - c.1071G>A r.(?) p.(Pro357=)
SCAF1 NM_021228.2 -?/. - c.*2341C>T r.(=) p.(=)


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