Variant #0001043106 (NC_000019.9:g.50162988G>C, NM_021228.2:c.*1332G>C (SCAF1))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.50162988G>C
DNA change (hg38) -
Published as IRF3(NM_001571.6):c.1201C>G (p.L401V)
ISCN -
DB-ID BCL2L12_000019
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L12 NM_001040668.1 ?/. - c.-6093G>C r.(?) p.(=)
IRF3 NM_001571.5 ?/. - c.1201C>G r.(?) p.(Leu401Val)
SCAF1 NM_021228.2 ?/. - c.*1332G>C r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.