Variant #0001039930 (NC_000014.8:g.24631432G>A, NM_017999.4:c.*1650G>A (RNF31))

Chromosome 14
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.24631432G>A
DNA change (hg38) -
Published as IRF9(NM_006084.5):c.79G>A (p.(Gly27Arg))
ISCN -
DB-ID IRF9_000020
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
IRF9 NM_006084.4 ?/. - c.79G>A r.(?) p.(Gly27Arg)
RNF31 NM_017999.4 ?/. - c.*1650G>A r.(=) p.(=)


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