Variant #0000914182 (NC_000014.8:g.24632737C>G, NM_017999.4:c.*2955C>G (RNF31))

Chromosome 14
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.24632737C>G
DNA change (hg38) -
Published as IRF9(NM_006084.5):c.495+20C>G
ISCN -
DB-ID IRF9_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) 0.00053 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 2023-01-11 15:44:22 +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     
IRF9 NM_006084.4 -?/. - c.495+20C>G r.(=) p.(=)
RNF31 NM_017999.4 -?/. - c.*2955C>G r.(=) p.(=)


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