Variant #0000724746 (NC_000014.8:g.24626618G>A, NC_000014.8(NM_017999.4):c.2608+5G>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.24626618G>A
DNA change (hg38) -
Published as RNF31(NM_017999.5):c.2608+5G>A
ISCN -
DB-ID IRF9_000008 See all 2 reported entries
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 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 2021-02-08 18:36:18 +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.-3931G>A r.(?) p.(=)
RNF31 NM_017999.4 ?/. - c.2608+5G>A r.spl? p.?


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