Variant #0000552435 (NC_000014.8:g.24629498A>C, NM_017999.4:c.3047A>C (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.24629498A>C
DNA change (hg38) g.24160289A>C
Published as RNF31(NM_017999.5):c.3047A>C (p.D1016A)
ISCN -
DB-ID IRF9_000001
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IRF9 NM_006084.4 ?/. - c.-1051A>C r.(?) p.(=)
RNF31 NM_017999.4 ?/. - c.3047A>C r.(?) p.(Asp1016Ala)


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