Variant #0000657428 (NC_000014.8:g.24631460C>G, NM_017999.4:c.*1678C>G (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.24631460C>G
DNA change (hg38) g.24162251C>G
Published as IRF9(NM_006084.4):c.107C>G (p.T36S)
ISCN -
DB-ID IRF9_000004
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +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.107C>G r.(?) p.(Thr36Ser)
RNF31 NM_017999.4 ?/. - c.*1678C>G r.(=) p.(=)


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