Variant #0000326347 (NC_000019.9:g.18286007C>T, NM_005027.3:c.*5903C>T (PIK3R2))

Chromosome 19
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.18286007C>T
DNA change (hg38) g.18175197C>T
Published as IFI30(NM_006332.3):c.290C>T (p.(Thr97Met))
ISCN -
DB-ID IFI30_000002
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 2018-01-15 20:58:59 +01:00 (CET)
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     
PIK3R2 NM_005027.3 ?/. - c.*5903C>T r.(=) p.(=)
IFI30 NM_006332.3 ?/. - c.290C>T r.(?) p.(Thr97Met)


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