Variant #0000617468 (NC_000019.9:g.18280044C>T, NM_005027.3:c.2127C>T (PIK3R2))

Chromosome 19
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.18280044C>T
DNA change (hg38) g.18169234C>T
Published as PIK3R2(NM_005027.2):c.2127C>T (p.(Thr709=)), PIK3R2(NM_005027.3):c.2127C>T (p.T709=), PIK3R2(NM_005027.4):c.2127C>T (p.T709=)
ISCN -
DB-ID PIK3R2_000022 See all 4 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) 0.04937 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +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.2127C>T r.(?) p.(Thr709=)
IFI30 NM_006332.3 -?/. - c.-4608C>T r.(?) p.(=)


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