Variant #0000293767 (NC_000019.9:g.18280096G>A, NM_005027.3:c.2179G>A (PIK3R2))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.18280096G>A
DNA change (hg38) g.18169286G>A
Published as PIK3R2(NM_005027.2):c.2179G>A (p.(Ala727Thr)), PIK3R2(NM_005027.3):c.2179G>A (p.A727T), PIK3R2(NM_005027.4):c.2179G>A (p.A727T)
ISCN -
DB-ID PIK3R2_000024 See all 3 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) 0.04161 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.2179G>A r.(?) p.(Ala727Thr)
IFI30 NM_006332.3 -/. - c.-4556G>A r.(?) p.(=)


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