Variant #0000566622 (NC_000019.9:g.18280085C>T, NM_005027.3:c.2168C>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.18280085C>T
DNA change (hg38) g.18169275C>T
Published as PIK3R2(NM_005027.3):c.2168C>T (p.P723L), PIK3R2(NM_005027.4):c.2168C>T (p.P723L)
ISCN -
DB-ID PIK3R2_000031 See all 2 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) 0.0003 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.2168C>T r.(?) p.(Pro723Leu)
IFI30 NM_006332.3 ?/. - c.-4567C>T r.(?) p.(=)


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