Variant #0001048379 (NC_000019.9:g.18273263C>G, NM_005027.3:c.1056C>G (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.18273263C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID PIK3R2_000056
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1568636630
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-09-25 11:43:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIK3R2 NM_005027.3 ?/. - c.1056C>G r.(?) p.(Phe352Leu)


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