Variant #0001044739 (NC_000003.11:g.178952085A>G, NM_006218.2:c.3140A>G (PIK3CA))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.178952085A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID PIK3CA_000002 See all 21 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs121913279
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-05-16 11:46:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIK3CA NM_006218.2 +/. - c.3140A>G r.(?) p.(His1047Arg)


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