Variant #0000246186 (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) g.179234297A>G
Published as PIK3CA(NM_006218.4):c.3140A>G (p.H1047R)
ISCN -
DB-ID PIK3CA_000002 See all 21 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 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNMB3 NM_001163677.1 +/. - c.*5699T>C r.(=) p.(=)
PIK3CA NM_006218.2 +/. - c.3140A>G r.(?) p.(His1047Arg)


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