Variant #0000518523 (NC_000003.11:g.178916941_178916943del, NM_006218.2:c.328_330del (PIK3CA))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.178916941_178916943del
DNA change (hg38) g.179199153_179199155del
Published as PIK3CA(NM_006218.4):c.328_330delGAA (p.E110del)
ISCN -
DB-ID KCNMB3_000005
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNMB3 NM_001163677.1 +?/. - c.*40844_*40846del r.(=) p.(=)
PIK3CA NM_006218.2 +?/. - c.328_330del r.(?) p.(Glu110del)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.