Variant #0000518522 (NC_000003.11:g.178916931C>A, NM_006218.2:c.318C>A (PIK3CA))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.178916931C>A
DNA change (hg38) g.179199143C>A
Published as PIK3CA(NM_006218.2):c.318C>A (p.G106=)
ISCN -
DB-ID KCNMB3_000004 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) 0.00061 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 08:55:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNMB3 NM_001163677.1 -?/. - c.*40853G>T r.(=) p.(=)
PIK3CA NM_006218.2 -?/. - c.318C>A r.(?) p.(Gly106=)


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