Variant #0000518525 (NC_000003.11:g.178917595A>G, NM_006218.2:c.470A>G (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.178917595A>G
DNA change (hg38) g.179199807A>G
Published as PIK3CA(NM_006218.2):c.470A>G (p.N157S)
ISCN -
DB-ID KCNMB3_000006 See all 3 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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.*40189T>C r.(=) p.(=)
PIK3CA NM_006218.2 -?/. - c.470A>G r.(?) p.(Asn157Ser)


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