Variant #0000518518 (NC_000003.11:g.178916519T>C, NC_000003.11(NM_006218.2):c.-76-19T>C (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.178916519T>C
DNA change (hg38) g.179198731T>C
Published as PIK3CA(NM_006218.2):c.-76-19T>C
ISCN -
DB-ID KCNMB3_000001
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_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 2020-03-23 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.*41265A>G r.(=) p.(=)
PIK3CA NM_006218.2 -?/. - c.-76-19T>C r.(=) p.(=)


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