Variant #0000518540 (NC_000003.11:g.178957855G>C, NM_006218.2:c.*5703G>C (PIK3CA))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.178957855G>C
DNA change (hg38) g.179240067G>C
Published as KCNMB3(NM_001163677.1):c.454-3C>G (p.?)
ISCN -
DB-ID KCNMB3_000017
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNMB3 NM_001163677.1 ?/. - c.454-3C>G r.spl? p.?
PIK3CA NM_006218.2 ?/. - c.*5703G>C r.(=) p.(=)


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