Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913273
rs121913273
0.010 GeneticVariation BEFREE A nonsense mutation in PTPN11 (K99X), a pathogenic CCND1 splice site variant (P241P), a hotspot missense mutation in PIK3CA (E542K) and a hotspot missense mutation in TP53 (R249S); were observed in 25%, 75%, 30% and 40% of the HER2+ BC tissue samples, respectively. 30535550

2019

dbSNP: rs1442481831
rs1442481831
0.010 GeneticVariation BEFREE Of these, two mutations, the somatic mutations <i>ERBB4</i>-V721I and <i>ERBB4</i>-S303F, were stably transfected into HCC1954 (PIK3CA mutant), HCC1569 (PIK3CA wildtype) and BT474 (PIK3CA mutant, ER positive) HER2+ breast cancer cell lines for functional <i>in vitro</i> experiments. 30023006

2018

dbSNP: rs121913279
rs121913279
0.010 GeneticVariation BEFREE In the present study, we generated a compound mouse model that genetically mimics HER2-positive breast cancer with coexisting PIK3CA(H1047R). 26640141

2016