PIK3CA c.1004G>A ;(p.R335K)

Variant ID: 3-178921522-G-A

NM_006218.2(PIK3CA):c.1004G>A;(p.R335K)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Development and validation of a whole-exome sequencing test for simultaneous detection of point mutations, indels and copy-number alterations for precision cancer care.

Npj Genomic Medicine
Rennert, Hanna H; Eng, Kenneth K; Zhang, Tuo T; Tan, Adrian A; Xiang, Jenny J; Romanel, Alessandro A; Kim, Robert R; Tam, Wayne W; Liu, Yen-Chun YC; Bhinder, Bhavneet B; Cyrta, Joanna J; Beltran, Himisha H; Robinson, Brian B; Mosquera, Juan Miguel JM; Fernandes, Helen H; Demichelis, Francesca F; Sboner, Andrea A; Kluk, Michael M; Rubin, Mark A MA; Elemento, Olivier O
Publication Date: 2016

Variant appearance in text: PIK3CA: R335K
PubMed Link: 28781886
Variant Present in the following documents:
  • npjgenmed201619-s3.pdf
View BVdb publication page



Exome sequencing identifies early gastric carcinoma as an early stage of advanced gastric cancer.

Plos One
Kang, Guhyun G; Hwang, Woo Cheol WC; Do, In-Gu IG; Wang, Kai K; Kang, So Young SY; Lee, Jeeyun J; Park, Se Hoon SH; Park, Joon Oh JO; Kang, Won Ki WK; Jang, Jiryeon J; Choi, Min-Gew MG; Lee, Jun Ho JH; Sohn, Tae Sung TS; Bae, Jae Moon JM; Kim, Sung S; Kim, Min Ji MJ; Kim, Seonwoo S; Park, Cheol Keun CK; Kim, Kyoung-Mee KM
Publication Date: 2013

Variant appearance in text: PIK3CA: 1004G>A
PubMed Link: 24376576
Variant Present in the following documents:
  • pone.0082770.s002.xls, sheet 1
View BVdb publication page