ERBB2 c.196C>T ;(p.P66S)

Variant ID: 17-37863365-C-T

NM_004448.2(ERBB2):c.196C>T;(p.P66S)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Clinical utility of testing for PALB2 and CHEK2 c.1100delC in breast and ovarian cancer.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Woodward, Emma R ER; van Veen, Elke M EM; Forde, Claire C; Harkness, Elaine F EF; Byers, Helen J HJ; Ellingford, Jamie M JM; Burghel, George J GJ; Schlech, Helene H; Bowers, Naomi L NL; Wallace, Andrew J AJ; Howell, Sacha J SJ; Howell, Anthony A; Lalloo, Fiona F; Newman, William G WG; Smith, Miriam J MJ; Gareth Evans, D D
Publication Date: 2021-10

Variant appearance in text: HER2: 196C>T
PubMed Link: 34113003
Variant Present in the following documents:
  • 41436_2021_Article_1234.pdf
View BVdb publication page



Dual-molecular barcode sequencing detects rare variants in tumor and cell free DNA in plasma.

Scientific Reports
Hirotsu, Yosuke Y; Otake, Sotaro S; Ohyama, Hiroshi H; Amemiya, Kenji K; Higuchi, Rumi R; Oyama, Toshio T; Mochizuki, Hitoshi H; Goto, Taichiro T; Omata, Masao M
Publication Date: 2020-02-25

Variant appearance in text: ERBB2: 196C>T
PubMed Link: 32099048
Variant Present in the following documents:
  • 41598_2020_Article_60361.pdf
View BVdb publication page