ERBB2 c.1431del ;(p.H478Tfs*78)

Variant ID: 17-37872110-TG-T

NM_004448.2(ERBB2):c.1431del;(p.H478Tfs*78)

This variant was identified in 1 publication

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: 1431del
PubMed Link: 34113003
Variant Present in the following documents:
  • 41436_2021_Article_1234.pdf
View BVdb publication page