ERBB2 c.3398G>A ;(p.C1133Y)

Variant ID: 17-37883786-G-A

NM_004448.2(ERBB2):c.3398G>A;(p.C1133Y)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria.

American Journal Of Human Genetics
Pejaver, Vikas V; Byrne, Alicia B AB; Feng, Bing-Jian BJ; Pagel, Kymberleigh A KA; Mooney, Sean D SD; Karchin, Rachel R; O'Donnell-Luria, Anne A; Harrison, Steven M SM; Tavtigian, Sean V SV; Greenblatt, Marc S MS; Biesecker, Leslie G LG; Radivojac, Predrag P; Brenner, Steven E SE; ,
Publication Date: 2022-12-01

Variant appearance in text: ERBB2: C1133Y; rs1371638608
PubMed Link: 36413997
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page



Mutational drivers of cancer cell migration and invasion.

British Journal Of Cancer
Novikov, Nikita M NM; Zolotaryova, Sofia Y SY; Gautreau, Alexis M AM; Denisov, Evgeny V EV
Publication Date: 2021-01

Variant appearance in text: HER2: C1133Y
PubMed Link: 33204027
Variant Present in the following documents:
  • 41416_2020_Article_1149.pdf
View BVdb publication page