RET c.1999_2001delinsTAT ;(p.P667Y)

Variant ID: 10-43610047-CCA-TAT

NM_020975.4(RET):c.1999_2001delinsTAT;(p.P667Y)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results.

Human Mutation
Plon, Sharon E SE; Eccles, Diana M DM; Easton, Douglas D; Foulkes, William D WD; Genuardi, Maurizio M; Greenblatt, Marc S MS; Hogervorst, Frans B L FB; Hoogerbrugge, Nicoline N; Spurdle, Amanda B AB; Tavtigian, Sean V SV; ,
Publication Date: 2008-11

Variant appearance in text: RET: P667Y
PubMed Link: 18951446
Variant Present in the following documents:
  • Main text
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