PTEN c.571_572delinsTC ;(p.V191S)

Variant ID: 10-89711953-GT-TC

NM_000314.4(PTEN):c.571_572delinsTC;(p.V191S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Esophageal cancer in a family with hamartomatous tumors and germline PTEN frameshift and SMAD7 missense mutations.

Cancer Genetics
Sherman, Scott K SK; Maxwell, Jessica E JE; Qian, Qining Q; Bellizzi, Andrew M AM; Braun, Terry A TA; Iannettoni, Mark D MD; Darbro, Benjamin W BW; Howe, James R JR
Publication Date: 2015

Variant appearance in text: PTEN: V191S
PubMed Link: 25554686
Variant Present in the following documents:
  • Main text
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