MSH2 c.1086_1144del ;(p.V363Sfs*6)

Variant ID: 2-47656890-TAGTGGAAGCTTTTGTAGAAGATGCAGAATTGAGGCAGACTTTACAAGAAGATTTACTTC-T

NM_000251.2(MSH2):c.1086_1144del;(p.V363Sfs*6)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations.

Gastroenterology
Haraldsdottir, Sigurdis S; Hampel, Heather H; Tomsic, Jerneja J; Frankel, Wendy L WL; Pearlman, Rachel R; de la Chapelle, Albert A; Pritchard, Colin C CC
Publication Date: 2014-12

Variant appearance in text: MSH2: 1086_1151del
PubMed Link: 25194673
Variant Present in the following documents:
  • Main text
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