MSH2 c.377del ;(p.G126Afs*48)

Variant ID: 2-47637241-TG-T

NM_000251.2(MSH2):c.377del;(p.G126Afs*48)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Implication of DNA repair genes in Lynch-like syndrome.

Familial Cancer
Xicola, Rosa M RM; Clark, Julia R JR; Carroll, Timothy T; Alvikas, Jurgis J; Marwaha, Priti P; Regan, Maureen R MR; Lopez-Giraldez, Francesc F; Choi, Jungmin J; Emmadi, Rajyasree R; Alagiozian-Angelova, Victoria V; Kupfer, Sonia S SS; Ellis, Nathan A NA; Llor, Xavier X
Publication Date: 2019-07

Variant appearance in text: MSH2: 376delG
PubMed Link: 30989425
Variant Present in the following documents:
  • Main text
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