MSH2 c.832del ;(p.E278Nfs*14)

Variant ID: 2-47641447-AG-A

NM_000251.2(MSH2):c.832del;(p.E278Nfs*14)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mutation spectrum and risk of colorectal cancer in African American families with Lynch syndrome.

Gastroenterology
Guindalini, Rodrigo Santa Cruz RS; Win, Aung Ko AK; Gulden, Cassandra C; Lindor, Noralane M NM; Newcomb, Polly A PA; Haile, Robert W RW; Raymond, Victoria V; Stoffel, Elena E; Hall, Michael M; Llor, Xavier X; Ukaegbu, Chinedu I CI; Solomon, Ilana I; Weitzel, Jeffrey J; Kalady, Matthew M; Blanco, Amie A; Terdiman, Jonathan J; Shuttlesworth, Gladis A GA; Lynch, Patrick M PM; Hampel, Heather H; Lynch, Henry T HT; Jenkins, Mark A MA; Olopade, Olufunmilayo I OI; Kupfer, Sonia S SS
Publication Date: 2015-11

Variant appearance in text: MSH2: 832delG
PubMed Link: 26248088
Variant Present in the following documents:
  • Main text
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