MSH6 c.1636G>T ;(p.E546*)

Variant ID: 2-48026758-G-T

NM_000179.2(MSH6):c.1636G>T;(p.E546*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Frequency of mutations in mismatch repair genes in a population-based study of women with ovarian cancer.

British Journal Of Cancer
Pal, T T; Akbari, M R MR; Sun, P P; Lee, J-H JH; Fulp, J J; Thompson, Z Z; Coppola, D D; Nicosia, S S; Sellers, T A TA; McLaughlin, J J; Risch, H A HA; Rosen, B B; Shaw, P P; Schildkraut, J J; Narod, S A SA
Publication Date: 2012-11-06

Variant appearance in text: MSH6: Glu546X
PubMed Link: 23047549
Variant Present in the following documents:
  • Main text
  • bjc2012452a.pdf
View BVdb publication page