MSH6 c.3438+1G>C

Variant ID: 2-48030825-G-C

NM_000179.2(MSH6):c.3438+1G>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients.

Breast Cancer Research And Treatment
Crawford, Beth B; Adams, Sophie B SB; Sittler, Taylor T; van den Akker, Jeroen J; Chan, Salina S; Leitner, Ofri O; Ryan, Lauren L; Gil, Elad E; van 't Veer, Laura L
Publication Date: 2017-06

Variant appearance in text: MSH6: 3438+1G>C
PubMed Link: 28281021
Variant Present in the following documents:
  • Main text
View BVdb publication page