MSH6 c.1516G>A ;(p.D506N)

Variant ID: 2-48026638-G-A

NM_000179.2(MSH6):c.1516G>A;(p.D506N)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Distinctive DNA mismatch repair and APC rare variants in African Americans with colorectal neoplasia.

Oncotarget
Ashktorab, Hassan H; Azimi, Hamed H; Varma, Sudhir S; Tavakoli, Payaam P; Nickerson, Michael L ML; Brim, Hassan H
Publication Date: 2017-11-21

Variant appearance in text: MSH6: D506N
PubMed Link: 29245953
Variant Present in the following documents:
  • oncotarget-08-99966-s003.xlsx, sheet 2
View BVdb publication page



DNA replication fidelity and cancer.

Seminars In Cancer Biology
Preston, Bradley D BD; Albertson, Tina M TM; Herr, Alan J AJ
Publication Date: 2010-10

Variant appearance in text: MSH6: D506N
PubMed Link: 20951805
Variant Present in the following documents:
  • Main text
View BVdb publication page