MSH6 c.3172+20T>C

Variant ID: 2-48028314-T-C

NM_000179.2(MSH6):c.3172+20T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Prevalence and spectrum of MLH1, MSH2, and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients.

Hereditary Cancer In Clinical Practice
Rashid, Muhammad Usman MU; Naeemi, Humaira H; Muhammad, Noor N; Loya, Asif A; LubiƄski, Jan J; Jakubowska, Anna A; Yusuf, Muhammed Aasim MA
Publication Date: 2019

Variant appearance in text: rs3136335
PubMed Link: 31660093
Variant Present in the following documents:
  • Main text
  • 13053_2019_Article_128.pdf
View BVdb publication page



Targeted exome sequencing reveals distinct pathogenic variants in Iranians with colorectal cancer.

Oncotarget
Ashktorab, Hassan H; Mokarram, Pooneh P; Azimi, Hamed H; Olumi, Hasti H; Varma, Sudhir S; Nickerson, Michael L ML; Brim, Hassan H
Publication Date: 2017-01-31

Variant appearance in text: rs3136335
PubMed Link: 28002797
Variant Present in the following documents:
  • oncotarget-08-7852-s002.xlsx, sheet 13
View BVdb publication page