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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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; LubiĆski, 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