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