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MSH6 c.1635A>C ;(p.K545N)
Variant ID: 2-48026757-A-C
NM_000179.2(
MSH6
):c.1635A>C;(p.K545N)
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:
Comprehensive germline and somatic genomic profiles of Chinese patients with biliary tract cancer.
Frontiers In Oncology
Yu, Haipeng H; Xu, Yan Y; Gao, Wei W; Li, Mei M; He, Ji'an J; Deng, Xiaoqian X; Xing, Wenge W
Publication Date: 2022
Variant appearance in text: MSH6: K545N
PubMed Link:
36072793
Variant Present in the following documents:
Table_3.xlsx, sheet 1
View BVdb publication page
Clinical Utility of Targeted Sequencing in Lung Cancer: Experience From an Autonomous Swedish Health Care Center.
Jto Clinical And Research Reports
Isaksson, Sofi S; Hazem, Bassam B; Jönsson, Mats M; Reuterswärd, Christel C; Karlsson, Anna A; Griph, Håkan H; Engleson, Jens J; Oskarsdottir, Gudrun G; Öhman, Ronny R; Holm, Karolina K; Rosengren, Frida F; Annersten, Karin K; Jönsson, Göran G; Borg, Åke Å; Edsjö, Anders A; Levéen, Per P; Brunnström, Hans H; Lindquist, Kajsa Ericson KE; Staaf, Johan J; Planck, Maria M
Publication Date: 2020-03
Variant appearance in text: MSH6: Lys545Asn
PubMed Link:
34589915
Variant Present in the following documents:
main.pdf
View BVdb publication page