MSH6 c.3955A>C ;(p.K1319Q)

Variant ID: 2-48033744-A-C

NM_000179.2(MSH6):c.3955A>C;(p.K1319Q)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A molecular inversion probe-based next-generation sequencing panel to detect germline mutations in Chinese early-onset colorectal cancer patients.

Oncotarget
Zhang, Junxiao J; Wang, Xiaoyan X; de Voer, Richarda M RM; Hehir-Kwa, Jayne Y JY; Kamping, Eveline J EJ; Weren, Robbert D A RDA; Nelen, Marcel M; Hoischen, Alexander A; Ligtenberg, Marjolijn J L MJL; Hoogerbrugge, Nicoline N; Yang, Xiangling X; Yang, Zihuan Z; Fan, Xinjuan X; Wang, Lei L; Liu, Huanliang H; Wang, Jianping J; Kuiper, Roland P RP; van Kessel, Ad Geurts AG
Publication Date: 2017-04-11

Variant appearance in text: MSH6: 3955A>C; Lys1319Gln
PubMed Link: 28445943
Variant Present in the following documents:
  • Main text
  • oncotarget-08-24533.pdf
View BVdb publication page