MSH6 c.399_402del ;(p.F133Lfs*15)

Variant ID: 2-48018201-GTTTT-G

NM_000179.2(MSH6):c.399_402del;(p.F133Lfs*15)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Prevalence and spectrum of germline cancer susceptibility gene variants and somatic second hits in colorectal cancer.

American Journal Of Cancer Research
Liao, Haiyan H; Cai, Songhua S; Bai, Yuezong Y; Zhang, Bei B; Sheng, Yuling Y; Tong, Shuang S; Cai, Jinping J; Zhao, Feilong F; Zhao, Xiaochen X; Chen, Shiqing S; Zhang, Cheng C; Gao, Jing J
Publication Date: 2021

Variant appearance in text: MSH6: 399_402del
PubMed Link: 34873480
Variant Present in the following documents:
  • Main text
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