MSH6 c.1490_1491insC ;(p.R497Sfs*10)

Variant ID: 2-48026612-G-GC

NM_000179.2(MSH6):c.1490_1491insC;(p.R497Sfs*10)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Hereditary non-polyposis colorectal cancer: clinical and molecular evidence for a new entity of hereditary colorectal cancer.

Gut
Mueller-Koch, Y Y; Vogelsang, H H; Kopp, R R; Lohse, P P; Keller, G G; Aust, D D; Muders, M M; Gross, M M; Daum, J J; Schiemann, U U; Grabowski, M M; Scholz, M M; Kerker, B B; Becker, I I; Henke, G G; Holinski-Feder, E E
Publication Date: 2005-12

Variant appearance in text: MSH6: 1490insC
PubMed Link: 15955785
Variant Present in the following documents:
  • Main text
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