MSH6 c.4035del ;(p.D1346Mfs*9)

Variant ID: 2-48033951-TA-T

NM_000179.2(MSH6):c.4035del;(p.D1346Mfs*9)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update.

European Journal Of Human Genetics : Ejhg
McGuigan, Anthony A; Whitworth, James J; Andreou, Avgi A; Hearn, Timothy T; , ; Tischkowitz, Marc M; Maher, Eamonn R ER
Publication Date: 2022-03

Variant appearance in text: MSH6: 4035delA
PubMed Link: 34983940
Variant Present in the following documents:
  • 41431_2021_1013_MOESM1_ESM.pdf
View BVdb publication page