MSH2 c.763_766delinsTT ;(p.S255Ffs*28)

Variant ID: 2-47639670-AGTG-TT

NM_000251.2(MSH2):c.763_766delinsTT;(p.S255Ffs*28)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


HNPCC: six new pathogenic mutations.

Bmc Medical Genetics
Kunstmann, Erdmute E; Vieland, Judith J; Brasch, Frank E FE; Hahn, Stephan A SA; Epplen, Joerg T JT; Schulmann, Karsten K; Schmiegel, Wolff W
Publication Date: 2004-06-24

Variant appearance in text: MSH2: 763_766delAGTGinsTT
PubMed Link: 15217520
Variant Present in the following documents:
  • Main text
  • 1471-2350-5-16.pdf
View BVdb publication page