MSH2 c.757_759delinsTAT ;(p.M253Y)

Variant ID: 2-47639664-ATG-TAT

NM_000251.2(MSH2):c.757_759delinsTAT;(p.M253Y)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Predicting the impact of Lynch syndrome-causing missense mutations from structural calculations.

Plos Genetics
Nielsen, Sofie V SV; Stein, Amelie A; Dinitzen, Alexander B AB; Papaleo, Elena E; Tatham, Michael H MH; Poulsen, Esben G EG; Kassem, Maher M MM; Rasmussen, Lene J LJ; Lindorff-Larsen, Kresten K; Hartmann-Petersen, Rasmus R
Publication Date: 2017-04

Variant appearance in text: MSH2: M253Y
PubMed Link: 28422960
Variant Present in the following documents:
  • Main text
  • pgen.1006739.pdf
View BVdb publication page