MSH6 c.628_630delinsTTT ;(p.V210F)

Variant ID: 2-48025750-GTA-TTT

NM_000179.2(MSH6):c.628_630delinsTTT;(p.V210F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID.

Plos One
Offer, Steven M SM; Pan-Hammarström, Qiang Q; Hammarström, Lennart L; Harris, Reuben S RS
Publication Date: 2010-08-18

Variant appearance in text: MSH6: V210F
PubMed Link: 20805886
Variant Present in the following documents:
  • Main text
View BVdb publication page