MSH6 c.206_207delinsAC ;(p.A69D)

Variant ID: 2-48010578-CG-AC

NM_000179.2(MSH6):c.206_207delinsAC;(p.A69D)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Prevalence of pathogenic germline cancer risk variants in high-risk urothelial carcinoma.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Nassar, Amin H AH; Abou Alaiwi, Sarah S; AlDubayan, Saud H SH; Moore, Nicholas N; Mouw, Kent W KW; Kwiatkowski, David J DJ; Choueiri, Toni K TK; Curran, Catherine C; Berchuck, Jacob E JE; Harshman, Lauren C LC; Nuzzo, Pier V PV; Chanza, Nieves Martinez NM; Van Allen, Eliezer E; Esplin, Edward D ED; Yang, Shan S; Callis, Thomas T; Garber, Judy E JE; Rana, Huma Q HQ; Sonpavde, Guru G
Publication Date: 2020-04

Variant appearance in text: MSH6: A69D
PubMed Link: 31844177
Variant Present in the following documents:
  • Main text
View BVdb publication page