MSH2 c.445_446delinsAC ;(p.G149T)

Variant ID: 2-47637311-GG-AC

NM_000251.2(MSH2):c.445_446delinsAC;(p.G149T)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: MSH2: G149T
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer.

European Journal Of Human Genetics : Ejhg
Siltanen, Sanna S; Syrjäkoski, Kirsi K; Fagerholm, Rainer R; Ikonen, Tarja T; Lipman, Peter P; Mallott, Jacob J; Holli, Kaija K; Tammela, Teuvo L J TL; Järvinen, Heikki J HJ; Mecklin, Jukka-Pekka JP; Aittomäki, Kristiina K; Blomqvist, Carl C; Bailey-Wilson, Joan E JE; Nevanlinna, Heli H; Aaltonen, Lauri A LA; Schleutker, Johanna J; Vahteristo, Pia P
Publication Date: 2008-08

Variant appearance in text: MSH2: G149T
PubMed Link: 18337727
Variant Present in the following documents:
  • Main text
View BVdb publication page