KIT c.1195G>C ;(p.V399L)

Variant ID: 4-55575669-G-C

NM_000222.2(KIT):c.1195G>C;(p.V399L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Somatic mutations of KIT in familial testicular germ cell tumours.

British Journal Of Cancer
Rapley, E A EA; Hockley, S S; Warren, W W; Johnson, L L; Huddart, R R; Crockford, G G; Forman, D D; Leahy, M G MG; Oliver, D T DT; Tucker, K K; Friedlander, M M; Phillips, K-A KA; Hogg, D D; Jewett, M A S MA; Lohynska, R R; Daugaard, G G; Richard, S S; Heidenreich, A A; Geczi, L L; Bodrogi, I I; Olah, E E; Ormiston, W J WJ; Daly, P A PA; Looijenga, L H J LH; Guilford, P P; Aass, N N; Fosså, S D SD; Heimdal, K K; Tjulandin, S A SA; Liubchenko, L L; Stoll, H H; Weber, W W; Einhorn, L L; Weber, B L BL; McMaster, M M; Greene, M H MH; Bishop, D T DT; Easton, D D; Stratton, M R MR
Publication Date: 2004-06-14

Variant appearance in text: KIT: V399L
PubMed Link: 15150569
Variant Present in the following documents:
  • Main text
  • 90-6601880a.pdf
View BVdb publication page