KCNQ1 c.1858_1859delinsGC ;(p.H620A)

Variant ID: 11-2869060-CA-GC

NM_000218.2(KCNQ1):c.1858_1859delinsGC;(p.H620A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Two missense mutations in KCNQ1 cause pituitary hormone deficiency and maternally inherited gingival fibromatosis.

Nature Communications
Tommiska, Johanna J; Känsäkoski, Johanna J; Skibsbye, Lasse L; Vaaralahti, Kirsi K; Liu, Xiaonan X; Lodge, Emily J EJ; Tang, Chuyi C; Yuan, Lei L; Fagerholm, Rainer R; Kanters, Jørgen K JK; Lahermo, Päivi P; Kaunisto, Mari M; Keski-Filppula, Riikka R; Vuoristo, Sanna S; Pulli, Kristiina K; Ebeling, Tapani T; Valanne, Leena L; Sankila, Eeva-Marja EM; Kivirikko, Sirpa S; Lääperi, Mitja M; Casoni, Filippo F; Giacobini, Paolo P; Phan-Hug, Franziska F; Buki, Tal T; Tena-Sempere, Manuel M; Pitteloud, Nelly N; Veijola, Riitta R; Lipsanen-Nyman, Marita M; Kaunisto, Kari K; Mollard, Patrice P; Andoniadou, Cynthia L CL; Hirsch, Joel A JA; Varjosalo, Markku M; Jespersen, Thomas T; Raivio, Taneli T
Publication Date: 2017-11-03

Variant appearance in text: KCNQ1: H620A
PubMed Link: 29097701
Variant Present in the following documents:
  • Main text
  • 41467_2017_Article_1429.pdf
  • 41467_2017_1429_MOESM1_ESM.pdf
View BVdb publication page