KMT2C c.4602G>T ;(p.Q1534H)

Variant ID: 7-151891152-C-A

NM_170606.2(KMT2C):c.4602G>T;(p.Q1534H)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Parental segregation study reveals rare benign and likely benign variants in a Brazilian cohort of rare diseases.

Scientific Reports
Quaio, Caio Robledo D 'Angioli Costa CRD'C; Ceroni, Jose Ricardo Magliocco JRM; Cervato, Murilo Castro MC; Thurow, Helena Strelow HS; Moreira, Caroline Monaco CM; Trindade, Ana Carolina Gomes ACG; Furuzawa, Cintia Reys CR; de Souza, Rafaela Rogerio Floriano RRF; Perazzio, Sandro Felix SF; Dutra, Aurelio Pimenta AP; Chung, Christine Hsiaoyun CH; Kim, Chong Ae CA
Publication Date: 2022-05-11

Variant appearance in text: KMT2C: 4602G>T; Gln1534His; rs992987667
PubMed Link: 35546177
Variant Present in the following documents:
  • 41598_2022_11932_MOESM1_ESM.xlsx, sheet 2
View BVdb publication page