TTN c.91661C>A ;(p.P30554Q)

Variant ID: 2-179414904-G-T

NM_001267550.1(TTN):c.91661C>A;(p.P30554Q)

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: TTN: 91661C>A; Pro30554Gln
PubMed Link: 35546177
Variant Present in the following documents:
  • 41598_2022_11932_MOESM1_ESM.xlsx, sheet 2
View BVdb publication page