TTN c.29621_29624del ;(p.E9874Gfs*28)

Variant ID: 2-179569673-CCTCT-C

NM_001267550.1(TTN):c.29621_29624del;(p.E9874Gfs*28)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Targeted Sequencing of 242 Clinically Important Genes in the Russian Population From the Ivanovo Region.

Frontiers In Genetics
Ramensky, Vasily E VE; Ershova, Alexandra I AI; Zaicenoka, Marija M; Kiseleva, Anna V AV; Zharikova, Anastasia A AA; Vyatkin, Yuri V YV; Sotnikova, Evgeniia A EA; Efimova, Irina A IA; Divashuk, Mikhail G MG; Kurilova, Olga V OV; Skirko, Olga P OP; Muromtseva, Galina A GA; Belova, Olga A OA; Rachkova, Svetlana A SA; Pokrovskaya, Maria S MS; Shalnova, Svetlana A SA; Meshkov, Alexey N AN; Drapkina, Oxana M OM
Publication Date: 2021

Variant appearance in text: TTN: 29621_29624del
PubMed Link: 34691145
Variant Present in the following documents:
  • Data_Sheet_2.xlsx, sheet 3
View BVdb publication page



Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Töpf, Ana A; Johnson, Katherine K; Bates, Adam A; Phillips, Lauren L; Chao, Katherine R KR; England, Eleina M EM; Laricchia, Kristen M KM; Mullen, Thomas T; Valkanas, Elise E; Xu, Liwen L; Bertoli, Marta M; Blain, Alison A; Casasús, Ana B AB; Duff, Jennifer J; Mroczek, Magdalena M; Specht, Sabine S; Lek, Monkol M; Ensini, Monica M; MacArthur, Daniel G DG; , ; Straub, Volker V
Publication Date: 2020-09

Variant appearance in text: TTN: 29621_29624del; E9874Gfs*28
PubMed Link: 32528171
Variant Present in the following documents:
  • 41436_2020_840_MOESM10_ESM.xlsx, sheet 1
View BVdb publication page