TTN c.34894_34895insG ;(p.L11632Rfs*4)

Variant ID: 2-179537169-A-AC

NM_001267550.1(TTN):c.34894_34895insG;(p.L11632Rfs*4)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project.

American Journal Of Human Genetics
Ceyhan-Birsoy, Ozge O; Murry, Jaclyn B JB; Machini, Kalotina K; Lebo, Matthew S MS; Yu, Timothy W TW; Fayer, Shawn S; Genetti, Casie A CA; Schwartz, Talia S TS; Agrawal, Pankaj B PB; Parad, Richard B RB; Holm, Ingrid A IA; McGuire, Amy L AL; Green, Robert C RC; Rehm, Heidi L HL; Beggs, Alan H AH; ,
Publication Date: 2019-01-03

Variant appearance in text: TTN: 34894_34895insG
PubMed Link: 30609409
Variant Present in the following documents:
  • Main text
View BVdb publication page