TTN c.29416A>C ;(p.K9806Q)

Variant ID: 2-179571185-T-G

NM_001267550.1(TTN):c.29416A>C;(p.K9806Q)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Reliability of Whole-Exome Sequencing for Assessing Intratumor Genetic Heterogeneity.

Cell Reports
Shi, Weiwei W; Ng, Charlotte K Y CKY; Lim, Raymond S RS; Jiang, Tingting T; Kumar, Sushant S; Li, Xiaotong X; Wali, Vikram B VB; Piscuoglio, Salvatore S; Gerstein, Mark B MB; Chagpar, Anees B AB; Weigelt, Britta B; Pusztai, Lajos L; Reis-Filho, Jorge S JS; Hatzis, Christos C
Publication Date: 2018-11-06

Variant appearance in text: TTN: K9806Q
PubMed Link: 30404001
Variant Present in the following documents:
  • NIHMS1512150-supplement-4.xlsx, sheet 1
View BVdb publication page