TTN c.47077G>A ;(p.V15693I)

Variant ID: 2-179483108-C-T

NM_001267550.1(TTN):c.47077G>A;(p.V15693I)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genomic clonal evolution correlated with phenotype and prognosis in gastric cancer.

Clinical And Translational Medicine
Ge, Jie J; Li, Xuan X; Deng, Zhenghao Z; Gao, Xuan X; Liu, Yaoyao Y; Xiong, Xingui X; Zhao, Xianhui X; Peng, Huan H; Yi, Xin X; Xia, Xuefeng X; Chen, Zihua Z; Li, Lifeng L; Zhou, Haiyan H; Liu, Heli H
Publication Date: 2022-04

Variant appearance in text: TTN: 47077G>A; V15693I
PubMed Link: 35384329
Variant Present in the following documents:
  • CTM2-12-e799-s006.xlsx, sheet 2
View BVdb publication page



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: V15693I
PubMed Link: 30404001
Variant Present in the following documents:
  • NIHMS1512150-supplement-5.xlsx, sheet 1
View BVdb publication page