TTN c.37879del ;(p.E12627Kfs*320)

Variant ID: 2-179522489-TC-T

NM_001267550.1(TTN):c.37879del;(p.E12627Kfs*320)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies.

Journal Of Translational Medicine
Lu, Chaoxia C; Wu, Wei W; Liu, Fang F; Yang, Kunqi K; Li, Jiacheng J; Liu, Yaping Y; Wang, Rongrong R; Si, Nuo N; Gao, Peng P; Liu, Yongtai Y; Zhang, Shuyang S; Zhang, Xue X
Publication Date: 2018-08-30

Variant appearance in text: TTN: 37879delG
PubMed Link: 30165862
Variant Present in the following documents:
  • Main text
  • 12967_2018_1605_MOESM3_ESM.xlsx, sheet 1
  • 12967_2018_Article_1605.pdf
View BVdb publication page