MYH7 c.3388G>A ;(p.A1130T)

Variant ID: 14-23889392-C-T

NM_000257.2(MYH7):c.3388G>A;(p.A1130T)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Identification of Immune-Related Gene Signatures in Lung Adenocarcinoma and Lung Squamous Cell Carcinoma.

Frontiers In Immunology
Li, Na N; Wang, Jiahong J; Zhan, Xianquan X
Publication Date: 2021

Variant appearance in text: MYH7: 3388G>A; Ala1130Thr
PubMed Link: 34887858
Variant Present in the following documents:
  • Table_4.xlsx, sheet 1
View BVdb publication page



Targeted Next-Generation Sequencing Reveals Hot Spots and Doubly Heterozygous Mutations in Chinese Patients with Familial Cardiomyopathy.

Biomed Research International
Zhao, Yue Y; Feng, Yue Y; Zhang, Yun-Mei YM; Ding, Xiao-Xue XX; Song, Yu-Zhu YZ; Zhang, A-Mei AM; Liu, Li L; Zhang, Hong H; Ding, Jia-Huan JH; Xia, Xue-Shan XS
Publication Date: 2015

Variant appearance in text: MYH7: 3388G>A; Ala1130Thr
PubMed Link: 26199943
Variant Present in the following documents:
  • BMRI2015-561819.pdf
View BVdb publication page



Comparison of the Illumina Genome Analyzer and Roche 454 GS FLX for resequencing of hypertrophic cardiomyopathy-associated genes.

Journal Of Biomolecular Techniques : Jbt
Dames, Shale S; Durtschi, Jacob J; Geiersbach, Katherine K; Stephens, Jack J; Voelkerding, Karl V KV
Publication Date: 2010-07

Variant appearance in text: MYH7: A1130T
PubMed Link: 20592870
Variant Present in the following documents:
  • Main text
View BVdb publication page