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