MYH7 c.4644+190C>T

Variant ID: 14-23885887-G-A

NM_000257.2(MYH7):c.4644+190C>T

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs3729829
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Exploration of Potential Genetic Biomarkers for Heart Failure: A Systematic Review.

International Journal Of Environmental Research And Public Health
Chair, Sek Ying SY; Chan, Judy Yuet Wa JYW; Waye, Mary Miu Yee MMY; Liu, Ting T; Law, Bernard Man Hin BMH; Chien, Wai Tong WT
Publication Date: 2021-05-31

Variant appearance in text: rs3729829
PubMed Link: 34072866
Variant Present in the following documents:
  • Main text
  • ijerph-18-05904.pdf
View BVdb publication page



Biomarkers for Heart Failure Prognosis: Proteins, Genetic Scores and Non-coding RNAs.

Frontiers In Cardiovascular Medicine
Shrivastava, Apurva A; Haase, Tina T; Zeller, Tanja T; Schulte, Christian C
Publication Date: 2020

Variant appearance in text: rs3729829
PubMed Link: 33330662
Variant Present in the following documents:
  • Main text
  • fcvm-07-601364.pdf
View BVdb publication page



Association of long-chain non-coding RNA MHRT gene single nucleotide polymorphism with risk and prognosis of chronic heart failure.

Medicine
Zhang, Gao G; Dou, Liping L; Chen, Yuanyuan Y
Publication Date: 2020-07-17

Variant appearance in text: rs3729829
PubMed Link: 32702806
Variant Present in the following documents:
  • Main text
  • medi-99-e19703.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: MYH7: 4644+190C>T; rs3729829
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
View BVdb publication page



Fetal cardiac troponin isoforms rescue the increased Ca2+ sensitivity produced by a novel double deletion in cardiac troponin T linked to restrictive cardiomyopathy: a clinical, genetic, and functional approach.

The Journal Of Biological Chemistry
Pinto, Jose Renato JR; Yang, Shi Wei SW; Hitz, Marc-Phillip MP; Parvatiyar, Michelle S MS; Jones, Michelle A MA; Liang, Jingsheng J; Kokta, Victor V; Talajic, Mario M; Tremblay, Nicolas N; Jaeggi, Michelle M; Andelfinger, Gregor G; Potter, James D JD
Publication Date: 2011-06-10

Variant appearance in text: rs3729829
PubMed Link: 21502316
Variant Present in the following documents:
  • Main text
View BVdb publication page