MYH7 c.4835T>C ;(p.L1612P)

Variant ID: 14-23885331-A-G

NM_000257.2(MYH7):c.4835T>C;(p.L1612P)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Disease mutations in striated muscle myosins.

Biophysical Reviews
Parker, Francine F; Peckham, Michelle M
Publication Date: 2020-08

Variant appearance in text: MYH7: Leu1612Pro
PubMed Link: 32651905
Variant Present in the following documents:
  • 12551_2020_721_MOESM1_ESM.pdf
View BVdb publication page



Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes.

Circulation. Genomic And Precision Medicine
Ingles, Jodie J; Goldstein, Jennifer J; Thaxton, Courtney C; Caleshu, Colleen C; Corty, Edward W EW; Crowley, Stephanie B SB; Dougherty, Kristen K; Harrison, Steven M SM; McGlaughon, Jennifer J; Milko, Laura V LV; Morales, Ana A; Seifert, Bryce A BA; Strande, Natasha N; Thomson, Kate K; Peter van Tintelen, J J; Wallace, Kathleen K; Walsh, Roddy R; Wells, Quinn Q; Whiffin, Nicola N; Witkowski, Leora L; Semsarian, Christopher C; Ware, James S JS; Hershberger, Ray E RE; Funke, Birgit B
Publication Date: 2019-02

Variant appearance in text: MYH7: 4835T>C; Leu1612Pro
PubMed Link: 30681346
Variant Present in the following documents:
  • hcg-12-e002460-s002.xlsx, sheet 8
View BVdb publication page



Sources of discordance among germ-line variant classifications in ClinVar.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Yang, Shan S; Lincoln, Stephen E SE; Kobayashi, Yuya Y; Nykamp, Keith K; Nussbaum, Robert L RL; Topper, Scott S
Publication Date: 2017-10

Variant appearance in text: MYH7: 4835T>C; Leu1612Pro
PubMed Link: 28569743
Variant Present in the following documents:
  • gim201760x7.xlsx, sheet 2
View BVdb publication page



The sarcomeric M-region: a molecular command center for diverse cellular processes.

Biomed Research International
Hu, Li-Yen R LY; Ackermann, Maegen A MA; Kontrogianni-Konstantopoulos, Aikaterini A
Publication Date: 2015

Variant appearance in text: MPD1: L1612P
PubMed Link: 25961035
Variant Present in the following documents:
  • Main text
  • BMRI2015-714197.pdf
View BVdb publication page



Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy.

Human Mutation
Lamont, Phillipa J PJ; Wallefeld, William W; Hilton-Jones, David D; Udd, Bjarne B; Argov, Zohar Z; Barboi, Alexandru C AC; Bonneman, Carsten C; Boycott, Kym M KM; Bushby, Kate K; Connolly, Anne M AM; Davies, Nicholas N; Beggs, Alan H AH; Cox, Gerald F GF; Dastgir, Jahannaz J; DeChene, Elizabeth T ET; Gooding, Rebecca R; Jungbluth, Heinz H; Muelas, Nuria N; Palmio, Johanna J; Penttilä, Sini S; Schmedding, Eric E; Suominen, Tiina T; Straub, Volker V; Staples, Christopher C; Van den Bergh, Peter Y K PY; Vilchez, Juan J JJ; Wagner, Kathryn R KR; Wheeler, Patricia G PG; Wraige, Elizabeth E; Laing, Nigel G NG
Publication Date: 2014-07

Variant appearance in text: MYH7: 4835T>C
PubMed Link: 24664454
Variant Present in the following documents:
  • Main text
View BVdb publication page