SCN5A c.1003T>C ;(p.C335R)

Variant ID: 3-38648297-A-G

NM_000335.4(SCN5A):c.1003T>C;(p.C335R)

This variant was identified in 10 publications

View GRCh38 version.




Publications:


Genetic testing in children with Brugada syndrome: results from a large prospective registry.

Europace : European Pacing, Arrhythmias, And Cardiac Electrophysiology : Journal Of The Working Groups On Cardiac Pacing, Arrhythmias, And Cardiac Cellular Electrophysiology Of The European Society Of Cardiology
Pannone, Luigi L; Bisignani, Antonio A; Osei, Randy R; Gauthey, Anaïs A; Sorgente, Antonio A; Vergara, Pasquale P; Monaco, Cinzia C; Della Rocca, Domenico Giovanni DG; Del Monte, Alvise A; Strazdas, Antanas A; Mojica, Joerelle J; Al Housari, Maysam M; Miraglia, Vincenzo V; Mouram, Sahar S; Paparella, Gaetano G; Ramak, Robbert R; Overeinder, Ingrid I; Bala, Gezim G; Almorad, Alexandre A; Ströker, Erwin E; Pappaert, Gudrun G; Sieira, Juan J; de Ravel, Thomy T; La Meir, Mark M; Brugada, Pedro P; Chierchia, Gian Battista GB; Van Dooren, Sonia S; de Asmundis, Carlo C
Publication Date: 2023-04-16

Variant appearance in text: SCN5A: 1003T>C; Cys335Arg
PubMed Link: 37061847
Variant Present in the following documents:
  • Main text
  • euad079.pdf
View BVdb publication page



Identification of BMP10 as a Novel Gene Contributing to Dilated Cardiomyopathy.

Diagnostics (Basel, Switzerland)
Gu, Jia-Ning JN; Yang, Chen-Xi CX; Ding, Yuan-Yuan YY; Qiao, Qi Q; Di, Ruo-Min RM; Sun, Yu-Min YM; Wang, Jun J; Yang, Ling L; Xu, Ying-Jia YJ; Yang, Yi-Qing YQ
Publication Date: 2023-01-09

Variant appearance in text: SCN5A: C335R
PubMed Link: 36673052
Variant Present in the following documents:
  • diagnostics-13-00242.pdf
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KLF13 Loss-of-Function Mutations Underlying Familial Dilated Cardiomyopathy.

Journal Of The American Heart Association
Guo, Yu-Han YH; Wang, Jun J; Guo, Xiao-Juan XJ; Gao, Ri-Feng RF; Yang, Chen-Xi CX; Li, Li L; Sun, Yu-Min YM; Qiu, Xing-Biao XB; Xu, Ying-Jia YJ; Yang, Yi-Qing YQ
Publication Date: 2022-11-15

Variant appearance in text: SCN5A: C335R
PubMed Link: 36346048
Variant Present in the following documents:
  • JAH3-11-e027578.pdf
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Genotype Complements the Phenotype: Identification of the Pathogenicity of an LMNA Splice Variant by Nanopore Long-Read Sequencing in a Large DCM Family.

International Journal Of Molecular Sciences
Sedaghat-Hamedani, Farbod F; Rebs, Sabine S; Kayvanpour, Elham E; Zhu, Chenchen C; Amr, Ali A; Müller, Marion M; Haas, Jan J; Wu, Jingyan J; Steinmetz, Lars M LM; Ehlermann, Philipp P; Streckfuss-Bömeke, Katrin K; Frey, Norbert N; Meder, Benjamin B
Publication Date: 2022-10-13

Variant appearance in text: SCN5A: C335R
PubMed Link: 36293084
Variant Present in the following documents:
  • ijms-23-12230.pdf
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Gene variant effects across sodium channelopathies predict function and guide precision therapy.

Brain : A Journal Of Neurology
Brunklaus, Andreas A; Feng, Tony T; Brünger, Tobias T; Perez-Palma, Eduardo E; Heyne, Henrike H; Matthews, Emma E; Semsarian, Christopher C; Symonds, Joseph D JD; Zuberi, Sameer M SM; Lal, Dennis D; Schorge, Stephanie S
Publication Date: 2022-01-17

Variant appearance in text: SCN5A: C335R
PubMed Link: 35037686
Variant Present in the following documents:
  • awac006_Supplementary_Data.pdf
View BVdb publication page



Identification of SCN5a p.C335R Variant in a Large Family with Dilated Cardiomyopathy and Conduction Disease.

International Journal Of Molecular Sciences
Sedaghat-Hamedani, Farbod F; Rebs, Sabine S; El-Battrawy, Ibrahim I; Chasan, Safak S; Krause, Tobias T; Haas, Jan J; Zhong, Rujia R; Liao, Zhenxing Z; Xu, Qiang Q; Zhou, Xiaobo X; Akin, Ibrahim I; Zitron, Edgar E; Frey, Norbert N; Streckfuss-Bömeke, Katrin K; Kayvanpour, Elham E
Publication Date: 2021-11-30

Variant appearance in text: SCN5A: 1003T>C
PubMed Link: 34884792
Variant Present in the following documents:
  • Main text
  • ijms-22-12990.pdf
View BVdb publication page



Identification of SCN5a p.C335R Variant in a Large Family with Dilated Cardiomyopathy and Conduction Disease.

International Journal Of Molecular Sciences
Sedaghat-Hamedani, Farbod F; Rebs, Sabine S; El-Battrawy, Ibrahim I; Chasan, Safak S; Krause, Tobias T; Haas, Jan J; Zhong, Rujia R; Liao, Zhenxing Z; Xu, Qiang Q; Zhou, Xiaobo X; Akin, Ibrahim I; Zitron, Edgar E; Frey, Norbert N; Streckfuss-Bömeke, Katrin K; Kayvanpour, Elham E
Publication Date: 2021-11-30

Variant appearance in text: SCN5A: 1003T>C
PubMed Link: 34884792
Variant Present in the following documents:
  • Main text
  • ijms-22-12990.pdf
View BVdb publication page



Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Walsh, Roddy R; Lahrouchi, Najim N; Tadros, Rafik R; Kyndt, Florence F; Glinge, Charlotte C; Postema, Pieter G PG; Amin, Ahmad S AS; Nannenberg, Eline A EA; Ware, James S JS; Whiffin, Nicola N; Mazzarotto, Francesco F; Škorić-Milosavljević, Doris D; Krijger, Christian C; Arbelo, Elena E; Babuty, Dominique D; Barajas-Martinez, Hector H; Beckmann, Britt M BM; Bézieau, Stéphane S; Bos, J Martijn JM; Breckpot, Jeroen J; Campuzano, Oscar O; Castelletti, Silvia S; Celen, Candan C; Clauss, Sebastian S; Corveleyn, Anniek A; Crotti, Lia L; Dagradi, Federica F; de Asmundis, Carlo C; Denjoy, Isabelle I; Dittmann, Sven S; Ellinor, Patrick T PT; Ortuño, Cristina Gil CG; Giustetto, Carla C; Gourraud, Jean-Baptiste JB; Hazeki, Daisuke D; Horie, Minoru M; Ishikawa, Taisuke T; Itoh, Hideki H; Kaneko, Yoshiaki Y; Kanters, Jørgen K JK; Kimoto, Hiroki H; Kotta, Maria-Christina MC; Krapels, Ingrid P C IPC; Kurabayashi, Masahiko M; Lazarte, Julieta J; Leenhardt, Antoine A; Loeys, Bart L BL; Lundin, Catarina C; Makiyama, Takeru T; Mansourati, Jacques J; Martins, Raphaël P RP; Mazzanti, Andrea A; Mörner, Stellan S; Napolitano, Carlo C; Ohkubo, Kimie K; Papadakis, Michael M; Rudic, Boris B; Molina, Maria Sabater MS; Sacher, Frédéric F; Sahin, Hatice H; Sarquella-Brugada, Georgia G; Sebastiano, Regina R; Sharma, Sanjay S; Sheppard, Mary N MN; Shimamoto, Keiko K; Shoemaker, M Benjamin MB; Stallmeyer, Birgit B; Steinfurt, Johannes J; Tanaka, Yuji Y; Tester, David J DJ; Usuda, Keisuke K; van der Zwaag, Paul A PA; Van Dooren, Sonia S; Van Laer, Lut L; Winbo, Annika A; Winkel, Bo G BG; Yamagata, Kenichiro K; Zumhagen, Sven S; Volders, Paul G A PGA; Lubitz, Steven A SA; Antzelevitch, Charles C; Platonov, Pyotr G PG; Odening, Katja E KE; Roden, Dan M DM; Roberts, Jason D JD; Skinner, Jonathan R JR; Tfelt-Hansen, Jacob J; van den Berg, Maarten P MP; Olesen, Morten S MS; Lambiase, Pier D PD; Borggrefe, Martin M; Hayashi, Kenshi K; Rydberg, Annika A; Nakajima, Tadashi T; Yoshinaga, Masao M; Saenen, Johan B JB; Kääb, Stefan S; Brugada, Pedro P; Robyns, Tomas T; Giachino, Daniela F DF; Ackerman, Michael J MJ; Brugada, Ramon R; Brugada, Josep J; Gimeno, Juan R JR; Hasdemir, Can C; Guicheney, Pascale P; Priori, Silvia G SG; Schulze-Bahr, Eric E; Makita, Naomasa N; Schwartz, Peter J PJ; Shimizu, Wataru W; Aiba, Takeshi T; Schott, Jean-Jacques JJ; Redon, Richard R; Ohno, Seiko S; Probst, Vincent V; , ; Behr, Elijah R ER; Barc, Julien J; Bezzina, Connie R CR
Publication Date: 2021-01

Variant appearance in text: SCN5A: 1003T>C; Cys335Arg
PubMed Link: 32893267
Variant Present in the following documents:
  • 41436_2020_946_MOESM2_ESM.xlsx, sheet 3
View BVdb publication page



High-Throughput Reclassification of SCN5A Variants.

American Journal Of Human Genetics
Glazer, Andrew M AM; Wada, Yuko Y; Li, Bian B; Muhammad, Ayesha A; Kalash, Olivia R OR; O'Neill, Matthew J MJ; Shields, Tiffany T; Hall, Lynn L; Short, Laura L; Blair, Marcia A MA; Kroncke, Brett M BM; Capra, John A JA; Roden, Dan M DM
Publication Date: 2020-07-02

Variant appearance in text: SCN5A: Cys335Arg
PubMed Link: 32533946
Variant Present in the following documents:
  • Main text
View BVdb publication page



Dysfunctional Nav1.5 channels due to SCN5A mutations.

Experimental Biology And Medicine (Maywood, N.J.)
Han, Dan D; Tan, Hui H; Sun, Chaofeng C; Li, Guoliang G
Publication Date: 2018-06

Variant appearance in text: SCN5A: C335R
PubMed Link: 29806494
Variant Present in the following documents:
  • Main text
View BVdb publication page