RRAS c.397G>A ;(p.D133N)

Variant ID: 19-50139932-C-T

NM_006270.3(RRAS):c.397G>A;(p.D133N)

This variant was identified in 13 publications

View GRCh38 version.




Publications:


Case Report: A Novel Pathomechanism in PEComa by the Loss of Heterozygosity of TP53.

Frontiers In Oncology
Butz, Henriett H; Lövey, József J; Szentkereszty, Márton M; Bozsik, Anikó A; Tóth, Erika E; Patócs, Attila A
Publication Date: 2022

Variant appearance in text: RRAS: 397G>A; D133N; rs61760904
PubMed Link: 35419288
Variant Present in the following documents:
  • Table_1.xlsx, sheet 1
View BVdb publication page



Rare coding variants in RCN3 are associated with blood pressure.

Bmc Genomics
He, Karen Y KY; Kelly, Tanika N TN; Wang, Heming H; Liang, Jingjing J; Zhu, Luke L; Cade, Brian E BE; Assimes, Themistocles L TL; Becker, Lewis C LC; Beitelshees, Amber L AL; Bielak, Lawrence F LF; Bress, Adam P AP; Brody, Jennifer A JA; Chang, Yen-Pei Christy YC; Chang, Yi-Cheng YC; de Vries, Paul S PS; Duggirala, Ravindranath R; Fox, Ervin R ER; Franceschini, Nora N; Furniss, Anna L AL; Gao, Yan Y; Guo, Xiuqing X; Haessler, Jeffrey J; Hung, Yi-Jen YJ; Hwang, Shih-Jen SJ; Irvin, Marguerite Ryan MR; Kalyani, Rita R RR; Liu, Ching-Ti CT; Liu, Chunyu C; Martin, Lisa Warsinger LW; Montasser, May E ME; Muntner, Paul M PM; Mwasongwe, Stanford S; Naseri, Take T; Palmas, Walter W; Reupena, Muagututi'a Sefuiva MS; Rice, Kenneth M KM; Sheu, Wayne H-H WH; Shimbo, Daichi D; Smith, Jennifer A JA; Snively, Beverly M BM; Yanek, Lisa R LR; Zhao, Wei W; Blangero, John J; Boerwinkle, Eric E; Chen, Yii-Der Ida YI; Correa, Adolfo A; Cupples, L Adrienne LA; Curran, Joanne E JE; Fornage, Myriam M; He, Jiang J; Hou, Lifang L; Kaplan, Robert C RC; Kardia, Sharon L R SLR; Kenny, Eimear E EE; Kooperberg, Charles C; Lloyd-Jones, Donald D; Loos, Ruth J F RJF; Mathias, Rasika A RA; McGarvey, Stephen T ST; Mitchell, Braxton D BD; North, Kari E KE; Peyser, Patricia A PA; Psaty, Bruce M BM; Raffield, Laura M LM; Rao, D C DC; Redline, Susan S; Reiner, Alex P AP; Rich, Stephen S SS; Rotter, Jerome I JI; Taylor, Kent D KD; Tracy, Russell R; Vasan, Ramachandran S RS; , ; Morrison, Alanna C AC; Levy, Daniel D; Chakravarti, Aravinda A; Arnett, Donna K DK; Zhu, Xiaofeng X
Publication Date: 2022-02-19

Variant appearance in text: rs61760904
PubMed Link: 35183128
Variant Present in the following documents:
  • Main text
  • 12864_2022_Article_8356.pdf
View BVdb publication page



Comparative and Functional Genomic Resource for Mechanistic Studies of Human Blood Pressure-Associated Single Nucleotide Polymorphisms.

Hypertension (Dallas, Tex. : 1979)
Mishra, Manoj K MK; Liang, Eugene Y EY; Geurts, Aron M AM; Auer, Paul W L PWL; Liu, Pengyuan P; Rao, Sridhar S; Greene, Andrew S AS; Liang, Mingyu M; Liu, Yong Y
Publication Date: 2020-03

Variant appearance in text: rs61760904
PubMed Link: 31902252
Variant Present in the following documents:
  • Main text
View BVdb publication page



Evolving neoantigen profiles in colorectal cancers with DNA repair defects.

Genome Medicine
Rospo, Giuseppe G; Lorenzato, Annalisa A; Amirouchene-Angelozzi, Nabil N; Magrì, Alessandro A; Cancelliere, Carlotta C; Corti, Giorgio G; Negrino, Carola C; Amodio, Vito V; Montone, Monica M; Bartolini, Alice A; Barault, Ludovic L; Novara, Luca L; Isella, Claudio C; Medico, Enzo E; Bertotti, Andrea A; Trusolino, Livio L; Germano, Giovanni G; Di Nicolantonio, Federica F; Bardelli, Alberto A
Publication Date: 2019-06-28

Variant appearance in text: RRAS: D133N
PubMed Link: 31253177
Variant Present in the following documents:
  • 13073_2019_654_MOESM2_ESM.xlsx, sheet 59
  • 13073_2019_654_MOESM2_ESM.xlsx, sheet 31
View BVdb publication page



Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.

Nature Genetics
Giri, Ayush A; Hellwege, Jacklyn N JN; Keaton, Jacob M JM; Park, Jihwan J; Qiu, Chengxiang C; Warren, Helen R HR; Torstenson, Eric S ES; Kovesdy, Csaba P CP; Sun, Yan V YV; Wilson, Otis D OD; Robinson-Cohen, Cassianne C; Roumie, Christianne L CL; Chung, Cecilia P CP; Birdwell, Kelly A KA; Damrauer, Scott M SM; DuVall, Scott L SL; Klarin, Derek D; Cho, Kelly K; Wang, Yu Y; Evangelou, Evangelos E; Cabrera, Claudia P CP; Wain, Louise V LV; Shrestha, Rojesh R; Mautz, Brian S BS; Akwo, Elvis A EA; Sargurupremraj, Muralidharan M; Debette, Stéphanie S; Boehnke, Michael M; Scott, Laura J LJ; Luan, Jian'an J; Zhao, Jing-Hua JH; Willems, Sara M SM; Thériault, Sébastien S; Shah, Nabi N; Oldmeadow, Christopher C; Almgren, Peter P; Li-Gao, Ruifang R; Verweij, Niek N; Boutin, Thibaud S TS; Mangino, Massimo M; Ntalla, Ioanna I; Feofanova, Elena E; Surendran, Praveen P; Cook, James P JP; Karthikeyan, Savita S; Lahrouchi, Najim N; Liu, Chunyu C; Sepúlveda, Nuno N; Richardson, Tom G TG; Kraja, Aldi A; Amouyel, Philippe P; Farrall, Martin M; Poulter, Neil R NR; , ; , ; , ; Laakso, Markku M; Zeggini, Eleftheria E; Sever, Peter P; Scott, Robert A RA; Langenberg, Claudia C; Wareham, Nicholas J NJ; Conen, David D; Palmer, Colin Neil Alexander CNA; Attia, John J; Chasman, Daniel I DI; Ridker, Paul M PM; Melander, Olle O; Mook-Kanamori, Dennis Owen DO; Harst, Pim van der PV; Cucca, Francesco F; Schlessinger, David D; Hayward, Caroline C; Spector, Tim D TD; Jarvelin, Marjo-Riitta MR; Hennig, Branwen J BJ; Timpson, Nicholas J NJ; Wei, Wei-Qi WQ; Smith, Joshua C JC; Xu, Yaomin Y; Matheny, Michael E ME; Siew, Edward E EE; Lindgren, Cecilia C; Herzig, Karl-Heinz KH; Dedoussis, George G; Denny, Joshua C JC; Psaty, Bruce M BM; Howson, Joanna M M JMM; Munroe, Patricia B PB; Newton-Cheh, Christopher C; Caulfield, Mark J MJ; Elliott, Paul P; Gaziano, J Michael JM; Concato, John J; Wilson, Peter W F PWF; Tsao, Philip S PS; Velez Edwards, Digna R DR; Susztak, Katalin K; , ; O'Donnell, Christopher J CJ; Hung, Adriana M AM; Edwards, Todd L TL
Publication Date: 2019-01

Variant appearance in text: rs61760904
PubMed Link: 30578418
Variant Present in the following documents:
  • Main text
  • nihms-1511350.pdf
  • NIHMS1511350-supplement-1.pdf
View BVdb publication page



Whole-exon sequencing of human myeloma cell lines shows mutations related to myeloma patients at relapse with major hits in the DNA regulation and repair pathways.

Journal Of Hematology & Oncology
Tessoulin, Benoît B; Moreau-Aubry, Agnès A; Descamps, Géraldine G; Gomez-Bougie, Patricia P; Maïga, Sophie S; Gaignard, Alban A; Chiron, David D; Ménoret, Emmanuelle E; Le Gouill, Steven S; Moreau, Philippe P; Amiot, Martine M; Pellat-Deceunynck, Catherine C
Publication Date: 2018-12-13

Variant appearance in text: RRAS: 397G>A; D133N; rs61760904
PubMed Link: 30545397
Variant Present in the following documents:
  • 13045_2018_679_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Brief Overview of a Decade of Genome-Wide Association Studies on Primary Hypertension.

International Journal Of Endocrinology
Azam, Afifah Binti AB; Azizan, Elena Aisha Binti EAB
Publication Date: 2018

Variant appearance in text: rs61760904
PubMed Link: 29666641
Variant Present in the following documents:
  • Main text
  • IJE2018-7259704.pdf
View BVdb publication page



Detecting protein variants by mass spectrometry: a comprehensive study in cancer cell-lines.

Genome Medicine
Alfaro, Javier A JA; Ignatchenko, Alexandr A; Ignatchenko, Vladimir V; Sinha, Ankit A; Boutros, Paul C PC; Kislinger, Thomas T
Publication Date: 2017-07-18

Variant appearance in text: RRAS: D133N; rs61760904
PubMed Link: 28716134
Variant Present in the following documents:
  • 13073_2017_454_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page



Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.

Nature Genetics
Surendran, Praveen P; Drenos, Fotios F; Young, Robin R; Warren, Helen H; Cook, James P JP; Manning, Alisa K AK; Grarup, Niels N; Sim, Xueling X; Barnes, Daniel R DR; Witkowska, Kate K; Staley, James R JR; Tragante, Vinicius V; Tukiainen, Taru T; Yaghootkar, Hanieh H; Masca, Nicholas N; Freitag, Daniel F DF; Ferreira, Teresa T; Giannakopoulou, Olga O; Tinker, Andrew A; Harakalova, Magdalena M; Mihailov, Evelin E; Liu, Chunyu C; Kraja, Aldi T AT; Fallgaard Nielsen, Sune S; Rasheed, Asif A; Samuel, Maria M; Zhao, Wei W; Bonnycastle, Lori L LL; Jackson, Anne U AU; Narisu, Narisu N; Swift, Amy J AJ; Southam, Lorraine L; Marten, Jonathan J; Huyghe, Jeroen R JR; Stančáková, Alena A; Fava, Cristiano C; Ohlsson, Therese T; Matchan, Angela A; Stirrups, Kathleen E KE; Bork-Jensen, Jette J; Gjesing, Anette P AP; Kontto, Jukka J; Perola, Markus M; Shaw-Hawkins, Susan S; Havulinna, Aki S AS; Zhang, He H; Donnelly, Louise A LA; Groves, Christopher J CJ; Rayner, N William NW; Neville, Matt J MJ; Robertson, Neil R NR; Yiorkas, Andrianos M AM; Herzig, Karl-Heinz KH; Kajantie, Eero E; Zhang, Weihua W; Willems, Sara M SM; Lannfelt, Lars L; Malerba, Giovanni G; Soranzo, Nicole N; Trabetti, Elisabetta E; Verweij, Niek N; Evangelou, Evangelos E; Moayyeri, Alireza A; Vergnaud, Anne-Claire AC; Nelson, Christopher P CP; Poveda, Alaitz A; Varga, Tibor V TV; Caslake, Muriel M; de Craen, Anton Jm AJ; Trompet, Stella S; Luan, Jian'an J; Scott, Robert A RA; Harris, Sarah E SE; Liewald, David Cm DC; Marioni, Riccardo R; Menni, Cristina C; Farmaki, Aliki-Eleni AE; Hallmans, Göran G; Renström, Frida F; Huffman, Jennifer E JE; Hassinen, Maija M; Burgess, Stephen S; Vasan, Ramachandran S RS; Felix, Janine F JF; , ; Uria-Nickelsen, Maria M; Malarstig, Anders A; Reily, Dermot F DF; Hoek, Maarten M; Vogt, Thomas T; Lin, Honghuang H; Lieb, Wolfgang W; , ; Traylor, Matthew M; Markus, Hugh F HF; , ; Highland, Heather M HM; Justice, Anne E AE; Marouli, Eirini E; , ; Lindström, Jaana J; Uusitupa, Matti M; Komulainen, Pirjo P; Lakka, Timo A TA; Rauramaa, Rainer R; Polasek, Ozren O; Rudan, Igor I; Rolandsson, Olov O; Franks, Paul W PW; Dedoussis, George G; Spector, Timothy D TD; , ; Jousilahti, Pekka P; Männistö, Satu S; Deary, Ian J IJ; Starr, John M JM; Langenberg, Claudia C; Wareham, Nick J NJ; Brown, Morris J MJ; Dominiczak, Anna F AF; Connell, John M JM; Jukema, J Wouter JW; Sattar, Naveed N; Ford, Ian I; Packard, Chris J CJ; Esko, Tõnu T; Mägi, Reedik R; Metspalu, Andres A; de Boer, Rudolf A RA; van der Meer, Peter P; van der Harst, Pim P; , ; Gambaro, Giovanni G; Ingelsson, Erik E; Lind, Lars L; de Bakker, Paul Iw PI; Numans, Mattijs E ME; Brandslund, Ivan I; Christensen, Cramer C; Petersen, Eva Rb ER; Korpi-Hyövälti, Eeva E; Oksa, Heikki H; Chambers, John C JC; Kooner, Jaspal S JS; Blakemore, Alexandra If AI; Franks, Steve S; Jarvelin, Marjo-Riitta MR; Husemoen, Lise L LL; Linneberg, Allan A; Skaaby, Tea T; Thuesen, Betina B; Karpe, Fredrik F; Tuomilehto, Jaakko J; Doney, Alex Sf AS; Morris, Andrew D AD; Palmer, Colin Na CN; Holmen, Oddgeir Lingaas OL; Hveem, Kristian K; Willer, Cristen J CJ; Tuomi, Tiinamaija T; Groop, Leif L; Käräjämäki, AnneMari A; Palotie, Aarno A; Ripatti, Samuli S; Salomaa, Veikko V; Alam, Dewan S DS; Shafi Majumder, Abdulla Al AA; Di Angelantonio, Emanuele E; Chowdhury, Rajiv R; McCarthy, Mark I MI; Poulter, Neil N; Stanton, Alice V AV; Sever, Peter P; Amouyel, Philippe P; Arveiler, Dominique D; Blankenberg, Stefan S; Ferrières, Jean J; Kee, Frank F; Kuulasmaa, Kari K; Müller-Nurasyid, Martina M; Veronesi, Giovanni G; Virtamo, Jarmo J; Deloukas, Panos P; , ; Elliott, Paul P; , ; Zeggini, Eleftheria E; Kathiresan, Sekar S; Melander, Olle O; Kuusisto, Johanna J; Laakso, Markku M; Padmanabhan, Sandosh S; Porteous, David D; Hayward, Caroline C; Scotland, Generation G; Collins, Francis S FS; Mohlke, Karen L KL; Hansen, Torben T; Pedersen, Oluf O; Boehnke, Michael M; Stringham, Heather M HM; , ; Frossard, Philippe P; Newton-Cheh, Christopher C; , ; Tobin, Martin D MD; Nordestgaard, Børge Grønne BG; , ; , ; , ; , ; Caulfield, Mark J MJ; Mahajan, Anubha A; Morris, Andrew P AP; Tomaszewski, Maciej M; Samani, Nilesh J NJ; Saleheen, Danish D; Asselbergs, Folkert W FW; Lindgren, Cecilia M CM; Danesh, John J; Wain, Louise V LV; Butterworth, Adam S AS; Howson, Joanna Mm JM; Munroe, Patricia B PB
Publication Date: 2016-10

Variant appearance in text: rs61760904
PubMed Link: 27618447
Variant Present in the following documents:
  • Main text
  • NIHMS69533-supplement-Supplementary_Tables.xlsx, sheet 16
  • NIHMS69533-supplement-Supplementary_Tables.xlsx, sheet 5
  • emss-69533.pdf
View BVdb publication page



Patients with genetically heterogeneous synchronous colorectal cancer carry rare damaging germline mutations in immune-related genes.

Nature Communications
Cereda, Matteo M; Gambardella, Gennaro G; Benedetti, Lorena L; Iannelli, Fabio F; Patel, Dominic D; Basso, Gianluca G; Guerra, Rosalinda F RF; Mourikis, Thanos P TP; Puccio, Ignazio I; Sinha, Shruti S; Laghi, Luigi L; Spencer, Jo J; Rodriguez-Justo, Manuel M; Ciccarelli, Francesca D FD
Publication Date: 2016-07-05

Variant appearance in text: RRAS: D133N
PubMed Link: 27377421
Variant Present in the following documents:
  • ncomms12072-s6.xlsx, sheet 1
View BVdb publication page



XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.

Plos One
Talukder, Asoke K AK; Ravishankar, Shashidhar S; Sasmal, Krittika K; Gandham, Santhosh S; Prabhukumar, Jyothsna J; Achutharao, Prahalad H PH; Barh, Debmalya D; Blasi, Francesco F
Publication Date: 2015

Variant appearance in text: RRAS: D133N; rs61760904
PubMed Link: 25905921
Variant Present in the following documents:
  • pone.0123569.s008.xls, sheet 1
View BVdb publication page



Integrated analysis of germline and somatic variants in ovarian cancer.

Nature Communications
Kanchi, Krishna L KL; Johnson, Kimberly J KJ; Lu, Charles C; McLellan, Michael D MD; Leiserson, Mark D M MD; Wendl, Michael C MC; Zhang, Qunyuan Q; Koboldt, Daniel C DC; Xie, Mingchao M; Kandoth, Cyriac C; McMichael, Joshua F JF; Wyczalkowski, Matthew A MA; Larson, David E DE; Schmidt, Heather K HK; Miller, Christopher A CA; Fulton, Robert S RS; Spellman, Paul T PT; Mardis, Elaine R ER; Druley, Todd E TE; Graubert, Timothy A TA; Goodfellow, Paul J PJ; Raphael, Benjamin J BJ; Wilson, Richard K RK; Ding, Li L
Publication Date: 2014

Variant appearance in text: RRAS: D133N
PubMed Link: 24448499
Variant Present in the following documents:
  • NIHMS551112-supplement-9.xlsx, sheet 1
  • NIHMS551112-supplement-7.xlsx, sheet 1
View BVdb publication page