COMT c.214G>T ;(p.A72S)

Variant ID: 22-19950263-G-T

NM_000754.3(COMT):c.214G>T;(p.A72S)

This variant was identified in 74 publications

View GRCh38 version.




Publications:


Pharmacogenomic profile of actionable molecular variants related to drugs commonly used in anesthesia: WES analysis reveals new mutations.

Frontiers In Pharmacology
Parada-Márquez, Juan Fernando JF; Maldonado-Rodriguez, Nicolás David ND; Triana-Fonseca, Paula P; Contreras-Bravo, Nora Constanza NC; Calderón-Ospina, Carlos Alberto CA; Restrepo, Carlos M CM; Morel, Adrien A; Ortega-Recalde, Oscar Javier OJ; Silgado-Guzmán, Daniel Felipe DF; Angulo-Aguado, Mariana M; Fonseca-Mendoza, Dora Janeth DJ
Publication Date: 2023

Variant appearance in text: rs6267
PubMed Link: 37021041
Variant Present in the following documents:
  • Table3.xlsx, sheet 1
View BVdb publication page



Integrative single-cell analysis reveals transcriptional and epigenetic regulatory features of clear cell renal cell carcinoma.

Cancer Research
Yu, Zhenyuan Z; Lv, Yufang Y; Su, Cheng C; Lu, Wenhao W; Zhang, RuiRui R; Li, Jiaping J; Guo, Bingqian B; Yan, Haibiao H; Liu, Deyun D; Yang, Zhanbin Z; Mi, Hua H; Mo, Linjian L; Guo, Yi Y; Feng, Wenyu W; Xu, Haotian H; Peng, Wenyi W; Cheng, Jiwen J; Nan, Aruo A; Mo, Zengnan Z
Publication Date: 2023-01-06

Variant appearance in text: COMT: A72S; rs6267
PubMed Link: 36607615
Variant Present in the following documents:
  • can-22-2224_table_s8_suppst8.xlsx, sheet 12
  • can-22-2224_table_s8_suppst8.xlsx, sheet 7
View BVdb publication page



Impact of cognition-related single nucleotide polymorphisms on brain imaging phenotype in Parkinson's disease.

Neural Regeneration Research
Shen, Ting T; Pu, Jia-Li JL; Jiang, Ya-Si YS; Yue, Yu-Mei YM; He, Ting-Ting TT; Qu, Bo-Yi BY; Zhao, Shuai S; Yan, Ya-Ping YP; Lai, Hsin-Yi HY; Zhang, Bao-Rong BR
Publication Date: 2023-05

Variant appearance in text: rs6267
PubMed Link: 36255006
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sex hormone-related polymorphisms in endometriosis and migraine: A narrative review.

Women'S Health (London, England)
van der Vaart, Joy-Fleur JF; Merki-Feld, Gabriele Susanne GS
Publication Date: 2022

Variant appearance in text: rs6267
PubMed Link: 35848345
Variant Present in the following documents:
  • Main text
  • 10.1177_17455057221111315.pdf
View BVdb publication page



Brain Radiotoxicity-Related 15CAcBRT Gene Expression Signature Predicts Survival Prognosis of Glioblastoma Patients.

Neuro-Oncology
Reyes-González, Jesús J; Barajas-Olmos, Francisco F; García-Ortiz, Humberto H; Magraner-Pardo, Lorena L; Pons, Tirso T; Moreno, Sergio S; Aguirre-Cruz, Lucinda L; Reyes-Abrahantes, Andy A; Martínez-Hernández, Angélica A; Contreras-Cubas, Cecilia C; Barrios-Payan, Jorge J; Ruiz-Garcia, Henry J HJ; Hernandez-Pando, Rogelio R; Quiñones-Hinojosa, Alfredo A; Orozco, Lorena L; Abrahantes-Pérez, María Del Carmen MDC
Publication Date: 2022-07-08

Variant appearance in text: COMT: A72S
PubMed Link: 35802478
Variant Present in the following documents:
  • Main text
  • noac171.pdf
  • noac171_suppl_suplementary_table_s7.xlsx, sheet 1
  • noac171_suppl_suplementary_table_s1.xlsx, sheet 1
  • noac171_suppl_suplementary_table_ss9.xls, sheet 1
View BVdb publication page



Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.

Nature Communications
Yin, Xianyong X; Chan, Lap Sum LS; Bose, Debraj D; Jackson, Anne U AU; VandeHaar, Peter P; Locke, Adam E AE; Fuchsberger, Christian C; Stringham, Heather M HM; Welch, Ryan R; Yu, Ketian K; Fernandes Silva, Lilian L; Service, Susan K SK; Zhang, Daiwei D; Hector, Emily C EC; Young, Erica E; Ganel, Liron L; Das, Indraniel I; Abel, Haley H; Erdos, Michael R MR; Bonnycastle, Lori L LL; Kuusisto, Johanna J; Stitziel, Nathan O NO; Hall, Ira M IM; Wagner, Gregory R GR; , ; Kang, Jian J; Morrison, Jean J; Burant, Charles F CF; Collins, Francis S FS; Ripatti, Samuli S; Palotie, Aarno A; Freimer, Nelson B NB; Mohlke, Karen L KL; Scott, Laura J LJ; Wen, Xiaoquan X; Fauman, Eric B EB; Laakso, Markku M; Boehnke, Michael M
Publication Date: 2022-03-28

Variant appearance in text: rs6267
PubMed Link: 35347128
Variant Present in the following documents:
  • Main text
  • 41467_2022_Article_29143.pdf
View BVdb publication page



Genetic overlap between temporomandibular disorders and primary headaches: A systematic review.

The Japanese Dental Science Review
Cruz, Diogo D; Monteiro, Francisca F; Paço, Maria M; Vaz-Silva, Manuel M; Lemos, Carolina C; Alves-Ferreira, Miguel M; Pinho, Teresa T
Publication Date: 2022-11

Variant appearance in text: rs6267
PubMed Link: 35242249
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



COMT Val/Met and Psychopathic Traits in Children and Adolescents: A Systematic Review and New Evidence of a Developmental Trajectory toward Psychopathy.

International Journal Of Molecular Sciences
Kant, Tuana T; Koyama, Emiko E; Zai, Clement C CC; Beitchman, Joseph H JH; Kennedy, James L JL
Publication Date: 2022-02-04

Variant appearance in text: COMT: Ala72Ser; rs6267
PubMed Link: 35163702
Variant Present in the following documents:
  • Main text
  • ijms-23-01782.pdf
View BVdb publication page



COMT Val/Met and Psychopathic Traits in Children and Adolescents: A Systematic Review and New Evidence of a Developmental Trajectory toward Psychopathy.

International Journal Of Molecular Sciences
Kant, Tuana T; Koyama, Emiko E; Zai, Clement C CC; Beitchman, Joseph H JH; Kennedy, James L JL
Publication Date: 2022-02-04

Variant appearance in text: COMT: Ala72Ser; rs6267
PubMed Link: 35163702
Variant Present in the following documents:
  • Main text
  • ijms-23-01782.pdf
View BVdb publication page



Genetic and Clinical Factors Associated with Opioid Response in Chinese Han Patients with Cancer Pain: An Exploratory Cross-Sectional Study.

Pain And Therapy
Shi, Chen C; Liu, Jinmei J; Hu, Jianli J; Chen, Xu X; Xie, Jiyi J; Luo, Juan J; Wang, Cong C; Wang, Hanxiang H; Yuan, Qi Q; Zhu, Haixia H; Gong, Weijing W; Li, Shijun S; Zhou, Hong H; Wang, Leiyun L; Wang, Hui H; Zhang, Yu Y
Publication Date: 2022-03

Variant appearance in text: rs6267
PubMed Link: 35107781
Variant Present in the following documents:
  • Main text
  • 40122_2022_Article_353.pdf
View BVdb publication page



AKR1A1 Variant Associated With Schizophrenia Causes Exon Skipping, Leading to Loss of Enzymatic Activity.

Frontiers In Genetics
Iino, Kyoka K; Toriumi, Kazuya K; Agarie, Riko R; Miyashita, Mitsuhiro M; Suzuki, Kazuhiro K; Horiuchi, Yasue Y; Niizato, Kazuhiro K; Oshima, Kenichi K; Imai, Atsushi A; Nagase, Yukihiro Y; Kushima, Itaru I; Koike, Shinsuke S; Ikegame, Tempei T; Jinde, Seiichiro S; Nagata, Eiichiro E; Washizuka, Shinsuke S; Miyata, Toshio T; Takizawa, Shunya S; Hashimoto, Ryota R; Kasai, Kiyoto K; Ozaki, Norio N; Itokawa, Masanari M; Arai, Makoto M
Publication Date: 2021

Variant appearance in text: COMT: Ala72Ser
PubMed Link: 34938315
Variant Present in the following documents:
  • fgene-12-762999.pdf
View BVdb publication page



Interaction between dietary total antioxidant capacity and BDNF Val66Met polymorphism on lipid profiles and atherogenic indices among diabetic patients.

Scientific Reports
Abaj, Faezeh F; Rafiee, Masoumeh M; Koohdani, Fariba F
Publication Date: 2021-09-27

Variant appearance in text: rs6267
PubMed Link: 34580389
Variant Present in the following documents:
  • Main text
  • 41598_2021_Article_98663.pdf
View BVdb publication page



An overview of pain in Parkinson's disease.

Clinical Parkinsonism & Related Disorders
Tai, Yi-Cheng YC; Lin, Chin-Hsien CH
Publication Date: 2020

Variant appearance in text: rs6267
PubMed Link: 34316612
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Association of FAAH p.Pro129Thr and COMT p.Ala72Ser with schizophrenia and comorbid substance use through next-generation sequencing: an exploratory analysis.

Revista Brasileira De Psiquiatria (Sao Paulo, Brazil : 1999)
Martínez-Magaña, José J JJ; Genis-Mendoza, Alma D AD; González-Covarrubias, Vanessa V; Juárez-Rojop, Isela E IE; Tovilla-Zárate, Carlos A CA; Soberón, Xavier X; Lanzagorta, Nuria N; Nicolini, Humberto H
Publication Date: 2022

Variant appearance in text: COMT: Ala72Ser; rs6267
PubMed Link: 34037083
Variant Present in the following documents:
  • Main text
  • bjp-44-02-164.pdf
View BVdb publication page



Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology
Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA
Publication Date: 2021

Variant appearance in text: COMT: A72S; rs6267
PubMed Link: 33791233
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Actionable pharmacogenetic variants in Hong Kong Chinese exome sequencing data and projected prescription impact in the Hong Kong population.

Plos Genetics
Yu, Mullin Ho Chung MHC; Chan, Marcus Chun Yin MCY; Chung, Claudia Ching Yan CCY; Li, Andrew Wang Tat AWT; Yip, Chara Yin Wa CYW; Mak, Christopher Chun Yu CCY; Chau, Jeffrey Fong Ting JFT; Lee, Mianne M; Fung, Jasmine Lee Fong JLF; Tsang, Mandy Ho Yin MHY; Chan, Joshua Chun Ki JCK; Wong, Wilfred Hing Sang WHS; Yang, Jing J; Chui, William Chun Ming WCM; Chung, Patrick Ho Yu PHY; Yang, Wanling W; Lee, So Lun SL; Chan, Godfrey Chi Fung GCF; Tam, Paul Kwong Hang PKH; Lau, Yu Lung YL; Tang, Clara Sze Man CSM; Yeung, Kit San KS; Chung, Brian Hon Yin BHY
Publication Date: 2021-02

Variant appearance in text: rs6267
PubMed Link: 33600428
Variant Present in the following documents:
  • pgen.1009323.s010.xlsx, sheet 1
View BVdb publication page



Association Between the COMT Val158Met Polymorphism and Antipsychotic Efficacy in Schizophrenia: An Updated Meta-Analysis.

Current Neuropharmacology
Ma, Jingsong J; Zhao, Mingzhe M; Zhou, Wei W; Li, Mo M; Huai, Cong C; Shen, Lu L; Wang, Ting T; Wu, Hao H; Zhang, Na N; Zhang, Zhiruo Z; He, Lin L; Qin, Shengying S
Publication Date: 2021

Variant appearance in text: rs6267
PubMed Link: 33100205
Variant Present in the following documents:
  • Main text
  • CN-19-1780.pdf
View BVdb publication page



The Association Analysis of GPNMB rs156429 With Clinical Manifestations in Chinese Population With Parkinson's Disease.

Frontiers In Genetics
Liu, Jin J; Li, Gen G; He, Yixi Y; He, Guiying G; Zhang, Pingchen P; Shen, Xin X; Zhang, Weishan W; Chen, Shengdi S; Cui, Shishuang S; Tan, Yuyan Y
Publication Date: 2020

Variant appearance in text: rs6267
PubMed Link: 32983228
Variant Present in the following documents:
  • Main text
  • fgene-11-00952.pdf
View BVdb publication page



The advances of genetics research on Hirschsprung's disease.

Pediatric Investigation
Ke, Juntao J; Zhu, Ying Y; Miao, Xiaoping X
Publication Date: 2018-09

Variant appearance in text: COMT: Ala72Ser; rs6267
PubMed Link: 32851260
Variant Present in the following documents:
  • Main text
  • PED4-2-189.pdf
View BVdb publication page



Genetic Markers for Later Remission in Response to Early Improvement of Antidepressants.

International Journal Of Molecular Sciences
Kang, Hee-Ju HJ; Kim, Ki-Tae KT; Yoo, Kyung-Hun KH; Park, Yoomi Y; Kim, Ju-Wan JW; Kim, Sung-Wan SW; Shin, Il-Seon IS; Kim, Ju Han JH; Kim, Jae-Min JM
Publication Date: 2020-07-10

Variant appearance in text: COMT: Ala72Ser; rs6267
PubMed Link: 32664413
Variant Present in the following documents:
  • Main text
  • ijms-21-04884.pdf
  • ijms-21-04884-s001.pdf
View BVdb publication page



Pharmacogenetics of Antipsychotic Drug Treatment: Update and Clinical Implications.

Molecular Neuropsychiatry
Yoshida, Kazunari K; Müller, Daniel J DJ
Publication Date: 2020-04

Variant appearance in text: rs6267
PubMed Link: 32399466
Variant Present in the following documents:
  • Main text
View BVdb publication page



Cancer neoantigen prioritization through sensitive and reliable proteogenomics analysis.

Nature Communications
Wen, Bo B; Li, Kai K; Zhang, Yun Y; Zhang, Bing B
Publication Date: 2020-04-09

Variant appearance in text: COMT: A72S
PubMed Link: 32273506
Variant Present in the following documents:
  • 41467_2020_15456_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Shared genetic susceptibilities for irritable bowel syndrome and depressive disorder in Chinese patients uncovered by pooled whole-exome sequencing.

Journal Of Advanced Research
Zhu, Shiwei S; He, Meibo M; Liu, Zuojing Z; Qin, Zelian Z; Wang, Zhiren Z; Duan, Liping L
Publication Date: 2020-05

Variant appearance in text: rs6267
PubMed Link: 32099673
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Biological Aspects of Aggression and Violence in Schizophrenia.

Clinical Psychopharmacology And Neuroscience : The Official Scientific Journal Of The Korean College Of Neuropsychopharmacology
Cho, WonKyung W; Shin, Won-Suk WS; An, Iseul I; Bang, Minji M; Cho, Doo-Yeoun DY; Lee, Sang-Hyuk SH
Publication Date: 2019-11-20

Variant appearance in text: COMT: Ala72Ser
PubMed Link: 31671484
Variant Present in the following documents:
  • Main text
  • cpn-17-475.pdf
View BVdb publication page



No association of COMT with insight problem solving in Chinese college students.

Peerj
Yang, Xiaolei X; Zhang, Jinghuan J; Zhang, Shun S
Publication Date: 2019

Variant appearance in text: rs6267
PubMed Link: 31024766
Variant Present in the following documents:
  • Main text
  • peerj-07-6755.pdf
View BVdb publication page



Catechol-O-methyltransferase polymorphism Val158Met is associated with distal neuropathic pain in HIV-associated sensory neuropathy.

Aids (London, England)
Xu, Jennie J; Umlauf, Anya A; Letendre, Scott S; Franklin, Donald D; Bush, William S WS; Atkinson, Joseph H JH; Keltner, John J; Ellis, Ronald J RJ
Publication Date: 2019-08-01

Variant appearance in text: rs6267
PubMed Link: 31021849
Variant Present in the following documents:
  • Main text
View BVdb publication page



A candidate gene study of risk for dementia in older, postmenopausal women: Results from the Women's Health Initiative Memory Study.

International Journal Of Geriatric Psychiatry
Driscoll, Ira I; Snively, Beverly M BM; Espeland, Mark A MA; Shumaker, Sally A SA; Rapp, Stephen R SR; Goveas, Joseph S JS; Casanova, Ramon L RL; Wactawski-Wende, Jean J; Manson, JoAnn E JE; Rossom, Rebecca R; Brooks, Janet J; Hernandez, Dena G DG; Singleton, Andrew B AB; Resnick, Susan M SM
Publication Date: 2019-05

Variant appearance in text: rs6267
PubMed Link: 30706571
Variant Present in the following documents:
  • Main text
View BVdb publication page



Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons.

Stem Cell Reports
Deneault, Eric E; White, Sean H SH; Rodrigues, Deivid C DC; Ross, P Joel PJ; Faheem, Muhammad M; Zaslavsky, Kirill K; Wang, Zhuozhi Z; Alexandrova, Roumiana R; Pellecchia, Giovanna G; Wei, Wei W; Piekna, Alina A; Kaur, Gaganjot G; Howe, Jennifer L JL; Kwan, Vickie V; Thiruvahindrapuram, Bhooma B; Walker, Susan S; Lionel, Anath C AC; Pasceri, Peter P; Merico, Daniele D; Yuen, Ryan K C RKC; Singh, Karun K KK; Ellis, James J; Scherer, Stephen W SW
Publication Date: 2018-11-13

Variant appearance in text: COMT: Ala72Ser
PubMed Link: 30392976
Variant Present in the following documents:
  • mmc5.pdf
View BVdb publication page



Development of an AmpliSeqTM Panel for Next-Generation Sequencing of a Set of Genetic Predictors of Persisting Pain.

Frontiers In Pharmacology
Kringel, Dario D; Kaunisto, Mari A MA; Lippmann, Catharina C; Kalso, Eija E; Lötsch, Jörn J
Publication Date: 2018

Variant appearance in text: rs6267
PubMed Link: 30283335
Variant Present in the following documents:
  • Main text
View BVdb publication page



A weighted burden test using logistic regression for integrated analysis of sequence variants, copy number variants and polygenic risk score.

European Journal Of Human Genetics : Ejhg
Curtis, David D
Publication Date: 2019-01

Variant appearance in text: rs6267
PubMed Link: 30258123
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations Between Gene Polymorphisms and Psychological Stress in the Guangxi Minority Region of China.

Medical Science Monitor : International Medical Journal Of Experimental And Clinical Research
Lin, Xiujin X; Liu, Jianbo J; Fu, Peipei P; Zeng, Xuan X; Qin, Jian J; Tang, Zhenghua Z; Wu, Junduan J
Publication Date: 2018-09-22

Variant appearance in text: rs6267
PubMed Link: 30242809
Variant Present in the following documents:
  • Main text
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs6267
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Interaction Between Environmental Risk Factors and Catechol-O-Methyltransferase (COMT) and X-Ray Repair Cross-Complementing Protein 1 (XRCC1) Gene Polymorphisms in Risk of Lung Cancer Among Non-Smoking Chinese Women: A Case-Control Study.

Medical Science Monitor : International Medical Journal Of Experimental And Clinical Research
Pan, Jian-Liang JL; Gao, Jin J; Hou, Jian-Hua JH; Hu, De-Zhong DZ; Li, Lin L
Publication Date: 2018-08-15

Variant appearance in text: COMT: Ala72Ser
PubMed Link: 30109864
Variant Present in the following documents:
  • Main text
View BVdb publication page



Interacting Effect of Catechol-O-Methyltransferase (COMT) and Monoamine Oxidase A (MAOA) Gene Polymorphisms, and Stressful Life Events on Aggressive Behavior in Chinese Male Adolescents.

Frontiers In Psychology
Wang, Meiping M; Li, Hailei H; Deater-Deckard, Kirby K; Zhang, Wenxin W
Publication Date: 2018

Variant appearance in text: COMT: Ala72Ser; rs6267
PubMed Link: 30018578
Variant Present in the following documents:
  • Main text
  • fpsyg-09-01079.pdf
View BVdb publication page



The Role of Genetic Polymorphisms in Chronic Pain Patients.

International Journal Of Molecular Sciences
Knezevic, Nebojsa Nick NN; Tverdohleb, Tatiana T; Knezevic, Ivana I; Candido, Kenneth D KD
Publication Date: 2018-06-08

Variant appearance in text: rs6267
PubMed Link: 29890676
Variant Present in the following documents:
  • Main text
  • ijms-19-01707.pdf
View BVdb publication page



Significance of neurexin and neuroligin polymorphisms in regulating risk of Hirschsprung's disease.

Journal Of Investigative Medicine : The Official Publication Of The American Federation For Clinical Research
Li, Yanhong Y; Liu, Hui H; Dong, Yubin Y
Publication Date: 2018-06

Variant appearance in text: rs6267
PubMed Link: 29622757
Variant Present in the following documents:
  • Main text
  • jim-2017-000623.pdf
View BVdb publication page



Weighted Burden Analysis of Exome-Sequenced Case-Control Sample Implicates Synaptic Genes in Schizophrenia Aetiology.

Behavior Genetics
Curtis, David D; Coelewij, Leda L; Liu, Shou-Hwa SH; Humphrey, Jack J; Mott, Richard R
Publication Date: 2018-05

Variant appearance in text: rs6267
PubMed Link: 29564678
Variant Present in the following documents:
  • Main text
  • 10519_2018_Article_9893.pdf
View BVdb publication page



Discovery of coding regions in the human genome by integrated proteogenomics analysis workflow.

Nature Communications
Zhu, Yafeng Y; Orre, Lukas M LM; Johansson, Henrik J HJ; Huss, Mikael M; Boekel, Jorrit J; Vesterlund, Mattias M; Fernandez-Woodbridge, Alejandro A; Branca, Rui M M RMM; Lehtiö, Janne J
Publication Date: 2018-03-02

Variant appearance in text: rs6267
PubMed Link: 29500430
Variant Present in the following documents:
  • 41467_2018_3311_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Genetic variation in human drug-related genes.

Genome Medicine
Schärfe, Charlotta Pauline Irmgard CPI; Tremmel, Roman R; Schwab, Matthias M; Kohlbacher, Oliver O; Marks, Debora Susan DS
Publication Date: 2017-12-22

Variant appearance in text: rs6267
PubMed Link: 29273096
Variant Present in the following documents:
  • 13073_2017_502_MOESM2_ESM.xlsx, sheet 2
View BVdb publication page



Depression and Catechol-O-methyltransferase (COMT) genetic variants are associated with pain in Parkinson's disease.

Scientific Reports
Lin, Chin-Hsien CH; Chaudhuri, K Ray KR; Fan, Jun-Yu JY; Ko, Chia-I CI; Rizos, Alexandra A; Chang, Chia-Wen CW; Lin, Han-I HI; Wu, Yih-Ru YR
Publication Date: 2017-07-24

Variant appearance in text: COMT: 214G>T; A72S; rs6267
PubMed Link: 28740224
Variant Present in the following documents:
  • Main text
  • 41598_2017_6782_MOESM1_ESM.pdf
  • 41598_2017_Article_6782.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: COMT: A72S; rs6267
PubMed Link: 28716134
Variant Present in the following documents:
  • 13073_2017_454_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: COMT: A72S; rs6267
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



Theranostic Biomarkers for Schizophrenia.

International Journal Of Molecular Sciences
Perkovic, Matea Nikolac MN; Erjavec, Gordana Nedic GN; Strac, Dubravka Svob DS; Uzun, Suzana S; Kozumplik, Oliver O; Pivac, Nela N
Publication Date: 2017-03-30

Variant appearance in text: COMT: Ala72Ser; rs6267
PubMed Link: 28358316
Variant Present in the following documents:
  • Main text
View BVdb publication page



Linkage and Association Analyses of Schizophrenia with Genetic Variations on Chromosome 22q11 in Koreans.

Psychiatry Investigation
Yoon, Se Chang SC; Jang, Yong Lee YL; Kim, Jong-Won JW; Cho, Eun-Young EY; Park, Dong Yeon DY; Hong, Kyung Sue KS; Lee, Yu Sang YS
Publication Date: 2016-11

Variant appearance in text: COMT: Ala72Ser
PubMed Link: 27909454
Variant Present in the following documents:
  • pi-13-630.pdf
View BVdb publication page