Literature DB >> 27822869

Describing Sequence Variants Using HGVS Nomenclature.

Johan T den Dunnen1,2.   

Abstract

DNA sequencing is usually performed to determine the sequence of a region of interest or even the entire genome of an individual. After sequencing, the sequence obtained is compared to a reference, all differences (the variants) are recorded, and the possible consequences of the changes identified, on both the RNA and protein level, are predicted. Finally, when available, a database containing previously reported variants is consulted to determine what other studies might have revealed about the variant or other variants in the same sequence (gene) and what the functional and phenotypic consequences were for the individuals carrying the variant.To facilitate the reporting and databasing of variants a standard was developed, the HGVS recommendations for the description of sequence variants. HGVS nomenclature contains specific formats to describe the basic variant types; substitution, deletion, duplication, insertion, inversion, and conversion. The basics of how to apply the recommendations to describe sequence variants will be explained here. An extensive description of the current HGVS guidelines (version 15.11) is available online at http://www.HGVS.org/varnomen .

Keywords:  DNA; Database; Mutation; Nomenclature; Protein; RNA; Standards; Variant

Mesh:

Year:  2017        PMID: 27822869     DOI: 10.1007/978-1-4939-6442-0_17

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  11 in total

1.  MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.

Authors:  Julia Wang; Rami Al-Ouran; Yanhui Hu; Seon-Young Kim; Ying-Wooi Wan; Michael F Wangler; Shinya Yamamoto; Hsiao-Tuan Chao; Aram Comjean; Stephanie E Mohr; Norbert Perrimon; Zhandong Liu; Hugo J Bellen
Journal:  Am J Hum Genet       Date:  2017-05-11       Impact factor: 11.025

Review 2.  Morphomechanic phenotypic variability of sarcomeric cardiomyopathies: A multifactorial polygenic perspective.

Authors:  Ares Pasipoularides
Journal:  J Mol Cell Cardiol       Date:  2018-11-10       Impact factor: 5.000

3.  Long-term neurodevelopmental outcomes of hematopoietic stem cell transplantation for late-infantile Krabbe disease.

Authors:  Isabel C Yoon; Nicholas A Bascou; Michele D Poe; Paul Szabolcs; Maria L Escolar
Journal:  Blood       Date:  2021-04-01       Impact factor: 22.113

4.  Variant type and position predict two distinct limb phenotypes in patients with GLI3-mediated polydactyly syndromes.

Authors:  Martijn Baas; Elise Bette Burger; Ans Mw van den Ouweland; Steven Er Hovius; Annelies de Klein; Christianne A van Nieuwenhoven; Robert Jan H Galjaard
Journal:  J Med Genet       Date:  2020-06-26       Impact factor: 6.318

5.  GenProBiS: web server for mapping of sequence variants to protein binding sites.

Authors:  Janez Konc; Blaz Skrlj; Nika Erzen; Tanja Kunej; Dusanka Janezic
Journal:  Nucleic Acids Res       Date:  2017-07-03       Impact factor: 16.971

6.  Distinct diagnostic trajectories in NBAS-associated acute liver failure highlights the need for timely functional studies.

Authors:  Lauren S Akesson; Rocio Rius; Natasha J Brown; Jeremy Rosenbaum; Sarah Donoghue; Michael Stormon; Charmaine Chai; Esmeralda Bordador; Yiran Guo; Hakon Hakonarson; Alison G Compton; David R Thorburn; Sumudu Amarasekera; Justine Marum; Alisha Monaco; Crystle Lee; Belinda Chong; Sebastian Lunke; Zornitza Stark; John Christodoulou
Journal:  JIMD Rep       Date:  2022-03-15

7.  A prospective natural history study of Krabbe disease in a patient cohort with onset between 6 months and 3 years of life.

Authors:  Nicholas Bascou; Anthony DeRenzo; Michele D Poe; Maria L Escolar
Journal:  Orphanet J Rare Dis       Date:  2018-08-09       Impact factor: 4.123

8.  Heteroplasmic Variants of Mitochondrial DNA in Atherosclerotic Lesions of Human Aortic Intima.

Authors:  Igor A Sobenin; Andrey V Zhelankin; Zukhra B Khasanova; Vasily V Sinyov; Lyudmila V Medvedeva; Maria O Sagaidak; Vsevolod J Makeev; Kira I Kolmychkova; Anna S Smirnova; Vasily N Sukhorukov; Anton Y Postnov; Andrey V Grechko; Alexander N Orekhov
Journal:  Biomolecules       Date:  2019-09-06

9.  Misannotation of multiple-nucleotide variants risks misdiagnosis.

Authors:  Matthew N Wakeling; Thomas W Laver; Kevin Colclough; Andrew Parish; Sian Ellard; Emma L Baple
Journal:  Wellcome Open Res       Date:  2019-10-01

10.  Recommendations for the collection and use of multiplexed functional data for clinical variant interpretation.

Authors:  Hannah Gelman; Jennifer N Dines; Jonathan Berg; Alice H Berger; Sarah Brnich; Fuki M Hisama; Richard G James; Alan F Rubin; Jay Shendure; Brian Shirts; Douglas M Fowler; Lea M Starita
Journal:  Genome Med       Date:  2019-12-20       Impact factor: 11.117

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.