Specifications of the ACMG/AMP standards and guidelines for mitochondrial DNA variant interpretation.

Specifications of the ACMG/AMP standards and guidelines for mitochondrial DNA variant interpretation.
复制标题

DOI:
10.1002/humu.24107
复制
发表时间:
2020-12
期刊:
影响因子:
3.9
通讯作者:
Falk MJ
Falk MJ
中科院分区:
医学2区
文献类型:
--
作者:
McCormick EM;Lott MT;Dulik MC;Shen L;Attimonelli M;Vitale O;Karaa A;Bai R;Pineda-Alvarez DE;Singh LN;Stanley CM;Wong S;Bhardwaj A;Merkurjev D;Mao R;Sondheimer N;Zhang S;Procaccio V;Wallace DC;Gai X;Falk MJ

文献摘要

参考文献

被引文献

相似文献

Mitochondrial DNA (mtDNA) variant pathogenicity interpretation has special considerations given unique features of the mtDNA genome, including maternal inheritance, variant heteroplasmy, threshold effect, absence of splicing, and contextual effects of haplogroups. Currently there are insufficient standardized criteria for mtDNA variant assessment, which leads to inconsistencies in clinical variant pathogenicity reporting. An international working group of mtDNA experts was assembled within the Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium and obtained Expert Panel status from ClinGen. This group reviewed the 2015 American College of Medical Genetics (ACMG) and Association of Molecular Pathology (AMP) standards and guidelines that are widely used for clinical interpretation of DNA sequence variants and provided further specifications for additional and specific guidance related to mtDNA variant classification. These Expert Panel based consensus specifications allow for consistent consideration of the unique aspects of the mtDNA genome that directly influence variant assessment, including addressing mtDNA genome composition and structure, haplogroups and phylogeny, maternal inheritance, heteroplasmy, and functional analyses unique to mtDNA, as well specifications for utilization of mtDNA genomic databases and computational algorithms.
使用LOVD平台朝着mtDNA基因座特异性突变数据库。
DOI: 10.1002/humu.22118
发表时间: 2012-09
期刊: HUMAN MUTATION
影响因子: 3.9
作者:
Elson, Joanna L.;Sweeney, Mary G.;Procaccio, Vincent;Yarham, John W.;Salas, Antonio;Kong, Qing-Peng;van der Westhuizen, Francois H.;Pitceathly, Robert D. S.;Thorburn, David R.;Lott, Marie T.;Wallace, Douglas C.;Taylor, Robert W.;McFarland, Robert
通讯作者: McFarland, Robert
DOI: 10.1002/humu.1380060405
发表时间: 1995-01-01
期刊: HUMAN MUTATION
影响因子: 3.9
作者:
BROWN, MD;TORRONI, A;WALLACE, DC
通讯作者: WALLACE, DC
DOI: 10.1056/nejm198307213090304
发表时间: 1983-01-01
影响因子: 158.5
作者:
EGGER, J;WILSON, J
通讯作者: WILSON, J
DOI: 10.1186/s12859-016-1193-4
发表时间: 2016-11-08
期刊: BMC bioinformatics
影响因子: 3
作者:
Diroma MA;Lubisco P;Attimonelli M
通讯作者: Attimonelli M
DOI: 10.1186/1476-4598-3-30
发表时间: 2004-01-01
期刊: MOLECULAR CANCER
影响因子: 37.3
作者:
Aikhionbare, Felix O.;Khan, Masood;Go, Rodney
通讯作者: Go, Rodney