ClinVar Miner

List of variants in gene MATR3 reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 90
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_199189.2(MATR3):c.-610C>G rs11242456 0.53822
NM_018834.6(MATR3):c.*1288T>G rs10515507 0.51394
NM_018834.6(MATR3):c.*672G>A rs7305 0.50625
NM_018834.6(MATR3):c.*1259G>C rs62381613 0.04668
NM_018834.6(MATR3):c.*177A>G rs13698 0.03913
NM_018834.6(MATR3):c.*708T>C rs14109 0.03387
NM_018834.6(MATR3):c.*1076T>C rs2015602 0.02638
NM_018834.6(MATR3):c.*1278T>C rs116341961 0.01780
NM_018834.6(MATR3):c.1602+6A>G rs80036770 0.01434
NM_018834.6(MATR3):c.*1535A>G rs111689401 0.01322
NM_018834.6(MATR3):c.-56G>A rs59033177 0.01187
NM_018834.6(MATR3):c.*1425C>G rs145516036 0.01098
NM_018834.6(MATR3):c.*1482A>T rs79616595 0.00669
NM_018834.6(MATR3):c.*1087G>C rs116660718 0.00535
NM_018834.6(MATR3):c.*275C>T rs187985845 0.00426
NM_018834.6(MATR3):c.*496C>T rs140707719 0.00411
NM_018834.6(MATR3):c.*747G>C rs181792838 0.00392
NM_018834.6(MATR3):c.*313A>G rs180806333 0.00300
NM_018834.6(MATR3):c.*1394G>A rs572983701 0.00217
NM_018834.6(MATR3):c.1347C>T (p.Ala449=) rs141986556 0.00120
NM_018834.6(MATR3):c.*1767C>T rs181125183 0.00104
NM_018834.6(MATR3):c.2360A>G (p.Asn787Ser) rs148402819 0.00083
NM_018834.6(MATR3):c.*769G>A rs561705958 0.00070
NM_018834.6(MATR3):c.*1757T>C rs191196444 0.00057
NM_199189.2(MATR3):c.-649C>T rs779721416 0.00053
NM_018834.6(MATR3):c.*2054T>A rs116278472 0.00047
NM_018834.6(MATR3):c.*2200C>T rs770043950 0.00043
NM_018834.6(MATR3):c.291A>G (p.Leu97=) rs147239107 0.00034
NM_018834.6(MATR3):c.1183-5G>A rs369464069 0.00028
NM_018834.6(MATR3):c.2521C>T (p.Arg841Cys) rs781050726 0.00022
NM_018834.6(MATR3):c.1132G>A (p.Ala378Thr) rs201075828 0.00017
NM_018834.6(MATR3):c.2504A>G (p.Asn835Ser) rs201165929 0.00015
NM_018834.6(MATR3):c.2283C>T (p.Asn761=) rs189752689 0.00014
NM_018834.6(MATR3):c.*2174C>T rs775200100 0.00011
NM_018834.6(MATR3):c.*857C>T rs745417770 0.00009
NM_018834.6(MATR3):c.2543A>G (p.Ter848=) rs200664940 0.00009
NM_018834.6(MATR3):c.*2241A>G rs886060006 0.00006
NM_018834.6(MATR3):c.*406A>G rs185734839 0.00006
NM_018834.6(MATR3):c.*2098A>G rs774066454 0.00004
NM_018834.6(MATR3):c.2191T>C (p.Leu731=) rs149714542 0.00004
NM_018834.6(MATR3):c.*1239A>G rs746298588 0.00003
NM_018834.6(MATR3):c.*2171C>T rs886060004 0.00003
NM_018834.6(MATR3):c.*2222G>T rs886060005 0.00003
NM_018834.6(MATR3):c.*587A>G rs535027907 0.00003
NM_018834.6(MATR3):c.*770A>G rs886059996 0.00003
NM_018834.6(MATR3):c.2494-14C>A rs779597861 0.00003
NM_199189.2(MATR3):c.-643A>G rs765907489 0.00003
NM_018834.6(MATR3):c.*1143G>A rs1357784533 0.00002
NM_018834.6(MATR3):c.*2170T>G rs1403800962 0.00002
NM_018834.6(MATR3):c.*262A>G rs1378690022 0.00002
NM_018834.6(MATR3):c.2242T>C (p.Ser748Pro) rs772562504 0.00002
NM_018834.6(MATR3):c.69G>A (p.Ala23=) rs750693851 0.00002
NM_018834.6(MATR3):c.*1111T>C rs772678059 0.00001
NM_018834.6(MATR3):c.*1891T>G rs886060001 0.00001
NM_018834.6(MATR3):c.*2142G>A rs1561950387 0.00001
NM_018834.6(MATR3):c.*2194T>A rs760576225 0.00001
NM_018834.6(MATR3):c.*305A>C rs563125595 0.00001
NM_018834.6(MATR3):c.*493T>C rs972728364 0.00001
NM_018834.6(MATR3):c.*60A>G rs886059993 0.00001
NM_018834.6(MATR3):c.*97C>G rs769044248 0.00001
NM_018834.6(MATR3):c.-5C>G rs375381025 0.00001
NM_018834.6(MATR3):c.1179A>G (p.Arg393=) rs747566193 0.00001
NM_018834.6(MATR3):c.1235G>A (p.Arg412Lys) rs1291862870 0.00001
NM_018834.6(MATR3):c.15C>T (p.Phe5=) rs184609870 0.00001
NM_018834.6(MATR3):c.2271T>C (p.Asp757=) rs753870064 0.00001
NM_018834.6(MATR3):c.305G>A (p.Arg102His) rs886059988 0.00001
NM_018834.6(MATR3):c.393C>A (p.Asp131Glu) rs761842979 0.00001
NM_018834.6(MATR3):c.*138T>C rs1756028343
NM_018834.6(MATR3):c.*1633T>C rs886059998
NM_018834.6(MATR3):c.*175AT[1] rs767576295
NM_018834.6(MATR3):c.*1810_*1812del rs144802057
NM_018834.6(MATR3):c.*1821T>G rs886060000
NM_018834.6(MATR3):c.*1999G>T rs886060002
NM_018834.6(MATR3):c.*2077A>C rs886060003
NM_018834.6(MATR3):c.*413A>T rs886059995
NM_018834.6(MATR3):c.*441C>G rs572126808
NM_018834.6(MATR3):c.*487C>T rs1756049111
NM_018834.6(MATR3):c.*640A>G rs145836548
NM_018834.6(MATR3):c.*86_*89del rs368308621
NM_018834.6(MATR3):c.*929G>A rs886059997
NM_018834.6(MATR3):c.-103dup rs59150359
NM_018834.6(MATR3):c.-124T>C rs886059987
NM_018834.6(MATR3):c.-139G>A rs886059986
NM_018834.6(MATR3):c.-43T>A rs12153162
NM_018834.6(MATR3):c.1734+11T>G rs886059990
NM_018834.6(MATR3):c.2233G>C (p.Ala745Pro) rs772433814
NM_018834.6(MATR3):c.2318A>G (p.Tyr773Cys) rs368217486
NM_018834.6(MATR3):c.2493+7_2493+9del rs886059992
NM_018834.6(MATR3):c.675A>G (p.Arg225=) rs199711502
NM_199189.2(MATR3):c.-563T>C rs1753162477

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.