ClinVar Miner

List of variants in gene MTRR reported as likely benign by GeneDx

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Gene type:
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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_002454.3(MTRR):c.1676+57C>T rs162052 0.02510
NM_002454.3(MTRR):c.1327+158A>G rs162043 0.02505
NM_002454.3(MTRR):c.1058-160A>G rs139816229 0.01796
NM_002454.3(MTRR):c.1370+69A>C rs79735541 0.01738
NM_002454.3(MTRR):c.1058-86C>A rs79408444 0.01737
NM_002454.3(MTRR):c.1952+176G>A rs41283147 0.01737
NM_002454.3(MTRR):c.1058-204T>C rs146422600 0.01709
NM_002454.3(MTRR):c.*151A>G rs112465197 0.01706
NM_002454.3(MTRR):c.781-291G>T rs6879300 0.01690
NM_002454.3(MTRR):c.1146+150G>A rs142261195 0.01605
NM_002454.3(MTRR):c.1953-124T>G rs142412032 0.01605
NM_002454.3(MTRR):c.*49A>G rs142538539 0.01601
NM_002454.3(MTRR):c.1371-245A>G rs141001076 0.01600
NM_002454.3(MTRR):c.129+152C>G rs7722483 0.01533
NM_002454.3(MTRR):c.130-272C>T rs114713553 0.01529
NM_002454.3(MTRR):c.1557+47T>G rs41282643 0.01142
NM_002454.3(MTRR):c.*167A>G rs115253331 0.01048
NC_000005.10:g.7869040G>A rs142579733 0.00577
NM_002454.3(MTRR):c.1676+137G>A rs73034455 0.00555
NM_002454.3(MTRR):c.903+265G>A rs184474926 0.00506
NM_002454.3(MTRR):c.288C>T (p.Leu96=) rs35587995 0.00500
NM_002454.3(MTRR):c.1057+22C>T rs114514595 0.00419
NM_002454.3(MTRR):c.1819G>A (p.Val607Ile) rs114259126 0.00366
NM_002454.3(MTRR):c.876C>T (p.Thr292=) rs144724549 0.00341
NM_002454.3(MTRR):c.284-34T>C rs147475536 0.00334
NM_002454.3(MTRR):c.210C>G (p.Arg70=) rs41282641 0.00303
NM_002454.3(MTRR):c.1982A>G (p.His661Arg) rs148909799 0.00196
NM_002454.3(MTRR):c.177C>G (p.Thr59=) rs142098262 0.00147
NM_002454.3(MTRR):c.1544C>T (p.Ala515Val) rs16879355 0.00145
NM_002454.3(MTRR):c.144C>T (p.Thr48=) rs138612190 0.00120
NM_002454.3(MTRR):c.828G>A (p.Val276=) rs115289458 0.00120
NM_002454.3(MTRR):c.781-14A>G rs112996747 0.00104
NM_002454.3(MTRR):c.54C>T (p.Ile18=) rs6413426 0.00062
NM_002454.3(MTRR):c.1770-42G>C rs2287781 0.00061
NM_002454.3(MTRR):c.540G>A (p.Val180=) rs149037732 0.00046
NM_002454.3(MTRR):c.463A>C (p.Arg155=) rs556611332 0.00016
NM_002454.3(MTRR):c.1020C>T (p.Cys340=) rs201348649 0.00010
NM_002454.3(MTRR):c.1058-17C>T rs754619256 0.00008
NM_002454.3(MTRR):c.1370+18C>T rs374485961 0.00006
NM_002454.3(MTRR):c.1147-16G>A rs143842562 0.00004
NM_002454.3(MTRR):c.402-19G>A rs192942300 0.00004
NM_002454.3(MTRR):c.1188T>C (p.Ala396=) rs763760088 0.00003
NM_002454.3(MTRR):c.129+16G>A rs1443181788 0.00003
NM_002454.3(MTRR):c.1575A>C (p.Arg525=) rs369430052 0.00002
NM_002454.3(MTRR):c.1641C>T (p.Thr547=) rs1044675786 0.00002
NM_002454.3(MTRR):c.1769+14C>T rs760216011 0.00002
NM_002454.3(MTRR):c.13C>T (p.Leu5=) rs763313419 0.00001
NM_002454.3(MTRR):c.2052C>T (p.Ala684=) rs1427160228 0.00001
NM_002454.3(MTRR):c.780+20T>C rs563392085 0.00001
NM_002454.3(MTRR):c.781-4C>G rs1057521905 0.00001
NM_002454.3(MTRR):c.1006A>G (p.Lys336Glu) rs1057521495
NM_002454.3(MTRR):c.1057+131A>G rs78869385
NM_002454.3(MTRR):c.1057+8C>G rs1325906968
NM_002454.3(MTRR):c.1676+86T>C rs6868871
NM_002454.3(MTRR):c.186C>T (p.Thr62=) rs940332374
NM_002454.3(MTRR):c.1875G>T (p.Val625=) rs12347
NM_002454.3(MTRR):c.1952+67G>C rs143443590
NM_002454.3(MTRR):c.75A>G (p.Gln25=) rs1553999358

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