ClinVar Miner

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

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_000254.3(MTR):c.3711+194A>G rs201122094 0.03052
NM_000254.3(MTR):c.3711+196A>G rs202173360 0.02392
NM_000254.3(MTR):c.1515+103A>C rs73129143 0.02140
NM_000254.3(MTR):c.996-195A>G rs16834433 0.01684
NM_000254.3(MTR):c.2776-139C>T rs41295948 0.01605
NM_000254.3(MTR):c.1516-201G>A rs140704204 0.01222
NM_000254.3(MTR):c.1515+102C>T rs149779530 0.00933
NM_000254.3(MTR):c.1696-143T>C rs138667281 0.00928
NM_000254.3(MTR):c.765-82A>G rs75949532 0.00682
NM_000254.3(MTR):c.1516-83A>C rs560132465 0.00679
NM_000254.3(MTR):c.866-94T>C rs187490754 0.00506
NM_000254.3(MTR):c.2775+122A>G rs191779454 0.00494
NM_000254.3(MTR):c.2474-145_2474-144insT rs1189571643 0.00479
NM_000254.3(MTR):c.1075+130G>A rs114548075 0.00466
NM_000254.3(MTR):c.2474-17A>T rs571901048 0.00401
NM_000254.3(MTR):c.1076-8C>T rs115186224 0.00321
NM_000254.3(MTR):c.2406-106C>T rs114229303 0.00284
NM_000254.3(MTR):c.2349C>T (p.Asp783=) rs150734119 0.00261
NM_000254.3(MTR):c.2473+8G>T rs144061765 0.00260
NM_000254.3(MTR):c.764+16T>C rs138222686 0.00158
NM_000254.3(MTR):c.2622G>A (p.Pro874=) rs141919148 0.00064
NM_000254.3(MTR):c.1080A>G (p.Leu360=) rs141861479 0.00043
NM_000254.3(MTR):c.1977A>G (p.Lys659=) rs144767461 0.00038
NM_000254.3(MTR):c.3712-7T>G rs151081130 0.00036
NM_000254.3(MTR):c.1953+6G>C rs147410975 0.00034
NM_000254.3(MTR):c.3583A>G (p.Ile1195Val) rs149476106 0.00026
NM_000254.3(MTR):c.639T>C (p.Phe213=) rs568734591 0.00020
NM_000254.3(MTR):c.1075+7C>T rs202157685 0.00019
NM_000254.3(MTR):c.3405+18C>T rs374485228 0.00016
NM_000254.3(MTR):c.2043+10A>G rs375005444 0.00013
NM_000254.3(MTR):c.35-19A>G rs372886393 0.00013
NM_000254.3(MTR):c.3552C>T (p.Thr1184=) rs760793648 0.00010
NM_000254.3(MTR):c.3007+20C>A rs149877608 0.00009
NM_000254.3(MTR):c.2196+19G>T rs372533462 0.00008
NM_000254.3(MTR):c.3126C>T (p.Asp1042=) rs529430607 0.00008
NM_000254.3(MTR):c.3141C>T (p.Tyr1047=) rs560615373 0.00007
NM_000254.3(MTR):c.1076-11C>T rs186367553 0.00006
NM_000254.3(MTR):c.2994C>T (p.Asn998=) rs778549407 0.00005
NM_000254.3(MTR):c.764+6T>C rs377357761 0.00005
NM_000254.3(MTR):c.1086C>G (p.Pro362=) rs779393795 0.00004
NM_000254.3(MTR):c.1722T>C (p.Ser574=) rs142857114 0.00004
NM_000254.3(MTR):c.2703A>G (p.Leu901=) rs780615625 0.00004
NM_000254.3(MTR):c.2473+14A>G rs193210789 0.00003
NM_000254.3(MTR):c.3636T>C (p.Ala1212=) rs767100856 0.00003
NM_000254.3(MTR):c.1395G>A (p.Gly465=) rs372015549 0.00002
NM_000254.3(MTR):c.1953+7A>G rs777871271 0.00002
NM_000254.3(MTR):c.2772C>G (p.Leu924=) rs533541925 0.00002
NM_000254.3(MTR):c.2775+17G>T rs763995449 0.00002
NM_000254.3(MTR):c.2910G>A (p.Val970=) rs769690083 0.00002
NM_000254.3(MTR):c.486G>A (p.Pro162=) rs747494979 0.00002
NM_000254.3(MTR):c.108G>A (p.Gly36=) rs1057523951 0.00001
NM_000254.3(MTR):c.1743C>T (p.Ser581=) rs758784869 0.00001
NM_000254.3(MTR):c.181A>C (p.Arg61=) rs886046217 0.00001
NM_000254.3(MTR):c.3516C>T (p.Arg1172=) rs750050502 0.00001
NM_000254.3(MTR):c.609+1092G>A rs1057521391 0.00001
NM_000254.3(MTR):c.-16GAG[1] rs1064794430
NM_000254.3(MTR):c.1266A>G (p.Leu422=) rs984927112
NM_000254.3(MTR):c.2044-2A>T rs753703111
NM_000254.3(MTR):c.2474-19_2474-18del rs150727404
NM_000254.3(MTR):c.2474-20_2474-18del rs150727404
NM_000254.3(MTR):c.2474-4dup rs546254033
NM_000254.3(MTR):c.2474-5_2474-4dup rs546254033
NM_000254.3(MTR):c.3003A>T (p.Thr1001=) rs1057520933
NM_000254.3(MTR):c.3711+194_3711+195insTGCGCGCGCGCGCACGCGCGCG rs1553331097
NM_000254.3(MTR):c.3711+8A>C rs1057523709
NM_000254.3(MTR):c.409+15_409+17del rs750828089
NM_000254.3(MTR):c.609+10G>A rs956538334
NM_000254.3(MTR):c.765-5del rs1064795174

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