ClinVar Miner

List of variants in gene MTR reported as likely benign

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP
NM_000254.2(MTR):c.*1383C>T rs73131123
NM_000254.2(MTR):c.*1469T>C rs3768159
NM_000254.2(MTR):c.*1488T>C rs3768160
NM_000254.2(MTR):c.*153A>G rs11799670
NM_000254.2(MTR):c.*2388G>C rs78990641
NM_000254.2(MTR):c.*2879G>A rs74992803
NM_000254.2(MTR):c.*3140G>A rs3768161
NM_000254.2(MTR):c.*3174C>T rs41305961
NM_000254.2(MTR):c.*3322C>G rs76520920
NM_000254.2(MTR):c.*3464A>G rs61400757
NM_000254.2(MTR):c.*3601G>A rs59514993
NM_000254.2(MTR):c.*3683_*3684insTTAA rs149280661
NM_000254.2(MTR):c.*4065A>G rs6677090
NM_000254.2(MTR):c.*4461T>G rs113118968
NM_000254.2(MTR):c.*4776A>C rs79548228
NM_000254.2(MTR):c.*5170A>G rs6680753
NM_000254.2(MTR):c.*5194_*5198AAAAC[3] rs141529013
NM_000254.2(MTR):c.*5535G>A rs16834541
NM_000254.2(MTR):c.-111C>T rs113809927
NM_000254.2(MTR):c.-151C>T rs41305572
NM_000254.2(MTR):c.-16_-14GAG[1] rs1064794430
NM_000254.2(MTR):c.-201C>G rs111840642
NM_000254.2(MTR):c.-67C>T rs3738547
NM_000254.2(MTR):c.1033G>A (p.Val345Ile) rs145006491
NM_000254.2(MTR):c.1075+7C>T rs202157685
NM_000254.2(MTR):c.1076-11C>T rs186367553
NM_000254.2(MTR):c.1076-8C>T rs115186224
NM_000254.2(MTR):c.1080A>G (p.Leu360=) rs141861479
NM_000254.2(MTR):c.1086C>G (p.Pro362=) rs779393795
NM_000254.2(MTR):c.108G>A (p.Gly36=) rs1057523951
NM_000254.2(MTR):c.1266A>G (p.Leu422=) rs984927112
NM_000254.2(MTR):c.1395G>A (p.Gly465=) rs372015549
NM_000254.2(MTR):c.1722T>C (p.Ser574=) rs142857114
NM_000254.2(MTR):c.1743C>T (p.Ser581=)
NM_000254.2(MTR):c.181A>C (p.Arg61=) rs886046217
NM_000254.2(MTR):c.1953+6G>C rs147410975
NM_000254.2(MTR):c.1953+7A>G rs777871271
NM_000254.2(MTR):c.1977A>G (p.Lys659=) rs144767461
NM_000254.2(MTR):c.2043+10A>G rs375005444
NM_000254.2(MTR):c.2196+19G>T rs372533462
NM_000254.2(MTR):c.2349C>T (p.Asp783=) rs150734119
NM_000254.2(MTR):c.2473+14A>G rs193210789
NM_000254.2(MTR):c.2473+8G>T rs144061765
NM_000254.2(MTR):c.2474-4dupA rs546254033
NM_000254.2(MTR):c.250-7G>A rs184332230
NM_000254.2(MTR):c.2622G>A (p.Pro874=) rs141919148
NM_000254.2(MTR):c.2703A>G (p.Leu901=) rs780615625
NM_000254.2(MTR):c.2772C>G (p.Leu924=) rs533541925
NM_000254.2(MTR):c.2775+17G>T rs763995449
NM_000254.2(MTR):c.2815G>C (p.Gly939Arg) rs113042166
NM_000254.2(MTR):c.2910G>A (p.Val970=) rs769690083
NM_000254.2(MTR):c.2994C>T (p.Asn998=) rs778549407
NM_000254.2(MTR):c.3003A>T (p.Thr1001=) rs1057520933
NM_000254.2(MTR):c.3007+20C>A rs149877608
NM_000254.2(MTR):c.3126C>T (p.Asp1042=) rs529430607
NM_000254.2(MTR):c.3141C>T (p.Tyr1047=) rs560615373
NM_000254.2(MTR):c.34+10C>T rs376679817
NM_000254.2(MTR):c.340-6C>T rs7526063
NM_000254.2(MTR):c.3405+18C>T rs374485228
NM_000254.2(MTR):c.3477C>T (p.Asp1159=) rs117061132
NM_000254.2(MTR):c.3491G>A (p.Arg1164His) rs61736326
NM_000254.2(MTR):c.35-19A>G rs372886393
NM_000254.2(MTR):c.3516C>T (p.Arg1172=) rs750050502
NM_000254.2(MTR):c.3552C>T (p.Thr1184=) rs760793648
NM_000254.2(MTR):c.3583A>G (p.Ile1195Val) rs149476106
NM_000254.2(MTR):c.3599-10C>A rs41530146
NM_000254.2(MTR):c.3636T>C (p.Ala1212=) rs767100856
NM_000254.2(MTR):c.3665A>G (p.Asn1222Ser) rs61739582
NM_000254.2(MTR):c.3711+8A>C rs1057523709
NM_000254.2(MTR):c.3712-7T>G rs151081130
NM_000254.2(MTR):c.409+15_409+17delTCT rs750828089
NM_000254.2(MTR):c.486G>A (p.Pro162=) rs747494979
NM_000254.2(MTR):c.609+1092G>A rs1057521391
NM_000254.2(MTR):c.609+10G>A rs956538334
NM_000254.2(MTR):c.639T>C (p.Phe213=) rs568734591
NM_000254.2(MTR):c.669+20C>T rs200305844
NM_000254.2(MTR):c.764+16T>C rs138222686
NM_000254.2(MTR):c.764+6T>C rs377357761
NM_000254.2(MTR):c.765-5delT rs1064795174
NM_000254.2(MTR):c.858C>T (p.Pro286=) rs146019467
NM_000254.2(MTR):c.940G>A (p.Asp314Asn) rs2229274

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