ClinVar Miner

List of variants in gene MTR reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
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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.*5535G>A rs16834541
NM_000254.2(MTR):c.-111C>T rs113809927
NM_000254.2(MTR):c.-151C>T rs41305572
NM_000254.2(MTR):c.-201C>G rs111840642
NM_000254.2(MTR):c.-67C>T rs3738547
NM_000254.2(MTR):c.250-7G>A rs184332230
NM_000254.2(MTR):c.340-6C>T rs7526063
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.3599-10C>A rs41530146
NM_000254.2(MTR):c.3665A>G (p.Asn1222Ser) rs61739582
NM_000254.2(MTR):c.858C>T (p.Pro286=) rs146019467
NM_000254.2(MTR):c.940G>A (p.Asp314Asn) rs2229274
NM_001291939.1(MTR):c.*5194_*5198AAAAC[3] rs141529013

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