ClinVar Miner

List of variants in gene MTM1 reported as likely benign for not provided

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_000252.3(MTM1):c.1353+229A>G rs138203673 0.02531
NM_000252.3(MTM1):c.1260+134C>T rs144266984 0.01748
NM_000252.3(MTM1):c.343-100A>G rs222389 0.01524
NM_000252.3(MTM1):c.1353+262C>T rs111951773 0.01403
NM_000252.3(MTM1):c.1053+105A>C rs140153689 0.01044
NM_000252.3(MTM1):c.528+1035G>A rs140625961 0.01025
NM_000252.3(MTM1):c.-10-248C>T rs111468862 0.00734
NM_000252.3(MTM1):c.343-158A>G rs191242850 0.00706
NM_000252.3(MTM1):c.63+252C>T rs189339138 0.00636
NM_000252.3(MTM1):c.*182C>T rs222419 0.00587
NM_000252.3(MTM1):c.445-33C>T rs143521383 0.00507
NM_000252.3(MTM1):c.64-198A>G rs188412335 0.00482
NM_000252.3(MTM1):c.529-324G>A rs782664286 0.00390
NM_000252.3(MTM1):c.529-76G>A rs782310438 0.00367
NM_000252.3(MTM1):c.232-54A>T rs143312552 0.00356
NM_000252.3(MTM1):c.136+9C>T rs191553188 0.00337
NM_000252.3(MTM1):c.867+13A>C rs368954714 0.00051
NM_000252.3(MTM1):c.231+30C>A rs368915645 0.00010
NM_000252.3(MTM1):c.422C>T (p.Ala141Val) rs140642341 0.00007
NM_000252.3(MTM1):c.1080A>G (p.Val360=) rs782202285 0.00001
NM_000252.3(MTM1):c.136+172= rs222380
NM_000252.3(MTM1):c.343-192C>T rs7884615
NM_000252.3(MTM1):c.63+183dup rs1184716210
NM_000252.3(MTM1):c.679-150C>G rs113515087

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