ClinVar Miner

List of variants in gene combination LMNA, LOC126805877 reported as uncertain significance for Charcot-Marie-Tooth disease type 2

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Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_170707.4(LMNA):c.467G>A (p.Arg156His) rs764475194 0.00004
NM_170707.4(LMNA):c.364A>G (p.Lys122Glu) rs1222398892 0.00002
NM_170707.4(LMNA):c.439G>A (p.Ala147Thr) rs139875047 0.00001
NM_170707.4(LMNA):c.466C>T (p.Arg156Cys) rs760743233 0.00001
NM_170707.4(LMNA):c.478G>C (p.Gly160Arg) rs765665953 0.00001
NM_170707.4(LMNA):c.480C>T (p.Gly160=) rs758848135 0.00001
NM_170707.4(LMNA):c.504G>C (p.Gln168His) rs747771347 0.00001
NM_170707.4(LMNA):c.362C>T (p.Thr121Ile)
NM_170707.4(LMNA):c.364A>C (p.Lys122Gln) rs1222398892
NM_170707.4(LMNA):c.371A>G (p.Glu124Gly) rs1650969002
NM_170707.4(LMNA):c.376G>A (p.Asp126Asn) rs1351159308
NM_170707.4(LMNA):c.378C>A (p.Asp126Glu) rs869025456
NM_170707.4(LMNA):c.380T>C (p.Leu127Pro) rs2102865527
NM_170707.4(LMNA):c.388G>T (p.Ala130Ser) rs1650973752
NM_170707.4(LMNA):c.389C>A (p.Ala130Asp) rs1650973990
NM_170707.4(LMNA):c.393G>C (p.Gln131His) rs2102865651
NM_170707.4(LMNA):c.400C>G (p.Leu134Val) rs2527936107
NM_170707.4(LMNA):c.405_425dup (p.Leu141_Asn142insLysAspLeuGluAlaLeuLeu) rs2527936094
NM_170707.4(LMNA):c.409C>G (p.Leu137Val) rs747998566
NM_170707.4(LMNA):c.424A>G (p.Asn142Asp) rs1060502217
NM_170707.4(LMNA):c.430A>G (p.Lys144Glu) rs2102865891
NM_170707.4(LMNA):c.430_432del (p.Lys144del) rs1553264615
NM_170707.4(LMNA):c.431A>G (p.Lys144Arg) rs2527936480
NM_170707.4(LMNA):c.439G>C (p.Ala147Pro) rs139875047
NM_170707.4(LMNA):c.439G>T (p.Ala147Ser) rs139875047
NM_170707.4(LMNA):c.455T>C (p.Leu152Pro) rs2527936976
NM_170707.4(LMNA):c.460G>A (p.Glu154Lys) rs2527936999
NM_170707.4(LMNA):c.470C>G (p.Thr157Arg) rs754097769
NM_170707.4(LMNA):c.470C>T (p.Thr157Met) rs754097769
NM_170707.4(LMNA):c.471G>T (p.Thr157=) rs150645079
NM_170707.4(LMNA):c.475G>C (p.Glu159Gln) rs267607622
NM_170707.4(LMNA):c.489T>G (p.His163Gln) rs1558126350
NM_170707.4(LMNA):c.490G>A (p.Asp164Asn) rs751033102
NM_170707.4(LMNA):c.490G>T (p.Asp164Tyr) rs751033102
NM_170707.4(LMNA):c.491A>G (p.Asp164Gly) rs1650988739
NM_170707.4(LMNA):c.503A>G (p.Gln168Arg) rs1371187616
NM_170707.4(LMNA):c.507G>A (p.Val169=) rs2527938003
NM_170707.4(LMNA):c.511A>G (p.Lys171Glu) rs1650991296
NM_170707.4(LMNA):c.512A>G (p.Lys171Arg)
NM_170707.4(LMNA):c.513+45T>G rs878853220
NM_170707.4(LMNA):c.513+6G>A rs751256959
NM_170707.4(LMNA):c.513G>C (p.Lys171Asn) rs267607542

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