ClinVar Miner

List of variants in gene MFN2 reported as uncertain significance for Hereditary motor and sensory neuropathy with optic atrophy

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Total variants: 45
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HGVS dbSNP
NC_000001.11:g.11980166G>A
NM_001127660.1(MFN2):c.-214C>G
NM_001127660.1(MFN2):c.-237G>A
NM_014874.3(MFN2):c.*1068C>T rs886045229
NM_014874.3(MFN2):c.*1153C>T rs542684406
NM_014874.3(MFN2):c.*1276G>A rs766342161
NM_014874.3(MFN2):c.*1295G>A rs763783578
NM_014874.3(MFN2):c.*1392A>G rs886045230
NM_014874.3(MFN2):c.*1539G>A rs557643473
NM_014874.3(MFN2):c.*256G>A rs557772799
NM_014874.3(MFN2):c.*297T>A rs886045224
NM_014874.3(MFN2):c.*36G>A rs377468070
NM_014874.3(MFN2):c.*413C>T rs558887681
NM_014874.3(MFN2):c.*57C>T rs886045221
NM_014874.3(MFN2):c.*864T>C rs886045226
NM_014874.3(MFN2):c.*870C>T rs886045227
NM_014874.3(MFN2):c.*946C>A rs765105334
NM_014874.3(MFN2):c.-217C>A rs886045218
NM_014874.3(MFN2):c.-328T>A rs886045217
NM_014874.3(MFN2):c.-344C>T rs886045216
NM_014874.3(MFN2):c.1269G>A (p.Thr423=) rs145994616
NM_014874.3(MFN2):c.153G>T (p.Gln51His) rs886045219
NM_014874.3(MFN2):c.1659G>A (p.Val553=) rs886045220
NM_014874.3(MFN2):c.1858G>A (p.Val620Ile) rs200936779
NM_014874.3(MFN2):c.1946G>A (p.Arg649His) rs763492075
NM_014874.3(MFN2):c.1987C>T (p.Arg663Cys) rs369762154
NM_014874.3(MFN2):c.2157G>A (p.Lys719=) rs148441213
NM_014874.3(MFN2):c.756C>T (p.Asn252=) rs137960129
NM_014874.3(MFN2):c.842G>C (p.Cys281Ser) rs147136530
NM_014874.3(MFN2):c.898C>T (p.Arg300Cys) rs863224066
NM_014874.4(MFN2):c.*1054C>T
NM_014874.4(MFN2):c.*1222G>A
NM_014874.4(MFN2):c.*131G>A
NM_014874.4(MFN2):c.*1535C>T
NM_014874.4(MFN2):c.*1662T>C
NM_014874.4(MFN2):c.*1763G>A
NM_014874.4(MFN2):c.*1902C>T
NM_014874.4(MFN2):c.*381C>A
NM_014874.4(MFN2):c.*813G>A
NM_014874.4(MFN2):c.1631A>G (p.His544Arg)
NM_014874.4(MFN2):c.1716+8A>G
NM_014874.4(MFN2):c.1777T>A (p.Ser593Thr)
NM_014874.4(MFN2):c.1938C>A (p.Val646=)
NM_014874.4(MFN2):c.2211A>G (p.Lys737=)
NM_014874.4(MFN2):c.271G>A (p.Val91Met)

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