ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 90
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HGVS dbSNP gnomAD frequency
NM_002444.3(MSN):c.96+7C>T rs372696816 0.00042
NM_002444.3(MSN):c.429G>A (p.Lys143=) rs146058241 0.00022
NM_002444.3(MSN):c.1674C>T (p.Thr558=) rs1198738550 0.00007
NM_002444.3(MSN):c.960-4C>T rs755991085 0.00005
NM_002444.3(MSN):c.23G>A (p.Arg8His) rs200284989 0.00004
NM_002444.3(MSN):c.609G>A (p.Val203=) rs1052059259 0.00004
NM_002444.3(MSN):c.1091-18C>G rs769501693 0.00003
NM_002444.3(MSN):c.1108C>T (p.Arg370Cys) rs761864712 0.00002
NM_002444.3(MSN):c.1716C>T (p.Asp572=) rs756544101 0.00002
NM_002444.3(MSN):c.444C>T (p.Ala148=) rs368950777 0.00002
NM_002444.3(MSN):c.445G>A (p.Gly149Arg) rs757131925 0.00002
NM_002444.3(MSN):c.1095G>A (p.Leu365=) rs1377591899 0.00001
NM_002444.3(MSN):c.1539G>A (p.Glu513=) rs760128200 0.00001
NM_002444.3(MSN):c.1569+8A>C rs1230800513 0.00001
NM_002444.3(MSN):c.193-14C>T rs1215122427 0.00001
NM_002444.3(MSN):c.373C>T (p.Leu125=) rs768921044 0.00001
NM_002444.3(MSN):c.1062C>T (p.Ile354=)
NM_002444.3(MSN):c.1063G>A (p.Glu355Lys)
NM_002444.3(MSN):c.1091-13C>T
NM_002444.3(MSN):c.1091-8C>T
NM_002444.3(MSN):c.1119G>A (p.Leu373=)
NM_002444.3(MSN):c.1191A>G (p.Glu397=)
NM_002444.3(MSN):c.12+10G>A
NM_002444.3(MSN):c.12+11del
NM_002444.3(MSN):c.12+17_12+18insC
NM_002444.3(MSN):c.1222C>T (p.Arg408Trp) rs748200741
NM_002444.3(MSN):c.1224G>A (p.Arg408=)
NM_002444.3(MSN):c.123A>G (p.Glu41=)
NM_002444.3(MSN):c.1245A>G (p.Glu415=)
NM_002444.3(MSN):c.1251+14G>A
NM_002444.3(MSN):c.1252-8A>T rs2071702740
NM_002444.3(MSN):c.1254C>T (p.Ala418=)
NM_002444.3(MSN):c.1257G>A (p.Leu419=)
NM_002444.3(MSN):c.13-10C>A
NM_002444.3(MSN):c.1344+11G>A
NM_002444.3(MSN):c.1344+17A>C
NM_002444.3(MSN):c.1344+20G>A
NM_002444.3(MSN):c.1344+7C>G
NM_002444.3(MSN):c.1344+7C>T
NM_002444.3(MSN):c.1479C>T (p.Asp493=)
NM_002444.3(MSN):c.1545T>C (p.Asn515=)
NM_002444.3(MSN):c.1569+16C>T
NM_002444.3(MSN):c.1570-7C>A
NM_002444.3(MSN):c.1587G>A (p.Leu529=)
NM_002444.3(MSN):c.1680C>T (p.Arg560=) rs2147521386
NM_002444.3(MSN):c.171C>T (p.Thr57=) rs2147509954
NM_002444.3(MSN):c.193-20A>C
NM_002444.3(MSN):c.242G>A (p.Arg81His)
NM_002444.3(MSN):c.246C>G (p.Ala82=) rs2147511555
NM_002444.3(MSN):c.258T>G (p.Pro86=)
NM_002444.3(MSN):c.270C>T (p.Ser90=)
NM_002444.3(MSN):c.318G>C (p.Val106=)
NM_002444.3(MSN):c.333C>G (p.Leu111=)
NM_002444.3(MSN):c.333C>T (p.Leu111=)
NM_002444.3(MSN):c.342T>C (p.Asp114=)
NM_002444.3(MSN):c.363C>T (p.Thr121=)
NM_002444.3(MSN):c.406G>A (p.Asp136Asn)
NM_002444.3(MSN):c.443C>T (p.Ala148Val)
NM_002444.3(MSN):c.462G>A (p.Pro154=)
NM_002444.3(MSN):c.468-14C>T
NM_002444.3(MSN):c.468-20A>G rs2147513014
NM_002444.3(MSN):c.489C>G (p.Leu163=)
NM_002444.3(MSN):c.537C>T (p.His179=)
NM_002444.3(MSN):c.552-10T>C
NM_002444.3(MSN):c.588A>G (p.Gln196=)
NM_002444.3(MSN):c.60C>T (p.Ile20=)
NM_002444.3(MSN):c.639C>T (p.Gly213=)
NM_002444.3(MSN):c.657G>C (p.Gly219=) rs2071626634
NM_002444.3(MSN):c.699-18T>C
NM_002444.3(MSN):c.705T>C (p.Thr235=)
NM_002444.3(MSN):c.72C>A (p.Thr24=)
NM_002444.3(MSN):c.75C>G (p.Thr25=)
NM_002444.3(MSN):c.768C>A (p.Val256=)
NM_002444.3(MSN):c.783C>T (p.Asp261=)
NM_002444.3(MSN):c.78G>A (p.Gly26=)
NM_002444.3(MSN):c.795+10T>A rs983414758
NM_002444.3(MSN):c.795+14C>T
NM_002444.3(MSN):c.795+16C>T
NM_002444.3(MSN):c.796-15C>T
NM_002444.3(MSN):c.796-6C>T
NM_002444.3(MSN):c.846C>G (p.Ala282=)
NM_002444.3(MSN):c.846C>T (p.Ala282=)
NM_002444.3(MSN):c.870A>G (p.Leu290=)
NM_002444.3(MSN):c.894T>C (p.Asp298=)
NM_002444.3(MSN):c.897C>T (p.Thr299=)
NM_002444.3(MSN):c.906G>A (p.Val302=) rs2147516956
NM_002444.3(MSN):c.93C>T (p.Asp31=)
NM_002444.3(MSN):c.96+8G>A
NM_002444.3(MSN):c.969G>A (p.Leu323=)
NM_002444.3(MSN):c.975T>C (p.Asn325=)

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