ClinVar Miner

List of variants in gene DYSF reported as benign for not specified

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Total variants: 78
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HGVS dbSNP
NM_001130987.1(DYSF):c.460+2T>G rs750356247
NM_003494.3(DYSF):c.-34G>T rs192358316
NM_003494.3(DYSF):c.1038T>C (p.Pro346=) rs571559303
NM_003494.3(DYSF):c.1049C>T (p.Ala350Val) rs115279465
NM_003494.3(DYSF):c.1120G>C (p.Val374Leu) rs150724610
NM_003494.3(DYSF):c.1180+11C>T rs35982795
NM_003494.3(DYSF):c.1181-48A>G rs4852800
NM_003494.3(DYSF):c.1284+6G>C rs75796187
NM_003494.3(DYSF):c.1353+13C>T rs4852801
NM_003494.3(DYSF):c.1369G>A (p.Glu457Lys) rs61740288
NM_003494.3(DYSF):c.1422C>T (p.Ile474=) rs34387018
NM_003494.3(DYSF):c.1522+15C>G rs76402294
NM_003494.3(DYSF):c.1572C>T (p.Asn524=) rs139495331
NM_003494.3(DYSF):c.1731G>A (p.Ala577=) rs35984374
NM_003494.3(DYSF):c.1753-24C>G rs2303595
NM_003494.3(DYSF):c.1827T>C (p.Asp609=) rs2303596
NM_003494.3(DYSF):c.1860C>T (p.Tyr620=) rs35721373
NM_003494.3(DYSF):c.1890G>A (p.Pro630=) rs115849497
NM_003494.3(DYSF):c.1931-31C>A rs13424178
NM_003494.3(DYSF):c.2053C>G (p.Leu685Val) rs74423119
NM_003494.3(DYSF):c.2056-43G>T rs72827543
NM_003494.3(DYSF):c.2162+16C>T rs111389127
NM_003494.3(DYSF):c.2280C>T (p.Leu760=) rs116204385
NM_003494.3(DYSF):c.236+20G>A rs12470028
NM_003494.3(DYSF):c.236+31C>G rs78958249
NM_003494.3(DYSF):c.2367C>T (p.Ser789=) rs560856407
NM_003494.3(DYSF):c.2500A>G (p.Ile834Val) rs34671418
NM_003494.3(DYSF):c.2583A>T (p.Ser861=) rs2288355
NM_003494.3(DYSF):c.2588A>C (p.Asp863Ala) rs35884879
NM_003494.3(DYSF):c.2763G>A (p.Ser921=) rs148902254
NM_003494.3(DYSF):c.2802G>A (p.Pro934=) rs34836829
NM_003494.3(DYSF):c.3032-17G>A rs3764971
NM_003494.3(DYSF):c.3065G>A (p.Arg1022Gln) rs34211915
NM_003494.3(DYSF):c.3191_3196dupCGGAGG (p.Glu1065_Gly1066insAlaGlu) rs398123779
NM_003494.3(DYSF):c.3283C>T (p.Arg1095Cys) rs141536854
NM_003494.3(DYSF):c.3287G>A (p.Arg1096His) rs59915619
NM_003494.3(DYSF):c.3349-10G>A rs116733194
NM_003494.3(DYSF):c.3521-17C>T rs13421969
NM_003494.3(DYSF):c.3534C>T (p.Ile1178=) rs79899601
NM_003494.3(DYSF):c.3703-12C>T rs114968209
NM_003494.3(DYSF):c.383G>A (p.Gly128Glu) rs34997054
NM_003494.3(DYSF):c.3892A>G (p.Ile1298Val) rs121908954
NM_003494.3(DYSF):c.3914C>A (p.Thr1305Lys) rs116426399
NM_003494.3(DYSF):c.393C>T (p.Pro131=) rs34603128
NM_003494.3(DYSF):c.3972C>T (p.Asn1324=) rs11558179
NM_003494.3(DYSF):c.3992G>T (p.Arg1331Leu) rs61742872
NM_003494.3(DYSF):c.4006-40C>T rs2303605
NM_003494.3(DYSF):c.4008C>A (p.Ile1336=) rs2303606
NM_003494.3(DYSF):c.4068C>T (p.Ser1356=) rs2303607
NM_003494.3(DYSF):c.4168-20G>A rs111935215
NM_003494.3(DYSF):c.426C>T (p.Ser142=) rs115390288
NM_003494.3(DYSF):c.4323G>A (p.Gln1441=) rs76576806
NM_003494.3(DYSF):c.4374C>T (p.Ile1458=) rs145690047
NM_003494.3(DYSF):c.4376A>G (p.Asp1459Gly) rs61738567
NM_003494.3(DYSF):c.4443C>T (p.Phe1481=) rs544993852
NM_003494.3(DYSF):c.4504C>T (p.Leu1502=) rs7573406
NM_003494.3(DYSF):c.4509+43A>G rs84182
NM_003494.3(DYSF):c.457+17G>C rs115170960
NM_003494.3(DYSF):c.4731G>A (p.Glu1577=) rs62145939
NM_003494.3(DYSF):c.4820T>C (p.Ile1607Thr) rs146384562
NM_003494.3(DYSF):c.4887-37C>T rs2303599
NM_003494.3(DYSF):c.509C>A (p.Ala170Glu) rs34999029
NM_003494.3(DYSF):c.509C>T (p.Ala170Val) rs34999029
NM_003494.3(DYSF):c.5626G>A (p.Asp1876Asn) rs115013641
NM_003494.3(DYSF):c.565C>G (p.Leu189Val) rs13407355
NM_003494.3(DYSF):c.5668-41C>T rs2559081
NM_003494.3(DYSF):c.570T>C (p.Pro190=) rs35392229
NM_003494.3(DYSF):c.5768-16T>C rs1863812
NM_003494.3(DYSF):c.5859A>C (p.Pro1953=) rs17718530
NM_003494.3(DYSF):c.6063C>T (p.Pro2021=) rs147263499
NM_003494.3(DYSF):c.6204+15C>T rs2559082
NM_003494.3(DYSF):c.664-17C>T rs61104194
NM_003494.3(DYSF):c.681C>T (p.Ile227=) rs138054675
NM_003494.3(DYSF):c.792+11T>C rs13428076
NM_003494.3(DYSF):c.855+39T>C rs74384941
NM_003494.3(DYSF):c.855+4T>C rs11903960
NM_003494.3(DYSF):c.938-20G>A rs12713756
NM_003494.3(DYSF):c.942C>T (p.His314=) rs36122356

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