ClinVar Miner

List of variants in gene DNM2 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_001005361.3(DNM2):c.2139T>C (p.Ala713=) rs2229920 0.30148
NM_001005361.3(DNM2):c.2543+7C>G rs201979143 0.00364
NM_001005361.3(DNM2):c.1545+14C>G rs114713494 0.00350
NM_001005361.3(DNM2):c.190G>A (p.Val64Ile) rs144250390 0.00243
NM_001005361.3(DNM2):c.1781+17C>A rs75344643 0.00220
NM_001005361.3(DNM2):c.1902C>T (p.Asn634=) rs2229919 0.00149
NM_001005361.3(DNM2):c.589+17G>T rs374377836 0.00028
NM_001005361.3(DNM2):c.958G>A (p.Asp320Asn) rs150613209 0.00026
NM_001005361.3(DNM2):c.1546-16C>T rs375554484 0.00022
NM_001005361.3(DNM2):c.882G>A (p.Pro294=) rs144790170 0.00018
NM_001005361.3(DNM2):c.789G>A (p.Pro263=) rs199976453 0.00014
NM_001005361.3(DNM2):c.822G>A (p.Thr274=) rs201763720 0.00014
NM_001005361.3(DNM2):c.1827C>T (p.Ser609=) rs371412466 0.00013
NM_001005361.3(DNM2):c.1422+9C>T rs199952853 0.00012
NM_001005361.3(DNM2):c.957C>T (p.Pro319=) rs141911457 0.00012
NM_001005361.3(DNM2):c.*14C>T rs369529119 0.00010
NM_001005361.3(DNM2):c.555C>T (p.Asp185=) rs140788791 0.00009
NM_001005361.3(DNM2):c.633C>T (p.Asp211=) rs200191870 0.00009
NM_001005361.3(DNM2):c.666C>T (p.Asn222=) rs2229921 0.00008
NM_001005361.3(DNM2):c.876G>A (p.Ser292=) rs749140605 0.00008
NM_001005361.3(DNM2):c.1196+778G>C rs763908447 0.00006
NM_001005361.3(DNM2):c.1449G>A (p.Gln483=) rs750299400 0.00006
NM_001005361.3(DNM2):c.1893+10C>T rs147321173 0.00006
NM_001005361.3(DNM2):c.450A>G (p.Pro150=) rs766121627 0.00006
NM_001005361.3(DNM2):c.1032C>T (p.Ile344=) rs747050783 0.00004
NM_001005361.3(DNM2):c.162-16T>C rs573469750 0.00004
NM_001005361.3(DNM2):c.1893+17C>T rs45585238 0.00004
NM_001005361.3(DNM2):c.2292-15T>A rs534518685 0.00004
NM_001005361.3(DNM2):c.993-14C>T rs761380478 0.00004
NM_001005361.3(DNM2):c.1518G>C (p.Leu506=) rs201426481 0.00003
NM_001005361.3(DNM2):c.2016C>T (p.Arg672=) rs368131004 0.00003
NM_001005361.3(DNM2):c.2031G>A (p.Lys677=) rs768285660 0.00003
NM_001005361.3(DNM2):c.471G>A (p.Lys157=) rs757708760 0.00003
NM_001005361.3(DNM2):c.992+11C>T rs761511769 0.00003
NM_001005361.3(DNM2):c.1071C>T (p.Ser357=) rs779241319 0.00001
NM_001005361.3(DNM2):c.1110C>T (p.Phe370=) rs201700534 0.00001
NM_001005361.3(DNM2):c.1128+13G>A rs772437963 0.00001
NM_001005361.3(DNM2):c.1423-4C>T rs552776205 0.00001
NM_001005361.3(DNM2):c.1494-19G>T rs1032876620 0.00001
NM_001005361.3(DNM2):c.162-6del rs766449694 0.00001
NM_001005361.3(DNM2):c.1758C>T (p.Phe586=) rs766274376 0.00001
NM_001005361.3(DNM2):c.183A>G (p.Ser61=) rs149555942 0.00001
NM_001005361.3(DNM2):c.1872C>T (p.Gly624=) rs774256221 0.00001
NM_001005361.3(DNM2):c.1894-9C>T rs377410182 0.00001
NM_001005361.3(DNM2):c.1973A>G (p.Asn658Ser) rs753175954 0.00001
NM_001005361.3(DNM2):c.2201A>G (p.Asn734Ser) rs577767034 0.00001
NM_001005361.3(DNM2):c.2391C>T (p.Pro797=) rs777834732 0.00001
NM_001005361.3(DNM2):c.2544-19G>A rs769617279 0.00001
NM_001005361.3(DNM2):c.402C>T (p.Leu134=) rs748069348 0.00001
NM_001005361.3(DNM2):c.858C>G (p.Thr286=) rs542637338 0.00001
NM_001005361.3(DNM2):c.1196+643C>T rs563985581
NM_001005361.3(DNM2):c.1493+16G>A rs1446097383
NM_001005361.3(DNM2):c.1545+11C>T rs1555712626
NM_001005361.3(DNM2):c.1546-18A>C rs1426762153
NM_001005361.3(DNM2):c.1557+9A>T rs778469445
NM_001005361.3(DNM2):c.1584C>T (p.Ile528=) rs935512495
NM_001005361.3(DNM2):c.162-9C>G rs200736669
NM_001005361.3(DNM2):c.1665T>C (p.Asp555=) rs1555713814
NM_001005361.3(DNM2):c.1782-4G>C rs767424969
NM_001005361.3(DNM2):c.1782-5del rs760441017
NM_001005361.3(DNM2):c.2256C>G (p.Val752=) rs751020224
NM_001005361.3(DNM2):c.2589A>C (p.Pro863=) rs1555717448
NM_001005361.3(DNM2):c.590-31CCTCTGA[3] rs748362325
NM_001005361.3(DNM2):c.688+15del rs1555706470
NM_001005361.3(DNM2):c.831G>A (p.Leu277=) rs1555707690

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