ClinVar Miner

List of variants in gene DNM2 studied for not provided

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Gene type:
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Total variants: 84
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HGVS dbSNP
NM_001005360.2(DNM2):c.1004A>T (p.Gln335Leu) rs759996048
NM_001005360.2(DNM2):c.1051G>A (p.Val351Met) rs876661176
NM_001005360.2(DNM2):c.1070C>T (p.Ser357Phe) rs1064793101
NM_001005360.2(DNM2):c.1072G>A (p.Gly358Arg) rs267606772
NM_001005360.2(DNM2):c.1102G>A (p.Glu368Lys) rs121909092
NM_001005360.2(DNM2):c.1106G>T (p.Arg369Leu) rs121909089
NM_001005360.2(DNM2):c.1128+158G>C
NM_001005360.2(DNM2):c.1128+169T>C
NM_001005360.2(DNM2):c.1147G>T (p.Asp383Tyr) rs1568305190
NM_001005360.2(DNM2):c.1273C>A (p.Leu425Met) rs879253980
NM_001005360.2(DNM2):c.1335+241A>G
NM_001005360.2(DNM2):c.1335+939G>T
NM_001005360.2(DNM2):c.1336-196C>G
NM_001005360.2(DNM2):c.1352G>A (p.Arg451Gln) rs749154067
NM_001005360.2(DNM2):c.1370A>G (p.Glu457Gly) rs1555711301
NM_001005360.2(DNM2):c.1384A>G (p.Thr462Ala) rs201575500
NM_001005360.2(DNM2):c.1393C>T (p.Arg465Trp) rs121909091
NM_001005360.2(DNM2):c.1418A>T (p.Asp473Val) rs766613900
NM_001005360.2(DNM2):c.1423-9C>G rs371006369
NM_001005360.2(DNM2):c.1426C>A (p.Leu476Ile) rs1568309121
NM_001005360.2(DNM2):c.142C>T (p.Leu48=) rs753989925
NM_001005360.2(DNM2):c.1456A>G (p.Ile486Val) rs758246840
NM_001005360.2(DNM2):c.1494-43C>G
NM_001005360.2(DNM2):c.149A>G (p.Asn50Ser) rs757121012
NM_001005360.2(DNM2):c.1512G>A (p.Thr504=) rs767407905
NM_001005360.2(DNM2):c.1565G>A (p.Arg522His) rs587783595
NM_001005360.2(DNM2):c.1565G>T (p.Arg522Leu) rs587783595
NM_001005360.2(DNM2):c.1567A>G (p.Arg523Gly) rs587783596
NM_001005360.2(DNM2):c.1609G>A (p.Gly537Ser) rs121909093
NM_001005360.2(DNM2):c.161+122C>A
NM_001005360.2(DNM2):c.161+248G>C
NM_001005360.2(DNM2):c.1645T>A (p.Ser549Thr)
NM_001005360.2(DNM2):c.1676A>G (p.Lys559Arg) rs886043756
NM_001005360.2(DNM2):c.1678G>A (p.Glu560Lys) rs879254086
NM_001005360.2(DNM2):c.1747A>G (p.Lys583Glu) rs1568318798
NM_001005360.2(DNM2):c.1809C>G (p.Ile603Met) rs780409124
NM_001005360.2(DNM2):c.1836C>T (p.Asp612=) rs767061986
NM_001005360.2(DNM2):c.1852G>A (p.Ala618Thr) rs773598203
NM_001005360.2(DNM2):c.1856C>T (p.Ser619Leu) rs121909095
NM_001005360.2(DNM2):c.1872C>T (p.Gly624=) rs774256221
NM_001005360.2(DNM2):c.1879C>G (p.Pro627Ala) rs886039704
NM_001005360.2(DNM2):c.1880C>G (p.Pro627Arg) rs587783598
NM_001005360.2(DNM2):c.1893+18G>A
NM_001005360.2(DNM2):c.1893+248T>C
NM_001005360.2(DNM2):c.1894-181G>A
NM_001005360.2(DNM2):c.1902C>T (p.Asn634=) rs2229919
NM_001005360.2(DNM2):c.1903G>A (p.Glu635Lys) rs761198315
NM_001005360.2(DNM2):c.1912G>A (p.Ala638Thr) rs587778236
NM_001005360.2(DNM2):c.1934T>C (p.Met645Thr) rs879253969
NM_001005360.2(DNM2):c.1969C>T (p.Arg657Cys) rs772920450
NM_001005360.2(DNM2):c.1973A>G (p.Asn658Ser) rs753175954
NM_001005360.2(DNM2):c.2058+262A>G
NM_001005360.2(DNM2):c.2059-136G>C
NM_001005360.2(DNM2):c.216G>A (p.Gln72=) rs368075301
NM_001005360.2(DNM2):c.2201A>G (p.Asn734Ser) rs577767034
NM_001005360.2(DNM2):c.2231T>C (p.Val744Ala) rs777609224
NM_001005360.2(DNM2):c.2276G>A (p.Ser759Asn) rs879254300
NM_001005360.2(DNM2):c.2291+153G>A
NM_001005360.2(DNM2):c.235+10G>A rs769906659
NM_001005360.2(DNM2):c.235+12C>T
NM_001005360.2(DNM2):c.235+6A>G rs113192269
NM_001005360.2(DNM2):c.236-8C>G rs143084059
NM_001005360.2(DNM2):c.2365C>G (p.Pro789Ala) rs876661218
NM_001005360.2(DNM2):c.243C>T (p.Ala81=)
NM_001005360.2(DNM2):c.2484G>A (p.Pro828=) rs114682382
NM_001005360.2(DNM2):c.2543+7C>G rs201979143
NM_001005360.2(DNM2):c.2576_2581del (p.Thr859_Ile860del) rs876661117
NM_001005360.2(DNM2):c.2593G>A (p.Glu865Lys)
NM_001005360.2(DNM2):c.316G>A (p.Asp106Asn) rs375151459
NM_001005360.2(DNM2):c.385+60A>G
NM_001005360.2(DNM2):c.386-173G>T
NM_001005360.2(DNM2):c.386-6T>A rs114623441
NM_001005360.2(DNM2):c.590-168T>C
NM_001005360.2(DNM2):c.643G>A (p.Asp215Asn) rs145478270
NM_001005360.2(DNM2):c.645C>T (p.Asp215=) rs148900299
NM_001005360.2(DNM2):c.677C>T (p.Pro226Leu) rs779734638
NM_001005360.2(DNM2):c.736A>T (p.Lys246Ter) rs1555707649
NM_001005360.2(DNM2):c.839C>T (p.Thr280Met) rs202155679
NM_001005360.2(DNM2):c.868C>T (p.Arg290Trp) rs587778235
NM_001005360.2(DNM2):c.8A>G (p.Asn3Ser) rs890297188
NM_001005360.2(DNM2):c.953G>A (p.Arg318Gln) rs879254323
NM_001005360.2(DNM2):c.958G>A (p.Asp320Asn) rs150613209
NM_001005360.2(DNM2):c.992+231G>A
NM_001005360.2(DNM2):c.992A>G (p.Gln331Arg) rs879254084

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