ClinVar Miner

List of variants in gene DNM1 reported as benign by Invitae

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Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_004408.4(DNM1):c.1008C>T (p.Phe336=) rs3003609 0.41986
NM_004408.4(DNM1):c.1062C>T (p.Tyr354=) rs35048348 0.08186
NM_004408.4(DNM1):c.1905+17C>T rs115623280 0.00965
NM_004408.4(DNM1):c.1894-18G>T rs116335289 0.00963
NM_004408.4(DNM1):c.1197-7C>T rs41306488 0.00247
NM_004408.4(DNM1):c.1906-17T>C rs191460911 0.00225
NM_004408.4(DNM1):c.1764C>T (p.Leu588=) rs111534551 0.00186
NM_004408.4(DNM1):c.1782-9A>G rs201739236 0.00090
NM_004408.4(DNM1):c.747C>T (p.Thr249=) rs141651183 0.00086
NM_004408.4(DNM1):c.2540C>T (p.Ser847Leu) rs199498658 0.00076
NM_004408.4(DNM1):c.1437C>T (p.Ile479=) rs141788807 0.00036
NM_004408.4(DNM1):c.849+6C>T rs527412689 0.00013
NM_004408.4(DNM1):c.2541G>A (p.Ser847=) rs545142847 0.00007
NM_004408.4(DNM1):c.1422+6C>T rs773817727 0.00005
NM_004408.4(DNM1):c.1128+11C>G rs761415279 0.00004
NM_004408.4(DNM1):c.1401C>T (p.Arg467=) rs527820256 0.00002
NM_004408.4(DNM1):c.1662G>A (p.Lys554=) rs371589347 0.00002
NM_004408.4(DNM1):c.1886G>A (p.Arg629His) rs778378392 0.00002
NM_004408.4(DNM1):c.1933G>A (p.Asp645Asn) rs754501788 0.00002
NM_004408.4(DNM1):c.1196+4C>T rs1445161696 0.00001
NM_004408.4(DNM1):c.1298C>T (p.Ser433Leu) rs762000203 0.00001
NM_004408.4(DNM1):c.1330A>G (p.Lys444Glu) rs756764400 0.00001
NM_004408.4(DNM1):c.1423-8C>A rs555786484 0.00001
NM_004408.4(DNM1):c.1558-3C>T rs546517702 0.00001
NM_004408.4(DNM1):c.1889T>C (p.Val630Ala) rs1295777740 0.00001
NM_004408.4(DNM1):c.1906-6T>C rs138961089 0.00001
NM_004408.4(DNM1):c.2561G>A (p.Arg854His) rs781345149 0.00001
NM_004408.4(DNM1):c.748G>A (p.Ala250Thr) rs1422655933 0.00001
NM_004408.3:c.1423-?_1671+?del
NM_004408.4(DNM1):c.1047T>G (p.Asp349Glu) rs1247861339
NM_004408.4(DNM1):c.1123G>A (p.Val375Ile) rs2131174031
NM_004408.4(DNM1):c.1128+4G>A rs768339660
NM_004408.4(DNM1):c.1129-9del rs2131174977
NM_004408.4(DNM1):c.1336-7T>A rs550764968
NM_004408.4(DNM1):c.1375A>G (p.Ile459Val) rs2131227049
NM_004408.4(DNM1):c.1427T>C (p.Met476Thr) rs2131251361
NM_004408.4(DNM1):c.1493+14del rs371426966
NM_004408.4(DNM1):c.2076+23del rs1237872802
NM_004408.4(DNM1):c.2156C>G (p.Ala719Gly) rs1432815882
NM_004408.4(DNM1):c.2582C>G (p.Pro861Arg) rs187315526
NM_004408.4(DNM1):c.825C>G (p.Pro275=) rs1588357060
NM_004408.4(DNM1):c.992+13C>T

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