ClinVar Miner

List of variants in gene ORC1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 131
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HGVS dbSNP gnomAD frequency
NM_004153.4(ORC1):c.1115C>T (p.Ala372Val) rs3087476 0.01375
NM_004153.4(ORC1):c.806C>T (p.Ser269Leu) rs61753390 0.00653
NM_004153.4(ORC1):c.2314G>A (p.Val772Ile) rs61753389 0.00503
NM_004153.4(ORC1):c.57G>C (p.Arg19Ser) rs3087473 0.00472
NM_004153.4(ORC1):c.2226C>A (p.Ser742=) rs34644009 0.00271
NM_004153.4(ORC1):c.1671C>T (p.Ala557=) rs61756137 0.00097
NM_004153.4(ORC1):c.2162G>A (p.Arg721Gln) rs142127656 0.00084
NM_004153.4(ORC1):c.2580C>T (p.Asp860=) rs61756139 0.00065
NM_004153.4(ORC1):c.1581A>G (p.Gly527=) rs141066689 0.00056
NM_004153.4(ORC1):c.1405T>C (p.Cys469Arg) rs144848215 0.00043
NM_004153.4(ORC1):c.1092A>G (p.Lys364=) rs61756134 0.00034
NM_004153.4(ORC1):c.1239A>C (p.Ala413=) rs377164890 0.00019
NM_004153.4(ORC1):c.2382G>A (p.Thr794=) rs146844078 0.00016
NM_004153.4(ORC1):c.1365G>A (p.Thr455=) rs372781874 0.00014
NM_004153.4(ORC1):c.1482-18G>A rs367740707 0.00010
NM_004153.4(ORC1):c.2463C>T (p.Ala821=) rs139714078 0.00010
NM_004153.4(ORC1):c.1161T>G (p.Thr387=) rs554803101 0.00009
NM_004153.4(ORC1):c.223+16G>A rs754879040 0.00006
NM_004153.4(ORC1):c.2346C>T (p.Leu782=) rs142257783 0.00006
NM_004153.4(ORC1):c.2436G>A (p.Pro812=) rs776580786 0.00006
NM_004153.4(ORC1):c.1722G>A (p.Thr574=) rs141804338 0.00005
NM_004153.4(ORC1):c.1440T>C (p.Ala480=) rs543395954 0.00004
NM_004153.4(ORC1):c.151C>G (p.Gln51Glu) rs182707743 0.00004
NM_004153.4(ORC1):c.1668A>G (p.Gln556=) rs367868420 0.00004
NM_004153.4(ORC1):c.1941T>C (p.Leu647=) rs200575804 0.00004
NM_004153.4(ORC1):c.2294C>T (p.Thr765Met) rs760741211 0.00004
NM_004153.4(ORC1):c.42T>C (p.Tyr14=) rs1431067797 0.00004
NM_004153.4(ORC1):c.999G>A (p.Glu333=) rs373454397 0.00004
NM_004153.4(ORC1):c.2304-13C>T rs761928972 0.00003
NM_004153.4(ORC1):c.2571G>A (p.Ala857=) rs192392819 0.00003
NM_004153.4(ORC1):c.1575T>C (p.His525=) rs770310076 0.00002
NM_004153.4(ORC1):c.1707T>C (p.Asn569=) rs376619175 0.00002
NM_004153.4(ORC1):c.807G>A (p.Ser269=) rs769149749 0.00002
NM_004153.4(ORC1):c.933A>G (p.Ser311=) rs760334954 0.00002
NM_004153.4(ORC1):c.1864-8C>T rs367621377 0.00001
NM_004153.4(ORC1):c.1866C>T (p.Leu622=) rs201622141 0.00001
NM_004153.4(ORC1):c.223+8T>G rs752809695 0.00001
NM_004153.4(ORC1):c.2286A>G (p.Ser762=) rs745934726 0.00001
NM_004153.4(ORC1):c.2295G>T (p.Thr765=) rs566116666 0.00001
NM_004153.4(ORC1):c.2343C>T (p.Ile781=) rs201137221 0.00001
NM_004153.4(ORC1):c.2568T>C (p.Tyr856=) rs1476680511 0.00001
NM_004153.4(ORC1):c.61T>C (p.Leu21=) rs1207944564 0.00001
NM_004153.4(ORC1):c.669A>G (p.Gln223=) rs775173361 0.00001
NM_004153.4(ORC1):c.990T>C (p.Ile330=) rs747956708 0.00001
NM_004153.4(ORC1):c.1000A>C (p.Arg334=)
NM_004153.4(ORC1):c.1005A>G (p.Thr335=)
NM_004153.4(ORC1):c.1050C>G (p.Ser350=) rs370633393
NM_004153.4(ORC1):c.1187+11T>A
NM_004153.4(ORC1):c.1187+13C>T
NM_004153.4(ORC1):c.1187+15T>C
NM_004153.4(ORC1):c.1188-13C>T
NM_004153.4(ORC1):c.120T>A (p.Gly40=)
NM_004153.4(ORC1):c.1266C>T (p.Asp422=)
NM_004153.4(ORC1):c.126C>T (p.Ser42=)
NM_004153.4(ORC1):c.1278T>G (p.Ala426=)
NM_004153.4(ORC1):c.129C>T (p.Thr43=)
NM_004153.4(ORC1):c.1339T>C (p.Leu447=)
NM_004153.4(ORC1):c.1377G>A (p.Lys459=)
NM_004153.4(ORC1):c.1380G>A (p.Lys460=)
NM_004153.4(ORC1):c.1383+19del
NM_004153.4(ORC1):c.1383+20A>T
NM_004153.4(ORC1):c.1383+7T>C
NM_004153.4(ORC1):c.1384-17C>G
NM_004153.4(ORC1):c.1386C>T (p.Leu462=)
NM_004153.4(ORC1):c.1398G>T (p.Thr466=)
NM_004153.4(ORC1):c.1461G>T (p.Val487=)
NM_004153.4(ORC1):c.147T>C (p.Ile49=) rs1647702332
NM_004153.4(ORC1):c.1482-18G>T
NM_004153.4(ORC1):c.1482-4G>T
NM_004153.4(ORC1):c.1503T>C (p.Pro501=)
NM_004153.4(ORC1):c.1540A>G (p.Ile514Val)
NM_004153.4(ORC1):c.1578C>T (p.Thr526=)
NM_004153.4(ORC1):c.1583+12G>A rs1472649440
NM_004153.4(ORC1):c.1584-11T>C
NM_004153.4(ORC1):c.1584-12C>T
NM_004153.4(ORC1):c.1584-20G>A
NM_004153.4(ORC1):c.1587C>T (p.Cys529=)
NM_004153.4(ORC1):c.1599C>T (p.Ser533=)
NM_004153.4(ORC1):c.1764A>G (p.Thr588=)
NM_004153.4(ORC1):c.1812A>G (p.Gln604=)
NM_004153.4(ORC1):c.1863+10C>T
NM_004153.4(ORC1):c.1863+13T>G
NM_004153.4(ORC1):c.1863+14G>C
NM_004153.4(ORC1):c.1863+16G>A
NM_004153.4(ORC1):c.1863+18G>A
NM_004153.4(ORC1):c.1864-12T>C
NM_004153.4(ORC1):c.1864-5G>T
NM_004153.4(ORC1):c.1932G>A (p.Glu644=)
NM_004153.4(ORC1):c.19A>C (p.Arg7=)
NM_004153.4(ORC1):c.2013+19C>T
NM_004153.4(ORC1):c.2014-8C>T
NM_004153.4(ORC1):c.2043T>C (p.Tyr681=)
NM_004153.4(ORC1):c.2127C>T (p.Ala709=)
NM_004153.4(ORC1):c.2160A>G (p.Arg720=)
NM_004153.4(ORC1):c.223+10G>A
NM_004153.4(ORC1):c.224-14C>T
NM_004153.4(ORC1):c.224-17C>T rs2147943062
NM_004153.4(ORC1):c.224-19T>C
NM_004153.4(ORC1):c.2265G>C (p.Val755=) rs1569900704
NM_004153.4(ORC1):c.2303+10T>C rs748117291
NM_004153.4(ORC1):c.2304-8C>A
NM_004153.4(ORC1):c.2391+6CTC[2]
NM_004153.4(ORC1):c.2511C>T (p.Ser837=) rs1216718483
NM_004153.4(ORC1):c.2517C>T (p.Asn839=)
NM_004153.4(ORC1):c.2544C>T (p.Asn848=)
NM_004153.4(ORC1):c.2553G>A (p.Gln851=)
NM_004153.4(ORC1):c.307T>C (p.Leu103=) rs372824271
NM_004153.4(ORC1):c.33A>G (p.Arg11=)
NM_004153.4(ORC1):c.378G>A (p.Ala126=)
NM_004153.4(ORC1):c.402+15C>T
NM_004153.4(ORC1):c.402+19C>T
NM_004153.4(ORC1):c.501A>G (p.Pro167=)
NM_004153.4(ORC1):c.522G>A (p.Ala174=)
NM_004153.4(ORC1):c.522G>C (p.Ala174=)
NM_004153.4(ORC1):c.540A>G (p.Gln180=)
NM_004153.4(ORC1):c.567C>T (p.Pro189=)
NM_004153.4(ORC1):c.591A>G (p.Ala197=)
NM_004153.4(ORC1):c.603T>C (p.Ser201=)
NM_004153.4(ORC1):c.615A>G (p.Ala205=)
NM_004153.4(ORC1):c.651C>T (p.Ser217=)
NM_004153.4(ORC1):c.699C>A (p.Ala233=) rs2147940713
NM_004153.4(ORC1):c.717T>C (p.Leu239=) rs1647377054
NM_004153.4(ORC1):c.721+16G>T
NM_004153.4(ORC1):c.722-17G>A
NM_004153.4(ORC1):c.744C>A (p.Ser248=) rs2147938061
NM_004153.4(ORC1):c.784A>G (p.Ile262Val)
NM_004153.4(ORC1):c.84C>T (p.Tyr28=)
NM_004153.4(ORC1):c.96-14C>T
NM_004153.4(ORC1):c.960C>G (p.Thr320=)
NM_004153.4(ORC1):c.975G>A (p.Ser325=)
NM_004153.4(ORC1):c.991A>C (p.Arg331=)

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