ClinVar Miner

List of variants in gene ORC1 reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004153.4(ORC1):c.568G>A (p.Val190Met) rs3087477 0.02312
NM_004153.4(ORC1):c.2447T>C (p.Met816Thr) rs34521609 0.01742
NM_004153.4(ORC1):c.1115C>T (p.Ala372Val) rs3087476 0.01375
NM_004153.4(ORC1):c.1406G>A (p.Cys469Tyr) rs3087483 0.01081
NM_004153.4(ORC1):c.1397C>T (p.Thr466Met) rs3087481 0.00702
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.1186C>T (p.Arg396Trp) rs114426997 0.00382
NM_004153.4(ORC1):c.2226C>A (p.Ser742=) rs34644009 0.00271
NM_004153.4(ORC1):c.2427G>A (p.Glu809=) rs77077945 0.00224
NM_004153.4(ORC1):c.403-7A>C rs199834691 0.00197
NM_004153.4(ORC1):c.1819A>G (p.Thr607Ala) rs139027440 0.00130
NM_004153.4(ORC1):c.1318T>C (p.Ser440Pro) rs61756136 0.00066
NM_004153.4(ORC1):c.1581A>G (p.Gly527=) rs141066689 0.00056
NM_004153.4(ORC1):c.1517G>A (p.Cys506Tyr) rs147904927 0.00021
NM_004153.4(ORC1):c.1239A>C (p.Ala413=) rs377164890 0.00019
NM_004153.4(ORC1):c.314G>A (p.Arg105Gln) rs143141689 0.00016
NM_004153.4(ORC1):c.2436G>A (p.Pro812=) rs776580786 0.00006
NM_004153.4(ORC1):c.943C>T (p.Arg315Cys) rs201265198 0.00006
NM_004153.4(ORC1):c.608C>T (p.Thr203Ile) rs202095223 0.00005
NM_004153.4(ORC1):c.400C>T (p.Arg134Trp) rs587780413 0.00004
NM_004153.4(ORC1):c.2571G>A (p.Ala857=) rs192392819 0.00003
NM_004153.4(ORC1):c.2159G>A (p.Arg720Gln) rs387906828 0.00002
NM_004153.4(ORC1):c.2347G>A (p.Ala783Thr) rs779410890 0.00001
NM_004153.4(ORC1):c.325G>A (p.Ala109Thr) rs780169538 0.00001
NM_004153.4(ORC1):c.387C>T (p.Ile129=) rs886046400 0.00001
NM_004153.4(ORC1):c.1083-4G>C rs797045850
NM_004153.4(ORC1):c.1295C>G (p.Pro432Arg) rs1467460972
NM_004153.4(ORC1):c.2405A>G (p.His802Arg) rs587780411
NM_004153.4(ORC1):c.2518G>A (p.Asp840Asn) rs587780412
NM_004153.4(ORC1):c.308T>C (p.Leu103Ser) rs587780410
NM_004153.4(ORC1):c.625G>A (p.Ala209Thr) rs1553148123
NM_004153.4(ORC1):c.703A>G (p.Lys235Glu) rs797045851

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.