ClinVar Miner

List of variants in gene OTOF reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
Download table as spreadsheet
HGVS dbSNP
NM_194248.3(OTOF):c.1471C>T (p.Leu491Phe)
NM_194248.3(OTOF):c.152C>T (p.Pro51Leu) rs150132765
NM_194248.3(OTOF):c.1530C>T (p.Ile510=) rs150452778
NM_194248.3(OTOF):c.1630C>T (p.Arg544Cys) rs139954767
NM_194248.3(OTOF):c.1803+7dup rs755835793
NM_194248.3(OTOF):c.1912G>T (p.Gly638Cys) rs1131691297
NM_194248.3(OTOF):c.2123G>A (p.Arg708Gln) rs145019640
NM_194248.3(OTOF):c.2215-80T>C rs143141993
NM_194248.3(OTOF):c.224A>G (p.Asn75Ser) rs775875524
NM_194248.3(OTOF):c.2253G>A (p.Thr751=) rs201888333
NM_194248.3(OTOF):c.2359C>T (p.Arg787Cys) rs574277214
NM_194248.3(OTOF):c.2375G>A (p.Arg792Gln) rs144800506
NM_194248.3(OTOF):c.245G>A (p.Arg82His) rs149766574
NM_194248.3(OTOF):c.2567A>T (p.Asn856Ile) rs752804141
NM_194248.3(OTOF):c.2575C>T (p.Arg859Cys) rs199603169
NM_194248.3(OTOF):c.2690G>A (p.Arg897Gln) rs760896684
NM_194248.3(OTOF):c.2693G>A (p.Gly898Asp) rs772312557
NM_194248.3(OTOF):c.2848G>A (p.Val950Ile) rs199613764
NM_194248.3(OTOF):c.2882A>G (p.Gln961Arg) rs1358025747
NM_194248.3(OTOF):c.3203G>A (p.Arg1068His) rs180748688
NM_194248.3(OTOF):c.327+10C>A rs377042002
NM_194248.3(OTOF):c.3277G>A (p.Glu1093Lys) rs1064795233
NM_194248.3(OTOF):c.339C>T (p.Cys113=) rs139098225
NM_194248.3(OTOF):c.3571G>T (p.Asp1191Tyr) rs772807679
NM_194248.3(OTOF):c.3637G>A (p.Gly1213Ser) rs140023414
NM_194248.3(OTOF):c.3680G>A (p.Arg1227Gln) rs759559737
NM_194248.3(OTOF):c.3694C>T (p.Arg1232Trp) rs749458515
NM_194248.3(OTOF):c.3865-2A>G rs1131691278
NM_194248.3(OTOF):c.3939G>A (p.Ala1313=) rs149566576
NM_194248.3(OTOF):c.40C>T (p.Arg14Trp)
NM_194248.3(OTOF):c.4334A>G (p.Glu1445Gly) rs1131691695
NM_194248.3(OTOF):c.4463A>T (p.Asp1488Val) rs142284613
NM_194248.3(OTOF):c.446C>T (p.Thr149Met) rs140454738
NM_194248.3(OTOF):c.4483C>A (p.Arg1495=) rs147321712
NM_194248.3(OTOF):c.4548C>T (p.Tyr1516=) rs139525746
NM_194248.3(OTOF):c.4820G>A (p.Arg1607Gln) rs141800430
NM_194248.3(OTOF):c.4894C>A (p.Pro1632Thr)
NM_194248.3(OTOF):c.4922G>A (p.Arg1641His) rs200283244
NM_194248.3(OTOF):c.4946T>C (p.Ile1649Thr) rs146618661
NM_194248.3(OTOF):c.5083G>T (p.Asp1695Tyr) rs144422709
NM_194248.3(OTOF):c.5254T>C (p.Phe1752Leu) rs1085307832
NM_194248.3(OTOF):c.5292-9C>T rs372713647
NM_194248.3(OTOF):c.5332G>T (p.Val1778Phe) rs111033330
NM_194248.3(OTOF):c.5394C>T (p.Asp1798=) rs111033366
NM_194248.3(OTOF):c.5479C>T (p.Arg1827Trp) rs142748621
NM_194248.3(OTOF):c.5632G>A (p.Val1878Met) rs757360892
NM_194248.3(OTOF):c.5742G>A (p.Leu1914=) rs141235641
NM_194248.3(OTOF):c.578G>T (p.Arg193Ile) rs139779680
NM_194248.3(OTOF):c.5815C>T (p.Arg1939Trp) rs368790049
NM_194248.3(OTOF):c.5829C>T (p.Ser1943=)
NM_194248.3(OTOF):c.843C>T (p.Asp281=) rs368728682

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.