ClinVar Miner

List of variants in gene OTOF reported as uncertain significance for Nonsyndromic Hearing Loss, Recessive

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Total variants: 72
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HGVS dbSNP
NM_194248.3(OTOF):c.*105C>T rs145899319
NM_194248.3(OTOF):c.*126G>A rs73920281
NM_194248.3(OTOF):c.*341G>A rs549185736
NM_194248.3(OTOF):c.*440T>C rs112949167
NM_194248.3(OTOF):c.*770T>A rs886055872
NM_194248.3(OTOF):c.*867C>T rs578132477
NM_194248.3(OTOF):c.*898C>A rs886055871
NM_194248.3(OTOF):c.-110_-108AGG[3] rs886055882
NM_194248.3(OTOF):c.-113G>A rs79734645
NM_194248.3(OTOF):c.-120G>T rs114469860
NM_194248.3(OTOF):c.-43T>A rs201812205
NM_194248.3(OTOF):c.-54G>A rs571817012
NM_194248.3(OTOF):c.-64G>A rs886055881
NM_194248.3(OTOF):c.-67G>A rs13422586
NM_194248.3(OTOF):c.-73G>A rs550236431
NM_194248.3(OTOF):c.-91G>A rs139010880
NM_194248.3(OTOF):c.1035C>T (p.Tyr345=) rs138885901
NM_194248.3(OTOF):c.1045+4A>G rs754376415
NM_194248.3(OTOF):c.1149G>C (p.Gly383=) rs142219516
NM_194248.3(OTOF):c.1206-10G>A rs769631334
NM_194248.3(OTOF):c.1227G>C (p.Gly409=) rs886055879
NM_194248.3(OTOF):c.1424A>G (p.Glu475Gly) rs111033396
NM_194248.3(OTOF):c.1570G>A (p.Gly524Arg) rs146739635
NM_194248.3(OTOF):c.1630C>T (p.Arg544Cys) rs139954767
NM_194248.3(OTOF):c.1640C>T (p.Thr547Met) rs200191563
NM_194248.3(OTOF):c.1803+13G>A rs886055878
NM_194248.3(OTOF):c.1961G>A (p.Arg654Gln) rs184605839
NM_194248.3(OTOF):c.1977G>A (p.Pro659=) rs145589784
NM_194248.3(OTOF):c.2106T>A (p.His702Gln) rs764458682
NM_194248.3(OTOF):c.2374C>T (p.Arg792Trp) rs148532589
NM_194248.3(OTOF):c.245G>A (p.Arg82His) rs149766574
NM_194248.3(OTOF):c.2498A>T (p.Gln833Leu) rs191568463
NM_194248.3(OTOF):c.2523+5G>A rs201745796
NM_194248.3(OTOF):c.2575C>T (p.Arg859Cys) rs199603169
NM_194248.3(OTOF):c.2605G>T (p.Asp869Tyr) rs886055877
NM_194248.3(OTOF):c.2702C>T (p.Ser901Leu) rs200599474
NM_194248.3(OTOF):c.2788C>G (p.Pro930Ala) rs746541787
NM_194248.3(OTOF):c.2807T>A (p.Val936Asp) rs758010380
NM_194248.3(OTOF):c.2859C>T (p.Val953=) rs77414333
NM_194248.3(OTOF):c.297G>A (p.Thr99=) rs397517941
NM_194248.3(OTOF):c.2992-14A>G rs370041999
NM_194248.3(OTOF):c.3189G>A (p.Ala1063=) rs80356573
NM_194248.3(OTOF):c.3230A>G (p.Gln1077Arg) rs749183807
NM_194248.3(OTOF):c.327+5G>T rs370643920
NM_194248.3(OTOF):c.3599C>T (p.Pro1200Leu) rs762316974
NM_194248.3(OTOF):c.3608A>G (p.Asn1203Ser) rs61740776
NM_194248.3(OTOF):c.366C>T (p.Asp122=) rs61747283
NM_194248.3(OTOF):c.3749G>A (p.Arg1250His) rs755411269
NM_194248.3(OTOF):c.3918G>C (p.Lys1306Asn) rs774929350
NM_194248.3(OTOF):c.4092C>G (p.Gly1364=) rs779854387
NM_194248.3(OTOF):c.4239A>G (p.Lys1413=) rs886055876
NM_194248.3(OTOF):c.4290C>T (p.Asn1430=) rs566846495
NM_194248.3(OTOF):c.447G>A (p.Thr149=) rs151257291
NM_194248.3(OTOF):c.4629-9C>T rs72853726
NM_194248.3(OTOF):c.4800-11C>T rs41286009
NM_194248.3(OTOF):c.505C>T (p.Arg169Trp) rs61744348
NM_194248.3(OTOF):c.506G>A (p.Arg169Gln) rs149701372
NM_194248.3(OTOF):c.509+11G>A rs200010052
NM_194248.3(OTOF):c.5097C>G (p.Ile1699Met) rs12386239
NM_194248.3(OTOF):c.5193-9T>C rs886055875
NM_194248.3(OTOF):c.51C>T (p.Gly17=) rs142333075
NM_194248.3(OTOF):c.5440A>G (p.Met1814Val) rs886055874
NM_194248.3(OTOF):c.5460C>T (p.Thr1820=) rs148749290
NM_194248.3(OTOF):c.5477C>T (p.Ala1826Val) rs377197565
NM_194248.3(OTOF):c.5623G>A (p.Val1875Met) rs370691004
NM_194248.3(OTOF):c.5650A>G (p.Lys1884Glu) rs886055873
NM_194248.3(OTOF):c.5742G>A (p.Leu1914=) rs141235641
NM_194248.3(OTOF):c.576A>G (p.Gln192=) rs886055880
NM_194248.3(OTOF):c.591G>A (p.Pro197=) rs779916426
NM_194248.3(OTOF):c.611A>C (p.Asp204Ala) rs756388245
NM_194248.3(OTOF):c.960G>A (p.Ser320=) rs141463872
NM_194248.3(OTOF):c.97C>T (p.Arg33Trp) rs150867836

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