ClinVar Miner

List of variants in gene OTOA reported as likely benign for not specified

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Gene type:
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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_144672.4(OTOA):c.2417A>C (p.Tyr806Ser) rs464691 0.00141
NM_144672.4(OTOA):c.236G>A (p.Arg79Gln) rs147088274 0.00067
NM_144672.4(OTOA):c.120+10C>G rs200215069 0.00046
NM_144672.4(OTOA):c.2207+9C>T rs374535775 0.00038
NM_144672.4(OTOA):c.1320+19C>T rs199792638 0.00026
NM_144672.4(OTOA):c.739+11A>G rs186092865 0.00026
NM_144672.4(OTOA):c.2019C>T (p.Asp673=) rs147901051 0.00022
NM_144672.4(OTOA):c.660C>T (p.Tyr220=) rs139292090 0.00020
NM_144672.4(OTOA):c.1521C>T (p.Ile507=) rs140579035 0.00019
NM_144672.4(OTOA):c.1821G>A (p.Ala607=) rs143993346 0.00015
NM_144672.4(OTOA):c.1806+4C>A rs201545393 0.00014
NM_144672.4(OTOA):c.396C>T (p.Gly132=) rs147717988 0.00010
NM_144672.4(OTOA):c.180-12C>T rs776210902 0.00009
NM_144672.4(OTOA):c.2153A>G (p.Asp718Gly) rs767518359 0.00009
NM_144672.4(OTOA):c.2133C>T (p.His711=) rs201907941 0.00004
NM_144672.4(OTOA):c.645G>A (p.Val215=) rs759683702 0.00004
NM_144672.4(OTOA):c.1353C>T (p.Gly451=) rs374219815 0.00003
NM_144672.4(OTOA):c.981-125T>C rs201435154 0.00003
NM_144672.4(OTOA):c.1141C>G (p.Gln381Glu) rs377581131 0.00002
NM_144672.4(OTOA):c.987G>A (p.Gly329=) rs758229970 0.00002
NM_144672.4(OTOA):c.1104+12G>C rs143853515
NM_144672.4(OTOA):c.1105-10C>T rs727503349
NM_144672.4(OTOA):c.1500G>C (p.Ala500=) rs199908646

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