List of variants in gene OTOA reported as uncertain significance for not specified

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_144672.4(OTOA):c.2359G>T (p.Glu787Ter)	rs200988634	0.00927
NM_144672.4(OTOA):c.2353A>C (p.Thr785Pro)	rs464696	0.00839
NM_144672.4(OTOA):c.605G>C (p.Arg202Pro)	rs142850013	0.00029
NM_144672.4(OTOA):c.3377T>C (p.Leu1126Pro)	rs568139514	0.00014
NM_144672.4(OTOA):c.446C>A (p.Ala149Asp)	rs113820086	0.00008
NM_144672.4(OTOA):c.131T>C (p.Ile44Thr)	rs730882117	0.00006
NM_144672.4(OTOA):c.1807G>T (p.Val603Phe)	rs775686301	0.00004
NM_144672.4(OTOA):c.661G>A (p.Asp221Asn)	rs142693996	0.00003
NM_144672.4(OTOA):c.1907C>G (p.Ala636Gly)	rs780071647	0.00002
NM_144672.4(OTOA):c.775T>C (p.Trp259Arg)	rs1476325639	0.00002
NM_144672.4(OTOA):c.1292T>C (p.Leu431Ser)	rs1332276288	0.00001
NM_144672.4(OTOA):c.2305C>T (p.Pro769Ser)	rs769182891	0.00001
NM_144672.4(OTOA):c.401A>G (p.Asp134Gly)	rs753359371	0.00001
NM_144672.4(OTOA):c.1024G>C (p.Asp342His)	rs1597824772
NM_144672.4(OTOA):c.1109A>G (p.Lys370Arg)	rs727505354
NM_144672.4(OTOA):c.1172C>T (p.Ser391Leu)	rs727504599
NM_144672.4(OTOA):c.1186G>A (p.Gly396Ser)	rs1898305690
NM_144672.4(OTOA):c.1322T>C (p.Val441Ala)	rs1555499893
NM_144672.4(OTOA):c.1880C>G (p.Pro627Arg)	rs727503351
NM_144672.4(OTOA):c.2222G>C (p.Trp741Ser)	rs727505120
NM_144672.4(OTOA):c.851T>C (p.Phe284Ser)	rs727503348
NM_144672.4(OTOA):c.96G>T (p.Leu32Phe)	rs372826296

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