ClinVar Miner

List of variants in gene OTOF reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NC_000002.12:g.26461946G>A
NM_194248.3(OTOF):c.-113G>A rs79734645
NM_194248.3(OTOF):c.-43T>A rs201812205
NM_194248.3(OTOF):c.1424A>G (p.Glu475Gly) rs111033396
NM_194248.3(OTOF):c.2215-80T>C rs143141993
NM_194248.3(OTOF):c.234C>T (p.Ile78=)
NM_194248.3(OTOF):c.2375G>A (p.Arg792Gln) rs144800506
NM_194248.3(OTOF):c.2580C>A (p.Val860=)
NM_194248.3(OTOF):c.2580C>T (p.Val860=)
NM_194248.3(OTOF):c.3384C>T (p.Pro1128=) rs145151677
NM_194248.3(OTOF):c.367G>A (p.Gly123Ser) rs116314622
NM_194248.3(OTOF):c.3733+39C>T
NM_194248.3(OTOF):c.3734-10A>C rs73920284
NM_194248.3(OTOF):c.3966C>G (p.Asp1322Glu) rs80356576
NM_194248.3(OTOF):c.42G>A (p.Arg14=) rs6734111
NM_194248.3(OTOF):c.4582G>A (p.Asp1528Asn) rs138151478
NM_194248.3(OTOF):c.5039G>A (p.Arg1680His) rs11893228
NM_194248.3(OTOF):c.5160G>A (p.Thr1720=)
NM_194248.3(OTOF):c.5694C>T (p.Asn1898=)
NM_194248.3(OTOF):c.578G>T (p.Arg193Ile) rs139779680
NM_194248.3(OTOF):c.633G>C (p.Arg211=)

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