ClinVar Miner

List of variants in gene OTOG studied for Deafness, autosomal recessive 18b

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Total variants: 17
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HGVS dbSNP
NM_001277269.1(OTOG):c.1220A>C (p.Gln407Pro) rs876657936
NM_001277269.1(OTOG):c.1876C>T (p.Arg626Trp) rs201183725
NM_001277269.1(OTOG):c.2500C>T (p.Gln834Ter) rs554847663
NM_001277269.1(OTOG):c.330C>G (p.Tyr110Ter) rs574007567
NM_001277269.1(OTOG):c.433G>A (p.Gly145Ser) rs186893662
NM_001277269.1(OTOG):c.4877C>T (p.Pro1626Leu) rs897939885
NM_001277269.1(OTOG):c.5381T>C (p.Leu1794Pro) rs61744602
NM_001277269.1(OTOG):c.5508del (p.Ala1838fs) rs1029389440
NM_001277269.1(OTOG):c.6215G>A (p.Arg2072His) rs188527711
NM_001277269.1(OTOG):c.6347C>T (p.Pro2116Leu) rs397514607
NM_001277269.1(OTOG):c.6559C>T (p.Arg2187Ter) rs397514608
NM_001277269.1(OTOG):c.7003C>T (p.Arg2335Trp) rs755149839
NM_001277269.1(OTOG):c.7453C>T (p.Arg2485Ter) rs866476223
NM_001277269.1(OTOG):c.7729+1G>A rs548496846
NM_001277269.1(OTOG):c.7896G>A (p.Trp2632Ter) rs1565129771
NM_001277269.1(OTOG):c.935A>G (p.His312Arg) rs189159426
NM_001277269.1(OTOG):c.952G>A (p.Ala318Thr) rs553079779

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