ClinVar Miner

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

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Total variants: 46
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HGVS dbSNP
NM_001277269.1(OTOG):c.1321C>T (p.Arg441Trp) rs199968574
NM_001277269.1(OTOG):c.1359C>T (p.Asp453=) rs571886426
NM_001277269.1(OTOG):c.1405G>A (p.Val469Met) rs756129872
NM_001277269.1(OTOG):c.1796T>C (p.Ile599Thr) rs751269089
NM_001277269.1(OTOG):c.1833G>A (p.Arg611=) rs73418068
NM_001277269.1(OTOG):c.2434G>A (p.Asp812Asn) rs141010212
NM_001277269.1(OTOG):c.2548G>C (p.Gly850Arg) rs61734214
NM_001277269.1(OTOG):c.2597+9C>T rs528157125
NM_001277269.1(OTOG):c.2759G>T (p.Arg920Leu) rs144060182
NM_001277269.1(OTOG):c.2919C>T (p.Gly973=) rs893483749
NM_001277269.1(OTOG):c.3003G>A (p.Pro1001=) rs11024331
NM_001277269.1(OTOG):c.3336G>A (p.Ala1112=) rs539192142
NM_001277269.1(OTOG):c.3561+37C>T rs117718159
NM_001277269.1(OTOG):c.371C>G (p.Ala124Gly) rs545257884
NM_001277269.1(OTOG):c.4274G>A (p.Arg1425Gln) rs143848095
NM_001277269.1(OTOG):c.4857G>A (p.Ser1619=) rs369768224
NM_001277269.1(OTOG):c.4902C>T (p.Val1634=) rs780581249
NM_001277269.1(OTOG):c.5381T>C (p.Leu1794Pro) rs61744602
NM_001277269.1(OTOG):c.6160-73G>T rs77217986
NM_001277269.1(OTOG):c.627T>G (p.Ala209=) rs562856597
NM_001277269.1(OTOG):c.6929G>A (p.Arg2310His) rs142799217
NM_001277269.1(OTOG):c.7389A>C (p.Gln2463His) rs145833172
NM_001277269.1(OTOG):c.7902C>T (p.Pro2634=) rs200566292
NM_001277269.1(OTOG):c.8040C>T (p.Tyr2680=) rs892246727
NM_001277269.1(OTOG):c.8058G>A (p.Pro2686=) rs753850661
NM_001277269.1(OTOG):c.8071C>T (p.Arg2691Cys) rs567966154
NM_001277269.1(OTOG):c.8498-55T>C rs76783895
NM_001277269.1(OTOG):c.8682G>A (p.Leu2894=) rs542151771
NM_001277269.1(OTOG):c.879G>A (p.Lys293=) rs570688276
NM_001277269.1(OTOG):c.915C>T (p.Asp305=) rs144220847
NM_001277269.2(OTOG):c.4298G>A (p.Arg1433Gln) rs778218478
NM_001277269.2(OTOG):c.8574C>T (p.Thr2858=) rs201952556
NM_001277269.2(OTOG):c.[3719C>T] rs117005078
NM_001277269.2(OTOG):c.[4058G>A] rs145689709
NM_001277269.2(OTOG):c.[6110C>T] rs61736002
NM_001277269.2(OTOG):c.[8405G>A] rs117315845
NM_001292063.2(OTOG):c.1560C>T (p.Phe520=) rs1482605363
NM_001292063.2(OTOG):c.441C>T (p.His147=) rs567294014
NM_001292063.2(OTOG):c.5121T>G (p.Val1707=) rs563661860
NM_001292063.2(OTOG):c.5549C>G (p.Pro1850Arg) rs376684690
NM_001292063.2(OTOG):c.7557G>A (p.Glu2519=) rs577246890
NM_001292063.2(OTOG):c.7800T>C (p.Cys2600=) rs1333602999
NM_001292063.2(OTOG):c.7827G>A (p.Gln2609=) rs1351651117
NM_001292063.2(OTOG):c.7962G>A (p.Glu2654=) rs976702124
NM_001292063.2(OTOG):c.8190+8G>A rs1258304711
NM_001292063.2(OTOG):c.8718C>G (p.Thr2906=) rs1195829508

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