ClinVar Miner

List of variants in gene OTOG reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
Download table as spreadsheet
HGVS dbSNP
NM_001277269.1(OTOG):c.1032+9C>A rs147843540
NM_001277269.1(OTOG):c.1095C>T (p.Val365=) rs74921579
NM_001277269.1(OTOG):c.1140-4A>C rs149163390
NM_001277269.1(OTOG):c.1251T>C (p.Thr417=) rs73418062
NM_001277269.1(OTOG):c.1376A>G (p.Asn459Ser) rs115772736
NM_001277269.1(OTOG):c.1833G>A (p.Arg611=) rs73418068
NM_001277269.1(OTOG):c.2134G>A (p.Ala712Thr) rs113745835
NM_001277269.1(OTOG):c.21G>A (p.Ala7=) rs149500671
NM_001277269.1(OTOG):c.2775G>A (p.Ser925=) rs55881341
NM_001277269.1(OTOG):c.2808C>T (p.His936=) rs61910692
NM_001277269.1(OTOG):c.3132C>T (p.Asn1044=) rs75133799
NM_001277269.1(OTOG):c.3325-8C>G rs12792504
NM_001277269.1(OTOG):c.3335C>T (p.Ala1112Val) rs7936324
NM_001277269.1(OTOG):c.3386C>T (p.Pro1129Leu) rs7936354
NM_001277269.1(OTOG):c.3387G>A (p.Pro1129=) rs146781877
NM_001277269.1(OTOG):c.3459C>T (p.Leu1153=) rs7122875
NM_001277269.1(OTOG):c.3561+10C>A rs113275496
NM_001277269.1(OTOG):c.3654C>T (p.Ser1218=) rs143393149
NM_001277269.1(OTOG):c.3710G>A (p.Arg1237His) rs116947228
NM_001277269.1(OTOG):c.421+7C>T rs139222878
NM_001277269.1(OTOG):c.4274G>A (p.Arg1425Gln) rs143848095
NM_001277269.1(OTOG):c.4663G>A (p.Ala1555Thr) rs545740473
NM_001277269.1(OTOG):c.5271C>A (p.Leu1757=) rs193083374
NM_001277269.1(OTOG):c.5495C>G (p.Ala1832Gly) rs1003490
NM_001277269.1(OTOG):c.570C>T (p.Ser190=) rs61995706
NM_001277269.1(OTOG):c.5804T>C (p.Met1935Thr) rs61732913
NM_001277269.1(OTOG):c.5864C>T (p.Thr1955Met) rs75677194
NM_001277269.1(OTOG):c.6329-7C>T rs143985593
NM_001277269.1(OTOG):c.675G>T (p.Glu225Asp) rs61736015
NM_001277269.1(OTOG):c.6811G>A (p.Ala2271Thr) rs116503251
NM_001277269.1(OTOG):c.7045G>C (p.Val2349Leu) rs540794663
NM_001277269.1(OTOG):c.7081A>G (p.Ile2361Val) rs191722806
NM_001277269.1(OTOG):c.724G>A (p.Ala242Thr) rs61910753
NM_001277269.1(OTOG):c.7366G>A (p.Gly2456Ser) rs61745322
NM_001277269.1(OTOG):c.7571G>A (p.Arg2524His) rs114242958
NM_001277269.1(OTOG):c.7686C>T (p.Ile2562=) rs187445787
NM_001277269.1(OTOG):c.7861C>A (p.Gln2621Lys) rs61995750
NM_001277269.1(OTOG):c.8071C>T (p.Arg2691Cys) rs567966154
NM_001277269.1(OTOG):c.8204T>C (p.Leu2735Pro) rs180703235
NM_001277269.1(OTOG):c.8298C>T (p.Phe2766=) rs61730948
NM_001277269.1(OTOG):c.8578-8C>T rs182750732
NM_001277269.1(OTOG):c.8682G>A (p.Leu2894=) rs542151771
NM_001277269.1(OTOG):c.879G>A (p.Lys293=) rs570688276
NM_001277269.2(OTOG):c.2250C>T (p.Cys750=) rs529043916
NM_001277269.2(OTOG):c.5730A>G (p.Val1910=) rs573436885
NM_001277269.2(OTOG):c.5955G>A (p.Thr1985=) rs570611759
NM_001277269.2(OTOG):c.6048C>T (p.Asp2016=) rs61734252
NM_001277269.2(OTOG):c.[805G>A] rs61978648
NM_001277269.2(OTOG):c.[8405G>A] rs117315845
NM_001277269.2(OTOG):c.[8526G>C] rs61997203

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.