List of variants in gene OTOGL reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
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: 38

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001378609.3(OTOGL):c.3488A>G (p.Asp1163Gly)	rs202085918	0.00195
NM_001378609.3(OTOGL):c.6968G>A (p.Arg2323Gln)	rs143495342	0.00168
NM_001378609.3(OTOGL):c.1957T>G (p.Cys653Gly)	rs200364230	0.00159
NM_001378609.3(OTOGL):c.4906G>A (p.Glu1636Lys)	rs143817729	0.00134
NM_001378609.3(OTOGL):c.2456C>T (p.Ser819Leu)	rs199855270	0.00126
NM_001378609.3(OTOGL):c.860C>T (p.Ser287Leu)	rs147195954	0.00116
NM_001378609.3(OTOGL):c.2564C>T (p.Pro855Leu)	rs183159689	0.00111
NM_001378609.3(OTOGL):c.6229T>G (p.Cys2077Gly)	rs145929269	0.00110
NM_001378609.3(OTOGL):c.1815G>T (p.Gln605His)	rs192234924	0.00101
NM_001378609.3(OTOGL):c.4280-5T>C	rs200889330	0.00091
NM_001378609.3(OTOGL):c.2357T>C (p.Phe786Ser)	rs192944055	0.00088
NM_001378609.3(OTOGL):c.3020T>C (p.Val1007Ala)	rs202051419	0.00080
NM_001378609.3(OTOGL):c.3675G>C (p.Gln1225His)	rs139375212	0.00079
NM_001378609.3(OTOGL):c.2551G>A (p.Asp851Asn)	rs112430701	0.00072
NM_001378609.3(OTOGL):c.119+7A>G	rs753923439	0.00049
NM_001378609.3(OTOGL):c.4146C>A (p.Pro1382=)	rs374853700	0.00045
NM_001378609.3(OTOGL):c.792A>G (p.Gln264=)	rs144176460	0.00043
NM_001378609.3(OTOGL):c.2628C>T (p.Asn876=)	rs371565107	0.00030
NM_001378609.3(OTOGL):c.5736T>C (p.Val1912=)	rs368807465	0.00027
NM_001378609.3(OTOGL):c.2345C>T (p.Pro782Leu)	rs200797401	0.00024
NM_001378609.3(OTOGL):c.3393T>C (p.Tyr1131=)	rs574974638	0.00019
NM_001378609.3(OTOGL):c.3555C>T (p.Tyr1185=)	rs374198258	0.00016
NM_001378609.3(OTOGL):c.5502C>T (p.Ser1834=)	rs372006140	0.00015
NM_001378609.3(OTOGL):c.1111C>T (p.His371Tyr)	rs78377084	0.00014
NM_001378609.3(OTOGL):c.6882C>T (p.Asp2294=)	rs751285103	0.00010
NM_001378609.3(OTOGL):c.4446T>C (p.Tyr1482=)	rs376273459	0.00009
NM_001378609.3(OTOGL):c.5702T>C (p.Ile1901Thr)	rs775475186	0.00009
NM_001378609.3(OTOGL):c.3184A>T (p.Ile1062Phe)	rs188793584	0.00005
NM_001378609.3(OTOGL):c.2271C>T (p.Phe757=)	rs949936521	0.00001
NM_001378609.3(OTOGL):c.3450+9A>G	rs576035717	0.00001
NM_001378609.3(OTOGL):c.3804A>G (p.Ser1268=)	rs183046919	0.00001
NM_001378609.3(OTOGL):c.4764G>A (p.Lys1588=)	rs774916755	0.00001
NM_001378609.3(OTOGL):c.5095G>A (p.Gly1699Ser)	rs563989349	0.00001
NM_001378609.3(OTOGL):c.6226+14A>G	rs780160987	0.00001
NM_001378609.3(OTOGL):c.1077C>T (p.Cys359=)	rs876657559
NM_001378609.3(OTOGL):c.2391-12T>C	rs876657560
NM_001378609.3(OTOGL):c.4312A>G (p.Met1438Val)	rs1555298321
NM_001378609.3(OTOGL):c.4846C>A (p.Arg1616=)	rs536538111

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.