List of variants in gene OTOF reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_194248.3(OTOF):c.2215-19C>G	rs111033427	0.00434
NM_194248.3(OTOF):c.2215-77T>G	rs76130130	0.00341
NM_194248.3(OTOF):c.2215-80T>C	rs143141993	0.00268
NM_194248.3(OTOF):c.245G>A (p.Arg82His)	rs149766574	0.00237
NM_194248.3(OTOF):c.5742G>A (p.Leu1914=)	rs141235641	0.00191
NM_194248.3(OTOF):c.367G>A (p.Gly123Ser)	rs116314622	0.00134
NM_194248.3(OTOF):c.1530C>T (p.Ile510=)	rs150452778	0.00093
NM_194248.3(OTOF):c.237G>A (p.Gly79=)	rs117985483	0.00052
NM_194248.3(OTOF):c.5331C>T (p.Asp1777=)	rs141082575	0.00016
NM_194248.3(OTOF):c.5202G>A (p.Leu1734=)	rs770579181	0.00002
NM_194248.3(OTOF):c.2064T>C (p.Thr688=)
NM_194248.3(OTOF):c.2604G>A (p.Lys868=)
NM_194248.3(OTOF):c.51C>T (p.Gly17=)	rs142333075
NM_194248.3(OTOF):c.5487C>T (p.Thr1829=)
NM_194323.3(OTOF):c.3531C>T (p.Phe1177=)

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.