"GeneDx"[submitter] AND "OTOG"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1222674	NC_000011.10:g.17547064A>G	OTOG	Single nucleotide variant	not provided	GBenign
Select item 1197895	NM_001292063.2(OTOG):c.1A>G (p.Met1Val)	OTOG (M1V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1300734	NM_001292063.2(OTOG):c.13G>A (p.Ala5Thr)	OTOG (A5T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1803459	NM_001292063.2(OTOG):c.15G>A (p.Ala5=)	OTOG	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 504776	NM_001292063.2(OTOG):c.21G>A (p.Ala7=)	OTOG	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 515578	NM_001292063.2(OTOG):c.76C>T (p.Leu26=)	OTOG	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1208266	NM_001292063.2(OTOG):c.93C>T (p.Leu31=)	OTOG	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 1338903	NM_001292063.2(OTOG):c.94+17C>T	OTOG	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 1699851	NM_001292063.2(OTOG):c.94+36C>G	OTOG (R44G)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 226863	NM_001292063.2(OTOG):c.94+37G>A	OTOG (R44Q)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 1710601	NM_001292063.2(OTOG):c.94+62G>A	OTOG (M52I)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1906860	NM_001292063.2(OTOG):c.94+75G>A	OTOG (A57T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 506139	NM_001292063.2(OTOG):c.94+75G>T	OTOG (A57S)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 930090	NM_001292063.2(OTOG):c.94+76C>T	OTOG (A57V)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 1233627	NM_001292063.2(OTOG):c.95-82C>G	OTOG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 805106	NM_001292063.2(OTOG):c.106G>A (p.Val36Ile)	OTOG (V36I)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 805107	NM_001292063.2(OTOG):c.144C>G (p.Ala48=)	OTOG	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1181149	NM_001292063.2(OTOG):c.148C>G (p.Gln50Glu)	OTOG (Q50E)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 3253157	NM_001292063.2(OTOG):c.156-14C>T	OTOG (R60C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3378165	NM_001292063.2(OTOG):c.168G>C (p.Gln56His)	OTOG (Q56H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1215900	NM_001292063.2(OTOG):c.173C>T (p.Ala58Val)	OTOG (A58V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1262081	NM_001292063.2(OTOG):c.216+126A>G	OTOG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1216587	NM_001292063.2(OTOG):c.216+231_216+244del	OTOG	Deletion (intron variant)	not provided	GLikely benign
Select item 1213434	NM_001292063.2(OTOG):c.216+229_216+244del	OTOG	Deletion (intron variant)	not provided	GLikely benign
Select item 1211220	NM_001292063.2(OTOG):c.216+226_216+244del	OTOG	Deletion (intron variant)	not provided	GLikely benign
Select item 1203281	NM_001292063.2(OTOG):c.216+234_216+244del	OTOG	Deletion (intron variant)	not provided	GLikely benign
Select item 1175552	NM_001292063.2(OTOG):c.216+225_216+244del	OTOG	Deletion (intron variant)	not provided	GBenign
Select item 1223383	NM_001292063.2(OTOG):c.216+244T>A	OTOG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1273330	NM_001292063.2(OTOG):c.217-218G>A	OTOG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1675252	NM_001292063.2(OTOG):c.220G>A (p.Ala74Thr)	OTOG (A74T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 226872	NM_001292063.2(OTOG):c.237C>T (p.Ser79=)	OTOG	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2577823	NM_001292063.2(OTOG):c.238G>A (p.Val80Met)	OTOG (V80M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 930159	NM_001292063.2(OTOG):c.262C>T (p.Arg88Trp)	OTOG (R100W +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1331303	NM_001292063.2(OTOG):c.286C>G (p.Pro96Ala)	OTOG (P108A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 432317	NM_001292063.2(OTOG):c.292+4A>C	OTOG	Single nucleotide variant (intron variant)	Autosomal recessive nonsyndromic hearing loss 18B +2 more	GUncertain significance
Select item 226881	NM_001292063.2(OTOG):c.292+10A>T	OTOG	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1250160	NM_001292063.2(OTOG):c.292+127C>G	OTOG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1194971	NM_001292063.2(OTOG):c.292+165G>T	OTOG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1259881	NM_001292063.2(OTOG):c.293-294C>T	OTOG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237547	NM_001292063.2(OTOG):c.293-78T>C	OTOG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 496812	NM_001292063.2(OTOG):c.294C>G (p.Tyr98Ter)	OTOG (Y110* +1 more)	Single nucleotide variant (nonsense)	Autosomal recessive nonsyndromic hearing loss 18B +1 more	GPathogenic
Select item 1678833	NM_001292063.2(OTOG):c.310A>G (p.Asn104Asp)	OTOG (N104D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 229089	NM_001292063.2(OTOG):c.335C>G (p.Ala112Gly)	OTOG (A124G +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 2184145	NM_001292063.2(OTOG):c.353G>A (p.Arg118His)	OTOG (R130H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1327635	NM_001292063.2(OTOG):c.358A>G (p.Asn120Asp)	OTOG (N120D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 517609	NM_001292063.2(OTOG):c.371C>T (p.Pro124Leu)	OTOG (P136L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 229094	NM_001292063.2(OTOG):c.385G>A (p.Val129Met)	OTOG (V141M +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 18B +2 more	GConflicting classifications of pathogenicity
Select item 226893	NM_001292063.2(OTOG):c.385+7C>T	OTOG	Single nucleotide variant (intron variant)	Autosomal recessive nonsyndromic hearing loss 18B +2 more	GBenign
Select item 417886	NM_001292063.2(OTOG):c.397G>A (p.Gly133Ser)	OTOG (G145S +1 more)	Single nucleotide variant (missense variant)	Hearing impairment +2 more	GUncertain significance
Select item 930162	NM_001292063.2(OTOG):c.421C>T (p.Arg141Trp)	OTOG (R153W +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1207691	NM_001292063.2(OTOG):c.426G>A (p.Ala142=)	OTOG	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 817689	NM_001292063.2(OTOG):c.432del (p.Gln145fs)	OTOG (Q145fs +1 more)	Deletion (frameshift variant)	not provided	GPathogenic/Likely pathogenic
Select item 756460	NM_001292063.2(OTOG):c.441C>T (p.His147=)	OTOG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 517465	NM_001292063.2(OTOG):c.494C>A (p.Thr165Asn)	OTOG (T177N +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 228284	NM_001292063.2(OTOG):c.499del (p.Val167fs)	OTOG (V167fs)	Deletion (frameshift variant)	Rare genetic deafness +1 more	GPathogenic/Likely pathogenic
Select item 1185111	NM_001292063.2(OTOG):c.516C>T (p.Pro172=)	OTOG	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1704155	NM_001292063.2(OTOG):c.521_523del (p.Gly174_Gln175delinsGlu)	OTOG	Deletion (inframe_indel)	not provided	GUncertain significance
Select item 504777	NM_001292063.2(OTOG):c.534C>T (p.Ser178=)	OTOG	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1213497	NM_001292063.2(OTOG):c.540+173C>A	OTOG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1255018	NM_001292063.2(OTOG):c.541-241G>A	OTOG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1190392	NM_001292063.2(OTOG):c.541-133C>G	OTOG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1288918	NM_001292063.2(OTOG):c.541-103C>T	OTOG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235992	NM_001292063.2(OTOG):c.541-88G>A	OTOG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1190154	NM_001292063.2(OTOG):c.541-21G>A	OTOG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1297667	NM_001292063.2(OTOG):c.550G>A (p.Asp184Asn)	OTOG (D184N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3340790	NM_001292063.2(OTOG):c.554C>T (p.Pro185Leu)	OTOG (P185L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 680375	NM_001292063.2(OTOG):c.591T>G (p.Ala197=)	OTOG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 596372	NM_001292063.2(OTOG):c.600CTT[1] (p.Phe202del)	OTOG (F214del +1 more)	Microsatellite (inframe_deletion)	Autosomal recessive nonsyndromic hearing loss 18B +2 more	GUncertain significance
Select item 227791	NM_001292063.2(OTOG):c.639G>T (p.Glu213Asp)	OTOG (E225D +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign
Select item 1207537	NM_001292063.2(OTOG):c.659+23C>A	OTOG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1207117	NM_001292063.2(OTOG):c.659+210G>A	OTOG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1700410	NM_001292063.2(OTOG):c.661G>A (p.Val221Ile)	OTOG (V221I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1522841	NM_001292063.2(OTOG):c.680T>C (p.Met227Thr)	OTOG (M227T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 226906	NM_001292063.2(OTOG):c.688G>A (p.Ala230Thr)	OTOG (A242T +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 1683843	NM_001292063.2(OTOG):c.698A>G (p.Gln233Arg)	OTOG (Q233R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 226914	NM_001292063.2(OTOG):c.769G>A (p.Val257Ile)	OTOG (V269I +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 226924	NM_001292063.2(OTOG):c.843G>A (p.Lys281=)	OTOG	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1193719	NM_001292063.2(OTOG):c.866-295G>A	OTOG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1219973	NM_001292063.2(OTOG):c.866-81C>T	OTOG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2579516	NM_001292063.2(OTOG):c.873G>A (p.Leu291=)	OTOG	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 504778	NM_001292063.2(OTOG):c.879C>T (p.Asp293=)	OTOG	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 450925	NM_001292063.2(OTOG):c.883G>A (p.Val295Met)	OTOG (V307M +1 more)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 229109	NM_001292063.2(OTOG):c.899A>G (p.His300Arg)	OTOG (H312R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 226925	NM_001292063.2(OTOG):c.917C>A (p.Ala306Asp)	OTOG (A318D +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 1196554	NM_001292063.2(OTOG):c.920C>T (p.Pro307Leu)	OTOG (P307L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 500840	NM_001292063.2(OTOG):c.937C>A (p.Pro313Thr)	OTOG (P325T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 229110	NM_001292063.2(OTOG):c.938C>T (p.Pro313Leu)	OTOG (P325L +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1189209	NM_001292063.2(OTOG):c.966G>A (p.Pro322=)	OTOG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 226858	NM_001292063.2(OTOG):c.996+9C>A	OTOG	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1226002	NM_001292063.2(OTOG):c.996+78C>G	OTOG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 682654	NM_001292063.2(OTOG):c.997-35A>C	OTOG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1369784	NM_001292063.2(OTOG):c.1000G>A (p.Val334Met)	OTOG (V346M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 489156	NM_001292063.2(OTOG):c.1005C>G (p.Tyr335Ter)	OTOG (Y347* +1 more)	Single nucleotide variant (nonsense)	not provided	GLikely pathogenic
Select item 514533	NM_001292063.2(OTOG):c.1050C>T (p.His350=)	OTOG	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 226859	NM_001292063.2(OTOG):c.1059C>T (p.Val353=)	OTOG	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 226860	NM_001292063.2(OTOG):c.1087A>T (p.Thr363Ser)	OTOG (T375S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1268927	NM_001292063.2(OTOG):c.1104-164G>A	OTOG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253717	NM_001292063.2(OTOG):c.1104-68A>G	OTOG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 504779	NM_001292063.2(OTOG):c.1104-4A>C	OTOG	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 1033812	NM_001292063.2(OTOG):c.1148A>G (p.Tyr383Cys)	OTOG (Y383C +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

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