"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "OTOF"[g - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1355112	NM_194323.3(OTOF):c.3631A>T (p.Met1211Leu)	OTOF (M1211L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 180120	NM_194323.3(OTOF):c.3624del (p.Leu1209fs)	OTOF (L1976fs +1 more)	Deletion (frameshift variant +1 more)	Nonsyndromic genetic hearing loss +2 more	GPathogenic/Likely pathogenic
Select item 178626	NM_194323.3(OTOF):c.3621G>A (p.Leu1207=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	Autosomal recessive nonsyndromic hearing loss 9 +2 more	GConflicting classifications of pathogenicity
Select item 2903336	NM_194323.3(OTOF):c.3615G>A (p.Ala1205=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1254040	NM_194323.3(OTOF):c.3522C>T (p.Asp1174=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 548986	NM_194323.3(OTOF):c.3515G>A (p.Arg1172Gln)	OTOF (R1939Q +1 more)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 9 +3 more	GPathogenic
Select item 562079	NM_194323.3(OTOF):c.3514C>T (p.Arg1172Trp)	OTOF (R1172W +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2832378	NM_194248.3(OTOF):c.*18-18CT[2]	OTOF	Microsatellite (intron variant)	not provided	GLikely benign
Select item 667143	NM_194248.3(OTOF):c.5991C>T (p.Ala1997=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GBenign/Likely benign
Select item 2175181	NM_194248.3(OTOF):c.5985C>T (p.Leu1995=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2860795	NM_194248.3(OTOF):c.5970G>A (p.Leu1990=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2988827	NM_194248.3(OTOF):c.5967C>T (p.Tyr1989=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1532499	NM_194248.3(OTOF):c.5958G>C (p.Val1986=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2835351	NM_194248.3(OTOF):c.5952C>T (p.Tyr1984=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3004583	NM_194248.3(OTOF):c.5943G>A (p.Leu1981=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2796799	NM_194248.3(OTOF):c.5941C>T (p.Leu1981=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2794433	NM_194248.3(OTOF):c.5940C>G (p.Ala1980=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1970292	NM_194248.3(OTOF):c.5940C>T (p.Ala1980=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 417910	NM_194248.3(OTOF):c.5938G>T (p.Ala1980Ser)	OTOF (A1980S +2 more)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 9 +2 more	GConflicting classifications of pathogenicity
Select item 2914418	NM_194248.3(OTOF):c.5937C>T (p.Leu1979=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3012393	NM_194248.3(OTOF):c.5928C>G (p.Leu1976=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2694832	NM_194248.3(OTOF):c.5917C>T (p.Leu1973=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2979157	NM_194248.3(OTOF):c.5916C>T (p.Leu1972=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2698575	NM_194248.3(OTOF):c.5907G>A (p.Leu1969=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1958401	NM_194248.3(OTOF):c.5907G>C (p.Leu1969=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2746694	NM_194248.3(OTOF):c.5904A>G (p.Lys1968=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1497506	NM_194248.3(OTOF):c.5903A>G (p.Lys1968Arg)	OTOF (K1278R +2 more)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 9 +1 more	GUncertain significance
Select item 2972996	NM_194248.3(OTOF):c.5892G>A (p.Trp1964Ter)	OTOF (W1274* +2 more)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 3017824	NM_194248.3(OTOF):c.5883G>A (p.Thr1961=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2860764	NM_194248.3(OTOF):c.5868C>A (p.Tyr1956Ter)	OTOF (Y1266* +2 more)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 2434523	NM_194248.3(OTOF):c.5864G>A (p.Arg1955His)	OTOF (R1188H +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2989686	NM_194248.3(OTOF):c.5859G>A (p.Ser1953=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2896347	NM_194248.3(OTOF):c.5859G>T (p.Ser1953=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2807727	NM_194248.3(OTOF):c.5814-1_5833del	OTOF	Deletion (intron variant +1 more)	not provided	GPathogenic
Select item 593393	NM_194248.3(OTOF):c.5829C>T (p.Ser1943=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GConflicting classifications of pathogenicity
Select item 48272	NM_194248.3(OTOF):c.5826G>A (p.Thr1942=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GBenign/Likely benign
Select item 739187	NM_194248.3(OTOF):c.5820C>T (p.Pro1940=)	OTOF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 6136	NM_194248.3(OTOF):c.5816G>A (p.Arg1939Gln)	OTOF (R1939Q +2 more)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 9 +1 more	GPathogenic/Likely pathogenic
Select item 65813	NM_194248.3(OTOF):c.5815C>T (p.Arg1939Trp)	OTOF (R1939W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3012694	NM_194248.3(OTOF):c.5814-6C>T	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2183925	NM_194248.3(OTOF):c.5814-7A>T	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2814353	NM_194248.3(OTOF):c.5814-8T>C	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2970825	NM_194248.3(OTOF):c.5814-9A>G	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2859248	NM_194248.3(OTOF):c.5814-13C>T	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2979075	NM_194248.3(OTOF):c.5814-14C>A	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2966232	NM_194248.3(OTOF):c.5814-17T>C	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2986413	NM_194248.3(OTOF):c.5814-20dup	OTOF	Duplication (intron variant)	not provided	GLikely benign
Select item 2739502	NM_194248.3(OTOF):c.5814-20C>T	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 48270	NM_194248.3(OTOF):c.5813+15G>A	OTOF	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 2955302	NM_194248.3(OTOF):c.5813+14C>T	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 514686	NM_194248.3(OTOF):c.5813+9C>T	OTOF	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 2995297	NM_194248.3(OTOF):c.5812_5813+2del	OTOF	Deletion (splice donor variant)	not provided	GLikely pathogenic
Select item 65812	NM_194248.3(OTOF):c.5800dup (p.Leu1934fs)	OTOF (L1934fs +2 more)	Duplication (frameshift variant)	Bilateral sensorineural hearing impairment +2 more	GPathogenic/Likely pathogenic
Select item 1969296	NM_194248.3(OTOF):c.5776C>A (p.Leu1926Met)	OTOF (L1236M +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2857248	NM_194248.3(OTOF):c.5772G>A (p.Val1924=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2825152	NM_194248.3(OTOF):c.5766C>T (p.Asn1922=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2772982	NM_194248.3(OTOF):c.5745A>C (p.Thr1915=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 48269	NM_194248.3(OTOF):c.5742G>A (p.Leu1914=)	OTOF	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2778690	NM_194248.3(OTOF):c.5740C>T (p.Leu1914=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2902169	NM_194248.3(OTOF):c.5727T>A (p.Ala1909=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2902969	NM_194248.3(OTOF):c.5718G>A (p.Lys1906=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 48268	NM_194248.3(OTOF):c.5713-2A>G	OTOF	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 2906877	NM_194248.3(OTOF):c.5713-6C>T	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1603127	NM_194248.3(OTOF):c.5713-16T>A	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2835338	NM_194248.3(OTOF):c.5713-18C>A	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1672656	NM_194248.3(OTOF):c.5712+20C>T	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2748908	NM_194248.3(OTOF):c.5712+7_5712+18del	OTOF	Deletion (intron variant)	not provided	GLikely benign
Select item 3010312	NM_194248.3(OTOF):c.5712+16T>C	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2747208	NM_194248.3(OTOF):c.5712+15C>T	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2985265	NM_194248.3(OTOF):c.5712+14C>T	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2877844	NM_194248.3(OTOF):c.5712+11dup	OTOF	Duplication (intron variant)	not provided	GBenign
Select item 2835187	NM_194248.3(OTOF):c.5712+8C>A	OTOF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 48267	NM_194248.3(OTOF):c.5712+6C>G	OTOF	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1478440	NM_194248.3(OTOF):c.5712+5G>A	OTOF	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1425927	NM_194248.3(OTOF):c.5711C>T (p.Thr1904Met)	OTOF (T1137M +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2782958	NM_194248.3(OTOF):c.5703T>C (p.Phe1901=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2781298	NM_194248.3(OTOF):c.5700G>A (p.Glu1900=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2870016	NM_194248.3(OTOF):c.5697T>C (p.Asp1899=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 681381	NM_194248.3(OTOF):c.5694C>T (p.Asn1898=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2069466	NM_194248.3(OTOF):c.5684G>A (p.Arg1895His)	OTOF (R1128H +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2729691	NM_194248.3(OTOF):c.5682C>G (p.Ala1894=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2107142	NM_194248.3(OTOF):c.5674C>A (p.Leu1892Ile)	OTOF (L1202I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2962559	NM_194248.3(OTOF):c.5673C>T (p.Pro1891=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2501018	NM_194248.3(OTOF):c.5667G>A (p.Trp1889Ter)	OTOF (W1122* +2 more)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 2748665	NM_194248.3(OTOF):c.5661del (p.Gly1888fs)	OTOF (G1121fs +2 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2748667	NM_194248.3(OTOF):c.5658C>G (p.Val1886=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 21858	NM_194248.3(OTOF):c.5655C>T (p.Arg1885=)	OTOF	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 9 +2 more	GBenign/Likely benign
Select item 3007422	NM_194248.3(OTOF):c.5652G>A (p.Lys1884=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2809523	NM_194248.3(OTOF):c.5646G>A (p.Lys1882=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2957269	NM_194248.3(OTOF):c.5634G>A (p.Val1878=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 391704	NM_194248.3(OTOF):c.5632G>A (p.Val1878Met)	OTOF (V1878M +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2999902	NM_194248.3(OTOF):c.5631C>T (p.Leu1877=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2982633	NM_194248.3(OTOF):c.5628C>T (p.Pro1876=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 335429	NM_194248.3(OTOF):c.5623G>A (p.Val1875Met)	OTOF (V1875M +2 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 9 +1 more	GConflicting classifications of pathogenicity
Select item 2893173	NM_194248.3(OTOF):c.5622C>T (p.Asp1874=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3016691	NM_194248.3(OTOF):c.5616G>A (p.Glu1872=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2827154	NM_194248.3(OTOF):c.5613G>A (p.Gly1871=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 48265	NM_194248.3(OTOF):c.5610C>T (p.Thr1870=)	OTOF	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2832506	NM_194248.3(OTOF):c.5595C>T (p.Thr1865=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2698870	NM_194248.3(OTOF):c.5586G>A (p.Lys1862=)	OTOF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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