ClinVar for MedGen (Select 321902) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3075725	NM_005422.4(TECTA):c.568A>C (p.Thr190Pro)	TBCEL-TECTA, TECTA (T190P +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GLikely pathogenic
Select item 2581039	NM_005422.4(TECTA):c.140C>G (p.Ser47Cys)	TBCEL-TECTA, TECTA (S366C +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GUncertain significance
Select item 2441893	NM_005422.4(TECTA):c.5515G>A (p.Gly1839Ser)	TBCEL-TECTA, TECTA (G1839S +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 2441747	NM_005422.4(TECTA):c.1316T>C (p.Phe439Ser)	TECTA, TBCEL-TECTA (F439S +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GUncertain significance
Select item 2137273	NM_005422.4(TECTA):c.4690-1G>A	TBCEL-TECTA, TECTA	Single nucleotide variant (splice acceptor variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GPathogenic/Likely pathogenic
Select item 1710226	NM_005422.4(TECTA):c.3156G>T (p.Trp1052Cys)	TBCEL-TECTA, TECTA (W1052C +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GUncertain significance
Select item 1708127	NM_005422.4(TECTA):c.1115dup (p.Ser373fs)	TBCEL-TECTA, TECTA (S373fs +1 more)	Duplication (frameshift variant)	Autosomal dominant nonsyndromic hearing loss 12	GPathogenic
Select item 1705575	NM_005422.4(TECTA):c.493A>T (p.Thr165Ser)	TBCEL-TECTA, TECTA (T165S +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GUncertain significance
Select item 1345003	NM_005422.4(TECTA):c.1391A>G (p.Tyr464Cys)	TBCEL-TECTA, TECTA (Y783C +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1333705	NM_005422.4(TECTA):c.2012G>A (p.Cys671Tyr)	TBCEL-TECTA, TECTA (C671Y +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GUncertain significance
Select item 1329694	NM_005422.4(TECTA):c.102del (p.Asn34fs)	TBCEL-TECTA, TECTA (N34fs +1 more)	Deletion (frameshift variant)	Autosomal dominant nonsyndromic hearing loss 12 +2 more	GPathogenic/Likely pathogenic
Select item 1329482	NM_005422.4(TECTA):c.1690C>T (p.Leu564Phe)	TBCEL-TECTA, TECTA (L564F +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GUncertain significance
Select item 1314648	NM_005422.4(TECTA):c.4180C>A (p.Leu1394Met)	TBCEL-TECTA, TECTA (L1394M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1274473	NM_005422.4(TECTA):c.5586+40C>G	TBCEL-TECTA, TECTA	Single nucleotide variant (intron variant)	Autosomal dominant nonsyndromic hearing loss 12 +2 more	GBenign
Select item 1185582	NM_005422.4(TECTA):c.5383+5_5383+8del	TBCEL-TECTA, TECTA	Microsatellite (splice donor variant)	not provided +2 more	GPathogenic
Select item 1177853	NM_005422.4(TECTA):c.5272+26A>G	TBCEL-TECTA, TECTA	Single nucleotide variant (intron variant)	Autosomal dominant nonsyndromic hearing loss 12 +2 more	GBenign
Select item 1034177	NM_005422.4(TECTA):c.761T>C (p.Ile254Thr)	TBCEL-TECTA, TECTA (I573T +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GUncertain significance
Select item 1034175	NM_005422.4(TECTA):c.2848G>A (p.Glu950Lys)	LOC126861365, TBCEL-TECTA +1 more (E950K +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GUncertain significance
Select item 1032996	NM_005422.4(TECTA):c.1472G>T (p.Arg491Leu)	TBCEL-TECTA, TECTA (R491L +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GUncertain significance
Select item 1028888	NM_005422.4(TECTA):c.4494C>A (p.Phe1498Leu)	TBCEL-TECTA, TECTA (F1498L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1027366	NM_005422.4(TECTA):c.5510G>A (p.Cys1837Tyr)	TBCEL-TECTA, TECTA (C1837Y +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GLikely pathogenic
Select item 932015	NM_005422.4(TECTA):c.4932C>A (p.Ser1644Arg)	TBCEL-TECTA, TECTA (S1963R +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GUncertain significance
Select item 930525	NM_005422.4(TECTA):c.6061C>T (p.Arg2021Cys)	TBCEL-TECTA, TECTA (R2021C +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GConflicting classifications of pathogenicity
Select item 930247	NM_005422.4(TECTA):c.2644G>A (p.Glu882Lys)	LOC126861365, TBCEL-TECTA +1 more (E882K +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 880464	NM_005422.4(TECTA):c.3126G>A (p.Gly1042=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 21 +2 more	GConflicting classifications of pathogenicity
Select item 880382	NM_005422.4(TECTA):c.1651G>A (p.Val551Met)	TBCEL-TECTA, TECTA (V551M)	Single nucleotide variant (missense variant)	TECTA-related disorder +4 more	GConflicting classifications of pathogenicity
Select item 880300	NM_005422.4(TECTA):c.420T>C (p.Ser140=)	TECTA, TBCEL-TECTA	Single nucleotide variant (synonymous variant)	not provided +2 more	GUncertain significance
Select item 880299	NM_005422.4(TECTA):c.377C>T (p.Thr126Ile)	TBCEL-TECTA, TECTA (T126I)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 879825	NM_005422.4(TECTA):c.5877G>C (p.Leu1959=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 879786	NM_005422.4(TECTA):c.5260A>G (p.Lys1754Glu)	TBCEL-TECTA, TECTA (K1754E)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 21 +1 more	GUncertain significance
Select item 879785	NM_005422.4(TECTA):c.5205C>T (p.Ala1735=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 21 +2 more	GConflicting classifications of pathogenicity
Select item 879734	NM_005422.4(TECTA):c.4594G>A (p.Asp1532Asn)	TBCEL-TECTA, TECTA (D1532N)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +2 more	GConflicting classifications of pathogenicity
Select item 879402	NM_005422.4(TECTA):c.5142C>T (p.Tyr1714=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	TECTA-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 879283	NM_005422.4(TECTA):c.2889C>A (p.Ala963=)	LOC126861365, TBCEL-TECTA +1 more	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 21 +1 more	GUncertain significance
Select item 879227	NM_005422.4(TECTA):c.2327A>T (p.Gln776Leu)	TBCEL-TECTA, TECTA (Q776L)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 879177	NM_005422.4(TECTA):c.1498G>A (p.Asp500Asn)	TBCEL-TECTA, TECTA (D500N)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 879127	NM_005422.4(TECTA):c.880T>C (p.Cys294Arg)	TBCEL-TECTA, TECTA (C294R)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 879126	NM_005422.4(TECTA):c.850C>T (p.Arg284Cys)	TBCEL-TECTA, TECTA (R284C)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 879125	NM_005422.4(TECTA):c.805C>G (p.Arg269Gly)	TBCEL-TECTA, TECTA (R269G)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 21 +1 more	GConflicting classifications of pathogenicity
Select item 878823	NM_005422.4(TECTA):c.5046C>T (p.Ile1682=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 878772	NM_005422.4(TECTA):c.4295A>G (p.Lys1432Arg)	TBCEL-TECTA, TECTA (K1432R)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +2 more	GConflicting classifications of pathogenicity
Select item 878729	NM_005422.4(TECTA):c.3575A>C (p.Lys1192Thr)	TBCEL-TECTA, TECTA (K1192T)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 878628	NM_005422.4(TECTA):c.2222A>G (p.Lys741Arg)	TBCEL-TECTA, TECTA (K741R)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 878627	NM_005422.4(TECTA):c.2175C>T (p.Asp725=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 878535	NM_005422.4(TECTA):c.714C>T (p.Asn238=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 12 +2 more	GConflicting classifications of pathogenicity
Select item 878052	NM_005422.4(TECTA):c.6150C>T (p.Tyr2050=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 877889	NM_005422.4(TECTA):c.6069C>T (p.His2023=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 877888	NM_005422.4(TECTA):c.5878T>C (p.Tyr1960His)	TBCEL-TECTA, TECTA (Y1960H)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 877844	NM_005422.4(TECTA):c.5577C>T (p.Asn1859=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 877843	NM_005422.4(TECTA):c.5362G>A (p.Glu1788Lys)	TBCEL-TECTA, TECTA (E1788K)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 877779	NM_005422.4(TECTA):c.4901T>C (p.Val1634Ala)	TBCEL-TECTA, TECTA (V1634A)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 877738	NM_005422.4(TECTA):c.4168G>A (p.Ala1390Thr)	TECTA, TBCEL-TECTA (A1390T)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 877662	NM_005422.4(TECTA):c.2674C>A (p.Leu892Met)	LOC126861365, TBCEL-TECTA +1 more (L892M)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 877562	NM_005422.4(TECTA):c.1143C>G (p.Leu381=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 877561	NM_005422.4(TECTA):c.1089G>T (p.Val363=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 877514	NM_005422.4(TECTA):c.552C>T (p.Tyr184=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 12 +3 more	GConflicting classifications of pathogenicity
Select item 872040	NM_005422.4(TECTA):c.4163G>A (p.Arg1388His)	TBCEL-TECTA, TECTA (R1388H)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 21 +2 more	GConflicting classifications of pathogenicity
Select item 869465	NM_005422.4(TECTA):c.5539T>C (p.Ser1847Pro)	TBCEL-TECTA, TECTA (S1847P)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GLikely pathogenic
Select item 869464	NM_005422.4(TECTA):c.1796G>C (p.Ser599Thr)	TBCEL-TECTA, TECTA (S599T)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 742069	NM_005422.4(TECTA):c.4317A>C (p.Leu1439=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 689604	NM_005422.4(TECTA):c.29G>C (p.Trp10Ser)	TBCEL-TECTA, TECTA (W10S +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12	GLikely benign
Select item 689602	NM_005422.4(TECTA):c.5488G>A (p.Val1830Met)	TBCEL-TECTA, TECTA (V1830M +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GConflicting classifications of pathogenicity
Select item 667171	NM_005422.4(TECTA):c.90A>T (p.Pro30=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 667169	NM_005422.4(TECTA):c.2700G>A (p.Ser900=)	LOC126861365, TBCEL-TECTA +1 more	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 21 +3 more	GConflicting classifications of pathogenicity
Select item 667166	NM_005422.4(TECTA):c.33C>A (p.Val11=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 21 +4 more	GConflicting classifications of pathogenicity
Select item 631653	NM_005422.4(TECTA):c.4402G>T (p.Glu1468Ter)	TBCEL-TECTA, TECTA (E1468* +1 more)	Single nucleotide variant (nonsense)	Autosomal dominant nonsyndromic hearing loss 12	GUncertain significance
Select item 546450	NM_005422.4(TECTA):c.458C>T (p.Thr153Met)	TBCEL-TECTA, TECTA (T153M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 502103	NM_005422.4(TECTA):c.2088C>T (p.Cys696=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 498538	NM_005422.4(TECTA):c.4085G>A (p.Trp1362Ter)	TBCEL-TECTA, TECTA (W1362* +1 more)	Single nucleotide variant (nonsense)	Nonsyndromic genetic hearing loss	GPathogenic FDA Recognized database
Select item 444275	NM_005422.4(TECTA):c.6100G>A (p.Asp2034Asn)	TBCEL-TECTA, TECTA (D2034N +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +2 more	GUncertain significance
Select item 429887	NM_005422.4(TECTA):c.4061C>T (p.Thr1354Ile)	TBCEL-TECTA, TECTA (T1354I +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 21 +2 more	GConflicting classifications of pathogenicity
Select item 417919	NM_005422.4(TECTA):c.3854G>C (p.Cys1285Ser)	TBCEL-TECTA, TECTA (C1285S +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 403527	NM_005422.4(TECTA):c.3743C>T (p.Pro1248Leu)	TBCEL-TECTA, TECTA (P1248L +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 21 +4 more	GConflicting classifications of pathogenicity
Select item 303047	NM_005422.4(TECTA):c.6458C>T (p.Thr2153Met)	TBCEL-TECTA, TECTA (T2153M +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 303046	NM_005422.4(TECTA):c.6428C>T (p.Ser2143Leu)	TBCEL-TECTA, TECTA (S2143L +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 303045	NM_005422.4(TECTA):c.6301C>T (p.Arg2101Trp)	TBCEL-TECTA, TECTA (R2101W +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 303044	NM_005422.4(TECTA):c.6136G>A (p.Asp2046Asn)	TBCEL-TECTA, TECTA (D2046N +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +2 more	GConflicting classifications of pathogenicity
Select item 303043	NM_005422.4(TECTA):c.6135C>T (p.Cys2045=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 303042	NM_005422.4(TECTA):c.5913A>T (p.Thr1971=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 303041	NM_005422.4(TECTA):c.5908G>A (p.Ala1970Thr)	TBCEL-TECTA, TECTA (A1970T +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GConflicting classifications of pathogenicity
Select item 303040	NM_005422.4(TECTA):c.5829A>G (p.Lys1943=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 303039	NM_005422.4(TECTA):c.5770C>A (p.Pro1924Thr)	TBCEL-TECTA, TECTA (P1924T +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 303038	NM_005422.4(TECTA):c.5743A>C (p.Met1915Leu)	TBCEL-TECTA, TECTA (M1915L +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 303037	NM_005422.4(TECTA):c.5587-15C>G	TBCEL-TECTA, TECTA	Single nucleotide variant (intron variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 303036	NM_005422.4(TECTA):c.5586+12A>G	TBCEL-TECTA, TECTA	Single nucleotide variant (intron variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 303035	NM_005422.4(TECTA):c.5583G>T (p.Val1861=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 303034	NM_005422.4(TECTA):c.5550C>G (p.Ile1850Met)	TBCEL-TECTA, TECTA (I1850M +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 303033	NM_005422.4(TECTA):c.5496C>G (p.Ile1832Met)	TBCEL-TECTA, TECTA (I1832M +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 303032	NM_005422.4(TECTA):c.5114A>G (p.Tyr1705Cys)	TECTA, TBCEL-TECTA (Y1705C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 303031	NM_005422.4(TECTA):c.5091G>A (p.Met1697Ile)	TBCEL-TECTA, TECTA (M1697I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 303030	NM_005422.4(TECTA):c.4977-12C>T	TBCEL-TECTA, TECTA	Single nucleotide variant (intron variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 303029	NM_005422.4(TECTA):c.4965C>T (p.Gly1655=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 303028	NM_005422.4(TECTA):c.4842G>C (p.Leu1614=)	TBCEL-TECTA, TECTA	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 21 +1 more	GUncertain significance
Select item 303027	NM_005422.4(TECTA):c.4720A>G (p.Ile1574Val)	TBCEL-TECTA, TECTA (I1574V +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 21 +5 more	GConflicting classifications of pathogenicity
Select item 303026	NM_005422.4(TECTA):c.4441A>G (p.Ser1481Gly)	TBCEL-TECTA, TECTA (S1481G +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 303025	NM_005422.4(TECTA):c.4337C>G (p.Thr1446Arg)	TBCEL-TECTA, TECTA (T1446R +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 303024	NM_005422.4(TECTA):c.4289A>G (p.Asp1430Gly)	TBCEL-TECTA, TECTA (D1430G +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 303023	NM_005422.4(TECTA):c.4205G>C (p.Cys1402Ser)	TBCEL-TECTA, TECTA (C1402S +1 more)	Single nucleotide variant (missense variant)	Meniere disease +3 more	GUncertain significance
Select item 303022	NM_005422.4(TECTA):c.4061C>G (p.Thr1354Ser)	TBCEL-TECTA, TECTA (T1354S +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance
Select item 303020	NM_005422.4(TECTA):c.3760A>G (p.Met1254Val)	TBCEL-TECTA, TECTA (M1254V +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 12 +1 more	GUncertain significance

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