ClinVar for Gene (Select 3371) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3337674	NM_002160.4(TNC):c.1283G>T (p.Gly428Val)	TNC (G428V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3336965	NM_002160.4(TNC):c.3191C>T (p.Pro1064Leu)	TNC (P1064L)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 3336530	NM_002160.4(TNC):c.6051C>T (p.Thr2017=)	TNC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3336454	NM_002160.4(TNC):c.419G>A (p.Cys140Tyr)	TNC (C140Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3336355	NM_002160.4(TNC):c.1521C>A (p.Asn507Lys)	TNC (N507K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327448	NM_002160.4(TNC):c.3514G>C (p.Val1172Leu)	LOC126860741, TNC (V1172L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327447	NM_002160.4(TNC):c.3481T>C (p.Ser1161Pro)	TNC (S1161P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327446	NM_002160.4(TNC):c.635C>T (p.Thr212Met)	TNC (T212M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327445	NM_002160.4(TNC):c.2117C>T (p.Ala706Val)	TNC (A706V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327444	NM_002160.4(TNC):c.1969A>T (p.Thr657Ser)	TNC (T657S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327442	NM_002160.4(TNC):c.3293A>T (p.Asp1098Val)	TNC (D1098V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327441	NM_002160.4(TNC):c.6229C>T (p.Arg2077Trp)	TNC (R2077W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327440	NM_002160.4(TNC):c.3987G>T (p.Glu1329Asp)	TNC (E1329D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3327439	NM_002160.4(TNC):c.3488G>C (p.Gly1163Ala)	LOC126860741, TNC (G1163A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327438	NM_002160.4(TNC):c.6287A>C (p.Lys2096Thr)	TNC (K1914T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327437	NM_002160.4(TNC):c.2372G>A (p.Arg791Gln)	TNC (R791Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327436	NM_002160.4(TNC):c.3221C>T (p.Ala1074Val)	TNC (A1074V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327435	NM_002160.4(TNC):c.709A>C (p.Ile237Leu)	TNC (I237L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327434	NM_002160.4(TNC):c.1720G>A (p.Val574Met)	TNC (V574M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3327432	NM_002160.4(TNC):c.1610A>G (p.His537Arg)	TNC (H537R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3250407	NM_002160.4(TNC):c.323G>A (p.Arg108His)	TNC (R108H)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 56	GLikely pathogenic
Select item 3238904	NM_002160.4(TNC):c.608G>T (p.Gly203Val)	TNC (G203V)	Single nucleotide variant (missense variant)	Meniere disease +1 more	GConflicting classifications of pathogenicity
Select item 3238903	NM_002160.4(TNC):c.1873C>T (p.Pro625Ser)	TNC (P625S)	Single nucleotide variant (missense variant)	Meniere disease	GUncertain significance
Select item 3238902	NM_002160.4(TNC):c.2227G>A (p.Glu743Lys)	TNC (E743K)	Single nucleotide variant (missense variant)	Meniere disease	GUncertain significance
Select item 3238901	NM_002160.4(TNC):c.2512G>A (p.Gly838Ser)	TNC (G838S)	Single nucleotide variant (missense variant)	Meniere disease	GUncertain significance
Select item 3238900	NM_002160.4(TNC):c.2705T>A (p.Val902Asp)	TNC (V902D)	Single nucleotide variant (missense variant)	Meniere disease	GUncertain significance
Select item 3237485	NM_002160.4(TNC):c.4079G>A (p.Trp1360Ter)	TNC (W1269* +1 more)	Single nucleotide variant (nonsense)	Autosomal dominant nonsyndromic hearing loss 56	GUncertain significance
Select item 3234848	NM_002160.4(TNC):c.1973C>A (p.Pro658His)	TNC (P658H)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 56	GUncertain significance
Select item 3234325	NM_002160.4(TNC):c.3153C>A (p.Val1051=)	TNC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3180152	NM_002160.4(TNC):c.950A>G (p.Asn317Ser)	TNC (N317S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180151	NM_002160.4(TNC):c.860A>G (p.Asn287Ser)	TNC (N287S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180150	NM_002160.4(TNC):c.827G>A (p.Gly276Asp)	TNC (G276D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180149	NM_002160.4(TNC):c.718G>A (p.Glu240Lys)	TNC (E240K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180147	NM_002160.4(TNC):c.6235C>A (p.His2079Asn)	TNC (H2079N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180146	NM_002160.4(TNC):c.6179A>T (p.Asn2060Ile)	TNC (N2060I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180145	NM_002160.4(TNC):c.6177C>A (p.Asp2059Glu)	TNC (D2059E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180144	NM_002160.4(TNC):c.5915C>T (p.Thr1972Ile)	TNC (T1972I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180143	NM_002160.4(TNC):c.5672G>A (p.Arg1891Lys)	TNC (R1891K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180142	NM_002160.4(TNC):c.565G>A (p.Glu189Lys)	TNC (E189K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180141	NM_002160.4(TNC):c.5479G>T (p.Asp1827Tyr)	TNC (D1645Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180140	NM_002160.4(TNC):c.5345T>C (p.Met1782Thr)	TNC (M1600T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180139	NM_002160.4(TNC):c.5305C>T (p.Leu1769Phe)	TNC (L1587F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180138	NM_002160.4(TNC):c.5299G>T (p.Val1767Leu)	TNC (V1585L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180137	NM_002160.4(TNC):c.5239A>T (p.Ile1747Phe)	TNC (I1565F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180136	NM_002160.4(TNC):c.487G>T (p.Gly163Cys)	TNC (G163C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180135	NM_002160.4(TNC):c.4867G>A (p.Val1623Ile)	TNC (V1623I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180134	NM_002160.4(TNC):c.4547G>A (p.Arg1516Gln)	TNC (R1516Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180133	NM_002160.4(TNC):c.436T>C (p.Cys146Arg)	TNC (C146R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180132	NM_002160.4(TNC):c.4366C>G (p.Leu1456Val)	TNC (L1456V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180131	NM_002160.4(TNC):c.4310A>G (p.Lys1437Arg)	TNC (K1346R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180130	NM_002160.4(TNC):c.4048C>G (p.Leu1350Val)	TNC (L1350V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180129	NM_002160.4(TNC):c.4018G>A (p.Val1340Ile)	TNC (V1340I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3180127	NM_002160.4(TNC):c.3791T>C (p.Val1264Ala)	TNC (V1264A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3180126	NM_002160.4(TNC):c.3773A>G (p.Asp1258Gly)	LOC126860741, TNC (D1258G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3180125	NM_002160.4(TNC):c.3322G>A (p.Val1108Met)	TNC (V1108M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180124	NM_002160.4(TNC):c.2986A>T (p.Thr996Ser)	TNC (T996S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180123	NM_002160.4(TNC):c.2968G>A (p.Asp990Asn)	TNC (D990N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180122	NM_002160.4(TNC):c.2941G>A (p.Ala981Thr)	TNC (A981T)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 56 +1 more	GConflicting classifications of pathogenicity
Select item 3180121	NM_002160.4(TNC):c.2734G>C (p.Glu912Gln)	TNC (E912Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180120	NM_002160.4(TNC):c.2600C>T (p.Thr867Ile)	TNC (T867I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180119	NM_002160.4(TNC):c.2536C>T (p.Arg846Cys)	TNC (R846C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180118	NM_002160.4(TNC):c.235C>A (p.Pro79Thr)	TNC (P79T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180117	NM_002160.4(TNC):c.2129C>T (p.Thr710Met)	TNC (T710M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180116	NM_002160.4(TNC):c.2006G>A (p.Arg669His)	TNC (R669H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180115	NM_002160.4(TNC):c.2005C>T (p.Arg669Cys)	TNC (R669C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180114	NM_002160.4(TNC):c.1526G>A (p.Gly509Asp)	TNC (G509D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180113	NM_002160.4(TNC):c.1343G>A (p.Arg448His)	TNC (R448H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3068984	NM_002160.4(TNC):c.5722C>T (p.Arg1908Ter)	TNC (R1726* +1 more)	Single nucleotide variant (nonsense)	not specified	GUncertain significance
Select item 3063071	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3	DMAC1, DMRT1 +769 more	Copy number gain	not specified	GPathogenic
Select item 3059146	NM_002160.4(TNC):c.6073-4A>G	TNC	Single nucleotide variant (intron variant)	TNC-related disorder	GLikely benign
Select item 3058124	NM_002160.4(TNC):c.2673A>C (p.Thr891=)	TNC	Single nucleotide variant (synonymous variant)	TNC-related disorder	GLikely benign
Select item 3051376	NM_002160.4(TNC):c.3889G>A (p.Glu1297Lys)	TNC (E1297K)	Single nucleotide variant (missense variant +1 more)	TNC-related disorder	GUncertain significance
Select item 3049502	NM_002160.4(TNC):c.2607C>T (p.Tyr869=)	TNC	Single nucleotide variant (synonymous variant)	TNC-related disorder	GLikely benign
Select item 3047924	NM_002160.4(TNC):c.3810T>C (p.Asp1270=)	TNC	Single nucleotide variant (synonymous variant +1 more)	TNC-related disorder	GLikely benign
Select item 3046731	NM_002160.4(TNC):c.98G>A (p.Arg33Gln)	TNC (R33Q)	Single nucleotide variant (missense variant)	TNC-related disorder	GLikely benign
Select item 3046251	NM_002160.4(TNC):c.4383C>T (p.Thr1461=)	TNC	Single nucleotide variant (synonymous variant)	TNC-related disorder	GLikely benign
Select item 3045851	NM_002160.4(TNC):c.2951-9T>C	TNC	Single nucleotide variant (intron variant)	TNC-related disorder	GLikely benign
Select item 3044631	NM_002160.4(TNC):c.3285C>T (p.Thr1095=)	TNC	Single nucleotide variant (synonymous variant)	TNC-related disorder	GLikely benign
Select item 3043582	NM_002160.4(TNC):c.5731C>T (p.Arg1911Trp)	TNC (R1729W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3042847	NM_002160.4(TNC):c.2448C>T (p.Asp816=)	TNC	Single nucleotide variant (synonymous variant)	TNC-related disorder	GLikely benign
Select item 3042846	NM_002160.4(TNC):c.2463C>T (p.Ile821=)	TNC	Single nucleotide variant (synonymous variant)	TNC-related disorder	GLikely benign
Select item 3040413	NM_002160.4(TNC):c.5222G>A (p.Arg1741Gln)	TNC (R1559Q +1 more)	Single nucleotide variant (missense variant)	TNC-related disorder	GLikely benign
Select item 3039169	NM_002160.4(TNC):c.6593G>A (p.Arg2198His)	TNC (R2016H +1 more)	Single nucleotide variant (missense variant)	TNC-related disorder	GLikely benign
Select item 3039084	NM_002160.4(TNC):c.4866A>G (p.Glu1622=)	TNC	Single nucleotide variant (synonymous variant)	TNC-related disorder	GLikely benign
Select item 3038409	NM_002160.4(TNC):c.2442C>T (p.Val814=)	TNC	Single nucleotide variant (synonymous variant)	TNC-related disorder	GLikely benign
Select item 3034137	NM_002160.4(TNC):c.4076G>A (p.Gly1359Asp)	TNC (G1268D +1 more)	Single nucleotide variant (missense variant)	TNC-related disorder	GLikely benign
Select item 3033882	NM_002160.4(TNC):c.2813T>C (p.Val938Ala)	TNC (V938A)	Single nucleotide variant (missense variant)	TNC-related disorder	GLikely benign
Select item 3032422	NM_002160.4(TNC):c.194C>T (p.Ser65Leu)	TNC (S65L)	Single nucleotide variant (missense variant)	TNC-related disorder	GLikely benign
Select item 3031013	NM_002160.4(TNC):c.3926G>A (p.Arg1309His)	TNC (R1309H)	Single nucleotide variant (missense variant +1 more)	TNC-related disorder	GLikely benign
Select item 3029468	NM_002160.4(TNC):c.3299C>T (p.Ala1100Val)	TNC (A1100V)	Single nucleotide variant (missense variant)	TNC-related disorder	GUncertain significance
Select item 2775398	NM_002160.4(TNC):c.5247A>T (p.Gly1749=)	TNC	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 56	GPathogenic
Select item 2683060	NM_002160.4(TNC):c.5845A>G (p.Thr1949Ala)	TNC (T1767A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2682303	NM_002160.4(TNC):c.5758G>T (p.Val1920Phe)	TNC (V1738F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2673188	NM_002160.4(TNC):c.5978C>T (p.Thr1993Met)	TNC (T1811M +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2664067	NM_002160.4(TNC):c.2192A>C (p.Glu731Ala)	TNC (E731A)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 56	GUncertain significance
Select item 2659459	NM_002160.4(TNC):c.867C>T (p.Tyr289=)	TNC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2659458	NM_002160.4(TNC):c.2860+3G>A	TNC	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 2659457	NM_002160.4(TNC):c.3140A>G (p.Gln1047Arg)	TNC (Q1047R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2659456	NM_002160.4(TNC):c.3352C>T (p.Arg1118Trp)	TNC (R1118W)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2659455	NM_002160.4(TNC):c.3637G>A (p.Val1213Ile)	LOC126860741, TNC (V1213I)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity

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