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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59123	GRCh38/hg38 9q22.33-33.1(chr9:99349916-115767475)x1	CT70, CTNNAL1 +509 more	Copy number loss	See cases	GPathogenic
Select item 805677	NM_002160.4(TNC):c.6499G>A (p.Val2167Ile)	TNC (V2167I)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 56 +1 more	GBenign/Likely benign
Select item 1243437	NM_002160.4(TNC):c.6496-6del	TNC	Deletion (intron variant)	not provided	GBenign
Select item 1316716	NM_002160.4(TNC):c.6496-38CT[10]	TNC	Microsatellite (intron variant)	not provided	GLikely benign
Select item 720440	NM_002160.4(TNC):c.6482A>G (p.Asn2161Ser)	TNC (N2161S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1288564	NM_002160.4(TNC):c.6332-93C>T	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316983	NM_002160.4(TNC):c.6273C>T (p.Ser2091=)	TNC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1315734	NM_002160.4(TNC):c.6230G>A (p.Arg2077Gln)	TNC (R2077Q)	Single nucleotide variant (missense variant)	not specified +1 more	GLikely benign
Select item 1296879	NM_002160.4(TNC):c.6170-28C>T	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316783	NM_002160.4(TNC):c.6169+255G>A	TNC	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1320576	NM_002160.4(TNC):c.6169+233A>T	TNC	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1317855	NM_002160.4(TNC):c.6169+127C>G	TNC	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1221829	NM_002160.4(TNC):c.6169+22A>G	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 586836	NM_002160.4(TNC):c.6144G>A (p.Gly2048=)	TNC	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 56 +1 more	GBenign
Select item 776444	NM_002160.4(TNC):c.6099C>T (p.Arg2033=)	TNC	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1262996	NM_002160.4(TNC):c.6072+272del	TNC	Deletion (intron variant)	not provided	GBenign
Select item 1263677	NM_002160.4(TNC):c.6072+259C>G	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266236	NM_002160.4(TNC):c.6072+107C>A	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316870	NM_002160.4(TNC):c.6072+90G>A	TNC	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1259794	NM_002160.4(TNC):c.6022G>C (p.Glu2008Gln)	TNC (E2008Q)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 784149	NM_002160.4(TNC):c.6006G>A (p.Leu2002=)	TNC	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 56 +1 more	GBenign/Likely benign
Select item 1180026	NM_002160.4(TNC):c.5921-192T>A	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281524	NM_002160.4(TNC):c.5920+175G>A	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1315921	NM_002160.4(TNC):c.5810C>T (p.Thr1937Ile)	TNC (T1937I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1283615	NM_002160.4(TNC):c.5788-190C>T	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267735	NM_002160.4(TNC):c.5787+114dup	TNC	Duplication (intron variant)	not provided	GBenign
Select item 1270129	NM_002160.4(TNC):c.5787+89C>T	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 789777	NM_002160.4(TNC):c.5745C>A (p.Thr1915=)	TNC	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 56 +1 more	GBenign
Select item 1317268	NM_002160.4(TNC):c.5700G>A (p.Ser1900=)	TNC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1182259	NM_002160.4(TNC):c.5673A>G (p.Arg1891=)	TNC	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 748717	NM_002160.4(TNC):c.5657-9C>T	TNC	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1318359	NM_002160.4(TNC):c.5613A>G (p.Lys1871=)	LOC126860740, TNC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1317669	NM_002160.4(TNC):c.5531C>T (p.Thr1844Met)	LOC126860740, TNC (T1844M)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1316827	NM_002160.4(TNC):c.5513-105C>T	LOC126860740, TNC	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1317842	NM_002160.4(TNC):c.5513-291A>T	LOC126860740, TNC	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1267151	NM_002160.4(TNC):c.5513-312C>G	LOC126860740, TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227716	NM_002160.4(TNC):c.5513-317G>A	LOC126860740, TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274867	NM_002160.4(TNC):c.5512+123A>T	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317130	NM_002160.4(TNC):c.5512+68G>A	TNC	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1224906	NM_002160.4(TNC):c.5393-35A>G	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268788	NM_002160.4(TNC):c.5392+235C>A	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316251	NM_002160.4(TNC):c.5392+17GT[12]	TNC	Microsatellite (intron variant)	not provided	GLikely benign
Select item 1263418	NM_002160.4(TNC):c.5392+17GT[10]	TNC	Microsatellite (intron variant)	not provided	GBenign
Select item 1240676	NM_002160.4(TNC):c.5392+17GT[11]	TNC	Microsatellite (intron variant)	not provided	GBenign
Select item 1318115	NM_002160.4(TNC):c.5392+17GT[8]	TNC	Microsatellite (intron variant)	not provided	GLikely benign
Select item 586835	NM_002160.4(TNC):c.5341G>A (p.Ala1781Thr)	TNC (A1781T)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 56 +1 more	GBenign
Select item 1289528	NM_002160.4(TNC):c.5249-17C>G	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279260	NM_002160.4(TNC):c.5249-217del	TNC	Deletion (intron variant)	not provided	GBenign
Select item 1248638	NM_002160.4(TNC):c.5249-218_5249-217del	TNC	Deletion (intron variant)	not provided	GBenign
Select item 1233778	NM_002160.4(TNC):c.5249-220_5249-217del	TNC	Deletion (intron variant)	not provided	GBenign
Select item 1229498	NM_002160.4(TNC):c.5249-217T>C	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286406	NM_002160.4(TNC):c.5249-220T>C	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245493	NM_002160.4(TNC):c.5249-220del	TNC	Deletion (intron variant)	not provided	GBenign
Select item 1223127	NM_002160.4(TNC):c.5249-220T>G	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230486	NM_002160.4(TNC):c.5249-224_5249-223insG	TNC	Insertion (intron variant)	not provided	GBenign
Select item 1286132	NM_002160.4(TNC):c.5249-225G>C	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1256687	NM_002160.4(TNC):c.5249-225del	TNC	Deletion (intron variant)	not provided	GBenign
Select item 1241469	NM_002160.4(TNC):c.5249-227C>G	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317670	NM_002160.4(TNC):c.5249-231_5249-229del	TNC	Deletion (intron variant)	not provided	GLikely benign
Select item 1251156	NM_002160.4(TNC):c.5249-230C>T	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260935	NM_002160.4(TNC):c.5249-231T>C	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316953	NM_002160.4(TNC):c.5249-248G>A	TNC	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1237439	NM_002160.4(TNC):c.5248+98T>G	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 721116	NM_002160.4(TNC):c.5223G>A (p.Arg1741=)	TNC	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 56 +1 more	GBenign/Likely benign
Select item 1222923	NM_002160.4(TNC):c.5202A>G (p.Thr1734=)	TNC	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 776445	NM_002160.4(TNC):c.5193G>A (p.Arg1731=)	TNC	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1274158	NM_002160.4(TNC):c.5126-47A>G	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260925	NM_002160.4(TNC):c.5126-329A>C	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282803	NM_002160.4(TNC):c.5125+201G>A	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 773511	NM_002160.4(TNC):c.5093G>A (p.Arg1698Gln)	TNC (R1698Q)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 56 +1 more	GBenign
Select item 724494	NM_002160.4(TNC):c.5093G>C (p.Arg1698Pro)	TNC (R1698P)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 56 +1 more	GBenign/Likely benign
Select item 1238979	NM_002160.4(TNC):c.5029A>T (p.Ile1677Leu)	TNC (I1677L)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 56 +1 more	GBenign
Select item 1315760	NM_002160.4(TNC):c.4944C>T (p.Asp1648=)	TNC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1222890	NM_002160.4(TNC):c.4852+298T>A	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251814	NM_002160.4(TNC):c.4852+289C>A	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295633	NM_002160.4(TNC):c.4852+244C>T	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 782147	NM_002160.4(TNC):c.4740C>T (p.Thr1580=)	TNC	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 56 +1 more	GBenign
Select item 1316826	NM_002160.4(TNC):c.4580-198C>T	TNC	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1253601	NM_002160.4(TNC):c.4579+43T>A	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244857	NM_002160.4(TNC):c.4575G>A (p.Thr1525=)	TNC	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 56 +1 more	GBenign
Select item 1227583	NM_002160.4(TNC):c.4543A>G (p.Ile1515Val)	TNC (I1515V)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1315683	NM_002160.4(TNC):c.4481A>G (p.His1494Arg)	TNC (H1494R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1318423	NM_002160.4(TNC):c.4472G>A (p.Arg1491Gln)	TNC (R1491Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1276293	NM_002160.4(TNC):c.4307-48_4307-45del	TNC	Deletion (intron variant)	not provided	GBenign
Select item 1232370	NM_002160.4(TNC):c.4306+263T>G	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283677	NM_002160.4(TNC):c.4306+119C>T	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1328900	NM_002160.4(TNC):c.4233G>A (p.Thr1411=)	TNC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1230265	NM_002160.4(TNC):c.4182G>A (p.Thr1394=)	TNC	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1318370	NM_002160.4(TNC):c.4104C>T (p.Thr1368=)	TNC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1239331	NM_002160.4(TNC):c.4034-71G>A	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316684	NM_002160.4(TNC):c.4034-104dup	TNC	Duplication (intron variant)	not provided	GLikely benign
Select item 1228815	NM_002160.4(TNC):c.4033+308del	TNC	Deletion (intron variant)	not provided	GBenign
Select item 1316669	NM_002160.4(TNC):c.4033+265A>G	TNC	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1317976	NM_002160.4(TNC):c.4033+243GT[5]	TNC	Microsatellite (intron variant)	not provided	GLikely benign
Select item 1276921	NM_002160.4(TNC):c.4033+111C>T	TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317409	NM_002160.4(TNC):c.4011C>G (p.Pro1337=)	TNC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1320566	NM_002160.4(TNC):c.3909G>A (p.Thr1303=)	TNC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1318164	NM_002160.4(TNC):c.3834G>A (p.Thr1278=)	TNC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1183557	NM_002160.4(TNC):c.3761-136C>T	LOC126860741, TNC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274023	NM_002160.4(TNC):c.3760+129G>A	LOC126860741, TNC	Single nucleotide variant (intron variant)	not provided	GBenign

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