"Baylor Genetics"[submitter] AND "TNC"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2441982	NM_002160.4(TNC):c.4490G>C (p.Gly1497Ala)	TNC (G1406A +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 56	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 444776	NM_002160.4(TNC):c.2960C>T (p.Thr987Met)	TNC (T987M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1033486	NM_002160.4(TNC):c.2795G>C (p.Gly932Ala)	TNC (G932A)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 56	GUncertain significance
Select item 1029565	NM_002160.4(TNC):c.2239C>T (p.Arg747Trp)	TNC (R747W)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 56 +1 more	GUncertain significance
Select item 1029564	NM_002160.4(TNC):c.1580G>C (p.Cys527Ser)	TNC (C527S)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 56	GUncertain significance

ClinVar