C1853276[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1034398	NM_001039141.3(TRIOBP):c.964G>T (p.Ala322Ser)	TRIOBP (A322S)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 28 +1 more	GConflicting classifications of pathogenicity
Select item 1034393	NM_001039141.3(TRIOBP):c.1195C>G (p.Arg399Gly)	TRIOBP (R399G)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 28	GUncertain significance
Select item 1034394	NM_001039141.3(TRIOBP):c.3214C>G (p.Arg1072Gly)	TRIOBP (R1072G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1034396	NM_001039141.3(TRIOBP):c.4483G>T (p.Glu1495Ter)	TRIOBP (E1495*)	Single nucleotide variant (nonsense)	Autosomal recessive nonsyndromic hearing loss 28	GUncertain significance
Select item 504691	NM_001039141.3(TRIOBP):c.5014G>T (p.Gly1672Ter)	TRIOBP (G1672*)	Single nucleotide variant (nonsense)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 1034397	NM_001039141.3(TRIOBP):c.6632A>T (p.Gln2211Leu)	TRIOBP (Q498L +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance

ClinVar