C2750082[trait identifier] AND "ARUP Laboratories, Molecular Genetics - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 440352	NM_001128228.3(TPRN):c.1936G>A (p.Glu646Lys)	TPRN (E646K)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 165579	NM_001128228.3(TPRN):c.1818GGA[8] (p.Glu621del)	TPRN (E621del)	Microsatellite (inframe_deletion)	not specified +2 more	GBenign
Select item 1199833	NM_001128228.3(TPRN):c.1725+5G>A	TPRN	Single nucleotide variant (intron variant)	Autosomal recessive nonsyndromic hearing loss 79 +1 more	GUncertain significance
Select item 811203	NM_001128228.3(TPRN):c.1696C>T (p.Leu566Phe)	TPRN (L566F)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 513463	NM_001128228.3(TPRN):c.1073T>C (p.Leu358Pro)	TPRN (L358P)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 79 +2 more	GBenign
Select item 193179	NM_001128228.3(TPRN):c.858C>T (p.Cys286=)	TPRN	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 193181	NM_001128228.3(TPRN):c.559G>T (p.Ala187Ser)	TPRN (A187S)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 79 +2 more	GBenign

ClinVar