"WangQJ Lab, Chinese People's Liberation Army General Hospital"[submit - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1185102	NM_001145026.2(PTPRQ):c.3873+5G>T	PTPRQ	Single nucleotide variant (intron variant)	Autosomal recessive nonsyndromic hearing loss 84A	GUncertain significance
Select item 1185120	NM_001145026.2(PTPRQ):c.6113C>T (p.Pro2038Leu)	PTPRQ (P2038L)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 84A	GUncertain significance
Select item 1185053	NM_001145026.2(PTPRQ):c.6194_6453+1del	PTPRQ	Deletion (splice acceptor variant +1 more)	Autosomal recessive nonsyndromic hearing loss 84A	GLikely pathogenic
Select item 1185114	NM_001145026.2(PTPRQ):c.6526G>A (p.Ala2176Thr)	PTPRQ (A2176T)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1185103	NM_001145026.2(PTPRQ):c.6602G>A (p.Ser2201Asn)	PTPRQ (S2201N)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 84A	GUncertain significance
Select item 1185134	NM_001145026.2(PTPRQ):c.6603-3T>G	PTPRQ	Single nucleotide variant (intron variant)	not provided	GUncertain significance

ClinVar