"King Laboratory, University of Washington"[submitter] AND "MYO15A"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2445655	NM_016239.4(MYO15A):c.6194del (p.Met2065fs)	MYO15A (M2065fs)	Deletion (frameshift variant)	Autosomal recessive nonsyndromic hearing loss 3	GPathogenic
Select item 2445656	NM_016239.4(MYO15A):c.6599C>A (p.Ser2200Ter)	MYO15A (S2200*)	Single nucleotide variant (nonsense)	Autosomal recessive nonsyndromic hearing loss 3	GPathogenic
Select item 1476534	NM_016239.4(MYO15A):c.8080C>A (p.Arg2694Ser)	MYO15A (R2694S)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2445657	NM_016239.4(MYO15A):c.8831del (p.Pro2944fs)	MYO15A (P2944fs)	Deletion (frameshift variant)	Autosomal recessive nonsyndromic hearing loss 3	GPathogenic
Select item 2445658	NM_016239.4(MYO15A):c.9443G>A (p.Cys3148Tyr)	MYO15A (C3148Y)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GLikely pathogenic
Select item 2445659	NM_016239.4(MYO15A):c.10351-15T>G	MYO15A	Single nucleotide variant (intron variant)	Autosomal recessive nonsyndromic hearing loss 3 +1 more	GConflicting classifications of pathogenicity

ClinVar