"Clinical Genetics, Academic Medical Center"[submitter] AND "USH1C"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 178565	NM_153676.4(USH1C):c.2184+10T>C	USH1C	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 1284325	NM_153676.4(USH1C):c.1596C>T (p.Phe532=)	USH1C	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 303804	NM_005709.4(USH1C):c.1220G>A (p.Gly407Glu)	USH1C (G407E +1 more)	Single nucleotide variant (missense variant +1 more)	Usher syndrome type 1C +1 more	GConflicting classifications of pathogenicity
Select item 47975	NM_153676.4(USH1C):c.1136G>A (p.Gly379Asp)	USH1C (G379D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 178643	NM_153676.4(USH1C):c.946G>C (p.Glu316Gln)	USH1C (E316Q +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 48014	NM_153676.4(USH1C):c.381G>T (p.Gly127=)	USH1C	Single nucleotide variant (synonymous variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity

ClinVar