"Genome-Nilou Lab"[submitter] AND "ARSG"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1166453	NM_001267727.2(ARSG):c.707C>G (p.Thr236Ser)	ARSG (T220S +1 more)	Single nucleotide variant (missense variant +1 more)	Usher syndrome, type 4 +1 more	GBenign
Select item 1165514	NM_001267727.2(ARSG):c.765T>C (p.Pro255=)	ARSG	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1166454	NM_001267727.2(ARSG):c.820T>C (p.Trp274Arg)	ARSG (W258R +2 more)	Single nucleotide variant (missense variant)	Usher syndrome, type 4 +1 more	GBenign

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