"Fulgent Genetics, Fulgent Genetics"[submitter] AND "SASH1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1290003	NM_015278.5(SASH1):c.45CGAGCC[3] (p.12EP[7])	SASH1	Microsatellite (5 prime UTR variant +2 more)	not provided +2 more	GBenign
Select item 789886	NM_015278.5(SASH1):c.2459G>A (p.Arg820Gln)	SASH1 (R703Q +5 more)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 783757	NM_015278.5(SASH1):c.3266G>A (p.Arg1089Gln)	SASH1 (R1044Q +5 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign

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