Related gene-specific medical variations for Gene (Select 10750) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3051338	NM_006613.4(GRAP):c.546C>T (p.Gly182=)	GRAP, SLC5A10 (A126V)	Single nucleotide variant (missense variant +2 more)	GRAP-related disorder	GLikely benign
Select item 3043072	NM_006613.4(GRAP):c.603C>T (p.Cys201=)	GRAP, SLC5A10 (A145V)	Single nucleotide variant (missense variant +2 more)	GRAP-related disorder	GLikely benign
Select item 3036303	NM_006613.4(GRAP):c.595C>A (p.Arg199=)	GRAP, SLC5A10	Single nucleotide variant (synonymous variant +1 more)	GRAP-related disorder	GLikely benign
Select item 2519138	NM_006613.4(GRAP):c.590G>A (p.Arg197Gln)	GRAP, SLC5A10 (R197Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226091	NM_006613.4(GRAP):c.479C>T (p.Ala160Val)	GRAP, SLC5A10 (A160V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220557	NM_006613.4(GRAP):c.533G>C (p.Ser178Thr)	GRAP, SLC5A10 (A122P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar