"Ambry Genetics"[submitter] AND "SPRYD7"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2605277	NM_020456.4(SPRYD7):c.550C>T (p.Pro184Ser)	SPRYD7 (P145S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2606266	NM_020456.4(SPRYD7):c.467G>A (p.Arg156Gln)	SPRYD7 (R117Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364776	NM_020456.4(SPRYD7):c.463A>G (p.Ile155Val)	SPRYD7 (I116V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524459	NM_020456.4(SPRYD7):c.392G>T (p.Gly131Val)	SPRYD7 (G92V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3169430	NM_020456.4(SPRYD7):c.323T>C (p.Leu108Pro)	SPRYD7 (L69P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3322388	NM_020456.4(SPRYD7):c.226A>G (p.Ile76Val)	SPRYD7 (I37V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217216	NM_020456.4(SPRYD7):c.107G>A (p.Gly36Glu)	SPRYD7 (G36E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3169431	NM_020456.4(SPRYD7):c.32G>A (p.Cys11Tyr)	LOC130009785, SPRYD7 (C11Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar