GYPE[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3283207	NM_198682.3(GYPE):c.193G>C (p.Val65Leu)	GYPE (V65L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103380	NM_198682.3(GYPE):c.170G>A (p.Arg57His)	GYPE (R57H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514572	NM_198682.3(GYPE):c.169C>G (p.Arg57Gly)	GYPE (R57G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385324	NM_198682.3(GYPE):c.169C>T (p.Arg57Cys)	GYPE (R57C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545085	NM_198682.3(GYPE):c.149T>C (p.Ile50Thr)	GYPE (I50T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516123	NM_198682.3(GYPE):c.141A>G (p.Ile47Met)	GYPE (I47M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 402918	NM_198682.3(GYPE):c.38G>C (p.Gly13Ala)	GYPE (G13A)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 769294	NM_198682.3(GYPE):c.38-9T>G	GYPE	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar