Related gene-specific medical variations for Gene (Select 3613) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3285972	NM_014214.3(IMPA2):c.40G>T (p.Gly14Cys)	IMPA2, LOC125368548 (G14C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109563	NM_014214.3(IMPA2):c.76C>G (p.Leu26Val)	IMPA2, LOC125368548 (L26V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523631	NM_014214.3(IMPA2):c.8C>T (p.Pro3Leu)	IMPA2, LOC125368548 (P3L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373170	NM_014214.3(IMPA2):c.85C>G (p.Arg29Gly)	IMPA2, LOC125368548 (R29G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373168	NM_014214.3(IMPA2):c.83T>G (p.Leu28Arg)	IMPA2, LOC125368548 (L28R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373167	NM_014214.3(IMPA2):c.82C>G (p.Leu28Val)	IMPA2, LOC125368548 (L28V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373166	NM_014214.3(IMPA2):c.80C>G (p.Ala27Gly)	IMPA2, LOC125368548 (A27G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373165	NM_014214.3(IMPA2):c.73C>G (p.Gln25Glu)	IMPA2, LOC125368548 (Q25E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361351	NM_014214.3(IMPA2):c.29C>T (p.Ala10Val)	IMPA2, LOC125368548 (A10V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355514	NM_014214.3(IMPA2):c.65C>A (p.Ala22Glu)	IMPA2, LOC125368548 (A22E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance