Related gene-specific medical variations for Gene (Select 130059492) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3326965	NM_015251.3(ATMIN):c.67C>T (p.Pro23Ser)	LOC130059492, ATMIN (P23S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131098	NM_015251.3(ATMIN):c.47C>T (p.Ala16Val)	ATMIN, LOC130059492 (A16V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482853	NM_015251.3(ATMIN):c.29C>A (p.Ala10Glu)	ATMIN, LOC130059492 (A10E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400337	NM_015251.3(ATMIN):c.56C>G (p.Ala19Gly)	ATMIN, LOC130059492 (A19G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367766	NM_015251.3(ATMIN):c.71C>T (p.Ala24Val)	ATMIN, LOC130059492 (A24V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2321423	NM_015251.3(ATMIN):c.26C>T (p.Ala9Val)	ATMIN, LOC130059492 (A9V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319235	NM_015251.3(ATMIN):c.68C>T (p.Pro23Leu)	ATMIN, LOC130059492 (P23L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205232	NM_015251.3(ATMIN):c.8C>G (p.Ala3Gly)	ATMIN, LOC130059492 (A3G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar