Related gene-specific medical variations for Gene (Select 79707) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3300289	NM_024654.5(NOL9):c.245C>A (p.Thr82Asn)	LOC129929248, NOL9 (T82N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460310	NM_024654.5(NOL9):c.199C>A (p.Arg67Ser)	LOC129929248, NOL9 (R67S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355717	NM_024654.5(NOL9):c.61C>A (p.Arg21Ser)	LOC129929248, NOL9 (R21S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352852	NM_024654.5(NOL9):c.29G>A (p.Arg10Gln)	LOC129929248, NOL9 (R10Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283979	NM_024654.5(NOL9):c.188G>A (p.Arg63Lys)	LOC129929248, NOL9 (R63K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283300	NM_024654.5(NOL9):c.233C>G (p.Pro78Arg)	LOC129929248, NOL9 (P78R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257600	NM_024654.5(NOL9):c.241G>T (p.Ala81Ser)	LOC129929248, NOL9 (A81S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210840	NM_024654.5(NOL9):c.218C>T (p.Ala73Val)	LOC129929248, NOL9 (A73V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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