Related gene-specific medical variations for Gene (Select 29997) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3300370	NM_015710.5(NOP53):c.172C>G (p.Leu58Val)	LOC130064829, NOP53 (L58V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300369	NM_015710.5(NOP53):c.167T>C (p.Leu56Pro)	LOC130064829, NOP53 (L56P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3201239	NM_015710.5(NOP53):c.33G>T (p.Lys11Asn)	LOC130064829, NOP53 (K11N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3201228	NM_015710.5(NOP53):c.116G>C (p.Arg39Pro)	LOC130064829, NOP53 (R39P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2624106	NM_015710.5(NOP53):c.132G>C (p.Lys44Asn)	LOC130064829, NOP53 (K44N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588965	NM_015710.5(NOP53):c.187T>C (p.Phe63Leu)	LOC130064829, NOP53 (F63L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547040	NM_015710.5(NOP53):c.7G>A (p.Ala3Thr)	LOC130064829, NOP53 (A3T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541140	NM_015710.5(NOP53):c.5C>T (p.Ala2Val)	LOC130064829, NOP53 (A2V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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