"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "FBXO38"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1693902	NM_205836.3(FBXO38):c.157A>G (p.Met53Val)	FBXO38 (M53V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 473955	NM_205836.3(FBXO38):c.239G>A (p.Arg80Gln)	FBXO38 (R80Q)	Single nucleotide variant (missense variant)	Distal hereditary motor neuropathy type 2 +1 more	GUncertain significance
Select item 3379605	NM_205836.3(FBXO38):c.770G>C (p.Gly257Ala)	FBXO38 (G257A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1001987	NM_205836.3(FBXO38):c.812G>A (p.Arg271Gln)	FBXO38 (R271Q)	Single nucleotide variant (missense variant)	Distal hereditary motor neuropathy type 2 +1 more	GUncertain significance
Select item 3379606	NM_205836.3(FBXO38):c.1061A>T (p.His354Leu)	FBXO38 (H354L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1693903	NM_205836.3(FBXO38):c.3137G>A (p.Arg1046His)	FBXO38 (R1046H +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

ClinVar