NME3[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3352216	NM_002513.3(NME3):c.477G>A (p.Trp159Ter)	NME3 (W159*)	Single nucleotide variant (nonsense)	NME3-related condition	GLikely benign
Select item 2208206	NM_002513.3(NME3):c.469C>T (p.Leu157Phe)	NME3 (L157F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266100	NM_002513.3(NME3):c.434G>A (p.Arg145His)	NME3 (R145H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1301639	NM_002513.3(NME3):c.177+15_177+33del	NME3	Deletion (intron variant)	not specified	GLikely benign

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