"Ambry Genetics"[submitter] AND "YPEL4"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2468348	NM_145008.3(YPEL4):c.242C>T (p.Ser81Leu)	MIR130AHG, YPEL4 (S81L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191628	NM_145008.3(YPEL4):c.196G>A (p.Gly66Ser)	MIR130AHG, YPEL4 (G66S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191629	NM_145008.3(YPEL4):c.97C>T (p.His33Tyr)	MIR130AHG, YPEL4 (H33Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601109	NM_145008.3(YPEL4):c.70C>T (p.Arg24Cys)	MIR130AHG, YPEL4 (R24C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281367	NM_145008.3(YPEL4):c.19G>A (p.Gly7Ser)	MIR130AHG, YPEL4 (G7S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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