Related gene-specific medical variations for Gene (Select 56902) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2268716	NM_020143.4(PNO1):c.191G>A (p.Cys64Tyr)	LOC129933975, PNO1 (C64Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262807	NM_020143.4(PNO1):c.172C>G (p.Pro58Ala)	LOC129933975, PNO1 (P58A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254329	NM_020143.4(PNO1):c.173C>T (p.Pro58Leu)	LOC129933975, PNO1 (P58L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234479	NM_020143.4(PNO1):c.185C>T (p.Pro62Leu)	LOC129933975, PNO1 (P62L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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