Related gene-specific medical variations for Gene (Select 9726) - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2484223	NM_001039503.3(PRSS53):c.1618C>T (p.Pro540Ser)	PRSS53, ZNF646 (P540S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2303609	NM_001039503.3(PRSS53):c.1588T>C (p.Phe530Leu)	PRSS53, ZNF646 (F530L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2207395	NM_001039503.3(PRSS53):c.1594G>A (p.Glu532Lys)	PRSS53, ZNF646 (E532K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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