ClinVar (all) for Orgtrack (Select 505298) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 161990	NM_002769.5(PRSS1):c.390C>T (p.Thr130=)	PRSS1, TRB	Single nucleotide variant (synonymous variant)	Hereditary pancreatitis +2 more	GBenign/Likely benign
Select item 161989	NM_002769.5(PRSS1):c.360C>T (p.Asn120=)	PRSS1, TRB	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 161988	NM_002769.5(PRSS1):c.354A>C (p.Val118=)	PRSS1, TRB	Single nucleotide variant (synonymous variant)	Hereditary pancreatitis	GLikely benign
Select item 161987	NM_002769.5(PRSS1):c.351A>C (p.Ala117=)	PRSS1, TRB	Single nucleotide variant (synonymous variant)	Hereditary pancreatitis	GLikely benign
Select item 161986	NM_002769.5(PRSS1):c.347G>C (p.Arg116Pro)	PRSS1, TRB (R116P)	Single nucleotide variant (missense variant)	Hereditary pancreatitis	GLikely pathogenic
Select item 161985	NM_002769.5(PRSS1):c.343T>A (p.Ser115Thr)	PRSS1, TRB (S115T)	Single nucleotide variant (missense variant)	Hereditary pancreatitis	GLikely benign
Select item 11882	NM_002769.5(PRSS1):c.365_366delinsAT (p.Arg122His)	PRSS1, TRB (R122H)	Indel (missense variant)	Hereditary pancreatitis	GPathogenic

ClinVar