"PreventionGenetics, part of Exact Sciences"[submitter] AND "TRB"[gene - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2632422	NM_002769.5(PRSS1):c.2T>G (p.Met1Arg)	PRSS1, TRB (M1R)	Single nucleotide variant (missense variant +2 more)	Hereditary pancreatitis +1 more	GUncertain significance
Select item 258798	NM_002769.5(PRSS1):c.200+8T>C	PRSS1, TRB	Single nucleotide variant (intron variant)	Hereditary pancreatitis +1 more	GLikely benign
Select item 11876	NM_002769.5(PRSS1):c.365G>A (p.Arg122His)	PRSS1, TRB (R122H)	Single nucleotide variant (missense variant)	Hereditary pancreatitis +2 more	GPathogenic
Select item 258799	NM_002769.5(PRSS1):c.444G>A (p.Ala148=)	PRSS1, TRB	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 239391	NM_002769.5(PRSS1):c.486T>C (p.Asp162=)	PRSS1, TRB	Single nucleotide variant (synonymous variant)	Hereditary pancreatitis +1 more	GBenign/Likely benign
Select item 258800	NM_002769.5(PRSS1):c.592-11C>T	PRSS1, TRB	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 258801	NM_002769.5(PRSS1):c.592-9T>C	PRSS1, TRB	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 258802	NM_002769.5(PRSS1):c.623G>C (p.Gly208Ala)	PRSS1, TRB (G208A)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 258803	NM_002769.5(PRSS1):c.738T>C (p.Asn246=)	PRSS1, TRB	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign