"Ambry Genetics"[submitter] AND "PRSS21"[gene] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2219022	NM_006799.4(PRSS21):c.7G>A (p.Ala3Thr)	LOC130058270, PRSS21 (A3T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3219820	NM_006799.4(PRSS21):c.47C>G (p.Ala16Gly)	LOC130058270, PRSS21 (A16G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2617881	NM_006799.4(PRSS21):c.199T>C (p.Cys67Arg)	PRSS21 (C67R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379823	NM_006799.4(PRSS21):c.235A>T (p.Thr79Ser)	PRSS21 (T79S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3219818	NM_006799.4(PRSS21):c.236C>T (p.Thr79Met)	PRSS21 (T79M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482215	NM_006799.4(PRSS21):c.247T>A (p.Cys83Ser)	PRSS21 (C83S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254535	NM_006799.4(PRSS21):c.254A>C (p.Glu85Ala)	PRSS21 (E85A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2310410	NM_006799.4(PRSS21):c.341C>A (p.Ala114Asp)	PRSS21 (A112D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310670	NM_006799.4(PRSS21):c.373T>C (p.Tyr125His)	PRSS21 (Y123H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2255980	NM_006799.4(PRSS21):c.386G>A (p.Arg129His)	PRSS21 (R129H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2306250	NM_006799.4(PRSS21):c.421G>T (p.Val141Leu)	PRSS21 (V139L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2591759	NM_006799.4(PRSS21):c.426G>C (p.Lys142Asn)	PRSS21 (K140N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591994	NM_006799.4(PRSS21):c.433G>C (p.Ala145Pro)	PRSS21 (A145P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473487	NM_006799.4(PRSS21):c.448A>G (p.Thr150Ala)	PRSS21 (T150A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469618	NM_006799.4(PRSS21):c.464C>T (p.Pro155Leu)	PRSS21 (P153L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3219821	NM_006799.4(PRSS21):c.503G>A (p.Arg168Gln)	PRSS21 (R166Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3219822	NM_006799.4(PRSS21):c.607A>G (p.Met203Val)	PRSS21 (M201V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3219823	NM_006799.4(PRSS21):c.680C>T (p.Ala227Val)	PRSS21 (A227V +1 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 2265037	NM_006799.4(PRSS21):c.698C>G (p.Ala233Gly)	PRSS21 (A231G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235462	NM_006799.4(PRSS21):c.884C>T (p.Pro295Leu)	PRSS21 (P295L +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3219825	NM_006799.4(PRSS21):c.893C>T (p.Pro298Leu)	PRSS21 (P296L +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GLikely benign
Select item 3219826	NM_006799.4(PRSS21):c.898C>T (p.Leu300Phe)	PRSS21 (L286F +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2377753	NM_006799.4(PRSS21):c.925C>G (p.Pro309Ala)	PRSS21 (P309A +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance

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Items: 23