"Ambry Genetics"[submitter] AND "PRSS36"[gene] - ClinVar

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Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2459777	NM_173502.5(PRSS36):c.2468C>G (p.Thr823Ser)	PRSS36 (T823S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2406553	NM_173502.5(PRSS36):c.2464C>T (p.Pro822Ser)	PRSS36 (P719S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2561160	NM_173502.5(PRSS36):c.2369G>C (p.Arg790Pro)	PRSS36 (R785P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2548206	NM_173502.5(PRSS36):c.2344G>C (p.Val782Leu)	PRSS36 (V777L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2230148	NM_173502.5(PRSS36):c.2344G>A (p.Val782Met)	PRSS36 (V679M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2514936	NM_173502.5(PRSS36):c.2333C>A (p.Ser778Tyr)	PRSS36 (S778Y +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2374531	NM_173502.5(PRSS36):c.2324C>T (p.Thr775Met)	PRSS36 (T775M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2603326	NM_173502.5(PRSS36):c.2264C>G (p.Ala755Gly)	PRSS36 (A755G +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2330600	NM_173502.5(PRSS36):c.2125G>T (p.Ala709Ser)	PRSS36 (A704S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2412244	NM_173502.5(PRSS36):c.2063G>A (p.Arg688Gln)	PRSS36 (R683Q +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2257949	NM_173502.5(PRSS36):c.2062C>T (p.Arg688Trp)	PRSS36 (R683W +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2260933	NM_173502.5(PRSS36):c.2033C>T (p.Pro678Leu)	PRSS36 (P678L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2267698	NM_173502.5(PRSS36):c.1988G>A (p.Arg663His)	PRSS36 (R658H +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2284199	NM_173502.5(PRSS36):c.1979A>T (p.Gln660Leu)	PRSS36 (Q655L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2548140	NM_173502.5(PRSS36):c.1969C>G (p.Gln657Glu)	PRSS36 (Q657E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2607250	NM_173502.5(PRSS36):c.1961C>T (p.Ser654Phe)	PRSS36 (S654F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2398795	NM_173502.5(PRSS36):c.1958G>C (p.Ser653Thr)	PRSS36 (S648T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2619816	NM_173502.5(PRSS36):c.1741C>G (p.Pro581Ala)	PRSS36 (P576A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2295410	NM_173502.5(PRSS36):c.1703G>A (p.Gly568Asp)	PRSS36 (G563D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2238384	NM_173502.5(PRSS36):c.1516T>G (p.Cys506Gly)	LOC130058894, PRSS36 (C506G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2207943	NM_173502.5(PRSS36):c.1506G>C (p.Glu502Asp)	LOC130058894, PRSS36 (E502D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2396505	NM_173502.5(PRSS36):c.1450C>T (p.Pro484Ser)	LOC130058894, PRSS36 (P484S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2330463	NM_173502.5(PRSS36):c.1424T>A (p.Leu475Gln)	LOC130058894, PRSS36 (L475Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2347856	NM_173502.5(PRSS36):c.1403G>A (p.Gly468Asp)	LOC130058894, PRSS36 (G468D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2401681	NM_173502.5(PRSS36):c.1321G>A (p.Gly441Arg)	LOC130058894, PRSS36 (G441R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2313604	NM_173502.5(PRSS36):c.1271C>G (p.Ala424Gly)	LOC130058894, PRSS36 (A424G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2205001	NM_173502.5(PRSS36):c.761G>A (p.Arg254His)	PRSS36 (R254H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2264818	NM_173502.5(PRSS36):c.655A>G (p.Thr219Ala)	PRSS36 (T219A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2507664	NM_173502.5(PRSS36):c.640G>A (p.Gly214Ser)	PRSS36 (G214S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2248513	NM_173502.5(PRSS36):c.220G>A (p.Gly74Ser)	PRSS36 (G74S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2301379	NM_173502.5(PRSS36):c.176C>T (p.Pro59Leu)	PRSS36 (P59L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2548720	NM_173502.5(PRSS36):c.170C>A (p.Thr57Asn)	PRSS36 (T57N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2597147	NM_173502.5(PRSS36):c.118C>T (p.Arg40Cys)	PRSS36 (R40C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2465331	NM_173502.5(PRSS36):c.59C>A (p.Ala20Asp)	PRSS36 (A20D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2523351	NM_173502.5(PRSS36):c.33G>C (p.Met11Ile)	PRSS36 (M11I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2467517	NM_173502.5(PRSS36):c.33G>A (p.Met11Ile)	PRSS36 (M11I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2618400	NM_173502.5(PRSS36):c.32T>C (p.Met11Thr)	PRSS36 (M11T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 37