"Ambry Genetics"[submitter] AND "PRSS55"[gene] - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2482641	NM_198464.4(PRSS55):c.61C>T (p.Arg21Trp)	PRSS51, PRSS55 (R21W)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2468032	NM_198464.4(PRSS55):c.76G>A (p.Glu26Lys)	PRSS51, PRSS55 (E26K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274900	NM_198464.4(PRSS55):c.103G>A (p.Ala35Thr)	PRSS51, PRSS55 (A35T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338312	NM_198464.4(PRSS55):c.127C>A (p.Pro43Thr)	PRSS51, PRSS55 (P43T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3219921	NM_198464.4(PRSS55):c.143G>T (p.Ser48Ile)	PRSS51, PRSS55 (S48I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533230	NM_198464.4(PRSS55):c.157T>C (p.Cys53Arg)	PRSS51, PRSS55 (C53R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349841	NM_198464.4(PRSS55):c.172A>G (p.Ile58Val)	PRSS51, PRSS55 (I58V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392686	NM_198464.4(PRSS55):c.190C>T (p.Arg64Trp)	PRSS51, PRSS55 (R64W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219922	NM_198464.4(PRSS55):c.206C>T (p.Thr69Ile)	PRSS51, PRSS55 (T69I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2269931	NM_198464.4(PRSS55):c.258G>C (p.Gln86His)	PRSS51, PRSS55 (Q86H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602735	NM_198464.4(PRSS55):c.306G>C (p.Trp102Cys)	PRSS51, PRSS55 (W102C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219923	NM_198464.4(PRSS55):c.310C>G (p.Leu104Val)	PRSS51, PRSS55 (L104V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2462049	NM_198464.4(PRSS55):c.317C>T (p.Ala106Val)	PRSS51, PRSS55 (A106V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219924	NM_198464.4(PRSS55):c.343C>G (p.Leu115Val)	PRSS51, PRSS55 (L115V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588139	NM_198464.4(PRSS55):c.367G>A (p.Val123Met)	PRSS55, PRSS51 (V123M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611292	NM_198464.4(PRSS55):c.381C>T (p.Asn127=)	PRSS51, PRSS55	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2563094	NM_198464.4(PRSS55):c.382G>A (p.Asp128Asn)	PRSS51, PRSS55 (D128N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228022	NM_198464.4(PRSS55):c.407T>C (p.Ile136Thr)	PRSS51, PRSS55 (I136T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394781	NM_198464.4(PRSS55):c.439G>A (p.Asp147Asn)	PRSS51, PRSS55 (D147N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310730	NM_198464.4(PRSS55):c.446A>G (p.Lys149Arg)	PRSS51, PRSS55 (K149R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376909	NM_198464.4(PRSS55):c.466G>A (p.Asp156Asn)	PRSS51, PRSS55 (D156N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310734	NM_198464.4(PRSS55):c.536C>T (p.Thr179Met)	PRSS51, PRSS55 (T179M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359708	NM_198464.4(PRSS55):c.536C>G (p.Thr179Arg)	PRSS51, PRSS55 (T179R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2591141	NM_198464.4(PRSS55):c.556T>C (p.Trp186Arg)	PRSS51, PRSS55 (W186R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219925	NM_198464.4(PRSS55):c.560G>A (p.Arg187His)	PRSS51, PRSS55 (R187H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3219926	NM_198464.4(PRSS55):c.640A>G (p.Met214Val)	PRSS51, PRSS55 (M214V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219928	NM_198464.4(PRSS55):c.650T>C (p.Met217Thr)	PRSS51, PRSS55 (M217T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219927	NM_198464.4(PRSS55):c.650T>A (p.Met217Lys)	PRSS51, PRSS55 (M217K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281884	NM_198464.4(PRSS55):c.663G>C (p.Glu221Asp)	PRSS51, PRSS55 (E221D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306134	NM_198464.4(PRSS55):c.675G>T (p.Met225Ile)	PRSS51, PRSS55 (M225I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310731	NM_198464.4(PRSS55):c.704G>C (p.Cys235Ser)	PRSS51, PRSS55 (C235S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614568	NM_198464.4(PRSS55):c.770C>T (p.Thr257Ile)	PRSS51, PRSS55 (T257I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608053	NM_198464.4(PRSS55):c.860C>T (p.Ser287Leu)	PRSS51, PRSS55 (S287L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2599257	NM_198464.4(PRSS55):c.885C>G (p.Ile295Met)	PRSS51, PRSS55 (I295M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507729	NM_198464.4(PRSS55):c.902T>C (p.Leu301Pro)	PRSS51, PRSS55 (L301P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310732	NM_198464.4(PRSS55):c.917T>G (p.Phe306Cys)	PRSS51, PRSS55 (F306C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3219929	NM_198464.4(PRSS55):c.974C>T (p.Ser325Leu)	PRSS51, PRSS55 (S325L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342961	NM_198464.4(PRSS55):c.982C>T (p.Pro328Ser)	PRSS51, PRSS55 (P328S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314985	NM_198464.4(PRSS55):c.982C>G (p.Pro328Ala)	PRSS51, PRSS55 (P328A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310733	NM_198464.4(PRSS55):c.997C>G (p.Pro333Ala)	PRSS51, PRSS55 (P333A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527418	NM_198464.4(PRSS55):c.1004C>G (p.Ser335Cys)	PRSS51, PRSS55 (S335C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 41