"Ambry Genetics"[submitter] AND "PRSS27"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2608691	NM_031948.5(PRSS27):c.866A>G (p.Gln289Arg)	PRSS27 (Q187R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540179	NM_031948.5(PRSS27):c.832A>G (p.Lys278Glu)	PRSS27 (K278E +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2235798	NM_031948.5(PRSS27):c.814A>G (p.Ile272Val)	PRSS27 (I272V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219839	NM_031948.5(PRSS27):c.790C>T (p.Arg264Cys)	PRSS27 (R264C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310681	NM_031948.5(PRSS27):c.758G>A (p.Cys253Tyr)	PRSS27 (C253Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411228	NM_031948.5(PRSS27):c.652G>A (p.Glu218Lys)	PRSS27 (E116K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292389	NM_031948.5(PRSS27):c.631G>A (p.Asp211Asn)	PRSS27 (D109N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345908	NM_031948.5(PRSS27):c.607T>A (p.Tyr203Asn)	PRSS27 (Y101N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406234	NM_031948.5(PRSS27):c.544G>A (p.Ala182Thr)	PRSS27 (A182T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299899	NM_031948.5(PRSS27):c.527G>C (p.Arg176Pro)	PRSS27 (R176P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310682	NM_031948.5(PRSS27):c.491G>A (p.Gly164Asp)	PRSS27 (G164D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219838	NM_031948.5(PRSS27):c.490G>A (p.Gly164Ser)	PRSS27 (G164S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532503	NM_031948.5(PRSS27):c.463G>T (p.Gly155Cys)	PRSS27 (G53C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409049	NM_031948.5(PRSS27):c.296G>C (p.Gly99Ala)	PRSS27 (G99A)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2457882	NM_031948.5(PRSS27):c.250T>C (p.Ser84Pro)	PRSS27 (S84P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3219836	NM_031948.5(PRSS27):c.181G>T (p.Gly61Trp)	LOC130058265, PRSS27 (G61W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554106	NM_031948.5(PRSS27):c.170G>A (p.Ser57Asn)	LOC130058265, PRSS27 (S57N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622135	NM_031948.5(PRSS27):c.105G>A (p.Met35Ile)	PRSS27 (M35I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310680	NM_031948.5(PRSS27):c.49T>A (p.Ser17Thr)	PRSS27 (S17T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign