Related gene-specific medical variations for Gene (Select 5644) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3222829	NM_002769.5(PRSS1):c.93G>C (p.Glu31Asp)	PRSS1, TRB (E31D)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222828	NM_002769.5(PRSS1):c.78G>A (p.Gly26=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222827	NM_002769.5(PRSS1):c.723C>T (p.Asn241=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222826	NM_002769.5(PRSS1):c.707T>G (p.Val236Gly)	PRSS1, TRB (V236G)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222825	NM_002769.5(PRSS1):c.699C>A (p.Tyr233Ter)	PRSS1, TRB (Y233*)	Single nucleotide variant (nonsense +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222824	NM_002769.5(PRSS1):c.663C>T (p.Ala221=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222822	NM_002769.5(PRSS1):c.650G>T (p.Gly217Val)	PRSS1, TRB (G217V)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222821	NM_002769.5(PRSS1):c.641T>C (p.Val214Ala)	PRSS1, TRB (V214A)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222820	NM_002769.5(PRSS1):c.636A>T (p.Gly212=)	TRB, PRSS1	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222817	NM_002769.5(PRSS1):c.55G>C (p.Asp19His)	PRSS1, TRB (D19H)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222816	NM_002769.5(PRSS1):c.557T>C (p.Val186Ala)	PRSS1, TRB (V186A)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222815	NM_002769.5(PRSS1):c.533A>G (p.Lys178Arg)	PRSS1, TRB (K178R)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222814	NM_002769.5(PRSS1):c.528T>C (p.Pro176=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222813	NM_002769.5(PRSS1):c.48C>A (p.Ala16=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222812	NM_002769.5(PRSS1):c.471G>C (p.Glu157Asp)	PRSS1, TRB (E157D)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222811	NM_002769.5(PRSS1):c.468C>A (p.Asp156Glu)	PRSS1, TRB (D156E)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222810	NM_002769.5(PRSS1):c.465A>T (p.Pro155=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222809	NM_002769.5(PRSS1):c.459C>T (p.Asp153=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222808	NM_002769.5(PRSS1):c.455-1G>A	PRSS1, TRB	Single nucleotide variant (splice acceptor variant)	Hereditary pancreatitis	GUncertain significance
Select item 3222806	NM_002769.5(PRSS1):c.395C>T (p.Pro132Leu)	PRSS1, TRB (P132L)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222805	NM_002769.5(PRSS1):c.391G>T (p.Ala131Ser)	PRSS1, TRB (A131S)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222804	NM_002769.5(PRSS1):c.387C>T (p.Pro129=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222803	NM_002769.5(PRSS1):c.371C>A (p.Ser124Tyr)	PRSS1, TRB (S124Y)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222802	NM_002769.5(PRSS1):c.370T>A (p.Ser124Thr)	PRSS1, TRB (S124T)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222801	NM_002769.5(PRSS1):c.319G>T (p.Asp107Tyr)	PRSS1, TRB (D107Y)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222800	NM_002769.5(PRSS1):c.315C>G (p.Asn105Lys)	PRSS1, TRB (N105K)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222799	NM_002769.5(PRSS1):c.310C>G (p.Leu104Val)	PRSS1, TRB (L104V)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222798	NM_002769.5(PRSS1):c.306G>T (p.Lys102Asn)	PRSS1, TRB (K102N)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222797	NM_002769.5(PRSS1):c.305A>T (p.Lys102Met)	PRSS1, TRB (K102M)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222796	NM_002769.5(PRSS1):c.305A>G (p.Lys102Arg)	PRSS1, TRB (K102R)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222795	NM_002769.5(PRSS1):c.293A>G (p.Gln98Arg)	PRSS1, TRB (Q98R)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222794	NM_002769.5(PRSS1):c.28G>A (p.Val10Met)	PRSS1, TRB (V10M)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222793	NM_002769.5(PRSS1):c.278T>C (p.Ile93Thr)	PRSS1, TRB (I93T)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222792	NM_002769.5(PRSS1):c.230A>C (p.Asn77Thr)	PRSS1, TRB (N77T)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222791	NM_002769.5(PRSS1):c.180A>G (p.Ser60=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222790	NM_002769.5(PRSS1):c.177A>C (p.Val59=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222789	NM_002769.5(PRSS1):c.149G>C (p.Gly50Ala)	PRSS1, TRB (G50A)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222788	NM_002769.5(PRSS1):c.149G>A (p.Gly50Asp)	PRSS1, TRB (G50D)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222787	NM_002769.5(PRSS1):c.145G>T (p.Gly49Cys)	PRSS1, TRB (G49C)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222786	NM_002769.5(PRSS1):c.136C>G (p.His46Asp)	PRSS1, TRB (H46D)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3222785	NM_002769.5(PRSS1):c.111C>T (p.Tyr37=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 3222784	NM_002769.5(PRSS1):c.104T>C (p.Val35Ala)	PRSS1, TRB (V35A)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 3076183	NM_002769.5(PRSS1):c.591+12_591+14del	TRB, PRSS1	Deletion (intron variant)	Hereditary pancreatitis	GUncertain significance
Select item 3015817	NM_002769.5(PRSS1):c.406G>A (p.Gly136Ser)	PRSS1, TRB (G136S)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2994198	NM_002769.5(PRSS1):c.285C>A (p.Arg95=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 2910359	NM_002769.5(PRSS1):c.653_655dup (p.Asp218_Gly219insAsp)	PRSS1, TRB	Duplication (inframe_insertion +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2899912	NM_002769.5(PRSS1):c.205A>G (p.Ile69Val)	PRSS1, TRB (I69V)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2896387	NM_002769.5(PRSS1):c.454+16A>G	PRSS1, TRB	Single nucleotide variant (intron variant)	Hereditary pancreatitis	GLikely benign
Select item 2866535	NM_002769.5(PRSS1):c.41-14C>A	PRSS1, TRB	Single nucleotide variant (intron variant)	Hereditary pancreatitis	GLikely benign
Select item 2838606	NM_002769.5(PRSS1):c.40+15C>G	PRSS1, TRB	Single nucleotide variant (intron variant)	Hereditary pancreatitis	GLikely benign
Select item 2819718	NM_002769.5(PRSS1):c.283C>A (p.Arg95Ser)	PRSS1, TRB (R95S)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2796802	NM_002769.5(PRSS1):c.592-14C>G	PRSS1, TRB	Single nucleotide variant (intron variant)	Hereditary pancreatitis	GLikely benign
Select item 2792444	NM_002769.5(PRSS1):c.625C>G (p.Gln209Glu)	PRSS1, TRB (Q209E)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary pancreatitis	GBenign
Select item 2787400	NM_002769.5(PRSS1):c.488C>T (p.Ala163Val)	PRSS1, TRB (A163V)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2785820	NM_002769.5(PRSS1):c.201-12C>T	PRSS1, TRB	Single nucleotide variant (intron variant)	Hereditary pancreatitis	GLikely benign
Select item 2761096	NM_002769.5(PRSS1):c.592-4C>T	PRSS1, TRB	Single nucleotide variant (intron variant)	Hereditary pancreatitis	GLikely benign
Select item 2737784	NM_002769.5(PRSS1):c.257A>C (p.Gln86Pro)	PRSS1, TRB (Q86P)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2735091	NM_002769.5(PRSS1):c.248G>A (p.Gly83Glu)	PRSS1, TRB (G83E)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2726145	NM_002769.5(PRSS1):c.350C>G (p.Ala117Gly)	PRSS1, TRB (A117G)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2714471	NM_002769.5(PRSS1):c.551T>C (p.Phe184Ser)	PRSS1, TRB (F184S)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2705449	NM_002769.5(PRSS1):c.619A>C (p.Asn207His)	PRSS1, TRB (N207H)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2663057	NM_002769.5(PRSS1):c.149G>T (p.Gly50Val)	PRSS1, TRB (G50V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
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 2625416	NM_002769.5(PRSS1):c.318T>A (p.Asn106Lys)	PRSS1, TRB (N106K)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2625415	NM_002769.5(PRSS1):c.560G>A (p.Gly187Asp)	PRSS1, TRB (G187D)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2625414	NM_002769.5(PRSS1):c.470A>G (p.Glu157Gly)	PRSS1, TRB (E157G)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2624548	NM_002769.5(PRSS1):c.290C>A (p.Pro97His)	PRSS1, TRB (P97H)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2624534	NM_002769.5(PRSS1):c.640G>A (p.Val214Ile)	PRSS1, TRB (V214I)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2624528	NM_002769.5(PRSS1):c.687C>T (p.Tyr229=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 2621917	NM_002769.5(PRSS1):c.86A>G (p.Asn29Ser)	PRSS1, TRB (N29S)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2621898	NM_002769.5(PRSS1):c.456C>A (p.Ala152=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2621867	NM_002769.5(PRSS1):c.667A>G (p.Lys223Glu)	PRSS1, TRB (K223E)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2621828	NM_002769.5(PRSS1):c.476A>C (p.Gln159Pro)	PRSS1, TRB (Q159P)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2621817	NM_002769.5(PRSS1):c.326T>G (p.Met109Arg)	PRSS1, TRB (M109R)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2621806	NM_002769.5(PRSS1):c.669G>A (p.Lys223=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 2584923	NM_002769.5(PRSS1):c.547A>G (p.Met183Val)	PRSS1, TRB (M183V)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2581637	NM_002769.5(PRSS1):c.1A>G (p.Met1Val)	PRSS1, TRB (M1V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2581636	NM_002769.5(PRSS1):c.1A>T (p.Met1Leu)	PRSS1, TRB (M1L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2563200	NM_002769.5(PRSS1):c.348T>G (p.Arg116=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 2563199	NM_002769.5(PRSS1):c.610G>C (p.Val204Leu)	PRSS1, TRB (V204L)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2563198	NM_002769.5(PRSS1):c.326T>C (p.Met109Thr)	PRSS1, TRB (M109T)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2563197	NM_002769.5(PRSS1):c.30G>T (p.Val10=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 2563196	NM_002769.5(PRSS1):c.332T>A (p.Ile111Asn)	PRSS1, TRB (I111N)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2563195	NM_002769.5(PRSS1):c.706G>A (p.Val236Met)	PRSS1, TRB (V236M)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2563194	NM_002769.5(PRSS1):c.602G>T (p.Gly201Val)	PRSS1, TRB (G201V)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2563193	NM_002769.5(PRSS1):c.326T>A (p.Met109Lys)	PRSS1, TRB (M109K)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2563192	NM_002769.5(PRSS1):c.428G>T (p.Gly143Val)	PRSS1, TRB (G143V)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2563191	NM_002769.5(PRSS1):c.593G>A (p.Gly198Asp)	PRSS1, TRB (G198D)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2563190	NM_002769.5(PRSS1):c.633A>G (p.Gln211=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 2563189	NM_002769.5(PRSS1):c.125A>G (p.Asn42Ser)	PRSS1, TRB (N42S)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2563188	NM_002769.5(PRSS1):c.586T>C (p.Cys196Arg)	PRSS1, TRB (C196R)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2563187	NM_002769.5(PRSS1):c.407G>T (p.Gly136Val)	PRSS1, TRB (G136V)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2563186	NM_002769.5(PRSS1):c.406G>T (p.Gly136Cys)	PRSS1, TRB (G136C)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2561593	NM_002769.5(PRSS1):c.680G>C (p.Gly227Ala)	PRSS1, TRB (G227A)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2561591	NM_002769.5(PRSS1):c.220G>A (p.Gly74Arg)	PRSS1, TRB (G74R)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2561590	NM_002769.5(PRSS1):c.695T>G (p.Val232Gly)	PRSS1, TRB (V232G)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2561589	NM_002769.5(PRSS1):c.628C>G (p.Leu210Val)	PRSS1, TRB (L210V)	Single nucleotide variant (missense variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2561588	NM_002769.5(PRSS1):c.345A>G (p.Ser115=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	Hereditary pancreatitis	GLikely benign
Select item 2560444	NM_002769.5(PRSS1):c.527del (p.Pro176fs)	PRSS1, TRB (P176fs)	Deletion (frameshift variant +1 more)	Hereditary pancreatitis	GUncertain significance
Select item 2503991	NM_002769.5(PRSS1):c.328T>C (p.Leu110=)	PRSS1, TRB	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign

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