ClinVar for Gene (Select 100129029) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3307148	NM_003628.6(PKP4):c.2661A>C (p.Arg887Ser)	PKP4, PKP4-AS1 (R886S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307145	NM_003628.6(PKP4):c.2282G>A (p.Arg761Gln)	PKP4, PKP4-AS1 (R418Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307144	NM_003628.6(PKP4):c.2984G>A (p.Arg995Gln)	PKP4, PKP4-AS1 (R994Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307142	NM_003628.6(PKP4):c.3071A>G (p.Lys1024Arg)	PKP4, PKP4-AS1 (K681R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307139	NM_003628.6(PKP4):c.2556C>T (p.Asn852=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3307137	NM_003628.6(PKP4):c.2775T>G (p.Asn925Lys)	PKP4, PKP4-AS1 (N922K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307132	NM_003628.6(PKP4):c.3492G>A (p.Ser1164=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3307131	NM_003628.6(PKP4):c.2580T>G (p.Phe860Leu)	PKP4, PKP4-AS1 (F858L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307128	NM_003628.6(PKP4):c.3182A>G (p.Glu1061Gly)	PKP4, PKP4-AS1 (E718G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3307127	NM_003628.6(PKP4):c.3083C>T (p.Ser1028Phe)	PKP4, PKP4-AS1 (S1025F +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307126	NM_003628.6(PKP4):c.3271T>C (p.Ser1091Pro)	PKP4, PKP4-AS1 (S1047P +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307125	NM_003628.6(PKP4):c.2338G>A (p.Asp780Asn)	PKP4, PKP4-AS1 (D777N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307124	NM_003628.6(PKP4):c.2435C>T (p.Ser812Leu)	PKP4, PKP4-AS1 (S811L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307122	NM_003628.6(PKP4):c.3018G>C (p.Trp1006Cys)	PKP4, PKP4-AS1 (W1004C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307117	NM_003628.6(PKP4):c.2123G>A (p.Arg708Gln)	PKP4, PKP4-AS1 (R365Q +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3223528	NM_003628.6(PKP4):c.3480T>C (p.Tyr1160=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3223527	NM_003628.6(PKP4):c.3401A>G (p.Gln1134Arg)	PKP4, PKP4-AS1 (Q1090R +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223526	NM_003628.6(PKP4):c.3376T>A (p.Phe1126Ile)	PKP4-AS1, PKP4 (F1082I +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223525	NM_003628.6(PKP4):c.3358G>A (p.Asp1120Asn)	PKP4, PKP4-AS1 (D1076N +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223524	NM_003628.6(PKP4):c.3341T>C (p.Leu1114Pro)	PKP4, PKP4-AS1 (L1070P +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223523	NM_003628.6(PKP4):c.3245G>T (p.Gly1082Val)	PKP4-AS1, PKP4 (G1079V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3223522	NM_003628.6(PKP4):c.3194C>T (p.Thr1065Ile)	PKP4, PKP4-AS1 (T1062I +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3223521	NM_003628.6(PKP4):c.3154C>G (p.Leu1052Val)	PKP4, PKP4-AS1 (L1049V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3223520	NM_003628.6(PKP4):c.3134G>C (p.Ser1045Thr)	PKP4-AS1, PKP4 (S1042T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3223519	NM_003628.6(PKP4):c.2996G>A (p.Ser999Asn)	PKP4, PKP4-AS1 (S656N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223518	NM_003628.6(PKP4):c.2930C>A (p.Ser977Tyr)	PKP4, PKP4-AS1 (S634Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223517	NM_003628.6(PKP4):c.2919C>T (p.Gly973=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3223516	NM_003628.6(PKP4):c.2877A>G (p.Ser959=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3223514	NM_003628.6(PKP4):c.2763C>T (p.Leu921=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3223513	NM_003628.6(PKP4):c.2758C>G (p.Arg920Gly)	PKP4, PKP4-AS1 (R577G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223512	NM_003628.6(PKP4):c.2744G>A (p.Arg915Gln)	PKP4, PKP4-AS1 (R572Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223511	NM_003628.6(PKP4):c.2707G>T (p.Val903Phe)	PKP4, PKP4-AS1 (V560F +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223510	NM_003628.6(PKP4):c.2620C>T (p.Leu874Phe)	PKP4, PKP4-AS1 (L531F +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223509	NM_003628.6(PKP4):c.2601C>T (p.Ala867=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3223508	NM_003628.6(PKP4):c.2534G>C (p.Gly845Ala)	PKP4, PKP4-AS1 (G502A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223507	NM_003628.6(PKP4):c.2522C>T (p.Ala841Val)	PKP4, PKP4-AS1 (A498V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223506	NM_003628.6(PKP4):c.2479G>A (p.Val827Ile)	PKP4, PKP4-AS1 (V484I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223505	NM_003628.6(PKP4):c.2478G>A (p.Val826=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3223504	NM_003628.6(PKP4):c.2390C>T (p.Pro797Leu)	PKP4, PKP4-AS1 (P454L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223503	NM_003628.6(PKP4):c.2263C>G (p.Leu755Val)	PKP4, PKP4-AS1 (L412V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223502	NM_003628.6(PKP4):c.2190C>T (p.Asn730=)	PKP4, PKP4-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3223501	NM_003628.6(PKP4):c.2181G>A (p.Thr727=)	PKP4, PKP4-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3223499	NM_003628.6(PKP4):c.2163G>A (p.Leu721=)	PKP4, PKP4-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3223498	NM_003628.6(PKP4):c.2103C>T (p.Ser701=)	PKP4, PKP4-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3214031	NM_003628.6(PKP4):c.3230A>C (p.Asp1077Ala)	PKP4, PKP4-AS1 (D1076A +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3214030	NM_003628.6(PKP4):c.2376G>C (p.Lys792Asn)	PKP4, PKP4-AS1 (K791N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214029	NM_003628.6(PKP4):c.2375A>C (p.Lys792Thr)	PKP4, PKP4-AS1 (K790T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214028	NM_003628.6(PKP4):c.2298C>A (p.Asn766Lys)	PKP4, PKP4-AS1 (N764K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214027	NM_003628.6(PKP4):c.2197G>A (p.Asp733Asn)	PKP4, PKP4-AS1 (D390N +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2681489	NM_003628.6(PKP4):c.2974T>C (p.Trp992Arg)	PKP4, PKP4-AS1 (W649R +4 more)	Single nucleotide variant (missense variant)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2625294	NM_003628.6(PKP4):c.2879G>A (p.Gly960Glu)	PKP4, PKP4-AS1 (G617E +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2625293	NM_003628.6(PKP4):c.3299C>T (p.Ser1100Leu)	PKP4, PKP4-AS1 (S1056L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2625292	NM_003628.6(PKP4):c.2254C>T (p.Arg752Trp)	PKP4, PKP4-AS1 (R751W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2625289	NM_003628.6(PKP4):c.2524A>T (p.Thr842Ser)	PKP4, PKP4-AS1 (T841S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2625287	NM_003628.6(PKP4):c.2268G>A (p.Glu756=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2625283	NM_003628.6(PKP4):c.2552A>G (p.Gln851Arg)	PKP4, PKP4-AS1 (Q850R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620901	NM_003628.6(PKP4):c.2758C>T (p.Arg920Trp)	PKP4, PKP4-AS1 (R577W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607973	NM_003628.6(PKP4):c.2766C>T (p.Pro922=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2607771	NM_003628.6(PKP4):c.2328T>C (p.Ser776=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2563020	NM_003628.6(PKP4):c.3345T>C (p.Tyr1115=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2563019	NM_003628.6(PKP4):c.3460A>G (p.Thr1154Ala)	PKP4, PKP4-AS1 (T1110A +6 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2563017	NM_003628.6(PKP4):c.3253C>T (p.Pro1085Ser)	PKP4, PKP4-AS1 (P1082S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2563013	NM_003628.6(PKP4):c.2115A>T (p.Glu705Asp)	PKP4, PKP4-AS1 (E702D +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2563011	NM_003628.6(PKP4):c.2700A>G (p.Ala900=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2563010	NM_003628.6(PKP4):c.2710C>T (p.Arg904Cys)	PKP4, PKP4-AS1 (R902C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2563008	NM_003628.6(PKP4):c.2631T>C (p.Leu877=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2561561	NM_003628.6(PKP4):c.2458A>G (p.Met820Val)	PKP4, PKP4-AS1 (M819V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561560	NM_003628.6(PKP4):c.2291G>C (p.Gly764Ala)	PKP4, PKP4-AS1 (G762A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561555	NM_003628.6(PKP4):c.2129A>G (p.Gln710Arg)	PKP4, PKP4-AS1 (Q367R +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2561553	NM_003628.6(PKP4):c.2661A>T (p.Arg887Ser)	PKP4, PKP4-AS1 (R544S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561552	NM_003628.6(PKP4):c.2525C>T (p.Thr842Ile)	PKP4, PKP4-AS1 (T499I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561551	NM_003628.6(PKP4):c.2484A>G (p.Lys828=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2560404	NM_003628.6(PKP4):c.2764C>T (p.Pro922Ser)	PKP4, PKP4-AS1 (P579S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560403	NM_003628.6(PKP4):c.2514C>T (p.Ser838=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2560401	NM_003628.6(PKP4):c.2472A>T (p.Pro824=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2540484	NM_003628.6(PKP4):c.3284T>C (p.Ile1095Thr)	PKP4, PKP4-AS1 (I1095T +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496860	NM_003628.6(PKP4):c.3544G>A (p.Glu1182Lys)	PKP4, PKP4-AS1 (E1139K +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489940	NM_003628.6(PKP4):c.2437A>C (p.Lys813Gln)	PKP4, PKP4-AS1 (K810Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489832	NM_003628.6(PKP4):c.2232C>T (p.Cys744=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2489726	NM_003628.6(PKP4):c.3052T>C (p.Leu1018=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 2489409	NM_003628.6(PKP4):c.3150A>G (p.Pro1050=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2489308	NM_003628.6(PKP4):c.2550C>T (p.Leu850=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2489208	NM_003628.6(PKP4):c.3147A>G (p.Ser1049=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2489110	NM_003628.6(PKP4):c.3527G>A (p.Arg1176Gln)	PKP4, PKP4-AS1 (R1173Q +6 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2489013	NM_003628.6(PKP4):c.2180C>T (p.Thr727Met)	PKP4, PKP4-AS1 (T384M +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2448036	NM_003628.6(PKP4):c.3068T>G (p.Phe1023Cys)	PKP4, PKP4-AS1 (F1021C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2448034	NM_003628.6(PKP4):c.2148G>T (p.Gly716=)	PKP4, PKP4-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2448033	NM_003628.6(PKP4):c.2612A>G (p.Glu871Gly)	PKP4, PKP4-AS1 (E868G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2448032	NM_003628.6(PKP4):c.2454T>G (p.Val818=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2448030	NM_003628.6(PKP4):c.3210G>A (p.Gln1070=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2448024	NM_003628.6(PKP4):c.2992C>T (p.Arg998Trp)	PKP4, PKP4-AS1 (R996W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2448018	NM_003628.6(PKP4):c.2601C>G (p.Ala867=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2448017	NM_003628.6(PKP4):c.2361G>A (p.Gly787=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2448016	NM_003628.6(PKP4):c.3512T>C (p.Phe1171Ser)	PKP4, PKP4-AS1 (F1127S +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2448015	NM_003628.6(PKP4):c.3319A>C (p.Arg1107=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2448014	NM_003628.6(PKP4):c.2236C>T (p.Leu746=)	PKP4, PKP4-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2332225	NM_003628.6(PKP4):c.3275C>G (p.Pro1092Arg)	PKP4, PKP4-AS1 (P1049R +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279407	NM_003628.6(PKP4):c.2527T>G (p.Leu843Val)	PKP4, PKP4-AS1 (L842V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277472	NM_003628.6(PKP4):c.2848A>T (p.Met950Leu)	PKP4, PKP4-AS1 (M948L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246347	NM_003628.6(PKP4):c.2252A>G (p.Tyr751Cys)	PKP4, PKP4-AS1 (Y751C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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