PLA2G4C[gene] and "single gene"[properties] - ClinVar

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Items: 56

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2356947	NM_003706.3(PLA2G4C):c.1621G>A (p.Ala541Thr)	PLA2G4C (A541T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590651	NM_003706.3(PLA2G4C):c.1579G>A (p.Gly527Arg)	PLA2G4C (G527R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240726	NM_003706.3(PLA2G4C):c.1577C>A (p.Ala526Asp)	PLA2G4C (A526D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257708	NM_003706.3(PLA2G4C):c.1540A>G (p.Asn514Asp)	PLA2G4C (N514D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365812	NM_003706.3(PLA2G4C):c.1510T>G (p.Leu504Val)	PLA2G4C (L514V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214100	NM_003706.3(PLA2G4C):c.1463C>T (p.Thr488Ile)	PLA2G4C (T488I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307178	NM_003706.3(PLA2G4C):c.1459G>A (p.Asp487Asn)	PLA2G4C (D487N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294526	NM_003706.3(PLA2G4C):c.1440G>T (p.Glu480Asp)	PLA2G4C (E480D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214099	NM_003706.3(PLA2G4C):c.1420G>T (p.Ala474Ser)	PLA2G4C (A484S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371665	NM_003706.3(PLA2G4C):c.1395G>A (p.Met465Ile)	PLA2G4C (M465I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543430	NM_003706.3(PLA2G4C):c.1354A>G (p.Ser452Gly)	PLA2G4C (S452G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214098	NM_003706.3(PLA2G4C):c.1318G>A (p.Glu440Lys)	PLA2G4C (E450K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376299	NM_003706.3(PLA2G4C):c.1265G>A (p.Arg422Gln)	PLA2G4C (R422Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214097	NM_003706.3(PLA2G4C):c.1076C>T (p.Thr359Ile)	PLA2G4C (T369I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310276	NM_003706.3(PLA2G4C):c.1062G>C (p.Lys354Asn)	PLA2G4C (K364N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214096	NM_003706.3(PLA2G4C):c.1054G>A (p.Ala352Thr)	PLA2G4C (A362T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214095	NM_003706.3(PLA2G4C):c.1018A>G (p.Asn340Asp)	PLA2G4C (N340D +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3214114	NM_003706.3(PLA2G4C):c.955A>G (p.Arg319Gly)	PLA2G4C (R329G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 788028	NM_003706.3(PLA2G4C):c.948T>C (p.Asn316=)	PLA2G4C	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3214113	NM_003706.3(PLA2G4C):c.943G>A (p.Glu315Lys)	PLA2G4C (E325K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345304	NM_003706.3(PLA2G4C):c.907G>A (p.Gly303Ser)	PLA2G4C (G313S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214112	NM_003706.3(PLA2G4C):c.904G>A (p.Gly302Ser)	PLA2G4C (G312S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325402	NM_003706.3(PLA2G4C):c.889C>T (p.Pro297Ser)	PLA2G4C (P297S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307181	NM_003706.3(PLA2G4C):c.866A>T (p.Glu289Val)	PLA2G4C (E299V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214111	NM_003706.3(PLA2G4C):c.866A>G (p.Glu289Gly)	PLA2G4C (E289G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307183	NM_003706.3(PLA2G4C):c.848G>T (p.Arg283Leu)	PLA2G4C (R293L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307179	NM_003706.3(PLA2G4C):c.848G>A (p.Arg283Gln)	PLA2G4C (R283Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214110	NM_003706.3(PLA2G4C):c.830G>A (p.Gly277Glu)	PLA2G4C (G277E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214109	NM_003706.3(PLA2G4C):c.827T>C (p.Ile276Thr)	PLA2G4C (I286T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307182	NM_003706.3(PLA2G4C):c.820A>G (p.Lys274Glu)	PLA2G4C (K274E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331804	NM_003706.3(PLA2G4C):c.800G>A (p.Arg267Lys)	PLA2G4C (R267K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297289	NM_003706.3(PLA2G4C):c.665G>C (p.Arg222Thr)	PLA2G4C (R222T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508189	NM_003706.3(PLA2G4C):c.642C>A (p.Phe214Leu)	PLA2G4C (F224L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346244	NM_003706.3(PLA2G4C):c.637C>T (p.His213Tyr)	PLA2G4C (H213Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546560	NM_003706.3(PLA2G4C):c.611C>T (p.Ala204Val)	PLA2G4C (A214V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214108	NM_003706.3(PLA2G4C):c.542C>G (p.Pro181Arg)	PLA2G4C (P181R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406177	NM_003706.3(PLA2G4C):c.542C>A (p.Pro181His)	PLA2G4C (P181H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 717091	NM_003706.3(PLA2G4C):c.481C>G (p.Pro161Ala)	PLA2G4C (P161A +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3214107	NM_003706.3(PLA2G4C):c.475A>G (p.Lys159Glu)	PLA2G4C (K159E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307177	NM_003706.3(PLA2G4C):c.416C>T (p.Ala139Val)	PLA2G4C (A149V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 784834	NM_003706.3(PLA2G4C):c.399T>C (p.Ser133=)	PLA2G4C	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3214106	NM_003706.3(PLA2G4C):c.323G>A (p.Arg108Gln)	PLA2G4C (R108Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214105	NM_003706.3(PLA2G4C):c.263T>C (p.Ile88Thr)	PLA2G4C (I88T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214104	NM_003706.3(PLA2G4C):c.262A>G (p.Ile88Val)	PLA2G4C (I88V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610829	NM_003706.3(PLA2G4C):c.250T>A (p.Ser84Thr)	PLA2G4C (S94T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252046	NM_003706.3(PLA2G4C):c.248G>A (p.Gly83Glu)	PLA2G4C (G93E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245577	NM_003706.3(PLA2G4C):c.227C>T (p.Thr76Met)	PLA2G4C (T76M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404563	NM_003706.3(PLA2G4C):c.223G>A (p.Val75Ile)	PLA2G4C (V75I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214103	NM_003706.3(PLA2G4C):c.184G>T (p.Val62Phe)	PLA2G4C (V72F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307176	NM_003706.3(PLA2G4C):c.151G>A (p.Gly51Arg)	PLA2G4C (G61R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319009	NM_003706.3(PLA2G4C):c.142G>T (p.Gly48Cys)	PLA2G4C (G48C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307180	NM_003706.3(PLA2G4C):c.66A>T (p.Arg22Ser)	PLA2G4C (R22S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337152	NM_003706.3(PLA2G4C):c.53C>T (p.Ala18Val)	PLA2G4C (A18V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2405561	NM_003706.3(PLA2G4C):c.46G>C (p.Glu16Gln)	PLA2G4C (E16Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2681491	NM_003706.3(PLA2G4C):c.29C>T (p.Pro10Leu)	PLA2G4C (P10L)	Single nucleotide variant (missense variant +1 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 3214101	NM_003706.3(PLA2G4C):c.14A>C (p.Glu5Ala)	PLA2G4C (E5A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 56