PLIN2[gene] and "single gene"[properties] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2336431	NM_001122.4(PLIN2):c.1289A>T (p.Gln430Leu)	PLIN2 (Q430L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3307741	NM_001122.4(PLIN2):c.1195A>G (p.Asn399Asp)	PLIN2 (N399D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3215236	NM_001122.4(PLIN2):c.1192C>G (p.Leu398Val)	PLIN2 (L398V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3215235	NM_001122.4(PLIN2):c.1165A>G (p.Met389Val)	PLIN2 (M389V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3215234	NM_001122.4(PLIN2):c.1129C>A (p.Gln377Lys)	PLIN2 (Q377K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526930	NM_001122.4(PLIN2):c.992A>T (p.Asn331Ile)	PLIN2 (N331I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 782857	NM_001122.4(PLIN2):c.971C>T (p.Thr324Met)	PLIN2 (T324M)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2295320	NM_001122.4(PLIN2):c.928A>G (p.Thr310Ala)	PLIN2 (T310A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2387563	NM_001122.4(PLIN2):c.926G>A (p.Arg309His)	PLIN2 (R309H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3307742	NM_001122.4(PLIN2):c.907G>A (p.Ala303Thr)	PLIN2 (A303T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3215243	NM_001122.4(PLIN2):c.878G>A (p.Gly293Glu)	PLIN2 (G293E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2203951	NM_001122.4(PLIN2):c.844T>C (p.Tyr282His)	PLIN2 (Y282H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3215242	NM_001122.4(PLIN2):c.808G>C (p.Ala270Pro)	PLIN2 (A270P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491690	NM_001122.4(PLIN2):c.784T>C (p.Phe262Leu)	PLIN2 (F262L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279355	NM_001122.4(PLIN2):c.728A>G (p.Lys243Arg)	PLIN2 (K243R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331472	NM_001122.4(PLIN2):c.656G>A (p.Arg219Lys)	PLIN2 (R219K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2266752	NM_001122.4(PLIN2):c.644G>C (p.Ser215Thr)	PLIN2 (S215T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484845	NM_001122.4(PLIN2):c.640C>G (p.Pro214Ala)	PLIN2 (P214A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3215241	NM_001122.4(PLIN2):c.626A>T (p.Asp209Val)	PLIN2 (D209V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542102	NM_001122.4(PLIN2):c.538C>G (p.Leu180Val)	PLIN2 (L180V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 723590	NM_001122.4(PLIN2):c.493G>C (p.Gly165Arg)	PLIN2 (G165R)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 3215240	NM_001122.4(PLIN2):c.398C>T (p.Thr133Met)	PLIN2 (T133M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3215239	NM_001122.4(PLIN2):c.374G>A (p.Gly125Glu)	PLIN2 (G125E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3215238	NM_001122.4(PLIN2):c.272A>C (p.Glu91Ala)	PLIN2 (E91A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2560940	NM_001122.4(PLIN2):c.242C>T (p.Thr81Ile)	PLIN2 (T81I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3215237	NM_001122.4(PLIN2):c.206T>C (p.Ile69Thr)	PLIN2 (I69T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238714	NM_001122.4(PLIN2):c.53A>G (p.Asn18Ser)	PLIN2 (N18S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 27