PON3[gene] and "single gene"[properties] - ClinVar

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Items: 48

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1180951	NM_000940.3(PON3):c.*29dup	PON3	Duplication (3 prime UTR variant)	not provided	GBenign
Select item 756300	NM_000940.3(PON3):c.1032C>T (p.Thr344=)	PON3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 708721	NM_000940.3(PON3):c.971G>A (p.Gly324Asp)	PON3 (G324D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2601107	NM_000940.3(PON3):c.939G>C (p.Lys313Asn)	PON3 (K313N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507980	NM_000940.3(PON3):c.916A>T (p.Ile306Phe)	PON3 (I306F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319039	NM_000940.3(PON3):c.913C>T (p.Arg305Cys)	PON3 (R305C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 732345	NM_000940.3(PON3):c.907-5G>A	PON3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1249064	NM_000940.3(PON3):c.907-230G>A	PON3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242524	NM_000940.3(PON3):c.906+42A>G	PON3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2454466	NM_000940.3(PON3):c.851A>T (p.His284Leu)	PON3 (H284L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 731879	NM_000940.3(PON3):c.816C>T (p.Val272=)	PON3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 728952	NM_000940.3(PON3):c.777+8T>C	PON3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2216710	NM_000940.3(PON3):c.773T>A (p.Leu258Gln)	PON3 (L258Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460145	NM_000940.3(PON3):c.740T>C (p.Met247Thr)	PON3 (M247T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1246197	NM_000940.3(PON3):c.696-91A>G	PON3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239780	NM_000940.3(PON3):c.695+267C>T	PON3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2276635	NM_000940.3(PON3):c.692A>G (p.Gln231Arg)	PON3 (Q231R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216762	NM_000940.3(PON3):c.676A>G (p.Thr226Ala)	PON3 (T226A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777175	NM_000940.3(PON3):c.609T>C (p.Tyr203=)	PON3	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 3216761	NM_000940.3(PON3):c.556A>T (p.Thr186Ser)	PON3 (T186S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783495	NM_000940.3(PON3):c.536C>A (p.Ala179Asp)	PON3 (A179D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 418423	NM_000940.3(PON3):c.496G>A (p.Val166Met)	PON3 (V166M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2231243	NM_000940.3(PON3):c.442C>A (p.Gln148Lys)	PON3 (Q148K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216760	NM_000940.3(PON3):c.441A>T (p.Glu147Asp)	PON3 (E147D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 711480	NM_000940.3(PON3):c.436G>A (p.Glu146Lys)	PON3 (E146K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 732851	NM_000940.3(PON3):c.427T>C (p.Phe143Leu)	PON3 (F143L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2252518	NM_000940.3(PON3):c.408G>T (p.Met136Ile)	PON3 (M136I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275916	NM_000940.3(PON3):c.406A>G (p.Met136Val)	PON3 (M136V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568771	NM_000940.3(PON3):c.388G>A (p.Val130Ile)	PON3 (V130I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1221645	NM_000940.3(PON3):c.368-113A>C	PON3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294630	NM_000940.3(PON3):c.367+127T>A	PON3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2547388	NM_000940.3(PON3):c.307A>C (p.Ser103Arg)	PON3 (S103R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1289181	NM_000940.3(PON3):c.297G>A (p.Ala99=)	PON3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2599842	NM_000940.3(PON3):c.267T>G (p.Asp89Glu)	PON3 (D89E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 799182	NM_000940.3(PON3):c.234G>T (p.Ala78=)	PON3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1289875	NM_000940.3(PON3):c.201+111C>T	PON3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3216759	NM_000940.3(PON3):c.178A>G (p.Ser60Gly)	PON3 (S60G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235273	NM_000940.3(PON3):c.155C>T (p.Ser52Phe)	PON3 (S52F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299631	NM_000940.3(PON3):c.107C>T (p.Pro36Leu)	PON3 (P36L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2657690	NM_000940.3(PON3):c.94C>G (p.Arg32Gly)	PON3 (R32G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 488870	NM_000940.3(PON3):c.94C>T (p.Arg32Ter)	PON3 (R32*)	Single nucleotide variant (nonsense)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 727834	NM_000940.3(PON3):c.84G>A (p.Val28=)	PON3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1252233	NM_000940.3(PON3):c.75-20T>C	PON3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179598	NM_000940.3(PON3):c.75-164del	PON3	Deletion (intron variant)	not provided	GBenign
Select item 1252418	NM_000940.3(PON3):c.74+136C>T	PON3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3216763	NM_000940.3(PON3):c.70T>A (p.Phe24Ile)	PON3 (F24I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1268453	NM_000940.3(PON3):c.63C>T (p.Phe21=)	PON3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 716357	NM_000940.3(PON3):c.5G>A (p.Gly2Glu)	PON3 (G2E)	Single nucleotide variant (missense variant)	not provided	GBenign

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Items: 48