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

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3128184	NM_001654.5(ARAF):c.37G>A (p.Glu13Lys)	ARAF (E13K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2672157	NM_001654.5(ARAF):c.97-7C>T	ARAF	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2660426	NM_001654.5(ARAF):c.126C>T (p.Tyr42=)	ARAF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3128183	NM_001654.5(ARAF):c.329C>T (p.Ala110Val)	ARAF (A110V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353940	NM_001654.5(ARAF):c.449A>G (p.Asn150Ser)	ARAF (N150S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3128185	NM_001654.5(ARAF):c.451C>T (p.Arg151Cys)	ARAF (R151C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260066	NM_001654.5(ARAF):c.484T>C (p.Ser162Pro)	ARAF (S162P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526648	NM_001654.5(ARAF):c.498A>T (p.Arg166Ser)	ARAF (R169S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276500	NM_001654.5(ARAF):c.515C>T (p.Ser172Leu)	ARAF (S172L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284075	NM_001654.5(ARAF):c.542C>A (p.Thr181Asn)	ARAF (T184N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511522	NM_001654.5(ARAF):c.571C>T (p.His191Tyr)	ARAF (H194Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402017	NM_001654.5(ARAF):c.599C>G (p.Pro200Arg)	ARAF (P203R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 376367	NM_001654.5(ARAF):c.640T>G (p.Ser214Ala)	ARAF (S214A +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma, sporadic +2 more	GLikely pathogenic
Select item 376366	NM_001654.5(ARAF):c.641C>T (p.Ser214Phe)	ARAF (S214F +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma, sporadic +2 more	GLikely pathogenic
Select item 376137	NM_001654.5(ARAF):c.641C>G (p.Ser214Cys)	ARAF (S214C +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma, sporadic +2 more	GLikely pathogenic
Select item 2496248	NM_001654.5(ARAF):c.650A>G (p.Asn217Ser)	ARAF (N217S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492782	NM_001654.5(ARAF):c.696C>G (p.Ile232Met)	ARAF (I232M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363358	NM_001654.5(ARAF):c.785G>T (p.Ser262Ile)	ARAF (S262I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3128187	NM_001654.5(ARAF):c.808C>G (p.Pro270Ala)	ARAF (P270A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2660427	NM_001654.5(ARAF):c.855C>T (p.Ala285=)	ARAF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2672194	NM_001654.5(ARAF):c.934C>G (p.Leu312Val)	ARAF (L312V +1 more)	Single nucleotide variant (missense variant)	ARAF-related disorder	GUncertain significance
Select item 3128188	NM_001654.5(ARAF):c.998T>C (p.Val333Ala)	ARAF (V336A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 789251	NM_001654.5(ARAF):c.1002C>T (p.Ala334=)	ARAF	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3128181	NM_001654.5(ARAF):c.1106T>G (p.Phe369Cys)	ARAF (F369C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527603	NM_001654.5(ARAF):c.1183C>T (p.His395Tyr)	ARAF (H395Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340064	NM_001654.5(ARAF):c.1232G>A (p.Arg411Gln)	ARAF (R411Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 713393	NM_001654.5(ARAF):c.1413G>A (p.Leu471=)	ARAF	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2256538	NM_001654.5(ARAF):c.1509G>A (p.Met503Ile)	ARAF (M506I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3128182	NM_001654.5(ARAF):c.1528A>G (p.Ser510Gly)	ARAF (S510G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 747628	NM_001654.5(ARAF):c.1734G>C (p.Glu578Asp)	ARAF (E581D +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign

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Items: 30