ACSS1[gene] and "single gene"[properties] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2221832	NM_032501.4(ACSS1):c.2014G>A (p.Ala672Thr)	ACSS1 (A670T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2601840	NM_032501.4(ACSS1):c.2006G>C (p.Ser669Thr)	ACSS1 (S548T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2367754	NM_032501.4(ACSS1):c.2002C>T (p.Pro668Ser)	ACSS1 (P547S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214796	NM_032501.4(ACSS1):c.1985C>T (p.Thr662Ile)	ACSS1 (T541I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140874	NM_032501.4(ACSS1):c.1961G>T (p.Ser654Ile)	ACSS1 (S533I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140872	NM_032501.4(ACSS1):c.1838A>G (p.Lys613Arg)	ACSS1 (K492R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2600364	NM_032501.4(ACSS1):c.1805C>T (p.Ala602Val)	ACSS1 (A481V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370505	NM_032501.4(ACSS1):c.1790T>G (p.Val597Gly)	ACSS1 (V595G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140863	NM_032501.4(ACSS1):c.1770A>T (p.Glu590Asp)	ACSS1 (E469D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2260647	NM_032501.4(ACSS1):c.1675C>T (p.Arg559Trp)	ACSS1 (R438W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140858	NM_032501.4(ACSS1):c.1595G>A (p.Gly532Glu)	ACSS1 (G530E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140855	NM_032501.4(ACSS1):c.1556A>G (p.Asp519Gly)	ACSS1 (D519G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294923	NM_032501.4(ACSS1):c.1547G>T (p.Arg516Leu)	ACSS1 (R514L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459106	NM_032501.4(ACSS1):c.1477G>A (p.Val493Ile)	ACSS1 (V491I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1258805	NM_032501.4(ACSS1):c.1435G>A (p.Val479Ile)	ACSS1 (V358I +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3140845	NM_032501.4(ACSS1):c.1360G>A (p.Ala454Thr)	ACSS1 (A454T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560811	NM_032501.4(ACSS1):c.1213T>C (p.Tyr405His)	ACSS1 (Y284H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2652247	NM_032501.4(ACSS1):c.1209G>A (p.Lys403=)	ACSS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3140835	NM_032501.4(ACSS1):c.1175G>A (p.Arg392Gln)	ACSS1 (R271Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480505	NM_032501.4(ACSS1):c.1046G>C (p.Gly349Ala)	ACSS1 (G228A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393583	NM_032501.4(ACSS1):c.946G>A (p.Ala316Thr)	ACSS1 (A316T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140905	NM_032501.4(ACSS1):c.835G>A (p.Ala279Thr)	ACSS1 (A158T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285074	NM_032501.4(ACSS1):c.797C>T (p.Pro266Leu)	ACSS1 (P145L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285828	NM_032501.4(ACSS1):c.733G>A (p.Val245Met)	ACSS1 (V245M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223258	NM_032501.4(ACSS1):c.661C>G (p.Gln221Glu)	ACSS1 (Q221E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140893	NM_032501.4(ACSS1):c.580G>A (p.Val194Ile)	ACSS1 (V194I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393344	NM_032501.4(ACSS1):c.520G>A (p.Val174Met)	ACSS1 (V174M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623751	NM_032501.4(ACSS1):c.434A>G (p.Glu145Gly)	ACSS1 (E145G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2652248	NM_032501.4(ACSS1):c.432-1425C>T	ACSS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2509771	NM_032501.4(ACSS1):c.394C>T (p.Arg132Cys)	ACSS1 (R132C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396087	NM_032501.4(ACSS1):c.376G>A (p.Val126Ile)	ACSS1 (V126I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3140842	NM_032501.4(ACSS1):c.132C>A (p.Ser44Arg)	ACSS1 (S44R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140916	NM_032501.4(ACSS1):c.96C>A (p.Ser32Arg)	ACSS1 (S32R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140909	NM_032501.4(ACSS1):c.88G>C (p.Gly30Arg)	ACSS1 (G30R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 34