ACSL1[gene] and "single gene"[properties] - ClinVar

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Items: 42

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3139865	NM_001995.5(ACSL1):c.2044C>T (p.Arg682Trp)	ACSL1 (R633W +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139862	NM_001995.5(ACSL1):c.1924G>C (p.Gly642Arg)	ACSL1 (G608R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 717920	NM_001995.5(ACSL1):c.1905C>T (p.Leu635=)	ACSL1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2259430	NM_001995.5(ACSL1):c.1846G>A (p.Gly616Arg)	ACSL1 (G552R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139853	NM_001995.5(ACSL1):c.1726A>G (p.Ile576Val)	ACSL1 (I512V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2396165	NM_001995.5(ACSL1):c.1718T>C (p.Ile573Thr)	ACSL1 (I509T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466068	NM_001995.5(ACSL1):c.1706C>T (p.Ala569Val)	ACSL1 (A505V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361229	NM_001995.5(ACSL1):c.1702A>G (p.Ile568Val)	ACSL1 (I568V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262837	NM_001995.5(ACSL1):c.1616G>A (p.Gly539Glu)	ACSL1 (G490E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 773712	NM_001995.5(ACSL1):c.1518C>T (p.Gly506=)	ACSL1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2406583	NM_001995.5(ACSL1):c.1444G>A (p.Ala482Thr)	ACSL1 (A418T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262832	NM_001995.5(ACSL1):c.1433G>C (p.Gly478Ala)	ACSL1 (G444A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2516201	NM_001995.5(ACSL1):c.1429G>A (p.Ala477Thr)	ACSL1 (A413T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262809	NM_001995.5(ACSL1):c.1396G>A (p.Gly466Arg)	ACSL1 (G466R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239387	NM_001995.5(ACSL1):c.1388G>A (p.Cys463Tyr)	ACSL1 (C399Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325235	NM_001995.5(ACSL1):c.1343C>T (p.Ala448Val)	ACSL1 (A399V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615222	NM_001995.5(ACSL1):c.1331C>T (p.Thr444Met)	ACSL1 (T444M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139789	NM_001995.5(ACSL1):c.1303G>A (p.Ala435Thr)	ACSL1 (A386T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262817	NM_001995.5(ACSL1):c.1285C>T (p.Arg429Trp)	ACSL1 (R365W +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262800	NM_001995.5(ACSL1):c.1265C>T (p.Ser422Leu)	ACSL1 (S358L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489078	NM_001995.5(ACSL1):c.1225A>C (p.Asn409His)	ACSL1 (N375H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262804	NM_001995.5(ACSL1):c.1150A>G (p.Thr384Ala)	ACSL1 (T335A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368738	NM_001995.5(ACSL1):c.1127G>A (p.Arg376Gln)	ACSL1 (R312Q +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2308200	NM_001995.5(ACSL1):c.989T>C (p.Val330Ala)	ACSL1 (V281A +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3139914	NM_001995.5(ACSL1):c.877A>G (p.Ile293Val)	ACSL1 (I229V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3139910	NM_001995.5(ACSL1):c.872G>A (p.Arg291Gln)	ACSL1 (R257Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3139900	NM_001995.5(ACSL1):c.769G>A (p.Ala257Thr)	ACSL1 (A257T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620208	NM_001995.5(ACSL1):c.717G>C (p.Gln239His)	ACSL1 (Q190H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213437	NM_001995.5(ACSL1):c.710G>A (p.Arg237Gln)	ACSL1 (R203Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404201	NM_001995.5(ACSL1):c.692G>T (p.Gly231Val)	ACSL1 (G182V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262823	NM_001995.5(ACSL1):c.691G>A (p.Gly231Ser)	ACSL1 (G231S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 787616	NM_001995.5(ACSL1):c.627A>G (p.Leu209=)	ACSL1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2219173	NM_001995.5(ACSL1):c.523G>A (p.Val175Ile)	ACSL1 (V175I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358347	NM_001995.5(ACSL1):c.521T>G (p.Ile174Ser)	ACSL1 (I125S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454478	NM_001995.5(ACSL1):c.434C>T (p.Ala145Val)	ACSL1 (A96V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2541962	NM_001995.5(ACSL1):c.430A>G (p.Thr144Ala)	ACSL1 (T80A +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3139869	NM_001995.5(ACSL1):c.218C>G (p.Ser73Cys)	ACSL1 (S9C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2242184	NM_001995.5(ACSL1):c.148C>G (p.Pro50Ala)	ACSL1 (P50A)	Single nucleotide variant (missense variant +3 more)	not specified	GLikely benign
Select item 2655208	NM_001995.5(ACSL1):c.132C>T (p.Tyr44=)	ACSL1	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 3139902	NM_001995.5(ACSL1):c.77C>T (p.Pro26Leu)	ACSL1 (P26L)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3139887	NM_001995.5(ACSL1):c.67C>A (p.Arg23Ser)	ACSL1 (R23S)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3139884	NM_001995.5(ACSL1):c.64G>A (p.Val22Met)	ACSL1 (V22M)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance

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Items: 42