"ACADL-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3051681	NM_001608.4(ACADL):c.1199+9A>G	ACADL	Single nucleotide variant (intron variant)	ACADL-related condition	GLikely benign
Select item 3034814	NM_001608.4(ACADL):c.1112+5G>A	ACADL	Single nucleotide variant (intron variant)	ACADL-related condition	GLikely benign
Select item 3045444	NM_001608.4(ACADL):c.1104G>A (p.Ala368=)	ACADL	Single nucleotide variant (synonymous variant)	ACADL-related condition	GLikely benign
Select item 1701408	NM_001608.4(ACADL):c.939T>C (p.Tyr313=)	ACADL	Single nucleotide variant (synonymous variant)	ACADL-related condition +1 more	GLikely benign
Select item 2630863	NM_001608.4(ACADL):c.871-2A>G	ACADL	Single nucleotide variant (splice acceptor variant)	ACADL-related condition	GUncertain significance
Select item 3040544	NM_001608.4(ACADL):c.870+10G>A	ACADL	Single nucleotide variant (intron variant)	ACADL-related condition	GLikely benign
Select item 2634626	NM_001608.4(ACADL):c.683A>G (p.His228Arg)	ACADL (H228R)	Single nucleotide variant (missense variant)	ACADL-related condition	GUncertain significance
Select item 2571115	NM_001608.4(ACADL):c.651G>A (p.Ala217=)	ACADL	Single nucleotide variant (synonymous variant)	ACADL-related condition +1 more	GLikely benign
Select item 3042365	NM_001608.4(ACADL):c.621G>T (p.Gly207=)	ACADL	Single nucleotide variant (synonymous variant)	ACADL-related condition	GBenign
Select item 2557629	NM_001608.4(ACADL):c.508A>G (p.Ile170Val)	ACADL (I170V)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2634923	NM_001608.4(ACADL):c.497G>A (p.Cys166Tyr)	ACADL (C166Y)	Single nucleotide variant (missense variant)	ACADL-related condition	GUncertain significance
Select item 3043018	NM_001608.4(ACADL):c.372-8dup	ACADL	Duplication (intron variant)	ACADL-related condition	GBenign
Select item 3030800	NM_001608.4(ACADL):c.234-4G>A	ACADL	Single nucleotide variant (intron variant)	ACADL-related condition	GLikely benign
Select item 3029948	NM_001608.4(ACADL):c.90C>T (p.Ser30=)	ACADL	Single nucleotide variant (synonymous variant)	ACADL-related condition	GLikely benign
Select item 3035587	NM_001608.4(ACADL):c.37C>T (p.Leu13=)	ACADL	Single nucleotide variant (synonymous variant)	ACADL-related condition	GLikely benign
Select item 3032185	NM_001608.4(ACADL):c.7G>T (p.Ala3Ser)	ACADL (A3S)	Single nucleotide variant (missense variant)	ACADL-related condition	GLikely benign