"AXL-related condition"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3049243	NM_021913.5(AXL):c.36G>A (p.Pro12=)	AXL	Single nucleotide variant (synonymous variant)	AXL-related condition	GLikely benign
Select item 2894570	NM_021913.5(AXL):c.90G>A (p.Thr30=)	AXL	Single nucleotide variant (synonymous variant)	AXL-related condition +1 more	GLikely benign
Select item 752010	NM_021913.5(AXL):c.309-7C>T	AXL	Single nucleotide variant (intron variant)	AXL-related condition +1 more	GLikely benign
Select item 3040378	NM_021913.5(AXL):c.410-7C>T	AXL	Single nucleotide variant (intron variant)	AXL-related condition	GLikely benign
Select item 3043105	NM_021913.5(AXL):c.453C>T (p.Ala151=)	AXL	Single nucleotide variant (synonymous variant)	AXL-related condition	GLikely benign
Select item 3061158	NM_021913.5(AXL):c.571_572delinsCC (p.Ser191Pro)	AXL (S191P)	Indel (missense variant)	AXL-related condition	GUncertain significance
Select item 2291219	NM_021913.5(AXL):c.650G>A (p.Arg217His)	AXL (R217H)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +2 more	GUncertain significance
Select item 3050773	NM_021913.5(AXL):c.792G>A (p.Leu264=)	AXL	Single nucleotide variant (5 prime UTR variant +1 more)	AXL-related condition	GLikely benign
Select item 2918463	NM_021913.5(AXL):c.845C>T (p.Pro282Leu)	AXL (P282L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 782647	NM_021913.5(AXL):c.864C>T (p.Ser288=)	AXL	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 731261	NM_021913.5(AXL):c.984G>A (p.Thr328=)	AXL	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3047175	NM_021913.5(AXL):c.1092G>A (p.Leu364=)	AXL	Single nucleotide variant (synonymous variant)	AXL-related condition	GLikely benign
Select item 3046374	NM_021913.5(AXL):c.1189G>A (p.Gly397Arg)	AXL (G129R +1 more)	Single nucleotide variant (missense variant)	AXL-related condition	GLikely benign
Select item 2629662	NM_021913.5(AXL):c.1424G>A (p.Arg475Gln)	AXL (R207Q +2 more)	Single nucleotide variant (missense variant)	AXL-related condition	GUncertain significance
Select item 747484	NM_021913.5(AXL):c.1446-9C>T	AXL	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 2141702	NM_021913.5(AXL):c.1446-5C>G	AXL	Single nucleotide variant (intron variant)	AXL-related condition +1 more	GLikely benign
Select item 712399	NM_021913.5(AXL):c.1711+9C>T	AXL	Single nucleotide variant (intron variant)	AXL-related condition +1 more	GBenign/Likely benign
Select item 3034751	NM_021913.5(AXL):c.1803C>T (p.Ile601=)	AXL	Single nucleotide variant (synonymous variant)	AXL-related condition	GLikely benign
Select item 3038712	NM_021913.5(AXL):c.1968C>T (p.Ile656=)	AXL	Single nucleotide variant (synonymous variant)	AXL-related condition	GLikely benign
Select item 2636977	NM_021913.5(AXL):c.2209del (p.Gly736_Val737insTer)	AXL	Deletion (nonsense)	AXL-related condition	GUncertain significance
Select item 711730	NM_021913.5(AXL):c.2493T>C (p.Pro831=)	AXL	Single nucleotide variant (synonymous variant)	AXL-related condition +1 more	GBenign/Likely benign

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Items: 21