"Ambry Genetics"[submitter] AND "MAGIX"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2406633	NM_024859.4(MAGIX):c.50G>A (p.Gly17Asp)	LOC130068275, MAGIX (G17D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122298	NM_024859.4(MAGIX):c.65C>G (p.Pro22Arg)	LOC130068275, MAGIX (P22R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2599382	NM_024859.4(MAGIX):c.101G>T (p.Arg34Leu)	LOC130068275, MAGIX (R34L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491461	NM_024859.4(MAGIX):c.149C>A (p.Ala50Glu)	MAGIX (A50E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540087	NM_024859.4(MAGIX):c.167G>A (p.Gly56Asp)	MAGIX (G56D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306427	NM_024859.4(MAGIX):c.195G>C (p.Glu65Asp)	MAGIX (E65D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244274	NM_024859.4(MAGIX):c.254C>T (p.Ala85Val)	MAGIX (A85V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210225	NM_024859.4(MAGIX):c.305C>T (p.Ala102Val)	MAGIX (A102V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122294	NM_024859.4(MAGIX):c.417A>C (p.Leu139Phe)	MAGIX (L139F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122295	NM_024859.4(MAGIX):c.419G>A (p.Gly140Asp)	MAGIX (G140D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122296	NM_024859.4(MAGIX):c.491G>A (p.Arg164His)	MAGIX (R164H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602652	NM_024859.4(MAGIX):c.616C>T (p.Arg206Cys)	MAGIX (R130C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122297	NM_024859.4(MAGIX):c.617G>A (p.Arg206His)	MAGIX (R147H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225903	NM_024859.4(MAGIX):c.646C>G (p.Pro216Ala)	MAGIX (P140A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122299	NM_024859.4(MAGIX):c.854C>G (p.Pro285Arg)	LOC119407416, MAGIX (P226R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224783	NM_024859.4(MAGIX):c.875C>T (p.Pro292Leu)	LOC119407416, MAGIX (P211L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489723	NM_024859.4(MAGIX):c.917C>T (p.Pro306Leu)	LOC119407416, MAGIX (P225L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance