"Ambry Genetics"[submitter] AND "ATG5"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2552064	NM_004849.4(ATG5):c.679A>G (p.Ile227Val)	ATG5 (I227V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2312146	NM_004849.4(ATG5):c.559T>A (p.Phe187Ile)	ATG5 (F187I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2467725	NM_004849.4(ATG5):c.361A>G (p.Ile121Val)	ATG5 (I43V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3321384	NM_004849.4(ATG5):c.326A>G (p.Glu109Gly)	ATG5 (E31G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3131016	NM_004849.4(ATG5):c.107A>G (p.Tyr36Cys)	ATG5 (M1V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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