Related gene-specific medical variations for Gene (Select 28956) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2868965	NM_014017.4(LAMTOR2):c.213C>A (p.Phe71Leu)	LAMTOR2, LOC129931594 (F71L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2794069	NM_014017.4(LAMTOR2):c.187G>A (p.Ala63Thr)	LAMTOR2, LOC129931594 (A63T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2121622	NM_014017.4(LAMTOR2):c.174del (p.Asn59fs)	LAMTOR2, LOC129931594 (N59fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 1921611	NM_014017.4(LAMTOR2):c.195T>C (p.Asn65=)	LAMTOR2, LOC129931594	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1650476	NM_014017.4(LAMTOR2):c.216C>T (p.Ile72=)	LAMTOR2, LOC129931594	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1494814	NM_014017.4(LAMTOR2):c.181A>C (p.Asn61His)	LAMTOR2, LOC129931594 (N61H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1419273	NM_014017.4(LAMTOR2):c.211T>C (p.Phe71Leu)	LAMTOR2, LOC129931594 (F71L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 750225	NM_014017.4(LAMTOR2):c.165C>T (p.Ala55=)	LAMTOR2, LOC129931594	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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