"Ambry Genetics"[submitter] AND "LOC114803474"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3290748	NM_017806.4(LIME1):c.202C>T (p.Leu68Phe)	LIME1, LOC114803474 (L68F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325089	NM_017806.4(LIME1):c.262A>G (p.Ser88Gly)	LIME1, LOC114803474 (Q76R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520052	NM_017806.4(LIME1):c.280G>A (p.Ala94Thr)	LIME1, LOC114803474 (C82Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2566313	NM_017806.4(LIME1):c.353C>G (p.Ser118Cys)	LIME1, LOC114803474 (S118C)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3118886	NM_017806.4(LIME1):c.416C>T (p.Ala139Val)	LIME1, LOC114803474 (A139V)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2277663	NM_017806.4(LIME1):c.485C>T (p.Pro162Leu)	LIME1, LOC114803474 (P162L)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2544082	NM_017806.4(LIME1):c.520A>C (p.Lys174Gln)	LIME1, LOC114803474 (Q162P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar