Related gene-specific medical variations for Gene (Select 54923) - ClinVar - NCBI

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Items: 14

	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 3193468	NM_181485.3(ZGPAT):c.1477G>T (p.Ala493Ser)	LIME1, ZGPAT (A493S +2 more)	Single nucleotide variant (5 prime UTR 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 2608537	NM_181485.3(ZGPAT):c.1465C>T (p.Arg489Trp)	LIME1, ZGPAT (R509W +2 more)	Single nucleotide variant (5 prime UTR variant +1 more)	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 2553560	NM_181485.3(ZGPAT):c.1478C>T (p.Ala493Val)	LIME1, ZGPAT (A513V +2 more)	Single nucleotide variant (5 prime UTR 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
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 2466530	NM_181485.3(ZGPAT):c.1466G>A (p.Arg489Gln)	LIME1, ZGPAT (R489Q +2 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2454410	NM_181485.3(ZGPAT):c.1402A>T (p.Ser468Cys)	LIME1, ZGPAT (S459C +2 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2336454	NM_181485.3(ZGPAT):c.1409C>T (p.Ala470Val)	LIME1, ZGPAT (A490V +2 more)	Single nucleotide variant (5 prime UTR 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 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 2276032	NM_181485.3(ZGPAT):c.1442C>T (p.Ala481Val)	LIME1, ZGPAT (A472V +2 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance