"Ambry Genetics"[submitter] AND "LTA4H"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2350581	NM_000895.3(LTA4H):c.1811T>C (p.Val604Ala)	LTA4H (V569A +4 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2458890	NM_000895.3(LTA4H):c.1810G>T (p.Val604Leu)	LTA4H (V580L +4 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2353607	NM_000895.3(LTA4H):c.1760G>A (p.Arg587Gln)	LTA4H (R552Q +4 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2394190	NM_000895.3(LTA4H):c.1463A>G (p.Asn488Ser)	LTA4H (N464S +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2530434	NM_000895.3(LTA4H):c.1441G>A (p.Glu481Lys)	LTA4H (E446K +3 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2245506	NM_000895.3(LTA4H):c.1436C>T (p.Ala479Val)	LTA4H (A267V +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2610895	NM_000895.3(LTA4H):c.1435G>A (p.Ala479Thr)	LTA4H (A479T +3 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2538903	NM_000895.3(LTA4H):c.1277A>G (p.Lys426Arg)	LTA4H (K391R +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2369123	NM_000895.3(LTA4H):c.1241A>C (p.Lys414Thr)	LTA4H (K379T +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2318771	NM_000895.3(LTA4H):c.1100T>C (p.Val367Ala)	LTA4H (V367A +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2352185	NM_000895.3(LTA4H):c.1096C>G (p.Leu366Val)	LTA4H (L366V +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2267483	NM_000895.3(LTA4H):c.796T>G (p.Phe266Val)	LTA4H (F266V +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2340675	NM_000895.3(LTA4H):c.668C>G (p.Ser223Cys)	LTA4H (S188C +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2516306	NM_000895.3(LTA4H):c.524G>A (p.Arg175His)	LTA4H (R151H +1 more)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2286070	NM_000895.3(LTA4H):c.346C>T (p.Leu116Phe)	LTA4H (L116F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance