"Ambry Genetics"[submitter] AND "TLE5"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3177828	NM_001130.6(TLE5):c.517G>A (p.Ala173Thr)	TLE5 (A172T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177827	NM_001130.6(TLE5):c.439G>A (p.Val147Met)	TLE5 (V147M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177826	NM_001130.6(TLE5):c.199A>G (p.Met67Val)	TLE5 (M67V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326302	NM_001130.6(TLE5):c.126C>T (p.Ser42=)	TLE5	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3177825	NM_198969.1(TLE5):c.201G>C (p.Trp67Cys)	TLE5 (W67C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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