"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "TLE6"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1879408	NM_001143986.2(TLE6):c.585C>T (p.Ser195=)	TLE6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2498746	NM_001143986.2(TLE6):c.628C>T (p.Pro210Ser)	TLE6 (P210S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3026334	NM_001143986.2(TLE6):c.784G>A (p.Asp262Asn)	TLE6 (D139N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2648980	NM_001143986.2(TLE6):c.841C>A (p.Arg281=)	TLE6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1879409	NM_001143986.2(TLE6):c.901G>A (p.Val301Met)	TLE6 (V178M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2578815	NM_001143986.2(TLE6):c.997C>T (p.Pro333Ser)	TLE6 (P210S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2571025	NM_001143986.2(TLE6):c.1519G>A (p.Val507Ile)	TLE6 (V384I +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign

ClinVar