"Ambry Genetics"[submitter] AND "TLE4"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2299235	NM_007005.6(TLE4):c.57G>T (p.Gln19His)	TLE4 (Q17H +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3326298	NM_007005.6(TLE4):c.490G>A (p.Gly164Ser)	TLE4 (G137S +13 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2536663	NM_007005.6(TLE4):c.527T>A (p.Leu176Gln)	TLE4 (L150Q +13 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2551339	NM_007005.6(TLE4):c.772G>A (p.Val258Ile)	TLE4 (V137I +13 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2329712	NM_007005.6(TLE4):c.800G>A (p.Arg267Gln)	TLE4 (R244Q +12 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3177824	NM_007005.6(TLE4):c.847C>T (p.Arg283Cys)	TLE4 (R162C +12 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2364569	NM_007005.6(TLE4):c.986G>A (p.Arg329Gln)	TLE4 (R260Q +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3326301	NM_007005.6(TLE4):c.988A>C (p.Thr330Pro)	TLE4 (T252P +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2610522	NM_007005.6(TLE4):c.1037T>C (p.Val346Ala)	TLE4 (V325A +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517726	NM_007005.6(TLE4):c.1090A>G (p.Met364Val)	TLE4 (M243V +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2313135	NM_007005.6(TLE4):c.1105C>G (p.Pro369Ala)	TLE4 (P275A +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339697	NM_007005.6(TLE4):c.1174G>A (p.Ala392Thr)	TLE4 (A271T +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2475331	NM_007005.6(TLE4):c.1213G>A (p.Ala405Thr)	TLE4 (A327T +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345539	NM_007005.6(TLE4):c.1318A>G (p.Thr440Ala)	TLE4 (T362A +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177823	NM_007005.6(TLE4):c.1430A>G (p.His477Arg)	TLE4 (H399R +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517554	NM_007005.6(TLE4):c.1693C>T (p.Pro565Ser)	TLE4 (P541S +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3326299	NM_007005.6(TLE4):c.1787G>T (p.Cys596Phe)	TLE4 (C502F +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299570	NM_007005.6(TLE4):c.1804G>A (p.Ala602Thr)	TLE4 (A481T +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3326300	NM_007005.6(TLE4):c.2074C>G (p.Pro692Ala)	TLE4 (P598A +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance