"Ambry Genetics"[submitter] AND "TAL1"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3173662	NM_001290403.2(TAL1):c.929C>T (p.Pro310Leu)	TAL1 (P310L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343602	NM_001290403.2(TAL1):c.925G>T (p.Ala309Ser)	TAL1 (A309S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620399	NM_001290403.2(TAL1):c.849C>G (p.Asp283Glu)	TAL1 (D124E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374689	NM_001290403.2(TAL1):c.805G>A (p.Gly269Ser)	TAL1 (G110S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173661	NM_001290403.2(TAL1):c.800G>A (p.Gly267Asp)	TAL1 (G267D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326434	NM_001290403.2(TAL1):c.799G>A (p.Gly267Ser)	TAL1 (G267S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173660	NM_001290403.2(TAL1):c.533T>C (p.Ile178Thr)	TAL1 (I178T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373337	NM_001290403.2(TAL1):c.488C>T (p.Thr163Ile)	TAL1 (T163I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457179	NM_001290403.2(TAL1):c.395C>G (p.Pro132Arg)	TAL1 (P132R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363302	NM_001290403.2(TAL1):c.392C>T (p.Ala131Val)	TAL1 (A131V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397194	NM_001290403.2(TAL1):c.383C>A (p.Ala128Asp)	TAL1 (A128D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542637	NM_001290403.2(TAL1):c.340G>A (p.Gly114Ser)	TAL1 (G114S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350465	NM_001290403.2(TAL1):c.262G>A (p.Val88Met)	TAL1 (V88M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2274912	NM_001290403.2(TAL1):c.212C>T (p.Ala71Val)	TAL1 (A71V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483255	NM_001290403.2(TAL1):c.211G>C (p.Ala71Pro)	TAL1 (A71P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2309580	NM_001290403.2(TAL1):c.166G>T (p.Ala56Ser)	TAL1 (A56S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2282966	NM_001290403.2(TAL1):c.88C>G (p.His30Asp)	TAL1 (H30D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2376152	NM_001290403.2(TAL1):c.64G>A (p.Ala22Thr)	TAL1 (A22T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2351034	NM_001290403.2(TAL1):c.31C>T (p.Arg11Cys)	TAL1 (R11C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance