"PreventionGenetics, part of Exact Sciences"[submitter] AND "TAL1"[gen - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3056122	NM_001290403.2(TAL1):c.819C>T (p.Gly273=)	TAL1	Single nucleotide variant (synonymous variant)	TAL1-related disorder	GBenign
Select item 3050360	NM_001290403.2(TAL1):c.813A>C (p.Gly271=)	TAL1	Single nucleotide variant (synonymous variant)	TAL1-related disorder	GLikely benign
Select item 3033534	NM_001290403.2(TAL1):c.795T>G (p.Gly265=)	TAL1	Single nucleotide variant (synonymous variant)	TAL1-related disorder	GBenign
Select item 3034085	NM_001290403.2(TAL1):c.792T>G (p.Ala264=)	TAL1	Single nucleotide variant (synonymous variant)	TAL1-related disorder	GLikely benign
Select item 3045332	NM_001290403.2(TAL1):c.486C>G (p.Thr162=)	TAL1	Single nucleotide variant (synonymous variant)	TAL1-related disorder	GLikely benign
Select item 3038868	NM_001290403.2(TAL1):c.311C>T (p.Ala104Val)	TAL1 (A104V)	Single nucleotide variant (missense variant +1 more)	TAL1-related disorder	GLikely benign
Select item 3039271	NM_001290403.2(TAL1):c.310G>T (p.Ala104Ser)	TAL1 (A104S)	Single nucleotide variant (missense variant +1 more)	TAL1-related disorder	GLikely benign
Select item 3038998	NM_001290403.2(TAL1):c.184G>C (p.Gly62Arg)	TAL1 (G62R)	Single nucleotide variant (missense variant +1 more)	TAL1-related disorder	GLikely benign
Select item 3050612	NM_001290403.2(TAL1):c.80C>G (p.Ala27Gly)	TAL1 (A27G)	Single nucleotide variant (missense variant +1 more)	TAL1-related disorder	GLikely benign