"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC126861 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3031938	NM_006755.2(TALDO1):c.462-10C>T	LOC126861110, TALDO1	Single nucleotide variant (intron variant)	TALDO1-related disorder	GLikely benign
Select item 2166238	NM_006755.2(TALDO1):c.462-9G>A	LOC126861110, TALDO1	Single nucleotide variant (intron variant)	TALDO1-related disorder +1 more	GLikely benign
Select item 2156000	NM_006755.2(TALDO1):c.501G>A (p.Thr167=)	LOC126861110, TALDO1	Single nucleotide variant (synonymous variant)	TALDO1-related disorder +1 more	GLikely benign
Select item 1549483	NM_006755.2(TALDO1):c.638-5T>C	LOC126861110, TALDO1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 3040700	NM_006755.2(TALDO1):c.646_647del (p.Ser216fs)	LOC126861110, TALDO1 (S216fs)	Microsatellite (frameshift variant)	TALDO1-related disorder	GLikely pathogenic
Select item 3057204	NM_006755.2(TALDO1):c.651C>T (p.Val217=)	LOC126861110, TALDO1	Single nucleotide variant (synonymous variant)	TALDO1-related disorder	GLikely benign
Select item 3031477	NM_006755.2(TALDO1):c.656A>G (p.Lys219Arg)	LOC126861110, TALDO1 (K219R)	Single nucleotide variant (missense variant)	TALDO1-related disorder	GUncertain significance

ClinVar