"PreventionGenetics, part of Exact Sciences"[submitter] AND "RUNX1T1"[ - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3058834	NM_175634.3(RUNX1T1):c.1737G>A (p.Pro579=)	RUNX1T1	Single nucleotide variant (synonymous variant)	RUNX1T1-related disorder	GLikely benign
Select item 725597	NM_175634.3(RUNX1T1):c.1566G>A (p.Ala522=)	RUNX1T1	Single nucleotide variant (synonymous variant)	RUNX1T1-related disorder +1 more	GBenign/Likely benign
Select item 3041693	NM_175634.3(RUNX1T1):c.1473C>T (p.Ala491=)	RUNX1T1	Single nucleotide variant (synonymous variant)	RUNX1T1-related disorder	GLikely benign
Select item 3035332	NM_175634.3(RUNX1T1):c.1280-6dup	RUNX1T1	Duplication (intron variant)	RUNX1T1-related disorder	GLikely benign
Select item 785257	NM_175634.3(RUNX1T1):c.1165T>C (p.Leu389=)	RUNX1T1	Single nucleotide variant (synonymous variant)	RUNX1T1-related disorder +1 more	GBenign
Select item 784134	NM_175634.3(RUNX1T1):c.1077+7C>T	RUNX1T1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 3053818	NM_175634.3(RUNX1T1):c.840C>T (p.Asn280=)	RUNX1T1	Single nucleotide variant (synonymous variant)	RUNX1T1-related disorder	GBenign
Select item 710209	NM_175634.3(RUNX1T1):c.828C>T (p.Tyr276=)	RUNX1T1	Single nucleotide variant (synonymous variant)	RUNX1T1-related disorder +1 more	GBenign/Likely benign
Select item 3033200	NM_175634.3(RUNX1T1):c.597C>T (p.Cys199=)	RUNX1T1	Single nucleotide variant (synonymous variant)	RUNX1T1-related disorder	GLikely benign
Select item 719616	NM_175634.3(RUNX1T1):c.465A>G (p.Leu155=)	RUNX1T1	Single nucleotide variant (synonymous variant)	RUNX1T1-related disorder +1 more	GBenign/Likely benign
Select item 3045604	NM_175634.3(RUNX1T1):c.226+10C>T	RUNX1T1	Single nucleotide variant (intron variant)	RUNX1T1-related disorder	GLikely benign