"PreventionGenetics, part of Exact Sciences"[submitter] AND "MEIS2"[ge - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2645154	NM_170675.5(MEIS2):c.1262A>G (p.His421Arg)	MEIS2 (H414R +1 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GBenign/Likely benign
Select item 2630216	NM_170675.5(MEIS2):c.855A>G (p.Lys285=)	MEIS2	Single nucleotide variant (synonymous variant +1 more)	MEIS2-related disorder	GUncertain significance
Select item 3046663	NM_170675.5(MEIS2):c.813T>C (p.Asp271=)	MEIS2	Single nucleotide variant (synonymous variant +1 more)	MEIS2-related disorder	GLikely benign
Select item 705193	NM_170675.5(MEIS2):c.810G>A (p.Pro270=)	MEIS2	Single nucleotide variant (synonymous variant +1 more)	MEIS2-related disorder +1 more	GLikely benign
Select item 532737	NM_170675.5(MEIS2):c.732C>T (p.Ser244=)	MEIS2	Single nucleotide variant (synonymous variant +1 more)	MEIS2-related disorder +1 more	GBenign
Select item 532739	NM_170675.5(MEIS2):c.507T>C (p.Asp169=)	MEIS2	Single nucleotide variant (synonymous variant +1 more)	MEIS2-related disorder +1 more	GBenign
Select item 532738	NM_170675.5(MEIS2):c.471T>C (p.His157=)	MEIS2	Single nucleotide variant (synonymous variant +1 more)	MEIS2-related disorder +2 more	GLikely benign
Select item 3029404	NM_170675.5(MEIS2):c.412T>C (p.Ser138Pro)	MEIS2 (S125P +2 more)	Single nucleotide variant (missense variant +1 more)	MEIS2-related disorder	GUncertain significance
Select item 3032205	NM_170675.5(MEIS2):c.388-1G>A	MEIS2	Single nucleotide variant (splice acceptor variant)	MEIS2-related disorder	GLikely pathogenic
Select item 3058104	NM_170675.5(MEIS2):c.223C>A (p.Arg75=)	MEIS2	Single nucleotide variant (synonymous variant +2 more)	MEIS2-related disorder	GLikely benign
Select item 3049240	NM_170675.5(MEIS2):c.153C>T (p.Tyr51=)	MEIS2	Single nucleotide variant (synonymous variant +2 more)	MEIS2-related disorder	GLikely benign
Select item 2632334	NM_170675.5(MEIS2):c.15C>G (p.Tyr5Ter)	MEIS2 (Y5*)	Single nucleotide variant (nonsense +2 more)	MEIS2-related disorder	GUncertain significance