C5436668[trait identifier] AND "Johns Hopkins Genomics, Johns Hopkins - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2575227	NM_017654.4(SAMD9):c.4526A>G (p.Asn1509Ser)	SAMD9 (N1509S)	Single nucleotide variant (missense variant)	Monosomy 7 myelodysplasia and leukemia syndrome 2	GUncertain significance
Select item 2690903	NM_017654.4(SAMD9):c.1816A>G (p.Ile606Val)	SAMD9 (I606V)	Single nucleotide variant (missense variant)	Monosomy 7 myelodysplasia and leukemia syndrome 2	GUncertain significance