"Ambry Genetics"[submitter] AND "MYEOV"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2327611	NM_001293291.2(MYEOV):c.107G>A (p.Arg36His)	MYEOV (R36H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2397295	NM_001293291.2(MYEOV):c.347A>G (p.Gln116Arg)	MYEOV (Q116R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251782	NM_001293291.2(MYEOV):c.611G>A (p.Arg204His)	MYEOV (R204H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251323	NM_001293291.2(MYEOV):c.808G>A (p.Gly270Arg)	MYEOV (G212R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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