"Ambry Genetics"[submitter] AND "MIGA2"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2211124	NM_001329990.2(MIGA2):c.26C>T (p.Thr9Met)	MIGA2 (T9M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2211675	NM_001329990.2(MIGA2):c.205C>T (p.Arg69Trp)	MIGA2 (R133W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126466	NM_001329990.2(MIGA2):c.727C>T (p.Arg243Cys)	LOC126860773, MIGA2 (R243C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2367779	NM_001329990.2(MIGA2):c.842C>T (p.Ala281Val)	MIGA2 (A281V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222513	NM_001329990.2(MIGA2):c.859C>G (p.Leu287Val)	MIGA2 (L351V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2371405	NM_001329990.2(MIGA2):c.1321G>A (p.Ala441Thr)	MIGA2 (A441T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242927	NM_001329990.2(MIGA2):c.1457T>C (p.Met486Thr)	MIGA2 (M486T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2255635	NM_001329990.2(MIGA2):c.1675C>T (p.Arg559Cys)	MIGA2 (R559C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance