"Ambry Genetics"[submitter] AND "LOC129998720"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2611514	NM_012301.4(MAGI2):c.4154C>T (p.Ala1385Val)	LOC129998720, MAGI2 (A1385V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608585	NM_012301.4(MAGI2):c.4150G>T (p.Gly1384Trp)	LOC129998720, MAGI2 (G1384W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602030	NM_012301.4(MAGI2):c.4148C>T (p.Pro1383Leu)	LOC129998720, MAGI2 (P1383L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319772	NM_012301.4(MAGI2):c.4115C>T (p.Ala1372Val)	LOC129998720, MAGI2 (A1372V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 195685	NM_012301.4(MAGI2):c.4109G>C (p.Arg1370Pro)	LOC129998720, MAGI2 (R1370P +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 2255634	NM_012301.4(MAGI2):c.4088C>A (p.Ala1363Glu)	LOC129998720, MAGI2 (A1363E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246702	NM_012301.4(MAGI2):c.4055T>G (p.Leu1352Arg)	LOC129998720, MAGI2 (L1352R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 594574	NM_012301.4(MAGI2):c.4001G>T (p.Gly1334Val)	LOC129998720, MAGI2 (G1334V +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance