"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "MPIG6B"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3379641	NM_138272.3(MPIG6B):c.62C>G (p.Ala21Gly)	MPIG6B (A21G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3379642	NM_138272.3(MPIG6B):c.94A>C (p.Asn32His)	MPIG6B (N32H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3379643	NM_138272.3(MPIG6B):c.154G>A (p.Ala52Thr)	MPIG6B (A52T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 828136	NM_138272.3(MPIG6B):c.248G>A (p.Arg83His)	MPIG6B (R83H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1028384	NM_138272.3(MPIG6B):c.518C>A (p.Pro173Gln)	MPIG6B (P173Q)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 3379644	NM_138272.3(MPIG6B):c.542-13C>A	MPIG6B (P153T +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2634272	NM_138272.3(MPIG6B):c.542-9C>G	MPIG6B (P154R)	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GUncertain significance
Select item 988872	NM_138272.3(MPIG6B):c.621G>T (p.Pro207=)	MPIG6B (E170* +2 more)	Single nucleotide variant (nonsense +2 more)	not provided	GUncertain significance

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