"Ambry Genetics"[submitter] AND "MB"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3124019	NM_005368.3(MB):c.425A>G (p.Asp142Gly)	MB (D87G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368811	NM_005368.3(MB):c.418C>T (p.Arg140Trp)	MB (R140W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124018	NM_005368.3(MB):c.407T>A (p.Leu136Gln)	MB (L136Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124017	NM_005368.3(MB):c.395T>A (p.Met132Lys)	MB (M132K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599774	NM_005368.3(MB):c.364G>A (p.Gly122Arg)	MB (G122R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329065	NM_005368.3(MB):c.354C>A (p.Ser118Arg)	MB (S118R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464200	NM_005368.3(MB):c.205G>A (p.Val69Met)	MB (V69M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480673	NM_005368.3(MB):c.44G>C (p.Trp15Ser)	MB (W15S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar