"Ambry Genetics"[submitter] AND "NUB1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3202690	NM_001243351.2(NUB1):c.200C>A (p.Ala67Glu)	NUB1 (A67E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202691	NM_001243351.2(NUB1):c.422C>T (p.Thr141Ile)	NUB1 (T141I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3301333	NM_001243351.2(NUB1):c.509A>G (p.Gln170Arg)	NUB1 (Q170R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620931	NM_001243351.2(NUB1):c.712G>A (p.Gly238Arg)	NUB1 (G238R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202689	NM_001243351.2(NUB1):c.1495G>A (p.Val499Met)	NUB1, WDR86 (V485M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275665	NM_001243351.2(NUB1):c.1555G>T (p.Val519Phe)	NUB1, WDR86 (V519F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394683	NM_001243351.2(NUB1):c.1568C>T (p.Ala523Val)	NUB1, WDR86 (A508V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349084	NM_001243351.2(NUB1):c.1654C>T (p.Pro552Ser)	NUB1, WDR86 (P537S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar