"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "GBF1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2683123	NM_001377137.1(GBF1):c.684G>T (p.Lys228Asn)	GBF1 (K228N +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2630853	NM_001377137.1(GBF1):c.991C>T (p.Pro331Ser)	GBF1 (P331S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3379990	NM_001377137.1(GBF1):c.1408C>T (p.Arg470Ter)	GBF1 (R343* +4 more)	Single nucleotide variant (nonsense +2 more)	not provided	GUncertain significance
Select item 3379991	NM_001377137.1(GBF1):c.1973G>A (p.Gly658Glu)	GBF1 (G531E +7 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2683124	NM_001377137.1(GBF1):c.3677G>A (p.Arg1226His)	GBF1 (R1099H +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3379992	NM_001377137.1(GBF1):c.4414C>T (p.Arg1472Trp)	GBF1 (R1345W +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

ClinVar