"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "FRAS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3379540	NM_025074.7(FRAS1):c.3974A>G (p.Gln1325Arg)	FRAS1 (Q1325R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 197043	NM_025074.7(FRAS1):c.5046C>G (p.Asp1682Glu)	FRAS1 (D1682E)	Single nucleotide variant (missense variant)	Fraser syndrome 1 +2 more	GConflicting classifications of pathogenicity
Select item 2682862	NM_025074.7(FRAS1):c.5557T>C (p.Ser1853Pro)	FRAS1 (S1853P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3379541	NM_025074.7(FRAS1):c.7292A>G (p.Asp2431Gly)	FRAS1 (D2431G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 198324	NM_025074.7(FRAS1):c.9364C>T (p.Arg3122Trp)	FRAS1 (R3122W)	Single nucleotide variant (missense variant)	Fraser syndrome 1 +4 more	GConflicting classifications of pathogenicity
Select item 547870	NM_025074.7(FRAS1):c.11717T>C (p.Ile3906Thr)	FRAS1 (I3906T)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity

ClinVar