"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "FAT1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2682878	NM_005245.4(FAT1):c.11819C>T (p.Thr3940Ile)	FAT1 (T3940I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2294114	NM_005245.4(FAT1):c.11036A>G (p.Gln3679Arg)	FAT1, LOC126807254 (Q3679R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3379574	NM_005245.4(FAT1):c.10120A>G (p.Ile3374Val)	FAT1 (I3374V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2200070	NM_005245.4(FAT1):c.7769A>G (p.Asn2590Ser)	FAT1 (N2590S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3379575	NM_005245.4(FAT1):c.7366G>A (p.Ala2456Thr)	FAT1 (A2456T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2287151	NM_005245.4(FAT1):c.7118A>G (p.Asp2373Gly)	FAT1 (D2373G)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3379576	NM_005245.4(FAT1):c.6904G>A (p.Val2302Ile)	FAT1 (V2302I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 597999	NM_005245.4(FAT1):c.4516C>T (p.Arg1506Cys)	FAT1 (R1506C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar