"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "F13A1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1705952	NM_000129.4(F13A1):c.1503C>A (p.Tyr501Ter)	F13A1 (Y501*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1705953	NM_000129.4(F13A1):c.826C>T (p.Leu276Phe)	F13A1 (L276F)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 16537	NM_000129.4(F13A1):c.691-1G>A	F13A1	Single nucleotide variant (splice acceptor variant)	not provided +1 more	GPathogenic

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