"Color Diagnostics, LLC DBA Color Health"[submitter] AND "SDHAF2"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 463832	NM_017841.4(SDHAF2):c.6G>A (p.Ala2=)	SDHAF2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GLikely benign
Select item 2774506	NM_017841.4(SDHAF2):c.9_19del (p.Ser4fs)	SDHAF2 (S4fs)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely pathogenic
Select item 1451844	NM_017841.4(SDHAF2):c.28del (p.Ser10fs)	SDHAF2 (S10fs)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 384524	NM_017841.4(SDHAF2):c.165G>A (p.Trp55Ter)	SDHAF2 (W55*)	Single nucleotide variant (nonsense)	Hereditary pheochromocytoma-paraganglioma +4 more	GConflicting classifications of pathogenicity
Select item 1452374	NM_017841.4(SDHAF2):c.229_230del (p.Arg77fs)	SDHAF2 (R77fs)	Microsatellite (frameshift variant)	Paragangliomas 2 +1 more	GPathogenic/Likely pathogenic
Select item 700945	NM_017841.4(SDHAF2):c.269C>T (p.Ala90Val)	SDHAF2 (A90V)	Single nucleotide variant (missense variant)	Hereditary pheochromocytoma-paraganglioma +3 more	GBenign/Likely benign
Select item 823022	NM_017841.4(SDHAF2):c.315T>A (p.Tyr105Ter)	SDHAF2 (Y105*)	Single nucleotide variant (nonsense)	Paragangliomas 2 +3 more	GPathogenic/Likely pathogenic

ClinVar