"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "SLC25A1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 159909	NM_005984.5(SLC25A1):c.894T>C (p.Asp298=)	SLC25A1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1462936	NM_005984.5(SLC25A1):c.787G>A (p.Gly263Ser)	SLC25A1 (G160S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 559378	NM_005984.5(SLC25A1):c.711A>T (p.Gly237=)	SLC25A1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3380688	NM_005984.5(SLC25A1):c.693C>T (p.Gly231=)	SLC25A1	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 159908	NM_005984.5(SLC25A1):c.279T>C (p.Gly93=)	SLC25A1	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GBenign/Likely benign
Select item 1710697	NM_005984.5(SLC25A1):c.18_24dup (p.Ala9fs)	SLC25A1 (A9fs)	Microsatellite (frameshift variant +1 more)	not provided	GPathogenic

ClinVar