"Invitae"[submitter] AND "SLC25A10"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 712222	NM_012140.5(SLC25A10):c.372C>T (p.Asn124=)	SLC25A10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 730939	NM_012140.5(SLC25A10):c.458G>A (p.Arg153His)	SLC25A10 (R153H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 789234	NM_012140.5(SLC25A10):c.*28G>A	SLC25A10 (R270K)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 771770	NM_012140.5(SLC25A10):c.*38G>A	SLC25A10	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign/Likely benign
Select item 768922	NM_012140.5(SLC25A10):c.*111G>A	SLC25A10 (V298I)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 780471	NM_012140.5(SLC25A10):c.*236G>A	SLC25A10	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 2425656	NC_000017.10:g.(?_79618104)_(79894690_?)dup	ALYREF, ANAPC11 +17 more	Duplication	not provided	GUncertain significance
Select item 2424500	NC_000017.10:g.(?_79477716)_(80900339_?)dup	MAFG, MCRIP1 +52 more	Duplication	not provided	GUncertain significance

ClinVar