"Ambry Genetics"[submitter] AND "LOC130058824"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2395240	NM_015527.4(TBC1D10B):c.80G>A (p.Gly27Asp)	LOC130058824, TBC1D10B (G27D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388722	NM_015527.4(TBC1D10B):c.77G>T (p.Arg26Leu)	LOC130058824, TBC1D10B (R26L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222180	NM_015527.4(TBC1D10B):c.76C>T (p.Arg26Trp)	LOC130058824, TBC1D10B (R26W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554857	NM_015527.4(TBC1D10B):c.70C>G (p.Pro24Ala)	LOC130058824, TBC1D10B (P24A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592695	NM_015527.4(TBC1D10B):c.49G>C (p.Ala17Pro)	LOC130058824, TBC1D10B (A17P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174412	NM_015527.4(TBC1D10B):c.44A>G (p.His15Arg)	LOC130058824, TBC1D10B (H15R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174411	NM_015527.4(TBC1D10B):c.34C>T (p.Pro12Ser)	LOC130058824, TBC1D10B (P12S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar