TBC1D3C[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2346203	NM_001001418.6(TBC1D3C):c.1519G>A (p.Ala507Thr)	TBC1D3C (A507T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2378722	NM_001001418.6(TBC1D3C):c.1481A>G (p.Gln494Arg)	TBC1D3C (Q494R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348232	NM_001001418.6(TBC1D3C):c.1439T>C (p.Val480Ala)	TBC1D3C (V480A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409543	NM_001001418.6(TBC1D3C):c.1231C>T (p.Arg411Cys)	TBC1D3C (R411C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383911	NM_001001418.6(TBC1D3C):c.1195C>T (p.Arg399Trp)	TBC1D3C (R399W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213936	NM_001001418.6(TBC1D3C):c.1154G>C (p.Gly385Ala)	TBC1D3C (G385A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383866	NM_001001418.6(TBC1D3C):c.967C>T (p.Arg323Cys)	TBC1D3C (R323C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347755	NM_001001418.6(TBC1D3C):c.583G>A (p.Ala195Thr)	TBC1D3C (A195T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366961	NM_001001418.6(TBC1D3C):c.350= (p.Thr117=)	TBC1D3C	Variation (no sequence alteration)	not specified	GLikely benign
Select item 2344588	NM_001001418.6(TBC1D3C):c.97G>A (p.Asp33Asn)	TBC1D3C (D33N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance