DCAF16[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2251572	NM_017741.4(DCAF16):c.593C>T (p.Thr198Ile)	DCAF16 (T198I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080283	NM_017741.4(DCAF16):c.589A>G (p.Thr197Ala)	DCAF16 (T197A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270975	NM_017741.4(DCAF16):c.581C>T (p.Pro194Leu)	DCAF16 (P194L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290977	NM_017741.4(DCAF16):c.478A>C (p.Thr160Pro)	DCAF16 (T160P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080281	NM_017741.4(DCAF16):c.430G>A (p.Ala144Thr)	DCAF16 (A144T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318314	NM_017741.4(DCAF16):c.383T>C (p.Leu128Pro)	DCAF16 (L128P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460831	NM_017741.4(DCAF16):c.362T>A (p.Val121Asp)	DCAF16 (V121D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080280	NM_017741.4(DCAF16):c.337T>C (p.Trp113Arg)	DCAF16 (W113R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270974	NM_017741.4(DCAF16):c.288A>C (p.Arg96Ser)	DCAF16 (R96S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387014	NM_017741.4(DCAF16):c.278T>C (p.Ile93Thr)	DCAF16 (I93T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607154	NM_017741.4(DCAF16):c.277A>G (p.Ile93Val)	DCAF16 (I93V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303024	NM_017741.4(DCAF16):c.148G>A (p.Glu50Lys)	DCAF16 (E50K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555134	NM_017741.4(DCAF16):c.140C>T (p.Ser47Leu)	DCAF16 (S47L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368326	NM_017741.4(DCAF16):c.112G>A (p.Glu38Lys)	DCAF16 (E38K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080284	NM_017741.4(DCAF16):c.91G>A (p.Glu31Lys)	DCAF16 (E31K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080282	NM_017741.4(DCAF16):c.48T>G (p.Ser16Arg)	DCAF16 (S16R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080277	NM_017741.4(DCAF16):c.26A>T (p.Asp9Val)	DCAF16 (D9V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance