CUL4A[gene] and "single gene"[properties] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2454700	NM_001008895.4(CUL4A):c.359C>T (p.Pro120Leu)	CUL4A (P120L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597104	NM_001008895.4(CUL4A):c.446T>A (p.Ile149Asn)	CUL4A (I4N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399053	NM_001008895.4(CUL4A):c.539C>T (p.Thr180Ile)	CUL4A (T180I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297845	NM_001008895.4(CUL4A):c.562G>A (p.Val188Ile)	CUL4A (V188I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383870	NM_001008895.4(CUL4A):c.566A>G (p.Gln189Arg)	CUL4A (Q189R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398910	NM_001008895.4(CUL4A):c.616G>A (p.Gly206Ser)	CUL4A (G206S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334563	NM_001008895.4(CUL4A):c.710A>G (p.Glu237Gly)	CUL4A (E137G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078957	NM_001008895.4(CUL4A):c.841A>G (p.Ser281Gly)	CUL4A (S181G +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3025547	NM_001008895.4(CUL4A):c.1037C>G (p.Thr346Ser)	CUL4A (T201S +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2368306	NM_001008895.4(CUL4A):c.1057A>G (p.Ile353Val)	CUL4A (I253V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293858	NM_001008895.4(CUL4A):c.1545G>T (p.Gln515His)	CUL4A (Q415H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078953	NM_001008895.4(CUL4A):c.1561A>G (p.Ile521Val)	CUL4A (I421V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356936	NM_001008895.4(CUL4A):c.1610C>T (p.Thr537Met)	CUL4A (T437M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078954	NM_001008895.4(CUL4A):c.1844T>C (p.Met615Thr)	CUL4A (M515T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance