"Ambry Genetics"[submitter] AND "CUL5"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2517962	NM_003478.6(CUL5):c.13A>C (p.Asn5His)	CUL5, LOC130006694 (N5H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078964	NM_003478.6(CUL5):c.71C>T (p.Pro24Leu)	CUL5 (P24L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205034	NM_003478.6(CUL5):c.213G>T (p.Glu71Asp)	CUL5 (E71D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270319	NM_003478.6(CUL5):c.511G>A (p.Ala171Thr)	CUL5 (A171T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355640	NM_003478.6(CUL5):c.758G>A (p.Arg253Gln)	CUL5 (R253Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078965	NM_003478.6(CUL5):c.772G>A (p.Val258Ile)	CUL5 (V258I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303443	NM_003478.6(CUL5):c.907G>C (p.Val303Leu)	CUL5 (V303L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270320	NM_003478.6(CUL5):c.970G>A (p.Ala324Thr)	CUL5 (A324T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523382	NM_003478.6(CUL5):c.1161A>T (p.Leu387Phe)	CUL5 (L387F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589806	NM_003478.6(CUL5):c.1179G>A (p.Gly393=)	CUL5	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2279787	NM_003478.6(CUL5):c.1603G>T (p.Ala535Ser)	CUL5 (A535S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454649	NM_003478.6(CUL5):c.1973A>G (p.Lys658Arg)	CUL5 (K658R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078962	NM_003478.6(CUL5):c.2038G>A (p.Val680Ile)	CUL5 (V680I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078963	NM_003478.6(CUL5):c.2099G>A (p.Arg700Lys)	CUL5 (R700K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance