"Ambry Genetics"[submitter] AND "CCDC3"[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2343949	NM_031455.4(CCDC3):c.800A>C (p.Tyr267Ser)	CCDC3 (Y142S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519121	NM_031455.4(CCDC3):c.797C>G (p.Pro266Arg)	CCDC3 (P141R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478767	NM_031455.4(CCDC3):c.772A>C (p.Asn258His)	CCDC3 (N133H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617440	NM_031455.4(CCDC3):c.771C>G (p.Ile257Met)	CCDC3 (I257M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139090	NM_031455.4(CCDC3):c.749C>T (p.Ala250Val)	CCDC3 (A125V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221703	NM_031455.4(CCDC3):c.707G>T (p.Arg236Leu)	CCDC3 (R111L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139089	NM_031455.4(CCDC3):c.685C>T (p.Arg229Trp)	CCDC3 (R104W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264183	NM_031455.4(CCDC3):c.678G>T (p.Arg226Ser)	CCDC3 (R226S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273127	NM_031455.4(CCDC3):c.668A>T (p.Lys223Met)	CCDC3 (K223M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273126	NM_031455.4(CCDC3):c.667A>G (p.Lys223Glu)	CCDC3 (K223E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466725	NM_031455.4(CCDC3):c.637C>T (p.Arg213Cys)	CCDC3 (R213C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209625	NM_031455.4(CCDC3):c.516C>A (p.Phe172Leu)	CCDC3 (F47L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380565	NM_031455.4(CCDC3):c.509C>T (p.Ala170Val)	CCDC3 (A170V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3139087	NM_031455.4(CCDC3):c.349G>A (p.Asp117Asn)	CCDC3 (D117N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588731	NM_031455.4(CCDC3):c.341T>G (p.Val114Gly)	CCDC3 (V114G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244433	NM_031455.4(CCDC3):c.307G>T (p.Gly103Cys)	CCDC3 (G103C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139086	NM_031455.4(CCDC3):c.166C>T (p.Pro56Ser)	CCDC3 (P56S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525395	NM_031455.4(CCDC3):c.158C>T (p.Pro53Leu)	CCDC3 (P53L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2396005	NM_031455.4(CCDC3):c.98A>C (p.Glu33Ala)	CCDC3 (E33A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389647	NM_031455.4(CCDC3):c.86G>A (p.Arg29Lys)	CCDC3 (R29K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139088	NM_031455.4(CCDC3):c.56C>T (p.Ala19Val)	CCDC3 (A19V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353620	NM_031455.4(CCDC3):c.43C>G (p.Pro15Ala)	CCDC3 (P15A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314712	NM_031455.4(CCDC3):c.43C>A (p.Pro15Thr)	CCDC3 (P15T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362379	NM_031455.4(CCDC3):c.41G>A (p.Gly14Asp)	CCDC3 (G14D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 24