CCDC51[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3139190	NM_001256964.2(CCDC51):c.416G>A (p.Arg139His)	CCDC51 (R139H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139189	NM_001256964.2(CCDC51):c.406C>T (p.Arg136Cys)	CCDC51 (R136C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139188	NM_001256964.2(CCDC51):c.392A>G (p.Lys131Arg)	CCDC51 (K22R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139187	NM_001256964.2(CCDC51):c.340G>C (p.Gly114Arg)	CCDC51 (G114R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139186	NM_001256964.2(CCDC51):c.334G>T (p.Ala112Ser)	CCDC51 (A3S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534823	NM_001256964.2(CCDC51):c.272G>A (p.Gly91Glu)	CCDC51 (G91E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473528	NM_001256964.2(CCDC51):c.176G>A (p.Arg59His)	CCDC51 (R59H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525714	NM_001256964.2(CCDC51):c.142A>G (p.Arg48Gly)	CCDC51 (R48G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 784002	NM_001256964.2(CCDC51):c.132C>T (p.Pro44=)	CCDC51	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2570293	NM_001256964.2(CCDC51):c.88C>T (p.Leu30Phe)	CCDC51 (L30F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139195	NM_001256964.2(CCDC51):c.65G>A (p.Arg22Gln)	CCDC51 (R22Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139194	NM_001256964.2(CCDC51):c.64C>T (p.Arg22Trp)	CCDC51 (R22W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508531	NM_001256964.2(CCDC51):c.55G>A (p.Val19Ile)	CCDC51 (V19I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign