"Ambry Genetics"[submitter] AND "CCNE1"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3264547	NM_001238.4(CCNE1):c.14G>T (p.Arg5Leu)	CCNE1 (R5L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264548	NM_001238.4(CCNE1):c.22C>T (p.Arg8Trp)	CCNE1 (R8W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301563	NM_001238.4(CCNE1):c.109G>C (p.Val37Leu)	CCNE1 (V37L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247773	NM_001238.4(CCNE1):c.112T>C (p.Phe38Leu)	CCNE1 (F23L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352448	NM_001238.4(CCNE1):c.125C>A (p.Pro42Gln)	CCNE1 (P27Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339663	NM_001238.4(CCNE1):c.232C>A (p.Pro78Thr)	CCNE1 (P78T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139916	NM_001238.4(CCNE1):c.245A>G (p.Asp82Gly)	CCNE1 (D82G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139917	NM_001238.4(CCNE1):c.247G>C (p.Asp83His)	CCNE1 (D68H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250582	NM_001238.4(CCNE1):c.319G>A (p.Val107Ile)	CCNE1 (V92I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139918	NM_001238.4(CCNE1):c.332C>G (p.Ala111Gly)	CCNE1 (A111G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139919	NM_001238.4(CCNE1):c.533C>T (p.Ala178Val)	CCNE1 (A163V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2610811	NM_001238.4(CCNE1):c.700A>G (p.Met234Val)	CCNE1 (M185V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308338	NM_001238.4(CCNE1):c.787C>T (p.His263Tyr)	CCNE1 (H248Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3139920	NM_001238.4(CCNE1):c.803C>T (p.Pro268Leu)	CCNE1 (P219L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623306	NM_001238.4(CCNE1):c.892A>G (p.Ile298Val)	CCNE1 (I253V +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3264549	NM_001238.4(CCNE1):c.972A>G (p.Ile324Met)	CCNE1 (I279M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345619	NM_001238.4(CCNE1):c.1048A>G (p.Arg350Gly)	CCNE1 (R305G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215831	NM_001238.4(CCNE1):c.1078A>G (p.Ile360Val)	CCNE1 (I311V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517588	NM_001238.4(CCNE1):c.1198G>A (p.Gly400Ser)	CCNE1 (G385S +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2623370	NM_001238.4(CCNE1):c.1216G>A (p.Gly406Arg)	CCNE1 (G357R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 20