"Ambry Genetics"[submitter] AND "CCNT1"[gene] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2207885	NM_001240.4(CCNT1):c.2125C>T (p.Arg709Trp)	CCNT1 (R639W +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493392	NM_001240.4(CCNT1):c.1994A>C (p.His665Pro)	CCNT1 (H600P +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2607890	NM_001240.4(CCNT1):c.1898G>A (p.Arg633His)	CCNT1 (R633H +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2343579	NM_001240.4(CCNT1):c.1889G>A (p.Cys630Tyr)	CCNT1 (C560Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140015	NM_001240.4(CCNT1):c.1847A>G (p.His616Arg)	CCNT1 (H331R +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2298604	NM_001240.4(CCNT1):c.1839G>T (p.Met613Ile)	CCNT1 (M548I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140014	NM_001240.4(CCNT1):c.1691C>T (p.Ser564Phe)	CCNT1 (S499F +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2410411	NM_001240.4(CCNT1):c.1655G>A (p.Ser552Asn)	CCNT1 (S487N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264604	NM_001240.4(CCNT1):c.1596A>T (p.Gln532His)	CCNT1 (Q467H +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3264605	NM_001240.4(CCNT1):c.1523A>T (p.Glu508Val)	CCNT1 (E223V +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3264603	NM_001240.4(CCNT1):c.1495A>G (p.Ser499Gly)	CCNT1 (S434G +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3264606	NM_001240.4(CCNT1):c.1481A>G (p.Asn494Ser)	CCNT1 (N429S +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3264601	NM_001240.4(CCNT1):c.1480A>G (p.Asn494Asp)	CCNT1 (N209D +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3140013	NM_001240.4(CCNT1):c.1448G>T (p.Arg483Leu)	CCNT1 (R198L +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2373122	NM_001240.4(CCNT1):c.1447C>T (p.Arg483Cys)	CCNT1 (R413C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2323657	NM_001240.4(CCNT1):c.1430C>T (p.Pro477Leu)	CCNT1 (P407L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343578	NM_001240.4(CCNT1):c.1409A>G (p.Asp470Gly)	CCNT1 (D185G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264602	NM_001240.4(CCNT1):c.1345C>T (p.Arg449Trp)	CCNT1 (R384W +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3140012	NM_001240.4(CCNT1):c.1316T>C (p.Met439Thr)	CCNT1 (M439T +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3140010	NM_001240.4(CCNT1):c.1307T>C (p.Ile436Thr)	CCNT1 (I151T +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3264607	NM_001240.4(CCNT1):c.1303G>A (p.Val435Ile)	CCNT1 (V150I +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2523835	NM_001240.4(CCNT1):c.1252T>C (p.Tyr418His)	CCNT1 (Y133H +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2401659	NM_001240.4(CCNT1):c.1181C>T (p.Ala394Val)	CCNT1 (A324V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317699	NM_001240.4(CCNT1):c.1180G>A (p.Ala394Thr)	CCNT1 (A329T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2587999	NM_001240.4(CCNT1):c.1147C>G (p.Pro383Ala)	CCNT1 (P313A +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3140009	NM_001240.4(CCNT1):c.1084C>G (p.His362Asp)	CCNT1 (H292D +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2339752	NM_001240.4(CCNT1):c.1067C>A (p.Ala356Glu)	CCNT1 (A356E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2305969	NM_001240.4(CCNT1):c.988C>G (p.Pro330Ala)	CCNT1 (P260A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543820	NM_001240.4(CCNT1):c.843G>C (p.Gln281His)	CCNT1 (Q211H +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2609541	NM_001240.4(CCNT1):c.818G>A (p.Gly273Glu)	CCNT1 (G273E +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2293689	NM_001240.4(CCNT1):c.800C>G (p.Thr267Arg)	CCNT1 (T267R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392319	NM_001240.4(CCNT1):c.212T>C (p.Met71Thr)	CCNT1 (M71T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337524	NM_001240.4(CCNT1):c.106T>C (p.Ser36Pro)	CCNT1, LOC130007793 (S36P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 33