"Ambry Genetics"[submitter] AND "CCNL2"[gene] - ClinVar

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Items: 46

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2366113	NM_030937.6(CCNL2):c.1517G>A (p.Arg506His)	CCNL2 (R284H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2470728	NM_030937.6(CCNL2):c.1508G>A (p.Arg503His)	CCNL2 (R372H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2375377	NM_030937.6(CCNL2):c.1489C>T (p.Arg497Cys)	CCNL2 (R366C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139978	NM_030937.6(CCNL2):c.1462C>A (p.His488Asn)	CCNL2 (H488N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2412399	NM_030937.6(CCNL2):c.1421G>A (p.Arg474Gln)	CCNL2 (R474Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508563	NM_030937.6(CCNL2):c.1420C>T (p.Arg474Trp)	CCNL2 (R343W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2228246	NM_030937.6(CCNL2):c.1409G>A (p.Arg470Gln)	CCNL2 (R248Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269097	NM_030937.6(CCNL2):c.1388G>A (p.Ser463Asn)	CCNL2 (S241N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2272187	NM_030937.6(CCNL2):c.1339C>T (p.Arg447Trp)	CCNL2 (R225W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507889	NM_030937.6(CCNL2):c.1306G>A (p.Ala436Thr)	CCNL2 (A436T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264592	NM_030937.6(CCNL2):c.1297C>G (p.Pro433Ala)	CCNL2 (P302A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139975	NM_030937.6(CCNL2):c.1208G>T (p.Arg403Met)	CCNL2 (R181M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557674	NM_030937.6(CCNL2):c.1196C>T (p.Ala399Val)	CCNL2 (A177V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334450	NM_030937.6(CCNL2):c.1142G>A (p.Arg381Gln)	CCNL2 (R250Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2403571	NM_030937.6(CCNL2):c.1130G>A (p.Gly377Glu)	CCNL2 (G246E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379903	NM_030937.6(CCNL2):c.1111G>A (p.Val371Met)	CCNL2 (V149M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2606851	NM_030937.6(CCNL2):c.1097A>G (p.Lys366Arg)	CCNL2 (K366R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264590	NM_030937.6(CCNL2):c.1085C>G (p.Ala362Gly)	CCNL2 (A140G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139974	NM_030937.6(CCNL2):c.1076T>C (p.Leu359Pro)	CCNL2 (L228P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530932	NM_030937.6(CCNL2):c.1039C>A (p.Pro347Thr)	CCNL2 (P125T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139983	NM_030937.6(CCNL2):c.998C>G (p.Pro333Arg)	CCNL2 (P202R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139982	NM_030937.6(CCNL2):c.959C>T (p.Thr320Ile)	CCNL2 (T189I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366884	NM_030937.6(CCNL2):c.937C>T (p.Arg313Trp)	CCNL2 (R313W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2562852	NM_030937.6(CCNL2):c.929C>T (p.Ala310Val)	CCNL2 (A310V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2309337	NM_030937.6(CCNL2):c.917A>C (p.Glu306Ala)	CCNL2 (E84A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139981	NM_030937.6(CCNL2):c.896A>T (p.Glu299Val)	CCNL2 (E168V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2246112	NM_030937.6(CCNL2):c.857G>A (p.Arg286Gln)	CCNL2 (R286Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139980	NM_030937.6(CCNL2):c.836A>C (p.Lys279Thr)	CCNL2 (K148T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264591	NM_030937.6(CCNL2):c.827T>C (p.Ile276Thr)	CCNL2 (I276T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2260891	NM_030937.6(CCNL2):c.798T>G (p.Phe266Leu)	CCNL2 (F266L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509782	NM_030937.6(CCNL2):c.782A>G (p.His261Arg)	CCNL2 (H39R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608089	NM_030937.6(CCNL2):c.754C>A (p.Leu252Met)	CCNL2 (L121M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2521733	NM_030937.6(CCNL2):c.545G>A (p.Arg182Gln)	CCNL2 (R182Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2306205	NM_030937.6(CCNL2):c.481G>A (p.Val161Met)	CCNL2 (V161M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2483018	NM_030937.6(CCNL2):c.386A>C (p.His129Pro)	CCNL2 (H129P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2333910	NM_030937.6(CCNL2):c.361G>C (p.Glu121Gln)	CCNL2 (E121Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2408956	NM_030937.6(CCNL2):c.211A>G (p.Thr71Ala)	CCNL2, LOC129929121 (T71A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3139977	NM_030937.6(CCNL2):c.130G>A (p.Gly44Arg)	CCNL2, LOC129929121 (G44R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3139976	NM_030937.6(CCNL2):c.122T>A (p.Leu41Gln)	CCNL2, LOC129929121 (L41Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3139979	NM_030937.6(CCNL2):c.76G>T (p.Gly26Trp)	CCNL2 (G26W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2205256	NM_030937.6(CCNL2):c.64G>T (p.Ala22Ser)	CCNL2 (A22S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2616165	NM_030937.6(CCNL2):c.52G>A (p.Ala18Thr)	CCNL2 (A18T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2249778	NM_030937.6(CCNL2):c.37T>G (p.Ser13Ala)	CCNL2 (S13A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3264588	NM_030937.6(CCNL2):c.28G>A (p.Ala10Thr)	CCNL2 (A10T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2402664	NM_030937.6(CCNL2):c.22G>C (p.Ala8Pro)	CCNL2 (A8P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3264587	NM_030937.6(CCNL2):c.20C>A (p.Ala7Glu)	CCNL2 (A7E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 46