"Ambry Genetics"[submitter] AND "CCNJ"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3139952	NM_001134375.2(CCNJ):c.94G>A (p.Gly32Ser)	CCNJ, ENTPD1-AS1 (G32S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239221	NM_001134375.2(CCNJ):c.386A>G (p.His129Arg)	CCNJ, ENTPD1-AS1 (H129R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519420	NM_001134375.2(CCNJ):c.473C>G (p.Ala158Gly)	CCNJ, ENTPD1-AS1 (A158G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387662	NM_001134375.2(CCNJ):c.653G>A (p.Arg218His)	CCNJ, ENTPD1-AS1 (R206H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466759	NM_001134375.2(CCNJ):c.685C>T (p.Arg229Cys)	CCNJ, ENTPD1-AS1 (R229C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242475	NM_001134375.2(CCNJ):c.695C>T (p.Ala232Val)	CCNJ, ENTPD1-AS1 (A232V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139950	NM_001134375.2(CCNJ):c.752A>T (p.Asn251Ile)	CCNJ, ENTPD1-AS1 (N239I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371023	NM_001134375.2(CCNJ):c.806A>C (p.Gln269Pro)	CCNJ, ENTPD1-AS1 (Q257P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517868	NM_001134375.2(CCNJ):c.841C>T (p.Arg281Trp)	CCNJ, ENTPD1-AS1 (R270W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139951	NM_001134375.2(CCNJ):c.917C>T (p.Ser306Leu)	CCNJ, ENTPD1-AS1 (S295L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463092	NM_001134375.2(CCNJ):c.996C>G (p.Phe332Leu)	CCNJ, ENTPD1-AS1 (F320L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231875	NM_001134375.2(CCNJ):c.1004G>A (p.Ser335Asn)	CCNJ, ENTPD1-AS1 (S335N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491309	NM_001134375.2(CCNJ):c.1016T>C (p.Leu339Pro)	CCNJ, ENTPD1-AS1 (L328P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance