Related gene-specific medical variations for Gene (Select 892) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3139895	NM_005190.4(CCNC):c.766A>C (p.Lys256Gln)	CCNC, TSTD3 (K171Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139894	NM_005190.4(CCNC):c.627G>T (p.Gln209His)	CCNC, TSTD3 (Q209H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139893	NM_005190.4(CCNC):c.365A>T (p.Tyr122Phe)	CCNC, TSTD3 (Y37F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139892	NM_005190.4(CCNC):c.343G>A (p.Val115Ile)	CCNC, TSTD3 (V30I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139891	NM_005190.4(CCNC):c.226T>G (p.Tyr76Asp)	CCNC, TSTD3 (Y76D)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3139890	NM_005190.4(CCNC):c.218A>G (p.Tyr73Cys)	CCNC, TSTD3 (Y73C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2238024	NM_005190.4(CCNC):c.754A>G (p.Thr252Ala)	CCNC, TSTD3 (T167A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 805963	NM_005190.4(CCNC):c.346+77dup	TSTD3, CCNC	Duplication (intron variant)	CIC-DUX Sarcoma	Gnot provided

ClinVar