CCT8[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2242874	NM_006585.4(CCT8):c.1603C>T (p.Pro535Ser)	CCT8 (P462S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140210	NM_006585.4(CCT8):c.1428A>T (p.Lys476Asn)	CCT8 (K476N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554661	NM_006585.4(CCT8):c.1372G>A (p.Val458Ile)	CCT8 (V439I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140209	NM_006585.4(CCT8):c.1352C>T (p.Ala451Val)	CCT8 (A432V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469613	NM_006585.4(CCT8):c.1351G>A (p.Ala451Thr)	CCT8 (A400T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140208	NM_006585.4(CCT8):c.1340C>T (p.Ala447Val)	CCT8 (A396V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 769121	NM_006585.4(CCT8):c.1225G>A (p.Val409Ile)	CCT8 (V390I +3 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2228827	NM_006585.4(CCT8):c.1214A>T (p.Asp405Val)	CCT8 (D386V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540236	NM_006585.4(CCT8):c.1210A>G (p.Arg404Gly)	CCT8 (R331G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486129	NM_006585.4(CCT8):c.1127T>G (p.Val376Gly)	CCT8 (V357G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300747	NM_006585.4(CCT8):c.992C>T (p.Thr331Ile)	CCT8 (T280I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140216	NM_006585.4(CCT8):c.976A>G (p.Lys326Glu)	CCT8 (K275E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381612	NM_006585.4(CCT8):c.937G>A (p.Val313Met)	CCT8 (V240M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140214	NM_006585.4(CCT8):c.860G>T (p.Gly287Val)	CCT8 (G214V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140213	NM_006585.4(CCT8):c.565T>C (p.Ser189Pro)	CCT8 (S189P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596074	NM_006585.4(CCT8):c.545T>C (p.Leu182Pro)	CCT8 (L163P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261928	NM_006585.4(CCT8):c.474T>A (p.Asp158Glu)	CCT8 (D139E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140212	NM_006585.4(CCT8):c.470T>C (p.Ile157Thr)	CCT8 (I106T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346839	NM_006585.4(CCT8):c.442T>C (p.Cys148Arg)	CCT8 (C129R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229417	NM_006585.4(CCT8):c.302C>T (p.Thr101Ile)	CCT8 (T101I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386880	NM_006585.4(CCT8):c.211A>G (p.Thr71Ala)	CCT8 (T52A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349958	NM_006585.4(CCT8):c.200A>C (p.Asn67Thr)	CCT8 (N67T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2229462	NM_006585.4(CCT8):c.131G>A (p.Arg44His)	CCT8 (R25H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140207	NM_006585.4(CCT8):c.107G>T (p.Cys36Phe)	CCT8 (C17F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140215	NM_006585.4(CCT8):c.89A>T (p.Tyr30Phe)	CCT8 (Y30F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477569	NM_006585.4(CCT8):c.53G>A (p.Gly18Glu)	CCT8 (G18E)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3140211	NM_006585.4(CCT8):c.43C>T (p.Leu15Phe)	CCT8 (L15F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2323529	NM_006585.4(CCT8):c.34G>A (p.Ala12Thr)	CCT8 (A12T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2471904	NM_006585.4(CCT8):c.22G>C (p.Ala8Pro)	CCT8 (A8P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 29