CCT6B[gene] and "single gene"[properties] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2289382	NM_006584.4(CCT6B):c.1574G>C (p.Gly525Ala)	CCT6B (G488A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248441	NM_006584.4(CCT6B):c.1553T>C (p.Val518Ala)	CCT6B (V481A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215036	NM_006584.4(CCT6B):c.1543A>G (p.Ile515Val)	CCT6B (I478V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318202	NM_006584.4(CCT6B):c.1529T>C (p.Val510Ala)	CCT6B (V473A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615171	NM_006584.4(CCT6B):c.1348G>T (p.Val450Phe)	CCT6B (V405F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380445	NM_006584.4(CCT6B):c.1343C>T (p.Pro448Leu)	CCT6B (P403L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323479	NM_006584.4(CCT6B):c.1333C>T (p.Leu445Phe)	CCT6B (L408F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362308	NM_006584.4(CCT6B):c.1298C>A (p.Ala433Asp)	CCT6B (A396D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621795	NM_006584.4(CCT6B):c.1277A>G (p.Lys426Arg)	CCT6B (K426R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232522	NM_006584.4(CCT6B):c.1220T>C (p.Met407Thr)	CCT6B (M362T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616249	NM_006584.4(CCT6B):c.1192A>G (p.Ile398Val)	CCT6B (I398V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3140191	NM_006584.4(CCT6B):c.1055A>C (p.Glu352Ala)	CCT6B (E307A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620635	NM_006584.4(CCT6B):c.1028G>T (p.Cys343Phe)	CCT6B (C343F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483372	NM_006584.4(CCT6B):c.1015C>A (p.Leu339Ile)	CCT6B (L339I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508220	NM_006584.4(CCT6B):c.997G>A (p.Val333Met)	CCT6B (V296M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606735	NM_006584.4(CCT6B):c.955A>G (p.Arg319Gly)	CCT6B (R274G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621740	NM_006584.4(CCT6B):c.875T>C (p.Ile292Thr)	CCT6B (I255T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381368	NM_006584.4(CCT6B):c.784G>C (p.Ala262Pro)	CCT6B (A225P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246844	NM_006584.4(CCT6B):c.638A>G (p.Asp213Gly)	CCT6B (D168G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3250571	NM_006584.4(CCT6B):c.636G>A (p.Leu212=)	CCT6B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 778127	NM_006584.4(CCT6B):c.615-2A>G	CCT6B	Single nucleotide variant (splice acceptor variant +1 more)	not provided	GBenign
Select item 3140198	NM_006584.4(CCT6B):c.520G>A (p.Asp174Asn)	CCT6B (D129N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140197	NM_006584.4(CCT6B):c.343C>T (p.His115Tyr)	CCT6B (H70Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140196	NM_006584.4(CCT6B):c.321C>A (p.Asp107Glu)	CCT6B (D107E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531888	NM_006584.4(CCT6B):c.278C>T (p.Thr93Ile)	CCT6B (T93I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140193	NM_006584.4(CCT6B):c.253G>A (p.Asp85Asn)	CCT6B (D85N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491310	NM_006584.4(CCT6B):c.182A>G (p.Asn61Ser)	CCT6B (N61S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140192	NM_006584.4(CCT6B):c.10A>G (p.Ile4Val)	CCT6B (I4V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464781	NM_006584.4(CCT6B):c.5C>T (p.Ala2Val)	CCT6B (A2V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 29