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

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

Search results

Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3142226	NM_198489.3(CENATAC):c.25C>G (p.Leu9Val)	CENATAC, LOC121392945 (L9V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2595676	NM_198489.3(CENATAC):c.37A>G (p.Thr13Ala)	CENATAC, LOC121392945 (T13A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142232	NM_198489.3(CENATAC):c.52C>A (p.Arg18Ser)	CENATAC, LOC121392945 (R18S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142221	NM_198489.3(CENATAC):c.110T>C (p.Leu37Pro)	CENATAC, LOC121392945 (L37P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142222	NM_198489.3(CENATAC):c.151G>C (p.Ala51Pro)	CENATAC, LOC121392945 (A51P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142223	NM_198489.3(CENATAC):c.167A>G (p.Tyr56Cys)	CENATAC, LOC121392945 (Y56C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142224	NM_198489.3(CENATAC):c.172C>G (p.Pro58Ala)	CENATAC, LOC121392945 (P58A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142225	NM_198489.3(CENATAC):c.215A>T (p.Glu72Val)	CENATAC, LOC121392945 (E72V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470527	NM_198489.3(CENATAC):c.263G>A (p.Gly88Glu)	CENATAC, LOC121392945 (G88E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142227	NM_198489.3(CENATAC):c.308A>G (p.Asn103Ser)	CENATAC, LOC121392945 (N103S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142228	NM_198489.3(CENATAC):c.309C>G (p.Asn103Lys)	CENATAC, LOC121392945 (N103K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142229	NM_198489.3(CENATAC):c.422A>G (p.Glu141Gly)	CENATAC (E141G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142230	NM_198489.3(CENATAC):c.462G>C (p.Gln154His)	CENATAC (Q154H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142231	NM_198489.3(CENATAC):c.485G>A (p.Arg162Gln)	CENATAC (R162Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588293	NM_198489.3(CENATAC):c.530A>G (p.Asp177Gly)	CENATAC (D177G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469672	NM_198489.3(CENATAC):c.532C>A (p.Pro178Thr)	CENATAC (P178T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474524	NM_198489.3(CENATAC):c.601C>G (p.Gln201Glu)	CENATAC (Q201E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142233	NM_198489.3(CENATAC):c.613T>G (p.Leu205Val)	CENATAC (L205V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142234	NM_198489.3(CENATAC):c.674T>C (p.Ile225Thr)	CENATAC (I225T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2621418	NM_198489.3(CENATAC):c.724C>T (p.Pro242Ser)	CENATAC (P242S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142235	NM_198489.3(CENATAC):c.747A>T (p.Glu249Asp)	CENATAC (E249D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2561175	NM_198489.3(CENATAC):c.811A>G (p.Lys271Glu)	CENATAC (K271E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142236	NM_198489.3(CENATAC):c.840C>A (p.Asp280Glu)	CENATAC (D280E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142237	NM_198489.3(CENATAC):c.904C>T (p.Arg302Cys)	CENATAC (R302C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142238	NM_198489.3(CENATAC):c.961G>C (p.Ala321Pro)	CENATAC (A321P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142239	NM_198489.3(CENATAC):c.986C>T (p.Thr329Ile)	CENATAC (T329I)	Single nucleotide variant (missense 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: 26