Related gene-specific medical variations for Gene (Select 338657) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3265858	NM_198489.3(CENATAC):c.180C>G (p.His60Gln)	CENATAC, LOC121392945 (H60Q)	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 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 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 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 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 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 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 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 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 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 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 92038	NM_198489.3(CENATAC):c.815A>G (p.Gln272Arg)	CENATAC (Q272R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance