CALCOCO2[gene] and "single gene"[properties] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3262956	NM_005831.5(CALCOCO2):c.152G>A (p.Arg51His)	CALCOCO2 (R51H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295881	NM_005831.5(CALCOCO2):c.193A>G (p.Thr65Ala)	CALCOCO2 (T89A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322201	NM_005831.5(CALCOCO2):c.200G>A (p.Arg67His)	CALCOCO2 (R67H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535681	NM_005831.5(CALCOCO2):c.211A>G (p.Thr71Ala)	CALCOCO2 (T95A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2381544	NM_005831.5(CALCOCO2):c.349C>T (p.Arg117Trp)	CALCOCO2 (R45W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3136656	NM_005831.5(CALCOCO2):c.376C>T (p.Arg126Cys)	CALCOCO2 (R126C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531951	NM_005831.5(CALCOCO2):c.421G>A (p.Glu141Lys)	CALCOCO2 (E165K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2475887	NM_005831.5(CALCOCO2):c.491T>A (p.Ile164Asn)	CALCOCO2 (I188N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262955	NM_005831.5(CALCOCO2):c.507G>T (p.Gln169His)	CALCOCO2 (Q190H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3136657	NM_005831.5(CALCOCO2):c.524C>T (p.Ala175Val)	CALCOCO2 (A196V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602653	NM_005831.5(CALCOCO2):c.541C>A (p.Gln181Lys)	CALCOCO2 (Q202K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2356236	NM_005831.5(CALCOCO2):c.566G>A (p.Ser189Asn)	CALCOCO2 (S117N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485763	NM_005831.5(CALCOCO2):c.617A>C (p.Glu206Ala)	CALCOCO2 (E206A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3262954	NM_005831.5(CALCOCO2):c.649C>G (p.Gln217Glu)	CALCOCO2 (Q145E +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3262957	NM_005831.5(CALCOCO2):c.692A>G (p.Asp231Gly)	CALCOCO2 (D189G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213831	NM_005831.5(CALCOCO2):c.800A>G (p.His267Arg)	CALCOCO2 (H225R +4 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2330619	NM_005831.5(CALCOCO2):c.911T>C (p.Met304Thr)	CALCOCO2 (M232T +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3136658	NM_005831.5(CALCOCO2):c.935A>G (p.Lys312Arg)	CALCOCO2 (K270R +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2205689	NM_005831.5(CALCOCO2):c.952G>A (p.Glu318Lys)	CALCOCO2 (E342K +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3262953	NM_005831.5(CALCOCO2):c.968C>A (p.Ala323Asp)	CALCOCO2 (A251D +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331647	NM_005831.5(CALCOCO2):c.1043A>G (p.Tyr348Cys)	CALCOCO2 (Y276C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550400	NM_005831.5(CALCOCO2):c.1127A>G (p.Tyr376Cys)	CALCOCO2 (Y304C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541430	NM_005831.5(CALCOCO2):c.1169G>C (p.Ser390Thr)	CALCOCO2 (S318T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515959	NM_005831.5(CALCOCO2):c.1224C>A (p.His408Gln)	CALCOCO2 (H432Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590491	NM_005831.5(CALCOCO2):c.1262A>G (p.Asn421Ser)	CALCOCO2 (N442S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25