Related gene-specific medical variations for Gene (Select 79364) - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3260211	NM_025112.5(ZXDC):c.478G>A (p.Ala160Thr)	LOC129937463, ZXDC (A160T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3260208	NM_025112.5(ZXDC):c.124C>A (p.Leu42Met)	LOC129937464, ZXDC (L42M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3260207	NM_025112.5(ZXDC):c.167G>T (p.Gly56Val)	LOC129937464, ZXDC (G56V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3260206	NM_025112.5(ZXDC):c.65G>A (p.Gly22Asp)	ZXDC, LOC129937464 (G22D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3199700	NM_025112.5(ZXDC):c.53G>A (p.Gly18Asp)	LOC129937464, ZXDC (G18D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3199698	NM_025112.5(ZXDC):c.515C>T (p.Thr172Met)	LOC129937463, ZXDC (T172M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3199697	NM_025112.5(ZXDC):c.497A>T (p.Gln166Leu)	LOC129937463, ZXDC (Q166L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3199696	NM_025112.5(ZXDC):c.362C>T (p.Pro121Leu)	LOC129937463, ZXDC (P121L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3199695	NM_025112.5(ZXDC):c.305T>A (p.Val102Asp)	LOC129937463, ZXDC (V102D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3199688	NM_025112.5(ZXDC):c.203A>T (p.Asp68Val)	LOC129937464, ZXDC (D68V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3199687	NM_025112.5(ZXDC):c.202G>T (p.Asp68Tyr)	LOC129937464, ZXDC (D68Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3199678	NM_025112.5(ZXDC):c.14C>T (p.Ala5Val)	LOC129937464, ZXDC (A5V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608390	NM_025112.5(ZXDC):c.11C>T (p.Pro4Leu)	LOC129937464, ZXDC (P4L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544366	NM_025112.5(ZXDC):c.478G>T (p.Ala160Ser)	LOC129937463, ZXDC (A160S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528213	NM_025112.5(ZXDC):c.188C>T (p.Pro63Leu)	LOC129937464, ZXDC (P63L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511235	NM_025112.5(ZXDC):c.112C>T (p.Arg38Cys)	LOC129937464, ZXDC (R38C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491013	NM_025112.5(ZXDC):c.77G>A (p.Arg26Gln)	LOC129937464, ZXDC (R26Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2478811	NM_025112.5(ZXDC):c.539C>G (p.Pro180Arg)	LOC129937463, ZXDC (P180R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398492	NM_025112.5(ZXDC):c.62C>T (p.Pro21Leu)	LOC129937464, ZXDC (P21L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349492	NM_025112.5(ZXDC):c.316A>G (p.Ser106Gly)	LOC129937463, ZXDC (S106G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321708	NM_025112.5(ZXDC):c.401A>G (p.Gln134Arg)	LOC129937463, ZXDC (Q134R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2229955	NM_025112.5(ZXDC):c.170A>C (p.Glu57Ala)	LOC129937464, ZXDC (E57A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2229321	NM_025112.5(ZXDC):c.497A>C (p.Gln166Pro)	LOC129937463, ZXDC (Q166P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Links from Gene

Items: 23