Related gene-specific medical variations for Gene (Select 678) - ClinVar - NCBI

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Links from Gene

Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3350739	NM_006887.5(ZFP36L2):c.1170C>T (p.Ala390=)	LOC129933607, ZFP36L2	Single nucleotide variant (synonymous variant)	ZFP36L2-related disorder	GLikely benign
Select item 3334480	NM_006887.5(ZFP36L2):c.897C>G (p.Cys299Trp)	LOC129933608, ZFP36L2 (C299W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334479	NM_006887.5(ZFP36L2):c.1123C>T (p.Pro375Ser)	LOC129933607, ZFP36L2 (P375S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334478	NM_006887.5(ZFP36L2):c.1010C>A (p.Thr337Asn)	LOC129933607, ZFP36L2 (T337N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3056057	NM_006887.5(ZFP36L2):c.986C>T (p.Ala329Val)	LOC129933607, ZFP36L2 (A329V)	Single nucleotide variant (missense variant)	ZFP36L2-related disorder	GBenign
Select item 2650851	NM_006887.5(ZFP36L2):c.1041G>A (p.Gly347=)	LOC129933607, ZFP36L2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2554559	NM_006887.5(ZFP36L2):c.1205G>T (p.Gly402Val)	LOC129933607, ZFP36L2 (G402V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552328	NM_006887.5(ZFP36L2):c.989C>T (p.Ala330Val)	LOC129933607, ZFP36L2 (A330V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486018	NM_006887.5(ZFP36L2):c.1177C>T (p.Arg393Cys)	LOC129933607, ZFP36L2 (R393C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483360	NM_006887.5(ZFP36L2):c.1160C>T (p.Ala387Val)	LOC129933607, ZFP36L2 (A387V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477618	NM_006887.5(ZFP36L2):c.1067C>T (p.Ala356Val)	LOC129933607, ZFP36L2 (A356V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465996	NM_006887.5(ZFP36L2):c.985G>A (p.Ala329Thr)	LOC129933607, ZFP36L2 (A329T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456877	NM_006887.5(ZFP36L2):c.1043C>A (p.Ala348Asp)	LOC129933607, ZFP36L2 (A348D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403750	NM_006887.5(ZFP36L2):c.1188G>C (p.Gln396His)	LOC129933607, ZFP36L2 (Q396H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365974	NM_006887.5(ZFP36L2):c.1051G>T (p.Ala351Ser)	LOC129933607, ZFP36L2 (A351S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331637	NM_006887.5(ZFP36L2):c.1091C>T (p.Ala364Val)	LOC129933607, ZFP36L2 (A364V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329758	NM_006887.5(ZFP36L2):c.1129G>C (p.Ala377Pro)	LOC129933607, ZFP36L2 (A377P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215384	NM_006887.5(ZFP36L2):c.1090G>A (p.Ala364Thr)	LOC129933607, ZFP36L2 (A364T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 585082	NM_006887.5(ZFP36L2):c.1426dup (p.Ser476fs)	ZFP36L2, LOC129933606 (S476fs)	Duplication (frameshift variant)	not provided	Gnot provided