"ZFP36L2-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3044335	NM_006887.5(ZFP36L2):c.1227G>A (p.Pro409=)	ZFP36L2	Single nucleotide variant (synonymous variant)	ZFP36L2-related disorder	GLikely benign
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 3048852	NM_006887.5(ZFP36L2):c.835C>T (p.Leu279=)	ZFP36L2	Single nucleotide variant (synonymous variant)	ZFP36L2-related disorder	GLikely benign
Select item 3056889	NM_006887.5(ZFP36L2):c.760T>C (p.Leu254=)	ZFP36L2	Single nucleotide variant (synonymous variant)	ZFP36L2-related disorder	GBenign
Select item 3049253	NM_006887.5(ZFP36L2):c.657C>G (p.Asp219Glu)	ZFP36L2 (D219E)	Single nucleotide variant (missense variant)	ZFP36L2-related disorder	GLikely benign
Select item 3055927	NM_006887.5(ZFP36L2):c.609C>T (p.Ile203=)	ZFP36L2	Single nucleotide variant (synonymous variant)	ZFP36L2-related disorder	GBenign
Select item 3057271	NM_006887.5(ZFP36L2):c.531G>T (p.Ala177=)	ZFP36L2	Single nucleotide variant (synonymous variant)	ZFP36L2-related disorder	GLikely benign
Select item 3036014	NM_006887.5(ZFP36L2):c.489G>A (p.Glu163=)	ZFP36L2	Single nucleotide variant (synonymous variant)	ZFP36L2-related disorder	GLikely benign
Select item 3039683	NM_006887.5(ZFP36L2):c.335T>A (p.Leu112Gln)	ZFP36L2 (L112Q)	Single nucleotide variant (missense variant)	ZFP36L2-related disorder	GBenign
Select item 3050189	NM_006887.5(ZFP36L2):c.279C>T (p.Gly93=)	ZFP36L2	Single nucleotide variant (synonymous variant)	ZFP36L2-related disorder	GLikely benign
Select item 3045315	NM_006887.5(ZFP36L2):c.186T>G (p.His62Gln)	ZFP36L2 (H62Q)	Single nucleotide variant (missense variant)	ZFP36L2-related disorder	GBenign