"TNFRSF25-related disorder"[Disease/phenotype] AND "PreventionGenetics - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3050556	NM_003790.3(TNFRSF25):c.1047G>A (p.Glu349=)	TNFRSF25	Single nucleotide variant (synonymous variant)	TNFRSF25-related disorder	GLikely benign
Select item 3051801	NM_003790.3(TNFRSF25):c.816C>T (p.Cys272=)	TNFRSF25	Single nucleotide variant (synonymous variant)	TNFRSF25-related disorder	GLikely benign
Select item 789686	NM_003790.3(TNFRSF25):c.745-10T>C	TNFRSF25	Single nucleotide variant (intron variant)	TNFRSF25-related disorder +1 more	GLikely benign
Select item 3034589	NM_003790.3(TNFRSF25):c.696C>T (p.Pro232=)	TNFRSF25	Single nucleotide variant (synonymous variant +1 more)	TNFRSF25-related disorder	GLikely benign
Select item 3056652	NM_003790.3(TNFRSF25):c.476A>G (p.Asp159Gly)	TNFRSF25 (D114G +1 more)	Single nucleotide variant (missense variant +1 more)	TNFRSF25-related disorder	GBenign
Select item 3056091	NM_003790.3(TNFRSF25):c.387A>G (p.Gln129=)	TNFRSF25	Single nucleotide variant (synonymous variant +1 more)	TNFRSF25-related disorder	GBenign
Select item 3044857	NM_003790.3(TNFRSF25):c.372G>A (p.Glu124=)	TNFRSF25	Single nucleotide variant (synonymous variant +1 more)	TNFRSF25-related disorder	GBenign
Select item 3049400	NM_003790.3(TNFRSF25):c.108C>T (p.Ala36=)	TNFRSF25	Single nucleotide variant (synonymous variant)	TNFRSF25-related disorder	GLikely benign
Select item 3058208	NM_003790.3(TNFRSF25):c.72C>T (p.Ala24=)	TNFRSF25	Single nucleotide variant (synonymous variant)	TNFRSF25-related disorder	GLikely benign