ClinVar (all) for Orgtrack (Select 505235) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 39126	NM_198253.3(TERT):c.915G>A (p.Ala305=)	TERT	Single nucleotide variant (synonymous variant +1 more)	Dyskeratosis congenita, autosomal dominant 2 +11 more	GBenign
Select item 39118	NM_198253.3(TERT):c.2935C>T (p.Arg979Trp)	TERT (R979W +1 more)	Single nucleotide variant (missense variant +1 more)	Idiopathic Pulmonary Fibrosis +1 more	GUncertain significance