"Institute of Human Genetics, University of Leipzig Medical Center"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1804141	NM_080632.3(UPF3B):c.1147G>T (p.Glu383Ter)	UPF3B (E370* +1 more)	Single nucleotide variant (nonsense)	Syndromic X-linked intellectual disability 14	GLikely pathogenic
Select item 1712323	NM_080632.3(UPF3B):c.270T>G (p.Tyr90Ter)	UPF3B (Y90*)	Single nucleotide variant (nonsense)	Syndromic X-linked intellectual disability 14	GLikely pathogenic