C1863704[trait identifier] AND "Center of Genomic medicine, Geneva, Un - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1162	NM_014846.4(WASHC5):c.1857G>C (p.Leu619Phe)	WASHC5 (L619F +1 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 8 +1 more	GPathogenic
Select item 495056	NM_014846.4(WASHC5):c.1772C>T (p.Ser591Phe)	WASHC5 (S591F +1 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 8 +2 more	GPathogenic/Likely pathogenic