C1866855[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 397539	NM_014946.4(SPAST):c.1111C>T (p.Leu371Phe)	SPAST (L339F +3 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia +1 more	GLikely pathogenic
Select item 226113	NM_014946.4(SPAST):c.1245+1G>A	SPAST	Single nucleotide variant (splice donor variant)	SPAST-related spastic paraplegia +4 more	GPathogenic/Likely pathogenic
Select item 2627552	NM_014946.4(SPAST):c.1441_1446del (p.Leu481_Val482del)	SPAST	Deletion (inframe_deletion)	Hereditary spastic paraplegia 4	GLikely pathogenic

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