"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 209166	NM_006612.6(KIF1C):c.2099C>T (p.Pro700Leu)	KIF1C (P700L)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia +2 more	GConflicting classifications of pathogenicity
Select item 390925	NM_006612.6(KIF1C):c.3071G>A (p.Arg1024Gln)	KIF1C (R1024Q)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia +2 more	GLikely benign