rs587777198

This is a variant in the KIF1C gene that changes a arginine to an tryptophan.

ClinVar annotation

Pathogenic☆☆☆
2 submitters1 publication

Spastic ataxia 2

View on ClinVar →

About KIF1C

The protein encoded by this gene is a member of the kinesin-like protein family. The family members are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. Mutations in this gene are a cause of spastic ataxia 2, autosomal recessive. [provided by RefSeq, May 2014]

View all KIF1C variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Sign in to join the discussion.

Loading comments…