Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.44660606C>ACA344322SPG11c.268G>T (p.Glu90Ter)
n.297G>T
n.213G>T
n.299G>T
n.283G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.44660606C=CA2173717634SPG11c.268G= (p.Glu90=)
n.297G=
n.213G=
n.299G=
n.283G=
 dbSNP

Number of alleles fetched