Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.5002539C>TCA150725INCA1,KIF1Cc.505C>T (p.Arg169Trp)
c.-39+3543G>A (n.-39+3543G>A)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
17g.5002539C=CA2244674541INCA1,KIF1Cc.505C= (p.Arg169=)
c.-39+3543G= (n.-39+3543G=)
dbSNP

Number of alleles fetched