Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.6690936G>ACA210672ALOX15P1,C17orf100,SLC13A5c.1280C>T (p.Ser427Leu)
n.725-1929G>A
c.1229C>T (p.Ser410Leu)
c.1151C>T (p.Ser384Leu)
n.389C>T
n.662+909G>A
n.265-1929G>A
c.1169C>T (p.Ser390Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.6690936G=CA2245485286ALOX15P1,C17orf100,SLC13A5c.1280C= (p.Ser427=)
n.725-1929G=
c.1229C= (p.Ser410=)
c.1151C= (p.Ser384=)
n.389C=
n.662+909G=
n.265-1929G=
c.1169C= (p.Ser390=)
dbSNP

Number of alleles fetched