Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.6690936G>A | CA210672 | ALOX15P1,C17orf100,SLC13A5 | c.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 |
17 | g.6690936G= | CA2245485286 | ALOX15P1,C17orf100,SLC13A5 | c.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 |