Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.72233098C>T | CA130326 | INPPL1 | c.1975C>T (p.Pro659Ser) c.1249C>T (p.Pro417Ser) n.581C>T c.1777C>T (p.Pro593Ser) n.128C>T c.2041C>T (p.Pro681Ser) c.2011C>T (p.Pro671Ser) | ClinVar dbSNP |
11 | g.72233098C= | CA1981899363 | INPPL1 | c.1975C= (p.Pro659=) c.1249C= (p.Pro417=) n.581C= c.1777C= (p.Pro593=) n.128C= c.2041C= (p.Pro681=) c.2011C= (p.Pro671=) | dbSNP |