| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.63665930G>A | CA358247 | ARHGEF9 | c.949C>T (p.Arg317Trp) c.1051C>T (p.Arg351Trp) c.*890C>T (n.*890C>T) c.1012C>T (p.Arg338Trp) c.826C>T (p.Arg276Trp) c.734C>T c.*910C>T (n.*910C>T) c.1033C>T (p.Arg345Trp) c.931C>T (p.Arg311Trp) n.1102C>T c.861+8108C>T (n.861+8108C>T) c.189C>T c.*781+8108C>T (n.*781+8108C>T) c.853C>T (p.Arg285Trp) c.706C>T (p.Arg236Trp) c.832C>T (p.Arg278Trp) c.945+8108C>T (n.945+8108C>T) c.924+8108C>T (n.924+8108C>T) c.1027C>T (p.Arg343Trp) c.744+8108C>T (n.744+8108C>T) c.1006C>T (p.Arg336Trp) c.510+8108C>T (n.510+8108C>T) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| X | g.63665930G= | CA2433124421 | ARHGEF9 | c.949C= (p.Arg317=) c.1051C= (p.Arg351=) c.*890C= (n.*890C=) c.1012C= (p.Arg338=) c.826C= (p.Arg276=) c.734C= c.*910C= (n.*910C=) c.1033C= (p.Arg345=) c.931C= (p.Arg311=) n.1102C= c.861+8108C= (n.861+8108C=) c.189C= c.*781+8108C= (n.*781+8108C=) c.853C= (p.Arg285=) c.706C= (p.Arg236=) c.832C= (p.Arg278=) c.945+8108C= (n.945+8108C=) c.924+8108C= (n.924+8108C=) c.1027C= (p.Arg343=) c.744+8108C= (n.744+8108C=) c.1006C= (p.Arg336=) c.510+8108C= (n.510+8108C=) | dbSNP |