Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.48368549C>T | CA026363 | RB1 | c.1072C>T (p.Arg358Ter) c.811C>T (p.Arg271Ter) n.122-3573G>A | ClinVar dbSNP COSMIC COSMIC |
13 | g.48368549C>G | CA388161148 | RB1 | c.1072C>G (p.Arg358Gly) c.811C>G (p.Arg271Gly) n.122-3573G>C | ClinVar dbSNP |
13 | g.48368549C= | CA2089983824 | RB1 | c.1072C= (p.Arg358=) c.811C= (p.Arg271=) n.122-3573G= | dbSNP |