Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.17024040C>T | CA015982 | SDHB | c.404G>A (p.Cys135Tyr) c.533G>A (p.Cys178Tyr) c.575G>A (p.Cys192Tyr) n.509G>A | ClinVar dbSNP |
1 | g.17024040C>G | CA015991 | SDHB | c.404G>C (p.Cys135Ser) c.533G>C (p.Cys178Ser) c.575G>C (p.Cys192Ser) n.509G>C | ClinVar dbSNP |
1 | g.17024040C= | CA1144228682 | SDHB | c.404G= (p.Cys135=) c.533G= (p.Cys178=) c.575G= (p.Cys192=) n.509G= | dbSNP |