Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.17027848A>C | CA16609941 | SDHB | c.270T>G (p.Tyr90Ter) c.399T>G (p.Tyr133Ter) c.441T>G (p.Tyr147Ter) n.358T>G n.375T>G | ClinVar dbSNP |
1 | g.17027848A>G | CA416086308 | SDHB | c.270T>C (p.Tyr90=) c.399T>C (p.Tyr133=) c.441T>C (p.Tyr147=) n.358T>C n.375T>C | ClinVar dbSNP |