Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.17023975G>C | CA338270926 | SDHB | c.469C>G (p.Gln157Glu) c.598C>G (p.Gln200Glu) c.640C>G (p.Gln214Glu) n.574C>G | dbSNP |
1 | g.17023975G>A | CA10577671 | SDHB | c.469C>T (p.Gln157Ter) c.598C>T (p.Gln200Ter) c.640C>T (p.Gln214Ter) n.574C>T | ClinVar dbSNP |
1 | g.17023975G= | CA1156078612 | SDHB | c.469C= (p.Gln157=) c.598C= (p.Gln200=) c.640C= (p.Gln214=) n.574C= | dbSNP |