Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.17054012G>A | CA338230874 | SDHB | c.8C>T (p.Ala3Val) n.20C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.17054012G>C | CA016202 | SDHB | c.8C>G (p.Ala3Gly) n.20C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.17054012G>T | CA338230876 | SDHB | c.8C>A (p.Ala3Glu) n.20C>A | ClinVar dbSNP gnomAD v4 |