Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.46725727C>T | CA319966 | SLC2A10 | c.691C>T (p.Arg231Trp) c.754C>T (p.Arg252Trp) c.700C>T (p.Arg234Trp) n.890C>T n.877C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.46725727C>G | CA409267846 | SLC2A10 | c.691C>G (p.Arg231Gly) c.754C>G (p.Arg252Gly) c.700C>G (p.Arg234Gly) n.890C>G n.877C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |