Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.127738435C>T | CA16602746 | MYC | c.173C>T (p.Thr58Ile) c.215C>T (p.Thr72Ile) c.218C>T (p.Thr73Ile) c.-128C>T (n.-128C>T) c.139C>T (p.Pro47Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
8 | g.127738435C>G | CA4875251 | MYC | c.173C>G (p.Thr58Ser) c.215C>G (p.Thr72Ser) c.218C>G (p.Thr73Ser) c.-128C>G (n.-128C>G) c.139C>G (p.Pro47Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.127738435C= | CA1818466441 | MYC | c.173C= (p.Thr58=) c.215C= (p.Thr72=) c.218C= (p.Thr73=) c.-128C= (n.-128C=) c.139C= (p.Pro47=) | dbSNP |