| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7673803G>A | CA000432 | TP53 | c.817C>T (p.Arg273Cys) c.421C>T (p.Arg141Cys) c.538C>T (p.Arg180Cys) c.796C>T (p.Arg266Cys) c.782+378C>T (n.782+378C>T) c.700C>T (p.Arg234Cys) c.340C>T (p.Arg114Cys) c.784C>T (p.Arg262Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673803G>T | CA001542 | TP53 | c.817C>A (p.Arg273Ser) c.421C>A (p.Arg141Ser) c.538C>A (p.Arg180Ser) c.796C>A (p.Arg266Ser) c.782+378C>A (n.782+378C>A) c.700C>A (p.Arg234Ser) c.340C>A (p.Arg114Ser) c.784C>A (p.Arg262Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673803G>C | CA397836977 | TP53 | c.817C>G (p.Arg273Gly) c.421C>G (p.Arg141Gly) c.538C>G (p.Arg180Gly) c.796C>G (p.Arg266Gly) c.782+378C>G (n.782+378C>G) c.700C>G (p.Arg234Gly) c.340C>G (p.Arg114Gly) c.784C>G (p.Arg262Gly) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |