| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7673554C>A | CA000516 | TP53 | c.974G>T (p.Gly325Val) c.578G>T (p.Gly193Val) c.695G>T (p.Gly232Val) c.953G>T (p.Gly318Val) c.782+627G>T (n.782+627G>T) c.34G>T c.857G>T (p.Gly286Val) c.497G>T (p.Gly166Val) c.941G>T (p.Gly314Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.7673554C>T | CA397835817 | TP53 | c.974G>A (p.Gly325Glu) c.578G>A (p.Gly193Glu) c.695G>A (p.Gly232Glu) c.953G>A (p.Gly318Glu) c.782+627G>A (n.782+627G>A) c.34G>A c.857G>A (p.Gly286Glu) c.497G>A (p.Gly166Glu) c.941G>A (p.Gly314Glu) | ClinVar dbSNP COSMIC |
| 17 | g.7673554C>G | CA397835813 | TP53 | c.974G>C (p.Gly325Ala) c.578G>C (p.Gly193Ala) c.695G>C (p.Gly232Ala) c.953G>C (p.Gly318Ala) c.782+627G>C (n.782+627G>C) c.34G>C c.857G>C (p.Gly286Ala) c.497G>C (p.Gly166Ala) c.941G>C (p.Gly314Ala) | dbSNP COSMIC |