| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7676040C>A | CA002845 | TP53 | c.329G>T (p.Arg110Leu) c.-21-804G>T (n.-21-804G>T) c.96+342G>T (n.96+342G>T) n.585G>T c.212G>T (p.Arg71Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7676040C>G | CA10580948 | TP53 | c.329G>C (p.Arg110Pro) c.-21-804G>C (n.-21-804G>C) c.96+342G>C (n.96+342G>C) n.585G>C c.212G>C (p.Arg71Pro) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7676040C>T | CA000123 | TP53 | c.329G>A (p.Arg110His) c.-21-804G>A (n.-21-804G>A) c.96+342G>A (n.96+342G>A) n.585G>A c.212G>A (p.Arg71His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |