Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7675161G>C | CA16603058 | TP53 | c.451C>G (p.Pro151Ala) c.55C>G (p.Pro19Ala) c.172C>G (p.Pro58Ala) c.430C>G (p.Pro144Ala) n.707C>G c.334C>G (p.Pro112Ala) c.-27C>G (n.-27C>G) c.418C>G (p.Pro140Ala) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675161G>T | CA000198 | TP53 | c.451C>A (p.Pro151Thr) c.55C>A (p.Pro19Thr) c.172C>A (p.Pro58Thr) c.430C>A (p.Pro144Thr) n.707C>A c.334C>A (p.Pro112Thr) c.-27C>A (n.-27C>A) c.418C>A (p.Pro140Thr) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675161G>A | CA000200 | TP53 | c.451C>T (p.Pro151Ser) c.55C>T (p.Pro19Ser) c.172C>T (p.Pro58Ser) c.430C>T (p.Pro144Ser) n.707C>T c.334C>T (p.Pro112Ser) c.-27C>T (n.-27C>T) c.418C>T (p.Pro140Ser) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |