Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7674193A>G | CA397837703 | TP53 | c.770T>C (p.Leu257Pro) c.374T>C (p.Leu125Pro) c.491T>C (p.Leu164Pro) c.749T>C (p.Leu250Pro) c.653T>C (p.Leu218Pro) c.293T>C (p.Leu98Pro) c.737T>C (p.Leu246Pro) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674193A>C | CA000404 | TP53 | c.770T>G (p.Leu257Arg) c.374T>G (p.Leu125Arg) c.491T>G (p.Leu164Arg) c.749T>G (p.Leu250Arg) c.653T>G (p.Leu218Arg) c.293T>G (p.Leu98Arg) c.737T>G (p.Leu246Arg) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674193A>T | CA000402 | TP53 | c.770T>A (p.Leu257Gln) c.374T>A (p.Leu125Gln) c.491T>A (p.Leu164Gln) c.749T>A (p.Leu250Gln) c.653T>A (p.Leu218Gln) c.293T>A (p.Leu98Gln) c.737T>A (p.Leu246Gln) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |