Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.189866712G>T | CA355754419 | TP63 | c.797G>T (p.Arg266Leu) c.515G>T (p.Arg172Leu) c.260G>T (p.Arg87Leu) n.621G>T c.746G>T (p.Arg249Leu) c.794G>T (p.Arg265Leu) c.791G>T (p.Arg264Leu) c.758G>T (p.Arg253Leu) | ClinVar dbSNP |
3 | g.189866712G>A | CA118348 | TP63 | c.797G>A (p.Arg266Gln) c.515G>A (p.Arg172Gln) c.260G>A (p.Arg87Gln) n.621G>A c.746G>A (p.Arg249Gln) c.794G>A (p.Arg265Gln) c.791G>A (p.Arg264Gln) c.758G>A (p.Arg253Gln) | ClinVar dbSNP COSMIC COSMIC COSMIC |
3 | g.189866712G>C | CA355754417 | TP63 | c.797G>C (p.Arg266Pro) c.515G>C (p.Arg172Pro) c.260G>C (p.Arg87Pro) n.621G>C c.746G>C (p.Arg249Pro) c.794G>C (p.Arg265Pro) c.791G>C (p.Arg264Pro) c.758G>C (p.Arg253Pro) | ClinVar dbSNP |