Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.34859485C>T | CA248610 | RUNX1 | c.602G>A (p.Arg201Gln) c.521G>A (p.Arg174Gln) c.566G>A (p.Arg189Gln) n.94G>A c.*192G>A (n.*192G>A) c.563G>A (p.Arg188Gln) n.781G>A c.449G>A (p.Arg150Gln) n.828G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
21 | g.34859485C= | CA2387284472 | RUNX1 | c.602G= (p.Arg201=) c.521G= (p.Arg174=) c.566G= (p.Arg189=) n.94G= c.*192G= (n.*192G=) c.563G= (p.Arg188=) n.781G= c.449G= (p.Arg150=) n.828G= | dbSNP |
21 | g.34859485C>G | CA410207956 | RUNX1 | c.602G>C (p.Arg201Pro) c.521G>C (p.Arg174Pro) c.566G>C (p.Arg189Pro) n.94G>C c.*192G>C (n.*192G>C) c.563G>C (p.Arg188Pro) n.781G>C c.449G>C (p.Arg150Pro) n.828G>C | dbSNP |