Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.25209843A>G | CA135582 | KRAS | c.180T>C (p.Asp60=) c.519T>C (p.Asp173=) c.*490T>C (n.*490T>C) c.*217T>C (n.*217T>C) n.993T>C c.322T>C c.*480T>C (n.*480T>C) c.321T>C (p.Asp107=) c.444T>C (p.Asp148=) c.*73T>C (n.*73T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.25209843A>T | CA234206915 | KRAS | c.180T>A (p.Asp60Glu) c.519T>A (p.Asp173Glu) c.*490T>A (n.*490T>A) c.*217T>A (n.*217T>A) n.993T>A c.322T>A c.*480T>A (n.*480T>A) c.321T>A (p.Asp107Glu) c.444T>A (p.Asp148Glu) c.*73T>A (n.*73T>A) | dbSNP |