Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.25209843A>GCA135582KRASc.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
12g.25209843A>TCA234206915KRASc.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
12g.25209843A=CA2022884601KRASc.180T= (p.Asp60=)
c.519T= (p.Asp173=)
c.*490T= (n.*490T=)
c.*217T= (n.*217T=)
n.993T=
c.322T=
c.*480T= (n.*480T=)
c.321T= (p.Asp107=)
c.444T= (p.Asp148=)
c.*73T= (n.*73T=)
dbSNP

Number of alleles fetched