Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674193A>GCA397837703TP53c.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
17g.7674193A>CCA000404TP53c.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
17g.7674193A>TCA000402TP53c.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
17g.7674193A=CA2245951034TP53c.770T= (p.Leu257=)
c.374T= (p.Leu125=)
c.491T= (p.Leu164=)
c.749T= (p.Leu250=)
c.653T= (p.Leu218=)
c.293T= (p.Leu98=)
c.737T= (p.Leu246=)
dbSNP

Number of alleles fetched