Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7675125A>CCA000239TP53c.487T>G (p.Tyr163Asp)
c.91T>G (p.Tyr31Asp)
c.208T>G (p.Tyr70Asp)
c.466T>G (p.Tyr156Asp)
n.743T>G
c.370T>G (p.Tyr124Asp)
c.10T>G (p.Tyr4Asp)
c.454T>G (p.Tyr152Asp)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7675125A>GCA16603094TP53c.487T>C (p.Tyr163His)
c.91T>C (p.Tyr31His)
c.208T>C (p.Tyr70His)
c.466T>C (p.Tyr156His)
n.743T>C
c.370T>C (p.Tyr124His)
c.10T>C (p.Tyr4His)
c.454T>C (p.Tyr152His)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7675125A>TCA16603093TP53c.487T>A (p.Tyr163Asn)
c.91T>A (p.Tyr31Asn)
c.208T>A (p.Tyr70Asn)
c.466T>A (p.Tyr156Asn)
n.743T>A
c.370T>A (p.Tyr124Asn)
c.10T>A (p.Tyr4Asn)
c.454T>A (p.Tyr152Asn)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched