Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674211A>CCA000396TP53c.752T>G (p.Ile251Ser)
c.356T>G (p.Ile119Ser)
c.473T>G (p.Ile158Ser)
c.731T>G (p.Ile244Ser)
c.635T>G (p.Ile212Ser)
c.275T>G (p.Ile92Ser)
c.719T>G (p.Ile240Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 COSMIC
17g.7674211A>GCA397838899TP53c.752T>C (p.Ile251Thr)
c.356T>C (p.Ile119Thr)
c.473T>C (p.Ile158Thr)
c.731T>C (p.Ile244Thr)
c.635T>C (p.Ile212Thr)
c.275T>C (p.Ile92Thr)
c.719T>C (p.Ile240Thr)
ClinVar dbSNP
17g.7674211A>TCA397838901TP53c.752T>A (p.Ile251Asn)
c.356T>A (p.Ile119Asn)
c.473T>A (p.Ile158Asn)
c.731T>A (p.Ile244Asn)
c.635T>A (p.Ile212Asn)
c.275T>A (p.Ile92Asn)
c.719T>A (p.Ile240Asn)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched