Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674252C>GCA287488027TP53c.711G>C (p.Met237Ile)
c.315G>C (p.Met105Ile)
c.432G>C (p.Met144Ile)
c.690G>C (p.Met230Ile)
c.594G>C (p.Met198Ile)
c.234G>C (p.Met78Ile)
c.678G>C (p.Met226Ile)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7674252C>ACA287488024TP53c.711G>T (p.Met237Ile)
c.315G>T (p.Met105Ile)
c.432G>T (p.Met144Ile)
c.690G>T (p.Met230Ile)
c.594G>T (p.Met198Ile)
c.234G>T (p.Met78Ile)
c.678G>T (p.Met226Ile)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674252C>TCA000349TP53c.711G>A (p.Met237Ile)
c.315G>A (p.Met105Ile)
c.432G>A (p.Met144Ile)
c.690G>A (p.Met230Ile)
c.594G>A (p.Met198Ile)
c.234G>A (p.Met78Ile)
c.678G>A (p.Met226Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched