Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674230C>GCA16603025TP53c.733G>C (p.Gly245Arg)
c.337G>C (p.Gly113Arg)
c.454G>C (p.Gly152Arg)
c.712G>C (p.Gly238Arg)
c.616G>C (p.Gly206Arg)
c.256G>C (p.Gly86Arg)
c.700G>C (p.Gly234Arg)
ClinVar dbSNP gnomAD v2 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674230C>ACA000369TP53c.733G>T (p.Gly245Cys)
c.337G>T (p.Gly113Cys)
c.454G>T (p.Gly152Cys)
c.712G>T (p.Gly238Cys)
c.616G>T (p.Gly206Cys)
c.256G>T (p.Gly86Cys)
c.700G>T (p.Gly234Cys)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674230C>TCA000367TP53c.733G>A (p.Gly245Ser)
c.337G>A (p.Gly113Ser)
c.454G>A (p.Gly152Ser)
c.712G>A (p.Gly238Ser)
c.616G>A (p.Gly206Ser)
c.256G>A (p.Gly86Ser)
c.700G>A (p.Gly234Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched