Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674217C>TCA000391TP53c.746G>A (p.Arg249Lys)
c.350G>A (p.Arg117Lys)
c.467G>A (p.Arg156Lys)
c.725G>A (p.Arg242Lys)
c.467G>A
c.629G>A (p.Arg210Lys)
c.269G>A (p.Arg90Lys)
c.713G>A (p.Arg238Lys)
ClinVar dbSNP COSMIC COSMIC COSMIC
17g.7674217C>ACA16603070TP53c.746G>T (p.Arg249Met)
c.350G>T (p.Arg117Met)
c.467G>T (p.Arg156Met)
c.725G>T (p.Arg242Met)
c.467G>T
c.629G>T (p.Arg210Met)
c.269G>T (p.Arg90Met)
c.713G>T (p.Arg238Met)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674217C>GCA16602484TP53c.746G>C (p.Arg249Thr)
c.350G>C (p.Arg117Thr)
c.467G>C (p.Arg156Thr)
c.725G>C (p.Arg242Thr)
c.467G>C
c.629G>C (p.Arg210Thr)
c.269G>C (p.Arg90Thr)
c.713G>C (p.Arg238Thr)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674217C=CA2245951325TP53c.746G= (p.Arg249=)
c.350G= (p.Arg117=)
c.467G= (p.Arg156=)
c.725G= (p.Arg242=)
c.467G=
c.629G= (p.Arg210=)
c.269G= (p.Arg90=)
c.713G= (p.Arg238=)
dbSNP

Number of alleles fetched