Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7673824C>TCA397837142TP53c.796G>A (p.Gly266Arg)
c.400G>A (p.Gly134Arg)
c.517G>A (p.Gly173Arg)
c.775G>A (p.Gly259Arg)
c.782+357G>A (n.782+357G>A)
c.679G>A (p.Gly227Arg)
c.319G>A (p.Gly107Arg)
c.763G>A (p.Gly255Arg)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673824C>GCA16603026TP53c.796G>C (p.Gly266Arg)
c.400G>C (p.Gly134Arg)
c.517G>C (p.Gly173Arg)
c.775G>C (p.Gly259Arg)
c.782+357G>C (n.782+357G>C)
c.679G>C (p.Gly227Arg)
c.319G>C (p.Gly107Arg)
c.763G>C (p.Gly255Arg)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673824C>ACA397837139TP53c.796G>T (p.Gly266Ter)
c.400G>T (p.Gly134Ter)
c.517G>T (p.Gly173Ter)
c.775G>T (p.Gly259Ter)
c.782+357G>T (n.782+357G>T)
c.679G>T (p.Gly227Ter)
c.319G>T (p.Gly107Ter)
c.763G>T (p.Gly255Ter)
ClinVar dbSNP gnomAD v2 COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched