Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.25234374G>CCA16602366DNMT3Ac.893C>G
c.1790C>G (n.1790C>G)
c.1975C>G (p.Arg659Gly)
c.2644C>G (p.Arg882Gly)
c.2077C>G (p.Arg693Gly)
c.*497C>G (n.*497C>G)
c.2200C>G (p.Arg734Gly)
c.2497C>G (p.Arg833Gly)
c.2479C>G (p.Arg827Gly)
c.2188C>G (p.Arg730Gly)
c.2116C>G (p.Arg706Gly)
n.3181C>G
n.2851C>G
n.3074C>G
ClinVar dbSNP gnomAD v4 COSMIC
2g.25234374G>ACA1555491DNMT3Ac.893C>T
c.1790C>T (n.1790C>T)
c.1975C>T (p.Arg659Cys)
c.2644C>T (p.Arg882Cys)
c.2077C>T (p.Arg693Cys)
c.*497C>T (n.*497C>T)
c.2200C>T (p.Arg734Cys)
c.2497C>T (p.Arg833Cys)
c.2479C>T (p.Arg827Cys)
c.2188C>T (p.Arg730Cys)
c.2116C>T (p.Arg706Cys)
n.3181C>T
n.2851C>T
n.3074C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
2g.25234374G>TCA16602367DNMT3Ac.893C>A
c.1790C>A (n.1790C>A)
c.1975C>A (p.Arg659Ser)
c.2644C>A (p.Arg882Ser)
c.2077C>A (p.Arg693Ser)
c.*497C>A (n.*497C>A)
c.2200C>A (p.Arg734Ser)
c.2497C>A (p.Arg833Ser)
c.2479C>A (p.Arg827Ser)
c.2188C>A (p.Arg730Ser)
c.2116C>A (p.Arg706Ser)
n.3181C>A
n.2851C>A
n.3074C>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC

Number of alleles fetched