Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.32807793G>ACA118461DNMT3Bc.*1403G>A (n.*1403G>A)
c.2263G>A (p.Val755Met)
c.*1006G>A (n.*1006G>A)
c.*1195G>A (n.*1195G>A)
c.2233G>A (p.Val745Met)
n.477G>A
c.2428G>A (p.Val810Met)
c.2452G>A (p.Val818Met)
c.2203G>A (p.Val735Met)
c.2392G>A (p.Val798Met)
c.2077G>A (p.Val693Met)
c.1975G>A (p.Val659Met)
c.2239G>A (p.Val747Met)
c.2113G>A (p.Val705Met)
n.2230G>A
n.2241G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
20g.32807793G>TCA9810922DNMT3Bc.*1403G>T (n.*1403G>T)
c.2263G>T (p.Val755Leu)
c.*1006G>T (n.*1006G>T)
c.*1195G>T (n.*1195G>T)
c.2233G>T (p.Val745Leu)
n.477G>T
c.2428G>T (p.Val810Leu)
c.2452G>T (p.Val818Leu)
c.2203G>T (p.Val735Leu)
c.2392G>T (p.Val798Leu)
c.2077G>T (p.Val693Leu)
c.1975G>T (p.Val659Leu)
c.2239G>T (p.Val747Leu)
c.2113G>T (p.Val705Leu)
n.2230G>T
n.2241G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched