Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.99818820C>ACA212848412ABCC2c.2302C>A (p.Arg768=)
c.1606C>A (p.Arg536=)
n.2491C>A
n.2493C>A
n.2545C>A
dbSNP gnomAD
10g.99818820C>TCA119596ABCC2c.2302C>T (p.Arg768Trp)
c.1606C>T (p.Arg536Trp)
n.2491C>T
n.2493C>T
n.2545C>T
ClinVar dbSNP ExAC gnomAD COSMIC
10g.99818820C>GCA212848411ABCC2c.2302C>G (p.Arg768Gly)
c.1606C>G (p.Arg536Gly)
n.2491C>G
n.2493C>G
n.2545C>G
dbSNP

Number of alleles fetched