Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.113049143G>ACA214111593TCF7L2c.552+9017G>A (p.=)
c.483+9017G>A (p.=)
c.382-92041G>A (p.=)
c.93+9017G>A (p.=)
n.393+9017G>A (p.=)
c.165+9017G>A (p.=)
n.483+9017G>A (p.=)
dbSNP
10g.113049143G>TCA118787TCF7L2c.552+9017G>T (p.=)
c.483+9017G>T (p.=)
c.382-92041G>T (p.=)
c.93+9017G>T (p.=)
n.393+9017G>T (p.=)
c.165+9017G>T (p.=)
n.483+9017G>T (p.=)
ClinVar dbSNP gnomAD

Number of alleles fetched