Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.101786009T>CCA6746856GNPTABc.571+3A>G (p.=)
c.490+3A>G (p.=)
c.355+3A>G (p.=)
c.-780+3A>G (p.=)
n.368A>G
n.205+3A>G (p.=)
dbSNP ExAC
12g.101786009T>GCA343410GNPTABc.571+3A>C (p.=)
c.490+3A>C (p.=)
c.355+3A>C (p.=)
c.-780+3A>C (p.=)
n.368A>C
n.205+3A>C (p.=)
ClinVar dbSNP

Number of alleles fetched