Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.66870409A>CCA16606005PCc.796T>G (p.Ser266Ala)
n.290-20344T>G
c.676T>G (p.Ser226Ala)
ClinVar dbSNP gnomAD v4
11g.66870409A>GCA6132104PCc.796T>C (p.Ser266Pro)
n.290-20344T>C
c.676T>C (p.Ser226Pro)
dbSNP ExAC gnomAD v2
11g.66870409A>TCA341775PCc.796T>A (p.Ser266Thr)
n.290-20344T>A
c.676T>A (p.Ser226Thr)
dbSNP

Number of alleles fetched