Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.46128885C>GCA9888651CD40c.679C>G (p.Pro227Ala)
c.*5C>G (p.=)
n.581C>G
n.652C>G
n.755C>G
c.*226C>G (p.=)
n.772C>G
c.691C>G (p.Pro231Ala)
c.535C>G (p.Pro179Ala)
n.679C>G
c.523C>G (p.Pro175Ala)
n.675C>G
c.714C>G (p.Pro238=)
c.612C>G (p.Pro204=)
n.712C>G
n.615C>G
ClinVar dbSNP ExAC gnomAD
20g.46128885C>TCA315654753CD40c.679C>T (p.Pro227Ser)
c.*5C>T (p.=)
n.581C>T
n.652C>T
n.755C>T
c.*226C>T (p.=)
n.772C>T
c.691C>T (p.Pro231Ser)
c.535C>T (p.Pro179Ser)
n.679C>T
c.523C>T (p.Pro175Ser)
n.675C>T
c.714C>T (p.Pro238=)
c.612C>T (p.Pro204=)
n.712C>T
n.615C>T
dbSNP

Number of alleles fetched