Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.5960405T>GCA5397051IL15RAc.545A>C (p.Asn182Thr)
c.251A>C (p.Asn84Thr)
n.670A>C
n.566A>C
c.338A>C (p.Asn113Thr)
c.803A>C (p.Asn268Thr)
c.698A>C (p.Asn233Thr)
c.446A>C (p.Asn149Thr)
c.163A>C
c.253A>C
c.434A>C (p.Asn145Thr)
c.437A>C (p.Asn146Thr)
c.259A>C
n.620A>C
n.726A>C
n.574A>C
c.872A>C (p.Asn291Thr)
c.773A>C (p.Asn258Thr)
c.719A>C (p.Asn240Thr)
c.650A>C (p.Asn217Thr)
c.551A>C (p.Asn184Thr)
c.524A>C (p.Asn175Thr)
c.455A>C (p.Asn152Thr)
c.425A>C (p.Asn142Thr)
c.356A>C (p.Asn119Thr)
c.620A>C (p.Asn207Thr)
n.613T>G
n.433A>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.5960405T>CCA375927995IL15RAc.545A>G (p.Asn182Ser)
c.251A>G (p.Asn84Ser)
n.670A>G
n.566A>G
c.338A>G (p.Asn113Ser)
c.803A>G (p.Asn268Ser)
c.698A>G (p.Asn233Ser)
c.446A>G (p.Asn149Ser)
c.163A>G
c.253A>G
c.434A>G (p.Asn145Ser)
c.437A>G (p.Asn146Ser)
c.259A>G
n.620A>G
n.726A>G
n.574A>G
c.872A>G (p.Asn291Ser)
c.773A>G (p.Asn258Ser)
c.719A>G (p.Asn240Ser)
c.650A>G (p.Asn217Ser)
c.551A>G (p.Asn184Ser)
c.524A>G (p.Asn175Ser)
c.455A>G (p.Asn152Ser)
c.425A>G (p.Asn142Ser)
c.356A>G (p.Asn119Ser)
c.620A>G (p.Asn207Ser)
n.613T>C
n.433A>G
dbSNP

Number of alleles fetched