Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.136506852G>CCA375549387NOTCH1n.1572C>G
c.3765C>G (p.Cys1255Trp)
c.3651C>G (p.Cys1217Trp)
c.1362C>G (p.Cys454Trp)
c.*1165C>G (n.*1165C>G)
c.*1374C>G (n.*1374C>G)
n.578C>G
c.*3001C>G (n.*3001C>G)
c.3066C>G (p.Cys1022Trp)
c.3042C>G (p.Cys1014Trp)
dbSNP
9g.136506852G>ACA467833453NOTCH1n.1572C>T
c.3765C>T (p.Cys1255=)
c.3651C>T (p.Cys1217=)
c.1362C>T (p.Cys454=)
c.*1165C>T (n.*1165C>T)
c.*1374C>T (n.*1374C>T)
n.578C>T
c.*3001C>T (n.*3001C>T)
c.3066C>T (p.Cys1022=)
c.3042C>T (p.Cys1014=)
dbSNP
9g.136506852G>TCA10602396NOTCH1n.1572C>A
c.3765C>A (p.Cys1255Ter)
c.3651C>A (p.Cys1217Ter)
c.1362C>A (p.Cys454Ter)
c.*1165C>A (n.*1165C>A)
c.*1374C>A (n.*1374C>A)
n.578C>A
c.*3001C>A (n.*3001C>A)
c.3066C>A (p.Cys1022Ter)
c.3042C>A (p.Cys1014Ter)
ClinVar dbSNP

Number of alleles fetched