Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.197429555G>ACA279259CRB1c.2783G>A (p.Cys928Tyr)
c.1664G>A (p.Cys555Tyr)
c.926G>A (p.Cys309Tyr)
c.2447G>A (p.Cys816Tyr)
c.2711G>A (p.Cys904Tyr)
c.2129-6045G>A (n.2129-6045G>A)
n.2784G>A
n.2992G>A
c.2201G>A (p.Cys734Tyr)
c.1226G>A (p.Cys409Tyr)
c.1940G>A (p.Cys647Tyr)
c.2918G>A (p.Cys973Tyr)
n.2736G>A
n.2944G>A
ClinVar dbSNP gnomAD v4
1g.197429555G=CA1218065689CRB1c.2783G= (p.Cys928=)
c.1664G= (p.Cys555=)
c.926G= (p.Cys309=)
c.2447G= (p.Cys816=)
c.2711G= (p.Cys904=)
c.2129-6045G= (n.2129-6045G=)
n.2784G=
n.2992G=
c.2201G= (p.Cys734=)
c.1226G= (p.Cys409=)
c.1940G= (p.Cys647=)
c.2918G= (p.Cys973=)
n.2736G=
n.2944G=
dbSNP

Number of alleles fetched