Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.95111502G>ACA350781C9orf3,FANCCc.1290C>T (p.Tyr430=)
c.609C>T (p.Tyr203=)
c.1125C>T (p.Tyr375=)
c.834C>T (p.Tyr278=)
c.2319+30722G>A (p.=)
c.669C>T (p.Tyr223=)
n.617C>T
n.645C>T
n.475C>T
ClinVar dbSNP ExAC gnomAD COSMIC
9g.95111502G>TCA349399C9orf3,FANCCc.1290C>A (p.Tyr430Ter)
c.609C>A (p.Tyr203Ter)
c.1125C>A (p.Tyr375Ter)
c.834C>A (p.Tyr278Ter)
c.2319+30722G>T (p.=)
c.669C>A (p.Tyr223Ter)
n.617C>A
n.645C>A
n.475C>A
ClinVar dbSNP

Number of alleles fetched