Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.105601349G>CCA5170377FKTNc.369+1G>C (p.=)
c.300+1G>C (p.=)
c.183+1G>C (p.=)
c.-125+1G>C (p.=)
c.-146+1G>C (p.=)
n.585+1G>C
n.493+1G>C
c.369+1G>C
c.300+1G>C
c.183+1G>C
c.-125+1G>C
n.733+1G>C
n.583+1G>C
n.1558+1G>C
c.*289+1G>C (p.=)
dbSNP ExAC gnomAD
9g.105601349G>TCA10581277FKTNc.369+1G>T (p.=)
c.300+1G>T (p.=)
c.183+1G>T (p.=)
c.-125+1G>T (p.=)
c.-146+1G>T (p.=)
n.585+1G>T
n.493+1G>T
c.369+1G>T
c.300+1G>T
c.183+1G>T
c.-125+1G>T
n.733+1G>T
n.583+1G>T
n.1558+1G>T
c.*289+1G>T (p.=)
ClinVar dbSNP COSMIC

Number of alleles fetched