Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.15601895G>TCA16040907BTDc.44+1G>T (p.=)
c.50+125G>T (p.=)
c.-139+1G>T (p.=)
c.-293+1G>T (p.=)
c.-191+1G>T (p.=)
c.-467+1G>T (p.=)
c.*295+1G>T (p.=)
c.-17+248G>T (p.=)
n.94+1G>T
n.124+1G>T
n.147+1G>T
n.401+125G>T
ClinVar dbSNP
3g.15601895G>CCA16040906BTDc.44+1G>C (p.=)
c.50+125G>C (p.=)
c.-139+1G>C (p.=)
c.-293+1G>C (p.=)
c.-191+1G>C (p.=)
c.-467+1G>C (p.=)
c.*295+1G>C (p.=)
c.-17+248G>C (p.=)
n.94+1G>C
n.124+1G>C
n.147+1G>C
n.401+125G>C
ClinVar dbSNP
3g.15601895G>ACA16040905BTDc.44+1G>A (p.=)
c.50+125G>A (p.=)
c.-139+1G>A (p.=)
c.-293+1G>A (p.=)
c.-191+1G>A (p.=)
c.-467+1G>A (p.=)
c.*295+1G>A (p.=)
c.-17+248G>A (p.=)
n.94+1G>A
n.124+1G>A
n.147+1G>A
n.401+125G>A
ClinVar dbSNP COSMIC

Number of alleles fetched