Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.36219873delCA16041309CLTA,GNEc.1874del (p.Met625ArgfsTer?)
c.1604del (p.Met535ArgfsTer?)
c.1781del (p.Met594ArgfsTer?)
c.1559del (p.Met520ArgfsTer?)
c.485+15694del (n.485+15694del)
c.1451del (p.Met484ArgfsTer?)
c.1766del (p.Met589ArgfsTer?)
c.1721del (p.Met574ArgfsTer?)
c.1628del (p.Met543ArgfsTer?)
ClinVar dbSNP
9g.36219873A=CA1846328501CLTA,GNEc.1874T= (p.Met625=)
c.1604T= (p.Met535=)
c.1781T= (p.Met594=)
c.1559T= (p.Met520=)
c.485+15694A= (n.485+15694A=)
c.1451T= (p.Met484=)
c.1766T= (p.Met589=)
c.1721T= (p.Met574=)
c.1628T= (p.Met543=)
dbSNP dbSNP

Number of alleles fetched