Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.71755957T>GCA99065302GCc.1034+755A>C (p.=)
n.918+755A>C
c.1091+755A>C (p.=)
dbSNP gnomAD
4g.71755957T=CA1467372841GCc.1034+755A= (p.=)
n.918+755A=
c.1091+755A= (p.=)
4g.71755962C=CA1467372842GCc.1034+750G= (p.=)
n.918+750G=
c.1091+750G= (p.=)
4g.71755962C>TCA99065315GCc.1034+750G>A (p.=)
n.918+750G>A
c.1091+750G>A (p.=)
dbSNP gnomAD
4g.71755964A=CA1467372843GCc.1034+748T= (p.=)
n.918+748T=
c.1091+748T= (p.=)
4g.71755964A>GCA99065318GCc.1034+748T>C (p.=)
n.918+748T>C
c.1091+748T>C (p.=)
dbSNP
4g.71755967A=CA1467372844GCc.1034+745T= (p.=)
n.918+745T=
c.1091+745T= (p.=)
4g.71755967A>TCA1467372845GCc.1034+745T>A (p.=)
n.918+745T>A
c.1091+745T>A (p.=)
4g.71755970A=CA1467372846GCc.1034+742T= (p.=)
n.918+742T=
c.1091+742T= (p.=)
4g.71755970A>TCA99065322GCc.1034+742T>A (p.=)
n.918+742T>A
c.1091+742T>A (p.=)
dbSNP
4g.71755974A=CA1467372847GCc.1034+738T= (p.=)
n.918+738T=
c.1091+738T= (p.=)
4g.71755974A>GCA1063992463GCc.1034+738T>C (p.=)
n.918+738T>C
c.1091+738T>C (p.=)
4g.71755980A=CA1467372848GCc.1034+732T= (p.=)
n.918+732T=
c.1091+732T= (p.=)
4g.71755980A>GCA99065326GCc.1034+732T>C (p.=)
n.918+732T>C
c.1091+732T>C (p.=)
dbSNP
4g.71755984A=CA1467372849GCc.1034+728T= (p.=)
n.918+728T=
c.1091+728T= (p.=)
4g.71755984A>GCA1467372850GCc.1034+728T>C (p.=)
n.918+728T>C
c.1091+728T>C (p.=)
4g.71755988A=CA1467372851GCc.1034+724T= (p.=)
n.918+724T=
c.1091+724T= (p.=)
4g.71755988A>TCA1467372852GCc.1034+724T>A (p.=)
n.918+724T>A
c.1091+724T>A (p.=)
4g.71755996G>ACA1467372854GCc.1034+716C>T (p.=)
n.918+716C>T
c.1091+716C>T (p.=)
4g.71755996G=CA1467372853GCc.1034+716C= (p.=)
n.918+716C=
c.1091+716C= (p.=)
4g.71755996G>TCA1063992465GCc.1034+716C>A (p.=)
n.918+716C>A
c.1091+716C>A (p.=)
4g.71755997T>CCA1467372856GCc.1034+715A>G (p.=)
n.918+715A>G
c.1091+715A>G (p.=)
4g.71755997T=CA1467372855GCc.1034+715A= (p.=)
n.918+715A=
c.1091+715A= (p.=)
4g.71756008C=CA1467372857GCc.1034+704G= (p.=)
n.918+704G=
c.1091+704G= (p.=)
4g.71756008C>TCA1467372858GCc.1034+704G>A (p.=)
n.918+704G>A
c.1091+704G>A (p.=)
4g.71756011A=CA1467372859GCc.1034+701T= (p.=)
n.918+701T=
c.1091+701T= (p.=)
4g.71756011A>CCA99065333GCc.1034+701T>G (p.=)
n.918+701T>G
c.1091+701T>G (p.=)
dbSNP gnomAD
4g.71756012_71756013delinsCTCA1467372860GCc.1034+699_1034+700delinsAG (p.=)
n.918+699_918+700delinsAG
c.1091+699_1091+700delinsAG (p.=)
4g.71756013T>ACA1467372863GCc.1034+699A>T (p.=)
n.918+699A>T
c.1091+699A>T (p.=)
4g.71756013T=CA1467372862GCc.1034+699A= (p.=)
n.918+699A=
c.1091+699A= (p.=)
4g.71756020dupCA1467372861GCc.1034+699dup (p.=)
n.918+699dup
c.1091+699dup (p.=)
dbSNP
4g.71756020delCA798110449GCc.1034+699del (p.=)
n.918+699del
c.1091+699del (p.=)
dbSNP
4g.71756014T>CCA99065338GCc.1034+698A>G (p.=)
n.918+698A>G
c.1091+698A>G (p.=)
dbSNP gnomAD
4g.71756014T=CA1467372864GCc.1034+698A= (p.=)
n.918+698A=
c.1091+698A= (p.=)
4g.71756017T>ACA1063992475GCc.1034+695A>T (p.=)
n.918+695A>T
c.1091+695A>T (p.=)
4g.71756017T>CCA1467372866GCc.1034+695A>G (p.=)
n.918+695A>G
c.1091+695A>G (p.=)
4g.71756017T=CA1467372865GCc.1034+695A= (p.=)
n.918+695A=
c.1091+695A= (p.=)
4g.71756022G>ACA99065346GCc.1034+690C>T (p.=)
n.918+690C>T
c.1091+690C>T (p.=)
dbSNP
4g.71756022G=CA1467372867GCc.1034+690C= (p.=)
n.918+690C=
c.1091+690C= (p.=)
4g.71756023T>GCA1467372869GCc.1034+689A>C (p.=)
n.918+689A>C
c.1091+689A>C (p.=)
4g.71756023T=CA1467372868GCc.1034+689A= (p.=)
n.918+689A=
c.1091+689A= (p.=)
4g.71756027A=CA1467372870GCc.1034+685T= (p.=)
n.918+685T=
c.1091+685T= (p.=)
4g.71756027A>TCA1467372871GCc.1034+685T>A (p.=)
n.918+685T>A
c.1091+685T>A (p.=)
4g.71756034A=CA1467372872GCc.1034+678T= (p.=)
n.918+678T=
c.1091+678T= (p.=)
4g.71756034A>GCA1467372873GCc.1034+678T>C (p.=)
n.918+678T>C
c.1091+678T>C (p.=)
4g.71756036G>ACA1467372874GCc.1034+676C>T (p.=)
n.918+676C>T
c.1091+676C>T (p.=)
4g.71756036G=CA1467372875GCc.1034+676C= (p.=)
n.918+676C=
c.1091+676C= (p.=)
4g.71756036G>TCA1063992480GCc.1034+676C>A (p.=)
n.918+676C>A
c.1091+676C>A (p.=)
4g.71756037A=CA1467372876GCc.1034+675T= (p.=)
n.918+675T=
c.1091+675T= (p.=)
4g.71756037A>GCA99065353GCc.1034+675T>C (p.=)
n.918+675T>C
c.1091+675T>C (p.=)
dbSNP

Number of alleles fetched