Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.71755859T>CCA99065246GCc.1035-752A>G (p.=)
n.919-752A>G
c.1092-752A>G (p.=)
c.1034+853A>G (p.=)
dbSNP gnomAD
4g.71755859T=CA1467372804GCc.1035-752A= (p.=)
n.919-752A=
c.1092-752A= (p.=)
c.1034+853A= (p.=)
4g.71755868T>CCA798110407GCc.1035-761A>G (p.=)
n.919-761A>G
c.1092-761A>G (p.=)
c.1034+844A>G (p.=)
4g.71755868T=CA1467372805GCc.1035-761A= (p.=)
n.919-761A=
c.1092-761A= (p.=)
c.1034+844A= (p.=)
4g.71755870_71755872delinsTAACA1467372806GCc.1035-765_1035-763delinsTTA (p.=)
n.919-765_919-763delinsTTA
c.1092-765_1092-763delinsTTA (p.=)
c.1034+840_1034+842delinsTTA (p.=)
4g.71755871A=CA1467372807GCc.1035-764T= (p.=)
n.919-764T=
c.1092-764T= (p.=)
c.1034+841T= (p.=)
4g.71755871A>GCA99065258GCc.1035-764T>C (p.=)
n.919-764T>C
c.1092-764T>C (p.=)
c.1034+841T>C (p.=)
dbSNP gnomAD
4g.71755872_71755873delCA552290265GCc.1035-765_1035-764del (p.=)
n.919-765_919-764del
c.1092-765_1092-764del (p.=)
c.1034+840_1034+841del (p.=)
dbSNP gnomAD
4g.71755875T>ACA99065271GCc.1035-768A>T (p.=)
n.919-768A>T
c.1092-768A>T (p.=)
c.1034+837A>T (p.=)
dbSNP
4g.71755875T=CA1467372808GCc.1035-768A= (p.=)
n.919-768A=
c.1092-768A= (p.=)
c.1034+837A= (p.=)
4g.71755878C>ACA1063992423GCc.1035-771G>T (p.=)
n.919-771G>T
c.1092-771G>T (p.=)
c.1034+834G>T (p.=)
4g.71755878C=CA1467372809GCc.1035-771G= (p.=)
n.919-771G=
c.1092-771G= (p.=)
c.1034+834G= (p.=)
4g.71755878C>TCA1063992426GCc.1035-771G>A (p.=)
n.919-771G>A
c.1092-771G>A (p.=)
c.1034+834G>A (p.=)
4g.71755879A=CA1467372810GCc.1035-772T= (p.=)
n.919-772T=
c.1092-772T= (p.=)
c.1034+833T= (p.=)
4g.71755879A>TCA1467372811GCc.1035-772T>A (p.=)
n.919-772T>A
c.1092-772T>A (p.=)
c.1034+833T>A (p.=)
4g.71755880G>ACA1063992429GCc.1035-773C>T (p.=)
n.919-773C>T
c.1092-773C>T (p.=)
c.1034+832C>T (p.=)
4g.71755880G=CA1467372812GCc.1035-773C= (p.=)
n.919-773C=
c.1092-773C= (p.=)
c.1034+832C= (p.=)
4g.71755881T>GCA1467372814GCc.1035-774A>C (p.=)
n.919-774A>C
c.1092-774A>C (p.=)
c.1034+831A>C (p.=)
4g.71755881T=CA1467372813GCc.1035-774A= (p.=)
n.919-774A=
c.1092-774A= (p.=)
c.1034+831A= (p.=)
4g.71755882C>ACA1063992431GCc.1035-775G>T (p.=)
n.919-775G>T
c.1092-775G>T (p.=)
c.1034+830G>T (p.=)
4g.71755882C=CA1467372815GCc.1035-775G= (p.=)
n.919-775G=
c.1092-775G= (p.=)
c.1034+830G= (p.=)
4g.71755883C=CA1467372816GCc.1035-776G= (p.=)
n.919-776G=
c.1092-776G= (p.=)
c.1034+829G= (p.=)
4g.71755883C>GCA1467372817GCc.1035-776G>C (p.=)
n.919-776G>C
c.1092-776G>C (p.=)
c.1034+829G>C (p.=)
4g.71755885A=CA1467372818GCc.1035-778T= (p.=)
n.919-778T=
c.1092-778T= (p.=)
c.1034+827T= (p.=)
4g.71755885A>GCA99065276GCc.1035-778T>C (p.=)
n.919-778T>C
c.1092-778T>C (p.=)
c.1034+827T>C (p.=)
dbSNP
4g.71755886T>CCA1467372820GCc.1035-779A>G (p.=)
n.919-779A>G
c.1092-779A>G (p.=)
c.1034+826A>G (p.=)
4g.71755886T=CA1467372819GCc.1035-779A= (p.=)
n.919-779A=
c.1092-779A= (p.=)
c.1034+826A= (p.=)
4g.71755887G>ACA798110423GCc.1035-780C>T (p.=)
n.919-780C>T
c.1092-780C>T (p.=)
c.1034+825C>T (p.=)
4g.71755887G=CA1467372821GCc.1035-780C= (p.=)
n.919-780C=
c.1092-780C= (p.=)
c.1034+825C= (p.=)
4g.71755891C>ACA1063992434GCc.1035-784G>T (p.=)
n.919-784G>T
c.1092-784G>T (p.=)
c.1034+821G>T (p.=)
4g.71755891C=CA1467372822GCc.1035-784G= (p.=)
n.919-784G=
c.1092-784G= (p.=)
c.1034+821G= (p.=)
4g.71755895T>ACA1467372824GCc.1035-788A>T (p.=)
n.919-788A>T
c.1092-788A>T (p.=)
c.1034+817A>T (p.=)
4g.71755895T=CA1467372823GCc.1035-788A= (p.=)
n.919-788A=
c.1092-788A= (p.=)
c.1034+817A= (p.=)
4g.71755896A=CA1467372825GCc.1035-789T= (p.=)
n.919-789T=
c.1092-789T= (p.=)
c.1034+816T= (p.=)
4g.71755896A>CCA798110427GCc.1035-789T>G (p.=)
n.919-789T>G
c.1092-789T>G (p.=)
c.1034+816T>G (p.=)
4g.71755896A>GCA99065290GCc.1035-789T>C (p.=)
n.919-789T>C
c.1092-789T>C (p.=)
c.1034+816T>C (p.=)
dbSNP gnomAD
4g.71755911T>GCA99065294GCc.1034+801A>C (p.=)
n.918+801A>C
c.1091+801A>C (p.=)
dbSNP gnomAD
4g.71755911T=CA1467372826GCc.1034+801A= (p.=)
n.918+801A=
c.1091+801A= (p.=)
4g.71755914T>CCA552290266GCc.1034+798A>G (p.=)
n.918+798A>G
c.1091+798A>G (p.=)
gnomAD
4g.71755914T=CA1467372827GCc.1034+798A= (p.=)
n.918+798A=
c.1091+798A= (p.=)
4g.71755916G>ACA798110432GCc.1034+796C>T (p.=)
n.918+796C>T
c.1091+796C>T (p.=)
4g.71755916G=CA1467372828GCc.1034+796C= (p.=)
n.918+796C=
c.1091+796C= (p.=)
4g.71755924A=CA1467372829GCc.1034+788T= (p.=)
n.918+788T=
c.1091+788T= (p.=)
4g.71755924A>GCA552290267GCc.1034+788T>C (p.=)
n.918+788T>C
c.1091+788T>C (p.=)
gnomAD
4g.71755925A=CA1467372830GCc.1034+787T= (p.=)
n.918+787T=
c.1091+787T= (p.=)
4g.71755925A>GCA798110436GCc.1034+787T>C (p.=)
n.918+787T>C
c.1091+787T>C (p.=)
4g.71755925A>TCA1063992442GCc.1034+787T>A (p.=)
n.918+787T>A
c.1091+787T>A (p.=)
4g.71755926C=CA1467372831GCc.1034+786G= (p.=)
n.918+786G=
c.1091+786G= (p.=)
4g.71755926C>GCA552290268GCc.1034+786G>C (p.=)
n.918+786G>C
c.1091+786G>C (p.=)
gnomAD
4g.71755926C>TCA1063992447GCc.1034+786G>A (p.=)
n.918+786G>A
c.1091+786G>A (p.=)

Number of alleles fetched