Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.53056891C>ACA2572490199c.318-9652G>T
c.465-13637G>T
c.447+20797G>T
3g.53056891C=CA1365145570c.318-9652G=
c.465-13637G=
c.447+20797G=
3g.53056891C>TCA74805239c.318-9652G>A
c.465-13637G>A
c.447+20797G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.53056892A=CA1365145571c.318-9653T=
c.465-13638T=
c.447+20796T=
3g.53056892A>GCA1365145572c.318-9653T>C
c.465-13638T>C
c.447+20796T>C
dbSNP
3g.53056893A>GCA2502977287c.318-9654T>C
c.465-13639T>C
c.447+20795T>C
3g.53056897C=CA1365145573c.318-9658G=
c.465-13643G=
c.447+20791G=
3g.53056897C>GCA1048013651c.318-9658G>C
c.465-13643G>C
c.447+20791G>C
dbSNP gnomAD v3 gnomAD v4
3g.53056898T>CCA2597569091c.318-9659A>G
c.465-13644A>G
c.447+20790A>G
dbSNP gnomAD v3 gnomAD v4
3g.53056904G=CA1365145574c.318-9665C=
c.465-13650C=
c.447+20784C=
3g.53056906_53056935dupCA908188321c.318-9695_318-9666dup
c.465-13680_465-13651dup
c.447+20754_447+20783dup
dbSNP
3g.53056908T>GCA1048013652c.318-9669A>C
c.465-13654A>C
c.447+20780A>C
dbSNP gnomAD v3 gnomAD v4
3g.53056908T=CA1365145575c.318-9669A=
c.465-13654A=
c.447+20780A=
3g.53056912T>CCA74805242c.318-9673A>G
c.465-13658A>G
c.447+20776A>G
dbSNP
3g.53056912T=CA1365145576c.318-9673A=
c.465-13658A=
c.447+20776A=
3g.53056913G>ACA542918786c.318-9674C>T
c.465-13659C>T
c.447+20775C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.53056913G=CA1365145577c.318-9674C=
c.465-13659C=
c.447+20775C=
3g.53056920T>CCA2526204360c.318-9681A>G
c.465-13666A>G
c.447+20768A>G
3g.53056924A=CA1365145578c.318-9685T=
c.465-13670T=
c.447+20764T=
3g.53056924A>CCA2756287196c.318-9685T>G
c.465-13670T>G
c.447+20764T>G
3g.53056924A>GCA1365145579c.318-9685T>C
c.465-13670T>C
c.447+20764T>C
dbSNP
3g.53056925G>ACA74805256c.318-9686C>T
c.465-13671C>T
c.447+20763C>T
dbSNP
3g.53056925G=CA1365145580c.318-9686C=
c.465-13671C=
c.447+20763C=
3g.53056926A=CA1365145581c.318-9687T=
c.465-13672T=
c.447+20762T=
3g.53056926A>GCA908188330c.318-9687T>C
c.465-13672T>C
c.447+20762T>C
dbSNP gnomAD v3 gnomAD v4
3g.53056928G>ACA1365145582c.318-9689C>T
c.465-13674C>T
c.447+20760C>T
dbSNP
3g.53056928G=CA1365145583c.318-9689C=
c.465-13674C=
c.447+20760C=
3g.53056933C=CA1365145584c.318-9694G=
c.465-13679G=
c.447+20755G=
3g.53056933C>TCA908188331c.318-9694G>A
c.465-13679G>A
c.447+20755G>A
dbSNP gnomAD v3 gnomAD v4
3g.53056937G>CCA1365145586c.318-9698C>G
c.465-13683C>G
c.447+20751C>G
dbSNP
3g.53056937G=CA1365145585c.318-9698C=
c.465-13683C=
c.447+20751C=
3g.53056940A=CA1365145587c.318-9701T=
c.465-13686T=
c.447+20748T=
3g.53056940A>GCA1365145588c.318-9701T>C
c.465-13686T>C
c.447+20748T>C
dbSNP
3g.53056944C>ACA908188332c.318-9705G>T
c.465-13690G>T
c.447+20744G>T
dbSNP
3g.53056944C=CA1365145589c.318-9705G=
c.465-13690G=
c.447+20744G=
3g.53056947_53056951delinsGTGTTCA1365145590c.318-9712_318-9708delinsAACAC
c.465-13697_465-13693delinsAACAC
c.447+20737_447+20741delinsAACAC
3g.53056948T>CCA1365145591c.318-9709A>G
c.465-13694A>G
c.447+20740A>G
dbSNP
3g.53056948T=CA1365145592c.318-9709A=
c.465-13694A=
c.447+20740A=
3g.53056954_53056957delCA908188340c.318-9712_318-9709del
c.465-13697_465-13694del
c.447+20737_447+20740del
dbSNP gnomAD v3 gnomAD v4
3g.53056951T>GCA1365145594c.318-9712A>C
c.465-13697A>C
c.447+20737A>C
dbSNP
3g.53056951T=CA1365145593c.318-9712A=
c.465-13697A=
c.447+20737A=
3g.53056955T>CCA1048013658c.318-9716A>G
c.465-13701A>G
c.447+20733A>G
dbSNP gnomAD v3 gnomAD v4
3g.53056955T=CA1365145595c.318-9716A=
c.465-13701A=
c.447+20733A=
3g.53056968C=CA1365145596c.318-9729G=
c.465-13714G=
c.447+20720G=
3g.53056968C>TCA1365145597c.318-9729G>A
c.465-13714G>A
c.447+20720G>A
dbSNP
3g.53056970G>ACA542918787c.318-9731C>T
c.465-13716C>T
c.447+20718C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.53056970G=CA1365145598c.318-9731C=
c.465-13716C=
c.447+20718C=
3g.53056970G>TCA2570708272c.318-9731C>A
c.465-13716C>A
c.447+20718C>A
3g.53056975A=CA1365145599c.318-9736T=
c.465-13721T=
c.447+20713T=
3g.53056975A>GCA1048013661c.318-9736T>C
c.465-13721T>C
c.447+20713T>C
dbSNP gnomAD v3 gnomAD v4
3g.53056976G>CCA74805261c.318-9737C>G
c.465-13722C>G
c.447+20712C>G
dbSNP
3g.53056976G=CA1365145600c.318-9737C=
c.465-13722C=
c.447+20712C=
3g.53056976G>TCA908188341c.318-9737C>A
c.465-13722C>A
c.447+20712C>A
dbSNP
3g.53056977A=CA1365145601c.318-9738T=
c.465-13723T=
c.447+20711T=
3g.53056977A>GCA908188343c.318-9738T>C
c.465-13723T>C
c.447+20711T>C
dbSNP
3g.53056978G>ACA908188346c.318-9739C>T
c.465-13724C>T
c.447+20710C>T
dbSNP
3g.53056978G=CA1365145602c.318-9739C=
c.465-13724C=
c.447+20710C=
3g.53056981G=CA1365145603c.318-9742C=
c.465-13727C=
c.447+20707C=
3g.53056981G>TCA542918788c.318-9742C>A
c.465-13727C>A
c.447+20707C>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.53056984T>CCA908188352c.318-9745A>G
c.465-13730A>G
c.447+20704A>G
dbSNP
3g.53056984T=CA1365145604c.318-9745A=
c.465-13730A=
c.447+20704A=
3g.53056985A=CA1365145606c.318-9746T=
c.465-13731T=
c.447+20703T=
3g.53056985A>GCA1048013664c.318-9746T>C
c.465-13731T>C
c.447+20703T>C
dbSNP gnomAD v3 gnomAD v4
3g.53056985_53056986delinsACCA1365145605c.318-9747_318-9746delinsGT
c.465-13732_465-13731delinsGT
c.447+20702_447+20703delinsGT
3g.53056986delCA542918789c.318-9747del
c.465-13732del
c.447+20702del
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.53056986C>ACA1365145608c.318-9747G>T
c.465-13732G>T
c.447+20702G>T
dbSNP
3g.53056986C=CA1365145607c.318-9747G=
c.465-13732G=
c.447+20702G=
3g.53056987T>ACA542918790c.318-9748A>T
c.465-13733A>T
c.447+20701A>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.53056987T=CA1365145609c.318-9748A=
c.465-13733A=
c.447+20701A=
3g.53056988T>GCA908188380c.318-9749A>C
c.465-13734A>C
c.447+20700A>C
dbSNP
3g.53056988T=CA1365145610c.318-9749A=
c.465-13734A=
c.447+20700A=

Number of alleles fetched