Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.53057148C=CA1365145683c.318-9909G=
c.465-13894G=
c.447+20540G=
3g.53057148C>TCA11405231c.318-9909G>A
c.465-13894G>A
c.447+20540G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.53057151C=CA1365145684c.318-9912G=
c.465-13897G=
c.447+20537G=
3g.53057151C>TCA1365145685c.318-9912G>A
c.465-13897G>A
c.447+20537G>A
dbSNP gnomAD v3 gnomAD v4
3g.53057157A=CA1365145686c.318-9918T=
c.465-13903T=
c.447+20531T=
3g.53057157A>CCA1365145687c.318-9918T>G
c.465-13903T>G
c.447+20531T>G
dbSNP
3g.53057159T>CCA1048013724c.318-9920A>G
c.465-13905A>G
c.447+20529A>G
dbSNP gnomAD v3 gnomAD v4
3g.53057159T=CA1365145688c.318-9920A=
c.465-13905A=
c.447+20529A=
3g.53057164G>ACA2702645968c.318-9925C>T
c.465-13910C>T
c.447+20524C>T
dbSNP
3g.53057164G>TCA1048013725c.318-9925C>A
c.465-13910C>A
c.447+20524C>A
gnomAD v3 gnomAD v4
3g.53057165C=CA1365145689c.318-9926G=
c.465-13911G=
c.447+20523G=
3g.53057165C>TCA1048013726c.318-9926G>A
c.465-13911G>A
c.447+20523G>A
dbSNP gnomAD v3 gnomAD v4
3g.53057166A=CA1365145690c.318-9927T=
c.465-13912T=
c.447+20522T=
3g.53057166A>GCA908188468c.318-9927T>C
c.465-13912T>C
c.447+20522T>C
dbSNP gnomAD v3 gnomAD v4
3g.53057166A>TCA1048013728c.318-9927T>A
c.465-13912T>A
c.447+20522T>A
gnomAD v3 gnomAD v4
3g.53057167T>CCA1365145692c.318-9928A>G
c.465-13913A>G
c.447+20521A>G
dbSNP gnomAD v3 gnomAD v4
3g.53057167T=CA1365145691c.318-9928A=
c.465-13913A=
c.447+20521A=
3g.53057172A>TCA1048013729c.318-9933T>A
c.465-13918T>A
c.447+20516T>A
gnomAD v3 gnomAD v4
3g.53057172_53057173delinsAGCA1365145693c.318-9934_318-9933delinsCT
c.465-13919_465-13918delinsCT
c.447+20515_447+20516delinsCT
3g.53057173delCA916895550c.318-9934del
c.465-13919del
c.447+20515del
dbSNP gnomAD v3 gnomAD v4
3g.53057175A=CA1365145694c.318-9936T=
c.465-13921T=
c.447+20513T=
3g.53057175A>GCA1365145695c.318-9936T>C
c.465-13921T>C
c.447+20513T>C
dbSNP
3g.53057176G>ACA542918798c.318-9937C>T
c.465-13922C>T
c.447+20512C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.53057176G=CA1365145696c.318-9937C=
c.465-13922C=
c.447+20512C=
3g.53057178G=CA1365145697c.318-9939C=
c.465-13924C=
c.447+20510C=
3g.53057178G>TCA1048013730c.318-9939C>A
c.465-13924C>A
c.447+20510C>A
dbSNP gnomAD v3 gnomAD v4
3g.53057180C=CA1365145698c.318-9941G=
c.465-13926G=
c.447+20508G=
3g.53057180C>TCA74805317c.318-9941G>A
c.465-13926G>A
c.447+20508G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.53057181G>ACA74805319c.318-9942C>T
c.465-13927C>T
c.447+20507C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.53057181G=CA1365145699c.318-9942C=
c.465-13927C=
c.447+20507C=
3g.53057181G>TCA1365145700c.318-9942C>A
c.465-13927C>A
c.447+20507C>A
dbSNP
3g.53057183G=CA1365145701c.318-9944C=
c.465-13929C=
c.447+20505C=
3g.53057183G>TCA74805327c.318-9944C>A
c.465-13929C>A
c.447+20505C>A
dbSNP gnomAD v3 gnomAD v4
3g.53057184G=CA1365145702c.318-9945C=
c.465-13930C=
c.447+20504C=
3g.53057184G>TCA74805329c.318-9945C>A
c.465-13930C>A
c.447+20504C>A
dbSNP
3g.53057193C=CA1365145703c.318-9954G=
c.465-13939G=
c.447+20495G=
3g.53057193C>TCA542918799c.318-9954G>A
c.465-13939G>A
c.447+20495G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.53057194A=CA1365145704c.318-9955T=
c.465-13940T=
c.447+20494T=
3g.53057194A>CCA74805332c.318-9955T>G
c.465-13940T>G
c.447+20494T>G
dbSNP gnomAD v3 gnomAD v4
3g.53057194A>GCA2597569095c.318-9955T>C
c.465-13940T>C
c.447+20494T>C
dbSNP gnomAD v3 gnomAD v4
3g.53057194A>TCA542918800c.318-9955T>A
c.465-13940T>A
c.447+20494T>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.53057196_53057201delinsTGGCCACA1365145705c.318-9962_318-9957delinsTGGCCA
c.465-13947_465-13942delinsTGGCCA
c.447+20487_447+20492delinsTGGCCA
3g.53057197G>ACA2553146142c.318-9958C>T
c.465-13943C>T
c.447+20491C>T
3g.53057200_53057204delCA74805333c.318-9962_318-9958del
c.465-13947_465-13943del
c.447+20487_447+20491del
dbSNP
3g.53057198G>ACA74805336c.318-9959C>T
c.465-13944C>T
c.447+20490C>T
dbSNP
3g.53057198G=CA1365145706c.318-9959C=
c.465-13944C=
c.447+20490C=
3g.53057200C>ACA2597569096c.318-9961G>T
c.465-13946G>T
c.447+20488G>T
gnomAD v3 gnomAD v4
3g.53057200C>TCA2597569097c.318-9961G>A
c.465-13946G>A
c.447+20488G>A
dbSNP gnomAD v3 gnomAD v4
3g.53057201A=CA1365145707c.318-9962T=
c.465-13947T=
c.447+20487T=
3g.53057201A>GCA1365145708c.318-9962T>C
c.465-13947T>C
c.447+20487T>C
dbSNP

Number of alleles fetched