Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129532211G>ACA546228465RHOc.531-40G>A (n.531-40G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129532211G>CCA2667616680RHOc.531-40G>C (n.531-40G>C)
gnomAD v4
3g.129532211G=CA1401210768RHOc.531-40G= (n.531-40G=)
3g.129532212T>ACA2667616683RHOc.531-39T>A (n.531-39T>A)
gnomAD v4
3g.129532213C>ACA2667616685RHOc.531-38C>A (n.531-38C>A)
gnomAD v4
3g.129532214C>ACA2667616686RHOc.531-37C>A (n.531-37C>A)
gnomAD v4
3g.129532215C>ACA2577961787RHOc.531-36C>A (n.531-36C>A)
gnomAD v4
3g.129532215C=CA1401210772RHOc.531-36C= (n.531-36C=)
3g.129532215C>TCA2607197RHOc.531-36C>T (n.531-36C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532219C>ACA2607198RHOc.531-32C>A (n.531-32C>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532219C=CA1401210776RHOc.531-32C= (n.531-32C=)
3g.129532219C>TCA82649749RHOc.531-32C>T (n.531-32C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129532222G>ACA1401210779RHOc.531-29G>A (n.531-29G>A)
dbSNP
3g.129532222G=CA1401210778RHOc.531-29G= (n.531-29G=)
3g.129532223C=CA1401210781RHOc.531-28C= (n.531-28C=)
3g.129532223C>GCA898752962RHOc.531-28C>G (n.531-28C>G)
dbSNP gnomAD v4
3g.129532223C>TCA82649753RHOc.531-28C>T (n.531-28C>T)
dbSNP
3g.129532224A=CA1401210786RHOc.531-27A= (n.531-27A=)
3g.129532224A>GCA1401210787RHOc.531-27A>G (n.531-27A>G)
dbSNP gnomAD v4
3g.129532225G>ACA2607199RHOc.531-26G>A (n.531-26G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532225G=CA1401210789RHOc.531-26G= (n.531-26G=)
3g.129532226G>ACA546228470RHOc.531-25G>A (n.531-25G>A)
dbSNP gnomAD v2 gnomAD v4
3g.129532226G>CCA2667616696RHOc.531-25G>C (n.531-25G>C)
gnomAD v4
3g.129532226G=CA1401210791RHOc.531-25G= (n.531-25G=)
3g.129532227G>ACA2667616700RHOc.531-24G>A (n.531-24G>A)
gnomAD v4
3g.129532227G=CA1401210793RHOc.531-24G= (n.531-24G=)
3g.129532227G>TCA546228471RHOc.531-24G>T (n.531-24G>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129532228T>ACA2577961788RHOc.531-23T>A (n.531-23T>A)
3g.129532228T>GCA1401210796RHOc.531-23T>G (n.531-23T>G)
dbSNP
3g.129532228T=CA1401210795RHOc.531-23T= (n.531-23T=)
3g.129532228_129532234delCA2533051453RHOc.531-23_531-17del (n.531-23_531-17del)
dbSNP
3g.129532229C>ACA1053436379RHOc.531-22C>A (n.531-22C>A)
dbSNP gnomAD v3 gnomAD v4
3g.129532229C=CA1401210798RHOc.531-22C= (n.531-22C=)
3g.129532229C>GCA546228473RHOc.531-22C>G (n.531-22C>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129532229C>TCA2667616706RHOc.531-22C>T (n.531-22C>T)
gnomAD v4
3g.129532230T>CCA1401210801RHOc.531-21T>C (n.531-21T>C)
dbSNP
3g.129532230T=CA1401210800RHOc.531-21T= (n.531-21T=)
3g.129532231C=CA1401210804RHOc.531-20C= (n.531-20C=)
3g.129532231C>GCA2607200RHOc.531-20C>G (n.531-20C>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532232C>TCA2667616708RHOc.531-19C>T (n.531-19C>T)
gnomAD v4
3g.129532233C=CA1401210807RHOc.531-18C= (n.531-18C=)
3g.129532233C>TCA1401210808RHOc.531-18C>T (n.531-18C>T)
dbSNP gnomAD v4
3g.129532235A=CA1401210810RHOc.531-16A= (n.531-16A=)
3g.129532235A>CCA1401210811RHOc.531-16A>C (n.531-16A>C)
dbSNP
3g.129532235A>GCA1401210812RHOc.531-16A>G (n.531-16A>G)
dbSNP
3g.129532235_129532236insGACCA2569247469RHOc.531-16_531-15insGAC (n.531-16_531-15insGAC)
dbSNP
3g.129532236C>ACA546228476RHOc.531-15C>A (n.531-15C>A)
dbSNP gnomAD v2 gnomAD v4
3g.129532236C=CA1401210815RHOc.531-15C= (n.531-15C=)
3g.129532236C>TCA2607201RHOc.531-15C>T (n.531-15C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532239G>ACA2607202RHOc.531-12G>A (n.531-12G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532239G=CA1401210821RHOc.531-12G= (n.531-12G=)
3g.129532240C=CA1401210824RHOc.531-11C= (n.531-11C=)
3g.129532240C>TCA546228482RHOc.531-11C>T (n.531-11C>T)
dbSNP gnomAD v2 gnomAD v4
3g.129532241C>ACA2758364192RHOc.531-10C>A (n.531-10C>A)
3g.129532241C>TCA2577961789RHOc.531-10C>T (n.531-10C>T)
gnomAD v4
3g.129532242T>CCA2758364193RHOc.531-9T>C (n.531-9T>C)
3g.129532243G>CCA2577961790RHOc.531-8G>C (n.531-8G>C)
gnomAD v4
3g.129532244T>CCA1401210826RHOc.531-7T>C (n.531-7T>C)
dbSNP
3g.129532244T=CA1401210825RHOc.531-7T= (n.531-7T=)
3g.129532248C>GCA2667616712RHOc.531-3C>G (n.531-3C>G)
gnomAD v4
3g.129532248C>TCA2667616718RHOc.531-3C>T (n.531-3C>T)
gnomAD v4
3g.129532249A>CCA354499040RHOc.531-2A>C (n.531-2A>C)
3g.129532249A>GCA354499043RHOc.531-2A>G (n.531-2A>G)
ClinVar
3g.129532249A>TCA354499046RHOc.531-2A>T (n.531-2A>T)
3g.129532250G>ACA354499049RHOc.531-1G>A (n.531-1G>A)
3g.129532250G>CCA354499051RHOc.531-1G>C (n.531-1G>C)
3g.129532250G>TCA354499050RHOc.531-1G>T (n.531-1G>T)
3g.129532251G>ACA435644623RHOc.531G>A (p.Arg177=)
gnomAD v4
3g.129532251G>CCA354499052RHOc.531G>C (p.Arg177Ser)
3g.129532251G>TCA354499053RHOc.531G>T (p.Arg177Ser)
3g.129532252T>ACA354499055RHOc.532T>A (p.Tyr178Asn)
3g.129532252T>CCA354499057RHOc.532T>C (p.Tyr178His)
ClinVar dbSNP
3g.129532252T>GCA354499061RHOc.532T>G (p.Tyr178Asp)
3g.129532252T=CA1401210834RHOc.532T= (p.Tyr178=)
3g.129532253A=CA1401210844RHOc.533A= (p.Tyr178=)
3g.129532253A>CCA354499065RHOc.533A>C (p.Tyr178Ser)
3g.129532253A>GCA256672RHOc.533A>G (p.Tyr178Cys)
ClinVar dbSNP gnomAD v4
3g.129532253A>TCA354499072RHOc.533A>T (p.Tyr178Phe)
3g.129532254C>ACA354499076RHOc.534C>A (p.Tyr178Ter)
3g.129532254C>GCA354499079RHOc.534C>G (p.Tyr178Ter)
3g.129532254C>TCA435644630RHOc.534C>T (p.Tyr178=)
3g.129532255A>CCA354499081RHOc.535A>C (p.Ile179Leu)
3g.129532255A>GCA354499083RHOc.535A>G (p.Ile179Val)
3g.129532255A>TCA354499085RHOc.535A>T (p.Ile179Phe)
3g.129532256T>ACA354499087RHOc.536T>A (p.Ile179Asn)
ClinVar
3g.129532256T>CCA354499094RHOc.536T>C (p.Ile179Thr)
gnomAD v4
3g.129532256T>GCA354499092RHOc.536T>G (p.Ile179Ser)
3g.129532256_129532257delinsTCCA1401210855RHOc.536_537delinsTC (p.Ile179=)
3g.129532257C>ACA435644634RHOc.537C>A (p.Ile179=)
3g.129532257C>GCA354499095RHOc.537C>G (p.Ile179Met)
3g.129532257C>TCA435644636RHOc.537C>T (p.Ile179=)
3g.129532260delCA898753006RHOc.540del (p.Glu181ArgfsTer?)
ClinVar dbSNP
3g.129532258C>ACA354499098RHOc.538C>A (p.Pro180Thr)
ClinVar dbSNP
3g.129532258C=CA1401210870RHOc.538C= (p.Pro180=)
3g.129532258C>GCA354499102RHOc.538C>G (p.Pro180Ala)
ClinVar dbSNP
3g.129532258C>TCA354499107RHOc.538C>T (p.Pro180Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.129532259C>ACA354499113RHOc.539C>A (p.Pro180His)
3g.129532259C=CA1401210885RHOc.539C= (p.Pro180=)
3g.129532259C>GCA354499115RHOc.539C>G (p.Pro180Arg)
ClinVar dbSNP
3g.129532259C>TCA354499117RHOc.539C>T (p.Pro180Leu)
ClinVar dbSNP
3g.129532260C>ACA435644638RHOc.540C>A (p.Pro180=)
3g.129532260C=CA1401210888RHOc.540C= (p.Pro180=)
3g.129532260C>GCA435644639RHOc.540C>G (p.Pro180=)
gnomAD v4
3g.129532260C>TCA2607203RHOc.540C>T (p.Pro180=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129532261G>ACA275168RHOc.541G>A (p.Glu181Lys)
ClinVar dbSNP COSMIC
3g.129532261G>CCA2607204RHOc.541G>C (p.Glu181Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532261G=CA1401210897RHOc.541G= (p.Glu181=)
3g.129532261G>TCA354499124RHOc.541G>T (p.Glu181Ter)
3g.129532262A>CCA354499130RHOc.542A>C (p.Glu181Ala)
3g.129532262A>GCA354499127RHOc.542A>G (p.Glu181Gly)
3g.129532262A>TCA354499126RHOc.542A>T (p.Glu181Val)
3g.129532263G>ACA435644643RHOc.543G>A (p.Glu181=)
3g.129532263G>CCA354499137RHOc.543G>C (p.Glu181Asp)
3g.129532263G>TCA354499135RHOc.543G>T (p.Glu181Asp)
3g.129532264G>ACA256679RHOc.544G>A (p.Gly182Ser)
ClinVar dbSNP
3g.129532264G>CCA354499141RHOc.544G>C (p.Gly182Arg)
3g.129532264G=CA1401210908RHOc.544G= (p.Gly182=)
3g.129532264G>TCA354499145RHOc.544G>T (p.Gly182Cys)
3g.129532265G>ACA354499146RHOc.545G>A (p.Gly182Asp)
ClinVar dbSNP
3g.129532265G>CCA354499151RHOc.545G>C (p.Gly182Ala)
3g.129532265G=CA1401210916RHOc.545G= (p.Gly182=)
3g.129532265G>TCA354499148RHOc.545G>T (p.Gly182Val)
ClinVar dbSNP
3g.129532265_129532266delinsAACA1139655827RHOc.545_546delinsAA (p.Gly182Glu)
ClinVar dbSNP
3g.129532265_129532266delinsGCCA1401210919RHOc.545_546delinsGC (p.Gly182=)
3g.129532266C>ACA435644645RHOc.546C>A (p.Gly182=)
3g.129532266C=CA1401210929RHOc.546C= (p.Gly182=)
3g.129532266C>GCA435644646RHOc.546C>G (p.Gly182=)
3g.129532266C>TCA435644647RHOc.546C>T (p.Gly182=)
ClinVar dbSNP gnomAD v4 COSMIC
3g.129532267C>ACA354499154RHOc.547C>A (p.Leu183Met)
3g.129532267C>GCA354499162RHOc.547C>G (p.Leu183Val)
3g.129532267C>TCA435644648RHOc.547C>T (p.Leu183=)
3g.129532268_129532358dupCA915941573RHOc.548_638dup (p.Ile214AlafsTer?)
ClinVar dbSNP
3g.129532268T>ACA354499166RHOc.548T>A (p.Leu183Gln)
3g.129532268T>CCA354499170RHOc.548T>C (p.Leu183Pro)
3g.129532268T>GCA354499173RHOc.548T>G (p.Leu183Arg)
3g.129532268T=CA1401210941RHOc.548T= (p.Leu183=)
3g.129532269G>ACA435644652RHOc.549G>A (p.Leu183=)
3g.129532269G>CCA435644653RHOc.549G>C (p.Leu183=)
3g.129532269G>TCA435644654RHOc.549G>T (p.Leu183=)
3g.129532269dupCA891862902RHOc.549dup (p.Gln184AlafsTer?)
ClinVar dbSNP
3g.129532270C>ACA354499176RHOc.550C>A (p.Gln184Lys)
3g.129532270C>GCA354499180RHOc.550C>G (p.Gln184Glu)
3g.129532270C>TCA354499182RHOc.550C>T (p.Gln184Ter)
3g.129532271A=CA1401210951RHOc.551A= (p.Gln184=)
3g.129532271A>CCA354499185RHOc.551A>C (p.Gln184Pro)
3g.129532271A>GCA354499186RHOc.551A>G (p.Gln184Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129532271A>TCA354499187RHOc.551A>T (p.Gln184Leu)
3g.129532272G>ACA435644657RHOc.552G>A (p.Gln184=)
3g.129532272G>CCA354499191RHOc.552G>C (p.Gln184His)
3g.129532272G>TCA354499193RHOc.552G>T (p.Gln184His)
3g.129532273T>ACA354499201RHOc.553T>A (p.Cys185Ser)
3g.129532273T>CCA354499200RHOc.553T>C (p.Cys185Arg)
ClinVar dbSNP gnomAD v4
3g.129532273T>GCA354499198RHOc.553T>G (p.Cys185Gly)
3g.129532273T=CA1401210960RHOc.553T= (p.Cys185=)
3g.129532274G>ACA354499204RHOc.554G>A (p.Cys185Tyr)
ClinVar
3g.129532274G>CCA354499207RHOc.554G>C (p.Cys185Ser)
3g.129532274G>TCA354499210RHOc.554G>T (p.Cys185Phe)
gnomAD v4
3g.129532275C>ACA354499211RHOc.555C>A (p.Cys185Ter)
3g.129532275C>GCA354499212RHOc.555C>G (p.Cys185Trp)
3g.129532275C>TCA435644666RHOc.555C>T (p.Cys185=)
gnomAD v4
3g.129532276T>ACA354499213RHOc.556T>A (p.Ser186Thr)
3g.129532276T>CCA354499214RHOc.556T>C (p.Ser186Pro)
ClinVar
3g.129532276T>GCA354499216RHOc.556T>G (p.Ser186Ala)
3g.129532277C>ACA354499219RHOc.557C>A (p.Ser186Ter)
3g.129532277C=CA1401210969RHOc.557C= (p.Ser186=)
3g.129532277C>GCA354499220RHOc.557C>G (p.Ser186Trp)
ClinVar dbSNP
3g.129532277C>TCA2607205RHOc.557C>T (p.Ser186Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
3g.129532278G>ACA2607206RHOc.558G>A (p.Ser186=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532278G>CCA435644683RHOc.558G>C (p.Ser186=)
3g.129532278G=CA1401210978RHOc.558G= (p.Ser186=)
3g.129532278G>TCA2607207RHOc.558G>T (p.Ser186=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532279T>ACA354499234RHOc.559T>A (p.Cys187Ser)
3g.129532279T>CCA354499233RHOc.559T>C (p.Cys187Arg)
ClinVar dbSNP
3g.129532279T>GCA354499230RHOc.559T>G (p.Cys187Gly)
3g.129532279T=CA1401210990RHOc.559T= (p.Cys187=)
3g.129532280G>ACA354499244RHOc.560G>A (p.Cys187Tyr)
ClinVar dbSNP COSMIC
3g.129532280G>CCA354499239RHOc.560G>C (p.Cys187Ser)
ClinVar dbSNP
3g.129532280G=CA1401210998RHOc.560G= (p.Cys187=)
3g.129532280G>TCA354499242RHOc.560G>T (p.Cys187Phe)
ClinVar dbSNP
3g.129532281T>ACA354499248RHOc.561T>A (p.Cys187Ter)
3g.129532281T>CCA435644698RHOc.561T>C (p.Cys187=)
3g.129532281T>GCA354499251RHOc.561T>G (p.Cys187Trp)
3g.129532282G>ACA270025RHOc.562G>A (p.Gly188Arg)
ClinVar dbSNP COSMIC
3g.129532282G>CCA354499264RHOc.562G>C (p.Gly188Arg)
3g.129532282G=CA1401211010RHOc.562G= (p.Gly188=)
3g.129532282G>TCA354499268RHOc.562G>T (p.Gly188Ter)
3g.129532283G>ACA354499271RHOc.563G>A (p.Gly188Glu)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.129532283G>CCA354499274RHOc.563G>C (p.Gly188Ala)
3g.129532283G=CA1401211016RHOc.563G= (p.Gly188=)
3g.129532283G>TCA354499278RHOc.563G>T (p.Gly188Val)
3g.129532284A>CCA435644717RHOc.564A>C (p.Gly188=)
3g.129532284A>GCA435644719RHOc.564A>G (p.Gly188=)
3g.129532284A>TCA435644722RHOc.564A>T (p.Gly188=)
3g.129532285A>CCA354499281RHOc.565A>C (p.Ile189Leu)
3g.129532285A>GCA354499284RHOc.565A>G (p.Ile189Val)
3g.129532285A>TCA354499286RHOc.565A>T (p.Ile189Phe)
3g.129532286T>ACA354499293RHOc.566T>A (p.Ile189Asn)
3g.129532286T>CCA354499289RHOc.566T>C (p.Ile189Thr)
3g.129532286T>GCA354499291RHOc.566T>G (p.Ile189Ser)
3g.129532287C>ACA435644739RHOc.567C>A (p.Ile189=)
3g.129532287C=CA1401211019RHOc.567C= (p.Ile189=)
3g.129532287C>GCA354499296RHOc.567C>G (p.Ile189Met)
3g.129532287C>TCA2607208RHOc.567C>T (p.Ile189=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532288G>ACA256670RHOc.568G>A (p.Asp190Asn)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.129532288G>CCA354499304RHOc.568G>C (p.Asp190His)
ClinVar dbSNP
3g.129532288G=CA1401211029RHOc.568G= (p.Asp190=)
3g.129532288G>TCA256684RHOc.568G>T (p.Asp190Tyr)
ClinVar dbSNP gnomAD v4
3g.129532289A=CA1401211041RHOc.569A= (p.Asp190=)
3g.129532289A>CCA354499308RHOc.569A>C (p.Asp190Ala)
3g.129532289A>GCA256673RHOc.569A>G (p.Asp190Gly)
ClinVar dbSNP
3g.129532289A>TCA354499312RHOc.569A>T (p.Asp190Val)
3g.129532290C>ACA354499314RHOc.570C>A (p.Asp190Glu)
3g.129532290C=CA1401211050RHOc.570C= (p.Asp190=)
3g.129532290C>GCA354499320RHOc.570C>G (p.Asp190Glu)
ClinVar dbSNP
3g.129532290C>TCA435644762RHOc.570C>T (p.Asp190=)
3g.129532291T>ACA354499324RHOc.571T>A (p.Tyr191Asn)
ClinVar dbSNP
3g.129532291T>CCA354499328RHOc.571T>C (p.Tyr191His)
3g.129532291T>GCA354499331RHOc.571T>G (p.Tyr191Asp)
ClinVar dbSNP
3g.129532291T=CA1401211059RHOc.571T= (p.Tyr191=)
3g.129532292A>CCA354469676RHOc.572A>C (p.Tyr191Ser)
3g.129532292A>GCA354469678RHOc.572A>G (p.Tyr191Cys)
3g.129532292A>TCA354469675RHOc.572A>T (p.Tyr191Phe)
gnomAD v4
3g.129532293C>ACA354469680RHOc.573C>A (p.Tyr191Ter)
3g.129532293C>GCA354469682RHOc.573C>G (p.Tyr191Ter)
3g.129532293C>TCA435768906RHOc.573C>T (p.Tyr191=)
COSMIC
3g.129532294T>ACA354469683RHOc.574T>A (p.Tyr192Asn)
gnomAD v4
3g.129532294T>CCA354469684RHOc.574T>C (p.Tyr192His)
3g.129532294T>GCA354469685RHOc.574T>G (p.Tyr192Asp)
3g.129532294dupCA2577961791RHOc.574dup (p.Tyr192LeufsTer?)
gnomAD v4
3g.129532295A=CA1401211071RHOc.575A= (p.Tyr192=)
3g.129532295A>CCA354469686RHOc.575A>C (p.Tyr192Ser)
3g.129532295A>GCA354469688RHOc.575A>G (p.Tyr192Cys)
dbSNP gnomAD v3 gnomAD v4
3g.129532295A>TCA354469690RHOc.575A>T (p.Tyr192Phe)
3g.129532296C>ACA354469691RHOc.576C>A (p.Tyr192Ter)
3g.129532296C=CA1401211074RHOc.576C= (p.Tyr192=)
3g.129532296C>GCA354469693RHOc.576C>G (p.Tyr192Ter)
3g.129532296C>TCA82620436RHOc.576C>T (p.Tyr192=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129532297A>CCA354469696RHOc.577A>C (p.Thr193Pro)
3g.129532297A>GCA354469697RHOc.577A>G (p.Thr193Ala)
3g.129532297A>TCA354469698RHOc.577A>T (p.Thr193Ser)
3g.129532298C>ACA2607210RHOc.578C>A (p.Thr193Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532298C=CA1401211083RHOc.578C= (p.Thr193=)
3g.129532298C>GCA354469702RHOc.578C>G (p.Thr193Arg)
3g.129532298C>TCA2607209RHOc.578C>T (p.Thr193Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532299G>ACA2607211RHOc.579G>A (p.Thr193=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532299G>CCA82620446RHOc.579G>C (p.Thr193=)
dbSNP gnomAD v3 gnomAD v4
3g.129532299G=CA1401211090RHOc.579G= (p.Thr193=)
3g.129532299G>TCA435768913RHOc.579G>T (p.Thr193=)
gnomAD v4
3g.129532300C>ACA354469705RHOc.580C>A (p.Leu194Ile)
3g.129532300C>GCA354469707RHOc.580C>G (p.Leu194Val)
3g.129532300C>TCA354469709RHOc.580C>T (p.Leu194Phe)
3g.129532301T>ACA354469711RHOc.581T>A (p.Leu194His)
3g.129532301T>CCA354469712RHOc.581T>C (p.Leu194Pro)
3g.129532301T>GCA354469714RHOc.581T>G (p.Leu194Arg)
3g.129532302C>ACA435768918RHOc.582C>A (p.Leu194=)
3g.129532302C=CA1401211094RHOc.582C= (p.Leu194=)
3g.129532302C>GCA435768920RHOc.582C>G (p.Leu194=)
dbSNP gnomAD v2 gnomAD v4
3g.129532302C>TCA435768921RHOc.582C>T (p.Leu194=)
gnomAD v4
3g.129532303A>CCA354469715RHOc.583A>C (p.Lys195Gln)
3g.129532303A>GCA354469717RHOc.583A>G (p.Lys195Glu)
3g.129532303A>TCA354469719RHOc.583A>T (p.Lys195Ter)
3g.129532304A>CCA354469720RHOc.584A>C (p.Lys195Thr)
3g.129532304A>GCA354469722RHOc.584A>G (p.Lys195Arg)
3g.129532304A>TCA354469724RHOc.584A>T (p.Lys195Met)
3g.129532305G>ACA435768926RHOc.585G>A (p.Lys195=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129532305G>CCA354469727RHOc.585G>C (p.Lys195Asn)
3g.129532305G=CA1401211097RHOc.585G= (p.Lys195=)
3g.129532305G>TCA354469726RHOc.585G>T (p.Lys195Asn)
dbSNP
3g.129532306C>ACA10615276RHOc.586C>A (p.Pro196Thr)
ClinVar dbSNP gnomAD v4
3g.129532306C=CA1401211103RHOc.586C= (p.Pro196=)
3g.129532306C>GCA354469730RHOc.586C>G (p.Pro196Ala)
3g.129532306C>TCA2607212RHOc.586C>T (p.Pro196Ser)
dbSNP ExAC gnomAD v4
3g.129532307C>ACA354469732RHOc.587C>A (p.Pro196Gln)
3g.129532307C=CA1401211109RHOc.587C= (p.Pro196=)
3g.129532307C>GCA354469734RHOc.587C>G (p.Pro196Arg)
3g.129532307C>TCA2607213RHOc.587C>T (p.Pro196Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532308G>ACA435768933RHOc.588G>A (p.Pro196=)
dbSNP gnomAD v2 gnomAD v4
3g.129532308G>CCA2607214RHOc.588G>C (p.Pro196=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532308G=CA1401211112RHOc.588G= (p.Pro196=)
3g.129532308G>TCA435768934RHOc.588G>T (p.Pro196=)
dbSNP
3g.129532309G>ACA354469736RHOc.589G>A (p.Glu197Lys)
gnomAD v4
3g.129532309G>CCA354469737RHOc.589G>C (p.Glu197Gln)
dbSNP
3g.129532309G=CA1401211119RHOc.589G= (p.Glu197=)
3g.129532309G>TCA354469739RHOc.589G>T (p.Glu197Ter)
gnomAD v4
3g.129532310A>CCA354469741RHOc.590A>C (p.Glu197Ala)
3g.129532310A>GCA354469743RHOc.590A>G (p.Glu197Gly)
3g.129532310A>TCA354469744RHOc.590A>T (p.Glu197Val)
3g.129532311G>ACA435768939RHOc.591G>A (p.Glu197=)
3g.129532311G>CCA354469748RHOc.591G>C (p.Glu197Asp)
3g.129532311G>TCA354469746RHOc.591G>T (p.Glu197Asp)

Number of alleles fetched