Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129529008C>ACA354496667RHOc.275C>A (p.Thr92Asn)
3g.129529008C>GCA354496669RHOc.275C>G (p.Thr92Ser)
3g.129529008C>TCA354496671RHOc.275C>T (p.Thr92Ile)
gnomAD v4
3g.129529009C>ACA435768740RHOc.276C>A (p.Thr92=)
3g.129529009C>GCA435768741RHOc.276C>G (p.Thr92=)
3g.129529009C>TCA435768742RHOc.276C>T (p.Thr92=)
gnomAD v4
3g.129529010A>CCA354496677RHOc.277A>C (p.Ser93Arg)
ClinVar
3g.129529010A>GCA354496676RHOc.277A>G (p.Ser93Gly)
3g.129529010A>TCA354496673RHOc.277A>T (p.Ser93Cys)
3g.129529011G>ACA354496680RHOc.278G>A (p.Ser93Asn)
3g.129529011G>CCA354496682RHOc.278G>C (p.Ser93Thr)
dbSNP
3g.129529011G>TCA354496685RHOc.278G>T (p.Ser93Ile)
3g.129529012C>ACA354496686RHOc.279C>A (p.Ser93Arg)
3g.129529012C=CA1401205933RHOc.279C= (p.Ser93=)
3g.129529012C>GCA354496688RHOc.279C>G (p.Ser93Arg)
ClinVar dbSNP gnomAD v4
3g.129529012C>TCA2607101RHOc.279C>T (p.Ser93=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129529013A>CCA354496690RHOc.280A>C (p.Thr94Pro)
3g.129529013A>GCA354496693RHOc.280A>G (p.Thr94Ala)
3g.129529013A>TCA354496695RHOc.280A>T (p.Thr94Ser)
3g.129529014C>ACA354496697RHOc.281C>A (p.Thr94Asn)
3g.129529014C=CA1401205954RHOc.281C= (p.Thr94=)
3g.129529014C>GCA354496699RHOc.281C>G (p.Thr94Ser)
3g.129529014C>TCA122825RHOc.281C>T (p.Thr94Ile)
ClinVar dbSNP
3g.129529015C>ACA435768745RHOc.282C>A (p.Thr94=)
3g.129529015C>GCA435768746RHOc.282C>G (p.Thr94=)
ClinVar
3g.129529015C>TCA435768747RHOc.282C>T (p.Thr94=)
3g.129529016C>ACA354496703RHOc.283C>A (p.Leu95Ile)
3g.129529016C>GCA354496702RHOc.283C>G (p.Leu95Val)
3g.129529016C>TCA354496701RHOc.283C>T (p.Leu95Phe)
3g.129529017T>ACA354496719RHOc.284T>A (p.Leu95His)
3g.129529017T>CCA354496712RHOc.284T>C (p.Leu95Pro)
ClinVar dbSNP
3g.129529017T>GCA354496718RHOc.284T>G (p.Leu95Arg)
3g.129529017T=CA1401205962RHOc.284T= (p.Leu95=)
3g.129529018C>ACA435768749RHOc.285C>A (p.Leu95=)
3g.129529018C>GCA435768750RHOc.285C>G (p.Leu95=)
ClinVar dbSNP
3g.129529018C>TCA435768751RHOc.285C>T (p.Leu95=)
3g.129529019T>ACA354496721RHOc.286T>A (p.Tyr96Asn)
3g.129529019T>CCA354496723RHOc.286T>C (p.Tyr96His)
3g.129529019T>GCA354496725RHOc.286T>G (p.Tyr96Asp)
3g.129529020A>CCA354496728RHOc.287A>C (p.Tyr96Ser)
3g.129529020A>GCA354496727RHOc.287A>G (p.Tyr96Cys)
3g.129529020A>TCA354496726RHOc.287A>T (p.Tyr96Phe)
3g.129529021C>ACA354496731RHOc.288C>A (p.Tyr96Ter)
3g.129529021C=CA1401205967RHOc.288C= (p.Tyr96=)
3g.129529021C>GCA354496732RHOc.288C>G (p.Tyr96Ter)
3g.129529021C>TCA2607102RHOc.288C>T (p.Tyr96=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529022A>CCA354496733RHOc.289A>C (p.Thr97Pro)
3g.129529022A>GCA354496734RHOc.289A>G (p.Thr97Ala)
3g.129529022A>TCA354496737RHOc.289A>T (p.Thr97Ser)
3g.129529023C>ACA354496739RHOc.290C>A (p.Thr97Asn)
dbSNP gnomAD v3 gnomAD v4
3g.129529023C=CA1401205977RHOc.290C= (p.Thr97=)
3g.129529023C>GCA354496742RHOc.290C>G (p.Thr97Ser)
3g.129529023C>TCA354496740RHOc.290C>T (p.Thr97Ile)
dbSNP gnomAD v3 gnomAD v4
3g.129529024C>ACA435768755RHOc.291C>A (p.Thr97=)
COSMIC
3g.129529024C>GCA435768756RHOc.291C>G (p.Thr97=)
3g.129529024C>TCA435768757RHOc.291C>T (p.Thr97=)
3g.129529025T>ACA354496744RHOc.292T>A (p.Ser98Thr)
3g.129529025T>CCA354496745RHOc.292T>C (p.Ser98Pro)
3g.129529025T>GCA354496751RHOc.292T>G (p.Ser98Ala)
3g.129529026C>ACA354496753RHOc.293C>A (p.Ser98Tyr)
3g.129529026C=CA1401205981RHOc.293C= (p.Ser98=)
3g.129529026C>GCA2607103RHOc.293C>G (p.Ser98Cys)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129529026C>TCA354496755RHOc.293C>T (p.Ser98Phe)
3g.129529027T>ACA435768760RHOc.294T>A (p.Ser98=)
dbSNP
3g.129529027T>CCA435768761RHOc.294T>C (p.Ser98=)
dbSNP
3g.129529027T>GCA435768762RHOc.294T>G (p.Ser98=)
3g.129529027T=CA1401205994RHOc.294T= (p.Ser98=)
3g.129529028C>ACA354496756RHOc.295C>A (p.Leu99Met)
3g.129529028C=CA1401205998RHOc.295C= (p.Leu99=)
3g.129529028C>GCA354496757RHOc.295C>G (p.Leu99Val)
3g.129529028C>TCA435768763RHOc.295C>T (p.Leu99=)
dbSNP gnomAD v4
3g.129529029T>ACA354496766RHOc.296T>A (p.Leu99Gln)
3g.129529029T>CCA354496768RHOc.296T>C (p.Leu99Pro)
ClinVar
3g.129529029T>GCA354496769RHOc.296T>G (p.Leu99Arg)
3g.129529030G>ACA435768764RHOc.297G>A (p.Leu99=)
3g.129529030G>CCA435768765RHOc.297G>C (p.Leu99=)
dbSNP
3g.129529030G>TCA435768766RHOc.297G>T (p.Leu99=)
3g.129529031C>ACA354496773RHOc.298C>A (p.His100Asn)
dbSNP gnomAD v2 gnomAD v4
3g.129529031C=CA1401206000RHOc.298C= (p.His100=)
3g.129529031C>GCA354496776RHOc.298C>G (p.His100Asp)
3g.129529031C>TCA354496771RHOc.298C>T (p.His100Tyr)
3g.129529032A=CA1401206004RHOc.299A= (p.His100=)
3g.129529032A>CCA354496779RHOc.299A>C (p.His100Pro)
ClinVar
3g.129529032A>GCA2607104RHOc.299A>G (p.His100Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529032A>TCA354496781RHOc.299A>T (p.His100Leu)
3g.129529033T>ACA354496784RHOc.300T>A (p.His100Gln)
3g.129529033T>CCA435768767RHOc.300T>C (p.His100=)
3g.129529033T>GCA354496787RHOc.300T>G (p.His100Gln)
3g.129529034G>ACA354496788RHOc.301G>A (p.Gly101Arg)
dbSNP gnomAD v2 gnomAD v4
3g.129529034G>CCA354496790RHOc.301G>C (p.Gly101Arg)
3g.129529034G=CA1401206009RHOc.301G= (p.Gly101=)
3g.129529034G>TCA354496792RHOc.301G>T (p.Gly101Ter)
3g.129529035G>ACA2607105RHOc.302G>A (p.Gly101Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129529035G>CCA354496797RHOc.302G>C (p.Gly101Ala)
gnomAD v4
3g.129529035G=CA1401206013RHOc.302G= (p.Gly101=)
3g.129529035G>TCA354496798RHOc.302G>T (p.Gly101Val)
ClinVar dbSNP
3g.129529036A>CCA435768768RHOc.303A>C (p.Gly101=)
dbSNP gnomAD v4
3g.129529036A>GCA435768769RHOc.303A>G (p.Gly101=)
3g.129529036A>TCA435768770RHOc.303A>T (p.Gly101=)
3g.129529037T>ACA354496800RHOc.304T>A (p.Tyr102Asn)
ClinVar dbSNP
3g.129529037T>CCA354496802RHOc.304T>C (p.Tyr102His)
dbSNP
3g.129529037T>GCA354496803RHOc.304T>G (p.Tyr102Asp)
3g.129529037T=CA1401206020RHOc.304T= (p.Tyr102=)
3g.129529038A>CCA354496809RHOc.305A>C (p.Tyr102Ser)
3g.129529038A>GCA354496807RHOc.305A>G (p.Tyr102Cys)
gnomAD v4
3g.129529038A>TCA354496805RHOc.305A>T (p.Tyr102Phe)
3g.129529039C>ACA354496810RHOc.306C>A (p.Tyr102Ter)
gnomAD v4
3g.129529039C=CA1401206026RHOc.306C= (p.Tyr102=)
3g.129529039C>GCA354496812RHOc.306C>G (p.Tyr102Ter)
ClinVar dbSNP
3g.129529039C>TCA435768772RHOc.306C>T (p.Tyr102=)
3g.129529040T>ACA354496816RHOc.307T>A (p.Phe103Ile)
3g.129529040T>CCA354496817RHOc.307T>C (p.Phe103Leu)
gnomAD v4
3g.129529040T>GCA82647042RHOc.307T>G (p.Phe103Val)
dbSNP
3g.129529040T=CA1401206031RHOc.307T= (p.Phe103=)
3g.129529041T>ACA354496821RHOc.308T>A (p.Phe103Tyr)
gnomAD v4
3g.129529041T>CCA354496823RHOc.308T>C (p.Phe103Ser)
3g.129529041T>GCA354496825RHOc.308T>G (p.Phe103Cys)
3g.129529042delCA2667615493RHOc.309del (p.Phe103LeufsTer?)
gnomAD v4
3g.129529042C>ACA354496826RHOc.309C>A (p.Phe103Leu)
3g.129529042C=CA1401206035RHOc.309C= (p.Phe103=)
3g.129529042C>GCA354496828RHOc.309C>G (p.Phe103Leu)
3g.129529042C>TCA2607106RHOc.309C>T (p.Phe103=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129529043G>ACA2607107RHOc.310G>A (p.Val104Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529043G>CCA354496835RHOc.310G>C (p.Val104Leu)
3g.129529043G=CA1401206040RHOc.310G= (p.Val104=)
3g.129529043G>TCA354496833RHOc.310G>T (p.Val104Phe)
3g.129529044T>ACA354496838RHOc.311T>A (p.Val104Asp)
3g.129529044T>CCA354496839RHOc.311T>C (p.Val104Ala)
gnomAD v4
3g.129529044T>GCA354496841RHOc.311T>G (p.Val104Gly)
3g.129529045C>ACA435768777RHOc.312C>A (p.Val104=)
3g.129529045C=CA1401206045RHOc.312C= (p.Val104=)
3g.129529045C>GCA435768779RHOc.312C>G (p.Val104=)
gnomAD v4
3g.129529045C>TCA2607108RHOc.312C>T (p.Val104=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129529046T>ACA354496843RHOc.313T>A (p.Phe105Ile)
3g.129529046T>CCA354496844RHOc.313T>C (p.Phe105Leu)
3g.129529046T>GCA354496846RHOc.313T>G (p.Phe105Val)
3g.129529047T>ACA354496849RHOc.314T>A (p.Phe105Tyr)
3g.129529047T>CCA354496851RHOc.314T>C (p.Phe105Ser)
3g.129529047T>GCA354496853RHOc.314T>G (p.Phe105Cys)
3g.129529048C>ACA354496855RHOc.315C>A (p.Phe105Leu)
3g.129529048C=CA1401206049RHOc.315C= (p.Phe105=)
3g.129529048C>GCA354496857RHOc.315C>G (p.Phe105Leu)
3g.129529048C>TCA2607109RHOc.315C>T (p.Phe105=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129529049G>ACA256683RHOc.316G>A (p.Gly106Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129529049G>CCA354496864RHOc.316G>C (p.Gly106Arg)
ClinVar dbSNP
3g.129529049G=CA1401206060RHOc.316G= (p.Gly106=)
3g.129529049G>TCA256669RHOc.316G>T (p.Gly106Trp)
ClinVar dbSNP
3g.129529050G>ACA354496865RHOc.317G>A (p.Gly106Glu)
3g.129529050G>CCA354496868RHOc.317G>C (p.Gly106Ala)
ClinVar dbSNP
3g.129529050G=CA1401206080RHOc.317G= (p.Gly106=)
3g.129529050G>TCA354496869RHOc.317G>T (p.Gly106Val)
ClinVar dbSNP
3g.129529051G>ACA435768785RHOc.318G>A (p.Gly106=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129529051G>CCA435768787RHOc.318G>C (p.Gly106=)
3g.129529051G=CA1401206085RHOc.318G= (p.Gly106=)
3g.129529051G>TCA435768788RHOc.318G>T (p.Gly106=)
dbSNP gnomAD v4
3g.129529052C>ACA354496870RHOc.319C>A (p.Pro107Thr)
3g.129529052C=CA1401206094RHOc.319C= (p.Pro107=)
3g.129529052C>GCA354496872RHOc.319C>G (p.Pro107Ala)
3g.129529052C>TCA354496873RHOc.319C>T (p.Pro107Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.129529054dupCA2667615538RHOc.321dup (p.Thr108HisfsTer15)
gnomAD v4
3g.129529053C>ACA2607110RHOc.320C>A (p.Pro107His)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129529053C=CA1401206099RHOc.320C= (p.Pro107=)
3g.129529053C>GCA354496878RHOc.320C>G (p.Pro107Arg)
3g.129529053C>TCA354496880RHOc.320C>T (p.Pro107Leu)
3g.129529054C>ACA2607111RHOc.321C>A (p.Pro107=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529054C=CA1401206111RHOc.321C= (p.Pro107=)
3g.129529054C>GCA435768792RHOc.321C>G (p.Pro107=)
3g.129529054C>TCA435768794RHOc.321C>T (p.Pro107=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129529055A=CA1401206122RHOc.322A= (p.Thr108=)
3g.129529055A>CCA354496888RHOc.322A>C (p.Thr108Pro)
dbSNP
3g.129529055A>GCA354496886RHOc.322A>G (p.Thr108Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.129529055A>TCA354496884RHOc.322A>T (p.Thr108Ser)
3g.129529055dupCA2607112RHOc.322dup (p.Thr108AsnfsTer15)
dbSNP ExAC gnomAD v2
3g.129529056C>ACA354496894RHOc.323C>A (p.Thr108Lys)
3g.129529056C=CA1401206130RHOc.323C= (p.Thr108=)
3g.129529056C>GCA354496892RHOc.323C>G (p.Thr108Arg)
3g.129529056C>TCA354496895RHOc.323C>T (p.Thr108Ile)
dbSNP gnomAD v3 gnomAD v4
3g.129529057A>CCA435768799RHOc.324A>C (p.Thr108=)
3g.129529057A>GCA435768801RHOc.324A>G (p.Thr108=)
3g.129529057A>TCA435768802RHOc.324A>T (p.Thr108=)
3g.129529058G>ACA354496896RHOc.325G>A (p.Gly109Arg)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.129529058G>CCA354496901RHOc.325G>C (p.Gly109Arg)
3g.129529058G=CA1401206139RHOc.325G= (p.Gly109=)
3g.129529058G>TCA354496898RHOc.325G>T (p.Gly109Ter)
dbSNP gnomAD v2 gnomAD v4
3g.129529059G>ACA354496904RHOc.326G>A (p.Gly109Glu)
3g.129529059G>CCA354496905RHOc.326G>C (p.Gly109Ala)
3g.129529059G>TCA354496907RHOc.326G>T (p.Gly109Val)
3g.129529060A>CCA435768807RHOc.327A>C (p.Gly109=)
dbSNP
3g.129529060A>GCA435768809RHOc.327A>G (p.Gly109=)
3g.129529060A>TCA435768810RHOc.327A>T (p.Gly109=)
3g.129529061T>ACA354496908RHOc.328T>A (p.Cys110Ser)
3g.129529061T>CCA354496911RHOc.328T>C (p.Cys110Arg)
ClinVar dbSNP gnomAD v4
3g.129529061T>GCA354496913RHOc.328T>G (p.Cys110Gly)
ClinVar dbSNP
3g.129529061T=CA1401206150RHOc.328T= (p.Cys110=)
3g.129529062G>ACA256681RHOc.329G>A (p.Cys110Tyr)
ClinVar dbSNP
3g.129529062G>CCA354496916RHOc.329G>C (p.Cys110Ser)
3g.129529062G=CA1401206162RHOc.329G= (p.Cys110=)
3g.129529062G>TCA354496917RHOc.329G>T (p.Cys110Phe)
ClinVar
3g.129529063C>ACA354496919RHOc.330C>A (p.Cys110Ter)
gnomAD v4
3g.129529063C>GCA354496922RHOc.330C>G (p.Cys110Trp)
ClinVar
3g.129529063C>TCA435768812RHOc.330C>T (p.Cys110=)
dbSNP gnomAD v4
3g.129529064A>CCA354496926RHOc.331A>C (p.Asn111His)
3g.129529064A>GCA354496925RHOc.331A>G (p.Asn111Asp)
3g.129529064A>TCA354496923RHOc.331A>T (p.Asn111Tyr)
3g.129529065A=CA1401206167RHOc.332A= (p.Asn111=)
3g.129529065A>CCA354496927RHOc.332A>C (p.Asn111Thr)
3g.129529065A>GCA2607113RHOc.332A>G (p.Asn111Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529065A>TCA354496928RHOc.332A>T (p.Asn111Ile)
3g.129529066T>ACA354496930RHOc.333T>A (p.Asn111Lys)
3g.129529066T>CCA435768816RHOc.333T>C (p.Asn111=)
3g.129529066T>GCA354496931RHOc.333T>G (p.Asn111Lys)
3g.129529067T>ACA354496932RHOc.334T>A (p.Leu112Met)
3g.129529067T>CCA435768817RHOc.334T>C (p.Leu112=)
dbSNP gnomAD v4
3g.129529067T>GCA354496933RHOc.334T>G (p.Leu112Val)
3g.129529068T>ACA354496934RHOc.335T>A (p.Leu112Ter)
3g.129529068T>CCA82647073RHOc.335T>C (p.Leu112Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129529068T>GCA354496935RHOc.335T>G (p.Leu112Trp)
3g.129529068T=CA1401206172RHOc.335T= (p.Leu112=)
3g.129529069G>ACA435768818RHOc.336G>A (p.Leu112=)
gnomAD v4
3g.129529069G>CCA354496937RHOc.336G>C (p.Leu112Phe)
dbSNP
3g.129529069G>TCA354496939RHOc.336G>T (p.Leu112Phe)
3g.129529070G>ACA354496945RHOc.337G>A (p.Glu113Lys)
ClinVar dbSNP
3g.129529070G>CCA354496942RHOc.337G>C (p.Glu113Gln)
3g.129529070G>TCA354496941RHOc.337G>T (p.Glu113Ter)
3g.129529071A>CCA354496947RHOc.338A>C (p.Glu113Ala)
3g.129529071A>GCA354496950RHOc.338A>G (p.Glu113Gly)
3g.129529071A>TCA354496953RHOc.338A>T (p.Glu113Val)
3g.129529072G>ACA435768823RHOc.339G>A (p.Glu113=)
3g.129529072G>CCA354496954RHOc.339G>C (p.Glu113Asp)
3g.129529072G>TCA354496957RHOc.339G>T (p.Glu113Asp)
3g.129529073G>ACA354496961RHOc.340G>A (p.Gly114Ser)
3g.129529073G>CCA354496959RHOc.340G>C (p.Gly114Arg)
3g.129529073G>TCA354496958RHOc.340G>T (p.Gly114Cys)
3g.129529074G>ACA256688RHOc.341G>A (p.Gly114Asp)
ClinVar dbSNP gnomAD v4
3g.129529074G>CCA2607114RHOc.341G>C (p.Gly114Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129529074G=CA1401206183RHOc.341G= (p.Gly114=)
3g.129529074G>TCA354496965RHOc.341G>T (p.Gly114Val)
ClinVar dbSNP
3g.129529075C>ACA435768827RHOc.342C>A (p.Gly114=)
3g.129529075C=CA1401206190RHOc.342C= (p.Gly114=)
3g.129529075C>GCA435768828RHOc.342C>G (p.Gly114=)
3g.129529075C>TCA435768829RHOc.342C>T (p.Gly114=)
dbSNP gnomAD v2 gnomAD v4
3g.129529076T>ACA354496967RHOc.343T>A (p.Phe115Ile)
3g.129529076T>CCA354496969RHOc.343T>C (p.Phe115Leu)
3g.129529076T>GCA354496970RHOc.343T>G (p.Phe115Val)
3g.129529077T>ACA354496971RHOc.344T>A (p.Phe115Tyr)
3g.129529077T>CCA354496976RHOc.344T>C (p.Phe115Ser)
3g.129529077T>GCA354496974RHOc.344T>G (p.Phe115Cys)
3g.129529078C>ACA354496979RHOc.345C>A (p.Phe115Leu)
3g.129529078C=CA1401206202RHOc.345C= (p.Phe115=)
3g.129529078C>GCA354496980RHOc.345C>G (p.Phe115Leu)
3g.129529078C>TCA435768833RHOc.345C>T (p.Phe115=)
dbSNP gnomAD v2 gnomAD v4
3g.129529079T>ACA354496981RHOc.346T>A (p.Phe116Ile)
3g.129529079T>CCA354496984RHOc.346T>C (p.Phe116Leu)
3g.129529079T>GCA354496985RHOc.346T>G (p.Phe116Val)
3g.129529080T>ACA2607115RHOc.347T>A (p.Phe116Tyr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529080T>CCA354496988RHOc.347T>C (p.Phe116Ser)
3g.129529080T>GCA354496991RHOc.347T>G (p.Phe116Cys)
3g.129529080T=CA1401206208RHOc.347T= (p.Phe116=)
3g.129529081T>ACA354496992RHOc.348T>A (p.Phe116Leu)
3g.129529081T>CCA435768835RHOc.348T>C (p.Phe116=)
3g.129529081T>GCA354496994RHOc.348T>G (p.Phe116Leu)
3g.129529082G>ACA354497001RHOc.349G>A (p.Ala117Thr)
3g.129529082G>CCA354496999RHOc.349G>C (p.Ala117Pro)
3g.129529082G>TCA354496996RHOc.349G>T (p.Ala117Ser)
3g.129529083C>ACA354497002RHOc.350C>A (p.Ala117Asp)
3g.129529083C>GCA354497003RHOc.350C>G (p.Ala117Gly)
3g.129529083C>TCA354497004RHOc.350C>T (p.Ala117Val)
gnomAD v4
3g.129529084C>ACA435768840RHOc.351C>A (p.Ala117=)
3g.129529084C=CA1401206219RHOc.351C= (p.Ala117=)
3g.129529084C>GCA435768841RHOc.351C>G (p.Ala117=)
3g.129529084C>TCA435768842RHOc.351C>T (p.Ala117=)
dbSNP gnomAD v2 gnomAD v4
3g.129529084_129529096delinsCACCCTGGGCGGTCA1401206216RHOc.351_361+2delinsCACCCTGGGCGGT
3g.129529085A>CCA354497007RHOc.352A>C (p.Thr118Pro)
3g.129529085A>GCA354497008RHOc.352A>G (p.Thr118Ala)
3g.129529085A>TCA354497009RHOc.352A>T (p.Thr118Ser)
3g.129529086_129529097delCA1139655816RHOc.353_361+3del
ClinVar dbSNP
3g.129529086C>ACA354497014RHOc.353C>A (p.Thr118Asn)
gnomAD v4
3g.129529086C>GCA354497013RHOc.353C>G (p.Thr118Ser)
3g.129529086C>TCA354497011RHOc.353C>T (p.Thr118Ile)
gnomAD v4 COSMIC
3g.129529086_129529087insACTTGGAGGTGAAATCGCCCTGTGGTCCA2704008115RHOc.353_354insACTTGGAGGTGAAATCGCCCTGTGGTC (p.Thr118_Leu119insLeuGlyGlyGluIleAlaLeuTrpSer)
dbSNP
3g.129529087C>ACA435768846RHOc.354C>A (p.Thr118=)
dbSNP gnomAD v4 COSMIC
3g.129529087C=CA1401206226RHOc.354C= (p.Thr118=)
3g.129529087C>GCA435768848RHOc.354C>G (p.Thr118=)
3g.129529087C>TCA435768849RHOc.354C>T (p.Thr118=)
3g.129529088C>ACA354497016RHOc.355C>A (p.Leu119Met)
COSMIC
3g.129529088C=CA1401206230RHOc.355C= (p.Leu119=)
3g.129529088C>GCA354497019RHOc.355C>G (p.Leu119Val)
ClinVar gnomAD v4
3g.129529088C>TCA2607116RHOc.355C>T (p.Leu119=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529089delCA2758363651RHOc.356del (p.Leu119ArgfsTer25)
3g.129529089T>ACA354497022RHOc.356T>A (p.Leu119Gln)
3g.129529089T>CCA354497023RHOc.356T>C (p.Leu119Pro)
3g.129529089T>GCA354497024RHOc.356T>G (p.Leu119Arg)
3g.129529089_129529090delinsTGCA1401206235RHOc.356_357delinsTG (p.Leu119=)
3g.129529090G>ACA435768850RHOc.357G>A (p.Leu119=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129529090G>CCA435768851RHOc.357G>C (p.Leu119=)
3g.129529090G=CA1401206248RHOc.357G= (p.Leu119=)
3g.129529090G>TCA435768853RHOc.357G>T (p.Leu119=)
gnomAD v4
3g.129529092delCA16042497RHOc.359del (p.Gly120AlafsTer24)
ClinVar dbSNP gnomAD v4
3g.129529091G>ACA354497028RHOc.358G>A (p.Gly120Ser)
gnomAD v4
3g.129529091G>CCA354497031RHOc.358G>C (p.Gly120Arg)
3g.129529091G=CA1401206258RHOc.358G= (p.Gly120=)
3g.129529091G>TCA354497030RHOc.358G>T (p.Gly120Cys)
dbSNP gnomAD v2 gnomAD v4
3g.129529092G>ACA2607117RHOc.359G>A (p.Gly120Asp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529092G>CCA82647107RHOc.359G>C (p.Gly120Ala)
dbSNP gnomAD v3 gnomAD v4
3g.129529092G=CA1401206262RHOc.359G= (p.Gly120=)
3g.129529092G>TCA354497037RHOc.359G>T (p.Gly120Val)
3g.129529093C>ACA2607118RHOc.360C>A (p.Gly120=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529093C=CA1401206267RHOc.360C= (p.Gly120=)
3g.129529093C>GCA435768857RHOc.360C>G (p.Gly120=)
dbSNP
3g.129529093C>TCA238621RHOc.360C>T (p.Gly120=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529094G>ACA2607119RHOc.361G>A (p.Gly121Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129529094G>CCA354497044RHOc.361G>C (p.Gly121Arg)
3g.129529094G=CA1401206277RHOc.361G= (p.Gly121=)
3g.129529094G>TCA354497045RHOc.361G>T (p.Gly121Cys)
gnomAD v4
3g.129529095G>ACA354497047RHOc.361+1G>A (n.361+1G>A)
ClinVar gnomAD v4
3g.129529095G>CCA354497053RHOc.361+1G>C (n.361+1G>C)
3g.129529095G>TCA354497059RHOc.361+1G>T (n.361+1G>T)
3g.129529096T>ACA354497061RHOc.361+2T>A (n.361+2T>A)
3g.129529096T>CCA354497065RHOc.361+2T>C (n.361+2T>C)
3g.129529096T>GCA354497064RHOc.361+2T>G (n.361+2T>G)
3g.129529099G>ACA1401206284RHOc.361+5G>A (n.361+5G>A)
ClinVar dbSNP gnomAD v4
3g.129529099G>CCA1401206283RHOc.361+5G>C (n.361+5G>C)
dbSNP
3g.129529099G=CA1401206285RHOc.361+5G= (n.361+5G=)
3g.129529099G>TCA2667615660RHOc.361+5G>T (n.361+5G>T)
gnomAD v4
3g.129529100A>CCA2758363658RHOc.361+6A>C (n.361+6A>C)
3g.129529101G>ACA2758363659RHOc.361+7G>A (n.361+7G>A)
3g.129529101G>TCA2667615661RHOc.361+7G>T (n.361+7G>T)
gnomAD v4
3g.129529101_129529102insACACA2758363664RHOc.361+7_361+8insACA (n.361+7_361+8insACA)
3g.129529102C=CA1401206286RHOc.361+8C= (n.361+8C=)
3g.129529102C>GCA2667615662RHOc.361+8C>G (n.361+8C>G)
gnomAD v4
3g.129529102C>TCA546417606RHOc.361+8C>T (n.361+8C>T)
dbSNP gnomAD v2
3g.129529103C=CA1401206296RHOc.361+9C= (n.361+9C=)
3g.129529103C>TCA2607121RHOc.361+9C>T (n.361+9C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529103_129529105delinsCGGCA1401206291RHOc.361+9_361+11delinsCGG (n.361+9_361+11delinsCGG)
3g.129529104G>ACA2607122RHOc.361+10G>A (n.361+10G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529104G>CCA1401206320RHOc.361+10G>C (n.361+10G>C)
dbSNP gnomAD v4
3g.129529104G=CA1401206316RHOc.361+10G= (n.361+10G=)
3g.129529104G>TCA82647132RHOc.361+10G>T (n.361+10G>T)
dbSNP gnomAD v4
3g.129529106delCA2607120RHOc.361+12del (n.361+12del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529105_129529106delCA1401206313RHOc.361+11_361+12del (n.361+11_361+12del)
dbSNP
3g.129529105G=CA1401206325RHOc.361+11G= (n.361+11G=)
3g.129529105G>TCA546417607RHOc.361+11G>T (n.361+11G>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129529106G>ACA2704008221RHOc.361+12G>A (n.361+12G>A)
dbSNP
3g.129529107T>CCA546417608RHOc.361+13T>C (n.361+13T>C)
dbSNP gnomAD v2 gnomAD v4
3g.129529107T=CA1401206329RHOc.361+13T= (n.361+13T=)
3g.129529108G>ACA2607123RHOc.361+14G>A (n.361+14G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529108G=CA1401206335RHOc.361+14G= (n.361+14G=)

Number of alleles fetched