Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129528771T>ACA354495288RHOc.38T>A (p.Phe13Tyr)
3g.129528771T>CCA354495292RHOc.38T>C (p.Phe13Ser)
ClinVar
3g.129528771T>GCA354495290RHOc.38T>G (p.Phe13Cys)
3g.129528772C>ACA354495298RHOc.39C>A (p.Phe13Leu)
3g.129528772C>GCA354495300RHOc.39C>G (p.Phe13Leu)
3g.129528772C>TCA435768847RHOc.39C>T (p.Phe13=)
gnomAD v4
3g.129528773T>ACA354495301RHOc.40T>A (p.Ser14Thr)
3g.129528773T>CCA354495302RHOc.40T>C (p.Ser14Pro)
3g.129528773T>GCA354495303RHOc.40T>G (p.Ser14Ala)
3g.129528774C>ACA354495304RHOc.41C>A (p.Ser14Tyr)
3g.129528774C>GCA354495305RHOc.41C>G (p.Ser14Cys)
3g.129528774C>TCA354495307RHOc.41C>T (p.Ser14Phe)
gnomAD v4
3g.129528775C>ACA435768852RHOc.42C>A (p.Ser14=)
3g.129528775C=CA1401204982RHOc.42C= (p.Ser14=)
3g.129528775C>GCA435768854RHOc.42C>G (p.Ser14=)
3g.129528775C>TCA435768855RHOc.42C>T (p.Ser14=)
dbSNP gnomAD v3 gnomAD v4
3g.129528776A>CCA354495309RHOc.43A>C (p.Asn15His)
3g.129528776A>GCA354495323RHOc.43A>G (p.Asn15Asp)
ClinVar
3g.129528776A>TCA354495326RHOc.43A>T (p.Asn15Tyr)
3g.129528777A=CA1401204989RHOc.44A= (p.Asn15=)
3g.129528777A>CCA354495331RHOc.44A>C (p.Asn15Thr)
3g.129528777A>GCA256685RHOc.44A>G (p.Asn15Ser)
ClinVar dbSNP gnomAD v4
3g.129528777A>TCA354495329RHOc.44A>T (p.Asn15Ile)
ClinVar dbSNP
3g.129528778T>ACA354495336RHOc.45T>A (p.Asn15Lys)
ClinVar dbSNP
3g.129528778T>CCA435768858RHOc.45T>C (p.Asn15=)
3g.129528778T>GCA354495338RHOc.45T>G (p.Asn15Lys)
ClinVar dbSNP
3g.129528778T=CA1401205004RHOc.45T= (p.Asn15=)
3g.129528778_129528779delCA2704007051RHOc.45_46del (p.Ala16AspfsTer17)
dbSNP
3g.129528779G>ACA354495345RHOc.46G>A (p.Ala16Thr)
gnomAD v4
3g.129528779G>CCA354495346RHOc.46G>C (p.Ala16Pro)
3g.129528779G>TCA354495351RHOc.46G>T (p.Ala16Ser)
3g.129528780C>ACA354495354RHOc.47C>A (p.Ala16Glu)
gnomAD v4
3g.129528780C=CA1401205012RHOc.47C= (p.Ala16=)
3g.129528780C>GCA354495355RHOc.47C>G (p.Ala16Gly)
3g.129528780C>TCA2607043RHOc.47C>T (p.Ala16Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129528781G>ACA2607044RHOc.48G>A (p.Ala16=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528781G>CCA435768859RHOc.48G>C (p.Ala16=)
3g.129528781G=CA1401205020RHOc.48G= (p.Ala16=)
3g.129528781G>TCA435768860RHOc.48G>T (p.Ala16=)
dbSNP gnomAD v2 gnomAD v4
3g.129528781_129528782insTCCA2704007109RHOc.48_49insTC (p.Thr17SerfsTer?)
dbSNP
3g.129528782A=CA1401205030RHOc.49A= (p.Thr17=)
3g.129528782A>CCA354495365RHOc.49A>C (p.Thr17Pro)
3g.129528782A>GCA354495371RHOc.49A>G (p.Thr17Ala)
dbSNP gnomAD v2 gnomAD v4
3g.129528782A>TCA354495372RHOc.49A>T (p.Thr17Ser)
3g.129528783C>ACA354495380RHOc.50C>A (p.Thr17Lys)
ClinVar dbSNP
3g.129528783C=CA1401205042RHOc.50C= (p.Thr17=)
3g.129528783C>GCA354495381RHOc.50C>G (p.Thr17Arg)
3g.129528783C>TCA256665RHOc.50C>T (p.Thr17Met)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129528784G>ACA2607045RHOc.51G>A (p.Thr17=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
3g.129528784G>CCA2607046RHOc.51G>C (p.Thr17=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528784G=CA1401205049RHOc.51G= (p.Thr17=)
3g.129528784G>TCA435768861RHOc.51G>T (p.Thr17=)
dbSNP
3g.129528785G>ACA354495385RHOc.52G>A (p.Gly18Ser)
dbSNP gnomAD v4
3g.129528785G>CCA354495389RHOc.52G>C (p.Gly18Arg)
3g.129528785G>TCA354495391RHOc.52G>T (p.Gly18Cys)
gnomAD v4
3g.129528786G>ACA2607047RHOc.53G>A (p.Gly18Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528786G>CCA2607048RHOc.53G>C (p.Gly18Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129528786G=CA1401205059RHOc.53G= (p.Gly18=)
3g.129528786G>TCA354495405RHOc.53G>T (p.Gly18Val)
ClinVar dbSNP
3g.129528787T>ACA435768862RHOc.54T>A (p.Gly18=)
3g.129528787T>CCA435768863RHOc.54T>C (p.Gly18=)
dbSNP
3g.129528787T>GCA435768864RHOc.54T>G (p.Gly18=)
dbSNP gnomAD v4
3g.129528787T=CA1401205069RHOc.54T= (p.Gly18=)
3g.129528788G>ACA354495407RHOc.55G>A (p.Val19Met)
dbSNP gnomAD v2 gnomAD v4 COSMIC
3g.129528788G>CCA354495424RHOc.55G>C (p.Val19Leu)
3g.129528788G=CA1401205074RHOc.55G= (p.Val19=)
3g.129528788G>TCA354495416RHOc.55G>T (p.Val19Leu)
3g.129528789T>ACA354495426RHOc.56T>A (p.Val19Glu)
3g.129528789T>CCA354495430RHOc.56T>C (p.Val19Ala)
3g.129528789T>GCA354495432RHOc.56T>G (p.Val19Gly)
3g.129528790G>ACA2607049RHOc.57G>A (p.Val19=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129528790G>CCA435768865RHOc.57G>C (p.Val19=)
3g.129528790G=CA1401205082RHOc.57G= (p.Val19=)
3g.129528790G>TCA435768866RHOc.57G>T (p.Val19=)
3g.129528791G>ACA2607050RHOc.58G>A (p.Val20Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528791G>CCA354495445RHOc.58G>C (p.Val20Leu)
ClinVar
3g.129528791G=CA1401205090RHOc.58G= (p.Val20=)
3g.129528791G>TCA354495443RHOc.58G>T (p.Val20Leu)
3g.129528792T>ACA354495447RHOc.59T>A (p.Val20Glu)
3g.129528792T>CCA2607051RHOc.59T>C (p.Val20Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129528792T>GCA354495450RHOc.59T>G (p.Val20Gly)
3g.129528792T=CA1401205097RHOc.59T= (p.Val20=)
3g.129528793A=CA1401205103RHOc.60A= (p.Val20=)
3g.129528793A>CCA435768867RHOc.60A>C (p.Val20=)
3g.129528793A>GCA435768868RHOc.60A>G (p.Val20=)
dbSNP gnomAD v4
3g.129528793A>TCA435768869RHOc.60A>T (p.Val20=)
3g.129528794C>ACA354495451RHOc.61C>A (p.Arg21Ser)
3g.129528794C=CA1401205110RHOc.61C= (p.Arg21=)
3g.129528794C>GCA354495452RHOc.61C>G (p.Arg21Gly)
3g.129528794C>TCA354495454RHOc.61C>T (p.Arg21Cys)
dbSNP gnomAD v2 gnomAD v4 COSMIC
3g.129528795G>ACA2607052RHOc.62G>A (p.Arg21His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528795G>CCA354495457RHOc.62G>C (p.Arg21Pro)
ClinVar
3g.129528795G=CA1401205120RHOc.62G= (p.Arg21=)
3g.129528795G>TCA354495461RHOc.62G>T (p.Arg21Leu)
gnomAD v4
3g.129528796C>ACA435768870RHOc.63C>A (p.Arg21=)
3g.129528796C>GCA435768871RHOc.63C>G (p.Arg21=)
dbSNP
3g.129528796C>TCA435768872RHOc.63C>T (p.Arg21=)
gnomAD v4
3g.129528797A>CCA354495464RHOc.64A>C (p.Ser22Arg)
3g.129528797A>GCA354495465RHOc.64A>G (p.Ser22Gly)
3g.129528797A>TCA354495468RHOc.64A>T (p.Ser22Cys)
3g.129528798G>ACA2607053RHOc.65G>A (p.Ser22Asn)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528798G>CCA354495470RHOc.65G>C (p.Ser22Thr)
3g.129528798G=CA1401205131RHOc.65G= (p.Ser22=)
3g.129528798G>TCA354495472RHOc.65G>T (p.Ser22Ile)
3g.129528799C>ACA354495476RHOc.66C>A (p.Ser22Arg)
ClinVar dbSNP
3g.129528799C=CA1401205141RHOc.66C= (p.Ser22=)
3g.129528799C>GCA354495478RHOc.66C>G (p.Ser22Arg)
3g.129528799C>TCA2607054RHOc.66C>T (p.Ser22=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528800C>ACA354495488RHOc.67C>A (p.Pro23Thr)
ClinVar
3g.129528800C=CA1401205150RHOc.67C= (p.Pro23=)
3g.129528800C>GCA256695RHOc.67C>G (p.Pro23Ala)
ClinVar dbSNP
3g.129528800C>TCA354495494RHOc.67C>T (p.Pro23Ser)
ClinVar dbSNP
3g.129528801C>ACA256661RHOc.68C>A (p.Pro23His)
ClinVar dbSNP gnomAD v4
3g.129528801C=CA1401205168RHOc.68C= (p.Pro23=)
3g.129528801C>GCA354495499RHOc.68C>G (p.Pro23Arg)
3g.129528801C>TCA354495503RHOc.68C>T (p.Pro23Leu)
ClinVar dbSNP
3g.129528802C>ACA435768873RHOc.69C>A (p.Pro23=)
3g.129528802C>GCA435768874RHOc.69C>G (p.Pro23=)
3g.129528802C>TCA435768875RHOc.69C>T (p.Pro23=)
3g.129528803T>ACA354495507RHOc.70T>A (p.Phe24Ile)
3g.129528803T>CCA354495508RHOc.70T>C (p.Phe24Leu)
3g.129528803T>GCA354495510RHOc.70T>G (p.Phe24Val)
3g.129528804T>ACA354495518RHOc.71T>A (p.Phe24Tyr)
3g.129528804T>CCA354495517RHOc.71T>C (p.Phe24Ser)
ClinVar
3g.129528804T>GCA354495513RHOc.71T>G (p.Phe24Cys)
ClinVar
3g.129528805C>ACA354495523RHOc.72C>A (p.Phe24Leu)
ClinVar dbSNP
3g.129528805C=CA1401205181RHOc.72C= (p.Phe24=)
3g.129528805C>GCA2607055RHOc.72C>G (p.Phe24Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129528805C>TCA435768876RHOc.72C>T (p.Phe24=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129528806G>ACA2607056RHOc.73G>A (p.Glu25Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129528806G>CCA354495533RHOc.73G>C (p.Glu25Gln)
dbSNP
3g.129528806G=CA1401205190RHOc.73G= (p.Glu25=)
3g.129528806G>TCA354495534RHOc.73G>T (p.Glu25Ter)
3g.129528807A>CCA354495538RHOc.74A>C (p.Glu25Ala)
gnomAD v4
3g.129528807A>GCA354495539RHOc.74A>G (p.Glu25Gly)
3g.129528807A>TCA354495543RHOc.74A>T (p.Glu25Val)
3g.129528808G>ACA435768877RHOc.75G>A (p.Glu25=)
dbSNP gnomAD v2 gnomAD v4
3g.129528808G>CCA354495548RHOc.75G>C (p.Glu25Asp)
3g.129528808G=CA1401205196RHOc.75G= (p.Glu25=)
3g.129528808G>TCA2607057RHOc.75G>T (p.Glu25Asp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528809T>ACA354495553RHOc.76T>A (p.Tyr26Asn)
3g.129528809T>CCA354495556RHOc.76T>C (p.Tyr26His)
dbSNP
3g.129528809T>GCA354495557RHOc.76T>G (p.Tyr26Asp)
3g.129528810A=CA1401205201RHOc.77A= (p.Tyr26=)
3g.129528810A>CCA354495562RHOc.77A>C (p.Tyr26Ser)
3g.129528810A>GCA354495563RHOc.77A>G (p.Tyr26Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129528810A>TCA354495561RHOc.77A>T (p.Tyr26Phe)
3g.129528811C>ACA354495564RHOc.78C>A (p.Tyr26Ter)
dbSNP gnomAD v2
3g.129528811C=CA1401205208RHOc.78C= (p.Tyr26=)
3g.129528811C>GCA354495565RHOc.78C>G (p.Tyr26Ter)
dbSNP
3g.129528811C>TCA82646665RHOc.78C>T (p.Tyr26=)
dbSNP
3g.129528812C>ACA82646677RHOc.79C>A (p.Pro27Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129528812C=CA1401205215RHOc.79C= (p.Pro27=)
3g.129528812C>GCA354495566RHOc.79C>G (p.Pro27Ala)
3g.129528812C>TCA82646684RHOc.79C>T (p.Pro27Ser)
dbSNP gnomAD v3 gnomAD v4
3g.129528813C>ACA354495567RHOc.80C>A (p.Pro27Gln)
3g.129528813C>GCA354495568RHOc.80C>G (p.Pro27Arg)
3g.129528813C>TCA354495570RHOc.80C>T (p.Pro27Leu)
3g.129528814A>CCA435768878RHOc.81A>C (p.Pro27=)
3g.129528814A>GCA435768879RHOc.81A>G (p.Pro27=)
dbSNP
3g.129528814A>TCA435768880RHOc.81A>T (p.Pro27=)
3g.129528815C>ACA354495572RHOc.82C>A (p.Gln28Lys)
ClinVar dbSNP gnomAD v4
3g.129528815C>GCA354495577RHOc.82C>G (p.Gln28Glu)
ClinVar
3g.129528815C>TCA354495578RHOc.82C>T (p.Gln28Ter)
gnomAD v4
3g.129528816A=CA1401205223RHOc.83A= (p.Gln28=)
3g.129528816A>CCA354495581RHOc.83A>C (p.Gln28Pro)
3g.129528816A>GCA354495583RHOc.83A>G (p.Gln28Arg)
ClinVar dbSNP
3g.129528816A>TCA354495585RHOc.83A>T (p.Gln28Leu)
3g.129528817G>ACA435768881RHOc.84G>A (p.Gln28=)
3g.129528817G>CCA354495591RHOc.84G>C (p.Gln28His)
3g.129528817G>TCA354495588RHOc.84G>T (p.Gln28His)
ClinVar dbSNP
3g.129528818T>ACA354495592RHOc.85T>A (p.Tyr29Asn)
3g.129528818T>CCA354495595RHOc.85T>C (p.Tyr29His)
dbSNP gnomAD v2 gnomAD v4
3g.129528818T>GCA354495608RHOc.85T>G (p.Tyr29Asp)
3g.129528818T=CA1401205228RHOc.85T= (p.Tyr29=)
3g.129528819A=CA1401205230RHOc.86A= (p.Tyr29=)
3g.129528819A>CCA354495611RHOc.86A>C (p.Tyr29Ser)
3g.129528819A>GCA354495615RHOc.86A>G (p.Tyr29Cys)
ClinVar dbSNP
3g.129528819A>TCA354495617RHOc.86A>T (p.Tyr29Phe)
3g.129528820C>ACA354495618RHOc.87C>A (p.Tyr29Ter)
3g.129528820C=CA1401205239RHOc.87C= (p.Tyr29=)
3g.129528820C>GCA354495619RHOc.87C>G (p.Tyr29Ter)
3g.129528820C>TCA2607058RHOc.87C>T (p.Tyr29=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528821T>ACA354495620RHOc.88T>A (p.Tyr30Asn)
3g.129528821T>CCA354495621RHOc.88T>C (p.Tyr30His)
3g.129528821T>GCA354495622RHOc.88T>G (p.Tyr30Asp)
3g.129528822A>CCA354495632RHOc.89A>C (p.Tyr30Ser)
3g.129528822A>GCA354495629RHOc.89A>G (p.Tyr30Cys)
3g.129528822A>TCA354495626RHOc.89A>T (p.Tyr30Phe)
3g.129528823C>ACA354495636RHOc.90C>A (p.Tyr30Ter)
dbSNP gnomAD v3 gnomAD v4
3g.129528823C=CA1401205265RHOc.90C= (p.Tyr30=)
3g.129528823C>GCA354495639RHOc.90C>G (p.Tyr30Ter)
3g.129528823C>TCA435768882RHOc.90C>T (p.Tyr30=)
dbSNP gnomAD v2 gnomAD v4
3g.129528824C>ACA354495644RHOc.91C>A (p.Leu31Met)
3g.129528824C=CA1401205273RHOc.91C= (p.Leu31=)
3g.129528824C>GCA2607059RHOc.91C>G (p.Leu31Val)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129528824C>TCA435768883RHOc.91C>T (p.Leu31=)
dbSNP gnomAD v2 gnomAD v4
3g.129528825T>ACA354495647RHOc.92T>A (p.Leu31Gln)
3g.129528825T>CCA354495650RHOc.92T>C (p.Leu31Pro)
ClinVar
3g.129528825T>GCA354495654RHOc.92T>G (p.Leu31Arg)
3g.129528826G>ACA435768884RHOc.93G>A (p.Leu31=)
3g.129528826G>CCA435768885RHOc.93G>C (p.Leu31=)
3g.129528826G>TCA435768886RHOc.93G>T (p.Leu31=)
3g.129528827G>ACA354495667RHOc.94G>A (p.Ala32Thr)
3g.129528827G>CCA354495674RHOc.94G>C (p.Ala32Pro)
ClinVar dbSNP
3g.129528827G=CA1401205281RHOc.94G= (p.Ala32=)
3g.129528827G>TCA354495680RHOc.94G>T (p.Ala32Ser)
3g.129528828C>ACA354495685RHOc.95C>A (p.Ala32Asp)
3g.129528828C>GCA354495687RHOc.95C>G (p.Ala32Gly)
3g.129528828C>TCA354495691RHOc.95C>T (p.Ala32Val)
3g.129528829T>ACA435768887RHOc.96T>A (p.Ala32=)
3g.129528829T>CCA435768888RHOc.96T>C (p.Ala32=)
dbSNP gnomAD v4
3g.129528829T>GCA435768889RHOc.96T>G (p.Ala32=)
dbSNP
3g.129528829T=CA1401205289RHOc.96T= (p.Ala32=)
3g.129528830G>ACA354495693RHOc.97G>A (p.Glu33Lys)
gnomAD v4
3g.129528830G>CCA354495698RHOc.97G>C (p.Glu33Gln)
3g.129528830G>TCA354495695RHOc.97G>T (p.Glu33Ter)
3g.129528831A>CCA354495699RHOc.98A>C (p.Glu33Ala)
3g.129528831A>GCA354495701RHOc.98A>G (p.Glu33Gly)
3g.129528831A>TCA354495703RHOc.98A>T (p.Glu33Val)
3g.129528832G>ACA435768890RHOc.99G>A (p.Glu33=)
dbSNP gnomAD v4
3g.129528832G>CCA354495705RHOc.99G>C (p.Glu33Asp)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129528832G=CA1401205295RHOc.99G= (p.Glu33=)
3g.129528832G>TCA354495707RHOc.99G>T (p.Glu33Asp)
3g.129528833C>ACA354495709RHOc.100C>A (p.Pro34Thr)
3g.129528833C>GCA354495713RHOc.100C>G (p.Pro34Ala)
3g.129528833C>TCA354495715RHOc.100C>T (p.Pro34Ser)
gnomAD v4 COSMIC
3g.129528834C>ACA354495716RHOc.101C>A (p.Pro34Gln)
3g.129528834C>GCA354495717RHOc.101C>G (p.Pro34Arg)
3g.129528834C>TCA354495719RHOc.101C>T (p.Pro34Leu)
ClinVar dbSNP gnomAD v4
3g.129528835A=CA1401205299RHOc.102A= (p.Pro34=)
3g.129528835A>CCA435768891RHOc.102A>C (p.Pro34=)
3g.129528835A>GCA435768892RHOc.102A>G (p.Pro34=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129528835A>TCA435768893RHOc.102A>T (p.Pro34=)
3g.129528836T>ACA354495724RHOc.103T>A (p.Trp35Arg)
3g.129528836T>CCA354495726RHOc.103T>C (p.Trp35Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129528836T>GCA354495722RHOc.103T>G (p.Trp35Gly)
3g.129528836T=CA1401205310RHOc.103T= (p.Trp35=)
3g.129528837G>ACA354495730RHOc.104G>A (p.Trp35Ter)
3g.129528837G>CCA354495729RHOc.104G>C (p.Trp35Ser)
3g.129528837G>TCA354495741RHOc.104G>T (p.Trp35Leu)
3g.129528838G>ACA82646715RHOc.105G>A (p.Trp35Ter)
dbSNP
3g.129528838G>CCA354495746RHOc.105G>C (p.Trp35Cys)
3g.129528838G=CA1401205318RHOc.105G= (p.Trp35=)
3g.129528838G>TCA354495744RHOc.105G>T (p.Trp35Cys)
3g.129528839C>ACA2607060RHOc.106C>A (p.Gln36Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129528839C=CA1401205322RHOc.106C= (p.Gln36=)
3g.129528839C>GCA354495748RHOc.106C>G (p.Gln36Glu)
3g.129528839C>TCA354495749RHOc.106C>T (p.Gln36Ter)
ClinVar dbSNP
3g.129528840A=CA1401205334RHOc.107A= (p.Gln36=)
3g.129528840A>CCA354495752RHOc.107A>C (p.Gln36Pro)
3g.129528840A>GCA82646724RHOc.107A>G (p.Gln36Arg)
dbSNP gnomAD v4
3g.129528840A>TCA354495754RHOc.107A>T (p.Gln36Leu)
gnomAD v4 COSMIC
3g.129528841G>ACA82646725RHOc.108G>A (p.Gln36=)
dbSNP
3g.129528841G>CCA2607061RHOc.108G>C (p.Gln36His)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129528841G=CA1401205339RHOc.108G= (p.Gln36=)
3g.129528841G>TCA354495757RHOc.108G>T (p.Gln36His)
3g.129528842T>ACA354495758RHOc.109T>A (p.Phe37Ile)
3g.129528842T>CCA354495759RHOc.109T>C (p.Phe37Leu)
3g.129528842T>GCA354495761RHOc.109T>G (p.Phe37Val)
3g.129528843T>ACA354495768RHOc.110T>A (p.Phe37Tyr)
3g.129528843T>CCA354495766RHOc.110T>C (p.Phe37Ser)
3g.129528843T>GCA354495763RHOc.110T>G (p.Phe37Cys)
3g.129528844C>ACA354495769RHOc.111C>A (p.Phe37Leu)
3g.129528844C>GCA354495771RHOc.111C>G (p.Phe37Leu)
3g.129528844C>TCA435768894RHOc.111C>T (p.Phe37=)
3g.129528845T>ACA354495774RHOc.112T>A (p.Ser38Thr)
3g.129528845T>CCA354495777RHOc.112T>C (p.Ser38Pro)
gnomAD v4
3g.129528845T>GCA354495778RHOc.112T>G (p.Ser38Ala)
3g.129528846C>ACA354495779RHOc.113C>A (p.Ser38Tyr)
3g.129528846C>GCA354495780RHOc.113C>G (p.Ser38Cys)
gnomAD v4
3g.129528846C>TCA354495781RHOc.113C>T (p.Ser38Phe)
3g.129528847C>ACA435768895RHOc.114C>A (p.Ser38=)
dbSNP gnomAD v4
3g.129528847C=CA1401205347RHOc.114C= (p.Ser38=)
3g.129528847C>GCA435768896RHOc.114C>G (p.Ser38=)
3g.129528847C>TCA435768897RHOc.114C>T (p.Ser38=)
3g.129528848A=CA1401205357RHOc.115A= (p.Met39=)
3g.129528848A>CCA2607062RHOc.115A>C (p.Met39Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528848A>GCA354495783RHOc.115A>G (p.Met39Val)
ClinVar
3g.129528848A>TCA354495784RHOc.115A>T (p.Met39Leu)
3g.129528849T>ACA354495792RHOc.116T>A (p.Met39Lys)
3g.129528849T>CCA354495789RHOc.116T>C (p.Met39Thr)
3g.129528849T>GCA354495787RHOc.116T>G (p.Met39Arg)
ClinVar dbSNP gnomAD v4
3g.129528849T=CA1401205364RHOc.116T= (p.Met39=)
3g.129528850G>ACA354495795RHOc.117G>A (p.Met39Ile)
3g.129528850G>CCA354495796RHOc.117G>C (p.Met39Ile)
3g.129528850G>TCA354495797RHOc.117G>T (p.Met39Ile)
3g.129528851C>ACA354495801RHOc.118C>A (p.Leu40Met)
3g.129528851C=CA1401205370RHOc.118C= (p.Leu40=)
3g.129528851C>GCA354495803RHOc.118C>G (p.Leu40Val)
gnomAD v4
3g.129528851C>TCA2607063RHOc.118C>T (p.Leu40=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528852T>ACA354495809RHOc.119T>A (p.Leu40Gln)
3g.129528852T>CCA354495811RHOc.119T>C (p.Leu40Pro)
3g.129528852T>GCA354495813RHOc.119T>G (p.Leu40Arg)
3g.129528853G>ACA435768898RHOc.120G>A (p.Leu40=)
3g.129528853G>CCA435768899RHOc.120G>C (p.Leu40=)
3g.129528853G>TCA435768900RHOc.120G>T (p.Leu40=)
3g.129528854G>ACA82646751RHOc.121G>A (p.Ala41Thr)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.129528854G>CCA354495818RHOc.121G>C (p.Ala41Pro)
3g.129528854G=CA1401205371RHOc.121G= (p.Ala41=)
3g.129528854G>TCA354495819RHOc.121G>T (p.Ala41Ser)
3g.129528855C>ACA354495826RHOc.122C>A (p.Ala41Asp)
3g.129528855C>GCA354495823RHOc.122C>G (p.Ala41Gly)
3g.129528855C>TCA354495822RHOc.122C>T (p.Ala41Val)
3g.129528856C>ACA435768901RHOc.123C>A (p.Ala41=)
dbSNP
3g.129528856C=CA1401205376RHOc.123C= (p.Ala41=)
3g.129528856C>GCA435768902RHOc.123C>G (p.Ala41=)
3g.129528856C>TCA2607064RHOc.123C>T (p.Ala41=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129528856_129528857insAGGTAGTACTGTCA2528031382RHOc.123_124insAGGTAGTACTGT
3g.129528857G>ACA2607065RHOc.124G>A (p.Ala42Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129528857G>CCA354495831RHOc.124G>C (p.Ala42Pro)
3g.129528857G=CA1401205381RHOc.124G= (p.Ala42=)
3g.129528857G>TCA354495832RHOc.124G>T (p.Ala42Ser)
3g.129528857_129528860dupCA2667615084RHOc.124_127dup (p.Tyr43CysfsTer?)
gnomAD v4
3g.129528858C>ACA354495834RHOc.125C>A (p.Ala42Asp)
3g.129528858C>GCA354495836RHOc.125C>G (p.Ala42Gly)
3g.129528858C>TCA354495842RHOc.125C>T (p.Ala42Val)
gnomAD v4
3g.129528859C>ACA435768903RHOc.126C>A (p.Ala42=)
3g.129528859C>GCA435768904RHOc.126C>G (p.Ala42=)
dbSNP
3g.129528859C>TCA435768905RHOc.126C>T (p.Ala42=)
3g.129528860T>ACA354495843RHOc.127T>A (p.Tyr43Asn)
3g.129528860T>CCA354495845RHOc.127T>C (p.Tyr43His)
3g.129528860T>GCA354495847RHOc.127T>G (p.Tyr43Asp)
3g.129528861A=CA1401205384RHOc.128A= (p.Tyr43=)
3g.129528861A>CCA354495848RHOc.128A>C (p.Tyr43Ser)
3g.129528861A>GCA2607066RHOc.128A>G (p.Tyr43Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129528861A>TCA354495851RHOc.128A>T (p.Tyr43Phe)
3g.129528862C>ACA354495854RHOc.129C>A (p.Tyr43Ter)
3g.129528862C>GCA354495860RHOc.129C>G (p.Tyr43Ter)
3g.129528862C>TCA435768907RHOc.129C>T (p.Tyr43=)
gnomAD v4
3g.129528863A=CA1401205391RHOc.130A= (p.Met44=)
3g.129528863A>CCA354495864RHOc.130A>C (p.Met44Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.129528863A>GCA354495868RHOc.130A>G (p.Met44Val)
dbSNP gnomAD v3 gnomAD v4
3g.129528863A>TCA354495866RHOc.130A>T (p.Met44Leu)
3g.129528864T>ACA354495871RHOc.131T>A (p.Met44Lys)
3g.129528864T>CCA2607067RHOc.131T>C (p.Met44Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528864T>GCA354495873RHOc.131T>G (p.Met44Arg)
3g.129528864T=CA1401205396RHOc.131T= (p.Met44=)
3g.129528865G>ACA354495876RHOc.132G>A (p.Met44Ile)
gnomAD v4
3g.129528865G>CCA354495878RHOc.132G>C (p.Met44Ile)
3g.129528865G=CA1401205400RHOc.132G= (p.Met44=)
3g.129528865G>TCA354495880RHOc.132G>T (p.Met44Ile)
dbSNP gnomAD v3 gnomAD v4
3g.129528866T>ACA354495882RHOc.133T>A (p.Phe45Ile)
3g.129528866T>CCA256666RHOc.133T>C (p.Phe45Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528866T>GCA354495884RHOc.133T>G (p.Phe45Val)
3g.129528866T=CA1401205403RHOc.133T= (p.Phe45=)
3g.129528867T>ACA354495886RHOc.134T>A (p.Phe45Tyr)
3g.129528867T>CCA354495888RHOc.134T>C (p.Phe45Ser)
3g.129528867T>GCA354495889RHOc.134T>G (p.Phe45Cys)
3g.129528868T>ACA354495891RHOc.135T>A (p.Phe45Leu)
3g.129528868T>CCA435768908RHOc.135T>C (p.Phe45=)
dbSNP
3g.129528868T>GCA354495894RHOc.135T>G (p.Phe45Leu)
3g.129528869C>ACA354495899RHOc.136C>A (p.Leu46Met)
3g.129528869C>GCA354495902RHOc.136C>G (p.Leu46Val)
3g.129528869C>TCA435768909RHOc.136C>T (p.Leu46=)
3g.129528870T>ACA354495903RHOc.137T>A (p.Leu46Gln)
3g.129528870T>CCA354495904RHOc.137T>C (p.Leu46Pro)
3g.129528870T>GCA354495905RHOc.137T>G (p.Leu46Arg)
ClinVar dbSNP
3g.129528870T=CA1401205410RHOc.137T= (p.Leu46=)
3g.129528871G>ACA435768910RHOc.138G>A (p.Leu46=)
gnomAD v4
3g.129528871G>CCA435768911RHOc.138G>C (p.Leu46=)
3g.129528871G>TCA435768912RHOc.138G>T (p.Leu46=)

Number of alleles fetched