Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129533425_129533581delCA2758361862RHOc.937-183_937-27del (n.937-183_937-27del)
3g.129533558_129533572delinsAAGCACACTGTGGGCCA1401212978RHOc.937-50_937-36delinsAAGCACACTGTGGGC (n.937-50_937-36delinsAAGCACACTGTGGGC)
3g.129533559A>TCA2577961834RHOc.937-49A>T (n.937-49A>T)
3g.129533562_129533575delCA2607326RHOc.937-46_937-33del (n.937-46_937-33del)
dbSNP ExAC gnomAD v2
3g.129533560G>ACA2667618247RHOc.937-48G>A (n.937-48G>A)
gnomAD v4
3g.129533561C>ACA2667618249RHOc.937-47C>A (n.937-47C>A)
gnomAD v4
3g.129533561C>TCA2667618250RHOc.937-47C>T (n.937-47C>T)
gnomAD v4
3g.129533563C>ACA2667618254RHOc.937-45C>A (n.937-45C>A)
gnomAD v4
3g.129533563C=CA1401212984RHOc.937-45C= (n.937-45C=)
3g.129533563C>TCA2607328RHOc.937-45C>T (n.937-45C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129533564A>CCA2667618261RHOc.937-44A>C (n.937-44A>C)
gnomAD v4
3g.129533564A>GCA2667618270RHOc.937-44A>G (n.937-44A>G)
gnomAD v4
3g.129533565C>ACA2577961835RHOc.937-43C>A (n.937-43C>A)
gnomAD v4
3g.129533565C=CA1401212987RHOc.937-43C= (n.937-43C=)
3g.129533565C>TCA546212144RHOc.937-43C>T (n.937-43C>T)
dbSNP gnomAD v2
3g.129533566T>CCA1053436857RHOc.937-42T>C (n.937-42T>C)
dbSNP gnomAD v3 gnomAD v4
3g.129533566T=CA1401212989RHOc.937-42T= (n.937-42T=)
3g.129533567G>ACA2607329RHOc.937-41G>A (n.937-41G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129533567G=CA1401212992RHOc.937-41G= (n.937-41G=)
3g.129533568T>CCA2607330RHOc.937-40T>C (n.937-40T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129533568T=CA1401212994RHOc.937-40T= (n.937-40T=)
3g.129533571delCA2667618280RHOc.937-37del (n.937-37del)
gnomAD v4
3g.129533570G>ACA2607331RHOc.937-38G>A (n.937-38G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129533570G=CA1401212999RHOc.937-38G= (n.937-38G=)
3g.129533571G>ACA2667618285RHOc.937-37G>A (n.937-37G>A)
gnomAD v4
3g.129533572C>ACA2577961836RHOc.937-36C>A (n.937-36C>A)
gnomAD v4
3g.129533572C>TCA2667618287RHOc.937-36C>T (n.937-36C>T)
gnomAD v4
3g.129533574G>ACA2577961837RHOc.937-34G>A (n.937-34G>A)
gnomAD v4
3g.129533575C>ACA2667618290RHOc.937-33C>A (n.937-33C>A)
gnomAD v4
3g.129533575C=CA1401213002RHOc.937-33C= (n.937-33C=)
3g.129533575C>GCA546212154RHOc.937-33C>G (n.937-33C>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129533575C>TCA2577961838RHOc.937-33C>T (n.937-33C>T)
gnomAD v4
3g.129533576C>TCA2667618294RHOc.937-32C>T (n.937-32C>T)
gnomAD v4
3g.129533577C>ACA2667618331RHOc.937-31C>A (n.937-31C>A)
gnomAD v4
3g.129533577C=CA1401213005RHOc.937-31C= (n.937-31C=)
3g.129533577C>TCA82621188RHOc.937-31C>T (n.937-31C>T)
dbSNP gnomAD v4
3g.129533578T>ACA1401213012RHOc.937-30T>A (n.937-30T>A)
dbSNP gnomAD v4
3g.129533578T>CCA546212156RHOc.937-30T>C (n.937-30T>C)
dbSNP gnomAD v2 gnomAD v4
3g.129533578T>GCA546212158RHOc.937-30T>G (n.937-30T>G)
dbSNP gnomAD v2 gnomAD v4
3g.129533578T=CA1401213011RHOc.937-30T= (n.937-30T=)
3g.129533579G>CCA1401213016RHOc.937-29G>C (n.937-29G>C)
dbSNP
3g.129533579G=CA1401213015RHOc.937-29G= (n.937-29G=)
3g.129533579G>TCA2667618340RHOc.937-29G>T (n.937-29G>T)
gnomAD v4
3g.129533580delCA2667618338RHOc.937-28del (n.937-28del)
gnomAD v4
3g.129533580G>CCA2607332RHOc.937-28G>C (n.937-28G>C)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129533580G=CA1401213018RHOc.937-28G= (n.937-28G=)
3g.129533581C>ACA2667618346RHOc.937-27C>A (n.937-27C>A)
gnomAD v4
3g.129533581C=CA1401213021RHOc.937-27C= (n.937-27C=)
3g.129533581C>TCA82621198RHOc.937-27C>T (n.937-27C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129533581_129533589delCA2580068751RHOc.937-27_937-19del (n.937-27_937-19del)
ClinVar
3g.129533582C>ACA2607333RHOc.937-26C>A (n.937-26C>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129533582C=CA1401213023RHOc.937-26C= (n.937-26C=)
3g.129533582C>TCA2667618352RHOc.937-26C>T (n.937-26C>T)
gnomAD v4
3g.129533583C=CA1401213027RHOc.937-25C= (n.937-25C=)
3g.129533583C>GCA2607334RHOc.937-25C>G (n.937-25C>G)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129533584T>CCA2577961839RHOc.937-24T>C (n.937-24T>C)
gnomAD v4
3g.129533585G>ACA2607335RHOc.937-23G>A (n.937-23G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129533585G>CCA2739312820RHOc.937-23G>C (n.937-23G>C)
3g.129533585G=CA1401213029RHOc.937-23G= (n.937-23G=)
3g.129533585G>TCA1401213031RHOc.937-23G>T (n.937-23G>T)
dbSNP
3g.129533586A=CA1401213034RHOc.937-22A= (n.937-22A=)
3g.129533586A>TCA1401213036RHOc.937-22A>T (n.937-22A>T)
dbSNP
3g.129533587C>ACA2667618377RHOc.937-21C>A (n.937-21C>A)
gnomAD v4
3g.129533587C=CA1401213039RHOc.937-21C= (n.937-21C=)
3g.129533587C>TCA2607336RHOc.937-21C>T (n.937-21C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129533588T>CCA2577961840RHOc.937-20T>C (n.937-20T>C)
3g.129533589C>ACA2667618384RHOc.937-19C>A (n.937-19C>A)
gnomAD v4
3g.129533590A>GCA2667618389RHOc.937-18A>G (n.937-18A>G)
gnomAD v4
3g.129533593C>ACA2577961841RHOc.937-15C>A (n.937-15C>A)
gnomAD v4
3g.129533593C=CA1401213043RHOc.937-15C= (n.937-15C=)
3g.129533593C>GCA2607337RHOc.937-15C>G (n.937-15C>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129533594delCA2667618394RHOc.937-14del (n.937-14del)
gnomAD v4
3g.129533594C>ACA2667618409RHOc.937-14C>A (n.937-14C>A)
gnomAD v4
3g.129533594C=CA1401213046RHOc.937-14C= (n.937-14C=)
3g.129533594C>TCA2607338RHOc.937-14C>T (n.937-14C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129533595T>CCA2667618417RHOc.937-13T>C (n.937-13T>C)
gnomAD v4
3g.129533597T>CCA2667618423RHOc.937-11T>C (n.937-11T>C)
gnomAD v4
3g.129533598T>ACA1139655835RHOc.937-10T>A (n.937-10T>A)
ClinVar dbSNP
3g.129533598T>CCA2607339RHOc.937-10T>C (n.937-10T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129533598T=CA1401213051RHOc.937-10T= (n.937-10T=)
3g.129533599G>ACA82621233RHOc.937-9G>A (n.937-9G>A)
ClinVar dbSNP gnomAD v4
3g.129533599G>CCA82621242RHOc.937-9G>C (n.937-9G>C)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129533599G=CA1401213059RHOc.937-9G= (n.937-9G=)
3g.129533600C>ACA2577895299RHOc.937-8C>A (n.937-8C>A)
gnomAD v4
3g.129533600C>GCA2667618453RHOc.937-8C>G (n.937-8C>G)
gnomAD v4
3g.129533600C>TCA2667618448RHOc.937-8C>T (n.937-8C>T)
gnomAD v4
3g.129533601C>ACA2667618456RHOc.937-7C>A (n.937-7C>A)
gnomAD v4
3g.129533602T>ACA82621246RHOc.937-6T>A (n.937-6T>A)
ClinVar dbSNP gnomAD v4
3g.129533602T>CCA2607340RHOc.937-6T>C (n.937-6T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129533602T=CA1401213065RHOc.937-6T= (n.937-6T=)
3g.129533603T>CCA2667618525RHOc.937-5T>C (n.937-5T>C)
gnomAD v4
3g.129533604C=CA1401213070RHOc.937-4C= (n.937-4C=)
3g.129533604C>TCA546212180RHOc.937-4C>T (n.937-4C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129533605C=CA1401213073RHOc.937-3C= (n.937-3C=)
3g.129533605C>TCA1401213072RHOc.937-3C>T (n.937-3C>T)
dbSNP
3g.129533606A=CA1401213079RHOc.937-2A= (n.937-2A=)
3g.129533606A>CCA354471063RHOc.937-2A>C (n.937-2A>C)
ClinVar dbSNP
3g.129533606A>GCA354471064RHOc.937-2A>G (n.937-2A>G)
ClinVar dbSNP
3g.129533606A>TCA354471062RHOc.937-2A>T (n.937-2A>T)
ClinVar dbSNP
3g.129533606_129533615delCA2586965920RHOc.937-2_944del
3g.129533607G>ACA354471065RHOc.937-1G>A (n.937-1G>A)
ClinVar
3g.129533607G>CCA354471066RHOc.937-1G>C (n.937-1G>C)
ClinVar dbSNP
3g.129533607G=CA1401213084RHOc.937-1G= (n.937-1G=)
3g.129533607G>TCA354471067RHOc.937-1G>T (n.937-1G>T)
ClinVar gnomAD v4
3g.129533608T>ACA354471068RHOc.937T>A (p.Phe313Ile)
3g.129533608T>CCA354471069RHOc.937T>C (p.Phe313Leu)
3g.129533608T>GCA354471070RHOc.937T>G (p.Phe313Val)
3g.129533609T>ACA354471071RHOc.938T>A (p.Phe313Tyr)
3g.129533609T>CCA354471073RHOc.938T>C (p.Phe313Ser)
3g.129533609T>GCA354471072RHOc.938T>G (p.Phe313Cys)
3g.129533609_129533612delCA2577895300RHOc.938_941del (p.Phe313Ter)
3g.129533610C>ACA354471074RHOc.939C>A (p.Phe313Leu)
3g.129533610C>GCA354471075RHOc.939C>G (p.Phe313Leu)
3g.129533610C>TCA435623794RHOc.939C>T (p.Phe313=)
gnomAD v4
3g.129533611C>ACA435623795RHOc.940C>A (p.Arg314=)
3g.129533611C=CA1401213092RHOc.940C= (p.Arg314=)
3g.129533611C>GCA354471076RHOc.940C>G (p.Arg314Gly)
3g.129533611C>TCA2607341RHOc.940C>T (p.Arg314Trp)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129533612G>ACA2607342RHOc.941G>A (p.Arg314Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129533612G>CCA354471078RHOc.941G>C (p.Arg314Pro)
3g.129533612G=CA1401213101RHOc.941G= (p.Arg314=)
3g.129533612G>TCA354471077RHOc.941G>T (p.Arg314Leu)
dbSNP
3g.129533613dupCA2573332787RHOc.942dup (p.Asn315GlufsTer16)
3g.129533613delCA2580574309RHOc.942del (p.Asn315ThrfsTer?)
3g.129533613G>ACA435623796RHOc.942G>A (p.Arg314=)
3g.129533613G>CCA435623797RHOc.942G>C (p.Arg314=)
gnomAD v4
3g.129533613G>TCA435623798RHOc.942G>T (p.Arg314=)
3g.129533614A>CCA354471079RHOc.943A>C (p.Asn315His)
gnomAD v4
3g.129533614A>GCA354471081RHOc.943A>G (p.Asn315Asp)
3g.129533614A>TCA354471080RHOc.943A>T (p.Asn315Tyr)
3g.129533615A>CCA354471082RHOc.944A>C (p.Asn315Thr)
3g.129533615A>GCA354471083RHOc.944A>G (p.Asn315Ser)
3g.129533615A>TCA354471084RHOc.944A>T (p.Asn315Ile)
3g.129533616C>ACA354471085RHOc.945C>A (p.Asn315Lys)
gnomAD v4
3g.129533616C>GCA354471086RHOc.945C>G (p.Asn315Lys)
3g.129533616C>TCA435623799RHOc.945C>T (p.Asn315=)
dbSNP
3g.129533616_129533617delinsCTCA1401213107RHOc.945_946delinsCT (p.Asn315=)
3g.129533617delCA16617826RHOc.946del (p.Cys316AlafsTer?)
ClinVar dbSNP
3g.129533617T>ACA354471087RHOc.946T>A (p.Cys316Ser)
3g.129533617T>CCA354471088RHOc.946T>C (p.Cys316Arg)
3g.129533617T>GCA354471089RHOc.946T>G (p.Cys316Gly)
3g.129533618G>ACA354471090RHOc.947G>A (p.Cys316Tyr)
dbSNP gnomAD v2 gnomAD v4
3g.129533618G>CCA354471091RHOc.947G>C (p.Cys316Ser)
3g.129533618G=CA1401213122RHOc.947G= (p.Cys316=)
3g.129533618G>TCA354471092RHOc.947G>T (p.Cys316Phe)
COSMIC
3g.129533619C>ACA354471094RHOc.948C>A (p.Cys316Ter)
ClinVar
3g.129533619C=CA1401213128RHOc.948C= (p.Cys316=)
3g.129533619C>GCA354471093RHOc.948C>G (p.Cys316Trp)
dbSNP gnomAD v2 gnomAD v4
3g.129533619C>TCA2607343RHOc.948C>T (p.Cys316=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129533620A>CCA354471095RHOc.949A>C (p.Met317Leu)
3g.129533620A>GCA354471096RHOc.949A>G (p.Met317Val)
3g.129533620A>TCA354471097RHOc.949A>T (p.Met317Leu)
3g.129533621T>ACA2607344RHOc.950T>A (p.Met317Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129533621T>CCA354471098RHOc.950T>C (p.Met317Thr)
3g.129533621T>GCA354471099RHOc.950T>G (p.Met317Arg)
3g.129533621T=CA1401213134RHOc.950T= (p.Met317=)
3g.129533622G>ACA354471100RHOc.951G>A (p.Met317Ile)
3g.129533622G>CCA354471101RHOc.951G>C (p.Met317Ile)
3g.129533622G>TCA354471102RHOc.951G>T (p.Met317Ile)
3g.129533623C>ACA354471103RHOc.952C>A (p.Leu318Ile)
3g.129533623C=CA1401213140RHOc.952C= (p.Leu318=)
3g.129533623C>GCA2607345RHOc.952C>G (p.Leu318Val)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129533623C>TCA354471104RHOc.952C>T (p.Leu318Phe)
gnomAD v4
3g.129533623_129533626delinsCTCACA1401213142RHOc.952_955delinsCTCA (p.Leu318=)
3g.129533624T>ACA354471107RHOc.953T>A (p.Leu318His)
3g.129533624T>CCA354471106RHOc.953T>C (p.Leu318Pro)
3g.129533624T>GCA354471105RHOc.953T>G (p.Leu318Arg)
3g.129533624_129533626delCA1139655836RHOc.953_955del (p.Leu318_Thr319delinsPro)
ClinVar dbSNP gnomAD v4
3g.129533625C>ACA435623800RHOc.954C>A (p.Leu318=)
3g.129533625C=CA1401213149RHOc.954C= (p.Leu318=)
3g.129533625C>GCA435623801RHOc.954C>G (p.Leu318=)
3g.129533625C>TCA435623802RHOc.954C>T (p.Leu318=)
dbSNP gnomAD v4
3g.129533626A>CCA354471108RHOc.955A>C (p.Thr319Pro)
3g.129533626A>GCA354471109RHOc.955A>G (p.Thr319Ala)
3g.129533626A>TCA354471110RHOc.955A>T (p.Thr319Ser)
3g.129533627C>ACA354471111RHOc.956C>A (p.Thr319Asn)
dbSNP
3g.129533627C=CA1401213151RHOc.956C= (p.Thr319=)
3g.129533627C>GCA354471112RHOc.956C>G (p.Thr319Ser)
3g.129533627C>TCA354471113RHOc.956C>T (p.Thr319Ile)
dbSNP gnomAD v3 gnomAD v4
3g.129533628C>ACA435623803RHOc.957C>A (p.Thr319=)
3g.129533628C>GCA435623804RHOc.957C>G (p.Thr319=)
3g.129533628C>TCA435623805RHOc.957C>T (p.Thr319=)
3g.129533629A>CCA354471114RHOc.958A>C (p.Thr320Pro)
3g.129533629A>GCA354471115RHOc.958A>G (p.Thr320Ala)
gnomAD v4
3g.129533629A>TCA354471116RHOc.958A>T (p.Thr320Ser)
3g.129533630C>ACA2607346RHOc.959C>A (p.Thr320Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129533630C=CA1401213156RHOc.959C= (p.Thr320=)
3g.129533630C>GCA354471117RHOc.959C>G (p.Thr320Ser)
3g.129533630C>TCA354471118RHOc.959C>T (p.Thr320Ile)
dbSNP gnomAD v2 gnomAD v4
3g.129533631C>ACA435623806RHOc.960C>A (p.Thr320=)
3g.129533631C>GCA435623807RHOc.960C>G (p.Thr320=)
gnomAD v4
3g.129533631C>TCA435623808RHOc.960C>T (p.Thr320=)
COSMIC
3g.129533632A=CA1401213164RHOc.961A= (p.Ile321=)
3g.129533632A>CCA2607347RHOc.961A>C (p.Ile321Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129533632A>GCA354471120RHOc.961A>G (p.Ile321Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.129533632A>TCA354471119RHOc.961A>T (p.Ile321Phe)
3g.129533633T>ACA354471121RHOc.962T>A (p.Ile321Asn)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129533633T>CCA354471122RHOc.962T>C (p.Ile321Thr)
3g.129533633T>GCA354471123RHOc.962T>G (p.Ile321Ser)
3g.129533633T=CA1401213172RHOc.962T= (p.Ile321=)
3g.129533634C>ACA435623809RHOc.963C>A (p.Ile321=)
3g.129533634C>GCA354471124RHOc.963C>G (p.Ile321Met)
3g.129533634C>TCA435623810RHOc.963C>T (p.Ile321=)
3g.129533635T>ACA354471125RHOc.964T>A (p.Cys322Ser)
3g.129533635T>CCA354471126RHOc.964T>C (p.Cys322Arg)
3g.129533635T>GCA354471127RHOc.964T>G (p.Cys322Gly)
3g.129533636G>ACA354471128RHOc.965G>A (p.Cys322Tyr)
dbSNP gnomAD v2 gnomAD v4
3g.129533636G>CCA354471129RHOc.965G>C (p.Cys322Ser)
3g.129533636G=CA1401213178RHOc.965G= (p.Cys322=)
3g.129533636G>TCA354471130RHOc.965G>T (p.Cys322Phe)
gnomAD v4
3g.129533636_129533637delinsAACA2586965921RHOc.965_966delinsAA (p.Cys322Ter)
3g.129533637C>ACA354471131RHOc.966C>A (p.Cys322Ter)
3g.129533637C>GCA354471132RHOc.966C>G (p.Cys322Trp)
3g.129533637C>TCA435623811RHOc.966C>T (p.Cys322=)
gnomAD v4
3g.129533638T>ACA354471133RHOc.967T>A (p.Cys323Ser)
3g.129533638T>CCA354471135RHOc.967T>C (p.Cys323Arg)
3g.129533638T>GCA354471134RHOc.967T>G (p.Cys323Gly)
3g.129533639G>ACA354471136RHOc.968G>A (p.Cys323Tyr)
dbSNP gnomAD v2 gnomAD v4
3g.129533639G>CCA354471138RHOc.968G>C (p.Cys323Ser)
3g.129533639G=CA1401213182RHOc.968G= (p.Cys323=)
3g.129533639G>TCA354471137RHOc.968G>T (p.Cys323Phe)
3g.129533640C>ACA354471139RHOc.969C>A (p.Cys323Ter)
ClinVar dbSNP
3g.129533640C=CA1401213189RHOc.969C= (p.Cys323=)
3g.129533640C>GCA354471140RHOc.969C>G (p.Cys323Trp)
3g.129533640C>TCA2607348RHOc.969C>T (p.Cys323=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129533641G>ACA2607349RHOc.970G>A (p.Gly324Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129533641G>CCA354471141RHOc.970G>C (p.Gly324Arg)
3g.129533641G=CA1401213196RHOc.970G= (p.Gly324=)
3g.129533641G>TCA354471142RHOc.970G>T (p.Gly324Cys)
3g.129533642G>ACA354471143RHOc.971G>A (p.Gly324Asp)
gnomAD v4
3g.129533642G>CCA2607350RHOc.971G>C (p.Gly324Ala)
dbSNP ExAC gnomAD v4
3g.129533642G=CA1401213204RHOc.971G= (p.Gly324=)
3g.129533642G>TCA354471144RHOc.971G>T (p.Gly324Val)
3g.129533643C>ACA435623812RHOc.972C>A (p.Gly324=)
3g.129533643C>GCA435623813RHOc.972C>G (p.Gly324=)
3g.129533643C>TCA435623814RHOc.972C>T (p.Gly324=)
gnomAD v4
3g.129533644A>CCA354471145RHOc.973A>C (p.Lys325Gln)
3g.129533644A>GCA354471146RHOc.973A>G (p.Lys325Glu)
3g.129533644A>TCA354471147RHOc.973A>T (p.Lys325Ter)
3g.129533645A>CCA354471148RHOc.974A>C (p.Lys325Thr)
ClinVar dbSNP
3g.129533645A>GCA354471149RHOc.974A>G (p.Lys325Arg)
3g.129533645A>TCA354471150RHOc.974A>T (p.Lys325Met)
3g.129533646G>ACA435623815RHOc.975G>A (p.Lys325=)
gnomAD v4
3g.129533646G>CCA354471151RHOc.975G>C (p.Lys325Asn)
3g.129533646G>TCA354471152RHOc.975G>T (p.Lys325Asn)
COSMIC
3g.129533646_129533647delinsGACA1401213206RHOc.975_976delinsGA (p.Lys325=)
3g.129533647A>CCA354471153RHOc.976A>C (p.Asn326His)
3g.129533647A>GCA354471154RHOc.976A>G (p.Asn326Asp)
3g.129533647A>TCA354471155RHOc.976A>T (p.Asn326Tyr)
3g.129533647_129533648delCA2573320762RHOc.976_977del (p.Asn326ProfsTer4)
3g.129533648delCA1139655837RHOc.977del (p.Asn326ThrfsTer?)
ClinVar dbSNP
3g.129533647_129533651delinsAACCCCA1401213215RHOc.976_980delinsAACCC (p.Asn326=)
3g.129533648A=CA1401213222RHOc.977A= (p.Asn326=)
3g.129533648A>CCA354471156RHOc.977A>C (p.Asn326Thr)
3g.129533648A>GCA354471157RHOc.977A>G (p.Asn326Ser)
ClinVar dbSNP gnomAD v4
3g.129533648A>TCA354471158RHOc.977A>T (p.Asn326Ile)
3g.129533648_129533650delinsACCCA1401213224RHOc.977_979delinsACC (p.Asn326=)
3g.129533650_129533653delCA270026RHOc.979_982del (p.Pro327TrpfsTer?)
ClinVar dbSNP
3g.129533649C>ACA354471159RHOc.978C>A (p.Asn326Lys)
3g.129533649C=CA1401213236RHOc.978C= (p.Asn326=)
3g.129533649C>GCA354471160RHOc.978C>G (p.Asn326Lys)
3g.129533649C>TCA435623816RHOc.978C>T (p.Asn326=)
dbSNP
3g.129533651delCA2579758050RHOc.980del (p.Pro327HisfsTer?)
3g.129533650_129533651delCA915941575RHOc.979_980del (p.Pro327ThrfsTer3)
ClinVar dbSNP
3g.129533650C>ACA354471161RHOc.979C>A (p.Pro327Thr)
dbSNP gnomAD v4
3g.129533650C=CA1401213243RHOc.979C= (p.Pro327=)
3g.129533650C>GCA2607351RHOc.979C>G (p.Pro327Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129533650C>TCA354471162RHOc.979C>T (p.Pro327Ser)
3g.129533651C>ACA354471163RHOc.980C>A (p.Pro327Gln)
3g.129533651C=CA1401213246RHOc.980C= (p.Pro327=)
3g.129533651C>GCA354471165RHOc.980C>G (p.Pro327Arg)
dbSNP
3g.129533651C>TCA354471164RHOc.980C>T (p.Pro327Leu)
3g.129533652A=CA1401213248RHOc.981A= (p.Pro327=)
3g.129533652A>CCA435623817RHOc.981A>C (p.Pro327=)
dbSNP gnomAD v4
3g.129533652A>GCA435623818RHOc.981A>G (p.Pro327=)
3g.129533652A>TCA435623819RHOc.981A>T (p.Pro327=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129533653delCA2579758043RHOc.982del (p.Leu328TrpfsTer?)
3g.129533653C>ACA354471166RHOc.982C>A (p.Leu328Met)
3g.129533653C>GCA354471167RHOc.982C>G (p.Leu328Val)
gnomAD v4
3g.129533653C>TCA435623820RHOc.982C>T (p.Leu328=)
3g.129533654T>ACA354471168RHOc.983T>A (p.Leu328Gln)
3g.129533654T>CCA2607352RHOc.983T>C (p.Leu328Pro)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129533654T>GCA354471169RHOc.983T>G (p.Leu328Arg)
gnomAD v4
3g.129533654T=CA1401213253RHOc.983T= (p.Leu328=)
3g.129533655G>ACA435623821RHOc.984G>A (p.Leu328=)
COSMIC
3g.129533655G>CCA435623822RHOc.984G>C (p.Leu328=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129533655G=CA1401213256RHOc.984G= (p.Leu328=)
3g.129533655G>TCA435623823RHOc.984G>T (p.Leu328=)
3g.129533656G>ACA354471170RHOc.985G>A (p.Gly329Ser)
3g.129533656G>CCA354471171RHOc.985G>C (p.Gly329Arg)
gnomAD v4
3g.129533656G>TCA354471172RHOc.985G>T (p.Gly329Cys)
3g.129533657G>ACA354471173RHOc.986G>A (p.Gly329Asp)
ClinVar gnomAD v4
3g.129533657G>CCA354471174RHOc.986G>C (p.Gly329Ala)
3g.129533657G>TCA354471175RHOc.986G>T (p.Gly329Val)
3g.129533658T>ACA435623824RHOc.987T>A (p.Gly329=)
3g.129533658T>CCA435623825RHOc.987T>C (p.Gly329=)
3g.129533658T>GCA435623826RHOc.987T>G (p.Gly329=)
3g.129533659G>ACA354471178RHOc.988G>A (p.Asp330Asn)
3g.129533659G>CCA354471177RHOc.988G>C (p.Asp330His)
3g.129533659G>TCA354471176RHOc.988G>T (p.Asp330Tyr)

Number of alleles fetched