Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129532268_129532358dupCA915941573RHOc.548_638dup (p.Ile214AlafsTer?)
ClinVar 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)
3g.129532312G>ACA354469750RHOc.592G>A (p.Val198Ile)
gnomAD v4
3g.129532312G>CCA354469751RHOc.592G>C (p.Val198Leu)
3g.129532312G>TCA354469753RHOc.592G>T (p.Val198Phe)
3g.129532313T>ACA354469755RHOc.593T>A (p.Val198Asp)
3g.129532313T>CCA2607215RHOc.593T>C (p.Val198Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532313T>GCA354469756RHOc.593T>G (p.Val198Gly)
3g.129532313T=CA1401211122RHOc.593T= (p.Val198=)
3g.129532313_129532316delinsTCAACA1401211121RHOc.593_596delinsTCAA (p.Val198=)
3g.129532314C>ACA435768942RHOc.594C>A (p.Val198=)
3g.129532314C=CA1401211128RHOc.594C= (p.Val198=)
3g.129532314C>GCA2607217RHOc.594C>G (p.Val198=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532314C>TCA435768944RHOc.594C>T (p.Val198=)
3g.129532318_129532320delCA2607216RHOc.598_600del (p.Asn200del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532315A>CCA354469759RHOc.595A>C (p.Asn199His)
3g.129532315A>GCA354469761RHOc.595A>G (p.Asn199Asp)
gnomAD v4
3g.129532315A>TCA354469762RHOc.595A>T (p.Asn199Tyr)
3g.129532316delCA2667616874RHOc.596del (p.Asn199ThrfsTer18)
gnomAD v4
3g.129532316A>CCA354469763RHOc.596A>C (p.Asn199Thr)
3g.129532316A>GCA354469765RHOc.596A>G (p.Asn199Ser)
gnomAD v4
3g.129532316A>TCA354469767RHOc.596A>T (p.Asn199Ile)
3g.129532317C>ACA354469769RHOc.597C>A (p.Asn199Lys)
gnomAD v4
3g.129532317C=CA1401211132RHOc.597C= (p.Asn199=)
3g.129532317C>GCA2607218RHOc.597C>G (p.Asn199Lys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532317C>TCA435768947RHOc.597C>T (p.Asn199=)
gnomAD v4
3g.129532318A=CA1401211136RHOc.598A= (p.Asn200=)
3g.129532318A>CCA354469771RHOc.598A>C (p.Asn200His)
3g.129532318A>GCA82620494RHOc.598A>G (p.Asn200Asp)
dbSNP gnomAD v4
3g.129532318A>TCA354469772RHOc.598A>T (p.Asn200Tyr)
3g.129532319A>CCA354469774RHOc.599A>C (p.Asn200Thr)
3g.129532319A>GCA354469777RHOc.599A>G (p.Asn200Ser)
3g.129532319A>TCA354469775RHOc.599A>T (p.Asn200Ile)
3g.129532320C>ACA354469780RHOc.600C>A (p.Asn200Lys)
gnomAD v4
3g.129532320C=CA1401211144RHOc.600C= (p.Asn200=)
3g.129532320C>GCA354469781RHOc.600C>G (p.Asn200Lys)
3g.129532320C>TCA2607219RHOc.600C>T (p.Asn200=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532321G>ACA354469783RHOc.601G>A (p.Glu201Lys)
dbSNP gnomAD v4
3g.129532321G>CCA354469785RHOc.601G>C (p.Glu201Gln)
3g.129532321G=CA1401211155RHOc.601G= (p.Glu201=)
3g.129532321G>TCA2607220RHOc.601G>T (p.Glu201Ter)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
3g.129532322A=CA1401211157RHOc.602A= (p.Glu201=)
3g.129532322A>CCA354469788RHOc.602A>C (p.Glu201Ala)
3g.129532322A>GCA354469790RHOc.602A>G (p.Glu201Gly)
gnomAD v4
3g.129532322A>TCA354469791RHOc.602A>T (p.Glu201Val)
dbSNP
3g.129532323G>ACA435768951RHOc.603G>A (p.Glu201=)
dbSNP gnomAD v4
3g.129532323G>CCA354469793RHOc.603G>C (p.Glu201Asp)
3g.129532323G>TCA354469795RHOc.603G>T (p.Glu201Asp)
3g.129532324T>ACA354469799RHOc.604T>A (p.Ser202Thr)
3g.129532324T>CCA354469798RHOc.604T>C (p.Ser202Pro)
3g.129532324T>GCA354469797RHOc.604T>G (p.Ser202Ala)
3g.129532325C>ACA354469801RHOc.605C>A (p.Ser202Tyr)
3g.129532325C>GCA354469803RHOc.605C>G (p.Ser202Cys)
3g.129532325C>TCA354469805RHOc.605C>T (p.Ser202Phe)
3g.129532326T>ACA435768954RHOc.606T>A (p.Ser202=)
3g.129532326T>CCA82620501RHOc.606T>C (p.Ser202=)
dbSNP gnomAD v2
3g.129532326T>GCA435768955RHOc.606T>G (p.Ser202=)
dbSNP
3g.129532326T=CA1401211160RHOc.606T= (p.Ser202=)
3g.129532327T>ACA354469807RHOc.607T>A (p.Phe203Ile)
3g.129532327T>CCA354469808RHOc.607T>C (p.Phe203Leu)
3g.129532327T>GCA354469810RHOc.607T>G (p.Phe203Val)
3g.129532328T>ACA354469811RHOc.608T>A (p.Phe203Tyr)
3g.129532328T>CCA354469813RHOc.608T>C (p.Phe203Ser)
ClinVar dbSNP
3g.129532328T>GCA354469814RHOc.608T>G (p.Phe203Cys)
3g.129532329T>ACA354469815RHOc.609T>A (p.Phe203Leu)
3g.129532329T>CCA435768960RHOc.609T>C (p.Phe203=)
dbSNP gnomAD v4
3g.129532329T>GCA354469816RHOc.609T>G (p.Phe203Leu)
3g.129532330G>ACA354469821RHOc.610G>A (p.Val204Ile)
3g.129532330G>CCA354469819RHOc.610G>C (p.Val204Leu)
gnomAD v4
3g.129532330G>TCA354469817RHOc.610G>T (p.Val204Phe)
3g.129532331T>ACA354469823RHOc.611T>A (p.Val204Asp)
3g.129532331T>CCA354469824RHOc.611T>C (p.Val204Ala)
3g.129532331T>GCA354469826RHOc.611T>G (p.Val204Gly)
3g.129532332C>ACA435768963RHOc.612C>A (p.Val204=)
3g.129532332C>GCA435768964RHOc.612C>G (p.Val204=)
3g.129532332C>TCA435768967RHOc.612C>T (p.Val204=)
3g.129532333A=CA1401211164RHOc.613A= (p.Ile205=)
3g.129532333A>CCA354469827RHOc.613A>C (p.Ile205Leu)
3g.129532333A>GCA82620505RHOc.613A>G (p.Ile205Val)
ClinVar dbSNP gnomAD v4
3g.129532333A>TCA354469829RHOc.613A>T (p.Ile205Phe)
gnomAD v4
3g.129532334T>ACA354469830RHOc.614T>A (p.Ile205Asn)
3g.129532334T>CCA354469831RHOc.614T>C (p.Ile205Thr)
gnomAD v4
3g.129532334T>GCA10615279RHOc.614T>G (p.Ile205Ser)
ClinVar dbSNP
3g.129532334T=CA1401211170RHOc.614T= (p.Ile205=)
3g.129532336_129532344delCA2579758046RHOc.616_624del (p.Tyr206_Phe208del)
3g.129532335C>ACA435768970RHOc.615C>A (p.Ile205=)
3g.129532335C>GCA354469834RHOc.615C>G (p.Ile205Met)
gnomAD v4
3g.129532335C>TCA435768971RHOc.615C>T (p.Ile205=)
3g.129532336T>ACA354469835RHOc.616T>A (p.Tyr206Asn)
3g.129532336T>CCA354469837RHOc.616T>C (p.Tyr206His)
COSMIC
3g.129532336T>GCA354469839RHOc.616T>G (p.Tyr206Asp)
3g.129532337A>CCA354469840RHOc.617A>C (p.Tyr206Ser)
ClinVar
3g.129532337A>GCA354469843RHOc.617A>G (p.Tyr206Cys)
3g.129532337A>TCA354469841RHOc.617A>T (p.Tyr206Phe)
3g.129532338C>ACA354469845RHOc.618C>A (p.Tyr206Ter)
3g.129532338C=CA1401211179RHOc.618C= (p.Tyr206=)
3g.129532338C>GCA354469846RHOc.618C>G (p.Tyr206Ter)
3g.129532338C>TCA435768974RHOc.618C>T (p.Tyr206=)
dbSNP
3g.129532339A=CA1401211181RHOc.619A= (p.Met207=)
3g.129532339A>CCA354469848RHOc.619A>C (p.Met207Leu)
3g.129532339A>GCA2607221RHOc.619A>G (p.Met207Val)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532339A>TCA354469850RHOc.619A>T (p.Met207Leu)
3g.129532340T>ACA354469852RHOc.620T>A (p.Met207Lys)
3g.129532340T>CCA354469853RHOc.620T>C (p.Met207Thr)
dbSNP gnomAD v4 COSMIC
3g.129532340T>GCA256686RHOc.620T>G (p.Met207Arg)
ClinVar dbSNP
3g.129532340T=CA1401211196RHOc.620T= (p.Met207=)
3g.129532341G>ACA354469856RHOc.621G>A (p.Met207Ile)
gnomAD v4
3g.129532341G>CCA354469857RHOc.621G>C (p.Met207Ile)
3g.129532341G>TCA354469858RHOc.621G>T (p.Met207Ile)
gnomAD v4
3g.129532342T>ACA354469861RHOc.622T>A (p.Phe208Ile)
COSMIC
3g.129532342T>CCA354469863RHOc.622T>C (p.Phe208Leu)
3g.129532342T>GCA354469860RHOc.622T>G (p.Phe208Val)
3g.129532343T>ACA354469868RHOc.623T>A (p.Phe208Tyr)
3g.129532343T>CCA354469865RHOc.623T>C (p.Phe208Ser)
3g.129532343T>GCA354469867RHOc.623T>G (p.Phe208Cys)
dbSNP
3g.129532344C>ACA354469870RHOc.624C>A (p.Phe208Leu)
gnomAD v4
3g.129532344C=CA1401211202RHOc.624C= (p.Phe208=)
3g.129532344C>GCA2607223RHOc.624C>G (p.Phe208Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532344C>TCA2607222RHOc.624C>T (p.Phe208=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532345G>ACA2607224RHOc.625G>A (p.Val209Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532345G>CCA354469872RHOc.625G>C (p.Val209Leu)
3g.129532345G=CA1401211210RHOc.625G= (p.Val209=)
3g.129532345G>TCA354469873RHOc.625G>T (p.Val209Leu)
3g.129532346T>ACA354469875RHOc.626T>A (p.Val209Glu)
3g.129532346T>CCA354469877RHOc.626T>C (p.Val209Ala)
3g.129532346T>GCA354469878RHOc.626T>G (p.Val209Gly)
3g.129532347G>ACA435768984RHOc.627G>A (p.Val209=)
3g.129532347G>CCA435768985RHOc.627G>C (p.Val209=)
3g.129532347G=CA1401211213RHOc.627G= (p.Val209=)
3g.129532347G>TCA435768986RHOc.627G>T (p.Val209=)
dbSNP gnomAD v2
3g.129532348G>ACA2607226RHOc.628G>A (p.Val210Ile)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532348G>CCA354469881RHOc.628G>C (p.Val210Leu)
3g.129532348G=CA1401211218RHOc.628G= (p.Val210=)
3g.129532348G>TCA2607225RHOc.628G>T (p.Val210Phe)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532349T>ACA354469883RHOc.629T>A (p.Val210Asp)
3g.129532349T>CCA354469884RHOc.629T>C (p.Val210Ala)
3g.129532349T>GCA354469886RHOc.629T>G (p.Val210Gly)
3g.129532350C>ACA435768992RHOc.630C>A (p.Val210=)
3g.129532350C=CA1401211223RHOc.630C= (p.Val210=)
3g.129532350C>GCA435768994RHOc.630C>G (p.Val210=)
gnomAD v4
3g.129532350C>TCA2607227RHOc.630C>T (p.Val210=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532351C>ACA354469888RHOc.631C>A (p.His211Asn)
3g.129532351C=CA1401211228RHOc.631C= (p.His211=)
3g.129532351C>GCA354469890RHOc.631C>G (p.His211Asp)
3g.129532351C>TCA354469892RHOc.631C>T (p.His211Tyr)
ClinVar dbSNP
3g.129532352A=CA1401211236RHOc.632A= (p.His211=)
3g.129532352A>CCA256674RHOc.632A>C (p.His211Pro)
ClinVar dbSNP
3g.129532352A>GCA354469894RHOc.632A>G (p.His211Arg)
ClinVar dbSNP
3g.129532352A>TCA354469895RHOc.632A>T (p.His211Leu)
3g.129532353C>ACA354469897RHOc.633C>A (p.His211Gln)
3g.129532353C=CA1401211242RHOc.633C= (p.His211=)
3g.129532353C>GCA354469899RHOc.633C>G (p.His211Gln)
3g.129532353C>TCA2607228RHOc.633C>T (p.His211=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532354T>ACA354469902RHOc.634T>A (p.Phe212Ile)
3g.129532354T>CCA354469904RHOc.634T>C (p.Phe212Leu)
3g.129532354T>GCA354469901RHOc.634T>G (p.Phe212Val)
3g.129532355T>ACA354469906RHOc.635T>A (p.Phe212Tyr)
3g.129532355T>CCA354469907RHOc.635T>C (p.Phe212Ser)
3g.129532355T>GCA354469909RHOc.635T>G (p.Phe212Cys)
3g.129532356C>ACA354469911RHOc.636C>A (p.Phe212Leu)
3g.129532356C>GCA354469913RHOc.636C>G (p.Phe212Leu)
3g.129532356C>TCA435768998RHOc.636C>T (p.Phe212=)
3g.129532357A>CCA354469914RHOc.637A>C (p.Thr213Pro)
3g.129532357A>GCA354469916RHOc.637A>G (p.Thr213Ala)
3g.129532357A>TCA354469918RHOc.637A>T (p.Thr213Ser)
3g.129532358C>ACA354469920RHOc.638C>A (p.Thr213Asn)
dbSNP
3g.129532358C=CA1401211246RHOc.638C= (p.Thr213=)
3g.129532358C>GCA354469921RHOc.638C>G (p.Thr213Ser)
3g.129532358C>TCA354469923RHOc.638C>T (p.Thr213Ile)
dbSNP
3g.129532359C>ACA435769003RHOc.639C>A (p.Thr213=)
3g.129532359C=CA1401211249RHOc.639C= (p.Thr213=)
3g.129532359C>GCA82620540RHOc.639C>G (p.Thr213=)
dbSNP
3g.129532359C>TCA435769004RHOc.639C>T (p.Thr213=)
COSMIC
3g.129532360A=CA1401211251RHOc.640A= (p.Ile214=)
3g.129532360A>CCA354469925RHOc.640A>C (p.Ile214Leu)
3g.129532360A>GCA82620545RHOc.640A>G (p.Ile214Val)
dbSNP
3g.129532360A>TCA354469926RHOc.640A>T (p.Ile214Phe)
3g.129532361T>ACA354469932RHOc.641T>A (p.Ile214Asn)
ClinVar
3g.129532361T>CCA354469931RHOc.641T>C (p.Ile214Thr)
gnomAD v4
3g.129532361T>GCA354469929RHOc.641T>G (p.Ile214Ser)
3g.129532361_129532362insTCCTCACCAACTCTCTGCGTGGCATAGCCCTAGCA2758361646RHOc.641_642insTCCTCACCAACTCTCTGCGTGGCATAGCCCTAG (p.Ile214_Pro215insProHisGlnLeuSerAlaTrpHisSerProSer)
3g.129532362C>ACA2607229RHOc.642C>A (p.Ile214=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532362C=CA1401211253RHOc.642C= (p.Ile214=)
3g.129532362C>GCA354469934RHOc.642C>G (p.Ile214Met)
3g.129532362C>TCA2607230RHOc.642C>T (p.Ile214=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532363C>ACA354469937RHOc.643C>A (p.Pro215Thr)
3g.129532363C>GCA354469938RHOc.643C>G (p.Pro215Ala)
ClinVar dbSNP
3g.129532363C>TCA354469939RHOc.643C>T (p.Pro215Ser)
3g.129532364C>ACA354469942RHOc.644C>A (p.Pro215His)
3g.129532364C=CA1401211255RHOc.644C= (p.Pro215=)
3g.129532364C>GCA354469943RHOc.644C>G (p.Pro215Arg)
3g.129532364C>TCA354469945RHOc.644C>T (p.Pro215Leu)
ClinVar dbSNP
3g.129532365C>ACA435769005RHOc.645C>A (p.Pro215=)
gnomAD v4
3g.129532365C>GCA435769006RHOc.645C>G (p.Pro215=)
gnomAD v4
3g.129532365C>TCA435769007RHOc.645C>T (p.Pro215=)
dbSNP
3g.129532365_129532366delinsCACA1401211258RHOc.645_646delinsCA (p.Pro215=)
3g.129532366delCA2607231RHOc.646del (p.Met216Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532366A=CA1401211262RHOc.646A= (p.Met216=)
3g.129532366A>CCA354469947RHOc.646A>C (p.Met216Leu)
3g.129532366A>GCA354469949RHOc.646A>G (p.Met216Val)
3g.129532366A>TCA354469950RHOc.646A>T (p.Met216Leu)
dbSNP gnomAD v2 gnomAD v4
3g.129532367T>ACA354469952RHOc.647T>A (p.Met216Lys)
ClinVar dbSNP
3g.129532367T>CCA354469955RHOc.647T>C (p.Met216Thr)
3g.129532367T>GCA82620557RHOc.647T>G (p.Met216Arg)
ClinVar dbSNP
3g.129532367T=CA1401211267RHOc.647T= (p.Met216=)
3g.129532368G>ACA354469956RHOc.648G>A (p.Met216Ile)
3g.129532368G>CCA354469958RHOc.648G>C (p.Met216Ile)
3g.129532368G>TCA354469957RHOc.648G>T (p.Met216Ile)
3g.129532369A=CA1401211269RHOc.649A= (p.Ile217=)
3g.129532369A>CCA354469961RHOc.649A>C (p.Ile217Leu)
3g.129532369A>GCA354469964RHOc.649A>G (p.Ile217Val)
dbSNP gnomAD v2 gnomAD v4
3g.129532369A>TCA354469962RHOc.649A>T (p.Ile217Phe)
ClinVar dbSNP gnomAD v4
3g.129532370T>ACA354469965RHOc.650T>A (p.Ile217Asn)
3g.129532370T>CCA354469970RHOc.650T>C (p.Ile217Thr)
3g.129532370T>GCA354469968RHOc.650T>G (p.Ile217Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129532370T=CA1401211272RHOc.650T= (p.Ile217=)
3g.129532372_129532379dupCA2667616977RHOc.652_659dup (p.Phe220LeufsTer?)
gnomAD v4
3g.129532371T>ACA435769008RHOc.651T>A (p.Ile217=)
3g.129532371T>CCA435769009RHOc.651T>C (p.Ile217=)
dbSNP gnomAD v4
3g.129532371T>GCA354469971RHOc.651T>G (p.Ile217Met)
3g.129532371T=CA1401211274RHOc.651T= (p.Ile217=)
3g.129532372A>CCA354469973RHOc.652A>C (p.Ile218Leu)
3g.129532372A>GCA354469975RHOc.652A>G (p.Ile218Val)
dbSNP
3g.129532372A>TCA354469976RHOc.652A>T (p.Ile218Phe)
3g.129532373T>ACA354469978RHOc.653T>A (p.Ile218Asn)
3g.129532373T>CCA354469980RHOc.653T>C (p.Ile218Thr)
gnomAD v4
3g.129532373T>GCA354469981RHOc.653T>G (p.Ile218Ser)
3g.129532374C>ACA435769010RHOc.654C>A (p.Ile218=)
3g.129532374C>GCA354469983RHOc.654C>G (p.Ile218Met)
3g.129532374C>TCA435769011RHOc.654C>T (p.Ile218=)
3g.129532375A>CCA354469984RHOc.655A>C (p.Ile219Leu)
3g.129532375A>GCA354469986RHOc.655A>G (p.Ile219Val)
3g.129532375A>TCA354469988RHOc.655A>T (p.Ile219Phe)
3g.129532376T>ACA354469990RHOc.656T>A (p.Ile219Asn)
3g.129532376T>CCA354469993RHOc.656T>C (p.Ile219Thr)
gnomAD v4
3g.129532376T>GCA354469992RHOc.656T>G (p.Ile219Ser)
3g.129532377C>ACA435769012RHOc.657C>A (p.Ile219=)
COSMIC
3g.129532377C>GCA354469995RHOc.657C>G (p.Ile219Met)
3g.129532377C>TCA435769013RHOc.657C>T (p.Ile219=)
3g.129532378T>ACA354469996RHOc.658T>A (p.Phe220Ile)
3g.129532378T>CCA354469998RHOc.658T>C (p.Phe220Leu)
3g.129532378T>GCA354470000RHOc.658T>G (p.Phe220Val)
3g.129532379T>ACA354470001RHOc.659T>A (p.Phe220Tyr)
3g.129532379T>CCA354470002RHOc.659T>C (p.Phe220Ser)
3g.129532379T>GCA2607232RHOc.659T>G (p.Phe220Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532379T=CA1401211276RHOc.659T= (p.Phe220=)
3g.129532380T>ACA354470004RHOc.660T>A (p.Phe220Leu)
3g.129532380T>CCA435769014RHOc.660T>C (p.Phe220=)
dbSNP
3g.129532380T>GCA2607233RHOc.660T>G (p.Phe220Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532380T=CA1401211278RHOc.660T= (p.Phe220=)
3g.129532381T>ACA354470008RHOc.661T>A (p.Phe221Ile)
gnomAD v4
3g.129532381T>CCA354470009RHOc.661T>C (p.Phe221Leu)
3g.129532381T>GCA354470006RHOc.661T>G (p.Phe221Val)
3g.129532382T>ACA354470010RHOc.662T>A (p.Phe221Tyr)
3g.129532382T>CCA354470011RHOc.662T>C (p.Phe221Ser)
3g.129532382T>GCA354470013RHOc.662T>G (p.Phe221Cys)
3g.129532383C>ACA354470014RHOc.663C>A (p.Phe221Leu)
3g.129532383C>GCA354470015RHOc.663C>G (p.Phe221Leu)
3g.129532383C>TCA435769015RHOc.663C>T (p.Phe221=)
3g.129532384T>ACA354470019RHOc.664T>A (p.Cys222Ser)
3g.129532384T>CCA354470016RHOc.664T>C (p.Cys222Arg)
3g.129532384T>GCA354470018RHOc.664T>G (p.Cys222Gly)
3g.129532385G>ACA354470021RHOc.665G>A (p.Cys222Tyr)
3g.129532385G>CCA354470023RHOc.665G>C (p.Cys222Ser)
3g.129532385G>TCA354470024RHOc.665G>T (p.Cys222Phe)
3g.129532386C>ACA354470026RHOc.666C>A (p.Cys222Ter)
3g.129532386C>GCA354470028RHOc.666C>G (p.Cys222Trp)
3g.129532386C>TCA435769016RHOc.666C>T (p.Cys222=)
3g.129532387T>ACA354470030RHOc.667T>A (p.Tyr223Asn)
3g.129532387T>CCA354470033RHOc.667T>C (p.Tyr223His)
3g.129532387T>GCA354470031RHOc.667T>G (p.Tyr223Asp)
3g.129532388A>CCA354470034RHOc.668A>C (p.Tyr223Ser)
3g.129532388A>GCA354470036RHOc.668A>G (p.Tyr223Cys)
3g.129532388A>TCA354470037RHOc.668A>T (p.Tyr223Phe)
3g.129532389T>ACA354470038RHOc.669T>A (p.Tyr223Ter)
3g.129532389T>CCA435769017RHOc.669T>C (p.Tyr223=)
gnomAD v4
3g.129532389T>GCA354470039RHOc.669T>G (p.Tyr223Ter)
3g.129532390G>ACA354470040RHOc.670G>A (p.Gly224Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129532390G>CCA2607234RHOc.670G>C (p.Gly224Arg)
dbSNP ExAC gnomAD v2 COSMIC
3g.129532390G=CA1401211280RHOc.670G= (p.Gly224=)
3g.129532390G>TCA354470042RHOc.670G>T (p.Gly224Trp)
3g.129532391G>ACA2607235RHOc.671G>A (p.Gly224Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532391G>CCA354470044RHOc.671G>C (p.Gly224Ala)
3g.129532391G=CA1401211282RHOc.671G= (p.Gly224=)
3g.129532391G>TCA354470045RHOc.671G>T (p.Gly224Val)
3g.129532392G>ACA435769018RHOc.672G>A (p.Gly224=)
3g.129532392G>CCA435769019RHOc.672G>C (p.Gly224=)
3g.129532392G>TCA435769020RHOc.672G>T (p.Gly224=)
3g.129532393C>ACA354470050RHOc.673C>A (p.Gln225Lys)
gnomAD v4
3g.129532393C=CA1401211285RHOc.673C= (p.Gln225=)
3g.129532393C>GCA354470048RHOc.673C>G (p.Gln225Glu)
3g.129532393C>TCA2607236RHOc.673C>T (p.Gln225Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532394A>CCA354470051RHOc.674A>C (p.Gln225Pro)
3g.129532394A>GCA354470053RHOc.674A>G (p.Gln225Arg)
3g.129532394A>TCA354470054RHOc.674A>T (p.Gln225Leu)
3g.129532395G>ACA435769021RHOc.675G>A (p.Gln225=)
gnomAD v4
3g.129532395G>CCA354470055RHOc.675G>C (p.Gln225His)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129532395G=CA1401211288RHOc.675G= (p.Gln225=)
3g.129532395G>TCA354470056RHOc.675G>T (p.Gln225His)
3g.129532396C>ACA354470057RHOc.676C>A (p.Leu226Ile)
3g.129532396C>GCA354470059RHOc.676C>G (p.Leu226Val)
3g.129532396C>TCA354470060RHOc.676C>T (p.Leu226Phe)
3g.129532397T>ACA354470062RHOc.677T>A (p.Leu226His)
3g.129532397T>CCA354470065RHOc.677T>C (p.Leu226Pro)
ClinVar dbSNP
3g.129532397T>GCA354470064RHOc.677T>G (p.Leu226Arg)
3g.129532397T=CA1401211290RHOc.677T= (p.Leu226=)
3g.129532398C>ACA435769022RHOc.678C>A (p.Leu226=)
3g.129532398C=CA1401211293RHOc.678C= (p.Leu226=)
3g.129532398C>GCA82620581RHOc.678C>G (p.Leu226=)
dbSNP
3g.129532398C>TCA2607237RHOc.678C>T (p.Leu226=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
3g.129532399G>ACA2607238RHOc.679G>A (p.Val227Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532399G>CCA354470069RHOc.679G>C (p.Val227Leu)
3g.129532399G=CA1401211296RHOc.679G= (p.Val227=)
3g.129532399G>TCA354470070RHOc.679G>T (p.Val227Phe)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129532400T>ACA354470072RHOc.680T>A (p.Val227Asp)
3g.129532400T>CCA354470075RHOc.680T>C (p.Val227Ala)
dbSNP gnomAD v3 gnomAD v4
3g.129532400T>GCA354470074RHOc.680T>G (p.Val227Gly)
dbSNP gnomAD v2 gnomAD v4
3g.129532400T=CA1401211298RHOc.680T= (p.Val227=)
3g.129532401C>ACA435769023RHOc.681C>A (p.Val227=)
3g.129532401C>GCA435769024RHOc.681C>G (p.Val227=)
3g.129532401C>TCA435769025RHOc.681C>T (p.Val227=)
ClinVar gnomAD v4
3g.129532402T>ACA354470077RHOc.682T>A (p.Phe228Ile)
3g.129532402T>CCA354470079RHOc.682T>C (p.Phe228Leu)
3g.129532402T>GCA354470080RHOc.682T>G (p.Phe228Val)
3g.129532403T>ACA354470082RHOc.683T>A (p.Phe228Tyr)
3g.129532403T>CCA354470083RHOc.683T>C (p.Phe228Ser)
ClinVar dbSNP gnomAD v4
3g.129532403T>GCA354470085RHOc.683T>G (p.Phe228Cys)
gnomAD v4
3g.129532403T=CA1401211300RHOc.683T= (p.Phe228=)
3g.129532404C>ACA354470087RHOc.684C>A (p.Phe228Leu)
3g.129532404C=CA1401211302RHOc.684C= (p.Phe228=)
3g.129532404C>GCA354470089RHOc.684C>G (p.Phe228Leu)
3g.129532404C>TCA435769026RHOc.684C>T (p.Phe228=)
dbSNP
3g.129532405A>CCA354470090RHOc.685A>C (p.Thr229Pro)
3g.129532405A>GCA354470093RHOc.685A>G (p.Thr229Ala)
3g.129532405A>TCA354470094RHOc.685A>T (p.Thr229Ser)
3g.129532406C>ACA354470095RHOc.686C>A (p.Thr229Asn)
3g.129532406C>GCA354470098RHOc.686C>G (p.Thr229Ser)
3g.129532406C>TCA354470097RHOc.686C>T (p.Thr229Ile)
gnomAD v4

Number of alleles fetched