Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.148741452A>CCA436389769AGTR1c.417A>C (p.Arg139=)
c.504A>C (p.Arg168=)
c.522A>C (p.Arg174=)
3g.148741452A>GCA436389768AGTR1c.417A>G (p.Arg139=)
c.504A>G (p.Arg168=)
c.522A>G (p.Arg174=)
3g.148741452A>TCA436389767AGTR1c.417A>T (p.Arg139=)
c.504A>T (p.Arg168=)
c.522A>T (p.Arg174=)
3g.148741453C>ACA354887285AGTR1c.418C>A (p.Arg140Ser)
c.505C>A (p.Arg169Ser)
c.523C>A (p.Arg175Ser)
3g.148741453C=CA1409909705AGTR1c.418C= (p.Arg140=)
c.505C= (p.Arg169=)
c.523C= (p.Arg175=)
3g.148741453C>GCA354887289AGTR1c.418C>G (p.Arg140Gly)
c.505C>G (p.Arg169Gly)
c.523C>G (p.Arg175Gly)
 dbSNP
3g.148741453C>TCA2657329AGTR1c.418C>T (p.Arg140Cys)
c.505C>T (p.Arg169Cys)
c.523C>T (p.Arg175Cys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.148741454G>ACA2657330AGTR1c.419G>A (p.Arg140His)
c.506G>A (p.Arg169His)
c.524G>A (p.Arg175His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.148741454G>CCA354887301AGTR1c.419G>C (p.Arg140Pro)
c.506G>C (p.Arg169Pro)
c.524G>C (p.Arg175Pro)
3g.148741454G=CA1409909707AGTR1c.419G= (p.Arg140=)
c.506G= (p.Arg169=)
c.524G= (p.Arg175=)
3g.148741454G>TCA354887296AGTR1c.419G>T (p.Arg140Leu)
c.506G>T (p.Arg169Leu)
c.524G>T (p.Arg175Leu)
 gnomAD v4
3g.148741455C>ACA436389774AGTR1c.420C>A (p.Arg140=)
c.507C>A (p.Arg169=)
c.525C>A (p.Arg175=)
3g.148741455C>GCA436389775AGTR1c.420C>G (p.Arg140=)
c.507C>G (p.Arg169=)
c.525C>G (p.Arg175=)
3g.148741455C>TCA436389776AGTR1c.420C>T (p.Arg140=)
c.507C>T (p.Arg169=)
c.525C>T (p.Arg175=)
 COSMIC
3g.148741456A>CCA354887313AGTR1c.421A>C (p.Thr141Pro)
c.508A>C (p.Thr170Pro)
c.526A>C (p.Thr176Pro)
3g.148741456A>GCA354887314AGTR1c.421A>G (p.Thr141Ala)
c.508A>G (p.Thr170Ala)
c.526A>G (p.Thr176Ala)
3g.148741456A>TCA354887315AGTR1c.421A>T (p.Thr141Ser)
c.508A>T (p.Thr170Ser)
c.526A>T (p.Thr176Ser)
3g.148741457C>ACA354887317AGTR1c.422C>A (p.Thr141Lys)
c.509C>A (p.Thr170Lys)
c.527C>A (p.Thr176Lys)
3g.148741457C>GCA354887319AGTR1c.422C>G (p.Thr141Arg)
c.509C>G (p.Thr170Arg)
c.527C>G (p.Thr176Arg)
3g.148741457C>TCA354887321AGTR1c.422C>T (p.Thr141Ile)
c.509C>T (p.Thr170Ile)
c.527C>T (p.Thr176Ile)
3g.148741458A>CCA436389782AGTR1c.423A>C (p.Thr141=)
c.510A>C (p.Thr170=)
c.528A>C (p.Thr176=)
3g.148741458A>GCA436389784AGTR1c.423A>G (p.Thr141=)
c.510A>G (p.Thr170=)
c.528A>G (p.Thr176=)
3g.148741458A>TCA436389783AGTR1c.423A>T (p.Thr141=)
c.510A>T (p.Thr170=)
c.528A>T (p.Thr176=)
3g.148741459A>CCA354887324AGTR1c.424A>C (p.Met142Leu)
c.511A>C (p.Met171Leu)
c.529A>C (p.Met177Leu)
3g.148741459A>GCA354887328AGTR1c.424A>G (p.Met142Val)
c.511A>G (p.Met171Val)
c.529A>G (p.Met177Val)
 gnomAD v4
3g.148741459A>TCA354887332AGTR1c.424A>T (p.Met142Leu)
c.511A>T (p.Met171Leu)
c.529A>T (p.Met177Leu)
3g.148741460T>ACA354887333AGTR1c.425T>A (p.Met142Lys)
c.512T>A (p.Met171Lys)
c.530T>A (p.Met177Lys)
3g.148741460T>CCA354887334AGTR1c.425T>C (p.Met142Thr)
c.512T>C (p.Met171Thr)
c.530T>C (p.Met177Thr)
3g.148741460T>GCA354887335AGTR1c.425T>G (p.Met142Arg)
c.512T>G (p.Met171Arg)
c.530T>G (p.Met177Arg)
3g.148741461G>ACA354887343AGTR1c.426G>A (p.Met142Ile)
c.513G>A (p.Met171Ile)
c.531G>A (p.Met177Ile)
 gnomAD v4
3g.148741461G>CCA354887337AGTR1c.426G>C (p.Met142Ile)
c.513G>C (p.Met171Ile)
c.531G>C (p.Met177Ile)
3g.148741461G>TCA354887336AGTR1c.426G>T (p.Met142Ile)
c.513G>T (p.Met171Ile)
c.531G>T (p.Met177Ile)
3g.148741462C>ACA2657331AGTR1c.427C>A (p.Leu143Ile)
c.514C>A (p.Leu172Ile)
c.532C>A (p.Leu178Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741462C=CA1409909714AGTR1c.427C= (p.Leu143=)
c.514C= (p.Leu172=)
c.532C= (p.Leu178=)
3g.148741462C>GCA354887349AGTR1c.427C>G (p.Leu143Val)
c.514C>G (p.Leu172Val)
c.532C>G (p.Leu178Val)
3g.148741462C>TCA354887359AGTR1c.427C>T (p.Leu143Phe)
c.514C>T (p.Leu172Phe)
c.532C>T (p.Leu178Phe)
 gnomAD v4
3g.148741463T>ACA354887360AGTR1c.428T>A (p.Leu143His)
c.515T>A (p.Leu172His)
c.533T>A (p.Leu178His)
3g.148741463T>CCA354887361AGTR1c.428T>C (p.Leu143Pro)
c.515T>C (p.Leu172Pro)
c.533T>C (p.Leu178Pro)
 gnomAD v4
3g.148741463T>GCA354887362AGTR1c.428T>G (p.Leu143Arg)
c.515T>G (p.Leu172Arg)
c.533T>G (p.Leu178Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.148741463T=CA1409909724AGTR1c.428T= (p.Leu143=)
c.515T= (p.Leu172=)
c.533T= (p.Leu178=)
3g.148741464T>ACA436389789AGTR1c.429T>A (p.Leu143=)
c.516T>A (p.Leu172=)
c.534T>A (p.Leu178=)
3g.148741464T>CCA436389796AGTR1c.429T>C (p.Leu143=)
c.516T>C (p.Leu172=)
c.534T>C (p.Leu178=)
 dbSNP gnomAD v2 gnomAD v4
3g.148741464T>GCA2657332AGTR1c.429T>G (p.Leu143=)
c.516T>G (p.Leu172=)
c.534T>G (p.Leu178=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741464T=CA1409909728AGTR1c.429T= (p.Leu143=)
c.516T= (p.Leu172=)
c.534T= (p.Leu178=)
3g.148741465G>ACA354887368AGTR1c.430G>A (p.Val144Ile)
c.517G>A (p.Val173Ile)
c.535G>A (p.Val179Ile)
 dbSNP gnomAD v2 gnomAD v4
3g.148741465G>CCA354887369AGTR1c.430G>C (p.Val144Leu)
c.517G>C (p.Val173Leu)
c.535G>C (p.Val179Leu)
3g.148741465G=CA1409909731AGTR1c.430G= (p.Val144=)
c.517G= (p.Val173=)
c.535G= (p.Val179=)
3g.148741465G>TCA354887372AGTR1c.430G>T (p.Val144Leu)
c.517G>T (p.Val173Leu)
c.535G>T (p.Val179Leu)
3g.148741466T>ACA354887373AGTR1c.431T>A (p.Val144Glu)
c.518T>A (p.Val173Glu)
c.536T>A (p.Val179Glu)
3g.148741466T>CCA354887375AGTR1c.431T>C (p.Val144Ala)
c.518T>C (p.Val173Ala)
c.536T>C (p.Val179Ala)
 gnomAD v4
3g.148741466T>GCA354887389AGTR1c.431T>G (p.Val144Gly)
c.518T>G (p.Val173Gly)
c.536T>G (p.Val179Gly)
3g.148741467A>CCA436389800AGTR1c.432A>C (p.Val144=)
c.519A>C (p.Val173=)
c.537A>C (p.Val179=)
3g.148741467A>GCA436389802AGTR1c.432A>G (p.Val144=)
c.519A>G (p.Val173=)
c.537A>G (p.Val179=)
3g.148741467A>TCA436389804AGTR1c.432A>T (p.Val144=)
c.519A>T (p.Val173=)
c.537A>T (p.Val179=)
3g.148741468G>ACA354887420AGTR1c.433G>A (p.Ala145Thr)
c.520G>A (p.Ala174Thr)
c.538G>A (p.Ala180Thr)
 gnomAD v4
3g.148741468G>CCA354887392AGTR1c.433G>C (p.Ala145Pro)
c.520G>C (p.Ala174Pro)
c.538G>C (p.Ala180Pro)
3g.148741468G>TCA354887415AGTR1c.433G>T (p.Ala145Ser)
c.520G>T (p.Ala174Ser)
c.538G>T (p.Ala180Ser)
 gnomAD v4
3g.148741469C>ACA354887422AGTR1c.434C>A (p.Ala145Asp)
c.521C>A (p.Ala174Asp)
c.539C>A (p.Ala180Asp)
3g.148741469C>GCA354887424AGTR1c.434C>G (p.Ala145Gly)
c.521C>G (p.Ala174Gly)
c.539C>G (p.Ala180Gly)
3g.148741469C>TCA354887427AGTR1c.434C>T (p.Ala145Val)
c.521C>T (p.Ala174Val)
c.539C>T (p.Ala180Val)
 gnomAD v4
3g.148741470C>ACA436389808AGTR1c.435C>A (p.Ala145=)
c.522C>A (p.Ala174=)
c.540C>A (p.Ala180=)
3g.148741470C=CA1409909733AGTR1c.435C= (p.Ala145=)
c.522C= (p.Ala174=)
c.540C= (p.Ala180=)
3g.148741470C>GCA2657333AGTR1c.435C>G (p.Ala145=)
c.522C>G (p.Ala174=)
c.540C>G (p.Ala180=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741470C>TCA436389811AGTR1c.435C>T (p.Ala145=)
c.522C>T (p.Ala174=)
c.540C>T (p.Ala180=)
 gnomAD v4
3g.148741471A>CCA354887443AGTR1c.436A>C (p.Lys146Gln)
c.523A>C (p.Lys175Gln)
c.541A>C (p.Lys181Gln)
3g.148741471A>GCA354887444AGTR1c.436A>G (p.Lys146Glu)
c.523A>G (p.Lys175Glu)
c.541A>G (p.Lys181Glu)
 gnomAD v4
3g.148741471A>TCA354887447AGTR1c.436A>T (p.Lys146Ter)
c.523A>T (p.Lys175Ter)
c.541A>T (p.Lys181Ter)
 gnomAD v4
3g.148741472A>CCA354887449AGTR1c.437A>C (p.Lys146Thr)
c.524A>C (p.Lys175Thr)
c.542A>C (p.Lys181Thr)
3g.148741472A>GCA354887451AGTR1c.437A>G (p.Lys146Arg)
c.524A>G (p.Lys175Arg)
c.542A>G (p.Lys181Arg)
3g.148741472A>TCA354887453AGTR1c.437A>T (p.Lys146Ile)
c.524A>T (p.Lys175Ile)
c.542A>T (p.Lys181Ile)
3g.148741473A>CCA354887458AGTR1c.438A>C (p.Lys146Asn)
c.525A>C (p.Lys175Asn)
c.543A>C (p.Lys181Asn)
3g.148741473A>GCA436389813AGTR1c.438A>G (p.Lys146=)
c.525A>G (p.Lys175=)
c.543A>G (p.Lys181=)
3g.148741473A>TCA354887460AGTR1c.438A>T (p.Lys146Asn)
c.525A>T (p.Lys175Asn)
c.543A>T (p.Lys181Asn)
3g.148741474G>ACA354887464AGTR1c.439G>A (p.Val147Ile)
c.526G>A (p.Val176Ile)
c.544G>A (p.Val182Ile)
3g.148741474G>CCA354887463AGTR1c.439G>C (p.Val147Leu)
c.526G>C (p.Val176Leu)
c.544G>C (p.Val182Leu)
3g.148741474G>TCA354887462AGTR1c.439G>T (p.Val147Phe)
c.526G>T (p.Val176Phe)
c.544G>T (p.Val182Phe)
 COSMIC
3g.148741475T>ACA354887470AGTR1c.440T>A (p.Val147Asp)
c.527T>A (p.Val176Asp)
c.545T>A (p.Val182Asp)
3g.148741475T>CCA354887468AGTR1c.440T>C (p.Val147Ala)
c.527T>C (p.Val176Ala)
c.545T>C (p.Val182Ala)
3g.148741475T>GCA354887471AGTR1c.440T>G (p.Val147Gly)
c.527T>G (p.Val176Gly)
c.545T>G (p.Val182Gly)
3g.148741476C>ACA436389815AGTR1c.441C>A (p.Val147=)
c.528C>A (p.Val176=)
c.546C>A (p.Val182=)
3g.148741476C>GCA436389816AGTR1c.441C>G (p.Val147=)
c.528C>G (p.Val176=)
c.546C>G (p.Val182=)
3g.148741476C>TCA436389822AGTR1c.441C>T (p.Val147=)
c.528C>T (p.Val176=)
c.546C>T (p.Val182=)
 gnomAD v4
3g.148741477A>CCA354887472AGTR1c.442A>C (p.Thr148Pro)
c.529A>C (p.Thr177Pro)
c.547A>C (p.Thr183Pro)
3g.148741477A>GCA354887476AGTR1c.442A>G (p.Thr148Ala)
c.529A>G (p.Thr177Ala)
c.547A>G (p.Thr183Ala)
3g.148741477A>TCA354887474AGTR1c.442A>T (p.Thr148Ser)
c.529A>T (p.Thr177Ser)
c.547A>T (p.Thr183Ser)
3g.148741478C>ACA354887479AGTR1c.443C>A (p.Thr148Asn)
c.530C>A (p.Thr177Asn)
c.548C>A (p.Thr183Asn)
3g.148741478C>GCA354887483AGTR1c.443C>G (p.Thr148Ser)
c.530C>G (p.Thr177Ser)
c.548C>G (p.Thr183Ser)
3g.148741478C>TCA354887481AGTR1c.443C>T (p.Thr148Ile)
c.530C>T (p.Thr177Ile)
c.548C>T (p.Thr183Ile)
 COSMIC
3g.148741479C>ACA436389836AGTR1c.444C>A (p.Thr148=)
c.531C>A (p.Thr177=)
c.549C>A (p.Thr183=)
3g.148741479C=CA1409909737AGTR1c.444C= (p.Thr148=)
c.531C= (p.Thr177=)
c.549C= (p.Thr183=)
3g.148741479C>GCA436389833AGTR1c.444C>G (p.Thr148=)
c.531C>G (p.Thr177=)
c.549C>G (p.Thr183=)
3g.148741479C>TCA2657334AGTR1c.444C>T (p.Thr148=)
c.531C>T (p.Thr177=)
c.549C>T (p.Thr183=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741480T>ACA354887487AGTR1c.445T>A (p.Cys149Ser)
c.532T>A (p.Cys178Ser)
c.550T>A (p.Cys184Ser)
3g.148741480T>CCA354887490AGTR1c.445T>C (p.Cys149Arg)
c.532T>C (p.Cys178Arg)
c.550T>C (p.Cys184Arg)
3g.148741480T>GCA354887504AGTR1c.445T>G (p.Cys149Gly)
c.532T>G (p.Cys178Gly)
c.550T>G (p.Cys184Gly)
3g.148741481G>ACA85497729AGTR1c.446G>A (p.Cys149Tyr)
c.533G>A (p.Cys178Tyr)
c.551G>A (p.Cys184Tyr)
 dbSNP
3g.148741481G>CCA354887510AGTR1c.446G>C (p.Cys149Ser)
c.533G>C (p.Cys178Ser)
c.551G>C (p.Cys184Ser)
3g.148741481G=CA1409909742AGTR1c.446G= (p.Cys149=)
c.533G= (p.Cys178=)
c.551G= (p.Cys184=)
3g.148741481G>TCA354887512AGTR1c.446G>T (p.Cys149Phe)
c.533G>T (p.Cys178Phe)
c.551G>T (p.Cys184Phe)
 gnomAD v4
3g.148741482C>ACA354887517AGTR1c.447C>A (p.Cys149Ter)
c.534C>A (p.Cys178Ter)
c.552C>A (p.Cys184Ter)
3g.148741482C>GCA354887520AGTR1c.447C>G (p.Cys149Trp)
c.534C>G (p.Cys178Trp)
c.552C>G (p.Cys184Trp)
3g.148741482C>TCA436389839AGTR1c.447C>T (p.Cys149=)
c.534C>T (p.Cys178=)
c.552C>T (p.Cys184=)
3g.148741483A=CA1409909746AGTR1c.448A= (p.Ile150=)
c.535A= (p.Ile179=)
c.553A= (p.Ile185=)
3g.148741483A>CCA354887523AGTR1c.448A>C (p.Ile150Leu)
c.535A>C (p.Ile179Leu)
c.553A>C (p.Ile185Leu)
 dbSNP gnomAD v2 gnomAD v4
3g.148741483A>GCA354887524AGTR1c.448A>G (p.Ile150Val)
c.535A>G (p.Ile179Val)
c.553A>G (p.Ile185Val)
 gnomAD v4
3g.148741483A>TCA354887529AGTR1c.448A>T (p.Ile150Phe)
c.535A>T (p.Ile179Phe)
c.553A>T (p.Ile185Phe)
3g.148741484T>ACA354887541AGTR1c.449T>A (p.Ile150Asn)
c.536T>A (p.Ile179Asn)
c.554T>A (p.Ile185Asn)
3g.148741484T>CCA354887532AGTR1c.449T>C (p.Ile150Thr)
c.536T>C (p.Ile179Thr)
c.554T>C (p.Ile185Thr)
3g.148741484T>GCA354887536AGTR1c.449T>G (p.Ile150Ser)
c.536T>G (p.Ile179Ser)
c.554T>G (p.Ile185Ser)
3g.148741485C>ACA436389845AGTR1c.450C>A (p.Ile150=)
c.537C>A (p.Ile179=)
c.555C>A (p.Ile185=)
3g.148741485C=CA1409909749AGTR1c.450C= (p.Ile150=)
c.537C= (p.Ile179=)
c.555C= (p.Ile185=)
3g.148741485C>GCA354887544AGTR1c.450C>G (p.Ile150Met)
c.537C>G (p.Ile179Met)
c.555C>G (p.Ile185Met)
 dbSNP gnomAD v2 gnomAD v4
3g.148741485C>TCA436389846AGTR1c.450C>T (p.Ile150=)
c.537C>T (p.Ile179=)
c.555C>T (p.Ile185=)
3g.148741486A>CCA354887546AGTR1c.451A>C (p.Ile151Leu)
c.538A>C (p.Ile180Leu)
c.556A>C (p.Ile186Leu)
3g.148741486A>GCA354887550AGTR1c.451A>G (p.Ile151Val)
c.538A>G (p.Ile180Val)
c.556A>G (p.Ile186Val)
 gnomAD v4
3g.148741486A>TCA354887554AGTR1c.451A>T (p.Ile151Phe)
c.538A>T (p.Ile180Phe)
c.556A>T (p.Ile186Phe)
3g.148741487T>ACA354887558AGTR1c.452T>A (p.Ile151Asn)
c.539T>A (p.Ile180Asn)
c.557T>A (p.Ile186Asn)
3g.148741487T>CCA354887561AGTR1c.452T>C (p.Ile151Thr)
c.539T>C (p.Ile180Thr)
c.557T>C (p.Ile186Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.148741487T>GCA354887563AGTR1c.452T>G (p.Ile151Ser)
c.539T>G (p.Ile180Ser)
c.557T>G (p.Ile186Ser)
3g.148741487T=CA1409909751AGTR1c.452T= (p.Ile151=)
c.539T= (p.Ile180=)
c.557T= (p.Ile186=)
3g.148741488C>ACA436389852AGTR1c.453C>A (p.Ile151=)
c.540C>A (p.Ile180=)
c.558C>A (p.Ile186=)
3g.148741488C=CA1409909753AGTR1c.453C= (p.Ile151=)
c.540C= (p.Ile180=)
c.558C= (p.Ile186=)
3g.148741488C>GCA354887565AGTR1c.453C>G (p.Ile151Met)
c.540C>G (p.Ile180Met)
c.558C>G (p.Ile186Met)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.148741488C>TCA436389854AGTR1c.453C>T (p.Ile151=)
c.540C>T (p.Ile180=)
c.558C>T (p.Ile186=)
 COSMIC
3g.148741489A>CCA354887568AGTR1c.454A>C (p.Ile152Leu)
c.541A>C (p.Ile181Leu)
c.559A>C (p.Ile187Leu)
3g.148741489A>GCA354887570AGTR1c.454A>G (p.Ile152Val)
c.541A>G (p.Ile181Val)
c.559A>G (p.Ile187Val)
3g.148741489A>TCA354887573AGTR1c.454A>T (p.Ile152Phe)
c.541A>T (p.Ile181Phe)
c.559A>T (p.Ile187Phe)
3g.148741490T>ACA354887590AGTR1c.455T>A (p.Ile152Asn)
c.542T>A (p.Ile181Asn)
c.560T>A (p.Ile187Asn)
3g.148741490T>CCA354887581AGTR1c.455T>C (p.Ile152Thr)
c.542T>C (p.Ile181Thr)
c.560T>C (p.Ile187Thr)
3g.148741490T>GCA354887578AGTR1c.455T>G (p.Ile152Ser)
c.542T>G (p.Ile181Ser)
c.560T>G (p.Ile187Ser)
3g.148741491T>ACA436389857AGTR1c.456T>A (p.Ile152=)
c.543T>A (p.Ile181=)
c.561T>A (p.Ile187=)
3g.148741491T>CCA436389859AGTR1c.456T>C (p.Ile152=)
c.543T>C (p.Ile181=)
c.561T>C (p.Ile187=)
3g.148741491T>GCA354887592AGTR1c.456T>G (p.Ile152Met)
c.543T>G (p.Ile181Met)
c.561T>G (p.Ile187Met)
 gnomAD v4
3g.148741492T>ACA354887595AGTR1c.457T>A (p.Trp153Arg)
c.544T>A (p.Trp182Arg)
c.562T>A (p.Trp188Arg)
3g.148741492T>CCA354887597AGTR1c.457T>C (p.Trp153Arg)
c.544T>C (p.Trp182Arg)
c.562T>C (p.Trp188Arg)
3g.148741492T>GCA354887600AGTR1c.457T>G (p.Trp153Gly)
c.544T>G (p.Trp182Gly)
c.562T>G (p.Trp188Gly)
3g.148741493G>ACA354887603AGTR1c.458G>A (p.Trp153Ter)
c.545G>A (p.Trp182Ter)
c.563G>A (p.Trp188Ter)
3g.148741493G>CCA354887605AGTR1c.458G>C (p.Trp153Ser)
c.545G>C (p.Trp182Ser)
c.563G>C (p.Trp188Ser)
3g.148741493G>TCA354887608AGTR1c.458G>T (p.Trp153Leu)
c.545G>T (p.Trp182Leu)
c.563G>T (p.Trp188Leu)
 gnomAD v4
3g.148741494G>ACA354887611AGTR1c.459G>A (p.Trp153Ter)
c.546G>A (p.Trp182Ter)
c.564G>A (p.Trp188Ter)
 gnomAD v4
3g.148741494G>CCA354887612AGTR1c.459G>C (p.Trp153Cys)
c.546G>C (p.Trp182Cys)
c.564G>C (p.Trp188Cys)
3g.148741494G>TCA354887615AGTR1c.459G>T (p.Trp153Cys)
c.546G>T (p.Trp182Cys)
c.564G>T (p.Trp188Cys)
3g.148741495C>ACA354887618AGTR1c.460C>A (p.Leu154Met)
c.547C>A (p.Leu183Met)
c.565C>A (p.Leu189Met)
3g.148741495C>GCA354887621AGTR1c.460C>G (p.Leu154Val)
c.547C>G (p.Leu183Val)
c.565C>G (p.Leu189Val)
3g.148741495C>TCA436389867AGTR1c.460C>T (p.Leu154=)
c.547C>T (p.Leu183=)
c.565C>T (p.Leu189=)
3g.148741496T>ACA354887624AGTR1c.461T>A (p.Leu154Gln)
c.548T>A (p.Leu183Gln)
c.566T>A (p.Leu189Gln)
3g.148741496T>CCA354887625AGTR1c.461T>C (p.Leu154Pro)
c.548T>C (p.Leu183Pro)
c.566T>C (p.Leu189Pro)
3g.148741496T>GCA354887628AGTR1c.461T>G (p.Leu154Arg)
c.548T>G (p.Leu183Arg)
c.566T>G (p.Leu189Arg)
3g.148741497G>ACA436389870AGTR1c.462G>A (p.Leu154=)
c.549G>A (p.Leu183=)
c.567G>A (p.Leu189=)
3g.148741497G>CCA436389871AGTR1c.462G>C (p.Leu154=)
c.549G>C (p.Leu183=)
c.567G>C (p.Leu189=)
 dbSNP
3g.148741497G=CA1409909756AGTR1c.462G= (p.Leu154=)
c.549G= (p.Leu183=)
c.567G= (p.Leu189=)
3g.148741497G>TCA436389872AGTR1c.462G>T (p.Leu154=)
c.549G>T (p.Leu183=)
c.567G>T (p.Leu189=)
3g.148741498C>ACA354887630AGTR1c.463C>A (p.Leu155Met)
c.550C>A (p.Leu184Met)
c.568C>A (p.Leu190Met)
3g.148741498C>GCA354887631AGTR1c.463C>G (p.Leu155Val)
c.550C>G (p.Leu184Val)
c.568C>G (p.Leu190Val)
3g.148741498C>TCA436389874AGTR1c.463C>T (p.Leu155=)
c.550C>T (p.Leu184=)
c.568C>T (p.Leu190=)
3g.148741499T>ACA354887633AGTR1c.464T>A (p.Leu155Gln)
c.551T>A (p.Leu184Gln)
c.569T>A (p.Leu190Gln)
3g.148741499T>CCA354887636AGTR1c.464T>C (p.Leu155Pro)
c.551T>C (p.Leu184Pro)
c.569T>C (p.Leu190Pro)
3g.148741499T>GCA354887639AGTR1c.464T>G (p.Leu155Arg)
c.551T>G (p.Leu184Arg)
c.569T>G (p.Leu190Arg)
3g.148741500G>ACA436389884AGTR1c.465G>A (p.Leu155=)
c.552G>A (p.Leu184=)
c.570G>A (p.Leu190=)
3g.148741500G>CCA436389882AGTR1c.465G>C (p.Leu155=)
c.552G>C (p.Leu184=)
c.570G>C (p.Leu190=)
3g.148741500G>TCA436389881AGTR1c.465G>T (p.Leu155=)
c.552G>T (p.Leu184=)
c.570G>T (p.Leu190=)
3g.148741501G>ACA2657335AGTR1c.466G>A (p.Ala156Thr)
c.553G>A (p.Ala185Thr)
c.571G>A (p.Ala191Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741501G>CCA354887644AGTR1c.466G>C (p.Ala156Pro)
c.553G>C (p.Ala185Pro)
c.571G>C (p.Ala191Pro)
3g.148741501G=CA1409909758AGTR1c.466G= (p.Ala156=)
c.553G= (p.Ala185=)
c.571G= (p.Ala191=)
3g.148741501G>TCA354887647AGTR1c.466G>T (p.Ala156Ser)
c.553G>T (p.Ala185Ser)
c.571G>T (p.Ala191Ser)
 dbSNP gnomAD v2 gnomAD v4
3g.148741502C>ACA354887649AGTR1c.467C>A (p.Ala156Glu)
c.554C>A (p.Ala185Glu)
c.572C>A (p.Ala191Glu)
3g.148741502C=CA1409909761AGTR1c.467C= (p.Ala156=)
c.554C= (p.Ala185=)
c.572C= (p.Ala191=)
3g.148741502C>GCA354887651AGTR1c.467C>G (p.Ala156Gly)
c.554C>G (p.Ala185Gly)
c.572C>G (p.Ala191Gly)
3g.148741502C>TCA354887654AGTR1c.467C>T (p.Ala156Val)
c.554C>T (p.Ala185Val)
c.572C>T (p.Ala191Val)
 dbSNP gnomAD v2 gnomAD v4
3g.148741503A>CCA436389889AGTR1c.468A>C (p.Ala156=)
c.555A>C (p.Ala185=)
c.573A>C (p.Ala191=)
3g.148741503A>GCA436389891AGTR1c.468A>G (p.Ala156=)
c.555A>G (p.Ala185=)
c.573A>G (p.Ala191=)
3g.148741503A>TCA436389895AGTR1c.468A>T (p.Ala156=)
c.555A>T (p.Ala185=)
c.573A>T (p.Ala191=)
3g.148741504G>ACA354887660AGTR1c.469G>A (p.Gly157Ser)
c.556G>A (p.Gly186Ser)
c.574G>A (p.Gly192Ser)
 dbSNP gnomAD v4
3g.148741504G>CCA354887661AGTR1c.469G>C (p.Gly157Arg)
c.556G>C (p.Gly186Arg)
c.574G>C (p.Gly192Arg)
3g.148741504G=CA1409909763AGTR1c.469G= (p.Gly157=)
c.556G= (p.Gly186=)
c.574G= (p.Gly192=)
3g.148741504G>TCA354887664AGTR1c.469G>T (p.Gly157Cys)
c.556G>T (p.Gly186Cys)
c.574G>T (p.Gly192Cys)
3g.148741505G>ACA354887669AGTR1c.470G>A (p.Gly157Asp)
c.557G>A (p.Gly186Asp)
c.575G>A (p.Gly192Asp)
 gnomAD v4
3g.148741505G>CCA85497736AGTR1c.470G>C (p.Gly157Ala)
c.557G>C (p.Gly186Ala)
c.575G>C (p.Gly192Ala)
 dbSNP gnomAD v2 gnomAD v4
3g.148741505G=CA1409909765AGTR1c.470G= (p.Gly157=)
c.557G= (p.Gly186=)
c.575G= (p.Gly192=)
3g.148741505G>TCA354887666AGTR1c.470G>T (p.Gly157Val)
c.557G>T (p.Gly186Val)
c.575G>T (p.Gly192Val)
3g.148741506C>ACA436389901AGTR1c.471C>A (p.Gly157=)
c.558C>A (p.Gly186=)
c.576C>A (p.Gly192=)
 gnomAD v4
3g.148741506C=CA1409909767AGTR1c.471C= (p.Gly157=)
c.558C= (p.Gly186=)
c.576C= (p.Gly192=)
3g.148741506C>GCA436389899AGTR1c.471C>G (p.Gly157=)
c.558C>G (p.Gly186=)
c.576C>G (p.Gly192=)
3g.148741506C>TCA436389900AGTR1c.471C>T (p.Gly157=)
c.558C>T (p.Gly186=)
c.576C>T (p.Gly192=)
 dbSNP gnomAD v4
3g.148741507T>ACA354887672AGTR1c.472T>A (p.Leu158Met)
c.559T>A (p.Leu187Met)
c.577T>A (p.Leu193Met)
3g.148741507T>CCA436389905AGTR1c.472T>C (p.Leu158=)
c.559T>C (p.Leu187=)
c.577T>C (p.Leu193=)
3g.148741507T>GCA354887674AGTR1c.472T>G (p.Leu158Val)
c.559T>G (p.Leu187Val)
c.577T>G (p.Leu193Val)
3g.148741508T>ACA354887677AGTR1c.473T>A (p.Leu158Ter)
c.560T>A (p.Leu187Ter)
c.578T>A (p.Leu193Ter)
3g.148741508T>CCA354887682AGTR1c.473T>C (p.Leu158Ser)
c.560T>C (p.Leu187Ser)
c.578T>C (p.Leu193Ser)
3g.148741508T>GCA354887683AGTR1c.473T>G (p.Leu158Trp)
c.560T>G (p.Leu187Trp)
c.578T>G (p.Leu193Trp)
3g.148741509G>ACA436389433AGTR1c.474G>A (p.Leu158=)
c.561G>A (p.Leu187=)
c.579G>A (p.Leu193=)
3g.148741509G>CCA354887686AGTR1c.474G>C (p.Leu158Phe)
c.561G>C (p.Leu187Phe)
c.579G>C (p.Leu193Phe)
3g.148741509G>TCA354887691AGTR1c.474G>T (p.Leu158Phe)
c.561G>T (p.Leu187Phe)
c.579G>T (p.Leu193Phe)
3g.148741510G>ACA354887692AGTR1c.475G>A (p.Ala159Thr)
c.562G>A (p.Ala188Thr)
c.580G>A (p.Ala194Thr)
3g.148741510G>CCA354887694AGTR1c.475G>C (p.Ala159Pro)
c.562G>C (p.Ala188Pro)
c.580G>C (p.Ala194Pro)
3g.148741510G>TCA354887696AGTR1c.475G>T (p.Ala159Ser)
c.562G>T (p.Ala188Ser)
c.580G>T (p.Ala194Ser)
3g.148741511C>ACA354887698AGTR1c.476C>A (p.Ala159Asp)
c.563C>A (p.Ala188Asp)
c.581C>A (p.Ala194Asp)
3g.148741511C=CA1409909770AGTR1c.476C= (p.Ala159=)
c.563C= (p.Ala188=)
c.581C= (p.Ala194=)
3g.148741511C>GCA354887699AGTR1c.476C>G (p.Ala159Gly)
c.563C>G (p.Ala188Gly)
c.581C>G (p.Ala194Gly)
3g.148741511C>TCA354887704AGTR1c.476C>T (p.Ala159Val)
c.563C>T (p.Ala188Val)
c.581C>T (p.Ala194Val)
 dbSNP COSMIC
3g.148741512C>ACA436389435AGTR1c.477C>A (p.Ala159=)
c.564C>A (p.Ala188=)
c.582C>A (p.Ala194=)
3g.148741512C=CA1409909772AGTR1c.477C= (p.Ala159=)
c.564C= (p.Ala188=)
c.582C= (p.Ala194=)
3g.148741512C>GCA436389434AGTR1c.477C>G (p.Ala159=)
c.564C>G (p.Ala188=)
c.582C>G (p.Ala194=)
3g.148741512C>TCA85497743AGTR1c.477C>T (p.Ala159=)
c.564C>T (p.Ala188=)
c.582C>T (p.Ala194=)
 dbSNP gnomAD v3 gnomAD v4
3g.148741513A>CCA354887715AGTR1c.478A>C (p.Ser160Arg)
c.565A>C (p.Ser189Arg)
c.583A>C (p.Ser195Arg)
3g.148741513A>GCA354887713AGTR1c.478A>G (p.Ser160Gly)
c.565A>G (p.Ser189Gly)
c.583A>G (p.Ser195Gly)
3g.148741513A>TCA354887707AGTR1c.478A>T (p.Ser160Cys)
c.565A>T (p.Ser189Cys)
c.583A>T (p.Ser195Cys)
3g.148741514G>ACA354887719AGTR1c.479G>A (p.Ser160Asn)
c.566G>A (p.Ser189Asn)
c.584G>A (p.Ser195Asn)
3g.148741514G>CCA354887721AGTR1c.479G>C (p.Ser160Thr)
c.566G>C (p.Ser189Thr)
c.584G>C (p.Ser195Thr)
3g.148741514G>TCA354887725AGTR1c.479G>T (p.Ser160Ile)
c.566G>T (p.Ser189Ile)
c.584G>T (p.Ser195Ile)
3g.148741515T>ACA354887728AGTR1c.480T>A (p.Ser160Arg)
c.567T>A (p.Ser189Arg)
c.585T>A (p.Ser195Arg)
3g.148741515T>CCA436389436AGTR1c.480T>C (p.Ser160=)
c.567T>C (p.Ser189=)
c.585T>C (p.Ser195=)
3g.148741515T>GCA354887730AGTR1c.480T>G (p.Ser160Arg)
c.567T>G (p.Ser189Arg)
c.585T>G (p.Ser195Arg)
3g.148741516T>ACA354887732AGTR1c.481T>A (p.Leu161Met)
c.568T>A (p.Leu190Met)
c.586T>A (p.Leu196Met)
3g.148741516T>CCA436389437AGTR1c.481T>C (p.Leu161=)
c.568T>C (p.Leu190=)
c.586T>C (p.Leu196=)
 dbSNP gnomAD v2 gnomAD v4
3g.148741516T>GCA354887733AGTR1c.481T>G (p.Leu161Val)
c.568T>G (p.Leu190Val)
c.586T>G (p.Leu196Val)
3g.148741516T=CA1409909775AGTR1c.481T= (p.Leu161=)
c.568T= (p.Leu190=)
c.586T= (p.Leu196=)
3g.148741517T>ACA354887737AGTR1c.482T>A (p.Leu161Ter)
c.569T>A (p.Leu190Ter)
c.587T>A (p.Leu196Ter)
3g.148741517T>CCA354887739AGTR1c.482T>C (p.Leu161Ser)
c.569T>C (p.Leu190Ser)
c.587T>C (p.Leu196Ser)
 gnomAD v4
3g.148741517T>GCA354887740AGTR1c.482T>G (p.Leu161Trp)
c.569T>G (p.Leu190Trp)
c.587T>G (p.Leu196Trp)
3g.148741518G>ACA436389438AGTR1c.483G>A (p.Leu161=)
c.570G>A (p.Leu190=)
c.588G>A (p.Leu196=)
 dbSNP
3g.148741518G>CCA354887742AGTR1c.483G>C (p.Leu161Phe)
c.570G>C (p.Leu190Phe)
c.588G>C (p.Leu196Phe)
3g.148741518G=CA1409909777AGTR1c.483G= (p.Leu161=)
c.570G= (p.Leu190=)
c.588G= (p.Leu196=)
3g.148741518G>TCA354887743AGTR1c.483G>T (p.Leu161Phe)
c.570G>T (p.Leu190Phe)
c.588G>T (p.Leu196Phe)
3g.148741519C>ACA354887746AGTR1c.484C>A (p.Pro162Thr)
c.571C>A (p.Pro191Thr)
c.589C>A (p.Pro197Thr)
 dbSNP
3g.148741519C=CA1409909780AGTR1c.484C= (p.Pro162=)
c.571C= (p.Pro191=)
c.589C= (p.Pro197=)
3g.148741519C>GCA354887745AGTR1c.484C>G (p.Pro162Ala)
c.571C>G (p.Pro191Ala)
c.589C>G (p.Pro197Ala)
3g.148741519C>TCA354887744AGTR1c.484C>T (p.Pro162Ser)
c.571C>T (p.Pro191Ser)
c.589C>T (p.Pro197Ser)
 dbSNP gnomAD v3 gnomAD v4
3g.148741520C>ACA354887747AGTR1c.485C>A (p.Pro162Gln)
c.572C>A (p.Pro191Gln)
c.590C>A (p.Pro197Gln)
3g.148741520C>GCA354887748AGTR1c.485C>G (p.Pro162Arg)
c.572C>G (p.Pro191Arg)
c.590C>G (p.Pro197Arg)
3g.148741520C>TCA354887749AGTR1c.485C>T (p.Pro162Leu)
c.572C>T (p.Pro191Leu)
c.590C>T (p.Pro197Leu)
3g.148741521A>CCA436389439AGTR1c.486A>C (p.Pro162=)
c.573A>C (p.Pro191=)
c.591A>C (p.Pro197=)
3g.148741521A>GCA436389440AGTR1c.486A>G (p.Pro162=)
c.573A>G (p.Pro191=)
c.591A>G (p.Pro197=)
3g.148741521A>TCA436389441AGTR1c.486A>T (p.Pro162=)
c.573A>T (p.Pro191=)
c.591A>T (p.Pro197=)
3g.148741522G>ACA2657336AGTR1c.487G>A (p.Ala163Thr)
c.574G>A (p.Ala192Thr)
c.592G>A (p.Ala198Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.148741522G>CCA354887751AGTR1c.487G>C (p.Ala163Pro)
c.574G>C (p.Ala192Pro)
c.592G>C (p.Ala198Pro)
3g.148741522G=CA1409909785AGTR1c.487G= (p.Ala163=)
c.574G= (p.Ala192=)
c.592G= (p.Ala198=)
3g.148741522G>TCA354887757AGTR1c.487G>T (p.Ala163Ser)
c.574G>T (p.Ala192Ser)
c.592G>T (p.Ala198Ser)
3g.148741523C>ACA354887759AGTR1c.488C>A (p.Ala163Asp)
c.575C>A (p.Ala192Asp)
c.593C>A (p.Ala198Asp)
3g.148741523C>GCA354887761AGTR1c.488C>G (p.Ala163Gly)
c.575C>G (p.Ala192Gly)
c.593C>G (p.Ala198Gly)
3g.148741523C>TCA354887763AGTR1c.488C>T (p.Ala163Val)
c.575C>T (p.Ala192Val)
c.593C>T (p.Ala198Val)
3g.148741524T>ACA436389442AGTR1c.489T>A (p.Ala163=)
c.576T>A (p.Ala192=)
c.594T>A (p.Ala198=)
3g.148741524T>CCA436389443AGTR1c.489T>C (p.Ala163=)
c.576T>C (p.Ala192=)
c.594T>C (p.Ala198=)
3g.148741524T>GCA436389444AGTR1c.489T>G (p.Ala163=)
c.576T>G (p.Ala192=)
c.594T>G (p.Ala198=)
3g.148741525A=CA1409909789AGTR1c.490A= (p.Ile164=)
c.577A= (p.Ile193=)
c.595A= (p.Ile199=)
3g.148741525A>CCA354887766AGTR1c.490A>C (p.Ile164Leu)
c.577A>C (p.Ile193Leu)
c.595A>C (p.Ile199Leu)
3g.148741525A>GCA354887767AGTR1c.490A>G (p.Ile164Val)
c.577A>G (p.Ile193Val)
c.595A>G (p.Ile199Val)
 dbSNP
3g.148741525A>TCA354887768AGTR1c.490A>T (p.Ile164Leu)
c.577A>T (p.Ile193Leu)
c.595A>T (p.Ile199Leu)
3g.148741526T>ACA354887773AGTR1c.491T>A (p.Ile164Lys)
c.578T>A (p.Ile193Lys)
c.596T>A (p.Ile199Lys)
3g.148741526T>CCA354887770AGTR1c.491T>C (p.Ile164Thr)
c.578T>C (p.Ile193Thr)
c.596T>C (p.Ile199Thr)
3g.148741526T>GCA354887771AGTR1c.491T>G (p.Ile164Arg)
c.578T>G (p.Ile193Arg)
c.596T>G (p.Ile199Arg)
3g.148741527A>CCA436389445AGTR1c.492A>C (p.Ile164=)
c.579A>C (p.Ile193=)
c.597A>C (p.Ile199=)
3g.148741527A>GCA354887774AGTR1c.492A>G (p.Ile164Met)
c.579A>G (p.Ile193Met)
c.597A>G (p.Ile199Met)
3g.148741527A>TCA436389446AGTR1c.492A>T (p.Ile164=)
c.579A>T (p.Ile193=)
c.597A>T (p.Ile199=)
3g.148741528A>CCA354887776AGTR1c.493A>C (p.Ile165Leu)
c.580A>C (p.Ile194Leu)
c.598A>C (p.Ile200Leu)
3g.148741528A>GCA354887778AGTR1c.493A>G (p.Ile165Val)
c.580A>G (p.Ile194Val)
c.598A>G (p.Ile200Val)
3g.148741528A>TCA354887779AGTR1c.493A>T (p.Ile165Phe)
c.580A>T (p.Ile194Phe)
c.598A>T (p.Ile200Phe)
3g.148741529T>ACA354887781AGTR1c.494T>A (p.Ile165Asn)
c.581T>A (p.Ile194Asn)
c.599T>A (p.Ile200Asn)
3g.148741529T>CCA354887783AGTR1c.494T>C (p.Ile165Thr)
c.581T>C (p.Ile194Thr)
c.599T>C (p.Ile200Thr)
 gnomAD v4
3g.148741529T>GCA354887785AGTR1c.494T>G (p.Ile165Ser)
c.581T>G (p.Ile194Ser)
c.599T>G (p.Ile200Ser)
3g.148741530C>ACA436389447AGTR1c.495C>A (p.Ile165=)
c.582C>A (p.Ile194=)
c.600C>A (p.Ile200=)
3g.148741530C>GCA354887786AGTR1c.495C>G (p.Ile165Met)
c.582C>G (p.Ile194Met)
c.600C>G (p.Ile200Met)
 COSMIC
3g.148741530C>TCA436389448AGTR1c.495C>T (p.Ile165=)
c.582C>T (p.Ile194=)
c.600C>T (p.Ile200=)
3g.148741531C>ACA354887787AGTR1c.496C>A (p.His166Asn)
c.583C>A (p.His195Asn)
c.601C>A (p.His201Asn)
3g.148741531C>GCA354887788AGTR1c.496C>G (p.His166Asp)
c.583C>G (p.His195Asp)
c.601C>G (p.His201Asp)
3g.148741531C>TCA354887789AGTR1c.496C>T (p.His166Tyr)
c.583C>T (p.His195Tyr)
c.601C>T (p.His201Tyr)
 COSMIC
3g.148741532A=CA1409909791AGTR1c.497A= (p.His166=)
c.584A= (p.His195=)
c.602A= (p.His201=)
3g.148741532A>CCA354887793AGTR1c.497A>C (p.His166Pro)
c.584A>C (p.His195Pro)
c.602A>C (p.His201Pro)
3g.148741532A>GCA354887792AGTR1c.497A>G (p.His166Arg)
c.584A>G (p.His195Arg)
c.602A>G (p.His201Arg)
 gnomAD v4
3g.148741532A>TCA354887791AGTR1c.497A>T (p.His166Leu)
c.584A>T (p.His195Leu)
c.602A>T (p.His201Leu)
 dbSNP gnomAD v4
3g.148741533T>ACA354887795AGTR1c.498T>A (p.His166Gln)
c.585T>A (p.His195Gln)
c.603T>A (p.His201Gln)
3g.148741533T>CCA436389449AGTR1c.498T>C (p.His166=)
c.585T>C (p.His195=)
c.603T>C (p.His201=)
3g.148741533T>GCA354887797AGTR1c.498T>G (p.His166Gln)
c.585T>G (p.His195Gln)
c.603T>G (p.His201Gln)
3g.148741534C>ACA436389450AGTR1c.499C>A (p.Arg167=)
c.586C>A (p.Arg196=)
c.604C>A (p.Arg202=)
3g.148741534C=CA1409909794AGTR1c.499C= (p.Arg167=)
c.586C= (p.Arg196=)
c.604C= (p.Arg202=)
3g.148741534C>GCA354887798AGTR1c.499C>G (p.Arg167Gly)
c.586C>G (p.Arg196Gly)
c.604C>G (p.Arg202Gly)
3g.148741534C>TCA2657337AGTR1c.499C>T (p.Arg167Ter)
c.586C>T (p.Arg196Ter)
c.604C>T (p.Arg202Ter)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741535G>ACA2657338AGTR1c.500G>A (p.Arg167Gln)
c.587G>A (p.Arg196Gln)
c.605G>A (p.Arg202Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.148741535G>CCA354887801AGTR1c.500G>C (p.Arg167Pro)
c.587G>C (p.Arg196Pro)
c.605G>C (p.Arg202Pro)
3g.148741535G=CA1409909798AGTR1c.500G= (p.Arg167=)
c.587G= (p.Arg196=)
c.605G= (p.Arg202=)
3g.148741535G>TCA354887803AGTR1c.500G>T (p.Arg167Leu)
c.587G>T (p.Arg196Leu)
c.605G>T (p.Arg202Leu)
3g.148741536A>CCA436389451AGTR1c.501A>C (p.Arg167=)
c.588A>C (p.Arg196=)
c.606A>C (p.Arg202=)
3g.148741536A>GCA436389452AGTR1c.501A>G (p.Arg167=)
c.588A>G (p.Arg196=)
c.606A>G (p.Arg202=)
 gnomAD v4
3g.148741536A>TCA436389453AGTR1c.501A>T (p.Arg167=)
c.588A>T (p.Arg196=)
c.606A>T (p.Arg202=)
3g.148741538delCA2668116561AGTR1c.503del (p.Asn168MetfsTer26)
c.590del (p.Asn197MetfsTer26)
c.608del (p.Asn203MetfsTer26)
 gnomAD v4
3g.148741537A>CCA354887805AGTR1c.502A>C (p.Asn168His)
c.589A>C (p.Asn197His)
c.607A>C (p.Asn203His)
3g.148741537A>GCA354887806AGTR1c.502A>G (p.Asn168Asp)
c.589A>G (p.Asn197Asp)
c.607A>G (p.Asn203Asp)
3g.148741537A>TCA354887807AGTR1c.502A>T (p.Asn168Tyr)
c.589A>T (p.Asn197Tyr)
c.607A>T (p.Asn203Tyr)
3g.148741538A=CA1409909805AGTR1c.503A= (p.Asn168=)
c.590A= (p.Asn197=)
c.608A= (p.Asn203=)
3g.148741538A>CCA354887809AGTR1c.503A>C (p.Asn168Thr)
c.590A>C (p.Asn197Thr)
c.608A>C (p.Asn203Thr)
 dbSNP
3g.148741538A>GCA354887811AGTR1c.503A>G (p.Asn168Ser)
c.590A>G (p.Asn197Ser)
c.608A>G (p.Asn203Ser)
3g.148741538A>TCA354887812AGTR1c.503A>T (p.Asn168Ile)
c.590A>T (p.Asn197Ile)
c.608A>T (p.Asn203Ile)
3g.148741539T>ACA354887814AGTR1c.504T>A (p.Asn168Lys)
c.591T>A (p.Asn197Lys)
c.609T>A (p.Asn203Lys)
3g.148741539T>CCA436389454AGTR1c.504T>C (p.Asn168=)
c.591T>C (p.Asn197=)
c.609T>C (p.Asn203=)
3g.148741539T>GCA354887815AGTR1c.504T>G (p.Asn168Lys)
c.591T>G (p.Asn197Lys)
c.609T>G (p.Asn203Lys)
3g.148741540G>ACA354887821AGTR1c.505G>A (p.Val169Ile)
c.592G>A (p.Val198Ile)
c.610G>A (p.Val204Ile)
3g.148741540G>CCA354887819AGTR1c.505G>C (p.Val169Leu)
c.592G>C (p.Val198Leu)
c.610G>C (p.Val204Leu)
3g.148741540G>TCA354887818AGTR1c.505G>T (p.Val169Leu)
c.592G>T (p.Val198Leu)
c.610G>T (p.Val204Leu)
3g.148741541T>ACA354887823AGTR1c.506T>A (p.Val169Glu)
c.593T>A (p.Val198Glu)
c.611T>A (p.Val204Glu)
3g.148741541T>CCA354887825AGTR1c.506T>C (p.Val169Ala)
c.593T>C (p.Val198Ala)
c.611T>C (p.Val204Ala)
 gnomAD v4
3g.148741541T>GCA354887826AGTR1c.506T>G (p.Val169Gly)
c.593T>G (p.Val198Gly)
c.611T>G (p.Val204Gly)
3g.148741542A=CA1409909811AGTR1c.507A= (p.Val169=)
c.594A= (p.Val198=)
c.612A= (p.Val204=)
3g.148741542A>CCA436389455AGTR1c.507A>C (p.Val169=)
c.594A>C (p.Val198=)
c.612A>C (p.Val204=)
3g.148741542A>GCA85497752AGTR1c.507A>G (p.Val169=)
c.594A>G (p.Val198=)
c.612A>G (p.Val204=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.148741542A>TCA436389456AGTR1c.507A>T (p.Val169=)
c.594A>T (p.Val198=)
c.612A>T (p.Val204=)
3g.148741542_148741544delinsATTCA1409909810AGTR1c.507_509delinsATT (p.Val169=)
c.594_596delinsATT (p.Val198=)
c.612_614delinsATT (p.Val204=)
3g.148741543T>ACA354887828AGTR1c.508T>A (p.Phe170Ile)
c.595T>A (p.Phe199Ile)
c.613T>A (p.Phe205Ile)
3g.148741543T>CCA354887830AGTR1c.508T>C (p.Phe170Leu)
c.595T>C (p.Phe199Leu)
c.613T>C (p.Phe205Leu)
3g.148741543T>GCA354887831AGTR1c.508T>G (p.Phe170Val)
c.595T>G (p.Phe199Val)
c.613T>G (p.Phe205Val)
3g.148741546_148741547delCA2657339AGTR1c.511_512del (p.Phe171HisfsTer2)
c.598_599del (p.Phe200HisfsTer2)
c.616_617del (p.Phe206HisfsTer2)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741544T>ACA354887834AGTR1c.509T>A (p.Phe170Tyr)
c.596T>A (p.Phe199Tyr)
c.614T>A (p.Phe205Tyr)
3g.148741544T>CCA354887835AGTR1c.509T>C (p.Phe170Ser)
c.596T>C (p.Phe199Ser)
c.614T>C (p.Phe205Ser)
3g.148741544T>GCA354887837AGTR1c.509T>G (p.Phe170Cys)
c.596T>G (p.Phe199Cys)
c.614T>G (p.Phe205Cys)
3g.148741545T>ACA354887839AGTR1c.510T>A (p.Phe170Leu)
c.597T>A (p.Phe199Leu)
c.615T>A (p.Phe205Leu)
3g.148741545T>CCA436389457AGTR1c.510T>C (p.Phe170=)
c.597T>C (p.Phe199=)
c.615T>C (p.Phe205=)
3g.148741545T>GCA354887841AGTR1c.510T>G (p.Phe170Leu)
c.597T>G (p.Phe199Leu)
c.615T>G (p.Phe205Leu)
3g.148741546T>ACA354887843AGTR1c.511T>A (p.Phe171Ile)
c.598T>A (p.Phe200Ile)
c.616T>A (p.Phe206Ile)
3g.148741546T>CCA354887845AGTR1c.511T>C (p.Phe171Leu)
c.598T>C (p.Phe200Leu)
c.616T>C (p.Phe206Leu)
3g.148741546T>GCA354887842AGTR1c.511T>G (p.Phe171Val)
c.598T>G (p.Phe200Val)
c.616T>G (p.Phe206Val)
3g.148741547T>ACA354887847AGTR1c.512T>A (p.Phe171Tyr)
c.599T>A (p.Phe200Tyr)
c.617T>A (p.Phe206Tyr)
3g.148741547T>CCA354887848AGTR1c.512T>C (p.Phe171Ser)
c.599T>C (p.Phe200Ser)
c.617T>C (p.Phe206Ser)
3g.148741547T>GCA354887850AGTR1c.512T>G (p.Phe171Cys)
c.599T>G (p.Phe200Cys)
c.617T>G (p.Phe206Cys)
3g.148741548C>ACA354887851AGTR1c.513C>A (p.Phe171Leu)
c.600C>A (p.Phe200Leu)
c.618C>A (p.Phe206Leu)
3g.148741548C>GCA354887853AGTR1c.513C>G (p.Phe171Leu)
c.600C>G (p.Phe200Leu)
c.618C>G (p.Phe206Leu)
 COSMIC
3g.148741548C>TCA436389458AGTR1c.513C>T (p.Phe171=)
c.600C>T (p.Phe200=)
c.618C>T (p.Phe206=)
3g.148741549A>CCA354887855AGTR1c.514A>C (p.Ile172Leu)
c.601A>C (p.Ile201Leu)
c.619A>C (p.Ile207Leu)
3g.148741549A>GCA354887857AGTR1c.514A>G (p.Ile172Val)
c.601A>G (p.Ile201Val)
c.619A>G (p.Ile207Val)
3g.148741549A>TCA354887858AGTR1c.514A>T (p.Ile172Phe)
c.601A>T (p.Ile201Phe)
c.619A>T (p.Ile207Phe)
3g.148741550T>ACA354887860AGTR1c.515T>A (p.Ile172Asn)
c.602T>A (p.Ile201Asn)
c.620T>A (p.Ile207Asn)
3g.148741550T>CCA2657340AGTR1c.515T>C (p.Ile172Thr)
c.602T>C (p.Ile201Thr)
c.620T>C (p.Ile207Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741550T>GCA354887863AGTR1c.515T>G (p.Ile172Ser)
c.602T>G (p.Ile201Ser)
c.620T>G (p.Ile207Ser)
3g.148741550T=CA1409909815AGTR1c.515T= (p.Ile172=)
c.602T= (p.Ile201=)
c.620T= (p.Ile207=)
3g.148741551T>ACA436389459AGTR1c.516T>A (p.Ile172=)
c.603T>A (p.Ile201=)
c.621T>A (p.Ile207=)
3g.148741551T>CCA436389460AGTR1c.516T>C (p.Ile172=)
c.603T>C (p.Ile201=)
c.621T>C (p.Ile207=)
3g.148741551T>GCA354887865AGTR1c.516T>G (p.Ile172Met)
c.603T>G (p.Ile201Met)
c.621T>G (p.Ile207Met)
 gnomAD v4
3g.148741552G>ACA354887867AGTR1c.517G>A (p.Glu173Lys)
c.604G>A (p.Glu202Lys)
c.622G>A (p.Glu208Lys)
3g.148741552G>CCA85497764AGTR1c.517G>C (p.Glu173Gln)
c.604G>C (p.Glu202Gln)
c.622G>C (p.Glu208Gln)
 dbSNP gnomAD v4
3g.148741552G=CA1409909817AGTR1c.517G= (p.Glu173=)
c.604G= (p.Glu202=)
c.622G= (p.Glu208=)
3g.148741552G>TCA354887866AGTR1c.517G>T (p.Glu173Ter)
c.604G>T (p.Glu202Ter)
c.622G>T (p.Glu208Ter)

Number of alleles fetched