Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.148741573T>ACA354887927AGTR1c.538T>A (p.Cys180Ser)
c.625T>A (p.Cys209Ser)
c.643T>A (p.Cys215Ser)
3g.148741573T>CCA354887929AGTR1c.538T>C (p.Cys180Arg)
c.625T>C (p.Cys209Arg)
c.643T>C (p.Cys215Arg)
3g.148741573T>GCA354887931AGTR1c.538T>G (p.Cys180Gly)
c.625T>G (p.Cys209Gly)
c.643T>G (p.Cys215Gly)
3g.148741574G>ACA354887939AGTR1c.539G>A (p.Cys180Tyr)
c.626G>A (p.Cys209Tyr)
c.644G>A (p.Cys215Tyr)
3g.148741574G>CCA354887940AGTR1c.539G>C (p.Cys180Ser)
c.626G>C (p.Cys209Ser)
c.644G>C (p.Cys215Ser)
3g.148741574G>TCA354887942AGTR1c.539G>T (p.Cys180Phe)
c.626G>T (p.Cys209Phe)
c.644G>T (p.Cys215Phe)
3g.148741575T>ACA354887945AGTR1c.540T>A (p.Cys180Ter)
c.627T>A (p.Cys209Ter)
c.645T>A (p.Cys215Ter)
3g.148741575T>CCA436389486AGTR1c.540T>C (p.Cys180=)
c.627T>C (p.Cys209=)
c.645T>C (p.Cys215=)
 gnomAD v4
3g.148741575T>GCA354887943AGTR1c.540T>G (p.Cys180Trp)
c.627T>G (p.Cys209Trp)
c.645T>G (p.Cys215Trp)
3g.148741576G>ACA354887946AGTR1c.541G>A (p.Ala181Thr)
c.628G>A (p.Ala210Thr)
c.646G>A (p.Ala216Thr)
3g.148741576G>CCA354887947AGTR1c.541G>C (p.Ala181Pro)
c.628G>C (p.Ala210Pro)
c.646G>C (p.Ala216Pro)
3g.148741576G>TCA354887948AGTR1c.541G>T (p.Ala181Ser)
c.628G>T (p.Ala210Ser)
c.646G>T (p.Ala216Ser)
3g.148741577C>ACA354887951AGTR1c.542C>A (p.Ala181Asp)
c.629C>A (p.Ala210Asp)
c.647C>A (p.Ala216Asp)
 gnomAD v4
3g.148741577C>GCA354887956AGTR1c.542C>G (p.Ala181Gly)
c.629C>G (p.Ala210Gly)
c.647C>G (p.Ala216Gly)
3g.148741577C>TCA354887958AGTR1c.542C>T (p.Ala181Val)
c.629C>T (p.Ala210Val)
c.647C>T (p.Ala216Val)
 COSMIC
3g.148741578T>ACA436389491AGTR1c.543T>A (p.Ala181=)
c.630T>A (p.Ala210=)
c.648T>A (p.Ala216=)
3g.148741578T>CCA436389492AGTR1c.543T>C (p.Ala181=)
c.630T>C (p.Ala210=)
c.648T>C (p.Ala216=)
3g.148741578T>GCA436389493AGTR1c.543T>G (p.Ala181=)
c.630T>G (p.Ala210=)
c.648T>G (p.Ala216=)
3g.148741579T>ACA354887960AGTR1c.544T>A (p.Phe182Ile)
c.631T>A (p.Phe211Ile)
c.649T>A (p.Phe217Ile)
3g.148741579T>CCA354887965AGTR1c.544T>C (p.Phe182Leu)
c.631T>C (p.Phe211Leu)
c.649T>C (p.Phe217Leu)
3g.148741579T>GCA354887962AGTR1c.544T>G (p.Phe182Val)
c.631T>G (p.Phe211Val)
c.649T>G (p.Phe217Val)
3g.148741580T>ACA354887966AGTR1c.545T>A (p.Phe182Tyr)
c.632T>A (p.Phe211Tyr)
c.650T>A (p.Phe217Tyr)
3g.148741580T>CCA354887967AGTR1c.545T>C (p.Phe182Ser)
c.632T>C (p.Phe211Ser)
c.650T>C (p.Phe217Ser)
3g.148741580T>GCA354887968AGTR1c.545T>G (p.Phe182Cys)
c.632T>G (p.Phe211Cys)
c.650T>G (p.Phe217Cys)
3g.148741581C>ACA354887970AGTR1c.546C>A (p.Phe182Leu)
c.633C>A (p.Phe211Leu)
c.651C>A (p.Phe217Leu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.148741581C=CA1409909841AGTR1c.546C= (p.Phe182=)
c.633C= (p.Phe211=)
c.651C= (p.Phe217=)
3g.148741581C>GCA354887973AGTR1c.546C>G (p.Phe182Leu)
c.633C>G (p.Phe211Leu)
c.651C>G (p.Phe217Leu)
3g.148741581C>TCA85497785AGTR1c.546C>T (p.Phe182=)
c.633C>T (p.Phe211=)
c.651C>T (p.Phe217=)
 dbSNP COSMIC
3g.148741582C>ACA354887977AGTR1c.547C>A (p.His183Asn)
c.634C>A (p.His212Asn)
c.652C>A (p.His218Asn)
3g.148741582C>GCA354887979AGTR1c.547C>G (p.His183Asp)
c.634C>G (p.His212Asp)
c.652C>G (p.His218Asp)
3g.148741582C>TCA354887981AGTR1c.547C>T (p.His183Tyr)
c.634C>T (p.His212Tyr)
c.652C>T (p.His218Tyr)
 COSMIC
3g.148741583A=CA1409909845AGTR1c.548A= (p.His183=)
c.635A= (p.His212=)
c.653A= (p.His218=)
3g.148741583A>CCA354887982AGTR1c.548A>C (p.His183Pro)
c.635A>C (p.His212Pro)
c.653A>C (p.His218Pro)
3g.148741583A>GCA354887983AGTR1c.548A>G (p.His183Arg)
c.635A>G (p.His212Arg)
c.653A>G (p.His218Arg)
 dbSNP gnomAD v2 gnomAD v4
3g.148741583A>TCA354887984AGTR1c.548A>T (p.His183Leu)
c.635A>T (p.His212Leu)
c.653A>T (p.His218Leu)
 dbSNP gnomAD v3 gnomAD v4
3g.148741584T>ACA354887986AGTR1c.549T>A (p.His183Gln)
c.636T>A (p.His212Gln)
c.654T>A (p.His218Gln)
3g.148741584T>CCA2657344AGTR1c.549T>C (p.His183=)
c.636T>C (p.His212=)
c.654T>C (p.His218=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741584T>GCA354887985AGTR1c.549T>G (p.His183Gln)
c.636T>G (p.His212Gln)
c.654T>G (p.His218Gln)
3g.148741584T=CA1409909847AGTR1c.549T= (p.His183=)
c.636T= (p.His212=)
c.654T= (p.His218=)
3g.148741585T>ACA354887987AGTR1c.550T>A (p.Tyr184Asn)
c.637T>A (p.Tyr213Asn)
c.655T>A (p.Tyr219Asn)
3g.148741585T>CCA2657345AGTR1c.550T>C (p.Tyr184His)
c.637T>C (p.Tyr213His)
c.655T>C (p.Tyr219His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741585T>GCA354887988AGTR1c.550T>G (p.Tyr184Asp)
c.637T>G (p.Tyr213Asp)
c.655T>G (p.Tyr219Asp)
3g.148741585T=CA1409909850AGTR1c.550T= (p.Tyr184=)
c.637T= (p.Tyr213=)
c.655T= (p.Tyr219=)
3g.148741586A>CCA354887990AGTR1c.551A>C (p.Tyr184Ser)
c.638A>C (p.Tyr213Ser)
c.656A>C (p.Tyr219Ser)
3g.148741586A>GCA354887992AGTR1c.551A>G (p.Tyr184Cys)
c.638A>G (p.Tyr213Cys)
c.656A>G (p.Tyr219Cys)
 gnomAD v4
3g.148741586A>TCA354887993AGTR1c.551A>T (p.Tyr184Phe)
c.638A>T (p.Tyr213Phe)
c.656A>T (p.Tyr219Phe)
3g.148741587T>ACA354887994AGTR1c.552T>A (p.Tyr184Ter)
c.639T>A (p.Tyr213Ter)
c.657T>A (p.Tyr219Ter)
3g.148741587T>CCA436389500AGTR1c.552T>C (p.Tyr184=)
c.639T>C (p.Tyr213=)
c.657T>C (p.Tyr219=)
 COSMIC
3g.148741587T>GCA354887995AGTR1c.552T>G (p.Tyr184Ter)
c.639T>G (p.Tyr213Ter)
c.657T>G (p.Tyr219Ter)
3g.148741588G>ACA2657346AGTR1c.553G>A (p.Glu185Lys)
c.640G>A (p.Glu214Lys)
c.658G>A (p.Glu220Lys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741588G>CCA354887997AGTR1c.553G>C (p.Glu185Gln)
c.640G>C (p.Glu214Gln)
c.658G>C (p.Glu220Gln)
3g.148741588G=CA1409909851AGTR1c.553G= (p.Glu185=)
c.640G= (p.Glu214=)
c.658G= (p.Glu220=)
3g.148741588G>TCA354887999AGTR1c.553G>T (p.Glu185Ter)
c.640G>T (p.Glu214Ter)
c.658G>T (p.Glu220Ter)
3g.148741589A>CCA354888003AGTR1c.554A>C (p.Glu185Ala)
c.641A>C (p.Glu214Ala)
c.659A>C (p.Glu220Ala)
3g.148741589A>GCA354888004AGTR1c.554A>G (p.Glu185Gly)
c.641A>G (p.Glu214Gly)
c.659A>G (p.Glu220Gly)
3g.148741589A>TCA354888007AGTR1c.554A>T (p.Glu185Val)
c.641A>T (p.Glu214Val)
c.659A>T (p.Glu220Val)
3g.148741590G>ACA436389501AGTR1c.555G>A (p.Glu185=)
c.642G>A (p.Glu214=)
c.660G>A (p.Glu220=)
 dbSNP gnomAD v4
3g.148741590G>CCA354888010AGTR1c.555G>C (p.Glu185Asp)
c.642G>C (p.Glu214Asp)
c.660G>C (p.Glu220Asp)
 gnomAD v4
3g.148741590G=CA1409909854AGTR1c.555G= (p.Glu185=)
c.642G= (p.Glu214=)
c.660G= (p.Glu220=)
3g.148741590G>TCA354888012AGTR1c.555G>T (p.Glu185Asp)
c.642G>T (p.Glu214Asp)
c.660G>T (p.Glu220Asp)
3g.148741591T>ACA354888019AGTR1c.556T>A (p.Ser186Thr)
c.643T>A (p.Ser215Thr)
c.661T>A (p.Ser221Thr)
3g.148741591T>CCA2657347AGTR1c.556T>C (p.Ser186Pro)
c.643T>C (p.Ser215Pro)
c.661T>C (p.Ser221Pro)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741591T>GCA354888015AGTR1c.556T>G (p.Ser186Ala)
c.643T>G (p.Ser215Ala)
c.661T>G (p.Ser221Ala)
3g.148741591T=CA1409909858AGTR1c.556T= (p.Ser186=)
c.643T= (p.Ser215=)
c.661T= (p.Ser221=)
3g.148741592C>ACA354888021AGTR1c.557C>A (p.Ser186Tyr)
c.644C>A (p.Ser215Tyr)
c.662C>A (p.Ser221Tyr)
3g.148741592C=CA1409909860AGTR1c.557C= (p.Ser186=)
c.644C= (p.Ser215=)
c.662C= (p.Ser221=)
3g.148741592C>GCA354888024AGTR1c.557C>G (p.Ser186Cys)
c.644C>G (p.Ser215Cys)
c.662C>G (p.Ser221Cys)
3g.148741592C>TCA354888033AGTR1c.557C>T (p.Ser186Phe)
c.644C>T (p.Ser215Phe)
c.662C>T (p.Ser221Phe)
 dbSNP gnomAD v2 gnomAD v4
3g.148741593C>ACA436389505AGTR1c.558C>A (p.Ser186=)
c.645C>A (p.Ser215=)
c.663C>A (p.Ser221=)
3g.148741593C>GCA436389507AGTR1c.558C>G (p.Ser186=)
c.645C>G (p.Ser215=)
c.663C>G (p.Ser221=)
3g.148741593C>TCA436389506AGTR1c.558C>T (p.Ser186=)
c.645C>T (p.Ser215=)
c.663C>T (p.Ser221=)
3g.148741594C>ACA354888038AGTR1c.559C>A (p.Gln187Lys)
c.646C>A (p.Gln216Lys)
c.664C>A (p.Gln222Lys)
3g.148741594C>GCA354888039AGTR1c.559C>G (p.Gln187Glu)
c.646C>G (p.Gln216Glu)
c.664C>G (p.Gln222Glu)
3g.148741594C>TCA354888041AGTR1c.559C>T (p.Gln187Ter)
c.646C>T (p.Gln216Ter)
c.664C>T (p.Gln222Ter)
3g.148741595A>CCA354888044AGTR1c.560A>C (p.Gln187Pro)
c.647A>C (p.Gln216Pro)
c.665A>C (p.Gln222Pro)
3g.148741595A>GCA354888049AGTR1c.560A>G (p.Gln187Arg)
c.647A>G (p.Gln216Arg)
c.665A>G (p.Gln222Arg)
3g.148741595A>TCA354888052AGTR1c.560A>T (p.Gln187Leu)
c.647A>T (p.Gln216Leu)
c.665A>T (p.Gln222Leu)
3g.148741596A>CCA354888055AGTR1c.561A>C (p.Gln187His)
c.648A>C (p.Gln216His)
c.666A>C (p.Gln222His)
3g.148741596A>GCA436389511AGTR1c.561A>G (p.Gln187=)
c.648A>G (p.Gln216=)
c.666A>G (p.Gln222=)
3g.148741596A>TCA354888056AGTR1c.561A>T (p.Gln187His)
c.648A>T (p.Gln216His)
c.666A>T (p.Gln222His)
3g.148741597A=CA1409909867AGTR1c.562A= (p.Asn188=)
c.649A= (p.Asn217=)
c.667A= (p.Asn223=)
3g.148741597A>CCA354888059AGTR1c.562A>C (p.Asn188His)
c.649A>C (p.Asn217His)
c.667A>C (p.Asn223His)
3g.148741597A>GCA85497826AGTR1c.562A>G (p.Asn188Asp)
c.649A>G (p.Asn217Asp)
c.667A>G (p.Asn223Asp)
 dbSNP gnomAD v2 gnomAD v4
3g.148741597A>TCA2657348AGTR1c.562A>T (p.Asn188Tyr)
c.649A>T (p.Asn217Tyr)
c.667A>T (p.Asn223Tyr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741597_148741598insCACACCCAACACCA2758831858AGTR1c.562_563insCACACCCAACAC (p.Asn188delinsThrHisProThrHis)
c.649_650insCACACCCAACAC (p.Asn217delinsThrHisProThrHis)
c.667_668insCACACCCAACAC (p.Asn223delinsThrHisProThrHis)
3g.148741598A>CCA354888064AGTR1c.563A>C (p.Asn188Thr)
c.650A>C (p.Asn217Thr)
c.668A>C (p.Asn223Thr)
3g.148741598A>GCA354888062AGTR1c.563A>G (p.Asn188Ser)
c.650A>G (p.Asn217Ser)
c.668A>G (p.Asn223Ser)
3g.148741598A>TCA354888061AGTR1c.563A>T (p.Asn188Ile)
c.650A>T (p.Asn217Ile)
c.668A>T (p.Asn223Ile)
3g.148741598_148741599insAAACCCAAACACACCCAACACACA2758831857AGTR1c.563_564insAAACCCAAACACACCCAACACA (p.Asn188LysfsTer?)
c.650_651insAAACCCAAACACACCCAACACA (p.Asn217LysfsTer?)
c.668_669insAAACCCAAACACACCCAACACA (p.Asn223LysfsTer?)
3g.148741599T>ACA354888068AGTR1c.564T>A (p.Asn188Lys)
c.651T>A (p.Asn217Lys)
c.669T>A (p.Asn223Lys)
3g.148741599T>CCA436389513AGTR1c.564T>C (p.Asn188=)
c.651T>C (p.Asn217=)
c.669T>C (p.Asn223=)
3g.148741599T>GCA354888071AGTR1c.564T>G (p.Asn188Lys)
c.651T>G (p.Asn217Lys)
c.669T>G (p.Asn223Lys)
 dbSNP
3g.148741600T>ACA354888073AGTR1c.565T>A (p.Ser189Thr)
c.652T>A (p.Ser218Thr)
c.670T>A (p.Ser224Thr)
3g.148741600T>CCA85497842AGTR1c.565T>C (p.Ser189Pro)
c.652T>C (p.Ser218Pro)
c.670T>C (p.Ser224Pro)
 dbSNP
3g.148741600T>GCA354888076AGTR1c.565T>G (p.Ser189Ala)
c.652T>G (p.Ser218Ala)
c.670T>G (p.Ser224Ala)
3g.148741600T=CA1409909871AGTR1c.565T= (p.Ser189=)
c.652T= (p.Ser218=)
c.670T= (p.Ser224=)
3g.148741601C>ACA354888085AGTR1c.566C>A (p.Ser189Ter)
c.653C>A (p.Ser218Ter)
c.671C>A (p.Ser224Ter)
3g.148741601C=CA1409909873AGTR1c.566C= (p.Ser189=)
c.653C= (p.Ser218=)
c.671C= (p.Ser224=)
3g.148741601C>GCA354888083AGTR1c.566C>G (p.Ser189Ter)
c.653C>G (p.Ser218Ter)
c.671C>G (p.Ser224Ter)
3g.148741601C>TCA2657349AGTR1c.566C>T (p.Ser189Leu)
c.653C>T (p.Ser218Leu)
c.671C>T (p.Ser224Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741602A=CA1409909876AGTR1c.567A= (p.Ser189=)
c.654A= (p.Ser218=)
c.672A= (p.Ser224=)
3g.148741602A>CCA436389519AGTR1c.567A>C (p.Ser189=)
c.654A>C (p.Ser218=)
c.672A>C (p.Ser224=)
3g.148741602A>GCA436389517AGTR1c.567A>G (p.Ser189=)
c.654A>G (p.Ser218=)
c.672A>G (p.Ser224=)
 dbSNP gnomAD v4 COSMIC
3g.148741602A>TCA436389518AGTR1c.567A>T (p.Ser189=)
c.654A>T (p.Ser218=)
c.672A>T (p.Ser224=)
3g.148741603A=CA1409909879AGTR1c.568A= (p.Thr190=)
c.655A= (p.Thr219=)
c.673A= (p.Thr225=)
3g.148741603A>CCA354888086AGTR1c.568A>C (p.Thr190Pro)
c.655A>C (p.Thr219Pro)
c.673A>C (p.Thr225Pro)
 dbSNP
3g.148741603A>GCA354888087AGTR1c.568A>G (p.Thr190Ala)
c.655A>G (p.Thr219Ala)
c.673A>G (p.Thr225Ala)
3g.148741603A>TCA354888088AGTR1c.568A>T (p.Thr190Ser)
c.655A>T (p.Thr219Ser)
c.673A>T (p.Thr225Ser)
3g.148741604C>ACA354888090AGTR1c.569C>A (p.Thr190Asn)
c.656C>A (p.Thr219Asn)
c.674C>A (p.Thr225Asn)
 COSMIC
3g.148741604C=CA1409909881AGTR1c.569C= (p.Thr190=)
c.656C= (p.Thr219=)
c.674C= (p.Thr225=)
3g.148741604C>GCA85497856AGTR1c.569C>G (p.Thr190Ser)
c.656C>G (p.Thr219Ser)
c.674C>G (p.Thr225Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.148741604C>TCA354888095AGTR1c.569C>T (p.Thr190Ile)
c.656C>T (p.Thr219Ile)
c.674C>T (p.Thr225Ile)
3g.148741605C>ACA436389523AGTR1c.570C>A (p.Thr190=)
c.657C>A (p.Thr219=)
c.675C>A (p.Thr225=)
3g.148741605C=CA1409909884AGTR1c.570C= (p.Thr190=)
c.657C= (p.Thr219=)
c.675C= (p.Thr225=)
3g.148741605C>GCA436389524AGTR1c.570C>G (p.Thr190=)
c.657C>G (p.Thr219=)
c.675C>G (p.Thr225=)
 gnomAD v4
3g.148741605C>TCA85497866AGTR1c.570C>T (p.Thr190=)
c.657C>T (p.Thr219=)
c.675C>T (p.Thr225=)
 dbSNP gnomAD v4 COSMIC
3g.148741606C>ACA354888096AGTR1c.571C>A (p.Leu191Ile)
c.658C>A (p.Leu220Ile)
c.676C>A (p.Leu226Ile)
3g.148741606C=CA1409909891AGTR1c.571C= (p.Leu191=)
c.658C= (p.Leu220=)
c.676C= (p.Leu226=)
3g.148741606C>GCA354888099AGTR1c.571C>G (p.Leu191Val)
c.658C>G (p.Leu220Val)
c.676C>G (p.Leu226Val)
3g.148741606C>TCA2657350AGTR1c.571C>T (p.Leu191Phe)
c.658C>T (p.Leu220Phe)
c.676C>T (p.Leu226Phe)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741607T>ACA354888101AGTR1c.572T>A (p.Leu191His)
c.659T>A (p.Leu220His)
c.677T>A (p.Leu226His)
3g.148741607T>CCA354888105AGTR1c.572T>C (p.Leu191Pro)
c.659T>C (p.Leu220Pro)
c.677T>C (p.Leu226Pro)
3g.148741607T>GCA354888107AGTR1c.572T>G (p.Leu191Arg)
c.659T>G (p.Leu220Arg)
c.677T>G (p.Leu226Arg)
3g.148741608C>ACA436389525AGTR1c.573C>A (p.Leu191=)
c.660C>A (p.Leu220=)
c.678C>A (p.Leu226=)
3g.148741608C=CA1409909896AGTR1c.573C= (p.Leu191=)
c.660C= (p.Leu220=)
c.678C= (p.Leu226=)
3g.148741608C>GCA436389526AGTR1c.573C>G (p.Leu191=)
c.660C>G (p.Leu220=)
c.678C>G (p.Leu226=)
 dbSNP
3g.148741608C>TCA2657351AGTR1c.573C>T (p.Leu191=)
c.660C>T (p.Leu220=)
c.678C>T (p.Leu226=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741609C>ACA354888110AGTR1c.574C>A (p.Pro192Thr)
c.661C>A (p.Pro221Thr)
c.679C>A (p.Pro227Thr)
3g.148741609C=CA1409909903AGTR1c.574C= (p.Pro192=)
c.661C= (p.Pro221=)
c.679C= (p.Pro227=)
3g.148741609C>GCA354888111AGTR1c.574C>G (p.Pro192Ala)
c.661C>G (p.Pro221Ala)
c.679C>G (p.Pro227Ala)
3g.148741609C>TCA354888115AGTR1c.574C>T (p.Pro192Ser)
c.661C>T (p.Pro221Ser)
c.679C>T (p.Pro227Ser)
 dbSNP gnomAD v2 COSMIC
3g.148741610C>ACA354888117AGTR1c.575C>A (p.Pro192Gln)
c.662C>A (p.Pro221Gln)
c.680C>A (p.Pro227Gln)
 COSMIC
3g.148741610C=CA1409909908AGTR1c.575C= (p.Pro192=)
c.662C= (p.Pro221=)
c.680C= (p.Pro227=)
3g.148741610C>GCA354888121AGTR1c.575C>G (p.Pro192Arg)
c.662C>G (p.Pro221Arg)
c.680C>G (p.Pro227Arg)
3g.148741610C>TCA2657352AGTR1c.575C>T (p.Pro192Leu)
c.662C>T (p.Pro221Leu)
c.680C>T (p.Pro227Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741611G>ACA2657353AGTR1c.576G>A (p.Pro192=)
c.663G>A (p.Pro221=)
c.681G>A (p.Pro227=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.148741611G>CCA436389530AGTR1c.576G>C (p.Pro192=)
c.663G>C (p.Pro221=)
c.681G>C (p.Pro227=)
3g.148741611G=CA1409909911AGTR1c.576G= (p.Pro192=)
c.663G= (p.Pro221=)
c.681G= (p.Pro227=)
3g.148741611G>TCA436389531AGTR1c.576G>T (p.Pro192=)
c.663G>T (p.Pro221=)
c.681G>T (p.Pro227=)
 gnomAD v4
3g.148741612A=CA1409909916AGTR1c.577A= (p.Ile193=)
c.664A= (p.Ile222=)
c.682A= (p.Ile228=)
3g.148741612A>CCA354888128AGTR1c.577A>C (p.Ile193Leu)
c.664A>C (p.Ile222Leu)
c.682A>C (p.Ile228Leu)
 dbSNP gnomAD v2 gnomAD v4
3g.148741612A>GCA354888132AGTR1c.577A>G (p.Ile193Val)
c.664A>G (p.Ile222Val)
c.682A>G (p.Ile228Val)
 gnomAD v4
3g.148741612A>TCA354888131AGTR1c.577A>T (p.Ile193Leu)
c.664A>T (p.Ile222Leu)
c.682A>T (p.Ile228Leu)
3g.148741613T>ACA354888135AGTR1c.578T>A (p.Ile193Lys)
c.665T>A (p.Ile222Lys)
c.683T>A (p.Ile228Lys)
3g.148741613T>CCA354888137AGTR1c.578T>C (p.Ile193Thr)
c.665T>C (p.Ile222Thr)
c.683T>C (p.Ile228Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.148741613T>GCA354888140AGTR1c.578T>G (p.Ile193Arg)
c.665T>G (p.Ile222Arg)
c.683T>G (p.Ile228Arg)
3g.148741613T=CA1409909919AGTR1c.578T= (p.Ile193=)
c.665T= (p.Ile222=)
c.683T= (p.Ile228=)
3g.148741613_148741614insCCA2668116563AGTR1c.578_579insC (p.Gly194ArgfsTer?)
c.665_666insC (p.Gly223ArgfsTer?)
c.683_684insC (p.Gly229ArgfsTer?)
 gnomAD v4
3g.148741614A>CCA436389532AGTR1c.579A>C (p.Ile193=)
c.666A>C (p.Ile222=)
c.684A>C (p.Ile228=)
3g.148741614A>GCA354888143AGTR1c.579A>G (p.Ile193Met)
c.666A>G (p.Ile222Met)
c.684A>G (p.Ile228Met)
3g.148741614A>TCA436389535AGTR1c.579A>T (p.Ile193=)
c.666A>T (p.Ile222=)
c.684A>T (p.Ile228=)
3g.148741615G>ACA354888145AGTR1c.580G>A (p.Gly194Arg)
c.667G>A (p.Gly223Arg)
c.685G>A (p.Gly229Arg)
 dbSNP gnomAD v4 COSMIC
3g.148741615G>CCA354888147AGTR1c.580G>C (p.Gly194Arg)
c.667G>C (p.Gly223Arg)
c.685G>C (p.Gly229Arg)
3g.148741615G>TCA354888149AGTR1c.580G>T (p.Gly194Trp)
c.667G>T (p.Gly223Trp)
c.685G>T (p.Gly229Trp)
3g.148741616G>ACA354888151AGTR1c.581G>A (p.Gly194Glu)
c.668G>A (p.Gly223Glu)
c.686G>A (p.Gly229Glu)
3g.148741616G>CCA85497882AGTR1c.581G>C (p.Gly194Ala)
c.668G>C (p.Gly223Ala)
c.686G>C (p.Gly229Ala)
 dbSNP
3g.148741616G=CA1409909922AGTR1c.581G= (p.Gly194=)
c.668G= (p.Gly223=)
c.686G= (p.Gly229=)
3g.148741616G>TCA354888153AGTR1c.581G>T (p.Gly194Val)
c.668G>T (p.Gly223Val)
c.686G>T (p.Gly229Val)
3g.148741617G>ACA436389537AGTR1c.582G>A (p.Gly194=)
c.669G>A (p.Gly223=)
c.687G>A (p.Gly229=)
 gnomAD v4
3g.148741617G>CCA436389538AGTR1c.582G>C (p.Gly194=)
c.669G>C (p.Gly223=)
c.687G>C (p.Gly229=)
3g.148741617G=CA1409909924AGTR1c.582G= (p.Gly194=)
c.669G= (p.Gly223=)
c.687G= (p.Gly229=)
3g.148741617G>TCA2657354AGTR1c.582G>T (p.Gly194=)
c.669G>T (p.Gly223=)
c.687G>T (p.Gly229=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741618C>ACA354888157AGTR1c.583C>A (p.Leu195Met)
c.670C>A (p.Leu224Met)
c.688C>A (p.Leu230Met)
3g.148741618C>GCA354888160AGTR1c.583C>G (p.Leu195Val)
c.670C>G (p.Leu224Val)
c.688C>G (p.Leu230Val)
3g.148741618C>TCA436389539AGTR1c.583C>T (p.Leu195=)
c.670C>T (p.Leu224=)
c.688C>T (p.Leu230=)
3g.148741618dupCA2577930437AGTR1c.583dup (p.Leu195ProfsTer?)
c.670dup (p.Leu224ProfsTer?)
c.688dup (p.Leu230ProfsTer?)
3g.148741619T>ACA354888163AGTR1c.584T>A (p.Leu195Gln)
c.671T>A (p.Leu224Gln)
c.689T>A (p.Leu230Gln)
3g.148741619T>CCA354888162AGTR1c.584T>C (p.Leu195Pro)
c.671T>C (p.Leu224Pro)
c.689T>C (p.Leu230Pro)
 ClinVar gnomAD v4
3g.148741619T>GCA354888161AGTR1c.584T>G (p.Leu195Arg)
c.671T>G (p.Leu224Arg)
c.689T>G (p.Leu230Arg)
3g.148741620G>ACA436389541AGTR1c.585G>A (p.Leu195=)
c.672G>A (p.Leu224=)
c.690G>A (p.Leu230=)
 dbSNP gnomAD v2
3g.148741620G>CCA436389542AGTR1c.585G>C (p.Leu195=)
c.672G>C (p.Leu224=)
c.690G>C (p.Leu230=)
3g.148741620G=CA1409909927AGTR1c.585G= (p.Leu195=)
c.672G= (p.Leu224=)
c.690G= (p.Leu230=)
3g.148741620G>TCA436389543AGTR1c.585G>T (p.Leu195=)
c.672G>T (p.Leu224=)
c.690G>T (p.Leu230=)
3g.148741621G>ACA354888164AGTR1c.586G>A (p.Gly196Ser)
c.673G>A (p.Gly225Ser)
c.691G>A (p.Gly231Ser)
3g.148741621G>CCA354888165AGTR1c.586G>C (p.Gly196Arg)
c.673G>C (p.Gly225Arg)
c.691G>C (p.Gly231Arg)
3g.148741621G>TCA354888166AGTR1c.586G>T (p.Gly196Cys)
c.673G>T (p.Gly225Cys)
c.691G>T (p.Gly231Cys)
 COSMIC
3g.148741622G>ACA354888167AGTR1c.587G>A (p.Gly196Asp)
c.674G>A (p.Gly225Asp)
c.692G>A (p.Gly231Asp)
3g.148741622G>CCA354888168AGTR1c.587G>C (p.Gly196Ala)
c.674G>C (p.Gly225Ala)
c.692G>C (p.Gly231Ala)
3g.148741622G=CA1409909929AGTR1c.587G= (p.Gly196=)
c.674G= (p.Gly225=)
c.692G= (p.Gly231=)
3g.148741622G>TCA354888169AGTR1c.587G>T (p.Gly196Val)
c.674G>T (p.Gly225Val)
c.692G>T (p.Gly231Val)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
3g.148741623C>ACA436389547AGTR1c.588C>A (p.Gly196=)
c.675C>A (p.Gly225=)
c.693C>A (p.Gly231=)
3g.148741623C=CA1409909931AGTR1c.588C= (p.Gly196=)
c.675C= (p.Gly225=)
c.693C= (p.Gly231=)
3g.148741623C>GCA436389544AGTR1c.588C>G (p.Gly196=)
c.675C>G (p.Gly225=)
c.693C>G (p.Gly231=)
3g.148741623C>TCA436389546AGTR1c.588C>T (p.Gly196=)
c.675C>T (p.Gly225=)
c.693C>T (p.Gly231=)
 dbSNP gnomAD v2 gnomAD v4
3g.148741624C>ACA354888170AGTR1c.589C>A (p.Leu197Met)
c.676C>A (p.Leu226Met)
c.694C>A (p.Leu232Met)
3g.148741624C=CA1409909933AGTR1c.589C= (p.Leu197=)
c.676C= (p.Leu226=)
c.694C= (p.Leu232=)
3g.148741624C>GCA354888171AGTR1c.589C>G (p.Leu197Val)
c.676C>G (p.Leu226Val)
c.694C>G (p.Leu232Val)
3g.148741624C>TCA2657355AGTR1c.589C>T (p.Leu197=)
c.676C>T (p.Leu226=)
c.694C>T (p.Leu232=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741625T>ACA2657356AGTR1c.590T>A (p.Leu197Gln)
c.677T>A (p.Leu226Gln)
c.695T>A (p.Leu232Gln)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741625T>CCA354888172AGTR1c.590T>C (p.Leu197Pro)
c.677T>C (p.Leu226Pro)
c.695T>C (p.Leu232Pro)
3g.148741625T>GCA354888173AGTR1c.590T>G (p.Leu197Arg)
c.677T>G (p.Leu226Arg)
c.695T>G (p.Leu232Arg)
 COSMIC
3g.148741625T=CA1409909937AGTR1c.590T= (p.Leu197=)
c.677T= (p.Leu226=)
c.695T= (p.Leu232=)
3g.148741626G>ACA2657357AGTR1c.591G>A (p.Leu197=)
c.678G>A (p.Leu226=)
c.696G>A (p.Leu232=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741626G>CCA436389550AGTR1c.591G>C (p.Leu197=)
c.678G>C (p.Leu226=)
c.696G>C (p.Leu232=)
 dbSNP gnomAD v3 gnomAD v4
3g.148741626G=CA1409909941AGTR1c.591G= (p.Leu197=)
c.678G= (p.Leu226=)
c.696G= (p.Leu232=)
3g.148741626G>TCA436389552AGTR1c.591G>T (p.Leu197=)
c.678G>T (p.Leu226=)
c.696G>T (p.Leu232=)
 COSMIC
3g.148741627A=CA1409909945AGTR1c.592A= (p.Thr198=)
c.679A= (p.Thr227=)
c.697A= (p.Thr233=)
3g.148741627A>CCA354888181AGTR1c.592A>C (p.Thr198Pro)
c.679A>C (p.Thr227Pro)
c.697A>C (p.Thr233Pro)
3g.148741627A>GCA354888184AGTR1c.592A>G (p.Thr198Ala)
c.679A>G (p.Thr227Ala)
c.697A>G (p.Thr233Ala)
 dbSNP gnomAD v3 gnomAD v4
3g.148741627A>TCA354888180AGTR1c.592A>T (p.Thr198Ser)
c.679A>T (p.Thr227Ser)
c.697A>T (p.Thr233Ser)
3g.148741628C>ACA354888186AGTR1c.593C>A (p.Thr198Asn)
c.680C>A (p.Thr227Asn)
c.698C>A (p.Thr233Asn)
 dbSNP
3g.148741628C=CA1409909949AGTR1c.593C= (p.Thr198=)
c.680C= (p.Thr227=)
c.698C= (p.Thr233=)
3g.148741628C>GCA354888188AGTR1c.593C>G (p.Thr198Ser)
c.680C>G (p.Thr227Ser)
c.698C>G (p.Thr233Ser)
3g.148741628C>TCA354888190AGTR1c.593C>T (p.Thr198Ile)
c.680C>T (p.Thr227Ile)
c.698C>T (p.Thr233Ile)
3g.148741629C>ACA436389555AGTR1c.594C>A (p.Thr198=)
c.681C>A (p.Thr227=)
c.699C>A (p.Thr233=)
 dbSNP gnomAD v2 gnomAD v4
3g.148741629C=CA1409909952AGTR1c.594C= (p.Thr198=)
c.681C= (p.Thr227=)
c.699C= (p.Thr233=)
3g.148741629C>GCA436389559AGTR1c.594C>G (p.Thr198=)
c.681C>G (p.Thr227=)
c.699C>G (p.Thr233=)
3g.148741629C>TCA436389557AGTR1c.594C>T (p.Thr198=)
c.681C>T (p.Thr227=)
c.699C>T (p.Thr233=)
3g.148741630A>CCA354888192AGTR1c.595A>C (p.Lys199Gln)
c.682A>C (p.Lys228Gln)
c.700A>C (p.Lys234Gln)
3g.148741630A>GCA354888194AGTR1c.595A>G (p.Lys199Glu)
c.682A>G (p.Lys228Glu)
c.700A>G (p.Lys234Glu)
3g.148741630A>TCA354888197AGTR1c.595A>T (p.Lys199Ter)
c.682A>T (p.Lys228Ter)
c.700A>T (p.Lys234Ter)
3g.148741634_148741635insAAAAAAAAAAAACA2758831861AGTR1c.599_600insAAAAAAAAAAAA (p.Lys199_Asn200insLysLysLysLys)
c.686_687insAAAAAAAAAAAA (p.Lys228_Asn229insLysLysLysLys)
c.704_705insAAAAAAAAAAAA (p.Lys234_Asn235insLysLysLysLys)
3g.148741634dupCA547365418AGTR1c.599dup (p.Asn200LysfsTer28)
c.686dup (p.Asn229LysfsTer28)
c.704dup (p.Asn235LysfsTer28)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.148741634delCA436389560AGTR1c.599del (p.Asn200IlefsTer10)
c.686del (p.Asn229IlefsTer10)
c.704del (p.Asn235IlefsTer10)
 COSMIC
3g.148741631A>CCA354888199AGTR1c.596A>C (p.Lys199Thr)
c.683A>C (p.Lys228Thr)
c.701A>C (p.Lys234Thr)
3g.148741631A>GCA354888201AGTR1c.596A>G (p.Lys199Arg)
c.683A>G (p.Lys228Arg)
c.701A>G (p.Lys234Arg)
 gnomAD v4
3g.148741631A>TCA354888202AGTR1c.596A>T (p.Lys199Ile)
c.683A>T (p.Lys228Ile)
c.701A>T (p.Lys234Ile)
3g.148741632A>CCA354888205AGTR1c.597A>C (p.Lys199Asn)
c.684A>C (p.Lys228Asn)
c.702A>C (p.Lys234Asn)
3g.148741632A>GCA436389571AGTR1c.597A>G (p.Lys199=)
c.684A>G (p.Lys228=)
c.702A>G (p.Lys234=)
 gnomAD v4
3g.148741632A>TCA354888207AGTR1c.597A>T (p.Lys199Asn)
c.684A>T (p.Lys228Asn)
c.702A>T (p.Lys234Asn)
3g.148741633A>CCA354888212AGTR1c.598A>C (p.Asn200His)
c.685A>C (p.Asn229His)
c.703A>C (p.Asn235His)
 COSMIC
3g.148741633A>GCA354888210AGTR1c.598A>G (p.Asn200Asp)
c.685A>G (p.Asn229Asp)
c.703A>G (p.Asn235Asp)
3g.148741633A>TCA354888208AGTR1c.598A>T (p.Asn200Tyr)
c.685A>T (p.Asn229Tyr)
c.703A>T (p.Asn235Tyr)
3g.148741634A>CCA354888215AGTR1c.599A>C (p.Asn200Thr)
c.686A>C (p.Asn229Thr)
c.704A>C (p.Asn235Thr)
3g.148741634A>GCA354888217AGTR1c.599A>G (p.Asn200Ser)
c.686A>G (p.Asn229Ser)
c.704A>G (p.Asn235Ser)
3g.148741634A>TCA354888218AGTR1c.599A>T (p.Asn200Ile)
c.686A>T (p.Asn229Ile)
c.704A>T (p.Asn235Ile)
3g.148741635T>ACA354888221AGTR1c.600T>A (p.Asn200Lys)
c.687T>A (p.Asn229Lys)
c.705T>A (p.Asn235Lys)
3g.148741635T>CCA436389575AGTR1c.600T>C (p.Asn200=)
c.687T>C (p.Asn229=)
c.705T>C (p.Asn235=)
 gnomAD v4
3g.148741635T>GCA354888223AGTR1c.600T>G (p.Asn200Lys)
c.687T>G (p.Asn229Lys)
c.705T>G (p.Asn235Lys)
 gnomAD v4
3g.148741636A=CA1409909959AGTR1c.601A= (p.Ile201=)
c.688A= (p.Ile230=)
c.706A= (p.Ile236=)
3g.148741636A>CCA354888225AGTR1c.601A>C (p.Ile201Leu)
c.688A>C (p.Ile230Leu)
c.706A>C (p.Ile236Leu)
 dbSNP gnomAD v3 gnomAD v4
3g.148741636A>GCA354888227AGTR1c.601A>G (p.Ile201Val)
c.688A>G (p.Ile230Val)
c.706A>G (p.Ile236Val)
3g.148741636A>TCA354888229AGTR1c.601A>T (p.Ile201Leu)
c.688A>T (p.Ile230Leu)
c.706A>T (p.Ile236Leu)
3g.148741637T>ACA354888232AGTR1c.602T>A (p.Ile201Lys)
c.689T>A (p.Ile230Lys)
c.707T>A (p.Ile236Lys)
3g.148741637T>CCA354888233AGTR1c.602T>C (p.Ile201Thr)
c.689T>C (p.Ile230Thr)
c.707T>C (p.Ile236Thr)
3g.148741637T>GCA354888235AGTR1c.602T>G (p.Ile201Arg)
c.689T>G (p.Ile230Arg)
c.707T>G (p.Ile236Arg)
3g.148741638A>CCA436389704AGTR1c.603A>C (p.Ile201=)
c.690A>C (p.Ile230=)
c.708A>C (p.Ile236=)
3g.148741638A>GCA354888237AGTR1c.603A>G (p.Ile201Met)
c.690A>G (p.Ile230Met)
c.708A>G (p.Ile236Met)
3g.148741638A>TCA436389705AGTR1c.603A>T (p.Ile201=)
c.690A>T (p.Ile230=)
c.708A>T (p.Ile236=)
3g.148741639C>ACA354888241AGTR1c.604C>A (p.Leu202Met)
c.691C>A (p.Leu231Met)
c.709C>A (p.Leu237Met)
 COSMIC
3g.148741639C=CA1409909961AGTR1c.604C= (p.Leu202=)
c.691C= (p.Leu231=)
c.709C= (p.Leu237=)
3g.148741639C>GCA354888242AGTR1c.604C>G (p.Leu202Val)
c.691C>G (p.Leu231Val)
c.709C>G (p.Leu237Val)
 gnomAD v4
3g.148741639C>TCA2657358AGTR1c.604C>T (p.Leu202=)
c.691C>T (p.Leu231=)
c.709C>T (p.Leu237=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741640T>ACA354888249AGTR1c.605T>A (p.Leu202Gln)
c.692T>A (p.Leu231Gln)
c.710T>A (p.Leu237Gln)
3g.148741640T>CCA354888245AGTR1c.605T>C (p.Leu202Pro)
c.692T>C (p.Leu231Pro)
c.710T>C (p.Leu237Pro)
 dbSNP
3g.148741640T>GCA354888247AGTR1c.605T>G (p.Leu202Arg)
c.692T>G (p.Leu231Arg)
c.710T>G (p.Leu237Arg)
3g.148741641G>ACA436389712AGTR1c.606G>A (p.Leu202=)
c.693G>A (p.Leu231=)
c.711G>A (p.Leu237=)
3g.148741641G>CCA436389714AGTR1c.606G>C (p.Leu202=)
c.693G>C (p.Leu231=)
c.711G>C (p.Leu237=)
3g.148741641G>TCA436389713AGTR1c.606G>T (p.Leu202=)
c.693G>T (p.Leu231=)
c.711G>T (p.Leu237=)
3g.148741642G>ACA354888250AGTR1c.607G>A (p.Gly203Ser)
c.694G>A (p.Gly232Ser)
c.712G>A (p.Gly238Ser)
 COSMIC
3g.148741642G>CCA354888252AGTR1c.607G>C (p.Gly203Arg)
c.694G>C (p.Gly232Arg)
c.712G>C (p.Gly238Arg)
3g.148741642G>TCA354888254AGTR1c.607G>T (p.Gly203Cys)
c.694G>T (p.Gly232Cys)
c.712G>T (p.Gly238Cys)
 gnomAD v4
3g.148741642_148741649delinsGGTTTCCTCA1409909964AGTR1c.607_614delinsGGTTTCCT (p.Gly203=)
c.694_701delinsGGTTTCCT (p.Gly232=)
c.712_719delinsGGTTTCCT (p.Gly238=)
3g.148741643G>ACA85497943AGTR1c.608G>A (p.Gly203Asp)
c.695G>A (p.Gly232Asp)
c.713G>A (p.Gly238Asp)
 dbSNP gnomAD v4
3g.148741643G>CCA354888257AGTR1c.608G>C (p.Gly203Ala)
c.695G>C (p.Gly232Ala)
c.713G>C (p.Gly238Ala)
3g.148741643G=CA1409909968AGTR1c.608G= (p.Gly203=)
c.695G= (p.Gly232=)
c.713G= (p.Gly238=)
3g.148741643G>TCA354888258AGTR1c.608G>T (p.Gly203Val)
c.695G>T (p.Gly232Val)
c.713G>T (p.Gly238Val)
3g.148741650_148741656delCA900490516AGTR1c.615_621del (p.Pro207Ter)
c.702_708del (p.Pro236Ter)
c.720_726del (p.Pro242Ter)
 dbSNP
3g.148741644T>ACA436389719AGTR1c.609T>A (p.Gly203=)
c.696T>A (p.Gly232=)
c.714T>A (p.Gly238=)
3g.148741644T>CCA10615489AGTR1c.609T>C (p.Gly203=)
c.696T>C (p.Gly232=)
c.714T>C (p.Gly238=)
 ClinVar dbSNP gnomAD v4
3g.148741644T>GCA436389722AGTR1c.609T>G (p.Gly203=)
c.696T>G (p.Gly232=)
c.714T>G (p.Gly238=)
3g.148741644T=CA1409909972AGTR1c.609T= (p.Gly203=)
c.696T= (p.Gly232=)
c.714T= (p.Gly238=)
3g.148741645T>ACA354888259AGTR1c.610T>A (p.Phe204Ile)
c.697T>A (p.Phe233Ile)
c.715T>A (p.Phe239Ile)
3g.148741645T>CCA354888261AGTR1c.610T>C (p.Phe204Leu)
c.697T>C (p.Phe233Leu)
c.715T>C (p.Phe239Leu)
3g.148741645T>GCA354888263AGTR1c.610T>G (p.Phe204Val)
c.697T>G (p.Phe233Val)
c.715T>G (p.Phe239Val)
3g.148741646T>ACA354888275AGTR1c.611T>A (p.Phe204Tyr)
c.698T>A (p.Phe233Tyr)
c.716T>A (p.Phe239Tyr)
3g.148741646T>CCA354888279AGTR1c.611T>C (p.Phe204Ser)
c.698T>C (p.Phe233Ser)
c.716T>C (p.Phe239Ser)
3g.148741646T>GCA354888273AGTR1c.611T>G (p.Phe204Cys)
c.698T>G (p.Phe233Cys)
c.716T>G (p.Phe239Cys)
3g.148741647C>ACA354888281AGTR1c.612C>A (p.Phe204Leu)
c.699C>A (p.Phe233Leu)
c.717C>A (p.Phe239Leu)
3g.148741647C>GCA354888283AGTR1c.612C>G (p.Phe204Leu)
c.699C>G (p.Phe233Leu)
c.717C>G (p.Phe239Leu)
3g.148741647C>TCA436389731AGTR1c.612C>T (p.Phe204=)
c.699C>T (p.Phe233=)
c.717C>T (p.Phe239=)
3g.148741648C>ACA354888289AGTR1c.613C>A (p.Leu205Met)
c.700C>A (p.Leu234Met)
c.718C>A (p.Leu240Met)
 COSMIC
3g.148741648C>GCA354888291AGTR1c.613C>G (p.Leu205Val)
c.700C>G (p.Leu234Val)
c.718C>G (p.Leu240Val)
3g.148741648C>TCA436389732AGTR1c.613C>T (p.Leu205=)
c.700C>T (p.Leu234=)
c.718C>T (p.Leu240=)
3g.148741649T>ACA354888296AGTR1c.614T>A (p.Leu205Gln)
c.701T>A (p.Leu234Gln)
c.719T>A (p.Leu240Gln)
3g.148741649T>CCA354888294AGTR1c.614T>C (p.Leu205Pro)
c.701T>C (p.Leu234Pro)
c.719T>C (p.Leu240Pro)
 dbSNP gnomAD v2 gnomAD v4
3g.148741649T>GCA354888293AGTR1c.614T>G (p.Leu205Arg)
c.701T>G (p.Leu234Arg)
c.719T>G (p.Leu240Arg)
3g.148741649T=CA1409909978AGTR1c.614T= (p.Leu205=)
c.701T= (p.Leu234=)
c.719T= (p.Leu240=)
3g.148741650G>ACA436389736AGTR1c.615G>A (p.Leu205=)
c.702G>A (p.Leu234=)
c.720G>A (p.Leu240=)
3g.148741650G>CCA85498018AGTR1c.615G>C (p.Leu205=)
c.702G>C (p.Leu234=)
c.720G>C (p.Leu240=)
 dbSNP gnomAD v3 gnomAD v4
3g.148741650G=CA1409909981AGTR1c.615G= (p.Leu205=)
c.702G= (p.Leu234=)
c.720G= (p.Leu240=)
3g.148741650G>TCA436389737AGTR1c.615G>T (p.Leu205=)
c.702G>T (p.Leu234=)
c.720G>T (p.Leu240=)
3g.148741651T>ACA354888301AGTR1c.616T>A (p.Phe206Ile)
c.703T>A (p.Phe235Ile)
c.721T>A (p.Phe241Ile)
3g.148741651T>CCA354888303AGTR1c.616T>C (p.Phe206Leu)
c.703T>C (p.Phe235Leu)
c.721T>C (p.Phe241Leu)
 gnomAD v4
3g.148741651T>GCA354888305AGTR1c.616T>G (p.Phe206Val)
c.703T>G (p.Phe235Val)
c.721T>G (p.Phe241Val)
3g.148741652T>ACA354888307AGTR1c.617T>A (p.Phe206Tyr)
c.704T>A (p.Phe235Tyr)
c.722T>A (p.Phe241Tyr)
3g.148741652T>CCA354888309AGTR1c.617T>C (p.Phe206Ser)
c.704T>C (p.Phe235Ser)
c.722T>C (p.Phe241Ser)
3g.148741652T>GCA354888313AGTR1c.617T>G (p.Phe206Cys)
c.704T>G (p.Phe235Cys)
c.722T>G (p.Phe241Cys)
3g.148741653T>ACA354888316AGTR1c.618T>A (p.Phe206Leu)
c.705T>A (p.Phe235Leu)
c.723T>A (p.Phe241Leu)
3g.148741653T>CCA436389743AGTR1c.618T>C (p.Phe206=)
c.705T>C (p.Phe235=)
c.723T>C (p.Phe241=)
3g.148741653T>GCA354888315AGTR1c.618T>G (p.Phe206Leu)
c.705T>G (p.Phe235Leu)
c.723T>G (p.Phe241Leu)
3g.148741654C>ACA354888318AGTR1c.619C>A (p.Pro207Thr)
c.706C>A (p.Pro236Thr)
c.724C>A (p.Pro242Thr)
3g.148741654C>GCA354888319AGTR1c.619C>G (p.Pro207Ala)
c.706C>G (p.Pro236Ala)
c.724C>G (p.Pro242Ala)
 gnomAD v4
3g.148741654C>TCA354888321AGTR1c.619C>T (p.Pro207Ser)
c.706C>T (p.Pro236Ser)
c.724C>T (p.Pro242Ser)
 COSMIC
3g.148741655C>ACA354888326AGTR1c.620C>A (p.Pro207His)
c.707C>A (p.Pro236His)
c.725C>A (p.Pro242His)
3g.148741655C>GCA354888328AGTR1c.620C>G (p.Pro207Arg)
c.707C>G (p.Pro236Arg)
c.725C>G (p.Pro242Arg)
3g.148741655C>TCA354888330AGTR1c.620C>T (p.Pro207Leu)
c.707C>T (p.Pro236Leu)
c.725C>T (p.Pro242Leu)
3g.148741656T>ACA436389753AGTR1c.621T>A (p.Pro207=)
c.708T>A (p.Pro236=)
c.726T>A (p.Pro242=)
3g.148741656T>CCA436389755AGTR1c.621T>C (p.Pro207=)
c.708T>C (p.Pro236=)
c.726T>C (p.Pro242=)
 COSMIC
3g.148741656T>GCA436389757AGTR1c.621T>G (p.Pro207=)
c.708T>G (p.Pro236=)
c.726T>G (p.Pro242=)
3g.148741657T>ACA354888336AGTR1c.622T>A (p.Phe208Ile)
c.709T>A (p.Phe237Ile)
c.727T>A (p.Phe243Ile)
3g.148741657T>CCA2657359AGTR1c.622T>C (p.Phe208Leu)
c.709T>C (p.Phe237Leu)
c.727T>C (p.Phe243Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741657T>GCA354888334AGTR1c.622T>G (p.Phe208Val)
c.709T>G (p.Phe237Val)
c.727T>G (p.Phe243Val)
3g.148741657T=CA1409909985AGTR1c.622T= (p.Phe208=)
c.709T= (p.Phe237=)
c.727T= (p.Phe243=)
3g.148741658T>ACA354888338AGTR1c.623T>A (p.Phe208Tyr)
c.710T>A (p.Phe237Tyr)
c.728T>A (p.Phe243Tyr)
3g.148741658T>CCA354888340AGTR1c.623T>C (p.Phe208Ser)
c.710T>C (p.Phe237Ser)
c.728T>C (p.Phe243Ser)
3g.148741658T>GCA354888342AGTR1c.623T>G (p.Phe208Cys)
c.710T>G (p.Phe237Cys)
c.728T>G (p.Phe243Cys)
3g.148741659T>ACA354888344AGTR1c.624T>A (p.Phe208Leu)
c.711T>A (p.Phe237Leu)
c.729T>A (p.Phe243Leu)
3g.148741659T>CCA436389764AGTR1c.624T>C (p.Phe208=)
c.711T>C (p.Phe237=)
c.729T>C (p.Phe243=)
3g.148741659T>GCA354888345AGTR1c.624T>G (p.Phe208Leu)
c.711T>G (p.Phe237Leu)
c.729T>G (p.Phe243Leu)
3g.148741660C>ACA354888349AGTR1c.625C>A (p.Leu209Met)
c.712C>A (p.Leu238Met)
c.730C>A (p.Leu244Met)
3g.148741660C=CA1409909990AGTR1c.625C= (p.Leu209=)
c.712C= (p.Leu238=)
c.730C= (p.Leu244=)
3g.148741660C>GCA354888348AGTR1c.625C>G (p.Leu209Val)
c.712C>G (p.Leu238Val)
c.730C>G (p.Leu244Val)
3g.148741660C>TCA2657360AGTR1c.625C>T (p.Leu209=)
c.712C>T (p.Leu238=)
c.730C>T (p.Leu244=)
 dbSNP ExAC gnomAD v3 gnomAD v4 COSMIC
3g.148741661T>ACA354888351AGTR1c.626T>A (p.Leu209Gln)
c.713T>A (p.Leu238Gln)
c.731T>A (p.Leu244Gln)
3g.148741661T>CCA354888352AGTR1c.626T>C (p.Leu209Pro)
c.713T>C (p.Leu238Pro)
c.731T>C (p.Leu244Pro)
3g.148741661T>GCA354888355AGTR1c.626T>G (p.Leu209Arg)
c.713T>G (p.Leu238Arg)
c.731T>G (p.Leu244Arg)
3g.148741662G>ACA436389770AGTR1c.627G>A (p.Leu209=)
c.714G>A (p.Leu238=)
c.732G>A (p.Leu244=)
3g.148741662G>CCA436389771AGTR1c.627G>C (p.Leu209=)
c.714G>C (p.Leu238=)
c.732G>C (p.Leu244=)
3g.148741662G>TCA436389772AGTR1c.627G>T (p.Leu209=)
c.714G>T (p.Leu238=)
c.732G>T (p.Leu244=)
3g.148741663A>CCA354888357AGTR1c.628A>C (p.Ile210Leu)
c.715A>C (p.Ile239Leu)
c.733A>C (p.Ile245Leu)
3g.148741663A>GCA354888359AGTR1c.628A>G (p.Ile210Val)
c.715A>G (p.Ile239Val)
c.733A>G (p.Ile245Val)
3g.148741663A>TCA354888361AGTR1c.628A>T (p.Ile210Phe)
c.715A>T (p.Ile239Phe)
c.733A>T (p.Ile245Phe)
3g.148741664T>ACA354888364AGTR1c.629T>A (p.Ile210Asn)
c.716T>A (p.Ile239Asn)
c.734T>A (p.Ile245Asn)
3g.148741664T>CCA354888366AGTR1c.629T>C (p.Ile210Thr)
c.716T>C (p.Ile239Thr)
c.734T>C (p.Ile245Thr)
3g.148741664T>GCA354888368AGTR1c.629T>G (p.Ile210Ser)
c.716T>G (p.Ile239Ser)
c.734T>G (p.Ile245Ser)
3g.148741665C>ACA436389780AGTR1c.630C>A (p.Ile210=)
c.717C>A (p.Ile239=)
c.735C>A (p.Ile245=)
 dbSNP
3g.148741665C=CA1409909993AGTR1c.630C= (p.Ile210=)
c.717C= (p.Ile239=)
c.735C= (p.Ile245=)
3g.148741665C>GCA354888370AGTR1c.630C>G (p.Ile210Met)
c.717C>G (p.Ile239Met)
c.735C>G (p.Ile245Met)
3g.148741665C>TCA436389781AGTR1c.630C>T (p.Ile210=)
c.717C>T (p.Ile239=)
c.735C>T (p.Ile245=)
3g.148741666A>CCA354888372AGTR1c.631A>C (p.Ile211Leu)
c.718A>C (p.Ile240Leu)
c.736A>C (p.Ile246Leu)
3g.148741666A>GCA354888374AGTR1c.631A>G (p.Ile211Val)
c.718A>G (p.Ile240Val)
c.736A>G (p.Ile246Val)
3g.148741666A>TCA354888375AGTR1c.631A>T (p.Ile211Phe)
c.718A>T (p.Ile240Phe)
c.736A>T (p.Ile246Phe)
3g.148741667T>ACA354888377AGTR1c.632T>A (p.Ile211Asn)
c.719T>A (p.Ile240Asn)
c.737T>A (p.Ile246Asn)
3g.148741667T>CCA354888380AGTR1c.632T>C (p.Ile211Thr)
c.719T>C (p.Ile240Thr)
c.737T>C (p.Ile246Thr)
3g.148741667T>GCA354888378AGTR1c.632T>G (p.Ile211Ser)
c.719T>G (p.Ile240Ser)
c.737T>G (p.Ile246Ser)
3g.148741668T>ACA436389786AGTR1c.633T>A (p.Ile211=)
c.720T>A (p.Ile240=)
c.738T>A (p.Ile246=)
3g.148741668T>CCA436389787AGTR1c.633T>C (p.Ile211=)
c.720T>C (p.Ile240=)
c.738T>C (p.Ile246=)
3g.148741668T>GCA354888382AGTR1c.633T>G (p.Ile211Met)
c.720T>G (p.Ile240Met)
c.738T>G (p.Ile246Met)
 gnomAD v4 COSMIC
3g.148741669C>ACA354888384AGTR1c.634C>A (p.Leu212Ile)
c.721C>A (p.Leu241Ile)
c.739C>A (p.Leu247Ile)
 COSMIC
3g.148741669C>GCA354888386AGTR1c.634C>G (p.Leu212Val)
c.721C>G (p.Leu241Val)
c.739C>G (p.Leu247Val)
3g.148741669C>TCA354888388AGTR1c.634C>T (p.Leu212Phe)
c.721C>T (p.Leu241Phe)
c.739C>T (p.Leu247Phe)
3g.148741670T>ACA354888391AGTR1c.635T>A (p.Leu212His)
c.722T>A (p.Leu241His)
c.740T>A (p.Leu247His)
 gnomAD v4
3g.148741670T>CCA354888392AGTR1c.635T>C (p.Leu212Pro)
c.722T>C (p.Leu241Pro)
c.740T>C (p.Leu247Pro)
3g.148741670T>GCA354888394AGTR1c.635T>G (p.Leu212Arg)
c.722T>G (p.Leu241Arg)
c.740T>G (p.Leu247Arg)
3g.148741671T>ACA436389795AGTR1c.636T>A (p.Leu212=)
c.723T>A (p.Leu241=)
c.741T>A (p.Leu247=)
3g.148741671T>CCA436389793AGTR1c.636T>C (p.Leu212=)
c.723T>C (p.Leu241=)
c.741T>C (p.Leu247=)
3g.148741671T>GCA436389790AGTR1c.636T>G (p.Leu212=)
c.723T>G (p.Leu241=)
c.741T>G (p.Leu247=)
3g.148741672A=CA1409909995AGTR1c.637A= (p.Thr213=)
c.724A= (p.Thr242=)
c.742A= (p.Thr248=)
3g.148741672A>CCA354888396AGTR1c.637A>C (p.Thr213Pro)
c.724A>C (p.Thr242Pro)
c.742A>C (p.Thr248Pro)
3g.148741672A>GCA354888398AGTR1c.637A>G (p.Thr213Ala)
c.724A>G (p.Thr242Ala)
c.742A>G (p.Thr248Ala)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.148741672A>TCA354888400AGTR1c.637A>T (p.Thr213Ser)
c.724A>T (p.Thr242Ser)
c.742A>T (p.Thr248Ser)
3g.148741673C>ACA354888403AGTR1c.638C>A (p.Thr213Lys)
c.725C>A (p.Thr242Lys)
c.743C>A (p.Thr248Lys)
 dbSNP gnomAD v3 gnomAD v4
3g.148741673C=CA1409909998AGTR1c.638C= (p.Thr213=)
c.725C= (p.Thr242=)
c.743C= (p.Thr248=)
3g.148741673C>GCA354888405AGTR1c.638C>G (p.Thr213Arg)
c.725C>G (p.Thr242Arg)
c.743C>G (p.Thr248Arg)
3g.148741673C>TCA354888407AGTR1c.638C>T (p.Thr213Ile)
c.725C>T (p.Thr242Ile)
c.743C>T (p.Thr248Ile)
 dbSNP

Number of alleles fetched