Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.148741422T>ACA436389699AGTR1c.387T>A (p.Ala129=)
c.474T>A (p.Ala158=)
c.492T>A (p.Ala164=)
3g.148741422T>CCA436389702AGTR1c.387T>C (p.Ala129=)
c.474T>C (p.Ala158=)
c.492T>C (p.Ala164=)
3g.148741422T>GCA436389701AGTR1c.387T>G (p.Ala129=)
c.474T>G (p.Ala158=)
c.492T>G (p.Ala164=)
3g.148741423A>CCA354887126AGTR1c.388A>C (p.Ile130Leu)
c.475A>C (p.Ile159Leu)
c.493A>C (p.Ile165Leu)
3g.148741423A>GCA354887129AGTR1c.388A>G (p.Ile130Val)
c.475A>G (p.Ile159Val)
c.493A>G (p.Ile165Val)
 gnomAD v4
3g.148741423A>TCA354887130AGTR1c.388A>T (p.Ile130Phe)
c.475A>T (p.Ile159Phe)
c.493A>T (p.Ile165Phe)
3g.148741424T>ACA354887135AGTR1c.389T>A (p.Ile130Asn)
c.476T>A (p.Ile159Asn)
c.494T>A (p.Ile165Asn)
3g.148741424T>CCA354887136AGTR1c.389T>C (p.Ile130Thr)
c.476T>C (p.Ile159Thr)
c.494T>C (p.Ile165Thr)
3g.148741424T>GCA354887138AGTR1c.389T>G (p.Ile130Ser)
c.476T>G (p.Ile159Ser)
c.494T>G (p.Ile165Ser)
3g.148741425T>ACA436389707AGTR1c.390T>A (p.Ile130=)
c.477T>A (p.Ile159=)
c.495T>A (p.Ile165=)
3g.148741425T>CCA436389708AGTR1c.390T>C (p.Ile130=)
c.477T>C (p.Ile159=)
c.495T>C (p.Ile165=)
3g.148741425T>GCA354887139AGTR1c.390T>G (p.Ile130Met)
c.477T>G (p.Ile159Met)
c.495T>G (p.Ile165Met)
3g.148741426G>ACA354887141AGTR1c.391G>A (p.Val131Ile)
c.478G>A (p.Val160Ile)
c.496G>A (p.Val166Ile)
3g.148741426G>CCA354887142AGTR1c.391G>C (p.Val131Leu)
c.478G>C (p.Val160Leu)
c.496G>C (p.Val166Leu)
3g.148741426G>TCA354887143AGTR1c.391G>T (p.Val131Phe)
c.478G>T (p.Val160Phe)
c.496G>T (p.Val166Phe)
3g.148741427T>ACA354887144AGTR1c.392T>A (p.Val131Asp)
c.479T>A (p.Val160Asp)
c.497T>A (p.Val166Asp)
3g.148741427T>CCA354887145AGTR1c.392T>C (p.Val131Ala)
c.479T>C (p.Val160Ala)
c.497T>C (p.Val166Ala)
3g.148741427T>GCA354887146AGTR1c.392T>G (p.Val131Gly)
c.479T>G (p.Val160Gly)
c.497T>G (p.Val166Gly)
3g.148741428T>ACA436389715AGTR1c.393T>A (p.Val131=)
c.480T>A (p.Val160=)
c.498T>A (p.Val166=)
3g.148741428T>CCA436389716AGTR1c.393T>C (p.Val131=)
c.480T>C (p.Val160=)
c.498T>C (p.Val166=)
3g.148741428T>GCA436389717AGTR1c.393T>G (p.Val131=)
c.480T>G (p.Val160=)
c.498T>G (p.Val166=)
3g.148741429C>ACA2657324AGTR1c.394C>A (p.His132Asn)
c.481C>A (p.His161Asn)
c.499C>A (p.His167Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.148741429C=CA1409909663AGTR1c.394C= (p.His132=)
c.481C= (p.His161=)
c.499C= (p.His167=)
3g.148741429C>GCA354887150AGTR1c.394C>G (p.His132Asp)
c.481C>G (p.His161Asp)
c.499C>G (p.His167Asp)
3g.148741429C>TCA354887153AGTR1c.394C>T (p.His132Tyr)
c.481C>T (p.His161Tyr)
c.499C>T (p.His167Tyr)
 COSMIC
3g.148741430A=CA1409909666AGTR1c.395A= (p.His132=)
c.482A= (p.His161=)
c.500A= (p.His167=)
3g.148741430A>CCA354887157AGTR1c.395A>C (p.His132Pro)
c.482A>C (p.His161Pro)
c.500A>C (p.His167Pro)
3g.148741430A>GCA354887159AGTR1c.395A>G (p.His132Arg)
c.482A>G (p.His161Arg)
c.500A>G (p.His167Arg)
3g.148741430A>TCA354887173AGTR1c.395A>T (p.His132Leu)
c.482A>T (p.His161Leu)
c.500A>T (p.His167Leu)
3g.148741431C>ACA354887175AGTR1c.396C>A (p.His132Gln)
c.483C>A (p.His161Gln)
c.501C>A (p.His167Gln)
3g.148741431C>GCA354887176AGTR1c.396C>G (p.His132Gln)
c.483C>G (p.His161Gln)
c.501C>G (p.His167Gln)
3g.148741431C>TCA436389721AGTR1c.396C>T (p.His132=)
c.483C>T (p.His161=)
c.501C>T (p.His167=)
3g.148741433dupCA547365419AGTR1c.398dup (p.Met134AsnfsTer?)
c.485dup (p.Met163AsnfsTer?)
c.503dup (p.Met169AsnfsTer?)
 dbSNP gnomAD v2 gnomAD v4
3g.148741432C>ACA354887191AGTR1c.397C>A (p.Pro133Thr)
c.484C>A (p.Pro162Thr)
c.502C>A (p.Pro168Thr)
 gnomAD v4
3g.148741432C>GCA354887179AGTR1c.397C>G (p.Pro133Ala)
c.484C>G (p.Pro162Ala)
c.502C>G (p.Pro168Ala)
3g.148741432C>TCA354887189AGTR1c.397C>T (p.Pro133Ser)
c.484C>T (p.Pro162Ser)
c.502C>T (p.Pro168Ser)
3g.148741433C>ACA354887193AGTR1c.398C>A (p.Pro133Gln)
c.485C>A (p.Pro162Gln)
c.503C>A (p.Pro168Gln)
3g.148741433C>GCA354887194AGTR1c.398C>G (p.Pro133Arg)
c.485C>G (p.Pro162Arg)
c.503C>G (p.Pro168Arg)
3g.148741433C>TCA354887197AGTR1c.398C>T (p.Pro133Leu)
c.485C>T (p.Pro162Leu)
c.503C>T (p.Pro168Leu)
3g.148741434A>CCA436389725AGTR1c.399A>C (p.Pro133=)
c.486A>C (p.Pro162=)
c.504A>C (p.Pro168=)
3g.148741434A>GCA436389727AGTR1c.399A>G (p.Pro133=)
c.486A>G (p.Pro162=)
c.504A>G (p.Pro168=)
3g.148741434A>TCA436389729AGTR1c.399A>T (p.Pro133=)
c.486A>T (p.Pro162=)
c.504A>T (p.Pro168=)
3g.148741435dupCA2668116560AGTR1c.400dup (p.Met134AsnfsTer?)
c.487dup (p.Met163AsnfsTer?)
c.505dup (p.Met169AsnfsTer?)
 gnomAD v4
3g.148741435A=CA1409909671AGTR1c.400A= (p.Met134=)
c.487A= (p.Met163=)
c.505A= (p.Met169=)
3g.148741435A>CCA354887200AGTR1c.400A>C (p.Met134Leu)
c.487A>C (p.Met163Leu)
c.505A>C (p.Met169Leu)
3g.148741435A>GCA2657325AGTR1c.400A>G (p.Met134Val)
c.487A>G (p.Met163Val)
c.505A>G (p.Met169Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741435A>TCA354887201AGTR1c.400A>T (p.Met134Leu)
c.487A>T (p.Met163Leu)
c.505A>T (p.Met169Leu)
 dbSNP gnomAD v2 gnomAD v4
3g.148741436T>ACA354887205AGTR1c.401T>A (p.Met134Lys)
c.488T>A (p.Met163Lys)
c.506T>A (p.Met169Lys)
3g.148741436T>CCA354887203AGTR1c.401T>C (p.Met134Thr)
c.488T>C (p.Met163Thr)
c.506T>C (p.Met169Thr)
 gnomAD v4
3g.148741436T>GCA354887202AGTR1c.401T>G (p.Met134Arg)
c.488T>G (p.Met163Arg)
c.506T>G (p.Met169Arg)
3g.148741437G>ACA354887208AGTR1c.402G>A (p.Met134Ile)
c.489G>A (p.Met163Ile)
c.507G>A (p.Met169Ile)
 dbSNP gnomAD v2 gnomAD v4
3g.148741437G>CCA354887209AGTR1c.402G>C (p.Met134Ile)
c.489G>C (p.Met163Ile)
c.507G>C (p.Met169Ile)
3g.148741437G=CA1409909676AGTR1c.402G= (p.Met134=)
c.489G= (p.Met163=)
c.507G= (p.Met169=)
3g.148741437G>TCA354887210AGTR1c.402G>T (p.Met134Ile)
c.489G>T (p.Met163Ile)
c.507G>T (p.Met169Ile)
3g.148741438A>CCA354887213AGTR1c.403A>C (p.Lys135Gln)
c.490A>C (p.Lys164Gln)
c.508A>C (p.Lys170Gln)
3g.148741438A>GCA354887218AGTR1c.403A>G (p.Lys135Glu)
c.490A>G (p.Lys164Glu)
c.508A>G (p.Lys170Glu)
3g.148741438A>TCA354887220AGTR1c.403A>T (p.Lys135Ter)
c.490A>T (p.Lys164Ter)
c.508A>T (p.Lys170Ter)
3g.148741439A>CCA354887223AGTR1c.404A>C (p.Lys135Thr)
c.491A>C (p.Lys164Thr)
c.509A>C (p.Lys170Thr)
3g.148741439A>GCA354887229AGTR1c.404A>G (p.Lys135Arg)
c.491A>G (p.Lys164Arg)
c.509A>G (p.Lys170Arg)
3g.148741439A>TCA354887228AGTR1c.404A>T (p.Lys135Met)
c.491A>T (p.Lys164Met)
c.509A>T (p.Lys170Met)
 dbSNP
3g.148741440G>ACA436389741AGTR1c.405G>A (p.Lys135=)
c.492G>A (p.Lys164=)
c.510G>A (p.Lys170=)
 gnomAD v4
3g.148741440G>CCA354887231AGTR1c.405G>C (p.Lys135Asn)
c.492G>C (p.Lys164Asn)
c.510G>C (p.Lys170Asn)
3g.148741440G>TCA354887234AGTR1c.405G>T (p.Lys135Asn)
c.492G>T (p.Lys164Asn)
c.510G>T (p.Lys170Asn)
3g.148741441T>ACA354887237AGTR1c.406T>A (p.Ser136Thr)
c.493T>A (p.Ser165Thr)
c.511T>A (p.Ser171Thr)
3g.148741441T>CCA354887240AGTR1c.406T>C (p.Ser136Pro)
c.493T>C (p.Ser165Pro)
c.511T>C (p.Ser171Pro)
3g.148741441T>GCA354887243AGTR1c.406T>G (p.Ser136Ala)
c.493T>G (p.Ser165Ala)
c.511T>G (p.Ser171Ala)
3g.148741442C>ACA2657326AGTR1c.407C>A (p.Ser136Tyr)
c.494C>A (p.Ser165Tyr)
c.512C>A (p.Ser171Tyr)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741442C=CA1409909680AGTR1c.407C= (p.Ser136=)
c.494C= (p.Ser165=)
c.512C= (p.Ser171=)
3g.148741442C>GCA354887246AGTR1c.407C>G (p.Ser136Cys)
c.494C>G (p.Ser165Cys)
c.512C>G (p.Ser171Cys)
3g.148741442C>TCA354887247AGTR1c.407C>T (p.Ser136Phe)
c.494C>T (p.Ser165Phe)
c.512C>T (p.Ser171Phe)
3g.148741443C>ACA436389745AGTR1c.408C>A (p.Ser136=)
c.495C>A (p.Ser165=)
c.513C>A (p.Ser171=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.148741443C=CA1409909683AGTR1c.408C= (p.Ser136=)
c.495C= (p.Ser165=)
c.513C= (p.Ser171=)
3g.148741443C>GCA436389747AGTR1c.408C>G (p.Ser136=)
c.495C>G (p.Ser165=)
c.513C>G (p.Ser171=)
3g.148741443C>TCA436389748AGTR1c.408C>T (p.Ser136=)
c.495C>T (p.Ser165=)
c.513C>T (p.Ser171=)
3g.148741444C>ACA354887249AGTR1c.409C>A (p.Arg137Ser)
c.496C>A (p.Arg166Ser)
c.514C>A (p.Arg172Ser)
3g.148741444C=CA1409909690AGTR1c.409C= (p.Arg137=)
c.496C= (p.Arg166=)
c.514C= (p.Arg172=)
3g.148741444C>GCA354887251AGTR1c.409C>G (p.Arg137Gly)
c.496C>G (p.Arg166Gly)
c.514C>G (p.Arg172Gly)
3g.148741444C>TCA85497688AGTR1c.409C>T (p.Arg137Cys)
c.496C>T (p.Arg166Cys)
c.514C>T (p.Arg172Cys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.148741445G>ACA2657327AGTR1c.410G>A (p.Arg137His)
c.497G>A (p.Arg166His)
c.515G>A (p.Arg172His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741445G>CCA354887265AGTR1c.410G>C (p.Arg137Pro)
c.497G>C (p.Arg166Pro)
c.515G>C (p.Arg172Pro)
3g.148741445G=CA1409909693AGTR1c.410G= (p.Arg137=)
c.497G= (p.Arg166=)
c.515G= (p.Arg172=)
3g.148741445G>TCA354887262AGTR1c.410G>T (p.Arg137Leu)
c.497G>T (p.Arg166Leu)
c.515G>T (p.Arg172Leu)
3g.148741446C>ACA436389752AGTR1c.411C>A (p.Arg137=)
c.498C>A (p.Arg166=)
c.516C>A (p.Arg172=)
 gnomAD v4
3g.148741446C>GCA436389754AGTR1c.411C>G (p.Arg137=)
c.498C>G (p.Arg166=)
c.516C>G (p.Arg172=)
3g.148741446C>TCA436389756AGTR1c.411C>T (p.Arg137=)
c.498C>T (p.Arg166=)
c.516C>T (p.Arg172=)
3g.148741447C>ACA354887267AGTR1c.412C>A (p.Leu138Ile)
c.499C>A (p.Leu167Ile)
c.517C>A (p.Leu173Ile)
3g.148741447C>GCA354887271AGTR1c.412C>G (p.Leu138Val)
c.499C>G (p.Leu167Val)
c.517C>G (p.Leu173Val)
3g.148741447C>TCA354887269AGTR1c.412C>T (p.Leu138Phe)
c.499C>T (p.Leu167Phe)
c.517C>T (p.Leu173Phe)
3g.148741448T>ACA354887273AGTR1c.413T>A (p.Leu138His)
c.500T>A (p.Leu167His)
c.518T>A (p.Leu173His)
3g.148741448T>CCA354887276AGTR1c.413T>C (p.Leu138Pro)
c.500T>C (p.Leu167Pro)
c.518T>C (p.Leu173Pro)
3g.148741448T>GCA354887278AGTR1c.413T>G (p.Leu138Arg)
c.500T>G (p.Leu167Arg)
c.518T>G (p.Leu173Arg)
3g.148741449T>ACA436389760AGTR1c.414T>A (p.Leu138=)
c.501T>A (p.Leu167=)
c.519T>A (p.Leu173=)
3g.148741449T>CCA436389761AGTR1c.414T>C (p.Leu138=)
c.501T>C (p.Leu167=)
c.519T>C (p.Leu173=)
3g.148741449T>GCA436389763AGTR1c.414T>G (p.Leu138=)
c.501T>G (p.Leu167=)
c.519T>G (p.Leu173=)
3g.148741450C>ACA436389766AGTR1c.415C>A (p.Arg139=)
c.502C>A (p.Arg168=)
c.520C>A (p.Arg174=)
3g.148741450C=CA1409909695AGTR1c.415C= (p.Arg139=)
c.502C= (p.Arg168=)
c.520C= (p.Arg174=)
3g.148741450C>GCA354887280AGTR1c.415C>G (p.Arg139Gly)
c.502C>G (p.Arg168Gly)
c.520C>G (p.Arg174Gly)
3g.148741450C>TCA354887281AGTR1c.415C>T (p.Arg139Ter)
c.502C>T (p.Arg168Ter)
c.520C>T (p.Arg174Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
3g.148741451G>ACA2657328AGTR1c.416G>A (p.Arg139Gln)
c.503G>A (p.Arg168Gln)
c.521G>A (p.Arg174Gln)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741451G>CCA354887283AGTR1c.416G>C (p.Arg139Pro)
c.503G>C (p.Arg168Pro)
c.521G>C (p.Arg174Pro)
3g.148741451G=CA1409909698AGTR1c.416G= (p.Arg139=)
c.503G= (p.Arg168=)
c.521G= (p.Arg174=)
3g.148741451G>TCA354887284AGTR1c.416G>T (p.Arg139Leu)
c.503G>T (p.Arg168Leu)
c.521G>T (p.Arg174Leu)
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)

Number of alleles fetched