Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.148741725_148741727delCA900490700AGTR1c.690_692del (p.Lys230del)
c.777_779del (p.Lys259del)
c.795_797del (p.Lys265del)
 dbSNP gnomAD v3 gnomAD v4
3g.148741727A=CA1409910071AGTR1c.692A= (p.Asn231=)
c.779A= (p.Asn260=)
c.797A= (p.Asn266=)
3g.148741727A>CCA2657365AGTR1c.692A>C (p.Asn231Thr)
c.779A>C (p.Asn260Thr)
c.797A>C (p.Asn266Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741727A>GCA354888653AGTR1c.692A>G (p.Asn231Ser)
c.779A>G (p.Asn260Ser)
c.797A>G (p.Asn266Ser)
 gnomAD v4
3g.148741727A>TCA354888654AGTR1c.692A>T (p.Asn231Ile)
c.779A>T (p.Asn260Ile)
c.797A>T (p.Asn266Ile)
3g.148741728C>ACA354888658AGTR1c.693C>A (p.Asn231Lys)
c.780C>A (p.Asn260Lys)
c.798C>A (p.Asn266Lys)
3g.148741728C=CA1409910074AGTR1c.693C= (p.Asn231=)
c.780C= (p.Asn260=)
c.798C= (p.Asn266=)
3g.148741728C>GCA354888661AGTR1c.693C>G (p.Asn231Lys)
c.780C>G (p.Asn260Lys)
c.798C>G (p.Asn266Lys)
3g.148741728C>TCA436389938AGTR1c.693C>T (p.Asn231=)
c.780C>T (p.Asn260=)
c.798C>T (p.Asn266=)
 dbSNP
3g.148741731_148741735delCA2499216539AGTR1c.696_700del (p.Pro233LysfsTer2)
c.783_787del (p.Pro262LysfsTer2)
c.801_805del (p.Pro268LysfsTer2)
 ClinVar dbSNP gnomAD v4
3g.148741729A>CCA354888663AGTR1c.694A>C (p.Lys232Gln)
c.781A>C (p.Lys261Gln)
c.799A>C (p.Lys267Gln)
3g.148741729A>GCA354888664AGTR1c.694A>G (p.Lys232Glu)
c.781A>G (p.Lys261Glu)
c.799A>G (p.Lys267Glu)
3g.148741729A>TCA354888666AGTR1c.694A>T (p.Lys232Ter)
c.781A>T (p.Lys261Ter)
c.799A>T (p.Lys267Ter)
3g.148741730A>CCA354888668AGTR1c.695A>C (p.Lys232Thr)
c.782A>C (p.Lys261Thr)
c.800A>C (p.Lys267Thr)
3g.148741730A>GCA354888669AGTR1c.695A>G (p.Lys232Arg)
c.782A>G (p.Lys261Arg)
c.800A>G (p.Lys267Arg)
3g.148741730A>TCA354888671AGTR1c.695A>T (p.Lys232Ile)
c.782A>T (p.Lys261Ile)
c.800A>T (p.Lys267Ile)
3g.148741731A>CCA354888673AGTR1c.696A>C (p.Lys232Asn)
c.783A>C (p.Lys261Asn)
c.801A>C (p.Lys267Asn)
3g.148741731A>GCA436389942AGTR1c.696A>G (p.Lys232=)
c.783A>G (p.Lys261=)
c.801A>G (p.Lys267=)
 gnomAD v4
3g.148741731A>TCA354888675AGTR1c.696A>T (p.Lys232Asn)
c.783A>T (p.Lys261Asn)
c.801A>T (p.Lys267Asn)
3g.148741732C>ACA2657366AGTR1c.697C>A (p.Pro233Thr)
c.784C>A (p.Pro262Thr)
c.802C>A (p.Pro268Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741732C=CA1409910078AGTR1c.697C= (p.Pro233=)
c.784C= (p.Pro262=)
c.802C= (p.Pro268=)
3g.148741732C>GCA354888678AGTR1c.697C>G (p.Pro233Ala)
c.784C>G (p.Pro262Ala)
c.802C>G (p.Pro268Ala)
3g.148741732C>TCA354888680AGTR1c.697C>T (p.Pro233Ser)
c.784C>T (p.Pro262Ser)
c.802C>T (p.Pro268Ser)
3g.148741733C>ACA354888682AGTR1c.698C>A (p.Pro233Gln)
c.785C>A (p.Pro262Gln)
c.803C>A (p.Pro268Gln)
3g.148741733C>GCA354888686AGTR1c.698C>G (p.Pro233Arg)
c.785C>G (p.Pro262Arg)
c.803C>G (p.Pro268Arg)
3g.148741733C>TCA354888684AGTR1c.698C>T (p.Pro233Leu)
c.785C>T (p.Pro262Leu)
c.803C>T (p.Pro268Leu)
3g.148741734A>CCA436389950AGTR1c.699A>C (p.Pro233=)
c.786A>C (p.Pro262=)
c.804A>C (p.Pro268=)
3g.148741734A>GCA436389951AGTR1c.699A>G (p.Pro233=)
c.786A>G (p.Pro262=)
c.804A>G (p.Pro268=)
3g.148741734A>TCA436389952AGTR1c.699A>T (p.Pro233=)
c.786A>T (p.Pro262=)
c.804A>T (p.Pro268=)
3g.148741734_148741735insCCAAACACACCCAACACCA2758831181AGTR1c.699_700insCCAAACACACCCAACAC (p.Arg234ProfsTer14)
c.786_787insCCAAACACACCCAACAC (p.Arg263ProfsTer14)
c.804_805insCCAAACACACCCAACAC (p.Arg269ProfsTer14)
3g.148741735A>CCA436389955AGTR1c.700A>C (p.Arg234=)
c.787A>C (p.Arg263=)
c.805A>C (p.Arg269=)
3g.148741735A>GCA354888689AGTR1c.700A>G (p.Arg234Gly)
c.787A>G (p.Arg263Gly)
c.805A>G (p.Arg269Gly)
3g.148741735A>TCA354888692AGTR1c.700A>T (p.Arg234Ter)
c.787A>T (p.Arg263Ter)
c.805A>T (p.Arg269Ter)
3g.148741736G>ACA354888693AGTR1c.701G>A (p.Arg234Lys)
c.788G>A (p.Arg263Lys)
c.806G>A (p.Arg269Lys)
3g.148741736G>CCA85498189AGTR1c.701G>C (p.Arg234Thr)
c.788G>C (p.Arg263Thr)
c.806G>C (p.Arg269Thr)
 dbSNP gnomAD v2
3g.148741736G=CA1409910084AGTR1c.701G= (p.Arg234=)
c.788G= (p.Arg263=)
c.806G= (p.Arg269=)
3g.148741736G>TCA354888694AGTR1c.701G>T (p.Arg234Ile)
c.788G>T (p.Arg263Ile)
c.806G>T (p.Arg269Ile)
 COSMIC
3g.148741737A>CCA354888695AGTR1c.702A>C (p.Arg234Ser)
c.789A>C (p.Arg263Ser)
c.807A>C (p.Arg269Ser)
3g.148741737A>GCA436389962AGTR1c.702A>G (p.Arg234=)
c.789A>G (p.Arg263=)
c.807A>G (p.Arg269=)
 COSMIC
3g.148741737A>TCA354888696AGTR1c.702A>T (p.Arg234Ser)
c.789A>T (p.Arg263Ser)
c.807A>T (p.Arg269Ser)
3g.148741739dupCA85498196AGTR1c.704dup (p.Asn235LysfsTer2)
c.791dup (p.Asn264LysfsTer2)
c.809dup (p.Asn270LysfsTer2)
 dbSNP
3g.148741738A>CCA354888701AGTR1c.703A>C (p.Asn235His)
c.790A>C (p.Asn264His)
c.808A>C (p.Asn270His)
3g.148741738A>GCA354888704AGTR1c.703A>G (p.Asn235Asp)
c.790A>G (p.Asn264Asp)
c.808A>G (p.Asn270Asp)
3g.148741738A>TCA354888705AGTR1c.703A>T (p.Asn235Tyr)
c.790A>T (p.Asn264Tyr)
c.808A>T (p.Asn270Tyr)
3g.148741739A>CCA354888706AGTR1c.704A>C (p.Asn235Thr)
c.791A>C (p.Asn264Thr)
c.809A>C (p.Asn270Thr)
3g.148741739A>GCA354888707AGTR1c.704A>G (p.Asn235Ser)
c.791A>G (p.Asn264Ser)
c.809A>G (p.Asn270Ser)
3g.148741739A>TCA354888708AGTR1c.704A>T (p.Asn235Ile)
c.791A>T (p.Asn264Ile)
c.809A>T (p.Asn270Ile)
3g.148741740T>ACA354888711AGTR1c.705T>A (p.Asn235Lys)
c.792T>A (p.Asn264Lys)
c.810T>A (p.Asn270Lys)
 gnomAD v4
3g.148741740T>CCA2657367AGTR1c.705T>C (p.Asn235=)
c.792T>C (p.Asn264=)
c.810T>C (p.Asn270=)
 dbSNP ExAC gnomAD v2
3g.148741740T>GCA354888714AGTR1c.705T>G (p.Asn235Lys)
c.792T>G (p.Asn264Lys)
c.810T>G (p.Asn270Lys)
3g.148741740T=CA1409910095AGTR1c.705T= (p.Asn235=)
c.792T= (p.Asn264=)
c.810T= (p.Asn270=)
3g.148741741G>ACA354888719AGTR1c.706G>A (p.Asp236Asn)
c.793G>A (p.Asp265Asn)
c.811G>A (p.Asp271Asn)
3g.148741741G>CCA2657368AGTR1c.706G>C (p.Asp236His)
c.793G>C (p.Asp265His)
c.811G>C (p.Asp271His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741741G=CA1409910098AGTR1c.706G= (p.Asp236=)
c.793G= (p.Asp265=)
c.811G= (p.Asp271=)
3g.148741741G>TCA354888722AGTR1c.706G>T (p.Asp236Tyr)
c.793G>T (p.Asp265Tyr)
c.811G>T (p.Asp271Tyr)
 dbSNP gnomAD v2 gnomAD v4
3g.148741742A=CA1409910101AGTR1c.707A= (p.Asp236=)
c.794A= (p.Asp265=)
c.812A= (p.Asp271=)
3g.148741742A>CCA2657369AGTR1c.707A>C (p.Asp236Ala)
c.794A>C (p.Asp265Ala)
c.812A>C (p.Asp271Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741742A>GCA354888726AGTR1c.707A>G (p.Asp236Gly)
c.794A>G (p.Asp265Gly)
c.812A>G (p.Asp271Gly)
 gnomAD v4
3g.148741742A>TCA354888728AGTR1c.707A>T (p.Asp236Val)
c.794A>T (p.Asp265Val)
c.812A>T (p.Asp271Val)
 ClinVar dbSNP
3g.148741743T>ACA354888731AGTR1c.708T>A (p.Asp236Glu)
c.795T>A (p.Asp265Glu)
c.813T>A (p.Asp271Glu)
3g.148741743T>CCA436389976AGTR1c.708T>C (p.Asp236=)
c.795T>C (p.Asp265=)
c.813T>C (p.Asp271=)
3g.148741743T>GCA2657370AGTR1c.708T>G (p.Asp236Glu)
c.795T>G (p.Asp265Glu)
c.813T>G (p.Asp271Glu)
 dbSNP ExAC gnomAD v2
3g.148741743T=CA1409910103AGTR1c.708T= (p.Asp236=)
c.795T= (p.Asp265=)
c.813T= (p.Asp271=)
3g.148741744G>ACA354888735AGTR1c.709G>A (p.Asp237Asn)
c.796G>A (p.Asp266Asn)
c.814G>A (p.Asp272Asn)
 COSMIC
3g.148741744G>CCA354888736AGTR1c.709G>C (p.Asp237His)
c.796G>C (p.Asp266His)
c.814G>C (p.Asp272His)
3g.148741744G=CA1409910106AGTR1c.709G= (p.Asp237=)
c.796G= (p.Asp266=)
c.814G= (p.Asp272=)
3g.148741744G>TCA354888738AGTR1c.709G>T (p.Asp237Tyr)
c.796G>T (p.Asp266Tyr)
c.814G>T (p.Asp272Tyr)
 dbSNP gnomAD v2 gnomAD v4
3g.148741745A>CCA354888742AGTR1c.710A>C (p.Asp237Ala)
c.797A>C (p.Asp266Ala)
c.815A>C (p.Asp272Ala)
3g.148741745A>GCA354888743AGTR1c.710A>G (p.Asp237Gly)
c.797A>G (p.Asp266Gly)
c.815A>G (p.Asp272Gly)
3g.148741745A>TCA354888740AGTR1c.710A>T (p.Asp237Val)
c.797A>T (p.Asp266Val)
c.815A>T (p.Asp272Val)
3g.148741746T>ACA2657371AGTR1c.711T>A (p.Asp237Glu)
c.798T>A (p.Asp266Glu)
c.816T>A (p.Asp272Glu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741746T>CCA436389981AGTR1c.711T>C (p.Asp237=)
c.798T>C (p.Asp266=)
c.816T>C (p.Asp272=)
 gnomAD v4
3g.148741746T>GCA354888744AGTR1c.711T>G (p.Asp237Glu)
c.798T>G (p.Asp266Glu)
c.816T>G (p.Asp272Glu)
3g.148741746T=CA1409910110AGTR1c.711T= (p.Asp237=)
c.798T= (p.Asp266=)
c.816T= (p.Asp272=)
3g.148741746_148741747delinsTACA1409910113AGTR1c.711_712delinsTA (p.Asp237=)
c.798_799delinsTA (p.Asp266=)
c.816_817delinsTA (p.Asp272=)
3g.148741747delCA547365420AGTR1c.712del (p.Ile238PhefsTer4)
c.799del (p.Ile267PhefsTer4)
c.817del (p.Ile273PhefsTer4)
 dbSNP gnomAD v2
3g.148741747A>CCA354888748AGTR1c.712A>C (p.Ile238Leu)
c.799A>C (p.Ile267Leu)
c.817A>C (p.Ile273Leu)
3g.148741747A>GCA354888750AGTR1c.712A>G (p.Ile238Val)
c.799A>G (p.Ile267Val)
c.817A>G (p.Ile273Val)
3g.148741747A>TCA354888752AGTR1c.712A>T (p.Ile238Phe)
c.799A>T (p.Ile267Phe)
c.817A>T (p.Ile273Phe)
3g.148741748T>ACA354888754AGTR1c.713T>A (p.Ile238Asn)
c.800T>A (p.Ile267Asn)
c.818T>A (p.Ile273Asn)
3g.148741748T>CCA354888757AGTR1c.713T>C (p.Ile238Thr)
c.800T>C (p.Ile267Thr)
c.818T>C (p.Ile273Thr)
3g.148741748T>GCA354888760AGTR1c.713T>G (p.Ile238Ser)
c.800T>G (p.Ile267Ser)
c.818T>G (p.Ile273Ser)
3g.148741752delCA436389991AGTR1c.717del (p.Phe239LeufsTer3)
c.804del (p.Phe268LeufsTer3)
c.822del (p.Phe274LeufsTer3)
 COSMIC
3g.148741749T>ACA436389994AGTR1c.714T>A (p.Ile238=)
c.801T>A (p.Ile267=)
c.819T>A (p.Ile273=)
 gnomAD v4
3g.148741749T>CCA436389996AGTR1c.714T>C (p.Ile238=)
c.801T>C (p.Ile267=)
c.819T>C (p.Ile273=)
3g.148741749T>GCA354888762AGTR1c.714T>G (p.Ile238Met)
c.801T>G (p.Ile267Met)
c.819T>G (p.Ile273Met)
3g.148741750T>ACA354888767AGTR1c.715T>A (p.Phe239Ile)
c.802T>A (p.Phe268Ile)
c.820T>A (p.Phe274Ile)
3g.148741750T>CCA354888770AGTR1c.715T>C (p.Phe239Leu)
c.802T>C (p.Phe268Leu)
c.820T>C (p.Phe274Leu)
3g.148741750T>GCA354888775AGTR1c.715T>G (p.Phe239Val)
c.802T>G (p.Phe268Val)
c.820T>G (p.Phe274Val)
 gnomAD v4
3g.148741751T>ACA354888780AGTR1c.716T>A (p.Phe239Tyr)
c.803T>A (p.Phe268Tyr)
c.821T>A (p.Phe274Tyr)
3g.148741751T>CCA354888781AGTR1c.716T>C (p.Phe239Ser)
c.803T>C (p.Phe268Ser)
c.821T>C (p.Phe274Ser)
3g.148741751T>GCA354888782AGTR1c.716T>G (p.Phe239Cys)
c.803T>G (p.Phe268Cys)
c.821T>G (p.Phe274Cys)
3g.148741752T>ACA354888784AGTR1c.717T>A (p.Phe239Leu)
c.804T>A (p.Phe268Leu)
c.822T>A (p.Phe274Leu)
3g.148741752T>CCA436390007AGTR1c.717T>C (p.Phe239=)
c.804T>C (p.Phe268=)
c.822T>C (p.Phe274=)
3g.148741752T>GCA354888783AGTR1c.717T>G (p.Phe239Leu)
c.804T>G (p.Phe268Leu)
c.822T>G (p.Phe274Leu)
3g.148741753A>CCA354888785AGTR1c.718A>C (p.Lys240Gln)
c.805A>C (p.Lys269Gln)
c.823A>C (p.Lys275Gln)
3g.148741753A>GCA354888786AGTR1c.718A>G (p.Lys240Glu)
c.805A>G (p.Lys269Glu)
c.823A>G (p.Lys275Glu)
3g.148741753A>TCA354888787AGTR1c.718A>T (p.Lys240Ter)
c.805A>T (p.Lys269Ter)
c.823A>T (p.Lys275Ter)
3g.148741754A>CCA354888789AGTR1c.719A>C (p.Lys240Thr)
c.806A>C (p.Lys269Thr)
c.824A>C (p.Lys275Thr)
 COSMIC
3g.148741754A>GCA354888790AGTR1c.719A>G (p.Lys240Arg)
c.806A>G (p.Lys269Arg)
c.824A>G (p.Lys275Arg)
3g.148741754A>TCA354888791AGTR1c.719A>T (p.Lys240Met)
c.806A>T (p.Lys269Met)
c.824A>T (p.Lys275Met)
3g.148741755G>ACA436390012AGTR1c.720G>A (p.Lys240=)
c.807G>A (p.Lys269=)
c.825G>A (p.Lys275=)
 dbSNP
3g.148741755G>CCA354888794AGTR1c.720G>C (p.Lys240Asn)
c.807G>C (p.Lys269Asn)
c.825G>C (p.Lys275Asn)
3g.148741755G=CA1409910116AGTR1c.720G= (p.Lys240=)
c.807G= (p.Lys269=)
c.825G= (p.Lys275=)
3g.148741755G>TCA2657372AGTR1c.720G>T (p.Lys240Asn)
c.807G>T (p.Lys269Asn)
c.825G>T (p.Lys275Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741756A>CCA354888801AGTR1c.721A>C (p.Ile241Leu)
c.808A>C (p.Ile270Leu)
c.826A>C (p.Ile276Leu)
3g.148741756A>GCA354888802AGTR1c.721A>G (p.Ile241Val)
c.808A>G (p.Ile270Val)
c.826A>G (p.Ile276Val)
3g.148741756A>TCA354888803AGTR1c.721A>T (p.Ile241Leu)
c.808A>T (p.Ile270Leu)
c.826A>T (p.Ile276Leu)
3g.148741757T>ACA354888805AGTR1c.722T>A (p.Ile241Lys)
c.809T>A (p.Ile270Lys)
c.827T>A (p.Ile276Lys)
3g.148741757T>CCA354888806AGTR1c.722T>C (p.Ile241Thr)
c.809T>C (p.Ile270Thr)
c.827T>C (p.Ile276Thr)
 dbSNP gnomAD v4
3g.148741757T>GCA354888809AGTR1c.722T>G (p.Ile241Arg)
c.809T>G (p.Ile270Arg)
c.827T>G (p.Ile276Arg)
3g.148741757T=CA1409910119AGTR1c.722T= (p.Ile241=)
c.809T= (p.Ile270=)
c.827T= (p.Ile276=)
3g.148741758A>CCA436390019AGTR1c.723A>C (p.Ile241=)
c.810A>C (p.Ile270=)
c.828A>C (p.Ile276=)
3g.148741758A>GCA354888817AGTR1c.723A>G (p.Ile241Met)
c.810A>G (p.Ile270Met)
c.828A>G (p.Ile276Met)
3g.148741758A>TCA436390022AGTR1c.723A>T (p.Ile241=)
c.810A>T (p.Ile270=)
c.828A>T (p.Ile276=)
3g.148741759A>CCA354888820AGTR1c.724A>C (p.Ile242Leu)
c.811A>C (p.Ile271Leu)
c.829A>C (p.Ile277Leu)
3g.148741759A>GCA354888818AGTR1c.724A>G (p.Ile242Val)
c.811A>G (p.Ile271Val)
c.829A>G (p.Ile277Val)
3g.148741759A>TCA354888819AGTR1c.724A>T (p.Ile242Phe)
c.811A>T (p.Ile271Phe)
c.829A>T (p.Ile277Phe)
3g.148741760T>ACA354888821AGTR1c.725T>A (p.Ile242Asn)
c.812T>A (p.Ile271Asn)
c.830T>A (p.Ile277Asn)
3g.148741760T>CCA2657373AGTR1c.725T>C (p.Ile242Thr)
c.812T>C (p.Ile271Thr)
c.830T>C (p.Ile277Thr)
 dbSNP ExAC gnomAD v3 gnomAD v4
3g.148741760T>GCA354888824AGTR1c.725T>G (p.Ile242Ser)
c.812T>G (p.Ile271Ser)
c.830T>G (p.Ile277Ser)
3g.148741760T=CA1409910123AGTR1c.725T= (p.Ile242=)
c.812T= (p.Ile271=)
c.830T= (p.Ile277=)
3g.148741761T>ACA436390035AGTR1c.726T>A (p.Ile242=)
c.813T>A (p.Ile271=)
c.831T>A (p.Ile277=)
3g.148741761T>CCA436390034AGTR1c.726T>C (p.Ile242=)
c.813T>C (p.Ile271=)
c.831T>C (p.Ile277=)
 gnomAD v4
3g.148741761T>GCA354888826AGTR1c.726T>G (p.Ile242Met)
c.813T>G (p.Ile271Met)
c.831T>G (p.Ile277Met)
3g.148741762A>CCA354888829AGTR1c.727A>C (p.Met243Leu)
c.814A>C (p.Met272Leu)
c.832A>C (p.Met278Leu)
3g.148741762A>GCA354888833AGTR1c.727A>G (p.Met243Val)
c.814A>G (p.Met272Val)
c.832A>G (p.Met278Val)
3g.148741762A>TCA354888835AGTR1c.727A>T (p.Met243Leu)
c.814A>T (p.Met272Leu)
c.832A>T (p.Met278Leu)
3g.148741763T>ACA354888837AGTR1c.728T>A (p.Met243Lys)
c.815T>A (p.Met272Lys)
c.833T>A (p.Met278Lys)
3g.148741763T>CCA354888838AGTR1c.728T>C (p.Met243Thr)
c.815T>C (p.Met272Thr)
c.833T>C (p.Met278Thr)
 COSMIC
3g.148741763T>GCA354888840AGTR1c.728T>G (p.Met243Arg)
c.815T>G (p.Met272Arg)
c.833T>G (p.Met278Arg)
3g.148741764G>ACA354888845AGTR1c.729G>A (p.Met243Ile)
c.816G>A (p.Met272Ile)
c.834G>A (p.Met278Ile)
 gnomAD v4
3g.148741764G>CCA2657374AGTR1c.729G>C (p.Met243Ile)
c.816G>C (p.Met272Ile)
c.834G>C (p.Met278Ile)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741764G=CA1409910126AGTR1c.729G= (p.Met243=)
c.816G= (p.Met272=)
c.834G= (p.Met278=)
3g.148741764G>TCA354888844AGTR1c.729G>T (p.Met243Ile)
c.816G>T (p.Met272Ile)
c.834G>T (p.Met278Ile)
 ClinVar gnomAD v4
3g.148741765G>ACA354888846AGTR1c.730G>A (p.Ala244Thr)
c.817G>A (p.Ala273Thr)
c.835G>A (p.Ala279Thr)
 COSMIC
3g.148741765G>CCA354888847AGTR1c.730G>C (p.Ala244Pro)
c.817G>C (p.Ala273Pro)
c.835G>C (p.Ala279Pro)
3g.148741765G=CA1409910129AGTR1c.730G= (p.Ala244=)
c.817G= (p.Ala273=)
c.835G= (p.Ala279=)
3g.148741765G>TCA2657375AGTR1c.730G>T (p.Ala244Ser)
c.817G>T (p.Ala273Ser)
c.835G>T (p.Ala279Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741766C>ACA354888848AGTR1c.731C>A (p.Ala244Glu)
c.818C>A (p.Ala273Glu)
c.836C>A (p.Ala279Glu)
 dbSNP gnomAD v4
3g.148741766C=CA1409910134AGTR1c.731C= (p.Ala244=)
c.818C= (p.Ala273=)
c.836C= (p.Ala279=)
3g.148741766C>GCA354888849AGTR1c.731C>G (p.Ala244Gly)
c.818C>G (p.Ala273Gly)
c.836C>G (p.Ala279Gly)
3g.148741766C>TCA354888851AGTR1c.731C>T (p.Ala244Val)
c.818C>T (p.Ala273Val)
c.836C>T (p.Ala279Val)
3g.148741767A>CCA436389553AGTR1c.732A>C (p.Ala244=)
c.819A>C (p.Ala273=)
c.837A>C (p.Ala279=)
3g.148741767A>GCA436389556AGTR1c.732A>G (p.Ala244=)
c.819A>G (p.Ala273=)
c.837A>G (p.Ala279=)
 ClinVar
3g.148741767A>TCA436389558AGTR1c.732A>T (p.Ala244=)
c.819A>T (p.Ala273=)
c.837A>T (p.Ala279=)
3g.148741768A=CA1409910137AGTR1c.733A= (p.Ile245=)
c.820A= (p.Ile274=)
c.838A= (p.Ile280=)
3g.148741768A>CCA354888853AGTR1c.733A>C (p.Ile245Leu)
c.820A>C (p.Ile274Leu)
c.838A>C (p.Ile280Leu)
3g.148741768A>GCA2657376AGTR1c.733A>G (p.Ile245Val)
c.820A>G (p.Ile274Val)
c.838A>G (p.Ile280Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741768A>TCA354888855AGTR1c.733A>T (p.Ile245Phe)
c.820A>T (p.Ile274Phe)
c.838A>T (p.Ile280Phe)
3g.148741769T>ACA354888858AGTR1c.734T>A (p.Ile245Asn)
c.821T>A (p.Ile274Asn)
c.839T>A (p.Ile280Asn)
3g.148741769T>CCA2657377AGTR1c.734T>C (p.Ile245Thr)
c.821T>C (p.Ile274Thr)
c.839T>C (p.Ile280Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741769T>GCA354888861AGTR1c.734T>G (p.Ile245Ser)
c.821T>G (p.Ile274Ser)
c.839T>G (p.Ile280Ser)
3g.148741769T=CA1409910141AGTR1c.734T= (p.Ile245=)
c.821T= (p.Ile274=)
c.839T= (p.Ile280=)
3g.148741770T>ACA436389561AGTR1c.735T>A (p.Ile245=)
c.822T>A (p.Ile274=)
c.840T>A (p.Ile280=)
3g.148741770T>CCA436389563AGTR1c.735T>C (p.Ile245=)
c.822T>C (p.Ile274=)
c.840T>C (p.Ile280=)
3g.148741770T>GCA354888862AGTR1c.735T>G (p.Ile245Met)
c.822T>G (p.Ile274Met)
c.840T>G (p.Ile280Met)
3g.148741771G>ACA354888863AGTR1c.736G>A (p.Val246Met)
c.823G>A (p.Val275Met)
c.841G>A (p.Val281Met)
3g.148741771G>CCA2657378AGTR1c.736G>C (p.Val246Leu)
c.823G>C (p.Val275Leu)
c.841G>C (p.Val281Leu)
 ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
3g.148741771G=CA1409910144AGTR1c.736G= (p.Val246=)
c.823G= (p.Val275=)
c.841G= (p.Val281=)
3g.148741771G>TCA354888865AGTR1c.736G>T (p.Val246Leu)
c.823G>T (p.Val275Leu)
c.841G>T (p.Val281Leu)
 gnomAD v4
3g.148741772T>ACA354888868AGTR1c.737T>A (p.Val246Glu)
c.824T>A (p.Val275Glu)
c.842T>A (p.Val281Glu)
3g.148741772T>CCA354888871AGTR1c.737T>C (p.Val246Ala)
c.824T>C (p.Val275Ala)
c.842T>C (p.Val281Ala)
 gnomAD v4
3g.148741772T>GCA354888869AGTR1c.737T>G (p.Val246Gly)
c.824T>G (p.Val275Gly)
c.842T>G (p.Val281Gly)
 gnomAD v4
3g.148741773G>ACA436389568AGTR1c.738G>A (p.Val246=)
c.825G>A (p.Val275=)
c.843G>A (p.Val281=)
 COSMIC
3g.148741773G>CCA436389569AGTR1c.738G>C (p.Val246=)
c.825G>C (p.Val275=)
c.843G>C (p.Val281=)
3g.148741773G>TCA436389570AGTR1c.738G>T (p.Val246=)
c.825G>T (p.Val275=)
c.843G>T (p.Val281=)
3g.148741774C>ACA354888873AGTR1c.739C>A (p.Leu247Ile)
c.826C>A (p.Leu276Ile)
c.844C>A (p.Leu282Ile)
 dbSNP gnomAD v4 COSMIC
3g.148741774C=CA1409910149AGTR1c.739C= (p.Leu247=)
c.826C= (p.Leu276=)
c.844C= (p.Leu282=)
3g.148741774C>GCA354888874AGTR1c.739C>G (p.Leu247Val)
c.826C>G (p.Leu276Val)
c.844C>G (p.Leu282Val)
3g.148741774C>TCA354888875AGTR1c.739C>T (p.Leu247Phe)
c.826C>T (p.Leu276Phe)
c.844C>T (p.Leu282Phe)
 gnomAD v4 COSMIC
3g.148741774_148741776delinsCTTCA1409910148AGTR1c.739_741delinsCTT (p.Leu247=)
c.826_828delinsCTT (p.Leu276=)
c.844_846delinsCTT (p.Leu282=)
3g.148741775T>ACA354888877AGTR1c.740T>A (p.Leu247His)
c.827T>A (p.Leu276His)
c.845T>A (p.Leu282His)
3g.148741775T>CCA354888882AGTR1c.740T>C (p.Leu247Pro)
c.827T>C (p.Leu276Pro)
c.845T>C (p.Leu282Pro)
 COSMIC
3g.148741775T>GCA354888884AGTR1c.740T>G (p.Leu247Arg)
c.827T>G (p.Leu276Arg)
c.845T>G (p.Leu282Arg)
3g.148741777_148741778delCA2657379AGTR1c.742_743del (p.Phe248LeufsTer25)
c.829_830del (p.Phe277LeufsTer25)
c.847_848del (p.Phe283LeufsTer25)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741776T>ACA436389576AGTR1c.741T>A (p.Leu247=)
c.828T>A (p.Leu276=)
c.846T>A (p.Leu282=)
 ClinVar
3g.148741776T>CCA436389574AGTR1c.741T>C (p.Leu247=)
c.828T>C (p.Leu276=)
c.846T>C (p.Leu282=)
3g.148741776T>GCA436389573AGTR1c.741T>G (p.Leu247=)
c.828T>G (p.Leu276=)
c.846T>G (p.Leu282=)
3g.148741777T>ACA354888886AGTR1c.742T>A (p.Phe248Ile)
c.829T>A (p.Phe277Ile)
c.847T>A (p.Phe283Ile)
3g.148741777T>CCA2657380AGTR1c.742T>C (p.Phe248Leu)
c.829T>C (p.Phe277Leu)
c.847T>C (p.Phe283Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741777T>GCA354888891AGTR1c.742T>G (p.Phe248Val)
c.829T>G (p.Phe277Val)
c.847T>G (p.Phe283Val)
3g.148741777T=CA1409910155AGTR1c.742T= (p.Phe248=)
c.829T= (p.Phe277=)
c.847T= (p.Phe283=)
3g.148741778T>ACA354888894AGTR1c.743T>A (p.Phe248Tyr)
c.830T>A (p.Phe277Tyr)
c.848T>A (p.Phe283Tyr)
3g.148741778T>CCA354888893AGTR1c.743T>C (p.Phe248Ser)
c.830T>C (p.Phe277Ser)
c.848T>C (p.Phe283Ser)
3g.148741778T>GCA2657381AGTR1c.743T>G (p.Phe248Cys)
c.830T>G (p.Phe277Cys)
c.848T>G (p.Phe283Cys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741778T=CA1409910158AGTR1c.743T= (p.Phe248=)
c.830T= (p.Phe277=)
c.848T= (p.Phe283=)
3g.148741779C>ACA354888897AGTR1c.744C>A (p.Phe248Leu)
c.831C>A (p.Phe277Leu)
c.849C>A (p.Phe283Leu)
3g.148741779C>GCA354888898AGTR1c.744C>G (p.Phe248Leu)
c.831C>G (p.Phe277Leu)
c.849C>G (p.Phe283Leu)
 gnomAD v4
3g.148741779C>TCA436389577AGTR1c.744C>T (p.Phe248=)
c.831C>T (p.Phe277=)
c.849C>T (p.Phe283=)
3g.148741779_148741781delinsCTTCA1409910160AGTR1c.744_746delinsCTT (p.Phe248=)
c.831_833delinsCTT (p.Phe277=)
c.849_851delinsCTT (p.Phe283=)
3g.148741780T>ACA354888899AGTR1c.745T>A (p.Phe249Ile)
c.832T>A (p.Phe278Ile)
c.850T>A (p.Phe284Ile)
3g.148741780T>CCA354888900AGTR1c.745T>C (p.Phe249Leu)
c.832T>C (p.Phe278Leu)
c.850T>C (p.Phe284Leu)
 gnomAD v4
3g.148741780T>GCA354888901AGTR1c.745T>G (p.Phe249Val)
c.832T>G (p.Phe278Val)
c.850T>G (p.Phe284Val)
3g.148741783_148741784dupCA2668116564AGTR1c.748_749dup (p.Phe251SerfsTer16)
c.835_836dup (p.Phe280SerfsTer16)
c.853_854dup (p.Phe286SerfsTer16)
 gnomAD v4
3g.148741783_148741784delCA2657382AGTR1c.748_749del (p.Phe250LeufsTer23)
c.835_836del (p.Phe279LeufsTer23)
c.853_854del (p.Phe285LeufsTer23)
 dbSNP ExAC gnomAD v2
3g.148741781T>ACA354888902AGTR1c.746T>A (p.Phe249Tyr)
c.833T>A (p.Phe278Tyr)
c.851T>A (p.Phe284Tyr)
3g.148741781T>CCA354888905AGTR1c.746T>C (p.Phe249Ser)
c.833T>C (p.Phe278Ser)
c.851T>C (p.Phe284Ser)
3g.148741781T>GCA354888907AGTR1c.746T>G (p.Phe249Cys)
c.833T>G (p.Phe278Cys)
c.851T>G (p.Phe284Cys)
3g.148741782T>ACA354888913AGTR1c.747T>A (p.Phe249Leu)
c.834T>A (p.Phe278Leu)
c.852T>A (p.Phe284Leu)
3g.148741782T>CCA436389580AGTR1c.747T>C (p.Phe249=)
c.834T>C (p.Phe278=)
c.852T>C (p.Phe284=)
3g.148741782T>GCA354888915AGTR1c.747T>G (p.Phe249Leu)
c.834T>G (p.Phe278Leu)
c.852T>G (p.Phe284Leu)
3g.148741783T>ACA354888918AGTR1c.748T>A (p.Phe250Ile)
c.835T>A (p.Phe279Ile)
c.853T>A (p.Phe285Ile)
3g.148741783T>CCA354888919AGTR1c.748T>C (p.Phe250Leu)
c.835T>C (p.Phe279Leu)
c.853T>C (p.Phe285Leu)
3g.148741783T>GCA354888917AGTR1c.748T>G (p.Phe250Val)
c.835T>G (p.Phe279Val)
c.853T>G (p.Phe285Val)
3g.148741784T>ACA354888921AGTR1c.749T>A (p.Phe250Tyr)
c.836T>A (p.Phe279Tyr)
c.854T>A (p.Phe285Tyr)
3g.148741784T>CCA354888923AGTR1c.749T>C (p.Phe250Ser)
c.836T>C (p.Phe279Ser)
c.854T>C (p.Phe285Ser)
3g.148741784T>GCA354888929AGTR1c.749T>G (p.Phe250Cys)
c.836T>G (p.Phe279Cys)
c.854T>G (p.Phe285Cys)
3g.148741785C>ACA354888932AGTR1c.750C>A (p.Phe250Leu)
c.837C>A (p.Phe279Leu)
c.855C>A (p.Phe285Leu)
3g.148741785C>GCA354888934AGTR1c.750C>G (p.Phe250Leu)
c.837C>G (p.Phe279Leu)
c.855C>G (p.Phe285Leu)
 COSMIC
3g.148741785C>TCA436389584AGTR1c.750C>T (p.Phe250=)
c.837C>T (p.Phe279=)
c.855C>T (p.Phe285=)
 COSMIC
3g.148741786T>ACA354888938AGTR1c.751T>A (p.Phe251Ile)
c.838T>A (p.Phe280Ile)
c.856T>A (p.Phe286Ile)
3g.148741786T>CCA354888935AGTR1c.751T>C (p.Phe251Leu)
c.838T>C (p.Phe280Leu)
c.856T>C (p.Phe286Leu)
3g.148741786T>GCA354888937AGTR1c.751T>G (p.Phe251Val)
c.838T>G (p.Phe280Val)
c.856T>G (p.Phe286Val)
3g.148741787T>ACA354888940AGTR1c.752T>A (p.Phe251Tyr)
c.839T>A (p.Phe280Tyr)
c.857T>A (p.Phe286Tyr)
3g.148741787T>CCA354888942AGTR1c.752T>C (p.Phe251Ser)
c.839T>C (p.Phe280Ser)
c.857T>C (p.Phe286Ser)
3g.148741787T>GCA354888943AGTR1c.752T>G (p.Phe251Cys)
c.839T>G (p.Phe280Cys)
c.857T>G (p.Phe286Cys)
3g.148741788T>ACA354888944AGTR1c.753T>A (p.Phe251Leu)
c.840T>A (p.Phe280Leu)
c.858T>A (p.Phe286Leu)
 COSMIC
3g.148741788T>CCA436389588AGTR1c.753T>C (p.Phe251=)
c.840T>C (p.Phe280=)
c.858T>C (p.Phe286=)
3g.148741788T>GCA354888945AGTR1c.753T>G (p.Phe251Leu)
c.840T>G (p.Phe280Leu)
c.858T>G (p.Phe286Leu)
3g.148741789T>ACA354888950AGTR1c.754T>A (p.Ser252Thr)
c.841T>A (p.Ser281Thr)
c.859T>A (p.Ser287Thr)
3g.148741789T>CCA354888956AGTR1c.754T>C (p.Ser252Pro)
c.841T>C (p.Ser281Pro)
c.859T>C (p.Ser287Pro)
3g.148741789T>GCA354888952AGTR1c.754T>G (p.Ser252Ala)
c.841T>G (p.Ser281Ala)
c.859T>G (p.Ser287Ala)
3g.148741790C>ACA354888960AGTR1c.755C>A (p.Ser252Tyr)
c.842C>A (p.Ser281Tyr)
c.860C>A (p.Ser287Tyr)
3g.148741790C=CA1409910164AGTR1c.755C= (p.Ser252=)
c.842C= (p.Ser281=)
c.860C= (p.Ser287=)
3g.148741790C>GCA354888961AGTR1c.755C>G (p.Ser252Cys)
c.842C>G (p.Ser281Cys)
c.860C>G (p.Ser287Cys)
3g.148741790C>TCA354888964AGTR1c.755C>T (p.Ser252Phe)
c.842C>T (p.Ser281Phe)
c.860C>T (p.Ser287Phe)
 dbSNP gnomAD v2 gnomAD v4
3g.148741791C>ACA436389589AGTR1c.756C>A (p.Ser252=)
c.843C>A (p.Ser281=)
c.861C>A (p.Ser287=)
3g.148741791C>GCA436389590AGTR1c.756C>G (p.Ser252=)
c.843C>G (p.Ser281=)
c.861C>G (p.Ser287=)
3g.148741791C>TCA436389592AGTR1c.756C>T (p.Ser252=)
c.843C>T (p.Ser281=)
c.861C>T (p.Ser287=)
3g.148741792T>ACA354888969AGTR1c.757T>A (p.Trp253Arg)
c.844T>A (p.Trp282Arg)
c.862T>A (p.Trp288Arg)
 gnomAD v4
3g.148741792T>CCA354888971AGTR1c.757T>C (p.Trp253Arg)
c.844T>C (p.Trp282Arg)
c.862T>C (p.Trp288Arg)
3g.148741792T>GCA354888977AGTR1c.757T>G (p.Trp253Gly)
c.844T>G (p.Trp282Gly)
c.862T>G (p.Trp288Gly)
3g.148741793G>ACA354888982AGTR1c.758G>A (p.Trp253Ter)
c.845G>A (p.Trp282Ter)
c.863G>A (p.Trp288Ter)
3g.148741793G>CCA354888983AGTR1c.758G>C (p.Trp253Ser)
c.845G>C (p.Trp282Ser)
c.863G>C (p.Trp288Ser)
3g.148741793G>TCA354888984AGTR1c.758G>T (p.Trp253Leu)
c.845G>T (p.Trp282Leu)
c.863G>T (p.Trp288Leu)
3g.148741794G>ACA354888985AGTR1c.759G>A (p.Trp253Ter)
c.846G>A (p.Trp282Ter)
c.864G>A (p.Trp288Ter)
 COSMIC
3g.148741794G>CCA354888986AGTR1c.759G>C (p.Trp253Cys)
c.846G>C (p.Trp282Cys)
c.864G>C (p.Trp288Cys)
3g.148741794G>TCA354888988AGTR1c.759G>T (p.Trp253Cys)
c.846G>T (p.Trp282Cys)
c.864G>T (p.Trp288Cys)
3g.148741795A>CCA354888991AGTR1c.760A>C (p.Ile254Leu)
c.847A>C (p.Ile283Leu)
c.865A>C (p.Ile289Leu)
3g.148741795A>GCA354888995AGTR1c.760A>G (p.Ile254Val)
c.847A>G (p.Ile283Val)
c.865A>G (p.Ile289Val)
3g.148741795A>TCA354888989AGTR1c.760A>T (p.Ile254Phe)
c.847A>T (p.Ile283Phe)
c.865A>T (p.Ile289Phe)
3g.148741796T>ACA354889000AGTR1c.761T>A (p.Ile254Asn)
c.848T>A (p.Ile283Asn)
c.866T>A (p.Ile289Asn)
 ClinVar dbSNP
3g.148741796T>CCA354888998AGTR1c.761T>C (p.Ile254Thr)
c.848T>C (p.Ile283Thr)
c.866T>C (p.Ile289Thr)
3g.148741796T>GCA354889001AGTR1c.761T>G (p.Ile254Ser)
c.848T>G (p.Ile283Ser)
c.866T>G (p.Ile289Ser)
3g.148741797T>ACA436389594AGTR1c.762T>A (p.Ile254=)
c.849T>A (p.Ile283=)
c.867T>A (p.Ile289=)
3g.148741797T>CCA436389595AGTR1c.762T>C (p.Ile254=)
c.849T>C (p.Ile283=)
c.867T>C (p.Ile289=)
3g.148741797T>GCA354889003AGTR1c.762T>G (p.Ile254Met)
c.849T>G (p.Ile283Met)
c.867T>G (p.Ile289Met)
3g.148741798C>ACA354889014AGTR1c.763C>A (p.Pro255Thr)
c.850C>A (p.Pro284Thr)
c.868C>A (p.Pro290Thr)
 gnomAD v4
3g.148741798C>GCA354889006AGTR1c.763C>G (p.Pro255Ala)
c.850C>G (p.Pro284Ala)
c.868C>G (p.Pro290Ala)
3g.148741798C>TCA354889008AGTR1c.763C>T (p.Pro255Ser)
c.850C>T (p.Pro284Ser)
c.868C>T (p.Pro290Ser)
 gnomAD v4
3g.148741799C>ACA354889016AGTR1c.764C>A (p.Pro255His)
c.851C>A (p.Pro284His)
c.869C>A (p.Pro290His)
3g.148741799C=CA1409910170AGTR1c.764C= (p.Pro255=)
c.851C= (p.Pro284=)
c.869C= (p.Pro290=)
3g.148741799C>GCA354889018AGTR1c.764C>G (p.Pro255Arg)
c.851C>G (p.Pro284Arg)
c.869C>G (p.Pro290Arg)
3g.148741799C>TCA10617600AGTR1c.764C>T (p.Pro255Leu)
c.851C>T (p.Pro284Leu)
c.869C>T (p.Pro290Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.148741800C>ACA2657383AGTR1c.765C>A (p.Pro255=)
c.852C>A (p.Pro284=)
c.870C>A (p.Pro290=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741800C=CA1409910176AGTR1c.765C= (p.Pro255=)
c.852C= (p.Pro284=)
c.870C= (p.Pro290=)
3g.148741800C>GCA436389598AGTR1c.765C>G (p.Pro255=)
c.852C>G (p.Pro284=)
c.870C>G (p.Pro290=)
3g.148741800C>TCA436389600AGTR1c.765C>T (p.Pro255=)
c.852C>T (p.Pro284=)
c.870C>T (p.Pro290=)
3g.148741801C>ACA2657384AGTR1c.766C>A (p.His256Asn)
c.853C>A (p.His285Asn)
c.871C>A (p.His291Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
3g.148741801C=CA1409910178AGTR1c.766C= (p.His256=)
c.853C= (p.His285=)
c.871C= (p.His291=)
3g.148741801C>GCA354889024AGTR1c.766C>G (p.His256Asp)
c.853C>G (p.His285Asp)
c.871C>G (p.His291Asp)
3g.148741801C>TCA354889025AGTR1c.766C>T (p.His256Tyr)
c.853C>T (p.His285Tyr)
c.871C>T (p.His291Tyr)
3g.148741802A>CCA354889026AGTR1c.767A>C (p.His256Pro)
c.854A>C (p.His285Pro)
c.872A>C (p.His291Pro)
3g.148741802A>GCA354889027AGTR1c.767A>G (p.His256Arg)
c.854A>G (p.His285Arg)
c.872A>G (p.His291Arg)
3g.148741802A>TCA354889029AGTR1c.767A>T (p.His256Leu)
c.854A>T (p.His285Leu)
c.872A>T (p.His291Leu)
3g.148741803C>ACA354889031AGTR1c.768C>A (p.His256Gln)
c.855C>A (p.His285Gln)
c.873C>A (p.His291Gln)
 gnomAD v4
3g.148741803C=CA1409910179AGTR1c.768C= (p.His256=)
c.855C= (p.His285=)
c.873C= (p.His291=)
3g.148741803C>GCA354889032AGTR1c.768C>G (p.His256Gln)
c.855C>G (p.His285Gln)
c.873C>G (p.His291Gln)
 gnomAD v4
3g.148741803C>TCA436389601AGTR1c.768C>T (p.His256=)
c.855C>T (p.His285=)
c.873C>T (p.His291=)
 dbSNP gnomAD v3 gnomAD v4
3g.148741804C>ACA354889034AGTR1c.769C>A (p.Gln257Lys)
c.856C>A (p.Gln286Lys)
c.874C>A (p.Gln292Lys)
 gnomAD v4
3g.148741804C=CA1409910182AGTR1c.769C= (p.Gln257=)
c.856C= (p.Gln286=)
c.874C= (p.Gln292=)
3g.148741804C>GCA354889035AGTR1c.769C>G (p.Gln257Glu)
c.856C>G (p.Gln286Glu)
c.874C>G (p.Gln292Glu)
 gnomAD v4
3g.148741804C>TCA2657385AGTR1c.769C>T (p.Gln257Ter)
c.856C>T (p.Gln286Ter)
c.874C>T (p.Gln292Ter)
 dbSNP ExAC gnomAD v2
3g.148741805A>CCA354889036AGTR1c.770A>C (p.Gln257Pro)
c.857A>C (p.Gln286Pro)
c.875A>C (p.Gln292Pro)
3g.148741805A>GCA354889038AGTR1c.770A>G (p.Gln257Arg)
c.857A>G (p.Gln286Arg)
c.875A>G (p.Gln292Arg)
3g.148741805A>TCA354889040AGTR1c.770A>T (p.Gln257Leu)
c.857A>T (p.Gln286Leu)
c.875A>T (p.Gln292Leu)
3g.148741806A>CCA354889041AGTR1c.771A>C (p.Gln257His)
c.858A>C (p.Gln286His)
c.876A>C (p.Gln292His)
3g.148741806A>GCA436389603AGTR1c.771A>G (p.Gln257=)
c.858A>G (p.Gln286=)
c.876A>G (p.Gln292=)
3g.148741806A>TCA354889043AGTR1c.771A>T (p.Gln257His)
c.858A>T (p.Gln286His)
c.876A>T (p.Gln292His)
3g.148741807A>CCA354889044AGTR1c.772A>C (p.Ile258Leu)
c.859A>C (p.Ile287Leu)
c.877A>C (p.Ile293Leu)
3g.148741807A>GCA354889046AGTR1c.772A>G (p.Ile258Val)
c.859A>G (p.Ile287Val)
c.877A>G (p.Ile293Val)
3g.148741807A>TCA354889047AGTR1c.772A>T (p.Ile258Leu)
c.859A>T (p.Ile287Leu)
c.877A>T (p.Ile293Leu)
3g.148741809_148741810delCA2668116565AGTR1c.774_775del (p.Phe259HisfsTer14)
c.861_862del (p.Phe288HisfsTer14)
c.879_880del (p.Phe294HisfsTer14)
 gnomAD v4
3g.148741808T>ACA354889056AGTR1c.773T>A (p.Ile258Lys)
c.860T>A (p.Ile287Lys)
c.878T>A (p.Ile293Lys)
3g.148741808T>CCA2657386AGTR1c.773T>C (p.Ile258Thr)
c.860T>C (p.Ile287Thr)
c.878T>C (p.Ile293Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741808T>GCA354889051AGTR1c.773T>G (p.Ile258Arg)
c.860T>G (p.Ile287Arg)
c.878T>G (p.Ile293Arg)
3g.148741808T=CA1409910184AGTR1c.773T= (p.Ile258=)
c.860T= (p.Ile287=)
c.878T= (p.Ile293=)
3g.148741809A=CA1409910187AGTR1c.774A= (p.Ile258=)
c.861A= (p.Ile287=)
c.879A= (p.Ile293=)
3g.148741809A>CCA436389606AGTR1c.774A>C (p.Ile258=)
c.861A>C (p.Ile287=)
c.879A>C (p.Ile293=)
3g.148741809A>GCA354889058AGTR1c.774A>G (p.Ile258Met)
c.861A>G (p.Ile287Met)
c.879A>G (p.Ile293Met)
 dbSNP gnomAD v2 gnomAD v4
3g.148741809A>TCA436389605AGTR1c.774A>T (p.Ile258=)
c.861A>T (p.Ile287=)
c.879A>T (p.Ile293=)
3g.148741810T>ACA354889059AGTR1c.775T>A (p.Phe259Ile)
c.862T>A (p.Phe288Ile)
c.880T>A (p.Phe294Ile)
3g.148741810T>CCA354889060AGTR1c.775T>C (p.Phe259Leu)
c.862T>C (p.Phe288Leu)
c.880T>C (p.Phe294Leu)
3g.148741810T>GCA354889061AGTR1c.775T>G (p.Phe259Val)
c.862T>G (p.Phe288Val)
c.880T>G (p.Phe294Val)
3g.148741811T>ACA354889063AGTR1c.776T>A (p.Phe259Tyr)
c.863T>A (p.Phe288Tyr)
c.881T>A (p.Phe294Tyr)
3g.148741811T>CCA354889065AGTR1c.776T>C (p.Phe259Ser)
c.863T>C (p.Phe288Ser)
c.881T>C (p.Phe294Ser)
3g.148741811T>GCA354889067AGTR1c.776T>G (p.Phe259Cys)
c.863T>G (p.Phe288Cys)
c.881T>G (p.Phe294Cys)
3g.148741812C>ACA354889068AGTR1c.777C>A (p.Phe259Leu)
c.864C>A (p.Phe288Leu)
c.882C>A (p.Phe294Leu)
3g.148741812C>GCA354889069AGTR1c.777C>G (p.Phe259Leu)
c.864C>G (p.Phe288Leu)
c.882C>G (p.Phe294Leu)
3g.148741812C>TCA436389608AGTR1c.777C>T (p.Phe259=)
c.864C>T (p.Phe288=)
c.882C>T (p.Phe294=)
3g.148741813A>CCA354889070AGTR1c.778A>C (p.Thr260Pro)
c.865A>C (p.Thr289Pro)
c.883A>C (p.Thr295Pro)
3g.148741813A>GCA354889071AGTR1c.778A>G (p.Thr260Ala)
c.865A>G (p.Thr289Ala)
c.883A>G (p.Thr295Ala)
 COSMIC
3g.148741813A>TCA354889073AGTR1c.778A>T (p.Thr260Ser)
c.865A>T (p.Thr289Ser)
c.883A>T (p.Thr295Ser)
3g.148741814C>ACA354889077AGTR1c.779C>A (p.Thr260Asn)
c.866C>A (p.Thr289Asn)
c.884C>A (p.Thr295Asn)
3g.148741814C=CA1409910190AGTR1c.779C= (p.Thr260=)
c.866C= (p.Thr289=)
c.884C= (p.Thr295=)
3g.148741814C>GCA354889079AGTR1c.779C>G (p.Thr260Ser)
c.866C>G (p.Thr289Ser)
c.884C>G (p.Thr295Ser)
3g.148741814C>TCA2657387AGTR1c.779C>T (p.Thr260Ile)
c.866C>T (p.Thr289Ile)
c.884C>T (p.Thr295Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741815T>ACA436389610AGTR1c.780T>A (p.Thr260=)
c.867T>A (p.Thr289=)
c.885T>A (p.Thr295=)
3g.148741815T>CCA436389612AGTR1c.780T>C (p.Thr260=)
c.867T>C (p.Thr289=)
c.885T>C (p.Thr295=)
3g.148741815T>GCA436389611AGTR1c.780T>G (p.Thr260=)
c.867T>G (p.Thr289=)
c.885T>G (p.Thr295=)
3g.148741816T>ACA354889082AGTR1c.781T>A (p.Phe261Ile)
c.868T>A (p.Phe290Ile)
c.886T>A (p.Phe296Ile)
3g.148741816T>CCA354889084AGTR1c.781T>C (p.Phe261Leu)
c.868T>C (p.Phe290Leu)
c.886T>C (p.Phe296Leu)
3g.148741816T>GCA354889085AGTR1c.781T>G (p.Phe261Val)
c.868T>G (p.Phe290Val)
c.886T>G (p.Phe296Val)
3g.148741817T>ACA354889087AGTR1c.782T>A (p.Phe261Tyr)
c.869T>A (p.Phe290Tyr)
c.887T>A (p.Phe296Tyr)
3g.148741817T>CCA354889089AGTR1c.782T>C (p.Phe261Ser)
c.869T>C (p.Phe290Ser)
c.887T>C (p.Phe296Ser)
3g.148741817T>GCA354889090AGTR1c.782T>G (p.Phe261Cys)
c.869T>G (p.Phe290Cys)
c.887T>G (p.Phe296Cys)
3g.148741818T>ACA354889092AGTR1c.783T>A (p.Phe261Leu)
c.870T>A (p.Phe290Leu)
c.888T>A (p.Phe296Leu)
3g.148741818T>CCA436389616AGTR1c.783T>C (p.Phe261=)
c.870T>C (p.Phe290=)
c.888T>C (p.Phe296=)
 dbSNP gnomAD v4
3g.148741818T>GCA354889093AGTR1c.783T>G (p.Phe261Leu)
c.870T>G (p.Phe290Leu)
c.888T>G (p.Phe296Leu)
3g.148741818T=CA1409910193AGTR1c.783T= (p.Phe261=)
c.870T= (p.Phe290=)
c.888T= (p.Phe296=)
3g.148741819C>ACA354889095AGTR1c.784C>A (p.Leu262Met)
c.871C>A (p.Leu291Met)
c.889C>A (p.Leu297Met)
 dbSNP COSMIC
3g.148741819C=CA1409910196AGTR1c.784C= (p.Leu262=)
c.871C= (p.Leu291=)
c.889C= (p.Leu297=)
3g.148741819C>GCA354889096AGTR1c.784C>G (p.Leu262Val)
c.871C>G (p.Leu291Val)
c.889C>G (p.Leu297Val)
 dbSNP gnomAD v4
3g.148741819C>TCA436389617AGTR1c.784C>T (p.Leu262=)
c.871C>T (p.Leu291=)
c.889C>T (p.Leu297=)
3g.148741820T>ACA354889098AGTR1c.785T>A (p.Leu262Gln)
c.872T>A (p.Leu291Gln)
c.890T>A (p.Leu297Gln)
 dbSNP gnomAD v3 gnomAD v4
3g.148741820T>CCA354889099AGTR1c.785T>C (p.Leu262Pro)
c.872T>C (p.Leu291Pro)
c.890T>C (p.Leu297Pro)
3g.148741820T>GCA354889100AGTR1c.785T>G (p.Leu262Arg)
c.872T>G (p.Leu291Arg)
c.890T>G (p.Leu297Arg)
3g.148741820T=CA1409910198AGTR1c.785T= (p.Leu262=)
c.872T= (p.Leu291=)
c.890T= (p.Leu297=)
3g.148741821G>ACA436389618AGTR1c.786G>A (p.Leu262=)
c.873G>A (p.Leu291=)
c.891G>A (p.Leu297=)
3g.148741821G>CCA436389619AGTR1c.786G>C (p.Leu262=)
c.873G>C (p.Leu291=)
c.891G>C (p.Leu297=)
3g.148741821G=CA1409910200AGTR1c.786G= (p.Leu262=)
c.873G= (p.Leu291=)
c.891G= (p.Leu297=)
3g.148741821G>TCA436389620AGTR1c.786G>T (p.Leu262=)
c.873G>T (p.Leu291=)
c.891G>T (p.Leu297=)
 dbSNP
3g.148741822G>ACA354889105AGTR1c.787G>A (p.Asp263Asn)
c.874G>A (p.Asp292Asn)
c.892G>A (p.Asp298Asn)
 COSMIC
3g.148741822G>CCA354889104AGTR1c.787G>C (p.Asp263His)
c.874G>C (p.Asp292His)
c.892G>C (p.Asp298His)
3g.148741822G>TCA354889102AGTR1c.787G>T (p.Asp263Tyr)
c.874G>T (p.Asp292Tyr)
c.892G>T (p.Asp298Tyr)
 gnomAD v4
3g.148741823A=CA1409910202AGTR1c.788A= (p.Asp263=)
c.875A= (p.Asp292=)
c.893A= (p.Asp298=)
3g.148741823A>CCA354889107AGTR1c.788A>C (p.Asp263Ala)
c.875A>C (p.Asp292Ala)
c.893A>C (p.Asp298Ala)
3g.148741823A>GCA2657388AGTR1c.788A>G (p.Asp263Gly)
c.875A>G (p.Asp292Gly)
c.893A>G (p.Asp298Gly)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.148741823A>TCA354889109AGTR1c.788A>T (p.Asp263Val)
c.875A>T (p.Asp292Val)
c.893A>T (p.Asp298Val)
 gnomAD v4
3g.148741824T>ACA354889112AGTR1c.789T>A (p.Asp263Glu)
c.876T>A (p.Asp292Glu)
c.894T>A (p.Asp298Glu)
3g.148741824T>CCA436389621AGTR1c.789T>C (p.Asp263=)
c.876T>C (p.Asp292=)
c.894T>C (p.Asp298=)
3g.148741824T>GCA354889114AGTR1c.789T>G (p.Asp263Glu)
c.876T>G (p.Asp292Glu)
c.894T>G (p.Asp298Glu)
 gnomAD v4
3g.148741825G>ACA354889116AGTR1c.790G>A (p.Val264Ile)
c.877G>A (p.Val293Ile)
c.895G>A (p.Val299Ile)
3g.148741825G>CCA354889127AGTR1c.790G>C (p.Val264Leu)
c.877G>C (p.Val293Leu)
c.895G>C (p.Val299Leu)
3g.148741825G>TCA354889129AGTR1c.790G>T (p.Val264Leu)
c.877G>T (p.Val293Leu)
c.895G>T (p.Val299Leu)
3g.148741826T>ACA354889131AGTR1c.791T>A (p.Val264Glu)
c.878T>A (p.Val293Glu)
c.896T>A (p.Val299Glu)
3g.148741826T>CCA354889132AGTR1c.791T>C (p.Val264Ala)
c.878T>C (p.Val293Ala)
c.896T>C (p.Val299Ala)
 gnomAD v4
3g.148741826T>GCA354889134AGTR1c.791T>G (p.Val264Gly)
c.878T>G (p.Val293Gly)
c.896T>G (p.Val299Gly)
3g.148741827A=CA1409910203AGTR1c.792A= (p.Val264=)
c.879A= (p.Val293=)
c.897A= (p.Val299=)
3g.148741827A>CCA436389625AGTR1c.792A>C (p.Val264=)
c.879A>C (p.Val293=)
c.897A>C (p.Val299=)
3g.148741827A>GCA2657389AGTR1c.792A>G (p.Val264=)
c.879A>G (p.Val293=)
c.897A>G (p.Val299=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.148741827A>TCA436389626AGTR1c.792A>T (p.Val264=)
c.879A>T (p.Val293=)
c.897A>T (p.Val299=)

Number of alleles fetched