| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.116172482C>A | CA414337815 | AGTR2 | c.202C>A (p.Leu68Met) n.670C>A | |
| X | g.116172482C>G | CA414337816 | AGTR2 | c.202C>G (p.Leu68Val) n.670C>G | |
| X | g.116172482C>T | CA518449223 | AGTR2 | c.202C>T (p.Leu68=) n.670C>T | |
| X | g.116172482_116172483del | CA2694510861 | AGTR2 | c.202_203del (p.Leu68ValfsTer8) n.670_671del | gnomAD v4 |
| X | g.116172483T>A | CA414337819 | AGTR2 | c.203T>A (p.Leu68Gln) n.671T>A | |
| X | g.116172483T>C | CA414337818 | AGTR2 | c.203T>C (p.Leu68Pro) n.671T>C | |
| X | g.116172483T>G | CA414337817 | AGTR2 | c.203T>G (p.Leu68Arg) n.671T>G | |
| X | g.116172484G>A | CA518449224 | AGTR2 | c.204G>A (p.Leu68=) n.672G>A | |
| X | g.116172484G>C | CA518449225 | AGTR2 | c.204G>C (p.Leu68=) n.672G>C | |
| X | g.116172484G>T | CA518449226 | AGTR2 | c.204G>T (p.Leu68=) n.672G>T | |
| X | g.116172485T>A | CA414337820 | AGTR2 | c.205T>A (p.Phe69Ile) n.673T>A | |
| X | g.116172485T>C | CA414337821 | AGTR2 | c.205T>C (p.Phe69Leu) n.673T>C | gnomAD v4 |
| X | g.116172485T>G | CA414337822 | AGTR2 | c.205T>G (p.Phe69Val) n.673T>G | |
| X | g.116172486T>A | CA414337823 | AGTR2 | c.206T>A (p.Phe69Tyr) n.674T>A | |
| X | g.116172486T>C | CA414337824 | AGTR2 | c.206T>C (p.Phe69Ser) n.674T>C | |
| X | g.116172486T>G | CA414337825 | AGTR2 | c.206T>G (p.Phe69Cys) n.674T>G | |
| X | g.116172487T>A | CA414337826 | AGTR2 | c.207T>A (p.Phe69Leu) n.675T>A | |
| X | g.116172487T>C | CA518449227 | AGTR2 | c.207T>C (p.Phe69=) n.675T>C | |
| X | g.116172487T>G | CA414337827 | AGTR2 | c.207T>G (p.Phe69Leu) n.675T>G | |
| X | g.116172488T>A | CA414337828 | AGTR2 | c.208T>A (p.Cys70Ser) n.676T>A | |
| X | g.116172488T>C | CA414337829 | AGTR2 | c.208T>C (p.Cys70Arg) n.676T>C | |
| X | g.116172488T>G | CA414337830 | AGTR2 | c.208T>G (p.Cys70Gly) n.676T>G | |
| X | g.116172488_116172489delinsTG | CA2453331721 | AGTR2 | c.208_209delinsTG (p.Cys70=) n.676_677delinsTG | |
| X | g.116172489del | CA644065609 | AGTR2 | c.209del (p.Cys70PhefsTer?) n.677del | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172489G>A | CA414337832 | AGTR2 | c.209G>A (p.Cys70Tyr) n.677G>A | gnomAD v4 COSMIC |
| X | g.116172489G>C | CA414337833 | AGTR2 | c.209G>C (p.Cys70Ser) n.677G>C | |
| X | g.116172489G>T | CA414337831 | AGTR2 | c.209G>T (p.Cys70Phe) n.677G>T | |
| X | g.116172490T>A | CA414337834 | AGTR2 | c.210T>A (p.Cys70Ter) n.678T>A | |
| X | g.116172490T>C | CA518449228 | AGTR2 | c.210T>C (p.Cys70=) n.678T>C | gnomAD v4 |
| X | g.116172490T>G | CA414337835 | AGTR2 | c.210T>G (p.Cys70Trp) n.678T>G | |
| X | g.116172491T>A | CA10497243 | AGTR2 | c.211T>A (p.Cys71Ser) n.679T>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172491T>C | CA414337836 | AGTR2 | c.211T>C (p.Cys71Arg) n.679T>C | |
| X | g.116172491T>G | CA414337837 | AGTR2 | c.211T>G (p.Cys71Gly) n.679T>G | |
| X | g.116172491T= | CA2453331722 | AGTR2 | c.211T= (p.Cys71=) n.679T= | |
| X | g.116172492G>A | CA414337840 | AGTR2 | c.212G>A (p.Cys71Tyr) n.680G>A | |
| X | g.116172492G>C | CA414337838 | AGTR2 | c.212G>C (p.Cys71Ser) n.680G>C | |
| X | g.116172492G>T | CA414337839 | AGTR2 | c.212G>T (p.Cys71Phe) n.680G>T | |
| X | g.116172493T>A | CA414337841 | AGTR2 | c.213T>A (p.Cys71Ter) n.681T>A | |
| X | g.116172493T>C | CA518449229 | AGTR2 | c.213T>C (p.Cys71=) n.681T>C | |
| X | g.116172493T>G | CA414337842 | AGTR2 | c.213T>G (p.Cys71Trp) n.681T>G | |
| X | g.116172494C>A | CA414337843 | AGTR2 | c.214C>A (p.Gln72Lys) n.682C>A | |
| X | g.116172494C= | CA2453331723 | AGTR2 | c.214C= (p.Gln72=) n.682C= | |
| X | g.116172494C>G | CA10497244 | AGTR2 | c.214C>G (p.Gln72Glu) n.682C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172494C>T | CA414337844 | AGTR2 | c.214C>T (p.Gln72Ter) n.682C>T | |
| X | g.116172495A= | CA2453331724 | AGTR2 | c.215A= (p.Gln72=) n.683A= | |
| X | g.116172495A>C | CA414337845 | AGTR2 | c.215A>C (p.Gln72Pro) n.683A>C | |
| X | g.116172495A>G | CA414337847 | AGTR2 | c.215A>G (p.Gln72Arg) n.683A>G | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172495A>T | CA414337846 | AGTR2 | c.215A>T (p.Gln72Leu) n.683A>T | |
| X | g.116172498dup | CA2501363573 | AGTR2 | c.218dup (p.Pro75SerfsTer2) n.686dup | |
| X | g.116172496A>C | CA414337848 | AGTR2 | c.216A>C (p.Gln72His) n.684A>C | COSMIC |
| X | g.116172496A>G | CA518449294 | AGTR2 | c.216A>G (p.Gln72=) n.684A>G | |
| X | g.116172496A>T | CA414337849 | AGTR2 | c.216A>T (p.Gln72His) n.684A>T | |
| X | g.116172497A>C | CA414337850 | AGTR2 | c.217A>C (p.Lys73Gln) n.685A>C | |
| X | g.116172497A>G | CA414337851 | AGTR2 | c.217A>G (p.Lys73Glu) n.685A>G | |
| X | g.116172497A>T | CA414337852 | AGTR2 | c.217A>T (p.Lys73Ter) n.685A>T | |
| X | g.116172498A>C | CA414337853 | AGTR2 | c.218A>C (p.Lys73Thr) n.686A>C | |
| X | g.116172498A>G | CA414337854 | AGTR2 | c.218A>G (p.Lys73Arg) n.686A>G | |
| X | g.116172498A>T | CA414337855 | AGTR2 | c.218A>T (p.Lys73Met) n.686A>T | |
| X | g.116172499G>A | CA10497245 | AGTR2 | c.219G>A (p.Lys73=) n.687G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172499G>C | CA414337856 | AGTR2 | c.219G>C (p.Lys73Asn) n.687G>C | dbSNP |
| X | g.116172499G= | CA2453331725 | AGTR2 | c.219G= (p.Lys73=) n.687G= | |
| X | g.116172499G>T | CA414337857 | AGTR2 | c.219G>T (p.Lys73Asn) n.687G>T | |
| X | g.116172500G>A | CA414337860 | AGTR2 | c.220G>A (p.Gly74Ser) n.688G>A | COSMIC |
| X | g.116172500G>C | CA414337859 | AGTR2 | c.220G>C (p.Gly74Arg) n.688G>C | dbSNP gnomAD v4 |
| X | g.116172500G= | CA2453331726 | AGTR2 | c.220G= (p.Gly74=) n.688G= | |
| X | g.116172500G>T | CA414337858 | AGTR2 | c.220G>T (p.Gly74Cys) n.688G>T | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172501G>A | CA414337861 | AGTR2 | c.221G>A (p.Gly74Asp) n.689G>A | |
| X | g.116172501G>C | CA414337862 | AGTR2 | c.221G>C (p.Gly74Ala) n.689G>C | |
| X | g.116172501G= | CA2453331727 | AGTR2 | c.221G= (p.Gly74=) n.689G= | |
| X | g.116172501G>T | CA10497246 | AGTR2 | c.221G>T (p.Gly74Val) n.689G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.116172502T>A | CA518449299 | AGTR2 | c.222T>A (p.Gly74=) n.690T>A | |
| X | g.116172502T>C | CA518449301 | AGTR2 | c.222T>C (p.Gly74=) n.690T>C | |
| X | g.116172502T>G | CA518449302 | AGTR2 | c.222T>G (p.Gly74=) n.690T>G | |
| X | g.116172503C>A | CA414337863 | AGTR2 | c.223C>A (p.Pro75Thr) n.691C>A | |
| X | g.116172503C>G | CA414337864 | AGTR2 | c.223C>G (p.Pro75Ala) n.691C>G | |
| X | g.116172503C>T | CA414337865 | AGTR2 | c.223C>T (p.Pro75Ser) n.691C>T | |
| X | g.116172504C>A | CA414337866 | AGTR2 | c.224C>A (p.Pro75His) n.692C>A | |
| X | g.116172504C>G | CA414337867 | AGTR2 | c.224C>G (p.Pro75Arg) n.692C>G | |
| X | g.116172504C>T | CA414337868 | AGTR2 | c.224C>T (p.Pro75Leu) n.692C>T | gnomAD v4 |
| X | g.116172505T>A | CA518449305 | AGTR2 | c.225T>A (p.Pro75=) n.693T>A | gnomAD v4 |
| X | g.116172505T>C | CA518449307 | AGTR2 | c.225T>C (p.Pro75=) n.693T>C | |
| X | g.116172505T>G | CA518449306 | AGTR2 | c.225T>G (p.Pro75=) n.693T>G | |
| X | g.116172506A>C | CA414337869 | AGTR2 | c.226A>C (p.Lys76Gln) n.694A>C | |
| X | g.116172506A>G | CA414337870 | AGTR2 | c.226A>G (p.Lys76Glu) n.694A>G | COSMIC |
| X | g.116172506A>T | CA414337871 | AGTR2 | c.226A>T (p.Lys76Ter) n.694A>T | |
| X | g.116172510del | CA2523096298 | AGTR2 | c.230del (p.Lys77ArgfsTer?) n.698del | |
| X | g.116172507A>C | CA414337872 | AGTR2 | c.227A>C (p.Lys76Thr) n.695A>C | |
| X | g.116172507A>G | CA414337873 | AGTR2 | c.227A>G (p.Lys76Arg) n.695A>G | |
| X | g.116172507A>T | CA414337874 | AGTR2 | c.227A>T (p.Lys76Ile) n.695A>T | |
| X | g.116172508A= | CA2453331728 | AGTR2 | c.228A= (p.Lys76=) n.696A= | |
| X | g.116172508A>C | CA414337876 | AGTR2 | c.228A>C (p.Lys76Asn) n.696A>C | |
| X | g.116172508A>G | CA518449312 | AGTR2 | c.228A>G (p.Lys76=) n.696A>G | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172508A>T | CA414337875 | AGTR2 | c.228A>T (p.Lys76Asn) n.696A>T | |
| X | g.116172509A>C | CA414337877 | AGTR2 | c.229A>C (p.Lys77Gln) n.697A>C | |
| X | g.116172509A>G | CA414337878 | AGTR2 | c.229A>G (p.Lys77Glu) n.697A>G | |
| X | g.116172509A>T | CA414337879 | AGTR2 | c.229A>T (p.Lys77Ter) n.697A>T | |
| X | g.116172510A= | CA2453331729 | AGTR2 | c.230A= (p.Lys77=) n.698A= | |
| X | g.116172510A>C | CA414337880 | AGTR2 | c.230A>C (p.Lys77Thr) n.698A>C | gnomAD v4 |
| X | g.116172510A>G | CA414337881 | AGTR2 | c.230A>G (p.Lys77Arg) n.698A>G | gnomAD v4 |
| X | g.116172510A>T | CA414337882 | AGTR2 | c.230A>T (p.Lys77Met) n.698A>T | |
| X | g.116172510_116172511insAAAGTGAGT | CA644065623 | AGTR2 | c.230_231insAAAGTGAGT (p.Lys78LysfsTer2) n.698_699insAAAGTGAGT | dbSNP gnomAD v2 |
| X | g.116172511G>A | CA518449315 | AGTR2 | c.231G>A (p.Lys77=) n.699G>A | dbSNP COSMIC |
| X | g.116172511G>C | CA414337883 | AGTR2 | c.231G>C (p.Lys77Asn) n.699G>C | |
| X | g.116172511G= | CA2453331730 | AGTR2 | c.231G= (p.Lys77=) n.699G= | |
| X | g.116172511G>T | CA233454 | AGTR2 | c.231G>T (p.Lys77Asn) n.699G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172512G>A | CA414337884 | AGTR2 | c.232G>A (p.Val78Ile) n.700G>A | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172512G>C | CA414337885 | AGTR2 | c.232G>C (p.Val78Leu) n.700G>C | |
| X | g.116172512G= | CA2453331731 | AGTR2 | c.232G= (p.Val78=) n.700G= | |
| X | g.116172512G>T | CA414337886 | AGTR2 | c.232G>T (p.Val78Phe) n.700G>T | |
| X | g.116172513T>A | CA414337889 | AGTR2 | c.233T>A (p.Val78Asp) n.701T>A | |
| X | g.116172513T>C | CA414337888 | AGTR2 | c.233T>C (p.Val78Ala) n.701T>C | COSMIC |
| X | g.116172513T>G | CA414337887 | AGTR2 | c.233T>G (p.Val78Gly) n.701T>G | |
| X | g.116172514T>A | CA518449327 | AGTR2 | c.234T>A (p.Val78=) n.702T>A | |
| X | g.116172514T>C | CA518449324 | AGTR2 | c.234T>C (p.Val78=) n.702T>C | |
| X | g.116172514T>G | CA518449325 | AGTR2 | c.234T>G (p.Val78=) n.702T>G | |
| X | g.116172515T>A | CA414337890 | AGTR2 | c.235T>A (p.Ser79Thr) n.703T>A | |
| X | g.116172515T>C | CA414337891 | AGTR2 | c.235T>C (p.Ser79Pro) n.703T>C | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172515T>G | CA414337892 | AGTR2 | c.235T>G (p.Ser79Ala) n.703T>G | |
| X | g.116172515T= | CA2453331732 | AGTR2 | c.235T= (p.Ser79=) n.703T= | |
| X | g.116172516C>A | CA10497248 | AGTR2 | c.236C>A (p.Ser79Tyr) n.704C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172516C= | CA2453331733 | AGTR2 | c.236C= (p.Ser79=) n.704C= | |
| X | g.116172516C>G | CA10497247 | AGTR2 | c.236C>G (p.Ser79Cys) n.704C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172516C>T | CA414337893 | AGTR2 | c.236C>T (p.Ser79Phe) n.704C>T | |
| X | g.116172517T>A | CA518449332 | AGTR2 | c.237T>A (p.Ser79=) n.705T>A | |
| X | g.116172517T>C | CA518449333 | AGTR2 | c.237T>C (p.Ser79=) n.705T>C | |
| X | g.116172517T>G | CA518449335 | AGTR2 | c.237T>G (p.Ser79=) n.705T>G | |
| X | g.116172518A>C | CA414337894 | AGTR2 | c.238A>C (p.Ser80Arg) n.706A>C | |
| X | g.116172518A>G | CA414337895 | AGTR2 | c.238A>G (p.Ser80Gly) n.706A>G | |
| X | g.116172518A>T | CA414337896 | AGTR2 | c.238A>T (p.Ser80Cys) n.706A>T | |
| X | g.116172519G>A | CA414337897 | AGTR2 | c.239G>A (p.Ser80Asn) n.707G>A | dbSNP gnomAD v3 gnomAD v4 |
| X | g.116172519G>C | CA414337898 | AGTR2 | c.239G>C (p.Ser80Thr) n.707G>C | |
| X | g.116172519G= | CA2453331734 | AGTR2 | c.239G= (p.Ser80=) n.707G= | |
| X | g.116172519G>T | CA414337899 | AGTR2 | c.239G>T (p.Ser80Ile) n.707G>T | dbSNP |
| X | g.116172520C>A | CA334723682 | AGTR2 | c.240C>A (p.Ser80Arg) n.708C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172520C= | CA2453331735 | AGTR2 | c.240C= (p.Ser80=) n.708C= | |
| X | g.116172520C>G | CA414337900 | AGTR2 | c.240C>G (p.Ser80Arg) n.708C>G | |
| X | g.116172520C>T | CA518449337 | AGTR2 | c.240C>T (p.Ser80=) n.708C>T | |
| X | g.116172521A= | CA2453331736 | AGTR2 | c.241A= (p.Ile81=) n.709A= | |
| X | g.116172521A>C | CA414337901 | AGTR2 | c.241A>C (p.Ile81Leu) n.709A>C | |
| X | g.116172521A>G | CA414337902 | AGTR2 | c.241A>G (p.Ile81Val) n.709A>G | |
| X | g.116172521A>T | CA10497249 | AGTR2 | c.241A>T (p.Ile81Leu) n.709A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.116172522T>A | CA414337903 | AGTR2 | c.242T>A (p.Ile81Lys) n.710T>A | |
| X | g.116172522T>C | CA414337904 | AGTR2 | c.242T>C (p.Ile81Thr) n.710T>C | |
| X | g.116172522T>G | CA414337905 | AGTR2 | c.242T>G (p.Ile81Arg) n.710T>G | |
| X | g.116172523A>C | CA518449343 | AGTR2 | c.243A>C (p.Ile81=) n.711A>C | |
| X | g.116172523A>G | CA414337906 | AGTR2 | c.243A>G (p.Ile81Met) n.711A>G | gnomAD v4 |
| X | g.116172523A>T | CA518449345 | AGTR2 | c.243A>T (p.Ile81=) n.711A>T | |
| X | g.116172524T>A | CA334723683 | AGTR2 | c.244T>A (p.Tyr82Asn) n.712T>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172524T>C | CA414337907 | AGTR2 | c.244T>C (p.Tyr82His) n.712T>C | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172524T>G | CA414337908 | AGTR2 | c.244T>G (p.Tyr82Asp) n.712T>G | |
| X | g.116172524T= | CA2453331737 | AGTR2 | c.244T= (p.Tyr82=) n.712T= | |
| X | g.116172525A>C | CA414337909 | AGTR2 | c.245A>C (p.Tyr82Ser) n.713A>C | |
| X | g.116172525A>G | CA414337910 | AGTR2 | c.245A>G (p.Tyr82Cys) n.713A>G | gnomAD v4 |
| X | g.116172525A>T | CA414337911 | AGTR2 | c.245A>T (p.Tyr82Phe) n.713A>T | |
| X | g.116172526C>A | CA414337913 | AGTR2 | c.246C>A (p.Tyr82Ter) n.714C>A | |
| X | g.116172526C>G | CA414337912 | AGTR2 | c.246C>G (p.Tyr82Ter) n.714C>G | gnomAD v4 |
| X | g.116172526C>T | CA518449355 | AGTR2 | c.246C>T (p.Tyr82=) n.714C>T | gnomAD v4 |
| X | g.116172527A= | CA2453331738 | AGTR2 | c.247A= (p.Ile83=) n.715A= | |
| X | g.116172527A>C | CA414337914 | AGTR2 | c.247A>C (p.Ile83Leu) n.715A>C | |
| X | g.116172527A>G | CA414337916 | AGTR2 | c.247A>G (p.Ile83Val) n.715A>G | |
| X | g.116172527A>T | CA414337915 | AGTR2 | c.247A>T (p.Ile83Phe) n.715A>T | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172528T>A | CA414337917 | AGTR2 | c.248T>A (p.Ile83Asn) n.716T>A | COSMIC |
| X | g.116172528T>C | CA414337919 | AGTR2 | c.248T>C (p.Ile83Thr) n.716T>C | |
| X | g.116172528T>G | CA414337918 | AGTR2 | c.248T>G (p.Ile83Ser) n.716T>G | |
| X | g.116172529C>A | CA518449361 | AGTR2 | c.249C>A (p.Ile83=) n.717C>A | |
| X | g.116172529C>G | CA414337920 | AGTR2 | c.249C>G (p.Ile83Met) n.717C>G | |
| X | g.116172529C>T | CA518449362 | AGTR2 | c.249C>T (p.Ile83=) n.717C>T | |
| X | g.116172530T>A | CA414337921 | AGTR2 | c.250T>A (p.Phe84Ile) n.718T>A | |
| X | g.116172530T>C | CA414337922 | AGTR2 | c.250T>C (p.Phe84Leu) n.718T>C | |
| X | g.116172530T>G | CA414337923 | AGTR2 | c.250T>G (p.Phe84Val) n.718T>G | |
| X | g.116172531T>A | CA414337924 | AGTR2 | c.251T>A (p.Phe84Tyr) n.719T>A | |
| X | g.116172531T>C | CA414337925 | AGTR2 | c.251T>C (p.Phe84Ser) n.719T>C | gnomAD v4 |
| X | g.116172531T>G | CA414337926 | AGTR2 | c.251T>G (p.Phe84Cys) n.719T>G | |
| X | g.116172532C>A | CA414337927 | AGTR2 | c.252C>A (p.Phe84Leu) n.720C>A | |
| X | g.116172532C>G | CA414337928 | AGTR2 | c.252C>G (p.Phe84Leu) n.720C>G | |
| X | g.116172532C>T | CA518449371 | AGTR2 | c.252C>T (p.Phe84=) n.720C>T | |
| X | g.116172533A>C | CA414337929 | AGTR2 | c.253A>C (p.Asn85His) n.721A>C | gnomAD v4 |
| X | g.116172533A>G | CA414337930 | AGTR2 | c.253A>G (p.Asn85Asp) n.721A>G | |
| X | g.116172533A>T | CA414337931 | AGTR2 | c.253A>T (p.Asn85Tyr) n.721A>T | |
| X | g.116172534A>C | CA414337932 | AGTR2 | c.254A>C (p.Asn85Thr) n.722A>C | |
| X | g.116172534A>G | CA414337934 | AGTR2 | c.254A>G (p.Asn85Ser) n.722A>G | gnomAD v4 |
| X | g.116172534A>T | CA414337933 | AGTR2 | c.254A>T (p.Asn85Ile) n.722A>T | |
| X | g.116172535C>A | CA414337935 | AGTR2 | c.255C>A (p.Asn85Lys) n.723C>A | COSMIC |
| X | g.116172535C>G | CA414337936 | AGTR2 | c.255C>G (p.Asn85Lys) n.723C>G | |
| X | g.116172535C>T | CA518449372 | AGTR2 | c.255C>T (p.Asn85=) n.723C>T | |
| X | g.116172536C>A | CA414337937 | AGTR2 | c.256C>A (p.Leu86Ile) n.724C>A | |
| X | g.116172536C>G | CA414337938 | AGTR2 | c.256C>G (p.Leu86Val) n.724C>G | |
| X | g.116172536C>T | CA414337939 | AGTR2 | c.256C>T (p.Leu86Phe) n.724C>T | |
| X | g.116172537T>A | CA414337940 | AGTR2 | c.257T>A (p.Leu86His) n.725T>A | |
| X | g.116172537T>C | CA414337941 | AGTR2 | c.257T>C (p.Leu86Pro) n.725T>C | |
| X | g.116172537T>G | CA414337942 | AGTR2 | c.257T>G (p.Leu86Arg) n.725T>G | |
| X | g.116172538C>A | CA518449378 | AGTR2 | c.258C>A (p.Leu86=) n.726C>A | |
| X | g.116172538C= | CA2453331739 | AGTR2 | c.258C= (p.Leu86=) n.726C= | |
| X | g.116172538C>G | CA518449379 | AGTR2 | c.258C>G (p.Leu86=) n.726C>G | |
| X | g.116172538C>T | CA10497250 | AGTR2 | c.258C>T (p.Leu86=) n.726C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| X | g.116172538_116172544delinsCGCTGTG | CA2453331740 | AGTR2 | c.258_264delinsCGCTGTG (p.Leu86=) n.726_732delinsCGCTGTG | |
| X | g.116172539G>A | CA414337944 | AGTR2 | c.259G>A (p.Ala87Thr) n.727G>A | dbSNP gnomAD v2 |
| X | g.116172539G>C | CA414337945 | AGTR2 | c.259G>C (p.Ala87Pro) n.727G>C | |
| X | g.116172539G= | CA2453331742 | AGTR2 | c.259G= (p.Ala87=) n.727G= | |
| X | g.116172539G>T | CA414337943 | AGTR2 | c.259G>T (p.Ala87Ser) n.727G>T | gnomAD v3 gnomAD v4 |
| X | g.116172543_116172548del | CA2453331741 | AGTR2 | c.263_268del (p.Val88_Ala89del) n.731_736del | dbSNP |
| X | g.116172540C>A | CA414337946 | AGTR2 | c.260C>A (p.Ala87Asp) n.728C>A | |
| X | g.116172540C>G | CA414337947 | AGTR2 | c.260C>G (p.Ala87Gly) n.728C>G | |
| X | g.116172540C>T | CA414337948 | AGTR2 | c.260C>T (p.Ala87Val) n.728C>T | |
| X | g.116172541T>A | CA518449389 | AGTR2 | c.261T>A (p.Ala87=) n.729T>A | |
| X | g.116172541T>C | CA518449391 | AGTR2 | c.261T>C (p.Ala87=) n.729T>C | |
| X | g.116172541T>G | CA518449390 | AGTR2 | c.261T>G (p.Ala87=) n.729T>G | |
| X | g.116172542G>A | CA414337949 | AGTR2 | c.262G>A (p.Val88Met) n.730G>A | dbSNP |
| X | g.116172542G>C | CA414337950 | AGTR2 | c.262G>C (p.Val88Leu) n.730G>C | |
| X | g.116172542G= | CA2453331743 | AGTR2 | c.262G= (p.Val88=) n.730G= | |
| X | g.116172542G>T | CA414337951 | AGTR2 | c.262G>T (p.Val88Leu) n.730G>T | |
| X | g.116172543T>A | CA414337952 | AGTR2 | c.263T>A (p.Val88Glu) n.731T>A | |
| X | g.116172543T>C | CA414337953 | AGTR2 | c.263T>C (p.Val88Ala) n.731T>C | |
| X | g.116172543T>G | CA414337954 | AGTR2 | c.263T>G (p.Val88Gly) n.731T>G | |
| X | g.116172544G>A | CA518449404 | AGTR2 | c.264G>A (p.Val88=) n.732G>A | dbSNP |
| X | g.116172544G>C | CA518449405 | AGTR2 | c.264G>C (p.Val88=) n.732G>C | |
| X | g.116172544G= | CA2453331744 | AGTR2 | c.264G= (p.Val88=) n.732G= | |
| X | g.116172544G>T | CA518449406 | AGTR2 | c.264G>T (p.Val88=) n.732G>T | |
| X | g.116172545G>A | CA414337955 | AGTR2 | c.265G>A (p.Ala89Thr) n.733G>A | |
| X | g.116172545G>C | CA414337956 | AGTR2 | c.265G>C (p.Ala89Pro) n.733G>C | |
| X | g.116172545G>T | CA414337957 | AGTR2 | c.265G>T (p.Ala89Ser) n.733G>T | |
| X | g.116172545_116172546insA | CA2579684211 | AGTR2 | c.265_266insA (p.Ala89AspfsTer2) n.733_734insA | gnomAD v4 |
| X | g.116172546C>A | CA414337960 | AGTR2 | c.266C>A (p.Ala89Asp) n.734C>A | gnomAD v4 |
| X | g.116172546C>G | CA414337958 | AGTR2 | c.266C>G (p.Ala89Gly) n.734C>G | |
| X | g.116172546C>T | CA414337959 | AGTR2 | c.266C>T (p.Ala89Val) n.734C>T | |
| X | g.116172547T>A | CA518449415 | AGTR2 | c.267T>A (p.Ala89=) n.735T>A | gnomAD v4 |
| X | g.116172547T>C | CA518449416 | AGTR2 | c.267T>C (p.Ala89=) n.735T>C | |
| X | g.116172547T>G | CA518449418 | AGTR2 | c.267T>G (p.Ala89=) n.735T>G | |
| X | g.116172548G>A | CA414337961 | AGTR2 | c.268G>A (p.Asp90Asn) n.736G>A | |
| X | g.116172548G>C | CA414337962 | AGTR2 | c.268G>C (p.Asp90His) n.736G>C | |
| X | g.116172548G>T | CA414337963 | AGTR2 | c.268G>T (p.Asp90Tyr) n.736G>T | |
| X | g.116172549A>C | CA414337964 | AGTR2 | c.269A>C (p.Asp90Ala) n.737A>C | |
| X | g.116172549A>G | CA414337965 | AGTR2 | c.269A>G (p.Asp90Gly) n.737A>G | |
| X | g.116172549A>T | CA414337966 | AGTR2 | c.269A>T (p.Asp90Val) n.737A>T | |
| X | g.116172550T>A | CA414337967 | AGTR2 | c.270T>A (p.Asp90Glu) n.738T>A | |
| X | g.116172550T>C | CA518449422 | AGTR2 | c.270T>C (p.Asp90=) n.738T>C | |
| X | g.116172550T>G | CA414337968 | AGTR2 | c.270T>G (p.Asp90Glu) n.738T>G | |
| X | g.116172551T>A | CA414337969 | AGTR2 | c.271T>A (p.Leu91Ile) n.739T>A | |
| X | g.116172551T>C | CA518449423 | AGTR2 | c.271T>C (p.Leu91=) n.739T>C | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172551T>G | CA414337970 | AGTR2 | c.271T>G (p.Leu91Val) n.739T>G | |
| X | g.116172551T= | CA2453331745 | AGTR2 | c.271T= (p.Leu91=) n.739T= | |
| X | g.116172552T>A | CA414337971 | AGTR2 | c.272T>A (p.Leu91Ter) n.740T>A | |
| X | g.116172552T>C | CA414337972 | AGTR2 | c.272T>C (p.Leu91Ser) n.740T>C | |
| X | g.116172552T>G | CA414337973 | AGTR2 | c.272T>G (p.Leu91Ter) n.740T>G | |
| X | g.116172553A>C | CA414337975 | AGTR2 | c.273A>C (p.Leu91Phe) n.741A>C | |
| X | g.116172553A>G | CA518449426 | AGTR2 | c.273A>G (p.Leu91=) n.741A>G | |
| X | g.116172553A>T | CA414337974 | AGTR2 | c.273A>T (p.Leu91Phe) n.741A>T | |
| X | g.116172554C>A | CA414337976 | AGTR2 | c.274C>A (p.Leu92Ile) n.742C>A | dbSNP |
| X | g.116172554C= | CA2453331746 | AGTR2 | c.274C= (p.Leu92=) n.742C= | |
| X | g.116172554C>G | CA414337978 | AGTR2 | c.274C>G (p.Leu92Val) n.742C>G | |
| X | g.116172554C>T | CA414337977 | AGTR2 | c.274C>T (p.Leu92Phe) n.742C>T | gnomAD v4 |
| X | g.116172555T>A | CA414337979 | AGTR2 | c.275T>A (p.Leu92His) n.743T>A | |
| X | g.116172555T>C | CA414337980 | AGTR2 | c.275T>C (p.Leu92Pro) n.743T>C | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172555T>G | CA414337981 | AGTR2 | c.275T>G (p.Leu92Arg) n.743T>G | |
| X | g.116172555T= | CA2453331747 | AGTR2 | c.275T= (p.Leu92=) n.743T= | |
| X | g.116172556C>A | CA518449431 | AGTR2 | c.276C>A (p.Leu92=) n.744C>A | |
| X | g.116172556C= | CA2453331748 | AGTR2 | c.276C= (p.Leu92=) n.744C= | |
| X | g.116172556C>G | CA518449432 | AGTR2 | c.276C>G (p.Leu92=) n.744C>G | |
| X | g.116172556C>T | CA518449434 | AGTR2 | c.276C>T (p.Leu92=) n.744C>T | dbSNP gnomAD v2 |
| X | g.116172557C>A | CA414337982 | AGTR2 | c.277C>A (p.Leu93Ile) n.745C>A | |
| X | g.116172557C>G | CA414337983 | AGTR2 | c.277C>G (p.Leu93Val) n.745C>G | |
| X | g.116172557C>T | CA414337984 | AGTR2 | c.277C>T (p.Leu93Phe) n.745C>T | dbSNP |
| X | g.116172557_116172558delinsCT | CA2453331749 | AGTR2 | c.277_278delinsCT (p.Leu93=) n.745_746delinsCT | |
| X | g.116172558T>A | CA414337985 | AGTR2 | c.278T>A (p.Leu93His) n.746T>A | |
| X | g.116172558T>C | CA414337986 | AGTR2 | c.278T>C (p.Leu93Pro) n.746T>C | |
| X | g.116172558T>G | CA414337987 | AGTR2 | c.278T>G (p.Leu93Arg) n.746T>G | |
| X | g.116172561del | CA870448915 | AGTR2 | c.281del (p.Leu94TrpfsTer22) n.749del | dbSNP |
| X | g.116172559T>A | CA518449440 | AGTR2 | c.279T>A (p.Leu93=) n.747T>A | |
| X | g.116172559T>C | CA518449441 | AGTR2 | c.279T>C (p.Leu93=) n.747T>C | gnomAD v4 |
| X | g.116172559T>G | CA518449443 | AGTR2 | c.279T>G (p.Leu93=) n.747T>G | |
| X | g.116172560T>A | CA414337988 | AGTR2 | c.280T>A (p.Leu94Met) n.748T>A | |
| X | g.116172560T>C | CA518449446 | AGTR2 | c.280T>C (p.Leu94=) n.748T>C | |
| X | g.116172560T>G | CA414337989 | AGTR2 | c.280T>G (p.Leu94Val) n.748T>G | |
| X | g.116172561T>A | CA414337991 | AGTR2 | c.281T>A (p.Leu94Ter) n.749T>A | |
| X | g.116172561T>C | CA334723684 | AGTR2 | c.281T>C (p.Leu94Ser) n.749T>C | dbSNP gnomAD v4 |
| X | g.116172561T>G | CA414337990 | AGTR2 | c.281T>G (p.Leu94Trp) n.749T>G | |
| X | g.116172561T= | CA2453331750 | AGTR2 | c.281T= (p.Leu94=) n.749T= | |
| X | g.116172562G>A | CA518449451 | AGTR2 | c.282G>A (p.Leu94=) n.750G>A | |
| X | g.116172562G>C | CA414337992 | AGTR2 | c.282G>C (p.Leu94Phe) n.750G>C | |
| X | g.116172562G>T | CA414337993 | AGTR2 | c.282G>T (p.Leu94Phe) n.750G>T | |
| X | g.116172563G>A | CA414337994 | AGTR2 | c.283G>A (p.Ala95Thr) n.751G>A | |
| X | g.116172563G>C | CA414337995 | AGTR2 | c.283G>C (p.Ala95Pro) n.751G>C | |
| X | g.116172563G>T | CA414337996 | AGTR2 | c.283G>T (p.Ala95Ser) n.751G>T | gnomAD v4 |
| X | g.116172564del | CA2507996919 | AGTR2 | c.284del (p.Ala95ValfsTer21) n.752del | |
| X | g.116172564C>A | CA414337997 | AGTR2 | c.284C>A (p.Ala95Asp) n.752C>A | |
| X | g.116172564C= | CA2453331751 | AGTR2 | c.284C= (p.Ala95=) n.752C= | |
| X | g.116172564C>G | CA414337998 | AGTR2 | c.284C>G (p.Ala95Gly) n.752C>G | |
| X | g.116172564C>T | CA414337999 | AGTR2 | c.284C>T (p.Ala95Val) n.752C>T | gnomAD v4 |
| X | g.116172565T>A | CA518449459 | AGTR2 | c.285T>A (p.Ala95=) n.753T>A | |
| X | g.116172565T>C | CA518449458 | AGTR2 | c.285T>C (p.Ala95=) n.753T>C | dbSNP |
| X | g.116172565T>G | CA518449457 | AGTR2 | c.285T>G (p.Ala95=) n.753T>G | |
| X | g.116172565T= | CA2453331752 | AGTR2 | c.285T= (p.Ala95=) n.753T= | |
| X | g.116172565_116172568dup | CA644065624 | AGTR2 | c.285_288dup (p.Leu97TyrfsTer12) n.753_756dup | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172566A>C | CA414338000 | AGTR2 | c.286A>C (p.Thr96Pro) n.754A>C | |
| X | g.116172566A>G | CA414338001 | AGTR2 | c.286A>G (p.Thr96Ala) n.754A>G | |
| X | g.116172566A>T | CA414338002 | AGTR2 | c.286A>T (p.Thr96Ser) n.754A>T | |
| X | g.116172567C>A | CA414338004 | AGTR2 | c.287C>A (p.Thr96Asn) n.755C>A | |
| X | g.116172567C>G | CA414338005 | AGTR2 | c.287C>G (p.Thr96Ser) n.755C>G | |
| X | g.116172567C>T | CA414338003 | AGTR2 | c.287C>T (p.Thr96Ile) n.755C>T | |
| X | g.116172568T>A | CA518449463 | AGTR2 | c.288T>A (p.Thr96=) n.756T>A | |
| X | g.116172568T>C | CA518449468 | AGTR2 | c.288T>C (p.Thr96=) n.756T>C | |
| X | g.116172568T>G | CA518449465 | AGTR2 | c.288T>G (p.Thr96=) n.756T>G | |
| X | g.116172569C>A | CA414338006 | AGTR2 | c.289C>A (p.Leu97Ile) n.757C>A | |
| X | g.116172569C>G | CA414338007 | AGTR2 | c.289C>G (p.Leu97Val) n.757C>G | |
| X | g.116172569C>T | CA414338008 | AGTR2 | c.289C>T (p.Leu97Phe) n.757C>T | |
| X | g.116172570T>A | CA414338009 | AGTR2 | c.290T>A (p.Leu97His) n.758T>A | |
| X | g.116172570T>C | CA414338010 | AGTR2 | c.290T>C (p.Leu97Pro) n.758T>C | |
| X | g.116172570T>G | CA414338011 | AGTR2 | c.290T>G (p.Leu97Arg) n.758T>G | |
| X | g.116172571T>A | CA518449476 | AGTR2 | c.291T>A (p.Leu97=) n.759T>A | |
| X | g.116172571T>C | CA518449477 | AGTR2 | c.291T>C (p.Leu97=) n.759T>C | |
| X | g.116172571T>G | CA518449480 | AGTR2 | c.291T>G (p.Leu97=) n.759T>G | |
| X | g.116172572C>A | CA414338014 | AGTR2 | c.292C>A (p.Pro98Thr) n.760C>A | |
| X | g.116172572C>G | CA414338012 | AGTR2 | c.292C>G (p.Pro98Ala) n.760C>G | |
| X | g.116172572C>T | CA414338013 | AGTR2 | c.292C>T (p.Pro98Ser) n.760C>T | gnomAD v4 |
| X | g.116172573C>A | CA414338015 | AGTR2 | c.293C>A (p.Pro98His) n.761C>A | |
| X | g.116172573C>G | CA414338016 | AGTR2 | c.293C>G (p.Pro98Arg) n.761C>G | |
| X | g.116172573C>T | CA414338017 | AGTR2 | c.293C>T (p.Pro98Leu) n.761C>T | gnomAD v4 |
| X | g.116172574T>A | CA518449483 | AGTR2 | c.294T>A (p.Pro98=) n.762T>A | |
| X | g.116172574T>C | CA518449484 | AGTR2 | c.294T>C (p.Pro98=) n.762T>C | |
| X | g.116172574T>G | CA518449486 | AGTR2 | c.294T>G (p.Pro98=) n.762T>G | |
| X | g.116172575C>A | CA414338018 | AGTR2 | c.295C>A (p.Leu99Ile) n.763C>A | |
| X | g.116172575C>G | CA414338019 | AGTR2 | c.295C>G (p.Leu99Val) n.763C>G | |
| X | g.116172575C>T | CA518449493 | AGTR2 | c.295C>T (p.Leu99=) n.763C>T | |
| X | g.116172576T>A | CA414338020 | AGTR2 | c.296T>A (p.Leu99Gln) n.764T>A | |
| X | g.116172576T>C | CA10497251 | AGTR2 | c.296T>C (p.Leu99Pro) n.764T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.116172576T>G | CA414338021 | AGTR2 | c.296T>G (p.Leu99Arg) n.764T>G | |
| X | g.116172576T= | CA2453331753 | AGTR2 | c.296T= (p.Leu99=) n.764T= | |
| X | g.116172577A>C | CA518449495 | AGTR2 | c.297A>C (p.Leu99=) n.765A>C | |
| X | g.116172577A>G | CA518449496 | AGTR2 | c.297A>G (p.Leu99=) n.765A>G | |
| X | g.116172577A>T | CA518449497 | AGTR2 | c.297A>T (p.Leu99=) n.765A>T | gnomAD v4 |
| X | g.116172578T>A | CA414338022 | AGTR2 | c.298T>A (p.Trp100Arg) n.766T>A | |
| X | g.116172578T>C | CA10497252 | AGTR2 | c.298T>C (p.Trp100Arg) n.766T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172578T>G | CA414338023 | AGTR2 | c.298T>G (p.Trp100Gly) n.766T>G | |
| X | g.116172578T= | CA2453331755 | AGTR2 | c.298T= (p.Trp100=) n.766T= | |
| X | g.116172578_116172579delinsTG | CA2453331754 | AGTR2 | c.298_299delinsTG (p.Trp100=) n.766_767delinsTG | |
| X | g.116172579G>A | CA414338024 | AGTR2 | c.299G>A (p.Trp100Ter) n.767G>A | |
| X | g.116172579G>C | CA414338025 | AGTR2 | c.299G>C (p.Trp100Ser) n.767G>C | |
| X | g.116172579G>T | CA414338026 | AGTR2 | c.299G>T (p.Trp100Leu) n.767G>T | |
| X | g.116172581del | CA644065625 | AGTR2 | c.301del (p.Ala101GlnfsTer15) n.769del | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172580G>A | CA414338027 | AGTR2 | c.300G>A (p.Trp100Ter) n.768G>A | |
| X | g.116172580G>C | CA414338028 | AGTR2 | c.300G>C (p.Trp100Cys) n.768G>C | |
| X | g.116172580G>T | CA414338029 | AGTR2 | c.300G>T (p.Trp100Cys) n.768G>T | |
| X | g.116172581G>A | CA414338030 | AGTR2 | c.301G>A (p.Ala101Thr) n.769G>A | |
| X | g.116172581G>C | CA414338031 | AGTR2 | c.301G>C (p.Ala101Pro) n.769G>C | |
| X | g.116172581G>T | CA414338032 | AGTR2 | c.301G>T (p.Ala101Ser) n.769G>T | |
| X | g.116172582C>A | CA414338035 | AGTR2 | c.302C>A (p.Ala101Glu) n.770C>A | COSMIC |
| X | g.116172582C>G | CA414338034 | AGTR2 | c.302C>G (p.Ala101Gly) n.770C>G | |
| X | g.116172582C>T | CA414338033 | AGTR2 | c.302C>T (p.Ala101Val) n.770C>T |