| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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 | |
| X | g.116172583A>C | CA518449520 | AGTR2 | c.303A>C (p.Ala101=) n.771A>C | gnomAD v4 |
| X | g.116172583A>G | CA518449522 | AGTR2 | c.303A>G (p.Ala101=) n.771A>G | |
| X | g.116172583A>T | CA518449521 | AGTR2 | c.303A>T (p.Ala101=) n.771A>T | |
| X | g.116172584A>C | CA414338036 | AGTR2 | c.304A>C (p.Thr102Pro) n.772A>C | |
| X | g.116172584A>G | CA414338038 | AGTR2 | c.304A>G (p.Thr102Ala) n.772A>G | |
| X | g.116172584A>T | CA414338037 | AGTR2 | c.304A>T (p.Thr102Ser) n.772A>T | |
| X | g.116172584_116172585delinsGT | CA645603886 | AGTR2 | c.304_305delinsGT (p.Thr102Val) n.772_773delinsGT | COSMIC |
| X | g.116172585C>A | CA414338039 | AGTR2 | c.305C>A (p.Thr102Asn) n.773C>A | |
| X | g.116172585C>G | CA414338041 | AGTR2 | c.305C>G (p.Thr102Ser) n.773C>G | |
| X | g.116172585C>T | CA414338040 | AGTR2 | c.305C>T (p.Thr102Ile) n.773C>T | gnomAD v4 |
| X | g.116172586C>A | CA518449533 | AGTR2 | c.306C>A (p.Thr102=) n.774C>A | |
| X | g.116172586C= | CA2453331756 | AGTR2 | c.306C= (p.Thr102=) n.774C= | |
| X | g.116172586C>G | CA518449536 | AGTR2 | c.306C>G (p.Thr102=) n.774C>G | |
| X | g.116172586C>T | CA518449537 | AGTR2 | c.306C>T (p.Thr102=) n.774C>T | dbSNP |
| X | g.116172587T>A | CA414338042 | AGTR2 | c.307T>A (p.Tyr103Asn) n.775T>A | |
| X | g.116172587T>C | CA414338043 | AGTR2 | c.307T>C (p.Tyr103His) n.775T>C | |
| X | g.116172587T>G | CA414338044 | AGTR2 | c.307T>G (p.Tyr103Asp) n.775T>G | |
| X | g.116172591_116172593dup | CA2694510862 | AGTR2 | c.311_313dup (p.Tyr104_Ser105insTyr) n.779_781dup | gnomAD v4 |
| X | g.116172588A= | CA2453331757 | AGTR2 | c.308A= (p.Tyr103=) n.776A= | |
| X | g.116172588A>C | CA414338045 | AGTR2 | c.308A>C (p.Tyr103Ser) n.776A>C | |
| X | g.116172588A>G | CA10497253 | AGTR2 | c.308A>G (p.Tyr103Cys) n.776A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172588A>T | CA414338046 | AGTR2 | c.308A>T (p.Tyr103Phe) n.776A>T | |
| X | g.116172588_116172594delinsATTATTC | CA2453331758 | AGTR2 | c.308_314delinsATTATTC (p.Tyr103=) n.776_782delinsATTATTC | |
| X | g.116172589T>A | CA414338047 | AGTR2 | c.309T>A (p.Tyr103Ter) n.777T>A | |
| X | g.116172589T>C | CA518449547 | AGTR2 | c.309T>C (p.Tyr103=) n.777T>C | gnomAD v4 |
| X | g.116172589T>G | CA414338048 | AGTR2 | c.309T>G (p.Tyr103Ter) n.777T>G | COSMIC |
| X | g.116172593_116172598del | CA1136568906 | AGTR2 | c.313_318del (p.Ser105_Tyr106del) n.781_786del | dbSNP gnomAD v3 gnomAD v4 |
| X | g.116172590T>A | CA414338049 | AGTR2 | c.310T>A (p.Tyr104Asn) n.778T>A | |
| X | g.116172590T>C | CA414338050 | AGTR2 | c.310T>C (p.Tyr104His) n.778T>C | dbSNP |
| X | g.116172590T>G | CA414338051 | AGTR2 | c.310T>G (p.Tyr104Asp) n.778T>G | |
| X | g.116172591A>C | CA414338054 | AGTR2 | c.311A>C (p.Tyr104Ser) n.779A>C | |
| X | g.116172591A>G | CA414338052 | AGTR2 | c.311A>G (p.Tyr104Cys) n.779A>G | |
| X | g.116172591A>T | CA414338053 | AGTR2 | c.311A>T (p.Tyr104Phe) n.779A>T | |
| X | g.116172591dup | CA2823125653 | AGTR2 | c.311dup (p.Tyr104Ter) n.779dup | |
| X | g.116172592T>A | CA414338055 | AGTR2 | c.312T>A (p.Tyr104Ter) n.780T>A | dbSNP |
| X | g.116172592T>C | CA518449553 | AGTR2 | c.312T>C (p.Tyr104=) n.780T>C | |
| X | g.116172592T>G | CA414338056 | AGTR2 | c.312T>G (p.Tyr104Ter) n.780T>G | gnomAD v4 |
| X | g.116172592T= | CA2453331759 | AGTR2 | c.312T= (p.Tyr104=) n.780T= | |
| X | g.116172593T>A | CA414338057 | AGTR2 | c.313T>A (p.Ser105Thr) n.781T>A | |
| X | g.116172593T>C | CA414338058 | AGTR2 | c.313T>C (p.Ser105Pro) n.781T>C | |
| X | g.116172593T>G | CA414338059 | AGTR2 | c.313T>G (p.Ser105Ala) n.781T>G | |
| X | g.116172594C>A | CA414338060 | AGTR2 | c.314C>A (p.Ser105Tyr) n.782C>A | |
| X | g.116172594C= | CA2453331760 | AGTR2 | c.314C= (p.Ser105=) n.782C= | |
| X | g.116172594C>G | CA414338061 | AGTR2 | c.314C>G (p.Ser105Cys) n.782C>G | ClinVar dbSNP |
| X | g.116172594C>T | CA414338062 | AGTR2 | c.314C>T (p.Ser105Phe) n.782C>T | |
| X | g.116172595T>A | CA518449558 | AGTR2 | c.315T>A (p.Ser105=) n.783T>A | |
| X | g.116172595T>C | CA518449563 | AGTR2 | c.315T>C (p.Ser105=) n.783T>C | |
| X | g.116172595T>G | CA518449564 | AGTR2 | c.315T>G (p.Ser105=) n.783T>G | |
| X | g.116172596T>A | CA414338063 | AGTR2 | c.316T>A (p.Tyr106Asn) n.784T>A | |
| X | g.116172596T>C | CA414338064 | AGTR2 | c.316T>C (p.Tyr106His) n.784T>C | |
| X | g.116172596T>G | CA414338065 | AGTR2 | c.316T>G (p.Tyr106Asp) n.784T>G | |
| X | g.116172597A= | CA2453331761 | AGTR2 | c.317A= (p.Tyr106=) n.785A= | |
| X | g.116172597A>C | CA414338068 | AGTR2 | c.317A>C (p.Tyr106Ser) n.785A>C | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172597A>G | CA414338067 | AGTR2 | c.317A>G (p.Tyr106Cys) n.785A>G | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172597A>T | CA414338066 | AGTR2 | c.317A>T (p.Tyr106Phe) n.785A>T | |
| X | g.116172598T>A | CA414338070 | AGTR2 | c.318T>A (p.Tyr106Ter) n.786T>A | |
| X | g.116172598T>C | CA518449573 | AGTR2 | c.318T>C (p.Tyr106=) n.786T>C | gnomAD v4 |
| X | g.116172598T>G | CA414338069 | AGTR2 | c.318T>G (p.Tyr106Ter) n.786T>G | |
| X | g.116172599A>C | CA518449576 | AGTR2 | c.319A>C (p.Arg107=) n.787A>C | |
| X | g.116172599A>G | CA414338071 | AGTR2 | c.319A>G (p.Arg107Gly) n.787A>G | |
| X | g.116172599A>T | CA414338072 | AGTR2 | c.319A>T (p.Arg107Ter) n.787A>T | |
| X | g.116172600G>A | CA414338073 | AGTR2 | c.320G>A (p.Arg107Lys) n.788G>A | |
| X | g.116172600G>C | CA414338074 | AGTR2 | c.320G>C (p.Arg107Thr) n.788G>C | COSMIC |
| X | g.116172600G>T | CA414338075 | AGTR2 | c.320G>T (p.Arg107Ile) n.788G>T | |
| X | g.116172600_116172602delinsGAT | CA2453331762 | AGTR2 | c.320_322delinsGAT (p.Arg107=) n.788_790delinsGAT | |
| X | g.116172601A>C | CA414338077 | AGTR2 | c.321A>C (p.Arg107Ser) n.789A>C | |
| X | g.116172601A>G | CA518449589 | AGTR2 | c.321A>G (p.Arg107=) n.789A>G | |
| X | g.116172601A>T | CA414338076 | AGTR2 | c.321A>T (p.Arg107Ser) n.789A>T | |
| X | g.116172603_116172604del | CA644065626 | AGTR2 | c.323_324del (p.Tyr108Ter) n.791_792del | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172602T>A | CA414338078 | AGTR2 | c.322T>A (p.Tyr108Asn) n.790T>A | |
| X | g.116172602T>C | CA414338079 | AGTR2 | c.322T>C (p.Tyr108His) n.790T>C | |
| X | g.116172602T>G | CA414338080 | AGTR2 | c.322T>G (p.Tyr108Asp) n.790T>G | |
| X | g.116172603A= | CA2453331763 | AGTR2 | c.323A= (p.Tyr108=) n.791A= | |
| X | g.116172603A>C | CA414338081 | AGTR2 | c.323A>C (p.Tyr108Ser) n.791A>C | |
| X | g.116172603A>G | CA414338082 | AGTR2 | c.323A>G (p.Tyr108Cys) n.791A>G | dbSNP |
| X | g.116172603A>T | CA414338083 | AGTR2 | c.323A>T (p.Tyr108Phe) n.791A>T | |
| X | g.116172604T>A | CA414338084 | AGTR2 | c.324T>A (p.Tyr108Ter) n.792T>A | |
| X | g.116172604T>C | CA10497254 | AGTR2 | c.324T>C (p.Tyr108=) n.792T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172604T>G | CA414338085 | AGTR2 | c.324T>G (p.Tyr108Ter) n.792T>G | gnomAD v4 |
| X | g.116172604T= | CA2453331764 | AGTR2 | c.324T= (p.Tyr108=) n.792T= | |
| X | g.116172605G>A | CA414338086 | AGTR2 | c.325G>A (p.Asp109Asn) n.793G>A | |
| X | g.116172605G>C | CA414338087 | AGTR2 | c.325G>C (p.Asp109His) n.793G>C | gnomAD v4 |
| X | g.116172605G>T | CA414338088 | AGTR2 | c.325G>T (p.Asp109Tyr) n.793G>T | gnomAD v4 |
| X | g.116172606A>C | CA414338089 | AGTR2 | c.326A>C (p.Asp109Ala) n.794A>C | |
| X | g.116172606A>G | CA414338090 | AGTR2 | c.326A>G (p.Asp109Gly) n.794A>G | |
| X | g.116172606A>T | CA414338091 | AGTR2 | c.326A>T (p.Asp109Val) n.794A>T | |
| X | g.116172607C>A | CA414338092 | AGTR2 | c.327C>A (p.Asp109Glu) n.795C>A | |
| X | g.116172607C>G | CA414338093 | AGTR2 | c.327C>G (p.Asp109Glu) n.795C>G | |
| X | g.116172607C>T | CA518449598 | AGTR2 | c.327C>T (p.Asp109=) n.795C>T | gnomAD v4 |
| X | g.116172608T>A | CA414338094 | AGTR2 | c.328T>A (p.Trp110Arg) n.796T>A | |
| X | g.116172608T>C | CA414338095 | AGTR2 | c.328T>C (p.Trp110Arg) n.796T>C | gnomAD v4 |
| X | g.116172608T>G | CA414338096 | AGTR2 | c.328T>G (p.Trp110Gly) n.796T>G | dbSNP gnomAD v4 |
| X | g.116172608T= | CA2453331765 | AGTR2 | c.328T= (p.Trp110=) n.796T= | |
| X | g.116172609G>A | CA414338098 | AGTR2 | c.329G>A (p.Trp110Ter) n.797G>A | |
| X | g.116172609G>C | CA414338099 | AGTR2 | c.329G>C (p.Trp110Ser) n.797G>C | |
| X | g.116172609G>T | CA414338097 | AGTR2 | c.329G>T (p.Trp110Leu) n.797G>T | |
| X | g.116172610G>A | CA414338100 | AGTR2 | c.330G>A (p.Trp110Ter) n.798G>A | |
| X | g.116172610G>C | CA414338102 | AGTR2 | c.330G>C (p.Trp110Cys) n.798G>C | |
| X | g.116172610G>T | CA414338101 | AGTR2 | c.330G>T (p.Trp110Cys) n.798G>T | |
| X | g.116172611C>A | CA414338103 | AGTR2 | c.331C>A (p.Leu111Ile) n.799C>A | |
| X | g.116172611C>G | CA414338104 | AGTR2 | c.331C>G (p.Leu111Val) n.799C>G | |
| X | g.116172611C>T | CA414338105 | AGTR2 | c.331C>T (p.Leu111Phe) n.799C>T | gnomAD v4 |
| X | g.116172612T>A | CA414338106 | AGTR2 | c.332T>A (p.Leu111His) n.800T>A | gnomAD v4 |
| X | g.116172612T>C | CA414338107 | AGTR2 | c.332T>C (p.Leu111Pro) n.800T>C | |
| X | g.116172612T>G | CA414338108 | AGTR2 | c.332T>G (p.Leu111Arg) n.800T>G | |
| X | g.116172613C>A | CA518449610 | AGTR2 | c.333C>A (p.Leu111=) n.801C>A | |
| X | g.116172613C>G | CA518449612 | AGTR2 | c.333C>G (p.Leu111=) n.801C>G | |
| X | g.116172613C>T | CA518449615 | AGTR2 | c.333C>T (p.Leu111=) n.801C>T | gnomAD v4 COSMIC |
| X | g.116172614T>A | CA414338109 | AGTR2 | c.334T>A (p.Phe112Ile) n.802T>A | gnomAD v4 |
| X | g.116172614T>C | CA414338110 | AGTR2 | c.334T>C (p.Phe112Leu) n.802T>C | |
| X | g.116172614T>G | CA414338111 | AGTR2 | c.334T>G (p.Phe112Val) n.802T>G | |
| X | g.116172616dup | CA2694510863 | AGTR2 | c.336dup (p.Gly113TrpfsTer29) n.804dup | gnomAD v4 |
| X | g.116172615T>A | CA414338112 | AGTR2 | c.335T>A (p.Phe112Tyr) n.803T>A | |
| X | g.116172615T>C | CA414338113 | AGTR2 | c.335T>C (p.Phe112Ser) n.803T>C | |
| X | g.116172615T>G | CA414338114 | AGTR2 | c.335T>G (p.Phe112Cys) n.803T>G | |
| X | g.116172616T>A | CA414338115 | AGTR2 | c.336T>A (p.Phe112Leu) n.804T>A | gnomAD v4 |
| X | g.116172616T>C | CA518449624 | AGTR2 | c.336T>C (p.Phe112=) n.804T>C | |
| X | g.116172616T>G | CA414338116 | AGTR2 | c.336T>G (p.Phe112Leu) n.804T>G | |
| X | g.116172617G>A | CA414338117 | AGTR2 | c.337G>A (p.Gly113Arg) n.805G>A | |
| X | g.116172617G>C | CA414338118 | AGTR2 | c.337G>C (p.Gly113Arg) n.805G>C | |
| X | g.116172617G>T | CA414338119 | AGTR2 | c.337G>T (p.Gly113Ter) n.805G>T | |
| X | g.116172618G>A | CA414338120 | AGTR2 | c.338G>A (p.Gly113Glu) n.806G>A | |
| X | g.116172618G>C | CA414338121 | AGTR2 | c.338G>C (p.Gly113Ala) n.806G>C | |
| X | g.116172618G>T | CA414338122 | AGTR2 | c.338G>T (p.Gly113Val) n.806G>T | |
| X | g.116172619A>C | CA518449633 | AGTR2 | c.339A>C (p.Gly113=) n.807A>C | |
| X | g.116172619A>G | CA518449635 | AGTR2 | c.339A>G (p.Gly113=) n.807A>G | |
| X | g.116172619A>T | CA518449637 | AGTR2 | c.339A>T (p.Gly113=) n.807A>T | |
| X | g.116172620C>A | CA414338123 | AGTR2 | c.340C>A (p.Pro114Thr) n.808C>A | |
| X | g.116172620C>G | CA414338124 | AGTR2 | c.340C>G (p.Pro114Ala) n.808C>G | |
| X | g.116172620C>T | CA414338125 | AGTR2 | c.340C>T (p.Pro114Ser) n.808C>T | |
| X | g.116172621C>A | CA414338126 | AGTR2 | c.341C>A (p.Pro114His) n.809C>A | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172621C= | CA2453331766 | AGTR2 | c.341C= (p.Pro114=) n.809C= | |
| X | g.116172621C>G | CA414338127 | AGTR2 | c.341C>G (p.Pro114Arg) n.809C>G | |
| X | g.116172621C>T | CA414338128 | AGTR2 | c.341C>T (p.Pro114Leu) n.809C>T | |
| X | g.116172622T>A | CA518449646 | AGTR2 | c.342T>A (p.Pro114=) n.810T>A | |
| X | g.116172622T>C | CA518449649 | AGTR2 | c.342T>C (p.Pro114=) n.810T>C | dbSNP |
| X | g.116172622T>G | CA518449651 | AGTR2 | c.342T>G (p.Pro114=) n.810T>G | |
| X | g.116172622T= | CA2453331767 | AGTR2 | c.342T= (p.Pro114=) n.810T= | |
| X | g.116172623G>A | CA414338129 | AGTR2 | c.343G>A (p.Val115Met) n.811G>A | |
| X | g.116172623G>C | CA414338131 | AGTR2 | c.343G>C (p.Val115Leu) n.811G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172623G= | CA2453331768 | AGTR2 | c.343G= (p.Val115=) n.811G= | |
| X | g.116172623G>T | CA414338130 | AGTR2 | c.343G>T (p.Val115Leu) n.811G>T | |
| X | g.116172624T>A | CA414338132 | AGTR2 | c.344T>A (p.Val115Glu) n.812T>A | |
| X | g.116172624T>C | CA414338133 | AGTR2 | c.344T>C (p.Val115Ala) n.812T>C | |
| X | g.116172624T>G | CA414338134 | AGTR2 | c.344T>G (p.Val115Gly) n.812T>G | |
| X | g.116172625G>A | CA518449660 | AGTR2 | c.345G>A (p.Val115=) n.813G>A | dbSNP gnomAD v4 |
| X | g.116172625G>C | CA518449662 | AGTR2 | c.345G>C (p.Val115=) n.813G>C | |
| X | g.116172625G= | CA2453331769 | AGTR2 | c.345G= (p.Val115=) n.813G= | |
| X | g.116172625G>T | CA518449661 | AGTR2 | c.345G>T (p.Val115=) n.813G>T | |
| X | g.116172626A>C | CA414338135 | AGTR2 | c.346A>C (p.Met116Leu) n.814A>C | |
| X | g.116172626A>G | CA414338136 | AGTR2 | c.346A>G (p.Met116Val) n.814A>G | |
| X | g.116172626A>T | CA414338137 | AGTR2 | c.346A>T (p.Met116Leu) n.814A>T | |
| X | g.116172627T>A | CA414338138 | AGTR2 | c.347T>A (p.Met116Lys) n.815T>A | |
| X | g.116172627T>C | CA10497255 | AGTR2 | c.347T>C (p.Met116Thr) n.815T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172627T>G | CA414338139 | AGTR2 | c.347T>G (p.Met116Arg) n.815T>G | |
| X | g.116172627T= | CA2453331770 | AGTR2 | c.347T= (p.Met116=) n.815T= | |
| X | g.116172628G>A | CA414338140 | AGTR2 | c.348G>A (p.Met116Ile) n.816G>A | dbSNP gnomAD v4 |
| X | g.116172628G>C | CA414338141 | AGTR2 | c.348G>C (p.Met116Ile) n.816G>C | |
| X | g.116172628G= | CA2453331771 | AGTR2 | c.348G= (p.Met116=) n.816G= | |
| X | g.116172628G>T | CA414338142 | AGTR2 | c.348G>T (p.Met116Ile) n.816G>T | |
| X | g.116172629T>A | CA414338145 | AGTR2 | c.349T>A (p.Cys117Ser) n.817T>A | |
| X | g.116172629T>C | CA414338143 | AGTR2 | c.349T>C (p.Cys117Arg) n.817T>C | dbSNP gnomAD v3 gnomAD v4 |
| X | g.116172629T>G | CA414338144 | AGTR2 | c.349T>G (p.Cys117Gly) n.817T>G | |
| X | g.116172629T= | CA2453331772 | AGTR2 | c.349T= (p.Cys117=) n.817T= | |
| X | g.116172630G>A | CA414338146 | AGTR2 | c.350G>A (p.Cys117Tyr) n.818G>A | gnomAD v4 |
| X | g.116172630G>C | CA414338147 | AGTR2 | c.350G>C (p.Cys117Ser) n.818G>C | |
| X | g.116172630G= | CA2453331773 | AGTR2 | c.350G= (p.Cys117=) n.818G= | |
| X | g.116172630G>T | CA414338148 | AGTR2 | c.350G>T (p.Cys117Phe) n.818G>T | dbSNP |
| X | g.116172631C>A | CA414338149 | AGTR2 | c.351C>A (p.Cys117Ter) n.819C>A | |
| X | g.116172631C>G | CA414338150 | AGTR2 | c.351C>G (p.Cys117Trp) n.819C>G | |
| X | g.116172631C>T | CA518449675 | AGTR2 | c.351C>T (p.Cys117=) n.819C>T | |
| X | g.116172631_116172633delinsCAA | CA2453331774 | AGTR2 | c.351_353delinsCAA (p.Cys117=) n.819_821delinsCAA | |
| X | g.116172632A>C | CA414338151 | AGTR2 | c.352A>C (p.Lys118Gln) n.820A>C | |
| X | g.116172632A>G | CA414338152 | AGTR2 | c.352A>G (p.Lys118Glu) n.820A>G | |
| X | g.116172632A>T | CA414338153 | AGTR2 | c.352A>T (p.Lys118Ter) n.820A>T | |
| X | g.116172634del | CA518449678 | AGTR2 | c.354del (p.Val119PhefsTer8) n.822del | |
| X | g.116172633_116172634del | CA870449060 | AGTR2 | c.353_354del (p.Lys118SerfsTer23) n.821_822del | dbSNP gnomAD v4 |
| X | g.116172633A>C | CA414338154 | AGTR2 | c.353A>C (p.Lys118Thr) n.821A>C | |
| X | g.116172633A>G | CA414338155 | AGTR2 | c.353A>G (p.Lys118Arg) n.821A>G | |
| X | g.116172633A>T | CA414338156 | AGTR2 | c.353A>T (p.Lys118Ile) n.821A>T | |
| X | g.116172634A>C | CA414338158 | AGTR2 | c.354A>C (p.Lys118Asn) n.822A>C | |
| X | g.116172634A>G | CA518449687 | AGTR2 | c.354A>G (p.Lys118=) n.822A>G | |
| X | g.116172634A>T | CA414338157 | AGTR2 | c.354A>T (p.Lys118Asn) n.822A>T | |
| X | g.116172635G>A | CA414338159 | AGTR2 | c.355G>A (p.Val119Ile) n.823G>A | |
| X | g.116172635G>C | CA414338161 | AGTR2 | c.355G>C (p.Val119Leu) n.823G>C | |
| X | g.116172635G>T | CA414338160 | AGTR2 | c.355G>T (p.Val119Phe) n.823G>T | |
| X | g.116172636_116172641del | CA2694510864 | AGTR2 | c.356_361del (p.Val119_Phe120del) n.824_829del | gnomAD v4 |
| X | g.116172636T>A | CA414338162 | AGTR2 | c.356T>A (p.Val119Asp) n.824T>A | |
| X | g.116172636T>C | CA414338164 | AGTR2 | c.356T>C (p.Val119Ala) n.824T>C | |
| X | g.116172636T>G | CA414338163 | AGTR2 | c.356T>G (p.Val119Gly) n.824T>G | |
| X | g.116172637T>A | CA518449694 | AGTR2 | c.357T>A (p.Val119=) n.825T>A | |
| X | g.116172637T>C | CA518449695 | AGTR2 | c.357T>C (p.Val119=) n.825T>C | |
| X | g.116172637T>G | CA518449696 | AGTR2 | c.357T>G (p.Val119=) n.825T>G | gnomAD v3 gnomAD v4 |
| X | g.116172638T>A | CA414338165 | AGTR2 | c.358T>A (p.Phe120Ile) n.826T>A | COSMIC |
| X | g.116172638T>C | CA414338166 | AGTR2 | c.358T>C (p.Phe120Leu) n.826T>C | |
| X | g.116172638T>G | CA414338167 | AGTR2 | c.358T>G (p.Phe120Val) n.826T>G | |
| X | g.116172639T>A | CA414338168 | AGTR2 | c.359T>A (p.Phe120Tyr) n.827T>A | |
| X | g.116172639T>C | CA414338169 | AGTR2 | c.359T>C (p.Phe120Ser) n.827T>C | |
| X | g.116172639T>G | CA414338170 | AGTR2 | c.359T>G (p.Phe120Cys) n.827T>G | |
| X | g.116172640T>A | CA414338171 | AGTR2 | c.360T>A (p.Phe120Leu) n.828T>A | |
| X | g.116172640T>C | CA518449703 | AGTR2 | c.360T>C (p.Phe120=) n.828T>C | gnomAD v4 |
| X | g.116172640T>G | CA414338172 | AGTR2 | c.360T>G (p.Phe120Leu) n.828T>G | |
| X | g.116172641G>A | CA414338173 | AGTR2 | c.361G>A (p.Gly121Ser) n.829G>A | |
| X | g.116172641G>C | CA414338174 | AGTR2 | c.361G>C (p.Gly121Arg) n.829G>C | |
| X | g.116172641G>T | CA414338175 | AGTR2 | c.361G>T (p.Gly121Cys) n.829G>T | gnomAD v4 |
| X | g.116172642G>A | CA414338176 | AGTR2 | c.362G>A (p.Gly121Asp) n.830G>A | |
| X | g.116172642G>C | CA414338178 | AGTR2 | c.362G>C (p.Gly121Ala) n.830G>C | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172642G= | CA2453331775 | AGTR2 | c.362G= (p.Gly121=) n.830G= | |
| X | g.116172642G>T | CA414338177 | AGTR2 | c.362G>T (p.Gly121Val) n.830G>T | |
| X | g.116172643T>A | CA518449711 | AGTR2 | c.363T>A (p.Gly121=) n.831T>A | |
| X | g.116172643T>C | CA518449712 | AGTR2 | c.363T>C (p.Gly121=) n.831T>C | |
| X | g.116172643T>G | CA518449714 | AGTR2 | c.363T>G (p.Gly121=) n.831T>G | |
| X | g.116172644T>A | CA414338179 | AGTR2 | c.364T>A (p.Ser122Thr) n.832T>A | |
| X | g.116172644T>C | CA414338180 | AGTR2 | c.364T>C (p.Ser122Pro) n.832T>C | |
| X | g.116172644T>G | CA414338181 | AGTR2 | c.364T>G (p.Ser122Ala) n.832T>G | |
| X | g.116172645C>A | CA10497256 | AGTR2 | c.365C>A (p.Ser122Tyr) n.833C>A | dbSNP ExAC gnomAD v2 COSMIC |
| X | g.116172645C= | CA2453331776 | AGTR2 | c.365C= (p.Ser122=) n.833C= | |
| X | g.116172645C>G | CA414338182 | AGTR2 | c.365C>G (p.Ser122Cys) n.833C>G | |
| X | g.116172645C>T | CA414338183 | AGTR2 | c.365C>T (p.Ser122Phe) n.833C>T | |
| X | g.116172646T>A | CA518449725 | AGTR2 | c.366T>A (p.Ser122=) n.834T>A | |
| X | g.116172646T>C | CA518449723 | AGTR2 | c.366T>C (p.Ser122=) n.834T>C | |
| X | g.116172646T>G | CA518449724 | AGTR2 | c.366T>G (p.Ser122=) n.834T>G | |
| X | g.116172647T>A | CA414338184 | AGTR2 | c.367T>A (p.Phe123Ile) n.835T>A | |
| X | g.116172647T>C | CA414338185 | AGTR2 | c.367T>C (p.Phe123Leu) n.835T>C | |
| X | g.116172647T>G | CA414338186 | AGTR2 | c.367T>G (p.Phe123Val) n.835T>G | |
| X | g.116172648T>A | CA414338188 | AGTR2 | c.368T>A (p.Phe123Tyr) n.836T>A | |
| X | g.116172648T>C | CA414338189 | AGTR2 | c.368T>C (p.Phe123Ser) n.836T>C | |
| X | g.116172648T>G | CA414338187 | AGTR2 | c.368T>G (p.Phe123Cys) n.836T>G | |
| X | g.116172649T>A | CA414338190 | AGTR2 | c.369T>A (p.Phe123Leu) n.837T>A | |
| X | g.116172649T>C | CA518449735 | AGTR2 | c.369T>C (p.Phe123=) n.837T>C | |
| X | g.116172649T>G | CA414338191 | AGTR2 | c.369T>G (p.Phe123Leu) n.837T>G | |
| X | g.116172650C>A | CA414338192 | AGTR2 | c.370C>A (p.Leu124Ile) n.838C>A | |
| X | g.116172650C>G | CA414338193 | AGTR2 | c.370C>G (p.Leu124Val) n.838C>G | |
| X | g.116172650C>T | CA414338194 | AGTR2 | c.370C>T (p.Leu124Phe) n.838C>T | |
| X | g.116172651T>A | CA414338195 | AGTR2 | c.371T>A (p.Leu124His) n.839T>A | |
| X | g.116172651T>C | CA414338196 | AGTR2 | c.371T>C (p.Leu124Pro) n.839T>C | |
| X | g.116172651T>G | CA414338197 | AGTR2 | c.371T>G (p.Leu124Arg) n.839T>G | |
| X | g.116172652T>A | CA518449740 | AGTR2 | c.372T>A (p.Leu124=) n.840T>A | |
| X | g.116172652T>C | CA518449744 | AGTR2 | c.372T>C (p.Leu124=) n.840T>C | dbSNP gnomAD v3 gnomAD v4 |
| X | g.116172652T>G | CA518449741 | AGTR2 | c.372T>G (p.Leu124=) n.840T>G | |
| X | g.116172652T= | CA2453331777 | AGTR2 | c.372T= (p.Leu124=) n.840T= | |
| X | g.116172653A>C | CA414338198 | AGTR2 | c.373A>C (p.Thr125Pro) n.841A>C | |
| X | g.116172653A>G | CA414338199 | AGTR2 | c.373A>G (p.Thr125Ala) n.841A>G | |
| X | g.116172653A>T | CA414338200 | AGTR2 | c.373A>T (p.Thr125Ser) n.841A>T |