| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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 | |
| 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 |