| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.116172389C>A | CA414337614 | AGTR2 | c.109C>A (p.Gln37Lys) n.577C>A | |
| X | g.116172389C= | CA2453331685 | AGTR2 | c.109C= (p.Gln37=) n.577C= | |
| X | g.116172389C>G | CA10497229 | AGTR2 | c.109C>G (p.Gln37Glu) n.577C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172389C>T | CA414337615 | AGTR2 | c.109C>T (p.Gln37Ter) n.577C>T | |
| X | g.116172390A= | CA2453331686 | AGTR2 | c.110A= (p.Gln37=) n.578A= | |
| X | g.116172390A>C | CA414337616 | AGTR2 | c.110A>C (p.Gln37Pro) n.578A>C | |
| X | g.116172390A>G | CA414337617 | AGTR2 | c.110A>G (p.Gln37Arg) n.578A>G | dbSNP gnomAD v3 gnomAD v4 |
| X | g.116172390A>T | CA414337618 | AGTR2 | c.110A>T (p.Gln37Leu) n.578A>T | |
| X | g.116172391G>A | CA518449162 | AGTR2 | c.111G>A (p.Gln37=) n.579G>A | gnomAD v4 |
| X | g.116172391G>C | CA414337619 | AGTR2 | c.111G>C (p.Gln37His) n.579G>C | |
| X | g.116172391G= | CA2453331687 | AGTR2 | c.111G= (p.Gln37=) n.579G= | |
| X | g.116172391G>T | CA334723679 | AGTR2 | c.111G>T (p.Gln37His) n.579G>T | dbSNP |
| X | g.116172392A>C | CA414337620 | AGTR2 | c.112A>C (p.Lys38Gln) n.580A>C | |
| X | g.116172392A>G | CA414337621 | AGTR2 | c.112A>G (p.Lys38Glu) n.580A>G | |
| X | g.116172392A>T | CA414337622 | AGTR2 | c.112A>T (p.Lys38Ter) n.580A>T | |
| X | g.116172393A>C | CA414337625 | AGTR2 | c.113A>C (p.Lys38Thr) n.581A>C | |
| X | g.116172393A>G | CA414337623 | AGTR2 | c.113A>G (p.Lys38Arg) n.581A>G | |
| X | g.116172393A>T | CA414337624 | AGTR2 | c.113A>T (p.Lys38Ile) n.581A>T | |
| X | g.116172394A>C | CA414337626 | AGTR2 | c.114A>C (p.Lys38Asn) n.582A>C | |
| X | g.116172394A>G | CA518449163 | AGTR2 | c.114A>G (p.Lys38=) n.582A>G | |
| X | g.116172394A>T | CA414337627 | AGTR2 | c.114A>T (p.Lys38Asn) n.582A>T | |
| X | g.116172395C>A | CA414337628 | AGTR2 | c.115C>A (p.Pro39Thr) n.583C>A | dbSNP gnomAD v4 |
| X | g.116172395C= | CA2453331688 | AGTR2 | c.115C= (p.Pro39=) n.583C= | |
| X | g.116172395C>G | CA414337629 | AGTR2 | c.115C>G (p.Pro39Ala) n.583C>G | |
| X | g.116172395C>T | CA414337630 | AGTR2 | c.115C>T (p.Pro39Ser) n.583C>T | |
| X | g.116172396C>A | CA414337631 | AGTR2 | c.116C>A (p.Pro39Gln) n.584C>A | |
| X | g.116172396C= | CA2453331689 | AGTR2 | c.116C= (p.Pro39=) n.584C= | |
| X | g.116172396C>G | CA414337632 | AGTR2 | c.116C>G (p.Pro39Arg) n.584C>G | |
| X | g.116172396C>T | CA414337633 | AGTR2 | c.116C>T (p.Pro39Leu) n.584C>T | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172397A>C | CA518449166 | AGTR2 | c.117A>C (p.Pro39=) n.585A>C | |
| X | g.116172397A>G | CA518449165 | AGTR2 | c.117A>G (p.Pro39=) n.585A>G | |
| X | g.116172397A>T | CA518449164 | AGTR2 | c.117A>T (p.Pro39=) n.585A>T | |
| X | g.116172398T>A | CA10497230 | AGTR2 | c.118T>A (p.Ser40Thr) n.586T>A | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| X | g.116172398T>C | CA414337634 | AGTR2 | c.118T>C (p.Ser40Pro) n.586T>C | |
| X | g.116172398T>G | CA414337635 | AGTR2 | c.118T>G (p.Ser40Ala) n.586T>G | |
| X | g.116172398T= | CA2453331690 | AGTR2 | c.118T= (p.Ser40=) n.586T= | |
| X | g.116172399C>A | CA414337636 | AGTR2 | c.119C>A (p.Ser40Ter) n.587C>A | gnomAD v4 |
| X | g.116172399C= | CA2453331691 | AGTR2 | c.119C= (p.Ser40=) n.587C= | |
| X | g.116172399C>G | CA414337637 | AGTR2 | c.119C>G (p.Ser40Ter) n.587C>G | |
| X | g.116172399C>T | CA10497231 | AGTR2 | c.119C>T (p.Ser40Leu) n.587C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.116172400A>C | CA518449169 | AGTR2 | c.120A>C (p.Ser40=) n.588A>C | |
| X | g.116172400A>G | CA518449167 | AGTR2 | c.120A>G (p.Ser40=) n.588A>G | |
| X | g.116172400A>T | CA518449168 | AGTR2 | c.120A>T (p.Ser40=) n.588A>T | |
| X | g.116172401G>A | CA221173 | AGTR2 | c.121G>A (p.Asp41Asn) n.589G>A | ClinVar dbSNP gnomAD v4 |
| X | g.116172401G>C | CA414337638 | AGTR2 | c.121G>C (p.Asp41His) n.589G>C | COSMIC |
| X | g.116172401G= | CA2453331692 | AGTR2 | c.121G= (p.Asp41=) n.589G= | |
| X | g.116172401G>T | CA414337639 | AGTR2 | c.121G>T (p.Asp41Tyr) n.589G>T | |
| X | g.116172402A>C | CA414337640 | AGTR2 | c.122A>C (p.Asp41Ala) n.590A>C | |
| X | g.116172402A>G | CA414337641 | AGTR2 | c.122A>G (p.Asp41Gly) n.590A>G | gnomAD v4 |
| X | g.116172402A>T | CA414337642 | AGTR2 | c.122A>T (p.Asp41Val) n.590A>T | |
| X | g.116172403T>A | CA414337643 | AGTR2 | c.123T>A (p.Asp41Glu) n.591T>A | gnomAD v4 |
| X | g.116172403T>C | CA10497232 | AGTR2 | c.123T>C (p.Asp41=) n.591T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.116172403T>G | CA414337644 | AGTR2 | c.123T>G (p.Asp41Glu) n.591T>G | |
| X | g.116172403T= | CA2453331693 | AGTR2 | c.123T= (p.Asp41=) n.591T= | |
| X | g.116172404A>C | CA414337645 | AGTR2 | c.124A>C (p.Lys42Gln) n.592A>C | |
| X | g.116172404A>G | CA414337646 | AGTR2 | c.124A>G (p.Lys42Glu) n.592A>G | |
| X | g.116172404A>T | CA414337647 | AGTR2 | c.124A>T (p.Lys42Ter) n.592A>T | |
| X | g.116172405A>C | CA414337649 | AGTR2 | c.125A>C (p.Lys42Thr) n.593A>C | |
| X | g.116172405A>G | CA414337650 | AGTR2 | c.125A>G (p.Lys42Arg) n.593A>G | |
| X | g.116172405A>T | CA414337648 | AGTR2 | c.125A>T (p.Lys42Met) n.593A>T | |
| X | g.116172406G>A | CA334723680 | AGTR2 | c.126G>A (p.Lys42=) n.594G>A | dbSNP gnomAD v4 |
| X | g.116172406G>C | CA414337651 | AGTR2 | c.126G>C (p.Lys42Asn) n.594G>C | |
| X | g.116172406G= | CA2453331694 | AGTR2 | c.126G= (p.Lys42=) n.594G= | |
| X | g.116172406G>T | CA414337652 | AGTR2 | c.126G>T (p.Lys42Asn) n.594G>T | |
| X | g.116172407C>A | CA334723681 | AGTR2 | c.127C>A (p.His43Asn) n.595C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172407C= | CA2453331695 | AGTR2 | c.127C= (p.His43=) n.595C= | |
| X | g.116172407C>G | CA414337653 | AGTR2 | c.127C>G (p.His43Asp) n.595C>G | |
| X | g.116172407C>T | CA10497233 | AGTR2 | c.127C>T (p.His43Tyr) n.595C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172408A>C | CA414337654 | AGTR2 | c.128A>C (p.His43Pro) n.596A>C | |
| X | g.116172408A>G | CA414337656 | AGTR2 | c.128A>G (p.His43Arg) n.596A>G | |
| X | g.116172408A>T | CA414337655 | AGTR2 | c.128A>T (p.His43Leu) n.596A>T | |
| X | g.116172409T>A | CA414337657 | AGTR2 | c.129T>A (p.His43Gln) n.597T>A | |
| X | g.116172409T>C | CA518449170 | AGTR2 | c.129T>C (p.His43=) n.597T>C | |
| X | g.116172409T>G | CA414337658 | AGTR2 | c.129T>G (p.His43Gln) n.597T>G | |
| X | g.116172410T>A | CA414337659 | AGTR2 | c.130T>A (p.Leu44Ile) n.598T>A | |
| X | g.116172410T>C | CA518449171 | AGTR2 | c.130T>C (p.Leu44=) n.598T>C | |
| X | g.116172410T>G | CA10497234 | AGTR2 | c.130T>G (p.Leu44Val) n.598T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172410T= | CA2453331696 | AGTR2 | c.130T= (p.Leu44=) n.598T= | |
| X | g.116172411T>A | CA414337662 | AGTR2 | c.131T>A (p.Leu44Ter) n.599T>A | |
| X | g.116172411T>C | CA414337661 | AGTR2 | c.131T>C (p.Leu44Ser) n.599T>C | |
| X | g.116172411T>G | CA414337660 | AGTR2 | c.131T>G (p.Leu44Ter) n.599T>G | |
| X | g.116172412A>C | CA414337663 | AGTR2 | c.132A>C (p.Leu44Phe) n.600A>C | gnomAD v3 gnomAD v4 |
| X | g.116172412A>G | CA518449172 | AGTR2 | c.132A>G (p.Leu44=) n.600A>G | |
| X | g.116172412A>T | CA414337664 | AGTR2 | c.132A>T (p.Leu44Phe) n.600A>T | |
| X | g.116172413G>A | CA414337665 | AGTR2 | c.133G>A (p.Asp45Asn) n.601G>A | COSMIC |
| X | g.116172413G>C | CA414337666 | AGTR2 | c.133G>C (p.Asp45His) n.601G>C | |
| X | g.116172413G>T | CA414337667 | AGTR2 | c.133G>T (p.Asp45Tyr) n.601G>T | COSMIC |
| X | g.116172414A>C | CA414337668 | AGTR2 | c.134A>C (p.Asp45Ala) n.602A>C | |
| X | g.116172414A>G | CA414337669 | AGTR2 | c.134A>G (p.Asp45Gly) n.602A>G | gnomAD v4 |
| X | g.116172414A>T | CA414337670 | AGTR2 | c.134A>T (p.Asp45Val) n.602A>T | |
| X | g.116172415T>A | CA414337671 | AGTR2 | c.135T>A (p.Asp45Glu) n.603T>A | |
| X | g.116172415T>C | CA518449173 | AGTR2 | c.135T>C (p.Asp45=) n.603T>C | gnomAD v4 |
| X | g.116172415T>G | CA414337672 | AGTR2 | c.135T>G (p.Asp45Glu) n.603T>G | |
| X | g.116172416G>A | CA414337673 | AGTR2 | c.136G>A (p.Ala46Thr) n.604G>A | |
| X | g.116172416G>C | CA414337674 | AGTR2 | c.136G>C (p.Ala46Pro) n.604G>C | |
| X | g.116172416G>T | CA414337675 | AGTR2 | c.136G>T (p.Ala46Ser) n.604G>T | |
| X | g.116172417C>A | CA414337678 | AGTR2 | c.137C>A (p.Ala46Glu) n.605C>A | |
| X | g.116172417C>G | CA414337677 | AGTR2 | c.137C>G (p.Ala46Gly) n.605C>G | |
| X | g.116172417C>T | CA414337676 | AGTR2 | c.137C>T (p.Ala46Val) n.605C>T | |
| X | g.116172418A>C | CA518449176 | AGTR2 | c.138A>C (p.Ala46=) n.606A>C | |
| X | g.116172418A>G | CA518449175 | AGTR2 | c.138A>G (p.Ala46=) n.606A>G | |
| X | g.116172418A>T | CA518449174 | AGTR2 | c.138A>T (p.Ala46=) n.606A>T | |
| X | g.116172419A>C | CA414337679 | AGTR2 | c.139A>C (p.Ile47Leu) n.607A>C | |
| X | g.116172419A>G | CA414337680 | AGTR2 | c.139A>G (p.Ile47Val) n.607A>G | |
| X | g.116172419A>T | CA414337681 | AGTR2 | c.139A>T (p.Ile47Phe) n.607A>T | |
| X | g.116172420T>A | CA414337682 | AGTR2 | c.140T>A (p.Ile47Asn) n.608T>A | |
| X | g.116172420T>C | CA414337683 | AGTR2 | c.140T>C (p.Ile47Thr) n.608T>C | gnomAD v4 |
| X | g.116172420T>G | CA414337684 | AGTR2 | c.140T>G (p.Ile47Ser) n.608T>G | |
| X | g.116172421T>A | CA518449177 | AGTR2 | c.141T>A (p.Ile47=) n.609T>A | |
| X | g.116172421T>C | CA518449178 | AGTR2 | c.141T>C (p.Ile47=) n.609T>C | |
| X | g.116172421T>G | CA414337685 | AGTR2 | c.141T>G (p.Ile47Met) n.609T>G | |
| X | g.116172422C>A | CA414337686 | AGTR2 | c.142C>A (p.Pro48Thr) n.610C>A | |
| X | g.116172422C= | CA2453331697 | AGTR2 | c.142C= (p.Pro48=) n.610C= | |
| X | g.116172422C>G | CA414337687 | AGTR2 | c.142C>G (p.Pro48Ala) n.610C>G | |
| X | g.116172422C>T | CA414337688 | AGTR2 | c.142C>T (p.Pro48Ser) n.610C>T | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| X | g.116172423C>A | CA414337689 | AGTR2 | c.143C>A (p.Pro48His) n.611C>A | dbSNP gnomAD v2 |
| X | g.116172423C= | CA2453331698 | AGTR2 | c.143C= (p.Pro48=) n.611C= | |
| X | g.116172423C>G | CA414337690 | AGTR2 | c.143C>G (p.Pro48Arg) n.611C>G | |
| X | g.116172423C>T | CA414337691 | AGTR2 | c.143C>T (p.Pro48Leu) n.611C>T | |
| X | g.116172424T>A | CA518449179 | AGTR2 | c.144T>A (p.Pro48=) n.612T>A | |
| X | g.116172424T>C | CA518449180 | AGTR2 | c.144T>C (p.Pro48=) n.612T>C | dbSNP gnomAD v3 gnomAD v4 |
| X | g.116172424T>G | CA518449181 | AGTR2 | c.144T>G (p.Pro48=) n.612T>G | |
| X | g.116172424T= | CA2453331699 | AGTR2 | c.144T= (p.Pro48=) n.612T= | |
| X | g.116172425A>C | CA414337694 | AGTR2 | c.145A>C (p.Ile49Leu) n.613A>C | |
| X | g.116172425A>G | CA414337693 | AGTR2 | c.145A>G (p.Ile49Val) n.613A>G | ClinVar gnomAD v4 |
| X | g.116172425A>T | CA414337692 | AGTR2 | c.145A>T (p.Ile49Phe) n.613A>T | |
| X | g.116172426T>A | CA414337697 | AGTR2 | c.146T>A (p.Ile49Asn) n.614T>A | |
| X | g.116172426T>C | CA414337695 | AGTR2 | c.146T>C (p.Ile49Thr) n.614T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172426T>G | CA414337696 | AGTR2 | c.146T>G (p.Ile49Ser) n.614T>G | |
| X | g.116172426T= | CA2453331700 | AGTR2 | c.146T= (p.Ile49=) n.614T= | |
| X | g.116172427T>A | CA518449182 | AGTR2 | c.147T>A (p.Ile49=) n.615T>A | |
| X | g.116172427T>C | CA518449183 | AGTR2 | c.147T>C (p.Ile49=) n.615T>C | |
| X | g.116172427T>G | CA414337698 | AGTR2 | c.147T>G (p.Ile49Met) n.615T>G | |
| X | g.116172428C>A | CA414337699 | AGTR2 | c.148C>A (p.Leu50Ile) n.616C>A | |
| X | g.116172428C>G | CA414337700 | AGTR2 | c.148C>G (p.Leu50Val) n.616C>G | gnomAD v4 |
| X | g.116172428C>T | CA414337701 | AGTR2 | c.148C>T (p.Leu50Phe) n.616C>T | |
| X | g.116172429T>A | CA414337702 | AGTR2 | c.149T>A (p.Leu50His) n.617T>A | |
| X | g.116172429T>C | CA10497235 | AGTR2 | c.149T>C (p.Leu50Pro) n.617T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172429T>G | CA414337703 | AGTR2 | c.149T>G (p.Leu50Arg) n.617T>G | |
| X | g.116172429T= | CA2453331701 | AGTR2 | c.149T= (p.Leu50=) n.617T= | |
| X | g.116172430T>A | CA518449184 | AGTR2 | c.150T>A (p.Leu50=) n.618T>A | |
| X | g.116172430T>C | CA518449185 | AGTR2 | c.150T>C (p.Leu50=) n.618T>C | |
| X | g.116172430T>G | CA518449186 | AGTR2 | c.150T>G (p.Leu50=) n.618T>G | |
| X | g.116172430_116172433delinsTTAC | CA2453331702 | AGTR2 | c.150_153delinsTTAC (p.Leu50=) n.618_621delinsTTAC | |
| X | g.116172431T>A | CA414337704 | AGTR2 | c.151T>A (p.Tyr51Asn) n.619T>A | |
| X | g.116172431T>C | CA414337705 | AGTR2 | c.151T>C (p.Tyr51His) n.619T>C | |
| X | g.116172431T>G | CA414337706 | AGTR2 | c.151T>G (p.Tyr51Asp) n.619T>G | |
| X | g.116172434_116172436del | CA2453331703 | AGTR2 | c.154_156del (p.Tyr52del) n.622_624del | dbSNP |
| X | g.116172432A>C | CA414337708 | AGTR2 | c.152A>C (p.Tyr51Ser) n.620A>C | |
| X | g.116172432A>G | CA414337709 | AGTR2 | c.152A>G (p.Tyr51Cys) n.620A>G | |
| X | g.116172432A>T | CA414337707 | AGTR2 | c.152A>T (p.Tyr51Phe) n.620A>T | |
| X | g.116172433C>A | CA414337710 | AGTR2 | c.153C>A (p.Tyr51Ter) n.621C>A | |
| X | g.116172433C>G | CA414337711 | AGTR2 | c.153C>G (p.Tyr51Ter) n.621C>G | COSMIC |
| X | g.116172433C>T | CA518449187 | AGTR2 | c.153C>T (p.Tyr51=) n.621C>T | |
| X | g.116172434T>A | CA414337712 | AGTR2 | c.154T>A (p.Tyr52Asn) n.622T>A | |
| X | g.116172434T>C | CA414337713 | AGTR2 | c.154T>C (p.Tyr52His) n.622T>C | |
| X | g.116172434T>G | CA10497236 | AGTR2 | c.154T>G (p.Tyr52Asp) n.622T>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.116172434T= | CA2453331704 | AGTR2 | c.154T= (p.Tyr52=) n.622T= | |
| X | g.116172435A>C | CA414337716 | AGTR2 | c.155A>C (p.Tyr52Ser) n.623A>C | |
| X | g.116172435A>G | CA414337714 | AGTR2 | c.155A>G (p.Tyr52Cys) n.623A>G | |
| X | g.116172435A>T | CA414337715 | AGTR2 | c.155A>T (p.Tyr52Phe) n.623A>T | |
| X | g.116172436C>A | CA414337717 | AGTR2 | c.156C>A (p.Tyr52Ter) n.624C>A | |
| X | g.116172436C= | CA2453331705 | AGTR2 | c.156C= (p.Tyr52=) n.624C= | |
| X | g.116172436C>G | CA414337718 | AGTR2 | c.156C>G (p.Tyr52Ter) n.624C>G | |
| X | g.116172436C>T | CA10497237 | AGTR2 | c.156C>T (p.Tyr52=) n.624C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.116172437A= | CA2453331706 | AGTR2 | c.157A= (p.Ile53=) n.625A= | |
| X | g.116172437A>C | CA414337719 | AGTR2 | c.157A>C (p.Ile53Leu) n.625A>C | |
| X | g.116172437A>G | CA414337720 | AGTR2 | c.157A>G (p.Ile53Val) n.625A>G | |
| X | g.116172437A>T | CA229239 | AGTR2 | c.157A>T (p.Ile53Phe) n.625A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172438T>A | CA414337722 | AGTR2 | c.158T>A (p.Ile53Asn) n.626T>A | |
| X | g.116172438T>C | CA414337723 | AGTR2 | c.158T>C (p.Ile53Thr) n.626T>C | dbSNP gnomAD v4 |
| X | g.116172438T>G | CA414337721 | AGTR2 | c.158T>G (p.Ile53Ser) n.626T>G | |
| X | g.116172438T= | CA2453331707 | AGTR2 | c.158T= (p.Ile53=) n.626T= | |
| X | g.116172439T>A | CA518449188 | AGTR2 | c.159T>A (p.Ile53=) n.627T>A | gnomAD v4 |
| X | g.116172439T>C | CA518449189 | AGTR2 | c.159T>C (p.Ile53=) n.627T>C | |
| X | g.116172439T>G | CA414337724 | AGTR2 | c.159T>G (p.Ile53Met) n.627T>G | |
| X | g.116172440A>C | CA414337727 | AGTR2 | c.160A>C (p.Ile54Leu) n.628A>C | |
| X | g.116172440A>G | CA414337725 | AGTR2 | c.160A>G (p.Ile54Val) n.628A>G | gnomAD v4 |
| X | g.116172440A>T | CA414337726 | AGTR2 | c.160A>T (p.Ile54Leu) n.628A>T | |
| X | g.116172441T>A | CA414337728 | AGTR2 | c.161T>A (p.Ile54Lys) n.629T>A | |
| X | g.116172441T>C | CA414337729 | AGTR2 | c.161T>C (p.Ile54Thr) n.629T>C | |
| X | g.116172441T>G | CA414337730 | AGTR2 | c.161T>G (p.Ile54Arg) n.629T>G | |
| X | g.116172442A>C | CA518449190 | AGTR2 | c.162A>C (p.Ile54=) n.630A>C | |
| X | g.116172442A>G | CA414337731 | AGTR2 | c.162A>G (p.Ile54Met) n.630A>G | |
| X | g.116172442A>T | CA518449191 | AGTR2 | c.162A>T (p.Ile54=) n.630A>T | |
| X | g.116172443T>A | CA414337734 | AGTR2 | c.163T>A (p.Phe55Ile) n.631T>A | dbSNP gnomAD v3 gnomAD v4 |
| X | g.116172443T>C | CA414337732 | AGTR2 | c.163T>C (p.Phe55Leu) n.631T>C | dbSNP |
| X | g.116172443T>G | CA414337733 | AGTR2 | c.163T>G (p.Phe55Val) n.631T>G | |
| X | g.116172443T= | CA2453331708 | AGTR2 | c.163T= (p.Phe55=) n.631T= | |
| X | g.116172444T>A | CA414337735 | AGTR2 | c.164T>A (p.Phe55Tyr) n.632T>A | |
| X | g.116172444T>C | CA414337736 | AGTR2 | c.164T>C (p.Phe55Ser) n.632T>C | |
| X | g.116172444T>G | CA414337737 | AGTR2 | c.164T>G (p.Phe55Cys) n.632T>G | |
| X | g.116172445T>A | CA414337738 | AGTR2 | c.165T>A (p.Phe55Leu) n.633T>A | |
| X | g.116172445T>C | CA518449192 | AGTR2 | c.165T>C (p.Phe55=) n.633T>C | |
| X | g.116172445T>G | CA414337739 | AGTR2 | c.165T>G (p.Phe55Leu) n.633T>G | |
| X | g.116172446G>A | CA414337740 | AGTR2 | c.166G>A (p.Val56Ile) n.634G>A | |
| X | g.116172446G>C | CA414337742 | AGTR2 | c.166G>C (p.Val56Leu) n.634G>C | |
| X | g.116172446G= | CA2453331709 | AGTR2 | c.166G= (p.Val56=) n.634G= | |
| X | g.116172446G>T | CA414337741 | AGTR2 | c.166G>T (p.Val56Leu) n.634G>T | dbSNP gnomAD v4 |
| X | g.116172446_116172447insGATTTCTGGTCAATATTGGATTATACTGGATTATACTGGATTA | CA644065607 | AGTR2 | c.166_167insGATTTCTGGTCAATATTGGATTATACTGGATTATACTGGATTA (p.Val56GlyfsTer35) n.634_635insGATTTCTGGTCAATATTGGATTATACTGGATTATACTGGATTA | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172447T>A | CA414337743 | AGTR2 | c.167T>A (p.Val56Glu) n.635T>A | |
| X | g.116172447T>C | CA414337744 | AGTR2 | c.167T>C (p.Val56Ala) n.635T>C | |
| X | g.116172447T>G | CA414337745 | AGTR2 | c.167T>G (p.Val56Gly) n.635T>G | |
| X | g.116172448A>C | CA518449193 | AGTR2 | c.168A>C (p.Val56=) n.636A>C | |
| X | g.116172448A>G | CA518449194 | AGTR2 | c.168A>G (p.Val56=) n.636A>G | |
| X | g.116172448A>T | CA518449195 | AGTR2 | c.168A>T (p.Val56=) n.636A>T | |
| X | g.116172449A>C | CA414337746 | AGTR2 | c.169A>C (p.Ile57Leu) n.637A>C | |
| X | g.116172449A>G | CA414337747 | AGTR2 | c.169A>G (p.Ile57Val) n.637A>G | gnomAD v4 |
| X | g.116172449A>T | CA414337748 | AGTR2 | c.169A>T (p.Ile57Phe) n.637A>T | |
| X | g.116172450T>A | CA414337749 | AGTR2 | c.170T>A (p.Ile57Asn) n.638T>A | |
| X | g.116172450T>C | CA10497238 | AGTR2 | c.170T>C (p.Ile57Thr) n.638T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172450T>G | CA414337750 | AGTR2 | c.170T>G (p.Ile57Ser) n.638T>G | |
| X | g.116172450T= | CA2453331710 | AGTR2 | c.170T= (p.Ile57=) n.638T= | |
| X | g.116172451T>A | CA518449197 | AGTR2 | c.171T>A (p.Ile57=) n.639T>A | |
| X | g.116172451T>C | CA518449196 | AGTR2 | c.171T>C (p.Ile57=) n.639T>C | |
| X | g.116172451T>G | CA414337751 | AGTR2 | c.171T>G (p.Ile57Met) n.639T>G | |
| X | g.116172452G>A | CA414337754 | AGTR2 | c.172G>A (p.Gly58Arg) n.640G>A | gnomAD v4 COSMIC |
| X | g.116172452G>C | CA414337753 | AGTR2 | c.172G>C (p.Gly58Arg) n.640G>C | |
| X | g.116172452G>T | CA414337752 | AGTR2 | c.172G>T (p.Gly58Ter) n.640G>T | |
| X | g.116172453G>A | CA414337755 | AGTR2 | c.173G>A (p.Gly58Glu) n.641G>A | COSMIC |
| X | g.116172453G>C | CA414337756 | AGTR2 | c.173G>C (p.Gly58Ala) n.641G>C | |
| X | g.116172453G>T | CA414337757 | AGTR2 | c.173G>T (p.Gly58Val) n.641G>T | |
| X | g.116172454A>C | CA518449198 | AGTR2 | c.174A>C (p.Gly58=) n.642A>C | |
| X | g.116172454A>G | CA518449199 | AGTR2 | c.174A>G (p.Gly58=) n.642A>G | |
| X | g.116172454A>T | CA518449200 | AGTR2 | c.174A>T (p.Gly58=) n.642A>T | |
| X | g.116172455T>A | CA414337758 | AGTR2 | c.175T>A (p.Phe59Ile) n.643T>A | |
| X | g.116172455T>C | CA414337759 | AGTR2 | c.175T>C (p.Phe59Leu) n.643T>C | gnomAD v4 |
| X | g.116172455T>G | CA414337760 | AGTR2 | c.175T>G (p.Phe59Val) n.643T>G | |
| X | g.116172456T>A | CA414337761 | AGTR2 | c.176T>A (p.Phe59Tyr) n.644T>A | |
| X | g.116172456T>C | CA414337762 | AGTR2 | c.176T>C (p.Phe59Ser) n.644T>C | |
| X | g.116172456T>G | CA414337763 | AGTR2 | c.176T>G (p.Phe59Cys) n.644T>G | |
| X | g.116172457T>A | CA414337764 | AGTR2 | c.177T>A (p.Phe59Leu) n.645T>A | |
| X | g.116172457T>C | CA518449201 | AGTR2 | c.177T>C (p.Phe59=) n.645T>C | |
| X | g.116172457T>G | CA414337765 | AGTR2 | c.177T>G (p.Phe59Leu) n.645T>G | |
| X | g.116172458C>A | CA414337766 | AGTR2 | c.178C>A (p.Leu60Met) n.646C>A | |
| X | g.116172458C= | CA2453331711 | AGTR2 | c.178C= (p.Leu60=) n.646C= | |
| X | g.116172458C>G | CA414337767 | AGTR2 | c.178C>G (p.Leu60Val) n.646C>G | dbSNP |
| X | g.116172458C>T | CA518449202 | AGTR2 | c.178C>T (p.Leu60=) n.646C>T | COSMIC |
| X | g.116172459T>A | CA414337770 | AGTR2 | c.179T>A (p.Leu60Gln) n.647T>A | |
| X | g.116172459T>C | CA414337768 | AGTR2 | c.179T>C (p.Leu60Pro) n.647T>C | |
| X | g.116172459T>G | CA414337769 | AGTR2 | c.179T>G (p.Leu60Arg) n.647T>G | |
| X | g.116172460G>A | CA518449203 | AGTR2 | c.180G>A (p.Leu60=) n.648G>A | gnomAD v4 |
| X | g.116172460G>C | CA518449204 | AGTR2 | c.180G>C (p.Leu60=) n.648G>C | |
| X | g.116172460G>T | CA518449205 | AGTR2 | c.180G>T (p.Leu60=) n.648G>T | |
| X | g.116172461G>A | CA10497240 | AGTR2 | c.181G>A (p.Val61Ile) n.649G>A | dbSNP ExAC gnomAD v4 |
| X | g.116172461G>C | CA414337771 | AGTR2 | c.181G>C (p.Val61Leu) n.649G>C | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172461G= | CA2453331712 | AGTR2 | c.181G= (p.Val61=) n.649G= | |
| X | g.116172461G>T | CA10497239 | AGTR2 | c.181G>T (p.Val61Phe) n.649G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.116172462T>A | CA414337772 | AGTR2 | c.182T>A (p.Val61Asp) n.650T>A | |
| X | g.116172462T>C | CA414337773 | AGTR2 | c.182T>C (p.Val61Ala) n.650T>C | |
| X | g.116172462T>G | CA414337774 | AGTR2 | c.182T>G (p.Val61Gly) n.650T>G | |
| X | g.116172462_116172463insA | CA2694510860 | AGTR2 | c.182_183insA (p.Asn62GlnfsTer15) n.650_651insA | gnomAD v4 |
| X | g.116172463C>A | CA518449206 | AGTR2 | c.183C>A (p.Val61=) n.651C>A | |
| X | g.116172463C= | CA2453331713 | AGTR2 | c.183C= (p.Val61=) n.651C= | |
| X | g.116172463C>G | CA518449208 | AGTR2 | c.183C>G (p.Val61=) n.651C>G | gnomAD v4 |
| X | g.116172463C>T | CA518449207 | AGTR2 | c.183C>T (p.Val61=) n.651C>T | dbSNP |
| X | g.116172464A>C | CA414337775 | AGTR2 | c.184A>C (p.Asn62His) n.652A>C | |
| X | g.116172464A>G | CA414337776 | AGTR2 | c.184A>G (p.Asn62Asp) n.652A>G | |
| X | g.116172464A>T | CA414337777 | AGTR2 | c.184A>T (p.Asn62Tyr) n.652A>T | |
| X | g.116172465A>C | CA414337778 | AGTR2 | c.185A>C (p.Asn62Thr) n.653A>C | |
| X | g.116172465A>G | CA414337779 | AGTR2 | c.185A>G (p.Asn62Ser) n.653A>G | |
| X | g.116172465A>T | CA414337780 | AGTR2 | c.185A>T (p.Asn62Ile) n.653A>T | |
| X | g.116172466T>A | CA414337781 | AGTR2 | c.186T>A (p.Asn62Lys) n.654T>A | |
| X | g.116172466T>C | CA518449209 | AGTR2 | c.186T>C (p.Asn62=) n.654T>C | |
| X | g.116172466T>G | CA414337782 | AGTR2 | c.186T>G (p.Asn62Lys) n.654T>G | |
| X | g.116172466_116172467delinsTA | CA2453331714 | AGTR2 | c.186_187delinsTA (p.Asn62=) n.654_655delinsTA | |
| X | g.116172467del | CA10497241 | AGTR2 | c.187del (p.Ile63LeufsTer?) n.655del | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.116172467A>C | CA414337783 | AGTR2 | c.187A>C (p.Ile63Leu) n.655A>C | |
| X | g.116172467A>G | CA414337784 | AGTR2 | c.187A>G (p.Ile63Val) n.655A>G | |
| X | g.116172467A>T | CA414337785 | AGTR2 | c.187A>T (p.Ile63Phe) n.655A>T | |
| X | g.116172468T>A | CA414337788 | AGTR2 | c.188T>A (p.Ile63Asn) n.656T>A | |
| X | g.116172468T>C | CA414337786 | AGTR2 | c.188T>C (p.Ile63Thr) n.656T>C | |
| X | g.116172468T>G | CA414337789 | AGTR2 | c.188T>G (p.Ile63Ser) n.656T>G | |
| X | g.116172469T>A | CA518449210 | AGTR2 | c.189T>A (p.Ile63=) n.657T>A | |
| X | g.116172469T>C | CA518449211 | AGTR2 | c.189T>C (p.Ile63=) n.657T>C | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172469T>G | CA414337790 | AGTR2 | c.189T>G (p.Ile63Met) n.657T>G | |
| X | g.116172469T= | CA2453331716 | AGTR2 | c.189T= (p.Ile63=) n.657T= | |
| X | g.116172469_116172472delinsTGTC | CA2453331715 | AGTR2 | c.189_192delinsTGTC (p.Ile63=) n.657_660delinsTGTC | |
| X | g.116172470G>A | CA414337792 | AGTR2 | c.190G>A (p.Val64Ile) n.658G>A | |
| X | g.116172470G>C | CA414337791 | AGTR2 | c.190G>C (p.Val64Leu) n.658G>C | |
| X | g.116172470G>T | CA414337793 | AGTR2 | c.190G>T (p.Val64Phe) n.658G>T | |
| X | g.116172472_116172474del | CA644065608 | AGTR2 | c.192_194del (p.Val65del) n.660_662del | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172471T>A | CA414337794 | AGTR2 | c.191T>A (p.Val64Asp) n.659T>A | |
| X | g.116172471T>C | CA414337796 | AGTR2 | c.191T>C (p.Val64Ala) n.659T>C | |
| X | g.116172471T>G | CA414337795 | AGTR2 | c.191T>G (p.Val64Gly) n.659T>G | |
| X | g.116172472C>A | CA518449214 | AGTR2 | c.192C>A (p.Val64=) n.660C>A | |
| X | g.116172472C>G | CA518449212 | AGTR2 | c.192C>G (p.Val64=) n.660C>G | |
| X | g.116172472C>T | CA518449213 | AGTR2 | c.192C>T (p.Val64=) n.660C>T | gnomAD v4 |
| X | g.116172473G>A | CA414337797 | AGTR2 | c.193G>A (p.Val65Met) n.661G>A | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| X | g.116172473G>C | CA414337799 | AGTR2 | c.193G>C (p.Val65Leu) n.661G>C | gnomAD v4 |
| X | g.116172473G= | CA2453331717 | AGTR2 | c.193G= (p.Val65=) n.661G= | |
| X | g.116172473G>T | CA414337798 | AGTR2 | c.193G>T (p.Val65Leu) n.661G>T | |
| X | g.116172474T>A | CA414337800 | AGTR2 | c.194T>A (p.Val65Glu) n.662T>A | |
| X | g.116172474T>C | CA414337802 | AGTR2 | c.194T>C (p.Val65Ala) n.662T>C | |
| X | g.116172474T>G | CA414337801 | AGTR2 | c.194T>G (p.Val65Gly) n.662T>G | |
| X | g.116172475G>A | CA518449215 | AGTR2 | c.195G>A (p.Val65=) n.663G>A | |
| X | g.116172475G>C | CA518449216 | AGTR2 | c.195G>C (p.Val65=) n.663G>C | |
| X | g.116172475G>T | CA518449217 | AGTR2 | c.195G>T (p.Val65=) n.663G>T | gnomAD v4 |
| X | g.116172476G>A | CA414337803 | AGTR2 | c.196G>A (p.Val66Ile) n.664G>A | |
| X | g.116172476G>C | CA414337805 | AGTR2 | c.196G>C (p.Val66Leu) n.664G>C | |
| X | g.116172476G>T | CA414337804 | AGTR2 | c.196G>T (p.Val66Phe) n.664G>T | |
| X | g.116172477T>A | CA414337806 | AGTR2 | c.197T>A (p.Val66Asp) n.665T>A | |
| X | g.116172477T>C | CA414337808 | AGTR2 | c.197T>C (p.Val66Ala) n.665T>C | |
| X | g.116172477T>G | CA414337807 | AGTR2 | c.197T>G (p.Val66Gly) n.665T>G | |
| X | g.116172478T>A | CA518449218 | AGTR2 | c.198T>A (p.Val66=) n.666T>A | |
| X | g.116172478T>C | CA10497242 | AGTR2 | c.198T>C (p.Val66=) n.666T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.116172478T>G | CA518449219 | AGTR2 | c.198T>G (p.Val66=) n.666T>G | |
| X | g.116172478T= | CA2453331718 | AGTR2 | c.198T= (p.Val66=) n.666T= | |
| X | g.116172479A>C | CA414337809 | AGTR2 | c.199A>C (p.Thr67Pro) n.667A>C | |
| X | g.116172479A>G | CA414337810 | AGTR2 | c.199A>G (p.Thr67Ala) n.667A>G | |
| X | g.116172479A>T | CA414337811 | AGTR2 | c.199A>T (p.Thr67Ser) n.667A>T | |
| X | g.116172480C>A | CA414337812 | AGTR2 | c.200C>A (p.Thr67Lys) n.668C>A | |
| X | g.116172480C= | CA2453331719 | AGTR2 | c.200C= (p.Thr67=) n.668C= | |
| X | g.116172480C>G | CA414337813 | AGTR2 | c.200C>G (p.Thr67Arg) n.668C>G | |
| X | g.116172480C>T | CA414337814 | AGTR2 | c.200C>T (p.Thr67Ile) n.668C>T | dbSNP gnomAD v3 gnomAD v4 |
| X | g.116172481A= | CA2453331720 | AGTR2 | c.201A= (p.Thr67=) n.669A= | |
| X | g.116172481A>C | CA518449220 | AGTR2 | c.201A>C (p.Thr67=) n.669A>C | |
| X | g.116172481A>G | CA518449221 | AGTR2 | c.201A>G (p.Thr67=) n.669A>G | dbSNP gnomAD v3 gnomAD v4 |
| X | g.116172481A>T | CA518449222 | AGTR2 | c.201A>T (p.Thr67=) n.669A>T | |
| 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 |