| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.116172338T>A | CA414337500 | AGTR2 | c.58T>A (p.Phe20Ile) n.526T>A | gnomAD v4 |
| X | g.116172338T>C | CA414337501 | AGTR2 | c.58T>C (p.Phe20Leu) n.526T>C | |
| X | g.116172338T>G | CA414337502 | AGTR2 | c.58T>G (p.Phe20Val) n.526T>G | |
| X | g.116172339T>A | CA414337505 | AGTR2 | c.59T>A (p.Phe20Tyr) n.527T>A | |
| X | g.116172339T>C | CA414337504 | AGTR2 | c.59T>C (p.Phe20Ser) n.527T>C | |
| X | g.116172339T>G | CA414337503 | AGTR2 | c.59T>G (p.Phe20Cys) n.527T>G | |
| X | g.116172340C>A | CA334723676 | AGTR2 | c.60C>A (p.Phe20Leu) n.528C>A | dbSNP gnomAD v4 |
| X | g.116172340C= | CA2453331668 | AGTR2 | c.60C= (p.Phe20=) n.528C= | |
| X | g.116172340C>G | CA10497224 | AGTR2 | c.60C>G (p.Phe20Leu) n.528C>G | dbSNP ExAC gnomAD v2 |
| X | g.116172340C>T | CA10497225 | AGTR2 | c.60C>T (p.Phe20=) n.528C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.116172341G>A | CA16621185 | AGTR2 | c.61G>A (p.Gly21Arg) n.529G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| X | g.116172341G>C | CA414337507 | AGTR2 | c.61G>C (p.Gly21Arg) n.529G>C | gnomAD v4 |
| X | g.116172341G= | CA2453331669 | AGTR2 | c.61G= (p.Gly21=) n.529G= | |
| X | g.116172341G>T | CA414337508 | AGTR2 | c.61G>T (p.Gly21Trp) n.529G>T | |
| X | g.116172342G>A | CA414337509 | AGTR2 | c.62G>A (p.Gly21Glu) n.530G>A | |
| X | g.116172342G>C | CA414337510 | AGTR2 | c.62G>C (p.Gly21Ala) n.530G>C | |
| X | g.116172342G= | CA2453331670 | AGTR2 | c.62G= (p.Gly21=) n.530G= | |
| X | g.116172342G>T | CA151691 | AGTR2 | c.62G>T (p.Gly21Val) n.530G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172343G>A | CA518449131 | AGTR2 | c.63G>A (p.Gly21=) n.531G>A | dbSNP |
| X | g.116172343G>C | CA518449130 | AGTR2 | c.63G>C (p.Gly21=) n.531G>C | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172343G= | CA2453331671 | AGTR2 | c.63G= (p.Gly21=) n.531G= | |
| X | g.116172343G>T | CA518449129 | AGTR2 | c.63G>T (p.Gly21=) n.531G>T | |
| X | g.116172344C>A | CA414337511 | AGTR2 | c.64C>A (p.Leu22Ile) n.532C>A | |
| X | g.116172344C>G | CA414337512 | AGTR2 | c.64C>G (p.Leu22Val) n.532C>G | |
| X | g.116172344C>T | CA414337513 | AGTR2 | c.64C>T (p.Leu22Phe) n.532C>T | |
| X | g.116172345T>A | CA414337516 | AGTR2 | c.65T>A (p.Leu22His) n.533T>A | |
| X | g.116172345T>C | CA414337515 | AGTR2 | c.65T>C (p.Leu22Pro) n.533T>C | dbSNP |
| X | g.116172345T>G | CA414337514 | AGTR2 | c.65T>G (p.Leu22Arg) n.533T>G | |
| X | g.116172345T= | CA2453331672 | AGTR2 | c.65T= (p.Leu22=) n.533T= | |
| X | g.116172346T>A | CA518449132 | AGTR2 | c.66T>A (p.Leu22=) n.534T>A | |
| X | g.116172346T>C | CA518449133 | AGTR2 | c.66T>C (p.Leu22=) n.534T>C | |
| X | g.116172346T>G | CA518449134 | AGTR2 | c.66T>G (p.Leu22=) n.534T>G | |
| X | g.116172347G>A | CA334723677 | AGTR2 | c.67G>A (p.Val23Met) n.535G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172347G>C | CA414337517 | AGTR2 | c.67G>C (p.Val23Leu) n.535G>C | |
| X | g.116172347G= | CA2453331673 | AGTR2 | c.67G= (p.Val23=) n.535G= | |
| X | g.116172347G>T | CA414337518 | AGTR2 | c.67G>T (p.Val23Leu) n.535G>T | |
| X | g.116172348T>A | CA414337519 | AGTR2 | c.68T>A (p.Val23Glu) n.536T>A | |
| X | g.116172348T>C | CA414337521 | AGTR2 | c.68T>C (p.Val23Ala) n.536T>C | |
| X | g.116172348T>G | CA414337522 | AGTR2 | c.68T>G (p.Val23Gly) n.536T>G | |
| X | g.116172349G>A | CA518449135 | AGTR2 | c.69G>A (p.Val23=) n.537G>A | |
| X | g.116172349G>C | CA518449136 | AGTR2 | c.69G>C (p.Val23=) n.537G>C | |
| X | g.116172349G>T | CA518449137 | AGTR2 | c.69G>T (p.Val23=) n.537G>T | |
| X | g.116172350A>C | CA414337525 | AGTR2 | c.70A>C (p.Asn24His) n.538A>C | |
| X | g.116172350A>G | CA414337523 | AGTR2 | c.70A>G (p.Asn24Asp) n.538A>G | |
| X | g.116172350A>T | CA414337524 | AGTR2 | c.70A>T (p.Asn24Tyr) n.538A>T | |
| X | g.116172351A>C | CA414337528 | AGTR2 | c.71A>C (p.Asn24Thr) n.539A>C | |
| X | g.116172351A>G | CA414337529 | AGTR2 | c.71A>G (p.Asn24Ser) n.539A>G | |
| X | g.116172351A>T | CA414337530 | AGTR2 | c.71A>T (p.Asn24Ile) n.539A>T | |
| X | g.116172352C>A | CA414337531 | AGTR2 | c.72C>A (p.Asn24Lys) n.540C>A | |
| X | g.116172352C>G | CA414337532 | AGTR2 | c.72C>G (p.Asn24Lys) n.540C>G | |
| X | g.116172352C>T | CA518449138 | AGTR2 | c.72C>T (p.Asn24=) n.540C>T | gnomAD v4 |
| X | g.116172353A>C | CA414337533 | AGTR2 | c.73A>C (p.Ile25Leu) n.541A>C | |
| X | g.116172353A>G | CA414337535 | AGTR2 | c.73A>G (p.Ile25Val) n.541A>G | |
| X | g.116172353A>T | CA414337534 | AGTR2 | c.73A>T (p.Ile25Phe) n.541A>T | |
| X | g.116172354T>A | CA414337536 | AGTR2 | c.74T>A (p.Ile25Asn) n.542T>A | gnomAD v4 |
| X | g.116172354T>C | CA414337537 | AGTR2 | c.74T>C (p.Ile25Thr) n.542T>C | |
| X | g.116172354T>G | CA414337538 | AGTR2 | c.74T>G (p.Ile25Ser) n.542T>G | |
| X | g.116172355C>A | CA518449139 | AGTR2 | c.75C>A (p.Ile25=) n.543C>A | |
| X | g.116172355C>G | CA414337539 | AGTR2 | c.75C>G (p.Ile25Met) n.543C>G | |
| X | g.116172355C>T | CA518449140 | AGTR2 | c.75C>T (p.Ile25=) n.543C>T | |
| X | g.116172356T>A | CA414337540 | AGTR2 | c.76T>A (p.Ser26Thr) n.544T>A | |
| X | g.116172356T>C | CA414337541 | AGTR2 | c.76T>C (p.Ser26Pro) n.544T>C | ClinVar |
| X | g.116172356T>G | CA414337542 | AGTR2 | c.76T>G (p.Ser26Ala) n.544T>G | |
| X | g.116172357C>A | CA414337543 | AGTR2 | c.77C>A (p.Ser26Tyr) n.545C>A | |
| X | g.116172357C>G | CA414337544 | AGTR2 | c.77C>G (p.Ser26Cys) n.545C>G | |
| X | g.116172357C>T | CA414337545 | AGTR2 | c.77C>T (p.Ser26Phe) n.545C>T | |
| X | g.116172358T>A | CA518449141 | AGTR2 | c.78T>A (p.Ser26=) n.546T>A | |
| X | g.116172358T>C | CA518449142 | AGTR2 | c.78T>C (p.Ser26=) n.546T>C | gnomAD v4 |
| X | g.116172358T>G | CA518449143 | AGTR2 | c.78T>G (p.Ser26=) n.546T>G | |
| X | g.116172359G>A | CA414337548 | AGTR2 | c.79G>A (p.Gly27Ser) n.547G>A | dbSNP gnomAD v2 |
| X | g.116172359G>C | CA414337547 | AGTR2 | c.79G>C (p.Gly27Arg) n.547G>C | |
| X | g.116172359G= | CA2453331674 | AGTR2 | c.79G= (p.Gly27=) n.547G= | |
| X | g.116172359G>T | CA414337546 | AGTR2 | c.79G>T (p.Gly27Cys) n.547G>T | |
| X | g.116172360G>A | CA414337549 | AGTR2 | c.80G>A (p.Gly27Asp) n.548G>A | |
| X | g.116172360G>C | CA414337551 | AGTR2 | c.80G>C (p.Gly27Ala) n.548G>C | gnomAD v4 |
| X | g.116172360G>T | CA414337550 | AGTR2 | c.80G>T (p.Gly27Val) n.548G>T | |
| X | g.116172361C>A | CA518449144 | AGTR2 | c.81C>A (p.Gly27=) n.549C>A | |
| X | g.116172361C>G | CA518449145 | AGTR2 | c.81C>G (p.Gly27=) n.549C>G | |
| X | g.116172361C>T | CA518449146 | AGTR2 | c.81C>T (p.Gly27=) n.549C>T | |
| X | g.116172364_116172366del | CA2556362418 | AGTR2 | c.84_86del (p.Asn29del) n.552_554del | |
| X | g.116172362A>C | CA414337552 | AGTR2 | c.82A>C (p.Asn28His) n.550A>C | |
| X | g.116172362A>G | CA414337554 | AGTR2 | c.82A>G (p.Asn28Asp) n.550A>G | |
| X | g.116172362A>T | CA414337553 | AGTR2 | c.82A>T (p.Asn28Tyr) n.550A>T | |
| X | g.116172363A= | CA2453331675 | AGTR2 | c.83A= (p.Asn28=) n.551A= | |
| X | g.116172363A>C | CA414337555 | AGTR2 | c.83A>C (p.Asn28Thr) n.551A>C | |
| X | g.116172363A>G | CA334723678 | AGTR2 | c.83A>G (p.Asn28Ser) n.551A>G | dbSNP |
| X | g.116172363A>T | CA414337556 | AGTR2 | c.83A>T (p.Asn28Ile) n.551A>T | gnomAD v4 |
| X | g.116172364C>A | CA414337557 | AGTR2 | c.84C>A (p.Asn28Lys) n.552C>A | |
| X | g.116172364C>G | CA414337558 | AGTR2 | c.84C>G (p.Asn28Lys) n.552C>G | |
| X | g.116172364C>T | CA518449147 | AGTR2 | c.84C>T (p.Asn28=) n.552C>T | |
| X | g.116172365A>C | CA414337559 | AGTR2 | c.85A>C (p.Asn29His) n.553A>C | |
| X | g.116172365A>G | CA414337560 | AGTR2 | c.85A>G (p.Asn29Asp) n.553A>G | |
| X | g.116172365A>T | CA414337561 | AGTR2 | c.85A>T (p.Asn29Tyr) n.553A>T | |
| X | g.116172365_116172367del | CA2694510859 | AGTR2 | c.85_87del (p.Asn29del) n.553_555del | gnomAD v4 |
| X | g.116172366A= | CA2453331676 | AGTR2 | c.86A= (p.Asn29=) n.554A= | |
| X | g.116172366A>C | CA414337562 | AGTR2 | c.86A>C (p.Asn29Thr) n.554A>C | |
| X | g.116172366A>G | CA10497226 | AGTR2 | c.86A>G (p.Asn29Ser) n.554A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172366A>T | CA414337563 | AGTR2 | c.86A>T (p.Asn29Ile) n.554A>T | |
| X | g.116172367T>A | CA414337564 | AGTR2 | c.87T>A (p.Asn29Lys) n.555T>A | |
| X | g.116172367T>C | CA518449148 | AGTR2 | c.87T>C (p.Asn29=) n.555T>C | dbSNP gnomAD v4 |
| X | g.116172367T>G | CA414337565 | AGTR2 | c.87T>G (p.Asn29Lys) n.555T>G | gnomAD v4 |
| X | g.116172367T= | CA2453331677 | AGTR2 | c.87T= (p.Asn29=) n.555T= | |
| X | g.116172368G>A | CA414337568 | AGTR2 | c.88G>A (p.Glu30Lys) n.556G>A | |
| X | g.116172368G>C | CA414337567 | AGTR2 | c.88G>C (p.Glu30Gln) n.556G>C | |
| X | g.116172368G>T | CA414337566 | AGTR2 | c.88G>T (p.Glu30Ter) n.556G>T | gnomAD v4 |
| X | g.116172369A>C | CA414337569 | AGTR2 | c.89A>C (p.Glu30Ala) n.557A>C | |
| X | g.116172369A>G | CA414337570 | AGTR2 | c.89A>G (p.Glu30Gly) n.557A>G | |
| X | g.116172369A>T | CA414337571 | AGTR2 | c.89A>T (p.Glu30Val) n.557A>T | |
| X | g.116172370G>A | CA518449149 | AGTR2 | c.90G>A (p.Glu30=) n.558G>A | dbSNP gnomAD v4 |
| X | g.116172370G>C | CA414337572 | AGTR2 | c.90G>C (p.Glu30Asp) n.558G>C | ClinVar |
| X | g.116172370G= | CA2453331678 | AGTR2 | c.90G= (p.Glu30=) n.558G= | |
| X | g.116172370G>T | CA414337573 | AGTR2 | c.90G>T (p.Glu30Asp) n.558G>T | |
| X | g.116172371T>A | CA414337574 | AGTR2 | c.91T>A (p.Ser31Thr) n.559T>A | |
| X | g.116172371T>C | CA414337575 | AGTR2 | c.91T>C (p.Ser31Pro) n.559T>C | |
| X | g.116172371T>G | CA414337576 | AGTR2 | c.91T>G (p.Ser31Ala) n.559T>G | COSMIC |
| X | g.116172372C>A | CA414337577 | AGTR2 | c.92C>A (p.Ser31Tyr) n.560C>A | COSMIC |
| X | g.116172372C>G | CA414337578 | AGTR2 | c.92C>G (p.Ser31Cys) n.560C>G | |
| X | g.116172372C>T | CA414337579 | AGTR2 | c.92C>T (p.Ser31Phe) n.560C>T | |
| X | g.116172373T>A | CA518449150 | AGTR2 | c.93T>A (p.Ser31=) n.561T>A | |
| X | g.116172373T>C | CA518449152 | AGTR2 | c.93T>C (p.Ser31=) n.561T>C | |
| X | g.116172373T>G | CA518449151 | AGTR2 | c.93T>G (p.Ser31=) n.561T>G | |
| X | g.116172374A= | CA2453331679 | AGTR2 | c.94A= (p.Thr32=) n.562A= | |
| X | g.116172374A>C | CA414337581 | AGTR2 | c.94A>C (p.Thr32Pro) n.562A>C | |
| X | g.116172374A>G | CA414337582 | AGTR2 | c.94A>G (p.Thr32Ala) n.562A>G | dbSNP |
| X | g.116172374A>T | CA414337580 | AGTR2 | c.94A>T (p.Thr32Ser) n.562A>T | |
| X | g.116172375C>A | CA414337583 | AGTR2 | c.95C>A (p.Thr32Asn) n.563C>A | |
| X | g.116172375C>G | CA414337584 | AGTR2 | c.95C>G (p.Thr32Ser) n.563C>G | |
| X | g.116172375C>T | CA414337585 | AGTR2 | c.95C>T (p.Thr32Ile) n.563C>T | |
| X | g.116172376C>A | CA518449153 | AGTR2 | c.96C>A (p.Thr32=) n.564C>A | gnomAD v4 |
| X | g.116172376C>G | CA518449154 | AGTR2 | c.96C>G (p.Thr32=) n.564C>G | |
| X | g.116172376C>T | CA518449155 | AGTR2 | c.96C>T (p.Thr32=) n.564C>T | |
| X | g.116172377T>A | CA414337586 | AGTR2 | c.97T>A (p.Leu33Met) n.565T>A | |
| X | g.116172377T>C | CA10497228 | AGTR2 | c.97T>C (p.Leu33=) n.565T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.116172377T>G | CA10497227 | AGTR2 | c.97T>G (p.Leu33Val) n.565T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172377T= | CA2453331680 | AGTR2 | c.97T= (p.Leu33=) n.565T= | |
| X | g.116172378T>A | CA414337587 | AGTR2 | c.98T>A (p.Leu33Ter) n.566T>A | |
| X | g.116172378T>C | CA414337588 | AGTR2 | c.98T>C (p.Leu33Ser) n.566T>C | |
| X | g.116172378T>G | CA414337589 | AGTR2 | c.98T>G (p.Leu33Trp) n.566T>G | |
| X | g.116172379G>A | CA518449156 | AGTR2 | c.99G>A (p.Leu33=) n.567G>A | dbSNP gnomAD v4 COSMIC |
| X | g.116172379G>C | CA414337590 | AGTR2 | c.99G>C (p.Leu33Phe) n.567G>C | |
| X | g.116172379G= | CA2453331681 | AGTR2 | c.99G= (p.Leu33=) n.567G= | |
| X | g.116172379G>T | CA414337591 | AGTR2 | c.99G>T (p.Leu33Phe) n.567G>T | |
| X | g.116172380A>C | CA414337593 | AGTR2 | c.100A>C (p.Asn34His) n.568A>C | |
| X | g.116172380A>G | CA414337594 | AGTR2 | c.100A>G (p.Asn34Asp) n.568A>G | |
| X | g.116172380A>T | CA414337592 | AGTR2 | c.100A>T (p.Asn34Tyr) n.568A>T | |
| X | g.116172381A>C | CA414337595 | AGTR2 | c.101A>C (p.Asn34Thr) n.569A>C | |
| X | g.116172381A>G | CA414337596 | AGTR2 | c.101A>G (p.Asn34Ser) n.569A>G | |
| X | g.116172381A>T | CA414337597 | AGTR2 | c.101A>T (p.Asn34Ile) n.569A>T | |
| X | g.116172382C>A | CA414337598 | AGTR2 | c.102C>A (p.Asn34Lys) n.570C>A | |
| X | g.116172382C>G | CA414337599 | AGTR2 | c.102C>G (p.Asn34Lys) n.570C>G | |
| X | g.116172382C>T | CA518449157 | AGTR2 | c.102C>T (p.Asn34=) n.570C>T | |
| X | g.116172383T>A | CA414337602 | AGTR2 | c.103T>A (p.Cys35Ser) n.571T>A | |
| X | g.116172383T>C | CA414337600 | AGTR2 | c.103T>C (p.Cys35Arg) n.571T>C | dbSNP gnomAD v2 |
| X | g.116172383T>G | CA414337601 | AGTR2 | c.103T>G (p.Cys35Gly) n.571T>G | |
| X | g.116172383T= | CA2453331682 | AGTR2 | c.103T= (p.Cys35=) n.571T= | |
| X | g.116172384G>A | CA414337603 | AGTR2 | c.104G>A (p.Cys35Tyr) n.572G>A | |
| X | g.116172384G>C | CA414337604 | AGTR2 | c.104G>C (p.Cys35Ser) n.572G>C | |
| X | g.116172384G>T | CA414337605 | AGTR2 | c.104G>T (p.Cys35Phe) n.572G>T | |
| X | g.116172385T>A | CA414337606 | AGTR2 | c.105T>A (p.Cys35Ter) n.573T>A | |
| X | g.116172385T>C | CA518449158 | AGTR2 | c.105T>C (p.Cys35=) n.573T>C | |
| X | g.116172385T>G | CA414337607 | AGTR2 | c.105T>G (p.Cys35Trp) n.573T>G | |
| X | g.116172386T>A | CA414337610 | AGTR2 | c.106T>A (p.Ser36Thr) n.574T>A | |
| X | g.116172386T>C | CA414337609 | AGTR2 | c.106T>C (p.Ser36Pro) n.574T>C | dbSNP gnomAD v2 |
| X | g.116172386T>G | CA414337608 | AGTR2 | c.106T>G (p.Ser36Ala) n.574T>G | |
| X | g.116172386T= | CA2453331683 | AGTR2 | c.106T= (p.Ser36=) n.574T= | |
| X | g.116172387C>A | CA414337611 | AGTR2 | c.107C>A (p.Ser36Ter) n.575C>A | COSMIC |
| X | g.116172387C>G | CA414337613 | AGTR2 | c.107C>G (p.Ser36Ter) n.575C>G | |
| X | g.116172387C>T | CA414337612 | AGTR2 | c.107C>T (p.Ser36Leu) n.575C>T | |
| X | g.116172388A= | CA2453331684 | AGTR2 | c.108A= (p.Ser36=) n.576A= | |
| X | g.116172388A>C | CA518449159 | AGTR2 | c.108A>C (p.Ser36=) n.576A>C | |
| X | g.116172388A>G | CA518449160 | AGTR2 | c.108A>G (p.Ser36=) n.576A>G | dbSNP |
| X | g.116172388A>T | CA518449161 | AGTR2 | c.108A>T (p.Ser36=) n.576A>T | |
| 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= |