| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.116172299C>A | CA414337410 | AGTR2 | c.19C>A (p.Leu7Ile) n.487C>A | gnomAD v4 |
| X | g.116172299C>G | CA414337411 | AGTR2 | c.19C>G (p.Leu7Val) n.487C>G | |
| X | g.116172299C>T | CA414337412 | AGTR2 | c.19C>T (p.Leu7Phe) n.487C>T | |
| X | g.116172300T>A | CA414337413 | AGTR2 | c.20T>A (p.Leu7His) n.488T>A | |
| X | g.116172300T>C | CA414337414 | AGTR2 | c.20T>C (p.Leu7Pro) n.488T>C | |
| X | g.116172300T>G | CA414337415 | AGTR2 | c.20T>G (p.Leu7Arg) n.488T>G | |
| X | g.116172301T>A | CA518449102 | AGTR2 | c.21T>A (p.Leu7=) n.489T>A | |
| X | g.116172301T>C | CA518449103 | AGTR2 | c.21T>C (p.Leu7=) n.489T>C | |
| X | g.116172301T>G | CA10497223 | AGTR2 | c.21T>G (p.Leu7=) n.489T>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.116172301T= | CA2453331658 | AGTR2 | c.21T= (p.Leu7=) n.489T= | |
| X | g.116172302G>A | CA414337416 | AGTR2 | c.22G>A (p.Ala8Thr) n.490G>A | gnomAD v4 |
| X | g.116172302G>C | CA414337417 | AGTR2 | c.22G>C (p.Ala8Pro) n.490G>C | |
| X | g.116172302G>T | CA414337418 | AGTR2 | c.22G>T (p.Ala8Ser) n.490G>T | |
| X | g.116172303C>A | CA414337419 | AGTR2 | c.23C>A (p.Ala8Asp) n.491C>A | |
| X | g.116172303C= | CA2453331659 | AGTR2 | c.23C= (p.Ala8=) n.491C= | |
| X | g.116172303C>G | CA414337420 | AGTR2 | c.23C>G (p.Ala8Gly) n.491C>G | |
| X | g.116172303C>T | CA414337421 | AGTR2 | c.23C>T (p.Ala8Val) n.491C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| X | g.116172304C>A | CA518449104 | AGTR2 | c.24C>A (p.Ala8=) n.492C>A | |
| X | g.116172304C>G | CA518449105 | AGTR2 | c.24C>G (p.Ala8=) n.492C>G | |
| X | g.116172304C>T | CA518449106 | AGTR2 | c.24C>T (p.Ala8=) n.492C>T | |
| X | g.116172305A>C | CA414337422 | AGTR2 | c.25A>C (p.Thr9Pro) n.493A>C | |
| X | g.116172305A>G | CA414337424 | AGTR2 | c.25A>G (p.Thr9Ala) n.493A>G | |
| X | g.116172305A>T | CA414337423 | AGTR2 | c.25A>T (p.Thr9Ser) n.493A>T | |
| X | g.116172306C>A | CA414337425 | AGTR2 | c.26C>A (p.Thr9Asn) n.494C>A | gnomAD v4 |
| X | g.116172306C>G | CA414337427 | AGTR2 | c.26C>G (p.Thr9Ser) n.494C>G | |
| X | g.116172306C>T | CA414337426 | AGTR2 | c.26C>T (p.Thr9Ile) n.494C>T | |
| X | g.116172307T>A | CA518449107 | AGTR2 | c.27T>A (p.Thr9=) n.495T>A | |
| X | g.116172307T>C | CA518449109 | AGTR2 | c.27T>C (p.Thr9=) n.495T>C | |
| X | g.116172307T>G | CA518449108 | AGTR2 | c.27T>G (p.Thr9=) n.495T>G | |
| X | g.116172308A>C | CA414337428 | AGTR2 | c.28A>C (p.Thr10Pro) n.496A>C | |
| X | g.116172308A>G | CA414337430 | AGTR2 | c.28A>G (p.Thr10Ala) n.496A>G | |
| X | g.116172308A>T | CA414337429 | AGTR2 | c.28A>T (p.Thr10Ser) n.496A>T | |
| X | g.116172309C>A | CA414337431 | AGTR2 | c.29C>A (p.Thr10Asn) n.497C>A | COSMIC |
| X | g.116172309C= | CA2453331660 | AGTR2 | c.29C= (p.Thr10=) n.497C= | |
| X | g.116172309C>G | CA414337432 | AGTR2 | c.29C>G (p.Thr10Ser) n.497C>G | |
| X | g.116172309C>T | CA414337433 | AGTR2 | c.29C>T (p.Thr10Ile) n.497C>T | dbSNP gnomAD v4 |
| X | g.116172310T>A | CA518449110 | AGTR2 | c.30T>A (p.Thr10=) n.498T>A | |
| X | g.116172310T>C | CA518449111 | AGTR2 | c.30T>C (p.Thr10=) n.498T>C | |
| X | g.116172310T>G | CA518449112 | AGTR2 | c.30T>G (p.Thr10=) n.498T>G | |
| X | g.116172311A>C | CA414337434 | AGTR2 | c.31A>C (p.Ser11Arg) n.499A>C | |
| X | g.116172311A>G | CA414337435 | AGTR2 | c.31A>G (p.Ser11Gly) n.499A>G | |
| X | g.116172311A>T | CA414337436 | AGTR2 | c.31A>T (p.Ser11Cys) n.499A>T | |
| X | g.116172312G>A | CA414337437 | AGTR2 | c.32G>A (p.Ser11Asn) n.500G>A | dbSNP gnomAD v2 |
| X | g.116172312G>C | CA414337438 | AGTR2 | c.32G>C (p.Ser11Thr) n.500G>C | |
| X | g.116172312G= | CA2453331661 | AGTR2 | c.32G= (p.Ser11=) n.500G= | |
| X | g.116172312G>T | CA414337439 | AGTR2 | c.32G>T (p.Ser11Ile) n.500G>T | |
| X | g.116172313C>A | CA414337440 | AGTR2 | c.33C>A (p.Ser11Arg) n.501C>A | |
| X | g.116172313C>G | CA414337441 | AGTR2 | c.33C>G (p.Ser11Arg) n.501C>G | |
| X | g.116172313C>T | CA518449113 | AGTR2 | c.33C>T (p.Ser11=) n.501C>T | gnomAD v4 |
| X | g.116172314A>C | CA414337444 | AGTR2 | c.34A>C (p.Lys12Gln) n.502A>C | |
| X | g.116172314A>G | CA414337442 | AGTR2 | c.34A>G (p.Lys12Glu) n.502A>G | gnomAD v4 |
| X | g.116172314A>T | CA414337443 | AGTR2 | c.34A>T (p.Lys12Ter) n.502A>T | |
| X | g.116172315A>C | CA414337445 | AGTR2 | c.35A>C (p.Lys12Thr) n.503A>C | |
| X | g.116172315A>G | CA414337446 | AGTR2 | c.35A>G (p.Lys12Arg) n.503A>G | |
| X | g.116172315A>T | CA414337447 | AGTR2 | c.35A>T (p.Lys12Ile) n.503A>T | |
| X | g.116172316A>C | CA414337448 | AGTR2 | c.36A>C (p.Lys12Asn) n.504A>C | |
| X | g.116172316A>G | CA518449114 | AGTR2 | c.36A>G (p.Lys12=) n.504A>G | |
| X | g.116172316A>T | CA414337449 | AGTR2 | c.36A>T (p.Lys12Asn) n.504A>T | |
| X | g.116172317A>C | CA414337450 | AGTR2 | c.37A>C (p.Asn13His) n.505A>C | |
| X | g.116172317A>G | CA414337451 | AGTR2 | c.37A>G (p.Asn13Asp) n.505A>G | |
| X | g.116172317A>T | CA414337452 | AGTR2 | c.37A>T (p.Asn13Tyr) n.505A>T | |
| X | g.116172317_116172318insCCACCCCAAACACACCCAAC | CA2823125652 | AGTR2 | c.37_38insCCACCCCAAACACACCCAAC (p.Asn13ThrfsTer18) n.505_506insCCACCCCAAACACACCCAAC | |
| X | g.116172318A>C | CA414337453 | AGTR2 | c.38A>C (p.Asn13Thr) n.506A>C | |
| X | g.116172318A>G | CA414337454 | AGTR2 | c.38A>G (p.Asn13Ser) n.506A>G | |
| X | g.116172318A>T | CA414337455 | AGTR2 | c.38A>T (p.Asn13Ile) n.506A>T | |
| X | g.116172319C>A | CA414337457 | AGTR2 | c.39C>A (p.Asn13Lys) n.507C>A | |
| X | g.116172319C>G | CA414337456 | AGTR2 | c.39C>G (p.Asn13Lys) n.507C>G | |
| X | g.116172319C>T | CA518449115 | AGTR2 | c.39C>T (p.Asn13=) n.507C>T | |
| X | g.116172320A>C | CA414337458 | AGTR2 | c.40A>C (p.Ile14Leu) n.508A>C | |
| X | g.116172320A>G | CA414337459 | AGTR2 | c.40A>G (p.Ile14Val) n.508A>G | |
| X | g.116172320A>T | CA414337460 | AGTR2 | c.40A>T (p.Ile14Phe) n.508A>T | |
| X | g.116172321T>A | CA414337461 | AGTR2 | c.41T>A (p.Ile14Asn) n.509T>A | |
| X | g.116172321T>C | CA414337462 | AGTR2 | c.41T>C (p.Ile14Thr) n.509T>C | dbSNP gnomAD v4 |
| X | g.116172321T>G | CA414337463 | AGTR2 | c.41T>G (p.Ile14Ser) n.509T>G | |
| X | g.116172321T= | CA2453331662 | AGTR2 | c.41T= (p.Ile14=) n.509T= | |
| X | g.116172322T>A | CA518449117 | AGTR2 | c.42T>A (p.Ile14=) n.510T>A | |
| X | g.116172322T>C | CA518449116 | AGTR2 | c.42T>C (p.Ile14=) n.510T>C | gnomAD v4 |
| X | g.116172322T>G | CA414337464 | AGTR2 | c.42T>G (p.Ile14Met) n.510T>G | |
| X | g.116172323A>C | CA414337465 | AGTR2 | c.43A>C (p.Thr15Pro) n.511A>C | |
| X | g.116172323A>G | CA414337466 | AGTR2 | c.43A>G (p.Thr15Ala) n.511A>G | |
| X | g.116172323A>T | CA414337467 | AGTR2 | c.43A>T (p.Thr15Ser) n.511A>T | |
| X | g.116172324C>A | CA414337468 | AGTR2 | c.44C>A (p.Thr15Asn) n.512C>A | gnomAD v4 |
| X | g.116172324C>G | CA414337469 | AGTR2 | c.44C>G (p.Thr15Ser) n.512C>G | |
| X | g.116172324C>T | CA414337470 | AGTR2 | c.44C>T (p.Thr15Ile) n.512C>T | |
| X | g.116172325C>A | CA518449118 | AGTR2 | c.45C>A (p.Thr15=) n.513C>A | |
| X | g.116172325C>G | CA518449119 | AGTR2 | c.45C>G (p.Thr15=) n.513C>G | |
| X | g.116172325C>T | CA518449120 | AGTR2 | c.45C>T (p.Thr15=) n.513C>T | |
| X | g.116172326A= | CA2453331663 | AGTR2 | c.46A= (p.Ser16=) n.514A= | |
| X | g.116172326A>C | CA414337473 | AGTR2 | c.46A>C (p.Ser16Arg) n.514A>C | |
| X | g.116172326A>G | CA414337471 | AGTR2 | c.46A>G (p.Ser16Gly) n.514A>G | |
| X | g.116172326A>T | CA414337472 | AGTR2 | c.46A>T (p.Ser16Cys) n.514A>T | dbSNP |
| X | g.116172327G>A | CA414337474 | AGTR2 | c.47G>A (p.Ser16Asn) n.515G>A | |
| X | g.116172327G>C | CA414337475 | AGTR2 | c.47G>C (p.Ser16Thr) n.515G>C | |
| X | g.116172327G>T | CA414337476 | AGTR2 | c.47G>T (p.Ser16Ile) n.515G>T | |
| X | g.116172328C>A | CA414337477 | AGTR2 | c.48C>A (p.Ser16Arg) n.516C>A | |
| X | g.116172328C= | CA2453331664 | AGTR2 | c.48C= (p.Ser16=) n.516C= | |
| X | g.116172328C>G | CA414337478 | AGTR2 | c.48C>G (p.Ser16Arg) n.516C>G | |
| X | g.116172328C>T | CA518449121 | AGTR2 | c.48C>T (p.Ser16=) n.516C>T | dbSNP gnomAD v4 |
| X | g.116172329G>A | CA414337479 | AGTR2 | c.49G>A (p.Gly17Ser) n.517G>A | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172329G>C | CA414337480 | AGTR2 | c.49G>C (p.Gly17Arg) n.517G>C | |
| X | g.116172329G= | CA2453331665 | AGTR2 | c.49G= (p.Gly17=) n.517G= | |
| X | g.116172329G>T | CA414337481 | AGTR2 | c.49G>T (p.Gly17Cys) n.517G>T | dbSNP gnomAD v3 gnomAD v4 |
| X | g.116172330G>A | CA414337482 | AGTR2 | c.50G>A (p.Gly17Asp) n.518G>A | |
| X | g.116172330G>C | CA414337483 | AGTR2 | c.50G>C (p.Gly17Ala) n.518G>C | |
| X | g.116172330G>T | CA414337484 | AGTR2 | c.50G>T (p.Gly17Val) n.518G>T | |
| X | g.116172331T>A | CA518449122 | AGTR2 | c.51T>A (p.Gly17=) n.519T>A | |
| X | g.116172331T>C | CA518449123 | AGTR2 | c.51T>C (p.Gly17=) n.519T>C | |
| X | g.116172331T>G | CA518449124 | AGTR2 | c.51T>G (p.Gly17=) n.519T>G | |
| X | g.116172332C>A | CA414337487 | AGTR2 | c.52C>A (p.Leu18Ile) n.520C>A | |
| X | g.116172332C= | CA2453331666 | AGTR2 | c.52C= (p.Leu18=) n.520C= | |
| X | g.116172332C>G | CA414337486 | AGTR2 | c.52C>G (p.Leu18Val) n.520C>G | |
| X | g.116172332C>T | CA414337485 | AGTR2 | c.52C>T (p.Leu18Phe) n.520C>T | dbSNP |
| X | g.116172333T>A | CA414337488 | AGTR2 | c.53T>A (p.Leu18His) n.521T>A | |
| X | g.116172333T>C | CA414337490 | AGTR2 | c.53T>C (p.Leu18Pro) n.521T>C | |
| X | g.116172333T>G | CA414337489 | AGTR2 | c.53T>G (p.Leu18Arg) n.521T>G | |
| X | g.116172334T>A | CA518449125 | AGTR2 | c.54T>A (p.Leu18=) n.522T>A | |
| X | g.116172334T>C | CA518449126 | AGTR2 | c.54T>C (p.Leu18=) n.522T>C | |
| X | g.116172334T>G | CA518449127 | AGTR2 | c.54T>G (p.Leu18=) n.522T>G | COSMIC |
| X | g.116172335C>A | CA414337491 | AGTR2 | c.55C>A (p.His19Asn) n.523C>A | gnomAD v4 |
| X | g.116172335C>G | CA414337492 | AGTR2 | c.55C>G (p.His19Asp) n.523C>G | |
| X | g.116172335C>T | CA414337493 | AGTR2 | c.55C>T (p.His19Tyr) n.523C>T | COSMIC |
| X | g.116172336A>C | CA414337494 | AGTR2 | c.56A>C (p.His19Pro) n.524A>C | |
| X | g.116172336A>G | CA414337496 | AGTR2 | c.56A>G (p.His19Arg) n.524A>G | |
| X | g.116172336A>T | CA414337497 | AGTR2 | c.56A>T (p.His19Leu) n.524A>T | |
| X | g.116172337C>A | CA414337498 | AGTR2 | c.57C>A (p.His19Gln) n.525C>A | dbSNP |
| X | g.116172337C= | CA2453331667 | AGTR2 | c.57C= (p.His19=) n.525C= | |
| X | g.116172337C>G | CA414337499 | AGTR2 | c.57C>G (p.His19Gln) n.525C>G | |
| X | g.116172337C>T | CA518449128 | AGTR2 | c.57C>T (p.His19=) n.525C>T | |
| 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 |