Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.116172237dup | CA2453331637 | AGTR2 | c.-35-9dup (n.-35-9dup) n.425dup | dbSNP |
X | g.116172237del | CA2579684208 | AGTR2 | c.-35-9del (n.-35-9del) n.425del | gnomAD v4 |
X | g.116172236T>C | CA2694510848 | AGTR2 | c.-35-10T>C (n.-35-10T>C) n.424T>C | gnomAD v4 |
X | g.116172237T>C | CA2741787848 | AGTR2 | c.-35-9T>C (n.-35-9T>C) n.425T>C | |
X | g.116172238C= | CA2453331641 | AGTR2 | c.-35-8C= (n.-35-8C=) n.426C= | |
X | g.116172238C>G | CA1136568811 | AGTR2 | c.-35-8C>G (n.-35-8C>G) n.426C>G | dbSNP gnomAD v3 gnomAD v4 |
X | g.116172241C= | CA2453331642 | AGTR2 | c.-35-5C= (n.-35-5C=) n.429C= | |
X | g.116172241C>T | CA334723675 | AGTR2 | c.-35-5C>T (n.-35-5C>T) n.429C>T | dbSNP gnomAD v4 |
X | g.116172242A>C | CA658450243 | AGTR2 | c.-35-4A>C (n.-35-4A>C) n.430A>C | COSMIC |
X | g.116172242A>G | CA2694510849 | AGTR2 | c.-35-4A>G (n.-35-4A>G) n.430A>G | gnomAD v4 |
X | g.116172243C>A | CA2694510850 | AGTR2 | c.-35-3C>A (n.-35-3C>A) n.431C>A | gnomAD v4 |
X | g.116172243C>T | CA2694510851 | AGTR2 | c.-35-3C>T (n.-35-3C>T) n.431C>T | gnomAD v4 |
X | g.116172244A>C | CA658450244 | AGTR2 | c.-35-2A>C (n.-35-2A>C) n.432A>C | COSMIC |
X | g.116172247dup | CA658450247 | AGTR2 | c.-34dup (n.-34dup) n.435dup | COSMIC COSMIC |
X | g.116172249G>T | CA2694510852 | AGTR2 | c.-32G>T (n.-32G>T) n.437G>T | gnomAD v4 |
X | g.116172251A= | CA2453331643 | AGTR2 | c.-30A= (n.-30A=) n.439A= | |
X | g.116172251A>C | CA2694510853 | AGTR2 | c.-30A>C (n.-30A>C) n.439A>C | gnomAD v4 |
X | g.116172251A>G | CA10497220 | AGTR2 | c.-30A>G (n.-30A>G) n.439A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.116172255G>A | CA2579684209 | AGTR2 | c.-26G>A (n.-26G>A) n.443G>A | |
X | g.116172259T>A | CA10497221 | AGTR2 | c.-22T>A (n.-22T>A) n.447T>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.116172259T= | CA2453331645 | AGTR2 | c.-22T= (n.-22T=) n.447T= | |
X | g.116172259_116172260delinsTA | CA2453331644 | AGTR2 | c.-22_-21delinsTA (n.-22_-21delinsTA) n.447_448delinsTA | |
X | g.116172260del | CA2453331646 | AGTR2 | c.-21del (n.-21del) n.448del | dbSNP gnomAD v4 |
X | g.116172261G>A | CA2694510854 | AGTR2 | c.-20G>A (n.-20G>A) n.449G>A | gnomAD v4 |
X | g.116172261G>C | CA2453331648 | AGTR2 | c.-20G>C (n.-20G>C) n.449G>C | dbSNP |
X | g.116172261G= | CA2453331647 | AGTR2 | c.-20G= (n.-20G=) n.449G= | |
X | g.116172262G>A | CA2579684210 | AGTR2 | c.-19G>A (n.-19G>A) n.450G>A | |
X | g.116172262G= | CA2453331649 | AGTR2 | c.-19G= (n.-19G=) n.450G= | |
X | g.116172262G>T | CA2453331650 | AGTR2 | c.-19G>T (n.-19G>T) n.450G>T | dbSNP gnomAD v4 |
X | g.116172265C>A | CA2694510855 | AGTR2 | c.-16C>A (n.-16C>A) n.453C>A | gnomAD v4 |
X | g.116172270G>C | CA2453331652 | AGTR2 | c.-11G>C (n.-11G>C) n.458G>C | dbSNP |
X | g.116172270G= | CA2453331651 | AGTR2 | c.-11G= (n.-11G=) n.458G= | |
X | g.116172273A>C | CA2823125651 | AGTR2 | c.-8A>C (n.-8A>C) n.461A>C | |
X | g.116172273A>T | CA2694510856 | AGTR2 | c.-8A>T (n.-8A>T) n.461A>T | gnomAD v4 |
X | g.116172277C= | CA2453331653 | AGTR2 | c.-4C= (n.-4C=) n.465C= | |
X | g.116172277C>T | CA644065570 | AGTR2 | c.-4C>T (n.-4C>T) n.465C>T | dbSNP gnomAD v2 gnomAD v4 |
X | g.116172278A>G | CA2694510857 | AGTR2 | c.-3A>G (n.-3A>G) n.466A>G | gnomAD v4 |
X | g.116172279A= | CA2453331654 | AGTR2 | c.-2A= (n.-2A=) n.467A= | |
X | g.116172279A>G | CA644065571 | AGTR2 | c.-2A>G (n.-2A>G) n.467A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.116172281A>C | CA414337367 | AGTR2 | c.1A>C (p.Met1Leu) n.469A>C | |
X | g.116172281A>G | CA414337368 | AGTR2 | c.1A>G (p.Met1Val) n.469A>G | |
X | g.116172281A>T | CA414337369 | AGTR2 | c.1A>T (p.Met1Leu) n.469A>T | |
X | g.116172282T>A | CA414337372 | AGTR2 | c.2T>A (p.Met1Lys) n.470T>A | |
X | g.116172282T>C | CA414337371 | AGTR2 | c.2T>C (p.Met1Thr) n.470T>C | gnomAD v4 |
X | g.116172282T>G | CA414337370 | AGTR2 | c.2T>G (p.Met1Arg) n.470T>G | |
X | g.116172283G>A | CA414337373 | AGTR2 | c.3G>A (p.Met1Ile) n.471G>A | |
X | g.116172283G>C | CA414337374 | AGTR2 | c.3G>C (p.Met1Ile) n.471G>C | |
X | g.116172283G= | CA2453331655 | AGTR2 | c.3G= (p.Met1=) n.471G= | |
X | g.116172283G>T | CA414337375 | AGTR2 | c.3G>T (p.Met1Ile) n.471G>T | dbSNP gnomAD v3 gnomAD v4 |
X | g.116172284A>C | CA414337376 | AGTR2 | c.4A>C (p.Lys2Gln) n.472A>C | |
X | g.116172284A>G | CA414337377 | AGTR2 | c.4A>G (p.Lys2Glu) n.472A>G | |
X | g.116172284A>T | CA414337378 | AGTR2 | c.4A>T (p.Lys2Ter) n.472A>T | |
X | g.116172285A= | CA2453331656 | AGTR2 | c.5A= (p.Lys2=) n.473A= | |
X | g.116172285A>C | CA414337379 | AGTR2 | c.5A>C (p.Lys2Thr) n.473A>C | |
X | g.116172285A>G | CA414337381 | AGTR2 | c.5A>G (p.Lys2Arg) n.473A>G | dbSNP gnomAD v2 |
X | g.116172285A>T | CA414337380 | AGTR2 | c.5A>T (p.Lys2Met) n.473A>T | |
X | g.116172286G>A | CA518449092 | AGTR2 | c.6G>A (p.Lys2=) n.474G>A | gnomAD v4 |
X | g.116172286G>C | CA414337382 | AGTR2 | c.6G>C (p.Lys2Asn) n.474G>C | |
X | g.116172286G>T | CA414337383 | AGTR2 | c.6G>T (p.Lys2Asn) n.474G>T | |
X | g.116172287G>A | CA414337384 | AGTR2 | c.7G>A (p.Gly3Ser) n.475G>A | |
X | g.116172287G>C | CA414337385 | AGTR2 | c.7G>C (p.Gly3Arg) n.475G>C | |
X | g.116172287G>T | CA414337386 | AGTR2 | c.7G>T (p.Gly3Cys) n.475G>T | |
X | g.116172288G>A | CA414337387 | AGTR2 | c.8G>A (p.Gly3Asp) n.476G>A | gnomAD v4 |
X | g.116172288G>C | CA414337388 | AGTR2 | c.8G>C (p.Gly3Ala) n.476G>C | |
X | g.116172288G>T | CA414337389 | AGTR2 | c.8G>T (p.Gly3Val) n.476G>T | |
X | g.116172289C>A | CA518449095 | AGTR2 | c.9C>A (p.Gly3=) n.477C>A | |
X | g.116172289C>G | CA518449094 | AGTR2 | c.9C>G (p.Gly3=) n.477C>G | |
X | g.116172289C>T | CA518449093 | AGTR2 | c.9C>T (p.Gly3=) n.477C>T | |
X | g.116172290A>C | CA414337390 | AGTR2 | c.10A>C (p.Asn4His) n.478A>C | |
X | g.116172290A>G | CA414337391 | AGTR2 | c.10A>G (p.Asn4Asp) n.478A>G | |
X | g.116172290A>T | CA414337392 | AGTR2 | c.10A>T (p.Asn4Tyr) n.478A>T | |
X | g.116172291A>C | CA414337395 | AGTR2 | c.11A>C (p.Asn4Thr) n.479A>C | |
X | g.116172291A>G | CA414337394 | AGTR2 | c.11A>G (p.Asn4Ser) n.479A>G | gnomAD v4 |
X | g.116172291A>T | CA414337393 | AGTR2 | c.11A>T (p.Asn4Ile) n.479A>T | |
X | g.116172292C>A | CA414337396 | AGTR2 | c.12C>A (p.Asn4Lys) n.480C>A | |
X | g.116172292C>G | CA414337397 | AGTR2 | c.12C>G (p.Asn4Lys) n.480C>G | gnomAD v4 |
X | g.116172292C>T | CA518449096 | AGTR2 | c.12C>T (p.Asn4=) n.480C>T | |
X | g.116172293T>A | CA414337398 | AGTR2 | c.13T>A (p.Ser5Thr) n.481T>A | |
X | g.116172293T>C | CA414337399 | AGTR2 | c.13T>C (p.Ser5Pro) n.481T>C | |
X | g.116172293T>G | CA414337400 | AGTR2 | c.13T>G (p.Ser5Ala) n.481T>G | |
X | g.116172294C>A | CA414337401 | AGTR2 | c.14C>A (p.Ser5Tyr) n.482C>A | |
X | g.116172294C>G | CA414337402 | AGTR2 | c.14C>G (p.Ser5Cys) n.482C>G | |
X | g.116172294C>T | CA414337403 | AGTR2 | c.14C>T (p.Ser5Phe) n.482C>T | |
X | g.116172295C>A | CA518449097 | AGTR2 | c.15C>A (p.Ser5=) n.483C>A | |
X | g.116172295C>G | CA518449098 | AGTR2 | c.15C>G (p.Ser5=) n.483C>G | |
X | g.116172295C>T | CA518449099 | AGTR2 | c.15C>T (p.Ser5=) n.483C>T | gnomAD v4 |
X | g.116172296del | CA2694510858 | AGTR2 | c.16del (p.Thr6ProfsTer18) n.484del | gnomAD v4 |
X | g.116172296A>C | CA414337404 | AGTR2 | c.16A>C (p.Thr6Pro) n.484A>C | |
X | g.116172296A>G | CA414337405 | AGTR2 | c.16A>G (p.Thr6Ala) n.484A>G | |
X | g.116172296A>T | CA414337406 | AGTR2 | c.16A>T (p.Thr6Ser) n.484A>T | |
X | g.116172297C>A | CA414337407 | AGTR2 | c.17C>A (p.Thr6Asn) n.485C>A | |
X | g.116172297C>G | CA414337408 | AGTR2 | c.17C>G (p.Thr6Ser) n.485C>G | |
X | g.116172297C>T | CA414337409 | AGTR2 | c.17C>T (p.Thr6Ile) n.485C>T | |
X | g.116172298C>A | CA518449100 | AGTR2 | c.18C>A (p.Thr6=) n.486C>A | dbSNP gnomAD v3 gnomAD v4 |
X | g.116172298C= | CA2453331657 | AGTR2 | c.18C= (p.Thr6=) n.486C= | |
X | g.116172298C>G | CA518449101 | AGTR2 | c.18C>G (p.Thr6=) n.486C>G | |
X | g.116172298C>T | CA10497222 | AGTR2 | c.18C>T (p.Thr6=) n.486C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
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 |