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