Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.148741795A>C | CA354888991 | AGTR1 | c.760A>C (p.Ile254Leu) c.847A>C (p.Ile283Leu) c.865A>C (p.Ile289Leu) | |
3 | g.148741795A>G | CA354888995 | AGTR1 | c.760A>G (p.Ile254Val) c.847A>G (p.Ile283Val) c.865A>G (p.Ile289Val) | |
3 | g.148741795A>T | CA354888989 | AGTR1 | c.760A>T (p.Ile254Phe) c.847A>T (p.Ile283Phe) c.865A>T (p.Ile289Phe) | |
3 | g.148741796T>A | CA354889000 | AGTR1 | c.761T>A (p.Ile254Asn) c.848T>A (p.Ile283Asn) c.866T>A (p.Ile289Asn) | ClinVar dbSNP |
3 | g.148741796T>C | CA354888998 | AGTR1 | c.761T>C (p.Ile254Thr) c.848T>C (p.Ile283Thr) c.866T>C (p.Ile289Thr) | |
3 | g.148741796T>G | CA354889001 | AGTR1 | c.761T>G (p.Ile254Ser) c.848T>G (p.Ile283Ser) c.866T>G (p.Ile289Ser) | |
3 | g.148741797T>A | CA436389594 | AGTR1 | c.762T>A (p.Ile254=) c.849T>A (p.Ile283=) c.867T>A (p.Ile289=) | |
3 | g.148741797T>C | CA436389595 | AGTR1 | c.762T>C (p.Ile254=) c.849T>C (p.Ile283=) c.867T>C (p.Ile289=) | |
3 | g.148741797T>G | CA354889003 | AGTR1 | c.762T>G (p.Ile254Met) c.849T>G (p.Ile283Met) c.867T>G (p.Ile289Met) | |
3 | g.148741798C>A | CA354889014 | AGTR1 | c.763C>A (p.Pro255Thr) c.850C>A (p.Pro284Thr) c.868C>A (p.Pro290Thr) | gnomAD v4 |
3 | g.148741798C>G | CA354889006 | AGTR1 | c.763C>G (p.Pro255Ala) c.850C>G (p.Pro284Ala) c.868C>G (p.Pro290Ala) | |
3 | g.148741798C>T | CA354889008 | AGTR1 | c.763C>T (p.Pro255Ser) c.850C>T (p.Pro284Ser) c.868C>T (p.Pro290Ser) | gnomAD v4 |
3 | g.148741799C>A | CA354889016 | AGTR1 | c.764C>A (p.Pro255His) c.851C>A (p.Pro284His) c.869C>A (p.Pro290His) | |
3 | g.148741799C= | CA1409910170 | AGTR1 | c.764C= (p.Pro255=) c.851C= (p.Pro284=) c.869C= (p.Pro290=) | |
3 | g.148741799C>G | CA354889018 | AGTR1 | c.764C>G (p.Pro255Arg) c.851C>G (p.Pro284Arg) c.869C>G (p.Pro290Arg) | |
3 | g.148741799C>T | CA10617600 | AGTR1 | c.764C>T (p.Pro255Leu) c.851C>T (p.Pro284Leu) c.869C>T (p.Pro290Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
3 | g.148741800C>A | CA2657383 | AGTR1 | c.765C>A (p.Pro255=) c.852C>A (p.Pro284=) c.870C>A (p.Pro290=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.148741800C= | CA1409910176 | AGTR1 | c.765C= (p.Pro255=) c.852C= (p.Pro284=) c.870C= (p.Pro290=) | |
3 | g.148741800C>G | CA436389598 | AGTR1 | c.765C>G (p.Pro255=) c.852C>G (p.Pro284=) c.870C>G (p.Pro290=) | |
3 | g.148741800C>T | CA436389600 | AGTR1 | c.765C>T (p.Pro255=) c.852C>T (p.Pro284=) c.870C>T (p.Pro290=) | |
3 | g.148741801C>A | CA2657384 | AGTR1 | c.766C>A (p.His256Asn) c.853C>A (p.His285Asn) c.871C>A (p.His291Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
3 | g.148741801C= | CA1409910178 | AGTR1 | c.766C= (p.His256=) c.853C= (p.His285=) c.871C= (p.His291=) | |
3 | g.148741801C>G | CA354889024 | AGTR1 | c.766C>G (p.His256Asp) c.853C>G (p.His285Asp) c.871C>G (p.His291Asp) | |
3 | g.148741801C>T | CA354889025 | AGTR1 | c.766C>T (p.His256Tyr) c.853C>T (p.His285Tyr) c.871C>T (p.His291Tyr) | |
3 | g.148741802A>C | CA354889026 | AGTR1 | c.767A>C (p.His256Pro) c.854A>C (p.His285Pro) c.872A>C (p.His291Pro) | |
3 | g.148741802A>G | CA354889027 | AGTR1 | c.767A>G (p.His256Arg) c.854A>G (p.His285Arg) c.872A>G (p.His291Arg) | |
3 | g.148741802A>T | CA354889029 | AGTR1 | c.767A>T (p.His256Leu) c.854A>T (p.His285Leu) c.872A>T (p.His291Leu) | |
3 | g.148741803C>A | CA354889031 | AGTR1 | c.768C>A (p.His256Gln) c.855C>A (p.His285Gln) c.873C>A (p.His291Gln) | gnomAD v4 |
3 | g.148741803C= | CA1409910179 | AGTR1 | c.768C= (p.His256=) c.855C= (p.His285=) c.873C= (p.His291=) | |
3 | g.148741803C>G | CA354889032 | AGTR1 | c.768C>G (p.His256Gln) c.855C>G (p.His285Gln) c.873C>G (p.His291Gln) | gnomAD v4 |
3 | g.148741803C>T | CA436389601 | AGTR1 | c.768C>T (p.His256=) c.855C>T (p.His285=) c.873C>T (p.His291=) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.148741804C>A | CA354889034 | AGTR1 | c.769C>A (p.Gln257Lys) c.856C>A (p.Gln286Lys) c.874C>A (p.Gln292Lys) | gnomAD v4 |
3 | g.148741804C= | CA1409910182 | AGTR1 | c.769C= (p.Gln257=) c.856C= (p.Gln286=) c.874C= (p.Gln292=) | |
3 | g.148741804C>G | CA354889035 | AGTR1 | c.769C>G (p.Gln257Glu) c.856C>G (p.Gln286Glu) c.874C>G (p.Gln292Glu) | gnomAD v4 |
3 | g.148741804C>T | CA2657385 | AGTR1 | c.769C>T (p.Gln257Ter) c.856C>T (p.Gln286Ter) c.874C>T (p.Gln292Ter) | dbSNP ExAC gnomAD v2 |
3 | g.148741805A>C | CA354889036 | AGTR1 | c.770A>C (p.Gln257Pro) c.857A>C (p.Gln286Pro) c.875A>C (p.Gln292Pro) | |
3 | g.148741805A>G | CA354889038 | AGTR1 | c.770A>G (p.Gln257Arg) c.857A>G (p.Gln286Arg) c.875A>G (p.Gln292Arg) | |
3 | g.148741805A>T | CA354889040 | AGTR1 | c.770A>T (p.Gln257Leu) c.857A>T (p.Gln286Leu) c.875A>T (p.Gln292Leu) | |
3 | g.148741806A>C | CA354889041 | AGTR1 | c.771A>C (p.Gln257His) c.858A>C (p.Gln286His) c.876A>C (p.Gln292His) | |
3 | g.148741806A>G | CA436389603 | AGTR1 | c.771A>G (p.Gln257=) c.858A>G (p.Gln286=) c.876A>G (p.Gln292=) | |
3 | g.148741806A>T | CA354889043 | AGTR1 | c.771A>T (p.Gln257His) c.858A>T (p.Gln286His) c.876A>T (p.Gln292His) | |
3 | g.148741807A>C | CA354889044 | AGTR1 | c.772A>C (p.Ile258Leu) c.859A>C (p.Ile287Leu) c.877A>C (p.Ile293Leu) | |
3 | g.148741807A>G | CA354889046 | AGTR1 | c.772A>G (p.Ile258Val) c.859A>G (p.Ile287Val) c.877A>G (p.Ile293Val) | |
3 | g.148741807A>T | CA354889047 | AGTR1 | c.772A>T (p.Ile258Leu) c.859A>T (p.Ile287Leu) c.877A>T (p.Ile293Leu) | |
3 | g.148741809_148741810del | CA2668116565 | AGTR1 | c.774_775del (p.Phe259HisfsTer14) c.861_862del (p.Phe288HisfsTer14) c.879_880del (p.Phe294HisfsTer14) | gnomAD v4 |
3 | g.148741808T>A | CA354889056 | AGTR1 | c.773T>A (p.Ile258Lys) c.860T>A (p.Ile287Lys) c.878T>A (p.Ile293Lys) | |
3 | g.148741808T>C | CA2657386 | AGTR1 | c.773T>C (p.Ile258Thr) c.860T>C (p.Ile287Thr) c.878T>C (p.Ile293Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.148741808T>G | CA354889051 | AGTR1 | c.773T>G (p.Ile258Arg) c.860T>G (p.Ile287Arg) c.878T>G (p.Ile293Arg) | |
3 | g.148741808T= | CA1409910184 | AGTR1 | c.773T= (p.Ile258=) c.860T= (p.Ile287=) c.878T= (p.Ile293=) | |
3 | g.148741809A= | CA1409910187 | AGTR1 | c.774A= (p.Ile258=) c.861A= (p.Ile287=) c.879A= (p.Ile293=) |