Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.148741682C>A | CA354888450 | AGTR1 | c.647C>A (p.Thr216Asn) c.734C>A (p.Thr245Asn) c.752C>A (p.Thr251Asn) | |
3 | g.148741682C= | CA1409910007 | AGTR1 | c.647C= (p.Thr216=) c.734C= (p.Thr245=) c.752C= (p.Thr251=) | |
3 | g.148741682C>G | CA354888452 | AGTR1 | c.647C>G (p.Thr216Ser) c.734C>G (p.Thr245Ser) c.752C>G (p.Thr251Ser) | |
3 | g.148741682C>T | CA85498062 | AGTR1 | c.647C>T (p.Thr216Ile) c.734C>T (p.Thr245Ile) c.752C>T (p.Thr251Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.148741683T>A | CA436389817 | AGTR1 | c.648T>A (p.Thr216=) c.735T>A (p.Thr245=) c.753T>A (p.Thr251=) | |
3 | g.148741683T>C | CA436389818 | AGTR1 | c.648T>C (p.Thr216=) c.735T>C (p.Thr245=) c.753T>C (p.Thr251=) | |
3 | g.148741683T>G | CA436389819 | AGTR1 | c.648T>G (p.Thr216=) c.735T>G (p.Thr245=) c.753T>G (p.Thr251=) | |
3 | g.148741684C>A | CA354888453 | AGTR1 | c.649C>A (p.Leu217Ile) c.736C>A (p.Leu246Ile) c.754C>A (p.Leu252Ile) | |
3 | g.148741684C= | CA1409910011 | AGTR1 | c.649C= (p.Leu217=) c.736C= (p.Leu246=) c.754C= (p.Leu252=) | |
3 | g.148741684C>G | CA354888454 | AGTR1 | c.649C>G (p.Leu217Val) c.736C>G (p.Leu246Val) c.754C>G (p.Leu252Val) | |
3 | g.148741684C>T | CA354888456 | AGTR1 | c.649C>T (p.Leu217Phe) c.736C>T (p.Leu246Phe) c.754C>T (p.Leu252Phe) | dbSNP |
3 | g.148741684_148741688delinsCTTAT | CA1409910009 | AGTR1 | c.649_653delinsCTTAT (p.Leu217=) c.736_740delinsCTTAT (p.Leu246=) c.754_758delinsCTTAT (p.Leu252=) | |
3 | g.148741685T>A | CA354888458 | AGTR1 | c.650T>A (p.Leu217His) c.737T>A (p.Leu246His) c.755T>A (p.Leu252His) | |
3 | g.148741685T>C | CA354888460 | AGTR1 | c.650T>C (p.Leu217Pro) c.737T>C (p.Leu246Pro) c.755T>C (p.Leu252Pro) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.148741685T>G | CA354888461 | AGTR1 | c.650T>G (p.Leu217Arg) c.737T>G (p.Leu246Arg) c.755T>G (p.Leu252Arg) | |
3 | g.148741685T= | CA1409910016 | AGTR1 | c.650T= (p.Leu217=) c.737T= (p.Leu246=) c.755T= (p.Leu252=) | |
3 | g.148741687_148741690del | CA900490604 | AGTR1 | c.652_655del (p.Ile218GlyfsTer4) c.739_742del (p.Ile247GlyfsTer4) c.757_760del (p.Ile253GlyfsTer4) | dbSNP |
3 | g.148741686T>A | CA436389824 | AGTR1 | c.651T>A (p.Leu217=) c.738T>A (p.Leu246=) c.756T>A (p.Leu252=) | |
3 | g.148741686T>C | CA436389825 | AGTR1 | c.651T>C (p.Leu217=) c.738T>C (p.Leu246=) c.756T>C (p.Leu252=) | |
3 | g.148741686T>G | CA436389827 | AGTR1 | c.651T>G (p.Leu217=) c.738T>G (p.Leu246=) c.756T>G (p.Leu252=) | |
3 | g.148741687A>C | CA354888463 | AGTR1 | c.652A>C (p.Ile218Leu) c.739A>C (p.Ile247Leu) c.757A>C (p.Ile253Leu) | |
3 | g.148741687A>G | CA354888465 | AGTR1 | c.652A>G (p.Ile218Val) c.739A>G (p.Ile247Val) c.757A>G (p.Ile253Val) | |
3 | g.148741687A>T | CA354888466 | AGTR1 | c.652A>T (p.Ile218Phe) c.739A>T (p.Ile247Phe) c.757A>T (p.Ile253Phe) | |
3 | g.148741688T>A | CA354888471 | AGTR1 | c.653T>A (p.Ile218Asn) c.740T>A (p.Ile247Asn) c.758T>A (p.Ile253Asn) | |
3 | g.148741688T>C | CA354888470 | AGTR1 | c.653T>C (p.Ile218Thr) c.740T>C (p.Ile247Thr) c.758T>C (p.Ile253Thr) | |
3 | g.148741688T>G | CA2657361 | AGTR1 | c.653T>G (p.Ile218Ser) c.740T>G (p.Ile247Ser) c.758T>G (p.Ile253Ser) | dbSNP ExAC gnomAD v2 |
3 | g.148741688T= | CA1409910019 | AGTR1 | c.653T= (p.Ile218=) c.740T= (p.Ile247=) c.758T= (p.Ile253=) | |
3 | g.148741689T>A | CA436389837 | AGTR1 | c.654T>A (p.Ile218=) c.741T>A (p.Ile247=) c.759T>A (p.Ile253=) | |
3 | g.148741689T>C | CA436389838 | AGTR1 | c.654T>C (p.Ile218=) c.741T>C (p.Ile247=) c.759T>C (p.Ile253=) | |
3 | g.148741689T>G | CA354888474 | AGTR1 | c.654T>G (p.Ile218Met) c.741T>G (p.Ile247Met) c.759T>G (p.Ile253Met) | |
3 | g.148741690T>A | CA354888475 | AGTR1 | c.655T>A (p.Trp219Arg) c.742T>A (p.Trp248Arg) c.760T>A (p.Trp254Arg) | |
3 | g.148741690T>C | CA354888478 | AGTR1 | c.655T>C (p.Trp219Arg) c.742T>C (p.Trp248Arg) c.760T>C (p.Trp254Arg) | COSMIC |
3 | g.148741690T>G | CA354888480 | AGTR1 | c.655T>G (p.Trp219Gly) c.742T>G (p.Trp248Gly) c.760T>G (p.Trp254Gly) | |
3 | g.148741691G>A | CA354888482 | AGTR1 | c.656G>A (p.Trp219Ter) c.743G>A (p.Trp248Ter) c.761G>A (p.Trp254Ter) | COSMIC |
3 | g.148741691G>C | CA354888484 | AGTR1 | c.656G>C (p.Trp219Ser) c.743G>C (p.Trp248Ser) c.761G>C (p.Trp254Ser) | |
3 | g.148741691G>T | CA354888486 | AGTR1 | c.656G>T (p.Trp219Leu) c.743G>T (p.Trp248Leu) c.761G>T (p.Trp254Leu) | |
3 | g.148741692G>A | CA354888488 | AGTR1 | c.657G>A (p.Trp219Ter) c.744G>A (p.Trp248Ter) c.762G>A (p.Trp254Ter) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
3 | g.148741692G>C | CA354888489 | AGTR1 | c.657G>C (p.Trp219Cys) c.744G>C (p.Trp248Cys) c.762G>C (p.Trp254Cys) | |
3 | g.148741692G= | CA1409910022 | AGTR1 | c.657G= (p.Trp219=) c.744G= (p.Trp248=) c.762G= (p.Trp254=) | |
3 | g.148741692G>T | CA354888491 | AGTR1 | c.657G>T (p.Trp219Cys) c.744G>T (p.Trp248Cys) c.762G>T (p.Trp254Cys) | COSMIC |
3 | g.148741693A>C | CA354888492 | AGTR1 | c.658A>C (p.Lys220Gln) c.745A>C (p.Lys249Gln) c.763A>C (p.Lys255Gln) | |
3 | g.148741693A>G | CA354888493 | AGTR1 | c.658A>G (p.Lys220Glu) c.745A>G (p.Lys249Glu) c.763A>G (p.Lys255Glu) | |
3 | g.148741693A>T | CA354888495 | AGTR1 | c.658A>T (p.Lys220Ter) c.745A>T (p.Lys249Ter) c.763A>T (p.Lys255Ter) | |
3 | g.148741694A>C | CA354888499 | AGTR1 | c.659A>C (p.Lys220Thr) c.746A>C (p.Lys249Thr) c.764A>C (p.Lys255Thr) | |
3 | g.148741694A>G | CA354888500 | AGTR1 | c.659A>G (p.Lys220Arg) c.746A>G (p.Lys249Arg) c.764A>G (p.Lys255Arg) | |
3 | g.148741694A>T | CA354888497 | AGTR1 | c.659A>T (p.Lys220Met) c.746A>T (p.Lys249Met) c.764A>T (p.Lys255Met) | |
3 | g.148741695G>A | CA436389853 | AGTR1 | c.660G>A (p.Lys220=) c.747G>A (p.Lys249=) c.765G>A (p.Lys255=) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.148741695G>C | CA354888502 | AGTR1 | c.660G>C (p.Lys220Asn) c.747G>C (p.Lys249Asn) c.765G>C (p.Lys255Asn) | |
3 | g.148741695G= | CA1409910024 | AGTR1 | c.660G= (p.Lys220=) c.747G= (p.Lys249=) c.765G= (p.Lys255=) | |
3 | g.148741695G>T | CA354888505 | AGTR1 | c.660G>T (p.Lys220Asn) c.747G>T (p.Lys249Asn) c.765G>T (p.Lys255Asn) | dbSNP gnomAD v4 |