| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.148741880C>A | CA354889350 | AGTR1 | c.845C>A (p.Thr282Lys) c.932C>A (p.Thr311Lys) c.950C>A (p.Thr317Lys) | |
| 3 | g.148741880C= | CA1409910253 | AGTR1 | c.845C= (p.Thr282=) c.932C= (p.Thr311=) c.950C= (p.Thr317=) | |
| 3 | g.148741880C>G | CA354889351 | AGTR1 | c.845C>G (p.Thr282Arg) c.932C>G (p.Thr311Arg) c.950C>G (p.Thr317Arg) | |
| 3 | g.148741880C>T | CA127782 | AGTR1 | c.845C>T (p.Thr282Met) c.932C>T (p.Thr311Met) c.950C>T (p.Thr317Met) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.148741881G>A | CA2657396 | AGTR1 | c.846G>A (p.Thr282=) c.933G>A (p.Thr311=) c.951G>A (p.Thr317=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.148741881G>C | CA436389685 | AGTR1 | c.846G>C (p.Thr282=) c.933G>C (p.Thr311=) c.951G>C (p.Thr317=) | |
| 3 | g.148741881G= | CA1409910259 | AGTR1 | c.846G= (p.Thr282=) c.933G= (p.Thr311=) c.951G= (p.Thr317=) | |
| 3 | g.148741881G>T | CA436389686 | AGTR1 | c.846G>T (p.Thr282=) c.933G>T (p.Thr311=) c.951G>T (p.Thr317=) | dbSNP |
| 3 | g.148741882G>A | CA2657397 | AGTR1 | c.847G>A (p.Ala283Thr) c.934G>A (p.Ala312Thr) c.952G>A (p.Ala318Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 3 | g.148741882G>C | CA354889352 | AGTR1 | c.847G>C (p.Ala283Pro) c.934G>C (p.Ala312Pro) c.952G>C (p.Ala318Pro) | |
| 3 | g.148741882G= | CA1409910263 | AGTR1 | c.847G= (p.Ala283=) c.934G= (p.Ala312=) c.952G= (p.Ala318=) | |
| 3 | g.148741882G>T | CA354889353 | AGTR1 | c.847G>T (p.Ala283Ser) c.934G>T (p.Ala312Ser) c.952G>T (p.Ala318Ser) | |
| 3 | g.148741883C>A | CA354889354 | AGTR1 | c.848C>A (p.Ala283Asp) c.935C>A (p.Ala312Asp) c.953C>A (p.Ala318Asp) | |
| 3 | g.148741883C>G | CA354889356 | AGTR1 | c.848C>G (p.Ala283Gly) c.935C>G (p.Ala312Gly) c.953C>G (p.Ala318Gly) | |
| 3 | g.148741883C>T | CA354889355 | AGTR1 | c.848C>T (p.Ala283Val) c.935C>T (p.Ala312Val) c.953C>T (p.Ala318Val) | |
| 3 | g.148741884C>A | CA436389688 | AGTR1 | c.849C>A (p.Ala283=) c.936C>A (p.Ala312=) c.954C>A (p.Ala318=) | |
| 3 | g.148741884C>G | CA436389691 | AGTR1 | c.849C>G (p.Ala283=) c.936C>G (p.Ala312=) c.954C>G (p.Ala318=) | |
| 3 | g.148741884C>T | CA436389689 | AGTR1 | c.849C>T (p.Ala283=) c.936C>T (p.Ala312=) c.954C>T (p.Ala318=) | |
| 3 | g.148741885A>C | CA354889357 | AGTR1 | c.850A>C (p.Met284Leu) c.937A>C (p.Met313Leu) c.955A>C (p.Met319Leu) | |
| 3 | g.148741885A>G | CA354889358 | AGTR1 | c.850A>G (p.Met284Val) c.937A>G (p.Met313Val) c.955A>G (p.Met319Val) | COSMIC |
| 3 | g.148741885A>T | CA354889359 | AGTR1 | c.850A>T (p.Met284Leu) c.937A>T (p.Met313Leu) c.955A>T (p.Met319Leu) | |
| 3 | g.148741886T>A | CA354889360 | AGTR1 | c.851T>A (p.Met284Lys) c.938T>A (p.Met313Lys) c.956T>A (p.Met319Lys) | |
| 3 | g.148741886T>C | CA354889361 | AGTR1 | c.851T>C (p.Met284Thr) c.938T>C (p.Met313Thr) c.956T>C (p.Met319Thr) | |
| 3 | g.148741886T>G | CA354889362 | AGTR1 | c.851T>G (p.Met284Arg) c.938T>G (p.Met313Arg) c.956T>G (p.Met319Arg) | |
| 3 | g.148741887G>A | CA354889363 | AGTR1 | c.852G>A (p.Met284Ile) c.939G>A (p.Met313Ile) c.957G>A (p.Met319Ile) | |
| 3 | g.148741887G>C | CA354889364 | AGTR1 | c.852G>C (p.Met284Ile) c.939G>C (p.Met313Ile) c.957G>C (p.Met319Ile) | |
| 3 | g.148741887G>T | CA354889365 | AGTR1 | c.852G>T (p.Met284Ile) c.939G>T (p.Met313Ile) c.957G>T (p.Met319Ile) | |
| 3 | g.148741888C>A | CA354889366 | AGTR1 | c.853C>A (p.Pro285Thr) c.940C>A (p.Pro314Thr) c.958C>A (p.Pro320Thr) | |
| 3 | g.148741888C>G | CA354889367 | AGTR1 | c.853C>G (p.Pro285Ala) c.940C>G (p.Pro314Ala) c.958C>G (p.Pro320Ala) | |
| 3 | g.148741888C>T | CA354889368 | AGTR1 | c.853C>T (p.Pro285Ser) c.940C>T (p.Pro314Ser) c.958C>T (p.Pro320Ser) | |
| 3 | g.148741889C>A | CA354889369 | AGTR1 | c.854C>A (p.Pro285His) c.941C>A (p.Pro314His) c.959C>A (p.Pro320His) | |
| 3 | g.148741889C>G | CA354889371 | AGTR1 | c.854C>G (p.Pro285Arg) c.941C>G (p.Pro314Arg) c.959C>G (p.Pro320Arg) | gnomAD v4 |
| 3 | g.148741889C>T | CA354889370 | AGTR1 | c.854C>T (p.Pro285Leu) c.941C>T (p.Pro314Leu) c.959C>T (p.Pro320Leu) | |
| 3 | g.148741890T>A | CA2657398 | AGTR1 | c.855T>A (p.Pro285=) c.942T>A (p.Pro314=) c.960T>A (p.Pro320=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.148741890T>C | CA85498531 | AGTR1 | c.855T>C (p.Pro285=) c.942T>C (p.Pro314=) c.960T>C (p.Pro320=) | dbSNP gnomAD v4 |
| 3 | g.148741890T>G | CA436389700 | AGTR1 | c.855T>G (p.Pro285=) c.942T>G (p.Pro314=) c.960T>G (p.Pro320=) | |
| 3 | g.148741890T= | CA1409910266 | AGTR1 | c.855T= (p.Pro285=) c.942T= (p.Pro314=) c.960T= (p.Pro320=) | |
| 3 | g.148741891A= | CA1409910269 | AGTR1 | c.856A= (p.Ile286=) c.943A= (p.Ile315=) c.961A= (p.Ile321=) | |
| 3 | g.148741891A>C | CA354889372 | AGTR1 | c.856A>C (p.Ile286Leu) c.943A>C (p.Ile315Leu) c.961A>C (p.Ile321Leu) | |
| 3 | g.148741891A>G | CA354889373 | AGTR1 | c.856A>G (p.Ile286Val) c.943A>G (p.Ile315Val) c.961A>G (p.Ile321Val) | dbSNP gnomAD v4 |
| 3 | g.148741891A>T | CA354889374 | AGTR1 | c.856A>T (p.Ile286Phe) c.943A>T (p.Ile315Phe) c.961A>T (p.Ile321Phe) | |
| 3 | g.148741891_148741894dup | CA2668116566 | AGTR1 | c.856_859dup (p.Thr287AsnfsTer9) c.943_946dup (p.Thr316AsnfsTer9) c.961_964dup (p.Thr322AsnfsTer9) | gnomAD v4 |
| 3 | g.148741892T>A | CA354889375 | AGTR1 | c.857T>A (p.Ile286Asn) c.944T>A (p.Ile315Asn) c.962T>A (p.Ile321Asn) | |
| 3 | g.148741892T>C | CA354889376 | AGTR1 | c.857T>C (p.Ile286Thr) c.944T>C (p.Ile315Thr) c.962T>C (p.Ile321Thr) | |
| 3 | g.148741892T>G | CA354889377 | AGTR1 | c.857T>G (p.Ile286Ser) c.944T>G (p.Ile315Ser) c.962T>G (p.Ile321Ser) | |
| 3 | g.148741893C>A | CA436389821 | AGTR1 | c.858C>A (p.Ile286=) c.945C>A (p.Ile315=) c.963C>A (p.Ile321=) | |
| 3 | g.148741893C>G | CA354889378 | AGTR1 | c.858C>G (p.Ile286Met) c.945C>G (p.Ile315Met) c.963C>G (p.Ile321Met) | |
| 3 | g.148741893C>T | CA436389823 | AGTR1 | c.858C>T (p.Ile286=) c.945C>T (p.Ile315=) c.963C>T (p.Ile321=) | |
| 3 | g.148741894A>C | CA354889379 | AGTR1 | c.859A>C (p.Thr287Pro) c.946A>C (p.Thr316Pro) c.964A>C (p.Thr322Pro) | |
| 3 | g.148741894A>G | CA354889380 | AGTR1 | c.859A>G (p.Thr287Ala) c.946A>G (p.Thr316Ala) c.964A>G (p.Thr322Ala) |