| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128837493T>A | CA457846391 | FLNC | c.795T>A (p.Gly265=) | |
| 7 | g.128837493T>C | CA152884 | FLNC | c.795T>C (p.Gly265=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128837493T>G | CA457846393 | FLNC | c.795T>G (p.Gly265=) | |
| 7 | g.128837493T= | CA1742520959 | FLNC | c.795T= (p.Gly265=) | |
| 7 | g.128837494G>A | CA369222484 | FLNC | c.796G>A (p.Ala266Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128837494G>C | CA369222486 | FLNC | c.796G>C (p.Ala266Pro) | |
| 7 | g.128837494G= | CA1742544683 | FLNC | c.796G= (p.Ala266=) | |
| 7 | g.128837494G>T | CA369222489 | FLNC | c.796G>T (p.Ala266Ser) | |
| 7 | g.128837495C>A | CA369222496 | FLNC | c.797C>A (p.Ala266Asp) | gnomAD v4 |
| 7 | g.128837495C>G | CA369222498 | FLNC | c.797C>G (p.Ala266Gly) | |
| 7 | g.128837495C>T | CA369222500 | FLNC | c.797C>T (p.Ala266Val) | ClinVar |
| 7 | g.128837496C>A | CA457846398 | FLNC | c.798C>A (p.Ala266=) | gnomAD v4 |
| 7 | g.128837496C= | CA1742544684 | FLNC | c.798C= (p.Ala266=) | |
| 7 | g.128837496C>G | CA457846399 | FLNC | c.798C>G (p.Ala266=) | |
| 7 | g.128837496C>T | CA457846400 | FLNC | c.798C>T (p.Ala266=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128837497C>A | CA369222503 | FLNC | c.799C>A (p.Pro267Thr) | |
| 7 | g.128837497C>G | CA369222506 | FLNC | c.799C>G (p.Pro267Ala) | |
| 7 | g.128837497C>T | CA369222508 | FLNC | c.799C>T (p.Pro267Ser) | |
| 7 | g.128837497_128837499delinsCCT | CA1742544685 | FLNC | c.799_801delinsCCT (p.Pro267=) | |
| 7 | g.128837498C>A | CA369222511 | FLNC | c.800C>A (p.Pro267His) | |
| 7 | g.128837498C>G | CA369222513 | FLNC | c.800C>G (p.Pro267Arg) | |
| 7 | g.128837498C>T | CA369222515 | FLNC | c.800C>T (p.Pro267Leu) | |
| 7 | g.128837498_128837499del | CA833133564 | FLNC | c.800_801del (p.Pro267ArgfsTer?) | dbSNP gnomAD v4 |
| 7 | g.128837499del | CA2573052811 | FLNC | c.801del (p.Val268PhefsTer6) | ClinVar dbSNP |
| 7 | g.128837499T>A | CA457846407 | FLNC | c.801T>A (p.Pro267=) | |
| 7 | g.128837499T>C | CA457846406 | FLNC | c.801T>C (p.Pro267=) | |
| 7 | g.128837499T>G | CA457846405 | FLNC | c.801T>G (p.Pro267=) | |
| 7 | g.128837500G>A | CA369222523 | FLNC | c.802G>A (p.Val268Ile) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128837500G>C | CA369222517 | FLNC | c.802G>C (p.Val268Leu) | |
| 7 | g.128837500G= | CA1742544686 | FLNC | c.802G= (p.Val268=) | |
| 7 | g.128837500G>T | CA369222520 | FLNC | c.802G>T (p.Val268Phe) | |
| 7 | g.128837501T>A | CA369222525 | FLNC | c.803T>A (p.Val268Asp) | |
| 7 | g.128837501T>C | CA369222526 | FLNC | c.803T>C (p.Val268Ala) | |
| 7 | g.128837501T>G | CA369222527 | FLNC | c.803T>G (p.Val268Gly) | |
| 7 | g.128837502del | CA2740097534 | FLNC | c.804del (p.Arg269AspfsTer5) | ClinVar |
| 7 | g.128837502T>A | CA457846411 | FLNC | c.804T>A (p.Val268=) | |
| 7 | g.128837502T>C | CA4474125 | FLNC | c.804T>C (p.Val268=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128837502T>G | CA457846413 | FLNC | c.804T>G (p.Val268=) | |
| 7 | g.128837502T= | CA1742544687 | FLNC | c.804T= (p.Val268=) | |
| 7 | g.128837503C>A | CA457846414 | FLNC | c.805C>A (p.Arg269=) | gnomAD v4 |
| 7 | g.128837503C= | CA1742544688 | FLNC | c.805C= (p.Arg269=) | |
| 7 | g.128837503C>G | CA369222528 | FLNC | c.805C>G (p.Arg269Gly) | |
| 7 | g.128837503C>T | CA4474126 | FLNC | c.805C>T (p.Arg269Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.128837504G>A | CA369222539 | FLNC | c.806G>A (p.Arg269Gln) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128837504G>C | CA369222541 | FLNC | c.806G>C (p.Arg269Pro) | gnomAD v4 |
| 7 | g.128837504G= | CA1742544689 | FLNC | c.806G= (p.Arg269=) | |
| 7 | g.128837504G>T | CA369222544 | FLNC | c.806G>T (p.Arg269Leu) | |
| 7 | g.128837505A= | CA1742544690 | FLNC | c.807A= (p.Arg269=) | |
| 7 | g.128837505A>C | CA457846418 | FLNC | c.807A>C (p.Arg269=) | |
| 7 | g.128837505A>G | CA457846419 | FLNC | c.807A>G (p.Arg269=) | gnomAD v4 |