| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128849561A= | CA1742564989 | FLNC | c.5182A= (p.Ser1728=) | |
| 7 | g.128849561A>C | CA369204365 | FLNC | c.5182A>C (p.Ser1728Arg) | |
| 7 | g.128849561A>G | CA369204368 | FLNC | c.5182A>G (p.Ser1728Gly) | ClinVar dbSNP |
| 7 | g.128849561A>T | CA369204369 | FLNC | c.5182A>T (p.Ser1728Cys) | |
| 7 | g.128849562G>A | CA369204371 | FLNC | c.5183G>A (p.Ser1728Asn) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128849562G>C | CA369204374 | FLNC | c.5183G>C (p.Ser1728Thr) | |
| 7 | g.128849562G= | CA1742564994 | FLNC | c.5183G= (p.Ser1728=) | |
| 7 | g.128849562G>T | CA369204373 | FLNC | c.5183G>T (p.Ser1728Ile) | |
| 7 | g.128849563C>A | CA369204376 | FLNC | c.5184C>A (p.Ser1728Arg) | |
| 7 | g.128849563C>G | CA369204377 | FLNC | c.5184C>G (p.Ser1728Arg) | |
| 7 | g.128849563C>T | CA457849120 | FLNC | c.5184C>T (p.Ser1728=) | |
| 7 | g.128849566del | CA2740094844 | FLNC | c.5187del (p.Phe1730SerfsTer?) c.5187del (p.Phe1730SerfsTer20) | ClinVar |
| 7 | g.128849564C>A | CA369204379 | FLNC | c.5185C>A (p.Pro1729Thr) | |
| 7 | g.128849564C>G | CA369204382 | FLNC | c.5185C>G (p.Pro1729Ala) | |
| 7 | g.128849564C>T | CA369204383 | FLNC | c.5185C>T (p.Pro1729Ser) | |
| 7 | g.128849565C>A | CA369204384 | FLNC | c.5186C>A (p.Pro1729His) | ClinVar |
| 7 | g.128849565C>G | CA369204386 | FLNC | c.5186C>G (p.Pro1729Arg) | |
| 7 | g.128849565C>T | CA369204388 | FLNC | c.5186C>T (p.Pro1729Leu) | |
| 7 | g.128849566C>A | CA457849122 | FLNC | c.5187C>A (p.Pro1729=) | |
| 7 | g.128849566C>G | CA457849123 | FLNC | c.5187C>G (p.Pro1729=) | |
| 7 | g.128849566C>T | CA457849124 | FLNC | c.5187C>T (p.Pro1729=) | ClinVar dbSNP |
| 7 | g.128849567T>A | CA369204390 | FLNC | c.5188T>A (p.Phe1730Ile) | |
| 7 | g.128849567T>C | CA369204391 | FLNC | c.5188T>C (p.Phe1730Leu) | |
| 7 | g.128849567T>G | CA369204393 | FLNC | c.5188T>G (p.Phe1730Val) | |
| 7 | g.128849568T>A | CA369204395 | FLNC | c.5189T>A (p.Phe1730Tyr) | |
| 7 | g.128849568T>C | CA369204398 | FLNC | c.5189T>C (p.Phe1730Ser) | |
| 7 | g.128849568T>G | CA369204396 | FLNC | c.5189T>G (p.Phe1730Cys) | |
| 7 | g.128849569C>A | CA369204400 | FLNC | c.5190C>A (p.Phe1730Leu) | |
| 7 | g.128849569C>G | CA369204401 | FLNC | c.5190C>G (p.Phe1730Leu) | |
| 7 | g.128849569C>T | CA457849131 | FLNC | c.5190C>T (p.Phe1730=) | |
| 7 | g.128849570C>A | CA369204403 | FLNC | c.5191C>A (p.His1731Asn) | |
| 7 | g.128849570C= | CA1742565007 | FLNC | c.5191C= (p.His1731=) | |
| 7 | g.128849570C>G | CA369204406 | FLNC | c.5191C>G (p.His1731Asp) | dbSNP gnomAD v4 |
| 7 | g.128849570C>T | CA369204404 | FLNC | c.5191C>T (p.His1731Tyr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128849571A>C | CA369204407 | FLNC | c.5192A>C (p.His1731Pro) | |
| 7 | g.128849571A>G | CA369204408 | FLNC | c.5192A>G (p.His1731Arg) | gnomAD v4 |
| 7 | g.128849571A>T | CA369204409 | FLNC | c.5192A>T (p.His1731Leu) | |
| 7 | g.128849572C>A | CA369204411 | FLNC | c.5193C>A (p.His1731Gln) | |
| 7 | g.128849572C= | CA1742565016 | FLNC | c.5193C= (p.His1731=) | |
| 7 | g.128849572C>G | CA369204412 | FLNC | c.5193C>G (p.His1731Gln) | |
| 7 | g.128849572C>T | CA4475577 | FLNC | c.5193C>T (p.His1731=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128849573G>A | CA4475578 | FLNC | c.5194G>A (p.Val1732Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128849573G>C | CA4475579 | FLNC | c.5194G>C (p.Val1732Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128849573G= | CA1742565024 | FLNC | c.5194G= (p.Val1732=) | |
| 7 | g.128849573G>T | CA369204416 | FLNC | c.5194G>T (p.Val1732Leu) | |
| 7 | g.128849574T>A | CA369204418 | FLNC | c.5195T>A (p.Val1732Glu) | |
| 7 | g.128849574T>C | CA369204419 | FLNC | c.5195T>C (p.Val1732Ala) | |
| 7 | g.128849574T>G | CA369204420 | FLNC | c.5195T>G (p.Val1732Gly) | |
| 7 | g.128849575G>A | CA457849143 | FLNC | c.5196G>A (p.Val1732=) | |
| 7 | g.128849575G>C | CA457849141 | FLNC | c.5196G>C (p.Val1732=) |