| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128845230C>A | CA4475117 | FLNC | c.3765C>A (p.Val1255=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128845230C= | CA1742585444 | FLNC | c.3765C= (p.Val1255=) | |
| 7 | g.128845230C>G | CA4475118 | FLNC | c.3765C>G (p.Val1255=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128845230C>T | CA457579356 | FLNC | c.3765C>T (p.Val1255=) | |
| 7 | g.128845231T>A | CA369197976 | FLNC | c.3766T>A (p.Ser1256Thr) | |
| 7 | g.128845231T>C | CA369197978 | FLNC | c.3766T>C (p.Ser1256Pro) | gnomAD v4 |
| 7 | g.128845231T>G | CA369197979 | FLNC | c.3766T>G (p.Ser1256Ala) | |
| 7 | g.128845232C>A | CA369197982 | FLNC | c.3767C>A (p.Ser1256Ter) | |
| 7 | g.128845232C>G | CA369197987 | FLNC | c.3767C>G (p.Ser1256Ter) | |
| 7 | g.128845232C>T | CA369197988 | FLNC | c.3767C>T (p.Ser1256Leu) | dbSNP |
| 7 | g.128845233A>C | CA457579369 | FLNC | c.3768A>C (p.Ser1256=) | |
| 7 | g.128845233A>G | CA457579372 | FLNC | c.3768A>G (p.Ser1256=) | gnomAD v4 |
| 7 | g.128845233A>T | CA457579375 | FLNC | c.3768A>T (p.Ser1256=) | |
| 7 | g.128845234G>A | CA369197990 | FLNC | c.3769G>A (p.Gly1257Arg) | |
| 7 | g.128845234G>C | CA369197992 | FLNC | c.3769G>C (p.Gly1257Arg) | |
| 7 | g.128845234G>T | CA369197994 | FLNC | c.3769G>T (p.Gly1257Trp) | |
| 7 | g.128845235G>A | CA369198002 | FLNC | c.3770G>A (p.Gly1257Glu) | |
| 7 | g.128845235G>C | CA369198000 | FLNC | c.3770G>C (p.Gly1257Ala) | |
| 7 | g.128845235G>T | CA369197999 | FLNC | c.3770G>T (p.Gly1257Val) | |
| 7 | g.128845236G>A | CA4475119 | FLNC | c.3771G>A (p.Gly1257=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128845236G>C | CA457579385 | FLNC | c.3771G>C (p.Gly1257=) | |
| 7 | g.128845236G= | CA1742585452 | FLNC | c.3771G= (p.Gly1257=) | |
| 7 | g.128845236G>T | CA457579388 | FLNC | c.3771G>T (p.Gly1257=) | |
| 7 | g.128845237C>A | CA369198012 | FLNC | c.3772C>A (p.Pro1258Thr) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128845237C= | CA1742585460 | FLNC | c.3772C= (p.Pro1258=) | |
| 7 | g.128845237C>G | CA369198014 | FLNC | c.3772C>G (p.Pro1258Ala) | |
| 7 | g.128845237C>T | CA4475120 | FLNC | c.3772C>T (p.Pro1258Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128845238C>A | CA369198020 | FLNC | c.3773C>A (p.Pro1258His) | |
| 7 | g.128845238C= | CA1742585461 | FLNC | c.3773C= (p.Pro1258=) | |
| 7 | g.128845238C>G | CA369198022 | FLNC | c.3773C>G (p.Pro1258Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128845238C>T | CA369198025 | FLNC | c.3773C>T (p.Pro1258Leu) | gnomAD v4 |
| 7 | g.128845239T>A | CA457579403 | FLNC | c.3774T>A (p.Pro1258=) | gnomAD v4 |
| 7 | g.128845239T>C | CA457579407 | FLNC | c.3774T>C (p.Pro1258=) | |
| 7 | g.128845239T>G | CA457579405 | FLNC | c.3774T>G (p.Pro1258=) | |
| 7 | g.128845240G>A | CA369198028 | FLNC | c.3775G>A (p.Gly1259Ser) | |
| 7 | g.128845240G>C | CA369198031 | FLNC | c.3775G>C (p.Gly1259Arg) | |
| 7 | g.128845240G>T | CA369198033 | FLNC | c.3775G>T (p.Gly1259Cys) | |
| 7 | g.128845241G>A | CA369198036 | FLNC | c.3776G>A (p.Gly1259Asp) | |
| 7 | g.128845241G>C | CA369198039 | FLNC | c.3776G>C (p.Gly1259Ala) | |
| 7 | g.128845241G>T | CA369198042 | FLNC | c.3776G>T (p.Gly1259Val) | |
| 7 | g.128845242T>A | CA457579412 | FLNC | c.3777T>A (p.Gly1259=) | |
| 7 | g.128845242T>C | CA457579414 | FLNC | c.3777T>C (p.Gly1259=) | |
| 7 | g.128845242T>G | CA457579417 | FLNC | c.3777T>G (p.Gly1259=) | |
| 7 | g.128845243G>A | CA4475121 | FLNC | c.3778G>A (p.Val1260Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128845243G>C | CA369198046 | FLNC | c.3778G>C (p.Val1260Leu) | |
| 7 | g.128845243G= | CA1742585465 | FLNC | c.3778G= (p.Val1260=) | |
| 7 | g.128845243G>T | CA369198047 | FLNC | c.3778G>T (p.Val1260Phe) | |
| 7 | g.128845244T>A | CA369198052 | FLNC | c.3779T>A (p.Val1260Asp) | |
| 7 | g.128845244T>C | CA369198056 | FLNC | c.3779T>C (p.Val1260Ala) | |
| 7 | g.128845244T>G | CA369198058 | FLNC | c.3779T>G (p.Val1260Gly) |