| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128841180C>A | CA457846581 | FLNC | c.1824C>A (p.Ile608=) | |
| 7 | g.128841180C= | CA1742568366 | FLNC | c.1824C= (p.Ile608=) | |
| 7 | g.128841180C>G | CA369227152 | FLNC | c.1824C>G (p.Ile608Met) | ClinVar dbSNP |
| 7 | g.128841180C>T | CA4474508 | FLNC | c.1824C>T (p.Ile608=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128841181G>A | CA4474509 | FLNC | c.1825G>A (p.Glu609Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128841181G>C | CA369227153 | FLNC | c.1825G>C (p.Glu609Gln) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128841181G= | CA1742568372 | FLNC | c.1825G= (p.Glu609=) | |
| 7 | g.128841181G>T | CA369227154 | FLNC | c.1825G>T (p.Glu609Ter) | |
| 7 | g.128841182del | CA2684812752 | FLNC | c.1826del (p.Glu609GlyfsTer?) | gnomAD v4 |
| 7 | g.128841182A>C | CA369227157 | FLNC | c.1826A>C (p.Glu609Ala) | |
| 7 | g.128841182A>G | CA369227156 | FLNC | c.1826A>G (p.Glu609Gly) | |
| 7 | g.128841182A>T | CA369227155 | FLNC | c.1826A>T (p.Glu609Val) | |
| 7 | g.128841183G>A | CA457846588 | FLNC | c.1827G>A (p.Glu609=) | COSMIC |
| 7 | g.128841183G>C | CA369227158 | FLNC | c.1827G>C (p.Glu609Asp) | |
| 7 | g.128841183G>T | CA369227159 | FLNC | c.1827G>T (p.Glu609Asp) | |
| 7 | g.128841186dup | CA2740097552 | FLNC | c.1830dup (p.Pro611AlafsTer9) | |
| 7 | g.128841184G>A | CA4474510 | FLNC | c.1828G>A (p.Gly610Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128841184G>C | CA369227160 | FLNC | c.1828G>C (p.Gly610Arg) | |
| 7 | g.128841184G= | CA1742568378 | FLNC | c.1828G= (p.Gly610=) | |
| 7 | g.128841184G>T | CA369227161 | FLNC | c.1828G>T (p.Gly610Trp) | |
| 7 | g.128841185G>A | CA369227162 | FLNC | c.1829G>A (p.Gly610Glu) | |
| 7 | g.128841185G>C | CA369227163 | FLNC | c.1829G>C (p.Gly610Ala) | |
| 7 | g.128841185G>T | CA369227164 | FLNC | c.1829G>T (p.Gly610Val) | |
| 7 | g.128841186G>A | CA457846590 | FLNC | c.1830G>A (p.Gly610=) | |
| 7 | g.128841186G>C | CA4474511 | FLNC | c.1830G>C (p.Gly610=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128841186G= | CA1742568385 | FLNC | c.1830G= (p.Gly610=) | |
| 7 | g.128841186G>T | CA457846592 | FLNC | c.1830G>T (p.Gly610=) | |
| 7 | g.128841187C>A | CA369227165 | FLNC | c.1831C>A (p.Pro611Thr) | |
| 7 | g.128841187C= | CA1742568389 | FLNC | c.1831C= (p.Pro611=) | |
| 7 | g.128841187C>G | CA369227166 | FLNC | c.1831C>G (p.Pro611Ala) | |
| 7 | g.128841187C>T | CA369227167 | FLNC | c.1831C>T (p.Pro611Ser) | dbSNP gnomAD v4 |
| 7 | g.128841188C>A | CA369227168 | FLNC | c.1832C>A (p.Pro611His) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128841188C= | CA1742568435 | FLNC | c.1832C= (p.Pro611=) | |
| 7 | g.128841188C>G | CA369227169 | FLNC | c.1832C>G (p.Pro611Arg) | |
| 7 | g.128841188C>T | CA369227170 | FLNC | c.1832C>T (p.Pro611Leu) | |
| 7 | g.128841189C>A | CA457846594 | FLNC | c.1833C>A (p.Pro611=) | |
| 7 | g.128841189C= | CA1742568453 | FLNC | c.1833C= (p.Pro611=) | |
| 7 | g.128841189C>G | CA457846593 | FLNC | c.1833C>G (p.Pro611=) | |
| 7 | g.128841189C>T | CA4474512 | FLNC | c.1833C>T (p.Pro611=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128841190T>A | CA369227171 | FLNC | c.1834T>A (p.Ser612Thr) | |
| 7 | g.128841190T>C | CA369227172 | FLNC | c.1834T>C (p.Ser612Pro) | |
| 7 | g.128841190T>G | CA369227173 | FLNC | c.1834T>G (p.Ser612Ala) | |
| 7 | g.128841191C>A | CA369227174 | FLNC | c.1835C>A (p.Ser612Ter) | |
| 7 | g.128841191C= | CA1742568461 | FLNC | c.1835C= (p.Ser612=) | |
| 7 | g.128841191C>G | CA369227175 | FLNC | c.1835C>G (p.Ser612Ter) | |
| 7 | g.128841191C>T | CA369227176 | FLNC | c.1835C>T (p.Ser612Leu) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128841192A= | CA1742568470 | FLNC | c.1836A= (p.Ser612=) | |
| 7 | g.128841192A>C | CA457846599 | FLNC | c.1836A>C (p.Ser612=) | dbSNP |
| 7 | g.128841192A>G | CA457846598 | FLNC | c.1836A>G (p.Ser612=) | |
| 7 | g.128841192A>T | CA457846597 | FLNC | c.1836A>T (p.Ser612=) |