| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128837393C= | CA1742520728 | FLNC | c.700-5C= (n.700-5C=) | |
| 7 | g.128837393C>G | CA2715634627 | FLNC | c.700-5C>G (n.700-5C>G) | dbSNP |
| 7 | g.128837393C>T | CA4474110 | FLNC | c.700-5C>T (n.700-5C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128837394G>A | CA166214269 | FLNC | c.700-4G>A (n.700-4G>A) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128837394G= | CA1742520733 | FLNC | c.700-4G= (n.700-4G=) | |
| 7 | g.128837394G>T | CA4474111 | FLNC | c.700-4G>T (n.700-4G>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128837395C= | CA1742520741 | FLNC | c.700-3C= (n.700-3C=) | |
| 7 | g.128837395C>G | CA1107055734 | FLNC | c.700-3C>G (n.700-3C>G) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128837395C>T | CA2579013853 | FLNC | c.700-3C>T (n.700-3C>T) | |
| 7 | g.128837396A>C | CA369221790 | FLNC | c.700-2A>C (n.700-2A>C) | |
| 7 | g.128837396A>G | CA369221803 | FLNC | c.700-2A>G (n.700-2A>G) | ClinVar |
| 7 | g.128837396A>T | CA369221793 | FLNC | c.700-2A>T (n.700-2A>T) | |
| 7 | g.128837397G>A | CA369221806 | FLNC | c.700-1G>A (n.700-1G>A) | |
| 7 | g.128837397G>C | CA369221817 | FLNC | c.700-1G>C (n.700-1G>C) | |
| 7 | g.128837397G>T | CA369221808 | FLNC | c.700-1G>T (n.700-1G>T) | COSMIC |
| 7 | g.128837398G>A | CA369221821 | FLNC | c.700G>A (p.Val234Ile) | |
| 7 | g.128837398G>C | CA369221828 | FLNC | c.700G>C (p.Val234Leu) | |
| 7 | g.128837398G>T | CA369221825 | FLNC | c.700G>T (p.Val234Phe) | gnomAD v4 |
| 7 | g.128837399T>A | CA369221831 | FLNC | c.701T>A (p.Val234Asp) | |
| 7 | g.128837399T>C | CA369221844 | FLNC | c.701T>C (p.Val234Ala) | |
| 7 | g.128837399T>G | CA369221837 | FLNC | c.701T>G (p.Val234Gly) | ClinVar |
| 7 | g.128837400C>A | CA457846223 | FLNC | c.702C>A (p.Val234=) | |
| 7 | g.128837400C>G | CA457846224 | FLNC | c.702C>G (p.Val234=) | dbSNP |
| 7 | g.128837400C>T | CA457846225 | FLNC | c.702C>T (p.Val234=) | gnomAD v4 |
| 7 | g.128837401A>C | CA369221847 | FLNC | c.703A>C (p.Ile235Leu) | |
| 7 | g.128837401A>G | CA369221851 | FLNC | c.703A>G (p.Ile235Val) | |
| 7 | g.128837401A>T | CA369221848 | FLNC | c.703A>T (p.Ile235Phe) | |
| 7 | g.128837402T>A | CA369221858 | FLNC | c.704T>A (p.Ile235Asn) | |
| 7 | g.128837402T>C | CA369221863 | FLNC | c.704T>C (p.Ile235Thr) | |
| 7 | g.128837402T>G | CA369221861 | FLNC | c.704T>G (p.Ile235Ser) | |
| 7 | g.128837403T>A | CA457846228 | FLNC | c.705T>A (p.Ile235=) | |
| 7 | g.128837403T>C | CA457846230 | FLNC | c.705T>C (p.Ile235=) | dbSNP |
| 7 | g.128837403T>G | CA4474112 | FLNC | c.705T>G (p.Ile235Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128837403T= | CA1742520746 | FLNC | c.705T= (p.Ile235=) | |
| 7 | g.128837404G>A | CA369221869 | FLNC | c.706G>A (p.Ala236Thr) | dbSNP |
| 7 | g.128837404G>C | CA369221873 | FLNC | c.706G>C (p.Ala236Pro) | |
| 7 | g.128837404G= | CA1742520751 | FLNC | c.706G= (p.Ala236=) | |
| 7 | g.128837404G>T | CA369221875 | FLNC | c.706G>T (p.Ala236Ser) | |
| 7 | g.128837405C>A | CA369221878 | FLNC | c.707C>A (p.Ala236Asp) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128837405C= | CA1742520762 | FLNC | c.707C= (p.Ala236=) | |
| 7 | g.128837405C>G | CA369221879 | FLNC | c.707C>G (p.Ala236Gly) | |
| 7 | g.128837405C>T | CA166214283 | FLNC | c.707C>T (p.Ala236Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128837406C>A | CA457846231 | FLNC | c.708C>A (p.Ala236=) | |
| 7 | g.128837406C= | CA1742520769 | FLNC | c.708C= (p.Ala236=) | |
| 7 | g.128837406C>G | CA457846232 | FLNC | c.708C>G (p.Ala236=) | |
| 7 | g.128837406C>T | CA457846234 | FLNC | c.708C>T (p.Ala236=) | dbSNP |
| 7 | g.128837407C>A | CA369221882 | FLNC | c.709C>A (p.Pro237Thr) | |
| 7 | g.128837407C>G | CA369221884 | FLNC | c.709C>G (p.Pro237Ala) | |
| 7 | g.128837407C>T | CA369221892 | FLNC | c.709C>T (p.Pro237Ser) | |
| 7 | g.128837408C>A | CA369221895 | FLNC | c.710C>A (p.Pro237His) |