| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128845130G>A | CA369197594 | FLNC | c.3665G>A (p.Gly1222Asp) | |
| 7 | g.128845130G>C | CA369197596 | FLNC | c.3665G>C (p.Gly1222Ala) | |
| 7 | g.128845130G= | CA1742585126 | FLNC | c.3665G= (p.Gly1222=) | |
| 7 | g.128845130G>T | CA4475097 | FLNC | c.3665G>T (p.Gly1222Val) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.128845131C>A | CA457578839 | FLNC | c.3666C>A (p.Gly1222=) | |
| 7 | g.128845131C>G | CA457578840 | FLNC | c.3666C>G (p.Gly1222=) | |
| 7 | g.128845131C>T | CA457578842 | FLNC | c.3666C>T (p.Gly1222=) | gnomAD v4 |
| 7 | g.128845132A>C | CA369197600 | FLNC | c.3667A>C (p.Thr1223Pro) | |
| 7 | g.128845132A>G | CA369197602 | FLNC | c.3667A>G (p.Thr1223Ala) | |
| 7 | g.128845132A>T | CA369197604 | FLNC | c.3667A>T (p.Thr1223Ser) | |
| 7 | g.128845133C>A | CA369197606 | FLNC | c.3668C>A (p.Thr1223Asn) | |
| 7 | g.128845133C>G | CA369197610 | FLNC | c.3668C>G (p.Thr1223Ser) | |
| 7 | g.128845133C>T | CA369197608 | FLNC | c.3668C>T (p.Thr1223Ile) | |
| 7 | g.128845134C>A | CA457578849 | FLNC | c.3669C>A (p.Thr1223=) | |
| 7 | g.128845134C= | CA1742585129 | FLNC | c.3669C= (p.Thr1223=) | |
| 7 | g.128845134C>G | CA457578851 | FLNC | c.3669C>G (p.Thr1223=) | |
| 7 | g.128845134C>T | CA457578852 | FLNC | c.3669C>T (p.Thr1223=) | |
| 7 | g.128845135T>A | CA369197612 | FLNC | c.3670T>A (p.Tyr1224Asn) | dbSNP gnomAD v2 |
| 7 | g.128845135T>C | CA369197614 | FLNC | c.3670T>C (p.Tyr1224His) | |
| 7 | g.128845135T>G | CA369197615 | FLNC | c.3670T>G (p.Tyr1224Asp) | |
| 7 | g.128845135T= | CA1742585138 | FLNC | c.3670T= (p.Tyr1224=) | |
| 7 | g.128845135_128845136dup | CA1139660253 | FLNC | c.3670_3671dup (p.Ile1226ProfsTer?) | ClinVar dbSNP |
| 7 | g.128845136A>C | CA369197618 | FLNC | c.3671A>C (p.Tyr1224Ser) | |
| 7 | g.128845136A>G | CA369197619 | FLNC | c.3671A>G (p.Tyr1224Cys) | ClinVar |
| 7 | g.128845136A>T | CA369197621 | FLNC | c.3671A>T (p.Tyr1224Phe) | |
| 7 | g.128845137C>A | CA369197624 | FLNC | c.3672C>A (p.Tyr1224Ter) | |
| 7 | g.128845137C>G | CA369197625 | FLNC | c.3672C>G (p.Tyr1224Ter) | |
| 7 | g.128845137C>T | CA457578860 | FLNC | c.3672C>T (p.Tyr1224=) | |
| 7 | g.128845138A>C | CA369197628 | FLNC | c.3673A>C (p.Thr1225Pro) | |
| 7 | g.128845138A>G | CA369197629 | FLNC | c.3673A>G (p.Thr1225Ala) | |
| 7 | g.128845138A>T | CA369197631 | FLNC | c.3673A>T (p.Thr1225Ser) | |
| 7 | g.128845139C>A | CA369197637 | FLNC | c.3674C>A (p.Thr1225Asn) | dbSNP |
| 7 | g.128845139C= | CA1742585151 | FLNC | c.3674C= (p.Thr1225=) | |
| 7 | g.128845139C>G | CA369197635 | FLNC | c.3674C>G (p.Thr1225Ser) | |
| 7 | g.128845139C>T | CA369197634 | FLNC | c.3674C>T (p.Thr1225Ile) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128845140C>A | CA457578867 | FLNC | c.3675C>A (p.Thr1225=) | dbSNP gnomAD v2 |
| 7 | g.128845140C= | CA1742585154 | FLNC | c.3675C= (p.Thr1225=) | |
| 7 | g.128845140C>G | CA457578869 | FLNC | c.3675C>G (p.Thr1225=) | |
| 7 | g.128845140C>T | CA457578871 | FLNC | c.3675C>T (p.Thr1225=) | dbSNP |
| 7 | g.128845141A= | CA1742585157 | FLNC | c.3676A= (p.Ile1226=) | |
| 7 | g.128845141A>C | CA369197643 | FLNC | c.3676A>C (p.Ile1226Leu) | |
| 7 | g.128845141A>G | CA369197640 | FLNC | c.3676A>G (p.Ile1226Val) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128845141A>T | CA369197642 | FLNC | c.3676A>T (p.Ile1226Phe) | |
| 7 | g.128845142T>A | CA369197645 | FLNC | c.3677T>A (p.Ile1226Asn) | |
| 7 | g.128845142T>C | CA369197647 | FLNC | c.3677T>C (p.Ile1226Thr) | |
| 7 | g.128845142T>G | CA369197649 | FLNC | c.3677T>G (p.Ile1226Ser) | |
| 7 | g.128845143T>A | CA457578877 | FLNC | c.3678T>A (p.Ile1226=) | |
| 7 | g.128845143T>C | CA457578879 | FLNC | c.3678T>C (p.Ile1226=) | |
| 7 | g.128845143T>G | CA369197651 | FLNC | c.3678T>G (p.Ile1226Met) | |
| 7 | g.128845143T= | CA1742585160 | FLNC | c.3678T= (p.Ile1226=) |