| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128846787C>A | CA457581541 | FLNC | c.4170C>A (p.Pro1390=) | |
| 7 | g.128846787C= | CA1742588461 | FLNC | c.4170C= (p.Pro1390=) | |
| 7 | g.128846787C>G | CA457581544 | FLNC | c.4170C>G (p.Pro1390=) | |
| 7 | g.128846787C>T | CA4475267 | FLNC | c.4170C>T (p.Pro1390=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128846788_128846844del | CA2740094855 | FLNC | c.4171_4227del (p.Ser1391_Tyr1409del) | ClinVar |
| 7 | g.128846788T>A | CA369200490 | FLNC | c.4171T>A (p.Ser1391Thr) | |
| 7 | g.128846788T>C | CA369200492 | FLNC | c.4171T>C (p.Ser1391Pro) | dbSNP |
| 7 | g.128846788T>G | CA369200494 | FLNC | c.4171T>G (p.Ser1391Ala) | |
| 7 | g.128846788T= | CA1742588464 | FLNC | c.4171T= (p.Ser1391=) | |
| 7 | g.128846789C>A | CA369200496 | FLNC | c.4172C>A (p.Ser1391Ter) | ClinVar |
| 7 | g.128846789C= | CA1742588469 | FLNC | c.4172C= (p.Ser1391=) | |
| 7 | g.128846789C>G | CA369200497 | FLNC | c.4172C>G (p.Ser1391Trp) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128846789C>T | CA4475268 | FLNC | c.4172C>T (p.Ser1391Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128846790G>A | CA4475269 | FLNC | c.4173G>A (p.Ser1391=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128846790G>C | CA457581562 | FLNC | c.4173G>C (p.Ser1391=) | |
| 7 | g.128846790G= | CA1742588474 | FLNC | c.4173G= (p.Ser1391=) | |
| 7 | g.128846790G>T | CA457581564 | FLNC | c.4173G>T (p.Ser1391=) | |
| 7 | g.128846791G>A | CA369200506 | FLNC | c.4174G>A (p.Glu1392Lys) | |
| 7 | g.128846791G>C | CA369200504 | FLNC | c.4174G>C (p.Glu1392Gln) | |
| 7 | g.128846791G>T | CA369200503 | FLNC | c.4174G>T (p.Glu1392Ter) | |
| 7 | g.128846792A>C | CA369200509 | FLNC | c.4175A>C (p.Glu1392Ala) | |
| 7 | g.128846792A>G | CA369200510 | FLNC | c.4175A>G (p.Glu1392Gly) | |
| 7 | g.128846792A>T | CA369200512 | FLNC | c.4175A>T (p.Glu1392Val) | |
| 7 | g.128846793A= | CA1742588476 | FLNC | c.4176A= (p.Glu1392=) | |
| 7 | g.128846793A>C | CA369200514 | FLNC | c.4176A>C (p.Glu1392Asp) | ClinVar |
| 7 | g.128846793A>G | CA457581584 | FLNC | c.4176A>G (p.Glu1392=) | dbSNP |
| 7 | g.128846793A>T | CA369200516 | FLNC | c.4176A>T (p.Glu1392Asp) | |
| 7 | g.128846794G>A | CA369200518 | FLNC | c.4177G>A (p.Ala1393Thr) | |
| 7 | g.128846794G>C | CA369200520 | FLNC | c.4177G>C (p.Ala1393Pro) | |
| 7 | g.128846794G>T | CA369200522 | FLNC | c.4177G>T (p.Ala1393Ser) | |
| 7 | g.128846795C>A | CA369200523 | FLNC | c.4178C>A (p.Ala1393Asp) | COSMIC |
| 7 | g.128846795C= | CA1742588479 | FLNC | c.4178C= (p.Ala1393=) | |
| 7 | g.128846795C>G | CA369200525 | FLNC | c.4178C>G (p.Ala1393Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128846795C>T | CA369200526 | FLNC | c.4178C>T (p.Ala1393Val) | dbSNP |
| 7 | g.128846796C>A | CA457581607 | FLNC | c.4179C>A (p.Ala1393=) | |
| 7 | g.128846796C= | CA1742588481 | FLNC | c.4179C= (p.Ala1393=) | |
| 7 | g.128846796C>G | CA457581608 | FLNC | c.4179C>G (p.Ala1393=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128846796C>T | CA457581609 | FLNC | c.4179C>T (p.Ala1393=) | |
| 7 | g.128846797A= | CA1742588486 | FLNC | c.4180A= (p.Lys1394=) | |
| 7 | g.128846797A>C | CA369200528 | FLNC | c.4180A>C (p.Lys1394Gln) | |
| 7 | g.128846797A>G | CA369200530 | FLNC | c.4180A>G (p.Lys1394Glu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128846797A>T | CA369200531 | FLNC | c.4180A>T (p.Lys1394Ter) | |
| 7 | g.128846798A>C | CA369200537 | FLNC | c.4181A>C (p.Lys1394Thr) | ClinVar gnomAD v4 |
| 7 | g.128846798A>G | CA369200536 | FLNC | c.4181A>G (p.Lys1394Arg) | ClinVar |
| 7 | g.128846798A>T | CA369200534 | FLNC | c.4181A>T (p.Lys1394Met) | |
| 7 | g.128846799G>A | CA457581630 | FLNC | c.4182G>A (p.Lys1394=) | |
| 7 | g.128846799G>C | CA369200539 | FLNC | c.4182G>C (p.Lys1394Asn) | |
| 7 | g.128846799G>T | CA369200540 | FLNC | c.4182G>T (p.Lys1394Asn) | |
| 7 | g.128846800A>C | CA369200541 | FLNC | c.4183A>C (p.Met1395Leu) | |
| 7 | g.128846800A>G | CA369200542 | FLNC | c.4183A>G (p.Met1395Val) | gnomAD v4 COSMIC |