| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128845018G>A | CA16605647 | FLNC | c.3553G>A (p.Glu1185Lys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128845018G>C | CA369197223 | FLNC | c.3553G>C (p.Glu1185Gln) | |
| 7 | g.128845018G= | CA1742584806 | FLNC | c.3553G= (p.Glu1185=) | |
| 7 | g.128845018G>T | CA369197224 | FLNC | c.3553G>T (p.Glu1185Ter) | |
| 7 | g.128845019A>C | CA369197225 | FLNC | c.3554A>C (p.Glu1185Ala) | |
| 7 | g.128845019A>G | CA369197226 | FLNC | c.3554A>G (p.Glu1185Gly) | |
| 7 | g.128845019A>T | CA369197227 | FLNC | c.3554A>T (p.Glu1185Val) | |
| 7 | g.128845020G>A | CA457848430 | FLNC | c.3555G>A (p.Glu1185=) | |
| 7 | g.128845020G>C | CA369197228 | FLNC | c.3555G>C (p.Glu1185Asp) | |
| 7 | g.128845020G>T | CA369197229 | FLNC | c.3555G>T (p.Glu1185Asp) | |
| 7 | g.128845021G>A | CA369197230 | FLNC | c.3556G>A (p.Ala1186Thr) | dbSNP gnomAD v4 |
| 7 | g.128845021G>C | CA369197231 | FLNC | c.3556G>C (p.Ala1186Pro) | |
| 7 | g.128845021G= | CA1742584816 | FLNC | c.3556G= (p.Ala1186=) | |
| 7 | g.128845021G>T | CA369197232 | FLNC | c.3556G>T (p.Ala1186Ser) | |
| 7 | g.128845022C>A | CA369197233 | FLNC | c.3557C>A (p.Ala1186Glu) | |
| 7 | g.128845022C= | CA1742584817 | FLNC | c.3557C= (p.Ala1186=) | |
| 7 | g.128845022C>G | CA369197235 | FLNC | c.3557C>G (p.Ala1186Gly) | |
| 7 | g.128845022C>T | CA369197234 | FLNC | c.3557C>T (p.Ala1186Val) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.128845023G>A | CA4475068 | FLNC | c.3558G>A (p.Ala1186=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128845023G>C | CA457848433 | FLNC | c.3558G>C (p.Ala1186=) | |
| 7 | g.128845023G= | CA1742584820 | FLNC | c.3558G= (p.Ala1186=) | |
| 7 | g.128845023G>T | CA457848431 | FLNC | c.3558G>T (p.Ala1186=) | dbSNP |
| 7 | g.128845024G>A | CA369197236 | FLNC | c.3559G>A (p.Glu1187Lys) | COSMIC |
| 7 | g.128845024G>C | CA369197237 | FLNC | c.3559G>C (p.Glu1187Gln) | |
| 7 | g.128845024G>T | CA369197238 | FLNC | c.3559G>T (p.Glu1187Ter) | |
| 7 | g.128845025A>C | CA369197239 | FLNC | c.3560A>C (p.Glu1187Ala) | |
| 7 | g.128845025A>G | CA369197241 | FLNC | c.3560A>G (p.Glu1187Gly) | |
| 7 | g.128845025A>T | CA369197240 | FLNC | c.3560A>T (p.Glu1187Val) | |
| 7 | g.128845026G>A | CA457848436 | FLNC | c.3561G>A (p.Glu1187=) | gnomAD v4 |
| 7 | g.128845026G>C | CA369197242 | FLNC | c.3561G>C (p.Glu1187Asp) | |
| 7 | g.128845026G>T | CA369197243 | FLNC | c.3561G>T (p.Glu1187Asp) | |
| 7 | g.128845027C>A | CA369197244 | FLNC | c.3562C>A (p.Leu1188Met) | |
| 7 | g.128845027C>G | CA369197245 | FLNC | c.3562C>G (p.Leu1188Val) | |
| 7 | g.128845027C>T | CA457848437 | FLNC | c.3562C>T (p.Leu1188=) | |
| 7 | g.128845028T>A | CA369197246 | FLNC | c.3563T>A (p.Leu1188Gln) | |
| 7 | g.128845028T>C | CA369197247 | FLNC | c.3563T>C (p.Leu1188Pro) | |
| 7 | g.128845028T>G | CA369197248 | FLNC | c.3563T>G (p.Leu1188Arg) | |
| 7 | g.128845029G>A | CA4475069 | FLNC | c.3564G>A (p.Leu1188=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.128845029G>C | CA457848439 | FLNC | c.3564G>C (p.Leu1188=) | |
| 7 | g.128845029G= | CA1742584825 | FLNC | c.3564G= (p.Leu1188=) | |
| 7 | g.128845029G>T | CA457848440 | FLNC | c.3564G>T (p.Leu1188=) | |
| 7 | g.128845030A>C | CA369197249 | FLNC | c.3565A>C (p.Thr1189Pro) | |
| 7 | g.128845030A>G | CA369197250 | FLNC | c.3565A>G (p.Thr1189Ala) | |
| 7 | g.128845030A>T | CA369197251 | FLNC | c.3565A>T (p.Thr1189Ser) | |
| 7 | g.128845031C>A | CA369197254 | FLNC | c.3566C>A (p.Thr1189Asn) | |
| 7 | g.128845031C>G | CA369197252 | FLNC | c.3566C>G (p.Thr1189Ser) | |
| 7 | g.128845031C>T | CA369197253 | FLNC | c.3566C>T (p.Thr1189Ile) | |
| 7 | g.128845032C>A | CA457848442 | FLNC | c.3567C>A (p.Thr1189=) | |
| 7 | g.128845032C>G | CA457848443 | FLNC | c.3567C>G (p.Thr1189=) | |
| 7 | g.128845032C>T | CA457848444 | FLNC | c.3567C>T (p.Thr1189=) |