| 7 | g.128843314G>A | CA4474795 | FLNC | c.2636G>A (p.Arg879His)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128843314G>C | CA369192636 | FLNC | c.2636G>C (p.Arg879Pro)
| |
| 7 | g.128843314G= | CA1742580450 | FLNC | c.2636G= (p.Arg879=)
| |
| 7 | g.128843314G>T | CA369192638 | FLNC | c.2636G>T (p.Arg879Leu)
| |
| 7 | g.128843315C>A | CA457577522 | FLNC | c.2637C>A (p.Arg879=)
| |
| 7 | g.128843315C>G | CA457577523 | FLNC | c.2637C>G (p.Arg879=)
| |
| 7 | g.128843315C>T | CA457577524 | FLNC | c.2637C>T (p.Arg879=)
| |
| 7 | g.128843317_128843318del | CA2579014200 | FLNC | c.2639_2640del (p.Thr880ArgfsTer?)
| |
| 7 | g.128843316A>C | CA369192640 | FLNC | c.2638A>C (p.Thr880Pro)
| |
| 7 | g.128843316A>G | CA369192643 | FLNC | c.2638A>G (p.Thr880Ala)
| |
| 7 | g.128843316A>T | CA369192642 | FLNC | c.2638A>T (p.Thr880Ser)
| |
| 7 | g.128843317C>A | CA369192647 | FLNC | c.2639C>A (p.Thr880Lys)
| |
| 7 | g.128843317C= | CA1742580451 | FLNC | c.2639C= (p.Thr880=)
| |
| 7 | g.128843317C>G | CA369192649 | FLNC | c.2639C>G (p.Thr880Arg)
| |
| 7 | g.128843317C>T | CA369192652 | FLNC | c.2639C>T (p.Thr880Ile)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128843318A= | CA1742580453 | FLNC | c.2640A= (p.Thr880=)
| |
| 7 | g.128843318A>C | CA457577525 | FLNC | c.2640A>C (p.Thr880=)
| dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128843318A>G | CA457577526 | FLNC | c.2640A>G (p.Thr880=)
| |
| 7 | g.128843318A>T | CA457577527 | FLNC | c.2640A>T (p.Thr880=)
| |
| 7 | g.128843319G>A | CA369192654 | FLNC | c.2641G>A (p.Gly881Ser)
| gnomAD v4 |
| 7 | g.128843319G>C | CA369192657 | FLNC | c.2641G>C (p.Gly881Arg)
| |
| 7 | g.128843319G>T | CA369192659 | FLNC | c.2641G>T (p.Gly881Cys)
| |
| 7 | g.128843320G>A | CA369192662 | FLNC | c.2641+1G>A (n.2641+1G>A)
| |
| 7 | g.128843320G>C | CA369192664 | FLNC | c.2641+1G>C (n.2641+1G>C)
| |
| 7 | g.128843320G>T | CA369192667 | FLNC | c.2641+1G>T (n.2641+1G>T)
| gnomAD v4 |
| 7 | g.128843321T>A | CA369192670 | FLNC | c.2641+2T>A (n.2641+2T>A)
| |
| 7 | g.128843321T>C | CA369192673 | FLNC | c.2641+2T>C (n.2641+2T>C)
| |
| 7 | g.128843321T>G | CA369192675 | FLNC | c.2641+2T>G (n.2641+2T>G)
| |
| 7 | g.128843321T= | CA1742580456 | FLNC | c.2641+2T= (n.2641+2T=)
| |
| 7 | g.128843323_128843338dup | CA833140203 | FLNC | c.2641+4_2641+19dup (n.2641+4_2641+19dup)
| dbSNP |
| 7 | g.128843324G>C | CA2573141716 | FLNC | c.2641+5G>C (n.2641+5G>C)
| ClinVar dbSNP gnomAD v4 |
| 7 | g.128843324G>T | CA2697557615 | FLNC | c.2641+5G>T (n.2641+5G>T)
| |
| 7 | g.128843324_128843328delinsGTGTC | CA1742580457 | FLNC | c.2641+5_2641+9delinsGTGTC (n.2641+5_2641+9delinsGTGTC)
| |
| 7 | g.128843325T>C | CA1107052831 | FLNC | c.2641+6T>C (n.2641+6T>C)
| dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128843325T= | CA1742580462 | FLNC | c.2641+6T= (n.2641+6T=)
| |
| 7 | g.128843327_128843330del | CA1742580461 | FLNC | c.2641+8_2641+11del (n.2641+8_2641+11del)
| ClinVar dbSNP |
| 7 | g.128843326G= | CA1742580464 | FLNC | c.2641+7G= (n.2641+7G=)
| |
| 7 | g.128843326G>T | CA4474796 | FLNC | c.2641+7G>T (n.2641+7G>T)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128843327T>C | CA578150955 | FLNC | c.2641+8T>C (n.2641+8T>C)
| dbSNP gnomAD v2 |
| 7 | g.128843327T= | CA1742580467 | FLNC | c.2641+8T= (n.2641+8T=)
| |
| 7 | g.128843328del | CA2684815864 | FLNC | c.2641+9del (n.2641+9del)
| gnomAD v4 |
| 7 | g.128843328C>A | CA1107052836 | FLNC | c.2641+9C>A (n.2641+9C>A)
| dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128843328C= | CA1742580471 | FLNC | c.2641+9C= (n.2641+9C=)
| |
| 7 | g.128843329T>C | CA2684815866 | FLNC | c.2641+10T>C (n.2641+10T>C)
| gnomAD v4 |
| 7 | g.128843331_128843332del | CA2684815867 | FLNC | c.2641+12_2641+13del (n.2641+12_2641+13del)
| gnomAD v4 |
| 7 | g.128843331G>A | CA578150957 | FLNC | c.2641+12G>A (n.2641+12G>A)
| dbSNP gnomAD v2 |
| 7 | g.128843331G= | CA1742580472 | FLNC | c.2641+12G= (n.2641+12G=)
| |
| 7 | g.128843336G>A | CA578150959 | FLNC | c.2641+17G>A (n.2641+17G>A)
| dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128843336G= | CA1742580474 | FLNC | c.2641+17G= (n.2641+17G=)
| |
| 7 | g.128843337G>A | CA4474797 | FLNC | c.2641+18G>A (n.2641+18G>A)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
