| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128840028A= | CA1742545883 | FLNC | c.1417A= (p.Asn473=) | |
| 7 | g.128840028A>C | CA369225414 | FLNC | c.1417A>C (p.Asn473His) | |
| 7 | g.128840028A>G | CA4474339 | FLNC | c.1417A>G (p.Asn473Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840028A>T | CA369225415 | FLNC | c.1417A>T (p.Asn473Tyr) | |
| 7 | g.128840029A= | CA1742545884 | FLNC | c.1418A= (p.Asn473=) | |
| 7 | g.128840029A>C | CA369225417 | FLNC | c.1418A>C (p.Asn473Thr) | |
| 7 | g.128840029A>G | CA4474340 | FLNC | c.1418A>G (p.Asn473Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840029A>T | CA369225420 | FLNC | c.1418A>T (p.Asn473Ile) | |
| 7 | g.128840030C>A | CA4474341 | FLNC | c.1419C>A (p.Asn473Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128840030C= | CA1742545885 | FLNC | c.1419C= (p.Asn473=) | |
| 7 | g.128840030C>G | CA369225423 | FLNC | c.1419C>G (p.Asn473Lys) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128840030C>T | CA457582490 | FLNC | c.1419C>T (p.Asn473=) | gnomAD v4 |
| 7 | g.128840031C>A | CA369225425 | FLNC | c.1420C>A (p.Pro474Thr) | |
| 7 | g.128840031C= | CA1742545886 | FLNC | c.1420C= (p.Pro474=) | |
| 7 | g.128840031C>G | CA369225426 | FLNC | c.1420C>G (p.Pro474Ala) | |
| 7 | g.128840031C>T | CA369225427 | FLNC | c.1420C>T (p.Pro474Ser) | ClinVar dbSNP |
| 7 | g.128840032C>A | CA369225431 | FLNC | c.1421C>A (p.Pro474His) | |
| 7 | g.128840032C= | CA1742545887 | FLNC | c.1421C= (p.Pro474=) | |
| 7 | g.128840032C>G | CA369225429 | FLNC | c.1421C>G (p.Pro474Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128840032C>T | CA369225428 | FLNC | c.1421C>T (p.Pro474Leu) | |
| 7 | g.128840033C>A | CA457582494 | FLNC | c.1422C>A (p.Pro474=) | |
| 7 | g.128840033C>G | CA457582495 | FLNC | c.1422C>G (p.Pro474=) | |
| 7 | g.128840033C>T | CA457582496 | FLNC | c.1422C>T (p.Pro474=) | |
| 7 | g.128840034A>C | CA369225432 | FLNC | c.1423A>C (p.Asn475His) | |
| 7 | g.128840034A>G | CA369225434 | FLNC | c.1423A>G (p.Asn475Asp) | |
| 7 | g.128840034A>T | CA369225435 | FLNC | c.1423A>T (p.Asn475Tyr) | |
| 7 | g.128840035A>C | CA369225438 | FLNC | c.1424A>C (p.Asn475Thr) | |
| 7 | g.128840035A>G | CA369225440 | FLNC | c.1424A>G (p.Asn475Ser) | gnomAD v4 |
| 7 | g.128840035A>T | CA369225441 | FLNC | c.1424A>T (p.Asn475Ile) | |
| 7 | g.128840036C>A | CA369225445 | FLNC | c.1425C>A (p.Asn475Lys) | |
| 7 | g.128840036C= | CA1742545888 | FLNC | c.1425C= (p.Asn475=) | |
| 7 | g.128840036C>G | CA369225443 | FLNC | c.1425C>G (p.Asn475Lys) | |
| 7 | g.128840036C>T | CA4474342 | FLNC | c.1425C>T (p.Asn475=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840037G>A | CA166216016 | FLNC | c.1426G>A (p.Ala476Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128840037G>C | CA369225447 | FLNC | c.1426G>C (p.Ala476Pro) | |
| 7 | g.128840037G= | CA1742545889 | FLNC | c.1426G= (p.Ala476=) | |
| 7 | g.128840037G>T | CA4474343 | FLNC | c.1426G>T (p.Ala476Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840038C>A | CA369225451 | FLNC | c.1427C>A (p.Ala476Asp) | |
| 7 | g.128840038C= | CA1742545890 | FLNC | c.1427C= (p.Ala476=) | |
| 7 | g.128840038C>G | CA369225452 | FLNC | c.1427C>G (p.Ala476Gly) | |
| 7 | g.128840038C>T | CA369225453 | FLNC | c.1427C>T (p.Ala476Val) | dbSNP COSMIC |
| 7 | g.128840039C>A | CA457582505 | FLNC | c.1428C>A (p.Ala476=) | |
| 7 | g.128840039C= | CA1742545891 | FLNC | c.1428C= (p.Ala476=) | |
| 7 | g.128840039C>G | CA457582504 | FLNC | c.1428C>G (p.Ala476=) | dbSNP |
| 7 | g.128840039C>T | CA457582503 | FLNC | c.1428C>T (p.Ala476=) | ClinVar dbSNP |
| 7 | g.128840040T>A | CA369225455 | FLNC | c.1429T>A (p.Cys477Ser) | |
| 7 | g.128840040T>C | CA369225458 | FLNC | c.1429T>C (p.Cys477Arg) | dbSNP |
| 7 | g.128840040T>G | CA369225457 | FLNC | c.1429T>G (p.Cys477Gly) | |
| 7 | g.128840041G>A | CA369225460 | FLNC | c.1430G>A (p.Cys477Tyr) | |
| 7 | g.128840041G>C | CA4474344 | FLNC | c.1430G>C (p.Cys477Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |