UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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 |
| 7 | g.128840041G= | CA1742545892 | FLNC | c.1430G= (p.Cys477=) | |
| 7 | g.128840041G>T | CA369225463 | FLNC | c.1430G>T (p.Cys477Phe) | gnomAD v4 |
| 7 | g.128840041_128840042delinsGC | CA1742545893 | FLNC | c.1430_1431delinsGC (p.Cys477=) | |
| 7 | g.128840042C>A | CA369225465 | FLNC | c.1431C>A (p.Cys477Ter) | |
| 7 | g.128840042C>G | CA369225467 | FLNC | c.1431C>G (p.Cys477Trp) | |
| 7 | g.128840042C>T | CA457582509 | FLNC | c.1431C>T (p.Cys477=) | |
| 7 | g.128840043del | CA833136008 | FLNC | c.1432del (p.Arg478AlafsTer14) | dbSNP |
| 7 | g.128840043C>A | CA369225469 | FLNC | c.1432C>A (p.Arg478Ser) | |
| 7 | g.128840043C= | CA1742545894 | FLNC | c.1432C= (p.Arg478=) | |
| 7 | g.128840043C>G | CA369225472 | FLNC | c.1432C>G (p.Arg478Gly) | |
| 7 | g.128840043C>T | CA4474345 | FLNC | c.1432C>T (p.Arg478Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840044G>A | CA4474346 | FLNC | c.1433G>A (p.Arg478His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840044G>C | CA369225476 | FLNC | c.1433G>C (p.Arg478Pro) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128840044G= | CA1742545895 | FLNC | c.1433G= (p.Arg478=) | |
| 7 | g.128840044G>T | CA369225478 | FLNC | c.1433G>T (p.Arg478Leu) | dbSNP |
| 7 | g.128840045C>A | CA457582513 | FLNC | c.1434C>A (p.Arg478=) | |
| 7 | g.128840045C= | CA1742545896 | FLNC | c.1434C= (p.Arg478=) | |
| 7 | g.128840045C>G | CA457582514 | FLNC | c.1434C>G (p.Arg478=) | |
| 7 | g.128840045C>T | CA4474347 | FLNC | c.1434C>T (p.Arg478=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840046G>A | CA4474348 | FLNC | c.1435G>A (p.Ala479Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840046G>C | CA369225481 | FLNC | c.1435G>C (p.Ala479Pro) | dbSNP gnomAD v2 COSMIC |
| 7 | g.128840046G= | CA1742545897 | FLNC | c.1435G= (p.Ala479=) | |
| 7 | g.128840046G>T | CA369225483 | FLNC | c.1435G>T (p.Ala479Ser) | |
| 7 | g.128840047C>A | CA369225487 | FLNC | c.1436C>A (p.Ala479Asp) | |
| 7 | g.128840047C= | CA1742545898 | FLNC | c.1436C= (p.Ala479=) | |
| 7 | g.128840047C>G | CA369225489 | FLNC | c.1436C>G (p.Ala479Gly) | |
| 7 | g.128840047C>T | CA369225490 | FLNC | c.1436C>T (p.Ala479Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840048C>A | CA457582519 | FLNC | c.1437C>A (p.Ala479=) | |
| 7 | g.128840048C= | CA1742545899 | FLNC | c.1437C= (p.Ala479=) | |
| 7 | g.128840048C>G | CA457582518 | FLNC | c.1437C>G (p.Ala479=) | |
| 7 | g.128840048C>T | CA4474349 | FLNC | c.1437C>T (p.Ala479=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840049T>A | CA369225494 | FLNC | c.1438T>A (p.Ser480Thr) | |
| 7 | g.128840049T>C | CA369225496 | FLNC | c.1438T>C (p.Ser480Pro) | ClinVar |
| 7 | g.128840049T>G | CA369225497 | FLNC | c.1438T>G (p.Ser480Ala) | |
| 7 | g.128840050C>A | CA369225498 | FLNC | c.1439C>A (p.Ser480Tyr) | |
| 7 | g.128840050C>G | CA369225499 | FLNC | c.1439C>G (p.Ser480Cys) | |
| 7 | g.128840050C>T | CA369225501 | FLNC | c.1439C>T (p.Ser480Phe) | |
| 7 | g.128840051T>A | CA457582521 | FLNC | c.1440T>A (p.Ser480=) | |
| 7 | g.128840051T>C | CA457582523 | FLNC | c.1440T>C (p.Ser480=) | |
| 7 | g.128840051T>G | CA457582522 | FLNC | c.1440T>G (p.Ser480=) | |
| 7 | g.128840052G>A | CA369225503 | FLNC | c.1441G>A (p.Gly481Arg) | gnomAD v4 |
| 7 | g.128840052G>C | CA369225505 | FLNC | c.1441G>C (p.Gly481Arg) | |
| 7 | g.128840052G>T | CA369225507 | FLNC | c.1441G>T (p.Gly481Trp) | |
| 7 | g.128840053G>A | CA369225513 | FLNC | c.1442G>A (p.Gly481Glu) | |
| 7 | g.128840053G>C | CA369225511 | FLNC | c.1442G>C (p.Gly481Ala) | gnomAD v4 |
| 7 | g.128840053G>T | CA369225509 | FLNC | c.1442G>T (p.Gly481Val) | |
| 7 | g.128840054G>A | CA457582526 | FLNC | c.1443G>A (p.Gly481=) | |
| 7 | g.128840054G>C | CA457582527 | FLNC | c.1443G>C (p.Gly481=) | |
| 7 | g.128840054G>T | CA457582528 | FLNC | c.1443G>T (p.Gly481=) | |
| 7 | g.128840055C>A | CA457582529 | FLNC | c.1444C>A (p.Arg482=) | |
| 7 | g.128840055C= | CA1742545900 | FLNC | c.1444C= (p.Arg482=) | |
| 7 | g.128840055C>G | CA369225514 | FLNC | c.1444C>G (p.Arg482Gly) | |
| 7 | g.128840055C>T | CA369225516 | FLNC | c.1444C>T (p.Arg482Ter) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128840056G>A | CA4474350 | FLNC | c.1445G>A (p.Arg482Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128840056G>C | CA369225518 | FLNC | c.1445G>C (p.Arg482Pro) | |
| 7 | g.128840056G= | CA1742545901 | FLNC | c.1445G= (p.Arg482=) | |
| 7 | g.128840056G>T | CA369225521 | FLNC | c.1445G>T (p.Arg482Leu) | |
| 7 | g.128840057A>C | CA457582533 | FLNC | c.1446A>C (p.Arg482=) | |
| 7 | g.128840057A>G | CA457582534 | FLNC | c.1446A>G (p.Arg482=) | |
| 7 | g.128840057A>T | CA457582535 | FLNC | c.1446A>T (p.Arg482=) | |
| 7 | g.128840058G>A | CA369225523 | FLNC | c.1447G>A (p.Gly483Ser) | |
| 7 | g.128840058G>C | CA369225525 | FLNC | c.1447G>C (p.Gly483Arg) | |
| 7 | g.128840058G>T | CA369225527 | FLNC | c.1447G>T (p.Gly483Cys) | |
| 7 | g.128840059G>A | CA369225530 | FLNC | c.1448G>A (p.Gly483Asp) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128840059G>C | CA369225531 | FLNC | c.1448G>C (p.Gly483Ala) | gnomAD v4 |
| 7 | g.128840059G= | CA1742545902 | FLNC | c.1448G= (p.Gly483=) | |
| 7 | g.128840059G>T | CA369225533 | FLNC | c.1448G>T (p.Gly483Val) | |
| 7 | g.128840060C>A | CA457582537 | FLNC | c.1449C>A (p.Gly483=) | |
| 7 | g.128840060C>G | CA457582538 | FLNC | c.1449C>G (p.Gly483=) | ClinVar |
| 7 | g.128840060C>T | CA457582539 | FLNC | c.1449C>T (p.Gly483=) | |
| 7 | g.128840061C>A | CA369225535 | FLNC | c.1450C>A (p.Leu484Met) | |
| 7 | g.128840061C= | CA1742545903 | FLNC | c.1450C= (p.Leu484=) | |
| 7 | g.128840061C>G | CA369225544 | FLNC | c.1450C>G (p.Leu484Val) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128840061C>T | CA457582540 | FLNC | c.1450C>T (p.Leu484=) | |
| 7 | g.128840062T>A | CA369225547 | FLNC | c.1451T>A (p.Leu484Gln) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128840062T>C | CA369225549 | FLNC | c.1451T>C (p.Leu484Pro) | gnomAD v4 |
| 7 | g.128840062T>G | CA369225545 | FLNC | c.1451T>G (p.Leu484Arg) | |
| 7 | g.128840062T= | CA1742545904 | FLNC | c.1451T= (p.Leu484=) | |
| 7 | g.128840063G>A | CA457582545 | FLNC | c.1452G>A (p.Leu484=) | dbSNP |
| 7 | g.128840063G>C | CA457582546 | FLNC | c.1452G>C (p.Leu484=) | |
| 7 | g.128840063G= | CA1742545905 | FLNC | c.1452G= (p.Leu484=) | |
| 7 | g.128840063G>T | CA457582547 | FLNC | c.1452G>T (p.Leu484=) | |
| 7 | g.128840064C>A | CA369225551 | FLNC | c.1453C>A (p.Gln485Lys) | |
| 7 | g.128840064C>G | CA369225553 | FLNC | c.1453C>G (p.Gln485Glu) | |
| 7 | g.128840064C>T | CA369225552 | FLNC | c.1453C>T (p.Gln485Ter) | ClinVar gnomAD v4 |
| 7 | g.128840065A= | CA1742545906 | FLNC | c.1454A= (p.Gln485=) | |
| 7 | g.128840065A>C | CA369225555 | FLNC | c.1454A>C (p.Gln485Pro) | |
| 7 | g.128840065A>G | CA166216071 | FLNC | c.1454A>G (p.Gln485Arg) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128840065A>T | CA369225557 | FLNC | c.1454A>T (p.Gln485Leu) | |
| 7 | g.128840066G>A | CA457582550 | FLNC | c.1455G>A (p.Gln485=) | |
| 7 | g.128840066G>C | CA369225559 | FLNC | c.1455G>C (p.Gln485His) | |
| 7 | g.128840066G>T | CA369225560 | FLNC | c.1455G>T (p.Gln485His) | |
| 7 | g.128840067C>A | CA369225561 | FLNC | c.1456C>A (p.Pro486Thr) | |
| 7 | g.128840067C= | CA1742545907 | FLNC | c.1456C= (p.Pro486=) | |
| 7 | g.128840067C>G | CA369225562 | FLNC | c.1456C>G (p.Pro486Ala) | |
| 7 | g.128840067C>T | CA369225563 | FLNC | c.1456C>T (p.Pro486Ser) | dbSNP |
| 7 | g.128840067_128840069delinsTCA | CA2573052814 | FLNC | c.1456_1458delinsTCA (p.Pro486Ser) | ClinVar dbSNP |
| 7 | g.128840068C>A | CA369225565 | FLNC | c.1457C>A (p.Pro486His) | |
| 7 | g.128840068C>G | CA369225567 | FLNC | c.1457C>G (p.Pro486Arg) | |
| 7 | g.128840068C>T | CA369225569 | FLNC | c.1457C>T (p.Pro486Leu) | |
| 7 | g.128840069C>A | CA152832 | FLNC | c.1458C>A (p.Pro486=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840069C= | CA1742545908 | FLNC | c.1458C= (p.Pro486=) | |
| 7 | g.128840069C>G | CA457582553 | FLNC | c.1458C>G (p.Pro486=) | COSMIC |
| 7 | g.128840069C>T | CA457582555 | FLNC | c.1458C>T (p.Pro486=) | gnomAD v4 |
| 7 | g.128840070A= | CA1742545909 | FLNC | c.1459A= (p.Lys487=) | |
| 7 | g.128840070A>C | CA369225573 | FLNC | c.1459A>C (p.Lys487Gln) | dbSNP |
| 7 | g.128840070A>G | CA369225578 | FLNC | c.1459A>G (p.Lys487Glu) | |
| 7 | g.128840070A>T | CA369225575 | FLNC | c.1459A>T (p.Lys487Ter) | |
| 7 | g.128840071A>C | CA369225580 | FLNC | c.1460A>C (p.Lys487Thr) | |
| 7 | g.128840071A>G | CA369225582 | FLNC | c.1460A>G (p.Lys487Arg) | gnomAD v4 |
| 7 | g.128840071A>T | CA369225584 | FLNC | c.1460A>T (p.Lys487Met) | |
| 7 | g.128840072G>A | CA4474351 | FLNC | c.1461G>A (p.Lys487=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128840072G>C | CA369225587 | FLNC | c.1461G>C (p.Lys487Asn) | |
| 7 | g.128840072G= | CA1742545910 | FLNC | c.1461G= (p.Lys487=) | |
| 7 | g.128840072G>T | CA369225588 | FLNC | c.1461G>T (p.Lys487Asn) | COSMIC |
| 7 | g.128840074del | CA2573141702 | FLNC | c.1463del (p.Gly488ValfsTer4) | ClinVar dbSNP |
| 7 | g.128840073G>A | CA369225590 | FLNC | c.1462G>A (p.Gly488Ser) | ClinVar |
| 7 | g.128840073G>C | CA369225591 | FLNC | c.1462G>C (p.Gly488Arg) | |
| 7 | g.128840073G= | CA1742545911 | FLNC | c.1462G= (p.Gly488=) | |
| 7 | g.128840073G>T | CA369225593 | FLNC | c.1462G>T (p.Gly488Cys) | dbSNP |
| 7 | g.128840074G>A | CA369225597 | FLNC | c.1463G>A (p.Gly488Asp) | |
| 7 | g.128840074G>C | CA369225599 | FLNC | c.1463G>C (p.Gly488Ala) | |
| 7 | g.128840074G>T | CA369225595 | FLNC | c.1463G>T (p.Gly488Val) | gnomAD v4 |
| 7 | g.128840075T>A | CA457582561 | FLNC | c.1464T>A (p.Gly488=) | |
| 7 | g.128840075T>C | CA457582563 | FLNC | c.1464T>C (p.Gly488=) | |
| 7 | g.128840075T>G | CA457582565 | FLNC | c.1464T>G (p.Gly488=) | |
| 7 | g.128840076G>A | CA369225601 | FLNC | c.1465G>A (p.Val489Ile) | gnomAD v4 COSMIC |
| 7 | g.128840076G>C | CA369225603 | FLNC | c.1465G>C (p.Val489Leu) | |
| 7 | g.128840076G>T | CA369225605 | FLNC | c.1465G>T (p.Val489Phe) | |
| 7 | g.128840077T>A | CA369225606 | FLNC | c.1466T>A (p.Val489Asp) | |
| 7 | g.128840077T>C | CA369225607 | FLNC | c.1466T>C (p.Val489Ala) | |
| 7 | g.128840077T>G | CA369225608 | FLNC | c.1466T>G (p.Val489Gly) | |
| 7 | g.128840077_128840083del | CA2695208474 | FLNC | c.1466_1472del (p.Val489GlyfsTer?) | |
| 7 | g.128840077_128840084delinsA | CA2695208475 | FLNC | c.1466_1473delinsA (p.Val489GlufsTer?) | |
| 7 | g.128840078T>A | CA457582567 | FLNC | c.1467T>A (p.Val489=) | |
| 7 | g.128840078T>C | CA457582568 | FLNC | c.1467T>C (p.Val489=) | |
| 7 | g.128840078T>G | CA457582569 | FLNC | c.1467T>G (p.Val489=) | |
| 7 | g.128840079C>A | CA369225609 | FLNC | c.1468C>A (p.Arg490Ser) | gnomAD v4 |
| 7 | g.128840079C= | CA1742545912 | FLNC | c.1468C= (p.Arg490=) | |
| 7 | g.128840079C>G | CA369225614 | FLNC | c.1468C>G (p.Arg490Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128840079C>T | CA369225616 | FLNC | c.1468C>T (p.Arg490Cys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128840080G>A | CA166216085 | FLNC | c.1469G>A (p.Arg490His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840080G>C | CA369225618 | FLNC | c.1469G>C (p.Arg490Pro) | |
| 7 | g.128840080G= | CA1742545913 | FLNC | c.1469G= (p.Arg490=) | |
| 7 | g.128840080G>T | CA369225620 | FLNC | c.1469G>T (p.Arg490Leu) | ClinVar dbSNP gnomAD v2 |
| 7 | g.128840081C>A | CA457582581 | FLNC | c.1470C>A (p.Arg490=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128840081C= | CA1742545914 | FLNC | c.1470C= (p.Arg490=) | |
| 7 | g.128840081C>G | CA457582577 | FLNC | c.1470C>G (p.Arg490=) | gnomAD v4 |
| 7 | g.128840081C>T | CA4474352 | FLNC | c.1470C>T (p.Arg490=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840082G>A | CA4474353 | FLNC | c.1471G>A (p.Val491Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840082G>C | CA10576718 | FLNC | c.1471G>C (p.Val491Leu) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.128840082G= | CA1742545915 | FLNC | c.1471G= (p.Val491=) | |
| 7 | g.128840082G>T | CA4474354 | FLNC | c.1471G>T (p.Val491Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840083T>A | CA369225630 | FLNC | c.1472T>A (p.Val491Glu) | ClinVar gnomAD v4 |
| 7 | g.128840083T>C | CA369225633 | FLNC | c.1472T>C (p.Val491Ala) | |
| 7 | g.128840083T>G | CA369225635 | FLNC | c.1472T>G (p.Val491Gly) | |
| 7 | g.128840084G>A | CA457582585 | FLNC | c.1473G>A (p.Val491=) | |
| 7 | g.128840084G>C | CA457582587 | FLNC | c.1473G>C (p.Val491=) | gnomAD v4 |
| 7 | g.128840084G>T | CA457582589 | FLNC | c.1473G>T (p.Val491=) | |
| 7 | g.128840085A= | CA1742545916 | FLNC | c.1474A= (p.Lys492=) | |
| 7 | g.128840085A>C | CA369225639 | FLNC | c.1474A>C (p.Lys492Gln) | |
| 7 | g.128840085A>G | CA4474355 | FLNC | c.1474A>G (p.Lys492Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840085A>T | CA369225642 | FLNC | c.1474A>T (p.Lys492Ter) | |
| 7 | g.128840087dup | CA2684820207 | FLNC | c.1476dup (p.Glu493ArgfsTer4) | gnomAD v4 |
| 7 | g.128840086A= | CA1742545917 | FLNC | c.1475A= (p.Lys492=) | |
| 7 | g.128840086A>C | CA4474356 | FLNC | c.1475A>C (p.Lys492Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128840086A>G | CA369225644 | FLNC | c.1475A>G (p.Lys492Arg) | |
| 7 | g.128840086A>T | CA369225645 | FLNC | c.1475A>T (p.Lys492Ile) | |
| 7 | g.128840087A= | CA1742545918 | FLNC | c.1476A= (p.Lys492=) | |
| 7 | g.128840087A>C | CA369225647 | FLNC | c.1476A>C (p.Lys492Asn) | |
| 7 | g.128840087A>G | CA4474357 | FLNC | c.1476A>G (p.Lys492=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128840087A>T | CA369225649 | FLNC | c.1476A>T (p.Lys492Asn) | |
| 7 | g.128840088G>A | CA369225654 | FLNC | c.1477G>A (p.Glu493Lys) | gnomAD v4 COSMIC |
| 7 | g.128840088G>C | CA369225653 | FLNC | c.1477G>C (p.Glu493Gln) | |
| 7 | g.128840088G>T | CA369225651 | FLNC | c.1477G>T (p.Glu493Ter) | |
| 7 | g.128840089A>C | CA369225657 | FLNC | c.1478A>C (p.Glu493Ala) | |
| 7 | g.128840089A>G | CA369225661 | FLNC | c.1478A>G (p.Glu493Gly) | |
| 7 | g.128840089A>T | CA369225659 | FLNC | c.1478A>T (p.Glu493Val) | |
| 7 | g.128840090G>A | CA457582595 | FLNC | c.1479G>A (p.Glu493=) | |
| 7 | g.128840090G>C | CA369225663 | FLNC | c.1479G>C (p.Glu493Asp) | |
| 7 | g.128840090G>T | CA369225664 | FLNC | c.1479G>T (p.Glu493Asp) | |
| 7 | g.128840091G>A | CA369225666 | FLNC | c.1480G>A (p.Val494Met) | |
| 7 | g.128840091G>C | CA369225667 | FLNC | c.1480G>C (p.Val494Leu) | |
| 7 | g.128840091G>T | CA369225669 | FLNC | c.1480G>T (p.Val494Leu) | |
| 7 | g.128840092T>A | CA369225675 | FLNC | c.1481T>A (p.Val494Glu) | |
| 7 | g.128840092T>C | CA369225673 | FLNC | c.1481T>C (p.Val494Ala) | |
| 7 | g.128840092T>G | CA369225672 | FLNC | c.1481T>G (p.Val494Gly) | |
| 7 | g.128840093G>A | CA457582600 | FLNC | c.1482G>A (p.Val494=) | gnomAD v4 |
| 7 | g.128840093G>C | CA457582601 | FLNC | c.1482G>C (p.Val494=) | |
| 7 | g.128840093G>T | CA457582603 | FLNC | c.1482G>T (p.Val494=) | |
| 7 | g.128840094G>A | CA369225676 | FLNC | c.1483G>A (p.Ala495Thr) | |
| 7 | g.128840094G>C | CA369225677 | FLNC | c.1483G>C (p.Ala495Pro) | |
| 7 | g.128840094G>T | CA369225678 | FLNC | c.1483G>T (p.Ala495Ser) | |
| 7 | g.128840095C>A | CA369225680 | FLNC | c.1484C>A (p.Ala495Asp) | |
| 7 | g.128840095C>G | CA369225681 | FLNC | c.1484C>G (p.Ala495Gly) | ClinVar |
| 7 | g.128840095C>T | CA369225683 | FLNC | c.1484C>T (p.Ala495Val) | ClinVar |
| 7 | g.128840096T>A | CA457582612 | FLNC | c.1485T>A (p.Ala495=) | |
| 7 | g.128840096T>C | CA457582614 | FLNC | c.1485T>C (p.Ala495=) | ClinVar dbSNP |
| 7 | g.128840096T>G | CA457582615 | FLNC | c.1485T>G (p.Ala495=) | dbSNP gnomAD v2 |
| 7 | g.128840096T= | CA1742545919 | FLNC | c.1485T= (p.Ala495=) | |
| 7 | g.128840097G>A | CA369225686 | FLNC | c.1486G>A (p.Asp496Asn) | |
| 7 | g.128840097G>C | CA369225684 | FLNC | c.1486G>C (p.Asp496His) | |
| 7 | g.128840097G>T | CA369225685 | FLNC | c.1486G>T (p.Asp496Tyr) | |
| 7 | g.128840098A>C | CA369225687 | FLNC | c.1487A>C (p.Asp496Ala) | |
| 7 | g.128840098A>G | CA369225689 | FLNC | c.1487A>G (p.Asp496Gly) | |
| 7 | g.128840098A>T | CA369225691 | FLNC | c.1487A>T (p.Asp496Val) | |
| 7 | g.128840099C>A | CA369225692 | FLNC | c.1488C>A (p.Asp496Glu) | |
| 7 | g.128840099C= | CA1742545920 | FLNC | c.1488C= (p.Asp496=) | |
| 7 | g.128840099C>G | CA369225694 | FLNC | c.1488C>G (p.Asp496Glu) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128840099C>T | CA457582632 | FLNC | c.1488C>T (p.Asp496=) | |
| 7 | g.128840100T>A | CA369225696 | FLNC | c.1489T>A (p.Phe497Ile) | |
| 7 | g.128840100T>C | CA369225698 | FLNC | c.1489T>C (p.Phe497Leu) | COSMIC |
| 7 | g.128840100T>G | CA369225700 | FLNC | c.1489T>G (p.Phe497Val) | |
| 7 | g.128840101T>A | CA369225702 | FLNC | c.1490T>A (p.Phe497Tyr) | |
| 7 | g.128840101T>C | CA369225705 | FLNC | c.1490T>C (p.Phe497Ser) | |
| 7 | g.128840101T>G | CA369225707 | FLNC | c.1490T>G (p.Phe497Cys) | |
| 7 | g.128840102C>A | CA369225708 | FLNC | c.1491C>A (p.Phe497Leu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128840102C= | CA1742545921 | FLNC | c.1491C= (p.Phe497=) | |
| 7 | g.128840102C>G | CA369225710 | FLNC | c.1491C>G (p.Phe497Leu) | |
| 7 | g.128840102C>T | CA457582650 | FLNC | c.1491C>T (p.Phe497=) | ClinVar dbSNP |
| 7 | g.128840103A= | CA1742545922 | FLNC | c.1492A= (p.Lys498=) | |
| 7 | g.128840103A>C | CA369225714 | FLNC | c.1492A>C (p.Lys498Gln) | |
| 7 | g.128840103A>G | CA4474358 | FLNC | c.1492A>G (p.Lys498Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840103A>T | CA369225713 | FLNC | c.1492A>T (p.Lys498Ter) | |
| 7 | g.128840104A>C | CA369225717 | FLNC | c.1493A>C (p.Lys498Thr) | |
| 7 | g.128840104A>G | CA369225719 | FLNC | c.1493A>G (p.Lys498Arg) | |
| 7 | g.128840104A>T | CA369225720 | FLNC | c.1493A>T (p.Lys498Met) | |
| 7 | g.128840105G>A | CA457582666 | FLNC | c.1494G>A (p.Lys498=) | ClinVar dbSNP |
| 7 | g.128840105G>C | CA369225722 | FLNC | c.1494G>C (p.Lys498Asn) | |
| 7 | g.128840105G= | CA1742545923 | FLNC | c.1494G= (p.Lys498=) | |
| 7 | g.128840105G>T | CA369225723 | FLNC | c.1494G>T (p.Lys498Asn) | |
| 7 | g.128840106G>A | CA4474359 | FLNC | c.1495G>A (p.Val499Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840106G>C | CA369225725 | FLNC | c.1495G>C (p.Val499Leu) | |
| 7 | g.128840106G= | CA1742545924 | FLNC | c.1495G= (p.Val499=) | |
| 7 | g.128840106G>T | CA369225724 | FLNC | c.1495G>T (p.Val499Leu) | |
| 7 | g.128840107T>A | CA369225726 | FLNC | c.1496T>A (p.Val499Glu) | |
| 7 | g.128840107T>C | CA369225727 | FLNC | c.1496T>C (p.Val499Ala) | |
| 7 | g.128840107T>G | CA369225728 | FLNC | c.1496T>G (p.Val499Gly) | |
| 7 | g.128840108del | CA2580076616 | FLNC | c.1497del (p.Phe500LeufsTer24) | ClinVar |
| 7 | g.128840108G>A | CA457582678 | FLNC | c.1497G>A (p.Val499=) | gnomAD v4 |
| 7 | g.128840108G>C | CA457582683 | FLNC | c.1497G>C (p.Val499=) | |
| 7 | g.128840108G>T | CA457582685 | FLNC | c.1497G>T (p.Val499=) | gnomAD v4 |
| 7 | g.128840109T>A | CA369225729 | FLNC | c.1498T>A (p.Phe500Ile) | |
| 7 | g.128840109T>C | CA369225730 | FLNC | c.1498T>C (p.Phe500Leu) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128840109T>G | CA369225731 | FLNC | c.1498T>G (p.Phe500Val) | |
| 7 | g.128840109T= | CA1742545925 | FLNC | c.1498T= (p.Phe500=) | |
| 7 | g.128840110T>A | CA369225737 | FLNC | c.1499T>A (p.Phe500Tyr) | |
| 7 | g.128840110T>C | CA369225734 | FLNC | c.1499T>C (p.Phe500Ser) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128840110T>G | CA369225736 | FLNC | c.1499T>G (p.Phe500Cys) | |
| 7 | g.128840111T>A | CA369225738 | FLNC | c.1500T>A (p.Phe500Leu) | |
| 7 | g.128840111T>C | CA457582705 | FLNC | c.1500T>C (p.Phe500=) | |
| 7 | g.128840111T>G | CA369225739 | FLNC | c.1500T>G (p.Phe500Leu) | |
| 7 | g.128840112A>C | CA369225740 | FLNC | c.1501A>C (p.Thr501Pro) | |
| 7 | g.128840112A>G | CA369225741 | FLNC | c.1501A>G (p.Thr501Ala) | |
| 7 | g.128840112A>T | CA369225742 | FLNC | c.1501A>T (p.Thr501Ser) | |
| 7 | g.128840113C>A | CA369225743 | FLNC | c.1502C>A (p.Thr501Asn) | |
| 7 | g.128840113C= | CA1742545926 | FLNC | c.1502C= (p.Thr501=) | |
| 7 | g.128840113C>G | CA369225744 | FLNC | c.1502C>G (p.Thr501Ser) | |
| 7 | g.128840113C>T | CA248062 | FLNC | c.1502C>T (p.Thr501Ile) | ClinVar dbSNP |
| 7 | g.128840114del | CA2740097543 | FLNC | c.1503del (p.Lys502ArgfsTer22) | ClinVar |
| 7 | g.128840114C>A | CA457582722 | FLNC | c.1503C>A (p.Thr501=) | |
| 7 | g.128840114C= | CA1742545927 | FLNC | c.1503C= (p.Thr501=) | |
| 7 | g.128840114C>G | CA457582723 | FLNC | c.1503C>G (p.Thr501=) | |
| 7 | g.128840114C>T | CA4474360 | FLNC | c.1503C>T (p.Thr501=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128840114_128840115dup | CA2573141703 | FLNC | c.1503_1504dup (p.Lys502ThrfsTer23) | ClinVar dbSNP |
| 7 | g.128840115A>C | CA369225747 | FLNC | c.1504A>C (p.Lys502Gln) | |
| 7 | g.128840115A>G | CA369225749 | FLNC | c.1504A>G (p.Lys502Glu) | |
| 7 | g.128840115A>T | CA369225750 | FLNC | c.1504A>T (p.Lys502Ter) | |
| 7 | g.128840116A= | CA1742545928 | FLNC | c.1505A= (p.Lys502=) | |
| 7 | g.128840116A>C | CA369225754 | FLNC | c.1505A>C (p.Lys502Thr) | |
| 7 | g.128840116A>G | CA369225752 | FLNC | c.1505A>G (p.Lys502Arg) | |
| 7 | g.128840116A>T | CA4474361 | FLNC | c.1505A>T (p.Lys502Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840117G>A | CA4474362 | FLNC | c.1506G>A (p.Lys502=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128840117G>C | CA369225759 | FLNC | c.1506G>C (p.Lys502Asn) | |
| 7 | g.128840117G= | CA1742545929 | FLNC | c.1506G= (p.Lys502=) | |
| 7 | g.128840117G>T | CA369225758 | FLNC | c.1506G>T (p.Lys502Asn) | |
| 7 | g.128840118G>A | CA166216155 | FLNC | c.1507G>A (p.Gly503Ser) | dbSNP gnomAD v4 |
| 7 | g.128840118G>C | CA369225761 | FLNC | c.1507G>C (p.Gly503Arg) | |
| 7 | g.128840118G= | CA1742545930 | FLNC | c.1507G= (p.Gly503=) | |
| 7 | g.128840118G>T | CA369225763 | FLNC | c.1507G>T (p.Gly503Cys) | |
| 7 | g.128840119G>A | CA369225766 | FLNC | c.1508G>A (p.Gly503Asp) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128840119G>C | CA369225768 | FLNC | c.1508G>C (p.Gly503Ala) | |
| 7 | g.128840119G= | CA1742545931 | FLNC | c.1508G= (p.Gly503=) | |
| 7 | g.128840119G>T | CA369225769 | FLNC | c.1508G>T (p.Gly503Val) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128840120T>A | CA457582739 | FLNC | c.1509T>A (p.Gly503=) | |
| 7 | g.128840120T>C | CA457582741 | FLNC | c.1509T>C (p.Gly503=) | |
| 7 | g.128840120T>G | CA457582744 | FLNC | c.1509T>G (p.Gly503=) | |
| 7 | g.128840121G>A | CA369225770 | FLNC | c.1510G>A (p.Ala504Thr) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128840121G>C | CA369225772 | FLNC | c.1510G>C (p.Ala504Pro) | |
| 7 | g.128840121G= | CA1742545932 | FLNC | c.1510G= (p.Ala504=) | |
| 7 | g.128840121G>T | CA369225774 | FLNC | c.1510G>T (p.Ala504Ser) | |
| 7 | g.128840123_128840136del | CA2695208476 | FLNC | c.1512_1525del (p.Gly505GlnfsTer?) | |
| 7 | g.128840122C>A | CA369225776 | FLNC | c.1511C>A (p.Ala504Asp) | |
| 7 | g.128840122C= | CA1742545933 | FLNC | c.1511C= (p.Ala504=) | |
| 7 | g.128840122C>G | CA369225779 | FLNC | c.1511C>G (p.Ala504Gly) | |
| 7 | g.128840122C>T | CA369225780 | FLNC | c.1511C>T (p.Ala504Val) | |
| 7 | g.128840123C>A | CA457582760 | FLNC | c.1512C>A (p.Ala504=) | |
| 7 | g.128840123C= | CA1742545934 | FLNC | c.1512C= (p.Ala504=) | |
| 7 | g.128840123C>G | CA457582757 | FLNC | c.1512C>G (p.Ala504=) | |
| 7 | g.128840123C>T | CA4474364 | FLNC | c.1512C>T (p.Ala504=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840126_128840131dup | CA4474363 | FLNC | c.1515_1520dup (p.Gly507_Glu508insSerGly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128840124G>A | CA4474365 | FLNC | c.1513G>A (p.Gly505Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128840124G>C | CA369225785 | FLNC | c.1513G>C (p.Gly505Arg) | gnomAD v4 |
| 7 | g.128840124G= | CA1742545935 | FLNC | c.1513G= (p.Gly505=) | |
| 7 | g.128840124G>T | CA369225787 | FLNC | c.1513G>T (p.Gly505Cys) | |
| 7 | g.128840125G>A | CA4474366 | FLNC | c.1514G>A (p.Gly505Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128840125G>C | CA166216165 | FLNC | c.1514G>C (p.Gly505Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128840125G= | CA1742545936 | FLNC | c.1514G= (p.Gly505=) | |
| 7 | g.128840125G>T | CA369225789 | FLNC | c.1514G>T (p.Gly505Val) | |
| 7 | g.128840126C>A | CA457582773 | FLNC | c.1515C>A (p.Gly505=) | |
| 7 | g.128840126C= | CA1742545937 | FLNC | c.1515C= (p.Gly505=) | |
| 7 | g.128840126C>G | CA457582775 | FLNC | c.1515C>G (p.Gly505=) | |
| 7 | g.128840126C>T | CA457582777 | FLNC | c.1515C>T (p.Gly505=) | dbSNP |
| 7 | g.128840126_128840133delinsCAGCGGGG | CA1742545938 | FLNC | c.1515_1522delinsCAGCGGGG (p.Gly505=) | |
| 7 | g.128840127A>C | CA369225791 | FLNC | c.1516A>C (p.Ser506Arg) | |
| 7 | g.128840127A>G | CA369225793 | FLNC | c.1516A>G (p.Ser506Gly) | |
| 7 | g.128840127A>T | CA369225794 | FLNC | c.1516A>T (p.Ser506Cys) | |
| 7 | g.128840130_128840136del | CA658657716 | FLNC | c.1519_1525del (p.Gly507SerfsTer15) | ClinVar dbSNP |
| 7 | g.128840128G>A | CA369225796 | FLNC | c.1517G>A (p.Ser506Asn) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128840128G>C | CA369225798 | FLNC | c.1517G>C (p.Ser506Thr) | |
| 7 | g.128840128G= | CA1742545939 | FLNC | c.1517G= (p.Ser506=) | |
| 7 | g.128840128G>T | CA369225799 | FLNC | c.1517G>T (p.Ser506Ile) | gnomAD v4 |
| 7 | g.128840129C>A | CA369225803 | FLNC | c.1518C>A (p.Ser506Arg) | |
| 7 | g.128840129C= | CA1742545940 | FLNC | c.1518C= (p.Ser506=) | |
| 7 | g.128840129C>G | CA369225801 | FLNC | c.1518C>G (p.Ser506Arg) | |
| 7 | g.128840129C>T | CA4474367 | FLNC | c.1518C>T (p.Ser506=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |