Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 |