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