Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128847784_128847841del | CA2573049001 | FLNC | c.4376_4433del (p.Ala1459GlyfsTer?) | |
7 | g.128847829_128847858del | CA2684813848 | FLNC | c.4421_4450del (p.Arg1474_Gly1483del) | gnomAD v4 |
7 | g.128847827_128847841del | CA2573049012 | FLNC | c.4419_4433del (p.Arg1474_Gln1478del) | |
7 | g.128847839G>A | CA152862 | FLNC | c.4431G>A (p.Leu1477=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128847839G>C | CA457848641 | FLNC | c.4431G>C (p.Leu1477=) | |
7 | g.128847839G= | CA1742589384 | FLNC | c.4431G= (p.Leu1477=) | |
7 | g.128847839G>T | CA457848642 | FLNC | c.4431G>T (p.Leu1477=) | |
7 | g.128847839_128847840insGTGGCTGTGCTGGGCCCCACAGGTATAGAATGGCCGGGGGCCCCTA | CA2715891717 | FLNC | c.4431_4432insGTGGCTGTGCTGGGCCCCACAGGTATAGAATGGCCGGGGGCCCCTA (p.Gln1478ValfsTer?) | dbSNP |
7 | g.128847840C>A | CA369201618 | FLNC | c.4432C>A (p.Gln1478Lys) | |
7 | g.128847840C>G | CA369201619 | FLNC | c.4432C>G (p.Gln1478Glu) | |
7 | g.128847840C>T | CA369201621 | FLNC | c.4432C>T (p.Gln1478Ter) | ClinVar dbSNP |
7 | g.128847841A>C | CA369201623 | FLNC | c.4433A>C (p.Gln1478Pro) | |
7 | g.128847841A>G | CA369201625 | FLNC | c.4433A>G (p.Gln1478Arg) | COSMIC |
7 | g.128847841A>T | CA369201627 | FLNC | c.4433A>T (p.Gln1478Leu) | |
7 | g.128847842G>A | CA457848646 | FLNC | c.4434G>A (p.Gln1478=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.128847842G>C | CA369201630 | FLNC | c.4434G>C (p.Gln1478His) | |
7 | g.128847842G= | CA1742589385 | FLNC | c.4434G= (p.Gln1478=) | |
7 | g.128847842G>T | CA369201629 | FLNC | c.4434G>T (p.Gln1478His) | |
7 | g.128847843G>A | CA369201633 | FLNC | c.4435G>A (p.Val1479Met) | |
7 | g.128847843G>C | CA369201635 | FLNC | c.4435G>C (p.Val1479Leu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.128847843G= | CA1742589386 | FLNC | c.4435G= (p.Val1479=) | |
7 | g.128847843G>T | CA369201637 | FLNC | c.4435G>T (p.Val1479Leu) | dbSNP |
7 | g.128847844T>A | CA369201639 | FLNC | c.4436T>A (p.Val1479Glu) | |
7 | g.128847844T>C | CA369201641 | FLNC | c.4436T>C (p.Val1479Ala) | |
7 | g.128847844T>G | CA369201643 | FLNC | c.4436T>G (p.Val1479Gly) | dbSNP |
7 | g.128847845G>A | CA457848654 | FLNC | c.4437G>A (p.Val1479=) | |
7 | g.128847845G>C | CA457848655 | FLNC | c.4437G>C (p.Val1479=) | COSMIC |
7 | g.128847845G>T | CA457848657 | FLNC | c.4437G>T (p.Val1479=) | |
7 | g.128847846G>A | CA369201645 | FLNC | c.4438G>A (p.Ala1480Thr) | |
7 | g.128847846G>C | CA369201647 | FLNC | c.4438G>C (p.Ala1480Pro) | |
7 | g.128847846G>T | CA369201649 | FLNC | c.4438G>T (p.Ala1480Ser) | gnomAD v4 |
7 | g.128847847C>A | CA369201651 | FLNC | c.4439C>A (p.Ala1480Asp) | gnomAD v4 |
7 | g.128847847C>G | CA369201653 | FLNC | c.4439C>G (p.Ala1480Gly) | |
7 | g.128847847C>T | CA369201655 | FLNC | c.4439C>T (p.Ala1480Val) | |
7 | g.128847847_128847853del | CA2573049002 | FLNC | c.4439_4445del (p.Ala1480GlyfsTer?) | |
7 | g.128847848T>A | CA457848661 | FLNC | c.4440T>A (p.Ala1480=) | |
7 | g.128847848T>C | CA457848662 | FLNC | c.4440T>C (p.Ala1480=) | |
7 | g.128847848T>G | CA457848663 | FLNC | c.4440T>G (p.Ala1480=) | |
7 | g.128847849G>A | CA369201659 | FLNC | c.4441G>A (p.Val1481Met) | ClinVar |
7 | g.128847849G>C | CA369201661 | FLNC | c.4441G>C (p.Val1481Leu) | |
7 | g.128847849G>T | CA369201657 | FLNC | c.4441G>T (p.Val1481Leu) | gnomAD v4 |
7 | g.128847850T>A | CA369201663 | FLNC | c.4442T>A (p.Val1481Glu) | |
7 | g.128847850T>C | CA369201665 | FLNC | c.4442T>C (p.Val1481Ala) | |
7 | g.128847850T>G | CA369201667 | FLNC | c.4442T>G (p.Val1481Gly) | dbSNP |
7 | g.128847850T= | CA1742589387 | FLNC | c.4442T= (p.Val1481=) | |
7 | g.128847851G>A | CA457848665 | FLNC | c.4443G>A (p.Val1481=) | |
7 | g.128847851G>C | CA457848666 | FLNC | c.4443G>C (p.Val1481=) | |
7 | g.128847851G>T | CA457848667 | FLNC | c.4443G>T (p.Val1481=) | |
7 | g.128847852C>A | CA369201669 | FLNC | c.4444C>A (p.Leu1482Met) | |
7 | g.128847852C>G | CA369201670 | FLNC | c.4444C>G (p.Leu1482Val) |