Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128840123_128840136del | CA2695208476 | FLNC | c.1512_1525del (p.Gly505GlnfsTer?) | |
7 | g.128840126_128840131dup | CA4474363 | FLNC | c.1515_1520dup (p.Gly507_Glu508insSerGly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128840126_128840133delinsCAGCGGGG | CA1742545938 | FLNC | c.1515_1522delinsCAGCGGGG (p.Gly505=) | |
7 | g.128840130_128840136del | CA658657716 | FLNC | c.1519_1525del (p.Gly507SerfsTer15) | ClinVar dbSNP |
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 |
7 | g.128840130G>A | CA4474368 | FLNC | c.1519G>A (p.Gly507Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128840130G>C | CA369225804 | FLNC | c.1519G>C (p.Gly507Arg) | |
7 | g.128840130G= | CA1742545941 | FLNC | c.1519G= (p.Gly507=) | |
7 | g.128840130G>T | CA369225805 | FLNC | c.1519G>T (p.Gly507Trp) | |
7 | g.128840131G>A | CA369225806 | FLNC | c.1520G>A (p.Gly507Glu) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128840131G>C | CA369225808 | FLNC | c.1520G>C (p.Gly507Ala) | |
7 | g.128840131G= | CA1742545942 | FLNC | c.1520G= (p.Gly507=) | |
7 | g.128840131G>T | CA369225810 | FLNC | c.1520G>T (p.Gly507Val) | |
7 | g.128840132G>A | CA457582796 | FLNC | c.1521G>A (p.Gly507=) | dbSNP |
7 | g.128840132G>C | CA457582798 | FLNC | c.1521G>C (p.Gly507=) | |
7 | g.128840132G>T | CA457582800 | FLNC | c.1521G>T (p.Gly507=) | |
7 | g.128840133G>A | CA369225813 | FLNC | c.1522G>A (p.Glu508Lys) | |
7 | g.128840133G>C | CA369225815 | FLNC | c.1522G>C (p.Glu508Gln) | COSMIC |
7 | g.128840133G>T | CA369225817 | FLNC | c.1522G>T (p.Glu508Ter) | |
7 | g.128840134A>C | CA369225819 | FLNC | c.1523A>C (p.Glu508Ala) | ClinVar |
7 | g.128840134A>G | CA369225821 | FLNC | c.1523A>G (p.Glu508Gly) | |
7 | g.128840134A>T | CA369225823 | FLNC | c.1523A>T (p.Glu508Val) | |
7 | g.128840135G>A | CA457582818 | FLNC | c.1524G>A (p.Glu508=) | |
7 | g.128840135G>C | CA369225824 | FLNC | c.1524G>C (p.Glu508Asp) | |
7 | g.128840135G>T | CA369225825 | FLNC | c.1524G>T (p.Glu508Asp) | |
7 | g.128840136C>A | CA369225831 | FLNC | c.1525C>A (p.Leu509Ile) | |
7 | g.128840136C>G | CA369225827 | FLNC | c.1525C>G (p.Leu509Val) | ClinVar |
7 | g.128840136C>T | CA369225829 | FLNC | c.1525C>T (p.Leu509Phe) | gnomAD v4 |
7 | g.128840137T>A | CA369225833 | FLNC | c.1526T>A (p.Leu509His) | |
7 | g.128840137T>C | CA4474369 | FLNC | c.1526T>C (p.Leu509Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128840137T>G | CA369225835 | FLNC | c.1526T>G (p.Leu509Arg) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128840137T= | CA1742545943 | FLNC | c.1526T= (p.Leu509=) | |
7 | g.128840138C>A | CA457582828 | FLNC | c.1527C>A (p.Leu509=) | |
7 | g.128840138C= | CA1742545944 | FLNC | c.1527C= (p.Leu509=) | |
7 | g.128840138C>G | CA457582831 | FLNC | c.1527C>G (p.Leu509=) | COSMIC |
7 | g.128840138C>T | CA4474370 | FLNC | c.1527C>T (p.Leu509=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128840139A= | CA1742545945 | FLNC | c.1528A= (p.Lys510=) | |
7 | g.128840139A>C | CA16618350 | FLNC | c.1528A>C (p.Lys510Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128840139A>G | CA369225839 | FLNC | c.1528A>G (p.Lys510Glu) | gnomAD v4 |
7 | g.128840139A>T | CA369225840 | FLNC | c.1528A>T (p.Lys510Ter) | |
7 | g.128840140A= | CA1742545946 | FLNC | c.1529A= (p.Lys510=) | |
7 | g.128840140A>C | CA369225842 | FLNC | c.1529A>C (p.Lys510Thr) | |
7 | g.128840140A>G | CA369225843 | FLNC | c.1529A>G (p.Lys510Arg) | dbSNP |
7 | g.128840140A>T | CA369225845 | FLNC | c.1529A>T (p.Lys510Met) | |
7 | g.128840141G>A | CA457582837 | FLNC | c.1530G>A (p.Lys510=) | ClinVar |
7 | g.128840141G>C | CA369225847 | FLNC | c.1530G>C (p.Lys510Asn) | |
7 | g.128840141G>T | CA369225848 | FLNC | c.1530G>T (p.Lys510Asn) |