Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128840123_128840136del | CA2695208476 | FLNC | c.1512_1525del (p.Gly505GlnfsTer?) | |
7 | g.128840130_128840136del | CA658657716 | FLNC | c.1519_1525del (p.Gly507SerfsTer15) | ClinVar dbSNP |
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) | ClinVar 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) | ClinVar |
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) | |
7 | g.128840142G>A | CA369225853 | FLNC | c.1531G>A (p.Val511Ile) | gnomAD v4 |
7 | g.128840142G>C | CA369225852 | FLNC | c.1531G>C (p.Val511Leu) | |
7 | g.128840142G>T | CA369225851 | FLNC | c.1531G>T (p.Val511Phe) | |
7 | g.128840143T>A | CA369225855 | FLNC | c.1532T>A (p.Val511Asp) | |
7 | g.128840143T>C | CA369225859 | FLNC | c.1532T>C (p.Val511Ala) | |
7 | g.128840143T>G | CA369225857 | FLNC | c.1532T>G (p.Val511Gly) | |
7 | g.128840144C>A | CA457582853 | FLNC | c.1533C>A (p.Val511=) | |
7 | g.128840144C>G | CA457582855 | FLNC | c.1533C>G (p.Val511=) | |
7 | g.128840144C>T | CA457582857 | FLNC | c.1533C>T (p.Val511=) | ClinVar dbSNP gnomAD v4 |
7 | g.128840145A>C | CA369225860 | FLNC | c.1534A>C (p.Thr512Pro) | |
7 | g.128840145A>G | CA369225862 | FLNC | c.1534A>G (p.Thr512Ala) | |
7 | g.128840145A>T | CA369225864 | FLNC | c.1534A>T (p.Thr512Ser) | |
7 | g.128840146C>A | CA369225867 | FLNC | c.1535C>A (p.Thr512Lys) | ClinVar dbSNP gnomAD v4 |
7 | g.128840146C= | CA1742545947 | FLNC | c.1535C= (p.Thr512=) | |
7 | g.128840146C>G | CA369225869 | FLNC | c.1535C>G (p.Thr512Arg) | |
7 | g.128840146C>T | CA4474371 | FLNC | c.1535C>T (p.Thr512Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128840147G>A | CA457582874 | FLNC | c.1536G>A (p.Thr512=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128840147G>C | CA457582876 | FLNC | c.1536G>C (p.Thr512=) | ClinVar dbSNP COSMIC |
7 | g.128840147G= | CA1742545948 | FLNC | c.1536G= (p.Thr512=) | |
7 | g.128840147G>T | CA457582878 | FLNC | c.1536G>T (p.Thr512=) | gnomAD v4 |
7 | g.128840148G>A | CA369225872 | FLNC | c.1537G>A (p.Val513Ile) | |
7 | g.128840148G>C | CA369225871 | FLNC | c.1537G>C (p.Val513Leu) | |
7 | g.128840148G>T | CA369225870 | FLNC | c.1537G>T (p.Val513Phe) | |
7 | g.128840149T>A | CA369225873 | FLNC | c.1538T>A (p.Val513Asp) | |
7 | g.128840149T>C | CA369225874 | FLNC | c.1538T>C (p.Val513Ala) | |
7 | g.128840149T>G | CA369225875 | FLNC | c.1538T>G (p.Val513Gly) |