Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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) | |
7 | g.128840150C>A | CA457582896 | FLNC | c.1539C>A (p.Val513=) | |
7 | g.128840150C>G | CA457582897 | FLNC | c.1539C>G (p.Val513=) | ClinVar dbSNP |
7 | g.128840150C>T | CA457582893 | FLNC | c.1539C>T (p.Val513=) | |
7 | g.128840151A>C | CA369225876 | FLNC | c.1540A>C (p.Lys514Gln) | |
7 | g.128840151A>G | CA369225877 | FLNC | c.1540A>G (p.Lys514Glu) | |
7 | g.128840151A>T | CA369225878 | FLNC | c.1540A>T (p.Lys514Ter) | |
7 | g.128840152A= | CA1742545949 | FLNC | c.1541A= (p.Lys514=) | |
7 | g.128840152A>C | CA4474372 | FLNC | c.1541A>C (p.Lys514Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128840152A>G | CA369225880 | FLNC | c.1541A>G (p.Lys514Arg) | ClinVar |
7 | g.128840152A>T | CA369225879 | FLNC | c.1541A>T (p.Lys514Met) | |
7 | g.128840153G>A | CA4474373 | FLNC | c.1542G>A (p.Lys514=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
7 | g.128840153G>C | CA369225881 | FLNC | c.1542G>C (p.Lys514Asn) | |
7 | g.128840153G= | CA1742545950 | FLNC | c.1542G= (p.Lys514=) | |
7 | g.128840153G>T | CA369225882 | FLNC | c.1542G>T (p.Lys514Asn) | COSMIC |
7 | g.128840154G>A | CA4474374 | FLNC | c.1543G>A (p.Gly515Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128840154G>C | CA369225883 | FLNC | c.1543G>C (p.Gly515Arg) | |
7 | g.128840154G= | CA1742545951 | FLNC | c.1543G= (p.Gly515=) |