Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128851472G>A | CA166188974 | FLNC,FLNC-AS1 | c.5686G>A (p.Val1896Met) c.5587G>A (p.Val1863Met) n.244C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.128851472G>C | CA369208003 | FLNC,FLNC-AS1 | c.5686G>C (p.Val1896Leu) c.5587G>C (p.Val1863Leu) n.244C>G | |
7 | g.128851472G= | CA1742571073 | FLNC,FLNC-AS1 | c.5686G= (p.Val1896=) c.5587G= (p.Val1863=) n.244C= | |
7 | g.128851472G>T | CA369208001 | FLNC,FLNC-AS1 | c.5686G>T (p.Val1896Leu) c.5587G>T (p.Val1863Leu) n.244C>A | |
7 | g.128851473T>A | CA369208006 | FLNC,FLNC-AS1 | c.5687T>A (p.Val1896Glu) c.5588T>A (p.Val1863Glu) n.243A>T | |
7 | g.128851473T>C | CA369208009 | FLNC,FLNC-AS1 | c.5687T>C (p.Val1896Ala) c.5588T>C (p.Val1863Ala) n.243A>G | |
7 | g.128851473T>G | CA369208007 | FLNC,FLNC-AS1 | c.5687T>G (p.Val1896Gly) c.5588T>G (p.Val1863Gly) n.243A>C | ClinVar |
7 | g.128851474G>A | CA457849118 | FLNC,FLNC-AS1 | c.5688G>A (p.Val1896=) c.5589G>A (p.Val1863=) n.242C>T | gnomAD v4 |
7 | g.128851474G>C | CA457849116 | FLNC,FLNC-AS1 | c.5688G>C (p.Val1896=) c.5589G>C (p.Val1863=) n.242C>G | |
7 | g.128851474G>T | CA457849117 | FLNC,FLNC-AS1 | c.5688G>T (p.Val1896=) c.5589G>T (p.Val1863=) n.242C>A | |
7 | g.128851475G>A | CA369208011 | FLNC,FLNC-AS1 | c.5689G>A (p.Glu1897Lys) c.5590G>A (p.Glu1864Lys) n.241C>T | |
7 | g.128851475G>C | CA369208013 | FLNC,FLNC-AS1 | c.5689G>C (p.Glu1897Gln) c.5590G>C (p.Glu1864Gln) n.241C>G | |
7 | g.128851475G>T | CA369208014 | FLNC,FLNC-AS1 | c.5689G>T (p.Glu1897Ter) c.5590G>T (p.Glu1864Ter) n.241C>A | |
7 | g.128851476A>C | CA369208017 | FLNC,FLNC-AS1 | c.5690A>C (p.Glu1897Ala) c.5591A>C (p.Glu1864Ala) n.240T>G | |
7 | g.128851476A>G | CA369208019 | FLNC,FLNC-AS1 | c.5690A>G (p.Glu1897Gly) c.5591A>G (p.Glu1864Gly) n.240T>C | ClinVar |
7 | g.128851476A>T | CA369208020 | FLNC,FLNC-AS1 | c.5690A>T (p.Glu1897Val) c.5591A>T (p.Glu1864Val) n.240T>A | COSMIC |
7 | g.128851477G>A | CA457849119 | FLNC,FLNC-AS1 | c.5691G>A (p.Glu1897=) c.5592G>A (p.Glu1864=) n.239C>T | |
7 | g.128851477G>C | CA369208022 | FLNC,FLNC-AS1 | c.5691G>C (p.Glu1897Asp) c.5592G>C (p.Glu1864Asp) n.239C>G | dbSNP |
7 | g.128851477G= | CA1742571084 | FLNC,FLNC-AS1 | c.5691G= (p.Glu1897=) c.5592G= (p.Glu1864=) n.239C= | |
7 | g.128851477G>T | CA369208024 | FLNC,FLNC-AS1 | c.5691G>T (p.Glu1897Asp) c.5592G>T (p.Glu1864Asp) n.239C>A | |
7 | g.128851479del | CA2580076611 | FLNC,FLNC-AS1 | c.5693del (p.Gly1898AlafsTer?) c.5594del (p.Gly1865AlafsTer?) n.239del | ClinVar gnomAD v4 |
7 | g.128851478G>A | CA369208026 | FLNC,FLNC-AS1 | c.5692G>A (p.Gly1898Ser) c.5593G>A (p.Gly1865Ser) n.238C>T | |
7 | g.128851478G>C | CA369208027 | FLNC,FLNC-AS1 | c.5692G>C (p.Gly1898Arg) c.5593G>C (p.Gly1865Arg) n.238C>G | |
7 | g.128851478G>T | CA369208029 | FLNC,FLNC-AS1 | c.5692G>T (p.Gly1898Cys) c.5593G>T (p.Gly1865Cys) n.238C>A | |
7 | g.128851479G>A | CA369208034 | FLNC,FLNC-AS1 | c.5693G>A (p.Gly1898Asp) c.5594G>A (p.Gly1865Asp) n.237C>T | ClinVar dbSNP |
7 | g.128851479G>C | CA369208032 | FLNC,FLNC-AS1 | c.5693G>C (p.Gly1898Ala) c.5594G>C (p.Gly1865Ala) n.237C>G | |
7 | g.128851479G= | CA1742571091 | FLNC,FLNC-AS1 | c.5693G= (p.Gly1898=) c.5594G= (p.Gly1865=) n.237C= | |
7 | g.128851479G>T | CA369208031 | FLNC,FLNC-AS1 | c.5693G>T (p.Gly1898Val) c.5594G>T (p.Gly1865Val) n.237C>A | |
7 | g.128851480C>A | CA457849125 | FLNC,FLNC-AS1 | c.5694C>A (p.Gly1898=) c.5595C>A (p.Gly1865=) n.236G>T | |
7 | g.128851480C>G | CA457849127 | FLNC,FLNC-AS1 | c.5694C>G (p.Gly1898=) c.5595C>G (p.Gly1865=) n.236G>C | |
7 | g.128851480C>T | CA457849126 | FLNC,FLNC-AS1 | c.5694C>T (p.Gly1898=) c.5595C>T (p.Gly1865=) n.236G>A | |
7 | g.128851481C>A | CA369208036 | FLNC,FLNC-AS1 | c.5695C>A (p.Pro1899Thr) c.5596C>A (p.Pro1866Thr) n.235G>T | |
7 | g.128851481C= | CA1742571097 | FLNC,FLNC-AS1 | c.5695C= (p.Pro1899=) c.5596C= (p.Pro1866=) n.235G= | |
7 | g.128851481C>G | CA369208037 | FLNC,FLNC-AS1 | c.5695C>G (p.Pro1899Ala) c.5596C>G (p.Pro1866Ala) n.235G>C | |
7 | g.128851481C>T | CA4475762 | FLNC,FLNC-AS1 | c.5695C>T (p.Pro1899Ser) c.5596C>T (p.Pro1866Ser) n.235G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128851482C>A | CA369208040 | FLNC,FLNC-AS1 | c.5696C>A (p.Pro1899Gln) c.5597C>A (p.Pro1866Gln) n.234G>T | |
7 | g.128851482C= | CA1742571101 | FLNC,FLNC-AS1 | c.5696C= (p.Pro1899=) c.5597C= (p.Pro1866=) n.234G= | |
7 | g.128851482C>G | CA369208042 | FLNC,FLNC-AS1 | c.5696C>G (p.Pro1899Arg) c.5597C>G (p.Pro1866Arg) n.234G>C | |
7 | g.128851482C>T | CA369208044 | FLNC,FLNC-AS1 | c.5696C>T (p.Pro1899Leu) c.5597C>T (p.Pro1866Leu) n.234G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.128851483A= | CA1742571105 | FLNC,FLNC-AS1 | c.5697A= (p.Pro1899=) c.5598A= (p.Pro1866=) n.233T= | |
7 | g.128851483A>C | CA457849130 | FLNC,FLNC-AS1 | c.5697A>C (p.Pro1899=) c.5598A>C (p.Pro1866=) n.233T>G | |
7 | g.128851483A>G | CA457849132 | FLNC,FLNC-AS1 | c.5697A>G (p.Pro1899=) c.5598A>G (p.Pro1866=) n.233T>C | ClinVar dbSNP |
7 | g.128851483A>T | CA457849133 | FLNC,FLNC-AS1 | c.5697A>T (p.Pro1899=) c.5598A>T (p.Pro1866=) n.233T>A | |
7 | g.128851483dup | CA658797015 | FLNC,FLNC-AS1 | c.5697dup (p.Ser1900IlefsTer8) c.5598dup (p.Ser1867IlefsTer8) n.233dup | ClinVar dbSNP |
7 | g.128851484T>A | CA369208046 | FLNC,FLNC-AS1 | c.5698T>A (p.Ser1900Thr) c.5599T>A (p.Ser1867Thr) n.232A>T | |
7 | g.128851484T>C | CA369208048 | FLNC,FLNC-AS1 | c.5698T>C (p.Ser1900Pro) c.5599T>C (p.Ser1867Pro) n.232A>G | ClinVar |
7 | g.128851484T>G | CA369208050 | FLNC,FLNC-AS1 | c.5698T>G (p.Ser1900Ala) c.5599T>G (p.Ser1867Ala) n.232A>C | |
7 | g.128851485C>A | CA369208052 | FLNC,FLNC-AS1 | c.5699C>A (p.Ser1900Tyr) c.5600C>A (p.Ser1867Tyr) n.231G>T | |
7 | g.128851485C>G | CA369208054 | FLNC,FLNC-AS1 | c.5699C>G (p.Ser1900Cys) c.5600C>G (p.Ser1867Cys) n.231G>C | gnomAD v4 |
7 | g.128851485C>T | CA369208056 | FLNC,FLNC-AS1 | c.5699C>T (p.Ser1900Phe) c.5600C>T (p.Ser1867Phe) n.231G>A |