| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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 | |
| 7 | g.128851486C>A | CA457849134 | FLNC,FLNC-AS1 | c.5700C>A (p.Ser1900=) c.5601C>A (p.Ser1867=) n.230G>T | |
| 7 | g.128851486C>G | CA457849136 | FLNC,FLNC-AS1 | c.5700C>G (p.Ser1900=) c.5601C>G (p.Ser1867=) n.230G>C | |
| 7 | g.128851486C>T | CA457849135 | FLNC,FLNC-AS1 | c.5700C>T (p.Ser1900=) c.5601C>T (p.Ser1867=) n.230G>A | |
| 7 | g.128851486_128851487insTGT | CA2580076613 | FLNC,FLNC-AS1 | c.5700_5701insTGT (p.Ser1900_Lys1901insCys) c.5601_5602insTGT (p.Ser1867_Lys1868insCys) n.229_230insACA | ClinVar |
| 7 | g.128851487A>C | CA369208062 | FLNC,FLNC-AS1 | c.5701A>C (p.Lys1901Gln) c.5602A>C (p.Lys1868Gln) n.229T>G | |
| 7 | g.128851487A>G | CA369208060 | FLNC,FLNC-AS1 | c.5701A>G (p.Lys1901Glu) c.5602A>G (p.Lys1868Glu) n.229T>C | |
| 7 | g.128851487A>T | CA369208058 | FLNC,FLNC-AS1 | c.5701A>T (p.Lys1901Ter) c.5602A>T (p.Lys1868Ter) n.229T>A | |
| 7 | g.128851488A>C | CA369208064 | FLNC,FLNC-AS1 | c.5702A>C (p.Lys1901Thr) c.5603A>C (p.Lys1868Thr) n.228T>G | COSMIC |
| 7 | g.128851488A>G | CA369208067 | FLNC,FLNC-AS1 | c.5702A>G (p.Lys1901Arg) c.5603A>G (p.Lys1868Arg) n.228T>C | |
| 7 | g.128851488A>T | CA369208066 | FLNC,FLNC-AS1 | c.5702A>T (p.Lys1901Met) c.5603A>T (p.Lys1868Met) n.228T>A | |
| 7 | g.128851488_128851489delinsAG | CA1742571110 | FLNC,FLNC-AS1 | c.5702_5703delinsAG (p.Lys1901=) c.5603_5604delinsAG (p.Lys1868=) n.227_228delinsCT | |
| 7 | g.128851489G>A | CA457849140 | FLNC,FLNC-AS1 | c.5703G>A (p.Lys1901=) c.5604G>A (p.Lys1868=) n.227C>T | ClinVar dbSNP gnomAD v4 |
| 7 | g.128851489G>C | CA369208069 | FLNC,FLNC-AS1 | c.5703G>C (p.Lys1901Asn) c.5604G>C (p.Lys1868Asn) n.227C>G | |
| 7 | g.128851489G= | CA1742571117 | FLNC,FLNC-AS1 | c.5703G= (p.Lys1901=) c.5604G= (p.Lys1868=) n.227C= | |
| 7 | g.128851489G>T | CA369208070 | FLNC,FLNC-AS1 | c.5703G>T (p.Lys1901Asn) c.5604G>T (p.Lys1868Asn) n.227C>A | |
| 7 | g.128851490del | CA645372844 | FLNC,FLNC-AS1 | c.5704del (p.Ala1902GlnfsTer?) c.5605del (p.Ala1869GlnfsTer?) n.227del | ClinVar dbSNP |
| 7 | g.128851490G>A | CA369208072 | FLNC,FLNC-AS1 | c.5704G>A (p.Ala1902Thr) c.5605G>A (p.Ala1869Thr) n.226C>T | |
| 7 | g.128851490G>C | CA369208075 | FLNC,FLNC-AS1 | c.5704G>C (p.Ala1902Pro) c.5605G>C (p.Ala1869Pro) n.226C>G | |
| 7 | g.128851490G>T | CA369208074 | FLNC,FLNC-AS1 | c.5704G>T (p.Ala1902Ser) c.5605G>T (p.Ala1869Ser) n.226C>A | |
| 7 | g.128851491C>A | CA369208078 | FLNC,FLNC-AS1 | c.5705C>A (p.Ala1902Glu) c.5606C>A (p.Ala1869Glu) n.225G>T | ClinVar |