| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128849349G>A | CA4475534 | FLNC | c.4970G>A (p.Arg1657Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128849349G>C | CA369203898 | FLNC | c.4970G>C (p.Arg1657Pro) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128849349G= | CA1742564137 | FLNC | c.4970G= (p.Arg1657=) | |
| 7 | g.128849349G>T | CA369203899 | FLNC | c.4970G>T (p.Arg1657Leu) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128849350A= | CA1742564141 | FLNC | c.4971A= (p.Arg1657=) | |
| 7 | g.128849350A>C | CA457848964 | FLNC | c.4971A>C (p.Arg1657=) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128849350A>G | CA457848965 | FLNC | c.4971A>G (p.Arg1657=) | dbSNP |
| 7 | g.128849350A>T | CA457848967 | FLNC | c.4971A>T (p.Arg1657=) | |
| 7 | g.128849351A>C | CA369203900 | FLNC | c.4972A>C (p.Ile1658Leu) | |
| 7 | g.128849351A>G | CA369203901 | FLNC | c.4972A>G (p.Ile1658Val) | |
| 7 | g.128849351A>T | CA369203902 | FLNC | c.4972A>T (p.Ile1658Phe) | |
| 7 | g.128849352T>A | CA369203904 | FLNC | c.4973T>A (p.Ile1658Asn) | |
| 7 | g.128849352T>C | CA369203905 | FLNC | c.4973T>C (p.Ile1658Thr) | |
| 7 | g.128849352T>G | CA369203903 | FLNC | c.4973T>G (p.Ile1658Ser) | |
| 7 | g.128849353C>A | CA457848969 | FLNC | c.4974C>A (p.Ile1658=) | gnomAD v4 |
| 7 | g.128849353C>G | CA369203906 | FLNC | c.4974C>G (p.Ile1658Met) | |
| 7 | g.128849353C>T | CA457848970 | FLNC | c.4974C>T (p.Ile1658=) | gnomAD v4 |
| 7 | g.128849354C>A | CA369203907 | FLNC | c.4975C>A (p.Gln1659Lys) | |
| 7 | g.128849354C>G | CA369203908 | FLNC | c.4975C>G (p.Gln1659Glu) | |
| 7 | g.128849354C>T | CA369203909 | FLNC | c.4975C>T (p.Gln1659Ter) | |
| 7 | g.128849355A>C | CA369203910 | FLNC | c.4976A>C (p.Gln1659Pro) | |
| 7 | g.128849355A>G | CA369203911 | FLNC | c.4976A>G (p.Gln1659Arg) | |
| 7 | g.128849355A>T | CA369203912 | FLNC | c.4976A>T (p.Gln1659Leu) | |
| 7 | g.128849356G>A | CA457848978 | FLNC | c.4977G>A (p.Gln1659=) | |
| 7 | g.128849356G>C | CA369203913 | FLNC | c.4977G>C (p.Gln1659His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128849356G= | CA1742564150 | FLNC | c.4977G= (p.Gln1659=) | |
| 7 | g.128849356G>T | CA369203914 | FLNC | c.4977G>T (p.Gln1659His) | |
| 7 | g.128849357A>C | CA369203915 | FLNC | c.4978A>C (p.Ile1660Leu) | |
| 7 | g.128849357A>G | CA369203916 | FLNC | c.4978A>G (p.Ile1660Val) | |
| 7 | g.128849357A>T | CA369203917 | FLNC | c.4978A>T (p.Ile1660Phe) | |
| 7 | g.128849358T>A | CA369203918 | FLNC | c.4979T>A (p.Ile1660Asn) | |
| 7 | g.128849358T>C | CA4475535 | FLNC | c.4979T>C (p.Ile1660Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128849358T>G | CA369203919 | FLNC | c.4979T>G (p.Ile1660Ser) | |
| 7 | g.128849358T= | CA1742564155 | FLNC | c.4979T= (p.Ile1660=) | |
| 7 | g.128849359T>A | CA457848982 | FLNC | c.4980T>A (p.Ile1660=) | |
| 7 | g.128849359T>C | CA457848983 | FLNC | c.4980T>C (p.Ile1660=) | |
| 7 | g.128849359T>G | CA369203920 | FLNC | c.4980T>G (p.Ile1660Met) | |
| 7 | g.128849360G>A | CA369203921 | FLNC | c.4981G>A (p.Gly1661Arg) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128849360G>C | CA369203922 | FLNC | c.4981G>C (p.Gly1661Arg) | |
| 7 | g.128849360G>T | CA369203923 | FLNC | c.4981G>T (p.Gly1661Trp) | |
| 7 | g.128849361G>A | CA369203924 | FLNC | c.4982G>A (p.Gly1661Glu) | |
| 7 | g.128849361G>C | CA369203925 | FLNC | c.4982G>C (p.Gly1661Ala) | gnomAD v4 |
| 7 | g.128849361G>T | CA369203926 | FLNC | c.4982G>T (p.Gly1661Val) | COSMIC |
| 7 | g.128849362G>A | CA166185347 | FLNC | c.4983G>A (p.Gly1661=) | dbSNP |
| 7 | g.128849362G>C | CA457848990 | FLNC | c.4983G>C (p.Gly1661=) | |
| 7 | g.128849362G= | CA1742564160 | FLNC | c.4983G= (p.Gly1661=) | |
| 7 | g.128849362G>T | CA457848993 | FLNC | c.4983G>T (p.Gly1661=) | |
| 7 | g.128849363C>A | CA369203927 | FLNC | c.4984C>A (p.Gln1662Lys) | |
| 7 | g.128849363C= | CA1742564164 | FLNC | c.4984C= (p.Gln1662=) | |
| 7 | g.128849363C>G | CA369203928 | FLNC | c.4984C>G (p.Gln1662Glu) |