| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128849443_128849463dup | CA1742564518 | FLNC | c.5064_5084dup (p.Val1695_Glu1696insGluLeuAspValAspValVal) | ClinVar dbSNP |
| 7 | g.128849461G>A | CA457848925 | FLNC | c.5082G>A (p.Val1694=) | |
| 7 | g.128849461G>C | CA457848926 | FLNC | c.5082G>C (p.Val1694=) | |
| 7 | g.128849461G>T | CA457848927 | FLNC | c.5082G>T (p.Val1694=) | |
| 7 | g.128849462G>A | CA369204137 | FLNC | c.5083G>A (p.Val1695Ile) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128849462G>C | CA369204138 | FLNC | c.5083G>C (p.Val1695Leu) | |
| 7 | g.128849462G= | CA1742564597 | FLNC | c.5083G= (p.Val1695=) | |
| 7 | g.128849462G>T | CA369204139 | FLNC | c.5083G>T (p.Val1695Phe) | |
| 7 | g.128849463T>A | CA369204140 | FLNC | c.5084T>A (p.Val1695Asp) | |
| 7 | g.128849463T>C | CA4475555 | FLNC | c.5084T>C (p.Val1695Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128849463T>G | CA369204141 | FLNC | c.5084T>G (p.Val1695Gly) | |
| 7 | g.128849463T= | CA1742564606 | FLNC | c.5084T= (p.Val1695=) | |
| 7 | g.128849464T>A | CA457848931 | FLNC | c.5085T>A (p.Val1695=) | |
| 7 | g.128849464T>C | CA457848933 | FLNC | c.5085T>C (p.Val1695=) | |
| 7 | g.128849464T>G | CA457848934 | FLNC | c.5085T>G (p.Val1695=) | |
| 7 | g.128849465G>A | CA369204142 | FLNC | c.5086G>A (p.Glu1696Lys) | |
| 7 | g.128849465G>C | CA369204144 | FLNC | c.5086G>C (p.Glu1696Gln) | COSMIC |
| 7 | g.128849465G>T | CA369204143 | FLNC | c.5086G>T (p.Glu1696Ter) | |
| 7 | g.128849466A>C | CA369204145 | FLNC | c.5087A>C (p.Glu1696Ala) | |
| 7 | g.128849466A>G | CA369204146 | FLNC | c.5087A>G (p.Glu1696Gly) | |
| 7 | g.128849466A>T | CA369204147 | FLNC | c.5087A>T (p.Glu1696Val) | |
| 7 | g.128849467G>A | CA457848936 | FLNC | c.5088G>A (p.Glu1696=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128849467G>C | CA369204148 | FLNC | c.5088G>C (p.Glu1696Asp) | ClinVar dbSNP |
| 7 | g.128849467G= | CA1742564623 | FLNC | c.5088G= (p.Glu1696=) | |
| 7 | g.128849467G>T | CA369204149 | FLNC | c.5088G>T (p.Glu1696Asp) | |
| 7 | g.128849468A>C | CA369204150 | FLNC | c.5089A>C (p.Asn1697His) | |
| 7 | g.128849468A>G | CA369204151 | FLNC | c.5089A>G (p.Asn1697Asp) | |
| 7 | g.128849468A>T | CA369204152 | FLNC | c.5089A>T (p.Asn1697Tyr) | |
| 7 | g.128849469A>C | CA369204153 | FLNC | c.5090A>C (p.Asn1697Thr) | |
| 7 | g.128849469A>G | CA369204154 | FLNC | c.5090A>G (p.Asn1697Ser) | |
| 7 | g.128849469A>T | CA369204155 | FLNC | c.5090A>T (p.Asn1697Ile) | |
| 7 | g.128849470C>A | CA369204156 | FLNC | c.5091C>A (p.Asn1697Lys) | |
| 7 | g.128849470C>G | CA369204157 | FLNC | c.5091C>G (p.Asn1697Lys) | |
| 7 | g.128849470C>T | CA457848942 | FLNC | c.5091C>T (p.Asn1697=) | |
| 7 | g.128849471C>A | CA369204160 | FLNC | c.5092C>A (p.His1698Asn) | |
| 7 | g.128849471C>G | CA369204159 | FLNC | c.5092C>G (p.His1698Asp) | gnomAD v4 |
| 7 | g.128849471C>T | CA369204158 | FLNC | c.5092C>T (p.His1698Tyr) | |
| 7 | g.128849472A>C | CA369204161 | FLNC | c.5093A>C (p.His1698Pro) | |
| 7 | g.128849472A>G | CA369204162 | FLNC | c.5093A>G (p.His1698Arg) | COSMIC |
| 7 | g.128849472A>T | CA369204163 | FLNC | c.5093A>T (p.His1698Leu) | |
| 7 | g.128849473T>A | CA369204164 | FLNC | c.5094T>A (p.His1698Gln) | |
| 7 | g.128849473T>C | CA457848948 | FLNC | c.5094T>C (p.His1698=) | dbSNP gnomAD v4 |
| 7 | g.128849473T>G | CA369204165 | FLNC | c.5094T>G (p.His1698Gln) | |
| 7 | g.128849473T= | CA1742564636 | FLNC | c.5094T= (p.His1698=) | |
| 7 | g.128849474G>A | CA369204166 | FLNC | c.5095G>A (p.Asp1699Asn) | |
| 7 | g.128849474G>C | CA369204167 | FLNC | c.5095G>C (p.Asp1699His) | |
| 7 | g.128849474G>T | CA369204168 | FLNC | c.5095G>T (p.Asp1699Tyr) | |
| 7 | g.128849475A>C | CA369204169 | FLNC | c.5096A>C (p.Asp1699Ala) | |
| 7 | g.128849475A>G | CA369204170 | FLNC | c.5096A>G (p.Asp1699Gly) | |
| 7 | g.128849475A>T | CA369204171 | FLNC | c.5096A>T (p.Asp1699Val) |