| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128849379C>A | CA369203963 | FLNC | c.5000C>A (p.Thr1667Lys) | |
| 7 | g.128849379C= | CA1742564296 | FLNC | c.5000C= (p.Thr1667=) | |
| 7 | g.128849379C>G | CA369203964 | FLNC | c.5000C>G (p.Thr1667Arg) | ClinVar |
| 7 | g.128849379C>T | CA4475538 | FLNC | c.5000C>T (p.Thr1667Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128849380G>A | CA4475539 | FLNC | c.5001G>A (p.Thr1667=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128849380G>C | CA457849019 | FLNC | c.5001G>C (p.Thr1667=) | |
| 7 | g.128849380G= | CA1742564303 | FLNC | c.5001G= (p.Thr1667=) | |
| 7 | g.128849380G>T | CA457849020 | FLNC | c.5001G>T (p.Thr1667=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128849381G>A | CA369203967 | FLNC | c.5002G>A (p.Val1668Met) | gnomAD v4 |
| 7 | g.128849381G>C | CA369203965 | FLNC | c.5002G>C (p.Val1668Leu) | |
| 7 | g.128849381G>T | CA369203966 | FLNC | c.5002G>T (p.Val1668Leu) | |
| 7 | g.128849382T>A | CA369203968 | FLNC | c.5003T>A (p.Val1668Glu) | |
| 7 | g.128849382T>C | CA369203969 | FLNC | c.5003T>C (p.Val1668Ala) | gnomAD v4 |
| 7 | g.128849382T>G | CA369203970 | FLNC | c.5003T>G (p.Val1668Gly) | |
| 7 | g.128849383G>A | CA4475540 | FLNC | c.5004G>A (p.Val1668=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.128849383G>C | CA457849028 | FLNC | c.5004G>C (p.Val1668=) | |
| 7 | g.128849383G= | CA1742564307 | FLNC | c.5004G= (p.Val1668=) | |
| 7 | g.128849383G>T | CA457849030 | FLNC | c.5004G>T (p.Val1668=) | |
| 7 | g.128849384G>A | CA369203971 | FLNC | c.5005G>A (p.Asp1669Asn) | |
| 7 | g.128849384G>C | CA369203972 | FLNC | c.5005G>C (p.Asp1669His) | |
| 7 | g.128849384G>T | CA369203973 | FLNC | c.5005G>T (p.Asp1669Tyr) | |
| 7 | g.128849385A>C | CA369203974 | FLNC | c.5006A>C (p.Asp1669Ala) | |
| 7 | g.128849385A>G | CA369203975 | FLNC | c.5006A>G (p.Asp1669Gly) | |
| 7 | g.128849385A>T | CA369203976 | FLNC | c.5006A>T (p.Asp1669Val) | |
| 7 | g.128849386T>A | CA369203978 | FLNC | c.5007T>A (p.Asp1669Glu) | |
| 7 | g.128849386T>C | CA4475541 | FLNC | c.5007T>C (p.Asp1669=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128849386T>G | CA369203977 | FLNC | c.5007T>G (p.Asp1669Glu) | |
| 7 | g.128849386T= | CA1742564316 | FLNC | c.5007T= (p.Asp1669=) | |
| 7 | g.128849387G>A | CA369203979 | FLNC | c.5008G>A (p.Ala1670Thr) | |
| 7 | g.128849387G>C | CA369203980 | FLNC | c.5008G>C (p.Ala1670Pro) | gnomAD v4 |
| 7 | g.128849387G>T | CA369203981 | FLNC | c.5008G>T (p.Ala1670Ser) | COSMIC |
| 7 | g.128849388C>A | CA369203982 | FLNC | c.5009C>A (p.Ala1670Asp) | |
| 7 | g.128849388C>G | CA369203983 | FLNC | c.5009C>G (p.Ala1670Gly) | |
| 7 | g.128849388C>T | CA369203984 | FLNC | c.5009C>T (p.Ala1670Val) | |
| 7 | g.128849389C>A | CA457849052 | FLNC | c.5010C>A (p.Ala1670=) | |
| 7 | g.128849389C>G | CA457849054 | FLNC | c.5010C>G (p.Ala1670=) | |
| 7 | g.128849389C>T | CA457849056 | FLNC | c.5010C>T (p.Ala1670=) | |
| 7 | g.128849390A= | CA1742564319 | FLNC | c.5011A= (p.Lys1671=) | |
| 7 | g.128849390A>C | CA369203985 | FLNC | c.5011A>C (p.Lys1671Gln) | |
| 7 | g.128849390A>G | CA369203986 | FLNC | c.5011A>G (p.Lys1671Glu) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128849390A>T | CA369203987 | FLNC | c.5011A>T (p.Lys1671Ter) | gnomAD v4 |
| 7 | g.128849391A>C | CA369203988 | FLNC | c.5012A>C (p.Lys1671Thr) | |
| 7 | g.128849391A>G | CA369203989 | FLNC | c.5012A>G (p.Lys1671Arg) | |
| 7 | g.128849391A>T | CA369203990 | FLNC | c.5012A>T (p.Lys1671Met) | |
| 7 | g.128849392G>A | CA457849066 | FLNC | c.5013G>A (p.Lys1671=) | |
| 7 | g.128849392G>C | CA369203991 | FLNC | c.5013G>C (p.Lys1671Asn) | |
| 7 | g.128849392G= | CA1742564325 | FLNC | c.5013G= (p.Lys1671=) | |
| 7 | g.128849392G>T | CA4475542 | FLNC | c.5013G>T (p.Lys1671Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128849393G>A | CA4475543 | FLNC | c.5014G>A (p.Ala1672Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128849393G>C | CA369203992 | FLNC | c.5014G>C (p.Ala1672Pro) |