| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128838405A= | CA1742545094 | FLNC | c.1186A= (p.Thr396=) | |
| 7 | g.128838405A>C | CA369224284 | FLNC | c.1186A>C (p.Thr396Pro) | |
| 7 | g.128838405A>G | CA369224283 | FLNC | c.1186A>G (p.Thr396Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128838405A>T | CA369224282 | FLNC | c.1186A>T (p.Thr396Ser) | |
| 7 | g.128838406C>A | CA369224285 | FLNC | c.1187C>A (p.Thr396Asn) | ClinVar dbSNP |
| 7 | g.128838406C>G | CA369224286 | FLNC | c.1187C>G (p.Thr396Ser) | |
| 7 | g.128838406C>T | CA369224287 | FLNC | c.1187C>T (p.Thr396Ile) | |
| 7 | g.128838407C>A | CA457846435 | FLNC | c.1188C>A (p.Thr396=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128838407C= | CA1742545095 | FLNC | c.1188C= (p.Thr396=) | |
| 7 | g.128838407C>G | CA457846436 | FLNC | c.1188C>G (p.Thr396=) | |
| 7 | g.128838407C>T | CA457846437 | FLNC | c.1188C>T (p.Thr396=) | |
| 7 | g.128838407_128838413delinsCTACTTT | CA1742545096 | FLNC | c.1188_1194delinsCTACTTT (p.Thr396=) | |
| 7 | g.128838408T>A | CA369224288 | FLNC | c.1189T>A (p.Tyr397Asn) | |
| 7 | g.128838408T>C | CA369224289 | FLNC | c.1189T>C (p.Tyr397His) | |
| 7 | g.128838408T>G | CA369224290 | FLNC | c.1189T>G (p.Tyr397Asp) | |
| 7 | g.128838408_128838413del | CA1107056449 | FLNC | c.1189_1194del (p.Tyr397_Phe398del) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128838409A>C | CA369224293 | FLNC | c.1190A>C (p.Tyr397Ser) | |
| 7 | g.128838409A>G | CA369224291 | FLNC | c.1190A>G (p.Tyr397Cys) | |
| 7 | g.128838409A>T | CA369224292 | FLNC | c.1190A>T (p.Tyr397Phe) | |
| 7 | g.128838410C>A | CA369224294 | FLNC | c.1191C>A (p.Tyr397Ter) | |
| 7 | g.128838410C>G | CA369224295 | FLNC | c.1191C>G (p.Tyr397Ter) | |
| 7 | g.128838410C>T | CA457846439 | FLNC | c.1191C>T (p.Tyr397=) | |
| 7 | g.128838411T>A | CA369224296 | FLNC | c.1192T>A (p.Phe398Ile) | |
| 7 | g.128838411T>C | CA369224297 | FLNC | c.1192T>C (p.Phe398Leu) | |
| 7 | g.128838411T>G | CA369224298 | FLNC | c.1192T>G (p.Phe398Val) | |
| 7 | g.128838412T>A | CA369224299 | FLNC | c.1193T>A (p.Phe398Tyr) | |
| 7 | g.128838412T>C | CA369224301 | FLNC | c.1193T>C (p.Phe398Ser) | |
| 7 | g.128838412T>G | CA369224300 | FLNC | c.1193T>G (p.Phe398Cys) | |
| 7 | g.128838413T>A | CA369224302 | FLNC | c.1194T>A (p.Phe398Leu) | |
| 7 | g.128838413T>C | CA457846443 | FLNC | c.1194T>C (p.Phe398=) | |
| 7 | g.128838413T>G | CA369224303 | FLNC | c.1194T>G (p.Phe398Leu) | |
| 7 | g.128838414G>A | CA369224304 | FLNC | c.1195G>A (p.Asp399Asn) | |
| 7 | g.128838414G>C | CA369224305 | FLNC | c.1195G>C (p.Asp399His) | |
| 7 | g.128838414G>T | CA369224306 | FLNC | c.1195G>T (p.Asp399Tyr) | |
| 7 | g.128838415A>C | CA369224307 | FLNC | c.1196A>C (p.Asp399Ala) | |
| 7 | g.128838415A>G | CA369224308 | FLNC | c.1196A>G (p.Asp399Gly) | |
| 7 | g.128838415A>T | CA369224309 | FLNC | c.1196A>T (p.Asp399Val) | gnomAD v4 |
| 7 | g.128838418_128838423del | CA2695199636 | FLNC | c.1199_1204del (p.Ile400_Tyr401del) | ClinVar |
| 7 | g.128838416del | CA2684819871 | FLNC | c.1197del (p.Asp399GlufsTer15) | gnomAD v4 |
| 7 | g.128838416C>A | CA369224310 | FLNC | c.1197C>A (p.Asp399Glu) | |
| 7 | g.128838416C= | CA1742545097 | FLNC | c.1197C= (p.Asp399=) | |
| 7 | g.128838416C>G | CA369224311 | FLNC | c.1197C>G (p.Asp399Glu) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128838416C>T | CA4474254 | FLNC | c.1197C>T (p.Asp399=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128838417A>C | CA369224312 | FLNC | c.1198A>C (p.Ile400Leu) | |
| 7 | g.128838417A>G | CA369224314 | FLNC | c.1198A>G (p.Ile400Val) | |
| 7 | g.128838417A>T | CA369224313 | FLNC | c.1198A>T (p.Ile400Phe) | |
| 7 | g.128838418T>A | CA369224315 | FLNC | c.1199T>A (p.Ile400Asn) | |
| 7 | g.128838418T>C | CA369224317 | FLNC | c.1199T>C (p.Ile400Thr) | ClinVar dbSNP |
| 7 | g.128838418T>G | CA369224316 | FLNC | c.1199T>G (p.Ile400Ser) | |
| 7 | g.128838418T= | CA1742545098 | FLNC | c.1199T= (p.Ile400=) |