UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128844925G>A | CA369196977 | FLNC | c.3460G>A (p.Asp1154Asn) | |
| 7 | g.128844925G>C | CA369196979 | FLNC | c.3460G>C (p.Asp1154His) | |
| 7 | g.128844925G>T | CA369196981 | FLNC | c.3460G>T (p.Asp1154Tyr) | |
| 7 | g.128844926A>C | CA369196983 | FLNC | c.3461A>C (p.Asp1154Ala) | |
| 7 | g.128844926A>G | CA369196985 | FLNC | c.3461A>G (p.Asp1154Gly) | |
| 7 | g.128844926A>T | CA369196987 | FLNC | c.3461A>T (p.Asp1154Val) | |
| 7 | g.128844927C>A | CA369196989 | FLNC | c.3462C>A (p.Asp1154Glu) | |
| 7 | g.128844927C>G | CA369196991 | FLNC | c.3462C>G (p.Asp1154Glu) | |
| 7 | g.128844927C>T | CA457848299 | FLNC | c.3462C>T (p.Asp1154=) | |
| 7 | g.128844928C>A | CA369196992 | FLNC | c.3463C>A (p.Pro1155Thr) | |
| 7 | g.128844928C= | CA1742584476 | FLNC | c.3463C= (p.Pro1155=) | |
| 7 | g.128844928C>G | CA4475046 | FLNC | c.3463C>G (p.Pro1155Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128844928C>T | CA369196994 | FLNC | c.3463C>T (p.Pro1155Ser) | |
| 7 | g.128844929C>A | CA369196997 | FLNC | c.3464C>A (p.Pro1155Gln) | |
| 7 | g.128844929C= | CA1742584482 | FLNC | c.3464C= (p.Pro1155=) | |
| 7 | g.128844929C>G | CA369196999 | FLNC | c.3464C>G (p.Pro1155Arg) | dbSNP |
| 7 | g.128844929C>T | CA4475047 | FLNC | c.3464C>T (p.Pro1155Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128844930G>A | CA4475048 | FLNC | c.3465G>A (p.Pro1155=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128844930G>C | CA4475049 | FLNC | c.3465G>C (p.Pro1155=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128844930G= | CA1742584504 | FLNC | c.3465G= (p.Pro1155=) | |
| 7 | g.128844930G>T | CA457848303 | FLNC | c.3465G>T (p.Pro1155=) | ClinVar gnomAD v4 |
| 7 | g.128844930_128844932delinsAAA | CA2580614265 | FLNC | c.3465_3467delinsAAA (p.Ser1156Asn) | ClinVar |
| 7 | g.128844931A>C | CA369197004 | FLNC | c.3466A>C (p.Ser1156Arg) | |
| 7 | g.128844931A>G | CA369197006 | FLNC | c.3466A>G (p.Ser1156Gly) | |
| 7 | g.128844931A>T | CA369197008 | FLNC | c.3466A>T (p.Ser1156Cys) | |
| 7 | g.128844932G>A | CA4475050 | FLNC | c.3467G>A (p.Ser1156Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128844932G>C | CA369197011 | FLNC | c.3467G>C (p.Ser1156Thr) | |
| 7 | g.128844932G= | CA1742584514 | FLNC | c.3467G= (p.Ser1156=) | |
| 7 | g.128844932G>T | CA369197012 | FLNC | c.3467G>T (p.Ser1156Ile) | |
| 7 | g.128844933C>A | CA369197014 | FLNC | c.3468C>A (p.Ser1156Arg) | |
| 7 | g.128844933C= | CA1742584522 | FLNC | c.3468C= (p.Ser1156=) | |
| 7 | g.128844933C>G | CA369197016 | FLNC | c.3468C>G (p.Ser1156Arg) | |
| 7 | g.128844933C>T | CA457848305 | FLNC | c.3468C>T (p.Ser1156=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128844934A= | CA1742584528 | FLNC | c.3469A= (p.Lys1157=) | |
| 7 | g.128844934A>C | CA369197018 | FLNC | c.3469A>C (p.Lys1157Gln) | dbSNP |
| 7 | g.128844934A>G | CA369197020 | FLNC | c.3469A>G (p.Lys1157Glu) | |
| 7 | g.128844934A>T | CA369197022 | FLNC | c.3469A>T (p.Lys1157Ter) | |
| 7 | g.128844935A>C | CA369197024 | FLNC | c.3470A>C (p.Lys1157Thr) | |
| 7 | g.128844935A>G | CA369197025 | FLNC | c.3470A>G (p.Lys1157Arg) | |
| 7 | g.128844935A>T | CA369197027 | FLNC | c.3470A>T (p.Lys1157Met) | |
| 7 | g.128844936G>A | CA457848307 | FLNC | c.3471G>A (p.Lys1157=) | |
| 7 | g.128844936G>C | CA369197028 | FLNC | c.3471G>C (p.Lys1157Asn) | |
| 7 | g.128844936G>T | CA369197030 | FLNC | c.3471G>T (p.Lys1157Asn) | |
| 7 | g.128844937G>A | CA369197032 | FLNC | c.3472G>A (p.Val1158Met) | |
| 7 | g.128844937G>C | CA369197034 | FLNC | c.3472G>C (p.Val1158Leu) | |
| 7 | g.128844937G>T | CA369197036 | FLNC | c.3472G>T (p.Val1158Leu) | ClinVar gnomAD v4 |
| 7 | g.128844938T>A | CA369197039 | FLNC | c.3473T>A (p.Val1158Glu) | |
| 7 | g.128844938T>C | CA369197040 | FLNC | c.3473T>C (p.Val1158Ala) | dbSNP gnomAD v2 |
| 7 | g.128844938T>G | CA369197042 | FLNC | c.3473T>G (p.Val1158Gly) | COSMIC |
| 7 | g.128844938T= | CA1742584534 | FLNC | c.3473T= (p.Val1158=) | |
| 7 | g.128844939G>A | CA457848312 | FLNC | c.3474G>A (p.Val1158=) | |
| 7 | g.128844939G>C | CA457848311 | FLNC | c.3474G>C (p.Val1158=) | |
| 7 | g.128844939G>T | CA457848313 | FLNC | c.3474G>T (p.Val1158=) | |
| 7 | g.128844940C>A | CA457848314 | FLNC | c.3475C>A (p.Arg1159=) | gnomAD v4 |
| 7 | g.128844940C= | CA1742584544 | FLNC | c.3475C= (p.Arg1159=) | |
| 7 | g.128844940C>G | CA166178646 | FLNC | c.3475C>G (p.Arg1159Gly) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128844940C>T | CA4475051 | FLNC | c.3475C>T (p.Arg1159Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128844941G>A | CA4475052 | FLNC | c.3476G>A (p.Arg1159Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128844941G>C | CA369197048 | FLNC | c.3476G>C (p.Arg1159Pro) | |
| 7 | g.128844941G= | CA1742584548 | FLNC | c.3476G= (p.Arg1159=) | |
| 7 | g.128844941G>T | CA369197050 | FLNC | c.3476G>T (p.Arg1159Leu) | |
| 7 | g.128844943del | CA2684818416 | FLNC | c.3478del (p.Ala1160ProfsTer29) | gnomAD v4 |
| 7 | g.128844942G>A | CA457848317 | FLNC | c.3477G>A (p.Arg1159=) | |
| 7 | g.128844942G>C | CA457848318 | FLNC | c.3477G>C (p.Arg1159=) | |
| 7 | g.128844942G>T | CA457848319 | FLNC | c.3477G>T (p.Arg1159=) | COSMIC |
| 7 | g.128844943G>A | CA369197052 | FLNC | c.3478G>A (p.Ala1160Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128844943G>C | CA369197054 | FLNC | c.3478G>C (p.Ala1160Pro) | |
| 7 | g.128844943G= | CA1742584558 | FLNC | c.3478G= (p.Ala1160=) | |
| 7 | g.128844943G>T | CA369197056 | FLNC | c.3478G>T (p.Ala1160Ser) | |
| 7 | g.128844944C>A | CA369197058 | FLNC | c.3479C>A (p.Ala1160Asp) | |
| 7 | g.128844944C>G | CA369197060 | FLNC | c.3479C>G (p.Ala1160Gly) | |
| 7 | g.128844944C>T | CA369197061 | FLNC | c.3479C>T (p.Ala1160Val) | |
| 7 | g.128844945C>A | CA457848322 | FLNC | c.3480C>A (p.Ala1160=) | |
| 7 | g.128844945C>G | CA457848324 | FLNC | c.3480C>G (p.Ala1160=) | |
| 7 | g.128844945C>T | CA457848323 | FLNC | c.3480C>T (p.Ala1160=) | gnomAD v4 |
| 7 | g.128844946A= | CA1742584560 | FLNC | c.3481A= (p.Ser1161=) | |
| 7 | g.128844946A>C | CA369197064 | FLNC | c.3481A>C (p.Ser1161Arg) | |
| 7 | g.128844946A>G | CA4475053 | FLNC | c.3481A>G (p.Ser1161Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128844946A>T | CA369197067 | FLNC | c.3481A>T (p.Ser1161Cys) | |
| 7 | g.128844947G>A | CA369197072 | FLNC | c.3482G>A (p.Ser1161Asn) | gnomAD v4 |
| 7 | g.128844947G>C | CA369197070 | FLNC | c.3482G>C (p.Ser1161Thr) | |
| 7 | g.128844947G>T | CA369197068 | FLNC | c.3482G>T (p.Ser1161Ile) | |
| 7 | g.128844947_128844948delinsTC | CA2580076614 | FLNC | c.3482_3483delinsTC (p.Ser1161Ile) | ClinVar |
| 7 | g.128844948T>A | CA369197076 | FLNC | c.3483T>A (p.Ser1161Arg) | |
| 7 | g.128844948T>C | CA457848327 | FLNC | c.3483T>C (p.Ser1161=) | ClinVar gnomAD v4 |
| 7 | g.128844948T>G | CA369197074 | FLNC | c.3483T>G (p.Ser1161Arg) | |
| 7 | g.128844949G>A | CA369197081 | FLNC | c.3484G>A (p.Gly1162Arg) | |
| 7 | g.128844949G>C | CA369197078 | FLNC | c.3484G>C (p.Gly1162Arg) | |
| 7 | g.128844949G>T | CA369197079 | FLNC | c.3484G>T (p.Gly1162Ter) | |
| 7 | g.128844950G>A | CA369197084 | FLNC | c.3485G>A (p.Gly1162Glu) | COSMIC |
| 7 | g.128844950G>C | CA369197085 | FLNC | c.3485G>C (p.Gly1162Ala) | |
| 7 | g.128844950G>T | CA369197086 | FLNC | c.3485G>T (p.Gly1162Val) | |
| 7 | g.128844951A>C | CA457848330 | FLNC | c.3486A>C (p.Gly1162=) | |
| 7 | g.128844951A>G | CA457848331 | FLNC | c.3486A>G (p.Gly1162=) | |
| 7 | g.128844951A>T | CA457848332 | FLNC | c.3486A>T (p.Gly1162=) | |
| 7 | g.128844952C>A | CA369197087 | FLNC | c.3487C>A (p.Pro1163Thr) | COSMIC |
| 7 | g.128844952C= | CA1742584564 | FLNC | c.3487C= (p.Pro1163=) | |
| 7 | g.128844952C>G | CA369197088 | FLNC | c.3487C>G (p.Pro1163Ala) | |
| 7 | g.128844952C>T | CA369197089 | FLNC | c.3487C>T (p.Pro1163Ser) | dbSNP |
| 7 | g.128844953C>A | CA369197090 | FLNC | c.3488C>A (p.Pro1163Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128844953C= | CA1742584573 | FLNC | c.3488C= (p.Pro1163=) | |
| 7 | g.128844953C>G | CA369197091 | FLNC | c.3488C>G (p.Pro1163Arg) | gnomAD v4 |
| 7 | g.128844953C>T | CA4475054 | FLNC | c.3488C>T (p.Pro1163Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128844954G>A | CA457848337 | FLNC | c.3489G>A (p.Pro1163=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128844954G>C | CA4475055 | FLNC | c.3489G>C (p.Pro1163=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128844954G= | CA1742584584 | FLNC | c.3489G= (p.Pro1163=) | |
| 7 | g.128844954G>T | CA457848336 | FLNC | c.3489G>T (p.Pro1163=) | |
| 7 | g.128844955G>A | CA369197093 | FLNC | c.3490G>A (p.Gly1164Ser) | |
| 7 | g.128844955G>C | CA369197094 | FLNC | c.3490G>C (p.Gly1164Arg) | |
| 7 | g.128844955G>T | CA369197092 | FLNC | c.3490G>T (p.Gly1164Cys) | COSMIC |
| 7 | g.128844956G>A | CA369197095 | FLNC | c.3491G>A (p.Gly1164Asp) | |
| 7 | g.128844956G>C | CA369197096 | FLNC | c.3491G>C (p.Gly1164Ala) | |
| 7 | g.128844956G>T | CA369197097 | FLNC | c.3491G>T (p.Gly1164Val) | |
| 7 | g.128844957C>A | CA457848340 | FLNC | c.3492C>A (p.Gly1164=) | |
| 7 | g.128844957C>G | CA457848341 | FLNC | c.3492C>G (p.Gly1164=) | |
| 7 | g.128844957C>T | CA457848342 | FLNC | c.3492C>T (p.Gly1164=) | |
| 7 | g.128844958C>A | CA369197098 | FLNC | c.3493C>A (p.Leu1165Met) | |
| 7 | g.128844958C>G | CA369197099 | FLNC | c.3493C>G (p.Leu1165Val) | |
| 7 | g.128844958C>T | CA457848343 | FLNC | c.3493C>T (p.Leu1165=) | |
| 7 | g.128844959T>A | CA369197102 | FLNC | c.3494T>A (p.Leu1165Gln) | |
| 7 | g.128844959T>C | CA369197100 | FLNC | c.3494T>C (p.Leu1165Pro) | |
| 7 | g.128844959T>G | CA369197101 | FLNC | c.3494T>G (p.Leu1165Arg) | |
| 7 | g.128844960G>A | CA457848347 | FLNC | c.3495G>A (p.Leu1165=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128844960G>C | CA457848345 | FLNC | c.3495G>C (p.Leu1165=) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128844960G= | CA1742584593 | FLNC | c.3495G= (p.Leu1165=) | |
| 7 | g.128844960G>T | CA457848346 | FLNC | c.3495G>T (p.Leu1165=) | |
| 7 | g.128844961G>A | CA369197103 | FLNC | c.3496G>A (p.Glu1166Lys) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128844961G>C | CA369197104 | FLNC | c.3496G>C (p.Glu1166Gln) | |
| 7 | g.128844961G= | CA1742584598 | FLNC | c.3496G= (p.Glu1166=) | |
| 7 | g.128844961G>T | CA369197105 | FLNC | c.3496G>T (p.Glu1166Ter) | |
| 7 | g.128844962A>C | CA369197106 | FLNC | c.3497A>C (p.Glu1166Ala) | |
| 7 | g.128844962A>G | CA369197107 | FLNC | c.3497A>G (p.Glu1166Gly) | |
| 7 | g.128844962A>T | CA369197108 | FLNC | c.3497A>T (p.Glu1166Val) | |
| 7 | g.128844963G>A | CA457848351 | FLNC | c.3498G>A (p.Glu1166=) | |
| 7 | g.128844963G>C | CA369197109 | FLNC | c.3498G>C (p.Glu1166Asp) | gnomAD v4 |
| 7 | g.128844963G>T | CA369197110 | FLNC | c.3498G>T (p.Glu1166Asp) | |
| 7 | g.128844964C>A | CA369197111 | FLNC | c.3499C>A (p.Arg1167Ser) | ClinVar gnomAD v4 |
| 7 | g.128844964C= | CA1742584612 | FLNC | c.3499C= (p.Arg1167=) | |
| 7 | g.128844964C>G | CA369197112 | FLNC | c.3499C>G (p.Arg1167Gly) | |
| 7 | g.128844964C>T | CA4475056 | FLNC | c.3499C>T (p.Arg1167Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128844965G>A | CA4475057 | FLNC | c.3500G>A (p.Arg1167His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128844965G>C | CA369197113 | FLNC | c.3500G>C (p.Arg1167Pro) | gnomAD v4 |
| 7 | g.128844965G= | CA1742584624 | FLNC | c.3500G= (p.Arg1167=) | |
| 7 | g.128844965G>T | CA369197114 | FLNC | c.3500G>T (p.Arg1167Leu) | |
| 7 | g.128844966C>A | CA457848353 | FLNC | c.3501C>A (p.Arg1167=) | |
| 7 | g.128844966C= | CA1742584629 | FLNC | c.3501C= (p.Arg1167=) | |
| 7 | g.128844966C>G | CA457848354 | FLNC | c.3501C>G (p.Arg1167=) | |
| 7 | g.128844966C>T | CA4475058 | FLNC | c.3501C>T (p.Arg1167=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128844967G>A | CA4475059 | FLNC | c.3502G>A (p.Gly1168Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128844967G>C | CA369197115 | FLNC | c.3502G>C (p.Gly1168Arg) | |
| 7 | g.128844967G= | CA1742584637 | FLNC | c.3502G= (p.Gly1168=) | |
| 7 | g.128844967G>T | CA369197116 | FLNC | c.3502G>T (p.Gly1168Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128844968G>A | CA369197117 | FLNC | c.3503G>A (p.Gly1168Asp) | ClinVar COSMIC |
| 7 | g.128844968G>C | CA369197118 | FLNC | c.3503G>C (p.Gly1168Ala) | |
| 7 | g.128844968G>T | CA369197119 | FLNC | c.3503G>T (p.Gly1168Val) | |
| 7 | g.128844969C>A | CA457848357 | FLNC | c.3504C>A (p.Gly1168=) | |
| 7 | g.128844969C>G | CA457848358 | FLNC | c.3504C>G (p.Gly1168=) | |
| 7 | g.128844969C>T | CA457848356 | FLNC | c.3504C>T (p.Gly1168=) | ClinVar gnomAD v4 |
| 7 | g.128844970A>C | CA369197121 | FLNC | c.3505A>C (p.Lys1169Gln) | |
| 7 | g.128844970A>G | CA369197122 | FLNC | c.3505A>G (p.Lys1169Glu) | |
| 7 | g.128844970A>T | CA369197120 | FLNC | c.3505A>T (p.Lys1169Ter) | |
| 7 | g.128844971A= | CA1742584643 | FLNC | c.3506A= (p.Lys1169=) | |
| 7 | g.128844971A>C | CA369197123 | FLNC | c.3506A>C (p.Lys1169Thr) | |
| 7 | g.128844971A>G | CA4475060 | FLNC | c.3506A>G (p.Lys1169Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128844971A>T | CA4475061 | FLNC | c.3506A>T (p.Lys1169Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128844972G>A | CA4475062 | FLNC | c.3507G>A (p.Lys1169=) | ClinVar dbSNP ExAC gnomAD v2 |
| 7 | g.128844972G>C | CA369197124 | FLNC | c.3507G>C (p.Lys1169Asn) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128844972G= | CA1742584652 | FLNC | c.3507G= (p.Lys1169=) | |
| 7 | g.128844972G>T | CA369197125 | FLNC | c.3507G>T (p.Lys1169Asn) | |
| 7 | g.128844973G>A | CA369197126 | FLNC | c.3508G>A (p.Val1170Ile) | gnomAD v4 |
| 7 | g.128844973G>C | CA369197128 | FLNC | c.3508G>C (p.Val1170Leu) | |
| 7 | g.128844973G>T | CA369197127 | FLNC | c.3508G>T (p.Val1170Phe) | |
| 7 | g.128844974T>A | CA369197129 | FLNC | c.3509T>A (p.Val1170Asp) | |
| 7 | g.128844974T>C | CA369197130 | FLNC | c.3509T>C (p.Val1170Ala) | |
| 7 | g.128844974T>G | CA369197131 | FLNC | c.3509T>G (p.Val1170Gly) | |
| 7 | g.128844975C>A | CA457848362 | FLNC | c.3510C>A (p.Val1170=) | |
| 7 | g.128844975C= | CA1742584660 | FLNC | c.3510C= (p.Val1170=) | |
| 7 | g.128844975C>G | CA457848363 | FLNC | c.3510C>G (p.Val1170=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128844975C>T | CA4475063 | FLNC | c.3510C>T (p.Val1170=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128844976G>A | CA4475064 | FLNC | c.3511G>A (p.Gly1171Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128844976G>C | CA369197133 | FLNC | c.3511G>C (p.Gly1171Arg) | gnomAD v4 |
| 7 | g.128844976G= | CA1742584680 | FLNC | c.3511G= (p.Gly1171=) | |
| 7 | g.128844976G>T | CA369197132 | FLNC | c.3511G>T (p.Gly1171Cys) | ClinVar dbSNP |
| 7 | g.128844977G>A | CA369197134 | FLNC | c.3512G>A (p.Gly1171Asp) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128844977G>C | CA369197136 | FLNC | c.3512G>C (p.Gly1171Ala) | |
| 7 | g.128844977G= | CA1742584692 | FLNC | c.3512G= (p.Gly1171=) | |
| 7 | g.128844977G>T | CA369197135 | FLNC | c.3512G>T (p.Gly1171Val) | ClinVar |
| 7 | g.128844978T>A | CA457848367 | FLNC | c.3513T>A (p.Gly1171=) | |
| 7 | g.128844978T>C | CA457848368 | FLNC | c.3513T>C (p.Gly1171=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128844978T>G | CA457848369 | FLNC | c.3513T>G (p.Gly1171=) | |
| 7 | g.128844978T= | CA1742584698 | FLNC | c.3513T= (p.Gly1171=) | |
| 7 | g.128844979G>A | CA369197137 | FLNC | c.3514G>A (p.Glu1172Lys) | COSMIC |
| 7 | g.128844979G>C | CA369197138 | FLNC | c.3514G>C (p.Glu1172Gln) | |
| 7 | g.128844979G>T | CA369197139 | FLNC | c.3514G>T (p.Glu1172Ter) | |
| 7 | g.128844980A>C | CA369197140 | FLNC | c.3515A>C (p.Glu1172Ala) | |
| 7 | g.128844980A>G | CA369197141 | FLNC | c.3515A>G (p.Glu1172Gly) | |
| 7 | g.128844980A>T | CA369197142 | FLNC | c.3515A>T (p.Glu1172Val) | |
| 7 | g.128844981G>A | CA457848372 | FLNC | c.3516G>A (p.Glu1172=) | |
| 7 | g.128844981G>C | CA369197143 | FLNC | c.3516G>C (p.Glu1172Asp) | |
| 7 | g.128844981G= | CA1742584703 | FLNC | c.3516G= (p.Glu1172=) | |
| 7 | g.128844981G>T | CA4475065 | FLNC | c.3516G>T (p.Glu1172Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.128844982G>A | CA369197144 | FLNC | c.3517G>A (p.Ala1173Thr) | |
| 7 | g.128844982G>C | CA369197145 | FLNC | c.3517G>C (p.Ala1173Pro) | |
| 7 | g.128844982G>T | CA369197146 | FLNC | c.3517G>T (p.Ala1173Ser) | |
| 7 | g.128844983C>A | CA369197149 | FLNC | c.3518C>A (p.Ala1173Glu) | |
| 7 | g.128844983C= | CA1742584715 | FLNC | c.3518C= (p.Ala1173=) | |
| 7 | g.128844983C>G | CA369197148 | FLNC | c.3518C>G (p.Ala1173Gly) | dbSNP |
| 7 | g.128844983C>T | CA369197147 | FLNC | c.3518C>T (p.Ala1173Val) | ClinVar dbSNP |
| 7 | g.128844984A>C | CA457848377 | FLNC | c.3519A>C (p.Ala1173=) | |
| 7 | g.128844984A>G | CA457848378 | FLNC | c.3519A>G (p.Ala1173=) | |
| 7 | g.128844984A>T | CA457848379 | FLNC | c.3519A>T (p.Ala1173=) | |
| 7 | g.128844985G>A | CA369197150 | FLNC | c.3520G>A (p.Ala1174Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128844985G>C | CA369197151 | FLNC | c.3520G>C (p.Ala1174Pro) | |
| 7 | g.128844985G= | CA1742584734 | FLNC | c.3520G= (p.Ala1174=) | |
| 7 | g.128844985G>T | CA369197152 | FLNC | c.3520G>T (p.Ala1174Ser) | |
| 7 | g.128844986C>A | CA369197153 | FLNC | c.3521C>A (p.Ala1174Asp) | |
| 7 | g.128844986C>G | CA369197154 | FLNC | c.3521C>G (p.Ala1174Gly) | |
| 7 | g.128844986C>T | CA369197155 | FLNC | c.3521C>T (p.Ala1174Val) | |
| 7 | g.128844987C>A | CA457848383 | FLNC | c.3522C>A (p.Ala1174=) | dbSNP gnomAD v2 |
| 7 | g.128844987C= | CA1742584740 | FLNC | c.3522C= (p.Ala1174=) | |
| 7 | g.128844987C>G | CA457848384 | FLNC | c.3522C>G (p.Ala1174=) | |
| 7 | g.128844987C>T | CA457848385 | FLNC | c.3522C>T (p.Ala1174=) | |
| 7 | g.128844988A= | CA1742584745 | FLNC | c.3523A= (p.Thr1175=) | |
| 7 | g.128844988A>C | CA369197156 | FLNC | c.3523A>C (p.Thr1175Pro) | |
| 7 | g.128844988A>G | CA369197157 | FLNC | c.3523A>G (p.Thr1175Ala) | dbSNP |
| 7 | g.128844988A>T | CA369197158 | FLNC | c.3523A>T (p.Thr1175Ser) | |
| 7 | g.128844989C>A | CA369197159 | FLNC | c.3524C>A (p.Thr1175Asn) | |
| 7 | g.128844989C= | CA1742584750 | FLNC | c.3524C= (p.Thr1175=) | |
| 7 | g.128844989C>G | CA369197160 | FLNC | c.3524C>G (p.Thr1175Ser) | dbSNP |
| 7 | g.128844989C>T | CA369197161 | FLNC | c.3524C>T (p.Thr1175Ile) | |
| 7 | g.128844990C>A | CA457848389 | FLNC | c.3525C>A (p.Thr1175=) | |
| 7 | g.128844990C= | CA1742584751 | FLNC | c.3525C= (p.Thr1175=) | |
| 7 | g.128844990C>G | CA457848390 | FLNC | c.3525C>G (p.Thr1175=) | |
| 7 | g.128844990C>T | CA457848391 | FLNC | c.3525C>T (p.Thr1175=) | dbSNP |
| 7 | g.128844991T>A | CA369197164 | FLNC | c.3526T>A (p.Phe1176Ile) | |
| 7 | g.128844991T>C | CA369197163 | FLNC | c.3526T>C (p.Phe1176Leu) | |
| 7 | g.128844991T>G | CA369197162 | FLNC | c.3526T>G (p.Phe1176Val) | |
| 7 | g.128844992T>A | CA369197165 | FLNC | c.3527T>A (p.Phe1176Tyr) | |
| 7 | g.128844992T>C | CA369197166 | FLNC | c.3527T>C (p.Phe1176Ser) | |
| 7 | g.128844992T>G | CA369197167 | FLNC | c.3527T>G (p.Phe1176Cys) | |
| 7 | g.128844993C>A | CA369197168 | FLNC | c.3528C>A (p.Phe1176Leu) | |
| 7 | g.128844993C= | CA1742584755 | FLNC | c.3528C= (p.Phe1176=) | |
| 7 | g.128844993C>G | CA369197169 | FLNC | c.3528C>G (p.Phe1176Leu) | |
| 7 | g.128844993C>T | CA457848392 | FLNC | c.3528C>T (p.Phe1176=) | dbSNP gnomAD v2 |
| 7 | g.128844994A= | CA1742584761 | FLNC | c.3529A= (p.Thr1177=) | |
| 7 | g.128844994A>C | CA369197171 | FLNC | c.3529A>C (p.Thr1177Pro) | |
| 7 | g.128844994A>G | CA4475066 | FLNC | c.3529A>G (p.Thr1177Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128844994A>T | CA369197170 | FLNC | c.3529A>T (p.Thr1177Ser) | COSMIC |
| 7 | g.128844995C>A | CA369197172 | FLNC | c.3530C>A (p.Thr1177Asn) | |
| 7 | g.128844995C>G | CA369197173 | FLNC | c.3530C>G (p.Thr1177Ser) | dbSNP gnomAD v4 |
| 7 | g.128844995C>T | CA369197174 | FLNC | c.3530C>T (p.Thr1177Ile) | |
| 7 | g.128844996T>A | CA457848398 | FLNC | c.3531T>A (p.Thr1177=) | |
| 7 | g.128844996T>C | CA457848396 | FLNC | c.3531T>C (p.Thr1177=) | |
| 7 | g.128844996T>G | CA457848397 | FLNC | c.3531T>G (p.Thr1177=) | gnomAD v4 |
| 7 | g.128844997G>A | CA369197175 | FLNC | c.3532G>A (p.Val1178Met) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128844997G>C | CA369197176 | FLNC | c.3532G>C (p.Val1178Leu) | |
| 7 | g.128844997G= | CA1742584769 | FLNC | c.3532G= (p.Val1178=) | |
| 7 | g.128844997G>T | CA369197177 | FLNC | c.3532G>T (p.Val1178Leu) | |
| 7 | g.128844998T>A | CA369197178 | FLNC | c.3533T>A (p.Val1178Glu) | |
| 7 | g.128844998T>C | CA369197180 | FLNC | c.3533T>C (p.Val1178Ala) | |
| 7 | g.128844998T>G | CA369197179 | FLNC | c.3533T>G (p.Val1178Gly) | |
| 7 | g.128844999G>A | CA457848401 | FLNC | c.3534G>A (p.Val1178=) | |
| 7 | g.128844999G>C | CA457848403 | FLNC | c.3534G>C (p.Val1178=) | |
| 7 | g.128844999G>T | CA457848404 | FLNC | c.3534G>T (p.Val1178=) | |
| 7 | g.128845000G>A | CA369197181 | FLNC | c.3535G>A (p.Asp1179Asn) | |
| 7 | g.128845000G>C | CA369197182 | FLNC | c.3535G>C (p.Asp1179His) | |
| 7 | g.128845000G>T | CA369197183 | FLNC | c.3535G>T (p.Asp1179Tyr) | |
| 7 | g.128845001A>C | CA369197184 | FLNC | c.3536A>C (p.Asp1179Ala) | |
| 7 | g.128845001A>G | CA369197185 | FLNC | c.3536A>G (p.Asp1179Gly) | |
| 7 | g.128845001A>T | CA369197186 | FLNC | c.3536A>T (p.Asp1179Val) | gnomAD v4 |
| 7 | g.128845002C>A | CA369197187 | FLNC | c.3537C>A (p.Asp1179Glu) | |
| 7 | g.128845002C>G | CA369197188 | FLNC | c.3537C>G (p.Asp1179Glu) | |
| 7 | g.128845002C>T | CA457848409 | FLNC | c.3537C>T (p.Asp1179=) | gnomAD v4 |
| 7 | g.128845003T>A | CA369197189 | FLNC | c.3538T>A (p.Cys1180Ser) | |
| 7 | g.128845003T>C | CA369197190 | FLNC | c.3538T>C (p.Cys1180Arg) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128845003T>G | CA369197191 | FLNC | c.3538T>G (p.Cys1180Gly) | |
| 7 | g.128845003T= | CA1742584772 | FLNC | c.3538T= (p.Cys1180=) | |
| 7 | g.128845004G>A | CA369197193 | FLNC | c.3539G>A (p.Cys1180Tyr) | |
| 7 | g.128845004G>C | CA369197194 | FLNC | c.3539G>C (p.Cys1180Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128845004G= | CA1742584776 | FLNC | c.3539G= (p.Cys1180=) | |
| 7 | g.128845004G>T | CA369197192 | FLNC | c.3539G>T (p.Cys1180Phe) | ClinVar dbSNP |
| 7 | g.128845004_128845005insGGTA | CA2684818470 | FLNC | c.3539_3540insGGTA (p.Cys1180TrpfsTer13) | gnomAD v4 |
| 7 | g.128845005C>A | CA369197195 | FLNC | c.3540C>A (p.Cys1180Ter) | |
| 7 | g.128845005C= | CA1742584780 | FLNC | c.3540C= (p.Cys1180=) | |
| 7 | g.128845005C>G | CA369197196 | FLNC | c.3540C>G (p.Cys1180Trp) | |
| 7 | g.128845005C>T | CA457848413 | FLNC | c.3540C>T (p.Cys1180=) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128845006T>A | CA369197197 | FLNC | c.3541T>A (p.Ser1181Thr) | |
| 7 | g.128845006T>C | CA369197198 | FLNC | c.3541T>C (p.Ser1181Pro) | ClinVar dbSNP |
| 7 | g.128845006T>G | CA369197199 | FLNC | c.3541T>G (p.Ser1181Ala) | |
| 7 | g.128845007C>A | CA369197200 | FLNC | c.3542C>A (p.Ser1181Ter) | |
| 7 | g.128845007C>G | CA369197201 | FLNC | c.3542C>G (p.Ser1181Ter) | |
| 7 | g.128845007C>T | CA369197202 | FLNC | c.3542C>T (p.Ser1181Leu) | |
| 7 | g.128845008_128845009insCAGCGACATGCACCTGCCA | CA2684818471 | FLNC | c.3543_3544insCAGCGACATGCACCTGCCA (p.Glu1182GlnfsTer16) | gnomAD v4 |
| 7 | g.128845008A= | CA1742584785 | FLNC | c.3543A= (p.Ser1181=) | |
| 7 | g.128845008A>C | CA457848415 | FLNC | c.3543A>C (p.Ser1181=) | |
| 7 | g.128845008A>G | CA166178712 | FLNC | c.3543A>G (p.Ser1181=) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.128845008A>T | CA457848416 | FLNC | c.3543A>T (p.Ser1181=) | |
| 7 | g.128845009G>A | CA369197203 | FLNC | c.3544G>A (p.Glu1182Lys) | |
| 7 | g.128845009G>C | CA369197204 | FLNC | c.3544G>C (p.Glu1182Gln) | |
| 7 | g.128845009G>T | CA369197205 | FLNC | c.3544G>T (p.Glu1182Ter) | |
| 7 | g.128845010A>C | CA369197206 | FLNC | c.3545A>C (p.Glu1182Ala) | |
| 7 | g.128845010A>G | CA369197207 | FLNC | c.3545A>G (p.Glu1182Gly) | |
| 7 | g.128845010A>T | CA369197208 | FLNC | c.3545A>T (p.Glu1182Val) | |
| 7 | g.128845011G>A | CA457848417 | FLNC | c.3546G>A (p.Glu1182=) | |
| 7 | g.128845011G>C | CA369197210 | FLNC | c.3546G>C (p.Glu1182Asp) | |
| 7 | g.128845011G>T | CA369197209 | FLNC | c.3546G>T (p.Glu1182Asp) | |
| 7 | g.128845012G>A | CA369197211 | FLNC | c.3547G>A (p.Ala1183Thr) | |
| 7 | g.128845012G>C | CA369197212 | FLNC | c.3547G>C (p.Ala1183Pro) | |
| 7 | g.128845012G>T | CA369197213 | FLNC | c.3547G>T (p.Ala1183Ser) | gnomAD v4 |
| 7 | g.128845012_128845013delinsCT | CA645372843 | FLNC | c.3547_3548delinsCT (p.Ala1183Leu) | ClinVar dbSNP |
| 7 | g.128845012_128845013delinsGC | CA1742584790 | FLNC | c.3547_3548delinsGC (p.Ala1183=) | |
| 7 | g.128845013C>A | CA369197214 | FLNC | c.3548C>A (p.Ala1183Glu) | |
| 7 | g.128845013C>G | CA369197215 | FLNC | c.3548C>G (p.Ala1183Gly) | |
| 7 | g.128845013C>T | CA369197216 | FLNC | c.3548C>T (p.Ala1183Val) | ClinVar |
| 7 | g.128845014A>C | CA457848421 | FLNC | c.3549A>C (p.Ala1183=) | |
| 7 | g.128845014A>G | CA457848422 | FLNC | c.3549A>G (p.Ala1183=) | |
| 7 | g.128845014A>T | CA457848423 | FLNC | c.3549A>T (p.Ala1183=) | |
| 7 | g.128845015G>A | CA369197219 | FLNC | c.3550G>A (p.Gly1184Ser) | |
| 7 | g.128845015G>C | CA369197217 | FLNC | c.3550G>C (p.Gly1184Arg) | |
| 7 | g.128845015G>T | CA369197218 | FLNC | c.3550G>T (p.Gly1184Cys) | |
| 7 | g.128845016G>A | CA369197220 | FLNC | c.3551G>A (p.Gly1184Asp) | ClinVar dbSNP |
| 7 | g.128845016G>C | CA369197221 | FLNC | c.3551G>C (p.Gly1184Ala) | |
| 7 | g.128845016G>T | CA369197222 | FLNC | c.3551G>T (p.Gly1184Val) | ClinVar |
| 7 | g.128845017C>A | CA457848426 | FLNC | c.3552C>A (p.Gly1184=) | dbSNP gnomAD v4 |
| 7 | g.128845017C= | CA1742584801 | FLNC | c.3552C= (p.Gly1184=) | |
| 7 | g.128845017C>G | CA4475067 | FLNC | c.3552C>G (p.Gly1184=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128845017C>T | CA166178715 | FLNC | c.3552C>T (p.Gly1184=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.128845018G>A | CA16605647 | FLNC | c.3553G>A (p.Glu1185Lys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128845018G>C | CA369197223 | FLNC | c.3553G>C (p.Glu1185Gln) | |
| 7 | g.128845018G= | CA1742584806 | FLNC | c.3553G= (p.Glu1185=) | |
| 7 | g.128845018G>T | CA369197224 | FLNC | c.3553G>T (p.Glu1185Ter) | |
| 7 | g.128845019A>C | CA369197225 | FLNC | c.3554A>C (p.Glu1185Ala) | |
| 7 | g.128845019A>G | CA369197226 | FLNC | c.3554A>G (p.Glu1185Gly) | |
| 7 | g.128845019A>T | CA369197227 | FLNC | c.3554A>T (p.Glu1185Val) | |
| 7 | g.128845020G>A | CA457848430 | FLNC | c.3555G>A (p.Glu1185=) | |
| 7 | g.128845020G>C | CA369197228 | FLNC | c.3555G>C (p.Glu1185Asp) | |
| 7 | g.128845020G>T | CA369197229 | FLNC | c.3555G>T (p.Glu1185Asp) | |
| 7 | g.128845021G>A | CA369197230 | FLNC | c.3556G>A (p.Ala1186Thr) | dbSNP gnomAD v4 |
| 7 | g.128845021G>C | CA369197231 | FLNC | c.3556G>C (p.Ala1186Pro) | |
| 7 | g.128845021G= | CA1742584816 | FLNC | c.3556G= (p.Ala1186=) | |
| 7 | g.128845021G>T | CA369197232 | FLNC | c.3556G>T (p.Ala1186Ser) | |
| 7 | g.128845022C>A | CA369197233 | FLNC | c.3557C>A (p.Ala1186Glu) | |
| 7 | g.128845022C= | CA1742584817 | FLNC | c.3557C= (p.Ala1186=) | |
| 7 | g.128845022C>G | CA369197235 | FLNC | c.3557C>G (p.Ala1186Gly) | |
| 7 | g.128845022C>T | CA369197234 | FLNC | c.3557C>T (p.Ala1186Val) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.128845023G>A | CA4475068 | FLNC | c.3558G>A (p.Ala1186=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.128845023G>C | CA457848433 | FLNC | c.3558G>C (p.Ala1186=) | |
| 7 | g.128845023G= | CA1742584820 | FLNC | c.3558G= (p.Ala1186=) | |
| 7 | g.128845023G>T | CA457848431 | FLNC | c.3558G>T (p.Ala1186=) | dbSNP |
| 7 | g.128845024G>A | CA369197236 | FLNC | c.3559G>A (p.Glu1187Lys) | COSMIC |
| 7 | g.128845024G>C | CA369197237 | FLNC | c.3559G>C (p.Glu1187Gln) | |
| 7 | g.128845024G>T | CA369197238 | FLNC | c.3559G>T (p.Glu1187Ter) | |
| 7 | g.128845025A>C | CA369197239 | FLNC | c.3560A>C (p.Glu1187Ala) | |
| 7 | g.128845025A>G | CA369197241 | FLNC | c.3560A>G (p.Glu1187Gly) | |
| 7 | g.128845025A>T | CA369197240 | FLNC | c.3560A>T (p.Glu1187Val) |