Primary Site >> Stomach Cancer
Gene >> FLNC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128853804:128853804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6451G>A |
| AA Mutation | p.Gly2151Ser(p.G2151S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128844845:128844845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3380G>A |
| AA Mutation | p.Gly1127Asp(p.G1127D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128846053:128846053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3854G>A |
| AA Mutation | p.Gly1285Asp(p.G1285D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128845148:128845148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3683T>C |
| AA Mutation | p.Ile1228Thr(p.I1228T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128854662:128854662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201028676 |
| CDS Mutation | c.6977G>A |
| AA Mutation | p.Arg2326Gln(p.R2326Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128846758:128846758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766513255 |
| CDS Mutation | c.4141G>A |
| AA Mutation | p.Gly1381Arg(p.G1381R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128835535:128835535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.562G>A |
| AA Mutation | p.Gly188Ser(p.G188S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128844976:128844976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769490872 |
| CDS Mutation | c.3511G>A |
| AA Mutation | p.Gly1171Ser(p.G1171S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128848064:128848064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746275035 |
| CDS Mutation | c.4576C>T |
| AA Mutation | p.Arg1526Cys(p.R1526C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128848679:128848679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369842920 |
| CDS Mutation | c.4699C>T |
| AA Mutation | p.Arg1567Trp(p.R1567W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128854096:128854096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758838323 |
| CDS Mutation | c.6607C>T |
| AA Mutation | p.Arg2203Cys(p.R2203C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128830842:128830842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758342140 |
| CDS Mutation | c.205C>T |
| AA Mutation | p.Arg69Trp(p.R69W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128846445:128846445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761881020 |
| CDS Mutation | c.4109G>A |
| AA Mutation | p.Arg1370Gln(p.R1370Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128843808:128843808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2824G>A |
| AA Mutation | p.Val942Met(p.V942M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128830795:128830795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.158T>C |
| AA Mutation | p.Val53Ala(p.V53A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128835452:128835452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.479C>T |
| AA Mutation | p.Thr160Met(p.T160M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128857134:128857134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7578C>A |
| AA Mutation | p.Phe2526Leu(p.F2526L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128844079:128844079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202039743 |
| CDS Mutation | c.3005G>A |
| AA Mutation | p.Arg1002Gln(p.R1002Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128854052:128854052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769574342 |
| CDS Mutation | c.6563C>T |
| AA Mutation | p.Thr2188Met(p.T2188M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128837700:128837700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.914C>T |
| AA Mutation | p.Ala305Val(p.A305V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128835361:128835361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.388A>G |
| AA Mutation | p.Ile130Val(p.I130V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128830849:128830849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.212T>C |
| AA Mutation | p.Ile71Thr(p.I71T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128854502:128854502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372251350 |
| CDS Mutation | c.6817G>A |
| AA Mutation | p.Ala2273Thr(p.A2273T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128838696:128838696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199935488 |
| CDS Mutation | c.1304C>T |
| AA Mutation | p.Thr435Met(p.T435M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128852692:128852692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538779271 |
| CDS Mutation | c.5944C>T |
| AA Mutation | p.Arg1982Cys(p.R1982C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128856594:128856594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370293647 |
| CDS Mutation | c.7328G>A |
| AA Mutation | p.Arg2443Gln(p.R2443Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128853022:128853022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754160175 |
| CDS Mutation | c.6199C>G |
| AA Mutation | p.Arg2067Gly(p.R2067G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128842895:128842895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746478952 |
| CDS Mutation | c.2491G>A |
| AA Mutation | p.Val831Ile(p.V831I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128845144:128845144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3679A>G |
| AA Mutation | p.Thr1227Ala(p.T1227A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128844887:128844887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3422C>A |
| AA Mutation | p.Pro1141His(p.P1141H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128853472:128853472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6212A>G |
| AA Mutation | p.Tyr2071Cys(p.Y2071C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128846110:128846110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377011299 |
| CDS Mutation | c.3911T>C |
| AA Mutation | p.Val1304Ala(p.V1304A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128835440:128835440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.467C>T |
| AA Mutation | p.Ala156Val(p.A156V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128849370:128849370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780829334 |
| CDS Mutation | c.4991C>T |
| AA Mutation | p.Thr1664Met(p.T1664M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128830903:128830903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.266G>A |
| AA Mutation | p.Arg89His(p.R89H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128854166:128854166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6677T>C |
| AA Mutation | p.Leu2226Pro(p.L2226P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128842883:128842883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2479G>A |
| AA Mutation | p.Asp827Asn(p.D827N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128830682:128830682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.45C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128847845:128847845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4437G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128858481:128858481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748104907 |
| CDS Mutation | c.8136C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128850873:128850873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550620019 |
| CDS Mutation | c.5469G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128848690:128848690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774692750 |
| CDS Mutation | c.4710C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128854501:128854501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375139827 |
| CDS Mutation | c.6816C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128835567:128835567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375617228 |
| CDS Mutation | c.594C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128855257:128855257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7194G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128857167:128857167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7611C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128846895:128846895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4278G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128858394:128858394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs183104951 |
| CDS Mutation | c.8049C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128856782:128856782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755019331 |
| CDS Mutation | c.7422C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128830823:128830823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.186C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128846365:128846365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767426611 |
| CDS Mutation | c.4029C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128852640:128852640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747546440 |
| CDS Mutation | c.5892C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128843457:128843457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758116420 |
| CDS Mutation | c.2691C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000325888 |
| Start | 128838762:128838762(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1374delC |
| AA Mutation | p.Ile459SerfsTer33(p.I459Sfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000325888 |
| Start | 128841337:128841337(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1981delG |
| AA Mutation | p.Ala661ProfsTer10(p.A661Pfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000325888 |
| Start | 128840064:128840064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1453C>T |
| AA Mutation | p.Gln485Ter(p.Q485*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000325888 |
| Start | 128842375:128842375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2265+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |