Primary Site >> Stomach Cancer
Gene >> FLNB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58123432:58123432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771189591 |
| CDS Mutation | c.3466G>A |
| AA Mutation | p.Val1156Ile(p.V1156I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58138308:58138308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4888A>T |
| AA Mutation | p.Thr1630Ser(p.T1630S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58148792:58148792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781212517 |
| CDS Mutation | c.6031G>A |
| AA Mutation | p.Gly2011Ser(p.G2011S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58104009:58104009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201544295 |
| CDS Mutation | c.1534G>A |
| AA Mutation | p.Ala512Thr(p.A512T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58156049:58156049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765247131 |
| CDS Mutation | c.6862C>T |
| AA Mutation | p.Arg2288Cys(p.R2288C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58153473:58153473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6466C>T |
| AA Mutation | p.Arg2156Trp(p.R2156W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58148678:58148678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368965386 |
| CDS Mutation | c.5917G>A |
| AA Mutation | p.Glu1973Lys(p.E1973K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58149984:58149984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141559684 |
| CDS Mutation | c.6226G>A |
| AA Mutation | p.Ala2076Thr(p.A2076T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58097963:58097963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1133A>G |
| AA Mutation | p.Asp378Gly(p.D378G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58125677:58125677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3995A>T |
| AA Mutation | p.Gln1332Leu(p.Q1332L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58111830:58111830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2524T>C |
| AA Mutation | p.Ser842Pro(p.S842P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58156047:58156047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6860C>T |
| AA Mutation | p.Ala2287Val(p.A2287V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58121478:58121478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3101C>A |
| AA Mutation | p.Ala1034Asp(p.A1034D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58138485:58138485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762205881 |
| CDS Mutation | c.5065C>T |
| AA Mutation | p.Arg1689Cys(p.R1689C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58159638:58159638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6973A>G |
| AA Mutation | p.Ser2325Gly(p.S2325G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58136121:58136121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201630300 |
| CDS Mutation | c.4814G>A |
| AA Mutation | p.Arg1605His(p.R1605H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58163163:58163163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7031C>A |
| AA Mutation | p.Ala2344Asp(p.A2344D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58112233:58112233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753985242 |
| CDS Mutation | c.2660C>T |
| AA Mutation | p.Pro887Leu(p.P887L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58154841:58154841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754754415 |
| CDS Mutation | c.6685G>A |
| AA Mutation | p.Ala2229Thr(p.A2229T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58156031:58156031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6844G>A |
| AA Mutation | p.Ala2282Thr(p.A2282T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58008604:58008604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.40T>C |
| AA Mutation | p.Trp14Arg(p.W14R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58112310:58112310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2737A>G |
| AA Mutation | p.Thr913Ala(p.T913A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295956 |
| Start | 58124352:58124352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3745A>G |
| AA Mutation | p.Thr1249Ala(p.T1249A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295956 |
| Start | 58126635:58126635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4095T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295956 |
| Start | 58169621:58169621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201257749 |
| CDS Mutation | c.7449C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295956 |
| Start | 58153496:58153496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746887183 |
| CDS Mutation | c.6489C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295956 |
| Start | 58136089:58136089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779187199 |
| CDS Mutation | c.4782C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295956 |
| Start | 58118901:58118901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2775T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295956 |
| Start | 58078748:58078748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777288549 |
| CDS Mutation | c.573G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295956 |
| Start | 58094867:58094867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.819G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295956 |
| Start | 58146027:58146027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202240037 |
| CDS Mutation | c.5532C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000295956 |
| Start | 58104061:58104061(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs758401425 |
| CDS Mutation | c.1592delG |
| AA Mutation | p.Gly531AspfsTer42(p.G531Dfs*42) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000295956 |
| Start | 58170713:58170713(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.7765delG |
| AA Mutation | p.Glu2589ArgfsTer48(p.E2589Rfs*48) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000295956 |
| Start | 58008635:58008647(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.73_85delTGGTGCAACGAGC |
| AA Mutation | p.Trp25ThrfsTer5(p.W25Tfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000295956 |
| Start | 58146046:58146046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5551G>T |
| AA Mutation | p.Glu1851Ter(p.E1851*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000295956 |
| Start | 58108461:58108461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs80356517 |
| CDS Mutation | c.1945C>T |
| AA Mutation | p.Arg649Ter(p.R649*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000295956 |
| Start | 58123572:58123572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3606C>G |
| AA Mutation | p.Tyr1202Ter(p.Y1202*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000295956 |
| Start | 58148319:58148319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5842C>T |
| AA Mutation | p.Arg1948Ter(p.R1948*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000295956 |
| Start | 58104060:58104061(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs746105983 |
| CDS Mutation | c.1592dupG |
| AA Mutation | p.His532ThrfsTer9(p.H532Tfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000295956 |
| Start | 58081720:58081721(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.736dupG |
| AA Mutation | p.Ala246GlyfsTer49(p.A246Gfs*49) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000295956 |
| Start | 58132847:58132848(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.4439_4440dupCA |
| AA Mutation | p.Val1481GlnfsTer2(p.V1481Qfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000295956 |
| Start | 58125745:58125745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4061+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |