Primary Site >> Stomach Cancer
Gene >> CENPF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214644675:214644675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5105T>A |
| AA Mutation | p.Leu1702His(p.L1702H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214618668:214618668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.455C>T |
| AA Mutation | p.Pro152Leu(p.P152L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214645950:214645950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6380G>A |
| AA Mutation | p.Arg2127His(p.R2127H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214642096:214642096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3758T>C |
| AA Mutation | p.Met1253Thr(p.M1253T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214645608:214645608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150986314 |
| CDS Mutation | c.6038C>T |
| AA Mutation | p.Thr2013Met(p.T2013M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214620842:214620842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.761C>A |
| AA Mutation | p.Pro254Gln(p.P254Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214657099:214657099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8652A>T |
| AA Mutation | p.Gln2884His(p.Q2884H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214645961:214645961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181293702 |
| CDS Mutation | c.6391G>A |
| AA Mutation | p.Asp2131Asn(p.D2131N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214642489:214642489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4151T>C |
| AA Mutation | p.Leu1384Ser(p.L1384S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214622191:214622191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.978A>T |
| AA Mutation | p.Lys326Asn(p.K326N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214642966:214642966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141012292 |
| CDS Mutation | c.4628C>T |
| AA Mutation | p.Ser1543Leu(p.S1543L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214640759:214640759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2421G>T |
| AA Mutation | p.Met807Ile(p.M807I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214620848:214620848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147545168 |
| CDS Mutation | c.767G>A |
| AA Mutation | p.Arg256Gln(p.R256Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214629063:214629063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1086A>C |
| AA Mutation | p.Gln362His(p.Q362H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214640631:214640631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2293G>A |
| AA Mutation | p.Asp765Asn(p.D765N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214642565:214642565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4227G>T |
| AA Mutation | p.Glu1409Asp(p.E1409D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214642940:214642940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4602G>T |
| AA Mutation | p.Glu1534Asp(p.E1534D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214652858:214652858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8191A>G |
| AA Mutation | p.Lys2731Glu(p.K2731E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214640497:214640497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2159A>T |
| AA Mutation | p.Asn720Ile(p.N720I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214630621:214630621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1282G>T |
| AA Mutation | p.Ala428Ser(p.A428S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214642930:214642930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4592T>C |
| AA Mutation | p.Leu1531Pro(p.L1531P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214640482:214640482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2144A>G |
| AA Mutation | p.Gln715Arg(p.Q715R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214645704:214645704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6134A>G |
| AA Mutation | p.Gln2045Arg(p.Q2045R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214646093:214646093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6523C>A |
| AA Mutation | p.Leu2175Ile(p.L2175I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214642474:214642474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4136T>G |
| AA Mutation | p.Val1379Gly(p.V1379G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214645581:214645581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6011T>C |
| AA Mutation | p.Val2004Ala(p.V2004A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214652906:214652906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8239G>T |
| AA Mutation | p.Asp2747Tyr(p.D2747Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214645705:214645705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6135G>T |
| AA Mutation | p.Gln2045His(p.Q2045H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214646521:214646521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6951G>T |
| AA Mutation | p.Gln2317His(p.Q2317H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366955 |
| Start | 214647379:214647379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7809C>A |
| AA Mutation | p.Asp2603Glu(p.D2603E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366955 |
| Start | 214620936:214620936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114104425 |
| CDS Mutation | c.855G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366955 |
| Start | 214646026:214646026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559968112 |
| CDS Mutation | c.6456T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366955 |
| Start | 214640525:214640525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2187T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366955 |
| Start | 214641425:214641425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3087T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366955 |
| Start | 214642490:214642490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4152G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366955 |
| Start | 214645291:214645291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5721C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366955 |
| Start | 214656937:214656937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8490T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366955 |
| Start | 214642391:214642391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4053T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366955 |
| Start | 214642670:214642670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372343987 |
| CDS Mutation | c.4332C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366955 |
| Start | 214658866:214658866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8979G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366955 |
| Start | 214645483:214645483(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.5920delA |
| AA Mutation | p.Thr1974ProfsTer11(p.T1974Pfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366955 |
| Start | 214657310:214657310(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.8869delA |
| AA Mutation | p.Ser2957AlafsTer6(p.S2957Afs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000366955 |
| Start | 214642922:214642922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4584C>A |
| AA Mutation | p.Cys1528Ter(p.C1528*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000366955 |
| Start | 214619179:214619179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199800194 |
| CDS Mutation | c.532C>T |
| AA Mutation | p.Arg178Ter(p.R178*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366955 |
| Start | 214618655:214618656(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.447dupT |
| AA Mutation | p.Thr150TyrfsTer11(p.T150Yfs*11) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |