Primary Site >> Stomach Cancer
Gene >> PC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66850393:66850393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2545G>A |
| AA Mutation | p.Asp849Asn(p.D849N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66871701:66871701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.307A>G |
| AA Mutation | p.Ile103Val(p.I103V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66871327:66871327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768981875 |
| CDS Mutation | c.475G>A |
| AA Mutation | p.Ala159Thr(p.A159T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66850112:66850112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs796052032 |
| CDS Mutation | c.2723C>T |
| AA Mutation | p.Thr908Met(p.T908M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66850877:66850877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2270G>T |
| AA Mutation | p.Ser757Ile(p.S757I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000393955 |
| Start | 66852834:66852834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1516C>A |
| AA Mutation | p.His506Asn(p.H506N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66852516:66852516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs119103242 |
| CDS Mutation | c.1748G>A |
| AA Mutation | p.Arg583His(p.R583H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66871353:66871353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.449G>T |
| AA Mutation | p.Gly150Val(p.G150V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66849750:66849750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145046106 |
| CDS Mutation | c.3008C>T |
| AA Mutation | p.Thr1003Met(p.T1003M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66871838:66871838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780682688 |
| CDS Mutation | c.170C>T |
| AA Mutation | p.Thr57Met(p.T57M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66849334:66849334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3184G>A |
| AA Mutation | p.Ala1062Thr(p.A1062T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66850055:66850055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2780G>A |
| AA Mutation | p.Ser927Asn(p.S927N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66866242:66866242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1130G>A |
| AA Mutation | p.Arg377Gln(p.R377Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66849697:66849697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3061A>G |
| AA Mutation | p.Lys1021Glu(p.K1021E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66866270:66866270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764979642 |
| CDS Mutation | c.1102C>T |
| AA Mutation | p.Arg368Cys(p.R368C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66850868:66850868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543756586 |
| CDS Mutation | c.2279G>A |
| AA Mutation | p.Arg760Gln(p.R760Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66849248:66849248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3270G>T |
| AA Mutation | p.Lys1090Asn(p.K1090N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393955 |
| Start | 66850045:66850045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2790G>T |
| AA Mutation | p.Glu930Asp(p.E930D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393955 |
| Start | 66850810:66850810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377708277 |
| CDS Mutation | c.2337C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393955 |
| Start | 66852533:66852533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1731G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393955 |
| Start | 66850403:66850403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534635326 |
| CDS Mutation | c.2535C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393955 |
| Start | 66851142:66851142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2121G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393955 |
| Start | 66871142:66871142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139717038 |
| CDS Mutation | c.543C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000393955 |
| Start | 66849961:66849961(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2874delG |
| AA Mutation | p.Phe959SerfsTer10(p.F959Sfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000393955 |
| Start | 66851069:66851069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2194C>T |
| AA Mutation | p.Arg732Ter(p.R732*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |