Primary Site >> Stomach Cancer
Gene >> FDPS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356657 |
| Start | 155317978:155317978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.518A>C |
| AA Mutation | p.Asp173Ala(p.D173A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356657 |
| Start | 155320592:155320592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1243T>C |
| AA Mutation | p.Tyr415His(p.Y415H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356657 |
| Start | 155312364:155312364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373639609 |
| CDS Mutation | c.449G>A |
| AA Mutation | p.Arg150Gln(p.R150Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356657 |
| Start | 155318277:155318277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139546057 |
| CDS Mutation | c.670G>A |
| AA Mutation | p.Glu224Lys(p.E224K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356657 |
| Start | 155320541:155320541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1192T>C |
| AA Mutation | p.Tyr398His(p.Y398H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356657 |
| Start | 155319821:155319821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.952C>T |
| AA Mutation | p.Pro318Ser(p.P318S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356657 |
| Start | 155318175:155318175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757544890 |
| CDS Mutation | c.568G>A |
| AA Mutation | p.Val190Met(p.V190M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356657 |
| Start | 155320582:155320582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779964878 |
| CDS Mutation | c.1233G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000356657 |
| Start | 155318711:155318711(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.736delC |
| AA Mutation | p.Gln246ArgfsTer31(p.Q246Rfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000356657 |
| Start | 155318710:155318711(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.735_736dupCC |
| AA Mutation | p.Gln246ProfsTer32(p.Q246Pfs*32) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |