Primary Site >> Stomach Cancer
Gene >> IL7R
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303115 |
| Start | 35860900:35860900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.131G>T |
| AA Mutation | p.Ser44Ile(p.S44I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303115 |
| Start | 35876241:35876241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200570812 |
| CDS Mutation | c.1135G>A |
| AA Mutation | p.Ala379Thr(p.A379T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303115 |
| Start | 35876454:35876454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1348G>A |
| AA Mutation | p.Val450Ile(p.V450I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303115 |
| Start | 35860888:35860888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.119T>C |
| AA Mutation | p.Phe40Ser(p.F40S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303115 |
| Start | 35857043:35857043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.66T>A |
| AA Mutation | p.Ser22Arg(p.S22R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303115 |
| Start | 35876323:35876323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1217T>G |
| AA Mutation | p.Leu406Arg(p.L406R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303115 |
| Start | 35876290:35876290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1184A>C |
| AA Mutation | p.Lys395Thr(p.K395T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000303115 |
| Start | 35874535:35874535(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.799delA |
| AA Mutation | p.Arg267GlyfsTer28(p.R267Gfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000303115 |
| Start | 35867439:35867439(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.361delA |
| AA Mutation | p.Ile121Ter(p.I121*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000303115 |
| Start | 35873558:35873558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201559094 |
| CDS Mutation | c.616C>T |
| AA Mutation | p.Arg206Ter(p.R206*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000303115 |
| Start | 35867438:35867439(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs781000678 |
| CDS Mutation | c.361dupA |
| AA Mutation | p.Ile121AsnfsTer8(p.I121Nfs*8) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000303115 |
| Start | 35874534:35874535(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.799dupA |
| AA Mutation | p.Arg267LysfsTer3(p.R267Kfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |