Primary Site >> Stomach Cancer
Gene >> SLC16A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369626 |
| Start | 112914159:112914159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1235T>A |
| AA Mutation | p.Leu412His(p.L412H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369626 |
| Start | 112917405:112917405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763573918 |
| CDS Mutation | c.1001C>T |
| AA Mutation | p.Ala334Val(p.A334V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369626 |
| Start | 112914072:112914072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1322T>C |
| AA Mutation | p.Met441Thr(p.M441T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369626 |
| Start | 112922072:112922072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.279C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369626 |
| Start | 112922027:112922027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147057122 |
| CDS Mutation | c.324C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369626 |
| Start | 112929268:112929268(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.41delC |
| AA Mutation | p.Pro14GlnfsTer10(p.P14Qfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000369626 |
| Start | 112917424:112917424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs606231310 |
| CDS Mutation | c.982C>T |
| AA Mutation | p.Arg328Ter(p.R328*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369626 |
| Start | 112929267:112929268(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs606231309 |
| CDS Mutation | c.41dupC |
| AA Mutation | p.Asp15ArgfsTer34(p.D15Rfs*34) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |