Primary Site >> Stomach Cancer
Gene >> TM4SF5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270560 |
| Start | 4782870:4782870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.412A>G |
| AA Mutation | p.Asn138Asp(p.N138D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270560 |
| Start | 4782599:4782599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.355T>G |
| AA Mutation | p.Leu119Val(p.L119V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000270560 |
| Start | 4782514:4782514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.270G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000270560 |
| Start | 4782529:4782529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.285G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000270560 |
| Start | 4782995:4782995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763826018 |
| CDS Mutation | c.537C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000270560 |
| Start | 4782893:4782893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.435C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000270560 |
| Start | 4782900:4782900(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.446delC |
| AA Mutation | p.Pro149LeufsTer8(p.P149Lfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | start_lost |
| Transcription ID | ENST00000270560 |
| Start | 4771923:4771923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768321534 |
| CDS Mutation | c.1A>T |
| AA Mutation | p.Met1?(p.M1?) |
| Mutation Classification | Translation_Start_Site |
| Feature Type | Transcript |