Primary Site >> Stomach Cancer
Gene >> TNFRSF1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162749 |
| Start | 6329530:6329530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1150G>A |
| AA Mutation | p.Glu384Lys(p.E384K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162749 |
| Start | 6329466:6329466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1214C>T |
| AA Mutation | p.Ala405Val(p.A405V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162749 |
| Start | 6333091:6333091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.529A>G |
| AA Mutation | p.Asn177Asp(p.N177D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162749 |
| Start | 6329571:6329571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1109G>A |
| AA Mutation | p.Arg370His(p.R370H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162749 |
| Start | 6329361:6329361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1319C>T |
| AA Mutation | p.Ala440Val(p.A440V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000162749 |
| Start | 6330665:6330665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202150552 |
| CDS Mutation | c.672T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000162749 |
| Start | 6330282:6330282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201358363 |
| CDS Mutation | c.753G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000162749 |
| Start | 6330902:6330902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779458638 |
| CDS Mutation | c.576G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |