Primary Site >> Stomach Cancer
Gene >> TNFRSF9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377507 |
| Start | 7920856:7920856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.747A>C |
| AA Mutation | p.Glu249Asp(p.E249D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377507 |
| Start | 7937702:7937702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186372948 |
| CDS Mutation | c.401G>A |
| AA Mutation | p.Arg134Gln(p.R134Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377507 |
| Start | 7935105:7935105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769884031 |
| CDS Mutation | c.452C>T |
| AA Mutation | p.Thr151Met(p.T151M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377507 |
| Start | 7933198:7933198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143524950 |
| CDS Mutation | c.643C>T |
| AA Mutation | p.Arg215Trp(p.R215W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377507 |
| Start | 7938804:7938804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.125A>C |
| AA Mutation | p.Asn42Thr(p.N42T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377507 |
| Start | 7935057:7935057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145966863 |
| CDS Mutation | c.500C>T |
| AA Mutation | p.Pro167Leu(p.P167L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377507 |
| Start | 7933248:7933248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748890197 |
| CDS Mutation | c.593C>T |
| AA Mutation | p.Ala198Val(p.A198V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377507 |
| Start | 7933247:7933247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143532137 |
| CDS Mutation | c.594G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000377507 |
| Start | 7938194:7938194(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs752649731 |
| CDS Mutation | c.345delA |
| AA Mutation | p.Gly116ValfsTer33(p.G116Vfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |