Primary Site >> Stomach Cancer
Gene >> TNPO1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337273 |
| Start | 72887084:72887084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1165G>A |
| AA Mutation | p.Ala389Thr(p.A389T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337273 |
| Start | 72872647:72872647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.605C>T |
| AA Mutation | p.Ala202Val(p.A202V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337273 |
| Start | 72877280:72877280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.854G>A |
| AA Mutation | p.Cys285Tyr(p.C285Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337273 |
| Start | 72888161:72888161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1387C>T |
| AA Mutation | p.Arg463Cys(p.R463C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337273 |
| Start | 72861840:72861840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.388G>C |
| AA Mutation | p.Glu130Gln(p.E130Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337273 |
| Start | 72872680:72872680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.638G>A |
| AA Mutation | p.Arg213Lys(p.R213K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000337273 |
| Start | 72875736:72875736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.800A>C |
| AA Mutation | p.Glu267Ala(p.E267A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337273 |
| Start | 72883131:72883131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777038547 |
| CDS Mutation | c.1049C>T |
| AA Mutation | p.Ser350Leu(p.S350L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337273 |
| Start | 72905332:72905332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757982142 |
| CDS Mutation | c.2619C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |