Primary Site >> Stomach Cancer
Gene >> TMPRSS13
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524993 |
| Start | 117908683:117908683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1211G>A |
| AA Mutation | p.Ser404Asn(p.S404N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524993 |
| Start | 117918478:117918478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752289870 |
| CDS Mutation | c.382G>A |
| AA Mutation | p.Gly128Arg(p.G128R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524993 |
| Start | 117909927:117909927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.988G>A |
| AA Mutation | p.Ala330Thr(p.A330T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524993 |
| Start | 117909936:117909936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778644730 |
| CDS Mutation | c.979G>A |
| AA Mutation | p.Val327Met(p.V327M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524993 |
| Start | 117917224:117917224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200625070 |
| CDS Mutation | c.502C>T |
| AA Mutation | p.Leu168Phe(p.L168F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524993 |
| Start | 117918502:117918502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.358T>C |
| AA Mutation | p.Tyr120His(p.Y120H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524993 |
| Start | 117908779:117908779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1115G>T |
| AA Mutation | p.Arg372Leu(p.R372L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000524993 |
| Start | 117918749:117918749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.111C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000524993 |
| Start | 117917213:117917213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367945751 |
| CDS Mutation | c.513C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |