Primary Site >> Stomach Cancer
Gene >> VTN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226218 |
| Start | 28369013:28369013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782409757 |
| CDS Mutation | c.685C>T |
| AA Mutation | p.Arg229Cys(p.R229C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226218 |
| Start | 28369521:28369521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.515T>G |
| AA Mutation | p.Leu172Arg(p.L172R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226218 |
| Start | 28369012:28369012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782268632 |
| CDS Mutation | c.686G>A |
| AA Mutation | p.Arg229His(p.R229H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226218 |
| Start | 28367810:28367810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1229G>A |
| AA Mutation | p.Ser410Asn(p.S410N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226218 |
| Start | 28369824:28369824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201384220 |
| CDS Mutation | c.212C>T |
| AA Mutation | p.Pro71Leu(p.P71L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226218 |
| Start | 28368905:28368905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.793T>C |
| AA Mutation | p.Tyr265His(p.Y265H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226218 |
| Start | 28370194:28370194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10C>A |
| AA Mutation | p.Leu4Met(p.L4M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226218 |
| Start | 28368548:28368548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782190887 |
| CDS Mutation | c.952G>A |
| AA Mutation | p.Glu318Lys(p.E318K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226218 |
| Start | 28369665:28369665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144093348 |
| CDS Mutation | c.371C>T |
| AA Mutation | p.Ala124Val(p.A124V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226218 |
| Start | 28370177:28370177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.27A>G |
| AA Mutation | p.Ile9Met(p.I9M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000226218 |
| Start | 28367848:28367848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1191C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000226218 |
| Start | 28368939:28368939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782405279 |
| CDS Mutation | c.759C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |