Primary Site >> Stomach Cancer
Gene >> MVK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228510 |
| Start | 109579880:109579880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.305C>A |
| AA Mutation | p.Ala102Asp(p.A102D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228510 |
| Start | 109590806:109590806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.713A>C |
| AA Mutation | p.Lys238Thr(p.K238T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228510 |
| Start | 109595116:109595116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374686559 |
| CDS Mutation | c.974G>A |
| AA Mutation | p.Arg325His(p.R325H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228510 |
| Start | 109586081:109586081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.587T>A |
| AA Mutation | p.Ile196Asn(p.I196N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228510 |
| Start | 109581406:109581406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.383G>A |
| AA Mutation | p.Ser128Asn(p.S128N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228510 |
| Start | 109581464:109581464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138342076 |
| CDS Mutation | c.441C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |