Primary Site >> Stomach Cancer
Gene >> CCKAR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295589 |
| Start | 26481719:26481719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1206G>T |
| AA Mutation | p.Glu402Asp(p.E402D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295589 |
| Start | 26481912:26481912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1013A>G |
| AA Mutation | p.Tyr338Cys(p.Y338C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295589 |
| Start | 26485871:26485871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.392A>T |
| AA Mutation | p.Asn131Ile(p.N131I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295589 |
| Start | 26481706:26481706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751151975 |
| CDS Mutation | c.1219G>A |
| AA Mutation | p.Gly407Arg(p.G407R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295589 |
| Start | 26489469:26489469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.128T>C |
| AA Mutation | p.Val43Ala(p.V43A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295589 |
| Start | 26485872:26485872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.391A>G |
| AA Mutation | p.Asn131Asp(p.N131D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295589 |
| Start | 26481938:26481938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.987C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295589 |
| Start | 26481926:26481926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199510290 |
| CDS Mutation | c.999C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295589 |
| Start | 26485825:26485825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.438C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295589 |
| Start | 26482127:26482127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.798C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295589 |
| Start | 26481674:26481674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs79677636 |
| CDS Mutation | c.1251G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |