Primary Site >> Stomach Cancer
Gene >> GRK6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355472 |
| Start | 177441758:177441758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748162611 |
| CDS Mutation | c.1699G>A |
| AA Mutation | p.Asp567Asn(p.D567N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355472 |
| Start | 177433643:177433643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.705G>T |
| AA Mutation | p.Lys235Asn(p.K235N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000355472 |
| Start | 177431997:177431997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.151C>T |
| AA Mutation | p.Arg51Cys(p.R51C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355472 |
| Start | 177434092:177434092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780128630 |
| CDS Mutation | c.917G>A |
| AA Mutation | p.Arg306His(p.R306H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355472 |
| Start | 177433177:177433177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.471T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355472 |
| Start | 177432780:177432780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.414C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355472 |
| Start | 177436242:177436242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774743489 |
| CDS Mutation | c.1227C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355472 |
| Start | 177440834:177440834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375413182 |
| CDS Mutation | c.1539C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355472 |
| Start | 177434920:177434920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.948C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |