Primary Site >> Stomach Cancer
Gene >> P2RY6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349767 |
| Start | 73296888:73296888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370867718 |
| CDS Mutation | c.370C>T |
| AA Mutation | p.Arg124Cys(p.R124C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349767 |
| Start | 73297170:73297170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141420011 |
| CDS Mutation | c.652C>T |
| AA Mutation | p.Arg218Cys(p.R218C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349767 |
| Start | 73297321:73297321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139384226 |
| CDS Mutation | c.803C>T |
| AA Mutation | p.Thr268Met(p.T268M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349767 |
| Start | 73296579:73296579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754852770 |
| CDS Mutation | c.61C>T |
| AA Mutation | p.Arg21Cys(p.R21C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349767 |
| Start | 73297039:73297039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780427456 |
| CDS Mutation | c.521G>A |
| AA Mutation | p.Arg174His(p.R174H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349767 |
| Start | 73296969:73296969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374484031 |
| CDS Mutation | c.451G>A |
| AA Mutation | p.Val151Met(p.V151M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349767 |
| Start | 73296939:73296939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757708551 |
| CDS Mutation | c.421C>T |
| AA Mutation | p.Arg141Cys(p.R141C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349767 |
| Start | 73297501:73297501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs193163379 |
| CDS Mutation | c.983G>T |
| AA Mutation | p.Arg328Leu(p.R328L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349767 |
| Start | 73296582:73296582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61745521 |
| CDS Mutation | c.64G>A |
| AA Mutation | p.Glu22Lys(p.E22K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349767 |
| Start | 73297400:73297400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542361416 |
| CDS Mutation | c.882C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000349767 |
| Start | 73297041:73297042(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.524_525dupCT |
| AA Mutation | p.Val176LeufsTer184(p.V176Lfs*184) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |