Primary Site >> Stomach Cancer
Gene >> ATP2A3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352011 |
| Start | 3951317:3951317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.397G>T |
| AA Mutation | p.Asp133Tyr(p.D133Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352011 |
| Start | 3936301:3936301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2490T>G |
| AA Mutation | p.Ser830Arg(p.S830R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352011 |
| Start | 3947398:3947398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1088T>C |
| AA Mutation | p.Val363Ala(p.V363A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352011 |
| Start | 3947734:3947734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144288676 |
| CDS Mutation | c.752G>A |
| AA Mutation | p.Arg251His(p.R251H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352011 |
| Start | 3942713:3942713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1438C>T |
| AA Mutation | p.Arg480Trp(p.R480W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352011 |
| Start | 3951386:3951386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199903488 |
| CDS Mutation | c.328C>T |
| AA Mutation | p.Arg110Cys(p.R110C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352011 |
| Start | 3936317:3936317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373288442 |
| CDS Mutation | c.2474G>A |
| AA Mutation | p.Arg825Gln(p.R825Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352011 |
| Start | 3930350:3930350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2695A>G |
| AA Mutation | p.Met899Val(p.M899V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352011 |
| Start | 3951381:3951381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774597476 |
| CDS Mutation | c.333C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352011 |
| Start | 3947421:3947421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757618073 |
| CDS Mutation | c.1065G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352011 |
| Start | 3947550:3947550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374049814 |
| CDS Mutation | c.936G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352011 |
| Start | 3941043:3941043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748606666 |
| CDS Mutation | c.2028C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352011 |
| Start | 3941283:3941283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201719837 |
| CDS Mutation | c.1788C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352011 |
| Start | 3947811:3947811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.675C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352011 |
| Start | 3941082:3941082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201705121 |
| CDS Mutation | c.1989C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352011 |
| Start | 3947475:3947475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770562560 |
| CDS Mutation | c.1011G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000352011 |
| Start | 3942624:3942625(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1526dupG |
| AA Mutation | p.Ser510GlnfsTer10(p.S510Qfs*10) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |