Primary Site >> Stomach Cancer
Gene >> AATK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326724 |
| Start | 81121307:81121307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780911896 |
| CDS Mutation | c.2629G>A |
| AA Mutation | p.Asp877Asn(p.D877N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326724 |
| Start | 81121978:81121978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762845072 |
| CDS Mutation | c.1958C>T |
| AA Mutation | p.Ala653Val(p.A653V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326724 |
| Start | 81120323:81120323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs572926712 |
| CDS Mutation | c.3613C>T |
| AA Mutation | p.Arg1205Cys(p.R1205C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326724 |
| Start | 81122723:81122723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1213G>A |
| AA Mutation | p.Glu405Lys(p.E405K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326724 |
| Start | 81120322:81120322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184348609 |
| CDS Mutation | c.3614G>A |
| AA Mutation | p.Arg1205His(p.R1205H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326724 |
| Start | 81121004:81121004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368177200 |
| CDS Mutation | c.2932C>T |
| AA Mutation | p.Arg978Trp(p.R978W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326724 |
| Start | 81121265:81121265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184717207 |
| CDS Mutation | c.2671C>T |
| AA Mutation | p.Arg891Cys(p.R891C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326724 |
| Start | 81121929:81121929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2007G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326724 |
| Start | 81121956:81121956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs55881512 |
| CDS Mutation | c.1980C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326724 |
| Start | 81120324:81120324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3612G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326724 |
| Start | 81134431:81134431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.126C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326724 |
| Start | 81134377:81134377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745405011 |
| CDS Mutation | c.180C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326724 |
| Start | 81121689:81121689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2247C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326724 |
| Start | 81120432:81120432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3504C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326724 |
| Start | 81121815:81121815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538497193 |
| CDS Mutation | c.2121C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326724 |
| Start | 81119570:81119570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548952463 |
| CDS Mutation | c.3894C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326724 |
| Start | 81134437:81134437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548878853 |
| CDS Mutation | c.120C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |