Primary Site >> Stomach Cancer
Gene >> AQP8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219660 |
| Start | 25227118:25227118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762948461 |
| CDS Mutation | c.653C>T |
| AA Mutation | p.Ala218Val(p.A218V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219660 |
| Start | 25217282:25217282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557244284 |
| CDS Mutation | c.97C>T |
| AA Mutation | p.Arg33Trp(p.R33W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000219660 |
| Start | 25221459:25221459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.263G>C |
| AA Mutation | p.Gly88Ala(p.G88A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219660 |
| Start | 25217340:25217340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.155G>A |
| AA Mutation | p.Gly52Glu(p.G52E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219660 |
| Start | 25227127:25227127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.662C>A |
| AA Mutation | p.Ala221Asp(p.A221D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219660 |
| Start | 25217436:25217436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.251G>A |
| AA Mutation | p.Gly84Glu(p.G84E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219660 |
| Start | 25217343:25217343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.158G>T |
| AA Mutation | p.Cys53Phe(p.C53F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219660 |
| Start | 25217367:25217367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111572783 |
| CDS Mutation | c.182C>T |
| AA Mutation | p.Thr61Met(p.T61M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219660 |
| Start | 25217290:25217290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138426074 |
| CDS Mutation | c.105G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000219660 |
| Start | 25221554:25221554(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs759782104 |
| CDS Mutation | c.363delG |
| AA Mutation | p.Met122CysfsTer10(p.M122Cfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |