Primary Site >> Stomach Cancer
Gene >> AKT2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392038 |
| Start | 40237995:40237995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763951605 |
| CDS Mutation | c.805C>T |
| AA Mutation | p.Arg269Trp(p.R269W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392038 |
| Start | 40256932:40256932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.169G>A |
| AA Mutation | p.Val57Ile(p.V57I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392038 |
| Start | 40241976:40241976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.535G>A |
| AA Mutation | p.Ala179Thr(p.A179T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392038 |
| Start | 40240053:40240053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.631T>C |
| AA Mutation | p.Phe211Leu(p.F211L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392038 |
| Start | 40265251:40265251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.17T>C |
| AA Mutation | p.Val6Ala(p.V6A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392038 |
| Start | 40241943:40241943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.568G>A |
| AA Mutation | p.Ala190Thr(p.A190T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392038 |
| Start | 40257027:40257027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746989021 |
| CDS Mutation | c.74G>A |
| AA Mutation | p.Arg25Gln(p.R25Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392038 |
| Start | 40236025:40236025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202125073 |
| CDS Mutation | c.1040G>A |
| AA Mutation | p.Arg347His(p.R347H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392038 |
| Start | 40242003:40242003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs572670425 |
| CDS Mutation | c.508C>T |
| AA Mutation | p.Arg170Trp(p.R170W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392038 |
| Start | 40235115:40235115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs56098986 |
| CDS Mutation | c.1296C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000392038 |
| Start | 40256948:40256948(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.153delC |
| AA Mutation | p.Leu52Ter(p.L52*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |