Primary Site >> Stomach Cancer
Gene >> KCNK5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359534 |
| Start | 39195897:39195897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.277G>A |
| AA Mutation | p.Ala93Thr(p.A93T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359534 |
| Start | 39191729:39191729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757159016 |
| CDS Mutation | c.661G>A |
| AA Mutation | p.Ala221Thr(p.A221T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359534 |
| Start | 39191428:39191428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145388113 |
| CDS Mutation | c.962C>T |
| AA Mutation | p.Thr321Met(p.T321M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359534 |
| Start | 39194184:39194184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779600138 |
| CDS Mutation | c.619G>A |
| AA Mutation | p.Gly207Ser(p.G207S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359534 |
| Start | 39194243:39194243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.560G>T |
| AA Mutation | p.Gly187Val(p.G187V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359534 |
| Start | 39229086:39229086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.26C>A |
| AA Mutation | p.Thr9Asn(p.T9N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359534 |
| Start | 39228997:39228997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.115T>C |
| AA Mutation | p.Tyr39His(p.Y39H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359534 |
| Start | 39191097:39191097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144931567 |
| CDS Mutation | c.1293C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359534 |
| Start | 39191390:39191391(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.999dupG |
| AA Mutation | p.Leu334AlafsTer41(p.L334Afs*41) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |