Primary Site >> Stomach Cancer
Gene >> KCNK15
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372861 |
| Start | 44745963:44745963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.53A>G |
| AA Mutation | p.Tyr18Cys(p.Y18C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372861 |
| Start | 44750479:44750479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.634G>A |
| AA Mutation | p.Glu212Lys(p.E212K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372861 |
| Start | 44750159:44750159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.314C>A |
| AA Mutation | p.Ser105Tyr(p.S105Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372861 |
| Start | 44750539:44750539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.694C>A |
| AA Mutation | p.Leu232Ile(p.L232I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372861 |
| Start | 44750237:44750237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.392G>A |
| AA Mutation | p.Arg131Gln(p.R131Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372861 |
| Start | 44750257:44750257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.412C>T |
| AA Mutation | p.Arg138Cys(p.R138C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372861 |
| Start | 44750451:44750451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.606C>G |
| AA Mutation | p.Phe202Leu(p.F202L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372861 |
| Start | 44750634:44750634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373771578 |
| CDS Mutation | c.789G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372861 |
| Start | 44750475:44750475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.630C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000372861 |
| Start | 44750637:44750637(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.797delC |
| AA Mutation | p.Pro266ArgfsTer99(p.P266Rfs*99) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000372861 |
| Start | 44750636:44750637(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs768101521 |
| CDS Mutation | c.797dupC |
| AA Mutation | p.Ala268GlyfsTer94(p.A268Gfs*94) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |