Primary Site >> Stomach Cancer
Gene >> SPHK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245222 |
| Start | 48629339:48629339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1531T>A |
| AA Mutation | p.Ser511Thr(p.S511T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245222 |
| Start | 48628884:48628884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1076C>T |
| AA Mutation | p.Thr359Ile(p.T359I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245222 |
| Start | 48626221:48626221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778819049 |
| CDS Mutation | c.370C>T |
| AA Mutation | p.Arg124Trp(p.R124W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245222 |
| Start | 48629629:48629629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1821C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245222 |
| Start | 48628693:48628693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.885C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245222 |
| Start | 48628927:48628927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148911321 |
| CDS Mutation | c.1119C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245222 |
| Start | 48628825:48628825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1017C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000245222 |
| Start | 48628273:48628273(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.872+1delG |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000245222 |
| Start | 48628272:48628273(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs748435598 |
| CDS Mutation | c.872+1dupG |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |