Primary Site >> Stomach Cancer
Gene >> SP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327443 |
| Start | 53382213:53382213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773597100 |
| CDS Mutation | c.266G>A |
| AA Mutation | p.Gly89Glu(p.G89E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327443 |
| Start | 53382366:53382366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.419G>A |
| AA Mutation | p.Arg140His(p.R140H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327443 |
| Start | 53382869:53382869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.922G>A |
| AA Mutation | p.Ala308Thr(p.A308T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327443 |
| Start | 53382512:53382512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532028059 |
| CDS Mutation | c.565T>C |
| AA Mutation | p.Phe189Leu(p.F189L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327443 |
| Start | 53383451:53383451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1504C>G |
| AA Mutation | p.Leu502Val(p.L502V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327443 |
| Start | 53382483:53382483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.536T>C |
| AA Mutation | p.Phe179Ser(p.F179S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327443 |
| Start | 53383615:53383615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755108127 |
| CDS Mutation | c.1668T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327443 |
| Start | 53382934:53382934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764626059 |
| CDS Mutation | c.987T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327443 |
| Start | 53382400:53382400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146930500 |
| CDS Mutation | c.453C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |