Primary Site >> Stomach Cancer
Gene >> SLC52A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329994 |
| Start | 144360806:144360806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1129C>A |
| AA Mutation | p.Leu377Met(p.L377M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329994 |
| Start | 144359917:144359917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs560681538 |
| CDS Mutation | c.425G>A |
| AA Mutation | p.Arg142His(p.R142H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329994 |
| Start | 144360912:144360912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1235T>C |
| AA Mutation | p.Ile412Thr(p.I412T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329994 |
| Start | 144360069:144360069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781928955 |
| CDS Mutation | c.577G>A |
| AA Mutation | p.Ala193Thr(p.A193T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329994 |
| Start | 144360241:144360241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.749T>C |
| AA Mutation | p.Leu250Pro(p.L250P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329994 |
| Start | 144359648:144359648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.156T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329994 |
| Start | 144360113:144360113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.621A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329994 |
| Start | 144359317:144359317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.24T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329994 |
| Start | 144360841:144360841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370533575 |
| CDS Mutation | c.1164C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |