Primary Site >> Stomach Cancer
Gene >> SLC2A6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371899 |
| Start | 133472025:133472025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370809335 |
| CDS Mutation | c.1520G>A |
| AA Mutation | p.Arg507His(p.R507H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371899 |
| Start | 133475419:133475419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.755A>C |
| AA Mutation | p.Gln252Pro(p.Q252P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371899 |
| Start | 133472139:133472139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146699447 |
| CDS Mutation | c.1406C>T |
| AA Mutation | p.Ala469Val(p.A469V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371899 |
| Start | 133472116:133472116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1429G>A |
| AA Mutation | p.Val477Met(p.V477M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371899 |
| Start | 133474052:133474052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781878936 |
| CDS Mutation | c.964C>T |
| AA Mutation | p.Arg322Trp(p.R322W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371899 |
| Start | 133473421:133473421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1216A>G |
| AA Mutation | p.Ile406Val(p.I406V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371899 |
| Start | 133476262:133476262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782152058 |
| CDS Mutation | c.537C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371899 |
| Start | 133478400:133478400(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.109delA |
| AA Mutation | p.Arg37GlyfsTer40(p.R37Gfs*40) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371899 |
| Start | 133476296:133476297(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.502dupG |
| AA Mutation | p.Ala168GlyfsTer99(p.A168Gfs*99) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000371899 |
| Start | 133472099:133472100(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1443_1445dupCTG |
| AA Mutation | p.Cys482dup(p.C482dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |