Primary Site >> Stomach Cancer
Gene >> GGT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248923 |
| Start | 24628180:24628180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752649541 |
| CDS Mutation | c.1436C>T |
| AA Mutation | p.Thr479Met(p.T479M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248923 |
| Start | 24614786:24614786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367703847 |
| CDS Mutation | c.175C>T |
| AA Mutation | p.Arg59Trp(p.R59W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248923 |
| Start | 24628831:24628831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1702G>A |
| AA Mutation | p.Gly568Ser(p.G568S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248923 |
| Start | 24623845:24623845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757411384 |
| CDS Mutation | c.949G>A |
| AA Mutation | p.Val317Ile(p.V317I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248923 |
| Start | 24628799:24628799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1670C>T |
| AA Mutation | p.Ala557Val(p.A557V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248923 |
| Start | 24628110:24628110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1366A>T |
| AA Mutation | p.Thr456Ser(p.T456S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248923 |
| Start | 24627462:24627462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754122506 |
| CDS Mutation | c.1051G>A |
| AA Mutation | p.Ala351Thr(p.A351T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248923 |
| Start | 24623868:24623868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770009570 |
| CDS Mutation | c.972C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248923 |
| Start | 24611144:24611144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.63C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248923 |
| Start | 24614791:24614791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs191957455 |
| CDS Mutation | c.180C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248923 |
| Start | 24623189:24623189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.816G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248923 |
| Start | 24628097:24628097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766264249 |
| CDS Mutation | c.1353G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |