Primary Site >> Stomach Cancer
Gene >> TKTL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369915 |
| Start | 154315291:154315291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.983A>C |
| AA Mutation | p.Glu328Ala(p.E328A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369915 |
| Start | 154295876:154295876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371613816 |
| CDS Mutation | c.17C>T |
| AA Mutation | p.Ala6Val(p.A6V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369915 |
| Start | 154320763:154320763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372864317 |
| CDS Mutation | c.1036G>A |
| AA Mutation | p.Val346Met(p.V346M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369915 |
| Start | 154310862:154310862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782371916 |
| CDS Mutation | c.377A>T |
| AA Mutation | p.Asp126Val(p.D126V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369915 |
| Start | 154305344:154305344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.175G>A |
| AA Mutation | p.Val59Met(p.V59M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369915 |
| Start | 154320833:154320833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192912565 |
| CDS Mutation | c.1106G>A |
| AA Mutation | p.Arg369Gln(p.R369Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369915 |
| Start | 154327925:154327925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1585C>T |
| AA Mutation | p.Arg529Trp(p.R529W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369915 |
| Start | 154295864:154295864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782095901 |
| CDS Mutation | c.5C>T |
| AA Mutation | p.Ala2Val(p.A2V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369915 |
| Start | 154309373:154309373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.281G>A |
| AA Mutation | p.Gly94Glu(p.G94E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369915 |
| Start | 154329641:154329641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782727367 |
| CDS Mutation | c.1744A>G |
| AA Mutation | p.Ser582Gly(p.S582G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369915 |
| Start | 154312723:154312723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.814A>G |
| AA Mutation | p.Ile272Val(p.I272V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369915 |
| Start | 154323211:154323211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781847361 |
| CDS Mutation | c.1191C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |