Primary Site >> Stomach Cancer
Gene >> SLC13A5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433363 |
| Start | 6703973:6703973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.452T>A |
| AA Mutation | p.Ile151Asn(p.I151N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433363 |
| Start | 6687537:6687537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1567G>A |
| AA Mutation | p.Ala523Thr(p.A523T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433363 |
| Start | 6703066:6703066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.620C>A |
| AA Mutation | p.Ala207Asp(p.A207D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433363 |
| Start | 6703052:6703052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.634A>G |
| AA Mutation | p.Ile212Val(p.I212V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433363 |
| Start | 6703010:6703010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.676G>C |
| AA Mutation | p.Gly226Arg(p.G226R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433363 |
| Start | 6703953:6703953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.472C>A |
| AA Mutation | p.Gln158Lys(p.Q158K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433363 |
| Start | 6695897:6695897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.884A>G |
| AA Mutation | p.Glu295Gly(p.E295G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433363 |
| Start | 6703061:6703061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.625A>G |
| AA Mutation | p.Thr209Ala(p.T209A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433363 |
| Start | 6690880:6690880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1336G>A |
| AA Mutation | p.Ala446Thr(p.A446T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433363 |
| Start | 6695745:6695745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1036T>C |
| AA Mutation | p.Trp346Arg(p.W346R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433363 |
| Start | 6703085:6703085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142320179 |
| CDS Mutation | c.601C>T |
| AA Mutation | p.Arg201Trp(p.R201W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000433363 |
| Start | 6703936:6703936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372231184 |
| CDS Mutation | c.489C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |