Primary Site >> Stomach Cancer
Gene >> SLC7A5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261622 |
| Start | 87869188:87869188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.235G>A |
| AA Mutation | p.Ala79Thr(p.A79T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261622 |
| Start | 87836506:87836506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1282C>T |
| AA Mutation | p.Pro428Ser(p.P428S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261622 |
| Start | 87869122:87869122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.301C>T |
| AA Mutation | p.Leu101Phe(p.L101F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261622 |
| Start | 87832976:87832976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1518G>C |
| AA Mutation | p.Glu506Asp(p.E506D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261622 |
| Start | 87851781:87851781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151257488 |
| CDS Mutation | c.607G>A |
| AA Mutation | p.Ala203Thr(p.A203T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261622 |
| Start | 87836615:87836615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1173G>T |
| AA Mutation | p.Lys391Asn(p.K391N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261622 |
| Start | 87836602:87836602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149119495 |
| CDS Mutation | c.1186G>A |
| AA Mutation | p.Val396Ile(p.V396I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |