Primary Site >> Stomach Cancer
Gene >> SRL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399609 |
| Start | 4197874:4197874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.301C>T |
| AA Mutation | p.Pro101Ser(p.P101S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399609 |
| Start | 4242030:4242030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.38C>T |
| AA Mutation | p.Ser13Leu(p.S13L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399609 |
| Start | 4192608:4192608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373144625 |
| CDS Mutation | c.967G>A |
| AA Mutation | p.Glu323Lys(p.E323K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399609 |
| Start | 4192614:4192614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.961G>C |
| AA Mutation | p.Val321Leu(p.V321L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399609 |
| Start | 4242060:4242060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374732804 |
| CDS Mutation | c.8C>T |
| AA Mutation | p.Ala3Val(p.A3V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399609 |
| Start | 4192550:4192550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1025T>C |
| AA Mutation | p.Ile342Thr(p.I342T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000399609 |
| Start | 4197797:4197797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112367857 |
| CDS Mutation | c.376+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |