Primary Site >> Stomach Cancer
Gene >> SELE
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333360 |
| Start | 169732870:169732870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.166A>G |
| AA Mutation | p.Ile56Val(p.I56V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333360 |
| Start | 169727420:169727420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752904063 |
| CDS Mutation | c.1574C>T |
| AA Mutation | p.Thr525Met(p.T525M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333360 |
| Start | 169725763:169725763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1814A>G |
| AA Mutation | p.Lys605Arg(p.K605R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333360 |
| Start | 169727421:169727421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1573A>G |
| AA Mutation | p.Thr525Ala(p.T525A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333360 |
| Start | 169727418:169727418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1576C>T |
| AA Mutation | p.Leu526Phe(p.L526F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333360 |
| Start | 169731910:169731910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143566739 |
| CDS Mutation | c.454G>A |
| AA Mutation | p.Gly152Ser(p.G152S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333360 |
| Start | 169731920:169731920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.444C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333360 |
| Start | 169730439:169730439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.708C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333360 |
| Start | 169727506:169727506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1488G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333360 |
| Start | 169727917:169727917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779988614 |
| CDS Mutation | c.1290C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000333360 |
| Start | 169732810:169732810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.226A>T |
| AA Mutation | p.Lys76Ter(p.K76*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |