Primary Site >> Stomach Cancer
Gene >> SEZ6L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248933 |
| Start | 26340624:26340624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2204A>G |
| AA Mutation | p.Asn735Ser(p.N735S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248933 |
| Start | 26351103:26351103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762219064 |
| CDS Mutation | c.2459C>T |
| AA Mutation | p.Ser820Leu(p.S820L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248933 |
| Start | 26351225:26351225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779505302 |
| CDS Mutation | c.2581C>T |
| AA Mutation | p.Arg861Cys(p.R861C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248933 |
| Start | 26313823:26313823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752901613 |
| CDS Mutation | c.1936G>A |
| AA Mutation | p.Glu646Lys(p.E646K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248933 |
| Start | 26306104:26306104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1474C>T |
| AA Mutation | p.His492Tyr(p.H492Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248933 |
| Start | 26297032:26297032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753580054 |
| CDS Mutation | c.1114C>T |
| AA Mutation | p.Arg372Trp(p.R372W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248933 |
| Start | 26347832:26347832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748996632 |
| CDS Mutation | c.2326G>A |
| AA Mutation | p.Gly776Ser(p.G776S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248933 |
| Start | 26292647:26292647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.336C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248933 |
| Start | 26310730:26310730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186497116 |
| CDS Mutation | c.1575C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248933 |
| Start | 26306016:26306016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1386C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248933 |
| Start | 26351071:26351071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374698416 |
| CDS Mutation | c.2427C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248933 |
| Start | 26351221:26351221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755130730 |
| CDS Mutation | c.2577G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |