Primary Site >> Stomach Cancer
Gene >> SEL1L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336735 |
| Start | 81477102:81477102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141918133 |
| CDS Mutation | c.2255C>T |
| AA Mutation | p.Ala752Val(p.A752V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336735 |
| Start | 81487858:81487858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1480T>C |
| AA Mutation | p.Tyr494His(p.Y494H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336735 |
| Start | 81477024:81477024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376067391 |
| CDS Mutation | c.2333G>A |
| AA Mutation | p.Arg778Gln(p.R778Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336735 |
| Start | 81506141:81506141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.441A>C |
| AA Mutation | p.Glu147Asp(p.E147D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336735 |
| Start | 81486427:81486427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1660C>T |
| AA Mutation | p.Arg554Cys(p.R554C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336735 |
| Start | 81526752:81526752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.321A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336735 |
| Start | 81479648:81479648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765245803 |
| CDS Mutation | c.2139C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336735 |
| Start | 81486380:81486380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753470397 |
| CDS Mutation | c.1707C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000336735 |
| Start | 81486433:81486433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777962520 |
| CDS Mutation | c.1654C>T |
| AA Mutation | p.Arg552Ter(p.R552*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000336735 |
| Start | 81487413:81487413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756319106 |
| CDS Mutation | c.1609C>T |
| AA Mutation | p.Arg537Ter(p.R537*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |