Primary Site >> Stomach Cancer
Gene >> ITLN2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368029 |
| Start | 160952637:160952637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530710369 |
| CDS Mutation | c.176G>A |
| AA Mutation | p.Arg59His(p.R59H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368029 |
| Start | 160945186:160945186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.932G>A |
| AA Mutation | p.Cys311Tyr(p.C311Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368029 |
| Start | 160951216:160951216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368397499 |
| CDS Mutation | c.268G>A |
| AA Mutation | p.Gly90Ser(p.G90S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368029 |
| Start | 160951108:160951108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777694118 |
| CDS Mutation | c.376G>A |
| AA Mutation | p.Asp126Asn(p.D126N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368029 |
| Start | 160945226:160945226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.892T>C |
| AA Mutation | p.Phe298Leu(p.F298L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368029 |
| Start | 160945179:160945179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.939G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368029 |
| Start | 160947974:160947974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781228362 |
| CDS Mutation | c.780C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |