Primary Site >> Stomach Cancer
Gene >> ERGIC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393784 |
| Start | 172932526:172932526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.632T>A |
| AA Mutation | p.Val211Glu(p.V211E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393784 |
| Start | 172914767:172914767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766575211 |
| CDS Mutation | c.304G>A |
| AA Mutation | p.Asp102Asn(p.D102N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393784 |
| Start | 172914810:172914810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369010301 |
| CDS Mutation | c.347G>A |
| AA Mutation | p.Arg116His(p.R116H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393784 |
| Start | 172888707:172888707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.29T>G |
| AA Mutation | p.Ile10Ser(p.I10S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393784 |
| Start | 172888750:172888750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149114698 |
| CDS Mutation | c.72C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393784 |
| Start | 172888744:172888744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760955420 |
| CDS Mutation | c.66G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393784 |
| Start | 172897042:172897042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.123C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393784 |
| Start | 172950765:172950765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.822C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |