Primary Site >> Stomach Cancer
Gene >> ITIH4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266041 |
| Start | 52826819:52826819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377477789 |
| CDS Mutation | c.491G>A |
| AA Mutation | p.Arg164Gln(p.R164Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266041 |
| Start | 52823972:52823972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs74971919 |
| CDS Mutation | c.1204G>A |
| AA Mutation | p.Val402Met(p.V402M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266041 |
| Start | 52826820:52826820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.490C>T |
| AA Mutation | p.Arg164Trp(p.R164W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266041 |
| Start | 52826889:52826889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.421A>G |
| AA Mutation | p.Thr141Ala(p.T141A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266041 |
| Start | 52829213:52829213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs572371573 |
| CDS Mutation | c.157G>A |
| AA Mutation | p.Val53Ile(p.V53I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266041 |
| Start | 52820778:52820778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569565296 |
| CDS Mutation | c.1687G>A |
| AA Mutation | p.Ala563Thr(p.A563T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266041 |
| Start | 52813485:52813485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113454148 |
| CDS Mutation | c.2729G>A |
| AA Mutation | p.Arg910His(p.R910H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266041 |
| Start | 52816904:52816904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755043796 |
| CDS Mutation | c.2451G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266041 |
| Start | 52824274:52824274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1087C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266041 |
| Start | 52825934:52825934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.711C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266041 |
| Start | 52827131:52827131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765070219 |
| CDS Mutation | c.318C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |