Primary Site >> Stomach Cancer
Gene >> ITGB7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267082 |
| Start | 53192354:53192354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750166096 |
| CDS Mutation | c.2131G>A |
| AA Mutation | p.Val711Met(p.V711M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267082 |
| Start | 53191587:53191587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2366G>A |
| AA Mutation | p.Arg789His(p.R789H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267082 |
| Start | 53193163:53193163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747008975 |
| CDS Mutation | c.1703G>A |
| AA Mutation | p.Arg568Gln(p.R568Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267082 |
| Start | 53193841:53193841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1369C>A |
| AA Mutation | p.Leu457Ile(p.L457I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267082 |
| Start | 53193225:53193225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1641C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267082 |
| Start | 53192861:53192861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772827275 |
| CDS Mutation | c.1776G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |