Primary Site >> Stomach Cancer
Gene >> CRX
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221996 |
| Start | 47839594:47839594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.527G>A |
| AA Mutation | p.Arg176Gln(p.R176Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221996 |
| Start | 47839501:47839501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.434C>A |
| AA Mutation | p.Pro145His(p.P145H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000221996 |
| Start | 47836245:47836245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778203784 |
| CDS Mutation | c.103G>A |
| AA Mutation | p.Ala35Thr(p.A35T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221996 |
| Start | 47839360:47839360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372219374 |
| CDS Mutation | c.293G>A |
| AA Mutation | p.Arg98Gln(p.R98Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221996 |
| Start | 47839794:47839794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.727G>A |
| AA Mutation | p.Gly243Arg(p.G243R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221996 |
| Start | 47839948:47839948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.881G>T |
| AA Mutation | p.Trp294Leu(p.W294L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221996 |
| Start | 47834486:47834486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559181643 |
| CDS Mutation | c.43G>A |
| AA Mutation | p.Ala15Thr(p.A15T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221996 |
| Start | 47839845:47839845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370592248 |
| CDS Mutation | c.778G>A |
| AA Mutation | p.Ala260Thr(p.A260T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221996 |
| Start | 47839632:47839632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142111462 |
| CDS Mutation | c.565G>A |
| AA Mutation | p.Ala189Thr(p.A189T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221996 |
| Start | 47839791:47839791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61748459 |
| CDS Mutation | c.724G>A |
| AA Mutation | p.Val242Met(p.V242M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |