Primary Site >> Stomach Cancer
Gene >> EGR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242480 |
| Start | 62813682:62813682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.956C>A |
| AA Mutation | p.Pro319His(p.P319H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242480 |
| Start | 62814360:62814360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200488421 |
| CDS Mutation | c.278T>C |
| AA Mutation | p.Met93Thr(p.M93T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242480 |
| Start | 62813443:62813443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1195G>A |
| AA Mutation | p.Ala399Thr(p.A399T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242480 |
| Start | 62813860:62813860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.778C>T |
| AA Mutation | p.Pro260Ser(p.P260S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242480 |
| Start | 62813458:62813458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1180G>A |
| AA Mutation | p.Gly394Ser(p.G394S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242480 |
| Start | 62814339:62814339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.299C>A |
| AA Mutation | p.Pro100His(p.P100H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242480 |
| Start | 62813385:62813385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1253A>C |
| AA Mutation | p.Lys418Thr(p.K418T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242480 |
| Start | 62813713:62813713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.925G>A |
| AA Mutation | p.Ala309Thr(p.A309T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242480 |
| Start | 62813520:62813520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1118G>A |
| AA Mutation | p.Arg373Gln(p.R373Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000242480 |
| Start | 62813270:62813270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1368T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000242480 |
| Start | 62813714:62813714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.924C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000242480 |
| Start | 62814077:62814077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144739493 |
| CDS Mutation | c.561G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000242480 |
| Start | 62813729:62813729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112474655 |
| CDS Mutation | c.909A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |