Primary Site >> Stomach Cancer
Gene >> IGF2BP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382199 |
| Start | 185645613:185645613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750722399 |
| CDS Mutation | c.1718G>A |
| AA Mutation | p.Arg573His(p.R573H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382199 |
| Start | 185645538:185645538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1793G>A |
| AA Mutation | p.Ser598Asn(p.S598N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382199 |
| Start | 185689433:185689433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.599T>C |
| AA Mutation | p.Val200Ala(p.V200A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382199 |
| Start | 185649525:185649525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1471C>T |
| AA Mutation | p.Arg491Trp(p.R491W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382199 |
| Start | 185672579:185672579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771848248 |
| CDS Mutation | c.1162C>T |
| AA Mutation | p.Arg388Cys(p.R388C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382199 |
| Start | 185696653:185696653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.299G>C |
| AA Mutation | p.Gly100Ala(p.G100A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382199 |
| Start | 185675823:185675823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.903A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382199 |
| Start | 185652145:185652145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147590133 |
| CDS Mutation | c.1410C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382199 |
| Start | 185687104:185687104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.765C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382199 |
| Start | 185657352:185657352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142081639 |
| CDS Mutation | c.1320C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382199 |
| Start | 185649445:185649445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1551C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382199 |
| Start | 185689525:185689525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.507C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382199 |
| Start | 185672571:185672571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1170T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382199 |
| Start | 185689447:185689447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746680034 |
| CDS Mutation | c.585G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000382199 |
| Start | 185698328:185698328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772496480 |
| CDS Mutation | c.259C>T |
| AA Mutation | p.Arg87Ter(p.R87*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |