Primary Site >> Pancreatic Cancer
Gene >> GRIN2B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13567183:13567183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2440G>A |
| AA Mutation | p.Asp814Asn(p.D814N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13753462:13753462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.865C>T |
| AA Mutation | p.Leu289Phe(p.L289F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13564005:13564005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3233C>T |
| AA Mutation | p.Ala1078Val(p.A1078V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13564599:13564599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2639G>A |
| AA Mutation | p.Arg880His(p.R880H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563629:13563629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3609C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13675790:13675790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201952040 |
| CDS Mutation | c.1080G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13564082:13564082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543452359 |
| CDS Mutation | c.3156C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |