Primary Site >> Pancreatic Cancer
Gene >> OBSCN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422127 |
| Start | 228292744:228292744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374049885 |
| CDS Mutation | c.10825G>A |
| AA Mutation | p.Val3609Met(p.V3609M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422127 |
| Start | 228287846:228287846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367605500 |
| CDS Mutation | c.9697C>T |
| AA Mutation | p.Arg3233Cys(p.R3233C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422127 |
| Start | 228244313:228244313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3223G>T |
| AA Mutation | p.Ala1075Ser(p.A1075S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422127 |
| Start | 228268562:228268562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4894G>T |
| AA Mutation | p.Ala1632Ser(p.A1632S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000422127 |
| Start | 228288887:228288887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10338G>T |
| AA Mutation | p.Lys3446Asn(p.K3446N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422127 |
| Start | 228316744:228316744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13321G>A |
| AA Mutation | p.Ala4441Thr(p.A4441T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000422127 |
| Start | 228280179:228280179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769945926 |
| CDS Mutation | c.7664C>T |
| AA Mutation | p.Ala2555Val(p.A2555V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000422127 |
| Start | 228280181:228280181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566340039 |
| CDS Mutation | c.7666C>T |
| AA Mutation | p.Arg2556Trp(p.R2556W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422127 |
| Start | 228374636:228374636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.22547A>G |
| AA Mutation | p.Lys7516Arg(p.K7516R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422127 |
| Start | 228250120:228250120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4189C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422127 |
| Start | 228283726:228283726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570299277 |
| CDS Mutation | c.8961C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422127 |
| Start | 228293531:228293531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11046G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422127 |
| Start | 228323596:228323596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15642C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422127 |
| Start | 228377977:228377977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.23550C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422127 |
| Start | 228292040:228292040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776647460 |
| CDS Mutation | c.10482C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000422127 |
| Start | 228338145:228338145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.17001+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |