Primary Site >> Pancreatic Cancer
Gene >> ITPR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354582 |
| Start | 4676673:4676673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777634985 |
| CDS Mutation | c.2839C>T |
| AA Mutation | p.Arg947Trp(p.R947W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354582 |
| Start | 4680655:4680655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3070G>A |
| AA Mutation | p.Gly1024Arg(p.G1024R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354582 |
| Start | 4706287:4706287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4778C>T |
| AA Mutation | p.Ala1593Val(p.A1593V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354582 |
| Start | 4806181:4806181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7186C>A |
| AA Mutation | p.Leu2396Met(p.L2396M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354582 |
| Start | 4811293:4811293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7301C>T |
| AA Mutation | p.Thr2434Ile(p.T2434I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354582 |
| Start | 4702848:4702848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4555G>T |
| AA Mutation | p.Val1519Leu(p.V1519L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354582 |
| Start | 4795120:4795120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370852124 |
| CDS Mutation | c.6864G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |