Primary Site >> Pancreatic Cancer
Gene >> CDH10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264463 |
| Start | 24505213:24505213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1292T>C |
| AA Mutation | p.Ile431Thr(p.I431T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264463 |
| Start | 24593430:24593430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.61T>A |
| AA Mutation | p.Ser21Thr(p.S21T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264463 |
| Start | 24487747:24487747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2283C>A |
| AA Mutation | p.Asn761Lys(p.N761K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264463 |
| Start | 24487994:24487994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2036C>T |
| AA Mutation | p.Ala679Val(p.A679V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264463 |
| Start | 24535763:24535763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.586G>A |
| AA Mutation | p.Ala196Thr(p.A196T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264463 |
| Start | 24535153:24535153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747981734 |
| CDS Mutation | c.773C>T |
| AA Mutation | p.Thr258Met(p.T258M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |