Primary Site >> Pancreatic Cancer
Gene >> KALRN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124094858:124094858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.21C>G |
| AA Mutation | p.Asp7Glu(p.D7E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124334377:124334377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1523T>C |
| AA Mutation | p.Leu508Pro(p.L508P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124398824:124398824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2293C>A |
| AA Mutation | p.Leu765Met(p.L765M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240874 |
| Start | 124492876:124492876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4820G>T |
| AA Mutation | p.Ser1607Ile(p.S1607I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360013 |
| Start | 124562889:124562889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769031992 |
| CDS Mutation | c.4976C>T |
| AA Mutation | p.Ala1659Val(p.A1659V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240874 |
| Start | 124430659:124430659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138919966 |
| CDS Mutation | c.2707C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291478 |
| Start | 124661919:124661919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1242G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000240874 |
| Start | 124234843:124234843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.157C>T |
| AA Mutation | p.Arg53Ter(p.R53*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |