Primary Site >> Stomach Cancer
Gene >> CAPN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000279247 |
| Start | 65204800:65204800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1283G>A |
| AA Mutation | p.Arg428His(p.R428H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000279247 |
| Start | 65183176:65183176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.316G>A |
| AA Mutation | p.Asp106Asn(p.D106N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000279247 |
| Start | 65204781:65204781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1264G>A |
| AA Mutation | p.Ala422Thr(p.A422T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000279247 |
| Start | 65206551:65206551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763471308 |
| CDS Mutation | c.1442G>A |
| AA Mutation | p.Arg481Gln(p.R481Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000279247 |
| Start | 65206526:65206526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762252249 |
| CDS Mutation | c.1417C>T |
| AA Mutation | p.Arg473Cys(p.R473C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000279247 |
| Start | 65209879:65209879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1825G>A |
| AA Mutation | p.Glu609Lys(p.E609K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000279247 |
| Start | 65210403:65210403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2010C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000279247 |
| Start | 65204819:65204819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1302C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000279247 |
| Start | 65185991:65185991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200853785 |
| CDS Mutation | c.531C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000279247 |
| Start | 65210400:65210400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377531394 |
| CDS Mutation | c.2007G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000279247 |
| Start | 65206516:65206516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745365536 |
| CDS Mutation | c.1407G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000279247 |
| Start | 65182737:65182737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.36T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |