Primary Site >> Stomach Cancer
Gene >> PCOLCE2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295992 |
| Start | 142848238:142848238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376768304 |
| CDS Mutation | c.427G>A |
| AA Mutation | p.Ala143Thr(p.A143T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295992 |
| Start | 142842989:142842989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.508T>A |
| AA Mutation | p.Trp170Arg(p.W170R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295992 |
| Start | 142820904:142820904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776696030 |
| CDS Mutation | c.1091G>A |
| AA Mutation | p.Cys364Tyr(p.C364Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295992 |
| Start | 142848352:142848352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.313C>T |
| AA Mutation | p.Arg105Cys(p.R105C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295992 |
| Start | 142848242:142848242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.423C>A |
| AA Mutation | p.Phe141Leu(p.F141L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295992 |
| Start | 142820908:142820908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762154075 |
| CDS Mutation | c.1087G>A |
| AA Mutation | p.Val363Ile(p.V363I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295992 |
| Start | 142848414:142848414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.251A>G |
| AA Mutation | p.Asn84Ser(p.N84S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295992 |
| Start | 142848370:142848370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.295A>G |
| AA Mutation | p.Asn99Asp(p.N99D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295992 |
| Start | 142887746:142887746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.115G>A |
| AA Mutation | p.Gly39Arg(p.G39R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295992 |
| Start | 142848378:142848378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749519201 |
| CDS Mutation | c.287G>A |
| AA Mutation | p.Gly96Asp(p.G96D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |