Primary Site >> Stomach Cancer
Gene >> PARN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000437198 |
| Start | 14446936:14446936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1816A>G |
| AA Mutation | p.Lys606Glu(p.K606E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000437198 |
| Start | 14610801:14610801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.397T>A |
| AA Mutation | p.Tyr133Asn(p.Y133N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000437198 |
| Start | 14593337:14593337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.882G>A |
| AA Mutation | p.Met294Ile(p.M294I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000437198 |
| Start | 14436737:14436737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750721134 |
| CDS Mutation | c.1900G>A |
| AA Mutation | p.Glu634Lys(p.E634K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000437198 |
| Start | 14446931:14446931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1821G>T |
| AA Mutation | p.Lys607Asn(p.K607N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000437198 |
| Start | 14617595:14617595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778795386 |
| CDS Mutation | c.383G>A |
| AA Mutation | p.Arg128Gln(p.R128Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000437198 |
| Start | 14482647:14482647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372489171 |
| CDS Mutation | c.1661G>A |
| AA Mutation | p.Arg554His(p.R554H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |