Primary Site >> Stomach Cancer
Gene >> MYLIP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356840 |
| Start | 16141641:16141641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.295C>T |
| AA Mutation | p.His99Tyr(p.H99Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356840 |
| Start | 16145072:16145072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201087709 |
| CDS Mutation | c.1003G>A |
| AA Mutation | p.Val335Ile(p.V335I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356840 |
| Start | 16145036:16145036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.967T>C |
| AA Mutation | p.Tyr323His(p.Y323H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356840 |
| Start | 16143166:16143166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.611T>C |
| AA Mutation | p.Val204Ala(p.V204A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356840 |
| Start | 16145306:16145306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs531259441 |
| CDS Mutation | c.1237G>A |
| AA Mutation | p.Ala413Thr(p.A413T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356840 |
| Start | 16141757:16141757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.411G>T |
| AA Mutation | p.Lys137Asn(p.K137N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356840 |
| Start | 16143724:16143724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.688G>A |
| AA Mutation | p.Ala230Thr(p.A230T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356840 |
| Start | 16143140:16143140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189481765 |
| CDS Mutation | c.585C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356840 |
| Start | 16130631:16130631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.162A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356840 |
| Start | 16146700:16146700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1287G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356840 |
| Start | 16143095:16143095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370693513 |
| CDS Mutation | c.540G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |