Primary Site >> Stomach Cancer
Gene >> CLASP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263710 |
| Start | 121367680:121367680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3794A>G |
| AA Mutation | p.Asn1265Ser(p.N1265S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263710 |
| Start | 121401555:121401555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2854C>T |
| AA Mutation | p.Leu952Phe(p.L952F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263710 |
| Start | 121515699:121515699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.610G>A |
| AA Mutation | p.Ala204Thr(p.A204T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263710 |
| Start | 121457697:121457697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1375G>A |
| AA Mutation | p.Ala459Thr(p.A459T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263710 |
| Start | 121407688:121407688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2452C>T |
| AA Mutation | p.Pro818Ser(p.P818S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263710 |
| Start | 121407663:121407663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2477A>G |
| AA Mutation | p.Asp826Gly(p.D826G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263710 |
| Start | 121397156:121397156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3107G>A |
| AA Mutation | p.Ser1036Asn(p.S1036N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263710 |
| Start | 121528696:121528696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.359A>G |
| AA Mutation | p.Asp120Gly(p.D120G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263710 |
| Start | 121528764:121528764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.291A>G |
| AA Mutation | p.Ile97Met(p.I97M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263710 |
| Start | 121605757:121605757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.139T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263710 |
| Start | 121387199:121387199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368237661 |
| CDS Mutation | c.3297G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263710 |
| Start | 121459985:121459985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377669982 |
| CDS Mutation | c.1173G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263710 |
| Start | 121367782:121367782(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs749719822 |
| CDS Mutation | c.3692delG |
| AA Mutation | p.Gly1231ValfsTer4(p.G1231Vfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |