Primary Site >> Esophagus Cancer
Gene >> NBAS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15511306:15511306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149760582 |
| CDS Mutation | c.791C>T |
| AA Mutation | p.Ser264Leu(p.S264L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15475695:15475695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751468811 |
| CDS Mutation | c.1333A>T |
| AA Mutation | p.Ser445Cys(p.S445C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15218783:15218783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6422C>T |
| AA Mutation | p.Pro2141Leu(p.P2141L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000281513 |
| Start | 15474148:15474148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1518G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000281513 |
| Start | 15238663:15238663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5748G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000281513 |
| Start | 15504175:15504175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774810902 |
| CDS Mutation | c.924C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000281513 |
| Start | 15554123:15554124(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs771933634 |
| CDS Mutation | c.224dupT |
| AA Mutation | p.Leu75PhefsTer4(p.L75Ffs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |