Primary Site >> Liver Cancer
Gene >> SPTBN2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309996 |
| Start | 66688835:66688835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6049G>T |
| AA Mutation | p.Val2017Leu(p.V2017L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309996 |
| Start | 66708182:66708182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1309C>T |
| AA Mutation | p.Arg437Trp(p.R437W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309996 |
| Start | 66705410:66705410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1866C>G |
| AA Mutation | p.Ser622Arg(p.S622R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309996 |
| Start | 66696425:66696425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767535278 |
| CDS Mutation | c.4130G>A |
| AA Mutation | p.Arg1377His(p.R1377H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309996 |
| Start | 66700872:66700872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3227A>T |
| AA Mutation | p.Asp1076Val(p.D1076V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309996 |
| Start | 66715925:66715925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.214G>T |
| AA Mutation | p.Ala72Ser(p.A72S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309996 |
| Start | 66693284:66693284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4756G>T |
| AA Mutation | p.Asp1586Tyr(p.D1586Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309996 |
| Start | 66704827:66704827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2449C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309996 |
| Start | 66705772:66705772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148207416 |
| CDS Mutation | c.1719C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000309996 |
| Start | 66699084:66699084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3777-2A>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |