Primary Site >> Esophagus Cancer
Gene >> HSPG2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21859933:21859933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5084C>T |
| AA Mutation | p.Ser1695Phe(p.S1695F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21842778:21842778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8902C>G |
| AA Mutation | p.Arg2968Gly(p.R2968G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21862058:21862058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201665758 |
| CDS Mutation | c.4798G>A |
| AA Mutation | p.Gly1600Arg(p.G1600R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21834786:21834786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10613G>A |
| AA Mutation | p.Gly3538Asp(p.G3538D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21878614:21878614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2521G>A |
| AA Mutation | p.Ala841Thr(p.A841T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21895936:21895936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.230G>C |
| AA Mutation | p.Gly77Ala(p.G77A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21828906:21828906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12166G>C |
| AA Mutation | p.Gly4056Arg(p.G4056R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21848696:21848696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755215244 |
| CDS Mutation | c.7684C>T |
| AA Mutation | p.Pro2562Ser(p.P2562S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374695 |
| Start | 21855896:21855896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376398201 |
| CDS Mutation | c.5592C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374695 |
| Start | 21842309:21842309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143921375 |
| CDS Mutation | c.8982C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374695 |
| Start | 21841609:21841609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142555110 |
| CDS Mutation | c.9258C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374695 |
| Start | 21896200:21896201(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.170_173dupAGGA |
| AA Mutation | p.Asp58GlufsTer6(p.D58Efs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |