Primary Site >> Esophagus Cancer
Gene >> REV3L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358835 |
| Start | 111373781:111373781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4574C>G |
| AA Mutation | p.Ser1525Cys(p.S1525C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358835 |
| Start | 111335498:111335498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7651T>G |
| AA Mutation | p.Phe2551Val(p.F2551V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358835 |
| Start | 111373676:111373676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775832892 |
| CDS Mutation | c.4679A>G |
| AA Mutation | p.Asn1560Ser(p.N1560S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358835 |
| Start | 111375113:111375113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3242C>T |
| AA Mutation | p.Ser1081Leu(p.S1081L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358835 |
| Start | 111333352:111333352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368840674 |
| CDS Mutation | c.7696A>G |
| AA Mutation | p.Met2566Val(p.M2566V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358835 |
| Start | 111374228:111374228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4127C>T |
| AA Mutation | p.Ser1376Phe(p.S1376F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358835 |
| Start | 111374976:111374976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757261538 |
| CDS Mutation | c.3379C>T |
| AA Mutation | p.Arg1127Cys(p.R1127C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358835 |
| Start | 111389123:111389123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.845G>A |
| AA Mutation | p.Ser282Asn(p.S282N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358835 |
| Start | 111373745:111373745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4610G>T |
| AA Mutation | p.Arg1537Ile(p.R1537I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358835 |
| Start | 111373794:111373794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4561G>T |
| AA Mutation | p.Gly1521Cys(p.G1521C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358835 |
| Start | 111363904:111363904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755842391 |
| CDS Mutation | c.6828C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |