Primary Site >> Esophagus Cancer
Gene >> GNAS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58905428:58905428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.478C>T |
| AA Mutation | p.Arg160Cys(p.R160C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58853412:58853412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.147G>A |
| AA Mutation | p.Met49Ile(p.M49I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58909389:58909389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.625G>C |
| AA Mutation | p.Glu209Gln(p.E209Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58853404:58853404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.139G>A |
| AA Mutation | p.Glu47Lys(p.E47K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58909365:58909365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs11554273 |
| CDS Mutation | c.601C>T |
| AA Mutation | p.Arg201Cys(p.R201C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58853446:58853446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587778390 |
| CDS Mutation | c.181G>A |
| AA Mutation | p.Val61Ile(p.V61I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58909366:58909366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913495 |
| CDS Mutation | c.602G>A |
| AA Mutation | p.Arg201His(p.R201H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58910012:58910012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.901G>T |
| AA Mutation | p.Val301Phe(p.V301F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58853526:58853526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.261A>C |
| AA Mutation | p.Glu87Asp(p.E87D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371100 |
| Start | 58854222:58854222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.957C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371100 |
| Start | 58855125:58855125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199549396 |
| CDS Mutation | c.1860C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000371100 |
| Start | 58855144:58855144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1879C>T |
| AA Mutation | p.Gln627Ter(p.Q627*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |