Primary Site >> Esophagus Cancer
Gene >> FOXG1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768405:28768405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1126A>G |
| AA Mutation | p.Thr376Ala(p.T376A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768009:28768009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.730C>A |
| AA Mutation | p.Arg244Ser(p.R244S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768663:28768663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1384A>C |
| AA Mutation | p.Ser462Arg(p.S462R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768663:28768663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752379833 |
| CDS Mutation | c.1384A>G |
| AA Mutation | p.Ser462Gly(p.S462G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768424:28768424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1145C>T |
| AA Mutation | p.Ala382Val(p.A382V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28767812:28767812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.533A>C |
| AA Mutation | p.Lys178Thr(p.K178T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768354:28768354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1075G>A |
| AA Mutation | p.Ala359Thr(p.A359T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768673:28768673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1394C>T |
| AA Mutation | p.Thr465Met(p.T465M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768427:28768427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1148C>T |
| AA Mutation | p.Ala383Val(p.A383V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313071 |
| Start | 28767903:28767903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267606826 |
| CDS Mutation | c.624C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |