Primary Site >> Esophagus Cancer
Gene >> MMS22L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275053 |
| Start | 97149871:97149871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3632G>A |
| AA Mutation | p.Gly1211Asp(p.G1211D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275053 |
| Start | 97162040:97162040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3347G>C |
| AA Mutation | p.Gly1116Ala(p.G1116A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275053 |
| Start | 97263370:97263370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.907C>A |
| AA Mutation | p.Leu303Ile(p.L303I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275053 |
| Start | 97231558:97231558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1397G>C |
| AA Mutation | p.Cys466Ser(p.C466S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000275053 |
| Start | 97151867:97151867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3386T>A |
| AA Mutation | p.Val1129Asp(p.V1129D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275053 |
| Start | 97165308:97165308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3159G>C |
| AA Mutation | p.Leu1053Phe(p.L1053F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275053 |
| Start | 97228950:97228950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1983A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |