Primary Site >> Stomach Cancer
Gene >> TERF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254942 |
| Start | 69366871:69366871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376057884 |
| CDS Mutation | c.1276G>A |
| AA Mutation | p.Ala426Thr(p.A426T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254942 |
| Start | 69370505:69370505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.818A>G |
| AA Mutation | p.Asp273Gly(p.D273G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254942 |
| Start | 69367192:69367192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762742087 |
| CDS Mutation | c.955C>T |
| AA Mutation | p.Arg319Trp(p.R319W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254942 |
| Start | 69368420:69368420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.903G>T |
| AA Mutation | p.Gln301His(p.Q301H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254942 |
| Start | 69356948:69356948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1579G>A |
| AA Mutation | p.Val527Met(p.V527M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254942 |
| Start | 69384611:69384611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.575T>A |
| AA Mutation | p.Val192Asp(p.V192D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000254942 |
| Start | 69357519:69357519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1469A>G |
| AA Mutation | p.Gln490Arg(p.Q490R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254942 |
| Start | 69368380:69368380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762832009 |
| CDS Mutation | c.943G>A |
| AA Mutation | p.Ala315Thr(p.A315T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254942 |
| Start | 69356986:69356986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1541C>T |
| AA Mutation | p.Ala514Val(p.A514V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254942 |
| Start | 69384610:69384610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761040166 |
| CDS Mutation | c.576C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |