Primary Site >> Stomach Cancer
Gene >> NR1I2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393716 |
| Start | 119810110:119810110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.247G>A |
| AA Mutation | p.Ala83Thr(p.A83T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393716 |
| Start | 119807360:119807360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.110G>A |
| AA Mutation | p.Gly37Asp(p.G37D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393716 |
| Start | 119812894:119812894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.728T>C |
| AA Mutation | p.Met243Thr(p.M243T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393716 |
| Start | 119815020:119815020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.836C>G |
| AA Mutation | p.Ala279Gly(p.A279G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393716 |
| Start | 119815064:119815064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763780333 |
| CDS Mutation | c.880G>A |
| AA Mutation | p.Ala294Thr(p.A294T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393716 |
| Start | 119815752:119815752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780684359 |
| CDS Mutation | c.1081G>A |
| AA Mutation | p.Val361Met(p.V361M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393716 |
| Start | 119812708:119812708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.542G>A |
| AA Mutation | p.Gly181Asp(p.G181D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393716 |
| Start | 119815427:119815427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1042C>A |
| AA Mutation | p.Leu348Ile(p.L348I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393716 |
| Start | 119807340:119807340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201105889 |
| CDS Mutation | c.90C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393716 |
| Start | 119815778:119815778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369188703 |
| CDS Mutation | c.1107C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |