Primary Site >> Stomach Cancer
Gene >> NFIC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000443272 |
| Start | 3381904:3381904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751328600 |
| CDS Mutation | c.223C>T |
| AA Mutation | p.Arg75Trp(p.R75W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000443272 |
| Start | 3381934:3381934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.253C>T |
| AA Mutation | p.Arg85Trp(p.R85W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000443272 |
| Start | 3452581:3452581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140170107 |
| CDS Mutation | c.1184G>A |
| AA Mutation | p.Arg395His(p.R395H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000443272 |
| Start | 3382067:3382067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.386G>A |
| AA Mutation | p.Arg129Gln(p.R129Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000443272 |
| Start | 3433545:3433545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.662T>C |
| AA Mutation | p.Val221Ala(p.V221A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000443272 |
| Start | 3452529:3452529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1132A>G |
| AA Mutation | p.Thr378Ala(p.T378A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000443272 |
| Start | 3452548:3452548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374896582 |
| CDS Mutation | c.1151C>T |
| AA Mutation | p.Thr384Met(p.T384M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000443272 |
| Start | 3382068:3382068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.387G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000443272 |
| Start | 3433555:3433555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762649968 |
| CDS Mutation | c.672C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |