Primary Site >> Stomach Cancer
Gene >> CRNN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271835 |
| Start | 152410363:152410363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.719A>G |
| AA Mutation | p.Gln240Arg(p.Q240R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271835 |
| Start | 152409812:152409812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1270C>T |
| AA Mutation | p.Arg424Cys(p.R424C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271835 |
| Start | 152410800:152410800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.282G>T |
| AA Mutation | p.Glu94Asp(p.E94D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271835 |
| Start | 152409946:152409946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376325882 |
| CDS Mutation | c.1136C>T |
| AA Mutation | p.Thr379Met(p.T379M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271835 |
| Start | 152410238:152410238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.844G>T |
| AA Mutation | p.Val282Leu(p.V282L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271835 |
| Start | 152410162:152410162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.920G>A |
| AA Mutation | p.Ser307Asn(p.S307N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271835 |
| Start | 152410200:152410200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.882C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271835 |
| Start | 152410089:152410089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760762248 |
| CDS Mutation | c.993C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |