Primary Site >> Stomach Cancer
Gene >> CYTIP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264192 |
| Start | 157415925:157415925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.832A>G |
| AA Mutation | p.Thr278Ala(p.T278A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264192 |
| Start | 157415931:157415931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756398323 |
| CDS Mutation | c.826C>T |
| AA Mutation | p.Arg276Trp(p.R276W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264192 |
| Start | 157415684:157415684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758705411 |
| CDS Mutation | c.1073G>A |
| AA Mutation | p.Arg358His(p.R358H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264192 |
| Start | 157443860:157443860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.161G>T |
| AA Mutation | p.Arg54Leu(p.R54L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264192 |
| Start | 157416027:157416027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748002457 |
| CDS Mutation | c.730A>C |
| AA Mutation | p.Ser244Arg(p.S244R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264192 |
| Start | 157430595:157430595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.440T>G |
| AA Mutation | p.Val147Gly(p.V147G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264192 |
| Start | 157415827:157415827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.930C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000264192 |
| Start | 157416042:157416042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371815413 |
| CDS Mutation | c.715C>T |
| AA Mutation | p.Arg239Ter(p.R239*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |