Primary Site >> Stomach Cancer
Gene >> TYRO3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263798 |
| Start | 41567424:41567424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.848G>A |
| AA Mutation | p.Cys283Tyr(p.C283Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000263798 |
| Start | 41571118:41571118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1660G>T |
| AA Mutation | p.Ala554Ser(p.A554S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263798 |
| Start | 41577955:41577955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2352G>T |
| AA Mutation | p.Met784Ile(p.M784I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263798 |
| Start | 41577932:41577932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2329C>G |
| AA Mutation | p.Pro777Ala(p.P777A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263798 |
| Start | 41573688:41573688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748781112 |
| CDS Mutation | c.2155G>A |
| AA Mutation | p.Gly719Arg(p.G719R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263798 |
| Start | 41578089:41578089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2486G>A |
| AA Mutation | p.Ser829Asn(p.S829N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263798 |
| Start | 41572476:41572476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1787T>G |
| AA Mutation | p.Leu596Arg(p.L596R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263798 |
| Start | 41573781:41573781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145529129 |
| CDS Mutation | c.2248C>T |
| AA Mutation | p.Arg750Cys(p.R750C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263798 |
| Start | 41572458:41572458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1769G>A |
| AA Mutation | p.Ser590Asn(p.S590N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263798 |
| Start | 41578227:41578227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2624A>G |
| AA Mutation | p.Gln875Arg(p.Q875R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263798 |
| Start | 41572537:41572537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377341711 |
| CDS Mutation | c.1848C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |