Primary Site >> Stomach Cancer
Gene >> STMN4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265770 |
| Start | 27241227:27241227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.145G>A |
| AA Mutation | p.Asp49Asn(p.D49N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265770 |
| Start | 27241218:27241218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.154G>A |
| AA Mutation | p.Val52Ile(p.V52I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265770 |
| Start | 27240146:27240146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.335T>C |
| AA Mutation | p.Leu112Pro(p.L112P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265770 |
| Start | 27239985:27239985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764508091 |
| CDS Mutation | c.496C>T |
| AA Mutation | p.Arg166Trp(p.R166W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265770 |
| Start | 27240152:27240152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755190482 |
| CDS Mutation | c.329C>T |
| AA Mutation | p.Ala110Val(p.A110V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265770 |
| Start | 27236894:27236894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs73563904 |
| CDS Mutation | c.522C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |