Primary Site >> Stomach Cancer
Gene >> DSPP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282478 |
| Start | 87612515:87612515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.329A>T |
| AA Mutation | p.Asn110Ile(p.N110I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282478 |
| Start | 87613148:87613148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.962A>C |
| AA Mutation | p.Lys321Thr(p.K321T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282478 |
| Start | 87612393:87612393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.207A>C |
| AA Mutation | p.Gln69His(p.Q69H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282478 |
| Start | 87612670:87612670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.484A>G |
| AA Mutation | p.Thr162Ala(p.T162A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282478 |
| Start | 87612443:87612443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.257C>A |
| AA Mutation | p.Ala86Glu(p.A86E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282478 |
| Start | 87612666:87612666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.480G>T |
| AA Mutation | p.Lys160Asn(p.K160N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282478 |
| Start | 87612584:87612584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.398C>T |
| AA Mutation | p.Ala133Val(p.A133V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282478 |
| Start | 87614269:87614269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1607A>G |
| AA Mutation | p.Asp536Gly(p.D536G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282478 |
| Start | 87612128:87612128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749329988 |
| CDS Mutation | c.75G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282478 |
| Start | 87614147:87614147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1485T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282478 |
| Start | 87612912:87612912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376633615 |
| CDS Mutation | c.726C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |