Primary Site >> Stomach Cancer
Gene >> HS3ST1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002596 |
| Start | 11399467:11399467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.539G>C |
| AA Mutation | p.Arg180Pro(p.R180P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002596 |
| Start | 11399759:11399759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759091254 |
| CDS Mutation | c.247G>A |
| AA Mutation | p.Ala83Thr(p.A83T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002596 |
| Start | 11399779:11399779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.227T>C |
| AA Mutation | p.Leu76Pro(p.L76P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002596 |
| Start | 11399392:11399392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570976366 |
| CDS Mutation | c.614G>A |
| AA Mutation | p.Arg205His(p.R205H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002596 |
| Start | 11399464:11399464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.542A>G |
| AA Mutation | p.Asp181Gly(p.D181G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002596 |
| Start | 11399732:11399732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750639573 |
| CDS Mutation | c.274T>C |
| AA Mutation | p.Trp92Arg(p.W92R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002596 |
| Start | 11399936:11399936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369514297 |
| CDS Mutation | c.70G>A |
| AA Mutation | p.Glu24Lys(p.E24K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002596 |
| Start | 11399222:11399222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.784C>T |
| AA Mutation | p.Arg262Trp(p.R262W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000002596 |
| Start | 11399289:11399289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775585879 |
| CDS Mutation | c.717G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000002596 |
| Start | 11399274:11399274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745784456 |
| CDS Mutation | c.732G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000002596 |
| Start | 11399559:11399559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747203335 |
| CDS Mutation | c.447G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000002596 |
| Start | 11399187:11399187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759447246 |
| CDS Mutation | c.819G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000002596 |
| Start | 11399466:11399466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761018180 |
| CDS Mutation | c.540C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |