Primary Site >> Stomach Cancer
Gene >> HS3ST2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261374 |
| Start | 22915308:22915308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.850G>A |
| AA Mutation | p.Glu284Lys(p.E284K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261374 |
| Start | 22915300:22915300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.842C>T |
| AA Mutation | p.Pro281Leu(p.P281L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261374 |
| Start | 22915218:22915218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.760G>A |
| AA Mutation | p.Val254Met(p.V254M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261374 |
| Start | 22915132:22915132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.674T>A |
| AA Mutation | p.Ile225Asn(p.I225N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261374 |
| Start | 22814753:22814753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.143G>A |
| AA Mutation | p.Arg48His(p.R48H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261374 |
| Start | 22915087:22915087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746835350 |
| CDS Mutation | c.629G>A |
| AA Mutation | p.Arg210His(p.R210H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261374 |
| Start | 22915062:22915062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.604G>A |
| AA Mutation | p.Val202Met(p.V202M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261374 |
| Start | 22814660:22814660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.50C>T |
| AA Mutation | p.Ala17Val(p.A17V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261374 |
| Start | 22915204:22915204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.746G>A |
| AA Mutation | p.Arg249His(p.R249H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261374 |
| Start | 22915271:22915271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144169281 |
| CDS Mutation | c.813C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261374 |
| Start | 22915139:22915139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.681C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261374 |
| Start | 22915457:22915457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763351541 |
| CDS Mutation | c.999T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |