Primary Site >> Stomach Cancer
Gene >> ST3GAL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399640 |
| Start | 133475783:133475783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.242C>A |
| AA Mutation | p.Thr81Asn(p.T81N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399640 |
| Start | 133464785:133464785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.676A>G |
| AA Mutation | p.Ile226Val(p.I226V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399640 |
| Start | 133476011:133476011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145602093 |
| CDS Mutation | c.14G>A |
| AA Mutation | p.Arg5Gln(p.R5Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399640 |
| Start | 133475813:133475813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.212C>T |
| AA Mutation | p.Ser71Leu(p.S71L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399640 |
| Start | 133461967:133461967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.757A>G |
| AA Mutation | p.Lys253Glu(p.K253E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399640 |
| Start | 133464915:133464915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.546G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399640 |
| Start | 133459848:133459848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200642820 |
| CDS Mutation | c.939G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |