Primary Site >> Stomach Cancer
Gene >> STRADA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336174 |
| Start | 63710833:63710833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755408458 |
| CDS Mutation | c.352G>A |
| AA Mutation | p.Glu118Lys(p.E118K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336174 |
| Start | 63704357:63704357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764311000 |
| CDS Mutation | c.1084C>T |
| AA Mutation | p.Arg362Cys(p.R362C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336174 |
| Start | 63703614:63703614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758494527 |
| CDS Mutation | c.1281C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336174 |
| Start | 63704448:63704448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.993C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336174 |
| Start | 63710795:63710795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764868771 |
| CDS Mutation | c.390C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336174 |
| Start | 63726684:63726684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530585509 |
| CDS Mutation | c.48G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336174 |
| Start | 63704562:63704562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147552949 |
| CDS Mutation | c.879C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000336174 |
| Start | 63704043:63704044(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1104_1105delCA |
| AA Mutation | p.Ser369CysfsTer35(p.S369Cfs*35) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000336174 |
| Start | 63703698:63703698(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1197delC |
| AA Mutation | p.Ile400SerfsTer19(p.I400Sfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000336174 |
| Start | 63704444:63704444(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs762120842 |
| CDS Mutation | c.997delC |
| AA Mutation | p.Arg333GlyfsTer42(p.R333Gfs*42) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |