Primary Site >> Stomach Cancer
Gene >> ECM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369047 |
| Start | 150511047:150511047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.557A>C |
| AA Mutation | p.Gln186Pro(p.Q186P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000369047 |
| Start | 150512727:150512727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1307A>C |
| AA Mutation | p.Lys436Thr(p.K436T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369047 |
| Start | 150508268:150508268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.59C>T |
| AA Mutation | p.Ala20Val(p.A20V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369047 |
| Start | 150511043:150511043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150625690 |
| CDS Mutation | c.553C>T |
| AA Mutation | p.Arg185Cys(p.R185C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369047 |
| Start | 150510117:150510117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.320C>A |
| AA Mutation | p.Pro107His(p.P107H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369047 |
| Start | 150510929:150510929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.439G>T |
| AA Mutation | p.Ala147Ser(p.A147S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369047 |
| Start | 150512763:150512763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147907925 |
| CDS Mutation | c.1343G>A |
| AA Mutation | p.Arg448His(p.R448H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369047 |
| Start | 150513271:150513271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201023252 |
| CDS Mutation | c.1427G>A |
| AA Mutation | p.Arg476Gln(p.R476Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369047 |
| Start | 150512458:150512458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1190C>T |
| AA Mutation | p.Ala397Val(p.A397V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369047 |
| Start | 150511793:150511793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777173556 |
| CDS Mutation | c.1045T>C |
| AA Mutation | p.Cys349Arg(p.C349R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369047 |
| Start | 150511534:150511534(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.790delG |
| AA Mutation | p.Glu264ArgfsTer52(p.E264Rfs*52) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000369047 |
| Start | 150509696:150509696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121909115 |
| CDS Mutation | c.157C>T |
| AA Mutation | p.Arg53Ter(p.R53*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |