Primary Site >> Stomach Cancer
Gene >> MSLN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382862 |
| Start | 766414:766414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150147307 |
| CDS Mutation | c.1154G>A |
| AA Mutation | p.Arg385His(p.R385H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382862 |
| Start | 766088:766088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760725450 |
| CDS Mutation | c.925C>T |
| AA Mutation | p.Arg309Cys(p.R309C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382862 |
| Start | 765535:765535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764327536 |
| CDS Mutation | c.713C>T |
| AA Mutation | p.Ser238Leu(p.S238L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382862 |
| Start | 766131:766131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.968T>C |
| AA Mutation | p.Leu323Pro(p.L323P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382862 |
| Start | 767420:767420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1570G>A |
| AA Mutation | p.Val524Met(p.V524M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382862 |
| Start | 765589:765589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.767G>C |
| AA Mutation | p.Gly256Ala(p.G256A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382862 |
| Start | 766649:766649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1236T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382862 |
| Start | 767404:767404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371328406 |
| CDS Mutation | c.1554G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382862 |
| Start | 765536:765536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774690027 |
| CDS Mutation | c.714G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000382862 |
| Start | 765527:765527(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.710delC |
| AA Mutation | p.Pro237ArgfsTer75(p.P237Rfs*75) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382862 |
| Start | 766794:766794(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs780605061 |
| CDS Mutation | c.1386delC |
| AA Mutation | p.Ser463AlafsTer33(p.S463Afs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |