Primary Site >> Stomach Cancer
Gene >> C1S
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328916 |
| Start | 7070325:7070325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373197181 |
| CDS Mutation | c.1741C>T |
| AA Mutation | p.Arg581Cys(p.R581C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328916 |
| Start | 7065238:7065238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147341600 |
| CDS Mutation | c.656G>A |
| AA Mutation | p.Arg219Gln(p.R219Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328916 |
| Start | 7070217:7070217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782412161 |
| CDS Mutation | c.1633G>A |
| AA Mutation | p.Val545Ile(p.V545I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328916 |
| Start | 7070197:7070197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1613C>G |
| AA Mutation | p.Pro538Arg(p.P538R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328916 |
| Start | 7070335:7070335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782616996 |
| CDS Mutation | c.1751C>T |
| AA Mutation | p.Ala584Val(p.A584V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328916 |
| Start | 7070043:7070043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1459G>A |
| AA Mutation | p.Val487Ile(p.V487I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328916 |
| Start | 7070574:7070574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1990C>G |
| AA Mutation | p.Leu664Val(p.L664V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328916 |
| Start | 7069972:7069972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375077429 |
| CDS Mutation | c.1388C>T |
| AA Mutation | p.Ala463Val(p.A463V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328916 |
| Start | 7070510:7070510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1926T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000328916 |
| Start | 7065935:7065935(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs781818365 |
| CDS Mutation | c.842delA |
| AA Mutation | p.Lys281ArgfsTer39(p.K281Rfs*39) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |