Primary Site >> Stomach Cancer
Gene >> GRN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000053867 |
| Start | 44351742:44351742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143030899 |
| CDS Mutation | c.1126G>A |
| AA Mutation | p.Asp376Asn(p.D376N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000053867 |
| Start | 44350772:44350772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.680G>A |
| AA Mutation | p.Gly227Glu(p.G227E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000053867 |
| Start | 44349267:44349267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533451404 |
| CDS Mutation | c.103G>A |
| AA Mutation | p.Gly35Arg(p.G35R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000053867 |
| Start | 44349291:44349291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.127C>T |
| AA Mutation | p.Arg43Cys(p.R43C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000053867 |
| Start | 44350311:44350311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.433G>T |
| AA Mutation | p.Gly145Cys(p.G145C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000053867 |
| Start | 44352737:44352737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756117423 |
| CDS Mutation | c.1721G>A |
| AA Mutation | p.Arg574His(p.R574H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000053867 |
| Start | 44352711:44352711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs63751248 |
| CDS Mutation | c.1695C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000053867 |
| Start | 44350280:44350280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201932427 |
| CDS Mutation | c.402G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000053867 |
| Start | 44352382:44352382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1455C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000053867 |
| Start | 44349515:44349515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144736470 |
| CDS Mutation | c.228C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000053867 |
| Start | 44352723:44352723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1707T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000053867 |
| Start | 44350707:44350707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372963871 |
| CDS Mutation | c.615G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000053867 |
| Start | 44350233:44350233(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.356delA |
| AA Mutation | p.Asn119ThrfsTer137(p.N119Tfs*137) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |