Primary Site >> Stomach Cancer
Gene >> HEY2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368364 |
| Start | 125754525:125754525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.307C>T |
| AA Mutation | p.Leu103Phe(p.L103F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368364 |
| Start | 125759522:125759522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.734G>A |
| AA Mutation | p.Ser245Asn(p.S245N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368364 |
| Start | 125759192:125759192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.404G>A |
| AA Mutation | p.Arg135Gln(p.R135Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368364 |
| Start | 125759455:125759455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.667G>A |
| AA Mutation | p.Gly223Ser(p.G223S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368364 |
| Start | 125759778:125759778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.990G>T |
| AA Mutation | p.Trp330Cys(p.W330C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368364 |
| Start | 125759703:125759703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756533636 |
| CDS Mutation | c.915G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368364 |
| Start | 125759634:125759634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763500780 |
| CDS Mutation | c.846C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368364 |
| Start | 125759685:125759685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.897G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368364 |
| Start | 125759592:125759592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.804C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368364 |
| Start | 125759607:125759607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs34745209 |
| CDS Mutation | c.819G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368364 |
| Start | 125759656:125759656(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.872delC |
| AA Mutation | p.Pro291GlnfsTer56(p.P291Qfs*56) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368364 |
| Start | 125752083:125752083(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.243delA |
| AA Mutation | p.Lys81AsnfsTer7(p.K81Nfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |