Primary Site >> Stomach Cancer
Gene >> CHD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394196 |
| Start | 92939694:92939694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.668G>A |
| AA Mutation | p.Arg223His(p.R223H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394196 |
| Start | 93024650:93024650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5432G>A |
| AA Mutation | p.Arg1811Lys(p.R1811K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394196 |
| Start | 92939675:92939675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.649G>A |
| AA Mutation | p.Ala217Thr(p.A217T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394196 |
| Start | 93004690:93004690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4352G>A |
| AA Mutation | p.Ser1451Asn(p.S1451N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394196 |
| Start | 92939697:92939697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770105179 |
| CDS Mutation | c.671G>A |
| AA Mutation | p.Arg224Gln(p.R224Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394196 |
| Start | 92981368:92981368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2977A>G |
| AA Mutation | p.Met993Val(p.M993V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394196 |
| Start | 93020074:93020074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4969T>C |
| AA Mutation | p.Trp1657Arg(p.W1657R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394196 |
| Start | 92924449:92924449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759974626 |
| CDS Mutation | c.191C>T |
| AA Mutation | p.Ser64Leu(p.S64L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394196 |
| Start | 93024695:93024695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5477G>A |
| AA Mutation | p.Arg1826Gln(p.R1826Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394196 |
| Start | 93014713:93014713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4710C>G |
| AA Mutation | p.Asp1570Glu(p.D1570E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394196 |
| Start | 92984470:92984470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3207G>A |
| AA Mutation | p.Met1069Ile(p.M1069I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394196 |
| Start | 92997348:92997348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3830G>A |
| AA Mutation | p.Gly1277Asp(p.G1277D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394196 |
| Start | 93009165:93009165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199572989 |
| CDS Mutation | c.4434C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394196 |
| Start | 92985569:92985569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3309T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394196 |
| Start | 92978362:92978362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759185042 |
| CDS Mutation | c.2706T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394196 |
| Start | 92985620:92985620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3360G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394196 |
| Start | 92946141:92946141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765523530 |
| CDS Mutation | c.1302A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394196 |
| Start | 92937589:92937589(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs748694853 |
| CDS Mutation | c.522delA |
| AA Mutation | p.Val175Ter(p.V175*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394196 |
| Start | 92997299:92997300(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3787dupG |
| AA Mutation | p.Val1263GlyfsTer4(p.V1263Gfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |