Primary Site >> Stomach Cancer
Gene >> TCF7L2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355995 |
| Start | 113152427:113152427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1256C>T |
| AA Mutation | p.Ala419Val(p.A419V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355995 |
| Start | 113144007:113144007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.770T>G |
| AA Mutation | p.Leu257Arg(p.L257R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355995 |
| Start | 113040104:113040104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.530C>A |
| AA Mutation | p.Ser177Tyr(p.S177Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355995 |
| Start | 113165574:113165574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1462C>T |
| AA Mutation | p.Arg488Cys(p.R488C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355995 |
| Start | 113146037:113146037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.815C>T |
| AA Mutation | p.Thr272Met(p.T272M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355995 |
| Start | 113159947:113159947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1397C>T |
| AA Mutation | p.Ala466Val(p.A466V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355995 |
| Start | 113165571:113165571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368331428 |
| CDS Mutation | c.1459G>A |
| AA Mutation | p.Val487Ile(p.V487I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355995 |
| Start | 112950896:112950896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.140C>T |
| AA Mutation | p.Ser47Phe(p.S47F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355995 |
| Start | 112964599:112964599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200865074 |
| CDS Mutation | c.425C>T |
| AA Mutation | p.Thr142Met(p.T142M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355995 |
| Start | 113151805:113151805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1082T>G |
| AA Mutation | p.Met361Arg(p.M361R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355995 |
| Start | 113165742:113165742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758342453 |
| CDS Mutation | c.1630G>A |
| AA Mutation | p.Ala544Thr(p.A544T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355995 |
| Start | 113152429:113152429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1258C>T |
| AA Mutation | p.Arg420Trp(p.R420W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355995 |
| Start | 113165570:113165570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780509521 |
| CDS Mutation | c.1458C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355995 |
| Start | 113165807:113165807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761028094 |
| CDS Mutation | c.1695C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355995 |
| Start | 113141234:113141234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750351798 |
| CDS Mutation | c.603G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355995 |
| Start | 113151827:113151827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1104C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355995 |
| Start | 113165948:113165948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1836G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355995 |
| Start | 113165643:113165643(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs768101780 |
| CDS Mutation | c.1536delC |
| AA Mutation | p.Ser513ProfsTer5(p.S513Pfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355995 |
| Start | 113165863:113165863(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1755delC |
| AA Mutation | p.Ser586ProfsTer33(p.S586Pfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |