Primary Site >> Stomach Cancer
Gene >> ESRP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433389 |
| Start | 94678218:94678218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1667C>T |
| AA Mutation | p.Ser556Phe(p.S556F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433389 |
| Start | 94668003:94668003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.986G>A |
| AA Mutation | p.Arg329His(p.R329H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433389 |
| Start | 94641389:94641389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.71G>C |
| AA Mutation | p.Gly24Ala(p.G24A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000433389 |
| Start | 94646282:94646282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.490T>C |
| AA Mutation | p.Tyr164His(p.Y164H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433389 |
| Start | 94668174:94668174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1157C>T |
| AA Mutation | p.Ala386Val(p.A386V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000433389 |
| Start | 94692826:94692826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1970A>T |
| AA Mutation | p.Gln657Leu(p.Q657L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433389 |
| Start | 94678323:94678323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1772A>G |
| AA Mutation | p.Tyr591Cys(p.Y591C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433389 |
| Start | 94678259:94678259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1708G>A |
| AA Mutation | p.Ala570Thr(p.A570T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433389 |
| Start | 94668134:94668134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1117G>A |
| AA Mutation | p.Ala373Thr(p.A373T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000433389 |
| Start | 94678264:94678264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1713C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000433389 |
| Start | 94646263:94646263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376259698 |
| CDS Mutation | c.471C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000433389 |
| Start | 94674383:94674383(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs775950025 |
| CDS Mutation | c.1535delA |
| AA Mutation | p.Asn512ThrfsTer2(p.N512Tfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000433389 |
| Start | 94671613:94671614(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1399dupG |
| AA Mutation | p.Glu467GlyfsTer44(p.E467Gfs*44) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | splice_donor_variant;intron_variant |
| Transcription ID | ENST00000433389 |
| Start | 94692828:94692831(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1971+3_1971+6delCAGT |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |