Primary Site >> Stomach Cancer
Gene >> PELP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000574876 |
| Start | 4691399:4691399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377024175 |
| CDS Mutation | c.293G>A |
| AA Mutation | p.Arg98His(p.R98H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000574876 |
| Start | 4682544:4682544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.600G>T |
| AA Mutation | p.Lys200Asn(p.K200N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000574876 |
| Start | 4672901:4672901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs558960670 |
| CDS Mutation | c.2090C>T |
| AA Mutation | p.Ser697Leu(p.S697L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000574876 |
| Start | 4675154:4675154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749311186 |
| CDS Mutation | c.1199G>A |
| AA Mutation | p.Arg400His(p.R400H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000574876 |
| Start | 4672962:4672962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2029A>G |
| AA Mutation | p.Met677Val(p.M677V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000574876 |
| Start | 4672022:4672022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2969A>T |
| AA Mutation | p.Glu990Val(p.E990V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000574876 |
| Start | 4690921:4690921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.387G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000574876 |
| Start | 4672999:4672999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1992G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000574876 |
| Start | 4671895:4671895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3096C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000574876 |
| Start | 4671901:4671901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370860807 |
| CDS Mutation | c.3090G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000574876 |
| Start | 4671692:4671692(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3299delA |
| AA Mutation | p.Lys1100ArgfsTer43(p.K1100Rfs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |