Primary Site >> Stomach Cancer
Gene >> ADGRG1
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000567835 |
| Start | 57655991:57655991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs575505827 |
| CDS Mutation | c.1016C>T |
| AA Mutation | p.Pro339Leu(p.P339L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000567835 |
| Start | 57661812:57661812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371152613 |
| CDS Mutation | c.1798C>T |
| AA Mutation | p.Arg600Cys(p.R600C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000567835 |
| Start | 57655460:57655460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546067405 |
| CDS Mutation | c.830C>T |
| AA Mutation | p.Thr277Met(p.T277M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000567835 |
| Start | 57651298:57651298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770388074 |
| CDS Mutation | c.163C>T |
| AA Mutation | p.Arg55Cys(p.R55C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000567835 |
| Start | 57661902:57661902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1888T>A |
| AA Mutation | p.Phe630Ile(p.F630I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000567835 |
| Start | 57651477:57651477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.342C>A |
| AA Mutation | p.Asp114Glu(p.D114E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000567835 |
| Start | 57656555:57656555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs541949258 |
| CDS Mutation | c.1105G>A |
| AA Mutation | p.Val369Ile(p.V369I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000567835 |
| Start | 57659567:57659567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1459C>A |
| AA Mutation | p.Leu487Ile(p.L487I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000567835 |
| Start | 57650314:57650314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142223451 |
| CDS Mutation | c.27G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000567835 |
| Start | 57654088:57654088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.723G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000567835 |
| Start | 57661928:57661928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748659368 |
| CDS Mutation | c.1914C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000567835 |
| Start | 57657393:57657393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368883473 |
| CDS Mutation | c.1188C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000567835 |
| Start | 57655473:57655473(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.843delC |
| AA Mutation | p.Ser281ArgfsTer42(p.S281Rfs*42) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000567835 |
| Start | 57663451:57663451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1952-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |