Primary Site >> Stomach Cancer
Gene >> ADGRE2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315576 |
| Start | 14764592:14764592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.925G>A |
| AA Mutation | p.Asp309Asn(p.D309N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315576 |
| Start | 14772473:14772473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754889485 |
| CDS Mutation | c.224C>T |
| AA Mutation | p.Ser75Leu(p.S75L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315576 |
| Start | 14765356:14765356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.870A>C |
| AA Mutation | p.Arg290Ser(p.R290S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315576 |
| Start | 14743767:14743767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs564713952 |
| CDS Mutation | c.2201C>T |
| AA Mutation | p.Ala734Val(p.A734V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315576 |
| Start | 14754964:14754964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1580A>G |
| AA Mutation | p.Tyr527Cys(p.Y527C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315576 |
| Start | 14774012:14774012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.125C>T |
| AA Mutation | p.Ala42Val(p.A42V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315576 |
| Start | 14751553:14751553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1907A>G |
| AA Mutation | p.Tyr636Cys(p.Y636C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315576 |
| Start | 14746241:14746241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374432034 |
| CDS Mutation | c.2174G>A |
| AA Mutation | p.Arg725Gln(p.R725Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000315576 |
| Start | 14752330:14752330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1787A>C |
| AA Mutation | p.Lys596Thr(p.K596T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315576 |
| Start | 14772472:14772472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.225G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315576 |
| Start | 14751642:14751642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1818G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315576 |
| Start | 14743625:14743625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2343C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315576 |
| Start | 14766362:14766362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748645336 |
| CDS Mutation | c.507C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |