Primary Site >> Stomach Cancer
Gene >> PCDHGA9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000573521 |
| Start | 141404930:141404930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752075185 |
| CDS Mutation | c.1978C>T |
| AA Mutation | p.Leu660Phe(p.L660F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000573521 |
| Start | 141403586:141403586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.634C>A |
| AA Mutation | p.Leu212Ile(p.L212I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000573521 |
| Start | 141403167:141403167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.215C>T |
| AA Mutation | p.Thr72Met(p.T72M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000573521 |
| Start | 141404073:141404073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746951310 |
| CDS Mutation | c.1121G>A |
| AA Mutation | p.Arg374Gln(p.R374Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000573521 |
| Start | 141404862:141404862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377687399 |
| CDS Mutation | c.1910C>T |
| AA Mutation | p.Ala637Val(p.A637V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000573521 |
| Start | 141403166:141403166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.214A>G |
| AA Mutation | p.Thr72Ala(p.T72A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000573521 |
| Start | 141403302:141403302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.350A>G |
| AA Mutation | p.Tyr117Cys(p.Y117C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000573521 |
| Start | 141403596:141403596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.644C>T |
| AA Mutation | p.Ser215Leu(p.S215L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000573521 |
| Start | 141404645:141404645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1693C>T |
| AA Mutation | p.Pro565Ser(p.P565S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000573521 |
| Start | 141403261:141403261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.309G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000573521 |
| Start | 141403357:141403357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.405C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000573521 |
| Start | 141403441:141403441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.489C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000573521 |
| Start | 141403168:141403168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.216G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000573521 |
| Start | 141404347:141404347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1395C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000573521 |
| Start | 141405118:141405118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368800698 |
| CDS Mutation | c.2166G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |