Primary Site >> Stomach Cancer
Gene >> GPR32
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270590 |
| Start | 50770812:50770812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.212G>A |
| AA Mutation | p.Arg71His(p.R71H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270590 |
| Start | 50771593:50771593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.993G>C |
| AA Mutation | p.Leu331Phe(p.L331F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270590 |
| Start | 50771508:50771508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.908C>T |
| AA Mutation | p.Ala303Val(p.A303V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270590 |
| Start | 50771648:50771648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755214712 |
| CDS Mutation | c.1048C>T |
| AA Mutation | p.Arg350Cys(p.R350C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270590 |
| Start | 50770662:50770662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.62G>A |
| AA Mutation | p.Arg21His(p.R21H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270590 |
| Start | 50771084:50771084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.484G>C |
| AA Mutation | p.Ala162Pro(p.A162P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000270590 |
| Start | 50770615:50770615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756485883 |
| CDS Mutation | c.15G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000270590 |
| Start | 50771125:50771125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768827782 |
| CDS Mutation | c.525G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000270590 |
| Start | 50771413:50771413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.813G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000270590 |
| Start | 50771548:50771548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765329940 |
| CDS Mutation | c.948C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |