Primary Site >> Stomach Cancer
Gene >> SSTR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267377 |
| Start | 38210207:38210207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.818T>C |
| AA Mutation | p.Val273Ala(p.V273A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267377 |
| Start | 38209525:38209525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777857855 |
| CDS Mutation | c.136T>C |
| AA Mutation | p.Ser46Pro(p.S46P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267377 |
| Start | 38209645:38209645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.256T>A |
| AA Mutation | p.Tyr86Asn(p.Y86N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267377 |
| Start | 38210072:38210072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.683T>C |
| AA Mutation | p.Phe228Ser(p.F228S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267377 |
| Start | 38209643:38209643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.254G>A |
| AA Mutation | p.Arg85His(p.R85H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267377 |
| Start | 38209883:38209883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749677430 |
| CDS Mutation | c.494C>T |
| AA Mutation | p.Ala165Val(p.A165V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267377 |
| Start | 38209805:38209805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.416T>G |
| AA Mutation | p.Val139Gly(p.V139G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267377 |
| Start | 38210396:38210396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1007G>A |
| AA Mutation | p.Arg336His(p.R336H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267377 |
| Start | 38209769:38209769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.380C>T |
| AA Mutation | p.Ala127Val(p.A127V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267377 |
| Start | 38210313:38210313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.924G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267377 |
| Start | 38210457:38210457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756715931 |
| CDS Mutation | c.1068C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |