Primary Site >> Stomach Cancer
Gene >> GHSR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241256 |
| Start | 172447879:172447879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.535T>A |
| AA Mutation | p.Phe179Ile(p.F179I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241256 |
| Start | 172447728:172447728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200804910 |
| CDS Mutation | c.686C>T |
| AA Mutation | p.Thr229Met(p.T229M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241256 |
| Start | 172447779:172447779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.635T>C |
| AA Mutation | p.Val212Ala(p.V212A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241256 |
| Start | 172448200:172448200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.214C>T |
| AA Mutation | p.Arg72Cys(p.R72C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241256 |
| Start | 172445360:172445360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.902G>A |
| AA Mutation | p.Ser301Asn(p.S301N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241256 |
| Start | 172447798:172447798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.616C>T |
| AA Mutation | p.Arg206Cys(p.R206C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241256 |
| Start | 172445196:172445196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1066T>C |
| AA Mutation | p.Ser356Pro(p.S356P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241256 |
| Start | 172448265:172448265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.149G>A |
| AA Mutation | p.Cys50Tyr(p.C50Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241256 |
| Start | 172448014:172448014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.400A>T |
| AA Mutation | p.Ile134Phe(p.I134F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241256 |
| Start | 172448404:172448404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10G>A |
| AA Mutation | p.Ala4Thr(p.A4T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241256 |
| Start | 172447856:172447856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.558C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241256 |
| Start | 172448399:172448399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241256 |
| Start | 172448297:172448297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776496820 |
| CDS Mutation | c.117C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241256 |
| Start | 172448318:172448318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751202593 |
| CDS Mutation | c.96C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241256 |
| Start | 172448234:172448234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753808890 |
| CDS Mutation | c.180C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |