Primary Site >> Stomach Cancer
Gene >> HRC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252825 |
| Start | 49154156:49154156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759163594 |
| CDS Mutation | c.1082G>A |
| AA Mutation | p.Arg361His(p.R361H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252825 |
| Start | 49154933:49154933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.305T>C |
| AA Mutation | p.Leu102Pro(p.L102P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252825 |
| Start | 49153523:49153523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1715A>G |
| AA Mutation | p.Glu572Gly(p.E572G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252825 |
| Start | 49154968:49154968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.270G>T |
| AA Mutation | p.Lys90Asn(p.K90N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252825 |
| Start | 49152046:49152046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1984T>C |
| AA Mutation | p.Cys662Arg(p.C662R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252825 |
| Start | 49154965:49154965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.273G>T |
| AA Mutation | p.Glu91Asp(p.E91D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252825 |
| Start | 49154575:49154575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.663T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252825 |
| Start | 49153420:49153420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs190856179 |
| CDS Mutation | c.1818C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |