Primary Site >> Stomach Cancer
Gene >> HNF1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617811 |
| Start | 37731787:37731787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.853G>A |
| AA Mutation | p.Gly285Ser(p.G285S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617811 |
| Start | 37733723:37733723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.643G>C |
| AA Mutation | p.Gly215Arg(p.G215R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617811 |
| Start | 37739540:37739540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147218489 |
| CDS Mutation | c.444G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617811 |
| Start | 37705008:37705008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1248G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617811 |
| Start | 37699094:37699094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1635C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000617811 |
| Start | 37699168:37699168(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1561delC |
| AA Mutation | p.Gln521SerfsTer70(p.Q521Sfs*70) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant;start_lost |
| Transcription ID | ENST00000617811 |
| Start | 37744883:37744884(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1_2insCTTCCCATAATAAAAAAGTTCAAACAGACAAGGC |
| AA Mutation | p.Met1?(p.M1?) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000617811 |
| Start | 37744881:37744882(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3_4insTTT |
| AA Mutation | p.Met1_Val2insPhe(p.M1_V2insF) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |