Primary Site >> Stomach Cancer
Gene >> HMMR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358715 |
| Start | 163482712:163482712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1453G>A |
| AA Mutation | p.Ala485Thr(p.A485T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358715 |
| Start | 163473192:163473192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.661A>G |
| AA Mutation | p.Lys221Glu(p.K221E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358715 |
| Start | 163473444:163473444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.788A>C |
| AA Mutation | p.Glu263Ala(p.E263A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358715 |
| Start | 163475485:163475485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1078C>T |
| AA Mutation | p.Leu360Phe(p.L360F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358715 |
| Start | 163483324:163483324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759515223 |
| CDS Mutation | c.1739G>A |
| AA Mutation | p.Arg580His(p.R580H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358715 |
| Start | 163474191:163474191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1036C>A |
| AA Mutation | p.Leu346Met(p.L346M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358715 |
| Start | 163471448:163471448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777211342 |
| CDS Mutation | c.632A>G |
| AA Mutation | p.Gln211Arg(p.Q211R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358715 |
| Start | 163483323:163483323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140371330 |
| CDS Mutation | c.1738C>T |
| AA Mutation | p.Arg580Cys(p.R580C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358715 |
| Start | 163490420:163490420(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs761272507 |
| CDS Mutation | c.1998delA |
| AA Mutation | p.Lys666AsnfsTer11(p.K666Nfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |