Primary Site >> Pancreatic Cancer
Gene >> MYH7B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262873 |
| Start | 34978040:34978040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.161G>A |
| AA Mutation | p.Arg54His(p.R54H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262873 |
| Start | 34979707:34979707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539864476 |
| CDS Mutation | c.371G>A |
| AA Mutation | p.Arg124His(p.R124H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262873 |
| Start | 34987894:34987894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376103118 |
| CDS Mutation | c.1522G>A |
| AA Mutation | p.Ala508Thr(p.A508T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262873 |
| Start | 34989801:34989801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1775G>T |
| AA Mutation | p.Ser592Ile(p.S592I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262873 |
| Start | 34990801:34990801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2167G>A |
| AA Mutation | p.Val723Ile(p.V723I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262873 |
| Start | 34991076:34991076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2264G>A |
| AA Mutation | p.Arg755His(p.R755H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262873 |
| Start | 35000295:35000295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770125496 |
| CDS Mutation | c.4910G>A |
| AA Mutation | p.Arg1637His(p.R1637H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262873 |
| Start | 34998408:34998409(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3988_3989delCA |
| AA Mutation | p.Gln1330AspfsTer60(p.Q1330Dfs*60) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262873 |
| Start | 35001041:35001041(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5485delG |
| AA Mutation | p.Glu1829AsnfsTer3(p.E1829Nfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |