Primary Site >> Stomach Cancer
Gene >> PUF60
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000526683 |
| Start | 143817638:143817638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.962C>T |
| AA Mutation | p.Ala321Val(p.A321V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000526683 |
| Start | 143820683:143820683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.331C>T |
| AA Mutation | p.Leu111Phe(p.L111F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000526683 |
| Start | 143816714:143816714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1486G>A |
| AA Mutation | p.Val496Ile(p.V496I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000526683 |
| Start | 143817662:143817662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.938C>T |
| AA Mutation | p.Ala313Val(p.A313V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000526683 |
| Start | 143820713:143820713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.301G>A |
| AA Mutation | p.Ala101Thr(p.A101T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000526683 |
| Start | 143816717:143816717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1483C>A |
| AA Mutation | p.Arg495Ser(p.R495S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000526683 |
| Start | 143818464:143818464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.419T>C |
| AA Mutation | p.Leu140Pro(p.L140P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000526683 |
| Start | 143817992:143817992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764497081 |
| CDS Mutation | c.687C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000526683 |
| Start | 143817947:143817947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373238114 |
| CDS Mutation | c.732C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000526683 |
| Start | 143821857:143821857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.168G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000526683 |
| Start | 143818216:143818217(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.578_579dupTG |
| AA Mutation | p.Met194Ter(p.M194*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |