Primary Site >> Stomach Cancer
Gene >> NUP62
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352066 |
| Start | 49908970:49908970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.838A>G |
| AA Mutation | p.Thr280Ala(p.T280A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352066 |
| Start | 49908763:49908763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758695990 |
| CDS Mutation | c.1045C>T |
| AA Mutation | p.Arg349Trp(p.R349W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352066 |
| Start | 49908619:49908619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1189C>A |
| AA Mutation | p.Leu397Met(p.L397M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352066 |
| Start | 49908963:49908963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149572563 |
| CDS Mutation | c.845C>G |
| AA Mutation | p.Thr282Ser(p.T282S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352066 |
| Start | 49908823:49908823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.985A>G |
| AA Mutation | p.Thr329Ala(p.T329A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352066 |
| Start | 49908279:49908279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142980354 |
| CDS Mutation | c.1529G>A |
| AA Mutation | p.Arg510His(p.R510H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352066 |
| Start | 49908971:49908971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.837C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352066 |
| Start | 49908428:49908428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780484739 |
| CDS Mutation | c.1380G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352066 |
| Start | 49909256:49909256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.552A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352066 |
| Start | 49908716:49908716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762609312 |
| CDS Mutation | c.1092G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000352066 |
| Start | 49908548:49908549(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1259_1260delCC |
| AA Mutation | p.Thr420AsnfsTer8(p.T420Nfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |