Primary Site >> Stomach Cancer
Gene >> HNRNPL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221419 |
| Start | 38837440:38837440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1655A>G |
| AA Mutation | p.Lys552Arg(p.K552R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221419 |
| Start | 38838464:38838464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1490A>G |
| AA Mutation | p.Gln497Arg(p.Q497R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221419 |
| Start | 38840532:38840532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.908G>A |
| AA Mutation | p.Arg303His(p.R303H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221419 |
| Start | 38843910:38843910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.812C>T |
| AA Mutation | p.Thr271Ile(p.T271I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221419 |
| Start | 38845872:38845872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.605C>T |
| AA Mutation | p.Pro202Leu(p.P202L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221419 |
| Start | 38838513:38838513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1441C>T |
| AA Mutation | p.Arg481Trp(p.R481W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221419 |
| Start | 38844080:38844080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.735G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221419 |
| Start | 38838504:38838504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1450C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221419 |
| Start | 38846021:38846021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.456C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221419 |
| Start | 38840327:38840327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751667827 |
| CDS Mutation | c.1002G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000221419 |
| Start | 38838988:38838988(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1261delG |
| AA Mutation | p.Ala421ProfsTer12(p.A421Pfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000221419 |
| Start | 38837401:38837402(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1690_1693dupCATT |
| AA Mutation | p.Tyr565SerfsTer69(p.Y565Sfs*69) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | splice_acceptor_variant;coding_sequence_variant |
| Transcription ID | ENST00000221419 |
| Start | 38838591:38838599(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1356-1_1363delGTGTCTCCA |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |