Primary Site >> Stomach Cancer
Gene >> SLC44A4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229729 |
| Start | 31870887:31870887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763411450 |
| CDS Mutation | c.862G>A |
| AA Mutation | p.Ala288Thr(p.A288T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229729 |
| Start | 31865906:31865906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1454T>C |
| AA Mutation | p.Phe485Ser(p.F485S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000229729 |
| Start | 31865874:31865874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781022323 |
| CDS Mutation | c.1486C>T |
| AA Mutation | p.Arg496Cys(p.R496C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229729 |
| Start | 31865776:31865776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1496C>A |
| AA Mutation | p.Thr499Asn(p.T499N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229729 |
| Start | 31866107:31866107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568729174 |
| CDS Mutation | c.1253C>T |
| AA Mutation | p.Ser418Leu(p.S418L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229729 |
| Start | 31865903:31865903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779511700 |
| CDS Mutation | c.1457C>T |
| AA Mutation | p.Pro486Leu(p.P486L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229729 |
| Start | 31863712:31863712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2048G>T |
| AA Mutation | p.Arg683Leu(p.R683L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229729 |
| Start | 31870836:31870836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774489026 |
| CDS Mutation | c.913G>A |
| AA Mutation | p.Val305Met(p.V305M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229729 |
| Start | 31871355:31871355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.660G>T |
| AA Mutation | p.Lys220Asn(p.K220N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229729 |
| Start | 31865744:31865744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1528A>G |
| AA Mutation | p.Thr510Ala(p.T510A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229729 |
| Start | 31865345:31865345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748439826 |
| CDS Mutation | c.1730C>T |
| AA Mutation | p.Ala577Val(p.A577V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229729 |
| Start | 31865989:31865989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1371A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000229729 |
| Start | 31878973:31878973(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs760348287 |
| CDS Mutation | c.8delG |
| AA Mutation | p.Gly3GlufsTer44(p.G3Efs*44) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000229729 |
| Start | 31865348:31865348(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1727delA |
| AA Mutation | p.Asn576MetfsTer67(p.N576Mfs*67) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000229729 |
| Start | 31878972:31878973(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.8dupG |
| AA Mutation | p.Gln5AlafsTer6(p.Q5Afs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |