Primary Site >> Stomach Cancer
Gene >> SLC22A12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377574 |
| Start | 64591867:64591867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.311C>T |
| AA Mutation | p.Thr104Met(p.T104M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377574 |
| Start | 64591890:64591890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772733867 |
| CDS Mutation | c.334G>A |
| AA Mutation | p.Asp112Asn(p.D112N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377574 |
| Start | 64591584:64591584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.28G>A |
| AA Mutation | p.Val10Met(p.V10M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377574 |
| Start | 64599870:64599870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1265C>T |
| AA Mutation | p.Ala422Val(p.A422V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377574 |
| Start | 64600759:64600759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1419G>C |
| AA Mutation | p.Gln473His(p.Q473H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377574 |
| Start | 64592867:64592867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.491G>A |
| AA Mutation | p.Gly164Asp(p.G164D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377574 |
| Start | 64599701:64599701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1096G>A |
| AA Mutation | p.Gly366Ser(p.G366S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377574 |
| Start | 64600779:64600779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1439C>T |
| AA Mutation | p.Ala480Val(p.A480V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377574 |
| Start | 64591822:64591822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201567912 |
| CDS Mutation | c.266G>A |
| AA Mutation | p.Arg89His(p.R89H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377574 |
| Start | 64591901:64591901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776503281 |
| CDS Mutation | c.345G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377574 |
| Start | 64592865:64592865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780944605 |
| CDS Mutation | c.489C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377574 |
| Start | 64600416:64600416(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1339delG |
| AA Mutation | p.Ala447LeufsTer20(p.A447Lfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |