Primary Site >> Stomach Cancer
Gene >> NXN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336868 |
| Start | 822370:822370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370296358 |
| CDS Mutation | c.700G>A |
| AA Mutation | p.Val234Ile(p.V234I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336868 |
| Start | 826020:826020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.419C>T |
| AA Mutation | p.Ala140Val(p.A140V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336868 |
| Start | 803777:803777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1030G>A |
| AA Mutation | p.Ala344Thr(p.A344T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336868 |
| Start | 805173:805173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.895G>A |
| AA Mutation | p.Asp299Asn(p.D299N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336868 |
| Start | 801118:801118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1139A>T |
| AA Mutation | p.Asp380Val(p.D380V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336868 |
| Start | 826033:826033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.406A>C |
| AA Mutation | p.Ile136Leu(p.I136L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336868 |
| Start | 825979:825979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.460A>T |
| AA Mutation | p.Ile154Phe(p.I154F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336868 |
| Start | 819456:819456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777902672 |
| CDS Mutation | c.803G>A |
| AA Mutation | p.Arg268Gln(p.R268Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336868 |
| Start | 822453:822453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139124108 |
| CDS Mutation | c.617C>T |
| AA Mutation | p.Pro206Leu(p.P206L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336868 |
| Start | 819465:819465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757420440 |
| CDS Mutation | c.794G>A |
| AA Mutation | p.Arg265His(p.R265H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336868 |
| Start | 825995:825995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.444G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336868 |
| Start | 805213:805213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770149423 |
| CDS Mutation | c.855C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336868 |
| Start | 801015:801015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1242C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336868 |
| Start | 805108:805108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752204586 |
| CDS Mutation | c.960C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |