Primary Site >> Stomach Cancer
Gene >> MLXIPL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313375 |
| Start | 73596918:73596918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1618G>A |
| AA Mutation | p.Ala540Thr(p.A540T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313375 |
| Start | 73599572:73599572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782609622 |
| CDS Mutation | c.1025C>T |
| AA Mutation | p.Pro342Leu(p.P342L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313375 |
| Start | 73594286:73594286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376618696 |
| CDS Mutation | c.2428G>A |
| AA Mutation | p.Ala810Thr(p.A810T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313375 |
| Start | 73597224:73597224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1561G>A |
| AA Mutation | p.Ala521Thr(p.A521T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313375 |
| Start | 73593975:73593975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2449A>G |
| AA Mutation | p.Asn817Asp(p.N817D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313375 |
| Start | 73596387:73596387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367912576 |
| CDS Mutation | c.1915C>T |
| AA Mutation | p.Arg639Trp(p.R639W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313375 |
| Start | 73595909:73595909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782546883 |
| CDS Mutation | c.2119C>T |
| AA Mutation | p.Arg707Cys(p.R707C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000313375 |
| Start | 73596639:73596639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782157345 |
| CDS Mutation | c.1822G>A |
| AA Mutation | p.Gly608Ser(p.G608S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313375 |
| Start | 73593977:73593977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2447T>G |
| AA Mutation | p.Leu816Arg(p.L816R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313375 |
| Start | 73596395:73596395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1907T>C |
| AA Mutation | p.Ile636Thr(p.I636T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313375 |
| Start | 73595666:73595666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2281C>T |
| AA Mutation | p.Arg761Cys(p.R761C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313375 |
| Start | 73596226:73596226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781786522 |
| CDS Mutation | c.1985G>A |
| AA Mutation | p.Arg662His(p.R662H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313375 |
| Start | 73597678:73597678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370237317 |
| CDS Mutation | c.1107C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |