Primary Site >> Stomach Cancer
Gene >> MTR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236886313:236886313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2797A>C |
| AA Mutation | p.Ser933Arg(p.S933R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236838441:236838441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1357T>G |
| AA Mutation | p.Phe453Val(p.F453V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236861237:236861237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2156T>C |
| AA Mutation | p.Val719Ala(p.V719A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236853059:236853059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1924G>A |
| AA Mutation | p.Ala642Thr(p.A642T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236894486:236894486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3334A>C |
| AA Mutation | p.Lys1112Gln(p.K1112Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236863499:236863499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2350G>A |
| AA Mutation | p.Val784Met(p.V784M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236894411:236894411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3259G>A |
| AA Mutation | p.Ala1087Thr(p.A1087T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236829248:236829248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1055A>C |
| AA Mutation | p.Glu352Ala(p.E352A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236824192:236824192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.838G>A |
| AA Mutation | p.Ala280Thr(p.A280T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236874737:236874737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2485C>A |
| AA Mutation | p.Leu829Met(p.L829M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236838490:236838490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1406T>C |
| AA Mutation | p.Val469Ala(p.V469A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236894435:236894435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3283G>A |
| AA Mutation | p.Asp1095Asn(p.D1095N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236891261:236891261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3136C>A |
| AA Mutation | p.Leu1046Met(p.L1046M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236880781:236880781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764999575 |
| CDS Mutation | c.2621C>T |
| AA Mutation | p.Pro874Leu(p.P874L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236803535:236803535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769395060 |
| CDS Mutation | c.142G>A |
| AA Mutation | p.Glu48Lys(p.E48K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236891267:236891267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756706737 |
| CDS Mutation | c.3142G>A |
| AA Mutation | p.Ala1048Thr(p.A1048T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236897113:236897113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3706G>C |
| AA Mutation | p.Asp1236His(p.D1236H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236831992:236831992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1102T>C |
| AA Mutation | p.Tyr368His(p.Y368H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366577 |
| Start | 236891273:236891273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3148G>A |
| AA Mutation | p.Ala1050Thr(p.A1050T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366577 |
| Start | 236863504:236863504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761121279 |
| CDS Mutation | c.2355C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366577 |
| Start | 236803534:236803534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144151735 |
| CDS Mutation | c.141C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366577 |
| Start | 236886333:236886333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2817T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366577 |
| Start | 236863474:236863474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2325C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366577 |
| Start | 236859878:236859878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1999A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366577 |
| Start | 236897103:236897103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3696G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366577 |
| Start | 236824185:236824185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.831T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366577 |
| Start | 236852532:236852532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760490684 |
| CDS Mutation | c.1707T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000366577 |
| Start | 236863553:236863553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138695265 |
| CDS Mutation | c.2404C>T |
| AA Mutation | p.Arg802Ter(p.R802*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |