Primary Site >> Stomach Cancer
Gene >> MYO6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75914102:75914102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3479G>A |
| AA Mutation | p.Arg1160Gln(p.R1160Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75914152:75914152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146419641 |
| CDS Mutation | c.3529C>T |
| AA Mutation | p.Arg1177Cys(p.R1177C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75914969:75914969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3815G>A |
| AA Mutation | p.Arg1272Gln(p.R1272Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75881794:75881794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2392T>C |
| AA Mutation | p.Trp798Arg(p.W798R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75907690:75907690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3262A>G |
| AA Mutation | p.Thr1088Ala(p.T1088A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75855262:75855262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747375619 |
| CDS Mutation | c.1202G>A |
| AA Mutation | p.Gly401Asp(p.G401D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75914129:75914129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763284731 |
| CDS Mutation | c.3506G>A |
| AA Mutation | p.Arg1169His(p.R1169H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75830497:75830497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.343T>C |
| AA Mutation | p.Tyr115His(p.Y115H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75914872:75914872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745915772 |
| CDS Mutation | c.3718C>T |
| AA Mutation | p.Arg1240Cys(p.R1240C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75822843:75822843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.179A>G |
| AA Mutation | p.Glu60Gly(p.E60G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75908601:75908601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779885818 |
| CDS Mutation | c.3386G>A |
| AA Mutation | p.Arg1129His(p.R1129H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75862649:75862649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757665143 |
| CDS Mutation | c.1600C>T |
| AA Mutation | p.Arg534Cys(p.R534C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75873223:75873223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2000G>T |
| AA Mutation | p.Arg667Leu(p.R667L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369977 |
| Start | 75890235:75890235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781754117 |
| CDS Mutation | c.2837G>A |
| AA Mutation | p.Arg946His(p.R946H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369977 |
| Start | 75914067:75914067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3444G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369977 |
| Start | 75841372:75841372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.810T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369977 |
| Start | 75892682:75892682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374917329 |
| CDS Mutation | c.3099G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369977 |
| Start | 75822830:75822830(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.171delA |
| AA Mutation | p.Asp58MetfsTer8(p.D58Mfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369977 |
| Start | 75898401:75898401(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3170delT |
| AA Mutation | p.Leu1057Ter(p.L1057*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000369977 |
| Start | 75895230:75895230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3108-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000369977 |
| Start | 75895261:75895261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200713129 |
| CDS Mutation | c.3137+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |