Primary Site >> Stomach Cancer
Gene >> SYNM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336292 |
| Start | 99129986:99129986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1626G>T |
| AA Mutation | p.Leu542Phe(p.L542F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336292 |
| Start | 99132820:99132820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530141940 |
| CDS Mutation | c.4460G>A |
| AA Mutation | p.Arg1487His(p.R1487H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336292 |
| Start | 99132400:99132400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4040G>A |
| AA Mutation | p.Gly1347Asp(p.G1347D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336292 |
| Start | 99130294:99130294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1934G>A |
| AA Mutation | p.Ser645Asn(p.S645N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336292 |
| Start | 99130839:99130839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369788122 |
| CDS Mutation | c.2479G>A |
| AA Mutation | p.Glu827Lys(p.E827K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336292 |
| Start | 99130696:99130696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2336G>A |
| AA Mutation | p.Gly779Asp(p.G779D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336292 |
| Start | 99129817:99129817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1457G>C |
| AA Mutation | p.Ser486Thr(p.S486T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336292 |
| Start | 99129979:99129979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1619A>G |
| AA Mutation | p.Glu540Gly(p.E540G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336292 |
| Start | 99131115:99131115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376246829 |
| CDS Mutation | c.2755G>A |
| AA Mutation | p.Glu919Lys(p.E919K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336292 |
| Start | 99113688:99113688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.908G>A |
| AA Mutation | p.Gly303Asp(p.G303D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336292 |
| Start | 99130271:99130271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367995539 |
| CDS Mutation | c.1911C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336292 |
| Start | 99131045:99131045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376459305 |
| CDS Mutation | c.2685G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |