Primary Site >> Esophagus Cancer
Gene >> MUC5B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1232052:1232052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1735G>T |
| AA Mutation | p.Val579Leu(p.V579L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1230957:1230957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368620070 |
| CDS Mutation | c.1492G>A |
| AA Mutation | p.Gly498Ser(p.G498S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1261396:1261396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.17077G>A |
| AA Mutation | p.Ala5693Thr(p.A5693T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1242801:1242801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5921C>A |
| AA Mutation | p.Thr1974Lys(p.T1974K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1239536:1239536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3553C>A |
| AA Mutation | p.His1185Asn(p.H1185N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1242276:1242276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5396C>A |
| AA Mutation | p.Pro1799Gln(p.P1799Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1251396:1251396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375836524 |
| CDS Mutation | c.14516C>A |
| AA Mutation | p.Ser4839Tyr(p.S4839Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1250439:1250439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13559C>A |
| AA Mutation | p.Thr4520Asn(p.T4520N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1226627:1226627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369252177 |
| CDS Mutation | c.212C>T |
| AA Mutation | p.Ala71Val(p.A71V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244732:1244732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7852G>T |
| AA Mutation | p.Ala2618Ser(p.A2618S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1249403:1249403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12523C>T |
| AA Mutation | p.Arg4175Cys(p.R4175C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1242024:1242024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5144C>A |
| AA Mutation | p.Pro1715His(p.P1715H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1252902:1252902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372794013 |
| CDS Mutation | c.15139G>A |
| AA Mutation | p.Val5047Ile(p.V5047I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1241790:1241790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776605835 |
| CDS Mutation | c.4910C>T |
| AA Mutation | p.Pro1637Leu(p.P1637L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1251029:1251029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201216315 |
| CDS Mutation | c.14149G>A |
| AA Mutation | p.Ala4717Thr(p.A4717T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1257245:1257245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.16243G>A |
| AA Mutation | p.Val5415Met(p.V5415M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1226229:1226229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754603108 |
| CDS Mutation | c.152G>A |
| AA Mutation | p.Arg51Gln(p.R51Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1252374:1252374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14895C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1235205:1235205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745400423 |
| CDS Mutation | c.2751C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1258962:1258962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.16614C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1252904:1252904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15141C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1248751:1248751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11871C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1248607:1248607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11727C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000529681 |
| Start | 1226277:1226277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780122976 |
| CDS Mutation | c.199+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |