Primary Site >> Liver Cancer
Gene >> MUC5B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1249691:1249691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12811T>A |
| AA Mutation | p.Ser4271Thr(p.S4271T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1246419:1246419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369158178 |
| CDS Mutation | c.9539C>T |
| AA Mutation | p.Thr3180Met(p.T3180M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1254299:1254299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15425C>A |
| AA Mutation | p.Ser5142Tyr(p.S5142Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1245588:1245588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs535181655 |
| CDS Mutation | c.8708C>T |
| AA Mutation | p.Ala2903Val(p.A2903V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1243260:1243260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6380G>A |
| AA Mutation | p.Ser2127Asn(p.S2127N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1248153:1248153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765539013 |
| CDS Mutation | c.11273C>T |
| AA Mutation | p.Thr3758Met(p.T3758M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1246062:1246062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9182C>A |
| AA Mutation | p.Ser3061Tyr(p.S3061Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1241693:1241693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4813G>A |
| AA Mutation | p.Gly1605Arg(p.G1605R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1229777:1229777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1190G>A |
| AA Mutation | p.Gly397Asp(p.G397D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1245533:1245533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8653T>A |
| AA Mutation | p.Tyr2885Asn(p.Y2885N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1259010:1259010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.16662C>A |
| AA Mutation | p.Asp5554Glu(p.D5554E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244855:1244855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7975C>T |
| AA Mutation | p.Pro2659Ser(p.P2659S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1256759:1256759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.16225G>A |
| AA Mutation | p.Val5409Met(p.V5409M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1243976:1243976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7096C>A |
| AA Mutation | p.Pro2366Thr(p.P2366T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1248376:1248376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11496C>A |
| AA Mutation | p.His3832Gln(p.H3832Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1241409:1241409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4529C>A |
| AA Mutation | p.Thr1510Lys(p.T1510K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1245154:1245154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8274C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244524:1244524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7644C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1239839:1239839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3624T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1227763:1227763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781163769 |
| CDS Mutation | c.756C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1247722:1247722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10842C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1235112:1235112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769335872 |
| CDS Mutation | c.2658C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1226685:1226685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377569377 |
| CDS Mutation | c.270C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1243156:1243156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6276C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1249954:1249954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13074G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1237050:1237050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3183C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1249430:1249430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774559269 |
| CDS Mutation | c.12550C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1247236:1247236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10356C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000529681 |
| Start | 1259029:1259029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.16681G>T |
| AA Mutation | p.Glu5561Ter(p.E5561*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |