Primary Site >> Pancreatic Cancer
Gene >> MUC5B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1229181:1229181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.988C>G |
| AA Mutation | p.Pro330Ala(p.P330A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1241187:1241187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758850391 |
| CDS Mutation | c.4307C>T |
| AA Mutation | p.Pro1436Leu(p.P1436L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1250825:1250825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373476136 |
| CDS Mutation | c.13945G>A |
| AA Mutation | p.Ala4649Thr(p.A4649T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1230538:1230538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371537386 |
| CDS Mutation | c.1408G>A |
| AA Mutation | p.Gly470Ser(p.G470S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1236958:1236958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3091G>A |
| AA Mutation | p.Asp1031Asn(p.D1031N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1240917:1240917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4037G>T |
| AA Mutation | p.Gly1346Val(p.G1346V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244480:1244480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7600G>T |
| AA Mutation | p.Ala2534Ser(p.A2534S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244945:1244945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8065T>C |
| AA Mutation | p.Ser2689Pro(p.S2689P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1246914:1246914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10034C>T |
| AA Mutation | p.Ser3345Phe(p.S3345F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1251162:1251162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs190661408 |
| CDS Mutation | c.14282C>T |
| AA Mutation | p.Thr4761Met(p.T4761M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1258354:1258354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.16580G>T |
| AA Mutation | p.Gly5527Val(p.G5527V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1243756:1243756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746190435 |
| CDS Mutation | c.6876C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1245916:1245916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs563936822 |
| CDS Mutation | c.9036G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1249591:1249591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12711G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1254738:1254738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756191731 |
| CDS Mutation | c.15522C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000529681 |
| Start | 1242370:1242370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5490C>A |
| AA Mutation | p.Cys1830Ter(p.C1830*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000529681 |
| Start | 1231422:1231422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1541-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |