Primary Site >> Pancreatic Cancer
Gene >> CSMD2
| ID | 1 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000241312 |
| Start | 33626519:33626519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529128430 |
| CDS Mutation | c.5143G>A |
| AA Mutation | p.Ala1715Thr(p.A1715T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000241312 |
| Start | 33546133:33546133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8572C>T |
| AA Mutation | p.Arg2858Cys(p.R2858C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000241312 |
| Start | 33819824:33819824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369228743 |
| CDS Mutation | c.1093G>A |
| AA Mutation | p.Val365Ile(p.V365I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000241312 |
| Start | 33935880:33935880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767673294 |
| CDS Mutation | c.472G>A |
| AA Mutation | p.Gly158Ser(p.G158S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000241312 |
| Start | 33533885:33533885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753503294 |
| CDS Mutation | c.9470G>A |
| AA Mutation | p.Arg3157His(p.R3157H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000241312 |
| Start | 33692955:33692955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756045595 |
| CDS Mutation | c.3907G>A |
| AA Mutation | p.Glu1303Lys(p.E1303K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000241312 |
| Start | 33918104:33918104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.790T>A |
| AA Mutation | p.Ser264Thr(p.S264T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000241312 |
| Start | 33602423:33602423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373586316 |
| CDS Mutation | c.6662G>A |
| AA Mutation | p.Arg2221His(p.R2221H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant;NMD_transcript_variant |
| Transcription ID | ENST00000241312 |
| Start | 33743413:33743413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547519483 |
| CDS Mutation | c.1920C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant;NMD_transcript_variant |
| Transcription ID | ENST00000241312 |
| Start | 33657989:33657989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4284C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |