Primary Site >> Pancreatic Cancer
Gene >> DST
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312431 |
| Start | 56460250:56460250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532258725 |
| CDS Mutation | c.16232C>T |
| AA Mutation | p.Thr5411Met(p.T5411M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312431 |
| Start | 56463608:56463608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201429821 |
| CDS Mutation | c.16073C>T |
| AA Mutation | p.Ala5358Val(p.A5358V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312431 |
| Start | 56477401:56477401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14848G>A |
| AA Mutation | p.Asp4950Asn(p.D4950N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000312431 |
| Start | 56529450:56529450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766911461 |
| CDS Mutation | c.10822C>T |
| AA Mutation | p.Arg3608Trp(p.R3608W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312431 |
| Start | 56629325:56629325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3887A>C |
| AA Mutation | p.Asp1296Ala(p.D1296A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312431 |
| Start | 56634157:56634157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3083G>A |
| AA Mutation | p.Arg1028Lys(p.R1028K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312431 |
| Start | 56639553:56639553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778615450 |
| CDS Mutation | c.2243C>T |
| AA Mutation | p.Ala748Val(p.A748V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312431 |
| Start | 56640537:56640537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767792412 |
| CDS Mutation | c.1583G>A |
| AA Mutation | p.Arg528His(p.R528H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312431 |
| Start | 56651231:56651231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.715G>T |
| AA Mutation | p.Asp239Tyr(p.D239Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312431 |
| Start | 56670765:56670765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.577G>A |
| AA Mutation | p.Ala193Thr(p.A193T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312431 |
| Start | 56552859:56552859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774732469 |
| CDS Mutation | c.9162C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312431 |
| Start | 56627284:56627284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4129C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312431 |
| Start | 56635607:56635607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2655C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312431 |
| Start | 56851524:56851524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.84T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312431 |
| Start | 56493018:56493018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13695T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000312431 |
| Start | 56528895:56528895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10855C>T |
| AA Mutation | p.Gln3619Ter(p.Q3619*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000312431 |
| Start | 56628089:56628089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4035G>A |
| AA Mutation | p.Trp1345Ter(p.W1345*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |