Primary Site >> Pancreatic Cancer
Gene >> ATR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350721 |
| Start | 142493179:142493179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6031G>A |
| AA Mutation | p.Glu2011Lys(p.E2011K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350721 |
| Start | 142513553:142513553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4589C>A |
| AA Mutation | p.Pro1530Gln(p.P1530Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350721 |
| Start | 142524021:142524021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4124A>G |
| AA Mutation | p.Glu1375Gly(p.E1375G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350721 |
| Start | 142550205:142550205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2903G>T |
| AA Mutation | p.Arg968Ile(p.R968I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350721 |
| Start | 142562937:142562937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.465C>A |
| AA Mutation | p.Asp155Glu(p.D155E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350721 |
| Start | 142466385:142466385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6836A>C |
| AA Mutation | p.Asn2279Thr(p.N2279T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350721 |
| Start | 142562550:142562550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.852T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_retained_variant |
| Transcription ID | ENST00000350721 |
| Start | 142449430:142449430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7934G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350721 |
| Start | 142467994:142467994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6627G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350721 |
| Start | 142522776:142522776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770181975 |
| CDS Mutation | c.4218G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000350721 |
| Start | 142524125:142524162(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3983_4020delTAGAACCTATTATCTCACAGTTGGTGACAGTGCTTTTG |
| AA Mutation | p.Val1328GlufsTer35(p.V1328Efs*35) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000350721 |
| Start | 142499714:142499714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5293G>T |
| AA Mutation | p.Glu1765Ter(p.E1765*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |