Primary Site >> Pancreatic Cancer
Gene >> FAT2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151565700:151565700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142737825 |
| CDS Mutation | c.3232G>A |
| AA Mutation | p.Ala1078Thr(p.A1078T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151528126:151528126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10034C>T |
| AA Mutation | p.Ala3345Val(p.A3345V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151531707:151531707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9691G>A |
| AA Mutation | p.Ala3231Thr(p.A3231T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151507459:151507459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12212G>A |
| AA Mutation | p.Arg4071His(p.R4071H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151540599:151540599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9007G>A |
| AA Mutation | p.Asp3003Asn(p.D3003N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151545703:151545703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5424G>T |
| AA Mutation | p.Glu1808Asp(p.E1808D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151550634:151550634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4534T>G |
| AA Mutation | p.Leu1512Val(p.L1512V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151554442:151554442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3865G>A |
| AA Mutation | p.Glu1289Lys(p.E1289K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151567700:151567700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748234388 |
| CDS Mutation | c.1232G>A |
| AA Mutation | p.Arg411Gln(p.R411Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151568331:151568331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372731700 |
| CDS Mutation | c.601G>A |
| AA Mutation | p.Gly201Ser(p.G201S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151568784:151568784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.148A>G |
| AA Mutation | p.Thr50Ala(p.T50A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151544381:151544381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6746C>A |
| AA Mutation | p.Ala2249Asp(p.A2249D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151512251:151512251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11819C>T |
| AA Mutation | p.Ala3940Val(p.A3940V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151506027:151506027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12588C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151546200:151546200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4927C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151550794:151550794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4374C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151566072:151566072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752153320 |
| CDS Mutation | c.2860C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000261800 |
| Start | 151531971:151531971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9428-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |