Primary Site >> Liver Cancer
Gene >> FAT2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151567049:151567049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1883T>C |
| AA Mutation | p.Leu628Pro(p.L628P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151545647:151545647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5480A>G |
| AA Mutation | p.Glu1827Gly(p.E1827G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151566293:151566293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2639A>C |
| AA Mutation | p.His880Pro(p.H880P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151566563:151566563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2369T>C |
| AA Mutation | p.Val790Ala(p.V790A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151545595:151545595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5532C>A |
| AA Mutation | p.Asp1844Glu(p.D1844E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151507307:151507307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12364G>T |
| AA Mutation | p.Ala4122Ser(p.A4122S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151565914:151565914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764080414 |
| CDS Mutation | c.3018G>T |
| AA Mutation | p.Arg1006Ser(p.R1006S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151525890:151525890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10384T>A |
| AA Mutation | p.Tyr3462Asn(p.Y3462N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151566704:151566704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2228A>T |
| AA Mutation | p.Asp743Val(p.D743V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151567102:151567102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1830T>A |
| AA Mutation | p.Phe610Leu(p.F610L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151566287:151566287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2645A>G |
| AA Mutation | p.Asp882Gly(p.D882G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151507597:151507597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538316910 |
| CDS Mutation | c.12074C>T |
| AA Mutation | p.Ala4025Val(p.A4025V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151550628:151550628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556459301 |
| CDS Mutation | c.4540C>T |
| AA Mutation | p.Leu1514Phe(p.L1514F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000261800 |
| Start | 151554364:151554364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3943A>T |
| AA Mutation | p.Thr1315Ser(p.T1315S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151531719:151531719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9679G>T |
| AA Mutation | p.Val3227Leu(p.V3227L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151529315:151529315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9889A>G |
| AA Mutation | p.Ser3297Gly(p.S3297G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151542427:151542427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8700T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151565758:151565758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542235186 |
| CDS Mutation | c.3174C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151568713:151568713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.219C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151545625:151545625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5502C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151543216:151543216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7911C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151505940:151505940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12675C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151543494:151543494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759347576 |
| CDS Mutation | c.7633C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151567837:151567837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1095T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151507224:151507224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758682292 |
| CDS Mutation | c.12447G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |