SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs137940558 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013715 | AAGTAATGATGCTTC[C/T]TGGAATCAGTGGTGT | 26259 |
rs137981385 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934723 | CCATTGGTAATATCC[C/T]GCATAACTACAGAAC | 26259 |
rs137996443 | in-del | -/T | 0.112631 | 0.208878 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999625 | CTCCTCACGGTCCAC[-/T]TCAGGTTTTCTCAGA | 26259 |
rs138014698 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116997668 | GAAGGGGGTTCCATC[A/G]GCTGGAAGCAGCACC | 26259 |
rs138020987 | snp | A/G | 6.59055e-05 | 0.00574007 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024244 | GATGACTGGAAGATC[A/G]TCAGTGGAGGCGAGG | 26259 |
rs138068562 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966008 | GCTCAAACTATCCAC[C/T]TGCTTCAGCCTCCCA | 26259 |
rs138077991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027383 | ACGAGCTCTCTCCCA[C/T]TGCCTTCCAGGCACC | 26259 |
rs138083262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007651 | TACACCTCTGAGAAT[A/G]AGTCAAGTGGTCATG | 26259 |
rs138087117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929192 | TTATGCCATTAACAT[C/T]GTTCTCTTGTTCTCG | 26259 |
rs138129688 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921765 | GAAGAAAATAAAAGT[C/G/T]TTTAGTAATATAATT | 26259 |
rs138169354 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945683 | GACTTGTTGCCCATT[C/T]TGTTCACCATTAGAT | 26259 |
rs138171433 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910175 | TGAGATTTTGGTGCA[A/C]GCATCACCCGAGCAG | 26259 |
rs138177380 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023036 | TATCCACAGGTAGTT[C/G]ACTTTGAGTCCTTTT | 26259 |
rs138191485 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991038 | GTGTTTTCGCTGGTG[G/T]TTTAAAATTAGGAGT | 26259 |
rs138197096 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961937 | CGGGTGTGAATGTGA[A/G]GTGTTGGGGGATTTG | 26259 |
rs138235760 | in-del | -/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937215 | GCATGTGTGGGTATG[-/G]GGGGAAGATCACTCA | 26259 |
rs138288044 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018668 | CTTTTTCCCAGGGGG[G/T]AGAAATTCAAGGCTG | 26259 |
rs138310702 | in-del | -/TA | 0.117188 | 0.211804 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975282 | ATAAACTGGGTGACT[-/TA]TAAACAACAGAAGTA | 26259 |
rs138310939 | snp | A/G | 0.000610758 | 0.0174644 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027439 | CCACAGCCTCATCAC[A/G]GCCAACGTGCCTTAC | 26259 |
rs138329489 | snp | A/G | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030306 | GCAGGCAGATGGACC[A/G]GAGGGTTTTCTGCTT | 26259 |
rs138390667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924340 | ATATTTATGGGGCAC[A/G]GTGTCATATATGTAT | 26259 |
rs138454816 | snp | C/T | 0.00781559 | 0.0620219 | synonymous-codon, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985264 | TCATCGTTTTGAGCA[C/T]GATGCAAGAATACAG | 26259 |
rs138499062 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940030 | CTGAGTCGTTATCCC[A/G]TTCTTTATTGCCTGA | 26259 |
rs138505453 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929494 | CCCACCTCAGCCTCC[C/T]AAAGTGCTGGGATTA | 26259 |
rs138509753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007858 | GAAATGGTAAAGGTC[A/G]TTAAGGGACTCGTAA | 26259 |
rs138535442 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934137 | ACAAACCATGCCGGA[C/G]ACTGATTTTGCTTTG | 26259 |
rs138540315 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013397 | AAAGTGAGATTTTGC[A/T]TAGGAGTTTTATCAG | 26259 |
rs138548106 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981040 | GTACAAAACAGGGAG[C/T]TCTGTAACTACCTGT | 26259 |
rs138558875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925302 | GGCATTGCCTAGGAA[A/G]GGACTCAGCTGTGAG | 26259 |
rs138569917 | snp | C/T | 0.0174175 | 0.0916809 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030600 | AGCAATTAAAGATAA[C/T]GGAGTGTAAAGTCAT | 26259 |
rs138590080 | in-del | -/TATGCTGTT | 0.00795532 | 0.062565 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014705 | AAGCTGTTCAATTTC[-/TATGCTGTT]TTTGGTCTGCGCATG | 26259 |
rs138622771 | snp | A/C | 0.000544029 | 0.0164839 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945506 | GCCGAGCCAAGGAAC[A/C]CATGTTACGAACCAA | 26259 |
rs138683433 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921586 | GTAGACCATTTCTTA[C/T]ATACTTGCTAACAGC | 26259 |
rs138687480 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027073 | CAGCGATGGGCCAGT[C/G]TCTGTTGCATGTGGC | 26259 |
rs138691585 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999204 | CGGTCGCATCCCAAA[C/G]TAAGGGACTCAGGAA | 26259 |
rs138718240 | snp | A/G | 8.26945e-05 | 0.00642965 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985235 | TGGGATTTAAGGACC[A/G]GAAAGTACCCTGTTC | 26259 |
rs138719666 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942716 | AACTTGTTGTTGAGC[A/G]CCTTTAGGGAATTTT | 26259 |
rs138735735 | snp | A/T | 0.0517044 | 0.152246 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986596 | TCGCCACTGCAGTCC[A/T]GCCTGGGCAACAGAG | 26259 |
rs138797197 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950887 | TTTGGTGTGAACTCC[A/G]GAAGGTACTTAGATC | 26259 |
rs138799495 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002888 | TGTTCACCTAGCTTT[A/G]TGCATGAACGTTGAT | 26259 |
rs138802315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957472 | CTGTTCGGGAACTGA[A/T]GCCCTCAAGGATCGT | 26259 |
rs138828354 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029983 | GTACAGTGGTCTATG[A/T]GGAAGAGAAAAGGTA | 26259 |
rs138831341 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955306 | GAGAGATAAGTGGAC[A/G]TGCCTTCAACTGCGA | 26259 |
rs138845279 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973191 | GATCAATAAATAAAA[-/A]GGGAGGAGAGAAAAG | 26259 |
rs138865565 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961437 | AGGCAAGAGCATTTG[A/G]GATCCTCTCTGGAAG | 26259 |
rs138910504 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980174 | TTCATTCTTCTTTTC[C/T]GAAACCAGCTTTCTC | 26259 |
rs138987101 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009207 | TGAGACCGCTTCTCT[A/C]CTTAAAAAATTTTTT | 26259 |
rs139000065 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000771 | GTACCTATCTTACAG[C/G/T]ACTGTGGAGGTCAGG | 26259 |
rs139060226 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988969 | ATATTTTTCCAGATA[C/T]ATCAGGCCAGTATAT | 26259 |
rs139120742 | snp | A/G/T | 3.29697e-05 | 0.00406005 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028116 | CGTTCATCCTGTGAC[A/G/T]CCATGGCCACTCACT | 26259 |
rs139141667 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965070 | AGCACCCATTAAAAC[G/T]GGTGTTTAATTCCTA | 26259 |
rs139161745 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951836 | GAAAATAGTCACTCG[C/T]TGATAAACGCATTTG | 26259 |
rs139218115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022614 | GAGCCATGATGGTGC[C/T]ACTACACTCCAGCCT | 26259 |
rs139239144 | in-del | -/AT | 0.0322114 | 0.122752 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021492 | CTTCCTCCTTTGAAT[-/AT]GTTTTATAGTTTATG | 26259 |
rs139247725 | in-del | -/TTG | 0.461037 | 0.134028 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003484 | ACCCCCAAATCAACA[-/TTG]TTGTTTTTGCAGACA | 26259 |
rs139290008 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024939 | AAATACTATCCTAAG[C/T]ACAGGCTGATGGCGT | 26259 |
rs139309739 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016383 | GTGGTGATTAACATC[C/T]TTTCACGTGCTTATT | 26259 |
rs139313031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937588 | GACTGAGAAATGACC[A/G]TTGGGTTTTGCAAGT | 26259 |
rs139337099 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940250 | TTTAGCACCATCCTG[A/G]TTATCTTTTTTTTTT | 26259 |
rs139339751 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967742 | TGCCATATGTGTTTC[C/T]GATATTTTTTCCGTA | 26259 |
rs139355960 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982957 | GCCCAACTTCATGAC[A/G]TACCAAGTCATGACA | 26259 |
rs139362953 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019687 | CAGTTTCAAGAGTAA[A/C]CGAGAATGCCCGCGC | 26259 |
rs139411310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009779 | CAAGCAGAGAGTGAA[A/G]AGAAAAGTGTTTGGG | 26259 |
rs139421341 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953227 | TTTTCTCAGTTTAGA[A/C]TCATACATTTTTAAA | 26259 |
rs139429411 | snp | A/G | 0.000148634 | 0.00861944 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028047 | CGGGGGCTGATCCGC[A/G]CCTATGAGTTTGCGG | 26259 |
rs139432460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020306 | GGCTGCTTTTAGGAC[C/T]TCTTGGTCTTTGTGT | 26259 |
rs139444227 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962471 | CTCCACCCTCGCCTC[C/T]CCACTGTGTCCCCTG | 26259 |
rs139467166 | in-del | -/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987109 | ATGGCAGTGGCAGTG[-/T]TTCCCAGGTCTGCGA | 26259 |
rs139477242 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919613 | GCCTCTTGTGAATCC[C/T]TGGAGGGCAGGATCT | 26259 |
rs139485113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025462 | ATCAAGGTAAACCGA[C/T]CTCTGAGAACACAAC | 26259 |
rs139486296 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947175 | CACTTTACAAGTTAT[A/G]TACAATCTAGCTGAA | 26259 |
rs139495224 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031115 | CTGCTTTATGATGTC[C/T]GTAGTTGTTCTAATA | 26259 |
rs139590540 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020106 | GCACGGCTGCCAGTC[A/G]GCCTGTGTAGTTCTG | 26259 |
rs139617964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919054 | CAAAATAGAACAATT[A/G]CAACAGTATACTATA | 26259 |
rs139700589 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029944 | AAAAAGACAAAATAT[-/A]ACAACTCTTGATAAA | 26259 |
rs139722161 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923350 | ATAGTGGTAGAGAAT[C/T]GATATCTGAGACATT | 26259 |
rs139760206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912848 | TACTCAAATAGCATT[A/C]ATAGCTACTATTTGA | 26259 |
rs139835529 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116974100 | GGACCTAAACAGAGT[C/T]TGGTGGCCTCCCTGA | 26259 |
rs139853583 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927094 | GCTGTTGGGACACAG[A/C]GTGAAGCTTTTCCTA | 26259 |
rs139862308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926416 | CACGATTGCAAATGA[A/G]AGTTTCTTCGTGAGT | 26259 |
rs139866372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004012 | GGAAATGTATCGCGA[C/T]GCTCTGCGTGGAGCT | 26259 |
rs139880165 | snp | A/G | 0.000595642 | 0.0172472 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028033 | CTCTTTCTAGACACC[A/G]GGGGCTGATCCGCGC | 26259 |
rs139901783 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987913 | GTACTTTCTCCACCC[C/T]CACCTTGTACACATG | 26259 |
rs139903018 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927236 | TTGTGCTACCAGGAT[C/G]GTCAATGACAGCCTT | 26259 |
rs139919293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977305 | AATGGGATTTCTAAA[G/T]GCTGCAAAATGTCAT | 26259 |
rs139927035 | snp | C/T | 0.000115345 | 0.00759337 | synonymous-codon, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985303 | CCTCAGCCAGGACGA[C/T]GCAACCGTGGCCACA | 26259 |
rs139933936 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941788 | AAATAGATATTGTCT[A/G]GTATGCTATTTAAAT | 26259 |
rs139984645 | in-del | -/ACAGACCCTTTCA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026598 | CTCGTCCCCTCCTGT[-/ACAGACCCTTTCA]GCACCCCTCCCAGCC | 26259 |
rs139995963 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973382 | TCTCAAAAAATCTCC[C/T]CACTAAACACTTACT | 26259 |
rs140054295 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936084 | ATGGCAGTGAGTGCT[A/G]TGGAGAAGAACAAGA | 26259 |
rs140059571 | snp | A/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910089 | ATTTTTAAAAAAAAA[A/T]TTTTATTTCCACAGG | 26259 |
rs140073306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945822 | TCAGAGGAGTGCTCT[C/G]TGCAGCCCCTTTGAC | 26259 |
rs140074370 | in-del | -/AAAG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937991 | CAACTCTGGTGTATT[-/AAAG]AAAGACCATTAGGCC | 26259 |
rs140094596 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922810 | GAGTGTGTGTGTGTG[-/T]TGTTTTTTTTCCCTT | 26259 |
rs140117282 | in-del | -/TTTTA | 0.15698 | 0.23205 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924285 | AACACTGATAGCATC[-/TTTTA]TTTATTTATTTATTT | 26259 |
rs140120154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004725 | TATGTAGCCCTGCAG[A/G]GACCCAACTGTAGGT | 26259 |
rs140153855 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963461 | AAAAACAAACTAGCC[A/G]GACATGGTGGTGCAC | 26259 |
rs140157995 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022168 | GGATTGTTGCCCCTT[A/G]CTGGCTTCCTCAGGC | 26259 |
rs140191587 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001974 | ATTCCCAGCACCTAC[A/G]GACGTGCTGAGAGAG | 26259 |
rs140219412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979493 | AGCAGGTGGGAGTGC[C/T]AGGCCCTGCCCCTTC | 26259 |
rs140227639 | in-del | -/AT | 0.046775 | 0.145601 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008759 | ACGCACATCACTCTC[-/AT]GTGTGTGCTGAGAGG | 26259 |
rs140231738 | in-del | -/TC | 0.0821764 | 0.185298 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030464 | TCAAGCCCCGCCCTT[-/TC]TCTCTCATAGTCTTA | 26259 |
rs140232531 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013411 | CATAGGAGTTTTATC[A/G]GTGTAGATCAATGAG | 26259 |
rs140249411 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003594 | GATTTTCTGTCTCCC[-/A]AAAGTGCATTCTTTA | 26259 |
rs140268725 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913205 | ACATTATACTCTACT[G/T]TATAGCCTCCTTTGG | 26259 |
rs140275022 | snp | A/G | 8.26166e-05 | 0.00642662 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024148 | CTGGGCCTGTCCAGG[A/G]TGAGGATCCACGACC | 26259 |
rs140277877 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928976 | CTGCCATGCCCAGCT[A/G]ATTTTTGTATTTTTA | 26259 |
rs140280865 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993392 | CAGGTGTGGGCCACC[A/G]CACCCGGCCTGTTTT | 26259 |
rs140331984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978204 | GCCTTTTTCCTTTTT[C/T]GTGACCCTCCGTGGT | 26259 |
rs140373227 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017865 | AGCCAATAGGAAGCA[C/T]GCCCTGAGTTGTGAC | 26259 |
rs140394329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942141 | TGAAGCAATCCTCCT[G/T]CCTCAGTCTCACAAG | 26259 |
rs140422674 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031375 | ACCAACCGTCATCAA[C/T]AGGTTTTCTTAGAAA | 26259 |
rs140434764 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002093 | TAGGTGTTGGTTTGG[C/T]CTCACTCCGGTCCTT | 26259 |
rs140507004 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030178 | AGATTGCTTAAGATA[C/T]GCAGCCATTCCATAT | 26259 |
rs140539809 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915258 | TCTCCCAGCTCATCA[A/G]GTGTTTTTATGTGTT | 26259 |
rs140543796 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998530 | CTGGTTTACCATCCT[A/G]TACCATGGAAGAGAA | 26259 |
rs140551288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960785 | CTGCGGTAGGGCCTT[C/T]TTGAAGACTTTACAG | 26259 |
rs140575822 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954666 | ATCCTGATTGTTTTC[C/G]TAGGCTAGAGTCCTG | 26259 |
rs140597445 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002808 | GCTCCCCCTCTCCCC[-/C]AGTTGTCTATCTTTC | 26259 |
rs140644554 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920868 | TTTACTCTTTTCACA[A/G]ACCCACTGTGGTTTC | 26259 |
rs140676682 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932596 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 26259 |
rs140697469 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010667 | TTCTGAAGCACCACG[C/G]GAAGGTTTTCTTTTA | 26259 |
rs140698430 | snp | A/G | 8.23771e-05 | 0.0064173 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988784 | TCCTTTACGCCCACG[A/G]CCCGCCTGTCACATG | 26259 |
rs140717608 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915124 | GCTGATAAATGATGA[C/T]AAGGTTTATGGAAAA | 26259 |
rs140738729 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936605 | GGTAGCTTGAAGCTG[A/G]AAAAGGTAAGAAAAC | 26259 |
rs140762905 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015474 | TTAAATGAGGGCCCT[G/T]CCTATTCTGTAGCTC | 26259 |
rs140780025 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116974935 | AGGTAGGGCATCTAT[A/G]GGACAGTAGAACTAA | 26259 |
rs140785802 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018303 | TTATTTTTCCTTTCA[A/G]TGGGCAAAGTTGATG | 26259 |
rs140788681 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939540 | ATATGCTTTTGGTCC[A/C]TGTAATTAAAGAATG | 26259 |
rs140816981 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969490 | ACAGATTCAAATAAA[A/C]CCACATTTTTATATT | 26259 |
rs140845850 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978544 | TATAAATAGTCAACT[G/T]CATTCAGTATCTCTG | 26259 |
rs140890950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013025 | CAAGAAAAACCAGAC[A/G]CTTGAGGTCAGGAGT | 26259 |
rs140922176 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971042 | GTAAACTTTTTTTTT[-/T]AACACTAGGAATGCT | 26259 |
rs140973735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938587 | AACATCTTTAAGGTC[C/T]GACATATTTGAGACT | 26259 |
rs140988044 | in-del | -/CTGCCTGC | 0.0260105 | 0.111035 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001343 | GTGATCTGATTTTAG[-/CTGCCTGC]CTGCCCTCTTCTAGA | 26259 |
rs141066664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993940 | CAGTTTTATTTTTCT[A/G]CATGTGGTTATCCAA | 26259 |
rs141072341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026727 | TGGGACTGCATCTTA[C/T]CTTCTTCACTAGCTA | 26259 |
rs141082626 | snp | A/G | 3.33406e-05 | 0.00408279 | splice-acceptor-variant | FBXW8 | GRCh38.p7 | 12:116928022 | TTTTTTTTCCCCTCA[A/G]AATGAAATGAATGAT | 26259 |
rs141148558 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966581 | CATGTCTCACATCTC[A/G]TGAGCTTGAAAATAC | 26259 |
rs141187693 | in-del | -/A | 0.000964552 | 0.0219396 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964887 | TCCTCCCTATTAAGG[-/A]AAAAAAAAAGCTTTA | 26259 |
rs141198627 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996052 | GCATTAGGTTGATGA[C/G/T]GAGCCCCAGGCCTCA | 26259 |
rs141233641 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947472 | ATGAAAGGCGGCCCG[A/G]CACCGTGGGTCACTC | 26259 |
rs141254690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025986 | AGGCTTGTCCCCCAC[A/G]TGGTCACTGTTTTCA | 26259 |
rs141286666 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917890 | CCAGCTACTGGGGAG[G/T]CTGAGGCAGAAGAAT | 26259 |
rs141304705 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922548 | TCTTCACTTTTTACT[A/G]CTTTGGCTCTTAGTA | 26259 |
rs141313594 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007488 | CTATTGCCTGCAAAA[A/G]TTTGCTCTGTAATTA | 26259 |
rs141340809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960393 | GTCTCAGTTCCTGTC[A/G]ATACAGGAGACGTAG | 26259 |
rs141376912 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965677 | TAGCAGTTGGCTCAG[A/C]GGAACAAAACTAAAG | 26259 |
rs141379149 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011670 | AAGCTCCTCTCCTAG[C/G]ATCTCCACACAGGGA | 26259 |
rs141383937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998907 | TTCAAAATACACATC[A/G]CAGCTTAGACTCACA | 26259 |
rs141442528 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996178 | GCAGATTGTATTAAG[C/T]GGCACACGGCGTGCA | 26259 |
rs141448956 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954940 | CTCTCAGAGGTCACC[C/T]GTGATCTTTTGGTCA | 26259 |
rs141510012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930956 | GGGACTATAGGCTCA[C/T]GCCAACATGCCCAGC | 26259 |
rs141514982 | in-del | -/ATA | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028751 | TATAATTATATACTT[-/ATA]ATACAGTTTAGTCAT | 26259 |
rs141516778 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009214 | GCTTCTCTACTTAAA[A/C]AATTTTTTAAAAAAG | 26259 |
rs141554440 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990569 | CTCTCAGTATAGAGA[A/G]GTGATAGTTATATTC | 26259 |
rs141589189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945041 | AAAGCTCTGTATGAT[C/T]GTATAGCTAATTACC | 26259 |
rs141604043 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004189 | TGCTTATCTCATCCA[C/T]TGACTTTTTAATTTC | 26259 |
rs141606435 | in-del | -/TGTG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992787 | TGTGTGTGTGTGTGT[-/TGTG]GTGTGTGTGTATCAC | 26259 |
rs141628750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003335 | AGGTATCCAAAGGAG[C/T]TTCTGTTCCTTCCAG | 26259 |
rs141650472 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968589 | AAAACCTTGTAAAGA[C/T]GACATTTCACACAAG | 26259 |
rs141661825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929928 | TTTAAGTGAGATCAT[A/G]CAATATTTGTCTTTC | 26259 |
rs141672731 | snp | A/C/T | 0.00795532 | 0.062565 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007874 | TTAAGGGACTCGTAA[A/C/T]GTGGAAAGAACTGCC | 26259 |
rs141692420 | in-del | -/CATCCA | 0.0517044 | 0.152246 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025801 | AAACCCTGGATCAGC[-/CATCCA]CATCCAGGTCCTCAG | 26259 |
rs141766064 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962381 | CTTTGTTGTTTTGCT[A/G]TCATTTTGGCTCCGA | 26259 |
rs141777878 | snp | C/G | 0.00291614 | 0.0380732 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964778 | ATCAGAGGACGAGGA[C/G]GATGAGCCTGGAATG | 26259 |
rs141869018 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030534 | AAAAGCAGCCCCTTC[A/G]GTCTGCGTTCCCAGT | 26259 |
rs141870112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957105 | TAATCCTAGCACTTT[A/G]GGAAGTCAAGGCAGG | 26259 |
rs141902211 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910383 | CACTTAGAATAATAG[C/T]CTCCAATCCCATCCA | 26259 |
rs141905235 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019971 | AGAGGGCGAAGCGCA[C/G]CCCTCTTCCCAGCAG | 26259 |
rs141932137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955490 | CTGTGATCTGCTGGA[C/T]CTCCTGAAATGCTAG | 26259 |
rs141944972 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972773 | AATTTATGGTGTTAA[A/G]TATAGATAGAGAAGT | 26259 |
rs141989066 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909978 | AAGTGGAACGCCATC[A/G]TATGTCATTTTCTTT | 26259 |
rs141996080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945917 | AAAATGTCATTTCTA[A/G]TAAATGTAAGAGGGA | 26259 |
rs142010584 | snp | A/C/G | 0.00254081 | 0.0355525 | missense, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024319 | TGGGAGGTGTATTCC[A/C/G]GGTAAGGTGCATTCT | 26259 |
rs142018002 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028235 | TTATCCATCTTAAAA[C/T]GCCAGGCACCTCTTC | 26259 |
rs142026565 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014587 | CCAACGAATGATTTT[C/T]GTTTTGTTTTGCTTT | 26259 |
rs142041332 | in-del | -/AA | 0.0252325 | 0.109451 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947768 | AGAAAAGAAAGAAAG[-/AA]AAATGAAAGGCAGTG | 26259 |
rs142055582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951731 | GCCATGCTGCATAGG[C/T]CCAGACTGATATTTA | 26259 |
rs142075982 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909126 | GAGTCTCGCACTGTC[A/G]CCCAAGCTGGAGTGT | 26259 |
rs142085415 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989898 | CTTCTTAGAGTTGTA[A/G]GATTAAATGAAAAGC | 26259 |
rs142090073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960057 | ATAGTGGCATCTTAA[C/T]TGGTTGAGTGTAATT | 26259 |
rs142096100 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031701 | CCTGGGCGACAGAGC[A/G]AGACTTCGTCTCAAA | 26259 |
rs142122479 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913939 | CTACTAGGTTCTCTA[C/T]GAGTAGCATACAACT | 26259 |
rs142171458 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116974404 | TACATGGATTGTTGA[A/G]TGGAATCTTCAGAAG | 26259 |
rs142207231 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027900 | TGACGCTGTGTGCCC[A/G]GAGAACGCGTTTGTG | 26259 |
rs142209884 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924834 | TCTGCCTCTTGTAAG[A/G]TGTTTCTCAAATGAT | 26259 |
rs142224334 | in-del | -/GGG | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918303 | TTCAGTGGAGTGGCT[-/GGG]GTGATACCAACTTGC | 26259 |
rs142225915 | in-del | -/T | 0.0517044 | 0.152246 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021639 | CTTTGATTCTATTTA[-/T]TTTTTAAACTAGATT | 26259 |
rs142239277 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988312 | ACAAGATTATATCCC[C/G/T]ACCAGCAGTAAGTGG | 26259 |
rs142267900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968334 | TTACAAGTACAAGAA[A/G]ATATGAGTGTGTATA | 26259 |
rs142269806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936774 | ATAGGAGACTGATAC[A/G]GGGATGTGGTGAGCA | 26259 |
rs142316487 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976480 | TTTTTTTTCAAAACA[A/G]AGTCTCACTCTGTTG | 26259 |
rs142325567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926046 | GAGGATGGAGGCCAG[A/G]CCAGCTGAGTAGGCA | 26259 |
rs142367911 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982112 | AAAAGGCAACAAAAG[A/T]GGAGAAAAGGGAGCA | 26259 |
rs142398085 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929216 | GTTCTCGTCTTTTTG[A/G]CCAAGAGTGTGTGAT | 26259 |
rs142433136 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924097 | AATATTTCTAATGTC[C/T]TTAATTCCTTTTCCT | 26259 |
rs142434867 | snp | A/G | 0.000649205 | 0.018005 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928175 | CCTAAATGTGTGATT[A/G]AGGTATAGGACTCTC | 26259 |
rs142445679 | snp | C/G/T | 0.000362423 | 0.0134568 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988716 | CCCTGTGGCAGTAGC[C/G/T]GCTGCTGGAGATCTG | 26259 |
rs142471503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971191 | AACATAGTGAGCCTC[C/T]GTCTCTACAAAAAAT | 26259 |
rs142512164 | in-del | -/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941160 | TAGATCAGACTGATG[-/G]GGGGAGGTCAGCTCT | 26259 |
rs142532366 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956321 | CGCTCTTCTTACCCT[-/A]AAAAACACTCAGTTG | 26259 |
rs142537548 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920288 | TTGTGACTTACATGC[A/G]GTCTTTGTTGGAACG | 26259 |
rs142548882 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998401 | TTACAGAACCATTTA[C/G]ATTGAAGAATATCAT | 26259 |
rs142576891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943175 | TAGCTGATTTAAAGT[C/T]TCTGTTTAGTAAGTC | 26259 |
rs142622799 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012224 | TAGTGTCAAAGGGCT[C/G]TCTGGTCAGTTTGCA | 26259 |
rs142658746 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992867 | CTTTGCAGTTGTGAT[A/T]TGTCCTGCAATAAAC | 26259 |
rs142680270 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116914573 | AAAAAAAAAAAAAAA[-/A]GGCTGGGCCTGGTGG | 26259 |
rs142726510 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946622 | GAGAACCACTGTTCT[A/G]AGAGTTAGTGTGGCT | 26259 |
rs142776287 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977052 | TGGCAAAACCATCTA[-/T]TTTGTTGGGGGGATT | 26259 |
rs142795266 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961572 | AGGTGTTAAGATGTA[A/C]GACTTTATAGAGGGT | 26259 |
rs142805241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005950 | CAGCCCAGCACAGCA[C/T]CTCCTAACCTTTGGC | 26259 |
rs142808227 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950807 | TAAGTTATCGATGCT[C/T]GTTGCTAAAATGTGG | 26259 |
rs142820898 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987864 | AGGCAGCCATTGTTA[A/G]AAGATGTATGGATGT | 26259 |
rs142872496 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991068 | TGGAAATAAATTTGC[C/T]GCAAGAATGTTTCTA | 26259 |
rs142880455 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941205 | GCAGGATTGCCTGGG[A/C]CCCATTGGCCAGGGA | 26259 |
rs142895219 | snp | C/T | 0.000116145 | 0.00761965 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027399 | TGCCTTCCAGGCACC[C/T]GGTGCAGCACATCTC | 26259 |
rs142902441 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019126 | GAGACCTTTGTTTAC[-/A]AAGTCATCTTCAAGC | 26259 |
rs142909042 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003218 | CCAGCATAGCAGTCG[C/T]CTGTAAGGGGTAGAT | 26259 |
rs142911039 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958233 | GAGTTCATTTTGTTA[A/G]TTGCATAATACAACC | 26259 |
rs142959656 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963760 | GGAACTATGGCTAGG[A/G]CCTCAGGAAGACTAT | 26259 |
rs142961562 | in-del | -/GTTTGCA | 0.0232847 | 0.105357 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956520 | CGTCAGAGTGAGAGG[-/GTTTGCA]GTTTGCAGTTCTTTG | 26259 |
rs143034072 | snp | A/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978583 | TAATTGATCCTGTCT[A/G]TTTAACGATCATGAA | 26259 |
rs143038068 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007784 | TATGGCAATCAGATA[A/C]AATGAAGTCCCATTT | 26259 |
rs143124570 | snp | C/T | 0.000148264 | 0.00860872 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010353 | CTGGAAGCAGGACGC[C/T]GCCTCTTGAAGCTGG | 26259 |
rs143176794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966310 | TATGCAAAGATTGCA[C/G]TACTTTTAAGTTAGA | 26259 |
rs143179786 | snp | C/T | 0.000131846 | 0.00811822 | missense, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024290 | TGTGGGATTATCGGA[C/T]GAACCAGAAGCTGTG | 26259 |
rs143206274 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980454 | TTAAGCAAACCTTTA[C/T]TGATGTACAGCCACA | 26259 |
rs143228055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926924 | GTGCTTGGACTCCCT[C/T]AAAAACATTGAGGTG | 26259 |
rs143269776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019769 | CATGAATGAATTCTT[A/G]TTTTTTAAACATGGC | 26259 |
rs143272405 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961325 | TTTTTAAAGCATTCC[A/T]GGCAAATTTAATGTG | 26259 |
rs143305863 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917751 | TAATCCCAGCACTTT[A/G]GGAGGCCGAGGTGGA | 26259 |
rs143348141 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022776 | AAGTGCTCTCAGTGA[A/G]TGCTTTTGCCTTGAA | 26259 |
rs143373514 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941802 | TAGTATGCTATTTAA[A/C]TTTCTTTACTCTGTT | 26259 |
rs143385427 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029255 | AACCCCAAGACACTG[C/T]ACCCTATGGGCTATA | 26259 |
rs143385589 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020220 | ATTCCAGTTCATGAC[A/G]GCTAAAATGTGTCTG | 26259 |
rs143417252 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990419 | TCCTAAGGCAGTTTC[C/G]TTTCTCATGCTCTAA | 26259 |
rs143522004 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984561 | CTGAGCATCCCTAAT[C/T]CAAAATTCCAAAATG | 26259 |
rs143595117 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003226 | GCAGTCGCCTGTAAG[A/G]GGTAGATACACGCAG | 26259 |
rs143624418 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000008 | TTTTTTTTTGAGACG[A/G]AGTCTCGCTGTCTCC | 26259 |
rs143699803 | snp | A/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910079 | TCTCTTTCAGATTTT[A/T]AAAAAAAAATTTTTA | 26259 |
rs143701180 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999566 | CGCCCCTGCCCTTTC[C/T]CCACCTTTATACTCT | 26259 |
rs143734071 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955635 | AACAGCTCTTAGAAT[G/T]TTAGAATGTTTTGAA | 26259 |
rs143754925 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919136 | TATGGAAAGCAAAAC[C/T]GCGGATAAGGGGGGA | 26259 |
rs143760707 | in-del | -/CAAA | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909643 | AAAAACAAAACAAAC[-/CAAA]CAAACAAACAAACAA | 26259 |
rs143784934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963476 | GGACATGGTGGTGCA[C/T]GCCTATAATCCCAGC | 26259 |
rs143833995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950439 | TGGATCAGCTATGGA[A/G]TGAGACGCCTTAGGG | 26259 |
rs143905838 | snp | C/T | 0.000231149 | 0.0107481 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027445 | CCTCATCACGGCCAA[C/T]GTGCCTTACCAGACG | 26259 |
rs143930197 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960576 | TTTTTATTCAGTTTG[G/T]AAATAAGTGGAAGCA | 26259 |
rs143941875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000921 | GGAATGACACGAGCT[A/G]CGCTCCACCTAGTGC | 26259 |
rs143966751 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940144 | GATTTGTAACTGATG[C/T]TGTGGCCATGCCCAG | 26259 |
rs143975847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959105 | CATATGTTCTCCTGC[A/G]TCCCCTGAGAAGCAG | 26259 |
rs144038917 | snp | A/T | 0.00126854 | 0.0251528 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028125 | TGTGACGCCATGGCC[A/T]CTCACTACTACGACC | 26259 |
rs144048986 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923153 | AGAGGTTTCATTGAG[C/G]CAGGATCGTGCCACT | 26259 |
rs144049458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981051 | GGAGCTCTGTAACTA[C/T]CTGTTGAATGTATTA | 26259 |
rs144093776 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982973 | TACCAAGTCATGACA[A/T]AACAAGTGGCTTTGG | 26259 |
rs144111970 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936464 | TGGGGTGATTATCTT[A/G]GATTATACAGGTGGG | 26259 |
rs144112060 | snp | C/T | 0.000593198 | 0.0172118 | synonymous-codon, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985351 | CGTGATGTTATCCCC[C/T]AATGAGGAGGGGTAC | 26259 |
rs144131909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020372 | TTTTGTGTTTGATTC[A/G]TGTGCATTGAGTCGG | 26259 |
rs144165405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978246 | TTATGACCCTTGTCT[A/G]CACTGATACTAATCT | 26259 |
rs144183471 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952327 | TGAGTGTAACCCTGT[C/T]GTTTAGTGACACGAC | 26259 |
rs144206854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023820 | ACTGTGCTGGGCAGT[A/C]CACCTACTGCTGGGA | 26259 |
rs144244127 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981496 | AGTAATAACAATGTA[C/T]TTAAGGTTTACAAGA | 26259 |
rs144334258 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993428 | TTTTTAATAATGGCC[G/T]TTCTGGCTGGATAAG | 26259 |
rs144339819 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976261 | CTGACTTGGAGGCCT[A/G]AGATTAGATGGTACC | 26259 |
rs144392659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001760 | CCAGTCAGTCATACA[C/T]TTGCACGATGGTTAT | 26259 |
rs144470148 | snp | A/C/T | 0.0283406 | 0.115616 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952820 | TCAGCTCACTGCAAC[A/C/T]TCCACCTCCCAGGTT | 26259 |
rs144478244 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930553 | GGATATTAACTGCTT[A/G]TGAGATATATGGTTT | 26259 |
rs144524922 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992418 | TTTTTTTGAAGATCA[C/G]AGTTTTGTTTTTTTT | 26259 |
rs144534729 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028095 | CAGAGCCCTCTCCCT[A/G]TCTGCCGTTCATCCT | 26259 |
rs144540882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998637 | GGGAGTAAACACTGC[C/T]CAGGCATTGTTAGTG | 26259 |
rs144541283 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920878 | TCACAAACCCACTGT[G/T]GTTTCAAAAACCACA | 26259 |
rs144581730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925512 | CTTAAGATATGGACC[C/T]TCCGTTAGTGTATTG | 26259 |
rs144602646 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030946 | GTTTTTAGCCAATTG[A/G]TCCTCTACTTTCCTT | 26259 |
rs144611767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015660 | TCCAGTGTTTTCCCC[C/G]ATGGTCTCAAGTTTA | 26259 |
rs144672119 | snp | C/T | 0.000153988 | 0.00877328 | missense, synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945481 | TGCTGGAAGCTCATC[C/T]TCCAAGAGTGCCGAG | 26259 |
rs144681219 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940819 | GATCCTTCTGTGCAT[A/G]GGACTGCACAGCCCA | 26259 |
rs144750210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010697 | AAGCCATTTGGTGGC[C/T]GCAGTTGGTAGAAGG | 26259 |
rs144754927 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987375 | GGCGAAAGCCTGTTG[C/G]GAACGGCACCGCGGA | 26259 |
rs144787572 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935948 | TATATAGAGCTGACT[A/G]TGTATGTGCGAGGTA | 26259 |
rs144798593 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014391 | AAGTTCTTTAAAGTC[A/G]TTGAGGGTTCCCAAA | 26259 |
rs144857173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934096 | GAAACTCTGTTACTG[A/G]GAGGCCTTTGAGATT | 26259 |
rs144879761 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973388 | AAAATCTCCCCACTA[A/G]ACACTTACTAATTAA | 26259 |
rs144884698 | snp | A/G | 4.95683e-05 | 0.00497812 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945382 | AGCAAGACGTGGAAG[A/G]TGATTGCAGAGGATG | 26259 |
rs144911906 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021033 | GTGGTATTTGGTTGG[A/C]TATTGCCAAGTCACT | 26259 |
rs144987879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998993 | TTTATTAATTTCCTC[C/T]GCACTTCAGTCTTCT | 26259 |
rs144998028 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950861 | CTCCTTTCTACCCAC[A/G]GATGCTACAGTTTGG | 26259 |
rs145020610 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016672 | TCCTTTTGTCATTTG[C/T]GCTATGGATGTCATA | 26259 |
rs145025548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959084 | AAGAAGTCTTGCTAA[C/T]GGTTCCATATGTTCT | 26259 |
rs145051236 | in-del | -/TA | 0.084364 | 0.187256 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937721 | ATAGAGAGCTGTCTC[-/TA]TGTGGTGTGTCCTCC | 26259 |
rs145170560 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953485 | ATTTAAAAACAAAAG[C/T]AGCCGGCTGGGCGCG | 26259 |
rs145176998 | snp | A/T | 0.00154822 | 0.0277797 | stop-gained, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028112 | CTGCCGTTCATCCTG[A/T]GACGCCATGGCCACT | 26259 |
rs145219532 | in-del | -/CTGCCTCATTATGTACGCA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012166 | TTCCTCTGGAGCAAG[-/CTGCCTCATTATGTACGCA]CTGCCTCATTATGTA | 26259 |
rs145242451 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002315 | GAAATATCTTGGCCT[C/T]GTGGGCTTGTCACTC | 26259 |
rs145243322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970399 | AACACTCCCAGTGCA[A/G]CTGTCTGAACGCACA | 26259 |
rs145245164 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018118 | AGATGGATGCTCCTC[A/T]GTTGGAGTCTTTGGA | 26259 |
rs145245704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116974179 | TTGTGGGCCAGAGTA[C/T]TGGGGAAGAGGGAGC | 26259 |
rs145275925 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913020 | CTGGGGATTGAATTT[A/G]GATCCAGGTCTTTTC | 26259 |
rs145290928 | in-del | -/TGGTAA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929857 | TGCCCCGCCAGCCAC[-/TGGTAA]CCGCCATTCTACTCT | 26259 |
rs145304670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954777 | CAGCTTCTTTGCAAT[A/C]TAACCTTTTGACTTG | 26259 |
rs145344777 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977357 | TCTGAGAAGACACTT[A/G]GTCTGCAGTGTGGCT | 26259 |
rs145344843 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927341 | TAATAAATGACACCG[A/C]AGAAGAACTGCTTTG | 26259 |
rs145380955 | snp | C/T | 0.000462 | 0.0151917 | synonymous-codon, stop-gained, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024159 | CAGGGTGAGGATCCA[C/T]GACCTCCGCAGTGGT | 26259 |
rs145388883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013492 | GCAATGAGTAATGGT[A/G]CGGGGAGTGATGCAC | 26259 |
rs145399216 | in-del | -/T | 0.0263992 | 0.111815 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969841 | CCTGGGGTGTTGAGA[-/T]TTGGCAAGGTGATCC | 26259 |
rs145405264 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949657 | CTGGAGCATGTTCCT[C/G]ACACAGTTTTGTGTG | 26259 |
rs145425875 | in-del | -/T | 0.0422008 | 0.138995 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960848 | GTATTAGTAAAAGCA[-/T]GTTTCTTCAGATAAA | 26259 |
rs145437071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025966 | CCTCTGTCCCTGTGC[A/G]GTCCAGGCTTGTCCC | 26259 |
rs145470547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983688 | GGTCTGTTCTAGATA[A/G]TAGGAAGTTATAGGA | 26259 |
rs145521304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116974862 | ATAAATACAAGATGA[A/G]TCTGGAACATTTTAT | 26259 |
rs145526488 | in-del | -/CTA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116942768 | TTAACTCCAGAGCTT[-/CTA]TTTTTTTTTTTTTTT | 26259 |
rs145533793 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920046 | GAATTGACTTAACTG[C/G]AATAACTTCCTTTCC | 26259 |
rs145572236 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977997 | CTATTTTGGTGATCT[C/T]GCTGCTTTGTTTATG | 26259 |
rs145611058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931667 | ATTTCTTTTACAGAT[A/G]GCTTGTTGTTAGTAT | 26259 |
rs145640934 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032556 | AAAGCGTGGTTACCT[A/C]GCATCAGATTCTCCA | 26259 |
rs145642603 | snp | C/T | 0.0209421 | 0.100162 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910033 | CTTCTGGAAATCTCT[C/T]TCCTAAGATCTGACC | 26259 |
rs145735897 | snp | A/G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030257 | AAGCGTCACCTTCCC[A/G/T]TCCAGAGCGCTTTCT | 26259 |
rs145748551 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932599 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 26259 |
rs145789472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994342 | TGTAAAAGTAAATAC[A/G]TAGACCAATGGAACA | 26259 |
rs145823135 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949687 | GATGTGCATTCTCAC[A/G]ATGGTGTGGTCATTG | 26259 |
rs145835478 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990086 | CAAATCTCATTTATG[C/T]AGGTGTGATTGGCTT | 26259 |
rs145857670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927231 | TTTCTTTGTGCTACC[A/G]GGATCGTCAATGACA | 26259 |
rs145864448 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005155 | TTGGGTAGGATGGAG[A/C]AGTTCCTTTGTACAT | 26259 |
rs145867277 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995581 | TTCCTCAGTTCCTAC[A/G]TCTTGCCTTGTAAGC | 26259 |
rs145868955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916788 | TAGCTCACCATTTTG[C/T]AGGGTGGCAGCTTGG | 26259 |
rs145895312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942523 | GGGATTACAGGTGCA[C/T]GCCACCATGTCCAGC | 26259 |
rs145963984 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923261 | AGGGCAGTAGGTCTT[G/T]GTAGGGCCCTTGGCA | 26259 |
rs145965165 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971704 | ATTTTTTTAAATCTG[C/T]GCTTTTGTTTTTATG | 26259 |
rs145966270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002710 | TAAACTGCTTTTAAA[C/T]CAGACATCCATTATT | 26259 |
rs145972801 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925137 | GAGATTTGCATGTAG[A/G]TGGTTTAGTGGGTTT | 26259 |
rs145984346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926352 | AAGTAGGTAAAGTAG[A/G]CCTCTCCACAATGTC | 26259 |
rs145992107 | in-del | -/AAAAAAA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009847 | AAGCATCCAGTGGCT[-/AAAAAAA]ATGCAAGCTTCATCT | 26259 |
rs145995151 | in-del | -/ATAA | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914925 | ATTAGTAACACTGCT[-/ATAA]ATAAAGTTATAATTC | 26259 |
rs146007256 | snp | C/G | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987911 | GTGTACTTTCTCCAC[C/G]CCCACCTTGTACACA | 26259 |
rs146084480 | in-del | -/T | 0.00993419 | 0.0697739 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919687 | GGGGCCCTATCTATG[-/T]TTGTTGAGTTGAAAT | 26259 |
rs146087380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941293 | TCTTGATTCTTCAGG[C/T]TCTAAACCACTGGAG | 26259 |
rs146127058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004318 | TTGTATTCTTTATTT[A/G]ATCTTGCCTGGAAGT | 26259 |
rs146205632 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008003 | ACATTTTAGAAAATA[C/T]TGGACTCTGGACTAC | 26259 |
rs146206230 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963373 | ACACTTTTGGAGGCC[A/G]ACGTGGGTGGATCAC | 26259 |
rs146225684 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966751 | ACAGGGTTTTGCTGT[A/G]CCACCCAGGCTGGAG | 26259 |
rs146249417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946432 | TAGTGACATTTGGGG[A/C]CAGCTAATTCGTTTT | 26259 |
rs146260163 | in-del | -/GGGG/GGT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117006519 | CCGCCTGCCCACGGC[-/GGGG/GGT]GGTGGCTGATGCCTC | 26259 |
rs146326522 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027280 | CCCTCTGTGAAAGAG[A/C]AGCTTAGCTTTATGG | 26259 |
rs146328546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951806 | TCTCCTTTTCACATA[A/G]AACCAGTGAAATCTG | 26259 |
rs146370409 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967352 | AAACAGTGCTGCAAG[A/C]AATATACTTGAACAA | 26259 |
rs146438472 | in-del | -/GAG/TAGAG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021586 | GAGAAAATTATTATA[-/GAG/TAGAG]GAGTATTTTGCCTCT | 26259 |
rs146475392 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982990 | ACAAGTGGCTTTGGA[C/G]CAAGTTGTTTAACCG | 26259 |
rs146495575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928398 | TGCTGGTGGCCGACA[A/G]CTTGGTGCTAAGCCT | 26259 |
rs146513476 | in-del | -/A | 0.114738 | 0.210248 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014263 | CATATTTTCTTGGTT[-/A]AAAAATTTCCATTTG | 26259 |
rs146592680 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001903 | AAAATGATCCCAAAG[A/C]AAAGAGAGAACCATA | 26259 |
rs146630044 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921078 | ATTTCCCCCAGCACT[G/T]GCATTTCTTTAGATT | 26259 |
rs146635166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998906 | TTTCAAAATACACAT[C/T]GCAGCTTAGACTCAC | 26259 |
rs146662313 | in-del | -/TTTG | 0.0337553 | 0.125452 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010757 | TCCCCTGCTGCAAAA[-/TTTG]TTTGGCACTTGAAAG | 26259 |
rs146667375 | snp | A/C/G | 0.000795439 | 0.0199275 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010391 | TCTCCGTGACTTCAC[A/C/G]TGTGTCAACCTCAGC | 26259 |
rs146711441 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020221 | TTCCAGTTCATGACA[A/G]CTAAAATGTGTCTGA | 26259 |
rs146750027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938946 | TGGGATCTCTGTCAC[A/G]TGCCAAAGGTTTTGG | 26259 |
rs146753683 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017678 | AATTAATTTGGTCAT[A/T]AAAAAAGCCTACATT | 26259 |
rs146768769 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941995 | ACAGGCCTCTGAGGC[C/T]CTGTTCATTTTATTC | 26259 |
rs146786873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943838 | TAGCAGTGCCTCCTC[A/G]GGCAGCTGTAGAGTT | 26259 |
rs146787832 | in-del | -/GTTGGAAAGC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116974489 | GATCCCCTAAAAAAA[-/GTTGGAAAGC]AAGCCACAAAAGGAT | 26259 |
rs146791294 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030851 | TGACAGGGAAAGGAT[-/A]AATGCTCCTTTATAA | 26259 |
rs146834293 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963496 | ATAATCCCAGCTACT[G/T]GGGAGGCTGAGGCAG | 26259 |
rs146853754 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920412 | ATATAGCATTGAACA[A/G]GGCAGAAAAAAGCCT | 26259 |
rs146875548 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032457 | ATTTTTTTCTCAATG[G/T]TATAACAAAATGACA | 26259 |
rs146877316 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960579 | TTATTCAGTTTGGAA[A/G]TAAGTGGAAGCAGTC | 26259 |
rs146948918 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026008 | CTGTTTTCACCAGCA[C/T]AAGGCTGACAGACAC | 26259 |
rs146950310 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949121 | GAAATAGTATCATCT[C/T]ATCTCCTTTTCCTCA | 26259 |
rs146986276 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965769 | TACATACATACCTAT[A/G]TATATTTGAGACAGG | 26259 |
rs147055273 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921692 | ATGTGTTGCTTTTCT[G/T]TGTCTGTGAAAATAT | 26259 |
rs147055327 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969304 | CTCCCCTCTCATGCT[A/G]AGCTTGTTTCATTGG | 26259 |
rs147108147 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022905 | TGGGCAGCTCTTCTT[G/T]TTAATAGGAAGGTTT | 26259 |
rs147127683 | snp | C/G | 0.00438332 | 0.0466095 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031308 | GAACCTCCCCTACAG[C/G]CGCTCCCAGCCCAGG | 26259 |
rs147133915 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014716 | TTTCTATGCTGTTTT[-/T]GGTCTGCGCATGTGC | 26259 |
rs147144324 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993129 | TTTTTTTTGAGATGA[C/T]GTCTTGCTCTGTCGC | 26259 |
rs147209974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919603 | CTTAGCTTCCGCCTC[C/T]TGTGAATCCCTGGAG | 26259 |
rs147213052 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997877 | CCAGAGTGCAGTGGC[A/G]CCATCTCAGCTCACT | 26259 |
rs147231081 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921930 | CCTCCCATACTCAAG[C/G]TATCCTCCCACCTCA | 26259 |
rs147249982 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010036 | TCTTTGTTAAGAAAT[C/T]AGAATACCTGATTTC | 26259 |
rs147289806 | snp | C/T | 0.00153584 | 0.0276688 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985400 | TTTGAAGTTCCGAAA[C/T]TGGTGAGCTTTTTAG | 26259 |
rs147303830 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011198 | AGGTAGCATGGCTGA[A/G]GGCCAGGGGCTGCTG | 26259 |
rs147320126 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015423 | TTTCTTTTCAGTGAA[C/T]TAAGTCAGCACAGTA | 26259 |
rs147321157 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936563 | GGCCTTGAAGGTGGA[A/G]GAAGGGGCCACAAAC | 26259 |
rs147337910 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116940150 | TAACTGATGCTGTGG[C/G]CATGCCCAGGGTGGG | 26259 |
rs147342155 | snp | C/G | 0.030665 | 0.119967 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998074 | TCCGCCTTCCTTAGC[C/G]TCCCAAAGTGCTGGG | 26259 |
rs147371907 | in-del | -/GCTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018603 | CTGTTTCTGTCGACG[-/GCTT]AGAAGCCAGAGTGGT | 26259 |
rs147409132 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116940581 | TACTGTTGCGAGGAA[A/G]AGAATGTGAACGGTG | 26259 |
rs147427863 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958652 | GGTTGGGGAGGAGCA[C/T]GGTGCCATAACATGC | 26259 |
rs147443590 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961676 | CAGACCCTGAGCTCA[A/G]AAGCTTCAGGCTGGT | 26259 |
rs147447055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016336 | CACTTGCTACAGTCT[C/T]GAATTCTAGATTTGC | 26259 |
rs147449897 | snp | A/G | 0.00226306 | 0.033562 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027419 | CAGCACATCTCATTC[A/G]GCAGCCACAGCCTCA | 26259 |
rs147459619 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985278 | ACGATGCAAGAATAC[A/G]GGCACTAGCCCTCAG | 26259 |
rs147460824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019846 | TCTCCAAGGTAATTG[C/T]TGTTAATGTTTCAAG | 26259 |
rs147530283 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116976905 | ATTTCAGGGGGTAAT[C/G]AAAAAAGTCTGAAGA | 26259 |
rs147542337 | in-del | -/T/TT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992426 | AAGATCAGAGTTTTG[-/T/TT]TTTTTTTTTTAATTC | 26259 |
rs147546511 | snp | C/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980651 | ACCTATTTGAGAAGT[C/G]AATTTCCTTGACCCT | 26259 |
rs147549342 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989843 | CCCTCTTTATGCCTC[A/G]GTTTCCTCATTTGTA | 26259 |
rs147563472 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913197 | AGTTTAAGACATTAT[A/G]CTCTACTGTATAGCC | 26259 |
rs147575784 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954717 | AGGGGAATGAATTTT[-/T]ATTTTCCAGATTAAT | 26259 |
rs147585737 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984845 | TAAATTAAAAATTAG[C/T]TGGGTATGGTGGCAC | 26259 |
rs147585785 | snp | C/T | 0.0016457 | 0.0286381 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028223 | GAAGAACCAGTTTTA[C/T]CCATCTTAAAACGCC | 26259 |
rs147623777 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969451 | TACACTAACATTTTC[A/G]TGAATAGCTACTTTT | 26259 |
rs147656905 | snp | C/T | 0.000382374 | 0.0138218 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928037 | GAATGAAATGAATGA[C/T]GTGCCTTTCTTTGAT | 26259 |
rs147672874 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931943 | CTGAAGAAAAGCTTT[C/G]AACTTTTTACTAAGT | 26259 |
rs147728169 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990189 | ACTAAGCGGTAGACG[A/G]TATGTGTGGCATCCT | 26259 |
rs147760258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947403 | TATCTTTCATTAAAT[G/T]TAATGGTGGGATTCT | 26259 |
rs147777724 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953022 | GGATTACAGGCGTGA[A/G]CCACTGCACCCGGCC | 26259 |
rs147796737 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993657 | TTAGTCCTTTGTTGG[A/G]TATATAGTTTGCAAA | 26259 |
rs147833285 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007174 | AAAGATTTTTAGAAA[C/T]AGATTTCAGATACAT | 26259 |
rs147866134 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968475 | CTGTGTAGAGAGAGT[A/C]CCCCGTTTGCACACC | 26259 |
rs147882872 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973553 | CAGAATCACTTCTTT[G/T]ATATTATTCCAGCCA | 26259 |
rs147900742 | in-del | -/G | 0.0119091 | 0.0762411 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023545 | GGTTCTTAAAGAAAT[-/G]GGGGATTATTATAAG | 26259 |
rs147903222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011651 | TGAGCTATACAGAGG[C/T]TCCAAGCTCCTCTCC | 26259 |
rs147920835 | in-del | -/TG | 0.0513262 | 0.151752 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994822 | CTGGTGTTTTGCTAT[-/TG]TGTAAACAACACTTG | 26259 |
rs147936900 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026148 | CCGCTTCAGTCTCTT[C/T]AGCCCAGGTCCTCGC | 26259 |
rs147968895 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956117 | CTCTCTTTTGGTTTT[-/A]AAAAAAACACCAAGC | 26259 |
rs147989371 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003300 | TATACTGAGCCCCTC[C/G]TATGTGCCAAACACT | 26259 |
rs147989576 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926012 | GTGATGCCAAGATAC[A/G]GGCATTGTCTTCCAT | 26259 |
rs148041386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999801 | CCAGCGCCATCCTCA[A/G]TGTGCCACATTCATT | 26259 |
rs148110303 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956637 | CCCTTCAGTGGAATT[G/T]TATCATTGTTTTACA | 26259 |
rs148131435 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014538 | CATTGTGGATGTTGT[A/G]TTTTATACACTCTGG | 26259 |
rs148169235 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026636 | CCTCCTGCTCCTCCC[A/T]GCACTTAACTCTGGG | 26259 |
rs148181318 | snp | A/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979209 | TTTACAAAAGCTAAC[A/T]TAAATCAGTTTAAAC | 26259 |
rs148200865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966492 | TCCAGGGCCGTGCTG[C/T]GGTGGTCGTGCTGTT | 26259 |
rs148269991 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969348 | TTACTGTTTCTGTGA[-/T]TAAACAACAACTTCT | 26259 |
rs148270414 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922365 | GAAAGTTGAGATAAA[C/T]GCCTAAAGAAACTAG | 26259 |
rs148323436 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028974 | AGCAACAGCATCCAC[C/T]TAATATACCTTCAGA | 26259 |
rs148324700 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917863 | CGGGTGTGGTGGCAC[A/G]TGCCTGTAGTCCCAG | 26259 |
rs148326972 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996138 | ATATTTCCTAATTTA[G/T]GTCTGAAGTACTTGG | 26259 |
rs148339262 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943841 | CAGTGCCTCCTCAGG[C/T]AGCTGTAGAGTTAAG | 26259 |
rs148374666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990440 | CATGCTCTAAAAAAA[C/G]TTTCTTTTCCCATCC | 26259 |
rs148423329 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927199 | ACACTTGGCTTTTTT[-/T]CTGTTTCACACTCAT | 26259 |
rs148430304 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998214 | AGCTAATGTGAATGC[C/T]GTCACTTCATATGAA | 26259 |
rs148446419 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946508 | GGCCTCTCCCCATTA[A/G]ACGCCAGTAGCATTC | 26259 |
rs148481985 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992595 | GGTCCTCCAATACCA[C/G]TCTGTGCCTCTGCAT | 26259 |
rs148503427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019912 | GGTTTTATTTAAACA[A/G]GAAGTACGCACATTC | 26259 |
rs148518305 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005926 | GTGCCTCTTCTCTTA[C/T]ACTCCACTCAGCCCA | 26259 |
rs148567766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972288 | AAGTTCTTAAGTGTA[C/T]CTAATGACAACTGAG | 26259 |
rs148572734 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001548 | ATTTTCAAAATAGTA[C/T]GCAAGTTGCCTTTAA | 26259 |
rs148574295 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028086 | CTGGCCTTCCAGAGC[C/G]CTCTCCCTGTCTGCC | 26259 |
rs148640923 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959596 | GCTGCTGGATACTTA[C/T]GAAGAAGAAAGGTTG | 26259 |
rs148663293 | in-del | -/CT | 0.0566069 | 0.158427 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029410 | AAAACAAACTATAAA[-/CT]CTCTAGACTGGGCTG | 26259 |
rs148691969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027576 | CCCCACCCCCCCCGC[C/T]GTGACACATTGCACC | 26259 |
rs148692564 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952572 | CGGAACTCCTAGAGA[C/T]GGGACCATCTACAGC | 26259 |
rs148707572 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981770 | AGGTGCCCACCACAA[C/T]GACTGGCTAATTTTT | 26259 |
rs148730476 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968174 | ATTTTGTAATTTAAT[A/G]TTTTTGATTACTACA | 26259 |
rs148744552 | snp | C/T | 0.00031969 | 0.0126389 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024109 | AAGCTTTGACTCTAA[C/T]CCCATTTCCCTTCTC | 26259 |
rs148772767 | in-del | -/TTGAA | 0.0437281 | 0.141251 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009607 | GTTCTTTGAATTAAG[-/TTGAA]TTGAATTAATACTTT | 26259 |
rs148779705 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930857 | CTGTTGCCCAGGCTG[G/T]CATGCAGTGGTACAA | 26259 |
rs148779892 | snp | A/C/T | 1.64947e-05 | 0.00287177 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988665 | TACCTTTTAACAGGT[A/C/T]CAGTACCTTGAAATA | 26259 |
rs148796515 | in-del | -/GT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992762 | GAGTATTATTCCATG[-/GT]GTGTGTGTGTGTGTG | 26259 |
rs148820242 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984226 | TGGAAAAGCATAAGC[G/T]CCTGTAGACCACTGG | 26259 |
rs148836801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939100 | TCTGCAGAGCACTGG[A/G]CTTTTGAGATACTCG | 26259 |
rs148956109 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921631 | AGCACCTGGTGTGGC[C/T]CTGAATTTAGATAGT | 26259 |
rs148958336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999338 | GAACTGTGCCAGGGA[C/T]GTGGGATGACCGACT | 26259 |
rs148977655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950399 | TGCCATAAAGTAGAA[A/C]GCAGAACACTTAAAT | 26259 |
rs149001995 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965776 | ATACCTATATATATT[-/T]GAGACAGGGTCTCAC | 26259 |
rs149012758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995085 | GTCCTGCCCTTCATT[G/T]AAATTATTTTTCAGC | 26259 |
rs149027096 | in-del | -/GTGAA | 0.0146672 | 0.084371 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965536 | ATCCTCCGTTATGTT[-/GTGAA]GTGTTGAATCTCCAC | 26259 |
rs149027442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021212 | CTGTGTAATTTATCT[C/G]ATTACCAGCAAACTT | 26259 |
rs149028870 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942410 | GACAGAGTCTTGCGC[A/T]GTTGCCCAGGCTGGA | 26259 |
rs149040764 | snp | C/T | 0.000527574 | 0.0162329 | synonymous-codon, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945411 | TGAGGTGCTGTGGTA[C/T]AGGCTGTGCCAGCAG | 26259 |
rs149079220 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017006 | ATGTCTGTGTTCTGG[C/T]ACTACCACGCTGTAC | 26259 |
rs149096197 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116974339 | ATTCCTGGAGCTCAC[A/T]TGAGGCTAAGAATAG | 26259 |
rs149140974 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116999634 | GTCCACTTCAGGTTT[-/T]CTCAGAGCACTGGCT | 26259 |
rs149154296 | in-del | -/C | 0.0517044 | 0.152246 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015753 | GTGTTTTAAGTAGGT[-/C]CACAAGGTTGTGCAG | 26259 |
rs149171262 | snp | A/C | 0.0707826 | 0.174302 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961274 | AAAGTGCTGGGATTA[A/C]AGGCATGAGCCACCG | 26259 |
rs149185491 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990321 | GGTTGGGGCATCTCC[A/G]TTGTGTCCTAGCTGG | 26259 |
rs149221566 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923837 | GCCGTTCTTCTACTT[A/G]AGCCTCCTGAGTAAC | 26259 |
rs149222502 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028589 | AGGGCCTTTGGATGT[A/G]CTTGTTCCTGGCCTC | 26259 |
rs149260642 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975544 | AACATTCAGATGAGC[A/G]ATGAGTAACAGGACA | 26259 |
rs149294770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992137 | TTTCTAAGGAAACAA[A/G]GCCGAGTAATTTAGC | 26259 |
rs149329255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925444 | ATTACTCTAAGTGTG[C/T]GGCATGAAACTTGAG | 26259 |
rs149333840 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030680 | CAAGTGTAGCCCCTC[A/C]CACCGCAGAGCCTGT | 26259 |
rs149350073 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986871 | AACACGGAGATAAAG[C/T]TAAAGGGCTAGACGG | 26259 |
rs149415291 | snp | C/T | 0.00405517 | 0.0448458 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028046 | CCGGGGGCTGATCCG[C/T]GCCTATGAGTTTGCG | 26259 |
rs149420525 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940574 | TTGGGGTTACTGTTG[C/T]GAGGAAGAGAATGTG | 26259 |
rs149471484 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014146 | CTTTCTGTTCTTCAG[G/T]CTGCATCATCTCCGT | 26259 |
rs149473221 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935892 | GCAATGCTAATTTTT[A/T]AAAAAAAGTTGGACT | 26259 |
rs149493671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000904 | GGTCACAAAGTGGCG[C/T]AGGAATGACACGAGC | 26259 |
rs149508699 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951857 | AACGCATTTGACACT[C/G]AAATACCCATCATGT | 26259 |
rs149526396 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007753 | GTGTGAGCATGAATA[A/G]TTAATCTCACTAGTC | 26259 |
rs149537229 | in-del | -/GG | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916897 | ATTGTGCGTGTGTGT[-/GG]GTGTGTGTGTGTGTG | 26259 |
rs149542596 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966092 | ATATTTTATATAATT[A/G]CTTTAGCAACGTGAT | 26259 |
rs149545493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997852 | ATGGAATCTCATTCT[A/G]TCACCCAGGCCAGAG | 26259 |
rs149556920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945738 | AGATTTGGGAACATC[C/T]TCTTATTCTGCAGGA | 26259 |
rs149559262 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917471 | CTTCCTCCCTGCCCC[C/T]GTTTCTTCTCCAACC | 26259 |
rs149559506 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023668 | TCAGTTCCAGCAAGA[C/T]AGCAATGAACTTACA | 26259 |
rs149631040 | in-del | -/T | 0.0517044 | 0.152246 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026509 | GGAGGCAGGGACTGC[-/T]TTCCCAGCTTCCCTC | 26259 |
rs149656040 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116918974 | TGCCATGTTTTTTTT[-/T]CCTATATACACAGAG | 26259 |
rs149665753 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919729 | AATTGCTGCTTCTGA[C/T]TGCGACTTTATAAAG | 26259 |
rs149669551 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025596 | GGGCAGTGTTGGCAA[A/G]CACTGTGGCCGGCAC | 26259 |
rs149738726 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983366 | GAACCTTTTGTGATC[C/T]GCTTATCCCCCAAGT | 26259 |
rs149790289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977977 | CTCTTCTCTTGACTC[A/G]GTTTCTATTTTGGTG | 26259 |
rs149807180 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932598 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 26259 |
rs149827895 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994144 | AGTAATAAAAACAGC[A/G]TGGTACTGGTGGTAA | 26259 |
rs149859171 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004977 | AGGACTGTTTGATGA[C/T]AGGCTGAGTCTTATC | 26259 |
rs149864321 | snp | A/G | 0.0174175 | 0.0916809 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032372 | TGGGAGGAAACCAGA[A/G]TGCCCAGAAAGCTCT | 26259 |
rs149880244 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989550 | GAGCCAAAAGCAGGA[A/G]GACAGGTTTTTAATG | 26259 |
rs149905438 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924175 | ATGTTTTTAAGTCAG[-/T]GTTGTCCATTTTCAT | 26259 |
rs149949742 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942155 | TGCCTCAGTCTCACA[A/G]GTAGCTGGGACTACA | 26259 |
rs149997794 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938429 | GTGACCCGGGGTTAG[C/T]GATGTGAATGATGCA | 26259 |
rs150000082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016390 | TTAACATCCTTTCAC[A/G]TGCTTATTGCCTGTT | 26259 |
rs150036359 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028236 | TATCCATCTTAAAAC[A/G]CCAGGCACCTCTTCA | 26259 |
rs150054650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009923 | TTCAGATGAGAACTC[A/G]TGCTGGCTCATCTGC | 26259 |
rs150071158 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967770 | GTAAGTCACTTATTC[C/T]TTTTTGTTTGTTTTG | 26259 |
rs150102094 | snp | A/G | 0.0134861 | 0.0810011 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909131 | TCGCACTGTCGCCCA[A/G]GCTGGAGTGTAGTGG | 26259 |
rs150105111 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939703 | TGTGTTTCCTGAGCA[C/T]GTTCTGCCTTTGAGA | 26259 |
rs150110507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018633 | TGCTTCTCTAAGGAG[A/C]TGTCAGAAAAATGTT | 26259 |
rs150162104 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013072 | CAGATGGTGAAACCC[C/T]GTCTCTACTAAAATA | 26259 |
rs150179211 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970072 | TGCTAATGCAGGGAC[A/G]GCGGAGACCTTGCCA | 26259 |
rs150198818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026965 | AGCAGGATGTGGGGG[A/G]CACCTTCATGGATCA | 26259 |
rs150220170 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116972042 | AATTGAAATATTTTT[-/T]CTCCTGTAGAAAAAT | 26259 |
rs150227236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965062 | TGGAACACAGCACCC[A/G]TTAAAACTGGTGTTT | 26259 |
rs150266796 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985811 | CCCAGTCCATCTGGG[A/T]AGGAAGGTTTCCATT | 26259 |
rs150314746 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979814 | TTGGTTTCTTGGCAG[A/G]GGCATAAGAAGCAAG | 26259 |
rs150378163 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012298 | TGTTACATTTTTTTT[-/T]AAAACGCTCTGTCTC | 26259 |
rs150383087 | snp | A/T | 0.0509478 | 0.151255 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929116 | CGGCCCCATTGATGG[A/T]CTGCTTTCTAAGCAG | 26259 |
rs150404493 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960825 | GGAGACGATCAATGC[A/C]TAAGGACTGTATTAG | 26259 |
rs150432450 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116931459 | TTGCATTTCACTCAC[-/T]TTTGAGTAGTATGGA | 26259 |
rs150441635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002220 | GGGGTTGCAGGTGCA[C/T]TGGCACGTGGTGGTG | 26259 |
rs150510778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962465 | TTTCCTCTCCACCCT[C/G]GCCTCCCCACTGTGT | 26259 |
rs150541038 | in-del | -/CTTT | 0.0832709 | 0.186283 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934956 | AGTCCTTCCCCGACC[-/CTTT]CACCCCCAGCTCCAT | 26259 |
rs150547266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003377 | GGCGCACCCTGGGCA[C/T]CTGGCATCTTCCATG | 26259 |
rs150562621 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957240 | TAATCTCAGCTACTC[A/G]GGTGGCTGAGGCACA | 26259 |
rs150568749 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030547 | TCAGTCTGCGTTCCC[A/T]GTTCATTTTGCAGGC | 26259 |
rs150595593 | snp | A/G | 1.65266e-05 | 0.00287455 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964793 | GGATGAGCCTGGAAT[A/G]CAGCCAAATGTCTCC | 26259 |
rs150631436 | snp | A/G | 0.0209421 | 0.100162 | intron-variant, synonymous-codon, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116911340 | GCAGCTGGTGGACCA[A/G]CTCATCCGCGACCTG | 26259 |
rs150639496 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020005 | TGTCAGCCTCCCTCA[C/G/T]TGCGACTGCTTAAAT | 26259 |
rs150656115 | in-del | -/A | 0.0517044 | 0.152246 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018954 | ACCAAATATGCACTG[-/A]AAAAGTACTTGGTAA | 26259 |
rs150668326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926963 | TTTGTTTTGAGACAG[C/T]AGCCTTGCAATACAT | 26259 |
rs150703363 | in-del | -/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117024076 | ACCAGCACCGTGGAG[-/G]GGGGAGTTTGTCATT | 26259 |
rs150704057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973228 | TATAGTAGAATGTCA[A/G]CTAATAAATGCAGAA | 26259 |
rs150714743 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943239 | GACTGCCTTTTCCCC[-/C]TGTGTATGGGCCCTG | 26259 |
rs150719207 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922571 | TCTTAGTAATTATCT[G/T]TTCTTCTATTAAACA | 26259 |
rs150723671 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027907 | GTGTGCCCAGAGAAC[A/G]CGTTTGTGAAGCTGA | 26259 |
rs150724702 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000717 | GGTTTGAGCTCCTTA[A/G]GGCCCCATATTCTCC | 26259 |
rs150776814 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996308 | AAAATCATTGCTAAC[A/G]TCTCTTATGATAATT | 26259 |
rs150862692 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936959 | GCTGTGTGGAGAATC[A/G]GTTGTTGGGGGACAA | 26259 |
rs150882047 | snp | G/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976639 | TTTTTTTTTTTTTTG[G/T]ATTTTTATTAGAGAT | 26259 |
rs150896242 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945258 | AATGAGACATTTTAT[A/G]CTGCCATAAACCCAG | 26259 |
rs150930688 | in-del | -/GGGTG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959045 | GGTTTGGGAGTGGCT[-/GGGTG]GTTTGTGTATGATCC | 26259 |
rs150951961 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953982 | AGCTGGGCGTGGTGG[C/T]GGGCACCTGTAATCC | 26259 |
rs150967720 | snp | A/C | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028146 | TACTACGACCTCGCA[A/C]TGGCCTTTCCCTATA | 26259 |
rs150975971 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012619 | TTTAATAGCTATGAG[G/T]AAGATCTCATTAGAG | 26259 |
rs151003700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946638 | AGAGTTAGTGTGGCT[A/G]TCCTTTCTTAGGCTG | 26259 |
rs151009621 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025382 | CTGAGCATGACAACA[C/T]AGAAGAGCAGAAACA | 26259 |
rs151024377 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006047 | AATGCTATTGTCTTG[G/T]AAGGAAGCCTTCCGA | 26259 |
rs151041162 | snp | A/G | 0.000313389 | 0.0125138 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964660 | TAGCCCTGCTCTTCA[A/G]TCTCCTTTTGGAACC | 26259 |
rs151093850 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960245 | TGTTTTACCCTACCA[A/C]AGATGTCTGTTTCCT | 26259 |
rs151098910 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031926 | GAAAAATTACTAAAA[A/G]CAAGATAATTACCCA | 26259 |
rs151111194 | in-del | -/ATTT | 0.0146672 | 0.084371 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957809 | TAAAAATACTTTTAA[-/ATTT]ATTTATTTTCTGCTG | 26259 |
rs151163667 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914248 | ACTGCACTCCAGCCT[A/G]GGTGACACAGCAAGA | 26259 |
rs151167534 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021887 | TCATCCCGTTGCTTT[C/T]GGCTTCCATGGACGT | 26259 |
rs151188000 | in-del | -/T | 0.0584853 | 0.160693 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021745 | CCCACTTCTTTCCGA[-/T]TTTTTTTTAACCTTT | 26259 |
rs151190024 | in-del | -/CTAT | 0.00755907 | 0.0610114 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972896 | CTGTTGAAAGTATCA[-/CTAT]CTACTAAAAGGAACC | 26259 |
rs151199248 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928559 | TGAAGTCATGTTTTA[A/G]GTGTATAGTCCAAAT | 26259 |
rs151216763 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988365 | TTTTCCCTCCTTCAC[G/T]TCCAGCCCAGGGTGT | 26259 |
rs151254283 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924104 | CTAATGTCTTTAATT[A/C]CTTTTCCTTCTTCTT | 26259 |
rs151256339 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002039 | TTTGTACCCGAGTGT[A/T]CTCTTGCTCTGTGGG | 26259 |
rs151304396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998500 | TTCCCTGATGGTTTA[C/T]GTGGAATTGCCTTCC | 26259 |
rs151338590 | snp | A/G | 0.000214166 | 0.0103459 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988759 | AAAGCCGAAGACTCC[A/G]CCAGAACCCTCCTTT | 26259 |
rs180697232 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913722 | GTTTATGGAAAAAAC[C/G]TGCATACAAGTGGAC | 26259 |
rs180713302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930314 | CCCTTCTCTCCATGT[C/T]TTTGCCAGCACTTGT | 26259 |
rs180717121 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950432 | CTTAGTTTGGATCAG[C/G]TATGGAGTGAGACGC | 26259 |
rs180847927 | snp | C/T | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946715 | TTTTCCATCCACCTA[C/T]GGTAATAAACTCGTC | 26259 |
rs180880779 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954494 | TGTATGTTATGAATA[A/T]TTTATGTATAGATGT | 26259 |
rs180912778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027647 | AATTGGAAACATAAA[C/T]GTGGATGCTGACCTG | 26259 |
rs180921559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116918750 | AGCTCTGCCTAAATT[A/G]TGTTGACTAAGAGTG | 26259 |
rs180925222 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008467 | AGAAATTTTTCTTTT[A/C]AACTGCAATTGTTCT | 26259 |
rs180929965 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988573 | TTCTGTTGGGTTGCT[A/G]GTCTTCTCATTGATG | 26259 |
rs180932935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967699 | TGTCATCTTTTCTGG[C/T]TGAAAAGAAAGCTTG | 26259 |
rs180950846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927735 | ACCAGGCTGGAAGAT[A/G]GCACCCCTGCTGCTT | 26259 |
rs180974759 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935834 | TACGGAGGGCAGCAC[A/G]TGCCAGGAGCTGAGC | 26259 |
rs180978011 | snp | A/C | 0.0379877 | 0.132479 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909479 | CTAAAAATACAAAAA[A/C]TTAGCCAGGTGTGGT | 26259 |
rs181103845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927324 | CTCTGATTTCTCTGC[A/G]TTAATAAATGACACC | 26259 |
rs181111889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017587 | ATTTAAAATCCTCTT[C/T]AATATTTAATAGCCC | 26259 |
rs181126589 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000518 | CACCCCCGGAGCTTC[C/T]GACTCAGTGGGTCGA | 26259 |
rs181182827 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966637 | TGCTGCTGGTTTTAT[A/G]TTGTGAGAATTGTCT | 26259 |
rs181211223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936702 | CTCCGGAACTATAAG[C/T]GAATAAATCTGTATT | 26259 |
rs181223508 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920223 | TTCGTGAATTAGCAG[G/T]CCTCCACTTACGAAC | 26259 |
rs181236930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977721 | TGATGTCTCTTTCAC[A/G]TTACCTGCCCTCTGG | 26259 |
rs181237278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008297 | CTTTTATAATAGAAC[A/G]TGAGGTTGCTCTTTT | 26259 |
rs181262527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026868 | CGCAAACCTCTGTTC[A/G]AGAGACTTGGAACCA | 26259 |
rs181286792 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955994 | CCCAGGAGTATGATG[C/G]TGTTTTGCAATAAAC | 26259 |
rs181300530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012514 | GGTTTAAAATCTGTT[C/G]TTTTAATAAAAATTG | 26259 |
rs181307268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987397 | CACCGCGGAGAAATG[A/G]GCCGCCTGTGGATGG | 26259 |
rs181310193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941545 | AAACTTTAATGTGTC[A/G]TCAGTGTTAGGTTGG | 26259 |
rs181311513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993184 | TCTCGGCTCACTGCA[A/G]CATCCACTGAGCGGG | 26259 |
rs181312877 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971681 | TGAGAGCTGTGAGAT[A/C]TGTAGGAATTTTTTT | 26259 |
rs181316775 | snp | A/T | 0.0360663 | 0.129354 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923729 | ATTAATTTATTTATT[A/T]ATTTATTTTGAGACG | 26259 |
rs181361906 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023279 | CATCCTTGTGCTTGT[C/T]CTGTTCCTTGCTAGA | 26259 |
rs181398780 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984451 | TTGGCAAGTGTGGGA[C/T]ATTGAAGCACAGGTT | 26259 |
rs181468699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919555 | GCTATGCTATTTTAC[A/T]TCCTCTTTACTGAAG | 26259 |
rs181478895 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936228 | GGCAGAGTGGAATAG[A/C/T]AAGGACGAAGGACTT | 26259 |
rs181516218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003737 | AGCTTGACAGTTATT[G/T]TTGCTCAGCCTTTGA | 26259 |
rs181527326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959845 | CTCAACCTTGCCAAG[C/T]GTAGAAAAGACTGGG | 26259 |
rs181660301 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994848 | ACTTGGTCCACATGA[A/T]TGTATTTGTAGGATC | 26259 |
rs181668069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023073 | AAGAAAAAGAAGTCT[G/T]TCTTTATTATGCCTT | 26259 |
rs181668110 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973663 | GTCCTCTTCAGCACT[A/G]TCAAGGTCATGAAAC | 26259 |
rs181668325 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915469 | CAAGTGTACACATCC[A/G/T]TGTAAACAGCAGCCA | 26259 |
rs181671267 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003357 | TCCTTCCAGACAGTG[C/T]GGGGGGCGCACCCTG | 26259 |
rs181676562 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931998 | CATGTGGCCTTTATT[C/G]TGTTAAAGTACATTT | 26259 |
rs181676630 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951244 | TCTAAGAAAACCTTA[C/G/T]GTTGATGGCTTAGCA | 26259 |
rs181729668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959770 | CTTGAGAGAGGCTCT[A/G]TTCCCATTCTTTCAA | 26259 |
rs181744358 | snp | C/T | 0.00198023 | 0.0314037 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024112 | CTTTGACTCTAACCC[C/T]ATTTCCCTTCTCTGC | 26259 |
rs181770507 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031035 | GAGCATGCTGCCAGG[A/G]GAGCTGGATGGTGAA | 26259 |
rs181794330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923323 | ATGTGTAATACAGGA[C/T]GAAAGTCCCCAATAG | 26259 |
rs181881959 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983882 | ACAGTCCTATGTAGT[A/G]GGTAATGTTGTCTTC | 26259 |
rs181938768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941343 | CTCAGCATTAGAGTG[C/T]GACACTTAGATTCAG | 26259 |
rs181954386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013510 | GGGAGTGATGCACGT[A/C]GGCATTAGGGCTGGC | 26259 |
rs182009350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017305 | AGACCATCTAATGCC[A/G]GTCCAGAAAGGTTCA | 26259 |
rs182012307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930933 | CCACCTCAACCTCCC[A/G]AGTAGCTGGGACTAT | 26259 |
rs182024260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999738 | CCCATCTTAGCTCCT[A/G]GCTCTCTAGTCCTGT | 26259 |
rs182030657 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116976894 | TTTTCAAAATCATTT[C/T]AGGGGGTAATCAAAA | 26259 |
rs182035177 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954901 | TCCCTCCAGCTGGCT[C/T]CATCCCAGCCCCACT | 26259 |
rs182053192 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013624 | GTATATTAAAAAAAA[A/T]TTTTTCACATCTATG | 26259 |
rs182069686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972610 | GGCCTGGGAGCTTGG[C/T]GGCATACAGGGAGAC | 26259 |
rs182204362 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028467 | CAGGGATCTCGCTGC[A/G]CGGTCCTATACGGTC | 26259 |
rs182210001 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937402 | CTGGTGCTCCACAAG[A/G]ATTAGAGGCCGTGGA | 26259 |
rs182225054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989569 | AGGTTTTTAATGGAA[A/G]TTCTTTGAGTGATGA | 26259 |
rs182233901 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030464 | TCAAGCCCCGCCCTT[G/T]CTCTCTCATAGTCTT | 26259 |
rs182240355 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011001 | ATTTTCCCGGTATAG[C/G]GGCCTGTGCCAGCCC | 26259 |
rs182244386 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947044 | CTGTGTTTTTTGCTT[C/T]CTCTTTGGTGATAGA | 26259 |
rs182280053 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920720 | CCAGGACCCGCACTT[A/G]GTTTAATGCTCTGTT | 26259 |
rs182293222 | snp | A/G | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915027 | CCAACAACTCTCTCC[A/G]GTGGCTATTTTCAAC | 26259 |
rs182341698 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990722 | GACAGTTCAGCACAA[A/G]GATCCTTCAGATACA | 26259 |
rs182342806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027842 | GCGCCCATCGGACTT[A/G]TGCACCCCCACGTTG | 26259 |
rs182347792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969605 | TAAAATTTGTGACAC[A/G]GAAAAGAAGAATAAG | 26259 |
rs182357330 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994457 | GAAGGAAGGGTATGT[C/G]GTGGGAGGACTCCTT | 26259 |
rs182373216 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950875 | CGGATGCTACAGTTT[G/T]GTGTGAACTCCGGAA | 26259 |
rs182438085 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020334 | TGTTTCCCCATTTTT[A/T]AAATTATACTCTTAG | 26259 |
rs182488889 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008829 | GCTGAGGCCAGGCGT[G/T]CTGGCTCATGCCTGT | 26259 |
rs182505486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967829 | TGGAGTGCAGTGGTG[C/T]GATCTCGACTCACTA | 26259 |
rs182521084 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990162 | TGATATATTCTTCAT[A/C]CAGGAAGATAGACTA | 26259 |
rs182530213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968695 | CCATGAGAGTGTGCC[C/T]GCTTCCTCACAGTTT | 26259 |
rs182538371 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947645 | CTGGGAGGCTGAGAT[G/T]GGAGAATCGCCTGAA | 26259 |
rs182597364 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929095 | ACAGGCATGAGCCAC[C/T]GCGCCCGGCCCCATT | 26259 |
rs182618440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116911854 | TTTAATTTTTGTAAC[A/C]GTGCACGTATTCAAA | 26259 |
rs182624196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928792 | TCAGATTCAGGAAGT[C/T]TGCGGTGGGGCCTGA | 26259 |
rs182634056 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001216 | AGAGTGAGTAGAGGC[A/C/T]GTTATGCCTTAGGGA | 26259 |
rs182651207 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956549 | TGTAGACAGAGAGCA[A/C]AATTTGGAGCTTCAA | 26259 |
rs182764621 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943377 | TTGCTATTGTTATTT[C/T]TGTTGTTGCTGCTGT | 26259 |
rs182774033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116974316 | ACCTGAAAGGAGAAG[A/G]CACAACAATTCCTGG | 26259 |
rs182788757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981000 | TATTCACTGTGATAT[C/G]CCCAGTCCCTAGAAT | 26259 |
rs182796381 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010860 | AAACGATGTCAAGAG[A/T]GTATTTCAGAACACG | 26259 |
rs182802814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938529 | ATTTAAAATGATTTG[A/G]CATTTTCCTTGAAAC | 26259 |
rs182822374 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015090 | TGAGGACGGCAGGGG[C/T]CCCCTTTTGTTCCTC | 26259 |
rs182836375 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996906 | CCTTGTGGTCCTTAA[C/T]AGCGACTTGGCGATG | 26259 |
rs182838651 | snp | C/G | 0.0115144 | 0.0749975 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031505 | TATCACCTGAGGTCA[C/G]GAGCTCAAGACCAGC | 26259 |
rs182843019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014173 | CCGTTGCTCTGACTT[C/T]AGGTTTATGGACTCT | 26259 |
rs182843209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924339 | CATATTTATGGGGCA[C/T]GGTGTCATATATGTA | 26259 |
rs182844437 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024953 | GCACAGGCTGATGGC[A/C/G]TCACAGAGGTAGGTA | 26259 |
rs182846153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963552 | GAGGTTGCAGTGAGC[C/T]GAAATTGTGCCACTG | 26259 |
rs182848092 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995253 | TTATCTGGGACCCAT[C/T]TGAGGAAGAGCCCAC | 26259 |
rs182863139 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912542 | TCGGCTCACTGCAAG[C/T]TCCGCCTCCTAGGTT | 26259 |
rs182908250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018600 | TCTGCTGTTTCTGTC[C/G]ACGAGAAGCCAGAGT | 26259 |
rs182919240 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948000 | TGTGCTGTGCGTGCT[C/G]GACTTCAGGATGGGT | 26259 |
rs182924282 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978864 | TTCAGGCAATTAACA[C/T]AATTACCATTATGCT | 26259 |
rs183072756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002496 | GATTTGCATCTTGCC[A/G]GTTGCTGCTGCGAAG | 26259 |
rs183086912 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957781 | CGATCATTACCCGTT[A/G]GGGACCTCTTTTTAA | 26259 |
rs183093878 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005150 | CTGTTTTGGGTAGGA[G/T]GGAGCAGTTCCTTTG | 26259 |
rs183097307 | snp | A/G | 6.67e-05 | 0.00577456 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985396 | GGAATTTGAAGTTCC[A/G]AAACTGGTGAGCTTT | 26259 |
rs183121839 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116952557 | AGCGTCCATTCTTCT[C/T]GGAACTCCTAGAGAC | 26259 |
rs183177151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923822 | GCCTCCCAAGTTCAC[A/G]CCGTTCTTCTACTTA | 26259 |
rs183179950 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025354 | AACCGAGATGATTCT[A/G]GGCCAGTGGCCTCTG | 26259 |
rs183188608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917194 | AAAAGCTCTTCCAAT[G/T]TTTAATTGTTGGTAA | 26259 |
rs183194267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116916332 | GATAGTAACTTGTGT[A/G]TGTGGAATGTAGTAT | 26259 |
rs183200925 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942715 | AAACTTGTTGTTGAG[C/T]GCCTTTAGGGAATTT | 26259 |
rs183214073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986169 | GGCCTGACCTGGAAC[C/T]AATCCTGTTCCTCCC | 26259 |
rs183341008 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032434 | ACAGTGGCCCCAGCC[A/G]GGAATCAATTTTTTT | 26259 |
rs183376918 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957298 | GTTGCAGTGAGCCAG[C/G]ATCATGCCACTGCAC | 26259 |
rs183435070 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006039 | GCTTTTAAAATGCTA[C/T]TGTCTTGTAAGGAAG | 26259 |
rs183437133 | snp | A/G/T | 0.00438556 | 0.0466571 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019824 | CCGCCTTTATTGCCC[A/G/T]CTTTCTTCTCCAAGG | 26259 |
rs183438367 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921554 | TTACCTCTATAAAAG[A/T]TTTTAGCTCTTTGAG | 26259 |
rs183440802 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923955 | CCTGACCTCGTGATC[C/T]GCCTGCCTCGGCCTC | 26259 |
rs183441564 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001758 | TCCCAGTCAGTCATA[C/T]ATTTGCACGATGGTT | 26259 |
rs183444564 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938025 | TTTGGAAAATTCAGG[A/C]TTGTAAACTTGCTAG | 26259 |
rs183451086 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980625 | AATTTATATCAGATT[A/T]AAAAAAAAATACCTA | 26259 |
rs183485637 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005463 | AAACCTAGGAGAGTG[G/T]TACAACGTGTAGTGT | 26259 |
rs183514986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961994 | GCAGAACAGAACAAG[A/C]TTGGCACCTGAGCAT | 26259 |
rs183544954 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012854 | TAAAGGTACATAAAA[C/G]TGCCCCAGATTAAGA | 26259 |
rs183621613 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030136 | AGCCTAGAACCTTCA[C/T]GTCATGAAGGTTCTG | 26259 |
rs183645598 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014788 | AGCCGTTGCCGTCCT[A/G]CTTTGAATCTGTCCC | 26259 |
rs183662312 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116974843 | GGAACAAGGGCTAGG[A/G]CAGATAAATACAAGA | 26259 |
rs183696544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933654 | GAAAATATTCTTAAA[C/G]AGAACCCCGTTAGCG | 26259 |
rs183730814 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958819 | CTCCCCAACCAGTAG[A/T]GATCATGAATAACTC | 26259 |
rs183738853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985881 | TTAAAGTAACTCTTG[C/T]GTGAAGATAGATTTA | 26259 |
rs183752580 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943227 | GTTAGCTTCTGTTGA[C/T]TGCCTTTTCCCCTGT | 26259 |
rs183809803 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949842 | GCCCATGTGGAAGAG[G/T]GAGAGTCTCCGTGAT | 26259 |
rs183830307 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922398 | TCAGTCATAGATTTA[A/G]TAAAAATGTTATTGC | 26259 |
rs183842657 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939484 | AGCGTGGAATCCTTT[G/T]CTAAGGAACTTATTA | 26259 |
rs183864193 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031988 | AGCGATGGTGAGTTA[C/T]ATCACAGAATAAATG | 26259 |
rs183864615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913537 | CATTAAGAAAATTAT[A/G]AGAGAAAATGTATTT | 26259 |
rs183875320 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929577 | TTTATTTTTTTAAAT[G/T]GACAAATAAAGTTAT | 26259 |
rs183878565 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012182 | CTGCCTCATTATGTA[C/T]GCACTGCCAGGGAGG | 26259 |
rs183879758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992226 | AGTCACCTCCAGCTC[A/G]GGTAGGAAGGGATCA | 26259 |
rs183889460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971418 | TTTAAGAAATCCTTT[C/T]TAGGGCGTTGAACTT | 26259 |
rs183894926 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953074 | TGAGTGGTATGTAAT[A/G]TTTTGTTAAATGTAT | 26259 |
rs184023759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988548 | GTGAGTGTTTCATTT[A/G]CCCATCTTTTTCTGT | 26259 |
rs184053372 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910473 | TGTATATATCAGTTT[A/C]TTTATCCACCTGTTG | 26259 |
rs184123490 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967153 | GCTCTGTATACTTCT[C/T]TGCACCTTTTTTTTT | 26259 |
rs184126743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016563 | ATTTTCTCCCATTCT[G/T]TGGGTTGTCTTTTCG | 26259 |
rs184131229 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997965 | GGACTACAGGCGTGT[A/G]CCACCATGCCTAGCT | 26259 |
rs184210867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928491 | GGTTAAATCGAGCCT[G/T]TTATTAGGTTGGTAG | 26259 |
rs184240898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972181 | CACAGTAGCTGTTCT[A/G]TTTTATTACAGTTGA | 26259 |
rs184252937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002562 | AAGTCACCTTTGGGA[A/T]GGTGGTGAAAGTCAT | 26259 |
rs184290228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975185 | ACCGTAATCATAATT[G/T]TCGTAGGCAAGAATC | 26259 |
rs184312964 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930394 | TTCTCTGATGATTAG[A/T]ATTGTTGAGCATTTT | 26259 |
rs184361176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917745 | TGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 26259 |
rs184367971 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116934133 | TCCCACAAACCATGC[C/T]GGAGACTGATTTTGC | 26259 |
rs184376446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021803 | TGGTTTTTAAAAAGC[A/G]ATGTGAAGTAATGGT | 26259 |
rs184384706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953269 | CTTTAGAGATGATGC[A/G]TTCCAAGACCCTCAT | 26259 |
rs184398211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950445 | AGCTATGGAGTGAGA[C/T]GCCTTAGGGAACTTC | 26259 |
rs184406014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981863 | AAGTGATACGCCCAC[C/T]GCAGCCTCCCAAAGT | 26259 |
rs184428547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914494 | GGGAGGATTGATTGA[A/G]GCCAGGAGGTCGAGG | 26259 |
rs184607645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023123 | AGGTATAGAATTGTT[A/G]GTTCAAAATAATTTT | 26259 |
rs184727668 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986612 | GCCTGGGCAACAGAG[C/G]GAGACTCCGTCTCAA | 26259 |
rs184733322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964412 | GCAGATTGTTGTAAT[A/T]GTGTAAAAGGAAAAG | 26259 |
rs184739449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944586 | TGCAGACCGGGATCA[C/T]GCTGATCTGCTCGAT | 26259 |
rs184742055 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922045 | ATGTTACCTGGGCTG[G/T]TCTTGAACTCCTGGC | 26259 |
rs184750987 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029610 | TATAAAGCCAGAAGG[G/T]TTTGTTTTTTTTCAG | 26259 |
rs184792061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025570 | CATGCAGAATGGGCT[G/T]CTTCCTTGGAGGGCA | 26259 |
rs184793457 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116918799 | AAATAGAGGAAGTGG[A/G/T]TGTTGGGCAGGAAAA | 26259 |
rs184795693 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927838 | GAGAATGGAGGATGG[C/T]TGGCAGATTCTGAAA | 26259 |
rs184798259 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027011 | CCAGTGCTCCATAGA[A/T]GATGGAGAGCCTGGC | 26259 |
rs184805653 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935866 | GTGTCTATGACCTTT[A/G]AGAATTAAAAGCAAT | 26259 |
rs184809016 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006544 | TGCCTCCCAGTTGTT[A/G]GGCCTGTAGCTGGTG | 26259 |
rs184876714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912675 | TCACTGTGTTAGCCA[A/G]GATGGTCTCGATCTC | 26259 |
rs184880927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918342 | CATTTTTATTTAGGT[A/G]GTGTATCAGGACTCT | 26259 |
rs184916963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008357 | ATAATTTTTAGGTTA[G/T]TCTCTGATGATAAGA | 26259 |
rs184950052 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953975 | AAAAATTAGCTGGGC[A/G]TGGTGGCGGGCACCT | 26259 |
rs184957394 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022997 | TTGTTCTGGTATTTT[C/G]CTATGCCACTTTCTT | 26259 |
rs184961203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003329 | CTGCACAGGTATCCA[A/G]AGGAGCTTCTGTTCC | 26259 |
rs184987741 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959936 | TCAGTTTTTCCTTAG[A/T]GTTCTTACATCAGCT | 26259 |
rs184996263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941826 | CTCTGTTTTTTGAGT[C/T]ATTTTCTTAGTTGTT | 26259 |
rs184999130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935774 | AAAAAGTTTACTAGA[A/G]AAAAAAGCATAAAGC | 26259 |
rs185050099 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975774 | ATTGAGAGGCCTACA[C/T]AATAAATGAGCAGTA | 26259 |
rs185055888 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923759 | GGAGTCTTGCTCTGT[C/T]GCCCGGGCTGGAGTG | 26259 |
rs185066806 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983076 | TGGAAGTGAATGCCC[A/G]GTGAGAGGAGACACA | 26259 |
rs185073564 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985119 | TATCTCCGTTAAAAA[A/T]TTTTCCTTTGTGTTG | 26259 |
rs185077390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959126 | TGAGAAGCAGGCATG[G/T]GAGGCAACAGGTTGC | 26259 |
rs185085345 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940269 | TCTTTTTTTTTTTTT[A/T]AATAATTAAGACACA | 26259 |
rs185087108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007645 | TATCTGTACACCTCT[A/G]AGAATGAGTCAAGTG | 26259 |
rs185102475 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966082 | AAATATTTTTATATT[A/T]TATATAATTACTTTA | 26259 |
rs185120198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927317 | AGGCGAGCTCTGATT[C/T]CTCTGCATTAATAAA | 26259 |
rs185184789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026674 | TTCTTTGTAGCTTGT[A/G]ACATCGCTCGTGCTA | 26259 |
rs185204531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986841 | AATCTGAGCCTCTTG[A/G]TCTGTCAGAAAGCCA | 26259 |
rs185216527 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027705 | ACAGCCCCGTGGGGC[A/G]AGTCCACGCTGTCGG | 26259 |
rs185225489 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945174 | GGTGGTACAACAATT[C/T]TGAAATCTTGAAAGA | 26259 |
rs185275805 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031726 | CTCAAAAAAAGAAAT[A/G]GCAACTTTAAGCAAA | 26259 |
rs185431739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017011 | TGTGTTCTGGCACTA[C/T]CACGCTGTACAGCTT | 26259 |
rs185446268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976538 | TCAGCTCGCTGCAAC[C/T]TCCACCTCCCAGGTT | 26259 |
rs185522594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915853 | AGATGGGGTTTCACT[A/G]TGTTGGCCAGGCTGG | 26259 |
rs185529057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932000 | TGTGGCCTTTATTGT[A/G]TTAAAGTACATTTCT | 26259 |
rs185558283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925807 | TTTTATTCTTAATAG[C/T]ATACCTATTTCATAG | 26259 |
rs185559767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994912 | ACATGTGCCTCCATG[A/G]TTTTGATAGACATTG | 26259 |
rs185562345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999527 | AAAATAATCCCTCCC[C/T]GAGCGCATTTCCCCT | 26259 |
rs185568632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973753 | TGCAGTGTGTCATCC[C/T]GGCTTGGGTTGTTTT | 26259 |
rs185576384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951532 | TATTCTTCTTTTTTC[C/G]TTCCCTTTTCTCTTT | 26259 |
rs185582262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954776 | TCAGCTTCTTTGCAA[A/T]CTAACCTTTTGACTT | 26259 |
rs185590489 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909058 | ATGAGCCTAAATTGC[C/T]ACAGTAGGACCAACT | 26259 |
rs185602519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927370 | TGTTTGCACTGGCCC[C/G]CTCAGGTTAACCAGT | 26259 |
rs185629665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945678 | TTGGTGACTTGTTGC[A/C]CATTTTGTTCACCAT | 26259 |
rs185670083 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922814 | TGTGTGTGTGTGTGT[G/T]TTTTTTCCCTTGACT | 26259 |
rs185711170 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017927 | TTGCCCTGACAAATA[G/T]AAAGTTGTGTGCTGT | 26259 |
rs185714182 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029212 | GCACAAAGATTCACA[C/G]CATACAGGCCAAATT | 26259 |
rs185726808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991310 | AGAGACAAGACTTTC[C/T]ATCTGATTGTGCTTA | 26259 |
rs185742846 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948609 | CTTACACTGTTTCTA[A/G]TCTTTGTCCCAGTCT | 26259 |
rs185788571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929193 | TATGCCATTAACATC[A/G]TTCTCTTGTTCTCGT | 26259 |
rs185844614 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011862 | GCATAATTTCAAAAA[C/T]ATTAAGAAAAAAATT | 26259 |
rs185867597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970211 | CTCGCTCTTTGGTGA[C/G]AAATGAGATTACACA | 26259 |
rs185938592 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004320 | GTATTCTTTATTTGA[A/T]CTTGCCTGGAAGTCT | 26259 |
rs186004415 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977001 | TGGGCACAGGGGAGG[C/G]AGACCCGAGAGCCCC | 26259 |
rs186012777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955145 | AGGAAAACTCCCCTT[C/T]GGCGATTCCACACTC | 26259 |
rs186061635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919819 | GTTTTAGGTCTGCTG[A/G]AAGTTTTAATACTGC | 26259 |
rs186061928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023340 | TGTCTTTTCCTTTTC[C/G]ACTTGCATCACAGGG | 26259 |
rs186069500 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936333 | TGGGTGGTTGTCGTA[C/T]GCTGAATAATGGCCC | 26259 |
rs186077934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019054 | ACAGCATTTATACTT[C/T]TTCTCTTCTCTTACC | 26259 |
rs186078257 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910479 | TATCAGTTTCTTTAT[C/T]CACCTGTTGATTCTC | 26259 |
rs186086311 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017330 | GGTTCAGTGACCAGT[C/T]AGTCCGAAGGGCTTG | 26259 |
rs186095024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937562 | CGCTGTTGTTCATCA[A/G]GTAAGAGGAGGACTG | 26259 |
rs186102038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979646 | CTACTCAGAATTAAT[C/T]ATCTTTTATCCAGCT | 26259 |
rs186109637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008708 | GTAAAAATCTGTATC[A/G]TGGTAAGTGATAAAT | 26259 |
rs186117582 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957172 | GCCAACATGGCAAAA[C/T]CCCTTCTCTACCAAA | 26259 |
rs186127596 | snp | A/G | 0.00138127 | 0.0262436 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988890 | CAACTAGCAAGATAT[A/G]TAATTAACAAAAAAG | 26259 |
rs186133425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967755 | TCCGATATTTTTTCC[A/G]TAAGTCACTTATTCT | 26259 |
rs186218647 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031048 | GGGGAGCTGGATGGT[A/G]AAACACCTGAAGATC | 26259 |
rs186227702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014098 | TTTCCAACAGGCCAC[C/T]AAAGCTCTGTTCATG | 26259 |
rs186227975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001235 | ATGCCTTAGGGAGCT[A/G]GGGGGAGCCCCTGGG | 26259 |
rs186230826 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983984 | GGAGCTGGATTTGAA[C/T]TCAAATAGTCACAAA | 26259 |
rs186245431 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941368 | ATTCAGAAAAATGAC[A/G]GCTTTGTCACTTATT | 26259 |
rs186266578 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005300 | AATCAGTGAGCCTCC[A/G]AACACAAATGCAGGC | 26259 |
rs186274334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985528 | GCCTTACCTCCATAA[A/G]TCTAACTACAGCCTT | 26259 |
rs186277002 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961872 | AAGGGCTTGGCTTGT[A/G]GGGGGAGGATTGAAT | 26259 |
rs186364302 | snp | A/G | 9.89234e-05 | 0.0070322 | missense, synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024167 | GGATCCACGACCTCC[A/G]CAGTGGTAACATCGC | 26259 |
rs186366060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003368 | AGTGCGGGGGGCGCA[C/T]CCTGGGCATCTGGCA | 26259 |
rs186371104 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000564 | ATTTGCATGTCTAAC[A/T]AGTGCCCAGAGCAGC | 26259 |
rs186380438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956377 | AGGCAAGTGTGCCCA[A/G]GTAGATACAAAACAA | 26259 |
rs186413434 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923551 | TTGAGACAGAGTCTC[G/T]CTCGCTCTGTCACCC | 26259 |
rs186501075 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920361 | AATATTTATTAAGTG[G/T]CTTCTTGGTACCAGC | 26259 |
rs186537146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915186 | CCCAGAGCCCACAGG[A/G]CTAAGGCAGGTAATG | 26259 |
rs186548948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931013 | GGGTCTTGCTTTGTT[A/C]CCCAGGCTAGTCTCG | 26259 |
rs186580499 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978080 | TCTAAAATGCAGATT[C/T]CAGAATGTTTTCTGT | 26259 |
rs186613674 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936990 | GGACAGCAGCAAGGA[C/G]ACCAGTTAGGAGGCC | 26259 |
rs186638943 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117006060 | TGTAAGGAAGCCTTC[C/T]GACTCCTCCTGGGCT | 26259 |
rs186708607 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925042 | GGAATATATTGAACA[C/G]AGGACTATCGTGGGT | 26259 |
rs186725050 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969731 | TCGGTGGAGGGAATC[A/G]TATCCAGAGGGGGAG | 26259 |
rs186736464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009286 | TGGCCCCAGCTACTC[A/G]GGAGGCTGAGTGGGA | 26259 |
rs186747501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928522 | CTGAGGGGGTCAGCA[C/T]GAGGACAGAACATGT | 26259 |
rs186749554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968153 | AATCTAAAAGTGAGT[A/G]GGGTTATTTTGTAAT | 26259 |
rs186754623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986313 | CTGATGCTGTCAGCT[C/T]ATCTGGGTTTTATTA | 26259 |
rs186759176 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963900 | AGTGGAGTAAAACCC[C/T]CTGCAGCAGACATAA | 26259 |
rs186767285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944072 | GTTTTTACAGCTGCT[A/G]TCTTCACGAGGTTGT | 26259 |
rs186868315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947471 | CATGAAAGGCGGCCC[A/G]GCACCGTGGGTCACT | 26259 |
rs186891107 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028469 | GGGATCTCGCTGCGC[A/G]GTCCTATACGGTCCC | 26259 |
rs186907025 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011514 | AACTCCTCAGTGTGT[C/G]TGTGGGGCACGCACT | 26259 |
rs186910425 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990997 | TCTACCACACACACA[A/C]AAAAAAAGTATAGTC | 26259 |
rs186939515 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027928 | GTGAAGCTGAACCTC[C/T]ATCTGGTCTCAGGCG | 26259 |
rs186954849 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989958 | GCACATGAGAGCTCC[C/T]GACCTGTTAGCTCCT | 26259 |
rs186984583 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909528 | TAGCTACTCAGGAGG[C/T]TGAGGCAGGAGAATG | 26259 |
rs187066798 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946769 | TGCCCGTGTGCCTGG[G/T]TAGGTCCATGTGATG | 26259 |
rs187177026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990205 | TATGTGTGGCATCCT[A/G]TCATCTCAATGTGAA | 26259 |
rs187187478 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969198 | ATAAGTGCTTCCAAG[G/T]CTGCAGTGTTTCCAT | 26259 |
rs187192835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947799 | TTGGGGCAAGTTGCT[G/T]TACTTTTGTCTGCCT | 26259 |
rs187197794 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030569 | TTTGCAGGCGCATTC[A/G]CCCTTCCTAGTTTGC | 26259 |
rs187199390 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928118 | GAAAGAACTAGGAAG[A/G]TGTGCACAGGTAAGG | 26259 |
rs187213248 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994707 | ATAACAAAGAACTTT[C/T]TCATGTTTTGGTTTT | 26259 |
rs187231151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950984 | GACTGAAAGAGTCGC[A/G]AAAGAACTTAAAAAT | 26259 |
rs187231990 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912300 | TCAAGCCATCCTCTT[A/C]CCTCAGCATCCCGCG | 26259 |
rs187236942 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923865 | AACTGGGACTACAGG[C/T]GCCTGCCACCAGGCC | 26259 |
rs187239495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928795 | GATTCAGGAAGTCTG[C/T]GGTGGGGCCTGACAG | 26259 |
rs187246129 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028339 | TGCACTTCCCCCAGC[A/G]CCTGGGGCAAGCTGG | 26259 |
rs187261124 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010985 | TGGCTTAGGGAGTCG[G/T]ATTTTCCCGGTATAG | 26259 |
rs187296011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938435 | CGGGGTTAGTGATGT[A/G]AATGATGCACCACAA | 26259 |
rs187306852 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929234 | AAGAGTGTGTGATTG[A/G]TTTTTCTTTTCTTTT | 26259 |
rs187326959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019864 | TTAATGTTTCAAGTA[C/T]GTGCTTCCAGAATTT | 26259 |
rs187334211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001868 | ATCACATTTCTTACC[C/G]TTACACCAGCACTGA | 26259 |
rs187340858 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980700 | CTTCCTTAGTAGTTA[C/T]GCAATAAATGCAGAC | 26259 |
rs187349483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957512 | ACTCGCTTAGTTTTA[C/T]ATGTATGTGTGAAAA | 26259 |
rs187414089 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013511 | GGAGTGATGCACGTC[A/G]GCATTAGGGCTGGCT | 26259 |
rs187425398 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942800 | TTTTTTTTTTTGAGA[C/T]GGGGTCTCACTCTGT | 26259 |
rs187429831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972780 | GGTGTTAAATATAGA[C/T]AGAGAAGTAAACAGA | 26259 |
rs187464595 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015726 | ATTCACCAATTTAAA[C/T]TGTACAATTCAGTGT | 26259 |
rs187472188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997429 | CTGGAGACTGAGCAA[A/G]GGTTCTGCAGTCAGG | 26259 |
rs187479229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975242 | TGAATGTCTCTGTCC[A/G]TTTGGGCTGTTATAA | 26259 |
rs187483411 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953383 | GCAGGGCTGGCTGGT[G/T]AGGCTGCCGTTTCCA | 26259 |
rs187511698 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934401 | GACAGTTCATTGAAC[A/T]GGTTTGTAATCTTGC | 26259 |
rs187521713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932931 | TATTGTTGTTAGTAT[C/T]GCTTAAGTGGGGGCA | 26259 |
rs187558137 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921188 | AAAAAAAGGATAAAT[A/C]AAATTCCATGGACAT | 26259 |
rs187579823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116974775 | TGTGTACCCTGGTAA[C/T]AGTAAGCACAGCTAG | 26259 |
rs187718010 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116948383 | CAGCTCCACGTGGAT[A/G]TGTCTAGTTTTATCT | 26259 |
rs187721768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025403 | AGCAGAAACAGGGCA[A/G]GGCCCTCCCACAGGA | 26259 |
rs187763238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953147 | TCCCCTTGTCCCCTG[C/T]CACCTATATATGATG | 26259 |
rs187830307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917290 | AGATCTGCCTTGGGT[A/C]ACCATTTTATCATCT | 26259 |
rs187836545 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933774 | GAATTGGCTTTGTTT[A/C]ATCAATCATTAAAAT | 26259 |
rs187837042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943327 | ATGGAAACTCTGGAA[A/G]TAGAATCTTTCTCCC | 26259 |
rs187841777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995882 | CCTTTAAAATCTGCT[G/T]TTATGTCTCATAGTT | 26259 |
rs187857425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952617 | ATCGTGTGGCCTTGC[C/T]GTTTCACTGAAACAT | 26259 |
rs187857771 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916954 | ATCTGGGTTATGAGT[C/T]ATCATACAGCAGCTT | 26259 |
rs187958188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007258 | ATACTTTAAGATCTC[C/T]AAGAAAAAAAAAAAC | 26259 |
rs187962032 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008432 | CTTGATATTTTAAAA[C/T]TGTTGAAATGTTCTG | 26259 |
rs187966097 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988553 | TGTTTCATTTGCCCA[C/T]CTTTTTCTGTTGGGT | 26259 |
rs187973030 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986661 | AAACAACAAAAAAAC[A/G]AATACTGTAGACCAG | 26259 |
rs187977835 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967593 | TTTCTTTAATTACAT[A/G]TGGACATCTTTTCTT | 26259 |
rs187982941 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017946 | GTTGTGTGCTGTGCT[C/G]GTGCTACTGCTGCCT | 26259 |
rs187985680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945948 | GATGATTAAACATCT[C/G]TAAGCACTGTCTTCT | 26259 |
rs187997658 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969805 | TTAGCCTCTTTGCTC[C/T]GTAGGAACACTGTAC | 26259 |
rs188009556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927588 | TTCCTAGTTGAGAGT[A/G]GTGGTGGTTGTCCTG | 26259 |
rs188031398 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930060 | GTATTCCATTGTGTA[C/T]ACATGCCACATTATG | 26259 |
rs188048498 | snp | A/G | 0.000247723 | 0.0111266 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027460 | CGTGCCTTACCAGAC[A/G]GTAATGCGAAACGCC | 26259 |
rs188057842 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002535 | AAAGGCAAGCTTCTG[A/T]TTGCCAACAGAAAGT | 26259 |
rs188066340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922157 | TTTTTCTTTTTGTAT[A/G]TAAGAATATATATTT | 26259 |
rs188077679 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958149 | ATTATTTTTCAATTG[A/G]TGCGTCTTAAGCCCC | 26259 |
rs188102107 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924010 | GAGCCACTGCACCCG[A/G]CCCAAAATTACTTTC | 26259 |
rs188103906 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909165 | GAATATACGCCCAAC[C/T]ATATACTCTAATTTT | 26259 |
rs188208773 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011925 | GCAGCAAGCCAAGTA[A/C]TATGTTGAATCATAA | 26259 |
rs188270219 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939225 | CTCCAAAATTAGAAA[C/T]TTTTTCAGTGCTCAT | 26259 |
rs188323992 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030266 | CTTCCCGTCCAGAGC[A/G]CTTTCTTTCAGACCC | 26259 |
rs188329612 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970359 | GGTGCCATCAAGCAC[A/G]GCAAAGTGGCTTATC | 26259 |
rs188334899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020777 | CTGAAGTCGCAGCTC[A/G]CCCTCTCCTGTCTGG | 26259 |
rs188351217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981152 | ATTCAGTTATTCACT[A/G]TTCAAGTCCTTGCAG | 26259 |
rs188389032 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982389 | AGTAACCAGGGATAC[C/T]GAGGGACTTTGCCTG | 26259 |
rs188401051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958901 | CTTCTCAACACAGAG[C/T]TCTAGGCAACCACTA | 26259 |
rs188407516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939578 | TTATATGATCTCTTG[A/G]TTACTCTTGAGTCTT | 26259 |
rs188445076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922457 | TTCTCAGTTTCTTAA[A/G]CCACCACCCAGAGAG | 26259 |
rs188476241 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002801 | TGTCACTGGCTCCCC[C/T]TCTCCCCAGTTGTCT | 26259 |
rs188488046 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029700 | CTGCAACCTCTGCCT[C/T]CCGAGTTCAAGCAAT | 26259 |
rs188489597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024976 | GGTAGGTAGGTTTAC[A/G]CCAGTGGCACCTAAC | 26259 |
rs188495387 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029223 | CACACCATACAGGCC[A/G]AATTATAGAATCCCC | 26259 |
rs188509550 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991928 | ATGTTACAGGCACCT[C/G]AGCTGCATGAGCATG | 26259 |
rs188509907 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985968 | CCTTAAGAATTCTTT[A/T]TGTCGAGCTTATTTC | 26259 |
rs188526687 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918013 | AAAAAAACAAAAAAA[A/C]AACAACGCAGGACTC | 26259 |
rs188547538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913572 | TTCATTAAGTGAAAG[C/T]GGCTCATCACAAAGG | 26259 |
rs188555374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929864 | CCAGCCACTGGTAAC[C/T]GCCATTCTACTCTCT | 26259 |
rs188566926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921626 | CCCCTAGCACCTGGT[A/G]TGGCCCTGAATTTAG | 26259 |
rs188595422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012226 | GTGTCAAAGGGCTCT[C/G]TGGTCAGTTTGCAGT | 26259 |
rs188618145 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971506 | ACAGAGACTGTATTA[A/G]GGGCTGGAGGAAGTT | 26259 |
rs188620369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912598 | CCCAGTAGCTGGGAC[C/T]AACAGGCGCCCACCA | 26259 |
rs188622942 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949259 | TTTTTCACATACTTT[A/G/T]TAAGTTTCTTTAGAT | 26259 |
rs188626259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950121 | AGAAGGGCTTTGGCC[A/G]CACATAATCTTCCTT | 26259 |
rs188789015 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005735 | GGCAGCTGGAGTGGA[C/T]GGAAAAGAAGAGAGC | 26259 |
rs188805221 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962324 | TTCTGTTTCACAGCT[C/T]ACTATTGTCTGGTTC | 26259 |
rs188844224 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032067 | AAACACCAGAATGAA[C/T]GGGCTCACTGGGCAC | 26259 |
rs188858848 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912810 | AAGAAATAATGGCCT[A/G]TTATTTTATGTAATA | 26259 |
rs188865559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996527 | CAAAAAAAAAACTTG[A/G]TATTTTACAAGCAGG | 26259 |
rs188881934 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022998 | TGTTCTGGTATTTTG[C/T]TATGCCACTTTCTTT | 26259 |
rs188895505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003346 | GGAGCTTCTGTTCCT[C/T]CCAGACAGTGCGGGG | 26259 |
rs188903667 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983720 | ATAGGGCTAGATTTA[C/T]GGATGATCAATAGAA | 26259 |
rs188905882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929135 | CTTTCTAAGCAGGGG[A/T]TGCCAGTGTGGCTTT | 26259 |
rs188911908 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959547 | ATTTTGTTTTTAGCA[A/C]ATAAGAGCTGACACC | 26259 |
rs188993520 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016745 | CCTAAGTTTTCTTCA[A/G]AGGGTTTTATAGTTT | 26259 |
rs189017091 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975811 | AAAAGTGTCAGGGTC[A/G]TGAAGGACAAGGAAT | 26259 |
rs189058128 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116974997 | ACTTGAGCAACAAAA[C/T]ATGATGATAGTGATG | 26259 |
rs189111432 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927318 | GGCGAGCTCTGATTT[A/C]TCTGCATTAATAAAT | 26259 |
rs189115039 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935826 | AAGGAGCCTACGGAG[A/G]GCAGCACATGCCAGG | 26259 |
rs189140737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014806 | TTGAATCTGTCCCAC[A/G]TAGCCCAGGGATGAG | 26259 |
rs189237263 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017494 | TTTTTTCTAGTTGCC[A/G]TTTAAAATGAATCTT | 26259 |
rs189239411 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000388 | TACTTACCACTGTCA[C/T]GGCTGAAGTTCTTCG | 26259 |
rs189260028 | snp | A/G/T | 0.00993419 | 0.0697739 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955181 | ACTTCCATTACCTCC[A/G/T]TGAGCGCCTTCTCTG | 26259 |
rs189274277 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950620 | ATATTTTGTGGCATG[C/G]AGTGCCTATGAAAAA | 26259 |
rs189292137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998049 | GTCTTGAACTCCTGA[C/T]TTCAGGTGATCCGCC | 26259 |
rs189351790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914993 | TAAGGGTTTAGAGAC[A/G]TTATCGTCTTCATTT | 26259 |
rs189356241 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993943 | TTTTATTTTTCTACA[C/T]GTGGTTATCCAATTT | 26259 |
rs189363348 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022003 | TTCTTTGATCATGCT[C/T]TCAGGGTTAGGCTTT | 26259 |
rs189387484 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, stop-gained, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116918595 | ATCTGCTTAGCAACT[C/G]AAGGGAAAGAGAGCT | 26259 |
rs189480533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116918903 | TATCCACTGGAGATA[A/C]ATTTCAAGACCCCCG | 26259 |
rs189488406 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935934 | CTCATTTGGTTATTT[A/C]TATAGAGCTGACTAT | 26259 |
rs189512752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003429 | TCATGGCATTTGACT[G/T]GTTGGAATAAAGACT | 26259 |
rs189526223 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116976779 | TTTAAAATGTCAACA[C/T]TTACAAACATGCCAG | 26259 |
rs189596250 | snp | A/T | 0.0737376 | 0.17729 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923725 | ATTAATTAATTTATT[A/T]ATTTATTTATTTTGA | 26259 |
rs189637067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013174 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 26259 |
rs189641321 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959825 | CCTATTTATTTAGAG[A/G]TAAACTCAACCTTGC | 26259 |
rs189646388 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930608 | GTTGTCTCTGTATTC[A/T]GTTGATTGTTTCCTT | 26259 |
rs189648464 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972461 | TTTGTGGAATGAATA[C/T]ATTTTTGTTTGAAAA | 26259 |
rs189705144 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028448 | CAGCTCCCTCAGGAC[A/G]CCTCAGGGATCTCGC | 26259 |
rs189715344 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010994 | GAGTCGGATTTTCCC[A/G]GTATAGGGGCCTGTG | 26259 |
rs189729580 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990481 | CATTTGTTGAGAGAG[C/G]GGAGACCATTTTGCT | 26259 |
rs189734806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969421 | TTCAGTTTAACAGAT[C/T]GACACTATGATATTT | 26259 |
rs189744837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929084 | GTGCTGGGATTACAG[A/G]CATGAGCCACCGCGC | 26259 |
rs189783420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023246 | AGCTTTTGGGTCAGA[C/T]GTGCGTTTTTAATCT | 26259 |
rs189793813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983988 | CTGGATTTGAACTCA[A/G]ATAGTCACAAACTGT | 26259 |
rs189815171 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923819 | TCCGCCTCCCAAGTT[A/C]ACGCCGTTCTTCTAC | 26259 |
rs189837280 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940506 | GGCTTTTTTTTTTTT[C/T]CCTTCCAGTTTGTGT | 26259 |
rs189868091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024043 | GCTGAGGAGTTTTTC[A/T]TAGCAGTGTTGTGCA | 26259 |
rs189870209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005068 | CAGAGGTGGGACTGT[C/T]GGACTGGATGTAGTT | 26259 |
rs189883543 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985140 | CTTTGTGTTGCATGT[A/T]TTTAAAATAATTGAA | 26259 |
rs189887826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961584 | GTAAGACTTTATAGA[C/G]GGTTCTCTGGGTATA | 26259 |
rs189898471 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116942437 | TGGAGTGCAATGGCG[C/T]GATCTTGGCTCACTG | 26259 |
rs189912079 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941380 | GACAGCTTTGTCACT[C/T]ATTTATGCCACGTGA | 26259 |
rs190102290 | snp | A/G | 0 | 0 | synonymous-codon, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945405 | AGAGGATGAGGTGCT[A/G]TGGTACAGGCTGTGC | 26259 |
rs190123573 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030995 | ACGCCTCCATCCCCG[C/G]CTCCCCTAAAGGTAG | 26259 |
rs190147441 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031485 | TTGGGAGACCGAGGC[A/G]GGCGTATCACCTGAG | 26259 |
rs190160306 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014137 | CAAACCTTTCTTTCT[A/G]TTCTTCAGGCTGCAT | 26259 |
rs190168187 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995157 | CTAGAATCAGTGTAG[C/T]ATGACTGACAGCCCT | 26259 |
rs190178358 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FBXW8 | GRCh38.p7 | 12:116974267 | CCTACTCTGCACATG[C/T]GTAAGAGGAAATACC | 26259 |
rs190185705 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116923067 | AAAAATTAGCTAGAT[A/G]TGGTGATGTGTGCCT | 26259 |
rs190187149 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987207 | AGAGTCCCCCGGATG[A/T]TGACGCTCCCTCCAG | 26259 |
rs190188959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952037 | TCAAAGCTCTTTGAC[A/G]TTTCTTTCCAAGCTA | 26259 |
rs190292486 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932561 | TTTCTTTTTCTTTGA[C/T]GGAGTCTCGCTGTCA | 26259 |
rs190340768 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966378 | ACCATTCACACACAC[A/G]AACATGCACACACAT | 26259 |
rs190372350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024631 | TGCAAGTGCTATTCT[C/G]ATTATTTTAGGATTT | 26259 |
rs190427265 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008163 | ACCTACTCAGTATCA[G/T]ATTTCAGTTCTTAGA | 26259 |
rs190442192 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999672 | GAGGAGCATGGGTAA[C/G]GCCCCGGTGCCCATC | 26259 |
rs190458893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973519 | TGTGCCATGTGACAC[A/G]ATGCAGTGAGAAAAA | 26259 |
rs190464803 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951034 | CAAAGCCAATTATGA[A/T]TTTCTTCTCTGGAGC | 26259 |
rs190473187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965316 | GTCACTTAATATACC[A/G]TACCAGATAATTGGT | 26259 |
rs190483611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925929 | AATCTTTGCTCTGAA[C/T]CTCCATGCTGGGTTG | 26259 |
rs190501491 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915251 | GGTCTTTTCTCCCAG[A/C]TCATCAGGTGTTTTT | 26259 |
rs190509490 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931771 | GTATTTAGGGTTTCC[C/T]ATGTTTATGTTTATA | 26259 |
rs190574184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017101 | TCAGGCATGTTGAAT[A/G]GTGTCACTGTATATG | 26259 |
rs190587782 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978536 | GTCTTTATTATAAAT[A/C]GTCAACTTCATTCAG | 26259 |
rs190664150 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937166 | CTGGAGGAATGAGTT[A/C]ACTGTTTACCGACAA | 26259 |
rs190668077 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018578 | GTGGACTTAGCACAC[C/T]GTGCTGTCTGCTGTT | 26259 |
rs190730243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944667 | GCACATGATCCTGTG[A/G]TTAAGTAAACCTTTT | 26259 |
rs190741188 | snp | A/G | 0.00795532 | 0.062565 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910590 | TTCTTCCTAATACCT[A/G]TCACTGATTTAAATG | 26259 |
rs190750548 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928671 | TGTCACCCGTCTCAC[A/T]CTTACTCTGGGGCAT | 26259 |
rs190810421 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947490 | CCGTGGGTCACTCCT[A/G]TAATCCCAGCACTTT | 26259 |
rs190810878 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001389 | TCCAGTCTAACTTTG[A/G]GCCAAACTAGAAGTT | 26259 |
rs190812996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979722 | TTCTCTAGTGTGGGG[A/C]AAAATGGGGGCTATA | 26259 |
rs190814273 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031805 | AGAGTTAAGTTCCCA[C/T]GGCATATTGCTGGCC | 26259 |
rs190819507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008770 | TCTCATGTGTGTGCT[G/T]AGAGGAGAAATCTTT | 26259 |
rs190823583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957276 | CACTTGAACCCGGGA[A/G]GTAGAGGTTGCAGTG | 26259 |
rs190828389 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995972 | TTTATTAATTCTTTT[A/G]CTGCCTGAATTAAAT | 26259 |
rs190845063 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956517 | CTGGCGTCAGAGTGA[C/G]AGGGTTTGCAGTTCT | 26259 |
rs190845771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921256 | TTAGATTCTATAGTA[A/T]TATAGTTCACTTATA | 26259 |
rs190853977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937752 | CCACAGTAGACTTGA[C/T]GTGTGAACCTGTGAA | 26259 |
rs190899239 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917168 | GGGCCATCACTATGT[C/T]AGTCTACCTCAAAAG | 26259 |
rs190909102 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920379 | TCTTGGTACCAGCCA[C/G]TGTTCCAGGCACTGA | 26259 |
rs190925252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000916 | GCGCAGGAATGACAC[A/G]AGCTGCGCTCCACCT | 26259 |
rs190943279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952628 | TTGCTGTTTCACTGA[A/G]ACATTTTTTGTTTTA | 26259 |
rs191059554 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014641 | GGTTCAGACGGCAAG[C/T]TCTGTTTACCCTTTG | 26259 |
rs191083620 | snp | C/G/T | 0.00755907 | 0.0610114 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005954 | CCAGCACAGCACCTC[C/G/T]TAACCTTTGGCTCTC | 26259 |
rs191154086 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933110 | TTCTTTCCCCTTGGA[A/G]ATTTGATTTGTTATA | 26259 |
rs191181808 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116974822 | TCTAAATGTTCTTCA[A/G]TAAAAGGAACAAGGG | 26259 |
rs191208713 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965687 | CTCAGAGGAACAAAA[C/T]TAAAGTAGCTAATGG | 26259 |
rs191240207 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922189 | GAGACAAATTGTGGA[A/T]TATAAATGGATGCTT | 26259 |
rs191387777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942979 | AGATGGGGTTTCATC[A/G]TGTTAACCAGGATGG | 26259 |
rs191411115 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025330 | CAGAATGAAACCCCA[C/T]CTCTACAAAACCGAG | 26259 |
rs191434879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025476 | ACCTCTGAGAACACA[A/G]CCTCTGAGCAGCGAC | 26259 |
rs191453323 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006297 | ATTTCAGTATGCAAG[G/T]GGTTCATGATTAATT | 26259 |
rs191455403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986464 | AAACCACGTCTCTAC[G/T]AAAAATACAAAAAAT | 26259 |
rs191459487 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116916288 | TACTGACAGTTTTCC[A/T]AAGTAGTTGTACTGG | 26259 |
rs191467402 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964264 | AGCCTGTGCCTGTGA[A/G]ACCATTAGTTCTGAG | 26259 |
rs191470711 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985720 | TTCTTCAGACTAACA[C/T]GGTGGAATCTCACCC | 26259 |
rs191473599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944391 | AAGAATCTGGTCTCC[G/T]ACTTTCTCTCATTTT | 26259 |
rs191478920 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013569 | CTCTCTGGTACTCGG[C/T]GGGTGCCTAGCACAG | 26259 |
rs191569798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925584 | TGGAAGGTCATCTAC[A/C]TGAAAGTCTGGGACT | 26259 |
rs191628514 | snp | C/T | 0.000247213 | 0.0111151 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028101 | CCTCTCCCTGTCTGC[C/T]GTTCATCCTGTGACG | 26259 |
rs191629543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994807 | GGATGCTAGATTGCT[C/T]CTGGTGTTTTGCTAT | 26259 |
rs191658675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015936 | GAAATGATGTAATCT[A/G]TGACCTTTTATGACT | 26259 |
rs191661364 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997670 | AGGGGGTTCCATCGG[C/T]TGGAAGCAGCACCAG | 26259 |
rs191676369 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975754 | ATATGAGGAAACAGC[A/G]GACAATTGAGAGGCC | 26259 |
rs191720236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923936 | GCCAGGATGATCTCC[A/G]TCTCCTGACCTCGTG | 26259 |
rs191736001 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961925 | GCCTGTAGTAGTCGG[A/G]TGTGAATGTGAGGTG | 26259 |
rs191747731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989997 | CGTTATTCCTCCCAC[C/T]CATAGTTGGATTCCA | 26259 |
rs191750776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924279 | TAGGTGGAACACTGA[G/T]AGCATCTTTATTTAT | 26259 |
rs191777816 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920015 | AGACAGCAAACCAAA[C/T]CAAATGTGTACTCAT | 26259 |
rs191800411 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029702 | GCAACCTCTGCCTCC[C/T]GAGTTCAAGCAATTC | 26259 |
rs191883925 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933848 | TCTTGGGGTGTTTTT[A/G]TTTTGAAACAGGGAG | 26259 |
rs191918835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967792 | TTTGTTTTGAGATAG[A/C]GTCTGGCTTTGTCAT | 26259 |
rs191923508 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009852 | ATCCAGTGGCTATGC[A/C/G]AGCTTCATCTTCCTG | 26259 |
rs191949623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996722 | AACTCGTGGAGACCA[A/G]TTTTCTGGGCTGTTG | 26259 |
rs191953951 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975130 | TTGAATTGCTGTATG[A/G]GAAAGGATGATGAAA | 26259 |
rs191964817 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953215 | CTACTTTCTTAGTTT[G/T]CTCAGTTTAGAATCA | 26259 |
rs191980912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936511 | TCTTGTAAGAGGGAG[G/T]CAGGACGTCAGGGAG | 26259 |
rs191985280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917430 | TGACATGAATGGGAA[A/G]TAAAATCTGGTACTA | 26259 |
rs191993150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928484 | AGCCCTTGGTTAAAT[C/T]GAGCCTGTTATTAGG | 26259 |
rs192053531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968301 | TTTTACTTTCTTGTA[G/T]ATCCTTGTATTTTAG | 26259 |
rs192114260 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020091 | AGCACACACCTGTGC[A/G]CACGGCTGCCAGTCA | 26259 |
rs192122577 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971331 | CTCTGCTGCATTTCT[G/T]CCTGGGCAACAGAGC | 26259 |
rs192129939 | snp | A/G | 0.000559947 | 0.016723 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949719 | GGGGTAAGCCAAACC[A/G]TTTCCACTGAGTGCT | 26259 |
rs192132600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001952 | GTAGGCCTGGCCTTC[A/C]TTTATTATTCCCAGC | 26259 |
rs192138693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980947 | TCACTAAAATGTTGG[A/C]TCGATCAGTCAGGGA | 26259 |
rs192151958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929359 | CTTGCCTCAGCCACC[C/T]GCATAGCTGGGATTA | 26259 |
rs192190009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981736 | CTCATGCGTCAGCCT[C/T]CTGAGTATCTGGGAT | 26259 |
rs192205498 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939449 | GTTTTGTTTAAAGCA[A/G]TGTTTCCTAAGCTCA | 26259 |
rs192214075 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912523 | GAGTTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 26259 |
rs192219725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989416 | CCTTTTATATATAGT[C/G]TATCTCTAGGATGTG | 26259 |
rs192247477 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913306 | GTAAAGAAGCAAATC[A/C/G]TGTACAGTTGACCTT | 26259 |
rs192319117 | snp | A/T | 0.0352966 | 0.128072 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910081 | TCTTTCAGATTTTTA[A/T]AAAAAAATTTTTATT | 26259 |
rs192322084 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998581 | TTTATTTCACCTTCA[C/G]AGATGTGTATGGCTT | 26259 |
rs192351068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946874 | GGTGGGAGGGGCTGC[A/G]ATTTAAGGAAAGCTT | 26259 |
rs192493851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022338 | TCTGAATAGATTATA[A/G]TGACTAAAGAAACTA | 26259 |
rs192495874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002877 | TTTATAGAGACTGTT[C/T]ACCTAGCTTTGTGCA | 26259 |
rs192506543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982525 | GGATCTGATCAAGTG[C/T]GACACTTTATAATTG | 26259 |
rs192507757 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028698 | AGTAGCAAGCTGGTA[A/G]AGCTGTACTTTTTCT | 26259 |
rs192512725 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958990 | ATAACAGGGCCCCTC[C/T]TGGCTGCTCTGGGTG | 26259 |
rs192518686 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940031 | TGAGTCGTTATCCCG[G/T]TCTTTATTGCCTGAC | 26259 |
rs192576605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002553 | GCCAACAGAAAGTCA[C/G]CTTTGGGATGGTGGT | 26259 |
rs192599533 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958155 | TTTCAATTGATGCGT[A/C]TTAAGCCCCACTTGA | 26259 |
rs192623932 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026612 | GTGCACCCCTCCCAG[C/G]CCACAGCACCTCCTG | 26259 |
rs192640450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962394 | CTGTCATTTTGGCTC[C/T]GAACTCTTTGTGTTC | 26259 |
rs192700112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934672 | GTTGCAAAAAATAGT[A/C]CAGAGAGTTCCTGTG | 26259 |
rs192720000 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976208 | ATGTTACATGATTAC[C/T]TAGAAAAGAATGTGC | 26259 |
rs192764254 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016770 | TAGTTTTGGCTCTTA[C/T]ACTGAGGTCTGTGAT | 26259 |
rs192834408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015059 | AAAACCTACAATAAC[A/C]CTCACCCCTATTCTT | 26259 |
rs192837486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945150 | GTAGTCTAAAATGTG[A/G]TATTACATGGTGGTA | 26259 |
rs192864811 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953853 | GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 26259 |
rs192866874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986122 | CTGGTAGGAGAGTGA[A/G]CAGAAAAGCCAACAC | 26259 |
rs192877190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943366 | ATTTGCTGTTATTGC[C/T]ATTGTTATTTTTGTT | 26259 |
rs192903694 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918112 | AGTTGGGAATACCTC[A/C]GTTGGCACCTGATAG | 26259 |
rs192906354 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029557 | TAAATCAGGATAAAA[A/G]CAGACATCAGTGGAA | 26259 |
rs192910294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992112 | ACCTAGCTCTGTTAA[C/T]AAACATAGTTTTCTA | 26259 |
rs192968634 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921803 | GGCTACCATTGTTAA[A/C]ATTTTGGTGTATTTC | 26259 |
rs192977864 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957513 | CTCGCTTAGTTTTAT[A/G]TGTATGTGTGAAAAA | 26259 |
rs193024131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926418 | CGATTGCAAATGAAA[A/G]TTTCTTCGTGAGTGT | 26259 |
rs193039263 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965904 | GCTGGGACTACAGGC[A/G]CATGCCACCATGCCC | 26259 |
rs193054480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970179 | CCGCTCCCTGGTCAC[C/T]GAGTTTGTCTTGAAA | 26259 |
rs193090055 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929172 | ACTTTGAGAGAGGCA[A/G]AGGTTTATGCCATTA | 26259 |
rs193095444 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011766 | CAGAGTTTGCTTGCA[A/G]TGTGAACATTTATAT | 26259 |
rs193137481 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986676 | GAATACTGTAGACCA[G/T]CAATCACTGTATGGA | 26259 |
rs193157139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011975 | TGTATTCGCTCTTAT[A/G]AGTAATCTAGAGATG | 26259 |
rs193189605 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938443 | GTGATGTGAATGATG[C/T]ACCACAACATCAATT | 26259 |
rs193232687 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116948583 | CTGTATGTTAAGAAC[C/T]GTGCTGGGCACTTAC | 26259 |
rs193251992 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991237 | CCAACAGGAATGCCA[C/T]CCACTCAAAAGTAAG | 26259 |
rs193287674 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007272 | CTAAGAAAAAAAAAA[A/T]CAGATGAATAGAGAA | 26259 |
rs193288576 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032410 | GGAGGACGTCTAGAC[A/G]GTGCACAGACAGTGG | 26259 |
rs199553840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929301 | GTGCAGTGGCGCGAT[C/T]TCGGCTTCCTGCAAC | 26259 |
rs199575101 | snp | C/T | 0.000276343 | 0.0117514 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964874 | GTAACCACAACCCTC[C/T]TCCCTATTAAGGAAA | 26259 |
rs199576840 | in-del | -/AAAC | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987693 | TATTCAGTTCATTGT[-/AAAC]AAACAAACAAACAAA | 26259 |
rs199590139 | in-del | -/GA/GTGG | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916907 | TGTGTGTGTGTGTGT[-/GA/GTGG]GTGTGAGAGAGAGAG | 26259 |
rs199638119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970495 | CGTATCAACAATGGA[C/T]GGGGGTGGGTCTCTC | 26259 |
rs199645845 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012197 | CGCACTGCCAGGGAG[A/G]TGTTCCATGCATAGT | 26259 |
rs199668216 | snp | C/T | 0.000198616 | 0.00996337 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028032 | GCTCTTTCTAGACAC[C/T]GGGGGCTGATCCGCG | 26259 |
rs199697283 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116957432 | GTGAATACGTATATA[C/T]TTGCCCTGAATTTAA | 26259 |
rs199697499 | in-del | -/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910074 | GGTTTCTCTTTCAGA[-/T]TTTTTAAAAAAAAAT | 26259 |
rs199702985 | in-del | -/CTAA | 0.0115144 | 0.0749975 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024986 | TTACGCCAGTGGCAC[-/CTAA]CTAACTGGTTAAGAC | 26259 |
rs199782924 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921818 | CATTTTGGTGTATTT[C/T]TGACTTTTTTTTTTT | 26259 |
rs199840349 | snp | A/G | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945443 | AAGGGCACCTTCCGG[A/G]TAGCAGCATCTCTGA | 26259 |
rs199846352 | snp | A/G | 4.94262e-05 | 0.00497098 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988777 | AGAACCCTCCTTTAC[A/G]CCCACGGCCCGCCTG | 26259 |
rs199872709 | snp | C/T | 0.000230787 | 0.0107397 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028136 | GGCCACTCACTACTA[C/T]GACCTCGCACTGGCC | 26259 |
rs199926759 | snp | A/G | 8.24518e-05 | 0.00642021 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028143 | CACTACTACGACCTC[A/G]CACTGGCCTTTCCCT | 26259 |
rs200011709 | in-del | -/T | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977270 | AGTATAATTTTAAGA[-/T]TTTTTTTTTCAGGAT | 26259 |
rs200013446 | snp | C/T | 1.64917e-05 | 0.00287151 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010483 | GCATTGCCTTGCAGC[C/T]CCATGGCTTCTGCCA | 26259 |
rs200040064 | snp | C/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909374 | GGCTCACACCTGTAA[C/T]CCCAGCACTTTGGGA | 26259 |
rs200068718 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030541 | GCCCCTTCAGTCTGC[A/G]TTCCCAGTTCATTTT | 26259 |
rs200131151 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944868 | TGTTTAAAATCTAAA[G/T]TCTCACATGCAATTT | 26259 |
rs200144890 | snp | C/T | 3.29701e-05 | 0.00406005 | stop-gained, synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945493 | ATCTTCCAAGAGTGC[C/T]GAGCCAAGGAACACA | 26259 |
rs200154719 | snp | A/G | 0.000710961 | 0.0188408 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985381 | CTGGCAGATAGCTGC[A/G]GAATTTGAAGTTCCG | 26259 |
rs200165772 | snp | A/C | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918002 | ACCTCAAAAAAAAAA[A/C]AACAAAAAAAAAACA | 26259 |
rs200172747 | snp | G/T | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964715 | TACATCAGGGGATGT[G/T]AGAGTGTGGGACACC | 26259 |
rs200195450 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991162 | ACCCTCCAAACACTC[A/G]TGTGGGTGAATGGCT | 26259 |
rs200205218 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011126 | TTGTTTTTTTCTTTT[C/T]CTTTTTTTTTTTTTT | 26259 |
rs200275284 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929543 | CCTGGACTGATTTTT[C/T]TTTTTTTAAAAATTT | 26259 |
rs200279515 | in-del | -/TTAA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116923703 | TAATTTTTTGTATTT[-/TTAA]TTAATTAATTAATTT | 26259 |
rs200284044 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996512 | TTCTAGTCCAGAGAA[A/C]AAAAAAAAAACTTGG | 26259 |
rs200370746 | snp | A/C | 1.67363e-05 | 0.00289272 | stop-gained, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964828 | TGAGGATAAACAGCT[A/C]GTTGGCAGTAGCAGC | 26259 |
rs200394533 | in-del | -/A | 0.0505692 | 0.150756 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022656 | TGAGGCCCTGTCTTT[-/A]AAAAAAAATAATAAA | 26259 |
rs200400298 | snp | C/G | 0.0021444 | 0.0326742 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024129 | TTTCCCTTCTCTGCT[C/G]TTCCTGGGCCTGTCC | 26259 |
rs200407002 | snp | A/G | 0.000320775 | 0.0126604 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027370 | TGGACGCCCCCTTAC[A/G]AGCTCTCTCCCACTG | 26259 |
rs200419476 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946424 | CCCAGCACTAGTGAC[A/G]TTTGGGGCCAGCTAA | 26259 |
rs200450471 | snp | A/G | 0.000624128 | 0.0176543 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027520 | GTTAGTGGTGGGGCC[A/G]GGCGAGTAAGAGACC | 26259 |
rs200508464 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116940507 | GCTTTTTTTTTTTTT[A/G]CTTCCAGTTTGTGTT | 26259 |
rs200534079 | in-del | -/GCCC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026611 | TGTGCACCCCTCCCA[-/GCCC]ACAGCACCTCCTGCT | 26259 |
rs200612816 | snp | A/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980622 | ATGAATTTATATCAG[A/T]TTTAAAAAAAAATAC | 26259 |
rs200614708 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987726 | AAACACAACAAAACC[-/A]AAAAAAACCCCAACC | 26259 |
rs200695830 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916579 | ATGTATTTTTATGTG[A/G]ACTCCTTCAGTTTTT | 26259 |
rs200725712 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945480 | TTGCTGGAAGCTCAT[C/T]TTCCAAGAGTGCCGA | 26259 |
rs200829979 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116923276 | GTAGGGCCCTTGGCA[-/T]TTTTTTTTTTTAAAT | 26259 |
rs200835846 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933024 | TAAAATTCACTTAAA[-/AG]AAAAATGTGCTGAAG | 26259 |
rs200870596 | snp | A/G | 4.94434e-05 | 0.00497184 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945467 | TCTCTGACTATTCTT[A/G]CTGGAAGCTCATCTT | 26259 |
rs200920159 | snp | A/C/T | 0.00036254 | 0.0134588 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010458 | GACGGGAGGTACGTG[A/C/T]GTTGGAAGGGCATTG | 26259 |
rs200922326 | in-del | -/A | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980625 | ATTTATATCAGATTT[-/A]AAAAAAAAATACCTA | 26259 |
rs200925694 | snp | A/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916915 | GTGTGTGTGTGTGAG[A/T]GAGAGAGAGAGAAAG | 26259 |
rs201014177 | in-del | -/A/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910088 | ATTTTTAAAAAAAAA[-/A/T]TTTTTATTTCCACAG | 26259 |
rs201024363 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936373 | TGCTGACGTCCTAAT[C/G]CCTGAATCCCACCAG | 26259 |
rs201093623 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916889 | GGTTGGCTAATTGTG[C/T]GTGTGTGTGTGTGTG | 26259 |
rs201103408 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929544 | CTGGACTGATTTTTC[C/T]TTTTTTAAAAATTTC | 26259 |
rs201116902 | in-del | -/T | 0.0267878 | 0.112589 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968132 | TGTGAACAATGTTAA[-/T]TTTTTAATCTAAAAG | 26259 |
rs201151642 | snp | C/T | 0.000199248 | 0.0099792 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027519 | GGTTAGTGGTGGGGC[C/T]GGGCGAGTAAGAGAC | 26259 |
rs201176652 | snp | C/T | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028140 | ACTCACTACTACGAC[C/T]TCGCACTGGCCTTTC | 26259 |
rs201238619 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912187 | TTTTTTTTTTTTTTT[C/T]TTTCTTTCTTTCTTT | 26259 |
rs201313585 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998722 | ATGTTTGCCTTTGTT[C/T]CAGAGGTGAAAACAC | 26259 |
rs201378141 | in-del | -/TA | 0.00517822 | 0.0506191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992445 | TTTTTTAATTCGTTC[-/TA]TTTCAGTAGCTTTAG | 26259 |
rs201392093 | snp | A/C | 0.000148291 | 0.0086095 | synonymous-codon, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985306 | CAGCCAGGACGATGC[A/C]ACCGTGGCCACAGCT | 26259 |
rs201401921 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925652 | CAGTGACTTTTTTTT[-/A]AAAAAAAGTTTGGCT | 26259 |
rs201464590 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010339 | TCCTGGTGTATAGCC[C/T]GGAAGCAGGACGCCG | 26259 |
rs201482214 | snp | A/G | 0.000889592 | 0.0210714 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010446 | AGTGGCAACATGGAC[A/G]GGAGGTACGTGAGTT | 26259 |
rs201483790 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947755 | AAAAAAAAAAAAAAA[C/T]AAAAGAAAGAAAGAA | 26259 |
rs201486098 | in-del | -/GCCAGGGAG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012188 | CATTATGTACGCACT[-/GCCAGGGAG]GTGTTCCATGCATAG | 26259 |
rs201595353 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943554 | CTTTGCTGAGGTGCT[C/G]TCTGTATATTGGGGT | 26259 |
rs201631402 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116931253 | TATATATCTGTTTTT[A/T]TGCCAGTGACATGCT | 26259 |
rs201675853 | in-del | -/AG | 0.0267878 | 0.112589 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923543 | TTTTTGTTTTGAGAC[-/AG]AGTCTCGCTCGCTCT | 26259 |
rs201675996 | in-del | -/G | 0.00914312 | 0.0669923 | intron-variant | FBXW8 | GRCh38.p7 | 12:116911713 | CAGGACAAAATATCA[-/G]TAAGTGTGGGGTTGA | 26259 |
rs201715077 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985792 | ATGAGTTCAGTGGTG[G/T]TATCCCAGTCCATCT | 26259 |
rs201718282 | snp | A/G | 1.65124e-05 | 0.00287331 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010274 | AAAGTATTTGATGTC[A/G]GCCTGGTGTGTGGAA | 26259 |
rs201810640 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936033 | GAGAGCTTCCATTGT[A/G]TATACAATAAAGACA | 26259 |
rs201854291 | snp | C/T | 0.000428513 | 0.0146312 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945440 | AGGAAGGGCACCTTC[C/T]GGATAGCAGCATCTC | 26259 |
rs201979707 | snp | C/T | 0.000692829 | 0.0185993 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964651 | TCCCCACCATAGCCC[C/T]GCTCTTCAATCTCCT | 26259 |
rs201980011 | snp | C/G | 0.00199792 | 0.0315431 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024177 | CCTCCGCAGTGGTAA[C/G]ATCGCCCTGTCGCTC | 26259 |
rs202007140 | snp | A/G | 0.000216795 | 0.0104092 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024126 | CCATTTCCCTTCTCT[A/G]CTCTTCCTGGGCCTG | 26259 |
rs202056280 | snp | C/T | 1.66189e-05 | 0.00288256 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928166 | CCAGATTTTCCTAAA[C/T]GTGTGATTAAGGTAT | 26259 |
rs202059355 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959375 | GAGGCAGAGTGGCTT[A/C]TTGGCTAAGCAGTGA | 26259 |
rs202064358 | snp | C/T | 0.000164747 | 0.0090745 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964731 | AGAGTGTGGGACACC[C/T]GCACCTGGGACTACG | 26259 |
rs202073605 | snp | C/T | 9.88826e-05 | 0.00703076 | stop-gained, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028080 | GACCAGCTGGCCTTC[C/T]AGAGCCCTCTCCCTG | 26259 |
rs202144648 | snp | G/T | 4.95225e-05 | 0.00497582 | stop-lost, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028170 | CCCTATAACCATGTT[G/T]AGGGATGTGCCTCAG | 26259 |
rs202153491 | in-del | -/A/C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955038 | CCCCTCTTGAAATGG[-/A/C/G]GGGGGGGGGGCCCTG | 26259 |
rs202244572 | snp | C/T | 0.00199792 | 0.0315431 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010441 | TGGTCAGTGGCAACA[C/T]GGACGGGAGGTACGT | 26259 |
rs367549853 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965863 | TCCCGGGATCCAGTG[A/G]TCCTCCCACCTCAGT | 26259 |
rs367570944 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000270 | CGTGAGCCACCGCAC[C/G]CAGCCTGCATCTCAT | 26259 |
rs367636944 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971711 | TAAATCTGTGCTTTT[C/G]TTTTTATGGTAATCT | 26259 |
rs367685714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918220 | GTCTTCTCTTCTCCT[C/T]TGTTCATAAACCCAG | 26259 |
rs367709612 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021901 | TCGGCTTCCATGGAC[A/G]TGACTGCCTGGTTTT | 26259 |
rs367744086 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968628 | GGATTGTTTTCTGGG[A/T]TACAGGGTAAATGCA | 26259 |
rs367751485 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116957331 | CAGCTTGGTGACAGC[A/G]AGACTGTCTCAAAAA | 26259 |
rs367756288 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002931 | CATTTTTGTAGTTCA[A/G]TTCCACGTTTCTGTG | 26259 |
rs367756554 | in-del | -/GTAGA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924175 | TGTTTTTAAGTCAGT[-/GTAGA]GTTGTCCATTTTCAT | 26259 |
rs367798347 | snp | A/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978688 | CAAGAAACCACTAAA[A/G]ACCACAAGACCAGCT | 26259 |
rs367838854 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927456 | TGGCGTTCATCTCCA[G/T]CAAGAGCAGTGTCTA | 26259 |
rs367869375 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987006 | ACTTTGAGTGAAAGG[C/T]TCCCACAAAATGCTC | 26259 |
rs367872502 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998306 | CTTTATTCACACTTG[C/T]CTAGTTCCTGTATGC | 26259 |
rs367872830 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919643 | TGTTGCCTTACTGTT[C/T]TAACTCCACCTGCCT | 26259 |
rs367899138 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969541 | AACTGGCACTTCTGA[A/G]GCAGAAACATGACAA | 26259 |
rs367913680 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031480 | GCACTTTGGGAGACC[A/G]AGGCAGGCGTATCAC | 26259 |
rs367968918 | in-del | -/AAAA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953789 | AAAAAAAAAGACAAA[-/AAAA]CAAAACAAAACAAAC | 26259 |
rs368001411 | in-del | -/AG | 0.00120096 | 0.0244753 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984501 | AGCACTGCTGCTAAC[-/AG]AGGCTTTAGGAGGAT | 26259 |
rs368052577 | snp | A/G | 0.000198236 | 0.00995382 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028045 | ACCGGGGGCTGATCC[A/G]CGCCTATGAGTTTGC | 26259 |
rs368071512 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010516 | GCCCGGCCCCCACTG[C/T]GCTGCTCACACTGCC | 26259 |
rs368077004 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983846 | AGTGCTTCGTGTGGC[C/T]GGTCTCCTTTCATCT | 26259 |
rs368081449 | snp | A/C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116993512 | AGCATTGTTTCTTAC[A/C/G]TTTGTTGGCAATTTG | 26259 |
rs368088098 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973209 | GAGGAGAGAAAAGTT[C/T]CCTTATAGTAGAATG | 26259 |
rs368102892 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021417 | TTCTGATTGTTCCCC[C/G]CAATAGGAAAAAGTT | 26259 |
rs368103739 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965380 | TCTTTTTGTACATGA[A/C]CAACTATGGATTTTT | 26259 |
rs368112159 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029171 | AAAAACCACCCTGTA[C/T]GAAGGCCACAAAGAA | 26259 |
rs368129630 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002016 | GTTTGGATGGTTTTT[-/T]GCCTGGATTTGTACC | 26259 |
rs368144498 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985386 | AGATAGCTGCGGAAT[C/T]TGAAGTTCCGAAACT | 26259 |
rs368145873 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022356 | ACTAAAGAAACTATT[-/A]AAAAAAAAAAAAAAC | 26259 |
rs368147948 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955044 | CTTGAAATGGGGGGG[C/G]GGGGCCCTGTATTAA | 26259 |
rs368238777 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949702 | GATGGTGTGGTCATT[A/G]CGGGGTAAGCCAAAC | 26259 |
rs368398600 | in-del | -/ACTT | 0.0115144 | 0.0749975 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026638 | CCTGCTCCTCCCAGC[-/ACTT]ACTTAACTCTGGGTC | 26259 |
rs368411775 | in-del | -/AG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117006651 | TGGGTCTCCTCAGAG[-/AG]GCAGGCCCCGTCTAT | 26259 |
rs368424674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932174 | TTTCGTAAGTTAAAT[A/G]GGTGTATGATTGCTA | 26259 |
rs368445739 | snp | C/T | 0.000379453 | 0.0137689 | synonymous-codon, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985246 | GACCGGAAAGTACCC[C/T]GTTCATCGTTTTGAG | 26259 |
rs368536426 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010439 | CATGGTCAGTGGCAA[C/T]ATGGACGGGAGGTAC | 26259 |
rs368712080 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116952799 | CTGGAGTGCAGTGGT[A/G]TGATCTCAGCTCACT | 26259 |
rs368719068 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936783 | TGATACGGGGATGTG[A/G]TGAGCAGAAGGATAA | 26259 |
rs368744487 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117005509 | TTGGTAATAGTGCTG[C/T]AGAGCCTCCCCTGAC | 26259 |
rs368778834 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946092 | TAACTGTCAAGAGCC[A/G]TGTTACATAAAGCTG | 26259 |
rs368810654 | snp | G/T | | | stop-gained, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985358 | TTATCCCCCAATGAG[G/T]AGGGGTACTGGCAGA | 26259 |
rs368839356 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116967005 | ATTCTTTTTTTTTTT[A/T]AAGTCATAGTTAGAA | 26259 |
rs368889689 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988749 | GTACCTGCTCAAAGC[C/T]GAAGACTCCGCCAGA | 26259 |
rs368917652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930234 | TTATATTTTTAATAT[C/T]CTAAGGAACCTGTTT | 26259 |
rs368950928 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029116 | CAAGCTGGATCCAGT[A/G]GATGCGTATGGAATT | 26259 |
rs369027100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024480 | TGCTGTCCCAGCACC[A/G]CTCTGCAGAGGAGGA | 26259 |
rs369031440 | snp | A/G | 9.90688e-05 | 0.00703737 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027446 | CTCATCACGGCCAAC[A/G]TGCCTTACCAGACGG | 26259 |
rs369078959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988064 | GCATGGTATTCCAGC[A/G]TATAGATACACTGAG | 26259 |
rs369090312 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952266 | TGTGTAAGAACACTC[-/TG]TGATGTTTGCACAAA | 26259 |
rs369100923 | snp | C/G | 0.000202679 | 0.0100647 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945343 | CAGAATTTGACATTT[C/G]TGTCACTTCTGCTGT | 26259 |
rs369201654 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017832 | GTTCCTCATTATCAT[A/G]TGGGAGTATTTAATC | 26259 |
rs369205065 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938642 | TCCATTTTAAAGTGG[C/T]TGAGATTTGCACAGT | 26259 |
rs369255305 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117015400 | TGGCCAGAATCAGAA[C/T]GTCCTCCTTTCTTTT | 26259 |
rs369335036 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910461 | TATTCCACCATATGT[A/G]TATATCAGTTTCTTT | 26259 |
rs369352345 | snp | A/G | 3.32254e-05 | 0.00407573 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928058 | TTTCTTTGATATCCA[A/G]CTGCCTTACGAATTG | 26259 |
rs369390957 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029347 | CAAAAAGCAAAATAA[A/G]ACAATTCCAGACACT | 26259 |
rs369394947 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116967114 | ACTTCCAGGCCCTCT[C/T]GCATTTTACTCGTGG | 26259 |
rs369469935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015082 | CTATTCTTTGAGGAC[A/G]GCAGGGGCCCCCTTT | 26259 |
rs369499129 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937784 | GGAACAATGAGACTT[A/C]CCCTCTGTGAGCCTT | 26259 |
rs369516963 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981980 | TGTGATAAAGACTTA[C/T]GTTAAAATCCAAAAG | 26259 |
rs369539085 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016569 | TCCCATTCTGTGGGT[C/T]GTCTTTTCGCTTTCT | 26259 |
rs369575497 | snp | C/T | 0.000230859 | 0.0107413 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964772 | CCTGGAATCAGAGGA[C/T]GAGGAGGATGAGCCT | 26259 |
rs369596114 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921486 | GAGTACCTTAGGGGA[C/T]GATCTATATTGCCTG | 26259 |
rs369613519 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010334 | TCAGATCCTGGTGTA[C/T]AGCCTGGAAGCAGGA | 26259 |
rs369697504 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915390 | TTCCCACTTTTAAAA[A/G]TTTTTAAGCTCAAAC | 26259 |
rs369751629 | snp | A/G | 3.29571e-05 | 0.00405924 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988822 | GTCTCGGCCAACCAA[A/G]TTGCTTTTGGTGTAC | 26259 |
rs369790762 | snp | G/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975232 | ATCAATGTGATGAAT[G/T]TCTCTGTCCGTTTGG | 26259 |
rs369812573 | snp | C/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909746 | GGATATATATATATA[C/T]ATAAAAATAAAATTA | 26259 |
rs369834886 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927648 | CCTCACTTTCTTGGC[C/T]GCCTGCTGCTCACCT | 26259 |
rs369855312 | in-del | -/AAGTG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965539 | CTCCGTTATGTTGTG[-/AAGTG]TTGAATCTCCACAAG | 26259 |
rs369900260 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936733 | GTTTTAAGCAGCTAA[A/G]TTTGTAGTAGTTTGT | 26259 |
rs369902843 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031940 | AACAAGATAATTACC[C/T]AATTTTTGGTGACTC | 26259 |
rs369981569 | snp | C/T | 8.24002e-05 | 0.0064182 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964693 | GTGTGTCGTTCTCTT[C/T]CAGATATACATCAGG | 26259 |
rs370044447 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989342 | TAGGTGTTTAGCTTG[C/T]TTTCACTGTGTTGGC | 26259 |
rs370066094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939878 | CTGTGCTTCATGATT[G/T]CCCAGTGCTCAGACA | 26259 |
rs370112379 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986780 | GCACAGACTGGAAGC[C/T]TTTTGAACTAGTTTA | 26259 |
rs370115627 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116952898 | GTGTGCCACCACACC[-/C]AGCTAATTTTTGTAT | 26259 |
rs370158191 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969632 | TAAGACAATAAAATG[A/G]GTTAATGAACTTCAG | 26259 |
rs370168349 | snp | A/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987100 | ACGCCCCTGAATGGC[A/T]GTGGCAGTGTTCCCA | 26259 |
rs370169098 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980580 | TTCATTGCTAGGTCC[A/G]CAGTATGATAACACT | 26259 |
rs370182050 | snp | C/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910061 | ACCTTCCCTTGGCTG[C/G]TTTCTCTTTCAGATT | 26259 |
rs370195521 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117015242 | TCTTCCCCTGTACAG[C/T]CACTTCCATGGGTTT | 26259 |
rs370198079 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117005202 | AGGAGTGGAGGAAGG[C/T]GTTAAAGCACTAAAA | 26259 |
rs370199917 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031334 | CCAGGATCCAGGAGA[A/C]CCGCAACATGGTACA | 26259 |
rs370220650 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116952279 | TCTGTGATGTTTGCA[A/C]AAATGATAAATTCAC | 26259 |
rs370234559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958018 | AGGGCCACAGCTACA[A/G]TAACTCTGCATAATC | 26259 |
rs370280395 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030243 | GAGCTGCGACTGGGA[A/T]GCGTCACCTTCCCGT | 26259 |
rs370299783 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976354 | GCTATTTGTCTTCAA[A/G]CTATTCCCCACCTGC | 26259 |
rs370310036 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012668 | ATAGCTTATGTTTTA[G/T]GTCAAAAGTGGGAGA | 26259 |
rs370351747 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971403 | GAGGGGGTTTTGGTG[C/T]TTAAGAAATCCTTTT | 26259 |
rs370355248 | snp | A/G | 4.942e-05 | 0.00497071 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010374 | TTGAAGCTGGGTAAC[A/G]TTCTCCGTGACTTCA | 26259 |
rs370410629 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924178 | TTTTTAAGTCAGTGT[A/T]GTCCATTTTCATGTT | 26259 |
rs370426742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013883 | TCACTAAGGAAAAGT[C/G]TGCAGGAAGTAATCA | 26259 |
rs370466421 | snp | A/G | 1.65031e-05 | 0.00287251 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949569 | CGATGCTTGGCTTTC[A/G]GGCTGTCCCGAGAGC | 26259 |
rs370486587 | snp | C/T | 5.84778e-05 | 0.00540699 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985183 | ATTTAAAATTGTTAC[C/T]TGCATTGTTTCTTGC | 26259 |
rs370579503 | in-del | -/AAAAG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947750 | CAAAAAAAAAAAAAA[-/AAAAG]AAAAGAAAAGAAAGA | 26259 |
rs370605033 | in-del | G/TT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922812 | AGTGTGTGTGTGTGT[G/TT]TTTTTTTTCCCTTGA | 26259 |
rs370607329 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990737 | GGATCCTTCAGATAC[A/G]GATGTAAGGCAGTGG | 26259 |
rs370638083 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968721 | AGTTTTGCCAACAAA[A/G]TATGTTTCCAGCTTT | 26259 |
rs370650207 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004790 | TTTCCCCAGCTCTCC[A/T]GTTTCCCCAGCTCTC | 26259 |
rs370652093 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116948370 | TCCACTTGTAGGACA[C/G]CTCCACGTGGATGTG | 26259 |
rs370653927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995766 | ATATGATTGTAAAAG[A/G]AAACAAAGGTAAAAG | 26259 |
rs370656266 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968406 | ATTTACTTTACATGA[C/T]TCCACACCTTGGCTT | 26259 |
rs370661477 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001177 | CTGCTAAGCATGTCT[C/G]TGCCAATACCTCATG | 26259 |
rs370691126 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926585 | ACATTAAACCAATGA[C/T]TTTCCATTATTTTTT | 26259 |
rs370725158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929631 | ATTTTTGAAATATCT[A/G]TGCATTGTGGAATGG | 26259 |
rs370725910 | in-del | -/TGCAGTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956530 | AGAGGGTTTGCAGTT[-/TGCAGTT]CTTTGTAGACAGAGA | 26259 |
rs370802764 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990443 | GCTCTAAAAAAACTT[G/T]CTTTTCCCATCCCTG | 26259 |
rs370815664 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928938 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGACTGCGG | 26259 |
rs370843691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916826 | ATGGGTGAGCTCACT[C/T]GTGTGTCTGAGGTTA | 26259 |
rs370862920 | snp | C/T | 1.66001e-05 | 0.00288094 | intron-variant | FBXW8 | GRCh38.p7 | 12:117028018 | GTCACCATCTTTGTG[C/T]TCTTTCTAGACACCG | 26259 |
rs370891359 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986582 | GCAGTGAGCCGAGAT[C/T]GCCACTGCAGTCCAG | 26259 |
rs370914359 | snp | A/G | 1.64827e-05 | 0.00287073 | synonymous-codon, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945429 | GCTGTGCCAGCAGGA[A/G]GGGCACCTTCCGGAT | 26259 |
rs370924764 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025504 | GACATGGTCTTTATG[A/G]AAGTGCAAGGTCAGC | 26259 |
rs370977239 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963617 | TCAAAAACAAACAAA[A/C]GAAAACAAAAACCAA | 26259 |
rs371031051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912437 | CCAAGTGATCCTCCC[A/G]ATTGAGAATCATTCT | 26259 |
rs371129545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009027 | AGCCAAGATCGCGGC[C/T]ACTGCACTCCAGCCT | 26259 |
rs371138207 | in-del | -/GT | 0.00635498 | 0.0560099 | frameshift-variant, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010391 | TCTCCGTGACTTCAC[-/GT]GTGTCAACCTCAGCG | 26259 |
rs371150811 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028356 | CTGGGGCAAGCTGGC[A/G]TGTGCCAGGGCTCGA | 26259 |
rs371180862 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001977 | CCCAGCACCTACGGA[C/T]GTGCTGAGAGAGAGA | 26259 |
rs371238444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008745 | GCTGACAAGAAGAAA[C/T]GCACATCACTCTCAT | 26259 |
rs371238676 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941157 | TTGTTAGATCAGACT[C/G]ATGGGGGAGGTCAGC | 26259 |
rs371253473 | in-del | -/TTGTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116997817 | TTGTTTTTGTTGTTG[-/TTGTT]TTGTTTTTTTGAGAG | 26259 |
rs371258911 | snp | G/T | 0.00017991 | 0.00948276 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027553 | CTTAGTTTGACTGAT[G/T]TATAGAACCCCACCC | 26259 |
rs371269838 | in-del | -/AAGT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008713 | AATCTGTATCGTGGT[-/AAGT]GATAAATGTATAGGC | 26259 |
rs371323948 | snp | A/G | 8.23811e-05 | 0.00641746 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024208 | TCCGCCCATCAGCTC[A/G]GGGTCTCTGCTGTGC | 26259 |
rs371359255 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939939 | CTGGGTGTCATGGGT[A/G]GGCTCAGCTGTGGAC | 26259 |
rs371364870 | snp | C/T | 3.34459e-05 | 0.00408924 | synonymous-codon, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985219 | AGGGTTTCTTAATAT[C/T]TGGGATTTAAGGACC | 26259 |
rs371366780 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962418 | TGTGTTCAGGGAGCT[A/G]GGGGGCTGGAGCTGA | 26259 |
rs371416783 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920546 | ATAGAGTGTATCTGC[C/T]AGGGGAGGGGCTGTA | 26259 |
rs371418929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926543 | TGATGAGTGAAGCCA[A/G]TTAGTTGTGGGAGGG | 26259 |
rs371463745 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032316 | ACACACTCAGACTGC[A/G]ACCAGACACCAACAA | 26259 |
rs371583699 | snp | A/G | 1.95842e-05 | 0.00312917 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027531 | GGCCGGGCGAGTAAG[A/G]GACCATCTTAGTTTG | 26259 |
rs371636900 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914679 | TCAGGAGTTCGAGAC[C/T]AGCCTAACCAACAAG | 26259 |
rs371654779 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951211 | CTGTGGGTCGAGAGG[A/C/T]TCCTGGTGGCTCCTC | 26259 |
rs371666072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013765 | TTATTTATTTTTTAT[G/T]ATCATCAGTGGTGTT | 26259 |
rs371676447 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029952 | CAAAATATACAACTC[A/T]TGATAAAACATAAAG | 26259 |
rs371681424 | snp | C/G | 0.0763149 | 0.179815 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955049 | AATGGGGGGGGGGGG[C/G]CCTGTATTAAGCATC | 26259 |
rs371693667 | snp | A/G | 1.64925e-05 | 0.00287158 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988668 | CTTTTAACAGGTTCA[A/G]TACCTTGAAATAGTT | 26259 |
rs371718656 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937635 | CCTTGACCAGGGTCA[G/T]TGGTGTGTTGGGGGC | 26259 |
rs371808680 | snp | A/T | 6.59337e-05 | 0.0057413 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964683 | TTGGAACCAAGTGTG[A/T]CGTTCTCTTCCAGAT | 26259 |
rs371809248 | snp | A/G | 4.94181e-05 | 0.00497057 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949706 | GTGTGGTCATTGCGG[A/G]GTAAGCCAAACCGTT | 26259 |
rs371843708 | snp | A/G | 1.7067e-05 | 0.00292117 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027360 | GCAGGCCCAGTGGAC[A/G]CCCCCTTACGAGCTC | 26259 |
rs371844474 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978653 | GAGGATGGGAGCTCG[C/T]GGCTGAAATAATTTC | 26259 |
rs371845259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936364 | TCCCAAATATGCTGA[C/T]GTCCTAATCCCTGAA | 26259 |
rs371858073 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117006093 | CTGGACAGACAGTGC[C/T]GGGCTTCTGGGGAGC | 26259 |
rs371868989 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014975 | CAGAGTTCTACCTGC[C/T]GGCATCGCCGCCACC | 26259 |
rs371883999 | snp | A/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978789 | GGAAAAGATCAAAGG[A/G]GAGGGAAGAGTATAC | 26259 |
rs371974524 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955051 | TGGGGGGGGGGGGCC[-/C]TGTATTAAGCATCTG | 26259 |
rs371991477 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924325 | ACATTATAATTGTAC[A/G]TATTTATGGGGCACG | 26259 |
rs372022897 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965594 | AAAAGTTGGGACCAC[A/G]GCATATTTCAGAATG | 26259 |
rs372043633 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965535 | TATCCTCCGTTATGT[C/T]GTGAAGTGTTGAATC | 26259 |
rs372064597 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966623 | ATGTGCAGGGGTGCT[A/G]CTGCTGGTTTTATAT | 26259 |
rs372153349 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937126 | AGAGAGTCAACAAGG[A/G]CTCCATGGTGTTTGC | 26259 |
rs372175983 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980664 | GTGAATTTCCTTGAC[C/T]CTGACAGGCATTAAC | 26259 |
rs372180177 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959846 | TCAACCTTGCCAAGT[A/G]TAGAAAAGACTGGGA | 26259 |
rs372212615 | snp | C/T | | | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978212 | CCTTTTTCGTGACCC[C/T]CCGTGGTTTAGCTGT | 26259 |
rs372248535 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116948429 | ATTCCTTGGATTAAG[G/T]TAAGACCATCATGCA | 26259 |
rs372363018 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984266 | CCAGTGGACATCCCC[A/G]GAGTTACTGGTGCCT | 26259 |
rs372402119 | snp | A/G | 3.34515e-05 | 0.00408958 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028206 | AGCAAGGAGAAAAAT[A/G]GGAAGAACCAGTTTT | 26259 |
rs372403984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952883 | GCTGGGACTACGGGC[A/G]TGTGCCACCACACCC | 26259 |
rs372460546 | in-del | -/AAAC | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013270 | GAAAAACTAAAAAAT[-/AAAC]AGAGTCTGATGAAGA | 26259 |
rs372502629 | snp | G/T | 1.65089e-05 | 0.00287301 | stop-gained, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945391 | TGGAAGGTGATTGCA[G/T]AGGATGAGGTGCTGT | 26259 |
rs372519246 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985337 | TCTGCTTTTGATGTC[A/G]TGATGTTATCCCCCA | 26259 |
rs372586839 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933029 | ATTCACTTAAAAAAA[-/A]TGTGCTGAAGTGTAA | 26259 |
rs372615177 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970781 | GCTTGCGAGAAGGCT[A/G]AGGCAATTGATGGAT | 26259 |
rs372624291 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925715 | GCTTTGAAACAGTGG[C/T]TGCCCTTCAGAACTT | 26259 |
rs372632817 | in-del | -/A | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983989 | GGATTTGAACTCAAA[-/A]TAGTCACAAACTGTT | 26259 |
rs372702199 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999552 | TCCCCTTCCTGGCTC[A/G]CCCCTGCCCTTTCCC | 26259 |
rs372725345 | snp | C/T | 9.89446e-05 | 0.00703296 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949578 | GCTTTCGGGCTGTCC[C/T]GAGAGCAGTCTAAAC | 26259 |
rs372741448 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020095 | CACACCTGTGCGCAC[A/G]GCTGCCAGTCAGCCT | 26259 |
rs372743201 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996109 | GCTCTTAGCATCATT[A/C]TATGTATTTGGACAT | 26259 |
rs372743666 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969707 | CCTCGCTGGTCTACA[C/T]GCACATTCTCGGTGG | 26259 |
rs372772196 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969896 | ACCCTCTGGCCTCAT[A/G]TTTCTTCTGCCTTGT | 26259 |
rs372799144 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924964 | CTAGTATCCTCCTCA[A/T]GTAGGGGAGAGGAAG | 26259 |
rs372804799 | snp | A/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975954 | GTTAAATGCAAATAA[A/T]ATCTGTAGATTAAAT | 26259 |
rs372808387 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945671 | TCAGCTGTTGGTGAC[A/T]TGTTGCCCATTTTGT | 26259 |
rs372814319 | snp | A/G | 0.000115322 | 0.00759261 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010351 | GCCTGGAAGCAGGAC[A/G]CCGCCTCTTGAAGCT | 26259 |
rs372814647 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116916028 | AAACAGCACATACTC[A/G]TGTGTCTTTGAGTTC | 26259 |
rs372826386 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031116 | TGCTTTATGATGTCC[A/G]TAGTTGTTCTAATAT | 26259 |
rs372877140 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029147 | TCAAATACACATAGA[C/T]GATGCACAAAAAACC | 26259 |
rs372916639 | snp | A/G | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988852 | CAGGGTCTGGGATGG[A/G]TGTACGAAGGAAGCA | 26259 |
rs372954122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954605 | TCTATATAAGTATAT[A/G]AAATAAAGAGTTAAA | 26259 |
rs372985533 | snp | G/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982172 | AGCAAAATGGTAGAT[G/T]AAACCCAACCTTATG | 26259 |
rs373012240 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999531 | TAATCCCTCCCCGAG[C/T]GCATTTCCCCTTCCT | 26259 |
rs373012381 | snp | G/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910642 | TCTCCCTACTTAAAC[G/T]CATGCTCCAAGACGT | 26259 |
rs373014847 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912191 | TTTTTTTTTTTCTTT[C/T]TTTCTTTCTTTTCTG | 26259 |
rs373025038 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938410 | TTTCTACGGAATAAG[A/C]ACTGTGACCCGGGGT | 26259 |
rs373043679 | snp | C/G | 4.95389e-05 | 0.00497664 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985372 | GGAGGGGTACTGGCA[C/G]ATAGCTGCGGAATTT | 26259 |
rs373050259 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008992 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGCTTGC | 26259 |
rs373057761 | snp | G/T | 4.22422e-05 | 0.00459558 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985177 | AAGTAAATTTAAAAT[G/T]GTTACCTGCATTGTT | 26259 |
rs373066028 | in-del | -/CAAA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953814 | AAACAAACAAACAAA[-/CAAA]AAACAAGAAAAACAA | 26259 |
rs373082644 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024523 | AATGGCGCTGGTCAG[C/T]GGGGATGCAGTTCCT | 26259 |
rs373113624 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938915 | TGGAGAAGTAGCCCC[A/G]GTCTGGGTGCATCCA | 26259 |
rs373125235 | snp | A/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909578 | AGCTTCCAGCGAGCC[A/G]AGATCGCGCCACTGC | 26259 |
rs373132395 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912451 | CAATTGAGAATCATT[-/C]TTTTTTTTTTTTTTT | 26259 |
rs373191975 | snp | A/C/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975520 | CTGAAATGGTGGTAG[A/C/G]GGGGACACAACATTC | 26259 |
rs373213609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117004561 | TAGCCTTGCAGGTGG[C/T]GTAAACTCAAACCCA | 26259 |
rs373237066 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968310 | CTTGTATATCCTTGT[A/G]TTTTAGTATTACAAG | 26259 |
rs373272738 | in-del | -/ACAGACCCTTTCA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026610 | TGTGCACCCCTCCCA[-/ACAGACCCTTTCA]GCCCACAGCACCTCC | 26259 |
rs373283900 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027461 | GTGCCTTACCAGACG[A/G]TAATGCGAAACGCCG | 26259 |
rs373298730 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116967434 | TGCTAGGTTGGAGGC[C/T]ATGGCTGCAGGCTTT | 26259 |
rs373301900 | snp | A/G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970481 | TTCTCATTTACTGAC[A/G/T]TATCAACAATGGACG | 26259 |
rs373302070 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922654 | AGAATTAGTCTTACA[G/T]TAGCACATAGGAATA | 26259 |
rs373312054 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026419 | AAGCCTGCCCTCCCT[C/T]CCCGGGTCTTTCTCA | 26259 |
rs373334800 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007290 | GATGAATAGAGAACT[G/T]TCTGCTAGAGTTCTT | 26259 |
rs373361925 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964707 | TCCAGATATACATCA[A/G]GGGATGTGAGAGTGT | 26259 |
rs373363586 | snp | A/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910136 | GTATTTGGTTACATG[A/G]GTAAGTTCTTTAGTG | 26259 |
rs373380437 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027250 | GTGAGACACTGCTTC[C/T]ATGGGGGCCCTGTTC | 26259 |
rs373381027 | snp | A/G | 6.78783e-05 | 0.00582534 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027987 | GGGGTGAGGGCCAGC[A/G]AGGCAGCCCTGACCT | 26259 |
rs373469975 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921790 | ATAATTGCTTAGAGG[A/C]TACCATTGTTAACAT | 26259 |
rs373499328 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967510 | AGGTTTCACCAGTTT[A/G]TAGTGTCACCAAAAG | 26259 |
rs373527147 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004516 | GGTATGTTACCAACC[-/C]GAAAATACTTTATTA | 26259 |
rs373532018 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913881 | TTCCTGGAATTCATT[-/T]CCCTGGTCTCCTCTG | 26259 |
rs373550067 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949570 | GATGCTTGGCTTTCG[C/G]GCTGTCCCGAGAGCA | 26259 |
rs373651338 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026276 | GTCCACCAACACTTT[C/G]CTTCAGTCCTCCAGG | 26259 |
rs373653320 | snp | C/T | 0.000181568 | 0.00952632 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988857 | TCTGGGATGGGTGTA[C/T]GAAGGAAGCAAGGTA | 26259 |
rs373654547 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969663 | TTCTCTGGTTGTGCC[A/T]AAGTGAGGCTCTGTA | 26259 |
rs373670573 | snp | C/G/T | 5.10368e-05 | 0.00505136 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945315 | TTTGGATGACAAGGG[C/G/T]CTTCTCTAATTGCAG | 26259 |
rs373698678 | in-del | -/ATGCTGTTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014706 | AGCTGTTCAATTTCT[-/ATGCTGTTT]TTGGTCTGCGCATGT | 26259 |
rs373731829 | snp | C/T | 3.32237e-05 | 0.00407563 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928063 | TTGATATCCAACTGC[C/T]TTACGAATTGGCAAT | 26259 |
rs373815324 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017885 | GAGTTGTGACCCCCC[-/C]AATTACAGAGTCTCA | 26259 |
rs373830111 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009854 | CCAGTGGCTATGCAA[G/T]CTTCATCTTCCTGGT | 26259 |
rs373834062 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971493 | TCACAGACAGGCCAC[A/G]GAGACTGTATTAGGG | 26259 |
rs373839010 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992163 | TTAGCAAAAGCTTAT[C/T]TGTCTAATCTTTTTT | 26259 |
rs373876548 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971783 | TGTGCTGTGGGATCT[C/T]GGTACCAGAATTTAC | 26259 |
rs373880041 | in-del | -/TAAC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020159 | GTACCATAATTGCTT[-/TAAC]TAGCACTCAGTTGAA | 26259 |
rs373883491 | in-del | -/GAGT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992747 | TTCCTTTTTATGGTT[-/GAGT]ATTATTCCATGGTGT | 26259 |
rs373892193 | in-del | -/TCTTC | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918206 | GCACTTTCTCTGTTG[-/TCTTC]TCTTCTCCTCTGTTC | 26259 |
rs373898576 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970815 | GGAGAAGTTGATTTT[G/T]TTCAAGGCCTTTGTT | 26259 |
rs373911089 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007967 | ACTCTTCAGATAGTT[C/T]GGATTCGTTTGAATT | 26259 |
rs373975508 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947470 | ACATGAAAGGCGGCC[C/T]GGCACCGTGGGTCAC | 26259 |
rs373984207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969167 | AAGATGATTACTCAA[C/T]GCCTGGGTAAAATCT | 26259 |
rs374044450 | snp | C/T | 3.32917e-05 | 0.0040798 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027391 | TCTCCCACTGCCTTC[C/T]AGGCACCCGGTGCAG | 26259 |
rs374116125 | in-del | -/GAGA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001991 | ACGTGCTGAGAGAGA[-/GAGA]TTGGCCGGTTTGGAT | 26259 |
rs374144630 | snp | A/G | 3.29636e-05 | 0.00405964 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985353 | TGATGTTATCCCCCA[A/G]TGAGGAGGGGTACTG | 26259 |
rs374165542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916630 | AAGCTGGGCATGGTG[C/G]CACATGCCTGTACTC | 26259 |
rs374180807 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983745 | ATAGAAGGGGAATTA[A/G]CATTGATAGATTAAA | 26259 |
rs374217538 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031708 | GACAGAGCGAGACTT[C/T]GTCTCAAAAAAAGAA | 26259 |
rs374219494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983240 | TTGGCATGGGAGAGC[C/T]GATCTCCCATCTGAT | 26259 |
rs374228884 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016487 | TATTATTGAGTTATT[A/G]GAGTATTTTTTTAAT | 26259 |
rs374379928 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928787 | CAGATTCAGATTCAG[A/G]AAGTCTGCGGTGGGG | 26259 |
rs374395525 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032934 | CAGACACTGGCCGCC[A/G]CAAACCCACTTTGTT | 26259 |
rs374397512 | snp | A/C | 0.00119737 | 0.0244387 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911068 | CTGGATGAGTTCCGT[A/C]GGCGCTGGCAGGAGG | 26259 |
rs374407199 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937301 | TTTGGAAGCTGTCAG[C/T]CACATTGATGGTATT | 26259 |
rs374444844 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954863 | CGTGCCTCCTGCCCC[C/T]CTTCCTTCCTCCCCG | 26259 |
rs374450274 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962917 | TTCTGGTATAGGGTT[C/T]CTCATTGAGAAGGGT | 26259 |
rs374462591 | snp | A/C/G/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027569 | TATAGAACCCCACCC[A/C/G/T]CCCCGCCGTGACACA | 26259 |
rs374502340 | snp | A/G | 1.7373e-05 | 0.00294724 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985200 | GCATTGTTTCTTGCT[A/G]CATAGGGTTTCTTAA | 26259 |
rs374550335 | in-del | -/AACT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117024992 | CAGTGGCACCTAACT[-/AACT]GGTTAAGACATTTCC | 26259 |
rs374595037 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028358 | GGGGCAAGCTGGCGT[C/G]TGCCAGGGCTCGAGT | 26259 |
rs374653714 | snp | A/C/G | 0.000164777 | 0.00907532 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024274 | GAAGGCCTGGTGTCC[A/C/G]TGTGGGATTATCGGA | 26259 |
rs374687323 | snp | A/G | 5.06256e-05 | 0.00503093 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945543 | GGTGGGCAGTGGCCA[A/G]TATCATTACCTGTGA | 26259 |
rs374714495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936470 | GATTATCTTGGATTA[C/T]ACAGGTGGGTCCAGT | 26259 |
rs374728605 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117006854 | TTATTTATTTTATCT[A/C]AAAATTATAAACAAT | 26259 |
rs374795754 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988741 | GATCTGATGTACCTG[C/T]TCAAAGCCGAAGACT | 26259 |
rs374802445 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021877 | CTGTGACGTTTCATC[C/T]CGTTGCTTTCGGCTT | 26259 |
rs374842368 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979792 | CAAAAAAAAAAAAAA[A/C]AAAACACTTGCTTCT | 26259 |
rs374892442 | in-del | -/GAC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921820 | TTTTGGTGTATTTCT[-/GAC]TTTTTTTTTTTTTTT | 26259 |
rs374903223 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013945 | TGGGGTTTATTAAGC[A/G]TTTAGAATCTGTATA | 26259 |
rs374907142 | snp | C/T | 0.000395537 | 0.0140575 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964684 | TGGAACCAAGTGTGT[C/T]GTTCTCTTCCAGATA | 26259 |
rs375007554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927032 | TGTAAGCAGTAAGTC[A/G]CTGATGTCAGCCAAA | 26259 |
rs375061882 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928969 | GCATGTGCTGCCATG[C/T]CCAGCTAATTTTTGT | 26259 |
rs375115562 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023408 | AATTTGATTTACTTT[C/T]AGCCTTTGGCTTATT | 26259 |
rs375153788 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959907 | TCCTCATTTGGAAAA[A/G]ACTTCTTTCTTCTTC | 26259 |
rs375233574 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921422 | TAGCATTGTTTGTTT[A/G]GAGAAATGTTTTCCA | 26259 |
rs375255308 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116914420 | AAACCCCATCTCTAC[A/G]AAAATTGGCCAGCGT | 26259 |
rs375263486 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937386 | GTTCAGGGATGGAGC[C/T]CTGGTGCTCCACAAG | 26259 |
rs375267302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016473 | TTGGGCTGTCTTTAT[A/G]TTATTGAGTTATTAG | 26259 |
rs375271319 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116999194 | CACATCTGAGCGGTC[A/G]CATCCCAAACTAAGG | 26259 |
rs375370998 | snp | C/T | 0.000412184 | 0.01435 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010479 | AAGGGCATTGCCTTG[C/T]AGCCCCATGGCTTCT | 26259 |
rs375421298 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984309 | TTCTAATAAGTCGCC[A/G]CGTGGTACTGATGCT | 26259 |
rs375451573 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116945308 | ATTGATTTTTGGATG[A/C]CAAGGGGCTTCTCTA | 26259 |
rs375453590 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002163 | CACAGCCCGCAGCAG[C/T]TGGCACTGCCTGCCC | 26259 |
rs375481391 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988788 | TTACGCCCACGGCCC[A/G]CCTGTCACATGTCTA | 26259 |
rs375530922 | snp | A/G | 0.000296482 | 0.0121718 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010399 | ACTTCACGTGTGTCA[A/G]CCTCAGCGACAGCCC | 26259 |
rs375636915 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970028 | GCATTAGATAAAGCA[C/G]GCGAAGGTTCTGAGT | 26259 |
rs375661630 | in-del | -/AAGA | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938207 | GTTCTCCTTTAAAAG[-/AAGA]AAGAAAAGCACCCTC | 26259 |
rs375668889 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009855 | CAGTGGCTATGCAAG[A/C]TTCATCTTCCTGGTC | 26259 |
rs375672019 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117006038 | AGCTTTTAAAATGCT[A/C]TTGTCTTGTAAGGAA | 26259 |
rs375716714 | snp | C/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984803 | CAAAAAAGCAGCCTG[C/G]GCAACATAGTGAGAC | 26259 |
rs375728596 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031629 | TGAGGCAGGAGAATC[A/G]CTTGCAGCCAAGAGG | 26259 |
rs375753222 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960806 | GACTTTACAGTCAAG[A/T]TGAGGAGACGATCAA | 26259 |
rs375764608 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116974489 | GATCCCCTAAAAAAA[A/G]TTGGAAAGCAAGCCA | 26259 |
rs375786076 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912605 | GCTGGGACTAACAGG[C/T]GCCCACCACCACGCC | 26259 |
rs375796582 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116997929 | CAAGCAATTCTCCTG[C/T]CTCAGCTTCCCCAGT | 26259 |
rs375824760 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970796 | AAGGCAATTGATGGA[C/T]TGTGGAGAAGTTGAT | 26259 |
rs375856279 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955396 | AACTTGAGAAAAATT[G/T]ATGTTCATAAGTCAC | 26259 |
rs375864228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993251 | TGGGATTACAGGCAC[A/G]TGCCACCACGCCTGG | 26259 |
rs375898221 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030156 | TGAAGGTTCTGGAAG[A/G]TTTTTCAGATTGCTT | 26259 |
rs375930820 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953983 | GCTGGGCGTGGTGGC[A/G]GGCACCTGTAATCCT | 26259 |
rs375958992 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117015024 | GACTGTCCTTGGGGC[A/C]CAGCCACAAGAAAGA | 26259 |
rs375964615 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944062 | TAGGCTGCCGGTTTT[-/T]ACAGCTGCTATCTTC | 26259 |
rs375982135 | snp | A/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910657 | GCATGCTCCAAGACG[A/T]CAGAGTTTTTGTTTT | 26259 |
rs375984294 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930457 | TTTTGAGAAATGTCT[A/G]TTCAGGTCCTTTGCT | 26259 |
rs376002368 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990857 | TCCTTGGTTAAAAAT[A/G]TATAGTCCCTGGCTG | 26259 |
rs376064436 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985244 | AGGACCGGAAAGTAC[C/T]CTGTTCATCGTTTTG | 26259 |
rs376094234 | snp | A/G | 0.000116097 | 0.00761807 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027400 | GCCTTCCAGGCACCC[A/G]GTGCAGCACATCTCA | 26259 |
rs376107596 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983297 | GCATATTTTTCTCTT[C/T]TGAGTCAGGATGGAA | 26259 |
rs376113045 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962906 | CAGGGTATGTGTTCT[G/T]GTATAGGGTTCCTCA | 26259 |
rs376126929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982574 | AAGATGAAGACACAA[C/T]AGGCTTTCAGGAGAG | 26259 |
rs376159680 | snp | C/G/T | 3.32487e-05 | 0.00407719 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027492 | ACCTGGACAGCTTCA[C/G/T]TACTCACAGGAGGTT | 26259 |
rs376186920 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949741 | CTGAGTGCTCTGCAT[C/G]TGAAGGTCTTTCATT | 26259 |
rs376193964 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996378 | GCTCACACTCATCAC[A/G]AGTTGAAATATCTGT | 26259 |
rs376258588 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116999650 | CTCAGAGCACTGGCT[G/T]CGTGGCGAGGAGCAT | 26259 |
rs376292994 | snp | C/T | 0.000164756 | 0.00907472 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964745 | CCGCACCTGGGACTA[C/T]GTAGCCCCCTTCCTG | 26259 |
rs376301881 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116934899 | ATCACGAGAATCTCT[C/T]GTGCTACTCTTTCAC | 26259 |
rs376322819 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910391 | ATAATAGTCTCCAAT[C/T]CCATCCAGGTTGCTA | 26259 |
rs376343655 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925473 | AGCATTTGGTCTCCT[C/T]ACCTTGGAGGAGTCT | 26259 |
rs376401839 | snp | A/G | 8.27726e-05 | 0.00643268 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945375 | TTAGGTGAGCAAGAC[A/G]TGGAAGGTGATTGCA | 26259 |
rs376410085 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927715 | CGGTGATTCCTGTGC[C/T]GTATACCAGGCTGGA | 26259 |
rs376410721 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116961177 | ATTTTTGCATTTTTA[A/G]TAGAGACGAGGTTTC | 26259 |
rs376504740 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970575 | CTGTAGAGACTAGGT[A/G]CTTCTAAAGTTTTAC | 26259 |
rs376512475 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979094 | TCCTTGTTCCCATGA[C/T]GAAGAATATAAATAT | 26259 |
rs376543454 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922282 | AAGACACAGGTGAAA[C/T]TGAAACTCATCTATT | 26259 |
rs376563559 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116948776 | TTTATTTTTTTAGAG[A/G]TAGGTTCTCACTCTC | 26259 |
rs376569151 | snp | A/C/T | 6.76743e-05 | 0.00581663 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027369 | GTGGACGCCCCCTTA[A/C/T]GAGCTCTCTCCCACT | 26259 |
rs376682481 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993902 | TCTTGGTTAATTTTT[A/G]TATATGGTGAGAGAA | 26259 |
rs376688645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973483 | CATTTAACATCATCA[A/G]TAATGGTAGAATTGA | 26259 |
rs376709749 | snp | A/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986048 | TGGTGTTAAGAAGGA[A/G]GTGCTCAAATCTGTC | 26259 |
rs376715753 | in-del | -/TGCCTGCC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001348 | CTGATTTTAGCTGCC[-/TGCCTGCC]CTCTTCTAGAAGCTT | 26259 |
rs376730495 | snp | A/G | 8.25471e-05 | 0.00642392 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988858 | CTGGGATGGGTGTAC[A/G]AAGGAAGCAAGGTAC | 26259 |
rs376757459 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933608 | TTGTTGTTGTTGTTA[A/G]CCCAGTTGTTAGAGC | 26259 |
rs376796829 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011517 | TCCTCAGTGTGTGTG[G/T]GGGGCACGCACTGGG | 26259 |
rs376831210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970908 | CACCCTTAGGTCCAG[G/T]AATCTAGTCTTCATA | 26259 |
rs376890398 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912187 | TTTTTTTTTTTTTTT[-/C]CTTTCTTTCTTTCTT | 26259 |
rs376899001 | snp | C/T | 3.30841e-05 | 0.00406706 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027414 | CGGTGCAGCACATCT[C/T]ATTCAGCAGCCACAG | 26259 |
rs376919970 | in-del | -/TCCC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937738 | GTGGTGTGTCCTCCC[-/TCCC]ACAGTAGACTTGATG | 26259 |
rs376942403 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000096 | TCGCCATTCTCCTGC[C/T]TCAGCCTCCCGAGTA | 26259 |
rs376985218 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030606 | TAAAGATAACGGAGT[A/G]TAAAGTCATTAGACC | 26259 |
rs377007272 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116958289 | AATACTCTTGCTTTT[A/G]TTGATTGGTATTCTT | 26259 |
rs377011737 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116997382 | GGGGAAAGTTCCTTT[C/T]AGCTATAGTCAAGAT | 26259 |
rs377015638 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932604 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAACCT | 26259 |
rs377021760 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116972776 | TTATGGTGTTAAATA[C/T]AGATAGAGAAGTAAA | 26259 |
rs377042793 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996578 | TTGCTTTGTGAACTT[C/T]CCATTTAAAAATTTT | 26259 |
rs377051752 | in-del | -/ATC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013240 | GAGCGAGACTCCATC[-/ATC]TCAAAAAATAAAGAA | 26259 |
rs377090896 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980004 | GTTAGTCTTTTGGCC[C/T]CAGCTAATTGGATGA | 26259 |
rs377094662 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116916143 | TGATAGCCAGTTTGG[A/G]ACTCTCAGATATAGT | 26259 |
rs377098678 | in-del | -/CTTA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026643 | TCCTCCCAGCACTTA[-/CTTA]ACTCTGGGTCACACA | 26259 |
rs377176624 | snp | G/T | 1.79519e-05 | 0.00299593 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985192 | TGTTACCTGCATTGT[G/T]TCTTGCTGCATAGGG | 26259 |
rs377224577 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117015380 | GCAGTGGGCTTACTC[C/T]GTTCTGGCCAGAATC | 26259 |
rs377300123 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968574 | ACAGTGTTGTAGTGA[A/G]AAACCTTGTAAAGAT | 26259 |
rs377376468 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962188 | GTGTGAGTGGACCAA[A/C]CTCCTCTGTGGGAGA | 26259 |
rs377394680 | in-del | -/TTGT | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967647 | TTCTTTCTCTGCAAA[-/TTGT]TTGTTCCTGTCTTTC | 26259 |
rs377396777 | snp | A/T | 3.36101e-05 | 0.00409926 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985215 | GCATAGGGTTTCTTA[A/T]TATTTGGGATTTAAG | 26259 |
rs377397669 | snp | A/G | 0.021333 | 0.101051 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951373 | ATCCCTTTTCATTTG[A/G]GACAGCGGTGTTTGT | 26259 |
rs377401941 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116923115 | GGAGGCTGAGGCATG[A/C]GAATCGCTTGAACCT | 26259 |
rs377440312 | snp | A/C | 1.66868e-05 | 0.00288845 | intron-variant | FBXW8 | GRCh38.p7 | 12:117028006 | CAGCCCTGACCTGTC[A/C]CCATCTTTGTGCTCT | 26259 |
rs377453140 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912257 | TACTGTTGCTCTCCC[A/G]GCCCACTGCAGCCTC | 26259 |
rs377454723 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010352 | CCTGGAAGCAGGACG[C/T]CGCCTCTTGAAGCTG | 26259 |
rs377532127 | snp | A/G | 1.65015e-05 | 0.00287237 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945397 | GTGATTGCAGAGGAT[A/G]AGGTGCTGTGGTACA | 26259 |
rs377536846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116976782 | AAAATGTCAACATTT[A/G]CAAACATGCCAGATG | 26259 |
rs377547151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931357 | AAAACACTGCAAATA[A/G]CCAAAGCAATCCTGA | 26259 |
rs377589416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952760 | TTTATTGTTTTGAGA[C/T]ACAGTCTCACTCTGT | 26259 |
rs377641661 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928796 | ATTCAGGAAGTCTGC[A/G]GTGGGGCCTGACAGT | 26259 |
rs377730206 | snp | C/G | 1.64827e-05 | 0.00287073 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010457 | GGACGGGAGGTACGT[C/G]AGTTGGAAGGGCATT | 26259 |
rs377731562 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946452 | TAATTCGTTTTGTGC[A/G]GGGCTGTCCTGTGCA | 26259 |
rs377743126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968151 | TTAATCTAAAAGTGA[A/G]TGGGGTTATTTTGTA | 26259 |
rs386766729 | in-del | AGGGAGG/TCATTATGTACGCACTA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012191 | TATGTACGCACTGCC[AGGGAGG/TCATTATGTACGCACTA]TGTTCCATGCATAGT | 26259 |
rs397716833 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913182 | GGTATGATCAGGCAA[-/A]GTTTAAGACATTATA | 26259 |
rs397759618 | in-del | -/C | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998723 | TGTTTGCCTTTGTTC[-/C]AGAGGTGAAAACACG | 26259 |
rs397782247 | in-del | -/T | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940506 | GCTTTTTTTTTTTTT[-/T]CCTTCCAGTTTGTGT | 26259 |
rs397804024 | in-del | -/T | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937865 | AGCTTTTTTTTTTTT[-/T]AATGCTGCAATTCAC | 26259 |
rs397809834 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996522 | AGAACAAAAAAAAAA[-/A]CTTGGTATTTTACAA | 26259 |
rs397818934 | in-del | -/T | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942390 | TTTTTTTTTTTTTTT[-/T]CCGAGACAGAGTCTT | 26259 |
rs397937910 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950193 | ATTGTTTTTTTTTTT[-/T]CTCCATGGCCAACAC | 26259 |
rs397946872 | in-del | -/TTTTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011142 | TTTTTTTTTTTTTTT[-/TTTTT]GGCCAGTTATCTGCT | 26259 |
rs397954344 | in-del | -/A/AG | 0.00597247 | 0.0543191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971371 | CAAAAAAAAAAAAAA[-/A/AG]GGCAGAATTCTGAAC | 26259 |
rs397967524 | in-del | -/AAAA | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979796 | AAAAAAAAAAAAAAA[-/AAAA]CACTTGCTTCTTATG | 26259 |
rs398021233 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918004 | TCAAAAAAAAAAAAA[-/A]CAAAAAAAAAACAAC | 26259 |
rs398021235 | in-del | -/AGAAAA | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947754 | AAAAAAAAAAAAAAA[-/AGAAAA]GAAAAGAAAGAAAGA | 26259 |
rs398021236 | in-del | -/G | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955048 | AATGGGGGGGGGGGG[-/G]CCCTGTATTAAGCAT | 26259 |
rs398021237 | in-del | -/T | 0 | 0 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981627 | TCTTTTTTTTTTTTT[-/T]AATTGAGACAGAGTC | 26259 |
rs398021238 | in-del | -/T | 0 | 0 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982640 | TTTTTTTTTTTTTTT[-/T]CCCAAAAAGACTCTT | 26259 |
rs398055967 | in-del | -/TA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936036 | AGCTTCCATTGTATA[-/TA]CAATAAAGACATGAT | 26259 |
rs527245938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962074 | CCTTCTGTACCAGTG[A/C]CCTGGGACTGATGAT | 26259 |
rs527257307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970456 | TGCCCTGGGCGGAGG[C/T]GACTATGATTTCTCA | 26259 |
rs527267811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012137 | CTGACTGTATACACT[C/T]AGTAAAGCTGACTTT | 26259 |
rs527274265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934915 | GTGCTACTCTTTCAC[A/G]GTCTTTGACGGCCAC | 26259 |
rs527277898 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019219 | TAGCAACGGACCTAT[G/T]ATGTATCATCTATAC | 26259 |
rs527376599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913396 | TTTTGACTCTCCCAA[A/G]ACTTAACTACGAATA | 26259 |
rs527396109 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962594 | ATACAGTTTCCTAGT[C/T]TATGTACTTCTTTTT | 26259 |
rs527414645 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912322 | CATCCCGCGTAGCTG[A/G]GACTACACGCATGCG | 26259 |
rs527420626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012643 | ATTAGAGATGCTGGC[C/T]CAGGCTTGTATAGCT | 26259 |
rs527423217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912763 | CCACCGCGCCCGGCC[A/G]AGAATAATTCTTTTA | 26259 |
rs527468214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955831 | TATAAAACCTGAGGT[A/G]CAGGGCTAGGTGTCG | 26259 |
rs527471796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947974 | GGCCTCTGCACACAG[A/G]TGCAGGGTTCTGTGC | 26259 |
rs527483287 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000501 | ACACTGAGCACTGGC[C/G]CCACCCCCGGAGCTT | 26259 |
rs527531521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955177 | CTGGACTTCCATTAC[C/G]TCCGTGAGCGCCTTC | 26259 |
rs527551690 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941677 | AACTGAGTTCTTAGA[G/T]TCCCACTAATTTTAC | 26259 |
rs527555994 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030183 | GCTTAAGATACGCAG[C/T]CATTCCATATTCATC | 26259 |
rs527567622 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994100 | AGAGGCATCCCATTA[C/T]CTGACTTCAAATTAT | 26259 |
rs527610368 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116993250 | CTGGGATTACAGGCA[C/T]GTGCCACCACGCCTG | 26259 |
rs527681000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005108 | TGGCATCTGAATAGT[A/G]TGAAGAGATCTCTGT | 26259 |
rs527710069 | in-del | -/TA | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029811 | GACGGGGGATATTGC[-/TA]TGTTGGCCAGGCTGG | 26259 |
rs527734230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961142 | GTGGGATTACAGGCA[C/T]GCACCACCACACCTG | 26259 |
rs527739061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947279 | TGAGTGAACTGGAGC[G/T]GACTGCAGGCTGAAC | 26259 |
rs527764267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999713 | CCTTCTAGACTGTGG[A/G]GAGTCAGGCCCCATC | 26259 |
rs527767323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991708 | ACAGAGCATTTGGTT[C/T]ATATTTGTTTGTACC | 26259 |
rs527809543 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946728 | TACGGTAATAAACTC[A/G]TCTGGAGGGAGCCCC | 26259 |
rs527824903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999117 | AAGCATTCCCTCGAT[A/G]TGTTATTAATTTACA | 26259 |
rs527866309 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989588 | TTTGAGTGATGACTA[A/C]ATTTTATCACTCCCT | 26259 |
rs527878034 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028939 | CATTGCCTTACTCTT[C/G]ATTTTCAACAGTTCT | 26259 |
rs527897409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992358 | CAGTGTTATGGGCCA[C/T]GTAAAGTCATAGAAA | 26259 |
rs527915331 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028370 | CGTGTGCCAGGGCTC[A/G]AGTCCCACGTGCTGC | 26259 |
rs527923910 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986028 | TTGTAGAGTGGGAGA[C/T]GATTTGGTGTTAAGA | 26259 |
rs527946678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926730 | AGAGAGCTGTCAGCT[C/G]TTACTCTTTTTTTCC | 26259 |
rs527952599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025195 | CAGCACCACTGTGAA[A/G]AGACATTCGGCCAGA | 26259 |
rs527977627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977022 | CGAGAGCCCCACCCC[A/G]GACATCGGGGCCTTG | 26259 |
rs528004938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933141 | TTCTAACTTTACACA[G/T]TGGCCTGCTCCCAAG | 26259 |
rs528077823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002360 | ACATGAAAGCGGCTC[A/G]GGCTGCTTCTCCCTT | 26259 |
rs528116560 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116957342 | CAGCGAGACTGTCTC[-/A]AAAAAAATTTTTTTT | 26259 |
rs528135549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936329 | CAAGTGGGTGGTTGT[C/T]GTACGCTGAATAATG | 26259 |
rs528155447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944110 | TAAGGCAATCCTGGA[A/G]CTGGAAGAGGAAACA | 26259 |
rs528193354 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025482 | GAGAACACAACCTCT[C/G]AGCAGCGACATGGTC | 26259 |
rs528193458 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001158 | TTTGTTTATGTGCAA[A/C]ATGCTGCTAAGCATG | 26259 |
rs528268825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929246 | TTGATTTTTCTTTTC[G/T]TTTTTTGAGACAGAG | 26259 |
rs528345399 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950434 | TAGTTTGGATCAGCT[A/G]TGGAGTGAGACGCCT | 26259 |
rs528348450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015310 | CCAGAGTCCTCAGGT[A/G]TTTGTTTTTGTGTTT | 26259 |
rs528362046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923992 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 26259 |
rs528371333 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970303 | TGGTGCATATTAGCA[C/T]GAGGAAGCCTGGACG | 26259 |
rs528386561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973993 | ACATTGGAAAATAAG[C/T]AGCCCATGGCTGTGA | 26259 |
rs528419514 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929679 | ACATGTATTACCTCA[C/T]ATACTTATTTTCTGT | 26259 |
rs528424584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979184 | AGCACTTTCCAGATA[C/T]CGAGTAATCTTTACA | 26259 |
rs528442831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987097 | TATACGCCCCTGAAT[A/G]GCAGTGGCAGTGTTC | 26259 |
rs528455397 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998887 | ATTTAAAACATTTTA[A/C]TGTTTTCAAAATACA | 26259 |
rs528468564 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966430 | CAGAGGTGCAAAGAA[A/G]CCAGGTAGGTTGAAG | 26259 |
rs528471043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025722 | GCACTGAATTGCCAC[C/T]AGGTGGTGCCAAACG | 26259 |
rs528473667 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934444 | TATGTTCATCTTTTT[A/T]TGTGCCCACAGGATT | 26259 |
rs528495975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986357 | GTACATTTCTGTTCT[A/C]AAAACTTCCATAGTA | 26259 |
rs528557312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928523 | TGAGGGGGTCAGCAC[A/G]AGGACAGAACATGTT | 26259 |
rs528567662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922186 | TTCGAGACAAATTGT[A/G]GATTATAAATGGATG | 26259 |
rs528584350 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938231 | AAGCACCCTCCTTTT[A/T]TAGTTTGCTAAAGAA | 26259 |
rs528597369 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968818 | GAGAAAGGTTAAATT[-/A]AAAAAAAAAATGTGT | 26259 |
rs528601292 | in-del | -/CACTGC | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942448 | GGCGTGATCTTGGCT[-/CACTGC]CACCTCTGCCTCCTG | 26259 |
rs528620789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935343 | CTAAAATCCAGGTGC[C/T]TATAGCTAAAGATCT | 26259 |
rs528709483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938914 | ATGGAGAAGTAGCCC[C/T]AGTCTGGGTGCATCC | 26259 |
rs528746630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008891 | GGATCACTTGAGGTC[A/G]GGAGATCGAGACCAG | 26259 |
rs528746940 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010608 | CTCAGAGAACAAAGT[C/T]CTGTATTAGGTAATA | 26259 |
rs528767807 | snp | C/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909011 | GACAATTCTGAGCTG[C/T]GTTCTAAGGCTCCTT | 26259 |
rs528775544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116916479 | GTCAGGGTAATAACC[A/G]CTGCCCCCATTAGCT | 26259 |
rs528785173 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965756 | AGGGCTGAGATCTTA[A/C]ATACATACCTATATA | 26259 |
rs528792286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956842 | GCATGGTGACACGTG[C/T]CTGTAATCCCAACTA | 26259 |
rs528808793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007882 | CTCGTAACGTGGAAA[G/T]AACTGCCTTTGAGAT | 26259 |
rs528813651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975560 | ATGAGTAACAGGACA[C/T]TTGCATGGTGTGAAA | 26259 |
rs528826959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915518 | CCAGCATGTCAGAAC[A/C]ACCTCCCCTGCCCTG | 26259 |
rs528872145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023828 | GGGCAGTACACCTAC[C/T]GCTGGGACAGGCGTC | 26259 |
rs528875674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931620 | AAGTATTTATTTTTG[A/G]TGTGGCTATTGTGAA | 26259 |
rs528899717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983359 | TGCTGTGGAACCTTT[C/T]GTGATCCGCTTATCC | 26259 |
rs528948282 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933669 | CAGAACCCCGTTAGC[A/G]TACAGTGACTAAGTT | 26259 |
rs529022936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969717 | CTACACGCACATTCT[C/T]GGTGGAGGGAATCGT | 26259 |
rs529056919 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000925 | TGACACGAGCTGCGC[C/T]CCACCTAGTGCCACC | 26259 |
rs529082441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969088 | TTCAGTTGGTCTGTC[C/T]GGCAGCTTAAATTTA | 26259 |
rs529115412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018280 | TACAATTACAGCTTT[C/T]AGACCAATTATTTTT | 26259 |
rs529138137 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999335 | GGAGAACTGTGCCAG[A/G]GACGTGGGATGACCG | 26259 |
rs529161520 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944639 | GTCCATCTTTTGCAG[C/T]CTGGCCAACTTTGCA | 26259 |
rs529194231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953519 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 26259 |
rs529209744 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925077 | TCTATCACTTTGGTT[-/A]AAAAAAAAAAAGATT | 26259 |
rs529227116 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116972627 | GCATACAGGGAGACT[A/G]AGGAGGTAAGTATGT | 26259 |
rs529258805 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984431 | AGAGTGGAAAATCGG[C/T]ATTTTTGGCAAGTGT | 26259 |
rs529270716 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967731 | GAAATAATCCTTGCC[A/T]TATGTGTTTCCGATA | 26259 |
rs529282607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009828 | TTTATAGTTCAGTCC[A/G]AAGGAAGCATCCAGT | 26259 |
rs529309483 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965775 | CATACCTATATATAT[C/T]TGAGACAGGGTCTCA | 26259 |
rs529334250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116974717 | GCCATTGCACTCCAG[C/T]CTGGGTGACAGAGTG | 26259 |
rs529334356 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966881 | CCACCACAACAACCA[A/G]CTAATTTTTGTATTT | 26259 |
rs529356370 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941655 | GTCAGATTTTGACAC[C/T]AAGATAAACTGAGTT | 26259 |
rs529381852 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995609 | AGCTGTATGTAGGAA[A/G]AAGGGCTGCTTGATG | 26259 |
rs529437056 | snp | A/G | 9.88403e-05 | 0.00702925 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010407 | TGTGTCAACCTCAGC[A/G]ACAGCCCTCCCAACC | 26259 |
rs529482478 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910650 | CTTAAACGCATGCTC[C/G]AAGACGTCAGAGTTT | 26259 |
rs529507134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938639 | GTTTCCATTTTAAAG[C/T]GGTTGAGATTTGCAC | 26259 |
rs529535312 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004129 | TTCCGCCCAATTCCT[C/T]AACTCGGTATTCCAG | 26259 |
rs529555369 | snp | C/T | 3.40223e-05 | 0.00412432 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027986 | TGGGGTGAGGGCCAG[C/T]GAGGCAGCCCTGACC | 26259 |
rs529569594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990453 | AACTTTCTTTTCCCA[G/T]CCCTGGTGAGCTCAT | 26259 |
rs529586863 | in-del | -/AACCGCGG | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919132 | TGCTATGGAAAGCAA[-/AACCGCGG]AACCGCGGATAAGGG | 26259 |
rs529650976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013344 | GTATGCTTTTCCCTC[A/G]CTGGGAGGGAAGGCT | 26259 |
rs529654005 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998164 | TGGTAGAATGGGACA[C/G]GTCAATTTAGCTTCC | 26259 |
rs529679880 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000923 | AATGACACGAGCTGC[A/C/G]CTCCACCTAGTGCCA | 26259 |
rs529700592 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006519 | CCCGCCTGCCCACGG[C/T]GGTGGCTGATGCCTC | 26259 |
rs529758806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955886 | CCACCTAGTGAAGAG[C/T]GCATCTCAGGTAGAA | 26259 |
rs529759341 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950858 | CAGCTCCTTTCTACC[A/C]ACGGATGCTACAGTT | 26259 |
rs529760098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962889 | TTGAGGGCAGTGAGC[C/T]CCAGGGTATGTGTTC | 26259 |
rs529762586 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960317 | TGTGGCTTTCACTTA[C/G]GTTAGATTTGAGAGC | 26259 |
rs529780462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007776 | CACTAGTCTATGGCA[A/G]TCAGATAAAATGAAG | 26259 |
rs529838778 | in-del | -/TGCTTA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927286 | TACCTCATCTCTAAT[-/TGCTTA]TGCTTATCCAAAGGC | 26259 |
rs529877603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994922 | CCATGATTTTGATAG[A/G]CATTGCCCTCCACAG | 26259 |
rs529892615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948907 | CTACAGGTGCATGCC[A/G]CCACACCTGACTGTC | 26259 |
rs529897157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935554 | CTCAAGACCCAAGTG[A/C]CCTCAGGAGTTCCTT | 26259 |
rs529908885 | snp | A/G | | | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032639 | TAACCCAAGCCATGT[A/G]CCACCCTGGTGCTGC | 26259 |
rs529915069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026458 | GTCCCATGCCAGGTC[C/T]ACCAACACTTTCCTT | 26259 |
rs529924341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001701 | CTCTCTGTGGGGATG[A/C]GGCCTGTTGGGAGCA | 26259 |
rs529949316 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030702 | AGAGCCTGTTTCTAA[A/C]GTACCTGCCATTCGT | 26259 |
rs529995551 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011472 | AAGGCCTCCTAAAAT[A/G]GCTGATGTTCCGGTG | 26259 |
rs530041827 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116999189 | CAGCCCACATCTGAG[C/T]GGTCGCATCCCAAAC | 26259 |
rs530100707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024794 | TCATGTGTAACCATG[A/G]TTCTGCCCGTTGCTT | 26259 |
rs530105792 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029439 | CTGACAGTAAAAGCA[C/T]AGAATACAAAACCCA | 26259 |
rs530114482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947113 | CTGGAGGTGGCAGAA[C/G]TGACGATATTTTAAA | 26259 |
rs530121936 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979940 | TTGTCTCCTTGCCCT[A/G]AGGTCCCTCCCCAGG | 26259 |
rs530163962 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946773 | CGTGTGCCTGGGTAG[A/G]TCCATGTGATGCACA | 26259 |
rs530174871 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940756 | GGACCATTAGTTGAG[G/T]AGCCATGTTGATGGC | 26259 |
rs530204364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977782 | CTTTGCCTTCTCCAT[C/G]AATCTGTTTTTCCTA | 26259 |
rs530218146 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029042 | TAAAATCCATTCTCA[C/T]GGCAGGCAAATCAGT | 26259 |
rs530237178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940181 | CTGCTTAATGGATCC[A/G]TGTCAGCCTGGGGGG | 26259 |
rs530238997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947798 | GTTGGGGCAAGTTGC[G/T]TTACTTTTGTCTGCC | 26259 |
rs530387241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997307 | TATTACAGAAGCCAT[A/G]ATCTTTAGGATCTCT | 26259 |
rs530388458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927725 | TGTGCCGTATACCAG[A/G]CTGGAAGATAGCACC | 26259 |
rs530413296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978709 | AAGACCAGCTCTGTA[A/G]TTGAAGAAGGGACTA | 26259 |
rs530425025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970528 | AGCTGCTTTTTAGCG[C/G]TGAACAGTAGGACCA | 26259 |
rs530443925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996464 | CCCATACCTCCACCC[A/G]AACAGGAAATCCATC | 26259 |
rs530464019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025625 | ACATTTTATCAGACA[A/G]AGCCCTGGGTACTGC | 26259 |
rs530515182 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989729 | TTGGGTTTTTTCCCA[A/G]TTTCCCTGCTCCTGA | 26259 |
rs530515460 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032030 | AAAATTGTCAGGAGC[A/G]CCTCCTTCCACCACG | 26259 |
rs530518929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944261 | AGTTGATCGATCATT[C/T]TTGGTGGAATTCTTA | 26259 |
rs530519806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981857 | GACCTCAAGTGATAC[A/G]CCCACCGCAGCCTCC | 26259 |
rs530533726 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975513 | TTTAACACTGAAATG[A/G]TGGTAGGGGGGACAC | 26259 |
rs530596196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027648 | ATTGGAAACATAAAC[A/G]TGGATGCTGACCTGT | 26259 |
rs530607369 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950646 | AAAAAAAGTATTTCT[A/G]CTTTAAACAAGATGT | 26259 |
rs530626921 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032460 | TTTTTCTCAATGTTA[C/T]AACAAAATGACATTG | 26259 |
rs530636223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015792 | ACAGTCCATTTTAGA[A/G]CATTTTCACCCCAAA | 26259 |
rs530686185 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016646 | CTATTTGTCTGGTTT[G/T]TTTTTTTTTTTCCTT | 26259 |
rs530712190 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116999373 | CCAAACTGAATTCCT[C/G]ATCCAGATTTCTTTG | 26259 |
rs530722028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930856 | TCTGTTGCCCAGGCT[A/G]GCATGCAGTGGTACA | 26259 |
rs530756080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023530 | AAGTAGTTTTTAAAG[A/G]GGTTCTTAAAGAAAT | 26259 |
rs530808345 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918292 | TGTGCTGCTTTCTTC[A/T]GTGGAGTGGCTGTGA | 26259 |
rs530842091 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979903 | TGCAGGAGAGAAGTC[A/G]TAGAGATCTTTGGGC | 26259 |
rs530872395 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921277 | TTCACTTATATCACC[C/T]GCACATGTGATCAAC | 26259 |
rs530906006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980737 | CAAGTTAAAACATCT[A/G]GAAAAGTTTGCTGCT | 26259 |
rs530908276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020714 | CCTTCAGTGTGTTTG[A/C]TGAAACCACGGAGCT | 26259 |
rs530912297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026831 | GACCACAGCCGGTAC[G/T]GCATGAAAGTTTCAG | 26259 |
rs530960856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987646 | ACACAAATGTTAAAA[A/T]TTTTTTTGCGAATTT | 26259 |
rs530990543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957775 | GGAACTCGATCATTA[C/T]CCGTTAGGGACCTCT | 26259 |
rs530990799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966609 | TACAGCTTGAGGTGA[C/T]GTGCAGGGGTGCTGC | 26259 |
rs530997332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014700 | TTCCAAAGCTGTTCA[A/G]TTTCTATGCTGTTTT | 26259 |
rs531020464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008939 | AGGTGTGGTGGCGGG[C/T]GCCTGTAGTCCCACC | 26259 |
rs531041760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972894 | AGCTGTTGAAAGTAT[C/T]ACTATCTACTAAAAG | 26259 |
rs531055534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965903 | AGCTGGGACTACAGG[C/T]GCATGCCACCATGCC | 26259 |
rs531068795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021292 | TTTTTCTTATCTTTT[A/C]TGTCGATTTAATAAT | 26259 |
rs531127889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950886 | GTTTGGTGTGAACTC[C/T]GGAAGGTACTTAGAT | 26259 |
rs531138467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116916522 | GTAGGAATGTGGTCC[C/T]AGTGTTGTAAGGTCT | 26259 |
rs531153355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002395 | CTGAATTTGAGCATG[A/G]ACGGTGCCAGAAGCA | 26259 |
rs531189685 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951503 | TTTCTCTTGTACTTA[A/C]CTCGTGTTTCTCTTA | 26259 |
rs531209535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932948 | CTTAAGTGGGGGCAT[C/T]GGCAGATATTTTTTG | 26259 |
rs531212288 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116974537 | TTCTGAGTGTCTTAA[C/T]TTTGCATCAGAATAA | 26259 |
rs531276349 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950162 | TAGTACCTATTTGTT[A/T]CTTAAGTTGTCCTGA | 26259 |
rs531314929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017789 | GAGCCAGACACTGAA[G/T]AGGCTTCAGCTTGCC | 26259 |
rs531317707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969821 | GTAGGAACACTGTAC[A/G]TGCACCTGGGGTGTT | 26259 |
rs531326494 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946175 | GAGGCTGGAGATTCA[A/G]TGGTAGAGAAGGGAT | 26259 |
rs531340600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925993 | TACTGGTGGCAGGGC[C/T]AGGGTGATGCCAAGA | 26259 |
rs531372349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976357 | ATTTGTCTTCAAGCT[A/G]TTCCCCACCTGCACC | 26259 |
rs531387590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962557 | AGCAGGAAGCAGAAG[A/G]ACAGAGACTGGCAAG | 26259 |
rs531395154 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116989155 | TTGTATACTAAAAAC[A/G]TATTGTTGTAGAGAT | 26259 |
rs531402754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011973 | ATTGTATTCGCTCTT[A/G]TAAGTAATCTAGAGA | 26259 |
rs531463241 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932320 | ATACTGCATTTTACA[C/T]AGGTGTTTACAGCTT | 26259 |
rs531477877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018435 | CTGTTTCCCAGCGTC[A/G]AGTATTTGGTTTGAG | 26259 |
rs531509685 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013892 | AAAAGTCTGCAGGAA[A/G]TAATCACTTGTTTTT | 26259 |
rs531542472 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012542 | TTGCACATCTAGAAA[A/C]AAGGAATGAGGAAGC | 26259 |
rs531603881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010948 | TCTATTTAGCTGATT[A/T]GCAGCCTTCTCTTTA | 26259 |
rs531609916 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910210 | CACTGAACCCAAGTT[A/G]TAGTCTTTTATCCCT | 26259 |
rs531682297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006385 | GGGTGAAGGAAGAAG[C/T]TGGTCTGCCTTGAGC | 26259 |
rs531688048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913303 | ATAGTAAAGAAGCAA[A/G]TCATGTACAGTTGAC | 26259 |
rs531713610 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029661 | CTAGACTAGACTGGA[A/G]TGCAATGGCCTGATC | 26259 |
rs531780783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959732 | AAATCATTTTAAATT[A/G]TCAATCCCTCTGTCG | 26259 |
rs531782169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938765 | TTCAGAGGCTCCATC[C/T]AACAAAACGAAGCTT | 26259 |
rs531787745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946215 | CTCTTTACTCCCATA[A/G]AGGTCAATCCTAATA | 26259 |
rs531815926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998243 | AAACCCTTCAAGATG[C/T]GAAGCCTTATTGGAG | 26259 |
rs531848416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952927 | ATTTTTAGTAGAGAT[C/G]GGGTTTCACCATGTT | 26259 |
rs531849336 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009254 | TATCATCAGCAGGCC[A/G]TGGTGTTACACACAC | 26259 |
rs531902409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991572 | CGTGTGTCCCAGCAC[A/G]TTTTATTAGGCTGGT | 26259 |
rs531927651 | snp | A/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983144 | AGTTTTTTTTCTCTT[A/T]ACTGTTGTGATGTCT | 26259 |
rs532001489 | snp | A/C | 0.000214195 | 0.0103466 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024198 | CCTGTCGCTCTCCGC[A/C]CATCAGCTCAGGGTC | 26259 |
rs532004613 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955716 | AAACATCCCTGTTCT[A/G]TTTTGTGATGCTTAG | 26259 |
rs532041243 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028287 | GAAGAAAGCAGCCCA[A/G]GGTGCCATGCCTGAC | 26259 |
rs532044893 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929297 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTTCCTG | 26259 |
rs532069255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985111 | TTCCAAGGTATCTCC[A/G]TTAAAAAATTTTCCT | 26259 |
rs532088084 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995003 | GGTTCTTGGACGGCT[G/T]TTCTCTGATAGGCTT | 26259 |
rs532122454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956770 | GTCAGGAGTTTGAGA[A/C]CAGCCTGGCTAACAT | 26259 |
rs532171324 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950125 | GGGCTTTGGCCACAC[A/G]TAATCTTCCTTCCCC | 26259 |
rs532174766 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031366 | TAACTCTTCACCAAC[C/T]GTCATCAATAGGTTT | 26259 |
rs532183807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956182 | TAAATATTTTCTCCC[C/G]TGGTTTCCGCCTTTT | 26259 |
rs532210789 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030778 | TGTCATCTTCAAGCA[C/T]GCCAACTTCAGGCAG | 26259 |
rs532213121 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002272 | CTACCCAGCGCCTGG[C/T]GACGCTCAGCAACAC | 26259 |
rs532245274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027225 | GCTCACCTGAGCTTC[A/G]GGAACTGAGGTGAGA | 26259 |
rs532278343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021402 | ATCATTGGACTGACT[G/T]TCTGATTGTTCCCCC | 26259 |
rs532298506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987761 | ATTTTTTGAATTGCT[A/G]TTACATCCCCATGGT | 26259 |
rs532314846 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032177 | TTCCTTCTTTCATTT[C/T]CCAACTCAGTTATTC | 26259 |
rs532352637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995822 | CATGCTGTGGTGCAA[A/T]AGTCAGTGTGAACGC | 26259 |
rs532361314 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987212 | CCCCCGGATGTTGAC[A/G]CTCCCTCCAGCTCTT | 26259 |
rs532386106 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973303 | ATAATTGATTCAGAC[-/A]AAAAAATCAATTGAG | 26259 |
rs532424629 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030568 | TTTTGCAGGCGCATT[C/T]GCCCTTCCTAGTTTG | 26259 |
rs532438290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980914 | TATGAAAACAGGTAT[C/T]CTTTCAATTCTTATA | 26259 |
rs532462336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936224 | CTCTGGCAGAGTGGA[A/G]TAGCAAGGACGAAGG | 26259 |
rs532463416 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029172 | AAAACCACCCTGTAC[A/G]AAGGCCACAAAGAAC | 26259 |
rs532470841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025679 | TGTGCCTGTTGAGGG[C/T]GCCTCGGCCCTTTTT | 26259 |
rs532545729 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029566 | ATAAAAACAGACATC[A/G]GTGGAATCGAAAACC | 26259 |
rs532566461 | snp | A/C | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916610 | TCTGCATGAGAAAAC[A/C]ATCCAAGCTGGGCAT | 26259 |
rs532602079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978950 | TTTAGTTGGGACTTA[C/T]CTTTTTGATGGAAGC | 26259 |
rs532614243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927277 | TAAAGCCCGTTACCT[C/T]ATCTCTAATTGCTTA | 26259 |
rs532618522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934327 | TCTCTCTGTGGGAGT[A/G]TTTCTTGCCGAAACA | 26259 |
rs532624135 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013177 | AACCCAGGAGGCGGA[A/G]GTTGCAGTGAGCTGA | 26259 |
rs532684627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933816 | AGTAATAAAAATAAG[G/T]AGCACTTTCATTTGT | 26259 |
rs532718272 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982644 | TTTTTTTTTTTTCCC[A/T]AAAAGACTCTTCTCA | 26259 |
rs532737329 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117005695 | GCACTATGTGCCAAG[A/G]ACATCATGGAGAAGA | 26259 |
rs532748358 | in-del | -/TCC | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015402 | GCCAGAATCAGAACG[-/TCC]TCCTTTCTTTTCAGT | 26259 |
rs532754258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927957 | TGGTCATTTAAAGGG[C/T]CTGTAAATTTGAGTT | 26259 |
rs532775547 | in-del | -/T | 0.0032428 | 0.0401358 | intron-variant | FBXW8 | GRCh38.p7 | 12:116918966 | CCTGTATATGCCATG[-/T]TTTTTTTTCCTATAT | 26259 |
rs532818740 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922657 | ATTAGTCTTACATTA[A/G]CACATAGGAATACAA | 26259 |
rs532851192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972030 | CTAGTGAAAGTAAAT[G/T]GAAATATTTTTTCTC | 26259 |
rs532854734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983280 | CACTGGCATTTTCTG[A/C]AGCATATTTTTCTCT | 26259 |
rs532866842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963827 | GTGTGGTTCTATCAT[A/G]AGGCCCTTAAAGGCA | 26259 |
rs532876839 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008449 | GTTGAAATGTTCTGC[A/G]TCAGAAATTTTTCTT | 26259 |
rs532896254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023162 | ACTTGGAAAATTGAC[A/G]TGTGTGCGCATGCTT | 26259 |
rs532931875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937592 | GAGAAATGACCATTG[A/G]GTTTTGCAAGTTGGA | 26259 |
rs532956186 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032980 | ACGGCTTCCCCTGGT[A/G]AGGGTCCAGCCTTCT | 26259 |
rs532957433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989862 | TCCTCATTTGTAAAA[C/T]AGAGTTCATAATAGT | 26259 |
rs532958006 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027704 | GACAGCCCCGTGGGG[A/C]GAGTCCACGCTGTCG | 26259 |
rs532967061 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020739 | GGAGCTGAGCCTGGC[A/G]CTTGCCAGCAGCCTC | 26259 |
rs532985760 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975537 | GGGACACAACATTCA[A/G]ATGAGCAATGAGTAA | 26259 |
rs533018574 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023795 | AGGTTATTTTACCAA[C/G]AGCAAAATTACTGTG | 26259 |
rs533027565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931495 | GATAATATTCTTCCA[A/G]TCCATGAACATGGAA | 26259 |
rs533056392 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919837 | GTTTTAATACTGCTG[G/T]CCAATATTTATCACT | 26259 |
rs533071299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027943 | TATCTGGTCTCAGGC[A/G]AACGCCTCCTGCACA | 26259 |
rs533076850 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968819 | GAGAAAGGTTAAATT[A/T]AAAAAAAAATGTGTA | 26259 |
rs533089884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930932 | CCCACCTCAACCTCC[C/T]GAGTAGCTGGGACTA | 26259 |
rs533123070 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017461 | GCATTAAACTGGCAG[G/T]TCTACCTGAAAATAC | 26259 |
rs533141264 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944708 | ATTAGTGTTGGAAAA[A/C]AAAATGCTAATAGTT | 26259 |
rs533178684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923488 | GCCAGTCTCACATTG[C/T]TGAGAGCTATTCAAC | 26259 |
rs533198661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973081 | ACTGGCCAAACCTGG[A/G]ACAACTGGAGTATCA | 26259 |
rs533212362 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018971 | AAAGTACTTGGTAAA[C/T]ACTTCCGCTCCCCCT | 26259 |
rs533213448 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992502 | ATGGATGAACTGTAT[A/G]GTGGGGAAGCTTGTG | 26259 |
rs533298663 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919055 | AAAATAGAACAATTA[C/G]AACAGTATACTATAA | 26259 |
rs533326918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959250 | TTAGGGTCAGGGGCT[A/G]TGTCCTGCAAACCTG | 26259 |
rs533344567 | in-del | -/T | 0.0277082 | 0.114396 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922812 | GTGTGTGTGTGTGTG[-/T]TTTTTTTTCCCTTGA | 26259 |
rs533400802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981649 | GACAGAGTCTCACTC[C/T]GTCACCCAGGCTGGA | 26259 |
rs533424387 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937443 | GCCAGGCAGAGGACC[A/G]GGAAGGAGTTCCCTG | 26259 |
rs533441781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917374 | GGAAGAGTTAGTTCC[A/G]TTTGAGACTCCCTAG | 26259 |
rs533480186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966789 | GCACCATCTCGGCTC[A/G]CTGCAACCTCTGCCT | 26259 |
rs533496644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015128 | AAAGATGGAGTTTCT[A/G]TTGGAGTTCTAGCTT | 26259 |
rs533499156 | snp | C/G | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996542 | GTATTTTACAAGCAG[C/G]ATGAAAATGAAATTA | 26259 |
rs533559028 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912377 | AATTTTTTGGTAGAG[A/G]CAAGGTCTCCCTGTA | 26259 |
rs533613353 | snp | C/G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116934336 | GGGAGTGTTTCTTGC[C/G/T]GAAACATCTTGAAAA | 26259 |
rs533652687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947076 | AAAGCAAGGGAAGAG[A/G]ACAGGTATGTCCTTG | 26259 |
rs533734725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940306 | CACAGACCATATTTT[A/G]CAGATGACTTATGGA | 26259 |
rs533750516 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992824 | TGTATCTACTCATTG[G/T]TTGATGGCACTTAGG | 26259 |
rs533785218 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947519 | TTGGGAGGCTGAGGC[A/G]GATGGATCACTTGAG | 26259 |
rs533863617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933330 | GAAATCATTTCTTTT[A/C]ACATTGCTTTTTGCT | 26259 |
rs533922653 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981463 | TATCTTTAAAAGATA[A/G]TTGCCTGCTTATGCA | 26259 |
rs533964163 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029162 | CGATGCACAAAAAAC[C/G]ACCCTGTACGAAGGC | 26259 |
rs533993797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023998 | CTGACAGTCTGTGCT[G/T]GATGTCCTTATTATC | 26259 |
rs534035982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926976 | AGCAGCCTTGCAATA[C/T]ATAAGACCGCTGTAT | 26259 |
rs534043409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939573 | TACATTTATATGATC[C/T]CTTGATTACTCTTGA | 26259 |
rs534053757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933915 | TTTATTTTAGAGGGG[C/T]TTGCTTTTTTTCTCT | 26259 |
rs534068203 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027203 | AGTCATGCCCAAAGC[A/G]TGGCCTGCTCACCTG | 26259 |
rs534073380 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985510 | ACTCAGAGCTTCCTG[A/C/T]GGGCCTTACCTCCAT | 26259 |
rs534083758 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029626 | TTTGTTTTTTTTCAG[A/G]TGGGGTCTCGCTCTG | 26259 |
rs534112291 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959888 | TTCACTGGGCTGGGG[A/C]ATATCCTCATTTGGA | 26259 |
rs534164824 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009575 | CGACAGTGACTGACA[C/T]ATAGGAAGCATTTAA | 26259 |
rs534170156 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946354 | CTGGGCAACCTCACA[C/T]GGTTTCTAGCAAAGT | 26259 |
rs534177986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011567 | AGGCTTGATAAGTGG[C/T]CCCACATGTGGCACG | 26259 |
rs534183900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938153 | TGTTGATTTTTTTTC[C/T]TTCAGAATTAAAAGT | 26259 |
rs534188428 | in-del | -/GGGGCTGGGAGGGGCTGG | 0.0126979 | 0.078662 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029460 | CAAAACCCAGGGGAT[-/GGGGCTGGGAGGGGCTGG]GGGGCTGGGAGGGGC | 26259 |
rs534203126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990127 | TAAATGGTCAAGAAT[A/G]GAAGCATCTTGGATC | 26259 |
rs534237552 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017885 | TGAGTTGTGACCCCC[A/C]AATTACAGAGTCTCA | 26259 |
rs534246191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945617 | AGCCTGAGATTAATT[A/G]CCAACAGCGAAGGGA | 26259 |
rs534265847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983567 | TGAATGATCCTTTAT[A/G]GTAAGATCCTAAACT | 26259 |
rs534306511 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951439 | GGCTTTCTACAGTTA[C/T]GTATCTCCAAGGAGC | 26259 |
rs534333340 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982997 | GCTTTGGACCAAGTT[C/G]TTTAACCGCTCGGTG | 26259 |
rs534357522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968548 | AGGACAGTTGTGTTG[C/T]GTTTGCCGTTACAGT | 26259 |
rs534375554 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928515 | TTGGTAGCTGAGGGG[G/T]TCAGCACGAGGACAG | 26259 |
rs534378751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017056 | CTCACCCTTTCTAAA[A/G]TAAGTAATGTAACAG | 26259 |
rs534389037 | in-del | -/AG | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006647 | TCGGTGGGTCTCCTC[-/AG]AGAGGCAGGCCCCGT | 26259 |
rs534439534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953500 | CAGCCGGCTGGGCGC[A/G]GTGGCTCACGCCTGT | 26259 |
rs534476620 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116911423 | AGGACAAACCCCTGC[A/G]GTGATTTGGAGAGTA | 26259 |
rs534495704 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917419 | GCTGATCCACTTGAC[A/G]TGAATGGGAAATAAA | 26259 |
rs534504417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923064 | TACAAAAATTAGCTA[G/T]ATGTGGTGATGTGTG | 26259 |
rs534515169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014435 | GGGTTGACATCTGTT[A/G]ATTGTCTTTTCCCTT | 26259 |
rs534518402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929594 | ACAAATAAAGTTATA[C/T]ATATGTATCAGGTAT | 26259 |
rs534547116 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011240 | CCTGGGCCCGGCCCC[A/G]GGCTGCAGGTGGCGG | 26259 |
rs534557064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979398 | ATGTCATCGTTAATG[A/G]CTGTTACTGGTCTAG | 26259 |
rs534614402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995211 | AGAAAGATCGGCAGC[A/G]TACGCGGACATGCTC | 26259 |
rs534633599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923529 | TTATTTTCTTTTTTT[G/T]TTTGTTTTGAGACAG | 26259 |
rs534633864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116916166 | GATATAGTGCCACCA[C/T]AAATGTTTTGTACAT | 26259 |
rs534659173 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116942529 | ACAGGTGCACGCCAC[C/G]ATGTCCAGCTAGTTT | 26259 |
rs534685505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980338 | CTCCATGAAGTAGCC[A/T]CATTCCTTTCCAGTC | 26259 |
rs534715496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978140 | AGCGCTGTGGTCAGC[C/G]GGAAAGCAGGATGGC | 26259 |
rs534723384 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939376 | CCCCTTCTTAGAGAT[A/G]TGCAGCACATGCCAC | 26259 |
rs534769063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006687 | GAGCAGGACAGCTGA[C/T]GGTCAGGCCCCAGCT | 26259 |
rs534803469 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920232 | AGCAGGCCTCCACTT[-/A]ACGAACCTTTTGAAA | 26259 |
rs534827231 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954012 | CTAGCTACTTGGGAG[G/T]CTGAGGCAGGAGAAT | 26259 |
rs534829927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972519 | TCATTCAAAAGGCCA[C/T]TAAACGGGCCCAAGT | 26259 |
rs534841883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013021 | CACTCAAGAAAAACC[A/G]GACGCTTGAGGTCAG | 26259 |
rs534891158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009094 | CAAAAACCTTTGGCT[A/G]GGTGCAGTGGCTCAG | 26259 |
rs534944492 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922257 | CCAACCAGTTTTTTT[-/C]TTCTCAAAGAAGACA | 26259 |
rs534994379 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019636 | TTTAATTATGAAACC[A/G]AACATATGTATGGGA | 26259 |
rs535013012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920991 | GTTTAGACTAAAAGG[A/G]GGCTCAAAGCAGAGG | 26259 |
rs535016924 | in-del | -/T/TTTTTT/TTTTTTTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011127 | GTTTTTTTCTTTTCC[-/T/TTTTTT/TTTTTTTT]TTTTTTTTTTTTTTT | 26259 |
rs535073978 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019254 | TCATCTGTGTCCACT[A/G]GATGGACTTGTTATG | 26259 |
rs535103492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924689 | GACATTCTGCTGCCC[A/G]ACAGTAGTAGGATTT | 26259 |
rs535112146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116974896 | ACCCAAAAGTAAGGA[C/T]GTTTAAAATAAATAA | 26259 |
rs535156625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921584 | GTGTAGACCATTTCT[G/T]ATATACTTGCTAACA | 26259 |
rs535228864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914731 | AAATACAAAATTAGC[C/T]AGGCATGGTGGTGGG | 26259 |
rs535229640 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117006810 | GATTGATAAATATCT[A/G]TTGGCCAGCTCTTGA | 26259 |
rs535250387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964160 | AGCACTGTCTGGCTG[A/C]TAAAGGCAAGATTTA | 26259 |
rs535275170 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997961 | GCTGGGACTACAGGC[A/G]TGTGCCACCATGCCT | 26259 |
rs535346019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949307 | GATACATGCCAGCCT[A/G]TTGTGGATGGTAGTT | 26259 |
rs535350450 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920095 | TGCCTTTTAAAGCTC[A/G]GCTTGAGTTCTGTCT | 26259 |
rs535353371 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971620 | TGTTATATCTGAATA[A/T]TGGGGCAGTGGGCCT | 26259 |
rs535426479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951071 | AGGGCAGGCCCCCTA[C/T]GAGTCCAGATGCCAG | 26259 |
rs535440136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016073 | CATTTTCTTTATATC[A/C]ATTAGTGGACATTTG | 26259 |
rs535507319 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910401 | CCAATCCCATCCAGG[C/T]TGCTACGAATGCCAT | 26259 |
rs535552084 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963583 | AACTCTAGCCTGGGC[A/G]ACAGAGTGAGACCCT | 26259 |
rs535563108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943685 | TCTGGTCTTTCCTGG[A/G]CACACACATAGCCCT | 26259 |
rs535569990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010631 | AGGTAATAGTTGGAT[A/G]TAGCTATGTCTCTGC | 26259 |
rs535586553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951655 | TTTCACATCATTGAT[G/T]GAGAGCAGAATCTCT | 26259 |
rs535627795 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939066 | CCGGTAACCCAAATC[A/G]GTGTTCTCTAAAGTG | 26259 |
rs535655795 | snp | G/T | 0.00318978 | 0.0398085 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911150 | AGAGGCGGGCTCGGC[G/T]GCCGGAGGTGGGCTC | 26259 |
rs535668958 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913079 | GTTGGCATAAGAATC[A/G]CTTGAGGCTTGGTTA | 26259 |
rs535732545 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015492 | TATTCTGTAGCTCTC[A/G]GGCTTCTCATCTGTG | 26259 |
rs535741063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116974270 | ACTCTGCACATGTGT[A/G]AGAGGAAATACCTGG | 26259 |
rs535771786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942183 | ACAGGCACACACCAT[C/T]ACATCTGGCTAATTT | 26259 |
rs535852422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947600 | CGAAAATTAGCCGGG[C/T]GTGGTGGCACACACC | 26259 |
rs535875273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958130 | AAGGTCCATTAAGAC[A/G]TTCATTATTTTTCAA | 26259 |
rs535887427 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946500 | GTATCTCTGGCCTCT[-/C]CCCATTAGACGCCAG | 26259 |
rs535897215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933402 | CTGGTTTTCTCATCC[A/G]AAGAGTTTATCAGAG | 26259 |
rs535897652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941207 | AGGATTGCCTGGGCC[C/G]CATTGGCCAGGGATG | 26259 |
rs535910391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954929 | ACTGTGCTGCACTCT[C/T]AGAGGTCACCCGTGA | 26259 |
rs535958483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940484 | ATAGTGTGGTGGAAG[A/G]ATGGTGGGCTTTTTT | 26259 |
rs536004600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982100 | TCCAAAAAATAAAAA[A/C]GGCAACAAAAGAGGA | 26259 |
rs536066805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116989224 | TTACTCCATAATGTG[A/C]CTTGGAGAGAGGATT | 26259 |
rs536076958 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032120 | TTGTGCATTTGTATG[A/G]TTATGGGAGGCAATT | 26259 |
rs536123085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023204 | GTCAGGGCACGGGAC[A/G]TGTTTCAGAGAATCC | 26259 |
rs536137894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970881 | AGTTCTTGCCTGGTA[C/T]CTTTGCCTACTCACC | 26259 |
rs536148392 | snp | C/G/T | 4.94664e-05 | 0.00497305 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028060 | GCGCCTATGAGTTTG[C/G/T]GGTGGACCAGCTGGC | 26259 |
rs536160169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022568 | GCTGAGGTGGGAGGA[A/T]CACCTGAGCCCAGGA | 26259 |
rs536176334 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933630 | TGTTAGAGCACATAT[A/G]TAAGAATAGAAAATA | 26259 |
rs536190826 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019267 | CTGGATGGACTTGTT[A/G]TGGATCTCAGAATTT | 26259 |
rs536210913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984352 | ACCACCCTGGAGAAA[A/G]GGTGTGTGGCCAGTG | 26259 |
rs536224606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955244 | GACCACTTAGCAAGG[A/G]TATGCAGCAGCGCAG | 26259 |
rs536237445 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024063 | AGTGTTGTGCATAGA[A/C]CAGCACCGTGGAGGG | 26259 |
rs536257100 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002397 | GAATTTGAGCATGGA[C/T]GGTGCCAGAAGCATG | 26259 |
rs536260147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000044 | TGGAGCGCAGTGGCG[C/T]GATCTCTGCTCACTG | 26259 |
rs536270919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991747 | AACTGGGATTTAGCT[A/G]TAGTCCATTATTGAT | 26259 |
rs536308908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926052 | GGAGGCCAGGCCAGC[C/T]GAGTAGGCAAAAGAC | 26259 |
rs536325279 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952353 | ACGACTGTATAATTC[A/G]TATGCCATAAAATTC | 26259 |
rs536332850 | snp | C/T | 1.74424e-05 | 0.00295312 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985199 | TGCATTGTTTCTTGC[C/T]GCATAGGGTTTCTTA | 26259 |
rs536352665 | snp | C/G | 1.64882e-05 | 0.00287121 | missense, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024301 | CGGATGAACCAGAAG[C/G]TGTGGGAGGTGTATT | 26259 |
rs536367930 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029244 | TAGAATCCCCCAACC[C/G]CAAGACACTGCACCC | 26259 |
rs536396246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992985 | TCTGCTTTTAGTTAT[C/G]TGAGAAATCTCCATA | 26259 |
rs536402858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986445 | CATCCTGGCTAACAC[A/G]GTGAAACCACGTCTC | 26259 |
rs536427721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018652 | CAGAAAAATGTTTTT[C/G]CTTTTTCCCAGGGGG | 26259 |
rs536448180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920294 | CTTACATGCGGTCTT[C/T]GTTGGAACGGTCTGC | 26259 |
rs536476805 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024403 | GCACCAGGCACGGTG[C/T]TAAATGCCCCCTACC | 26259 |
rs536507169 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013084 | CCCCGTCTCTACTAA[A/C]ATACAAAAATTAGCC | 26259 |
rs536519294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020267 | TAATTATCTTTCCTT[A/G]ATAGGTAATGTCTTT | 26259 |
rs536542633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979291 | GGCCTCCTTAGGGAG[G/T]TGGGAGGGGCCTGCT | 26259 |
rs536583154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920833 | TGCCTGCAGTGTTTG[A/G]GACCCTTAATGTGAA | 26259 |
rs536625918 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973151 | AAAATAGGAATATAT[A/G]AGTATATCATGATAA | 26259 |
rs536631210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939426 | TCTGCAGCGAGGAAT[G/T]CTGCTTCGTTTTGTT | 26259 |
rs536632575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928951 | GAGTAGCTGGGACTG[C/T]GGGCATGTGCTGCCA | 26259 |
rs536672527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980499 | TTCCTTACCATAGGG[C/T]ATAGAGAGGGAAAAG | 26259 |
rs536679658 | snp | C/G | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028099 | GCCCTCTCCCTGTCT[C/G]CCGTTCATCCTGTGA | 26259 |
rs536699337 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922494 | CATGTCCTCTTTGCC[C/G]TGGAGATGTACATTG | 26259 |
rs536717323 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022451 | CTTGGCCCAGGAGTT[C/T]GAGACCAGCCTGAGC | 26259 |
rs536743457 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021682 | TTTATATTTGACTCT[C/G]TGTTACTGAATTCTC | 26259 |
rs536774889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925636 | TCATAATTCTGAGAG[C/T]ACAGTGACTTTTTTT | 26259 |
rs536782780 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921362 | TTAAATGTTAAGAGA[C/T]GAATTGTTTTTTTGT | 26259 |
rs536841700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015373 | AGAGGCAGCAGTGGG[C/T]TTACTCCGTTCTGGC | 26259 |
rs536850228 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916865 | CACCTAGGCTGCTCT[A/G]CTTCTAGGGGTTGGC | 26259 |
rs536853416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926799 | TTTGCAGTTAAATAC[C/T]ACATTTCCTTTTTAT | 26259 |
rs536855120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923904 | TTTTTTATTAGAGAC[A/G]GGGTTTCACCATGTT | 26259 |
rs536880703 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000213 | TATCTCCTGACCTCA[C/T]GATCCGCCCACCTCG | 26259 |
rs536885472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116974138 | AGGCCCCAGTGAGGG[C/T]TCAGGGAAGCCAAGG | 26259 |
rs536922692 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909434 | GGAGTTCAAGACTAG[C/T]CTGGCCAACATGGTG | 26259 |
rs536928411 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997771 | AGGTATAGCGGCCCA[C/T]GCTGCTTCACAGGAT | 26259 |
rs536952751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962160 | CATTTGATTTTAGAC[A/G]TGTGGAGTCACAGTG | 26259 |
rs536958129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954137 | AAAAAAAAAAAAAGA[A/T]AAAGCAGTGGTAAAA | 26259 |
rs536988149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917472 | TTCCTCCCTGCCCCC[A/G]TTTCTTCTCCAACCT | 26259 |
rs536990421 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956500 | AGCCCCATTCATACA[C/T]CCTGGCGTCAGAGTG | 26259 |
rs537019860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964356 | AGTGGGGCTTATACA[A/G]ATTTCTGCAAGTGAT | 26259 |
rs537026241 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942541 | ACCATGTCCAGCTAG[-/T]TTTTTTATATTTTTA | 26259 |
rs537035119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936412 | CTTTCATGATAAAAC[A/G]CCCTTTGCCGATGTG | 26259 |
rs537045378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027094 | TGCATGTGGCTGATT[C/T]GTCTGCAGTAGGGTG | 26259 |
rs537077882 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031516 | GTCAGGAGCTCAAGA[C/T]CAGCCTGGCCAACAT | 26259 |
rs537081407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963477 | GACATGGTGGTGCAC[A/G]CCTATAATCCCAGCT | 26259 |
rs537095602 | in-del | -/G | 0.482757 | 0.0912364 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955036 | TTCCCCTCTTGAAAT[-/G]GGGGGGGGGGGGCCC | 26259 |
rs537115008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923584 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 26259 |
rs537180746 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007613 | CGGGATTTGTGCTGG[C/G]GTAGGTTTTTCCAGC | 26259 |
rs537211439 | in-del | -/GAG | 0.0517044 | 0.152246 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021583 | GAGAAAATTATTATA[-/GAG]GAGTATTTTGCCTCT | 26259 |
rs537215703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966919 | AGACGGGGTTTCACC[A/C]TGTTGGCCAGGCTAA | 26259 |
rs537241275 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924246 | ACTTTTTGGATGGCT[A/G]TGTGCTTCGCAGTAG | 26259 |
rs537255344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994481 | ACTCCTTCCCACTCC[C/T]TCCAACCTGCCACCC | 26259 |
rs537287804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949412 | CTCGAGTTCAGTGCC[G/T]TTGGGATATATGGTA | 26259 |
rs537318174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002958 | TGTGGATCTTACTTT[C/T]GTTGGGTCAGAATAG | 26259 |
rs537331698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995991 | CCTGAATTAAATTCT[C/G]CTCTCAGAGGTGGAG | 26259 |
rs537346416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958942 | GATTTGACACACAAA[C/T]GAAACCATTTGCTGT | 26259 |
rs537346538 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917041 | CAGTGGCCAGATGCA[A/G]TGGTGCTTTTGAAGT | 26259 |
rs537394901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995290 | TTTAATCTGACCTGC[C/G]TCTTCTCTTCTGTAA | 26259 |
rs537444274 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939651 | TGGTTTCTACAAAAA[A/C]GGCATATGTATGCCC | 26259 |
rs537446598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919343 | CAAGCAGACCTGAGT[G/T]CAGATTCTGGCTCTG | 26259 |
rs537451281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922328 | TGTGTGGGTCTACTC[C/T]ACTCAGCTTTTGCAG | 26259 |
rs537460180 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913431 | ACTGTTGACCAGAAG[C/G]CTTATAGATAAGTCA | 26259 |
rs537522708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008050 | ATGATGAATTTGCAG[A/T]GAGTCTTTTTGGAAA | 26259 |
rs537550508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953162 | CCACCTATATATGAT[A/G]TTATATGGGAAACTA | 26259 |
rs537619995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946939 | GAAAGGAGAGATACT[G/T]TTGAGATTTACAAGC | 26259 |
rs537661251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001926 | GAACCATATTCTGCT[C/G]ACTCCACAAAGTAGG | 26259 |
rs537677610 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019781 | CTTGTTTTTTAAACA[A/T]GGCAGCGTCCAGAAT | 26259 |
rs537690787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953837 | AAAAACAAAACCAGC[C/T]GGGCATGGTGGCTCA | 26259 |
rs537691759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957071 | ACCTTGTTATTAGCC[A/G]GGCACAGTGGCATGC | 26259 |
rs537697763 | in-del | -/T | 0.439918 | 0.162576 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976451 | GTTTCCAAAGGATCC[-/T]TTTTTTTTTTTTTTT | 26259 |
rs537726652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984475 | ACAGGTTTTAGAGCT[A/G]TGCAAAATAAAGCAC | 26259 |
rs537758714 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942864 | CTCACTGCAACCTCT[A/G]CCTCCCGGGTTCAAA | 26259 |
rs537763092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939469 | TCCTAAGCTCATTTG[A/G]GCGTGGAATCCTTTT | 26259 |
rs537916827 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912294 | CCTGGCTCAAGCCAT[A/C]CTCTTCCCTCAGCAT | 26259 |
rs537967444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937217 | CATGTGTGGGTATGG[G/T]GGAAGATCACTCATT | 26259 |
rs537969480 | snp | C/G | 0.00199481 | 0.0315187 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032763 | AGGGTTTCAGCTGAT[C/G]GGAGGGAAACTGAAT | 26259 |
rs537969826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011516 | CTCCTCAGTGTGTGT[A/G]TGGGGCACGCACTGG | 26259 |
rs537974469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117004646 | ACCTGAGGCAGACAC[A/G]TTTCTGGGTAAGCTC | 26259 |
rs537978133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116911282 | AGGACGTAGCGAGCC[C/G]CTCACGTTCTCCTCT | 26259 |
rs538009581 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012290 | TAAGCCAATGTTACA[-/T]TTTTTTTTAAAACGC | 26259 |
rs538071176 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032698 | GAGATACTCCAGGGA[C/T]GGCATCACCTTCTCC | 26259 |
rs538081569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946569 | ATGCCCCTAGACATT[G/T]CTGGATGTCCCCTGG | 26259 |
rs538148259 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967990 | TCAGGCTGGTCTCGA[A/C]CTCCTGACCTCAAGT | 26259 |
rs538155725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975721 | GCACTGGGAAGGCAC[A/G]ACACCTTCTGATTTT | 26259 |
rs538164691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023956 | ATGTGCTTTTAAACC[A/G]TTCAGATGAGACCGT | 26259 |
rs538178858 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926581 | CCTGACATTAAACCA[A/G]TGACTTTCCATTATT | 26259 |
rs538202415 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027968 | TGCACAGACAGAAGC[A/G]GCTGGGGTGAGGGCC | 26259 |
rs538207474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003891 | TGTGGTTTCATGCCA[A/G]TGTCTCTTTGTATGT | 26259 |
rs538207943 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029827 | ATGTTGGCCAGGCTG[G/T]TCTCAAACTTCTGAC | 26259 |
rs538240663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926155 | TGCCTCATCAGAATA[A/G]CATCAAGTCCAGACA | 26259 |
rs538252445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996947 | GTGTTGAGATGGAAA[C/T]GAGGTCATAACAAGA | 26259 |
rs538294383 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948174 | GGAAATGATTTGCTA[A/G]ACTAATTGTGGTGGC | 26259 |
rs538298241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934871 | ACCACCGCAGTCAAC[A/T]TGTAGAACATTCATC | 26259 |
rs538361399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934114 | GGCCTTTGAGATTTA[A/T]TTATCCCACAAACCA | 26259 |
rs538397313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975125 | AGTAGTTGAATTGCT[A/G]TATGGGAAAGGATGA | 26259 |
rs538428348 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951269 | TTAGCATGAGAGACT[C/T]CAGTCTTGCTTGTAT | 26259 |
rs538429387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023251 | TTGGGTCAGACGTGC[A/G]TTTTTAATCTTACAT | 26259 |
rs538439231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928203 | CTCCGGGGTAATAGA[A/G]ATTTACTCACAGAAT | 26259 |
rs538443441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026586 | AGCCCACACAGGCCT[C/T]GTCCCCTCCTGTGCA | 26259 |
rs538463157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982976 | CAAGTCATGACATAA[C/T]AAGTGGCTTTGGACC | 26259 |
rs538466180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027819 | GTCCTTGCCCTGTGA[C/T]ACTCACTGCGCCCAT | 26259 |
rs538481783 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028256 | GCACCTCTTCACAGG[C/T]GGTAAACATTTAGGG | 26259 |
rs538489224 | snp | A/C/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979965 | CCCAGGCCCTCTCCA[A/C/G]GTGGGCATGTTCATA | 26259 |
rs538496364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense, synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116918710 | CTCGAATCCATTGCC[C/T]ATTCCTGAAGATGAA | 26259 |
rs538523775 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914998 | GTTTAGAGACATTAT[C/T]GTCTTCATTTCTCCC | 26259 |
rs538546321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964430 | GTAAAAGGAAAAGCA[A/G]GGAGATCTTGCTACC | 26259 |
rs538563067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953157 | CCCTGCCACCTATAT[A/G]TGATGTTATATGGGA | 26259 |
rs538604519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949226 | ATCATGTAATACTTT[C/G]TTTTTGCTGAACGGA | 26259 |
rs538707378 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025442 | TTGTTCCCCACTTAC[A/C]GCAAATCAAGGTAAA | 26259 |
rs538713681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986494 | TTAGCCGGGCGTGGT[A/G]GTGGGCGCCTGTAGT | 26259 |
rs538722273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920950 | CCTGTCTTCTCTCCT[C/T]GCCATGTCCTAAAGC | 26259 |
rs538766147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018839 | GACCAAATTTGTGTT[G/T]GCCTTTGTCTCCTTA | 26259 |
rs538791510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980130 | CCTGGAATGGGGACA[C/G]CCACCTTTCTCCATG | 26259 |
rs538802315 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030078 | GAGTCCTCTCAGTTG[C/T]ACACGTGTACGTATC | 26259 |
rs538803079 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989369 | TGGCTGCTATAAGCA[A/G]TGCTACAATGCATAT | 26259 |
rs538838278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012917 | TTTAAGTAGTTTGCA[A/T]ACATGGGTGGAATTT | 26259 |
rs538851988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979358 | CAGGCTTTATGTCTC[C/T]TCGAAAGACTGGCCA | 26259 |
rs538889083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014390 | CAAGTTCTTTAAAGT[C/T]GTTGAGGGTTCCCAA | 26259 |
rs538913649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972414 | TATTTCATTCTGAAC[C/T]CTAGGGCTTGATCAA | 26259 |
rs538934252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020876 | CCAGCATTTTTAAGC[A/G]TTTTACAGTGGAACT | 26259 |
rs538947694 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990000 | TATTCCTCCCACCCA[C/T]AGTTGGATTCCAGCC | 26259 |
rs538949572 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013625 | TATATTAAAAAAAAA[A/T]TTTTCACATCTATGA | 26259 |
rs538974857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006617 | ACCAGCTGCCAGGAC[A/G]TGGCTAGAAGATGAT | 26259 |
rs539006862 | snp | A/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024651 | TTTTAGGATTTCTCC[A/T]TCTTAATAAACAGAA | 26259 |
rs539027338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926320 | GATAAGGAACATTTT[C/T]CTCTTGTTTCTTTAC | 26259 |
rs539029177 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933270 | TTACACAAAGTCAGC[A/T]TTAGATGATAAAATC | 26259 |
rs539058681 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982001 | AATCCAAAAGCAACC[G/T]CTAAAATAACAAAGA | 26259 |
rs539058950 | snp | A/G | 1.66632e-05 | 0.0028864 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024361 | GGAGTTCCTAGTAGG[A/G]ACAGGGAAGGCAGCA | 26259 |
rs539072069 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029121 | TGGATCCAGTAGATG[C/T]GTATGGAATTTCAAA | 26259 |
rs539093866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019541 | AAGAAGAAACAGTCT[C/G]TCCTCTGTGTCCTAA | 26259 |
rs539098377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021824 | AAGTAATGGTGGTGC[C/T]AGTGCCTCACTGTTT | 26259 |
rs539100799 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013903 | GGAAGTAATCACTTG[G/T]TTTTTTTTTTTGGTT | 26259 |
rs539112816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015955 | CCTTTTATGACTGGC[A/T]TATTCCACTTAGCAT | 26259 |
rs539145675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002173 | AGCAGTTGGCACTGC[C/G]TGCCCGGGAAGAGTC | 26259 |
rs539162059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926920 | ATCAGTGCTTGGACT[A/C]CCTTAAAAACATTGA | 26259 |
rs539238917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010512 | CAAGGCCCGGCCCCC[A/G]CTGCGCTGCTCACAC | 26259 |
rs539239035 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003101 | GTACTGAATAAAAGT[A/G]TACCTGGCACTTAGC | 26259 |
rs539259943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918508 | TCTTAATCCTGCTTT[C/T]CTTTTGTTGACTTTA | 26259 |
rs539274716 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951104 | CTTCTCTCTCTGCCT[C/G]TCTGTTCCCTCGGGG | 26259 |
rs539301176 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913698 | AGAGGCAGGCACATT[C/T]GATGCAACGTTTATG | 26259 |
rs539307787 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938703 | TTGAGATTTTCTAGT[C/T]TGTAATCATTGAGCA | 26259 |
rs539335014 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979375 | CGAAAGACTGGCCAT[C/T]GTTACTCATGTCATC | 26259 |
rs539342438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955309 | AGATAAGTGGACGTG[C/T]CTTCAACTGCGACTG | 26259 |
rs539371627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116974221 | GAACCCCAGGGATTG[G/T]CTGAGGATTCCCTCG | 26259 |
rs539392746 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910367 | CATTCCTGAGTTACT[A/T]CACTTAGAATAATAG | 26259 |
rs539414670 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014302 | TTTATATATAGTTTC[C/T]GTGTCTCTGCTGAGG | 26259 |
rs539417991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022481 | CAACACAGCAAAACC[A/G]TCTCTACTGAAAATA | 26259 |
rs539423637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957190 | CTTCTCTACCAAAAA[C/T]ACAAAAATTAGCCAG | 26259 |
rs539432803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923625 | GCCTGCCGGGTTCAC[A/G]CCATTCTCCTGGCTC | 26259 |
rs539432845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930199 | TACCCAGCAACCAGA[A/G]TTGCTGAATCATATG | 26259 |
rs539496120 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012042 | TACCACACCATTTTA[C/T]ATGTAAAGGGAGACT | 26259 |
rs539508336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967126 | TCTCGCATTTTACTC[A/G]TGGGGGGTCCTGCTC | 26259 |
rs539511252 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995459 | TTCTGAAATGGGCCG[A/T]GGAATCCATTATTCT | 26259 |
rs539537528 | snp | A/C | | | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977451 | ATGGTTATTCTTAAA[A/C]ATCTTTTATTGTGAA | 26259 |
rs539550223 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991558 | CAGCCTGGTGGCAGC[A/G]TGTGTCCCAGCACGT | 26259 |
rs539575168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002001 | AGAGAGAGATTGGCC[A/G]GTTTGGATGGTTTTT | 26259 |
rs539597016 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962447 | GAGGCCACCTAAACC[A/G]TCTTTCCTCTCCACC | 26259 |
rs539607826 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980614 | CCTTTCAAATGAATT[-/TA]TATCAGATTTAAAAA | 26259 |
rs539688584 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936812 | AAGAGGAGGAGAGGA[A/C]TCAGGATGTGATAAG | 26259 |
rs539692807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942923 | GCTGGGACTACAGGT[A/G]CGTGCCACCATGCCT | 26259 |
rs539693255 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993556 | GAGAAATATCTGTTC[A/C]TGTCATTTGCCCACT | 26259 |
rs539696806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937093 | ATTGTGGATGGGCTG[A/G]ATGTGGGGACAGAAG | 26259 |
rs539721137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116989053 | CATTTTCTTTCTCCT[C/T]CCTTCCCCCAACTTC | 26259 |
rs539733099 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936251 | AAGGACTTGAGGCAG[A/G]CACAGCTGAAGCTCA | 26259 |
rs539755988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952412 | TTTTTCTTAGTAGAT[A/T]TACAAGGTTGTGCAA | 26259 |
rs539813656 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982399 | GATACCGAGGGACTT[C/T]GCCTGTGATAAAGAA | 26259 |
rs539824964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915945 | TGTGAGCCTGCATGC[C/T]TGGCCTCACCTGACT | 26259 |
rs539874525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945789 | TGCCAGCCACTTCCT[C/T]TCGGATTGTTAGGGT | 26259 |
rs539876312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953268 | ACTTTAGAGATGATG[C/G]GTTCCAAGACCCTCA | 26259 |
rs539881626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008025 | CTGGACTACTAACTT[A/G]GATGTCTTTATGATG | 26259 |
rs539909149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002456 | TGCAGGGAACGTTGA[A/G]GGGGTCAGGGATCCA | 26259 |
rs539937878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956206 | GCCTTTTTAGCATAC[C/T]GTTCCTGCCTTTGCT | 26259 |
rs539959689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939108 | GCACTGGGCTTTTGA[A/G]ATACTCGTTGCAAAA | 26259 |
rs539965268 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020410 | GTCTTTCATCAGTTC[A/G]GGAAACATCAGCTGT | 26259 |
rs539969320 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009021 | GCAGTGAGCCAAGAT[A/C/T]GCGGCCACTGCACTC | 26259 |
rs539999602 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031589 | CCTGGTGGCGTGTGC[C/T]TGTAATCACAACTAC | 26259 |
rs540001089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943459 | TGCACCTCCTGAAGT[C/T]TCTGCTTGGCTAGCT | 26259 |
rs540029840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996106 | AGGGCTCTTAGCATC[A/G]TTCTATGTATTTGGA | 26259 |
rs540034736 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956469 | GGCCTGATTCAAATA[C/T]GTTTTTATTTTTCTG | 26259 |
rs540043054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976189 | TTAATGCCATTTAAA[A/T]ACAATGTTACATGAT | 26259 |
rs540092304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929434 | GAGACACGATTTTGT[C/T]ATGTTGGCCAGGCTG | 26259 |
rs540115422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011838 | GTGGAGAAGAAACCT[C/T]TGTTTTCTGCATAAT | 26259 |
rs540160580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027107 | TTCGTCTGCAGTAGG[A/G]TGTGCCCTTTATGTC | 26259 |
rs540177935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116976844 | CAAAAAAAATTTATC[A/G]GTTTCATATATAAAA | 26259 |
rs540289789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924906 | AAACCTTGAATTTAC[C/T]CTGGTTTGTCTGGTG | 26259 |
rs540305607 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022548 | TAGTCCCAGCTATTC[-/G]GGACGCTGAGGTGGG | 26259 |
rs540403563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932812 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC | 26259 |
rs540410245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925678 | TGGCTGTGTAATGTC[A/G]TTTACAAAATTACAA | 26259 |
rs540418572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024399 | GCCTGCACCAGGCAC[A/G]GTGCTAAATGCCCCC | 26259 |
rs540425820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984582 | TTCCAAAATGCTTTG[A/C]AACTGTTTAAGCACT | 26259 |
rs540430910 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960207 | CATTTAGGGTTTGGT[A/C]CAGGTCCCTCTGCCC | 26259 |
rs540459883 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028573 | TACCTCTTTTCCTCC[A/G]AGGGCCTTTGGATGT | 26259 |
rs540488064 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968062 | GCTTGAGCCACCGCG[A/C]CTGGCTTGTCATTTA | 26259 |
rs540490977 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920426 | AAGGCAGAAAAAAGC[C/G]TGTGCCCTTGTGTAA | 26259 |
rs540554024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919850 | TGGCCAATATTTATC[A/G]CTCACCATGTCAATA | 26259 |
rs540563430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968928 | CTTGGATTAGCATGC[A/G]GTATGGTTCCAAGTA | 26259 |
rs540604449 | snp | G/T | 0.0178098 | 0.0926698 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029478 | GGCTGGGAGGGGCTG[G/T]GAGGGGCTGGCACCT | 26259 |
rs540611091 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116949872 | TTCTGTTCCCAAGGA[C/G]GTGAGAGCGCGCAGC | 26259 |
rs540611411 | snp | C/G | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022958 | CAGCAGACACACCAG[C/G]TCCCACTTAAGCCAT | 26259 |
rs540635344 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982367 | TGGATTTCAAAGCAA[A/C]GACTATAGTAACCAG | 26259 |
rs540653852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025601 | GTGTTGGCAAACACT[A/G]TGGCCGGCACATTTT | 26259 |
rs540678913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918000 | CCACCTCAAAAAAAA[A/C]AAAACAAAAAAAAAA | 26259 |
rs540727501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007189 | TAGATTTCAGATACA[G/T]CAGAATCATTGACAA | 26259 |
rs540730177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020409 | TGTCTTTCATCAGTT[C/T]GGGAAACATCAGCTG | 26259 |
rs540745102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015746 | CAATTCAGTGTTTTA[A/C]GTAGGTCCACAAGGT | 26259 |
rs540746914 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925412 | GGCAAGGACCATTGA[G/T]AGAATATGTTGCCAG | 26259 |
rs540750573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921899 | CAGTGGTGTGATCAT[A/G]GCTCTGTAGCCTTGA | 26259 |
rs540764050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963711 | TCAGTGAATCTCAGA[G/T]GTTATCTCATCAACT | 26259 |
rs540790705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013323 | GGAAACTGAGTTAAT[A/G]TTAGAGTATGCTTTT | 26259 |
rs540828806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010833 | ATGTTCAGCAAAATA[C/G]GGTTTCCTGCCAAAC | 26259 |
rs540892656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998111 | GGTGTGAGCCACCGC[A/G]CCTGGCCCCCAAGAA | 26259 |
rs540902105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004799 | CTCTCCTGTTTCCCC[A/G]GCTCTCCAGGCTCCT | 26259 |
rs540924460 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029111 | GCTAACAAGCTGGAT[C/G]CAGTAGATGCGTATG | 26259 |
rs540938151 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922565 | TTTGGCTCTTAGTAA[C/T]TATCTGTTCTTCTAT | 26259 |
rs540963249 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004117 | CTGTCTGTTGCATTC[C/T]GCCCAATTCCTCAAC | 26259 |
rs540968091 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017015 | TTCTGGCACTACCAC[A/G]CTGTACAGCTTTTTG | 26259 |
rs540985740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971121 | GTGGCTCAGGCTTGT[A/G]ATGCCAGTGCTGTGG | 26259 |
rs541006491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936828 | TCAGGATGTGATAAG[C/T]GTTTAATCCATTAAA | 26259 |
rs541062569 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912615 | ACAGGCGCCCACCAC[A/C]ACGCCCGGCTAATTT | 26259 |
rs541067553 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935317 | GTGATTTTATGTCCA[C/T]GTAGGAGAAACTAAA | 26259 |
rs541076300 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941539 | GGCCAAAACTTTAAT[-/A]GTGTCGTCAGTGTTA | 26259 |
rs541084019 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116916543 | TGTAAGGTCTTTAGA[-/T]TTTTTTTTTTAATTG | 26259 |
rs541086943 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961865 | TGTTTTGAAGGGCTT[A/G]GCTTGTGGGGGGAGG | 26259 |
rs541101735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000150 | CCACGCCTGCCTTTT[C/G]TATTTTTAGTAGAGA | 26259 |
rs541145363 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116914251 | GCACTCCAGCCTGGG[C/T]GACACAGCAAGACCC | 26259 |
rs541165189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999719 | AGACTGTGGGGAGTC[A/G]GGCCCCATCTTAGCT | 26259 |
rs541236176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940621 | CAGGAGTTTTAAGCT[A/G]ATTAGCAATCTTTTC | 26259 |
rs541252434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964507 | GTGAGAATGTGAAGC[A/G]TGTTCACAGCCTTCT | 26259 |
rs541307797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994907 | AAGGGACATGTGCCT[A/C]CATGATTTTGATAGA | 26259 |
rs541341664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025204 | TGTGAAGAGACATTC[A/G]GCCAGACACGTGGCT | 26259 |
rs541413266 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012303 | CATTTTTTTTTAAAA[C/T]GCTCTGTCTCTGTGG | 26259 |
rs541456768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010109 | GAATTCGCTGGATTT[C/T]CTTCTCTCTTCCTTT | 26259 |
rs541491211 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992172 | CTTATCTGTCTAATC[-/T]TTTTTTTTAAAAAAG | 26259 |
rs541526511 | in-del | -/A | 0.172997 | 0.237846 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910079 | CTCTTTCAGATTTTT[-/A]AAAAAAAAATTTTTA | 26259 |
rs541534575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947299 | GCAGGCTGAACCAAA[C/G]ATGAGGGAGACTTCT | 26259 |
rs541547606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913150 | TCACCAGGGAAGGGG[C/T]CCTGAAATCTGATGA | 26259 |
rs541556456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996429 | AGAAATGCAGTGCGC[A/G]TAGATTGTGGCCACA | 26259 |
rs541565078 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952005 | ACAAATAATTTCTAG[G/T]TAACTTTTCCTGACA | 26259 |
rs541595492 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909635 | CTCCGTCTCAAAAAC[A/C]AAACAAACCAAACAA | 26259 |
rs541613955 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032930 | ATGGCAGACACTGGC[C/T]GCCGCAAACCCACTT | 26259 |
rs541640625 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962941 | GAAGGGTGAGCTGAC[C/T]GCTGCTTGGAGAGCC | 26259 |
rs541640995 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913921 | GAATCACCACATTAG[A/G]TACTACTAGGTTCTC | 26259 |
rs541676441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947724 | AGCCTGGGCGACAGA[A/G]CGAGACTGTCTCAAA | 26259 |
rs541728889 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029962 | AACTCTTGATAAAAC[A/G]TAAAGGTACAGTGGT | 26259 |
rs541729637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977731 | TTCACGTTACCTGCC[C/T]TCTGGAACTTTCCCT | 26259 |
rs541740319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983124 | AGAAGCTCTATGCAA[A/G]TGGGAGTTTTTTTTC | 26259 |
rs541775134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027888 | ACTGTGAGTATCTGA[C/T]GCTGTGTGCCCAGAG | 26259 |
rs541777843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951434 | CACCAGGCTTTCTAC[A/G]GTTATGTATCTCCAA | 26259 |
rs541793623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942987 | TTTCATCGTGTTAAC[C/T]AGGATGGTCTGAATC | 26259 |
rs541815473 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960683 | GAGGTACCCCTCAAG[C/T]CAGTCAGGTTGTTAC | 26259 |
rs541830072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935359 | TATAGCTAAAGATCT[A/G]TAATCTTAATGAAGT | 26259 |
rs541854999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942333 | TCTTTTTTTTCCCCC[A/G]TAGAGTAGATAATCT | 26259 |
rs541864949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987114 | CAGTGGCAGTGTTCC[C/T]AGGTCTGCGATATTA | 26259 |
rs541899645 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030668 | GTAAAAATGTCCCAA[A/G]TGTAGCCCCTCCCAC | 26259 |
rs541917607 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964333 | AGTGTGTGCGTTTGT[A/G]GGTAAATAGTGGGGC | 26259 |
rs541949973 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944241 | TAATTTCCAGACTCC[A/G]AAAAAGTTGATCGAT | 26259 |
rs541965900 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027608 | TATGGGCTATACCCT[A/C]AGGCAGGGCCCTGCC | 26259 |
rs542019230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989684 | TACCAGTGGGACCAA[A/G]GGGGAGAGAGAGAAA | 26259 |
rs542023844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937423 | AGGCCGTGGACATGA[A/G]CAGGGCCAGGCAGAG | 26259 |
rs542039358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972837 | ATGTTTATGTGTGTC[A/C]TGGCTTTGTTTGCTG | 26259 |
rs542040485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014651 | GCAAGTTCTGTTTAC[C/G]CTTTGTGGGTGGTGA | 26259 |
rs542053716 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032430 | ACAGACAGTGGCCCC[A/G]GCCGGGAATCAATTT | 26259 |
rs542059878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924306 | TTATTTATTTTTAAT[A/G]GACACATTATAATTG | 26259 |
rs542077332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981199 | GTAGCCATGATATAA[C/G]TGTAGTAACTGATAA | 26259 |
rs542091361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936642 | CTTTCTGAAGCCTCC[A/G]GAAGGAATGCAGCCC | 26259 |
rs542123179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930824 | TTTTTATTTTTTTTA[C/T]TGAGACAGAGCCTCA | 26259 |
rs542130216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116974756 | CTCCAAAAAAAGAAT[A/G]TATTGTGTACCCTGG | 26259 |
rs542151673 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014636 | GGTTAGGTTCAGACG[G/T]CAAGTTCTGTTTACC | 26259 |
rs542155950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982413 | TTGCCTGTGATAAAG[A/C]ATCAACTCATCAAGA | 26259 |
rs542195834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939644 | AATGTTATGGTTTCT[A/G]CAAAAAAGGCATATG | 26259 |
rs542217144 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028645 | TCCCTGTATTTACTT[C/G]GGGTGCTCTTCTGTG | 26259 |
rs542257009 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939183 | CAGGTTGAACTTCCC[A/G]AATCCAAAAATCCCA | 26259 |
rs542304864 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921024 | CAGCCCATTTTGCTT[C/T]ACACCACCCTCCTTC | 26259 |
rs542331542 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964204 | ATCAATTAGTCTTCA[A/G]GGACTTTAATCAGTC | 26259 |
rs542345627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116976964 | TGAGTCTCCGTCTCT[A/T]TTGGGCTCTTGTGAT | 26259 |
rs542353578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987644 | TGACACAAATGTTAA[A/C]ATTTTTTTTGCGAAT | 26259 |
rs542375107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961900 | AATGGAAGAAGCTCC[A/G]AATCAGGGAGCCTGT | 26259 |
rs542376513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024429 | CTACCCCCCGGCTTC[A/G]CCAGGTGAATCCTTA | 26259 |
rs542407043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984630 | AGGAAATTTCACATC[C/T]AACTTCATGTGATGG | 26259 |
rs542427820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923329 | AATACAGGACGAAAG[C/T]CCCCAATAGTGGTAG | 26259 |
rs542436532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969741 | GAATCGTATCCAGAG[G/T]GGGAGATGGAACCTG | 26259 |
rs542457570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929101 | ATGAGCCACCGCGCC[C/T]GGCCCCATTGATGGT | 26259 |
rs542467933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009491 | TCAGAACTTGGTGTG[A/T]TTGTGTGTGTGTTAA | 26259 |
rs542472714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021240 | CTTAAACATCTTACA[C/T]ATGTTTAAAAGCCAT | 26259 |
rs542473019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027155 | TGGGGGCAGATGCCA[G/T]CATGCGTACGGGGCA | 26259 |
rs542501501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917110 | CCAGAGTCAGTGTGG[A/G]TTTACCCAAGTGCTT | 26259 |
rs542510361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962513 | CTGAAAACAGTGTGC[A/G]GACTGCTGGTGTGGT | 26259 |
rs542513093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006371 | ATCCATTTCTTACTG[C/G]GTGAAGGAAGAAGTT | 26259 |
rs542564478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923683 | CGCCTGCCACCACAC[C/G]CGGCTAATTTTTTGT | 26259 |
rs542564516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116916483 | GGGTAATAACCACTG[C/T]CCCCATTAGCTGGTT | 26259 |
rs542640808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925149 | TAGGTGGTTTAGTGG[A/G]TTTTCCTTTCAGAGA | 26259 |
rs542643472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023460 | GTTTGTAGTGGATAC[A/G]AGATTTCTGTCCCAT | 26259 |
rs542702089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931311 | ATTTTGAAATGAGGT[A/G]TTGTGATGCCTCCAG | 26259 |
rs542713915 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011273 | TGCTCGGAGGCGGGT[A/G]TCAGATCGTGAGGCG | 26259 |
rs542717422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017148 | TGTAGGAAATACTCA[C/T]GACTTAGTTAATAAC | 26259 |
rs542735845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116918860 | GGTGTGTGACGCAGC[A/G]CTAACTGAGAATACA | 26259 |
rs542744139 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936234 | GTGGAATAGCAAGGA[C/T]GAAGGACTTGAGGCA | 26259 |
rs542787254 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011947 | GAATCATAATGAAGC[A/G]ATGTGTAGGCATTGT | 26259 |
rs542811397 | in-del | -/TTTTTTT | 0.479502 | 0.0991411 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915641 | CACTCACCTGACTAC[-/TTTTTTT]TTTTTTTTTTTTTTT | 26259 |
rs542820283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953343 | TGAGTGGAGCCGCTC[C/T]GCTGTGTTTCTGCAG | 26259 |
rs542831253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920601 | GGTCTTTCTGGGAAG[A/G]TCACATTTCATGGAG | 26259 |
rs542840282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025093 | CACCTGCCACCACCT[C/T]TACCTGGCCCTGCAG | 26259 |
rs542847065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004900 | CTTCATCTGGGTTTC[A/G]TGCTGTCTCCATTTT | 26259 |
rs542876071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018290 | GCTTTCAGACCAATT[A/C]TTTTTCCTTTCAATG | 26259 |
rs542994984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014089 | TTGTGAAATTTTCCA[A/G]CAGGCCACCAAAGCT | 26259 |
rs543017848 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928825 | GTCAACTTTCTTTTT[A/T]TTTGAGATGGAGTTT | 26259 |
rs543035159 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917034 | CGAGCCCCAGTGGCC[A/G]GATGCAATGGTGCTT | 26259 |
rs543064223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975298 | ATAAACAACAGAAGT[A/T]TATTTCTGACATTTC | 26259 |
rs543100337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939419 | CGCAAGTTCTGCAGC[A/G]AGGAATTCTGCTTCG | 26259 |
rs543126755 | snp | C/G | 0 | 0 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010890 | GGTGGTGTCCCTCTG[C/G]TGATGGAAGGAAAGA | 26259 |
rs543180346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923229 | AGGAGGTGCTTGAGC[C/T]CTAACCCTGGAAATT | 26259 |
rs543235635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952862 | CCTGCTTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 26259 |
rs543301058 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031335 | CAGGATCCAGGAGAC[C/T]CGCAACATGGTACAG | 26259 |
rs543314171 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918015 | AAAAACAAAAAAAAA[A/G]CAACGCAGGACTCCT | 26259 |
rs543364499 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015081 | CCTATTCTTTGAGGA[C/T]GGCAGGGGCCCCCTT | 26259 |
rs543394229 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922581 | TATCTGTTCTTCTAT[A/T]AAACAAGAGAAGACA | 26259 |
rs543443954 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000271 | GTGAGCCACCGCACC[C/G]AGCCTGCATCTCATA | 26259 |
rs543480075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955126 | TGAGCCAAGTGTGTA[A/G]GAAAGGAAAACTCCC | 26259 |
rs543532229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956653 | TATCATTGTTTTACA[A/G]TTAAGAAGTATTGGA | 26259 |
rs543541650 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017651 | ATTTCTTTAAAAAAA[C/T]ACTATTTTTAAAATT | 26259 |
rs543541748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965567 | CCACAAGCTTCATGT[C/T]CCCACTTGCCCAAAA | 26259 |
rs543573301 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998242 | GAAACCCTTCAAGAT[A/G]CGAAGCCTTATTGGA | 26259 |
rs543583163 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965072 | CACCCATTAAAACTG[G/T]TGTTTAATTCCTACT | 26259 |
rs543594105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002228 | AGGTGCATTGGCACG[C/T]GGTGGTGGGGAGCGC | 26259 |
rs543610345 | in-del | -/CTTCAGTTTTTT | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916584 | TTTTTATGTGGACTC[-/CTTCAGTTTTTT]CTGCATGAGAAAACC | 26259 |
rs543610840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025655 | CCTGGCCCGCCCCCT[C/T]GCTGTGGCTGTGCCT | 26259 |
rs543619399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986042 | ATGATTTGGTGTTAA[A/G]AAGGAAGTGCTCAAA | 26259 |
rs543635978 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994788 | TTGCTGGCTCCCTAC[A/G]GATGGATGCTAGATT | 26259 |
rs543658587 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116916115 | CTGTTGATGGGAATT[C/G]TTGCTAGTTTGTTGA | 26259 |
rs543670016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957341 | ACAGCGAGACTGTCT[A/C]AAAAAAAATTTTTTT | 26259 |
rs543702986 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030034 | TACCACATGGGAACC[A/G]TTTGTCCACACTCAT | 26259 |
rs543704129 | in-del | -/GTC | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001751 | TTCAGCTCCCAGTCA[-/GTC]GTCATACATTTGCAC | 26259 |
rs543705891 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987658 | AAATTTTTTTTGCGA[A/T]TTTGGAGCTGAATGT | 26259 |
rs543727165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019919 | TTTAAACAGGAAGTA[C/T]GCACATTCAAAATGG | 26259 |
rs543732347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000584 | CCCAGAGCAGCGGAG[A/G]CTGCTAGTCCTGGGA | 26259 |
rs543764887 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942303 | TAGGATTACAGACTC[-/T]TTTTTTTCCTTTATT | 26259 |
rs543766269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955690 | AAAGAGTAGAAGAAA[A/G]GGGCATATGGAAACA | 26259 |
rs543769024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995727 | TGACATACAGGACCT[C/G]ACAGGTAGTCACTGC | 26259 |
rs543794441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006759 | TTCTGCATGTCACCC[A/C]GCGTCCCTGCACGTT | 26259 |
rs543816184 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004980 | ACTGTTTGATGATAG[A/G]CTGAGTCTTATCCAG | 26259 |
rs543825382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952611 | CAACTCATCGTGTGG[C/T]CTTGCTGTTTCACTG | 26259 |
rs543830354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960048 | GTAACTGTCATAGTG[A/G]CATCTTAATTGGTTG | 26259 |
rs543837407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914157 | GCACCCCTTTAGTTC[A/T]AGCTACTTGGGAGGC | 26259 |
rs543882918 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027192 | CCTGTTTACAAAGTC[A/G]TGCCCAAAGCGTGGC | 26259 |
rs543902157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948377 | GTAGGACAGCTCCAC[A/G]TGGATGTGTCTAGTT | 26259 |
rs543928965 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000834 | TAAGAGAATATTATA[A/C]ATATTAGCTGTTATT | 26259 |
rs543934620 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940797 | GCAGAAAACCAGTGT[C/T]TGATAAGATCCTTCT | 26259 |
rs543974361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945756 | TTATTCTGCAGGAGA[A/G]GAAGGGTGAGATTGG | 26259 |
rs543988009 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000449 | AGGGGTTCTCACATG[C/G]CAGCATGCATCAGAA | 26259 |
rs544005748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998027 | TCACTACATGTTGGC[A/C]AGGCTGGTCTTGAAC | 26259 |
rs544045750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928489 | TTGGTTAAATCGAGC[C/T]TGTTATTAGGTTGGT | 26259 |
rs544072775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941404 | CACGTGATCTAACTT[C/T]GGATGCTGTGAATTC | 26259 |
rs544078724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979518 | CCCTTCTCCTTTATT[A/G]GGCCAGTGGTCCTCA | 26259 |
rs544104816 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937510 | GGACCATGGGATAAA[C/T]GTTTTCCAGGAGGAG | 26259 |
rs544132272 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979979 | AGGTGGGCATGTTCA[C/T]AGTATTTGAGTTAGT | 26259 |
rs544145583 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935085 | GTAATTTTAGGAATT[G/T]AGCTGCATAAGTAAT | 26259 |
rs544185954 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927256 | ATGACAGCCTTATCT[C/G]TCAAATAAAGCCCGT | 26259 |
rs544189318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997388 | AGTTCCTTTCAGCTA[C/T]AGTCAAGATAGCAGT | 26259 |
rs544200755 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032523 | TGTGAAATGGTGCAT[A/G]AGGGCATTTTCTGGG | 26259 |
rs544222012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952153 | AGTTAAGATACAGTC[A/T]TATGCTGCATAACAG | 26259 |
rs544237486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936177 | AGCTTTGAGCAAAGA[C/T]CTGAAGGAGGGGTGA | 26259 |
rs544247735 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031728 | CAAAAAAAGAAATGG[C/T]AACTTTAAGCAAAAT | 26259 |
rs544249619 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930596 | TCTCTTTTATAGGTT[G/T]TCTCTGTATTCTGTT | 26259 |
rs544262620 | in-del | -/C | 0.0134861 | 0.0810011 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017879 | CGCCCTGAGTTGTGA[-/C]CCCCCCAATTACAGA | 26259 |
rs544283370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980777 | GGGTCTTAAAATAGT[A/G]TGACAGCATGACCAA | 26259 |
rs544309225 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032966 | ACAGTTGCTGAGAAA[C/T]GGCTTCCCCTGGTGA | 26259 |
rs544356136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023586 | ATTTCAATAAGTGAC[C/T]GCCCAGGGTACACAC | 26259 |
rs544396348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939048 | CATATCTTAACTGAT[G/T]GACCGGTAACCCAAA | 26259 |
rs544399920 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027571 | TAGAACCCCACCCCC[A/C]CCGCCGTGACACATT | 26259 |
rs544400328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931436 | TGTCTTTGGAATTTT[A/T]ATAGAGATTGCATTT | 26259 |
rs544491884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959219 | CCAGTTGCAATTTAG[G/T]GGTCGAATTGATGGG | 26259 |
rs544511298 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925240 | ACAGGCTGCCTTAGT[G/T]GGGTGGGAGGGGATG | 26259 |
rs544527353 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923709 | TTTGTATTTTTAATT[A/G]ATTAATTAATTTATT | 26259 |
rs544535791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975399 | AGTGCCTTCTCTCAC[A/G]TGGTGGAAAGGGCAA | 26259 |
rs544536142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932059 | TCATGAAAGGATCTT[C/G]AATTTTGTCAGATGC | 26259 |
rs544556064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027177 | TACGGGGCATGCAGA[A/C]CTGTTTACAAAGTCA | 26259 |
rs544582005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933626 | CAGTTGTTAGAGCAC[A/G]TATATAAGAATAGAA | 26259 |
rs544589617 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116974421 | GGAATCTTCAGAAGG[G/T]TACCATGTTTTAGTA | 26259 |
rs544639590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025163 | GAAAGGCAGCCGGCC[C/T]TCTCGCTTGCTGCCC | 26259 |
rs544644913 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002333 | GGGCTTGTCACTCCA[A/G]TTAAAACTTAAACAT | 26259 |
rs544650969 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116972192 | TTCTATTTTATTACA[G/T]TTGAGTTACAAACTG | 26259 |
rs544651357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932972 | TTTTTTGATGCGGAG[C/T]GTGTGTCTTTAGGAA | 26259 |
rs544659386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927592 | TAGTTGAGAGTAGTG[A/G]TGGTTGTCCTGGGAA | 26259 |
rs544692204 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002637 | TATGACTTATCTCTG[G/T]CAAGGACTTACAAAA | 26259 |
rs544702489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027106 | ATTCGTCTGCAGTAG[A/G]GTGTGCCCTTTATGT | 26259 |
rs544709545 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947502 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCTGAGG | 26259 |
rs544753802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970430 | CATGCTCCATTGTCC[G/T]GGACTGTGGCTGCCC | 26259 |
rs544799795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019213 | CATTTGTAGCAACGG[A/C]CCTATTATGTATCAT | 26259 |
rs544807895 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007675 | GGTCATGGGTTGAGA[C/G/T]TCACCCAACTAGGGC | 26259 |
rs544818856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962565 | GCAGAAGGACAGAGA[C/T]TGGCAAGAAGGAAAT | 26259 |
rs544822088 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026689 | AACATCGCTCGTGCT[A/G]CAGAAACAATGGTCA | 26259 |
rs544841221 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004812 | CCAGCTCTCCAGGCT[C/T]CTGACACTGGAGGGA | 26259 |
rs544885181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010911 | GAAGGAAAGAGAGAC[C/T]TCATGTGAACAGATT | 26259 |
rs544885201 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909917 | AGTCAAGGTGGGGGG[A/G]AAAGTTCCCTGCTGA | 26259 |
rs544900341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955786 | GTTAAGTGTTGCAAT[C/T]AGATGACATCATGAG | 26259 |
rs544927657 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939969 | CCAGACATGCCAAAA[A/G]TAAAACCATGGTGTT | 26259 |
rs545027939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940567 | GACCAAATTGGGGTT[A/G]CTGTTGCGAGGAAGA | 26259 |
rs545065397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912569 | GGTTCACGCCATTCT[C/G]CTGCCTCAGCCTCCC | 26259 |
rs545065709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919748 | GACTTTATAAAGGCT[C/G]TATGATTGTTAGAAC | 26259 |
rs545172850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921113 | TCTTCTACCTTCTTT[C/G]CTTGCCAGAGTCCCC | 26259 |
rs545174115 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971781 | ACTGTGCTGTGGGAT[A/C]TCGGTACCAGAATTT | 26259 |
rs545182583 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957193 | CTCTACCAAAAATAC[-/A]AAAATTAGCCAGGCA | 26259 |
rs545261447 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012594 | AAGTCTTACATTTTT[C/T]CCCCGGAGGTTTAAT | 26259 |
rs545277591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007660 | GAGAATGAGTCAAGT[A/G]GTCATGGGTTGAGAC | 26259 |
rs545289075 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981904 | CAGGCATGAGCCACC[A/G]CACCCAGCCTAAAGT | 26259 |
rs545317574 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943735 | CAGACTCCCAGGAAT[A/G]TATTGGAGCCTTTCA | 26259 |
rs545335385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007090 | GAATATACAGAGGGC[C/T]ACCACTTCCTTTATA | 26259 |
rs545349058 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968839 | AAAAATGTGTACCTG[C/G]TACTTGTAGTTCTTT | 26259 |
rs545382724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961076 | ATCTCGGCTCACTGC[A/G]ACCTCCACCTCCCAG | 26259 |
rs545383079 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018076 | AGCGTGCCTCCCTCT[C/T]GGTTCCAGCACGTTT | 26259 |
rs545387636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939813 | CTCTGCTCTGGGACT[A/G]CTCAGGTTGTGGCCT | 26259 |
rs545394291 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000432 | CAGTATAGGTAGAGC[A/G]CAGGGGTTCTCACAT | 26259 |
rs545435255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966486 | TGTGTCTCCAGGGCC[A/G]TGCTGCGGTGGTCGT | 26259 |
rs545454036 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021907 | TCCATGGACGTGACT[A/G]CCTGGTTTTTCGTTG | 26259 |
rs545457671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015029 | TCCTTGGGGCACAGC[C/T]ACAAGAAAGAGAAAA | 26259 |
rs545507018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009296 | TACTCGGGAGGCTGA[A/G]TGGGAGAATTGGCTG | 26259 |
rs545513809 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920402 | GGCACTGAGAATATA[C/G]CATTGAACAAGGCAG | 26259 |
rs545519304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953395 | GGTGAGGCTGCCGTT[C/T]CCAGCCCTCATTTGC | 26259 |
rs545529321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002292 | CTCAGCAACACCGTC[C/T]CATCCCTGAAATATC | 26259 |
rs545577336 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969063 | TCTGTTTCTGAACTT[C/T]GTGCTCTGTTTCAGT | 26259 |
rs545610412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917002 | GCATTCTCAGAGTTA[C/G]AAGAGCAGCAAGAGG | 26259 |
rs545651077 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993142 | GACGTCTTGCTCTGT[C/T]GCCCAGGCTGGATTG | 26259 |
rs545685118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984862 | GGGTATGGTGGCACA[C/T]GCCTGTAGTCCTGTC | 26259 |
rs545685469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947674 | AACCCTGGAGGTGGA[A/G]GTTGCAGTGAGCCAA | 26259 |
rs545705098 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032399 | CTCTCCGACCGGGAG[G/T]ACGTCTAGACGGTGC | 26259 |
rs545707156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027229 | ACCTGAGCTTCGGGA[A/C]CTGAGGTGAGACACT | 26259 |
rs545714232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000074 | GCAAGCTCCGCCTCC[C/T]GGGTTCTCGCCATTC | 26259 |
rs545742081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992245 | AGGAAGGGATCAGAC[A/G]GTCTGGGCCCTGAAA | 26259 |
rs545747270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989583 | AATTCTTTGAGTGAT[A/G]ACTAAATTTTATCAC | 26259 |
rs545779431 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116916452 | CATTGGGAAATACAT[G/T]CCATGGCTGGGGTCA | 26259 |
rs545791160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987854 | CCCTCCTTGAAGGCA[A/G]CCATTGTTAGAAGAT | 26259 |
rs545800002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965639 | CATGGCACCACTGCA[A/G]ATCTTCAGAGTCAGT | 26259 |
rs545806624 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997170 | CTCCACAGAGCCCTA[C/G]AGTTTCTCAAGACAG | 26259 |
rs545828037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948680 | ATGCTTGCTTTGTGG[C/T]CTATCTCACTTTTCC | 26259 |
rs545839932 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013112 | GCCACGCATGGTGAC[A/G]CATGCCTGTAATCCC | 26259 |
rs545851920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941618 | AATGATTATTTTTGG[G/T]ATAGTTTGCTTGAGA | 26259 |
rs545860810 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031746 | CTTTAAGCAAAATGA[C/T]ATATAATGAAACTAA | 26259 |
rs545913300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950766 | TTAGAAAGGTTGATG[G/T]TCCAGATACTTGCGA | 26259 |
rs545969138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996387 | CATCACGAGTTGAAA[C/T]ATCTGTCTGGGAGAG | 26259 |
rs545992358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987481 | AAGTGCCGGCGGTGA[C/T]GCAGTCAGGACTGGG | 26259 |
rs546026603 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932254 | ATCCATTCTCCATAA[C/T]TGCCAAAAAATTAGT | 26259 |
rs546069101 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020508 | CTCATGTCTCTTATA[A/C]CCCCATTCGCAGTTT | 26259 |
rs546086534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981650 | ACAGAGTCTCACTCC[A/G]TCACCCAGGCTGGAG | 26259 |
rs546131532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980593 | CCGCAGTATGATAAC[A/G]CTTGACCTTTCAAAT | 26259 |
rs546165691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001604 | GCAGCCTCAGTTTTC[A/G]CTCCGTAAGATAGAT | 26259 |
rs546197195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982706 | AAGGATATTTTATTG[C/T]ATAAAGTTCTGTTGG | 26259 |
rs546219714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972174 | ATAAATTCACAGTAG[C/T]TGTTCTATTTTATTA | 26259 |
rs546284340 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016098 | CATTTGGGTTGCTTC[C/T]ACCTTTTGACTATTA | 26259 |
rs546311469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937656 | TGTTGGGGGCAAAAG[C/T]TAGTGGCTCAGGAGC | 26259 |
rs546333211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116974878 | TCTGGAACATTTTAT[A/G]GGACCCAAAAGTAAG | 26259 |
rs546408687 | in-del | -/A | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031713 | GCGAGACTTCGTCTC[-/A]AAAAAAAGAAATGGC | 26259 |
rs546424581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935238 | TTGACAGCAAAATAA[A/G]TAAGTAATTCTAGAA | 26259 |
rs546434146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960417 | GACGTAGAGGCTTTT[A/G]TATTTTACCTCCTGA | 26259 |
rs546445716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998487 | AGGCTGGTTTTTCTT[C/T]CCTGATGGTTTATGT | 26259 |
rs546449732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005122 | TATGAAGAGATCTCT[A/G]TGGAACCATCTTCTG | 26259 |
rs546460950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010992 | GGGAGTCGGATTTTC[C/G]CGGTATAGGGGCCTG | 26259 |
rs546476226 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029900 | ACAGGTGTAAGTCAC[C/T]GTACCCAGCCCAAAA | 26259 |
rs546485332 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921720 | TATCATGTGCTCACT[A/G]TAGAAATATTTAGGA | 26259 |
rs546509166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011262 | AGGTGGCGGGCTGCT[C/T]GGAGGCGGGTGTCAG | 26259 |
rs546524230 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016766 | TTTATAGTTTTGGCT[C/T]TTACACTGAGGTCTG | 26259 |
rs546540249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922668 | ATTAGCACATAGGAA[C/T]ACAAATCAGCCTCCC | 26259 |
rs546574658 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023167 | GAAAATTGACGTGTG[C/T]GCGCATGCTTGCATA | 26259 |
rs546574875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027946 | CTGGTCTCAGGCGAA[C/T]GCCTCCTGCACAGAC | 26259 |
rs546602592 | snp | A/G | | | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978353 | GCATTTCAGAGTGGT[A/G]ATGTGTGGACTTAAT | 26259 |
rs546635339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923502 | GCTGAGAGCTATTCA[A/G]CTACTGCAAAATTAT | 26259 |
rs546663228 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015225 | GGAAAAACATGGGAA[A/C]CTCTTCCCCTGTACA | 26259 |
rs546682319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015976 | CACTTAGCATGTTTT[C/T]AAGATAAACCCAAGT | 26259 |
rs546686364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931533 | CTATTTATTTGTATC[A/G]TCCGTTTTCTCCTTA | 26259 |
rs546719096 | in-del | -/T | 0.00914312 | 0.0669923 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978812 | AGTATACCAATTGTG[-/T]TTTTTTTTCCAAAAC | 26259 |
rs546730221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924615 | CTGCACACTAGTAGC[A/G]AGTAGTGTTTTTAAC | 26259 |
rs546734045 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958036 | ACTCTGCATAATCAT[C/T]ATTGACTCTGACTCT | 26259 |
rs546737174 | snp | C/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983925 | AGGCTAACAGGCTCA[C/G]AGCTGTTAAGCAGCT | 26259 |
rs546749558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952254 | GCCACCTGGGTTTGT[A/G]TAAGAACACTCTGTG | 26259 |
rs546749657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944506 | CACTCTTCATTAGAA[A/G]TGAGACTCAACTTTT | 26259 |
rs546761121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958792 | TATGGGGCAGAGATG[C/T]TGCCCTCCTCACTCC | 26259 |
rs546803007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919057 | AATAGAACAATTACA[A/G]CAGTATACTATAATG | 26259 |
rs546832227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116911919 | AAGAATCTCCTGGGC[A/G]CTTTCATTAGGATAG | 26259 |
rs546839132 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003216 | GGCCAGCATAGCAGT[A/C]GCCTGTAAGGGGTAG | 26259 |
rs546854746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961143 | TGGGATTACAGGCAC[A/G]CACCACCACACCTGG | 26259 |
rs546864390 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116918532 | GACTTTATTCACAGA[C/T]AGGCTTTCCTCTTGG | 26259 |
rs546909399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953085 | TAATATTTTGTTAAA[C/T]GTATACTGTTTTATA | 26259 |
rs546915986 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019646 | AAACCGAACATATGT[-/A]TGGGAGTGTATATAA | 26259 |
rs546956841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916637 | GCATGGTGGCACATG[C/T]CTGTACTCCCAGCTG | 26259 |
rs546959503 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013135 | GTAATCCCAGCTACT[C/T]GGAGGCTGAGGCAGG | 26259 |
rs546967629 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975771 | ACAATTGAGAGGCCT[A/G]CACAATAAATGAGCA | 26259 |
rs546969357 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011664 | GGCTCCAAGCTCCTC[C/T]CCTAGGATCTCCACA | 26259 |
rs546979437 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966022 | CCTGCTTCAGCCTCC[C/G]AAAGTGCTAGCATTA | 26259 |
rs547022831 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960624 | TGTACATTCTGGGTG[-/T]TTTCACTCATCATTA | 26259 |
rs547024638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933190 | AGCTAAATGAGGCCA[A/G]TTCCTGGATTTCAGC | 26259 |
rs547040105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920779 | ATTTGTGACCAACAG[A/G]CCCCCCAAATTCTAT | 26259 |
rs547059314 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922108 | GTGTTGGGATTACAG[A/T]TATGAGCCACTGTGC | 26259 |
rs547063928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912764 | CACCGCGCCCGGCCG[A/C]GAATAATTCTTTTAA | 26259 |
rs547092788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953509 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 26259 |
rs547098485 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962099 | GATGATCCCATTGAT[A/T]AAAATAAGGAATTCA | 26259 |
rs547137838 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032090 | CTGGGCACTTCCGTA[A/C]AGCGTCATTTACTAT | 26259 |
rs547151577 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116911749 | CCTGCTCTTGAAGGC[C/T]ACCTAAACTTTGAAC | 26259 |
rs547155397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941017 | TGATCGCTGTCTTCA[C/G]CTATTTGAGGGACTG | 26259 |
rs547157359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948767 | ATTTAATTTTTTATT[G/T]TTTTAGAGATAGGTT | 26259 |
rs547220565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947995 | GGTTCTGTGCTGTGC[C/G]TGCTCGACTTCAGGA | 26259 |
rs547236254 | snp | C/G | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010803 | TATTAAAAACAGTAA[C/G]CTAAGGGATGAATCA | 26259 |
rs547255703 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953772 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAGACAA | 26259 |
rs547269618 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005164 | ATGGAGCAGTTCCTT[C/T]GTACATACCAGCAGC | 26259 |
rs547295024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941726 | TTTCTGTGTGACTTA[C/T]GTCTTTTTTATACCT | 26259 |
rs547304031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116989088 | CACAGAAGAAACTAT[C/T]AACAGTTTTTAGGTA | 26259 |
rs547327054 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962618 | TCTTTTTCTGAACGT[G/T]CCTTACTTTTCTGAT | 26259 |
rs547386991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999193 | CCACATCTGAGCGGT[C/T]GCATCCCAAACTAAG | 26259 |
rs547392413 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912380 | TTTTTGGTAGAGACA[A/G]GGTCTCCCTGTATTG | 26259 |
rs547464609 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028443 | GGCCTCAGCTCCCTC[A/G]GGACGCCTCAGGGAT | 26259 |
rs547471643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000505 | TGAGCACTGGCCCCA[C/G]CCCCGGAGCTTCCGA | 26259 |
rs547493292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913438 | ACCAGAAGCCTTATA[A/G]ATAAGTCAGTTAACA | 26259 |
rs547536877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006459 | GCTCTTTCCTTCACA[A/G]TTTGCCTGGAAAGCC | 26259 |
rs547541539 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024718 | GACCAGGATGTGACA[A/C]CCCACCTGCCCACAG | 26259 |
rs547612565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991720 | GTTTATATTTGTTTG[C/T]ACCTGATACAAAACT | 26259 |
rs547626397 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015814 | CACCCCAAATAGAAA[-/C]CCCAAATCCATTAGC | 26259 |
rs547626700 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029000 | TCAGAATATCAAAGC[A/G]AAAACTGATAGAACT | 26259 |
rs547639851 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116958025 | CAGCTACAATAACTC[C/T]GCATAATCATCATTG | 26259 |
rs547643867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986373 | AAAACTTCCATAGTA[C/T]TTACTATTTAGTCTG | 26259 |
rs547653745 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030217 | AACTACACAGGGGAA[C/T]GGAGCAGATAGAGCT | 26259 |
rs547694024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926748 | ACTCTTTTTTTCCTC[C/T]AGAGATCCCTTTTGG | 26259 |
rs547698443 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932760 | GATGGTCTCCATCTC[-/TT]GACCTCGTGATCCAC | 26259 |
rs547699457 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029214 | ACAAAGATTCACACC[A/G]TACAGGCCAAATTAT | 26259 |
rs547762329 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994806 | TGGATGCTAGATTGC[A/T]CCTGGTGTTTTGCTA | 26259 |
rs547771886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946758 | CCAGTCCCTCTTGCC[C/T]GTGTGCCTGGGTAGG | 26259 |
rs547843531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992388 | AAAAATAGCAACTAT[A/G]TATTTTTGCCCTTTT | 26259 |
rs547854966 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931458 | TTGCATTTCACTCAC[-/T]TTTGAGTAGTATGGA | 26259 |
rs547858063 | snp | A/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986481 | AAAATACAAAAAATT[A/T]GCCGGGCGTGGTGGT | 26259 |
rs547938811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022427 | TAGGAGGCTGAGGTG[A/G]GTAGATCCCTTGGCC | 26259 |
rs547950465 | snp | C/T | 0.000461201 | 0.0151785 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988787 | TTTACGCCCACGGCC[C/T]GCCTGTCACATGTCT | 26259 |
rs547957521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923548 | GTTTTGAGACAGAGT[C/T]TCGCTCGCTCTGTCA | 26259 |
rs547973745 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930075 | TACATGCCACATTAT[A/G]TATCATTTATCTGTT | 26259 |
rs547988261 | snp | C/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909513 | GGGCACCTGTAGTCC[C/T]AGCTACTCAGGAGGC | 26259 |
rs547994974 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955955 | CCATTAAGCCATTAG[C/G]TCACCAGAAGCTTTT | 26259 |
rs548018449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976616 | ATGCACCACCACACC[A/G]GCTAATTTTTTTTTT | 26259 |
rs548027874 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021606 | TTGCCTCTAACTGCT[A/G]TTACAAATGGGACAT | 26259 |
rs548031988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917459 | TACCTTCTTACACTT[C/T]CTCCCTGCCCCCGTT | 26259 |
rs548057266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929791 | TCTGAACTTATTTCT[C/G]TCATCTAACTGAAAT | 26259 |
rs548085138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015328 | TGTTTTTGTGTTTTG[C/T]CCATAGGTTTTGCTG | 26259 |
rs548093182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970103 | GGACTCCATCTGCTC[C/T]GTGCTTGCCTGCCTT | 26259 |
rs548153288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977048 | CCTTGTGGCAAAACC[A/G]TCTATTTGTTGGGGG | 26259 |
rs548188570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979198 | ATCGAGTAATCTTTA[C/T]AAAAGCTAACATAAA | 26259 |
rs548259668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972258 | GATAGTTTAGACTGG[A/G]GAAATAAATTGCCCA | 26259 |
rs548324866 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014056 | TTCCAGTAACCTCAA[A/T]AATGTAAATATTAAA | 26259 |
rs548378052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964162 | CACTGTCTGGCTGCT[A/G]AAGGCAAGATTTAAT | 26259 |
rs548398641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013508 | CGGGGAGTGATGCAC[A/G]TCGGCATTAGGGCTG | 26259 |
rs548404052 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929283 | TCTGTCACCGAGGCT[A/G]GAGTGCAGTGGCGCG | 26259 |
rs548433577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995217 | ATCGGCAGCGTACGC[A/G]GACATGCTCCCCTTC | 26259 |
rs548433687 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002366 | AAGCGGCTCAGGCTG[C/G]TTCTCCCTTTGTGCT | 26259 |
rs548439295 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979793 | AAAAAAAAAAAAAAA[A/C]AAACACTTGCTTCTT | 26259 |
rs548446482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936876 | GAATAAGATGGGAAG[C/G]CTTTGGAGTGCTTTG | 26259 |
rs548461161 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991023 | TAGTCCTGTAAGCTG[C/G]TGTTTTCGCTGGTGT | 26259 |
rs548472545 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951128 | CTCGGGGTCTGTTCA[A/G]CATTACAGATTATGC | 26259 |
rs548488682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966900 | ATTTTTGTATTTTTA[C/G]TAGAGACGGGGTTTC | 26259 |
rs548521684 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029750 | GAGTAGCTGGGATTA[C/T]AGGCGTCCGCTACCA | 26259 |
rs548541039 | snp | A/G | 1.65963e-05 | 0.0028806 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928080 | TACGAATTGGCAATC[A/G]ATATATTTCAGTATC | 26259 |
rs548558756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026408 | AGGCCTCCACCAAGC[C/T]TGCCCTCCCTTCCCG | 26259 |
rs548559161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020201 | TAATCGTGTCACCTA[C/T]GTCATTCCAGTTCAT | 26259 |
rs548604874 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934553 | AGGAGAAAAGTAAGT[C/G]TGCCATTATATTACA | 26259 |
rs548620639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008899 | TGAGGTCAGGAGATC[C/G]AGACCAGCCTGGCCA | 26259 |
rs548644641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960611 | AATGCACATCAGTGT[A/G]TACATTCTGGGTGTT | 26259 |
rs548646561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025772 | TGAAATTCCCGGAAG[C/G]ATTGCCTTTGAGGAA | 26259 |
rs548652649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914732 | AATACAAAATTAGCC[A/G]GGCATGGTGGTGGGT | 26259 |
rs548655003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969120 | ATCAAGCTTGTCAGT[C/G]TTGTCCTTTGGGGTT | 26259 |
rs548706702 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021989 | TCGGATATGTAGTTT[C/T]CTTTGATCATGCTCT | 26259 |
rs548714247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988353 | CATGGAACATGGTTT[C/T]CCCTCCTTCACTTCC | 26259 |
rs548717250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957020 | ACCTTGCTTTTAGCT[A/G]TGTTGTCCTCTGCTT | 26259 |
rs548718331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968429 | CTTGGCTTTTTTCTC[C/T]AAATAGCATATCTTA | 26259 |
rs548755955 | snp | C/T | | | synonymous-codon, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985234 | TTGGGATTTAAGGAC[C/T]GGAAAGTACCCTGTT | 26259 |
rs548786845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915584 | CTTCTCTTCCACCCA[A/G]GGGTAACCACTCACC | 26259 |
rs548800320 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116999618 | AGTGCCCCTCCTCAC[A/G]GTCCACTTCAGGTTT | 26259 |
rs548807967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014218 | CCATTCTGCTGTTGA[C/G]CCTATCCAGTGAATC | 26259 |
rs548819268 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991890 | TGGAGAATATTCTTA[C/G]ACCGTATGATGCCCA | 26259 |
rs548831686 | snp | G/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983295 | CAGCATATTTTTCTC[G/T]TCTGAGTCAGGATGG | 26259 |
rs548848184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922820 | TGTGTGTGTTTTTTT[C/T]CCCTTGACTAGGAAA | 26259 |
rs548855492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953537 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 26259 |
rs548890737 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949906 | GGTGAGAAGCACATG[G/T]TGTAGAGCGGATCTG | 26259 |
rs548893034 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116940494 | GAAGGATGGTGGGCT[-/T]TTTTTTTTTTTTCCT | 26259 |
rs548894608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955741 | GCTTAGACTGTTCTC[A/G]TCTTCCTTCTCCCCA | 26259 |
rs548947438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011505 | TGAGAACTGAACTCC[C/T]CAGTGTGTGTGTGGG | 26259 |
rs548966106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017005 | TATGTCTGTGTTCTG[A/G]CACTACCACGCTGTA | 26259 |
rs548998181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946786 | AGGTCCATGTGATGC[A/G]CACAGGCAGAAAGGT | 26259 |
rs549044158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023906 | AGCAGGTAAAGTGGG[C/T]AGCCACTGTCCTTGG | 26259 |
rs549061116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959608 | TTATGAAGAAGAAAG[G/T]TTGTTTTTAGCTGTA | 26259 |
rs549091427 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910150 | GAGTAAGTTCTTTAG[C/T]GGTGATTTGTGAGAT | 26259 |
rs549113532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919139 | GGAAAGCAAAACCGC[A/G]GATAAGGGGGGACGA | 26259 |
rs549130018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937725 | AGAGCTGTCTCTATG[C/T]GGTGTGTCCTCCCAC | 26259 |
rs549255574 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001870 | ACATTTCTTACCCTT[-/A]ACACCAGCACTGAGA | 26259 |
rs549278367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005821 | TTCAGAAGAGCCAAG[A/G]GCCACATATGTGAGG | 26259 |
rs549301478 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944722 | ACAAAATGCTAATAG[-/T]TAAAATGGCCATTTC | 26259 |
rs549311348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951662 | TCATTGATGGAGAGC[A/G]GAATCTCTTCTTCTC | 26259 |
rs549337732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002926 | CCTTGCATTTTTGTA[A/G]TTCAATTCCACGTTT | 26259 |
rs549355166 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914559 | GCCTAGGTGACAGAG[C/G]GAAACCCTGTCTCAA | 26259 |
rs549407487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013374 | TTGTAAAGATGGGAG[C/T]GGAGAGAAAAGTGAG | 26259 |
rs549453548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997695 | CACCAGGTATATTCA[A/G]GCCTGCAGGAGCACC | 26259 |
rs549491973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000526 | GAGCTTCCGACTCAG[C/T]GGGTCGAGGGTGGGG | 26259 |
rs549512250 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989378 | TAAGCAATGCTACAA[C/T]GCATATTGCAGCTTG | 26259 |
rs549524683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955255 | AAGGATATGCAGCAG[C/T]GCAGAAAAGACCTGC | 26259 |
rs549566484 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032733 | AAGCACAACTCCCTG[C/T]GCCGGCTGAACGCTA | 26259 |
rs549588837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989994 | TCCCGTTATTCCTCC[C/T]ACCCATAGTTGGATT | 26259 |
rs549590051 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019017 | CAAGTTCCCATTATG[C/G]ACTAAGGTTAGAGTT | 26259 |
rs549593584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941804 | GTATGCTATTTAAAT[G/T]TCTTTACTCTGTTTT | 26259 |
rs549667113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935667 | GCTAGATGAAACAAG[A/T]ATGGCAAATGAACAT | 26259 |
rs549675849 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942480 | CCTGGGTTCAAGTGA[G/T]TCTCCTGCCTCAGCC | 26259 |
rs549718209 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990629 | TTTTTATAAATGTTT[C/T]CTCCTTGACTTATCT | 26259 |
rs549826826 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963786 | ACTATGAACCCCCTT[A/C/G]AAATCATTGGCCTAT | 26259 |
rs549851365 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914707 | AAGGAGAAACTCTGT[C/G]TCTACTAAAAATACA | 26259 |
rs549853636 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992622 | GCATACCCATAGCTT[A/G]GCTCCCACTTATAAG | 26259 |
rs549857421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994218 | CTGGTATAAAAGTAG[A/C]TGGTACTGGTGTAAA | 26259 |
rs549921489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019466 | GCTGTGCTACCTGTT[A/T]CCCAGCGTTGAGTAT | 26259 |
rs549965235 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020741 | AGCTGAGCCTGGCGC[C/T]TGCCAGCAGCCTCCC | 26259 |
rs549972651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977253 | GAAAGGGAATTAATT[C/G]ATAGTATAATTTTAA | 26259 |
rs549993247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024853 | GAGCACTTAGGACTG[A/G]AGGGGTTCAGGCTCC | 26259 |
rs550008794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018778 | GAGCCATCCATGCTG[G/T]TATCTAAATACAATA | 26259 |
rs550033994 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984971 | CTCCAGCCTGGGCGA[A/C]GAGTGAGGCACTGTT | 26259 |
rs550063927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012891 | TGTTTTCATTAAAGT[A/G]GGGAATCAGTTTTAA | 26259 |
rs550076747 | in-del | -/T | 0.0322621 | 0.122842 | intron-variant | FBXW8 | GRCh38.p7 | 12:116918966 | CTGTATATGCCATGT[-/T]TTTTTTTTCCTATAT | 26259 |
rs550095724 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969315 | TGCTGAGCTTGTTTC[A/C]TTGGTCTGATTCGGG | 26259 |
rs550112890 | in-del | -/A | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030844 | ATCACACTGACAGGG[-/A]AAGGATAAATGCTCC | 26259 |
rs550163042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940192 | ATCCGTGTCAGCCTG[C/G]GGGGTGGGCTCCAGT | 26259 |
rs550257820 | snp | A/G | | | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978060 | CAGATTCTTTTACTT[A/G]TCAATCTAAAATGCA | 26259 |
rs550346619 | in-del | -/TGAG | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992746 | ATTCCTTTTTATGGT[-/TGAG]TATTATTCCATGGTG | 26259 |
rs550351476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977952 | TACTAAATATATTCA[A/G]TCTTACTTCCTCTTC | 26259 |
rs550367945 | in-del | -/AAAG | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982409 | GACTTTGCCTGTGAT[-/AAAG]AATCAACTCATCAAG | 26259 |
rs550386236 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932968 | GATATTTTTTGATGC[A/G]GAGTGTGTGTCTTTA | 26259 |
rs550386707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015391 | ACTCCGTTCTGGCCA[C/G]AATCAGAACGTCCTC | 26259 |
rs550390088 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027676 | TGTACTGAGCACCCA[C/G]CATCTGATGCAGGAC | 26259 |
rs550398366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025251 | TACTCAGGAGACTGA[A/G]GAGCTCTCAAGGCCA | 26259 |
rs550415531 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910246 | CCTTCCCACCCTCCC[C/G]TCGTCCCCCTCCCCT | 26259 |
rs550423472 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018809 | GGAAAACAGATGGCA[A/C]ACTTTGAACTTCTGG | 26259 |
rs550434482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933718 | CAGGAGTTTTATGGA[C/G]CTCTTACATGAGAAT | 26259 |
rs550533520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970542 | GGTGAACAGTAGGAC[C/G]ATGTTTTAGTTAGAC | 26259 |
rs550551458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023106 | CACTTGGTAGCTAAG[C/G]TAGGTATAGAATTGT | 26259 |
rs550560073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936967 | GAGAATCGGTTGTTG[A/G]GGGACAAGGACAGCA | 26259 |
rs550605144 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032042 | AGCGCCTCCTTCCAC[C/T]ACGCAGGTCAAACAC | 26259 |
rs550637672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022471 | CCAGCCTGAGCAACA[C/T]AGCAAAACCGTCTCT | 26259 |
rs550661659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021358 | TATAAGACATTAGCC[A/C]TTTTTGTTGCAAACA | 26259 |
rs550724560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958664 | GCACGGTGCCATAAC[A/G]TGCTAGGGAGAGGCA | 26259 |
rs550731363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917503 | TTGGCACTTTCATTA[G/T]TGCACCCTGTTGTAT | 26259 |
rs550750826 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916553 | TTAGATTTTTTTTTT[A/T]AATTGGGAATATGTA | 26259 |
rs550753808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966928 | TTCACCATGTTGGCC[A/C]GGCTAAGAATCTGCT | 26259 |
rs550814098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923429 | CTTAACATTGAAGGA[A/G]TACTAATATTTTGAA | 26259 |
rs550895917 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017866 | GCCAATAGGAAGCAC[A/G]CCCTGAGTTGTGACC | 26259 |
rs550952712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972372 | TTTAATTTCCCTTTC[A/T]CTATGTGCAGTTTTG | 26259 |
rs550975758 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023921 | CAGCCACTGTCCTTG[A/G]CCTGCGTCTTTCTTG | 26259 |
rs550976031 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116999937 | TCTCATTGAGCATCA[C/G]AGCTCTGGCCCTGAG | 26259 |
rs550982643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951379 | TTTCATTTGAGACAG[C/T]GGTGTTTGTGGTTAC | 26259 |
rs550990044 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951521 | CGTGTTTCTCTTATT[A/C]TTCTTTTTTCCTTCC | 26259 |
rs551006891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926007 | CTAGGGTGATGCCAA[A/G]ATACGGGCATTGTCT | 26259 |
rs551065011 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921600 | ATATACTTGCTAACA[C/G]CACCTCCCTCCCCCT | 26259 |
rs551097106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014701 | TCCAAAGCTGTTCAA[C/T]TTCTATGCTGTTTTT | 26259 |
rs551116273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017807 | GCTTCAGCTTGCCAT[C/T]AGCTACGGTGTTCCT | 26259 |
rs551121017 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955149 | AAACTCCCCTTCGGC[A/G]ATTCCACACTCTCTG | 26259 |
rs551153606 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991321 | TTTCCATCTGATTGT[A/G]CTTAATGGATTTTCT | 26259 |
rs551184923 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954846 | TGTACATAGTGAGAG[C/G]CCGTGCCTCCTGCCC | 26259 |
rs551187912 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973025 | TGAAGAATGATGACA[A/G]CATGTCACAAGGACA | 26259 |
rs551206574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912314 | TCCCTCAGCATCCCG[C/T]GTAGCTGGGACTACA | 26259 |
rs551236578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008940 | GGTGTGGTGGCGGGC[A/G]CCTGTAGTCCCACCT | 26259 |
rs551237404 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025927 | GAAGGCCTTCCCCAG[A/C]GGTGTGGCCCTGTCC | 26259 |
rs551254118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943385 | GTTATTTTTGTTGTT[A/G]CTGCTGTTTGTTTAG | 26259 |
rs551263849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999893 | AAAACAGTCCTACTT[A/G]ACAGAAGCAGCCTTA | 26259 |
rs551273150 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031520 | GGAGCTCAAGACCAG[C/T]CTGGCCAACATGGCA | 26259 |
rs551319363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018444 | AGCGTCGAGTATTTG[G/T]TTTGAGTGCTGAGCT | 26259 |
rs551322448 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975208 | CAAGAATCACCAGCG[A/G]ATGTTAAAATCAATG | 26259 |
rs551323039 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116945573 | AAAGAATAGCCTGCA[A/G]GGACATGGGAATCCA | 26259 |
rs551354621 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116910956 | CAGCGGCTTCCGGCC[G/T]CGGCGGACACTTCCC | 26259 |
rs551362114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977008 | AGGGGAGGGAGACCC[A/G]AGAGCCCCACCCCAG | 26259 |
rs551364904 | in-del | -/GAGA | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001983 | ACCTACGGACGTGCT[-/GAGA]GAGAGAGATTGGCCG | 26259 |
rs551383778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011525 | GTGTGTGTGGGGCAC[G/T]CACTGGGCTAGTTCT | 26259 |
rs551386225 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940268 | ATCTTTTTTTTTTTT[A/T]AAATAATTAAGACAC | 26259 |
rs551402527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992641 | CCCACTTATAAGTGA[A/G]AACATGCTGTATTTA | 26259 |
rs551411516 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912724 | CGCCTCGGCCTCCCT[A/G]AGTGCTGGGATTACA | 26259 |
rs551461854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004264 | CCTACTTTTTATCCT[C/G]TCCCTCTTTTATCTG | 26259 |
rs551493335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969924 | TGTTTCCGATTGTCA[A/G]CACTGGCCATCCTCC | 26259 |
rs551524493 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005285 | CTGGCATCGTGTACC[A/G]ATCAGTGAGCCTCCA | 26259 |
rs551527840 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947696 | GTGAGCCAAGATTGC[A/G]CCATTGCACTCCAGC | 26259 |
rs551530726 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931909 | GGAAATGGTGAGAGT[G/T]TGCATCCTTGTCTTA | 26259 |
rs551575046 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922258 | CAACCAGTTTTTTTC[G/T]TCTCAAAGAAGACAC | 26259 |
rs551581471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946306 | TCTGTCCCTACTCAC[C/T]TCCTAACCTGATTAG | 26259 |
rs551590096 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975336 | TGGAAAGTCCAAGAT[C/T]AGGGCACTGGCAGAT | 26259 |
rs551597821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998268 | TTGGAGAGGGCTGGC[A/C]CCAAGTCTTAAATGT | 26259 |
rs551604486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993391 | ACAGGTGTGGGCCAC[C/T]GCACCCGGCCTGTTT | 26259 |
rs551633296 | in-del | -/TCTTA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021281 | CTGTGAATTGCTTTT[-/TCTTA]TCTTTTCTGTCGATT | 26259 |
rs551640891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005945 | CCACTCAGCCCAGCA[C/T]AGCACCTCCTAACCT | 26259 |
rs551713565 | snp | C/T | 0.000337866 | 0.012993 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945544 | GTGGGCAGTGGCCAA[C/T]ATCATTACCTGTGAA | 26259 |
rs551722300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938807 | TTGAACACATAATTT[A/G]AAAGATTGCTTCCCC | 26259 |
rs551729558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997834 | GTTTTGTTTTTTTGA[A/G]AGATGGAATCTCATT | 26259 |
rs551753820 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001781 | CGATGGTTATCATCT[C/T]TTCGCTGGACTCACT | 26259 |
rs551754618 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976447 | TTTTGTTTCCAAAGG[A/T]TCCTTTTTTTTTTTT | 26259 |
rs551756675 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942930 | CTACAGGTGCGTGCC[A/T]CCATGCCTGGATAAT | 26259 |
rs551801664 | snp | A/G | 1.6477e-05 | 0.00287024 | stop-gained, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024237 | GCAGATGGATGACTG[A/G]AAGATCGTCAGTGGA | 26259 |
rs551835501 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030779 | GTCATCTTCAAGCAC[A/G]CCAACTTCAGGCAGT | 26259 |
rs551853547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990575 | GTATAGAGAGGTGAT[A/G]GTTATATTCAGTACC | 26259 |
rs551901874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023969 | CCATTCAGATGAGAC[C/T]GTGTGGGTCCTCCCT | 26259 |
rs551904576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026903 | GTTCCAAGATTTTCC[A/G]AACGTGCTTTCACCA | 26259 |
rs551938315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995835 | AAAAGTCAGTGTGAA[C/T]GCTGTTAATGTAGCC | 26259 |
rs551963101 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937449 | CAGAGGACCGGGAAG[A/G]AGTTCCCTGCCAGGC | 26259 |
rs551994514 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026607 | CTCCTGTGCACCCCT[C/T]CCAGCCCACAGCACC | 26259 |
rs551995630 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929304 | CAGTGGCGCGATCTC[C/G]GCTTCCTGCAACCTC | 26259 |
rs551997020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991592 | ATTAGGCTGGTGTGA[A/G]ACTATTAGCAGTAGA | 26259 |
rs552031356 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012185 | CCTCATTATGTACGC[A/G]CTGCCAGGGAGGTGT | 26259 |
rs552059945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929219 | CTCGTCTTTTTGGCC[A/G]AGAGTGTGTGATTGA | 26259 |
rs552077308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987775 | TATTACATCCCCATG[A/G]TTCAGAATTTAAAAG | 26259 |
rs552082170 | snp | A/C | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909647 | AACAAAACAAACCAA[A/C]CAAACAAACAAACAA | 26259 |
rs552123098 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927742 | TGGAAGATAGCACCC[C/G]TGCTGCTTTGTGAAG | 26259 |
rs552124082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943242 | CTGCCTTTTCCCCTG[C/T]GTATGGGCCCTGCTT | 26259 |
rs552132057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984196 | AAATGCTAAGTACAG[A/G]AAAGGTTATCTGACT | 26259 |
rs552145228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985474 | GTAAGCACGTACTAA[C/T]GGTGTTGGTAACTCC | 26259 |
rs552160533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949853 | AGAGGGAGAGTCTCC[A/G]TGATTCTGTTCCCAA | 26259 |
rs552186733 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953153 | TGTCCCCTGCCACCT[A/T]TATATGATGTTATAT | 26259 |
rs552221036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978970 | TTGATGGAAGCTTAA[C/T]TGCAATTTTGGCTTT | 26259 |
rs552223811 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956794 | CTAACATGGTGAAAC[C/G]CTGTCTCTACTAAAA | 26259 |
rs552245609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942559 | TTTTATATTTTTAGT[C/T]GAGATGGGGTTTCAC | 26259 |
rs552282100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978064 | TTCTTTTACTTGTCA[A/G]TCTAAAATGCAGATT | 26259 |
rs552282339 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014723 | GCTGTTTTTGGTCTG[C/T]GCATGTGCCACATGG | 26259 |
rs552283984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986262 | TTCACCTCCAGGAGC[A/G]TCTGCACTTTGAGTA | 26259 |
rs552350451 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001717 | GGCCTGTTGGGAGCA[C/G/T]GAAGGAGGGTGTAAG | 26259 |
rs552359030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970712 | CAGTAAACAACTACC[C/T]CCCTGCCCCCAACAT | 26259 |
rs552406050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019612 | AAGAAATAGATGAAA[C/G]TATTATTTTTTAATT | 26259 |
rs552409152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980158 | ATGTACCCAGGGATG[A/G]GAGAAAGCTGGTTTC | 26259 |
rs552460736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021437 | AGGAAAAAGTTAAAC[C/G]CTTTTTTCACCTTCC | 26259 |
rs552485701 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032272 | CTGGACAGGATGCCC[C/T]CCCATCACAGGGCAC | 26259 |
rs552555113 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030143 | AACCTTCACGTCATG[A/G]AGGTTCTGGAAGGTT | 26259 |
rs552578105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940893 | GACACTTTAGATGTA[C/T]AAATGTTTTAGGGTG | 26259 |
rs552579400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933837 | TTTCATTTGTTTCTT[C/G]GGGTGTTTTTATTTT | 26259 |
rs552657210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010057 | ACCTGATTTCCCTGC[A/G]TTTTCCTTGTGGCCT | 26259 |
rs552664046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015448 | ACAGTAGTTGGCAGT[C/T]AAGGGCTGTATTAAA | 26259 |
rs552715416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934398 | TTGGACAGTTCATTG[A/G]ACAGGTTTGTAATCT | 26259 |
rs552717499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025680 | GTGCCTGTTGAGGGC[A/G]CCTCGGCCCTTTTTC | 26259 |
rs552722108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922173 | TAAGAATATATATTT[C/T]GAGACAAATTGTGGA | 26259 |
rs552732596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003649 | TCACAAGTGTTTTCC[A/G]TGTTTCTTTCTTACA | 26259 |
rs552737409 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003694 | TCCTTATCCTTGAAA[C/G]GTAGTTTTGCTAGTC | 26259 |
rs552741142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971340 | ATTTCTGCCTGGGCA[A/G]CAGAGCAAGACCCAG | 26259 |
rs552756408 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008683 | TTATTATTAACTTCT[C/T]AATACTAAAGTAAAA | 26259 |
rs552764599 | snp | C/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979583 | TTCTTTTGTCTGCAT[C/G]CTTTTCCTGTTTGTT | 26259 |
rs552804954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917709 | CATGAAAACGCAGGA[C/T]TCACTGGGCATGGTG | 26259 |
rs552807382 | in-del | -/TTTA | 0.00398564 | 0.0444627 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018742 | GGCCGCATCTTTTGG[-/TTTA]TTTGTTTATTTTGTT | 26259 |
rs552836307 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007198 | GATACATCAGAATCA[C/T]TGACAAAATTGCAAG | 26259 |
rs552837772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967138 | CTCGTGGGGGGTCCT[A/G]CTCTGTATACTTCTC | 26259 |
rs552850246 | snp | C/G/T | 0.000588502 | 0.0171439 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928011 | ACTTCTTTCTTTTTT[C/G/T]TTTCCCCTCAGAATG | 26259 |
rs552853488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914690 | AGACCAGCCTAACCA[A/G]CAAGGAGAAACTCTG | 26259 |
rs552869700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997908 | ACAACCTCTGCCTCT[C/T]GGGTTCAAGCAATTC | 26259 |
rs552916062 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021676 | TATAAATTTATATTT[A/G]ACTCTGTGTTACTGA | 26259 |
rs552941569 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909574 | GCGGAGCTTCCAGCG[A/C]GCCGAGATCGCGCCA | 26259 |
rs552965388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015033 | TGGGGCACAGCCACA[A/G]GAAAGAGAAAAAAAC | 26259 |
rs552967837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957239 | GTAATCTCAGCTACT[C/T]GGGTGGCTGAGGCAC | 26259 |
rs552988921 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032909 | GCTTCCCACCACACG[C/T]GTTAGATGGCAGACA | 26259 |
rs553029738 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117004645 | AACCTGAGGCAGACA[C/T]GTTTCTGGGTAAGCT | 26259 |
rs553038535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923649 | CTGGCTCAGCCTCTC[A/G]AGTAGCTGGGACTAC | 26259 |
rs553046681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022519 | AATTAGCCTGGTGTG[G/T]TAGCACGTGCTTGTA | 26259 |
rs553146559 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963372 | AACACTTTTGGAGGC[C/T]GACGTGGGTGGATCA | 26259 |
rs553154459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996111 | TCTTAGCATCATTCT[A/G]TGTATTTGGACATAT | 26259 |
rs553157070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944844 | TTCTGTTAATTAAAT[A/G]TATACATATGTTTAA | 26259 |
rs553179747 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010532 | GCTGCTCACACTGCC[C/T]GGTTCTCACTCAACA | 26259 |
rs553221218 | snp | A/G | 0 | 0 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982057 | AATTAAAATGGAATA[A/G]CCACATTTAGTTATC | 26259 |
rs553222390 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951867 | ACACTCAAATACCCA[A/T]CATGTGAACAGGACC | 26259 |
rs553284576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981134 | TTATAGAGCATTCTT[G/T]TAATTCAGTTATTCA | 26259 |
rs553295787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945653 | GTACACTGAGCCTCC[C/T]CTTCAGCTGTTGGTG | 26259 |
rs553307294 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947099 | TGTCCTTGTTGGGCC[G/T]GGAGGTGGCAGAAGT | 26259 |
rs553388522 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987600 | ACAGCAGATCACTTG[G/T]ATATTTTTAACCTTT | 26259 |
rs553442014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947545 | TTGAGGTTAGGAGTT[C/T]CATGGCCAATATGGT | 26259 |
rs553451740 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995471 | CCGAGGAATCCATTA[G/T]TCTATCACTTCTTCT | 26259 |
rs553528357 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002459 | AGGGAACGTTGAGGG[G/T]GTCAGGGATCCATTT | 26259 |
rs553552195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935942 | GTTATTTATATAGAG[C/T]TGACTATGTATGTGC | 26259 |
rs553554049 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001703 | CTCTGTGGGGATGAG[G/T]CCTGTTGGGAGCATG | 26259 |
rs553571553 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027137 | CTGGAATGTACCAGG[C/T]TGTGGGGGCAGATGC | 26259 |
rs553608301 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031594 | TGGCGTGTGCCTGTA[A/C]TCACAACTACTCGGG | 26259 |
rs553622114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970319 | GAGGAAGCCTGGACG[A/G]GACAGCCAGCAGTCC | 26259 |
rs553649172 | in-del | -/TCTC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933926 | GGGGCTTGCTTTTTT[-/TCTC]TCTCTCCATCTCTCT | 26259 |
rs553679908 | in-del | -/CAAA | 0.00203252 | 0.031814 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909644 | AAAAACAAAACAAAC[-/CAAA]CAAACAAACAAACAA | 26259 |
rs553700905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929447 | GTCATGTTGGCCAGG[A/C]TGGTCTTGAACTCCT | 26259 |
rs553710002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932824 | GGCGTGAGCCACTGT[A/G]CCCAGCCGTTCTAAT | 26259 |
rs553718700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023367 | AGGGTCTCTTAAGCT[C/T]ATCTTTACATTTATT | 26259 |
rs553757335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027861 | ACCCCCACGTTGACC[A/G]CTAAGCCGGGGACTG | 26259 |
rs553771701 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951844 | TCACTCGTTGATAAA[C/T]GCATTTGACACTCAA | 26259 |
rs553780305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912432 | TGGGCCCAAGTGATC[C/T]TCCCAATTGAGAATC | 26259 |
rs553832341 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983555 | TTTATTTAGTGCTGA[A/G]TGATCCTTTATAGTA | 26259 |
rs553846586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931281 | GCTGTGTACATTGCT[A/G]TAGCTTTGTAGTATA | 26259 |
rs553848190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005356 | ACTGACACTGTACCT[C/G]GCATGTACTGCCCTT | 26259 |
rs553879072 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014234 | CCTATCCAGTGAATC[C/T]TTTATTTCAGATTTC | 26259 |
rs553896315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933348 | ATTGCTTTTTGCTCC[C/G]CTGCTTTGTAGAGAG | 26259 |
rs553907033 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938225 | AAAGAAAAGCACCCT[A/C]CTTTTATAGTTTGCT | 26259 |
rs553922200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919579 | ACTGAAGCTTATCAC[C/T]GATAAGCCCTTAGCT | 26259 |
rs553925998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000014 | TTTGAGACGGAGTCT[C/T]GCTGTCTCCCAGGCT | 26259 |
rs553957243 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956619 | GTTCAGTTTGCCTGT[C/T]GGCCCTTCAGTGGAA | 26259 |
rs553962321 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953621 | CTAAAAAATACAAAA[A/C]AATTATCCGGGCATG | 26259 |
rs553968865 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023959 | TGCTTTTAAACCATT[C/T]AGATGAGACCGTGTG | 26259 |
rs553978998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024978 | TAGGTAGGTTTACGC[C/T]AGTGGCACCTAACTG | 26259 |
rs554037360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927007 | TTGAGTGGTGAATTA[A/G]CAATTCGCTTGTAAG | 26259 |
rs554042096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011254 | CGGGCTGCAGGTGGC[A/G]GGCTGCTCGGAGGCG | 26259 |
rs554055364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920244 | ACTTACGAACCTTTT[A/G]AAATGATGCCTGTGT | 26259 |
rs554080208 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946607 | AATCCCCTCCCAGTC[G/T]AGAACCACTGTTCTG | 26259 |
rs554102804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938921 | AGTAGCCCCAGTCTG[G/T]GTGCATCCATGGGAT | 26259 |
rs554114226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017064 | TTCTAAAATAAGTAA[C/T]GTAACAGTAAACTTC | 26259 |
rs554137336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990678 | AGTAATACAGTTGTA[A/G]TGGATACATTTGAGA | 26259 |
rs554151452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026128 | TGTCATGTACCTCCC[A/G]CTGTCCGCTTCAGTC | 26259 |
rs554181409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116911437 | CAGTGATTTGGAGAG[C/T]AACTGTGTGCCACTA | 26259 |
rs554236505 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935843 | CAGCACATGCCAGGA[A/G]CTGAGCTGTGTCTAT | 26259 |
rs554243610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931986 | TTGGTTTTGTCACAT[A/G]TGGCCTTTATTGTGT | 26259 |
rs554245361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922569 | GCTCTTAGTAATTAT[A/C]TGTTCTTCTATTAAA | 26259 |
rs554278417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983593 | AAACTCAAAGCATTT[A/G]TAGTTTAAAGACAAA | 26259 |
rs554281291 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975855 | CCCCAGATTGGAGTC[C/G]ATGAAGGAGACATGG | 26259 |
rs554287271 | in-del | -/GAGGT | 9.89495e-05 | 0.00703313 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024307 | AACCAGAAGCTGTGG[-/GAGGT]GTATTCCGGGTAAGG | 26259 |
rs554297194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017893 | GACCCCCCAATTACA[C/G]AGTCTCAGTGCTTGC | 26259 |
rs554297511 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926940 | AAAACATTGAGGTGA[-/T]TTTTTTTTTTGTTTT | 26259 |
rs554321123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116916196 | TCTTCTGAAAAATGT[A/G]TCCACATTTTTCCTG | 26259 |
rs554382078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923075 | GCTAGATGTGGTGAT[A/G]TGTGCCTGTAATCTC | 26259 |
rs554402321 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980444 | ATGACAAGCATTAAG[C/T]AAACCTTTATTGATG | 26259 |
rs554422492 | snp | A/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987249 | CGTGTTCTGGAGGCC[A/G]GCTTTGAACTCTTTG | 26259 |
rs554433646 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956287 | GAAGGAGAACTGTAT[C/T]ATTTGCTGCAAACCA | 26259 |
rs554455968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916810 | GCAGCTTGGGCTGGG[C/T]ATGGGTGAGCTCACT | 26259 |
rs554548294 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979482 | TGAGCCCAGGGAGCA[A/G]GTGGGAGTGCCAGGC | 26259 |
rs554552778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969228 | TTGAAATCTTTGATT[C/T]GTTTCAAGTTCATTT | 26259 |
rs554553857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970774 | AAGCATTGCTTGCGA[C/G]AAGGCTAAGGCAATT | 26259 |
rs554573728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009199 | CAACATAGTGAGACC[A/G]CTTCTCTACTTAAAA | 26259 |
rs554581073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935033 | TTTTGTTTTCAGTTT[C/T]TTAATGTATATTTTA | 26259 |
rs554680196 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972607 | AGTGGCCTGGGAGCT[G/T]GGCGGCATACAGGGA | 26259 |
rs554688432 | snp | C/T | | | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032907 | GCGCTTCCCACCACA[C/T]GTGTTAGATGGCAGA | 26259 |
rs554696044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012375 | ATCCAAATTGGCATT[C/T]AACCAGTGTGAGTCC | 26259 |
rs554715819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008584 | TAGTGTTGTTTTGAC[C/T]ATTAGAAACTTCCAA | 26259 |
rs554721709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993815 | GTAAATTATTTGCCT[A/G]GGCCAATGTCCAGAA | 26259 |
rs554725876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001270 | CCTGCTGCCCTCCAC[A/C]AAAGGCCCTGATTAT | 26259 |
rs554741600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971914 | TTTAGGAATCTACAA[A/G]CCCTCAAAGTTAAGA | 26259 |
rs554753697 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030567 | ATTTTGCAGGCGCAT[C/T]CGCCCTTCCTAGTTT | 26259 |
rs554815258 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965419 | GTACGAATAGTCTAA[A/T]GTTAGCTTTATCTAT | 26259 |
rs554864672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994449 | AAAGATAGGAAGGAA[A/G]GGTATGTGGTGGGAG | 26259 |
rs554879972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956260 | ATGCTTCTCTTCTGC[C/T]TAGTGTGGTTGGAAG | 26259 |
rs554906774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007552 | CTTAAAAGGAACCAT[C/T]CTCAACATCATCTTT | 26259 |
rs554943468 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027508 | TACTCACAGGAGGTT[A/G]GTGGTGGGGCCGGGC | 26259 |
rs554946496 | snp | C/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983444 | TTTAGCTTGAAGAAG[C/G]CTCTGCTTTTGTTTA | 26259 |
rs554951082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966136 | TAGTAGACACTACTG[A/G]TGGATTTCCTTTTCA | 26259 |
rs555039290 | in-del | -/ATA | 0.0322114 | 0.122752 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028748 | TATAATTATATACTT[-/ATA]ATACAGTTTAGTCAT | 26259 |
rs555040459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921071 | TCCTGGGATTTCCCC[C/T]AGCACTTGCATTTCT | 26259 |
rs555090784 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994103 | GGCATCCCATTACCT[A/G]ACTTCAAATTATACT | 26259 |
rs555122766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998539 | CATCCTATACCATGG[A/G]AGAGAATGAACTTAG | 26259 |
rs555209043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959949 | AGTGTTCTTACATCA[C/G]CTAGTATATTAGTTG | 26259 |
rs555216212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948339 | CTCCCAGATCCTTGC[C/T]TTCCCTCCCCATATC | 26259 |
rs555239691 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116916169 | ATAGTGCCACCATAA[A/G]TGTTTTGTACATCTT | 26259 |
rs555248947 | snp | A/G | 0.000693985 | 0.0186148 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027468 | ACCAGACGGTAATGC[A/G]AAACGCCGACCTGGA | 26259 |
rs555254124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921980 | CTACAGGTGCATGCC[A/G]CCACACCTGGCTCAT | 26259 |
rs555307357 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933562 | TTGTCCACCAGAATT[A/C]TTCCCTCTATGGCCA | 26259 |
rs555372515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931028 | ACCCAGGCTAGTCTC[A/G]AACTCCTGGCTTCAA | 26259 |
rs555379466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924739 | GCTTTTGTCCAGGAT[A/G]TGGCTTCATATCCTT | 26259 |
rs555444984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917759 | GCACTTTGGGAGGCC[A/G]AGGTGGATGGATCAC | 26259 |
rs555491164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946487 | AGGCTGTTGAGCAGT[A/G]TCTCTGGCCTCTCCC | 26259 |
rs555492762 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951072 | GGGCAGGCCCCCTAC[A/G]AGTCCAGATGCCAGT | 26259 |
rs555531476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116989337 | ACTGGTAGGTGTTTA[G/T]CTTGCTTTCACTGTG | 26259 |
rs555550428 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953156 | CCCCTGCCACCTATA[C/T]ATGATGTTATATGGG | 26259 |
rs555565918 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937177 | AGTTCACTGTTTACC[A/G]ACAAGTAGCAGACCA | 26259 |
rs555578506 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032131 | TATGGTTATGGGAGG[C/G]AATTTTTATTTTACA | 26259 |
rs555579287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004542 | TATTAGGCTTGGATT[A/C]TTTTAGCCTTGCAGG | 26259 |
rs555602799 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967257 | AATGCCTGTGTAGTA[A/C]TGCATTATGTGGCTG | 26259 |
rs555630550 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939105 | AGAGCACTGGGCTTT[A/T]GAGATACTCGTTGCA | 26259 |
rs555649973 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930484 | TGCTCATTTTTAAAT[G/T]GGGTTTTTTGTCTTC | 26259 |
rs555770352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017184 | GTTTTAGTATTTCCA[A/G]CTTGGGACCATGTGC | 26259 |
rs555777430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996179 | CAGATTGTATTAAGC[A/G]GCACACGGCGTGCAT | 26259 |
rs555830028 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941208 | GGATTGCCTGGGCCC[C/G]ATTGGCCAGGGATGC | 26259 |
rs555836373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933414 | TCCAAAGAGTTTATC[A/G]GAGAAAGATAGAATC | 26259 |
rs555838723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002510 | CGGTTGCTGCTGCGA[A/C]GTGCACCTGAAAGGC | 26259 |
rs555912479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996786 | TGTGAGGGTTGCCGT[C/T]ATTGTTAATGAATGC | 26259 |
rs555941305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977518 | ATGCACCCCCGTGTA[C/T]CCATCACTCAGCTTC | 26259 |
rs555958140 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929517 | TGGGATTACAGGCAT[G/T]AGCCACTGGGCCTGG | 26259 |
rs556041521 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936421 | TAAAACGCCCTTTGC[C/T]GATGTGATTAGGTTA | 26259 |
rs556119001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927042 | AAGTCACTGATGTCA[A/G]CCAAAGCTTATTAAA | 26259 |
rs556134835 | in-del | -/TTC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116999998 | TTTTTTTTTTTTTTT[-/TTC]TTTGAGACGGAGTCT | 26259 |
rs556224214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017988 | GAGAGTGATTGGGGC[A/G]TAAATGTTGCATTTG | 26259 |
rs556250135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925639 | TAATTCTGAGAGCAC[A/G]GTGACTTTTTTTTAA | 26259 |
rs556252402 | snp | A/C | | | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964757 | CTACGTAGCCCCCTT[A/C]CTGGAATCAGAGGAC | 26259 |
rs556273658 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116993767 | AGGTGTCATTTATTT[A/G]TTTTTGTTACATTTG | 26259 |
rs556274379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976128 | AAAATCAAAAAAGAC[C/T]ATCAAATTACAGGAT | 26259 |
rs556295070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024064 | GTGTTGTGCATAGAC[C/G]AGCACCGTGGAGGGG | 26259 |
rs556303877 | snp | C/G | 0.326741 | 0.23793 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012196 | ACGCACTGCCAGGGA[C/G]GTGTTCCATGCATAG | 26259 |
rs556311552 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932022 | TACATTTCTTCTATA[C/G]CTCATTTATTAAGAG | 26259 |
rs556312327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993571 | ATGTCATTTGCCCAC[A/T]TTTTAATGGGATTAT | 26259 |
rs556312819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978319 | GTCCAACTTTATGCT[A/G]GTTTTATGTCTCTGG | 26259 |
rs556333253 | in-del | -/CAAA | 0.0364866 | 0.130046 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909647 | ACAAAACAAACCAAA[-/CAAA]CAAACAAACAAACAA | 26259 |
rs556336946 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991862 | ATTCCAGAGGTGTAA[-/T]TTTTTGTTTAGTTGG | 26259 |
rs556426850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921691 | AATGTGTTGCTTTTC[C/T]GTGTCTGTGAAAATA | 26259 |
rs556445423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005477 | GTTACAACGTGTAGT[G/T]TGATGCGGTGTGGTG | 26259 |
rs556454559 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912861 | TTAATAGCTACTATT[A/T]GAGTTTTTACCAAGT | 26259 |
rs556511147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984376 | GCCAGTGTGTGAAAG[A/G]GGAATTAATCTGGGT | 26259 |
rs556524177 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956793 | GCTAACATGGTGAAA[A/C]CCTGTCTCTACTAAA | 26259 |
rs556533642 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028468 | AGGGATCTCGCTGCG[C/T]GGTCCTATACGGTCC | 26259 |
rs556557387 | in-del | -/C | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024416 | GCTAAATGCCCCCTA[-/C]CCCCCCGGCTTCGCC | 26259 |
rs556563967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947228 | AATGAACAGGAAGTC[A/C]TGTGTTAGGTAAGTA | 26259 |
rs556565103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932689 | TACAGGTGCGCCACC[A/G]TGCCCAGCTAATTTT | 26259 |
rs556623781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926069 | AGTAGGCAAAAGACA[A/G]AAGGCTCCTGTTACT | 26259 |
rs556643916 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116976713 | TCAAGTGATCTGCCC[C/T]CCCTCAGCCTCCCAG | 26259 |
rs556649787 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014981 | TCTACCTGCCGGCAT[C/T]GCCGCCACCATGCAG | 26259 |
rs556658761 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969371 | CAACTTCTATTCTTT[C/G]CCCAGACGTCAGGTG | 26259 |
rs556700980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009914 | TGACGTAAATTCAGA[A/T]GAGAACTCATGCTGG | 26259 |
rs556720642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027095 | GCATGTGGCTGATTC[A/G]TCTGCAGTAGGGTGT | 26259 |
rs556722066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968676 | TTATGCTCTTACCAG[C/G]AAGCCATGAGAGTGT | 26259 |
rs556759291 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011029 | CCCCGGGCGCCCCAG[C/G]AACCATCAGCACAAA | 26259 |
rs556786626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009219 | TCTACTTAAAAAATT[C/T]TTTAAAAAAGAAAGA | 26259 |
rs556788272 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923621 | CTCTGCCTGCCGGGT[C/T]CACGCCATTCTCCTG | 26259 |
rs556817859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006044 | TAAAATGCTATTGTC[G/T]TGTAAGGAAGCCTTC | 26259 |
rs556861969 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999613 | CTGTCAGTGCCCCTC[C/T]TCACGGTCCACTTCA | 26259 |
rs556872998 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946068 | ACAGTGAAGTGTTTC[C/T]ATAGGAGATAACTGT | 26259 |
rs556887319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923230 | GGAGGTGCTTGAGCC[C/T]TAACCCTGGAAATTC | 26259 |
rs556933871 | snp | A/G | | | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024256 | ATCGTCAGTGGAGGC[A/G]AGGAAGGCCTGGTGT | 26259 |
rs556934714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962255 | TGCTGTTATCTGTGG[A/G]GTTCCTGCCCTCACT | 26259 |
rs556938052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964383 | TGATCCCTGTAGTGG[G/T]AGAGCTTGCAGGAGC | 26259 |
rs556946039 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955698 | GAAGAAAGGGGCATA[A/T]GGAAACATCCCTGTT | 26259 |
rs556956542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021061 | ACTCCCCAGAGAAGG[A/G]TTTCTGCTCGCCTCA | 26259 |
rs556977992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003013 | AATTCTACCATGAAG[A/G]TGTATAGGACTTTTT | 26259 |
rs556996023 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969465 | CGTGAATAGCTACTT[C/T]TGGGCAAAGACAGAT | 26259 |
rs557014521 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922675 | CATAGGAATACAAAT[C/T]AGCCTCCCTGGGGAT | 26259 |
rs557026530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116916320 | TTTCTCACTTTTGAT[A/G]GTAACTTGTGTATGT | 26259 |
rs557079228 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961118 | CTTCTGCCTCAGCCT[-/C]CCAAGTAGGTGGGAT | 26259 |
rs557080937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956397 | ATACAAAACAAAACT[G/T]CCCATACCTCTCTAG | 26259 |
rs557102436 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006762 | TGCATGTCACCCAGC[A/G]TCCCTGCACGTTCAT | 26259 |
rs557122284 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965619 | AGAATGTTAAGTGTT[A/C]ATGTCATGGCACCAC | 26259 |
rs557157378 | in-del | -/AAAC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019906 | TGTTTGGTTTTATTT[-/AAAC]AAACAGGAAGTACGC | 26259 |
rs557171072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994487 | TCCCACTCCCTCCAA[C/T]CTGCCACCCAGTTTC | 26259 |
rs557202123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958168 | GTCTTAAGCCCCACT[C/T]GATGTTTGTTGTAGT | 26259 |
rs557203208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943935 | CTCAGATAAAGACAA[A/G]CCTTGAGAATAGAGC | 26259 |
rs557225822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970771 | TTAAAGCATTGCTTG[C/T]GAGAAGGCTAAGGCA | 26259 |
rs557233243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942871 | CAACCTCTGCCTCCC[A/G]GGTTCAAATGATTTT | 26259 |
rs557245719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996337 | TTATTCCCCATACAC[A/G]GACGTGAAGAGACTC | 26259 |
rs557296648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950196 | TGTTTTTTTTTTTCT[C/G]CATGGCCAACACATT | 26259 |
rs557340305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960768 | TGATGGAGGCTATGG[C/T]ACTGCGGTAGGGCCT | 26259 |
rs557373707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914952 | ATAATTCATTGTGTG[C/T]GTAAACTGTCTCCTT | 26259 |
rs557411603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949458 | ACAGCTTAGCATGTT[A/C]GTCATCATCTTTGTC | 26259 |
rs557418068 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013610 | ATTTATTCTAAGATG[A/T]ATATTAAAAAAAAAT | 26259 |
rs557427586 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939377 | CCCTTCTTAGAGATG[C/T]GCAGCACATGCCACT | 26259 |
rs557442519 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914484 | AGGCTGATGTGGGAG[A/G]ATTGATTGAGGCCAG | 26259 |
rs557490914 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116967853 | CTCACTACAACCTCC[A/G]TCTCCTGGGGTCAGG | 26259 |
rs557549649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946586 | TGGATGTCCCCTGGG[A/G]ATCAAAATCCCCTCC | 26259 |
rs557550544 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935123 | TGTTTATCAAGTAAA[A/T]GATAGAAAAACGTGC | 26259 |
rs557556185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942219 | TTTTTTGTAGAGATG[A/G]GGTCTCACTGTTCAT | 26259 |
rs557588678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980517 | AGAGAGGGAAAAGGA[C/T]ACAGTCTTGCCATTT | 26259 |
rs557608709 | in-del | -/C | 0.0146672 | 0.084371 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953793 | AAAAAGACAAAAAAA[-/C]AAAACAAAACAAACA | 26259 |
rs557650640 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933663 | CTTAAACAGAACCCC[A/G]TTAGCGTACAGTGAC | 26259 |
rs557663644 | snp | C/T | 0.00597604 | 0.0543351 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984500 | AAGCACTGCTGCTAA[C/T]AGAGGCTTTAGGAGG | 26259 |
rs557688448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939052 | TCTTAACTGATTGAC[C/T]GGTAACCCAAATCAG | 26259 |
rs557692293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937329 | ATTTAAGGCCAGGAG[A/G]CAAATGAGAACATTA | 26259 |
rs557693953 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032799 | CAAGAGAGGGCTTGG[C/T]CCTTTCTGAAAGGAA | 26259 |
rs557695927 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913363 | TGACCTCCTTGCAGT[A/C]AAAAATCTGTGTATA | 26259 |
rs557769265 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, synonymous-codon, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116911296 | CGCTCACGTTCTCCT[C/T]TGGCCCGCGAGGGCG | 26259 |
rs557778498 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919486 | CTGAGCCTGGAGTAC[A/C]GTAAGGGCCCAATAA | 26259 |
rs557784483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004042 | TCAGGGGAGGTGTGC[A/G]TGAAGGCAGCTTCTC | 26259 |
rs557794796 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999422 | CCATCTGGCCCGGGT[C/G]GCTTCTTTGCACTCT | 26259 |
rs557833793 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116942560 | TTTATATTTTTAGTC[A/G]AGATGGGGTTTCACC | 26259 |
rs557868866 | in-del | -/T | 0.178785 | 0.239642 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940255 | ACCATCCTGGTTATC[-/T]TTTTTTTTTTTTTAA | 26259 |
rs557891357 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944801 | TTTTCTAGATCTAAT[C/G]TTACAGTCCTGGATA | 26259 |
rs557907013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997026 | ATAAATAAATGAGGA[A/G]TGAACATTCAAATGC | 26259 |
rs557946884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932090 | TTTTTCTGCACCTGA[C/G]GTGATCACATCGTTT | 26259 |
rs557951388 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028569 | CCCTTACCTCTTTTC[C/T]TCCGAGGGCCTTTGG | 26259 |
rs557952598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947003 | TGAATTCGAAGATGT[C/G]AGACCGTGGTAGAGA | 26259 |
rs558019083 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920342 | GTTTCATTCATATCC[C/T]ACAAATATTTATTAA | 26259 |
rs558042493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016316 | TTTCTCCACCTCCTC[A/C]CCAACACTTGCTACA | 26259 |
rs558049004 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927759 | GCTGCTTTGTGAAGC[A/G]CCATGGGAAATGGTC | 26259 |
rs558060187 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029122 | GGATCCAGTAGATGC[A/G]TATGGAATTTCAAAT | 26259 |
rs558070665 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994285 | TGTAAAAGTAGATAC[A/G]CAGACCAATGGAATA | 26259 |
rs558084360 | snp | C/T | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932767 | TCCATCTCTTGACCT[C/T]GTGATCCACCTGCCT | 26259 |
rs558099238 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030452 | AGAAGGTTTTCATCA[A/G]GCCCCGCCCTTTCTC | 26259 |
rs558133884 | snp | A/G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029891 | GCTGGGATTACAGGT[A/G/T]TAAGTCACTGTACCC | 26259 |
rs558177316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, splice-donor-variant, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116918727 | TTCCTGAAGATGAAG[C/G]TGAGGTCAGCTCTGC | 26259 |
rs558182839 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913879 | TCTTCCTGGAATTCA[-/T]TTCCCTGGTCTCCTC | 26259 |
rs558188007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116974506 | TGGAAAGCAAGCCAC[A/G]AAAGGATCCAGCCGA | 26259 |
rs558197821 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968003 | GAACTCCTGACCTCA[A/C]GTGATCTGCCTGTCT | 26259 |
rs558209473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026021 | CACAAGGCTGACAGA[C/T]ACATGGTCTCCTGCC | 26259 |
rs558210576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022851 | CTCCTTTACAGATGT[A/G]TTTTTCATGCATAGC | 26259 |
rs558228156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927618 | GGGAAGAGGGGTGGC[C/T]TCCCTGATTTCAAGC | 26259 |
rs558231080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937923 | GACACTTTTATTAGC[A/C]AGTCCTTGCAGCTGA | 26259 |
rs558239971 | in-del | -/ATCT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022971 | GGTCCCACTTAAGCC[-/ATCT]ATCTGTCTTCTTGTT | 26259 |
rs558265497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994406 | GTATTTTTTGACTGG[G/T]TAATGCATTCACCTA | 26259 |
rs558305569 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922481 | CAGAGAGATCTTTCA[C/T]GTCCTCTTTGCCCTG | 26259 |
rs558362585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924118 | TCCTTTTCCTTCTTC[G/T]TGGAATATCTTTGTT | 26259 |
rs558366896 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928331 | GTATCTTTCTGTGAC[C/G]CAAGAGCTCTTTTCT | 26259 |
rs558412376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956536 | GTTTGCAGTTCTTTG[C/T]AGACAGAGAGCAAAA | 26259 |
rs558422041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020882 | TTTTTAAGCGTTTTA[C/T]AGTGGAACTGTCAAC | 26259 |
rs558441456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017014 | GTTCTGGCACTACCA[C/T]GCTGTACAGCTTTTT | 26259 |
rs558475582 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030279 | GCGCTTTCTTTCAGA[A/C]CCTGCCTACCTGCAG | 26259 |
rs558486581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934129 | ATTATCCCACAAACC[A/G]TGCCGGAGACTGATT | 26259 |
rs558498312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010732 | GGGAGACCACTTGGA[A/G]TATCTTTTGTCCCCT | 26259 |
rs558499656 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011739 | GAGCTCTTTGGGATG[C/G]TGGATGGTGCTCAGA | 26259 |
rs558519571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977336 | CACTAGAATTTTCAC[C/T]GTAGATCTGAGAAGA | 26259 |
rs558544879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941313 | AACCACTGGAGACTG[A/G]GACAGCGTGACACTC | 26259 |
rs558699793 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026131 | CATGTACCTCCCGCT[C/G]TCCGCTTCAGTCTCT | 26259 |
rs558711396 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006659 | CTCAGAGAGGCAGGC[C/T]CCGTCTATGGAGGAG | 26259 |
rs558718287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986496 | AGCCGGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC | 26259 |
rs558722985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971802 | ACCAGAATTTACACT[C/T]TGTGTTTGAGGCTGT | 26259 |
rs558774637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006289 | TCACAGTGATTTCAG[C/T]ATGCAAGTGGTTCAT | 26259 |
rs558774649 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012959 | TTATTTTGGGGGTGT[G/T]GGGGGACAGTGAGCT | 26259 |
rs558796101 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913440 | CAGAAGCCTTATAGA[G/T]AAGTCAGTTAACACA | 26259 |
rs558823891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915023 | TCTCCCAACAACTCT[C/T]TCCAGTGGCTATTTT | 26259 |
rs558857128 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917347 | TGCTTGATCCATGGG[C/T]GGCTCCTGAAAGGAA | 26259 |
rs558857501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964471 | TATTGTTTTCTCATT[A/T]GAAATTGTCACCATT | 26259 |
rs558890633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963084 | GTCAACCCAGAGGTA[C/T]AGCAGGCCAGGTTCA | 26259 |
rs558893221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009319 | ATTGGCTGAGCCCAG[A/G]AGTTTGAGGCTACAG | 26259 |
rs558954991 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008845 | CTGGCTCATGCCTGT[A/G]ATCTCAGCATTTTGG | 26259 |
rs558978593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962359 | GCTAAAGTACCTTTT[C/T]CCCAAGCTTTGTTGT | 26259 |
rs558987788 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025481 | TGAGAACACAACCTC[G/T]GAGCAGCGACATGGT | 26259 |
rs559018622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920951 | CTGTCTTCTCTCCTC[A/G]CCATGTCCTAAAGCT | 26259 |
rs559031737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002618 | GTGTTACCAAGCCTC[A/C]CGCTATGACTTATCT | 26259 |
rs559050214 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022867 | TTTTTCATGCATAGC[A/T]TATATTTTTACTTTG | 26259 |
rs559069589 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116949560 | GAAAAAGCACGATGC[G/T]TGGCTTTCGGGCTGT | 26259 |
rs559121492 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116916462 | TACATGCCATGGCTG[C/G]GGTCAGGGTAATAAC | 26259 |
rs559134714 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002201 | GTCCAGTCCTGGAAC[A/G]GCGGGGGTTGCAGGT | 26259 |
rs559152849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913094 | ACTTGAGGCTTGGTT[A/G]TAATATAGGTTCTGG | 26259 |
rs559154260 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000472 | CATCAGAATCTACAG[C/G/T]AGACCTGATGAAAAC | 26259 |
rs559166654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993664 | TTTGTTGGATATATA[C/G]TTTGCAAATATTTTC | 26259 |
rs559202351 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955040 | CCCTCTTGAAATGGG[C/G]GGGGGGGGCCCTGTA | 26259 |
rs559216492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027577 | CCCACCCCCCCCGCC[A/G]TGACACATTGCACCC | 26259 |
rs559218453 | snp | A/T | 0.115438 | 0.210697 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022356 | ACTAAAGAAACTATT[A/T]AAAAAAAAAAAAAAC | 26259 |
rs559250277 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116923354 | TGGTAGAGAATCGAT[A/G]TCTGAGACATTGTCA | 26259 |
rs559257155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027314 | CTAGAATCCCCTGCA[A/G]CTCTGAACTCCCAGG | 26259 |
rs559268772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988601 | ATGTGTAGGTGGAAT[C/T]GCATATTTTTGATCA | 26259 |
rs559276010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948210 | TGTTTTTTTTCCTAG[C/T]GTTTGCATAAATGCA | 26259 |
rs559300855 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948513 | TGGAATGATGTCATC[-/T]TTTTCCTAATAATAG | 26259 |
rs559329829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996403 | ATCTGTCTGGGAGAG[C/T]CTTAGGAATCAGAAA | 26259 |
rs559337031 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947682 | AGGTGGAGGTTGCAG[G/T]GAGCCAAGATTGCGC | 26259 |
rs559339878 | snp | A/G/T | 6.59308e-05 | 0.00574123 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949583 | CGGGCTGTCCCGAGA[A/G/T]CAGTCTAAACTGCAT | 26259 |
rs559357473 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031433 | ATGAAACTAATTTTG[C/G]CTGGGCAAGGTGGCT | 26259 |
rs559416426 | snp | G/T | 0.00214291 | 0.0326629 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964817 | TGTCTCCTTTGTGAG[G/T]ATAAACAGCTCGTTG | 26259 |
rs559440728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958246 | TAATTGCATAATACA[A/G]CCCCATCGTGTTTCA | 26259 |
rs559441911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942244 | GTTCATCAGTGTGGC[C/T]TCAACTCATTGAGCA | 26259 |
rs559471764 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943565 | TGCTCTCTGTATATT[C/G]GGGTACTGCTTCACC | 26259 |
rs559532061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950789 | ACTTGCGATTCTGTC[C/T]ATTAAGTTATCGATG | 26259 |
rs559583881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935249 | ATAAATAAGTAATTC[C/T]AGAACCAAAGACCAG | 26259 |
rs559608831 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921031 | TTTTGCTTCACACCA[C/T]CCTCCTTCACCACCA | 26259 |
rs559622765 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989667 | ATTTATAGAACTCTC[C/T]CTACCAGTGGGACCA | 26259 |
rs559648351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973989 | CTAGACATTGGAAAA[C/T]AAGTAGCCCATGGCT | 26259 |
rs559649056 | snp | A/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975209 | AAGAATCACCAGCGG[A/T]TGTTAAAATCAATGT | 26259 |
rs559652971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972824 | GTCGTATGTATATAT[A/G]TTTATGTGTGTCCTG | 26259 |
rs559659732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021165 | CCTTTGCTGGGTAGA[C/T]TGGTGACAAGTGGCA | 26259 |
rs559672969 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937675 | TGGCTCAGGAGCAAG[A/T]GGAGAGAGAGGAAAC | 26259 |
rs559706854 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981666 | TCACCCAGGCTGGAG[G/T]GCAGTGGCACTATCT | 26259 |
rs559712747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941663 | TTGACACCAAGATAA[A/T]CTGAGTTCTTAGATT | 26259 |
rs559734208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946606 | AAATCCCCTCCCAGT[C/T]GAGAACCACTGTTCT | 26259 |
rs559789688 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014644 | TCAGACGGCAAGTTC[G/T]GTTTACCCTTTGTGG | 26259 |
rs559854926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014147 | TTTCTGTTCTTCAGG[C/T]TGCATCATCTCCGTT | 26259 |
rs559870981 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983336 | CCAAAATAATTGCCA[C/G]GGGAATGTGCTGTGG | 26259 |
rs559904021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020532 | GCAGTTTTCATATTT[A/C]TCTCTTTGTGCTCCA | 26259 |
rs559915120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968931 | GGATTAGCATGCAGT[A/G]TGGTTCCAAGTACAT | 26259 |
rs559917942 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025684 | CTGTTGAGGGCGCCT[C/G]GGCCCTTTTTCTGAA | 26259 |
rs559919915 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030601 | GCAATTAAAGATAAC[A/G]GAGTGTAAAGTCATT | 26259 |
rs559976865 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954914 | CTCCATCCCAGCCCC[A/G]CTGTGCTGCACTCTC | 26259 |
rs559993617 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026774 | AGGCATCCACCTGGA[C/G/T]GAGACATCTTTTTAA | 26259 |
rs560038891 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984620 | TGCTACATGTAGGAA[A/G]TTTCACATCTAACTT | 26259 |
rs560043193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011449 | TATGCTTTATTGGGA[A/G]GAAAAATAAGGCCTC | 26259 |
rs560049926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939166 | AAATGCAGCTTCTTA[C/T]ACAGGTTGAACTTCC | 26259 |
rs560078165 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991273 | TACCAAGCTTCATCT[A/G]TGTAACTTTGCTTAT | 26259 |
rs560086637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923320 | TTAATGTGTAATACA[A/G]GACGAAAGTCCCCAA | 26259 |
rs560098376 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017559 | AGCTATTGATTTTGG[C/T]ATATAAGGTTATATT | 26259 |
rs560121449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022979 | CTTAAGCCATCTGTC[G/T]TCTTGTTCTGGTATT | 26259 |
rs560181937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932214 | CCTTTGATGGACAAC[C/T]GTATTCTCTAGGAGA | 26259 |
rs560190003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912003 | GGGGACCCTGTGTCC[A/G]TTAAAAATAATCCCC | 26259 |
rs560213010 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961170 | CTGGCTAATTTTTGC[A/G]TTTTTAGTAGAGACG | 26259 |
rs560213970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027967 | CTGCACAGACAGAAG[C/T]GGCTGGGGTGAGGGC | 26259 |
rs560216334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983952 | AGCTCCCCTAAGTCC[A/G]TCAGCTAACAAGTGC | 26259 |
rs560316264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952267 | GTGTAAGAACACTCT[A/G]TGATGTTTGCACAAA | 26259 |
rs560325776 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012600 | TACATTTTTTCCCCG[A/G]AGGTTTAATAGCTAT | 26259 |
rs560360052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018200 | TGTGATTTTCATTAG[A/G]GAGGGGCTGGAGAGA | 26259 |
rs560398620 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024420 | AAATGCCCCCTACCC[A/C]CCGGCTTCGCCAGGT | 26259 |
rs560450815 | in-del | -/TGTT | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020441 | TAGCTGTCCGCACTC[-/TGTT]TTTCTCCTTCCGGAA | 26259 |
rs560451677 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952762 | TATTGTTTTGAGACA[C/T]AGTCTCACTCTGTCG | 26259 |
rs560480701 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925441 | AGAATTACTCTAAGT[A/G]TGCGGCATGAAACTT | 26259 |
rs560489630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116974681 | GCCTGGGAGGTCAAG[C/G]CTCCAGTGAGCCATG | 26259 |
rs560517924 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029679 | CAATGGCCTGATCTC[A/G]GCTCACTGCAACCTC | 26259 |
rs560562162 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930796 | TTTAAGATTTTAATC[A/C]GTTTTGAACTTATTT | 26259 |
rs560578637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921243 | TGCACTGAGCTGGTT[A/G]GATTCTATAGTATTA | 26259 |
rs560606526 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968131 | GTGTGAACAATGTTA[A/T]TTTTTTAATCTAAAA | 26259 |
rs560635918 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004127 | CATTCCGCCCAATTC[C/G]TCAACTCGGTATTCC | 26259 |
rs560657950 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027743 | GAGAGGGAGGGCAAG[C/T]CGTATGCTGAGGGGC | 26259 |
rs560689548 | in-del | -/GTGC | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978271 | AATCTCCCACCGGCA[-/GTGC]CCTCTTCCATGAAGA | 26259 |
rs560712422 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910594 | TCCTAATACCTATCA[C/T]TGATTTAAATGTTCA | 26259 |
rs560732035 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028852 | AAACAGCCATCAAGA[-/T]TGAAACAGGACAGGA | 26259 |
rs560760377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948794 | GGTTCTCACTCTCTT[G/T]CCCAGGCTGAAGTAC | 26259 |
rs560767345 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010843 | AAATAGGGTTTCCTG[C/T]CAAACGATGTCAAGA | 26259 |
rs560770523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998133 | CCCCAAGAATTGTTT[C/T]AAAAGAATGCATTTA | 26259 |
rs560787433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915055 | AACTAATCTGTAGAT[A/G]AGCATTAGGAAAGTA | 26259 |
rs560813699 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021436 | TAGGAAAAAGTTAAA[-/C]CCTTTTTTCACCTTC | 26259 |
rs560826858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942351 | GAGTAGATAATCTCA[A/G]TTGACTTGCTTTAAG | 26259 |
rs560856558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971177 | AGACCAGCCTGGGCA[A/G]CATAGTGAGCCTCCG | 26259 |
rs560925266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956595 | AATTGGTGTCTGAAT[C/T]TTTGGTTGGTTCAGT | 26259 |
rs560940456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964583 | AGTGCCTCAGCAGTG[A/G]CTCTACACCACCCGA | 26259 |
rs560954366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007765 | ATAATTAATCTCACT[A/G]GTCTATGGCAATCAG | 26259 |
rs560991463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963712 | CAGTGAATCTCAGAG[G/T]TTATCTCATCAACTC | 26259 |
rs561050455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000157 | TGCCTTTTGTATTTT[C/T]AGTAGAGACGTGGTT | 26259 |
rs561089155 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927270 | TCTCAAATAAAGCCC[A/G]TTACCTCATCTCTAA | 26259 |
rs561092632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000995 | CTTAAAATTATTTAA[A/G]CCTCAGTTTCTTGAT | 26259 |
rs561095604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006313 | GGTTCATGATTAATT[A/G]TGAGGGTGATAGCCC | 26259 |
rs561188262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993216 | TCAAGCAGTTCTCCA[A/G]CCTTAGCCTCCCGAG | 26259 |
rs561220082 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947009 | CGAAGATGTCAGACC[A/G]TGGTAGAGAAAAGCA | 26259 |
rs561230717 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992400 | TATGTATTTTTGCCC[C/T]TTTTTTTTTGAAGAT | 26259 |
rs561236565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975363 | AGATTCTATGTCTGG[C/T]GAGAGCCCTTCCTTC | 26259 |
rs561280807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025214 | CATTCGGCCAGACAC[A/G]TGGCTCACCTGTAAT | 26259 |
rs561283422 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944535 | TTGGATGGATGGCAA[A/G]CATCAGGCACTTGAT | 26259 |
rs561283467 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116974672 | ATCACTTGAGCCTGG[A/G]AGGTCAAGGCTCCAG | 26259 |
rs561311147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996450 | TGTGGCCACATTCTC[C/G]CATACCTCCACCCGA | 26259 |
rs561351737 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925290 | TGTTTGGCCAAAGGC[A/G]TTGCCTAGGAAGGGA | 26259 |
rs561373403 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912653 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT | 26259 |
rs561374456 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978641 | GTGGAAGCTCAAGAG[G/T]ATGGGAGCTCGCGGC | 26259 |
rs561452724 | snp | A/G | 1.65307e-05 | 0.0028749 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988865 | GGGTGTACGAAGGAA[A/G]CAAGGTACACAACTA | 26259 |
rs561479555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940640 | AGCAATCTTTTCTTT[C/T]GTCTGCAGGGTGGCG | 26259 |
rs561482754 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116993648 | TTCTGGATATTAGTC[C/T]TTTGTTGGATATATA | 26259 |
rs561509304 | snp | C/T | 0.000199843 | 0.00999409 | missense, intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985395 | CGGAATTTGAAGTTC[C/T]GAAACTGGTGAGCTT | 26259 |
rs561541595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951454 | TGTATCTCCAAGGAG[C/T]TTCTTAAAGAGACAG | 26259 |
rs561547670 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998304 | TCTTTATTCACACTT[-/G]GCCTAGTTCCTGTAT | 26259 |
rs561577059 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011068 | AGTGTTTGAAAAGAC[C/T]CTTTGAGTCCAAATT | 26259 |
rs561591356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989688 | AGTGGGACCAAGGGG[A/G]AGAGAGAGAAAGTTT | 26259 |
rs561598683 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027568 | GTATAGAACCCCACC[A/C]CCCCCGCCGTGACAC | 26259 |
rs561618471 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032442 | CCCAGCCGGGAATCA[A/G]TTTTTTTCTCAATGT | 26259 |
rs561619025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927215 | CTGTTTCACACTCAT[A/T]TTTCTTTGTGCTACC | 26259 |
rs561648235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023491 | TATCTAATTTATCCT[C/T]GTGAAAAATTCCACA | 26259 |
rs561681125 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960702 | TCAGGTTGTTACCTG[C/T]GGACACCCCCTTTCA | 26259 |
rs561686419 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008407 | ACTTACTTGGAAGAA[G/T]AAATTTACTCTTGAT | 26259 |
rs561707720 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909084 | CAACTCAGAGATGCT[C/G]TTTCTTTTTTTTGTT | 26259 |
rs561713536 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982428 | AATCAACTCATCAAG[A/G]GGACATACAATCCTA | 26259 |
rs561751860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936894 | TTGGAGTGCTTTGAG[C/G]AGAGGGGTGACAAGG | 26259 |
rs561752137 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945042 | AAGCTCTGTATGATT[A/G]TATAGCTAATTACCA | 26259 |
rs561761711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943083 | ATCATTATCTTCTAT[A/G]TGGTAAGACATTGTT | 26259 |
rs561761759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935422 | GCTGAATTGATTTTC[A/C]TGGCAAAAGTGATTC | 26259 |
rs561798584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972892 | CCAGCTGTTGAAAGT[A/G]TCACTATCTACTAAA | 26259 |
rs561812838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944254 | CCGAAAAAGTTGATC[A/G]ATCATTTTTGGTGGA | 26259 |
rs561849005 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032029 | AAAAATTGTCAGGAG[C/T]GCCTCCTTCCACCAC | 26259 |
rs561916586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967754 | TTCCGATATTTTTTC[C/T]GTAAGTCACTTATTC | 26259 |
rs561928548 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018173 | TTGGTGGGCTACCGC[C/T]GACTCCTATGGTGTG | 26259 |
rs561933926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973666 | CTCTTCAGCACTGTC[A/G]AGGTCATGAAACTCA | 26259 |
rs561935783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965889 | TCAGTCTCCTGAGTA[G/T]CTGGGACTACAGGCG | 26259 |
rs561961451 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031309 | AACCTCCCCTACAGG[C/T]GCTCCCAGCCCAGGA | 26259 |
rs562029865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983130 | TCTATGCAAATGGGA[G/T]TTTTTTTTCTCTTTA | 26259 |
rs562068641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928536 | ACGAGGACAGAACAT[A/G]TTTTAGGTGAAGTCA | 26259 |
rs562077708 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026826 | GCCGTGACCACAGCC[A/G]GTACTGCATGAAAGT | 26259 |
rs562137665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026422 | CCTGCCCTCCCTTCC[A/C]GGGTCTTTCTCATCC | 26259 |
rs562149735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987160 | CCTTTGTGATGGACC[C/G]GCAGCTTGCGGAGCT | 26259 |
rs562162813 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021258 | GTTTAAAAGCCATTA[G/T]TATTTTTCTGTGAAT | 26259 |
rs562168320 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939659 | ACAAAAAAGGCATAT[A/G]TATGCCCAGGATCAG | 26259 |
rs562173358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923333 | CAGGACGAAAGTCCC[C/G]AATAGTGGTAGAGAA | 26259 |
rs562218554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958484 | CTTTAAACCACTTCC[A/G]TCTTCTGGGTTTAAG | 26259 |
rs562232217 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116916504 | TTAGCTGGTTGTTGC[A/C]CTGTAGGAATGTGGT | 26259 |
rs562239632 | in-del | -/T/TT | 0.210584 | 0.260378 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992425 | AAGATCAGAGTTTTG[-/T/TT]TTTTTTTTTTAATTC | 26259 |
rs562260685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008935 | AGCCAGGTGTGGTGG[C/T]GGGCGCCTGTAGTCC | 26259 |
rs562278593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022014 | TGCTCTCAGGGTTAG[A/G]CTTTGGTAATAGAAT | 26259 |
rs562304216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925949 | ATGCTGGGTTGCATC[A/C]CAGGGATTATGGTGG | 26259 |
rs562344927 | snp | A/T | 3.29696e-05 | 0.00406001 | missense, stop-lost, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024175 | GACCTCCGCAGTGGT[A/T]ACATCGCCCTGTCGC | 26259 |
rs562391410 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992219 | GCTGATCAGTCACCT[C/T]CAGCTCGGGTAGGAA | 26259 |
rs562458700 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929362 | GCCTCAGCCACCCGC[A/G]TAGCTGGGATTACAG | 26259 |
rs562466965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024436 | CCGGCTTCGCCAGGT[A/G]AATCCTTACTGTGAC | 26259 |
rs562470565 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962520 | CAGTGTGCAGACTGC[A/T]GGTGTGGTGTGACAC | 26259 |
rs562475180 | in-del | -/CTGCCTCTGTCCCTGTG | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025948 | GGCCCTGTCCCAGCA[-/CTGCCTCTGTCCCTGTG]CGGTCCAGGCTTGTC | 26259 |
rs562485075 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984844 | CTAAATTAAAAATTA[C/G]CTGGGTATGGTGGCA | 26259 |
rs562511667 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FBXW8 | GRCh38.p7 | 12:116918878 | AACTGAGAATACAGT[A/C]GTCCCACCTTATCCA | 26259 |
rs562518273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005892 | TCATCTTCAGGAAGT[A/G]TAGTCACATCTTCCT | 26259 |
rs562556138 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016572 | CATTCTGTGGGTTGT[C/G]TTTTCGCTTTCTACA | 26259 |
rs562600639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926500 | AAGTTGTATCTGGGC[C/T]GAGAGAGAAAGTGAT | 26259 |
rs562642484 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912677 | ACTGTGTTAGCCAGG[A/C]TGGTCTCGATCTCCT | 26259 |
rs562646884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012536 | TAAAAATTGCACATC[C/T]AGAAAAAAGGAATGA | 26259 |
rs562647903 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910664 | CCAAGACGTCAGAGT[A/T]TTTGTTTTGTTTTAC | 26259 |
rs562654013 | snp | A/G | | | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032546 | TTTCTGGGAAAAAGC[A/G]TGGTTACCTCGCATC | 26259 |
rs562786043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116911701 | AAAAAAATTATCCAG[A/G]ACAAAATATCAGTAA | 26259 |
rs562811982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006378 | TCTTACTGGGTGAAG[C/G]AAGAAGTTGGTCTGC | 26259 |
rs562829070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939244 | TTCAGTGCTCATTGG[A/G]GCATTTTGGATTTTG | 26259 |
rs562830859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004243 | CAAATCTGCTTAATC[C/T]GATTTCCTACTTTTT | 26259 |
rs562930385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925237 | GATACAGGCTGCCTT[A/C]GTGGGGTGGGAGGGG | 26259 |
rs562943251 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961003 | AAACATTGATGCCTG[G/T]TTCTATCCCCAAATG | 26259 |
rs562948045 | in-del | -/GCTCTTCCCACCCCCTT | 0.00159617 | 0.0282053 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031218 | CATGCCACGATTCCA[-/GCTCTTCCCACCCCCTT]GAAATCTTACCTCCC | 26259 |
rs562978420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914609 | GGCTGGGCCTGGTGG[C/T]TCATACCTGTAATCC | 26259 |
rs562992652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931922 | GTGTGCATCCTTGTC[C/T]TATTCCTGAAGAAAA | 26259 |
rs563006307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960332 | GGTTAGATTTGAGAG[C/G]CCGCTGCTGAGTCAT | 26259 |
rs563038880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984609 | CACTGACATGATGCT[A/G]CATGTAGGAAATTTC | 26259 |
rs563081101 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009198 | GCAACATAGTGAGAC[C/T]GCTTCTCTACTTAAA | 26259 |
rs563106780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915157 | CTTGGATTCCTGTGT[C/T]AGTGGTTGCAAGCCC | 26259 |
rs563109322 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021403 | TCATTGGACTGACTT[-/TC]TGATTGTTCCCCCCA | 26259 |
rs563151672 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964506 | TGTGAGAATGTGAAG[C/T]GTGTTCACAGCCTTC | 26259 |
rs563156620 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985075 | AACGTAAGTGATTTC[A/G]TGTTTAGACTTGGGT | 26259 |
rs563179396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991490 | AATAGTCTCATGTGC[A/G]AGGCTTGGTGTCACT | 26259 |
rs563209929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020984 | TGTAGCTACCTCCTC[A/G]AAGTGGAATTGCCGG | 26259 |
rs563223318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936183 | GAGCAAAGACCTGAA[A/G]GAGGGGTGAAGGACA | 26259 |
rs563233830 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948405 | TTTTATCTCTCAGCC[-/TT]TTAGACTCATTCCTT | 26259 |
rs563245977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946689 | CAGGTCACGCTGGCC[A/C]CACAGTGCCCTTTTC | 26259 |
rs563264722 | snp | A/G/T | 0.000346169 | 0.0131518 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964678 | TCCTTTTGGAACCAA[A/G/T]TGTGTCGTTCTCTTC | 26259 |
rs563309262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993304 | AGACGAAGTTTCACC[A/G]TGTTGGCCAGGCTGG | 26259 |
rs563325008 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917866 | GTGTGGTGGCACGTG[C/T]CTGTAGTCCCAGCTA | 26259 |
rs563343627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957349 | ACTGTCTCAAAAAAA[A/T]TTTTTTTTTAAAAAA | 26259 |
rs563346780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950723 | TTTAGAGGTGAAAGC[C/T]CTTCTTGGGAGTGCT | 26259 |
rs563349935 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924675 | ATCAGAGTGCCTAAG[A/T]CATTCTGCTGCCCGA | 26259 |
rs563383269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002255 | GCGCACACAGGCCTT[G/T]CCTACCCAGCGCCTG | 26259 |
rs563401472 | in-del | -/GA/GTGTGTGA | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916909 | TGTGTGTGTGTGTGT[-/GA/GTGTGTGA]GTGAGAGAGAGAGAG | 26259 |
rs563405227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956703 | GCAGGCACAGTGGCT[C/G]ATGCCTGTACTCCCA | 26259 |
rs563419196 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002355 | CTTAAACATGAAAGC[A/G]GCTCAGGCTGCTTCT | 26259 |
rs563486782 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992886 | CCTGCAATAAACATA[C/T]GTGTACAGGTGTCTT | 26259 |
rs563499482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000894 | ATTGTGATATGGTCA[A/C]AAAGTGGCGCAGGAA | 26259 |
rs563504369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942484 | GGTTCAAGTGATTCT[C/G]CTGCCTCAGCCTCCC | 26259 |
rs563506269 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022480 | GCAACACAGCAAAAC[C/T]GTCTCTACTGAAAAT | 26259 |
rs563532453 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980807 | AAAGTTAAGCTTATT[A/C]ATTGTTCCATTGTGC | 26259 |
rs563534244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988549 | TGAGTGTTTCATTTG[C/G]CCATCTTTTTCTGTT | 26259 |
rs563547091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994998 | CTAGTGGTTCTTGGA[C/T]GGCTTTTCTCTGATA | 26259 |
rs563558201 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965563 | ATCTCCACAAGCTTC[A/G]TGTCCCCACTTGCCC | 26259 |
rs563617200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941484 | GCTTATCACACATGG[A/C]GCTTGTGTGCACACA | 26259 |
rs563631204 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012174 | GGAGCAAGCTGCCTC[A/G]TTATGTACGCACTGC | 26259 |
rs563679790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948546 | ATAATAATAATAATG[A/G]CTACCACTTATTGAA | 26259 |
rs563721714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989851 | ATGCCTCAGTTTCCT[C/T]ATTTGTAAAATAGAG | 26259 |
rs563728581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000326 | CTATTGCCTCCCCAG[A/G]TTGGCAGCAATTTGG | 26259 |
rs563760399 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030082 | CCTCTCAGTTGCACA[C/T]GTGTACGTATCAGTG | 26259 |
rs563797111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983257 | ATCTCCCATCTGATA[C/T]GTAGAGCCACTGGCA | 26259 |
rs563849244 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017813 | GCTTGCCATCAGCTA[C/T]GGTGTTCCTCATTAT | 26259 |
rs563863436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927811 | ATAAGGAGTGAAGGC[A/G]TGTGGGGGTCAGAGA | 26259 |
rs563871359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019949 | GGCCTCAAAAGCAGA[C/G]TAGCCTAGAGGGCGA | 26259 |
rs563896625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934321 | ACTTAATCTCTCTGT[A/G]GGAGTGTTTCTTGCC | 26259 |
rs563910267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025662 | CGCCCCCTCGCTGTG[C/G]CTGTGCCTGTTGAGG | 26259 |
rs563926684 | in-del | -/GCCACAA | 0.0252325 | 0.109451 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910841 | ACCTCTGCTTTGGGC[-/GCCACAA]GCCACAAGCCACAAG | 26259 |
rs563934153 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945218 | ATTTGCTTGTATTTT[G/T]TTTTCCACCTCATAG | 26259 |
rs563973857 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004332 | TGATCTTGCCTGGAA[A/G]TCTAATTCTCCTTGT | 26259 |
rs564003722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922083 | GATCTGTCTATCTCA[A/G]TCACCCAAAGTGTTG | 26259 |
rs564035368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010984 | CTGGCTTAGGGAGTC[A/G]GATTTTCCCGGTATA | 26259 |
rs564096425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929589 | AATGGACAAATAAAG[A/T]TATATATATGTATCA | 26259 |
rs564132107 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936957 | CTGCTGTGTGGAGAA[A/T]CGGTTGTTGGGGGAC | 26259 |
rs564156013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930903 | GCCTCAAACTTTTGG[C/G]CTCACGTGATTCTCC | 26259 |
rs564190957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938573 | TGCTTTCAGCTTCCA[A/G]CATCTTTAAGGTCCG | 26259 |
rs564200508 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032967 | CAGTTGCTGAGAAAC[A/G]GCTTCCCCTGGTGAG | 26259 |
rs564200624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027697 | GATGCAGGACAGCCC[C/T]GTGGGGCGAGTCCAC | 26259 |
rs564208261 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014877 | CCTTTCTTGAGATTC[C/G]TCCTCTCTCAATCCT | 26259 |
rs564235427 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925244 | GCTGCCTTAGTGGGG[G/T]GGGAGGGGATGCAAC | 26259 |
rs564250760 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945781 | GATTGGGTTGCCAGC[C/G]ACTTCCTCTCGGATT | 26259 |
rs564255498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968256 | TGCTGCCACCCACTT[C/T]TGTCTGCTCCATTCT | 26259 |
rs564334043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958697 | TCATACAGGCTCAGC[A/C]TCAGGCTAGCTTCCT | 26259 |
rs564371660 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925653 | CAGTGACTTTTTTTT[A/T]AAAAAAGTTTGGCTG | 26259 |
rs564375297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968784 | CCAAGTGTAGTTTTA[A/G]TTTACATTTCTCTTA | 26259 |
rs564443003 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012424 | GTGCCCACTGCTGGT[A/G]CATTAGGGGCCAGCC | 26259 |
rs564466877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923450 | ATATTTTGAATTTAT[C/T]GGTTTCCTATAGAAT | 26259 |
rs564472901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951524 | GTTTCTCTTATTCTT[C/T]TTTTTTCCTTCCCTT | 26259 |
rs564472957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959246 | TGGGTTAGGGTCAGG[G/T]GCTGTGTCCTGCAAA | 26259 |
rs564545058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025187 | GCTGCCCTCAGCACC[A/G]CTGTGAAGAGACATT | 26259 |
rs564559541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933643 | ATATAAGAATAGAAA[A/G]TATTCTTAAACAGAA | 26259 |
rs564561597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926676 | GTATGGTCAAAATTT[A/C]TCTCTTGATTTAACA | 26259 |
rs564637372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003306 | GAGCCCCTCCTATGT[A/G]CCAAACACTGCACAG | 26259 |
rs564642594 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909139 | TCGCCCAAGCTGGAG[C/T]GTAGTGGTGTGAATA | 26259 |
rs564642656 | snp | C/G | 4.94637e-05 | 0.00497287 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010316 | CACATTTCTCTTCCT[C/G]TCTCAGATCCTGGTG | 26259 |
rs564673641 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116961094 | CTCCACCTCCCAGTT[C/G]AAGCGATTCTTCTGC | 26259 |
rs564722428 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970031 | TTAGATAAAGCAGGC[A/G]AAGGTTCTGAGTAAT | 26259 |
rs564732552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018491 | AAGGCGCACGGCATT[C/T]GGGCCTGTGCTGCGC | 26259 |
rs564741500 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955172 | ACTCTCTGGACTTCC[A/G]TTACCTCCGTGAGCG | 26259 |
rs564745317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977592 | GATTCCCCACTCCCC[C/T]CCTTAGAGGCATCTG | 26259 |
rs564756460 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935694 | ACATTGAGCTAAGTG[G/T]TGGGTACTTTGGAGT | 26259 |
rs564818891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948698 | ATCTCACTTTTCCCA[A/G]CCTCCCACATGTAAA | 26259 |
rs564866363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019215 | TTTGTAGCAACGGAC[C/T]TATTATGTATCATCT | 26259 |
rs564868920 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977635 | TCTGCTGATCTCTTC[A/G]GGATAGAGTCTATAT | 26259 |
rs564876438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947934 | ACGCTCAGTGCTCAG[C/G]CGAGGTTGGCTGTAG | 26259 |
rs564878395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955822 | AAAAGACAGTATAAA[A/G]CCTGAGGTGCAGGGC | 26259 |
rs564889220 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025518 | GGAAGTGCAAGGTCA[A/G]CAATTTGACAGGTGT | 26259 |
rs564904179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914450 | TGGTGGCATGTTCCT[A/G]TAGTCCTCACTACCT | 26259 |
rs564963343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962591 | GAAATACAGTTTCCT[A/G]GTTTATGTACTTCTT | 26259 |
rs564966136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013189 | GGAGGTTGCAGTGAG[C/T]TGAGATCACACCACT | 26259 |
rs564972703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011366 | TTATTCTGTCAAATA[A/C]TATTTTCACCTCCCA | 26259 |
rs564991529 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998300 | TTTTGTCTTTATTCA[C/T]ACTTGCCTAGTTCCT | 26259 |
rs564991790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921170 | TGGAAAGCCTATTCT[C/G]GTAAAAAAAGGATAA | 26259 |
rs565025898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970450 | TGTGGCTGCCCTGGG[C/T]GGAGGTGACTATGAT | 26259 |
rs565045653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007154 | TATCATATTTGAAAT[C/G]AGAAAAAGATTTTTA | 26259 |
rs565049077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005685 | AGGGGAATGGGCACT[A/G]TGTGCCAAGGACATC | 26259 |
rs565094766 | snp | A/C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116923335 | GGACGAAAGTCCCCA[A/C/G]TAGTGGTAGAGAATC | 26259 |
rs565107886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006425 | CTCCCACCCCCACAG[C/G]GACAAGAGCCATCTC | 26259 |
rs565123619 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913329 | TTGACCTTTGAACAA[C/G]CTGGGGGGTTAGGAG | 26259 |
rs565170568 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925572 | TGGTTACCAACATGG[A/C]AGGTCATCTACATGA | 26259 |
rs565170875 | snp | C/T | 0.0126979 | 0.078662 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116910966 | CGGCCGCGGCGGACA[C/T]TTCCCTGGGCGGGAC | 26259 |
rs565242897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999114 | TTAAAGCATTCCCTC[A/G]ATGTGTTATTAATTT | 26259 |
rs565255008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116911855 | TTAATTTTTGTAACC[A/G]TGCACGTATTCAAAA | 26259 |
rs565266247 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028838 | AAATATTCATTGACT[A/G]AACAGCCATCAAGAT | 26259 |
rs565283750 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941166 | CAGACTGATGGGGGA[C/G]GTCAGCTCTCCACTG | 26259 |
rs565327343 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021127 | GCCACACAGTGCCTC[A/G]TAGGGCATGTTACCA | 26259 |
rs565348744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954498 | TGTTATGAATATTTT[A/G]TGTATAGATGTCTGC | 26259 |
rs565361673 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959155 | GCATCTGCTCAGCTC[C/T]CAGTCCTGCTCCCAG | 26259 |
rs565366214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001784 | TGGTTATCATCTCTT[C/T]GCTGGACTCACTGCT | 26259 |
rs565376909 | in-del | -/T | 0.153665 | 0.230694 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950182 | GTTGTCCTGACATTG[-/T]TTTTTTTTTTTCTCC | 26259 |
rs565388351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991646 | CTAGGGTTTGTGTCT[C/G]TGCCTCTGGCCTGTA | 26259 |
rs565389639 | in-del | -/AA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954131 | AAAAAAAAAAAAAAA[-/AA]AAGAAAAAGCAGTGG | 26259 |
rs565420613 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953416 | CCTCATTTGCTGCTC[G/T]GAAGCTTTGGCTATT | 26259 |
rs565432584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024566 | ATTCAGATCGCCACA[A/T]TTCCTACATTAGCCA | 26259 |
rs565455586 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009728 | TACCTTCTTATTTAC[G/T]TTCATACCCTATGGA | 26259 |
rs565482472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947278 | TTGAGTGAACTGGAG[C/T]GGACTGCAGGCTGAA | 26259 |
rs565486083 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030873 | CCTTTATAAGCCAAC[A/T]TGTATCCAAATTAAG | 26259 |
rs565489768 | snp | A/G | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923063 | ATACAAAAATTAGCT[A/G]GATGTGGTGATGTGT | 26259 |
rs565503149 | in-del | -/GAATT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009614 | GAATTAAGTTGAATT[-/GAATT]AATACTTTTTAAGCA | 26259 |
rs565516215 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972898 | GTTGAAAGTATCACT[A/G]TCTACTAAAAGGAAC | 26259 |
rs565535935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977018 | GACCCGAGAGCCCCA[A/C]CCCAGACATCGGGGC | 26259 |
rs565619594 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916768 | GGCTTAAAACAACCA[C/T]GATTTAGCTCACCAT | 26259 |
rs565626825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923517 | ACTACTGCAAAATTA[G/T]TTTCTTTTTTTTTTT | 26259 |
rs565635983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986560 | GTGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC | 26259 |
rs565641538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987262 | CCGGCTTTGAACTCT[C/T]TGGCATATGGTCAGG | 26259 |
rs565676083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942665 | AGGCGTGAGCCACTG[C/T]GCCTGGCCAAATTTG | 26259 |
rs565697635 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994426 | GCATTCACCTAATTC[A/C]GGGATCAAAAGATAG | 26259 |
rs565702546 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954011 | CCTAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA | 26259 |
rs565741734 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970281 | TAGAGAGAGGAGAGA[C/T]GCGATCTGGTGCATA | 26259 |
rs565748809 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116972740 | GGGGCTGGATTGGAA[C/T]AGGAGGCATCGGTGT | 26259 |
rs565764210 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002563 | AGTCACCTTTGGGAT[A/G]GTGGTGAAAGTCATT | 26259 |
rs565784591 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985494 | TTGGTAACTCCCATT[C/G]ACTCAGAGCTTCCTG | 26259 |
rs565814602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014738 | CGCATGTGCCACATG[G/T]GTTGGCAGTGGTTCA | 26259 |
rs565821670 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938008 | AGAAAGACCATTAGG[C/G]CTTTGGAAAATTCAG | 26259 |
rs565866554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980976 | GACTTTTTTTGTTTT[A/G]TTTTGTCTTATTCAC | 26259 |
rs565866730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972485 | TTGAAAAGCAAAATG[C/T]ATCTGCTTGCCTGCC | 26259 |
rs565885823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116936281 | ATCTGAGGCAGGGTG[C/T]GCCTGTTGTGTTTGA | 26259 |
rs565891684 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116942407 | CGAGACAGAGTCTTG[C/T]GCTGTTGCCCAGGCT | 26259 |
rs565951078 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006662 | AGAGAGGCAGGCCCC[A/G]TCTATGGAGGAGCAG | 26259 |
rs565964386 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922174 | AAGAATATATATTTC[A/G]AGACAAATTGTGGAT | 26259 |
rs565968579 | in-del | -/TG | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999062 | TATCAATTACTGAGT[-/TG]CAGATGAATCCTTCT | 26259 |
rs565985565 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019513 | TGCCTTGTCAGTTAC[A/G]TGGCCTAGCAGGAAG | 26259 |
rs565999531 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971404 | AGGGGGTTTTGGTGT[A/T]TAAGAAATCCTTTTT | 26259 |
rs566004409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973176 | TGATAAAAATAAACA[A/G]ATCAATAAATAAAAA | 26259 |
rs566005174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014405 | CGTTGAGGGTTCCCA[A/G]ACTAGCTTATCTTAG | 26259 |
rs566023158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001221 | GAGTAGAGGCCGTTA[C/T]GCCTTAGGGAGCTGG | 26259 |
rs566028257 | in-del | -/ATTTTATGT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116945080 | GTTTATATTTTTTGC[-/ATTTTATGT]ATTTGTGTATTTTCT | 26259 |
rs566029856 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920171 | TTCCCCCAACTAAAA[A/G]GTTCTTATCCTCAGT | 26259 |
rs566125710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963140 | CTTTATCCCACATGC[A/G]CACTCTCTGGGTGCC | 26259 |
rs566139611 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964102 | CTAAGTGGGCAAAAC[C/T]GGGCAGTGTCGCGCA | 26259 |
rs566145878 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012960 | TATTTTGGGGGTGTG[C/G]GGGGACAGTGAGCTT | 26259 |
rs566159378 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019657 | ATGTATGGGAGTGTA[C/T]ATAAGGTGCGCATAC | 26259 |
rs566168828 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928014 | TCTTTCTTTTTTTTT[C/T]CCCCTCAGAATGAAA | 26259 |
rs566181667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968321 | TTGTATTTTAGTATT[A/T]CAAGTACAAGAAAAT | 26259 |
rs566188991 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970714 | GTAAACAACTACCCC[A/C]CTGCCCCCAACATTG | 26259 |
rs566197314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019629 | ATTATTTTTTAATTA[C/T]GAAACCGAACATATG | 26259 |
rs566266719 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955411 | TATGTTCATAAGTCA[A/C]CAGTCTCTACAGAAT | 26259 |
rs566277415 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915011 | ATCGTCTTCATTTCT[C/T]CCAACAACTCTCTCC | 26259 |
rs566278600 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926086 | AGGCTCCTGTTACTA[A/G]AGGTAAGACTTTTCT | 26259 |
rs566284780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004402 | TTGGATTTTTTAAAT[C/T]GTGAGCTAATACTCA | 26259 |
rs566289432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913849 | ATTTCATGTTGTTGG[A/G]AAAGGCCTTCCCTGT | 26259 |
rs566305244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922178 | ATATATATTTCGAGA[A/C]AAATTGTGGATTATA | 26259 |
rs566342157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956806 | AACCCTGTCTCTACT[A/G]AAAATAGAAAAATTA | 26259 |
rs566342196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949296 | CACTCCCAGCAGATA[C/G]ATGCCAGCCTATTGT | 26259 |
rs566370538 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022357 | CTAAAGAAACTATTA[A/T]AAAAAAAAAAAAACA | 26259 |
rs566384329 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009723 | AGGGGTACCTTCTTA[C/T]TTACTTTCATACCCT | 26259 |
rs566481128 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930944 | TCCCGAGTAGCTGGG[A/C]CTATAGGCTCACGCC | 26259 |
rs566486693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016047 | TAATATTCCCTTGTA[C/T]AGATATACTACATTT | 26259 |
rs566494149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917414 | CAGAAGCTGATCCAC[G/T]TGACATGAATGGGAA | 26259 |
rs566496027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023198 | ACTAGAGTCAGGGCA[C/T]GGGACATGTTTCAGA | 26259 |
rs566539708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016906 | TCTCTCCCCCATTCA[A/G]TTGTCTTGGCACCAC | 26259 |
rs566606857 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023824 | TGCTGGGCAGTACAC[A/C]TACTGCTGGGACAGG | 26259 |
rs566650195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951053 | CTTCTCTGGAGCTCC[C/T]GAAGGGCAGGCCCCC | 26259 |
rs566677140 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984952 | CTATGATAGCACCAC[C/T]GCACTCCAGCCTGGG | 26259 |
rs566703328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919120 | TGTAAGTAACTGATG[C/G]TATGGAAAGCAAAAC | 26259 |
rs566740980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958057 | CTCTGACTCTATTGA[C/T]TGTGATTAACCAAGA | 26259 |
rs566780088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916687 | AGGATCACCTTAGCC[C/T]AGGAGTTTGAGACCA | 26259 |
rs566812247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009827 | GTTTATAGTTCAGTC[C/T]GAAGGAAGCATCCAG | 26259 |
rs566825885 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982083 | TTATCCCAAATACTC[A/C]ATCCAAAAAATAAAA | 26259 |
rs566862321 | snp | C/T | 0.000527652 | 0.0162342 | missense, synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945406 | GAGGATGAGGTGCTG[C/T]GGTACAGGCTGTGCC | 26259 |
rs566876109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015276 | TCTCCTCTGCAATCC[A/G]TCAGCTTGGGTTGAC | 26259 |
rs566887651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117009079 | TCTCAAAAACAAAAA[C/T]AAAAACCTTTGGCTG | 26259 |
rs566890016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913458 | GTCAGTTAACACATA[C/T]TTTGTATCTTCTGTG | 26259 |
rs566915679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116989095 | GAAACTATTAACAGT[G/T]TTTAGGTATCCATCT | 26259 |
rs566939147 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032094 | GCACTTCCGTACAGC[A/G]TCATTTACTATTGTG | 26259 |
rs566958850 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909176 | CAACCATATACTCTA[A/G]TTTTCTACAGTGAAG | 26259 |
rs566959112 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988318 | TTATATCCCCACCAG[C/T]AGTAAGTGGGATCCA | 26259 |
rs566981209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958816 | TCACTCCCCAACCAG[C/T]AGTGATCATGAATAA | 26259 |
rs566987026 | snp | G/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024612 | AAGAATGAAACTACT[G/T]TTTTGCAAGTGCTAT | 26259 |
rs567000037 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950780 | GGTCCAGATACTTGC[A/G]ATTCTGTCCATTAAG | 26259 |
rs567025160 | snp | A/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978682 | TCTAATCAAGAAACC[A/T]CTAAAGACCACAAGA | 26259 |
rs567038129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997569 | GCCTCCTTCACCCCC[A/G]GTCCCCCAGCTTTGG | 26259 |
rs567059710 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947546 | TGAGGTTAGGAGTTC[C/G]ATGGCCAATATGGTG | 26259 |
rs567090021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937115 | GGACAGAAGGAAGAG[A/G]GTCAACAAGGGCTCC | 26259 |
rs567103669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006507 | GATGCTGCGGGGCCC[A/G]CCTGCCCACGGCGGT | 26259 |
rs567140285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962856 | TCGTTCTCAGGGTGT[A/C]ACACTGAGCCCGGTA | 26259 |
rs567155859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989947 | CATGGTGCCTGGCAC[A/G]TGAGAGCTCCCGACC | 26259 |
rs567164641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012711 | ATTATGAGGAGAACT[A/G]TGTCCTTGGCTGTCA | 26259 |
rs567186675 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976094 | TTTTATAACATTTTT[G/T]TAAGTCTGAAATTAT | 26259 |
rs567202943 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032718 | TCACCTTCTCCTACC[A/G]AGCACAACTCCCTGC | 26259 |
rs567220931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000027 | CTCGCTGTCTCCCAG[A/G]CTGGAGCGCAGTGGC | 26259 |
rs567270012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006001 | TTTAAATGGCGGCCA[A/G]CAAATCATCTTCAAT | 26259 |
rs567423861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985537 | CCATAAGTCTAACTA[C/T]AGCCTTACAAAATAG | 26259 |
rs567430930 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994163 | TACTGGTGGTAAAAG[G/T]AGATATGTATTGGTA | 26259 |
rs567449879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986438 | TCGAGACCATCCTGG[C/G]TAACACGGTGAAACC | 26259 |
rs567460185 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019920 | TTAAACAGGAAGTAC[A/G]CACATTCAAAATGGG | 26259 |
rs567494625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993496 | ATGATTAGTGATGTT[A/C]AGCATTGTTTCTTAC | 26259 |
rs567497551 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030218 | ACTACACAGGGGAAC[A/G]GAGCAGATAGAGCTG | 26259 |
rs567503818 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921713 | GTGAAAATATCATGT[A/G]CTCACTGTAGAAATA | 26259 |
rs567529204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025817 | CATCCAGGTCCTCAG[A/G]GATGGCTGCCAGCCC | 26259 |
rs567557138 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019233 | TTATGTATCATCTAT[A/C]CATTATCATCTGTGT | 26259 |
rs567599097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934004 | TGTGGAATTGGCACC[A/G]TGAACTAAATGTATG | 26259 |
rs567610312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920797 | CCCCAAATTCTATAG[C/T]CAATCCTGATGGTGG | 26259 |
rs567613007 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944058 | CTGCTAGGCTGCCGG[-/T]TTTTACAGCTGCTAT | 26259 |
rs567620052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991723 | TATATTTGTTTGTAC[C/T]TGATACAAAACTGGG | 26259 |
rs567674322 | in-del | -/ATTT | 0.0262949 | 0.111607 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923718 | TTAATTAATTAATTA[-/ATTT]ATTTATTTATTTATT | 26259 |
rs567695923 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951774 | TCATGATGGACCCAG[C/T]CATGGTTCTTCCCTA | 26259 |
rs567727655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932613 | CGATCTCGGCTCACT[G/T]CAACCTCTGCCTCCC | 26259 |
rs567743607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995976 | TTAATTCTTTTGCTG[C/T]CTGAATTAAATTCTG | 26259 |
rs567756707 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920407 | TGAGAATATAGCATT[C/G]AACAAGGCAGAAAAA | 26259 |
rs567779860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933166 | CCCAAGAGTTGAAAA[C/T]AAGAGTGTAGCTAAA | 26259 |
rs567802035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984897 | TGGGAGGCTGAAGCA[A/G]GAAGATCACTTAGGC | 26259 |
rs567837086 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003050 | TATCTTTTGTTTTTT[A/G]AAAAGGAGCATCACT | 26259 |
rs567837366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969293 | GTGTTTCCCTGCTCC[C/T]CTCTCATGCTGAGCT | 26259 |
rs567876357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015350 | GTTTTGCTGGCAGTC[A/G]GCAGGAGAGAGGCAG | 26259 |
rs567899978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962126 | TTCAGACACAGGCTA[A/G]CTTGGCCATGAGCTG | 26259 |
rs567901465 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025959 | AGCACTGCCTCTGTC[C/T]CTGTGCGGTCCAGGC | 26259 |
rs567937754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014851 | GGGTTTAGACACAGT[A/T]TTATGGGATCCCTTT | 26259 |
rs567973359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970145 | CACAGCATTAGGGAA[C/T]GGCAGTGTGCTTCGA | 26259 |
rs567978229 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031513 | GAGGTCAGGAGCTCA[A/C]GACCAGCCTGGCCAA | 26259 |
rs567985231 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001615 | TTTCACTCCGTAAGA[C/T]AGATATTATAACCTT | 26259 |
rs567988588 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959581 | AAGCAAAATGGAAAC[A/G]CTGCTGGATACTTAT | 26259 |
rs568068831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981030 | TAGTGCCTTGGTACA[A/G]AACAGGGAGCTCTGT | 26259 |
rs568072602 | snp | C/T | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943333 | ACTCTGGAAATAGAA[C/T]CTTTCTCCCTCTTCA | 26259 |
rs568074551 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935851 | GCCAGGAGCTGAGCT[G/T]TGTCTATGACCTTTG | 26259 |
rs568077973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987372 | AGAGGCGAAAGCCTG[C/T]TGCGAACGGCACCGC | 26259 |
rs568087504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027077 | GATGGGCCAGTCTCT[C/G]TTGCATGTGGCTGAT | 26259 |
rs568091782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971508 | AGAGACTGTATTAGG[A/G]GCTGGAGGAAGTTGT | 26259 |
rs568102376 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029768 | GCGTCCGCTACCACA[A/G]CTGGCTAATTTTTAC | 26259 |
rs568150252 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014085 | ACCTTGTGAAATTTT[-/C]CCAACAGGCCACCAA | 26259 |
rs568174702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925557 | CCTGCCATTTTCCAG[C/T]GGTTACCAACATGGA | 26259 |
rs568176311 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032931 | TGGCAGACACTGGCC[A/G]CCGCAAACCCACTTT | 26259 |
rs568198294 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921746 | TAGGAAATTCAGAAG[A/C]ATAGAAGAAAATAAA | 26259 |
rs568241152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966187 | GCTGTTTCTGTGGTA[C/T]AATTAATATTTCATA | 26259 |
rs568268141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001914 | AAAGCAAAGAGAGAA[A/C]CATATTCTGCTCACT | 26259 |
rs568287375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981844 | GTCTCAAACTCCTGA[C/G]CTCAAGTGATACGCC | 26259 |
rs568308928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993213 | GGTTCAAGCAGTTCT[C/T]CAGCCTTAGCCTCCC | 26259 |
rs568379538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966901 | TTTTTGTATTTTTAC[C/T]AGAGACGGGGTTTCA | 26259 |
rs568400728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979269 | GTTTCATTACCACAC[G/T]CTGGCTGGCCTCCTT | 26259 |
rs568403866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995241 | CCCCTTCTGGGCTTA[C/T]CTGGGACCCATTTGA | 26259 |
rs568419353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922250 | CCCCCAGCCAACCAG[C/T]TTTTTTCTTCTCAAA | 26259 |
rs568487238 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009518 | TTAATGAGGAGCCTT[A/C]TGAATGTGAATTTGA | 26259 |
rs568518929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007595 | AGTGCAGAATATTTT[C/T]TCCGGGATTTGTGCT | 26259 |
rs568542338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014334 | TGTCACTGTCAGTAT[C/T]CCCATGCATTTTACC | 26259 |
rs568569962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961328 | TTAAAGCATTCCAGG[A/C]AAATTTAATGTGCAG | 26259 |
rs568604563 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020679 | GGAGTCTCCATACTC[C/T]GCTCCCTGCCTAGGG | 26259 |
rs568628413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969132 | AGTCTTGTCCTTTGG[A/G]GTTTCACGTCATGGT | 26259 |
rs568694934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950119 | GAAGAAGGGCTTTGG[C/T]CACACATAATCTTCC | 26259 |
rs568701657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915689 | ATAGAGTCTTACCCT[A/G]TAACCTAGGCTGGAG | 26259 |
rs568724591 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002389 | TTTGTGCTGAATTTG[A/T]GCATGGACGGTGCCA | 26259 |
rs568755887 | in-del | -/TAGAG | 0.00716266 | 0.059414 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021582 | TTGAGAAAATTATTA[-/TAGAG]TATTTTGCCTCTAAC | 26259 |
rs568760254 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930057 | ATAGTATTCCATTGT[G/T]TATACATGCCACATT | 26259 |
rs568775816 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928149 | TGTCACCAACAGATG[G/T]TCCAGATTTTCCTAA | 26259 |
rs568793736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919146 | AAAACCGCGGATAAG[G/T]GGGGACGACTGTGTT | 26259 |
rs568821346 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991893 | AGAATATTCTTACAC[A/C/T]GTATGATGCCCACAT | 26259 |
rs568877530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975638 | GGCAGATACCACCTT[A/T]ACCAAGTGATGATAG | 26259 |
rs568895085 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030431 | GCTCGCTGGTGGCCT[C/T]GCTTTAGAAGGTTTT | 26259 |
rs568943161 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909433 | AGGAGTTCAAGACTA[C/G]TCTGGCCAACATGGT | 26259 |
rs568956433 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032390 | CCCAGAAAGCTCTCC[A/G]ACCGGGAGGACGTCT | 26259 |
rs568961649 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032745 | CTGCGCCGGCTGAAC[A/G]CTAGGGTTTCAGCTG | 26259 |
rs569029738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953729 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 26259 |
rs569067185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999824 | CATTCATTCCTGACC[A/G]GGGACTGGCACTAGC | 26259 |
rs569070617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005203 | GGAGTGGAGGAAGGT[A/G]TTAAAGCACTAAAAG | 26259 |
rs569143567 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939466 | GTTTCCTAAGCTCAT[C/T]TGAGCGTGGAATCCT | 26259 |
rs569152925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951705 | CTCTATGTAAATATT[C/G]CTAGTTTGGGGCCAT | 26259 |
rs569231290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026467 | CAGGTCCACCAACAC[C/T]TTCCTTCTGTGGGTG | 26259 |
rs569258241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938717 | TTTGTAATCATTGAG[A/C]ACTGCCTTTGGATTT | 26259 |
rs569322556 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977176 | TGCAGTTTCGCCATC[A/G]TTTAAATCTTTATGT | 26259 |
rs569364661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997737 | GCTGCTGCAGGAGCC[C/G]TGCTGAAACCATACC | 26259 |
rs569366200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027801 | CAAGGCCCGCCCTCT[C/T]GAGTCCTTGCCCTGT | 26259 |
rs569369430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952331 | TGTAACCCTGTCGTT[C/T]AGTGACACGACTGTA | 26259 |
rs569433593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924772 | CAGATCATGCACACT[A/G]ATAAAAGAGGTGTGT | 26259 |
rs569441306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990514 | CTAATTTTTCATCTG[A/G]TATGCTTTCAAGTTT | 26259 |
rs569471445 | snp | C/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982503 | ATATCAGCCCCCCGA[C/G]AAGTGAGGATCTGAT | 26259 |
rs569478646 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023247 | GCTTTTGGGTCAGAC[A/G]TGCGTTTTTAATCTT | 26259 |
rs569515038 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926498 | TCAAGTTGTATCTGG[G/T]CCGAGAGAGAAAGTG | 26259 |
rs569522845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934822 | CTTATTTGTGAATCT[A/G]TGGAACTTTACATGG | 26259 |
rs569523498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023926 | ACTGTCCTTGGCCTG[A/C]GTCTTTCTTGCTCCA | 26259 |
rs569525702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001135 | ACAAAGAGCTCATAT[A/G]TGTAGTGTTTGTTTA | 26259 |
rs569537493 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983367 | AACCTTTTGTGATCC[A/G]CTTATCCCCCAAGTT | 26259 |
rs569559960 | snp | C/T | 9.91457e-05 | 0.0070401 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028044 | CACCGGGGGCTGATC[C/T]GCGCCTATGAGTTTG | 26259 |
rs569585161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117007267 | GATCTCTAAGAAAAA[A/G]AAAAACAGATGAATA | 26259 |
rs569601102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928593 | CCTTTAAACTTTAGG[A/G]TCTCACTCAGTGAGG | 26259 |
rs569628854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116948037 | GGCGATTTGGTTTGG[C/T]ACCTCTTAAGTCAGT | 26259 |
rs569630539 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917014 | TTACAAGAGCAGCAA[A/G]AGGGCGAGCCCCAGT | 26259 |
rs569644854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993625 | GATTTATTTGAGTTC[A/G]TAGTAGATTCTGGAT | 26259 |
rs569662860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928195 | ATAGGACTCTCCGGG[A/G]TAATAGAAATTTACT | 26259 |
rs569664238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956119 | CTCTTTTGGTTTTAA[A/G]AAAAACACCAAGCAA | 26259 |
rs569681866 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949194 | TGAGAGTCCTTATAA[G/T]AATTAACAGGTAAGG | 26259 |
rs569699924 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984976 | GCCTGGGCGAAGAGT[A/G]AGGCACTGTTTCTAA | 26259 |
rs569718178 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956222 | GTTCCTGCCTTTGCT[A/G]GAAGGAGCAGGGCTG | 26259 |
rs569762805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992518 | GTGGGGAAGCTTGTG[C/T]TTTTAGTGTACCTGT | 26259 |
rs569765414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941245 | GTGCCTTCTTGCAAT[A/G]AGGAGATACACCTAG | 26259 |
rs569807300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116972405 | TGTAGCGTTTATTTC[A/G]TTCTGAACCCTAGGG | 26259 |
rs569808176 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996008 | TCTCAGAGGTGGAGG[A/G]TTAGAAGACCGAATT | 26259 |
rs569814473 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979313 | GGGCCTGCTGCAAAC[A/T]GGCATGGGTGCCCAT | 26259 |
rs569843860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020849 | TCAGCAGTGCCCTTA[A/C]AAGGATTTTATCCAG | 26259 |
rs569868444 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966993 | ATGTATTTTAAATTC[-/T]TTTTTTTTTTTAAAG | 26259 |
rs569874138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980045 | CCCAGTTCTTGGGGG[A/G]AGCTGATTCATGGAC | 26259 |
rs569875246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912914 | AATTCGAATATAACA[A/G]TCCTGTGAGGTAGAT | 26259 |
rs569875277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117012907 | GGGAATCAGTTTTAA[C/G]TAGTTTGCAAACATG | 26259 |
rs569890829 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939005 | GAACTGTGGGCCTGA[C/G]TGCCCAGTACATGGT | 26259 |
rs569899466 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938144 | TCTTTTTCTTGTTGA[-/T]TTTTTTTCCTTCAGA | 26259 |
rs569911457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986489 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGCGCCT | 26259 |
rs569917697 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922415 | AAAAATGTTATTGCA[A/G]ATCTCTTCTTTGAAC | 26259 |
rs569918361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019501 | ATTCACTTGGGTTGC[C/T]TTGTCAGTTACATGG | 26259 |
rs569955084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971705 | TTTTTTTAAATCTGT[A/G]CTTTTGTTTTTATGG | 26259 |
rs569964179 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913069 | GTGAACTTGAGTTGG[C/T]ATAAGAATCACTTGA | 26259 |
rs569964216 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955872 | GTAGTGAAGGAGAGC[C/T]ACCTAGTGAAGAGTG | 26259 |
rs570042347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117025308 | CACTGTACTCCAGCC[C/T]GGGTGACAGAATGAA | 26259 |
rs570072092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940196 | GTGTCAGCCTGGGGG[A/G]TGGGCTCCAGTGGTT | 26259 |
rs570076343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932714 | AATTTTTGTATTTTT[A/G]GTAGAGACGGGGTTT | 26259 |
rs570097378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981939 | ATATAACATGTGAAA[C/T]GATACACTATTACTT | 26259 |
rs570108634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921370 | TAAGAGACGAATTGT[C/T]TTTTTGTGGACTGCT | 26259 |
rs570157245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116989038 | CAAATGAAAAGTAAT[C/T]ATTTTCTTTCTCCTC | 26259 |
rs570160666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024868 | AAGGGGTTCAGGCTC[C/T]AACGAAGGAGGAATT | 26259 |
rs570161458 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981055 | CTCTGTAACTACCTG[A/T]TGAATGTATTATTGC | 26259 |
rs570173434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927241 | CTACCAGGATCGTCA[A/G]TGACAGCCTTATCTC | 26259 |
rs570187232 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913045 | CTTTTCAACTCCAAG[C/T]TTCACCACGTGAACT | 26259 |
rs570213118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933220 | CCTGATGCTGTTAGC[C/T]GAAGTCTTGGAACAG | 26259 |
rs570226579 | in-del | -/A | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986625 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGA | 26259 |
rs570269622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010511 | CCAAGGCCCGGCCCC[C/T]ACTGCGCTGCTCACA | 26259 |
rs570281987 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001766 | AGTCATACATTTGCA[C/T]GATGGTTATCATCTC | 26259 |
rs570326951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006609 | CTTAGGACACCAGCT[G/T]CCAGGACATGGCTAG | 26259 |
rs570439048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923952 | TCTCCTGACCTCGTG[A/G]TCCGCCTGCCTCGGC | 26259 |
rs570504756 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011993 | TAATCTAGAGATGGT[G/T]TTTAATGGAGGATGT | 26259 |
rs570507040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964956 | CCCTCCATATGTACA[C/T]GTGGGCACACACACA | 26259 |
rs570518048 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015847 | TCACTCCCCAGTTCC[C/T]TCATCCCCTCCAGCT | 26259 |
rs570578735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917555 | TTCAGAGTCTTCAGT[A/G]TCCATCACTAGAGAG | 26259 |
rs570580364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957883 | GATATTGATAAGTGA[C/T]TAGAGGAGAGCATTA | 26259 |
rs570588367 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960914 | AAGGAGGGGAGGGGA[C/G]GGCCTGTGTTAGACC | 26259 |
rs570595946 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956370 | CCTTTTGAGGCAAGT[A/G]TGCCCAAGTAGATAC | 26259 |
rs570600088 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989712 | AAAGTTTTTGTTTCA[-/T]TTTGGGTTTTTTCCC | 26259 |
rs570607676 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930153 | GTACAGAGATCACTT[G/T]GACAAACTGATTTCA | 26259 |
rs570650721 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921206 | ATTCCATGGACATTT[A/G]TTGTGCATCTACTGT | 26259 |
rs570651968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959006 | TGGCTGCTCTGGGTG[C/T]CTGATCAGAACAGAA | 26259 |
rs570682233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924423 | TTTATTATTTGTGTT[A/G]TAAACATTCAAAATC | 26259 |
rs570710803 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971505 | CACAGAGACTGTATT[A/G]GGGGCTGGAGGAAGT | 26259 |
rs570724100 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910333 | ACTTATATGTGAGAA[C/T]ATACGATGTTTGGTT | 26259 |
rs570724845 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116952382 | TCACTCTTTCAAAGT[A/G]TACAATTCAGTGATT | 26259 |
rs570818602 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014720 | TATGCTGTTTTTGGT[C/G]TGCGCATGTGCCACA | 26259 |
rs570818701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008173 | TATCAGATTTCAGTT[C/T]TTAGATTTACCATCA | 26259 |
rs570829242 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956087 | CACTTTTCTATTCAT[A/G]TGAGAGGACATTTTC | 26259 |
rs570918570 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001306 | GCGGCTTCCCAGTCT[C/T]CCCCTGGGGCTATTT | 26259 |
rs570956566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965962 | GAGATGGAGTTTTGC[C/T]GTGTTGTCCAGACTG | 26259 |
rs570962074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116950892 | TGTGAACTCCGGAAG[A/G]TACTTAGATCATTCC | 26259 |
rs571012990 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976112 | GTCTGAAATTATTTC[-/A]AAAATCAAAAAAGAC | 26259 |
rs571082539 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:117014985 | CCTGCCGGCATCGCC[A/G]CCACCATGCAGCATG | 26259 |
rs571098731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943428 | AATAATTCTCTAATT[C/T]GTATTATTTGTCATG | 26259 |
rs571145511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995580 | TTTCCTCAGTTCCTA[C/T]GTCTTGCCTTGTAAG | 26259 |
rs571152277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010573 | CCTGAGTTCAGCCCC[A/G]ATCCCATAAACACTC | 26259 |
rs571185748 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912336 | GGGACTACACGCATG[C/G]GCCACCACACTCAGC | 26259 |
rs571206193 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932742 | TTTCACCATGTTGGC[C/T]AGGATGGTCTCCATC | 26259 |
rs571207952 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031544 | CATGGCAAAACCCCA[C/T]CTCTACTAAAAATAC | 26259 |
rs571213390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961487 | AGTAGAAAATGAGGC[C/T]GGGGAGAGGGGTGGA | 26259 |
rs571218021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985110 | TTTCCAAGGTATCTC[C/T]GTTAAAAAATTTTCC | 26259 |
rs571218825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011977 | TATTCGCTCTTATAA[C/G]TAATCTAGAGATGGT | 26259 |
rs571254376 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946443 | GGGGCCAGCTAATTC[A/G]TTTTGTGCGGGGCTG | 26259 |
rs571287942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116962062 | AGGGGCCCCTCTCCT[C/T]CTGTACCAGTGACCT | 26259 |
rs571290119 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032826 | GGAAAGGCTGACACC[C/T]CCAAGATGAAGTCCT | 26259 |
rs571309697 | in-del | -/TTTA | 0.0528381 | 0.153711 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013736 | CAGTGGTGTTTTCTT[-/TTTA]TTTATTTATTTATTT | 26259 |
rs571360464 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947920 | GCAGAGCCTGGTCCA[C/T]GCTCAGTGCTCAGGC | 26259 |
rs571391080 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992820 | TTTCTGTATCTACTC[A/T]TTGGTTGATGGCACT | 26259 |
rs571431912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941006 | AAGGGGAAATATGAT[C/T]GCTGTCTTCAGCTAT | 26259 |
rs571451970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999927 | ACTATCTGCCTCTCA[C/T]TGAGCATCAGAGCTC | 26259 |
rs571469742 | snp | C/T | 0.00993419 | 0.0697739 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910554 | TCAATCCTTACTCCC[C/T]TTACCTTACCTTATT | 26259 |
rs571494677 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933322 | CTGTTTAAGAAATCA[C/T]TTCTTTTAACATTGC | 26259 |
rs571523949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990095 | TTTATGTAGGTGTGA[C/T]TGGCTTTGCAAACTA | 26259 |
rs571525866 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912578 | CATTCTCCTGCCTCA[A/G]CCTCCCCAGTAGCTG | 26259 |
rs571526723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024962 | GATGGCGTCACAGAG[A/G]TAGGTAGGTTTACGC | 26259 |
rs571556675 | snp | A/C | 1.74424e-05 | 0.00295312 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945577 | AATAGCCTGCAAGGA[A/C]ATGGGAATCCAAGCT | 26259 |
rs571587953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998292 | TAAATGTCTTTTGTC[C/T]TTATTCACACTTGCC | 26259 |
rs571622050 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938577 | TTCAGCTTCCAACAT[C/T]TTTAAGGTCCGACAT | 26259 |
rs571674163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953033 | GTGAGCCACTGCACC[C/T]GGCCTGTAAGCATCT | 26259 |
rs571725544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990663 | TGGATTTATTCCTGT[A/G]GTAATACAGTTGTAA | 26259 |
rs571754176 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946319 | ACCTCCTAACCTGAT[G/T]AGTGACCAATACGCT | 26259 |
rs571788674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928334 | TCTTTCTGTGACCCA[A/C]GAGCTCTTTTCTCCC | 26259 |
rs571836569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919523 | GCTGGTGCCATTATC[A/G]TTAGTACTCAGAGTT | 26259 |
rs571851054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927652 | ACTTTCTTGGCCGCC[C/T]GCTGCTCACCTTTCC | 26259 |
rs571855275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975769 | AGACAATTGAGAGGC[C/T]TACACAATAAATGAG | 26259 |
rs571868849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968500 | CACACCTGAATGGTA[A/G]TTCCATTGTGTATAA | 26259 |
rs571870227 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969210 | AAGGCTGCAGTGTTT[C/G]CATTGAAATCTTTGA | 26259 |
rs571927077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922485 | GAGATCTTTCATGTC[C/T]TCTTTGCCCTGGAGA | 26259 |
rs571939944 | snp | C/T | 0.00131739 | 0.0256312 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024255 | GATCGTCAGTGGAGG[C/T]GAGGAAGGCCTGGTG | 26259 |
rs571948268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934134 | CCCACAAACCATGCC[A/G]GAGACTGATTTTGCT | 26259 |
rs571971222 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944838 | TGAGTTTTCTGTTAA[C/T]TAAATATATACATAT | 26259 |
rs572005387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020377 | TGTTTGATTCGTGTG[C/G]ATTGAGTCGGCATGC | 26259 |
rs572036731 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978541 | TATTATAAATAGTCA[A/C]CTTCATTCAGTATCT | 26259 |
rs572070780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013301 | AGAGCAAGAGAAAGA[C/T]TGGGGTGGAAACTGA | 26259 |
rs572080846 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967774 | GTCACTTATTCTTTT[G/T]TGTTTGTTTTGAGAT | 26259 |
rs572123621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964496 | ACCATTGTGCTGTGA[A/G]AATGTGAAGCGTGTT | 26259 |
rs572150258 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013756 | TTTATTTATTTATTT[A/T]TTTTTTATTATCATC | 26259 |
rs572173774 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979377 | AAAGACTGGCCATCG[C/T]TACTCATGTCATCGT | 26259 |
rs572221363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914475 | CTACCTGGGAGGCTG[A/G]TGTGGGAGGATTGAT | 26259 |
rs572231361 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943686 | CTGGTCTTTCCTGGG[C/T]ACACACATAGCCCTA | 26259 |
rs572233417 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922060 | GTCTTGAACTCCTGG[C/G]CCCTAATGATCTGTC | 26259 |
rs572242860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963670 | TAGCTACTTCACTAA[C/T]GTGTCACATCATAGA | 26259 |
rs572247438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005732 | AAAGGCAGCTGGAGT[C/G]GACGGAAAAGAAGAG | 26259 |
rs572259602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000695 | AAAACTTCCTAACTG[G/T]GCAAGAGGTTTGAGC | 26259 |
rs572309232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971838 | CCAAGTGACCACCTG[C/T]ATGCCCGTATTGACC | 26259 |
rs572323691 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000149 | ACCACGCCTGCCTTT[A/T]GTATTTTTAGTAGAG | 26259 |
rs572336050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970304 | GGTGCATATTAGCAT[A/G]AGGAAGCCTGGACGG | 26259 |
rs572345279 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993276 | GCCTGGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 26259 |
rs572350407 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008388 | GATTTGGTTATTTCT[A/G]TATACTTACTTGGAA | 26259 |
rs572370451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018985 | ACACTTCCGCTCCCC[C/G]TTTCCCCAATCCTTT | 26259 |
rs572379925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961746 | TGCCATGACGGAGAC[A/G]TCCAGGCTGCCGTGA | 26259 |
rs572380572 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029922 | AGCCCAAAAGCAGTT[A/T]AAAAAAAAAAAAGAC | 26259 |
rs572414682 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029318 | GACTCCAATGCAGAA[C/T]AGTGAGAAATCAACA | 26259 |
rs572422513 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017447 | AGCTTAGGCTAGCTG[C/G]ATTAAACTGGCAGTT | 26259 |
rs572423437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920983 | AGATCCCAGTTTAGA[C/G]TAAAAGGGGGCTCAA | 26259 |
rs572436686 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913118 | GTTCTGGGCCCTCCC[C/T]AGACCTGCTAACTCC | 26259 |
rs572513105 | in-del | -/AG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924778 | ATGCACACTAATAAA[-/AG]AGGTGTGTTTTCAAC | 26259 |
rs572524655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955042 | CTCTTGAAATGGGGG[G/T]GGGGGGCCCTGTATT | 26259 |
rs572549228 | snp | C/G | 0.00349039 | 0.0416295 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116910988 | GGGCGGGACTGTCTC[C/G]TGGCACCCGGTGGAA | 26259 |
rs572578656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003178 | GTGTTCATTTGTATG[C/T]GTGAAGCCTGTCTTT | 26259 |
rs572586145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954603 | ATTCTATATAAGTAT[A/G]TAAAATAAAGAGTTA | 26259 |
rs572614295 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116941320 | GGAGACTGAGACAGC[A/G]TGACACTCTCAGCAT | 26259 |
rs572637790 | in-del | -/TT | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987261 | GCCGGCTTTGAACTC[-/TT]TGGCATATGGTCAGG | 26259 |
rs572641523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993682 | TGCAAATATTTTCTC[C/T]CATTCTGTGGGTTGT | 26259 |
rs572652277 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994179 | AGATATGTATTGGTA[A/C]TGGTGTAAAAGTAGA | 26259 |
rs572665230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947718 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTGT | 26259 |
rs572688206 | snp | A/G | 9.88614e-05 | 0.00703 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985325 | GTGGCCACAGCTTCT[A/G]CTTTTGATGTCGTGA | 26259 |
rs572703908 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116908975 | AAATGCTTTCCTCTT[C/T]TGGCTCTTATCTCTT | 26259 |
rs572715270 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003668 | TTCTTTCTTACAGCA[C/G]CTTCATTTCATCCTT | 26259 |
rs572715359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997241 | CATCTCTGATACTCT[A/G]TACAACTGATGGGTT | 26259 |
rs572752802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027876 | GCTAAGCCGGGGACT[A/G]TGAGTATCTGACGCT | 26259 |
rs572774015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967143 | GGGGGGTCCTGCTCT[A/G]TATACTTCTCTGCAC | 26259 |
rs572778924 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116920202 | GCTGTTCATTTTTTC[-/AT]GTTATTCGTGAATTA | 26259 |
rs572790063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116966566 | AATTGATTTGCAGCC[C/T]ATGTCTCACATCTCG | 26259 |
rs572840465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027591 | CGTGACACATTGCAC[C/G]CTATGGGCTATACCC | 26259 |
rs572882282 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004026 | ATGCTCTGCGTGGAG[C/G]TCAGGGGAGGTGTGC | 26259 |
rs572886291 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909586 | GCGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 26259 |
rs572886322 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934033 | TGCCCTTGGAGAAAA[C/G]CTGTTTGCTTAGATC | 26259 |
rs572895124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917087 | TTGTTATTCTCATGT[A/G]GCCAAGTCCAGAGTC | 26259 |
rs572899828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942273 | CAATCCTCCTGCCTC[A/G]GCCTCCAAAGGTGCT | 26259 |
rs572906697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116989682 | CCTACCAGTGGGACC[A/G]AGGGGGAGAGAGAGA | 26259 |
rs572930086 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032409 | GGGAGGACGTCTAGA[C/T]GGTGCACAGACAGTG | 26259 |
rs572937763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116951984 | CTTTGCTTACTCTAC[A/G]GTCTTACAAATAATT | 26259 |
rs572938140 | in-del | -/TTG | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013900 | GCAGGAAGTAATCAC[-/TTG]TTTTTTTTTTTTGGT | 26259 |
rs572967391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943655 | GTCAGCCAGAGGGGA[C/G]AGGTTAGGGCCTTCT | 26259 |
rs573010429 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981889 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA | 26259 |
rs573090174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937413 | CAAGGATTAGAGGCC[A/G]TGGACATGAGCAGGG | 26259 |
rs573095289 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943710 | AGCCCTATACATTCA[C/G]GTGGCATTCCAGACT | 26259 |
rs573127256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980638 | TTTAAAAAAAAATAC[C/T]TATTTGAGAAGTGAA | 26259 |
rs573131744 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032927 | TAGATGGCAGACACT[A/G]GCCGCCGCAAACCCA | 26259 |
rs573169738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116922934 | AGAGGTGCTTGAGGC[C/T]GGGTGCAGTGGCTCA | 26259 |
rs573203259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116994873 | AGGATCATTTCCTCC[A/G]AGTAGACTTGCTGGG | 26259 |
rs573211209 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001732 | TGAAGGAGGGTGTAA[C/G]GATTTTCAGCTCCCA | 26259 |
rs573221464 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935943 | TTATTTATATAGAGC[C/T]GACTATGTATGTGCG | 26259 |
rs573260585 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031699 | AGCCTGGGCGACAGA[A/G]CGAGACTTCGTCTCA | 26259 |
rs573268191 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031237 | TTCCCACCCCCTTGA[A/G]ATCTTACCTCCCACC | 26259 |
rs573270328 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116999851 | TAGCATCCCCTCTTC[C/G]TCTCCTGTCTTGCCA | 26259 |
rs573291800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002155 | ATGTTTGGCACAGCC[C/T]GCAGCAGTTGGCACT | 26259 |
rs573301222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947109 | GGGCCTGGAGGTGGC[A/T]GAAGTGACGATATTT | 26259 |
rs573303885 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000422 | GCCTGAAAGGCAGTA[A/T]AGGTAGAGCACAGGG | 26259 |
rs573319006 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965417 | AGGTACGAATAGTCT[A/G]AAGTTAGCTTTATCT | 26259 |
rs573331740 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960811 | TACAGTCAAGTTGAG[A/G]AGACGATCAATGCAT | 26259 |
rs573349522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026814 | TCCTAGCTCAGTGCC[A/G]TGACCACAGCCGGTA | 26259 |
rs573374773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940457 | ACAAAGTTAAGAATT[C/T]AGGTATAAAAAATAG | 26259 |
rs573422605 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015040 | CAGCCACAAGAAAGA[A/G]AAAAAAACCTACAAT | 26259 |
rs573437743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939631 | ATGACTTTTACAAAA[C/T]GTTATGGTTTCTACA | 26259 |
rs573462431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027140 | GAATGTACCAGGTTG[C/T]GGGGGCAGATGCCAG | 26259 |
rs573522513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929458 | CAGGCTGGTCTTGAA[C/T]TCCTGACCTCAAGTA | 26259 |
rs573556438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923682 | GCGCCTGCCACCACA[C/T]CCGGCTAATTTTTTG | 26259 |
rs573582846 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920657 | ATACAGAGATCTGGG[A/G]GAGGGGATTCTAGGC | 26259 |
rs573629424 | snp | A/G | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021976 | CCTGATGTTTCACTC[A/G]GATATGTAGTTTTCT | 26259 |
rs573631663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992140 | CTAAGGAAACAAAGC[C/T]GAGTAATTTAGCAAA | 26259 |
rs573651438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932843 | AGCCGTTCTAATCTT[C/T]CTTTGTGAAGCATTT | 26259 |
rs573722302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977420 | ATTTTTACTTTTGTT[A/T]GTGATAGCCTTTCAA | 26259 |
rs573731730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024422 | ATGCCCCCTACCCCC[C/G]GGCTTCGCCAGGTGA | 26259 |
rs573740337 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011761 | GTGCTCAGAGTTTGC[C/T]TGCAGTGTGAACATT | 26259 |
rs573762524 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933372 | TAGAGAGCCATGTGG[C/G]TTTCACATCTGCTGC | 26259 |
rs573769539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992940 | TTTGGGTAGATATCC[A/G]GTAGTGGGATTGCTG | 26259 |
rs573786591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116926426 | AATGAAAGTTTCTTC[A/G]TGAGTGTGGCTTTCC | 26259 |
rs573862930 | in-del | -/GC | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001010 | CCTCAGTTTCTTGAT[-/GC]GCACAAAATGTAGGC | 26259 |
rs573881256 | in-del | -/TTTA | 0.00398564 | 0.0444627 | intron-variant | FBXW8 | GRCh38.p7 | 12:117013737 | CAGTGGTGTTTTCTT[-/TTTA]TTTATTTATTTATTT | 26259 |
rs573893524 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002392 | GTGCTGAATTTGAGC[A/G]TGGACGGTGCCAGAA | 26259 |
rs573914459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983654 | GATACACTGCCAAGA[A/G]AAGGAAAGCAAAAAG | 26259 |
rs573936488 | snp | G/T | 8.24056e-05 | 0.00641841 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028098 | AGCCCTCTCCCTGTC[G/T]GCCGTTCATCCTGTG | 26259 |
rs573963888 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024381 | GGAAGGCAGCACTAA[C/T]CAGCCTGCACCAGGC | 26259 |
rs573964927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921074 | TGGGATTTCCCCCAG[C/T]ACTTGCATTTCTTTA | 26259 |
rs573988767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931284 | GTGTACATTGCTATA[A/G]CTTTGTAGTATATTT | 26259 |
rs574009262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983088 | CCCAGTGAGAGGAGA[C/T]ACACGAGTCTCTGAA | 26259 |
rs574020010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971046 | ACTTTTTTTTTTAAC[A/G]CTAGGAATGCTCACA | 26259 |
rs574030326 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939861 | CATTGGTCTATCCCT[A/G]TCTGTGCTTCATGAT | 26259 |
rs574050537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975264 | CTGTTATAACAAAAC[A/G]GTATAAACTGGGTGA | 26259 |
rs574093202 | in-del | -/TTTT | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019937 | CATTCAAAATGGGCC[-/TTTT]TCAAAAGCAGAGTAG | 26259 |
rs574110387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117020434 | CAGCTGTTAGCTGTC[C/T]GCACTCTGTTTTTCT | 26259 |
rs574133211 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116911551 | AGGGCGATTTTGTTC[C/T]CCCAGATGTGGCAGT | 26259 |
rs574152743 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000109 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGACTACAG | 26259 |
rs574179132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915105 | ACCTACTCCTTCTCT[C/T]CAGGCTGATAAATGA | 26259 |
rs574182717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976083 | CTTTGCATAATTTTT[A/G]TAACATTTTTGTAAG | 26259 |
rs574193489 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944356 | GTCAGTGCTTTATCA[C/G]CTGAGGCCCTTTGTG | 26259 |
rs574206658 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116915580 | CTGACTTCTCTTCCA[-/C]CCAGGGGTAACCACT | 26259 |
rs574211171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954058 | GGCAGAGGTTGCAGT[A/G]AGCTGAGATCGCACC | 26259 |
rs574227347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005455 | TAGAGTTGAAACCTA[C/G]GAGAGTGTTACAACG | 26259 |
rs574275001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961574 | GTGTTAAGATGTAAG[A/G]CTTTATAGAGGGTTC | 26259 |
rs574291241 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954782 | TCTTTGCAATCTAAC[C/G]TTTTGACTTGAAGTC | 26259 |
rs574291689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011617 | TTGTAGTTTTAATCC[C/T]GCATTTTAGTTTTCA | 26259 |
rs574298530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116953327 | CCAGGCTGGGTGTGC[C/G]TGAGTGGAGCCGCTC | 26259 |
rs574352818 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007921 | TGTTTTCTAATCTCT[A/G]TGGTCTTTAACTAAA | 26259 |
rs574366347 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116998984 | TGACTATGATTTATT[A/T]ATTTCCTCCGCACTT | 26259 |
rs574389143 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026645 | CCTCCCAGCACTTAA[C/T]TCTGGGTCACACATT | 26259 |
rs574426092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004858 | CCTGGCTTGAATGCT[C/G]TCTTAACTTCCTGGG | 26259 |
rs574426819 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956385 | GTGCCCAAGTAGATA[C/T]AAAACAAAACTGCCC | 26259 |
rs574508806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002222 | GGTTGCAGGTGCATT[A/G]GCACGTGGTGGTGGG | 26259 |
rs574520256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928885 | GGACGATCTTGGCTC[A/G]CTGCAACCTCTGCCT | 26259 |
rs574528973 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957315 | TCATGCCACTGCACT[A/C]CAGCTTGGTGACAGC | 26259 |
rs574533841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116970778 | ATTGCTTGCGAGAAG[C/G]CTAAGGCAATTGATG | 26259 |
rs574568061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117008637 | TGTATGTTGACAGGA[C/T]TGATTATTTTCAAGG | 26259 |
rs574591683 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964594 | AGTGGCTCTACACCA[A/C]CCGATTCTTACTTGT | 26259 |
rs574696651 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116958153 | TTTTTCAATTGATGC[A/G]TCTTAAGCCCCACTT | 26259 |
rs574704201 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006754 | GGGACTTCTGCATGT[C/T]ACCCAGCGTCCCTGC | 26259 |
rs574707135 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:117001360 | GCCTGCCTGCCCTCT[G/T]CTAGAAGCTTTTGTC | 26259 |
rs574727059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116993891 | TTAGATTTAAGTCTT[C/G]GTTAATTTTTATATA | 26259 |
rs574727945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116965513 | GTATGCCCACCTGTC[A/G]TGCTCCTATCCTCCG | 26259 |
rs574782492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116995637 | ATGGTTTTTTACTTT[C/T]GGACAAAAATGAATT | 26259 |
rs574800496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117006316 | TCATGATTAATTATG[A/G]GGGTGATAGCCCCCA | 26259 |
rs574842772 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116914144 | TAGGTGTGGTGGTGC[A/G]CCCCTTTAGTTCTAG | 26259 |
rs574857579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955671 | TATGTTTATCCTTGA[A/G]GAGAAAGAGTAGAAG | 26259 |
rs574876270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959962 | CAGCTAGTATATTAG[C/T]TGCAGTTGTACTTTG | 26259 |
rs574906229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116913171 | AATCTGATGACTGGT[A/G]TGATCAGGCAAGTTT | 26259 |
rs574938228 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967934 | ACCACGCCCAGCTAA[C/T]TTTTTATATTTTTAG | 26259 |
rs574938310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116959147 | AACAGGTTGCATCTG[C/G]TCAGCTCCCAGTCCT | 26259 |
rs574956301 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030029 | GTACCTACCACATGG[A/G]AACCGTTTGTCCACA | 26259 |
rs574974629 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949338 | ATTGGTGAGCACATA[C/T]TTGCTTTCTATTCTG | 26259 |
rs575068135 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028588 | GAGGGCCTTTGGATG[C/T]GCTTGTTCCTGGCCT | 26259 |
rs575085365 | snp | A/C | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982194 | AACCTTATGAATAAT[A/C]ACAGTAAATATAAAT | 26259 |
rs575128803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116990320 | TGGTTGGGGCATCTC[C/T]GTTGTGTCCTAGCTG | 26259 |
rs575154679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003238 | AAGGGGTAGATACAC[A/G]CAGACATGTACAGTG | 26259 |
rs575160246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935039 | TTTCAGTTTTTTAAT[A/G]TATATTTTAGTGCTT | 26259 |
rs575182724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983730 | ATTTACGGATGATCA[A/G]TAGAAGGGGAATTAG | 26259 |
rs575187744 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983954 | CTCCCCTAAGTCCGT[C/T]AGCTAACAAGTGCTG | 26259 |
rs575242006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116934309 | GTCCCTCGAGGGACT[A/T]AATCTCTCTGTGGGA | 26259 |
rs575265909 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028508 | CAGCTTCTGTGTGTC[C/T]GCCCTCCCAGCTCCA | 26259 |
rs575303807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937191 | CGACAAGTAGCAGAC[C/T]ATGGAAGGAGCATGT | 26259 |
rs575333623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116918622 | AGCTGCAAGTCATGA[A/G]CCTAAATTCCCATTG | 26259 |
rs575376260 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032152 | TTATTTTACAATAAT[G/T]TTTTATTCATTCCTT | 26259 |
rs575413447 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954153 | AAAGCAGTGGTAAAA[A/G]CCATGTTGTTTTGCA | 26259 |
rs575419110 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927649 | CTCACTTTCTTGGCC[A/G]CCTGCTGCTCACCTT | 26259 |
rs575450994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024066 | GTTGTGCATAGACCA[A/G]CACCGTGGAGGGGGA | 26259 |
rs575505893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116938511 | CAAATTTCAGATTGT[A/G]TTATTTAAAATGATT | 26259 |
rs575513335 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003648 | GTCACAAGTGTTTTC[C/T]GTGTTTCTTTCTTAC | 26259 |
rs575552048 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967270 | TACTGCATTATGTGG[C/G]TGTACCATCATTTAT | 26259 |
rs575583632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116932023 | ACATTTCTTCTATAC[C/T]TCATTTATTAAGAGT | 26259 |
rs575611436 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029259 | CCAAGACACTGCACC[C/T]TATGGGCTATACCCT | 26259 |
rs575623199 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116929534 | GCCACTGGGCCTGGA[C/T]TGATTTTTCTTTTTT | 26259 |
rs575643119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939034 | GTTAGTGCCCAAAAC[A/G]TATCTTAACTGATTG | 26259 |
rs575645152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931383 | GTTTTGTGTTTTTAT[A/G]CAAATTTTATCTTTT | 26259 |
rs575658048 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981451 | TTATTATTTAAATAT[A/C]TTTAAAAGATAATTG | 26259 |
rs575660869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116946727 | CTACGGTAATAAACT[C/T]GTCTGGAGGGAGCCC | 26259 |
rs575679924 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988502 | TGAGCATCTTTTCTG[A/T]TGTGTAAGAGCTGTT | 26259 |
rs575705613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927093 | TGCTGTTGGGACACA[C/G]AGTGAAGCTTTTCCT | 26259 |
rs575706205 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002269 | TGCCTACCCAGCGCC[C/T]GGCGACGCTCAGCAA | 26259 |
rs575744649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116996241 | AGGAGGCTGGAATGC[A/G]TGTGACAAGGACGCT | 26259 |
rs575752045 | snp | A/G/T | 6.5893e-05 | 0.0057396 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949622 | TCCTCACGCAGAATC[A/G/T]CAAAGGTGCCGTGAG | 26259 |
rs575762394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022066 | GAAGCTTTCCTCCTT[C/T]TCCTAGGCTGTGGAA | 26259 |
rs575765848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116933573 | AATTCTTCCCTCTAT[G/T]GCCAGTTGGATTTGG | 26259 |
rs575773780 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029754 | AGCTGGGATTACAGG[C/T]GTCCGCTACCACAAC | 26259 |
rs575774805 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976636 | ATTTTTTTTTTTTTT[G/T]TGTATTTTTATTAGA | 26259 |
rs575793487 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973687 | ATGAAACTCAGGGAA[G/T]GTCTTAAGAACTATT | 26259 |
rs575800379 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116923616 | GTAAGCTCTGCCTGC[C/T]GGGTTCACGCCATTC | 26259 |
rs575834368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010241 | GATAAGGATCATGCC[C/T]TCCACGATGGTGAAA | 26259 |
rs575836273 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116974406 | CATGGATTGTTGAGT[A/G]GAATCTTCAGAAGGG | 26259 |
rs575841136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982242 | TAAAAGCAAGACCAA[C/G]TACATGCTGTCTATG | 26259 |
rs575866226 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026167 | CCAGGTCCTCGCCTG[C/T]CTGACAGGGTGCCGT | 26259 |
rs575876714 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930814 | TTTGAACTTATTTTT[A/C]TTTTTTTTATTGAGA | 26259 |
rs575926588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117022649 | GATGGGAGTGAGGCC[C/T]TGTCTTTAAAAAAAA | 26259 |
rs575930699 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010131 | TCTTCCTTTGCATTT[C/G]TTTTTGGCACTCTTA | 26259 |
rs575942380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924113 | TTAATTCCTTTTCCT[C/T]CTTCTTGGAATATCT | 26259 |
rs575943505 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116940523 | CTTCCAGTTTGTGTT[A/G/T]AAAAAAAAAAACCCT | 26259 |
rs575951819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116963529 | GAATTGCTTGAACCT[C/G]GGAGACGGAGGTTGC | 26259 |
rs575993581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117016124 | TATTATAATGCTACT[A/G]TTATCATTTATGTGT | 26259 |
rs575993721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917849 | ATACAATAATTAGCC[A/G]GGTGTGGTGGCACGT | 26259 |
rs576043774 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019090 | ATGCCTAAGGATAGG[G/T]GTCTGTAAACGTGAC | 26259 |
rs576044828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117017239 | ATCATCTTTGTCCAC[C/T]GAATGGACTTGTTAT | 26259 |
rs576054356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015570 | TATCCGTGCTGTGCT[A/G]TGGAGAACCAAGAGT | 26259 |
rs576076851 | snp | A/G/T | 6.59624e-05 | 0.0057426 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985254 | AGTACCCTGTTCATC[A/G/T]TTTTGAGCACGATGC | 26259 |
rs576105636 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116991935 | AGGCACCTCAGCTGC[A/C/G]TGAGCATGGAGTAAT | 26259 |
rs576114438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116911743 | AGAAATCCTGCTCTT[A/G]AAGGCTACCTAAACT | 26259 |
rs576140895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116971013 | CTTGTAAAAGATAGG[A/G]TATGTTCATAAATGT | 26259 |
rs576158072 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018044 | TTATTCAGAGCTCTT[A/C]ACACAGGACCAACCA | 26259 |
rs576160946 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116911867 | ACCGTGCACGTATTC[A/C/T]AAAAAATTATCTCAG | 26259 |
rs576174646 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011287 | TGTCAGATCGTGAGG[C/T]GGGTACTCCTCTGTG | 26259 |
rs576175411 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117019811 | TAAAACACAAAAGCC[A/G]CCTTTATTGCCCTCT | 26259 |
rs576196537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116921119 | ACCTTCTTTCCTTGC[C/T]AGAGTCCCCAGGAGA | 26259 |
rs576211374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985703 | ACTGTGGTTCCTTGG[C/T]CTTCTTCAGACTAAC | 26259 |
rs576225075 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031125 | ATGTCCGTAGTTGTT[A/C]TAATATTAAATGCTT | 26259 |
rs576252230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116912564 | TCCTAGGTTCACGCC[A/C]TTCTCCTGCCTCAGC | 26259 |
rs576360434 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928850 | GAGTTTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 26259 |
rs576427650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976134 | AAAAAAGACTATCAA[A/G]TTACAGGATTAAATA | 26259 |
rs576480472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116969410 | TTTGGTCCCCCTTCA[A/G]TTTAACAGATCGACA | 26259 |
rs576522120 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930764 | TTTCCCATAGTTTTA[C/T]AGTTTCAAGTCTTAT | 26259 |
rs576527975 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116919740 | CTGACTGCGACTTTA[G/T]AAAGGCTCTATGATT | 26259 |
rs576597599 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW8 | GRCh38.p7 | 12:117005621 | TCAGGGTGACCTTGT[C/T]GAAACACCACGTGAT | 26259 |
rs576605113 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000362 | GGAAGTAAGCACTGA[C/T]AGCTGAGTAATACTT | 26259 |
rs576627638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116961018 | GTTCTATCCCCAAAT[C/G]GTCAGATTTATTTGG | 26259 |
rs576628065 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116947653 | CTGAGATTGGAGAAT[C/G/T]GCCTGAACCCTGGAG | 26259 |
rs576638870 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014506 | GTATGTCAAGTAATT[C/T]TGAATTGTGTTCTGG | 26259 |
rs576688221 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013231 | TGGGTGACAGAGCGA[C/G]ACTCCATCATCTCAA | 26259 |
rs576697686 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116911367 | CCTGGTGAGTGGCCG[G/T]CGCCTCCCCCCCGCC | 26259 |
rs576702706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954483 | GTTTTGTTATATGTA[C/T]GTTATGAATATTTTA | 26259 |
rs576724001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116923624 | TGCCTGCCGGGTTCA[C/T]GCCATTCTCCTGGCT | 26259 |
rs576734326 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031747 | TTTAAGCAAAATGAT[A/G]TATAATGAAACTAAT | 26259 |
rs576758559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116973451 | ATCTAACAGGAACCG[C/T]CTTAATAAAGTGATC | 26259 |
rs576804269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116992232 | CTCCAGCTCGGGTAG[A/G]AAGGGATCAGACAGT | 26259 |
rs576818788 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:116956452 | CTTCAGCTGCCAGAC[A/G]TGGCCTGATTCAAAT | 26259 |
rs576838812 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW8 | GRCh38.p7 | 12:116954970 | AACAAACCAATAGCC[C/T]TTTCTTGGCTCGTCC | 26259 |
rs576887083 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031606 | GTAATCACAACTACT[C/T]GGGAGGCTGAGGCAG | 26259 |
rs576927308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117003057 | TGTTTTTTAAAAAGG[A/G]GCATCACTAGTCTTG | 26259 |
rs576985652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117002602 | GTTCACAGATACGGC[C/T]GTGTTACCAAGCCTC | 26259 |
rs577028968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116957470 | TTCTGTTCGGGAACT[A/G]AAGCCCTCAAGGATC | 26259 |
rs577035191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116944833 | TGGCTTGAGTTTTCT[A/G]TTAATTAAATATATA | 26259 |
rs577063469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116997114 | TGGTTAATAATAAAT[A/G]ATAAATACAGTTCTT | 26259 |
rs577092925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116943945 | GACAAGCCTTGAGAA[C/T]AGAGCTTTCTGGCAA | 26259 |
rs577131858 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980547 | TCACAAGTTCACAGT[C/G]TCAGGAGCCAAATCC | 26259 |
rs577177420 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928542 | ACAGAACATGTTTTA[C/G]GTGAAGTCATGTTTT | 26259 |
rs577190558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117000902 | ATGGTCACAAAGTGG[C/T]GCAGGAATGACACGA | 26259 |
rs577233645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942229 | AGATGGGGTCTCACT[A/G]TTCATCAGTGTGGCC | 26259 |
rs577298408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949477 | ATCATCTTTGTCTTT[C/T]TGAATGCCCATGGAA | 26259 |
rs577350154 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026175 | TCGCCTGCCTGACAG[C/G]GTGCCGTCAGTCCTC | 26259 |
rs577372644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116942896 | GATTTTCCTGCATCA[A/G]CCTCCTGAGTAGCTG | 26259 |
rs577381724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976187 | ATTTAATGCCATTTA[A/G]AAACAATGTTACATG | 26259 |
rs577397586 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919596 | ATAAGCCCTTAGCTT[A/C]CGCCTCTTGTGAATC | 26259 |
rs577422335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117021071 | GAAGGATTTCTGCTC[G/T]CCTCAGCTGTCTAGG | 26259 |
rs577496123 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031055 | TGGATGGTGAAACAC[C/G]TGAAGATCTCATATC | 26259 |
rs577511689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117026716 | GTCATGTTTTCTGGG[A/G]CTGCATCTTACCTTC | 26259 |
rs577513296 | snp | A/G | 0 | 0 | intron-variant | FBXW8 | GRCh38.p7 | 12:116955846 | GCAGGGCTAGGTGTC[A/G]TTTGCCATAAGTAGT | 26259 |
rs577518254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116935160 | AAAGTAATAAAGAAA[A/G]AGAGGGAAGATGCAG | 26259 |
rs577527865 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116976838 | TTAGGACAAAAAAAA[A/T]TTATCGGTTTCATAT | 26259 |
rs577554122 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945786 | GGTTGCCAGCCACTT[C/G]CTCTCGGATTGTTAG | 26259 |
rs577571250 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011098 | TTTAGGTTTCTCCCC[A/G]CCTCTTCTTTCCTTG | 26259 |
rs577572149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116939405 | ACTGCTATTCAAAGC[G/T]CAAGTTCTGCAGCGA | 26259 |
rs577591241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928990 | TAATTTTTGTATTTT[C/T]AGTAGAGATGGGATT | 26259 |
rs577599488 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027573 | GAACCCCACCCCCCC[A/C]GCCGTGACACATTGC | 26259 |
rs577622299 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913609 | TTCTCATTGCCTTCA[G/T]GCTGGGTAGGCTGCT | 26259 |
rs577692255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116931104 | CATTCTTCTGTATGT[A/G]GATATCCAGTTCTCA | 26259 |
rs577707830 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116942578 | ATGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 26259 |
rs577714060 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116916542 | TGTAAGGTCTTTAGA[-/T]TTTTTTTTTTTAATT | 26259 |
rs577753976 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116930621 | TCTGTTGATTGTTTC[C/T]TTTGCTGTACAAAAG | 26259 |
rs577759930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027829 | TGTGACACTCACTGC[A/G]CCCATCGGACTTGTG | 26259 |
rs577786272 | snp | A/T | 0.000165126 | 0.0090849 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028175 | TAACCATGTTTAGGG[A/T]TGTGCCTCAGTTGGG | 26259 |
rs577790435 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920384 | GTACCAGCCACTGTT[C/G]CAGGCACTGAGAATA | 26259 |
rs577819220 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117024858 | CTTAGGACTGAAGGG[G/T]TTCAGGCTCCAACGA | 26259 |
rs577828352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117018129 | CCTCTGTTGGAGTCT[C/T]TGGAAGGTTCTGGTG | 26259 |
rs577831902 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:116924893 | TGAATTAGTTACTAA[A/G]CCTTGAATTTACTCT | 26259 |
rs577891525 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022148 | CACTTGTTCTTTTTT[G/T]GCAGGGATTGTTGCC | 26259 |
rs577894561 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028572 | TTACCTCTTTTCCTC[C/T]GAGGGCCTTTGGATG | 26259 |
rs577930794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960086 | TTGTCATTAGGCAGC[A/G]ATAAAGACATCTGGA | 26259 |
rs577936283 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992616 | GCCTCTGCATACCCA[C/T]AGCTTAGCTCCCACT | 26259 |
rs577973836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116937365 | GTGAATGTAAATAGA[A/G]GAGGGGTTCAGGGAT | 26259 |
rs578009725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117015744 | TACAATTCAGTGTTT[C/T]AAGTAGGTCCACAAG | 26259 |
rs578014023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117023300 | CCTTGCTAGATGCTG[A/G]GGTCTTTCTTTTCAG | 26259 |
rs578030418 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116925662 | TTTTTTAAAAAAAGT[A/T]TGGCTGTGTAATGTC | 26259 |
rs578031660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024374 | GGAACAGGGAAGGCA[A/G]CACTAATCAGCCTGC | 26259 |
rs578042548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116974507 | GGAAAGCAAGCCACA[A/G]AAGGATCCAGCCGAT | 26259 |
rs578059633 | in-del | -/TCTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023070 | TTAAAGAAAAAGAAG[-/TCTT]TCTTTATTATGCCTT | 26259 |
rs578085900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116918739 | AAGGTGAGGTCAGCT[C/G]TGCCTAAATTGTGTT | 26259 |
rs578112135 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW8 | GRCh38.p7 | 12:116968060 | AGGCTTGAGCCACCG[C/T]GCCTGGCTTGTCATT | 26259 |
rs578120749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917918 | AATTGCTTGAACCCG[A/G]GAAGCAGAGGTTGCA | 26259 |
rs578145279 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116967521 | GTTTATAGTGTCACC[A/C]AAAGTATGTGAGAGT | 26259 |
rs578148233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116960773 | GAGGCTATGGCACTG[C/T]GGTAGGGCCTTCTTG | 26259 |
rs578153786 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982991 | CAAGTGGCTTTGGAC[C/G]AAGTTGTTTAACCGC | 26259 |
rs578244674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117004043 | CAGGGGAGGTGTGCA[C/T]GAAGGCAGCTTCTCC | 26259 |
rs578245001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW8 | GRCh38.p7 | 12:117011233 | CCCCTCCCCTGGGCC[C/T]GGCCCCGGGCTGCAG | 26259 |
rs578260751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010787 | AAAGCTCACTTTCTA[A/T]TATTAAAAACAGTAA | 26259 |
rs745317043 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987746 | AAACCCCAACCTTTT[A/G]TTTTTTGAATTGCTA | 26259 |
rs745352957 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925693 | GTTTACAAAATTACA[A/G]TTCAATGCTTTGAAA | 26259 |
rs745353097 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000580 | AGTGCCCAGAGCAGC[A/G]GAGGCTGCTAGTCCT | 26259 |
rs745375391 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969015 | GTGCTGCCTTTATAA[C/G]CTTTTAGCTATGAAA | 26259 |
rs745387186 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024178 | CTCCGCAGTGGTAAC[A/G]TCGCCCTGTCGCTCT | 26259 |
rs745431438 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995560 | AGGAAATGTTTGGTA[-/T]TTTTTTTCCTCAGTT | 26259 |
rs745446253 | in-del | -/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017983 | AGAGAGAGAGTGATT[-/G]GGGCGTAAATGTTGC | 26259 |
rs745467892 | in-del | -/TTTTTTTTTC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912178 | TTTTTCCTGTTTTTT[-/TTTTTTTTTC]TTTCTTTCTTTCTTT | 26259 |
rs745473873 | snp | A/G | 8.24151e-05 | 0.00641878 | synonymous-codon, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945474 | CTATTCTTGCTGGAA[A/G]CTCATCTTCCAAGAG | 26259 |
rs745477901 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936808 | GGATAAGAGGAGGAG[A/T]GGACTCAGGATGTGA | 26259 |
rs745543744 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023614 | CACACCCTTATCCCC[A/G]CTCTGCTGTGCTTAT | 26259 |
rs745545808 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982730 | CTGTTGGAAAAATGA[C/T]GCCAGCAAAGCCAAT | 26259 |
rs745627695 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919152 | GCGGATAAGGGGGGA[C/T]GACTGTGTTTTCTGT | 26259 |
rs745640828 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116948986 | TCTCAAAACTTCTGA[C/G]CTCAAGTGATCTTCC | 26259 |
rs745649382 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955011 | CTTGGCAACATTTGG[G/T]GCTGTTGACTTTCCC | 26259 |
rs745651983 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000720 | TTGAGCTCCTTAGGG[-/C]CCCATATTCTCCTGT | 26259 |
rs745679651 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116961099 | CCTCCCAGTTCAAGC[A/G]ATTCTTCTGCCTCAG | 26259 |
rs745698770 | snp | C/T | 1.65847e-05 | 0.0028796 | intron-variant | FBXW8 | GRCh38.p7 | 12:117028021 | ACCATCTTTGTGCTC[C/T]TTCTAGACACCGGGG | 26259 |
rs745702272 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979382 | CTGGCCATCGTTACT[C/T]ATGTCATCGTTAATG | 26259 |
rs745742286 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917940 | GAGGTTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 26259 |
rs745759870 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116918786 | GGGATGGTTTCCTAA[A/G]TAGAGGAAGTGGATG | 26259 |
rs745760991 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004147 | CTCGGTATTCCAGTC[C/T]ACAGTTTCTCTCTCG | 26259 |
rs745766710 | in-del | -/A | 0.000964552 | 0.0219396 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964886 | TCCTCCCTATTAAGG[-/A]AAAAAAAAAAGCTTT | 26259 |
rs745767223 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117005176 | CTTTGTACATACCAG[A/C]AGCAAGATCCAGGAG | 26259 |
rs745808185 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003288 | TTTCATCACCTGTAT[A/C]CTGAGCCCCTCCTAT | 26259 |
rs745843233 | snp | A/G | 3.94625e-05 | 0.00444181 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911061 | CTACAGCCTGGATGA[A/G]TTCCGTCGGCGCTGG | 26259 |
rs745856796 | in-del | -/A | 1.64868e-05 | 0.00287109 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024298 | TATCGGATGAACCAG[-/A]AGCTGTGGGAGGTGT | 26259 |
rs745886678 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928873 | TGGAGTGCAGTGGGA[C/T]GATCTTGGCTCACTG | 26259 |
rs745948318 | snp | A/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984529 | GGATGGCGCTGAGGA[A/T]GGATGTGAAATTCAG | 26259 |
rs745950032 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951886 | GTGAACAGGACCTGG[C/T]GCCTGTCTCCCTGAG | 26259 |
rs745953452 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996705 | GAGAAGTGTAGACAG[A/G]TAACTCGTGGAGACC | 26259 |
rs745968022 | snp | C/T | 3.29468e-05 | 0.00405861 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010373 | CTTGAAGCTGGGTAA[C/T]GTTCTCCGTGACTTC | 26259 |
rs745970931 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959786 | TCCCATTCTTTCAAC[-/A]AAAAAATCAGCTATG | 26259 |
rs745975313 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951091 | CCAGATGCCAGTCCT[C/T]CTCTCTCTGCCTCTC | 26259 |
rs745991543 | in-del | -/TCTG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004101 | CAGATTTCCCATCTC[-/TCTG]TCTGTTGCATTCCGC | 26259 |
rs746020890 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921492 | CTTAGGGGACGATCT[A/G]TATTGCCTGTTGTAG | 26259 |
rs746042440 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008950 | CGGGCGCCTGTAGTC[C/T]CACCTACTCAGGAGG | 26259 |
rs746049377 | snp | A/T | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028066 | ATGAGTTTGCGGTGG[A/T]CCAGCTGGCCTTCCA | 26259 |
rs746076298 | snp | A/G | 1.65302e-05 | 0.00287486 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988864 | TGGGTGTACGAAGGA[A/G]GCAAGGTACACAACT | 26259 |
rs746090062 | in-del | -/AT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971581 | CAGGAGCTTGAAATG[-/AT]ATACATGCTCTGGGT | 26259 |
rs746106260 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983775 | ATATGTTTTATAACA[C/T]AGCAGGAACTATAGA | 26259 |
rs746125495 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963727 | GTTATCTCATCAACT[C/T]GGCAAAGAAACCCTG | 26259 |
rs746137877 | snp | G/T | 0.000115507 | 0.00759869 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010292 | CTGGTGTGTGGAATT[G/T]TGGGCCCACACATTT | 26259 |
rs746143873 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932831 | GCCACTGTGCCCAGC[C/T]GTTCTAATCTTTCTT | 26259 |
rs746200038 | in-del | -/TTG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933593 | GTTGGATTTGGCTTT[-/TTG]TTGTTGTTGTTAACC | 26259 |
rs746205385 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007545 | CCTGGTACTTAAAAG[A/G]AACCATCCTCAACAT | 26259 |
rs746217310 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946278 | TGATAATGACAAATT[C/G]CCTATGTGCCTGTCT | 26259 |
rs746226016 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116931851 | TTTTATTTCTTTCTG[A/T]TGCCTAATTGCTGTG | 26259 |
rs746226487 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977235 | CCATTTATTACTTTC[C/T]TTGAAAGGGAATTAA | 26259 |
rs746242732 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989959 | CACATGAGAGCTCCC[A/G]ACCTGTTAGCTCCTG | 26259 |
rs746246997 | snp | A/C | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975904 | AATTCTGGATTGGAT[A/C]CTGGACCAGAAAAAA | 26259 |
rs746248900 | snp | G/T | 3.29875e-05 | 0.00406112 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985367 | AATGAGGAGGGGTAC[G/T]GGCAGATAGCTGCGG | 26259 |
rs746272167 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030333 | GCTTCCTTTCAACCA[C/G]ATAACTTCCTAAGTG | 26259 |
rs746284063 | in-del | -/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976453 | TTCCAAAGGATCCTT[-/T]TTTTTTTTTTTTTTT | 26259 |
rs746298910 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116945273 | ACTGCCATAAACCCA[A/G]GGCAATAATATAGGT | 26259 |
rs746299913 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019965 | TAGCCTAGAGGGCGA[A/C]GCGCACCCCTCTTCC | 26259 |
rs746328243 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116914673 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTAACC | 26259 |
rs746337161 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912454 | TTGAGAATCATTCTT[-/T]TTTTTTTTTTTTTTT | 26259 |
rs746337973 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944563 | GATCCTGCATTCCCA[A/G]AATGCTGTGCAGACC | 26259 |
rs746338707 | snp | C/T | 1.64798e-05 | 0.00287047 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949758 | GAAGGTCTTTCATTT[C/T]TCTCATACCACCCTC | 26259 |
rs746393061 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956936 | TCATGCCACTGCTCC[C/G]CAGCCTGGGCAACAG | 26259 |
rs746441247 | snp | A/G | 1.66142e-05 | 0.00288216 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024345 | ATTCTAGACACTCTT[A/G]GGAGTTCCTAGTAGG | 26259 |
rs746481283 | in-del | -/TTC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924441 | AACATTCAAAATCTG[-/TTC]TTCTAGCTATTTGAA | 26259 |
rs746490128 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116914824 | AGGTTGTGGTGAGCC[A/G]AGATCGTGCCATTGC | 26259 |
rs746492752 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116958152 | ATTTTTCAATTGATG[C/T]GTCTTAAGCCCCACT | 26259 |
rs746504658 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976452 | TTTCCAAAGGATCCT[-/TT]TTTTTTTTTTTTTTT | 26259 |
rs746521814 | snp | A/G | 3.29636e-05 | 0.00405964 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985272 | TTGAGCACGATGCAA[A/G]AATACAGGCACTAGC | 26259 |
rs746553404 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928915 | TCCCAGGCCCAAGCA[A/G]TTCTCCTGCCTCAGC | 26259 |
rs746568026 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029463 | AAACCCAGGGGATGG[G/T]GCTGGGAGGGGCTGT | 26259 |
rs746607426 | snp | A/G | 3.29614e-05 | 0.00405951 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024186 | TGGTAACATCGCCCT[A/G]TCGCTCTCCGCCCAT | 26259 |
rs746614976 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926557 | AATTAGTTGTGGGAG[A/G]GGATGGAGCCTGACA | 26259 |
rs746728965 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024248 | ACTGGAAGATCGTCA[A/G]TGGAGGCGAGGAAGG | 26259 |
rs746773442 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013102 | ACAAAAATTAGCCAC[G/T]CATGGTGACGCATGC | 26259 |
rs746785516 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950840 | CTGCGATCAACTGAT[A/G]TGCAGCTCCTTTCTA | 26259 |
rs746791948 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976229 | AAGAATGTGCTTGCC[A/G]CTTTTCTGCTGTCTG | 26259 |
rs746792402 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025224 | GACACGTGGCTCACC[C/T]GTAATCCCAGCTACT | 26259 |
rs746793121 | in-del | -/T | 1.66101e-05 | 0.0028818 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024342 | GCATTCTAGACACTC[-/T]TTGGGAGTTCCTAGT | 26259 |
rs746799084 | snp | A/C | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983111 | TCTCTGAAGACTCAG[A/C]AGCTCTATGCAAATG | 26259 |
rs746815415 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982305 | CGAAAAGATGGGAGA[A/G]GTTCTGCATGCTAAC | 26259 |
rs746815419 | snp | A/C | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028129 | ACGCCATGGCCACTC[A/C]CTACTACGACCTCGC | 26259 |
rs746815866 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116949919 | TGGTGTAGAGCGGAT[C/T]TGTGATCCATTTGTC | 26259 |
rs746817469 | snp | C/T | 1.64914e-05 | 0.00287149 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010309 | GGGCCCACACATTTC[C/T]CTTCCTCTCTCAGAT | 26259 |
rs746828004 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003080 | TAGTCTTGTATGTGA[A/C]GATCTGTACTGAATA | 26259 |
rs746834140 | in-del | -/TGCAAATGGGAGT | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983119 | GACTCAGAAGCTCTA[-/TGCAAATGGGAGT]TTTTTTTCTCTTTAC | 26259 |
rs746889988 | snp | A/G | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985342 | TTTTGATGTCGTGAT[A/G]TTATCCCCCAATGAG | 26259 |
rs746909120 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994322 | GTGTGAAAGTATGGT[A/G]CTGGTGTAAAAGTAA | 26259 |
rs746920982 | in-del | -/TG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001035 | GTAGGCAGTAGTATT[-/TG]TCTTCTCTCCCTCTT | 26259 |
rs746976732 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021148 | CATGTTACCAAACTT[C/T]ACCTTTGCTGGGTAG | 26259 |
rs746979946 | snp | G/T | 1.65979e-05 | 0.00288074 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928078 | CTTACGAATTGGCAA[G/T]CAATATATTTCAGTA | 26259 |
rs746996217 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962039 | GTAGTGGGCCACAGC[A/G]GTGTTGAAGGGGCCC | 26259 |
rs747031925 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919315 | TCTTGGCTATGGGGC[C/T]GGGCTCTGCAGTCAA | 26259 |
rs747077741 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987008 | TTTGAGTGAAAGGTT[C/T]CCACAAAATGCTCTG | 26259 |
rs747086733 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116957501 | GTGTTTCCAACACTC[A/G]CTTAGTTTTATATGT | 26259 |
rs747107370 | snp | A/G | 3.29527e-05 | 0.00405898 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964744 | CCCGCACCTGGGACT[A/G]CGTAGCCCCCTTCCT | 26259 |
rs747130523 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026837 | AGCCGGTACTGCATG[A/G]AAGTTTCAGAATGAA | 26259 |
rs747163232 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939354 | ATAAGGGATACTCAA[C/T]GTGTATCCCCTTCTT | 26259 |
rs747168879 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027718 | GCGAGTCCACGCTGT[C/T]GGCTGTACAGAGAGG | 26259 |
rs747189414 | snp | G/T | 1.64735e-05 | 0.00286993 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010378 | AGCTGGGTAACGTTC[G/T]CCGTGACTTCACGTG | 26259 |
rs747242848 | snp | A/C | 3.30017e-05 | 0.00406199 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964658 | CATAGCCCTGCTCTT[A/C]AATCTCCTTTTGGAA | 26259 |
rs747284950 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966349 | GTTTTAGGATCATCT[A/G]ATAGCCTTTCCCTAC | 26259 |
rs747303532 | snp | C/G | 0.000115553 | 0.00760019 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964785 | GACGAGGAGGATGAG[C/G]CTGGAATGCAGCCAA | 26259 |
rs747316588 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117010214 | GGCAGAACATCTTCA[C/T]GGGAGCTCAGTGATA | 26259 |
rs747375127 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996764 | CTCCCAAAGGGTCCA[C/T]TGTTGTTGTGAGGGT | 26259 |
rs747377205 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921611 | AACAGCACCTCCCTC[C/T]CCCTAGCACCTGGTG | 26259 |
rs747379157 | snp | A/T | 1.65184e-05 | 0.00287384 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945385 | AAGACGTGGAAGGTG[A/T]TTGCAGAGGATGAGG | 26259 |
rs747385346 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944574 | CCCAGAATGCTGTGC[A/G]GACCGGGATCACGCT | 26259 |
rs747418315 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978811 | AGAGTATACCAATTG[C/T]GTTTTTTTTCCAAAA | 26259 |
rs747461065 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021080 | CTGCTCGCCTCAGCT[A/G]TCTAGGAGTACCTAC | 26259 |
rs747461359 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994985 | GCATCCCCTTCCCCT[A/G]GTGGTTCTTGGACGG | 26259 |
rs747469040 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009096 | AAAACCTTTGGCTGG[C/G]TGCAGTGGCTCAGGC | 26259 |
rs747476608 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933086 | TTAAGCATGAGTACC[C/T]ATATTGTTTTCTTTC | 26259 |
rs747525099 | snp | C/T | 3.30688e-05 | 0.00406612 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027472 | GACGGTAATGCGAAA[C/T]GCCGACCTGGACAGC | 26259 |
rs747547263 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030462 | CATCAAGCCCCGCCC[A/T]TTCTCTCTCATAGTC | 26259 |
rs747591570 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990782 | CTCTCAAAATTTCCA[A/G]CTCAACTAAAAGCAT | 26259 |
rs747600838 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978993 | TTGGCTTTGTGCACA[C/T]AAACAGAAGCAGCTA | 26259 |
rs747611900 | snp | C/T | 1.65214e-05 | 0.0028741 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988643 | ATTTATGGGACTAAA[C/T]AACTCTTACCTTTTA | 26259 |
rs747619166 | snp | C/G | 3.31071e-05 | 0.00406847 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988615 | TTGCATATTTTTGAT[C/G]AAGTCAGGATGAATT | 26259 |
rs747626804 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022142 | CAAAGTCACTTGTTC[C/T]TTTTTTGCAGGGATT | 26259 |
rs747674137 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031355 | ACATGGTACAGTAAC[A/T]CTTCACCAACCGTCA | 26259 |
rs747685248 | snp | C/T | 1.6596e-05 | 0.00288058 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928084 | AATTGGCAATCAATA[C/T]ATTTCAGTATCTGGA | 26259 |
rs747695573 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959750 | AATCCCTCTGTCGTG[C/T]AGAGCTTGAGAGAGG | 26259 |
rs747756050 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973177 | GATAAAAATAAACAG[A/C]TCAATAAATAAAAAG | 26259 |
rs747757262 | snp | A/G | 1.65493e-05 | 0.00287652 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024326 | TGTATTCCGGGTAAG[A/G]TGCATTCTAGACACT | 26259 |
rs747810991 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000700 | TTCCTAACTGGGCAA[A/G]AGGTTTGAGCTCCTT | 26259 |
rs747848925 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116972339 | CAAGGAAGATAAATC[A/G]AATTTTAAGTGAGAG | 26259 |
rs747865978 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116911932 | GCACTTTCATTAGGA[C/T]AGAGTTTCTTATCTT | 26259 |
rs747870261 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926696 | TTGATTTAACATTCT[G/T]TTCCTTCTCTTTGCC | 26259 |
rs747887387 | in-del | -/GTGGGCA | 6.69198e-05 | 0.00578407 | splice-donor-variant | FBXW8 | GRCh38.p7 | 12:116945529 | CGAACCAACTGGAAG[-/GTGGGCA]GTGGCCAATATCATT | 26259 |
rs747899436 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927284 | CGTTACCTCATCTCT[A/G]ATTGCTTATCCAAAG | 26259 |
rs747932392 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939125 | TACTCGTTGCAAAAA[G/T]AAGTCAGGAACCAAA | 26259 |
rs747934295 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001805 | ACTCACTGCTCTGAC[A/G]TGAATATTCCCTGTT | 26259 |
rs747935406 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970926 | TCTAGTCTTCATATT[C/T]AGACACTTTGCAAAC | 26259 |
rs747953428 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117015258 | CACTTCCATGGGTTT[C/G]ACTCTCCTCTGCAAT | 26259 |
rs747960580 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014357 | ATTTTACCTTTACCT[C/T]GTGGAATATAGCTAC | 26259 |
rs747978739 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025351 | CAAAACCGAGATGAT[A/T]CTGGGCCAGTGGCCT | 26259 |
rs747991127 | snp | A/G | 4.99671e-05 | 0.00499811 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945364 | CTTCTGCTGTTTTAG[A/G]TGAGCAAGACGTGGA | 26259 |
rs747995428 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996419 | CTTAGGAATCAGAAA[C/T]GCAGTGCGCATAGAT | 26259 |
rs748000096 | snp | C/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909844 | TGTTTCTTGAGTGGA[C/G]GTTGGAAGATTAAGT | 26259 |
rs748005065 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026134 | GTACCTCCCGCTGTC[C/T]GCTTCAGTCTCTTCA | 26259 |
rs748057220 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938111 | CCTTTAACATTTGCT[C/T]GTGAAAGTTTAACTA | 26259 |
rs748081989 | snp | A/C | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983177 | AAACAAATGCAAACA[A/C]ATGCAATGCAGAGTG | 26259 |
rs748108104 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950997 | GCAAAAGAACTTAAA[A/C]ATAAAGGAGAGCCTT | 26259 |
rs748143896 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921324 | CCTTTTGCTCTTCCT[C/T]ATAGCTAGGCATGGG | 26259 |
rs748167564 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116961185 | ATTTTTAGTAGAGAC[A/G]AGGTTTCACCCTGTT | 26259 |
rs748200945 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929884 | TTCTACTCTCTACTT[C/G]TATGAGCTCAACTTT | 26259 |
rs748225803 | snp | A/G | 6.07589e-05 | 0.00551142 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911000 | CTCGTGGCACCCGGT[A/G]GAACCGAGGAGAACG | 26259 |
rs748235317 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117005594 | AAGAGCCGGAAGAAG[A/G]TAAGACACAGGTCAG | 26259 |
rs748257482 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116974103 | CCTAAACAGAGTCTG[A/G]TGGCCTCCCTGACTT | 26259 |
rs748263044 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017457 | AGCTGCATTAAACTG[G/T]CAGTTCTACCTGAAA | 26259 |
rs748274317 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988262 | TCATTTGGTATTTTG[A/G]TAAGAGTAGCCAAAG | 26259 |
rs748289517 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025113 | TGGCCCTGCAGGCCT[C/T]GAACAGGAGACCCTG | 26259 |
rs748317810 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964753 | GGGACTACGTAGCCC[C/T]CTTCCTGGAATCAGA | 26259 |
rs748321300 | in-del | -/AAAGC/AAGA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947751 | AAAAAAAAAAAAAAA[-/AAAGC/AAGA]AAAGAAAAGAAAGAA | 26259 |
rs748327555 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018466 | TGCTGAGCTGACGAC[A/G]GGCTTTGCCAAGGCG | 26259 |
rs748328559 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955545 | GTGTTTTAGCACAGA[A/G]TTTGTCTAGAAAGTT | 26259 |
rs748378970 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116940626 | GTTTTAAGCTGATTA[A/G]CAATCTTTTCTTTTG | 26259 |
rs748438546 | in-del | -/AGAGT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019945 | ATGGGCCTCAAAAGC[-/AGAGT]AGAGTAGCCTAGAGG | 26259 |
rs748455020 | snp | G/T | 1.64893e-05 | 0.0028713 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949571 | ATGCTTGGCTTTCGG[G/T]CTGTCCCGAGAGCAG | 26259 |
rs748496267 | snp | A/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909474 | CTCTACTAAAAATAC[A/G]AAAACTTAGCCAGGT | 26259 |
rs748520791 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939547 | TTTGGTCCATGTAAT[C/T]AAAGAATGGCTACAT | 26259 |
rs748538101 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954297 | TTTTTTCATAGTGTG[A/G]CTGTAGCCTTTGTTA | 26259 |
rs748548220 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998080 | TTCCTTAGCCTCCCA[A/G]AGTGCTGGGATTACA | 26259 |
rs748604158 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116934653 | TATTATAAATTCATA[A/G]GAAGTTGCAAAAAAT | 26259 |
rs748614891 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116923192 | GACTGGGCGACAGAG[C/T]GAGACTCTGTCTCAA | 26259 |
rs748618715 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013409 | TGCATAGGAGTTTTA[C/T]CAGTGTAGATCAATG | 26259 |
rs748649049 | snp | A/T | 1.6477e-05 | 0.00287024 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988817 | TAGACGTCTCGGCCA[A/T]CCAAGTTGCTTTTGG | 26259 |
rs748718588 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017405 | CTAAACTTCAGAGAT[-/A]ACAGCCTTAAAATAC | 26259 |
rs748743429 | in-del | -/TAAATA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116972770 | TGGAATTTATGGTGT[-/TAAATA]TAGATAGAGAAGTAA | 26259 |
rs748745398 | snp | A/G | 0.000197742 | 0.00994143 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945461 | GCAGCATCTCTGACT[A/G]TTCTTGCTGGAAGCT | 26259 |
rs748755801 | in-del | -/TGAA | 1.64754e-05 | 0.00287009 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949741 | TGAGTGCTCTGCATC[-/TGAA]TGAAGGTCTTTCATT | 26259 |
rs748804753 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023356 | ACTTGCATCACAGGG[C/T]CTCTTAAGCTCATCT | 26259 |
rs748804971 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981900 | ATTACAGGCATGAGC[C/T]ACCACACCCAGCCTA | 26259 |
rs748837791 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116911618 | TATGTGTGCATGTTA[C/T]TGGGCATCTAGTGGG | 26259 |
rs748855597 | in-del | -/TCG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969449 | TTTACACTAACATTT[-/TCG]TGAATAGCTACTTTT | 26259 |
rs748880608 | snp | A/G | | | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032505 | ATTCAAGGACCCACT[A/G]TGTGTGAAATGGTGC | 26259 |
rs748900112 | snp | A/G | 1.65416e-05 | 0.00287586 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988627 | GATCAAGTCAGGATG[A/G]ATTTATGGGACTAAA | 26259 |
rs748900116 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116948562 | CTACCACTTATTGAA[C/G]ACTTGCTGTATGTTA | 26259 |
rs748903645 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022172 | TGTTGCCCCTTGCTG[C/G]CTTCCTCAGGCTGCT | 26259 |
rs748964330 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019105 | TGTCTGTAAACGTGA[C/G]AGAGAGAGACCTTTG | 26259 |
rs748982780 | snp | G/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031382 | GTCATCAATAGGTTT[G/T]CTTAGAAACTACAAC | 26259 |
rs748993535 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012588 | GAGGGAAGTCTTACA[-/T]TTTTTTCCCCGGAGG | 26259 |
rs748998051 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960952 | GTTGGTAGGATTGGG[C/T]TGGGTTGGTGATTCT | 26259 |
rs749008992 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116916318 | GTTTTCTCACTTTTG[A/T]TAGTAACTTGTGTAT | 26259 |
rs749009331 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917563 | CTTCAGTATCCATCA[C/T]TAGAGAGAGAACAAC | 26259 |
rs749015243 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991370 | GAATTTTTAAGAAAC[A/G]TAATTGTCATATAAC | 26259 |
rs749015448 | snp | A/G | 1.64917e-05 | 0.00287151 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028145 | CTACTACGACCTCGC[A/G]CTGGCCTTTCCCTAT | 26259 |
rs749060822 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928789 | GATTCAGATTCAGGA[A/G]GTCTGCGGTGGGGCC | 26259 |
rs749077857 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116957294 | AGAGGTTGCAGTGAG[C/T]CAGGATCATGCCACT | 26259 |
rs749117145 | snp | A/G | 4.51325e-05 | 0.00475018 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985168 | GAACATATTAAGTAA[A/G]TTTAAAATTGTTACC | 26259 |
rs749151019 | snp | G/T | 1.65059e-05 | 0.00287275 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010501 | ATGGCTTCTGCCAAG[G/T]CCCGGCCCCCACTGC | 26259 |
rs749202506 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955579 | TGATAGTAAGTGCTC[A/C]GGAAACATGTCTTTT | 26259 |
rs749225875 | snp | G/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985193 | GTTACCTGCATTGTT[G/T]CTTGCTGCATAGGGT | 26259 |
rs749243107 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939302 | GAATAATGCAAACGT[C/G]TGAAATCCAAAATAC | 26259 |
rs749244257 | snp | G/T | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964770 | TTCCTGGAATCAGAG[G/T]ACGAGGAGGATGAGC | 26259 |
rs749271397 | snp | C/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909311 | AGAAGAGTTAGACAA[C/G]GAATAAGGGACAGTT | 26259 |
rs749288434 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971024 | TAGGGTATGTTCATA[A/T]ATGTAAACTTTTTTT | 26259 |
rs749308734 | in-del | -/GGGCTCGGCGGCCGGAGGT | 0.000430674 | 0.014668 | splice-donor-variant, frameshift-variant, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116911141 | AGGCTGCCGAGAGGC[-/GGGCTCGGCGGCCGGAGGT]GGGCTCCGGGCGCGG | 26259 |
rs749325133 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963673 | CTACTTCACTAATGT[G/T]TCACATCATAGATTT | 26259 |
rs749351471 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962272 | TTCCTGCCCTCACTC[C/T]CTTCTCTTTCTCTGA | 26259 |
rs749358084 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008755 | AGAAACGCACATCAC[C/T]CTCATGTGTGTGCTG | 26259 |
rs749374143 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950388 | TGTATACTTAATGCC[A/G]TAAAGTAGAAAGCAG | 26259 |
rs749394927 | snp | C/T | 1.64827e-05 | 0.00287073 | stop-gained, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988837 | GTTGCTTTTGGTGTA[C/T]AGGGTCTGGGATGGG | 26259 |
rs749446009 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007350 | TGCCTTCTAGGTCTA[C/T]CTGCAAGCCAAAGAG | 26259 |
rs749460516 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919365 | CTGGCTCTGCTGTTA[A/C]CAGTTTGCCTTGGGC | 26259 |
rs749465020 | snp | G/T | 3.75566e-05 | 0.00433323 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911044 | GCGGCGAATATGGAC[G/T]ACTACAGCCTGGATG | 26259 |
rs749478119 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944361 | TGCTTTATCAGCTGA[A/G]GCCCTTTGTGCAGTA | 26259 |
rs749495346 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025049 | CAGCAGCCCAGCCCA[A/G]GGCTGGCTCATCAGA | 26259 |
rs749500852 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029190 | GGCCACAAAGAACAG[C/T]TCAGATGCACAAAGA | 26259 |
rs749527469 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989606 | TTTATCACTCCCTAG[C/T]ATGTTACTATCCTGA | 26259 |
rs749535752 | in-del | -/TT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116999123 | TCCCTCGATGTGTTA[-/TT]AATTTACAGGGTAAA | 26259 |
rs749536061 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953051 | CTGTAAGCATCTTTT[-/A]AAAACCATGAGTGGT | 26259 |
rs749546892 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913406 | CCCAAAACTTAACTA[C/T]GAATAGCCTACTGTT | 26259 |
rs749554712 | snp | C/T | 1.81361e-05 | 0.00301127 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928002 | AAATTATAAACTTCT[C/T]TCTTTTTTTTTTCCC | 26259 |
rs749602951 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956774 | GGAGTTTGAGACCAG[C/T]CTGGCTAACATGGTG | 26259 |
rs749640895 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018782 | CATCCATGCTGGTAT[C/T]TAAATACAATAGGAA | 26259 |
rs749650153 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116942870 | GCAACCTCTGCCTCC[C/T]GGGTTCAAATGATTT | 26259 |
rs749665364 | snp | C/T | 3.29554e-05 | 0.00405914 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024265 | GGAGGCGAGGAAGGC[C/T]TGGTGTCCGTGTGGG | 26259 |
rs749673736 | in-del | -/TGTATCACATTTTC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992795 | GTGTGTGTGTGTGTG[-/TGTATCACATTTTC]TGTATCTACTCATTG | 26259 |
rs749701503 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955801 | CAGATGACATCATGA[A/G]TTCAAAAAAGACAGT | 26259 |
rs749704294 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913253 | CAAGGCTTTCCATTT[A/G]TAACACCTTAGAGGT | 26259 |
rs749719868 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013223 | CTCCAGCCTGGGTGA[C/T]AGAGCGAGACTCCAT | 26259 |
rs749730414 | in-del | -/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020742 | CTGAGCCTGGCGCTT[-/G]GCCAGCAGCCTCCCC | 26259 |
rs749746868 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116999162 | TGTAGAGAGCAAAGG[A/T]AAACTCCTGCTCAGC | 26259 |
rs749757786 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912041 | AGTTGGGAAAATCAA[A/G]AACACCTGAAATGCA | 26259 |
rs749773965 | snp | G/T | 6.60229e-05 | 0.00574518 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010286 | GTCGGCCTGGTGTGT[G/T]GAATTGTGGGCCCAC | 26259 |
rs749817465 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025851 | CTCCAGTAGATCTCA[-/T]TTTTTCTCTCAGCAA | 26259 |
rs749830513 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924569 | AACCAACCTCTGTCT[G/T]ATAGTGTGTTTTAGA | 26259 |
rs749859803 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968132 | TGTGAACAATGTTAA[C/T]TTTTTAATCTAAAAG | 26259 |
rs749863935 | snp | A/G | 4.94173e-05 | 0.00497053 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949673 | ACACAGTTTTGTGTG[A/G]TGTGCATTCTCACGA | 26259 |
rs749906012 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937511 | GACCATGGGATAAAT[A/G]TTTTCCAGGAGGAGA | 26259 |
rs749918174 | snp | C/T | 3.29462e-05 | 0.00405857 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949623 | CCTCACGCAGAATCG[C/T]AAAGGTGCCGTGAGC | 26259 |
rs749927160 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014103 | AACAGGCCACCAAAG[C/G]TCTGTTCATGTTCTT | 26259 |
rs749933312 | in-del | -/CT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935632 | GGAAAGGCAAAATCA[-/CT]CTAAAAAACAGATTG | 26259 |
rs749933641 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025685 | TGTTGAGGGCGCCTC[A/G]GCCCTTTTTCTGAAT | 26259 |
rs749957001 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996196 | CACACGGCGTGCATC[C/T]TAATCAGGGAGCTGT | 26259 |
rs749990138 | in-del | -/GTAGACCACTGGTCCTAAACTCCA | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984229 | AAAGCATAAGCTCCT[-/GTAGACCACTGGTCCTAAACTCCA]GTAGACCACTGGTCC | 26259 |
rs750036381 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956717 | TCATGCCTGTACTCC[C/T]AGCACTTTGGGAGGC | 26259 |
rs750079388 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988898 | AAGATATATAATTAA[C/T]AAAAAAGAATATAGA | 26259 |
rs750106018 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963108 | AGGTTCAGAAAGCAC[A/G]TCTCTCCCGTTTGGC | 26259 |
rs750112649 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995276 | GAGCCCACAATTCTT[G/T]TAATCTGACCTGCCT | 26259 |
rs750114626 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007958 | GGTAAAGGTACTCTT[C/G]AGATAGTTCGGATTC | 26259 |
rs750114718 | snp | G/T | 3.29766e-05 | 0.00406045 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949567 | CACGATGCTTGGCTT[G/T]CGGGCTGTCCCGAGA | 26259 |
rs750156203 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920020 | GCAAACCAAACCAAA[C/T]GTGTACTCATGAATT | 26259 |
rs750201516 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116931042 | CGAACTCCTGGCTTC[A/G]AGTAAGAGTTCACTT | 26259 |
rs750209777 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116923916 | GACGGGGTTTCACCA[C/T]GTTAGCCAGGATGAT | 26259 |
rs750214661 | in-del | -/TTTTTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915642 | ACTCACCTGACTACT[-/TTTTTT]TTTTTTTTTTTTTTT | 26259 |
rs750234064 | snp | C/T | 3.4323e-05 | 0.0041425 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027346 | CTGCGGCAGCAAGTG[C/T]AGGCCCAGTGGACGC | 26259 |
rs750237899 | snp | G/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985333 | AGCTTCTGCTTTTGA[G/T]GTCGTGATGTTATCC | 26259 |
rs750238720 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019653 | ACATATGTATGGGAG[C/T]GTATATAAGGTGCGC | 26259 |
rs750263323 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943883 | TACTATTTTGGGTAA[A/G]TGCCCTGGAGATAGG | 26259 |
rs750272709 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989501 | AATTCACATTCTTAC[C/T]AACAGTGCATAAAAG | 26259 |
rs750328960 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941907 | AATACCCACCTAATT[C/G]CAGTAGTGCACCAAA | 26259 |
rs750330221 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028741 | CCATGGTTTATAATT[A/G]TATACTTATACAGTT | 26259 |
rs750367064 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913940 | TACTAGGTTCTCTAT[A/G]AGTAGCATACAACTT | 26259 |
rs750374420 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024771 | CTGCTGTCCTCCACT[C/T]GAGTCCGTCATGTGT | 26259 |
rs750387391 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990265 | CCTTGTGCTGCAAAC[-/T]TTTATCATCTCATTT | 26259 |
rs750426891 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117015155 | GCTTCTTGCACCACC[-/A]CACAGTTCTGCATGT | 26259 |
rs750432306 | snp | A/G | 0.000363192 | 0.0134709 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024312 | GAAGCTGTGGGAGGT[A/G]TATTCCGGGTAAGGT | 26259 |
rs750434143 | snp | C/G | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988049 | CTTCCCTCTAGGACT[C/G]CATGGTATTCCAGCG | 26259 |
rs750437056 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935636 | AGGCAAAATCACTCT[A/T]AAAAACAGATTGGGA | 26259 |
rs750459954 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010906 | TGATGGAAGGAAAGA[A/G]AGACTTCATGTGAAC | 26259 |
rs750472620 | in-del | -/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981924 | AGCCTAAAGTTCTTA[-/T]TATAACATGTGAAAT | 26259 |
rs750553205 | snp | A/C/T | 0.000149448 | 0.00864317 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928069 | TCCAACTGCCTTACG[A/C/T]ATTGGCAATCAATAT | 26259 |
rs750569185 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988314 | AAGATTATATCCCCA[C/T]CAGCAGTAAGTGGGA | 26259 |
rs750580440 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951921 | GTTTTTCCAGTGGGG[-/A]AACATTCTTTCCAAA | 26259 |
rs750596806 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032125 | CATTTGTATGGTTAT[A/G]GGAGGCAATTTTTAT | 26259 |
rs750607345 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021879 | GTGACGTTTCATCCC[A/G]TTGCTTTCGGCTTCC | 26259 |
rs750624303 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013156 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 26259 |
rs750692369 | snp | A/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978626 | CTTCAGGTGTTTATT[A/G]TGGAAGCTCAAGAGG | 26259 |
rs750706575 | snp | C/G | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028122 | TCCTGTGACGCCATG[C/G]CCACTCACTACTACG | 26259 |
rs750732692 | in-del | -/TGT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939511 | ATTAACACCTGGAGG[-/TGT]TGTTCTACTGAATAT | 26259 |
rs750762730 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002432 | GGAGACTGTTAAGGG[C/G]TGCCATGTTGCAGGG | 26259 |
rs750777936 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950138 | ACATAATCTTCCTTC[C/T]CCACCATATAGTACC | 26259 |
rs750778010 | in-del | -/AGAA | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975148 | AAGGATGATGAAAAT[-/AGAA]AGCCACCATTTGGCA | 26259 |
rs750783376 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915745 | GCAACCCTGACTTCC[C/T]GGGTTCAAGTGATTC | 26259 |
rs750784821 | snp | A/G | 9.92621e-05 | 0.00704423 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964800 | CCTGGAATGCAGCCA[A/G]ATGTCTCCTTTGTGA | 26259 |
rs750798210 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959230 | TTAGTGGTCGAATTG[A/T]TGGGTTAGGGTCAGG | 26259 |
rs750834711 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016643 | GTTCTATTTGTCTGG[G/T]TTTTTTTTTTTTTTC | 26259 |
rs750860645 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971820 | TGTTTGAGGCTGTTG[A/G]TACCAAGTGACCACC | 26259 |
rs750882117 | in-del | -/CAGATGTTC | 3.31829e-05 | 0.00407313 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928143 | GTAAGGTGTCACCAA[-/CAGATGTTC]CAGATTTTCCTAAAT | 26259 |
rs750913831 | in-del | -/TGAT | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029005 | TATCAAAGCGAAAAC[-/TGAT]TGATAGAACTACAAA | 26259 |
rs750922761 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116958052 | ATTGACTCTGACTCT[A/T]TTGATTGTGATTAAC | 26259 |
rs750947121 | snp | C/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984849 | TTAAAAATTAGCTGG[C/G]TATGGTGGCACACGC | 26259 |
rs750970417 | in-del | -/C | 1.64757e-05 | 0.00287012 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988748 | TGTACCTGCTCAAAG[-/C]CGAAGACTCCGCCAG | 26259 |
rs750992227 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938984 | GGTTGGGTGGGAAGT[A/T]GATGAGAACTGTGGG | 26259 |
rs750994625 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970364 | CATCAAGCACGGCAA[A/G]GTGGCTTATCCACCT | 26259 |
rs751039521 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937480 | AGGAAGAAAACCCAG[A/G]TGTGTCGTTCCTTGG | 26259 |
rs751048944 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939676 | ATGCCCAGGATCAGA[A/G]TAAAGCTGCCCTGTG | 26259 |
rs751088685 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956477 | TCAAATATGTTTTTA[G/T]TTTTCTGAGCCCCAT | 26259 |
rs751095282 | snp | A/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985065 | GTATATATGAAACGT[A/T]AGTGATTTCGTGTTT | 26259 |
rs751123113 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939086 | TCTCTAAAGTGACTT[C/T]TGCAGAGCACTGGGC | 26259 |
rs751124847 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026045 | TCCTGCCCAGAACTC[A/T]CTGACTTGCTCAAGG | 26259 |
rs751163360 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949641 | AGGTGCCGTGAGCGA[A/G]CTGGAGCATGTTCCT | 26259 |
rs751163842 | snp | C/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909002 | TCTTGGGAGGACAAT[C/T]CTGAGCTGTGTTCTA | 26259 |
rs751196887 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978562 | TTCAGTATCTCTGAA[C/T]GCAGTTAATTGATCC | 26259 |
rs751213188 | snp | A/C | 1.64746e-05 | 0.00287002 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949738 | CCACTGAGTGCTCTG[A/C]ATCTGAAGGTCTTTC | 26259 |
rs751296718 | snp | G/T | 9.90508e-05 | 0.00703673 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988711 | AGGTACCCTGTGGCA[G/T]TAGCCGCTGCTGGAG | 26259 |
rs751320251 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917905 | GCTGAGGCAGAAGAA[C/T]TGCTTGAACCCGGGA | 26259 |
rs751382356 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008124 | TGTCAAAAAAGAACA[A/G]CTGGAAGACATAAAG | 26259 |
rs751382989 | snp | C/T | 1.68821e-05 | 0.0029053 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945344 | AGAATTTGACATTTG[C/T]GTCACTTCTGCTGTT | 26259 |
rs751398793 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965032 | GCCAACAACCGTCAA[G/T]GCATTAGTAGGCATT | 26259 |
rs751404851 | snp | A/T | | | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977960 | ATATTCAATCTTACT[A/T]CCTCTTCTCTTGACT | 26259 |
rs751418793 | snp | C/T | | | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024194 | TCGCCCTGTCGCTCT[C/T]CGCCCATCAGCTCAG | 26259 |
rs751434360 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963238 | GCAATATATGTATTT[A/G]CTGTAGATTAAGAAT | 26259 |
rs751465679 | snp | C/T | 3.41875e-05 | 0.00413431 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027359 | TGCAGGCCCAGTGGA[C/T]GCCCCCTTACGAGCT | 26259 |
rs751561361 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116931215 | AGGCTTATTTCTGGG[C/G]TCTCAGTTCTGTTTT | 26259 |
rs751565865 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990331 | TCTCCGTTGTGTCCT[A/G]GCTGGAAGATGTGTC | 26259 |
rs751583937 | snp | C/G/T | 3.46076e-05 | 0.00415967 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985433 | TGGTCATCTTATTTT[C/G/T]TATTCTTAGAATCTC | 26259 |
rs751585407 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000242 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 26259 |
rs751605874 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012135 | GGCTGACTGTATACA[C/G]TCAGTAAAGCTGACT | 26259 |
rs751621238 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955414 | GTTCATAAGTCACCA[A/G]TCTCTACAGAATCAG | 26259 |
rs751633706 | snp | A/G | 6.60764e-05 | 0.00574751 | synonymous-codon, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024150 | GGGCCTGTCCAGGGT[A/G]AGGATCCACGACCTC | 26259 |
rs751663253 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947152 | ACCTAGCATTTGGCA[C/T]TTAGTAACACTTTAC | 26259 |
rs751670633 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998915 | ACACATCGCAGCTTA[C/G]ACTCACAAAATATTA | 26259 |
rs751693460 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116911817 | TAGGAAGTAATTTTA[C/T]CTTTGTATACTGTTT | 26259 |
rs751737774 | snp | C/T | 5.04851e-05 | 0.00502394 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028214 | GAAAAATGGGAAGAA[C/T]CAGTTTTATCCATCT | 26259 |
rs751741110 | in-del | -/C | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031244 | CCCCTTGAAATCTTA[-/C]CTCCCACCGTGGTGG | 26259 |
rs751761724 | snp | A/C | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945435 | CCAGCAGGAAGGGCA[A/C]CTTCCGGATAGCAGC | 26259 |
rs751773929 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936411 | CCTTTCATGATAAAA[A/C]GCCCTTTGCCGATGT | 26259 |
rs751843219 | in-del | -/CCTTA | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910552 | ATCAATCCTTACTCC[-/CCTTA]CCTTACCTTACCTTA | 26259 |
rs751859091 | snp | G/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981492 | CAAAAGTAATAACAA[G/T]GTATTTAAGGTTTAC | 26259 |
rs751868143 | in-del | -/T | 2.18615e-05 | 0.0033061 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988918 | AAGAATATAGATTTA[-/T]TTTTTAGAAGGGAAT | 26259 |
rs751909849 | in-del | -/ATCA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116997851 | ATGGAATCTCATTCT[-/ATCA]ATCACCCAGGCCAGA | 26259 |
rs751940058 | snp | A/G | | | intron-variant, missense, synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116918698 | AAATTGTTCAGACTC[A/G]AATCCATTGCCCATT | 26259 |
rs751947335 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116948222 | TAGTGTTTGCATAAA[C/T]GCAGGTTTTCATCTT | 26259 |
rs751949631 | snp | A/G | 1.69738e-05 | 0.00291317 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964858 | CTTATGAGGATGGTA[A/G]GTAACCACAACCCTC | 26259 |
rs751950694 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116993604 | GTTTTGGCTTTTTTT[C/T]CTGCTGATTTATTTG | 26259 |
rs751981642 | snp | C/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909242 | TGAGCCCTGGGTTTG[C/T]AGGCAGCTAGTTTAT | 26259 |
rs751982412 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960736 | ACTATTTATGATGAG[C/T]TCTGCATAAGGCACT | 26259 |
rs751993190 | snp | C/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917334 | TCCCAAGAATCCTTG[C/G]TTGATCCATGGGTGG | 26259 |
rs751994336 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004956 | CTTATTAAACAGAAT[A/G]TCTGAAGGACTGTTT | 26259 |
rs752063121 | in-del | -/GAA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016625 | GTTTTCAATTTTGAT[-/GAA]GTTCTATTTGTCTGG | 26259 |
rs752117734 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959580 | GAAGCAAAATGGAAA[C/T]GCTGCTGGATACTTA | 26259 |
rs752122530 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973269 | GATTAGAAAATTACA[C/T]ATTGGCAACCATCAC | 26259 |
rs752136364 | snp | G/T | 1.70206e-05 | 0.00291719 | synonymous-codon, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985207 | TTCTTGCTGCATAGG[G/T]TTTCTTAATATTTGG | 26259 |
rs752146856 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960792 | AGGGCCTTCTTGAAG[A/T]CTTTACAGTCAAGTT | 26259 |
rs752151614 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003358 | CCTTCCAGACAGTGC[A/G]GGGGGCGCACCCTGG | 26259 |
rs752158111 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916744 | CTTAAAAACACCATC[C/T]AAAACGTTGGCTTAA | 26259 |
rs752163152 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928581 | AGTCCAAATTACCCT[C/T]TAAACTTTAGGATCT | 26259 |
rs752183037 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917445 | ATAAAATCTGGTACT[A/G]CCTTCTTACACTTCC | 26259 |
rs752208312 | snp | A/T | 1.65143e-05 | 0.00287348 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027453 | CGGCCAACGTGCCTT[A/T]CCAGACGGTAATGCG | 26259 |
rs752224116 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032387 | GTGCCCAGAAAGCTC[C/T]CCGACCGGGAGGACG | 26259 |
rs752235135 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973498 | GTAATGGTAGAATTG[A/G]TAACCTGTGCCATGT | 26259 |
rs752235899 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928644 | AGACCCACCAAGGGA[A/G]TTACAGATCAATGTC | 26259 |
rs752240415 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117005061 | ATGTTGTCAGAGGTG[A/G]GACTGTCGGACTGGA | 26259 |
rs752241555 | snp | A/G | | | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977735 | CGTTACCTGCCCTCT[A/G]GAACTTTCCCTTGTA | 26259 |
rs752242305 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016870 | TCCAGCTATCCTGGC[A/G]CCATCTGTTGAAAAG | 26259 |
rs752287359 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929258 | TTCTTTTTTTGAGAC[A/T]GAGTCTTGCTCTGTC | 26259 |
rs752294532 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975666 | TAGTTAACATGGCCA[A/G]TAATGAAACTTTGAT | 26259 |
rs752339795 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941391 | CACTTATTTATGCCA[C/T]GTGATCTAACTTCGG | 26259 |
rs752339865 | snp | A/G | 3.29511e-05 | 0.00405887 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964726 | ATGTGAGAGTGTGGG[A/G]CACCCGCACCTGGGA | 26259 |
rs752344433 | snp | A/C | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986346 | AAAATGTGAAAGTAC[A/C]TTTCTGTTCTCAAAA | 26259 |
rs752410704 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116940305 | CCACAGACCATATTT[G/T]GCAGATGACTTATGG | 26259 |
rs752457585 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027334 | GAACTCCCAGGCCTG[C/T]GGCAGCAAGTGCAGG | 26259 |
rs752514205 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987805 | GACACAATAAAGCTG[A/G]TGGTGGGAAATCTCC | 26259 |
rs752557410 | snp | C/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909203 | GAAGGTTGTCCAAGC[C/G]TGGTTTCCCACAGTA | 26259 |
rs752616383 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988782 | CCTCCTTTACGCCCA[C/T]GGCCCGCCTGTCACA | 26259 |
rs752634608 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964533 | CTTCTGTCATCTAGT[G/T]GACATTTTCTCCTGT | 26259 |
rs752647598 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965770 | ACATACATACCTATA[C/T]ATATTTGAGACAGGG | 26259 |
rs752715500 | in-del | -/GT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921528 | TGTATTTCATTTTAC[-/GT]GACAATGACTTACCT | 26259 |
rs752716219 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989572 | TTTTTAATGGAAATT[C/T]TTTGAGTGATGACTA | 26259 |
rs752723013 | snp | G/T | 0.000313095 | 0.012508 | missense, synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945442 | GAAGGGCACCTTCCG[G/T]ATAGCAGCATCTCTG | 26259 |
rs752772480 | snp | G/T | 1.67399e-05 | 0.00289304 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985218 | TAGGGTTTCTTAATA[G/T]TTGGGATTTAAGGAC | 26259 |
rs752788686 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001084 | AATGGAAGGATATTC[C/T]GAAGGAATTTGTGTG | 26259 |
rs752803850 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030066 | CCAGAGAAAACCGAG[C/T]CCTCTCAGTTGCACA | 26259 |
rs752812167 | snp | A/G | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024160 | AGGGTGAGGATCCAC[A/G]ACCTCCGCAGTGGTA | 26259 |
rs752850577 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116914137 | ATTTAGCTAGGTGTG[A/G]TGGTGCACCCCTTTA | 26259 |
rs752853549 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970180 | CGCTCCCTGGTCACC[A/G]AGTTTGTCTTGAAAT | 26259 |
rs752891808 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029065 | AAATCAGTGAGAAAA[A/G]TGTAAAGATCTGGAG | 26259 |
rs752903649 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926413 | GACCACGATTGCAAA[C/T]GAAAGTTTCTTCGTG | 26259 |
rs752923248 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956593 | AAAATTGGTGTCTGA[A/G]TCTTTGGTTGGTTCA | 26259 |
rs752941151 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116967869 | TCTCCTGGGGTCAGG[C/T]GATTCTCCTGCCTCA | 26259 |
rs752968766 | snp | A/G | 1.79178e-05 | 0.00299309 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964893 | CTATTAAGGAAAAAA[A/G]AAAGCTTTACAAAAA | 26259 |
rs752984239 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932666 | TCAGCCTCCCAAGTA[C/G]CTGGGACTACAGGTG | 26259 |
rs752996541 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994328 | AAGTATGGTACTGGT[A/G]TAAAAGTAAATACAT | 26259 |
rs753013450 | snp | C/T | 3.29549e-05 | 0.00405911 | stop-gained, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024202 | TCGCTCTCCGCCCAT[C/T]AGCTCAGGGTCTCTG | 26259 |
rs753023439 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969018 | CTGCCTTTATAAGCT[C/T]TTAGCTATGAAATTC | 26259 |
rs753038101 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012442 | TTAGGGGCCAGCCAT[C/T]ATATGTAAGAATACT | 26259 |
rs753043427 | in-del | -/AATT | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977245 | CTTTCCTTGAAAGGG[-/AATT]AATTGATAGTATAAT | 26259 |
rs753044864 | snp | A/C | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982736 | GAAAAATGATGCCAG[A/C]AAAGCCAATACTTGA | 26259 |
rs753058127 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966099 | ATATAATTACTTTAG[-/C]AACGTGATGTTGGTT | 26259 |
rs753082491 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024731 | CACCCCACCTGCCCA[C/T]AGGTGGAAGGCAGGG | 26259 |
rs753094701 | snp | A/C | | | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949632 | GAATCGCAAAGGTGC[A/C]GTGAGCGAGCTGGAG | 26259 |
rs753106099 | snp | C/T | 8.26276e-05 | 0.00642705 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010273 | GAAAGTATTTGATGT[C/T]GGCCTGGTGTGTGGA | 26259 |
rs753116676 | snp | C/G/T | 8.24143e-05 | 0.00641881 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028109 | TGTCTGCCGTTCATC[C/G/T]TGTGACGCCATGGCC | 26259 |
rs753138044 | in-del | -/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930602 | TTATAGGTTGTCTCT[-/G]TATTCTGTTGATTGT | 26259 |
rs753138818 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995130 | GTGAATGACTAGAAC[A/G]CATGACTTCATCTAG | 26259 |
rs753298263 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116993985 | TTTATTGAATTGGGT[G/T]TCCCGTCCTCAGTGT | 26259 |
rs753304747 | snp | G/T | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028058 | CCGCGCCTATGAGTT[G/T]GCGGTGGACCAGCTG | 26259 |
rs753325159 | snp | A/G/T | 1.64732e-05 | 0.0028699 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949715 | TTGCGGGGTAAGCCA[A/G/T]ACCGTTTCCACTGAG | 26259 |
rs753337987 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962842 | GCAAATGGCCTGAGT[C/T]GTTCTCAGGGTGTCA | 26259 |
rs753387311 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995205 | GTGGCAAGAAAGATC[A/G]GCAGCGTACGCGGAC | 26259 |
rs753420812 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116961336 | TTCCAGGCAAATTTA[A/G]TGTGCAGCCCAGGCT | 26259 |
rs753422342 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919695 | ATCTATGTTTGTTGA[A/G]TTGAAATAATGTGGG | 26259 |
rs753475496 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116918989 | TCCTATATACACAGA[A/G]CAATGATAAAGTTTA | 26259 |
rs753475908 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930874 | ATGCAGTGGTACAAT[C/T]GTAGCTCACTGTAGC | 26259 |
rs753485447 | in-del | -/CAT | 3.29728e-05 | 0.00406021 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010468 | CGTGAGTTGGAAGGG[-/CAT]CATTGCCTTGCAGCC | 26259 |
rs753486680 | snp | A/G | 1.83498e-05 | 0.00302895 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027521 | TTAGTGGTGGGGCCG[A/G]GCGAGTAAGAGACCA | 26259 |
rs753488665 | in-del | -/GA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996737 | GTTTTCTGGGCTGTT[-/GA]GTGATGCTGACTCCC | 26259 |
rs753491138 | snp | A/C | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975289 | GGGTGACTTATAAAC[A/C]ACAGAAGTATATTTC | 26259 |
rs753495098 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943368 | TTGCTGTTATTGCTA[C/T]TGTTATTTTTGTTGT | 26259 |
rs753504213 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020917 | TGTCTGAAACAGAAG[-/C]CTCTTTTGCAACTAA | 26259 |
rs753539482 | snp | C/G | 0.00011533 | 0.00759287 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988720 | GTGGCAGTAGCCGCT[C/G]CTGGAGATCTGATGT | 26259 |
rs753583688 | snp | A/C/G | 8.23803e-05 | 0.00641749 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024220 | CTCAGGGTCTCTGCT[A/C/G]TGCAGATGGATGACT | 26259 |
rs753600828 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973740 | CCTGACAATGGAGTG[C/G]AGTGTGTCATCCTGG | 26259 |
rs753605560 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028633 | TCCATGTCCTTTTCC[C/G]TGTATTTACTTGGGG | 26259 |
rs753641736 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941734 | TGACTTATGTCTTTT[G/T]TATACCTCTGTCCCT | 26259 |
rs753687528 | snp | A/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986671 | AAAACGAATACTGTA[A/G]ACCAGCAATCACTGT | 26259 |
rs753708747 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116911496 | AACACCAATGTTTGT[C/G]CTTGCATAGGGGTCT | 26259 |
rs753725538 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953230 | TCTCAGTTTAGAATC[A/G]TACATTTTTAAACCT | 26259 |
rs753751353 | snp | C/T | 3.45155e-05 | 0.0041541 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945571 | TGAAAGAATAGCCTG[C/T]AAGGACATGGGAATC | 26259 |
rs753753872 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950370 | TGAACTACAGCCTCA[G/T]ACTGTATACTTAATG | 26259 |
rs753804526 | snp | C/T | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949621 | TTCCTCACGCAGAAT[C/T]GCAAAGGTGCCGTGA | 26259 |
rs753837376 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116967601 | ATTACATGTGGACAT[A/C]TTTTCTTTGTGTGTT | 26259 |
rs753858787 | in-del | -/C | 1.67784e-05 | 0.00289636 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928014 | CTTTCTTTTTTTTTT[-/C]CCCCTCAGAATGAAA | 26259 |
rs753901060 | snp | C/G/T | 3.32161e-05 | 0.00407519 | stop-gained, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928067 | TATCCAACTGCCTTA[C/G/T]GAATTGGCAATCAAT | 26259 |
rs753922188 | in-del | -/ATTTA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008661 | TTCAAGGTAGAGAAT[-/ATTTA]ATTTATTATTAACTT | 26259 |
rs753928400 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030866 | AAATGCTCCTTTATA[A/G]GCCAACATGTATCCA | 26259 |
rs753963294 | in-del | -/A | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909304 | AGACTAAGAAGAGTT[-/A]AGACAAGGAATAAGG | 26259 |
rs753965292 | snp | A/C/G | 0.000230728 | 0.0107384 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028061 | CGCCTATGAGTTTGC[A/C/G]GTGGACCAGCTGGCC | 26259 |
rs754013997 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994023 | AAAACAATCCTAAAA[G/T]TAATATGGAACCAAA | 26259 |
rs754021699 | in-del | -/TAATC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968137 | ACAATGTTAATTTTT[-/TAATC]TAAAAGTGAGTGGGG | 26259 |
rs754026942 | in-del | -/AA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954113 | GGCGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 26259 |
rs754036255 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020780 | AAGTCGCAGCTCACC[C/T]TCTCCTGTCTGGTTT | 26259 |
rs754043307 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946013 | ACATTTATCACTTCA[A/G]AGTCTCTACGGAAAT | 26259 |
rs754045446 | snp | C/T | 1.64841e-05 | 0.00287085 | stop-gained, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024295 | GATTATCGGATGAAC[C/T]AGAAGCTGTGGGAGG | 26259 |
rs754096413 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116957860 | TCTGGTAAATAAGTC[G/T]GAGGTAAGATATTGA | 26259 |
rs754118294 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930240 | TTTTAATATTCTAAG[A/G]AACCTGTTTCCTTAA | 26259 |
rs754178024 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953675 | CTACTCAGGAGGCTG[A/C]GGCAGGAGAATGGCG | 26259 |
rs754197654 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970295 | ACGCGATCTGGTGCA[C/T]ATTAGCATGAGGAAG | 26259 |
rs754232883 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116952498 | TTCTTTAAGGCCTAC[A/T]CCAGTCCTGTCTCCT | 26259 |
rs754246381 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117024871 | GGGTTCAGGCTCCAA[C/T]GAAGGAGGAATTTGT | 26259 |
rs754254779 | snp | A/C | 1.6476e-05 | 0.00287014 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949744 | AGTGCTCTGCATCTG[A/C]AGGTCTTTCATTTTT | 26259 |
rs754283786 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983689 | GTCTGTTCTAGATAA[C/T]AGGAAGTTATAGGAA | 26259 |
rs754290058 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937486 | AAAACCCAGATGTGT[C/T]GTTCCTTGGGACCAT | 26259 |
rs754315149 | in-del | -/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975486 | TGGTACCATCACTTA[-/G]GGGGTTAGGATTTTA | 26259 |
rs754348610 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996059 | GTTGATGACGAGCCC[C/T]AGGCCTCATAAAGGA | 26259 |
rs754367178 | snp | G/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985477 | AGCACGTACTAATGG[G/T]GTTGGTAACTCCCAT | 26259 |
rs754393556 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959642 | TATTTATTCCTTCTT[A/C]TTCTTCTAGTCCCTT | 26259 |
rs754412833 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950617 | TTAATATTTTGTGGC[A/G]TGCAGTGCCTATGAA | 26259 |
rs754445219 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010354 | TGGAAGCAGGACGCC[A/G]CCTCTTGAAGCTGGG | 26259 |
rs754447206 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982944 | CAGCTAAATTCCAGC[C/T]CAACTTCATGACGTA | 26259 |
rs754493800 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939695 | AGCTGCCCTGTGTTT[A/C]CTGAGCACGTTCTGC | 26259 |
rs754494990 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117006393 | GAAGAAGTTGGTCTG[C/T]CTTGAGCTCACCCCG | 26259 |
rs754495862 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016764 | GTTTTATAGTTTTGG[C/T]TCTTACACTGAGGTC | 26259 |
rs754524811 | in-del | -/A/AT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933030 | TCACTTAAAAAAAAT[-/A/AT]GTGCTGAAGTGTAAA | 26259 |
rs754543827 | snp | A/C | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985348 | TGTCGTGATGTTATC[A/C]CCCAATGAGGAGGGG | 26259 |
rs754561968 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927269 | CTCTCAAATAAAGCC[C/T]GTTACCTCATCTCTA | 26259 |
rs754570735 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985074 | AAACGTAAGTGATTT[C/T]GTGTTTAGACTTGGG | 26259 |
rs754639619 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116949739 | CACTGAGTGCTCTGC[A/G]TCTGAAGGTCTTTCA | 26259 |
rs754656208 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117015107 | CCCTTTTGTTCCTCT[A/G]GTCAGAAAGATGGAG | 26259 |
rs754689038 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939102 | TGCAGAGCACTGGGC[A/T]TTTGAGATACTCGTT | 26259 |
rs754693708 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025298 | GTGACTGTGTCACTG[C/T]ACTCCAGCCTGGGTG | 26259 |
rs754720956 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020965 | GCGTGTATGTGGACT[C/T]TTGTGTAGCTACCTC | 26259 |
rs754759978 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951630 | TTTGCATTTACACCT[A/G]TTAAGTACATTTCAC | 26259 |
rs754766971 | in-del | -/TAGAG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016486 | ATATTATTGAGTTAT[-/TAGAG]TATTTTTTTAATATA | 26259 |
rs754779811 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996386 | TCATCACGAGTTGAA[A/G]TATCTGTCTGGGAGA | 26259 |
rs754824526 | snp | C/T | | | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978227 | TCCGTGGTTTAGCTG[C/T]TCTTTATGACCCTTG | 26259 |
rs754845865 | snp | C/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945439 | CAGGAAGGGCACCTT[C/G]CGGATAGCAGCATCT | 26259 |
rs754917197 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963460 | AAAAAACAAACTAGC[C/T]GGACATGGTGGTGCA | 26259 |
rs754941569 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983420 | CTGTGTTTTAGATGC[A/G]AAGCAACATTTAGCT | 26259 |
rs754961665 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920261 | AATGATGCCTGTGTA[C/T]ACTAGAACAACTTGT | 26259 |
rs754977736 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020724 | GTTTGATGAAACCAC[A/G]GAGCTGAGCCTGGCG | 26259 |
rs754981413 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924055 | CCATGTTGATATTTT[A/T]ATAGTTTGACCAGAT | 26259 |
rs754982826 | snp | A/C | 1.65081e-05 | 0.00287293 | synonymous-codon, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024156 | GTCCAGGGTGAGGAT[A/C]CACGACCTCCGCAGT | 26259 |
rs754990827 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956443 | TGGCTGCTGCTTCAG[C/T]TGCCAGACATGGCCT | 26259 |
rs755028773 | snp | A/T | 1.67337e-05 | 0.00289251 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945356 | TTGTGTCACTTCTGC[A/T]GTTTTAGGTGAGCAA | 26259 |
rs755056483 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116911853 | ATTTAATTTTTGTAA[C/G]CGTGCACGTATTCAA | 26259 |
rs755113545 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955451 | GTCTTTCTCTCAAAG[C/T]TCAGCGCCTGTCTGC | 26259 |
rs755136401 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994137 | AGGCTATAGTAATAA[A/T]AACAGCATGGTACTG | 26259 |
rs755177728 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116967924 | GGCGCCTGCCACCAC[A/G]CCCAGCTAATTTTTT | 26259 |
rs755178992 | snp | G/T | 1.64833e-05 | 0.00287078 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010460 | CGGGAGGTACGTGAG[G/T]TGGAAGGGCATTGCC | 26259 |
rs755183425 | in-del | -/ATAT | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909733 | TCTAGAAGGGAAGGG[-/ATAT]ATATATATACATAAA | 26259 |
rs755207406 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930387 | TTTGCATTTCTCTGA[C/T]GATTAGTATTGTTGA | 26259 |
rs755229147 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965471 | TATAACTACTAGAAA[C/T]GGTCATTTCAATGGC | 26259 |
rs755236487 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027533 | CCGGGCGAGTAAGAG[A/G]CCATCTTAGTTTGAC | 26259 |
rs755264101 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992169 | AAAGCTTATCTGTCT[A/G]ATCTTTTTTTTAAAA | 26259 |
rs755287769 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116958558 | GAATACCACACACAA[-/C]CCCCCTGGTCATGGC | 26259 |
rs755328748 | snp | A/G | 4.94287e-05 | 0.00497111 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988807 | GTCACATGTCTAGAC[A/G]TCTCGGCCAACCAAG | 26259 |
rs755377064 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023000 | TTCTGGTATTTTGCT[A/G]TGCCACTTTCTTTCA | 26259 |
rs755404336 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947320 | GGAGACTTCTATTTG[A/G]AGCGTGTAAGGTCCA | 26259 |
rs755435670 | snp | G/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980093 | GACTCAAACTTTGTT[G/T]CATTCTTGGAGTAGA | 26259 |
rs755468977 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022108 | GCCCTGGAGGCAGCT[C/G]GTCCTTAACAGGTCT | 26259 |
rs755473285 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960765 | CTGTGATGGAGGCTA[C/T]GGCACTGCGGTAGGG | 26259 |
rs755481322 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031304 | CCCAGAACCTCCCCT[A/C]CAGGCGCTCCCAGCC | 26259 |
rs755485360 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917356 | CATGGGTGGCTCCTG[A/G]AAGGAAGAGTTAGTT | 26259 |
rs755492051 | snp | C/T | 0.00904959 | 0.0666551 | intron-variant, synonymous-codon, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116911166 | GCCGGAGGTGGGCTC[C/T]GGGCGCGGCGAACAG | 26259 |
rs755500795 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032342 | AACAAACCTCACCTG[C/T]ACATCTTTGGGGCGT | 26259 |
rs755502394 | snp | A/G | 1.65389e-05 | 0.00287562 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027473 | ACGGTAATGCGAAAC[A/G]CCGACCTGGACAGCT | 26259 |
rs755521044 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116948376 | TGTAGGACAGCTCCA[C/T]GTGGATGTGTCTAGT | 26259 |
rs755523188 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020648 | ACTATACTTTCATGC[-/T]TTTGTATTGAAAGCA | 26259 |
rs755564545 | snp | A/G | 3.30256e-05 | 0.00406346 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027457 | CAACGTGCCTTACCA[A/G]ACGGTAATGCGAAAC | 26259 |
rs755595921 | snp | C/T | 1.65488e-05 | 0.00287647 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988620 | TATTTTTGATCAAGT[C/T]AGGATGAATTTATGG | 26259 |
rs755607576 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116961631 | AGTCTGTCTGTTCCA[A/G]TCATTGCATGCACAG | 26259 |
rs755615235 | snp | A/G/T | 3.29529e-05 | 0.00405901 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988717 | CCTGTGGCAGTAGCC[A/G/T]CTGCTGGAGATCTGA | 26259 |
rs755626065 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960891 | TGAGTCAGAAAGCTT[C/G]AGGCTTCAAGGAGGG | 26259 |
rs755683763 | snp | A/G | 1.65891e-05 | 0.00287998 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945371 | TGTTTTAGGTGAGCA[A/G]GACGTGGAAGGTGAT | 26259 |
rs755693780 | snp | C/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917509 | CTTTCATTAGTGCAC[C/G]CTGTTGTATTTCTGG | 26259 |
rs755710991 | in-del | -/GATGGTGT | 1.64731e-05 | 0.00286989 | frameshift-variant, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949686 | GATGTGCATTCTCAC[-/GATGGTGT]GATGGTGTGGTCATT | 26259 |
rs755715976 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973574 | ATTCCAGCCAAAAGT[A/G]CACAGCCTGATCTAA | 26259 |
rs755729644 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929295 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTTCC | 26259 |
rs755734014 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992602 | CAATACCACTCTGTG[C/T]CTCTGCATACCCATA | 26259 |
rs755740375 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959768 | AGCTTGAGAGAGGCT[C/G]TATTCCCATTCTTTC | 26259 |
rs755788044 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003976 | TTTCAGTTGTAGAGA[A/G]TTCTTGGCCCTTATC | 26259 |
rs755802789 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983009 | GTTGTTTAACCGCTC[A/G]GTGCTTCTGTTTCTT | 26259 |
rs755857087 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928722 | TGGGAGATATCATTT[A/G]GGCCAAACTGCATTG | 26259 |
rs755880098 | snp | C/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910482 | CAGTTTCTTTATCCA[C/T]CTGTTGATTCTCTTT | 26259 |
rs755906161 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116940022 | CAGCATTGCTGAGTC[A/G]TTATCCCGTTCTTTA | 26259 |
rs755907215 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968249 | GAAATCTTGCTGCCA[-/C]CCACTTTTGTCTGCT | 26259 |
rs755956672 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016895 | AAAAGACAATTCTCT[-/C]CCCCCATTCAATTGT | 26259 |
rs755978794 | snp | C/T | 4.9476e-05 | 0.00497348 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024163 | GTGAGGATCCACGAC[C/T]TCCGCAGTGGTAACA | 26259 |
rs756004478 | snp | C/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909221 | GTTTCCCACAGTAAG[C/G]AAGCCTGAGCCCTGG | 26259 |
rs756029722 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921772 | ATAAAAGTCTTTAGT[A/G]ATATAATTGCTTAGA | 26259 |
rs756032896 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939238 | AACTTTTTCAGTGCT[C/T]ATTGGAGCATTTTGG | 26259 |
rs756048137 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951826 | AGTGAAATCTGAAAA[C/T]AGTCACTCGTTGATA | 26259 |
rs756060017 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922704 | ATGGATCTCTTTGCA[A/G]TTTCTCTCAGTGTTT | 26259 |
rs756068565 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979599 | CTTTTCCTGTTTGTT[A/G]TGAGTGAAACAGTAT | 26259 |
rs756084312 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962221 | GGCTTGCCCAGGAGC[A/C]CCTCAGATATGAATA | 26259 |
rs756116959 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116931270 | GCCAGTGACATGCTG[C/T]GTACATTGCTATAGC | 26259 |
rs756123296 | snp | C/T | 4.0012e-05 | 0.00447263 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911005 | GGCACCCGGTGGAAC[C/T]GAGGAGAACGTGGAG | 26259 |
rs756135708 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944007 | CTGGGGATTTGATTT[G/T]TGGGGACCTCTAAAC | 26259 |
rs756191522 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977007 | CAGGGGAGGGAGACC[C/T]GAGAGCCCCACCCCA | 26259 |
rs756208525 | snp | G/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975649 | CCTTAACCAAGTGAT[G/T]ATAGTTAACATGGCC | 26259 |
rs756239272 | snp | A/G | 0.000381448 | 0.013805 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928116 | AGGAAAGAACTAGGA[A/G]GATGTGCACAGGTAA | 26259 |
rs756241974 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944141 | GAATTAGCACACATT[A/G]AAACAACTTAGACGT | 26259 |
rs756275526 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989840 | TAACCCTCTTTATGC[C/T]TCAGTTTCCTCATTT | 26259 |
rs756278002 | snp | G/T | 1.64768e-05 | 0.00287021 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024206 | TCTCCGCCCATCAGC[G/T]CAGGGTCTCTGCTGT | 26259 |
rs756299709 | snp | G/T | 1.69833e-05 | 0.00291399 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027985 | CTGGGGTGAGGGCCA[G/T]CGAGGCAGCCCTGAC | 26259 |
rs756305382 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030089 | GTTGCACACGTGTAC[C/G]TATCAGTGGGAAGTG | 26259 |
rs756321774 | in-del | -/CA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954111 | AGGGCGACTCTGTCT[-/CA]AAAAAAAAAAAAAAA | 26259 |
rs756350014 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013551 | CATTCCACTCACCAC[A/T]CTCTCTCTGGTACTC | 26259 |
rs756351897 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000445 | GCACAGGGGTTCTCA[C/T]ATGCCAGCATGCATC | 26259 |
rs756360140 | in-del | -/TG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921697 | TTGCTTTTCTGTGTC[-/TG]TGAAAATATCATGTG | 26259 |
rs756367050 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116914167 | AGTTCTAGCTACTTG[C/G]GAGGCTGAGGTGGGA | 26259 |
rs756391514 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013894 | AAGTCTGCAGGAAGT[A/G]ATCACTTGTTTTTTT | 26259 |
rs756393522 | snp | A/G | 6.98202e-05 | 0.00590807 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988896 | GCAAGATATATAATT[A/G]ACAAAAAAGAATATA | 26259 |
rs756412844 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969025 | TATAAGCTTTTAGCT[A/G]TGAAATTCACTTTGT | 26259 |
rs756441451 | in-del | -/AATTATTTC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023567 | TATTATAAGGCAAGT[-/AATTATTTC]AATAAGTGACTGCCC | 26259 |
rs756509612 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012443 | TAGGGGCCAGCCATC[A/G]TATGTAAGAATACTC | 26259 |
rs756540210 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950392 | TACTTAATGCCATAA[A/G]GTAGAAAGCAGAACA | 26259 |
rs756544912 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925527 | TTCCGTTAGTGTATT[C/G]GTTTCTTTTTTTTCC | 26259 |
rs756569762 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116967890 | TCCTGCCTCAGCCTC[C/T]TGAGTAGCTGGGATT | 26259 |
rs756588100 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960635 | GGGTGTTTCACTCAT[-/C]ATTACCATTGGAAAG | 26259 |
rs756591982 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924432 | TGTGTTGTAAACATT[A/C]AAAATCTGTTCTTCT | 26259 |
rs756595239 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116972424 | TGAACCCTAGGGCTT[C/G]ATCAAACTAGAAGTA | 26259 |
rs756608976 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935853 | CAGGAGCTGAGCTGT[C/G]TCTATGACCTTTGAG | 26259 |
rs756614314 | snp | G/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982794 | AAACTCCATGTGTGC[G/T]TAGAGTGAGCTGTGG | 26259 |
rs756632523 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981762 | GGGATTACAGGTGCC[C/T]ACCACAATGACTGGC | 26259 |
rs756632639 | in-del | -/TCT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003853 | TGACTGCTTTTAAGA[-/TCT]TCTCCTTGTCTTTAA | 26259 |
rs756646324 | snp | A/G | 0.000148249 | 0.00860829 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949633 | AATCGCAAAGGTGCC[A/G]TGAGCGAGCTGGAGC | 26259 |
rs756687387 | snp | A/G | 4.94271e-05 | 0.00497102 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988797 | CGGCCCGCCTGTCAC[A/G]TGTCTAGACGTCTCG | 26259 |
rs756689499 | snp | C/G | 6.5925e-05 | 0.00574092 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945464 | GCATCTCTGACTATT[C/G]TTGCTGGAAGCTCAT | 26259 |
rs756693234 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950619 | AATATTTTGTGGCAT[A/G]CAGTGCCTATGAAAA | 26259 |
rs756700127 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116910990 | GCGGGACTGTCTCGT[A/G]GCACCCGGTGGAACC | 26259 |
rs756723454 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994034 | AAAATTAATATGGAA[C/T]CAAAAAGAGCCCAAA | 26259 |
rs756828940 | in-del | -/TTG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019843 | TCTTCTCCAAGGTAA[-/TTG]TTGTTAATGTTTCAA | 26259 |
rs756832050 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117006633 | TGGCTAGAAGATGAT[C/T]GGTGGGTCTCCTCAG | 26259 |
rs756865515 | in-del | -/TC | 1.64768e-05 | 0.00287021 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024212 | CCCATCAGCTCAGGG[-/TC]TCTGCTGTGCAGATG | 26259 |
rs756871066 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994171 | GTAAAAGTAGATATG[A/T]ATTGGTACTGGTGTA | 26259 |
rs756891269 | snp | C/G | 1.64762e-05 | 0.00287016 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988721 | TGGCAGTAGCCGCTG[C/G]TGGAGATCTGATGTA | 26259 |
rs756891844 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116961728 | ATCACAGACATGCAC[C/T]ACTGCCATGACGGAG | 26259 |
rs756898469 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116931081 | TAGTGTGAGATGGGA[A/T]CTAATTTCATTCTTC | 26259 |
rs756914337 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982906 | ATGCACTTACAAATG[C/T]AGCCGCTCATCCTGC | 26259 |
rs756918185 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027523 | AGTGGTGGGGCCGGG[A/C]GAGTAAGAGACCATC | 26259 |
rs756931976 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955574 | TTAGTTGATAGTAAG[-/T]GCTCAGGAAACATGT | 26259 |
rs756984352 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919037 | GAGATTAACAGCAAC[A/T]ACAAAATAGAACAAT | 26259 |
rs757053123 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941742 | GTCTTTTTTATACCT[C/T]TGTCCCTTCATCACT | 26259 |
rs757066570 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973774 | GGGTTGTTTTTCTAC[A/G]AAGAACATTACTGGG | 26259 |
rs757079409 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017899 | CCAATTACAGAGTCT[C/T]AGTGCTTGCTTCTTG | 26259 |
rs757106982 | snp | C/T | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985253 | AAGTACCCTGTTCAT[C/T]GTTTTGAGCACGATG | 26259 |
rs757167572 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928831 | TTTCTTTTTTTTTGA[A/G]ATGGAGTTTTGCTCT | 26259 |
rs757171192 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017152 | GGAAATACTCATGAC[G/T]TAGTTAATAACTAAA | 26259 |
rs757176827 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955203 | CCTTCTCTGGCCCTC[A/G]TTCTTGTCTTTCTCT | 26259 |
rs757181842 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987959 | ACCTAACTCATCTTG[C/T]ATCCTTGCTTTACCC | 26259 |
rs757253910 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116940194 | CCGTGTCAGCCTGGG[A/G]GGTGGGCTCCAGTGG | 26259 |
rs757259768 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, stop-gained, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024172 | CACGACCTCCGCAGT[A/G]GTAACATCGCCCTGT | 26259 |
rs757288000 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998792 | TGCATGTCCAGACAG[C/T]TGAGACTGATGCTGG | 26259 |
rs757294807 | in-del | -/C | 1.67784e-05 | 0.00289636 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928015 | CTTTCTTTTTTTTTT[-/C]CCCTCAGAATGAAAT | 26259 |
rs757354236 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933892 | GGAATGTCCTGCTGC[A/T]TTATGATTTTATTTT | 26259 |
rs757395787 | snp | A/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978426 | AAAATTTTTGTCAAA[A/G]TGCCTTTTCCTTTGT | 26259 |
rs757400706 | snp | C/G | 6.59098e-05 | 0.00574026 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985326 | TGGCCACAGCTTCTG[C/G]TTTTGATGTCGTGAT | 26259 |
rs757404746 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011263 | GGTGGCGGGCTGCTC[A/G]GAGGCGGGTGTCAGA | 26259 |
rs757414142 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977170 | ACCGACTGCAGTTTC[A/G]CCATCATTTAAATCT | 26259 |
rs757425322 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915528 | AGAACCACCTCCCCT[A/G]CCCTGTGTTCCCTTC | 26259 |
rs757452017 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946120 | CTGTTTGAGGCATGA[C/T]GAGACAGCAGTGTGG | 26259 |
rs757453330 | snp | A/G | 1.65031e-05 | 0.00287251 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010289 | GGCCTGGTGTGTGGA[A/G]TTGTGGGCCCACACA | 26259 |
rs757455216 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008803 | ACAAAATACTACTAT[C/T]AAAACCTTTGGCTGA | 26259 |
rs757467997 | in-del | -/AGGAACCTTAGAGTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117005417 | AGGATCTCTGTCCCC[-/AGGAACCTTAGAGTT]AGGAACCTTAGAGTT | 26259 |
rs757480914 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928004 | ATTATAAACTTCTTT[C/T]TTTTTTTTTTCCCCT | 26259 |
rs757504140 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989904 | AGAGTTGTAGGATTA[A/T]ATGAAAAGCCATATG | 26259 |
rs757513588 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924223 | GAGTTGGGTTAACGT[A/G]GCCCATAACTTTTTG | 26259 |
rs757537784 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020827 | GGAAGTCACTTCCTA[C/T]GTGAGCTCAGCAGTG | 26259 |
rs757585679 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944417 | ATTTTCCTTCTTTCC[A/G]TCTCTGTCTTTGAGT | 26259 |
rs757591707 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029261 | AAGACACTGCACCCT[A/G]TGGGCTATACCCTCA | 26259 |
rs757596672 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029196 | AAAGAACAGCTCAGA[C/T]GCACAAAGATTCACA | 26259 |
rs757616645 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028980 | GCATCCACCTAATAT[-/A]ACCTTCAGAATATCA | 26259 |
rs757628706 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116914386 | TCAGGAGCTCAAAAC[C/T]AACCTGGGCAACGTA | 26259 |
rs757629664 | snp | A/G | 1.6476e-05 | 0.00287014 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949747 | GCTCTGCATCTGAAG[A/G]TCTTTCATTTTTCTC | 26259 |
rs757639772 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116957979 | TGCATTTATCCATCT[C/T]TGGTTCTCCGAGGAA | 26259 |
rs757681466 | snp | C/G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926458 | TGGCAAGCAGTGACT[C/G/T]CCTCCAGTGTTGATT | 26259 |
rs757715899 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012598 | CTTACATTTTTTCCC[C/T]GGAGGTTTAATAGCT | 26259 |
rs757721439 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964728 | GTGAGAGTGTGGGAC[A/G]CCCGCACCTGGGACT | 26259 |
rs757734344 | in-del | -/TG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018865 | CCTTAACAGCCAAAC[-/TG]TAAATTATGGAGTAT | 26259 |
rs757764440 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956844 | ATGGTGACACGTGCC[G/T]GTAATCCCAACTACT | 26259 |
rs757773620 | snp | C/T | 3.29473e-05 | 0.00405864 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010359 | GCAGGACGCCGCCTC[C/T]TGAAGCTGGGTAACG | 26259 |
rs757778848 | in-del | -/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980538 | TTGCCATTTCACAAG[-/T]TTCACAGTGTCAGGA | 26259 |
rs757786678 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937487 | AAACCCAGATGTGTC[A/G]TTCCTTGGGACCATG | 26259 |
rs757789271 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969237 | TTGATTCGTTTCAAG[C/T]TCATTTTGGTATTAA | 26259 |
rs757792525 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995090 | GCCCTTCATTTAAAT[C/T]ATTTTTCAGCTCTCT | 26259 |
rs757840148 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932971 | ATTTTTTGATGCGGA[A/G]TGTGTGTCTTTAGGA | 26259 |
rs757909940 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983866 | TCCTTTCATCTGCCT[C/T]ACAGTCCTATGTAGT | 26259 |
rs757982210 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937641 | CCAGGGTCAGTGGTG[C/T]GTTGGGGGCAAAAGC | 26259 |
rs757988601 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996253 | TGCGTGTGACAAGGA[C/T]GCTTGCTTGGCGCTG | 26259 |
rs758006752 | snp | G/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983010 | TTGTTTAACCGCTCG[G/T]TGCTTCTGTTTCTTT | 26259 |
rs758019779 | snp | C/T | 6.59065e-05 | 0.00574012 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024243 | GGATGACTGGAAGAT[C/T]GTCAGTGGAGGCGAG | 26259 |
rs758023365 | snp | C/T | 1.64991e-05 | 0.00287215 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949568 | ACGATGCTTGGCTTT[C/T]GGGCTGTCCCGAGAG | 26259 |
rs758035146 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950773 | GGTTGATGGTCCAGA[G/T]ACTTGCGATTCTGTC | 26259 |
rs758047345 | snp | C/T | 4.22931e-05 | 0.00459835 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988915 | AAAAAGAATATAGAT[C/T]TATTTTTTAGAAGGG | 26259 |
rs758074627 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995297 | TGACCTGCCTCTTCT[C/T]TTCTGTAAAATGAGG | 26259 |
rs758097781 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004905 | TCTGGGTTTCATGCT[A/G]TCTCCATTTTGGGCT | 26259 |
rs758101585 | snp | C/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975691 | TTTGATATTATGTAC[C/G]TCCTGATACATAATG | 26259 |
rs758113937 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025130 | AACAGGAGACCCTGC[A/G]TTTGAGACAGGTGGG | 26259 |
rs758133267 | snp | A/G | 4.94181e-05 | 0.00497057 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949630 | CAGAATCGCAAAGGT[A/G]CCGTGAGCGAGCTGG | 26259 |
rs758199870 | snp | G/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985335 | CTTCTGCTTTTGATG[G/T]CGTGATGTTATCCCC | 26259 |
rs758249065 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963139 | TCTTTATCCCACATG[C/T]GCACTCTCTGGGTGC | 26259 |
rs758289889 | snp | G/T | 1.67632e-05 | 0.00289505 | splice-donor-variant, intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985404 | AAGTTCCGAAACTGG[G/T]GAGCTTTTTAGTCTG | 26259 |
rs758338712 | snp | G/T | | | intron-variant, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116976897 | TCAAAATCATTTCAG[G/T]GGGTAATCAAAAAAG | 26259 |
rs758352881 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959545 | AAATTTTGTTTTTAG[A/C]AAATAAGAGCTGACA | 26259 |
rs758359366 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975530 | GGTAGGGGGGACACA[A/G]CATTCAGATGAGCAA | 26259 |
rs758374421 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018170 | TAATTGGTGGGCTAC[C/T]GCCGACTCCTATGGT | 26259 |
rs758383181 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116942196 | ATCACATCTGGCTAA[-/T]TTTTTTTTTTTTTGT | 26259 |
rs758389688 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929659 | TGGCTCAGTTGAGGT[A/G]ACTAACATGTATTAC | 26259 |
rs758392607 | snp | G/T | 1.65116e-05 | 0.00287324 | stop-gained, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024315 | GCTGTGGGAGGTGTA[G/T]TCCGGGTAAGGTGCA | 26259 |
rs758410537 | snp | A/G | 6.64927e-05 | 0.00576558 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028185 | TAGGGATGTGCCTCA[A/G]TTGGGAGCAAGGAGA | 26259 |
rs758440098 | snp | A/G | 6.60088e-05 | 0.00574457 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964646 | CATTTTCCCCACCAT[A/G]GCCCTGCTCTTCAAT | 26259 |
rs758448698 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953283 | CGTTCCAAGACCCTC[A/G]TCTTGCTTGAGGTGG | 26259 |
rs758467886 | snp | C/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909337 | CAGTTAATTGCAAGA[C/G]CATCTTTGAGCCTGG | 26259 |
rs758473954 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966180 | CAGCTGAGCTGTTTC[C/T]GTGGTATAATTAATA | 26259 |
rs758517719 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970198 | TTTGTCTTGAAATCT[C/T]GCTCTTTGGTGAGAA | 26259 |
rs758534382 | snp | A/G | 1.64819e-05 | 0.00287066 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010455 | ATGGACGGGAGGTAC[A/G]TGAGTTGGAAGGGCA | 26259 |
rs758557299 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117010933 | GAACAGATTCCACTT[C/T]CTATTTAGCTGATTA | 26259 |
rs758558801 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021911 | TGGACGTGACTGCCT[C/G]GTTTTTCGTTGATTC | 26259 |
rs758563517 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979882 | TTGTTTTACCTTGGC[C/T]TACTGTGCAGGAGAG | 26259 |
rs758606303 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946855 | AAGCAGAGGGTCTAA[C/G]CCTGGTGGGAGGGGC | 26259 |
rs758645328 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022753 | GTAAACTGCCCCTTC[A/G]TTGTTTTAAGTGCTC | 26259 |
rs758658293 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991939 | ACCTCAGCTGCATGA[A/G]CATGGAGTAATAATG | 26259 |
rs758730320 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978634 | GTTTATTGTGGAAGC[C/T]CAAGAGGATGGGAGC | 26259 |
rs758732006 | snp | C/T | 9.91686e-05 | 0.00704092 | stop-gained, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027467 | TACCAGACGGTAATG[C/T]GAAACGCCGACCTGG | 26259 |
rs758750867 | in-del | -/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909088 | CAGAGATGCTCTTTC[-/T]TTTTTTTTGTTTTTT | 26259 |
rs758771854 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947201 | CTGAATGTCTATTTA[G/T]TATTTATTTCTAATG | 26259 |
rs758795761 | in-del | -/AGGTATAGGTATAGGTAT | 3.33131e-05 | 0.00408111 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928175 | CTAAATGTGTGATTA[-/AGGTATAGGTATAGGTAT]AGGTATAGGACTCTC | 26259 |
rs758801742 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915746 | CAACCCTGACTTCCC[A/G]GGTTCAAGTGATTCT | 26259 |
rs758841455 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932687 | ACTACAGGTGCGCCA[C/T]CATGCCCAGCTAATT | 26259 |
rs758846464 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001613 | GTTTTCACTCCGTAA[G/T]ATAGATATTATAACC | 26259 |
rs758877486 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030373 | TGTAGGTAGCAAATG[C/T]AGGATTTTGTTTACT | 26259 |
rs758894873 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959263 | CTGTGTCCTGCAAAC[C/G]TGAGTCATAATATTG | 26259 |
rs758895185 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971886 | TCACACCAAGTGGCG[G/T]CCACAGTGAATTTTT | 26259 |
rs758915610 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964732 | GAGTGTGGGACACCC[A/G]CACCTGGGACTACGT | 26259 |
rs758946340 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116958072 | TTGTGATTAACCAAG[A/G]TGTATGGAAAACAGT | 26259 |
rs758999564 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014999 | CGCCACCATGCAGCA[A/T]GTGACTGGGGACTGT | 26259 |
rs759046438 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023625 | CCCCGCTCTGCTGTG[A/C]TTATCAAGGATAAAG | 26259 |
rs759057690 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912313 | TTCCCTCAGCATCCC[A/G]CGTAGCTGGGACTAC | 26259 |
rs759058535 | snp | C/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910211 | ACTGAACCCAAGTTA[C/T]AGTCTTTTATCCCTC | 26259 |
rs759084163 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941210 | ATTGCCTGGGCCCCA[C/T]TGGCCAGGGATGCAG | 26259 |
rs759114345 | snp | G/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986265 | ACCTCCAGGAGCGTC[G/T]GCACTTTGAGTATAG | 26259 |
rs759125100 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027868 | CGTTGACCGCTAAGC[C/T]GGGGACTGTGAGTAT | 26259 |
rs759140236 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010666 | TTTCTGAAGCACCAC[A/G]GGAAGGTTTTCTTTT | 26259 |
rs759222173 | in-del | -/CAA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954111 | AGGGCGACTCTGTCT[-/CAA]AAAAAAAAAAAAAAA | 26259 |
rs759241928 | snp | A/G | 0.000148262 | 0.00860865 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010425 | AGCCCTCCCAACCTC[A/G]TGGTCAGTGGCAACA | 26259 |
rs759275514 | snp | A/C | 1.64757e-05 | 0.00287012 | stop-gained, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988776 | CAGAACCCTCCTTTA[A/C]GCCCACGGCCCGCCT | 26259 |
rs759311689 | snp | A/G | 1.64789e-05 | 0.0028704 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988714 | TACCCTGTGGCAGTA[A/G]CCGCTGCTGGAGATC | 26259 |
rs759317012 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116934983 | GCTCCATCTCTAACC[A/C]CTGGCAACCACTGAT | 26259 |
rs759366884 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922601 | AAGAGAAGACAGATT[A/G]AATTTCTAACAGTAA | 26259 |
rs759381305 | snp | A/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979327 | CTGGCATGGGTGCCC[A/G]TCCACAGCTGCTGAG | 26259 |
rs759392979 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965696 | ACAAAACTAAAGTAG[C/T]TAATGGGGAATTTTA | 26259 |
rs759416440 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946787 | GGTCCATGTGATGCA[C/T]ACAGGCAGAAAGGTA | 26259 |
rs759423517 | in-del | -/TC | 1.86336e-05 | 0.00305229 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927999 | TAAAAATTATAAACT[-/TC]TTTCTTTTTTTTTTC | 26259 |
rs759424082 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009542 | AATTTGAGGCAAGGA[C/T]TCTGTCCTCAGCACC | 26259 |
rs759438769 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013455 | ATATTTTGTCTCTTC[C/T]CGCTAAGACTAAGAA | 26259 |
rs759452374 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022259 | CTTATTTTCCCAGAA[A/G]GCCATTTACTCATCT | 26259 |
rs759471380 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991485 | TCCCAAATAGTCTCA[C/T]GTGCGAGGCTTGGTG | 26259 |
rs759493440 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951769 | GAACCTCATGATGGA[C/T]CCAGTCATGGTTCTT | 26259 |
rs759522769 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969901 | CTGGCCTCATATTTC[A/T]TCTGCCTTGTTTCCG | 26259 |
rs759539213 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983433 | GCGAAGCAACATTTA[A/G]CTTGAAGAAGGCTCT | 26259 |
rs759548178 | snp | A/C/T | 4.9418e-05 | 0.00497061 | missense, synonymous-codon, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949686 | TGATGTGCATTCTCA[A/C/T]GATGGTGTGGTCATT | 26259 |
rs759556667 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030744 | GGGTTTTGTAAAGGA[G/T]AATTTTTTGGACTCA | 26259 |
rs759602675 | in-del | -/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920490 | GACAAATAATTGTCA[-/G]GTAATAAATAAATGT | 26259 |
rs759664286 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116934656 | TATAAATTCATAGGA[A/C]GTTGCAAAAAATAGT | 26259 |
rs759689096 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024650 | ATTTTAGGATTTCTC[C/T]ATCTTAATAAACAGA | 26259 |
rs759697145 | in-del | -/AC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019104 | GTGTCTGTAAACGTG[-/AC]AGAGAGAGACCTTTG | 26259 |
rs759727436 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937049 | GTGCTTGGGCCAGGA[C/T]GGCACCAGCAGAAGT | 26259 |
rs759751109 | snp | C/T | 9.88484e-05 | 0.00702954 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949613 | TCCCCCTTTTCCTCA[C/T]GCAGAATCGCAAAGG | 26259 |
rs759776837 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117024070 | TGCATAGACCAGCAC[C/T]GTGGAGGGGGAGTTT | 26259 |
rs759785684 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018400 | TCTTGGCATATTCTG[G/T]TGCCCATTTGCTGTG | 26259 |
rs759786588 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995664 | AATTCTTAAATTAAA[C/T]TGGATTCTTAGGTTC | 26259 |
rs759789149 | in-del | -/CTTAAACAT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021225 | CTGATTACCAGCAAA[-/CTTAAACAT]CTTACACATGTTTAA | 26259 |
rs759802980 | snp | A/G | 1.67337e-05 | 0.00289251 | splice-donor-variant | FBXW8 | GRCh38.p7 | 12:116945529 | CGAACCAACTGGAAG[A/G]TGGGCAGTGGCCAAT | 26259 |
rs759874863 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919558 | ATGCTATTTTACTTC[C/T]TCTTTACTGAAGCTT | 26259 |
rs759890998 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018994 | CTCCCCCTTTCCCCA[A/G]TCCTTTTCAAGTTCC | 26259 |
rs759901832 | in-del | -/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983130 | CTATGCAAATGGGAG[-/T]TTTTTTTTCTCTTTA | 26259 |
rs759936532 | in-del | -/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003357 | CCTTCCAGACAGTGC[-/G]GGGGGGCGCACCCTG | 26259 |
rs759949398 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995046 | ACAAGATGAGGCCAG[C/T]GGGGATATACAGAGA | 26259 |
rs759963255 | snp | A/G/T | 4.98453e-05 | 0.00499205 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928054 | TGCCTTTCTTTGATA[A/G/T]CCAACTGCCTTACGA | 26259 |
rs759982690 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028275 | AAACATTTAGGGGAA[G/T]AAAGCAGCCCAGGGT | 26259 |
rs759997417 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116974631 | TCTGTCATCCAATAA[A/T]AATGAAGCATGGCTG | 26259 |
rs760001832 | snp | C/T | 1.69109e-05 | 0.00290778 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985211 | TGCTGCATAGGGTTT[C/T]TTAATATTTGGGATT | 26259 |
rs760015810 | snp | C/G | 1.64803e-05 | 0.00287052 | missense, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024280 | CTGGTGTCCGTGTGG[C/G]ATTATCGGATGAACC | 26259 |
rs760104424 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929207 | CGTTCTCTTGTTCTC[A/G]TCTTTTTGGCCAAGA | 26259 |
rs760139525 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025736 | CCAGGTGGTGCCAAA[C/T]GGCAACTAAAACTCC | 26259 |
rs760139594 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004360 | TGTTTTTCTGTCTCA[C/T]ATATGATATATCACT | 26259 |
rs760228630 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116958573 | CCCCCCTGGTCATGG[C/T]GAGTTTATAGGCTGC | 26259 |
rs760233320 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116989154 | TTTGTATACTAAAAA[C/T]ATATTGTTGTAGAGA | 26259 |
rs760270723 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956049 | TCATAAGGCTAAAGC[A/T]TTCTAGTTGGCATAA | 26259 |
rs760278250 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019086 | ACGCATGCCTAAGGA[A/T]AGGTGTCTGTAAACG | 26259 |
rs760305395 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943238 | TTGACTGCCTTTTCC[C/G]CTGTGTATGGGCCCT | 26259 |
rs760346902 | snp | A/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984229 | AAAAGCATAAGCTCC[A/T]GTAGACCACTGGTCC | 26259 |
rs760350390 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000681 | TGAATCCTGGTGCCA[A/G]AACTTCCTAACTGGG | 26259 |
rs760374559 | snp | G/T | 6.61015e-05 | 0.0057486 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964792 | AGGATGAGCCTGGAA[G/T]GCAGCCAAATGTCTC | 26259 |
rs760449158 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925099 | AAAAAGATTGAACTT[C/T]TCAAAAAATAGATTC | 26259 |
rs760453887 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955130 | CCAAGTGTGTAAGAA[A/G]GGAAAACTCCCCTTC | 26259 |
rs760460414 | snp | A/G | 1.75891e-05 | 0.00296551 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985197 | CCTGCATTGTTTCTT[A/G]CTGCATAGGGTTTCT | 26259 |
rs760511706 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116999791 | TCCAGCCAGGCCAGC[A/G]CCATCCTCAATGTGC | 26259 |
rs760514136 | snp | C/T | 3.29788e-05 | 0.00406058 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028142 | TCACTACTACGACCT[C/T]GCACTGGCCTTTCCC | 26259 |
rs760550761 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022443 | GTAGATCCCTTGGCC[A/C]AGGAGTTCGAGACCA | 26259 |
rs760565809 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981223 | CTGATAAATTGACCA[C/T]TTATAAAATTAGCTT | 26259 |
rs760584211 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988783 | CTCCTTTACGCCCAC[A/G]GCCCGCCTGTCACAT | 26259 |
rs760588207 | snp | A/C/G | 0.000396507 | 0.0140748 | synonymous-codon, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028043 | ACACCGGGGGCTGAT[A/C/G]CGCGCCTATGAGTTT | 26259 |
rs760590915 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023736 | ACCGGGTCCTCACCC[A/G]GTTAGGATCTGGGGT | 26259 |
rs760592723 | in-del | -/AAA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954112 | GGGCGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 26259 |
rs760609562 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998663 | TAGTGTTAAAAATCA[C/G]CTCGTTCTCCAGTTC | 26259 |
rs760623498 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936017 | AAAAACCAGCTTCTC[A/T]GAGAGCTTCCATTGT | 26259 |
rs760644932 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990352 | AAGATGTGTCATGAT[A/G]TTACTCCTGAGTTTT | 26259 |
rs760649225 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927716 | GGTGATTCCTGTGCC[A/G]TATACCAGGCTGGAA | 26259 |
rs760674088 | snp | G/T | 1.69882e-05 | 0.00291441 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988889 | ACAACTAGCAAGATA[G/T]ATAATTAACAAAAAA | 26259 |
rs760678727 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116949290 | ACTTGCCACTCCCAG[C/T]AGATACATGCCAGCC | 26259 |
rs760682742 | snp | A/G | | | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032908 | CGCTTCCCACCACAC[A/G]TGTTAGATGGCAGAC | 26259 |
rs760704146 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969881 | ATTTTTTGAATTCCA[A/G]CCCTCTGGCCTCATA | 26259 |
rs760720983 | in-del | -/TT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929720 | CTTAAAATCTATCTC[-/TT]AGTGATTTTCAAGTA | 26259 |
rs760745222 | snp | A/G | 8.24042e-05 | 0.00641836 | missense, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024287 | CCGTGTGGGATTATC[A/G]GATGAACCAGAAGCT | 26259 |
rs760766306 | snp | A/G | 3.29554e-05 | 0.00405914 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985310 | CAGGACGATGCAACC[A/G]TGGCCACAGCTTCTG | 26259 |
rs760784951 | in-del | -/T | 0.476384 | 0.106067 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928004 | TTATAAACTTCTTTC[-/T]TTTTTTTTTTCCCCT | 26259 |
rs760805059 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002288 | GACGCTCAGCAACAC[C/T]GTCCCATCCCTGAAA | 26259 |
rs760821795 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977104 | AAGTGAGATGTTAGG[C/T]TGTCTGTGGTTTCTG | 26259 |
rs760831929 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000615 | CCACACTTTGAGCAC[C/G]CTGGGGTAGAGGTTT | 26259 |
rs760910615 | snp | A/G | 4.94181e-05 | 0.00497057 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949699 | CACGATGGTGTGGTC[A/G]TTGCGGGGTAAGCCA | 26259 |
rs760912628 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926984 | TGCAATACATAAGAC[C/T]GCTGTATTTGAGTGG | 26259 |
rs760912702 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970216 | TCTTTGGTGAGAAAT[G/T]AGATTACACACTTCT | 26259 |
rs760938640 | snp | G/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984576 | CCAAAATTCCAAAAT[G/T]CTTTGAAACTGTTTA | 26259 |
rs760944339 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937471 | CTGCCAGGCAGGAAG[A/G]AAACCCAGATGTGTC | 26259 |
rs760985582 | in-del | -/T | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988161 | ACTACAGTTCATGAA[-/T]AACCTTGTACATAAT | 26259 |
rs761014589 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996019 | GAGGGTTAGAAGACC[A/G]AATTGCCTTGTTTAA | 26259 |
rs761016456 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003876 | TTGTCTTTAATTTTC[A/T]GTGGTTTCATGCCAA | 26259 |
rs761022231 | in-del | -/C | 1.66294e-05 | 0.00288347 | frameshift-variant, intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985394 | GCGGAATTTGAAGTT[-/C]CGAAACTGGTGAGCT | 26259 |
rs761039017 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920746 | CTGTTGCCTTGATCA[C/T]TTGTAATGATCTTAA | 26259 |
rs761055530 | snp | C/G/T | 1.65233e-05 | 0.00287426 | missense, splice-acceptor-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985377 | GGTACTGGCAGATAG[C/G/T]TGCGGAATTTGAAGT | 26259 |
rs761091979 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937598 | TGACCATTGGGTTTT[C/G]CAAGTTGGAGGTCAC | 26259 |
rs761099021 | in-del | -/GCT | | | intron-variant, nc-transcript-variant, cds-indel | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977998 | TATTTTGGTGATCTC[-/GCT]GCTTTGTTTATGCCC | 26259 |
rs761140408 | snp | C/T | 1.66131e-05 | 0.00288206 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928059 | TTCTTTGATATCCAA[C/T]TGCCTTACGAATTGG | 26259 |
rs761154152 | snp | C/T | 1.6507e-05 | 0.00287284 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028166 | CTTTCCCTATAACCA[C/T]GTTTAGGGATGTGCC | 26259 |
rs761209565 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962802 | TCTGTTGTGTCTCTG[C/T]AGCTAAGCAAGTGGC | 26259 |
rs761211033 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995166 | GTGTAGCATGACTGA[C/T]AGCCCTATCCGGCCA | 26259 |
rs761230198 | snp | C/T | 1.6604e-05 | 0.00288127 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928151 | TCACCAACAGATGTT[C/T]CAGATTTTCCTAAAT | 26259 |
rs761239405 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963033 | GCTGGGCTTAAGGAC[A/G]TTCATCTTGTGTTTC | 26259 |
rs761247067 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964465 | TCTTATTATTGTTTT[C/T]TCATTTGAAATTGTC | 26259 |
rs761270391 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932102 | TGAGGTGATCACATC[A/G]TTTTTCTCCTTCATT | 26259 |
rs761329243 | snp | A/C | 8.2392e-05 | 0.00641788 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985299 | TAGCCCTCAGCCAGG[A/C]CGATGCAACCGTGGC | 26259 |
rs761332150 | snp | A/T | 0.000120847 | 0.00777231 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988895 | AGCAAGATATATAAT[A/T]AACAAAAAAGAATAT | 26259 |
rs761351196 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996168 | GCATTTGATGGCAGA[C/T]TGTATTAAGCGGCAC | 26259 |
rs761371880 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933224 | ATGCTGTTAGCCGAA[A/G]TCTTGGAACAGGGTC | 26259 |
rs761377956 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964110 | GCAAAACCGGGCAGT[A/G]TCGCGCATTCAGCAA | 26259 |
rs761382532 | in-del | -/TTTTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915643 | CTCACCTGACTACTT[-/TTTTT]TTTTTTTTTTTTTTT | 26259 |
rs761383379 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976338 | CTCTTTTTTGTATCT[-/TG]CTATTTGTCTTCAAG | 26259 |
rs761393468 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020450 | GCACTCTGTTTTTCT[C/G]CTTCCGGAACTTGGG | 26259 |
rs761396941 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029759 | GGATTACAGGCGTCC[A/G]CTACCACAACTGGCT | 26259 |
rs761398042 | snp | A/C | | | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977448 | CAAATGGTTATTCTT[A/C]AAAATCTTTTATTGT | 26259 |
rs761417174 | snp | A/G | 3.32546e-05 | 0.00407752 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928038 | AATGAAATGAATGAT[A/G]TGCCTTTCTTTGATA | 26259 |
rs761446994 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932187 | ATGGGTGTATGATTG[A/C]TAACCATTTGGCCTT | 26259 |
rs761479409 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019496 | TATCTATTCACTTGG[A/G]TTGCCTTGTCAGTTA | 26259 |
rs761485910 | in-del | -/AAAC | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987696 | CAGTTCATTGTAAAC[-/AAAC]AAACAAACAAACAAA | 26259 |
rs761496698 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990220 | TCATCTCAATGTGAA[-/C]ACTTTATCATCTCAC | 26259 |
rs761515590 | snp | C/G | 0.000355492 | 0.0133274 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911121 | GAAGAAGCGGCGACG[C/G]CCCGAGGCTGCCGAG | 26259 |
rs761515903 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990187 | AGACTAAGCGGTAGA[C/T]GATATGTGTGGCATC | 26259 |
rs761538778 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026121 | TGGTCACTGTCATGT[A/T]CCTCCCGCTGTCCGC | 26259 |
rs761578917 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930879 | GTGGTACAATCGTAG[C/T]TCACTGTAGCCTCAA | 26259 |
rs761613466 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912912 | CTAATTCGAATATAA[C/T]AATCCTGTGAGGTAG | 26259 |
rs761643713 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913913 | CCCCTTCAGAATCAC[C/T]ACATTAGGTACTACT | 26259 |
rs761679033 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989381 | GCAATGCTACAATGC[A/G]TATTGCAGCTTGCAG | 26259 |
rs761704140 | snp | C/T | 1.64836e-05 | 0.0028708 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010326 | TTCCTCTCTCAGATC[C/T]TGGTGTATAGCCTGG | 26259 |
rs761710901 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028692 | CCTTCCAGTAGCAAG[C/T]TGGTAGAGCTGTACT | 26259 |
rs761765250 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000756 | GGGAGTAAAATCATG[A/G]TACCTATCTTACAGC | 26259 |
rs761774998 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918243 | AAACCCAGGCTTCTT[A/G]GAGATAGTGGATATA | 26259 |
rs761799303 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947997 | TTCTGTGCTGTGCGT[G/T]CTCGACTTCAGGATG | 26259 |
rs761811567 | snp | G/T | 1.65048e-05 | 0.00287265 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988657 | ACAACTCTTACCTTT[G/T]AACAGGTTCAGTACC | 26259 |
rs761838083 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031820 | CGGCATATTGCTGGC[C/T]ATAAAAACTTCACCA | 26259 |
rs761841902 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024537 | GTGGGGATGCAGTTC[C/T]TGTCTCTGACATCAT | 26259 |
rs761855150 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936920 | CAAGGGCTGCCCTAC[A/G]TTTAAAAAGGGACCA | 26259 |
rs761855383 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116993307 | CGAAGTTTCACCATG[G/T]TGGCCAGGCTGGTCT | 26259 |
rs761857648 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979634 | GCAATCCCAGCACTA[C/T]TCAGAATTAATCATC | 26259 |
rs761872700 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932057 | TATCATGAAAGGATC[-/T]TGAATTTTGTCAGAT | 26259 |
rs761904700 | in-del | -/G | 4.94311e-05 | 0.00497123 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988714 | TACCCTGTGGCAGTA[-/G]CCGCTGCTGGAGATC | 26259 |
rs761945493 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991804 | GTCCAAATGTTGAAA[C/T]TGACTTTTAGTCAGA | 26259 |
rs761994331 | in-del | -/GGCCA | 3.30237e-05 | 0.00406335 | frameshift-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027438 | CCACAGCCTCATCAC[-/GGCCA]GGCCAACGTGCCTTA | 26259 |
rs761994672 | in-del | -/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116974802 | TAGTGCCCAGATTTT[-/G]GGTTTCTAAATGTTC | 26259 |
rs762005409 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946998 | AGGCTTGAATTCGAA[A/G]ATGTCAGACCGTGGT | 26259 |
rs762020122 | snp | G/T | 1.64814e-05 | 0.00287061 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010448 | TGGCAACATGGACGG[G/T]AGGTACGTGAGTTGG | 26259 |
rs762033917 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003186 | TTGTATGCGTGAAGC[A/C]TGTCTTTACTGTAAG | 26259 |
rs762047491 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001945 | CCACAAAGTAGGCCT[A/G]GCCTTCCTTTATTAT | 26259 |
rs762071426 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927074 | ATGGATTTTATTAAG[C/T]GAGTGCTGTTGGGAC | 26259 |
rs762081094 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030990 | CAGGGACGCCTCCAT[C/T]CCCGGCTCCCCTAAA | 26259 |
rs762083685 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984685 | ACTTTGCTTCATGCA[C/T]AGAATTATTTAAAAT | 26259 |
rs762102134 | snp | A/G | 1.66983e-05 | 0.00288944 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024365 | TTCCTAGTAGGAACA[A/G]GGAAGGCAGCACTAA | 26259 |
rs762130252 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014927 | GGACTCCTATCCCTT[A/C]CAGTTCTCTGGTCAG | 26259 |
rs762143159 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973476 | GTGATCACATTTAAC[A/G]TCATCAGTAATGGTA | 26259 |
rs762159745 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959198 | TTTTTGTTGGCTTCT[C/T]GCCTTCCAGTTGCAA | 26259 |
rs762161836 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973014 | GAAGAAGTGCTTGAA[A/G]AATGATGACAACATG | 26259 |
rs762223542 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985587 | TTACCAAGAAGCCAC[C/T]TCAGGCTGCTTAGAG | 26259 |
rs762319201 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026960 | CTATGAGCAGGATGT[A/G]GGGGGCACCTTCATG | 26259 |
rs762331795 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983838 | CCATCTTCAGTGCTT[C/T]GTGTGGCCGGTCTCC | 26259 |
rs762372396 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935487 | TTCTTCACTTTCACC[C/T]TTGCCGCCAGACTTC | 26259 |
rs762374069 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960551 | ATTTAGCTTATCCCC[G/T]GTTTTATAGTTTTTA | 26259 |
rs762402684 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025567 | TTACATGCAGAATGG[A/G]CTTCTTCCTTGGAGG | 26259 |
rs762409604 | in-del | -/AA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018438 | TTCCCAGCGTCGAGT[-/AA]ATTTGGTTTGAGTGC | 26259 |
rs762425066 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951473 | TTAAAGAGACAGTGG[C/T]CAACTCACCCCTTCT | 26259 |
rs762437071 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007296 | AGAGAACTTTCTGCT[-/A]AGAGTTCTTTTTAAA | 26259 |
rs762454688 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116952579 | CCTAGAGACGGGACC[A/G]TCTACAGCTGACAGG | 26259 |
rs762469591 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922482 | AGAGAGATCTTTCAT[A/G]TCCTCTTTGCCCTGG | 26259 |
rs762490065 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025921 | GCTAAGGAAGGCCTT[-/C]CCCAGAGGTGTGGCC | 26259 |
rs762502180 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116945849 | TGACTTTCACCGACT[C/G]TCTGGAGGGACCCAG | 26259 |
rs762537153 | in-del | -/AG | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116976993 | ATCCACTCTGGGCAC[-/AG]GGGAGGGAGACCCGA | 26259 |
rs762547218 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021362 | AGACATTAGCCCTTT[C/T]TGTTGCAAACATTTT | 26259 |
rs762557114 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943337 | TGGAAATAGAATCTT[G/T]CTCCCTCTTCAGAAT | 26259 |
rs762568470 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965385 | TTGTACATGAACAAC[C/T]ATGGATTTTTGGAAC | 26259 |
rs762577736 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010345 | TGTATAGCCTGGAAG[C/T]AGGACGCCGCCTCTT | 26259 |
rs762581348 | snp | C/T | 3.29625e-05 | 0.00405958 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010454 | CATGGACGGGAGGTA[C/T]GTGAGTTGGAAGGGC | 26259 |
rs762657975 | snp | C/G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964326 | GTGAGTGAGTGTGTG[C/G/T]GTTTGTGGGTAAATA | 26259 |
rs762672210 | snp | A/G | 6.59337e-05 | 0.0057413 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028102 | CTCTCCCTGTCTGCC[A/G]TTCATCCTGTGACGC | 26259 |
rs762712454 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964980 | ACACACATGTTCACA[A/C]ACATACACTCACTCT | 26259 |
rs762730882 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971358 | GAGCAAGACCCAGTC[-/A]AAAAAAAAAAAAAGG | 26259 |
rs762743179 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989523 | GCATAAAAGTGCATT[C/T]TGATGCTCTTTGAGC | 26259 |
rs762766102 | snp | C/T | 1.71076e-05 | 0.00292464 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027355 | CAAGTGCAGGCCCAG[C/T]GGACGCCCCCTTACG | 26259 |
rs762785037 | snp | A/G | | | synonymous-codon, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945423 | GTACAGGCTGTGCCA[A/G]CAGGAAGGGCACCTT | 26259 |
rs762800303 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913963 | TACAACTTTTGGGGC[A/T]CCTCTAATTTTAAAG | 26259 |
rs762902604 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915237 | GGTGTTGCACATTAG[A/G]TCTTTTCTCCCAGCT | 26259 |
rs762945930 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994843 | ACAACACTTGGTCCA[C/T]ATGAATGTATTTGTA | 26259 |
rs762957750 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927411 | GAGAGCATTAGGAAA[C/T]CTTGCACTTCTCCAG | 26259 |
rs762991020 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926829 | TGCTCTGGGCTGTCT[C/T]TTAGCCCCGAGACTT | 26259 |
rs763004362 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982372 | TTCAAAGCAAAGACT[A/G]TAGTAACCAGGGATA | 26259 |
rs763022606 | snp | A/C | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981421 | TAATTACATGGATAA[A/C]TAGAAATGGCTTTTT | 26259 |
rs763125957 | snp | A/C | 1.65007e-05 | 0.00287229 | synonymous-codon, stop-gained, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945514 | AAGGAACACATGTTA[A/C]GAACCAACTGGAAGG | 26259 |
rs763147248 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971673 | ATTTTGGGTGAGAGC[C/T]GTGAGATCTGTAGGA | 26259 |
rs763172747 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116949436 | TATGGTAACTCGCCC[A/T]TGCTTAACAGCTTAG | 26259 |
rs763182680 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020326 | GGTCTTTGTGTTTCC[C/G]CATTTTTTAAATTAT | 26259 |
rs763213984 | snp | C/T | 4.94466e-05 | 0.00497201 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028100 | CCCTCTCCCTGTCTG[C/T]CGTTCATCCTGTGAC | 26259 |
rs763232954 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018765 | TTTATTTTGTTTGGA[A/G]CCATCCATGCTGGTA | 26259 |
rs763233036 | snp | C/T | 6.59674e-05 | 0.00574277 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988669 | TTTTAACAGGTTCAG[C/T]ACCTTGAAATAGTTC | 26259 |
rs763234330 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973149 | ATAAAATAGGAATAT[A/G]TGAGTATATCATGAT | 26259 |
rs763266975 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941062 | AAATAGATTTCTTCA[A/G]AAGGGCAAAATCAGG | 26259 |
rs763278781 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116961288 | ACAGGCATGAGCCAC[C/T]GTGCCCGGCCTGTAT | 26259 |
rs763287994 | snp | G/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917071 | TCTGCATAGGTCATG[G/T]TTGTTATTCTCATGT | 26259 |
rs763296345 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116948077 | GACCCTAGAAGGGAC[A/C]CCAGGGTTCTCAGGT | 26259 |
rs763321710 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988765 | GAAGACTCCGCCAGA[A/G]CCCTCCTTTACGCCC | 26259 |
rs763321869 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945419 | TGTGGTACAGGCTGT[A/G]CCAGCAGGAAGGGCA | 26259 |
rs763343525 | snp | C/T | 0.000314864 | 0.0125432 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024138 | TCTGCTCTTCCTGGG[C/T]CTGTCCAGGGTGAGG | 26259 |
rs763344661 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117005443 | AGTTAGGAACCTTAG[A/C]GTTGAAACCTAGGAG | 26259 |
rs763344926 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004739 | GGGACCCAACTGTAG[A/G]TTCTACTTCATGCTG | 26259 |
rs763349145 | in-del | -/TGTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919685 | TAGGGGCCCTATCTA[-/TGTT]TGTTGAGTTGAAATA | 26259 |
rs763385940 | snp | A/C | 3.4313e-05 | 0.0041419 | splice-acceptor-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985204 | TGTTTCTTGCTGCAT[A/C]GGGTTTCTTAATATT | 26259 |
rs763429979 | in-del | -/AA | 1.64756e-05 | 0.00287011 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988774 | CCAGAACCCTCCTTT[-/AA]ACGCCCACGGCCCGC | 26259 |
rs763457072 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116957853 | ATGCTCTTCTGGTAA[A/G]TAAGTCTGAGGTAAG | 26259 |
rs763468035 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117006048 | ATGCTATTGTCTTGT[A/T]AGGAAGCCTTCCGAC | 26259 |
rs763471268 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017524 | TTCACCAAAGGCCAT[A/T]GTCAGTGCTTTGTAG | 26259 |
rs763521703 | in-del | -/T | 1.6823e-05 | 0.00290021 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028218 | AATGGGAAGAACCAG[-/T]TTTATCCATCTTAAA | 26259 |
rs763535097 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939496 | TTTTCTAAGGAACTT[A/T]TTAACACCTGGAGGT | 26259 |
rs763560387 | snp | G/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976135 | AAAAAGACTATCAAA[G/T]TACAGGATTAAATAA | 26259 |
rs763581022 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027049 | GCTCAAGGGACTTGC[A/C]CAGGGAGGCAGCGAT | 26259 |
rs763584146 | snp | G/T | 4.94368e-05 | 0.00497152 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024193 | ATCGCCCTGTCGCTC[G/T]CCGCCCATCAGCTCA | 26259 |
rs763617866 | snp | A/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909812 | ATGCTGTGAGAATGA[A/G]TAACAGGGATACCTG | 26259 |
rs763638591 | snp | C/G | 5.89936e-05 | 0.00543077 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911091 | GCAGGAGGAGCTGGC[C/G]CAGGCCCAGGCGCCG | 26259 |
rs763642073 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116961665 | TGAACAAAACCCAGA[C/T]CCTGAGCTCAGAAGC | 26259 |
rs763701209 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019371 | TTAATGTTGGCCACA[C/T]AGAATTTTATGTTCT | 26259 |
rs763727882 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921250 | AGCTGGTTAGATTCT[A/G]TAGTATTATAGTTCA | 26259 |
rs763749472 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116967624 | TGTGTGTTGTTAGCT[C/G]TTTCTATTTCTTTCT | 26259 |
rs763765313 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930865 | CAGGCTGGCATGCAG[C/T]GGTACAATCGTAGCT | 26259 |
rs763791179 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017698 | AAGCCTACATTGTAA[C/T]ACCTTATTGCTTGTT | 26259 |
rs763791199 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028613 | TGGCCTCCAAGGCAA[A/T]AACCTCCATGTCCTT | 26259 |
rs763806986 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027906 | TGTGTGCCCAGAGAA[C/T]GCGTTTGTGAAGCTG | 26259 |
rs763868345 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116967496 | ATTGCCCTCCAAAAA[A/G]GTTTCACCAGTTTAT | 26259 |
rs763871687 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947248 | TAGGTAAGTACTCAC[-/T]TACATGGCTGTTGAT | 26259 |
rs763943790 | snp | C/T | 5.12606e-05 | 0.00506238 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945564 | TTACCTGTGAAAGAA[C/T]AGCCTGCAAGGACAT | 26259 |
rs763945423 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941424 | GCTGTGAATTCCATG[C/T]GAAGTGTCCATGCCT | 26259 |
rs764036751 | snp | C/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981324 | AGATATCCAACAATA[C/G]AGTTCAAAGGGAAAT | 26259 |
rs764042041 | snp | G/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985322 | ACCGTGGCCACAGCT[G/T]CTGCTTTTGATGTCG | 26259 |
rs764104928 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998667 | GTTAAAAATCAGCTC[G/T]TTCTCCAGTTCATGG | 26259 |
rs764104948 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011921 | ATTTGCAGCAAGCCA[A/G]GTACTATGTTGAATC | 26259 |
rs764112332 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965852 | CATCCTCAACCTCCC[A/G]GGATCCAGTGATCCT | 26259 |
rs764122857 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990416 | GTTTCCTAAGGCAGT[C/T]TCCTTTCTCATGCTC | 26259 |
rs764190691 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010854 | CCTGCCAAACGATGT[C/T]AAGAGTGTATTTCAG | 26259 |
rs764191798 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926985 | GCAATACATAAGACC[A/G]CTGTATTTGAGTGGT | 26259 |
rs764193617 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946798 | TGCACACAGGCAGAA[A/G]GGTATGACAAAGAAA | 26259 |
rs764214377 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971788 | TGTGGGATCTCGGTA[A/C]CAGAATTTACACTTT | 26259 |
rs764218448 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116957851 | ACATGCTCTTCTGGT[A/G]AATAAGTCTGAGGTA | 26259 |
rs764248581 | snp | A/G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959177 | TGCTCCCAGCATACT[A/G/T]AGCCTTTTTTGTTGG | 26259 |
rs764289145 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030115 | AAGTGCTTGCCATTA[C/T]TCCAAAGCCTAGAAC | 26259 |
rs764329624 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915442 | GCCTAAATACACAGC[C/T]TGATGAATTTTCAAG | 26259 |
rs764342298 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971214 | CAAAAAATGAACTAG[C/G]TGGGCATGGTGGGGT | 26259 |
rs764356095 | in-del | -/TTGT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930511 | CTTCTTGCTATTGAG[-/TTGT]TTGAGTTCCTTATGT | 26259 |
rs764508584 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932793 | TGCCTCGGCCTCCCA[A/C]AGTGCTGGGATTACA | 26259 |
rs764516697 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995187 | TATCCGGCCAGTGTC[A/G]TGGTGGCAAGAAAGA | 26259 |
rs764524430 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937476 | AGGCAGGAAGAAAAC[C/G]CAGATGTGTCGTTCC | 26259 |
rs764549255 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117024803 | ACCATGGTTCTGCCC[A/G]TTGCTTAGACTTTCC | 26259 |
rs764580740 | snp | G/T | 1.66114e-05 | 0.00288192 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928158 | CAGATGTTCCAGATT[G/T]TCCTAAATGTGTGAT | 26259 |
rs764608761 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996183 | TTGTATTAAGCGGCA[C/T]ACGGCGTGCATCCTA | 26259 |
rs764615249 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962812 | CTCTGTAGCTAAGCA[A/G]GTGGCCTTACTCCAG | 26259 |
rs764615831 | snp | G/T | 1.64754e-05 | 0.00287009 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949742 | TGAGTGCTCTGCATC[G/T]GAAGGTCTTTCATTT | 26259 |
rs764630769 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920802 | AATTCTATAGCCAAT[C/G]CTGATGGTGGGAATG | 26259 |
rs764663339 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007815 | GCTCAACCTTATTAA[A/G]AGAGAGAGAGTGCGT | 26259 |
rs764667068 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007752 | AGTGTGAGCATGAAT[-/A]ATTAATCTCACTAGT | 26259 |
rs764685715 | snp | A/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982927 | CTCATCCTGCACTTT[A/T]CCAGCTAAATTCCAG | 26259 |
rs764697524 | in-del | -/CT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116958022 | CCACAGCTACAATAA[-/CT]CTGCATAATCATCAT | 26259 |
rs764708287 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964143 | GCTTTTCATGAGCAG[C/G]CAGCACTGTCTGGCT | 26259 |
rs764734488 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956367 | ATTCCTTTTGAGGCA[A/G]GTGTGCCCAAGTAGA | 26259 |
rs764748923 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983936 | CTCAGAGCTGTTAAG[C/T]AGCTCCCCTAAGTCC | 26259 |
rs764813349 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023654 | AGGCTTTCCCTTTCT[C/T]AGTTCCAGCAAGACA | 26259 |
rs764844529 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007890 | GTGGAAAGAACTGCC[G/T]TTGAGATGGGTAATG | 26259 |
rs764900411 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930994 | TAAATTTTTTGTAAG[A/G]ACAGGGTCTTGCTTT | 26259 |
rs764951953 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943661 | CAGAGGGGAGAGGTT[A/C]GGGCCTTCTCTGGTC | 26259 |
rs764958684 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019635 | TTTTAATTATGAAAC[C/T]GAACATATGTATGGG | 26259 |
rs765038413 | snp | G/T | 5.10304e-05 | 0.005051 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945314 | TTTTGGATGACAAGG[G/T]GCTTCTCTAATTGCA | 26259 |
rs765070729 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000851 | TATTAGCTGTTATTA[A/G]TAACTATTTTGGTAG | 26259 |
rs765090300 | snp | A/G | | | missense, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024307 | AACCAGAAGCTGTGG[A/G]AGGTGTATTCCGGGT | 26259 |
rs765093089 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013322 | TGGAAACTGAGTTAA[C/T]GTTAGAGTATGCTTT | 26259 |
rs765136531 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985329 | CCACAGCTTCTGCTT[C/T]TGATGTCGTGATGTT | 26259 |
rs765151874 | snp | A/C/T | 4.942e-05 | 0.00497071 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949718 | CGGGGTAAGCCAAAC[A/C/T]GTTTCCACTGAGTGC | 26259 |
rs765161927 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989384 | ATGCTACAATGCATA[C/T]TGCAGCTTGCAGAAG | 26259 |
rs765178343 | snp | C/G | 1.68369e-05 | 0.0029014 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024372 | TAGGAACAGGGAAGG[C/G]AGCACTAATCAGCCT | 26259 |
rs765184833 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968603 | ATGACATTTCACACA[A/T]GTGCAAGGAGGATTG | 26259 |
rs765187795 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912981 | TTCTCTGTAACTTGC[C/G]CAGCATTACCCCACT | 26259 |
rs765203134 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955382 | TTTCTCATTTCTGTA[A/G]CTTGAGAAAAATTTA | 26259 |
rs765224431 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000170 | TTTAGTAGAGACGTG[A/G]TTTCACCGTGTTAGC | 26259 |
rs765247317 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951775 | CATGATGGACCCAGT[C/T]ATGGTTCTTCCCTAC | 26259 |
rs765253489 | snp | A/C | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988016 | CATTTGTTTCGTTTT[A/C]TAAAGAACGTTTTCA | 26259 |
rs765262152 | in-del | -/G | 1.64754e-05 | 0.00287009 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988739 | AGATCTGATGTACCT[-/G]GCTCAAAGCCGAAGA | 26259 |
rs765312736 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935550 | TATGCTCAAGACCCA[A/G]GTGCCCTCAGGAGTT | 26259 |
rs765340091 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979675 | CTATTGAGGTTTGGT[C/T]AGGAAGGAAGAAAAA | 26259 |
rs765362733 | snp | A/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910415 | GTTGCTACGAATGCC[A/G]TGAATTCATTCCTTT | 26259 |
rs765379412 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003200 | CCTGTCTTTACTGTA[A/G]GGCCAGCATAGCAGT | 26259 |
rs765388061 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032007 | ACAGAATAAATGTTT[A/G]CAAAGCAAAAATTGT | 26259 |
rs765428598 | snp | A/C/G | 9.95318e-05 | 0.00705392 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028177 | ACCATGTTTAGGGAT[A/C/G]TGCCTCAGTTGGGAG | 26259 |
rs765431501 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018558 | TGTGAATCTGAATGG[C/T]TTGGGTGGACTTAGC | 26259 |
rs765443029 | in-del | -/TT | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982624 | TGATGGAGCCCTGGA[-/TT]TTTTTTTTTTTTTTT | 26259 |
rs765474318 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016512 | TTTAATATAGCCCAG[A/G]TACAAATCTCTCATC | 26259 |
rs765536773 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928485 | GCCCTTGGTTAAATC[A/G]AGCCTGTTATTAGGT | 26259 |
rs765555789 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994155 | CAGCATGGTACTGGT[A/G]GTAAAAGTAGATATG | 26259 |
rs765587885 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939472 | TAAGCTCATTTGAGC[A/G]TGGAATCCTTTTCTA | 26259 |
rs765599601 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959224 | TGCAATTTAGTGGTC[A/G]AATTGATGGGTTAGG | 26259 |
rs765658173 | snp | C/T | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964729 | TGAGAGTGTGGGACA[C/T]CCGCACCTGGGACTA | 26259 |
rs765675432 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983839 | CATCTTCAGTGCTTC[A/G]TGTGGCCGGTCTCCT | 26259 |
rs765699804 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951400 | TTGTGGTTACCTCAT[C/T]CCCAATCAATGTTGA | 26259 |
rs765711925 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977411 | AATTAACGTATTTTT[A/G]CTTTTGTTAGTGATA | 26259 |
rs765716766 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938950 | ATCTCTGTCACATGC[C/T]AAAGGTTTTGGTTTC | 26259 |
rs765745516 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996909 | TGTGGTCCTTAACAG[C/T]GACTTGGCGATGTAA | 26259 |
rs765747493 | in-del | -/CACCAA | 1.65899e-05 | 0.00288005 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928136 | GCACAGGTAAGGTGT[-/CACCAA]CACCAACAGATGTTC | 26259 |
rs765748934 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027092 | GTTGCATGTGGCTGA[G/T]TCGTCTGCAGTAGGG | 26259 |
rs765789388 | snp | A/G | 1.64811e-05 | 0.00287059 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010450 | GCAACATGGACGGGA[A/G]GTACGTGAGTTGGAA | 26259 |
rs765833793 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970360 | GTGCCATCAAGCACG[A/G]CAAAGTGGCTTATCC | 26259 |
rs765835554 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982182 | TAGATTAAACCCAAC[C/T]TTATGAATAATCACA | 26259 |
rs765859157 | snp | A/G | 3.29658e-05 | 0.00405978 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964685 | GGAACCAAGTGTGTC[A/G]TTCTCTTCCAGATAT | 26259 |
rs765861906 | snp | C/T | 1.64746e-05 | 0.00287002 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949731 | ACCGTTTCCACTGAG[C/T]GCTCTGCATCTGAAG | 26259 |
rs765922735 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939053 | CTTAACTGATTGACC[A/G]GTAACCCAAATCAGT | 26259 |
rs765949259 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026025 | AGGCTGACAGACACA[C/T]GGTCTCCTGCCCAGA | 26259 |
rs766001393 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116997246 | CTGATACTCTGTACA[A/G]CTGATGGGTTATTCT | 26259 |
rs766012340 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020723 | TGTTTGATGAAACCA[C/T]GGAGCTGAGCCTGGC | 26259 |
rs766020998 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922508 | CCTGGAGATGTACAT[G/T]GGGAACAAAAACCTT | 26259 |
rs766035039 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921141 | CCCAGGAGAGTGAGA[A/C]TATGTCTTGAAGCTG | 26259 |
rs766057999 | snp | C/T | 4.94254e-05 | 0.00497094 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010350 | AGCCTGGAAGCAGGA[C/T]GCCGCCTCTTGAAGC | 26259 |
rs766060034 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009424 | ACCAAAAACTTCTGA[C/G]TTCATTAATTTAAAA | 26259 |
rs766065066 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965429 | TCTAAAGTTAGCTTT[A/G]TCTATGCAAAGAAAC | 26259 |
rs766088358 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932428 | CAGCATATGAAGGCG[A/G]TTTGAGAGTGGTGAA | 26259 |
rs766103214 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969843 | TGGGGTGTTGAGATT[-/T]GGCAAGGTGATCCAC | 26259 |
rs766111617 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933588 | GGCCAGTTGGATTTG[G/T]CTTTTTGTTGTTGTT | 26259 |
rs766125861 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984256 | GTCCTAAACTCCAGT[A/G]GACATCCCCAGAGTT | 26259 |
rs766150088 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021399 | TTTATCATTGGACTG[A/G]CTTTCTGATTGTTCC | 26259 |
rs766156067 | snp | A/G | 3.30224e-05 | 0.00406326 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027443 | AGCCTCATCACGGCC[A/G]ACGTGCCTTACCAGA | 26259 |
rs766231928 | snp | C/G | 1.68499e-05 | 0.00290253 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985408 | TCCGAAACTGGTGAG[C/G]TTTTTAGTCTGGTCA | 26259 |
rs766233418 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002185 | TGCCTGCCCGGGAAG[A/C]GTCCAGTCCTGGAAC | 26259 |
rs766239603 | snp | A/G | 1.7105e-05 | 0.00292441 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027356 | AAGTGCAGGCCCAGT[A/G]GACGCCCCCTTACGA | 26259 |
rs766282971 | in-del | -/GC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943815 | GGTCAGCCTCTAACA[-/GC]CCCAGCTAGCAGTGC | 26259 |
rs766290090 | snp | C/T | | | synonymous-codon, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945468 | CTCTGACTATTCTTG[C/T]TGGAAGCTCATCTTC | 26259 |
rs766313332 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116958519 | TAGATTCATTCATTC[C/T]GTCAACACCCACTAA | 26259 |
rs766321669 | snp | A/G | | | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977945 | TGAGAGCTACTAAAT[A/G]TATTCAATCTTACTT | 26259 |
rs766323509 | snp | G/T | 1.64776e-05 | 0.00287028 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988705 | ACCAGAAGGTACCCT[G/T]TGGCAGTAGCCGCTG | 26259 |
rs766388283 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932570 | CTTTGACGGAGTCTC[A/G]CTGTCACCAGGCTGG | 26259 |
rs766391042 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030715 | AACGTACCTGCCATT[C/T]GTGGAAGTCGCCTGG | 26259 |
rs766452759 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915257 | TTCTCCCAGCTCATC[A/G]GGTGTTTTTATGTGT | 26259 |
rs766458684 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971352 | GCAACAGAGCAAGAC[C/T]CAGTCAAAAAAAAAA | 26259 |
rs766468730 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922811 | AGTGTGTGTGTGTGT[-/T]GTTTTTTTTCCCTTG | 26259 |
rs766483981 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030040 | ATGGGAACCGTTTGT[C/T]CACACTCATTCCAGA | 26259 |
rs766486077 | in-del | -/TAAG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935239 | TGACAGCAAAATAAA[-/TAAG]TAATTCTAGAACCAA | 26259 |
rs766544267 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116961321 | GCACTTTTTAAAGCA[C/T]TCCAGGCAAATTTAA | 26259 |
rs766560393 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023995 | TCCCTGACAGTCTGT[A/G]CTTGATGTCCTTATT | 26259 |
rs766580440 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991622 | AGTTTGCCTGGAGCT[A/G]TATCCACACTAGGGT | 26259 |
rs766582898 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929905 | GCTCAACTTTTTTAG[A/G]TTCTACATTTAAGTG | 26259 |
rs766599677 | snp | A/G | 1.70563e-05 | 0.00292025 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985206 | TTTCTTGCTGCATAG[A/G]GTTTCTTAATATTTG | 26259 |
rs766629669 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953441 | GCTATTATAGCATCA[G/T]TTTGGTTTTTCTTTT | 26259 |
rs766658881 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975330 | GGAGGCTGGAAAGTC[C/T]AAGATCAGGGCACTG | 26259 |
rs766664566 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117032228 | CCAGAGCCTATCCCA[A/G]CAGCTCAGTGTGCAA | 26259 |
rs766668567 | snp | A/G | | | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116918643 | ATTCCCATTGCTGCA[A/G]ACTGGGTCATGTGTC | 26259 |
rs766673206 | in-del | -/TCTA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116997408 | AGATAGCAGTTGTGT[-/TCTA]CACCACTGGAGACTG | 26259 |
rs766691499 | snp | C/T | 5.39127e-05 | 0.00519167 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911146 | GCCGAGAGGCGGGCT[C/T]GGCGGCCGGAGGTGG | 26259 |
rs766692509 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935695 | CATTGAGCTAAGTGG[G/T]GGGTACTTTGGAGTT | 26259 |
rs766718162 | snp | A/G | 3.74188e-05 | 0.00432528 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027524 | GTGGTGGGGCCGGGC[A/G]AGTAAGAGACCATCT | 26259 |
rs766725125 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992044 | TGTTCCTGGCATTGG[C/T]ATGTTAAAACAGCAT | 26259 |
rs766745798 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116948203 | GCCATAGTGTTTTTT[C/T]TCCTAGTGTTTGCAT | 26259 |
rs766793287 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929138 | TCTAAGCAGGGGATG[C/G]CAGTGTGGCTTTGGC | 26259 |
rs766812496 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971922 | TCTACAAGCCCTCAA[A/C]GTTAAGAAACACTGG | 26259 |
rs766819006 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960689 | CCCCTCAAGCCAGTC[A/G]GGTTGTTACCTGCGG | 26259 |
rs766828897 | in-del | -/A | 0.000104837 | 0.00723932 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988899 | AGATATATAATTAAC[-/A]AAAAAGAATATAGAT | 26259 |
rs766875217 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024195 | CGCCCTGTCGCTCTC[C/T]GCCCATCAGCTCAGG | 26259 |
rs766878922 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017614 | GCCCAGGTTCAGTGA[C/G]AGCAAACAGAATCAT | 26259 |
rs766887192 | snp | A/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985882 | TAAAGTAACTCTTGC[A/G]TGAAGATAGATTTAA | 26259 |
rs766966391 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027869 | GTTGACCGCTAAGCC[A/G]GGGACTGTGAGTATC | 26259 |
rs766971492 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017556 | TAAAGCTATTGATTT[C/T]GGCATATAAGGTTAT | 26259 |
rs766979072 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987682 | TGAATGTTATTTATT[C/T]AGTTCATTGTAAACA | 26259 |
rs767021361 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018881 | GTAAATTATGGAGTA[C/T]AAATATTCAACAGAG | 26259 |
rs767033214 | in-del | -/TA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937720 | ATAGAGAGCTGTCTC[-/TA]TATGTGGTGTGTCCT | 26259 |
rs767054947 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973439 | TGCAGTCAGGAAATC[C/T]AACAGGAACCGTCTT | 26259 |
rs767061996 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928592 | CCCTTTAAACTTTAG[G/T]ATCTCACTCAGTGAG | 26259 |
rs767083439 | snp | A/G | 1.65113e-05 | 0.00287322 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027448 | CATCACGGCCAACGT[A/G]CCTTACCAGACGGTA | 26259 |
rs767141584 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941376 | AAATGACAGCTTTGT[C/G]ACTTATTTATGCCAC | 26259 |
rs767169102 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116997413 | AGCAGTTGTGTCACC[A/G]CTGGAGACTGAGCAA | 26259 |
rs767189073 | snp | A/C | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986283 | ACTTTGAGTATAGTG[A/C]TCCCCTAAAATGGCC | 26259 |
rs767207143 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998461 | CAAATTAAGCTTAGA[A/G]TGTTATTTAGAGGCT | 26259 |
rs767265136 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965767 | CTTACATACATACCT[A/C]TATATATTTGAGACA | 26259 |
rs767267851 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939783 | CTGAATTCCAGGGCT[C/T]GGTTAGGGGACATAC | 26259 |
rs767324412 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009587 | ACACATAGGAAGCAT[C/T]TAATGTTCTTTGAAT | 26259 |
rs767367546 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935010 | TGATCTGTTCTCCAA[A/C]TCCATAATTTTGTTT | 26259 |
rs767370111 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010688 | TTTTCTTTTAAGCCA[C/T]TTGGTGGCCGCAGTT | 26259 |
rs767371028 | in-del | -/AGAG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019106 | GTCTGTAAACGTGAC[-/AGAG]AGAGACCTTTGTTTA | 26259 |
rs767378488 | in-del | -/T | 5.50727e-05 | 0.00524722 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928000 | AAAATTATAAACTTC[-/T]TTTCTTTTTTTTTTC | 26259 |
rs767397308 | snp | A/G | 1.67511e-05 | 0.00289401 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945532 | ACCAACTGGAAGGTG[A/G]GCAGTGGCCAATATC | 26259 |
rs767423151 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933829 | AGTAGCACTTTCATT[C/T]GTTTCTTGGGGTGTT | 26259 |
rs767487045 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964526 | TCACAGCCTTCTGTC[A/G]TCTAGTTGACATTTT | 26259 |
rs767490011 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937036 | AGAAGAGGATGTGGT[A/G]CTTGGGCCAGGATGG | 26259 |
rs767503773 | snp | A/G | | | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978325 | CTTTATGCTAGTTTT[A/G]TGTCTCTGGCCTGCA | 26259 |
rs767531087 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953364 | GTTTCTGCAGCATCC[A/G]CAGGCAGGGCTGGCT | 26259 |
rs767558423 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969786 | AGTCATCCCTGCATC[A/C]CTTTTAGCCTCTTTG | 26259 |
rs767614359 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937067 | CACCAGCAGAAGTGG[A/T]CAGAGTCAGGATTGT | 26259 |
rs767632750 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968925 | CGTCTTGGATTAGCA[C/T]GCAGTATGGTTCCAA | 26259 |
rs767638133 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029011 | AAGCGAAAACTGATA[A/G]AACTACAAAGAGAAA | 26259 |
rs767643703 | snp | C/T | 1.64803e-05 | 0.00287052 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024282 | GGTGTCCGTGTGGGA[C/T]TATCGGATGAACCAG | 26259 |
rs767651236 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982500 | GTGATATCAGCCCCC[C/T]GACAAGTGAGGATCT | 26259 |
rs767664420 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013769 | TTATTTTTTATTATC[A/G]TCAGTGGTGTTTTCA | 26259 |
rs767687463 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969968 | CACTAATTGTGTTGC[A/G]CGTTACCATACCGAA | 26259 |
rs767735080 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950505 | GACTTTAAAACTCAG[A/T]AGTAGAGGAGTCCTT | 26259 |
rs767775143 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926336 | CTCTTGTTTCTTTAC[C/G]AAGTAGGTAAAGTAG | 26259 |
rs767784516 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024694 | AAACATAGGAAGCTC[A/G]CTGGGCTAGACCAGG | 26259 |
rs767828566 | snp | G/T | 2.20772e-05 | 0.00332237 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988919 | AGAATATAGATTTAT[G/T]TTTTAGAAGGGAATT | 26259 |
rs767830758 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116972234 | AGTAGCACAAGGTAG[C/G]TTTGGGGAGATAGTT | 26259 |
rs767848924 | snp | G/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983523 | CCAAATGTATTATTT[G/T]CTTCCAATTCTCTAT | 26259 |
rs767883293 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000158 | GCCTTTTGTATTTTT[A/G]GTAGAGACGTGGTTT | 26259 |
rs767886626 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981681 | TGCAGTGGCACTATC[C/T]TGGCTCACTGCAACC | 26259 |
rs767903175 | snp | C/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910784 | CAGAGCTTAGCAAAA[C/G]TGATAGGCAGCAGAG | 26259 |
rs767933066 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913289 | CATTGATGCCAAAAA[C/T]AGTAAAGAAGCAAAT | 26259 |
rs767946556 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116961500 | GCTGGGGAGAGGGGT[A/G]GAAGTTAGTTTGTGG | 26259 |
rs767955221 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995077 | TCTGACTGGTCCTGC[A/C]CTTCATTTAAATTAT | 26259 |
rs767961305 | snp | A/G | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028053 | CTGATCCGCGCCTAT[A/G]AGTTTGCGGTGGACC | 26259 |
rs767986510 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919564 | TTTTACTTCCTCTTT[A/C]CTGAAGCTTATCACC | 26259 |
rs767993065 | snp | G/T | 0.000214223 | 0.0103472 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985286 | AGAATACAGGCACTA[G/T]CCCTCAGCCAGGACG | 26259 |
rs768008339 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117006861 | TTTTATCTAAAAATT[-/A]TAAACAATCCATATG | 26259 |
rs768020293 | snp | A/C | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985305 | TCAGCCAGGACGATG[A/C]AACCGTGGCCACAGC | 26259 |
rs768051529 | snp | C/T | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028107 | CCTGTCTGCCGTTCA[C/T]CCTGTGACGCCATGG | 26259 |
rs768078394 | snp | C/T | 0.000271444 | 0.0116468 | intron-variant, missense, utr-variant-5-prime | FBXW8 | GRCh38.p7 | 12:116911170 | GAGGTGGGCTCCGGG[C/T]GCGGCGAACAGGCCT | 26259 |
rs768102137 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020402 | GCATGCATGTCTTTC[A/G]TCAGTTCGGGAAACA | 26259 |
rs768107982 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030490 | GTCTTAATGCGTCTG[G/T]ACCACTGGGGAAAAT | 26259 |
rs768176903 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116957066 | AATGTACCTTGTTAT[A/T]AGCCGGGCACAGTGG | 26259 |
rs768180467 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935508 | GCCAGACTTCTCTTA[C/T]CAGGAAGTTCTGTGG | 26259 |
rs768185404 | snp | A/C | 1.64779e-05 | 0.00287031 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024252 | GAAGATCGTCAGTGG[A/C]GGCGAGGAAGGCCTG | 26259 |
rs768185448 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116989158 | TATACTAAAAACATA[C/T]TGTTGTAGAGATGGG | 26259 |
rs768202045 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116914947 | AAGTTATAATTCATT[C/G]TGTGCGTAAACTGTC | 26259 |
rs768220269 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926652 | AGATTTTTTTTCCTG[A/T]TTTTTTCTGTATGGT | 26259 |
rs768273408 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937902 | GCTATAAAGCAAAAT[G/T]CTGGAGACACTTTTA | 26259 |
rs768290044 | in-del | -/GCT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913621 | CATGCTGGGTAGGCT[-/GCT]GCTGCTGCTGCTACG | 26259 |
rs768310872 | snp | A/G | 3.32579e-05 | 0.00407773 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928036 | AGAATGAAATGAATG[A/G]TGTGCCTTTCTTTGA | 26259 |
rs768404727 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969379 | ATTCTTTCCCCAGAC[A/G]TCAGGTGGCGTTACC | 26259 |
rs768440210 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925934 | TTGCTCTGAACCTCC[A/G]TGCTGGGTTGCATCC | 26259 |
rs768445140 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116931868 | GCCTAATTGCTGTGA[C/T]TAAGACTTCTAGTAC | 26259 |
rs768450375 | in-del | -/C | 1.69258e-05 | 0.00290905 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027369 | GTGGACGCCCCCTTA[-/C]GAGCTCTCTCCCACT | 26259 |
rs768453104 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936207 | AAGGACACTGTGCAG[A/G]TCTCTGGCAGAGTGG | 26259 |
rs768466500 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926615 | TTAGGCAAGCACCCC[-/T]GAGCCTTCTAATTAC | 26259 |
rs768476081 | snp | C/T | 8.23689e-05 | 0.00641698 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010380 | CTGGGTAACGTTCTC[C/T]GTGACTTCACGTGTG | 26259 |
rs768494636 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983123 | CAGAAGCTCTATGCA[A/G]ATGGGAGTTTTTTTT | 26259 |
rs768538041 | in-del | -/CA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964962 | ATATGTACACGTGGG[-/CA]CACACACATGTTCAC | 26259 |
rs768545300 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023779 | AGCTCTTGCCTTTAA[C/T]AGGTTATTTTACCAA | 26259 |
rs768550818 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968354 | GAGTGTGTATATTCT[C/T]ATTGCCCCCTTTTTA | 26259 |
rs768552886 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933943 | TCTCTCTCCATCTCT[C/G]TTTTAATCTAGGTGC | 26259 |
rs768558983 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936859 | AGAACTCGAAGTTTT[G/T]TGAATAAGATGGGAA | 26259 |
rs768569307 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995421 | TGAGCCAGTCCACTG[A/G]AGGATGCTGAGTTGC | 26259 |
rs768580987 | snp | C/T | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028092 | TTCCAGAGCCCTCTC[C/T]CTGTCTGCCGTTCAT | 26259 |
rs768581992 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017308 | CCATCTAATGCCGGT[C/T]CAGAAAGGTTCAGTG | 26259 |
rs768613631 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955678 | ATCCTTGAGGAGAAA[A/G]AGTAGAAGAAAGGGG | 26259 |
rs768690633 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950058 | ATAATAAGTGTTGGC[A/G]CAGACAGGCCCTGTT | 26259 |
rs768765571 | in-del | -/G | 3.34622e-05 | 0.00409023 | frameshift-variant, intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985402 | TGAAGTTCCGAAACT[-/G]GTGAGCTTTTTAGTC | 26259 |
rs768772645 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117015629 | ACTGGGTTGCTAAGT[C/T]ACTGAGCCAGCAAAT | 26259 |
rs768787475 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116940592 | GGAAGAGAATGTGAA[C/T]GGTGAGAGATACTCA | 26259 |
rs768794629 | in-del | -/AG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937111 | GTGGGGACAGAAGGA[-/AG]AGAGTCAACAAGGGC | 26259 |
rs768840385 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954216 | TCAAATTCTAGCATG[G/T]AACACAACCTTTATT | 26259 |
rs768896244 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117015910 | GATTTGCCTGAACAT[A/C]TCCTATAAATGAAAT | 26259 |
rs768964915 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116952222 | CATTCATGTACCCTA[C/G]GTGTATAGTAGGCTC | 26259 |
rs768977661 | in-del | -/CTTGATGGTTTTTTA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995618 | TAGGAAGAAGGGCTG[-/CTTGATGGTTTTTTA]CTTTTGGACAAAAAT | 26259 |
rs768984435 | snp | C/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978833 | TTTCCAAAACCAGTT[C/G]AGCAGTTATTTACCT | 26259 |
rs768992692 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938661 | ATTTGCACAGTCCTC[-/A]ATGAAAACTCATACA | 26259 |
rs769027337 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009171 | GAGCTCAAAAGTTTG[A/G]GACCCGGCTGGGCAA | 26259 |
rs769034332 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963443 | TCTCTACTAAAAACT[-/A]AAAAAAACAAACTAG | 26259 |
rs769037612 | snp | C/G | 3.30278e-05 | 0.0040636 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988648 | TGGGACTAAACAACT[C/G]TTACCTTTTAACAGG | 26259 |
rs769038555 | snp | A/G | 1.6483e-05 | 0.00287076 | synonymous-codon, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945486 | GAAGCTCATCTTCCA[A/G]GAGTGCCGAGCCAAG | 26259 |
rs769071593 | snp | A/T | 3.30251e-05 | 0.00406343 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964787 | CGAGGAGGATGAGCC[A/T]GGAATGCAGCCAAAT | 26259 |
rs769091710 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963851 | AAAGGCATTTCTCAC[C/T]ACTTTTCCCCCCATA | 26259 |
rs769106863 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117010224 | CTTCACGGGAGCTCA[A/G]TGATAAGGATCATGC | 26259 |
rs769131698 | snp | G/T | 1.65899e-05 | 0.00288005 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928096 | ATATATTTCAGTATC[G/T]GGACAGGAAAGAACT | 26259 |
rs769143909 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025765 | CCCGCACTGAAATTC[A/C]CGGAAGCATTGCCTT | 26259 |
rs769154920 | in-del | -/TGG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018159 | GTCTTTTGTTTTAAT[-/TGG]TGGGCTACCGCCGAC | 26259 |
rs769159458 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021117 | ATGTCTCCCTGCCAC[A/G]CAGTGCCTCGTAGGG | 26259 |
rs769233469 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977382 | GTGGCTGTTGAAAAC[A/G]TTTGTAAAACACAAA | 26259 |
rs769251484 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009259 | TCAGCAGGCCGTGGT[A/G]TTACACACACATGGC | 26259 |
rs769253004 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933165 | TCCCAAGAGTTGAAA[A/G]CAAGAGTGTAGCTAA | 26259 |
rs769274546 | in-del | -/CAGTAGT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933536 | GTTTAATTTGCAACA[-/CAGTAGT]CCAATTGTCCACCAG | 26259 |
rs769286629 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116934861 | TTGTGTGACCACCAC[C/T]GCAGTCAACATGTAG | 26259 |
rs769307613 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946679 | ACCACTAAGACAGGT[C/T]ACGCTGGCCCCACAG | 26259 |
rs769309177 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022149 | ACTTGTTCTTTTTTT[A/G]CAGGGATTGTTGCCC | 26259 |
rs769309626 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021195 | ATTGCATTGTAGTTT[C/T]ACTGTGTAATTTATC | 26259 |
rs769344431 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002841 | ATTCCTGTTTTTTTA[A/G]AGTCTTAGCTCATCT | 26259 |
rs769352388 | in-del | -/GA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001985 | CTACGGACGTGCTGA[-/GA]GAGAGAGATTGGCCG | 26259 |
rs769358473 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116916110 | ATCTACTGTTGATGG[G/T]AATTGTTGCTAGTTT | 26259 |
rs769415782 | snp | C/G | 1.64923e-05 | 0.00287156 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010482 | GGCATTGCCTTGCAG[C/G]CCCATGGCTTCTGCC | 26259 |
rs769470627 | snp | C/T | 1.66236e-05 | 0.00288297 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928041 | GAAATGAATGATGTG[C/T]CTTTCTTTGATATCC | 26259 |
rs769479798 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979120 | AATATTCTGTGCAAG[C/T]ACCATTAGACAGAGG | 26259 |
rs769525503 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116993151 | CTCTGTCGCCCAGGC[G/T]GGATTGCAGTGGTGT | 26259 |
rs769535577 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116958367 | CAAAGAAGCAAAGGA[A/G]CAAGTGAATAGTTCT | 26259 |
rs769562818 | in-del | -/TGTT | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910732 | TAGTTGCTGAATGAA[-/TGTT]TGTTGAATGAAGGAA | 26259 |
rs769598758 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116931535 | ATTTATTTGTATCAT[C/T]CGTTTTCTCCTTAGT | 26259 |
rs769605773 | snp | A/G | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964763 | AGCCCCCTTCCTGGA[A/G]TCAGAGGACGAGGAG | 26259 |
rs769638512 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970979 | TAACAGAAACCAAAA[A/G]AACACACCAGGTATA | 26259 |
rs769662348 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116967160 | ATACTTCTCTGCACC[-/T]TTTTTTTTTTTTTTA | 26259 |
rs769670588 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001831 | CTGTTTGTGTTATGT[A/G]AGCATTAACCAGGTC | 26259 |
rs769694191 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919318 | TGGCTATGGGGCTGG[A/G]CTCTGCAGTCAAGCA | 26259 |
rs769706757 | snp | A/G | | | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032997 | GGGTCCAGCCTTCTC[A/G]TAACAACTGTCCCGC | 26259 |
rs769730050 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025383 | TGAGCATGACAACAT[A/G]GAAGAGCAGAAACAG | 26259 |
rs769757603 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014396 | CTTTAAAGTCGTTGA[A/G]GGTTCCCAAACTAGC | 26259 |
rs769803217 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117005659 | GACAGCAAGGACTGT[C/G]AGCACTGACCAGGGG | 26259 |
rs769820766 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938281 | TTTTAATACCTAATT[A/G]TGGATACAATCCTGA | 26259 |
rs769878895 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116934661 | TTCATAGGAAGTTGC[-/A]AAAAAATAGTACAGA | 26259 |
rs769911978 | in-del | -/G | 5.58436e-05 | 0.00528381 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027524 | GTGGTGGGGCCGGGC[-/G]AGTAAGAGACCATCT | 26259 |
rs769916141 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930284 | TTCCATTCCCACTAA[C/T]AGTGTGCAAGGGTTC | 26259 |
rs769936493 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116957767 | TCCCATAAGGAACTC[A/G]ATCATTACCCGTTAG | 26259 |
rs769945210 | snp | A/G | 1.65531e-05 | 0.00287686 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027476 | GTAATGCGAAACGCC[A/G]ACCTGGACAGCTTCA | 26259 |
rs769952558 | in-del | -/TTG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003485 | CCCCCAAATCAACAT[-/TTG]TGTTTTTGCAGACAG | 26259 |
rs769965847 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962097 | CTGATGATCCCATTG[A/G]TAAAAATAAGGAATT | 26259 |
rs769971010 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116942563 | ATATTTTTAGTCGAG[A/G]TGGGGTTTCACCATG | 26259 |
rs769972429 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918393 | CCAACCCAAACTGGC[C/T]TAAAAACCCAAACTG | 26259 |
rs770060850 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116961196 | AGACGAGGTTTCACC[C/G]TGTTGGCCAGGCTGG | 26259 |
rs770091861 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116940858 | GTGTTATTGAGTCTT[C/G]AGTACCACATTTGAA | 26259 |
rs770104388 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985645 | GAGGTAAGAAGTTAC[A/G]ATTCAAACCTCAGGG | 26259 |
rs770129997 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018543 | ATACCTGTTTCTTCA[C/T]GTGAATCTGAATGGC | 26259 |
rs770142203 | snp | A/G | 1.65119e-05 | 0.00287327 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027434 | AGCAGCCACAGCCTC[A/G]TCACGGCCAACGTGC | 26259 |
rs770239908 | snp | C/T | 6.59207e-05 | 0.00574073 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024188 | GTAACATCGCCCTGT[C/T]GCTCTCCGCCCATCA | 26259 |
rs770273497 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912017 | CGTTAAAAATAATCC[A/C]CTTCAGAAAGTTGGG | 26259 |
rs770281757 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998109 | CAGGTGTGAGCCACC[A/G]CGCCTGGCCCCCAAG | 26259 |
rs770300279 | snp | C/T | 0.000148308 | 0.00861 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010445 | CAGTGGCAACATGGA[C/T]GGGAGGTACGTGAGT | 26259 |
rs770304306 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116945351 | GACATTTGTGTCACT[C/T]CTGCTGTTTTAGGTG | 26259 |
rs770368679 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965026 | AAGTTGGCCAACAAC[C/T]GTCAATGCATTAGTA | 26259 |
rs770383283 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027220 | GGCCTGCTCACCTGA[C/G]CTTCGGGAACTGAGG | 26259 |
rs770409360 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116923343 | GTCCCCAATAGTGGT[A/G]GAGAATCGATATCTG | 26259 |
rs770418460 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009459 | CAACCACATGATCTC[A/C]AGGATAGAAAGTATG | 26259 |
rs770423666 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980941 | TATATGTCACTAAAA[C/T]GTTGGCTCGATCAGT | 26259 |
rs770434205 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954893 | GTCTAACCTCCCTCC[A/T]GCTGGCTCCATCCCA | 26259 |
rs770451075 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116923319 | TTTAATGTGTAATAC[A/G]GGACGAAAGTCCCCA | 26259 |
rs770459115 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980579 | TTTCATTGCTAGGTC[C/T]GCAGTATGATAACAC | 26259 |
rs770466586 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010533 | CTGCTCACACTGCCC[A/G]GTTCTCACTCAACAG | 26259 |
rs770512533 | in-del | -/A | 1.66551e-05 | 0.00288571 | frameshift-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964820 | CTCCTTTGTGAGGAT[-/A]AACAGCTCGTTGGCA | 26259 |
rs770524323 | snp | A/C | 1.68408e-05 | 0.00290175 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024102 | TCATTTGAAGCTTTG[A/C]CTCTAACCCCATTTC | 26259 |
rs770534881 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968155 | TCTAAAAGTGAGTGG[A/G]GTTATTTTGTAATTT | 26259 |
rs770543386 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116934914 | TGTGCTACTCTTTCA[C/G]AGTCTTTGACGGCCA | 26259 |
rs770554370 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022230 | CTGTCTCCTGGGGAT[A/T]CGTTTTGATAATTCT | 26259 |
rs770574781 | snp | A/C | 2.22259e-05 | 0.00333354 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985172 | ATATTAAGTAAATTT[A/C]AAATTGTTACCTGCA | 26259 |
rs770595541 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023381 | TCATCTTTACATTTA[C/T]TAAATGTAATGAATT | 26259 |
rs770615091 | in-del | -/TTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013443 | TTTTCTGAAGGCATA[-/TTT]TGTCTCTTCTCGCTA | 26259 |
rs770664743 | snp | A/G | 0.000270966 | 0.0116366 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911051 | ATATGGACGACTACA[A/G]CCTGGATGAGTTCCG | 26259 |
rs770679139 | snp | A/G | 1.65836e-05 | 0.0028795 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027485 | AACGCCGACCTGGAC[A/G]GCTTCACTACTCACA | 26259 |
rs770689726 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976363 | CTTCAAGCTATTCCC[C/T]ACCTGCACCCTCCCC | 26259 |
rs770730986 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979312 | GGGGCCTGCTGCAAA[C/T]TGGCATGGGTGCCCA | 26259 |
rs770756161 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004055 | GCATGAAGGCAGCTT[A/C]TCCCCTCCTCCGTGC | 26259 |
rs770757930 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017550 | GTAGATAAAGCTATT[-/A]GATTTTGGCATATAA | 26259 |
rs770765275 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960020 | CATTGGGTTCCAAAG[C/G]CTTACTGACAATGTA | 26259 |
rs770770159 | snp | A/G | | | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032557 | AAGCGTGGTTACCTC[A/G]CATCAGATTCTCCAA | 26259 |
rs770790159 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031479 | TGCACTTTGGGAGAC[C/T]GAGGCAGGCGTATCA | 26259 |
rs770804028 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991390 | TGTCATATAACAGCT[C/G]TGTGTGAATTAAGTC | 26259 |
rs770847450 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917785 | ATCACGAGGTCAGGA[A/G]ATCAAGACCATCCTG | 26259 |
rs770858319 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117015542 | GCAACTGGGGATCTC[A/G]CAGGGAGAAGCTTAT | 26259 |
rs770862700 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912389 | GAGACAAGGTCTCCC[C/T]GTATTGCCCAGTCTG | 26259 |
rs770950136 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024559 | TGACATCATTCAGAT[C/T]GCCACAATTCCTACA | 26259 |
rs770956898 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995605 | TGTAAGCTGTATGTA[A/G]GAAGAAGGGCTGCTT | 26259 |
rs770983784 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963697 | TAGATTTCAGTGACT[C/G]AGTGAATCTCAGAGG | 26259 |
rs770992544 | in-del | -/CTT | 1.88834e-05 | 0.00307268 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927997 | TCTAAAAATTATAAA[-/CTT]CTTTCTTTTTTTTTT | 26259 |
rs771027492 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927591 | CTAGTTGAGAGTAGT[G/T]GTGGTTGTCCTGGGA | 26259 |
rs771084903 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936930 | CCTACGTTTAAAAAG[C/G]GACCATTTGGGCTGC | 26259 |
rs771128162 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955845 | TGCAGGGCTAGGTGT[C/T]GTTTGCCATAAGTAG | 26259 |
rs771129093 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962369 | CTTTTTCCCAAGCTT[A/T]GTTGTTTTGCTGTCA | 26259 |
rs771168056 | snp | A/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983770 | ATTAAATATGTTTTA[A/T]AACACAGCAGGAACT | 26259 |
rs771172218 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994846 | ACACTTGGTCCACAT[A/G]AATGTATTTGTAGGA | 26259 |
rs771177312 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919475 | GGAACTTAGCACTGA[A/G]CCTGGAGTACAGTAA | 26259 |
rs771178945 | snp | C/G | 1.64833e-05 | 0.00287078 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949581 | TTCGGGCTGTCCCGA[C/G]AGCAGTCTAAACTGC | 26259 |
rs771217044 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975822 | GGTCATGAAGGACAA[A/G]GAATGACTGAGTAAT | 26259 |
rs771230086 | in-del | -/AAAA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953799 | ACAAAAAAACAAAAC[-/AAAA]CAAACAAACAAAAAA | 26259 |
rs771253289 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116974525 | GGATCCAGCCGATTC[C/T]GAGTGTCTTAATTTT | 26259 |
rs771265600 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116942889 | TTCAAATGATTTTCC[A/T]GCATCAGCCTCCTGA | 26259 |
rs771283042 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117005766 | AGGCGGTTTAACTGC[C/T]TCACTGCCCAGCATC | 26259 |
rs771285128 | snp | C/T | 1.64756e-05 | 0.00287011 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988774 | GCCAGAACCCTCCTT[C/T]ACGCCCACGGCCCGC | 26259 |
rs771305729 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011402 | ACCCCTAGATACCCA[-/C]CCCCCAACTTAGAGC | 26259 |
rs771319858 | in-del | -/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960863 | GTTTCTTCAGATAAA[-/G]GGGCATAGTAGTTGA | 26259 |
rs771336419 | snp | A/T | 3.31631e-05 | 0.00407191 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024334 | GGGTAAGGTGCATTC[A/T]AGACACTCTTGGGAG | 26259 |
rs771338638 | snp | C/T | 3.29506e-05 | 0.00405884 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988758 | CAAAGCCGAAGACTC[C/T]GCCAGAACCCTCCTT | 26259 |
rs771364451 | snp | C/T | 6.59163e-05 | 0.00574054 | synonymous-codon, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985300 | AGCCCTCAGCCAGGA[C/T]GATGCAACCGTGGCC | 26259 |
rs771372819 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018844 | AATTTGTGTTTGCCT[C/T]TGTCTCCTTAACAGC | 26259 |
rs771391888 | in-del | -/TGCCTGACAGGG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026165 | GCCCAGGTCCTCGCC[-/TGCCTGACAGGG]TGCCGTCAGTCCTCC | 26259 |
rs771426709 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000538 | CAGTGGGTCGAGGGT[A/G]GGGCCTGAGAATTTG | 26259 |
rs771445762 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941075 | CAAAAGGGCAAAATC[A/T]GGGCCATAGGTAGAA | 26259 |
rs771499237 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966485 | TTGTGTCTCCAGGGC[C/T]GTGCTGCGGTGGTCG | 26259 |
rs771554969 | snp | C/G | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949677 | AGTTTTGTGTGATGT[C/G]CATTCTCACGATGGT | 26259 |
rs771577915 | in-del | -/GGGAGG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012192 | ATGTACGCACTGCCA[-/GGGAGG]TGTTCCATGCATAGT | 26259 |
rs771607406 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913447 | CTTATAGATAAGTCA[A/G]TTAACACATATTTTG | 26259 |
rs771652159 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982225 | GATTTAAACACCCCA[A/G]TTAAAAGCAAGACCA | 26259 |
rs771661251 | snp | C/T | 3.29658e-05 | 0.00405978 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024180 | CCGCAGTGGTAACAT[C/T]GCCCTGTCGCTCTCC | 26259 |
rs771661255 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956969 | TGAGACTCCATCTCC[A/C]AAAAATAAACAAAGT | 26259 |
rs771672574 | in-del | -/GATGGTCTC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912676 | CACTGTGTTAGCCAG[-/GATGGTCTC]GATCTCCTGACCTCG | 26259 |
rs771676817 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969317 | CTGAGCTTGTTTCAT[G/T]GGTCTGATTCGGGTT | 26259 |
rs771696815 | snp | C/G | 3.34526e-05 | 0.00408965 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928016 | TTTCTTTTTTTTTTC[C/G]CCTCAGAATGAAATG | 26259 |
rs771702411 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965567 | CCACAAGCTTCATGT[-/C]CCCACTTGCCCAAAA | 26259 |
rs771714228 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956013 | TTTGCAATAAACTCT[C/T]TCCTCATTGTTACTT | 26259 |
rs771745608 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936815 | AGGAGGAGAGGACTC[A/C]GGATGTGATAAGCGT | 26259 |
rs771766438 | in-del | -/TCTG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964299 | CCTGCAGCATCTCTC[-/TCTG]TCTTTCCTGTGAGTG | 26259 |
rs771785221 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023990 | GGTCCTCCCTGACAG[C/T]CTGTGCTTGATGTCC | 26259 |
rs771800519 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935973 | GAGGTACTGTTCTAT[A/G]TAGTGAAGACAGCTG | 26259 |
rs771851435 | snp | G/T | | | missense, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024306 | GAACCAGAAGCTGTG[G/T]GAGGTGTATTCCGGG | 26259 |
rs771882784 | snp | A/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909865 | AAGATTAAGTGAAAT[A/G]TGAGTTGAGATATGA | 26259 |
rs771906729 | snp | A/C | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028067 | TGAGTTTGCGGTGGA[A/C]CAGCTGGCCTTCCAG | 26259 |
rs771939322 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023657 | CTTTCCCTTTCTCAG[C/T]TCCAGCAAGACAGCA | 26259 |
rs771949025 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919164 | GGACGACTGTGTTTT[C/T]TGTTCATCCAACATA | 26259 |
rs771964153 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936334 | GGGTGGTTGTCGTAC[A/G]CTGAATAATGGCCCT | 26259 |
rs771973251 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116911998 | AAGCTGGGGACCCTG[C/T]GTCCGTTAAAAATAA | 26259 |
rs771987393 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939316 | TCTGAAATCCAAAAT[A/G]CTCCTGGTTTTAAGC | 26259 |
rs771993862 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116961131 | CTCCCAAGTAGGTGG[G/T]ATTACAGGCACGCAC | 26259 |
rs772032889 | snp | C/T | 0.000272517 | 0.0116698 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911062 | TACAGCCTGGATGAG[C/T]TCCGTCGGCGCTGGC | 26259 |
rs772039069 | in-del | -/AA | 5.59433e-05 | 0.00528853 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964887 | TCCTCCCTATTAAGG[-/AA]AAAAAAAAGCTTTAC | 26259 |
rs772082701 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980089 | TTGGGACTCAAACTT[C/T]GTTGCATTCTTGGAG | 26259 |
rs772111792 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951923 | TTTTCCAGTGGGGAA[A/T]CATTCTTTCCAAAGC | 26259 |
rs772121005 | snp | G/T | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985258 | CCCTGTTCATCGTTT[G/T]GAGCACGATGCAAGA | 26259 |
rs772167825 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918042 | TCCTCCCAAGCCTCA[C/T]GTTTTATGAAGCTTT | 26259 |
rs772181283 | snp | G/T | 1.64814e-05 | 0.00287061 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949589 | GTCCCGAGAGCAGTC[G/T]AAACTGCATCCCCCT | 26259 |
rs772250391 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025441 | TTTGTTCCCCACTTA[A/C]CGCAAATCAAGGTAA | 26259 |
rs772260854 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920622 | TTTCATGGAGAACCT[A/G]AAGGAGGTGAGGAGT | 26259 |
rs772261673 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938503 | CTGTTGTACAAATTT[A/C]AGATTGTGTTATTTA | 26259 |
rs772285785 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023045 | GTAGTTCACTTTGAG[-/T]CCTTTTCTGTTAAAG | 26259 |
rs772287525 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007598 | GCAGAATATTTTCTC[C/T]GGGATTTGTGCTGGG | 26259 |
rs772329422 | snp | A/C | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984538 | TGAGGAAGGATGTGA[A/C]ATTCAGGCTGAGCAT | 26259 |
rs772337307 | snp | A/G | 1.64999e-05 | 0.00287222 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010296 | TGTGTGGAATTGTGG[A/G]CCCACACATTTCTCT | 26259 |
rs772355744 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008982 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 26259 |
rs772361798 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921548 | AATGACTTACCTCTA[C/T]AAAAGATTTTAGCTC | 26259 |
rs772378215 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116931852 | TTTATTTCTTTCTGT[A/T]GCCTAATTGCTGTGA | 26259 |
rs772381775 | snp | A/G | 1.64944e-05 | 0.00287175 | stop-gained, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985368 | ATGAGGAGGGGTACT[A/G]GCAGATAGCTGCGGA | 26259 |
rs772389391 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116989968 | GCTCCCGACCTGTTA[C/G]CTCCTGAACCTCCCG | 26259 |
rs772422338 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996711 | TGTAGACAGATAACT[C/T]GTGGAGACCAGTTTT | 26259 |
rs772434070 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020068 | CACAGCCTAAATGCA[C/T]GTCCCCCAGCACACA | 26259 |
rs772445097 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116942289 | GCCTCCAAAGGTGCT[A/G]GGATTACAGACTCTT | 26259 |
rs772462895 | snp | C/T | 1.66499e-05 | 0.00288525 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024353 | CACTCTTGGGAGTTC[C/T]TAGTAGGAACAGGGA | 26259 |
rs772466610 | snp | C/T | 1.65255e-05 | 0.00287445 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988639 | ATGAATTTATGGGAC[C/T]AAACAACTCTTACCT | 26259 |
rs772468595 | snp | A/G | 9.95438e-05 | 0.00705422 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928138 | CACAGGTAAGGTGTC[A/G]CCAACAGATGTTCCA | 26259 |
rs772482534 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962772 | CCCCCAGTCTAGACA[G/T]TCAAACATGTCTCAT | 26259 |
rs772499573 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939552 | TCCATGTAATTAAAG[A/C]ATGGCTACATTTATA | 26259 |
rs772500491 | snp | A/C | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975980 | TAAATATGTTGCATC[A/C]GCGTTAATTTCCTGG | 26259 |
rs772519177 | in-del | -/AAAT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929581 | TTTTTTTAAATGGAC[-/AAAT]AAAGTTATATATATG | 26259 |
rs772552087 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965312 | TCCTGTCACTTAATA[C/T]ACCATACCAGATAAT | 26259 |
rs772617658 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116934888 | GTAGAACATTCATCA[C/T]GAGAATCTCTTGTGC | 26259 |
rs772621748 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022171 | TTGTTGCCCCTTGCT[A/G]GCTTCCTCAGGCTGC | 26259 |
rs772639446 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953616 | TCCACTAAAAAATAC[-/A]AAAAAAATTATCCGG | 26259 |
rs772641965 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996961 | ACGAGGTCATAACAA[C/G]ACCTTCGTGATGAAC | 26259 |
rs772659476 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988806 | TGTCACATGTCTAGA[C/T]GTCTCGGCCAACCAA | 26259 |
rs772677072 | snp | A/T | 1.66228e-05 | 0.0028829 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928045 | TGAATGATGTGCCTT[A/T]CTTTGATATCCAACT | 26259 |
rs772678082 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990206 | ATGTGTGGCATCCTA[A/T]CATCTCAATGTGAAA | 26259 |
rs772679512 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944579 | AATGCTGTGCAGACC[A/G]GGATCACGCTGATCT | 26259 |
rs772723229 | in-del | -/TTT | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976451 | GTTTCCAAAGGATCC[-/TTT]TTTTTTTTTTTTTTT | 26259 |
rs772729712 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009393 | CAAGACCCTGTTCCC[C/T]CACCCCCTCAAAAAA | 26259 |
rs772743885 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013439 | AGTTTTTCTGAAGGC[-/T]ATATTTTGTCTCTTC | 26259 |
rs772764093 | snp | A/G | 4.94319e-05 | 0.00497127 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010340 | CCTGGTGTATAGCCT[A/G]GAAGCAGGACGCCGC | 26259 |
rs772788672 | snp | A/T | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985354 | GATGTTATCCCCCAA[A/T]GAGGAGGGGTACTGG | 26259 |
rs772796877 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012212 | GTGTTCCATGCATAG[C/T]GTCAAAGGGCTCTCT | 26259 |
rs772837485 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968137 | ACAATGTTAATTTTT[-/T]AATCTAAAAGTGAGT | 26259 |
rs772850772 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116949133 | TCTCATCTCCTTTTC[C/T]TCATCCTGATCTTTA | 26259 |
rs772851629 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933408 | TTCTCATCCAAAGAG[C/T]TTATCAGAGAAAGAT | 26259 |
rs772891707 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029923 | GCCCAAAAGCAGTTT[A/G]AAAAAAAAAAAGACA | 26259 |
rs772904992 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002071 | TCCTTTCAGGCTTAG[C/G]TCACAATAGGTGTTG | 26259 |
rs772944537 | snp | C/G | 1.65861e-05 | 0.00287972 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928110 | CTGGACAGGAAAGAA[C/G]TAGGAAGATGTGCAC | 26259 |
rs772954599 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010396 | GTGACTTCACGTGTG[C/T]CAACCTCAGCGACAG | 26259 |
rs772957806 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116958647 | GTTAGGGTTGGGGAG[C/G]AGCACGGTGCCATAA | 26259 |
rs772958875 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021293 | TTTTCTTATCTTTTC[C/T]GTCGATTTAATAATG | 26259 |
rs772972029 | snp | A/G | 1.64893e-05 | 0.0028713 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964769 | CTTCCTGGAATCAGA[A/G]GACGAGGAGGATGAG | 26259 |
rs772972369 | snp | A/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979150 | GTCTTAAGGATTGTC[A/G]ACATTATTTCACAGT | 26259 |
rs772984121 | in-del | -/TC | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030926 | CTTTCACAAACAAGT[-/TC]TGAGTTTTTAGCCAA | 26259 |
rs773003306 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971021 | AGATAGGGTATGTTC[A/G]TAAATGTAAACTTTT | 26259 |
rs773058092 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991302 | ATTTTTACAGAGACA[A/G]GACTTTCCATCTGAT | 26259 |
rs773060304 | snp | C/T | | | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977593 | ATTCCCCACTCCCCT[C/T]CTTAGAGGCATCTGC | 26259 |
rs773076733 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990243 | CATCTCACTGTGAAA[A/C]GGCCTCCCCTTGTGC | 26259 |
rs773195683 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116993380 | GTGCTGGGATTACAG[A/G]TGTGGGCCACCGCAC | 26259 |
rs773251146 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000887 | GAAAGACATTGTGAT[A/G]TGGTCACAAAGTGGC | 26259 |
rs773270176 | in-del | -/AGTT | 3.32474e-05 | 0.00407708 | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028184 | TTAGGGATGTGCCTC[-/AGTT]GGGAGCAAGGAGAAA | 26259 |
rs773270676 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969705 | GCCCTCGCTGGTCTA[C/T]ACGCACATTCTCGGT | 26259 |
rs773281456 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926823 | TTTTTATGCTCTGGG[C/G]TGTCTTTTAGCCCCG | 26259 |
rs773283188 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994598 | ATATGTGGTCTCAAC[C/G]CCACTTTAAACAATG | 26259 |
rs773288853 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919353 | TGAGTTCAGATTCTG[A/G]CTCTGCTGTTACCAG | 26259 |
rs773289516 | in-del | -/AG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026173 | CCTCGCCTGCCTGAC[-/AG]GGTGCCGTCAGTCCT | 26259 |
rs773334421 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938310 | GATCCCTTTTTGGAA[A/G]CAATTCTCACCTCTG | 26259 |
rs773353469 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004676 | CTCTGCACCAATAGA[C/T]ACTTTCCCCATCTTG | 26259 |
rs773376123 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116974140 | GCCCCAGTGAGGGCT[C/T]AGGGAAGCCAAGGTG | 26259 |
rs773390076 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116949387 | GGCAATGTCTCACAC[A/G]TCCTGTGTCCTCGAG | 26259 |
rs773392499 | snp | G/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987276 | TTTGGCATATGGTCA[G/T]GGCAGCGCTGTCCTT | 26259 |
rs773403377 | snp | A/G | 1.64928e-05 | 0.00287161 | missense, synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945508 | CGAGCCAAGGAACAC[A/G]TGTTACGAACCAACT | 26259 |
rs773415921 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116930351 | TTTTTGGTAATAGCC[A/G]TTCTAACAGGTGTAG | 26259 |
rs773422393 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117015730 | ACCAATTTAAATTGT[A/G]CAATTCAGTGTTTTA | 26259 |
rs773431344 | snp | A/G | 3.29603e-05 | 0.00405944 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024189 | TAACATCGCCCTGTC[A/G]CTCTCCGCCCATCAG | 26259 |
rs773468832 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929097 | AGGCATGAGCCACCG[C/T]GCCCGGCCCCATTGA | 26259 |
rs773478118 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117005631 | CTTGTCGAAACACCA[C/T]GTGATGCGTGCAGAC | 26259 |
rs773598560 | snp | C/G/T | 0.000148989 | 0.00862984 | missense, synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027478 | AATGCGAAACGCCGA[C/G/T]CTGGACAGCTTCACT | 26259 |
rs773617564 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003599 | TCTGTCTCCCAAAAG[C/T]GCATTCTTTAGAAGT | 26259 |
rs773618547 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018781 | CCATCCATGCTGGTA[C/T]CTAAATACAATAGGA | 26259 |
rs773648719 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939493 | TCCTTTTCTAAGGAA[C/G]TTATTAACACCTGGA | 26259 |
rs773657749 | in-del | -/GCT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913619 | CTTCATGCTGGGTAG[-/GCT]GCTGCTGCTGCTACG | 26259 |
rs773660244 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964009 | AGTCTGAGTAGGTTC[A/G]GCCTGGCCTGGCTTT | 26259 |
rs773661783 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915738 | GCTCACTGCAACCCT[G/T]ACTTCCCGGGTTCAA | 26259 |
rs773668776 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023169 | AAATTGACGTGTGTG[C/T]GCATGCTTGCATAAC | 26259 |
rs773670137 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116942435 | GCTGGAGTGCAATGG[C/T]GTGATCTTGGCTCAC | 26259 |
rs773708762 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017505 | TGCCGTTTAAAATGA[A/G]TCTTTCACCAAAGGC | 26259 |
rs773709630 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954385 | CATTACTTTCTTTGA[C/T]TTGTTGCAAAAACAC | 26259 |
rs773721749 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012007 | TTTTTAATGGAGGAT[G/T]TGTGTAGGTTATATG | 26259 |
rs773723391 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027864 | CCCACGTTGACCGCT[A/C]AGCCGGGGACTGTGA | 26259 |
rs773725289 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027821 | CCTTGCCCTGTGACA[C/G]TCACTGCGCCCATCG | 26259 |
rs773736265 | snp | C/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985802 | TGGTGTTATCCCAGT[C/G]CATCTGGGAAGGAAG | 26259 |
rs773754172 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011581 | GCCCCACATGTGGCA[C/T]GGCAAAAGAATCAAG | 26259 |
rs773760980 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016868 | TATCCAGCTATCCTG[A/G]CACCATCTGTTGAAA | 26259 |
rs773766361 | in-del | -/TTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912452 | AATTGAGAATCATTC[-/TTT]TTTTTTTTTTTTTTT | 26259 |
rs773784093 | snp | C/G | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986005 | CATTGGTACAGGAAC[C/G]TCTAGATTTGTAGAG | 26259 |
rs773786942 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031955 | AATTTTTGGTGACTC[-/T]TGAGTGCTGGCAGTT | 26259 |
rs773800235 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925119 | AAAATAGATTCTGAA[A/G]TGGAGATTTGCATGT | 26259 |
rs773819006 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027021 | ATAGATGATGGAGAG[C/G]CTGGCTGGGAAAGCT | 26259 |
rs773845919 | snp | A/C | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909680 | AACCATTTATTGAGC[A/C]TGTATTAATCACCAG | 26259 |
rs773928199 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116948289 | CAAGAGATTTTCTGT[G/T]ATTGTAACCTTGGTT | 26259 |
rs773936548 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998274 | AGGGCTGGCACCAAG[C/T]CTTAAATGTCTTTTG | 26259 |
rs773944189 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946115 | TAAAGCTGTTTGAGG[C/T]ATGACGAGACAGCAG | 26259 |
rs773960452 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979325 | AACTGGCATGGGTGC[C/T]CATCCACAGCTGCTG | 26259 |
rs773973399 | in-del | -/CTTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116934955 | AGTCCTTCCCCGACC[-/CTTT]CTTTCACCCCCAGCT | 26259 |
rs773986498 | snp | C/G | 1.68371e-05 | 0.00290143 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024105 | TTTGAAGCTTTGACT[C/G]TAACCCCATTTCCCT | 26259 |
rs773988379 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935935 | TCATTTGGTTATTTA[C/T]ATAGAGCTGACTATG | 26259 |
rs774050307 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116923475 | TAGAATAAATTTGGC[C/G]AGTCTCACATTGCTG | 26259 |
rs774050389 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991422 | TGTCATGGGTAACTC[C/T]GTGAGATTTTAGTAT | 26259 |
rs774091105 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010660 | GCTTCATTTCTGAAG[C/T]ACCACGGGAAGGTTT | 26259 |
rs774093429 | snp | A/G | 3.29859e-05 | 0.00406102 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964773 | CTGGAATCAGAGGAC[A/G]AGGAGGATGAGCCTG | 26259 |
rs774125361 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966818 | CTCCCGGGTTCAAGT[A/G]ATTCTCCTTCCTGCC | 26259 |
rs774165583 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933662 | TCTTAAACAGAACCC[C/T]GTTAGCGTACAGTGA | 26259 |
rs774166467 | snp | A/T | 1.90962e-05 | 0.00308994 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911054 | TGGACGACTACAGCC[A/T]GGATGAGTTCCGTCG | 26259 |
rs774188489 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010416 | CTCAGCGACAGCCCT[C/T]CCAACCTCATGGTCA | 26259 |
rs774193211 | snp | A/G | 4.98567e-05 | 0.00499258 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027491 | GACCTGGACAGCTTC[A/G]CTACTCACAGGAGGT | 26259 |
rs774215217 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965693 | GGAACAAAACTAAAG[C/T]AGCTAATGGGGAATT | 26259 |
rs774231885 | in-del | -/AACT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944329 | ATCTGCCATCCTGCA[-/AACT]AACTCTCTGTCAGTG | 26259 |
rs774274860 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022232 | GTCTCCTGGGGATTC[A/G]TTTTGATAATTCTTA | 26259 |
rs774291259 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021418 | TCTGATTGTTCCCCC[C/G]AATAGGAAAAAGTTA | 26259 |
rs774306293 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915671 | TTTTTTTTTTTTTGG[A/G]AGATAGAGTCTTACC | 26259 |
rs774324972 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003063 | TTAAAAAGGAGCATC[A/C]CTAGTCTTGTATGTG | 26259 |
rs774328529 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116974440 | CATGTTTTAGTAATG[C/G]GGCTAATTCAGCCCT | 26259 |
rs774365843 | in-del | -/GAG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021054 | CCAAGTCACTCCCCA[-/GAG]AAGGATTTCTGCTCG | 26259 |
rs774369103 | in-del | -/TTCT | 0.000225035 | 0.010605 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927998 | CTAAAAATTATAAAC[-/TTCT]TTCTTTTTTTTTTCC | 26259 |
rs774379250 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030727 | ATTCGTGGAAGTCGC[C/G]TGGGTTTTGTAAAGG | 26259 |
rs774418150 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116916476 | GGGGTCAGGGTAATA[A/G]CCACTGCCCCCATTA | 26259 |
rs774429315 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024639 | CTATTCTGATTATTT[C/T]AGGATTTCTCCATCT | 26259 |
rs774473163 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116915386 | TGTTTTCCCACTTTT[A/C]AAAGTTTTTAAGCTC | 26259 |
rs774487171 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994909 | GGGACATGTGCCTCC[A/T]TGATTTTGATAGACA | 26259 |
rs774520966 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951038 | GCCAATTATGAATTT[C/T]TTCTCTGGAGCTCCC | 26259 |
rs774545305 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920618 | CACATTTCATGGAGA[A/G]CCTAAAGGAGGTGAG | 26259 |
rs774568782 | snp | A/G | 4.94352e-05 | 0.00497143 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985301 | GCCCTCAGCCAGGAC[A/G]ATGCAACCGTGGCCA | 26259 |
rs774578340 | snp | A/T | 1.64754e-05 | 0.00287009 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988775 | CCAGAACCCTCCTTT[A/T]CGCCCACGGCCCGCC | 26259 |
rs774600432 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919527 | GTGCCATTATCGTTA[A/G]TACTCAGAGTTTGCT | 26259 |
rs774605794 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995635 | TGATGGTTTTTTACT[G/T]TTGGACAAAAATGAA | 26259 |
rs774630309 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002562 | AAGTCACCTTTGGGA[-/T]GGTGGTGAAAGTCAT | 26259 |
rs774649516 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975897 | TATGTGGAATTCTGG[A/G]TTGGATCCTGGACCA | 26259 |
rs774699272 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116949563 | AAAGCACGATGCTTG[A/G]CTTTCGGGCTGTCCC | 26259 |
rs774737338 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020335 | GTTTCCCCATTTTTT[A/T]AATTATACTCTTAGA | 26259 |
rs774749274 | snp | A/G | 6.66134e-05 | 0.00577081 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945521 | ACATGTTACGAACCA[A/G]CTGGAAGGTGGGCAG | 26259 |
rs774780381 | snp | A/G | 1.64789e-05 | 0.0028704 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024196 | GCCCTGTCGCTCTCC[A/G]CCCATCAGCTCAGGG | 26259 |
rs774809146 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116974613 | AATGTAAAATTCACA[A/G]TGTCTGTCATCCAAT | 26259 |
rs774812881 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988763 | CCGAAGACTCCGCCA[A/G]AACCCTCCTTTACGC | 26259 |
rs774828714 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937462 | AGGAGTTCCCTGCCA[A/G]GCAGGAAGAAAACCC | 26259 |
rs774846641 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019063 | ATACTTTTTCTCTTC[C/T]CTTACCTACGCATGC | 26259 |
rs774889886 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000676 | AGGTTTGAATCCTGG[G/T]GCCAAAACTTCCTAA | 26259 |
rs774900892 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987530 | CATGCGTGTTTGTAG[A/G]GCCTTCCTTACCCTC | 26259 |
rs774930316 | snp | A/G | 0.00027697 | 0.0117647 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911066 | GCCTGGATGAGTTCC[A/G]TCGGCGCTGGCAGGA | 26259 |
rs774964033 | in-del | -/TT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912453 | ATTGAGAATCATTCT[-/TT]TTTTTTTTTTTTTTT | 26259 |
rs774964294 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029451 | GCACAGAATACAAAA[C/T]CCAGGGGATGGGGCT | 26259 |
rs774994719 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913529 | GAAAGTGTCATTAAG[A/G]AAATTATAAGAGAAA | 26259 |
rs775018540 | in-del | -/CTGT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026100 | GCCCCAGTCTGGCTG[-/CTGT]TTGTTTGGTCACTGT | 26259 |
rs775116891 | snp | C/G | 1.77972e-05 | 0.002983 | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985194 | TTACCTGCATTGTTT[C/G]TTGCTGCATAGGGTT | 26259 |
rs775117651 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925776 | CATTAACAGTGAGAC[C/T]AGCATGAGGTCTCAT | 26259 |
rs775132881 | in-del | -/T | 1.64789e-05 | 0.0028704 | frameshift-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985346 | GATGTCGTGATGTTA[-/T]CCCCCAATGAGGAGG | 26259 |
rs775152672 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956016 | GCAATAAACTCTCTC[C/T]TCATTGTTACTTGAG | 26259 |
rs775173703 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935979 | CTGTTCTATATAGTG[A/T]AGACAGCTGAGAATA | 26259 |
rs775211840 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968272 | TGTCTGCTCCATTCT[G/T]AAGTAACCATATTTT | 26259 |
rs775215794 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982251 | GACCAACTACATGCT[A/G]TCTATGGAAAACCCA | 26259 |
rs775228805 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116949258 | CTTTTTCACATACTT[C/T]ATAAGTTTCTTTAGA | 26259 |
rs775229256 | snp | C/T | 1.67478e-05 | 0.00289372 | intron-variant | FBXW8 | GRCh38.p7 | 12:117024119 | TCTAACCCCATTTCC[C/T]TTCTCTGCTCTTCCT | 26259 |
rs775236710 | snp | C/T | 1.64827e-05 | 0.00287073 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024182 | GCAGTGGTAACATCG[C/T]CCTGTCGCTCTCCGC | 26259 |
rs775249436 | snp | A/G | | | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032816 | CTTTCTGAAAGGAAA[A/G]GCTGACACCCCCAAG | 26259 |
rs775259615 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981207 | GATATAACTGTAGTA[A/G]CTGATAAATTGACCA | 26259 |
rs775296302 | in-del | -/CTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116964518 | AAGCGTGTTCACAGC[-/CTT]CTGTCATCTAGTTGA | 26259 |
rs775343346 | snp | C/G | 1.65518e-05 | 0.00287674 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988869 | GTACGAAGGAAGCAA[C/G]GTACACAACTAGCAA | 26259 |
rs775359124 | snp | G/T | 1.74248e-05 | 0.00295163 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027512 | CACAGGAGGTTAGTG[G/T]TGGGGCCGGGCGAGT | 26259 |
rs775402100 | in-del | -/GTGAT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001328 | GGGCTATTTGTTTCA[-/GTGAT]CTGATTTTAGCTGCC | 26259 |
rs775409479 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116971412 | TTGGTGTTTAAGAAA[C/T]CCTTTTTAGGGCGTT | 26259 |
rs775417832 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011788 | CATTTATATCTTCAG[C/T]CACAGTTAGGCTCAC | 26259 |
rs775427815 | snp | C/G | 1.64822e-05 | 0.00287068 | missense, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024286 | TCCGTGTGGGATTAT[C/G]GGATGAACCAGAAGC | 26259 |
rs775431511 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935145 | AAAACGTGCATAAAC[A/C]AAGTAATAAAGAAAA | 26259 |
rs775437631 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013702 | TAAAAGTTACACAAA[C/G]TAATGATGCTTCTTG | 26259 |
rs775461470 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116993278 | CTGGCTAATTTTTGT[A/G]TTTTTAGTAGAGACG | 26259 |
rs775498143 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987895 | GCGAGTCAAGCGCAT[-/TG]TGTACTTTCTCCACC | 26259 |
rs775511486 | snp | C/T | 1.64925e-05 | 0.00287158 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010308 | TGGGCCCACACATTT[C/T]TCTTCCTCTCTCAGA | 26259 |
rs775524326 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022426 | TTAGGAGGCTGAGGT[G/T]GGTAGATCCCTTGGC | 26259 |
rs775537485 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116918065 | GAAGCTTTTAGTAAT[A/G]GCACTTAGCAGCCAT | 26259 |
rs775559370 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014635 | TGGTTAGGTTCAGAC[A/G]GCAAGTTCTGTTTAC | 26259 |
rs775560026 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947935 | CGCTCAGTGCTCAGG[C/T]GAGGTTGGCTGTAGG | 26259 |
rs775563563 | snp | G/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116910466 | CACCATATGTATATA[G/T]CAGTTTCTTTATCCA | 26259 |
rs775575923 | in-del | -/AT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021241 | TTAAACATCTTACAC[-/AT]GTTTAAAAGCCATTA | 26259 |
rs775599245 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116949691 | TGCATTCTCACGATG[A/G]TGTGGTCATTGCGGG | 26259 |
rs775629233 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020074 | CTAAATGCATGTCCC[C/T]CAGCACACACCTGTG | 26259 |
rs775634307 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951177 | CCACGTTCTGTGGAT[C/T]GATAGGATGAAACTT | 26259 |
rs775648132 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117026775 | GGCATCCACCTGGAT[A/G]AGACATCTTTTTAAT | 26259 |
rs775666263 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116939332 | CTCCTGGTTTTAAGC[A/T]TTTTGGATAAGGGAT | 26259 |
rs775717341 | snp | A/T | 1.64806e-05 | 0.00287054 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949592 | CCGAGAGCAGTCTAA[A/T]CTGCATCCCCCTTTT | 26259 |
rs775790629 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963799 | TTAAAATCATTGGCC[A/T]ATCTTTGTGATTGTG | 26259 |
rs775811031 | snp | A/C | 1.65921e-05 | 0.00288024 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928139 | ACAGGTAAGGTGTCA[A/C]CAACAGATGTTCCAG | 26259 |
rs775811121 | snp | A/G | 1.65231e-05 | 0.00287424 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988641 | GAATTTATGGGACTA[A/G]ACAACTCTTACCTTT | 26259 |
rs775819417 | in-del | -/T | 0.476384 | 0.106067 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928005 | TTATAAACTTCTTTC[-/T]TTTTTTTTTCCCCTC | 26259 |
rs775843497 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924751 | GATGTGGCTTCATAT[C/T]CTTGTCAGATCATGC | 26259 |
rs775852250 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116934726 | TTGGTAATATCCCGC[A/G]TAACTACAGAACAGT | 26259 |
rs775858836 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919597 | TAAGCCCTTAGCTTC[C/T]GCCTCTTGTGAATCC | 26259 |
rs775893256 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950550 | ATCTTTCTTTAAGCA[A/G]CATTCCTTAAAGAGC | 26259 |
rs775900783 | snp | A/G | 3.30387e-05 | 0.00406427 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945384 | CAAGACGTGGAAGGT[A/G]ATTGCAGAGGATGAG | 26259 |
rs775916512 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996739 | TTTCTGGGCTGTTGA[A/G]TGATGCTGACTCCCA | 26259 |
rs775924252 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116923436 | TTGAAGGAATACTAA[C/T]ATTTTGAATTTATTG | 26259 |
rs775948543 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007657 | TCTGAGAATGAGTCA[A/G]GTGGTCATGGGTTGA | 26259 |
rs775951089 | snp | C/G | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977438 | GATAGCCTTTCAAAT[C/G]GTTATTCTTAAAAAT | 26259 |
rs775953918 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962782 | AGACATTCAAACATG[G/T]CTCATCTGTTGTGTC | 26259 |
rs775962069 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116933678 | TTAGCGTACAGTGAC[-/T]TAAGTTAGCTGTGAT | 26259 |
rs776006100 | in-del | -/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116982625 | GATGGAGCCCTGGAT[-/T]TTTTTTTTTTTTTTT | 26259 |
rs776011595 | snp | A/C | 1.66493e-05 | 0.0028852 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024355 | CTCTTGGGAGTTCCT[A/C]GTAGGAACAGGGAAG | 26259 |
rs776017479 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917223 | AACTAATAAAAATTA[A/G]TAAGATTTTAGGTGC | 26259 |
rs776018688 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030495 | AATGCGTCTGGACCA[C/G]TGGGGAAAATATTTT | 26259 |
rs776018786 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983918 | TACAGAAAGGCTAAC[A/G]GGCTCAGAGCTGTTA | 26259 |
rs776066709 | in-del | -/TCTC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001629 | TAGATATTATAACCT[-/TCTC]TCTCTTGGTGATTAT | 26259 |
rs776103543 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020191 | AAGAGCTAGTTAATC[A/G]TGTCACCTACGTCAT | 26259 |
rs776136208 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992833 | TCATTGGTTGATGGC[A/C]CTTAGGTTGGTTTCT | 26259 |
rs776137423 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116931890 | TTCTAGTACTATGTT[A/G]AATGGAAATGGTGAG | 26259 |
rs776154454 | in-del | -/T/TT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965924 | CACCATGCCCAGCTA[-/T/TT]ATTTTTTTTTTTTTT | 26259 |
rs776175090 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116940232 | CAGAGCTAGAGCCCT[A/G]TCTTTAGCACCATCC | 26259 |
rs776191413 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944584 | TGTGCAGACCGGGAT[A/C]ACGCTGATCTGCTCG | 26259 |
rs776196104 | in-del | -/TTTATT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990652 | ACTTATCTGAATGGA[-/TTTATT]CCTGTAGTAATACAG | 26259 |
rs776249484 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116914999 | TTTAGAGACATTATC[A/G]TCTTCATTTCTCCCA | 26259 |
rs776274395 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013449 | GAAGGCATATTTTGT[C/T]TCTTCTCGCTAAGAC | 26259 |
rs776310090 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029755 | GCTGGGATTACAGGC[A/G]TCCGCTACCACAACT | 26259 |
rs776311370 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926011 | GGTGATGCCAAGATA[C/T]GGGCATTGTCTTCCA | 26259 |
rs776361420 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936869 | GTTTTGTGAATAAGA[C/T]GGGAAGCCTTTGGAG | 26259 |
rs776364555 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969426 | TTTAACAGATCGACA[C/T]TATGATATTTACACT | 26259 |
rs776364760 | snp | C/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985298 | CTAGCCCTCAGCCAG[C/G]ACGATGCAACCGTGG | 26259 |
rs776406255 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116949555 | TAGGTGAAAAAGCAC[A/G]ATGCTTGGCTTTCGG | 26259 |
rs776428871 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973144 | ATTGAATAAAATAGG[A/C]ATATATGAGTATATC | 26259 |
rs776443595 | snp | C/G | 0.000236798 | 0.0108786 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911113 | CAGGCGCCGAAGAAG[C/G]GGCGACGGCCCGAGG | 26259 |
rs776459805 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966192 | TTCTGTGGTATAATT[-/A]ATATTTCATATGTTT | 26259 |
rs776473331 | snp | C/T | 1.64972e-05 | 0.00287199 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964664 | CCTGCTCTTCAATCT[C/T]CTTTTGGAACCAAGT | 26259 |
rs776476359 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116989196 | TATACATAGTGTTCT[A/G]TACCCAACATTTTTA | 26259 |
rs776482029 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001788 | TATCATCTCTTCGCT[A/G]GACTCACTGCTCTGA | 26259 |
rs776492425 | snp | A/G | 1.71973e-05 | 0.0029323 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988893 | CTAGCAAGATATATA[A/G]TTAACAAAAAAGAAT | 26259 |
rs776498484 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000753 | AAAGGGAGTAAAATC[A/G]TGGTACCTATCTTAC | 26259 |
rs776513131 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116934162 | GCTTTGACTTTGCCT[-/C]CTTTCCATATCCCCT | 26259 |
rs776521385 | in-del | -/TT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927220 | TCACACTCATATTTC[-/TT]TGTGCTACCAGGATC | 26259 |
rs776523289 | in-del | -/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953086 | AATATTTTGTTAAAT[-/G]TATACTGTTTTATAT | 26259 |
rs776561341 | snp | C/G | 1.66418e-05 | 0.00288455 | missense, intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985394 | GCGGAATTTGAAGTT[C/G]CGAAACTGGTGAGCT | 26259 |
rs776577161 | snp | C/T | 3.29739e-05 | 0.00406028 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010318 | CATTTCTCTTCCTCT[C/T]TCAGATCCTGGTGTA | 26259 |
rs776595850 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116916683 | CAGGAGGATCACCTT[A/G]GCCCAGGAGTTTGAG | 26259 |
rs776709948 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117003185 | TTTGTATGCGTGAAG[C/G]CTGTCTTTACTGTAA | 26259 |
rs776714625 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116927804 | AGTGAATATAAGGAG[G/T]GAAGGCGTGTGGGGG | 26259 |
rs776749333 | in-del | -/CA | 1.65233e-05 | 0.00287426 | frameshift-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027425 | ATCTCATTCAGCAGC[-/CA]CAGCCTCATCACGGC | 26259 |
rs776755109 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117015924 | TCTCCTATAAATGAA[A/G]TGATGTAATCTATGA | 26259 |
rs776764090 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950385 | GACTGTATACTTAAT[A/G]CCATAAAGTAGAAAG | 26259 |
rs776781703 | snp | A/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983771 | TTAAATATGTTTTAT[A/T]ACACAGCAGGAACTA | 26259 |
rs776784141 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985556 | CTTACAAAATAGGTA[A/G]TAGCATTTTCCCCAT | 26259 |
rs776793014 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116929008 | TAGAGATGGGATTTC[A/G]CTGGCCAGCCTGGTC | 26259 |
rs776799186 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117017325 | AGAAAGGTTCAGTGA[C/T]CAGTCAGTCCGAAGG | 26259 |
rs776802162 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998003 | ATATTTTTTAGTAGA[G/T]ACAGGGTTTCACTAC | 26259 |
rs776822971 | snp | A/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909408 | TGAGGTGGGTGGATC[A/G]CTTGAGGTCAGGAGT | 26259 |
rs776828825 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945487 | AAGCTCATCTTCCAA[A/G]AGTGCCGAGCCAAGG | 26259 |
rs776854703 | in-del | -/T | 1.71968e-05 | 0.00293225 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985429 | AGTCTGGTCATCTTA[-/T]TTTCTATTCTTAGAA | 26259 |
rs776995943 | snp | A/C | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984627 | TGTAGGAAATTTCAC[A/C]TCTAACTTCATGTGA | 26259 |
rs777014785 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938835 | CCCTATTTGGGGCCA[A/G]TCTTGTGATCTAACC | 26259 |
rs777055394 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025531 | CAGCAATTTGACAGG[A/T]GTCTCCAAGAGGCGG | 26259 |
rs777081716 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996880 | TATCACATCTGCCTC[A/G]GGGATTACAGCCTTG | 26259 |
rs777092881 | in-del | -/TG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920113 | TTGAGTTCTGTCTCC[-/TG]TGTTAATTCTTCCGT | 26259 |
rs777119668 | snp | C/T | 1.65696e-05 | 0.00287828 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945374 | TTTAGGTGAGCAAGA[C/T]GTGGAAGGTGATTGC | 26259 |
rs777128618 | snp | A/T | 1.65097e-05 | 0.00287308 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988654 | TAAACAACTCTTACC[A/T]TTTAACAGGTTCAGT | 26259 |
rs777164976 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117006861 | TTTTATCTAAAAATT[A/G]TAAACAATCCATATG | 26259 |
rs777198528 | in-del | -/TG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117013955 | TAAGCGTTTAGAATC[-/TG]TATATTTATGTCTTT | 26259 |
rs777216791 | snp | A/G | 1.65061e-05 | 0.00287277 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945393 | GAAGGTGATTGCAGA[A/G]GATGAGGTGCTGTGG | 26259 |
rs777260778 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992634 | CTTAGCTCCCACTTA[C/T]AAGTGAGAACATGCT | 26259 |
rs777271068 | snp | G/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917524 | CCTGTTGTATTTCTG[G/T]TGCAGTCTCCTCCAC | 26259 |
rs777271516 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922248 | TTCCCCCAGCCAACC[A/T]GTTTTTTTCTTCTCA | 26259 |
rs777307751 | in-del | -/G | 4.9423e-05 | 0.00497082 | frameshift-variant, intron-variant, nc-transcript-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010426 | CCCTCCCAACCTCAT[-/G]GGTCAGTGGCAACAT | 26259 |
rs777331193 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117023223 | TTCAGAGAATCCTGT[C/T]GCTCCACAGCTTTTG | 26259 |
rs777334134 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117031367 | AACTCTTCACCAACC[A/G]TCATCAATAGGTTTT | 26259 |
rs777338037 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947477 | AGGCGGCCCGGCACC[A/G]TGGGTCACTCCTGTA | 26259 |
rs777350156 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117004002 | TTATCTTACTGGAAA[G/T]GTATCGCGATGCTCT | 26259 |
rs777373953 | snp | C/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116980619 | CAAATGAATTTATAT[C/G]AGATTTAAAAAAAAA | 26259 |
rs777397819 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116960898 | GAAAGCTTCAGGCTT[C/T]AAGGAGGGGAGGGGA | 26259 |
rs777401230 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945447 | GCACCTTCCGGATAG[C/T]AGCATCTCTGACTAT | 26259 |
rs777410294 | snp | C/T | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024166 | AGGATCCACGACCTC[C/T]GCAGTGGTAACATCG | 26259 |
rs777413351 | in-del | -/TCTGAAGG | 3.29495e-05 | 0.00405877 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949740 | ACTGAGTGCTCTGCA[-/TCTGAAGG]TCTTTCATTTTTCTC | 26259 |
rs777430223 | snp | A/T | 1.65446e-05 | 0.00287612 | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988625 | TTGATCAAGTCAGGA[A/T]GAATTTATGGGACTA | 26259 |
rs777452928 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117005128 | GAGATCTCTGTGGAA[C/T]CATCTTCTGTTTTGG | 26259 |
rs777459906 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959799 | AACAAAAAATCAGCT[A/G]TGGTCTCTGACCTAT | 26259 |
rs777476431 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016982 | CTCAGTTCTGTTCTG[C/T]TGATCTGTATGTCTG | 26259 |
rs777552343 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019656 | ATGTATGGGAGTGTA[-/T]TATAAGGTGCGCATA | 26259 |
rs777585443 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116972455 | AGTATATTTGTGGAA[C/T]GAATATATTTTTGTT | 26259 |
rs777589771 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117002938 | GTAGTTCAATTCCAC[A/G]TTTCTGTGGATCTTA | 26259 |
rs777638485 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984459 | TGTGGGATATTGAAG[C/T]ACAGGTTTTAGAGCT | 26259 |
rs777656066 | snp | A/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909245 | GCCCTGGGTTTGTAG[A/G]CAGCTAGTTTATTTA | 26259 |
rs777724946 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116940024 | GCATTGCTGAGTCGT[C/T]ATCCCGTTCTTTATT | 26259 |
rs777747171 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985152 | TGTTTTTAAAATAAT[C/T]GAACATATTAAGTAA | 26259 |
rs777787006 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920295 | TTACATGCGGTCTTT[A/G]TTGGAACGGTCTGCT | 26259 |
rs777793164 | snp | C/T | 2.0031e-05 | 0.00316467 | intron-variant | FBXW8 | GRCh38.p7 | 12:116927982 | TGAGTTATTTTCATA[C/T]CTAAAAATTATAAAC | 26259 |
rs777906380 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116942666 | GGCGTGAGCCACTGC[A/G]CCTGGCCAAATTTGC | 26259 |
rs777929415 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116997615 | CATCAGGCAAAGCCT[A/G]GGAGAGAGCAGTCCA | 26259 |
rs777933502 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020768 | TCCCCTCCCCTGAAG[A/T]CGCAGCTCACCCTCT | 26259 |
rs777934281 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008104 | TAAGAAATAATTTAT[C/G]CACTTGTCAAAAAAG | 26259 |
rs777962412 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962191 | TGAGTGGACCAACCT[C/T]CTCTGTGGGAGAAAG | 26259 |
rs777981014 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027007 | GCCCCCAGTGCTCCA[C/T]AGATGATGGAGAGCC | 26259 |
rs777987734 | snp | C/T | 0.000489836 | 0.0156422 | utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116911014 | TGGAACCGAGGAGAA[C/T]GTGGAGCGCCGGGAG | 26259 |
rs778008897 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116925534 | AGTGTATTGGTTTCT[C/T]TTTTTTCCCTGCCAT | 26259 |
rs778031003 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019841 | TTTCTTCTCCAAGGT[A/G]ATTGTTGTTAATGTT | 26259 |
rs778038362 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975700 | ATGTACCTCCTGATA[C/T]ATAATGCACTGGGAA | 26259 |
rs778050766 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944155 | TAAAACAACTTAGAC[A/G]TCACTGTTCTTACTG | 26259 |
rs778055780 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000458 | CACATGCCAGCATGC[A/G]TCAGAATCTACAGGA | 26259 |
rs778063449 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988830 | CAACCAAGTTGCTTT[C/T]GGTGTACAGGGTCTG | 26259 |
rs778105876 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956623 | AGTTTGCCTGTTGGC[C/T]CTTCAGTGGAATTTT | 26259 |
rs778124451 | in-del | -/AT | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909735 | TAGAAGGGAAGGGAT[-/AT]ATATATATACATAAA | 26259 |
rs778152410 | snp | A/G/T | 3.29724e-05 | 0.00406021 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949579 | CTTTCGGGCTGTCCC[A/G/T]AGAGCAGTCTAAACT | 26259 |
rs778192142 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029124 | ATCCAGTAGATGCGT[A/G]TGGAATTTCAAATAC | 26259 |
rs778237164 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913207 | ATTATACTCTACTGT[A/G]TAGCCTCCTTTGGTT | 26259 |
rs778279893 | snp | A/G | 1.65072e-05 | 0.00287286 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028165 | CCTTTCCCTATAACC[A/G]TGTTTAGGGATGTGC | 26259 |
rs778290485 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912028 | ATCCCCTTCAGAAAG[C/T]TGGGAAAATCAAGAA | 26259 |
rs778317191 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016558 | AAAATATTTTCTCCC[A/G]TTCTGTGGGTTGTCT | 26259 |
rs778332875 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924551 | TGCACTTTTATATCC[A/C]TTAACCAACCTCTGT | 26259 |
rs778354237 | snp | A/G | 1.74955e-05 | 0.00295761 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945580 | AGCCTGCAAGGACAT[A/G]GGAATCCAAGCTTTC | 26259 |
rs778411508 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936716 | GCGAATAAATCTGTA[C/T]TGTTTTAAGCAGCTA | 26259 |
rs778413017 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968125 | TGGTATGTGTGAACA[A/G]TGTTAATTTTTTAAT | 26259 |
rs778416672 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117012644 | TTAGAGATGCTGGCC[C/T]AGGCTTGTATAGCTT | 26259 |
rs778429554 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116981779 | CCACAATGACTGGCT[A/G]ATTTTTGTATTTTTA | 26259 |
rs778447908 | snp | A/G | 1.65119e-05 | 0.00287327 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010275 | AAGTATTTGATGTCG[A/G]CCTGGTGTGTGGAAT | 26259 |
rs778493793 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994198 | TGTAAAAGTAGATAC[C/T]AGTACTGGTATAAAA | 26259 |
rs778541582 | in-del | -/G | 1.6477e-05 | 0.00287024 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024236 | TGCAGATGGATGACT[-/G]GAAGATCGTCAGTGG | 26259 |
rs778548510 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988798 | GGCCCGCCTGTCACA[C/T]GTCTAGACGTCTCGG | 26259 |
rs778584640 | snp | C/T | 8.23893e-05 | 0.00641778 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024199 | CTGTCGCTCTCCGCC[C/T]ATCAGCTCAGGGTCT | 26259 |
rs778604361 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995224 | GCGTACGCGGACATG[A/C]TCCCCTTCTGGGCTT | 26259 |
rs778714156 | snp | C/G | | | | | GRCh38.p7 | 12:117004100 | TCAGATTTCCCATCT[C/G]TCTGTCTGTTGCATT | 26259 |
rs778718582 | snp | C/T | | | | | GRCh38.p7 | 12:116972650 | AAGTATGTTGAGGCT[C/T]ATGGGAGCCAGTTCT | 26259 |
rs778759323 | snp | A/G | | | | | GRCh38.p7 | 12:116940301 | AGGCCCACAGACCAT[A/G]TTTTGCAGATGACTT | 26259 |
rs778776921 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117000608 | CCTGGGACCACACTT[C/T]GAGCACCCTGGGGTA | 26259 |
rs778780057 | in-del | -/TGT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922811 | GAGTGTGTGTGTGTG[-/TGT]TTTTTTTCCCTTGAC | 26259 |
rs778809735 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919141 | AAAGCAAAACCGCGG[A/G]TAAGGGGGGACGACT | 26259 |
rs778834055 | snp | A/G | | | downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117032677 | CAGGCAATAATTTAT[A/G]TTTCAGAGATACTCC | 26259 |
rs778839147 | snp | A/G | 3.29663e-05 | 0.00405981 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028119 | TCATCCTGTGACGCC[A/G]TGGCCACTCACTACT | 26259 |
rs778856533 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917808 | CCATCCTGGCTAAGA[C/T]GGTGAAACCCTGTCT | 26259 |
rs778879336 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116957485 | GAAGCCCTCAAGGAT[C/T]GTGTTTCCAACACTC | 26259 |
rs778896712 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116973828 | AGTGAGTATATAGAA[A/G]TTCTTGCAGCTTTTC | 26259 |
rs778916559 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922744 | GTCCAGTAGACTTTG[A/G]GAAAATCTAGTATTC | 26259 |
rs778930940 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010371 | CTCTTGAAGCTGGGT[A/G]ACGTTCTCCGTGACT | 26259 |
rs778945429 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022823 | AGCATTAAAATTGCA[A/G]CATCTTTTCATCCTC | 26259 |
rs778969558 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921363 | TAAATGTTAAGAGAC[A/G]AATTGTTTTTTTGTG | 26259 |
rs778995360 | snp | A/C | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986868 | GCCAACACGGAGATA[A/C]AGTTAAAGGGCTAGA | 26259 |
rs779019930 | snp | A/G | 3.29533e-05 | 0.00405901 | missense, utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024229 | TCTGCTGTGCAGATG[A/G]ATGACTGGAAGATCG | 26259 |
rs779032049 | snp | A/T | 0.000115507 | 0.00759869 | intron-variant | FBXW8 | GRCh38.p7 | 12:117010291 | CCTGGTGTGTGGAAT[A/T]GTGGGCCCACACATT | 26259 |
rs779047650 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116931733 | TACCCATAACTGAAT[A/T]TGTTTATTAGTTTCT | 26259 |
rs779075143 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009894 | ATTCTTTCTTTTCCC[A/G]CCTGTGACGTAAATT | 26259 |
rs779081510 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116996620 | ATTGAAAGTTCACAA[A/G]GTAAATGTCTAATTT | 26259 |
rs779087471 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116944034 | AAACTTGTCTGGCCT[C/G]TCTAATGGCTGCTAG | 26259 |
rs779092050 | snp | G/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978485 | TTTCTGATAGGCAAG[G/T]GTTTATTTACATGGT | 26259 |
rs779112770 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977198 | TCTTTATGTAGACTT[C/T]TCCCCCTGCTTTTTA | 26259 |
rs779139919 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019963 | AGTAGCCTAGAGGGC[A/G]AAGCGCACCCCTCTT | 26259 |
rs779158492 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117029285 | ACCCTCAGGCAGGGC[C/T]CTGCTTTTCTAGGAA | 26259 |
rs779182232 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932633 | CTCTGCCTCCCAGGT[C/T]CAAGCTATTCTCCTG | 26259 |
rs779183858 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963701 | TTTCAGTGACTCAGT[A/G]AATCTCAGAGGTTAT | 26259 |
rs779200230 | snp | A/G | 1.66078e-05 | 0.00288161 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928068 | ATCCAACTGCCTTAC[A/G]AATTGGCAATCAATA | 26259 |
rs779213484 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116914412 | ACGTAGAGAAACCCC[A/G]TCTCTACAAAAATTG | 26259 |
rs779237830 | snp | A/T | 1.66004e-05 | 0.00288096 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024339 | AGGTGCATTCTAGAC[A/T]CTCTTGGGAGTTCCT | 26259 |
rs779239272 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946168 | CACCTGGGAGGCTGG[A/C]GATTCAATGGTAGAG | 26259 |
rs779241342 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117020828 | GAAGTCACTTCCTAC[A/G]TGAGCTCAGCAGTGC | 26259 |
rs779260742 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117001542 | CTTTTCATTTTCAAA[A/G]TAGTATGCAAGTTGC | 26259 |
rs779263436 | in-del | -/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962418 | TGTGTTCAGGGAGCT[-/G]GGGGGCTGGAGCTGA | 26259 |
rs779274720 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116945071 | ATGTAAAAGTTTATA[-/T]TTTTTTGCATTTTAT | 26259 |
rs779403900 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970532 | GCTTTTTAGCGGTGA[A/G]CAGTAGGACCATGTT | 26259 |
rs779463813 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956988 | AATAAACAAAGTCAT[C/G]TAAGGTAACTTGAAA | 26259 |
rs779497337 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116956882 | CTGAGGCAGAAGAAT[C/T]GCTAGAACCCAGGAG | 26259 |
rs779521018 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117024014 | GATGTCCTTATTATC[A/G]ATGTTTGTTTGCAGC | 26259 |
rs779557490 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969355 | TTTCTGTGATAAACA[A/G]CAACTTCTATTCTTT | 26259 |
rs779574847 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116969263 | ATTAAGGGCTCTTCC[C/T]TTTTTAGAGCCCTTG | 26259 |
rs779576974 | snp | C/T | 1.64768e-05 | 0.00287021 | intron-variant | FBXW8 | GRCh38.p7 | 12:116949750 | CTGCATCTGAAGGTC[C/T]TTCATTTTTCTCATA | 26259 |
rs779618725 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116950828 | TAAAATGTGGGCCTG[C/T]GATCAACTGATATGC | 26259 |
rs779624999 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025185 | TTGCTGCCCTCAGCA[C/T]CACTGTGAAGAGACA | 26259 |
rs779638551 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116911414 | CCCGCCCCCAGGACA[A/G]ACCCCTGCAGTGATT | 26259 |
rs779655368 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117015016 | TGACTGGGGACTGTC[C/T]TTGGGGCACAGCCAC | 26259 |
rs779664907 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983906 | TGTCTTCAACTTTAC[A/G]GAAAGGCTAACAGGC | 26259 |
rs779678271 | snp | A/C | 1.65149e-05 | 0.00287353 | missense, downstream-variant-500B, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117024317 | TGTGGGAGGTGTATT[A/C]CGGGTAAGGTGCATT | 26259 |
rs779683110 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983091 | AGTGAGAGGAGACAC[A/G]CGAGTCTCTGAAGAC | 26259 |
rs779741994 | in-del | -/GT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116972567 | TGGGGGCCAGGGACA[-/GT]GTGAGAGGGAAGCTG | 26259 |
rs779745146 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014223 | CTGCTGTTGAGCCTA[G/T]CCAGTGAATCTTTTA | 26259 |
rs779775231 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995348 | TGGGCTCCTGTCCCA[A/G]ACCCTGGATTCTTTA | 26259 |
rs779815951 | snp | A/C | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028069 | AGTTTGCGGTGGACC[A/C]GCTGGCCTTCCAGAG | 26259 |
rs779839246 | snp | A/G | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909532 | TACTCAGGAGGCTGA[A/G]GCAGGAGAATGGCGT | 26259 |
rs779842063 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116919194 | ATATTCATTGATCAG[C/G]TCAGTGCTGGGGAAT | 26259 |
rs779852848 | in-del | -/C | | | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010723 | GAAGGTCCAGGGAGA[-/C]CACTTGGAATATCTT | 26259 |
rs779900819 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116920207 | TCATTTTTTCATGTT[A/G]TTCGTGAATTAGCAG | 26259 |
rs779903761 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116921778 | GTCTTTAGTAATATA[A/T]TTGCTTAGAGGCTAC | 26259 |
rs779911703 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117005538 | ACCTGCTGGAGTCAC[C/G]GCCTCCTCCCCTCCA | 26259 |
rs779932601 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116994291 | AGTAGATACGCAGAC[C/G]AATGGAATAGTACTG | 26259 |
rs779953623 | snp | A/G | 6.63922e-05 | 0.00576123 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928076 | GCCTTACGAATTGGC[A/G]ATCAATATATTTCAG | 26259 |
rs779974665 | in-del | -/AGGTGTATTCCGGGTA | 1.64959e-05 | 0.00287188 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117024308 | ACCAGAAGCTGTGGG[-/AGGTGTATTCCGGGTA]AGGTGCATTCTAGAC | 26259 |
rs780009184 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007209 | ATCATTGACAAAATT[C/G]CAAGTTAAGATTCTA | 26259 |
rs780023685 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116931211 | GCACAGGCTTATTTC[C/T]GGGCTCTCAGTTCTG | 26259 |
rs780036894 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007962 | AAGGTACTCTTCAGA[G/T]AGTTCGGATTCGTTT | 26259 |
rs780037015 | snp | C/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979631 | GTTGCAATCCCAGCA[C/G]TACTCAGAATTAATC | 26259 |
rs780037688 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116963219 | AGAATGGCCTTTGGA[C/G]TGTGCAATATATGTA | 26259 |
rs780055001 | snp | C/G | 8.23757e-05 | 0.00641725 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964739 | GGACACCCGCACCTG[C/G]GACTACGTAGCCCCC | 26259 |
rs780098434 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117019689 | GTTTCAAGAGTAACC[A/G]AGAATGCCCGCGCAT | 26259 |
rs780152363 | snp | C/T | 1.67077e-05 | 0.00289026 | intron-variant | FBXW8 | GRCh38.p7 | 12:116928017 | TTCTTTTTTTTTTCC[C/T]CTCAGAATGAAATGA | 26259 |
rs780179599 | snp | A/C | 4.94564e-05 | 0.0049725 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028128 | GACGCCATGGCCACT[A/C]ACTACTACGACCTCG | 26259 |
rs780188079 | snp | C/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909348 | AAGAGCATCTTTGAG[C/T]CTGGAGTGGTGGCTC | 26259 |
rs780198477 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116962390 | TTTGCTGTCATTTTG[G/T]CTCCGAACTCTTTGT | 26259 |
rs780236886 | snp | G/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978756 | AACTGTTAACCTGTT[G/T]TAAATTTTGTGGTGC | 26259 |
rs780246294 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116965215 | CTCTGCTCAGCCCAA[A/G]GGGAATAGTGAAAAG | 26259 |
rs780247938 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966220 | TTTATTGAGACCCTG[C/G]ATAGATACCATAAGA | 26259 |
rs780308905 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922860 | GATAGATTTTTATAT[C/T]TGCCTATGATGTATG | 26259 |
rs780327881 | in-del | -/TG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116938508 | GTACAAATTTCAGAT[-/TG]TGTTATTTAAAATGA | 26259 |
rs780333262 | snp | C/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116979887 | TTACCTTGGCCTACT[C/G]TGCAGGAGAGAAGTC | 26259 |
rs780355082 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959532 | GAAGGGCCTTAAAAA[A/T]TTTTGTTTTTAGCAA | 26259 |
rs780366773 | in-del | -/T | 3.29603e-05 | 0.00405944 | frameshift-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116945455 | GGATAGCAGCATCTC[-/T]TGACTATTCTTGCTG | 26259 |
rs780384646 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117010168 | ATGTCCCTATACTAT[A/C]AGTAACCTGAAAAAG | 26259 |
rs780387706 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116997862 | ATTCTATCACCCAGG[C/T]CAGAGTGCAGTGGCG | 26259 |
rs780398466 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990691 | TAATGGATACATTTG[A/T]GAAACTACTTAAAGG | 26259 |
rs780402646 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021950 | TGTGGCATCTTGCTG[C/T]GGAGTCTGTTCCTGA | 26259 |
rs780459516 | snp | C/G | 1.66316e-05 | 0.00288367 | splice-acceptor-variant | FBXW8 | GRCh38.p7 | 12:117027393 | TCCCACTGCCTTCCA[C/G]GCACCCGGTGCAGCA | 26259 |
rs780466464 | snp | A/T | 1.64754e-05 | 0.00287009 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988733 | CTGCTGGAGATCTGA[A/T]GTACCTGCTCAAAGC | 26259 |
rs780491844 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116989130 | AAATTTAATGCATAT[A/G]TAGGTACATTTGTAT | 26259 |
rs780533305 | snp | C/G | 3.29609e-05 | 0.00405948 | missense, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985349 | GTCGTGATGTTATCC[C/G]CCAATGAGGAGGGGT | 26259 |
rs780568017 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116916043 | ATGTGTCTTTGAGTT[C/T]TCGTGTATGGCATTA | 26259 |
rs780576868 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117030458 | TTTTCATCAAGCCCC[A/G]CCCTTTCTCTCTCAT | 26259 |
rs780581517 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932967 | AGATATTTTTTGATG[C/T]GGAGTGTGTGTCTTT | 26259 |
rs780585601 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947221 | TATTTCTAATGAACA[C/G]GAAGTCATGTGTTAG | 26259 |
rs780588185 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016996 | GTTGATCTGTATGTC[C/T]GTGTTCTGGCACTAC | 26259 |
rs780648689 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995216 | GATCGGCAGCGTACG[C/T]GGACATGCTCCCCTT | 26259 |
rs780690379 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116991909 | TATGATGCCCACATT[-/A]AGCATGTTACAGGCA | 26259 |
rs780694240 | in-del | -/AA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116914572 | GCGAAACCCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 26259 |
rs780709171 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917398 | TCCCTAGAATCTTTA[A/G]CAGAAGCTGATCCAC | 26259 |
rs780721456 | snp | C/G/T | 3.41042e-05 | 0.00412931 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027361 | CAGGCCCAGTGGACG[C/G/T]CCCCTTACGAGCTCT | 26259 |
rs780783027 | snp | G/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959704 | TACTAGTTAATGAAA[G/T]CTCTTTGGTGGTAAA | 26259 |
rs780806423 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932984 | GAGTGTGTGTCTTTA[A/G]GAAATGATGGAAATT | 26259 |
rs780823964 | snp | A/G | 0.000260193 | 0.011403 | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985435 | GTCATCTTATTTTCT[A/G]TTCTTAGAATCTCTG | 26259 |
rs780830722 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116985106 | CTCATTTCCAAGGTA[C/T]CTCCGTTAAAAAATT | 26259 |
rs780832348 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970706 | TGAATGCAGTAAACA[A/G]CTACCCCCCTGCCCC | 26259 |
rs780885674 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117006499 | CACACCTGGATGCTG[C/T]GGGGCCCGCCTGCCC | 26259 |
rs780902755 | snp | A/G | 1.6596e-05 | 0.00288058 | missense, utr-variant-5-prime, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116928083 | GAATTGGCAATCAAT[A/G]TATTTCAGTATCTGG | 26259 |
rs780934148 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926663 | CCTGTTTTTTTCTGT[A/G]TGGTCAAAATTTCTC | 26259 |
rs780938860 | snp | A/G | 0.000181203 | 0.00951675 | missense, intron-variant, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117010381 | TGGGTAACGTTCTCC[A/G]TGACTTCACGTGTGT | 26259 |
rs780975135 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117014355 | GCATTTTACCTTTAC[C/T]TCGTGGAATATAGCT | 26259 |
rs781030897 | snp | A/G | 1.64885e-05 | 0.00287123 | intron-variant, downstream-variant-500B | FBXW8 | GRCh38.p7 | 12:117010473 | AGTTGGAAGGGCATT[A/G]CCTTGCAGCCCCATG | 26259 |
rs781042285 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116941195 | TGGAAGCATTGCAGG[A/T]TTGCCTGGGCCCCAT | 26259 |
rs781052032 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954982 | GCCTTTTCTTGGCTC[A/G]TCCTCTCCAGCCTCT | 26259 |
rs781056534 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116995536 | CTATTGCTGGCAGAA[A/G]GTATTGGGCAGGAAA | 26259 |
rs781062984 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116937924 | ACACTTTTATTAGCA[A/G]GTCCTTGCAGCTGAG | 26259 |
rs781063287 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117025343 | CATCTCTACAAAACC[A/G]AGATGATTCTGGGCC | 26259 |
rs781089337 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988216 | TTGTAAGTAACTTCT[A/G]GAAGTGGATATCCTG | 26259 |
rs781090373 | snp | C/T | | | intron-variant, synonymous-codon, missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116918714 | AATCCATTGCCCATT[C/T]CTGAAGATGAAGGTG | 26259 |
rs781115932 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116911935 | CTTTCATTAGGATAG[A/G]GTTTCTTATCTTTTT | 26259 |
rs781156211 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116951638 | TACACCTATTAAGTA[C/T]ATTTCACATCATTGA | 26259 |
rs781173634 | snp | C/G | 2.05139e-05 | 0.00320258 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116910995 | ACTGTCTCGTGGCAC[C/G]CGGTGGAACCGAGGA | 26259 |
rs781191867 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116913112 | ATATAGGTTCTGGGC[C/T]CTCCCCAGACCTGCT | 26259 |
rs781205227 | snp | C/T | 1.73905e-05 | 0.00294872 | intron-variant | FBXW8 | GRCh38.p7 | 12:116964877 | ACCACAACCCTCCTC[C/T]CTATTAAGGAAAAAA | 26259 |
rs781217066 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117028137 | GCCACTCACTACTAC[A/G]ACCTCGCACTGGCCT | 26259 |
rs781249504 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117008750 | CAAGAAGAAACGCAC[A/G]TCACTCTCATGTGTG | 26259 |
rs781295186 | snp | G/T | 5.01685e-05 | 0.00500817 | intron-variant | FBXW8 | GRCh38.p7 | 12:116945357 | TGTGTCACTTCTGCT[G/T]TTTTAGGTGAGCAAG | 26259 |
rs781322467 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955457 | CTCTCAAAGTTCAGC[A/G]CCTGTCTGCATTTGT | 26259 |
rs781374357 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116966503 | GCTGCGGTGGTCGTG[C/T]TGTTTGTGGAATCCT | 26259 |
rs781402288 | snp | A/G | 9.88582e-05 | 0.00702989 | missense, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:116964746 | CGCACCTGGGACTAC[A/G]TAGCCCCCTTCCTGG | 26259 |
rs781447395 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116954294 | ATGTTTTTTCATAGT[A/G]TGACTGTAGCCTTTG | 26259 |
rs781452882 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116987219 | ATGTTGACGCTCCCT[C/T]CAGCTCTTCTGGACC | 26259 |
rs781493628 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116967847 | TCTCGACTCACTACA[A/T]CCTCCGTCTCCTGGG | 26259 |
rs781539277 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116970290 | GAGAGACGCGATCTG[C/G]TGCATATTAGCATGA | 26259 |
rs781542691 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998994 | TTATTAATTTCCTCC[A/G]CACTTCAGTCTTCTA | 26259 |
rs781544053 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116948307 | TGTAACCTTGGTTGC[A/G]GCCTTCACACAGCTG | 26259 |
rs781570701 | snp | A/G | 6.59011e-05 | 0.00573988 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988750 | TACCTGCTCAAAGCC[A/G]AAGACTCCGCCAGAA | 26259 |
rs781585590 | snp | C/T | 0.000148276 | 0.00860907 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116988811 | CATGTCTAGACGTCT[C/T]GGCCAACCAAGTTGC | 26259 |
rs781671517 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117009367 | ACTGCACTCCAGCCT[A/G]GGTGACAGAGCAAGA | 26259 |
rs781697734 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116922969 | TGTAATCCCAGCACT[C/T]TGAGAGGCCAAGGCA | 26259 |
rs781722930 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978926 | CTCTTATGACTCCAC[C/T]GGGACAGTTTTAGTT | 26259 |
rs781734732 | snp | A/C/T | 3.30908e-05 | 0.00406749 | synonymous-codon, nc-transcript-variant | FBXW8 | GRCh38.p7 | 12:117027475 | GGTAATGCGAAACGC[A/C/T]GACCTGGACAGCTTC | 26259 |
rs781745348 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116947324 | ACTTCTATTTGGAGC[A/G]TGTAAGGTCCATTTC | 26259 |
rs781757882 | in-del | -/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959250 | TTAGGGTCAGGGGCT[-/G]TGTCCTGCAAACCTG | 26259 |
rs781769946 | snp | C/T | 0.000510899 | 0.0159746 | intron-variant | FBXW8 | GRCh38.p7 | 12:117027552 | TCTTAGTTTGACTGA[C/T]GTATAGAACCCCACC | 26259 |
rs796072236 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116990618 | ATTTTTCATACTTTT[-/T]ATAAATGTTTTCTCC | 26259 |
rs796081312 | in-del | C/TT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912182 | CCTGTTTTTTTTTTT[C/TT]TTCTTTCTTTCTTTC | 26259 |
rs796107443 | snp | G/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116975847 | AGTAATTGCCCCAGA[G/T]TGGAGTCGATGAAGG | 26259 |
rs796109338 | snp | C/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116936900 | TGCTTTGAGCAGAGG[C/G]GTGACAAGGGCTGCC | 26259 |
rs796111789 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116918965 | CCTGTATATGCCATG[-/T]TTTTTTTTTCCTATA | 26259 |
rs796133833 | in-del | -/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955049 | AATGGGGGGGGGGGG[-/C]CCTGTATTAAGCATC | 26259 |
rs796145261 | snp | C/T | | | intron-variant, nc-transcript-variant, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116978214 | TTTTTCGTGACCCTC[C/T]GTGGTTTAGCTGTTC | 26259 |
rs796157183 | in-del | -/TT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116928013 | TTCTTTCTTTTTTTT[-/TT]CCCCTCAGAATGAAA | 26259 |
rs796203057 | snp | A/G | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116984066 | TTGGAATTGGAGCAA[A/G]GCATTAACCAGCCTA | 26259 |
rs796247810 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007262 | TTTAAGATCTCTAAG[-/A]AAAAAAAAAACAGAT | 26259 |
rs796269754 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116943944 | AGACAAGCCTTGAGA[A/G]TAGAGCTTTCTGGCA | 26259 |
rs796276298 | in-del | -/TTTA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924408 | CCATCACCTAAAACG[-/TTTA]TTATTTGTGTTGTAA | 26259 |
rs796296785 | in-del | -/GATCTGTATGTCTGTG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016984 | CAGTTCTGTTCTGTT[-/GATCTGTATGTCTGTG]TTCTGGCACTACCAC | 26259 |
rs796309954 | in-del | AA/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117022356 | CTAAAGAAACTATTA[AA/T]AAAAAAAAAAAACAG | 26259 |
rs796347164 | snp | C/T | | | intron-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116983347 | GCCAGGGGAATGTGC[C/T]GTGGAACCTTTTGTG | 26259 |
rs796350341 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116953800 | CAAAAAAACAAAACA[A/G]AACAAACAAACAAAA | 26259 |
rs796383564 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117021888 | CATCCCGTTGCTTTC[A/G]GCTTCCATGGACGTG | 26259 |
rs796423509 | in-del | -/TTA | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116924287 | ACACTGATAGCATCT[-/TTA]TTTATTTATTTTTAA | 26259 |
rs796481026 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116932645 | GGTTCAAGCTATTCT[C/T]CTGCCTCAGCCTCCC | 26259 |
rs796527671 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116959439 | CTGTGCCACTAAAAT[A/G]TTTCTTGTGACCCTG | 26259 |
rs796625790 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117018024 | TCTGCAAGTGTTATA[A/T]TAAGTTATTCAGAGC | 26259 |
rs796637057 | in-del | -/GG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955037 | TTCCCCTCTTGAAAT[-/GG]GGGGGGGGGGCCCTG | 26259 |
rs796637678 | in-del | -/GTGTGTGTGTGTGTGT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116992762 | GAGTATTATTCCATG[-/GTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 26259 |
rs796638038 | in-del | -/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117016643 | GTTCTATTTGTCTGG[-/T]TTTTTTTTTTTTTTC | 26259 |
rs796652582 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117027607 | CTATGGGCTATACCC[C/T]CAGGCAGGGCCCTGC | 26259 |
rs796724021 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116998555 | AGAGAATGAACTTAG[C/T]GCTAACTCCATTTAT | 26259 |
rs796750419 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116968260 | GCCACCCACTTTTGT[C/T]TGCTCCATTCTGAAG | 26259 |
rs796755147 | snp | A/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912736 | CCTAAGTGCTGGGAT[A/T]ACAGGCGTGAGCCAC | 26259 |
rs796767993 | snp | G/T | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977265 | ATTGATAGTATAATT[G/T]TAAGATTTTTTTTTC | 26259 |
rs796775641 | snp | C/T | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116935261 | TTCTAGAACCAAAGA[C/T]CAGCATATTAGATTA | 26259 |
rs796818199 | snp | A/C | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116926209 | GGAACCAATTGAAGA[A/C]AGCAATGCCTGCAAG | 26259 |
rs796847517 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | FBXW8, LOC100506551 | GRCh38.p7 | 12:116977403 | AAAACACAAATTAAC[A/G]TATTTTTACTTTTGT | 26259 |
rs796856947 | in-del | -/GG | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116955047 | GAAATGGGGGGGGGG[-/GG]CCCTGTATTAAGCAT | 26259 |
rs796893519 | in-del | -/TAATC | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117011977 | ATTCGCTCTTATAAG[-/TAATC]TAATCTAGAGATGGT | 26259 |
rs796904402 | in-del | -/TTTTT | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116912172 | CTTTTTTTTTTCCTG[-/TTTTT]TTTTTTTTTTCTTTC | 26259 |
rs796936444 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW8, LOC100506551 | GRCh38.p7 | 12:116986544 | GAGGCAGGAGAATGG[C/T]GTGAACCCAGGAGGC | 26259 |
rs796948619 | in-del | -/T | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116976637 | TTTTTTTTTTTTTTT[-/T]GTATTTTTATTAGAG | 26259 |
rs796992248 | snp | A/C | | | intron-variant, upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116917702 | AAGCTGACATGAAAA[A/C]GCAGGACTCACTGGG | 26259 |
rs796994204 | snp | C/T | | | upstream-variant-2KB | FBXW8 | GRCh38.p7 | 12:116909119 | TGAGACAGAGTCTCG[C/T]ACTGTCGCCCAAGCT | 26259 |
rs797001673 | snp | A/G | | | intron-variant | FBXW8 | GRCh38.p7 | 12:116946504 | CTCTGGCCTCTCCCC[A/G]TTAGACGCCAGTAGC | 26259 |
rs797009945 | in-del | -/A | | | intron-variant | FBXW8 | GRCh38.p7 | 12:117007261 | TTTAAGATCTCTAAG[-/A]AAAAAAAAAAACAGA | 26259 |