SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11279 | snp | G/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610721 | TAGCATGTCTCAACA[G/T]CCAGCCTGAGGTAGG | 6468 |
rs14467 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610801 | GGTTTCAAAGCAAAA[C/T]CAGGCCACAGTGCCC | 6468 |
rs888505 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671463 | AAGAATAGCAAGTTT[A/G]TTTGAGATACTGGGT | 6468 |
rs1035291 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677087 | caccaacaatgtagg[A/C]gagtttcTTATTGGT | 6468 |
rs1468973 | snp | G/T | 0.326506 | 0.238006 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632233 | TGGGTTGAGAGAGGG[G/T]TGCGTGTGTGTGTGT | 6468 |
rs1544720 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659496 | GCTTAGTTTTCCCAC[C/T]GCTGGTCTCTAGGTA | 6468 |
rs1549065 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653151 | TCCCTCTCTCCCTGA[C/T]GTGCAGTCATGTCTG | 6468 |
rs2080698 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654723 | AAGGATGACACAGAT[A/G]TACATTTATGGAACC | 6468 |
rs2080699 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654599 | TGGATTTCTGTTGAT[A/G]TTTACTTACTTTTTA | 6468 |
rs3095789 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627783 | AGTCCATTCATGGAA[A/G]CTTGGCCTTTGCTTC | 6468 |
rs3095790 | snp | A/C | 0.336839 | 0.235922 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626924 | GATTTACATCCCCAC[A/C]CCACCCTCATCCCTG | 6468 |
rs3095791 | snp | A/G | 0.19646 | 0.2442 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624079 | tgtctgtctgtgtct[A/G]tgtgtgtctagtcct | 6468 |
rs3127230 | snp | C/T | 0.381503 | 0.21262 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632746 | CCCCTTAAACAACTG[C/T]TCCATGTGCTCCTAA | 6468 |
rs3127255 | snp | C/T | 0.332106 | 0.236133 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610477 | ACAGGTGACCCTCCA[C/T]ACCCCAAAGGGTAAG | 6468 |
rs3127256 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615217 | GAGCCTTGGCTGTTG[C/G]ACAGCTTGTGTGGGA | 6468 |
rs3127257 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620339 | TCTGGGAAAGACAGC[G/T]CTAGAGAGTCATCCT | 6468 |
rs3127258 | snp | C/T | 0.334412 | 0.235318 | intron-variant | FBXW4 | GRCh38.p7 | 10:101623403 | aaacataaataaata[C/T]agattttaaaaaaga | 6468 |
rs3758559 | snp | A/G | 0.322483 | 0.239262 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685475 | CTTAGTGTCTGATAG[A/G]AATCCCTGTAAAATT | 6468 |
rs3901642 | snp | A/C | 0.322483 | 0.239262 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669141 | GTAACTCACACAATC[A/C]TCCCATCCCCCACCC | 6468 |
rs3902130 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668236 | ACTTCTGATTCCCCA[A/G]TGTAAAGTTGGCTGG | 6468 |
rs3925644 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669997 | gaggctgaggcgggt[A/G]gatcatgaggtcagg | 6468 |
rs3925645 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669946 | aacacagcaaaaccc[C/T]gtgtctactaaaaat | 6468 |
rs3925646 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669815 | gtgagctgatattgc[A/G]ccactgcactccagc | 6468 |
rs4081695 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666924 | GAAACAAAAAAAGAA[C/T]GAAAAAAAAACCACC | 6468 |
rs4081696 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670705 | ACTCATAAGAAAGAA[C/T]AGAGAAATAAAGAAG | 6468 |
rs4244347 | snp | A/C | 0.431473 | 0.171952 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692888 | TGGCAGAGCCTAATA[A/C]AGTGTAAAACAGTAA | 6468 |
rs4326724 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673991 | GACTTCTCATGGGTA[C/T]GCAGAGCTTACAAAA | 6468 |
rs4917943 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664468 | ACATCCCCTCATATT[C/T]TCCATGAGGAGTCCA | 6468 |
rs4917944 | snp | A/G | 0.377977 | 0.21476 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664553 | GGAGGGGAACTGAAG[A/G]TGGTCATTGAGGGCA | 6468 |
rs4919563 | snp | A/G | 0.381308 | 0.21274 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637159 | gaggctgaggcgggc[A/G]gatcacgaggtcagg | 6468 |
rs4919564 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642659 | ACCAAATTCTACCTC[C/T]GAAGCCTCCTTGGTA | 6468 |
rs4919565 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654710 | TATGACATCTTTTGG[G/T]TCCATAAATGTATAT | 6468 |
rs4919566 | snp | A/C | 0.195526 | 0.243993 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655128 | TGCCACCATGCCTGG[A/C]CTATTTATGTGTTCT | 6468 |
rs4919567 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655148 | ttatgtgttcttaat[A/G]taagtctttgtacat | 6468 |
rs4919571 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664113 | GAACTCAAAGTAAAG[G/T]AAGAAAGGAAAGAAG | 6468 |
rs4919572 | snp | A/G | 0.323197 | 0.239044 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664167 | TGCTTTCTCTCAGTC[A/G]TGAGGACCTCAAATT | 6468 |
rs4919573 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666505 | AAAGAAGCTGAAGGG[A/C]CTAAACGAAGTGGGT | 6468 |
rs4919578 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670909 | AGTCCCTAGCTCAGA[A/T]GTCTTGCAAAGAGAT | 6468 |
rs4919584 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688096 | GGGGCAGGAGAAGGC[A/G]GAGGAATGAACTGGC | 6468 |
rs5787442 | in-del | -/AG | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691401 | CCAGAAAACCCGAGC[-/AG]TGACCCTGCTCTTTA | 6468 |
rs6584435 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643518 | GGATGCCGCAGGCAT[A/G]TGCACGCTTTGCATT | 6468 |
rs6584436 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646788 | TTTTACATTTTGGTT[C/T]TGGGGTATTTAGTTG | 6468 |
rs6584437 | snp | A/T | 0.0596104 | 0.162024 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648486 | TTCTGGGGACTGATT[A/T]TACTTTGAACATGAG | 6468 |
rs6584438 | snp | C/T | 0.322959 | 0.239117 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655677 | GCAGCTGCAACAAGG[C/T]GGAAAATAGCAGGAG | 6468 |
rs6584439 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656827 | ATATCCTATAAGGTT[C/G]TCTCTTGTTACTTGA | 6468 |
rs6584441 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666960 | TCTAGGGCTGGGCAC[A/G]GTGGCTCACAACTGT | 6468 |
rs6584442 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688475 | GGATAAAATGAAGAA[A/C]TGACTCAAAATTGAG | 6468 |
rs6584443 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691868 | CCATTATCATGAATA[A/C]AATCATCCTAGAATA | 6468 |
rs6584444 | snp | C/T | 0.400147 | 0.19989 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696052 | ATTTTAATGTAACTA[C/T]TAGAAAATTTAAAAT | 6468 |
rs7068187 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682560 | AAACTAAAAAGGGAG[C/T]ACTCTGGATCATAGC | 6468 |
rs7071326 | snp | A/G | 0.372391 | 0.217992 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674413 | TAATTTGAAGTGTAA[A/G]TGGGAAGTTTCAAGG | 6468 |
rs7072170 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652867 | GCTCCTAGTTTTCCT[C/T]CTGCCTCTGATTGGA | 6468 |
rs7078354 | snp | C/T | 0.37778 | 0.214877 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648812 | GAAAGTCAGGTTTTC[C/T]GATCAGTATTGTTCC | 6468 |
rs7084405 | snp | G/T | 0.0532157 | 0.154195 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682521 | CTTCTCTTGAATTAG[G/T]TCTAAAATTAATGAG | 6468 |
rs7087836 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650726 | TCTGCCACCAGCCTC[C/T]AGGGCCGAAGACCCT | 6468 |
rs7090062 | snp | A/G | 0.12932 | 0.218944 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648257 | ACAGGTTGGGAGGAA[A/G]AAAGCAAAAATTCTG | 6468 |
rs7095907 | snp | C/G | 0.0535932 | 0.154675 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672663 | AGGTCCTCTGTTTTT[C/G]AGTTCACGCCACATT | 6468 |
rs7478084 | snp | A/C | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637420 | aaaaaaaaaaaaGCC[A/C]CCATGagccaggcat | 6468 |
rs7478123 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637605 | cccatctacttggga[A/G]gctgaggcatgagaa | 6468 |
rs7895811 | snp | A/T | 0.398174 | 0.201356 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681398 | cgtctcaaaaaaaaa[A/T]aataataataataat | 6468 |
rs7896681 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668870 | TCTCAGACGTACAGG[A/G]CTATCCCAAGACAGC | 6468 |
rs7898842 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648049 | CAGGTCACCCAATCA[C/T]CAGGGAGGTCCCTGT | 6468 |
rs7904157 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675690 | GATGTTCCCTATCCA[C/T]TGCAACCAATCAACA | 6468 |
rs7911220 | snp | A/G | 0.0107246 | 0.0724382 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695385 | TGCCTGAGGCCACAA[A/G]AGGACCCGCTGCCCT | 6468 |
rs7914471 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648527 | GCAGCAGTGGCAACA[A/G]GAAAAGGAGTCAGAA | 6468 |
rs7916943 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684303 | tactttatttttgta[A/T]ttttagtagagacag | 6468 |
rs9419933 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619590 | cgtgaacccgggagg[C/T]gttaggcaacggctg | 6468 |
rs9651449 | snp | C/T | 0.259674 | 0.249813 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631199 | AAGAGACAGTGCAGA[C/T]AGAAAATTTAAATTC | 6468 |
rs9651450 | snp | C/T | 0.287085 | 0.247234 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632388 | AAAGCAGGGTTTCTG[C/T]GGAGGAGTGCATTCC | 6468 |
rs9651451 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665538 | ATGAGACACATCGAG[A/G]CCTTAGCAGAGGGTC | 6468 |
rs9731161 | snp | A/T | 0.0543475 | 0.155628 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685696 | TGAAACTTGCTTTTT[A/T]AAAAAAAAATGACAT | 6468 |
rs10564210 | in-del | -/ATTT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680062 | TGCACAAAAGTCATT[-/ATTT]CATTCCTTTTTATGG | 6468 |
rs10688145 | in-del | -/AAACA/AACAA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641643 | AAAAAAACAAAACAA[-/AAACA/AACAA]TACACATACACCTTA | 6468 |
rs10786640 | snp | A/T | 0.190205 | 0.242744 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632876 | ACAAGAAGCATGCAA[A/T]AAGACAAGCTATACA | 6468 |
rs10786641 | snp | A/G | 0.287606 | 0.247155 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633122 | CATAAGACAGAAATA[A/G]TAATAGTACCTAGGC | 6468 |
rs10786642 | snp | A/G | 0.287606 | 0.247155 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633169 | AATTATATGGGAAGT[A/G]TAAATTAGTTCAACC | 6468 |
rs10786643 | snp | A/G | 0.191775 | 0.243125 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634284 | AACTTTACTAAAGAA[A/G]ATAGAATTGTTGAAT | 6468 |
rs10786644 | snp | C/T | 0.190205 | 0.242744 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636889 | CCACTGCACCCAGCC[C/T]AGGATTACATTTAAA | 6468 |
rs10786645 | snp | C/G | 0.0599851 | 0.162463 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659694 | TGAGGTTGTAGTAGA[C/G]TTTCTTCTGAATACA | 6468 |
rs10786646 | snp | A/G | 0.377977 | 0.21476 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679345 | TGCCCAATGCCTTAC[A/G]CATATCAGTAAGTGC | 6468 |
rs10883665 | snp | A/G | 0.18325 | 0.240924 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614476 | GAAAATGTCATGGCC[A/G]TAAGTATCTGCAGTC | 6468 |
rs10883666 | snp | G/T | 0.277334 | 0.248501 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615355 | CCCAGGCCTCCAGGA[G/T]CCACTAAGGGCTGGG | 6468 |
rs10883667 | snp | A/T | 0.186737 | 0.241863 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625092 | GCACACCATAAAAAC[A/T]GATCTCTAGACGTGA | 6468 |
rs10883668 | snp | A/G | 0.190205 | 0.242744 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639077 | CAAGCCCTGGTGCAC[A/G]TGTCAACTCCCTGCA | 6468 |
rs10883669 | snp | A/G | 0.209997 | 0.246779 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641859 | ATATCACTGTATAGT[A/G]TATCAATAGACACAC | 6468 |
rs10883670 | snp | C/T | 0.254944 | 0.249951 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642127 | GCCGAGACTGTGCCA[C/T]TGCACTCCAGCTTGG | 6468 |
rs10883671 | snp | G/T | 0.174932 | 0.238463 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654105 | CAGACCGGCGACAGA[G/T]CGAGACTCCGTCTTA | 6468 |
rs10883673 | snp | C/T | 0.322959 | 0.239117 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664955 | TCATATTTAATATGA[C/T]GAAACTGAGGCTGGG | 6468 |
rs10883674 | snp | A/G | 0.321053 | 0.23969 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665811 | AGCCTAACACATTCC[A/G]GAGGAGGAGGCTGGA | 6468 |
rs10883675 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684009 | CACTGTGTCACCCAG[A/G]CTGGAGTGCAGTAGC | 6468 |
rs10883676 | snp | A/C | 0.175897 | 0.238765 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685568 | CATATATGAACTTTA[A/C]CTCAAAGGATATAAG | 6468 |
rs10883677 | snp | A/T | 0.322959 | 0.239117 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685702 | TTGCTTTTTTAAAAA[A/T]AAATGACATTTACCT | 6468 |
rs11191065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613500 | TGGACACTTCACAGG[G/T]ATGTCCAGGTAAGAG | 6468 |
rs11191067 | snp | G/T | 0.185788 | 0.241613 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620125 | GGCGCTCCTCAAGTT[G/T]CAGCAGTGACAGGTT | 6468 |
rs11191068 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621511 | ccagcctgggtgaca[A/G]agcaagtccctgtct | 6468 |
rs11191069 | snp | G/T | 0.170733 | 0.237101 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628372 | CTGACCATCCTTCTA[G/T]TCCTTTCCATACTCA | 6468 |
rs11191070 | snp | C/T | 0.190205 | 0.242744 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637105 | AAAGCCACCATGggc[C/T]gggcacggtggctca | 6468 |
rs11191071 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638483 | GACACATACTGGATG[C/T]CCTGCAAAAAAAAAA | 6468 |
rs11191072 | snp | G/T | 0.289683 | 0.24683 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640309 | GCTTGAGGGATGGGA[G/T]TCTAGTCTTCAAGGG | 6468 |
rs11191073 | snp | A/G | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640818 | accctgcccaaccTA[A/G]ACTCTTCCTTCCCCC | 6468 |