SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1090 | snp | C/G | 0.0663309 | 0.169604 | intron-variant | FBXO25 | GRCh38.p7 | 8:452108 | CTGCAGATTGCACTG[C/G]TAAGATCCTAGTTAC | 26260 |
rs8049 | snp | C/G | 0.316968 | 0.240864 | utr-variant-3-prime | FBXO25 | GRCh38.p7 | 8:468993 | AAAGTCAGAGGCCAA[C/G]GAAATCATTTCTACT | 26260 |
rs873162 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | FBXO25 | GRCh38.p7 | 8:468143 | TAATATGAGAAGTGA[C/T]GACAGAAAAATTAAT | 26260 |
rs874074 | snp | A/C | 0.210605 | 0.246877 | intron-variant | FBXO25 | GRCh38.p7 | 8:467533 | GGTTATCTGATGAGA[A/C]CTTGTTTGCTTTTAA | 26260 |
rs880926 | snp | A/G | 0.233235 | 0.249437 | intron-variant | FBXO25 | GRCh38.p7 | 8:439450 | AATCGTAAAGTTTAT[A/G]TATCTAATTTTGGTT | 26260 |
rs1050909 | snp | G/T | 0.463774 | 0.129618 | utr-variant-3-prime, downstream-variant-500B | FBXO25 | GRCh38.p7 | 8:469368 | GGATCGGGGTATGAA[G/T]TGTGCACACGCAGCC | 26260 |
rs1050910 | snp | C/T | 0.198944 | 0.244731 | utr-variant-3-prime | FBXO25 | GRCh38.p7 | 8:469810 | TAGGGTCAAGGAGCC[C/T]AAGCAAATCATTTCT | 26260 |
rs1448090 | snp | C/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:410700 | CAACTACTGAACATC[C/T]TAAAATGCAAAACTC | 26260 |
rs1530662 | snp | C/T | 0.48818 | 0.0759629 | intron-variant | FBXO25 | GRCh38.p7 | 8:452692 | GGAAGCAGCCTTTCT[C/T]GTCTGGCTGGGAAGT | 26260 |
rs1967362 | snp | C/G | 0.195214 | 0.243923 | intron-variant | FBXO25 | GRCh38.p7 | 8:444001 | CCTCCTCAGTGCTGT[C/G]GCCTTGGGGCCAGCT | 26260 |
rs1992879 | snp | C/T | 0 | 0 | intron-variant | FBXO25 | GRCh38.p7 | 8:437213 | ATGCATTTATATGTA[C/T]TAGACAAATGACCGA | 26260 |
rs2003213 | snp | C/G | 0.338976 | 0.23363 | intron-variant | FBXO25 | GRCh38.p7 | 8:439509 | TCTCTGCCTGTGGTG[C/G]ACCAATTAGATAGCA | 26260 |
rs2034353 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | FBXO25 | GRCh38.p7 | 8:437201 | GTATTAGACAAATGA[C/T]CGACAGAAAATTTAC | 26260 |
rs2053789 | snp | A/G | 0.131038 | 0.219882 | intron-variant | FBXO25 | GRCh38.p7 | 8:451659 | ACAGTGGGAATAGCA[A/G]TCATCAAACCAGGCT | 26260 |
rs2053790 | snp | G/T | 0 | 0 | intron-variant | FBXO25 | GRCh38.p7 | 8:409648 | AAAATATTTTAAAAC[G/T]TGATGACACACAAAT | 26260 |
rs2053791 | snp | A/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:409483 | ACCTAAACTCTACAG[A/T]TAATTCATTTTGGCA | 26260 |
rs2053792 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:409458 | TTGGCAACTCAGTGA[A/G]AAATGAATAGTTTGG | 26260 |
rs2053793 | snp | A/C | | | intron-variant | FBXO25 | GRCh38.p7 | 8:409425 | TGAATTTCTCAGCTG[A/C]TAAGTTTGATTTTTT | 26260 |
rs2053794 | snp | A/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:409274 | GTTATGGTATGCTCT[A/T]TGGATCACAATGAAG | 26260 |
rs2121887 | snp | A/T | 0.460027 | 0.135605 | intron-variant | FBXO25 | GRCh38.p7 | 8:420046 | catgtgatgcccaac[A/T]taatttattgttagg | 26260 |
rs2241989 | snp | A/C | 0.293807 | 0.246132 | intron-variant | FBXO25 | GRCh38.p7 | 8:451789 | TGCCAGTAATTCTCT[A/C]TTTATTTAGTTGTTG | 26260 |
rs2241990 | snp | C/G | 0.207253 | 0.246318 | intron-variant | FBXO25 | GRCh38.p7 | 8:452556 | TGAGGCAGATCCGTG[C/G]TAGTGATGTTCAGCA | 26260 |
rs2278765 | snp | C/T | 0.311859 | 0.242226 | intron-variant | FBXO25 | GRCh38.p7 | 8:456963 | GAGGTCAGGTGATTT[C/T]GAGAACCAAACTCAT | 26260 |
rs2278766 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXO25 | GRCh38.p7 | 8:458243 | GACACCTTGCGACGC[A/G]TGACATGGAGAGCTC | 26260 |
rs2278767 | snp | A/C | 0.239614 | 0.249784 | intron-variant | FBXO25 | GRCh38.p7 | 8:458958 | CTCAGCACTCGGTAG[A/C]TGCCGCTCCTGAGTG | 26260 |
rs2290073 | snp | C/G | 0.181022 | 0.240296 | intron-variant | FBXO25 | GRCh38.p7 | 8:450168 | TTCTTTTATCTTTAC[C/G]CAGTACACATACTGT | 26260 |
rs2335278 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:437764 | TTTTTTTACTTTATC[A/G]TATGCATTTATCATA | 26260 |
rs2335279 | snp | C/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:437864 | GAGAGGATTGTCTTG[C/T]AGTTCTACTAAATAA | 26260 |
rs2335280 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:437876 | TTGTAGTTCTACTAA[A/G]TAATTTGATTTTCCA | 26260 |
rs2335281 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:439462 | TATATATCTAATTTT[A/G]GTTATTTGATAAATT | 26260 |
rs2335516 | snp | A/G | 0.487558 | 0.0778863 | intron-variant | FBXO25 | GRCh38.p7 | 8:453890 | CCACTTTGGGAGGCC[A/G]AGTCAGGTGGATCAC | 26260 |
rs2878381 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:437827 | GTTTTAAATGTTTAT[A/G]GCAACACTTACTACA | 26260 |
rs2933479 | snp | C/T | 0 | 0 | intron-variant | FBXO25 | GRCh38.p7 | 8:440495 | AGCCGTGAAGAGCTT[C/T]TTCATTACGACTTTA | 26260 |
rs3195129 | snp | G/T | | | upstream-variant-2KB | FBXO25 | GRCh38.p7 | 8:405879 | tccttccctctctcc[G/T]ttcttttcttccttt | 26260 |
rs3214778 | in-del | -/C | | | intron-variant | FBXO25 | GRCh38.p7 | 8:465200 | GGAACAGGGCCCCCC[-/C]TTCTGTGTAATTCCT | 26260 |
rs3217583 | in-del | -/CATA | 0.343254 | 0.231956 | intron-variant | FBXO25 | GRCh38.p7 | 8:452423 | CGTTCCCCATGCATA[-/CATA]GGTGGGTTGTGCTAA | 26260 |
rs3735919 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | FBXO25 | GRCh38.p7 | 8:469514 | TTCAACACAATTGAA[C/G]TTTAGACTGCACTGG | 26260 |
rs3735920 | snp | C/T | 0.00755907 | 0.0610114 | utr-variant-3-prime, downstream-variant-500B | FBXO25 | GRCh38.p7 | 8:469391 | ACAGAGACCACTGCC[C/T]GTTGTTGGGCTGCGT | 26260 |
rs3735922 | snp | A/T | 0.261056 | 0.249755 | intron-variant | FBXO25 | GRCh38.p7 | 8:463414 | GCCAGGAAAGGTCAC[A/T]GGCTGCAATCCGCCT | 26260 |
rs3735923 | snp | C/T | 0.286042 | 0.247388 | intron-variant | FBXO25 | GRCh38.p7 | 8:463288 | CCCCTACCCCAATAT[C/T]TGGTAAAATATATCT | 26260 |
rs3735924 | snp | A/G | 0.251493 | 0.249996 | intron-variant | FBXO25 | GRCh38.p7 | 8:463193 | TTAGTTTGTTTCACC[A/G]AAATTTAATCCTGAA | 26260 |
rs3735925 | snp | C/T | 0.322245 | 0.239334 | intron-variant | FBXO25 | GRCh38.p7 | 8:453304 | AGATGCCAGGCAGCA[C/T]GCAACCACTAATGAA | 26260 |
rs3779746 | snp | G/T | 0.0291137 | 0.117086 | utr-variant-3-prime, downstream-variant-500B | FBXO25 | GRCh38.p7 | 8:469066 | TGAACTATATATATA[G/T]AGAGAGAGAGTACGC | 26260 |
rs3808392 | snp | A/G | 0.151334 | 0.229706 | upstream-variant-2KB | FBXO25 | GRCh38.p7 | 8:406594 | CCTTCAGGTGTTCTC[A/G]TGGCCTGAGGACGCG | 26260 |
rs3840686 | in-del | -/GCG/GCGTGCTG/GCGTGGGA/GCGTGGGG | 0.17128 | 0.237922 | upstream-variant-2KB | FBXO25 | GRCh38.p7 | 8:406754 | CGTGGGGGCGTGGGG[lengthTooLong]TGGGGCTCGGGTGCG | 26260 |
rs3841577 | in-del | -/AAT | 0.29046 | 0.246704 | intron-variant | FBXO25 | GRCh38.p7 | 8:450200 | AAAAACAATTGTGTA[-/AAT]AATGTGATAACATCA | 26260 |
rs3857917 | snp | C/G/T | 0.431177 | 0.172264 | intron-variant | FBXO25 | GRCh38.p7 | 8:439309 | CGAGGCTTGGGAGGT[C/G/T]CATGCAGGGCAGTGC | 26260 |
rs3857918 | snp | A/G | 0.494526 | 0.0520291 | intron-variant | FBXO25 | GRCh38.p7 | 8:442670 | AGAGGGGGTTTTGCC[A/G]TATGGGTCAGGCTGG | 26260 |
rs3873815 | snp | C/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:435836 | TTCCCTTCTGTTTTT[C/T]GATTAATACGCAGCA | 26260 |
rs3925990 | snp | G/T | 0.388775 | 0.207946 | intron-variant | FBXO25 | GRCh38.p7 | 8:442468 | GTTATTTCCACTTTA[G/T]TTTTTTATTTTGTAT | 26260 |
rs3931132 | snp | A/T | 0.124197 | 0.216212 | intron-variant | FBXO25 | GRCh38.p7 | 8:437088 | GCAAATTATAGTAGT[A/T]TGTGGTACACAGACA | 26260 |
rs3936435 | snp | C/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:437204 | TATGTATTAGACAAA[C/T]GACCGACAGAAAATT | 26260 |
rs3936436 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:437132 | AGGTATTTCTGTTTA[A/G]AAAAGTAAATTTGAA | 26260 |
rs3936437 | snp | C/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:436945 | TGACCAAAGATGAGA[C/G]AGCAGGGCACCCAGC | 26260 |
rs3965385 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:446625 | CAACACTAAAACAAG[A/G]AATTTAATAACAATA | 26260 |
rs3965448 | snp | A/T | 0 | 0 | intron-variant | FBXO25 | GRCh38.p7 | 8:435828 | TGCCTGTTTGCTGCG[A/T]ATTAATCAAAAAACA | 26260 |
rs3965449 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:437912 | TAGTCTAAGTTGTCC[A/G]TAATGTCACTCAGTA | 26260 |
rs3965450 | snp | G/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:437922 | TGTCCATAATGTCAC[G/T]CAGTATTATTAGAAT | 26260 |
rs4045403 | in-del | -/CT | | | intron-variant | FBXO25 | GRCh38.p7 | 8:409750 | CCTAGTTGTTTTTTT[-/CT]GTCTCCATGTTTTTC | 26260 |
rs4045404 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | FBXO25 | GRCh38.p7 | 8:446718 | TGCTTGGCCTAACCT[A/C/G]ATCTTATCTCTGGCC | 26260 |
rs4045405 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:446863 | TTTGTGGCTCAGTAT[A/G]TGACTTAGTGATTTC | 26260 |
rs4045406 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:446955 | TTTTCAGAGAAATAA[A/G]AGGCAGATGCAATTC | 26260 |
rs4045407 | snp | C/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:447020 | GCAGCTAAGCCTGGG[C/T]AGTGATACTATAGGC | 26260 |
rs4045408 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | FBXO25 | GRCh38.p7 | 8:447028 | GCCTGGGCAGTGATA[A/C/G]TATAGGCGGAACTGA | 26260 |
rs4045409 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:447036 | AGTGATACTATAGGC[A/G]GAACTGAGCAGAAGG | 26260 |
rs4045410 | snp | C/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:447055 | CTGAGCAGAAGGGCT[C/T]AGGCTAACAAAAGCA | 26260 |
rs4045414 | snp | C/T | 0 | 0 | intron-variant | FBXO25 | GRCh38.p7 | 8:420221 | AGGCTGTGCACCTTC[C/T]TCataaggtaccagc | 26260 |
rs4045415 | snp | C/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:420238 | Cataaggtaccagca[C/G]aggcctacgtcagta | 26260 |
rs4045416 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:420247 | ccagcagaggcctac[A/G]tcagtagctaagatg | 26260 |
rs4045417 | snp | C/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:420334 | gaatatgctctccaa[C/T]cctgctactgggaat | 26260 |
rs4045418 | snp | C/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:420416 | tacactgccttagga[C/G]ctggcagtctcactc | 26260 |
rs4045419 | snp | C/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:420431 | gctggcagtctcact[C/T]ctaggtgtttaccca | 26260 |
rs4045420 | snp | A/C | 0.0733688 | 0.176922 | intron-variant | FBXO25 | GRCh38.p7 | 8:420458 | cccaaggtaagtgaa[A/C]attcatgctcacaca | 26260 |
rs4045703 | snp | C/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:439285 | TCTGACAGCCAGGCA[C/T]GAACAGCCCGAGGCT | 26260 |
rs4045704 | in-del | -/TTA | | | intron-variant | FBXO25 | GRCh38.p7 | 8:439478 | ATTTGATAAATTANN[-/TTA]NNTCTGAAGTACTTC | 26260 |
rs4045705 | snp | C/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:439822 | cctgcaatcccagca[C/T]tttgggaggctgagg | 26260 |
rs4045706 | in-del | -/TT | | | intron-variant | FBXO25 | GRCh38.p7 | 8:440322 | GTGTTAGCCACTATT[-/TT]GATTTTCTTTTGAGG | 26260 |
rs4045707 | snp | G/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:440324 | GTTAGCCACTATTTT[G/T]ATTTTCTTTTGAGGA | 26260 |
rs4298475 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO25 | GRCh38.p7 | 8:406259 | CTGCGGCTCCTGGAC[C/G]CACCTGGCCTTCTCG | 26260 |
rs4481570 | snp | A/C | 0.112631 | 0.208878 | intron-variant | FBXO25 | GRCh38.p7 | 8:410842 | TTCTGACTATAAGTC[A/C]GTTTAGCAAGGTTTG | 26260 |
rs4493890 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:422889 | TTGGGTATGTGTTAC[A/G]GGAGGTACACAGGTC | 26260 |
rs4495405 | snp | A/G | 0.318656 | 0.240388 | intron-variant | FBXO25 | GRCh38.p7 | 8:428142 | TGTTGATTCTTCTCT[A/G]TTCTCTTCTCTTCCT | 26260 |
rs4735938 | snp | A/G | 0.497502 | 0.035255 | intron-variant | FBXO25 | GRCh38.p7 | 8:408273 | TGTTTTAGTGCCTTT[A/G]TATTTAGGTTCATCA | 26260 |
rs4735985 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | FBXO25 | GRCh38.p7 | 8:440095 | TCCCAGGCGGGGACT[C/T]GAGGGTGAGGCAGGG | 26260 |
rs4996317 | snp | C/G | 0.464416 | 0.128553 | upstream-variant-2KB | FBXO25 | GRCh38.p7 | 8:405642 | CTCAGACACTTTTTG[C/G]TTTACACAACAATCC | 26260 |
rs4997280 | snp | A/G/T | 0.00279242 | 0.0372774 | intron-variant | FBXO25 | GRCh38.p7 | 8:420626 | ACAAACTATTAATTC[A/G/T]CACAACATGGATGAA | 26260 |
rs5000141 | snp | C/G | 1.65124e-05 | 0.00287331 | utr-variant-5-prime, missense | FBXO25 | GRCh38.p7 | 8:413150 | AAGATGGCTGGAAGA[C/G]ATGTGAATCTTGTAG | 26260 |
rs5000148 | snp | A/T | 0.460589 | 0.13473 | intron-variant | FBXO25 | GRCh38.p7 | 8:412816 | TTTCAGGTATGAGCT[A/T]GAATGTCACCTCTGG | 26260 |
rs5008929 | snp | A/G | | | upstream-variant-2KB | FBXO25 | GRCh38.p7 | 8:405088 | AATTGTGAGGATGCT[A/G]GCCAATTGGGCTAAA | 26260 |
rs5009624 | snp | C/G | 0.112983 | 0.209108 | intron-variant | FBXO25 | GRCh38.p7 | 8:409037 | AAATACATTCCCATT[C/G]AAAGCCGTGGGTCAT | 26260 |
rs5009626 | snp | C/T | 0.49703 | 0.0384237 | intron-variant | FBXO25 | GRCh38.p7 | 8:408946 | GTTTTTTTGTGTTTG[C/T]AAATTCCCAAAATAA | 26260 |
rs6651443 | snp | C/T | 0.368934 | 0.219897 | intron-variant | FBXO25 | GRCh38.p7 | 8:451493 | TATTACACTCTGTTT[C/T]TATATTACAGAAGTT | 26260 |
rs6981182 | snp | A/G | | | intron-variant | FBXO25 | GRCh38.p7 | 8:440444 | GAAGGTCACAATGGA[A/G]TCAAGGACAGAGACC | 26260 |
rs6981190 | snp | C/G | 0.151419 | 0.238843 | intron-variant | FBXO25 | GRCh38.p7 | 8:432197 | tctcaacaggtgatc[C/G]gataaccaagacggc | 26260 |
rs6981545 | snp | G/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:440642 | gtgctcaatgtgcag[G/T]tttgttacataggta | 26260 |
rs6995668 | snp | A/G | 0.138207 | 0.223612 | intron-variant | FBXO25 | GRCh38.p7 | 8:418366 | tttttttgagatgga[A/G]tcttgctctgtcacc | 26260 |
rs6996501 | snp | C/T | | | intron-variant | FBXO25 | GRCh38.p7 | 8:440694 | ctgcacccatcaacc[C/T]gtcatctacattagg | 26260 |
rs6997120 | snp | A/G | 0.240765 | 0.249829 | intron-variant | FBXO25 | GRCh38.p7 | 8:445994 | AGTCTTCCATAATGT[A/G]GCATGTCGGACTGTA | 26260 |
rs6997615 | snp | C/T | 0.496175 | 0.0435625 | intron-variant | FBXO25 | GRCh38.p7 | 8:445661 | AGTTTGAGACCAGCC[C/T]GGCCAACATGGTGAA | 26260 |
rs6998464 | snp | C/T | 0.497085 | 0.0380671 | intron-variant | FBXO25 | GRCh38.p7 | 8:432957 | ATTCTATTATAAATA[C/T]GAGAGTATCTTGTAT | 26260 |