SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6290418 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Fbxl5 | Mm_Celera | 5:43783908 | TGTGATTTTTCTCAT[A/T]TTAACTATAAATACA | 242960 |
rs6291055 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Fbxl5 | Mm_Celera | 5:43784052 | AGCTACTTTGGAATT[C/T]GGCTATTTCACAGGA | 242960 |
rs45649325 | snp | A/G | | | intron-variant | Fbxl5 | Mm_Celera | 5:43752523 | TTGACATGAAAGAGG[A/G]AATTTTTTTAGACAG | 242960 |
rs45664421 | snp | A/G | 0.35503 | 0.226867 | utr-variant-3-prime | Fbxl5 | GRCm38.p3 | 5:43744764 | CTGCTGCACCAAGAG[A/G]CCAATTTATCCTATA | 242960 |
rs45781315 | snp | A/C/T | 0.391111 | 0.206368 | intron-variant | Fbxl5 | Mm_Celera | 5:43760582 | ATGAAATTATATGAA[A/C/T]GCGAACAGTGTACTC | 242960 |
rs45876710 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl5 | Mm_Celera | 5:43762950 | CCAGTCACCTATACC[A/G]TGAATGGACGAGAGG | 242960 |
rs45918196 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl5 | Mm_Celera | 5:43765850 | AATCAGCAAGCGTAT[A/C]CTCAGCCAGATTATG | 242960 |
rs45991650 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Fbxl5 | GRCm38.p3 | 5:43755641 | TTCTTAAAAGTCACA[C/G]TATCAGAAGTGAGCT | 242960 |
rs46016840 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43748491 | AGGGCTTCTAAACCC[G/T]CACCAAGCATTTCTG | 242960 |
rs46026612 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43762141 | TATTACAGCAATTCT[C/G]ATTATGTACCTGGAA | 242960 |
rs46264443 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fbxl5 | Mm_Celera | 5:43765673 | TGTTAAGAACCCGTG[A/G]GTTAAACTATCACAG | 242960 |
rs46389036 | snp | A/G/T | 0.260355 | 0.249785 | intron-variant | Fbxl5 | Mm_Celera | 5:43763442 | TTCTCTATAGTGATT[A/G/T]GTCAGCAATGTACAG | 242960 |
rs46399597 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fbxl5 | Mm_Celera | 5:43749048 | CTTATATCCATTACG[C/T]AAAACAAAGTACATT | 242960 |
rs46463997 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Fbxl5 | Mm_Celera | 5:43774193 | ACCAACTGAAGAGGT[A/G]TATTTTTAAGAAAAC | 242960 |
rs46485773 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Fbxl5 | Mm_Celera | 5:43750499 | CAAAGAAATCACTGT[A/G]TCTAGAAAATCAAGT | 242960 |
rs46497035 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxl5 | Mm_Celera | 5:43759508 | GTTACAGAGCAAGCC[C/T]AGCAAGCTAGATAAG | 242960 |
rs46639872 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43760481 | CGTAACATCTATAAA[G/T]CCAAGTAAACGCTTA | 242960 |
rs46659466 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Fbxl5 | Mm_Celera | 5:43772011 | ACATATCCCTTAAAC[A/C]CATCCATACGTACGG | 242960 |
rs46662301 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43756839 | CTACGATGAATGCCT[A/G]TCTCAAAACTATTAT | 242960 |
rs46667916 | snp | C/T | 0.231111 | 0.249285 | intron-variant, missense | Fbxl5 | Mm_Celera | 5:43758201 | ACATCCATTTCCTAA[C/T]AACTAGGGCTGATCA | 242960 |
rs46794116 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43757000 | TTACTGCCTCTAACA[C/T]TGTATAACTGGAGCT | 242960 |
rs46805574 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Fbxl5 | Mm_Celera | 5:43756345 | CTCAAATAACAGAAG[C/G]TGGAAGACAAATTTC | 242960 |
rs46812956 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fbxl5 | Mm_Celera | 5:43763341 | ATAGGTACAATTTTT[A/T]AAATTACTAGAAATA | 242960 |
rs46824784 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43748966 | TCCAATAAGTTTAAA[A/G]ACACTTAAGTACAAA | 242960 |
rs46825106 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fbxl5 | Mm_Celera | 5:43761026 | CAAAGAACTGTAAAA[C/T]TCATTCAAGAGAAGG | 242960 |
rs46895016 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Fbxl5 | Mm_Celera | 5:43763307 | TAATGTGATTTTTAA[A/G]AAGTAATTATCAGTA | 242960 |
rs46988047 | snp | A/G | | | intron-variant | Fbxl5 | Mm_Celera | 5:43780232 | CTTGAAAAACCAAAA[A/G]AAAAAAGAAAAAGAA | 242960 |
rs47015847 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxl5 | Mm_Celera | 5:43774375 | AAAGTAAGCCAAGCA[C/T]ATTGAGATAACTTTA | 242960 |
rs47029164 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Fbxl5 | GRCm38.p3 | 5:43761875 | ATACCCAAATGGGTC[C/G]TCTCCAATTCACAAC | 242960 |
rs47352752 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Fbxl5 | Mm_Celera | 5:43746304 | ACTGCCCTTCAGTGC[G/T]TCCCAGCTTAACTGA | 242960 |
rs47373420 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43747689 | AGTCAAACAATTATT[C/T]TGTATCAGGCTAAAT | 242960 |
rs47412546 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fbxl5 | Mm_Celera | 5:43767734 | CCTGTCACTATAATC[A/G]AAGGAGCTCAGAAAA | 242960 |
rs47441335 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43751035 | AAACACTGCGACAGT[C/T]AAGAAACAGGAACCT | 242960 |
rs47526292 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43768495 | TTAGTTATTATTAGA[A/C]ATTTAGCCCAGTACC | 242960 |
rs47780542 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fbxl5 | Mm_Celera | 5:43746633 | GACTGACATGTCTGG[A/G]ATTAGCTTCAAATAA | 242960 |
rs47812019 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fbxl5 | Mm_Celera | 5:43755248 | GTGCCTTTGAGCAGC[C/T]AAGTATGGCCTATGA | 242960 |
rs47880252 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl5 | Mm_Celera | 5:43771365 | ATTTCTAAAGGCAAG[A/G]AATTCACACTTTAAT | 242960 |
rs47921889 | snp | C/G | 0.408163 | 0.193609 | downstream-variant-500B | Fbxl5 | Mm_Celera | 5:43744340 | TCAGACACTGAGCAG[C/G]CCCACTAGCCTGAGA | 242960 |
rs47985031 | snp | A/T | | | intron-variant | Fbxl5 | Mm_Celera | 5:43751721 | TCCCCTAAGGACAGG[A/T]AGCACTCTAGGGAGG | 242960 |
rs48010911 | snp | A/T | 0.132653 | 0.220748 | intron-variant, utr-variant-3-prime | Fbxl5 | Mm_Celera | 5:43757923 | AAATTTACTTCTGTA[A/T]CATATCCTTGAGATT | 242960 |
rs48012162 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43762219 | AGTAGGGATGAATTT[G/T]TACCCACTCTCAGAC | 242960 |
rs48024172 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon | Fbxl5 | Mm_Celera | 5:43759760 | GTCAAATGCAGAATC[A/G]GAAATGTCGGTCTGG | 242960 |
rs48050204 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43751037 | ACACTGCGACAGTCA[A/G]GAAACAGGAACCTTG | 242960 |
rs48127292 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl5 | Mm_Celera | 5:43769497 | CACAGGCTACATACT[A/T]CAATGTAAAGAATAA | 242960 |
rs48270943 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43771226 | CTCCCTACTAACTCC[A/G]ATTCTGGTTTTTAAA | 242960 |
rs48304939 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Fbxl5 | Mm_Celera | 5:43749667 | AAGAGAAATCTAATT[G/T]CCAAGCAACAGAAAA | 242960 |
rs48331666 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43760291 | CCTGGGCCCATATTT[A/C]TAGTAATCTTCTTAA | 242960 |
rs48352028 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl5 | Mm_Celera | 5:43765730 | CGACAATAATGAACA[C/G]AGAACTGACTTCCTC | 242960 |
rs48373739 | snp | C/T | | | intron-variant | Fbxl5 | Mm_Celera | 5:43751592 | CCAGACTCACAATAA[C/T]TCTTAAGGTCTGACT | 242960 |
rs48408568 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43762813 | TATTCCAAGCGTGAA[A/G]TACCAGATTCATCTA | 242960 |
rs48432605 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43748202 | ATGTGTGTTTGGCAT[A/C]GGCGCTTAGTACAGC | 242960 |
rs48472926 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl5 | GRCm38.p3 | 5:43765573 | AATCACGAGTAAAAG[C/T]CAGTGCCTGAAGTCG | 242960 |
rs48491595 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Fbxl5 | Mm_Celera | 5:43759301 | CCTTTGAAATAGGAT[A/C]TATCAGAACTGTGAA | 242960 |
rs48502322 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43748549 | ATGTCAGTGGTGTCA[C/G]CAGTGGGTACAATTC | 242960 |
rs48540673 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fbxl5 | Mm_Celera | 5:43746243 | CAAAATGAGAAGACA[C/T]GGAGCAGGCATCACT | 242960 |
rs48636823 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Fbxl5 | Mm_Celera | 5:43747508 | CAGTCAAAGCCAGAC[A/G]CATCAAAGAAAAGTG | 242960 |
rs48777972 | snp | C/T | 0.336735 | 0.234472 | intron-variant, utr-variant-3-prime | Fbxl5 | Mm_Celera | 5:43757897 | ACATGGTTGACAAAG[C/T]CCTCAATATAAAATT | 242960 |
rs48834222 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl5 | Mm_Celera | 5:43766582 | AACAGGCTTTGGCAT[A/G]GTCTCCAGGGCACAA | 242960 |
rs48879233 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Fbxl5 | Mm_Celera | 5:43766077 | TTCTGTTATTATGTA[C/T]TGTAGAAAGATTCAA | 242960 |
rs48916244 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Fbxl5 | Mm_Celera | 5:43750893 | GTAGTAAAAGTATTC[A/G]TCATTTAGGGAAGGA | 242960 |
rs48958948 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl5 | Mm_Celera | 5:43763228 | TCTGCTGTATACCTG[A/C]CATGTATCTGTGTTA | 242960 |
rs48969386 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43756397 | GTCACTAATATTGCA[C/T]GGTCATTTCTATTTA | 242960 |
rs49006658 | snp | A/C/T | 0.231111 | 0.249285 | intron-variant | Fbxl5 | GRCm38.p3 | 5:43762515 | GATGAACTGATTAAC[A/C/T]GAAATACTCCTAATC | 242960 |
rs49025722 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl5 | Mm_Celera | 5:43764046 | CATATTTACCATGCA[C/G]TGGCTTCATGAAATA | 242960 |
rs49072723 | snp | C/G | 0.32 | 0.24 | intron-variant | Fbxl5 | Mm_Celera | 5:43768971 | AGAACCCTAACAATC[C/G]CAGCTCAGTCGATAT | 242960 |
rs49078465 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43759640 | TTAGTAACAATACAG[A/G]GTAGGATTAGTAAAC | 242960 |
rs49092603 | snp | A/G | 0.231111 | 0.249285 | missense | Fbxl5 | Mm_Celera | 5:43758747 | AAACAGGCATACTGC[A/G]TGGTGGATGGCATGG | 242960 |
rs49140144 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl5 | Mm_Celera | 5:43763406 | GGGTCCAGAAATAGC[C/T]CCATTCTGAGAACAG | 242960 |
rs49235861 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43765716 | TTCATCAGTGGGAGC[A/G]ACAATAATGAACACA | 242960 |
rs49243191 | snp | A/T | 0.408163 | 0.193609 | downstream-variant-500B | Fbxl5 | Mm_Celera | 5:43744189 | ATTCACTCCTCAAAC[A/T]GAAAATACCTGACAG | 242960 |
rs49353965 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Fbxl5 | Mm_Celera | 5:43755036 | TTCTAAAAGATATGT[A/C]ACATTAGAAAAAATA | 242960 |
rs49358180 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43770138 | GTGATATGCTAATGC[A/T]TGTATGTGAGGCACA | 242960 |
rs49415182 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fbxl5 | Mm_Celera | 5:43750155 | AAGGCTGTCCTGGGA[C/T]TACTGACAGTACCTC | 242960 |
rs49463886 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43759556 | ATGATGTTCTGGATC[A/G]GCTGCCACATGTGAA | 242960 |
rs49483673 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Fbxl5 | Mm_Celera | 5:43755321 | AAGCAGGTCTGGGAA[A/G]CAAGTACACAGCTTT | 242960 |
rs49485158 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43749689 | AACAGAAAACTTGCT[A/G]ACTTCTCTGCATTCT | 242960 |
rs49520831 | snp | A/T | 0.132653 | 0.220748 | utr-variant-3-prime | Fbxl5 | Mm_Celera | 5:43744748 | TACAGCAAACAACAG[A/T]CTGCTGCACCAAGAG | 242960 |
rs49561202 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Fbxl5 | Mm_Celera | 5:43746393 | TGCTAACACCCAGAG[A/T]CAGTAATTAGGATAC | 242960 |
rs49831777 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl5 | Mm_Celera | 5:43765704 | CCCAGATCATACTTC[A/C]TCAGTGGGAGCGACA | 242960 |
rs49876482 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43760979 | TTTGTAAACAATTCA[A/C]TTTCCAGCAACAAGA | 242960 |
rs49977742 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43750571 | ACATCCTAGAATAAT[C/T]TCCGTGTTTCTATAA | 242960 |
rs49977900 | snp | A/C | 0.408163 | 0.193609 | utr-variant-3-prime | Fbxl5 | GRCm38.p3 | 5:43744693 | TTTAAAAATCCTTCT[A/C]GAATTCAACAGTTTA | 242960 |
rs50012387 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43766579 | CTTAACAGGCTTTGG[C/G]ATGGTCTCCAGGGCA | 242960 |
rs50023244 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43767876 | AACCCAACCCTAGAT[C/T]GAAGAATATTGCAAA | 242960 |
rs50035113 | snp | A/T | 0.408163 | 0.193609 | utr-variant-3-prime | Fbxl5 | Mm_Celera | 5:43744822 | GTTTGAATTGGCCCC[A/T]CAGAATTGTTCAAAT | 242960 |
rs50059324 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43755850 | TGTCAAGCTACTGGG[A/G]TTAGGTGTCAGCTGC | 242960 |
rs50065045 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Fbxl5 | Mm_Celera | 5:43758377 | ACACATTGCAGAAGT[C/T]GCTGGGAGTGTAGTC | 242960 |
rs50068617 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Fbxl5 | Mm_Celera | 5:43745947 | AAACCACTTATGGAA[C/T]AATTGGAATTTTACA | 242960 |
rs50114349 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43759438 | GGAGCTCTGTGAAAA[A/G]GCACTTAAAATCTGG | 242960 |
rs50126070 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fbxl5 | Mm_Celera | 5:43762727 | CTTTAGAAATCATAA[A/G]ATACATGAACTTTAA | 242960 |
rs50150114 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl5 | Mm_Celera | 5:43755112 | TTTGGTGCATGACTC[A/G]TGTGTGGTGGTGTGA | 242960 |
rs50219567 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43763271 | GTTATAAAAAGCATA[C/G]TATAATGAGGTTTCT | 242960 |
rs50259926 | snp | A/C | 0.132653 | 0.220748 | missense | Fbxl5 | Mm_Celera | 5:43760802 | TTAAGCCATGGAGTA[A/C]ACGTTTTTCCATTTG | 242960 |
rs50317951 | snp | G/T | | | intron-variant | Fbxl5 | Mm_Celera | 5:43752621 | CCCAAGCCTCCTATG[G/T]GCTAGAATTAACTGG | 242960 |
rs50369039 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Fbxl5 | Mm_Celera | 5:43774216 | AAGAAAACTGACATA[A/T]TATAAAGTGTGCCAT | 242960 |
rs50390451 | snp | C/G | 0.336735 | 0.234472 | intron-variant, utr-variant-3-prime | Fbxl5 | Mm_Celera | 5:43758178 | AATGTAATATTTCAT[C/G]TGCAAATACATCCAT | 242960 |
rs50391878 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl5 | Mm_Celera | 5:43763375 | TAATCTTTTTTCCCT[A/G]CTGTGACTTCACTTT | 242960 |
rs50469498 | snp | A/G | 0.408163 | 0.193609 | utr-variant-3-prime | Fbxl5 | GRCm38.p3 | 5:43744847 | TCAAATAAAGAAAAC[A/G]TTAGGGGAAAAGAGA | 242960 |
rs50508550 | snp | C/G | | | intron-variant | Fbxl5 | Mm_Celera | 5:43780130 | CCAGGACTTATGAGG[C/G]AGAAGCAGGCGGATT | 242960 |
rs50581167 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl5 | Mm_Celera | 5:43765773 | CATAGACAGAACAAT[A/C]CTCACTTTGTAGCAT | 242960 |