SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13464870 | snp | G/T | 0.244898 | 0.249948 | utr-variant-3-prime | Ubxn4 | Mm_Celera | 1:128278914 | CTGGAAAAACATTAA[G/T]TACCTCAAGTCAATT | 67812 |
rs13464871 | snp | C/T | 0.475309 | 0.108333 | utr-variant-3-prime | Ubxn4 | GRCm38.p3 | 1:128279003 | AGGATCACTCTTCAA[C/T]GTTATCTCTTTTAAA | 67812 |
rs13464872 | snp | G/T | | | utr-variant-3-prime | Ubxn4 | Mm_Celera | 1:128277656 | TATCGAGGTCACTTT[G/T]GTCTGACTTTTTCCT | 67812 |
rs13464873 | snp | C/T | 0.426035 | 0.177515 | missense | Ubxn4 | GRCm38.p3 | 1:128258983 | CAGCTACCTCTGACA[C/T]AAAGTCAGATACTGC | 67812 |
rs30528197 | snp | A/G | 0.5 | 0 | intron-variant | Ubxn4 | GRCm38.p3 | 1:128250857 | AAGTATTGTAGGCAT[A/G]TGTGTATGCTCACTA | 67812 |
rs30567088 | snp | A/G | 0.5 | 0 | intron-variant | Ubxn4 | GRCm38.p3 | 1:128257325 | TATGTTGATCTGCAG[A/G]AAATCTGCTCAATAT | 67812 |
rs30699036 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ubxn4 | Mm_Celera | 1:128272439 | TTCCAGAGGTCCTGA[C/G]TTCAATTCCCAGCAA | 67812 |
rs30944763 | snp | A/T | 0.5 | 0 | intron-variant | Ubxn4 | Mm_Celera | 1:128251152 | GCAACTTTTTTTTTT[A/T]AAGTGTTAAGTGGTG | 67812 |
rs31819183 | snp | C/T | 0.5 | 0 | intron-variant | Ubxn4 | GRCm38.p3 | 1:128275113 | CCCATTCACTGAACA[C/T]TCTTTATTCCATAAT | 67812 |
rs31888985 | snp | A/T | 0.5 | 0 | intron-variant | Ubxn4 | Mm_Celera | 1:128268264 | CAGGGCTACACAGAG[A/T]AACCCTGTCTCGGAA | 67812 |
rs31908780 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ubxn4 | Mm_Celera | 1:128262582 | TGGTTGCTGGGATTT[C/G]AACTCTGGACCTTCG | 67812 |
rs32345531 | snp | A/T | 0.5 | 0 | intron-variant | Ubxn4 | Mm_Celera | 1:128271901 | TAAATAGCTCAGCTG[A/T]TTTTATTTTGACCAC | 67812 |
rs32523294 | snp | A/C | 0.5 | 0 | intron-variant | Ubxn4 | Mm_Celera | 1:128268005 | CAAGAGCAATGGGTT[A/C]TCTTAACTGCTGAGC | 67812 |
rs32556878 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ubxn4 | GRCm38.p3 | 1:128275692 | CTTGAACTTCTTGCC[A/T]CTTCTTTCCAAGTGC | 67812 |
rs32610615 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubxn4 | Mm_Celera | 1:128248242 | GCACGCCTTTAATCC[C/T]AGCACTCAGGAGGCA | 67812 |
rs32654145 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Ubxn4 | GRCm38.p3 | 1:128270563 | AGTAGTCTTCTCATC[A/G]CGTCTTCTCATCACA | 67812 |
rs32686918 | snp | A/G | 0.48 | 0.0979796 | intron-variant, downstream-variant-500B | Ubxn4, LOC105246702 | Mm_Celera | 1:128245792 | TAAATTAATAAATTA[A/G]TCTTGTAATCCAGTA | 67812 |
rs32703580 | snp | C/T | 0.387812 | 0.208586 | utr-variant-5-prime, upstream-variant-2KB | Ubxn4, LOC105246702 | Mm_Celera | 1:128244326 | GGGGTGGCTGTCGGG[C/T]GTACGGGCTGGCTGG | 67812 |
rs32769789 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubxn4 | GRCm38.p3 | 1:128246217 | CAAGTGTTGTGATTA[C/T]AGACGTGTGCAACAC | 67812 |
rs45643997 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubxn4 | Mm_Celera | 1:128249806 | TAAGGGAATGAGAGC[A/G]CCAACCTCACAAAAG | 67812 |
rs45698471 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Ubxn4 | GRCm38.p3 | 1:128255873 | AAATAGGTGACAAAA[A/C/G]GCAGATGAATATAAG | 67812 |
rs45763446 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ubxn4 | Mm_Celera | 1:128247798 | ATAGCTTTTCTAGAG[C/T]TTTAGCTAGGTCATC | 67812 |
rs45813330 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Ubxn4 | Mm_Celera | 1:128270669 | AGGCTTGCTTTACTA[C/G]AACTGCTGCAAGTAC | 67812 |
rs45816285 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ubxn4 | Mm_Celera | 1:128269990 | AGTTTATAAAGATGG[C/T]TGTGTGGGTTAGTGA | 67812 |
rs45908425 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB, utr-variant-5-prime | Ubxn4, LOC105246702 | Mm_Celera | 1:128244026 | ACTCTCGCCATGCTT[C/T]GAGCCCACAGTTTAC | 67812 |
rs45926519 | snp | C/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Ubxn4, LOC105246702 | Mm_Celera | 1:128245013 | CCCAGCCCTGGTGTT[C/T]CCCTTCTTGGTCCTC | 67812 |
rs45968969 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Ubxn4 | Mm_Celera | 1:128277771 | TACTGATGCATCTGT[C/T]TTATAACCTGTTCTC | 67812 |
rs46129089 | snp | C/T | 0.124444 | 0.216185 | missense | Ubxn4 | Mm_Celera | 1:128269912 | CCTGATGGTTCTTCC[C/T]TTACAAACCAGTTTC | 67812 |
rs46341163 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ubxn4 | Mm_Celera | 1:128261431 | TTTTCCTCTGTGCAG[C/T]GAGTCTTTCATACTA | 67812 |
rs46408578 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubxn4 | Mm_Celera | 1:128274669 | GGCACTTGGGAAGAC[A/G]TAAAAGGTGATCATT | 67812 |
rs46410618 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB | Ubxn4 | Mm_Celera | 1:128242558 | TGTAAAGCACTTAAT[G/T]GCTACATAAGTAACA | 67812 |
rs46689095 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ubxn4 | Mm_Celera | 1:128260192 | AGCTTTGCAAAAACA[G/T]TAATAATGACAGTAA | 67812 |
rs46881181 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Ubxn4 | Mm_Celera | 1:128265994 | GAAAAAAATCTCAGA[G/T]CCAAGCCGGGCAGTG | 67812 |
rs46892951 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ubxn4 | Mm_Celera | 1:128256079 | TTTTATAAAACTTCT[A/T]GTTTCAAGCGTGAAT | 67812 |
rs47147004 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ubxn4 | Mm_Celera | 1:128272114 | GAAGAAAAGGAGAGT[A/G]TGGAATTTAAACTAT | 67812 |
rs47151787 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ubxn4 | Mm_Celera | 1:128270194 | GAATGAGAAGCAAGC[A/G]GTCTCCTAGATGTCA | 67812 |
rs47207010 | snp | C/T | | | intron-variant | Ubxn4 | Mm_Celera | 1:128251936 | CAGAGGACCAGTTTT[C/T]TTCCCATCATCCACA | 67812 |
rs47221025 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Ubxn4, LOC105246702 | Mm_Celera | 1:128243484 | AGCATAGCATAGTGG[C/T]TGAAGGTTTTACAAT | 67812 |
rs47302363 | snp | C/T | 0.336735 | 0.234472 | utr-variant-5-prime, upstream-variant-2KB | Ubxn4, LOC105246702 | Mm_Celera | 1:128244315 | CGCGTCCCCAGGGGG[C/T]GGCTGTCGGGCGTAC | 67812 |
rs47310447 | snp | A/G | 0.124444 | 0.216185 | missense | Ubxn4 | Mm_Celera | 1:128258853 | TCGTCAAAAGGTGAA[A/G]CATCAGTGACAAATG | 67812 |
rs47393488 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Ubxn4 | Mm_Celera | 1:128271703 | CGTGATGGTTTGTGT[A/T]CTTGGATCACTGTAT | 67812 |
rs47477329 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ubxn4 | GRCm38.p3 | 1:128255841 | TCTGAAGAACAGTAT[A/G]GAGTAGTTTACTGTT | 67812 |
rs47491672 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubxn4 | Mm_Celera | 1:128257857 | GTCCATAAGGTTCTT[C/T]CCTCTTGCTCTCCAC | 67812 |
rs47511553 | snp | C/T | | | intron-variant | Ubxn4 | Mm_Celera | 1:128274222 | CACACCAGAAAAGAA[C/T]ATCAGATCTCATTAC | 67812 |
rs47535515 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ubxn4 | Mm_Celera | 1:128255334 | TAAGGGGAAAAAAAG[C/T]ACTTATATTGGTATA | 67812 |
rs47556892 | snp | A/C | 0.231111 | 0.249285 | utr-variant-3-prime | Ubxn4 | Mm_Celera | 1:128278466 | ACACGCTAATGATGT[A/C]TGTCCTTGGAGTTCT | 67812 |
rs47573013 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ubxn4 | Mm_Celera | 1:128276635 | AAATTATATCTAGTA[C/T]GTGTCTCGGCTTGTA | 67812 |
rs47584313 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Ubxn4 | Mm_Celera | 1:128277062 | TGAAGACGAGAACAA[C/T]ACTTGGAATGGAAAC | 67812 |
rs47687776 | snp | A/G | 0.132653 | 0.220748 | intron-variant, downstream-variant-500B | Ubxn4, LOC105246702 | Mm_Celera | 1:128245736 | TGCTGTTAATTAGAA[A/G]AGCATAAATTACTTA | 67812 |
rs47822786 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB | Ubxn4, LOC105246702 | Mm_Celera | 1:128242715 | AGGTGCTCACGAACT[G/T]GGGTAGCTGTTTCCA | 67812 |
rs47826458 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ubxn4 | Mm_Celera | 1:128276894 | ATATCAGAAGAAATG[A/T]GAGAAACAGCTTTGC | 67812 |
rs47979345 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ubxn4 | Mm_Celera | 1:128250551 | AACAAAAAAACTGAA[A/T]TAGAATAAAATAGTG | 67812 |
rs47987611 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubxn4 | Mm_Celera | 1:128259100 | GCCTGTTCAAATGGC[C/T]TGATAAACCCAACCT | 67812 |
rs47990955 | snp | C/G | 0.32 | 0.24 | intron-variant | Ubxn4 | Mm_Celera | 1:128254213 | GTGTACAGGTAATTC[C/G]TAGTCACTATCTTTT | 67812 |
rs47996913 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Ubxn4 | Mm_Celera | 1:128278503 | GTCTTCTGCATTGAT[C/T]ACATTTGTTAACACT | 67812 |
rs48038531 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ubxn4 | Mm_Celera | 1:128260624 | GACAGATAAACCCGC[A/T]GTGCTTTCAGAGGAT | 67812 |
rs48071245 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Ubxn4, LOC105246702 | Mm_Celera | 1:128244612 | TCTGGATTCTCGTTA[A/G]CGTCGAGTGAGCTAG | 67812 |
rs48123995 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Ubxn4 | Mm_Celera | 1:128277227 | AGAGGTTTTGAGTTA[A/G]GTTGTTTAACCTGAA | 67812 |
rs48129488 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime | Ubxn4 | Mm_Celera | 1:128277424 | CACACACAGTAACTG[C/G]TATGTCACTGAGTAG | 67812 |
rs48148598 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, utr-variant-5-prime | Ubxn4, LOC105246702 | Mm_Celera | 1:128243980 | GATACCTAGCATTTA[C/T]TCTTACAGCGTTGAT | 67812 |
rs48153328 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ubxn4, LOC105246702 | Mm_Celera | 1:128244707 | CTCTTCGGGGCCGCT[A/C]GTCTCCTGTCCGGGC | 67812 |
rs48176625 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Ubxn4, LOC105246702 | Mm_Celera | 1:128242771 | ATTAGTCACTTGTAT[C/T]TGCCTTCGAAGCAGA | 67812 |
rs48268602 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ubxn4 | GRCm38.p3 | 1:128247338 | TGGTAAAATAAGTCA[A/G]TAAAGAAATGAGAAT | 67812 |
rs48281762 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Ubxn4 | Mm_Celera | 1:128278991 | TGTGTGAGTAACAGG[A/G]TCACTCTTCAACGTT | 67812 |
rs48365712 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubxn4 | Mm_Celera | 1:128250735 | ACATTCGTTCAGAAT[C/T]GTCTCACTTCCAAAT | 67812 |
rs48368853 | snp | A/G | | | intron-variant | Ubxn4 | Mm_Celera | 1:128252029 | CACTGCACACATGTG[A/G]TGCTGTTAAATTACA | 67812 |
rs48383433 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Ubxn4 | Mm_Celera | 1:128278283 | AATGCCTTCTGTGGA[C/T]GTAATTCCTGTTGAG | 67812 |
rs48479743 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime | Ubxn4 | Mm_Celera | 1:128277274 | TAGCTGGATGCTAGG[A/T]CCTTGTGTAGGGTAA | 67812 |
rs48509412 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubxn4 | Mm_Celera | 1:128273610 | GATTTCATGGTGTTC[A/G]CCAGATTTTATTACC | 67812 |
rs48961743 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubxn4 | Mm_Celera | 1:128252136 | GTTCTAGTTTCACAC[A/G]GGAAAGAATTTAGAA | 67812 |
rs49057003 | snp | C/T | | | synonymous-codon | Ubxn4 | Mm_Celera | 1:128269935 | CCAGTTTCCTTCTGA[C/T]GCTCCTCTAGAAGAA | 67812 |
rs49060993 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Ubxn4 | Mm_Celera | 1:128249888 | CGTTTGTTATTCTCC[A/C]AAAGGGTTTCTGGCT | 67812 |
rs49127454 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Ubxn4 | Mm_Celera | 1:128252361 | GATTTTTGTTGTTGT[A/T]GTTACCTATGATAAT | 67812 |
rs49142886 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ubxn4 | Mm_Celera | 1:128270336 | TGCTCAAAAATCTAA[C/G]TGACGTGAAATTTGA | 67812 |
rs49174379 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Ubxn4 | Mm_Celera | 1:128279423 | CAAAGACCTCGACCT[A/G]CCTATACACAACTAG | 67812 |
rs49213669 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubxn4 | Mm_Celera | 1:128247743 | AATACTGTTAGGGAT[A/G]GACAGTGGAGTCTGT | 67812 |
rs49225769 | snp | C/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Ubxn4, LOC105246702 | Mm_Celera | 1:128245393 | GTGCCAACTCATTTA[C/T]CCCATATTGCTCTAA | 67812 |
rs49244980 | snp | A/G | | | missense | Ubxn4 | Mm_Celera | 1:128269970 | GGCAGTTTGCTGCAC[A/G]GGTAAGTTTATAAAG | 67812 |
rs49260167 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubxn4 | Mm_Celera | 1:128256000 | TATGGTCGTTGAGGT[A/G]AGAAACTTGCTAGCT | 67812 |
rs49425070 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubxn4 | Mm_Celera | 1:128250063 | GTGGTGAGCTTTTCT[A/G]TATTTAGTGTGGCTC | 67812 |
rs49455105 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Ubxn4, LOC105246702 | Mm_Celera | 1:128243234 | CTTCCATTTTGATTT[C/T]GTATGCATCCATAAA | 67812 |
rs49496054 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Ubxn4 | Mm_Celera | 1:128278852 | CTGTCTCTGCAATAA[C/T]GAGGCAATATATGAG | 67812 |
rs49553522 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubxn4 | Mm_Celera | 1:128250672 | GGTTGATAGTTGACT[C/T]TTTTTCTTGGGAATT | 67812 |
rs49576162 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB | Ubxn4 | Mm_Celera | 1:128242556 | TCTGTAAAGCACTTA[A/C]TTGCTACATAAGTAA | 67812 |
rs49805052 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ubxn4 | Mm_Celera | 1:128254186 | TAATCCTTGTTAGTA[A/C]ATGTTAATCATGTGT | 67812 |
rs49819257 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubxn4 | Mm_Celera | 1:128257615 | ATCCTTTAGAGTGGC[A/G]CCTATGTGAGTGTCA | 67812 |
rs49844888 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Ubxn4 | Mm_Celera | 1:128277462 | CCCGAGCACCTCAGC[A/G]AGCTAATCAGGTGAT | 67812 |
rs49995144 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ubxn4 | Mm_Celera | 1:128270118 | GCTTTCTGGCTTGTA[C/T]TATACGTGATCACAG | 67812 |
rs50064545 | snp | A/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128265980 | AGAAAACAAACAAAG[A/G]AAAAAATCTCAGATC | 67812 |
rs50106503 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ubxn4 | Mm_Celera | 1:128259771 | CTTAGAATCCCTTCT[C/G]GTGCATACATGTGTG | 67812 |
rs50117878 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubxn4 | Mm_Celera | 1:128252193 | TTAAATCCTTGAAAT[A/G]TTTTCACAGGGGATG | 67812 |
rs50119058 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ubxn4 | Mm_Celera | 1:128251701 | ACCATGGGACTACAT[C/T]CATGACTTCAGGAGA | 67812 |
rs50123652 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Ubxn4 | Mm_Celera | 1:128265944 | AATAGTAACTCAGAT[A/T]CTTCACAGTTGCTTA | 67812 |
rs50177853 | snp | A/G | 0.124444 | 0.216185 | utr-variant-5-prime, upstream-variant-2KB | Ubxn4, LOC105246702 | Mm_Celera | 1:128244465 | CGCCTGGGCCTGAAG[A/G]GGACGATGCTGTGGT | 67812 |
rs50179081 | snp | C/T | 0.32 | 0.24 | intron-variant | Ubxn4 | Mm_Celera | 1:128275818 | TGAAAGCTATCACTC[C/T]GCGGTGTGGAGATAC | 67812 |
rs50210611 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubxn4 | Mm_Celera | 1:128273216 | TGTTTCATCTGTAAA[C/T]TGTTAGCCTATGACT | 67812 |
rs50353179 | snp | A/C | | | intron-variant | Ubxn4 | Mm_Celera | 1:128263265 | AGTTTAGAAAAATTA[A/C]CAGATAATCACTTTA | 67812 |
rs50368296 | snp | A/G | 0.336735 | 0.234472 | intron-variant, nc-transcript-variant | Ubxn4, LOC105246702 | Mm_Celera | 1:128245266 | TGAGGTGCAATAATT[A/G]CTTTATTACAAGTTG | 67812 |
rs50463113 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ubxn4 | Mm_Celera | 1:128265940 | GTTTAATAGTAACTC[A/G]GATTCTTCACAGTTG | 67812 |
rs50510308 | snp | A/G | 0.391111 | 0.206368 | downstream-variant-500B | Ubxn4 | Mm_Celera | 1:128279813 | AAAGTTGCATGAATT[A/G]AGACACTCCTCCCTC | 67812 |