SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3670524 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Usp38 | GRCm38.p3 | 8:80997027 | TGCTCCAAAAATAAT[A/G]CTCATTATTAAAATA | 74841 |
rs3671096 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Usp38 | Mm_Celera | 8:80997111 | TACCAACTTTTTTTT[A/T]TAAGCAGTGAATGAA | 74841 |
rs3671098 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Usp38 | Mm_Celera | 8:80997112 | ACCAACTTTTTTTTT[A/T]AAGCAGTGAATGAAG | 74841 |
rs3685869 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Usp38 | Mm_Celera | 8:80997174 | CAGGGAACATCAGAA[A/G]AGTTGTCAAAGAAAG | 74841 |
rs3686494 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Usp38 | Mm_Celera | 8:80997270 | CACCTCAACTAATAG[C/T]GCCTGTAGTTTCCTG | 74841 |
rs3694369 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Usp38 | Mm_Celera | 8:81001408 | ATCATTCAGTTTACT[C/T]GATCAGTATGTACTG | 74841 |
rs3694387 | snp | G/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Usp38 | Mm_Celera | 8:81001418 | TTACTTGATCAGTAT[G/T]TACTGAACACCTACT | 74841 |
rs3695529 | snp | A/G | 0.396694 | 0.202437 | intron-variant, upstream-variant-2KB | Usp38 | Mm_Celera | 8:81001589 | GCCAAGGAGTCTGCC[A/G]TTTTAAAGAGGGTGT | 74841 |
rs3696141 | snp | C/T | 0.396694 | 0.202437 | intron-variant, upstream-variant-2KB | Usp38 | Mm_Celera | 8:81001671 | GCTCCACAGACAGAA[C/T]AAGAGCATTTATGAA | 74841 |
rs3696786 | snp | A/G | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Usp38 | Mm_Celera | 8:81001790 | CGAAAACATCTGGAC[A/G]TAGGATGACAGAAGA | 74841 |
rs3707622 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Usp38, Gm31223 | Mm_Celera | 8:80982607 | AGTTTCCCAGGAAAT[A/C]AATGATGTTTGCCTA | 74841 |
rs3707705 | snp | C/G | 0.30839 | 0.243086 | intron-variant | Usp38, Gm31223 | Mm_Celera | 8:80982654 | CAGATGCTTAATAAA[C/G]ACTAATGCTCTTATT | 74841 |
rs3708211 | snp | A/C | 0.471655 | 0.115624 | intron-variant | Usp38, Gm31223 | Mm_Celera | 8:80982679 | CTTATTTTAGAACAT[A/C]ATTAGTTACTGGGAA | 74841 |
rs3710700 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Usp38, Gm31223 | Mm_Celera | 8:80983080 | CTTCTCATCTGATAA[A/G]CATTGTAACATTGAT | 74841 |
rs4227271 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Usp38 | Mm_Celera | 8:80985197 | GCTTTCACAGTAGTA[C/T]TGGTTCTCCCCAGTA | 74841 |
rs4227272 | snp | A/C | 0.21875 | 0.248039 | missense | Usp38 | Mm_Celera | 8:80985271 | AAGTTGTGCTTTCAC[A/C]TCCTGGGTTCTGAGG | 74841 |
rs4227273 | snp | C/T | 0.444444 | 0.157135 | missense | Usp38 | Mm_Celera | 8:80985309 | TTACTGATGAGAATC[C/T]TTGCAGATTCTTCAG | 74841 |
rs4227274 | snp | A/G | 0.21875 | 0.248039 | synonymous-codon | Usp38 | Mm_Celera | 8:80985398 | ATTCACAACTGAGTC[A/G]CAGACAAAGGCAGCT | 74841 |
rs4227275 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Usp38 | Mm_Celera | 8:80985413 | GCAGACAAAGGCAGC[C/T]GTTGCTGGATTATAA | 74841 |
rs4227276 | snp | C/T | 0.424383 | 0.179139 | synonymous-codon | Usp38 | GRCm38.p3 | 8:80985464 | GTCAGCGACACTGGT[C/T]TGCATTAGCCCATCA | 74841 |
rs4227277 | snp | A/C/T | 0.162571 | 0.245019 | synonymous-codon | Usp38 | Mm_Celera | 8:80985497 | TTGAGCACTGGGTAA[A/C/T]GAAGCTGTATCTTGG | 74841 |
rs4227278 | snp | A/C | 0.21875 | 0.248039 | missense | Usp38 | Mm_Celera | 8:80985508 | GTAACGAAGCTGTAT[A/C]TTGGAAAGACAGGTC | 74841 |
rs4227279 | snp | C/G | 0.21875 | 0.248039 | missense | Usp38 | Mm_Celera | 8:80985512 | CGAAGCTGTATCTTG[C/G]AAAGACAGGTCTTCC | 74841 |
rs4227280 | snp | A/G | 0.252401 | 0.249988 | synonymous-codon | Usp38 | Mm_Celera | 8:80985596 | GTGTGAGGTACTCCC[A/G]CAGTTTAGGCAGCAG | 74841 |
rs6342939 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Usp38 | Mm_Celera | 8:80995583 | TTAATGAAACTACCA[C/T]CTTAAAAACAGCTCA | 74841 |
rs13461492 | snp | A/G | 0.188366 | 0.242283 | missense, downstream-variant-500B | Usp38, Gm31223 | GRCm38.p3 | 8:80984538 | GAGCTAATGGCATAG[A/G]CAGTGACAATCCAGC | 74841 |
rs13461493 | snp | C/G | 0.197531 | 0.244432 | synonymous-codon | Usp38 | Mm_Celera | 8:80984993 | CTTCTCTTCCTTGTC[C/G]CAGAGTTGGTCTGTA | 74841 |
rs13461494 | snp | C/T | 0.207612 | 0.24638 | missense, downstream-variant-500B | Usp38, Gm31223 | GRCm38.p3 | 8:80984508 | CCAGTGGTGTCTGGG[C/T]CAATGGAGATCCACC | 74841 |
rs13461495 | snp | C/T | 0.290657 | 0.246672 | utr-variant-3-prime, intron-variant | Usp38, Gm31223 | GRCm38.p3 | 8:80981686 | TACTTTAAGAAAATA[C/T]ACTCAGTGGTTGTTT | 74841 |
rs13461496 | snp | G/T | | | missense | Usp38 | Mm_Celera | 8:80985399 | CAGCTGCCTTTGTCT[G/T]CGACTCAGTTGTGAA | 74841 |
rs13461497 | snp | A/G/T | 0.336735 | 0.234472 | synonymous-codon, downstream-variant-500B | Usp38, Gm31223 | GRCm38.p3 | 8:80984873 | CTACCTATTAAGTTC[A/G/T]GTTGTTGTGCACTCT | 74841 |
rs13461498 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime, intron-variant | Usp38, Gm31223 | GRCm38.p3 | 8:80981604 | CTCATTTGCAGTTAC[A/G]GTTAGACATGTTTGG | 74841 |
rs32539171 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Usp38 | Mm_Celera | 8:80996512 | CTCTGTATGTATTAT[A/G]CACACAATCCACCTA | 74841 |
rs32558048 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Usp38 | Mm_Celera | 8:80992390 | CACTATTTAAGGAAA[A/C]GTTGACAATTATTTT | 74841 |
rs32599079 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Usp38 | Mm_Celera | 8:81016526 | TACGAAGAGACCAGT[A/G]TCACTGAAGTGAAAT | 74841 |
rs32604631 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Usp38 | Mm_Celera | 8:81003430 | TCCATTGTTGGTGGG[A/C]TTGCAGGCTTGTACA | 74841 |
rs32612945 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Usp38 | Mm_Celera | 8:81015208 | GGGAGCCTACTCTGA[A/G]TTCTGAGGTTCTTGT | 74841 |
rs32635690 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Usp38 | Mm_Celera | 8:80992822 | GAATTAAAAAAAAAT[A/T]CAGTAGGACAGTAGA | 74841 |
rs32648799 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Usp38, Gm31223 | GRCm38.p3 | 8:80981221 | ACACAAGGTGCATGA[C/T]GCCAGAGGGCAGGGG | 74841 |
rs32665649 | snp | C/G | 0.32 | 0.24 | intron-variant | Usp38 | Mm_Celera | 8:80992992 | AAGTACAATGTACAA[C/G]CTAATTCGATCCAGA | 74841 |
rs32667799 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Usp38 | Mm_Celera | 8:81015146 | CACTCTCACGTCACT[A/G]GAGACTGTGTGGTAC | 74841 |
rs32669317 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp38 | Mm_Celera | 8:80994525 | GATCCAGATGTAGAA[C/T]TCCCAGCTCCTTTTC | 74841 |
rs32671285 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Usp38 | Mm_Celera | 8:81000120 | AAATATCCTGTACGT[A/G]ATGATGTCACAAGAC | 74841 |
rs32688377 | snp | A/G | 0.265928 | 0.249492 | synonymous-codon, nc-transcript-variant | Usp38 | Mm_Celera | 8:80995727 | ATCTGGGAATCCGGA[A/G]TAATGGTACATCATA | 74841 |
rs32691373 | snp | A/G | 0.18 | 0.24 | intron-variant | Usp38 | Mm_Celera | 8:80994935 | ATGCTTCTGTGTACC[A/G]TTTACTTCTGAAAGG | 74841 |
rs32704920 | snp | A/G | 0.396694 | 0.202437 | intron-variant, nc-transcript-variant | Usp38, Gm31223 | GRCm38.p3 | 8:80983335 | CAAAATAATTAGAAT[A/G]TTAGAACTAGACTGA | 74841 |
rs32706153 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Usp38 | Mm_Celera | 8:81001960 | CATTTAAAGTTAGTA[A/G]ATTTTATAGGACAGA | 74841 |
rs32708494 | snp | A/T | 0.375 | 0.216506 | intron-variant | Usp38 | GRCm38.p3 | 8:80991797 | ACCCAGCACTAACAA[A/T]CACATTTAAAGAAAA | 74841 |
rs32711877 | snp | A/C | 0.375 | 0.216506 | utr-variant-5-prime, nc-transcript-variant | Usp38 | Mm_Celera | 8:81014689 | CCGGAGGTCCGCATA[A/C]GGCTGCCTCGCTGGG | 74841 |
rs32712460 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB | Usp38 | Mm_Celera | 8:81015519 | AGTTGGGGTACAGGA[C/G]TTTTCACTTTCATCA | 74841 |
rs32719356 | snp | G/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B, nc-transcript-variant | Usp38, Gm31223 | GRCm38.p3 | 8:80980653 | TTTAGGTGTTTAGGT[G/T]GGTGTTTTTTGCACG | 74841 |
rs32725355 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Usp38 | Mm_Celera | 8:80993818 | TGAGTCACTTATCAC[A/G]GCATCCACAAAATAG | 74841 |
rs32729998 | snp | A/G | 0.265928 | 0.249492 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Usp38 | Mm_Celera | 8:81001068 | CACATGGAATGCCTC[A/G]GGAGAATGCTGAAAA | 74841 |
rs32733256 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Usp38 | Mm_Celera | 8:80995642 | TTTGTTCCTTATATC[A/G]TATGTTGCTCACCAA | 74841 |
rs32762137 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Usp38 | Mm_Celera | 8:80992378 | CAGCTCAATTGGCAC[G/T]ATTTAAGGAAACGTT | 74841 |
rs32769021 | snp | G/T | 0.387812 | 0.208586 | downstream-variant-500B, nc-transcript-variant, intron-variant | Usp38, Gm31223 | GRCm38.p3 | 8:80980227 | CAGTCTTGAGGGTGC[G/T]TTCCTGAGTTACCCT | 74841 |
rs32776510 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp38 | Mm_Celera | 8:80998302 | CTTTCATGCCCTACC[C/T]TCTCTCTATATTTTA | 74841 |
rs32779668 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp38 | Mm_Celera | 8:81007883 | GGAGTAATGTACACT[C/T]ACAATGTGTCTTTAC | 74841 |
rs32780732 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp38 | Mm_Celera | 8:80998073 | TGCCATCTTTTAAGA[C/T]CTGAATTCTATGACA | 74841 |
rs32781423 | snp | C/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Usp38 | Mm_Celera | 8:81002850 | TTCCTAACCGCTGAG[C/G]CACCTCTCCAGCACC | 74841 |
rs32793953 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp38 | GRCm38.p3 | 8:80986013 | CAGCTTGGTGTGCGC[A/G]CTGTATAACAGCGCA | 74841 |
rs32805497 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp38 | Mm_Celera | 8:81003328 | ACTTGCAGTAAGTTT[A/G]GATTAAGAAGAAAGT | 74841 |
rs32809234 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp38 | Mm_Celera | 8:80995025 | GTTTCAGTTAGCTGA[A/G]CAGATGCAAAAACAG | 74841 |
rs32812139 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Usp38 | Mm_Celera | 8:81016393 | GGAGGTGGGAGGACA[C/T]ATTCCAGCTTCAGCA | 74841 |
rs32818155 | snp | C/T | 0.5 | 0 | intron-variant | Usp38 | Mm_Celera | 8:81012452 | ATCATGGGTATACTC[C/T]AAATCGAAAGTTAAA | 74841 |
rs32824372 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp38 | Mm_Celera | 8:81005582 | GTATTTACTACTGAG[C/T]TTCTAGTAAAAAGAA | 74841 |
rs32830011 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp38 | Mm_Celera | 8:80997496 | AGAGTGAAAGTCACT[C/G]TACTTTGGGGACATG | 74841 |
rs32830812 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp38 | Mm_Celera | 8:81009506 | CTTGGAATATATTTA[C/T]ATATGACTAACCAGA | 74841 |
rs32832030 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Usp38 | Mm_Celera | 8:81016525 | TTACGAAGAGACCAG[C/T]ATCACTGAAGTGAAA | 74841 |
rs32835538 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp38 | Mm_Celera | 8:80998485 | GCAGATCCACAGGCA[C/T]AGTAGCCAAGCTCTT | 74841 |
rs32842357 | snp | A/G | 0.265928 | 0.249492 | intron-variant, utr-variant-5-prime | Usp38 | Mm_Celera | 8:81000786 | GGTTTCTACACTGCT[A/G]CTGTGTAAAGGTACC | 74841 |
rs32854106 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp38 | Mm_Celera | 8:81006743 | TAACTGCTGTTATCT[A/G]GGTGCCCTCCATCTT | 74841 |
rs32869644 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp38 | Mm_Celera | 8:81003500 | GGACATAGTACTACC[A/G]GAGGATCCAGCAATA | 74841 |
rs32878283 | snp | A/C | 0.255 | 0.24995 | intron-variant | Usp38 | Mm_Celera | 8:80997894 | TGCATAATATCTTTG[A/C]AGCTCCAAATCCTGT | 74841 |
rs32879603 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp38 | Mm_Celera | 8:81008364 | TATGGACCGATATGC[C/G]TTCTGCCTGTGATTT | 74841 |
rs32887112 | snp | C/T | 0.32 | 0.24 | utr-variant-5-prime, nc-transcript-variant | Usp38 | Mm_Celera | 8:81014857 | AGGAGGCGCTGTCAA[C/T]GCGAGTACCTCGATC | 74841 |
rs32888321 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp38 | Mm_Celera | 8:81013522 | TGTTTTGGCTCCAGC[A/G]TACCATTCTGAACAA | 74841 |
rs32891335 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Usp38 | Mm_Celera | 8:80998984 | AGGCTGCAGTCTTGT[C/T]TCCTATCACATTGTC | 74841 |
rs32892457 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Usp38 | Mm_Celera | 8:81014083 | GAGATCCAGCACCGA[C/T]GGGCAGCTCATAATC | 74841 |
rs32902629 | snp | A/T | 0.32 | 0.24 | intron-variant | Usp38 | Mm_Celera | 8:80990768 | GCTGCTCTTGCACCC[A/T]CAAGACACAAGTATC | 74841 |
rs32908028 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp38 | Mm_Celera | 8:81008964 | TGGGCGAGCAGGGCC[A/G]GAGCAAGCAGAGGCC | 74841 |
rs32916408 | snp | A/G | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Usp38, Gm31223 | GRCm38.p3 | 8:80983990 | TTTCCATCCACCTCC[A/G]TGGGTTCTATTGAAC | 74841 |
rs32921024 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Usp38 | GRCm38.p3 | 8:80985936 | GCCTTTCCTATAACT[A/G]TTCACACTCTTGCAT | 74841 |
rs32923077 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp38 | Mm_Celera | 8:81013344 | GGTTACACACAGTAA[C/T]AATAACTCCCTGCGG | 74841 |
rs32925798 | snp | G/T | 0.48 | 0.0979796 | upstream-variant-2KB | Usp38 | GRCm38.p3 | 8:81015245 | ACGTGGATTCCGTCA[G/T]TGGTGAGGGTTAGAA | 74841 |
rs32962444 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Usp38 | Mm_Celera | 8:81016506 | GCTAAGAAATTAGTG[A/G]TGATTACGAAGAGAC | 74841 |
rs32970222 | snp | A/G | 0.265928 | 0.249492 | intron-variant, nc-transcript-variant | Usp38, Gm31223 | GRCm38.p3 | 8:80984348 | TTGACACATTTTCCA[A/G]GGATACTGAAGCCTA | 74841 |
rs32977812 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp38 | Mm_Celera | 8:80992539 | TTATCCCAAGTGCTG[A/G]GATTACAGATGCGCA | 74841 |
rs32978819 | snp | A/G | 0.387812 | 0.208586 | intron-variant, downstream-variant-500B, nc-transcript-variant | Usp38, Gm31223 | GRCm38.p3 | 8:80980240 | TGTGGGCCTCCGCCA[A/G]TCTTGAGGGTGCTTT | 74841 |
rs32986104 | snp | A/G | 0.375 | 0.216506 | intron-variant, downstream-variant-500B, nc-transcript-variant | Usp38, Gm31223 | GRCm38.p3 | 8:80980632 | TTTTTGCACGCGCGC[A/G]CGTACATATGTGTGT | 74841 |
rs32997558 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Usp38 | Mm_Celera | 8:80988874 | CCTCTGAGTGTATCA[C/T]CAACTCTAAGCCACT | 74841 |
rs33016201 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Usp38 | Mm_Celera | 8:80995648 | CCTTATATCGTATGT[C/T]GCTCACCAAGTCTGG | 74841 |
rs33031378 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Usp38 | Mm_Celera | 8:80993757 | CCATGACTCGATACA[A/G]TGATGGAAAAGGCCC | 74841 |
rs33033011 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp38 | Mm_Celera | 8:81005979 | AAATATTCTAATGAT[C/T]TGGTTTACATTACCG | 74841 |
rs33037050 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp38 | Mm_Celera | 8:81006049 | AAAAGACAAAGGAAT[C/G]TGGGTTCTGATGGAG | 74841 |
rs33076650 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Usp38 | Mm_Celera | 8:80995347 | CAGGAGGGAATTGAG[C/T]ATTGCCTTGCTTCTA | 74841 |
rs33080876 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp38 | Mm_Celera | 8:81003282 | TTATTTAAGTCCATG[C/T]AGCATCTATGGTTAC | 74841 |
rs33085353 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp38 | Mm_Celera | 8:81007238 | GTCCAGAAAAGGATA[C/T]ATAGTAAGACTGTCT | 74841 |
rs33126110 | snp | A/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Usp38, Gm31223 | Mm_Celera | 8:80983352 | TACAAAAATTAACTT[A/T]GCAAAATAATTAGAA | 74841 |
rs33140726 | snp | A/T | 0.5 | 0 | intron-variant | Usp38 | Mm_Celera | 8:81004013 | CTGCCATATCCAGGG[A/T]TCCACCCCATAATCA | 74841 |