SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs946983 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | UBTD1 | GRCh38.p7 | 10:97502837 | TGTGTGTGTGTGCGt[A/G]tgtgtgtatacatat | 80019 |
rs946984 | snp | C/T | 0.363776 | 0.222609 | intron-variant | UBTD1 | GRCh38.p7 | 10:97515599 | GGGATTAGAAAAACC[C/T]TGTTAGATTCTCCCT | 80019 |
rs946985 | snp | G/T | 0.309894 | 0.242719 | intron-variant | UBTD1 | GRCh38.p7 | 10:97515623 | TCTCCCTCTCTCTCA[G/T]CTCTGCTTCTCTTTG | 80019 |
rs946986 | snp | C/G | 0.363776 | 0.222609 | intron-variant | UBTD1 | GRCh38.p7 | 10:97515846 | GCCAAGGGATGGGGT[C/G]ACACGTGATGAAACA | 80019 |
rs946987 | snp | A/G | 0.363359 | 0.222822 | intron-variant | UBTD1 | GRCh38.p7 | 10:97516351 | CTCTTACATGTCGGC[A/G]TGTTCCATGGTTGAA | 80019 |
rs1107517 | snp | C/G | 0.4973 | 0.0366419 | intron-variant | UBTD1 | GRCh38.p7 | 10:97540234 | GTCCTATTCTGTGTA[C/G]AGTCTAGCTGAGTTA | 80019 |
rs1107518 | snp | C/G | 0.475259 | 0.108435 | intron-variant | UBTD1 | GRCh38.p7 | 10:97540103 | ACAGGATCCAGATTT[C/G]TGGAGGAGAGGCGAT | 80019 |
rs1111831 | snp | C/T | 0.089084 | 0.191327 | intron-variant | UBTD1 | GRCh38.p7 | 10:97539573 | GCACTCCAGCCTGGG[C/T]GACAGAGAGAGGCCC | 80019 |
rs1417408 | snp | C/T | 0.498503 | 0.0273153 | intron-variant | UBTD1 | GRCh38.p7 | 10:97538719 | AGAGTCTCTTCCTTC[C/T]GGATCTCAAAGCTTT | 80019 |
rs1417409 | snp | C/G | 0.089084 | 0.191327 | intron-variant | UBTD1 | GRCh38.p7 | 10:97539029 | TGCCTGGCAGTGCTT[C/G]TGTTGCCCTGGGCCT | 80019 |
rs1572860 | snp | C/T | 0.452473 | 0.146644 | intron-variant | UBTD1 | GRCh38.p7 | 10:97551225 | CTCTATACACAGACA[C/T]ATACATTCTCTGCTC | 80019 |
rs1572861 | snp | A/C | | | intron-variant | UBTD1 | GRCh38.p7 | 10:97525043 | CAGAAGATGGAGAGT[A/C]TTTTCACTTGTGTGT | 80019 |
rs1572862 | snp | A/C | | | intron-variant | UBTD1 | GRCh38.p7 | 10:97525063 | CACTTGTGTGTGCTG[A/C]GAGAAGAATATGCCT | 80019 |
rs1890969 | snp | A/G | 0.478768 | 0.100824 | | | GRCh38.p7 | 10:97516329 | TTACAGAGGACCCAG[A/G]CTTCTCCTCTTACAT | 80019 |
rs2153545 | snp | A/T | 0.107341 | 0.205301 | intron-variant | UBTD1 | GRCh38.p7 | 10:97557002 | CAATACTGTCCAATA[A/T]TTGAGACTTTTAGAA | 80019 |
rs2153546 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | UBTD1 | GRCh38.p7 | 10:97557135 | cggttccaacacaaa[C/T]ataacatgaggtgac | 80019 |
rs2153547 | snp | A/C/G | 0.0126979 | 0.078662 | intron-variant | UBTD1 | GRCh38.p7 | 10:97501523 | tgaactggaagtttc[A/C/G]cagaggttgtagtga | 80019 |
rs2185512 | snp | A/G | 0.152001 | 0.229992 | intron-variant | UBTD1 | GRCh38.p7 | 10:97557631 | actatcaatagtggc[A/G]caagcatcaaatttt | 80019 |
rs2211243 | snp | C/T | 0.481703 | 0.0938806 | intron-variant, upstream-variant-2KB | MMS19, UBTD1 | GRCh38.p7 | 10:97496999 | ATTTTCATAATAAAA[C/T]ATGAGGGAAAATGAC | 80019 |
rs2861969 | snp | A/G | 0.152334 | 0.230133 | intron-variant | UBTD1 | GRCh38.p7 | 10:97558513 | TGTTTTGAGAGATAG[A/G]CCACTGCCCTTGGCC | 80019 |
rs3066031 | in-del | -/AG | 0.0854556 | 0.188216 | intron-variant | UBTD1 | GRCh38.p7 | 10:97539939 | GTTTGGAAGGGCCTC[-/AG]GGGCTGCACAGGCAT | 80019 |
rs3750558 | snp | A/C | 0.491501 | 0.0646329 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | MMS19, UBTD1 | GRCh38.p7 | 10:97498466 | CTTGCGCTTCCCCGG[A/C]GATTGGCTCGGGAGG | 80019 |
rs3814552 | snp | A/G | 0.0463947 | 0.145069 | intron-variant, upstream-variant-2KB | MMS19, UBTD1 | GRCh38.p7 | 10:97497258 | TGTTTGGGGAATAAT[A/G]TGTATTCAACAATAG | 80019 |
rs3814554 | snp | C/T | 0.49889 | 0.0235361 | upstream-variant-2KB, downstream-variant-500B | ANKRD2, UBTD1 | GRCh38.p7 | 10:97571444 | GCCATGCTGCCTGCC[C/T]TGCCTCCTCCATCAG | 80019 |
rs4364993 | snp | C/G | 0 | 0 | intron-variant | UBTD1 | GRCh38.p7 | 10:97563182 | acaggtattaaagga[C/G]taagtattgggagaa | 80019 |
rs4595477 | snp | C/T | 0 | 0 | intron-variant | UBTD1 | GRCh38.p7 | 10:97529317 | tcctcacatcccaga[C/T]gatgggcggccaggc | 80019 |
rs4606413 | snp | C/T | 0.21725 | 0.247846 | intron-variant | UBTD1 | GRCh38.p7 | 10:97529078 | gagacgctcctcacc[C/T]cccagacagggtcgc | 80019 |
rs4635019 | snp | C/T | 0.452103 | 0.147154 | intron-variant | UBTD1 | GRCh38.p7 | 10:97551301 | AGCACTTCGGGAGGC[C/T]GAGACAGGAGGATCC | 80019 |
rs4917774 | snp | A/G | 0.491885 | 0.0631791 | intron-variant | UBTD1 | GRCh38.p7 | 10:97522115 | TGAGCTCTGCAAGAC[A/G]TAGACAAGATCACCT | 80019 |
rs4917775 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | UBTD1 | GRCh38.p7 | 10:97553045 | TTCTCAGTACCTCGC[A/G]GAGGCGTGCACCAAT | 80019 |
rs4919102 | snp | C/G | 0.0528381 | 0.153711 | upstream-variant-2KB, intron-variant | MMS19, UBTD1 | GRCh38.p7 | 10:97499928 | CTGGTGATCCTCCAG[C/G]CCCGCGCAACGCTTT | 80019 |
rs4919103 | snp | A/G | 0.373598 | 0.21731 | intron-variant | UBTD1 | GRCh38.p7 | 10:97510249 | GAATTACAGGCATGA[A/G]CCACCTTGCCCAGCC | 80019 |
rs4919104 | snp | G/T | 0.446249 | 0.154875 | intron-variant | UBTD1 | GRCh38.p7 | 10:97520412 | CCCAGTGCCGTGCTT[G/T]ATCCTGGGTGTGCAG | 80019 |
rs4919105 | snp | A/G | 0.491987 | 0.0627894 | intron-variant | UBTD1 | GRCh38.p7 | 10:97520476 | GTCCCACAGAATAAC[A/G]GGGAAACACATGATA | 80019 |
rs4919107 | snp | A/G | | | intron-variant | UBTD1 | GRCh38.p7 | 10:97530223 | atgaatgaatgaatg[A/G]atggatggatgaatc | 80019 |
rs4919108 | snp | A/G | 0.487305 | 0.0786545 | intron-variant | UBTD1 | GRCh38.p7 | 10:97538026 | AGATGGGCTTTCACC[A/G]TGTTGGCCAGGCTGG | 80019 |
rs4919109 | snp | A/T | 0.497558 | 0.0348586 | intron-variant | UBTD1 | GRCh38.p7 | 10:97538197 | TGCTTTGTTTTTAAA[A/T]TTTACATATATTGGC | 80019 |
rs4919110 | snp | A/G | 0.165853 | 0.235413 | intron-variant | UBTD1 | GRCh38.p7 | 10:97546978 | TCTGGGACAAGTCAC[A/G]TCACCTTTCAGCCTT | 80019 |
rs4919111 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | UBTD1 | GRCh38.p7 | 10:97552572 | GGCTAATTTTTGTAT[C/T]TTTGTATTTTTGTAG | 80019 |
rs4919112 | snp | A/C | 0.093417 | 0.194889 | intron-variant | UBTD1 | GRCh38.p7 | 10:97559520 | agaccaaagaaaact[A/C]aacaccattttatat | 80019 |
rs4919113 | snp | A/T | 0 | 0 | intron-variant | UBTD1 | GRCh38.p7 | 10:97566286 | ttttttttttttttt[A/T]aaaaCTATTACCTTA | 80019 |
rs6584131 | snp | A/G | 0.294832 | 0.245947 | intron-variant | UBTD1 | GRCh38.p7 | 10:97513560 | ATTTGAGGAAGTGGT[A/G]CAGGTTGGAGAGAAG | 80019 |
rs6584132 | snp | C/T | 0.294832 | 0.245947 | intron-variant | UBTD1 | GRCh38.p7 | 10:97513826 | CAAGTGATCCTCCCA[C/T]CCCACCTCCTGAGTA | 80019 |
rs6584134 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | UBTD1 | GRCh38.p7 | 10:97553448 | TATCTTTTTAAGTAA[A/G]TGAAATTAATATGTT | 80019 |
rs6584135 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | UBTD1 | GRCh38.p7 | 10:97559296 | ggaccaccttagtgg[A/G]agggggacaatcagg | 80019 |
rs6584136 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | UBTD1 | GRCh38.p7 | 10:97559313 | gggggacaatcaggg[C/T]ctctggcctgccatg | 80019 |
rs7071742 | snp | A/G | 0.273318 | 0.24891 | intron-variant | UBTD1 | GRCh38.p7 | 10:97513137 | GTCTGCTCTGCACAG[A/G]GGTGGTGCTGGTATC | 80019 |
rs7074482 | snp | A/G | 0.355954 | 0.226437 | intron-variant | UBTD1 | GRCh38.p7 | 10:97526246 | atagtctttctggaa[A/G]gcaatttggcaaaag | 80019 |
rs7074782 | snp | A/G | 0.112631 | 0.208878 | intron-variant | UBTD1 | GRCh38.p7 | 10:97526466 | ACTAAAACTCTGCCT[A/G]CCATGATCGACACAA | 80019 |
rs7074898 | snp | A/C | 0.112983 | 0.209108 | intron-variant | UBTD1 | GRCh38.p7 | 10:97526474 | TCTGCCTACCATGAT[A/C]GACACAATAAAATCT | 80019 |
rs7075656 | snp | C/G | 0.48155 | 0.0942576 | intron-variant | UBTD1 | GRCh38.p7 | 10:97520808 | CCCGGTTTCTGCCCT[C/G]TTGGGGTAAGGAGGT | 80019 |
rs7077096 | snp | C/T | 0.211819 | 0.247067 | intron-variant | UBTD1 | GRCh38.p7 | 10:97568905 | CTCGGCTCACCGCAA[C/T]CTGCGCCGCCTGGGT | 80019 |
rs7077130 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | UBTD1 | GRCh38.p7 | 10:97568980 | aggcatgcgccatca[C/T]gcccagctaattttg | 80019 |
rs7077211 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | UBTD1 | GRCh38.p7 | 10:97568880 | ccaggctggaatgca[A/G]tggagcgatctcggc | 80019 |
rs7077652 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | UBTD1 | GRCh38.p7 | 10:97569139 | CAGACCTGGGTTTCA[A/G]TCTGAATGTTTCCCT | 80019 |
rs7077917 | snp | A/G | 0.268995 | 0.249277 | intron-variant | UBTD1 | GRCh38.p7 | 10:97509114 | CTCTCAGCATTTTGC[A/G]GTTttcaaaatgctt | 80019 |
rs7077976 | snp | C/T | 0.498346 | 0.0287064 | intron-variant | UBTD1 | GRCh38.p7 | 10:97553166 | GATGGAGTTTCACTC[C/T]TGTTGCCCAGGCTGG | 80019 |
rs7081548 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | UBTD1 | GRCh38.p7 | 10:97545571 | GGATAATCTTCTTGA[C/T]TATATTTGTGTGTAT | 80019 |
rs7089060 | snp | A/G | 0.498982 | 0.0225409 | intron-variant | UBTD1 | GRCh38.p7 | 10:97522036 | CAACATCAAGTTTCT[A/G]TAGATGGGAGCCCTT | 80019 |
rs7089477 | snp | C/T | 0 | 0 | intron-variant | UBTD1 | GRCh38.p7 | 10:97522203 | GTCCAGCTGCCCACG[C/T]AATGTGGGGTCGTTC | 80019 |
rs7089538 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | UBTD1 | GRCh38.p7 | 10:97559407 | ggcatttgcatcttg[A/G]tgtgctgtcttaatt | 80019 |
rs7089713 | snp | C/T | 0.375598 | 0.21616 | intron-variant | UBTD1 | GRCh38.p7 | 10:97513186 | TCCCTTTCCTGTGCC[C/T]TTTCTAAAATTCCAC | 80019 |
rs7096611 | snp | C/G | 0.458084 | 0.138567 | intron-variant | UBTD1 | GRCh38.p7 | 10:97505693 | CAAGCCTCTTGATCT[C/G]TTTGAGCCTCAGTTT | 80019 |
rs7097951 | snp | A/G | 0.151668 | 0.229849 | intron-variant | UBTD1 | GRCh38.p7 | 10:97553719 | GTGCAGTGATGACTG[A/G]GAAGGCAACGGTTGG | 80019 |
rs7099248 | snp | G/T | 0.375 | 0.216506 | intron-variant | UBTD1 | GRCh38.p7 | 10:97545393 | TATGGGGCTCgtgtg[G/T]gtgtgtgtgtgtgtg | 80019 |
rs7099261 | snp | C/T | 0.5 | 0 | intron-variant | UBTD1 | GRCh38.p7 | 10:97545421 | gtgtgggtgtgggtg[C/T]gtgtgtgtgggtgtg | 80019 |
rs7341998 | snp | A/G | 0.371582 | 0.218444 | intron-variant | UBTD1 | GRCh38.p7 | 10:97524700 | CCTGATGTCCTCAAC[A/G]TGAACAGACCAAGTG | 80019 |
rs7475470 | snp | C/T | 0.451856 | 0.147493 | intron-variant | UBTD1 | GRCh38.p7 | 10:97550746 | GTAAACACACACACA[C/T]GCATACACACTCACA | 80019 |
rs7475592 | snp | A/G | | | intron-variant | UBTD1 | GRCh38.p7 | 10:97551309 | gggaggccgagacag[A/G]aggatcccttgagcc | 80019 |
rs7475851 | snp | C/G | 0.497502 | 0.035255 | intron-variant | UBTD1 | GRCh38.p7 | 10:97562304 | gctactcggtgtcac[C/G]cgcatccatgtgaag | 80019 |
rs7893335 | snp | G/T | 0.429087 | 0.174436 | upstream-variant-2KB, intron-variant | MMS19, UBTD1 | GRCh38.p7 | 10:97500220 | GAACTCAGCCTCCTC[G/T]CCCACCCCATTGCCA | 80019 |
rs7893588 | snp | C/T | 0 | 0 | intron-variant | UBTD1 | GRCh38.p7 | 10:97528066 | GACGGGGCGGCTGGC[C/T]GGGCGGGGGGCTGAC | 80019 |
rs7893594 | snp | C/T | 0 | 0 | intron-variant | UBTD1 | GRCh38.p7 | 10:97528082 | GGGCGGGGGGCTGAC[C/T]CCCCCACCTCCCTCC | 80019 |
rs7895702 | snp | C/G | 0.445196 | 0.1562 | intron-variant | UBTD1 | GRCh38.p7 | 10:97525613 | GCGGCTCACTTCTCC[C/G]TCCACTGGCCTCTGC | 80019 |
rs7897321 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | UBTD1 | GRCh38.p7 | 10:97513634 | TGTAAAAAATGTGAA[C/T]GATATGAGAAAGCTC | 80019 |
rs7902642 | snp | A/G | 0.451732 | 0.147663 | intron-variant | UBTD1 | GRCh38.p7 | 10:97569324 | AACATATTTCTCCAT[A/G]CATTACGTTTTGCCA | 80019 |
rs7906491 | snp | C/T | 0.304396 | 0.258038 | intron-variant | UBTD1 | GRCh38.p7 | 10:97530863 | tttattatataattt[C/T]tattttaaaaatttt | 80019 |
rs7908417 | snp | C/T | 0.290977 | 0.246619 | intron-variant | UBTD1 | GRCh38.p7 | 10:97519063 | AGGGCACTCTCCTAA[C/T]CACTAGAGGAGGAGA | 80019 |
rs7911122 | snp | C/T | 0.499989 | 0.00239614 | intron-variant | UBTD1 | GRCh38.p7 | 10:97533899 | CTGCACTGAAGCCTG[C/T]GTGACAAAGCAAGAC | 80019 |
rs7915501 | snp | G/T | 0.442791 | 0.15916 | intron-variant, upstream-variant-2KB | MMS19, UBTD1 | GRCh38.p7 | 10:97498058 | ATGATTCCCTATAAT[G/T]GGCTACAGGGAGATG | 80019 |
rs7919450 | snp | C/T | 0.084364 | 0.187256 | intron-variant | UBTD1 | GRCh38.p7 | 10:97569678 | CATCATGGTGCTGGC[C/T]GGTTCAGGTTTTGGT | 80019 |
rs7919452 | snp | A/G/T | 0.039522 | 0.134904 | intron-variant | UBTD1 | GRCh38.p7 | 10:97548522 | AGAGTCAggctgggc[A/G/T]cagtggctcacgcct | 80019 |
rs7921253 | snp | C/T | 0.474634 | 0.109726 | intron-variant | UBTD1 | GRCh38.p7 | 10:97530899 | tttttaaatttttta[C/T]ttttttgagacggag | 80019 |
rs7921278 | snp | C/T | 0.40733 | 0.194287 | intron-variant | UBTD1 | GRCh38.p7 | 10:97530948 | gctggagtgcagtgg[C/T]gcgatctcggctcat | 80019 |
rs7921505 | snp | A/G | 0.40733 | 0.194287 | intron-variant | UBTD1 | GRCh38.p7 | 10:97530933 | ggctctgttgcccag[A/G]ctggagtgcagtggc | 80019 |
rs7921653 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | UBTD1 | GRCh38.p7 | 10:97531037 | ggactacaggtgccc[A/G]ccaccacgcccaact | 80019 |
rs7923541 | snp | C/T | 0.499984 | 0.00279548 | intron-variant | UBTD1 | GRCh38.p7 | 10:97519403 | TTGACTTTTCTCTGA[C/T]GATCTTTCCACTTAA | 80019 |
rs10430661 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBTD1 | GRCh38.p7 | 10:97549833 | TCCCTTCAAAAGTTA[C/T]CTAGGCTCTGAGGGT | 80019 |
rs10609684 | in-del | -/GT | 0 | 0 | intron-variant | UBTD1 | GRCh38.p7 | 10:97545432 | GGTGTGTGTGTGTGG[-/GT]GTGTGTGTGTGTGTG | 80019 |
rs10678727 | in-del | -/AT | 0.442898 | 0.188389 | intron-variant | UBTD1 | GRCh38.p7 | 10:97502818 | GATTGTCACTCATAT[-/AT]GTGTGTGTGTGCGTA | 80019 |
rs10732779 | snp | C/T | 0.370568 | 0.219005 | intron-variant | UBTD1 | GRCh38.p7 | 10:97511735 | GAGCATTTCATTTCC[C/T]AAGCCTTCACAGCAG | 80019 |
rs10732780 | snp | A/C | 0.375399 | 0.216275 | intron-variant | UBTD1 | GRCh38.p7 | 10:97511739 | ATTTCATTTCCTAAG[A/C]CTTCACAGCAGCTCC | 80019 |
rs10736118 | snp | C/T | 0.323671 | 0.238899 | intron-variant | UBTD1 | GRCh38.p7 | 10:97511217 | ACACTGATTGTGCAG[C/T]AGGCACTGTAGTAGG | 80019 |
rs10748698 | snp | A/G | 0.432504 | 0.170857 | intron-variant | UBTD1 | GRCh38.p7 | 10:97544220 | ATCTCTTGAACCTGG[A/G]AGGCAGAGGTTGCAG | 80019 |
rs10748699 | snp | C/T | 0.482905 | 0.0908579 | intron-variant | UBTD1 | GRCh38.p7 | 10:97546744 | GCCTTGCTCCTGCCG[C/T]GTGTTTTCCTTGCTG | 80019 |
rs10748700 | snp | C/G | 0.449091 | 0.151204 | intron-variant | UBTD1 | GRCh38.p7 | 10:97553681 | GCCCAGAGGTGCTGC[C/G]GCTGCCCTCTGCTGG | 80019 |
rs10748702 | snp | A/C | 0.0883596 | 0.190715 | intron-variant | UBTD1 | GRCh38.p7 | 10:97561770 | TACTGAGTATAAAAC[A/C]ATATAAAACAATATG | 80019 |
rs10748703 | snp | A/G | 0.089084 | 0.191327 | intron-variant | UBTD1 | GRCh38.p7 | 10:97565305 | GATTCTTTTCTAGGA[A/G]CATCTTTGTTCTTCT | 80019 |
rs10748704 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | UBTD1 | GRCh38.p7 | 10:97568493 | GTGGTGGGATCTCGG[C/T]TCACTGCATCCTTCA | 80019 |
rs10748705 | snp | A/G | 0.0364509 | 0.129988 | upstream-variant-2KB, utr-variant-3-prime | ANKRD2, UBTD1 | GRCh38.p7 | 10:97571056 | AGGCGGGTGGTGGAC[A/G]GCTGGGCTGTCGTGG | 80019 |