SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1030215 | snp | A/G | 0.104504 | 0.2033 | intron-variant | UBA2 | GRCh38.p7 | 19:34468032 | AAGGACTATACCCAA[A/G]TCATACTGGTGACAA | 10054 |
rs1030216 | snp | C/T | 0.339882 | 0.233284 | intron-variant | UBA2 | GRCh38.p7 | 19:34468026 | TATACCCAAGTCATA[C/T]TGGTGACAAGGAAAC | 10054 |
rs1043062 | snp | G/T | 0 | 0 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452029 | AACCCCAGTTAGGCC[G/T]GAAAGACCAGCAGGT | 10054 |
rs1043070 | snp | G/T | 0.375399 | 0.216275 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469503 | TTAATGTAAATACCC[G/T]TAGGTATCATTAATA | 10054 |
rs1477338 | snp | C/T | 0.476314 | 0.106217 | intron-variant | UBA2 | GRCh38.p7 | 19:34453544 | AGAGTGAGACCCTGT[C/T]TCAATTAAAAAAAAA | 10054 |
rs1559196 | snp | A/G | 0.476833 | 0.105105 | intron-variant | UBA2 | GRCh38.p7 | 19:34460314 | GCAAGCAGGAAAGCC[A/G]TGGGGATTCACCTGA | 10054 |
rs1802473 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469864 | ACTATACTTATGGAC[A/C]AAATAAATGGCATCT | 10054 |
rs1802474 | snp | G/T | | | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34438667 | CCGAGTGTTATGAGT[G/T]TCATCCTAAGCCGAC | 10054 |
rs1974818 | snp | A/G | 0.387832 | 0.208572 | intron-variant | UBA2 | GRCh38.p7 | 19:34440198 | tagctgggactacag[A/G]tgcccaccaccacgc | 10054 |
rs2042291 | snp | A/T | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34457179 | tatatatatatatat[A/T]ttttttttttttagt | 10054 |
rs2081062 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | UBA2 | GRCh38.p7 | 19:34434489 | GAAGGCAGAATGTGG[A/C]ATATCAACTTGGAAC | 10054 |
rs2161472 | snp | A/T | 0.0476255 | 0.146781 | intron-variant | UBA2 | GRCh38.p7 | 19:34451967 | TCCTAAAGAAAAAAA[A/T]ATATATATTAGAAAT | 10054 |
rs2287830 | snp | G/T | 0.000823384 | 0.0202735 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428394 | CGGAGGCGGAGGCGG[G/T]AGAACCGAGCCGCGG | 10054 |
rs2863982 | snp | C/T | 0.275999 | 0.248644 | intron-variant | UBA2 | GRCh38.p7 | 19:34436627 | AATAGCAAATGAAGC[C/T]GTGTTGAGGTTTTAA | 10054 |
rs2910411 | snp | C/T | 0.219349 | 0.248114 | intron-variant | UBA2 | GRCh38.p7 | 19:34429035 | AGCGCTGGTCACGAG[C/T]GGGTTTACACACGGA | 10054 |
rs2910412 | snp | A/G | 0.20511 | 0.245937 | intron-variant | UBA2 | GRCh38.p7 | 19:34430256 | GTTTACCTCGACAGC[A/G]CATATAGTTTTAATG | 10054 |
rs2910413 | snp | A/G | 0.204496 | 0.245824 | intron-variant | UBA2 | GRCh38.p7 | 19:34458127 | CCAGCTGCTGATACA[A/G]TGATGGCACCACAGA | 10054 |
rs2965271 | snp | C/G | 0.275732 | 0.248672 | intron-variant | UBA2 | GRCh38.p7 | 19:34457630 | AGAGACACTAAAGCC[C/G]TCCTCTGTAAAATAG | 10054 |
rs2965279 | snp | A/C | 0.39009 | 0.207062 | intron-variant | UBA2 | GRCh38.p7 | 19:34428947 | TACGACAGGGACCTC[A/C]AAATTAAAGTCACAA | 10054 |
rs2965280 | snp | A/G | 0.204803 | 0.245881 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426795 | ATTATCCTCATCTAC[A/G]TAGGCAGAGCATGTC | 10054 |
rs3217243 | in-del | -/TTTATAC | 0.173783 | 0.238112 | intron-variant | UBA2 | GRCh38.p7 | 19:34431960 | ACAAAACCCTTATAC[-/TTTATAC]AACTTTGCAATGTAA | 10054 |
rs3787033 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448435 | CCCCATCTCTAAAAA[C/T]GAAAAAAAAATAGCC | 10054 |
rs3787034 | snp | A/T | 0.476574 | 0.105661 | intron-variant | UBA2 | GRCh38.p7 | 19:34448625 | TGAGCTGGGAGGCAG[A/T]TGTGTGTAGAGGGGT | 10054 |
rs3787035 | snp | A/G | 0.267091 | 0.249415 | intron-variant | UBA2 | GRCh38.p7 | 19:34460118 | GAACTGATTCCATCT[A/G]TGAAACCCCTGCCAT | 10054 |
rs3976812 | in-del | -/CT | 0.427575 | 0.175975 | intron-variant | UBA2 | GRCh38.p7 | 19:34436730 | GTACATTATAATTCT[-/CT]TTCTATAGTTTCAAA | 10054 |
rs4461190 | snp | C/T | 0.166832 | 0.235761 | intron-variant | UBA2 | GRCh38.p7 | 19:34468319 | CATAACCTGTTTTTT[C/T]CCCCCTCACTGAAAT | 10054 |
rs4548999 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34457607 | CCAGTATTCATTGTA[C/T]GGAGAAGCTATTTTA | 10054 |
rs4805080 | snp | C/T | 0.320575 | 0.239832 | intron-variant | UBA2 | GRCh38.p7 | 19:34440999 | gtcttgaccacgtgt[C/T]tattcaggaatacaa | 10054 |
rs6510418 | snp | A/C | 0.306927 | 0.243432 | intron-variant | UBA2 | GRCh38.p7 | 19:34447444 | TTATACTTAAGATGC[A/C]GTAAACTTCGATATG | 10054 |
rs6510419 | snp | C/T | 0.328382 | 0.237395 | intron-variant | UBA2 | GRCh38.p7 | 19:34466460 | CCCAGTTTTATGCTT[C/T]AGCAATAAAAGTTAT | 10054 |
rs7247967 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBA2 | GRCh38.p7 | 19:34449219 | ggattacaggcacgc[A/G]ccacgacgcccagct | 10054 |
rs7251055 | snp | G/T | 0.476487 | 0.105846 | intron-variant | UBA2 | GRCh38.p7 | 19:34455290 | AAGCACCAAGTTTAA[G/T]ATCATTTTTATGGAG | 10054 |
rs7252173 | snp | A/G | 0.476487 | 0.105846 | intron-variant | UBA2 | GRCh38.p7 | 19:34455159 | CTTGGGGCACTGCCA[A/G]TACAGGACCACTTTT | 10054 |
rs7254399 | snp | A/G | 0.391024 | 0.206427 | intron-variant | UBA2 | GRCh38.p7 | 19:34447123 | TGAGTCTCAAAACTG[A/G]AGAATTTGGAGTCTG | 10054 |
rs7258977 | snp | A/G | 0.476314 | 0.106217 | intron-variant | UBA2 | GRCh38.p7 | 19:34468907 | AAATACGTAATGTGT[A/G]AAGTGAAAATGCAGC | 10054 |
rs7259160 | snp | A/G | 0.277796 | 0.24845 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469074 | TCTCATAGTTGATTC[A/G]GATGAAGAAGATTCT | 10054 |
rs8101863 | snp | C/G | 0.476487 | 0.105846 | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426582 | AGACCTGCCCATGTT[C/G]ATCAGCCCAGGTCCC | 10054 |
rs8103093 | snp | C/T | 0.5 | 0 | intron-variant, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34430094 | TCTATTTCTTGTAGC[C/T]ACCAGGGTCTCACTA | 10054 |
rs8105611 | snp | C/T | 0.433673 | 0.1696 | intron-variant | UBA2 | GRCh38.p7 | 19:34446612 | Cttttttttttcttt[C/T]ttttttttttttttt | 10054 |
rs8106423 | snp | C/T | 0.204803 | 0.245881 | intron-variant | UBA2 | GRCh38.p7 | 19:34441913 | gggacagagcgagac[C/T]gtgtctcagaaaaag | 10054 |
rs8107863 | snp | A/G | 0.427879 | 0.175668 | intron-variant | UBA2 | GRCh38.p7 | 19:34440783 | aatacaaaattagcc[A/G]gacatggtggtgggc | 10054 |
rs8108760 | snp | A/G | 0.275464 | 0.2487 | intron-variant | UBA2 | GRCh38.p7 | 19:34455986 | cttgctatgttgtcc[A/G]ggttggtcctgaact | 10054 |
rs8109261 | snp | A/G | 0.167484 | 0.23599 | intron-variant | UBA2 | GRCh38.p7 | 19:34433683 | GTGTGACTGTGGCTC[A/G]GCACAGTGGCTCACG | 10054 |
rs10402704 | snp | C/G | 0.0209421 | 0.100162 | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426370 | TAGTCCAGAGGGCTG[C/G]TGTTGTCTGCACAGC | 10054 |
rs10406064 | snp | A/G | 0.021333 | 0.101051 | intron-variant | UBA2 | GRCh38.p7 | 19:34457915 | TAGTATTAGAGAAAT[A/G]GTAAATAGGTACATA | 10054 |
rs10406714 | snp | A/G | 0.021333 | 0.101051 | intron-variant | UBA2 | GRCh38.p7 | 19:34438984 | gaaactgaggtggtc[A/G]gatcacctgagcgca | 10054 |
rs10412944 | snp | C/G | 0.251859 | 0.249993 | intron-variant | UBA2 | GRCh38.p7 | 19:34463968 | AGCTTTTTAAAAAAT[C/G]AACCTGACTGCTCTA | 10054 |
rs10414774 | snp | A/G | 0.105924 | 0.204309 | intron-variant | UBA2 | GRCh38.p7 | 19:34467936 | GTATGCTTGTTTTAA[A/G]GAGCAATAAATCCAT | 10054 |
rs10426648 | snp | A/G | 0.164873 | 0.23506 | intron-variant | UBA2 | GRCh38.p7 | 19:34466223 | cctatagtcccagct[A/G]cttgggaggctgagg | 10054 |
rs10454110 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456129 | tttttttttttgagg[G/T]ggaatcttgctctca | 10054 |
rs10469318 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431270 | tttttttttttttta[A/G]agatagggtctcact | 10054 |
rs10469319 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431338 | gcttactgcagccta[A/G]aactcctggcctcaa | 10054 |
rs10469320 | snp | A/G | 0.0131862 | 0.0801202 | intron-variant | UBA2 | GRCh38.p7 | 19:34431446 | TCATGGCATTTATCA[A/G]AGTCTGTAGTTGAAC | 10054 |
rs10593398 | in-del | -/TA | 0.305934 | 0.243663 | intron-variant | UBA2 | GRCh38.p7 | 19:34449442 | GTTTGGCTTATTCTC[-/TA]TAAAGATTAAGGATG | 10054 |
rs10645536 | in-del | -/AGTATAA | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34431966 | TGCAAAGTTGTATAA[-/AGTATAA]GGGTTTTGTAAGCCA | 10054 |
rs11084766 | snp | G/T | 0.479421 | 0.0993283 | intron-variant | UBA2 | GRCh38.p7 | 19:34449467 | AAGGATGCTCAGTTA[G/T]TATTGATGGATTAAG | 10054 |
rs11284248 | in-del | -/A | 0.463126 | 0.13068 | intron-variant | UBA2 | GRCh38.p7 | 19:34464558 | GTGAGACTCCAACTT[-/A]AAAAAAAAAAAAAGA | 10054 |
rs11332668 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449088 | TTTTTTTTTTTTTTT[-/T]GAGACTGAGTCTCAC | 10054 |
rs11369547 | in-del | -/A/AA | 0.437683 | 0.165152 | intron-variant | UBA2 | GRCh38.p7 | 19:34465637 | AAAAAAAAAAAAAAA[-/A/AA]TGACAGGAAGGACTG | 10054 |
rs11412446 | in-del | -/G | 0.384785 | 0.210554 | intron-variant | UBA2 | GRCh38.p7 | 19:34449335 | GTCTCCCAAAGTGCT[-/G]GGATTACAGGTGTGA | 10054 |
rs11417384 | in-del | -/T | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34431268 | TTTTTTTTTTTTTTT[-/T]AGAGATAGGGTCTCA | 10054 |
rs11419368 | in-del | -/T | 0.437951 | 0.194726 | intron-variant | UBA2 | GRCh38.p7 | 19:34432560 | TATCTCCGGATTGTG[-/T]TTTTTTTTGTGTGTG | 10054 |
rs11538138 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469704 | CATTAATATACATAG[G/T]GCCATCTAACATTTA | 10054 |
rs11669580 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448355 | atcctagcactttgg[A/G]aggctgaggcgggag | 10054 |
rs11669581 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448369 | gaaggctgaggcggg[A/T]ggatcacttgaggcc | 10054 |
rs11669606 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34448391 | cttgaggccaggagc[A/C/T]caagaccagcctggg | 10054 |
rs11669607 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448393 | tgaggccaggagcac[A/G]agaccagcctgggca | 10054 |
rs11670476 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448360 | agcactttggaaggc[C/T]gaggcgggaggatca | 10054 |
rs11670496 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448377 | aggcgggaggatcac[C/T]tgaggccaggagcac | 10054 |
rs11671472 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | UBA2 | GRCh38.p7 | 19:34448962 | GTTTCCAGCCACATT[A/T]GTTACCCAAGTCATA | 10054 |
rs11673331 | snp | C/T | 0.474453 | 0.110094 | intron-variant | UBA2 | GRCh38.p7 | 19:34461598 | AAACTGGTCAGGAAT[C/T]TCAGTGGCTTCAGCG | 10054 |
rs11673558 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448383 | gaggatcacttgagg[C/T]caggagcacaagacc | 10054 |
rs11878335 | snp | A/G | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34457744 | TTGTAGTCACAAGAT[A/G]AAGGTTTGTGTCTCA | 10054 |
rs11880288 | snp | A/G | 0.137187 | 0.223099 | intron-variant | UBA2 | GRCh38.p7 | 19:34465596 | AGCCGAGATTGCGCC[A/G]TTGCACTCCAGCCTG | 10054 |
rs11882557 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433686 | TGACTGTggctcagc[A/C]cagtggctcacgcct | 10054 |
rs12459392 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442161 | gatcacttgagccta[A/G]gaggtcgaggctgca | 10054 |
rs12608880 | snp | A/G | 0 | 0 | synonymous-codon, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34430656 | TGGAAGATCAAAGGC[A/G]CAGGTAACTATATTT | 10054 |
rs12609299 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443780 | AATATTTGGAATATT[C/T]TAAATTACATGTTTG | 10054 |
rs12609993 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBA2 | GRCh38.p7 | 19:34445336 | TATAACATCTAAATA[A/G]GAGGTAAAATGAGAG | 10054 |
rs12610838 | snp | C/T | 0.327445 | 0.237702 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467632 | ATACAAAAAATTAGC[C/T]GGGCGTGGCAGCATG | 10054 |
rs12975804 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34428586 | GTGAGGGCCGGGCGC[C/G]CGCGCGTGAATGGCG | 10054 |
rs12977307 | snp | C/T | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34456106 | TTTCCttttcttttt[C/T]ttttttttttttttt | 10054 |
rs16969326 | snp | G/T | 0.411074 | 0.191194 | intron-variant | UBA2 | GRCh38.p7 | 19:34449739 | TTCATGTTTCTGTGG[G/T]TTATTTTTGGAGGGG | 10054 |
rs16969328 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | UBA2 | GRCh38.p7 | 19:34459832 | ACTGGTTAGGCAGGA[C/T]GGATTGATTTGAGCT | 10054 |
rs17379565 | snp | A/G | 0.219648 | 0.248151 | intron-variant | UBA2 | GRCh38.p7 | 19:34443993 | GTAGCTTAAGGGAAA[A/G]AAATTGCTATATGTG | 10054 |
rs28377865 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34430011 | CCGCCTCCCAGGCTC[A/C]AGTGATCCTCCACCT | 10054 |
rs28418357 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434541 | CTAGTTATATTAGAA[C/T]AGTGGTGAGTTTAGG | 10054 |
rs28421252 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429992 | TCTCGGCTCACTGCA[A/G]CCTCCGCCTCCCAGG | 10054 |
rs28491202 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429998 | CTCACTGCAACCTCC[A/G]CCTCCCAGGCTCCAG | 10054 |
rs28496236 | snp | C/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427874 | ATGGTTTACATTTTT[C/T]TCTTTTTTGAGACGG | 10054 |
rs28716034 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34443467 | TTTTTTTTGAGACGG[A/T]GTCTTGCTCTGTTGC | 10054 |
rs28730943 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34430014 | CCTCCCAGGCTCCAG[C/T]GATCCTCCACCTCAG | 10054 |
rs34001296 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431906 | CGAAAGCTAATATCG[-/G]TTGCCTACCATGACA | 10054 |
rs34008132 | snp | A/G | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34450852 | TCAAGCGATTCTCCC[A/G]CCTCAGCCTCCCGAG | 10054 |
rs34348531 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429613 | ATTCAATAAACGTTT[-/T]GCCATGTATCATTTA | 10054 |
rs34369046 | in-del | -/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438936 | TAGCTGGCCGGGTGC[-/C]GGTGGCTCACACCTG | 10054 |
rs34432680 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34428625 | TGCGGGGGCTGGGAT[-/T]CGGGGGTTCCGGGGC | 10054 |
rs34502777 | in-del | -/C/T | 5.79509e-05 | 0.00538257 | intron-variant | UBA2 | GRCh38.p7 | 19:34434834 | ACTAATTTTTTTTTT[-/C/T]CCCAAAAACTCATAC | 10054 |
rs34519506 | in-del | -/A | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34439224 | AAAAAAAAAAAAAAA[-/A]TGTGGCCATGACTGT | 10054 |
rs34573455 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34450329 | GAAAAGGAAACCTCC[-/C]AGTTCCGTTGGACTG | 10054 |
rs34582162 | snp | A/G | 0.476052 | 0.106772 | intron-variant | UBA2 | GRCh38.p7 | 19:34451027 | AGGCATAGTCTTGCT[A/G]TGTTGCCCAGATTAG | 10054 |
rs34620023 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | UBA2 | GRCh38.p7 | 19:34455892 | TGATCCGCCCACCTC[G/T]GCCTCCCAAAGTGCT | 10054 |
rs34669674 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444045 | TGTGTTTTTTTTTTG[G/T]TTTTTTTTTTTTTTT | 10054 |
rs35024640 | snp | C/T | 0.410737 | 0.191478 | intron-variant | UBA2 | GRCh38.p7 | 19:34449358 | AGGTGTGAGCCACCA[C/T]GCCTGGCCAGAAATC | 10054 |
rs35028159 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444067 | TTTTTTTTTTTTTTT[-/T]TGTCTCAGAGGTGGA | 10054 |
rs35033516 | in-del | -/A | | | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470093 | ACCCCATCTCTACTA[-/A]AAAAAAAAAAAAAAA | 10054 |
rs35061343 | in-del | -/A | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34438221 | CACTTAGTTTTGCTC[-/A]AAAAAAAAAAAAAAA | 10054 |
rs35084879 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435878 | AATCCCAGCACTTTT[-/T]GGGAACCCGAAGCGA | 10054 |
rs35095058 | in-del | -/TTGA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463597 | TGATTGATTGATTGA[-/TTGA]CTGGAGACAGAGTCC | 10054 |
rs35154880 | in-del | -/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460614 | TGAGGAGACTGCTTG[-/G]AAGAGTGCACATTAG | 10054 |
rs35373946 | in-del | -/A | 0 | 0 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467483 | AAAAAAAAAAAAAAA[-/A]GTCATTTAAGGCCTG | 10054 |
rs35592470 | in-del | -/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431422 | TGCCTGGCCTTTTCC[-/C]TGTCATTCTCATGGC | 10054 |
rs35688347 | in-del | -/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445807 | TGTCCTAAATTGCCC[-/C]TTGAACCCCATAAGC | 10054 |
rs35696396 | in-del | -/T/TT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443459 | TTTTTTTTTTTTTTT[-/T/TT]GAGACGGAGTCTTGC | 10054 |
rs35752060 | in-del | -/TA | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34449443 | TTTGGCTTATTCTCT[-/TA]AAAGATTAAGGATGC | 10054 |
rs35801446 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431509 | TTGCTTGACATGTAC[-/A]GTTGTATAGTTCCTG | 10054 |
rs35829146 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34433149 | TAGCTGGCCAAAAAG[A/G]ATAGGAATTTGAAGG | 10054 |
rs35869290 | in-del | -/A | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426936 | AAATATACATCAAAA[-/A]GCTTTATACAATTTT | 10054 |
rs35915759 | in-del | -/G | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467535 | CCCCAACGCTTTGGG[-/G]AGGCCGAGGCGGGCA | 10054 |
rs45482396 | snp | C/T | 0.0476237 | 0.146782 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466925 | TTGTTGGTGATGCCC[C/T]GGAAAAAGTGGGGCC | 10054 |
rs56854690 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457181 | TAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 10054 |
rs57025615 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462984 | TGCATTTAATCCCAG[C/T]TATTCGGGAGGCTAA | 10054 |
rs57045180 | in-del | -/GTA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34464696 | GGCAAATTCATTGTA[-/GTA]ATTAAACTGGAATAA | 10054 |
rs57170294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34434119 | GAAAAGTCAAAATTA[C/T]GTTTATTTTTTAAGG | 10054 |
rs57324266 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | UBA2 | GRCh38.p7 | 19:34429458 | TTTCCTTTATGTATT[A/C]TATATTTAAGCAAAA | 10054 |
rs57975900 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBA2 | GRCh38.p7 | 19:34461802 | AGCTGGATTGAGCAT[C/T]GTCCAAGGAAAACTA | 10054 |
rs58256335 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431815 | GAAGCAGATTTCAGA[A/T]AGGAACAGAAATATT | 10054 |
rs59179710 | in-del | -/AA | 0.167809 | 0.236103 | intron-variant | UBA2 | GRCh38.p7 | 19:34436101 | TCCAGCCTGGGCAAC[-/AA]GAGCGAAACTCTGTC | 10054 |
rs59475411 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433895 | GCCAGGAGGCAGAGG[C/T]TGCAGTGAGCCTAGA | 10054 |
rs59580124 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450766 | TTTTTTTTTTTTTTT[-/T]GAGACCGTGTCTCGC | 10054 |
rs59854411 | snp | A/C | 0.0360663 | 0.129354 | intron-variant | UBA2 | GRCh38.p7 | 19:34456499 | CTGCCATCTTGATTT[A/C]GTTTTCTATTTAAAC | 10054 |
rs60000238 | snp | G/T | 0.202651 | 0.245475 | intron-variant | UBA2 | GRCh38.p7 | 19:34439612 | AGATGGGAGGATCCC[G/T]TGAGCCCAGGAGTTT | 10054 |
rs60338470 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34433931 | CCACTACACTCCAGC[C/T]TTGGTGACAGAGTGC | 10054 |
rs60349858 | in-del | -/AAAAAAA | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34458586 | AAAAAAAAAAAAAAA[-/AAAAAAA]GAAGGTTGAAAAACC | 10054 |
rs60857340 | snp | G/T | 0.410905 | 0.191336 | intron-variant | UBA2 | GRCh38.p7 | 19:34452375 | AGTGATGTGTTCAGG[G/T]TTTATAATTATGTTG | 10054 |
rs60873964 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440323 | AAAAAAAAAAAAAAA[-/A]TGAAAGGAAAATAGA | 10054 |
rs61166072 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34443555 | CAAGCGATTCTCCTG[C/T]CTCAGCTTCCCGAGT | 10054 |
rs61729883 | snp | A/G | 0.0298439 | 0.118454 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34433377 | TGGAATTTTTCCGAC[A/G]GTTTATACTGGTTAT | 10054 |
rs62123393 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427566 | TTGTTTTTTTGAGAC[A/G]GAGTCTGTTGCCCAG | 10054 |
rs62123395 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450733 | AAATTGCTATATATT[A/T]ATGTATATCTTTTTT | 10054 |
rs62123397 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454441 | CTTTTTTTTTTTTCC[C/T]AGCAATGGCAGGGAA | 10054 |
rs62123398 | snp | C/T | 0.153997 | 0.230832 | intron-variant | UBA2 | GRCh38.p7 | 19:34459369 | AAGGGTATAAGTAAC[C/T]TGCAGAGTTTTGGTT | 10054 |
rs67173600 | in-del | -/AATATATATA | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34457180 | TAAAAAAAAAAAAAA[-/AATATATATA]TATATATATATATAT | 10054 |
rs67809236 | in-del | -/T | 0.488786 | 0.0740357 | intron-variant | UBA2 | GRCh38.p7 | 19:34445456 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 10054 |
rs71165655 | in-del | -/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436733 | GAAACTATAGAAAGA[-/G]AATTATAATGTACTT | 10054 |
rs71165656 | in-del | -/A/AA/AAA | 0.489259 | 0.0724914 | intron-variant | UBA2 | GRCh38.p7 | 19:34441930 | CAAAAAAAAAAAAAA[-/A/AA/AAA]GATAATGTGGCCAGG | 10054 |
rs71351769 | snp | G/T | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34448213 | GTGCCAGAATAATCT[G/T]GAGTACAGCCATCTG | 10054 |
rs71351770 | snp | A/T | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34450739 | CTATATATTTATGTA[A/T]ATCTTTTTTTTTTTT | 10054 |
rs71970755 | in-del | -/T/TT/TTT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443441 | TATCCGTTATTCACT[-/T/TT/TTT]TTTTTTTTTTTTTTT | 10054 |
rs71993254 | in-del | -/AA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436102 | CCAGCCTGGGCAACG[-/AA]AGCGAAACTCTGTCT | 10054 |
rs73030334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34444012 | TTGCTATATGTGCTA[A/G]GTAATGTGTGTTTAA | 10054 |
rs73030348 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34461880 | TGTGAAACGGAGGGG[G/T]AGTAATAGGAGAGGG | 10054 |
rs73584613 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBA2 | GRCh38.p7 | 19:34449776 | CATTTTAAAGATATC[A/G]CAGTTCAGAAGTTCT | 10054 |
rs73584620 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | UBA2 | GRCh38.p7 | 19:34456933 | CCCTTTGAGCTCACC[A/G]ACAGTACTAATTACT | 10054 |
rs74177148 | in-del | -/GA | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34436733 | GAAACTATAGAAAGA[-/GA]ATTATAATGTACTTA | 10054 |
rs74177152 | in-del | -/GATT | 0.353448 | 0.227593 | intron-variant | UBA2 | GRCh38.p7 | 19:34463575 | CTGTCCAGATTTTGG[-/GATT]GATTGATTGATTGAT | 10054 |
rs74497752 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34461042 | GCTAACACATTTGCT[A/G]TACAAGGTACAATAC | 10054 |
rs74551767 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34454788 | CAATTTTACTGAATT[A/C/G]TTCGAAGAATTCATT | 10054 |
rs75080432 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458982 | TATTACTGTGATGAC[A/T]AACAAACACTAGCTG | 10054 |
rs75291661 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | UBA2 | GRCh38.p7 | 19:34451136 | TCTCCTGAGTAGCTG[A/G]GACTGTATGCAACTG | 10054 |
rs75383341 | snp | A/C | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34436118 | AGCGAAACTCTGTCT[A/C]AAAAAAAAAAAAACC | 10054 |
rs75521130 | snp | A/C | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34436119 | GCGAAACTCTGTCTC[A/C]AAAAAAAAAAAACCA | 10054 |
rs75673500 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34431622 | GCTTGCCATTCATGT[A/G]GAAGTGTGTTTGGTG | 10054 |
rs76117509 | snp | C/T | 0.00144196 | 0.0268123 | intron-variant | UBA2 | GRCh38.p7 | 19:34460452 | TAATATTTTGAATCC[C/T]TTTTTTTTTTTTTGT | 10054 |
rs76247461 | snp | A/G | 0.0189856 | 0.0955633 | upstream-variant-2KB, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428299 | AGCACACCCCGGCGC[A/G]ATGTGCCCTGCCTGT | 10054 |
rs76285532 | snp | G/T | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34450761 | TTTTTTTTTTTTTTT[G/T]TTTTTGAGACCGTGT | 10054 |
rs76510368 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34442368 | ATAAGACCATAGTAA[A/G]CTACAGATGCTTCTC | 10054 |
rs76530696 | snp | A/C | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34439206 | AGTGAGAATTTGTCT[A/C]AAAAAAAAAAAAAAA | 10054 |
rs76713624 | snp | A/T | 0.00676609 | 0.0577691 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470325 | TCTTTATTCTTGGAG[A/T]CTTCACATGTAGGAA | 10054 |
rs76940328 | snp | A/C | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34440310 | GAGATGATGTTTCAA[A/C]AAAAAAAAAAAAATG | 10054 |
rs76972034 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458983 | ATTACTGTGATGACA[A/G]ACAAACACTAGCTGC | 10054 |
rs76980352 | snp | G/T | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34460464 | TCCTTTTTTTTTTTT[G/T]TGTAGATAGTGAAAG | 10054 |
rs77015298 | snp | A/G | 0.0311548 | 0.120858 | intron-variant | UBA2 | GRCh38.p7 | 19:34464008 | AACTGAAGTATCTAA[A/G]TTATTCACGTTTCCT | 10054 |
rs77184202 | snp | A/T | 0 | 0 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470111 | AAAAAAAAAAAAAAT[A/T]AGCCGGGCCTGGTGG | 10054 |
rs77247129 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | UBA2 | GRCh38.p7 | 19:34466568 | AATTTGTTGTGTACC[A/G]TCTTTTTTATTATAA | 10054 |
rs77299031 | snp | G/T | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34443459 | TTTTTTTTTTTTTTT[G/T]GAGACGGAGTCTTGC | 10054 |
rs77340642 | snp | A/G/T | 0.0063735 | 0.0560958 | intron-variant | UBA2 | GRCh38.p7 | 19:34460466 | CTTTTTTTTTTTTTT[A/G/T]TAGATAGTGAAAGAA | 10054 |
rs77906346 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34465715 | AGTTAGATAATGGAG[G/T]CAAAGTGGTCCTGCT | 10054 |
rs78044554 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBA2 | GRCh38.p7 | 19:34443330 | CTGATAGGAATGGAT[A/G]TAGGTCTGCTAAAAT | 10054 |
rs78168883 | snp | C/T | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34430485 | TAATGTAGCAGATAT[C/T]AAAAGTTCTGGATTA | 10054 |
rs78361048 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34430969 | CTGCTATGTTTGGGG[A/G]CTAGAGGAGCGTTAT | 10054 |
rs78440777 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | UBA2 | GRCh38.p7 | 19:34432863 | CCCGGCCTGTATCTC[C/T]GGCTTGTTTTTTAGT | 10054 |
rs78449968 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458984 | TTACTGTGATGACAA[A/G]CAAACACTAGCTGCT | 10054 |
rs78767673 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428179 | AGGCGACCCTTAGAC[A/T]TTTTAGGTCTGATGG | 10054 |
rs78770631 | snp | A/C/G | 0.00215281 | 0.0327437 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469093 | GAAGAAGATTCTTCA[A/C/G]ATAATGCCGACGTCA | 10054 |
rs78826918 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444558 | ACGCCCGTAGTCCCA[A/G]CATTTTGGGAGGCTG | 10054 |
rs78868368 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446620 | TTTCTTTCTTTTTTT[C/T]TTTTTTTGAGAGAGA | 10054 |
rs78892828 | snp | G/T | 0.219947 | 0.248187 | intron-variant | UBA2 | GRCh38.p7 | 19:34437780 | TAAAATGGGCTGGGC[G/T]CAGTGGCTCACGCCT | 10054 |
rs78898896 | in-del | -/TT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460464 | TCCTTTTTTTTTTTT[-/TT]GTAGATAGTGAAAGA | 10054 |
rs79131487 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBA2 | GRCh38.p7 | 19:34468130 | TTGAATATTTACTCC[C/T]CTCCCTTTCTTCCTT | 10054 |
rs79133429 | snp | A/C | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34436120 | CGAAACTCTGTCTCA[A/C]AAAAAAAAAAACCAA | 10054 |
rs79492554 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | UBA2 | GRCh38.p7 | 19:34445939 | AATTATTGTTCATCT[A/G]GACCCGTAGGTCCGT | 10054 |
rs79513119 | in-del | -/TTTTTTTTTG | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446619 | TTTTCTTTCTTTTTT[-/TTTTTTTTTG]AGAGAGAATCCTGCT | 10054 |
rs79818228 | snp | A/C | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34439207 | GTGAGAATTTGTCTC[A/C]AAAAAAAAAAAAAAA | 10054 |
rs79943809 | snp | C/G | 0.204189 | 0.245767 | intron-variant | UBA2 | GRCh38.p7 | 19:34436699 | GTAGTTACATTTGAA[C/G]AGTCGTTTTCCATGT | 10054 |
rs79998896 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34468661 | AAATGAGTTGTCATA[C/T]GCACAGTGCTCAGAA | 10054 |
rs80005185 | snp | A/C | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34440928 | AAGACTCCATCTCAA[A/C]AAAAAAAAAAAAAAA | 10054 |
rs80014663 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBA2 | GRCh38.p7 | 19:34456416 | ATTGCGCCCAGCCTC[A/G]ATGCACTCTTAAAAT | 10054 |
rs80105785 | snp | C/T | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34450744 | TATTTATGTATATCT[C/T]TTTTTTTTTTTTTTT | 10054 |
rs80198704 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBA2 | GRCh38.p7 | 19:34458987 | CTGTGATGACAAACA[A/C]ACACTAGCTGCTGAT | 10054 |
rs80314447 | snp | A/T | 0 | 0 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470109 | AAAAAAAAAAAAAAA[A/T]TTAGCCGGGCCTGGT | 10054 |
rs111266442 | snp | C/T | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34463732 | CCTGGCCTCCCAAAG[C/T]GCTGAGATTATAGAT | 10054 |
rs111383493 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBA2 | GRCh38.p7 | 19:34444492 | GTGCTTTGAACTGTT[A/G]TATGTGTAGCTTTCA | 10054 |
rs111533392 | snp | C/T | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34431055 | GTGTTCCTTGGTGAT[C/T]CAGAGTCTTAAAACA | 10054 |
rs111575018 | snp | C/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34434908 | GTGCCTGGCAGCTGA[C/T]GTTCCTCTTATTGAA | 10054 |
rs111593710 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBA2 | GRCh38.p7 | 19:34462144 | CCCTTGACCCCTACC[C/T]TCCAGAGGAAGGGGC | 10054 |
rs111625633 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428291 | CGGGCTGCAGCACAC[A/C]CCGGCGCGATGTGCC | 10054 |
rs111654043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34450622 | AAATGGAATCATACT[A/G]TTGATAAACTCTCAC | 10054 |
rs111701841 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34446559 | CCCAGCTTGTATTTC[A/C/G]TCTTATTTCCTCAGT | 10054 |
rs111714009 | snp | A/G | 0.5 | 0 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466955 | CCAAACAAGCTGAAG[A/G]TGCTGCCAAAAGCAT | 10054 |
rs111823675 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | UBA2 | GRCh38.p7 | 19:34445710 | CCCAAAGTGATGGGA[C/T]TATAGGCGTGAGCCA | 10054 |
rs111992843 | snp | C/T | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34448098 | ATTGAAAGGTGGTCT[C/T]ACAGGATCACTATAA | 10054 |
rs112014906 | snp | C/T | 0.00636936 | 0.0560724 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470296 | ACTGTTTGCCAAAGA[C/T]GAGTACTTTCTTTTC | 10054 |
rs112070726 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34445674 | AACTCCTGACTGCAA[C/G]TGATCTGCCCACCTT | 10054 |
rs112139103 | snp | A/C | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34463242 | CCCTGTCTTTAAAAA[A/C]AATTGATTTGAATGG | 10054 |
rs112351170 | snp | G/T | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34436202 | AAACTTTTTAGGGGT[G/T]TATTTGTGAAGTACT | 10054 |
rs112449545 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBA2 | GRCh38.p7 | 19:34468561 | TCATCCTCTGCTACT[A/G]TGTAAGCTTGGGAAG | 10054 |
rs112654553 | snp | A/G | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34439035 | CCAGCATGGTGAAAC[A/G]CATCTCTACTAAAAA | 10054 |
rs112681972 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | UBA2 | GRCh38.p7 | 19:34456619 | CTAGAGTGCAGTGGC[A/G]CGATCTCAGCTCACT | 10054 |
rs112704483 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34440724 | CTGAGGTCAGGAGTT[C/G]AAGACCAACTTGGCC | 10054 |
rs112929874 | snp | C/T | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34447339 | CTTTTGGCAACACCC[C/T]CACACACACACCCAA | 10054 |
rs112976084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34463613 | TGACTGGAGACAGAG[C/T]CCTAAAAATTTTTTT | 10054 |
rs113052056 | snp | C/T | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34464668 | GTCCAGGTGTTTGAA[C/T]AGTTTAAACAGAGGC | 10054 |
rs113123773 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBA2 | GRCh38.p7 | 19:34458453 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10054 |
rs113133079 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34458351 | ACGAGGTCAGGAGAT[C/G/T]GAGACCATCCTGGCT | 10054 |
rs113140130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34468750 | TTATTAGAATATGTA[C/G]CCTCTGCTTTTCTAT | 10054 |
rs113242502 | snp | C/T | 0.000151272 | 0.00869558 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34451996 | GAGAAGAAACGAATG[C/T]ATCAGATCAACAGAA | 10054 |
rs113288724 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBA2 | GRCh38.p7 | 19:34436342 | TTCGCTCTTGTTGCC[C/T]AGGCTGCAGTGCAGT | 10054 |
rs113337500 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436101 | CTCCAGCCTGGGCAA[A/C]GAGCGAAACTCTGTC | 10054 |
rs113391310 | in-del | -/TTTCTTTTTTTT | 0.256061 | 0.249927 | intron-variant | UBA2 | GRCh38.p7 | 19:34446609 | TGACTTTTTTTTTTC[-/TTTCTTTTTTTT]TTTTTTTGAGAGAGA | 10054 |
rs113567652 | in-del | -/G | 0.5 | 0 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470106 | TAAAAAAAAAAAAAA[-/G]AAATTAGCCGGGCCT | 10054 |
rs113716176 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | UBA2 | GRCh38.p7 | 19:34453884 | TCTGTGTTTGTCCAG[C/T]AACCTTCTCTTTACT | 10054 |
rs113731177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34431594 | GGTTACTTCATGTTG[C/T]ATTTTTGCTGAAGCT | 10054 |
rs113762707 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436102 | TCCAGCCTGGGCAAC[A/G]AGCGAAACTCTGTCT | 10054 |
rs113812938 | in-del | -/G/T | 0.0158469 | 0.0875917 | intron-variant | UBA2 | GRCh38.p7 | 19:34455947 | CCACTGCGCCCGGCC[-/G/T]TTTTTTTTTTAAACT | 10054 |
rs113867910 | in-del | -/AGT | 0.0154538 | 0.0865337 | intron-variant | UBA2 | GRCh38.p7 | 19:34429216 | TGTCATTGCTCTCAC[-/AGT]AGACGGTACACTCGC | 10054 |
rs113892117 | snp | A/C | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34466842 | TCCTTTGCTTTCTAA[A/C]TAGTCATAGCAGTGA | 10054 |
rs113959168 | in-del | -/T | 0.0690472 | 0.172499 | intron-variant | UBA2 | GRCh38.p7 | 19:34454426 | GAAACATACTCATCC[-/T]TTTTTTTTTTTTCCC | 10054 |
rs114174223 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | UBA2 | GRCh38.p7 | 19:34442838 | GCACTCACTAGTTGG[C/G]AAAGCGTTAATTTTA | 10054 |
rs114182112 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UBA2 | GRCh38.p7 | 19:34459477 | GTGGTGGTACACACT[C/T]ATCTAATATGACCTG | 10054 |
rs114208951 | snp | G/T | 0.0322114 | 0.122752 | intron-variant | UBA2 | GRCh38.p7 | 19:34453876 | GCCTGGATTCTGTGT[G/T]TGTCCAGCAACCTTC | 10054 |
rs114265403 | snp | C/G | 0.0134861 | 0.0810011 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34469945 | CTACTGCAGGAATGT[C/G]AAATTCTTTTCATTA | 10054 |
rs114319045 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | UBA2 | GRCh38.p7 | 19:34463558 | GCACATCCCTGATGT[C/G]TCTGTCCAGATTTTG | 10054 |
rs114351382 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | UBA2 | GRCh38.p7 | 19:34456874 | ATACCCAGTTTTTAA[A/G]TTATTTAAAAAAAAT | 10054 |
rs114382700 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | UBA2 | GRCh38.p7 | 19:34465562 | GAATTGTTTGAACCG[A/G]GGAGCCGAGTTTGCA | 10054 |
rs114436691 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34460908 | GGAGATTTTTCTCCA[A/G]GAGTGGGGAAGCCTT | 10054 |
rs114639639 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34433186 | TTTCTTTAAAATCTG[C/T]TTATGTTTGGAAAGA | 10054 |
rs114996835 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | UBA2 | GRCh38.p7 | 19:34447060 | TCACACGATCACAAG[A/G]CCCAACAATAGGCCC | 10054 |
rs115030285 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBA2 | GRCh38.p7 | 19:34462249 | GGGATTTTTACTAAG[A/G]CAGAGGCAGGTGATA | 10054 |
rs115287110 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBA2 | GRCh38.p7 | 19:34463533 | GTCACATAGCCTTTC[C/T]TCTAGGGGTGCACAT | 10054 |
rs115482441 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBA2 | GRCh38.p7 | 19:34457057 | TATCTGGCCGGGCAC[A/G]ATGGCTCACACGTGT | 10054 |
rs115568168 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBA2 | GRCh38.p7 | 19:34431150 | ATATTTTGGCTTCCT[C/T]CTCCAGGAGTACTTT | 10054 |
rs115587317 | snp | G/T | 0.0322114 | 0.122752 | intron-variant | UBA2 | GRCh38.p7 | 19:34449464 | ATTAAGGATGCTCAG[G/T]TAGTATTGATGGATT | 10054 |
rs115698911 | snp | A/G | 0.204496 | 0.245824 | intron-variant | UBA2 | GRCh38.p7 | 19:34453798 | CTACTAAATTGCTTG[A/G]GACTACAGGCATGAG | 10054 |
rs115846432 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBA2 | GRCh38.p7 | 19:34454132 | CTGACTGGTCTTTCC[C/T]TCAGCAACCTCTTGT | 10054 |
rs115879684 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | UBA2 | GRCh38.p7 | 19:34447073 | AGGCCCAACAATAGG[C/T]CCATCTGCAAGCTGA | 10054 |
rs116020636 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | UBA2 | GRCh38.p7 | 19:34447852 | GGCTTTCTAGAGCAG[C/G]TGACATTTAAGCCCA | 10054 |
rs116072554 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBA2 | GRCh38.p7 | 19:34468273 | AGAATTTTGGAGACG[A/G]ACATTCAGATTATGG | 10054 |
rs116187248 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBA2 | GRCh38.p7 | 19:34442907 | AGCTTTGAAATTATA[A/G]TTGGGTGGGGGGTTG | 10054 |
rs116368799 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34452970 | TTCATTGTTATTGTT[A/G]TGCTAGTGATTTGGG | 10054 |
rs116371302 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | UBA2 | GRCh38.p7 | 19:34457423 | ATTTGCAAATGAATT[C/T]CAGCCTGGATTAATG | 10054 |
rs116438851 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34440660 | GGGAATGGGCGCAGT[A/G]TATCATGCCTGTAAT | 10054 |
rs116509266 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34456357 | GGCCTGAAGTGATCC[A/G]CCCTTCTCAGCCTCC | 10054 |
rs116585334 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBA2 | GRCh38.p7 | 19:34452283 | TGGCTTGGATATTTT[C/T]AGCTCTAATTGCTGT | 10054 |
rs116681483 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBA2 | GRCh38.p7 | 19:34455464 | GATGTTGTGTCTGCA[A/G]ACACTTCGCTTTCTT | 10054 |
rs116707155 | snp | A/G | 0.0130921 | 0.0798413 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427294 | GAATCTTTACCTGGA[A/G]TGTGTTGGAGTGCTT | 10054 |
rs116806392 | snp | C/T | 0.00482471 | 0.0488782 | intron-variant | UBA2 | GRCh38.p7 | 19:34434847 | TTTCCCAAAAACTCA[C/T]ACTGTTTGTTTTACT | 10054 |
rs116957878 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | UBA2 | GRCh38.p7 | 19:34432581 | TTTGTGTGTGAGATA[C/G]GGTTTTGCGCTTATT | 10054 |
rs117084290 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBA2 | GRCh38.p7 | 19:34459400 | TCTCTGCGTGTTGGA[C/T]AGTGCCCACTCCCAG | 10054 |
rs117130047 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34443170 | GACTCTGCACCTGAG[A/G]TATATAATAATGTTT | 10054 |
rs117195526 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | UBA2 | GRCh38.p7 | 19:34443174 | CTGCACCTGAGGTAT[A/G]TAATAATGTTTGTTG | 10054 |
rs117221202 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | UBA2 | GRCh38.p7 | 19:34465807 | AAGGACATGTACAAT[A/G]AAGTGGAAATACCAC | 10054 |
rs117268980 | snp | A/C | 0.0629771 | 0.165899 | intron-variant | UBA2 | GRCh38.p7 | 19:34447351 | CCCTCACACACACAC[A/C]CAAGACCAGTACTTT | 10054 |
rs117312212 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34448867 | GAGGGGCTCCTGATA[A/T]TTAGTAATAGTTGAA | 10054 |
rs117346150 | snp | C/T | 0.00170127 | 0.029116 | intron-variant | UBA2 | GRCh38.p7 | 19:34454438 | ATCCTTTTTTTTTTT[C/T]CCCAGCAATGGCAGG | 10054 |
rs117520545 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBA2 | GRCh38.p7 | 19:34454036 | TTGGTGTTCTTGTCA[A/G]ACTCATTACTGGACC | 10054 |
rs117605109 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34457893 | GGTTCTTAATTATTT[G/T]TTTGTTTAGTATTAG | 10054 |
rs117615133 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | UBA2 | GRCh38.p7 | 19:34466066 | GTAGGCCAGGCGTGA[C/T]GGCTCACACCTGTAA | 10054 |
rs117617736 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446606 | TGTTGACTTTTTTTT[G/T]TCTTTCTTTTTTTTT | 10054 |
rs117690571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34446069 | CACCATGTTGCCCAG[A/G]CAGATCTCAAACTCC | 10054 |
rs117721169 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBA2 | GRCh38.p7 | 19:34435088 | AAAATGTAAGGACTT[C/T]TATGCTTATATAAAA | 10054 |
rs117786088 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34459621 | AGTTCCTGTTAAATT[G/T]GCTAGATTTGTGTAT | 10054 |
rs117817768 | snp | C/T | 0.0154538 | 0.0865337 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427830 | GCGTAAGCCACCGCG[C/T]CCGGCAGGTGAAAAT | 10054 |
rs117841319 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | UBA2 | GRCh38.p7 | 19:34437150 | CATTTTTGGTAGAGA[C/T]GAGGTTTTGCCATGT | 10054 |
rs117897631 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | UBA2 | GRCh38.p7 | 19:34436772 | CTGGTTGCGTCTAAT[A/T]TTTTTTGGCAGCTTA | 10054 |
rs117907537 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | UBA2 | GRCh38.p7 | 19:34438933 | AATGTAGCTGGCCGG[G/T]TGCGGTGGCTCACAC | 10054 |
rs117953894 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBA2 | GRCh38.p7 | 19:34445885 | GCCTGTTAAATATTT[C/G]TAGAGAAATCTGTGA | 10054 |
rs118026094 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426939 | ATATACATCAAAAGC[C/T]TTATACAATTTTTAG | 10054 |
rs118033570 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34459558 | GGATTCACCTCTGGA[C/G]CTGAAGCGAGGGAAG | 10054 |
rs118096029 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34463710 | GGGCTTCAGGAATCA[A/G]TCCTTCCCTGGCCTC | 10054 |
rs118115059 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBA2 | GRCh38.p7 | 19:34431095 | TTTGCCTGTCTCCCA[A/G]CCTGTTTGGCAAACC | 10054 |
rs137968380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34446346 | ATAACCGAAAACTCT[C/T]TTTCTTTCTGCTGGA | 10054 |
rs138069169 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBA2 | GRCh38.p7 | 19:34441541 | CAACCCGATAAAGGG[C/T]ATTTTGTAGAAACCT | 10054 |
rs138127413 | snp | A/C | 0.000115389 | 0.0075948 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34443906 | GAGCTGACCCTGAAG[A/C]TGCCTGTGAGTAAAT | 10054 |
rs138339041 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBA2 | GRCh38.p7 | 19:34458190 | CAGGTTGCAGAAGAA[C/T]GCGGAGTCTTATATA | 10054 |
rs138357093 | snp | C/G | 0.00248996 | 0.0351963 | intron-variant | UBA2 | GRCh38.p7 | 19:34468996 | GAGCACAGGTAACTC[C/G]CACGCTTTTACCCAT | 10054 |
rs138412655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466061 | ACATTGTAGGCCAGG[C/T]GTGACGGCTCACACC | 10054 |
rs138543970 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34449795 | TTCAGAAGTTCTGTT[A/C/G]TGAAGCACTTTAGTT | 10054 |
rs138583456 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34469982 | GAACTCGGTCGGGCA[C/T]GGTGGCTCATGCCTG | 10054 |
rs138649503 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBA2 | GRCh38.p7 | 19:34442094 | TTAAAAATTAGCAAG[A/G]CATGGTGGCACATGC | 10054 |
rs138710321 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34465552 | TGAGGCGGGAGAATT[A/G]TTTGAACCGGGGAGC | 10054 |
rs138872924 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449135 | AGTGCAGTGGTGCGA[C/T]CTCAGCTGACTGCAC | 10054 |
rs138962295 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457529 | GAAGCCCAAAATCAA[A/T]CAAATCTTTCTCCCT | 10054 |
rs138988183 | snp | C/T | 0.000828665 | 0.0203383 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445115 | TCCAGTTAAACTTTT[C/T]ACCAAGGTTAGATTT | 10054 |
rs138995048 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBA2 | GRCh38.p7 | 19:34451514 | GAGGTGGTCTTGTAC[A/C]TTTCCTATCTCAGGT | 10054 |
rs139012120 | in-del | -/AAAT | 0.219049 | 0.248077 | intron-variant | UBA2 | GRCh38.p7 | 19:34441466 | TCTCAAAAAAATAAA[-/AAAT]AAATAAATAGATAAA | 10054 |
rs139024537 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34433747 | GGAGGATCACTTGAG[A/G]TCAGGAGTTCGAGAC | 10054 |
rs139070768 | snp | C/T | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467556 | GAGGCGGGCAGATCG[C/T]CTGAGCTCAGGAGTT | 10054 |
rs139281787 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34447994 | TAAGGGGGAGAGTGG[A/G]AAAAGATGACTGGAG | 10054 |
rs139384619 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34443432 | TTATAGTCATTTATC[A/C]GTTATTCACTTTTTT | 10054 |
rs139424607 | snp | A/G | 0.0130921 | 0.0798413 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470343 | TCACATGTAGGAAGA[A/G]TACTTTCTAAAATAA | 10054 |
rs139440257 | snp | A/G | 1.78599e-05 | 0.00298824 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34454470 | AACATTATTCCTGCT[A/G]TTGCTACTACTAATG | 10054 |
rs139651096 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UBA2 | GRCh38.p7 | 19:34461163 | ACTTTTGCAGCTCAT[A/T]TCTTGAGTTGCTGTT | 10054 |
rs139709624 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBA2 | GRCh38.p7 | 19:34454917 | TCAGTCATTCTCCTA[C/T]TGAGTCATTCTTTTC | 10054 |
rs139777601 | in-del | -/AAC | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454645 | AATTTTTAAAATGAA[-/AAC]AATAAAATTGGTTTA | 10054 |
rs139790225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453762 | CAAACTCCTGAGCTC[A/C]GGCAATCTGCTTGCC | 10054 |
rs139981483 | in-del | -/TGAT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463586 | TTGGGATTGATTGAT[-/TGAT]TGATTGATTGACTGG | 10054 |
rs139984797 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426725 | TTTTTAACATGATCA[A/T]CCCCTTCCCTTCAGC | 10054 |
rs140017325 | snp | G/T | 0.00168167 | 0.0289483 | intron-variant | UBA2 | GRCh38.p7 | 19:34443824 | GTTATACAGAAGTAT[G/T]TACTATTCTTAAATT | 10054 |
rs140193441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34447707 | TTTGAACAATAAATT[C/T]CAGCTTCAGAGTCTT | 10054 |
rs140260202 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34462756 | AGATCACTTGAGGCC[A/G]GGAGTTTGAGACCAG | 10054 |
rs140330177 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBA2 | GRCh38.p7 | 19:34441181 | ACTTACTAGGCCGGG[C/T]GAGGTGGCTCACGCC | 10054 |
rs140435786 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34435896 | GAACCCGAAGCGAGC[A/G]GATCACCTGAGGTCA | 10054 |
rs140463684 | snp | C/T | 0.000214842 | 0.0103622 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34433372 | TAATGTGGAATTTTT[C/T]CGACAGTTTATACTG | 10054 |
rs140619455 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | UBA2 | GRCh38.p7 | 19:34444652 | TCTCTACAAAAAATA[C/T]AAAAATTAGCCAGGC | 10054 |
rs140648798 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463500 | TCCTTTGCTTGCAGA[A/T]AGCTGCCTTTCTGTT | 10054 |
rs140746726 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBA2 | GRCh38.p7 | 19:34449501 | ATTTTGATAGAAATG[G/T]CTGTGATTTTTAAAT | 10054 |
rs140851518 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBA2 | GRCh38.p7 | 19:34445216 | AATAGTCCATAAAAT[C/T]GAATTAAGCTTCTAT | 10054 |
rs140912426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467688 | GGCTGAGGCAGGAGG[C/T]GGAGGTTGCAGTGAG | 10054 |
rs141092443 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34445792 | CAGTTTGACTGACAT[G/T]TGTCCTAAATTGCCC | 10054 |
rs141098941 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBA2 | GRCh38.p7 | 19:34464785 | ATCATTTCGTTTGTG[A/G]TTTTGTGGCAATAAC | 10054 |
rs141268205 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UBA2 | GRCh38.p7 | 19:34440782 | AAATACAAAATTAGC[C/T]GGACATGGTGGTGGG | 10054 |
rs141304557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34437136 | CTGGCTAATTTTTGC[A/G]TTTTTGGTAGAGATG | 10054 |
rs141373058 | in-del | -/C | 0.226779 | 0.248919 | intron-variant | UBA2 | GRCh38.p7 | 19:34463820 | AGCCCACCCTACTTG[-/C]CCCATTTAAATTTAA | 10054 |
rs141446035 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | UBA2 | GRCh38.p7 | 19:34449011 | CTTTGTACCCATTTC[A/C]CATGTTGCTGTCATA | 10054 |
rs141497196 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427156 | AGGCTGGAGTGCAGT[A/G]GTAAGGGCATAGCTC | 10054 |
rs141509810 | in-del | -/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449065 | AGATAAAATATAAAT[-/C]TTTTTTTTTTTTTTT | 10054 |
rs141614692 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | UBA2 | GRCh38.p7 | 19:34438160 | TTAATCTTGTAGTTT[A/T]CTTAATTTCAGGAGA | 10054 |
rs141680753 | in-del | -/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460675 | TTGCAGAGAGTGGCA[-/G]GTGTTTGGTCATGAA | 10054 |
rs141791919 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34437676 | AAGATGATTCATTTG[A/G]TAGTTTTGAAAAGTT | 10054 |
rs141852144 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34433197 | TCTGCTTATGTTTGG[A/G]AAGAGTCAAACCTTA | 10054 |
rs141853949 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | UBA2 | GRCh38.p7 | 19:34453231 | TTCACAGCCAGCCAA[G/T]AAATACATAAAGAAC | 10054 |
rs141922612 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34447724 | AGCTTCAGAGTCTTA[A/T]TGACATTAAGTTCAG | 10054 |
rs141965926 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34447104 | GGAGCAAGGAGAGCC[A/T]GTCTGAGTCTCAAAA | 10054 |
rs142134488 | snp | A/G | 0.0020753 | 0.0321457 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34450285 | TAAAGATGACATCAG[A/G]TATCTGTTGACAATG | 10054 |
rs142218795 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBA2 | GRCh38.p7 | 19:34466801 | CATAGTGTATGCTTT[C/G]AGGAACAACAGGATT | 10054 |
rs142249000 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34451648 | CGCCTCCCGGGTTCG[C/T]GCCATTCTCCTGCCT | 10054 |
rs142533716 | snp | C/G | 0.0887219 | 0.191022 | intron-variant | UBA2 | GRCh38.p7 | 19:34432782 | CTGGTCTCAAACTCC[C/G]GACCTCAGGTGATCC | 10054 |
rs142550496 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452028 | GAACCCCAGTTAGGC[C/T]TGAAAGACCAGCAGG | 10054 |
rs142594825 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34444684 | TGGTGGTGCATACCT[C/G]TAGTCCCAACTACTT | 10054 |
rs142599494 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426411 | GGCATTCTAGGGGGG[A/G]GGAGAGCAGCGAAAG | 10054 |
rs142648892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34429883 | AATTTAATATTTTGT[A/G]CTTGAAAGAGTAATT | 10054 |
rs142658514 | in-del | -/AAACTAG | 0.0626037 | 0.165477 | intron-variant | UBA2 | GRCh38.p7 | 19:34461812 | AGCATCGTCCAAGGA[-/AAACTAG]AAAGAGTGTGTACAC | 10054 |
rs142716574 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBA2 | GRCh38.p7 | 19:34442096 | AAAAATTAGCAAGGC[A/G]TGGTGGCACATGCCT | 10054 |
rs142750074 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34439248 | TGACTGTTCAGGAAA[C/G]TTAGTCTTATATTGG | 10054 |
rs142751343 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBA2 | GRCh38.p7 | 19:34440116 | GTCACTTGAGGCCAG[A/G]AGTTTGAGAACAGCC | 10054 |
rs143040128 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBA2 | GRCh38.p7 | 19:34455621 | AATGGTACTGTTATT[G/T]TGCAGTGTCATTGAT | 10054 |
rs143070624 | snp | A/T | 1.65078e-05 | 0.00287291 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445007 | TTTTATAGGGGAACC[A/T]ACGGAAGCCGAAGCC | 10054 |
rs143105006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34460946 | TGTTCCTACTATATA[A/G]CAGAAAGATTATTGA | 10054 |
rs143105576 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34447069 | CACAAGGCCCAACAA[C/T]AGGCCCATCTGCAAG | 10054 |
rs143209961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34441972 | AGGTGCAGTGACACA[C/T]ACCTGTAATCCCGGC | 10054 |
rs143291816 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431967 | TGCAAAGTTGTATAA[A/G]GGTTTTGTAAGCCAA | 10054 |
rs143595423 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | UBA2 | GRCh38.p7 | 19:34437811 | GTAATCCCAGCACTT[C/T]TGGGAAGCCAAGGCG | 10054 |
rs143621344 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | UBA2 | GRCh38.p7 | 19:34444283 | GGCTGGTCTCGAACT[C/G]TTGACCTGAGGTGAT | 10054 |
rs143687364 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBA2 | GRCh38.p7 | 19:34441004 | GACCACGTGTCTATT[C/T]AGGAATACAAGCATG | 10054 |
rs143701767 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34431659 | GGGTCAGGGGGGGCT[A/C/T]TCCGGTTATTTTATA | 10054 |
rs143772310 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34464263 | GTATATTTGGTTGAG[C/T]TGGTCACTGAGTTCC | 10054 |
rs143940428 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34433853 | GTCCCAGCTTCTCCG[A/G]AGGCTGAGGTGGGAG | 10054 |
rs144033662 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34463004 | CGGGAGGCTAAGGCA[A/G]GAGAATCGCCTGAAC | 10054 |
rs144238040 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBA2 | GRCh38.p7 | 19:34459499 | TATGACCTGATTCTG[A/G]TATGGTAAGTTAGTC | 10054 |
rs144433442 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBA2 | GRCh38.p7 | 19:34448621 | TAAGTGAGCTGGGAG[G/T]CAGATGTGTGTAGAG | 10054 |
rs144502696 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431970 | AAAGTTGTATAAGGG[A/T]TTTGTAAGCCAAATA | 10054 |
rs144517203 | snp | A/G | 6.58903e-05 | 0.00573941 | missense, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458842 | ATCCTCCCAACCCCA[A/G]TTGTTATGTATGTGC | 10054 |
rs144724689 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | UBA2 | GRCh38.p7 | 19:34437257 | ATGAGCCACCACGCC[C/T]GGCCAGACATTGCTT | 10054 |
rs144796148 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBA2 | GRCh38.p7 | 19:34432974 | CCTAGGGGCCTGAAC[C/T]CTGCCTGATCCTGAT | 10054 |
rs144823950 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439746 | GATCAGTTGAGCCTG[A/G]GAGGTTGAGGCTGCA | 10054 |
rs144918245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435213 | GACCAGCCTGGCAAG[C/T]ATGGTGAAACCCCAT | 10054 |
rs145118096 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34450633 | TACTATTGATAAACT[C/G]TCACTTGCTTTTGTC | 10054 |
rs145130760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34455147 | TATATTTGGGTGCTT[C/G]GGGCACTGCCAATAC | 10054 |
rs145219113 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469057 | CAAGAGCAAGATGAC[A/G]TTCTCATAGTTGATT | 10054 |
rs145230611 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBA2 | GRCh38.p7 | 19:34436471 | CGCCTGGCTAATTTT[A/G]TATTTTTAGTAGAGA | 10054 |
rs145261938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34461617 | GTGGCTTCAGCGTGA[C/G]CCTTCTGTACGGAAT | 10054 |
rs145263795 | in-del | -/TGAC | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463598 | GATTGATTGATTGAT[-/TGAC]TGGAGACAGAGTCCT | 10054 |
rs145277316 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34448293 | TATGGTGAAGATCAG[C/T]GGAATAAAAAATGGT | 10054 |
rs145293654 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34454943 | TTTTCAATTTTATTG[G/T]ATAGTTTTTGATAAT | 10054 |
rs145343604 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UBA2 | GRCh38.p7 | 19:34468071 | ATTTTCAGTGCTGGT[C/G]CTTGGTATTTTTCCA | 10054 |
rs145463416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34462654 | AAAAAAGTGGGGGGA[A/G]ACTGAAAATTGAGAT | 10054 |
rs145518003 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBA2 | GRCh38.p7 | 19:34434378 | ACCTCAGCCTCCCAG[A/G]ATGCTGAGATTATGG | 10054 |
rs145540154 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34448167 | TATTCATATTATAAC[C/T]AATCTGGGACAGTGC | 10054 |
rs145584175 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBA2 | GRCh38.p7 | 19:34429508 | ATGATACTTTTTTAA[C/T]CATGTGTAAAAGTTT | 10054 |
rs145708498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34430414 | TTACATGCATTAAAT[C/T]ATTCTTTATCAGTTT | 10054 |
rs145878229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34457799 | GTTTCTGTTGGATCT[C/T]GCTAGTGTTTTCTAA | 10054 |
rs145937374 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431969 | CAAAGTTGTATAAGG[G/T]TTTTGTAAGCCAAAT | 10054 |
rs146024864 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426598 | ATCAGCCCAGGTCCC[C/T]GCCCTCACCCACTCC | 10054 |
rs146138948 | snp | A/C/T | 1.64906e-05 | 0.00287142 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445091 | ATGGGCTAAATCAAC[A/C/T]GGATATGATCCAGTT | 10054 |
rs146147132 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | UBA2 | GRCh38.p7 | 19:34447299 | GGGTTTGCTTTTCCC[A/G]GTCCACTGACTCAAA | 10054 |
rs146166130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443717 | AATGTTGGGATTAAA[A/G]GTGTGAGCCACTGCG | 10054 |
rs146253134 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432877 | CGGCTTGTTTTTTAG[-/T]TTTTTTACTCTGTGA | 10054 |
rs146273502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430252 | TAGTGTTTACCTCGA[C/T]AGCACATATAGTTTT | 10054 |
rs146304790 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | UBA2 | GRCh38.p7 | 19:34447932 | CTCTGAATAGGGTAC[A/C]GTATGTACAAGGAAA | 10054 |
rs146405147 | snp | A/G | 0.00168845 | 0.0290065 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34451991 | TTTAGGAGAAGAAAC[A/G]AATGCATCAGATCAA | 10054 |
rs146443394 | snp | C/T | 0.0252325 | 0.109451 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467648 | GGGCGTGGCAGCATG[C/T]GTCTGTAGTCCCAGC | 10054 |
rs146462714 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBA2 | GRCh38.p7 | 19:34463496 | TCTCTCCTTTGCTTG[C/T]AGATAGCTGCCTTTC | 10054 |
rs146650320 | snp | G/T | 0.000247188 | 0.0111145 | missense, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34430578 | TATGCATTTGTAGAT[G/T]GATCTGGATACTATT | 10054 |
rs146827638 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34441047 | AAATCTGTAAATGTC[A/G]TTCACTCATTAGGAA | 10054 |
rs146934526 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | UBA2 | GRCh38.p7 | 19:34446209 | ACAGAGCTTAAAACT[G/T]TCTCAGCTCTTATCA | 10054 |
rs147040828 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBA2 | GRCh38.p7 | 19:34468491 | TTTGATTTTGTTGGA[C/T]GAGGAGATAAAACCA | 10054 |
rs147316480 | in-del | -/GGT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438192 | ATAAGGATATGGCTG[-/GGT]TATTCCCCAGACCCA | 10054 |
rs147372433 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | UBA2 | GRCh38.p7 | 19:34442319 | CAATAAGCAAGTTAT[G/T]TTTTAATCATAAGAC | 10054 |
rs147388932 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34439345 | ACCCATTGGTTATAA[A/C]AGAAATCACAATGGA | 10054 |
rs147493298 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBA2 | GRCh38.p7 | 19:34461153 | CTCCTTGGTCACTTT[C/T]GCAGCTCATTTCTTG | 10054 |
rs147560800 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | UBA2 | GRCh38.p7 | 19:34449226 | AGGCACGCGCCACGA[C/G]GCCCAGCTGATTTTT | 10054 |
rs147720348 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | UBA2 | GRCh38.p7 | 19:34434429 | CGTGAAATTACTCTC[G/T]TAACCTGACTCATCT | 10054 |
rs147737948 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429780 | GGTCGAGGCTGCAGT[A/G]AGCTGTGTTTGCACC | 10054 |
rs147840845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34448665 | GTAGGAGAAGGTGAT[A/G]ATAATCAATTTTGAA | 10054 |
rs147843395 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450426 | CGCGTAAAGTCTTTG[-/T]TATAGCCCTGTTGTT | 10054 |
rs147848976 | snp | C/T | 5.92212e-05 | 0.00544124 | synonymous-codon, intron-variant | UBA2 | GRCh38.p7 | 19:34460547 | AATCCTAATATCTTC[C/T]GAAGAGGGAGAGACG | 10054 |
rs147965114 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34468272 | GAGAATTTTGGAGAC[A/G]AACATTCAGATTATG | 10054 |
rs148068116 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34438045 | GACAGAGCAAGACTC[C/T]GTCTCCCCACCGCCA | 10054 |
rs148121653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34432590 | GAGATAGGGTTTTGC[A/G]CTTATTGCCCAGGCT | 10054 |
rs148138329 | snp | C/G | 0.0581099 | 0.160244 | intron-variant | UBA2 | GRCh38.p7 | 19:34447099 | GCTGAGGAGCAAGGA[C/G]AGCCAGTCTGAGTCT | 10054 |
rs148148270 | in-del | -/TTTATTTG | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436298 | GTTTTGGTTTATTTA[-/TTTATTTG]TTTATTTTTTTGAGA | 10054 |
rs148155522 | snp | G/T | 0.0299083 | 0.118682 | intron-variant | UBA2 | GRCh38.p7 | 19:34464415 | ATGCAAAAATTAGCC[G/T]GGCATAGTGGCAGGC | 10054 |
rs148312276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34460359 | AAGAGTGACTTCGCC[A/G]GTTTCCAATAAATAG | 10054 |
rs148322312 | snp | A/G | 0.00378176 | 0.0433195 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431896 | GCAGTTTTACCCGAA[A/G]GCTAATATCGTTGCC | 10054 |
rs148416243 | snp | C/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427827 | CAGGCGTAAGCCACC[C/G]CGCCCGGCAGGTGAA | 10054 |
rs148423918 | snp | G/T | 0.00278517 | 0.0372132 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452021 | ACAGAATGAACCCCA[G/T]TTAGGCCTGAAAGAC | 10054 |
rs148429939 | in-del | -/CCC | | | upstream-variant-2KB, cds-indel, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428221 | GGTGTGGGAATAACA[-/CCC]CCGCCGGTCTCAGCT | 10054 |
rs148503756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34452564 | TTCAGAGGTCTGAAA[A/G]ACAGAGCTCTTGATA | 10054 |
rs148589197 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBA2 | GRCh38.p7 | 19:34439772 | CTGCAGTGAACCGAG[A/G]TAGTGCCACTGCACT | 10054 |
rs148643643 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34434141 | TTTTTAAGGCTTGGG[A/G]GGTCTCACTGTTGCC | 10054 |
rs148658442 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34448472 | GGTGGCCTGAGCCTG[C/T]GGTCCCCAGCTACTC | 10054 |
rs148678686 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | UBA2 | GRCh38.p7 | 19:34466704 | TTCAAGACCAGCCTG[G/T]GCAACATTATGAGAC | 10054 |
rs148939912 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34431471 | TTGAACTTAATCTGG[A/G]TTGTTATTTGATTAA | 10054 |
rs149027961 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34455222 | CCACAAACCTGCACG[C/T]GCCCTATGTTATTGT | 10054 |
rs149114359 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBA2 | GRCh38.p7 | 19:34441543 | ACCCGATAAAGGGTA[G/T]TTTGTAGAAACCTTC | 10054 |
rs149201699 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34468076 | CAGTGCTGGTGCTTG[G/T]TATTTTTCCAAATAA | 10054 |
rs149301978 | in-del | -/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446612 | CTTTTTTTTTTCTTT[-/C]TTTTTTTTTTTTTTT | 10054 |
rs149306899 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34469997 | CGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 10054 |
rs149442301 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446607 | GTTGACTTTTTTTTT[A/T]CTTTCTTTTTTTTTT | 10054 |
rs149466418 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBA2 | GRCh38.p7 | 19:34433796 | GAAACCGTCTCTACC[A/G]AAAAACACAAAAATT | 10054 |
rs149553268 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBA2 | GRCh38.p7 | 19:34458281 | AAGGTTGAGGCCGGG[C/T]GCGGTGGCTCACGCC | 10054 |
rs149607843 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34450544 | GCCACTAATAACATT[C/T]TCAGGAGTGTTCTGG | 10054 |
rs149656152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34461930 | TTGAAGTAGTAGTGA[A/G]GACTCCCTGGACAAA | 10054 |
rs149772907 | in-del | -/AAGTAT | 0.0505692 | 0.150756 | intron-variant | UBA2 | GRCh38.p7 | 19:34434040 | TACTTCCACATGTAA[-/AAGTAT]ATCTACTAAGTGAGT | 10054 |
rs149997450 | in-del | -/GTCAAG | 0.00993419 | 0.0697739 | intron-variant | UBA2 | GRCh38.p7 | 19:34461358 | AAATTCAGGTTTAGT[-/GTCAAG]GTCAAGGTTCTTCTT | 10054 |
rs150007175 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34448288 | ATGTATATGGTGAAG[A/C]TCAGTGGAATAAAAA | 10054 |
rs150022993 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBA2 | GRCh38.p7 | 19:34468019 | TGTTAGAGTTTCCTT[A/G]TCACCAGTATGACTT | 10054 |
rs150061644 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34443567 | CTGCCTCAGCTTCCC[A/G]AGTAGCTGGGATTAC | 10054 |
rs150110816 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34449566 | ATAAATGTGTTGAAT[A/G]AATTAATCAACAATA | 10054 |
rs150162623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34445627 | ATTTTTAGTAGAAGC[A/G]GGGTCTCACCATGTT | 10054 |
rs150231883 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469853 | CTCAAATAACGACTA[C/T]ACTTATGGACCAAAT | 10054 |
rs150282508 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34465519 | GCATGTGCCTGCAGT[C/G]CCAGCTACTCAGGAG | 10054 |
rs150358207 | in-del | -/GG | 0.021333 | 0.101051 | intron-variant | UBA2 | GRCh38.p7 | 19:34429126 | TAACAGATGAGGAAA[-/GG]GGGAGACGCAATGGG | 10054 |
rs150396555 | snp | C/T | 0.00113632 | 0.023809 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34438743 | ACCTATACATTGCAT[C/T]GTTTGGGCAAAGTAC | 10054 |
rs150514452 | snp | A/G | 0.000181472 | 0.00952381 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452132 | GGGGGATGGAGCTGA[A/G]CTCATATGGGATAAG | 10054 |
rs150581978 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | UBA2 | GRCh38.p7 | 19:34461635 | TTCTGTACGGAATAC[A/C]TGTGGTATGGAGGGT | 10054 |
rs150633364 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34453443 | TATGTGAGAGAGTGG[A/T]GCATATGAAGAGAGT | 10054 |
rs150809044 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467341 | ACCACGCATGGTAGC[G/T]TGTACCTGTAGTCTC | 10054 |
rs150809947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34433219 | CAAACCTTACTATCT[A/G]TATGACATATAATCC | 10054 |
rs150879791 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442952 | GTAAGATAACTTTCA[G/T]TAATCATATACTTGA | 10054 |
rs150967930 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34429427 | AAGTACGGGTGGCCG[A/C]CTGAGTCATTGTTTC | 10054 |
rs150982980 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34445189 | GTATTGTTCTAGTTC[A/T]GCTTGTTTTAAAATA | 10054 |
rs151160747 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | UBA2 | GRCh38.p7 | 19:34455731 | TCACTGCAACCTCCA[C/T]CTCCCAGGATCAAGC | 10054 |
rs151335384 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UBA2 | GRCh38.p7 | 19:34435563 | GGCTGCGTGCAGTGG[C/T]TCATGCCTGTAATCC | 10054 |
rs180680062 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431642 | TGTGTTTGGTGGTAC[A/G]TGGGTCAGGGGGGGC | 10054 |
rs180698739 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34451804 | GTCTGCCTCGGCCTC[C/G]CAAAGTGCTGGGATT | 10054 |
rs180736404 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442318 | GCAATAAGCAAGTTA[C/T]GTTTTAATCATAAGA | 10054 |
rs180745568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34464639 | TCAGTGGTGGCTTAT[C/T]AGAAAGACCTAGAGT | 10054 |
rs181247982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447134 | ACTGGAGAATTTGGA[A/G]TCTGATGTTTGAGGG | 10054 |
rs181277881 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBA2 | GRCh38.p7 | 19:34437407 | CTGAGGTAAGGAGTT[C/T]GAGACCAGCCTGGCC | 10054 |
rs181356652 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453636 | TCAAGTGATCCCGCC[A/C]CCTCAGGCTCCCGAG | 10054 |
rs181386926 | snp | A/G | 0.000148318 | 0.00861028 | intron-variant | UBA2 | GRCh38.p7 | 19:34431834 | AACAGAAATATTGTA[A/G]TAATTCAGTGTTGTT | 10054 |
rs181488615 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438366 | AAGGTAAACTCATAT[A/T]TGACACTCAGGTGTA | 10054 |
rs181519550 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34448411 | ACCAGCCTGGGCAAT[A/T]TAGCAAGACCCCATC | 10054 |
rs181695089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34457647 | GCTTTAGTGTCTCTT[C/G]AGGGATTTAGTTCTG | 10054 |
rs181747045 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34454178 | ATAGTATTATAAACA[C/T]GTGAAAGTATTGTTC | 10054 |
rs181844738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34441273 | ATCCTGGCTAACACG[A/G]TGAAACCCCATCTCT | 10054 |
rs181849508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34464278 | TTGGTCACTGAGTTC[C/T]GTGATGTTTGACCTA | 10054 |
rs181964698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34438958 | TCACACCTGTAATCC[C/T]GGCACTTTGGGAAAC | 10054 |
rs181973036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34458018 | ATGTTGATTCTAGAC[A/T]ACTGTGAAAGGCACT | 10054 |
rs181996551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34468557 | GGCTTCATCCTCTGC[C/T]ACTATGTAAGCTTGG | 10054 |
rs182081954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34433757 | TTGAGGTCAGGAGTT[C/T]GAGACCAACCTAGTC | 10054 |
rs182228830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34439075 | TAGTTGGCCGTGATG[C/G]CGAGTGCCTGTAATC | 10054 |
rs182236980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34466475 | CAGCAATAAAAGTTA[C/T]TTACTGTTTTAAAGA | 10054 |
rs182237926 | snp | C/T | 0.00555304 | 0.0523993 | intron-variant | UBA2 | GRCh38.p7 | 19:34458733 | TATAAAATTACAGCA[C/T]GTTTCCGATTTCTGC | 10054 |
rs182241369 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34428805 | GCCGAGGAGGCCGCG[C/G]GCCCCCGCCTCCCCG | 10054 |
rs182372775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34433592 | ATGACTTATTCCAGG[C/T]GGGAATTTAGCTATC | 10054 |
rs182531760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34446896 | CAGGCATGAGCCGTC[A/G]TGCCCAGCCCACAGG | 10054 |
rs182579641 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34450183 | CAGATTTCATAGTGT[A/G]ATATAGATCAGCAAT | 10054 |
rs182667434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34455192 | ATTAGGATTTTCAAT[A/G]CCTATGTATTCAGAC | 10054 |
rs182697249 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34434215 | CAAATGGGCTCAGGT[A/G]ATACTCTTACCTCAA | 10054 |
rs182701683 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34455560 | TTTATCATTGAAATA[A/T]AAAGACCTGTTTACC | 10054 |
rs183043073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34465568 | TTTGAACCGGGGAGC[C/T]GAGTTTGCAGTGAGC | 10054 |
rs183127274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34465255 | CCAGTTATTTTGTCA[A/G]TATTTTCATGAGTAT | 10054 |
rs183301282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34439408 | AATGCTATACCAGAA[C/T]GTATTGAATGTGGTG | 10054 |
rs183385609 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBA2 | GRCh38.p7 | 19:34442587 | CAGGCGTCTGCCACC[A/G]CGCCCAGCTAATATT | 10054 |
rs183532290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34461702 | ATGACAGGCATAGTT[G/T]TGGGTATTCATAAGT | 10054 |
rs183545638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34459919 | TTCTAGGAAATAATT[A/G]TCTTTGGTATCTCCT | 10054 |
rs183566100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34440023 | ATCTGGGTAAATACA[C/T]TTTTAAAAACTTACT | 10054 |
rs183693912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34456243 | CCTCAGCCTCTCAAG[C/T]AGCTGGGATTACTGG | 10054 |
rs183729405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437141 | TAATTTTTGCATTTT[G/T]GGTAGAGATGAGGTT | 10054 |
rs183870213 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34462241 | GGGATTGAGGGATTT[G/T]TACTAAGGCAGAGGC | 10054 |
rs183876235 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBA2 | GRCh38.p7 | 19:34431678 | GGTTATTTTATAAGT[A/G]TAAAAGTATAATTTT | 10054 |
rs183882344 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBA2 | GRCh38.p7 | 19:34452466 | CATAGAAGTCATAAA[A/G]TCATTTGGAGAAAAC | 10054 |
rs183999753 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34457124 | ACCTGAGATTGGAAG[A/T]TCGAGACTAGCCTGA | 10054 |
rs184018726 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427686 | GGATTACAGGCGCAC[G/T]CCACCACGCCCGGCT | 10054 |
rs184229876 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34449171 | GCCTCCCAGGTTCAA[C/G]CGATTCTCCTGCCTC | 10054 |
rs184230342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446929 | GACTTTCTTATCCCT[A/G]TTGCATTTATTTCCT | 10054 |
rs184275161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34429355 | GGAGATGTTACTGGC[C/T]CTTCGGTGTGAGTTT | 10054 |
rs184282106 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34451270 | GTATTAGGATTAATT[G/T]ATGCACAGCAGTATA | 10054 |
rs184322281 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBA2 | GRCh38.p7 | 19:34437408 | TGAGGTAAGGAGTTC[A/G]AGACCAGCCTGGCCA | 10054 |
rs184393737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34468611 | TCCTGGAAAGCAGAT[A/G]CTCATGTGATCTTCT | 10054 |
rs184412076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446445 | AGACAGGATTTTCGT[C/G]TCTGTCCTGTGTCTC | 10054 |
rs184417768 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34468409 | TAATTTGAAATGTAC[A/G]TTTATTGATTCTCTA | 10054 |
rs184498821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34440658 | CTGGGAATGGGCGCA[A/G]TGTATCATGCCTGTA | 10054 |
rs184940610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467641 | ATTAGCTGGGCGTGG[C/T]AGCATGCGTCTGTAG | 10054 |
rs185037315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34445964 | GTCCGTGTTTTAAAA[G/T]TTTTTTTGTTCTGTC | 10054 |
rs185057796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34439057 | TACTAAAAATACAAA[A/G]ATTAGTTGGCCGTGA | 10054 |
rs185069420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34458321 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 10054 |
rs185076530 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBA2 | GRCh38.p7 | 19:34440994 | AGTGTGTCTTGACCA[C/T]GTGTCTATTCAGGAA | 10054 |
rs185189957 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455943 | ATGAGCCACTGCGCC[C/T]GGCCTTTTTTTTTTA | 10054 |
rs185196166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34463697 | CTGTGTAACTCCTGG[A/G]CTTCAGGAATCAATC | 10054 |
rs185288612 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34459017 | TTCTGAAAAGGTCCA[A/G]CTGCAGAGATGTGTG | 10054 |
rs185295816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436221 | TTGTGAAGTACTTCA[A/G]ACATTTAAATACAAC | 10054 |
rs185316609 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436546 | TCAGGTGATCCACCT[A/G]CCTCGGCCTCCCAAA | 10054 |
rs185539358 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427034 | TTAAATCAATGATAA[C/T]TGCTACAGGACAGTT | 10054 |
rs185710332 | snp | A/G | 9.9126e-05 | 0.0070394 | intron-variant | UBA2 | GRCh38.p7 | 19:34430694 | CATTTCTATAACTTG[A/G]TGGAGCTTCTATTTG | 10054 |
rs185854849 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBA2 | GRCh38.p7 | 19:34451591 | CTTGCTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG | 10054 |
rs186025703 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBA2 | GRCh38.p7 | 19:34464880 | TTTGGGAGGTCGAGG[C/T]GGGTGGATCACCTGA | 10054 |
rs186071677 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBA2 | GRCh38.p7 | 19:34453828 | GCCACCATGCCCAGC[C/T]TAAAACAGTTTTCTT | 10054 |
rs186092915 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34441685 | TTTTTCTTTGGGAGG[C/T]TGAGGTGGGTGAATC | 10054 |
rs186101370 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBA2 | GRCh38.p7 | 19:34464285 | CTGAGTTCCGTGATG[C/T]TTGACCTACAGAAAA | 10054 |
rs186149605 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBA2 | GRCh38.p7 | 19:34442458 | TTTTTTGTTGTTGTT[G/T]TTTTGAGATGGAGTT | 10054 |
rs186155582 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427644 | TGGGTTCAAACGATT[A/C]TCCTGCCTCAGCCTC | 10054 |
rs186164464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34439133 | GAATTGCTTGAACCC[A/G]GGAGGTGGAGGTTGG | 10054 |
rs186350930 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34447304 | TGCTTTTCCCAGTCC[A/G]CTGACTCAAATATTA | 10054 |
rs186749453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442761 | TATAACCTCAATAAA[A/C]CTGTTGTAAAGGTGA | 10054 |
rs186765184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34440045 | AAACTTACTAAGTGC[C/G]CAGTGCGGTGGCTCA | 10054 |
rs186769622 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433946 | CTTGGTGACAGAGTG[C/T]GACCCTGTCTCAAAA | 10054 |
rs186772872 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34455221 | ACCACAAACCTGCAC[A/G]TGCCCTATGTTATTG | 10054 |
rs186812528 | snp | C/T | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34457705 | CCTTTAGAATTCATT[C/T]CTCTTAGCAGACTCA | 10054 |
rs186893819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34429142 | GGGAGACGCAATGGG[A/G]TTGAGTAACTTACCC | 10054 |
rs186901749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34450421 | TATCCTCGCGTAAAG[C/T]CTTTGTATAGCCCTG | 10054 |
rs186918698 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34465466 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 10054 |
rs187020389 | snp | A/G | 4.96093e-05 | 0.00498018 | intron-variant | UBA2 | GRCh38.p7 | 19:34438807 | CTTTTCGGTACTGAT[A/G]ATGGAAAATGGAGTC | 10054 |
rs187027082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34433664 | AGTGAAAAGCTCTCA[A/G]AAAGTGTGACTGTGG | 10054 |
rs187196689 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34454895 | TGGTCATTTTATAGT[A/C]CCCTGTTCAGTCATT | 10054 |
rs187340856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34455658 | TTACTTTTTTTTATC[C/T]TTTGAGACGGAGTCT | 10054 |
rs187468005 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34429562 | AGTAAATGAAATTGT[A/G]TATGGATGAAGGCTT | 10054 |
rs187475452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34451398 | ACTCTAGTAGTGTCC[A/G]CTTACTGAGTTCTCA | 10054 |
rs187560154 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBA2 | GRCh38.p7 | 19:34449280 | TCACCATGTTGGCCA[A/G]GATGGTCTCGATCTC | 10054 |
rs187688031 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34466585 | CTTTTTTATTATAAG[C/T]TCAGTGCTTTGAAAA | 10054 |
rs187713372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443599 | GGCGTGCGCTACCAC[A/G]CCTGGCTAATTTTTA | 10054 |
rs187778662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466296 | AACCGAGATCACGCT[A/G]CTGCACTCTAGCCTG | 10054 |
rs187861004 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34428061 | TTGCCTATATTTTTT[G/T]GGGGGTGACACTTGT | 10054 |
rs187967635 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | UBA2 | GRCh38.p7 | 19:34445449 | ACTTTTTTTTTTTTT[G/T]TTTTTTTGAGATGGA | 10054 |
rs188303302 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467669 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10054 |
rs188399180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34437348 | GGCATGGTGGCTTAC[A/G]CCTGTAATCCCAGCA | 10054 |
rs188457543 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34456296 | ATTTTTGTATTATTA[C/G]TAGAGACGGTGTTTC | 10054 |
rs188526320 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBA2 | GRCh38.p7 | 19:34460138 | ACCCCTGCCATTACA[A/G]GGTTGGCACAGAGAC | 10054 |
rs188541932 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34431787 | TAAGTAGATAACAGC[A/C]TTGTGGCTTCCAGAA | 10054 |
rs188553938 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBA2 | GRCh38.p7 | 19:34453612 | TACTGCAGCCTCTGC[A/G]TCCCGGGTTCAAGTG | 10054 |
rs188579382 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | UBA2 | GRCh38.p7 | 19:34446001 | CCCTAGCAAGTTGTA[C/G/T]GTGTGTGGGGTTTTT | 10054 |
rs188617132 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34435628 | TGAGGTCAGGAGTTC[G/T]AGACCAGCCTCTCCA | 10054 |
rs188667875 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436856 | GAACCTTATTGAATA[C/T]CATTCTACAAAAGAC | 10054 |
rs188797578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34439577 | GCTCATGCCTCTAAT[C/T]CCAGCACTGTGGGAG | 10054 |
rs188952000 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34456077 | CCACTGCACTTGGCC[C/T]GATGCGCTCTTTTTT | 10054 |
rs189202284 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34468422 | ACATTTATTGATTCT[C/G]TACTGTGGGTAGGTT | 10054 |
rs189322823 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469434 | AAAAACCCTTTGAAC[A/G]AAGTGTGTGCATAAC | 10054 |
rs189335655 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441984 | ACACACCTGTAATCC[C/T]GGCTCTTTAGGAGGC | 10054 |
rs189341974 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UBA2 | GRCh38.p7 | 19:34464386 | AACACGGTGAAACCC[C/G]GTCTCTGCTAAAAAT | 10054 |
rs189579403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34457323 | ATTAAGCCGAGATCG[C/T]GCCATTGCACTCCAG | 10054 |
rs189650416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447132 | AAACTGGAGAATTTG[C/G]AGTCTGATGTTTGAG | 10054 |
rs189704638 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34462461 | TGTGTGAAAGGGCTT[C/G]GAGGTGGAAATCTGG | 10054 |
rs189870511 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34439068 | CAAAAATTAGTTGGC[C/T]GTGATGGCGAGTGCC | 10054 |
rs189879907 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34458712 | GAGATTTTAGATTGT[A/G]TGGCGTATAAAATTA | 10054 |
rs189892880 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBA2 | GRCh38.p7 | 19:34437535 | GAATCACTTGAACCC[A/G]GGAGGCAGAGGTTGT | 10054 |
rs190014038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34434035 | GTAATTACTTCCACA[C/T]GTAAAAGTATATCTA | 10054 |
rs190022168 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455284 | TCCACTAAGCACCAA[A/G]TTTAAGATCATTTTT | 10054 |
rs190175073 | snp | C/T | 4.13163e-05 | 0.00454494 | intron-variant | UBA2 | GRCh38.p7 | 19:34464181 | ATTTGAATATATAAA[C/T]TTTAGACAAAATGAA | 10054 |
rs190261590 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427463 | GGTTCAAGCAATTCT[C/G]CTGCCTCAGCCTCCT | 10054 |
rs190311726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438936 | GTAGCTGGCCGGGTG[C/T]GGTGGCTCACACCTG | 10054 |
rs190414638 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34441090 | CTATATAGTTTTCAT[A/T]GATACAGAGAAAGCA | 10054 |
rs190432056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34451611 | GGAGTGCAGTGGCGC[A/G]ATCTTGGCTCACTGC | 10054 |
rs190469286 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465560 | GAGAATTGTTTGAAC[C/T]GGGGAGCCGAGTTTG | 10054 |
rs190573779 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34458017 | GATGTTGATTCTAGA[C/T]AACTGTGAAAGGCAC | 10054 |
rs190672484 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34431006 | GTCCTAGTTGAAACA[A/G]GACAGTTCCCCCGAT | 10054 |
rs190806406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443001 | TATATCCATGAGTTA[C/T]TAAACAGTTTTTAGG | 10054 |
rs190870216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34449371 | CACGCCTGGCCAGAA[A/G]TCCTTACTCAAGGCT | 10054 |
rs190936045 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34449040 | TAAGGAGACTCTTTC[C/T]TTATTTCTTAGATAA | 10054 |
rs190951473 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBA2 | GRCh38.p7 | 19:34428795 | GGCTCCGGACGCCGA[A/G]GAGGCCGCGGGCCCC | 10054 |
rs191118506 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34442476 | TTGAGATGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 10054 |
rs191232426 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34462110 | CTTGTCACATGTGCA[G/T]TGTGTGTCTTCCTCC | 10054 |
rs191276908 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440400 | ATTATTCTAAATAAT[A/G]CACCGAACCTATGTT | 10054 |
rs191280297 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34459048 | GCTGTGATTTCCTGG[C/G]TTATTTTGCCTTCTG | 10054 |
rs191370676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34464938 | AAAGGCTGGTGGTGG[C/T]GCATGCCTGTAATCC | 10054 |
rs191506199 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34439238 | AATGTGGCCATGACT[C/G]TTCAGGAAACTTAGT | 10054 |
rs191735148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34429289 | GTGTACGTTGACAAG[C/T]CAGTGCTATTTTGAA | 10054 |
rs191740945 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | UBA2 | GRCh38.p7 | 19:34457064 | CCGGGCACGATGGCT[C/G]ACACGTGTAATCCCA | 10054 |
rs191744589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34450803 | GCCAAGGCTGGAGCG[C/T]AGTGGCACGATCTCA | 10054 |
rs191782401 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34432804 | AGGTGATCCACCCGC[C/T]TTGGCCTCCCAAAGT | 10054 |
rs191883644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446235 | TATCAAACTGCCTCA[G/T]TATTCTTGCAACTCT | 10054 |
rs191897230 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467693 | AGGCAGGAGGCGGAG[C/G]TTGCAGTGAGCTGGG | 10054 |
rs192030897 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34455004 | TGCTGTCATTTCTGC[C/T]ATTTCTCGTAGTGAT | 10054 |
rs192038497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453852 | TTTTCTTAAATTGCT[C/T]GTCTTTTGGCCTGGA | 10054 |
rs192226423 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427649 | TCAAACGATTCTCCT[A/G]CCTCAGCCTCCCGAG | 10054 |
rs192374884 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34433719 | AATCCCAGCACTTTG[A/C]GAGACCAAGGCAGGA | 10054 |
rs192456595 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34439764 | GGTTGAGGCTGCAGT[G/T]AACCGAGATAGTGCC | 10054 |
rs192564302 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34466304 | TCACGCTACTGCACT[A/C]TAGCCTGGGTGACAG | 10054 |
rs192568735 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBA2 | GRCh38.p7 | 19:34437057 | GTGTTTCAGAGAAAA[C/T]TCTAAATCTGCTGCA | 10054 |
rs192594565 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444019 | ATGTGCTAGGTAATG[C/T]GTGTTTAACATGTGT | 10054 |
rs192693111 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBA2 | GRCh38.p7 | 19:34445717 | TGATGGGATTATAGG[C/T]GTGAGCCACTGCTCC | 10054 |
rs192771925 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462497 | AATGCCAAGGGCATT[C/G]CTGGTAGATTAAAAT | 10054 |
rs192822792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435845 | AAAAAAAAGCCAGGC[A/G]TGATGGCTCATGCCT | 10054 |
rs192906940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467422 | GCAGTGAGCCATGAT[A/T]GCACCACTGCACTGC | 10054 |
rs192975137 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBA2 | GRCh38.p7 | 19:34440890 | GAGATCGCTCTGCTG[C/T]GCTCCAGCCTGGGCA | 10054 |
rs193032000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34455940 | GGCATGAGCCACTGC[G/T]CCCGGCCTTTTTTTT | 10054 |
rs193095222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34451456 | TATTTATCATCTTAT[C/T]TACATTATATCTTCA | 10054 |
rs193116944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34456080 | CTGCACTTGGCCCGA[C/T]GCGCTCTTTTTTTCC | 10054 |
rs193247332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34460182 | GTCAAGTGTGTAGCT[C/T]ACTACCTAACCTGCA | 10054 |
rs193249308 | snp | C/T | 1.65138e-05 | 0.00287343 | intron-variant | UBA2 | GRCh38.p7 | 19:34430541 | TCAAACATACGTAAA[C/T]GTTTGTCATTTATCT | 10054 |
rs199511166 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440308 | ATGAGATGATGTTTC[-/A]AAAAAAAAAAAAAAA | 10054 |
rs199570277 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462736 | TTTGAGGGGCCGAGG[C/T]GGGCAGATCACTTGA | 10054 |
rs199581746 | snp | C/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458829 | CCTTGTGCACTGGAT[C/G]CTCCCAACCCCAATT | 10054 |
rs199614630 | in-del | -/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448528 | TGAGCCCAAGAGGTT[-/G]AGACTTCAGTGAGCT | 10054 |
rs199947318 | snp | A/C | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466974 | TGCCAAAAGCATAAC[A/C]AATGGCAGTGATGAT | 10054 |
rs199949891 | snp | G/T | 0.000132177 | 0.0081284 | intron-variant | UBA2 | GRCh38.p7 | 19:34450253 | TCATGGGATCTGTCT[G/T]TCTTTTGTAAGCTTT | 10054 |
rs199965176 | snp | A/G | 0.00140078 | 0.0264278 | intron-variant | UBA2 | GRCh38.p7 | 19:34443840 | TACTATTCTTAAATT[A/G]TAGCCAGTTGTTTGG | 10054 |
rs200013492 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444049 | TTTTTTTTTTGTTTT[G/T]TTTTTTTTTTTTTTT | 10054 |
rs200021555 | in-del | -/A | 0.0138799 | 0.0821421 | intron-variant | UBA2 | GRCh38.p7 | 19:34431649 | GGTGGTACGTGGGTC[-/A]GGGGGGGCTCTCCGG | 10054 |
rs200180997 | in-del | -/T | 0.0271762 | 0.113356 | intron-variant | UBA2 | GRCh38.p7 | 19:34440649 | AGCATATCCTGGGAA[-/T]TGGGCGCAGTGTATC | 10054 |
rs200218400 | in-del | -/AG | 0.0352966 | 0.128072 | intron-variant | UBA2 | GRCh38.p7 | 19:34465620 | CAGCCTGGGCGACAG[-/AG]GGGGACTCCATGTCA | 10054 |
rs200305854 | snp | A/G | 3.31345e-05 | 0.00407016 | intron-variant | UBA2 | GRCh38.p7 | 19:34454367 | ATGTAAGTTATTTGT[A/G]CTAAAGTTGTATCAC | 10054 |
rs200400594 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436731 | TTGAAACTATAGAAA[C/T]AGAATTATAATGTAC | 10054 |
rs200425158 | snp | A/G | 3.32281e-05 | 0.0040759 | intron-variant | UBA2 | GRCh38.p7 | 19:34433321 | AGGCTAGTTATTTTG[A/G]TGACCTTTTTTTATT | 10054 |
rs200589452 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34462636 | AAATGTTAAAAAGCC[-/A]AAAAAAAAGTGGGGG | 10054 |
rs200624992 | snp | C/T | 1.65081e-05 | 0.00287293 | intron-variant | UBA2 | GRCh38.p7 | 19:34443813 | TAGAATGCTTTGTTA[C/T]ACAGAAGTATTTACT | 10054 |
rs200703133 | snp | C/T | 0.00199798 | 0.0315436 | intron-variant | UBA2 | GRCh38.p7 | 19:34458961 | CTTTTCCTTTTGCTT[C/T]TACAGTATTACTGTG | 10054 |
rs200753160 | snp | A/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452138 | TGGAGCTGAGCTCAT[A/G]TGGGATAAGGTTCGT | 10054 |
rs200763069 | in-del | -/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432567 | GGATTGTGTTTTTTT[-/G]TGTGTGTGAGATAGG | 10054 |
rs200936936 | snp | A/C | 0.000214961 | 0.0103651 | intron-variant | UBA2 | GRCh38.p7 | 19:34468992 | AGGTGAGCACAGGTA[A/C]CTCCCACGCTTTTAC | 10054 |
rs200950535 | snp | C/T | | | missense, synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34464046 | AATCACAAGAAGTTG[C/T]CAGAATTTGGAATTA | 10054 |
rs201018793 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469204 | GAAGAGCTTGATGAT[C/G]TCATAGCATTAGATT | 10054 |
rs201141482 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449443 | TTTGGCTTATTCTCT[A/C]TAAAGATTAAGGATG | 10054 |
rs201201716 | snp | A/G | | | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34443859 | CCAGTTGTTTGGGGA[A/G]GAAGATGCTGATCAA | 10054 |
rs201323741 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34447831 | TTAGGGAGAGGCTTC[A/G]GAAGAGGCTTTCTAG | 10054 |
rs201324122 | snp | A/C/G | 1.65051e-05 | 0.00287267 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452135 | GGATGGAGCTGAGCT[A/C/G]ATATGGGATAAGGTT | 10054 |
rs201336141 | snp | A/T | 9.89699e-05 | 0.00703386 | intron-variant | UBA2 | GRCh38.p7 | 19:34438777 | TTCAAGTAAGAGTGT[A/T]TATTTCTTGGCATGC | 10054 |
rs201402124 | in-del | -/AGGA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465657 | AAAAAAAAAAATGAC[-/AGGA]AGGACTGAATGTGAG | 10054 |
rs201489031 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439993 | ACCATGGTAGTACAT[-/A]AAAAAATTTAAATGA | 10054 |
rs201489973 | snp | A/G | | | missense, synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34464037 | CTAGCTAATAATCAC[A/G]AGAAGTTGTCAGAAT | 10054 |
rs201531113 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436119 | GCGAAACTCTGTCTC[-/A]AAAAAAAAAAAACCA | 10054 |
rs201588428 | snp | C/T | 0.000148455 | 0.00861425 | intron-variant | UBA2 | GRCh38.p7 | 19:34430672 | CAGGTAACTATATTT[C/T]TCATACCATTTCTAT | 10054 |
rs201605897 | in-del | -/CT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449439 | TATGTTTGGCTTATT[-/CT]CTATAAAGATTAAGG | 10054 |
rs201718490 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450767 | TTTTTTTTTTTTTTT[G/T]AGACCGTGTCTCGCT | 10054 |
rs201763124 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446608 | TTGACTTTTTTTTTT[C/T]TTTCTTTTTTTTTTT | 10054 |
rs201872016 | snp | C/G | 0.000759878 | 0.0194772 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34433376 | GTGGAATTTTTCCGA[C/G]AGTTTATACTGGTTA | 10054 |
rs201923928 | snp | C/T | | | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34443851 | AATTATAGCCAGTTG[C/T]TTGGGGAAGAAGATG | 10054 |
rs201934147 | snp | C/T | 4.96348e-05 | 0.00498146 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34467006 | GAGCTCAGCCCTCCA[C/T]CTCCACAGGTGAGTA | 10054 |
rs201971195 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456550 | TTTTAATTTCTAAGA[A/G]CTTTATTTTTTGGTA | 10054 |
rs201995823 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465038 | GCAAAACTCCATCTC[-/A]AAAAAAAAAGGAATT | 10054 |
rs202028900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430538 | AGCTCAAACATACGT[A/T]AACGTTTGTCATTTA | 10054 |
rs202044629 | snp | G/T | 0.499563 | 0.0147699 | intron-variant | UBA2 | GRCh38.p7 | 19:34444044 | ATGTGTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 10054 |
rs202061411 | snp | A/C | 0.000297074 | 0.012184 | intron-variant | UBA2 | GRCh38.p7 | 19:34450262 | CTGTCTTTCTTTTGT[A/C]AGCTTTTTAAAGATG | 10054 |
rs202104692 | in-del | -/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427096 | TGCACAATTTTAGGG[-/T]TTTTTTTTTCTTTTT | 10054 |
rs202233619 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455531 | ATACTTTGACTGTTG[C/T]TTAGGTTCTCCTTTT | 10054 |
rs367630035 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439284 | GCCATGTAACTAAGC[A/G]ATAAAAATCTTTATA | 10054 |
rs367637106 | snp | C/G/T | 3.29464e-05 | 0.00405861 | missense, synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452087 | TTTTTCAAAGAGCAT[C/G/T]GAGACTTTGAGAGTT | 10054 |
rs367661213 | snp | C/T | 0.000247776 | 0.0111277 | intron-variant | UBA2 | GRCh38.p7 | 19:34438797 | TCTTGGCATGCTTTT[C/T]GGTACTGATGATGGA | 10054 |
rs367685499 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452113 | GAGTTCATTTAGCAG[A/G]AAAGGGGGATGGAGC | 10054 |
rs367799623 | snp | C/T | | | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470329 | TATTCTTGGAGACTT[C/T]ACATGTAGGAAGAGT | 10054 |
rs367810317 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436361 | CTGCAGTGCAGTGGC[A/G]CGATCTCAGCTCGCC | 10054 |
rs367814984 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461184 | AGTTGCTGTTCTCGT[G/T]TTTTCCATGTCCCAG | 10054 |
rs367832807 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444378 | GTTTTACAAAAAAAA[A/T]ATGATTCCGTTTTAC | 10054 |
rs367861772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453953 | GTGGAATTGAGATTC[C/T]GGTGTATACAACTGA | 10054 |
rs367907859 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBA2 | GRCh38.p7 | 19:34429048 | AGCGGGTTTACACAC[A/G]GAACGCGCACCATCT | 10054 |
rs367942960 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439622 | ATCCCTTGAGCCCAG[A/G]AGTTTGAGACCAGCC | 10054 |
rs368142349 | snp | C/T | 3.44092e-05 | 0.0041477 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34451990 | CTTTAGGAGAAGAAA[C/T]GAATGCATCAGATCA | 10054 |
rs368195664 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469848 | TAAAACTCAAATAAC[A/G]ACTATACTTATGGAC | 10054 |
rs368314356 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434672 | AGTAAATTTGTGATA[C/T]AAATTCTATTTGATA | 10054 |
rs368357335 | snp | A/G | | | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428441 | TCCCGCCATGGCACT[A/G]TCGCGGGGGCTGCCC | 10054 |
rs368418143 | snp | C/T | 0.000126968 | 0.00796667 | intron-variant | UBA2 | GRCh38.p7 | 19:34451938 | ACAGTAGAGGAATGA[C/T]GTTAATTAGTGAAAT | 10054 |
rs368418442 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434846 | TTTTCCCAAAAACTC[A/T]TACTGTTTGTTTTAC | 10054 |
rs368523604 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467280 | GGAGAACAGCCTGGG[C/G/T]AACACAATGAGAGAC | 10054 |
rs368559860 | snp | G/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427537 | TCGGTGTTTTTTTTT[G/T]TTTGTTTGTTTGTTT | 10054 |
rs368568014 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456078 | CACTGCACTTGGCCC[C/G]ATGCGCTCTTTTTTT | 10054 |
rs368571970 | snp | A/C/G | 0.000297478 | 0.0121924 | intron-variant | UBA2 | GRCh38.p7 | 19:34450392 | TTTTAGTCTTGGAAC[A/C/G]CCTAAGCTGGAAATA | 10054 |
rs368630600 | in-del | -/AATG | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453507 | TTTTTCTGAAGTGTT[-/AATG]AAACAGCTTTTTTTT | 10054 |
rs368660163 | snp | A/C | 0.000296888 | 0.0121801 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445094 | GGCTAAATCAACTGG[A/C]TATGATCCAGTTAAA | 10054 |
rs368776373 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34448728 | GTGGTTTTGTAGATA[A/G]GTAGAGAGGTTTCAA | 10054 |
rs368785614 | snp | A/G | 0.000777053 | 0.0196958 | intron-variant | UBA2 | GRCh38.p7 | 19:34464141 | TCATAGGTAAGAGCT[A/G]TTAGTATTTTAATTG | 10054 |
rs368870624 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437620 | TCTCAGACAAAAAGA[A/G]AAAAAGAAGAGACTG | 10054 |
rs368891384 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34463304 | CCCCTGAAGTAGTTT[C/T]GGTAGTTAAGTGTTT | 10054 |
rs368940126 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34468195 | TCTTTGTTTTCATTT[A/C]TTTGACCCTATGTCT | 10054 |
rs369045629 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449165 | CTCTCCGCCTCCCAG[A/G]TTCAAGCGATTCTCC | 10054 |
rs369048863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441811 | CTGTAGTCCCACCTA[C/T]TCGGGAGGCTGAGCC | 10054 |
rs369051088 | snp | C/T | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467704 | GGAGGTTGCAGTGAG[C/T]TGGGATCGCGCCACT | 10054 |
rs369080841 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442584 | TTACAGGCGTCTGCC[A/C]CCACGCCCAGCTAAT | 10054 |
rs369094219 | in-del | -/TTTGTTTG | 0.00358779 | 0.0422022 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427534 | GTTTCGGTGTTTTTT[-/TTTGTTTG]TTTGTTTGTTTGTTT | 10054 |
rs369166559 | snp | C/T | 5.15477e-05 | 0.00507653 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469073 | TTCTCATAGTTGATT[C/T]AGATGAAGAAGATTC | 10054 |
rs369174176 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432253 | GACTTTTCTAAAGTG[A/T]TTGCCTTTTTTTGTT | 10054 |
rs369184752 | in-del | -/TTTC | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456103 | TTTTTTCCTTTTCTT[-/TTTC]TTTTTTTTTTTTTTT | 10054 |
rs369345407 | snp | A/G | 1.68624e-05 | 0.0029036 | intron-variant | UBA2 | GRCh38.p7 | 19:34454419 | TAAACAGTGAAACAT[A/G]CTCATCCTTTTTTTT | 10054 |
rs369372775 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34456863 | GTTCCTGGCCGATAC[C/T]CAGTTTTTAAATTAT | 10054 |
rs369413823 | in-del | -/TG | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444043 | CATGTGTTTTTTTTT[-/TG]TTTTTTTTTTTTTTT | 10054 |
rs369462476 | snp | A/G | 3.29957e-05 | 0.00406162 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466897 | GACCTAGGAAAGGAC[A/G]TTGAATTTGAAGTTG | 10054 |
rs369582790 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34431570 | TAAGTGAATGAATGA[A/T]TGACACTTGGTTACT | 10054 |
rs369593839 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34455815 | TGCCGGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 10054 |
rs369635309 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34441160 | TTCTACTAAAACAGA[A/G]TAAAAACTTACTAGG | 10054 |
rs369767486 | snp | G/T | 1.68238e-05 | 0.00290028 | intron-variant | UBA2 | GRCh38.p7 | 19:34454223 | CAAAATAGTCAATTT[G/T]TGGAGAAACTTGTTA | 10054 |
rs369768394 | snp | C/T | 0.000193981 | 0.00984647 | intron-variant | UBA2 | GRCh38.p7 | 19:34454208 | CTGAAAGTAATGCTT[C/T]AAAATAGTCAATTTG | 10054 |
rs369832495 | in-del | -/G | 0.000568505 | 0.0168502 | intron-variant | UBA2 | GRCh38.p7 | 19:34460466 | CTTTTTTTTTTTTTT[-/G]TAGATAGTGAAAGAA | 10054 |
rs369860031 | in-del | -/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444044 | ATGTGTTTTTTTTTT[-/G]TTTTTTTTTTTTTTT | 10054 |
rs370032824 | snp | A/G | 0.000161987 | 0.00899818 | missense, synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428562 | ACCGGTTTCTCCCAC[A/G]TCGACCTGGTGAGGG | 10054 |
rs370076230 | in-del | -/GA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436323 | TATTTTTTTGAGACA[-/GA]ATTTCGCTCTTGTTG | 10054 |
rs370102677 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431239 | TTTTCCTATCATTTT[C/T]TTTTCTTTTTTTTTT | 10054 |
rs370186723 | snp | C/T | 0.000268007 | 0.0115729 | intron-variant | UBA2 | GRCh38.p7 | 19:34444968 | GTTCTACATTTATTA[C/T]GGTTGAAAATAAAAT | 10054 |
rs370201433 | snp | C/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426776 | ACACTCCCAGCCATG[C/T]TCAGACATGCTCTGC | 10054 |
rs370208270 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451778 | GTCTCGATCTCCTGA[C/T]CTCATGATCCGTCTG | 10054 |
rs370234655 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429852 | AAAAACAAAGAAAAA[A/G]AACAGGGCATAGTTA | 10054 |
rs370239818 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458517 | AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 10054 |
rs370277115 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446336 | ACTGTTCCACATAAC[C/T]GAAAACTCTTTTTCT | 10054 |
rs370384328 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34450864 | CCCGCCTCAGCCTCC[C/T]GAGTAGCTGGGATAA | 10054 |
rs370428515 | snp | A/G | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467425 | GTGAGCCATGATTGC[A/G]CCACTGCACTGCAGC | 10054 |
rs370585686 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469758 | GTTTTCAGTTTGTAC[C/T]GCCTGGTATGTCTGT | 10054 |
rs370610578 | snp | A/G | 3.29979e-05 | 0.00406175 | intron-variant | UBA2 | GRCh38.p7 | 19:34443928 | TGAGTAAATTATTTG[A/G]CATATGTTTTATCAG | 10054 |
rs370693302 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450800 | GTTGCCAAGGCTGGA[A/G]CGCAGTGGCACGATC | 10054 |
rs370737941 | snp | C/T | 6.639e-05 | 0.00576113 | intron-variant | UBA2 | GRCh38.p7 | 19:34433438 | TTTAATACTTTTAAT[C/T]TCTCAGTATTTCCTC | 10054 |
rs370760032 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466126 | GGATCACAGGCTCAG[C/G]GGTTCAAAACCAGCC | 10054 |
rs370809433 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461598 | AACTGGTCAGGAATT[-/T]TCAGTGGCTTCAGCG | 10054 |
rs370848936 | snp | A/G | 1.65269e-05 | 0.00287457 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34433374 | ATGTGGAATTTTTCC[A/G]ACAGTTTATACTGGT | 10054 |
rs370956996 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436734 | AAACTATAGAAAGAG[A/T]ATTATAATGTACTTA | 10054 |
rs371017623 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBA2 | GRCh38.p7 | 19:34450398 | TCTTGGAACACCTAA[A/G]CTGGAAATATCCTCG | 10054 |
rs371117030 | snp | A/T | | | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470092 | AAACCCCATCTCTAC[A/T]AAAAAAAAAAAAAAA | 10054 |
rs371121000 | snp | C/G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439162 | GGAGTGAGCCGAGAT[C/G/T]GCGCCACTGCACTCC | 10054 |
rs371206459 | snp | A/C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433919 | GCCTAGATCACACCA[A/C/T]TACACTCCAGCCTTG | 10054 |
rs371214021 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436386 | CTCGCCGCAACCTCC[A/G]TCTCCCTGGTTCAAG | 10054 |
rs371228240 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34461254 | CCTGTGTTTCCCTGT[A/G]TATTGACTTAATTCA | 10054 |
rs371247982 | snp | A/C | 0.000140463 | 0.00837925 | missense, intron-variant | UBA2 | GRCh38.p7 | 19:34460470 | TTTTTTTTTTTGTAG[A/C]TAGTGAAAGAAAAAT | 10054 |
rs371323093 | snp | C/G | 3.29478e-05 | 0.00405867 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452103 | GAGACTTTGAGAGTT[C/G]ATTTAGCAGAAAAGG | 10054 |
rs371341626 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440051 | ACTAAGTGCCCAGTG[C/T]GGTGGCTCAGGCCTG | 10054 |
rs371342060 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466295 | GAACCGAGATCACGC[A/T]ACTGCACTCTAGCCT | 10054 |
rs371361702 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432561 | TATCTCCGGATTGTG[G/T]TTTTTTTGTGTGTGA | 10054 |
rs371440022 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453958 | ATTGAGATTCCGGTG[G/T]ATACAACTGAGTCTC | 10054 |
rs371473368 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462296 | AGTCAGAACTTGGAG[C/T]CCAGTTGAGGAATAG | 10054 |
rs371487963 | snp | A/G | 4.96077e-05 | 0.0049801 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445109 | ATATGATCCAGTTAA[A/G]CTTTTTACCAAGGTT | 10054 |
rs371532954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34432014 | TCATTCAGCTTTTTT[A/T]AAAAAAATGATTTTT | 10054 |
rs371661388 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467017 | TCCACCTCCACAGGT[C/G]AGTATGGCCCCAGCC | 10054 |
rs371821866 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34429855 | AACAAAGAAAAAGAA[A/C]AGGGCATAGTTAAAT | 10054 |
rs371847510 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435554 | CTTTGTGTCGGCTGC[A/G]TGCAGTGGCTCATGC | 10054 |
rs371909636 | snp | C/G | 3.57494e-05 | 0.0042277 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469045 | CTGAAATAAGCTCAA[C/G]AGCAAGATGACGTTC | 10054 |
rs371914789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467287 | AGCCTGGGCAACACA[A/G]TGAGAGACCCCCATC | 10054 |
rs371941376 | in-del | -/TCAG | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427745 | GTTTCACCATGTTAG[-/TCAG]GCTGGTTTCAGAACT | 10054 |
rs372015863 | snp | G/T | 1.64953e-05 | 0.00287182 | intron-variant | UBA2 | GRCh38.p7 | 19:34443834 | AGTATTTACTATTCT[G/T]AAATTATAGCCAGTT | 10054 |
rs372039082 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443514 | TTGTGCAGTCTCGGC[C/T]CACTGCAACCTCCAT | 10054 |
rs372280176 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439494 | AAATCTTTACTAAGA[A/G]TCCAATTTAAGTTAG | 10054 |
rs372385389 | snp | C/T | 0.000347852 | 0.0131835 | intron-variant | UBA2 | GRCh38.p7 | 19:34460434 | ATCTTTAATTACCTA[C/T]GTTAATATTTTGAAT | 10054 |
rs372427517 | snp | C/G/T | 0.000159409 | 0.00892653 | intron-variant | UBA2 | GRCh38.p7 | 19:34434997 | TTATTTTTTTAACTT[C/G/T]CCAAATATTTATTTG | 10054 |
rs372478455 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436765 | ACATTTGCTGGTTGC[A/G]TCTAATTTTTTTTGG | 10054 |
rs372482233 | in-del | -/GTTTATTT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436305 | TTTATTTATTTATTT[-/GTTTATTT]TTTTGAGACAGAATT | 10054 |
rs372502923 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | UBA2 | GRCh38.p7 | 19:34458747 | ACGTTTCCGATTTCT[G/T]CCTGTTATTTCTCCT | 10054 |
rs372610736 | snp | A/G | 1.6546e-05 | 0.00287624 | intron-variant | UBA2 | GRCh38.p7 | 19:34430705 | CTTGATGGAGCTTCT[A/G]TTTGTGATACCAGAT | 10054 |
rs372786949 | snp | G/T | 0.000307953 | 0.0124049 | intron-variant | UBA2 | GRCh38.p7 | 19:34454427 | GAAACATACTCATCC[G/T]TTTTTTTTTTTCCCA | 10054 |
rs372890700 | snp | G/T | 1.86121e-05 | 0.00305052 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469253 | ACAGAACCCTCTTAC[G/T]ATTTAGTTTATCTGG | 10054 |
rs372909073 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441928 | TGTGTCTCAGAAAAA[A/G]ACAAAAAAAAAAAAA | 10054 |
rs373018210 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440208 | GGGCATCTGTAGTCC[C/T]AGCTACTTGGGAGAC | 10054 |
rs373034867 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450154 | CTGCTGGTATATGAC[A/G]TGTATCTTTAAATCA | 10054 |
rs373134964 | snp | C/G | 0.00224741 | 0.0334463 | intron-variant | UBA2 | GRCh38.p7 | 19:34454235 | TTTGTGGAGAAACTT[C/G]TTAAATTGTTTAAAT | 10054 |
rs373266979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34458518 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 10054 |
rs373339650 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBA2 | GRCh38.p7 | 19:34432507 | GTCCTTGTTTGAGGT[A/G]CTGGAATTGAGGTAC | 10054 |
rs373366404 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465909 | ACCCCTTAAAACGTG[C/T]GTCTTTTGTTTGACT | 10054 |
rs373446295 | snp | C/T | | | intron-variant, upstream-variant-2KB | PDCD2L, UBA2 | GRCh38.p7 | 19:34426332 | CAGCTGTCACAGTGG[C/T]AGCTAGGAAGGTAGC | 10054 |
rs373522401 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UBA2 | GRCh38.p7 | 19:34443074 | AATTGTTTGTTAACA[C/G]TCTGTTCAGCAGTAA | 10054 |
rs373529655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430859 | AAAGGAAATAATCCC[G/T]TGATGGTGTAACTTT | 10054 |
rs373551149 | snp | A/G | 3.3184e-05 | 0.00407319 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34464074 | TTAGAAATGGCAGCC[A/G]GCTTCAAGCAGATGA | 10054 |
rs373607806 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445034 | AGCCAGAGCTAGAGC[A/G]TCTAATGAAGATGGT | 10054 |
rs373624001 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440144 | GCCTGGCCAACATGG[C/T]GAAACCCCGTCTCTA | 10054 |
rs373628593 | in-del | -/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437699 | GAAAAGTTGTCTCAG[-/G]TGTCATGTACTTCTT | 10054 |
rs373842077 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466297 | ACCGAGATCACGCTA[C/G]TGCACTCTAGCCTGG | 10054 |
rs373852960 | snp | A/G | 4.94181e-05 | 0.00497057 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34438685 | ATCCTAAGCCGACCC[A/G]GAGAACCTTTCCTGG | 10054 |
rs373864253 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | UBA2 | GRCh38.p7 | 19:34456889 | ATTATTTAAAAAAAA[A/T]TTTTTATAGCAGCCT | 10054 |
rs373876679 | snp | C/T | 2.43466e-05 | 0.00348894 | intron-variant | UBA2 | GRCh38.p7 | 19:34428587 | TGAGGGCCGGGCGCG[C/T]GCGCGTGAATGGCGG | 10054 |
rs373883131 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431244 | CTATCATTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 10054 |
rs373952279 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34435976 | AAATACAAAAATCAG[C/T]GGGCGTGGTGGTGTG | 10054 |
rs373954591 | snp | A/G | 1.65187e-05 | 0.00287386 | intron-variant | UBA2 | GRCh38.p7 | 19:34443939 | TTTGGCATATGTTTT[A/G]TCAGATACTATTATC | 10054 |
rs373992899 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457539 | ATCAAACAAATCTTT[C/T]TCCCTCTGTAGCCTG | 10054 |
rs374012482 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444100 | TTCTCTCTTATTGCC[A/C]AGGCTGGAGTACAAT | 10054 |
rs374404738 | snp | C/T | 4.94189e-05 | 0.00497062 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431892 | TACTGCAGTTTTACC[C/T]GAAAGCTAATATCGT | 10054 |
rs374413626 | snp | A/G | 6.446e-05 | 0.00567678 | intron-variant | UBA2 | GRCh38.p7 | 19:34451930 | AACAGAGCACAGTAG[A/G]GGAATGATGTTAATT | 10054 |
rs374462233 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBA2 | GRCh38.p7 | 19:34454219 | GCTTCAAAATAGTCA[A/G]TTTGTGGAGAAACTT | 10054 |
rs374501995 | snp | C/T | 5.18121e-05 | 0.00508954 | intron-variant | UBA2 | GRCh38.p7 | 19:34435016 | AATATTTATTTGAGA[C/T]CTTGGAGCAGGAGGA | 10054 |
rs374545198 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443070 | TTCAAATTGTTTGTT[A/G]ACACTCTGTTCAGCA | 10054 |
rs374822071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467210 | TGGTGGCTTACACCT[A/G]TAATCCCAGCACTTT | 10054 |
rs374837615 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466190 | AATACAAAAAAATTA[G/T]CCAGGTGTGGTGGCG | 10054 |
rs374860259 | snp | C/G | 4.9812e-05 | 0.00499034 | intron-variant | UBA2 | GRCh38.p7 | 19:34464021 | AAATTATTCACGTTT[C/G]CTAGCTAATAATCAC | 10054 |
rs374959938 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444033 | TGTGTTTAACATGTG[-/T]TTTTTTTTTTGTTTT | 10054 |
rs375062800 | snp | C/T | 4.9579e-05 | 0.00497866 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452016 | GATCAACAGAATGAA[C/T]CCCAGTTAGGCCTGA | 10054 |
rs375155901 | snp | A/C/G | 3.31473e-05 | 0.00407096 | intron-variant | UBA2 | GRCh38.p7 | 19:34454370 | TAAGTTATTTGTACT[A/C/G]AAGTTGTATCACTAA | 10054 |
rs375236348 | snp | C/T | 0.000135736 | 0.00823708 | intron-variant | UBA2 | GRCh38.p7 | 19:34464143 | ATAGGTAAGAGCTAT[C/T]AGTATTTTAATTGTA | 10054 |
rs375271639 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460298 | GATGTGGGGATGGAA[C/T]TCAGGTGAATCCCCA | 10054 |
rs375300698 | snp | C/G | 3.29794e-05 | 0.00406061 | intron-variant | UBA2 | GRCh38.p7 | 19:34430559 | TTGTCATTTATCTGG[C/G]GTTTATGCATTTGTA | 10054 |
rs375309736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34455749 | CCCAGGATCAAGCGA[C/T]TCTCCTGTCTCAGCC | 10054 |
rs375344765 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445326 | AATCTATCAGTATAA[C/T]ATCTAAATAGGAGGT | 10054 |
rs375420907 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34461562 | TGTAGCCAGCTCTTT[C/T]AAATGCTAGCTTAAA | 10054 |
rs375473299 | snp | A/G/T | 0.000211111 | 0.010272 | intron-variant | UBA2 | GRCh38.p7 | 19:34450413 | GCTGGAAATATCCTC[A/G/T]CGTAAAGTCTTTGTA | 10054 |
rs375509171 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438092 | AATAAAATGAAGAGT[A/G]TTTGGTTTAGTAACA | 10054 |
rs375532426 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461220 | GCCAGTGTACTGTTA[C/T]TTTCGAAGGTTTCTA | 10054 |
rs375664377 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461352 | CTTCTTTAAATTCAG[A/G]TTTAGTGTCAAGGTT | 10054 |
rs375679781 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436921 | TAAGTGGAGGCCTTC[A/G]GTATCTGTTGACAGA | 10054 |
rs375735319 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34459801 | TGCCTGATAGGGAAT[A/G]GCCTTTCTTCCAGAA | 10054 |
rs375837895 | snp | A/G | 4.63102e-05 | 0.00481175 | intron-variant | UBA2 | GRCh38.p7 | 19:34460576 | CGGAAGGTATCATAC[A/G]TTGTATTTATTCATT | 10054 |
rs375875721 | snp | A/C | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426771 | TAAAAACACTCCCAG[A/C]CATGTTCAGACATGC | 10054 |
rs375895040 | snp | C/G | 1.65211e-05 | 0.00287407 | intron-variant | UBA2 | GRCh38.p7 | 19:34443943 | GCATATGTTTTATCA[C/G]ATACTATTATCTTTA | 10054 |
rs375967858 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34439229 | AAAAAAAAAAATGTG[A/G]CCATGACTGTTCAGG | 10054 |
rs376022812 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428309 | GGCGCGATGTGCCCT[A/G]CCTGTGTCTGCCGGA | 10054 |
rs376026866 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453091 | TAAGACAGCTGCTTA[C/G]GGAAGACACTGTGTT | 10054 |
rs376065237 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441930 | TGTCTCAGAAAAAGA[A/C]AAAAAAAAAAAAAAG | 10054 |
rs376143289 | snp | C/T | 3.36564e-05 | 0.00410208 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469101 | TTCTTCAAATAATGC[C/T]GACGTCAGTGAAGAA | 10054 |
rs376168855 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433802 | GTCTCTACCAAAAAA[C/T]ACAAAAATTAGCCGG | 10054 |
rs376182291 | snp | C/G | 5.32931e-05 | 0.00516175 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469048 | AAATAAGCTCAAGAG[C/G]AAGATGACGTTCTCA | 10054 |
rs376186295 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34459248 | TTGACAAATAACAGG[G/T]ATCCTTGAATGGTCC | 10054 |
rs376261393 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34454490 | TACTACTAATGCAGT[A/G]ATTGCTGGGTTGATA | 10054 |
rs376401493 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426488 | ACTCCAGTGCTTCCT[A/G]TGCTGTTTCTGGCAC | 10054 |
rs376520662 | snp | C/T | 0.000265239 | 0.011513 | intron-variant | UBA2 | GRCh38.p7 | 19:34433433 | GTTATTTTAATACTT[C/T]TAATTTCTCAGTATT | 10054 |
rs376561637 | in-del | -/GTA | 0.00398564 | 0.0444627 | intron-variant | UBA2 | GRCh38.p7 | 19:34464693 | AGAGGCAAATTCATT[-/GTA]GTAATTAAACTGGAA | 10054 |
rs376604349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34462511 | TCCTGGTAGATTAAA[A/G]TGGTAAAGCAAGCAA | 10054 |
rs376732789 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445524 | GGCTCACTGCAGCCC[C/T]GCCTCCTGGGTTCAA | 10054 |
rs376746661 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463901 | TGGGGATTAGGGTTT[A/C]AACCTTTGGATTTTG | 10054 |
rs376764765 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436733 | GAAACTATAGAAAGA[A/G]AATTATAATGTACTT | 10054 |
rs376775466 | snp | A/G | 3.3432e-05 | 0.00408838 | intron-variant | UBA2 | GRCh38.p7 | 19:34452189 | ACTTACATGTCAAAA[A/G]TGTGTTTTAGTTCTT | 10054 |
rs376805929 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438820 | ATGATGGAAAATGGA[A/G]TCATTTTTATTTAAT | 10054 |
rs376864265 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456862 | CGTTCCTGGCCGATA[A/C]CCAGTTTTTAAATTA | 10054 |
rs377067934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442535 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCTCAG | 10054 |
rs377126767 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451634 | CTCACTGCAAGCTCC[G/T]CCTCCCGGGTTCGCG | 10054 |
rs377179804 | in-del | -/AGA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437628 | AAAAAGAAAAAAAGA[-/AGA]GACTGAGGTTAGGAA | 10054 |
rs377184164 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431841 | ATATTGTAGTAATTC[A/C]GTGTTGTTTATTTTT | 10054 |
rs377324716 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34443850 | AAATTATAGCCAGTT[A/G]TTTGGGGAAGAAGAT | 10054 |
rs377391075 | snp | C/G/T | 3.29674e-05 | 0.00405988 | intron-variant | UBA2 | GRCh38.p7 | 19:34431813 | CAGAAGCAGATTTCA[C/G/T]ATAGGAACAGAAATA | 10054 |
rs377497573 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBA2 | GRCh38.p7 | 19:34437379 | CTTTGGGAGGCCAAG[A/G]CGGGCGGATCACCTG | 10054 |
rs377502848 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463032 | AACCTGGGAGGTGGA[A/G]GTTGCAGTGAGCCAA | 10054 |
rs377504211 | snp | C/T | 3.31868e-05 | 0.00407336 | intron-variant | UBA2 | GRCh38.p7 | 19:34458755 | GATTTCTGCCTGTTA[C/T]TTCTCCTCCAAAGAT | 10054 |
rs377504724 | snp | A/T | 8.27164e-05 | 0.0064305 | intron-variant | UBA2 | GRCh38.p7 | 19:34433420 | TAACAGAGGTGAGGT[A/T]ATTTTAATACTTTTA | 10054 |
rs377635921 | snp | A/G | 5.22507e-05 | 0.00511103 | intron-variant | UBA2 | GRCh38.p7 | 19:34460598 | TTATTCATTCCTCTC[A/G]TTGAGGAGACTGCTT | 10054 |
rs377669218 | snp | A/G | 1.66977e-05 | 0.00288939 | intron-variant | UBA2 | GRCh38.p7 | 19:34431939 | ATCATGAAGTATGCT[A/G]TAGTGATTACATTGC | 10054 |
rs377672190 | snp | A/G | 4.88591e-05 | 0.00494239 | intron-variant | UBA2 | GRCh38.p7 | 19:34428590 | GGGCCGGGCGCGCGC[A/G]CGTGAATGGCGGGCT | 10054 |
rs377689576 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443175 | TGCACCTGAGGTATA[A/C/T]AATAATGTTTGTTGA | 10054 |
rs377704677 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34433840 | GCATGTGCCTGTAGT[C/T]CCAGCTTCTCCGGAG | 10054 |
rs377734369 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBA2 | GRCh38.p7 | 19:34437769 | ATGTGTATCAATAAA[A/G]TGGGCTGGGCGCAGT | 10054 |
rs386365543 | in-del | -/T | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34432568 | GATTGTGTTTTTTTT[-/T]GTGTGTGAGATAGGG | 10054 |
rs397694704 | in-del | -/A | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34438236 | AAAAAAAAAAAAAAA[-/A]CACATATAAGAAAAT | 10054 |
rs397733501 | in-del | -/A | 0 | 0 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470109 | AAAAAAAAAAAAAAA[-/A]TTAGCCGGGCCTGGT | 10054 |
rs397770783 | in-del | -/A | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34465652 | AAAAAAAAAAAAAAA[-/A]TGACAGGAAGGACTG | 10054 |
rs397859438 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444068 | TTTTTTTTTTTTTTT[-/T]GTCTCAGAGGTGGAG | 10054 |
rs397945177 | in-del | -/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449337 | CTCCCAAAGTGCTGG[-/G]ATTACAGGTGTGAGC | 10054 |
rs398034431 | in-del | -/A | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34441944 | CAAAAAAAAAAAAAA[-/A]GATAATGTGGCCAGG | 10054 |
rs398034433 | in-del | -/A | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34464571 | TTAAAAAAAAAAAAA[-/A]GAAAACCAGAAATAA | 10054 |
rs398040976 | in-del | -/A | 0.5 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34439207 | GTGAGAATTTGTCTC[-/A]AAAAAAAAAAAAAAA | 10054 |
rs398052695 | snp | C/G | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427685 | GGGATTACAGGCGCA[C/G]GCCACCACGCCCGGC | 10054 |
rs527269157 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450482 | ATTCAAACAGTGCAA[A/G]AAAATATGAAGAACA | 10054 |
rs527277931 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBA2 | GRCh38.p7 | 19:34451735 | GTATTTTTAGTAGAG[A/G]CGGGGTTTCACCATG | 10054 |
rs527286806 | snp | C/T | 4.2311e-05 | 0.00459932 | intron-variant | UBA2 | GRCh38.p7 | 19:34450412 | AGCTGGAAATATCCT[C/T]GCGTAAAGTCTTTGT | 10054 |
rs527314161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34464994 | AGTGAGCCAAGATTG[C/T]GTCATTGCACTCCAG | 10054 |
rs527331849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34448442 | TCTAAAAACGAAAAA[A/G]AAATAGCCAGCCATG | 10054 |
rs527353752 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445911 | TGTGAAATTGTTTTT[A/G]TTGGGTCTACCTAAT | 10054 |
rs527356813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465325 | CTACATTTCATACTT[C/T]GTTTATAAAAAGCAT | 10054 |
rs527474219 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34437618 | CGTCTCAGACAAAAA[A/G]AAAAAAAGAAGAGAC | 10054 |
rs527504553 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34437195 | TCAAACTCCTGACCT[C/G]AGGTGATCCGCCTGC | 10054 |
rs527546131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34450897 | GGTGTGAGCCACTGC[A/G]CCTAGCCTATTTATG | 10054 |
rs527664616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466613 | AAATTAGAATCCAAG[A/G]TGGGTATGGTTGGCT | 10054 |
rs527671621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34458529 | TTGCGCCACTGCACT[C/G]CAGCCTGGGCGACAG | 10054 |
rs527681646 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433938 | ACTCCAGCCTTGGTG[A/G]CAGAGTGCGACCCTG | 10054 |
rs527700701 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34431655 | ACGTGGGTCAGGGGG[G/T]GCTCTCCGGTTATTT | 10054 |
rs527726551 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34466154 | GCCTAGCCAATATGG[G/T]GAAACCCTGTCTCTA | 10054 |
rs527812218 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34431083 | ACATCTTTTCCCTTT[G/T]CCTGTCTCCCAACCT | 10054 |
rs527818979 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439967 | ATAAGAAAAAAAAGG[A/G]ATGATAATAAGACCA | 10054 |
rs527873812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442420 | TCATAAATAAAAAAT[A/G]CCATTAAGTAAAAAA | 10054 |
rs527886125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34444736 | GGCTTGAGCCCAAGA[A/G]GTAGAAGCTACAGTG | 10054 |
rs528050913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34432767 | ATCATGTTGGCCAGG[C/G]TGGTCTCAAACTCCC | 10054 |
rs528088675 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBA2 | GRCh38.p7 | 19:34466537 | AAGTGCATGTAGAGT[C/T]TTTGATTATCACAGA | 10054 |
rs528113826 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34439016 | GAGTTTGAGACCAGC[A/G]TGGCCAGCATGGTGA | 10054 |
rs528280495 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34468500 | GTTGGACGAGGAGAT[A/C]AAACCACCTTTAGTA | 10054 |
rs528440984 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34433235 | TATGACATATAATCC[A/T]GATATCAGTTTTGTT | 10054 |
rs528454044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435106 | TGCTTATATAAAACT[G/T]AAAATGCGGGGCCAG | 10054 |
rs528497302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34454838 | AAGATGTTTCAACTG[G/T]TTTTCAATTCTGAGA | 10054 |
rs528548204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453954 | TGGAATTGAGATTCC[A/G]GTGTATACAACTGAG | 10054 |
rs528569795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34461872 | TTCAGCTTTGTGAAA[C/T]GGAGGGGGAGTAATA | 10054 |
rs528620018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34435173 | GAGGCCGAGGTGGGC[A/G]GATCACCTGAGGTCA | 10054 |
rs528679183 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449218 | GGGATTACAGGCACG[C/T]GCCACGACGCCCAGC | 10054 |
rs528680665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34441177 | AAAAACTTACTAGGC[C/T]GGGCGAGGTGGCTCA | 10054 |
rs528683655 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34435384 | GCCTGGGCTACAGAT[-/C]AAGCCTCTGTCTCAA | 10054 |
rs528819191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447691 | AGATGAGAAGTCAAA[C/T]TTTGAACAATAAATT | 10054 |
rs528870972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438338 | TCCAGTAGTTTTTCT[G/T]TTTAGTGTGATCAAG | 10054 |
rs529099485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34432660 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGTCTCA | 10054 |
rs529213939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438983 | GGAAACTGAGGTGGT[C/T]GGATCACCTGAGCGC | 10054 |
rs529310976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453136 | CTTAGTCCTCACCAC[A/T]CCTTATGAGATGGGG | 10054 |
rs529320684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34460072 | CTAAATGCATGGAAC[A/G]GGGAGACTTATCTGA | 10054 |
rs529420542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467407 | CAGGAGTTCGACACT[A/G]CAGTGAGCCATGATT | 10054 |
rs529440164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34440593 | AATTGCTAGTCAGTC[A/T]CACACCTAAATAATA | 10054 |
rs529446040 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34447050 | GAGTATTAATTCACA[C/T]GATCACAAGGCCCAA | 10054 |
rs529450307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34439724 | ACTTGGGAGGCCGAG[A/G]TAGGAGGATCAGTTG | 10054 |
rs529509154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34446362 | TTTCTTTCTGCTGGA[A/G]AGAATCCACTTTCGG | 10054 |
rs529576069 | in-del | -/A | 0.132409 | 0.220618 | intron-variant | UBA2 | GRCh38.p7 | 19:34438220 | CACTTAGTTTTGCTC[-/A]AAAAAAAAAAAAAAA | 10054 |
rs529610691 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428273 | AGAGCCTGCCGGTCC[C/G]CGCGGGCTGCAGCAC | 10054 |
rs529625366 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34445591 | TTACAGGTGTGTACC[A/G]TCAGGCCTGGCTAAT | 10054 |
rs529701966 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454717 | GTGTGTTTAAGCTTC[C/T]TGGAAATTGCAACAA | 10054 |
rs529827233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34434272 | GGTACCACCATACCC[A/G]GCTAATTTTTTTATG | 10054 |
rs529893980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447832 | TAGGGAGAGGCTTCA[G/T]AAGAGGCTTTCTAGA | 10054 |
rs529950935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34462824 | TACAAAAATTAGGCC[A/G]GGCGTTGTAGCTGTA | 10054 |
rs530248072 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34429746 | GAGGCTGTGTCAGGA[G/T]GATCGCTTGAGCCTG | 10054 |
rs530356886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436430 | TCAGTCTCCCGAGTA[C/G]CTGGGATTACAGGCG | 10054 |
rs530378535 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470371 | TAAAGCTCTTCCTGC[A/G]TGTGGTGGTGGTGCA | 10054 |
rs530467813 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466110 | GGAGGCTGAGGCGGG[C/T]GGATCACAGGCTCAG | 10054 |
rs530481088 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426775 | AACACTCCCAGCCAT[G/T]TTCAGACATGCTCTG | 10054 |
rs530543504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34433495 | TTTAATATTTATTAG[A/G]CTATTGTGATTTAGA | 10054 |
rs530599446 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34462729 | CTAGCACTTTGAGGG[A/G]CCGAGGCGGGCAGAT | 10054 |
rs530699257 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463344 | ATTCCCAGCGTTTTA[A/G]TGTTTTAGGGTACTA | 10054 |
rs530777065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34461980 | AATGAACATCTGTCT[A/G]CAAAGGTGTGAACTT | 10054 |
rs530789212 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34468592 | TCATTCACTGAGTTT[A/C]CTTTCCTGGAAAGCA | 10054 |
rs530924364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441194 | GGCGAGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 10054 |
rs530970443 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34428975 | GTAACTCCGAAGTAA[C/T]GACGCGGGGCGGAGG | 10054 |
rs530993341 | snp | A/G | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34455631 | TTATTTTGCAGTGTC[A/G]TTGATGCACACTTAC | 10054 |
rs531248842 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBA2 | GRCh38.p7 | 19:34464431 | GGCATAGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 10054 |
rs531249155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34456544 | TTATATTTTTAATTT[C/T]TAAGAACTTTATTTT | 10054 |
rs531262656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435271 | GACATGGTGGCCGGC[A/G]CCTGTAATCCCAGCT | 10054 |
rs531324004 | snp | C/G | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427138 | GGTCTTGCTCTGTCT[C/G]TCAGGCTGGAGTGCA | 10054 |
rs531388362 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454882 | TTTAAAATTTGCTTG[A/G]TCATTTTATAGTCCC | 10054 |
rs531390964 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34463920 | CTTTGGATTTTGGTG[A/T]ACGGGACACAAATCA | 10054 |
rs531394812 | snp | G/T | 0.139903 | 0.224452 | intron-variant | UBA2 | GRCh38.p7 | 19:34444062 | TTTTTTTTTTTTTTT[G/T]TTTTTTGTCTCAGAG | 10054 |
rs531406361 | snp | C/T | 0.000148457 | 0.00861432 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34450313 | ATGGACAAACTATGG[C/T]GGAAAAGGAAACCTC | 10054 |
rs531520827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436496 | TAGAGACGGGGTTTC[A/T]CTATGTTGGTCAGGC | 10054 |
rs531644910 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432850 | GTGAGCCACTGCACC[C/T]GGCCTGTATCTCCGG | 10054 |
rs531683418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430980 | GGGGGCTAGAGGAGC[A/G]TTATGCTGCTGTCCT | 10054 |
rs531849481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34458510 | AGCCTGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 10054 |
rs531863681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466003 | GGGACCCAGAAATCA[C/T]GTAGTTCTGCCCATA | 10054 |
rs532052265 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443015 | ATTAAACAGTTTTTA[G/T]GATAACTTTATTAAT | 10054 |
rs532056290 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470216 | GTGAGCCAAGATTGT[A/G]CTATTGCTACTCCAG | 10054 |
rs532091337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34428830 | TCCCCGGCAGCGCCA[A/G]TGTGTGGCGCTTCGT | 10054 |
rs532111536 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455119 | TATTTCTTCAAAGAG[C/T]ATTTGTGGTTATTAT | 10054 |
rs532182948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34457050 | AGTAATATATCTGGC[C/T]GGGCACGATGGCTCA | 10054 |
rs532189836 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469544 | ATTGTGGTTTAGTAA[A/G]GTTGATACCTGGTTA | 10054 |
rs532281011 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428317 | GTGCCCTGCCTGTGT[C/G]TGCCGGAGGCTGTAG | 10054 |
rs532335121 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34442037 | CCCAGCAGTTTGAGA[A/G]CAGTGTGGGCAACAT | 10054 |
rs532507298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437019 | CAAGAAAGCATATTG[A/G]AAGGCTGAGGGCATC | 10054 |
rs532507414 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34429839 | AGACCCTGTCTCAAA[A/G]AACAAAGAAAAAGAA | 10054 |
rs532534768 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34442718 | TTACACATGTGAGCC[A/C]CCACGCCCAGCCAAA | 10054 |
rs532581245 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467400 | TTGAACCCAGGAGTT[A/C]GACACTGCAGTGAGC | 10054 |
rs532721687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465906 | CCCACCCCTTAAAAC[A/G]TGTGTCTTTTGTTTG | 10054 |
rs532785921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34444030 | AATGTGTGTTTAACA[C/T]GTGTTTTTTTTTTGT | 10054 |
rs532798607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465423 | GCGGGTGGATCACGA[G/T]GTCAGGAGTTCAAGA | 10054 |
rs532901592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430460 | GCGATTCGAAAAACG[C/G]TTTCTCCACTAATGT | 10054 |
rs532966336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34451110 | GGGCTCAAGCCATCC[G/T]CCTCCCTCAGTCTCC | 10054 |
rs532985556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34431112 | CTGTTTGGCAAACCC[C/G]CACTTGTTTCTCTTT | 10054 |
rs533018208 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34450453 | TGTTGCTTGAAAATG[A/C]TATGTCTTCATATAT | 10054 |
rs533027808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34458416 | ATACAAAAAATTAGC[C/T]GGGCGAGGTGGCGGG | 10054 |
rs533090846 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34430822 | AAAGGACTAAAGATT[A/G]AGCCCTCCTTTTTTG | 10054 |
rs533093639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437703 | AGTTGTCTCAGGTGT[C/T]ATGTACTTCTTCCAA | 10054 |
rs533136137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34459914 | TTCTTTTCTAGGAAA[C/T]AATTATCTTTGGTAT | 10054 |
rs533178246 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433536 | CTTAAGAGAAATGAT[C/T]GAGTTTAAAGCATGC | 10054 |
rs533226243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466731 | AGACCCTATCTCTCA[G/T]TTTTTTTTAAATAAA | 10054 |
rs533370196 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34445687 | AAGTGATCTGCCCAC[C/G]TTGGCTTCCCAAAGT | 10054 |
rs533403933 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456188 | GATGTGATCTCGGCT[C/G]ACTGCAACCTCCACC | 10054 |
rs533407651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467364 | GTAGTCTCCGCTACT[A/C]AGGAGGCTGAAGTGG | 10054 |
rs533416690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34453016 | ACAGAGGCTAAATAA[A/G]GAGCCCTTGGAATGG | 10054 |
rs533540119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442918 | TATAGTTGGGTGGGG[G/T]GTTGTACAAAGGATT | 10054 |
rs533551771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442251 | CACAAAAAAGATAAT[C/T]TGGCAAAATTAATAT | 10054 |
rs533568343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446278 | GACCTTAAGGATATA[A/G]TAACAGGTTTGAAAC | 10054 |
rs533867444 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34436623 | GTTTTTAAAACCTCA[A/G]CACGGCTTCATTTGC | 10054 |
rs533966020 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443598 | AGGCGTGCGCTACCA[C/T]GCCTGGCTAATTTTT | 10054 |
rs533985789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34458192 | GGTTGCAGAAGAACG[C/T]GGAGTCTTATATAAT | 10054 |
rs534126588 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34429432 | CGGGTGGCCGACTGA[C/G]TCATTGTTTCTTTCC | 10054 |
rs534258833 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34429764 | TCGCTTGAGCCTGGG[A/G]GGTCGAGGCTGCAGT | 10054 |
rs534388240 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34437909 | AAAATATGAAAATTA[A/G]CTGGGAGTGGTGGGA | 10054 |
rs534398784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34437385 | GAGGCCAAGGCGGGC[A/G]GATCACCTGAGGTAA | 10054 |
rs534405683 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34444059 | GTTTTTTTTTTTTTT[G/T]TTTTTTTTTGTCTCA | 10054 |
rs534450991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34431397 | GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCT | 10054 |
rs534469393 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440429 | TTATTTTTACAGATT[C/G]ATTTCACAAAACTTG | 10054 |
rs534470967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443660 | TTGGTCAGGCTGGTC[C/T]CGAACTCCTGACTTT | 10054 |
rs534480249 | in-del | -/TTTCTT | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34444916 | ATTTCCATGAGTGAC[-/TTTCTT]TTTATTCCCAAAGGT | 10054 |
rs534559653 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34452467 | ATAGAAGTCATAAAA[C/T]CATTTGGAGAAAACA | 10054 |
rs534634334 | snp | C/G | 1.64784e-05 | 0.00287035 | intron-variant | UBA2 | GRCh38.p7 | 19:34431842 | TATTGTAGTAATTCA[C/G]TGTTGTTTATTTTTC | 10054 |
rs534637604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466459 | ACCCAGTTTTATGCT[G/T]CAGCAATAAAAGTTA | 10054 |
rs534642086 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437594 | CAACCTGGGCAACGA[A/G]CGAAATTCCGTCTCA | 10054 |
rs534691587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34439816 | TAGTGAGATCCTGTC[G/T]TAAAATGAAGAAAGA | 10054 |
rs534696866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34433042 | AATGTGTTCTTTATG[C/T]GTTCCCAGGCACTTG | 10054 |
rs534720191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446463 | TGTCCTGTGTCTCGG[A/G]TCTTTTTTTTCTTGG | 10054 |
rs534740737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438431 | TGAACCAGGAGTCGG[C/T]GTCCTGGCACAGCCT | 10054 |
rs534798800 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453293 | GATGCCTCTGAATTT[G/T]AGACCAGGGTGATAT | 10054 |
rs534887946 | in-del | -/TTAA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457883 | TATTTGCCTTGGTTC[-/TTAA]TTATTTTTTTGTTTA | 10054 |
rs534940328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34455804 | GCATGCCACCATGCC[A/G]GCTAATTTTTGTATT | 10054 |
rs534981742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34457511 | CACACTTACCTTCCC[C/G]GTGAAGCCCAAAATC | 10054 |
rs535018971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34468976 | CAATTATAGAAAATA[C/G]AGGTGAGCACAGGTA | 10054 |
rs535109290 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430796 | TTGTGAAGGATAAAG[A/T]TATATCAAGTAAAGG | 10054 |
rs535171046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437367 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGCGG | 10054 |
rs535232955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34460279 | TGATCTGCATCAGTG[G/T]TCAGATGTGGGGATG | 10054 |
rs535316125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34458716 | TTTTAGATTGTATGG[C/T]GTATAAAATTACAGC | 10054 |
rs535350518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466336 | GTGAGACTCCGTCTC[A/G]AAAAAAAGAAAAAGA | 10054 |
rs535423270 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34431155 | TTGGCTTCCTCCTCC[A/C]GGAGTACTTTCCTAA | 10054 |
rs535433581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34445769 | TTCTTGCTCATATCT[G/T]CTATTAGCAGTTTGA | 10054 |
rs535508565 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34452368 | GGATTCTAGTGATGT[A/G]TTCAGGGTTTATAAT | 10054 |