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 |