SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs189197 | snp | A/T | 0.32627 | 0.238082 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894004 | TAACTAAGATCAGAG[A/T]ATGACACTGTCCTTT | 92912 |
rs191394 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897759 | CACATCAGCCCAGGA[A/G]CTTGAGGCTGCAGTC | 92912 |
rs335687 | snp | A/G | 0.0973687 | 0.197999 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899625 | AAATGAGCAAAATGC[A/G]AAGGCTGTAACTTAT | 92912 |
rs335688 | snp | A/G | 0.00666292 | 0.0573329 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899511 | TTTTGTCTGCATGTT[A/G]GAAAGATTTTCTTTA | 92912 |
rs335689 | snp | C/T | 0.012886 | 0.0792272 | utr-variant-3-prime, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899461 | ATACAACAGTCAACA[C/T]ATTTAGCCATCTTCC | 92912 |
rs335690 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899013 | TCCACCTCCCCAAAG[C/T]GCTGGGATTACAGGT | 92912 |
rs335691 | snp | A/G | 0.029116 | 0.117091 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897795 | CAGTCCAAGCTACTG[A/G]GGAGACTGAGGCAGG | 92912 |
rs335692 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897283 | CCACTGCACTCCAGC[C/T]GGGGTGACAGAGCGA | 92912 |
rs335708 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894303 | taggattataggagt[A/G]agccactgtccctgg | 92912 |
rs335709 | snp | A/G | 0.029116 | 0.117091 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893518 | tcttactagtagtac[A/G]cagggtatgttgaaa | 92912 |
rs335710 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892780 | caagtgatcttccca[C/T]ctcagcctcctgagt | 92912 |
rs335711 | snp | A/G | 0.324145 | 0.238752 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892399 | ctgtgttctgtatct[A/G]ataattccaaaacct | 92912 |
rs335712 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891538 | TAATAATAGCACCTA[C/T]TTTTTAAGTTATTAA | 92912 |
rs335713 | snp | A/G | 0.171057 | 0.237209 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890608 | TTCTTGAAAGTAGAC[A/G]CTATTTTAAAAATAA | 92912 |
rs335714 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890255 | ATTCTAATGTTATCA[C/T]GCTAATGTAATCCCT | 92912 |
rs335715 | snp | A/T | 0.324619 | 0.238604 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890065 | CTTTCTCTACCATGT[A/T]ACAGCCATGAGTTTT | 92912 |
rs335716 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889393 | CATTAATAATTGTTA[C/T]AGTGACAATATTTAA | 92912 |
rs335717 | snp | G/T | 0.144632 | 0.226711 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889181 | GGATTAAATTTTTTT[G/T]TGTGTATTCTATTTC | 92912 |
rs963249 | snp | A/G | 0.009685 | 0.0689108 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887582 | TACTTAGCAGAGGGG[A/G]AAAAAAAAAAAAAAA | 92912 |
rs1020416 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864275 | aattactgTGTAAAC[C/T]AGATCTACACCCTAG | 92912 |
rs1039547 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883969 | TTAGGATCACAGGCA[C/T]GTGGGGACCATTCTC | 92912 |
rs1131973 | snp | A/T | 1.66081e-05 | 0.00288163 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75877969 | TTAACAGGGATTTAT[A/T]CAGTGGAACTCATAA | 92912 |
rs1183602 | snp | A/G | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885910 | TCATGATCAGTTTTG[A/G]AAGTGGAATGTTAGG | 92912 |
rs1183603 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885966 | CAAAATAAACACAAG[A/G/T]CTGAAAAATAGTAAA | 92912 |
rs1185088 | snp | G/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886115 | GAAATGACATAACTA[G/T]TGTGTTTTAGttttt | 92912 |
rs1394123 | snp | A/G | 0.029116 | 0.117091 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878862 | AATCTAATCTAGTAA[A/G]GGAGTTCAGAGTTTG | 92912 |
rs1394124 | snp | A/T | 0.029116 | 0.117091 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878817 | GAAAATAGTCACATG[A/T]ATATAATTTTCTCAA | 92912 |
rs1394125 | snp | A/G | 0.379942 | 0.213577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866642 | ACTTACATCTCTTCT[A/G]TTTTCTCCCCCATCT | 92912 |
rs1394126 | snp | A/G | 0.0487975 | 0.148383 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866754 | TCTGGCCCTTCTACA[A/G]GTGGTTTTTTGGGGG | 92912 |
rs1532783 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898565 | GTATATTGTTAACTA[C/T]AGTCACCATGTTGTA | 92912 |
rs1562403 | snp | A/G | 0.170733 | 0.237101 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864468 | ctcagcaatattgac[A/G]tattgggccagacaa | 92912 |
rs1613718 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865825 | TTTTTTTTTAACCTA[A/G]AAAGGGTTTAAAGGG | 92912 |
rs1618530 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848148 | GCAAGAGAGCATATA[G/T]AGGAAAGCTCTTTGG | 92912 |
rs1621882 | snp | A/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855743 | TTGATTCTTAGGTAT[A/T]TAATTTTTGTTGAAA | 92912 |
rs1665763 | snp | A/C | 0 | 0 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842647 | CACACCCCCATGGAG[A/C]TAGGGCTGCCCACTA | 92912 |
rs1665764 | snp | A/C | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872878 | TTAAAATGAAAAACA[A/C]TACAAAAAAGAATAG | 92912 |
rs1665765 | snp | G/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879816 | TCCAtaaataagtgt[G/T]tctcagatttctttt | 92912 |
rs1665770 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865522 | taagtatgtgcccca[A/G]agaaatgctggcaca | 92912 |
rs1665771 | snp | A/G | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865520 | AGTATGTGCCCCAGA[A/G]AAATGCTGGCACAGG | 92912 |
rs1695378 | snp | C/T | 0.324382 | 0.238678 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888205 | GTTTCTTTTTGAAGT[C/T]ATGAAAATGTTCTGA | 92912 |
rs1699269 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848100 | TCTATAGTACACAGA[A/C]ACACAGTAAAAGAAG | 92912 |
rs1699270 | snp | A/C | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848015 | TAGATTCACAGCTCC[A/C]ACATTTTTAAAATTT | 92912 |
rs1699271 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879809 | ataagtgtttctcag[A/T]tttcttttcattttt | 92912 |
rs1699272 | snp | C/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865557 | CATGAGGATCAATTT[C/T]TTCTTTTACTCAAGA | 92912 |
rs1699273 | snp | A/C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865560 | GAGGATCAATTTTTT[A/C/T]TTTTACTCAAGAGTT | 92912 |
rs1699274 | snp | C/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865578 | TTACTCAAGAGTTAT[C/T]TAGGAAAAAAAAAAC | 92912 |
rs1699276 | snp | C/T | 0.031825 | 0.122064 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888334 | TTTTATATGATTCTA[C/T]TTATATGAAATGTCC | 92912 |
rs1699277 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888057 | AAATGTTTGGCTATG[G/T]CAAGAAATAAAGAAG | 92912 |
rs1699278 | snp | C/T | 0.029116 | 0.117091 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887641 | TGTCACTCCCCTGTT[C/T]CTCAACCAGTTATAC | 92912 |
rs1699279 | snp | C/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881809 | CCAAAAAGTGACTTC[C/T]TTAAAAATATAGCAA | 92912 |
rs1799634 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848031 | ACTTCTCACTTCCTC[A/C]TAGATTCACAGCTCC | 92912 |
rs1868020 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883487 | TAGTGAGATCTCGTC[C/T]CTATAAAAAAAAATT | 92912 |
rs1910510 | snp | G/T | 0.13446 | 0.221699 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896767 | TTATAAAAATGAACT[G/T]TGAGGCTTGTTGAGT | 92912 |
rs1910511 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882640 | AACAACAGTTATTAT[A/G]ATCTACTTTCAAATA | 92912 |
rs1964677 | snp | A/C | 0.029116 | 0.117091 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885719 | GATCAACTTTGTAAC[A/C]ACCTGTCAAAAGGAA | 92912 |
rs1968623 | snp | A/G | 0.029116 | 0.117091 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871821 | TTCCTATCAATAATt[A/G]tggggaaaagcaaga | 92912 |
rs1976748 | snp | A/G | 0.499908 | 0.00678851 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868610 | TATTTTAAATAAGCC[A/G]TTGATCTTATGCATA | 92912 |
rs2028949 | snp | A/C | 0.029116 | 0.117091 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858725 | CGGACACAGACCTAG[A/C]CACTCTGGCCTCTGG | 92912 |
rs2028950 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858518 | AGTAAGAGACATTCA[A/G]AAGGACAGGTCTTAG | 92912 |
rs2047866 | snp | A/G | 0.478396 | 0.101662 | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843853 | GGGCCGCGGCCGGGC[A/G]CCTCACCGTGATGTT | 92912 |
rs2047867 | snp | C/T | 0.029116 | 0.117091 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886388 | ctcatgccataatcc[C/T]agcactttgggaggc | 92912 |
rs2121556 | snp | A/C | 0.121828 | 0.214644 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854622 | TTGAAGGAAAAAAAA[A/C]AAACAAACTAGTCTT | 92912 |
rs2134736 | snp | C/T | | | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844124 | GGGCCGCCGCGGACT[C/T]CCCCCTCGGGGCTAG | 92912 |
rs2307792 | in-del | -/TTC | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900574 | AATGTGCTTCTGGAT[-/TTC]TTGTTAAAAGTGCTT | 92912 |
rs2441928 | snp | G/T | 0.170408 | 0.236992 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858828 | TGGAGCTTGGTTTCC[G/T]TTTAAGCATGAAGAT | 92912 |
rs2441929 | snp | A/G | 0.324382 | 0.238678 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880779 | GCTGGGATTACAGGC[A/G]TGATTTAATATGGAT | 92912 |
rs2441930 | snp | A/G | 0.317692 | 0.240661 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881190 | TCTTTTTAAAAAATT[A/G]AATTATATGTCCTTA | 92912 |
rs2441931 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881260 | TTTATCCGTCCCTGT[A/G]GCCCCCTGTGTGCCC | 92912 |
rs2441932 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881439 | AATGGCTGAATTTCT[A/G]TTGGATTTGTGTTTC | 92912 |
rs2455896 | snp | C/G | 0.0739622 | 0.178423 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882838 | CCCAACCTAAGGAGC[C/G]GGAGACTTAGCAGGG | 92912 |
rs2455899 | snp | C/T | 0.323908 | 0.238825 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879466 | ACCCATCTTGTCCCA[C/T]ATAGCTGTAAACCAC | 92912 |
rs2455900 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874388 | GGTGAGGCAGGAGAA[C/T]TGCTTGAACCTGGGA | 92912 |
rs2455901 | snp | C/G | 0.029116 | 0.117091 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863976 | ATATTCAGTGAAAAA[C/G]ACAAGCTGCAGATGT | 92912 |
rs2460798 | snp | A/G | 0.326976 | 0.237854 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883787 | TTACCTATCAACAAC[A/G]TAATGCTTTACAACT | 92912 |
rs2460799 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880563 | agtgagccaagattg[C/T]gccaccacacgccag | 92912 |
rs2460800 | snp | G/T | 0.324382 | 0.238678 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872610 | GTTTGAGGCTGCAGT[G/T]AGCTATGATCATGCT | 92912 |
rs2460801 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872007 | CCTACATGTTTTCCT[C/T]ACAATTCTCACAAAT | 92912 |
rs2460803 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851398 | gtgaaccactatttt[C/T]taaatgaccaatgca | 92912 |
rs2593274 | snp | A/G | 0.0287284 | 0.116357 | | | GRCh38.p7 | 15:75851892 | TTCTTTTTATTTTTG[A/G]GACAGGGCCTTGTTC | 92912 |
rs2593275 | snp | A/G | 0.17138 | 0.237316 | | | GRCh38.p7 | 15:75852640 | TTCTTTAGCCTAAGG[A/G]AAAAGAAACCTAAAA | 92912 |
rs2593276 | snp | C/T | 0.0209421 | 0.100162 | | | GRCh38.p7 | 15:75853267 | ACGAGATCAGGAGTT[C/T]AAGACCAGCCTGGCC | 92912 |
rs2593277 | snp | A/G | 0.32627 | 0.238082 | | | GRCh38.p7 | 15:75853284 | AGACCAGCCTGGCCA[A/G]CATGGTGAAACCCCG | 92912 |
rs2593278 | snp | C/T | 0.325799 | 0.238232 | | | GRCh38.p7 | 15:75855256 | AGCACTTTAGGAAGC[C/T]GAGGCGGGCGGATCA | 92912 |
rs2593279 | snp | A/C | 0.0287284 | 0.116357 | | | GRCh38.p7 | 15:75855272 | GAGGCGGGCGGATCA[A/C]TTGAGGCCAGGAGTT | 92912 |
rs2593280 | snp | A/G | 0.326035 | 0.238157 | | | GRCh38.p7 | 15:75858624 | TGAAATTCGTGGAGA[A/G]TGTACTACCCTGTCT | 92912 |
rs2593281 | snp | A/G | 0.170408 | 0.236992 | | | GRCh38.p7 | 15:75860847 | CTTGGATCCCATGCC[A/G]TCTTTCTTGGCTGAC | 92912 |
rs2593282 | snp | C/G | 0.0232847 | 0.105357 | | | GRCh38.p7 | 15:75863227 | GCTGTCAATATCCCC[C/G]TAACCTCCACCTTTG | 92912 |
rs2593299 | snp | C/G | 0.113334 | 0.209338 | | | GRCh38.p7 | 15:75844766 | ACTGCAGAATATTCT[C/G]TTGGTTATAATAGGC | 92912 |
rs2593300 | snp | C/T | 0.0209421 | 0.100162 | | | GRCh38.p7 | 15:75847193 | TAAATGCTTCATAAA[C/T]ATTTGAGTATATAGC | 92912 |
rs2593301 | snp | C/T | 0.029116 | 0.117091 | | | GRCh38.p7 | 15:75849086 | AAGTGTTAGAATTTT[C/T]ACTCTGCTTTTGTGG | 92912 |
rs2593302 | snp | A/C | 0.170408 | 0.236992 | | | GRCh38.p7 | 15:75849339 | TATCTCTGAACCTTC[A/C]AGAAGTTTGTGCATC | 92912 |
rs2604403 | snp | C/G | 0.170084 | 0.236883 | | | GRCh38.p7 | 15:75861341 | CTGAAACTCAGAATG[C/G]CATGAGGCTTCACCA | 92912 |
rs2604405 | snp | A/G | 0.170084 | 0.236883 | | | GRCh38.p7 | 15:75869788 | ATGTCTTTGGAATGC[A/G]CTCTACTAAATTtgc | 92912 |
rs2604406 | snp | C/G | 0.0678174 | 0.1712 | | | GRCh38.p7 | 15:75867782 | TGAAAGAGCATTTTC[C/G]AAATGCCAATTTCAA | 92912 |
rs2604409 | snp | A/T | 0.0310518 | 0.120672 | | | GRCh38.p7 | 15:75867166 | TCCACCTCTTCCTTT[A/T]AGCTCAGGAGCTGGA | 92912 |
rs2655126 | snp | C/T | 0.170733 | 0.237101 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856169 | GACGGGGTCTCACTC[C/T]GTCACCTAGGCTAGA | 92912 |
rs2655137 | snp | A/C | 0.171057 | 0.237209 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869557 | aggtcctcagacacc[A/C]aatgttggtatcttg | 92912 |
rs2655138 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862642 | TTTTTGTAAAGATGG[C/G]GTCTCAATATGTTGC | 92912 |
rs2675219 | snp | C/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856247 | acacacacacacaca[C/T]gtatatacacatata | 92912 |
rs3040996 | in-del | -/GAAAA | 0.0287284 | 0.116357 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864790 | GCAAAAAATGAAAAA[-/GAAAA]CACTAGATTTAAAAA | 92912 |
rs4886747 | snp | A/G | 0.419616 | 0.183658 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858740 | TCTAGGTCTGTGTCC[A/G]GATTGCTCTGCCTCA | 92912 |
rs4886748 | snp | A/C | 0.495559 | 0.0469148 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882787 | AAGCTGGCTGTCATT[A/C]CCTGTCAGGGCAATT | 92912 |
rs5813808 | in-del | -/T | 0.496999 | 0.0386216 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886126 | ACTATTGTGTTTTAG[-/T]TTTTTTTTTTTGAGA | 92912 |
rs7175758 | snp | A/G | 0.124491 | 0.216211 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886011 | CTTGCTGACACCACC[A/G]GTCTTTTACTAGCCA | 92912 |
rs7496351 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872544 | tttcctttttttttt[C/T]ttttttttttgagat | 92912 |
rs7497829 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856901 | agccgagattgtgcc[A/C]ccgtactctagcctg | 92912 |
rs8024168 | snp | C/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883841 | ATGTATTTATACATA[C/T]ACACACACACACACA | 92912 |
rs8026314 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878424 | tagcaagacttcatc[C/T]ctacaaaaaaaaaaa | 92912 |
rs8027221 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887868 | AAATCAAAATGGCTT[C/G]CTCTTCATAGTCAAC | 92912 |
rs8029590 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884681 | tatttatttattgag[A/G]taggttctcgctttg | 92912 |
rs8030948 | snp | A/G | 0.124491 | 0.216211 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885197 | tgatctcagctcact[A/G]caacctctgccttcc | 92912 |
rs8034430 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876663 | ATTTTTGAAAGCAAG[A/G]TAATCAGCTTTTATT | 92912 |
rs8038729 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880951 | TGGGGATATATCTTA[C/T]GATTGAACTTTCTTG | 92912 |
rs8040550 | snp | A/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856271 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAT | 92912 |
rs8040692 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856302 | atatataATGAATTT[A/C]AGTACAAATCCCAGC | 92912 |
rs8041834 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847856 | CTTCATTTTTTATAT[G/T]ACTTGTAGAGCATAA | 92912 |
rs8182013 | snp | A/G | 0.345482 | 0.231048 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842117 | CTGGAAAAGGAAAAT[A/G]CGGAGCCCCTTTCTG | 92912 |
rs8182037 | snp | C/T | 0.391769 | 0.205917 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842260 | TGCCTCTTGCACTTA[C/T]GATTGCACACACTAT | 92912 |
rs9672219 | snp | C/T | 0.0611083 | 0.163768 | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901468 | CATCTGGGCTTTGCT[C/T]TGCTTCCTTGAGATT | 92912 |
rs10162820 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885129 | AGTGGGGtttttttt[A/T]atttgttttttgaga | 92912 |
rs10524276 | in-del | -/ACACACACACAC | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883854 | TACACACACACACAC[-/ACACACACACAC]GTATATATACGCACA | 92912 |
rs10651661 | in-del | -/AAG | 0.0287284 | 0.116357 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900572 | TTAAGCACTTTTAAC[-/AAG]AAATCCAGAAGCACA | 92912 |
rs11072562 | snp | G/T | 0.499859 | 0.0083854 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899228 | TGCAGTGAGCTGAGT[G/T]TGCGCCATTGCACTC | 92912 |
rs11439832 | snp | A/C | 0.277778 | 0.248452 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878429 | AGACTTCATCTCTAC[A/C]AAAAAAAAAAAATTA | 92912 |
rs11630938 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877750 | GTTTTTCAACTCATT[A/G]AAGAATCTTCTCAGT | 92912 |
rs11633899 | snp | A/G | 0.444444 | 0.157135 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849626 | CAGTTTTATGGTGGG[A/G]ATGGTAGTGGTGATG | 92912 |
rs11634844 | snp | C/G | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862750 | agcctatgaggttaa[C/G]gctgcagtgggctgt | 92912 |
rs11854335 | snp | A/G | 0.00315943 | 0.0396199 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879233 | cttccagtggggtgc[A/G]tatatttgtacaagt | 92912 |
rs11856658 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863629 | attttataAACATCT[A/G]TGATCACCTGGCCAG | 92912 |
rs12324574 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867227 | ACTAAAAACACTCTC[C/T]GTCTTTTCTGTCTGG | 92912 |
rs12324675 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869712 | cctcttaaaggtcct[A/G]cctcttaatagcatc | 92912 |
rs12438642 | snp | G/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872936 | TATGTTAGTATTTCA[G/T]TGGCCTCTTAATATT | 92912 |
rs12593806 | snp | A/G | 0.499933 | 0.00579035 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850491 | AGATCTCCCAGAACT[A/G]GAGGTCTAGCTTCAG | 92912 |
rs12898403 | snp | G/T | 0.322721 | 0.23919 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844689 | ATTGAAGTATTAAGT[G/T]TCTCCATAAAAGTGT | 92912 |
rs12903937 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884859 | ttgccatattgctca[A/G]gctggtcttgaactc | 92912 |
rs12908849 | snp | G/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876523 | CTTCTTGATAAACAG[G/T]GAACTCTTACATGAT | 92912 |
rs12909182 | snp | C/T | 0.305934 | 0.243663 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848519 | TTTCGTTTATCTGAC[C/T]AATTTATAATATAGG | 92912 |
rs12909937 | snp | A/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856273 | TGTGTGTGTGTGTAT[A/G]TATATATATATATAT | 92912 |
rs12910494 | snp | A/C | 0.296364 | 0.245663 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857741 | ATAGTTTTATAATAG[A/C]ATATTCTGTTGTAGG | 92912 |
rs12915152 | snp | A/C | 0.300169 | 0.244914 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887041 | TTTTAAAATCTGTTA[A/C]GTAGTTTCTTAATTG | 92912 |
rs16967559 | snp | A/G | 0.333952 | 0.235483 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866606 | ATCTCTATATCTTCA[A/G]TGTCCCTTAACTGTT | 92912 |
rs16967626 | snp | C/T | 0.207864 | 0.246424 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896407 | TATATTAATTCGAAG[C/T]GAAGATATAGGTTGG | 92912 |
rs17427165 | snp | C/T | 0.299916 | 0.244966 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882869 | CCTGTCCTCGGTGGA[C/T]GCTGAGCTCCAGTAT | 92912 |
rs17427298 | snp | C/T | 0.296364 | 0.245663 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889197 | AAAAAAATTTAATCC[C/T]ATGAACCTTCGCCTG | 92912 |
rs17427548 | snp | A/G | 0.0283406 | 0.115616 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900088 | TGTAAAACTGTATCA[A/G]TTAAGGCTTGTGAGT | 92912 |
rs28403288 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881139 | GCACCCAGGCCAAAA[A/C]CAAAAAACAAAACAC | 92912 |
rs28414676 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860215 | TCTCTCTACCACCAC[C/G]TTTTTGTTAATATTG | 92912 |
rs28431332 | snp | C/T | 0.081446 | 0.184634 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862582 | AGTGCTTTGGGAGGC[C/T]GAGGTGGGAGGATCA | 92912 |
rs28438425 | snp | A/G/T | 1.76905e-05 | 0.00297404 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883472 | TTTTCAGTTAAAAAA[A/G/T]ATTTTTTTTTATAGG | 92912 |
rs28461598 | snp | C/G | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854225 | AAGGAGAATGGTTGT[C/G]TCAAAAGTCCAGCTC | 92912 |
rs28488622 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853290 | GCCTGGCCAGCATGG[G/T]GAAACCCCGTCTCTA | 92912 |
rs28517446 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860622 | AGGATATTTCCTTTC[C/T]TGGTGCAGCTTTTTG | 92912 |
rs28525382 | snp | C/T | 0.499997 | 0.00119808 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884896 | TGAAGCCATCTTACC[C/T]GCCTCAGCCTTGCAA | 92912 |
rs28526567 | snp | A/T | 0.151334 | 0.229706 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845716 | GCTAGGAGTACAGGG[A/T]TACCAAATGTTTTGC | 92912 |
rs28544014 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856269 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAT | 92912 |
rs28548962 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851176 | TCACTGTGTTGCCCA[A/G]GCTGGAGTGCAGTGG | 92912 |
rs28550045 | snp | A/G | 0.499913 | 0.00658888 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848145 | ACTGCAAGAGAGCAT[A/G]TAGAGGAAAGCTCTT | 92912 |
rs28606602 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877868 | AAGAGCAAAATTTCT[A/G]GCTTTCGTTGGCTAT | 92912 |
rs28607641 | snp | A/T | 0.496483 | 0.0417852 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899303 | ATAATATATATATAT[A/T]TTTTTTACGGTAGAT | 92912 |
rs28631664 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843975 | CAGGCCCGCCCCTTT[C/T]CCCCGCGACTTGCCC | 92912 |
rs28663102 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877797 | CTGTTAAGGGCATAA[A/G]ATACTCAGCTGCAGT | 92912 |
rs28671468 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877875 | AAATTTCTAGCTTTC[C/G]TTGGCTATTTAGTGT | 92912 |
rs28685283 | snp | A/T | 0.00489924 | 0.0492506 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883473 | TTTCAGTTAAAAAAA[A/T]TTTTTTTTTATAGGG | 92912 |
rs28696039 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879411 | AATAGAAAACCCAAG[A/T]GTTCATTCCAATAAA | 92912 |
rs28707038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866353 | GGCTACTTTTTAAAA[A/T]TTTTTTGTAGAGATG | 92912 |
rs28720874 | snp | A/G | 0.377385 | 0.215112 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841292 | TTGTATATATTTCTG[A/G]GATACAACTAGTAAA | 92912 |
rs28735570 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879413 | TAGAAAACCCAAGTG[A/T]TCATTCCAATAAAAT | 92912 |
rs33923600 | in-del | -/A/AA/AAA/AT | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876083 | AAAAAAAAAAAAAAA[-/A/AA/AAA/AT]TGTTGAGTGGTGATC | 92912 |
rs34084773 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845177 | ACTTGGGGGAGGTGC[-/T]GCTTCAGGGAAGGCT | 92912 |
rs34089203 | in-del | -/T | 0.170084 | 0.236883 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884706 | CTTTGTTGCTCAGGC[-/T]TGGAGTGCAGTGGTG | 92912 |
rs34101559 | in-del | -/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872554 | TTTTTTTTTTTTTTT[-/T]GAGATAGAGTCTTGC | 92912 |
rs34148087 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864608 | TAACTGTAGATTCTA[-/A]AAAAAAAAAAAAAAA | 92912 |
rs34159094 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859198 | CATGGAAATTTACAG[-/G]TTATTCTTTGCAGTT | 92912 |
rs34177262 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848060 | TTTAGCTTTTATTTA[-/T]GTAGTTAGGAGCTTA | 92912 |
rs34201618 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856314 | TTCAGTACAAATCCC[-/C]AGCAGATTTATTTTT | 92912 |
rs34224049 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860267 | GCTTCTTTCATAGTT[A/T]GTCTTTGGTTATTCA | 92912 |
rs34291503 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877712 | TGCATAATCTTTTTT[-/T]CAGTCAGACTAAACG | 92912 |
rs34292081 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899125 | AAAAAAAAAAAAAAA[-/A]ATTAGTGGGGCATAG | 92912 |
rs34302954 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856294 | ATATATATATATATA[-/A]TGAATTTCAGTACAA | 92912 |
rs34352512 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856292 | ATATATATATATATA[-/T]AATGAATTTCAGTAC | 92912 |
rs34445615 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848904 | TGGAACCTAGGAAAC[-/C]ACCCAGTGGGTTTCT | 92912 |
rs34455718 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849953 | AGAAATAGTAGGCAA[-/A]CTTATCTTTTCAAGA | 92912 |
rs34535776 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848951 | AGATCCTCATCAGCA[A/C]CTTTTTCTGTGCCTC | 92912 |
rs34660479 | in-del | -/A | 0.171148 | 0.237239 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853439 | TGTGCCATGCACTCC[-/A]GCCTGGGCCACAGAG | 92912 |
rs34671622 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867639 | ATTACTTCCCCTTTT[-/T]GAGGTGATGGGGGCT | 92912 |
rs34701345 | snp | C/T | 0.029116 | 0.117091 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875144 | AGTTACTGAACACTT[C/T]TGCATGATGGATACT | 92912 |
rs34855937 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853355 | TGTGCTTGTTATCCC[-/C]AGCTACTCGGGAGGC | 92912 |
rs34977586 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846598 | ATTTGCTTAGAAGGG[-/G]AAAGATCAAGGGAAA | 92912 |
rs35047097 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883725 | TTTTAAGAAGTTTCC[-/C]AGGTGAAGTTGATGC | 92912 |
rs35060618 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893467 | GATAAAACCACAGGG[-/G]AGAAGTTGACAAGTC | 92912 |
rs35076048 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858020 | AAGGCATGTCCCTGT[-/G]CCTCTGGGAACTGAT | 92912 |
rs35134873 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867169 | GCTCCTGAGCTAAAA[-/A]GGAAGAGGTGGAGTC | 92912 |
rs35176335 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855427 | ATCTGGGAGACAGAG[-/G]TTGTGGTGAGCCGAG | 92912 |
rs35201316 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848901 | CTTGGAACCTAGGAA[-/G]ACCACCCAGTGGGTT | 92912 |
rs35380249 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867471 | CTAAGGGTATTCTCC[-/C]TTGTATTTGTTTTTC | 92912 |
rs35429355 | in-del | -/AT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853506 | TATATATATATATAT[-/AT]GTATGTATGTATGTA | 92912 |
rs35518459 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855561 | AATAATCATCATTAT[-/G]TTTCAGCTGACATGA | 92912 |
rs35540616 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872359 | CGTATAAACTACTCC[-/C]TTTAGAGATTTTGGC | 92912 |
rs35542322 | in-del | -/A | 0.330249 | 0.23677 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877480 | GCATTGTTTATATAG[-/A]AAAAAAAAAACAGAT | 92912 |
rs35571341 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848065 | CTTTTATTTAGTAGT[-/G]TAGGAGCTTAAGTAA | 92912 |
rs35656041 | snp | C/T | 0.297382 | 0.245469 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873245 | ATTTTAAATAAAATA[C/T]AGGATATAAAAGGTG | 92912 |
rs35681363 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885412 | GAGCTACCGCACCCC[-/C]ACCTAGTGGTTTGTT | 92912 |
rs35702707 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857658 | CTGTTGATTGTTCCC[-/C]TTGTTGAAACATTCC | 92912 |
rs35753191 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858144 | TCTCTTCTCATTCTG[G/T]GCTTTCTCTGAGTAA | 92912 |
rs35757170 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850789 | CTCTTGAAAATATAT[-/G]TCAGCACTTAAGGGC | 92912 |
rs35784581 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855491 | GTGATACTCCATCTC[-/A]AAAAAAAAAAAAAAT | 92912 |
rs35840590 | in-del | -/A | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872325 | GGGGAAAAAAAAAAA[-/A]GCCGAGATGCGTATA | 92912 |
rs35989972 | in-del | -/A | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857758 | CAAAAAAAAAAAAAA[-/A]TGCAGCCATTTTTTC | 92912 |
rs36056150 | in-del | -/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859217 | TCTTTGCAGTTTTCC[-/C]TAGTGAATTATTGTT | 92912 |
rs36068593 | in-del | -/T | 0.128261 | 0.219371 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875295 | AGCTAGGAAACTTGA[-/T]TTTTTCCCCCCTTCA | 92912 |
rs55982839 | in-del | -/GA | 0.324382 | 0.238678 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886002 | AACCTTTCTCTTGCT[-/GA]CACCACCAGTCTTTT | 92912 |
rs56009854 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882324 | CATTTTAACAGTCAT[C/T]CTCAACCTTTTTTTC | 92912 |
rs56139080 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860301 | ACCTTCACCTAGCAA[C/T]GTCATCTCCTTAAGT | 92912 |
rs56167836 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858728 | GAGGCCAGAGTGTCT[A/G]GGTCTGTGTCCGGAT | 92912 |
rs56297210 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860453 | ATTACCTATTTATTT[A/T]TTTTTTACTATAATA | 92912 |
rs56309552 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881637 | GCAGGTATGACTCAG[A/G]AAGATTTGCAGGAAA | 92912 |
rs56670053 | snp | C/T | 0.0418186 | 0.138422 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899543 | CTTTGAGTGCCCCTA[C/T]TACAGCAGTACCGAA | 92912 |
rs57090077 | snp | C/G | 0.403684 | 0.197183 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842344 | TTTTTTGAGCACCTA[C/G]AATGTGCCAGGAATT | 92912 |
rs57429900 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889597 | AAGCAAGGGAAAGGC[A/G]TGGGCAGAGCCCCGG | 92912 |
rs57600889 | in-del | -/GAC | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874512 | TGGTCTTGAACTCCC[-/GAC]TTCAAGTGATCCACC | 92912 |
rs57626278 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884887 | CTCCTGGGCTGAAGC[C/T]ATCTTACCCGCCTCA | 92912 |
rs57813276 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856975 | TTTTAAGAGTTAAGG[C/T]TGAGGCTTGGCACAG | 92912 |
rs57849079 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867981 | GTCTAAAGAGATGCA[A/G]ATTTAAAGGAAATAC | 92912 |
rs57924900 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859143 | TTTACCTTGCTTACT[-/T]GTTGAAAGCAAATAT | 92912 |
rs57968453 | snp | C/T | 0.0471178 | 0.146078 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879212 | ATAGTTACAGGACCC[C/T]ATATACTTCCAGTGG | 92912 |
rs58030547 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896235 | GGAAGGGGGATGAAC[A/G]GGAGGAAACTGGGTG | 92912 |
rs58733746 | in-del | -/G | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865804 | GAATAATATCTGGTT[-/G]TTTTTTTTTTTTTTA | 92912 |
rs59143042 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888310 | TATCTCTGTAGATTT[A/G]CCTATCTTGGACATT | 92912 |
rs59289858 | in-del | -/AAA | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877183 | AAAAAAAAAAAAAAA[-/AAA]GGGTTATGACCGATT | 92912 |
rs60088262 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887825 | GGGAGTGGAAGGAGG[A/G]ATGAAATGTGAAAGC | 92912 |
rs60490503 | in-del | -/TA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856270 | GTGTGTGTGTGTGTG[-/TA]TATATATATATATAT | 92912 |
rs60496608 | snp | A/C | 0.0663309 | 0.169604 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842203 | CTTCTAAGCTGGGAG[A/C]ACTGTGCAACTACAT | 92912 |
rs60846313 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851853 | TTCAGATGTAGTAAA[A/G]TTTTCACTGCTTCAT | 92912 |
rs60882949 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875997 | CTTGAGCAGGGAGGC[A/G]GAGGTTGCAGTGAAC | 92912 |
rs62027568 | snp | A/G | 0.125874 | 0.217008 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895288 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 92912 |
rs62028927 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843609 | GCGGCTCCGGGCCCG[A/G]CTCCCCTTCCGCGCC | 92912 |
rs62028928 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, stop-gained, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843790 | CAGTTCCTGGTGCCG[C/T]AGCAGGGCAGCCCGC | 92912 |
rs62028929 | snp | A/C/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864626 | AAAAAAAAAAAAAAG[A/C/G]ATCGCTTCATGTATA | 92912 |
rs62028930 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866393 | CATGTTGCCCAAGCT[A/G]GTCTCAAACTTCTGG | 92912 |
rs62028931 | snp | A/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867890 | GAATATAACAATTTA[A/G]GGAAATGAAAAAAGG | 92912 |
rs62028932 | snp | A/G | 0.297382 | 0.245469 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872850 | GCTTATTTCAGCGTA[A/G]CTGAAATTCTTTCTA | 92912 |
rs62028934 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874304 | TTTTTTTTTTTTTTG[G/T]ATGAAGTTACGCTCT | 92912 |
rs62028935 | snp | A/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878443 | CAAAAAAAAAAAAAT[A/T]AGCCAGGCATGGTGG | 92912 |
rs62028936 | snp | A/T | 0.295599 | 0.245806 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890850 | TGAGTTATATACCAT[A/T]TTGTTAGGCCTTCCC | 92912 |
rs62028937 | snp | A/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891500 | GTTTTTTTTTTTTAA[A/T]TCTTTTTATTAACTC | 92912 |
rs66475371 | in-del | -/A/AA/AAA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876082 | TAGACTCCATCTCCA[-/A/AA/AAA]AAAAAAAAAAAAAAA | 92912 |
rs67339230 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899106 | TCTCTACTAAATACC[-/A]AAAAAAAAAAAAAAA | 92912 |
rs67653527 | in-del | -/AAG/GAA | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900573 | TAAGCACTTTYAASA[-/AAG/GAA]AATCCAGAAGCACAT | 92912 |
rs71140182 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862815 | ATGGAACCCTATCTC[-/A]AAAAAAAAAAAAAAA | 92912 |
rs71403520 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847739 | GCAACTCCATTACTC[C/T]TTTTATGGACTTTTT | 92912 |
rs71403521 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881252 | TTTTTTTTTTTATCC[A/G]TCCCTGTAGCCCCCT | 92912 |
rs71440276 | in-del | -/A | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864607 | GTAACTGTAGATTCT[-/A]AAAAAAAAAAAAAAA | 92912 |
rs71440278 | in-del | -/A/AA/AAA | 0.496348 | 0.0425753 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876065 | CTAGACTCCATCTCC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 92912 |
rs72734531 | snp | C/T | 0.318768 | 0.240356 | missense, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844427 | GCGACCCCTCTCCCC[C/T]GGGCCTGGCTGCGCG | 92912 |
rs72734533 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868391 | TCTTGTAGGGAAGTA[C/T]TTTGTTGTAAAATGT | 92912 |
rs72734535 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874307 | TTTTTTTTTTTGGAT[G/T]AAGTTACGCTCTGTC | 92912 |
rs72734546 | snp | G/T | 0.4444 | 0.15719 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896362 | ATAATATAGTGGATA[G/T]ATGGGTACCACTATG | 92912 |
rs72734547 | snp | A/T | 0.4444 | 0.15719 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896363 | TAATATAGTGGATAG[A/T]TGGGTACCACTATGG | 92912 |
rs73449224 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844877 | GGGTACTCAAGTGCC[C/T]GCAGGGTGGCTGGCG | 92912 |
rs73449225 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850195 | TATGGAAAACAAAAC[C/T]TTCTTATTGTAAGAC | 92912 |
rs73449228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859821 | TAGTCATAACATTAT[C/T]GATGTCTTCTAAGGG | 92912 |
rs73449257 | snp | C/G | 0.0119091 | 0.0762411 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900059 | AGTTGTATTGTACTT[C/G]TTAGGCAAAGCAGTG | 92912 |
rs74024005 | snp | A/C | 0.137187 | 0.223099 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849950 | AAGAGAAATAGTAGG[A/C]AAACTTATCTTTTCA | 92912 |
rs74024006 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862237 | GTTCATTGAGGACCA[A/G]CTCCCAAGATGAGCC | 92912 |
rs74024007 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864262 | TTTTTCCTAAGATCT[A/G]GGGTGTAGATCTAGT | 92912 |
rs74024008 | snp | A/G | 0.021333 | 0.101051 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864755 | ATTAGTCTTGTGAAA[A/G]AATCCTCTTTTAGTT | 92912 |
rs74024009 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867798 | GAAAATGCTCTTTCA[A/G]TCGTTGATGCAACCA | 92912 |
rs74024011 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870440 | TAGAATGAGAGTTTA[A/G]TGTTTTTATGCAGTT | 92912 |
rs74024014 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887323 | TGAAGTAGGTGAGAT[C/T]CCAGCTGGGCAGTGA | 92912 |
rs74024015 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891069 | TTTTATATTACTTTA[C/T]AAGCTTTCTTCCTGT | 92912 |
rs74024016 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897703 | GAGTTCTTGTTGTTA[C/T]AACTGGAGTGCAGTG | 92912 |
rs74024017 | snp | C/T | 0.0558544 | 0.157504 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900858 | ATCAGTAAAGTTCCT[C/T]AAGCCTAAGGCTAAA | 92912 |
rs74247799 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876643 | GATTTTTATGATTCC[A/C]CCCCATTTTTGAAAG | 92912 |
rs74331719 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872678 | AGGACCTGAGATAAA[A/G]TTCTTTTTCTAACTT | 92912 |
rs74343680 | snp | G/T | 0.0532157 | 0.154195 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891247 | TCTGTTATATTTGCT[G/T]TAGATAAACATTATA | 92912 |
rs74404862 | snp | C/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862554 | GGGTGTGGTGGCTCA[C/G]ACGTATAATCTGAGT | 92912 |
rs74515368 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874702 | ATGGCTAGACAGTAC[A/G]TACCTTTTGGATGAT | 92912 |
rs74518358 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866615 | TCTTCAATGTCCCTT[A/G]ACTGTTCTCTTACTT | 92912 |
rs74630790 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875307 | TTGATTTTTCCCCCC[C/T]TCAAAGTATAGTGCA | 92912 |
rs74688203 | snp | A/G | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862839 | AAAAAAAAAAAAAAA[A/G]GGACTGAAAGACTGA | 92912 |
rs74822813 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884976 | TTCAAAATTATTTTA[C/T]TATTTTTTGTCCTTT | 92912 |
rs74927538 | snp | G/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866191 | TTACTTTTTTTTTTT[G/T]AAACAGGGTCTTGCT | 92912 |
rs75083913 | snp | A/G | 0.021333 | 0.101051 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855165 | GTTTAAATAGTTGAG[A/G]TCATGGTCTATATAG | 92912 |
rs75130463 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874710 | ACAGTACATACCTTT[C/T]GGATGATTGCTATCA | 92912 |
rs75175361 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898589 | TGTTGTACAATAGCT[C/G]AAGATGGATTCTAGT | 92912 |
rs75187979 | snp | G/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865803 | TGAATAATATCTGGT[G/T]GTTTTTTTTTTTTTT | 92912 |
rs75192522 | snp | A/T | | | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875295 | GAGCTAGGAAACTTG[A/T]TTTTTCCCCCCTTCA | 92912 |
rs75281825 | snp | C/T | 0.0123036 | 0.0774623 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900756 | CAGTAAATAGATTTT[C/T]TGGTATTCTTGTTCA | 92912 |
rs75405411 | in-del | -/TA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883840 | ATGTATTTATACATA[-/TA]CACACACACACACAC | 92912 |
rs75449835 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888124 | ATGATAAAACGCTTC[A/G]AAGTGTACAATTTGG | 92912 |
rs75535146 | snp | A/T | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860265 | TTGCTTCTTTCATAG[A/T]TTGTCTTTGGTTATT | 92912 |
rs75541841 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884382 | ACTTTCTCCAGAAGA[A/G]CTTTGTTCCTACAGT | 92912 |
rs75620899 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870593 | CAAGGGGCCGCAACA[A/T]GGAGGGAAACCTAGA | 92912 |
rs75634133 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879855 | TGAGCAGTAAAACTG[C/T]CCAAAGAGGAAAACT | 92912 |
rs75639965 | snp | G/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880500 | TTTTTTTTTTTTTTT[G/T]AGACAGAATCTTGCT | 92912 |
rs75640399 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882014 | GAGGGTTGATGTTAT[C/T]TTGTCTTCAGCTATT | 92912 |
rs75808918 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861773 | TAATGGCATAAAACA[A/G]CAAATTTGCCTATCT | 92912 |
rs75889317 | snp | A/C | 0.030278 | 0.119257 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875123 | GTTATAGTCAAAACA[A/C]CTATAAGTTACTGAA | 92912 |
rs76030018 | snp | A/G | 0.000149575 | 0.00864668 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854459 | CATCAGTTCTGGAAC[A/G]TCTAGAAGATACTAA | 92912 |
rs76078375 | snp | A/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891497 | CAAGTTTTTTTTTTT[A/T]AAATCTTTTTATTAA | 92912 |
rs76157525 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846006 | GACAGACTATCAGGA[A/G]ATAATTATCATGGCA | 92912 |
rs76186594 | snp | C/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877332 | GCCAAACTTGTTTCT[C/G]AGTTGTTAGAATTGT | 92912 |
rs76187379 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887493 | GGAGGGTAGGACTCA[C/T]GTAGAAGAGTTTTAG | 92912 |
rs76324710 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883876 | CACACGTATATATAC[A/G]CACATACTTTTTACC | 92912 |
rs76363124 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844968 | AGGTGTGTTAATTTC[-/A]AAAAAAAAAAGACAA | 92912 |
rs76457696 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858113 | CCTCTGATCTCTTCT[C/T]CCTTGGCCTACTTCT | 92912 |
rs76512498 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851764 | ACAAGGGTTTTTTCT[A/C]AGGCAGTCTGTAGGA | 92912 |
rs76562945 | snp | A/C | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877159 | AGAGTGAGACTCTGT[A/C]AAAAAAAAAAAAAAA | 92912 |
rs76669428 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845708 | CATTTAGTGCTAGGA[A/G]TACAGGGATACCAAA | 92912 |
rs76806081 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879549 | AATTCCCTTTATATA[C/T]AGTTCAAAAATAGGT | 92912 |
rs76879731 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841716 | TGGGAAGATGGATCA[G/T]AGCTTTTATTAGATT | 92912 |
rs76984720 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848977 | GCCTCAGTTTGCTTA[A/C]AATGATGTTCTCAGT | 92912 |
rs77078223 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887475 | GTTTGAGCTATAACA[C/G]AAGGAGGGTAGGACT | 92912 |
rs77106765 | snp | A/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862841 | AAAAAAAAAAAAAAG[A/G]ACTGAAAGACTGATT | 92912 |
rs77126058 | snp | A/C | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895186 | GCGAGACTCCGTCTC[A/C]AAAAAAAAAATTTTG | 92912 |
rs77130738 | snp | C/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842305 | GGATGTATTCCTTTG[C/G]ACTGCTATCCAGACC | 92912 |
rs77139265 | snp | A/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880485 | AAAAAATGTTAATGA[A/T]TTTTTTTTTTTTTTG | 92912 |
rs77360543 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868246 | TAAAGATGCATGTAT[A/G]AACAGTGTCCTGGCG | 92912 |
rs77437881 | snp | G/T | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870438 | GTTAGAATGAGAGTT[G/T]AATGTTTTTATGCAG | 92912 |
rs77501754 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845026 | ATTGAATGAATACGT[C/T]TGAGTGTTCTGGGCA | 92912 |
rs77517206 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898726 | CAAGTTCCTTGTATT[C/G]TAAATCGCCAGGATT | 92912 |
rs77783668 | snp | G/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880499 | ATTTTTTTTTTTTTT[G/T]GAGACAGAATCTTGC | 92912 |
rs77788798 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875301 | GGAAACTTGATTTTT[C/T]CCCCCTTCAAAGTAT | 92912 |
rs77972002 | snp | A/G | 0.0528689 | 0.153751 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872012 | TGAGAATTGTGAGGA[A/G]AACATGTAGGATGGA | 92912 |
rs77996977 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851751 | ATGACTTAGTCACAC[A/G]AGGGTTTTTTCTCAG | 92912 |
rs78017991 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884131 | CTTACAGAAGGTGGG[A/G]AAAAGATCACAATTT | 92912 |
rs78019974 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874076 | CATCTGCTCTTCATA[C/T]CCTGGAACCACCTGC | 92912 |
rs78045447 | snp | A/C | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872161 | GAGGCCGGGGAGGTG[A/C]AGGCTGCAGTGAGCC | 92912 |
rs78061826 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856904 | CGAGATTGTGCCACC[C/G]TACTCTAGCCTGGGC | 92912 |
rs78140696 | snp | A/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899128 | AAAAAAAAAAAAAAT[A/T]AGTGGGGCATAGTGG | 92912 |
rs78172205 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858776 | ATTATGCACTTAGCA[C/T]GCAATAGAGTGTATT | 92912 |
rs78226459 | snp | C/G | 0.0532157 | 0.154195 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874056 | TAGCCACTTTTTACC[C/G]TGTTCATCTGCTCTT | 92912 |
rs78430278 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895525 | ATGTTGAAAAAGACT[A/G]CCCTGTAGAAAAATA | 92912 |
rs78489797 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848959 | ATCAGCACCTTTTTC[G/T]GTGCCTCAGTTTGCT | 92912 |
rs78546011 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892832 | ACTGAGGCATGTTTG[C/T]GCACTCCAGCCTTGG | 92912 |
rs78547853 | snp | A/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857770 | GGCAAAAAAAAAAAA[A/T]ATGCAGCCATTTTTT | 92912 |
rs78631473 | snp | G/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874302 | TTTTTTTTTTTTTTT[G/T]GGATGAAGTTACGCT | 92912 |
rs78760360 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893424 | ATTTTATGTACCTAT[C/T]AGAATAGCCTCAAAA | 92912 |
rs78790719 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860206 | AATTGCCCTTCTCTC[C/T]ACCACCACCTTTTTG | 92912 |
rs78890153 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863252 | CCTTTGTTGGCTTTG[C/T]TCCATTAATTAACTA | 92912 |
rs78913322 | snp | A/G | 0.106633 | 0.204807 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866463 | CAGGCATGAGCCACC[A/G]TGTCCGGCCTTCAGT | 92912 |
rs79007656 | snp | A/T | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848673 | TTGATTTTTTTTTTT[A/T]AATTTGGTTAAACAT | 92912 |
rs79018364 | snp | A/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886879 | AATTTTTTTTTTTTT[A/T]AATCAGAACATTTTA | 92912 |
rs79063526 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898700 | ATGACGTTATGGCTC[C/T]GATAACAGTCCAAGT | 92912 |
rs79090501 | snp | A/C | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876068 | AGACTCCATCTCCAA[A/C]AAAAAAAAAAAAAAA | 92912 |
rs79150906 | snp | A/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864624 | AAAAAAAAAAAAAAA[A/G]GGATCGCTTCATGTA | 92912 |
rs79241469 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883606 | CTGTGCCTGGCCTGC[A/G/T]TTTTTTTTTTTTCTT | 92912 |
rs79268648 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860610 | AATATTTAAGATAGG[A/G]TATTTCCTTTCTTGG | 92912 |
rs79293903 | snp | G/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865804 | GAATAATATCTGGTT[G/T]TTTTTTTTTTTTTTA | 92912 |
rs79361279 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889670 | TAATCAGTGGTCTTA[A/G]CTTTTGTGTTTTCAA | 92912 |
rs79368585 | snp | A/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899126 | AAAAAAAAAAAAAAA[A/T]TTAGTGGGGCATAGT | 92912 |
rs79646556 | snp | C/T | 0.0252325 | 0.109451 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842544 | AACAAAAACTTAGCA[C/T]AGGACGATGTGACAC | 92912 |
rs80020783 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851753 | GACTTAGTCACACAA[A/G]GGTTTTTTCTCAGGC | 92912 |
rs80024008 | snp | A/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875908 | CTACCAAAAAAAAAA[A/T]TACAAAATTTAGCTG | 92912 |
rs80051756 | snp | C/G | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859164 | AAGCAAATATGCTTA[C/G]AAAACAATCTGGACT | 92912 |
rs80150588 | snp | A/C | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857759 | ATTCTGTTGTAGGCA[A/C]AAAAAAAAAAAATGC | 92912 |
rs111280054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882531 | TAAAGATCTAAATAA[C/T]AGGAGGTTAAATGAA | 92912 |
rs111282209 | snp | G/T | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886911 | AATGTGATTATAAAA[G/T]TGGCCAGTATAGCTT | 92912 |
rs111305851 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859785 | AACAAACTTTTTCAT[G/T]TCCTACTGGATTGAT | 92912 |
rs111487358 | in-del | -/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881235 | TTAAGAAATAGAACC[-/T]TTTTTTTTTTTTATC | 92912 |
rs111491069 | snp | C/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888135 | CTTCGAAGTGTACAA[C/T]TTGGTGGTTGTTAGT | 92912 |
rs111527432 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857927 | TTTCCTGGTGGGTAC[A/G]GGAAACTGTCAATAG | 92912 |
rs111546883 | snp | A/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898206 | CACAGATTTCTTCTT[A/G]TCTTTGTTTTTATTT | 92912 |
rs111651071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892297 | GATTAAAAGAATTCA[C/T]TCAAATCATAGCATT | 92912 |
rs111736706 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873843 | TTGGACTATAGGCAC[A/G]TGCCACCATGCCAGG | 92912 |
rs111791675 | in-del | -/T | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859447 | AATATGACTGGAATA[-/T]ATAATTTTGTAATCC | 92912 |
rs111819674 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849912 | GTTTAAAAACTGATA[C/T]ACCATAGGTCATATT | 92912 |
rs111934078 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894675 | AGGAAGGGCTAGACC[A/C]CCAGTACAGTAAAGT | 92912 |
rs111955388 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845805 | CCATCGAGAACCATA[C/T]TGAAGGCTGGTAAGA | 92912 |
rs111958942 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886375 | TCCACCCACCTGGGC[C/G]TCCCAAAGTGCTAGG | 92912 |
rs112001679 | snp | G/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887482 | CTATAACACAAGGAG[G/T]GTAGGACTCATGTAG | 92912 |
rs112005551 | snp | A/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877668 | GAAATGTGTGTTCAT[A/G]GAAGAAAAGTCTTAA | 92912 |
rs112012718 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857822 | TCTAAGATATATTAA[A/G]TGAAAAAGCAAGGCA | 92912 |
rs112125534 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859544 | TGGTAGCCTCATTAA[G/T]GCATTAATGTTCTCT | 92912 |
rs112176632 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879307 | ATGGTTCAGGAATCT[C/G]GTAGACATATTCTCC | 92912 |
rs112177568 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885898 | TGTCATAAAACCTCA[C/T]GATCAGTTTTGGAAG | 92912 |
rs112205665 | in-del | -/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880485 | AAAAAATGTTAATGA[-/T]TTTTTTTTTTTTTTG | 92912 |
rs112228300 | snp | A/G | 0.030665 | 0.119967 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850611 | GTCAAGAGAGGGAGG[A/G]GGAAAGATGGGAGGG | 92912 |
rs112278497 | in-del | -/GA | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891299 | ACTTATTTGTAAACA[-/GA]TGTTTACAGTTGTAA | 92912 |
rs112331078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888782 | TTTGTGTAGTTATTA[C/T]GTACTTGTACAAATG | 92912 |
rs112382016 | snp | A/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887691 | GTAAATCTGGTGACA[A/G]CAGAAGAGAATATGA | 92912 |
rs112424966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858573 | TCCTCCCATCCCTCA[A/G]ATGCTTTTTTGGTGT | 92912 |
rs112437635 | snp | A/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865322 | TTTGTTGTGCTTAAC[A/G]TTGTGTGTGAAATTT | 92912 |
rs112446693 | snp | A/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890403 | AGGAATAATTCTCGA[A/G]AATTTTGTATGACTC | 92912 |
rs112689413 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855317 | CCAACATGGTGAAAC[C/T]CTGTCTCTGCTAAAC | 92912 |
rs112714715 | in-del | -/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874287 | TTTGACTTAACATCC[-/T]TTTTTTTTTTTTTTT | 92912 |
rs112782760 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896430 | TAGGTTGGTTGTACT[G/T]ATGGTGACAAAATTA | 92912 |
rs112888153 | snp | A/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879437 | ATAAAATGGAGAATT[A/G]TGGTGTTTATAAAGT | 92912 |
rs112928171 | in-del | -/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883606 | TGTGCCTGGCCTGCA[-/T]TTTTTTTTTTTTCTT | 92912 |
rs112950460 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851380 | TATGATATTATAACA[C/T]CATGCATTGGTCATT | 92912 |
rs112973023 | in-del | -/C | 0.0966517 | 0.197444 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878427 | AAGACTTCATCTCTA[-/C]ACAAAAAAAAAAAAA | 92912 |
rs113035301 | snp | A/C | 0.0528381 | 0.153711 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865794 | GTATATCCCTGAATA[A/C]TATCTGGTTGTTTTT | 92912 |
rs113078400 | snp | C/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877785 | GGCTGTAATTATCTG[C/T]TAAGGGCATAAGATA | 92912 |
rs113080321 | snp | C/G | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863490 | TCTCTGTCGCCCAGG[C/G]TGGAGTGCAGTGGCG | 92912 |
rs113152931 | snp | G/T | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861587 | TTTTGAAGTGTCCGT[G/T]AATGGGATTTTAGAC | 92912 |
rs113319208 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877134 | CCACCGCACTCCAGC[C/G/T]TGGGCAGCAAGAGTG | 92912 |
rs113367871 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841753 | GGGGTCTGTGAGAAT[C/T]TTAGTCTTCTTAAAG | 92912 |
rs113386683 | in-del | -/AA | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877635 | AAACAACATACGTAG[-/AA]GGATTCCATCTTTGT | 92912 |
rs113500876 | in-del | -/AGA | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877633 | TAAAACAACATACGT[-/AGA]AGGATTCCATCTTTG | 92912 |
rs113618157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860201 | CAAACAATTGCCCTT[C/T]TCTCTACCACCACCT | 92912 |
rs113619061 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862825 | ATCTCAAAAAAAAAA[A/G]AAAAAAAAAAAAAAG | 92912 |
rs113685637 | snp | C/G | 0 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863472 | TTTTTTTTTGACGGA[C/G]TCTCTCTGTCGCCCA | 92912 |
rs113710383 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861441 | ACAACAGTATACTTA[A/G]TGTGGGTCTTTTTTC | 92912 |
rs113714831 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872224 | CGGAGCGAGACTCCA[C/T]CTCAAAAAATAAAAA | 92912 |
rs113719917 | snp | A/G | 0.5 | 0 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886591 | TCAGAATAAATATAT[A/G]AAAACATTTTTATCA | 92912 |
rs113872491 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889623 | CCCGGAGGACAGAAC[A/T]ATTTGTGGTGGACTT | 92912 |
rs113873349 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881304 | TCCTCTTTGAGAGGT[A/G]TCTTTACGGGAATAT | 92912 |
rs114013112 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898583 | TCACCATGTTGTACA[A/G]TAGCTCAAGATGGAT | 92912 |
rs114313706 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881510 | GGGGTTGGAGTATTT[C/G]TTGAGAGGCCTAGGA | 92912 |
rs114316469 | snp | G/T | 0.0236746 | 0.106192 | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901345 | CCTTAGTTCCCCCAG[G/T]GAAAATAATCTGCTC | 92912 |
rs114336664 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859035 | GAAACTGTTCCTGAC[C/T]GAGTTAAGTGAGTTG | 92912 |
rs114379184 | snp | C/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900196 | GAGCCACAGTACAGA[C/G]CTTCAAGTTATTTAA | 92912 |
rs114864846 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898507 | GTTATCATTTTTATG[A/G]TGAGACACTTTACAT | 92912 |
rs114872873 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881583 | CTTAAACTGAATTGC[C/T]AAGTTATTAGTATCG | 92912 |
rs114956710 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882068 | ATTAGTTTTTATTTG[A/C]TTTTGGTGAATGCAG | 92912 |
rs115042779 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898027 | AGGCCAGGTTTTCAT[A/C]ATAATAATTTCTAGC | 92912 |
rs115107637 | snp | C/T | 0.021333 | 0.101051 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842103 | AACTCTAGGTAAGAC[C/T]GGAAAAGGAAAATGC | 92912 |
rs115109921 | snp | C/G | 0.031825 | 0.122064 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868395 | GTAGGGAAGTATTTT[C/G]TTGTAAAATGTTTTT | 92912 |
rs115137809 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868894 | CCAGTCTTCTAATGT[A/G]CTCAGCCTGTGCATA | 92912 |
rs115413686 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889577 | TAGGAAGCAGTAGGA[A/C]TCTCAAGCAAGGGAA | 92912 |
rs115598999 | snp | A/G | 0.00279162 | 0.0372561 | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901271 | GTCACCTTTTCCTCC[A/G]CCTTTTTCCTCTTCC | 92912 |
rs115803910 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866394 | ATGTTGCCCAAGCTG[A/G]TCTCAAACTTCTGGG | 92912 |
rs115833774 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869867 | AGCTCTGAAGCTCTG[C/T]ATTTAAATTCAAACT | 92912 |
rs115868146 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850129 | AACCTTGAACATGAT[A/G]TAGAGTTTGTGCTGA | 92912 |
rs115942477 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858903 | TTGCTCCGTTGTCCA[C/T]TTTGGGAAAGCTTAT | 92912 |
rs115975633 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887350 | GTGAAATGTGAGTGT[C/T]GGGTTTGGTCAGCTG | 92912 |
rs116202155 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893071 | TAGTGGAATCCCAGG[A/T]GGAGATATTAGAATT | 92912 |
rs116208760 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848796 | AAGCATGACTGGAGA[A/G]CCAGAGTGATAAAGC | 92912 |
rs116439762 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887624 | TGGCTATTCATCTTT[C/T]TGTATAACTGGTTGA | 92912 |
rs116439896 | snp | A/T | 0.0103295 | 0.0711199 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842204 | TTCTAAGCTGGGAGC[A/T]CTGTGCAACTACATA | 92912 |
rs116523258 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857357 | AATATTACATAAACA[A/T]GTTCATAAGGTTAAA | 92912 |
rs116538022 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885104 | AAAATGTTCTGTAAG[A/C]ACTAATAGTAGTGGG | 92912 |
rs116596321 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850042 | TGAAAATATTAATAC[A/G]TAGGTTTAAATATTG | 92912 |
rs116686495 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853755 | AGTTGTTGGTGGCAG[A/C]TGTGATCATCCTAAG | 92912 |
rs116757906 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881796 | TGGTAAATCCAACTT[A/G]CTATATTTTTAAGGA | 92912 |
rs117040244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884091 | TCAAATGGTAATTGT[A/G]TTGCTTCTTTTTATG | 92912 |
rs117234254 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868495 | ATCAATAACACATCT[A/G]ACTGTTCAAAATGTA | 92912 |
rs117450315 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845819 | ATTGAAGGCTGGTAA[A/G]AGTCTGCTGCAGATA | 92912 |
rs117625493 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880410 | GAGCCACCACACCTG[A/G]CCTAATAAGTATTTT | 92912 |
rs117799983 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884529 | AATAGTTATTTGGGC[A/G]TGGTGTCCATCTGTA | 92912 |
rs117935159 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855794 | ATCAAGAACATGACA[A/G]TTTTGCTGAGTGGAA | 92912 |
rs117969249 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845374 | AAGCCCACGATACAG[G/T]CTGGAGAAGGGGAGG | 92912 |
rs117981088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881585 | TAAACTGAATTGCCA[A/G]GTTATTAGTATCGGG | 92912 |
rs118061290 | snp | G/T | 0.021333 | 0.101051 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884146 | GAAAAGATCACAATT[G/T]GTTAGGTTAGTTATG | 92912 |
rs118148099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849259 | TCCACCCCACATTTA[C/T]TGAACAGCAAACTAT | 92912 |
rs118186721 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876884 | AGCATTGGTTGGGTG[C/T]GGTGGCTCACACTTA | 92912 |
rs137933994 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881880 | GTAGTACTTTAAGAA[G/T]GGTCTATTTAGATAA | 92912 |
rs138032705 | in-del | -/GTAGAGAAAGT | 0.324619 | 0.238604 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890071 | CATGGCTGTAACATG[-/GTAGAGAAAGT]TTCAGATGTAAAGAA | 92912 |
rs138064160 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847400 | AAAAAGACCAAAACA[G/T]AGTAGATGTTTTACT | 92912 |
rs138078011 | snp | A/C | 0.00231694 | 0.0339574 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843794 | TCCTGGTGCCGCAGC[A/C]GGGCAGCCCGCACTC | 92912 |
rs138139824 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889414 | ATTATTAATGTTAGT[A/G]GTCTACAGTAAAAGT | 92912 |
rs138179496 | in-del | -/TTTG | 0.0611083 | 0.163768 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880109 | TTAATAAGGTTTTTT[-/TTTG]TTTGTTTGTTTGTTT | 92912 |
rs138239549 | in-del | -/GA | 0.0263992 | 0.111815 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842716 | AATAAGGAAAGGGGG[-/GA]GAGAGAGACTATATA | 92912 |
rs138245278 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847956 | GTTAATTAAATTTCT[A/C]TTCATTATTGCCAAA | 92912 |
rs138352693 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860560 | TAATCACTAATTATC[A/G]TTAGGACTTTGTAGA | 92912 |
rs138408567 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857551 | ATAATCTGGATTCTG[C/T]CTTCATCATTGCACT | 92912 |
rs138543320 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869740 | ATCACATTGGCAACA[A/C]CTGCATTTTGGAGGG | 92912 |
rs138702198 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888659 | ATACAGAAGTAGAAT[C/T]GGCCACTTTTAGGTG | 92912 |
rs138764362 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852306 | TTTGTGCTAAAGTGC[C/T]AGCGTTTTTACCCAC | 92912 |
rs138855229 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841862 | AGACTGAATTTGTAG[A/G]CTGTGGGGAGCTACT | 92912 |
rs139027818 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | UBE2Q2 | GRCh38.p7 | 15:75874841 | GCTATTGACCAACTC[C/T]GTGAAATCTGAGTAG | 92912 |
rs139093137 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853658 | AGCTTAAAGCAACAA[A/G]CATTATCTCACCATT | 92912 |
rs139094412 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870417 | AAATACTCTTAAAAC[G/T]GTCAAGTTAGAATGA | 92912 |
rs139160452 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868016 | TAATTCTGCATGGGT[A/G]TGTTTACATGGAATT | 92912 |
rs139274462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862077 | CAGAAGCACAGAAGT[A/G]GAGCTGCCAGGTGTT | 92912 |
rs139408881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849013 | TAATTTGCTGCTTGT[A/G]TTTGAATACTTAAGC | 92912 |
rs139532885 | snp | A/G | 0.000397746 | 0.0140966 | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873454 | CTTAGATCACTATGA[A/G]ATGAAGGAAGAAGAG | 92912 |
rs139580427 | in-del | -/AG | 0.0298908 | 0.118541 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891298 | AACTTATTTGTAAAC[-/AG]ATGTTTACAGTTGTA | 92912 |
rs139588585 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877241 | AATTCTTAGCGTGAG[C/T]AAATCAAAATTAATT | 92912 |
rs139614840 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843533 | TCCAGCAGCGCTCGA[C/T]GAGGCGGAGCCGCGA | 92912 |
rs139627215 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898311 | GCTTAGCTGTGATGA[A/G]AGAGTAATAGAGTCA | 92912 |
rs139758382 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884027 | AAATCTCATGGACCT[A/G]TGGAACTGGCTAATT | 92912 |
rs139773313 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877846 | TAGCTTAGTTGTTCC[A/G]TGTTTTAAGAGCAAA | 92912 |
rs139861338 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864403 | ATTTCTTAGGTAGAG[C/G]GGATGTCACTAAACA | 92912 |
rs139867742 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858848 | AGCATGAAGATTTTT[A/G/T]TTGGATCGTAATTTA | 92912 |
rs140074377 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891238 | TGTTTTTAGTCTGTT[A/G]TATTTGCTGTAGATA | 92912 |
rs140118429 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852727 | GAAGAAGAAAATGCA[A/G]TACTCAATAAGTGGT | 92912 |
rs140154456 | in-del | -/ATT | 0.0134861 | 0.0810011 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887087 | AGTGTTATTGTTCTC[-/ATT]ATTCAAATGAGTAAT | 92912 |
rs140266249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846748 | AAATATTTGAATTCT[A/G]CATGCTAGGACTTGT | 92912 |
rs140503234 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873727 | AAACAGGGTCTTGCT[C/T]TGTCGCCTAGGCTAG | 92912 |
rs140704388 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887140 | CCTACTCAAATAAAT[C/T]TTCTGATTCCTAATA | 92912 |
rs140737853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881196 | TAAAAAATTGAATTA[C/T]ATGTCCTTATGCCTA | 92912 |
rs140845421 | in-del | -/C | 0.0707826 | 0.174302 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859260 | ACACTTAAGAGCCTA[-/C]CTAAATATCAAGTGT | 92912 |
rs140886393 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866255 | ACAGCTCACTGCAGC[C/T]TCTACCTTCCTGGGC | 92912 |
rs141009912 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858127 | TCCCTTGGCCTACTT[A/C]TTCTCTTCTCATTCT | 92912 |
rs141088476 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900852 | CTTTAAATCAGTAAA[A/G]TTCCTTAAGCCTAAG | 92912 |
rs141334593 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880774 | AAAGTGCTGGGATTA[C/T]AGGCGTGATTTAATA | 92912 |
rs141459597 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856369 | ATTTGTTTAAAAGGG[C/T]AAATGATAAAAAAAT | 92912 |
rs141481190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875496 | CGAACTAGACCATCT[A/G]TGTAATATTCTTGTT | 92912 |
rs141546471 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869757 | TGCATTTTGGAGGGA[A/G]CACATTTAAATCATA | 92912 |
rs141568508 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863482 | ACGGAGTCTCTCTGT[C/T]GCCCAGGGTGGAGTG | 92912 |
rs141706132 | snp | C/T | 8.24545e-05 | 0.00642032 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876150 | TCTTAAATCTTAGCT[C/T]AGCAGACCCTGGTAA | 92912 |
rs141805357 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887769 | CCACGCTGTTGTCTT[-/A]AGAGTGAAGTGAGGA | 92912 |
rs141815136 | in-del | -/T | 0.0314385 | 0.121371 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845594 | TAAGTTGGGAGAATG[-/T]TATCTTTCATCCAGG | 92912 |
rs141818608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890636 | GAATGAAAAAGGTAA[A/G]CCAATAAAATGACAT | 92912 |
rs141923901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849507 | TGGAGAAAAATAGAT[A/G]CAGAAAGTTACTTCT | 92912 |
rs142009938 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875909 | TACCAAAAAAAAAAA[A/T]ACAAAATTTAGCTGG | 92912 |
rs142030558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869151 | GGAATATAATTTCCC[A/C]ACTCTGGCTTTACCT | 92912 |
rs142040073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846014 | ATCAGGAGATAATTA[C/T]CATGGCAGCTGCTCA | 92912 |
rs142127873 | in-del | -/TCTT | 0.00557542 | 0.0525036 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858637 | GAGTGTACTACCCTG[-/TCTT]TCTTGTTGCTTGGTA | 92912 |
rs142315305 | in-del | -/AAA | 0.0260105 | 0.111035 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75878625 | AAAAAAAAAAAAAAA[-/AAA]GTTGGGGGGAGGTGG | 92912 |
rs142325116 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871883 | ATTGTTTGAGAAAGA[A/T]AATGTTGAATTCTGT | 92912 |
rs142379146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848531 | GACCAATTTATAATA[C/T]AGGGTCAAATTCCTG | 92912 |
rs142411304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867446 | CAGCATGTCCTTATA[C/G]TTTTAGTTCACTAAG | 92912 |
rs142519754 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858512 | AATTTTCTAAGACCT[A/G]TCCTTCTGAATGTCT | 92912 |
rs142623228 | snp | C/G/T | 9.22751e-05 | 0.00679193 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843800 | TGCCGCAGCAGGGCA[C/G/T]CCCGCACTCGCTGCC | 92912 |
rs142627953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865301 | CTGTATGTATTTTTT[C/T]GTACCTTTGTTGTGC | 92912 |
rs142705825 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847686 | TATTGGGAGCTAGTA[G/T]ATGGCTTTAGTCGTT | 92912 |
rs142780659 | snp | A/G/T | 0.00121854 | 0.0246536 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890948 | CTACTCAATAGAATC[A/G/T]GTCATCATGCAAATA | 92912 |
rs142782160 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883537 | GAATTCCTGGGCTCA[A/G]GTGATCCTCCCACCT | 92912 |
rs142814707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877662 | TTTGTAGAAATGTGT[A/G]TTCATGGAAGAAAAG | 92912 |
rs142839755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848050 | GAAGTGAGAAGTTTA[A/G]CTTTTATTTAGTAGT | 92912 |
rs142886396 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879977 | CGCAGGCTTCTTGGA[C/T]ACTGGCTGGAATATA | 92912 |
rs142903528 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898733 | CTTGTATTCTAAATC[A/G]CCAGGATTTTGTTTG | 92912 |
rs143049101 | in-del | -/GGT | 0.0174175 | 0.0916809 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868436 | TTTGCTTTTTAGTGA[-/GGT]GGTAATCATTTCATA | 92912 |
rs143154486 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867538 | TCTGTCATTTCAGTG[A/G]GGTTTTGAAAAGAGG | 92912 |
rs143235630 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856064 | TAGTGGCACACACTT[C/G]TAGTCCCAACTACTG | 92912 |
rs143297568 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864676 | TATTCACATGTGGCT[A/G]TATGCCGTTTTCACT | 92912 |
rs143307420 | in-del | -/ACACACACACAC | 0.0603597 | 0.1629 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883840 | CATGTATTTATACAT[-/ACACACACACAC]ACACACACACACACG | 92912 |
rs143333229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859378 | TAGGATATCCAAGGT[C/T]ATCTAGATTGCCAGG | 92912 |
rs143547352 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851081 | TATACAGATACCTGG[C/T]TGGAAAAATTGTGAA | 92912 |
rs143656364 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860403 | ACCATCACTAATTTC[A/T]TTCTGGATTTACCTA | 92912 |
rs143722918 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891872 | TATGAAGCTTCCATT[C/G]ACTATGGAGGGAATG | 92912 |
rs143765733 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868461 | ATTTCATAATTCTTA[A/G/T]TTTTGTGAAATGTCT | 92912 |
rs143781093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884234 | CGGGTGACTAATTCT[A/G]TTATGTGACATAATC | 92912 |
rs143835975 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887435 | TCTAGGAAAGAGAAT[A/G]AGATACTCAGAGTAT | 92912 |
rs143934050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861143 | GGATTAAATGAGTTC[A/G]TACAAGTAAACCATT | 92912 |
rs144030980 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882416 | TATGGAATAGAGCCC[A/G]CAGATTTTGATGTAG | 92912 |
rs144077233 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871063 | CTCCGAGAGGGGGAT[A/G]TGTCAGGGTCACAAG | 92912 |
rs144080974 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854618 | TTAAAGACTAGTTTG[-/T]TTTGTTTTTTTTCCT | 92912 |
rs144110983 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890336 | ATGTTATTTTCTCAT[C/G]CTTACTTGTGTGCAT | 92912 |
rs144146450 | snp | A/G | 2.41403e-05 | 0.00347413 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843819 | GCACTCGCTGCCGCC[A/G]CCACTCACGCTCCAC | 92912 |
rs144221015 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896254 | GGAAACTGGGTGTTC[A/T]GGGCACCAAGTAGGA | 92912 |
rs144222813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849725 | GGCCTTAGAATTACT[A/G]TAAAACTAATAGAAT | 92912 |
rs144347215 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844434 | CTCTCCCCCGGGCCT[A/G]GCTGCGCGCTGCTGT | 92912 |
rs144431848 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858401 | AGTGGGACAAAATGA[A/G]ATAATCAAACTAGTC | 92912 |
rs144543960 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871423 | TGTCAGGCTGGGGGA[C/T]GGTCAGGTCTTTCCC | 92912 |
rs144579048 | snp | A/T | 0.00146774 | 0.0270503 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75879125 | TAGTCCTTTGCACAG[A/T]GATCTTCAGATCTTA | 92912 |
rs144581791 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842004 | TGTGTCCCTGTGTTG[C/T]TCTGTATTTTGTCAT | 92912 |
rs144774899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852656 | AAAAGAAACCTAAAA[A/G]CTAAAACAGTAAAAA | 92912 |
rs144800366 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855266 | GAAGCTGAGGCGGGC[A/G]GATCACTTGAGGCCA | 92912 |
rs144919723 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851470 | AAAATACATTCATCA[A/G]TATTGCCATCAATGT | 92912 |
rs144993475 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854755 | CAAACAAGCATTTTG[A/G]GTAGAGACCACTAGC | 92912 |
rs145016432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845693 | TTATTGCTGTGCCGG[C/T]ATTTAGTGCTAGGAG | 92912 |
rs145110766 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881042 | TCAACTGGGTTGTCT[A/T]CCTAAAATATGAGTC | 92912 |
rs145178719 | snp | A/G | 0.00212187 | 0.0325028 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75878012 | ATGACTGGCATGTTA[A/G]ACTGCAGAAGTAAGT | 92912 |
rs145222394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885044 | TATTGTTTCTTAAGA[A/G]TTTACTTACCTGACA | 92912 |
rs145236877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881423 | GACGATCTGGGAGGT[A/G]AATGGCTGAATTTCT | 92912 |
rs145249463 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875503 | GACCATCTGTGTAAT[A/G]TTCTTGTTTGTAGTC | 92912 |
rs145382750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892918 | AGTAGATTAGACACC[A/G]GAAGAGAATTAATTG | 92912 |
rs145429829 | snp | C/T | 7.68049e-05 | 0.0061965 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843757 | ATCGTCAGTTGGAAG[C/T]TGGACGAGCTGCACT | 92912 |
rs145689863 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849219 | TTAAGGTACTATATG[C/T]TAATTCTGTCAATTT | 92912 |
rs145830518 | in-del | -/CGA | 0.0611083 | 0.163768 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874511 | CTGGTCTTGAACTCC[-/CGA]CTTCAAGTGATCCAC | 92912 |
rs145851323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845274 | GAAGGGCATTTTAGA[C/G]TGAGGAAACTCCACC | 92912 |
rs145878680 | snp | C/T | 0.000153988 | 0.00877327 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75883406 | TTGTTCGAGTGGTGT[C/T]ACCTGTTCTCTCAGG | 92912 |
rs145899423 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846260 | TATTATTTTTTGAGA[C/T]GGAGTCTCGCTGTGT | 92912 |
rs145939210 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869339 | CTAAGTTTAAAAAAT[G/T]TTATGTTTGCATAAA | 92912 |
rs145942653 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864395 | CTGTTGGCATTTCTT[A/G]GGTAGAGGGGATGTC | 92912 |
rs146082062 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848172 | TCTTTGGCAATGATA[C/T]TATGTTCTACAAATA | 92912 |
rs146115688 | snp | A/G | 0.0495759 | 0.149433 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844500 | GGTGGTGTTGAGTGT[A/G]TATTCGTGTGGCCCC | 92912 |
rs146122718 | in-del | -/TA | 0.167484 | 0.23599 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853491 | AAAAGAAAAAAAAAT[-/TA]TATATATATATATAT | 92912 |
rs146188147 | in-del | -/T | 0.0479149 | 0.147179 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841833 | AAAAGTTAGGGCTGG[-/T]TTTGAATGATAAGAG | 92912 |
rs146204607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870199 | CAGCCTTCTGAGTAG[C/G]TGGGACTACAGGCGT | 92912 |
rs146237991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865091 | AGTGAATACTTGGGA[A/G]CCAACACCTAGCCAG | 92912 |
rs146276279 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849367 | TCAGTTTTAAAAAAA[-/G]TGATGAAATCCCTGA | 92912 |
rs146305767 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842880 | TCCGGTGAGAAGGTC[C/T]TCACAGGAACCCAGG | 92912 |
rs146312306 | snp | A/T | 0.00474577 | 0.0484805 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844502 | TGGTGTTGAGTGTGT[A/T]TTCGTGTGGCCCCTC | 92912 |
rs146359132 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892143 | CAAGGGTGGGGAGCC[A/T]GATCTCTTGGAGAAT | 92912 |
rs146555735 | snp | A/G | 0.00237701 | 0.0343927 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75897046 | AATTCCATTGTACAG[A/G]TACATGAGAAAAATG | 92912 |
rs146626726 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867495 | GTTTTTCTGCTACTG[C/T]GGCAGACCTACTCTT | 92912 |
rs146713604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897534 | ACCTTAACATTGTAC[G/T]TCAGTCAAAATTTTT | 92912 |
rs146738775 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859653 | CTTATTGTTGTCATT[C/T]TGCTAGGTATCAGTT | 92912 |
rs146752649 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861623 | GTCTTGAGTCTTGTA[C/T]CTCATATTATTTCTA | 92912 |
rs146866226 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881116 | ATTCATATGGGGGAA[C/T]GAATAAAGCACCCAG | 92912 |
rs146966800 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894411 | ATCTCTGTAAAAAAA[A/C]CAAAACAAAACAAAA | 92912 |
rs146982924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889295 | AAGGTCCCAGGGTTT[A/G]GGCAAAGCAAGTGGG | 92912 |
rs147300807 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858034 | GTCCTCTGGGAACTG[A/G]TAATCTAATGGAACT | 92912 |
rs147317833 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853093 | AAAATCATACAAAGT[A/G]ACAGAGTAAATGTCT | 92912 |
rs147380603 | in-del | -/ATA | 0.00597247 | 0.0543191 | cds-indel, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900028 | AATTGTTTCCTGAAG[-/ATA]ATACTCTTAATTGAG | 92912 |
rs147408034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883552 | AGTGATCCTCCCACC[C/T]TGGCCTCCCAAAGTG | 92912 |
rs147557998 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849253 | TCGTTCTCCACCCCA[C/T]ATTTATTGAACAGCA | 92912 |
rs147679149 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867396 | CTGTGACTTTCTCAA[A/G]CCCAGCAGTCTGATT | 92912 |
rs147763801 | in-del | -/TCTTT | 0.0558544 | 0.157504 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858995 | TTCTTTCTCTTCATC[-/TCTTT]TCTTGGTCAGAGCCA | 92912 |
rs147767676 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900218 | GTTATTTAAAATACT[A/G]AGTCATCTTACGTTT | 92912 |
rs147783876 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894241 | AGAATGAAAATGAAT[C/G]AAGCCTCTGATTGTT | 92912 |
rs148047148 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851281 | TTTTTTTGTAGAGAC[A/G]GGGTTTTGCCATGTT | 92912 |
rs148223785 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846393 | CAGGTTTCCGCCGCC[A/G]CACCCGGCTAATTTT | 92912 |
rs148226538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882662 | ACTGTTGTTAAGTTG[A/G]TATCTTGTGTCATTA | 92912 |
rs148273535 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890562 | TTGTAAGTAGAAAAT[C/T]CTTTAATAGCTCCTA | 92912 |
rs148306202 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856209 | AATGTATATATATAT[A/G]TGTGTGTTTATACAT | 92912 |
rs148412433 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858487 | TGACCCCCGCCCCCC[A/G]CAAACTAGTAATTTT | 92912 |
rs148446417 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865159 | GAAACCTTCTGCAGG[C/T]TTCTTCCTGATCACT | 92912 |
rs148457897 | in-del | -/TTG | 0.293294 | 0.246223 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872878 | CTATTCTTTTTTGTA[-/TTG]TTTTTCATTTTAAAG | 92912 |
rs148486834 | snp | A/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842234 | AGGTTGGACGCATAT[A/G]CAGCTGGTCCTGCCT | 92912 |
rs148533753 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879857 | AGCAGTAAAACTGCC[C/T]AAAGAGGAAAACTGT | 92912 |
rs148604284 | snp | C/T | 0.000215985 | 0.0103897 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854458 | ACATCAGTTCTGGAA[C/T]GTCTAGAAGATACTA | 92912 |
rs148689378 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871398 | TTCCTCAGCACAGAC[C/G]CTTTACGGGTGTCAG | 92912 |
rs148749625 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848354 | ACAAAGGAAATAAAC[C/G]TGGACTAAGGAGCCT | 92912 |
rs148852252 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850918 | ATAAATGTGCTTTTA[C/T]GAAACAAAATTTTCT | 92912 |
rs148920865 | snp | G/T | 1.65581e-05 | 0.00287728 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890460 | GGTGGAGGAGCATTA[G/T]GTATGGAACTTCTCA | 92912 |
rs148960035 | in-del | -/AAAG | 0.0115144 | 0.0749975 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854924 | TTGTTTTTAGTATAT[-/AAAG]AAATATAACTTTCCA | 92912 |
rs149007950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845415 | AGTGGAAAACAGAAA[A/G]TGTAGTAGTTGTCAT | 92912 |
rs149116075 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882540 | AAATAATAGGAGGTT[-/A]AATGAAATTGTACTT | 92912 |
rs149221595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893093 | ATTAGAATTACACTA[C/G]AAAGTGAGAGAAATA | 92912 |
rs149261664 | in-del | -/T | 0.0372196 | 0.131242 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898815 | GAATAAAACTTATTC[-/T]TTTAGTCTAATATTC | 92912 |
rs149319303 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841980 | AATAAAAACTTTCAG[C/T]AGACTTAATGTGTCC | 92912 |
rs149335750 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895356 | CGCCTGGCTAATTTG[A/G]TATTTTTGTAGAGAC | 92912 |
rs149389551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852525 | AATATGGTTTTGAGG[A/G]GTTTCAGTCCAGAGT | 92912 |
rs149444246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858242 | GAGTTTCAAACCCAT[A/G]TATCTGTCTGTAAAT | 92912 |
rs149445340 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864165 | TTTACTTCTATATTA[A/G]GTAAGGTTATACTTT | 92912 |
rs149829593 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844913 | AAAAACCTTGATGTT[A/G]TAATTGACCTTAAAA | 92912 |
rs149839773 | snp | C/T | 6.68874e-05 | 0.00578267 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75879155 | AAAAGAAAAAGAAGG[C/T]ATAGAATATATTTTG | 92912 |
rs149859498 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899473 | AATGTGTTGACTGTT[G/T]TATGTTTGGACTAAT | 92912 |
rs149913025 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853961 | CCATCAGAGGGAGCA[A/G]TGGAAAGAGCAGGAG | 92912 |
rs149919651 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870616 | AACCTAGAAAGGTAG[A/T]CTGGACTTTGGAGAT | 92912 |
rs149980560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866818 | TGCTTGCATAGTAAT[C/T]TGTTTTTTATTTTGT | 92912 |
rs149988735 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885017 | AATATTTCTTAATTT[A/T]ATTTTTTTCAGTATT | 92912 |
rs150041960 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892536 | TGAAGAAGACCTGAA[A/G]AGAAAATGGATGAAA | 92912 |
rs150142857 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895246 | TGGAGTGCAATGGTA[C/T]GATCTCGGGCTCACT | 92912 |
rs150241829 | in-del | -/CT | 0.00557542 | 0.0525036 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866994 | ATACCTGGTTATCTC[-/CT]CATTTATAGATGAGA | 92912 |
rs150289149 | in-del | -/T | 0.4944 | 0.0526182 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891485 | CTTACCAAGTTTTTT[-/T]TTTTTTAAATCTTTT | 92912 |
rs150350007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847367 | GTAAATTGACTTCAT[A/G]TGAGAGTGTAAGAAG | 92912 |
rs150385032 | snp | A/G | 0.000695676 | 0.0186374 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860015 | TAGTGTTCAAGAGCT[A/G]AATAAATTGTCTCAA | 92912 |
rs150419757 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857301 | AGATCTAAAGATAAC[A/G]GTTTTGTAATAGCAA | 92912 |
rs150453894 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873953 | TCCCATCTTGGCCTC[C/T]GAAACTACTGGGATT | 92912 |
rs150555936 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876745 | CATTTCCTTGTTTGA[C/T]GAGTATTCTTACTCA | 92912 |
rs150615997 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852292 | TGTTACCGCCTTTAT[G/T]TGTGCTAAAGTGCCA | 92912 |
rs150625550 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890643 | AAAGGTAAACCAATA[A/C]AATGACATTGTACTT | 92912 |
rs150678334 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899012 | CACCTGTAATCCCAG[C/T]ACTTTGGGGAGGTGG | 92912 |
rs150727029 | snp | A/C | 0.00015099 | 0.00868748 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854471 | AACGTCTAGAAGATA[A/C]TAAGAACAACAATTT | 92912 |
rs150819039 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884614 | ACATATGGATATGCT[A/G]AGCTCATTTTGAGTT | 92912 |
rs150896299 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863854 | ACCATGTTGGCCAGG[C/T]TGGTCTCGAACTCCT | 92912 |
rs150997072 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866022 | TTGAGTCTATTCCCA[C/G]TTCTTTACGCTTTTA | 92912 |
rs151067108 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880753 | GTACACTTCCCTTGG[C/G]CTTCCAAAGTGCTGG | 92912 |
rs151121237 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887523 | GGAAATAGTGCTGAT[A/G]TAATATCTTGTACTT | 92912 |
rs151153250 | snp | A/G | 0.00915586 | 0.067038 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853504 | ATTATATATATATAT[A/G]TATGTATGTATGTAT | 92912 |
rs151262694 | snp | C/T | | | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75873488 | ATTAGTGGGAAAAAG[C/T]CAGAGGATGAAGGAA | 92912 |
rs180681326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887187 | ACCAAAGCCAGCTAT[A/G]TAAGAGGGGATTAAA | 92912 |
rs180689365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867491 | ATTTGTTTTTCTGCT[A/G]CTGCGGCAGACCTAC | 92912 |
rs180689572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896040 | AAACAGGTATGTTCT[A/G]TACTGATAAGGAACA | 92912 |
rs180694421 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877142 | CTCCAGCCTGGGCAG[C/G]AAGAGTGAGACTCTG | 92912 |
rs180699031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851258 | ATCTTACTGGCTAAT[C/T]TTTTGTATTTTTTTG | 92912 |
rs180703090 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859103 | AAAACATTTTAAACA[A/G]TGAACACCATACTTG | 92912 |
rs180947523 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873897 | AGATGAGGACTCTCT[C/G]TTGCCCAGGCTGGTC | 92912 |
rs180952023 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900169 | TGTTGGTTCAGTGTT[C/T]CTTATGAACAAGAGC | 92912 |
rs180953955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855876 | ATGTCACTTATCGCC[A/G]TGTCTTCATATTCGT | 92912 |
rs180976745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892278 | AGCCTGTAGGATTCC[C/G]AAAGATTAAAAGAAT | 92912 |
rs181105045 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850336 | TTATGTGTGTTCCCT[C/T]TCCCTTAAAAAATCA | 92912 |
rs181311539 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883310 | TAAAATCTTCTAAAT[A/G]GTATAACACTAAGGA | 92912 |
rs181397653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872459 | TAAGAACAGATAGTA[C/T]GGGAAAGAAGGGAGC | 92912 |
rs181409000 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854597 | AATGATTATAATCTT[A/G]TAGGAATTAAAGACT | 92912 |
rs181426169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891217 | ATCACTTAATGATTT[C/T]GTATCTGTTTTTAGT | 92912 |
rs181438530 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855351 | TAAAAATTAACTGGG[A/C]ATGGTGGCGCATGCT | 92912 |
rs181476804 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900602 | ATTTTTCTGCACAAA[C/G]AAGTTACAAAGTTCA | 92912 |
rs181570946 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872784 | AGAGATAACTAAGAT[G/T]AACTGAAATTAACAT | 92912 |
rs181605447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886559 | TCAAGGAAAAGATTT[A/G]GAAGAAATTTGCAAA | 92912 |
rs181614068 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882617 | TATAGATGAAAGGTG[A/T]GCTACTTTATTTGAA | 92912 |
rs181614480 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867346 | ATGTCTGATTCTTCT[A/G]AAAAAAAGTGGTCCC | 92912 |
rs181633591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845276 | AGGGCATTTTAGACT[A/G]AGGAAACTCCACCCA | 92912 |
rs182014107 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844861 | CTTTGGTTGAGTCAG[G/T]GGGTACTCAAGTGCC | 92912 |
rs182026119 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849505 | TATGGAGAAAAATAG[A/T]TACAGAAAGTTACTT | 92912 |
rs182046777 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879042 | TTTTTGAGTTTAGTT[A/T]AAAAAAAAAATCTCT | 92912 |
rs182194797 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898391 | ATTTTTTTGTTATTT[A/T]AAAAAAATAGATATT | 92912 |
rs182196693 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880108 | TTTAATAAGGTTTTT[G/T]TTTGTTTGTTTGTTT | 92912 |
rs182202420 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860504 | ACCACCCACTTACCA[C/G]TCACCTCCCCTTCCT | 92912 |
rs182203982 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885120 | ACTAATAGTAGTGGG[G/T]TTTTTTTTTATTTGT | 92912 |
rs182230333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895292 | TGGGTTCAAGCGATT[C/T]TCCTGCCTCAGCCTC | 92912 |
rs182234951 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875416 | TTTCATCTTTAGAGA[C/T]GTCCCTGCACTGAAA | 92912 |
rs182245055 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857915 | TATACTTTTTTCTTT[C/G]CTGGTGGGTACAGGA | 92912 |
rs182293017 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863468 | CTTTTTTTTTTTTGA[C/T]GGAGTCTCTCTGTCG | 92912 |
rs182300840 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859437 | TTTTTAAATGAATAT[G/T]ACTGGAATATATAAT | 92912 |
rs182301183 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885149 | GTTTTTTGAGACGGG[A/G]TCTCACTGTCACCAG | 92912 |
rs182572168 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866993 | GATACCTGGTTATCT[C/G]CTCATTTATAGATGA | 92912 |
rs182631258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883824 | TAATGATTCATACAC[A/G]CATGTATTTATACAT | 92912 |
rs182642413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847807 | GAATGAAAAATCTCC[C/T]CCAGGAAGTAAATTA | 92912 |
rs182662253 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864561 | CCTTTTTCTATGTAT[C/T]GGTCTCCAGATTTTC | 92912 |
rs182671741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846035 | CAGCTGCTCAGTACA[A/G]ATGTCTGCTAACTTT | 92912 |
rs182852078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874441 | GGTGTACACCACCAC[A/G]CCTGGCTAATTTTTG | 92912 |
rs182863814 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856417 | AACCAGATGTTCAAT[A/G]AAATGTTGTATACTA | 92912 |
rs182914641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865514 | GGTACCCCTGTGCCA[A/G]CATTTCTCTGGGGCA | 92912 |
rs183036099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848299 | ATCTTGCATTTTTCT[A/G]GTCTTTACTATGATT | 92912 |
rs183037930 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892772 | TCTCAGCTACTCAGG[A/T]GGCTGAGGTGGGAAG | 92912 |
rs183075697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888501 | CCATATATATGGCAT[G/T]TTATCCTTAGATGAC | 92912 |
rs183079699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870113 | CTCACTGTGGTGCAG[G/T]CTGGAGTGCAGTAGT | 92912 |
rs183088833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852695 | ATGGTGTATTCCCAA[C/T]GTGTGCTGAAGAATT | 92912 |
rs183121697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893600 | TAATAGACAAATATA[C/G]ACCTCTGTACCCAAT | 92912 |
rs183135816 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857604 | AAACTAGCGGCTCCT[C/G]TCTTAGTCCCCAAAT | 92912 |
rs183377042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898746 | TCGCCAGGATTTTGT[C/T]TGGGGAAATAAGTAC | 92912 |
rs183387747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875112 | TTCCAGTTTGAGTTA[C/T]AGTCAAAACAACTAT | 92912 |
rs183423766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866003 | TAGAATTCTAAGTTC[A/T]TAATTGAGTCTATTC | 92912 |
rs183517279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869441 | AAAGAATTTTGTCTT[A/T]ATCTGGTTTACACTA | 92912 |
rs183517905 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879684 | GTCTGCTGCCCTCCA[A/G]AGGGCCACAGAACAT | 92912 |
rs183527850 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851559 | TGTTCAAAAACTTGC[A/G]TTTTATTATTAGCAG | 92912 |
rs183641845 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884281 | AAATCTAAATATATC[C/T]AGCCTTTCCTTTGAT | 92912 |
rs183725767 | snp | C/T | 1.65064e-05 | 0.00287279 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899488 | GTATGTTTGGACTAA[C/T]GTTGCTTTAAAGAAA | 92912 |
rs183731534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897880 | AGTTTGTGACTTAAG[A/G]TTTGTGTTTTGTGCT | 92912 |
rs183742620 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882129 | AGGTGATTTTCAACT[C/G]AATGTGAGGAAGCGA | 92912 |
rs183747550 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863162 | TCTGGGGTACCTAGT[A/G]TCTGAGTCTAGAGCC | 92912 |
rs183750720 | snp | A/G | 0.000447572 | 0.0149528 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859882 | GTGTTTTGTAGCTTC[A/G]TCAGCAATTGAAGTG | 92912 |
rs183755387 | snp | C/T | 0.000907304 | 0.0212798 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844326 | TCAGCCAATTGTTTT[C/T]AAGTTTGCGTTTAAG | 92912 |
rs184018712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861854 | TCTCATTTGGCAGCT[C/T]TCACTATGTGGTTTA | 92912 |
rs184033459 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888056 | ACTTCTTTATTTCTT[G/T]ACATAGCCAAACATT | 92912 |
rs184061276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884807 | TGGGATGCCACCATG[C/T]CCAGCTAATTTTTGT | 92912 |
rs184160826 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880415 | ACCACACCTGGCCTA[A/G]TAAGTATTTTAAAGA | 92912 |
rs184272985 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866469 | TGAGCCACCGTGTCC[A/G]GCCTTCAGTATTCCT | 92912 |
rs184279135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848763 | TGAGTTGAATGGAGA[C/T]AGTCACTGCCAAATG | 92912 |
rs184285004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885359 | TTGACCTCGTGATCC[A/G]CCTGCCTCAGCCTCC | 92912 |
rs184289442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867173 | CCTGAGCTAAAAGGA[A/G]GAGGTGGAGTCTAAG | 92912 |
rs184290506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895434 | GTGATCTACCTGCCT[C/T]AGCCTCTAAAAGTAC | 92912 |
rs184297050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849516 | ATAGATACAGAAAGT[C/T]ACTTCTAAATAAGAC | 92912 |
rs184327076 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870806 | AAAAGGCAGATGGTT[A/T]AAAGTCTTGAATTCG | 92912 |
rs184344390 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890752 | AACATTGGTTTGTTG[G/T]TTTTTTTTGTGAGAT | 92912 |
rs184344663 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872611 | GCATGATCATAGCTC[A/T]CTGCAGCCTCAAACT | 92912 |
rs184372843 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884908 | ACCCGCCTCAGCCTT[C/G]CAAAGTACTGGGATT | 92912 |
rs184384026 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849258 | CTCCACCCCACATTT[A/G]TTGAACAGCAAACTA | 92912 |
rs184435584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889160 | AAGATAGATTTCTAT[A/G]TTTCAGAAATAGAAT | 92912 |
rs184458649 | snp | C/T | 0.00132217 | 0.0256775 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853439 | TTGTGCCATGCACTC[C/T]GCCTGGGCCACAGAG | 92912 |
rs184506554 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866649 | TCTCTTCTGTTTTCT[C/T]CCCCATCTCCTTTTT | 92912 |
rs184581050 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842653 | GCAGCCCTAGCTCCA[C/T]GGGGGTGTGGGTGGG | 92912 |
rs184594474 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889419 | TAATGTTAGTGGTCT[A/T]CAGTAAAAGTTTTTA | 92912 |
rs184608740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871684 | TTTCAGAGAGCATGG[A/G]GTTGGGGGTAAGGTC | 92912 |
rs184629933 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895677 | CTCAATAGAAATACA[A/G]ATCAAAACTATACTG | 92912 |
rs184639711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858894 | CATTTTCATTTGCTC[C/T]GTTGTCCACTTTGGG | 92912 |
rs184779306 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876736 | TAAAGTTTTCATTTC[C/G]TTGTTTGACGAGTAT | 92912 |
rs184795798 | snp | C/T | 1.66305e-05 | 0.00288357 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854405 | CCTATCCATCTTCTT[C/T]ACCGATATGGTTTGT | 92912 |
rs185002440 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75864668 | TTGCATCATATTCAC[A/G]TGTGGCTATATGCCG | 92912 |
rs185010236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846105 | TGTAATGTAGCCAGC[C/T]TCAACAATGATAAAC | 92912 |
rs185134624 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875936 | CTGGGCGTGGTGGTG[C/T]GCACCTGTAGTCTCA | 92912 |
rs185206832 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881251 | TTTTTTTTTTTTATC[C/T]GTCCCTGTGGCCCCC | 92912 |
rs185258002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858469 | TTATATACTACTGTT[C/T]TCTGACCCCCGCCCC | 92912 |
rs185306682 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898916 | CATAGAAAATAACTT[C/T]CTGTTGTGAAATAGC | 92912 |
rs185313474 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877321 | GTGCAGGATAAGCCA[A/G]ACTTGTTTCTGAGTT | 92912 |
rs185320732 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860192 | CTATACAGGCAAACA[A/G]TTGCCCTTCTCTCTA | 92912 |
rs185322354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862294 | TGGTTATTTTTTATT[A/C]ATATTCTATTTTTGT | 92912 |
rs185327040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886626 | GATGTGGTTGCTCAC[A/G]CCTGTAATCCCAGCA | 92912 |
rs185327568 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859219 | CTTTGCAGTTTTCCT[A/T]GTGAATTATTGTTAT | 92912 |
rs185335807 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867355 | TCTTCTGAAAAAAAG[A/T]GGTCCCTGCATTATT | 92912 |
rs185344857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75850828 | ATGTAAGTTACGTCT[A/G]TTGGTATTTATCACT | 92912 |
rs185425710 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900185 | CTTATGAACAAGAGC[C/T]ACAGTACAGAGCTTC | 92912 |
rs185506973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896047 | TATGTTCTATACTGA[C/T]AAGGAACATTCTCCA | 92912 |
rs185562039 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882578 | CTTACATCAACCTCT[A/G]TACCTTTCATTATGT | 92912 |
rs185868838 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863799 | AGGTGTGCACCACCA[C/T]GCTCGGCTAATTTTT | 92912 |
rs185876967 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845561 | TGTAGGCTGTGGGGA[G/T]CTACTAAGTTTACTC | 92912 |
rs185886796 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872804 | GAAATTAACATTTCA[A/T]TGTAAGTTCTTCTGG | 92912 |
rs186012519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891632 | GACAAGTGGCAGAAC[A/G]AGGATTGGAACTAGA | 92912 |
rs186031137 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855528 | ATTTTCCCATGATGT[A/C]ATACAGTCTTTATAG | 92912 |
rs186131227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887255 | TGGACTTAATTTATC[A/G]GAGGTTTAAAGCAGC | 92912 |
rs186152221 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851276 | TTGTATTTTTTTGTA[C/G]AGACAGGGTTTTGCC | 92912 |
rs186187914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897998 | GAAGAGAGAAACGAT[A/G]AAATTTGAGGACAAG | 92912 |
rs186253855 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892817 | GGAGACCGAGGCTGC[A/G]CTGAGGCATGTTTGC | 92912 |
rs186278643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867832 | TCTTTGGGAGTTTTA[G/T]GCTAGGTATATAGTC | 92912 |
rs186311391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892463 | TATGTGAAATCTAAT[A/G]TAAAGAAAAAAAGAT | 92912 |
rs186321191 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874200 | CGACAAAATACAATT[C/T]AAGTTCTTTCTCCTT | 92912 |
rs186351039 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879699 | AAGGGCCACAGAACA[G/T]AAACAGATATACGAT | 92912 |
rs186672696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879292 | AGATACTCATACCCT[A/G]TGGTTCAGGAATCTC | 92912 |
rs186786847 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898443 | TTGAAGTATACATAA[C/G]TGTGGAATGACTAAA | 92912 |
rs186803305 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880112 | ATAAGGTTTTTTTTT[G/T]TTTGTTTGTTTGTTT | 92912 |
rs186807820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861058 | CTAATTGCTCTATGC[A/G]TCAATTTTCCATTGG | 92912 |
rs186883351 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897269 | TTTGAGACGGAGTCT[C/T]GCTCTGTCACCCCAG | 92912 |
rs186897389 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859466 | ATTTTGTAATCCATC[C/T]GTAACAACACTGCCT | 92912 |
rs186968304 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882840 | CAACCTAAGGAGCCG[A/G]AGACTTAGCAGGGCC | 92912 |
rs186999286 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888869 | CTGCATCCTCAAAGG[A/G]AGAGTGGGGTACCTT | 92912 |
rs187063682 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863594 | GGGATTACAGGCACA[A/T]GTCACTACGGCCAGC | 92912 |
rs187153820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874752 | AAATGATGTGTGTAT[A/G]TATATAAAATGCTCA | 92912 |
rs187158263 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75901216 | GATTTAACAAGAGAA[A/G]GTGAAAGTGTGAAAG | 92912 |
rs187238443 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884897 | GAAGCCATCTTACCC[A/G]CCTCAGCCTTGCAAA | 92912 |
rs187248672 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866614 | ATCTTCAATGTCCCT[G/T]AACTGTTCTCTTACT | 92912 |
rs187263895 | snp | A/C | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845042 | TGAGTGTTCTGGGCA[A/C]TAGTGTTGCAGAATT | 92912 |
rs187440959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888144 | GTACAATTTGGTGGT[C/T]GTTAGTATATTCACA | 92912 |
rs187445794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869447 | TTTTGTCTTAATCTG[A/G]TTTACACTATTTTAA | 92912 |
rs187448757 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851834 | AAAAAGACATATTCA[A/G]GGATTCAGATGTAGT | 92912 |
rs187545888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895294 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC | 92912 |
rs187548890 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875546 | CTCTATTTTAGTAAA[G/T]AATGTGTCACCTTGA | 92912 |
rs187558265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857926 | CTTTCCTGGTGGGTA[C/T]AGGAAACTGTCAATA | 92912 |
rs187645181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884594 | TTTTTTTAACCTTTC[A/G]TATTACATATGGATA | 92912 |
rs187654753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866153 | TCTGTAACTGTAAAG[C/T]GTGGGGGTTTTACTT | 92912 |
rs187660368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848348 | AGTTGTACAAAGGAA[A/G]TAAACCTGGACTAAG | 92912 |
rs187717980 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889180 | AGAAATAGAATACAC[A/G]AAAAAAAATTTAATC | 92912 |
rs187732417 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853602 | CATTAGAATTTTATG[G/T]TATTTGAATTACTTT | 92912 |
rs187772447 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857724 | AATAAAAATCATAGT[A/G]TATAGTTTTATAATA | 92912 |
rs187809817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870621 | AGAAAGGTAGACTGG[A/C]CTTTGGAGATGTCAG | 92912 |
rs187978571 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899226 | GTTGCAGTGAGCTGA[G/T]TTTGCGCCATTGCAC | 92912 |
rs188011904 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871049 | ATTTGTAGGTGTTTC[C/T]CCGAGAGGGGGATGT | 92912 |
rs188069501 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848983 | GTTTGCTTACAATGA[C/T]GTTCTCAGTAGCTGT | 92912 |
rs188079585 | snp | G/T | | | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875205 | CACATTTAGTCTTCA[G/T]AGCCACCGTGTGAAA | 92912 |
rs188102275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853048 | GAAGCTAATATACGA[C/T]AATAATGGCTTTTCC | 92912 |
rs188281551 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841332 | AATTTAAAAAGCTCT[A/G]TTTTCTCACAGCAAT | 92912 |
rs188355530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893741 | TTTAAATATGAAGCA[A/G]TTAAGGTTAGAAGGC | 92912 |
rs188397284 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899626 | TAAGTTACAGCCTTT[A/G]CATTTTGCTCATTTT | 92912 |
rs188411782 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882368 | TTTTTATTTCTGTAA[A/C]ATCTGGATTCCTGAG | 92912 |
rs188413904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863233 | AATATCCCCCTAACC[C/T]CCACCTTTGTTGGCT | 92912 |
rs188482488 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881691 | GGCCTCTGATGTCCA[C/T]GGTGACAACTTGAAT | 92912 |
rs188494687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863013 | TCTGTGTTCTTTTGC[A/C]TGAGGTAGATGTATG | 92912 |
rs188502870 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842689 | TTATCTTAAGCTTGG[A/G]AAACAAGGCAAAATA | 92912 |
rs188563659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856716 | TAGGAGGCCCAGGCA[A/G]GCGGATCAGTTGAGG | 92912 |
rs188620428 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865663 | GTCAGAGAATATGGC[C/T]TGTGACCTTTCAGCT | 92912 |
rs188743550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859075 | ATCCCATTTGAGTCA[C/T]GTTATACATTGAAAA | 92912 |
rs188859926 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880805 | TGGATCTGGATGAGA[G/T]GTAATGGTTTAAAAT | 92912 |
rs188889914 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883875 | ACACACGTATATATA[C/T]GCACATACTTTTTAC | 92912 |
rs188904140 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847814 | AAATCTCCCCCAGGA[A/G]GTAAATTAGCTAGTA | 92912 |
rs189052027 | snp | A/C/G | 0.00795532 | 0.062565 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885951 | AAATATTTACATATA[A/C/G]AAAATAAACACAAGA | 92912 |
rs189054119 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867213 | CTGCATTGAGTTATA[C/G]TAAAAACACTCTCTG | 92912 |
rs189136723 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898812 | GTGGAATAAAACTTA[C/T]TCTTTTAGTCTAATA | 92912 |
rs189146901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862149 | CAAATTCTGTAGGTT[A/G]AAGTGAGTCTCAGGG | 92912 |
rs189278014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892241 | ACACAGATACTTTTT[A/G]TAGGAAAGCATCTCT | 92912 |
rs189382176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890218 | TCTAAGAACCATTAG[A/G]AAAAATTGACTAGAA | 92912 |
rs189395301 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871721 | TAACAGAATCTCAAG[G/T]CAGAAGAATTTTTCT | 92912 |
rs189399214 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854545 | ATTACATATAGAAAT[G/T]AAATGTTAAGAGATA | 92912 |
rs189430723 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896877 | TTAAAATTGTTTTTG[A/G]AATGGAGATAGTCAG | 92912 |
rs189452479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859363 | ACTCAGGGAATTAGA[C/T]AGGATATCCAAGGTC | 92912 |
rs189565108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872745 | ATAAAACTTGGAAAT[G/T]AGGGGAAAGCATTAA | 92912 |
rs189598270 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844786 | TTATAATAGGCGTCA[A/G]GGTGGTGGCTTCGGG | 92912 |
rs189599506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883491 | TTTTTTTATAGGGAC[A/G]AGATCTCACTATGTT | 92912 |
rs189641636 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876761 | GAGTATTCTTACTCA[A/G]TATGACTTGAATGTT | 92912 |
rs189821769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891101 | TTGACTTAATTCTTT[G/T]TTGAGATAGTTTCAT | 92912 |
rs189843871 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855212 | AAAACATTTACTGGC[C/G]AGGTGTGGTGGCTCA | 92912 |
rs189888695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895904 | AGTACTCAGCAGATA[C/T]ACGTACAAGGTTGCT | 92912 |
rs189964783 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855637 | TTTTAAGATTACTGG[A/T]TGAAAGCTCTGTTAC | 92912 |
rs190045790 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877848 | GCTTAGTTGTTCCAT[C/G]TTTTAAGAGCAAAAT | 92912 |
rs190075081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883101 | CTATCATTATTGGAA[C/T]GGTTCCTTTATATAG | 92912 |
rs190089792 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845562 | GTAGGCTGTGGGGAG[C/T]TACTAAGTTTACTCA | 92912 |
rs190114627 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895603 | GGGGGTATAAAAAGT[C/T]TGTTTACAGAAATAG | 92912 |
rs190119743 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879955 | TGTGAACTGAAAGGT[A/G]TATCTGCGCAGGCTT | 92912 |
rs190131115 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75860406 | ATCACTAATTTCATT[C/G]TGGATTTACCTATTT | 92912 |
rs190131542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858618 | GAAAATTGAAATTCG[C/T]GGAGAGTGTACTACC | 92912 |
rs190140775 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886865 | GAGAGTCCGTCTCAA[A/G]TTTTTTTTTTTTTTA | 92912 |
rs190189254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866676 | TTTTTTCTCTGTTCT[A/G]AGGAAATGTCACTGT | 92912 |
rs190372494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875937 | TGGGCGTGGTGGTGC[A/G]CACCTGTAGTCTCAG | 92912 |
rs190435802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882603 | TTATGTCTGTTAAAT[A/G]TAGATGAAAGGTGAG | 92912 |
rs190445780 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849267 | ACATTTATTGAACAG[C/T]AAACTATGAAAGTAA | 92912 |
rs190450057 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845262 | GGAAGGCTGGCGGAA[G/T]GGCATTTTAGACTGA | 92912 |
rs190511592 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75888244 | GATTAGCAGTCACTC[C/T]CTGTACCCGTTTCCC | 92912 |
rs190524107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75869802 | GTGCATTCCAAAGAC[A/G]TTGAGCTTAGGCCAG | 92912 |
rs190531438 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852470 | TTTCATCTACAAGAT[C/T]AAAAACATGATTTCA | 92912 |
rs190626828 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884915 | TCAGCCTTGCAAAGT[A/G]CTGGGATTACAAGTC | 92912 |
rs190668989 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900319 | CCTTGAGCAAAAGCT[G/T]TGCAGTTAAGTACAA | 92912 |
rs190679673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865507 | ATTTCATGGTACCCC[C/T]GTGCCAGCATTTCTC | 92912 |
rs190690894 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863603 | GGCACATGTCACTAC[A/G]GCCAGCTGATATTTT | 92912 |
rs191056615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892626 | ACACTTTGGGAGGCC[A/G]AGGCAGGAGGATGGC | 92912 |
rs191062292 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874380 | CTTCCACCTCCCAGG[A/T]TCAAGCAGTTCTCCT | 92912 |
rs191074890 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856350 | TTGACAAAATGACTC[C/T]AACATTTGTTTAAAA | 92912 |
rs191126811 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75874970 | TTCAGTCTAATTTAT[A/G]TATTAATCTAATTTA | 92912 |
rs191131167 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846785 | TATACTTACCAAGAA[A/C]CATCCTTATGCAGTT | 92912 |
rs191133878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873139 | CTAAACTGTTTTAAA[A/G]GTTCCTCTTAATAGG | 92912 |
rs191155045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2Q2 | GRCh38.p7 | 15:75875252 | TTTAGAGATAGGAAA[A/G]ACTTCTCATATTTTG | 92912 |
rs191160831 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857754 | AGAATATTCTGTTGT[A/T]GGCAAAAAAAAAAAA | 92912 |
rs191236691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851046 | TATTTGCTTGAAATA[A/T]TGTAAACAAAATCCA | 92912 |
rs191362558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75893501 | ACCATCACAGTTGGA[A/G]ATTTCAACATACCCT | 92912 |
rs191380264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75857351 | ATCTAAAATATTACA[G/T]AAACATGTTCATAAG | 92912 |
rs191431630 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898279 | TGCTGTATTTGAGAG[C/T]GTGTGGGTATGTGTA | 92912 |
rs191463548 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75867393 | AGTCTGTGACTTTCT[C/G]AAGCCCAGCAGTCTG | 92912 |
rs191474832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897270 | TTGAGACGGAGTCTC[A/G]CTCTGTCACCCCAGC | 92912 |
rs191698732 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859683 | TGTAGTGATTATACC[C/T]CAAGCCATAGTAACT | 92912 |
rs191716683 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884668 | ATTTATTTTTACTTA[C/T]TTATTTATTGAGATA | 92912 |
rs191724520 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866314 | GAGTAGCTGGGACTA[C/T]AGGTGTGCACTGCCA | 92912 |
rs191727876 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879554 | CCTTTATATACAGTT[A/C]AAAAATAGGTAAAAC | 92912 |
rs191730420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848532 | ACCAATTTATAATAT[A/G]GGGTCAAATTCCTGG | 92912 |
rs191915439 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890312 | CCTAACAACTGTTGT[A/C]ATGTTTGCATGTTAT | 92912 |
rs191925341 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899250 | ATTGCACTCCAGCCT[A/G]GGTAACAGAGTGAAA | 92912 |
rs191928976 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75881896 | GGTCTATTTAGATAA[A/G]CTTAGGTTCATTTAG | 92912 |
rs191932805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868477 | TTTTGTGAAATGTCT[A/G]TTATCAATAACACAT | 92912 |
rs191936710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863075 | AGAACAGTGTGTTTC[A/G]GGGCCTGGAAAATGT | 92912 |
rs191949328 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UBE2Q2 | GRCh38.p7 | 15:75843473 | TTACAAAGGAAGCGC[C/T]ACCCAGGCCGCCACA | 92912 |
rs191966813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884219 | GAATGTTCCAACACT[C/T]GGGTGACTAATTCTA | 92912 |
rs192186104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866617 | TTCAATGTCCCTTAA[C/T]TGTTCTCTTACTTAC | 92912 |
rs192187730 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894429 | AAACAAAACAAAACA[C/T]GAAAATTAGCTGGGC | 92912 |
rs192238449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887490 | CAAGGAGGGTAGGAC[C/T]CATGTAGAAGAGTTT | 92912 |
rs192260168 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851515 | TGGAAAACGGTGGTG[C/G]ATACAAGTTTTCAAA | 92912 |
rs192308973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865988 | TGATGGAGCTAGATA[C/T]AGAATTCTAAGTTCA | 92912 |
rs192423680 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898717 | ATAACAGTCCAAGTT[C/T]CTTGTATTCTAAATC | 92912 |
rs192427599 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853697 | TCAGGATTTTGTGCA[A/G]TTTACCTTGGGTTCA | 92912 |
rs192437427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880367 | ATCTGCCTGCCTCGG[C/T]CTCCCAAAGTGCTGG | 92912 |
rs192439982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75861321 | TGTCTTCTAACCAGT[C/T]GTGGTGGTGAAGCCT | 92912 |
rs192574153 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884907 | TACCCGCCTCAGCCT[C/T]GCAAAGTACTGGGAT | 92912 |
rs192590770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75849047 | TTCTTTTTATCATGG[G/T]TATATGAACATTTTT | 92912 |
rs192632057 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876474 | TTTTGGATTTTTAAA[A/C]AATGTTTTTATAGGT | 92912 |
rs192689683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895382 | GAGACGGGGTTTCTC[C/T]GTGTTGGTCAGGCTG | 92912 |
rs192696542 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875850 | GCAGACCACGAGGTC[A/G]AGAGATTGAGACCAT | 92912 |
rs192700037 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858244 | GTTTCAAACCCATAT[A/G]TCTGTCTGTAAATCA | 92912 |
rs192711985 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75853419 | GAGGTTGCAGTGAGC[C/T]GAGATTGTGCCATGC | 92912 |
rs192798599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889029 | CCGATTATTAAGCTT[C/T]CAGCAATTGTGGAAC | 92912 |
rs192826229 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75898878 | ACAGAGCTCTTGTGT[A/T]GAAAACTCAGGTACA | 92912 |
rs192837503 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862152 | ATTCTGTAGGTTAAA[A/G]TGAGTCTCAGGGCCA | 92912 |
rs192865184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895608 | TATAAAAAGTCTGTT[C/T]ACAGAAATAGAAATA | 92912 |
rs192874046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858773 | TTCATTATGCACTTA[G/T]CACGCAATAGAGTGT | 92912 |
rs192915866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870723 | ACATAGTGTGTTTGA[A/G]TTCATTGGATACTTT | 92912 |
rs193041443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75880946 | TTGCTTGGGGATATA[G/T]CTTATGATTGAACTT | 92912 |
rs193048518 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75841673 | GAATCCCCATAAGTA[C/G]AAAATTTTAGATGCA | 92912 |
rs193061846 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871052 | TGTAGGTGTTTCTCC[A/G]AGAGGGGGATGTGTC | 92912 |
rs193102995 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848105 | TTTACTGTGTTTCTG[C/T]GTACTATAGATAATA | 92912 |
rs193233412 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889198 | AAAAAATTTAATCCC[A/G]TGAACCTTCGCCTGA | 92912 |
rs199539808 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854999 | CTCATGAGCAAGCAT[C/T]ATTGAGAAAATTAGT | 92912 |
rs199550490 | snp | A/G | 0.00385285 | 0.0437216 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891044 | AATTTTACATAAACC[A/G]TAAGATACATTTTAT | 92912 |
rs199621484 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75882996 | AAAAAAGATCCTGCT[C/T]TCTGGTGTTCCCTTT | 92912 |
rs199622181 | in-del | -/G | 0.0287284 | 0.116357 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75892707 | ACACAAAAAATACGC[-/G]CCCCCACCCTAAAAA | 92912 |
rs199639053 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854622 | AAGACTAGTTTGTTT[-/G]TTTTTTTTCCTTCAA | 92912 |
rs199640921 | in-del | -/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865818 | GTTTTTTTTTTTTTT[-/T]AACCTAGAAAGGGTT | 92912 |
rs199697694 | snp | A/G | 0.00199806 | 0.0315443 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75897037 | CAATCCTATAATTCC[A/G]TTGTACAGATACATG | 92912 |
rs199802547 | snp | C/G | 1.65081e-05 | 0.00287293 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859947 | CCTAAGCACCTGGAT[C/G]TTGAGATGCTAGATC | 92912 |
rs199867437 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862884 | TGGCCAAGACTGGTA[C/G]CTTTTAGTGGGAATT | 92912 |
rs199898176 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883853 | ATACACACACACACA[C/T]ACACACACACACGTA | 92912 |
rs199933200 | snp | A/C | 8.3194e-05 | 0.00644904 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75868983 | AGTGACTTCAGAAGA[A/C]GAGGAAGAAGAAGAA | 92912 |
rs199957708 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75847132 | TTTATGGTGGCAGGG[A/G]AGAATATTTTATAAT | 92912 |
rs199987692 | snp | C/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842914 | GTGAGAAGGTCCTCA[C/G]AGGAACCCAGGCTAG | 92912 |
rs200041298 | in-del | -/AT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899291 | AAAAATATATATATA[-/AT]ATATATATATATTTT | 92912 |
rs200185992 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75886126 | ACTATTGTGTTTTAG[G/T]TTTTTTTTTTTGAGA | 92912 |
rs200224674 | in-del | -/TAA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891524 | TTAACTCAATCCTCT[-/TAA]TAACTTAAAAAATAG | 92912 |
rs200326388 | snp | A/G | 3.34913e-05 | 0.00409201 | missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854393 | TTAAACAGGAATCCT[A/G]TCCATCTTCTTCACC | 92912 |
rs200341329 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866129 | TTCTGGTAGTTGGTA[-/T]TGATTTTCTCTGTAA | 92912 |
rs200378909 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75855505 | AAAAAAAAAAAAAAA[-/A]TTACTGTATTTTCCC | 92912 |
rs200538631 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887586 | TTTTTTTTTTTCCCC[A/G]TCTGCTAAGTAGACT | 92912 |
rs200604187 | snp | G/T | 0.00120158 | 0.0244816 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879077 | TTTTATTTGAACTGT[G/T]TTTTGTTTTGTAATT | 92912 |
rs200769209 | in-del | -/T | 0.040526 | 0.136457 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854622 | AGACTAGTTTGTTTG[-/T]TTTTTTTTCCTTCAA | 92912 |
rs200781215 | snp | C/T | 0.000165074 | 0.00908348 | synonymous-codon, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859907 | GAAGTGGTTGATATG[C/T]GAACTCTGCAGTTTA | 92912 |
rs200863436 | snp | A/G | 1.65625e-05 | 0.00287766 | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75854421 | ACCGATATGGTTTGT[A/G]GATTCTGAAGACCCA | 92912 |
rs200899461 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883847 | TTATACATACACACA[C/T]ACACACACACACACA | 92912 |
rs200941941 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75884708 | TTTGTTGCTCAGGCT[G/T]GAGTGCAGTGGTGCT | 92912 |
rs201118499 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883619 | GCATTTTTTTTTTTT[A/G]TTCTAAATATAGTGT | 92912 |
rs201134587 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75877183 | AAAAAAAAAAAAAAA[C/T]GGGTTATGACCGATT | 92912 |
rs201169191 | snp | A/C/T | 7.56435e-05 | 0.00614954 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879053 | AGTTAAAAAAAAAAA[A/C/T]CTCTAACTTTTTATT | 92912 |
rs201224317 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883854 | TACACACACACACAC[A/G]CACACACACACGTAT | 92912 |
rs201246404 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890942 | CAGTGCCTACTCAAT[A/G]GAATCGGTCATCATG | 92912 |
rs201262729 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866812 | GAATTGTGCTTGCAT[A/G]GTAATCTGTTTTTTA | 92912 |
rs201380306 | snp | C/T | 5.22516e-05 | 0.00511107 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879083 | TTGAACTGTTTTTTG[C/T]TTTGTAATTCTTAGG | 92912 |
rs201445418 | snp | C/T | 0.000703907 | 0.0187472 | missense, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844420 | TGTTTGAGCGACCCC[C/T]CTCCCCCGGGCCTGG | 92912 |
rs201532128 | snp | C/T | 0.00199802 | 0.0315439 | stop-gained, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75890481 | GAACTTCTCACAAAA[C/T]AGGTGACTTTTCTTA | 92912 |
rs201578261 | snp | C/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75876256 | GACATATACAGATCA[C/G]AGAGTTATAAAACAG | 92912 |
rs201583694 | in-del | -/CT | 0.0232847 | 0.105357 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75866688 | TCTAAGGAAATGTCA[-/CT]GTTTGTTTTTCTTAA | 92912 |
rs201711870 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883851 | ACATACACACACACA[C/T]ACACACACACACACG | 92912 |
rs201764126 | in-del | -/TT | 0.00835141 | 0.0640778 | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899934 | TCATGTCTAAAACCA[-/TT]TTTTATGATATTGCC | 92912 |
rs201793071 | snp | C/T | 0.00140166 | 0.0264361 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843632 | TCCGCGCCCGGCTCC[C/T]CTTCCGCGCCCCTCC | 92912 |
rs201804064 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899226 | GTTGCAGTGAGCTGA[-/G]TTTGCGCCATTGCAC | 92912 |
rs201809996 | in-del | -/TCT | 0.0123036 | 0.0774623 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75845089 | GCTCTCAGAACTCAG[-/TCT]TCTTGGGGGAAGAGT | 92912 |
rs202076371 | snp | A/G | 0.000696633 | 0.0186502 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883353 | TAATTAAACTTGCTT[A/G]TTTGCTTTTTAGGAT | 92912 |
rs202167888 | in-del | -/GCA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856774 | ATGGCGAAACCCCAT[-/GCA]CTCTACTAAAAATAC | 92912 |
rs202167934 | snp | C/T | 0.00199806 | 0.0315443 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859873 | TACTGAAATGTGTTT[C/T]GTAGCTTCGTCAGCA | 92912 |
rs202184146 | in-del | -/A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891497 | AAGTTTTTTTTTTTT[-/A/T]AAATCTTTTTATTAA | 92912 |
rs202209762 | snp | C/T | 7.4262e-05 | 0.00609307 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843814 | AGCCCGCACTCGCTG[C/T]CGCCGCCACTCACGC | 92912 |
rs202219493 | in-del | -/TG | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865803 | TGAATAATATCTGGT[-/TG]TTTTTTTTTTTTTTA | 92912 |
rs367551866 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75870470 | TTAGCTTAGGTGGAA[G/T]AAACTGCATGAAAAC | 92912 |
rs367556226 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75848108 | ACTGTGTTTCTGTGT[A/G]CTATAGATAATATTT | 92912 |
rs367569213 | in-del | -/TTTCGTT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872898 | TTTCATTTTAAAGTT[-/TTTCGTT]ACAGGAGAAATTAGG | 92912 |
rs367689927 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879068 | TCTCTAACTTTTTAT[C/T]TGAACTGTTTTTTGT | 92912 |
rs367790617 | in-del | -/GTTCGAGACCACCTTGGGCAACATGGTGA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75894362 | GGCCTGAGCTCAGGA[lengthTooLong]AACCAATCTCTGTAA | 92912 |
rs367804767 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871478 | TATCACATGGGGAGA[A/T]ACCTTAGACAATACC | 92912 |
rs367898449 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900472 | AAGGTACTCTCCATT[G/T]TATTGCCTTACCTGA | 92912 |
rs367909408 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75862193 | ACTGTGGGATGGGCC[C/G]ATCCAAGGACGTGAT | 92912 |
rs367912525 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890178 | TCTTAATTACTGATA[C/T]CATACAAATCTGAAA | 92912 |
rs367964778 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75897227 | TTATTTATTTATTTA[-/T]TTTATTTTATTTTAT | 92912 |
rs368032024 | snp | A/T | 5.66685e-05 | 0.00532269 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879235 | TCCAGTGGGGTGCGT[A/T]TATTTGTACAAGTGC | 92912 |
rs368038104 | snp | A/G | 1.65162e-05 | 0.00287365 | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75883389 | TCCATTTGATCCTCC[A/G]TTTGTTCGAGTGGTG | 92912 |
rs368241686 | snp | C/T | 0.00140073 | 0.0264273 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843747 | GCGATTCCGCATCGT[C/T]AGTTGGAAGCTGGAC | 92912 |
rs368429883 | snp | C/G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896234 | AGGAAGGGGGATGAA[C/G/T]GGGAGGAAACTGGGT | 92912 |
rs368456689 | snp | A/G | 1.64928e-05 | 0.00287161 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75868909 | ACTCAGCCTGTGCAT[A/G]TTTGTTCTGTATAGC | 92912 |
rs368559982 | snp | G/T | 0.000248149 | 0.0111361 | synonymous-codon, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75868971 | GACAACAGAAGAAGT[G/T]ACTTCAGAAGAAGAG | 92912 |
rs368645292 | in-del | -/TTCTT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75858999 | TTCTCTTCATCTCTT[-/TTCTT]GGTCAGAGCCACCTA | 92912 |
rs368745488 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75851482 | TCAATATTGCCATCA[A/G]TGTTATCAGGATATT | 92912 |
rs368775710 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863435 | TTTTCCTTCTGTTTT[G/T]TTTGTTTGTTTGTTT | 92912 |
rs368861921 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889127 | CTCTTTTAGCCCAGT[A/G]GGAGAGTTAAAGAGT | 92912 |
rs368886309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75859507 | GGGTTATTTTTTCTG[C/T]TATTTTTTGTTTTTA | 92912 |
rs368980638 | snp | A/G | 0.000704402 | 0.0187538 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873416 | AAGCTAACATTTTTC[A/G]TCTCTTTGTAGGATA | 92912 |
rs369094609 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75846155 | GTACTCCACTTTAGA[C/T]TATTTTGAAGCAGAT | 92912 |
rs369094958 | snp | A/G | 1.64836e-05 | 0.0028708 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876165 | CAGCAGACCCTGGTA[A/G]ACAGTGGCTTTTGTG | 92912 |
rs369281797 | snp | C/T | 1.65007e-05 | 0.00287229 | utr-variant-3-prime, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75899462 | GAAGATGGCTAAATG[C/T]GTTGACTGTTGTATG | 92912 |
rs369325060 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75844243 | GTTTGAGCCCAGGCC[A/G]GCAAGGGGAACGGCC | 92912 |
rs369416295 | snp | A/G | 3.34342e-05 | 0.00408852 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75890498 | GGTGACTTTTCTTAC[A/G]ATACTCCATTTTCAC | 92912 |
rs369513492 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75852716 | CTGAAGAATTTGAAG[A/G]AGAAAATGCAGTACT | 92912 |
rs369632229 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75863974 | AGACATCTGCAGCTT[G/T]TGTTTTTCACTGAAT | 92912 |
rs369665455 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885585 | GGACGGTGTCCTCTG[A/G]CTTACTCTCTGGGAA | 92912 |
rs369673866 | snp | A/G | 0.000120391 | 0.00775765 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75899380 | ATGCCAGTTCTTCTA[A/G]TTTATTTAAGAATTA | 92912 |
rs369700763 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895103 | AAGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 92912 |
rs369728309 | snp | G/T | 3.30464e-05 | 0.00406474 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859896 | CGTCAGCAATTGAAG[G/T]GGTTGATATGTGAAC | 92912 |
rs369731482 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75900572 | CTTAAGCACTTTTAA[C/G]AAATCCAGAAGCACA | 92912 |
rs369747256 | in-del | -/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75879750 | CCATGGAGCAGGGGG[-/G]TAAAACTAGGAAGAA | 92912 |
rs369755727 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75872527 | CAAATTCTTTGTTTT[C/T]TTTTCCTTTTTTTTT | 92912 |
rs369776713 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75885790 | TGTGAAATAGTTGTT[A/T]AGAATTGTGTACAGT | 92912 |
rs369813136 | snp | A/C | 0.000168996 | 0.00919073 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75896952 | ATTGTAATAATTTTC[A/C]CCTAATTACACTTTT | 92912 |
rs369848940 | snp | C/G | 1.70563e-05 | 0.00292025 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75873604 | AGAACCTGGACTTTT[C/G]TGGTTAAATAATTGT | 92912 |
rs369893138 | snp | C/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75874539 | TCCACCTGCCTTGGC[C/T]TCCCGAAGTGCTGGG | 92912 |
rs369975950 | in-del | -/AA | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75875727 | TTAATATCCTCTTGA[-/AA]CTTCATAATGCTTCA | 92912 |
rs370086387 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865890 | TCTGTTATTTGTTCA[A/G]CAAATATCTGACTCT | 92912 |
rs370189924 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876543 | TCTTACATGATTTTT[A/G]TCTTCTGGGGAAAGC | 92912 |
rs370196862 | snp | A/G | | | upstream-variant-2KB | UBE2Q2 | GRCh38.p7 | 15:75842104 | ACTCTAGGTAAGACT[A/G]GAAAAGGAAAATGCG | 92912 |
rs370222389 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75895369 | TGGTATTTTTGTAGA[G/T]ACGGGGTTTCTCCGT | 92912 |
rs370354128 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887239 | TATCAAATGCTAACC[A/G]TGGACTTAATTTATC | 92912 |
rs370400671 | snp | G/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75854756 | AAACAAGCATTTTGG[G/T]TAGAGACCACTAGCC | 92912 |
rs370490637 | snp | C/G | 4.14697e-05 | 0.00455336 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843787 | TGCCAGTTCCTGGTG[C/G]CGCAGCAGGGCAGCC | 92912 |
rs370510765 | snp | G/T | 1.65803e-05 | 0.00287922 | stop-gained, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75877998 | AAATGACAGTTTATA[G/T]GACTGGCATGTTAAA | 92912 |
rs370564605 | snp | A/C | 0.000265463 | 0.0115179 | missense, intron-variant, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75859972 | TAGATCAACCACTAC[A/C]CACGGGTCAGGTAAA | 92912 |
rs370603415 | snp | C/G | 0.000153988 | 0.00877327 | upstream-variant-2KB, missense, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75843702 | GGCCGAGCTGAAGTT[C/G]CTGGCGTCCATCTTC | 92912 |
rs370614277 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75865230 | TTACCACTTATGTAT[A/G]CATCCTTGAACAATA | 92912 |
rs370675208 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2Q2 | GRCh38.p7 | 15:75901044 | AAGAACCATTTAAAA[A/T]TTTTGTTTGTGCTGA | 92912 |
rs370680072 | snp | C/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75871515 | TCCTAGGCAGAGGTC[C/G]CTGCGGCCTTCCGCA | 92912 |
rs370683535 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75883667 | AGAGCTAGTCCCAGG[A/G]TTTCTGATTCAGTAG | 92912 |
rs370732333 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75876750 | CCTTGTTTGACGAGT[A/G]TTCTTACTCAATATG | 92912 |
rs370761917 | snp | A/G | 0.000159987 | 0.00894249 | upstream-variant-2KB, intron-variant | UBE2Q2 | GRCh38.p7 | 15:75843858 | CACGGTGAGGCGCCC[A/G]GCCGCGGCCCCGCGG | 92912 |
rs370790948 | snp | A/T | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75891877 | AGCTTCCATTCACTA[A/T]GGAGGGAATGGTAGT | 92912 |
rs370829347 | in-del | -/A | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75889188 | AATACACAAAAAAAA[-/A]TTTAATCCCATGAAC | 92912 |
rs370916357 | snp | A/G | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75887042 | TTTAAAATCTGTTAC[A/G]TAGTTTCTTAATTGA | 92912 |
rs370925975 | in-del | -/GT/GTGTGTGT | | | intron-variant | UBE2Q2 | GRCh38.p7 | 15:75856246 | TATATGTGTATATAC[-/GT/GTGTGTGT]GTGTGTGTGTGTGTG | 92912 |