SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs471862 | snp | A/C | 0 | 0 | intron-variant | UBE2N | GRCh38.p7 | 12:93425978 | TTCAGATTCTTCCCA[A/C]AACCTTGAGGTAGGG | 7334 |
rs486398 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2N | GRCh38.p7 | 12:93423173 | GCACACAGTGTGAGC[A/G]CTGAAATCATCGTGA | 7334 |
rs494999 | snp | A/T | 0 | 0 | intron-variant | UBE2N | GRCh38.p7 | 12:93425764 | AGCTAAGGCTTTTGG[A/T]CAGACGTGTGAAATA | 7334 |
rs506911 | snp | A/G | 0 | 0 | intron-variant | UBE2N | GRCh38.p7 | 12:93413665 | ttgccaatcaggcta[A/G]atgtgtgtggcatat | 7334 |
rs531209 | snp | A/C | 0 | 0 | intron-variant | UBE2N | GRCh38.p7 | 12:93432187 | cagtgagccaagtca[A/C]gtcactgcattccag | 7334 |
rs535319 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2N | GRCh38.p7 | 12:93442957 | CAGGTCTTGGCGGAT[C/T]TGCCTGGGGACAAAA | 7334 |
rs558419 | snp | A/T | 0 | 0 | intron-variant | UBE2N | GRCh38.p7 | 12:93415463 | TTGAACCTAAAGATC[A/T]TGTCAGTTTCTCACT | 7334 |
rs563933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2N | GRCh38.p7 | 12:93410413 | TAAACAGCTGAATAC[C/T]TTAATCAAATGGGTT | 7334 |
rs563965 | snp | A/T | 0 | 0 | intron-variant | UBE2N | GRCh38.p7 | 12:93410422 | GAATACTTTAATCAA[A/T]TGGGTTACAAAAACA | 7334 |
rs574299 | snp | A/T | | | utr-variant-3-prime | UBE2N | GRCh38.p7 | 12:93409391 | AAAACTTCCGGTAAA[A/T]CTTATGttttaataa | 7334 |
rs596795 | snp | A/G | 0 | 0 | intron-variant | UBE2N | GRCh38.p7 | 12:93427808 | ATCGGTAAGATTCCA[A/G]AATCTCACTGAATAT | 7334 |
rs607605 | snp | A/G | 0 | 0 | intron-variant | UBE2N | GRCh38.p7 | 12:93427675 | tcacaaagtagtaca[A/G]catcatcacttgcta | 7334 |
rs607963 | snp | G/T | 0 | 0 | intron-variant | UBE2N | GRCh38.p7 | 12:93427648 | gctaattccagaaga[G/T]ttttgtcaccccaaa | 7334 |
rs641414 | snp | A/T | 0 | 0 | intron-variant | UBE2N | GRCh38.p7 | 12:93425920 | CGTGATTATTGAGGC[A/T]ATGATCACTTTTTTA | 7334 |
rs643247 | snp | A/T | 0.286678 | 0.247295 | utr-variant-3-prime | UBE2N | GRCh38.p7 | 12:93409372 | TAGAATAACAAAAAA[A/T]ATTTTACTAAAACAT | 7334 |
rs643258 | snp | C/T | 0 | 0 | utr-variant-3-prime | UBE2N | GRCh38.p7 | 12:93409379 | ACAAAAAATATTTTA[C/T]TAAAACATAAGATTT | 7334 |
rs643636 | snp | A/T | 0 | 0 | utr-variant-3-prime | UBE2N | GRCh38.p7 | 12:93409418 | TTCCAGACAAGCCAT[A/T]CAAAATGGTCACAAG | 7334 |
rs657971 | snp | A/T | 0 | 0 | intron-variant | UBE2N | GRCh38.p7 | 12:93413472 | aggcacgatgagggg[A/T]gaggtctgggctaga | 7334 |
rs664063 | snp | A/T | | | intron-variant | UBE2N | GRCh38.p7 | 12:93415465 | TGAGAAACTGACATG[A/T]TCTTTAGGTTCAAAC | 7334 |
rs853669 | snp | G/T | 0 | 0 | intron-variant | UBE2N | GRCh38.p7 | 12:93432475 | GTTTTTTTTTTTTTG[G/T]GACTCTTAAAGACAA | 7334 |
rs1021136 | snp | A/G | 0.231189 | 0.249291 | intron-variant | UBE2N | GRCh38.p7 | 12:93420158 | TCTAAAGTACTCTGA[A/G]ATTTAGTCTTTGGTA | 7334 |
rs1483003 | snp | A/G | 0.499187 | 0.0201513 | intron-variant | UBE2N | GRCh38.p7 | 12:93440603 | ATTCTTGTGAAATCT[A/G]TGGGGAGATGCATAC | 7334 |
rs1803750 | snp | C/T | | | utr-variant-3-prime | UBE2N | GRCh38.p7 | 12:93409571 | TCTTTAGAATATGCT[C/T]TAGCCAAGTCTAACT | 7334 |
rs1845371 | snp | A/C/G/T | 0.526538 | 0.080326 | intron-variant | UBE2N | GRCh38.p7 | 12:93421216 | AGAATCTGTCCCCCC[A/C/G/T]GCCCCCCCAAAAAAA | 7334 |
rs2291266 | snp | A/C | 0.231775 | 0.249335 | intron-variant | UBE2N | GRCh38.p7 | 12:93426357 | TTCTTGCTAGCAACA[A/C]GAGCCAGCAATGTTA | 7334 |
rs3049603 | in-del | -/GTA | 0.0130921 | 0.0798413 | intron-variant | UBE2N | GRCh38.p7 | 12:93439889 | GAAACTAAGACAGTA[-/GTA]ACTCATACTGTGATA | 7334 |
rs3759169 | snp | C/T | 0.23846 | 0.249734 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2N | GRCh38.p7 | 12:93443324 | AGAGAGAAAAAATAG[C/T]GCACTAAAGAAACTG | 7334 |
rs3782416 | snp | A/G | 0 | 0 | intron-variant | UBE2N | GRCh38.p7 | 12:93433795 | CATCCATAGTTCATT[A/G]TAACAGAAAACATAA | 7334 |
rs3882947 | snp | C/T | 0.499885 | 0.00758699 | upstream-variant-2KB | UBE2N | GRCh38.p7 | 12:93444695 | gattacaggtgtgag[C/T]cactccacctggccT | 7334 |
rs3952508 | snp | A/C | 0.183886 | 0.241099 | upstream-variant-2KB | UBE2N | GRCh38.p7 | 12:93444209 | ttttttaaaacaaaa[A/C]aaaacaaaacaaaaa | 7334 |
rs4020452 | in-del | -/TTTTT/TTTTTT | | | intron-variant | UBE2N | GRCh38.p7 | 12:93416857 | ttttttttttttttt[-/TTTTT/TTTTTT]nnnnggtagtgatgg | 7334 |
rs4020453 | snp | A/G | 0.26078 | 0.249767 | intron-variant, downstream-variant-500B | UBE2N | GRCh38.p7 | 12:93414158 | CCAGACTTTTTTTGA[A/G]ATGGAGTCTCGCCCT | 7334 |
rs4020454 | snp | C/T | 0.172028 | 0.23753 | intron-variant, nc-transcript-variant | UBE2N | GRCh38.p7 | 12:93413101 | TAACAAACAAGTTAG[C/T]GATAACTACAGCTTG | 7334 |
rs6538418 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | UBE2N | GRCh38.p7 | 12:93435417 | ggcagaggttgcagt[G/T]agccgagatcacgcc | 7334 |
rs7132349 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | UBE2N | GRCh38.p7 | 12:93441482 | CCCGAGCCCCGCCGC[A/G]ATTcccgcgcgcccg | 7334 |
rs7295360 | snp | A/G | 0.170408 | 0.236992 | intron-variant | UBE2N | GRCh38.p7 | 12:93436187 | gctcactgcagcctc[A/G]acttcctgggccaaa | 7334 |
rs7295796 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | UBE2N | GRCh38.p7 | 12:93436285 | tcattttatcttttt[C/G]tagagacaaggtctc | 7334 |
rs7299705 | snp | A/C | 0.1652 | 0.235179 | intron-variant | UBE2N | GRCh38.p7 | 12:93437269 | cacctgatattagga[A/C]ttcgaggctgtatgt | 7334 |
rs7300607 | snp | C/T | 0.492533 | 0.0606443 | intron-variant | UBE2N | GRCh38.p7 | 12:93437870 | ATGAGGGATTCTCTA[C/T]GTATCCTTCAGAGCC | 7334 |
rs7303001 | snp | G/T | 0.0810805 | 0.184299 | intron-variant | UBE2N | GRCh38.p7 | 12:93434230 | ctgggaggtggagat[G/T]gcagttagccgagtt | 7334 |
rs7303274 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | UBE2N | GRCh38.p7 | 12:93415851 | GCTACAGAAAGGCCT[C/T]CAAAAGCGTATCCCA | 7334 |
rs7303325 | snp | A/G | 0.1652 | 0.235179 | intron-variant | UBE2N | GRCh38.p7 | 12:93416004 | CATGTGACCTGATCA[A/G]GCCTAGATTTAATTG | 7334 |
rs7305153 | snp | A/G | 0.231482 | 0.249313 | intron-variant | UBE2N | GRCh38.p7 | 12:93433078 | gctgggactacaggc[A/G]cccaccaccacgccc | 7334 |
rs7305670 | snp | A/C | 0.231482 | 0.249313 | intron-variant | UBE2N | GRCh38.p7 | 12:93433468 | GATTCCCTATTATTT[A/C]ATTGCCTAATTGGTA | 7334 |
rs7309933 | snp | C/T | 0.121717 | 0.214577 | intron-variant | UBE2N | GRCh38.p7 | 12:93420470 | CTAAAAGTTTCTCCC[C/T]TGTACTTCCAGTTTC | 7334 |
rs7311222 | snp | A/G | 0.499859 | 0.0083854 | intron-variant | UBE2N | GRCh38.p7 | 12:93417496 | CAGTATTCTTAGAAA[A/G]AGTGCTAATTTGTGT | 7334 |
rs7314146 | snp | A/G | 0.136506 | 0.222754 | intron-variant | UBE2N | GRCh38.p7 | 12:93428180 | ttgcttcagcctccc[A/G]aagtgctgggatcac | 7334 |
rs7342330 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2N | GRCh38.p7 | 12:93443808 | gctgttagtttcact[C/T]caagtgggcctctcc | 7334 |
rs7484824 | snp | A/C | 0.499859 | 0.0083854 | intron-variant | UBE2N | GRCh38.p7 | 12:93419555 | CAAACAAGCTAACTG[A/C]ATGATGAAGTAAAGA | 7334 |
rs7484825 | snp | A/G | 0.183568 | 0.241012 | intron-variant | UBE2N | GRCh38.p7 | 12:93419556 | AAACAAGCTAACTGA[A/G]TGATGAAGTAAAGAG | 7334 |
rs7953247 | snp | A/C | 0.165527 | 0.235296 | intron-variant | UBE2N | GRCh38.p7 | 12:93434429 | CTTGATAATTTGACA[A/C]AACTTAATTTCACTT | 7334 |
rs7957305 | snp | A/G | 0.0788843 | 0.182262 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2N | GRCh38.p7 | 12:93442422 | CAGTGAACGACTGAG[A/G]TGGGGCTCATCGTCT | 7334 |
rs7969431 | snp | A/G | 0.0284514 | 0.115828 | intron-variant | UBE2N | GRCh38.p7 | 12:93410717 | AAGTGGTGTGAAGGA[A/G]AATGAATATTAGATA | 7334 |
rs7972279 | snp | A/T | 0.0788843 | 0.182262 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE2N | GRCh38.p7 | 12:93442601 | GCTGAAGGAAAAGGG[A/T]TTGGAGCGAGTTGGA | 7334 |
rs10437876 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | UBE2N | GRCh38.p7 | 12:93430171 | cctttcctattttga[A/T]acacacatacttacc | 7334 |
rs10459180 | snp | C/T | 0.23846 | 0.249734 | intron-variant | UBE2N | GRCh38.p7 | 12:93441305 | GGCAGGACGCGCGGG[C/T]CTCCCAGAGCCACTT | 7334 |
rs10459181 | snp | C/G | 0.2339 | 0.25045 | intron-variant | UBE2N | GRCh38.p7 | 12:93441325 | CAGAGCCACTTCCCG[C/G]GGCGCAGGGCCCCGC | 7334 |
rs10714261 | in-del | -/G | 0.228842 | 0.249103 | intron-variant | UBE2N | GRCh38.p7 | 12:93441509 | CCCGCGGCCTCCGGC[-/G]GGGGGGTGGTCTCAG | 7334 |
rs10859492 | snp | C/T | 0.499885 | 0.00758699 | upstream-variant-2KB | UBE2N | GRCh38.p7 | 12:93445311 | AAAACAGTGGTTACC[C/T]GGAGCAGGTTGTGGG | 7334 |
rs11107016 | snp | C/T | 0 | 0 | utr-variant-3-prime | UBE2N | GRCh38.p7 | 12:93408567 | TGTATTTATGACTGG[C/T]TACATTTATGACTTA | 7334 |
rs11107017 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | UBE2N | GRCh38.p7 | 12:93418425 | ATTTTCAAGTGCATA[C/T]CCCTTGCTTCATTTT | 7334 |
rs11107018 | snp | A/G | 0.183886 | 0.241099 | intron-variant | UBE2N | GRCh38.p7 | 12:93420126 | ACGGAAGAAAAATCT[A/G]TTTCTAAGATTCTGC | 7334 |
rs11107020 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBE2N | GRCh38.p7 | 12:93426508 | GCTGGAACACAGGTA[A/G]GAGACACCCTGCAAG | 7334 |
rs11107021 | snp | A/T | 0.172028 | 0.23753 | intron-variant | UBE2N | GRCh38.p7 | 12:93428120 | ACATGGGGCTTCTTC[A/T]TGTTGCCCAGGCTTT | 7334 |
rs11107022 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | UBE2N | GRCh38.p7 | 12:93428209 | ACAGACATGAGCCAC[C/T]GCACCCAGCCAACAG | 7334 |
rs11107023 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBE2N | GRCh38.p7 | 12:93429061 | cggatcacgaggtca[A/G]gagttcaagatcagc | 7334 |
rs11107024 | snp | A/T | 0.172028 | 0.23753 | intron-variant | UBE2N | GRCh38.p7 | 12:93429888 | TAATACAAAAAAATC[A/T]AAAGTTTAAAAATAT | 7334 |
rs11107025 | snp | A/C | 0.255503 | 0.249939 | intron-variant | UBE2N | GRCh38.p7 | 12:93430621 | TCTGATTAAAAAAAA[A/C]CAAGAAAAGCGGCAG | 7334 |
rs11107026 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | UBE2N | GRCh38.p7 | 12:93434160 | agctgggtgtggtgg[C/T]gcgtgcctgtaattc | 7334 |
rs11107027 | snp | C/T | 0.23846 | 0.249734 | intron-variant | UBE2N | GRCh38.p7 | 12:93439842 | TTCATTAGATAGATG[C/T]TGTCAACAAGATACC | 7334 |
rs11107028 | snp | A/T | 0.18325 | 0.240924 | intron-variant | UBE2N | GRCh38.p7 | 12:93440623 | TTCACAAGAATGAGC[A/T]AGATTAACATACACG | 7334 |
rs11107029 | snp | C/T | | | intron-variant | UBE2N | GRCh38.p7 | 12:93441528 | gggTGGTCTCAGAAG[C/T]TATGGAGGCCCGCGC | 7334 |
rs11107030 | snp | C/T | 0.0325976 | 0.123435 | upstream-variant-2KB | UBE2N | GRCh38.p7 | 12:93444568 | GCGTGTGCCACTGCC[C/T]CCTGCTAATTTTTGT | 7334 |
rs11558873 | snp | A/G | | | utr-variant-5-prime, missense, nc-transcript-variant | UBE2N | GRCh38.p7 | 12:93442152 | TCGCGGCCTGTCCCA[A/G]GTCCCTGCCCCGCAA | 7334 |
rs11558874 | snp | A/G | | | utr-variant-5-prime, missense, nc-transcript-variant | UBE2N | GRCh38.p7 | 12:93442048 | AGCCCGCCCGTGCCC[A/G]AGCCCGCGCCCGAGC | 7334 |
rs11558875 | snp | A/C | | | missense | UBE2N | GRCh38.p7 | 12:93410848 | CCAGCACTGCAGATC[A/C]GCACAGTTCTGCTAT | 7334 |
rs11558876 | snp | C/G/T | 1.64841e-05 | 0.00287085 | missense | UBE2N | GRCh38.p7 | 12:93411193 | GCCCTCAGGATTCCC[C/G/T]CTTTGAGGGAGGGAC | 7334 |
rs11558878 | snp | G/T | | | utr-variant-3-prime | UBE2N | GRCh38.p7 | 12:93408454 | TCTGAAGAAACTCCA[G/T]AATTACGAGAATAAG | 7334 |
rs11831401 | snp | A/G | 0.231482 | 0.249313 | intron-variant | UBE2N | GRCh38.p7 | 12:93432763 | AAGACAACATAGCCA[A/G]TTGTTTTAATGCAAA | 7334 |
rs11833560 | snp | C/T | 0.00943375 | 0.0680285 | intron-variant | UBE2N | GRCh38.p7 | 12:93437388 | aaGTCAACTTGAAGA[C/T]ACATAGGTGGTTAGA | 7334 |
rs11835400 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE2N | GRCh38.p7 | 12:93414060 | cagctactcgggagg[C/T]tgaggcaggagaatc | 7334 |
rs11835441 | snp | C/T | 0.136506 | 0.222754 | intron-variant, downstream-variant-500B | UBE2N | GRCh38.p7 | 12:93414252 | gtcaggagttcgaga[C/T]cagcctgatcaacat | 7334 |
rs11835514 | snp | A/G | 0.0240643 | 0.107019 | intron-variant, downstream-variant-500B | UBE2N | GRCh38.p7 | 12:93414390 | ggaggtggaggttgc[A/G]gtgagccccgatcat | 7334 |
rs12303259 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBE2N | GRCh38.p7 | 12:93415772 | GAAAGCCAGGGCCCA[A/G]GAGTCCCAATCCACC | 7334 |
rs12312856 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | UBE2N | GRCh38.p7 | 12:93439257 | tgtgggaggctgaaa[C/T]gggtggattgtgtga | 7334 |
rs12318501 | snp | A/G | 0.031825 | 0.122064 | upstream-variant-2KB | UBE2N | GRCh38.p7 | 12:93444135 | GAAACTGCCACATGT[A/G]CAATATTTGTCAGAG | 7334 |
rs12426990 | snp | A/C | 0.23846 | 0.249734 | intron-variant | UBE2N | GRCh38.p7 | 12:93417881 | ATTTGTAAGATAAAA[A/C]AAACGGGCTCCTTTT | 7334 |
rs12809242 | snp | A/G | 0.166832 | 0.235761 | intron-variant | UBE2N | GRCh38.p7 | 12:93441034 | TATCTACGAAAAAGA[A/G]AGGAGAGGAGAGAAG | 7334 |
rs12810300 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | UBE2N | GRCh38.p7 | 12:93413948 | gggtggatcacctca[A/G]gtcaggagttcgaga | 7334 |
rs12821477 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | UBE2N | GRCh38.p7 | 12:93420418 | AAAGTATATATAATC[A/T]GAGATACATCAGAAT | 7334 |
rs12821933 | snp | A/T | 0 | 0 | downstream-variant-500B | UBE2N | GRCh38.p7 | 12:93408173 | TTCATTTTTAAAGTG[A/T]GATTCAATTTCCTTA | 7334 |
rs12821957 | snp | A/G/T | 0 | 0 | downstream-variant-500B | UBE2N | GRCh38.p7 | 12:93408221 | CCTTTAAACAGCCCA[A/G/T]GAATTGTTATAAATG | 7334 |
rs12822459 | snp | A/G | 0 | 0 | downstream-variant-500B | UBE2N | GRCh38.p7 | 12:93408222 | CTTTAAACAGCCCAA[A/G]AATTGTTATAAATGA | 7334 |
rs12826404 | snp | C/G | | | intron-variant | UBE2N | GRCh38.p7 | 12:93421215 | ttttttttggggggg[C/G]tggggggacagattc | 7334 |
rs12830302 | snp | C/T | 0.130351 | 0.219509 | intron-variant | UBE2N | GRCh38.p7 | 12:93418250 | tgactatagtcctag[C/T]gtacttgggaggttg | 7334 |
rs17021218 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | UBE2N | GRCh38.p7 | 12:93416017 | CAAGCCTAGATTTAA[C/T]TGGAACACATTCTAA | 7334 |
rs17021220 | snp | C/G | 0.169435 | 0.236663 | intron-variant | UBE2N | GRCh38.p7 | 12:93417083 | ATGTTCAGGAAGTTA[C/G]TTACTAAAATAGACA | 7334 |
rs17021222 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2N | GRCh38.p7 | 12:93420388 | ACTTGGGAGCTGGAG[A/G]GACTTCTGAAAGTCA | 7334 |
rs17021223 | snp | C/T | 0.153332 | 0.230554 | intron-variant | UBE2N | GRCh38.p7 | 12:93420591 | CCAGCTAGTAAATGG[C/T]GGTAAATTCTAAATA | 7334 |
rs17021224 | snp | A/G | 0.230896 | 0.249269 | intron-variant, utr-variant-3-prime | UBE2N | GRCh38.p7 | 12:93424128 | CATTTTTTCACTCCT[A/G]TGTCACTGCAGCCAC | 7334 |