SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs536510900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427111 | GGATGGAGAGAACAG[A/G]ATAAAGAGAGAAAGA | 137886 |
rs536640086 | in-del | -/TTTTTTG | 0.00755907 | 0.0610114 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409553 | GTTTATCAAATGCTT[-/TTTTTTG]TTTTTTGTTTTTTGT | 137886 |
rs536741187 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409907 | TGCCAAAGCTCGGGC[A/G]GCAAGCTGTCGACTC | 137886 |
rs536891788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422290 | GTTAGTGAGAATGGC[A/C]GCCAAACTAACTCAG | 137886 |
rs536899415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426432 | CCAGGATGGTCTCAA[C/T]CTCCTGACTTTGTGA | 137886 |
rs536943553 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422354 | CTACTACCAGGGCTG[A/G]ATCTAGGCCTTCCTT | 137886 |
rs536984392 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450872 | CCACAGGATGAAAGT[-/G]GTGAGCCCACCACTG | 137886 |
rs537004965 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423893 | CGTTTTCCCACCACA[A/G]CCTTCTCAGTCAAAA | 137886 |
rs537032917 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432346 | GCACTCCTTTCTCCA[C/T]TGAATTGCTTTTGTA | 137886 |
rs537034946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440607 | TAAAAGTTACCCTCT[A/G]CTCGTCCACATATTG | 137886 |
rs537171115 | snp | A/C | 3.41752e-05 | 0.00413357 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439798 | AAATGAGAAAAATAC[A/C]TTTGTTGAACATGAA | 137886 |
rs537184812 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426732 | CCGTTCCTTGCTCAG[C/G]CTCCACTGGGCTCGG | 137886 |
rs537226830 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421567 | TTCCAAATAACCTGA[C/G]TCACCCATTACTGAC | 137886 |
rs537318640 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450365 | ATCACTTAAAAGTTC[G/T]GCTTTACACATAACG | 137886 |
rs537369518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426722 | CGTGACAGACCCGTT[C/G]CTTGCTCAGGCTCCA | 137886 |
rs537463786 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449749 | TCTGGGCTTGTTGAC[C/T]GTCTCAGAGTCATCT | 137886 |
rs537487484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417187 | GGAAAAATTACCTTA[A/T]AATACCTAATATTTT | 137886 |
rs537559639 | snp | C/T | 0.0119091 | 0.0762411 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447622 | AGGACAATACTTCAG[C/T]ATTAAAAACAGCCAA | 137886 |
rs537562567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428633 | ATTCCTTTTCACTTA[C/T]ATTTAATAAGTTAGT | 137886 |
rs537821996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416402 | TTTGGTAGACTTTTA[A/G]ATAGAATACTTCTGA | 137886 |
rs537960125 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423306 | CTGCAGGCAGAAAGA[A/G]AAGCCCAGACATCCC | 137886 |
rs538002234 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410646 | CTACAGGCACGCTCC[A/G]CCACGCCCAGCTAAT | 137886 |
rs538093153 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411275 | CGCGGGTTCGGGTAG[C/G]GGGGACGCGCACGCA | 137886 |
rs538143137 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410019 | AAGCAAAGCTCTACT[A/G]CAAGCTGCATCTTAC | 137886 |
rs538232251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429422 | GGGACAAGGGCTTCC[A/G]TAGGCTCCTGCTCTA | 137886 |
rs538474547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419205 | GTATAGCAGATTGTT[C/T]GCAATCTTTTTTTCT | 137886 |
rs538493384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430129 | TCACTAACTAGGTCT[C/G]TACTGAGTGTGGCCT | 137886 |
rs538525473 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412929 | GCTATAACTTTCCCT[A/G]GCTAGTCAATTCTAA | 137886 |
rs538575073 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428799 | AACTGACAGTAGACC[A/C]TGGACCAAAATACGA | 137886 |
rs538759060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427314 | CATCTCTACAAAAAA[A/G]TAGCCAAGCGTGGTG | 137886 |
rs538774464 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412190 | TTGACAAGTAAATAT[C/T]AGTAAGGAGATACTA | 137886 |
rs538810870 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409645 | GCTCACTGCAACCTC[C/T]GCTTCCCGGGTTCAA | 137886 |
rs538834881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424517 | CATAAACTTTCTTGC[G/T]AAAGTTTGATCTTTT | 137886 |
rs538964226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423735 | CCACCGCGCCCAGCC[A/G]GGGATGGGTTTTTTT | 137886 |
rs538981555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429301 | CTTTTCTGTGTTTGT[C/T]GTCGCTCCCTAAAAT | 137886 |
rs538990241 | snp | C/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410256 | CGTCTTTACTAAAAA[C/T]ACAAAAGTTAGCCGG | 137886 |
rs539029131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444487 | ACACTGCTTCCCAGG[C/G]TGATGTAAATGAAAT | 137886 |
rs539148463 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410724 | TGTGTATATATATAT[G/T]TGTGTGTATATATGT | 137886 |
rs539150788 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443216 | CTGACGGGAATTCAC[A/G]TTCTTATTATGTTTC | 137886 |
rs539240748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438086 | GCTGCATCTCCAGCC[A/G]CAGCTCAAAAAGCCC | 137886 |
rs539294558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436290 | GTGGACTTTACTTCC[C/T]GGAGATTTCAAAGTA | 137886 |
rs539308165 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432770 | TTTCATACATTCTTA[A/C]AAGTAGCATTTCTCA | 137886 |
rs539328736 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414868 | CATGGGGCTAGTGGC[A/G]TTTTTGCTTTTTTAA | 137886 |
rs539376930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446270 | GTATTTAAACAGTCT[C/T]TATAAACTATCCAAA | 137886 |
rs539505053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430992 | ATGGTTACGTTTCAC[A/G]TGATTGTAGTATAAT | 137886 |
rs539567086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425362 | CAAAAGTCGTTCACC[A/G]TGTTTTGCAGGCAGC | 137886 |
rs539648437 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447608 | GTGCCGTATTAATAA[G/T]GACAATACTTCAGCA | 137886 |
rs539799306 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450612 | TAGCTTCTTTTCTGG[C/T]ATGCTCCTCAGAATT | 137886 |
rs539860177 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451265 | CATTAGGAGAGAATT[A/G]AACATCCAGGAGGGA | 137886 |
rs539881212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419788 | GAACCAGCAGAACTT[C/T]AGTAGCTTAGTAGCA | 137886 |
rs539905166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416521 | GAACATCTTCAGGAA[C/T]TCTTAAAAGAATTGC | 137886 |
rs539973579 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409715 | CAGGCACGCGCCACC[A/G]CGCCCAGCTAATTTT | 137886 |
rs540055294 | in-del | -/GG | 0.00770914 | 0.0616047 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424688 | GTTGGAGTACAAGGC[-/GG]GGGGGGGGGCTCTGA | 137886 |
rs540140298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412565 | GTAGAATAGTTCCAG[C/G]TCCCATAGTTGGTTC | 137886 |
rs540203005 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58435786 | CACACCATATCTGCA[A/G]TAATGTACAAATTAT | 137886 |
rs540242429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443088 | GCTGAGCAGGCAGTG[C/T]TGTGCCTCGCCAGTC | 137886 |
rs540634672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425048 | CCTGCTTATGGTGCA[C/T]CTCCTCCAGGAAGTC | 137886 |
rs540737444 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437754 | AAGAGAAGCAGAGCC[C/T]GTTGAAGTTTGGAAA | 137886 |
rs540757283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417477 | TGGGTGATGATTCCT[C/T]TAATGTGTGACCTCC | 137886 |
rs540945636 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411337 | CAGGCAACCGGCCCC[A/G]GAAGTTGCGGCAGGT | 137886 |
rs540962702 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419477 | TACAAGAGGAGTTAC[A/G]TAATCTACAGAAAGA | 137886 |
rs541010279 | in-del | -/CTC | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440840 | TTTCTGTATTCTCTT[-/CTC]CTGATAGAGACTGGC | 137886 |
rs541032421 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448461 | TTACAGGCATGAGCC[A/G]CCACGCCCAGCCTAA | 137886 |
rs541154603 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424456 | TTTGCTTATCAAAAG[G/T]TAGTCAACCACAATG | 137886 |
rs541166184 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438247 | CTAGATTTTAGAGGG[C/T]CACGCCAAAGGGAAA | 137886 |
rs541169484 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447875 | AAAACCCCTTTTTGA[C/T]AAATGCATTTGGTAA | 137886 |
rs541326292 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418190 | AAGTTGCAGAGAGCC[A/G]AGATGGCGCGACTGC | 137886 |
rs541328043 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431877 | GCTTCCTTGCCATTA[A/T]CTGTATTATTCTTTT | 137886 |
rs541368954 | snp | C/T | 1.68434e-05 | 0.00290197 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416842 | GTAACAAGCCTGTTA[C/T]TATGTAGTTGGCCTT | 137886 |
rs541387339 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428657 | AGTTAGTTTGAATGA[G/T]TATAGAGAATTACTT | 137886 |
rs541539577 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422986 | TCCCAATTAACTGCA[C/G]CTCTACTTCACACCC | 137886 |
rs541605343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426567 | ACAAAAAGTGTGAAG[G/T]CTCCAGGGTTACTTT | 137886 |
rs541621208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425493 | GTTGGGATCACCATC[A/G]TGTAGGACAACCCTG | 137886 |
rs541820965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437484 | AGGTGCTCACCACCA[C/T]GCCTGGCTAATTTTT | 137886 |
rs541853981 | in-del | -/TAT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58439916 | AATATTATATCATAA[-/TAT]TATATCATGTGATAC | 137886 |
rs541879351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447024 | GGCTAATCTTGAACT[C/T]CTGGCCTCAAGTGAT | 137886 |
rs541978706 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418090 | TCCTAAAAATACAGA[A/T]ATTAGCTGGGCATGG | 137886 |
rs542025607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438481 | CAATATGCCCTGTAT[A/G]TGGGACGTGGCATCA | 137886 |
rs542200405 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420386 | GACTACATAATGTAA[A/G]TGGGCAAAAAGGCAA | 137886 |
rs542303140 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58411415 | AGGCCCTGAGCCCGG[C/T]GAGCAGGAGAGGAGG | 137886 |
rs542360914 | in-del | -/TT | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450048 | TATCTTCAAAGAGTC[-/TT]GTGTGTGACCTGATA | 137886 |
rs542383757 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422437 | TGCCACAGCATTTTA[C/T]TACCATCACAAAAGT | 137886 |
rs542390479 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420238 | CTTTTACTCTGATAA[C/T]ACAGCTTTGCAACTA | 137886 |
rs542454368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431831 | TTAATTTGCATTTTC[G/T]TAATAGCTAGTGATG | 137886 |
rs542557798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439067 | GATATGCTGGGTCCC[C/G]TTTTGCCTTCCACTG | 137886 |
rs542578677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414356 | CATTTATTACAGCGT[A/C]TAGAATTGGTTACTC | 137886 |
rs542618990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426945 | TTGGCAAGTTATTTA[A/G]ACTCCTTCAGTCTTA | 137886 |
rs542663241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433952 | TTAGACATTGATAGT[G/T]TCTTGGAAGGTCACT | 137886 |
rs542798562 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448667 | CTCCAGAACAAGACT[A/G]GTGTAGAAATACAGG | 137886 |
rs542800211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441681 | ACTCATGAAAATAAC[A/G]ATATTATCTGATGAT | 137886 |
rs542859968 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449416 | GCATCAACTCTAAAT[C/T]CAAAATCTTATCTGA | 137886 |
rs542864659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413760 | TACAAACTGCAGACT[C/T]GGAAATGTTTTTTTG | 137886 |
rs543089988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440962 | GAAATTTTCTCCCTC[A/G]TCTCTCTTTACACGT | 137886 |
rs543178362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425585 | CCTCTTTTCGGCCGT[A/G]GAGAAGTATGCACTC | 137886 |
rs543185320 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448340 | CACCATGCCTGGCTA[A/G]TTTTTGTACTTTTGC | 137886 |
rs543205293 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415758 | TACGATTTGAATTCA[C/G]TCCTTTTAGATTACC | 137886 |
rs543225335 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418320 | GTAGTCACATATCTC[C/T]TATAGCTTTTTCTTT | 137886 |
rs543330006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412938 | TTCCCTGGCTAGTCA[A/G]TTCTAATATCATTAA | 137886 |
rs543373108 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425075 | AGTCCAGCACACCCC[-/T]GGGGTCAATGGGCAC | 137886 |
rs543413631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440859 | TGATAGAGACTGGCA[C/T]TGGGGACATAAAGGA | 137886 |
rs543413717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432591 | GTTTCACCATGTTAG[A/C]CAGGGTGGTCTCGAT | 137886 |
rs543418717 | in-del | -/AA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58433612 | GACCCTATCTCTTTA[-/AA]AAAAAAAAAAAAAAA | 137886 |
rs543464448 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423432 | GGGGTGGGTTTTTTT[G/T]TTGTTGTTGTTTTTT | 137886 |
rs543505247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431126 | CCCACCCCGTCTCTC[A/G]TGCCATCCCTAACCT | 137886 |
rs543521271 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422471 | TTAATGATATTTTCA[C/T]TGAAATATCCACACT | 137886 |
rs543548670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440338 | CTTGCAGCAGGAGCA[A/G]TGTGCTTAGCTTTGT | 137886 |
rs543735557 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419847 | CAGGAAGGCTTTCAT[A/G]GGCATGTGACCTGTG | 137886 |
rs543923397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422508 | TTCAACATATAAGGC[A/G]AAGAGGGATGTCTTT | 137886 |
rs544209657 | snp | C/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450131 | TCTTCATCACTTTCT[C/G]TAGAGTAAAGGCTGT | 137886 |
rs544229839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442897 | AAAGATTGTGCTTGC[C/T]ACTCTCACTTACCTG | 137886 |
rs544271155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423878 | AGAAAATATGGCAAA[C/T]GTTTTCCCACCACAA | 137886 |
rs544278489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414734 | CTCCCTCTAAATATT[A/G]CTCATTTTCTTCTAA | 137886 |
rs544341796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415628 | TTGTGCTTTCCATAC[A/G]TTATTTAATCCTTCA | 137886 |
rs544378886 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410827 | GGGTTTCACCATGTT[A/G]GCCAGGATGGTCTCG | 137886 |
rs544408955 | snp | A/G | | | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430652 | GCCACAAGAGCTTCA[A/G]GTGATGATAAATCTA | 137886 |
rs544520535 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410250 | AAACCCCGTCTTTAC[G/T]AAAAATACAAAAGTT | 137886 |
rs544533199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417416 | TGCAGGTCTTTTGTC[C/G]TCCATTTAAGAATCT | 137886 |
rs544615284 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411187 | CAAAACTTAACAGAG[A/G]TTTCCCTGCGGAGAA | 137886 |
rs544691568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428153 | AGATTCAGTAGCACA[A/G]TGGGAGCAAAAATCT | 137886 |
rs544726178 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423540 | TCCTGGGTTCACACC[A/G]TTCTCCTGCCTCAGC | 137886 |
rs544731790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426825 | TGTGCACAGACCCCC[C/T]TCCAGGCCTGGGGAT | 137886 |
rs544744845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428855 | ATTTATGACAGTGCA[G/T]AGCAGTGAGGGGCAG | 137886 |
rs545059819 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438250 | GATTTTAGAGGGCCA[C/T]GCCAAAGGGAAATGT | 137886 |
rs545077521 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420944 | GGAGGCCATGTGCTT[A/C/G]CTATATGTAAAACTT | 137886 |
rs545090502 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447685 | GTTTTATTGTTATTC[A/T]GTCTTCCAATCTGAA | 137886 |
rs545173321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417384 | GTGTGTTTCTTGAAG[C/T]CACTCCATGGAGCCT | 137886 |
rs545200527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBXN2B | GRCh38.p7 | 8:58434955 | TTTCAAAAGGTTAGT[C/T]TGAAGTTATAATTTG | 137886 |
rs545308365 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449475 | CACATTGAAGCCATC[C/T]AAATTAAGTTTGGGA | 137886 |
rs545317635 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410188 | GGGAGGCCGAGGTGG[A/G]CAGATCATGAGGTCA | 137886 |
rs545362368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441139 | GACTATAGGCACTGC[C/T]GAGCGCAGCTCATTT | 137886 |
rs545368199 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449983 | AAATCCTGTCTCTGT[G/T]TTTGGCTTTTTCTGA | 137886 |
rs545450981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434221 | ACATGTGGTTTCATT[A/G]ATGTCTTTCACTATG | 137886 |
rs545453791 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436996 | AGATACATGAAGATG[C/T]GGAAGCATCTTTGGA | 137886 |
rs545515842 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427375 | GGCTGAAGTGGCAGG[A/G]TAGCTTGAGTCCAAG | 137886 |
rs545565466 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451388 | TAATCATCTCAAAAA[A/T]GATGTCACAATGAAC | 137886 |
rs545614557 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413418 | ATGTTCTTCCCAAAT[A/G]GTACCTTGGATATTG | 137886 |
rs545657868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436582 | ATGTTGAAATGTGAC[C/T]TCCACTGTTGGGGGT | 137886 |
rs545673743 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424696 | ACAAGGCGGGGGGGG[C/G]GGCTCTGATCTCCAC | 137886 |
rs545767595 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419901 | AGAAGGGCCCTGTGC[G/T]TGGAGTAATGCTTTG | 137886 |
rs545794072 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433785 | TTTAAGATAAAAAAA[C/T]CAATTAAAAAAAGAA | 137886 |
rs545808835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429698 | CAGATATCATTTCCC[C/G]CCATTGTTTTGTTCT | 137886 |
rs545873879 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58415828 | TGTACAAATATGAAT[C/G]TTACTGAATGTGGGA | 137886 |
rs545971279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430194 | CACTGCTTTTCCTTC[C/T]ACATCAGAAGTGCTG | 137886 |
rs546042788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429040 | CTTTATGACCTTAGA[A/G]TAGGCAAAGATTTCA | 137886 |
rs546150627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416789 | TCTATACATAACTTC[C/T]AGTTGTATGGAAGAG | 137886 |
rs546188938 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428503 | TTTCCTCCTGTGTTC[C/G]TCTTCATTCCTAGAA | 137886 |
rs546257867 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411768 | TCGGTTCACGGGTTG[A/G]TGCTTCCTTCTTGAG | 137886 |
rs546333488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418734 | GCAGTTTGGTATCTT[A/G]ACACTAGTTGAACAT | 137886 |
rs546333578 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411090 | CAGAGGATGTTTTCA[C/T]TGTTGAGCTAAATGA | 137886 |
rs546514644 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446741 | TCTGGGTCATATGCT[G/T]CTAACACATTTTATA | 137886 |
rs546783290 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416078 | AAAACAAAAAAAAAA[A/C]CCGGAGATTATGGTC | 137886 |
rs546816618 | snp | A/T | | | intron-variant, utr-variant-3-prime | UBXN2B | GRCh38.p7 | 8:58435066 | GGAATCAAGTGATTT[A/T]GCTATGATAATAAAA | 137886 |
rs546825595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423650 | CCGTGTTAACCAGGA[C/T]GGTCTCGATCTCCTG | 137886 |
rs546962601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423000 | ACCTCTACTTCACAC[C/T]CTTTTTTAAAATCTG | 137886 |
rs546973172 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410320 | CGGGAGGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 137886 |
rs546974801 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450973 | AAAACAACTTGGATA[A/G]TGTGTAACAGCCAGC | 137886 |
rs547022687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436270 | TCACTTTACATGGTC[A/G]TAAAGTGGACTTTAC | 137886 |
rs547036676 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451705 | AAAGGTTCAGGTGCT[G/T]CTTTTTTGCCACAAT | 137886 |
rs547118495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424731 | CTGGTCCGCTAGAGA[A/G]TACTTAATATTTGTA | 137886 |
rs547206106 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446209 | TTTTTGACAGAAGAA[A/T]CATTTTTAAAAGGAC | 137886 |
rs547295534 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444389 | TCAGGCACAATAAGG[C/G]TAAGTGACTTGCCTG | 137886 |
rs547328227 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411185 | CACAAAACTTAACAG[A/T]GGTTTCCCTGCGGAG | 137886 |
rs547350661 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420662 | GGTCACAAATAAACA[A/G]ACAAATTATTAATTA | 137886 |
rs547464567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447089 | CAGGCGTAAGCCACC[A/G]TGCCCAGCTGGACCT | 137886 |
rs547552339 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437959 | AAGGCAGCCCCCCCC[C/G]CAACCCCCATCACAG | 137886 |
rs547619067 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412143 | TCATTTTAGGCGTTT[A/T]TGTGTCTCATTATAA | 137886 |
rs547663752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412429 | CTTCGGAGAAATAGG[A/G]TATGAATACTTAGCA | 137886 |
rs547704790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411480 | TGCAGGTGAGGCGAG[G/T]AGCCGGGGGAGGGAG | 137886 |
rs547723881 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445665 | TTCTAAATAAAACTG[G/T]TTTGCTAAACAGTGA | 137886 |
rs547775207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431309 | GAAACTACAGTGTTA[C/T]ACAAATGGAGTCATA | 137886 |
rs547867004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436118 | GTACCTCTGTGCAGT[C/G]TAGCACTTCCTATGT | 137886 |
rs547867305 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428659 | TTAGTTTGAATGAGT[A/C]TAGAGAATTACTTCA | 137886 |
rs547999902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420352 | TTAATGTCATTTTTT[A/T]AAAAAACAGTTGCAA | 137886 |
rs548139185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426276 | CAGTGGCATGATCTC[A/G]GCTCACTGTAAGCTC | 137886 |
rs548234647 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411837 | GTAGACAGTCACCTG[A/G]ACAGTAATGATACGT | 137886 |
rs548248232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437046 | TTGGAAGACTTTGGA[C/T]GTCCTTGAAGAAGAT | 137886 |
rs548305296 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418578 | TCGGGTATGCTAGAT[A/T]AGTGATATTGTCTGC | 137886 |
rs548388439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445440 | TGGCACCCGTTGAAA[C/G]ACTGTGTTCTAGGCA | 137886 |
rs548394864 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58447028 | AATCTTGAACTCCTG[C/G]CCTCAAGTGATCTGC | 137886 |
rs548399407 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411134 | TGCTGCCCTCTAGGG[C/T]GGCCTACAGTGCCTT | 137886 |
rs548438918 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424712 | GGCTCTGATCTCCAC[A/T]CGTCTGGTCCGCTAG | 137886 |
rs548496997 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418198 | GAGAGCCGAGATGGC[A/G]CGACTGCACTCCAGC | 137886 |
rs548504478 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423522 | CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACA | 137886 |
rs548513976 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438812 | ACATGAGATTTGGGG[A/G]GCCAGTGGTGGAATG | 137886 |
rs548534636 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410670 | AGCTAATTTTTGTGT[A/G]TATATATATATATAT | 137886 |
rs548568416 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431958 | TTACTGTTGAGTTTT[G/T]AGAATTCTTTGTATA | 137886 |
rs548584951 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427614 | AAAGAGGGAAGACTT[-/A]AAATGTTTTAAATTT | 137886 |
rs548669163 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436167 | AACAGAAAAATGAAG[C/T]ATATGAGGTTGTCAG | 137886 |
rs548742007 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417555 | AACTGTGAAGACTTA[A/G]GAGATGAGAACCAGG | 137886 |
rs548807284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425639 | CTTCCGAAAAGCCTT[A/G]TTTGACTTTATTGTG | 137886 |
rs548882800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430927 | AAAAAGAATACAGGG[A/G]GGTTTCATGTACCTT | 137886 |
rs548911645 | in-del | -/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448980 | AGGAGAATCATTTCC[-/T]TGTCATTCCACCTTC | 137886 |
rs548943781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425241 | GATGCCATATTCTTT[C/T]AGAGCATACTCATCA | 137886 |
rs549036949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419710 | GATAAGCACAGAAGA[C/T]AAGGGACAAAATTCC | 137886 |
rs549048626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426355 | GGGACTACAGGTGCC[C/T]GCCACCATGCCCGGC | 137886 |
rs549094448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412333 | ATAAGGACATCAAAT[A/C]CTTAGTCGGTGCTGA | 137886 |
rs549117231 | snp | C/G/T | 5.03663e-05 | 0.00501807 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439616 | TAATGATAACTTTTT[C/G/T]CCCCCCTTTTTAAAA | 137886 |
rs549185410 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449636 | AAGCAGAAACAGATG[A/G]AAAAAGGAGCCATCA | 137886 |
rs549194058 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432624 | CCTGACCTCGTGATC[C/T]GCCTGCCTCGGCCTC | 137886 |
rs549432125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418510 | TGTCTTATAAAATGT[C/G]TAACATTGTAGATCA | 137886 |
rs549449071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414842 | CTTTTCTTAATGTAT[A/G]TTCCACATTCCATGG | 137886 |
rs549495438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419158 | TATATAGGTTGAGAC[A/G]TAAACTGTGTTTAAT | 137886 |
rs549566216 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423458 | TTTTTTTTTTTGACA[C/T]GGAGTCTTGCACTGT | 137886 |
rs549614761 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428372 | AATGAGATTAGAAAA[A/G]CAAAAGTATACAAAT | 137886 |
rs549812093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425160 | CCCTTGCCCAACCTT[G/T]GAAAGTTTAAGTTCT | 137886 |
rs549847836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431475 | ACCATTCATTTATTG[A/G]GGGATATTTTAGTTG | 137886 |
rs549910926 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431902 | TCTTTTCAAGGAAAT[A/G]TCTCTTCATTACTTT | 137886 |
rs550054797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425811 | TCAAAGAATCATACC[A/G]TTCTCCTCCACCAAC | 137886 |
rs550129772 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422386 | CAGGAGCCAAAGTCA[C/G]AAGAATCCGAGGAAA | 137886 |
rs550158587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426298 | TGTAAGCTCCGCCTG[C/T]TGGGTTCATGCCATT | 137886 |
rs550235243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421236 | AGAAAGTCCTACACA[C/T]GTTTTCTCATCCCCA | 137886 |
rs550259541 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449528 | GGACATAATTCCAAC[C/T]GTGCACTTGTGAACC | 137886 |
rs550305228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428053 | ATCAAATGTTTCAGA[A/G]AGTGTTTAATAACTG | 137886 |
rs550328561 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441182 | AGGTTTTGTAGAGAC[A/G]CGTGTCTTACTATGT | 137886 |
rs550380969 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449911 | TTGTGGGTCTTTTAC[A/G]TATGTCACAGGGATG | 137886 |
rs550421156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420400 | AGTGGGCAAAAAGGC[A/G]ATTAAGTGAATCTCT | 137886 |
rs550495048 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420961 | ATATGTAAAACTTGA[-/T]TTCCCCCAACAACAT | 137886 |
rs550533872 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426268 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 137886 |
rs550762108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422293 | AGTGAGAATGGCAGC[C/G]AAACTAACTCAGGGT | 137886 |
rs550770868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422847 | TCTTTATTTCTCAGT[C/T]TTTCAGCTTGTCTCA | 137886 |
rs550981203 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450372 | AAAAGTTCTGCTTTA[C/T]ACATAACGGCAGGAC | 137886 |
rs550983427 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450848 | ACACTGGGAGTGCTA[C/T]CAGAACTACCACAGG | 137886 |
rs551251181 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431540 | GCAATTGGGTACAGG[-/T]TTTTTTTACTCACTT | 137886 |
rs551267182 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448755 | TTTCTGCTGAAGCCA[A/G]AAGCTTTTCCTTCTT | 137886 |
rs551350332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414955 | AAAGCAAAAAGTGTT[C/T]AACAAATATAACCCC | 137886 |
rs551430298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421525 | AACCTAGAAGTAGAC[A/G]AATACCATGTATTTG | 137886 |
rs551554324 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426718 | GCTCCGTGACAGACC[C/T]GTTCCTTGCTCAGGC | 137886 |
rs551571970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442404 | TTAGAAAGTAACTTT[C/T]TAAAATGGCTTGGTT | 137886 |
rs551610924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415963 | TGTTCTTCTTGGAGG[C/T]AGTTTTCATATCATT | 137886 |
rs551657684 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449735 | GCTCACTGCTGTTCT[C/T]TGGGCTTGTTGACTG | 137886 |
rs551833357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443293 | AGTTTGAAGAAGAGG[A/G]TGTTTCTCCTGTCTC | 137886 |
rs551885246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428472 | CTTTTTCTGATTCCT[C/G]TGGTCATTTTGATGT | 137886 |
rs551893370 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409718 | GCACGCGCCACCACG[C/T]CCAGCTAATTTTTGT | 137886 |
rs551894099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435361 | CATGAATTTTGAATT[C/T]AAATTATATACAGAT | 137886 |
rs551946312 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440976 | CGTCTCTCTTTACAC[A/G]TCAGGCTTCTCTTTC | 137886 |
rs552121388 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411665 | CAAGTGCCCAAGCCT[C/G]CAGCGCTGGTGCTTT | 137886 |
rs552174117 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411180 | AGCAACACAAAACTT[A/G]ACAGAGGTTTCCCTG | 137886 |
rs552236656 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431605 | TGCAATTGGTAGATC[A/G]TACATTAAGTGTATG | 137886 |
rs552289306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427621 | GGAAGACTTAAATGT[C/T]TTAAATTTGGGATAC | 137886 |
rs552334412 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428919 | TTTATGTAGAGAAAA[A/T]ATAGTTCTTGTCCTC | 137886 |
rs552498884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424793 | CTTCTTCAATCCTGC[A/G]CTGTAGTGTTTCAGT | 137886 |
rs552567170 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444509 | AAATGAAATAATGCA[G/T]GTGGCAGAGGTGGTA | 137886 |
rs552617289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445215 | GGGCTAAGACAGCAA[C/T]GCCAGGGTCACTAGT | 137886 |
rs552627552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436368 | GAGTTAGGTTTTAGG[A/G]TCAGACAGTATTATC | 137886 |
rs552658336 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410505 | GAGATCTGCTTTTTT[G/T]CTTTTTTGAGACGGA | 137886 |
rs552726598 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424011 | TCAATGCCAATGCAA[A/G]GGTAGACCAGTCAGC | 137886 |
rs552740850 | snp | A/G | 3.90351e-05 | 0.00441769 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430681 | TAAGGTCAGTGCTCA[A/G]TTTTAAACTAAATAC | 137886 |
rs552880903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436911 | ATTACCCAGCCTCAA[C/G]TATTCCTTTATAGCA | 137886 |
rs552887938 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426556 | CATTTCTTCTAACAA[A/G]AAGTGTGAAGTCTCC | 137886 |
rs553007923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421770 | CACCTTTTACCAAAC[A/G]CATGATAAGCCTTAG | 137886 |
rs553019573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415106 | AATCTAGTTGGGGAA[A/G]TAAAACAGCAAAAGT | 137886 |
rs553045930 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442636 | CATAATAGAAGAAAG[A/C]AAACCATAGATATAA | 137886 |
rs553058315 | in-del | -/AAAAAAC | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451198 | CTATAGATGCACATA[-/AAAAAAC]CAAAAACAACTGCCA | 137886 |
rs553144705 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426791 | GCTCGGGACCAGATG[C/G]GGGGCGGAGCCAGCC | 137886 |
rs553379373 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432554 | CACCCAGCTAATTTT[G/T]TGTATTTTTAGTAGA | 137886 |
rs553418281 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429806 | TTACCCTGGAAGTCT[C/T]CATGTTGATACTTCA | 137886 |
rs553421359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441848 | AGATTTTGATTATGG[A/G]AAACAGAATCTACTT | 137886 |
rs553477010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417659 | ATCCCTGGGGAAGAA[A/G]CGTCAGTTTTCCCAT | 137886 |
rs553503580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445548 | GATTCAAAATGATTG[A/G]TGTACTTACTCAACT | 137886 |
rs553546612 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410062 | CTCTTTTCCCTACTA[A/G]ACTGAGTTTCATAAT | 137886 |
rs553551256 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417337 | TCAAAACAACTTTCA[C/T]GTGCAAGTTTGTCAT | 137886 |
rs553609099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435508 | ATGGTTTAAGTCAAT[C/G]CTGTGGACTTGGAAA | 137886 |
rs553671990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428749 | CTGCTGCATGCAAAG[A/G]CTTATTGTAAAGCTG | 137886 |
rs553997814 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58416792 | ATACATAACTTCTAG[C/T]TGTATGGAAGAGGTT | 137886 |
rs554134382 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58411378 | CGGGCGCCGCTAGCC[A/G]GCGGAAGATGGCGGA | 137886 |
rs554209454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418698 | ACTCCATTGTAAGAT[A/G]CTGTGTGTCCTTTGT | 137886 |
rs554215323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430175 | ACTATCTTTTGACTG[C/T]TGACACTGCTTTTCC | 137886 |
rs554215545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425344 | TCTTGGAATACCATC[A/C]GCCAAAAGTCGTTCA | 137886 |
rs554310766 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451862 | TCAGTTATCTCTGCT[C/T]ACTGAGATAAAGGCC | 137886 |
rs554349318 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423421 | AAGAACAGTTGGGGG[G/T]GGGTTTTTTTTTTGT | 137886 |
rs554366539 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438957 | TTGGTGCCATCCCCA[A/T]GGTAATGAGTTCTCA | 137886 |
rs554432474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446674 | ATTCCTATGATAGCA[C/T]ATTTCATAGTTTTAG | 137886 |
rs554436931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443911 | TCTGTGTGGTTCTGA[A/G]CATGTCTTTTAGTCT | 137886 |
rs554474768 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411674 | AAGCCTCCAGCGCTG[G/T]TGCTTTGTCTCCCTT | 137886 |
rs554545732 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414493 | GAAAGATTATCAATA[C/T]TTTACTTACATACTT | 137886 |
rs554556631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417246 | AATACTATTTTTCTT[A/G]GGCACAATGGTTCTT | 137886 |
rs554676645 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418535 | AGATCACTGTTTCCT[C/T]ATGATTAGATTTTTA | 137886 |
rs554699499 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423697 | GCCTCGGCCTCCCAA[A/C]GTGCTGGGATTACAG | 137886 |
rs554723428 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436193 | GTCAGCTTAATTACT[A/T]CAAGTAGCATTGCAT | 137886 |
rs554829437 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58415291 | TGAGAATAGGAATAT[C/T]ATAAAAGTAATTCAT | 137886 |
rs554874426 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410037 | AGCTGCATCTTACCC[A/G]TTTACATGTCTCTTT | 137886 |
rs554961330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429435 | CCATAGGCTCCTGCT[C/G]TAGATAAATTTGGGC | 137886 |
rs555144713 | in-del | -/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411235 | AGGAGAAACCAAAAA[-/G]GTGGGCCAGCACCGG | 137886 |
rs555156705 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411334 | TGCCAGGCAACCGGC[C/T]CCGGAAGTTGCGGCA | 137886 |
rs555222683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431088 | CTGAAACTCTCCTTC[A/G]TAGCCTACCATTTGC | 137886 |
rs555282405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425500 | TCACCATCGTGTAGG[A/G]CAACCCTGGTATGAT | 137886 |
rs555283794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424838 | CCATATAGATAAATC[A/G]GTACTGTGTTTCTGT | 137886 |
rs555299476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446595 | ATTGAAGTAAGACCC[C/T]AATAGATATATTTAT | 137886 |
rs555359057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438169 | AGCCTTGGTGGCTTT[C/T]GCATGGTGTTAAGCC | 137886 |
rs555381984 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448095 | TATTACTAGTATCAG[A/T]AACTACAGTTTTGCC | 137886 |
rs555416430 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58444154 | GATTACAAAAATAAT[A/G]GGGAGGCAACTTGGT | 137886 |
rs555497846 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449147 | TAAATGAGGCCCACC[A/G]GATATCCAATCTAGG | 137886 |
rs555663951 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425155 | ATATTCCCTTGCCCA[A/G]CCTTTGAAAGTTTAA | 137886 |
rs555807430 | snp | A/G | 0.0134861 | 0.0810011 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410750 | TATGTGTATATATAT[A/G]TGTGTGTGTATATAT | 137886 |
rs555814904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420007 | TTATGTAGCCAGTTG[C/T]GGATACAGCCTTGAA | 137886 |
rs555868801 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411265 | GAAGCGGGGGCGCGG[A/G]TTCGGGTAGCGGGGA | 137886 |
rs555882026 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439655 | CCCCTGGAGCTTCAG[C/T]GCCTTGTTCATGGTG | 137886 |
rs555882755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439997 | CTTAGATTGCAGTTA[A/C]CATGTTTGTGGCCCT | 137886 |
rs555945709 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58415840 | AATGTTACTGAATGT[A/G]GGAGGGTAGGGGTAA | 137886 |
rs555946010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432469 | CTGACTGCAAGCTCC[A/G]CCTCCCGGGTTCACA | 137886 |
rs555962733 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431042 | CATTTCTCTCTGTCT[A/G]TGTCCTTTTATCACA | 137886 |
rs556036492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437464 | TCCCAAGTAGGTGGA[A/G]TTACAGGTGCTCACC | 137886 |
rs556108881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424967 | TATCAATCACAACGT[A/G]TGTCCCTGTCCGGCC | 137886 |
rs556159202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445645 | TAACTCAGAGTTGCT[C/T]GTATTTCTAAATAAA | 137886 |
rs556514639 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448281 | CAGGTTCAAAAGATT[C/G]TCCTGCCTTAGCCTC | 137886 |
rs556605720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411800 | CTTACTCCAGAAGAA[A/G]GGTTACTGTGGCCGC | 137886 |
rs556640968 | in-del | -/AG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443739 | TTGAACTCAGGAGGC[-/AG]AGAGGTTGCAGTGAG | 137886 |
rs556662628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419422 | CAAGACAGTTTCATT[A/G]TCTGAAACTCTGGAC | 137886 |
rs556704202 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423928 | AACTGTAATTGGTCA[C/T]CGGCTGGAAAAAAAA | 137886 |
rs556743870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414271 | CTACCCCAGAGTGTG[A/G]TTCATTGGTTCTAGA | 137886 |
rs556755665 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448557 | TCCTCCCAGAGCTTG[C/T]GTTGATCACATTCAT | 137886 |
rs556940594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426451 | CTGACTTTGTGATCC[A/G]CCCTCCTCAGCCTCC | 137886 |
rs556957405 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432414 | TTGAGACAGGGTCTC[C/G]CTCTGTTGCCCAGGC | 137886 |
rs557007164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415015 | TCTGATTCATTTTCT[A/G]TTATGTTCTTTATAT | 137886 |
rs557018975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421587 | CCATTACTGACTGGG[C/T]TCTCTCATTACTGGC | 137886 |
rs557089155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427336 | AGCGTGGTGGTGCAC[A/G]CCTGTAGTCCCAACT | 137886 |
rs557152518 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427729 | AGAACTATCTAGCAG[G/T]TGCTTTTAAATTCAA | 137886 |
rs557203040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420773 | GTTCAATAGTTTTTG[A/C]CTTGTGTGAACTGCC | 137886 |
rs557228197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433834 | TTATTATTATAAATG[A/G]TATATTTTCATAATC | 137886 |
rs557263604 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437241 | AAAGGACTTGTCTGC[A/G]TTGTGTCCATACCCT | 137886 |
rs557293114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440911 | CTGTTTTTCTTAGGA[C/G]ACAAACTCTTTAATT | 137886 |
rs557371707 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426759 | TCGGTCACGTTGGGC[A/T]GGCCCGAGGGAGGCC | 137886 |
rs557532521 | in-del | -/CTTC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429323 | CCCTAAAATAATCTG[-/CTTC]TAACACTAAGGCTTG | 137886 |
rs557551873 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422516 | ATAAGGCGAAGAGGG[A/T]TGTCTTTGGAAAAGG | 137886 |
rs557673441 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420130 | TAAAAGCTTTGACTC[A/G]AGATGGATACATCTC | 137886 |
rs557704504 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448465 | AGGCATGAGCCACCA[C/G]GCCCAGCCTAAAGGT | 137886 |
rs557736624 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438846 | TGGTTTGGATGTTTT[C/G]TCCCCTCCAAATCTC | 137886 |
rs557744066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432197 | ATTTTCTCCTTTGTT[A/G]TCTGGAAAAATGTTA | 137886 |
rs557755334 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449273 | ATTAACATTTTACAT[A/G]GAACATTATTCTTGC | 137886 |
rs557805702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426398 | ATTTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 137886 |
rs557861492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414143 | TGTCTGATAGCTGTT[C/G]TGATAACTGTGTTGC | 137886 |
rs557993714 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448319 | GCTGGGATTACAGGC[A/G]TGCGCCACCATGCCT | 137886 |
rs558007932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425920 | ACTGGTGCGCACAGA[A/G]AGAACAAAATCTCCA | 137886 |
rs558017633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440732 | GCCCCCTTCAGTTGC[C/T]TCGTGTACACTGGTT | 137886 |
rs558081533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433504 | TTGCAGCCAGGCGTG[A/G]TGACATGCATCTGGA | 137886 |
rs558282352 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432907 | TTTAAAAAAGCCTCT[A/G]TGATAATTTTGACAT | 137886 |
rs558288258 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58430049 | ATCTCTGAAAGATAA[A/C]TCCTCTCTAGATAAC | 137886 |
rs558345962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426852 | GGATCCTGGAGACTG[C/T]GCAGCCGCCCCCTAG | 137886 |
rs558347343 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427322 | CAAAAAAATAGCCAA[A/G]CGTGGTGGTGCACGC | 137886 |
rs558430680 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450523 | ATCGAGGTATTCTCT[A/G]TTATGCTCCTTTCTT | 137886 |
rs558496373 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426697 | TCATGTTCCTCCCAC[A/G]TTCCGGCTCCGTGAC | 137886 |
rs558591268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415403 | AACTTTAGACCCTAG[C/T]CATCAGACTGTGTAT | 137886 |
rs558674707 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443800 | GCAACAGAGCAACAC[C/T]GCATCCCAGAAAAAT | 137886 |
rs558726109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422443 | AGCATTTTATTACCA[C/T]CACAAAAGTCAATTA | 137886 |
rs558743106 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451088 | TTGAACATTGTAAAT[C/T]AAAGGGCATTGTCCT | 137886 |
rs558923134 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426347 | GAGTAGCTGGGACTA[C/G]AGGTGCCTGCCACCA | 137886 |
rs558971666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423856 | GAAGACAGTTACTCA[A/G]ATGCAAAGAAAATAT | 137886 |
rs559089483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413761 | ACAAACTGCAGACTC[A/G]GAAATGTTTTTTTGC | 137886 |
rs559093370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBXN2B | GRCh38.p7 | 8:58435086 | TGATAATAAAAGCTT[G/T]TCTGTGTTATGATTA | 137886 |
rs559158264 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413767 | GCAGACTCGGAAATG[-/T]TTTTTTTGCATATCA | 137886 |
rs559242127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424551 | GGAGAGAGTGAAGTC[C/T]ACATCTATTTTTGTG | 137886 |
rs559334595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422118 | GCTTCTTGCTGCAAA[C/T]ACTGAACTGGAATCT | 137886 |
rs559375334 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420266 | CTAGCAAAGCAGTTG[C/T]GCTAACACCCATAAA | 137886 |
rs559412135 | in-del | -/TAT | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441316 | TCTCAAATTGTATAA[-/TAT]TATGTTTTTACTCCT | 137886 |
rs559436701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413053 | TAATGACCACCTGAT[C/T]CTTGGCAAATTGTTT | 137886 |
rs559463383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440392 | CCAAACCCTTTTTTC[A/C]AGTCATGGAAGTGCA | 137886 |
rs559470998 | snp | C/T | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426502 | TGTGAACCACCGTGA[C/T]CGGCCCAGTGTTCTG | 137886 |
rs559529959 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420911 | ATACAGATCCTGACA[A/G]AGGCATCCTGACATC | 137886 |
rs559562234 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449419 | TCAACTCTAAATCCA[A/C]AATCTTATCTGAGTC | 137886 |
rs559568691 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450243 | TTATATTTAACAGGT[C/G]TTCCCTCAATCTACC | 137886 |
rs559600502 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422710 | AGTGGGGTGGTGCTG[A/C]TTTCAAAAGCCCTGA | 137886 |
rs559680127 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432679 | GAGCCACCTCTATAC[A/G]GCTTTTATAATTGTT | 137886 |
rs559696704 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448700 | TGTAAATTCTGTCAG[A/G]CGGACTAGATCTAAA | 137886 |
rs559743690 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444065 | CATTTTCTTACCTAG[C/G]TTCCCCATCCTCCAT | 137886 |
rs559827028 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450640 | ATTCTTCCAGCCTCC[A/C]CCTACTGCCCAATTC | 137886 |
rs559898255 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416568 | TAAATTTGAAAATGG[A/T]TTGTTACCTAAAACA | 137886 |
rs559987235 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425767 | TGTTTCCATCATAGG[A/C]TTCTTCTTGTAATGT | 137886 |
rs560048586 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427261 | GATCGCTTGAGCTCA[C/T]GAGTTCAAGACCAGC | 137886 |
rs560177681 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428374 | TGAGATTAGAAAAAC[A/G]AAAGTATACAAATTG | 137886 |
rs560234443 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412921 | AGAAAGATGCTATAA[C/T]TTTCCCTGGCTAGTC | 137886 |
rs560244425 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428965 | ATAAACGTCAGTTCC[A/G]TATGGGTTGTGGATC | 137886 |
rs560334587 | in-del | -/TTG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413200 | TCATCTCCTGTCTAC[-/TTG]TTGTAGGTTAGGGCA | 137886 |
rs560424104 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410344 | CTTGAACCCGGGAGG[G/T]GGAGGCTGCAGTGAG | 137886 |
rs560454647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436811 | TTGTAAGTTCCCTGC[A/G]GCTTCACCAGAAGGA | 137886 |
rs560535415 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428268 | AAAAAGATTGAAACC[A/G/T]CTCAACTCTTCTGAA | 137886 |
rs560545823 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424694 | GTACAAGGCGGGGGG[C/G]GGGGCTCTGATCTCC | 137886 |
rs560548049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417546 | AAAACAACCAACTGT[A/G]AAGACTTAAGAGATG | 137886 |
rs560631761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445790 | CTTTAATATAATGAA[A/G]GAGGTTGAAAGAAGT | 137886 |
rs560753438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442111 | AGCTACAGAGTTTCC[A/G]CTTTGCAGTGCTTAC | 137886 |
rs560763219 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437755 | AGAGAAGCAGAGCCC[A/G]TTGAAGTTTGGAAAA | 137886 |
rs560780338 | snp | A/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444975 | ACTTTTATACTAGTA[A/G]TATGTAGATACATGC | 137886 |
rs560970040 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409856 | TCAGCCACGACGCCC[A/G]GCCTCAAATGCCTTT | 137886 |
rs561024712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415644 | TTATTTAATCCTTCA[A/G]ATGACTACGGTGATT | 137886 |
rs561045952 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449564 | AACAAGTTATCTGTT[C/G]CCAAGTATGATGGCA | 137886 |
rs561082652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428221 | AGTCGCAGATAATAT[A/G]TTTAAGGTTTGGGTA | 137886 |
rs561158906 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434381 | TATATTTTTTTTTTT[C/T]CTATACCCAAAAGGT | 137886 |
rs561231716 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410287 | GCATGGCGGCACGCA[C/G]CTGTAGTCCAAGCTA | 137886 |
rs561294709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423879 | GAAAATATGGCAAAC[A/G]TTTTCCCACCACAAC | 137886 |
rs561299371 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429880 | AGATAAAAGTAGGTT[A/T]TTAATCTTACGTAAA | 137886 |
rs561351813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436124 | CTGTGCAGTCTAGCA[C/T]TTCCTATGTAAATGT | 137886 |
rs561356818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417432 | TCCATTTAAGAATCT[A/G]TGATTTTTGAAGTCT | 137886 |
rs561362788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428874 | AGTGAGGGGCAGAAT[C/T]TCATTAGGTGGTACT | 137886 |
rs561363531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424713 | GCTCTGATCTCCACT[C/T]GTCTGGTCCGCTAGA | 137886 |
rs561541937 | snp | A/G/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449241 | CTAAGGTTACATACA[A/G/T]GTTTGGAGATTAGGA | 137886 |
rs561560659 | in-del | -/TAT | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439959 | TAATATTAATTGTGA[-/TAT]TAATAATACTGTAAT | 137886 |
rs561736175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419446 | TCTGGACATAAGATG[A/G]TCTGTGTTTTTAATT | 137886 |
rs561775907 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447698 | TCTGTCTTCCAATCT[G/T]AATATAGACAAATTT | 137886 |
rs561782033 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445551 | TCAAAATGATTGATG[C/T]ACTTACTCAACTTTA | 137886 |
rs561814542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436806 | CATGATTGTAAGTTC[C/T]CTGCGGCTTCACCAG | 137886 |
rs561855013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437390 | TGGAGTGCAGTGGCG[C/T]GATCTAGGCTCACTG | 137886 |
rs561921305 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58411436 | GGAGAGGAGGTCTTC[C/G]GGGCCGCGGCCTCCG | 137886 |
rs562054632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418992 | CAAATATAATCATTA[A/G]GATATTTCAGTGAAG | 137886 |
rs562097750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431852 | GCTAGTGATGAACAT[C/T]GTTTCATGTGCTTCC | 137886 |
rs562114776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58435941 | CTCAAAGAAGAACTC[A/G]TAGATAATATAATCT | 137886 |
rs562236492 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439102 | TGTAAGTTTCCCGAG[G/T]TCTCACCAGAAGCAG | 137886 |
rs562251427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444168 | TAGGGAGGCAACTTG[G/T]TGTGTAGAAAGAGCC | 137886 |
rs562359185 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411748 | CATTTTGCGGGGTCA[G/T]TTGGTCGGTTCACGG | 137886 |
rs562377174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429042 | TTATGACCTTAGAGT[A/G]GGCAAAGATTTCAAA | 137886 |
rs562537367 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437047 | TGGAAGACTTTGGAC[A/G]TCCTTGAAGAAGATA | 137886 |
rs562593811 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434055 | AATGAAGGAAGTGGG[A/T]ATCATGGAGTACAGC | 137886 |
rs562597095 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445035 | TAGGAAACCATCTAA[A/G]TCTCAGAGTTCAAGA | 137886 |
rs562665468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424697 | CAAGGCGGGGGGGGG[G/T]GCTCTGATCTCCACT | 137886 |
rs562691712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418172 | CCTGATCTTGGGAGG[C/T]AGAAGTTGCAGAGAG | 137886 |
rs562797692 | in-del | -/ATG | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425440 | GTTTCAAATTTGGGC[-/ATG]ATGATATTTGCATTG | 137886 |
rs562946494 | snp | A/G | 6.68963e-05 | 0.00578305 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58446038 | TAGCAGATGGGAGTC[A/G]TTTGATACAAAGATT | 137886 |
rs562953290 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411100 | TTTCATTGTTGAGCT[A/T]AATGAATCTGCAAGT | 137886 |
rs562953392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418821 | GCTTCTTTAATTTGT[A/G]TATTCTCCCAAGTCT | 137886 |
rs563014303 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58411403 | GGCGGAGGGCGGAGG[C/T]CCTGAGCCCGGCGAG | 137886 |
rs563048811 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446955 | ACAGCCACCACCATG[C/T]CCAGCTAATTTTTTC | 137886 |
rs563094418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425998 | TTCAGTTAATAATTT[A/C]TCTGCTTCTTTCCCA | 137886 |
rs563107086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431163 | AATACCAGTCGGGTT[A/T]TCATCTCTATAATTT | 137886 |
rs563161873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420221 | TACAGTTTACAAATA[C/G]ACTTTTACTCTGATA | 137886 |
rs563192890 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58435777 | AATTTGAGCCACACC[A/G]TATCTGCAATAATGT | 137886 |
rs563258154 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419583 | TATGTCCTCCACAAG[C/T]CATTGTATAGTAGTA | 137886 |
rs563312122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439269 | CCATATCAATTTTCA[A/G]AACTTTCTCCGAGGA | 137886 |
rs563313647 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432599 | ATGTTAGCCAGGGTG[G/T]TCTCGATCTCCTGAC | 137886 |
rs563317939 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419963 | TGAACAAGGGGACTC[A/G]ATTTTCACTTTGCAC | 137886 |
rs563374907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426621 | CTGTCAGCTCCTCTT[A/G]TCAACAGTGGGTTTT | 137886 |
rs563379235 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448587 | TTTATTCATTCAACA[C/T]ATTTTTCTAGGAAAC | 137886 |
rs563392154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425593 | CGGCCGTAGAGAAGT[A/G]TGCACTCCTGTTGTT | 137886 |
rs563636350 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426862 | GACTGTGCAGCCGCC[C/T]CCTAGGCTGGCTTGC | 137886 |
rs563688387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422006 | AAACTCTTGTGTGCT[A/G]GTGAAAGACTTTACC | 137886 |
rs563690724 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424828 | TGCTGGACCGCCATA[C/T]AGATAAATCGGTACT | 137886 |
rs563753367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414762 | TAAGTTTTTAATGAT[G/T]TACCGTTAATAACTA | 137886 |
rs563754781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419083 | GTTTGTAAGGATTTT[A/G]TGCCTCACATTTGAT | 137886 |
rs563944810 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412889 | CTGGGCAAATATTTG[A/T]TTCCTTTTTCCTCAG | 137886 |
rs563987986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447126 | TTAAAATAACAACAT[G/T]AGTACACTTACTTTA | 137886 |
rs564176156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440294 | TCACAACTTAAGCAT[A/G]CATGTCTGCCATCAG | 137886 |
rs564197258 | snp | A/G | 1.69269e-05 | 0.00290915 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430632 | GGGCTGTCCCTCTGA[A/G]TGAAGCCACAAGAGC | 137886 |
rs564258336 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421636 | CTCAGCAACCACCTC[C/T]TTGGAACTTTAATTT | 137886 |
rs564335399 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418220 | CACTCCAGCCTGAAT[C/G]ATGGAGAAGGACTCT | 137886 |
rs564446482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411976 | ATGCACTCTATGCCC[A/G]TACAGCCTAGTTGTC | 137886 |
rs564539846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431888 | ATTATCTGTATTATT[A/C]TTTTCAAGGAAATAT | 137886 |
rs564623108 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432573 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 137886 |
rs564768333 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449498 | GTTTGGGAGAGGATC[G/T]GTGTGTGATTTCTGG | 137886 |
rs564771319 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449464 | GTCTCAAATCTCACA[C/T]TGAAGCCATCTAAAT | 137886 |
rs564799963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426292 | GCTCACTGTAAGCTC[C/T]GCCTGCTGGGTTCAT | 137886 |
rs564881990 | in-del | -/G | 0.398483 | 0.201129 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424689 | TTGGAGTACAAGGCG[-/G]GGGGGGGGGCTCTGA | 137886 |
rs565046060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441992 | CCAGAGAAAACAACT[A/G]TGTCCCCTAGTCAGG | 137886 |
rs565094078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422831 | CTTCTTGAAGACCCT[C/G]TCTTTATTTCTCAGT | 137886 |
rs565111129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434307 | ATATCACATTTGGAA[C/G]TTAAAATTATTTGGG | 137886 |
rs565187779 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450034 | ATTCACACCCTTAAT[A/G]TCTTCAAAGAGTCTT | 137886 |
rs565221606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416680 | TTGGTTAGTTCTATA[C/T]AATGAGATGCAGTAA | 137886 |
rs565234771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427380 | AAGTGGCAGGATAGC[C/T]TGAGTCCAAGAGGTG | 137886 |
rs565316604 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450775 | AGATTTGGAATTCAC[C/G]TTTCTCCAGGGTCAC | 137886 |
rs565343625 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432458 | CACCATCTGGGCTGA[C/T]TGCAAGCTCCGCCTC | 137886 |
rs565470612 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58430274 | TCAGCAAGCAAGCCA[C/G]TTGCCGTGCTGGAGG | 137886 |
rs565514957 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451398 | AAAAAAGATGTCACA[A/G]TGAACAGACAACCAT | 137886 |
rs565566099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426361 | ACAGGTGCCTGCCAC[C/G]ATGCCCGGCTAATTT | 137886 |
rs565615644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412404 | CTACCTTTTGGAAGC[C/G]TACAGATTTCTTCGG | 137886 |
rs565650071 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450554 | CAAGGCCGCCCTAGC[A/G]TTAACATTCCATATT | 137886 |
rs565655095 | snp | C/G/T | 3.31533e-05 | 0.00407134 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447436 | CTCGTCCTGAATTTG[C/G/T]GGCTCTTGACTTTAT | 137886 |
rs565692706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421394 | TTGTCTTTTTTAAAA[A/G]AACCCAATACCATGT | 137886 |
rs565702613 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431991 | TTAATAGGTATGGGT[A/C]CTTTGTCAGATACAT | 137886 |
rs565754713 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421980 | AATACCGGAGATATA[C/T]TTGTACAATCAAACT | 137886 |
rs565827762 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420517 | TTAAAAGATTTATCA[A/G]TAAAATATTAAATAT | 137886 |
rs565892271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432625 | CTGACCTCGTGATCC[A/G]CCTGCCTCGGCCTCC | 137886 |
rs565979519 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417570 | AGAGATGAGAACCAG[G/T]TGTCTTTTATTGCTG | 137886 |
rs566016760 | snp | A/T | 0.000133085 | 0.00815627 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58445959 | GAAGAGGAGGATAAA[A/T]CAATACTTAATGCAG | 137886 |
rs566045515 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449258 | TTTGGAGATTAGGAC[A/T]TTAACATTTTACATG | 137886 |
rs566192367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441198 | CGTGTCTTACTATGT[C/T]GCCCAGGCTGGTCTT | 137886 |
rs566311871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423584 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCTGC | 137886 |
rs566344667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414852 | TGTATGTTCCACATT[C/G]CATGGGGCTAGTGGC | 137886 |
rs566404432 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428541 | CCTTGTCCTCTGTGC[C/T]TATCTAAGTCCTAAT | 137886 |
rs566456059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433455 | ATATGGAACTATTTG[C/T]TGAAAGAATGTGTGA | 137886 |
rs566500723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416093 | ACCGGAGATTATGGT[C/G]ATGCCAATTATAATT | 137886 |
rs566621644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423656 | TAACCAGGATGGTCT[C/T]GATCTCCTGACCTCA | 137886 |
rs566688884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417012 | TTCTAAAAATTTACT[A/G]ACTTCAAATTATTTT | 137886 |
rs566758324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424473 | AGTCAACCACAATGC[A/C]AGCCTTCCAAATCCA | 137886 |
rs566762814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423023 | AAAATCTGGTCTGGG[C/T]ATGTGACTTGTTTAG | 137886 |
rs566798564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432584 | AGACGGGGTTTCACC[A/C]TGTTAGCCAGGGTGG | 137886 |
rs566919782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444414 | TGCCTGGTGTTACAG[A/C]ATAAGTGCAGAGTTG | 137886 |
rs566935235 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409894 | AAAACGATCAGTATG[C/T]CAAAGCTCGGGCGGC | 137886 |
rs566946408 | in-del | -/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413176 | AAGTTATGATGGGGA[-/T]TTTTTTTTTCATCTC | 137886 |
rs566963346 | snp | A/G | | | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435232 | GAGTTATATATACAG[A/G]GTTATACTCCATAAA | 137886 |
rs566984985 | in-del | -/TAA | 0.00201491 | 0.0316764 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430002 | AACAAACGCAGGGGC[-/TAA]TTTTAAGGGAGTAGG | 137886 |
rs567027429 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429286 | GGAAGTGTTGCTTTG[C/G]TTTTCTGTGTTTGTC | 137886 |
rs567098504 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449417 | CATCAACTCTAAATC[C/T]AAAATCTTATCTGAG | 137886 |
rs567187638 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423930 | CTGTAATTGGTCATC[A/G]GCTGGAAAAAAAAAA | 137886 |
rs567201963 | in-del | -/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448993 | CCTTGTCATTCCACC[-/T]TCTACAGGACATCCT | 137886 |
rs567254319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440612 | GTTACCCTCTACTCG[A/T]CCACATATTGTTGCA | 137886 |
rs567300648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433377 | GTTAAAAGGACCAAT[A/G]ATGTGTGAGTTTTCA | 137886 |
rs567364112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415028 | CTATTATGTTCTTTA[A/T]ATAATTCAACGTCAA | 137886 |
rs567558072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427102 | AATTAATGAGGATGG[A/G]GAGAACAGGATAAAG | 137886 |
rs567621338 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434677 | AGGATATACTGCTAT[A/C]TGTATGTAAGTCACT | 137886 |
rs567649776 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450407 | CTCAGCTTAGCTTTT[C/T]GCCACTATGTAACAA | 137886 |
rs567674320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424341 | CTATAAAATATAATG[C/T]CTACATAGTAGAGAT | 137886 |
rs567728032 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432320 | GTTGCTCCAGCATCA[C/G]TTCTTGAAAGGCACT | 137886 |
rs567809321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429121 | CCGATTTTTGCGGTA[A/G]GGTCTTTCTCACTAA | 137886 |
rs568037458 | snp | A/G | 0.00478085 | 0.0486577 | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451958 | CCTACCTGTGCCCTG[A/G]AAGTCCTCTCCCACA | 137886 |
rs568061725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417633 | AACATCTTTTTAGTA[C/T]TGTAAATACCATCCC | 137886 |
rs568327897 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437956 | TTTAAGGCAGCCCCC[A/C]CCCCAACCCCCATCA | 137886 |
rs568463650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446177 | ATGATATTCTTTAGG[A/T]TTACTTTTGAAGTAA | 137886 |
rs568493179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430951 | GTACCTTTCACTTCA[A/G]TGGTTTCCCCCAATG | 137886 |
rs568729699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423279 | ACTACACGAAGAAGG[A/T]GAGACTCAGGACTGC | 137886 |
rs568758403 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425253 | TTTTAGAGCATACTC[A/G]TCAGGCCAGTATTTG | 137886 |
rs568805802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428589 | GGCCCAGCTGAGTAC[A/T]AATTCTGTACTACAG | 137886 |
rs568865779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427631 | AATGTTTTAAATTTG[C/G]GATACAGGAAAAAGT | 137886 |
rs568940687 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451139 | GAAAAATAACCAATC[A/C]TTGTAAAATTATTTG | 137886 |
rs568941432 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438565 | TCTGTGGGGCCTGTT[C/G]CCTCTTTCTTTTGGC | 137886 |
rs569025588 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431648 | AACAGCCAAACTATT[C/T]TCCAGAGTGGTTGTG | 137886 |
rs569034804 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409972 | CGGAGTATTTCCCCT[C/T]ACATGGCTCACATTT | 137886 |
rs569140394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445280 | TTCATTATGAATTTA[C/T]TGTCATGTAATAACA | 137886 |
rs569175933 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58435778 | ATTTGAGCCACACCA[C/T]ATCTGCAATAATGTA | 137886 |
rs569209810 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417482 | GATGATTCCTCTAAT[A/G]TGTGACCTCCTAAAT | 137886 |
rs569224289 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414354 | ATCATTTATTACAGC[A/G]TCTAGAATTGGTTAC | 137886 |
rs569272163 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411573 | CTCGGCGGAGCCTTT[C/T]CCCGACCCCGTCTGG | 137886 |
rs569353114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444539 | AATGGTGGTAGTGAC[C/G]ATGATAATGTGTATA | 137886 |
rs569404089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424816 | GTTTCAGTATAATGC[C/T]GGACCGCCATATAGA | 137886 |
rs569409387 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411268 | GCGGGGGCGCGGGTT[A/C]GGGTAGCGGGGACGC | 137886 |
rs569469677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418594 | AGTGATATTGTCTGC[C/T]ATTTATTACATGACA | 137886 |
rs569480935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438660 | AATAGTTAATTTTTT[A/G]TCTTACAGGATTATA | 137886 |
rs569606621 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429141 | TTTCTCACTAAGACT[A/G]AGATAAAAAGGAATG | 137886 |
rs569621197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438158 | CCACTACTGTAAGCC[C/T]TGGTGGCTTTCGCAT | 137886 |
rs569638002 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431863 | ACATCGTTTCATGTG[C/T]TTCCTTGCCATTATC | 137886 |
rs569650757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419176 | AACTGTGTTTAATCT[A/G]TTTATAATACAATGT | 137886 |
rs569731376 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447651 | AAATTATTTTTATTA[C/T]TTTTACAGATAAATT | 137886 |
rs569857827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447285 | AAGTTACAACACCTT[C/T]ATATAAAGATTAAAA | 137886 |
rs569984409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420467 | ACATTTACATGATTC[A/G]CATCAAAATGATGAC | 137886 |
rs570113052 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58447140 | TTAGTACACTTACTT[C/T]ATTCATAACTTACCT | 137886 |
rs570199850 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449034 | CTTGTGACCTCCTTC[G/T]TCCATCTTAAAAACC | 137886 |
rs570223190 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413983 | TTGTATACTCTGTCC[C/G]AGTTTTCCTCCACAT | 137886 |
rs570297109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446224 | ACATTTTTAAAAGGA[A/C]AATAGCTGTGTTTAA | 137886 |
rs570318371 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412188 | ATTTGACAAGTAAAT[A/G]TCAGTAAGGAGATAC | 137886 |
rs570362186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413240 | GATAACTGATTTCTT[G/T]ATGAATGTGATTTGG | 137886 |
rs570429787 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441423 | GTATGTATGTTCTTA[A/G]TTTTGTATCACTTCC | 137886 |
rs570448178 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411246 | AAAAGGTGGGCCAGC[A/T]CCGGAAGCGGGGGCG | 137886 |
rs570596170 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427972 | ACAAACAATTTTGGT[A/G]TGAAAGTCCAGGAGA | 137886 |
rs570621620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438600 | CTCTCTTTTGGAATG[A/G]GAATGTTTACCCAAT | 137886 |
rs571016315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420364 | TTTTAAAAAACAGTT[G/T]CAAATAGACTACATA | 137886 |
rs571067035 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446364 | AAAACTATATGAAGT[C/T]GAATCAGATTTAATT | 137886 |
rs571071442 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442872 | CCTGTTTGTCCTACT[A/G]TTCTCTTCAAAAGAT | 137886 |
rs571201270 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448861 | GCTTAAAATAGCACA[A/G]ATTTATTATCTTCAC | 137886 |
rs571260818 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441140 | ACTATAGGCACTGCC[A/G]AGCGCAGCTCATTTT | 137886 |
rs571309771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440529 | CACATGGCAGAATGT[A/G]TGAGTGGTTTCCTTT | 137886 |
rs571402181 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414152 | GCTGTTCTGATAACT[G/T]TGTTGCCACAAGTAC | 137886 |
rs571455793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427061 | TACTATTCATTTAGG[A/C]AAATAGGACTGGCAA | 137886 |
rs571484616 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450817 | AAGAGGTGAATTTAC[C/T]TGTGCTAGGGTTTTC | 137886 |
rs571595066 | in-del | -/ATA | 0.0568618 | 0.158738 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434367 | TATATATATATATAT[-/ATA]TTTTTTTTTTTTCTA | 137886 |
rs571692173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430421 | AATAATGCCTCTTTT[C/T]AAATAAAATACTTTT | 137886 |
rs571875295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419476 | TTACAAGAGGAGTTA[C/T]GTAATCTACAGAAAG | 137886 |
rs571923725 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438244 | CACCTAGATTTTAGA[A/G]GGCCACGCCAAAGGG | 137886 |
rs572010954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425526 | ATGATCAAAGGGCAG[G/T]TTATTTTTATATCTA | 137886 |
rs572106367 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447710 | TCTGAATATAGACAA[A/G]TTTGGATTAGGAATA | 137886 |
rs572115090 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418111 | CTGGGCATGGTGGCA[C/T]GAGCCTATAATTCCA | 137886 |
rs572183876 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419435 | TTATCTGAAACTCTG[A/G]ACATAAGATGGTCTG | 137886 |
rs572184054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446596 | TTGAAGTAAGACCCT[A/G]ATAGATATATTTATG | 137886 |
rs572189749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422898 | CTTCCCAAGGTCACT[A/G]GCAACTTCTGCTTTT | 137886 |
rs572229774 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444376 | CTGCTGTTGGCTCTC[A/C]GGCACAATAAGGGTA | 137886 |
rs572308000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431553 | AGGTTTTTTTACTCA[C/T]TTATGGTTTTATTTC | 137886 |
rs572361683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413327 | TGTGAAGAACTTGCA[A/G]AGAAACTTGAAAACA | 137886 |
rs572365314 | snp | G/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448442 | GCCTCCCAAAGTGCT[G/T]GGATTACAGGCATGA | 137886 |
rs572385027 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429404 | ACCCTTGAGTGTAAG[C/T]TTGGGACAAGGGCTT | 137886 |
rs572389458 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439978 | AATAATACTGTAATT[A/G]ATACTTAGATTGCAG | 137886 |
rs572438538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412841 | TATAAAGGGCCTATG[A/C]AAAATTCCTACATTA | 137886 |
rs572503476 | in-del | -/C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434381 | ATATTTTTTTTTTTT[-/C/T]CTATACCCAAAAGGT | 137886 |
rs572532113 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432529 | CTGGGACTACAGGCA[C/G]CCGCCACCACACCCA | 137886 |
rs572648107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432887 | TATGCCTAGAAACGT[C/G]TCTTTTTAAAAAAGC | 137886 |
rs572746578 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424315 | CTGCTTCCTCAATTT[A/G]AAACAAAATTCTATA | 137886 |
rs572783815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414519 | TACTTTATCCTCTGC[A/G]TATTATTGAAACATT | 137886 |
rs572848473 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421799 | AGCAACCTAGGGACT[A/G]TGATAACTCTGGCCT | 137886 |
rs572986048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426816 | CCAGCCGACTGTGCA[C/T]AGACCCCCCTCCAGG | 137886 |
rs573003652 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451407 | GTCACAATGAACAGA[A/C]AACCATCTGTGAGGT | 137886 |
rs573065796 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449953 | ATAGGAGGCTCCTCA[C/T]GTATCTTTCCTGGAA | 137886 |
rs573070767 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416569 | AAATTTGAAAATGGT[G/T]TGTTACCTAAAACAG | 137886 |
rs573074742 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423734 | GCCACCGCGCCCAGC[C/T]GGGGATGGGTTTTTT | 137886 |
rs573083464 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415167 | TGAATGTCATTGGGG[G/T]TATTACGTGCTATGA | 137886 |
rs573176706 | snp | A/G | 0.00185908 | 0.0304316 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434920 | AAATCTTTTAATGTG[A/G]CATTACTGCTGGCAG | 137886 |
rs573238434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427909 | GAGGAGGAGGAAGAA[A/G]ACTCAGTAAAATAGA | 137886 |
rs573279953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434133 | ACTTCGAGGCCAGGG[A/T]CCACCTGCAGGACCT | 137886 |
rs573326720 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450477 | TTTTTTACCAACAGT[C/G]TATTCATGATGATTT | 137886 |
rs573334766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441911 | TGTAGTTTATAGAAT[A/T]TCTGGAAGAGGCAAG | 137886 |
rs573397311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442765 | ATAGGGAGGACTAGC[A/G]AGTAGGCATTCTTGG | 137886 |
rs573404605 | in-del | -/ATAG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446597 | TGAAGTAAGACCCTA[-/ATAG]ATATATTTATGATTT | 137886 |
rs573582109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420787 | GCCTTGTGTGAACTG[C/T]CTGTAGTGAAAAAAG | 137886 |
rs573648128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426496 | TACAGGTGTGAACCA[C/G]CGTGACCGGCCCAGT | 137886 |
rs573785851 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432422 | GGGTCTCGCTCTGTT[A/G]CCCAGGCTGGAGTGC | 137886 |
rs573842014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413695 | TACCACCAGAGAAAA[A/G]CTGCATAGTTGCTTC | 137886 |
rs573859153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427804 | TCTGTATAGGAAGAG[A/G]TTATCTTTGGCAGTG | 137886 |
rs574094276 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450571 | TAACATTCCATATTT[C/T]TACTAACAGTCTGTT | 137886 |
rs574182977 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58433358 | GTTACTTTTTAAAAC[A/G]TGGGTTAAAAGGACC | 137886 |
rs574191170 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429426 | CAAGGGCTTCCATAG[G/T]CTCCTGCTCTAGATA | 137886 |
rs574436701 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409690 | TCAGCCTCCCAAGTA[A/G]CTGGGACTACAGGCA | 137886 |
rs574454768 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412693 | TCCCACCAATTTTGG[C/T]TTGCCTCTTAGTCCT | 137886 |
rs574739758 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436200 | TAATTACTACAAGTA[A/G]CATTGCATTCAAGGA | 137886 |
rs574890376 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411335 | GCCAGGCAACCGGCC[C/T]CGGAAGTTGCGGCAG | 137886 |
rs574987277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429574 | GGATCTTTTCCTTCC[A/T]TTACTGCAAAGTGAG | 137886 |
rs574989308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423926 | CAAACTGTAATTGGT[C/T]ATCGGCTGGAAAAAA | 137886 |
rs575024743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418666 | GTTCATTTGGTTAAG[A/G]TGCTGACCACCACAG | 137886 |
rs575070405 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410865 | CGTCCGCCTCGGCCT[C/T]CCAAAGTGCTGGGAC | 137886 |
rs575285702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415562 | TGAAACACTGATACA[A/G]TCATTACTAAACATT | 137886 |
rs575306542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422487 | TGAAATATCCACACT[C/T]GATGATTCAACATAT | 137886 |
rs575348236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416364 | CAGAAACTCATTTTC[A/C]TAAACACGATGAAAT | 137886 |
rs575391317 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443857 | TAACTTTTTAGGCTG[G/T]TTTTTTAATACCACA | 137886 |
rs575468322 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410807 | TTTTTTTTTTAGTAG[A/T]GAAGGGGTTTCACCA | 137886 |
rs575553121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435169 | AGTTGAGCATAAACT[A/G]GGGAATTAAGTTGTA | 137886 |
rs575560786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428830 | GAACTCAAGAATCAT[A/G]GGCAACTTGATTTAT | 137886 |
rs575595300 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58444012 | CAGTTCTCAAATGTT[A/G]TTATTCCATATACAA | 137886 |
rs575611219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436720 | GATTGTTTAAAAGAG[C/G]CTGGAACCTCCCCTT | 137886 |
rs575623848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423860 | ACAGTTACTCAAATG[C/T]AAAGAAAATATGGCA | 137886 |
rs575672791 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437471 | TAGGTGGAATTACAG[A/G]TGCTCACCACCACGC | 137886 |
rs575721226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417779 | ATATTCACCAAGTTG[A/G]TACAATGTTACATTG | 137886 |
rs575813526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58435609 | ACATAACTGTAGAAA[C/T]TGATACTAATTTCAA | 137886 |
rs575927638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445646 | AACTCAGAGTTGCTC[A/G]TATTTCTAAATAAAA | 137886 |
rs576092479 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58415898 | TATTTGTGTATATTT[C/T]AAAAGTTGACTAATA | 137886 |
rs576146278 | snp | A/G | 0.000497944 | 0.015771 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439806 | AAAATACCTTTGTTG[A/G]ACATGAATTTTTCTT | 137886 |
rs576153626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424969 | TCAATCACAACGTAT[A/G]TCCCTGTCCGGCCAA | 137886 |
rs576187604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425492 | CGTTGGGATCACCAT[C/T]GTGTAGGACAACCCT | 137886 |
rs576205298 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443858 | AACTTTTTAGGCTGG[-/T]TTTTTAATACCACAC | 137886 |
rs576212729 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418923 | CATAAGTTGAATGAC[A/T]TAATATTTGAGTTCT | 137886 |
rs576425072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444144 | GAAAGCAGTAGATTA[C/T]AAAAATAATAGGGAG | 137886 |
rs576449651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419426 | ACAGTTTCATTATCT[A/G]AAACTCTGGACATAA | 137886 |
rs576458417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419419 | AGCCAAGACAGTTTC[A/G]TTATCTGAAACTCTG | 137886 |
rs576537326 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438969 | CCATGGTAATGAGTT[C/G]TCACCCCGGTAGTTC | 137886 |
rs576619004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439842 | ATAAGAAAAGCAAAA[C/T]GACCTATGAAGTAAA | 137886 |
rs576629217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446998 | AGACGGGGTTTTCAC[C/T]GTGTTAGCCAGGCTA | 137886 |
rs576685377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444774 | ATTTTAACCTTATGT[A/G]TATTTTTATGTATCC | 137886 |
rs576728728 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419811 | TAGTAGCAAATAAGG[A/T]TGGATAGATGGGGGT | 137886 |
rs576752054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431806 | TTTATTTGTCTAATA[A/G]CTAATGATGTTAATT | 137886 |
rs576831320 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58439214 | GGATATTTCCTTATA[A/G]CAATGCAAATGGACT | 137886 |
rs576868443 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410140 | GCCTAGGAGGCCAGG[C/T]GCAGTGGCTCACGCC | 137886 |
rs577070503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415733 | AAGATCACACAGGAA[A/G]TGCCTAAGTTACGAT | 137886 |
rs577119854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427508 | GTAGTGTCAATGGAA[C/T]GGAGAGAAAAGGGTG | 137886 |
rs577201054 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58411381 | GCGCCGCTAGCCAGC[G/T]GAAGATGGCGGAGGG | 137886 |
rs577278272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424963 | AGAATATCAATCACA[A/G]CGTATGTCCCTGTCC | 137886 |
rs577391724 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412936 | CTTTCCCTGGCTAGT[C/G]AATTCTAATATCATT | 137886 |
rs577451563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413390 | TGTATCAAAAGTTTA[A/G]AAGAATTAAATAATG | 137886 |
rs577508310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446680 | ATGATAGCACATTTC[A/G]TAGTTTTAGACTCAC | 137886 |
rs577548006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431685 | TATATTCCCACATAT[A/G]TGAGAGAGCAAGTTT | 137886 |
rs577610540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425936 | AGAACAAAATCTCCA[A/G]GGTGGCTCTGGCTCT | 137886 |
rs577690391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431119 | ACTCACACCCACCCC[A/G]TCTCTCATGCCATCC | 137886 |
rs577797048 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433711 | GAGACTGAGGTGGGC[A/T]GATTGTTTGAGCCCA | 137886 |
rs577812083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444896 | TACTCTGAGAGAGAA[A/G]CTTTTTGAATGGAAG | 137886 |
rs577829776 | in-del | -/TA | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410669 | CAGCTAATTTTTGTG[-/TA]TATATATATATATAT | 137886 |
rs577833341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438850 | TTGGATGTTTTGTCC[C/T]CTCCAAATCTCATGT | 137886 |
rs577873035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440802 | AATATTGCTTCTTTA[C/T]GCTTTGCTATCTCTA | 137886 |
rs577875541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426431 | GCCAGGATGGTCTCA[A/G]TCTCCTGACTTTGTG | 137886 |
rs577936830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432921 | TATGATAATTTTGAC[A/G]TCCATTGTTGAGAAC | 137886 |
rs578039124 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424722 | TCCACTCGTCTGGTC[A/C/T]GCTAGAGAATACTTA | 137886 |
rs578047225 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448511 | AGATATGGTAAACAG[C/T]AACAATATTTTAAAA | 137886 |
rs578097643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426854 | ATCCTGGAGACTGTG[C/T]AGCCGCCCCCTAGGC | 137886 |
rs578143669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421883 | CTAAATGAAATCAAT[A/C]TAACAAACAAAGCTA | 137886 |
rs745374630 | snp | A/G | | | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435141 | CTAAGTAGATATGCA[A/G]CTAAAGACATAAAGT | 137886 |
rs745468618 | snp | A/G | 1.65655e-05 | 0.00287793 | missense, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439698 | TGGATATGGAGGATC[A/G]TCAGGATCAAGAATA | 137886 |
rs745506656 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417444 | TCTATGATTTTTGAA[A/G]TCTGTCTCTTCTTCC | 137886 |
rs745604064 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58415864 | GGGGTAAAAAAATTA[C/G]AAGTCTTTCATTTTG | 137886 |
rs745625650 | snp | A/C | 2.37894e-05 | 0.00344879 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434556 | AGTGGGACTTATTTT[A/C]TTAACAGACTACTCA | 137886 |
rs745787327 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440735 | CCCTTCAGTTGCCTC[A/G]TGTACACTGGTTGTC | 137886 |
rs745825157 | snp | A/C | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409851 | AGGCGTCAGCCACGA[A/C]GCCCAGCCTCAAATG | 137886 |
rs745914445 | snp | C/T | 3.45334e-05 | 0.00415518 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446082 | AGGTAAGCTTCTTTA[C/T]CAACAGTGTCCTGTT | 137886 |
rs745936707 | in-del | -/ATT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434369 | TATATATATATATAT[-/ATT]TTTTTTTTTTCTATA | 137886 |
rs746025228 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58430740 | ATTTTTCTATTATTT[A/G]CAAACATTGTTTTTC | 137886 |
rs746126720 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412118 | TTATCAGATACTAAC[A/G]CCACTTTTCTCATTT | 137886 |
rs746144657 | snp | A/G | 4.99729e-05 | 0.0049984 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58445954 | CTCCAGAAGAGGAGG[A/G]TAAATCAATACTTAA | 137886 |
rs746179998 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412592 | GTTCAGTAGTAGTAA[A/G]CAGTATCAAGGGATA | 137886 |
rs746314106 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411743 | AATGACATTTTGCGG[C/G]GTCAGTTGGTCGGTT | 137886 |
rs746358354 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422992 | TTAACTGCACCTCTA[C/T]TTCACACCCTTTTTT | 137886 |
rs746385268 | in-del | -/ATTGATG | 1.65952e-05 | 0.00288051 | frameshift-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58445983 | AATGCAGTTGTTCTT[-/ATTGATG]ATTCAGTGCCAACAA | 137886 |
rs746447162 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417338 | CAAAACAACTTTCAT[A/G]TGCAAGTTTGTCATT | 137886 |
rs746453190 | snp | C/T | 1.65935e-05 | 0.00288036 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433124 | TTTTGCTGAATAATC[C/T]TTTGTGAATTTTAAC | 137886 |
rs746468556 | snp | A/G | 1.65822e-05 | 0.00287938 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433137 | TCCTTTGTGAATTTT[A/G]ACTCACTTGCTATGT | 137886 |
rs746543587 | in-del | -/ATCT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431174 | GTTTTCATCTCTATA[-/ATCT]ATTTTATCATGTTAA | 137886 |
rs746576047 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58415038 | CTTTATATAATTCAA[C/T]GTCAATTTGTTGCCT | 137886 |
rs746598430 | in-del | -/TTC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436676 | ATGGTAATGAATGAG[-/TTC]TTCTTCTGGCAGTTC | 137886 |
rs746631544 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426670 | TATTTGGGTGAAACC[A/G]TCTCTACAATGTCAT | 137886 |
rs746655486 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423953 | AAAAAAAAAGCTACA[A/C]CTCTTAATTCATAAA | 137886 |
rs746753870 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425628 | TGTCTCAAATTCTTC[C/T]GAAAAGCCTTGTTTG | 137886 |
rs746769818 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440557 | TTTATAATACCCATG[A/G]CTTAATGTAATCTTA | 137886 |
rs746771324 | snp | A/T | 1.75075e-05 | 0.00295862 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439818 | TTGAACATGAATTTT[A/T]CTTTGAGAATAAGAA | 137886 |
rs746847614 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410181 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAT | 137886 |
rs746898748 | in-del | -/CATCA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423109 | CATCATCATCATCAT[-/CATCA]TCATCATCAATAGAG | 137886 |
rs747002448 | snp | C/G | 1.65715e-05 | 0.00287845 | missense, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439725 | AATACATAAAACCTA[C/G]ATTGAGGTTCAAGGC | 137886 |
rs747058482 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429305 | TCTGTGTTTGTCGTC[C/G]CTCCCTAAAATAATC | 137886 |
rs747062028 | snp | C/T | 1.67323e-05 | 0.00289239 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416941 | TCAAGAGCCCACGGA[C/T]ACCACCTCAACGGTA | 137886 |
rs747140993 | snp | A/G | 1.75835e-05 | 0.00296504 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446105 | GTCCTGTTTGCTGTT[A/G]TATACACTGGATTGC | 137886 |
rs747224553 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411661 | AACACAAGTGCCCAA[A/G]CCTCCAGCGCTGGTG | 137886 |
rs747275719 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422808 | ATTGGCAAAAATCAT[G/T]CAGGAAGCTTCTTGA | 137886 |
rs747276861 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432657 | AAAGTGCTGGGATTA[C/T]GAGCATGAGCCACCT | 137886 |
rs747296933 | snp | A/G | 1.67116e-05 | 0.0028906 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416859 | ATGTAGTTGGCCTTG[A/G]CAGAATTGTATGAAG | 137886 |
rs747314168 | snp | C/G | 4.97459e-05 | 0.00498703 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447407 | CCTGGATGTCCGGAA[C/G]TTTATTGTACAGTCT | 137886 |
rs747341323 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443122 | CAGGCCTGAGCTGCT[A/T]TCCTAAACCCCCTCC | 137886 |
rs747444065 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58435864 | AGGTAGTGGTTCTCA[G/T]CTATGTAAGACCCAT | 137886 |
rs747492824 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434681 | TATACTGCTATCTGT[A/G]TGTAAGTCACTGGTT | 137886 |
rs747493611 | snp | C/T | 6.62756e-05 | 0.00575616 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58433222 | GTCTGAATATATCTA[C/T]GGAGAAAATCAGCTG | 137886 |
rs747554733 | in-del | -/AAA | 4.04008e-05 | 0.0044943 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430691 | GCTCAATTTTAAACT[-/AAA]TACATTGTTTCTATA | 137886 |
rs747722271 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425512 | AGGACAACCCTGGTA[C/T]GATCAAAGGGCAGGT | 137886 |
rs747773601 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438676 | TCTTACAGGATTATA[A/G]GTAGAAAGAAGATGG | 137886 |
rs747791892 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450709 | GCACCTCAAGTACCT[A/G]GAAAACTCTTTTATG | 137886 |
rs747849299 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421419 | CCATGTGCCAGATAA[A/C]TCTTTCACCCCAAAA | 137886 |
rs747859190 | snp | G/T | 3.32878e-05 | 0.00407956 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433263 | GTACAATAATCAAAA[G/T]GAAAAAGTATAAATA | 137886 |
rs747885892 | in-del | -/C | 1.67075e-05 | 0.00289023 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447559 | TAAAATAATATTGTT[-/C]CTGTCCATGCAGTAG | 137886 |
rs747949374 | snp | C/T | 3.42448e-05 | 0.00413778 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416825 | TCCTAGTGTTATACT[C/T]TGTAACAAGCCTGTT | 137886 |
rs747981029 | snp | C/T | 1.70339e-05 | 0.00291833 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58445928 | ACCTGAAATAGTCAG[C/T]ACACCTTCCTCTCCA | 137886 |
rs747983711 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429523 | TTGTGGGGTTTAGTA[C/G]GGTTCTCCTGGTGTC | 137886 |
rs748201931 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442622 | ACATAGTACCCTCAC[A/T]TAATAGAAGAAAGCA | 137886 |
rs748284783 | snp | A/C/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409906 | ATGCCAAAGCTCGGG[A/C/T]GGCAAGCTGTCGACT | 137886 |
rs748324981 | snp | G/T | 1.65831e-05 | 0.00287945 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447497 | AACAGATGAAAGCCT[G/T]ACACTGCTAGAAGCA | 137886 |
rs748379377 | in-del | -/ATG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422580 | TTGGCTAAAACAAAA[-/ATG]ATCTCGTTCAACCTG | 137886 |
rs748438691 | in-del | -/ATGAAG | 1.66718e-05 | 0.00288715 | cds-indel, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416868 | CCTTGGCAGAATTGT[-/ATGAAG]ATGAAGATGAAGTGA | 137886 |
rs748474315 | snp | G/T | 0.000216705 | 0.010407 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430567 | AAATATAGTTCGACC[G/T]TCAACTGGGAAAATT | 137886 |
rs748523213 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449653 | AAAAGGAGCCATCAG[C/T]ACCAATCAATTTACA | 137886 |
rs748554121 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432658 | AAGTGCTGGGATTAC[C/G]AGCATGAGCCACCTC | 137886 |
rs748593500 | in-del | -/A | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58433017 | TTTTAGTCAAGTCTT[-/A]TGGTAATTTTGGTTC | 137886 |
rs748679129 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448427 | GATCCACCCACCTCA[A/G]CCTCCCAAAGTGCTG | 137886 |
rs748698412 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424564 | TCCACATCTATTTTT[A/G]TGCTGAAGTTTTGGC | 137886 |
rs748709215 | in-del | -/AG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442737 | GCCTAACAAAATCAC[-/AG]AGTCATTTTTAATAG | 137886 |
rs748742361 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414611 | TTTATCAATTTAAAT[G/T]ATCATTTCCTCTTTT | 137886 |
rs748754306 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438718 | GATGAGATTTTGGAC[-/T]TTTGAGTTAATGCTG | 137886 |
rs748755767 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437602 | TGCTGGGATTACAGG[C/T]GTAAGCCACCATGCC | 137886 |
rs748812933 | in-del | -/T | 0.00064168 | 0.0179005 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447349 | TACATGAAAATATGA[-/T]TTTTTTATATTACAA | 137886 |
rs748909762 | snp | G/T | 5.48933e-05 | 0.00523867 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434406 | AAAGGTTCAGATTTT[G/T]CTTAAACTGTGGAGC | 137886 |
rs748936727 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58444547 | TAGTGACGATGATAA[C/T]GTGTATACCTGGTTA | 137886 |
rs748958715 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436452 | TTATCACGTAAGACA[A/G]ATCTCCTGTTGCAGT | 137886 |
rs748987331 | in-del | -/T | 0.29131 | 0.246563 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434370 | ATATATATATATATA[-/T]TTTTTTTTTTTCTAT | 137886 |
rs749090350 | in-del | -/TATATATATATATATATATGTGTATA | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410669 | CAGCTAATTTTTGTG[-/TATATATATATATATATATGTGTATA]TATATGTATATATAT | 137886 |
rs749218750 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427998 | GGAGAGAGTTCAACT[A/G]TGAAACAGCGAAAGG | 137886 |
rs749233058 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426909 | TTTTTTTTTCTCTGT[C/T]TTCTAATAAGGTTTT | 137886 |
rs749331756 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58439217 | TATTTCCTTATAGCA[A/G]TGCAAATGGACTAGT | 137886 |
rs749348492 | in-del | -/TC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423096 | TCATCATCATCATCA[-/TC]ATCATCATCATCATC | 137886 |
rs749418561 | snp | C/G | 1.65921e-05 | 0.00288024 | missense, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439746 | GGTTCAAGGCTTTTA[C/G]TGGAGAAGGGCAAAA | 137886 |
rs749470479 | snp | A/G | 0.000135793 | 0.0082388 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430708 | ATACATTGTTTCTAT[A/G]TTTTACCTCCTCTTT | 137886 |
rs749493675 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419586 | GTCCTCCACAAGTCA[C/T]TGTATAGTAGTATTG | 137886 |
rs749636814 | snp | C/T | 1.67066e-05 | 0.00289016 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430594 | AATTGTGAATGAACT[C/T]TTCAAAGAGGCAAGG | 137886 |
rs749729038 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413744 | CTGGGAGCCCCCAGG[C/T]TACAAACTGCAGACT | 137886 |
rs749740408 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451330 | GCTTCATTGAGAGTC[-/A]TTTTCATGAATTATT | 137886 |
rs749749536 | snp | C/T | 4.97277e-05 | 0.00498612 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447423 | TTTATTGTACAGTCT[C/T]GTCCTGAATTTGCGG | 137886 |
rs749773019 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425463 | ATTTGCATTGATGTC[A/G]TCTGAAACAGGCTCG | 137886 |
rs749872201 | snp | A/G | 1.65927e-05 | 0.00288029 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447513 | ACACTGCTAGAAGCA[A/G]ATATTCTTAACACTG | 137886 |
rs749933224 | snp | G/T | 1.66139e-05 | 0.00288213 | stop-gained, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58446023 | AAATTCAAATCAGGT[G/T]AGCAGATGGGAGTCG | 137886 |
rs749959614 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417931 | CTTGCAAAATTGATA[A/G]CACCTTACAAAATTA | 137886 |
rs749986018 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428937 | AGTTCTTGTCCTCTA[C/G]CTTATACCACCTATA | 137886 |
rs750011478 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429994 | TTTACTTTTAACAAA[C/T]GCAGGGGCTTTTAAG | 137886 |
rs750161254 | in-del | -/CT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58435826 | GAGTTTTAGAAAAGA[-/CT]CTAAAGAAAATGAGT | 137886 |
rs750168437 | snp | A/T | 1.70796e-05 | 0.00292224 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439799 | AATGAGAAAAATACC[A/T]TTGTTGAACATGAAT | 137886 |
rs750179712 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411970 | AAAGCGATGCACTCT[A/G]TGCCCATACAGCCTA | 137886 |
rs750197220 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443872 | GTTTTTTAATACCAC[A/G]CTACCAGCTTGTCCA | 137886 |
rs750281670 | snp | A/G | | | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58411459 | GGCCTCCGAGCGCGC[A/G]GGATTTGCAGGTGAG | 137886 |
rs750313202 | snp | A/G | 8.34328e-05 | 0.00645828 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430558 | CAGTGGATTAAATAT[A/G]GTTCGACCTTCAACT | 137886 |
rs750328273 | snp | C/T | 5.09602e-05 | 0.00504752 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447602 | GATGATGTGCCGTAT[C/T]AATAAGGACAATACT | 137886 |
rs750334394 | in-del | -/AATT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443830 | TAAATAAATAAAATA[-/AATT]AATTAACATAACTTT | 137886 |
rs750393032 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422613 | GCTGGAGGCCTGTTA[C/G]GGCTGTTCCTTCTCA | 137886 |
rs750456109 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431943 | AATTGGATTATTTTG[C/T]TACTGTTGAGTTTTG | 137886 |
rs750614756 | snp | A/G | 8.52929e-05 | 0.00652987 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434462 | AATTGAGACCTTACA[A/G]TGAACCAACAAATGC | 137886 |
rs750706101 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426000 | CAGTTAATAATTTCT[C/G]TGCTTCTTTCCCAGA | 137886 |
rs750763219 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425235 | ACGCATGATGCCATA[C/T]TCTTTTAGAGCATAC | 137886 |
rs750820231 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438420 | ACCCATGAGAGAAGC[C/T]ACAGGGCCAGAGCTG | 137886 |
rs750856668 | snp | A/G | 1.73757e-05 | 0.00294747 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416799 | ACTTCTAGTTGTATG[A/G]AAGAGGTTATTCCTA | 137886 |
rs751010268 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58416016 | TAATCTGTTTTGTTA[C/T]GATTTTGGGTTTTTT | 137886 |
rs751014626 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428585 | TTAAGGCCCAGCTGA[G/T]TACTAATTCTGTACT | 137886 |
rs751127051 | snp | C/T | 3.3423e-05 | 0.00408783 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58446037 | TTAGCAGATGGGAGT[C/T]GTTTGATACAAAGAT | 137886 |
rs751148933 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443340 | TACATCCTTTCCTGC[C/T]ATTTGCCTACAAACC | 137886 |
rs751194735 | snp | A/C | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411217 | AACTCCCTTTAAGAA[A/C]AAAGGAGAAACCAAA | 137886 |
rs751232838 | snp | C/T | 1.86562e-05 | 0.00305414 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447357 | AAATATGATTTTTTA[C/T]ATTACAAATTATTTT | 137886 |
rs751247486 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422501 | TCGATGATTCAACAT[A/G]TAAGGCGAAGAGGGA | 137886 |
rs751266379 | snp | G/T | 1.72454e-05 | 0.00293639 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416816 | AGAGGTTATTCCTAG[G/T]GTTATACTTTGTAAC | 137886 |
rs751267195 | in-del | -/TC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58444083 | CCCCATCCTCCATTT[-/TC]TGTTTTGAGAAAAAG | 137886 |
rs751397162 | in-del | -/T | 0.000637552 | 0.0178429 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434363 | ATATATATATATATA[-/T]TATATATTTTTTTTT | 137886 |
rs751433099 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421427 | CAGATAACTCTTTCA[C/T]CCCAAAATATAAAAT | 137886 |
rs751470220 | snp | C/G | 1.65663e-05 | 0.002878 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58433187 | GGAGGATACAGATTG[C/G]GTAGTTCTTTTTGTA | 137886 |
rs751531612 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413219 | TGTAGGTTAGGGCAG[C/T]AGGAAGATAACTGAT | 137886 |
rs751542027 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445171 | CACTTTTGGCATATA[C/G]TGGCTGATCATCCTG | 137886 |
rs751562650 | snp | A/G | 0.000215508 | 0.0103782 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447470 | TGTGACTTCATTTCC[A/G]AATAAAGAGCTAACA | 137886 |
rs751592058 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421801 | CAACCTAGGGACTAT[A/G]ATAACTCTGGCCTTG | 137886 |
rs751650848 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425042 | TGCGTTCCTGCTTAT[A/G]GTGCACCTCCTCCAG | 137886 |
rs751705701 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412293 | CATCCATTGTAACAT[A/G]CTGCTGAGCTTTGCG | 137886 |
rs751725911 | in-del | -/TTT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434370 | ATATATATATATATA[-/TTT]TTTTTTTTTCTATAC | 137886 |
rs751802522 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438179 | GCTTTCGCATGGTGT[G/T]AAGCCTACAGGCACA | 137886 |
rs751930484 | in-del | -/C | 1.67892e-05 | 0.0028973 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439616 | AATGATAACTTTTTT[-/C]CCCCCCTTTTTAAAA | 137886 |
rs751934340 | snp | A/G | 1.88152e-05 | 0.00306712 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434508 | TGTTAAGAGAGGGTA[A/G]GATGTATTATTTGTA | 137886 |
rs751972989 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418804 | ATACTGTATTTTTAG[C/T]TGCTTCTTTAATTTG | 137886 |
rs752070104 | in-del | -/A | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422094 | TGCAATAAAAAGAAC[-/A]GGATTCAAGCTTCTT | 137886 |
rs752074547 | snp | A/T | 0.000328224 | 0.0128064 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434374 | ATATATATATATTTT[A/T]TTTTTTTCTATACCC | 137886 |
rs752095493 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446987 | GGTTTTAGTAGAGAC[A/G]GGGTTTTCACCGTGT | 137886 |
rs752143104 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441774 | GGAGAAACTGATGGA[A/C]GAAAGTGACAGAGAT | 137886 |
rs752219843 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413213 | ACTTGTTGTAGGTTA[G/T]GGCAGTAGGAAGATA | 137886 |
rs752267875 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440250 | ATTGTAAAGGGTTGT[C/T]GATGAGATAAAATAA | 137886 |
rs752404168 | snp | A/C | 1.83525e-05 | 0.00302918 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430485 | TTTATGTCTGTTATC[A/C]TAAGTTTTTATTCAT | 137886 |
rs752409715 | snp | A/T | 3.34303e-05 | 0.00408828 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447379 | AATTATTTTTGTCTT[A/T]TTTCTTCAGGATCCT | 137886 |
rs752417519 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421144 | CCCCAATAAAATTAC[C/G]TCTAAAAACAATCTT | 137886 |
rs752647335 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447927 | ATGCAGCATTGACCA[A/G]CAGCCATTAAGAAAT | 137886 |
rs752699987 | snp | C/T | 2.05413e-05 | 0.00320472 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430694 | CAATTTTAAACTAAA[C/T]ACATTGTTTCTATAT | 137886 |
rs752802333 | in-del | -/CAGA | 3.93461e-05 | 0.00443525 | frameshift-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434398 | TATACCCAAAAGGTT[-/CAGA]TTTTGCTTAAACTGT | 137886 |
rs753032506 | in-del | -/ATTA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420670 | ATAAACAGACAAATT[-/ATTA]ATTACATGATTTGAG | 137886 |
rs753078554 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427810 | TAGGAAGAGGTTATC[-/T]TTGGCAGTGGATAAA | 137886 |
rs753099064 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417685 | CCCATTATATCTTAT[A/T]CTCAGAAAGTCTATT | 137886 |
rs753107859 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428419 | TCATTATGTGTAATG[A/C]CATAATTGCATACAA | 137886 |
rs753125794 | in-del | -/AGTGGG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428299 | GTTGGGAACATTATC[-/AGTGGG]TAACCCCTATCACAA | 137886 |
rs753203604 | snp | A/C | 1.6727e-05 | 0.00289193 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439621 | ATAACTTTTTTCCCC[A/C]CTTTTTAAAAGAGAG | 137886 |
rs753342351 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438538 | AATGTCTGCCCTGCC[A/G]GGTTTCAGACTTCTG | 137886 |
rs753363288 | in-del | -/ATC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423082 | TGGTGAGACGAAATC[-/ATC]ATCATCATCATCATC | 137886 |
rs753364867 | snp | C/G | 1.65836e-05 | 0.0028795 | missense, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439648 | AGAGATTCCCCTGGA[C/G]CTTCAGCGCCTTGTT | 137886 |
rs753445797 | in-del | -/TTTG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58416030 | ATGATTTTGGGTTTT[-/TTTG]TTTGTTTGTTTTTTG | 137886 |
rs753486016 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58433846 | ATGGTATATTTTCAT[A/T]ATCTAAAATGAGGTG | 137886 |
rs753589432 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443636 | CATCTCTACTAAAAA[-/T]CCAAAAAAAAAAAAA | 137886 |
rs753601962 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418550 | CATGATTAGATTTTT[A/G]TTAGAATTTTTGTCG | 137886 |
rs753615556 | snp | A/G | 3.35587e-05 | 0.00409613 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430540 | CTCAAGTGAACATGA[A/G]TACAGTGGATTAAAT | 137886 |
rs753725039 | snp | C/T | 1.66076e-05 | 0.00288158 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447392 | TTATTTCTTCAGGAT[C/T]CTGGATGTCCGGAAC | 137886 |
rs753730482 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445065 | AGAAAAAACTTCAAG[A/T]CTATCAAAAATTCCT | 137886 |
rs753778325 | snp | G/T | 1.65787e-05 | 0.00287907 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447451 | CGGCTCTTGACTTTA[G/T]TCTTGTGACTTCATT | 137886 |
rs753787754 | in-del | -/CAAA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428698 | TAAATATTTTTGCCC[-/CAAA]CATTCATGAAGAATT | 137886 |
rs753808383 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58444188 | TAGAAAGAGCCCAAT[A/G]TAAACCTCAGCTCTC | 137886 |
rs753819344 | snp | A/C | 1.66302e-05 | 0.00288355 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416921 | TAGACCTAAAGCCAC[A/C]GTCTTCAAGAGCCCA | 137886 |
rs753859828 | snp | A/T | | | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435468 | CCTAGGAGGCAGTAT[A/T]TGGGGGTGGCAAATA | 137886 |
rs753880198 | in-del | -/ATA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434365 | TATATATATATATAT[-/ATA]TATTTTTTTTTTTTC | 137886 |
rs753936464 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450565 | TAGCATTAACATTCC[A/G]TATTTCTACTAACAG | 137886 |
rs754072056 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449427 | AAATCCAAAATCTTA[G/T]CTGAGTCTCACCAAC | 137886 |
rs754113852 | snp | A/G | 1.65669e-05 | 0.00287805 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58433200 | TGGGTAGTTCTTTTT[A/G]TAAGCGGTCTGAATA | 137886 |
rs754133195 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417189 | AAAAATTACCTTAAA[A/C]TACCTAATATTTTGG | 137886 |
rs754161829 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427249 | TGAAGCATTGCAGAT[C/T]GCTTGAGCTCACGAG | 137886 |
rs754187606 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414738 | CTCTAAATATTACTC[A/C]TTTTCTTCTAAGTTT | 137886 |
rs754211449 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426132 | GTTCTGTGTAATGCC[A/G]GACCAACTCAGCCAA | 137886 |
rs754235042 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423636 | GAGATGGGGTTTCAC[C/T]GTGTTAACCAGGATG | 137886 |
rs754256719 | snp | A/G | 1.70679e-05 | 0.00292124 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439796 | TAAAATGAGAAAAAT[A/G]CCTTTGTTGAACATG | 137886 |
rs754272683 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440097 | TTCATTTTGCAGATG[C/T]AGTAATTTGCCCAAG | 137886 |
rs754290090 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425727 | TCGTGTTAAGGGGCT[A/T]CGTGAGTTGTAGTAC | 137886 |
rs754311781 | snp | C/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409713 | TACAGGCACGCGCCA[C/T]CACGCCCAGCTAATT | 137886 |
rs754336959 | in-del | -/CAA | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448581 | ATTCATTTATTCATT[-/CAA]CAACACATTTTTCTA | 137886 |
rs754470490 | in-del | -/A | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443639 | CTCTACTAAAAATCC[-/A]AAAAAAAAAAAAAAA | 137886 |
rs754598212 | snp | C/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409774 | CACGTTGGCCAGGCT[C/G]GTCTGAAACTCCTGA | 137886 |
rs754663710 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420129 | TTAAAAGCTTTGACT[A/C]AAGATGGATACATCT | 137886 |
rs754675983 | snp | A/G | 1.71687e-05 | 0.00292986 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416822 | TATTCCTAGTGTTAT[A/G]CTTTGTAACAAGCCT | 137886 |
rs754692053 | snp | A/C | 2.23912e-05 | 0.0033459 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445862 | TGTCTTCAGTTTGTC[A/C]TATATTTTACACATT | 137886 |
rs754802024 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445103 | ACTGAGAAAATTGAG[C/T]TAAATTTATTTGAAT | 137886 |
rs754892915 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429075 | ATAAAAACCGTTAAC[C/T]GTAAAGGAGATAGGA | 137886 |
rs754989935 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429417 | AGCTTGGGACAAGGG[C/T]TTCCATAGGCTCCTG | 137886 |
rs754998249 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58444209 | CTCAGCTCTCTCACT[C/T]ACCAATAGGAATATT | 137886 |
rs755047392 | snp | C/G | 1.658e-05 | 0.00287919 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447486 | AATAAAGAGCTAACA[C/G]ATGAAAGCCTGACAC | 137886 |
rs755048909 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439729 | CATAAAACCTAGATT[A/G]AGGTTCAAGGCTTTT | 137886 |
rs755095183 | in-del | -/TATAT | 0.0138918 | 0.0821761 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434366 | ATATATATATATATA[-/TATAT]TTTTTTTTTTTCTAT | 137886 |
rs755100410 | snp | A/G | 1.66751e-05 | 0.00288744 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430563 | GATTAAATATAGTTC[A/G]ACCTTCAACTGGGAA | 137886 |
rs755171865 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442511 | TGTCTTCCATAGATG[G/T]CAGTCTAATTACACA | 137886 |
rs755216374 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449428 | AATCCAAAATCTTAT[C/G]TGAGTCTCACCAACT | 137886 |
rs755465194 | snp | C/T | 0.00122199 | 0.024688 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434382 | ATATTTTTTTTTTTT[C/T]TATACCCAAAAGGTT | 137886 |
rs755504095 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426512 | CGTGACCGGCCCAGT[G/T]TTCTGAATCTTGATG | 137886 |
rs755521667 | snp | A/G | 5.82756e-05 | 0.00539763 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434512 | AAGAGAGGGTAAGAT[A/G]TATTATTTGTATTCT | 137886 |
rs755525694 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440189 | TTTGTGCTTTTCACC[A/G]CTATATTATATGCCT | 137886 |
rs755594630 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418980 | TTCCTTGCTATTCAA[A/G]TATAATCATTAAGAT | 137886 |
rs755629780 | in-del | -/TTA | 1.75452e-05 | 0.00296181 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446102 | GTGTCCTGTTTGCTG[-/TTA]TTATATACACTGGAT | 137886 |
rs755752247 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428994 | TCTAAATATAGAAAT[A/T]AAAACAAATTTCTGG | 137886 |
rs755787721 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417949 | CCTTACAAAATTAAT[A/T]GTAATTCAGGCGGGG | 137886 |
rs755870619 | in-del | -/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442150 | AACAAGTGTATGTTT[-/G]TTTGGTGGAAGGGTA | 137886 |
rs755956050 | snp | A/C | 1.66073e-05 | 0.00288156 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416911 | CCAAGTCTAATAGAC[A/C]TAAAGCCACAGTCTT | 137886 |
rs756031240 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411496 | AGCCGGGGGAGGGAG[C/G]GCGGCGGTGGACGCG | 137886 |
rs756042687 | snp | G/T | 1.71064e-05 | 0.00292454 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416826 | CCTAGTGTTATACTT[G/T]GTAACAAGCCTGTTA | 137886 |
rs756083192 | snp | C/T | 1.66626e-05 | 0.00288635 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447384 | TTTTTGTCTTATTTC[C/T]TCAGGATCCTGGATG | 137886 |
rs756167679 | snp | C/T | 1.65666e-05 | 0.00287802 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58433197 | GATTGGGTAGTTCTT[C/T]TTGTAAGCGGTCTGA | 137886 |
rs756219221 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432026 | TGTAAATATTTTCTC[G/T]CAGAATGTCATTCAT | 137886 |
rs756272198 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448008 | TCTTTTGATTTTGAA[A/C]TTGTTTGATCATACA | 137886 |
rs756391513 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414697 | TAATGAACTCATGCC[A/G]TATGATGCCATATGG | 137886 |
rs756402220 | snp | C/T | 2.07872e-05 | 0.00322384 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430696 | ATTTTAAACTAAATA[C/T]ATTGTTTCTATATTT | 137886 |
rs756411381 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450337 | GAAATATCCTCAGCT[A/G]AATATTGAAGTCATC | 137886 |
rs756446494 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426080 | GGATATTTAAGCTCA[A/G]TAACATCTCCATTCT | 137886 |
rs756446603 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413563 | AGTCTTTCAGAGTGA[C/G]TAAAGGGGCAACATA | 137886 |
rs756504728 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421183 | TCTTGACTGTTTCCC[C/T]GAAGCAACTGGGCTC | 137886 |
rs756555031 | snp | C/G | 3.31697e-05 | 0.00407231 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447501 | GATGAAAGCCTGACA[C/G]TGCTAGAAGCAGATA | 137886 |
rs756569369 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425341 | TTTTCTTGGAATACC[A/G]TCCGCCAAAAGTCGT | 137886 |
rs756616649 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421342 | TGAAGCACCTTTTAG[-/T]TTTTTTTTTTTTTTA | 137886 |
rs756626516 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424487 | CAAGCCTTCCAAATC[C/T]AAATTTGGTCTTCAC | 137886 |
rs756637832 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437502 | CTGGCTAATTTTTGT[A/G]TTTAGTAGAGATGGG | 137886 |
rs756741413 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428592 | CCAGCTGAGTACTAA[C/T]TCTGTACTACAGATG | 137886 |
rs756784938 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417351 | ATGTGCAAGTTTGTC[A/G]TTCGTTTTTAAGGAT | 137886 |
rs756794820 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443439 | GGCTTGATCAATTGA[A/G]TGATAGGGAGAAAGT | 137886 |
rs756814104 | snp | C/T | 6.82314e-05 | 0.00584047 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439797 | AAAATGAGAAAAATA[C/T]CTTTGTTGAACATGA | 137886 |
rs756869190 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427452 | TGGGCAGTAGAGCCA[C/T]ATGTTGTCTCAAAAA | 137886 |
rs757019373 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409821 | TGCCTCGGCCTCCCA[A/G]AGAGTTGGGATTACA | 137886 |
rs757101493 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438788 | ATTGTATTTTGTGAT[A/G]TGAGAAGGACATGAG | 137886 |
rs757129979 | in-del | -/TATTT | 0.0337572 | 0.125455 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434368 | ATATATATATATATA[-/TATTT]TTTTTTTTTCTATAC | 137886 |
rs757141990 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421716 | CCTCTCTGCCTGATT[C/G]CATCCCATGTAAAGT | 137886 |
rs757232687 | snp | A/G | 1.67424e-05 | 0.00289326 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430544 | AGTGAACATGAATAC[A/G]GTGGATTAAATATAG | 137886 |
rs757234799 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58433815 | AAAATGAACAAATAT[A/G]TAGTTATTATTATAA | 137886 |
rs757270478 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420448 | AATAAACAGCATATT[A/G]TCAACATTTACATGA | 137886 |
rs757319351 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420928 | GGCATCCTGACATCA[C/G]GGAGGCCATGTGCTT | 137886 |
rs757376477 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413254 | TTATGAATGTGATTT[G/T]GTGTATCAAGTACAG | 137886 |
rs757388751 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445201 | GCTAGTGTTAGAAGG[G/T]GCTAAGACAGCAATG | 137886 |
rs757419272 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412524 | AGGCTGGAGAGATCA[C/G]TGTAACATTAGGAGG | 137886 |
rs757470614 | in-del | -/AT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434351 | TATGTATATGTGAAT[-/AT]ATATATATATATATA | 137886 |
rs757547826 | snp | C/T | 3.31329e-05 | 0.00407005 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58433201 | GGGTAGTTCTTTTTG[C/T]AAGCGGTCTGAATAT | 137886 |
rs757551842 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425083 | ACACCCCTGGGGTCA[A/G]TGGGCACTCCGTGGT | 137886 |
rs757590886 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424039 | AGCTTCTGACAGTCT[C/G]AGGCCCTAGCTTAAT | 137886 |
rs757630242 | in-del | -/AAAG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58447265 | GAAATACTATATATT[-/AAAG]AAAGTTACAACACCT | 137886 |
rs757660067 | in-del | -/TATATATT | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410785 | ATATATATATATATA[-/TATATATT]TTTTTTTTTAGTAGA | 137886 |
rs757705310 | snp | C/T | 1.65894e-05 | 0.00288 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430714 | TGTTTCTATATTTTA[C/T]CTCCTCTTTCATTTT | 137886 |
rs757719545 | in-del | -/A | 1.70151e-05 | 0.00291672 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439795 | TAAAATGAGAAAAAT[-/A]ACCTTTGTTGAACAT | 137886 |
rs757760997 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450943 | AAAATAAGCCCTACT[C/G]CTTTTCACTTACTGA | 137886 |
rs757804014 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411634 | TCGGGTCTTGACACT[C/G]TGGTGGTCGTGAACA | 137886 |
rs757809584 | in-del | -/TATT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434368 | ATATATATATATATA[-/TATT]TTTTTTTTTTCTATA | 137886 |
rs757921500 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426618 | CTGCTGTCAGCTCCT[C/G]TTATCAACAGTGGGT | 137886 |
rs758005516 | snp | C/T | 1.7303e-05 | 0.00294129 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416807 | TTGTATGGAAGAGGT[C/T]ATTCCTAGTGTTATA | 137886 |
rs758112865 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421172 | CTTGACCATTTTCTT[C/G]ACTGTTTCCCCGAAG | 137886 |
rs758114175 | snp | C/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409761 | GACAGGATTTCACCA[C/T]GTTGGCCAGGCTGGT | 137886 |
rs758261952 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431853 | CTAGTGATGAACATC[A/G]TTTCATGTGCTTCCT | 137886 |
rs758267886 | snp | A/G | 1.98399e-05 | 0.00314953 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430686 | TCAGTGCTCAATTTT[A/G]AACTAAATACATTGT | 137886 |
rs758273410 | snp | A/T | 3.31373e-05 | 0.00407032 | missense, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439715 | CAGGATCAAGAATAC[A/T]TAAAACCTAGATTGA | 137886 |
rs758379577 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447971 | AAGTTGAAAATTTGT[C/G]TATAATATATACTGA | 137886 |
rs758409742 | snp | A/G | | | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430643 | CTGAATGAAGCCACA[A/G]GAGCTTCAGGTGATG | 137886 |
rs758485943 | snp | C/T | 3.32055e-05 | 0.00407451 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447393 | TATTTCTTCAGGATC[C/T]TGGATGTCCGGAACT | 137886 |
rs758544376 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422742 | TCCCTAAACACATCC[A/G]TCCTCACAAGATCAG | 137886 |
rs758593081 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58435698 | ATTTATTGTTAAATG[A/T]AAATAAACCACAAAC | 137886 |
rs758608991 | in-del | -/A | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410778 | TATATATATATATAT[-/A]TATATATATATATTT | 137886 |
rs758621469 | in-del | -/A | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434367 | TATATATATATATAT[-/A]TATTTTTTTTTTTTC | 137886 |
rs758641422 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436987 | TTGCTCTAAAGATAC[A/G]TGAAGATGTGGAAGC | 137886 |
rs758643400 | in-del | -/TTG | 4.0744e-05 | 0.00451335 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434530 | TTATTTGTATTCTAT[-/TTG]TTATGTAGAGTGGGA | 137886 |
rs758648273 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428305 | AACATTATCAGTGGG[C/T]AACCCCTATCACAAT | 137886 |
rs758661277 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420692 | ACATGATTTGAGGCT[C/T]AGGATGAAAACTTGT | 137886 |
rs758703375 | snp | A/C/T | 0.000327879 | 0.0128003 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434373 | TATATATATATATTT[A/C/T]TTTTTTTTCTATACC | 137886 |
rs758725527 | in-del | -/CA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423109 | CATCATCATCATCAT[-/CA]TCATCATCATCAATA | 137886 |
rs758861756 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450781 | GGAATTCACCTTTCT[C/G]CAGGGTCACTGTTTA | 137886 |
rs758913419 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449667 | GCACCAATCAATTTA[C/T]AAAACCAGCGAGGCA | 137886 |
rs758921764 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417248 | TACTATTTTTCTTGG[A/G]CACAATGGTTCTTTA | 137886 |
rs758982364 | snp | C/T | 1.65679e-05 | 0.00287814 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58433209 | CTTTTTGTAAGCGGT[C/T]TGAATATATCTATGG | 137886 |
rs758999795 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442762 | TTAATAGGGAGGACT[A/G]GCGAGTAGGCATTCT | 137886 |
rs759064891 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422427 | ACAGCAAAGATGCCA[C/T]AGCATTTTATTACCA | 137886 |
rs759084719 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437391 | GGAGTGCAGTGGCGC[A/G]ATCTAGGCTCACTGC | 137886 |
rs759097339 | in-del | AGGCTGGAGTGCAGT/CACG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437371 | CATGCTCTGTCACCC[AGGCTGGAGTGCAGT/CACG]GGCGCGATCTAGGCT | 137886 |
rs759103069 | snp | G/T | 0.000144501 | 0.0084988 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447360 | TATGATTTTTTATAT[G/T]ACAAATTATTTTTGT | 137886 |
rs759146505 | snp | C/T | 1.84401e-05 | 0.0030364 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430477 | TACTTCAGTTTATGT[C/T]TGTTATCCTAAGTTT | 137886 |
rs759147581 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434283 | TAAATTAAGTAAATA[C/T]GTTTTAGGATATCAC | 137886 |
rs759150096 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449082 | ATGACCCTTCTGTTA[A/C]CACATCTCTCTGACA | 137886 |
rs759157228 | in-del | -/AT | 0.072888 | 0.176441 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434349 | CTTATGTATATGTGA[-/AT]ATATATATATATATA | 137886 |
rs759259105 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420388 | CTACATAATGTAAGT[C/G]GGCAAAAAGGCAATT | 137886 |
rs759298879 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431684 | TTATATTCCCACATA[C/T]ATGAGAGAGCAAGTT | 137886 |
rs759448831 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434363 | AATATATATATATAT[A/T]TATATATTTTTTTTT | 137886 |
rs759572349 | in-del | -/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434382 | ATATTTTTTTTTTTT[-/C]TATACCCAAAAGGTT | 137886 |
rs759684807 | snp | G/T | 1.68012e-05 | 0.00289833 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439778 | CTTGGAAGGTAAAAA[G/T]CCTAAAATGAGAAAA | 137886 |
rs759707937 | in-del | -/AGAG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437853 | GAGCAACCACTTGAT[-/AGAG]AGATTTGCATGAATA | 137886 |
rs759805168 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445500 | CCTTCATAACATAGT[A/G]TTATTCCCTCACTTT | 137886 |
rs759903730 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443026 | TGAAGCCTGACTGGG[A/T]TGTCAGCCCTGTGTG | 137886 |
rs759925669 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410362 | AGGCTGCAGTGAGCC[A/G]AGGTCGCGCCACTGC | 137886 |
rs760058063 | snp | C/G | 1.68224e-05 | 0.00290016 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430622 | AGGGAACATGGGGCT[C/G]TCCCTCTGAATGAAG | 137886 |
rs760177168 | snp | G/T | 1.7409e-05 | 0.00295029 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430514 | ATGAACTAAAATGTT[G/T]AAAGGTTTTACTCAA | 137886 |
rs760190391 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419973 | GACTCGATTTTCACT[G/T]TGCACTGGGTCTCAC | 137886 |
rs760219304 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432854 | GGCTTCAGGTATTAT[G/T]GTTCAATAAATTTGG | 137886 |
rs760253071 | snp | C/G | 1.67508e-05 | 0.00289398 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447564 | TAATATTGTTCCTGT[C/G]CATGCAGTAGCATGT | 137886 |
rs760272607 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431460 | ATATACCACAGTTTA[A/C]CCATTCATTTATTGA | 137886 |
rs760287603 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413957 | ACACACATGTTCATT[A/G]AGGTATTTAGTTGTA | 137886 |
rs760325162 | in-del | -/AAAAAAAAAA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418244 | GGACTCTGTCTCCAA[-/AAAAAAAAAA]AAAAAAAAAAAAATT | 137886 |
rs760456672 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445037 | GGAAACCATCTAAAT[A/C]TCAGAGTTCAAGAGA | 137886 |
rs760567430 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436975 | AGGAGTAGGGCATTG[A/C]TCTAAAGATACATGA | 137886 |
rs760590558 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423798 | TCAGCAACATTTGAC[A/G]ACCAAAAACACTGGT | 137886 |
rs760623995 | snp | C/T | 0.000185856 | 0.00963813 | intron-variant, missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434902 | TTCAGCAACTTATGT[C/T]AGAAATCTTTTAATG | 137886 |
rs760644108 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437860 | CACTTGATAGAGAGA[G/T]TTGCATGAATAGAAG | 137886 |
rs760700704 | in-del | -/GGGCTCTGATC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424696 | ACAAGGCGGGGGGGG[-/GGGCTCTGATC]TCCACTCGTCTGGTC | 137886 |
rs760941194 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427207 | AGGACGGTGGCTCAC[A/G]CCTGTCATCTTAGCA | 137886 |
rs760973282 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58439889 | CATGCACATTAGATA[C/T]ATACATCTGTTAATA | 137886 |
rs761010440 | snp | C/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409708 | GGGACTACAGGCACG[C/T]GCCACCACGCCCAGC | 137886 |
rs761068352 | in-del | -/TCC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413210 | CTACTTGTTGTAGGT[-/TCC]TAGGGCAGTAGGAAG | 137886 |
rs761121365 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414912 | AGAAAATTGTTATTT[A/G]ATTGGAAGCATTTAT | 137886 |
rs761132846 | snp | A/G | 1.69126e-05 | 0.00290792 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439788 | AAAAATCCTAAAATG[A/G]GAAAAATACCTTTGT | 137886 |
rs761451587 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412862 | TCCTACATTATCCTG[G/T]CTCAGTTGTTGCTGG | 137886 |
rs761525526 | in-del | -/TATA | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410670 | GCTAATTTTTGTGTA[-/TATA]TATATATATATATAT | 137886 |
rs761620503 | snp | C/G | 0.000111305 | 0.00745923 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430672 | TGATAAATCTAAGGT[C/G]AGTGCTCAATTTTAA | 137886 |
rs761682494 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422542 | AAAGGCACTTAAGGT[A/G]GAACATTAGCAAATC | 137886 |
rs761708254 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441831 | ACTAGCCATATTGAT[C/T]AAGATTTTGATTATG | 137886 |
rs761738895 | snp | A/G | | | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435413 | GGCAACAAATGCCCT[A/G]AGAAGTATGCTGAAG | 137886 |
rs761738938 | snp | A/G | | | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451612 | TGGCGCACCTTTGTC[A/G]GGGACAGGGAAGGAA | 137886 |
rs761762385 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414396 | GAATTCCAATACTTT[C/T]AATATTTTGCTATAT | 137886 |
rs761779891 | snp | C/T | 0.000101781 | 0.00713304 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447597 | GAATAGATGATGTGC[C/T]GTATTAATAAGGACA | 137886 |
rs761790191 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450552 | TTCAAGGCCGCCCTA[C/G]CATTAACATTCCATA | 137886 |
rs761792957 | in-del | -/A | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434365 | TATATATATATATAT[-/A]TATATTTTTTTTTTT | 137886 |
rs761948980 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426779 | CGAGGGAGGCCCGCT[C/T]GGGACCAGATGCGGG | 137886 |
rs761992409 | snp | C/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409615 | ACCCAGGCTGAAGTG[C/T]AATGGTGCATCTCTG | 137886 |
rs762014537 | snp | A/C | 3.40078e-05 | 0.00412344 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434455 | GATGGAGAATTGAGA[A/C]CTTACAATGAACCAA | 137886 |
rs762170770 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419797 | GAACTTTAGTAGCTT[A/C]GTAGCAAATAAGGTT | 137886 |
rs762177824 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438199 | CTACAGGCACACAGA[A/T]TGCACAAGTGAAAGA | 137886 |
rs762216488 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431205 | GAGTGTTAAACCAGC[C/T]GGGTGTGGTGGCTCA | 137886 |
rs762222616 | snp | A/C | 1.65968e-05 | 0.00288065 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58446015 | AACAACAAAAATTCA[A/C]ATCAGGTTAGCAGAT | 137886 |
rs762269464 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446272 | ATTTAAACAGTCTCT[A/G]TAAACTATCCAAATA | 137886 |
rs762270373 | snp | A/G | 1.66496e-05 | 0.00288522 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416877 | GAATTGTATGAAGAT[A/G]AAGTGAAGTGCAAAT | 137886 |
rs762277737 | snp | G/T | 0.000117213 | 0.00765458 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58411469 | CGCGCGGGATTTGCA[G/T]GTGAGGCGAGGAGCC | 137886 |
rs762295511 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418826 | TTTAATTTGTATATT[C/T]TCCCAAGTCTTGAAA | 137886 |
rs762423632 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429921 | ATGTTTCCTAGGACC[A/G]TTTATGAAGTTGGAG | 137886 |
rs762432081 | snp | A/T | 3.53376e-05 | 0.00420328 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446111 | TTTGCTGTTATATAC[A/T]CTGGATTGCTTATCT | 137886 |
rs762502531 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422440 | CACAGCATTTTATTA[C/T]CATCACAAAAGTCAA | 137886 |
rs762506712 | in-del | -/TC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58415429 | GTATGTGCATGTCTG[-/TC]TCTCTCTCTCCTCTA | 137886 |
rs762534006 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423107 | ATCATCATCATCATC[A/G]TCATCATCATCATCA | 137886 |
rs762534207 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413214 | CTTGTTGTAGGTTAG[G/T]GCAGTAGGAAGATAA | 137886 |
rs762560162 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410946 | CCAAGCACTTTTTAC[A/G]GTGTTTTTCACTCTC | 137886 |
rs762576272 | snp | A/G | 3.92434e-05 | 0.00442946 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447340 | GTTTTAAGTTTACAT[A/G]AAAATATGATTTTTT | 137886 |
rs762620331 | in-del | -/ATATAT | 0.00838911 | 0.0642198 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434349 | CTTATGTATATGTGA[-/ATATAT]ATATATATATATATA | 137886 |
rs762691921 | snp | A/G | 1.67998e-05 | 0.00289821 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433295 | TTGCTTCTAGTTACT[A/G]AAACTGTTGGTTTTA | 137886 |
rs762737340 | snp | A/G | 1.66294e-05 | 0.00288347 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58446027 | TCAAATCAGGTTAGC[A/G]GATGGGAGTCGTTTG | 137886 |
rs762786377 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422517 | TAAGGCGAAGAGGGA[C/T]GTCTTTGGAAAAGGC | 137886 |
rs762811465 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449313 | TTCCCACCCACCCCC[C/T]GCTCCACTCCTGTGT | 137886 |
rs762844934 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424502 | CAAATTTGGTCTTCA[C/T]ATAAACTTTCTTGCG | 137886 |
rs762954128 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438156 | AGCCACTACTGTAAG[C/T]CTTGGTGGCTTTCGC | 137886 |
rs762998772 | snp | G/T | 1.6569e-05 | 0.00287824 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433152 | AACTCACTTGCTATG[G/T]ATTTTAGTCATTTAC | 137886 |
rs763185391 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449495 | TAAGTTTGGGAGAGG[A/G]TCTGTGTGTGATTTC | 137886 |
rs763204675 | snp | A/T | | | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451869 | TCTCTGCTCACTGAG[A/T]TAAAGGCCTGTCTGA | 137886 |
rs763233939 | snp | G/T | 5.11793e-05 | 0.00505836 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434463 | ATTGAGACCTTACAA[G/T]GAACCAACAAATGCT | 137886 |
rs763337611 | in-del | -/TT | 0.000977072 | 0.0220812 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433154 | CTCACTTGCTATGTA[-/TT]TTAGTCATTTACAGG | 137886 |
rs763491800 | snp | A/G | 1.65971e-05 | 0.00288067 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416887 | AAGATGAAGTGAAGT[A/G]CAAATCTTCCAAGTC | 137886 |
rs763566582 | snp | C/T | 8.33299e-05 | 0.0064543 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439627 | TTTTTCCCCCCTTTT[C/T]AAAAGAGAGATTCCC | 137886 |
rs763582698 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441467 | TATTTATTGAGATTA[C/T]GATTTTTAATTAGAA | 137886 |
rs763615732 | snp | A/G | 1.70787e-05 | 0.00292217 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416953 | GGACACCACCTCAAC[A/G]GTAAGTTTTATTTTG | 137886 |
rs763630701 | snp | A/G | 8.93471e-05 | 0.00668323 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430663 | TTCAGGTGATGATAA[A/G]TCTAAGGTCAGTGCT | 137886 |
rs763698628 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58415616 | GGAACACATGCTTTG[-/T]GCTTTCCATACATTA | 137886 |
rs763762085 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441880 | CTGGTAGTAATAGGT[G/T]TCTTACAGGATCTTG | 137886 |
rs763817682 | snp | C/T | 3.31565e-05 | 0.0040715 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447449 | TGCGGCTCTTGACTT[C/T]ATTCTTGTGACTTCA | 137886 |
rs763877497 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422490 | AATATCCACACTCGA[C/T]GATTCAACATATAAG | 137886 |
rs763900877 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58433501 | AATTTGCAGCCAGGC[A/G]TGGTGACATGCATCT | 137886 |
rs763910565 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409762 | ACAGGATTTCACCAC[A/G]TTGGCCAGGCTGGTC | 137886 |
rs763942670 | snp | A/G | 3.35739e-05 | 0.00409705 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447574 | CCTGTCCATGCAGTA[A/G]CATGTGGGAATAGAT | 137886 |
rs763957129 | in-del | -/A | 0.000696136 | 0.0186436 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434363 | AATATATATATATAT[-/A]TATATATTTTTTTTT | 137886 |
rs763981114 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450510 | ATATTCTATGGCAAT[C/T]GAGGTATTCTCTATT | 137886 |
rs764016559 | snp | A/G | 1.68641e-05 | 0.00290375 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430533 | GGTTTTACTCAAGTG[A/G]ACATGAATACAGTGG | 137886 |
rs764184846 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58416297 | GTATAATTTGGTAAT[A/G]TTACTTTCTAAATGG | 137886 |
rs764199726 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425006 | CACTGCCGTGCACCA[C/T]GACTGGCCTTGCATG | 137886 |
rs764207300 | snp | C/T | 1.65666e-05 | 0.00287802 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58433199 | TTGGGTAGTTCTTTT[C/T]GTAAGCGGTCTGAAT | 137886 |
rs764232208 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449780 | TTACTTTTTCACAAA[A/T]GGTAGCACACGTTTG | 137886 |
rs764333726 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434366 | ATATATATATATATA[C/T]ATATTTTTTTTTTTT | 137886 |
rs764354385 | in-del | -/ATATATATA | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410780 | TATATATATATATAT[-/ATATATATA]TATTTTTTTTTTTAG | 137886 |
rs764473567 | in-del | -/ACA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423113 | TCATCATCATCATCA[-/ACA]TCATCATCAATAGAG | 137886 |
rs764630623 | snp | A/G | 1.69922e-05 | 0.00291476 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439794 | CCTAAAATGAGAAAA[A/G]TACCTTTGTTGAACA | 137886 |
rs764720765 | in-del | -/TA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58416426 | CTTCTGAAATTGTTT[-/TA]TATGCTTGGAGTTTG | 137886 |
rs764872927 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439712 | CATCAGGATCAAGAA[A/T]ACATAAAACCTAGAT | 137886 |
rs764898139 | snp | C/G | 1.66076e-05 | 0.00288158 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58446020 | CAAAAATTCAAATCA[C/G]GTTAGCAGATGGGAG | 137886 |
rs764922566 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421071 | ACACTTCACAATTGC[A/T]AACCTTTCCACATCC | 137886 |
rs764954680 | snp | A/C | 3.86802e-05 | 0.00439757 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430680 | CTAAGGTCAGTGCTC[A/C]ATTTTAAACTAAATA | 137886 |
rs764961178 | in-del | -/CT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424598 | TTTTCTCATCTGAAA[-/CT]CTTCTGCTGTTGCAT | 137886 |
rs765005760 | snp | C/T | 1.65671e-05 | 0.00287807 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58433205 | AGTTCTTTTTGTAAG[C/T]GGTCTGAATATATCT | 137886 |
rs765010492 | in-del | -/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413212 | ACTTGTTGTAGGTTA[-/C]GGGCAGTAGGAAGAT | 137886 |
rs765031691 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414275 | CCCAGAGTGTGATTC[A/T]TTGGTTCTAGAGTAG | 137886 |
rs765044081 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447723 | AAATTTGGATTAGGA[A/G]TAGACCTTGAGATAA | 137886 |
rs765086749 | snp | C/T | 1.65707e-05 | 0.00287838 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433148 | TTTTAACTCACTTGC[C/T]ATGTATTTTAGTCAT | 137886 |
rs765156815 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425728 | CGTGTTAAGGGGCTA[C/T]GTGAGTTGTAGTACT | 137886 |
rs765273690 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413212 | TACTTGTTGTAGGTT[A/G]GGGCAGTAGGAAGAT | 137886 |
rs765303281 | in-del | -/CTATACCCAAAAGGTTCAGA | 0.000100822 | 0.00709934 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434382 | ATATTTTTTTTTTTT[-/CTATACCCAAAAGGTTCAGA]TTTTGCTTAAACTGT | 137886 |
rs765333042 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436984 | GCATTGCTCTAAAGA[G/T]ACATGAAGATGTGGA | 137886 |
rs765334345 | snp | A/G | | | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435594 | GCTAAGCGAAAACCA[A/G]CATAACTGTAGAAAT | 137886 |
rs765387490 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450723 | TAGAAAACTCTTTTA[C/T]GCCTGCTTCTCTGCC | 137886 |
rs765393348 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434365 | ATATATATATATATA[-/T]TATATTTTTTTTTTT | 137886 |
rs765431556 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417664 | TGGGGAAGAAACGTC[A/G]GTTTTCCCATTATAT | 137886 |
rs765532229 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413768 | GCAGACTCGGAAATG[-/T]TTTTTTGCATATCAG | 137886 |
rs765554998 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428283 | GCTCAACTCTTCTGA[A/C]GTTGGGAACATTATC | 137886 |
rs765564890 | in-del | -/AT | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449368 | AAATTTACATCACTC[-/AT]AGGTGCTCAAAAGTC | 137886 |
rs765604752 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417097 | TCGAGGCAGATTTGG[A/G]TAAAAAATAGAAATG | 137886 |
rs765657737 | in-del | -/TCC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443635 | CATCTCTACTAAAAA[-/TCC]TCCAAAAAAAAAAAA | 137886 |
rs765682016 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443082 | AGCTGTGCTGAGCAG[C/G]CAGTGCTGTGCCTCG | 137886 |
rs765721899 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427344 | GGTGCACGCCTGTAG[C/T]CCCAACTGCTCGGGA | 137886 |
rs765735038 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441728 | AGTCATTTTCCTTAT[A/T]AGGCAAATAGAGAAA | 137886 |
rs765773427 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420003 | CAAATTATGTAGCCA[A/G]TTGCGGATACAGCCT | 137886 |
rs765823417 | in-del | -/GTC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423097 | ATCATCATCATCATC[-/GTC]ATCATCATCATCATC | 137886 |
rs765906756 | snp | A/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410375 | CCGAGGTCGCGCCAC[A/T]GCACTCCAGCTTGGG | 137886 |
rs765918842 | in-del | -/TACTC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425276 | AGTATTTGACACATT[-/TACTC]TATCCTCTCTCCACT | 137886 |
rs765933539 | snp | A/C | 1.72785e-05 | 0.00293921 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416814 | GAAGAGGTTATTCCT[A/C]GTGTTATACTTTGTA | 137886 |
rs766056901 | snp | C/G/T | 4.98023e-05 | 0.0049899 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416897 | GAAGTGCAAATCTTC[C/G/T]AAGTCTAATAGACCT | 137886 |
rs766130436 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58447074 | AAAGTGCTGGAATTA[C/T]AGGCGTAAGCCACCG | 137886 |
rs766145751 | snp | C/T | 0.000228193 | 0.0106792 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434344 | ATATTCTTATGTATA[C/T]GTGAATATATATATA | 137886 |
rs766189353 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445433 | CAATAGCTGGCACCC[A/G]TTGAAACACTGTGTT | 137886 |
rs766189791 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413045 | AGCTTGCTTAATGAC[A/C]ACCTGATTCTTGGCA | 137886 |
rs766198632 | snp | C/T | 4.97022e-05 | 0.00498484 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58433161 | GCTATGTATTTTAGT[C/T]ATTTACAGGTGGAGG | 137886 |
rs766242851 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424931 | AGTCAACACCTTTCT[C/T]TCTGTTGATGTCAGT | 137886 |
rs766262102 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420324 | CTAATGTTTCTCTAC[A/G]TAAAGTATTCTTTTA | 137886 |
rs766266743 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445062 | AAGAGAAAAAACTTC[A/G]AGACTATCAAAAATT | 137886 |
rs766369747 | snp | A/C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423871 | AATGCAAAGAAAATA[A/C/T]GGCAAACGTTTTCCC | 137886 |
rs766521938 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442154 | AGTGTATGTTTGTTT[G/T]GTGGAAGGGTAGAAT | 137886 |
rs766530496 | snp | C/T | 4.97368e-05 | 0.00498657 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447469 | TTGTGACTTCATTTC[C/T]GAATAAAGAGCTAAC | 137886 |
rs766596014 | snp | G/T | 1.69438e-05 | 0.00291061 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439592 | GTGTAGTTTAATTCT[G/T]GGAAAACTTAATGAT | 137886 |
rs766713981 | snp | C/T | 1.88064e-05 | 0.0030664 | splice-donor-variant | UBXN2B | GRCh38.p7 | 8:58434506 | TCTGTTAAGAGAGGG[C/T]AAGATGTATTATTTG | 137886 |
rs766841202 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409709 | GGACTACAGGCACGC[A/G]CCACCACGCCCAGCT | 137886 |
rs766879377 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425713 | AACATTTATACGAGT[C/T]GTGTTAAGGGGCTAC | 137886 |
rs766884769 | snp | C/T | 1.83737e-05 | 0.00303093 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430481 | TCAGTTTATGTCTGT[C/T]ATCCTAAGTTTTTAT | 137886 |
rs767158332 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428739 | AGGACTTACACTGCT[G/T]CATGCAAAGACTTAT | 137886 |
rs767203105 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428664 | TTGAATGAGTATAGA[A/G]AATTACTTCAGCAAT | 137886 |
rs767241623 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445003 | TGCGTGTCTTTCTTC[C/T]AGAAGAAAATAATCT | 137886 |
rs767394515 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422583 | GCTAAAACAAAAATG[A/T]TCTCGTTCAACCTGG | 137886 |
rs767399545 | snp | A/G | 1.68289e-05 | 0.00290072 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447374 | TTACAAATTATTTTT[A/G]TCTTATTTCTTCAGG | 137886 |
rs767447528 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58416189 | AAATTCTATACAATA[A/C]TGAAATATTGGATTA | 137886 |
rs767544864 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425476 | TCATCTGAAACAGGC[C/T]CGTTGGGATCACCAT | 137886 |
rs767570184 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447979 | AATTTGTCTATAATA[A/T]ATACTGAAACGTGTC | 137886 |
rs767630585 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423270 | CTGAAAGAGACTACA[C/G]GAAGAAGGAGAGACT | 137886 |
rs767697993 | snp | A/G | 2.00022e-05 | 0.00316239 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430688 | AGTGCTCAATTTTAA[A/G]CTAAATACATTGTTT | 137886 |
rs767976668 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418877 | TACTTGCATTTTACT[C/T]ACTATTTGGCCACTG | 137886 |
rs767984017 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411356 | GTTGCGGCAGGTGCG[C/T]CCGCAGCGGGCGCCG | 137886 |
rs768013007 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419865 | CATGTGACCTGTGCT[A/G]TTGCACAAGGCCCCA | 137886 |
rs768136139 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423148 | GTAGAAGGGAAGCTG[C/T]GACAATTCTGGACTT | 137886 |
rs768159329 | snp | A/G | 3.31614e-05 | 0.00407181 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58433239 | GAGAAAATCAGCTGC[A/G]AGATGTAGGTACAAT | 137886 |
rs768164541 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58433141 | TTGTGAATTTTAACT[C/T]ACTTGCTATGTATTT | 137886 |
rs768215746 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417738 | AAAGCAAGACTAGTA[A/G]AGTAAATACTGTGTT | 137886 |
rs768246047 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424637 | ACGTTTTCATACACT[C/G]TAGCACTGTCTGCTC | 137886 |
rs768321689 | in-del | -/AC | 1.65789e-05 | 0.0028791 | frameshift-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447416 | CCGGAACTTTATTGT[-/AC]AGTCTCGTCCTGAAT | 137886 |
rs768328724 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447822 | TGTTACATGCTTAGT[A/G]TTAATGTAACAACAT | 137886 |
rs768391987 | in-del | -/CA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423112 | CATCATCATCATCAT[-/CA]TCATCATCAATAGAG | 137886 |
rs768420764 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451395 | CTCAAAAAAGATGTC[A/G]CAATGAACAGACAAC | 137886 |
rs768556770 | snp | C/T | 8.81998e-05 | 0.00664019 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446108 | CTGTTTGCTGTTATA[C/T]ACACTGGATTGCTTA | 137886 |
rs768558077 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424652 | CTAGCACTGTCTGCT[C/G]TCATTTCTGCACAGC | 137886 |
rs768617980 | snp | A/G | 1.65721e-05 | 0.0028785 | synonymous-codon, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439726 | ATACATAAAACCTAG[A/G]TTGAGGTTCAAGGCT | 137886 |
rs768642930 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409297 | GGAAAATAAACACCC[A/G]AAGAAGTGGCTAGGC | 137886 |
rs768684921 | snp | C/G | 1.6777e-05 | 0.00289624 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416943 | AAGAGCCCACGGACA[C/G]CACCTCAACGGTAAG | 137886 |
rs768739332 | snp | G/T | 4.97368e-05 | 0.00498657 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447413 | TGTCCGGAACTTTAT[G/T]GTACAGTCTCGTCCT | 137886 |
rs768799670 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420542 | AAATATCTTTTAATA[C/T]TCTGGTACTTCATAT | 137886 |
rs768850765 | snp | A/C | 5.0119e-05 | 0.0050057 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416860 | TGTAGTTGGCCTTGG[A/C]AGAATTGTATGAAGA | 137886 |
rs768851160 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414287 | TTCATTGGTTCTAGA[A/G]TAGAGTTTAAGCATA | 137886 |
rs768853683 | snp | A/C | 1.66081e-05 | 0.00288163 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58445968 | GATAAATCAATACTT[A/C]ATGCAGTTGTTCTTA | 137886 |
rs768928409 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432487 | TCCCGGGTTCACACC[A/G]TTCTCCTGCCTCAGC | 137886 |
rs768996763 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445866 | TTCAGTTTGTCATAT[A/G]TTTTACACATTCAGA | 137886 |
rs769039776 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413748 | GAGCCCCCAGGTTAC[A/G]AACTGCAGACTCGGA | 137886 |
rs769069675 | snp | C/T | 1.65553e-05 | 0.00287705 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446106 | TCCTGTTTGCTGTTA[C/T]ATACACTGGATTGCT | 137886 |
rs769255732 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412823 | GTAAGGATTAAATAA[C/T]GTTATAAAGGGCCTA | 137886 |
rs769257504 | snp | A/G | 2.15799e-05 | 0.00328473 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434391 | TTTTTTCTATACCCA[A/G]AAGGTTCAGATTTTG | 137886 |
rs769270879 | snp | A/G | | | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435152 | TGCAACTAAAGACAT[A/G]AAGTTGAGCATAAAC | 137886 |
rs769319066 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436370 | GTTAGGTTTTAGGAT[A/C]AGACAGTATTATCCA | 137886 |
rs769366580 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440611 | AGTTACCCTCTACTC[A/G]TCCACATATTGTTGC | 137886 |
rs769399415 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450152 | TAAAGGCTGTCCTGA[C/T]GGTGAATCTTAGTTT | 137886 |
rs769416798 | snp | A/G | 3.33023e-05 | 0.00408044 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433269 | TAATCAAAATGAAAA[A/G]GTATAAATATTTGCT | 137886 |
rs769457309 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422435 | GATGCCACAGCATTT[G/T]ATTACCATCACAAAA | 137886 |
rs769463462 | in-del | -/A | 0.0389115 | 0.133946 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434369 | TATATATATATATAT[-/A]TTTTTTTTTTTTCTA | 137886 |
rs769507881 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427819 | GTTATCTTTGGCAGT[C/G]GATAAATATTTTGAT | 137886 |
rs769666550 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58415942 | ATTAACATTGCCCCA[A/G]TGCCCTGTTCTTCTT | 137886 |
rs769704444 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58433047 | CTTGAAGGCTCCCCA[A/G]TATGAGCCACTTTGG | 137886 |
rs769755422 | snp | G/T | 0.118726 | 0.212761 | utr-variant-5-prime, upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411352 | GGAAGTTGCGGCAGG[G/T]GCGTCCGCAGCGGGC | 137886 |
rs769780484 | in-del | -/A | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412949 | GTCAATTCTAATATC[-/A]TTAAAGTTAATAGAG | 137886 |
rs769787157 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425345 | CTTGGAATACCATCC[G/T]CCAAAAGTCGTTCAC | 137886 |
rs769798926 | snp | A/C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419567 | ACAATCAGAACTTGG[A/C/G]TATGTCCTCCACAAG | 137886 |
rs769871853 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424083 | AAAATAGAAGCCATC[A/G]AAATGAATTATCCAC | 137886 |
rs769897142 | snp | A/T | 1.6681e-05 | 0.00288794 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430587 | CTGGGAAAATTGTGA[A/T]TGAACTTTTCAAAGA | 137886 |
rs769948099 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58430892 | ATTACAAAATAATTA[C/G]TAGAGTCACAGGCAT | 137886 |
rs769982663 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436169 | CAGAAAAATGAAGTA[C/T]ATGAGGTTGTCAGCT | 137886 |
rs770058951 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429556 | CTTGTTCTCCATCCT[A/G]ATGGATCTTTTCCTT | 137886 |
rs770069364 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445544 | CTGGGATTCAAAATG[A/G]TTGATGTACTTACTC | 137886 |
rs770112500 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58444735 | AGAAATTCCTTAATA[C/T]CTGATCATTTATTGT | 137886 |
rs770203167 | snp | A/G | 1.69714e-05 | 0.00291298 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416950 | CACGGACACCACCTC[A/G]ACGGTAAGTTTTATT | 137886 |
rs770238296 | snp | C/G | 1.65773e-05 | 0.00287895 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447419 | GAACTTTATTGTACA[C/G]TCTCGTCCTGAATTT | 137886 |
rs770394084 | snp | G/T | 1.77874e-05 | 0.00298218 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446119 | TATATACACTGGATT[G/T]CTTATCTAAGTAGAA | 137886 |
rs770411382 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423973 | TAATTCATAAATATC[C/T]ATGATTCCTTTTCTA | 137886 |
rs770529022 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432884 | GGATATGCCTAGAAA[C/T]GTGTCTTTTTAAAAA | 137886 |
rs770601659 | snp | C/G | 4.53402e-05 | 0.0047611 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434548 | TTATGTAGAGTGGGA[C/G]TTATTTTCTTAACAG | 137886 |
rs770634111 | snp | A/G | 3.46392e-05 | 0.00416154 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434420 | TGCTTAAACTGTGGA[A/G]CAATGGTTTCAGTTT | 137886 |
rs770636977 | snp | A/G/T | 3.315e-05 | 0.00407113 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447424 | TTATTGTACAGTCTC[A/G/T]TCCTGAATTTGCGGC | 137886 |
rs770655465 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448670 | CAGAACAAGACTAGT[G/T]TAGAAATACAGGAAT | 137886 |
rs770787818 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425629 | GTCTCAAATTCTTCC[G/T]AAAAGCCTTGTTTGA | 137886 |
rs770840274 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438024 | GGCCAAACTTGGGGC[C/T]CAGCTGCCCTGTGCA | 137886 |
rs770871211 | snp | G/T | 1.66211e-05 | 0.00288275 | synonymous-codon, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439756 | TTTTAGTGGAGAAGG[G/T]CAAAAACTTGGAAGG | 137886 |
rs771043437 | snp | C/T | 1.67956e-05 | 0.00289784 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58445939 | TCAGTACACCTTCCT[C/T]TCCAGAAGAGGAGGA | 137886 |
rs771123084 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428054 | TCAAATGTTTCAGAA[A/C]GTGTTTAATAACTGA | 137886 |
rs771220999 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411698 | CTCCCTTCCACCCCA[C/T]GTATGATGTAAAAAT | 137886 |
rs771247622 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442844 | TGATGTTTCTGCAGA[A/G]GAACAGTCACTGCCT | 137886 |
rs771272149 | in-del | -/AG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443469 | TTTTAAATAGCAAAC[-/AG]ATGTGATTTTGACAG | 137886 |
rs771360882 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58415039 | TTTATATAATTCAAC[A/G]TCAATTTGTTGCCTT | 137886 |
rs771544819 | snp | A/T | 4.09819e-05 | 0.00452651 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416990 | TGTAAAAAGAAATTA[A/T]AATCCTTTCTAAAAA | 137886 |
rs771560356 | snp | G/T | 1.66788e-05 | 0.00288775 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447552 | CAGCAACTAAAATAA[G/T]ATTGTTCCTGTCCAT | 137886 |
rs771622460 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434755 | AAATCTGATGAAACT[A/G]TGAACCCAGCTCCAA | 137886 |
rs771626161 | in-del | -/ACTT | 1.65791e-05 | 0.00287911 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433142 | TGTGAATTTTAACTC[-/ACTT]GCTATGTATTTTAGT | 137886 |
rs771632202 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413911 | ATAGTATTTCTGAAT[C/T]GCTTTCTCTTCTGGT | 137886 |
rs771645273 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425520 | CCTGGTATGATCAAA[C/G]GGCAGGTTATTTTTA | 137886 |
rs771680097 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448178 | TCAGCAATTCTTTTT[-/G]TTTTTTTTTTTTGAT | 137886 |
rs771689922 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446281 | GTCTCTATAAACTAT[C/T]CAAATACTAATGTGA | 137886 |
rs771709428 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429691 | TCCAAGGCAGATATC[A/G]TTTCCCCCCATTGTT | 137886 |
rs771737206 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421847 | AGAACATGATAGTTT[A/G]CTGACCTTGTGGAGG | 137886 |
rs771857253 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447633 | TCAGCATTAAAAACA[C/G]CCAAATTATTTTTAT | 137886 |
rs771953224 | snp | C/G | 0.000186689 | 0.00965969 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434817 | TTAATTAGTATGTAG[C/G]TGCCCACCCACTAAG | 137886 |
rs771966468 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414861 | CACATTCCATGGGGC[-/T]AGTGGCATTTTTGCT | 137886 |
rs772017956 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442734 | AGTGCCTAACAAAAT[A/C]ACAGAGTCATTTTTA | 137886 |
rs772095076 | snp | A/G | 0.000213242 | 0.0103236 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58411402 | TGGCGGAGGGCGGAG[A/G]CCCTGAGCCCGGCGA | 137886 |
rs772110974 | snp | A/G | 1.69258e-05 | 0.00290905 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434437 | AATGGTTTCAGTTTA[A/G]ATGATGGAGAATTGA | 137886 |
rs772127080 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419359 | TGGTCCACCTCCTTG[A/G]GCGGTATTTGAAATC | 137886 |
rs772152167 | snp | C/G | 1.67466e-05 | 0.00289362 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416853 | GTTATTATGTAGTTG[C/G]CCTTGGCAGAATTGT | 137886 |
rs772251703 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426859 | GGAGACTGTGCAGCC[A/G]CCCCCTAGGCTGGCT | 137886 |
rs772329825 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409617 | CCAGGCTGAAGTGCA[A/G]TGGTGCATCTCTGCT | 137886 |
rs772353004 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420758 | CCACTAAAACCAACT[C/G]TTCAATAGTTTTTGC | 137886 |
rs772383946 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422314 | AACTCAGGGTCTTAA[A/G]AGACTGAGAGACCTC | 137886 |
rs772508494 | in-del | -/AGA | 1.66015e-05 | 0.00288105 | cds-indel, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416906 | TCTTCCAAGTCTAAT[-/AGA]AGACCTAAAGCCACA | 137886 |
rs772601675 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440207 | ATATTATATGCCTCT[G/T]TCAGATTACCTGGTT | 137886 |
rs772706471 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431276 | ATCACAGTTCAAGAC[A/C]AGCCTGGCCAACATG | 137886 |
rs772732538 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414619 | TTTAAATTATCATTT[C/T]CTCTTTTGATGTAAT | 137886 |
rs772770976 | in-del | -/AAAAAAAAAAA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418243 | AGGACTCTGTCTCCA[-/AAAAAAAAAAA]AAAAAAAAAAAAATT | 137886 |
rs772775838 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448485 | AGCCTAAAGGTCAGC[A/T]GTTCTTAAGAAGATA | 137886 |
rs772777808 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448493 | GGTCAGCAGTTCTTA[A/G]GAAGATATGGTAAAC | 137886 |
rs772815537 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421971 | AGAGATGTTAATACC[A/G]GAGATATATTTGTAC | 137886 |
rs772927727 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437804 | AGTAGAGAAGGAGAA[A/G]GTGTTTTCAGGAGAA | 137886 |
rs772982136 | snp | A/G | 1.65693e-05 | 0.00287826 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433151 | TAACTCACTTGCTAT[A/G]TATTTTAGTCATTTA | 137886 |
rs772986171 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424827 | ATGCTGGACCGCCAT[A/G]TAGATAAATCGGTAC | 137886 |
rs773035241 | snp | C/T | 3.3605e-05 | 0.00409895 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433293 | ATTTGCTTCTAGTTA[C/T]TAAAACTGTTGGTTT | 137886 |
rs773110039 | in-del | -/TCTCTGTTGATGTCAG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424929 | CAGTCAACACCTTTC[-/TCTCTGTTGATGTCAG]TCTCTGTTGATGTCA | 137886 |
rs773142805 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58444936 | TGATGATTTAGATTG[A/G]ACTAAAGCCCAAATG | 137886 |
rs773161886 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436960 | AGAAAATTGGTACCA[A/T]GGAGTAGGGCATTGC | 137886 |
rs773207957 | snp | A/G | 1.65869e-05 | 0.00287979 | missense, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439745 | AGGTTCAAGGCTTTT[A/G]GTGGAGAAGGGCAAA | 137886 |
rs773244557 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427420 | GTGAGCCAAGATCAC[A/G]CCACTGCACTCTAGC | 137886 |
rs773331355 | snp | C/T | 0.000186477 | 0.00965421 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439585 | CTCAACAGTGTAGTT[C/T]AATTCTTGGAAAACT | 137886 |
rs773394739 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442742 | ACAAAATCACAGAGT[A/C]ATTTTTAATAGGGAG | 137886 |
rs773418603 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428029 | GAGAAGAAGGATAGG[C/T]TCAAAAGGATCAAAT | 137886 |
rs773422728 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58416373 | ATTTTCCTAAACACG[A/G]TGAAATTTATAAGTT | 137886 |
rs773477790 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427110 | AGGATGGAGAGAACA[A/G]GATAAAGAGAGAAAG | 137886 |
rs773546060 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429719 | GTTTTGTTCTATGTG[C/T]CAGTTCAGTGTGAAT | 137886 |
rs773552630 | snp | C/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409638 | CATCTCTGCTCACTG[C/T]AACCTCTGCTTCCCG | 137886 |
rs773617004 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419956 | TTGGTTTTGAACAAG[A/G]GGACTCGATTTTCAC | 137886 |
rs773664575 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420789 | CTTGTGTGAACTGCC[C/T]GTAGTGAAAAAAGAA | 137886 |
rs773811109 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414801 | CAGCCAGGTAGACTC[C/T]TTAATATCATTTTCC | 137886 |
rs773817082 | snp | A/T | 1.65798e-05 | 0.00287917 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447338 | CAGTTTTAAGTTTAC[A/T]TGAAAATATGATTTT | 137886 |
rs773872313 | snp | C/T | 1.6577e-05 | 0.00287893 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447420 | AACTTTATTGTACAG[C/T]CTCGTCCTGAATTTG | 137886 |
rs773919916 | in-del | -/TG | 1.66055e-05 | 0.0028814 | frameshift-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447527 | AGATATTCTTAACAC[-/TG]TGTTACTCCAGCAAC | 137886 |
rs773987509 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437319 | GGTGGAAGAAATTTC[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTGG | 137886 |
rs774041372 | snp | A/C | 2.0708e-05 | 0.0032177 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416994 | AAAAGAAATTATAAT[A/C]CTTTCTAAAAATTTA | 137886 |
rs774159628 | snp | C/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410194 | CCGAGGTGGGCAGAT[C/G]ATGAGGTCAGGAGAT | 137886 |
rs774165029 | snp | A/G | 4.04752e-05 | 0.00449844 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434361 | TGAATATATATATAT[A/G]TATATATATTTTTTT | 137886 |
rs774190191 | snp | A/G | | | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435325 | GTGGAGGTTAAATTC[A/G]TCTTTTAGAAGACTA | 137886 |
rs774192333 | snp | C/G | | | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451553 | TTTGAGTCCTGAATA[C/G]ATTGTTTTAACATGA | 137886 |
rs774339489 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441622 | TTGGAATTGAAGAAG[G/T]TAGCATAAAGGGAAG | 137886 |
rs774340751 | snp | C/G | 0.062435 | 0.165286 | utr-variant-5-prime, upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411354 | AAGTTGCGGCAGGTG[C/G]GTCCGCAGCGGGCGC | 137886 |
rs774406501 | snp | A/G | 4.99896e-05 | 0.00499923 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58445953 | TCTCCAGAAGAGGAG[A/G]ATAAATCAATACTTA | 137886 |
rs774507838 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441058 | AGTACAGTGGTGTAG[A/T]CATAGTTCACTGCAG | 137886 |
rs774571672 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420556 | ACTCTGGTACTTCAT[A/G]TACTGCAGGAAAATT | 137886 |
rs774573766 | snp | C/G | 1.66244e-05 | 0.00288304 | missense, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439757 | TTTAGTGGAGAAGGG[C/G]AAAAACTTGGAAGGT | 137886 |
rs774632686 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58439262 | AAAACACCCATATCA[A/G]TTTTCAGAACTTTCT | 137886 |
rs774669608 | in-del | -/A | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434170 | TTTGCAGCCATTGTC[-/A]GTTTGTTAAGCTGAA | 137886 |
rs774694541 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419777 | AACCAGAAAAAGAAC[C/G]AGCAGAACTTTAGTA | 137886 |
rs774752688 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429891 | GGTTATTAATCTTAC[A/G]TAAAGGTAATTTTTA | 137886 |
rs774831914 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431154 | CCTCTAGCCAATACC[A/G]GTCGGGTTTTCATCT | 137886 |
rs774857176 | snp | A/G | 0.000101963 | 0.0071394 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430637 | GTCCCTCTGAATGAA[A/G]CCACAAGAGCTTCAG | 137886 |
rs774912226 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436444 | ATGAGTCTTTATCAC[A/G]TAAGACAAATCTCCT | 137886 |
rs774956560 | snp | A/G | | | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58446007 | TCAGTGCCAACAACA[A/G]AAATTCAAATCAGGT | 137886 |
rs775018211 | snp | A/G | 5.00864e-05 | 0.00500407 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447556 | AACTAAAATAATATT[A/G]TTCCTGTCCATGCAG | 137886 |
rs775113749 | snp | A/G | 1.65861e-05 | 0.00287972 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433132 | AATAATCCTTTGTGA[A/G]TTTTAACTCACTTGC | 137886 |
rs775139543 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423048 | GTTTAGTAAGTAGAG[A/G]GCATACTCCAGCTCT | 137886 |
rs775165230 | snp | A/G/T | 0.000116034 | 0.00761609 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447437 | TCGTCCTGAATTTGC[A/G/T]GCTCTTGACTTTATT | 137886 |
rs775206480 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449277 | ACATTTTACATGGAA[C/T]ATTATTCTTGCCTAC | 137886 |
rs775240742 | snp | A/G | | | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435164 | CATAAAGTTGAGCAT[A/G]AACTGGGGAATTAAG | 137886 |
rs775307801 | in-del | -/AT | 0.072888 | 0.176441 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434348 | CTTATGTATATGTGA[-/AT]ATATATATATATATA | 137886 |
rs775343243 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417491 | TCTAATGTGTGACCT[A/C]CTAAATAGTATTTGT | 137886 |
rs775448101 | in-del | -/A | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58433612 | AGACCCTATCTCTTT[-/A]AAAAAAAAAAAAAAA | 137886 |
rs775481708 | snp | C/T | 5.01643e-05 | 0.00500796 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416856 | ATTATGTAGTTGGCC[C/T]TGGCAGAATTGTATG | 137886 |
rs775514770 | snp | A/C | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410992 | TGTGGTGACGATGTA[A/C]CATCCAATCCTTGAT | 137886 |
rs775528300 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424411 | GGTATTGTTGAGTTA[A/C]AATACAGTGATCTTT | 137886 |
rs775571725 | snp | A/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410520 | TCTTTTTTGAGACGG[A/T]TCCTCCCTGTGTCGC | 137886 |
rs775591641 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426772 | GCTGGCCCGAGGGAG[A/G]CCCGCTCGGGACCAG | 137886 |
rs775651576 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412640 | TCATCTTTCCTATTA[C/T]AAACCCACATCACTA | 137886 |
rs775791801 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58430433 | TTTTAAATAAAATAC[A/T]TTTATTTTCATAAGA | 137886 |
rs775817028 | snp | A/G | 1.69112e-05 | 0.0029078 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439787 | TAAAAATCCTAAAAT[A/G]AGAAAAATACCTTTG | 137886 |
rs775827088 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429737 | GTTCAGTGTGAATTT[A/G]GAATTGGATTGGAGA | 137886 |
rs775872066 | snp | A/G | 0.000116357 | 0.00762661 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58445962 | GAGGAGGATAAATCA[A/G]TACTTAATGCAGTTG | 137886 |
rs775913542 | in-del | AAAAAAATTTTTACCAAAA/TAGTAATTCTGTG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418271 | AAAAAAAAAAATTAA[lengthTooLong]ATGCCATTTAATATA | 137886 |
rs776007454 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443159 | CCTGCCCCTCACTCT[A/C]AGCAAATTTCTTTGC | 137886 |
rs776053089 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449954 | TAGGAGGCTCCTCAC[A/G]TATCTTTCCTGGAAA | 137886 |
rs776115510 | snp | A/G | 1.65869e-05 | 0.00287979 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58433242 | AAAATCAGCTGCAAG[A/G]TGTAGGTACAATAAT | 137886 |
rs776156090 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411799 | ACTTACTCCAGAAGA[A/G]AGGTTACTGTGGCCG | 137886 |
rs776276894 | snp | A/G | | | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435133 | AGTTATTTCTAAGTA[A/G]ATATGCAACTAAAGA | 137886 |
rs776281891 | snp | A/T | 3.31543e-05 | 0.00407137 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433144 | TGAATTTTAACTCAC[A/T]TGCTATGTATTTTAG | 137886 |
rs776282280 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58415538 | AAGAAAAAAAAATCT[C/T]GGGGAAAATGAAACA | 137886 |
rs776327741 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425687 | TAGTTCTCGAATTCT[G/T]CTATTTCAGCAACAT | 137886 |
rs776375001 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448992 | TCCTTGTCATTCCAC[C/T]TTCTACAGGACATCC | 137886 |
rs776388810 | snp | C/T | 1.67925e-05 | 0.00289758 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447575 | CTGTCCATGCAGTAG[C/T]ATGTGGGAATAGATG | 137886 |
rs776453437 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58439013 | TTGTTTAATAGCCTG[A/G]AACCTCCCATCTCCC | 137886 |
rs776496443 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437296 | AAGAGTGATGATCTA[C/G]GGTACCTGGTGGAAG | 137886 |
rs776649414 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424998 | AATTCCAGCACTGCC[A/G]TGCACCACGACTGGC | 137886 |
rs776754496 | snp | A/C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418565 | ATTAGAATTTTTGTC[A/C/G]GGTATGCTAGATAAG | 137886 |
rs776811594 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429419 | CTTGGGACAAGGGCT[C/T]CCATAGGCTCCTGCT | 137886 |
rs776834617 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411740 | TAGAATGACATTTTG[C/T]GGGGTCAGTTGGTCG | 137886 |
rs776851329 | snp | C/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410400 | CTTGGGCGACAGAGC[C/G]AGGCTCCGTCTCAAA | 137886 |
rs776891147 | snp | A/T | 1.6918e-05 | 0.00290839 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434438 | ATGGTTTCAGTTTAG[A/T]TGATGGAGAATTGAG | 137886 |
rs776901069 | snp | A/G | 1.66696e-05 | 0.00288696 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416869 | CCTTGGCAGAATTGT[A/G]TGAAGATGAAGTGAA | 137886 |
rs776912480 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442901 | ATTGTGCTTGCCACT[C/T]TCACTTACCTGAGAT | 137886 |
rs776957280 | in-del | -/ATTA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58439947 | CCATTATATCATAAT[-/ATTA]ATTAATTGTGATATT | 137886 |
rs777021906 | in-del | -/G | | | utr-variant-5-prime, upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411269 | CGGGGGCGCGGGTTC[-/G]GGTAGCGGGGACGCG | 137886 |
rs777184583 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428008 | CAACTATGAAACAGC[A/G]AAAGGGAGAAGAAGG | 137886 |
rs777208338 | snp | A/G | 4.97673e-05 | 0.00498811 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58445997 | TATTGATGATTCAGT[A/G]CCAACAACAAAAATT | 137886 |
rs777239855 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58415026 | TTCTATTATGTTCTT[C/T]ATATAATTCAACGTC | 137886 |
rs777241609 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427419 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCTAG | 137886 |
rs777265934 | snp | A/G | 2.08871e-05 | 0.00323158 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434535 | TGTATTCTATTTGTT[A/G]TGTAGAGTGGGACTT | 137886 |
rs777301808 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440362 | GCTTTGTGATTTTCA[A/G]TAGTTTTTAAACAGC | 137886 |
rs777309746 | snp | A/T | 1.86246e-05 | 0.00305155 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434403 | CCAAAAGGTTCAGAT[A/T]TTGCTTAAACTGTGG | 137886 |
rs777310950 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450813 | TTCAAAGAGGTGAAT[G/T]TACCTGTGCTAGGGT | 137886 |
rs777372989 | snp | A/G | 3.32469e-05 | 0.00407705 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416919 | AATAGACCTAAAGCC[A/G]CAGTCTTCAAGAGCC | 137886 |
rs777395330 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432604 | AGCCAGGGTGGTCTC[A/G]ATCTCCTGACCTCGT | 137886 |
rs777468500 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58416005 | AGGAGCATTTTAATC[-/T]TGTTTTGTTATGATT | 137886 |
rs777635715 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBXN2B | GRCh38.p7 | 8:58435105 | GTGTTATGATTAAAC[C/T]AGCTGAAAGTGGAGT | 137886 |
rs777681256 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412236 | GAACAGTTTTACTGT[A/G]TTACTTTACAACCAC | 137886 |
rs777705961 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58444305 | TAGTGCCAACTATAT[A/G]AAAGCACCATTTGAA | 137886 |
rs777717509 | snp | A/G | 1.66233e-05 | 0.00288295 | splice-acceptor-variant | UBXN2B | GRCh38.p7 | 8:58447388 | TGTCTTATTTCTTCA[A/G]GATCCTGGATGTCCG | 137886 |
rs777793945 | snp | C/T | 1.68766e-05 | 0.00290483 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416839 | TTTGTAACAAGCCTG[C/T]TATTATGTAGTTGGC | 137886 |
rs777878629 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428381 | AGAAAAACAAAAGTA[-/T]ACAAATTGGAAATAA | 137886 |
rs777916670 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422511 | AACATATAAGGCGAA[A/G]AGGGATGTCTTTGGA | 137886 |
rs777993862 | in-del | -/AGAGTTCAACTATGAAACAGCGAAAGGGAGA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427987 | ATGAAAGTCCAGGAG[lengthTooLong]AGAAGGATAGGCTCA | 137886 |
rs778056866 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422764 | CAAGATCAGTTTCCC[C/T]AAGTGCTGGTTCCAA | 137886 |
rs778101073 | in-del | -/TA | 1.84446e-05 | 0.00303677 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430472 | CTTTTTACTTCAGTT[-/TA]TGTCTGTTATCCTAA | 137886 |
rs778158646 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446757 | CTAACACATTTTATA[C/G]TCCGAAAAAAGTACA | 137886 |
rs778169713 | snp | A/G | 4.44069e-05 | 0.00471185 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430706 | AAATACATTGTTTCT[A/G]TATTTTACCTCCTCT | 137886 |
rs778252916 | snp | A/G | 0.000183629 | 0.00958022 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430591 | GAAAATTGTGAATGA[A/G]CTTTTCAAAGAGGCA | 137886 |
rs778282101 | snp | A/C | 1.65886e-05 | 0.00287993 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447509 | CCTGACACTGCTAGA[A/C]GCAGATATTCTTAAC | 137886 |
rs778319201 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450788 | ACCTTTCTCCAGGGT[C/T]ACTGTTTATTTCAAA | 137886 |
rs778378899 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440199 | TCACCACTATATTAT[A/G]TGCCTCTTTCAGATT | 137886 |
rs778431837 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438631 | GCCTATACCACCATT[C/G]TATCTTAGAAGTAAA | 137886 |
rs778443692 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449686 | ACCAGCGAGGCACCC[A/T]TCTTTAAGTTTCAAG | 137886 |
rs778516206 | in-del | -/TGA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429139 | CTTTCTCACTAAGAC[-/TGA]TGAGATAAAAAGGAA | 137886 |
rs778620503 | snp | G/T | 2.32221e-05 | 0.00340742 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434554 | AGAGTGGGACTTATT[G/T]TCTTAACAGACTACT | 137886 |
rs778657953 | snp | A/G | 1.65652e-05 | 0.0028779 | missense, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439690 | AGTGAATTTGGATAT[A/G]GAGGATCATCAGGAT | 137886 |
rs778854921 | snp | C/T | 1.66905e-05 | 0.00288876 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430557 | ACAGTGGATTAAATA[C/T]AGTTCGACCTTCAAC | 137886 |
rs778921334 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445136 | TTTAACCAAAAGAGC[A/G]CTCCTCTATTTTTGA | 137886 |
rs778940740 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422696 | TCTGGGAGTGCCCCA[A/G]TGGGGTGGTGCTGCT | 137886 |
rs778942804 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409884 | TTTATACATCAAAAC[A/G]ATCAGTATGCCAAAG | 137886 |
rs778950469 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58430443 | AATACTTTTATTTTC[A/G]TAAGACTATGTAGCT | 137886 |
rs779069501 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422220 | ACCCGTGTTCTGAAG[C/G]AATTCAAAGTTCAAT | 137886 |
rs779101701 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442561 | GAACTAAATCTTTTC[A/G]TGTGATATACAATTA | 137886 |
rs779143523 | in-del | -/T | 0.000153863 | 0.00876972 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416827 | TAGTGTTATACTTTG[-/T]TAACAAGCCTGTTAT | 137886 |
rs779197332 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448390 | TGTTGATCAGGCTGG[G/T]CTCGAACTCCGAACC | 137886 |
rs779236444 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414943 | TCAAATCTTGTTAAA[A/G]CAAAAAGTGTTTAAC | 137886 |
rs779335388 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449532 | ATAATTCCAACTGTG[C/G]ACTTGTGAACCTAGA | 137886 |
rs779350935 | snp | A/T | 1.65908e-05 | 0.00288012 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433122 | CTTTTTGCTGAATAA[A/T]CCTTTGTGAATTTTA | 137886 |
rs779579965 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417960 | TAATAGTAATTCAGG[C/T]GGGGAGTGGTGGCTT | 137886 |
rs779606134 | in-del | -/TGGAT | 1.76897e-05 | 0.00297398 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446113 | TGCTGTTATATACAC[-/TGGAT]TGCTTATCTAAGTAG | 137886 |
rs779662096 | in-del | -/TA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58430450 | TTATTTTCATAAGAC[-/TA]TGTAGCTTTTTACTT | 137886 |
rs779711238 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417171 | GCCAAAAGAAACTTA[C/T]GGAAAAATTACCTTA | 137886 |
rs779714037 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451221 | AACTGCCATTTTTGT[A/T]TATAATAGTCTTCCA | 137886 |
rs779986112 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428929 | GAAAAAATAGTTCTT[G/T]TCCTCTACCTTATAC | 137886 |
rs779990607 | snp | C/G | 1.6569e-05 | 0.00287824 | missense, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439721 | CAAGAATACATAAAA[C/G]CTAGATTGAGGTTCA | 137886 |
rs780039373 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427914 | GGAGGAAGAAAACTC[A/G]GTAAAATAGAGAAGG | 137886 |
rs780041221 | snp | A/G | 4.9755e-05 | 0.00498748 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447403 | GGATCCTGGATGTCC[A/G]GAACTTTATTGTACA | 137886 |
rs780148901 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432226 | TACAGCTTTACATTT[A/G]AAGCTATGATCTATT | 137886 |
rs780165059 | snp | A/G | 6.67668e-05 | 0.00577745 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416938 | TCTTCAAGAGCCCAC[A/G]GACACCACCTCAACG | 137886 |
rs780276370 | snp | G/T | 1.73598e-05 | 0.00294611 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446090 | TTCTTTACCAACAGT[G/T]TCCTGTTTGCTGTTA | 137886 |
rs780284235 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58439014 | TGTTTAATAGCCTGG[A/T]ACCTCCCATCTCCCT | 137886 |
rs780386073 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425389 | CAGCCTTGTGTGGCA[A/G]TGTAACTCTTCTTGG | 137886 |
rs780449299 | snp | A/C | 1.65682e-05 | 0.00287817 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58433213 | TTGTAAGCGGTCTGA[A/C]TATATCTATGGAGAA | 137886 |
rs780546765 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413719 | TTGCTTCCCAAAAGG[A/C]CTCCCAGCCCTGGGA | 137886 |
rs780587703 | in-del | -/TATT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446255 | AAATGAAATATGTGG[-/TATT]TATTTAAACAGTCTC | 137886 |
rs780629487 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424516 | ACATAAACTTTCTTG[C/T]GAAAGTTTGATCTTT | 137886 |
rs780667774 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412773 | TCCTGTGTCTTCATT[A/T]GTAAACTGAGGAAGG | 137886 |
rs780724846 | in-del | -/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419406 | CATTGTCATTTTAAG[-/C]CAAGACAGTTTCATT | 137886 |
rs780787573 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417368 | TCGTTTTTAAGGATA[C/T]GTGTGTTTCTTGAAG | 137886 |
rs780961169 | in-del | -/AGA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438791 | GTATTTTGTGATGTG[-/AGA]AGGACATGAGATTTG | 137886 |
rs781112570 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421840 | TTACATAAGAACATG[A/G]TAGTTTGCTGACCTT | 137886 |
rs781136593 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409822 | GCCTCGGCCTCCCAA[A/G]GAGTTGGGATTACAG | 137886 |
rs781193565 | snp | C/G | 1.71572e-05 | 0.00292888 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416823 | ATTCCTAGTGTTATA[C/G]TTTGTAACAAGCCTG | 137886 |
rs781294440 | snp | C/T | 3.31625e-05 | 0.00407188 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447494 | GCTAACAGATGAAAG[C/T]CTGACACTGCTAGAA | 137886 |
rs781298531 | in-del | -/TG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411633 | GTCGGGTCTTGACAC[-/TG]TGGTGGTCGTGAACA | 137886 |
rs781412798 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58444712 | AGGCCCTCAATTCCA[A/G]ATTAAAAAGAAATTC | 137886 |
rs781485608 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412553 | GGTGAACTTAATGTA[A/G]AATAGTTCCAGCTCC | 137886 |
rs781499846 | snp | A/C/T | 3.36963e-05 | 0.00410454 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416946 | AGCCCACGGACACCA[A/C/T]CTCAACGGTAAGTTT | 137886 |
rs781682316 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424065 | TTAATTCTCATTTGG[C/T]CAAAAATAGAAGCCA | 137886 |
rs781689733 | snp | A/G | 3.87928e-05 | 0.00440396 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434514 | GAGAGGGTAAGATGT[A/G]TTATTTGTATTCTAT | 137886 |
rs781720045 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437378 | TGTCACCCAGGCTGG[A/C]GTGCAGTGGCGCGAT | 137886 |
rs781749595 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422960 | TGTGACCGTCTGTTA[C/G]ACTAGTGGCCTCCCA | 137886 |
rs781752060 | in-del | -/TAT | 2.23092e-05 | 0.00333978 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445865 | CTTCAGTTTGTCATA[-/TAT]TTTACACATTCAGAT | 137886 |
rs781776995 | in-del | -/T/TT | 0.18006 | 0.249293 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434367 | ATATATATATATATA[-/T/TT]TATTTTTTTTTTTTC | 137886 |
rs796077655 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441373 | TATATATATATGTAT[A/G]TGTATATATATGTAT | 137886 |
rs796116042 | in-del | -/AT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441351 | TGTTGTGATCAACAT[-/AT]ATATATATATATATA | 137886 |
rs796144343 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418266 | AAAAAAAAAAAAAAA[A/G]TTAATAGTAATTCTG | 137886 |
rs796539383 | in-del | -/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437960 | AGGCAGCCCCCCCCC[-/C]AACCCCCATCACAGG | 137886 |
rs796616041 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428950 | TACCTTATACCACCT[A/G]TAAACGTCAGTTCCA | 137886 |
rs796633378 | in-del | -/TT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434370 | ATATATATATATATA[-/TT]TTTTTTTTTTCTATA | 137886 |
rs796815547 | in-del | -/CT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442899 | AGATTGTGCTTGCCA[-/CT]CTCACTTACCTGAGA | 137886 |