SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs537602 | snp | C/T | 0.0520825 | 0.152737 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62681104 | TTCTTAGAAGGCAAA[C/T]CCTGAATCCTGAAAA | 51035 |
rs644616 | snp | G/T | 0.3744 | 0.216852 | intron-variant, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62677326 | TGAGTAAGAGAGAGG[G/T]ATGGGTTTAAATACA | 51035 |
rs1050329 | snp | C/T | 0 | 0 | missense, utr-variant-3-prime | UBXN1 | GRCh38.p7 | 11:62677570 | GTCCTGTTCCCTCTT[C/T]TCCCAGCCAGGAGCC | 51035 |
rs1050383 | snp | A/C | 0 | 0 | missense | UBXN1 | GRCh38.p7 | 11:62676920 | TCTATGTGGAGCTCC[A/C]CCGTGGGGAGGAACT | 51035 |
rs1131097 | snp | C/T | | | synonymous-codon, utr-variant-3-prime | UBXN1 | GRCh38.p7 | 11:62677527 | GGAGTATGACCAGTG[C/T]CGCATACAGGTCAGG | 51035 |
rs1804042 | snp | A/G | | | missense | UBXN1 | GRCh38.p7 | 11:62676893 | AACTAGGTGGGGGCC[A/G]GGACCCTGTGCAATT | 51035 |
rs2276297 | snp | C/G/T | 0.000115312 | 0.00759235 | intron-variant | UBXN1 | GRCh38.p7 | 11:62678437 | ATCGGTATTATTATC[C/G/T]CTTCAGATTCTCCTC | 51035 |
rs2730036 | snp | G/T | 0.00873346 | 0.0655016 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680962 | CCTCAAGTGGTGGGT[G/T]ATGAATCTGCACAAT | 51035 |
rs2957120 | snp | C/T | | | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62679752 | agagcgagactccct[C/T]ttaaaaaaaaaaaaa | 51035 |
rs11231184 | snp | A/C | 0.263535 | 0.249633 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680091 | GGCTGTTCTCGAACT[A/C]CTGACCTTAGGTGAT | 51035 |
rs11543359 | snp | C/T | 0.00173929 | 0.0294384 | missense, intron-variant | UBXN1 | GRCh38.p7 | 11:62678549 | CCTTTAGAGACTCCC[C/T]TTGGACATATCCTGG | 51035 |
rs34676382 | in-del | -/G | 0.0517044 | 0.152246 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62679397 | GAGCAGAAGAAATGT[-/G]CTTGCTCTTTGGCCC | 51035 |
rs60001928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62677384 | TCCCAAGAGTAGAGA[G/T]AGGATTTCAAAAGTC | 51035 |
rs60379113 | snp | C/T | | | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62679547 | ATCTAGGACAACTTA[C/T]TTTTTTTTTTATTTT | 51035 |
rs61319947 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680929 | CTGGCAAGGCAGAGT[A/T]TGTAAATGCTGGTAG | 51035 |
rs67084516 | in-del | -/G | | | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62679398 | AGCAGAAGAAATGTC[-/G]TTGCTCTTTGGCCCA | 51035 |
rs71056543 | in-del | -/T | | | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680357 | TCTCTCTCTCTCTCC[-/T]TTTTTTTTTTTTTTT | 51035 |
rs71496933 | snp | A/G | 0.5 | 0 | downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62676173 | TGAACCTGGGAGGCA[A/G]AGGTTGCAGTGAGCT | 51035 |
rs75157237 | snp | C/T | 0 | 0 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62679727 | CACCATGCCCAGCTT[C/T]TTTTTTTTTTTTTTT | 51035 |
rs76786865 | snp | C/T | 0.0193772 | 0.0965046 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62679453 | CATCCTCTGCCTGAC[C/T]GCCAAAGGGATTTTT | 51035 |
rs78756652 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62679468 | TGCCAAAGGGATTTT[G/T]GCAAAACACAATCAT | 51035 |
rs80252183 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62679469 | GCCAAAGGGATTTTT[G/T]CAAAACACAATCATG | 51035 |
rs111264343 | snp | C/G | 0 | 0 | splice-acceptor-variant | UBXN1 | GRCh38.p7 | 11:62678744 | GCCAGAGCCTTCTCC[C/G]TGGGGGCAGAAACAC | 51035 |
rs111325595 | snp | C/G | 0.0121623 | 0.0770273 | missense | UBXN1 | GRCh38.p7 | 11:62676912 | CCCCACCTAGTTCCT[C/G]CCCACGGTGGAGCTC | 51035 |
rs111403744 | snp | A/C/T | 0 | 0 | splice-acceptor-variant | UBXN1 | GRCh38.p7 | 11:62678745 | CCAGAGCCTTCTCCC[A/C/T]GGGGGCAGAAACACC | 51035 |
rs112061935 | snp | A/C/G | 0 | 0 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62676642 | GAAGGCACGAGTCCT[A/C/G]AAGATGGAAGAAAAC | 51035 |
rs112293944 | snp | A/C/T | 0 | 0 | splice-acceptor-variant, utr-variant-3-prime, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62676641 | AGAAGGCACGAGTCC[A/C/T]GAAGATGGAAGAAAA | 51035 |
rs112860804 | snp | C/T | 0.5 | 0 | intron-variant | UBXN1 | GRCh38.p7 | 11:62678315 | AAGACGACCCTCAGA[C/T]ACGTGAGATTGTTGT | 51035 |
rs113297200 | snp | C/T | 0.0267878 | 0.112589 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680274 | AAGCGATCCTCCCAC[C/T]TCAGCCTCCCAAGTA | 51035 |
rs115234949 | snp | A/G/T | 0.00103815 | 0.0227599 | intron-variant | UBXN1 | GRCh38.p7 | 11:62678265 | ATGTGGAAAGGTCAA[A/G/T]GTTCTTTGACCAGAC | 51035 |
rs117555780 | snp | A/G | 0.00240238 | 0.0345748 | missense | UBXN1 | GRCh38.p7 | 11:62678051 | TGCGCTGCCGTTCCC[A/G]TTCCAATGCCTCCCG | 51035 |
rs140112798 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | UBXN1 | GRCh38.p7 | 11:62678342 | TTGTTACTGTACCTC[C/T]TAGTTTGTTCCTGTC | 51035 |
rs140703742 | snp | A/C | | | intron-variant, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62677291 | CAAATAAAAACATGA[A/C]CAAGTAAAAGGGTAA | 51035 |
rs142043303 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62681042 | CACCAACCAGTCTCC[A/G]CCTAGGATGTCCTGT | 51035 |
rs142782985 | snp | A/C/G | 0.00422414 | 0.0457633 | missense, synonymous-codon | UBXN1 | GRCh38.p7 | 11:62678707 | GTCCATCGCAGCCTC[A/C/G]ATGCCCTGGTTCCCT | 51035 |
rs142987858 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-3-prime | UBXN1 | GRCh38.p7 | 11:62677597 | GGACCTGGCTCTGGT[A/G]CCACTGGGGGTGGCT | 51035 |
rs143908470 | snp | C/T | 0.000131774 | 0.00811601 | synonymous-codon, intron-variant | UBXN1 | GRCh38.p7 | 11:62678362 | TTGTTCCTGTCTTTC[C/T]TCTTCACTCAAAGCG | 51035 |
rs145809989 | snp | C/G | 0.000502159 | 0.0158375 | synonymous-codon | UBXN1 | GRCh38.p7 | 11:62676958 | AGCTGCCAGCTGTTC[C/G]CGGGCCCGGAACGTC | 51035 |
rs145824608 | snp | C/T | 0.0156829 | 0.0871522 | intron-variant, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62677472 | CTGGGCACCTTAACA[C/T]GGAACAAAGGGGTCC | 51035 |
rs145840266 | snp | A/G | 0.00011596 | 0.00761359 | synonymous-codon, intron-variant | UBXN1 | GRCh38.p7 | 11:62678538 | GGGCTCCCGTCCCAG[A/G]ATATGTCCAAGGGGA | 51035 |
rs146130025 | snp | A/C/G | 0.000153988 | 0.00877328 | missense | UBXN1 | GRCh38.p7 | 11:62677958 | CGGCCTTTTCCCTCC[A/C/G]CCTCTCCTCAGCAGC | 51035 |
rs147015299 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680451 | GCTCACTGCAACCTC[A/T]GCCTGCCCCGGGTTT | 51035 |
rs148067164 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680758 | TCGCCCTCCCAAAGT[A/G]CTAAGATTAAAGGCG | 51035 |
rs149072490 | snp | A/C/T | 0.0142736 | 0.0832652 | intron-variant, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62677365 | AGGTGAAATTTGATA[A/C/T]CTTTCCCAAGAGTAG | 51035 |
rs150254212 | snp | C/G | 0.00211987 | 0.0324875 | utr-variant-3-prime, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62676512 | ATGTACAGAACTCAG[C/G]GTCTATTTATTAGGA | 51035 |
rs150573265 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680834 | CTGACTTCCTTCTGC[A/G]CCCACCTTGGCTTTT | 51035 |
rs180797778 | snp | G/T | | | intron-variant, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62677460 | AAAAGCTCTGAGCTG[G/T]GCACCTTAACACGGA | 51035 |
rs181167564 | snp | A/G | 1.64798e-05 | 0.00287047 | intron-variant, utr-variant-3-prime | UBXN1 | GRCh38.p7 | 11:62676677 | TTGAACCACAAGGAT[A/G]CTTGGTTTTTGCTCC | 51035 |
rs181209150 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680273 | CAAGCGATCCTCCCA[C/G]TTCAGCCTCCCAAGT | 51035 |
rs181580021 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | UBXN1 | GRCh38.p7 | 11:62678971 | GTGTGTGACGAGAAG[A/G]AGGGCGGGAAGGGTC | 51035 |
rs181937946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62677202 | AGCTCCCTCACAACC[C/T]AAGAAAGACAAGGAT | 51035 |
rs182268006 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62679619 | AGTGCAATAGTGCAG[C/T]GGCGCGATCTCTGCT | 51035 |
rs182406651 | snp | A/G | | | intron-variant | UBXN1 | GRCh38.p7 | 11:62677879 | ACATCAACAAAGCAA[A/G]TCTTGATTTCTTTCT | 51035 |
rs183444513 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant | UBXN1 | GRCh38.p7 | 11:62678436 | AATCGGTATTATTAT[C/T]CCTTCAGATTCTCCT | 51035 |
rs183990773 | snp | C/T | 0.00406236 | 0.0448852 | intron-variant | UBXN1 | GRCh38.p7 | 11:62678825 | GAGACAGGTCCGCGA[C/T]CCCCCACACCCGCAG | 51035 |
rs184547788 | snp | C/G | 0.0193772 | 0.0965046 | downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62676014 | GGGAGGCCAAGGCAG[C/G]CGAATCACAAGGTCA | 51035 |
rs185023184 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62676197 | GTGAGCTGAGATTGC[A/G]CCACTGCACTCTAGC | 51035 |
rs185455489 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680470 | TGCCCCGGGTTTAAG[C/T]GATTCTCCTGCCCGA | 51035 |
rs185811645 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant | UBXN1 | GRCh38.p7 | 11:62679020 | CTCGACACCCGCCGA[C/T]GGGCGCTCGCTCTCT | 51035 |
rs186011118 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680157 | AGGCGTGAGCCACCA[C/T]ACCCAGCTATTTTTG | 51035 |
rs186663136 | snp | C/T | 0.00184672 | 0.0303307 | missense, utr-variant-3-prime | UBXN1 | GRCh38.p7 | 11:62677580 | TGGGAGAAGAGGGAA[C/T]AGGACCTGGCTCTGG | 51035 |
rs187182066 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62677227 | AAGGATAAGATTATA[C/T]AAAAGAATCTGGATA | 51035 |
rs187402335 | snp | A/T | 0.00709018 | 0.059117 | intron-variant | UBXN1 | GRCh38.p7 | 11:62678142 | CCGAGGGAAAACAGT[A/T]CAAGAGAAATGGACA | 51035 |
rs188919973 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62677111 | TTCTTAGATTGAACC[A/G]GCACAACTACTATTT | 51035 |
rs189268255 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | UBXN1 | GRCh38.p7 | 11:62678955 | CTTCCGCGGGGACCT[A/G]GTGTGTGACGAGAAG | 51035 |
rs189468261 | snp | C/G | 0.0142736 | 0.0832652 | downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62676020 | CCAAGGCAGGCGAAT[C/G]ACAAGGTCAGGAGTT | 51035 |
rs189483797 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62676302 | ACCATAGGAGTAAAA[C/G]GTGCCATCCAATGTA | 51035 |
rs189551187 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680232 | TGGTGCAATCTTGAC[A/G]TACTGCAACCTCAGC | 51035 |
rs190183819 | snp | A/G | 1.65636e-05 | 0.00287776 | intron-variant | UBXN1 | GRCh38.p7 | 11:62677637 | CACTGCCACCATACT[A/G]AAGGGCAAAGTAAAA | 51035 |
rs190289265 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62679612 | AGACTGGAGTGCAAT[A/C]GTGCAGTGGCGCGAT | 51035 |
rs190314508 | snp | A/C | 0.00709112 | 0.0591208 | intron-variant | UBXN1 | GRCh38.p7 | 11:62678143 | CGAGGGAAAACAGTT[A/C]AAGAGAAATGGACAG | 51035 |
rs190659124 | snp | A/T | | | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680784 | AGGCGTGAGCTACAT[A/T]CTCGGCCATCTGGGA | 51035 |
rs191200342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62677424 | GAAGGGAGAGATTTG[A/G]CAAAGGGCACGTTAA | 51035 |
rs191821120 | snp | C/T | 0.00109055 | 0.0233257 | intron-variant | UBXN1 | GRCh38.p7 | 11:62678773 | ACCATGAATAGCGCC[C/T]ACGAGCCATGGTGAC | 51035 |
rs192301227 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62676031 | GAATCACAAGGTCAG[A/G]AGTTTGAGACCAGCC | 51035 |
rs192560705 | snp | C/G | 0.00398564 | 0.0444627 | downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62676010 | CTTTGGGAGGCCAAG[C/G]CAGGCGAATCACAAG | 51035 |
rs192772658 | snp | A/G | | | intron-variant | UBXN1 | GRCh38.p7 | 11:62678476 | CTGAATAATCACACC[A/G]TGGACCCTCAGTCAG | 51035 |
rs199643316 | snp | A/C | | | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680646 | ACAGGTGTGAGCCAC[A/C]GCGCCCGGCCTAATT | 51035 |
rs199667995 | snp | A/G | 3.30836e-05 | 0.00406702 | missense, intron-variant | UBXN1 | GRCh38.p7 | 11:62678518 | CCGCCTTGCTCTGAG[A/G]AAGTGGGCTCCCGTC | 51035 |
rs199740068 | snp | A/C | 0.00037946 | 0.013769 | missense | UBXN1 | GRCh38.p7 | 11:62676877 | GGGGAAGCCACTGAG[A/C]AATTGCACAGGGTCC | 51035 |
rs199926045 | snp | C/T | 6.62383e-05 | 0.00575454 | intron-variant | UBXN1 | GRCh38.p7 | 11:62677677 | AGGTACTCACCCATC[C/T]TCAGGTGAAACAGAT | 51035 |
rs200124299 | snp | A/G | 0.00288079 | 0.0378431 | intron-variant | UBXN1 | GRCh38.p7 | 11:62678623 | GGGAAAGTGGGCGGG[A/G]AGGTTAGCTTTGAGG | 51035 |
rs200272023 | snp | A/G | 0.0002481 | 0.011135 | synonymous-codon, intron-variant | UBXN1 | GRCh38.p7 | 11:62678517 | GCCGCCTTGCTCTGA[A/G]GAAGTGGGCTCCCGT | 51035 |
rs200441645 | snp | A/G | 0.000955062 | 0.0218316 | intron-variant | UBXN1 | GRCh38.p7 | 11:62677859 | ACAAGAAGAAATTAG[A/G]TCAGACATCAACAAA | 51035 |
rs200445984 | snp | A/C | | | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680602 | GACCTCATGATCCAC[A/C]CACCTTGGCCTCCCA | 51035 |
rs200497942 | snp | A/G/T | 0.000164826 | 0.00907667 | synonymous-codon | UBXN1 | GRCh38.p7 | 11:62678100 | CTCCCGCTGCTTCTG[A/G/T]GCCACCAGCTCCAAC | 51035 |
rs200509247 | snp | A/C | 1.6476e-05 | 0.00287014 | intron-variant | UBXN1 | GRCh38.p7 | 11:62678452 | CCTTCAGATTCTCCT[A/C]GGACCCTCCTGAATA | 51035 |
rs200746021 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680649 | GGTGTGAGCCACCGC[C/G]CCCGGCCTAATTTTT | 51035 |
rs200999814 | snp | C/T | 0.00199792 | 0.0315431 | missense | UBXN1 | GRCh38.p7 | 11:62677934 | GCCCAGACCTGGCTG[C/T]TAACTCCTCGGCCTT | 51035 |
rs201079442 | snp | C/T | 1.64735e-05 | 0.00286993 | intron-variant, utr-variant-3-prime | UBXN1 | GRCh38.p7 | 11:62677762 | CTCCATTACCCGTGG[C/T]GTCTTCTCAGTCACC | 51035 |
rs201136792 | snp | C/G | 4.48119e-05 | 0.00473328 | intron-variant | UBXN1 | GRCh38.p7 | 11:62678821 | GGCCGAGACAGGTCC[C/G]CGACCCCCCACACCC | 51035 |
rs201175971 | snp | A/G | 4.98434e-05 | 0.00499192 | synonymous-codon, intron-variant | UBXN1 | GRCh38.p7 | 11:62678574 | TAAAGGCTCGTCCAC[A/G]TCGGGGTCGTCTTCG | 51035 |
rs201237878 | in-del | -/T | | | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680355 | TTCTCTCTCTCTCTC[-/T]CTTTTTTTTTTTTTT | 51035 |
rs201490859 | snp | A/G | 0.000329408 | 0.0128295 | missense, intron-variant | UBXN1 | GRCh38.p7 | 11:62678399 | CCTTCTCCGGCAGCA[A/G]AACCAGATCCTACAA | 51035 |
rs201587730 | snp | A/G | 0.00299544 | 0.0385843 | utr-variant-3-prime, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62676575 | GGTCACAGAGGGACA[A/G]TGGGACAAAGGCCCT | 51035 |
rs201663354 | snp | A/C | | | upstream-variant-2KB | UBXN1 | GRCh38.p7 | 11:62680604 | CCTCATGATCCACCC[A/C]CCTTGGCCTCCCAGA | 51035 |
rs201705756 | snp | C/G | 0.000968228 | 0.0219813 | intron-variant | UBXN1 | GRCh38.p7 | 11:62678679 | CTCCGCCACCCGGGA[C/G]GAGCGCTTACCAGTC | 51035 |
rs201898144 | snp | A/G | 0.000164853 | 0.00907741 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBXN1 | GRCh38.p7 | 11:62676672 | CAGGCTTGAACCACA[A/G]GGATACTTGGTTTTT | 51035 |
rs202070522 | snp | A/G | 3.31318e-05 | 0.00406999 | missense, intron-variant | UBXN1 | GRCh38.p7 | 11:62678539 | GGCTCCCGTCCCAGG[A/G]TATGTCCAAGGGGAG | 51035 |
rs202185109 | snp | C/G | 0.000181197 | 0.00951659 | intron-variant | UBXN1 | GRCh38.p7 | 11:62677851 | AAATGTAGACAAGAA[C/G]AAATTAGGTCAGACA | 51035 |