SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2233 | snp | C/G | 0.471863 | 0.115225 | intron-variant | UBASH3B | GRCh38.p7 | 11:122713899 | TGGATATAAACATCT[C/G]ATGGAAGGCTGCACT | 84959 |
rs2234 | snp | G/T | 0.181659 | 0.240478 | intron-variant | UBASH3B | GRCh38.p7 | 11:122713967 | CCCCTGATAGTTCTG[G/T]GAGCCACCTAAACTC | 84959 |
rs2361 | snp | A/G | 0.181659 | 0.240478 | intron-variant | UBASH3B | GRCh38.p7 | 11:122714181 | CGAAGGGGGAGCCCC[A/G]CTAAAGAAACTGATG | 84959 |
rs2362 | snp | A/G | 0.181978 | 0.240568 | intron-variant | UBASH3B | GRCh38.p7 | 11:122714172 | AGCCCCACTAAAGAA[A/G]CTGATGGGGCAGATG | 84959 |
rs866904 | in-del | -/C | 0.181659 | 0.240478 | intron-variant | UBASH3B | GRCh38.p7 | 11:122713974 | ATCCATGCCCCTGAT[-/C]AGTTCTGTGAGCCAC | 84959 |
rs871843 | snp | A/G | 0.482234 | 0.0925596 | intron-variant | UBASH3B | GRCh38.p7 | 11:122741587 | CCCACCAGGAGACCC[A/G]CGAGGATTTCAGGCT | 84959 |
rs871844 | snp | C/T | 0.467845 | 0.122652 | intron-variant | UBASH3B | GRCh38.p7 | 11:122741504 | ACTATGTGAACTGAC[C/T]TAGATCTTAAAGAGA | 84959 |
rs871845 | snp | C/T | 0.499502 | 0.0157669 | intron-variant | UBASH3B | GRCh38.p7 | 11:122741652 | CTTACAGGTCTGTGC[C/T]CTCCCAAGCAAAGCA | 84959 |
rs872412 | snp | C/T | 0.289942 | 0.246789 | intron-variant | UBASH3B | GRCh38.p7 | 11:122794448 | ctgacctcaggtgat[C/T]cgcctgcctcggcgt | 84959 |
rs872413 | snp | A/T | 0.2822 | 0.247918 | intron-variant | UBASH3B | GRCh38.p7 | 11:122794674 | TGCTGGCCAGAGCAG[A/T]TAACACCTTCCTTAT | 84959 |
rs872414 | snp | A/G | 0.495715 | 0.0460893 | synonymous-codon | UBASH3B | GRCh38.p7 | 11:122794729 | CTTAAATACATCGTC[A/G]TCCAACTCTCTCACG | 84959 |
rs873590 | snp | G/T | 0.461813 | 0.132798 | intron-variant | UBASH3B | GRCh38.p7 | 11:122799682 | TGTTTGCCTCCTGTT[G/T]ACAGCAGCAAGGGTG | 84959 |
rs884392 | snp | C/T | 0.279991 | 0.248195 | intron-variant | UBASH3B | GRCh38.p7 | 11:122745845 | CCTATCGGGAGATGA[C/T]CTCTGCCCCAGAAGG | 84959 |
rs884393 | snp | A/G | 0.300926 | 0.244758 | intron-variant | UBASH3B | GRCh38.p7 | 11:122745618 | CTGTGGGTCAATAAT[A/G]TCTTTGTAAAGGAAG | 84959 |
rs885325 | snp | C/T | 0.368529 | 0.220116 | intron-variant | UBASH3B | GRCh38.p7 | 11:122676043 | CTAAAGCCAGATAAA[C/T]TTCAGTGCATTGGCA | 84959 |
rs938630 | snp | C/T | 0.494315 | 0.0530107 | intron-variant | UBASH3B | GRCh38.p7 | 11:122716308 | CTACATGCCTGTAGT[C/T]CCAGCAAGCTGGGAG | 84959 |
rs938631 | snp | C/T | 0.373196 | 0.217538 | intron-variant | UBASH3B | GRCh38.p7 | 11:122712462 | CTGGGTCCATTTGGG[C/T]TGCTGAGAAAGCCCC | 84959 |
rs938632 | snp | A/G | 0.370162 | 0.219229 | intron-variant | UBASH3B | GRCh38.p7 | 11:122712435 | CCCCTCTCGTGTGAC[A/G]TGCGTCCCCCACCAA | 84959 |
rs949300 | snp | A/T | 0.48666 | 0.0805725 | intron-variant | UBASH3B | GRCh38.p7 | 11:122682431 | TCCTTGCCCCACAAC[A/T]GGGACAAGTGAACTT | 84959 |
rs955049 | snp | C/T | 0.24932 | 0.249999 | intron-variant | UBASH3B | GRCh38.p7 | 11:122704246 | CTGAATCACAGTCTC[C/T]TGAGTCTTCCTCTGA | 84959 |
rs955051 | snp | G/T | 0.235471 | 0.249577 | synonymous-codon | UBASH3B | GRCh38.p7 | 11:122789210 | CAGCACCAGCGAGGG[G/T]TGGATCTATGGCACG | 84959 |
rs1000722 | snp | C/T | 0.466721 | 0.124627 | intron-variant | UBASH3B | GRCh38.p7 | 11:122717441 | TGTGACAAGGACATC[C/T]TCCTCCCTACCCCTT | 84959 |
rs1000723 | snp | G/T | | | intron-variant | UBASH3B | GRCh38.p7 | 11:122715993 | TGCTTCCTTTCTTTG[G/T]CCCTGTTTCAGCTTT | 84959 |
rs1008862 | snp | A/G | 0.444931 | 0.15653 | intron-variant | UBASH3B | GRCh38.p7 | 11:122686190 | ACTTAAGCAGTCCCA[A/G]ATAATCATGTTCCCC | 84959 |
rs1060706 | snp | C/T | | | utr-variant-3-prime | UBASH3B | GRCh38.p7 | 11:122810344 | TTAGGTAGAGCCAAG[C/T]TGAGGAATCCTTTTA | 84959 |
rs1105365 | snp | C/T | 0.167158 | 0.235875 | intron-variant | UBASH3B | GRCh38.p7 | 11:122795487 | CCTGTTTCTGCATTC[C/T]GTCTTTCTGATGCAG | 84959 |
rs1106243 | snp | A/G | 0.489142 | 0.0728777 | intron-variant | UBASH3B | GRCh38.p7 | 11:122740722 | GCCATCTGTGTACAT[A/G]TGTGTGGGGCAAGGG | 84959 |
rs1122475 | snp | C/T | 0.437965 | 0.164831 | intron-variant | UBASH3B | GRCh38.p7 | 11:122752685 | TTATTTTCTTGGAGG[C/T]ATGCATGATGGAATG | 84959 |
rs1124106 | snp | A/C | 0.161596 | 0.233848 | intron-variant | UBASH3B | GRCh38.p7 | 11:122661878 | AAAAAAAAAAACAAA[A/C]AAAAAAATACCTTGA | 84959 |
rs1316522 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | UBASH3B | GRCh38.p7 | 11:122696905 | GGGTGGGGGTTCCTC[C/T]CGCCCTGCCCTGTGC | 84959 |
rs1344168 | snp | A/G | 0.250849 | 0.250298 | intron-variant | UBASH3B | GRCh38.p7 | 11:122704229 | GGTGTCATATGGAGC[A/G]TCTGAATCACAGTCT | 84959 |
rs1344169 | snp | A/G | 0.330947 | 0.236533 | intron-variant | UBASH3B | GRCh38.p7 | 11:122704059 | ACTCAGGGTGCCTGC[A/G]GCGGTGGGGCTTTTG | 84959 |
rs1540108 | snp | C/T | 0.301273 | 0.244686 | utr-variant-3-prime | UBASH3B | GRCh38.p7 | 11:122809891 | TTCAAGAATAAACCA[C/T]ACCAGTGAACAAGAA | 84959 |
rs1540109 | snp | C/T | 0.335161 | 0.261551 | utr-variant-3-prime | UBASH3B | GRCh38.p7 | 11:122810546 | CAGCCCTATCCCCCC[C/T]CCTTGCTTCTGTGAA | 84959 |
rs1540110 | snp | A/C | 0 | 0 | intron-variant | UBASH3B | GRCh38.p7 | 11:122749031 | GACCTCTCCAGGTCC[A/C]GGAGAACATAAAGCT | 84959 |
rs1540111 | snp | A/T | 0.206029 | 0.246103 | intron-variant | UBASH3B | GRCh38.p7 | 11:122748693 | CCCTTGGATGGACAC[A/T]CACAGAGCTCTTGTG | 84959 |
rs1540112 | snp | A/G | 0.177503 | 0.239258 | intron-variant | UBASH3B | GRCh38.p7 | 11:122748584 | CAAGAAATGCTTTGT[A/G]GTAATAAATTGCATA | 84959 |
rs1540113 | snp | C/T | 0.167484 | 0.23599 | intron-variant | UBASH3B | GRCh38.p7 | 11:122748183 | TGGAATGATGGATTT[C/T]GTCAGTTTTAAACCA | 84959 |
rs1557455 | snp | A/G | 0.203882 | 0.245709 | utr-variant-3-prime | UBASH3B | GRCh38.p7 | 11:122810826 | AGATATATTATTTGC[A/G]GCAAGAAGTTCATTC | 84959 |
rs1557456 | snp | C/T | 0.359152 | 0.224913 | intron-variant | UBASH3B | GRCh38.p7 | 11:122717777 | AAGTCACAGGGGGCC[C/T]GGTCAACCACCAGCA | 84959 |
rs1557457 | snp | A/G | 0.34437 | 0.231505 | intron-variant | UBASH3B | GRCh38.p7 | 11:122717925 | CTTTTTTTTTTTTTC[A/G]GACAAGTCTCACTCT | 84959 |
rs1557458 | snp | A/T | | | intron-variant | UBASH3B | GRCh38.p7 | 11:122656765 | CGGGAGCGTGGGTGT[A/T]CCTGCGTGTGCATTG | 84959 |
rs1557459 | snp | G/T | | | intron-variant | UBASH3B | GRCh38.p7 | 11:122656775 | GGTGTACCTGCGTGT[G/T]CATTGATGGGGAGGA | 84959 |
rs1557460 | snp | C/G | 0 | 0 | intron-variant | UBASH3B | GRCh38.p7 | 11:122656849 | TCGTCAGTGGTGACG[C/G]CAGCTCAGAAATCTG | 84959 |
rs1879885 | snp | C/G | 0.179105 | 0.239737 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | UBASH3B | GRCh38.p7 | 11:122773846 | ATGAAATATATCCGA[C/G]TGAAATTTAATTTAT | 84959 |
rs1893998 | snp | A/T | 0.367913 | 0.220446 | | | GRCh38.p7 | 11:122674909 | AAACCCTGTCTCTAC[A/T]AAAAATACGAAAATT | 84959 |
rs1894078 | snp | A/G | 0.3742 | 0.216966 | | | GRCh38.p7 | 11:122728243 | GGGGAATATTTAGCC[A/G]TCCACGTCATTTCTG | 84959 |
rs1894079 | snp | C/T | 0.3744 | 0.216852 | | | GRCh38.p7 | 11:122728340 | GTTGGCACAGACATC[C/T]TTCTGCCTTTTCTTT | 84959 |
rs1894080 | snp | C/T | 0.3746 | 0.216737 | | | GRCh38.p7 | 11:122728798 | ACATCTGTGTACTTC[C/T]AACATCTAGCACAGG | 84959 |
rs1894081 | snp | A/G | 0.424814 | 0.178718 | | | GRCh38.p7 | 11:122745351 | ATACTTGCTGAATGA[A/G]TGCACTGACCCCTGC | 84959 |
rs1894082 | snp | C/T | 0.486067 | 0.0822953 | | | GRCh38.p7 | 11:122745197 | GCATTTTTGGAGTGG[C/T]AAGAAATTATTTGTT | 84959 |
rs1894083 | snp | G/T | 0 | 0 | | | GRCh38.p7 | 11:122809028 | AAAAATATTTTCCAT[G/T]GGGTCCAAGTATAAT | 84959 |
rs1894084 | snp | A/G | 0.465996 | 0.12588 | | | GRCh38.p7 | 11:122733858 | TTACAGCAGATTTGA[A/G]CAGTCAAAATTTAAT | 84959 |
rs1894085 | snp | G/T | | | | | GRCh38.p7 | 11:122733897 | TCtttttttttgttt[G/T]gtttttgagacagag | 84959 |
rs1894086 | snp | A/T | 0.497445 | 0.0356514 | | | GRCh38.p7 | 11:122740072 | TGATTCCATTTTGTC[A/T]TATTCATTTAATAAA | 84959 |
rs1894087 | snp | A/G | 0.47852 | 0.101384 | | | GRCh38.p7 | 11:122740152 | TATTCAGTTCTACAC[A/G]CTGAAGGATCCCATA | 84959 |
rs1894088 | snp | A/G | 0.159622 | 0.233092 | | | GRCh38.p7 | 11:122741020 | TTCAAAGCGCATATT[A/G]ACATATAAATGAATT | 84959 |
rs1894089 | snp | A/C | 0 | 0 | | | GRCh38.p7 | 11:122774330 | CTGCGCACAGATACC[A/C]AATGATCAGGATAAG | 84959 |
rs1945394 | snp | C/T | 0.342806 | 0.232136 | utr-variant-3-prime | UBASH3B | GRCh38.p7 | 11:122813889 | GAAAAAGATTGTAAA[C/T]GCAGATGAAATAACT | 84959 |
rs1945395 | snp | C/T | 0.151001 | 0.229563 | intron-variant | UBASH3B | GRCh38.p7 | 11:122722591 | AAAAGAAGCCCAATT[C/T]TCTACCAAGCTGGAG | 84959 |
rs1945396 | snp | C/G | 0.0770498 | 0.180522 | intron-variant | UBASH3B | GRCh38.p7 | 11:122727727 | CTGGTTTCTTAGGTA[C/G]AGCATAAGGCTGTTT | 84959 |
rs1945397 | snp | A/G | 0.376195 | 0.215812 | intron-variant | UBASH3B | GRCh38.p7 | 11:122727894 | CCGCACAGCTGGGCC[A/G]GATGGCAGCAGTGGC | 84959 |
rs1945398 | snp | A/G | 0.194902 | 0.243853 | intron-variant | UBASH3B | GRCh38.p7 | 11:122728076 | CTACGGGGCTCAAGC[A/G]GTCTTCCTGCCTCAG | 84959 |
rs1945401 | snp | G/T | | | intron-variant | UBASH3B | GRCh38.p7 | 11:122777596 | GGAAATGGCTTTCCC[G/T]GTCTATAAACTGCCT | 84959 |
rs1974428 | snp | A/T | | | intron-variant | UBASH3B | GRCh38.p7 | 11:122753197 | ctcggcctcccaaaa[A/T]gctggggttacaggc | 84959 |
rs1981408 | snp | C/T | 0.499784 | 0.0103811 | intron-variant | UBASH3B | GRCh38.p7 | 11:122767935 | TTAATGATGTCTCTG[C/T]GTTTATTTGGACCTT | 84959 |
rs1984602 | snp | C/T | 0.171704 | 0.237423 | intron-variant | UBASH3B | GRCh38.p7 | 11:122753961 | cattcggctggacat[C/T]gctgCACTAGGAGTT | 84959 |
rs1996841 | snp | C/T | 0.399073 | 0.200692 | utr-variant-3-prime | UBASH3B | GRCh38.p7 | 11:122811403 | AGTTGTAGTTTCAAA[C/T]GCAAGCATAGATGTA | 84959 |
rs2016174 | snp | C/T | 0 | 0 | intron-variant | UBASH3B | GRCh38.p7 | 11:122697549 | AGTCACTAGAAATCT[C/T]TGGAACTCTATTTGC | 84959 |
rs2040318 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UBASH3B | GRCh38.p7 | 11:122684639 | cctgggcaacaagag[C/T]gaaactctgtctcaa | 84959 |
rs2040319 | snp | A/C | 0 | 0 | intron-variant | UBASH3B | GRCh38.p7 | 11:122765344 | CAGTGAGAAGTGGCC[A/C]ATAAGCCTCTCCTTA | 84959 |
rs2040320 | snp | C/G | 0.175254 | 0.238565 | intron-variant | UBASH3B | GRCh38.p7 | 11:122765253 | TTGGCATTAGAGGAA[C/G]TTGAGGATATTGAAA | 84959 |
rs2156801 | snp | C/T | 0.495407 | 0.0477027 | intron-variant | UBASH3B | GRCh38.p7 | 11:122783348 | ACAATCCTGAGCCAA[C/T]GGACTCTCTGTTAGG | 84959 |
rs2156802 | snp | A/G | 0.238536 | 0.249737 | intron-variant | UBASH3B | GRCh38.p7 | 11:122783242 | ACCTGGTAGCTTCTG[A/G]AACCACAGTGAGACA | 84959 |
rs2156803 | snp | A/C | | | intron-variant | UBASH3B | GRCh38.p7 | 11:122661873 | CCaaaaaaaaaaaaa[A/C]caaaaaaaaaaaTAC | 84959 |
rs2156804 | snp | G/T | 0.454423 | 0.143914 | intron-variant | UBASH3B | GRCh38.p7 | 11:122739618 | AGGAGACATAAATTT[G/T]CTTCCTAACTTTGCA | 84959 |
rs2156805 | snp | A/G | 0.472241 | 0.114494 | intron-variant | UBASH3B | GRCh38.p7 | 11:122739860 | GATAACACATCCTTC[A/G]GACAGATGGCACAGC | 84959 |
rs2187519 | snp | G/T | 0.377977 | 0.21476 | intron-variant | UBASH3B | GRCh38.p7 | 11:122714378 | CCTAAGGGCCAATAG[G/T]TAGCAATTTCAGGAA | 84959 |
rs2271719 | snp | A/G | 0.181978 | 0.240568 | intron-variant | UBASH3B | GRCh38.p7 | 11:122712293 | GAGGACTTTGAGGAC[A/G]ATATGGCCATCTGGT | 84959 |
rs2276408 | snp | C/T | 0.333361 | 0.235692 | intron-variant | UBASH3B | GRCh38.p7 | 11:122808203 | TCGTACTTTGGGGTC[C/T]GTGATGGCTAGTAGT | 84959 |
rs2282645 | snp | C/T | 0.14933 | 0.228835 | intron-variant | UBASH3B | GRCh38.p7 | 11:122765195 | TGTGCCCCTGACATT[C/T]ACCTTGGCTAAATCA | 84959 |
rs2370779 | snp | A/G | 0.4444 | 0.15719 | intron-variant | UBASH3B | GRCh38.p7 | 11:122788983 | GAGGGCGATGTGCCC[A/G]GGAGCCCTTGGGGTC | 84959 |
rs2370780 | snp | C/T | 0 | 0 | intron-variant | UBASH3B | GRCh38.p7 | 11:122788941 | AGTAGATGTGAATTC[C/T]TATCAGAGAGCACTT | 84959 |
rs2840376 | snp | C/T | 0.196149 | 0.244131 | intron-variant | UBASH3B | GRCh38.p7 | 11:122748761 | TTTGGGGTTGGTAGG[C/T]GCTTAGAGTTGGGTG | 84959 |
rs3031285 | in-del | -/AT | | | intron-variant | UBASH3B | GRCh38.p7 | 11:122768521 | tgtatatatatatat[-/AT]ttgagactgagcctc | 84959 |
rs3107637 | snp | C/G | 0.486595 | 0.0807641 | intron-variant | UBASH3B | GRCh38.p7 | 11:122809177 | TGAATCAGGAGAATC[C/G]CTTGAATCCAGGAGG | 84959 |
rs3134416 | snp | A/T | 0 | 0 | intron-variant | UBASH3B | GRCh38.p7 | 11:122806741 | CTATTCTTAATAACT[A/T]AAATTCTGCGTTATA | 84959 |
rs3134428 | snp | A/G | 0.472989 | 0.113031 | utr-variant-3-prime | UBASH3B | GRCh38.p7 | 11:122811448 | AAGAAGAGGACATGA[A/G]AGGATGCTGGCTATA | 84959 |
rs3134430 | snp | A/T | 0.472803 | 0.113397 | utr-variant-3-prime | UBASH3B | GRCh38.p7 | 11:122812674 | GGATTGAAAGCCTGA[A/T]AGCATTTCCTGCTTC | 84959 |
rs3134439 | snp | A/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | UBASH3B | GRCh38.p7 | 11:122813760 | TTAGGTGATAGCAGA[A/T]GCTTTTCATTTTTAA | 84959 |
rs3737526 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | UBASH3B | GRCh38.p7 | 11:122806614 | ACTTGCTTTGGCTAA[C/T]CAAAGAAATGTATTT | 84959 |
rs3741015 | snp | A/T | 0.0420149 | 0.138716 | synonymous-codon | UBASH3B | GRCh38.p7 | 11:122801255 | TAATGTGCTCCCAGC[A/T]ACCCATTTTGTCCAC | 84959 |
rs3819248 | snp | C/T | 0.320575 | 0.239832 | intron-variant | UBASH3B | GRCh38.p7 | 11:122806339 | GCCTTGAAATAAAAG[C/T]TTAGAGTGATATCTT | 84959 |
rs3892187 | snp | A/G | 0.498034 | 0.0312882 | intron-variant | UBASH3B | GRCh38.p7 | 11:122795493 | CTTACAGCTGTTTCT[A/G]CATTCCGTCTTTCTG | 84959 |
rs3927805 | snp | A/C | | | intron-variant | UBASH3B | GRCh38.p7 | 11:122656444 | GGGCTGGTCTG[A/C] | 84959 |
rs3937026 | snp | G/T | 0.305436 | 0.243776 | upstream-variant-2KB | UBASH3B | GRCh38.p7 | 11:122655058 | TCCTCTACCCTCCTA[G/T]CCCTTCCTTCTTCTC | 84959 |
rs3937027 | snp | A/C | 0.304188 | 0.244057 | upstream-variant-2KB | UBASH3B | GRCh38.p7 | 11:122655065 | CCCTCCTAGCCCTTC[A/C]TTCTTCTCCTCCTCC | 84959 |
rs4016787 | snp | A/T | 0.258843 | 0.249844 | intron-variant | UBASH3B | GRCh38.p7 | 11:122714890 | atgacatgggtacta[A/T]aattgcactcacttt | 84959 |
rs4016788 | snp | A/C | 0.25801 | 0.249872 | intron-variant | UBASH3B | GRCh38.p7 | 11:122714865 | cactttacagatgag[A/C]gaaggagaaggtaaa | 84959 |
rs4016789 | snp | A/G | 0.495521 | 0.0471118 | intron-variant | UBASH3B | GRCh38.p7 | 11:122768508 | TGTGTGTGTGTGTGT[A/G]TATATATATATATTT | 84959 |