SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6569 | snp | G/T | 0.499673 | 0.0127754 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933271 | TAGAGGTGCTGCAGC[G/T]GCTCCTGCTCTCTGA | 10422 |
rs14254 | snp | A/G | | | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933281 | CCTGGACTGTTAGAG[A/G]TGCTGCAGCGGCTCC | 10422 |
rs872373 | snp | A/G | 0.336017 | 0.234736 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942379 | TTTAGGTTAGGCACA[A/G]TGGCTCATGCCTGTA | 10422 |
rs915236 | snp | A/G | 0.40595 | 0.195396 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948678 | CAGTGGCAGGGGAGC[A/G]GGGCAGACACAGCCA | 10422 |
rs1044191 | snp | A/G | 0 | 0 | missense | UBAC1 | GRCh38.p7 | 9:135945173 | CGCCTCTTCCTGGCC[A/G]AGCTCCCCCAGAGGC | 10422 |
rs1044193 | snp | A/G | 0.166632 | 0.23569 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135939721 | GGGGTTCGACGAGAA[A/G]GAGGTGATAGATGCC | 10422 |
rs1044239 | snp | A/C | | | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933074 | TTGCTTGGAGAGTCC[A/C]CTTGTTATTTGACGG | 10422 |
rs1810986 | snp | C/T | 0.28052 | 0.24813 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934477 | GAGACAGGGTTTTAC[C/T]GTATTAGCCAGGATG | 10422 |
rs2297688 | snp | C/G | 0.324145 | 0.238752 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948231 | GGGGCTCAGCTGCAG[C/G]CTGGGTGGTTCTTCT | 10422 |
rs2297689 | snp | A/G | 0.396546 | 0.202545 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948042 | CTCCAGGCTCCCCCA[A/G]CTCATCAAGGAGTTT | 10422 |
rs2297690 | snp | C/T | 0.312837 | 0.241974 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946459 | CTCAACTCTCAGAAT[C/T]AAGAGTTCTAGGACA | 10422 |
rs2297691 | snp | A/G | 0.335101 | 0.23507 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946112 | GCAACTCCTGTTGAT[A/G]TGCCTGAGGGCGGGC | 10422 |
rs2297692 | snp | C/T | 0.309894 | 0.242719 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944849 | TGGCGAGCCTGGGGG[C/T]GGTGGGCCTGGGGAC | 10422 |
rs4301514 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935294 | AACATTCAACAAAGG[A/C]AGATGTGCCTAATAT | 10422 |
rs4351484 | snp | A/G | 0.335559 | 0.234904 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935542 | cataactacccatga[A/G]gatgacttgagccca | 10422 |
rs4355852 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935739 | ataaccaaaaggaat[A/G]caagtggccaggcgc | 10422 |
rs4841900 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941676 | ACACCTGGCAGTCCC[C/T]GCCCTCCCTCCCAGC | 10422 |
rs4841901 | snp | A/T | 0.406296 | 0.19512 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959686 | CCCAGAGAAGTTTTT[A/T]AAAATACACACAACT | 10422 |
rs4841902 | snp | A/C | 0.498964 | 0.02274 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960280 | GAACTAGTTCCAAAA[A/C]TCAGCAACCTAAGGA | 10422 |
rs4842054 | snp | A/G | 0.316243 | 0.241064 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941361 | CAGTGAGCCAAGATC[A/G]CACCACTGTACTCCA | 10422 |
rs4842055 | snp | G/T | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945413 | AGGTGCGACGGAAGC[G/T]CTGGTCCTTGCCTCA | 10422 |
rs6537919 | snp | A/G | 0.336702 | 0.234484 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954000 | AAAAATTAGCCAGGC[A/G]TGGTGGCGCATGCCT | 10422 |
rs6537920 | snp | A/G | 0.49907 | 0.0215454 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958455 | ACCACGGTGATCCCA[A/G]TTTGCACAAAACAGA | 10422 |
rs6537921 | snp | C/T | 0.386504 | 0.209444 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961478 | GGGGCGCGCTGTGGC[C/T]ACCGCAAAGGAAGTG | 10422 |
rs6537922 | snp | C/T | 0.0275645 | 0.114116 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961540 | GCTGTAGTTCTCTGG[C/T]AGCTTCGTTCCTCCC | 10422 |
rs6537923 | snp | C/G | 0.0689305 | 0.172377 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961559 | TTCGTTCCTCCCCGA[C/G]CTGCAGGCGGTTCCC | 10422 |
rs7024472 | snp | A/G | 0.0707826 | 0.174302 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962538 | TAAGGCACAGTTCCC[A/G]TTCTCAGAGGTTAGC | 10422 |
rs7026477 | snp | C/T | 0.336702 | 0.234484 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950137 | cctgaacacagccct[C/T]cggcaccctgatttc | 10422 |
rs7028495 | snp | C/T | 0.0114815 | 0.0748929 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135946294 | CTTAAACAATTCCAC[C/T]GCATCTGGGTTCAGC | 10422 |
rs7029100 | snp | A/G | 0.397271 | 0.202018 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956424 | ACACGGGGGCTAGGC[A/G]CGTCGGCTCACCATT | 10422 |
rs7029359 | snp | A/C | 0.397452 | 0.201886 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955935 | TCACTAAGTAACAGC[A/C]ATGCTGCATCCCGAG | 10422 |
rs7030007 | snp | A/C | 0.396546 | 0.202545 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956394 | CTGGCTTGCGGGAGT[A/C]CTGCTTTCCTTTGAA | 10422 |
rs7848205 | snp | A/G | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954157 | AAAAAAAAAAAAAAA[A/G]AAGAAGAGCAGGGCT | 10422 |
rs7860947 | snp | C/G | 0.499137 | 0.0207489 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957463 | AAACCCACAGTCCAC[C/G]TGTCACCAGCACACC | 10422 |
rs7868264 | snp | A/G | 0.396182 | 0.202807 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958764 | TGACTAACGCATTCT[A/G]GCCCTGCCTGCAGAA | 10422 |
rs7870592 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947307 | CCGAGGCTGGAGTAC[A/G]ATGATGCAATCTCGG | 10422 |
rs7871519 | snp | C/G | 0.396727 | 0.202413 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947343 | TGCAACCTCCGCCTC[C/G]CGGGTTCAAGTGATT | 10422 |
rs10116480 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944609 | GCCTGAGCGGCCCCT[C/T]GCTCATGGACACCCC | 10422 |
rs10119464 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952778 | gggaatatttgcatt[C/T]caaataatcaactca | 10422 |
rs10122454 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944602 | GCTGGCAGCCTGAGC[A/G]GCCCCTCGCTCATGG | 10422 |
rs10448315 | snp | G/T | 0.286042 | 0.247388 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961917 | AGATCAGAGAGTCAC[G/T]GTTCCTGCGAAGCCT | 10422 |
rs10553564 | in-del | -/CTCA | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939504 | CACAGCCCACACTCA[-/CTCA]GCCCACACTCACTCA | 10422 |
rs10690817 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958050 | CAGGTATAATTTTCT[-/T]TTTTTTTTTTTTTTG | 10422 |
rs10735241 | snp | C/G | 0.084364 | 0.187256 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949143 | TTATGAGCCAGGACA[C/G]ACGGCCCACGGAGGA | 10422 |
rs10745377 | snp | A/C | 0.404559 | 0.196498 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935900 | GCACGGTGGCGGGCA[A/C]CTGTAGTCCCAGCTA | 10422 |
rs10745378 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937626 | AATGAGAGATTGTTT[A/G]AGGAGACACAAATAC | 10422 |
rs10776856 | snp | C/T | 0.496263 | 0.0430645 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945267 | TGCAAGGCAAGAGAC[C/T]CTTTCCAACATCCCC | 10422 |
rs10858184 | snp | C/T | 0.280256 | 0.248162 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937118 | GCTCCAGAGACACTT[C/T]CAGCCTGCTCGGGTG | 10422 |
rs10858185 | snp | A/G | 0.28052 | 0.24813 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937699 | GGCGACGGCCACACC[A/G]GAGGGAGGGATGAGG | 10422 |
rs10858186 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948905 | TGAAACCCCATCTCT[A/C]CTAAAAAGACAAAAA | 10422 |
rs10858187 | snp | A/G | 0.499563 | 0.0147699 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956777 | ACTCAGAGCTTGGAC[A/G]GAGAGAAGGCTGACT | 10422 |
rs10858188 | snp | A/C | 0.301177 | 0.244706 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960141 | GAGTCGCCACTAGAA[A/C]ATTGCAGCCTCCTTC | 10422 |
rs10858189 | snp | C/G | 0.28052 | 0.24813 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960239 | AGGCTTCTTAGCTGA[C/G]CTTACTGAGTCCTTT | 10422 |
rs10858190 | snp | C/T | 0.279461 | 0.248258 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960381 | GGACTTCTCTCTTGA[C/T]CAATTTTACCTCTGC | 10422 |
rs10858191 | snp | C/T | 0.284209 | 0.247648 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962454 | TAGTTCAGGTTAGAC[C/T]TGACACATTGACTGA | 10422 |
rs11103230 | snp | A/C | 0.278664 | 0.248351 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932692 | CGGTCATGTTTTTTA[A/C]AATGAAAAAAAAGGA | 10422 |
rs11103231 | snp | C/G | 0 | 0 | missense | UBAC1 | GRCh38.p7 | 9:135933496 | GCTGTTCAGTGGGTT[C/G]TCCAGCATGTCTTCA | 10422 |
rs11103232 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937249 | gagttcgagaccagc[C/T]tggcaaacatggtga | 10422 |
rs11103233 | snp | C/T | 0.499968 | 0.00399348 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937863 | CATCGAAGACCCTGA[C/T]GAGTAGTAAGAGCAA | 10422 |
rs11103234 | snp | A/G | 0.280256 | 0.248162 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938586 | AGTCCGCTTTTCTCT[A/G]CAGACCCTGGTGTCG | 10422 |
rs11103235 | snp | A/C | 0.334871 | 0.235153 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942816 | ATGTCTACACACAGA[A/C]AGAACGTGCGCCTTG | 10422 |
rs11103237 | snp | C/T | 0.279195 | 0.248289 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953079 | AGGCGGACAGCAGCG[C/T]GGGAGTGAACCGTCA | 10422 |
rs11103238 | snp | A/C | 0.366266 | 0.221319 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960368 | GACCCTACTCCTGGG[A/C]CTTCTCTCTTGACCA | 10422 |
rs11405597 | in-del | -/C | 0.336017 | 0.234736 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932735 | GGTAGGCGGAGGCAG[-/C]CCGTGCTTGGGCTCA | 10422 |
rs11435128 | in-del | -/A | 0.499451 | 0.0165644 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940280 | TTAGAAAAAAAAAAA[-/A]TCCTAGGGCCGGGCG | 10422 |
rs11542895 | snp | G/T | 0.00873346 | 0.0655016 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933361 | TCGGGCCGCACCAGG[G/T]GGCTGCTGTGGCCTG | 10422 |
rs11791688 | snp | C/T | 0.00975586 | 0.0691575 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938720 | CCTGTGGTCCTGTTA[C/T]GGGCAGTCAGCAGTG | 10422 |
rs12115351 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952476 | CGCCACTTGCAGAAC[A/G]CATCTTCCTCTGCTC | 10422 |
rs12345224 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945381 | GTGACCCTTATAACA[A/T]GAACCTGAATGAACA | 10422 |
rs12352445 | snp | C/T | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934706 | CTCAGAAAGAACAAA[C/T]TATAAGGTGCGAAAC | 10422 |
rs12380316 | snp | C/T | 0.298905 | 0.24517 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959133 | ATCATGATGGCCATG[C/T]ACATCGCACCGAGTG | 10422 |
rs12380331 | snp | C/G | 0.299411 | 0.245069 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959229 | ATATTTTTGTCTATT[C/G]CATTAACCCACAAGT | 10422 |
rs12552793 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959415 | gagtcttgctctgtc[A/G]ccaggctggagtgca | 10422 |
rs12554408 | snp | C/G | 0.281313 | 0.248031 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944520 | GGGGAGATGAGGCGC[C/G]GGCGAGGAAGGTCCA | 10422 |
rs28757690 | snp | A/C/G | 0.0149611 | 0.0851875 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945157 | TGCTGTGGCCCCCTC[A/C/G]GCCTCTGGGGGAGCT | 10422 |
rs34017249 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935801 | GAGGCCGAGACGGGC[-/T]GGATCACGAGGTCAG | 10422 |
rs34065736 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950270 | TGTGTGGCGATTTGT[C/T]AGGTGGCAACGGAAA | 10422 |
rs34292104 | in-del | -/T | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959393 | GGGTTTTTTGTCTGG[-/T]TTTTTTTTTTTTTTT | 10422 |
rs34386340 | in-del | -/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947166 | CCTGCCCTGCCTGCT[-/G]GCGGCGTCCACGTGA | 10422 |
rs34581200 | in-del | -/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947746 | CCCCCCCACAGCAAT[-/C]CCCCCACACGGGGAC | 10422 |
rs34640525 | in-del | -/A | 0.0685596 | 0.171987 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960591 | TCAAAGATGCTGCTG[-/A]AAAAAAACCTCACCC | 10422 |
rs34729162 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935894 | GCCGGGCACGGTGGC[-/T]GGGCACCTGTAGTCC | 10422 |
rs34773979 | in-del | -/CAG | 0.300421 | 0.244863 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959333 | GGCTCAGGGAGGACA[-/CAG]CAGCACCTCAGAGAA | 10422 |
rs34795677 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957330 | TGGCTCTGCTCCCTG[-/A]AAATACTGGGGGTGC | 10422 |
rs34895090 | in-del | -/C | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961823 | GCTGTGATATTTCTT[-/C]TTGCACTGCACTGCT | 10422 |
rs35005080 | snp | C/T | 0.0413956 | 0.137783 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135938235 | ACCTAGCAATGTTTT[C/T]GGGTTGGTCAGGCCC | 10422 |
rs35360444 | in-del | -/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942060 | GGAGGGAATGGCAAT[-/G]GGGGAAGATCTTAGG | 10422 |
rs35492042 | in-del | -/AC | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959330 | ACTGGCTCAGGGAGG[-/AC]ACACAGCACCTCAGA | 10422 |
rs35653463 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942650 | GAGTGAAACTGTCTC[-/A]AAAAAAAAAAAAAAA | 10422 |
rs35679979 | snp | A/G | 0.301429 | 0.244653 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960943 | GGACCCCAGGTCGGG[A/G]CGGTTCGGGGACTGA | 10422 |
rs35719015 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942122 | GCATCCATATTTAAC[-/A]AAAAGGCTTAAGATG | 10422 |
rs35803292 | in-del | -/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135955221 | CCTGTGGGTGGACCA[-/C]CCCCCTCCTGGCTCC | 10422 |
rs35897611 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947237 | ACCCAAAATAACTCA[C/T]GGGTTCAGATTTGTG | 10422 |
rs35925532 | snp | C/T | 0.395087 | 0.203592 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939515 | CTCACTCAGCCCACA[C/T]TCACTCATCACAGCC | 10422 |
rs36016562 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947172 | CTGCCTGCTGCGGCG[-/T]TCCACGTGAGCACTG | 10422 |
rs36068848 | snp | C/T | 0.00103819 | 0.02276 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135938262 | GCCCAGCTGCACCAC[C/T]GGGTTATCCAGGATG | 10422 |
rs55907616 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937302 | AAAAATTAGCCAGGC[A/G]TGGTAGTGCACGCCT | 10422 |
rs55984832 | snp | C/T | 0.00790225 | 0.0623593 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947778 | CCATGCACCCGCCGC[C/T]GCTCTGGGCTGACAC | 10422 |
rs56142900 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957791 | TTTTTTTTTTTTTTT[-/T]AAAGACAGGGTCTCA | 10422 |
rs57527185 | in-del | -/A | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937441 | AAAAAAAAAAAAAAA[-/A]TCAGGAGTGGCACCA | 10422 |