SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13348 | snp | A/C | 0.489024 | 0.0732638 | utr-variant-3-prime, nc-transcript-variant | UBA6 | GRCh38.p7 | 4:67617773 | TTAACCATAGGAAGT[A/C]ATTTCCCTCTAGCTC | 55236 |
rs354861 | snp | A/G | 0.322959 | 0.239117 | intron-variant | UBA6 | GRCh38.p7 | 4:67634723 | TAAGATTCATGTTTG[A/G]CATTACATAGCTATT | 55236 |
rs354862 | snp | A/T | 0.322721 | 0.23919 | intron-variant | UBA6 | GRCh38.p7 | 4:67634045 | TGGAATTGTCGATAT[A/T]TGAGCATGTTCGACT | 55236 |
rs354863 | snp | A/G | 0.322721 | 0.23919 | intron-variant | UBA6 | GRCh38.p7 | 4:67633174 | AGAAGTTTGTTCAGA[A/G]TAGAAGAAGCAAGAA | 55236 |
rs354864 | snp | A/G | 0.31503 | 0.241394 | intron-variant | UBA6 | GRCh38.p7 | 4:67632633 | GGTCTGTACTACTCA[A/G]TGTTACCACTTCCTT | 55236 |
rs354865 | snp | C/T | 0.322245 | 0.239334 | intron-variant | UBA6 | GRCh38.p7 | 4:67632620 | CAGTGTTACCACTTC[C/T]TTACCCAGTAAATTT | 55236 |
rs354866 | snp | C/T | 0.200182 | 0.244986 | intron-variant | UBA6 | GRCh38.p7 | 4:67630362 | TTGTTATAAGAATCA[C/T]TCTTTTTGATACAGA | 55236 |
rs354867 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | UBA6 | GRCh38.p7 | 4:67627846 | TTTTTTACATGTTCA[A/G]TATATGCCTTTCTTG | 55236 |
rs354868 | snp | C/T | 0.137187 | 0.223099 | intron-variant | UBA6 | GRCh38.p7 | 4:67636045 | ATAAATTCTCCCCTG[C/T]TAATATATCTGCTCT | 55236 |
rs354869 | snp | C/T | 0.161924 | 0.233971 | intron-variant | UBA6 | GRCh38.p7 | 4:67636382 | tccctctccctctcc[C/T]gctcccgctccccac | 55236 |
rs354870 | snp | A/G | 0.177824 | 0.239355 | intron-variant | UBA6 | GRCh38.p7 | 4:67637272 | cctggagggaggtgg[A/G]gggcagcccctgccc | 55236 |
rs354871 | snp | G/T | 0.0494327 | 0.149241 | intron-variant | UBA6 | GRCh38.p7 | 4:67658236 | actataaagacaaat[G/T]cacacgtatgtttat | 55236 |
rs354872 | snp | C/T | 0.161924 | 0.233971 | intron-variant | UBA6 | GRCh38.p7 | 4:67649437 | ATTTTTGTCTTTGGA[C/T]TCTATATGTCACTCT | 55236 |
rs354873 | snp | A/G | 0.202651 | 0.245475 | intron-variant | UBA6 | GRCh38.p7 | 4:67652061 | aaattacaaaaatat[A/G]aattgtctagaagaa | 55236 |
rs354886 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | UBA6 | GRCh38.p7 | 4:67620025 | TGCCAGGCTCTGAAC[A/T]ATATCGATTTAATCC | 55236 |
rs354887 | snp | C/T | 0.21845 | 0.248001 | intron-variant | UBA6 | GRCh38.p7 | 4:67621263 | TTACTTTTTAAGGTA[C/T]AGATAATTCAGACTA | 55236 |
rs719391 | snp | C/G | 0.29278 | 0.246313 | intron-variant | UBA6 | GRCh38.p7 | 4:67645784 | CTGAAATTGTTTACT[C/G]TCTGACCCTTTACAG | 55236 |
rs1017878 | snp | A/C | 0.292266 | 0.246401 | intron-variant | UBA6 | GRCh38.p7 | 4:67670961 | CATTCCTCTTTCCTA[A/C]AATAACAAGTAAGAA | 55236 |
rs1017879 | snp | A/C/G | 0.310472 | 0.252507 | intron-variant | UBA6 | GRCh38.p7 | 4:67670931 | ATTCACTGCTGGACT[A/C/G]TTAAGCCAGAGTTAT | 55236 |
rs1017880 | snp | A/G | 0.301177 | 0.244706 | intron-variant | UBA6 | GRCh38.p7 | 4:67670771 | TACTAAAAGTACTGA[A/G]AATCTTTGATTCCTA | 55236 |
rs1038428 | snp | C/T | 0.301177 | 0.244706 | intron-variant | UBA6 | GRCh38.p7 | 4:67674053 | AGAGTCCATAAATAC[C/T]GCATAGGATATTAAG | 55236 |
rs1038429 | snp | A/G | 0.448452 | 0.152042 | intron-variant | UBA6 | GRCh38.p7 | 4:67673910 | TTGGAATGGAATTCC[A/G]TAGGATTATAACTTT | 55236 |
rs1048447 | snp | C/T | 0.259674 | 0.249813 | utr-variant-3-prime, nc-transcript-variant | UBA6 | GRCh38.p7 | 4:67617754 | TCCCTCTAGCTCCTT[C/T]CCTTCTACTCTCCTG | 55236 |
rs1057974 | snp | C/T | 0 | 0 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBA6 | GRCh38.p7 | 4:67618900 | CATAATACTATGGAT[C/T]TCTCTTTCATTAAGC | 55236 |
rs1057975 | snp | C/T | 0 | 0 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBA6 | GRCh38.p7 | 4:67618751 | CTGGAATGCTATTTA[C/T]AAAAGTTTTGTGTAT | 55236 |
rs1118524 | snp | C/G | 0.212728 | 0.247206 | intron-variant | UBA6 | GRCh38.p7 | 4:67661066 | atgtctgtaccctca[C/G]tgtatctaggaagta | 55236 |
rs1471732 | snp | A/G | 0.241627 | 0.24986 | intron-variant | UBA6 | GRCh38.p7 | 4:67697048 | tctcactctgttacc[A/G]agactggagtgcaga | 55236 |
rs1484184 | snp | G/T | 0.460027 | 0.135605 | intron-variant | UBA6 | GRCh38.p7 | 4:67634006 | AGCAATTCGTATGGT[G/T]CGAGCTAATAAAGAT | 55236 |
rs1487379 | snp | G/T | 0.0777841 | 0.181223 | intron-variant | UBA6 | GRCh38.p7 | 4:67635132 | CTGTCAACAAAGACA[G/T]AAAATTTTATTCACT | 55236 |
rs1487380 | snp | C/T | 0.257454 | 0.249889 | intron-variant | UBA6 | GRCh38.p7 | 4:67634010 | AAACAGCAATTCGTA[C/T]GGTGCGAGCTAATAA | 55236 |
rs1487381 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | UBA6 | GRCh38.p7 | 4:67633582 | GGTGAAAAAAGAAAA[A/G]CATAAAACACATGAG | 55236 |
rs1565070 | snp | A/C | 0.235564 | 0.249583 | intron-variant | UBA6 | GRCh38.p7 | 4:67621296 | TCAGTTGAGGTTAAT[A/C]ATTCTTAAATTATGA | 55236 |
rs1872231 | snp | C/T | 0.137527 | 0.223271 | intron-variant, upstream-variant-2KB | UBA6, UBA6-AS1 | GRCh38.p7 | 4:67700749 | GACCAGAACTCGCTC[C/T]CGACCGGAGCCCCCC | 55236 |
rs1967036 | snp | C/T | 0.450985 | 0.148678 | intron-variant | UBA6 | GRCh38.p7 | 4:67698820 | caaaaattagccaga[C/T]gtagtagcaggcgcc | 55236 |
rs1967037 | snp | A/C | 0.301177 | 0.244706 | intron-variant | UBA6 | GRCh38.p7 | 4:67698900 | gggaggaggaggctg[A/C]agtgagccaagatcc | 55236 |
rs2170870 | snp | C/G | 0.301177 | 0.244706 | intron-variant | UBA6 | GRCh38.p7 | 4:67649961 | GTTCTTGTACACAGA[C/G]GAGAGGACAGAGAAG | 55236 |
rs2170871 | snp | A/C | 0.446641 | 0.154377 | intron-variant | UBA6 | GRCh38.p7 | 4:67658876 | TAATTATAAAAAGGC[A/C]TGAGGGAACTTTTTT | 55236 |
rs2170872 | snp | A/G | 0.499942 | 0.00539106 | intron-variant | UBA6 | GRCh38.p7 | 4:67671248 | GGTGCATTACAGAAT[A/G]AGGATTTCTCTTTAT | 55236 |
rs2220136 | snp | A/C | 0.292266 | 0.246401 | intron-variant, upstream-variant-2KB | UBA6, UBA6-AS1 | GRCh38.p7 | 4:67699978 | GTTTTCCTTGCATGG[A/C]GGGGGCAATAGGCCT | 55236 |
rs2253287 | snp | C/T | 0.180702 | 0.240204 | intron-variant | UBA6 | GRCh38.p7 | 4:67671329 | TACGGTATAAGAACA[C/T]ATTAAAATAATTTAT | 55236 |
rs2306809 | snp | A/T | 0.453209 | 0.145623 | intron-variant | UBA6 | GRCh38.p7 | 4:67626055 | AAAACCATGAATGAA[A/T]AGCTCTGTTTTTAAG | 55236 |
rs2627251 | snp | A/G | 0 | 0 | intron-variant | UBA6 | GRCh38.p7 | 4:67693821 | AAATGAGGATCCTTA[A/G]CCTCTTAATATCTCA | 55236 |
rs2627254 | snp | G/T | 0.49645 | 0.0419827 | intron-variant | UBA6 | GRCh38.p7 | 4:67690115 | TTACCTCAACTGTCT[G/T]TTCCTGTAATGCTCT | 55236 |
rs2627255 | snp | G/T | 0.332106 | 0.236133 | intron-variant | UBA6 | GRCh38.p7 | 4:67683793 | GAGCCACCACAACTG[G/T]CCTGGTACGTCCATT | 55236 |
rs2627256 | snp | G/T | 0.179744 | 0.239925 | intron-variant | UBA6 | GRCh38.p7 | 4:67682056 | GATAGTTTAAATAAC[G/T]TAACTTCATCCCCTT | 55236 |
rs2627257 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UBA6 | GRCh38.p7 | 4:67677516 | TAACCTAGTGTATTG[A/T]GAAACAGAACAAAAA | 55236 |
rs2711141 | snp | A/G | | | intron-variant | UBA6 | GRCh38.p7 | 4:67691727 | tgcagacctcagtct[A/G]cagtacataatcaag | 55236 |
rs2711142 | snp | C/G | 0.0494327 | 0.149241 | intron-variant | UBA6 | GRCh38.p7 | 4:67691616 | TGGGTCCCATGATGT[C/G]ATTCAAGGTTTACAG | 55236 |
rs2711145 | snp | A/G | 0.496416 | 0.0421803 | intron-variant | UBA6 | GRCh38.p7 | 4:67679443 | AATCCAAAGCAAAAC[A/G]AATACATGGACTAAA | 55236 |
rs2711146 | snp | A/G | 0.202343 | 0.245416 | intron-variant | UBA6 | GRCh38.p7 | 4:67685453 | ggatgaatcataccc[A/G]atttagatgagactg | 55236 |
rs3032668 | in-del | -/ATTC | | | intron-variant | UBA6 | GRCh38.p7 | 4:67641991 | CCGACTATATTCCAC[-/ATTC]ATTTTCTTTTAGTTG | 55236 |
rs3033611 | in-del | -/AT | 0 | 0 | intron-variant | UBA6 | GRCh38.p7 | 4:67667567 | TATAAACTAAATACA[-/AT]GTTATATTTTCAAAT | 55236 |
rs3063097 | in-del | -/TCC | | | intron-variant, upstream-variant-2KB | UBA6, UBA6-AS1 | GRCh38.p7 | 4:67700541 | CTGGCTTTTTTTTTT[-/TCC]TTCTTCCGAAGTCAA | 55236 |
rs3188451 | snp | G/T | 0.454904 | 0.143228 | utr-variant-3-prime, nc-transcript-variant | UBA6 | GRCh38.p7 | 4:67618045 | TTTTGTGTTTTTTTT[G/T]TTTTTTTTTTTTAAA | 55236 |
rs3775880 | snp | A/G | 0.259397 | 0.249823 | intron-variant | UBA6 | GRCh38.p7 | 4:67640412 | ACATTACTAAGCTTA[A/G]TTTACTAAGACTTGC | 55236 |
rs3796715 | snp | C/T | 0.26271 | 0.249677 | intron-variant | UBA6 | GRCh38.p7 | 4:67627358 | CCATACCTGAAACTT[C/T]GGTGTGAGCTCCTTT | 55236 |
rs3796716 | snp | C/T | 0.449473 | 0.150701 | intron-variant | UBA6 | GRCh38.p7 | 4:67627395 | TTGTGAAAAAGCCCA[C/T]AGTTCATGTTAAAAC | 55236 |
rs3806809 | snp | A/G | 0.346147 | 0.230772 | intron-variant | UBA6 | GRCh38.p7 | 4:67639233 | TCTCATTATATATGT[A/G]TGGACTATGACTGAA | 55236 |
rs3816820 | snp | A/C | 6.58812e-05 | 0.00573901 | intron-variant | UBA6 | GRCh38.p7 | 4:67626499 | TGATAACATTAATAA[A/C]AATATATTCATATAT | 55236 |
rs3830312 | in-del | -/T | 0.216797 | 0.248176 | intron-variant | UBA6 | GRCh38.p7 | 4:67623289 | ACTTCTGAAAGTGGG[-/T]TTTTTTTTGTGTGTG | 55236 |
rs3849642 | snp | C/T | 0.308613 | 0.243032 | intron-variant | UBA6 | GRCh38.p7 | 4:67649021 | ATAATATGTAACACA[C/T]TCCATTTCACGAGTA | 55236 |
rs3860688 | snp | A/G | 0.429388 | 0.174127 | intron-variant | UBA6 | GRCh38.p7 | 4:67620749 | TACTTCTTACATGCC[A/G]TTACACTATTAGCCC | 55236 |
rs4058361 | in-del | -/CACA | 0.5 | 0 | intron-variant | UBA6 | GRCh38.p7 | 4:67696528 | ACACACACACACACA[-/CACA]TATAATTCTGCATAG | 55236 |
rs4058464 | in-del | -/CCATGA/CCATGATT | | | intron-variant | UBA6 | GRCh38.p7 | 4:67670840 | TCATCTTTATAAATT[-/CCATGA/CCATGATT]NNNNNNNTTTAAATA | 55236 |
rs4131908 | snp | A/G | 0.21725 | 0.247846 | intron-variant | UBA6 | GRCh38.p7 | 4:67659638 | atatataaaatACAT[A/G]TATTTTATATAGCAT | 55236 |
rs4146407 | snp | A/G | 0.245346 | 0.249957 | intron-variant | UBA6 | GRCh38.p7 | 4:67631615 | ATTTAACATTAAAGA[A/G]CCTAAGGTTTTCACT | 55236 |
rs4860853 | snp | G/T | 0.309154 | 0.242901 | utr-variant-3-prime, nc-transcript-variant | UBA6 | GRCh38.p7 | 4:67616215 | TGAATCTATGAAAAG[G/T]AAAATCGCTAAATCC | 55236 |
rs4860854 | snp | G/T | 0.321534 | 0.247249 | intron-variant | UBA6 | GRCh38.p7 | 4:67624379 | GCAGCTATGGGACTA[G/T]AGTAATATAAATTTC | 55236 |
rs4860855 | snp | C/T | 0.077417 | 0.180873 | intron-variant | UBA6 | GRCh38.p7 | 4:67624667 | CTGAATCATTATGAA[C/T]AAAGATTAGGGAAGT | 55236 |
rs4860856 | snp | C/T | 0.375 | 0.216506 | intron-variant | UBA6 | GRCh38.p7 | 4:67659635 | ggaatatataaaata[C/T]aTATATTTTATATAG | 55236 |
rs4860858 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBA6 | GRCh38.p7 | 4:67683822 | tcacgcctataatcc[C/T]agcactttgggaggc | 55236 |
rs5859098 | in-del | -/AT | 0.447938 | 0.152711 | intron-variant | UBA6 | GRCh38.p7 | 4:67667566 | CTATAAACTAAATAC[-/AT]AGTTATATTTTCAAA | 55236 |
rs5859100 | in-del | -/A | 0.0498117 | 0.149749 | intron-variant | UBA6 | GRCh38.p7 | 4:67678144 | ATTATGTAAATATAT[-/A]AAAAAATTTGACAAA | 55236 |
rs6815097 | snp | G/T | 0.300673 | 0.244811 | upstream-variant-2KB, intron-variant | UBA6, UBA6-AS1 | GRCh38.p7 | 4:67702605 | ATTTGATAAAATATG[G/T]TGTGAATTATTTCAG | 55236 |
rs6819135 | snp | A/G | 0.450985 | 0.148678 | intron-variant | UBA6 | GRCh38.p7 | 4:67685338 | GCTTAAAAAACCCCA[A/G]TGGTTTTCTATTTCC | 55236 |
rs6819522 | snp | G/T | 0.448452 | 0.152042 | intron-variant | UBA6 | GRCh38.p7 | 4:67685521 | tttttactactggga[G/T]gtaataaaagtattt | 55236 |
rs6819987 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBA6 | GRCh38.p7 | 4:67685100 | AGAGAAAAAAACAAC[C/T]ATcagttccctgacc | 55236 |
rs6825264 | snp | A/G | 0.448323 | 0.15221 | intron-variant | UBA6 | GRCh38.p7 | 4:67652490 | acttctggtgagaat[A/G]caaaacggtacagct | 55236 |
rs6825409 | snp | C/T | 0.306182 | 0.243605 | intron-variant | UBA6 | GRCh38.p7 | 4:67698687 | TAAATGGGATgggcg[C/T]ggtggctcatgcttg | 55236 |
rs6825921 | snp | A/C | 0.241627 | 0.24986 | intron-variant | UBA6 | GRCh38.p7 | 4:67638722 | CTCTGGCATGGTGAA[A/C]AGGTGAAAAGTACTC | 55236 |
rs6830861 | snp | A/G | 0.448452 | 0.152042 | intron-variant | UBA6 | GRCh38.p7 | 4:67660046 | tctaagcagcaaagc[A/G]ttcaaggggtgactt | 55236 |
rs6839447 | snp | C/T | 0.24134 | 0.24985 | intron-variant | UBA6 | GRCh38.p7 | 4:67663423 | TAAATGATCTAATCC[C/T]CTTTCCTTATTAAAA | 55236 |
rs6840867 | snp | A/G | 0.261608 | 0.24973 | intron-variant | UBA6 | GRCh38.p7 | 4:67649336 | CAGTTCCCCTACTAA[A/G]TATCTCTAAAAATGT | 55236 |
rs6841385 | snp | A/G | 0.300673 | 0.244811 | upstream-variant-2KB, intron-variant | UBA6, UBA6-AS1 | GRCh38.p7 | 4:67702556 | AAAAAATAAATACAG[A/G]AAACGATGCATCTTA | 55236 |
rs6841553 | snp | A/G | | | intron-variant | UBA6 | GRCh38.p7 | 4:67676110 | ctcactgcaacttcc[A/G]cctcccgggttcaag | 55236 |
rs6845248 | snp | A/G | 0.301177 | 0.244706 | intron-variant | UBA6 | GRCh38.p7 | 4:67685197 | ttaatatttactccc[A/G]tatttctaaataaca | 55236 |
rs6845645 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | UBA6 | GRCh38.p7 | 4:67685411 | AACTAGTCCCTGCTT[A/T]GTTCTCTAGTGTCAT | 55236 |
rs6847079 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBA6 | GRCh38.p7 | 4:67682406 | aaaatcagataattt[A/G]gcaccacaatccata | 55236 |
rs6849445 | snp | C/T | 0.301177 | 0.244706 | intron-variant | UBA6 | GRCh38.p7 | 4:67659964 | tggtggcattttgcc[C/T]ctgccctagagatct | 55236 |
rs6851421 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBA6 | GRCh38.p7 | 4:67685635 | ttaaaccccgttacg[C/T]aggacctaatgggag | 55236 |
rs6852726 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBA6 | GRCh38.p7 | 4:67695232 | GATTAAGAATCCCAA[C/T]GTAAGAGTCccactc | 55236 |
rs6857476 | snp | A/G | 0.292266 | 0.246401 | intron-variant | UBA6 | GRCh38.p7 | 4:67641757 | TAAGAATTGTCTACC[A/G]CAGTTTTCATGATCC | 55236 |
rs6858851 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA6 | GRCh38.p7 | 4:67648937 | AGTGTTGGAGGCATA[C/T]TGCTTGCATCTCTTT | 55236 |
rs7657559 | snp | C/T | 0.261608 | 0.24973 | intron-variant | UBA6 | GRCh38.p7 | 4:67684553 | TCACAATCTGTGTAA[C/T]TCTTTAATATTTGAG | 55236 |
rs7657708 | snp | C/T | 0.448452 | 0.152042 | intron-variant, upstream-variant-2KB | UBA6, UBA6-AS1 | GRCh38.p7 | 4:67699752 | GACTACAGGCGTGCA[C/T]CACCTACGCCCAGCT | 55236 |
rs7657950 | snp | A/G | 0.448452 | 0.152042 | intron-variant | UBA6 | GRCh38.p7 | 4:67675963 | CTCTAGATTTGTTTA[A/G]TTTTGTTTTTGTCTG | 55236 |
rs7660012 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | UBA6 | GRCh38.p7 | 4:67679823 | AGTATTTACTCATTA[C/T]GAACGTTCTAGCTCT | 55236 |
rs7660038 | snp | C/T | 0.451234 | 0.14834 | intron-variant | UBA6 | GRCh38.p7 | 4:67679865 | AGACTTTGTAAACAG[C/T]GACAaagactactgg | 55236 |
rs7660874 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | UBA6 | GRCh38.p7 | 4:67658304 | aggtagggtaggtat[A/G]taagagaaacaaaga | 55236 |
rs7667814 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBA6 | GRCh38.p7 | 4:67631594 | TAAATGAACAGGGAT[A/G]AAATAATTTAACATT | 55236 |