SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs142667765 | in-del | -/TTG | 0.0360663 | 0.129354 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163602 | AGCTGGTTTTCAATC[-/TTG]TTCTCATCAGGACAC | 219333 |
rs142691067 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143028 | AACTGGGGAGGCGGA[A/G]GTTGCAGTGAGCCAA | 219333 |
rs142710874 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146432 | TGTAATAACGCACAC[C/G]GCTAAAGGCTAGGGG | 219333 |
rs142801243 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157928 | AAGCCCTTTGGAACT[C/T]AAACAGCTTTGAATC | 219333 |
rs142811180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27081375 | TTTGATCTTCCATAA[C/G]AAGCAACTTCTCATT | 219333 |
rs142824608 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137481 | GCTCACCATCAAAAA[C/T]GAATTTTAAAGTGCT | 219333 |
rs142849383 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132777 | AGTGCTATGTATGAG[C/T]TCTTCTCTGCTCTCT | 219333 |
rs142851413 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP12 | GRCh38.p7 | 13:27084374 | AGCTGGGCATGGTGG[C/T]GCACACCTGTAGTCC | 219333 |
rs142868634 | snp | C/T | 3.34622e-05 | 0.00409023 | synonymous-codon | USP12 | GRCh38.p7 | 13:27095664 | AATCTCATGAACCCA[C/T]GTTGGGTCTGGTGTG | 219333 |
rs142935250 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP12 | GRCh38.p7 | 13:27086390 | GAAAAAGTTTCGAAC[C/T]TGTACATAAAGTTTG | 219333 |
rs142982308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161845 | CGAGACTGCACCACT[A/G]CACTCCAGCCTGGGC | 219333 |
rs143018648 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27088959 | AGAAAAACACTGTAA[A/G]ATTCCTGTCCAAGAT | 219333 |
rs143022152 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167244 | TCCAGCCTGGGCAAC[A/C]AGAGTGAAACTCCGT | 219333 |
rs143075992 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166505 | ATGTGACATCATCTC[A/G]CTGCAACTGGCCAAC | 219333 |
rs143113553 | in-del | -/A | 0.108275 | 0.205947 | intron-variant | USP12 | GRCh38.p7 | 13:27103413 | AAATGCTTTTCTATT[-/A]AAAAAAATGGCTTTT | 219333 |
rs143134312 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27106429 | GCGGGGAAATAAACC[-/C]TACTTTATAAAGTAA | 219333 |
rs143137464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27087666 | CTAAGAGAAACCAGG[A/G]CTCCTTGGAGAAATG | 219333 |
rs143167919 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130541 | TCTCACACACACACA[A/C]AAAAAATCACAAAAC | 219333 |
rs143218327 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27097808 | ATATCACTACATGTT[A/G]AATATCCTTTATCTA | 219333 |
rs143230277 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068043 | AAGGACTTGTCTTTT[A/G]TATTCCCGGTCTACT | 219333 |
rs143251126 | in-del | -/ACTT | 0.0543475 | 0.155628 | intron-variant | USP12 | GRCh38.p7 | 13:27107526 | GAAATATCAACATAA[-/ACTT]ATAACTCTGAAAATG | 219333 |
rs143315146 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | USP12 | GRCh38.p7 | 13:27112144 | TCTGACCTTGGGAAA[C/T]TACTAAACTGTTGTT | 219333 |
rs143352968 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27071856 | TGACAAAGGTTTTAA[A/C]CTCTTCCAGTTTAAG | 219333 |
rs143417278 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119453 | ACCCTTCTGGATTTA[A/C]GAATCTTCACTTGCA | 219333 |
rs143450941 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123682 | CAGTTCCCCTGCACA[C/T]GCTCTCTTGCCTGCC | 219333 |
rs143526618 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067456 | CAAAACACCTCTAGC[C/T]AGGGTAAGGCTTTAG | 219333 |
rs143528657 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27116443 | ATTTTCCTTTAATAA[C/T]TTATGGAATGCATTC | 219333 |
rs143534527 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27172051 | CCCTCCGCGGCCCTT[A/G]TGCGCGAGCCGGGGA | 219333 |
rs143554407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128325 | GTCAAGCCTTCACAT[G/T]TGGCTTAACAATAAC | 219333 |
rs143591152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150266 | TGTATTTATATATGC[C/T]TGTCCTGAACAATCT | 219333 |
rs143642135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136938 | TTAACTAAAGCATGA[C/T]AGGTGCTTGGGGGTA | 219333 |
rs143661705 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP12 | GRCh38.p7 | 13:27093695 | CAAAGGAAGTAAAAA[C/T]TCACATCCACACAAA | 219333 |
rs143675862 | in-del | -/T | 0.0410537 | 0.137264 | intron-variant | USP12 | GRCh38.p7 | 13:27109537 | TGACTTGAAAAAAGG[-/T]TGAAAAGGACTCAAG | 219333 |
rs143684242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27093613 | TGGAAGACAGAATGT[C/T]GGTTTCTTATCAAAC | 219333 |
rs143724773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151256 | GAATCATTTGAACAC[A/G]GGAGGTGGAGGTTGC | 219333 |
rs143730921 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27073491 | AGAGACTTAAGGATT[C/T]AAGGCTGGGGAAAGA | 219333 |
rs143748280 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141390 | AACCATGACACCTCT[A/G]TAGTAATGAGCACAC | 219333 |
rs143810095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125310 | TAAAAATTAGCTTTT[A/C]ATGATTACATATAAA | 219333 |
rs143845136 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | USP12 | GRCh38.p7 | 13:27079336 | TCTAAATTTCACCTC[A/C]GATTTCTCTTGACCA | 219333 |
rs143851729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138511 | ATGAGCAGCTTGACA[C/T]GCCTCAGACTTTCTT | 219333 |
rs143858321 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128841 | CTTCTATTTTTCCCA[C/G]CACCTATGTTACAGT | 219333 |
rs143939951 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134102 | TGAGCTATGATCAGG[C/T]CACTGCACTCCAGCC | 219333 |
rs143942050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27086740 | AGTTGTATTTCTCTT[A/G]GCTACATTTAGTCCC | 219333 |
rs143980932 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27069719 | GTGGGAGGCCAAGGC[A/G]GGCAGATCACCTGGG | 219333 |
rs143994862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27169733 | ACTGTCCTAATCTGA[C/T]TACAGCATACATTTA | 219333 |
rs144049396 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27114983 | GAATTAACCACTCTA[C/T]TAGCTCTGCTGCATC | 219333 |
rs144089775 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP12 | GRCh38.p7 | 13:27110337 | AACCAGATAAGTTCA[C/T]AGGGAAGACAGACAC | 219333 |
rs144098935 | in-del | -/G | 0.109814 | 0.206997 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164587 | AGCAAAGACTTACTA[-/G]TTTTTCTTCCTAAAT | 219333 |
rs144170369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106608 | ATATTTCTACTATGG[G/T]GTGAAATCAAGTATA | 219333 |
rs144174598 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153398 | TAGATAAAACATATA[C/T]ACATATGCATACAAA | 219333 |
rs144196797 | snp | C/T | 0.0225045 | 0.103662 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066217 | GCCTTCTTCAAGAAC[C/T]TTAAATGCTTTACAG | 219333 |
rs144205577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27111475 | AAGGTAGGTTTAAAT[C/T]AGGGAGAAGAAATTT | 219333 |
rs144280987 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27090775 | TGCAACAGGAGATAC[A/G]TCTGACTCAGCAACC | 219333 |
rs144284276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168130 | AGCACCTACCTTTAC[C/T]AGCTTTGGCCTCATT | 219333 |
rs144356487 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138610 | TGTTTTTGACTTTGC[C/T]GCGGGAAAGCCTTGG | 219333 |
rs144387368 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129872 | ACTGGCATGAAGCAC[A/G]GTCACATCCAAAACA | 219333 |
rs144421625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135640 | AAATTGTTTGAACCA[G/T]GGTGGCAAAGGTTGC | 219333 |
rs144428948 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | USP12 | GRCh38.p7 | 13:27070780 | CTGGTCTCAAACTCC[C/T]GACCTCAGGTGATCC | 219333 |
rs144443306 | in-del | -/AC | 0.0162398 | 0.0886349 | intron-variant | USP12 | GRCh38.p7 | 13:27075617 | ACACCACATAATTTG[-/AC]ACAGCACTCAATATG | 219333 |
rs144477155 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27077691 | ATTGAAATGGCTCCA[-/G]AAAAAAAGCAGAAAA | 219333 |
rs144575903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127815 | ATTAATCACTGCGCA[A/T]GTAACTGCAAATTTA | 219333 |
rs144581363 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27080345 | TGGAACTGGCTACAG[C/G]GGAATAAGATATGGA | 219333 |
rs144599280 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27085283 | CCTCCCAGGTTCAAG[C/G]AATTCTCTTGCCTTA | 219333 |
rs144602641 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161653 | TTTTGGGAGGCCAGC[C/T]ACATCACTTGAGTTT | 219333 |
rs144605958 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | USP12 | GRCh38.p7 | 13:27082971 | CTCCCGAGTTGCTGG[A/G]ATTATAGGCATGCGC | 219333 |
rs144642712 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27122139 | CCAACCTGGGCAACA[C/T]GGCGAAACCCCGTGA | 219333 |
rs144679913 | snp | A/G | 3.30398e-05 | 0.00406434 | synonymous-codon, intron-variant | USP12 | GRCh38.p7 | 13:27071128 | CTTAACTATTGCAAT[A/G]TAATGGCCTCGATTG | 219333 |
rs144704598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124326 | AAAAATGGTGTCTAT[A/G]AGGATATGTCATTTT | 219333 |
rs144733021 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129541 | GAAGGCTGGGCAACA[C/T]AGCAAGACTCTGTCT | 219333 |
rs144751630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27085446 | TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCG | 219333 |
rs144766365 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27081533 | AGTCATCAATGAGGG[C/T]TGGAATGAACTTCTT | 219333 |
rs144766540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158219 | GGCATAGAAGGAAGA[C/T]AAAATGGAGACAGAG | 219333 |
rs144837674 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134341 | CATTTGGCTTGCCAT[A/G]TAAGCTCATTCTCTA | 219333 |
rs144905332 | in-del | -/A | 0.0718919 | 0.175435 | intron-variant | USP12 | GRCh38.p7 | 13:27091163 | AGACAACTCAGAGAG[-/A]AAAAAAGAGGACATG | 219333 |
rs144935760 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131159 | CAGGAAGCAGTCAAT[A/G]TGGGAACTTGAGTGT | 219333 |
rs144951963 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145022 | CAGTGAGCCACGATC[A/G]CACCACTGCATTCCA | 219333 |
rs144977843 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067015 | CAATCCCTCCCCTGA[C/T]AAATCATACTATGAA | 219333 |
rs144978145 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143650 | TCCACTTGAATCAAA[A/T]CATCAAATTCAGCAT | 219333 |
rs145004904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27105559 | ATTAATTACTGTAAG[A/G]CTATCTCCTTCACTA | 219333 |
rs145069076 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140895 | ACTGAACTTCAGAAA[C/T]GTCACACAAGAATCT | 219333 |
rs145157323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27111484 | TTAAATTAGGGAGAA[A/G]AAATTTTAAAAGTTG | 219333 |
rs145176527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27100207 | ACCTTGCCCTTCAAT[A/G]CAATAATCCTCCGTC | 219333 |
rs145212931 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164127 | TCAGGTAGAGGCTTA[A/G]TAGGTCACTAAAATA | 219333 |
rs145263898 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153774 | ATAGCCCATACACCA[A/G]TATTTACTGGGTATT | 219333 |
rs145310848 | in-del | -/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144748 | TTTTGTTTTTTGTTG[-/T]TTTTTTTTTTTCCCC | 219333 |
rs145383229 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159848 | TGGCAAGAACATCAC[A/G]GTAGGCTATTAGCAC | 219333 |
rs145395067 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27083266 | ATAGTGCAAGAATTA[A/C]CAAAAATGTGACAGA | 219333 |
rs145418842 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158661 | CTAAACACATCTAAA[C/T]GTAGAAAAGGTACAG | 219333 |
rs145472128 | in-del | -/T | 0.0629771 | 0.165899 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161971 | AGGGTAATCTAAAAC[-/T]TTTGCTTCATGGATC | 219333 |
rs145491414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27122476 | AAACGGACTAATACA[C/T]CCCATCTTTACCGAA | 219333 |
rs145502374 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | USP12 | GRCh38.p7 | 13:27092622 | TCAACAGAGAAAGAA[C/T]TGTCTTTTAAACAAA | 219333 |
rs145554917 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP12 | GRCh38.p7 | 13:27118874 | TGTATTCTAACCACC[C/T]CACATGTCCACCTGT | 219333 |
rs145556847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162296 | AAAGTCACACACACA[C/T]AGATATGCAGCCGAA | 219333 |
rs145622126 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27108299 | CAAAAAACCAAACAC[C/T]GCATGTTCTTACTCA | 219333 |
rs145680445 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27072870 | TGAGGCTGCGCACAC[C/T]CTCCACACTTTCATA | 219333 |
rs145723589 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27103124 | AATATGGGGCTAATA[C/G/T]CTATTGAGAATAAAA | 219333 |
rs145857651 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163250 | ATGTGAATCAATACT[C/T]GGTAAACTCCTGGTA | 219333 |
rs145895038 | in-del | -/CAAA | 0.0547245 | 0.156101 | intron-variant | USP12 | GRCh38.p7 | 13:27102410 | GCCAAAGGGTCTTCT[-/CAAA]CAAATCAGAACGTAT | 219333 |
rs145920106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132622 | TCAAGAGGGTTTCCT[C/G]TGCATTTGCGTAGGT | 219333 |
rs145940698 | in-del | -/TA | 0.0829062 | 0.185956 | intron-variant | USP12 | GRCh38.p7 | 13:27169859 | GTCGCCTCTAGCACT[-/TA]TAGTGGCTGCTAAGT | 219333 |
rs145978304 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP12 | GRCh38.p7 | 13:27075986 | AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 219333 |
rs145985354 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | USP12 | GRCh38.p7 | 13:27116198 | GCGCCTGTAGTCCCA[C/G]CTACTCGGGAGGCTG | 219333 |
rs146024677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153410 | ATATACATATGCATA[C/T]AAAAACATATAAAGT | 219333 |
rs146035332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156592 | GGAAGCCAAGACAGG[C/T]GGATCACCTGAGGTC | 219333 |
rs146088120 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137697 | CCTGCTAGTATCCAT[G/T]CCTTTGTATAATTGC | 219333 |
rs146107525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133594 | ATATCGCGCCACTGC[A/G]CTCCAGCCTGCGACA | 219333 |
rs146130517 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172571 | ACCTGTTGGCCTGTT[A/G]GCGATAAATTTATAA | 219333 |
rs146212445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156120 | TCATTCTGACAATGC[C/T]AGCCTCATCATTATA | 219333 |
rs146214343 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128509 | ACTATATCTGAACTC[C/T]GTAACTGGCACCTTA | 219333 |
rs146234714 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27076241 | TATTAAGAAAAATGA[A/C]AATGTATATCCTAGA | 219333 |
rs146242061 | in-del | -/AAAAAAAATT | 0.466824 | 0.124448 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161900 | AAATAAAAAAAAATA[-/AAAAAAAATT]AAAAAGCCACTCATT | 219333 |
rs146245912 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27080732 | ATAAAGTGAGGACCG[A/C]AATAAAGTGAAGACC | 219333 |
rs146354441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27094661 | AGCCATGAATGCATA[A/G]CCTGCATCTAGTTAG | 219333 |
rs146366791 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27098124 | GTAAAGTTGTTACTA[C/T]CTCAGCCACCCCATG | 219333 |
rs146437471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27169758 | CATTTATTGTTTACC[C/T]GAATACTGTTTGTGT | 219333 |
rs146455241 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164495 | GAGAGGGCTATACCA[C/T]CTCACACAGTGGTGC | 219333 |
rs146521730 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27110645 | GTATGTGATTAAAGC[A/G]TACTGATATCAATGA | 219333 |
rs146629947 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127193 | TCATAGTTTTTAACT[A/G]TCCCATCAAAGTTAA | 219333 |
rs146652027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130845 | CAAGTCCAAAAAGAT[G/T]ACACAAGTATCACAA | 219333 |
rs146701049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128108 | GAACAAAAGAAGATT[C/T]GGATTTACCTTAAGT | 219333 |
rs146710757 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152057 | TACACTGTTGGCAGG[A/T]ACATAAAATGGTCCA | 219333 |
rs146748332 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144263 | AGTGCTTTGGGAGAC[C/G]AAGGTGGAAGCATCA | 219333 |
rs146760861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149600 | GGAGTAGAATAGTGG[C/T]TACTAGAGTAGAGGC | 219333 |
rs146766661 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27072041 | AATATCTTATGTTTC[C/T]CAGATCATTTGATCC | 219333 |
rs146777005 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | USP12 | GRCh38.p7 | 13:27078508 | TAACATAACAGGGGG[C/T]TGCCTTTCTTGATAA | 219333 |
rs146799992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150381 | TGACATATAAAAGAA[A/G]AAAACATTTCAGAGT | 219333 |
rs146822980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145042 | ACTGCATTCCAGCCT[A/G]GGCTGGACCCTGCAG | 219333 |
rs146877415 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | USP12 | GRCh38.p7 | 13:27086892 | TGGACAGAAACAGTG[A/G]GTAATCTGTTTTGAT | 219333 |
rs146887771 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27091120 | GACCTGAGTCTCAAA[A/T]AGTCTGGTGAAAAAG | 219333 |
rs146974671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27093136 | AGGAGGCAGAGGTTG[C/T]GGTGAGCCACTGCGC | 219333 |
rs146983012 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27078073 | TTCTATTTAAATTTA[-/T]TTTTTTAATGACATT | 219333 |
rs147007834 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132802 | CTCTCTCCACTCTCA[C/T]GCACTCCTCAGACAA | 219333 |
rs147018270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27088795 | TGTGTTTTGTATCCC[A/G]TCCCTGTAATAAATC | 219333 |
rs147078792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113511 | CCACCACGCTTCTTA[C/T]TCCAGCAGAGTAGAC | 219333 |
rs147111135 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152638 | TATATCTCAATAAAG[A/C]TGTTTTAAGAAAAAA | 219333 |
rs147120994 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | USP12 | GRCh38.p7 | 13:27109510 | AGATGACCTAGTTTC[C/T]CCACAAATTGATGAC | 219333 |
rs147121036 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155242 | GCGTGCCACCATGCC[C/T]GGCTAATTTTTTGTA | 219333 |
rs147132772 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | USP12 | GRCh38.p7 | 13:27109655 | GGGCGCAGTGGCTCA[A/G]GCCTGTAATCCCAGC | 219333 |
rs147142048 | snp | A/G | 0.0360663 | 0.129354 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27065806 | GAAAACAGATTTTAC[A/G]GGAGCAATTACTACA | 219333 |
rs147175352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27105600 | TCTTTGAAGAAAGGC[A/G]TGTCATCCTTGTTTC | 219333 |
rs147216458 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124938 | AGGAATCATAAAAAG[A/C]GTATCAAAGTAGTAG | 219333 |
rs147233227 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128998 | GTAACGGAGTTCATA[C/T]TCCAGATTCCATATG | 219333 |
rs147277032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125314 | AATTAGCTTTTCATG[A/C]TTACATATAAATAAA | 219333 |
rs147340283 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27099899 | GAGTTCTAAGAGCTC[C/T]GTACTAGCCTACATG | 219333 |
rs147340635 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146442 | CACACGGCTAAAGGC[C/T]AGGGGTATAAGGTAG | 219333 |
rs147383470 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143036 | AGGCGGAGGTTGCAG[C/T]GAGCCAAGATCACGC | 219333 |
rs147405786 | in-del | -/TG/TGTG/TGTGTG | 0.301137 | 0.278619 | intron-variant | USP12 | GRCh38.p7 | 13:27087099 | CAGAGGGGAAGGGGC[-/TG/TGTG/TGTGTG]TGTGTGTGTGTGTGT | 219333 |
rs147429188 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27085142 | TTTCTAATAGTATTA[A/T]AAATGGAATGTTTTC | 219333 |
rs147444897 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167258 | CAAGAGTGAAACTCC[A/G]TCTCAAAAAAAAAAT | 219333 |
rs147486925 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162131 | GTCTTACCAACAATG[A/T]CCATGTAAGGGTGAT | 219333 |
rs147534195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104739 | GATCCAGGCTTACCT[C/G]AATTCACTGTGTACA | 219333 |
rs147587567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27100222 | GCAATAATCCTCCGT[C/G]CCTGAAAATAATAAC | 219333 |
rs147604591 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27096694 | ATTCAAACTGGGCAG[A/C]CTGACTCCACCATGC | 219333 |
rs147692525 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP12 | GRCh38.p7 | 13:27122607 | CAGTGAGCCGGGAGT[A/G]TGCCACTACACCCCA | 219333 |
rs147702079 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27077892 | TTAGGGAGGTCTTGA[G/T]CACTGTCATTGTTTT | 219333 |
rs147708842 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP12 | GRCh38.p7 | 13:27119303 | GCCAATTCCATGAAG[C/T]GGCCCCCAGAGGTAT | 219333 |
rs147753738 | in-del | -/A | 0.0916144 | 0.193427 | intron-variant | USP12 | GRCh38.p7 | 13:27078025 | TAAACACTGATTTTT[-/A]AAAAATCTTCTGTAA | 219333 |
rs147792768 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138649 | AGTCAAACACTGGTC[A/G]TTATGACTGGTTTCA | 219333 |
rs147802085 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP12 | GRCh38.p7 | 13:27096079 | CAAAACCTATCCTTA[C/T]ATATTGGCATAACAG | 219333 |
rs147808822 | in-del | -/GAACCTGGGAGGCG | 0.0644693 | 0.167566 | intron-variant | USP12 | GRCh38.p7 | 13:27123011 | GCAGGAGAATGGCGT[-/GAACCTGGGAGGCG]GAGCTTGCAGTGAGC | 219333 |
rs147834771 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135852 | AGAAGGCAGCAAAGA[A/G]GGAAAACATGCTTTT | 219333 |
rs147878277 | in-del | -/G | 0.0908922 | 0.192833 | intron-variant | USP12 | GRCh38.p7 | 13:27078426 | ACCAACTGATACGGA[-/G]GCATAACTGTATGCA | 219333 |
rs147919743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27079058 | TTTCCAAATAAGCCA[C/T]AGGACAAACAGAACA | 219333 |
rs147940356 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154405 | ATTTTCCTGAATGTT[C/T]CACTGCATCTTTACT | 219333 |
rs147952536 | in-del | -/TT | 0.0170251 | 0.090679 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157668 | AACCTTATTTCTCTC[-/TT]GTTATTTTAATTCAC | 219333 |
rs148001162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27083419 | GCAATGTTCTGTTCT[C/T]TAAGACCTGAGCCTC | 219333 |
rs148097385 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27093859 | AAAATAAAGGAAATA[A/C]GTTATCAAGCCTTAA | 219333 |
rs148161238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27079963 | TAGAATGCTTTATGT[A/G]AGAAAGACACTAAGG | 219333 |
rs148169761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142414 | CATTACTGAGATAAC[C/T]GATTAAATTTTAAAA | 219333 |
rs148191332 | in-del | -/G | 0.0236746 | 0.106192 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165336 | ATTAGTGCTTTCTCA[-/G]GGGTATATACTACTA | 219333 |
rs148210885 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153302 | ACAGAGTGAGACTCC[A/G]TCTCAAAAAAAAATA | 219333 |
rs148257954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27087752 | CAGAAAGGAAAGAAA[C/T]ACTGGAGAATGACTG | 219333 |
rs148259751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166565 | TACTTTGAGACCTAT[C/T]AGCCACTTATTAGCA | 219333 |
rs148311914 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132937 | GCCAGCTATTCTGAA[C/T]GAACTTCTTTAATTA | 219333 |
rs148374673 | in-del | -/ATAT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148682 | AAAAAAAATTATATA[-/ATAT]TATATATATAATATA | 219333 |
rs148377693 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27104050 | TGAACTCTTTTTTTT[C/T]AGAGACAGGGTCTTG | 219333 |
rs148410282 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134403 | AGGAGAATAAGTCAG[C/T]AACTGAGAGGGTGGA | 219333 |
rs148420440 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP12 | GRCh38.p7 | 13:27116050 | GGGTGTGGTGGCTCA[C/T]GCCTCTAATCCCAGC | 219333 |
rs148430485 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27070939 | AGAAGTAGGAATTAG[A/G]CTACAATCTATAGAC | 219333 |
rs148483695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106417 | GGGGAGGGGGCGGGC[A/G]GGGAAATAAACCTAC | 219333 |
rs148522540 | in-del | -/AT | 0.0648419 | 0.167978 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068304 | ACAGGAATTTTTAAA[-/AT]AGTTTTTTAATTTTA | 219333 |
rs148525205 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27085969 | CCAGGAGATCTAGAT[A/G]AGCCTAGGCAACATA | 219333 |
rs148568003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129666 | AACTATGACCTGGGC[A/G]ACAGAGTGAGACCCT | 219333 |
rs148619778 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27095284 | AATTAATATGCCTCC[C/T]TGATCTGTATGATCC | 219333 |
rs148638769 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | USP12 | GRCh38.p7 | 13:27109890 | GCACTCCAGCCTGGG[C/T]GACACAGTGAGACTC | 219333 |
rs148661457 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143844 | AATTAAAAGACACCA[C/T]AAGGAAATGTTCAGA | 219333 |
rs148683774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156915 | TAACAGCATGATCCG[A/G]CGGCAAAAGCACTAG | 219333 |
rs148686057 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP12 | GRCh38.p7 | 13:27081199 | GATGCTGTTTGACAG[C/T]ATTTTATCCACAGAA | 219333 |
rs148699424 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27085161 | TGGAATGTTTTCTTT[C/T]TTCTTTCTTTCTTTC | 219333 |
rs148779889 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168508 | TCCCGTTATTTCACA[C/T]TTATTAAGTATAATA | 219333 |
rs148837487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128279 | TAGAAGTAACAGTAG[C/T]AATAATACTGGCTTT | 219333 |
rs148928568 | snp | C/G | 0.0912534 | 0.193131 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151155 | TCAACATGGCAAAAC[C/G]CCATCTCTACTAAAA | 219333 |
rs148933463 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136835 | AAGTAATAAAATGAT[A/G]TTTGGGATTTGCCCC | 219333 |
rs148957371 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP12 | GRCh38.p7 | 13:27073060 | CACTAAGACAGGGCT[A/G]GCAATGCACGTCTAG | 219333 |
rs148979424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27079220 | CTCCCTGTGTGGGGC[A/G]GGGGGGAGTGGGGGG | 219333 |
rs148995159 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27123486 | CAATACTAAGAATTT[A/G]TAGGCTGATATAGTT | 219333 |
rs149136492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27111660 | TAAGACCATTTTGAG[C/T]GCACATCCCTTACAC | 219333 |
rs149153250 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154189 | ATCTTTTAATGAAGC[C/T]GAACCATCATTTAAA | 219333 |
rs149205450 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158758 | ATAAAATTATTGTTT[A/C]ATAAAATGAAAATGT | 219333 |
rs149243845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27115426 | CACATCACTTCAACC[A/G]CTTTCCTCAAATCCA | 219333 |
rs149292352 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27121218 | GAGTAGAGACAGGGA[A/G]AAAGGAGAAACATCT | 219333 |
rs149312874 | snp | A/G | 0.000198131 | 0.00995119 | synonymous-codon, intron-variant | USP12 | GRCh38.p7 | 13:27071104 | AAACAACAACCAAAA[A/G]TCATGACTCTTAACT | 219333 |
rs149335490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161517 | TAGAAATAAAGGCAA[A/T]TTACTCACTATAATT | 219333 |
rs149388095 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129438 | CACTCTAAAGCTATG[C/T]GTAGGCCAGGTGCAG | 219333 |
rs149403504 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27109385 | TAAACTTTAATCAAG[C/T]CTCTACGTGTAACTA | 219333 |
rs149451338 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152968 | AAAAAAAGAAAGAAA[C/G]AAAAGAAAATAGAAT | 219333 |
rs149456980 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | USP12 | GRCh38.p7 | 13:27075704 | AACACACGTCTCTTA[A/T]AATAAGGCTAAATGC | 219333 |
rs149525098 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124677 | AATAAGAAAAGTTCT[A/G]GAGGCACAGGAAGCA | 219333 |
rs149555919 | in-del | -/CACATCCTAATCCCCAGAA | 0.0166325 | 0.0896639 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154703 | CTCCCTCAAAATGTC[-/CACATCCTAATCCCCAGAA]CCTGTGAATTCAAGT | 219333 |
rs149575226 | in-del | -/AT | 0.121717 | 0.214577 | intron-variant | USP12 | GRCh38.p7 | 13:27083858 | AACCTTTTTGGGAGA[-/AT]ATATATATATATATA | 219333 |
rs149599214 | snp | C/T | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167818 | ATTCCCAACAACGCA[C/T]GGGCTCTGAGGTTTG | 219333 |
rs149624642 | in-del | -/GG | 0.102726 | 0.202016 | intron-variant | USP12 | GRCh38.p7 | 13:27084581 | GATGACATAAGGTAA[-/GG]GGGTTCAACTTTATT | 219333 |
rs149672389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099512 | CTGCATGTCTAGTCT[A/G]TTCCATTTCCATTTA | 219333 |
rs149680428 | in-del | -/ACACAC/ACACACACACACAC/ACACACACACACACAC/ACACACACACACACACAC | 0.484491 | 0.0866827 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148795 | CAGAATCATCTTAAT[lengthTooLong]ACACACACACACACA | 219333 |
rs149714974 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148105 | CTGCACTCCAGACTG[A/G]GCAACAGAGCGAGAC | 219333 |
rs149767283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117467 | AGTCTAGATGGGCCA[C/T]TGTTAGGGAAATAGA | 219333 |
rs149777414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27072440 | AATGAGAGATGAAGG[A/G]CTGAACTTCCACCTA | 219333 |
rs149849006 | in-del | -/GCGTGTGCCTGCAGTCCCAGCCACTT | 0.0648419 | 0.167978 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141989 | GCGTGGTACATGATG[-/GCGTGTGCCTGCAGTCCCAGCCACTT]GCAAGGCTGAAGCAG | 219333 |
rs149859431 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162953 | TTAATTTTTTAACAT[A/G]TATATACAATCCAAA | 219333 |
rs149879406 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138455 | CCCTGTATCGCCCTC[C/T]AGAAAACACCTTTTA | 219333 |
rs149926076 | in-del | -/A | 0.0644693 | 0.167566 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146448 | CTAAAGGCTAGGGGT[-/A]ATAAGGTAGGGAGAG | 219333 |
rs149932492 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143441 | CTTTACAGAGGAATG[A/C]CTACTAATAAACATG | 219333 |
rs149975082 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153611 | AATGAAATGTTCAAC[C/G]TTTCCCCTTCCACAA | 219333 |
rs150031770 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27081834 | AGAGCTCTTGGGTGA[A/T]CACATGTATTGTCAA | 219333 |
rs150054920 | snp | C/T | 0.00220587 | 0.0331371 | missense, upstream-variant-2KB, utr-variant-5-prime | USP12, USP12-AS2 | GRCh38.p7 | 13:27171621 | AGGCGAATTTGGAGA[C/T]TGTCATTAGGATTTC | 219333 |
rs150074445 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127181 | CTGAAAGAAATCTCA[G/T]AGTTTTTAACTATCC | 219333 |
rs150127104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27092616 | GGCAATTCAACAGAG[A/T]AAGAATTGTCTTTTA | 219333 |
rs150128647 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161048 | AACATTATATCCCGT[G/T]TTGTGGAAAAGAGAA | 219333 |
rs150179037 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | USP12 | GRCh38.p7 | 13:27097403 | CCGGGAGGTAGAGGT[C/T]GCAGTGAGCCGAGAT | 219333 |
rs150247855 | snp | A/G/T | 0.0111196 | 0.0737302 | intron-variant | USP12 | GRCh38.p7 | 13:27108817 | ACAAAAATTAGCCGG[A/G/T]TGTGGTGGCACGCAC | 219333 |
rs150257473 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154668 | ACGTGGACGCATTGT[G/T]GTAGTAGAAAAATAA | 219333 |
rs150300406 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27074463 | AGATGAGAAAGCTGT[A/G]ACTTTTTTTATTTGG | 219333 |
rs150335806 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131050 | TGACACTCAAAGTTT[A/C]TGTGTGGCATTTTCA | 219333 |
rs150404725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140021 | AACTGCACTCCCTAC[C/T]TGCAAAATACATTTC | 219333 |
rs150427028 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145752 | AAGTCTGTAACTCTA[C/T]ACCACAAAATTTTGT | 219333 |
rs150534356 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27071453 | TTTGCTTCTATAATA[A/G]AAGACATATTTTTCT | 219333 |
rs150534550 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147304 | CAGGAAAGGAATGCA[C/T]ATCGCCATTTTATTT | 219333 |
rs150605165 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158033 | AGTTTTACTGGGTGA[A/C]CTGTGTTCCCTAATA | 219333 |
rs150648395 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP12 | GRCh38.p7 | 13:27093960 | ATGATTTCAACTACA[C/T]AATATTCTGGAAAAG | 219333 |
rs150652156 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | USP12 | GRCh38.p7 | 13:27069650 | CTATTTTGGACCAAC[-/A]AAATGGTAACTTCTA | 219333 |
rs150692176 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142535 | AAGTTTTTACGAATG[A/T]ACACACAAATATACA | 219333 |
rs150702398 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP12 | GRCh38.p7 | 13:27098951 | TGAAAAACAAACAAC[C/T]GGCTGGAAGCAGTGG | 219333 |
rs150724108 | in-del | -/ATA | 0.0225045 | 0.103662 | intron-variant | USP12 | GRCh38.p7 | 13:27115096 | ATGTTAATTTTATAT[-/ATA]ATAACAAGACACAGA | 219333 |
rs150742294 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | USP12 | GRCh38.p7 | 13:27110281 | AGGTAAATTGTATAA[A/T]CATGTCATTATGTGT | 219333 |
rs150752105 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066348 | CCCAAGGTCACACAG[C/T]TAAATTCACTGAAGA | 219333 |
rs150763692 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124540 | CCAGTTTCATGTTTC[A/G]AGTCATATTTTAGAA | 219333 |
rs150797799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116675 | AGTCAATGACAGGCC[A/G]CAACATGATGGTCCT | 219333 |
rs150811333 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP12 | GRCh38.p7 | 13:27122277 | TCGTGGTAGTGAATA[C/T]GTTTCATGAGAACTG | 219333 |
rs150817470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27089370 | TTAGGGTAAAAAAGC[C/T]TTCTTGGTCTATTCA | 219333 |
rs150860899 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133529 | GCTACCGGTGGGGCT[C/G]AGGTAGGAGAATGGC | 219333 |
rs150867444 | snp | A/C/G | 4.95258e-05 | 0.00497599 | missense, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105868 | GGTTGACTCTTATAC[A/C/G]CAAGAACTTTTTCCC | 219333 |
rs150914003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138079 | GCAGATGTGACCTGA[A/G]CCCTGGCCAGCACAC | 219333 |
rs151007530 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27077282 | AAAACAACAAGGTAT[A/C]CTTTGAGAATTTCCA | 219333 |
rs151059165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151463 | GGTAACTAACAAGAA[A/T]CTTGTATCCAGAATA | 219333 |
rs151069795 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27108300 | AAAAAACCAAACACC[A/G]CATGTTCTTACTCAT | 219333 |
rs151077659 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27086438 | ATGTGTGTATATACA[A/T]ACACACTTTAAAAAT | 219333 |
rs151078900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162358 | TTTGAAAAGGAGTAA[A/T]TTTGTCTCAACCATC | 219333 |
rs151091084 | in-del | -/AGAA | 0.0562307 | 0.157967 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141687 | AATAAATGAATAGAC[-/AGAA]AGGAAGTATTTTTCT | 219333 |
rs151131851 | in-del | -/CAACTC | 0.0970103 | 0.197722 | intron-variant | USP12 | GRCh38.p7 | 13:27089007 | CACAGGAAAACGAGA[-/CAACTC]CAAACTCCAATAAGG | 219333 |
rs151153727 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159601 | TAACTCTCTTTAACA[A/G]TCTGTTCTAGATTTA | 219333 |
rs151225357 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP12 | GRCh38.p7 | 13:27100859 | ACTGCTGAGGACCTA[A/G]TTAAGGTTAGAGATG | 219333 |
rs151268178 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP12 | GRCh38.p7 | 13:27113406 | CCTGTTCTGTGAACA[C/T]GCTAAGATGTTCTAA | 219333 |
rs151279680 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27106187 | ACAAAAACAAAAAAT[-/A]AAAAAAAACAAGATC | 219333 |
rs180868058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27092693 | ACCCAGAATAAACTT[C/T]CTAATACCTTATACA | 219333 |
rs180882641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142596 | AATCACTGGATTTGG[A/G]TAAAAGGTATTTGGG | 219333 |
rs180898080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27102453 | GCTCAGAACCCTCTC[A/G]TGGTTTCCCATGGCT | 219333 |
rs180899604 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27120245 | AAAGTAAACATTCAA[A/T]AATAATAGCTCCATT | 219333 |
rs180910459 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27083079 | ACCTCAGGTGATCTG[A/C]CCACCTTGGCCTCCC | 219333 |
rs180911742 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27073885 | AAATGGTACTGAGAT[C/T]CAAGTTTCTCTCACT | 219333 |
rs180923128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169522 | TTCAAATATGAATAC[A/G]GACACACCCAATTTT | 219333 |
rs180948996 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159198 | AATCAGATATCACAT[A/T]TTTCTTTAAGAGTAT | 219333 |
rs180964898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131264 | GTGTGAAACCCTCCT[A/G]GTGAGAGGGTGAGCA | 219333 |
rs180982712 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153016 | GTCTTTTTTGATTAA[C/T]TGTTTACATTCAACA | 219333 |
rs180993646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27112115 | ACTGTCTAGGTTCAA[G/T]TCTGGTTCCACTATC | 219333 |
rs181106667 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164688 | TTATATGTAAGTTTT[C/T]CAACAATACTGGGAC | 219333 |
rs181117997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127047 | ATCTGGGGGTTCTGC[A/G]CTGATCTGCAGTCAT | 219333 |
rs181128102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149119 | CACCCAGAAGGCAGG[A/G]GTGTGGTAAGACAAG | 219333 |
rs181130191 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27107361 | ACAAATTTATTGATA[C/T]TGTTATTTTGAAACT | 219333 |
rs181136795 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP12 | GRCh38.p7 | 13:27097294 | AACATGGTGAAAGTC[C/T]GTCTCTACTAAATAC | 219333 |
rs181156856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27078490 | TGCATCCATGTTGTA[C/T]TCTAACATAACAGGG | 219333 |
rs181219936 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173262 | GCTCTTTTCTACCCC[C/G]TGTTTGGACAAGGGT | 219333 |
rs181225933 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117300 | AATCTGATAGCACAC[A/T]TCTCTCAGAGCTGAA | 219333 |
rs181246360 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136516 | ATAAACAAATACATA[C/T]ATACATACATACCCT | 219333 |
rs181317889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152235 | AGAAATGGCCCAAAT[G/T]TCCATCAACGAACAA | 219333 |
rs181322401 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168778 | CAACACTAGTGATCT[A/C/G]AAATAAGACACAGCT | 219333 |
rs181326782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130745 | TTCCCCACGACTAAC[A/G]TGGTTTTTTCAGTGA | 219333 |
rs181352428 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27110838 | ATCAATTGAAGAGAA[C/G]ATACAATCTCCATAT | 219333 |
rs181464763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073570 | TGAGTCAGGCATCTC[A/C]GCTCAGTATATTGTG | 219333 |
rs181557675 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106942 | GAAATAAAGAGAAAT[G/T]AATTATTTCAGGTGA | 219333 |
rs181567309 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27087951 | AGAATGAAATATTTA[C/G]AATCTCAAAATGCTT | 219333 |
rs181569114 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067996 | CTGAACACCCTTCCA[A/G]TAAGATTTGTAAAGG | 219333 |
rs181574273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116924 | TTATGTAAGAACGCT[C/T]TGATGTTCGCATGCA | 219333 |
rs181596979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27092164 | AATCTAACAAAACAC[A/G]CATGGTATTGATATG | 219333 |
rs181731149 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125676 | ACCCGGGAAGCGCAA[A/G]GGGTCAAGGGATTTC | 219333 |
rs181748202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27096899 | GAAAAAAATTTAGGG[A/C]AAGTCTAAGATAAAA | 219333 |
rs181766385 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27110075 | GACATGTAATTAAAC[A/G]TGTCCCATTTATGGC | 219333 |
rs181769734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130371 | AAGACAGAAACTTCA[A/G]TGACCACACACAACA | 219333 |
rs181773628 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27091507 | GTCATCAAGTAGGAC[A/G]GTATTCCACTTTTCA | 219333 |
rs181787189 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27072592 | CTGCTTGCCCAAATA[A/C]CCCTTCAGTACAATA | 219333 |
rs181799232 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164341 | TAAATTTTTATTGGT[A/T]CGTAGCTTTGGACAT | 219333 |
rs181867164 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159937 | ATTAAAGCAACTAAC[A/G]TCTGGGATGAAAATG | 219333 |
rs182021660 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27078227 | AATAAGTAAAAAAAA[A/T]TTTTAAAAAGACAAA | 219333 |
rs182027167 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27121030 | AATGGAACGGTATGC[A/C]GGAAACAGATGCTAA | 219333 |
rs182040787 | snp | A/T | 0.00842512 | 0.0643551 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157534 | ATACATGCCTTTTTT[A/T]AAAAAAAATATAAGT | 219333 |
rs182041847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151255 | AGAATCATTTGAACA[C/T]GGGAGGTGGAGGTTG | 219333 |
rs182042743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137709 | CATGCCTTTGTATAA[C/T]TGCCTCCCCTGGAAT | 219333 |
rs182050778 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156356 | AAAATGAAAAAAGCT[A/G]TGTGACAATCTGATT | 219333 |
rs182055607 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140777 | CAGTTTTTCAAATTG[C/T]AAAATATTCATTTGC | 219333 |
rs182062639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163763 | CAATAGAGCAAGACC[C/T]GTCTTAAAAAAAAAA | 219333 |
rs182062908 | snp | C/T | 0.00308231 | 0.0391364 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117836 | TGCACCTGTGGTCCC[C/T]GACGACCATGTGAAA | 219333 |
rs182066895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27100123 | GCCAAGTCATGCATA[A/G]AACCTTGCGTGGTTC | 219333 |
rs182070270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148958 | GGGACACTGAGGGGC[A/G]GATCATTTGAGCTCA | 219333 |
rs182071298 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119264 | ACAAAAAAATAGATA[A/C/T]TCTCCTTAGTTTGGC | 219333 |
rs182075526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27098636 | ATGGCACGTTGTAAA[G/T]GCAATTTTGGTAACA | 219333 |
rs182077970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27078792 | AATCTTTAACAGACT[C/T]CTCTCACTAACAAAA | 219333 |
rs182228181 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067116 | TGAAATTTAACTTGG[C/T]TTTTACGGCATGTTT | 219333 |
rs182260114 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144025 | CCTGGGCAACATGGG[A/G]AAACCCTGTCTCTAC | 219333 |
rs182266167 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27103764 | AAAAAAAAAAAAAAG[A/G]GAGAGAGACAGAGAG | 219333 |
rs182268914 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27122016 | TTCAAAATATAAAAG[C/T]TGGAAAAGCTGAAGT | 219333 |
rs182273386 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP12 | GRCh38.p7 | 13:27084919 | TTTTTCTATTTCTGC[A/G]GAAAATGCCATAGGA | 219333 |
rs182303148 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148224 | AAAGAAAGTTGTTCA[C/G]GCTAGAAGCAAGTGT | 219333 |
rs182312802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167449 | AAACTTCTATTAATA[C/T]TTCTTCTAAATGTTC | 219333 |
rs182317453 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143143 | AAAGTAGTAGTCAGC[G/T]TGGAGGGTTTCCAGT | 219333 |
rs182323472 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | USP12 | GRCh38.p7 | 13:27102784 | TGATGGCTGTCTGCT[C/T]CCCCACGAGGGTGTC | 219333 |
rs182341036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106593 | ATGAGGATAATTCTC[A/T]TATTTCTACTATGGG | 219333 |
rs182373278 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149254 | TCAATCTGACAAAAC[A/G]CATCTATAAAAAACT | 219333 |
rs182468606 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27079513 | GGACTAGGGGAGGAG[C/T]TGGAGGAAGGACTGA | 219333 |
rs182477802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27088381 | GAGATCGCACCACTG[C/T]ACTCCAGCCTGGGCG | 219333 |
rs182490795 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27087407 | CAGCCAACTGTACTG[C/T]CAGAAAAAGGAATTA | 219333 |
rs182579214 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27065737 | TAACAACTCAAGTTA[C/T]TCAATAATGGAACAG | 219333 |
rs182580737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124894 | GCAATGAGAATATTT[A/G]TGACAAAACACATTA | 219333 |
rs182645309 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165716 | TGTCAAAAATTAGCA[A/T]ATAGCTTTGTGAATT | 219333 |
rs182655202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128064 | CCACATAATTCATGG[C/T]TAAATGTGTTATAGA | 219333 |
rs182684803 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27103454 | TATTTCTGAAGTTTA[C/G]AAAAATGAAGCAAAA | 219333 |
rs182686000 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP12 | GRCh38.p7 | 13:27084678 | GTATTCATTCTTAGC[A/C]CCCTTGATGAAGATC | 219333 |
rs182699174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170927 | TTTCAACAGTACTTA[C/T]TTAAAGTTTCCACCT | 219333 |
rs182864188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153571 | AATCGGTACATTAGA[C/G]TTACAGATCCTTTTA | 219333 |
rs182874416 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27118839 | TCTCTACTGTTAGCC[A/G]AATCACATGCCACTC | 219333 |
rs182874543 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170352 | AAAAATATATACAAT[C/G]TACCACCCTTAGATG | 219333 |
rs182877375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133561 | TGAACCTGGGAGGGC[A/G]GAGCTTGCAGTGAGC | 219333 |
rs182998344 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154809 | CCCAGGTGAGCCCTA[C/T]GTAATCACAAGGGTC | 219333 |
rs182999255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156940 | CACTAGACTAAATAC[A/G]GAGAGGTCTCAGGCA | 219333 |
rs183090628 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27108382 | ACTCTGAGGACTGTT[G/T]TGGGGTGGGGGGAGA | 219333 |
rs183093244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156708 | CACCTGTAATCCCAG[C/G]TACTCAGGAGGCTAA | 219333 |
rs183094991 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128400 | CATACTTGAGTGCAC[C/G]ATGAAACTTTACAGA | 219333 |
rs183098036 | snp | C/T | 0.00144839 | 0.0268719 | intron-variant | USP12 | GRCh38.p7 | 13:27089854 | CAAAAAATAAAATCA[C/T]TTAAAAATCCATAAA | 219333 |
rs183108890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139193 | CTTAACAGAGCTTTC[C/T]ATGTATCGATTCATA | 219333 |
rs183113938 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27069686 | GGCACACTGACTCAC[A/G]CCTGTAATCCCAGTA | 219333 |
rs183170666 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27075452 | TGTCCTTGAATTATC[A/C]AACTTTACGATATCC | 219333 |
rs183192038 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27099651 | CCCTAGGAATTTTCC[C/T]TGATATCTCTTGCAT | 219333 |
rs183220605 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068290 | TTATTCCAACAACTA[C/T]AGGAATTTTTAAAAT | 219333 |
rs183270149 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139796 | ATATTTATTTTAAAA[A/G]CATTTTCTTATATGG | 219333 |
rs183274665 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143464 | TAAACATGAAAAAAA[A/C]AACAGAATTAGAAAA | 219333 |
rs183275095 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27114048 | TTCTGAAGGGAAAGC[A/G]CATTTCTTTTTTTGT | 219333 |
rs183294430 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132426 | AAAGCAGTACAGGAA[A/G]GCAAAAAAAAAGAAA | 219333 |
rs183300465 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153148 | ACTAGCCTGGCCAAC[A/G]TGGCGAAACCCTGTC | 219333 |
rs183301737 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27113692 | GCCCTTTTACAGCCC[C/G]TAAAACAGGGCTGGA | 219333 |
rs183321176 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27074061 | GGCAATGGAGGAAGA[A/C]GACGATTATTAAAGA | 219333 |
rs183427281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27121478 | CCAAGAGATTTGAGT[C/T]CATAAGTCAAAAATT | 219333 |
rs183493989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27079718 | GTTCTTTAGATGGAA[A/T]CTGATCCAGAGGACA | 219333 |
rs183501777 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27094483 | CTAAAGCCTGGGCGA[C/T]AGAGCAAGAACCTGT | 219333 |
rs183505594 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160588 | TTTTGTTTTTGGTCC[A/G]TTGTATCTAGTTTTT | 219333 |
rs183534970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099393 | GTCTCGCTATGTTGT[C/G]CAGGCTGATCTTGAA | 219333 |
rs183580145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166296 | TTTAAATCTAAAAAG[A/G]TTTCTGGAAAGGAAT | 219333 |
rs183681807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27079036 | GATATGGAAACTAAG[C/T]AACACATTTCCAAAT | 219333 |
rs183686943 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076343 | CTAAACAATCTTTAT[A/T]ATGCCTTTAAATGCC | 219333 |
rs183731812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149675 | AATACAAAATTACAG[A/C]TCGATAGGAGGAATA | 219333 |
rs183764889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118297 | CCACCAAAACAAGAC[A/G]TTTCTTCTATTATCT | 219333 |
rs183789388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27085426 | CCTCAGGTGATCTGC[C/T]CACCTTGGCCTCCCA | 219333 |
rs183847101 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161615 | CAGGCCAGGTGCAGT[C/G]GTTCACACGTGTAAT | 219333 |
rs183852023 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27122465 | TGGCAGTGTGGAAAC[A/G]GACTAATACACCCCA | 219333 |
rs183897293 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163462 | CTTTTTCCTGAAGCC[C/T]TCTTCTCTCTCCCAA | 219333 |
rs183911730 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27123438 | GTCCTGAATGAGTTA[A/G]GAAATAGCATCATAT | 219333 |
rs183920571 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147293 | AAAACACAACTCAGG[A/G]AAGGAATGCATATCG | 219333 |
rs183920908 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | USP12 | GRCh38.p7 | 13:27106436 | AAATAAACCTACTTT[A/G]TAAAGTAAATGACAC | 219333 |
rs183968804 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27104041 | GCATACTTCTGAACT[C/G]TTTTTTTTTAGAGAC | 219333 |
rs183976605 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066311 | ACAGGGAGACTGAAG[C/T]ACAGAGAGGTTAAGT | 219333 |
rs184027805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145349 | CTAAAACACACCTTA[C/T]CCATTTGGCCAAGAA | 219333 |
rs184044291 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27170110 | CCAAAATCATTTTAA[A/T]ATAGTCCATTTAATA | 219333 |
rs184056467 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27107674 | CTTTTCCCATCCAAA[A/G]GAACTCGGACACCTT | 219333 |
rs184073243 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068920 | ATCTCCTTATCAATA[C/T]GGCACAGATTCCGAT | 219333 |
rs184127389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109539 | ACTTGAAAAAAGGTT[A/G]AAAAGGACTCAAGAG | 219333 |
rs184145279 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167030 | AGGGAATACAACTCA[A/C]GTTTTTTAAAAAGTT | 219333 |
rs184149187 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129123 | AAAGTACTCATATTG[C/T]GAACTATCTAGAAAG | 219333 |
rs184152538 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP12 | GRCh38.p7 | 13:27082799 | GGGGGAAAACGTCAG[C/G]TGGGTGGAGCAGTCA | 219333 |
rs184154003 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27102051 | AATGAATGGACAATA[A/G]GGATTGAAACAACTA | 219333 |
rs184175870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27108666 | TCATAAATTTAAAAT[G/T]ACATTTTAGGCTGGG | 219333 |
rs184204395 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150983 | GGCAAAGGATTGACA[C/T]AGGATTTGGCAAAGG | 219333 |
rs184204897 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP12 | GRCh38.p7 | 13:27089194 | CATTACCGGTACATC[C/G]TGTGATACCAAAATA | 219333 |
rs184220200 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173009 | AAGCACTCAAAAACA[A/G]AAAGCATTCAAACAA | 219333 |
rs184234396 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155591 | TAATTTTCAGAATCC[C/T]GTGCCTAAGAATTTG | 219333 |
rs184259788 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129807 | TTTCAACAACAAGAA[A/G]GCACCACTCTTTGAT | 219333 |
rs184270973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27090538 | GACAGGATATCTGTA[C/T]TGTCATTAAAAAAAA | 219333 |
rs184364149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27105130 | AACTTATTGGCATGT[A/G]AAAATTAAATGAACA | 219333 |
rs184367622 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP12 | GRCh38.p7 | 13:27123041 | AGCTTGCAGTGAGCC[A/G]AGATCGCACCACTGC | 219333 |
rs184375782 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27086308 | ACACACACACACACA[A/C]AATGCAGCACCTCCT | 219333 |
rs184381100 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066565 | CAACATTTCCCTCTT[A/T]CCCTGTTCCCAAGCC | 219333 |
rs184405734 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134249 | ACTAACAACTTATAG[A/G]ACAGAATTTGGAGAA | 219333 |
rs184407617 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067056 | GATGTGAACAAGTAT[A/G]TGATTACCAGGAACT | 219333 |
rs184423403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27095432 | TTGTCAATAAGCAAC[A/G]TTACATTAAGAATAC | 219333 |
rs184438972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130396 | ACAACAAGGAATACA[A/G]ACTTTGCAAAACTGG | 219333 |
rs184445156 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151524 | GGGTGGCTAATGCCT[A/G]TAATCCCAGTGCTTT | 219333 |
rs184448998 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP12 | GRCh38.p7 | 13:27110328 | AAAGGACCTAACCAG[A/G]TAAGTTCATAGGGAA | 219333 |
rs184455102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157698 | ACTTCTCACTTCCTC[A/G]CCAGGACCTTTGTCC | 219333 |
rs184460036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27092000 | CATACGATAACACAC[C/T]GTACTGGAACTGCCT | 219333 |
rs184526464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27087229 | GGTGCACCGACCAAA[C/T]AAGTAAATATAGTGG | 219333 |
rs184528441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27115126 | AGAGACCAGAAGCTT[A/G]TATTTCTACTGATCA | 219333 |
rs184652382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27090319 | TTATCCAAAAGGACA[C/T]TGAATAAATAACCCC | 219333 |
rs184666539 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171463 | CCGCCCGGGCCGCCC[A/G]GGCCGCCCAGCCCGC | 219333 |
rs184670607 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135409 | TTTATATACTCAAAC[A/G]TTTAAGTATTGGGTC | 219333 |
rs184680760 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155328 | CCTCGTGATCTGCCC[A/G]CCTTGGCCTCCCAAG | 219333 |
rs184695290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27116205 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 219333 |
rs184699765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27096441 | ATAATTCCACAAAAC[A/G]TTCCCTGCAGTTACA | 219333 |
rs184702317 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27077198 | AAATTATACATAAAA[G/T]ATAATTCAACTATGA | 219333 |
rs184707333 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158969 | CACACACAATACCTC[A/C]TGTTTGTATATGCAC | 219333 |
rs184728445 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP12 | GRCh38.p7 | 13:27119951 | TTTTCCTTAACAGAA[A/G]TGATCAGGGTACACT | 219333 |
rs184802154 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP12 | GRCh38.p7 | 13:27070454 | CACATGTATAAAAAT[G/T]CATCAAATTCAGATT | 219333 |
rs184844296 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142129 | TCTGTCTCAAAAACA[C/T]ACACACAGACACACA | 219333 |
rs184978893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146431 | ATGTAATAACGCACA[C/T]GGCTAAAGGCTAGGG | 219333 |
rs184981303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116925 | TATGTAAGAACGCTC[C/T]GATGTTCGCATGCAC | 219333 |
rs184988223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27078396 | CATGCATTTTGCTCT[A/T]TGTGAGGGTCCTGGA | 219333 |
rs185090739 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27097001 | CTTTAAAAAAGTTTT[A/T]AAAAAAGTGAAACCT | 219333 |
rs185116373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27083119 | GGATTACAGGTGTGA[A/G]TCACTGCACCTGGCT | 219333 |
rs185169863 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161943 | TGTACATTTTTAACA[C/T]AGTAAAGATTTTAAG | 219333 |
rs185182301 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159200 | TCAGATATCACATTT[G/T]TCTTTAAGAGTATAT | 219333 |
rs185182911 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135829 | GCCAGAAGCTAGCTA[A/G]GGAGGGGAGAAGGCA | 219333 |
rs185201736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142715 | CAAAATCGAGACTAA[C/T]TTGAACATCACCAAA | 219333 |
rs185204010 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | USP12 | GRCh38.p7 | 13:27073972 | TTCACTCCTTTAAGA[A/T]GTGATCACTCTTAAT | 219333 |
rs185205640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27102485 | TCCAAATAAAACCCA[A/G]GCTTTAGGCCCCTGT | 219333 |
rs185211480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27120319 | TTTATGAAATCAGTG[A/G]TTCTTTACTGGGATA | 219333 |
rs185221875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27101578 | GACAGTCTAGTGGGA[A/G]AGACAGACAATTTCA | 219333 |
rs185253093 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165334 | AAATTAGTGCTTTCT[C/G]AGGGGTATATACTAC | 219333 |
rs185258885 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127955 | TAACTTTCAAAAGTT[C/T]AAACGTCCACTAGAA | 219333 |
rs185266165 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149197 | TAACAAAAGAAAAGA[C/T]TGATTTACGGAATTA | 219333 |
rs185272881 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168124 | TCTCCTAGCACCTAC[A/C]TTTACCAGCTTTGGC | 219333 |
rs185311975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141651 | CACATGAACAAAACA[A/G]AAGTCCATGCTACTC | 219333 |
rs185349413 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27081628 | CCAGAATGGTGAATC[A/C]TTTCCAGAGGGGTTT | 219333 |
rs185430082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27119677 | CTTCTGAAGACATTA[C/T]TGTTTTAACACAAAA | 219333 |
rs185454237 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27078569 | AAGAAAGAAGGATGG[A/G]AAAAGACATACCATG | 219333 |
rs185493282 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152279 | AGTATATCCACACAA[C/T]GGAACAATATTTGTC | 219333 |
rs185507315 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27169111 | GATCAAACTGCAGAA[A/G]TAAATGATAATCCTT | 219333 |
rs185507700 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP12 | GRCh38.p7 | 13:27121517 | ACACAGGAAAAGAAA[A/G]CCCCATGAATAAGAG | 219333 |
rs185508631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125523 | ACAGCTCCGGTCTAC[A/G]GCTCCCTGCGAGATC | 219333 |
rs185512767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130892 | AATTCTTGAAGGCAA[C/T]AACATTTAAATTCCA | 219333 |
rs185515075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27103474 | ATGAAGCAAAACTTA[C/T]GAGAAGATGGGCTTA | 219333 |
rs185519854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27084711 | TTGCCTGTATATGTA[C/T]GGTTTTATTTCTGGG | 219333 |
rs185603817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163985 | GAGTTTATCACAGTC[A/G]TCTTCATGTTCTCAG | 219333 |
rs185674972 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068041 | GGAAGGACTTGTCTT[C/T]TGTATTCCCGGTCTA | 219333 |
rs185725224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148287 | ACATACAAGAGTACC[C/T]GTAACAGCAATTGTT | 219333 |
rs185738527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149065 | GGCACACGCCTGTAG[C/T]CCCACCTACTCAGGG | 219333 |
rs185748433 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27107267 | GAGGCGGAGGCTGCA[A/G]TGAGCCAAGATCGCA | 219333 |
rs185750486 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125900 | CTGGAGCTTGGCAGG[A/G]GGAGGGGCGTCCGCC | 219333 |
rs185767498 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP12 | GRCh38.p7 | 13:27088187 | GCTCTCTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 219333 |
rs185814332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153019 | TTTTTTGATTAATTG[C/T]TTACATTCAACATTT | 219333 |
rs185821250 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | USP12 | GRCh38.p7 | 13:27112545 | CTCTCGTCTTGGCCT[A/C]CCAAAGTGCTGGGAT | 219333 |
rs185955076 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131711 | TTTTATTTTATAAGT[A/C]CTCTAAGTTCACAAT | 219333 |
rs185971063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27093208 | AAAAACTTCCACTCT[A/G]CCAAAAACAGTGTTA | 219333 |
rs186024907 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP12 | GRCh38.p7 | 13:27169778 | ACTGTTTGTGTCCAT[A/G]AGCAAGAATGTAAAC | 219333 |
rs186066548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27107530 | TATCAACATAAACTT[A/G]TAACTCTGAAAATGT | 219333 |
rs186072262 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068680 | GCCACTTTTGACCAA[C/T]TGCTCCCTACATATA | 219333 |
rs186112351 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129165 | CTTACCACAATAAGA[A/G]AGTGACCTGTAGCTC | 219333 |
rs186146035 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173451 | CCTCCATCCCGCTAA[C/T]CACCCATATGCCTCC | 219333 |
rs186191845 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156194 | TAAGTTTTTCCACCA[C/T]CACTTGTACCTCAAC | 219333 |
rs186199948 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117569 | AGTATCTCAAAAACA[C/T]AATGTTAAATGAAAA | 219333 |
rs186201393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27088606 | AGTCTGGAATTTGGG[A/G]GCATGGTAGGCAGAG | 219333 |
rs186259574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27170150 | TCCTAAAATGTAAAC[C/T]GTGAGAAAGAACAAT | 219333 |
rs186312181 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27092370 | TCGACGAACTTGATT[A/C]TAAAGTTTACATGGA | 219333 |
rs186350144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160748 | TGATTCCTATTCCTC[A/G]CCTGTTCTTAAAAGA | 219333 |
rs186407852 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27078916 | CTTCTCAAGTTCAAC[C/T]GAAACATTCACTAAT | 219333 |
rs186451072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156438 | GATATAGTGACGAAA[C/T]GCAACGATGATCATT | 219333 |
rs186457138 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137877 | AAGGAGCAAGCTGCC[A/G]CGCTGAGAGGACTTA | 219333 |
rs186474003 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118078 | GTGAAGAGCTGCAGA[G/T]ACAACATGCCTCTTC | 219333 |
rs186486841 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27110871 | TGGAATAGGCAACAG[A/G]GGAATTGAACAACTT | 219333 |
rs186511816 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27073579 | CATCTCAGCTCAGTA[C/T]ATTGTGAGTAGAGCA | 219333 |
rs186520474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27103865 | TGACAAACAAACATA[C/T]AAAGCCATAAGTATG | 219333 |
rs186523920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27076509 | TTCACTTTATATATG[C/T]CAAGCTTATTACATG | 219333 |
rs186572316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143838 | AGAGCAAATTAAAAG[A/G]CACCATAAGGAAATG | 219333 |
rs186594570 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27118675 | ATAATCCTTTCCCCC[A/G]ACCAAAACAGAAGAA | 219333 |
rs186601433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160860 | GTGACACAGGTAAAC[A/G]TATCATGGTGGTTTG | 219333 |
rs186608445 | snp | C/T | 0.00184218 | 0.0302935 | intron-variant | USP12 | GRCh38.p7 | 13:27095579 | CAATTTTTCTCTATA[C/T]AAAATTGTATGATAT | 219333 |
rs186610041 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27122231 | GGTAAGAAATAATTT[C/G]AATCATCAGGGTGGT | 219333 |
rs186614196 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144080 | GTGGTGGCACATGCC[A/T]ATAGTCCCAGCCTCT | 219333 |
rs186695390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156801 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGATTCC | 219333 |
rs186808883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27118873 | TTGTATTCTAACCAC[C/T]CCACATGTCCACCTG | 219333 |
rs186823955 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP12 | GRCh38.p7 | 13:27079545 | ATTGCCTGCAACCAC[C/G]CTCAACCGGAATACC | 219333 |
rs186825479 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27100099 | TCCACTCCATCCCTC[C/T]GAGGCCGGGCCAAGT | 219333 |
rs186830144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164452 | CCTTCTGAAAGAGAA[A/G]CAGCAGCAAAGCATA | 219333 |
rs186832796 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139570 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 219333 |
rs186846755 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP12 | GRCh38.p7 | 13:27099410 | AGGCTGATCTTGAAC[C/T]CCTAGGCTCAAGCAA | 219333 |
rs186881422 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143344 | TCCTTATTCTGAAAA[C/G]TGGCAACTAAAGACT | 219333 |
rs186901284 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | USP12 | GRCh38.p7 | 13:27102785 | GATGGCTGTCTGCTT[C/T]CCCACGAGGGTGTCA | 219333 |
rs187020072 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150791 | CAACAAGAGTGCCAA[A/C]TCCAAAAGACAGAGA | 219333 |
rs187027619 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167132 | CTGGGCGTGGTGGCA[A/C]ATGCCTGTAATCCCA | 219333 |
rs187072985 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27121173 | CAAGAAACAGCAAGA[C/T]AACTTGCTTGACTTG | 219333 |
rs187104781 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27084066 | GACAGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 219333 |
rs187157610 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP12 | GRCh38.p7 | 13:27087594 | GCGGGCTCAGGAACA[A/G]TGACATCCCAATAGC | 219333 |
rs187166119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160028 | GAACACTTGGCAGGA[C/G]GAGTAACCTGAGCAA | 219333 |
rs187234997 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162409 | TGTAGATGTCATAAC[A/G]AGTTTGCATGTCTAG | 219333 |
rs187242995 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170423 | AAATAGGGCCAGTGA[A/G]GCATGAAACACAAGA | 219333 |
rs187248562 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146852 | GCTAATCAAGTTAAA[A/T]TGAGGTCATGAAGGT | 219333 |
rs187373635 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067249 | TAATGTTAAAACTGA[C/T]ACAGCTTCACTTTCC | 219333 |
rs187394329 | snp | C/T | 1.70223e-05 | 0.00291734 | intron-variant | USP12 | GRCh38.p7 | 13:27089880 | ATAAAGCTCTAAAAT[C/T]ACCGTTTGTGTGCTT | 219333 |
rs187403821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27069764 | ACCAGCCTGACCAAC[A/G]TGGAGAAACCCCATC | 219333 |
rs187450417 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166338 | TACAAATGCTTAAAA[A/G]ATACTTCCTGAGACA | 219333 |
rs187459302 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128812 | ATGCTTTTCCACTTA[C/T]AAAAACATGAACGCT | 219333 |
rs187461969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150136 | AATGTTTGAAGTGAT[A/G]GATATGCTAATTCCC | 219333 |
rs187468453 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27108574 | CAAGATTAGCCTGGG[A/G]TATCTTAAATATAAG | 219333 |
rs187487726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27084995 | ATGGACATTTTAACA[A/G]TATTAAGTCTTCCAT | 219333 |
rs187535531 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155105 | TTTTTTTTTTGAGAC[A/G]GAACCTCGCTCTGTC | 219333 |
rs187605088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27093760 | ATAATTGGCAAAACT[C/T]GGAAGCAACCAAGAC | 219333 |
rs187606691 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP12 | GRCh38.p7 | 13:27074260 | AAAAAATTAGCCGGG[C/T]GTGGTGGTGGGTGCC | 219333 |
rs187669367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132685 | TCTATGTGTGTGAGG[A/G]GCTGGTGGGCACGTT | 219333 |
rs187672122 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153482 | AAATCTAGTAACAAT[A/T]AACTCCAAAAATGGG | 219333 |
rs187682569 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27113739 | GGCAGAGGACCTGGG[C/T]CAGAGCTCTTTTCCC | 219333 |
rs187749529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139833 | TGTGCCAGGAACTAT[A/G]CTAAGGACAGGTGAT | 219333 |
rs187751662 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27065896 | CTCTAAGATTCTATG[A/G]CTCTCAATGTTCAAA | 219333 |
rs187755815 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27109388 | ACTTTAATCAAGTCT[C/G]TACGTGTAACTACTA | 219333 |
rs187760137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27100566 | ACTTTGCCTCCTGCA[C/T]CAACCTTGACATGTC | 219333 |
rs187762221 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27119424 | TGGAAAGAGCTGTAG[A/T]TCATCATCGTTTAAC | 219333 |
rs187773743 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171042 | TCTCCCAGGCGGGAA[G/T]GAGCGCTGCCCGCCC | 219333 |
rs187802109 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134896 | TGAATTTTAAAGTGC[C/T]GTAAACAGACGTACA | 219333 |
rs187834541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157691 | TTAATTCACTTCTCA[A/C]TTCCTCGCCAGGACC | 219333 |
rs187852828 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141311 | TGAGCCACCATGTCC[A/G]GCTGTGAAGTCACTT | 219333 |
rs187933953 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069139 | GCTTGTCAATCCATC[A/G]TCTTTGCTTTATCGT | 219333 |
rs187989630 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133750 | CTATTTCACTAATAA[A/T]CACCAACAGTTTTCT | 219333 |
rs188002041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27094568 | AAATTAATTTCACCA[A/G]TGAGAGGCAGATGGA | 219333 |
rs188018117 | snp | A/C | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129460 | CAGGTGCAGTGGTTC[A/C]TGCCCATAATACCAG | 219333 |
rs188034505 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27090342 | ATAACCCCTACCAGA[G/T]GTATAAATAAAACAC | 219333 |
rs188038363 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157279 | GATAAGTTTTACATA[C/T]ATTAAGCTAAAAAAC | 219333 |
rs188193122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124379 | CTATTTTATAAAGTA[C/G]AGAACAATACACCTT | 219333 |
rs188199181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148179 | CAGAAGTTGTTCCTA[C/T]GCTAACAGACATACC | 219333 |
rs188253629 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP12 | GRCh38.p7 | 13:27079222 | CCCTGTGTGGGGCGG[C/G]GGGGAGTGGGGGGAG | 219333 |
rs188266899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137149 | TGCCAGTAGTCTTCC[A/C]TATTACAAAATATAT | 219333 |
rs188275658 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117640 | GTGTTTAATAGCACA[C/T]GGAAAGCAGACCGAA | 219333 |
rs188282070 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27114062 | CACATTTCTTTTTTT[G/T]TTATTTTTAAAACAA | 219333 |
rs188282886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163479 | CTTCTCTCTCCCAAA[A/C]CCACCTTCTCTTTCA | 219333 |
rs188290627 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27075484 | ATGAACAGATAGACA[A/G]TGGTCAGTTTTAATA | 219333 |
rs188353329 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154256 | CTTAACATCCTAAAA[C/T]ATATTTTACATATAC | 219333 |
rs188437036 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | USP12 | GRCh38.p7 | 13:27102424 | TCAAACAAATCAGAA[A/C]GTATCACCCACCTGC | 219333 |
rs188440991 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27082984 | GGGATTATAGGCATG[A/C/T]GCCACCACGTCCAGC | 219333 |
rs188506894 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142497 | TGAAAGAGAATGTCC[C/G]TGTTACTGGGAAATG | 219333 |
rs188526649 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145723 | TTGTCCTAAAGTCCC[C/T]TCTTTATCAACAAAA | 219333 |
rs188529431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119994 | CTAACGCTAACTAAA[A/G]AGGCAAAAGATTATA | 219333 |
rs188559797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104231 | AGACAAGGTCTTGCT[C/T]TGCTGCTGAGGCTAG | 219333 |
rs188576803 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066402 | TCCCAGCTCCCAGCC[A/G]AATACCTCATGATAG | 219333 |
rs188688780 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27086761 | ATTTAGTCCCTGACT[A/C]TTACTTATCCAACGG | 219333 |
rs188690851 | snp | G/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066657 | CTTAAGAAGTGGGAC[G/T]TAATTTAGAATATTT | 219333 |
rs188766348 | snp | A/T | 3.29658e-05 | 0.00405978 | synonymous-codon, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105771 | GAACTTCTTAGGGGG[A/T]ATTACTCCAACCTTT | 219333 |
rs188770138 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | USP12 | GRCh38.p7 | 13:27123317 | GTCTATAGTACCTTC[C/G]ATCCCCACATTTTTA | 219333 |
rs188799062 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128231 | CAATGAGACAATGAG[A/C]TAATGAAAGAAATCT | 219333 |
rs188809062 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27089429 | CAAAATAAGAAGTAA[C/T]GATGATGATGATGTT | 219333 |
rs188819409 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161623 | GTGCAGTGGTTCACA[C/T]GTGTAATTGCAGCAT | 219333 |
rs188821501 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27122600 | GAAGCTGCAGTGAGC[C/T]GGGAGTGTGCCACTA | 219333 |
rs188839718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27085541 | CTCAACACAAGCTTA[C/T]CCTATTATTCCAAGA | 219333 |
rs188843089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27110803 | ATCTAATCAAGCTAA[C/T]GACCAACAAATCTGG | 219333 |
rs188856517 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27092029 | CTGAACACTGCTTTG[C/G]CAGTCTTCATTACCA | 219333 |
rs188863156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073554 | GGGGACCCCTCCCCA[A/G]TGAGTCAGGCATCTC | 219333 |
rs188865501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165733 | TAGCTTTGTGAATTA[A/T]TAGGCTGTTGGTGAC | 219333 |
rs188918597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168438 | CATGACGGACCACCC[A/G]GATTAGCCACCTCAA | 219333 |
rs188929482 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130587 | AAAAAGGAAAATATG[G/T]TGTATTTGCAGGAAA | 219333 |
rs189061784 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149306 | TAGCGAAAACACTGG[A/C]TGCTTTTCCTCTAAG | 219333 |
rs189078496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27080709 | AAGTTCAGTTCCAGG[C/G]CACCGCAATAAAGTG | 219333 |
rs189085681 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067703 | TTGTTTTCCATAGTC[A/G]ACAGTTTTAGCAAAA | 219333 |
rs189086604 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27107677 | TTCCCATCCAAAAGA[A/T]CTCGGACACCTTGAA | 219333 |
rs189093218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116778 | CTTACGTTTAGATAT[A/G]TTCAGATGCACACTT | 219333 |
rs189100960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27087299 | CGCGCACGCTCGTGT[A/G]CATGCAGGGAGCGGG | 219333 |
rs189101479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27096529 | TGTGCTTGGCAATAT[A/G]CAACTCTACCATAGA | 219333 |
rs189107422 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27077727 | TGAACATACGTGTAA[A/G]GAGTCTGAAACTCAT | 219333 |
rs189159636 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155354 | CCAAGGTGCTGGGAT[A/C/T]ACAGGTGTGAGCCAC | 219333 |
rs189168139 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171465 | GCCCGGGCCGCCCGG[C/G]CCGCCCAGCCCGCCC | 219333 |
rs189171644 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135418 | TCAAACGTTTAAGTA[C/T]TGGGTCTATGGAGGC | 219333 |
rs189325565 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27072505 | ATTAAACACACTCAG[C/T]TGAGTAGATACAAAT | 219333 |
rs189360582 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27071404 | TACAGCTATATTACT[C/G]AAATTTTTTACTGTC | 219333 |
rs189381148 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27106560 | ATTTGGGGAGCACTA[C/T]GAAACTATAAAAAAG | 219333 |
rs189387598 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067074 | ATTACCAGGAACTCA[A/C]CACATACACTAGAAC | 219333 |
rs189421606 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27091255 | TGGCAGAGGTAGGCT[A/G]GCCAGATCAGGCCGG | 219333 |
rs189424883 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173887 | GGCACAGTGGATCAG[A/G]CCTGTAATCCCAGCA | 219333 |
rs189520099 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27120911 | CTGCAGAAATCAAAA[A/G]ACAAAAGTGATGGGG | 219333 |
rs189526696 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142788 | TAAATAAAAATCTAT[C/T]GTGACACAAAAAAGA | 219333 |
rs189605481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159650 | AAACTCAAACTTTCC[C/T]ACACCTTTATTTTTT | 219333 |
rs189652501 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136462 | AAGATCATGCCACTG[C/T]ACTCCAGTCTGGGCA | 219333 |
rs189668839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27097034 | AAATTATTAACATTT[G/T]CAACATATAAAAGCA | 219333 |
rs189669353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159120 | TTTTAAAAATAGTAA[A/G]TGGTTTGGTTTTTCT | 219333 |
rs189676725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165557 | CCAGGTACTAGTCAA[C/T]AACCCTATGAACTAG | 219333 |
rs189732153 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173096 | TTATAAGCTTGCTTG[G/T]GGGGGGAATGCAGAT | 219333 |
rs189751611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27097815 | TACATGTTGAATATC[C/T]TTTATCTAAAATGCT | 219333 |
rs189754089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27078615 | AGTAAACTGGCTATA[C/T]TAATGTCAGACAAAG | 219333 |
rs189897259 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158163 | GTGGACCCTAATCCA[C/G]TGTGACTGGTGTCTG | 219333 |
rs189898792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155941 | TATAACATAGATGTA[C/G]ATTCTCTTTCAATGT | 219333 |
rs189903478 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27119735 | TATGCCAAGCCCACA[A/G]TTCAACAGCTTGAAG | 219333 |
rs189912498 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116938 | TCTGATGTTCGCATG[C/T]ACAATGACGAAATGG | 219333 |
rs189917902 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27121593 | TAAGGCAGGCGTGGT[G/T]GCTCATGCTTGTAAT | 219333 |
rs189922017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169174 | TCAAAGAAAAATTTA[C/T]TGCACAGTAAGTATG | 219333 |
rs189929540 | snp | C/T | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27081774 | AGAATGGATCTTATG[C/T]TAGCAGGCATGAAAA | 219333 |
rs189932779 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP12 | GRCh38.p7 | 13:27078424 | GGAACCAACTGATAC[A/G]GAGCATAACTGTATG | 219333 |
rs189934482 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27084719 | ATATGTATGGTTTTA[C/T]TTCTGGGTCATTTTG | 219333 |
rs189985570 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160762 | CACCTGTTCTTAAAA[A/G]AACCAAAGCATCATG | 219333 |
rs190005939 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144006 | GTCAGGAGTTCGAGA[A/C]CAGCCTGGGCAACAT | 219333 |
rs190156955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27107295 | GCACCACTGCACTCC[A/G]GCTTGGATGACAAAG | 219333 |
rs190163549 | snp | A/C/T | 0.00438476 | 0.0466401 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141982 | TAGTTGGGCGTGGTA[A/C/T]ATGATGGCGTGTGCC | 219333 |
rs190167057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27088193 | TGGGAGGCCGAGGCA[A/G]GCGGATCACGATGTC | 219333 |
rs190178148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27101881 | TTAAATTTATCTGTT[G/T]TTGTATCTCTCCACG | 219333 |
rs190181646 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068243 | TAAGAATTCTAAAGA[C/T]TGGTATACCACCACT | 219333 |
rs190205374 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148858 | TGTCATGATAAAAAC[A/C]TAGAAAAGAATTCCT | 219333 |
rs190232152 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27106795 | AGAGATGGATAAAAA[C/T]GAGACTTCTCTGAAA | 219333 |
rs190233922 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164650 | AAGCAAATTCTGCAC[A/G]TAAGATAGCAAATGG | 219333 |
rs190245732 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126901 | CAATGCCTGGCACAA[A/C]AGGCACAAAGCAAAC | 219333 |
rs190247899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149096 | GACTGAAATGGAAGA[A/G]TCACTTTCACCCAGA | 219333 |
rs190435620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164318 | TACTTCTTGTTTTCA[G/T]TTGGAAATAAATTTT | 219333 |
rs190440439 | snp | A/T | 0.11133 | 0.208016 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167274 | TCTCAAAAAAAAAAT[A/T]AAATAAATAAATAAA | 219333 |
rs190451827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27102507 | GGCCCCTGTTCTTCT[A/G]ACTTTATCTTCATCT | 219333 |
rs190469925 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125665 | GGCGTCCCCTCACCC[A/G]GGAAGCGCAAGGGGT | 219333 |
rs190470097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130267 | CCCCTTAGGCTGCAA[C/T]CTTTCTTGTTTTTTT | 219333 |
rs190482314 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27087689 | GAGAAATGGCTTGTT[A/C]CAGAGTAGGGGCAAA | 219333 |
rs190587320 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132941 | GCTATTCTGAATGAA[C/G]TTCTTTAATTACCAT | 219333 |
rs190608975 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | USP12 | GRCh38.p7 | 13:27113902 | ATGAACTTTATAACC[A/C]AAAAATGGAAAGTTT | 219333 |
rs190616584 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27094082 | CAGTAAAGATGAGAT[C/T]AGGCAAAATCATAAA | 219333 |
rs190677321 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153564 | ATCCATTAATCGGTA[C/T]ATTAGAGTTACAGAT | 219333 |
rs190685264 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27170183 | TCCAGTTGGGAAATG[C/G]AGTCTTCAATGATTC | 219333 |
rs190708186 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150985 | CAAAGGATTGACACA[A/G]GATTTGGCAAAGGAT | 219333 |
rs190714428 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP12 | GRCh38.p7 | 13:27083536 | CAGGGCGATCACTCT[C/T]CTCTCACCTATATGC | 219333 |
rs190716683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109757 | CGTCTCTACTAAAAA[C/T]ACAAAAACTAGCCGG | 219333 |
rs190747714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128000 | TTAGACATGTCAAAA[A/G]GCACAGTATTCCGAT | 219333 |
rs190774546 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27088715 | TGTGGGAAGAATTAA[C/T]AGTCTTTTGTGACTC | 219333 |
rs190845265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139114 | ACTTTTCCCAGATTT[A/G]TGATTTCTTTGGGAA | 219333 |
rs190847183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27089701 | GGGTACACAGTTTTT[A/G]TAAAATAAACATTGA | 219333 |
rs190855500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27098864 | ATGGAAACAGTTCCA[C/T]TGAATTAACATGGCA | 219333 |
rs190855789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118285 | GGCAGTCAAGTTCCA[C/T]CAAAACAAGACGTTT | 219333 |
rs190922438 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156443 | AGTGACGAAACGCAA[C/T]GATGATCATTATGGA | 219333 |
rs190927454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27107681 | CATCCAAAAGAACTC[A/G]GACACCTTGAAGATA | 219333 |
rs190983276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152487 | GGAGGGAAAGGAAAG[A/G]AGGAGGAGAAAAAGA | 219333 |
rs190984800 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149206 | AAAAGATTGATTTAC[A/G]GAATTAATAAAATAA | 219333 |
rs190996210 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161561 | AAAAAATGTTACTAA[C/T]AGGGAATTGCAGTGT | 219333 |
rs191013326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27111586 | GAGCTTTCTCTAATG[C/T]CTTCTTCTCCAAACC | 219333 |
rs191014320 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27107672 | CCCTTTTCCCATCCA[A/G]AAGAACTCGGACACC | 219333 |
rs191027495 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068690 | ACCAATTGCTCCCTA[C/T]ATATACATATACTGT | 219333 |
rs191028021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073851 | CTATGCATAACGTTA[C/T]ACTGCCCACAATTGG | 219333 |
rs191084168 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27093324 | GAAAAAAAAAACCCA[C/T]TTAAAATTCGACAAT | 219333 |
rs191102230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074028 | TGAGGATAAAAGACG[A/G]GACCCAAGGCTGACC | 219333 |
rs191173981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113662 | ATGCAAATTACTGTC[A/G]TGTTATCAATCAAAG | 219333 |
rs191243677 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | USP12 | GRCh38.p7 | 13:27118928 | ATGCCTGCTTAGTAA[C/G]CTCTTCTCCCACTCC | 219333 |
rs191249527 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131104 | AAAATAAGCACAGAT[G/T]TACATATGTTAAACA | 219333 |
rs191251811 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27079698 | TATAAATTGTGTGAG[C/T]CAGAGTTCTTTAGAT | 219333 |
rs191259097 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27092469 | GACTTTAAGACTTAC[G/T]CTAAAGCTACGGTAA | 219333 |
rs191306019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157377 | GTGTACATAATTCCC[C/T]GTCATTACTTTGGGA | 219333 |
rs191317461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139733 | TACAAATAAATGCAG[G/T]TGAAGTCACATACAA | 219333 |
rs191318512 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140722 | TCATATATAAAGCAA[A/T]TTTAGATATAATAAA | 219333 |
rs191321657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27099536 | CCATTTAAATCTACC[C/T]AGTTCAAGTCACCTC | 219333 |
rs191473905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27079304 | TGGCTTCAGCTCAGT[C/G]TCAGAGAACCCCAGA | 219333 |
rs191542228 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156836 | CAAAAAAACAAAAGA[C/G]AGAGAGAGAAAAAAT | 219333 |
rs191552404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27118736 | ATACTTACCCATCTA[C/G]AACAATAAAATACCA | 219333 |
rs191554171 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160468 | AAATGAAACTAACCA[C/G]TAAACTTTAAAAAAG | 219333 |
rs191557487 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27121453 | CACGAAGAATTCCTA[A/C]AAATACAAGCCAAGA | 219333 |
rs191574493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27084603 | AACTTTATTCTTTTT[C/T]GTGTGGATATTCAGT | 219333 |
rs191659313 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146996 | GGAATGCCTGAGGCT[A/G]CCGGAAGCAAGTAGA | 219333 |
rs191665305 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP12 | GRCh38.p7 | 13:27106159 | GGTTCTTAGGTACAT[C/G]CAAATTAAAACACAC | 219333 |
rs191668611 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27123388 | CATTAAATATACAAT[A/G]TTGGATAGTCTATTA | 219333 |
rs191672810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27086910 | AATCTGTTTTGATTC[C/T]GTGGTCCATTACCAA | 219333 |
rs191685867 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066797 | ACTTACACCAGCCCC[A/G]CATTTTAATCACAGT | 219333 |
rs191728933 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162943 | GTATTTATCCTTAAT[G/T]TTTTAACATGTATAT | 219333 |
rs191804743 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143366 | CTAAAGACTTCATTA[C/T]CTACTTTGTCTTTTC | 219333 |
rs191823318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27078980 | AAAGATGAAATCAGA[C/G]TATGTCCTCTGATAA | 219333 |
rs191827866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074816 | TTTCCAATGCCATTT[A/T]AAAATGCTTTTTACA | 219333 |
rs191847937 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27103290 | GAATAATATATTAAA[A/T]CCTCTTTGATTTGTA | 219333 |
rs191859870 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149564 | ACATAGCCATCAATT[A/G]TATTGATCTCATAAA | 219333 |
rs191866357 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129103 | CCATACACTTCAAAT[A/T]AAAAAAAGTACTCAT | 219333 |
rs191871775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150297 | GAAAATGAAAATAAG[A/G]CAACTCCATTCACAG | 219333 |
rs191872111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27108642 | AAAACACACCAACTA[C/T]ACAAAAATTCATAAA | 219333 |
rs191875272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27081866 | AAGCAGTAATATTTT[G/T]AAAGAAATCTTTGTT | 219333 |
rs191885307 | snp | A/G | 1.65883e-05 | 0.00287991 | missense | USP12 | GRCh38.p7 | 13:27089908 | CTTCCTGTTTGCTGC[A/G]ACACTCTTCACAGTA | 219333 |
rs191889677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27070430 | CCATGTGTGTGTGAC[A/G]TGGGGGGACACATGT | 219333 |
rs191949015 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166684 | GAATATGGTATTTAA[A/G]ACTAGAGTTTTCAAG | 219333 |
rs192055842 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27169808 | CACCAAGAAAACAGG[A/G]GCTGCCCTGACCAAT | 219333 |
rs192084320 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132109 | GGAAATAAGCACATT[C/G]ACCTTTCCTGCTATC | 219333 |
rs192096597 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155361 | GCTGGGATCACAGGT[A/G]TGAGCCACTGCACCC | 219333 |
rs192107917 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172681 | CAGGAAGCCCGCAAG[C/T]AAGAAAAATGCCCTG | 219333 |
rs192116843 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27086020 | AATAAAATTCAATAA[A/T]TTATTCAGGCACGGT | 219333 |
rs192118217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135472 | AATCCCAGCACTTTC[A/G]GAGGCCGAGGCAGAT | 219333 |
rs192129227 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066560 | TAATACAACATTTCC[C/T]TCTTTCCCTGTTCCC | 219333 |
rs192152279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165986 | TGATACCAATAATCA[C/T]TTATAAACTACTAAA | 219333 |
rs192181012 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128335 | CACATTTGGCTTAAC[A/C]ATAACATCAAAAGGA | 219333 |
rs192345492 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167202 | GGGAGGTGGAGGTTG[C/T]GGTGAGCCAAGATTG | 219333 |
rs192350507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157697 | CACTTCTCACTTCCT[C/T]GCCAGGACCTTTGTC | 219333 |
rs192357646 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129786 | CCATTAATGTAGTTT[C/T]GGTCTTTTCAACAAC | 219333 |
rs192358237 | snp | A/T | 1.65173e-05 | 0.00287374 | intron-variant | USP12 | GRCh38.p7 | 13:27069408 | TAAAATGTAAACATT[A/T]GTACATAAATGAGCT | 219333 |
rs192368262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27090346 | CCCCTACCAGATGTA[C/T]AAATAAAACACCAAA | 219333 |
rs192371639 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141551 | AAGAATGATAAAAAC[A/C]TGACAAACAAACACA | 219333 |
rs192436488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153065 | GGCCGGGCATGGTGG[C/T]TCACACCTGTAATCC | 219333 |
rs192524336 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP12 | GRCh38.p7 | 13:27075794 | CAACACTTTGGGAGG[C/T]CGAGGCAGGTGGATC | 219333 |
rs192587261 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154266 | TAAAATATATTTTAC[A/G]TATACTCTGTTGAGC | 219333 |
rs192601183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27114184 | CTACCTGTATTAGAA[A/G]ATTAATAAAGAACCA | 219333 |
rs192605701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27116030 | AAGATGTCAGGCAAC[C/T]GGCTGGGTGTGGTGG | 219333 |
rs192621246 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27096075 | AGGGCAAAACCTATC[C/T]TTATATATTGGCATA | 219333 |
rs192626046 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076719 | TTTAAAGAAGTGATA[C/T]ATGGTAAGCCACTGC | 219333 |
rs192687945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27071680 | TAAAAGCAAATGACC[C/T]TTGCTCAATGGTAAG | 219333 |
rs192695409 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135159 | TGGCATGGTGGAGTG[C/T]GTCTGTAGTCCCAGC | 219333 |
rs192719916 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150893 | ACCTCAAACCATGTA[C/T]AAAAAACTAACTCCA | 219333 |
rs192738854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109431 | GTCAACAGTCAGGCA[A/G]TGAAAGAGACAATAC | 219333 |
rs192759695 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101968 | CTCATCCCTAGGACT[G/T]ACAACCGTGCCTGCC | 219333 |
rs192793586 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142001 | ATGGCGTGTGCCTGC[A/C]GTCCCAGCCACTTGC | 219333 |
rs192840754 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170857 | AAGACTGCCACCTGG[A/G]CACACGGCTGGAAAC | 219333 |
rs192856955 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133958 | GCAACACAGTGAAAT[A/C]CCATCTCTAAATAAA | 219333 |
rs192862713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27094593 | GATGGATATTGTGTG[C/T]CTACAGACGTGATGC | 219333 |
rs192920767 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161833 | GTTTCAATGAGGCGA[G/T]ACTGCACCACTGCAC | 219333 |
rs192926768 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP12 | GRCh38.p7 | 13:27122822 | AACGTGGCCAGGCGC[A/G]GTGGCTCATGTCTGT | 219333 |
rs193004978 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158816 | TCAATATGATAGACA[C/T]TGAAGATCATGGGAA | 219333 |
rs193005751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27119911 | GCAGATGCAGGAGAA[A/G]CATGCTTATTGCATG | 219333 |
rs193035625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119639 | ACTCAACATTCTATC[A/G]TTTCCGATCACTTTC | 219333 |
rs193045819 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP12 | GRCh38.p7 | 13:27081201 | TGCTGTTTGACAGCA[C/T]TTTATCCACAGAACT | 219333 |
rs193087881 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27104639 | TGTGGGGAAAATGAA[C/T]AAATCTTCAACAAAC | 219333 |
rs193131612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27103976 | TTAATAAGGCCAAGA[G/T]AAATGTACTATTAAA | 219333 |
rs193137225 | snp | A/G | 0.0166325 | 0.0896639 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27066014 | TTGTTTTACACACAT[A/G]CAATTCTGTTCTAGG | 219333 |
rs193162452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146265 | AAATTAGCCAGGTGT[G/T]GTGGTGGGCATCTAT | 219333 |
rs193223269 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP12 | GRCh38.p7 | 13:27100611 | TTCCTGACGTGCATG[C/T]ACCTCAATCCCGTAC | 219333 |
rs193282556 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122360 | GAAGTGCCTTTCACC[A/T]CCTCCCATGATTCTG | 219333 |
rs193288549 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27085203 | TTTGAGATGGAGTCT[C/T]GCTCTGTTGCCCAGG | 219333 |
rs193302811 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155286 | CAGGGTTTCACCATG[C/T]TGGCCAAGATGGTCT | 219333 |
rs199537157 | snp | A/T | 0.495634 | 0.0465208 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163106 | AAAAAATACAAGCAA[A/T]TTTTGAAAAATCAAT | 219333 |
rs199538264 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142996 | TACTTGGGAGGCTGA[A/G]GCAGGAGAATCGCTT | 219333 |
rs199564197 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148140 | CTCAAAAAAAAAAAA[C/T]ACTTTTCTAAAACGA | 219333 |
rs199589608 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27110046 | TATTTTTTAAAACGT[A/G]CCTGCCACTTTGAGA | 219333 |
rs199655839 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167996 | TTAAAACAGAGCAAA[G/T]AAAAAAGAAAAGACA | 219333 |
rs199658395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162663 | TTACTGTTAAAGAGA[C/T]TGCCCTTTCATTTTA | 219333 |
rs199699456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104134 | CTCCTGGGCTCAAGC[A/G]ATCCTGCCACCTTAG | 219333 |
rs199829638 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160794 | TCTTTTTTTTTTTTT[-/C]TCCCCCTTCAACCTT | 219333 |
rs199839589 | in-del | -/A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27112288 | CATTTCATAGCTACT[-/A/T]TTTTTTTTTTTTTTC | 219333 |
rs199850735 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154329 | TCCATTTTTGTAACC[C/T]CTCATGCTACCAAGC | 219333 |
rs199874134 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27099697 | ACAATAATTTTTTTT[A/C]ACGTTCATTATTTAG | 219333 |
rs199912021 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129245 | TGGAAAGAACAAAGC[A/C]GCATCTCTGCCAGTC | 219333 |
rs199914478 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27086287 | TATATATAATTACAC[A/T]CACACACACACACAC | 219333 |
rs199932664 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27106840 | AACATTTACTTTGTA[-/C]CCCCTATCTTTTCTA | 219333 |
rs199976026 | in-del | -/T | 0.0225045 | 0.103662 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167541 | TTTGAGGTTTTCTTA[-/T]TTTTTTTTAAAGGCT | 219333 |
rs199979472 | snp | C/T | 1.65636e-05 | 0.00287776 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069237 | CCTTTCCAAAATAAC[C/T]AGAGAAGAAATGAGG | 219333 |
rs200006991 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27079219 | GCTCCCTGTGTGGGG[C/G]GGGGGGGAGTGGGGG | 219333 |
rs200019370 | in-del | -/GC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132455 | AAAGAAAAAGAAAAA[-/GC]AAAGGAACAGAAATA | 219333 |
rs200088270 | in-del | -/A | 0.0275645 | 0.114116 | intron-variant | USP12 | GRCh38.p7 | 13:27072115 | TACTTTTTTTTTTTT[-/A]AACTATGGAGGATGA | 219333 |
rs200089285 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101234 | GAATTTTGCTGTATG[C/T]GAAAGCAGCCATTAT | 219333 |
rs200105562 | snp | A/G | 1.65304e-05 | 0.00287488 | synonymous-codon | USP12 | GRCh38.p7 | 13:27090093 | ATACCTTAAGCAGTG[A/G]GTAATTGATGTATTT | 219333 |
rs200179207 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27083478 | CCAGGGACAGGAAAA[G/T]AACAACTGAAACAGC | 219333 |
rs200190013 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27083874 | TATATATATATATAT[-/A]TTTTTTTGAGATGAA | 219333 |
rs200196036 | in-del | -/AAG | | | intron-variant | USP12 | GRCh38.p7 | 13:27103761 | AAAAAAAAAAAAAAA[-/AAG]AGAGAGAGACAGAGA | 219333 |
rs200201514 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161908 | AAAAATAAAAAAAAA[A/T]TAAAAAGCCACTCAT | 219333 |
rs200217021 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164090 | ATCCCTACAAAAAGG[A/G]AAAAAAAAAAAATCA | 219333 |
rs200229060 | snp | A/G | 0.00199793 | 0.0315432 | missense | USP12 | GRCh38.p7 | 13:27095716 | ATATTACCATTAGGT[A/G]AACGACCATTTTGTT | 219333 |
rs200247192 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27121089 | ACAACAGGAGAGATG[A/C]GCATGAAGCCGAGAT | 219333 |
rs200306142 | in-del | -/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144749 | TTGTTTTTTGTTGTT[-/G]TTTTTTTTTTCCCCC | 219333 |
rs200347823 | in-del | -/TA | 0.014285 | 0.0832972 | intron-variant | USP12 | GRCh38.p7 | 13:27106845 | TTACTTTGTACCCCC[-/TA]TCTTTTCTAAAATAA | 219333 |
rs200417741 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150392 | AGAAAAAAACATTTC[A/C]GAGTTTCAAAACTCT | 219333 |
rs200455604 | snp | A/C/G/T | 0.000443494 | 0.0148857 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117784 | ACAGACAATCATAGC[A/C/G/T]TGTCACAGTTTCAAG | 219333 |
rs200525376 | snp | A/C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27093535 | ACCAAATGTCAGCAA[A/C/G]GATGTGGAGAAACAA | 219333 |
rs200552284 | in-del | -/ACT | | | intron-variant | USP12 | GRCh38.p7 | 13:27095256 | AAGGTAATCGTAGAA[-/ACT]AAAGGAAAAACGAAT | 219333 |
rs200552430 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143098 | CTCCGTCTCAAAAAA[A/G]GAAAAAAAAAAAAAG | 219333 |
rs200557295 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27095111 | AGTGAGCTGAGATTG[C/G]GCCACTGCACTCCAG | 219333 |
rs200575338 | in-del | -/AA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163104 | AAAAAAAATACAAGC[-/AA]ATTTTGAAAAATCAA | 219333 |
rs200621242 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27116334 | AAAAAAAAAAAAAAA[C/T]ATGTCAGGCAACTTT | 219333 |
rs200699701 | in-del | -/AA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130575 | ATCACAAAACATGCC[-/AA]AAAAAAAAAAAAAGG | 219333 |
rs200791954 | snp | C/G/T | 0.00835141 | 0.0640778 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154073 | ACAGAAATATCCACA[C/G/T]CTTTCCACTTTGCCT | 219333 |
rs200808709 | in-del | -/TT | | | intron-variant | USP12 | GRCh38.p7 | 13:27083874 | ATATATATATATATA[-/TT]TTTTTTTGAGATGAA | 219333 |
rs200843367 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27086288 | ATATATAATTACACA[C/T]ACACACACACACACA | 219333 |
rs200956953 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27099725 | TAGTTATTTTCATAT[A/T]TCCAAATCCATTCCA | 219333 |
rs200992971 | in-del | -/C | 0.0260105 | 0.111035 | intron-variant | USP12 | GRCh38.p7 | 13:27092196 | GGAAGAACTACCAAA[-/C]TCCAATGAAAGATAG | 219333 |
rs201005291 | in-del | -/A | 0.0205511 | 0.0992634 | intron-variant | USP12 | GRCh38.p7 | 13:27114214 | TACAATAAAACAATG[-/A]AAAAAAAAGCTATTC | 219333 |
rs201034927 | snp | C/T | 2.75972e-05 | 0.00371455 | intron-variant | USP12 | GRCh38.p7 | 13:27095589 | CTATACAAAATTGTA[C/T]GATATACTTACAGTT | 219333 |
rs201044910 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27093309 | GCCAAAATTATACCC[A/G]AAAAAAAAAACCCAC | 219333 |
rs201122357 | in-del | -/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157527 | CAACATATACATGCC[-/T]TTTTTTTAAAAAAAA | 219333 |
rs201146343 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158142 | AGTTACAATGAAGTC[A/T]TTAGGGTGGACCCTA | 219333 |
rs201159982 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143099 | TCCGTCTCAAAAAAA[A/G]AAAAAAAAAAAAAGA | 219333 |
rs201162177 | in-del | -/AAAC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147552 | TCATGTAAAAAAGAA[-/AAAC]AAAGTGTATGTCATA | 219333 |
rs201186004 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140960 | ATAGAAGATTCGAAG[-/A]AAAAAAAAAACACTG | 219333 |
rs201194475 | in-del | -/CA | 0.00874735 | 0.0655527 | intron-variant | USP12 | GRCh38.p7 | 13:27081353 | TCCATCTCAACAAAC[-/CA]CATTCTTTGATCTTC | 219333 |
rs201228103 | in-del | -/A | 0.0948562 | 0.196037 | intron-variant | USP12 | GRCh38.p7 | 13:27077907 | CACTGTCATTGTTTT[-/A]AAAAAAAAAAGTGGT | 219333 |
rs201262568 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27070505 | TAATTTTTTTTTTTT[-/T]AAAGCCAGGTCTGTT | 219333 |
rs201275843 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27087270 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGCG | 219333 |
rs201354369 | in-del | -/A/AA | 0.0689305 | 0.172377 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130537 | AGTTCTCACACACAC[-/A/AA]ACAAAAAAAATCACA | 219333 |
rs201448631 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27106712 | CCATTTATTTTTTTT[-/A]AAAAAAATGAGGAAG | 219333 |
rs201458126 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168463 | CCTCAACTGCAAAAC[A/C]CAGCCTCTCTACATG | 219333 |
rs201470801 | in-del | -/CT | 0.0240643 | 0.107019 | intron-variant | USP12 | GRCh38.p7 | 13:27083846 | GTTCTCGGGATGAAC[-/CT]TTTTGGGAGAATATA | 219333 |
rs201492095 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27122245 | TGAATCATCAGGGTG[G/T]TTCCCCCATACTGTT | 219333 |
rs201501770 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27093172 | CCTGGGCAACGAGAG[C/T]GAAACTCCATCTCAA | 219333 |
rs201523490 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27096144 | TTACCTGACTTATTA[-/T]TTCACAAATATTTCA | 219333 |
rs201544494 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27123103 | TCTCAAAAAAAAAAA[A/G]AAATATTTTACAGAG | 219333 |
rs201599655 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129244 | GTGGAAAGAACAAAG[A/C]AGCATCTCTGCCAGT | 219333 |
rs201600031 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27086286 | ATATATATAATTACA[A/C]ACACACACACACACA | 219333 |
rs201626049 | in-del | -/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167273 | GTCTCAAAAAAAAAA[-/T]AAAATAAATAAATAA | 219333 |
rs201634442 | snp | A/G/T | 3.39358e-05 | 0.0041191 | intron-variant | USP12 | GRCh38.p7 | 13:27090064 | ATTAAATTTCAAACT[A/G/T]AATAATTCTACATAT | 219333 |
rs201664330 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27109471 | GGAAAAGGCCAAGTT[G/T]GAAATGGGAATAGTC | 219333 |
rs201761075 | in-del | -/GA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163111 | ATACAAGCAAATTTT[-/GA]AAAATCAATGTAATT | 219333 |
rs201763509 | in-del | -/CTCT | 0.00874735 | 0.0655527 | intron-variant | USP12 | GRCh38.p7 | 13:27114290 | TTGTGGTTTAAATCA[-/CTCT]CTATCAGCTCTACTA | 219333 |
rs201772631 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27121307 | TGACTATGTGATCTT[-/A]AAAAAAAAAAAAAAA | 219333 |
rs201798774 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27070273 | TAATGATAGAAGTCC[A/T]AATAGCAGGCTCCAG | 219333 |
rs201798910 | in-del | -/A | 0.0685596 | 0.171987 | intron-variant | USP12 | GRCh38.p7 | 13:27108401 | GTGGGGGGAGAGGGG[-/A]AGGGATAGCATTAGG | 219333 |
rs201877202 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164088 | TTATCCCTACAAAAA[A/G]GAAAAAAAAAAAAAT | 219333 |
rs201888413 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27099696 | CACAATAATTTTTTT[C/T]CACGTTCATTATTTA | 219333 |
rs201900934 | snp | G/T | | | upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27172208 | GGGGAGGCGCGGGGG[G/T]GGCGGCGGCGATCTG | 219333 |
rs201902785 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27098376 | ATATTTAAAAAAAAA[A/C]CCTTTACAAAACAAG | 219333 |
rs201968995 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149658 | CCAAGGGGTGGTTAA[A/T]GAATACAAAATTACA | 219333 |
rs202032155 | in-del | -/A | 0.0174902 | 0.0918651 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157534 | TACATGCCTTTTTTT[-/A]AAAAAAAATATAAGT | 219333 |
rs202038577 | in-del | -/TG | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067224 | CTTTCTTAAACATGT[-/TG]TGATATAGCTAATGT | 219333 |
rs202057417 | in-del | -/CAA | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118114 | CACTGGGCATATGGT[-/CAA]CAACGCACCAGTACT | 219333 |
rs202083728 | snp | C/T | 8.27356e-05 | 0.00643125 | missense, intron-variant | USP12 | GRCh38.p7 | 13:27071141 | ATATAATGGCCTCGA[C/T]TGGGACCACTAAAAC | 219333 |
rs202090210 | in-del | -/TGTGTGTT | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117627 | CAACGTGTGTGTGTG[-/TGTGTGTT]TTTAATAGCACACGG | 219333 |
rs202096048 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27076746 | TGCCTCTAATAAGTG[-/A]AAAAAAAAAATCATT | 219333 |
rs202104426 | in-del | -/CT | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173262 | GCTCTTTTCTACCCC[-/CT]GTTTGGACAAGGGTT | 219333 |
rs202143353 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137076 | AAGATATTGAACAAA[A/G]ATAGTGAACAAACTG | 219333 |
rs202160951 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102014 | TTTCCCATTTTTTAA[C/T]GAATGAATGAATGAA | 219333 |
rs202216441 | snp | C/G | 0.00737488 | 0.0602748 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117729 | GAATTGGGAATGGGG[C/G]AAAGGAGAAAAAACA | 219333 |
rs202241953 | in-del | -/A | 0.0236746 | 0.106192 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134811 | GGGATATTAGCTAAC[-/A]AAAAAAAATTGTCAA | 219333 |
rs207473612 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163449 | CTCTTCTAAGAAGCT[G/T]TTTCCTGAAGCCCTC | 219333 |
rs367620846 | snp | A/C | 0.000165382 | 0.00909196 | synonymous-codon, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105882 | CGCAAGAACTTTTTC[A/C]CGAAATGGACGACAA | 219333 |
rs367748395 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129801 | CGGTCTTTTCAACAA[A/C]AAGAAAGCACCACTC | 219333 |
rs367779048 | in-del | -/AT | | | intron-variant | USP12 | GRCh38.p7 | 13:27083857 | AACCTTTTTGGGAGA[-/AT]ATATATATATATATA | 219333 |
rs367821269 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27107279 | GCAGTGAGCCAAGAT[C/T]GCACCACTGCACTCC | 219333 |
rs367883304 | in-del | -/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139385 | CTTTGGAAGGCGGAG[-/G]CGGGAGGATCACCTG | 219333 |
rs367930012 | snp | A/G | 6.73163e-05 | 0.00580117 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116594 | TGCCGAAGCATTGGC[A/G]CCCTATAAAATGAAA | 219333 |
rs368000511 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171054 | GAATGAGCGCTGCCC[A/G]CCCCGGCCGAGACCC | 219333 |
rs368015529 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | USP12 | GRCh38.p7 | 13:27122185 | TGTCCCCACACAAAT[C/G]TCACCTTGAACTGTA | 219333 |
rs368056168 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27091439 | GGATGCTCTAGATCA[C/T]CTGGGTGCATGAGTT | 219333 |
rs368081943 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145329 | GAACTATAGTAACAA[C/T]AGTGCTAAAACACAC | 219333 |
rs368179000 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27090835 | TTTCCCATTTTAATA[C/T]ATCAAAATTATTATT | 219333 |
rs368197971 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151573 | GATCCCGAGGGCCAG[A/G]AGTTCAAGACCAGCC | 219333 |
rs368246216 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126487 | GGTATTTTCATTATA[A/G]CTTTTCATGTTGGTA | 219333 |
rs368250744 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154443 | TGCTGAGACTGGTAG[A/T]GTGCTAACAGTACCT | 219333 |
rs368307191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27071160 | GACCACTAAAACAAA[C/T]GAAGAAGAAGTTAAT | 219333 |
rs368329039 | in-del | -/CAA | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124384 | TTATAAAGTAGAGAA[-/CAA]TACACCTTACCAAGA | 219333 |
rs368369085 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138978 | TCAACGGTAAGGTGT[A/C]TGATCATTCAGCCTT | 219333 |
rs368395439 | snp | C/T | | | upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27172254 | GGACCAGCTGCGACA[C/T]CCACCGCGGGCGAGG | 219333 |
rs368434115 | snp | C/G | 0.000307953 | 0.0124049 | missense | USP12 | GRCh38.p7 | 13:27075318 | GTTTTGTATATCGAT[C/G]AAGTTGATCCATATA | 219333 |
rs368441432 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27121335 | AAACCTCAGTAGAGA[A/C]TTCAAAGAAATCCTA | 219333 |
rs368443524 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144081 | TGGTGGCACATGCCT[A/G]TAGTCCCAGCCTCTC | 219333 |
rs368491412 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27079520 | GGGAGGAGCTGGAGG[A/C]AGGACTGACATTGCC | 219333 |
rs368520010 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101374 | TTCTTATGGTTTGCT[C/T]TCTTCTTTGCTAAGT | 219333 |
rs368603686 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27110828 | ATCTGGTTATATCAA[C/T]TGAAGAGAAGATACA | 219333 |
rs368656759 | in-del | -/AAT | | | intron-variant | USP12 | GRCh38.p7 | 13:27102043 | ATGAATGAATGAATG[-/AAT]GACAATAGGGATTGA | 219333 |
rs368705914 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27074721 | AAAGAAGATGAGAAG[A/C]AGACAGAAAGCAAAA | 219333 |
rs368707589 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150834 | TTTAACAACTGGCGC[C/T]GGGACAAATGGATAG | 219333 |
rs368719551 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146730 | TATTCCTTTAATTCA[G/T]CCGTTATGCATTGAA | 219333 |
rs368721509 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27106582 | ATAAAAAAGGAATGA[A/G]GATAATTCTCATATT | 219333 |
rs368871289 | snp | C/T | 5.97639e-05 | 0.00546611 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171582 | CGGCCGCCCGCTCGC[C/T]GCCACCTACCATGGT | 219333 |
rs368896667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082439 | TTGTGGCTAGTTTGA[C/T]CTTCTAACCAGGCCA | 219333 |
rs368896972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125188 | TATGTATGTATGTAT[G/T]GGGTTTCATATTATT | 219333 |
rs368897781 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27111332 | GAGTAGAGCCTTCAT[A/G]CAAAAGGTTTTCTGG | 219333 |
rs368903118 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155302 | TGGCCAAGATGGTCT[C/T]GATCTCCTGACCTCG | 219333 |
rs368906345 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP12 | GRCh38.p7 | 13:27123182 | CATGGTATACTACAA[A/G]TATCATTGAACTAGC | 219333 |
rs368911052 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116794 | TTCAGATGCACACTT[A/T]TTCCTGTGTTACGAT | 219333 |
rs368936454 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125594 | ACCTGGTTCATCTCA[C/T]TGGGACTGGCTGGAC | 219333 |
rs369011411 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27109116 | GCACTAAACAGTTGA[A/T]GAAGGAAGTTTCTGT | 219333 |
rs369026284 | snp | A/G | 0.000370751 | 0.0136102 | intron-variant | USP12 | GRCh38.p7 | 13:27105684 | ATTATGGCACACTAT[A/G]TTTAACCTTCCTAGT | 219333 |
rs369044569 | in-del | -/ACAA/ACACAA/ACACACAA | 0.0753466 | 0.180892 | intron-variant | USP12 | GRCh38.p7 | 13:27086308 | CACACACACACACAC[-/ACAA/ACACAA/ACACACAA]AATGCAGCACCTCCT | 219333 |
rs369068393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128663 | TTCTTGATAATTTCT[A/G]TATCTATTCCACCAA | 219333 |
rs369075387 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27108182 | ATGTGGCACATATAC[A/G]CCATGGAATACTATG | 219333 |
rs369103819 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101224 | GAATATGCCAGAATT[C/T]TGCTGTATGTGAAAG | 219333 |
rs369193114 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173672 | ACGTGGTGAAATCCC[A/G]TCTCTACTAAAATAC | 219333 |
rs369226169 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27109912 | GTGAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAG | 219333 |
rs369237467 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152679 | CGGGCGTGGTGGCTC[A/C]CGCTTGTAATCCCAG | 219333 |
rs369271226 | in-del | -/AAC | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124382 | TTTTATAAAGTAGAG[-/AAC]AATACACCTTACCAA | 219333 |
rs369294901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27072863 | CTGATAATGAGGCTG[C/T]GCACACCCTCCACAC | 219333 |
rs369411167 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27107099 | GGAGGCCGAGGCAGG[C/T]GGATCACTTGAGGTT | 219333 |
rs369435482 | snp | A/C | 7.09673e-05 | 0.00595639 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117775 | GGACCTCGCACAGAC[A/C]ATCATAGCGTGTCAC | 219333 |
rs369520401 | snp | C/T | 5.12046e-05 | 0.00505961 | synonymous-codon | USP12 | GRCh38.p7 | 13:27095640 | TTCATTAGTTAATGT[C/T]CCCTGAAAAATCTCA | 219333 |
rs369528874 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27080557 | TGGGGTCAGGCACAC[A/C]CGGAATAAAGGGAGA | 219333 |
rs369551411 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27099119 | TCCTATTTGGACATA[C/T]ATATTTAAGTGCATA | 219333 |
rs369658925 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173339 | TCACCATGCCCATCT[C/G]TGTGCCCGTCCTGAT | 219333 |
rs369691146 | snp | C/T | 3.34331e-05 | 0.00408845 | missense | USP12 | GRCh38.p7 | 13:27095666 | TCTCATGAACCCACG[C/T]TGGGTCTGGTGTGCT | 219333 |
rs369692707 | snp | A/G | 0.000164772 | 0.00907517 | synonymous-codon, utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069352 | ATCTGATGTCAACCC[A/G]TAGAATTCTTCAATA | 219333 |
rs369741932 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27122733 | ACAAGGTTAATATCA[C/G/T]ATAGTACTTTTTAGC | 219333 |
rs369743534 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27093877 | TATCAAGCCTTAAAA[A/T]GACATGGAAGAACCT | 219333 |
rs369808252 | snp | A/C | 0.00141324 | 0.0265447 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171544 | CCAGCGCCGCCCGCC[A/C]GCCCGAGAGGTCCCG | 219333 |
rs369845631 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27115417 | GGAATCACACACATC[A/G]CTTCAACCGCTTTCC | 219333 |
rs369878197 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160509 | TTAAAAAAAAAAAAA[A/T]GCAACACCAGACAAT | 219333 |
rs369914174 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27107791 | GAAAAAATGCTCATC[A/G]TCACTGGCCATCAGA | 219333 |
rs369926206 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152252 | CCATCAACGAACAAA[A/T]AAACAAAATGTAGTA | 219333 |
rs369958571 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27119503 | CCTCAGTGATTTTCA[A/G]AACTCCCAGTTCCAA | 219333 |
rs369966059 | snp | A/C | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066974 | CTGCATTAAGAAGAA[A/C]AAGTAAATGTAAAAC | 219333 |
rs370050337 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157935 | TTGGAACTTAAACAG[C/T]TTTGAATCTCTAGGG | 219333 |
rs370076279 | in-del | -/A/AA | 0.193 | 0.257658 | intron-variant | USP12 | GRCh38.p7 | 13:27078993 | AGTATGTCCTCTGAT[-/A/AA]AAAAAAAAAAACTAG | 219333 |
rs370135951 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135978 | ATGGGTTCTGCTGTA[-/G]GATTCTCAAATGATT | 219333 |
rs370187408 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27113583 | CCAATGGACGTCAGT[A/T]CCTCACCCTATGTTC | 219333 |
rs370187566 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27094956 | AGTTCAAGACCAGCC[C/T]GAGCAACACAGTAAG | 219333 |
rs370252199 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170951 | TCCACCTTCACACAC[A/G]CCCCTTTCCCCCAGC | 219333 |
rs370256322 | in-del | -/CA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167792 | TGAAGAGGAGACTTT[-/CA]CACACACACATTCCC | 219333 |
rs370282124 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27100603 | TAGGCAGCTTCCTGA[C/T]GTGCATGCACCTCAA | 219333 |
rs370285877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140242 | GTGACTGGAGGGAGC[A/G]AAACAGTGGTTTCAG | 219333 |
rs370350801 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136322 | GGCCAACATGGCGAA[-/A]CCCCATCTCTACTAA | 219333 |
rs370362095 | in-del | -/CTCCAA | | | intron-variant | USP12 | GRCh38.p7 | 13:27089010 | AGGAAAACGAGACAA[-/CTCCAA]ACTCCAATAAGGGAC | 219333 |
rs370385217 | in-del | -/TATA/TTTA | 0.473726 | 0.111565 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148676 | TCAAAAAAAAAAAAT[-/TATA/TTTA]TATATATATATATAT | 219333 |
rs370410376 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142880 | CAGGCTGATCACGAG[A/G]TCAGGAGATCGAGAC | 219333 |
rs370415590 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161061 | GTTTTGTGGAAAAGA[A/G]AATCCCCCTGCTCTA | 219333 |
rs370419417 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131596 | TAAATGGAAAAGAGA[C/G]CACTCTTTAACCTAT | 219333 |
rs370430441 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27070557 | TCCCTTGTTTTATTC[-/T]TTTTTTTTTTTTTTG | 219333 |
rs370456583 | snp | A/G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27120279 | ACATTTGAGAAGTAC[A/G/T]ACCCTATCAAAACTA | 219333 |
rs370535699 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27074316 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 219333 |
rs370541420 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27105577 | ATCTCCTTCACTAAA[A/C]GAGTGCCTCTTTGAA | 219333 |
rs370545275 | snp | A/G/T | 0.00113731 | 0.0238222 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171686 | CGGCGGCGGCGGGCG[A/G/T]GGGAGGAGGGGAGCC | 219333 |
rs370563244 | in-del | -/CCTCT | 0.0154538 | 0.0865337 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156255 | GGAATCTGGTTCAGG[-/CCTCT]TAATCTACCAGATTA | 219333 |
rs370583352 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164532 | TTAAATTTCTTATAG[C/T]TTACACTATCACAAA | 219333 |
rs370604949 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134734 | ATAGACGTCATAATA[C/G]ATAAGCCATCTTCAA | 219333 |
rs370619436 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27114126 | ATTTCACAGTACCCT[C/T]ACAAATGGACTTACT | 219333 |
rs370639445 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158213 | GACACAGGCATAGAA[A/G]GAAGACAAAATGGAG | 219333 |
rs370646626 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137849 | TTGCTCCCTGACTCC[-/C]TCATTGGCTTGGAAG | 219333 |
rs370646671 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27108677 | AAATGACATTTTAGG[C/T]TGGGTACAATGGCTC | 219333 |
rs370647080 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27088206 | CAGGCGGATCACGAT[A/G]TCAGGAGATCAAGAC | 219333 |
rs370661238 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130054 | GATGAAGGGAGAAGA[A/G]AGCACAGCATGCAAA | 219333 |
rs370668720 | in-del | -/ACAGTGTGGTAG | | | intron-variant | USP12 | GRCh38.p7 | 13:27092490 | GCTACGGTAATCAAG[-/ACAGTGTGGTAG]TGGGGAAAGAACAGA | 219333 |
rs370710296 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP12 | GRCh38.p7 | 13:27094742 | GTCTTTTTTTTTTTG[A/G]GAATATGCCTCCCTC | 219333 |
rs370714845 | snp | A/G | 0.000230791 | 0.0107397 | intron-variant | USP12 | GRCh38.p7 | 13:27075177 | CACTACTATGTCCCC[A/G]GAGTTGCAATTACCT | 219333 |
rs370737263 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155363 | TGGGATCACAGGTGT[A/G]AGCCACTGCACCCAG | 219333 |
rs370771962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169263 | GGGTTGGACAGGGGT[A/G]GGATTATTCAAGTAA | 219333 |
rs370841411 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149371 | ACTTCTACTCAATAC[C/T]GTACCATAGGTTCTA | 219333 |
rs370875187 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27085764 | GAATATGTGTATATA[C/T]ACACAAAACTGTTCA | 219333 |
rs370944464 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143561 | AAAAGCTATTGGTCA[A/G]CTGCCAAATCCCTCA | 219333 |
rs370956625 | in-del | -/TTTTTTTTAAG | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163115 | AGCAAATTTTGAAAA[-/TTTTTTTTAAG]ATCAATGTAATTCAA | 219333 |
rs370964463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27115940 | TATTAATACTAAATT[C/T]TGGCTATGAGAAATT | 219333 |
rs371014000 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068251 | CTAAAGATTGGTATA[C/T]CACCACTGCACCAGA | 219333 |
rs371069045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27100816 | AAGAAGAATAATCAG[G/T]GAGAACTAGTAAAAA | 219333 |
rs371087526 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146448 | GCTAAAGGCTAGGGG[A/T]ATAAGGTAGGGAGAG | 219333 |
rs371104703 | in-del | -/AC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142138 | AAAACACACACACAG[-/AC]ACACACACACGCAAT | 219333 |
rs371120321 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069084 | ACTGTACAGACAGCA[C/T]GATACCTGAGCAAAT | 219333 |
rs371224193 | snp | C/T | 1.68448e-05 | 0.00290209 | intron-variant | USP12 | GRCh38.p7 | 13:27105686 | TATGGCACACTATAT[C/T]TAACCTTCCTAGTAT | 219333 |
rs371307157 | snp | A/G | 3.33656e-05 | 0.00408432 | intron-variant | USP12 | GRCh38.p7 | 13:27116506 | TAAAAGCGTATCAAT[A/G]GATACTTACATTGAC | 219333 |
rs371388223 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134613 | TTGTCCAAGGAACTC[C/T]CATGAGCCTAAAAAA | 219333 |
rs371394267 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155323 | CCTGACCTCGTGATC[C/T]GCCCGCCTTGGCCTC | 219333 |
rs371473805 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27121644 | AGGCAGGTGGATCAC[A/G]AGGTCAGGAAATCGA | 219333 |
rs371477460 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173646 | TCAGGAGTTGGAGAC[C/T]AGCCTGGCCAACGTG | 219333 |
rs371480745 | in-del | -/TAGA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140947 | TTCCAATTAAAAAGA[-/TAGA]AGATTCGAAGAAAAA | 219333 |
rs371487632 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147997 | GCCAGGCGTGGTGGT[A/G]TGCACCTGTAGTCCC | 219333 |
rs371500980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27069517 | TCACACACAGCTGGC[A/G]GGGCACACCAAAAAA | 219333 |
rs371511871 | in-del | -/GACA | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117772 | CAAGGACCTCGCACA[-/GACA]ATCATAGCGTGTCAC | 219333 |
rs371532530 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27089812 | TTTCCTAGATTGTTT[C/T]TCTAAGCCCACCTCC | 219333 |
rs371629292 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117644 | TTAATAGCACACGGA[A/G]AGCAGACCGAAGAAT | 219333 |
rs371701380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27075124 | TGAATAATTCATGAA[C/T]ATCTTGAATGTACCC | 219333 |
rs371813508 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27102044 | ATGAATGAATGAATG[A/G]ACAATAGGGATTGAA | 219333 |
rs371874632 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27122489 | CACCCCATCTTTACC[A/G]AAAATACAAAAAACT | 219333 |
rs371932987 | in-del | -/TCTC | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140908 | AACGTCACACAAGAA[-/TCTC]TCTAACGCCTTTTGT | 219333 |
rs371997788 | snp | A/C/G | 3.37731e-05 | 0.00410921 | intron-variant | USP12 | GRCh38.p7 | 13:27090199 | ATTTTTTCAAATACT[A/C/G]GTAAACCACAGTTCC | 219333 |
rs372004335 | in-del | -/TG | | | intron-variant | USP12 | GRCh38.p7 | 13:27079210 | AATGTCGTGCTCCCT[-/TG]GTGTGGGGCGGGGGG | 219333 |
rs372033379 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139170 | ACCATACCTAACATG[C/T]AGACACACTTAACAG | 219333 |
rs372096170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125918 | AGGGGCGTCCGCCAT[C/T]GCTGAGGCTTGAGTA | 219333 |
rs372104358 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066378 | AGCCAGGACATGAGC[A/G]CTTTAGCCTCCCAGC | 219333 |
rs372111533 | snp | C/G | 0.000348371 | 0.0131933 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116623 | AAAACAAAAATCTTA[C/G]TATTTATAGTAGTCA | 219333 |
rs372196079 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27079553 | CAACCACCCTCAACC[A/G]GAATACCAACTACCC | 219333 |
rs372206059 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154020 | TTAGAGCTTCTTCTG[A/G]TACTATCTTTAACCA | 219333 |
rs372228460 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155283 | AGACAGGGTTTCACC[A/G]TGTTGGCCAAGATGG | 219333 |
rs372233687 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27080827 | ACTGTAGTGTATTAT[A/G]TAACAGCATTATGTC | 219333 |
rs372237566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27110428 | TGTCTGAATATGTTT[A/C]TTTTTTTCCACAGAG | 219333 |
rs372243839 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155238 | AGGCGCGTGCCACCA[C/T]GCCCGGCTAATTTTT | 219333 |
rs372252386 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171180 | TCCCCGACGACCCCG[A/G]CCCGGGGCCGCGCTC | 219333 |
rs372287111 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27071915 | TATATTTATTAAATT[A/G]TAATTCTATAATTAA | 219333 |
rs372290920 | in-del | -/TTTTTTTTTTTT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141023 | GTCACTTTTTTTTTT[-/TTTTTTTTTTTT]GAGATGGAGTCTTGC | 219333 |
rs372334706 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173156 | ACTGGATCTCCAAGC[A/G]CCTGCCTCCATGGAA | 219333 |
rs372387717 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27094744 | TCTCAAAAAAAAAAA[-/A]GACCATGTAAATGTT | 219333 |
rs372459431 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127842 | TTTAAATTTACTCAG[A/C]GGACTCCACTTATGT | 219333 |
rs372461160 | in-del | -/CAA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134591 | CTTCATTTTGAACAA[-/CAA]AGGGTTGTCCAAGGA | 219333 |
rs372461380 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27070557 | TTCCCTTGTTTTATT[-/C]TTTTTTTTTTTTTTG | 219333 |
rs372495823 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158457 | ATACATTCTGAGAAA[C/T]TGACTGTTAAGCAAT | 219333 |
rs372527345 | in-del | -/TTTTTTTTTTT | | | intron-variant | USP12 | GRCh38.p7 | 13:27081021 | GGCAATTTTTTTTTT[-/TTTTTTTTTTT]TGAGACGGAGTCTTG | 219333 |
rs372550949 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27074672 | ATTATAGGTATGTAC[A/G]TTCATACAGAGAAGA | 219333 |
rs372565812 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27105342 | TGCTCTCTATCTAAG[A/G]CTACTGCAAGGATCC | 219333 |
rs372608806 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147141 | AGCCATTCAATTTAC[A/G]GTATCTGTTAGGAAA | 219333 |
rs372680300 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116792 | TGTTCAGATGCACAC[A/T]TATTCCTGTGTTACG | 219333 |
rs372724653 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172367 | TGCACAGTTAAGATA[A/T]CCCGGGTATGCGTCC | 219333 |
rs372750018 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27098363 | TTAATATACAGAATA[-/T]TTTAAAAAAAAACCC | 219333 |
rs372764142 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27087552 | GTATTTATAAATACT[C/T]ATCTATCCTCTAGCT | 219333 |
rs372772860 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27108302 | AAAACCAAACACCGC[A/G]TGTTCTTACTCATAG | 219333 |
rs372774156 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27092094 | CTCATCTTCTACCAT[C/T]TTCTACCTGGCATAG | 219333 |
rs372781709 | in-del | -/ACCT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168122 | ACTCTCCTAGCACCT[-/ACCT]TTACCAGCTTTGGCC | 219333 |
rs372816554 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149562 | ATACATAGCCATCAA[C/T]TGTATTGATCTCATA | 219333 |
rs372827060 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152683 | CGTGGTGGCTCCCGC[C/T]TGTAATCCCAGCACT | 219333 |
rs372849567 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27098367 | ATATACAGAATATTT[A/T]AAAAAAAACCCTTTA | 219333 |
rs372945286 | snp | A/C | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067077 | ACCAGGAACTCAACA[A/C]ATACACTAGAACTTG | 219333 |
rs372952115 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136319 | CCTGGCCAACATGGC[A/G]AAACCCCATCTCTAC | 219333 |
rs372964546 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155455 | TATGTTACAGCCCCA[C/T]TGGAAACTAATGCAC | 219333 |
rs372968251 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27108101 | ATGTTTATTGCGGCA[C/T]TATTCACAATAGCAA | 219333 |
rs372969717 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124117 | ATTTTTACATAGTCA[A/G]TCATGGAAAACATAC | 219333 |
rs372985958 | in-del | -/AATAATAAT/TAATAATAAT | | | intron-variant | USP12 | GRCh38.p7 | 13:27103607 | ACTATCAAAAAAAAA[-/AATAATAAT/TAATAATAAT]AATAATAATAATAAT | 219333 |
rs373001651 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165902 | ACTCCCAAGATGTTC[C/T]AGAAATGGGCTACAG | 219333 |
rs373049354 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27077990 | AGGACAGAGAACATT[A/C/T]TTTTCCTTTTAAGTT | 219333 |
rs373140132 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130136 | CCTCCTAGAGCAGCT[A/G]CCTAGTAACAGGGCT | 219333 |
rs373205037 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141310 | GTGAGCCACCATGTC[C/T]GGCTGTGAAGTCACT | 219333 |
rs373323137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157066 | AGATTTCACAGTTTT[A/T]GTTTGGAAAAAATGA | 219333 |
rs373333528 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27109125 | AGTTGATGAAGGAAG[C/T]TTCTGTTTATAAAAT | 219333 |
rs373441155 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161494 | AAAACCCAGGTAGAC[C/T]AATACTGTAGAAATA | 219333 |
rs373445376 | in-del | -/AA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130561 | ATCACAAAACATGCC[-/AA]AAAAAAAAAAAAAAA | 219333 |
rs373478104 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148084 | CAGTGAGCTGTGACC[A/G]CACTACTGCACTCCA | 219333 |
rs373565496 | snp | A/G | 0.000282488 | 0.0118813 | synonymous-codon | USP12 | GRCh38.p7 | 13:27095694 | GCTGTTATTATTTTC[A/G]TTATCAATATTACCA | 219333 |
rs373636688 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159923 | AAAGAAAGTAGACTA[A/T]TAAAGCAACTAACAT | 219333 |
rs373771132 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145552 | CAAACTAGCTCCCAC[A/G]TTAACTTCAATCTAA | 219333 |
rs373802371 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27094436 | AGCCCAGGAGTCTTG[A/G]GGCTATAATGATCTA | 219333 |
rs373838238 | snp | A/C/T | 0.000247711 | 0.0111263 | intron-variant | USP12 | GRCh38.p7 | 13:27069407 | GTAAAATGTAAACAT[A/C/T]AGTACATAAATGAGC | 219333 |
rs373843327 | in-del | -/AAAAA/AATAATAA | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27103609 | TATCAAAAAAAAAAA[-/AAAAA/AATAATAA]TAATAATAATAATAA | 219333 |
rs373850556 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27094016 | CTCTTAGCTTTCTTG[C/T]TTGTGGACCCTATTT | 219333 |
rs373863078 | in-del | -/GTT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163604 | CTGGTTTTCAATCTT[-/GTT]CTCATCAGGACACAC | 219333 |
rs373917638 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132882 | GTGAAAGCCTGGCAA[A/C]CCAGCCACTCTGAAG | 219333 |
rs373938024 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27114786 | AAAAAAAAAAAAAAA[A/C]AAACTTGAGCAATAT | 219333 |
rs373943236 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27120016 | AAGATTATACTAAGC[A/G]ACTGGTTTCTGCTAA | 219333 |
rs373964622 | snp | A/G | 0.000132385 | 0.00813479 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069243 | CAAAATAACCAGAGA[A/G]GAAATGAGGCAGAAA | 219333 |
rs374058839 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138968 | TGTCACAGTTTCAAC[A/G]GTAAGGTGTATGATC | 219333 |
rs374060274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122001 | AGAACTAAATACAAC[C/T]TCAAAATATAAAAGT | 219333 |
rs374087243 | snp | C/T | 0.000129786 | 0.00805457 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171578 | GCCCCGGCCGCCCGC[C/T]CGCCGCCACCTACCA | 219333 |
rs374147037 | in-del | -/AGAAAC | | | intron-variant | USP12 | GRCh38.p7 | 13:27071227 | AATTTTGTTTTATAA[-/AGAAAC]AGAAACAGATAAATA | 219333 |
rs374196279 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27076537 | ATGGTAACAATTTTA[A/G]GTGATTATGGTTCTT | 219333 |
rs374220880 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148856 | TTGTCATGATAAAAA[-/A]CATAGAAAAGAATTC | 219333 |
rs374232745 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144751 | TGTTTTTTGTTGTTT[G/T]TTTTTTTTCCCCCAG | 219333 |
rs374297228 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167203 | GGAGGTGGAGGTTGC[A/G]GTGAGCCAAGATTGC | 219333 |
rs374300700 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143816 | TATAGAAAATATAAC[A/G]GATAGAAGAGCAAAT | 219333 |
rs374302593 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101195 | TTTGTAGTCCATTTT[C/T]CTTAGAGTATACTGA | 219333 |
rs374394894 | snp | C/T | 6.66767e-05 | 0.00577355 | missense, upstream-variant-2KB, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116589 | TCTAATGCCGAAGCA[C/T]TGGCGCCCTATAAAA | 219333 |
rs374398450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146421 | AAAAGCACCTATGTA[A/G]TAACGCACACGGCTA | 219333 |
rs374422254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140211 | CAATGTCCCCTGAAA[A/G]CAAAGATGTTGTGTA | 219333 |
rs374460833 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166022 | AGAATTTTAGACCTA[G/T]AAGGAGACAAGCATA | 219333 |
rs374465329 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27074707 | TATACCATGTTGGAA[A/C]AGAAGATGAGAAGAA | 219333 |
rs374541339 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27083565 | GCTTTAACCTCCCAT[A/G]GGATAAACGTATATG | 219333 |
rs374588130 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | USP12 | GRCh38.p7 | 13:27121657 | ACGAGGTCAGGAAAT[C/T]GAGACCATCCTGGCT | 219333 |
rs374588587 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142890 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCC | 219333 |
rs374635753 | in-del | -/AC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131934 | AATTGACACACACAC[-/AC]TACCTCCCAACTCTC | 219333 |
rs374652595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160903 | ACCCATCTCCCCGGG[A/T]TAAGCCCAGCATCCA | 219333 |
rs374691672 | in-del | -/ATAC | 0.0460142 | 0.144533 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136508 | GCCTCAAATAAACAA[-/ATAC]ATACATACATACATA | 219333 |
rs374728498 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159432 | CCATTTGCATCAGGC[A/G]TATAATTCTGGTGTT | 219333 |
rs374733222 | in-del | -/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140667 | AGTCAGCACTTCAAA[-/T]CCTAAACAGAGCAGA | 219333 |
rs374758847 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131043 | AGCTGAATGACACTC[A/C]AAGTTTATGTGTGGC | 219333 |
rs374759487 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27074943 | CTAACAGATCTCAAA[G/T]TTCTAGGAAATCAGA | 219333 |
rs374764557 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067410 | CTCTGTGGCATGTTG[A/G]TAGATCAGGCTGGCT | 219333 |
rs374768281 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | USP12 | GRCh38.p7 | 13:27098050 | GAGTGCAACTTCATA[C/T]AGTATTTTTAAAAAC | 219333 |
rs374863734 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27095049 | GGTCCTTGCTACTTA[C/T]GAGGCTTAGATGGAA | 219333 |
rs374875430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137911 | AGAGGGCCACATGGC[A/G]AGGAACCGTAGGCGG | 219333 |
rs374885952 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27072840 | CAAGCTGAACTGGAA[A/C]TGACATGCTGATAAT | 219333 |
rs374914316 | snp | A/C | 1.88375e-05 | 0.00306894 | intron-variant | USP12 | GRCh38.p7 | 13:27095834 | TGTCAAAAAGCTCTG[A/C]AAATAAAAACATTAT | 219333 |
rs374917585 | in-del | -/CTAA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127911 | TTCACTGCTAAATAA[-/CTAA]GCCAAAACCAACAGG | 219333 |
rs374932855 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27074172 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACGAGGT | 219333 |
rs374948699 | in-del | -/ACACACAC | | | intron-variant | USP12 | GRCh38.p7 | 13:27084170 | AATCCATGTTTGCAT[-/ACACACAC]ACACACACACACACA | 219333 |
rs374951733 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27074437 | AATCAGAGAGCTGGG[A/C]GGAGGGCTGAAGATG | 219333 |
rs374995334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27084791 | TTTTAATTACTTTAG[C/G]TTTGTAATATACTTT | 219333 |
rs375034776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27108995 | ATAATGACATTTTTT[A/T]AAAAAGCAGCCCTCT | 219333 |
rs375039882 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136468 | ATGCCACTGCACTCC[A/G]GTCTGGGCAACAAGA | 219333 |
rs375107900 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163557 | TGCATTTGTTTTATA[C/T]GTCCATCCTCTTCTA | 219333 |
rs375132796 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155114 | TGAGACGGAACCTCG[C/T]TCTGTCACCCAGACT | 219333 |
rs375135592 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170952 | CCACCTTCACACACG[C/T]CCCTTTCCCCCAGCG | 219333 |
rs375158333 | snp | C/T | 1.92784e-05 | 0.00310465 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116639 | TATTTATAGTAGTCA[C/T]GCACCACATAATGAC | 219333 |
rs375174132 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27080358 | AGGGGAATAAGATAT[A/G]GATCTAGTTAGGAAA | 219333 |
rs375183824 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27122143 | CCTGGGCAACATGGC[A/G]AAACCCCGTGATATG | 219333 |
rs375187351 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27121304 | CACTGACTATGTGAT[C/T]TTAAAAAAAAAAAAA | 219333 |
rs375211951 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162257 | TAAACGGCCTACCCA[A/C]GTGAAAATAATTAGT | 219333 |
rs375222785 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27069718 | TGTGGGAGGCCAAGG[C/T]GGGCAGATCACCTGG | 219333 |
rs375243517 | in-del | -/CTTT | | | intron-variant | USP12 | GRCh38.p7 | 13:27085180 | TTTCTTTCTTTCTTT[-/CTTT]TTTTTTTGAGATGGA | 219333 |
rs375248356 | snp | C/G | 3.29538e-05 | 0.00405904 | missense | USP12 | GRCh38.p7 | 13:27075252 | GATTGGTGGCATCAC[C/G]TGAAGTGTTAAACAG | 219333 |
rs375364999 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140956 | AAAAGATAGAAGATT[C/T]GAAGAAAAAAAAAAC | 219333 |
rs375410179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27085471 | CAGGCGTGAGCCACC[A/G]CATCTGGCCGTCAAA | 219333 |
rs375418030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27113603 | ACCCTATGTTCTTAC[C/T]CCACTGCCCCATGCT | 219333 |
rs375424305 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168461 | ACCTCAACTGCAAAA[-/C]CACAGCCTCTCTACA | 219333 |
rs375433385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139565 | AGGCTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 219333 |
rs375558098 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27070880 | TTCTAGGTGTGTAAA[G/T]GTTAGGTGACCACTC | 219333 |
rs375628083 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171986 | CTAATGCCCGGCCTG[C/T]CAGGCAGCGGCGCGG | 219333 |
rs375635306 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148819 | ACACACACACAAAAA[C/T]CAGGTGACAAAAATC | 219333 |
rs375660025 | snp | A/C/T | 4.98007e-05 | 0.00498982 | missense | USP12 | GRCh38.p7 | 13:27095707 | TCATTATCAATATTA[A/C/T]CATTAGGTAAACGAC | 219333 |
rs375671193 | snp | C/G | 0.00953873 | 0.0683987 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069110 | CAAATAAATCAACTA[C/G]CATGATCGGAAGGGC | 219333 |
rs375689507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27109476 | AGGCCAAGTTTGAAA[C/T]GGGAATAGTCTCTAG | 219333 |
rs375759075 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130547 | CACACACAAAAAAAA[-/A]TCACAAAACATGCCA | 219333 |
rs375818289 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27087063 | CAGACATCTGTACAG[C/G]CAGGAGAGGGGGAAG | 219333 |
rs375839854 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128217 | TCTGTAAATGTTCAC[A/C]ATGAGACAATGAGCT | 219333 |
rs375955948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144881 | CCCGGGTAATAGGGC[C/T]AAATCCTGTCTCTAC | 219333 |
rs376003463 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129447 | GCTATGCGTAGGCCA[A/G]GTGCAGTGGTTCATG | 219333 |
rs376014523 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152743 | GTCAGGAGATAGAGA[C/T]CATCCTGGTTAACAC | 219333 |
rs376021980 | snp | A/G | 0.000153988 | 0.00877327 | missense, upstream-variant-2KB, utr-variant-5-prime | USP12, USP12-AS2 | GRCh38.p7 | 13:27171608 | ATGGTACAGATGGAG[A/G]CGAATTTGGAGACTG | 219333 |
rs376028796 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27102774 | ATCACACAATTGATG[A/G]CTGTCTGCTTCCCCA | 219333 |
rs376037262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135478 | AGCACTTTCGGAGGC[C/T]GAGGCAGATGGATTA | 219333 |
rs376049541 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27082393 | TGAAGACAGGCCCTG[A/G]TTTTAGATTAGGCTT | 219333 |
rs376065361 | snp | G/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067764 | TTTACTGCCTGAAAA[G/T]AGTTTAATAAAGAAC | 219333 |
rs376072551 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27108466 | TGCAGCACACCAGCA[C/T]GGCACATGTATACAT | 219333 |
rs376107009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154420 | CCACTGCATCTTTAC[G/T]TTTCTCCTGCTGAGA | 219333 |
rs376135830 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27103599 | AACTATTGAACTATC[-/A]AAAAAAAAAATAATA | 219333 |
rs376166989 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124168 | TTTCACTCTGCCATT[A/T]TGAAAAAGATAAAAA | 219333 |
rs376209980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082854 | ATCTTTTTCTTTTTG[A/G]GACAGAGTTTCACTC | 219333 |
rs376230471 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27075507 | TTTTAATAGCCCAGC[A/G]ATGCCCAGTTTTGCA | 219333 |
rs376248182 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117950 | TTTGAAAGGGAAATA[A/G]AAGCAATTCTGTTAA | 219333 |
rs376255956 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159839 | AACATAAAATGGCAA[A/G]AACATCACGGTAGGC | 219333 |
rs376270291 | snp | C/T | 3.30033e-05 | 0.00406209 | missense, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105860 | TTTTCCTAGGTTGAC[C/T]CTTATACGCAAGAAC | 219333 |
rs376305441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169533 | ATACAGACACACCCA[A/G]TTTTAATAGTACCTT | 219333 |
rs376324044 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148795 | ACAGAATCATCTTAA[C/T]ACACACACACACACA | 219333 |
rs376435156 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069315 | AGAAAAGGATGTAAC[C/T]AGACTCAGAGTTCTT | 219333 |
rs376496030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155343 | GCCTTGGCCTCCCAA[A/G]GTGCTGGGATCACAG | 219333 |
rs376511506 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27091517 | AGGACAGTATTCCAC[A/T]TTTCAAAGTGGTTGT | 219333 |
rs376559888 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27100667 | CACCCACCCATTTCC[A/G]GGTCACAAATCTGGA | 219333 |
rs376564074 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143466 | AACATGAAAAAAACA[A/G]CAGAATTAGAAAAAT | 219333 |
rs376649999 | snp | A/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066477 | TATGTTATGAAAATG[A/T]GGTCTTTCTACTGCC | 219333 |
rs376658368 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27107725 | ATCTGCGATAAGAAA[A/T]GTACAATGTGCCTTC | 219333 |
rs376672232 | in-del | -/AAAT | 0.0655868 | 0.168795 | intron-variant | USP12 | GRCh38.p7 | 13:27122652 | TGAGACCCCATCTCA[-/AAAT]AAATAAATAAATAAA | 219333 |
rs376743343 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155657 | TATAACCCTGAGGCG[A/G]AACATATTAAAAAAT | 219333 |
rs376763060 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27118773 | ACACCTTAGGAAGGC[A/T]TTTCTGGCCTTTAAG | 219333 |
rs376799085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27111081 | GACTTGCTCATCTTC[C/T]GAATATAAAGCAACA | 219333 |
rs376832769 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27074405 | ACTCCATCTCAAAAA[A/G]AAAAAAAAAAAATTC | 219333 |
rs376836513 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154856 | GAAGCAGGACAGTCG[C/T]CGTCCGAGGGAGGTA | 219333 |
rs376862167 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27089127 | AAGACTAAAGAGACC[A/G]AATGCTAAATGTAAT | 219333 |
rs376865637 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160110 | ATGTGTCAATTATAC[C/T]TCAGTAAAGCTGGAA | 219333 |
rs376867865 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130254 | CTTTTGTTTCTGTCC[C/T]CTTAGGCTGCAACCT | 219333 |
rs376891726 | snp | A/T | 3.37724e-05 | 0.00410914 | intron-variant | USP12 | GRCh38.p7 | 13:27071029 | GTGAAAAGCAACATA[A/T]GCATACAACTTTCAA | 219333 |
rs376912289 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125983 | AAGCTTGAACTGGGC[A/G]GAGCCCACCACAGCT | 219333 |
rs376942634 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126167 | CAGACAGACTGCCTC[A/C]TCAAGTGGGTCCCTG | 219333 |
rs376948117 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116793 | GTTCAGATGCACACT[C/T]ATTCCTGTGTTACGA | 219333 |
rs377075802 | snp | C/G | 0.000526195 | 0.0162117 | intron-variant | USP12 | GRCh38.p7 | 13:27075438 | AAAGATATCCACCAT[C/G]TCCTTGAATTATCAA | 219333 |
rs377103958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27105554 | CTTGTATTAATTACT[A/G]TAAGACTATCTCCTT | 219333 |
rs377157194 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27110274 | ATCTTTGAGGTAAAT[G/T]GTATAATCATGTCAT | 219333 |
rs377200398 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27078670 | GAAATAAAGAATACT[G/T]CATAATAATGAAGGT | 219333 |
rs377212418 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161465 | TTTGAAAGTCTCTTT[G/T]CAGGGATCCCTGAAA | 219333 |
rs377276760 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076324 | ACAGGCTGTTCTTCA[C/T]GTTCTAAACAATCTT | 219333 |
rs377298353 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27122853 | AATCCCAGCACTTTG[C/G]GAGGCCGAGGCAGGC | 219333 |
rs377387978 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27100291 | CTCTCATTTGCTTAT[G/T]GCACCTTATTTCCTT | 219333 |
rs377420049 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068914 | AACATCATCTCCTTA[C/T]CAATACGGCACAGAT | 219333 |
rs377427374 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141325 | CGGCTGTGAAGTCAC[C/T]TTTTAAAACATTTCC | 219333 |
rs377431135 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27108819 | AAAAATTAGCCGGGT[A/G]TGGTGGCACGCACCT | 219333 |
rs377484968 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27101988 | CCGTGCCTGCCACAT[A/G]ATGAGATGTATTTCC | 219333 |
rs377493420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113909 | TTATAACCCAAAAAT[A/G]GAAAGTTTCATTTTT | 219333 |
rs377530347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157868 | TATCAAGTTTGTATC[A/G]GTTTACATTATTATA | 219333 |
rs377572317 | snp | A/G | | | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168989 | CATCTTCTCTCCACC[A/G]TTCCACACACACACA | 219333 |
rs377739205 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27113478 | ATTTTAGAACATTGT[A/G]TTTCCACATCCCCCT | 219333 |
rs377757164 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27073742 | GTAGCAGTAGCTAAG[A/C]GATTTACATCTCCCT | 219333 |
rs386378583 | in-del | -/TG | | | intron-variant | USP12 | GRCh38.p7 | 13:27079214 | TCGTGCTCCCTGTGT[-/TG]GGGGCGGGGGGGAGT | 219333 |
rs386378584 | in-del | -/AA | | | intron-variant | USP12 | GRCh38.p7 | 13:27094184 | TTGCAAGGGGATTTA[-/AA]AAAAAAAAAAAAAAA | 219333 |
rs386378585 | in-del | -/AA | | | intron-variant | USP12 | GRCh38.p7 | 13:27094198 | AAAAAAAAAAAAAAA[-/AA]AGTCATCATAAAGTG | 219333 |
rs386378586 | in-del | -/AAAA | | | intron-variant | USP12 | GRCh38.p7 | 13:27109913 | GAGACTCTGTCTCCA[-/AAAA]AAAAAAAAAAAAAGT | 219333 |
rs386378587 | in-del | -/AAAA | | | intron-variant | USP12 | GRCh38.p7 | 13:27109923 | CTCCAAAAAAAAAAA[-/AAAA]AAAGTCATCTTTGAG | 219333 |
rs386769326 | in-del | ATTT/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27096143 | CTTACCTGACTTATT[ATTT/C]CACAAATATTTCAAC | 219333 |
rs386769327 | multinucleotide-polymorphism | CATC/TCAG | | | intron-variant | USP12 | GRCh38.p7 | 13:27100077 | AACTCAAAAATCTTC[CATC/TCAG]CAGTCCACTCCATCC | 219333 |
rs386769328 | in-del | GAATG/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102031 | AATGAATGAATGAAT[GAATG/T]AATGAATGGACAATA | 219333 |
rs386769329 | multinucleotide-polymorphism | CA/TG | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155332 | GTGATCTGCCCGCCT[CA/TG]GCCTCCCAAGGTGCT | 219333 |
rs386769330 | multinucleotide-polymorphism | AA/TT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163105 | AAAAAAATACAAGCA[AA/TT]TTTTGAAAAATCAAT | 219333 |
rs386769331 | multinucleotide-polymorphism | GAAAA/TTAAG | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163111 | ATACAAGCAAATTTT[GAAAA/TTAAG]ATCAATGTAATTCAA | 219333 |
rs386769332 | in-del | CAG/GA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165334 | AAATTAGTGCTTTCT[CAG/GA]GGGTATATACTACTA | 219333 |
rs397718014 | in-del | -/A | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143112 | AGAAAAAAAAAAAAA[-/A]GAGTGAAAGAACAAT | 219333 |
rs397742607 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148139 | CTCAAAAAAAAAAAA[-/A]GACTTTTCTAAAACG | 219333 |
rs397826216 | in-del | -/A | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27093319 | ACCCGAAAAAAAAAA[-/A]CCCACTTAAAATTCG | 219333 |
rs397829798 | in-del | -/A | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27076047 | AAAAAAAAAAAAAAA[-/A]GAGTGGTAGAGGGAA | 219333 |
rs397829888 | in-del | -/A | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27098375 | ATATTTAAAAAAAAA[-/A]CCCTTTACAAAACAA | 219333 |
rs397943257 | in-del | -/GTGTGT | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117628 | AACGTGTGTGTGTGT[-/GTGTGT]TTAATAGCACACGGA | 219333 |
rs397944157 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156850 | GAGAGAGAGAAAAAA[-/A]TGATTTTATGGTTGT | 219333 |
rs397945330 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158158 | TAGGGTGGACCCTAA[-/A]TCCAGTGTGACTGGT | 219333 |
rs398022050 | in-del | -/TT | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27084516 | AAAACTATAGAACTC[-/TT]TTTTTTTTTTTTTTT | 219333 |
rs398022051 | in-del | -/A | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27098002 | GCAAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 219333 |
rs398022052 | in-del | -/A | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27099696 | TAAATAATGAACGTG[-/A]AAAAAAATTATTGTG | 219333 |
rs398022053 | in-del | -/T | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27120637 | GCTCCAGAGCAGAAC[-/T]TTTTTTTTTTTTTTT | 219333 |
rs398022056 | in-del | -/T | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156235 | AACCAGATTCCTTGA[-/T]TTTTTTTTTTTTTTT | 219333 |
rs398022057 | in-del | -/T | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164102 | ACCTGATGCTAGTGA[-/T]TTTTTTTTTTTTCCT | 219333 |
rs398022058 | in-del | -/A | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165069 | ACCTTATTTTATACT[-/A]AAAAAAAAAAAAAGC | 219333 |
rs398056215 | in-del | -/AAC | | | intron-variant | USP12 | GRCh38.p7 | 13:27083482 | GGACAGGAAAACAAC[-/AAC]TGAAACAGCCATCAA | 219333 |
rs398117126 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27094968 | CCTGAGCAACACAGT[-/T]AAGACCCCTGTCTCT | 219333 |
rs527243056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131462 | AGGTATGACTAGAAA[C/T]ATGAGTCATTTGGAT | 219333 |
rs527310674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124239 | AAACAATTCAATCTG[A/G]AATTAATGTAATTCC | 219333 |
rs527320226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073725 | TTTTTGTTAATAGAA[C/T]AGTAGCAGTAGCTAA | 219333 |
rs527356042 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166966 | GGCATGAATGATGAT[A/C]ATGATAACATGATAA | 219333 |
rs527377855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117900 | GTGGGGGATGACACA[C/T]AAGCAGATACAACTA | 219333 |
rs527403242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167929 | GCAGTAAGAAAAGGC[A/G]AACATTTTCCATGTA | 219333 |
rs527409186 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27094531 | AAATGGAGAAACACC[A/G]CCACCTTGACTGGGT | 219333 |
rs527415698 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27118660 | CTTATTCAAATGAGT[A/G]TAATCCTTTCCCCCG | 219333 |
rs527444327 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067230 | TTAAACATGTTGATA[C/T]AGCTAATGTTAAAAC | 219333 |
rs527446116 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130734 | AGCACGCTTACTTCC[C/T]CACGACTAACGTGGT | 219333 |
rs527496063 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125691 | GGGGTCAAGGGATTT[C/T]CCTTTCCTAGCCAAG | 219333 |
rs527499312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27111309 | AAGACCTAAAAATTA[C/T]CTTTCAAGAGTAGAG | 219333 |
rs527525750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155140 | AGACTGGAGTGCAGT[A/G]GCGCGATCTCGGCTC | 219333 |
rs527572176 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155293 | TCACCATGTTGGCCA[A/G]GATGGTCTTGATCTC | 219333 |
rs527609077 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153358 | AAAACTCAAATTCAC[G/T]TTTAAAGTCTTCAAT | 219333 |
rs527648996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27101573 | GAACTGACAGTCTAG[C/T]GGGAGAGACAGACAA | 219333 |
rs527653172 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27078395 | CCATGCATTTTGCTC[C/T]ATGTGAGGGTCCTGG | 219333 |
rs527669060 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158728 | GCACTTTGTTATGGC[A/C]GCCCTAGGAAACTAA | 219333 |
rs527671701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166513 | TCATCTCGCTGCAAC[G/T]GGCCAACATGGATCA | 219333 |
rs527733266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159293 | GTATCAATTACTAAA[G/T]TACAAGGGCGTATCT | 219333 |
rs527738389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27102308 | CAGTACCTGTAAAGA[C/G]AGGACTCCATTTCCT | 219333 |
rs527778213 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132343 | GTAACTTCAAACAAG[A/G]AAATTTTAGTTACAC | 219333 |
rs527799160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153515 | TGACAAGAGTGGAAA[C/T]GTCACTTCCATAACA | 219333 |
rs527821319 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160121 | ATACCTCAGTAAAGC[C/T]GGAAAAACTCAATAA | 219333 |
rs527863865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27096094 | TATATTGGCATAACA[A/G]ATACTGAGAATTTAA | 219333 |
rs527911727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139381 | AGCACTTTGGAAGGC[A/G]GAGGCGGGAGGATCA | 219333 |
rs527950677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27096702 | TGGGCAGCCTGACTC[C/T]ACCATGCCACACACA | 219333 |
rs527973719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130927 | TTTGCTTCAGCAAGC[C/T]GTGACGCTTAAAAAC | 219333 |
rs527981085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139947 | AAAGATGTTCTAACA[C/T]ACTTGTTTCTCAAAA | 219333 |
rs527987131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27080747 | CAATAAAGTGAAGAC[C/G]GCAATAAAGCAAGTC | 219333 |
rs527990006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27088900 | GGGATACTCCAACAC[A/G]TGGCACAAATCAAGT | 219333 |
rs528056551 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27119511 | ATTTTCAAAACTCCC[A/C]GTTCCAAATTTATCT | 219333 |
rs528062002 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163032 | AACAAGTTTTAACAA[C/T]CCACTGAACTGTCCT | 219333 |
rs528078919 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27116105 | ATCATGAGGTCAGGA[A/G]ATCGAGACCATCCTG | 219333 |
rs528144994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099133 | ATATATTTAAGTGCA[C/T]AGAAAAGGGTTTTTG | 219333 |
rs528209211 | in-del | -/AAC | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135338 | TCAAATCTCTATCGT[-/AAC]AACATTTATAAATTT | 219333 |
rs528216697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099769 | CAAATCAAATACAAT[A/C]ATATTAAGAATGCAA | 219333 |
rs528226585 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27170216 | CCTTCAATATGATTT[A/C]TTTAATACTGTCGAT | 219333 |
rs528268145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142930 | AAACCCCATCTCTAC[C/T]AAAAACACAAAAATT | 219333 |
rs528313053 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168652 | AAACAGGTATTTCAA[C/G]AGGTACCCTTGAAAA | 219333 |
rs528334562 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27093245 | TGAAAAACAAGTCAC[A/G]GACTGGGAGAAAATA | 219333 |
rs528386181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127855 | AGAGGACTCCACTTA[C/T]GTAATAAAAAACAAG | 219333 |
rs528390120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27077145 | GCTGATGAAAGTTTC[C/T]AGGTGACATAAGAAA | 219333 |
rs528471161 | snp | C/T | 0.000399281 | 0.0141238 | missense | USP12 | GRCh38.p7 | 13:27089907 | GCTTCCTGTTTGCTG[C/T]GACACTCTTCACAGT | 219333 |
rs528691260 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27110770 | TAAATCTGTCTTTAA[A/C]ATTGTATTTGTACTA | 219333 |
rs528694832 | snp | C/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066633 | ATTTCCAAGACAGAA[C/G]CCATGTGACTTAAGA | 219333 |
rs528717409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169600 | TGCCAACAATACACA[C/G]GCCCCACATGTAATT | 219333 |
rs528760882 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27091109 | ACAAGATAACTGACC[C/T]GAGTCTCAAAAAGTC | 219333 |
rs528785838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119887 | TAATGACACTGCGCA[A/G]CAGATTCTGCAGATG | 219333 |
rs528797203 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144933 | TCAGCCAGGCATGGC[A/G]GCATATGCCTGTAAT | 219333 |
rs528799953 | in-del | -/TGAG | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27111817 | TGAGAGCAATGAGAT[-/TGAG]TATTTTTGTAAAGGC | 219333 |
rs528801855 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162556 | GACAGATAGAGAAAG[A/T]CTAATAACAACAACA | 219333 |
rs528824534 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27113250 | TGACAGAGCAAGACC[C/G]TTTCTCAAAACAAAA | 219333 |
rs528831560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145223 | TTCCTTCTTGAAGAA[A/T]GACAGGTGGCCAAAA | 219333 |
rs528862773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27094821 | ATGTCCCCCTCTAAA[C/T]TGGATTCTGTACTGA | 219333 |
rs528876036 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27086986 | TAATCACTTAAAAAT[A/C]TGAGCTCTTCCCCTC | 219333 |
rs528892191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138344 | TAACAAAGATGTATG[A/T]ACAAGTCTATTAAAG | 219333 |
rs528895977 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135914 | CATCCCAAAACACAT[-/G]GAACTTTGTTTTAAC | 219333 |
rs528960099 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP12 | GRCh38.p7 | 13:27087456 | CTACAAGATTATCAC[C/T]GTGTATTCACGGTTT | 219333 |
rs528979423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130198 | GATTGTGCATTTTGC[C/T]CAGTTCTGGCAGTAG | 219333 |
rs528991924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152811 | GCCAGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 219333 |
rs528993911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119701 | CACAAAACTCCAGGG[A/G]AGTCTAAGACAACCA | 219333 |
rs528994926 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172766 | TTTATAAAATTCATA[C/T]TTGCACCCTGTTCTT | 219333 |
rs528999737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27079880 | AAGGACTGAATTCCA[C/T]GCCCTTTTAAAATGT | 219333 |
rs529033913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165782 | AACCTCCAGTTTTAA[A/C]GAAAGAAAAATGTAT | 219333 |
rs529041718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122647 | ACAGAGTGAGACCCC[A/G]TCTCAAAATAAATAA | 219333 |
rs529076911 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153536 | TTCCATAACAATAAA[A/C]AGCTGTGCTATCATC | 219333 |
rs529094379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166622 | AGGTAAGCAAAGCCA[A/T]ATGATATAAAATAAG | 219333 |
rs529100657 | snp | C/T | 0.000276191 | 0.0117481 | intron-variant | USP12 | GRCh38.p7 | 13:27116479 | TTTTAAAACTGCTTC[C/T]GAACATGATTCTAAA | 219333 |
rs529113774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073007 | AGCACCTGTTCTCAT[A/T]AGGGAAGTAGACATA | 219333 |
rs529132686 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170585 | TGGAAAACTGTGGTC[C/T]TTCTGGCCACGCACA | 219333 |
rs529229392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109873 | GAGATGGTGCCGCCA[C/T]TGCACTCCAGCCTGG | 219333 |
rs529232510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128374 | AAATATGACCAAACT[C/T]AGCATAAGAACATAC | 219333 |
rs529259258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27078216 | TTCAAAAAATAAATA[A/G]GTAAAAAAAATTTTT | 219333 |
rs529285961 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170946 | AAGTTTCCACCTTCA[C/T]ACACGCCCCTTTCCC | 219333 |
rs529296939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070679 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 219333 |
rs529312072 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155387 | CACCCAGCGACCTCC[A/G]TAACTTTAGAATAAT | 219333 |
rs529348681 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163843 | TCTGCTCTCACCAGA[A/T]AGGGACTGGCTAAGG | 219333 |
rs529350281 | snp | A/C/T | 0.000140857 | 0.00839121 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171585 | CCGCCCGCTCGCCGC[A/C/T]ACCTACCATGGTACA | 219333 |
rs529374125 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | USP12 | GRCh38.p7 | 13:27115552 | TATGCATTTTAAAAC[A/C]CCTGCCATGGATTCA | 219333 |
rs529392701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157466 | TACTTTTCATTAGCT[C/T]ATTTTTAGCAAAAAT | 219333 |
rs529431283 | in-del | -/T | 0.0158469 | 0.0875917 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142064 | AGGCAGAGGGTGCAC[-/T]TGAGCTGAGATCGTG | 219333 |
rs529512598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27101146 | AAACCAAAAAAATAA[C/T]CTTTAAACTTTTGTT | 219333 |
rs529600670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152963 | AAAAAAAAAAAAGAA[A/G]GAAAGAAAAGAAAAT | 219333 |
rs529601557 | in-del | -/TTTTTTTTTTT | 0.0995161 | 0.199636 | intron-variant | USP12 | GRCh38.p7 | 13:27081010 | GGGTGGCTGAGGCAA[-/TTTTTTTTTTT]TTTTTTTTTTTGAGA | 219333 |
rs529635131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27102089 | GACAGAAAAGTAGAT[C/G]TGCCCCCAAACAATA | 219333 |
rs529741524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119335 | ATCACTGTACTCCCC[A/C]ACACGGCCTAACAAC | 219333 |
rs529754163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160978 | AGGCCCCAGTGTGTA[A/G]CGTTCCCCTCCACAA | 219333 |
rs529758564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155185 | CTCCAAGGTTCAAGC[A/C]ATTCTCCTGCCTCAG | 219333 |
rs529765434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27112370 | GGCTCACTGCAGCCT[C/T]AACCTCCTGGACTCA | 219333 |
rs529765575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104787 | TAAAGGCAGGATTAC[A/G]CAATAGGGTATTTAA | 219333 |
rs529766932 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068545 | ATAAAAATATGTTCA[A/G]ATTTACTGACAGAAT | 219333 |
rs529866533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155329 | CTCGTGATCTGCCCG[C/T]CTTGGCCTCCCAAGG | 219333 |
rs529885371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27112945 | CATTACTTTGTTTAA[A/G]TACTGAGGCTAGGCA | 219333 |
rs529927720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142032 | AAGGCTGAAGCAGGA[C/G]AATTGCTTGAACTCA | 219333 |
rs529935457 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149800 | TTTCAGGATGAAACT[C/G]TTCTCAGATCACCAG | 219333 |
rs529983222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27098842 | GGAATGCTGGGCAAC[G/T]GTTAAAATGGAAACA | 219333 |
rs529993224 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | USP12 | GRCh38.p7 | 13:27083872 | AATATATATATATAT[A/G]TATTTTTTTGAGATG | 219333 |
rs530044908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27090902 | TGTCATACAACATGT[A/G]ACTATACAAAGTATG | 219333 |
rs530123120 | in-del | -/AAAT | 0.26518 | 0.249539 | intron-variant | USP12 | GRCh38.p7 | 13:27103607 | AACTATCAAAAAAAA[-/AAAT]AATAATAATAATAAT | 219333 |
rs530132717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27110682 | ATGTAACTACAGATA[C/T]ACTTCAATGAACCCT | 219333 |
rs530136512 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154280 | CATATACTCTGTTGA[C/G]CAAGGGCATATAGCA | 219333 |
rs530201055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147446 | CTAGCTAACAAAGTT[G/T]ATACATTATAACTGA | 219333 |
rs530202681 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27114994 | TCTACTAGCTCTGCT[C/G]CATCTACTCTGACCA | 219333 |
rs530251504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27096799 | AAAATTACCTATTTA[C/G]GACATTTTATTTTTA | 219333 |
rs530270308 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140090 | AAAGCTATTGACAAA[C/G]CTCATTTCAAGTTTC | 219333 |
rs530303307 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138338 | AAAATTTAACAAAGA[C/T]GTATGAACAAGTCTA | 219333 |
rs530323571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143626 | CTTATGATGAAGACA[C/T]TGGTGGTCTCCACTT | 219333 |
rs530330684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073931 | GAATCACTACACCAA[A/G]GTTCTTTAAGTAATC | 219333 |
rs530331508 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131974 | GCCACCTCCTAATTT[G/T]TATTACGTGTCACTG | 219333 |
rs530333503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140917 | CAAGAATCTCTCTAA[C/T]GCCTTTTGTAGCTAT | 219333 |
rs530338441 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27170002 | AGCCATGTGGCAAAA[C/T]TGTCACTGTAAAAGA | 219333 |
rs530389198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157206 | TGGTAATCATGTTTT[A/G]TTGGTTTTTTATTTT | 219333 |
rs530446539 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143827 | TAACGGATAGAAGAG[A/C]AAATTAAAAGACACC | 219333 |
rs530462002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125067 | AGTGAGTGGTGAGGT[C/T]TTTGCAGTGGACCAC | 219333 |
rs530493737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151054 | AAAAATCAGGCCAGA[C/T]GCTGTGGCTCACATC | 219333 |
rs530514220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143688 | TGATACAACTGCCAT[C/G]ATGTTCCACATGATA | 219333 |
rs530529465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27093304 | TAGTAGCCAAAATTA[C/T]ACCCGAAAAAAAAAA | 219333 |
rs530598731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27085815 | GTGTAAAAAATCTAA[A/G]TTGTTGGATTTAGAC | 219333 |
rs530738417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137314 | CATGATTATACATGA[C/T]AGATGTCATAATAAA | 219333 |
rs530763655 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142457 | TTAGATGACAGCATT[C/G]ATGTTTTAAATTATA | 219333 |
rs530792283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27091521 | CAGTATTCCACTTTT[C/T]AAAGTGGTTGTAAAG | 219333 |
rs530828737 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134724 | ATTGTACAAGATAGA[A/C/T]GTCATAATAGATAAG | 219333 |
rs530984625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162608 | AATACCTCAAAAAAA[A/C]TCTATTGTTAATTTT | 219333 |
rs530989873 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170298 | TAGAGAATCTGCTTT[A/T]TAAGGCATCTTTCAG | 219333 |
rs530993223 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | USP12 | GRCh38.p7 | 13:27084219 | ACACACACACACACA[A/C]ATTCCTGTCTGGGTG | 219333 |
rs531011300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126986 | TTCAGATGAGTCTTT[A/C]AAAAAACACAGTCCT | 219333 |
rs531021073 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27088374 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 219333 |
rs531032326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27075962 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 219333 |
rs531047637 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163061 | CTTGTACCCCATCCA[C/T]CTTGTTTTGTTGTCA | 219333 |
rs531109032 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27115601 | CAGTATAAAATAAAC[A/T]ACCACAACAATTATA | 219333 |
rs531112670 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156558 | GGCAGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 219333 |
rs531119033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27076851 | CTAGTGAATGAACTT[C/G]GCCTTTTGGAAACAT | 219333 |
rs531122102 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27104611 | CAATTAATCAAATTA[-/T]TCTACATGTGTATGT | 219333 |
rs531145442 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27112515 | TGGTCTCAGATTTCT[A/G]GGCTCAAAGCAATCC | 219333 |
rs531152893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113289 | AAACAAACAAACAAA[A/C]AAAAAACCCAGACAA | 219333 |
rs531154335 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27113535 | AGTAGACCAGACATT[A/G]AGTACCTCACCCAGA | 219333 |
rs531162543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130358 | GTCCAGAGATAGTAA[A/G]ACAGAAACTTCAGTG | 219333 |
rs531270738 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146443 | ACACGGCTAAAGGCT[A/G]GGGGTATAAGGTAGG | 219333 |
rs531289421 | in-del | -/A/AG | 0.0923359 | 0.194016 | intron-variant | USP12 | GRCh38.p7 | 13:27077690 | TATTGAAATGGCTCC[-/A/AG]AAAAAAAAGCAGAAA | 219333 |
rs531329812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166698 | AAACTAGAGTTTTCA[A/G]GCATATTAAAAATTT | 219333 |
rs531333760 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27122792 | ATGAAAACTCAAGTT[C/T]CGTTAAAAACAGGAA | 219333 |
rs531339966 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117112 | AGAAAAAGGAGAAAA[A/G/T]AAAGAATGATATTGA | 219333 |
rs531351213 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159645 | TATCTAAACTCAAAC[G/T]TTCCTACACCTTTAT | 219333 |
rs531362638 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27065805 | TGAAAACAGATTTTA[C/T]AGGAGCAATTACTAC | 219333 |
rs531367475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27080688 | GGCATATCTTGGACA[C/T]GCAGCAAGTTCAGTT | 219333 |
rs531442317 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160096 | CTTAAATACATACCA[C/T]GTGTCAATTATACCT | 219333 |
rs531453999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073074 | TAGCAATGCACGTCT[A/G]GTATTTATGTGAAGA | 219333 |
rs531477844 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125238 | TTTTTAAATTTTATA[C/T]ACAAAAGCATAAGAA | 219333 |
rs531487421 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27074941 | AACTAACAGATCTCA[A/G]AGTTCTAGGAAATCA | 219333 |
rs531505686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154364 | ATTTACTTACTTATC[A/G]AAAGTTGTAAAAGTA | 219333 |
rs531520680 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158571 | GCCTCTTGCTCCTAG[A/G]CCACAAACCTGTACA | 219333 |
rs531521312 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27121518 | CACAGGAAAAGAAAG[C/T]CCCATGAATAAGAGC | 219333 |
rs531539995 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157613 | AGTTTGAGGACAAAA[C/T]TACTGAAACATTAAA | 219333 |
rs531578412 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066481 | TTATGAAAATGAGGT[A/C]TTTCTACTGCCATCA | 219333 |
rs531591979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27071477 | TTTTTCTATCATTTT[A/G]TAAGGGAGGGGATCA | 219333 |
rs531594819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27110753 | TTACCCAGTATCCAG[C/T]ATAAATCTGTCTTTA | 219333 |
rs531648774 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27078917 | TTCTCAAGTTCAACC[A/G]AAACATTCACTAATG | 219333 |
rs531654372 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27108813 | AATTACAAAAATTAG[A/C]CGGGTGTGGTGGCAC | 219333 |
rs531671706 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163155 | ATATTTTTACCAACT[C/T]CATTGTTTCTTATAT | 219333 |
rs531690942 | in-del | -/AATT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124240 | AACAATTCAATCTGG[-/AATT]AATGTAATTCCTTAA | 219333 |
rs531714635 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135391 | TATCTCAATCCCTAA[A/C]CATTTATATACTCAA | 219333 |
rs531738708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109314 | ACAACTGAATATTGT[A/G]TGTCTTTTAATATAT | 219333 |
rs531776067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27102194 | AGGCCCACCTAAAAT[G/T]ATCCCAAACAGTCCA | 219333 |
rs531791869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27116237 | GAATGGCGTGAACCC[A/G]GGAGGCAGACGTTGC | 219333 |
rs531812835 | in-del | -/AAT/T | 0.0092923 | 0.0675263 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167274 | CTCAAAAAAAAAATA[-/AAT/T]AAATAAATAAATAAA | 219333 |
rs531831496 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140896 | CTGAACTTCAGAAAC[A/G]TCACACAAGAATCTC | 219333 |
rs531835755 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163280 | ACTTCTTTAAATATG[A/C]CCCCTTCCTACTCTC | 219333 |
rs531845514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152553 | TAAAACTGACTGTGG[C/T]GATAAATGCAAAACT | 219333 |
rs531845621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158526 | AACCTAGATGGTACA[A/G]CCCACTACACACTTA | 219333 |
rs531884956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27095043 | GCTCGTGGTCCTTGC[C/T]ACTTATGAGGCTTAG | 219333 |
rs531905513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138448 | GTGTATCCCCTGTAT[C/T]GCCCTCCAGAAAACA | 219333 |
rs531920017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27087550 | GTGTATTTATAAATA[C/T]TCATCTATCCTCTAG | 219333 |
rs532034893 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27105595 | GTGCCTCTTTGAAGA[A/G]AGGCGTGTCATCCTT | 219333 |
rs532041554 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27096051 | ATACTACTAATTGAT[A/C]CTGAGAAAAGGGCAA | 219333 |
rs532068022 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP12 | GRCh38.p7 | 13:27113186 | CTGCAGTGAGCCAGG[A/G]AGGCGAAACTGCAGT | 219333 |
rs532165466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27097422 | GTGAGCCGAGATTGC[A/G]CCATTGCACTCCAGC | 219333 |
rs532165656 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27119763 | AAGAATGATGGCTAG[C/G]ACAGACTGACGGTAG | 219333 |
rs532252601 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149219 | ACGGAATTAATAAAA[A/T]AAAAGAGGAAAAGAG | 219333 |
rs532280180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27092448 | GTCAGAGGACTGAGA[C/T]TACCTGACTTTAAGA | 219333 |
rs532296914 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142865 | TTTGGGAGGCCGAGG[A/C]AGGCTGATCACGAGG | 219333 |
rs532317375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149968 | ACACTCACCTTCTGC[C/T]GTACAGCCCGGTTCC | 219333 |
rs532405543 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117062 | CCTGTAAAAAAAACT[A/G]TCTGTGATCCCTATT | 219333 |
rs532410351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27091785 | CAAGGAATGAGACTG[A/G]AAAGGAACCCTCATA | 219333 |
rs532448047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27084302 | CACAAGGTCAAAAGA[C/T]TGAGACCATCCTGGC | 219333 |
rs532492724 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154311 | TAGGTTTTATTCATT[C/T]CATCCATTTTTGTAA | 219333 |
rs532524315 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076699 | AAGCAAAATACTCCT[C/T]ACAATTTAAAGAAGT | 219333 |
rs532575995 | in-del | -/AT | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172498 | AAGAACAAATTACAC[-/AT]GTTTAACTCTTTGAA | 219333 |
rs532581083 | in-del | -/AAG | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163780 | CTTAAAAAAAAAAAA[-/AAG]AAAAAGAAAAAAAAA | 219333 |
rs532591461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27090721 | AGACATAAATCTTCC[C/T]AGCTATTTCCTTCAG | 219333 |
rs532602043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074411 | TCTCAAAAAGAAAAA[A/C]AAAAAATTCTAATCA | 219333 |
rs532626361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27097468 | AAAACTCCATCTCAA[A/C]AACAACAACAACAAA | 219333 |
rs532627220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082985 | GGATTATAGGCATGC[A/G]CCACCACGTCCAGCT | 219333 |
rs532654298 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165912 | TGTTCTAGAAATGGG[A/C]TACAGAGCAAAAAAA | 219333 |
rs532685727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27075096 | AATACAGAATTTCTA[A/G]AAGTTCTATATATGA | 219333 |
rs532689539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27118846 | TGTTAGCCGAATCAC[A/G]TGCCACTCGCCTTGT | 219333 |
rs532697967 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164035 | ATAATGTAGGTCTCC[A/G]TGAATCCTTCCTCAA | 219333 |
rs532700650 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27110492 | ACAGGAGTTACCAAC[C/T]TTTTGAAGAGGCTTG | 219333 |
rs532713816 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124309 | AACCAGATTATGGCT[-/A]AAAAAATGGTGTCTA | 219333 |
rs532733810 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082347 | AAATTTTCTTCTGCA[C/G]CTTCCTTACCTCTCT | 219333 |
rs532762131 | in-del | -/T/TT | | | intron-variant | USP12 | GRCh38.p7 | 13:27081020 | GCAATTTTTTTTTTT[-/T/TT]TTTTTTTTTTTGAGA | 219333 |
rs532771055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125130 | CACACATCTTTATTA[A/G]GAGTAAACAAAGTCT | 219333 |
rs532865432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27169079 | CTTTTATACTGAATG[C/T]AGAACTTGGTACTCC | 219333 |
rs532881814 | in-del | -/T | 0.184838 | 0.241358 | intron-variant | USP12 | GRCh38.p7 | 13:27112456 | AAAATGCTCCCAGCA[-/T]TTTTTTTTTTTTAAG | 219333 |
rs532882245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137523 | GATGTATACTTAAAT[A/G]AAAGTAGACATGTTC | 219333 |
rs532885839 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124839 | CTTAACCCTCATACC[C/T]GTTCTAGAAAACACC | 219333 |
rs532907909 | snp | C/G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27072334 | TGGGGTAAGGACTGG[C/G/T]AAATTGAAAAAAGTT | 219333 |
rs532940738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129272 | AGTCCTGTTTTCTAG[A/C]CCTCGATTCCCCTGA | 219333 |
rs532957027 | snp | C/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171948 | CCCGCCCAGCGCACA[C/G/T]GGGAGCGGGCTCCGC | 219333 |
rs532979265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27079153 | TTTTAGGTCCTGTTC[C/T]CTAGAGCAGACCCTG | 219333 |
rs533017531 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172653 | CCAGCAGTGATGATG[A/G]TATTACCAGAGACAG | 219333 |
rs533113420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127082 | AGAGTCTTGGTCTAT[A/G]CTTCCTCCTCTAGTG | 219333 |
rs533129525 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135871 | AAACATGCTTTTCTT[C/T]ACTTTCCAAGTTGAA | 219333 |
rs533140842 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132082 | GTAAGAAATCCGGGC[A/T]ATGAAACAAAAGGAA | 219333 |
rs533155805 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155974 | TTAAAAATATTTCTT[-/A]AAAAAAACCTATAGA | 219333 |
rs533168998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27085099 | ACAAGTCTTCTGCCA[C/T]GTAAGTTTATTCCTA | 219333 |
rs533172314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129894 | TCCAAAACATACGAG[C/T]GGAGTGACCAACATG | 219333 |
rs533189276 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27079663 | GTCAGAAACGTTTTT[A/T]AAAGTAAATTTCCTA | 219333 |
rs533246667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27120555 | GCTATTCAGGAGGCT[A/G]AGGCTGCAGTGAGTC | 219333 |
rs533282599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27121409 | CAGAATTACAAATTC[A/G]CTCTGGAATGAGACA | 219333 |
rs533297195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27116336 | AAAAAAAAAAAAAGA[C/T]GTCAGGCAACTTTGT | 219333 |
rs533337187 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156634 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 219333 |
rs533380267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27114782 | TTTAAAAAAAAAAAA[A/C]AAACAAACTTGAGCA | 219333 |
rs533398632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27077032 | CCTATTAGAGTTCTT[C/T]TACATTGTAAAAAAT | 219333 |
rs533418107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27107973 | TGTGGAAGTCAGTGT[A/G]GTGATTCCTCAGGGA | 219333 |
rs533425691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170380 | ATGGAAAATTTCTTG[C/G]GGATCTCCTATATGA | 219333 |
rs533426563 | in-del | -/TTAT | 0.00557542 | 0.0525036 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158725 | TGGCACTTTGTTATG[-/TTAT]GCAGCCCTAGGAAAC | 219333 |
rs533457371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151659 | TAGAGGCATGCACCT[A/G]TACTCCTAGCTACTC | 219333 |
rs533486863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070143 | AAAAGAACTACTATT[A/T]CCGCAGGCAACAAGA | 219333 |
rs533488969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170777 | GATGTGTCTGGTGGG[C/G]TGAAGTAAACAAATG | 219333 |
rs533499030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113741 | CAGAGGACCTGGGCC[A/G]GAGCTCTTTTCCCAG | 219333 |
rs533504271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123541 | ATCTTGAATTGTAGC[C/T]CTCATAATTCCCACG | 219333 |
rs533510460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116768 | CTGTACCTTTCTTAC[A/G]TTTAGATATGTTCAG | 219333 |
rs533522518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070577 | TTTTTTTTTTGAGAC[A/G]GAGTTCACTCTTATT | 219333 |
rs533548089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117197 | ACAGAACCAAAGCCT[A/G]GATCAAGGAATTACA | 219333 |
rs533549431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158947 | TTTGGGGGGAGTGGG[A/G]GTGACACACACACAA | 219333 |
rs533553219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073181 | AAGGCATGAGGCAAT[A/G]AGAGTGAGACAGGAG | 219333 |
rs533573866 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27083747 | CATGAATATTTAGAT[-/A]AAATATTATAAAGCA | 219333 |
rs533715857 | snp | A/G | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27100470 | CCAAGATACAGCCAT[A/G]CTATGACCCTCAACC | 219333 |
rs533752675 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27095288 | AATATGCCTCCCTGA[C/T]CTGTATGATCCTATG | 219333 |
rs533765218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27103903 | ATTTTACCTCTGTTC[A/G]GCATGAGGGTCAATC | 219333 |
rs533785229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139637 | ATAAAAATATAGTCA[A/C]TCTTGTATAAACTGA | 219333 |
rs533785349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147750 | TAATATATTCAAAGC[A/G]CTCAAAGAAAGGAAA | 219333 |
rs533844756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140332 | TTGTCTGAAAACTCA[C/T]TGAAGTTTACATTTA | 219333 |
rs533857283 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27077240 | TTTTATTAAACCCAC[-/AT]AGAGTTACTGAAAAG | 219333 |
rs533877617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109987 | CTGCATTGGATGATA[C/T]TAAGAAATTGTTGAC | 219333 |
rs533917370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27103076 | CCAGGACCATCAAAA[A/C]GATTAGTAACATAAA | 219333 |
rs533932514 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27070363 | TGCGGTGTTGAAAAT[A/G]AATTGTATCTTGACC | 219333 |
rs533947925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27101650 | TATAGCTGCAACAAT[A/G]ATGCAAAAAAAAATG | 219333 |
rs533958508 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP12 | GRCh38.p7 | 13:27075886 | AATACAAAAAATAGC[C/T]GGGCATAGTGGCAGG | 219333 |
rs533996936 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068921 | TCTCCTTATCAATAC[A/G]GCACAGATTCCGATT | 219333 |
rs534030093 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27100618 | CGTGCATGCACCTCA[A/G]TCCCGTACAATTCAA | 219333 |
rs534034028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27096945 | ATTTTAGAAGAGATA[C/T]AGATATGACTACATA | 219333 |
rs534046008 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137860 | CTCCCTCATTGGCTT[G/T]GAAGGAGCAAGCTGC | 219333 |
rs534087367 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27092122 | AGTTGGTGCTTAGCA[-/C]CCCCCCAAAATGAAT | 219333 |
rs534105174 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP12 | GRCh38.p7 | 13:27087598 | GCTCAGGAACAATGA[C/T]ATCCCAATAGCAACG | 219333 |
rs534106221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129600 | TAGTCCCAGCTGTTC[A/G]GGAGGCTGAGGCAGG | 219333 |
rs534120269 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27082648 | CTTAATCATTTCTAG[A/C]TTTTCACTTAAAGTG | 219333 |
rs534124649 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27120796 | ACTATAGAATTCATC[A/T]TGAAGAAGTAATGAG | 219333 |
rs534146848 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128498 | TTTAAAACATAACTA[C/T]ATCTGAACTCCGTAA | 219333 |
rs534166324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152684 | GTGGTGGCTCCCGCT[G/T]GTAATCCCAGCACTT | 219333 |
rs534218730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122796 | AAACTCAAGTTTCGT[C/T]AAAAACAGGAAACGT | 219333 |
rs534257992 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27106516 | ACTGGCTCTAAAAGC[C/T]ATAAAACAGCTAAAA | 219333 |
rs534300504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145706 | TAAAGTTGTTTATCT[A/G]GTTGTCCTAAAGTCC | 219333 |
rs534301094 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125898 | CGCTGGAGCTTGGCA[-/G]GGGGAGGGGCGTCCG | 219333 |
rs534321095 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129439 | ACTCTAAAGCTATGC[A/G]TAGGCCAGGTGCAGT | 219333 |
rs534335585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27098404 | AAGAAAAAAAATTTT[A/T]AAAACTGGCAAAGGA | 219333 |
rs534366903 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27090987 | AGTTGAAGGGAGTTC[C/T]AATGGTGATTTTGAC | 219333 |
rs534386253 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27172250 | GAGGGGACCAGCTGC[C/G]ACACCCACCGCGGGC | 219333 |
rs534405366 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27084662 | ATCCTTTTCCCACTA[C/T]GTATTCATTCTTAGC | 219333 |
rs534412169 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126358 | GGAGTGGACCTCCAG[C/T]AAACTCCAACAGACC | 219333 |
rs534427786 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124862 | AAAACACCATGTGCC[C/G]AGAAACTGAATCAAA | 219333 |
rs534449472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27083585 | AAACGTATATGACCA[C/T]TAGAGTGACATTTCC | 219333 |
rs534491892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135232 | AGGTTGCAGTGAGCC[A/G]AGACCACAAAACCTG | 219333 |
rs534496839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27072721 | AGGGATGGGAAATCA[C/T]GAAATGGTGCCCAGT | 219333 |
rs534514282 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166246 | AGTTTCTGGAATAGA[C/G]CTGCTAAAAGAGAAA | 219333 |
rs534528507 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173743 | GCTACTCAGGAGGCT[A/G]AGGCATAAGAATAGA | 219333 |
rs534579823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27076314 | ACTGTGAAACACAGG[C/T]TGTTCTTCATGTTCT | 219333 |
rs534581454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27120039 | TCTGCTAAGTTGTTT[C/T]TAAATTTAACAGTGT | 219333 |
rs534615654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27069618 | GTACAGGATGAATTA[C/T]ATGAAACCACTAATA | 219333 |
rs534626351 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139026 | ATTAACCAGTATCTT[C/T]CCAAGGAAGATTCTT | 219333 |
rs534652672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142255 | AGCAGCCAAACCCAA[A/C]CTGAGGAACGGTATA | 219333 |
rs534740434 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144376 | GGTGCATACCTGTAA[C/T]ATTAGCTACTCAAGA | 219333 |
rs534743958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132861 | GACTCTAGCCTTATC[C/T]TAAAGGTGAAAGCCT | 219333 |
rs534751171 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167604 | TAACACAGCAAAATT[A/T]GATAAGTAAAACAAT | 219333 |
rs534753345 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148142 | CAAAAAAAAAAAAGA[-/C]TTTTCTAAAACGAAA | 219333 |
rs534790774 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126418 | CAAACAAACAGAAAG[A/G]AATAGCACAAACAGA | 219333 |
rs534792863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27075727 | CTAAATGCACGGGGT[A/G]CTCAAGAGTGGTAGA | 219333 |
rs534794188 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067013 | CACAATCCCTCCCCT[A/G]ACAAATCATACTATG | 219333 |
rs534807671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074475 | TGTAACTTTTTTTAT[C/T]TGGATAAAACATGCT | 219333 |
rs534868939 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166903 | CCACCTCATCATTTT[A/G]TAACATTAAACTCAT | 219333 |
rs534932312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170422 | TAAATAGGGCCAGTG[A/C]GGCATGAAACACAAG | 219333 |
rs535033875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27105695 | CTATATTTAACCTTC[C/T]TAGTATGTCATTAAT | 219333 |
rs535073574 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171251 | GCGCGCCTCGGCCCT[A/C]GTCCCCGCGTCCCGA | 219333 |
rs535099547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118232 | TTTCCTGACAGCTCT[A/G]GGCTGAAAAGGGGAC | 219333 |
rs535117439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27121792 | CGCGAACCTGGGAGG[C/T]AGAGCTTGCAGTGAG | 219333 |
rs535199030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161122 | AGTCCCAGCTACTAC[C/T]CCCAAGGTACCACCT | 219333 |
rs535232382 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27087034 | ATTCAACTATTTGAT[A/G]GGGCCAAATAACACA | 219333 |
rs535233933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27111684 | CTTACACATTTATAA[A/G]TTATACATACTATGT | 219333 |
rs535274454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158318 | GGGTAGAAAATGGAA[A/G]AGAGTCTCCTCATAG | 219333 |
rs535308622 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158731 | CTTTGTTATGGCAGC[A/C]CTAGGAAACTAATAA | 219333 |
rs535316676 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP12 | GRCh38.p7 | 13:27104992 | CCACATTAGATAGAA[C/T]ACTGGGCTTACATAT | 219333 |
rs535325541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27112865 | TATTTTCTTCCTATT[C/T]CCAATGGATCATCTT | 219333 |
rs535339051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148693 | ATATATATATATATA[A/G]TATAAATAATAATAA | 219333 |
rs535375389 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27101769 | TTTGGAGAAAAAGAA[A/T]TGTTTGAAATAAACA | 219333 |
rs535411919 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27094624 | CCCGAGAAAAACACA[A/T]CATGAATGATATATT | 219333 |
rs535420879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113409 | GTTCTGTGAACATGC[G/T]AAGATGTTCTAAGGG | 219333 |
rs535422706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27120792 | CCTTACTATAGAATT[C/T]ATCATGAAGAAGTAA | 219333 |
rs535441612 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127483 | ACATGATCAAAGGGC[C/T]TTTGCCTCTATTCCT | 219333 |
rs535444904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129390 | AACCATTCTTAGTAA[A/C]CACACCATCAACAGC | 219333 |
rs535479723 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27123226 | TGAGTCTGGTCTTGG[C/T]CATGACATTAAATTA | 219333 |
rs535504030 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27092382 | ATTCTAAAGTTTACA[C/T]GGAGAGGCAAAAGAC | 219333 |
rs535538259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27071747 | CTATGACTATGATTG[C/T]CCCTGCATCTCATTT | 219333 |
rs535540839 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153686 | TGCTGGATGTGAATT[G/T]AAGTCTCATTTCCCC | 219333 |
rs535543620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27115411 | GCACAGGGAATCACA[C/T]ACATCACTTCAACCG | 219333 |
rs535560022 | in-del | -/CAGGCTGAGA | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27075996 | ATCACGCCACTGCAC[-/CAGGCTGAGA]TCCAGCCTGGGTGAC | 219333 |
rs535564968 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27107392 | ATTGTAGCTATATCA[A/T]AGGACAAAGCAAACA | 219333 |
rs535608593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27115864 | TATACTTGTACATTT[A/G]TACCATTTAATCAAG | 219333 |
rs535617990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143322 | GGGTAGGGAGTATCA[C/T]ATTGATTCCTTATTC | 219333 |
rs535670006 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27113317 | CAAATAAAAAATAAA[A/G]ATGTTGAAAAGGAAC | 219333 |
rs535678495 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136366 | AGCCGGGCATGGTGG[C/T]GCATGCCTGTAATCC | 219333 |
rs535678847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143961 | ATAATCCCAGCACTT[C/T]GGGAGGCCAAGTTGG | 219333 |
rs535735966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27109391 | TTAATCAAGTCTCTA[C/T]GTGTAACTACTAATT | 219333 |
rs535798717 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142493 | TTTATGAAAGAGAAT[C/G]TCCCTGTTACTGGGA | 219333 |
rs535820977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156173 | AAACCAGAAGTACAC[A/C]TCACCTAAGTTTTTC | 219333 |
rs535830179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163244 | ATTTTAATGTGAATC[A/T]ATACTTGGTAAACTC | 219333 |
rs535831513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070226 | CATGCTATGTGAGTC[A/C]ATTTATATTCAAGCC | 219333 |
rs535862194 | snp | A/C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066694 | AGTTACAATAATTTA[A/C/T]AGAAATTTTTATTCC | 219333 |
rs535863870 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138505 | AAACACATGAGCAGC[C/T]TGACATGCCTCAGAC | 219333 |
rs535891771 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27103206 | GAAAGTCAGTGGAAA[C/T]ACTGAAATGAGTAAC | 219333 |
rs535905477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104008 | GAAAAGGGAAATAAT[G/T]TATGCTCTGTATGAG | 219333 |
rs536007896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140507 | GCACAATAACAATAG[C/T]GTAATAGTCTAGGTA | 219333 |
rs536023927 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148450 | GGAGGCCGAGGCGGG[C/T]AGATCACGAGGTCAG | 219333 |
rs536060462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27100540 | GATGGCCTGATTCAG[C/T]TTCTCTCTCCACTTT | 219333 |
rs536068860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141433 | TCTTGGTTTCTAAAT[A/G]CCATTCTCCACTAAA | 219333 |
rs536111245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27085461 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCATCT | 219333 |
rs536130068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132973 | GTGATGGCAACACAG[C/T]CATGCTCCTACTATG | 219333 |
rs536204721 | in-del | -/TAAGTA | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168513 | TTATTTCACACTTAT[-/TAAGTA]TAATATTAAATATCA | 219333 |
rs536237793 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167093 | ATGGAGAAACCCCAT[A/C]TCTACTAAAAATACA | 219333 |
rs536301512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27087673 | AAACCAGGGCTCCTT[A/G]GAGAAATGGCTTGTT | 219333 |
rs536391091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27088397 | ACTCCAGCCTGGGCG[A/G]CAGAGCGAGACTCCG | 219333 |
rs536426288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27072785 | AACAAACATTTGCTA[C/G]AAGTCTCTTCTAGGC | 219333 |
rs536429772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27080851 | TTATGTCTGAAAAAA[A/G]TCCATATCTTAATTT | 219333 |
rs536521429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27081810 | TTAATCTCTTTGTGC[A/G]TCTCCATCAGAGCTC | 219333 |
rs536610872 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142681 | ATTACAGTAGTCAGT[C/T]TGGAGGGGCTTCCAC | 219333 |
rs536665196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27095507 | CCTAAGAATTACAAC[A/T]TTCAAGTTCATCTTC | 219333 |
rs536734851 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139501 | TGCACCTGTGGTCCC[A/G]GCTACTCAGGAGGCT | 219333 |
rs536737869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27108325 | ACTCATAGATGGGAA[C/T]TGAACAATGAGAACA | 219333 |
rs536757245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27076494 | TCAGCACCTTACAGG[C/T]TCACTTTATATATGT | 219333 |
rs536853072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170436 | GAGGCATGAAACACA[A/G]GATTTCAGAAGTCTC | 219333 |
rs536860347 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136410 | GGCTGAAGCAGGAGA[A/G]TCGCTTGAACCGGGG | 219333 |
rs536879771 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070352 | AGGGGGCCTGCTGCG[G/T]TGTTGAAAATGAATT | 219333 |
rs536899904 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166964 | TGGGCATGAATGATG[A/G]TAATGATAACATGAT | 219333 |
rs536916983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073223 | CCCTGGGGTGGGGGC[A/G]GGATACCAAAGACCT | 219333 |
rs537060983 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171034 | TTCCGTCCTCTCCCA[C/G]GCGGGAATGAGCGCT | 219333 |
rs537064685 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125997 | CGGAGCCCACCACAG[C/G]TCAGCAAGGCCTACT | 219333 |
rs537071836 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135421 | AACGTTTAAGTATTG[C/G]GTCTATGGAGGCCGG | 219333 |
rs537100231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161174 | TCTTCATTAAGCAAA[C/T]TAAACAAACAGGGAA | 219333 |
rs537101304 | snp | C/T | | | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168954 | GCTGATTCTGAGAAG[C/T]GTTCTGTTTAAGTCC | 219333 |
rs537101932 | in-del | -/TAATA | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124491 | GTTTCCACACAACTT[-/TAATA]TAAATAAAGAGAAAA | 219333 |
rs537134639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136177 | TCAAGGCTCCTAAGT[C/G]CAAGTCTACAACAAG | 219333 |
rs537134750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127358 | TGGTACCAATGACAT[A/G]AAAGGGAACAGAGAG | 219333 |
rs537139963 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141910 | TGAAAGAGGCTGGGC[A/G]TGGTAGCTCATGCCT | 219333 |
rs537147677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119601 | AAAATTAAAAGATTA[A/T]GTGATTTCTAAAATC | 219333 |
rs537163634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162028 | AAATGACTACGCTTT[A/G]TCAAAGGTAACTTGT | 219333 |
rs537177065 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166721 | AAAAATTTCAGATCA[-/T]AACAAGTCTTATCTT | 219333 |
rs537187171 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27170093 | TTAGCCCAAACAATT[A/C]TCCAAAATCATTTTA | 219333 |
rs537387780 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27115079 | CTGTGGCCCCTGTAG[A/C]TATGTTAATTTTATA | 219333 |
rs537390801 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099267 | GTAAGAATGTATGCA[A/T]GTATTATTTGCATGC | 219333 |
rs537398765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27122422 | CAACTAAAACTCTTT[C/T]TCTTCACGGTCTTGG | 219333 |
rs537405244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125306 | TGAATAAAAATTAGC[A/T]TTTCATGATTACATA | 219333 |
rs537450756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27116028 | TTAAGATGTCAGGCA[A/G]CTGGCTGGGTGTGGT | 219333 |
rs537463377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119033 | AAATGTTAGCAACTA[A/C]TTTATAGGGTGACTA | 219333 |
rs537464700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122773 | TGTCAATGTAAGGTT[A/G]TTAATGAAAACTCAA | 219333 |
rs537539947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27111954 | ATAGGTGCAAGGGAA[A/T]GAGAGTCTCACTACC | 219333 |
rs537635694 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153261 | GCAGTGAGCCAAGAT[A/C]GTGCCACTGCACTCC | 219333 |
rs537660666 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27072714 | GGGAGAGAGGGATGG[A/G]AAATCACGAAATGGT | 219333 |
rs537689728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145834 | AGAGGTTACAAAATG[A/G]AAGAAAAGCAAAAAA | 219333 |
rs537699422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106431 | CGGGGAAATAAACCT[A/G]CTTTATAAAGTAAAT | 219333 |
rs537746897 | in-del | -/TGCAGCTGACAGCAGTCTAGC | 0.0861826 | 0.188849 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117438 | AGTATCATTTATGAT[-/TGCAGCTGACAGCAGTCTAGC]TGCAGCTGACAGCAG | 219333 |
rs537747043 | in-del | -/AA | 0.489024 | 0.0732638 | intron-variant | USP12 | GRCh38.p7 | 13:27084498 | AGAGACAGTGAGATG[-/AA]AAAAAAAAAAAAAAA | 219333 |
rs537753692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142321 | AGTCGATAAAGACGA[A/G]AAAAGGCGGAAGAAT | 219333 |
rs537757686 | in-del | -/A | 0.0256215 | 0.110247 | intron-variant | USP12 | GRCh38.p7 | 13:27093297 | TATGAACTAGTAGCC[-/A]AAATTATACCCGAAA | 219333 |
rs537759087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138673 | GGTTTCACTTCAAGA[C/T]GGTGTCACTCTTGCC | 219333 |
rs537799836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27087772 | GAGAATGACTGGGCA[C/T]ATCAAGAAGAGAGGA | 219333 |
rs537833512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156439 | ATATAGTGACGAAAC[A/G]CAACGATGATCATTA | 219333 |
rs537868694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27100132 | TGCATAGAACCTTGC[A/G]TGGTTCCACCAATTG | 219333 |
rs537893634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152033 | GATGCAGAGAAATGG[G/T]AACAGCCATACACTG | 219333 |
rs537933870 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27100779 | TTGGAAACCAACTGG[A/G]AAAGTCCTAGAGGAA | 219333 |
rs537952455 | in-del | -/AG | 0.00279162 | 0.0372561 | intron-variant | USP12 | GRCh38.p7 | 13:27078502 | GTATTCTAACATAAC[-/AG]GGGGTTGCCTTTCTT | 219333 |
rs538096042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27102954 | CTGTTGCTGTACTCT[A/G]TGCAGGAGCACTGTG | 219333 |
rs538120462 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27070735 | ATTTTGTATTTTTAG[A/G]AGAGACAGGGTTTCT | 219333 |
rs538191018 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27172078 | GGGAACTCCGGTCCG[C/T]CCCCACCCCGCGCGC | 219333 |
rs538221942 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27097167 | TCCCATAGTAAGTTT[-/A]AAAAAAAAAAAAAAG | 219333 |
rs538267654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104911 | AATGATTAAAATGCC[C/T]ACATTAAACAAAAGC | 219333 |
rs538269228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27097141 | GCTAAAAAACATGAG[A/T]AAATGTTCAATCCCA | 219333 |
rs538379275 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27103945 | ACATCATTGTATAAA[A/G]AGCCCATGTGATAGG | 219333 |
rs538402600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144826 | GCACTTTGGGAGGTC[A/G]AAACAGGCAGATCCT | 219333 |
rs538417069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27094544 | CCACCACCTTGACTG[A/G]GTGATCAAAAATTAA | 219333 |
rs538501291 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130219 | CTGGCAGTAGCCTGG[A/G]GAAACAGCACAGATT | 219333 |
rs538541377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126323 | AGCCTCTGCTGGTGA[C/T]ACCCAGGCAAACAGG | 219333 |
rs538620481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147821 | TGCCAATGCTTCCAT[C/T]TAAATGTGAAATAAA | 219333 |
rs538645488 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168319 | CTCCTACAACCCAAA[C/T]AGGAAGAGACAATAA | 219333 |
rs538683186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148471 | ACGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 219333 |
rs538721162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27080993 | GTGGTTGCTGAAGGT[C/T]GGGGTGGCTGAGGCA | 219333 |
rs538764194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27081613 | ATATTCTAATGGCAC[C/T]CAGAATGGTGAATCC | 219333 |
rs538810857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082725 | GTAAGGTTATTAATT[A/G]GCCTAATTTCAATAT | 219333 |
rs538842487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074020 | ATTCTTGCTGAGGAT[A/T]AAAGACGGGACCCAA | 219333 |
rs538854967 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066215 | GTGCCTTCTTCAAGA[A/G]CCTTAAATGCTTTAC | 219333 |
rs538880155 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066855 | TCTTCATGGGTCACT[C/T]TTCTTACTTACTATA | 219333 |
rs538987945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161013 | TCATCTTTCAAGGCC[A/G]TTAAGTCTGAAACCT | 219333 |
rs539010053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27088605 | GAGTCTGGAATTTGG[A/G]GGCATGGTAGGCAGA | 219333 |
rs539011414 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27079069 | GCCATAGGACAAACA[C/G]AACATCACAAGGGAA | 219333 |
rs539034856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136296 | TGAGGTCAGGAATTC[A/G]AGACCAGCCTGGCCA | 219333 |
rs539049125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27085400 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 219333 |
rs539127575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132052 | TAGCTAGATTTACCA[A/G]TTCTCATATAGCACG | 219333 |
rs539129392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123859 | GGACTAATACATAGG[C/T]AATGGGGCAAGTATC | 219333 |
rs539134562 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27077419 | ATGGCCCGATGGTTA[C/G]GGAAAATGTGCTTTT | 219333 |
rs539197683 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27111161 | TACTTTCATCAATCC[C/G]ATTAAAGAAAAATTA | 219333 |
rs539201066 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27081036 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 219333 |
rs539228599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118121 | CATATGGTCAACAAC[A/G]CACCAGTACTCAGAA | 219333 |
rs539237089 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146295 | TAGTCCCAGCTACTC[A/G]GGAGACTGAGGCAGG | 219333 |
rs539239700 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27079166 | TCCCTAGAGCAGACC[C/G]TGAGACAGAAAGTCC | 219333 |
rs539247248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27070842 | ACAGGCGTGAGCCAC[C/T]GCACCTGGCCTCCCT | 219333 |
rs539251410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164188 | GTACTCTAACTCTAC[C/T]GAAAGATATTATGAT | 219333 |
rs539281619 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160794 | TTCTTTTTTTTTTTT[C/T]TCCCCCTTCAACCTT | 219333 |
rs539313747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157544 | TTTTTTAAAAAAAAT[A/G]TAAGTTTATAGAAGA | 219333 |
rs539314330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27110933 | TCATCTCCAAGTATA[C/T]CAGAAATATTATGAT | 219333 |
rs539345788 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27108277 | TCTCAGGAAACTATC[A/G]CAAGGACAAAAAACC | 219333 |
rs539415675 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119646 | ATTCTATCGTTTCCG[A/T]TCACTTTCATGAATG | 219333 |
rs539450167 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27097759 | AATAGGTTTTGTATT[C/T]TGTTCAACAACAACC | 219333 |
rs539453493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136780 | ATAAAAAAAGGAAAA[C/T]CTAGATCAAACATAT | 219333 |
rs539505539 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155603 | TCCTGTGCCTAAGAA[A/T]TTGAAGTTGCTTTTG | 219333 |
rs539506924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162667 | TGTTAAAGAGATTGC[C/T]CTTTCATTTTAGGTA | 219333 |
rs539518925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27121141 | TGCATAAGGGAACCA[A/G]TAATAATCCCATACC | 219333 |
rs539536500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128528 | ACTGGCACCTTACCT[A/G]AGGCAAAAAGGGTGG | 219333 |
rs539538398 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068687 | TTGACCAATTGCTCC[C/T]TACATATACATATAC | 219333 |
rs539552043 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163453 | TCTAAGAAGCTTTTT[C/T]CTGAAGCCCTCTTCT | 219333 |
rs539576378 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155660 | AACCCTGAGGCGGAA[-/C]ATATTAAAAAATGGA | 219333 |
rs539610439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27121777 | GAAGCAGGAGAATGG[C/T]GCGAACCTGGGAGGC | 219333 |
rs539633322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150498 | GGAAGACTTTAACAC[G/T]TAAAATGGCAATACT | 219333 |
rs539638842 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130539 | TTCTCACACACACAC[-/A]AAAAAAAATCACAAA | 219333 |
rs539678364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164836 | ACTAGGAGATTGGGA[C/T]TGTAGGTTTTAGACA | 219333 |
rs539734752 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135215 | TCAATAGCTGAAGGC[A/G]GAGGTTGCAGTGAGC | 219333 |
rs539737919 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27115697 | TTTTCCCAAAGTTTT[A/C]AAAACGTGTAATTAC | 219333 |
rs539747034 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147431 | GATAATCTAAAAATT[C/G]TAGCTAACAAAGTTG | 219333 |
rs539751438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27108828 | CCGGGTGTGGTGGCA[C/T]GCACCTATAATCCCA | 219333 |
rs539774924 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172411 | TGTTTCTTTTTACGT[A/G]TATTGGATGAATCAC | 219333 |
rs539801791 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156393 | AAAGATAAACTATAA[C/T]AAAAAAGAAACAGGG | 219333 |
rs539811640 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27100891 | ATAATTCCCTACAGC[G/T]GCTAACTACATATTG | 219333 |
rs539815264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162093 | TTAATGTGCTTTCCA[C/T]CCTTTCCTTAAGAGG | 219333 |
rs539820854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152873 | CGTGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 219333 |
rs539826833 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113014 | TGAGGCAGGAGGATC[A/G/T]CTTGAGACCAGGGAT | 219333 |
rs539838335 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27120455 | ATCAGGAGTTCGAGA[A/C]CAGCCTGGCCAACAT | 219333 |
rs539840176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27076096 | GACAATTCCTTTGGA[C/T]TTGGGTAGACTGAAA | 219333 |
rs539840224 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068999 | ATAAAGAGAAAATGC[A/G]TGCCAATGACTGGAA | 219333 |
rs539876994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27069547 | AATGTTTATAAATAC[C/T]TATCTTCTAAAGCTG | 219333 |
rs539914186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106118 | CAAAAATTCTTTGGA[A/T]ATCACAAAAGTAAAG | 219333 |
rs539953809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138103 | AGCACACTGAGTACA[C/G]CCTTGCAGAGGGCAC | 219333 |
rs540016740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129921 | CATGAAAAATGGCAG[A/G]GTAGAAAGCTCCCAG | 219333 |
rs540024501 | snp | A/C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27113889 | AGACATTTGCCTAAT[A/C/G]AACTTTATAACCCAA | 219333 |
rs540098199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099922 | CCTACATGGACTTAA[C/T]AACTAATCTTGAATT | 219333 |
rs540165611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166522 | TGCAACTGGCCAACA[C/T]GGATCATGGTAGGGC | 219333 |
rs540169433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131166 | CAGTCAATATGGGAA[C/T]TTGAGTGTGGGTACA | 219333 |
rs540174750 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27084750 | TTCCACTGGTCTATA[G/T]ATGTCTTTAGGCCAG | 219333 |
rs540191227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109139 | GTTTCTGTTTATAAA[A/G]TAAGTCCAGTGAATA | 219333 |
rs540216029 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152669 | GAATATGTGCCGGGC[A/G]TGGTGGCTCCCGCTT | 219333 |
rs540224670 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27102042 | GAATGAATGAATGAA[A/T]GGACAATAGGGATTG | 219333 |
rs540253095 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136572 | CTTCTTCAATGGAGA[A/G]AATAGATAGGTAATT | 219333 |
rs540319369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27094758 | CAAAAAAAAAAAGAC[C/G]ATGTAAATGTTTCAG | 219333 |
rs540343076 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27121431 | AATGAGACAAATTCA[A/G]TCCACCCACGAAGAA | 219333 |
rs540361271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27087314 | GCATGCAGGGAGCGG[A/G]GGCAGGAAGGCAGAG | 219333 |
rs540370060 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27072135 | ATGGAGGATGACACA[A/T]CAAAACTTTTTCTTA | 219333 |
rs540400842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27122050 | AACTCAATGGTGTGG[C/T]CAGGCATGGTGGCTC | 219333 |
rs540407644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138851 | ATACAACAGAGAAAC[C/T]CATATTCACCCTGTA | 219333 |
rs540429936 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151362 | TTAGACTTCATCAAA[A/G]TCAAAATTAAATTTT | 219333 |
rs540464972 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | USP12 | GRCh38.p7 | 13:27115541 | TTTTATCAATATATG[A/C]ATTTTAAAACACCTG | 219333 |
rs540469522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130687 | ATCAATCGTATCAAC[A/G]GTATCACACTGGGGT | 219333 |
rs540503443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27116077 | CAGCACTTTAGGAGG[C/T]TGAGGTTGGCGGATC | 219333 |
rs540523210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157763 | ACCAAGCTTCCCTCC[C/T]CACCACTCCCAAAAG | 219333 |
rs540545651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27108585 | TGGGATATCTTAAAT[A/G]TAAGTGTCAACTTTA | 219333 |
rs540674816 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27086520 | GATTTACATTTATCC[A/G]TATTTTCTAATTTAA | 219333 |
rs540695800 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133397 | TATCATCTAAATTAC[A/G]TAAAAAGCTTTGCTA | 219333 |
rs540698193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170892 | GAGCTCGTGCCTCTC[A/T]GAGGAGAAAATGGAG | 219333 |
rs540730933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128857 | CACCTATGTTACAGT[A/T]TAATAAAGTATCTGT | 219333 |
rs540739773 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160495 | AAGTGAACTGTCTTT[-/A]AAAAAAAAAAAAATG | 219333 |
rs540756203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125443 | CAACACTGAGTGCTG[A/G]AGAACTTGGAAAGGC | 219333 |
rs540769453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070597 | TCACTCTTATTGCCC[A/G]GGCTGGAGTGCAATG | 219333 |
rs540803309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119286 | TAGTTTGGCAGACAA[A/G]AGCCAATTCCATGAA | 219333 |
rs540805970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27071317 | AGATAAAGCTACACT[A/G]AGTTGAACTGGTCAT | 219333 |
rs540811067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074864 | CATACGCAATTAAAC[C/T]CAGAAGTGATTTATT | 219333 |
rs540838370 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27112215 | CTACCTCTTAGAATT[G/T]CTTAAATAATTAAAT | 219333 |
rs540846268 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27080228 | CCAGAAGACTTGCAT[-/G]GGGGTGTGTGTGCCA | 219333 |
rs540903511 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113157 | GGAGGACGGCTTGAG[A/C]CAAGAAGGTGAAGCT | 219333 |
rs540968047 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27121860 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAATTAA | 219333 |
rs540986755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155656 | ATATAACCCTGAGGC[A/G]GAACATATTAAAAAA | 219333 |
rs541039534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082182 | AGACTGTTTCCTCTA[C/T]ATTGAAAATCTGTTG | 219333 |
rs541058667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159443 | AGGCATATAATTCTG[A/G]TGTTTTACAAGTGTT | 219333 |
rs541074398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074274 | GCGTGGTGGTGGGTG[A/C]CTGTAGTCTCAGCTA | 219333 |
rs541074505 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27097849 | GACCAGCAGTGGTTG[A/G]GACTTCAGACTGCTT | 219333 |
rs541091657 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066313 | AGGGAGACTGAAGCA[C/G]AGAGAGGTTAAGTGA | 219333 |
rs541092450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168104 | AGAAGAAAAGCCCGT[G/T]GGACTCTCCTAGCAC | 219333 |
rs541105491 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27109774 | CAAAAACTAGCCGGG[C/T]GTTTTACTCCTGTAA | 219333 |
rs541207876 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143176 | CAAAATCGAGAATAA[G/T]TTTAACATCATCAAA | 219333 |
rs541210431 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27111957 | GGTGCAAGGGAATGA[A/G]AGTCTCACTACCTAC | 219333 |
rs541238759 | in-del | -/TG | | | intron-variant | USP12 | GRCh38.p7 | 13:27108956 | AAAAAAAGATACATA[-/TG]TGTGTGTGTGTGTGT | 219333 |
rs541244651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154857 | AAGCAGGACAGTCGC[C/T]GTCCGAGGGAGGTAA | 219333 |
rs541266395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104225 | TTTGTGAGACAAGGT[C/G]TTGCTTTGCTGCTGA | 219333 |
rs541282407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162174 | TTATAGTACAAAGGA[C/T]GTTCACATGTGTCAT | 219333 |
rs541285455 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069099 | TGATACCTGAGCAAA[C/T]AAATCAACTACCATG | 219333 |
rs541294840 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167569 | GCTTAAGAAGCTTAA[C/G]TTTTGTTCCCTTCTT | 219333 |
rs541314975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27097396 | CTTGAACCCGGGAGG[C/T]AGAGGTTGCAGTGAG | 219333 |
rs541316591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27105398 | TATGAAAACAAATGC[A/G]TAAGCATGCAAAAAA | 219333 |
rs541355356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27089662 | TGATGATTAAATAAT[A/C]GCTAGACATAGGAAA | 219333 |
rs541387593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116890 | AGCCTAGGTGTGCAG[C/T]AGGCTCTACCACCTA | 219333 |
rs541411915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123943 | ACACCCAGAAATCAC[C/T]ATCCAAGTGAAATAA | 219333 |
rs541414790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163506 | TTCACATATAATTAC[C/T]ATTACTTATACCAAT | 219333 |
rs541472231 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160001 | AGTAAAAACCTGAAA[C/G]AGCGGAATTGCGAAC | 219333 |
rs541472353 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27114841 | AATTTTTTAAAAATT[A/T]GACAGGCATGGTGGT | 219333 |
rs541473330 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141126 | GTTCAAGCAATTCTT[C/T]TGCCCCAGCCTCCCG | 219333 |
rs541475711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117672 | AATGTATATTAAATA[C/T]ACTATATACCTGAGT | 219333 |
rs541490809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27110644 | GGTATGTGATTAAAG[C/T]GTACTGATATCAATG | 219333 |
rs541531293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154273 | TATTTTACATATACT[C/T]TGTTGAGCAAGGGCA | 219333 |
rs541578770 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27103574 | CTGCCTAAATACAAA[A/C]AGAATTAGTAACTAT | 219333 |
rs541595755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27100282 | CCTCTACTACTCTCA[C/T]TTGCTTATTGCACCT | 219333 |
rs541604195 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27111036 | ATTTTGTAGACTACT[C/G]GAAGTCAGGCTCACA | 219333 |
rs541679449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27093259 | CGGACTGGGAGAAAA[C/T]ATTTGCCAAAGACCC | 219333 |
rs541684565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147951 | TAGGCAACACAGGGG[A/G]ACACCATCTCTACAA | 219333 |
rs541749797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140827 | TGACAATTATGTCCA[A/T]GTCAGCTGACAATGA | 219333 |
rs541823739 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27106212 | AAGATCCCCTGAAAC[A/G]TTACATGAAAAAGTC | 219333 |
rs541834085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149718 | CTACAGCAACAGTCC[C/T]CAACCTTTTCGGCAT | 219333 |
rs541858361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27114427 | GTAAGTGGGATACTT[A/T]ACAGCAAAAGAAAGC | 219333 |
rs541915846 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27080343 | ACTGGAACTGGCTAC[A/T]GGGGAATAAGATATG | 219333 |
rs541920605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142787 | ATAAATAAAAATCTA[C/T]CGTGACACAAAAAAG | 219333 |
rs541923023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157636 | ACATTAAATCATGTA[A/C]GTAATTTTAATCACT | 219333 |
rs541969466 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27118908 | CATATGTACCACATA[C/T]TTTCATGCCTGCTTA | 219333 |
rs541981112 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27108315 | GCATGTTCTTACTCA[C/T]AGATGGGAATTGAAC | 219333 |
rs541984177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135571 | TCCAAAAAACTTAGC[C/G]GGGCATGGCAGCACA | 219333 |
rs541993805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142329 | AAGACGAAAAAAGGC[A/G]GAAGAATAATGATGA | 219333 |
rs542004549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27115315 | GAGTAATGAGTAGCC[C/T]GTTCTGGAGAGAGAG | 219333 |
rs542029645 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27085100 | CAAGTCTTCTGCCAT[A/G]TAAGTTTATTCCTAA | 219333 |
rs542056197 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128524 | GTAACTGGCACCTTA[-/G]CCTAAGGCAAAAAGG | 219333 |
rs542066353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27093938 | ATCCAAACAGGCTGC[A/C]TACTATATGATTTCA | 219333 |
rs542085427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127564 | CAATATAATTTTGCC[A/G]TCCAGTAGTGTTTAT | 219333 |
rs542143079 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170605 | GGCCACGCACAAAAC[A/C]CCAAGTTTTAAACGC | 219333 |
rs542143609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27120415 | CCCAACACTTTGAGA[C/T]GATGAGGCAGGTGGA | 219333 |
rs542144870 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163033 | ACAAGTTTTAACAAC[C/T]CACTGAACTGTCCTT | 219333 |
rs542150447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137175 | TATATTCCCTCAATT[C/T]CTTCATTTTGAACAA | 219333 |
rs542200782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27069941 | AACAAGACTGTCTCC[C/T]AAAACAACAAAAAGG | 219333 |
rs542256606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138976 | TTTCAACGGTAAGGT[A/G]TATGATCATTCAGCC | 219333 |
rs542257580 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27088654 | CCCCAAATAAAAACT[C/G]AGGGCACTCAGTCTG | 219333 |
rs542269668 | in-del | -/CTAG | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27090720 | TAGACATAAATCTTC[-/CTAG]CTATTTCCTTCAGCA | 219333 |
rs542280206 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27077211 | AATATAATTCAACTA[C/T]GAAACATCAGACCTT | 219333 |
rs542298246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099421 | GAACTCCTAGGCTCA[A/G]GCAATCTGCCTGTCT | 219333 |
rs542300639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147036 | GGCAGATCCTTCTCC[A/G]GCACCTTCAGAGAGG | 219333 |
rs542308427 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27110774 | TCTGTCTTTAAAATT[G/T]TATTTGTACTACAAT | 219333 |
rs542320131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139776 | ACTCACCTAGACTGA[C/T]TCACATATTTATTTT | 219333 |
rs542362919 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131048 | AATGACACTCAAAGT[G/T]TATGTGTGGCATTTT | 219333 |
rs542370974 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | USP12 | GRCh38.p7 | 13:27092198 | AAGAACTACCAAACT[C/T]CAATGAAAGATAGCA | 219333 |
rs542379487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131329 | TCTGGGTGAGTCACT[C/T]TCTCAGTCTTAGTTT | 219333 |
rs542398093 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128352 | TAACATCAAAAGGAA[A/G]ATTCTCAAATATGAC | 219333 |
rs542487640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157282 | AAGTTTTACATACAT[C/T]AAGCTAAAAAACAGA | 219333 |
rs542498399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128076 | TGGCTAAATGTGTTA[C/T]AGAGAATATTTAGAG | 219333 |
rs542519037 | snp | A/G | | | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169338 | AGGATACGGGGTGTG[A/G]CAGGGAGGAGCGTTC | 219333 |
rs542548583 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124747 | GTGAATGTGAGCTGT[A/T]AAAAGATGAATCCAA | 219333 |
rs542549063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160070 | CAGTCTTTAAAGAAC[A/G]AAAATACCACCTTAA | 219333 |
rs542564932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074122 | ATTCTCATCAGAGGC[C/T]GGGCGCGGTGGCTCA | 219333 |
rs542586951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146282 | TGGTGGGCATCTATA[A/G]TCCCAGCTACTCGGG | 219333 |
rs542594565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27078970 | GATAAATTTCAAAGA[C/T]GAAATCAGAGTATGT | 219333 |
rs542608276 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150200 | AAATATCACACTGTA[-/C]CCCCACAAATACATA | 219333 |
rs542629237 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | USP12 | GRCh38.p7 | 13:27087280 | GTGTGTGTGTGTGTG[C/T]GTGCGCGCACGCTCG | 219333 |
rs542631704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27095976 | ACAAATAACTTTCGC[A/C]TCTAAAACTTTTATC | 219333 |
rs542639014 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129727 | ATAAATGTATGCATA[A/C]TTTTTGTGAAGGATG | 219333 |
rs542667276 | snp | C/G | 2.48352e-05 | 0.00352377 | missense, upstream-variant-2KB, utr-variant-5-prime | USP12, USP12-AS2 | GRCh38.p7 | 13:27171599 | CCACCTACCATGGTA[C/G]AGATGGAGGCGAATT | 219333 |
rs542681907 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161481 | CAGGGATCCCTGAAA[A/C]ACCCAGGTAGACCAA | 219333 |
rs542702281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27088147 | TGCTTGCGGCCGGGC[A/G]CAGTGGCTCACGCCT | 219333 |
rs542784685 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27116204 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 219333 |
rs542790465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27080642 | TACTGTCACTAATCA[C/T]TGGATCCCACAGAGT | 219333 |
rs542823430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109307 | CAAGTGAACAACTGA[A/C]TATTGTGTGTCTTTT | 219333 |
rs542823445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116790 | TATGTTCAGATGCAC[A/G]CTTATTCCTGTGTTA | 219333 |
rs542836414 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123977 | TAGGTTGAAATTACA[A/C]AGATACCTTTGACCT | 219333 |
rs542891327 | snp | A/G | 0.000106455 | 0.00729493 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117760 | AAATTCAAGAAACAA[A/G]GACCTCGCACAGACA | 219333 |
rs542951029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27102166 | ACTACAGATGCCAGC[G/T]GATGTGGCCCTCAGG | 219333 |
rs542999112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074961 | CTAGGAAATCAGATA[C/T]AGTACTTGTAGAGTA | 219333 |
rs543007068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137879 | GGAGCAAGCTGCCGC[A/G]CTGAGAGGACTTATG | 219333 |
rs543015502 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27081998 | CAGGGTAGATTCAGC[A/G]TAATTCTTAAGAACT | 219333 |
rs543071118 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172506 | ATTACACATGTTTAA[C/G]TCTTTGAATTAAGAA | 219333 |
rs543085257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27075796 | ACACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 219333 |
rs543097862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27122474 | GGAAACGGACTAATA[C/T]ACCCCATCTTTACCG | 219333 |
rs543123574 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169464 | ATAAGACTGCAAATT[A/T]CTTTGAGATATTCAG | 219333 |
rs543138013 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27106048 | GATGACAATCGGTTA[C/G]TACTGTTACTATAAC | 219333 |
rs543151037 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27072331 | GGGTGGGGTAAGGAC[A/T]GGTAAATTGAAAAAA | 219333 |
rs543161729 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069133 | GGAAGGGCTTGTCAA[C/T]CCATCGTCTTTGCTT | 219333 |
rs543169551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165472 | CCAATGAATACTTTT[C/T]ACCACAGGGAGGGGA | 219333 |
rs543220005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106337 | TTACCAGCCATGTCA[C/T]TGGGGTATGTCACTA | 219333 |
rs543221276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27113170 | AGCCAAGAAGGTGAA[A/G]CTGCAGTGAGCCAGG | 219333 |
rs543228315 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102479 | TGGCTTTCCAAATAA[A/T]ACCCAAGCTTTAGGC | 219333 |
rs543230862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166345 | GCTTAAAAGATACTT[C/G]CTGAGACAATAAAAG | 219333 |
rs543262594 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27092739 | AGGATCATAGACTTA[A/G]ATATAAAATGAAAAA | 219333 |
rs543307328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106757 | TAACAAAAATGTTTA[C/T]AGGAGAAGAGGAAAA | 219333 |
rs543342708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27102539 | ATTCCACTCTTGCCA[C/T]GCTAATTTTCTTTCC | 219333 |
rs543372483 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150784 | TGGTTTTCAACAAGA[C/G]TGCCAACTCCAAAAG | 219333 |
rs543373810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125528 | TCCGGTCTACAGCTC[A/C]CTGCGAGATCGATGC | 219333 |
rs543390788 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159772 | GGAAAGCTAAAATTA[C/G]AGATGTCACATTCAA | 219333 |
rs543409751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160878 | TCATGGTGGTTTGCT[C/G]CACAGCTCAACCCAT | 219333 |
rs543414945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168963 | GAGAAGTGTTCTGTT[C/T]AAGTCCAGCCCATCT | 219333 |
rs543424526 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117580 | ACACAATGTTAAATG[-/A]AAAAAAAGAAAAATT | 219333 |
rs543471696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126748 | ATAGCAGCACTACTG[C/T]AGAGTTACCAAAGTT | 219333 |
rs543475618 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068637 | ATTATAATTACAAAG[C/G]CAGTCTTTCCCCTTG | 219333 |
rs543525637 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155281 | AGAGACAGGGTTTCA[C/T]CATGTTGGCCAAGAT | 219333 |
rs543594698 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141065 | TCTGTCACCAGGCTG[C/G]AGCGCAGTGGCACAA | 219333 |
rs543632993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148752 | CTAACATAAAATAGC[A/G]TATCAATTGAATTAA | 219333 |
rs543635018 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165749 | TAGGCTGTTGGTGAC[A/G]AAAATGGTGGTATCA | 219333 |
rs543639736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155812 | ATTAAGTCTAGATGC[A/G]GAAAAGGTTCAACTT | 219333 |
rs543695975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27098852 | GCAACGGTTAAAATG[A/G]AAACAGTTCCATTGA | 219333 |
rs543700636 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141798 | AAAATCTGAACTCCA[A/G]AATGTTCCAAAATCT | 219333 |
rs543809419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27110732 | CTGAATGTTACTAAG[A/G]TTAATTTACCCAGTA | 219333 |
rs543850457 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142953 | CAAAAATTAACTGGG[C/T]GTGGTGCCACACGCC | 219333 |
rs543858735 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154972 | CAAAGGCAAAGAAAC[A/C]GTCCCTCCTGCAGCT | 219333 |
rs543871472 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147169 | AAAGACCCTAGGAAA[C/T]GAATACACCATGGTA | 219333 |
rs543925872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152831 | CCTGTAGTCCCAGCT[A/G]CTCAGGAGGCTGAGG | 219333 |
rs543926926 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27097408 | AGGTAGAGGTTGCAG[G/T]GAGCCGAGATTGCGC | 219333 |
rs543934715 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167155 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 219333 |
rs543993094 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144340 | CCTCTACAGAAAAAT[A/T]AAGTATTAGCCAGGC | 219333 |
rs544010652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140923 | TCTCTCTAACGCCTT[A/T]TGTAGCTATTCCAAT | 219333 |
rs544011131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27094070 | GCACAACTGTCACAG[A/T]AAAGATGAGATCAGG | 219333 |
rs544013738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27089786 | ATTAAGAATTTTTAC[C/T]CAATGTAAATTTTCC | 219333 |
rs544097629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27086780 | CTTATCCAACGGTCT[G/T]AGGTACTTTCTAAGG | 219333 |
rs544138173 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP12 | GRCh38.p7 | 13:27075944 | CTGGGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 219333 |
rs544147832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27079656 | CTCAATAGTCAGAAA[C/T]GTTTTTTAAAGTAAA | 219333 |
rs544164986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27115471 | AATATGTCCTATGTA[A/G]GGACTAATATTTAGA | 219333 |
rs544234569 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27108452 | GAGGAGTTAATGGGT[A/G]CAGCACACCAGCATG | 219333 |
rs544240399 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124751 | ATGTGAGCTGTAAAA[A/G]GATGAATCCAAAGTA | 219333 |
rs544274486 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27122151 | ACATGGCGAAACCCC[A/G]TGATATGGTTTGGCT | 219333 |
rs544305579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127744 | CCACAGAAGCACATA[C/T]GTAACATATTAAACA | 219333 |
rs544319347 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27100840 | GTAAAAAGATTTTAT[A/T]AACACTGCTGAGGAC | 219333 |
rs544480034 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27073823 | AAGAGAAAACTGAAG[A/G]CTTTTCAGGAAGCTA | 219333 |
rs544490135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170691 | AGTCTATTTAAACGC[C/T]CTAGGAAAACAAATA | 219333 |
rs544523057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27121389 | CTCTTCCACTCCACA[A/G]AAGGCAGAATTACAA | 219333 |
rs544540941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157237 | CAATAAATTTTCTAG[A/G]AAACCACTTCTGATC | 219333 |
rs544551764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163701 | TCATCCCAGCACCTT[A/G]GGAGGCCAAGGCAGG | 219333 |
rs544656413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27093104 | GGGAGGCTGACACAA[A/G]AGAACCACTTGAACC | 219333 |
rs544712700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132501 | TAAATTACTGCCCCT[C/T]GAAGGAGACTCTTCC | 219333 |
rs544723427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140649 | ACTGAAGTCTTCTCT[G/T]TAAGTCAGCACTTCA | 219333 |
rs544737735 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27089562 | GGCAATGGGGAGTGC[A/T]ATCTCCCTCAACCCT | 219333 |
rs544740413 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27085481 | CCACCGCATCTGGCC[A/G]TCAAATTGATTTTTG | 219333 |
rs544745803 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156593 | GAAGCCAAGACAGGC[A/G]GATCACCTGAGGTCA | 219333 |
rs544764372 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27076865 | TGGCCTTTTGGAAAC[A/T]TTAGCCAAAGTAAAG | 219333 |
rs544806048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27078025 | TAAACACTGATTTTT[A/T]AAAAATCTTCTGTAA | 219333 |
rs544862303 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171303 | GGGGACTCCCGGAGG[A/C]CGGTGCCCGCCCGAC | 219333 |
rs544884123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119185 | TAATACATCTTTTCT[A/G]CTCCGTGCAAAAGCT | 219333 |
rs544945858 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27096716 | CCACCATGCCACACA[C/T]AAAGTAATGCCCAGT | 219333 |
rs544946207 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168685 | TACTCACTGCAATCT[A/C]AACATAATCACTCAT | 219333 |
rs544970073 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127099 | TTCCTCCTCTAGTGG[A/C]CTCCTCTATGTTAAA | 219333 |
rs544987862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27072401 | GAACAGTAGACAAAA[A/G]TTAATTTCATAAACT | 219333 |
rs544988238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27080434 | CAATCATTAAATCTA[C/G]GGCAGATACTCAGAG | 219333 |
rs545048557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27081438 | CAGTCAGATCGTCAG[G/T]ATCCTCTTCTAATTC | 219333 |
rs545082949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165588 | ATGTTATTTTACTCT[A/C]ACTTTACAGGTACAG | 219333 |
rs545114950 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27116248 | ACCCGGGAGGCAGAC[A/G]TTGCAGTGAGCCGAG | 219333 |
rs545131659 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124843 | ACCCTCATACCTGTT[A/C]TAGAAAACACCATGT | 219333 |
rs545180855 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162035 | TACGCTTTGTCAAAG[A/G]TAACTTGTGAGCTCC | 219333 |
rs545201616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27102754 | TCGTGACAGTGACAC[A/G]TTACATCACACAATT | 219333 |
rs545291885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27103354 | CAAAAGCCAAAAATA[C/T]ATTTCAAAACATATT | 219333 |
rs545298202 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067123 | TAACTTGGCTTTTAC[A/G]GCATGTTTTTTTTTA | 219333 |
rs545328763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27096636 | ACATGAAAATGGGAC[A/G]AGACAGAGTACAGTC | 219333 |
rs545379092 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137773 | AGAAAATGACGGAAG[A/G]GATGGGATGTCACTT | 219333 |
rs545390468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122590 | CTGGGAAGTGGAAGC[G/T]GCAGTGAGCCGGGAG | 219333 |
rs545401749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27170146 | GCTTTCCTAAAATGT[A/C]AACTGTGAGAAAGAA | 219333 |
rs545465398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116819 | TACGATTGCCTAGAA[A/G]ATACAGGAACATGCT | 219333 |
rs545466999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27069835 | GCCTGTAATCCCAGC[C/T]ACTCGGGAGGCTGAG | 219333 |
rs545488895 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160005 | AAAACCTGAAAGAGC[A/G]GAATTGCGAACACTT | 219333 |
rs545550892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109742 | AACATGGTGAAACCC[C/G]GTCTCTACTAAAAAT | 219333 |
rs545551189 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163030 | TTAACAAGTTTTAAC[A/T]ACCCACTGAACTGTC | 219333 |
rs545559480 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113510 | CCCACCACGCTTCTT[A/T]CTCCAGCAGAGTAGA | 219333 |
rs545606737 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27104321 | TAGGTGTGAGCCACC[A/G]TGTCCAGTCACTGAA | 219333 |
rs545680603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27092480 | TTACTCTAAAGCTAC[A/G]GTAATCAAGACAGTG | 219333 |
rs545707619 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076761 | GAAAAAAAAAATCAT[G/T]TTATAACATTATACT | 219333 |
rs545735210 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139877 | TTATCCTTACAGAAA[A/G]GGAAACAGAGTTTCT | 219333 |
rs545760038 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27074278 | GGTGGTGGGTGCCTG[C/T]AGTCTCAGCTACTCG | 219333 |
rs545768812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119880 | CCTGTGGTAATGACA[C/T]TGCGCAGCAGATTCT | 219333 |
rs545769598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27076608 | CCTTCATTTTTATTT[C/T]CCCACTATCTAGCAA | 219333 |
rs545787263 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127439 | GAGAAATGAAATATT[A/G]TACAACCAGTTATCA | 219333 |
rs545795630 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173481 | CTTGTCCATTAATCC[A/G]AACATGTCACAGGAA | 219333 |
rs545796907 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27107468 | GGAAAAAAAGATGCT[A/G]TAATAAAAATCAGAA | 219333 |
rs545822801 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP12 | GRCh38.p7 | 13:27113190 | AGTGAGCCAGGGAGG[C/T]GAAACTGCAGTGAGC | 219333 |
rs545933417 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27112635 | ACTAAAATTCAATCA[C/T]ATAATTCTCTAAAAC | 219333 |
rs545983740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27107641 | TCTCCTATACCCAGA[C/T]TGTGTTCTCTAAACA | 219333 |
rs545997013 | in-del | -/TTTC | 0.00301507 | 0.0387097 | intron-variant | USP12 | GRCh38.p7 | 13:27085164 | ATGTTTTCTTTTTTC[-/TTTC]TTTCTTTCTTTCTTT | 219333 |
rs546017809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150961 | AAAACTCTTAAACAC[A/T]GGATTTGGCAAAGGA | 219333 |
rs546080553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151377 | ATCAAAATTAAATTT[G/T]GTGCTTCAAATGGCA | 219333 |
rs546080636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142887 | ATCACGAGGTCAGGA[A/G]ATCGAGACCATCCTG | 219333 |
rs546097009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154347 | CATGCTACCAAGCCT[A/G]TATTTACTTACTTAT | 219333 |
rs546147315 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27085470 | ACAGGCGTGAGCCAC[C/T]GCATCTGGCCGTCAA | 219333 |
rs546147410 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27113820 | AACCTATGGCCATCA[A/G]ATGAGGAGAAACTGA | 219333 |
rs546166231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144525 | AAAAAAAAAAAGGTG[A/G]TAGGTCAACTTGAGA | 219333 |
rs546180717 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27081492 | CATCTACAGTGACTT[C/T]CTCCACTGAAGTTCG | 219333 |
rs546188342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104678 | TTCAAGAATAATAGC[C/T]TATAGCCTATTTCTG | 219333 |
rs546223107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27105305 | GTTTTGATTTTTCAC[A/G]GCTAAAATGGGGGAA | 219333 |
rs546232427 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27078803 | ACTTCTCTCACTAAC[-/A]AAAAAAAATCAGTAA | 219333 |
rs546237502 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076837 | TCCTAAATTACTTAC[C/T]AGTGAATGAACTTGG | 219333 |
rs546254211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136803 | AAACATATTAAAAAG[A/G]TAAAAATACAATATT | 219333 |
rs546284893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27085983 | TGAGCCTAGGCAACA[C/T]AGCAAGAGCCCGTCT | 219333 |
rs546317617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128532 | GCACCTTACCTAAGG[C/T]AAAAAGGGTGGGCAA | 219333 |
rs546368826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27078415 | GAGGGTCCTGGAACC[A/G]ACTGATACGGAGCAT | 219333 |
rs546387472 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149721 | CAGCAACAGTCCCCA[A/G]CCTTTTCGGCATCAG | 219333 |
rs546393772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27083003 | ACCACGTCCAGCTAA[C/T]TTTGTATTTTTAGTA | 219333 |
rs546404703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27071614 | CTTGAAACAGGCAAG[G/T]ATATCAAATCCTTGG | 219333 |
rs546435561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27091295 | GTAAGCTACAGAGAA[A/G]TAAAAGTTACACAGT | 219333 |
rs546529593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126836 | AAAAGGGCAAACAAG[A/C]CTTGCAACATGGCTT | 219333 |
rs546561262 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27089185 | TATAAAGGACATTAC[C/T]GGTACATCCTGTGAT | 219333 |
rs546565001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27108919 | GTACTCGGGCTTGGG[C/T]GACAGAATGAGACTT | 219333 |
rs546578087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27119984 | TCTCTCTAGCCTAAC[A/G]CTAACTAAAAAGGCA | 219333 |
rs546586950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27093568 | ACTCTCATTCACTGC[C/T]GGTAAGAAGGAAAAA | 219333 |
rs546615120 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27120579 | GTGAGTCAAGATTGC[A/G]CCACTGCACTCCAGC | 219333 |
rs546623841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27094281 | GGCTGAGGCAGGTGG[A/G]TTACTTGAGGGCAGG | 219333 |
rs546639335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152584 | CTAAAAGCCACTAAA[C/T]TGTACACTTTAAATG | 219333 |
rs546647398 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27116108 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 219333 |
rs546674139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129276 | CTGTTTTCTAGACCT[C/T]GATTCCCCTGACCTA | 219333 |
rs546729849 | snp | A/C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146951 | AAGATGTGAAGAGAC[A/C/T]CAGGGAAAAGAGGGC | 219333 |
rs546740287 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27114861 | GGCATGGTGGTGTGT[A/G]CCTGTGGTCCCAGCT | 219333 |
rs546778311 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151208 | TGGTAGCGCGCAATT[C/G]TAATCCCAGCTACTC | 219333 |
rs546792184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113776 | GATATGGATATTTTC[C/T]GGACTCTCCAACAAT | 219333 |
rs546830899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27107357 | AAAAACAAATTTATT[A/G]ATATTGTTATTTTGA | 219333 |
rs546852898 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | USP12 | GRCh38.p7 | 13:27088622 | GCATGGTAGGCAGAG[G/T]GTACCTACATGACTA | 219333 |
rs546866516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27115723 | ATTACTAGAATTACC[A/T]CCATAAGAACTGGGA | 219333 |
rs546899643 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158729 | CACTTTGTTATGGCA[G/T]CCCTAGGAAACTAAT | 219333 |
rs546903330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27116434 | AAAAGAACAATTTTC[C/T]TTTAATAACTTATGG | 219333 |
rs546949860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117299 | TAATCTGATAGCACA[C/T]ATCTCTCAGAGCTGA | 219333 |
rs546987500 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27077035 | ATTAGAGTTCTTTTA[A/C]ATTGTAAAAAATCCC | 219333 |
rs547020586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170398 | ATCTCCTATATGAAA[A/T]CAGTTGCATAAATAG | 219333 |
rs547032404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27069572 | AAGCTGAACATACAA[C/G]TACCCTTTGATCCAG | 219333 |
rs547096305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073829 | AAACTGAAGGCTTTT[C/T]AGGAAGCTATGCATA | 219333 |
rs547099222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163765 | ATAGAGCAAGACCTG[A/T]CTTAAAAAAAAAAAA | 219333 |
rs547181977 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147773 | AAAGGAAAAAAAAAA[A/T]TTTAAAAAACCGTCA | 219333 |
rs547201243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160929 | ATCCATCAGCTCTTC[C/T]TCCTGATGCTCTCCC | 219333 |
rs547212846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27107977 | GAAGTCAGTGTGGTG[A/G]TTCCTCAGGGATCTA | 219333 |
rs547245171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148438 | GCCAGCACTTTGGGA[A/G]GCCGAGGCGGGCAGA | 219333 |
rs547254766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099973 | TTTGTCCACAAGAGA[C/T]AGTAGATCTAAAGCA | 219333 |
rs547264472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155156 | GCGCGATCTCGGCTC[A/G]TTGCAACCTCCGCCT | 219333 |
rs547284452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104776 | ACTGACTAATTTAAA[A/G]GCAGGATTACGCAAT | 219333 |
rs547300640 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159430 | TTCCATTTGCATCAG[A/G]CATATAATTCTGGTG | 219333 |
rs547311367 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130780 | CTTGTTGAAATCTCA[A/G]ATTTCCTGGATGAGA | 219333 |
rs547372076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27097622 | ACTTCTAACTGCACG[C/T]GTGGCATAGGCAACT | 219333 |
rs547432629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160508 | TTTAAAAAAAAAAAA[A/G]TGCAACACCAGACAA | 219333 |
rs547433379 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27065947 | GACATGCTATCACAG[A/G]AAGGTGACACAAGCT | 219333 |
rs547469677 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066635 | TTCCAAGACAGAAGC[C/G]ATGTGACTTAAGAAG | 219333 |
rs547476949 | in-del | -/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067128 | GGCTTTTACGGCATG[-/T]TTTTTTTTTAATGCA | 219333 |
rs547550252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27102791 | TGTCTGCTTCCCCAC[A/G]AGGGTGTCAGGTACC | 219333 |
rs547551805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27087621 | TAGCAACGAGCACAA[C/T]TGTACAAGGTCCTAG | 219333 |
rs547557291 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067280 | TCTTTTTCTCTGTAC[C/T]GAAAGCTGCAGAAAT | 219333 |
rs547603617 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27090303 | AACTACTTAATTTGG[A/T]TTATCCAAAAGGACA | 219333 |
rs547626774 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167763 | TCATTATTTAATATA[A/C]TATTCTTGTTATATG | 219333 |
rs547640392 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126219 | GGAGACACCTCCCAG[C/T]AGGGGCCGACAGACA | 219333 |
rs547653710 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141339 | CTTTTTAAAACATTT[C/G]CTTGCTATGTCCACT | 219333 |
rs547676782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27089004 | TAATCACAGGAAAAC[A/G]AGACAAACTCCAATA | 219333 |
rs547714365 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27102873 | AGGAAATATATCTAT[C/G]ATGATTAGTCTACTC | 219333 |
rs547760945 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141772 | AGTAGAGGTTGAGCA[C/T]CCCTAATTTGAAAAT | 219333 |
rs547763395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153115 | GGCAGGCTGATCACC[C/T]AAGGTCAGGAGTTCA | 219333 |
rs547809515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27102322 | AGAGGACTCCATTTC[C/G]TACCTGGGTACTGCA | 219333 |
rs547849285 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160610 | CTAGTTTTTGAGCCT[C/T]TGATGTTTCAAATTT | 219333 |
rs547875420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27091918 | TCCTTTACCTGTCCA[A/G]ATCCTTCCCACTCCC | 219333 |
rs547914266 | snp | A/G | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27092615 | AGGCAATTCAACAGA[A/G]AAAGAATTGTCTTTT | 219333 |
rs547925847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138538 | TCTTAGGAAACCTGT[A/G]ACCACTGGAGAGGTT | 219333 |
rs547985851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139433 | CCAGCCTGGGCAACA[C/T]GGTGAAACCCCATCT | 219333 |
rs548058748 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167090 | AACATGGAGAAACCC[C/T]ATCTCTACTAAAAAT | 219333 |
rs548071514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123626 | ATGCTCTTCTTGTGA[C/T]AGTGAATAAGTCTCA | 219333 |
rs548086643 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173756 | CTGAGGCATAAGAAT[A/C]GATTGGATCCTGGAG | 219333 |
rs548100333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073185 | CATGAGGCAATGAGA[A/G]TGAGACAGGAGAAAG | 219333 |
rs548126625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127916 | TGCTAAATAACTAAG[C/T]CAAAACCAACAGGCA | 219333 |
rs548250928 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123683 | AGTTCCCCTGCACAC[A/G]CTCTCTTGCCTGCCG | 219333 |
rs548265190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099785 | ATATTAAGAATGCAA[C/G]TGAAGCCACAGTTCA | 219333 |
rs548313816 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169190 | TGCACAGTAAGTATG[A/G]TAAGTGCTACTGAGA | 219333 |
rs548376337 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169612 | ACACGCCCCACATGT[A/T]ATTAATGTATCTGGA | 219333 |
rs548439688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162579 | CAACAACAAAATAAA[A/G]TTAATGCTTTTGAAA | 219333 |
rs548445627 | in-del | -/AAAA | | | intron-variant | USP12 | GRCh38.p7 | 13:27088436 | AAAAAAAAAAAAAAA[-/AAAA]TGGCGTGCTTGCATG | 219333 |
rs548446476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136655 | TTTCTGACTTCTAAG[C/T]GTATACCTATGTTTA | 219333 |
rs548535568 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27073791 | ATGTGGTAATTAGTA[G/T]TATTTACATTTTCTA | 219333 |
rs548550264 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129414 | CAACAGCTCATAAAA[C/T]GACAGTGTCACTCTA | 219333 |
rs548627176 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155948 | TAGATGTACATTCTC[C/T]TTCAATGTTTTTAAA | 219333 |
rs548729446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126921 | ACAAAGCAAACTTCC[G/T]TTGCCCATCTTCCTC | 219333 |
rs548758231 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27077919 | TTTTAAAAAAAAAAG[G/T]GGTCTTAGAACATAA | 219333 |
rs548759775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119580 | TTCATGGCTAAAACT[A/G]TTCAGAAAATTAAAA | 219333 |
rs548778688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166627 | AGCAAAGCCATATGA[C/T]ATAAAATAAGACCAT | 219333 |
rs548779493 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27082088 | TAACCGCTAACCAGA[C/G]AATCAGCCTGTCCTT | 219333 |
rs548781396 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27075952 | GGAGAATCGCTTGAA[A/C]CCAGGAGGCGGAGGT | 219333 |
rs548819999 | snp | C/T | 3.306e-05 | 0.00406558 | intron-variant | USP12 | GRCh38.p7 | 13:27069418 | ACATTAGTACATAAA[C/T]GAGCTCTGTACAGCC | 219333 |
rs548837524 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125210 | CATATTATTTATCAC[A/T]CTAAGTTGAAATTTT | 219333 |
rs548878181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122794 | GAAAACTCAAGTTTC[A/G]TTAAAAACAGGAAAC | 219333 |
rs548884876 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113261 | GACCCTTTCTCAAAA[C/G]AAAAACAAAAACAAA | 219333 |
rs548887851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073008 | GCACCTGTTCTCATA[A/C]GGGAAGTAGACATAC | 219333 |
rs548890302 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27097378 | GCTGAGGCAGAAGAA[A/T]CGCTTGAACCCGGGA | 219333 |
rs548953214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116933 | AACGCTCTGATGTTC[A/G]CATGCACAATGACGA | 219333 |
rs548976165 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27065696 | TGGGAGAATGAAGGA[C/T]GGGCTGAAAATAATG | 219333 |
rs549048431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27108191 | ATATACACCATGGAA[C/T]ACTATGCAGCCATAA | 219333 |
rs549056242 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27079900 | TTTTAAAATGTACCA[C/T]CAACAAGGATTAATT | 219333 |
rs549107160 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155653 | AATATATAACCCTGA[A/G]GCGGAACATATTAAA | 219333 |
rs549108673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27072536 | GCGTAAGGTATGCAA[A/G]TAACTATTGATTGCT | 219333 |
rs549111168 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118170 | CTTTCCGCATGAGAC[C/T]CCTAAATCTGGGAAG | 219333 |
rs549119089 | snp | A/T | 4.96857e-05 | 0.00498401 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116579 | AATCTCTTTCTCTAA[A/T]GCCGAAGCATTGGCG | 219333 |
rs549244374 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153575 | GGTACATTAGAGTTA[A/C]AGATCCTTTTAGTAC | 219333 |
rs549294890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153664 | ACCCACTTTTCTGAT[A/C]CTGTTCTGCTGGATG | 219333 |
rs549339917 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070694 | GAGTAGCTGGGATTA[C/G]AGGCATGCGCCACCA | 219333 |
rs549410260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163861 | GGACTGGCTAAGGGT[A/C]TCCTATCAACCCAGA | 219333 |
rs549429091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145224 | TCCTTCTTGAAGAAT[C/G]ACAGGTGGCCAAAAA | 219333 |
rs549448893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27094869 | AAGAACATGACTGGC[C/T]GGGCATAATGGCTCA | 219333 |
rs549469346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27118759 | AAATACCAGTCCATA[A/C]ACCTTAGGAAGGCAT | 219333 |
rs549509070 | in-del | -/AAAAG | 0.00755907 | 0.0610114 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132434 | ACAGGAAGGCAAAAA[-/AAAAG]AAAAGAAAAAGAAAA | 219333 |
rs549525493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157986 | AATGAATATTCCTTG[A/C]CATTAATTGCAATGG | 219333 |
rs549546000 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152451 | ATAAAGTAAATCAGT[C/G]GTTGCCTAGGGCTGG | 219333 |
rs549566536 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27101285 | GGACTGTATAAACAT[C/T]AAAATAACACTGATG | 219333 |
rs549576193 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129466 | CAGTGGTTCATGCCC[A/G]TAATACCAGCACTTT | 219333 |
rs549596631 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160455 | ATGCAATAAAAACAA[A/G]TGAAACTAACCAGTA | 219333 |
rs549607400 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144811 | CTGCCTGTAATCCCA[C/G]CACTTTGGGAGGTCG | 219333 |
rs549646197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27094458 | AATGATCTATAACAG[C/T]GTCACTGCACTAAAG | 219333 |
rs549704106 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128981 | CTGACTTAGTTTAAT[-/A]AGTAACGGAGTTCAT | 219333 |
rs549730970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27086996 | AAAATCTGAGCTCTT[C/T]CCCTCCCTTAATGAA | 219333 |
rs549757382 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27121427 | CTGGAATGAGACAAA[-/T]TCAATCCACCCACGA | 219333 |
rs549765339 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142071 | AGGGTGCACTGAGCT[A/G]AGATCGTGCCACTAC | 219333 |
rs549814281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160979 | GGCCCCAGTGTGTAG[C/T]GTTCCCCTCCACAAA | 219333 |
rs549876043 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161716 | TCTCTACAAAAAAAA[A/T]TAATTAAAAAGAAAA | 219333 |
rs549879536 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148457 | GAGGCGGGCAGATCA[C/T]GAGGTCAGGAGTTCG | 219333 |
rs549966695 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147476 | AGGTGTCCAATTTTT[A/T]AAAAAATACTTAACT | 219333 |
rs550018948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082315 | AAAACCTCATGAACC[C/T]ACCCCTGCTAGCTTC | 219333 |
rs550021408 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27072855 | CTGACATGCTGATAA[C/T]GAGGCTGCGCACACC | 219333 |
rs550044415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27089137 | AGACCGAATGCTAAA[C/T]GTAATGTGGGATTCT | 219333 |
rs550106838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074388 | CTGGGCCACAGAGCA[A/G]GACTCCATCTCAAAA | 219333 |
rs550144321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146538 | GAAATGTCAGCCATT[A/G]TAAGATTAATGCAAA | 219333 |
rs550160105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151563 | TAGGCAAGAGGATCC[C/T]GAGGGCCAGGAGTTC | 219333 |
rs550168946 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27102920 | TCCATCCCATCAGCA[A/G]GTAACATGCATGGAG | 219333 |
rs550212734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125089 | GTGGACCACTACCAT[C/T]TTCTTTTTCAGTAAA | 219333 |
rs550214236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27083481 | GGGACAGGAAAACAA[C/T]AACTGAAACAGCCAT | 219333 |
rs550248084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27088527 | AAATAATAAGTGTCT[C/T]GCTGTGCCTAAATTG | 219333 |
rs550255391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168153 | GCCTCATTACCACCA[C/T]GTTCTAATGGATCTA | 219333 |
rs550271284 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27106143 | GTAAAGTTTTCTATC[A/G]GGTTCTTAGGTACAT | 219333 |
rs550308333 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27092674 | TCCACATGCAAAAAA[A/T]TTAACCCAGAATAAA | 219333 |
rs550319688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140194 | AAGACATAAAACTCA[C/T]GCAATGTCCCCTGAA | 219333 |
rs550340245 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27107050 | AATCTACTGGCCAGA[C/T]GCAGTGGCTCACACC | 219333 |
rs550380972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131999 | TCACTGGGTAGAGTA[C/T]TGTTCTAGTGCTTCT | 219333 |
rs550384821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27078349 | GGTCATATGCAAATG[C/T]TATGCCATTTTATAT | 219333 |
rs550393863 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27085337 | AGATGTGTGCCACCA[C/T]GCCTGGCTAATTTTT | 219333 |
rs550416963 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163338 | TCACGCCAAACCACC[A/C/T]ACAGAGCCTAAGAGT | 219333 |
rs550423490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070799 | CTCAGGTGATCCGCC[C/T]GCCTCAGCCTCCCCA | 219333 |
rs550433216 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167339 | CTTTTGCTTTCTTGG[A/C]GTTTTTATATTTTCC | 219333 |
rs550440288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132716 | AACAAGAAGAGCAGT[A/G]CTCAGAATAGGAATG | 219333 |
rs550453627 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167638 | AACTCACATTTGAAT[A/G]CTCCTATCATAGAAG | 219333 |
rs550477881 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150738 | ATGAATTAAAATTGA[G/T]GATCCAGAAACTCAT | 219333 |
rs550510038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27071521 | TGAGTTGGACTATAA[A/G]ACAATGCATATAGAA | 219333 |
rs550512313 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27081723 | ATTAAATAATAACAA[C/T]TGAAAGTCAAAATAA | 219333 |
rs550530882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27121663 | TCAGGAAATCGAGAC[C/T]ATCCTGGCTAACACG | 219333 |
rs550540690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125409 | ACACAGGATGTACTA[C/T]AGCAAGTCTGGACAG | 219333 |
rs550542663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134745 | AATAGATAAGCCATC[G/T]TCAATCAGTTTTATA | 219333 |
rs550544769 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126025 | ACTGCCTCTCTAGAT[G/T]CCACCTCTGGGGGCA | 219333 |
rs550561867 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27099900 | AGTTCTAAGAGCTCC[A/G]TACTAGCCTACATGG | 219333 |
rs550579199 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147819 | TCTGCCAATGCTTCC[A/T]TCTAAATGTGAAATA | 219333 |
rs550607726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143765 | CAAAAATGTTTACTC[A/G]CAGTCTAATCAAGCC | 219333 |
rs550672316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136743 | TGCATTATATGGTCC[A/G]TATGCTCAGGGAGCA | 219333 |
rs550686326 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27085892 | TACTATGCAGCAGGC[A/G]TGGTATCTAGCTCCT | 219333 |
rs550706235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162645 | TGTGACAATACTATC[A/G]TGTTACTGTTAAAGA | 219333 |
rs550769536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156104 | CTCCGTAACAGAAGA[A/G]TCATTCTGACAATGC | 219333 |
rs550772728 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116876 | AGGCTCTACCATCTA[A/G]CCTAGGTGTGCAGTA | 219333 |
rs550778891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128494 | AACATTTAAAACATA[A/G]CTATATCTGAACTCC | 219333 |
rs550834116 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171703 | GGAGGAGGGGAGCCG[A/G]GCCGCCCGCTCGCAC | 219333 |
rs550850977 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113322 | AAAAAATAAAAATGT[A/T]GAAAAGGAACCGTTT | 219333 |
rs550852440 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170602 | TCTGGCCACGCACAA[A/C]ACACCAAGTTTTAAA | 219333 |
rs550902775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122256 | GGTGGTTCCCCCATA[C/T]TGTTCTCGTGGTAGT | 219333 |
rs550947389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122774 | GTCAATGTAAGGTTA[C/T]TAATGAAAACTCAAG | 219333 |
rs551008824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27123460 | GCATCATATCCTCAA[C/T]AATAGCCATCCAATA | 219333 |
rs551019359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27075642 | CAATATGGCTCCAAA[A/G]CAGATGGAATGGCGT | 219333 |
rs551028443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151095 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAC | 219333 |
rs551038900 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27069839 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 219333 |
rs551054222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27075965 | AACCCAGGAGGCGGA[A/G]GTTGCAGTGAGCTGA | 219333 |
rs551099659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170304 | ATCTGCTTTTTAAGG[C/T]ATCTTTCAGATCTGA | 219333 |
rs551109910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27120517 | AAATTAGTCAGGGGT[A/G]GTCGTGGGCGCCTGT | 219333 |
rs551138557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27069996 | ATATATCCAAGAAAA[A/G]TGAGTGTATACGTCC | 219333 |
rs551198617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113706 | CCTAAAACAGGGCTG[A/G]ACGCTTGGTACAGTC | 219333 |
rs551233853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154374 | TTATCAAAAGTTGTA[A/G]AAGTATTGGTAGCTA | 219333 |
rs551240748 | in-del | -/GCATGTGAT | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27081178 | ACAGATTTCTCTGTA[-/GCATGTGAT]GCTGTTTGACAGCAT | 219333 |
rs551253098 | in-del | -/T | 0.0138799 | 0.0821421 | intron-variant | USP12 | GRCh38.p7 | 13:27088292 | GTGGTGGCGGGCGCC[-/T]GTAGTCCCAGCTACT | 219333 |
rs551275313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27107257 | TTGAACCTGGGAGGC[A/G]GAGGCTGCAGTGAGC | 219333 |
rs551294421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160162 | TAAACAGAGAACAAA[A/G]AAAGGTGACAGATTT | 219333 |
rs551353551 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153282 | ACTGCACTCCAGCCT[C/G]GGCAACAGAGTGAGA | 219333 |
rs551402141 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173710 | AGCCAGGCGTAGCAG[C/T]GTACGCCTGTAATCC | 219333 |
rs551419578 | in-del | -/GG | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27083024 | ATTTTTAGTAGAGAT[-/GG]GGTTTCACCATGTTG | 219333 |
rs551423680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166704 | GAGTTTTCAAGCATA[G/T]TAAAAATTTCAGATC | 219333 |
rs551447084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073151 | CAAGGAAGACTTCCA[C/G]AGCGGAGGGGCAGGA | 219333 |
rs551451456 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27097014 | TTAAAAAAAGTGAAA[C/T]CTGAAAATTATTAAC | 219333 |
rs551468732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117153 | CTTTTGATAATGACT[A/T]AAAATTCGTTTATAG | 219333 |
rs551470962 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27070182 | CACAAATATATCAAT[A/G]AGTGAATAAAGTCTG | 219333 |
rs551549129 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166874 | TACCACTATGCTTTA[C/T]TGGGCTCATCTCACC | 219333 |
rs551563569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27095151 | AACAATTTTCAAGCT[C/T]CATCTTTACAAAGTG | 219333 |
rs551619132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144844 | ACAGGCAGATCCTTT[A/C]AGCCCAGGAGTTCGA | 219333 |
rs551621802 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156107 | CGTAACAGAAGAGTC[A/G]TTCTGACAATGCCAG | 219333 |
rs551628290 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27121588 | GATATTAAGGCAGGC[A/G]TGGTGGCTCATGCTT | 219333 |
rs551735825 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132145 | TTTCCTCCACCTCCC[A/G]GCCACTTACTCATAT | 219333 |
rs551793197 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27108815 | TTACAAAAATTAGCC[A/G]GGTGTGGTGGCACGC | 219333 |
rs551819754 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132550 | TGTCCTCAAGTGTCT[C/G]GAAATCCCTGGTTGG | 219333 |
rs551840549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27112741 | GGAACTTGAAATAAC[A/G]TACAACCATATCATA | 219333 |
rs551921058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27090967 | GCATAGTGTATTTTA[C/T]AGACAGTTGAAGGGA | 219333 |
rs551949173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145445 | TTAGAAATCAATCAG[G/T]TAGGCTTCCTGCATA | 219333 |
rs551959597 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27091799 | GAAAAGGAACCCTCA[G/T]AGAGAACACCAGAAA | 219333 |
rs551998831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155886 | ACAACTATGAAAATA[C/T]TCTGAAAATGTAAAA | 219333 |
rs552064697 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142533 | TTAAGTTTTTACGAA[C/T]GTACACACAAATATA | 219333 |
rs552145970 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173076 | CTGTTTCCATAGTGA[C/T]TCCATTATAAGCTTG | 219333 |
rs552154209 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27098092 | AAGTAAATTTGTGTA[C/T]ACTGAACCATCAGAA | 219333 |
rs552190404 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172714 | AGAAATCCTTAGGCA[A/G]TGCTGGCTACTGGCA | 219333 |
rs552240173 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117999 | TACCTTGAAAATTCC[C/T]GGGAAAACATACTAG | 219333 |
rs552254479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149294 | TATCTTACTTAATAG[C/T]GAAAACACTGGATGC | 219333 |
rs552256407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155872 | ATGACTTTCGGAATA[C/G]AACTATGAAAATATT | 219333 |
rs552349194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141193 | GCTAATTTTTGTATT[C/T]TTAGTGGAGACAGGT | 219333 |
rs552368175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27074441 | AGAGAGCTGGGAGGA[A/G]GGCTGAAGATGAGAA | 219333 |
rs552404993 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067577 | AGCAGCCCAATTAAG[A/T]GACTCTGTTAAAGGT | 219333 |
rs552408645 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27088670 | AGGGCACTCAGTCTG[G/T]AATGAGCTTCCTGTG | 219333 |
rs552416269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082352 | TTCTTCTGCAGCTTC[A/C]TTACCTCTCTCAGCC | 219333 |
rs552469044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136017 | GAGATCAAAATATTA[C/T]TTTAAACAGACCCCA | 219333 |
rs552490929 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068713 | TATACTGTATATTAT[C/T]ATAAGCTTCTTCAGA | 219333 |
rs552495064 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27086682 | GAAAGGGTGGCTTTT[A/G]CTCACAGATGGGCCT | 219333 |
rs552539843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140271 | AGAAGTACTGATGAC[A/G]TTCTATTTCTTAATA | 219333 |
rs552541432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27089226 | GGTTTGCAGTAACAG[A/T]AGCATGTCAGTGTTA | 219333 |
rs552546785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27169853 | ACTCAGCGTCGCCTC[C/T]AGCACTTAGTGGCTG | 219333 |
rs552562748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170566 | ACGAATTTGTCTCAT[C/T]ATGTGGAAAACTGTG | 219333 |
rs552564020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27169084 | ATACTGAATGCAGAA[C/T]TTGGTACTCCAGATC | 219333 |
rs552573383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27096826 | TTTAGATCCTCAATG[C/T]ACATTTAATAAGTTC | 219333 |
rs552602341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132066 | AATTCTCATATAGCA[C/T]GTAAGAAATCCGGGC | 219333 |
rs552628336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171184 | CGACGACCCCGGCCC[A/G]GGGCCGCGCTCTGGC | 219333 |
rs552642854 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070418 | GTGTGAGTATGGCCA[A/T]GTGTGTGTGACATGG | 219333 |
rs552679649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070843 | CAGGCGTGAGCCACC[A/G]CACCTGGCCTCCCTT | 219333 |
rs552804381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161088 | TCTATTAAGATATAC[C/G]TCCTAACGCAAACTT | 219333 |
rs552833788 | in-del | -/AAT | 0.0825414 | 0.185628 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165926 | CTACAGAGCAAAAAA[-/AAT]AATAATAATAATTTT | 219333 |
rs552837284 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138759 | CATTTGCTATGTTTC[A/G]GGTAGTGTTTGCCTT | 219333 |
rs552852415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125827 | CCTGGCTTATGGGTC[C/T]CACGCCCAGGGAGCC | 219333 |
rs552910226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128046 | TTTCAATGAAAAGTT[C/T]CACCACATAATTCAT | 219333 |
rs552919610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119445 | ATCGTTTAACCCTTC[C/T]GGATTTAAGAATCTT | 219333 |
rs552938868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27077544 | ATATGAATCCTATTT[C/G]CCAAAGATCCTCCCA | 219333 |
rs552947690 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27121017 | CTTCTAACAGCTGAA[G/T]GGAACGGTATGCAGG | 219333 |
rs552978432 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143803 | CTAATTCCCACTTTA[C/T]AGAAAATATAACGGA | 219333 |
rs552984482 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151443 | GAGGAAATATTAGCA[A/C]ATAAGGTAACTAACA | 219333 |
rs553018840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149678 | ACAAAATTACAGCTC[A/G]ATAGGAGGAATAAGT | 219333 |
rs553054015 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27113110 | CATGGTGGTGTGCAC[A/C]TGTAGTCCCAGCTAC | 219333 |
rs553126318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27114246 | AAAAAATGCACAGAC[C/T]ATATTACAAGTAAGA | 219333 |
rs553128155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27121778 | AAGCAGGAGAATGGC[A/G]CGAACCTGGGAGGCA | 219333 |
rs553132940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157548 | TTAAAAAAAATATAA[C/G]TTTATAGAAGATTTT | 219333 |
rs553139594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142732 | TGAACATCACCAAAA[A/C]GAATGACTGTAATTT | 219333 |
rs553140064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27106146 | AAGTTTTCTATCAGG[C/T]TCTTAGGTACATCCA | 219333 |
rs553165307 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27115328 | CCTGTTCTGGAGAGA[C/G]AGAAAGGTAAGGGAG | 219333 |
rs553200942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143202 | TCAAAAAGAATGATT[A/G]TAATTGATTATTATC | 219333 |
rs553238682 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142150 | CAGACACACACACAC[A/G/T]CAATGACAGTGAAGA | 219333 |
rs553267457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152103 | CTGGTAGATCCTCAA[A/G]AGATTAAACCACAAT | 219333 |
rs553281279 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172589 | GATAAATTTATAATA[C/G]GCTTCTAAATATCTG | 219333 |
rs553328810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152709 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 219333 |
rs553332980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144118 | CTGAGGTGGGAGGAT[C/G]ACTTCAGCCTGGGAG | 219333 |
rs553337215 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162681 | CCCTTTCATTTTAGG[A/T]AGGTTTCTTATTGAG | 219333 |
rs553357887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113367 | CTTCTTCCCTGTCCC[C/T]CATGCTGGGCCTGGG | 219333 |
rs553368084 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118296 | TCCACCAAAACAAGA[C/T]GTTTCTTCTATTATC | 219333 |
rs553400532 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156123 | TTCTGACAATGCCAG[A/C]CTCATCATTATAAAG | 219333 |
rs553406187 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127440 | AGAAATGAAATATTG[C/T]ACAACCAGTTATCAA | 219333 |
rs553474693 | in-del | -/AA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159323 | TACCACCCCATTTCT[-/AA]AAGTTACCATGACAT | 219333 |
rs553480695 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146854 | TAATCAAGTTAAAAT[C/G]AGGTCATGAAGGTAA | 219333 |
rs553489523 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27098730 | CCAAAACAAGCATAA[A/G]TACGGCTGCTTATTT | 219333 |
rs553517365 | in-del | -/AAATTCATC | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27070450 | GGGACACATGTATAA[-/AAATTCATC]AAATTCAGATTTGTA | 219333 |
rs553542049 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139685 | TCCTATAGCAATTTC[A/C]TACATGCAAGTCCCA | 219333 |
rs553573869 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27103117 | TTAAAACAATATGGG[G/T]CTAATATCTATTGAG | 219333 |
rs553605839 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140337 | TGAAAACTCATTGAA[C/G]TTTACATTTATGTGA | 219333 |
rs553643638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136313 | GACCAGCCTGGCCAA[C/T]ATGGCGAAACCCCAT | 219333 |
rs553682552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27092836 | ATACAACACCAAAAG[C/T]ATAATGCATGAAAGA | 219333 |
rs553688573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109556 | AAAGGACTCAAGAGA[C/T]ACAACAATCAAATTG | 219333 |
rs553759307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27094601 | TTGTGTGCCTACAGA[C/T]GTGATGCCCCGAGAA | 219333 |
rs553797886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132119 | ACATTCACCTTTCCT[C/G]CTATCCCTCATTTCC | 219333 |
rs553854760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27101700 | AGGTTATGTTCTCCT[C/T]ATAATTCAGAAATAG | 219333 |
rs553873400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137088 | AAAGATAGTGAACAA[A/G]CTGCATTTGTTCAGA | 219333 |
rs553890930 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27095919 | ATATCTAGTATTGGA[A/T]CAGAACTAAAATATA | 219333 |
rs553902095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125175 | TTCAATATGTAAGTA[C/T]GTATGTATGTATTGG | 219333 |
rs553926365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122464 | TTGGCAGTGTGGAAA[C/T]GGACTAATACACCCC | 219333 |
rs553986133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122809 | GTTAAAAACAGGAAA[C/T]GTGGCCAGGCGCGGT | 219333 |
rs554016176 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27088640 | ACCTACATGACTAGC[A/C]CCAAATAAAAACTCA | 219333 |
rs554051896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123965 | GTGAAATAATAATAG[A/G]TTGAAATTACAAAGA | 219333 |
rs554065627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116769 | TGTACCTTTCTTACG[G/T]TTAGATATGTTCAGA | 219333 |
rs554077115 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27080302 | TGCTGATATGATTTT[C/G]ACATGATACTACACA | 219333 |
rs554103513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27089312 | ATACCTATTAAAGTG[C/T]CGGGGCCATGAGGTA | 219333 |
rs554118650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27090473 | CTGTACCATATACAC[C/T]GATTCTTAAAAAAAC | 219333 |
rs554120483 | snp | C/T | 0.124491 | 0.216211 | intron-variant | USP12 | GRCh38.p7 | 13:27108218 | ATAAAAAATGATGAG[C/T]TCATGTCCTTTGTAG | 219333 |
rs554142141 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27081697 | CTATGGCAGCTGTAG[A/G]CTTAAAAAATATTAA | 219333 |
rs554151183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27091032 | ACATTAAGCTAACCA[C/T]AGGACCGAAACCCCT | 219333 |
rs554155332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082881 | ACTCTTGTTGCCCAG[C/G]CTGGAGTGCAATGGC | 219333 |
rs554162920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27072739 | AATGGTGCCCAGTTT[G/T]GACATGGGCTTGAAG | 219333 |
rs554210409 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138623 | GCTGCGGGAAAGCCT[C/T]GGTATGCAGGAGTCA | 219333 |
rs554226824 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139052 | TTCTTATTCTTTTTA[C/G]TTTGTTACACTTGCA | 219333 |
rs554239228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27083604 | AGTGACATTTCCCAC[A/G]CTGCTATCTTTCCTG | 219333 |
rs554244885 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27079231 | GGGCGGGGGGGAGTG[A/G]GGGGAGAGGGAAGGA | 219333 |
rs554245771 | in-del | -/AAACAAAC | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27113270 | TCAAAACAAAAACAA[-/AAACAAAC]AAACAAACAAACAAA | 219333 |
rs554275951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27084616 | TTCGTGTGGATATTC[A/G]GTTTTCCCAAAACCA | 219333 |
rs554316608 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27102960 | CTGTACTCTATGCAG[C/G]AGCACTGTGCAACAG | 219333 |
rs554369020 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, nc-transcript-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172267 | CACCCACCGCGGGCG[A/G]GGGGACGGCGAGCCC | 219333 |
rs554376132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27113160 | GGACGGCTTGAGCCA[A/G]GAAGGTGAAGCTGCA | 219333 |
rs554385937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126572 | TGGGCAGGGGACTGG[A/G]TGACAGCCTTCAAAC | 219333 |
rs554400396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27075755 | AGAGGGAAGGCCAGG[C/T]GCGGTGGCTCACGCC | 219333 |
rs554420024 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173160 | GATCTCCAAGCGCCT[A/G]CCTCCATGGAAGCCA | 219333 |
rs554462193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113449 | TTGCACCAACCAGTT[A/C]TTGTTTAGGTGACAT | 219333 |
rs554464645 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27106566 | GGAGCACTATGAAAC[C/T]ATAAAAAAGGAATGA | 219333 |
rs554477474 | in-del | -/TG | 0.097727 | 0.198275 | intron-variant | USP12 | GRCh38.p7 | 13:27079209 | TAATGTCGTGCTCCC[-/TG]TGTGTGGGGCGGGGG | 219333 |
rs554523926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27098409 | AAAAAATTTTAAAAA[C/T]TGGCAAAGGAAAATA | 219333 |
rs554568374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167694 | TTTACAAATAAATAT[C/T]TTATTAATAAAAGAA | 219333 |
rs554627835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160862 | GACACAGGTAAACGT[A/G]TCATGGTGGTTTGCT | 219333 |
rs554629653 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168461 | CACCTCAACTGCAAA[A/T]CACAGCCTCTCTACA | 219333 |
rs554634341 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27100347 | CCCAACCCTTTCTAA[A/G]TTGCTCATTCTAGGT | 219333 |
rs554645088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124672 | GGTAAAATAAGAAAA[A/G]TTCTGGAGGCACAGG | 219333 |
rs554661600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134206 | CCCTATAAATGAAAA[A/G]GACTAAAGAAGCTCT | 219333 |
rs554730173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127315 | ATCAGAAATCGGCAC[A/G]AAGCAAAGTGACCCT | 219333 |
rs554738509 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161679 | AGTTTGAGACCAGCC[G/T]GGGCAACATGGTGAA | 219333 |
rs554766052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169387 | ACCTACAAAGCCAAA[A/G]AGGTATCTTTGCTTT | 219333 |
rs554771134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27076409 | ACCTAAAAATCTATT[C/T]TTCTTTTAATGGCTC | 219333 |
rs554782005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27120254 | ATTCAATAATAATAG[C/T]TCCATTCCCACATTT | 219333 |
rs554807855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27069667 | AATGGTAACTTCTAG[G/T]CTGGGCACACTGACT | 219333 |
rs554825578 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27170030 | AGACCTAATTATCGC[A/T]TTCCTTTTGAAATTG | 219333 |
rs554827554 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162182 | CAAAGGACGTTCACA[A/T]GTGTCATCTCATCTG | 219333 |
rs554874056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155273 | TTTTTAGTAGAGACA[G/T]GGTTTCACCATGTTG | 219333 |
rs554908811 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27105004 | GAACACTGGGCTTAC[A/G/T]TATCAGGGAGAAGTA | 219333 |
rs554910887 | snp | A/G | | | intron-variant, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27101552 | AAATGGGTTCCCTCC[A/G]TCATGGAACTGACAG | 219333 |
rs554937027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148732 | AAGAGGTAGGTTGAA[A/G]TGGGCTAACATAAAA | 219333 |
rs554975681 | snp | C/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068013 | AAGATTTGTAAAGGT[C/G]GGGGGAAGGGAAGGA | 219333 |
rs555004895 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074595 | GTTATGTTCCAAATA[C/G]AAGTTTTGATTATGT | 219333 |
rs555029877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165104 | TAGATTTTTCTTCTA[A/G]AAGTATTAGATTGTT | 219333 |
rs555036251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118255 | AAGGGGACTGATAAA[A/G]GCACATGGTGAGTTG | 219333 |
rs555090697 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27172063 | CTTGTGCGCGAGCCG[C/G]GGAACTCCGGTCCGT | 219333 |
rs555090839 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067793 | ACATCCAAGGCCTGA[A/T]TGCTATTATTCTGAA | 219333 |
rs555093304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154858 | AGCAGGACAGTCGCC[A/G]TCCGAGGGAGGTAAT | 219333 |
rs555230005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27105714 | TATGTCATTAATACA[A/G]TGGGAAGTAGAATTA | 219333 |
rs555271190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149511 | AAATTACTACTAGAA[C/T]AAACGAGTTCAGCAA | 219333 |
rs555301749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171280 | GAGCGGACCCCAGCA[A/G]TTCAGCCGGGGACTC | 219333 |
rs555324885 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068933 | TACGGCACAGATTCC[A/G]ATTCTTTCTACTGCA | 219333 |
rs555336268 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27121848 | CCTGGGAGACAGAGC[A/G]AGACTCTGTCTCAAA | 219333 |
rs555347529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153193 | CAAAAATTAGCCAGG[C/T]GTGGTGGCAGGCACC | 219333 |
rs555357939 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27111582 | CAAAGAGCTTTCTCT[A/C]ATGCCTTCTTCTCCA | 219333 |
rs555386728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27107441 | CTTAGGAACCAAAAT[G/T]TTTAATGTAAAGGAA | 219333 |
rs555392089 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154854 | GGGAAGCAGGACAGT[C/T]GCCGTCCGAGGGAGG | 219333 |
rs555406803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145755 | TCTGTAACTCTATAC[C/T]ACAAAATTTTGTTAT | 219333 |
rs555407220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122488 | ACACCCCATCTTTAC[C/T]GAAAATACAAAAAAC | 219333 |
rs555443965 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27119609 | AAGATTATGTGATTT[A/C]TAAAATCCCTTCTCA | 219333 |
rs555444474 | in-del | -/T | 0.177824 | 0.239355 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160782 | AAAGCATCATGTTTC[-/T]TTTTTTTTTTTTTCC | 219333 |
rs555527821 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27070458 | TGTATAAAAATTCAT[C/T]AAATTCAGATTTGTA | 219333 |
rs555537288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144001 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGGC | 219333 |
rs555550221 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152771 | CACGGTGAAACCCCG[A/T]CTCTACTAAAAATAC | 219333 |
rs555558948 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP12 | GRCh38.p7 | 13:27108972 | TGTGTGTGTGTGTGT[A/G]TATACACATAATGAC | 219333 |
rs555582321 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155163 | CTCGGCTCATTGCAA[C/G]CTCCGCCTCCAAGGT | 219333 |
rs555582944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27101828 | ACAGGTATTATTTGT[A/G]AACAACTAAAATTTC | 219333 |
rs555683241 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150771 | ATCTCTGATCAACTG[A/G]TTTTCAACAAGAGTG | 219333 |
rs555694968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27103316 | TTGTATATTCTTCTC[C/T]ACACAATTCTCAAGG | 219333 |
rs555781864 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27075914 | AGGCGCCCATAGTCC[C/T]AGCTACTCGGGAAGC | 219333 |
rs555782343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170655 | CGGGACTTCCAGCGG[A/G]CATTAGCACTTTTCC | 219333 |
rs555847818 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142521 | GGAAATGTGCACTTA[A/G]GTTTTTACGAATGTA | 219333 |
rs555903037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27092987 | GGATCACTTGAGGTC[A/G]GGAGTTCAAGACCAG | 219333 |
rs555915026 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156449 | GAAACGCAACGATGA[A/T]CATTATGGATCCAAC | 219333 |
rs555936167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132405 | CATAAAATATCATTC[A/C]AATAAAAAGCAGTAC | 219333 |
rs556021255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140597 | GTACCCTCAAAATAA[C/T]CTTAGAAGATACTAT | 219333 |
rs556026287 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130563 | TCACAAAACATGCCA[-/A]AAAAAAAAAAAAAGG | 219333 |
rs556049871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27089472 | TATTGATACCAAACC[A/C]GTCTTACAATAACAT | 219333 |
rs556059447 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126713 | CACCTATTGCAAACC[C/G]AAAATGCTACAATTC | 219333 |
rs556096173 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124607 | ACACAAAGGAGAACC[A/G]CCAAATCAGGCAGGA | 219333 |
rs556097449 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | USP12 | GRCh38.p7 | 13:27109502 | TCTAGGACAGATGAC[A/C]TAGTTTCTCCACAAA | 219333 |
rs556136561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147099 | TCTGGAATCCAGAAT[C/T]GTAAGATGACCAATG | 219333 |
rs556187399 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141074 | AGGCTGGAGCGCAGT[C/G]GCACAACCTCAGCTC | 219333 |
rs556202376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154768 | GTTGCTAAAATCAAA[C/T]GACCTTGAGAGAGTA | 219333 |
rs556205852 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161643 | AATTGCAGCATTTTG[G/T]GAGGCCAGCTACATC | 219333 |
rs556219132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070803 | GGTGATCCGCCCGCC[C/T]CAGCCTCCCCAAGTG | 219333 |
rs556254317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27095532 | ATCTTCCATTCTGTC[C/T]TTCTCAAAGAACAAC | 219333 |
rs556333292 | snp | A/T | 1.65255e-05 | 0.00287445 | missense | USP12 | GRCh38.p7 | 13:27090132 | GTCAACAGAAAGGTC[A/T]AAAAAATCTTCATCT | 219333 |
rs556382456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124835 | AAGGCTTAACCCTCA[C/T]ACCTGTTCTAGAAAA | 219333 |
rs556495972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074127 | CATCAGAGGCCGGGC[A/G]CGGTGGCTCACGCGT | 219333 |
rs556502461 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27073225 | CTGGGGTGGGGGCGG[C/G]ATACCAAAGACCTGC | 219333 |
rs556534487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074701 | GATGTGTATACCATG[C/T]TGGAAAAGAAGATGA | 219333 |
rs556539422 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27066114 | TCTAATCTGTAAATA[C/T]ATTTTAGGCAAAAAG | 219333 |
rs556591721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138612 | TTTTTGACTTTGCTG[C/T]GGGAAAGCCTTGGTA | 219333 |
rs556602118 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27108504 | TAACCTGCACATTGT[A/G]CACATGTACCCTAAA | 219333 |
rs556643530 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143086 | AACAGAGTGAGACTC[C/T]GTCTCAAAAAAAGAA | 219333 |
rs556649089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27083798 | ACTAATTTTGTGGCA[C/T]ATCATTAACATTCCC | 219333 |
rs556654366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27072799 | AGAAGTCTCTTCTAG[A/G]CTGGGCACCGGGGAC | 219333 |
rs556709627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116806 | CTTATTCCTGTGTTA[C/T]GATTGCCTAGAAAAT | 219333 |
rs556736620 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27078595 | CCATGTAAACACTAA[C/T]CCTAAGTAAACTGGC | 219333 |
rs556751601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070405 | TACAAATGTGAGTGT[A/G]TGAGTATGGCCATGT | 219333 |
rs556775329 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076269 | AGAAAGGGAGTAAAA[A/T]AACCTGGAAACTTAG | 219333 |
rs556819796 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130228 | GCCTGGGGAAACAGC[A/T]CAGATTCTTGCTTTT | 219333 |
rs556820765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162952 | CTTAATTTTTTAACA[C/T]GTATATACAATCCAA | 219333 |
rs556865051 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101418 | AGGTGGACTTCAAAC[C/T]TGCTTTGGAAGTTAA | 219333 |
rs556867585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27113474 | TGACATTTTAGAACA[C/T]TGTATTTCCACATCC | 219333 |
rs556877537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159842 | ATAAAATGGCAAGAA[A/C]ATCACGGTAGGCTAT | 219333 |
rs556881068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27092072 | GTGATCAGAGGCTTA[A/T]GTCTTACTCATCTTC | 219333 |
rs556900241 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133197 | CTATCCTCTAGCTCT[A/G]TTCCAGTTCAATAAA | 219333 |
rs556915342 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27096037 | AATCTTGTTTAAAAA[C/T]ACTACTAATTGATCC | 219333 |
rs556941051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154117 | AGTTGCCCTTTTCTG[A/C]CCTTTCTTCCTTAGG | 219333 |
rs556958088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161186 | AAATTAAACAAACAG[C/G]GAACCTTTGCAACAT | 219333 |
rs556993549 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135434 | TGGGTCTATGGAGGC[C/T]GGGCATGCTGGCTCA | 219333 |
rs557019600 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162029 | AATGACTACGCTTTG[A/T]CAAAGGTAACTTGTG | 219333 |
rs557053891 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127389 | GTTCAGCTGCCAACA[C/G]TAATGGAGAAGTCAG | 219333 |
rs557061857 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170459 | GAAGTCTCTAATAAC[A/C]ACCACTAGGCCCACG | 219333 |
rs557078816 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155575 | ACCTGGTTAGTTCAT[C/G]TAATTTTCAGAATCC | 219333 |
rs557096802 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27087122 | GTGTGTGTGTGTGTG[C/T]GCGTGTGTGAGAGTG | 219333 |
rs557100445 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068022 | AAAGGTGGGGGGAAG[A/G]GAAGGAAGGACTTGT | 219333 |
rs557116025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128028 | GATTATTTTATTCAG[C/T]ATTTTCAATGAAAAG | 219333 |
rs557132579 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27089500 | CATGCTAAGAGAATG[C/T]ACAACATCCTATGTA | 219333 |
rs557139793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163403 | CTCCATGTCCACATA[A/C]TAAAGGCCATTCATT | 219333 |
rs557257303 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27113538 | AGACCAGACATTGAG[C/T]ACCTCACCCAGAAGT | 219333 |
rs557265856 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151747 | ACTACACTCCAGCCT[A/G]AGTAACACAGCAAGA | 219333 |
rs557277469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156873 | ATGGTTGTCTTTAGG[G/T]GGAAGAAGCATCTAC | 219333 |
rs557320864 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069279 | TCTTCATCACGGTTC[C/T]CTCTCAGTCCCGAGA | 219333 |
rs557334488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158393 | CTAGCCTACAGAATT[C/G]TTAGGACGATAAATT | 219333 |
rs557339138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151309 | AAGCAAGATTCTGTC[C/T]CCCAAAAAAAAGGAA | 219333 |
rs557343717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169274 | GGGTAGGATTATTCA[A/G]GTAAGGCTCCCTGCT | 219333 |
rs557387240 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068956 | CTACTGCACCCCCAA[A/G]GAATTCAAAGCATTA | 219333 |
rs557398334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152835 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 219333 |
rs557474333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166176 | ATTTACCTTCTGGTC[C/T]AACTGCTCTTTTCAT | 219333 |
rs557508349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27105280 | GTGGCTCCTGGCAAG[C/T]CTTTTTTAGGTTTTG | 219333 |
rs557546251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106038 | AACAGAAAGAGATGA[C/G]AATCGGTTACTACTG | 219333 |
rs557583751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146743 | CATCCGTTATGCATT[A/G]AACTATGCACCCCCT | 219333 |
rs557607201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150454 | AAGGAAATCTAAACA[C/G]AGAGAAAAACATACC | 219333 |
rs557630106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27098627 | TAAACTGGTATGGCA[C/T]GTTGTAAAGGCAATT | 219333 |
rs557685934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27108239 | TCCTTTGTAGGGACA[C/T]GGATGAAATTGGAAA | 219333 |
rs557685953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27100147 | GTGGTTCCACCAATT[A/G]GAAAAGTCTAGACCA | 219333 |
rs557722025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134268 | GAATTTGGAGAAAGG[C/T]AGCATAAAAGAAAGC | 219333 |
rs557762291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109087 | GCCTTTCTTATAAGA[A/G]CCATATTTCAGGGGC | 219333 |
rs557784071 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27071887 | TATGGTTCATTATAA[A/T]GGCTCATATAATTAT | 219333 |
rs557803402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139584 | TCGCGCCACTGCACT[C/T]CAGCCTGGGAGAAAG | 219333 |
rs557903329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27093133 | CCCAGGAGGCAGAGG[C/T]TGCGGTGAGCCACTG | 219333 |
rs557929649 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128821 | CACTTATAAAAACAT[C/G]AACGCTTCTATTTTT | 219333 |
rs557980154 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27096275 | ACATCCCAGGGATTC[C/T]GATTTAGTTGATAAG | 219333 |
rs558014310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27087836 | GAGATAATGTGAGCA[C/T]GGAAGTAAGAATGCT | 219333 |
rs558052016 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27079893 | CATGCCCTTTTAAAA[G/T]GTACCATCAACAAGG | 219333 |
rs558052559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122424 | ACTAAAACTCTTTTT[C/T]TTCACGGTCTTGGGT | 219333 |
rs558053608 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27118732 | TCAAATACTTACCCA[A/T]CTAGAACAATAAAAT | 219333 |
rs558054015 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27089823 | GTTTTTCTAAGCCCA[C/G]CTCCAACATCAATTA | 219333 |
rs558057600 | in-del | -/AAAAG | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27106862 | TCTTTTCTAAAATAA[-/AAAAG]AAATGTCTAAAATTA | 219333 |
rs558065033 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123981 | TTGAAATTACAAAGA[C/T]ACCTTTGACCTATTA | 219333 |
rs558065263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137767 | ACCAGTAGAAAATGA[C/T]GGAAGAGATGGGATG | 219333 |
rs558065925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27096404 | CCAGATAATCTCAAG[C/T]CCCTTCCAAATGTGA | 219333 |
rs558082890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27097250 | GCAGGTGGATCACCT[A/G]AGGTAAAGAGTTTGA | 219333 |
rs558085534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171310 | CCCGGAGGCCGGTGC[A/C]CGCCCGACGCCGCGT | 219333 |
rs558204843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144050 | CTCTACTAAGACTAT[A/G]AAACTTAGCCAGGTG | 219333 |
rs558208488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27093680 | TCCTTGATATTTACA[C/G]AAAGGAAGTAAAAAC | 219333 |
rs558238164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27108513 | CATTGTGCACATGTA[A/C]CCTAAAACTTAAAGC | 219333 |
rs558320772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141607 | CATCAGGAACAATTT[A/G]GGTATCAAAATCAAT | 219333 |
rs558368895 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126344 | GGCAAACAGGGTCTG[C/G]AGTGGACCTCCAGCA | 219333 |
rs558373351 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141948 | GCACTTTGGGAGGCC[-/A]AAAAAAAAATACAAA | 219333 |
rs558411317 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27172114 | AGGGCAGGACCGAAG[C/G]CGGGCGCCACCTCCT | 219333 |
rs558450170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119662 | TCACTTTCATGAATG[C/T]TTCTGAAGACATTAC | 219333 |
rs558477238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27074853 | GATATGCTGAACATA[C/T]GCAATTAAACTCAGA | 219333 |
rs558478705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104923 | GCCTACATTAAACAA[A/T]AGCCAGAATTCTACA | 219333 |
rs558479788 | snp | A/G | 5.04494e-05 | 0.00502217 | intron-variant | USP12 | GRCh38.p7 | 13:27071161 | ACCACTAAAACAAAC[A/G]AAGAAGAAGTTAATT | 219333 |
rs558513947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27072108 | AACAAAAATACTTTT[C/T]TTTTTTTAACTATGG | 219333 |
rs558576250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148563 | CCTGTAATCCCAGCT[A/G]CTCAGGAGGCTGAGG | 219333 |
rs558647018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27169018 | CAGCCACATCATCCC[C/T]GCTTCACCCGGCATA | 219333 |
rs558679010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131122 | CATATGTTAAACACA[A/G]TTTGAATACAAATTC | 219333 |
rs558682761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27081053 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 219333 |
rs558694035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133962 | CACAGTGAAATCCCA[C/T]CTCTAAATAAATAAA | 219333 |
rs558712588 | in-del | -/TAAT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139227 | TACCCTTCATCTGAG[-/TAAT]TAATTTCTATAATGC | 219333 |
rs558741932 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066891 | ATTTTTCCCCCAACC[A/C]TGACCCTATACGTTT | 219333 |
rs558825499 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167508 | GACCAAACATTTATG[C/T]AATAGAAGATTCCTT | 219333 |
rs558879922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27080448 | AGGGCAGATACTCAG[A/G]GATGGACTGTGGCCA | 219333 |
rs558883484 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068147 | ACTTCTTTCCAGGGT[A/C]AAAAATGGCATCTGA | 219333 |
rs558911292 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27110942 | AGTATACCAGAAATA[G/T]TATGATAATGAGGAT | 219333 |
rs558920423 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069028 | AAGGCTGTTTTAAAA[A/G]AGGAGCTGGTATCTC | 219333 |
rs558930084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27069861 | CTGAGGCAGGAGAAT[C/G]GCTTGAACCCAGGAG | 219333 |
rs559001968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27104107 | GCAATCAGGGCTCAC[C/T]GCAGCTTCAACCTCC | 219333 |
rs559038954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162505 | ATGGGGCTAATACTA[C/T]CTAACCTTTCCTAAT | 219333 |
rs559051371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159871 | ATTAGCACTGAAATG[A/G]TATAATAACTACAAC | 219333 |
rs559083703 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP12 | GRCh38.p7 | 13:27113194 | AGCCAGGGAGGCGAA[A/G]CTGCAGTGAGCCATG | 219333 |
rs559096251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27110478 | TCTGCCCCACTGAAA[C/G]AGGAGTTACCAACTT | 219333 |
rs559118223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124533 | CACTGTTCCAGTTTC[A/G]TGTTTCAAGTCATAT | 219333 |
rs559121416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106406 | GGGGCGAGACGGGGG[A/C]GGGGGCGGGCGGGGA | 219333 |
rs559167263 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27069581 | ATACAACTACCCTTT[C/G]ATCCAGCAATTCTAC | 219333 |
rs559223244 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067604 | AGGTCTGCTTATGGA[A/G]AAAATAGGTGAAGTC | 219333 |
rs559296343 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27099661 | TTTCCCTGATATCTC[C/T]TGCATTACATGGTAA | 219333 |
rs559315458 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163031 | TAACAAGTTTTAACA[A/G]CCCACTGAACTGTCC | 219333 |
rs559318556 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147899 | TTGGGAGGCTGAGGA[C/T]GGAGGATCACTGGAG | 219333 |
rs559321702 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27108965 | ATACATATGTGTGTG[A/T]GTGTGTATATACACA | 219333 |
rs559322489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155266 | TTTTGTATTTTTAGT[A/G]GAGACAGGGTTTCAC | 219333 |
rs559328044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149012 | ACATGGTGAGAACCC[A/G]TCTCCACCAAAAATA | 219333 |
rs559353377 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136018 | AGATCAAAATATTAT[A/T]TTAAACAGACCCCAA | 219333 |
rs559368522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27085185 | TTCTTTCTTTCTTTT[C/T]TTTTTGAGATGGAGT | 219333 |
rs559461271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099673 | CTCTTGCATTACATG[A/G]TAAAATTCACAATAA | 219333 |
rs559592299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142912 | ATCCTGGCCGACATG[A/G]TGAAACCCCATCTCT | 219333 |
rs559630758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136620 | AGAGTCAACTCACGT[C/T]AAATTAGAGAAGACA | 219333 |
rs559634491 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167768 | ATTTAATATAATATT[A/C]TTGTTATATGAAGAG | 219333 |
rs559705244 | snp | C/G | 3.29837e-05 | 0.00406088 | intron-variant | USP12 | GRCh38.p7 | 13:27075173 | ATTCCACTACTATGT[C/G]CCCGGAGTTGCAATT | 219333 |
rs559722115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145219 | GAGTTTCCTTCTTGA[A/G]GAATGACAGGTGGCC | 219333 |
rs559798710 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27085924 | TAATTCCAGCTACAC[C/T]AGAGGCTGAGGCAGG | 219333 |
rs559868561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27090800 | GCAACCTGTGCCTCT[A/C]CACTCAGTTAAGCAA | 219333 |
rs559888336 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172754 | CCTCTTTCTCCTTTT[A/G]TAAAATTCATATTTG | 219333 |
rs559889779 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134387 | AGACACAGAAAAAAA[A/G]AGGAGAATAAGTCAG | 219333 |
rs559906059 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | USP12 | GRCh38.p7 | 13:27083876 | TATATATATATATAT[A/T]TTTTTGAGATGAAGT | 219333 |
rs559951560 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173458 | CCCGCTAACCACCCA[A/T]ATGCCTCCTTGTCCA | 219333 |
rs559958742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27091382 | CTCAGGGGTCTTCAT[C/T]TGAAATGTTCCTTTT | 219333 |
rs560050106 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27065664 | TACAAAGATCAGCCT[C/T]GAGATCAGAAGCACA | 219333 |
rs560081592 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130744 | CTTCCCCACGACTAA[C/G/T]GTGGTTTTTTCAGTG | 219333 |
rs560085041 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27085587 | TTTCAGAAGTGAATT[A/C]ATCCAAGTAAAGGTC | 219333 |
rs560097551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119883 | GTGGTAATGACACTG[C/T]GCAGCAGATTCTGCA | 219333 |
rs560128750 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27099077 | CATCTCCACTAAAAA[C/T]AGTTCCCATAAAATG | 219333 |
rs560143008 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27123280 | CTTTCCAGACCTCAG[C/T]TTCCTCAGATGTAAA | 219333 |
rs560168637 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27074134 | GGCCGGGCGCGGTGG[C/T]TCACGCGTGTAATCC | 219333 |
rs560183922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27072902 | GAAGCAAATCTACAA[A/G]TAAGTCTGATAAATA | 219333 |
rs560214544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128316 | AACCACTCTGTCAAG[C/T]CTTCACATTTGGCTT | 219333 |
rs560221208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27114906 | GGCAGGATTGCCTGA[A/G]CCCAGGAGGTGAAGG | 219333 |
rs560224387 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130104 | CCTCAGCATCCCCAG[A/G/T]GGCGGGCACAGGACC | 219333 |
rs560240000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27094806 | AAACAACTAAATGCA[A/G]TGTCCCCCTCTAAAT | 219333 |
rs560271931 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27087359 | TACCTAAAGGTGCAA[C/T]GACCAAATAAGTAAA | 219333 |
rs560288065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27122645 | TGACAGAGTGAGACC[C/T]CATCTCAAAATAAAT | 219333 |
rs560304309 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27072479 | GTTTCTTAGGCATCT[A/G]ATTTCTGGACATTAA | 219333 |
rs560338054 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128911 | GAAAATCACTATATA[A/C]ATACAAGGTATTATT | 219333 |
rs560357997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27088036 | CTCTGTAAAACATCT[A/G]GGGAACATTCACTCA | 219333 |
rs560376459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152096 | AAACAGTCTGGTAGA[A/T]CCTCAAAAGATTAAA | 219333 |
rs560465820 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27116221 | GGAGGCTGAGGCAGG[A/G]GAATGGCGTGAACCC | 219333 |
rs560496468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144559 | CTATATATTAAAAGA[C/G]ACTAAAGATTAAGTA | 219333 |
rs560518571 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162069 | ACAACTCCTACAGTC[C/T]ACAGTATCTTAATGT | 219333 |
rs560544689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27078165 | CATATTGGGAGTTCC[A/G]CATCCACAGATTCAA | 219333 |
rs560567326 | snp | A/G | 0.000119048 | 0.00771425 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171553 | CCCGCCCGCCCGAGA[A/G]GTCCCGGCAGCCCCG | 219333 |
rs560609154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158449 | TGACAGGGATACATT[C/G]TGAGAAATTGACTGT | 219333 |
rs560618168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27118711 | GCCATCAACCAAAAT[A/G]CAACCTCAAATACTT | 219333 |
rs560630056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164505 | TACCACCTCACACAG[C/T]GGTGCTCTACATTAA | 219333 |
rs560630633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070636 | TCGGCTCACCACAAC[C/G]TCCGCCTCCCGGGTT | 219333 |
rs560641759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109200 | TTAAGCAATAATTAT[C/T]AATGGATGCTCAAAG | 219333 |
rs560652557 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102452 | TGCTCAGAACCCTCT[C/T]GTGGTTTCCCATGGC | 219333 |
rs560715785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124980 | TGTGAAATTCAGTAT[C/G]TGACTACCTGTGTTC | 219333 |
rs560732135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074293 | TAGTCTCAGCTACTC[A/G]GGAGGCAGAGGCAGG | 219333 |
rs560776695 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27076814 | AAATATGGTGGATAG[C/T]TTATTATTCCTAAAT | 219333 |
rs560824527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152396 | CATATACTCTATGAT[A/T]CCACATACCAAAGTC | 219333 |
rs560859234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27101097 | ACAAAAATACCTCCA[A/G]TGACTTGAATGCTCT | 219333 |
rs560899870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168125 | CTCCTAGCACCTACC[C/T]TTACCAGCTTTGGCC | 219333 |
rs560956211 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP12 | GRCh38.p7 | 13:27111709 | CTATGTATATTAAAA[A/C]TGTAAAGGAATGCAA | 219333 |
rs560958445 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27105427 | AAAAAGAAACAAAAA[A/C]CCTTCATTCTTGACA | 219333 |
rs560959122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160943 | CTTCCTGATGCTCTC[A/C]CTCCCGCCATCCTCC | 219333 |
rs560996005 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125500 | GCTTCCAAGATGGCC[A/G]AATAGGAACAGCTCC | 219333 |
rs561006738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149099 | TGAAATGGAAGAATC[A/G]CTTTCACCCAGAAGG | 219333 |
rs561047004 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27098177 | TTTCAGATTTCTGGA[C/T]TACGGATGCTCAACC | 219333 |
rs561129810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27082325 | GAACCCACCCCTGCT[A/G]GCTTCAAAATTTTCT | 219333 |
rs561196269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27089126 | AAAGACTAAAGAGAC[C/T]GAATGCTAAATGTAA | 219333 |
rs561214725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130932 | TTCAGCAAGCCGTGA[C/T]GCTTAAAAACAAGGG | 219333 |
rs561253803 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157409 | AAAGTGGATGTTCTA[C/G]GTATGATCTCTCCCA | 219333 |
rs561261026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109834 | GAATCGCTGGAACAC[A/G]GGAGGCTGAGGTTGC | 219333 |
rs561261091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117691 | ATATACCTGAGTGAG[C/T]GCTGGAAGAGGGATG | 219333 |
rs561281992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27096778 | GGTCAATAAAATGCA[C/T]TGAGAAAAATTACCT | 219333 |
rs561297557 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140391 | AGTTATGAAAACACA[C/T]AGTCAAAACTTTTAG | 219333 |
rs561298571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159446 | CATATAATTCTGGTG[C/T]TTTACAAGTGTTCTA | 219333 |
rs561304962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156455 | CAACGATGATCATTA[C/T]GGATCCAACTATAAT | 219333 |
rs561348051 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141483 | AATGTAAGGCTGGAG[A/G]AAGGAAGATACAAGA | 219333 |
rs561369009 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP12 | GRCh38.p7 | 13:27102795 | TGCTTCCCCACGAGG[A/G]TGTCAGGTACCTGAA | 219333 |
rs561385052 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138266 | AACATACTCCGAAAG[G/T]CTCAGGGAGCTGAGA | 219333 |
rs561413225 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147423 | CAATTCTGGATAATC[A/T]AAAAATTCTAGCTAA | 219333 |
rs561421331 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27169718 | AAATCCCTGTGTCTC[A/C]CTGTCCTAATCTGAT | 219333 |
rs561475370 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148067 | CCAAGAGGTTGAGGC[C/T]GCAGTGAGCTGTGAC | 219333 |
rs561486761 | snp | A/G | | | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162895 | AATGTCTGCTGCTAC[A/G]GAAGCAAGAAAATTC | 219333 |
rs561553783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151040 | GAACGACAAAAGAAA[A/G]AAATCAGGCCAGACG | 219333 |
rs561558769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099842 | GGACCCATTAGCCTT[C/T]AGCAAAATCCCCATG | 219333 |
rs561586770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27085760 | TGGGGAATATGTGTA[C/T]ATACACACAAAACTG | 219333 |
rs561597039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131624 | TATGTAAAAGTCTGA[A/G]GTTAGCTTCCTATGG | 219333 |
rs561633986 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27086774 | CTCTTACTTATCCAA[C/T]GGTCTTAGGTACTTT | 219333 |
rs561658877 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27121918 | AAAACAAATGTCTCA[C/T]ATGTGTCAAGAAATG | 219333 |
rs561660884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27114595 | AAATTATAGTGACAG[A/G]TAATTAAGAGTAAGC | 219333 |
rs561676351 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139384 | ACTTTGGAAGGCGGA[-/G]GCGGGAGGATCACCT | 219333 |
rs561682368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152172 | ATGTCCATAAAAAGC[C/T]TGCACCCCCAATGTT | 219333 |
rs561690638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27100703 | CCACCTCAAACAGGT[C/T]CACTAAGGCAAGGAG | 219333 |
rs561691376 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152714 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT | 219333 |
rs561695346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27107706 | AAGATATGGCTGATA[C/T]AAGATCTGCGATAAG | 219333 |
rs561753494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142442 | AAAATATGCTGTGCA[C/T]TAGATGACAGCATTG | 219333 |
rs561780561 | in-del | -/AAT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150233 | ATTATGTCAATTAAA[-/AAT]AATAAAGCAAAAAAT | 219333 |
rs561808361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151541 | AATCCCAGTGCTTTC[A/G]GAGGACTAGGCAAGA | 219333 |
rs561826476 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161563 | AAAATGTTACTAATA[A/G]GGAATTGCAGTGTTT | 219333 |
rs561870507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143678 | CATCACAGAGTGATA[A/C]AACTGCCATCATGTT | 219333 |
rs561874524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27093267 | GAGAAAATATTTGCC[A/C]AAGACCCACCTGATT | 219333 |
rs561875523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136706 | CTACCCACAAGGCAC[C/T]ACTAGGCTAAAACTT | 219333 |
rs561934774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137249 | TAAACAATAATTCTA[A/G]GTGTCATTAAAGAAG | 219333 |
rs561996636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129027 | TGCAGACTCTGACTC[A/C]CCCTAATAAAAAGCA | 219333 |
rs562026626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27092240 | AAATAAGGGGAGACA[A/G]TGCATGTACTTAGAT | 219333 |
rs562039023 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163034 | CAAGTTTTAACAACC[A/C]ACTGAACTGTCCTTG | 219333 |
rs562061666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147785 | AAATTTTAAAAAACC[A/G]TCAACCAACAATGCT | 219333 |
rs562072349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27098815 | ATTTAAATTATGCTA[C/T]AATTTTGTTAGGGAA | 219333 |
rs562073489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126948 | CCTCCATCCCAACTA[A/C]AATGCCATCTATTAC | 219333 |
rs562108617 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139864 | ACAAAGTTATGACTT[-/A]TCCTTACAGAAAGGG | 219333 |
rs562120641 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27119929 | TGCTTATTGCATGCA[C/T]TCAAGGTTTTCCTTA | 219333 |
rs562249630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27121251 | CCAAAATTCATAACC[A/G]TAACTAGGCCCTCGT | 219333 |
rs562276805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27076828 | GCTTATTATTCCTAA[A/G]TTACTTACTAGTGAA | 219333 |
rs562278535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070510 | CATGGCTTAATTTTT[C/T]TTTTTTAAAGCCAGG | 219333 |
rs562300550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27096046 | TAAAAATACTACTAA[C/T]TGATCCTGAGAAAAG | 219333 |
rs562303142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127644 | AAATCTTCAACCTGA[C/T]AGGGAAGATTTCTGG | 219333 |
rs562307170 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27072141 | GATGACACATCAAAA[C/G]TTTTTCTTAAAAAAG | 219333 |
rs562384031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27088156 | CCGGGCGCAGTGGCT[C/T]ACGCCTGTAATCCCA | 219333 |
rs562401707 | in-del | -/CAAGCA | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27079577 | CTACCCAGCCGCAGG[-/CAAGCA]CAAGCAACACCACTA | 219333 |
rs562499930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27094602 | TGTGTGCCTACAGAC[A/G]TGATGCCCCGAGAAA | 219333 |
rs562500235 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124772 | ATCCAAAGTATAAAG[A/G]TGAAACAAGTTCATC | 219333 |
rs562502069 | snp | A/G | 0.050227 | 0.150302 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156844 | CAAAAGAGAGAGAGA[A/G]AAAAAATGATTTTAT | 219333 |
rs562506178 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130224 | AGTAGCCTGGGGAAA[C/G]AGCACAGATTCTTGC | 219333 |
rs562539564 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123982 | TGAAATTACAAAGAT[A/T]CCTTTGACCTATTAT | 219333 |
rs562554256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27079538 | GACTGACATTGCCTG[C/T]AACCACCCTCAACCG | 219333 |
rs562596486 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173703 | AAAAATTAGCCAGGC[A/G]TAGCAGTGTACGCCT | 219333 |
rs562624028 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155866 | AAATGTATGACTTTC[A/G]GAATACAACTATGAA | 219333 |
rs562636746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27081408 | TTCAAGTTTGATCAT[A/G]AGATTGCAGCAATTC | 219333 |
rs562666025 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27078848 | GAACACCCTAACTAT[A/G]GACTTAATTGACATT | 219333 |
rs562763912 | in-del | -/TAA | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163221 | GCTAAACACACACTT[-/TAA]TAATCATTTTAATGT | 219333 |
rs562773243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27102172 | GATGCCAGCTGATGT[A/G]GCCCTCAGGCCCACC | 219333 |
rs562805516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118390 | TTTTAAGTTTTATAT[A/G]AAACCTTAATACCAT | 219333 |
rs562858461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27102653 | ATTTCTGATCTAACA[C/T]TACCTAATCAGGGAC | 219333 |
rs562902308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164609 | TTCCTAAATAAATGT[A/G]TATAAACTGCCACTC | 219333 |
rs562913773 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27071470 | AGACATATTTTTCTA[C/T]CATTTTATAAGGGAG | 219333 |
rs562945470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27075799 | CTTTGGGAGGCCGAG[A/G]CAGGTGGATCACCTG | 219333 |
rs562952515 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27088647 | TGACTAGCCCCAAAT[-/A]AAAACTCAGGGCACT | 219333 |
rs562965715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158012 | AATGGACCTGATTGC[A/G]CCATTAGTTTTACTG | 219333 |
rs563031270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158508 | ATAGAGTGTACTCAC[A/G]CAAACCTAGATGGTA | 219333 |
rs563118339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152995 | GAATATGTATGTCAA[C/G]TTGGAGTCTTTTTTG | 219333 |
rs563131507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106353 | TGGGGTATGTCACTA[C/T]ATCTTACTGAACTCT | 219333 |
rs563172966 | in-del | -/TA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167959 | ATGTCCTTTCTAATT[-/TA]TGTTTTTAAAAATCG | 219333 |
rs563214367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27095018 | AAATTAGCTGGGTGT[A/G]GTGGCACGTGCTCGT | 219333 |
rs563250156 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143714 | TGATAACCTGCAATA[A/T]GAAGAACACAGTATC | 219333 |
rs563255328 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134970 | GCTGAAGATATCTAT[A/G]AACAGTTCAAATAAA | 219333 |
rs563290815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161795 | GCTCAGGCAGGAGGA[C/T]AGCTTGAGCCCGGGG | 219333 |
rs563340555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149882 | CATAACAGGGTTCAC[A/G]CTCCTGAGAATCTAA | 219333 |
rs563342969 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168102 | TCAGAAGAAAAGCCC[A/G]TGGGACTCTCCTAGC | 219333 |
rs563359807 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27119741 | AAGCCCACAATTCAA[C/G]AGCTTGAAGAATGAT | 219333 |
rs563362746 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155062 | TTTTTTCTGATGTCC[A/C]CAACTTTTTTTTTTT | 219333 |
rs563400214 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP12 | GRCh38.p7 | 13:27113184 | AGCTGCAGTGAGCCA[A/G]GGAGGCGAAACTGCA | 219333 |
rs563416054 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155819 | CTAGATGCGGAAAAG[G/T]TTCAACTTAATTTGT | 219333 |
rs563447000 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27090807 | GTGCCTCTCCACTCA[G/T]TTAAGCAAATGCTTT | 219333 |
rs563477459 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156296 | ACACAAAGGATGGAA[A/G]AACATGTTAAACATC | 219333 |
rs563570499 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27115384 | TGCATAGTGCACAGA[A/G]ACATTCCCAAAGCAC | 219333 |
rs563590355 | in-del | -/AGG | | | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27065828 | ATTACTACACAGGAA[-/AGG]AGGAGGAGCAGGAGA | 219333 |
rs563615207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148115 | GACTGGGCAACAGAG[C/T]GAGACCTATCTCAAA | 219333 |
rs563627388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142861 | GCACTTTGGGAGGCC[A/G]AGGCAGGCTGATCAC | 219333 |
rs563661921 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27103800 | GAGATGAAAAAAGAA[A/G]AAAAGCCCATTTGGA | 219333 |
rs563664335 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27111125 | CAATTCTCTGAGGCC[C/T]GCCATTAGTCTTCTT | 219333 |
rs563679939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140944 | CTATTCCAATTAAAA[A/G]GATAGAAGATTCGAA | 219333 |
rs563681940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27089817 | TAGATTGTTTTTCTA[A/G]GCCCACCTCCAACAT | 219333 |
rs563684122 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141724 | AGTAGAATGCCAACT[A/G]AAACACAGAGAAGGA | 219333 |
rs563752019 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27110482 | CCCCACTGAAACAGG[A/T]GTTACCAACTTTTTG | 219333 |
rs563861223 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27097982 | GGTAACTTTATATAG[C/T]ACTTTTTTTTTTTTT | 219333 |
rs563945428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27090684 | TCACTTGCTCATGTG[A/G]ACTGGAATAGGACAG | 219333 |
rs564028884 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172632 | CAAAATAGGGAGGAT[C/T]TCAAGCCAGCAGTGA | 219333 |
rs564054293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145045 | GCATTCCAGCCTGGG[A/C]TGGACCCTGCAGCAG | 219333 |
rs564062114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27100448 | TTGCTCTCAATCACA[A/C]AAGTGCCCAAGATAC | 219333 |
rs564116462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137970 | TAGGAACCAGAAAAA[A/G]CCTAGAGCCTTCACT | 219333 |
rs564156248 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27170131 | CCATTTAATACAAAT[A/G]CTTTCCTAAAATGTA | 219333 |
rs564169330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27087311 | TGTGCATGCAGGGAG[A/C]GGGGGCAGGAAGGCA | 219333 |
rs564172361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144409 | CTGAGGCAGGATGTT[C/T]GCTTGAGCCCAGGAG | 219333 |
rs564191946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127773 | CATCTAAATTTCTCA[C/T]CTCTTCAGAAAAAAT | 219333 |
rs564222299 | in-del | -/AG | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163776 | CTGTCTTAAAAAAAA[-/AG]AAAAAAAAAGAAAAA | 219333 |
rs564251155 | in-del | -/TT | 0.0850919 | 0.187897 | intron-variant | USP12 | GRCh38.p7 | 13:27072104 | CACCAACAAAAATAC[-/TT]TTTTTTTTTTAACTA | 219333 |
rs564263839 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129232 | AACCACAGTTAAGTG[C/G]AAAGAACAAAGCAGC | 219333 |
rs564315654 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27121407 | GGCAGAATTACAAAT[A/T]CGCTCTGGAATGAGA | 219333 |
rs564323387 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129891 | ACATCCAAAACATAC[A/G]AGTGGAGTGACCAAC | 219333 |
rs564336230 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27093283 | AAGACCCACCTGATT[A/G]TGAACTAGTAGCCAA | 219333 |
rs564374353 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27091080 | CACTGTACGATGGAA[A/G]ATACAGCAACACTAC | 219333 |
rs564386062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122591 | TGGGAAGTGGAAGCT[A/G]CAGTGAGCCGGGAGT | 219333 |
rs564397659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136493 | ACAAGAATGAAAGCC[C/T]GCCTCAAATAAACAA | 219333 |
rs564400789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27085497 | TCAAATTGATTTTTG[G/T]TTTTTTACTAAGAAC | 219333 |
rs564417033 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27120123 | TTTTACTGTATGATT[G/T]TTACCATCTTTAAGA | 219333 |
rs564419012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157265 | ATCCCTTTTTGCTTG[A/G]TAAGTTTTACATACA | 219333 |
rs564435348 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27120546 | GTAATTCCAGCTATT[C/T]AGGAGGCTGAGGCTG | 219333 |
rs564460473 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117445 | ATTTATGATTGCAGC[C/T]GACAGCAGTCTAGAT | 219333 |
rs564460934 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27092391 | TTTACATGGAGAGGC[A/C]AAAGACCCAGAATAG | 219333 |
rs564551746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27077030 | CTCCTATTAGAGTTC[C/T]TTTACATTGTAAAAA | 219333 |
rs564591355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124235 | AAGAAAACAATTCAA[C/T]CTGGAATTAATGTAA | 219333 |
rs564625290 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27115494 | TATTTAGAGTCCACC[A/G]ATCTGTTCAATATAA | 219333 |
rs564634584 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27078073 | TTCTATTTAAATTTA[A/T]TTTTTTAATGACATT | 219333 |
rs564636545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070008 | AAAATGAGTGTATAC[A/G]TCCAGCAAAAGGCTT | 219333 |
rs564649686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117889 | TGAGCACCATGGTGG[A/G]GGATGACACACAAGC | 219333 |
rs564672832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070576 | TTTTTTTTTTTGAGA[C/T]GGAGTTCACTCTTAT | 219333 |
rs564718967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163745 | TGTAGGAGACAGCCT[A/G]AGCAATAGAGCAAGA | 219333 |
rs564731703 | in-del | -/AGGTTCTT | | | intron-variant | USP12 | GRCh38.p7 | 13:27106143 | GTAAAGTTTTCTATC[-/AGGTTCTT]AGGTACATCCAAATT | 219333 |
rs564733540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27077901 | TCTTGATCACTGTCA[C/T]TGTTTTAAAAAAAAA | 219333 |
rs564735262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27118580 | AGAAGTCCCTGACAT[A/G]TGTTGAAAATAACCA | 219333 |
rs564736904 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27121705 | TCTCTACTAAAAATA[A/C]AAAAAATTAGGTGGG | 219333 |
rs564765393 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | USP12 | GRCh38.p7 | 13:27114780 | TTTTTAAAAAAAAAA[A/G]AAAAACAAACTTGAG | 219333 |
rs564769986 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102802 | CCACGAGGGTGTCAG[G/T]TACCTGAAGGCATAT | 219333 |
rs564770240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27081450 | CAGGATCCTCTTCTA[A/G]TTCTTGTTCTCTTGC | 219333 |
rs564804061 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP12 | GRCh38.p7 | 13:27107882 | AAAAAGTCAGGAAAC[A/G]ACAGGTGCTGGAGAG | 219333 |
rs564814881 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155137 | CCCAGACTGGAGTGC[A/G]GTGGCGCGATCTCGG | 219333 |
rs564850014 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130676 | GGTATTATTAAATCA[A/G]TCGTATCAACGGTAT | 219333 |
rs564881710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167862 | TTTTTTCAGTAGTAA[A/G]GATAAATTGCACTGA | 219333 |
rs564888669 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173350 | ATCTGTGTGCCCGTC[C/T]TGATAAATAGCTGTG | 219333 |
rs564902810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27072430 | CTAAAAATGAAATGA[A/G]AGATGAAGGGCTGAA | 219333 |
rs564954212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073695 | AAAGCTAAGATGTGA[A/G]AAGGTAATATTACAT | 219333 |
rs565057598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104731 | CTAGATATGATCCAG[G/T]CTTACCTCAATTCAC | 219333 |
rs565171316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116870 | AGCAACAGGCTCTAC[C/T]ATCTAGCCTAGGTGT | 219333 |
rs565210819 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159210 | CATTTTTCTTTAAGA[A/G]TATATACAGTTAAAC | 219333 |
rs565225662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163805 | AAAAAAAAAGAAAAG[A/C]AGCTACAGGTAAGAC | 219333 |
rs565236420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165690 | CTTAATGGTACTGGC[A/G]AAGAAAAAAGTGTCA | 219333 |
rs565255290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143001 | GGGAGGCTGAGGCAG[A/G]AGAATCGCTTGAACT | 219333 |
rs565259416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109744 | CATGGTGAAACCCCG[C/T]CTCTACTAAAAATAC | 219333 |
rs565293449 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158727 | GGCACTTTGTTATGG[C/T]AGCCCTAGGAAACTA | 219333 |
rs565368279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27098398 | CAAAACAAGAAAAAA[A/T]ATTTTAAAAACTGGC | 219333 |
rs565374505 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164171 | TAAAATCAAAGGCAA[C/G]AGTACTCTAACTCTA | 219333 |
rs565435611 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141141 | CTGCCCCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 219333 |
rs565463151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099114 | TGGCTTCCTATTTGG[A/G]CATATATATTTAAGT | 219333 |
rs565463245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27090974 | GTATTTTATAGACAG[C/T]TGAAGGGAGTTCCAA | 219333 |
rs565465078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139926 | CAATAAACAAGTGAT[A/G]GTAAAAAAGATGTTC | 219333 |
rs565485204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154245 | TCTGATGTAATCTTA[A/G]CATCCTAAAATATAT | 219333 |
rs565494171 | snp | A/G | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27091840 | AGACACCAGCTTCCT[A/G]CCACCTGAGACATTA | 219333 |
rs565511294 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138911 | GAAAGTTTGCACCAG[C/T]TGTCATGGCATAATT | 219333 |
rs565540988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139237 | CTGAGTAATTAATTT[C/G]TATAATGCTGATATA | 219333 |
rs565629953 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155360 | TGCTGGGATCACAGG[C/T]GTGAGCCACTGCACC | 219333 |
rs565637303 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27078253 | ACAAAAATAATACCA[A/T]TTAAAAAAATACAGT | 219333 |
rs565664779 | snp | C/T | 8.42524e-05 | 0.00648992 | intron-variant | USP12 | GRCh38.p7 | 13:27105683 | AATTATGGCACACTA[C/T]ATTTAACCTTCCTAG | 219333 |
rs565700107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149300 | ACTTAATAGCGAAAA[C/T]ACTGGATGCTTTTCC | 219333 |
rs565758802 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150251 | AATAAAGCAAAAAAT[G/T]GTATTTATATATGCT | 219333 |
rs565764703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142161 | ACACGCAATGACAGT[A/G]AAGACAGTGAAAAGC | 219333 |
rs565865794 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127822 | ACTGCGCAAGTAACT[A/G]CAAATTTAAATTTAC | 219333 |
rs565909512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168434 | TGCCCATGACGGACC[A/G]CCCGGATTAGCCACC | 219333 |
rs565933448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127264 | TGGCATTGCACCATT[C/G]TGGTACACATGGCAG | 219333 |
rs565949067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27076141 | CAATCTATATGATGC[A/G]GGTACAGACTGACAA | 219333 |
rs565984966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27081650 | GAGGGGTTTCAATTT[A/G]CTTTGCTCAGATCCA | 219333 |
rs565990333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27169862 | CGCCTCTAGCACTTA[C/G]TGGCTGCTAAGTGTA | 219333 |
rs566012395 | in-del | -/ACT | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165993 | AATAATCATTTATAA[-/ACT]ACTAAAGGATCAGAA | 219333 |
rs566027064 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068753 | CATCTTTGTCTTCCC[A/G]ACACTGGATTATCTA | 219333 |
rs566036419 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27089266 | TTTGGATGGATGTGC[A/G]CACATAGGAAAACGT | 219333 |
rs566131559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132848 | CTGGCAAGACCATGA[A/C]TCTAGCCTTATCCTA | 219333 |
rs566170021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109898 | GCCTGGGCGACACAG[C/T]GAGACTCTGTCTCCA | 219333 |
rs566175818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171244 | AGGCCGGGCGCGCCT[C/G]GGCCCTCGTCCCCGC | 219333 |
rs566176305 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161102 | CCTCCTAACGCAAAC[A/T]TCAAAGTCCCAGCTA | 219333 |
rs566238891 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27172011 | GCGCGGCCAGGCGGC[A/G]CAGCCCCGCCCACCC | 219333 |
rs566239914 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27071278 | TGCTTCTTTTTTATA[A/C]CCCTTACCTATTCTT | 219333 |
rs566242460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155271 | TATTTTTAGTAGAGA[C/T]AGGGTTTCACCATGT | 219333 |
rs566289798 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27081280 | TAAGGTTATGTAATA[C/T]TCTAAATCCTTTGTT | 219333 |
rs566361056 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161899 | AAAATAAAAAAAAAT[A/T]AAAAAAAATTAAAAA | 219333 |
rs566365715 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165781 | TAACCTCCAGTTTTA[A/G]AGAAAGAAAAATGTA | 219333 |
rs566371343 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27112774 | CAGATAGAGTATAGG[A/C]ACCAGTCTCATCCAT | 219333 |
rs566379340 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27107693 | CTCGGACACCTTGAA[A/G]ATATGGCTGATACAA | 219333 |
rs566415276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129321 | CTCTTACCATTTTCC[A/C]GCTATAAAACTGTGG | 219333 |
rs566438239 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27085994 | AACATAGCAAGAGCC[C/T]GTCTATAAAAAATAA | 219333 |
rs566470874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128554 | GGTGGGCAAGATGTG[C/T]TTTTTCAGCATCTTC | 219333 |
rs566481884 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159431 | TCCATTTGCATCAGG[A/C]ATATAATTCTGGTGT | 219333 |
rs566510307 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | USP12 | GRCh38.p7 | 13:27091752 | ACACCCACATTTAAA[G/T]AATGGAAAAAGAGAA | 219333 |
rs566511265 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27120608 | GCCTAGGCAACAAGA[A/G]CAAAACTCCATCTAA | 219333 |
rs566522079 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27086935 | TACCAAAAACACTTT[A/C]CTTCCTAGGAAATGT | 219333 |
rs566528301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27121780 | GCAGGAGAATGGCGC[A/G]AACCTGGGAGGCAGA | 219333 |
rs566572722 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27070349 | ACAAGGGGGCCTGCT[A/G]CGGTGTTGAAAATGA | 219333 |
rs566595703 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27113823 | CTATGGCCATCAGAT[A/G]AGGAGAAACTGAATG | 219333 |
rs566596584 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27114896 | GGGAGGCTAAGGCAG[G/T]ATTGCCTGAGCCCAG | 219333 |
rs566618340 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156889 | GGAAGAAGCATCTAC[A/G]CCTACATTAGTAACA | 219333 |
rs566622400 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27095260 | GTAATCGTAGAAAAA[A/G]GAAAAACGAATTAAT | 219333 |
rs566634129 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068874 | TCTATACATACTGAA[C/T]CAGGCAAATTTATGC | 219333 |
rs566653425 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158730 | ACTTTGTTATGGCAG[C/T]CCTAGGAAACTAATA | 219333 |
rs566667204 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27120701 | TGAGCACATGACATA[C/T]ACAAATGGAAGAAGA | 219333 |
rs566726671 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162696 | TAGGTTTCTTATTGA[G/T]CAATATTTTGTTTTT | 219333 |
rs566727403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27108920 | TACTCGGGCTTGGGC[A/G]ACAGAATGAGACTTT | 219333 |
rs566743222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143237 | AACTAAACACTGAAT[A/C]AATAAAAATCTATCA | 219333 |
rs566743805 | in-del | -/TT | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140137 | TAATCCCCAAAATAG[-/TT]TTTTTTCCCTACGTG | 219333 |
rs566752353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152717 | GGAGGCCGAGGCGGG[C/T]GGATCACGAGGTCAG | 219333 |
rs566807262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143860 | AAGGAAATGTTCAGA[C/T]AAATCCAGATAGTGT | 219333 |
rs566844519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170421 | ATAAATAGGGCCAGT[C/G]AGGCATGAAACACAA | 219333 |
rs566877685 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | USP12 | GRCh38.p7 | 13:27093255 | GTCACGGACTGGGAG[-/A]AAATATTTGCCAAAG | 219333 |
rs566901482 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126357 | TGGAGTGGACCTCCA[G/T]CAAACTCCAACAGAC | 219333 |
rs566947057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27108063 | ACTACAAATCATGCT[A/G]CTATAAAGACACATG | 219333 |
rs566955057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156718 | CCCAGGTACTCAGGA[C/G]GCTAAGGCAGGAAGA | 219333 |
rs566985626 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27100525 | TCCTCCTCATCCACT[C/G]ATGGCCTGATTCAGT | 219333 |
rs567105326 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27092965 | ACTTTAGGAGGCCAA[A/G]GTGGGTGGATCACTT | 219333 |
rs567195908 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP12 | GRCh38.p7 | 13:27093588 | AGAAGGAAAAATCGT[A/C]CAGCCACTGTGGAAG | 219333 |
rs567209989 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141432 | ATCTTGGTTTCTAAA[A/T]ACCATTCTCCACTAA | 219333 |
rs567242947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159776 | AGCTAAAATTACAGA[C/T]GTCACATTCAACTTT | 219333 |
rs567243072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167329 | ATTGACCTTCCTTTT[G/T]CTTTCTTGGAGTTTT | 219333 |
rs567244325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154479 | AAAAATTCTCCTTCC[A/G]TTACTTCCAAAACTA | 219333 |
rs567271230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132972 | GGTGATGGCAACACA[G/T]CCATGCTCCTACTAT | 219333 |
rs567394814 | in-del | -/T | 0.251296 | 0.249997 | intron-variant | USP12 | GRCh38.p7 | 13:27070504 | TGTTACATGGCTTAA[-/T]TTTTTTTTTTTTAAA | 219333 |
rs567411632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155167 | GCTCATTGCAACCTC[C/T]GCCTCCAAGGTTCAA | 219333 |
rs567425571 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27090418 | TGTGAGAGTTCATGA[C/T]TTTCCAAAGTCTTTG | 219333 |
rs567446500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104786 | TTAAAGGCAGGATTA[C/T]GCAATAGGGTATTTA | 219333 |
rs567478700 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148442 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 219333 |
rs567480979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27097657 | CAAGCTCCCTGTTCC[A/G]TAATTCCTCATCTGA | 219333 |
rs567515326 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153131 | AAGGTCAGGAGTTCA[A/C]GACTAGCCTGGCCAA | 219333 |
rs567544260 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27080592 | AGAGACTTGAGAGAG[A/G]AAAGATGAGAAGGCA | 219333 |
rs567581364 | snp | A/T | 6.65413e-05 | 0.00576769 | intron-variant | USP12 | GRCh38.p7 | 13:27090001 | AATTTATTTTGTAGA[A/T]ACCAGGAAATCATGT | 219333 |
rs567683423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145737 | CTTCTTTATCAACAA[A/G]AGTCTGTAACTCTAT | 219333 |
rs567725682 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101770 | TTGGAGAAAAAGAAT[C/T]GTTTGAAATAAACAT | 219333 |
rs567772123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130933 | TCAGCAAGCCGTGAC[A/G]CTTAAAAACAAGGGT | 219333 |
rs567793381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130442 | ATACAAATGGATGAC[A/T]GCAAGCCTCAAAAAA | 219333 |
rs567804655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139496 | GGCTGTGCACCTGTG[A/G]TCCCGGCTACTCAGG | 219333 |
rs567806059 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160700 | TCAGCTTTAAACCTC[C/T]AGGTCCATCAAACAA | 219333 |
rs567807901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27080321 | TGATACTACACAAGT[C/T]ACCATTACTGGAACT | 219333 |
rs567814763 | in-del | -/AAAAGA | 0.00597247 | 0.0543191 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132439 | AAGGCAAAAAAAAAG[-/AAAAGA]AAAAGAAAAAGCAAA | 219333 |
rs567815057 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136089 | ACAATAAAGTAAACC[A/G]CTTTCCATGTTCTGT | 219333 |
rs567833040 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123647 | ATAAGTCTCATGAGA[G/T]CTGATGATTTTACAA | 219333 |
rs567864755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27076434 | TGGCTCAGCTCAAAT[C/G]TCACACCCTCTGGCA | 219333 |
rs567868023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27085214 | GTCTCGCTCTGTTGC[C/G]CAGGCTGGAGTGCAG | 219333 |
rs567927754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158463 | TCTGAGAAATTGACT[A/G]TTAAGCAATTTCATC | 219333 |
rs567981218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124351 | CATTTTGAAAAGTTA[C/T]ATTCAGTATATACTA | 219333 |
rs568009658 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150333 | TTCAAAATGATTTAA[A/G]TAAGTAGGAATCAAT | 219333 |
rs568028351 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124650 | AGGTGGGAAAAGCAC[A/G]TGACCTGGTAAAATA | 219333 |
rs568041684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099234 | ACTTCTAGGTTTGTT[G/T]GGTACTGAAATGTTA | 219333 |
rs568054914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27114047 | ATTCTGAAGGGAAAG[C/T]ACATTTCTTTTTTTG | 219333 |
rs568084995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142634 | TGCATTATTCTTGCA[A/C]TTTTTCTGTAAATTC | 219333 |
rs568122673 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133816 | ATTCAGAAAAATGTC[C/G]TAATTTTATTCTAAT | 219333 |
rs568149515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143023 | GCTTGAACTGGGGAG[A/G]CGGAGGTTGCAGTGA | 219333 |
rs568193364 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151501 | AACTCTTACACCAGG[G/T]CCAGGCAGGGTGGCT | 219333 |
rs568202246 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27113149 | TAAAGGCAGGAGGAC[A/G]GCTTGAGCCAAGAAG | 219333 |
rs568223142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169219 | GATTACAAAAATGCC[A/C]TGAAACTGTATGAAG | 219333 |
rs568276997 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170424 | AATAGGGCCAGTGAG[C/G]CATGAAACACAAGAT | 219333 |
rs568284830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162022 | ACTTTGAAATGACTA[C/G]GCTTTGTCAAAGGTA | 219333 |
rs568321349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070270 | TCATAATGATAGAAG[C/T]CCAAATAGCAGGCTC | 219333 |
rs568350785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162585 | CAAAATAAAATTAAT[A/G]CTTTTGAAATACCTC | 219333 |
rs568354009 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163328 | AGACCCGCTTTCACG[A/C]CAAACCACCTACAGA | 219333 |
rs568372477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125227 | TAAGTTGAAATTTTT[A/T]AAATTTTATATACAA | 219333 |
rs568400654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074598 | ATGTTCCAAATACAA[C/G]TTTTGATTATGTGAT | 219333 |
rs568415606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082519 | GTGGGTTCACTAGAG[C/T]AGCTCTTTTAATTCT | 219333 |
rs568513081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125987 | TTGAACTGGGCGGAG[C/G]CCACCACAGCTCAGC | 219333 |
rs568515323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27083240 | ACAATATAATAATGA[A/C]AAAGTTTGAAATAGT | 219333 |
rs568527873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27075581 | ACATCTTAATATGAC[C/T]CCACCCTACCCATCA | 219333 |
rs568582354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119599 | AGAAAATTAAAAGAT[G/T]ATGTGATTTCTAAAA | 219333 |
rs568614448 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068944 | TTCCGATTCTTTCTA[C/T]TGCACCCCCAAGGAA | 219333 |
rs568616645 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27104791 | GGCAGGATTACGCAA[C/T]AGGGTATTTAATAAT | 219333 |
rs568627884 | in-del | -/TGA | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27109113 | GGGGCACTAAACAGT[-/TGA]TGAAGGAAGTTTCTG | 219333 |
rs568657943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149523 | GAATAAACGAGTTCA[C/G]CAAGGTTGCGGGTTC | 219333 |
rs568676661 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27071744 | TAACTATGACTATGA[C/T]TGCCCCTGCATCTCA | 219333 |
rs568727163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159585 | ATGTACCCAAATATC[C/G]TAACTCTCTTTAACA | 219333 |
rs568728972 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153222 | CCTGTAATACCAGCT[A/T]CTTGGGAGGCTGAGG | 219333 |
rs568736455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113263 | CCCTTTCTCAAAACA[A/C]AAACAAAAACAAACA | 219333 |
rs568776623 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106430 | GCGGGGAAATAAACC[A/T]ACTTTATAAAGTAAA | 219333 |
rs568785610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27087499 | AAGAGATCAATAGAC[A/G]TAGAAGAGAAATAAA | 219333 |
rs568790564 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153742 | AAGAACCACTCATAC[C/G]TAACAGTTCACCTAG | 219333 |
rs568801908 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27172076 | CGGGGAACTCCGGTC[C/G]GTCCCCACCCCGCGC | 219333 |
rs568802364 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067874 | CTTACTGATGCATGG[A/G]AAAACGTCCAAAAAA | 219333 |
rs568832980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122740 | TAATATCAGATAGTA[C/T]TTTTTAGCCAATATT | 219333 |
rs568846648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122400 | CAGCCATGTGGAACT[A/G]TAAGTCCAACTAAAA | 219333 |
rs568866335 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118245 | CTAGGCTGAAAAGGG[G/T]ACTGATAAAGGCACA | 219333 |
rs568866597 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132178 | TCAGGGATTATAACA[A/T]TTACATTAGCTTCTA | 219333 |
rs568886787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27107497 | AAAAATAAAAGCCTT[A/G]TAAACTTCAGTTAGA | 219333 |
rs568974012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27108211 | TGCAGCCATAAAAAA[C/T]GATGAGTTCATGTCC | 219333 |
rs568981356 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP12 | GRCh38.p7 | 13:27099387 | ATGGGGGTCTCGCTA[C/T]GTTGTCCAGGCTGAT | 219333 |
rs568993741 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27091327 | TGGTGTTTCTCAAAA[C/T]CAATTTTGTATTCCT | 219333 |
rs569028591 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118193 | CTGGGAAGCCCAGAA[C/T]CTTTGTTAGACATGC | 219333 |
rs569028847 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27120278 | CACATTTGAGAAGTA[C/T]GACCCTATCAAAACT | 219333 |
rs569030894 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27089593 | CTTCACCAAGAAAAA[A/T]GTTTACATCATCAGG | 219333 |
rs569051126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109457 | AATACCACAAAGAAG[A/G]AAAAGGCCAAGTTTG | 219333 |
rs569111199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145774 | AAATTTTGTTATCAA[C/T]AGAGAAAATGAGAAA | 219333 |
rs569120120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070767 | CATATTGGTCAGGCT[A/G]GTCTCAAACTCCCGA | 219333 |
rs569131052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136922 | AGAGGTGTTTTTTGC[A/G]TTAACTAAAGCATGA | 219333 |
rs569139245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109891 | CACTCCAGCCTGGGC[A/G]ACACAGTGAGACTCT | 219333 |
rs569164786 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP12 | GRCh38.p7 | 13:27115428 | CATCACTTCAACCGC[C/T]TTCCTCAAATCCATG | 219333 |
rs569227065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156838 | AAAAAACAAAAGAGA[A/G]AGAGAGAAAAAATGA | 219333 |
rs569230043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163871 | AGGGTCTCCTATCAA[C/G]CCAGATACCTCCAGG | 219333 |
rs569257845 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138440 | GAGAGATGGTGTATC[A/C]CCTGTATCGCCCTCC | 219333 |
rs569268049 | in-del | -/TGTCATTATG | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27110284 | TAAATTGTATAATCA[-/TGTCATTATG]TGTCACAATCATTGC | 219333 |
rs569290707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157519 | GATTTTTAACAACAT[A/G]TACATGCCTTTTTTT | 219333 |
rs569312796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152032 | GGATGCAGAGAAATG[G/T]GAACAGCCATACACT | 219333 |
rs569360911 | in-del | -/AAG | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142800 | TATCGTGACACAAAA[-/AAG]AAGTGGAAGAGGCCA | 219333 |
rs569372695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144825 | AGCACTTTGGGAGGT[C/T]GAAACAGGCAGATCC | 219333 |
rs569376292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104845 | CTGCTTGTGAGCGTC[C/T]ACTTAATAGGTAACA | 219333 |
rs569413547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27097745 | GCTTAGAATACAACA[A/G]TAGGTTTTGTATTCT | 219333 |
rs569420772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27093648 | TATACTCTTACCATA[C/T]AATCCAGTGATCCTG | 219333 |
rs569504375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27098283 | TATGGCAAAGTCAAC[A/G]TAAATGAAGACAAGT | 219333 |
rs569577741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133914 | AGGCAATAGGATCAC[A/G]TGAGCCCAGGAACTT | 219333 |
rs569585551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27087060 | ACACAGACATCTGTA[C/G]AGGCAGGAGAGGGGG | 219333 |
rs569598499 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067507 | TTGTCAAAATACTTT[C/T]TGATATTTTGTACAA | 219333 |
rs569604100 | in-del | -/A | 0.170408 | 0.236992 | intron-variant | USP12 | GRCh38.p7 | 13:27094743 | GGGAGGCATATTCTC[-/A]AAAAAAAAAAAGACC | 219333 |
rs569610415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27111595 | CTAATGCCTTCTTCT[C/G]CAAACCTTAACAAAC | 219333 |
rs569626150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148460 | GCGGGCAGATCACGA[A/G]GTCAGGAGTTCGAGA | 219333 |
rs569626421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154771 | GCTAAAATCAAACGA[C/T]CTTGAGAGAGTATCC | 219333 |
rs569634319 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166475 | AAAGTCTAGAATCAA[A/G]TAAGGCAACAAGAAA | 219333 |
rs569639994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126135 | TTCTCCCAGCATGGT[A/G]TTTCGAGCTCTGATA | 219333 |
rs569734106 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27075004 | AATAAAAACAATATA[-/T]TTTAACATATAAAAT | 219333 |
rs569743301 | snp | C/T | 1.66322e-05 | 0.00288371 | intron-variant | USP12 | GRCh38.p7 | 13:27090168 | GCTTATCTGTAAAAA[C/T]AGTGAATTGTCTTTG | 219333 |
rs569863339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27090937 | TATGCAAATATACGT[A/C]AACCAAGGTACTGTG | 219333 |
rs569930070 | in-del | -/AGG | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27169036 | TTCACCCGGCATACC[-/AGG]AGGAGGCAGGAAGGA | 219333 |
rs569939155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27096383 | ATCAAGAATTATCTA[C/T]ATAATCCAGATAATC | 219333 |
rs569981961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27088540 | CTCGCTGTGCCTAAA[C/T]TGTTTGAACAAACAA | 219333 |
rs569992121 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP12 | GRCh38.p7 | 13:27074395 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAGAAAAA | 219333 |
rs570032487 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27112341 | CCCAGGCTGGGGTGC[A/G]GTGGTATGATCATGG | 219333 |
rs570035661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147567 | AAACAAAGTGTATGT[C/G]ATAAACACAAAAACA | 219333 |
rs570073545 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27074246 | TCTACTAAAAATACA[A/G]AAAATTAGCCGGGCG | 219333 |
rs570075614 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27086693 | TTTTGCTCACAGATG[G/T]GCCTTCCTCCATATA | 219333 |
rs570128276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131087 | AGTAAAATTCATTTT[G/T]TAAAATAAGCACAGA | 219333 |
rs570151881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27089186 | ATAAAGGACATTACC[A/G]GTACATCCTGTGATA | 219333 |
rs570188641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123697 | CGCTCTCTTGCCTGC[C/T]GCCATGTAAGACATG | 219333 |
rs570188816 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132022 | GTGCTTCTACTGGTT[C/G]TACATCTAAATCTTT | 219333 |
rs570204030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118101 | GCCTCTTCAGCTACA[C/T]TGGGCATATGGTCAA | 219333 |
rs570232271 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066837 | TACAACCTCACGATG[C/T]TTTCTTCATGGGTCA | 219333 |
rs570267800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27078361 | ATGCTATGCCATTTT[A/G]TATCAGGGACTTGAG | 219333 |
rs570276240 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124476 | ATAGCCAAACTATTA[A/G]TTTCCACACAACTTT | 219333 |
rs570292241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27110892 | TGAACAACTTCCACC[A/G]AGCAGGGAGATGAAA | 219333 |
rs570321369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168266 | AACAACTTCTCCGTT[A/G]TCTGGTCCCCCTCCC | 219333 |
rs570337938 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171719 | GCCGCCCGCTCGCAC[C/T]GCAGCCCGCGGGCGG | 219333 |
rs570338467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125117 | AAAACAGATCAGACA[C/T]ACATCTTTATTAGGA | 219333 |
rs570382513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27093494 | CACTACACACTTATT[A/G]GAATGGCCAAAATCC | 219333 |
rs570393891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27071532 | ATAAAACAATGCATA[C/T]AGAATTATTTCTAAG | 219333 |
rs570401396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27112897 | CACACTTCATTTGGA[A/G]ACTACTAGTTTTAAC | 219333 |
rs570416972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136751 | ATGGTCCATATGCTC[A/G]GGGAGCATTCAGTAT | 219333 |
rs570429567 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136229 | GACCCTTGGCGGGGC[A/G]CGGTGCTCACGCCTG | 219333 |
rs570438768 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144374 | GTGGTGCATACCTGT[A/T]ATATTAGCTACTCAA | 219333 |
rs570451455 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148707 | AATATAAATAATAAT[A/C]ACAGCACAAAAGAGG | 219333 |
rs570456370 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27085338 | GATGTGTGCCACCAC[C/G]CCTGGCTAATTTTTG | 219333 |
rs570501011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127048 | TCTGGGGGTTCTGCA[A/C]TGATCTGCAGTCATC | 219333 |
rs570551287 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148048 | GTGGGAGAACCACTT[A/G]GGCCCAAGAGGTTGA | 219333 |
rs570587364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128515 | TCTGAACTCCGTAAC[C/T]GGCACCTTACCTAAG | 219333 |
rs570589725 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171070 | CCCCGGCCGAGACCC[C/T]TCCTTCCTGCCCGCC | 219333 |
rs570599703 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142108 | GCCTGGGTGACAGAG[C/T]GAGACTCTGTCTCAA | 219333 |
rs570604138 | in-del | -/ATT | | | intron-variant | USP12 | GRCh38.p7 | 13:27096143 | CTTACCTGACTTATT[-/ATT]TCACAAATATTTCAA | 219333 |
rs570645919 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27121704 | GTCTCTACTAAAAAT[A/C]CAAAAAATTAGGTGG | 219333 |
rs570710498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122263 | CCCCCATACTGTTCT[C/T]GTGGTAGTGAATACG | 219333 |
rs570711191 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170489 | GTTGCAAAGAACAAC[C/T]TTTTTCGGTGATGAC | 219333 |
rs570712842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27084232 | CAAATTCCTGTCTGG[A/G]TGTGGTGGCTCATGC | 219333 |
rs570730135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150470 | AGAGAAAAACATACC[A/G]TGTTCACAGACTGGA | 219333 |
rs570736061 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27108248 | GGGACATGGATGAAA[C/T]TGGAAATCATCATTC | 219333 |
rs570743409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119645 | CATTCTATCGTTTCC[A/G]ATCACTTTCATGAAT | 219333 |
rs570749333 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157536 | ACATGCCTTTTTTTA[A/T]AAAAAATATAAGTTT | 219333 |
rs570784948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151115 | GGGCAGATCACTTGA[A/G]GCCAAGAGTTCAAGA | 219333 |
rs570812739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27075692 | CTGTATTTTTCAAAC[A/G]CACGTCTCTTATAAT | 219333 |
rs570819746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134472 | ACTTTGCCATGCCCA[C/T]ATAAAAGGTAAGCTG | 219333 |
rs570833826 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27088717 | GGGAAGAATTAATAG[-/T]TCTTTTGTGACTCCA | 219333 |
rs570935958 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27113333 | ATGTTGAAAAGGAAC[C/T]GTTTTTGAAGAAGCA | 219333 |
rs570936669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27069521 | ACACAGCTGGCAGGG[C/T]ACACCAAAAAAATGT | 219333 |
rs571062482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153799 | GGTATTCTTTCCTGT[A/C]TTCCTTATCATCTCT | 219333 |
rs571090918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099297 | CTTAAAAATAACATA[C/G]AGCTTTCCATACAAA | 219333 |
rs571091254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27107294 | CGCACCACTGCACTC[C/T]GGCTTGGATGACAAA | 219333 |
rs571181115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166762 | AAGTGCCTAAGATTA[C/G]AATAAACCACCTCTT | 219333 |
rs571188001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147742 | CAGTGGGGTAATATA[C/T]TCAAAGCGCTCAAAG | 219333 |
rs571233387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27072679 | AGGAGAGACCTCATC[C/T]AGCAAGACAGGAGGT | 219333 |
rs571265633 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109982 | TACCACTGCATTGGA[A/T]GATATTAAGAAATTG | 219333 |
rs571307422 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27073161 | TTCCAGAGCGGAGGG[A/G]CAGGAAGGCATGAGG | 219333 |
rs571313821 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165966 | GCTCCTAAAATGATG[-/A]AAAATGATACCAATA | 219333 |
rs571346006 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27065836 | ACAGGAAAGGAGGAG[A/G]AGCAGGAGAAACAGT | 219333 |
rs571374371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160395 | TCCTTGTTCAGCAGG[A/G]TCCCCCGTGGAGGAG | 219333 |
rs571385154 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27089376 | TAAAAAAGCTTTCTT[A/G]GTCTATTCATGCAAC | 219333 |
rs571446000 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27121782 | AGGAGAATGGCGCGA[A/G]CCTGGGAGGCAGAGC | 219333 |
rs571490213 | in-del | -/AT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148388 | AAACTATATATATAT[-/AT]TATAGGCCAGGCATG | 219333 |
rs571706447 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27089648 | ACTGTACTGGTTTAT[A/G]ATGATTAAATAATCG | 219333 |
rs571718302 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164167 | AAAATAAAATCAAAG[G/T]CAACAGTACTCTAAC | 219333 |
rs571745173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153051 | AAGCTTAGTGTCCTG[A/G]CCGGGCATGGTGGCT | 219333 |
rs571747584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133587 | TGAGCCAATATCGCG[C/G]CACTGCGCTCCAGCC | 219333 |
rs571752923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138471 | AGAAAACACCTTTTA[C/T]AGAGCAAGCTTTTAG | 219333 |
rs571788446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130887 | TAGCTAATTCTTGAA[A/G]GCAACAACATTTAAA | 219333 |
rs571797547 | in-del | -/TA | 0.00835141 | 0.0640778 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137796 | TGTCACTTCTGTGAC[-/TA]TGTGACATAATGTAA | 219333 |
rs571815857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130369 | GTAAGACAGAAACTT[C/T]AGTGACCACACACAA | 219333 |
rs571832249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27080252 | TGTGCCAACAGGTGG[C/T]TGCAGATGCTGACTA | 219333 |
rs571877528 | in-del | -/ATC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159460 | TTTTACAAGTGTTCT[-/ATC]ATCATTAAATTTCAT | 219333 |
rs571899283 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27104956 | TTATCTAAATTCCAT[G/T]TGAATTTTTGAGGCA | 219333 |
rs571905651 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140732 | AGCAATTTTAGATAT[A/T]ATAAATTCAAAGATT | 219333 |
rs571914968 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156868 | ATTTTATGGTTGTCT[C/T]TAGGGGGAAGAAGCA | 219333 |
rs571981869 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173083 | CATAGTGATTCCATT[A/G]TAAGCTTGCTTGGGG | 219333 |
rs571983339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082147 | TATGACAGTCCTAAA[C/T]ACCCTCTTTTTCCAA | 219333 |
rs572007910 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156221 | CAACTCCTGCAAGGA[-/A]AAAAAAAAAAAAAAT | 219333 |
rs572028818 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148669 | ACAGAGACTCAAAAA[A/C]AAAAAATTATATATA | 219333 |
rs572048323 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102368 | GTCTCCTGCCTCTAC[A/T]CTCATGCTGCCCAGG | 219333 |
rs572051567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27113140 | CTCAGGAGGTAAAGG[C/G]AGGAGGACGGCTTGA | 219333 |
rs572089380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133218 | GTTCAATAAACTTAA[C/T]GCAAACACCACACTC | 219333 |
rs572092669 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141621 | TGGGTATCAAAATCA[A/G]TAATAATAATGAGTC | 219333 |
rs572165972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074858 | GCTGAACATACGCAA[C/T]TAAACTCAGAAGTGA | 219333 |
rs572191581 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066222 | CTTCAAGAACCTTAA[A/T]TGCTTTACAGACATT | 219333 |
rs572218109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167603 | TTAACACAGCAAAAT[C/T]AGATAAGTAAAACAA | 219333 |
rs572276063 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066959 | TTTACTTAGATCCAG[A/C]TGCATTAAGAAGAAA | 219333 |
rs572312412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162169 | TGTATTTATAGTACA[A/G]AGGACGTTCACATGT | 219333 |
rs572317838 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140850 | GACAATGATTCTCCA[A/G]CCAAAATGACACACT | 219333 |
rs572354831 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069044 | AGGAGCTGGTATCTC[C/T]GATTTCACCTCCTTG | 219333 |
rs572356244 | in-del | -/ATA | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170526 | TTATGATCCCTACAT[-/ATA]ATAAGCTCATGAGGA | 219333 |
rs572377946 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167271 | CGTCTCAAAAAAAAA[-/T]ATAAAATAAATAAAT | 219333 |
rs572400962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142699 | GAGGGGCTTCCACTG[A/G]CAAAATCGAGACTAA | 219333 |
rs572476127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165223 | TGTTCCCAGATAAAA[A/G]AAATAAATTATTCTA | 219333 |
rs572476550 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123931 | CTTGTCCTTTTCACA[C/T]CCAGAAATCACCATC | 219333 |
rs572529003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117668 | GAAGAATGTATATTA[A/C]ATATACTATATACCT | 219333 |
rs572550115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163504 | CTTTCACATATAATT[A/G]CCATTACTTATACCA | 219333 |
rs572575355 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160859 | TGTGACACAGGTAAA[A/C/T]GTATCATGGTGGTTT | 219333 |
rs572581584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27110944 | TATACCAGAAATATT[A/G]TGATAATGAGGATTG | 219333 |
rs572617258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118225 | TCTTCAATTTCCTGA[C/T]AGCTCTAGGCTGAAA | 219333 |
rs572754045 | in-del | -/A/AA/AAA | 0.264632 | 0.249571 | intron-variant | USP12 | GRCh38.p7 | 13:27076029 | GCAAGGCTCCGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 219333 |
rs572759804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27069901 | GTGGTGAGCCGAGAT[C/T]GCACCCTTGCACTCC | 219333 |
rs572774639 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067726 | TAGCAAAAGGACTTT[A/G]GAAAATGACAATTTT | 219333 |
rs572840183 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152427 | CAAAGCAGATAATTA[C/T]ATAAACACATAAAGT | 219333 |
rs572846652 | in-del | -/A/AAAA | 0.177182 | 0.23916 | intron-variant | USP12 | GRCh38.p7 | 13:27109912 | TGAGACTCTGTCTCC[-/A/AAAA]AAAAAAAAAAAAAAG | 219333 |
rs572902245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156917 | ACAGCATGATCCGGC[A/G]GCAAAAGCACTAGAC | 219333 |
rs572920716 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157627 | ATTACTGAAACATTA[A/T]ATCATGTAAGTAATT | 219333 |
rs572931431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27114402 | TTGCTGACTATCTAA[C/T]AGCTGGCCTGTAAGT | 219333 |
rs572995111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150539 | ATCTACAGGCTCCAT[A/G]AGATCTCCATCAGAA | 219333 |
rs573020378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27100642 | AATTCAAGAACCTTT[A/C]TCTCTCACTCACCCA | 219333 |
rs573031665 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154660 | AAAAAAAAACGTGGA[C/T]GCATTGTGGTAGTAG | 219333 |
rs573058499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142786 | AATAAATAAAAATCT[A/G]TCGTGACACAAAAAA | 219333 |
rs573160568 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155644 | GGAGTAGTAAATATA[A/T]AACCCTGAGGCGGAA | 219333 |
rs573398212 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27093556 | GGAGAAACAAGAACT[A/C]TCATTCACTGCTGGT | 219333 |
rs573416825 | in-del | -/TTTTTTTTTTTT | 0.114387 | 0.210022 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141013 | TCAGTGTGAAGTCAC[-/TTTTTTTTTTTT]TTTTTTTTTTGAGAT | 219333 |
rs573421429 | in-del | -/TGAGCTGAGAT | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27095098 | AAGTCGAGGCTACAG[-/TGAGCTGAGAT]TGGGCCACTGCACTC | 219333 |
rs573424229 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124410 | ACCAAGAAATTAAAA[A/G]TGATGAAAACATAAA | 219333 |
rs573435149 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27121742 | GGCAGGCACCTGTAG[C/T]CCCAGCTACTCAGGA | 219333 |
rs573465255 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127449 | ATATTGTACAACCAG[A/T]TATCAAGCTCTAATA | 219333 |
rs573505441 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27076706 | ATACTCCTCACAATT[G/T]AAAGAAGTGATATAT | 219333 |
rs573531561 | in-del | -/AAAT | 0.00636936 | 0.0560724 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155676 | ATATTAAAAAATGGA[-/AAAT]AAAAGAAAAACTACT | 219333 |
rs573537770 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27102521 | TGACTTTATCTTCAT[C/T]TTATTCCACTCTTGC | 219333 |
rs573552575 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154644 | ACATTTTTTAAAGTT[-/A]AAAAAAAAACGTGGA | 219333 |
rs573590872 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154975 | AGGCAAAGAAACAGT[C/T]CCTCCTGCAGCTCCA | 219333 |
rs573614844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153956 | CTAATTATGGCAGTC[A/G]TTTAATAACTGCAAA | 219333 |
rs573622512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27095973 | ATAACAAATAACTTT[C/T]GCATCTAAAACTTTT | 219333 |
rs573684469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27096530 | GTGCTTGGCAATATA[C/T]AACTCTACCATAGAA | 219333 |
rs573781750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27088082 | CCAAGAACAGTAATG[G/T]GAGGTTCAGAAAAGG | 219333 |
rs573840093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123966 | TGAAATAATAATAGG[C/T]TGAAATTACAAAGAT | 219333 |
rs573866167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073541 | GGGAGAGTGGGGAGG[A/G]GACCCCTCCCCAATG | 219333 |
rs573869887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27088690 | AGCTTCCTGTGTTGT[A/C]ACAATTCAATGTGGG | 219333 |
rs573887096 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068950 | TTCTTTCTACTGCAC[A/C]CCCAAGGAATTCAAA | 219333 |
rs573950854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109276 | ACCTAAACACCCCAG[C/T]GATTTCAGCATTGCT | 219333 |
rs574001344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128987 | TTAGTTTAATAGTAA[C/T]GGAGTTCATACTCCA | 219333 |
rs574033508 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129712 | TAATAGCAAATAAAA[A/G]TAAATGTATGCATAA | 219333 |
rs574057662 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076038 | CGTCTCAAAAAAAAA[-/T]AAAAAAAAAGAGTGG | 219333 |
rs574074204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27079458 | CCAGTAGCCCAAGGG[A/G]GAGTCCTTCCCAGAG | 219333 |
rs574083888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082921 | GCTCACCGCAACCTC[C/T]GCCTCCCAGGTTCAA | 219333 |
rs574106094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137878 | AGGAGCAAGCTGCCG[C/T]GCTGAGAGGACTTAT | 219333 |
rs574113996 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27072222 | GTCTTGTGTGTTATG[A/G]GGAGAGGGTCAGAAA | 219333 |
rs574120614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27083618 | CACTGCTATCTTTCC[C/T]GAACTGCACTATTTA | 219333 |
rs574129007 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27096943 | ACATTTTAGAAGAGA[A/T]ACAGATATGACTACA | 219333 |
rs574147056 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27073810 | TTACATTTTCTAGAA[A/G]AGAAAACTGAAGGCT | 219333 |
rs574186094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27122820 | GAAACGTGGCCAGGC[A/G]CGGTGGCTCATGTCT | 219333 |
rs574201381 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172365 | TCTGCACAGTTAAGA[C/T]AACCCGGGTATGCGT | 219333 |
rs574218398 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139548 | TTGAACCTGGGAGGC[A/G]GAGGCTGCAGTGAGC | 219333 |
rs574223016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27072758 | ATGGGCTTGAAGGGT[A/C]ATACTTAAGTCAACA | 219333 |
rs574233738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27096711 | TGACTCCACCATGCC[A/G]CACACAAAGTAATGC | 219333 |
rs574243975 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27092625 | ACAGAGAAAGAATTG[C/T]CTTTTAAACAAATGA | 219333 |
rs574260240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159028 | TATCCCAACTCTTTC[C/T]AGCAATTACTTCTTG | 219333 |
rs574268216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165460 | TAATTAGTAGTGCCA[A/G]TGAATACTTTTTACC | 219333 |
rs574305482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27113166 | CTTGAGCCAAGAAGG[C/T]GAAGCTGCAGTGAGC | 219333 |
rs574327882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166316 | TGGAAAGGAATTATA[C/T]AAAGTATACAAATGC | 219333 |
rs574370508 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126889 | AGATGTTCAGAACAA[C/T]GCCTGGCACAACAGG | 219333 |
rs574375757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074906 | CCCTCTATACACACA[C/T]CCCAAAAAAGGAAAA | 219333 |
rs574429021 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106713 | CCATTTATTTTTTTT[A/T]AAAAAATGAGGAAGG | 219333 |
rs574444900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142319 | CAAGTCGATAAAGAC[A/G]AAAAAAGGCGGAAGA | 219333 |
rs574446766 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133485 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGCGGGC | 219333 |
rs574459931 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167762 | TTCATTATTTAATAT[A/G]ATATTCTTGTTATAT | 219333 |
rs574460500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126740 | ATTCTAAAATAGCAG[C/G]ACTACTGTAGAGTTA | 219333 |
rs574479263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169449 | AATTTTCTTTAAAGA[A/G]TAAGACTGCAAATTA | 219333 |
rs574501711 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27119717 | AGTCTAAGACAACCA[A/C]TATATGCCAAGCCCA | 219333 |
rs574502256 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27084879 | TTTAGGGTCTTCTGT[G/T]ATTCCATGTGGATTT | 219333 |
rs574509627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134223 | ACTAAAGAAGCTCTC[C/T]CTATAGGGTTACTAA | 219333 |
rs574514762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27170034 | CTAATTATCGCATTC[C/T]TTTTGAAATTGACTA | 219333 |
rs574521445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160869 | GTAAACGTATCATGG[C/T]GGTTTGCTGCACAGC | 219333 |
rs574528284 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069129 | GATCGGAAGGGCTTG[C/T]CAATCCATCGTCTTT | 219333 |
rs574562345 | in-del | -/T | 0.0158469 | 0.0875917 | intron-variant | USP12 | GRCh38.p7 | 13:27102794 | TGCTTCCCCACGAGG[-/T]GTGTCAGGTACCTGA | 219333 |
rs574601023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161168 | TGAGTCTCTTCATTA[A/C]GCAAATTAAACAAAC | 219333 |
rs574652884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162228 | TATTATTCCATTTCA[A/T]AACTGAAACCAGTTA | 219333 |
rs574655991 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27109196 | TGGATTAAGCAATAA[C/T]TATCAATGGATGCTC | 219333 |
rs574694197 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066374 | GAAGAGCCAGGACAT[A/G]AGCGCTTTAGCCTCC | 219333 |
rs574711882 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27065680 | GAGATCAGAAGCACA[A/C]TGGGAGAATGAAGGA | 219333 |
rs574714648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155747 | AATTATAGTTCAGAT[A/G]CAAAAATCTGTTAGA | 219333 |
rs574726860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074095 | TTTGCTCCCTCCAGA[C/T]TGTCCTTAAAAATTC | 219333 |
rs574875803 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27104553 | TCTAATAAAGTACAT[A/T]CGTTTAGCTTTCATT | 219333 |
rs574888209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148103 | TACTGCACTCCAGAC[C/T]GGGCAACAGAGCGAG | 219333 |
rs574947985 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155279 | GTAGAGACAGGGTTT[C/T]ACCATGTTGGCCAAG | 219333 |
rs575011552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148743 | TGAAATGGGCTAACA[C/T]AAAATAGCATATCAA | 219333 |
rs575028353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27111717 | ATTAAAAATGTAAAG[C/G]AATGCAATTAAGAAA | 219333 |
rs575045666 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27097907 | AATGAGATATTTTGG[G/T]GATGTGACTCAAATC | 219333 |
rs575120987 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131077 | TCAAAATGCAGTAAA[-/C]ATTCATTTTTTAAAA | 219333 |
rs575200823 | snp | C/T | 0.0001182 | 0.00768675 | intron-variant | USP12 | GRCh38.p7 | 13:27071027 | AAGTGAAAAGCAACA[C/T]ATGCATACAACTTTC | 219333 |
rs575290637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152175 | TCCATAAAAAGCTTG[C/T]ACCCCCAATGTTTAC | 219333 |
rs575309942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135672 | GTATGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 219333 |
rs575347630 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144269 | TTGGGAGACCAAGGT[A/G]GAAGCATCACTTCAG | 219333 |
rs575372178 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136466 | TCATGCCACTGCACT[C/G]CAGTCTGGGCAACAA | 219333 |
rs575449674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27108976 | TGTGTGTGTGTATAT[A/C]CACATAATGACATTT | 219333 |
rs575452223 | in-del | -/A | 0.0192894 | 0.0962945 | intron-variant | USP12 | GRCh38.p7 | 13:27103413 | AAATGCTTTTCTATT[-/A]AAAAAATGGCTTTTC | 219333 |
rs575452551 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | USP12 | GRCh38.p7 | 13:27087285 | TGTGTGTGTGTGTGC[A/G]CGCACGCTCGTGTGC | 219333 |
rs575488255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27101847 | AACTAAAATTTCCTC[A/G]CTTGAGGGAGACCAA | 219333 |
rs575518389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128714 | AAAGCAAGGATCCCT[C/G]GATTGCCACCCTGCG | 219333 |
rs575546417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150609 | ATTCATATGGAGGTC[A/G]GACCCAGTGGCTCAC | 219333 |
rs575585632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137951 | ACTGAGGGCAGCTGC[C/T]AACTAGGAACCAGAA | 219333 |
rs575593760 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27113710 | AAACAGGGCTGGACG[C/T]TTGGTACAGTCTAGG | 219333 |
rs575609822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142789 | AAATAAAAATCTATC[A/G]TGACACAAAAAAGAA | 219333 |
rs575650926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129839 | AATGGTGGGGAAGTA[A/G]AAAAGAACTGGCTGC | 219333 |
rs575655714 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27093098 | CTACTAGGGAGGCTG[A/T]CACAAGAGAACCACT | 219333 |
rs575661066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27092360 | TTTGTGGATATCGAC[A/G]AACTTGATTCTAAAG | 219333 |
rs575697652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27097083 | ACCAAACTGGACAAT[A/C]TTATAAATGGCAATC | 219333 |
rs575711834 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131386 | CTACTCTGCCTACCT[C/T]GGGGTTACAGAAATC | 219333 |
rs575715978 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27105644 | ATGTTATCAGGCATA[C/T]AGATGATGCTCAGTA | 219333 |
rs575801015 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135660 | GCAAAGGTTGCAGTA[C/T]GCCGAGATTGCGCCA | 219333 |
rs575813853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27084953 | TTGATAGGGACTGCA[C/G]TGAATCTCTAGGTTG | 219333 |
rs575835113 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170663 | CCAGCGGGCATTAGC[A/T]CTTTTCCCTTACAGT | 219333 |
rs575835386 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133105 | TTTTTCTACTAGCTG[G/T]TGTCTCTCTAATCCT | 219333 |
rs575851151 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171302 | CGGGGACTCCCGGAG[G/T]CCGGTGCCCGCCCGA | 219333 |
rs575873507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27121877 | AAAAAAAAAATTAAA[C/T]ACCAGAATTAACAGA | 219333 |
rs575883892 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173442 | TTAGACCTGCCTCCA[C/T]CCCGCTAACCACCCA | 219333 |
rs575901170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27085479 | AGCCACCGCATCTGG[A/C]CGTCAAATTGATTTT | 219333 |
rs575910255 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27070527 | TTTTTAAAGCCAGGT[C/T]TGTTGTTGAAAGCTT | 219333 |
rs575945309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27096635 | AACATGAAAATGGGA[C/T]GAGACAGAGTACAGT | 219333 |
rs575966272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139809 | AAACATTTTCTTATA[C/T]GGCTTATGTGTGCCA | 219333 |
rs575973854 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133626 | AGCAAGACTCTGTCT[-/C]AAAAAAAAAAAAAAA | 219333 |
rs575987743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27088809 | CGTCCCTGTAATAAA[G/T]CTTAGCTGTGAGCAC | 219333 |
rs576019378 | in-del | -/CT | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137841 | TAGCAGACTTGCTCC[-/CT]GACTCCCTCATTGGC | 219333 |
rs576059004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27080397 | AAAGGTAGGGCCTTC[A/C]TCTCACAAACAGGAA | 219333 |
rs576064156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140636 | TATAAGTAACAAAAC[G/T]GAAGTCTTCTCTGTA | 219333 |
rs576080896 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133262 | GACATCTTTCTGTTA[C/T]TTCTATAAAAATTTT | 219333 |
rs576105758 | snp | C/G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162010 | ACTCATTTTCAAACT[C/G/T]TGAAATGACTACGCT | 219333 |
rs576113827 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130250 | CTTGCTTTTGTTTCT[A/G]TCCCCTTAGGCTGCA | 219333 |
rs576145117 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27072809 | TCTAGGCTGGGCACC[A/G]GGGACAGAGAAGGAG | 219333 |
rs576172452 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27110529 | CCAACCCCTCTCCAG[A/C]TGAGGACCTGAGACC | 219333 |
rs576184433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27073471 | GTTAAAAAGGGAAAG[C/G]GTCAAGAGACTTAAG | 219333 |
rs576185845 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27082623 | CTTTCAACGTGCCCT[A/G]TTCATTAAGCTTAAT | 219333 |
rs576225061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27081430 | CAGCAATTCAGTCAG[A/T]TCGTCAGGATCCTCT | 219333 |
rs576279795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159701 | TGTGAAATGCCTAGC[A/G]ATAGCATCACCAAGT | 219333 |
rs576295247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27081840 | CTTGGGTGATCACAT[A/G]TATTGTCAATAAGCA | 219333 |
rs576305921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27111147 | AGTCTTCTTTTATTT[A/G]CTTTCATCAATCCCA | 219333 |
rs576334769 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27119085 | AAGGCAGCTGGTGGC[A/G]CCTGGCACACAAGCA | 219333 |
rs576355300 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145038 | CACCACTGCATTCCA[A/G]CCTGGGCTGGACCCT | 219333 |
rs576365733 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141991 | GTGGTACATGATGGC[A/G]TGTGCCTGCAGTCCC | 219333 |
rs576385199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27075847 | CCAGCCTGGCTAACA[C/T]GGTGAAACCCTGTCT | 219333 |
rs576403589 | in-del | -/AAAGTAAGAACCACTCATACCT | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153721 | GACGTATCTTCCTTA[-/AAAGTAAGAACCACTCATACCT]AAAGTAAGAACCACT | 219333 |
rs576423269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27122966 | AGGCCTGGTGGCAGG[C/T]GCCTAGTCCCAGCTA | 219333 |
rs576424205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27074745 | AGCAAAATTGGCTAA[C/T]AAGAAATGATAAATA | 219333 |
rs576459849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167154 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 219333 |
rs576462138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166466 | ACTTGGTCAAAAGTC[C/T]AGAATCAAATAAGGC | 219333 |
rs576475444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27076559 | ATGGTTCTTTTCTTC[C/T]AGGCCCTGAACTCTT | 219333 |
rs576476037 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27111316 | AAAAATTATCTTTCA[A/G]GAGTAGAGCCTTCAT | 219333 |
rs576509181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116807 | TTATTCCTGTGTTAC[A/G]ATTGCCTAGAAAATA | 219333 |
rs576512655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27069790 | CCATCTCTATTAAAA[A/C]TACAAAATTAGCTAG | 219333 |
rs576517887 | in-del | -/G | 0.00874735 | 0.0655527 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165539 | CACAGTGATTACCAT[-/G]GGCCAGGTACTAGTC | 219333 |
rs576566828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117481 | ATTGTTAGGGAAATA[C/G]ATACATAAAATGTGA | 219333 |
rs576585722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27070414 | GAGTGTGTGAGTATG[C/G]CCATGTGTGTGTGAC | 219333 |
rs576664590 | in-del | -/CCGCCCGGG | 0.153665 | 0.230694 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171448 | GCCGTCCAACCGCCC[-/CCGCCCGGG]CCGCCCGGGCCGCCC | 219333 |
rs576672257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159180 | AACTACCATTTCTAA[A/G]GTAATCAGATATCAC | 219333 |
rs576722677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27084728 | GTTTTATTTCTGGGT[C/G]ATTTTGTTCCACTGG | 219333 |
rs576735632 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153459 | TCTAGTTTCAAATAG[G/T]TTCTATGAAATCTAG | 219333 |
rs576737358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159847 | ATGGCAAGAACATCA[C/T]GGTAGGCTATTAGCA | 219333 |
rs576750784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169479 | ACTTTGAGATATTCA[C/G]CACTATTTGGGGGTA | 219333 |
rs576796414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154156 | AGCCTGAGGCCTTCT[C/T]TCTAAACCTCCAAGA | 219333 |
rs576810024 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27070551 | AAAGCTTTCCCTTGT[C/T]TTATTCTTTTTTTTT | 219333 |
rs576853631 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155284 | GACAGGGTTTCACCA[C/T]GTTGGCCAAGATGGT | 219333 |
rs576911652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127426 | TTGCTAAGTCTGAGA[A/G]AAATGAAATATTGTA | 219333 |
rs576919255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148874 | TAGAAAAGAATTCCT[C/G]TCTGAATACAATAAA | 219333 |
rs576926313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163432 | TTTTGCAAAGTTCAA[C/T]TCTCTTCTAAGAAGC | 219333 |
rs576936256 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27120623 | GCAAAACTCCATCTA[-/A]AAAAAAAAAAAAAAG | 219333 |
rs576949998 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27114110 | AAGACAGGAAAAGCA[C/T]ATTTCACAGTACCCT | 219333 |
rs576951100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27106792 | TGGAGAGATGGATAA[A/C]AATGAGACTTCTCTG | 219333 |
rs576975608 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139531 | TAAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 219333 |
rs576979488 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139765 | TGCTAACATGTACTC[A/G]CCTAGACTGATTCAC | 219333 |
rs576980045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149641 | GGGGGTGGGAGGAGT[A/G]GCCAAGGGGTGGTTA | 219333 |
rs576988417 | snp | A/G | | | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27169083 | TATACTGAATGCAGA[A/G]CTTGGTACTCCAGAT | 219333 |
rs577006399 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27106153 | CTATCAGGTTCTTAG[C/G]TACATCCAAATTAAA | 219333 |
rs577024993 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167520 | ATGTAATAGAAGATT[C/T]CTTATTTTTGAGGTT | 219333 |
rs577044971 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136412 | CTGAAGCAGGAGAAT[C/T]GCTTGAACCGGGGAG | 219333 |
rs577059173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27121125 | AAGGGTTTCTCTTCA[A/G]TGCATAAGGGAACCA | 219333 |
rs577094711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27106698 | ATGTATGTCCATAGA[C/T]CATTTATTTTTTTTA | 219333 |
rs577120670 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118144 | ACTCAGAATCCCACA[C/T]CTGCTGCTTCCTTTC | 219333 |
rs577138164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156896 | GCATCTACACCTACA[G/T]TAGTAACAGCATGAT | 219333 |
rs577154441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27112051 | TTAGGAAATGCCTGC[C/T]TTGAGAGCCCCACAG | 219333 |
rs577194219 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162030 | ATGACTACGCTTTGT[A/C]AAAGGTAACTTGTGA | 219333 |
rs577206115 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27114687 | GTAACAGAAAACAGG[G/T]TGTCATTAAAGCACT | 219333 |
rs577241296 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27112988 | CCTGTAATCCCAGCA[A/C]TTTGGGAGGCTGAGG | 219333 |
rs577254054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152872 | GCGTGAACCTGGGAG[A/G]CGGAGCTTGCAGTGA | 219333 |
rs577261755 | in-del | -/AC | 0.00914312 | 0.0669923 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131924 | CAAGAAGAGAAATTG[-/AC]ACACACACACTACCT | 219333 |
rs577283970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27115696 | ATTTTCCCAAAGTTT[C/T]AAAAACGTGTAATTA | 219333 |
rs577331693 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143022 | CGCTTGAACTGGGGA[A/G]GCGGAGGTTGCAGTG | 219333 |
rs577386564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27105298 | TTTTTAGGTTTTGAT[C/T]TTTCACGGCTAAAAT | 219333 |
rs577426837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27098034 | CTTGTTGCCCAGGAT[A/G]GAGTGCAACTTCATA | 219333 |
rs577447070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142706 | TTCCACTGGCAAAAT[C/T]GAGACTAATTTGAAC | 219333 |
rs577507864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135435 | GGGTCTATGGAGGCC[A/G]GGCATGCTGGCTCAC | 219333 |
rs577537863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158407 | TGTTAGGACGATAAA[C/T]TTCTGTTACAGGCAT | 219333 |
rs577538386 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173445 | GACCTGCCTCCATCC[C/T]GCTAACCACCCATAT | 219333 |
rs577550005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27109109 | TTCAGGGGCACTAAA[A/C]AGTTGATGAAGGAAG | 219333 |
rs577602579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158838 | TCATGGGAAATTAAA[A/G]TGCACACAAGAGTTT | 219333 |
rs577654148 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126832 | GCAAAAAAGGGCAAA[C/G]AAGACTTGCAACATG | 219333 |
rs577664075 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156591 | GGGAAGCCAAGACAG[G/T]CGGATCACCTGAGGT | 219333 |
rs577685160 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27098869 | AACAGTTCCATTGAA[C/T]TAACATGGCAAAACT | 219333 |
rs577782875 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138723 | TACAATTTTTTTCGT[A/G]TTTTCAGTTTGAAAG | 219333 |
rs577819768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129581 | ATGTTGTGGAGCACG[C/T]CTGTAGTCCCAGCTG | 219333 |
rs577836271 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27122027 | AAAGTTGGAAAAGCT[A/G]AAGTAAAAACTCAAT | 219333 |
rs577841935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130679 | ATTATTAAATCAATC[A/G]TATCAACGGTATCAC | 219333 |
rs577883208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27122429 | AACTCTTTTTCTTCA[C/T]GGTCTTGGGTACATC | 219333 |
rs577887399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27088609 | CTGGAATTTGGGGGC[A/G]TGGTAGGCAGAGGGT | 219333 |
rs578017725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137033 | ATGGTTAAAGCAAAA[C/T]ACATGATTAACTGCC | 219333 |
rs578025902 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27079974 | ATGTGAGAAAGACAC[C/T]AAGGTGACTCAGTGA | 219333 |
rs578036276 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152062 | TGTTGGCAGGAACAT[A/T]AAATGGTCCATCTCT | 219333 |
rs578157379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164481 | TAAGCCAAGGAACAG[A/G]GAGGGCTATACCACC | 219333 |
rs578164558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27115517 | CAATATAACTTACTG[C/T]GTTACCTATTTTATC | 219333 |
rs578195915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165350 | AGGGGTATATACTAC[C/T]AATAAACTAACGTTT | 219333 |
rs578206894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171510 | TAGGCCCCGCGAGCG[A/G]CCACTGGGAGAGGCG | 219333 |
rs578237003 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076391 | CCTTTGTACTCCTAC[C/T]TCACCTAAAAATCTA | 219333 |
rs745349812 | snp | C/T | 3.31581e-05 | 0.00407161 | intron-variant | USP12 | GRCh38.p7 | 13:27105722 | TAATACAGTGGGAAG[C/T]AGAATTACCATTTTC | 219333 |
rs745402131 | snp | A/G | 4.9163e-05 | 0.00495773 | intron-variant | USP12 | GRCh38.p7 | 13:27105961 | TGCAACAGAAAAAAA[A/G]AAGTTTTGTTAAATT | 219333 |
rs745430533 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166041 | GAGACAAGCATATAA[A/G]GAATATCTATTAAAG | 219333 |
rs745440488 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27122902 | ATTGAGACCATCCTG[G/T]CTAACATGGTGAAAC | 219333 |
rs745441220 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27094813 | TAAATGCAATGTCCC[C/T]CTCTAAATTGGATTC | 219333 |
rs745518259 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141259 | ACCTCAGGTGATCTG[C/T]CCACCTCAGCCTCCC | 219333 |
rs745523342 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163399 | ATCCCTCCATGTCCA[-/C]ATAATAAAGGCCATT | 219333 |
rs745526498 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27107039 | CAACAACAAAAAATC[C/T]ACTGGCCAGACGCAG | 219333 |
rs745551103 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27073301 | CCAGGGCTGTGAGGA[A/G]AGTCAATAAACATCT | 219333 |
rs745602281 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146400 | AAGCCAGACTCTGTC[C/T]CAAAAAAAAGCACCT | 219333 |
rs745642897 | snp | C/T | 1.66161e-05 | 0.00288232 | intron-variant | USP12 | GRCh38.p7 | 13:27090077 | CTAAATAATTCTACA[C/T]ATACCTTAAGCAGTG | 219333 |
rs745656259 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27082765 | TTAGGGAATAAAGAG[A/G]CCTGAGAGAGAGGTA | 219333 |
rs745690203 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158604 | ATATGACTGTACTGG[A/G]TCCTGTAGGTAACTG | 219333 |
rs745690458 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27107323 | AAGTGAGACTCTGTC[C/T]CAAAAACAAACAAAC | 219333 |
rs745699459 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145163 | CTTTCCTTCCAAATC[A/G]CAGGTCTCCTCAACT | 219333 |
rs745736729 | in-del | -/TTCTC | | | intron-variant | USP12 | GRCh38.p7 | 13:27120998 | CTAGTGACCTTTAAA[-/TTCTC]TTCTAACAGCTGAAT | 219333 |
rs745743555 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170904 | CTCAGAGGAGAAAAT[A/G]GAGAGAATTTCAACA | 219333 |
rs745761242 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27096069 | GAGAAAAGGGCAAAA[-/C]CTATCCTTATATATT | 219333 |
rs745774591 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27086707 | GGGCCTTCCTCCATA[C/T]AGTCAGTAAAGTCTG | 219333 |
rs745831854 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151200 | GCTGGGCATGGTAGC[A/G]CGCAATTGTAATCCC | 219333 |
rs745837345 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27085225 | TTGCCCAGGCTGGAG[C/T]GCAGTGGCGCCATCT | 219333 |
rs745853055 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27100139 | AACCTTGCGTGGTTC[C/T]ACCAATTGGAAAAGT | 219333 |
rs745896191 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136447 | AGGTTGCAGGGAACC[A/C]AGATCATGCCACTGC | 219333 |
rs745909498 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151201 | CTGGGCATGGTAGCG[C/T]GCAATTGTAATCCCA | 219333 |
rs745931226 | snp | C/T | 1.7741e-05 | 0.00297829 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117845 | GGTCCCCGACGACCA[C/T]GTGAAAGGGAGGGGG | 219333 |
rs745963259 | in-del | -/TTTCTT | | | intron-variant | USP12 | GRCh38.p7 | 13:27085177 | TTCTTTCTTTCTTTC[-/TTTCTT]TTTTTTTTGAGATGG | 219333 |
rs745974084 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27087962 | TTTACAATCTCAAAA[C/T]GCTTCCACATAAAAT | 219333 |
rs746028379 | snp | A/C | 1.64969e-05 | 0.00287196 | intron-variant | USP12 | GRCh38.p7 | 13:27075167 | CTAGGAATTCCACTA[A/C]TATGTCCCCGGAGTT | 219333 |
rs746061873 | snp | C/G | 4.94964e-05 | 0.00497451 | synonymous-codon | USP12 | GRCh38.p7 | 13:27075292 | TAAAGGAAAAACTAC[C/G]CGGTAAGAGAGTTTT | 219333 |
rs746091466 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137194 | CATTTTGAACAAAGG[A/G]TTGTCCAAGGAAGCC | 219333 |
rs746096248 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156859 | GAAAAAATGATTTTA[A/T]GGTTGTCTTTAGGGG | 219333 |
rs746132185 | in-del | -/ATGTGTGTGT | | | intron-variant | USP12 | GRCh38.p7 | 13:27087251 | ATATAGTGGGGAGGG[-/ATGTGTGTGT]GTGTGTGTGTGTGTG | 219333 |
rs746175178 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160234 | CAACTAAGACAATGA[G/T]ACAAATATCCAAGCA | 219333 |
rs746192587 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27110695 | TACACTTCAATGAAC[A/C]CTACCCAGGGGTTAA | 219333 |
rs746205485 | in-del | -/AT | 2.72002e-05 | 0.00368773 | intron-variant | USP12 | GRCh38.p7 | 13:27095590 | ATACAAAATTGTATG[-/AT]ATATACTTACAGTTT | 219333 |
rs746214540 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27080593 | GAGACTTGAGAGAGG[A/C]AAGATGAGAAGGCAA | 219333 |
rs746225899 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128116 | GAAGATTCGGATTTA[C/T]CTTAAGTCTTTTAAC | 219333 |
rs746258512 | snp | A/G | 4.4482e-05 | 0.00471583 | intron-variant | USP12 | GRCh38.p7 | 13:27075407 | TTAAAAATAAAAATG[A/G]AAACAAAATTTCATA | 219333 |
rs746306332 | snp | C/T | 1.64825e-05 | 0.00287071 | missense, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105800 | TTTTCTTCTGAGTGG[C/T]TATGCTATGGAAGAG | 219333 |
rs746345738 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161298 | ACTAAGATAATCACA[C/T]ACAAAGCAGAATAAA | 219333 |
rs746394983 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129665 | GAACTATGACCTGGG[C/T]GACAGAGTGAGACCC | 219333 |
rs746396275 | in-del | -/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128663 | TCTTGATAATTTCTA[-/T]TATCTATTCCACCAA | 219333 |
rs746405356 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27114386 | TTGTTATCTAAGAAT[G/T]TTGCTGACTATCTAA | 219333 |
rs746458891 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156770 | GAGGTTGCAGTGAGC[C/T]GAAATCACACCACTG | 219333 |
rs746487327 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27108922 | CTCGGGCTTGGGCGA[C/T]AGAATGAGACTTTCT | 219333 |
rs746502822 | in-del | -/CTTTTTAT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165857 | ATGTCTGATTCTATG[-/CTTTTTAT]CTTTTTATGTTATCT | 219333 |
rs746522298 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105761 | ATCTTGTGATGAACT[C/T]CTTAGGGGGTATTAC | 219333 |
rs746664715 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27095913 | AAAAGAATATCTAGT[A/T]TTGGATCAGAACTAA | 219333 |
rs746670085 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143252 | AAATAAAAATCTATC[A/G]TGACACAAAAAAGAA | 219333 |
rs746717237 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27076358 | TATGCCTTTAAATGC[A/C]ATTTCTCCCTGAGAG | 219333 |
rs746766841 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155174 | GCAACCTCCGCCTCC[A/C]AGGTTCAAGCAATTC | 219333 |
rs746779403 | in-del | -/ACAC/ACACAC | | | intron-variant | USP12 | GRCh38.p7 | 13:27086288 | TATATAATTACACAC[-/ACAC/ACACAC]ACACACACACACACA | 219333 |
rs746797007 | snp | C/T | 2.40683e-05 | 0.00346894 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | USP12, USP12-AS2 | GRCh38.p7 | 13:27171613 | ACAGATGGAGGCGAA[C/T]TTGGAGACTGTCATT | 219333 |
rs746803170 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27101265 | AGTTTTAAAAGCGTC[A/G]ACCAGGACTGTATAA | 219333 |
rs746878300 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27089539 | AGAAACTGGGGGTGT[-/G]GGGGATGGGCAATGG | 219333 |
rs746885659 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27107198 | GGCATGATGACACAT[G/T]CCTGTGATTCCAACT | 219333 |
rs746888587 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133075 | CTTATTAATTATTCT[A/C]TCTCCTGCTGTAACT | 219333 |
rs746954333 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167500 | ATTCCTTTGACCAAA[C/T]ATTTATGTAATAGAA | 219333 |
rs746968776 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135825 | TACTGCCAGAAGCTA[C/G]CTAGGGAGGGGAGAA | 219333 |
rs746972988 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27072606 | ACCCCTTCAGTACAA[C/T]AGATAACTACTCCAA | 219333 |
rs747046837 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133693 | TAAATCAATCTGATC[A/G]GAAACTCTCAGCCCA | 219333 |
rs747069829 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27091201 | TAAGGAAAACACATC[A/T]ATTTTGTAGAAAAGT | 219333 |
rs747089388 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139290 | TTTTCCTACAGCTTA[C/T]GCTACATACTAGCAT | 219333 |
rs747114302 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27077389 | GTAAGATTAGGAGGA[-/G]GAAAGAGAATGAACA | 219333 |
rs747157676 | snp | A/G | 0.000106453 | 0.00729487 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117767 | AGAAACAAGGACCTC[A/G]CACAGACAATCATAG | 219333 |
rs747174729 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27111409 | AAACAAAAAAACATT[C/G]CTTTAGTGCTGAAAT | 219333 |
rs747198520 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27078544 | AGTTATAATTTAAAA[C/G]TATTCAAAAAAGAAA | 219333 |
rs747240454 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158056 | CCCTAATAAAGGTAC[A/G]TTTAAGTCTTAAGCC | 219333 |
rs747271974 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27077161 | AGGTGACATAAGAAA[A/G]TACTTAAGAAGTCAG | 219333 |
rs747339613 | snp | C/T | | | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162868 | CCCTCAGAGTTTGAA[C/T]GGTAACGTTTAAATG | 219333 |
rs747341850 | snp | C/T | 1.6531e-05 | 0.00287493 | intron-variant | USP12 | GRCh38.p7 | 13:27075140 | ATCTTGAATGTACCC[C/T]GCTCTTCTAACCTAG | 219333 |
rs747389878 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27083396 | TGCAAGGTGCTGTGA[A/C]GTGAAATGCAATGTT | 219333 |
rs747396295 | in-del | -/AAGT | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124011 | ATTTTGATAATATAA[-/AAGT]AACTATATATTAAAT | 219333 |
rs747406585 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27104567 | TACGTTTAGCTTTCA[C/T]TAGGGGAAACAAGAT | 219333 |
rs747434068 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129831 | CTTTGATAAATGGTG[A/G]GGAAGTAGAAAAGAA | 219333 |
rs747539901 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132017 | TTCTAGTGCTTCTAC[C/T]GGTTCTACATCTAAA | 219333 |
rs747557480 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069030 | GGCTGTTTTAAAAGA[A/G]GAGCTGGTATCTCTG | 219333 |
rs747608165 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130082 | AAACCAGCTACTATT[C/G]CCTACTCCTCAGCAT | 219333 |
rs747660523 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27097568 | GGTAGGAGGGCACAG[C/G]TGCTAGAGCAAGGCT | 219333 |
rs747716731 | snp | G/T | | | missense, utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069368 | TAGAATTCTTCAATA[G/T]CTTGTGCATCTATTT | 219333 |
rs747739732 | snp | A/G | 1.7047e-05 | 0.00291945 | synonymous-codon, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27095814 | GGCATCTTGTTGCAT[A/G]TAGTTGTCAAAAAGC | 219333 |
rs747801885 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131226 | GAGACACTTTAGCCA[C/T]AGCAGGCCAGAAGGC | 219333 |
rs747804023 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27115621 | CAACAATTATATAGC[A/G]CAAGTTTGTGATACT | 219333 |
rs747852183 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27083547 | CTCTCCTCTCACCTA[C/T]ATGCTTTAACCTCCC | 219333 |
rs747859932 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156149 | TAAAGAGACACGACA[C/T]TCCACTGCAAACCAG | 219333 |
rs747880802 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168550 | GTAGGCAGGTACTCC[A/G]TGCCAGGCCCTGAAG | 219333 |
rs747924867 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27073674 | GTGTGAGAAAGTAAA[C/T]ATTATAAAGCTAAGA | 219333 |
rs747983386 | snp | C/T | 1.65031e-05 | 0.00287251 | synonymous-codon, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105741 | ATTACCATTTTCTTT[C/T]CGTAATCTTGTGATG | 219333 |
rs747990955 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101212 | TTAGAGTATACTGAA[C/T]ATGCCAGAATTTTGC | 219333 |
rs748001927 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127309 | CTTAAAATCAGAAAT[C/T]GGCACAAAGCAAAGT | 219333 |
rs748037842 | snp | A/G/T | 6.36153e-05 | 0.00563947 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171549 | GCCGCCCGCCCGCCC[A/G/T]AGAGGTCCCGGCAGC | 219333 |
rs748063551 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27109996 | ATGATATTAAGAAAT[C/T]GTTGACTTTGTTAGG | 219333 |
rs748068889 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27109120 | TAAACAGTTGATGAA[A/G]GAAGTTTCTGTTTAT | 219333 |
rs748100446 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156916 | AACAGCATGATCCGG[C/T]GGCAAAAGCACTAGA | 219333 |
rs748120915 | in-del | -/AAAT | | | intron-variant | USP12 | GRCh38.p7 | 13:27122656 | ACCCCATCTCAAAAT[-/AAAT]AAATAAATAAATAAA | 219333 |
rs748188940 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158662 | TAAACACATCTAAAC[A/G]TAGAAAAGGTACAGT | 219333 |
rs748237326 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125957 | TGTGCTTACAGCATA[A/G]AGCAGCAGGGAAGCT | 219333 |
rs748246216 | snp | G/T | 0.000173058 | 0.00930049 | intron-variant | USP12 | GRCh38.p7 | 13:27090056 | AAATAATTATTAAAT[G/T]TCAAACTAAATAATT | 219333 |
rs748282898 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172408 | GTTTGTTTCTTTTTA[C/G]GTATATTGGATGAAT | 219333 |
rs748304249 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140639 | AAGTAACAAAACTGA[A/G]GTCTTCTCTGTAAGT | 219333 |
rs748321203 | in-del | -/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148140 | TCAAAAAAAAAAAAG[-/G]ACTTTTCTAAAACGA | 219333 |
rs748387157 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159824 | ACCTAAGTCATCATT[A/C]ACATAAAATGGCAAG | 219333 |
rs748435483 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27112878 | TTCCCAATGGATCAT[C/T]TTACACACTTCATTT | 219333 |
rs748461301 | snp | C/T | 1.77448e-05 | 0.00297861 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117750 | AGAAAAAACAAAATT[C/T]AAGAAACAAGGACCT | 219333 |
rs748479062 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27118593 | ATATGTTGAAAATAA[A/C]CAACAAACCCAGGTT | 219333 |
rs748504855 | in-del | -/TCTT | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118348 | ATATACATGATACTG[-/TCTT]TATTTTTTTGACTTG | 219333 |
rs748521039 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27093014 | CCAGCCTGACCAACA[C/T]GGAGAAACCCTGTCT | 219333 |
rs748524304 | in-del | -/GC | | | intron-variant | USP12 | GRCh38.p7 | 13:27079748 | CTATTTGCAAGCTCT[-/GC]GCCACAGATGAATGC | 219333 |
rs748539652 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27091147 | AAAGAAGAGGGAACA[C/T]AGACAACTCAGAGAG | 219333 |
rs748544269 | snp | C/T | 1.6492e-05 | 0.00287154 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069271 | AAAGTGTCTCTTCAT[C/T]ACGGTTCCCTCTCAG | 219333 |
rs748547317 | snp | C/G | 1.6631e-05 | 0.00288362 | intron-variant | USP12 | GRCh38.p7 | 13:27069435 | AGCTCTGTACAGCCA[C/G]AATGGCTTAAATTTA | 219333 |
rs748558575 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27070276 | TGATAGAAGTCCAAA[C/T]AGCAGGCTCCAGGAG | 219333 |
rs748622000 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170365 | ATGTACCACCCTTAG[A/T]TGGAAAATTTCTTGG | 219333 |
rs748679535 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27105517 | TTATCACTGTATAAC[A/G]CAATGCAAACATTAA | 219333 |
rs748793052 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27085122 | TATTCCTAAGTATTT[C/T]ATTGTTTCTAATAGT | 219333 |
rs748811928 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117466 | CAGTCTAGATGGGCC[A/G]TTGTTAGGGAAATAG | 219333 |
rs748820339 | snp | A/G | 0.000165516 | 0.00909565 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069241 | TCCAAAATAACCAGA[A/G]AAGAAATGAGGCAGA | 219333 |
rs748840895 | in-del | -/TTA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150820 | GAAAGAATAGTCTTT[-/TTA]ACAACTGGCGCTGGG | 219333 |
rs748866516 | in-del | -/C | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118322 | TTATCTTCCAGCCAA[-/C]CAGCACTTCTATATA | 219333 |
rs748885806 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27105606 | AAGAAAGGCGTGTCA[A/T]CCTTGTTTCTTCAAC | 219333 |
rs748889621 | in-del | -/TT | | | intron-variant | USP12 | GRCh38.p7 | 13:27097985 | AACTTTATATAGTAC[-/TT]TTTTTTTTTTTTTTT | 219333 |
rs748921002 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27118757 | TAAAATACCAGTCCA[C/T]ACACCTTAGGAAGGC | 219333 |
rs748922807 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165823 | AAAACTAGGGAACTA[A/T]GTGAAATTCTTGCTT | 219333 |
rs748933000 | in-del | -/AAAAT | 1.75705e-05 | 0.00296394 | intron-variant | USP12 | GRCh38.p7 | 13:27090040 | AAATATTCCAGACTA[-/AAAAT]AATTATTAAATTTCA | 219333 |
rs748987079 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27070431 | CATGTGTGTGTGACA[C/T]GGGGGGACACATGTA | 219333 |
rs749047823 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27077101 | GAATTCAAACATAAC[C/T]GAGTGTTGTACAACT | 219333 |
rs749097760 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27169975 | CTATGACCCATACAA[C/T]GTGTGTAGCTCAGCC | 219333 |
rs749106977 | snp | C/T | 3.3243e-05 | 0.00407681 | synonymous-codon | USP12 | GRCh38.p7 | 13:27095778 | AGCAATTGTATTTAG[C/T]AGGTAATTTAAGAAT | 219333 |
rs749141191 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157016 | AATTTCCTTACCTGT[A/G]AAACAGACTACTCCT | 219333 |
rs749179409 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147475 | AGGTGTCCAATTTTT[-/A]AAAAAAATACTTAAC | 219333 |
rs749180123 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27098650 | AGGCAATTTTGGTAA[A/C]AGATTTAAAATAATG | 219333 |
rs749203063 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27097714 | ACCTCACAAGGCTGG[C/G]AGGAAGATTAAAAGT | 219333 |
rs749247198 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145026 | GAGCCACGATCGCAC[C/T]ACTGCATTCCAGCCT | 219333 |
rs749261855 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27100141 | CCTTGCGTGGTTCCA[-/C]CAATTGGAAAAGTCT | 219333 |
rs749325606 | snp | G/T | 2.8939e-05 | 0.00380377 | intron-variant | USP12 | GRCh38.p7 | 13:27075428 | AAATTTCATAAAAGA[G/T]ATCCACCATGTCCTT | 219333 |
rs749344975 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161180 | TTAAGCAAATTAAAC[A/G]AACAGGGAACCTTTG | 219333 |
rs749351869 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27114049 | TCTGAAGGGAAAGCA[C/T]ATTTCTTTTTTTGTT | 219333 |
rs749371997 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160076 | TTAAAGAACGAAAAT[A/G]CCACCTTAAATACAT | 219333 |
rs749396599 | in-del | -/AAA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133627 | GCAAGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 219333 |
rs749421729 | snp | C/G | 4.89944e-05 | 0.00494922 | missense, upstream-variant-2KB, utr-variant-5-prime | USP12, USP12-AS2 | GRCh38.p7 | 13:27171601 | ACCTACCATGGTACA[C/G]ATGGAGGCGAATTTG | 219333 |
rs749424738 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27088530 | TAATAAGTGTCTCGC[-/T]GTGCCTAAATTGTTT | 219333 |
rs749458868 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27087718 | AAGAAAGAGCAAAAT[A/G]AGCCTGAACAGCTTG | 219333 |
rs749536817 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134742 | CATAATAGATAAGCC[A/T]TCTTCAATCAGTTTT | 219333 |
rs749549350 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101842 | TGAACAACTAAAATT[C/T]CCTCACTTGAGGGAG | 219333 |
rs749612222 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140831 | AATTATGTCCAAGTC[A/C]GCTGACAATGATTCT | 219333 |
rs749652016 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162208 | ATCTGATCTAATGGG[A/G]AAATTATTATTCCAT | 219333 |
rs749653926 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139614 | GAGCAAGACTCCATC[A/C]CCCAGAAATAAAAAT | 219333 |
rs749654331 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27103984 | GCCAAGAGAAATGTA[C/T]TATTAAATGAAAAGG | 219333 |
rs749692882 | snp | C/T | 8.25253e-05 | 0.00642307 | missense, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116541 | CCAAAATAGTGCTCA[C/T]TGACCGGAAACTGTT | 219333 |
rs749699305 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154652 | TTAAAGTTAAAAAAA[A/C]ACGTGGACGCATTGT | 219333 |
rs749717152 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27080392 | AAGCAAAAGGTAGGG[C/G]CTTCATCTCACAAAC | 219333 |
rs749814797 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126253 | CATACAGGCTGGTGC[A/C]CCCTGGGACAAAGCT | 219333 |
rs749818011 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164709 | ATACTGGGACTCCAA[C/T]AGAGAGTTTTCAGTT | 219333 |
rs749895917 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155973 | TTAAAAATATTTCTT[-/A]AAAAAAAACCTATAG | 219333 |
rs749903649 | snp | C/T | 1.65875e-05 | 0.00287984 | missense, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116517 | CAATGGATACTTACA[C/T]TGACTAATCCAAAAT | 219333 |
rs749903807 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126143 | GCATGGTGTTTCGAG[C/G]TCTGATAACAGACAG | 219333 |
rs749910462 | in-del | -/TC | | | intron-variant | USP12 | GRCh38.p7 | 13:27073314 | GAAAGTCAATAAACA[-/TC]TCTCTGCAATTTTCT | 219333 |
rs749923129 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135572 | CCAAAAAACTTAGCC[A/G]GGCATGGCAGCACAC | 219333 |
rs749924156 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27102475 | CCCATGGCTTTCCAA[A/G]TAAAACCCAAGCTTT | 219333 |
rs749963590 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148214 | AAGAAATACTAAAGA[A/G]AGTTGTTCAGGCTAG | 219333 |
rs749999376 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154919 | TTGAAGATGCTGCAG[C/G]GGCCAGGAGCCAAAA | 219333 |
rs750023779 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27108899 | TGAGCCAAGATGGTA[C/T]CACTGTACTCGGGCT | 219333 |
rs750123622 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27120811 | ATGAAGAAGTAATGA[A/G]ATACTCAGGCCCTTC | 219333 |
rs750197881 | in-del | -/GGCAGGC | | | intron-variant | USP12 | GRCh38.p7 | 13:27122960 | TTAGCCAGGCCTGGT[-/GGCAGGC]GCCTAGTCCCAGCTA | 219333 |
rs750208595 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27073606 | AGCAATTCTAAAAAT[C/G]TAGCATGATTTAAGT | 219333 |
rs750235074 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27103412 | AAATGCTTTTCTATT[-/A]AAAAAAATGGCTTTT | 219333 |
rs750260598 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27080160 | GGCATGCAGGCAGGG[A/G]GGCAGGAGGCATCAA | 219333 |
rs750265167 | snp | C/T | 1.65042e-05 | 0.0028726 | intron-variant | USP12 | GRCh38.p7 | 13:27069398 | TTCTGTGAGGTAAAA[C/T]GTAAACATTAGTACA | 219333 |
rs750294919 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27101111 | AATGACTTGAATGCT[C/G]TGGAAATGAGAGGCA | 219333 |
rs750409189 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27113788 | TTCTGGACTCTCCAA[C/T]AATGTAAACCTCAAG | 219333 |
rs750413408 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27112287 | TCATTTCATAGCTAC[-/T]TTTTTTTTTTTTTTT | 219333 |
rs750454417 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27081366 | ACCACATTCTTTGAT[A/C]TTCCATAAGAAGCAA | 219333 |
rs750465804 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131779 | CAAAGTATTATTCAC[A/C]ACTCCCTCTCTTAAG | 219333 |
rs750518991 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27084606 | TTTATTCTTTTTCGT[A/G]TGGATATTCAGTTTT | 219333 |
rs750565162 | snp | C/T | 1.65097e-05 | 0.00287308 | missense, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105869 | GTTGACTCTTATACG[C/T]AAGAACTTTTTCCCG | 219333 |
rs750616756 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152664 | AAAAAGAATATGTGC[C/T]GGGCGTGGTGGCTCC | 219333 |
rs750637286 | in-del | -/T | 1.682e-05 | 0.00289995 | intron-variant | USP12 | GRCh38.p7 | 13:27116498 | ATGATTCTAAAAGCG[-/T]TATCAATGGATACTT | 219333 |
rs750662440 | snp | C/T | 0.000141914 | 0.00842241 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117839 | ACCTGTGGTCCCCGA[C/T]GACCATGTGAAAGGG | 219333 |
rs750776908 | snp | A/G | 1.75708e-05 | 0.00296397 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171681 | CACAGCGGCGGCGGC[A/G]GGCGGGGGAGGAGGG | 219333 |
rs750787793 | snp | A/G | 1.66568e-05 | 0.00288585 | intron-variant | USP12 | GRCh38.p7 | 13:27090006 | ATTTTGTAGATACCA[A/G]GAAATCATGTATCTT | 219333 |
rs750878137 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27083044 | TTCACCATGTTGGTC[A/G]GGCTGGTCTCAAACT | 219333 |
rs750887186 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130797 | TTTCCTGGATGAGAA[C/T]CATTTCTGCAGGGAT | 219333 |
rs750894094 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147110 | GAATTGTAAGATGAC[C/G]AATGTCTGCTGTTTA | 219333 |
rs750934453 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27078582 | GGGAAAAGACATACC[A/G]TGTAAACACTAATCC | 219333 |
rs750964127 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144357 | AGTATTAGCCAGGCA[C/T]GGTGGTGCATACCTG | 219333 |
rs750998676 | snp | A/T | 1.67414e-05 | 0.00289317 | intron-variant | USP12 | GRCh38.p7 | 13:27090184 | AGTGAATTGTCTTTG[A/T]TTTTTTCAAATACTA | 219333 |
rs750999691 | in-del | -/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132869 | CCTTATCCTAAAGGT[-/G]AAAGCCTGGCAAACC | 219333 |
rs751079546 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27100700 | CACCCACCTCAAACA[C/G]GTCCACTAAGGCAAG | 219333 |
rs751112754 | snp | A/T | 1.92978e-05 | 0.0031062 | splice-acceptor-variant, intron-variant | USP12 | GRCh38.p7 | 13:27105946 | CAGGTATTCCCAAAC[A/T]GCAACAGAAAAAAAA | 219333 |
rs751117342 | snp | A/C | 1.65968e-05 | 0.00288065 | intron-variant | USP12 | GRCh38.p7 | 13:27089981 | CCTGTGTGAAATTCA[A/C]AACAAATTTATTTTG | 219333 |
rs751268731 | in-del | -/ATAC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136512 | CAAATAAACAAATAC[-/ATAC]ATACATACATACATA | 219333 |
rs751301910 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162040 | TTTGTCAAAGGTAAC[C/T]TGTGAGCTCCGTTAC | 219333 |
rs751400502 | snp | A/G | 0.000400909 | 0.0141525 | intron-variant | USP12 | GRCh38.p7 | 13:27116504 | TCTAAAAGCGTATCA[A/G]TGGATACTTACATTG | 219333 |
rs751405383 | snp | A/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066878 | TTACTATACCTGTAT[A/T]TTTCCCCCAACCCTG | 219333 |
rs751416921 | in-del | -/C | 2.31607e-05 | 0.00340292 | intron-variant | USP12 | GRCh38.p7 | 13:27075411 | AAATAAAAATGAAAA[-/C]AAAATTTCATAAAAG | 219333 |
rs751453912 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150978 | GATTTGGCAAAGGAT[C/T]GACACAGGATTTGGC | 219333 |
rs751472869 | in-del | -/TC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156244 | AAAAAAATCAAGGAA[-/TC]TGGTTCAGGCCTCTT | 219333 |
rs751517479 | snp | A/T | 1.64784e-05 | 0.00287035 | missense, utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069353 | TCTGATGTCAACCCG[A/T]AGAATTCTTCAATAG | 219333 |
rs751567783 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102639 | AATGATGTCTTCAAA[G/T]TTCTGATCTAACATT | 219333 |
rs751620255 | snp | C/T | 1.65745e-05 | 0.00287871 | synonymous-codon | USP12 | GRCh38.p7 | 13:27095736 | ACCATTTTGTTTTTC[C/T]TGCTTTCTCTCTTCT | 219333 |
rs751635868 | snp | C/T | 1.6773e-05 | 0.0028959 | intron-variant | USP12 | GRCh38.p7 | 13:27105701 | TTAACCTTCCTAGTA[C/T]GTCATTAATACAGTG | 219333 |
rs751654676 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27105355 | AGGCTACTGCAAGGA[C/T]CCAATGAGTTAACAC | 219333 |
rs751675311 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125804 | AGACCAGGAGACTCC[C/G]TCCCGTGCCTGGCTT | 219333 |
rs751696408 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27121546 | AGCCCCATGAAGAAA[C/T]GCAGACAGCAGAATG | 219333 |
rs751711431 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164490 | GAACAGAGAGGGCTA[C/T]ACCACCTCACACAGT | 219333 |
rs751747370 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157868 | TATCAAGTTTGTATC[-/A]GTTTACATTATTATA | 219333 |
rs751748685 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141943 | AATCATGCACTTTGG[A/G]AGGCCAAAAAAAAAT | 219333 |
rs751759545 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164980 | TCAGTAAACAGAAAA[A/C]TCTGAAAGAAAATAA | 219333 |
rs751761344 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140376 | TTTTCAATTCAGCAC[A/G]GTTATGAAAACACAC | 219333 |
rs751857721 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27098403 | CAAGAAAAAAAATTT[C/T]AAAAACTGGCAAAGG | 219333 |
rs751881952 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27092252 | ACAGTGCATGTACTT[A/T]GATAAGAAGACTCAA | 219333 |
rs751891071 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131049 | ATGACACTCAAAGTT[G/T]ATGTGTGGCATTTTC | 219333 |
rs751949958 | in-del | -/AAAAC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151781 | TGTCTTGAAAAAACA[-/AAAAC]AAAACAACAAAAAAC | 219333 |
rs751967479 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148716 | AATAATAACAGCACA[A/G]AAGAGGTAGGTTGAA | 219333 |
rs751980876 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144771 | TTTTCCCCCAGAAAT[C/T]GGGAGGAGCTGGACA | 219333 |
rs752014326 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27070146 | AGAACTACTATTACC[A/G]CAGGCAACAAGAATG | 219333 |
rs752046412 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118282 | GTTGGCAGTCAAGTT[C/T]CACCAAAACAAGACG | 219333 |
rs752056788 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27085861 | GGTACTATGGTATGT[C/T]CATACAAAAAAAATA | 219333 |
rs752090032 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132295 | GCAAAGGAGATTGGC[C/T]TATGAAGTAGAGAGG | 219333 |
rs752129044 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163895 | CTCCAGGCTTCCCAG[C/G]GGTCAAGAGGACTAC | 219333 |
rs752155941 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27099359 | GTTACACATTCCTTT[A/G]TTTTTTTAAGAGATG | 219333 |
rs752169828 | snp | C/T | 1.65217e-05 | 0.00287412 | synonymous-codon | USP12 | GRCh38.p7 | 13:27075313 | AGAGAGTTTTGTATA[C/T]CGATGAAGTTGATCC | 219333 |
rs752169848 | snp | A/G | 1.70641e-05 | 0.00292092 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171664 | GCCATCTTCCACCCA[A/G]TCACAGCGGCGGCGG | 219333 |
rs752176566 | snp | C/T | 3.28531e-05 | 0.00405284 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171577 | AGCCCCGGCCGCCCG[C/T]TCGCCGCCACCTACC | 219333 |
rs752219865 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149532 | AGTTCAGCAAGGTTG[C/T]GGGTTCTAAAATTAA | 219333 |
rs752244427 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125395 | AAAACTATGTCACAA[C/T]ACAGGATGTACTATA | 219333 |
rs752261099 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27104123 | GCAGCTTCAACCTCC[A/T]GGGCTCAAGCGATCC | 219333 |
rs752292816 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157960 | CTAGGGTCTAGCACA[C/T]AACCCAACTTAATGA | 219333 |
rs752354208 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27099826 | GTAAGTTTAGCCTGA[G/T]GGACCCATTAGCCTT | 219333 |
rs752401083 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159215 | TTCTTTAAGAGTATA[C/T]ACAGTTAAACCTGAA | 219333 |
rs752450063 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27098483 | AAGGGACTGGGAAAT[A/C]ACAATTAAAACAATG | 219333 |
rs752461973 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170578 | CATCATGTGGAAAAC[-/TG]TGGTCCTTCTGGCCA | 219333 |
rs752463777 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137065 | AATAAGTGACAAAGA[C/T]ATTGAACAAAGATAG | 219333 |
rs752490388 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27089718 | AAAATAAACATTGAG[C/T]AGAATATCATTTACC | 219333 |
rs752515881 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124246 | TCAATCTGGAATTAA[C/T]GTAATTCCTTAACTT | 219333 |
rs752525850 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27069877 | CTTGAACCCAGGAGG[-/T]TGGAGGTGGTGGTGA | 219333 |
rs752528145 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27092122 | TAGTTGGTGCTTAGC[A/G]CCCCCCAAAATGAAT | 219333 |
rs752581365 | in-del | -/G | 3.52497e-05 | 0.00419805 | intron-variant | USP12 | GRCh38.p7 | 13:27089870 | TTAAAAATCCATAAA[-/G]CTCTAAAATTACCGT | 219333 |
rs752660030 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138498 | TTAGGGCAAACACAT[C/G]AGCAGCTTGACATGC | 219333 |
rs752665721 | in-del | -/GCG | 0.00039594 | 0.0140646 | cds-indel, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171670 | TTCCACCCAATCACA[-/GCG]GCGGCGGCGGGCGGG | 219333 |
rs752693932 | in-del | -/AC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150451 | TTAAAGGAAATCTAA[-/AC]ACAGAGAAAAACATA | 219333 |
rs752766357 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141916 | AGGCTGGGCGTGGTA[A/G]CTCATGCCTGTAATC | 219333 |
rs752801607 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142244 | CATGAAGAAACAGCA[A/G]CCAAACCCAAACTGA | 219333 |
rs752814881 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166547 | AGGGCAGATAATTAA[-/C]CCTACTTTGAGACCT | 219333 |
rs752866646 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27100748 | GCTAAAGTTGAGTTG[-/A]GGGGCTGAAGAAAAG | 219333 |
rs752891990 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127979 | ACTAGAAACTCAATG[C/T]TCCTATTAGACATGT | 219333 |
rs752906173 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27095359 | TGGCCTCCTAAACTG[A/C]AAGAAAATCAAACAG | 219333 |
rs752970878 | snp | C/G | 1.658e-05 | 0.00287919 | missense | USP12 | GRCh38.p7 | 13:27095723 | CATTAGGTAAACGAC[C/G]ATTTTGTTTTTCCTG | 219333 |
rs752995654 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142863 | ACTTTGGGAGGCCGA[A/G]GCAGGCTGATCACGA | 219333 |
rs753077468 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27103606 | AACTATCAAAAAAAA[-/T]AAATAATAATAATAA | 219333 |
rs753099115 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27084234 | AATTCCTGTCTGGGT[-/G]TGGTGGCTCATGCCT | 219333 |
rs753102669 | in-del | -/TT | | | intron-variant | USP12 | GRCh38.p7 | 13:27114791 | AAAAAAAAAACAAAC[-/TT]GAGCAATATAGCAAG | 219333 |
rs753122827 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27086099 | CATTTAAGCCCAGGA[A/G]TCTGAGGCTACAGTG | 219333 |
rs753132271 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27120390 | AGGCACAGTAGCTCA[C/T]GCCTGTAATCCCAAC | 219333 |
rs753138413 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27106473 | TCATAAATATGTATT[G/T]CCTTCCTTTTCCCTT | 219333 |
rs753186835 | snp | A/C | 0.000301549 | 0.0122753 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117823 | CAACTCAATTCTGTG[A/C]ACCTGTGGTCCCCGA | 219333 |
rs753222248 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27119585 | GGCTAAAACTATTCA[A/G]AAAATTAAAAGATTA | 219333 |
rs753223857 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27072982 | GAGCAAATTATTTTC[C/T]GTTTTAAAAAGCACC | 219333 |
rs753258137 | snp | A/G | 1.7742e-05 | 0.00297837 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117797 | GCGTGTCACAGTTTC[A/G]AGAACGTGATCAACT | 219333 |
rs753267508 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154478 | TAAAAATTCTCCTTC[C/T]GTTACTTCCAAAACT | 219333 |
rs753270462 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27100057 | TCAACACTGAGACAG[A/C]CTGCAACTCAAAAAT | 219333 |
rs753325582 | in-del | -/AA | | | intron-variant | USP12 | GRCh38.p7 | 13:27084499 | GAGACAGTGAGATGA[-/AA]AAAAAAAAAAAAAAA | 219333 |
rs753377759 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147022 | GTAGAGAAGCCTGGG[G/T]CAGATCCTTCTCCAG | 219333 |
rs753411960 | snp | A/G | 3.5495e-05 | 0.00421263 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117735 | GGAATGGGGCAAAGG[A/G]GAAAAAACAAAATTC | 219333 |
rs753477049 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27119644 | ACATTCTATCGTTTC[C/T]GATCACTTTCATGAA | 219333 |
rs753549941 | snp | A/T | 8.30406e-05 | 0.00644309 | splice-acceptor-variant, intron-variant | USP12 | GRCh38.p7 | 13:27071151 | CTCGATTGGGACCAC[A/T]AAAACAAACGAAGAA | 219333 |
rs753562038 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134083 | CAGGAGTTCAAGGCT[A/G]CAGTGAGCTATGATC | 219333 |
rs753566296 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27100823 | ATAATCAGGGAGAAC[C/T]AGTAAAAAGATTTTA | 219333 |
rs753575059 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27071179 | GAAGAAGTTAATTCA[A/G]TATATTTATTAATAT | 219333 |
rs753603276 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140084 | ACATAAAAAGCTATT[C/G]ACAAAGCTCATTTCA | 219333 |
rs753603335 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124606 | TACACAAAGGAGAAC[C/T]GCCAAATCAGGCAGG | 219333 |
rs753649761 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27112427 | TAACTGGGACCTCAG[A/G]CACTCAGGCATGCAA | 219333 |
rs753724638 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154137 | TCTTCCTTAGGAAGC[A/T]CACAGCCTGAGGCCT | 219333 |
rs753771084 | snp | C/T | 1.66963e-05 | 0.00288927 | intron-variant | USP12 | GRCh38.p7 | 13:27105710 | CTAGTATGTCATTAA[C/T]ACAGTGGGAAGTAGA | 219333 |
rs753781794 | in-del | -/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165057 | AAAAGCTGGTGTGCT[-/T]TTTTTTTTTTTTAGT | 219333 |
rs753798652 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125625 | AGTGGGTACAGTCCA[A/C]GGAGGGTGAGCGGAA | 219333 |
rs753840802 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158503 | ATGTCATAGAGTGTA[C/T]TCACGCAAACCTAGA | 219333 |
rs753855643 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152758 | CCATCCTGGTTAACA[C/T]GGTGAAACCCCGTCT | 219333 |
rs753893782 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076025 | ACAGAGCAAGGCTCC[G/T]TCTCAAAAAAAAAAA | 219333 |
rs753913091 | snp | A/G | 3.51377e-05 | 0.00419137 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171687 | GGCGGCGGCGGGCGG[A/G]GGAGGAGGGGAGCCG | 219333 |
rs753928431 | in-del | -/ACACACACAC | | | intron-variant | USP12 | GRCh38.p7 | 13:27084174 | CATGTTTGCATACAC[-/ACACACACAC]ACACACACACACACA | 219333 |
rs753934915 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129584 | TTGTGGAGCACGCCT[A/G]TAGTCCCAGCTGTTC | 219333 |
rs753943751 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102739 | CCAGTCTTCTTTTTT[A/T]CGTGACAGTGACACA | 219333 |
rs753958923 | in-del | -/CT | | | intron-variant | USP12 | GRCh38.p7 | 13:27094329 | GGTAACACAGCAAGA[-/CT]CTGTCTCAAAAAAGT | 219333 |
rs754019273 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162154 | AGGGTGATGTTGATA[C/T]GTATTTATAGTACAA | 219333 |
rs754037297 | snp | A/G | 1.67265e-05 | 0.00289188 | intron-variant | USP12 | GRCh38.p7 | 13:27090015 | ATACCAGGAAATCAT[A/G]TATCTTAAAAAATAT | 219333 |
rs754070650 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27082912 | GTGATCTCGGCTCAC[C/T]GCAACCTCCGCCTCC | 219333 |
rs754101343 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155830 | AAAGGTTCAACTTAA[C/T]TTGTAAACTTTAGCC | 219333 |
rs754103474 | in-del | -/TAAGAAAT | 1.67315e-05 | 0.00289231 | intron-variant | USP12 | GRCh38.p7 | 13:27071048 | TACAACTTTCAAAAA[-/TAAGAAAT]TAAGAAACTACTTAC | 219333 |
rs754140336 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27115176 | TAAAGACAAAGCGTC[C/T]TCTGATGGTCTCTTA | 219333 |
rs754152175 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27120527 | GGGGTGGTCGTGGGC[A/G]CCTGTAATTCCAGCT | 219333 |
rs754153019 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168196 | TGTAACCGAGGGTGG[A/G]CAAGCAGCCAGGCCA | 219333 |
rs754154410 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27089417 | TTGAGACTGTTTCAA[A/G]ATAAGAAGTAACGAT | 219333 |
rs754171692 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128993 | TAATAGTAACGGAGT[C/T]CATACTCCAGATTCC | 219333 |
rs754247732 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149554 | AAAATTAATACATAG[-/C]CCATCAATTGTATTG | 219333 |
rs754256999 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27073062 | CTAAGACAGGGCTAG[C/T]AATGCACGTCTAGTA | 219333 |
rs754260464 | in-del | -/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146651 | TGAACCAATTGCTAC[-/T]CCCCTTGAAAAAGTA | 219333 |
rs754273606 | in-del | -/AATAA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149212 | TTGATTTACGGAATT[-/AATAA]AATAAAAGAGGAAAA | 219333 |
rs754300304 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27095455 | AAGAATACAGACAGA[G/T]TCCTTTTAACTGAAA | 219333 |
rs754301534 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142287 | CAAACAATTGACTTG[C/T]ACTTCTCAAAAATGT | 219333 |
rs754390149 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27108814 | ATTACAAAAATTAGC[C/T]GGGTGTGGTGGCACG | 219333 |
rs754449361 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27074292 | GTAGTCTCAGCTACT[C/G]GGGAGGCAGAGGCAG | 219333 |
rs754540321 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27074714 | TGTTGGAAAAGAAGA[C/T]GAGAAGAAGACAGAA | 219333 |
rs754549876 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156800 | GCACTCCAGCCTGGG[A/C]GACAGAGCAAGATTC | 219333 |
rs754554226 | snp | A/G | 1.65581e-05 | 0.00287728 | intron-variant | USP12 | GRCh38.p7 | 13:27069428 | ATAAATGAGCTCTGT[A/G]CAGCCAGAATGGCTT | 219333 |
rs754555069 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170416 | GTTGCATAAATAGGG[C/T]CAGTGAGGCATGAAA | 219333 |
rs754571544 | snp | C/T | | | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169554 | ATAGTACCTTTGGAA[C/T]GATCTCATTTGGCCA | 219333 |
rs754625538 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147334 | TTAGTTTGTTTCCAA[G/T]TTAGTTACGAATGTC | 219333 |
rs754642226 | snp | A/C | 1.66955e-05 | 0.0028892 | intron-variant | USP12 | GRCh38.p7 | 13:27071157 | TGGGACCACTAAAAC[A/C]AACGAAGAAGAAGTT | 219333 |
rs754650693 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27076550 | TAGGTGATTATGGTT[C/G]TTTTCTTCTAGGCCC | 219333 |
rs754669484 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135867 | AGGAAAACATGCTTT[C/T]CTTTACTTTCCAAGT | 219333 |
rs754684940 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27103994 | ATGTACTATTAAATG[A/C]AAAGGGAAATAATGT | 219333 |
rs754685499 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102670 | ACCTAATCAGGGACA[C/T]TTCCCAATGACTGAC | 219333 |
rs754748933 | in-del | -/GA | 0.000100646 | 0.00709315 | intron-variant | USP12 | GRCh38.p7 | 13:27075440 | GATATCCACCATGTC[-/GA]CTTGAATTATCAAAC | 219333 |
rs754756052 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159463 | TTACAAGTGTTCTAT[-/C]ATTAAATTTCATTTC | 219333 |
rs754761802 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155229 | TGGGACTACAGGCGC[C/G]TGCCACCATGCCCGG | 219333 |
rs754773379 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27115151 | TGATCAAATGAATCT[C/T]TCCAGGGGATAAAGA | 219333 |
rs754795694 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148993 | TTCAAGACCAGCCTG[A/G]GCAACATGGTGAGAA | 219333 |
rs754865741 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27121107 | ATGAAGCCGAGATCT[C/T]TAAAGGGTTTCTCTT | 219333 |
rs754878332 | snp | C/T | 1.66607e-05 | 0.00288619 | synonymous-codon | USP12 | GRCh38.p7 | 13:27095787 | ATTTAGTAGGTAATT[C/T]AAGAATTCATGGGCA | 219333 |
rs754887132 | in-del | -/CTGCAGTGAGCCAGGGAGGCGAAA | | | intron-variant | USP12 | GRCh38.p7 | 13:27113171 | GCCAAGAAGGTGAAG[-/CTGCAGTGAGCCAGGGAGGCGAAA]CTGCAGTGAGCCATG | 219333 |
rs754916023 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27089734 | AGAATATCATTTACC[C/T]AGTAATACTTAATGA | 219333 |
rs754966925 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27092352 | CAAGTTATTTTGTGG[A/G]TATCGACGAACTTGA | 219333 |
rs755036255 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139432 | ACCAGCCTGGGCAAC[A/G]TGGTGAAACCCCATC | 219333 |
rs755054821 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27105391 | AAAGCATTATGAAAA[C/T]AAATGCATAAGCATG | 219333 |
rs755099483 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27094809 | AACTAAATGCAATGT[-/C]CCCCCTCTAAATTGG | 219333 |
rs755111432 | snp | A/G | 1.75551e-05 | 0.00296264 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171688 | GCGGCGGCGGGCGGG[A/G]GAGGAGGGGAGCCGG | 219333 |
rs755164839 | snp | C/T | 1.74275e-05 | 0.00295186 | intron-variant | USP12 | GRCh38.p7 | 13:27090033 | TCTTAAAAAATATTC[C/T]AGACTAAAAATAATT | 219333 |
rs755182309 | snp | A/C | 3.39213e-05 | 0.00411819 | intron-variant | USP12 | GRCh38.p7 | 13:27090205 | TCAAATACTAGTAAA[A/C]CACAGTTCCCAATTA | 219333 |
rs755215272 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125883 | GAGATTGACCTGGGA[C/G]GCTGGAGCTTGGCAG | 219333 |
rs755223835 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138144 | CAACAGAAACTGTTA[C/T]ATAACATGAGTTCAC | 219333 |
rs755245252 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141973 | TACAAAAATTAGTTG[G/T]GCGTGGTACATGATG | 219333 |
rs755367641 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27083443 | GAGCCTCAGCCTCCC[C/G]CTTGCCCCCATGCCA | 219333 |
rs755420728 | snp | A/C | 1.77458e-05 | 0.00297868 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117743 | GCAAAGGAGAAAAAA[A/C]AAAATTCAAGAAACA | 219333 |
rs755430556 | in-del | -/ATAG | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150073 | ATTGTATACTTTCAA[-/ATAG]ATAGAGGAGCAGATT | 219333 |
rs755488592 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27092949 | CGCCTGTAATTCCAG[C/T]ACTTTAGGAGGCCAA | 219333 |
rs755514286 | snp | A/C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153152 | GCCTGGCCAACATGG[A/C/T]GAAACCCTGTCTCTA | 219333 |
rs755521170 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146175 | GGGAGGATAAGGTAG[A/G]TGGATCACTTAAGGT | 219333 |
rs755562626 | in-del | -/AAACACAAA | 3.48014e-05 | 0.00417127 | intron-variant | USP12 | GRCh38.p7 | 13:27089872 | AAAATCCATAAAGCT[-/AAACACAAA]CTAAAATTACCGTTT | 219333 |
rs755604377 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164017 | ACCTACATGCAGCAC[A/G]ATATAATGTAGGTCT | 219333 |
rs755639660 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27098523 | CATTTTGCCCATCAC[A/T]TTGGCAAAATAAAAA | 219333 |
rs755654545 | in-del | -/TT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165056 | AAAAAGCTGGTGTGC[-/TT]TTTTTTTTTTTTAGT | 219333 |
rs755679282 | snp | C/T | 3.31203e-05 | 0.00406928 | synonymous-codon, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116522 | GATACTTACATTGAC[C/T]AATCCAAAATAGTGC | 219333 |
rs755681462 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145006 | CAGGATGTCGAGGCT[A/G]CAGTGAGCCACGATC | 219333 |
rs755714636 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132657 | CTGTCCTAAAAGATC[A/G]TTGGTTTCAAGTTCT | 219333 |
rs755723332 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27106998 | CTAATGAGATATAGT[C/G]TAATCATTTTAAAAA | 219333 |
rs755736352 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152418 | ACCAAAGTCCAAAGC[A/T]GATAATTATATAAAC | 219333 |
rs755768901 | snp | G/T | 1.77521e-05 | 0.00297921 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117728 | GGAATTGGGAATGGG[G/T]CAAAGGAGAAAAAAC | 219333 |
rs755786373 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131028 | TATAGAAATAACAAG[A/T]GCTGAATGACACTCA | 219333 |
rs755834118 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27084948 | GAATTTTGATAGGGA[A/C]TGCACTGAATCTCTA | 219333 |
rs755841767 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27090980 | TATAGACAGTTGAAG[A/G]GAGTTCCAATGGTGA | 219333 |
rs755924806 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152520 | AGCTAAAGGGTATAA[A/T]GTATCGTTCAAGATG | 219333 |
rs755989167 | in-del | -/TTAATGAA | | | intron-variant | USP12 | GRCh38.p7 | 13:27102010 | TGTATTTCCCATTTT[-/TTAATGAA]TGAATGAATGAATGA | 219333 |
rs756002834 | snp | A/G | | | synonymous-codon | USP12 | GRCh38.p7 | 13:27090150 | AAAATCTTCATCTTT[A/G]CTGCTTATCTGTAAA | 219333 |
rs756029424 | snp | C/G | 1.65729e-05 | 0.00287857 | missense | USP12 | GRCh38.p7 | 13:27095738 | CATTTTGTTTTTCCT[C/G]CTTTCTCTCTTCTTG | 219333 |
rs756036048 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27076853 | AGTGAATGAACTTGG[A/C]CTTTTGGAAACATTA | 219333 |
rs756036629 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27104284 | AGTCCACCTACCTTG[G/T]CCTCCCAAAGTGCTG | 219333 |
rs756060507 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124298 | ATCTACATCTAAAAC[C/G]AGATTATGGCTAAAA | 219333 |
rs756094966 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158011 | CAATGGACCTGATTG[C/T]GCCATTAGTTTTACT | 219333 |
rs756105281 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27104291 | CTACCTTGGCCTCCC[A/G]AAGTGCTGGGATTAT | 219333 |
rs756109028 | in-del | -/GCG | 0.00039594 | 0.0140646 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171669 | TTCCACCCAATCACA[-/GCG]GCGGCGGCGGCGGGC | 219333 |
rs756109483 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170921 | AGAGAATTTCAACAG[C/T]ACTTATTTAAAGTTT | 219333 |
rs756164324 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27169812 | AAGAAAACAGGGGCT[G/T]CCCTGACCAATACTG | 219333 |
rs756193859 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27095422 | CAGGTATTCATTGTC[A/C]ATAAGCAACATTACA | 219333 |
rs756195144 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127989 | CAATGTTCCTATTAG[A/T]CATGTCAAAAAGCAC | 219333 |
rs756204195 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166689 | TGGTATTTAAAACTA[C/G]AGTTTTCAAGCATAT | 219333 |
rs756269699 | snp | C/T | 2.48858e-05 | 0.00352736 | intron-variant | USP12 | GRCh38.p7 | 13:27075416 | AAAATGAAAACAAAA[C/T]TTCATAAAAGATATC | 219333 |
rs756284910 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142250 | GAAACAGCAGCCAAA[A/C]CCAAACTGAGGAACG | 219333 |
rs756303094 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161038 | AAACCTTCTAAACAT[C/T]ATATCCCGTTTTGTG | 219333 |
rs756322951 | snp | C/G | 5.14615e-05 | 0.00507229 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | USP12, USP12-AS2 | GRCh38.p7 | 13:27171595 | GCCGCCACCTACCAT[C/G]GTACAGATGGAGGCG | 219333 |
rs756328174 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27074129 | TCAGAGGCCGGGCGC[A/G]GTGGCTCACGCGTGT | 219333 |
rs756346475 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066902 | AACCCTGACCCTATA[C/T]GTTTTAAAAGTACAT | 219333 |
rs756348805 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27113895 | TTGCCTAATGAACTT[C/T]ATAACCCAAAAATGG | 219333 |
rs756388060 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27081507 | CCTCCACTGAAGTTC[A/G]AATCCCTCAAAGTCA | 219333 |
rs756427566 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27119616 | TGTGATTTCTAAAAT[A/C]CCTTCTCACTCAACA | 219333 |
rs756517536 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27118655 | ACTGGCTTATTCAAA[C/T]GAGTATAATCCTTTC | 219333 |
rs756549123 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133972 | TCCCATCTCTAAATA[A/G]ATAAAATAAAAACAT | 219333 |
rs756567935 | snp | A/G | 1.6674e-05 | 0.00288734 | intron-variant | USP12 | GRCh38.p7 | 13:27090010 | TGTAGATACCAGGAA[A/G]TCATGTATCTTAAAA | 219333 |
rs756600788 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27073053 | CATAAAGCACTAAGA[C/G]AGGGCTAGCAATGCA | 219333 |
rs756610649 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164631 | CTGCCACTCTAACCT[C/T]CTAAAGCAAATTCTG | 219333 |
rs756657191 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140788 | ATTGCAAAATATTCA[C/T]TTGCTCTAACAAGAG | 219333 |
rs756698773 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27101091 | ATATTCACAAAAATA[A/C]CTCCAATGACTTGAA | 219333 |
rs756763416 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134130 | GCCTGGGTCACAGAG[A/C]CAGACCCTGTGAAAA | 219333 |
rs756764994 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27086600 | ATGTCTTTAAAACAA[A/T]GAGCTCGATTTTACA | 219333 |
rs756820251 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134376 | ATTCTGAAAAGAGAC[A/T]CAGAAAAAAAGAGGA | 219333 |
rs756851405 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147055 | CCTTCAGAGAGGGCA[C/T]GGTCCTGGTGAGATG | 219333 |
rs756908452 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27073113 | CAGCACCACATGGAG[A/C]CTGAGGCTGGGCAGA | 219333 |
rs756936444 | snp | C/T | 0.00025951 | 0.011388 | intron-variant | USP12 | GRCh38.p7 | 13:27105948 | GGTATTCCCAAACTG[C/T]AACAGAAAAAAAAAA | 219333 |
rs757054470 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140241 | AGTGACTGGAGGGAG[C/T]GAAACAGTGGTTTCA | 219333 |
rs757091747 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27095194 | GATTTTTTCCCCTCC[-/T]TGAGGGTACACTGTA | 219333 |
rs757148942 | in-del | -/CA | | | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168994 | CTCTCCACCATTCCA[-/CA]CACACACACAGCCAC | 219333 |
rs757152447 | in-del | -/CCTGTTGG | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172556 | AGGAGAGGAGCGAAA[-/CCTGTTGG]CCTGTTGGCCTGTTG | 219333 |
rs757199255 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158585 | GGCCACAAACCTGTA[C/T]AGCATATGACTGTAC | 219333 |
rs757268174 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173702 | CAAAAATTAGCCAGG[C/T]GTAGCAGTGTACGCC | 219333 |
rs757272234 | in-del | -/CTCGT | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170895 | TCGTGCCTCTCAGAG[-/CTCGT]GAGAAAATGGAGAGA | 219333 |
rs757279905 | in-del | -/GA | | | intron-variant | USP12 | GRCh38.p7 | 13:27072507 | TAAACACACTCAGTT[-/GA]GTAGATACAAATGCG | 219333 |
rs757285382 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161272 | CAAAGTTATAACGGC[C/T]AGATTTTTGGACTAA | 219333 |
rs757291878 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27082913 | TGATCTCGGCTCACC[A/G]CAACCTCCGCCTCCC | 219333 |
rs757333355 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129599 | GTAGTCCCAGCTGTT[C/T]GGGAGGCTGAGGCAG | 219333 |
rs757348603 | snp | C/T | 0.000100565 | 0.0070903 | intron-variant | USP12 | GRCh38.p7 | 13:27105703 | AACCTTCCTAGTATG[C/T]CATTAATACAGTGGG | 219333 |
rs757367653 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27115244 | AGAATTCTAACTGAA[A/G]TGCTGTTTTTTAAAT | 219333 |
rs757385200 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27081784 | TTATGTTAGCAGGCA[A/T]GAAAACAACATTAAT | 219333 |
rs757419177 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156621 | TCAGAAGTTTGAGAC[C/T]AGCCTGGCCAACATG | 219333 |
rs757497921 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27087775 | AATGACTGGGCACAT[A/C]AAGAAGAGAGGAGCC | 219333 |
rs757511048 | in-del | -/AT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132359 | AAATTTTAGTTACAC[-/AT]GTTAAAAAATGTATA | 219333 |
rs757511612 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102765 | ACACATTACATCACA[C/T]AATTGATGGCTGTCT | 219333 |
rs757555115 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162269 | CCAAGTGAAAATAAT[C/T]AGTGAGGACTCAAAG | 219333 |
rs757561552 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156547 | GAGGCTGGGGGGGCA[A/G]TGGCTCACGCCTGTA | 219333 |
rs757564052 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116540 | TCCAAAATAGTGCTC[A/G]TTGACCGGAAACTGT | 219333 |
rs757566146 | in-del | -/CA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152941 | AGCGAGACTCCGTCT[-/CA]AAAAAAAAAAAAAAA | 219333 |
rs757597613 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27106821 | TGAAAGAATGTTGTT[A/G]TAAAACATTTACTTT | 219333 |
rs757623249 | in-del | -/GAA | 6.71237e-05 | 0.00579287 | intron-variant | USP12 | GRCh38.p7 | 13:27071161 | ACCACTAAAACAAAC[-/GAA]GAAGAAGTTAATTCA | 219333 |
rs757652349 | in-del | -/A/AA/AAA | | | intron-variant | USP12 | GRCh38.p7 | 13:27088416 | GCGAGACTCCGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 219333 |
rs757703510 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142986 | TAGTCCCAGCTACTT[C/G]GGAGGCTGAGGCAGG | 219333 |
rs757714344 | in-del | -/GG | | | intron-variant | USP12 | GRCh38.p7 | 13:27076099 | AATTCCTTTGGACTT[-/GG]GTAGACTGAAATCTA | 219333 |
rs757761974 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27095462 | CAGACAGATTCCTTT[C/T]AACTGAAAAATACAT | 219333 |
rs757762525 | snp | A/G | 5.91069e-05 | 0.00543599 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171583 | GGCCGCCCGCTCGCC[A/G]CCACCTACCATGGTA | 219333 |
rs757762594 | snp | G/T | 1.65321e-05 | 0.00287502 | intron-variant | USP12 | GRCh38.p7 | 13:27075141 | TCTTGAATGTACCCT[G/T]CTCTTCTAACCTAGG | 219333 |
rs757810388 | in-del | -/TTTCTTTC | | | intron-variant | USP12 | GRCh38.p7 | 13:27085161 | TGGAATGTTTTCTTT[-/TTTCTTTC]TTTCTTTCTTTCTTT | 219333 |
rs757830132 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128078 | GCTAAATGTGTTATA[C/G]AGAATATTTAGAGAG | 219333 |
rs757850604 | snp | A/G | 4.98153e-05 | 0.00499051 | synonymous-codon | USP12 | GRCh38.p7 | 13:27075348 | ATTTAAATCTCTTCA[A/G]GTGTAGAGCTAGAAT | 219333 |
rs757884771 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27089595 | TCACCAAGAAAAAAG[C/T]TTACATCATCAGGAA | 219333 |
rs757942395 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27120933 | GTGATGGGGGAACTA[C/T]GAGAGATAAGCAAAC | 219333 |
rs757951193 | in-del | -/TTCTT | | | intron-variant | USP12 | GRCh38.p7 | 13:27085178 | TCTTTCTTTCTTTCT[-/TTCTT]TTTTTTTTGAGATGG | 219333 |
rs757961837 | snp | C/G | 1.65072e-05 | 0.00287286 | synonymous-codon | USP12 | GRCh38.p7 | 13:27075301 | AACTACCCGGTAAGA[C/G]AGTTTTGTATATCGA | 219333 |
rs757970563 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27102502 | CTTTAGGCCCCTGTT[A/C]TTCTGACTTTATCTT | 219333 |
rs757996503 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27088026 | AAGTGAAGAACTCTG[C/T]AAAACATCTGGGGAA | 219333 |
rs758015543 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156627 | GTTTGAGACCAGCCT[A/G]GCCAACATGGTGAAA | 219333 |
rs758020505 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27074408 | CCATCTCAAAAAGAA[A/C]AAAAAAAAATTCTAA | 219333 |
rs758062143 | in-del | -/AA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131588 | CCACTATGTAAATGG[-/AA]AAGAGACCACTCTTT | 219333 |
rs758103953 | snp | C/T | 1.6501e-05 | 0.00287232 | missense, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105742 | TTACCATTTTCTTTC[C/T]GTAATCTTGTGATGA | 219333 |
rs758107235 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156015 | ACTGTATTCTGAAGC[C/T]CTAATGAAACACTGG | 219333 |
rs758138446 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27122082 | TGCCTGTAATCCCAG[C/G]ACTTTGGGGAGGCTA | 219333 |
rs758150174 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27113805 | ATGTAAACCTCAAGT[A/G]ACCTATGGCCATCAG | 219333 |
rs758229915 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27112843 | AAATAAACATCAGAA[A/G]TGCTAATATTTTCTT | 219333 |
rs758237040 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154982 | GAAACAGTCCCTCCT[A/G]CAGCTCCAGGAAAGA | 219333 |
rs758254254 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27109641 | AGTCATCTTTGGCTG[C/G]GCGCAGTGGCTCAAG | 219333 |
rs758346746 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101182 | ATTTCTAAGATTATT[C/T]GTAGTCCATTTTCCT | 219333 |
rs758446714 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152668 | AGAATATGTGCCGGG[A/C]GTGGTGGCTCCCGCT | 219333 |
rs758448388 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27119045 | CTACTTTATAGGGTG[A/G]CTATAACAGAATTTT | 219333 |
rs758502964 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27104554 | CTAATAAAGTACATA[C/T]GTTTAGCTTTCATTA | 219333 |
rs758535192 | snp | C/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069001 | AAAGAGAAAATGCGT[C/G]CCAATGACTGGAAGG | 219333 |
rs758535299 | snp | A/G | 3.16992e-05 | 0.00398103 | intron-variant | USP12 | GRCh38.p7 | 13:27095580 | AATTTTTCTCTATAC[A/G]AAATTGTATGATATA | 219333 |
rs758572545 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27092601 | TGACAAAGGAGCAAA[A/G]GCAATTCAACAGAGA | 219333 |
rs758583449 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163515 | AATTACCATTACTTA[C/T]ACCAATAAGAAAAAC | 219333 |
rs758632152 | snp | C/T | 4.9717e-05 | 0.00498558 | synonymous-codon | USP12 | GRCh38.p7 | 13:27095727 | AGGTAAACGACCATT[C/T]TGTTTTTCCTGCTTT | 219333 |
rs758646640 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101143 | AGTAAACCAAAAAAA[-/T]AATCTTTAAACTTTT | 219333 |
rs758695678 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144393 | TTAGCTACTCAAGAG[A/G]CTGAGGCAGGATGTT | 219333 |
rs758725294 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129700 | TCTTAATAATAATAA[C/T]AGCAAATAAAAATAA | 219333 |
rs758727872 | in-del | -/AAA | | | intron-variant | USP12 | GRCh38.p7 | 13:27084498 | AGAGACAGTGAGATG[-/AAA]AAAAAAAAAAAAAAA | 219333 |
rs758743361 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27097302 | GAAAGTCCGTCTCTA[C/T]TAAATACAAAAAATT | 219333 |
rs758744601 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27078761 | TAGAAATAGACAAGT[G/T]CATAATCAGAATTGG | 219333 |
rs758779069 | snp | A/G | 1.81833e-05 | 0.00301518 | intron-variant | USP12 | GRCh38.p7 | 13:27071174 | ACGAAGAAGAAGTTA[A/G]TTCAATATATTTATT | 219333 |
rs758829355 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076307 | GTTTTTAACTGTGAA[A/T]CACAGGCTGTTCTTC | 219333 |
rs758926744 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124005 | CCTATTATTTTGATA[A/G]TATAAAAGTAACTAT | 219333 |
rs758930884 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27116348 | AGATGTCAGGCAACT[C/T]TGTTTCCCTTCCCTT | 219333 |
rs758947417 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27114925 | AGGAGGTGAAGGCTG[-/C]AGTGAGCTGTGATGG | 219333 |
rs758974841 | snp | A/T | 8.86973e-05 | 0.00665889 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117832 | TCTGTGCACCTGTGG[A/T]CCCCGACGACCATGT | 219333 |
rs758974996 | in-del | -/AA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157546 | TTTTAAAAAAAATAT[-/AA]GTTTATAGAAGATTT | 219333 |
rs758984997 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27086317 | CACACACAATGCAGC[A/C]CCTCCTAAGAAGGAT | 219333 |
rs759005839 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147213 | GCCTACACCCTCAGA[A/G]CCACTGCCTTTTTAA | 219333 |
rs759013431 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138400 | GATGGTAAATTTATG[A/G]ACAGAAGCAATGTCT | 219333 |
rs759014313 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27091952 | TGGGTTAGGTCTACT[A/G]TTCTCTGGCTGGCAT | 219333 |
rs759043409 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139703 | CATGCAAGTCCCACC[C/G]TAAATTCTTTCATGT | 219333 |
rs759096088 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153516 | GACAAGAGTGGAAAC[A/G]TCACTTCCATAACAA | 219333 |
rs759127921 | snp | C/G | 0.000171006 | 0.0092452 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171566 | GAGGTCCCGGCAGCC[C/G]CGGCCGCCCGCTCGC | 219333 |
rs759130737 | in-del | -/ACACACACACACAC | | | intron-variant | USP12 | GRCh38.p7 | 13:27084170 | AATCCATGTTTGCAT[-/ACACACACACACAC]ACACACACACACACA | 219333 |
rs759184592 | snp | C/T | 7.54594e-05 | 0.00614199 | missense, upstream-variant-2KB, utr-variant-5-prime | USP12, USP12-AS2 | GRCh38.p7 | 13:27171636 | CTGTCATTAGGATTT[C/T]CATCCGGCCAGCGCC | 219333 |
rs759192323 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158418 | TAAATTTCTGTTACA[A/G]GCATGCACCACTTAA | 219333 |
rs759204727 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27093420 | AGATGATAAATAAGC[A/G]GACAAAAAGATGATC | 219333 |
rs759227278 | in-del | -/GGGA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144110 | TCGGGAGGCTGAGGT[-/GGGA]GGATCACTTCAGCCT | 219333 |
rs759238043 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125318 | AGCTTTTCATGATTA[C/T]ATATAAATAAAAATC | 219333 |
rs759303834 | in-del | -/ACAG | 0.000301587 | 0.0122761 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117769 | AAACAAGGACCTCGC[-/ACAG]ACAATCATAGCGTGT | 219333 |
rs759315302 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170740 | GTCCCCGCACAGACA[A/G]ACCTAGCTCCAGCCA | 219333 |
rs759330334 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27116128 | CCATCCTGGCTAACA[C/T]GGTGAAACCCTGTCT | 219333 |
rs759360176 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131511 | TACCAAAGTGAGCAA[C/T]GTGATGGAAACTTGC | 219333 |
rs759392087 | snp | C/T | 0.00028404 | 0.0119138 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117712 | AAGAGGGATGGACCA[C/T]GGAATTGGGAATGGG | 219333 |
rs759398642 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27091731 | CCGACAATGAAACCC[C/T]GGGGAACACCCACAT | 219333 |
rs759422176 | snp | A/G | 3.37735e-05 | 0.00410921 | missense | USP12 | GRCh38.p7 | 13:27089884 | AGCTCTAAAATTACC[A/G]TTTGTGTGCTTCCTG | 219333 |
rs759440182 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130290 | GTTTTTTTCCCTTTA[C/T]TGAGGGGGATGGGGA | 219333 |
rs759441927 | in-del | -/TA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142479 | AAATTATACCATCTT[-/TA]TATGAAAGAGAATGT | 219333 |
rs759473617 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168022 | AGACAGCCAGTTTCA[C/G]CTGTGCCTTTCTTCA | 219333 |
rs759501205 | snp | C/G | | | missense, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105875 | TCTTATACGCAAGAA[C/G]TTTTTCCCGAAATGG | 219333 |
rs759526178 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27104000 | TATTAAATGAAAAGG[C/G]AAATAATGTATGCTC | 219333 |
rs759529043 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27089154 | TAATGTGGGATTCTG[C/G]ACAGAATCCTTCTTC | 219333 |
rs759620028 | in-del | -/TGTGTGTGTGTGTG | | | intron-variant | USP12 | GRCh38.p7 | 13:27087254 | TAGTGGGGAGGGATG[-/TGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 219333 |
rs759648218 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135056 | TTGGGAGGACGAGGT[G/T]GGCAAATCCCTTGAG | 219333 |
rs759727888 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166337 | ATACAAATGCTTAAA[A/C]GATACTTCCTGAGAC | 219333 |
rs759738089 | in-del | -/AAAG | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117109 | AAAAGAAAAAGGAGA[-/AAAG]AAAGAATGATATTGA | 219333 |
rs759749144 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146806 | TTCAGTACTTCATAA[C/T]GTAACCTTATTTAGA | 219333 |
rs759837738 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159029 | ATCCCAACTCTTTCT[A/G]GCAATTACTTCTTGG | 219333 |
rs759876954 | snp | C/T | 2.24792e-05 | 0.00335248 | intron-variant | USP12 | GRCh38.p7 | 13:27095852 | ATAAAAACATTATAT[C/T]AGAGAATTATTTCAG | 219333 |
rs759880744 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126686 | CAGCAAGACAGGAGA[C/T]CAGATTTGTAGCACC | 219333 |
rs759939868 | in-del | -/GAG | 3.31186e-05 | 0.00406918 | cds-indel | USP12 | GRCh38.p7 | 13:27069239 | TTTCCAAAATAACCA[-/GAG]AAGAAATGAGGCAGA | 219333 |
rs759961706 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27113215 | GTGAGCCATGATCAC[C/T]CACTGCACTCCAGCC | 219333 |
rs759982844 | in-del | -/TCT | | | intron-variant | USP12 | GRCh38.p7 | 13:27102728 | TGTCCCCTTTCCCAG[-/TCT]TCTTTTTTTCGTGAC | 219333 |
rs760000012 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173268 | TTCTACCCCCTGTTT[C/G]GACAAGGGTTTCTAC | 219333 |
rs760071977 | in-del | -/AAA | | | intron-variant | USP12 | GRCh38.p7 | 13:27103599 | AACTATTGAACTATC[-/AAA]AAAAAAAATAATAAT | 219333 |
rs760146366 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125494 | AGAGTTGCTTCCAAG[A/G]TGGCCGAATAGGAAC | 219333 |
rs760177137 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27083796 | ATACTAATTTTGTGG[C/T]ACATCATTAACATTC | 219333 |
rs760194033 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27073191 | GCAATGAGAGTGAGA[A/C]AGGAGAAAGAGTAAG | 219333 |
rs760203022 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159505 | ACACCTATTCAATCC[A/G]GCCTTCTCTATCAAT | 219333 |
rs760222391 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141406 | TAGTAATGAGCACAC[A/G]TAGAATCGGCATCTT | 219333 |
rs760226837 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27095047 | GTGGTCCTTGCTACT[C/T]ATGAGGCTTAGATGG | 219333 |
rs760353098 | in-del | -/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149317 | TGGATGCTTTTCCTC[-/T]TAAGATTAGGAAAAA | 219333 |
rs760376331 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27113529 | CAGCAGAGTAGACCA[C/G]ACATTGAGTACCTCA | 219333 |
rs760399068 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160589 | TTTGTTTTTGGTCCG[C/T]TGTATCTAGTTTTTG | 219333 |
rs760439156 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27094417 | GAGGCAGGAGGATCA[A/C]TTGAGCCCAGGAGTC | 219333 |
rs760453687 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154017 | AAATTAGAGCTTCTT[C/G]TGATACTATCTTTAA | 219333 |
rs760454717 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27121236 | AGGAGAAACATCTTC[C/T]CAAAATTCATAACCA | 219333 |
rs760471173 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27093815 | TAAAAACTGCAGCAC[A/G]TCCTTACAGTGGAAA | 219333 |
rs760502670 | snp | C/T | 1.65375e-05 | 0.0028755 | missense, intron-variant | USP12 | GRCh38.p7 | 13:27071138 | GCAATATAATGGCCT[C/T]GATTGGGACCACTAA | 219333 |
rs760519108 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27071370 | GTACTCTAAGAGATA[C/T]ATCAGTATTCTTTTC | 219333 |
rs760521628 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27105225 | ATTAAAACTTATCTA[C/T]CCTAAGCCAAAAGGT | 219333 |
rs760603907 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157201 | TAATGTGGTAATCAT[A/G]TTTTGTTGGTTTTTT | 219333 |
rs760639934 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164022 | CATGCAGCACGATAT[A/C]ATGTAGGTCTCCATG | 219333 |
rs760688929 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27092133 | TAGCACCCCCCAAAA[C/T]GAATACTTAAATATA | 219333 |
rs760739859 | snp | C/T | 1.64803e-05 | 0.00287052 | missense, utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069290 | GTTCCCTCTCAGTCC[C/T]GAGACTGATAGAAAA | 219333 |
rs760741199 | in-del | -/TCTACTGCACCCCCAAGGAATTCAAAGCATTATTGGTG | 1.64808e-05 | 0.00287057 | frameshift-variant, utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069362 | ACCCGTAGAATTCTT[lengthTooLong]CAATAGCTTGTGCAT | 219333 |
rs760766961 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142906 | GAGACCATCCTGGCC[A/G]ACATGGTGAAACCCC | 219333 |
rs760784132 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102232 | GTCAACTCTAGCTAA[C/T]ACAATCAGATCACCA | 219333 |
rs760807193 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27108743 | AGGTGGATCAGTTGC[A/G]GTCAGGAGTTTAAGA | 219333 |
rs760815993 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27075922 | ATAGTCCCAGCTACT[C/T]GGGAAGCTGGGGCAG | 219333 |
rs760825239 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27097813 | ACTACATGTTGAATA[C/T]CCTTTATCTAAAATG | 219333 |
rs760868461 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146497 | AGGATAGAATCAAGC[A/C]ATTAGTTAACTACAC | 219333 |
rs760881635 | snp | A/C/G/T | 5.04588e-05 | 0.0050227 | intron-variant | USP12 | GRCh38.p7 | 13:27116498 | CATGATTCTAAAAGC[A/C/G/T]TATCAATGGATACTT | 219333 |
rs760884001 | in-del | -/CA | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068923 | TCCTTATCAATACGG[-/CA]CAGATTCCGATTCTT | 219333 |
rs760905467 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135300 | CATAAAATGAAAACA[C/T]TTAGAATTTATTTTG | 219333 |
rs760915196 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27110500 | TACCAACTTTTTGAA[G/T]AGGCTTGTGAGATCC | 219333 |
rs760915964 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102358 | CTCCAGGCTGGTCTC[C/T]TGCCTCTACTCTCAT | 219333 |
rs760991505 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167522 | GTAATAGAAGATTCC[G/T]TATTTTTGAGGTTTT | 219333 |
rs760994855 | in-del | -/TGTGTGTGTG | | | intron-variant | USP12 | GRCh38.p7 | 13:27087258 | GGGGAGGGATGTGTG[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 219333 |
rs761001984 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27114528 | ATATCAGGAATAGCA[C/T]TGTATCTACAGGAGA | 219333 |
rs761082428 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150250 | TAATAAAGCAAAAAA[C/T]TGTATTTATATATGC | 219333 |
rs761104217 | snp | C/T | 1.67618e-05 | 0.00289493 | intron-variant | USP12 | GRCh38.p7 | 13:27090190 | TTGTCTTTGATTTTT[C/T]CAAATACTAGTAAAC | 219333 |
rs761147423 | in-del | -/C | 6.73185e-05 | 0.00580127 | intron-variant | USP12 | GRCh38.p7 | 13:27105694 | ACTATATTTAACCTT[-/C]CTAGTATGTCATTAA | 219333 |
rs761155032 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27100784 | AACCAACTGGAAAAG[G/T]CCTAGAGGAATCTAA | 219333 |
rs761158853 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27086541 | TCTAATTTAATTACA[A/G]AGAATATACATTCTT | 219333 |
rs761179590 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27119698 | TAACACAAAACTCCA[-/G]GGAAGTCTAAGACAA | 219333 |
rs761189133 | in-del | -/ACACACACACAC | | | intron-variant | USP12 | GRCh38.p7 | 13:27084172 | TCCATGTTTGCATAC[-/ACACACACACAC]ACACACACACACACA | 219333 |
rs761194723 | snp | C/G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27074138 | GGGCGCGGTGGCTCA[C/G/T]GCGTGTAATCCCAGC | 219333 |
rs761208302 | snp | C/T | 1.66045e-05 | 0.00288132 | missense | USP12 | GRCh38.p7 | 13:27095702 | TATTTTCATTATCAA[C/T]ATTACCATTAGGTAA | 219333 |
rs761227233 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066533 | TGATGGTTAGAGGCC[C/T]CAAGACCCACATAAT | 219333 |
rs761261097 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136565 | TGAAATTCTTCTTCA[A/G]TGGAGAGAATAGATA | 219333 |
rs761341858 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148146 | AAAAAAAAAGACTTT[C/T]CTAAAACGAAAACCT | 219333 |
rs761381137 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128729 | GGATTGCCACCCTGC[A/G]TACCCTTCAGACACC | 219333 |
rs761395018 | snp | A/G | 1.67047e-05 | 0.00288999 | missense | USP12 | GRCh38.p7 | 13:27095669 | CATGAACCCACGTTG[A/G]GTCTGGTGTGCTGTT | 219333 |
rs761440023 | in-del | -/AAAAC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144693 | TGACTGTGGTTCAAA[-/AAAAC]AAAACAGAAAGACCA | 219333 |
rs761517954 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27088644 | ACATGACTAGCCCCA[A/G]ATAAAAACTCAGGGC | 219333 |
rs761557558 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27102413 | AAAGGGTCTTCTCAA[A/G]CAAATCAGAACGTAT | 219333 |
rs761574329 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27082945 | GGTTCAAGTGATGCT[-/C]CTGCCTCAGCCTCCC | 219333 |
rs761574557 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27097433 | TTGCGCCATTGCACT[A/C]CAGCCTGGGCAACAA | 219333 |
rs761578018 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067980 | ACACAGATTTTAATT[C/T]CTGAACACCCTTCCA | 219333 |
rs761617486 | snp | C/T | 4.95405e-05 | 0.00497673 | missense, intron-variant | USP12 | GRCh38.p7 | 13:27071118 | AATCATGACTCTTAA[C/T]TATTGCAATATAATG | 219333 |
rs761653817 | snp | C/T | 3.29647e-05 | 0.00405971 | missense, utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069369 | AGAATTCTTCAATAG[C/T]TTGTGCATCTATTTT | 219333 |
rs761670596 | snp | A/C/T | 3.54832e-05 | 0.00421195 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117783 | CACAGACAATCATAG[A/C/T]GTGTCACAGTTTCAA | 219333 |
rs761670769 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142619 | TATTTGGGAACTTCT[G/T]GCATTATTCTTGCAA | 219333 |
rs761681119 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27093942 | AAACAGGCTGCATAC[C/T]ATATGATTTCAACTA | 219333 |
rs761755164 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127363 | CCAATGACATAAAAG[A/G]GAACAGAGAGGTTCA | 219333 |
rs761758706 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145285 | ATGGCAATGGTAGCT[C/G]CTAAGAATCAACTTT | 219333 |
rs761849320 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27098122 | AAGTAAAGTTGTTAC[G/T]ACCTCAGCCACCCCA | 219333 |
rs761851598 | in-del | -/AAAG | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067773 | TGAAAAGAGTTTAAT[-/AAAG]AACATCCAAGGCCTG | 219333 |
rs761873634 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27095126 | GGCCACTGCACTCCA[A/G]CCTGGGTGTAACAAT | 219333 |
rs761890135 | in-del | -/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068013 | AAGATTTGTAAAGGT[-/G]GGGGGAAGGGAAGGA | 219333 |
rs761901746 | snp | A/G | 6.8899e-05 | 0.00586896 | intron-variant | USP12 | GRCh38.p7 | 13:27116480 | TTTAAAACTGCTTCC[A/G]AACATGATTCTAAAA | 219333 |
rs761909537 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163415 | ATAATAAAGGCCATT[C/T]ATTTTGCAAAGTTCA | 219333 |
rs761958675 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131615 | TCTTTAACCTATGTA[A/G]AAGTCTGAGGTTAGC | 219333 |
rs762011221 | snp | A/C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27110655 | AAAGCGTACTGATAT[A/C/T]AATGATCATAAATGT | 219333 |
rs762036561 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27121930 | TCATATGTGTCAAGA[A/C]ATGGCAATGAATTGA | 219333 |
rs762102296 | in-del | -/A | 0.0240487 | 0.106986 | intron-variant | USP12 | GRCh38.p7 | 13:27105954 | CCCAAACTGCAACAG[-/A]AAAAAAAAAGTTTTG | 219333 |
rs762117411 | in-del | -/ACAAA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136169 | CAAAACTTCAAGGCT[-/ACAAA]CCTAAGTCCAAGTCT | 219333 |
rs762144666 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27103202 | CAGTGAAAGTCAGTG[G/T]AAATACTGAAATGAG | 219333 |
rs762161143 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102675 | ATCAGGGACATTTCC[C/T]AATGACTGACATATG | 219333 |
rs762195621 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168287 | TCCCCCTCCCAACAA[C/T]GCCTTCCTAACCATG | 219333 |
rs762230373 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157494 | AATGAGTTCTGTAAG[A/C]TACAAATGTGATTTT | 219333 |
rs762230434 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27109537 | TGACTTGAAAAAAGG[C/T]TGAAAAGGACTCAAG | 219333 |
rs762259130 | in-del | -/AA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167244 | TCCAGCCTGGGCAAC[-/AA]GAGTGAAACTCCGTC | 219333 |
rs762259942 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27074317 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 219333 |
rs762266669 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167731 | CCACCCTATTTCTTG[-/A]GAAGGAAAAAGAAAT | 219333 |
rs762308923 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136734 | CTTGATATATGCATT[A/T]TATGGTCCATATGCT | 219333 |
rs762320299 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132363 | TTAGTTACACATGTT[-/A]AAAAAATGTATAGGT | 219333 |
rs762355410 | snp | A/G | 4.9736e-05 | 0.00498653 | intron-variant | USP12 | GRCh38.p7 | 13:27089969 | GTTGCTGAAACCCCT[A/G]TGTGAAATTCAAAAC | 219333 |
rs762387063 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123631 | CTTCTTGTGATAGTG[A/G]ATAAGTCTCATGAGA | 219333 |
rs762422535 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150907 | ACAAAAAACTAACTC[C/T]AAACAGATCAAAGAA | 219333 |
rs762423273 | snp | C/T | 1.71849e-05 | 0.00293124 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171666 | CATCTTCCACCCAAT[C/T]ACAGCGGCGGCGGCG | 219333 |
rs762432866 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116995 | TCCCCATCGTTACAC[-/AT]GATCGTATTTTCATA | 219333 |
rs762439195 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27116088 | GAGGCTGAGGTTGGC[A/G]GATCATGAGGTCAGG | 219333 |
rs762456400 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152072 | AACATAAAATGGTCC[A/G]TCTCTGGAAAACAGT | 219333 |
rs762469233 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163036 | AGTTTTAACAACCCA[C/T]TGAACTGTCCTTGTA | 219333 |
rs762539602 | snp | C/G/T | 3.3145e-05 | 0.0040708 | intron-variant | USP12 | GRCh38.p7 | 13:27069429 | TAAATGAGCTCTGTA[C/G/T]AGCCAGAATGGCTTA | 219333 |
rs762550105 | in-del | -/AA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133628 | CAAGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 219333 |
rs762590351 | snp | A/C | 1.67781e-05 | 0.00289634 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171644 | AGGATTTCCATCCGG[A/C]CAGCGCCATCTTCCA | 219333 |
rs762625503 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27090818 | CTCAGTTAAGCAAAT[G/T]CTTTCCCATTTTAAT | 219333 |
rs762629682 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27104763 | GTGTACAGTGTCAAC[C/T]GACTAATTTAAAGGC | 219333 |
rs762638332 | snp | A/C | | | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169317 | ACACACACTCGCCAG[A/C]CAAGAAGGATACGGG | 219333 |
rs762687274 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27087631 | ACAACTGTACAAGGT[-/C]CCTAGTTTATTGTTT | 219333 |
rs762718560 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27095314 | CTATGAGATTATGTC[A/G]TAAGACATAATTTCC | 219333 |
rs762755639 | snp | C/G | 1.76752e-05 | 0.00297276 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116612 | CTATAAAATGAAAAA[C/G]AAAAATCTTAGTATT | 219333 |
rs762767175 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128988 | TAGTTTAATAGTAAC[A/G]GAGTTCATACTCCAG | 219333 |
rs762810993 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130148 | GCTGCCTAGTAACAG[A/G]GCTGGCAGCGGGAAC | 219333 |
rs762811944 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27081432 | GCAATTCAGTCAGAT[C/T]GTCAGGATCCTCTTC | 219333 |
rs762823573 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27111832 | TGAGTATTTTTGTAA[A/G]GGCTTTAGATTTTAA | 219333 |
rs762830461 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27103763 | AAAAAAAAAAAAAAA[-/G]AGAGAGAGACAGAGA | 219333 |
rs762886049 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27114807 | TGAGCAATATAGCAA[C/G]ATCCCATCTCTACAA | 219333 |
rs762900964 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133198 | TATCCTCTAGCTCTA[C/T]TCCAGTTCAATAAAC | 219333 |
rs762905607 | in-del | -/AT | | | intron-variant | USP12 | GRCh38.p7 | 13:27070442 | GACATGGGGGGACAC[-/AT]GTATAAAAATTCATC | 219333 |
rs762917847 | snp | A/C | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068605 | TACCAGTTTTAAGTA[A/C]AATAAATAAGGAAAA | 219333 |
rs762957609 | snp | C/T | 1.6797e-05 | 0.00289797 | intron-variant | USP12 | GRCh38.p7 | 13:27116499 | ATGATTCTAAAAGCG[C/T]ATCAATGGATACTTA | 219333 |
rs762962019 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27114881 | TGGTCCCAGCTACTC[A/G]GGAGGCTAAGGCAGG | 219333 |
rs762976048 | in-del | -/AT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143698 | GCCATCATGTTCCAC[-/AT]GATAACCTGCAATAT | 219333 |
rs763009245 | snp | C/G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27082616 | ATCTTGGCTTTCAAC[C/G/T]TGCCCTATTCATTAA | 219333 |
rs763083276 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154190 | TCTTTTAATGAAGCC[A/G]AACCATCATTTAAAT | 219333 |
rs763101037 | in-del | -/AT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129116 | TAAAAAAAAGTACTC[-/AT]ATATTGTGAACTATC | 219333 |
rs763135182 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132036 | TCTACATCTAAATCT[G/T]TAGCTAGATTTACCA | 219333 |
rs763151630 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27099252 | TACTGAAATGTTATT[A/G]TAAGAATGTATGCAT | 219333 |
rs763186892 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27071597 | AAAGATCCAATATGA[C/T]GCTTGAAACAGGCAA | 219333 |
rs763222198 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27077541 | AGAATATGAATCCTA[C/T]TTGCCAAAGATCCTC | 219333 |
rs763266095 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166653 | ACCATAATATTTATA[C/T]ACATGCCACATAATT | 219333 |
rs763283999 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27106205 | AAAAAACAAGATCCC[A/C]TGAAACGTTACATGA | 219333 |
rs763286679 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27074740 | CAGAAAGCAAAATTG[G/T]CTAATAAGAAATGAT | 219333 |
rs763345678 | in-del | -/G | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173094 | ATTATAAGCTTGCTT[-/G]GGGGGGGGAATGCAG | 219333 |
rs763355024 | snp | A/G | 1.64885e-05 | 0.00287123 | synonymous-codon, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105834 | TGCTAAGCATGTAAG[A/G]AGGCTCTCCTTTTTC | 219333 |
rs763440245 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145692 | ATCTAGTTGTTTCAT[A/G]AAGTTGTTTATCTAG | 219333 |
rs763445638 | in-del | -/AAA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144500 | GGCAAGACTCTCTTT[-/AAA]AAAAAAAAAAAAAAA | 219333 |
rs763450730 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123763 | AGGCCTCCCCAGCCA[G/T]GTGGAAATGAGAGTC | 219333 |
rs763494017 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152941 | AGCGAGACTCCGTCT[-/C]AAAAAAAAAAAAAAA | 219333 |
rs763559441 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27111619 | AACAAACATCCCACC[A/G]CAAGTATTTTTTATA | 219333 |
rs763600801 | snp | A/C | 1.65957e-05 | 0.00288055 | intron-variant | USP12 | GRCh38.p7 | 13:27089980 | CCCTGTGTGAAATTC[A/C]AAACAAATTTATTTT | 219333 |
rs763602132 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134008 | GGGCATGCCCATTAG[C/G]TGGTACATGCCTGTA | 219333 |
rs763645273 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27100800 | CCTAGAGGAATCTAA[A/G]AAGAAGAATAATCAG | 219333 |
rs763678265 | in-del | -/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138980 | AACGGTAAGGTGTAT[-/G]ATCATTCAGCCTTAC | 219333 |
rs763683469 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159516 | ATCCAGCCTTCTCTA[G/T]CAATATCCAGTAACA | 219333 |
rs763688498 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27112397 | CTCAAGATCCTCCCA[A/C]CTCAGTCTGTGGAGT | 219333 |
rs763696924 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27079621 | AGACCCTGGAATCCA[G/T]TGGAATCTGAACTGT | 219333 |
rs763714086 | in-del | -/AAAC | | | intron-variant | USP12 | GRCh38.p7 | 13:27113270 | TCAAAACAAAAACAA[-/AAAC]AAACAAACAAACAAA | 219333 |
rs763726818 | snp | G/T | 1.67632e-05 | 0.00289505 | intron-variant | USP12 | GRCh38.p7 | 13:27116501 | GATTCTAAAAGCGTA[G/T]CAATGGATACTTACA | 219333 |
rs763793595 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147900 | TGGGAGGCTGAGGAC[A/G]GAGGATCACTGGAGC | 219333 |
rs763825861 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068233 | TTAGAATACTTAAGA[A/G]TTCTAAAGATTGGTA | 219333 |
rs763877977 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146999 | ATGCCTGAGGCTGCC[A/G]GAAGCAAGTAGAGAA | 219333 |
rs763914904 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27106103 | TTAAAATACAACTCT[C/T]AAAAATTCTTTGGAA | 219333 |
rs763921733 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27078269 | TTAAAAAAATACAGT[G/T]TAACAACTACTTATA | 219333 |
rs763954020 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171015 | GAGGAAATCTGCACT[C/T]GACTTCCGTCCTCTC | 219333 |
rs764001568 | snp | A/G | | | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125548 | GAGATCGATGCAGAA[A/G]GCGGGTGATTTCTGC | 219333 |
rs764026298 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27070853 | CCACCGCACCTGGCC[C/T]CCCTTGTTTTATTCT | 219333 |
rs764087757 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139844 | CTATGCTAAGGACAG[G/T]TGATACAAAGTTATG | 219333 |
rs764091260 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142910 | CCATCCTGGCCGACA[C/T]GGTGAAACCCCATCT | 219333 |
rs764113472 | snp | A/G | 1.83343e-05 | 0.00302768 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116622 | AAAAACAAAAATCTT[A/G]GTATTTATAGTAGTC | 219333 |
rs764137645 | in-del | -/TTTTTTTTTT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155090 | TTTTTTTTTTTTTTT[-/TTTTTTTTTT]GAGACGGAACCTCGC | 219333 |
rs764167026 | snp | C/T | 1.65745e-05 | 0.00287871 | missense | USP12 | GRCh38.p7 | 13:27095735 | GACCATTTTGTTTTT[C/T]CTGCTTTCTCTCTTC | 219333 |
rs764178217 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27095436 | CAATAAGCAACATTA[C/T]ATTAAGAATACAGAC | 219333 |
rs764179857 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27109446 | ATGAAAGAGACAATA[C/T]CACAAAGAAGGAAAA | 219333 |
rs764219637 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076024 | GACAGAGCAAGGCTC[C/T]GTCTCAAAAAAAAAA | 219333 |
rs764231212 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162142 | AATGACCATGTAAGG[G/T]TGATGTTGATATGTA | 219333 |
rs764240606 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166696 | AAAACTAGAGTTTTC[-/A]AAGCATATTAAAAAT | 219333 |
rs764243007 | snp | A/C | 1.67826e-05 | 0.00289673 | intron-variant | USP12 | GRCh38.p7 | 13:27105700 | TTTAACCTTCCTAGT[A/C]TGTCATTAATACAGT | 219333 |
rs764246482 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157248 | CTAGAAAACCACTTC[C/T]GATCCCTTTTTGCTT | 219333 |
rs764273881 | in-del | -/AACA | | | intron-variant | USP12 | GRCh38.p7 | 13:27111604 | TCTTCTCCAAACCTT[-/AACA]AACATCCCACCGCAA | 219333 |
rs764286824 | in-del | -/TAATAAAG | 1.64814e-05 | 0.00287061 | frameshift-variant, utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069366 | GTAGAATTCTTCAAT[-/TAATAAAG]AGCTTGTGCATCTAT | 219333 |
rs764504408 | snp | A/G | 1.6517e-05 | 0.00287372 | synonymous-codon | USP12 | GRCh38.p7 | 13:27075310 | GTAAGAGAGTTTTGT[A/G]TATCGATGAAGTTGA | 219333 |
rs764509714 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27089409 | TTCTGAGTTTGAGAC[G/T]GTTTCAAAATAAGAA | 219333 |
rs764526664 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135331 | TTTGATCTCAAATCT[C/G]TATCGTAACAACATT | 219333 |
rs764604750 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068014 | AGATTTGTAAAGGTG[A/G]GGGGAAGGGAAGGAA | 219333 |
rs764670049 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161807 | GGATAGCTTGAGCCC[A/G]GGGGGCAGAGGTTTC | 219333 |
rs764691795 | snp | A/T | 2.67476e-05 | 0.00365692 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171653 | ATCCGGCCAGCGCCA[A/T]CTTCCACCCAATCAC | 219333 |
rs764723822 | snp | C/G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27120470 | CCAGCCTGGCCAACA[C/G/T]GGTGAAACCCCATCT | 219333 |
rs764734136 | snp | A/G | 8.08865e-05 | 0.00635899 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171568 | GGTCCCGGCAGCCCC[A/G]GCCGCCCGCTCGCCG | 219333 |
rs764744633 | snp | C/T | 3.17667e-05 | 0.00398527 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171579 | CCCCGGCCGCCCGCT[C/T]GCCGCCACCTACCAT | 219333 |
rs764823501 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101100 | AAAATACCTCCAATG[A/T]CTTGAATGCTCTGGA | 219333 |
rs764836389 | in-del | -/TGTGTGTGTGTGTGTG | | | intron-variant | USP12 | GRCh38.p7 | 13:27087252 | TATAGTGGGGAGGGA[-/TGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 219333 |
rs764837956 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27097986 | ACTTTATATAGTACT[-/T]TTTTTTTTTTTTTTT | 219333 |
rs764853221 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148193 | ATGCTAACAGACATA[C/T]CTTACAAGAAATACT | 219333 |
rs764947639 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141814 | AATGTTCCAAAATCT[G/T]ACTTTTTGAGTGCTA | 219333 |
rs764961416 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136757 | CATATGCTCAGGGAG[A/C]ATTCAGTATAAAAAA | 219333 |
rs764962303 | snp | A/C | 1.64931e-05 | 0.00287163 | synonymous-codon | USP12 | GRCh38.p7 | 13:27075286 | AAGTTCTAAAGGAAA[A/C]ACTACCCGGTAAGAG | 219333 |
rs764990027 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27088734 | CTTTTGTGACTCCAC[C/T]GGGGCACTGACTTCT | 219333 |
rs765053328 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135510 | TTGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGCC | 219333 |
rs765057720 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27095154 | AATTTTCAAGCTTCA[A/T]CTTTACAAAGTGTCC | 219333 |
rs765059747 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27079948 | GGGGGTCAGGGCAAA[C/T]AGAATGCTTTATGTG | 219333 |
rs765130380 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27073583 | TCAGCTCAGTATATT[-/G]TGAGTAGAGCAATTC | 219333 |
rs765134384 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143216 | TGTAATTGATTATTA[C/T]CAAACAACTAAACAC | 219333 |
rs765138303 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159679 | TTATCATTGTGAGAT[C/G]TGAATCTGTGAAATG | 219333 |
rs765146234 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127668 | TTTCTGGCAAGTTCT[C/G]AAAAACTGAATTTCT | 219333 |
rs765147483 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27093959 | TATGATTTCAACTAC[A/T]CAATATTCTGGAAAA | 219333 |
rs765198035 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128769 | TAACAGATTTCTGTG[A/G]TTATGCTCAGTGAGA | 219333 |
rs765255895 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27081312 | CCATTTCAACAATGT[A/T]CACAGCATGTTAACC | 219333 |
rs765258225 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27084604 | ACTTTATTCTTTTTC[A/G]TGTGGATATTCAGTT | 219333 |
rs765281543 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27081037 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 219333 |
rs765329399 | in-del | -/AGAG | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136876 | GGGAAGGTTTAAGTT[-/AGAG]GGAGTAAAAAAGACA | 219333 |
rs765338446 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164616 | ATAAATGTATATAAA[C/T]TGCCACTCTAACCTC | 219333 |
rs765348236 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27098169 | TCAAAAAGTTTCAGA[G/T]TTCTGGATTACGGAT | 219333 |
rs765373965 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147067 | GCATGGTCCTGGTGA[C/G]ATGCTGATTTTGGAC | 219333 |
rs765419572 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27120718 | CAAATGGAAGAAGAC[-/A]TTTTTTTCTGACTTC | 219333 |
rs765503646 | in-del | -/T | 2.7782e-05 | 0.00372696 | intron-variant | USP12 | GRCh38.p7 | 13:27105964 | ACAGAAAAAAAAAAG[-/T]TTTTGTTAAATTTAG | 219333 |
rs765506503 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27069808 | CAAAATTAGCTAGGC[A/G]TGTTGGCGCATGCCT | 219333 |
rs765523859 | snp | A/G | 0.000443424 | 0.0148834 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117837 | GCACCTGTGGTCCCC[A/G]ACGACCATGTGAAAG | 219333 |
rs765543689 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163431 | ATTTTGCAAAGTTCA[A/G]CTCTCTTCTAAGAAG | 219333 |
rs765553890 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131763 | AAGAGGGTGTAAAAC[G/T]CAAAGTATTATTCAC | 219333 |
rs765572771 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27074357 | CTGAGCCGAGATGGC[A/G]CCACTGCACTCCAGC | 219333 |
rs765610813 | snp | C/T | 9.94843e-05 | 0.00705211 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116582 | CTCTTTCTCTAATGC[C/T]GAAGCATTGGCGCCC | 219333 |
rs765616216 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144297 | CAGCCCAGTTTGAGA[A/C]CACCTGGGCAACACA | 219333 |
rs765639530 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123658 | GAGATCTGATGATTT[C/T]ACAAAGGGCAGTTCC | 219333 |
rs765640611 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133629 | AAGACTCTGTCTCAA[-/A]AAAAAAAAAAAAAAA | 219333 |
rs765652753 | snp | C/G | 1.7741e-05 | 0.00297829 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117805 | CAGTTTCAAGAACGT[C/G]ATCAACTCAATTCTG | 219333 |
rs765656960 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27110680 | AAATGTAACTACAGA[C/T]ACACTTCAATGAACC | 219333 |
rs765666699 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27121980 | ACTCTAAGCAGACTT[C/T]TAAAAAGAACTAAAT | 219333 |
rs765677514 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27076100 | ATTCCTTTGGACTTG[C/G]GTAGACTGAAATCTA | 219333 |
rs765686876 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27090782 | GGAGATACGTCTGAC[C/T]CAGCAACCTGTGCCT | 219333 |
rs765808910 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27090833 | GCTTTCCCATTTTAA[G/T]ACATCAAAATTATTA | 219333 |
rs765911871 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157558 | TATAAGTTTATAGAA[C/G]ATTTTTCCCTAAACC | 219333 |
rs765912823 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168067 | CCATGCTCAGGGTGC[A/T]GTGCTAGGCACAGGC | 219333 |
rs765915633 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164669 | GATAGCAAATGGTCA[A/C]ATGTTATATGTAAGT | 219333 |
rs765987177 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27103797 | AAGAGATGAAAAAAG[-/A]AAAAAAAGCCCATTT | 219333 |
rs766005158 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27091740 | AAACCCTGGGGAACA[A/C]CCACATTTAAAGAAT | 219333 |
rs766012956 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138167 | GAGTTCACTTCAGCT[A/G]CTCAATTTGTGATAA | 219333 |
rs766090314 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128992 | TTAATAGTAACGGAG[C/T]TCATACTCCAGATTC | 219333 |
rs766100099 | in-del | -/AA | | | intron-variant | USP12 | GRCh38.p7 | 13:27116313 | CAAGACGCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 219333 |
rs766106094 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123867 | ACATAGGCAATGGGG[C/T]AAGTATCTCCTTTAA | 219333 |
rs766109391 | snp | A/G | 0.000115341 | 0.00759324 | synonymous-codon | USP12 | GRCh38.p7 | 13:27075256 | GGTGGCATCACCTGA[A/G]GTGTTAAACAGACGA | 219333 |
rs766162162 | in-del | -/CTA | | | intron-variant | USP12 | GRCh38.p7 | 13:27112104 | CTGAAACCAAACTGT[-/CTA]CTAGGTTCAAGTCTG | 219333 |
rs766225217 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27089316 | CTATTAAAGTGCCGG[A/G]GCCATGAGGTACATA | 219333 |
rs766237784 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066829 | AACCAACATACAACC[C/T]CACGATGCTTTCTTC | 219333 |
rs766243884 | in-del | -/AAC | 2.24288e-05 | 0.00334872 | intron-variant | USP12 | GRCh38.p7 | 13:27075409 | AAAAATAAAAATGAA[-/AAC]AAAATTTCATAAAAG | 219333 |
rs766273756 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27102604 | CCTACTGATGGTAAC[A/G]TTTTTGCCTCAGATC | 219333 |
rs766286579 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27114907 | GCAGGATTGCCTGAG[C/T]CCAGGAGGTGAAGGC | 219333 |
rs766297677 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150915 | CTAACTCCAAACAGA[C/T]CAAAGAAGTACATAA | 219333 |
rs766310899 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27105337 | TGACATGCTCTCTAT[A/C]TAAGGCTACTGCAAG | 219333 |
rs766356733 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27087222 | AACAAAAGGTGCACC[A/G]ACCAAATAAGTAAAT | 219333 |
rs766408525 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27071971 | ACAAATTATTCTTTA[C/T]GGTGAACACTATTTT | 219333 |
rs766432242 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068656 | TCTTTCCCCTTGGGG[A/G]AACAAAAAGCCACTT | 219333 |
rs766449530 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133219 | TTCAATAAACTTAAC[A/G]CAAACACCACACTCA | 219333 |
rs766592246 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27106154 | TATCAGGTTCTTAGG[C/T]ACATCCAAATTAAAA | 219333 |
rs766601939 | in-del | -/TTTC | | | intron-variant | USP12 | GRCh38.p7 | 13:27170213 | CATCCTTCAATATGA[-/TTTC]TTTAATACTGTCGAT | 219333 |
rs766622903 | in-del | -/AAC | | | intron-variant | USP12 | GRCh38.p7 | 13:27097469 | AAACTCCATCTCAAA[-/AAC]AACAACAACAAAACA | 219333 |
rs766667707 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154219 | ATTACTATGCTGTAA[A/C]TATAAAAGGTTCTGA | 219333 |
rs766684924 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27078840 | GAAAATATGAACACC[C/T]TAACTATGGACTTAA | 219333 |
rs766742279 | in-del | -/AAC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150047 | AGGGTGACTATAATT[-/AAC]AACAATTTATTGTAT | 219333 |
rs766744363 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144662 | GTAACAATCAAAAGC[A/G]TAAACCTAGATGGAA | 219333 |
rs766751872 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166739 | CAAGTCTTATCTTTG[C/T]GATAACTAAGTGCCT | 219333 |
rs766793092 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27111885 | ATGTTCAGTTATTTG[A/G]ATATGTGGTTTTAAT | 219333 |
rs766806886 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27077885 | GGTTACATTAGGGAG[A/G]TCTTGATCACTGTCA | 219333 |
rs766850603 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132078 | GCACGTAAGAAATCC[A/G]GGCTATGAAACAAAA | 219333 |
rs766940664 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145707 | AAAGTTGTTTATCTA[A/G]TTGTCCTAAAGTCCC | 219333 |
rs766953176 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168840 | CAATTAAGGTATTGC[A/C]GATTTGCCCAGGTAC | 219333 |
rs767016095 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139720 | AAATTCTTTCATGTA[C/T]AAATAAATGCAGGTG | 219333 |
rs767031088 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148606 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 219333 |
rs767042429 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27109225 | TCAAAGCATTAGGTT[A/G]AAAGTTGATGGGGAT | 219333 |
rs767050568 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161544 | AATTTTATACCTTTA[-/A]AAAAAAATGTTACTA | 219333 |
rs767055879 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124205 | AAAAGTAAACTAACA[A/G]CCAGGAATGTTTTCA | 219333 |
rs767100752 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27070195 | TGAGTGAATAAAGTC[-/T]TGACACAAAAGAAAT | 219333 |
rs767102899 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27091964 | ACTATTCTCTGGCTG[G/T]CATGGCATCCTGTGC | 219333 |
rs767108556 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170757 | CCTAGCTCCAGCCAC[A/G]TACAGATGTGTCTGG | 219333 |
rs767151163 | snp | A/G | 1.98671e-05 | 0.00315169 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116647 | GTAGTCATGCACCAC[A/G]TAATGACACTTCAGT | 219333 |
rs767154354 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159037 | TCTTTCTAGCAATTA[C/T]TTCTTGGGAAAGGGC | 219333 |
rs767156881 | snp | A/G | 1.6486e-05 | 0.00287102 | missense, utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069374 | TCTTCAATAGCTTGT[A/G]CATCTATTTTCTGTG | 219333 |
rs767164252 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27081935 | AGTAAATTATGCTAT[A/C]AACAGGTGTGCTGTC | 219333 |
rs767201551 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163379 | CTATTTACATCTGGT[A/G]TCCCATCCCTCCATG | 219333 |
rs767228476 | in-del | -/CAG | 9.83978e-05 | 0.0070135 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171667 | TCTTCCACCCAATCA[-/CAG]CAGCGGCGGCGGCGG | 219333 |
rs767237379 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27084497 | AGAGACAGTGAGATG[-/A]AAAAAAAAAAAAAAA | 219333 |
rs767254270 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27106777 | GAAGAGGAAAAATAA[C/T]GGAGAGATGGATAAA | 219333 |
rs767274672 | in-del | -/AAAT | | | intron-variant | USP12 | GRCh38.p7 | 13:27122653 | TGAGACCCCATCTCA[-/AAAT]AAATAAATAAATAAA | 219333 |
rs767339427 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173295 | CTACATCTTAGACCT[C/G]TAGGGCCTACCTGGG | 219333 |
rs767350653 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27090908 | ACAACATGTGACTAT[A/C]CAAAGTATGTATTTA | 219333 |
rs767376812 | in-del | -/AA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144501 | GCAAGACTCTCTTTA[-/AA]AAAAAAAAAAAAAAA | 219333 |
rs767483233 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27104939 | AGCCAGAATTCTACA[A/T]GTTATCTAAATTCCA | 219333 |
rs767513869 | snp | A/C | 1.65173e-05 | 0.00287374 | missense, intron-variant | USP12 | GRCh38.p7 | 13:27071124 | GACTCTTAACTATTG[A/C]AATATAATGGCCTCG | 219333 |
rs767534644 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27072965 | ATTAGTCTTTTATTA[G/T]TGAGCAAATTATTTT | 219333 |
rs767569088 | in-del | -/CA | | | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168993 | TTCTCTCCACCATTC[-/CA]CACACACACAGCCAC | 219333 |
rs767581086 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27107564 | TCTGTGTGCATGCAT[C/G]CATGTTTGTGTGTAC | 219333 |
rs767612839 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27120362 | GATGGTGAGTTAAGT[C/T]CTGCTCCAGGCCAGG | 219333 |
rs767662437 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27097574 | AGGGCACAGCTGCTA[C/G]AGCAAGGCTGTCTGG | 219333 |
rs767711020 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143990 | GGAAGGATCACTTGA[A/G]GTCAGGAGTTCGAGA | 219333 |
rs767720928 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27083558 | CCTATATGCTTTAAC[C/G]TCCCATGGGATAAAC | 219333 |
rs767847052 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27075896 | ATAGCCGGGCATAGT[G/T]GCAGGCGCCCATAGT | 219333 |
rs767884150 | snp | C/G | 1.75385e-05 | 0.00296124 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171673 | CACCCAATCACAGCG[C/G]CGGCGGCGGGCGGGG | 219333 |
rs767887960 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156291 | AGAAAACACAAAGGA[C/T]GGAAGAACATGTTAA | 219333 |
rs767937579 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146897 | TATGACTGGCATCCT[G/T]CTATTATAAAAAAGG | 219333 |
rs767985540 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135114 | ACATGGTGAAAGCCC[A/G]TTTCTACTAAGAAAA | 219333 |
rs768021194 | in-del | -/GT | 0.000165089 | 0.00908389 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069259 | GAAATGAGGCAGAAA[-/GT]GTCTCTTCATCACGG | 219333 |
rs768075514 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133497 | GCCGGGTGTGGTGGC[A/G]GGCACCTGCAGTCCC | 219333 |
rs768097953 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143324 | GTAGGGAGTATCACA[C/T]TGATTCCTTATTCTG | 219333 |
rs768098167 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128445 | CAATACAAAAAACTT[C/T]CAAAAAATTAATAAA | 219333 |
rs768101724 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27095081 | GATTGCTTGAGCCCA[A/G]GAAGTCGAGGCTACA | 219333 |
rs768122920 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27087448 | GGTGGTGGCTACAAG[A/T]TTATCACTGTGTATT | 219333 |
rs768135086 | snp | C/T | 5.00697e-05 | 0.00500323 | intron-variant | USP12 | GRCh38.p7 | 13:27090175 | TGTAAAAACAGTGAA[C/T]TGTCTTTGATTTTTT | 219333 |
rs768191624 | in-del | -/A/AA | | | intron-variant | USP12 | GRCh38.p7 | 13:27098365 | AATATACAGAATATT[-/A/AA]TAAAAAAAAACCCTT | 219333 |
rs768195817 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27075551 | TATTTTTATACTGAC[-/A]AAACAACATTCTGAA | 219333 |
rs768215879 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145990 | ACAACAATACCAGTT[A/G]CAGGTAATTATTAAT | 219333 |
rs768331317 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27108999 | TGACATTTTTTTAAA[A/G]AGCAGCCCTCTTTAG | 219333 |
rs768348528 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27114585 | TGTATTATACAAATT[A/G]TAGTGACAGGTAATT | 219333 |
rs768370778 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27082036 | TTTAGGGATGGTAAA[G/T]GAATACTGGCTTCAA | 219333 |
rs768374496 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161625 | GCAGTGGTTCACACG[G/T]GTAATTGCAGCATTT | 219333 |
rs768392991 | snp | A/G | 1.67217e-05 | 0.00289147 | missense | USP12 | GRCh38.p7 | 13:27095665 | ATCTCATGAACCCAC[A/G]TTGGGTCTGGTGTGC | 219333 |
rs768394165 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27072698 | AAGACAGGAGGTAGA[A/C]GGGAGAGAGGGATGG | 219333 |
rs768431935 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27120112 | GAAAGTCAAAATTTT[A/G]CTGTATGATTGTTAC | 219333 |
rs768446887 | snp | C/T | 1.7742e-05 | 0.00297837 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117780 | TCGCACAGACAATCA[C/T]AGCGTGTCACAGTTT | 219333 |
rs768452287 | snp | C/T | 1.65586e-05 | 0.00287733 | missense | USP12 | GRCh38.p7 | 13:27090151 | AAATCTTCATCTTTG[C/T]TGCTTATCTGTAAAA | 219333 |
rs768459329 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156114 | GAAGAGTCATTCTGA[C/G]AATGCCAGCCTCATC | 219333 |
rs768511665 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166566 | ACTTTGAGACCTATT[A/G]GCCACTTATTAGCAA | 219333 |
rs768519965 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134564 | ATATTACAAAATATA[C/T]TCTCTCAATTACTTC | 219333 |
rs768553371 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124806 | TAAATGAGAAAGGGC[A/G]AAGAGTCAAAGAGAA | 219333 |
rs768594808 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27119084 | TAAGGCAGCTGGTGG[C/T]GCCTGGCACACAAGC | 219333 |
rs768644891 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127194 | CATAGTTTTTAACTA[C/T]CCCATCAAAGTTAAA | 219333 |
rs768654526 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27110503 | CAACTTTTTGAAGAG[G/T]CTTGTGAGATCCAAC | 219333 |
rs768722628 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134098 | GCAGTGAGCTATGAT[C/T]AGGCCACTGCACTCC | 219333 |
rs768739447 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145164 | TTTCCTTCCAAATCG[C/T]AGGTCTCCTCAACTA | 219333 |
rs768804373 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27123476 | AATAGCCATCCAATA[C/T]TAAGAATTTGTAGGC | 219333 |
rs768811329 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27077162 | GGTGACATAAGAAAA[C/T]ACTTAAGAAGTCAGG | 219333 |
rs768828938 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158076 | AGTCTTAAGCCCCAA[A/T]ATCTCAGAATATGAC | 219333 |
rs768845510 | snp | C/T | 4.36824e-05 | 0.00467325 | intron-variant | USP12 | GRCh38.p7 | 13:27105985 | TTAAATTTAGGGCAA[C/T]ACATTTTCAAGAGAG | 219333 |
rs768854462 | in-del | -/T | 1.6518e-05 | 0.0028738 | frameshift-variant, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105876 | CTTATACGCAAGAAC[-/T]TTTTCCCGAAATGGA | 219333 |
rs768861642 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27103151 | AAAATTTTTAACATA[C/G]TATGGCAGGAAATTA | 219333 |
rs768882564 | snp | A/C | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069095 | AGCATGATACCTGAG[A/C]AAATAAATCAACTAC | 219333 |
rs768899332 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27091237 | GGGTGACAAGAGATA[C/G]TATGGCAGAGGTAGG | 219333 |
rs768902392 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158612 | GTACTGGATCCTGTA[A/G]GTAACTGTAACACAA | 219333 |
rs768928727 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27105407 | AATGCATAAGCATGC[-/A]AAAAAAAAAGAAACA | 219333 |
rs768989049 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27080569 | CACACGGAATAAAGG[G/T]AGAGTAAAGAGACTT | 219333 |
rs769039739 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132208 | ATAATTATATCTTCC[A/G]TGCTTTATCTTTGGT | 219333 |
rs769079409 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067883 | GCATGGAAAAACGTC[C/T]AAAAAAACTGCAATC | 219333 |
rs769112049 | snp | C/T | | | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27169070 | TTTGGAAAACTTTTA[C/T]ACTGAATGCAGAACT | 219333 |
rs769148402 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150367 | ACAAAAAAAGAGAAT[A/G]ACATATAAAAGAAAA | 219333 |
rs769193530 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116701 | GTCCTATCACATTAC[A/G]ATGGAGCTGCCCTAC | 219333 |
rs769193729 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27088371 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 219333 |
rs769194473 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27104592 | CAAGATGTATTTTTA[A/T]GAGCAATTAATCAAA | 219333 |
rs769239299 | snp | C/T | 0.00016503 | 0.00908228 | synonymous-codon, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116546 | ATAGTGCTCATTGAC[C/T]GGAAACTGTTCTGGA | 219333 |
rs769241282 | in-del | -/AA | | | intron-variant | USP12 | GRCh38.p7 | 13:27091163 | AGACAACTCAGAGAG[-/AA]AAAAAGAGGACATGA | 219333 |
rs769278650 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164182 | GCAACAGTACTCTAA[C/T]TCTACTGAAAGATAT | 219333 |
rs769297637 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27090544 | ATATCTGTATTGTCA[C/T]TAAAAAAAAAATTTA | 219333 |
rs769300970 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27114228 | TGAAAAAAAAGCTAT[A/T]CAAAAAAATGCACAG | 219333 |
rs769344884 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151534 | TGCCTGTAATCCCAG[A/T]GCTTTCGGAGGACTA | 219333 |
rs769350596 | snp | C/T | 2.56007e-05 | 0.00357766 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171641 | ATTAGGATTTCCATC[C/T]GGCCAGCGCCATCTT | 219333 |
rs769381615 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27083549 | CTCCTCTCACCTATA[C/T]GCTTTAACCTCCCAT | 219333 |
rs769433000 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27103278 | AAGATATGCAATGAA[C/T]AATATATTAAATCCT | 219333 |
rs769433421 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117220 | GAATTACATTCATAA[C/T]ATGTTCTTTTTTTCT | 219333 |
rs769468591 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151931 | CATCAGAGAAATGCA[A/G]ATCAAAACCACAATG | 219333 |
rs769471596 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27097578 | CACAGCTGCTAGAGC[A/G]AGGCTGTCTGGGTTG | 219333 |
rs769528413 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27099226 | TCAGGGAAACTTCTA[G/T]GTTTGTTTGGTACTG | 219333 |
rs769554767 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | USP12 | GRCh38.p7 | 13:27075222 | CAACAGCAACAAGGT[C/T]GTACATTCTGTCTGG | 219333 |
rs769568674 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27109290 | GCGATTTCAGCATTG[C/T]TCAAGTGAACAACTG | 219333 |
rs769659826 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131044 | GCTGAATGACACTCA[A/G]AGTTTATGTGTGGCA | 219333 |
rs769679875 | in-del | -/TAGA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137972 | GAACCAGAAAAAGCC[-/TAGA]TAGAGCCTTCACTTA | 219333 |
rs769695565 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156678 | ATACAAAAATTAGCT[C/G]GGCATGGTGGCAGGC | 219333 |
rs769771136 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167274 | TCTCAAAAAAAAAAT[-/A]AAATAAATAAATAAA | 219333 |
rs769771864 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101323 | TCAGGACAATCCCTG[A/T]GAACTGTATTATATT | 219333 |
rs769847418 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27099176 | TATTTCAAAGGAAGA[C/T]GAGATTGAGGAGCTG | 219333 |
rs769869166 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158714 | ACACACAGTTTCTGG[C/T]ACTTTGTTATGGCAG | 219333 |
rs769895042 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27100527 | CTCCTCATCCACTGA[C/T]GGCCTGATTCAGTTT | 219333 |
rs769913988 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27107714 | GCTGATACAAGATCT[A/G]CGATAAGAAATGTAC | 219333 |
rs769939604 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27111617 | TTAACAAACATCCCA[C/G]CGCAAGTATTTTTTA | 219333 |
rs769984676 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27078955 | CAATAAAGAAGTCTC[A/G]ATAAATTTCAAAGAT | 219333 |
rs770014665 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126049 | GGGGGCAGGGCATAT[A/C]TGAACAAAAGGCAGC | 219333 |
rs770054777 | snp | A/G | 3.30267e-05 | 0.00406353 | synonymous-codon, intron-variant | USP12 | GRCh38.p7 | 13:27071107 | CAACAACCAAAAATC[A/G]TGACTCTTAACTATT | 219333 |
rs770058125 | snp | C/T | 3.29875e-05 | 0.00406112 | intron-variant | USP12 | GRCh38.p7 | 13:27075170 | GGAATTCCACTACTA[C/T]GTCCCCGGAGTTGCA | 219333 |
rs770089046 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27082897 | CTGGAGTGCAATGGC[A/G]TGATCTCGGCTCACC | 219333 |
rs770125583 | in-del | -/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162609 | ATACCTCAAAAAAAA[-/T]CTATTGTTAATTTTC | 219333 |
rs770194065 | snp | C/G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27104665 | CAAACGTATCAAATT[C/G/T]AAGAATAATAGCCTA | 219333 |
rs770219243 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27077357 | GTGTCAGTGCACTAT[G/T]AATAAATGGCAGTCA | 219333 |
rs770221258 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162051 | TAACTTGTGAGCTCC[A/G]TTACAACTCCTACAG | 219333 |
rs770240952 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158164 | TGGACCCTAATCCAG[C/T]GTGACTGGTGTCTGT | 219333 |
rs770263532 | snp | A/C | 2.68086e-05 | 0.00366109 | intron-variant | USP12 | GRCh38.p7 | 13:27105963 | CAACAGAAAAAAAAA[A/C]GTTTTGTTAAATTTA | 219333 |
rs770274880 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172413 | TTTCTTTTTACGTAT[A/G]TTGGATGAATCACCG | 219333 |
rs770306378 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135304 | AAATGAAAACATTTA[A/G]AATTTATTTTGTTTG | 219333 |
rs770316088 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137842 | AGCAGACTTGCTCCC[C/T]GACTCCCTCATTGGC | 219333 |
rs770316652 | snp | G/T | 3.29717e-05 | 0.00406015 | synonymous-codon, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105828 | GAGATCTGCTAAGCA[G/T]GTAAGAAGGCTCTCC | 219333 |
rs770324285 | snp | A/T | | | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27065845 | GAGGAGGAGCAGGAG[A/T]AACAGTGATCTTTAA | 219333 |
rs770326190 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27093100 | ACTAGGGAGGCTGAC[-/A]CAAGAGAACCACTTG | 219333 |
rs770374337 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117544 | AACTAGGTTTACACA[C/G]AGAAACATGAGTATC | 219333 |
rs770401323 | in-del | -/TA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148378 | AACTGTATAAAACTA[-/TA]TATATATATATTATA | 219333 |
rs770411889 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27118821 | TAACAGGTGAAGGTT[A/C]TCTCTCTACTGTTAG | 219333 |
rs770423974 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27091474 | CGTTTATATTTGCGA[C/T]TGAGTTGGTGCCAAG | 219333 |
rs770439279 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164387 | TAAATAAAGCAAGCT[C/T]ACACATCTCTTCTTT | 219333 |
rs770466557 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154684 | GTAGTAGAAAAATAA[C/G]TGCCTCCCTCAAAAT | 219333 |
rs770488773 | snp | A/C | 1.70889e-05 | 0.00292304 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171556 | GCCCGCCCGAGAGGT[A/C]CCGGCAGCCCCGGCC | 219333 |
rs770603785 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27096348 | AACTCTGATGTAGAG[A/T]CAGGTTTAAGAATCA | 219333 |
rs770621293 | in-del | -/T | 1.67414e-05 | 0.00289317 | intron-variant | USP12 | GRCh38.p7 | 13:27090184 | GTGAATTGTCTTTGA[-/T]TTTTTTCAAATACTA | 219333 |
rs770679757 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153433 | TATAAAGTAATGAAA[C/T]AGAAATATTTTCTAG | 219333 |
rs770700388 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162408 | CTGTAGATGTCATAA[C/G]GAGTTTGCATGTCTA | 219333 |
rs770811375 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163316 | TTACTGTTCACAAGA[A/C]CCGCTTTCACGCCAA | 219333 |
rs770814516 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27077102 | AATTCAAACATAACC[A/G]AGTGTTGTACAACTT | 219333 |
rs770819681 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117340 | AACTAAATATAAATA[C/T]GCACATGCTCAGTGG | 219333 |
rs770849810 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143968 | CAGCACTTTGGGAGG[A/C]CAAGTTGGAAGGATC | 219333 |
rs770851832 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158041 | TGGGTGAACTGTGTT[C/T]CCTAATAAAGGTACG | 219333 |
rs770860424 | in-del | -/ATGTGTGTGTGTGT | | | intron-variant | USP12 | GRCh38.p7 | 13:27087251 | ATATAGTGGGGAGGG[-/ATGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 219333 |
rs770879332 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27101908 | CACGGCACATGAAAC[A/G]CTGCTTGTCCATGCA | 219333 |
rs770889159 | snp | C/T | 3.49815e-05 | 0.00418205 | intron-variant | USP12 | GRCh38.p7 | 13:27089871 | TAAAAATCCATAAAG[C/T]TCTAAAATTACCGTT | 219333 |
rs770894610 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27078072 | TTTCTATTTAAATTT[-/A]TTTTTTTAATGACAT | 219333 |
rs770907521 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147634 | AGTCAAAGACAAAAA[G/T]ACACAGCAAGAAAAG | 219333 |
rs770999509 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147657 | AAGAAAAGAGGATGC[A/G]TCACTTATAAGGGAA | 219333 |
rs771055439 | in-del | -/TG | | | intron-variant | USP12 | GRCh38.p7 | 13:27087101 | GAGGGGAAGGGGCTG[-/TG]TGTGTGTGTGTGTGT | 219333 |
rs771064514 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153632 | CCTTCCACAAGTCAC[C/T]CTCATGGAGCTCACA | 219333 |
rs771072514 | snp | C/T | 3.35666e-05 | 0.00409661 | missense, upstream-variant-2KB, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116593 | ATGCCGAAGCATTGG[C/T]GCCCTATAAAATGAA | 219333 |
rs771073660 | snp | A/C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27088794 | CTGTGTTTTGTATCC[A/C/T]GTCCCTGTAATAAAT | 219333 |
rs771098711 | snp | C/T | | | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27066009 | GAATGTTGTTTTACA[C/T]ACATGCAATTCTGTT | 219333 |
rs771107590 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136394 | TCCCAGCTACTCAGG[A/G]GGCTGAAGCAGGAGA | 219333 |
rs771188878 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27114202 | TAATAAAGAACCATA[C/T]AATAAAACAATGAAA | 219333 |
rs771199855 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134772 | TATAAAAAGACTAGG[A/T]CAGTAATTAATGATC | 219333 |
rs771227045 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141140 | TCTGCCCCAGCCTCC[A/C]GAGTAGCTGGGACTA | 219333 |
rs771244000 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127351 | AGATATATGGTACCA[A/G]TGACATAAAAGGGAA | 219333 |
rs771252250 | snp | C/T | 1.68425e-05 | 0.00290189 | intron-variant | USP12 | GRCh38.p7 | 13:27071038 | AACATATGCATACAA[C/T]TTTCAAAAATAAGAA | 219333 |
rs771295176 | in-del | -/TA | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124471 | TTTAAATAGCCAAAC[-/TA]TTAGTTTCCACACAA | 219333 |
rs771307303 | snp | A/G | 4.94401e-05 | 0.00497168 | missense, utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069291 | TTCCCTCTCAGTCCC[A/G]AGACTGATAGAAAAG | 219333 |
rs771307518 | snp | A/G | 1.77436e-05 | 0.0029785 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117772 | CAAGGACCTCGCACA[A/G]ACAATCATAGCGTGT | 219333 |
rs771310471 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27102460 | ACCCTCTCGTGGTTT[-/C]CCATGGCTTTCCAAA | 219333 |
rs771362492 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126465 | AGGCTTTGACTCTTT[A/C]TTTAGGGGTATTTTC | 219333 |
rs771378033 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158944 | AATTTTGGGGGGAGT[C/G]GGGGTGACACACACA | 219333 |
rs771420648 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27083468 | ATGCCAGCAGCCAGG[C/G]ACAGGAAAACAACAA | 219333 |
rs771433889 | in-del | -/AGTC | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124112 | AAATAATTTTTACAT[-/AGTC]AATCATGGAAAACAT | 219333 |
rs771434003 | snp | A/G | 2.09615e-05 | 0.00323733 | intron-variant | USP12 | GRCh38.p7 | 13:27095845 | TCTGAAAATAAAAAC[A/G]TTATATTAGAGAATT | 219333 |
rs771535642 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27072574 | TTAAAGAGATACCAA[A/C]AACTGCTTGCCCAAA | 219333 |
rs771563099 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27112985 | ATGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG | 219333 |
rs771618497 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27096693 | GATTCAAACTGGGCA[G/T]CCTGACTCCACCATG | 219333 |
rs771651005 | snp | C/T | 1.66388e-05 | 0.00288429 | missense | USP12 | GRCh38.p7 | 13:27095686 | TCTGGTGTGCTGTTA[C/T]TATTTTCATTATCAA | 219333 |
rs771684367 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142487 | ACCATCTTTATGAAA[C/G]AGAATGTCCCTGTTA | 219333 |
rs771701264 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27075013 | AATATATTTTAACAT[A/G]TAAAATTTTTAAGAA | 219333 |
rs771768990 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27094902 | CCTGTAATCCCAGAA[C/T]TTTGAGAGGCCAAGG | 219333 |
rs771772168 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141363 | GTCCACTAAAAGGAA[C/T]GTATGATTAAAAACC | 219333 |
rs771874624 | snp | A/G | 3.2963e-05 | 0.00405961 | intron-variant | USP12 | GRCh38.p7 | 13:27075183 | TATGTCCCCGGAGTT[A/G]CAATTACCTTCCACA | 219333 |
rs771886085 | snp | A/G | 1.73126e-05 | 0.00294211 | synonymous-codon, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27095820 | TTGTTGCATGTAGTT[A/G]TCAAAAAGCTCTGAA | 219333 |
rs771934295 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146416 | CAAAAAAAAGCACCT[A/G]TGTAATAACGCACAC | 219333 |
rs771945875 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153662 | ACACCCACTTTTCTG[A/G]TACTGTTCTGCTGGA | 219333 |
rs771968447 | snp | A/G | 2.42046e-05 | 0.00347875 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | USP12, USP12-AS2 | GRCh38.p7 | 13:27171604 | TACCATGGTACAGAT[A/G]GAGGCGAATTTGGAG | 219333 |
rs771991216 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137347 | AGCCATCTTCAATCC[A/G]CTTTATAAAAAGACT | 219333 |
rs771992778 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27094138 | TGATGAGGAGGGAGG[-/T]TATTTGTGTCTCCCC | 219333 |
rs772013428 | in-del | -/AA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161543 | TAATTTTATACCTTT[-/AA]AAAAAAATGTTACTA | 219333 |
rs772028828 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131517 | AGTGAGCAACGTGAT[C/G]GAAACTTGCCCCAGT | 219333 |
rs772047112 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27071224 | CTAAATTTTGTTTTA[A/T]AAAGAAACAGAAACA | 219333 |
rs772185400 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27075414 | TAAAAATGAAAACAA[A/G]ATTTCATAAAAGATA | 219333 |
rs772220921 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136505 | GCCCGCCTCAAATAA[A/G]CAAATACATACATAC | 219333 |
rs772225408 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27090357 | TGTATAAATAAAACA[C/G]CAAAGTACACTTTTG | 219333 |
rs772255113 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27114507 | TTCTCCTCTCTACTT[C/G]CAATAATATCAGGAA | 219333 |
rs772280146 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27170077 | GCGTATCTAAAAATA[A/G]TTAGCCCAAACAATT | 219333 |
rs772317280 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27089156 | ATGTGGGATTCTGGA[C/G]AGAATCCTTCTTCTA | 219333 |
rs772328534 | in-del | -/TCTC | 1.65751e-05 | 0.00287876 | frameshift-variant | USP12 | GRCh38.p7 | 13:27095742 | TTGTTTTTCCTGCTT[-/TCTC]TCTTCTTGTAAAATA | 219333 |
rs772334695 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160309 | AGAAGTAAAAGTTGC[C/T]TCCTTTTAGTTTTTC | 219333 |
rs772349160 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128180 | TGCCAAAAAAATAAA[C/T]GAACGAAAAACAAGC | 219333 |
rs772363934 | snp | C/T | 0.000137158 | 0.0082801 | intron-variant | USP12 | GRCh38.p7 | 13:27116483 | AAAACTGCTTCCGAA[C/T]ATGATTCTAAAAGCG | 219333 |
rs772370474 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157116 | TCTGAAATGTAAATA[A/C]TGACATTGGTGAAGT | 219333 |
rs772380947 | snp | C/T | 1.64901e-05 | 0.00287137 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069273 | AGTGTCTCTTCATCA[C/T]GGTTCCCTCTCAGTC | 219333 |
rs772389750 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148141 | TCAAAAAAAAAAAAG[-/A]CTTTTCTAAAACGAA | 219333 |
rs772400992 | snp | A/C | | | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27066015 | TGTTTTACACACATG[A/C]AATTCTGTTCTAGGG | 219333 |
rs772401049 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27081940 | ATTATGCTATAAACA[A/G]GTGTGCTGTCATCCA | 219333 |
rs772416327 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101961 | TTTCTATCTCATCCC[A/T]AGGACTGACAACCGT | 219333 |
rs772460970 | in-del | -/AAAC | | | intron-variant | USP12 | GRCh38.p7 | 13:27113269 | TCAAAACAAAAACAA[-/AAAC]AAACAAACAAACAAA | 219333 |
rs772488441 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27080657 | TTGGATCCCACAGAG[C/T]AGTGACAGAAATACA | 219333 |
rs772519834 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147784 | AAAATTTTAAAAAAC[C/T]GTCAACCAACAATGC | 219333 |
rs772568902 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162998 | GTTGTTTAGTTGGCT[C/T]TTAAACAAGGAGGCC | 219333 |
rs772608311 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149937 | GTGAAGCTCAGGCAG[C/T]AATGCTGCTCGCTGG | 219333 |
rs772616762 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27115357 | AGTGCTGATTCTTTG[C/T]TATAGGTTTTATGCA | 219333 |
rs772628688 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27085596 | TGAATTCATCCAAGT[A/G]AAGGTCAAAAATATT | 219333 |
rs772697082 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27115998 | ACAAGTTAGAAACTA[C/T]CTATCTCCAAGATTT | 219333 |
rs772717016 | in-del | -/AGA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167512 | AAACATTTATGTAAT[-/AGA]AGATTCCTTATTTTT | 219333 |
rs772731268 | snp | A/C | 1.80788e-05 | 0.0030065 | synonymous-codon, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27095826 | CATGTAGTTGTCAAA[A/C]AGCTCTGAAAATAAA | 219333 |
rs772749796 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150876 | AGAATGAAGTTACCT[C/T]TACCTCAAACCATGT | 219333 |
rs772764850 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152049 | AACAGCCATACACTG[C/T]TGGCAGGAACATAAA | 219333 |
rs772773383 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161480 | TCAGGGATCCCTGAA[A/G]AACCCAGGTAGACCA | 219333 |
rs772811002 | snp | G/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068409 | GTTCCTCCTGAAAAA[G/T]GATATTTATCTCCTC | 219333 |
rs772892997 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27103465 | TTTAGAAAAATGAAG[C/T]AAAACTTATGAGAAG | 219333 |
rs772899656 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27109299 | GCATTGCTCAAGTGA[A/G]CAACTGAATATTGTG | 219333 |
rs772970040 | snp | A/G | 0.000121051 | 0.00777886 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171552 | GCCCGCCCGCCCGAG[A/G]GGTCCCGGCAGCCCC | 219333 |
rs773000041 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27075729 | AAATGCACGGGGTGC[C/T]CAAGAGTGGTAGAGG | 219333 |
rs773107078 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156920 | GCATGATCCGGCGGC[A/G]AAAGCACTAGACTAA | 219333 |
rs773133014 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130124 | GGCACAGGACCACCT[C/T]CTAGAGCAGCTGCCT | 219333 |
rs773278504 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146447 | GGCTAAAGGCTAGGG[G/T]TATAAGGTAGGGAGA | 219333 |
rs773353272 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27096571 | TTTAGAGGCAGTATC[C/T]CATTTGATCCCCAAC | 219333 |
rs773355810 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27121305 | ACTGACTATGTGATC[C/T]TAAAAAAAAAAAAAA | 219333 |
rs773368253 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27081039 | TTTTTTTTGAGACGG[A/C]GTCTTGCTCTGTCGC | 219333 |
rs773406156 | snp | A/G | 3.42313e-05 | 0.00413697 | intron-variant | USP12 | GRCh38.p7 | 13:27116484 | AAACTGCTTCCGAAC[A/G]TGATTCTAAAAGCGT | 219333 |
rs773477867 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127189 | AATCTCATAGTTTTT[A/C]ACTATCCCATCAAAG | 219333 |
rs773484157 | in-del | -/TTTA | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118350 | ATACATGATACTGTC[-/TTTA]TTTTTTTGACTTGGG | 219333 |
rs773493753 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27085647 | CACCATAAATTAACA[C/G]GTTGATACTAGATCC | 219333 |
rs773530580 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145851 | AGAAAAGCAAAAAAA[-/A]TCTTGAGAGTACTAG | 219333 |
rs773561982 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27079130 | TATGAGACTACAACA[A/T]CCTCTCATTTTAGGT | 219333 |
rs773592927 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172609 | CTAAATATCTGCACA[C/T]TGAGCTGCAAAATAG | 219333 |
rs773595999 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132453 | GAAAAGAAAAAGAAA[A/T]AGCAAAGGAACAGAA | 219333 |
rs773609772 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170540 | ATATAAGCTCATGAG[C/G]AACTAATGAAACGAA | 219333 |
rs773639348 | snp | C/G | 1.66468e-05 | 0.00288498 | missense, upstream-variant-2KB, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116587 | TCTCTAATGCCGAAG[C/G]ATTGGCGCCCTATAA | 219333 |
rs773642216 | snp | G/T | 1.64833e-05 | 0.00287078 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069281 | TTCATCACGGTTCCC[G/T]CTCAGTCCCGAGACT | 219333 |
rs773655147 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145610 | AATCTGCTCATCACT[C/G]TGAAATATCATGATC | 219333 |
rs773706569 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139598 | TCCAGCCTGGGAGAA[A/C]GAGCAAGACTCCATC | 219333 |
rs773742823 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158262 | TGCCATGTGAAAAGA[C/T]TGGAATGATGCATCC | 219333 |
rs773818759 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153447 | ATAGAAATATTTTCT[A/G]GTTTCAAATAGGTTC | 219333 |
rs773828418 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27077364 | TGCACTATTAATAAA[C/T]GGCAGTCAGGTAAGA | 219333 |
rs773904858 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125134 | CATCTTTATTAGGAG[C/T]AAACAAAGTCTTCTG | 219333 |
rs773938163 | snp | A/C | 1.67562e-05 | 0.00289444 | intron-variant | USP12 | GRCh38.p7 | 13:27105704 | ACCTTCCTAGTATGT[A/C]ATTAATACAGTGGGA | 219333 |
rs773958151 | in-del | -/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156218 | CTCAACTCCTGCAAG[-/G]GAAAAAAAAAAAAAA | 219333 |
rs773978445 | snp | C/T | 1.65787e-05 | 0.00287907 | missense | USP12 | GRCh38.p7 | 13:27090158 | CATCTTTGCTGCTTA[C/T]CTGTAAAAACAGTGA | 219333 |
rs774092479 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163366 | AGTAACACATTATCT[A/G]TTTACATCTGGTATC | 219333 |
rs774106084 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147661 | AAAGAGGATGCATCA[C/T]TTATAAGGGAAACTC | 219333 |
rs774221432 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27080551 | CAGAAGTGGGGTCAG[C/G]CACACACGGAATAAA | 219333 |
rs774234173 | in-del | -/TTC | | | intron-variant | USP12 | GRCh38.p7 | 13:27082492 | TAAGGCTGTTTTGCT[-/TTC]TTATCATTTGTGGGT | 219333 |
rs774235578 | in-del | -/AGAAAAGAAAAAGG | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117092 | TGCTACCTAACACAA[-/AGAAAAGAAAAAGG]AGAAAAGAAAGAATG | 219333 |
rs774309150 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117621 | AAAACACCAACGTGT[A/G]TGTGTGTTTAATAGC | 219333 |
rs774413228 | snp | G/T | 3.54836e-05 | 0.00421195 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117782 | GCACAGACAATCATA[G/T]CGTGTCACAGTTTCA | 219333 |
rs774431474 | snp | G/T | 1.98375e-05 | 0.00314934 | intron-variant | USP12 | GRCh38.p7 | 13:27089846 | ATCAATTACAAAAAA[G/T]AAAATCACTTAAAAA | 219333 |
rs774475341 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131486 | TTTGGATTTTTCTAA[A/G]TAATCATTTTACCAA | 219333 |
rs774497100 | snp | C/T | 3.3012e-05 | 0.00406262 | missense, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105865 | CTAGGTTGACTCTTA[C/T]ACGCAAGAACTTTTT | 219333 |
rs774512744 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27121441 | ATTCAATCCACCCAC[A/G]AAGAATTCCTACAAA | 219333 |
rs774575167 | snp | A/G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101915 | CATGAAACGCTGCTT[A/G/T]TCCATGCAGGTTCCT | 219333 |
rs774596624 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27107280 | CAGTGAGCCAAGATC[A/G]CACCACTGCACTCCG | 219333 |
rs774600825 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27073975 | ACTCCTTTAAGATGT[A/G]ATCACTCTTAATTTA | 219333 |
rs774617376 | in-del | -/AT | | | intron-variant | USP12 | GRCh38.p7 | 13:27083860 | CCTTTTTGGGAGAAT[-/AT]ATATATATATATATT | 219333 |
rs774752036 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158956 | AGTGGGGGTGACACA[A/C]ACACAATACCTCATG | 219333 |
rs774782279 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133220 | TCAATAAACTTAACG[C/T]AAACACCACACTCAC | 219333 |
rs774821896 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173120 | TGCAGATTGAATATA[A/G]CCAAGCCCCATGGTA | 219333 |
rs774847034 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27112006 | GGTATCCAATTTGTA[A/G]TCTTATCTACCAAAT | 219333 |
rs774866342 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146704 | GTTTCAGAAGGCACT[C/T]AAGATGGCAATATTC | 219333 |
rs774917118 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27073155 | GAAGACTTCCAGAGC[A/G]GAGGGGCAGGAAGGC | 219333 |
rs775000893 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27070645 | CACAACCTCCGCCTC[C/G]CGGGTTCAAGCGCTT | 219333 |
rs775059115 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126772 | CAAAGTTTAAATTTA[C/G]AACAAATATTTGTTC | 219333 |
rs775061444 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27094950 | CCCAGGAGTTCAAGA[C/T]CAGCCTGAGCAACAC | 219333 |
rs775084333 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173306 | ACCTCTAGGGCCTAC[C/T]TGGGCCTTGTCCGAG | 219333 |
rs775115107 | snp | A/G | 2.56941e-05 | 0.00358418 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171643 | TAGGATTTCCATCCG[A/G]CCAGCGCCATCTTCC | 219333 |
rs775161471 | snp | A/G | 1.65143e-05 | 0.00287348 | synonymous-codon | USP12 | GRCh38.p7 | 13:27090117 | TGTATTTTGTTCCAC[A/G]TCAACAGAAAGGTCT | 219333 |
rs775166081 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163927 | TCCTCAGCACAACTA[A/T]AACCCACTCAAGACA | 219333 |
rs775176983 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27079408 | TGACTGGTCAAAGAC[C/T]TGGAATTTGAACCAA | 219333 |
rs775255255 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27109277 | CCTAAACACCCCAGC[A/G]ATTTCAGCATTGCTC | 219333 |
rs775275966 | snp | A/G | 1.65477e-05 | 0.00287638 | synonymous-codon | USP12 | GRCh38.p7 | 13:27089939 | ATACTTGTATTCACT[A/G]CACAGAGTTTCTGTG | 219333 |
rs775342367 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142735 | ACATCACCAAAAAGA[A/T]TGACTGTAATTTATT | 219333 |
rs775346823 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139728 | TCATGTACAAATAAA[C/T]GCAGGTGAAGTCACA | 219333 |
rs775415838 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133005 | ACTGTTGATTCCAAA[C/T]TCAAGCTTCCACCAG | 219333 |
rs775436781 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153713 | CCCCAAAAAGACGTA[C/T]CTTCCTTAAAAGTAA | 219333 |
rs775447769 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27106007 | TCAAGAGAGAAATTC[A/C]CGGTATATGGTTGAG | 219333 |
rs775462333 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27074110 | TTGTCCTTAAAAATT[A/C]TCATCAGAGGCCGGG | 219333 |
rs775511468 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167418 | GACAAATTCAAAAGA[C/T]GAGTGGGCTTAAATA | 219333 |
rs775615463 | snp | A/C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168899 | ACACTTCAGTACTTA[A/C/T]AGAATAAAATTTCAA | 219333 |
rs775637485 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27110481 | GCCCCACTGAAACAG[A/G]AGTTACCAACTTTTT | 219333 |
rs775650252 | snp | C/T | 1.65135e-05 | 0.00287341 | missense, intron-variant | USP12 | GRCh38.p7 | 13:27071108 | AACAACCAAAAATCA[C/T]GACTCTTAACTATTG | 219333 |
rs775695910 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27100348 | CCAACCCTTTCTAAG[C/T]TGCTCATTCTAGGTC | 219333 |
rs775726945 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27109371 | TTAAGCAAAATCACT[A/G]AACTTTAATCAAGTC | 219333 |
rs775739100 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27090515 | CTGAATAAAAATGCT[G/T]CACACAGGACAGGAT | 219333 |
rs775780539 | snp | G/T | 1.64868e-05 | 0.00287109 | missense, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105829 | AGATCTGCTAAGCAT[G/T]TAAGAAGGCTCTCCT | 219333 |
rs775794002 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143983 | CCAAGTTGGAAGGAT[C/T]ACTTGAGGTCAGGAG | 219333 |
rs775797529 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136519 | AACAAATACATACAT[A/T]CATACATACCCTTTA | 219333 |
rs775813282 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157127 | AATACTGACATTGGT[A/G]AAGTTTCTTCACAGC | 219333 |
rs775851788 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066190 | ATAGATATTATTTTG[C/T]ATTTATATAGTGCCT | 219333 |
rs775885587 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150182 | ACATTGTATACCTGT[A/G]TCAAAATATCACACT | 219333 |
rs775893701 | in-del | -/T | 1.648e-05 | 0.0028705 | frameshift-variant, utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069358 | TGTCAACCCGTAGAA[-/T]TCTTCAATAGCTTGT | 219333 |
rs775934182 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27114519 | CTTCCAATAATATCA[C/G]GAATAGCATTGTATC | 219333 |
rs775965662 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161499 | CCAGGTAGACCAATA[C/T]TGTAGAAATAAAGGC | 219333 |
rs776006811 | in-del | -/AAAAAAAAA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163769 | AGCAAGACCTGTCTT[-/AAAAAAAAA]AAAAAAAAGAAAAAA | 219333 |
rs776008548 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27100718 | CCACTAAGGCAAGGA[C/G]TGGAAGATAATTATG | 219333 |
rs776011824 | in-del | -/AATT | 2.31581e-05 | 0.00340272 | intron-variant | USP12 | GRCh38.p7 | 13:27095857 | AACATTATATTAGAG[-/AATT]ATTTCAGAATTCATA | 219333 |
rs776036661 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143025 | TTGAACTGGGGAGGC[A/G]GAGGTTGCAGTGAGC | 219333 |
rs776055553 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160371 | AACCAGTCACATGAC[A/G]ATGGCAGGTCCTTGT | 219333 |
rs776085168 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135231 | GAGGTTGCAGTGAGC[C/T]GAGACCACAAAACCT | 219333 |
rs776118708 | snp | A/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067897 | CCAAAAAAACTGCAA[A/T]CGTTTACATATATTT | 219333 |
rs776203225 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101974 | CCTAGGACTGACAAC[C/T]GTGCCTGCCACATAA | 219333 |
rs776208958 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27082139 | TCTCTAGCTATGACA[A/G]TCCTAAACACCCTCT | 219333 |
rs776214314 | snp | C/T | 1.64822e-05 | 0.00287068 | synonymous-codon, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105777 | CTTAGGGGGTATTAC[C/T]CCAACCTTTTTCTTC | 219333 |
rs776276516 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27120199 | ACATAATGGTCACAT[A/T]ATCACCCAAAAATTT | 219333 |
rs776290820 | snp | A/G | 2.46984e-05 | 0.00351405 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | USP12, USP12-AS2 | GRCh38.p7 | 13:27171631 | GGAGACTGTCATTAG[A/G]ATTTCCATCCGGCCA | 219333 |
rs776304660 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27114633 | AGAGCCATTATCTGT[A/G]ACAATATTCTTCTGA | 219333 |
rs776318514 | in-del | -/AGAC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144707 | AAAAACAAAACAGAA[-/AGAC]CACAGAAAACTTTTT | 219333 |
rs776354230 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27073609 | AATTCTAAAAATCTA[C/G]CATGATTTAAGTAGA | 219333 |
rs776407119 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066445 | AAAGTGTTTTTAAAG[A/G]AAGTATCAAGAGTAG | 219333 |
rs776407330 | snp | A/G | 0.000207684 | 0.0101882 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171559 | CGCCCGAGAGGTCCC[A/G]GCAGCCCCGGCCGCC | 219333 |
rs776417947 | snp | C/T | 1.64846e-05 | 0.0028709 | missense | USP12 | GRCh38.p7 | 13:27075269 | GAAGTGTTAAACAGA[C/T]GAAGTTCTAAAGGAA | 219333 |
rs776442770 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27072808 | TTCTAGGCTGGGCAC[C/T]GGGGACAGAGAAGGA | 219333 |
rs776455557 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141785 | CATCCCTAATTTGAA[A/C]ATCTGAACTCCAAAA | 219333 |
rs776464235 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27113925 | GAAAGTTTCATTTTT[A/G]TTTATTTCTATAATG | 219333 |
rs776483418 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164177 | CAAAGGCAACAGTAC[G/T]CTAACTCTACTGAAA | 219333 |
rs776486367 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127362 | ACCAATGACATAAAA[C/G]GGAACAGAGAGGTTC | 219333 |
rs776503316 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27099117 | CTTCCTATTTGGACA[C/T]ATATATTTAAGTGCA | 219333 |
rs776522467 | snp | C/T | 1.77423e-05 | 0.00297839 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117774 | AGGACCTCGCACAGA[C/T]AATCATAGCGTGTCA | 219333 |
rs776565796 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142595 | CAATCACTGGATTTG[C/G]GTAAAAGGTATTTGG | 219333 |
rs776574560 | in-del | -/ATAC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136509 | GCCTCAAATAAACAA[-/ATAC]ATACATACATACATA | 219333 |
rs776580452 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27106111 | CAACTCTCAAAAATT[A/C]TTTGGAAATCACAAA | 219333 |
rs776618560 | in-del | -/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140295 | TTAATATTGGAGCTA[-/G]GTTGCATAGTACACG | 219333 |
rs776627654 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166624 | GTAAGCAAAGCCATA[A/T]GATATAAAATAAGAC | 219333 |
rs776661203 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148065 | GCCCAAGAGGTTGAG[A/G]CTGCAGTGAGCTGTG | 219333 |
rs776662456 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27095091 | GCCCAGGAAGTCGAG[A/G]CTACAGTGAGCTGAG | 219333 |
rs776749899 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27107240 | TGAGGTATGAGAATC[A/G]CTTGAACCTGGGAGG | 219333 |
rs776764566 | in-del | -/AA | | | intron-variant | USP12 | GRCh38.p7 | 13:27120622 | AGCAAAACTCCATCT[-/AA]AAAAAAAAAAAAAAG | 219333 |
rs776809891 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27098980 | GGCTCATGTCTGTAA[A/T]CCCAGCACTTTGTGA | 219333 |
rs776824928 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27123091 | AGTGAGAGTCCATCT[-/C]AAAAAAAAAAAAAAA | 219333 |
rs776857971 | in-del | -/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156218 | CCTCAACTCCTGCAA[-/G]GAAAAAAAAAAAAAA | 219333 |
rs776868769 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27081850 | CACATGTATTGTCAA[-/T]AAGCAGTAATATTTT | 219333 |
rs776893310 | in-del | -/A | 0.0240487 | 0.106986 | intron-variant | USP12 | GRCh38.p7 | 13:27105953 | CCCAAACTGCAACAG[-/A]AAAAAAAAAAGTTTT | 219333 |
rs776934879 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145235 | GAATGACAGGTGGCC[A/G]AAAACATGAAATTCT | 219333 |
rs776951433 | in-del | -/AAAG | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157328 | TGGACCTAAGATCAC[-/AAAG]AGGTGTATATAATCC | 219333 |
rs776979388 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27111528 | GGTCTTATCATTGAT[A/T]TTTTGATTGCTTAGT | 219333 |
rs777002607 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155478 | TAATGCACACACAAA[C/T]TGGTCCATTTTAAAT | 219333 |
rs777034089 | snp | A/G | 1.65261e-05 | 0.0028745 | synonymous-codon, intron-variant | USP12 | GRCh38.p7 | 13:27071083 | TACTTCTACAATGTC[A/G]TCATCAAACAACAAC | 219333 |
rs777057315 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27103162 | CATAGTATGGCAGGA[A/C]ATTAATTTAGTAAGA | 219333 |
rs777068781 | snp | A/G | 2.17782e-05 | 0.00329979 | intron-variant | USP12 | GRCh38.p7 | 13:27095848 | GAAAATAAAAACATT[A/G]TATTAGAGAATTATT | 219333 |
rs777069258 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27091093 | AAGATACAGCAACAC[C/T]ACAAGATAACTGACC | 219333 |
rs777101012 | in-del | -/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164586 | AGCAAAGACTTACTA[-/G]GTTTTTCTTCCTAAA | 219333 |
rs777127389 | snp | A/G | | | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169137 | TCCTTCCCCTTCAAG[A/G]CCCTCACAATTGAGT | 219333 |
rs777176886 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27098604 | CTCAACTGTTGCTGC[G/T]GGGAGTATAAACTGG | 219333 |
rs777212397 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27091164 | GACAACTCAGAGAGA[-/A]AAAAAGAGGACATGA | 219333 |
rs777229958 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165724 | ATTAGCAAATAGCTT[A/T]GTGAATTATTAGGCT | 219333 |
rs777231624 | in-del | -/GGGCGGGGGAGGA | 3.5121e-05 | 0.00419038 | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171681 | CACAGCGGCGGCGGC[-/GGGCGGGGGAGGA]GGGGAGCCGGGCCGC | 219333 |
rs777256034 | in-del | -/AT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161551 | TACCTTTAAAAAAAA[-/AT]GTTACTAATAGGGAA | 219333 |
rs777259177 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27075569 | ACAACATTCTGAACA[A/T]CTTAATATGACCCCA | 219333 |
rs777275889 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27100021 | TCTCCCTGCTCAGAG[C/T]AGAAGTCTATGCAAC | 219333 |
rs777321494 | in-del | -/CT | 1.65726e-05 | 0.00287855 | splice-acceptor-variant | USP12 | GRCh38.p7 | 13:27089967 | GTGTTGCTGAAACCC[-/CT]GTGTGAAATTCAAAA | 219333 |
rs777334260 | snp | C/T | 1.64904e-05 | 0.00287139 | synonymous-codon, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105747 | ATTTTCTTTCCGTAA[C/T]CTTGTGATGAACTTC | 219333 |
rs777450034 | snp | C/T | | | synonymous-codon | USP12 | GRCh38.p7 | 13:27075274 | GTTAAACAGACGAAG[C/T]TCTAAAGGAAAAACT | 219333 |
rs777464957 | snp | C/T | 1.8936e-05 | 0.00307695 | splice-acceptor-variant, intron-variant | USP12 | GRCh38.p7 | 13:27105945 | GCAGGTATTCCCAAA[C/T]TGCAACAGAAAAAAA | 219333 |
rs777509893 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164343 | AATTTTTATTGGTAC[A/G]TAGCTTTGGACATGT | 219333 |
rs777546267 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27111283 | TAATATTAACTTTCA[C/T]TCAAGGTCCTAAGAC | 219333 |
rs777622476 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27169813 | AGAAAACAGGGGCTG[C/T]CCTGACCAATACTGC | 219333 |
rs777645187 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27091039 | GCTAACCATAGGACC[A/G]AAACCCCTTCTGTAA | 219333 |
rs777646259 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27081565 | CAAACTGTTTTTAAT[A/G]TTAATATTTTAACCT | 219333 |
rs777649503 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27101327 | GACAATCCCTGTGAA[A/C]TGTATTATATTTAAT | 219333 |
rs777724173 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142024 | CCACTTGCAAGGCTG[A/C]AGCAGGAGAATTGCT | 219333 |
rs777746936 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27097615 | TGGTTCTACTTCTAA[A/C]TGCACGCGTGGCATA | 219333 |
rs777766728 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27110106 | CAAAATGCCATGATG[A/C]CTAGGATTTCCTTTT | 219333 |
rs777784499 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158494 | ATGGTGCGTATGTCA[C/T]AGAGTGTACTCACGC | 219333 |
rs777795399 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160009 | CCTGAAAGAGCGGAA[C/T]TGCGAACACTTGGCA | 219333 |
rs777840514 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101748 | ACAAAATACCATTTA[C/T]GCTCTTTTGGAGAAA | 219333 |
rs777843041 | snp | C/T | | | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27065881 | TTTACCTATTTTACC[C/T]TCTAAGATTCTATGA | 219333 |
rs777921413 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27104508 | GGTTATATTTGATTT[C/T]CTAAAAAAACAAGAT | 219333 |
rs777930013 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27080336 | TACCATTACTGGAAC[G/T]GGCTACAGGGGAATA | 219333 |
rs777992196 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154632 | TTTCACCTCTAATAC[A/G]TTTTTTAAAGTTAAA | 219333 |
rs778000643 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27119638 | CACTCAACATTCTAT[C/T]GTTTCCGATCACTTT | 219333 |
rs778026583 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152221 | ATACCCATAAGGTAG[-/C]AAATGGCCCAAATGT | 219333 |
rs778029402 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27085511 | GGTTTTTTACTAAGA[A/G]CTATGGTCTGTATAC | 219333 |
rs778119272 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27105583 | TTCACTAAACGAGTG[A/C]CTCTTTGAAGAAAGG | 219333 |
rs778128428 | in-del | -/TTT | | | intron-variant | USP12 | GRCh38.p7 | 13:27096144 | TTACCTGACTTATTA[-/TTT]CACAAATATTTCAAC | 219333 |
rs778231883 | in-del | -/TTTC | | | intron-variant | USP12 | GRCh38.p7 | 13:27085165 | ATGTTTTCTTTTTTC[-/TTTC]TTTCTTTCTTTCTTT | 219333 |
rs778292350 | snp | C/T | 0.000141937 | 0.00842309 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117766 | AAGAAACAAGGACCT[C/T]GCACAGACAATCATA | 219333 |
rs778303699 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27118855 | AATCACATGCCACTC[A/G]CCTTGTATTCTAACC | 219333 |
rs778305549 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27086687 | GGTGGCTTTTGCTCA[C/T]AGATGGGCCTTCCTC | 219333 |
rs778313488 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27106769 | TTATAGGAGAAGAGG[A/G]AAAATAATGGAGAGA | 219333 |
rs778380247 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142275 | GGAACGGTATACCAA[A/T]CAATTGACTTGTACT | 219333 |
rs778382543 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126130 | AGTGGTTCTCCCAGC[A/C]TGGTGTTTCGAGCTC | 219333 |
rs778390019 | snp | C/T | 2.34651e-05 | 0.0034252 | intron-variant | USP12 | GRCh38.p7 | 13:27071197 | TATTTATTAATATTA[C/T]TCTTTCATGCTCTAA | 219333 |
rs778392282 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155811 | AATTAAGTCTAGATG[C/T]GGAAAAGGTTCAACT | 219333 |
rs778394340 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27074216 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 219333 |
rs778408366 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138613 | TTTTGACTTTGCTGC[A/G]GGAAAGCCTTGGTAT | 219333 |
rs778454738 | in-del | -/TA | 3.4064e-05 | 0.00412684 | intron-variant | USP12 | GRCh38.p7 | 13:27095575 | AATTCAATTTTTCTC[-/TA]TACAAAATTGTATGA | 219333 |
rs778472450 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140817 | AGATTAGAGTTGACA[A/G]TTATGTCCAAGTCAG | 219333 |
rs778545047 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170897 | CGTGCCTCTCAGAGG[-/A]GAAAATGGAGAGAAT | 219333 |
rs778558583 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167172 | GAGGCTGAGGCAGGG[G/T]AATCACTTGAACCTG | 219333 |
rs778584560 | snp | C/G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134235 | CTCTCTATAGGGTTA[C/G/T]TAACAACTTATAGGA | 219333 |
rs778592729 | in-del | -/CA | | | intron-variant | USP12 | GRCh38.p7 | 13:27123091 | AGTGAGAGTCCATCT[-/CA]AAAAAAAAAAAAAAT | 219333 |
rs778602805 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27106967 | AGGTGACTTAAAGAA[G/T]GTTTACCATACATGC | 219333 |
rs778604159 | in-del | -/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161440 | TACTTGTGCCCAGAT[-/G]GGCTCTAATTTTGAA | 219333 |
rs778627216 | in-del | -/AAAAAAAATT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161899 | AAATAAAAAAAAATA[-/AAAAAAAATT]AAAAAAAATTAAAAA | 219333 |
rs778681258 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27111324 | TCTTTCAAGAGTAGA[C/G]CCTTCATGCAAAAGG | 219333 |
rs778684013 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27100106 | CATCCCTCCGAGGCC[A/G]GGCCAAGTCATGCAT | 219333 |
rs778691180 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27073222 | ACCCTGGGGTGGGGG[C/T]GGGATACCAAAGACC | 219333 |
rs778748353 | in-del | -/A | | | | | GRCh38.p7 | 13:27118344 | TTCTATATACATGAT[-/A]CTGTCTTTATTTTTT | 219333 |
rs778815459 | snp | C/T | 6.60317e-05 | 0.00574556 | synonymous-codon, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105738 | AGAATTACCATTTTC[C/T]TTCCGTAATCTTGTG | 219333 |
rs778853659 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162540 | AATGGATCTTCAAGA[G/T]GACAGATAGAGAAAG | 219333 |
rs778864821 | snp | G/T | 1.69481e-05 | 0.00291098 | missense | USP12 | GRCh38.p7 | 13:27095809 | TCATGGGCATCTTGT[G/T]GCATGTAGTTGTCAA | 219333 |
rs778876958 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27078497 | ATGTTGTATTCTAAC[A/G]TAACAGGGGGTTGCC | 219333 |
rs778879280 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27112713 | GATGATGCCATCAAC[A/C]CTTTGACATCATGGA | 219333 |
rs778879962 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27112990 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCA | 219333 |
rs778926543 | snp | A/G | 1.75194e-05 | 0.00295963 | intron-variant | USP12 | GRCh38.p7 | 13:27090036 | TAAAAAATATTCCAG[A/G]CTAAAAATAATTATT | 219333 |
rs778954794 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147170 | AAGACCCTAGGAAAC[G/T]AATACACCATGGTAT | 219333 |
rs779044608 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146335 | TGAACCCGTGAGGCA[A/G]AGGTTGCAGTGAGCC | 219333 |
rs779048917 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27082735 | TAATTGGCCTAATTT[A/C]AATATTGTTGTGTCT | 219333 |
rs779065358 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137168 | TACAAAATATATTCC[C/T]TCAATTCCTTCATTT | 219333 |
rs779095414 | snp | C/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067328 | ACAATTTGGTTTAAG[C/G]CTTCAAAATAAAAAG | 219333 |
rs779101032 | snp | A/G | 1.65622e-05 | 0.00287764 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116578 | CAATCTCTTTCTCTA[A/G]TGCCGAAGCATTGGC | 219333 |
rs779108487 | in-del | -/TG | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127583 | AGTAGTGTTTATGTT[-/TG]TGTATACATCCCATT | 219333 |
rs779134678 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27115247 | ATTCTAACTGAAATG[C/G]TGTTTTTTAAATTAG | 219333 |
rs779151724 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136400 | CTACTCAGGAGGCTG[A/C]AGCAGGAGAATCGCT | 219333 |
rs779174994 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27108888 | AGAGGTTGCAGTGAG[C/T]CAAGATGGTACCACT | 219333 |
rs779190760 | snp | C/T | | | synonymous-codon | USP12 | GRCh38.p7 | 13:27095667 | CTCATGAACCCACGT[C/T]GGGTCTGGTGTGCTG | 219333 |
rs779242803 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27104290 | CCTACCTTGGCCTCC[C/G]AAAGTGCTGGGATTA | 219333 |
rs779294321 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27074842 | TTACAACCATTGATA[C/T]GCTGAACATACGCAA | 219333 |
rs779332475 | snp | A/T | 6.61857e-05 | 0.00575226 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069245 | AAATAACCAGAGAAG[A/T]AATGAGGCAGAAAGT | 219333 |
rs779332956 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27102797 | CTTCCCCACGAGGGT[C/G]TCAGGTACCTGAAGG | 219333 |
rs779384835 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27081809 | ATTAATCTCTTTGTG[C/T]GTCTCCATCAGAGCT | 219333 |
rs779389599 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129739 | ATAATTTTTGTGAAG[A/G]ATGTTAGAGAAATGC | 219333 |
rs779416252 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161291 | TTTTTGGACTAAGAT[A/T]ATCACATACAAAGCA | 219333 |
rs779430590 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129644 | CCAGGAGTTCGAGGC[C/T]GCAGTGAACTATGAC | 219333 |
rs779509583 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27114334 | TAACCAGCTACAATA[G/T]AAAAGGAAAAAAGGC | 219333 |
rs779516472 | snp | A/C | 1.77448e-05 | 0.00297861 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117745 | AAAGGAGAAAAAACA[A/C]AATTCAAGAAACAAG | 219333 |
rs779535682 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156080 | CATGAGGTAAAAAGC[A/T]GCCAGCAGCTCCGTA | 219333 |
rs779553931 | snp | A/G | 1.65312e-05 | 0.00287495 | synonymous-codon, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116528 | TACATTGACTAATCC[A/G]AAATAGTGCTCATTG | 219333 |
rs779614215 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168453 | GGATTAGCCACCTCA[A/G]CTGCAAAACACAGCC | 219333 |
rs779633432 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27074777 | CACACAGGTAAAATC[-/A]AAAAAATGAATCTTT | 219333 |
rs779642041 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143251 | TAAATAAAAATCTAT[C/G]ATGACACAAAAAAGA | 219333 |
rs779650497 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076357 | TTATGCCTTTAAATG[C/T]CATTTCTCCCTGAGA | 219333 |
rs779734407 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156727 | TCAGGAGGCTAAGGC[A/C]GGAAGAATTGCTTGA | 219333 |
rs779742764 | snp | A/G | 1.64844e-05 | 0.00287087 | missense | USP12 | GRCh38.p7 | 13:27075270 | AAGTGTTAAACAGAC[A/G]AAGTTCTAAAGGAAA | 219333 |
rs779799318 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167401 | GTCCAAAATGTATTT[C/T]AGACAAATTCAAAAG | 219333 |
rs779802063 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27097181 | AAAAAAAAAAAAAAA[-/T]GCAGGCCAAGCGCAG | 219333 |
rs779807726 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135699 | CAGCCTGGGTGACAG[A/T]GTGAGACTCTGTCTC | 219333 |
rs779831162 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27109770 | AATACAAAAACTAGC[C/T]GGGCGTTTTACTCCT | 219333 |
rs779888952 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147326 | ATTTTATTTTAGTTT[A/G]TTTCCAATTTAGTTA | 219333 |
rs779897534 | snp | C/T | 1.65759e-05 | 0.00287883 | missense | USP12 | GRCh38.p7 | 13:27095749 | TCCTGCTTTCTCTCT[C/T]CTTGTAAAATATCAG | 219333 |
rs780003702 | snp | C/T | 6.42983e-05 | 0.00566966 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171548 | CGCCGCCCGCCCGCC[C/T]GAGAGGTCCCGGCAG | 219333 |
rs780024763 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27101211 | CTTAGAGTATACTGA[A/C]TATGCCAGAATTTTG | 219333 |
rs780080497 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158047 | AACTGTGTTCCCTAA[A/T]AAAGGTACGTTTAAG | 219333 |
rs780106302 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155143 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCATT | 219333 |
rs780127237 | snp | C/T | 3.3428e-05 | 0.00408814 | intron-variant | USP12 | GRCh38.p7 | 13:27090014 | GATACCAGGAAATCA[C/T]GTATCTTAAAAAATA | 219333 |
rs780131358 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27077117 | GAGTGTTGTACAACT[C/T]AAATAAAACAATGCT | 219333 |
rs780143057 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27092705 | CTTTCTAATACCTTA[C/T]ACAGAAATTAACTCA | 219333 |
rs780143819 | in-del | -/AAA | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173688 | TCTCTACTAAAATAC[-/AAA]AATTAGCCAGGCGTA | 219333 |
rs780143969 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27170097 | CCCAAACAATTCTCC[A/T]AAATCATTTTAATAT | 219333 |
rs780184468 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139119 | TCCCAGATTTATGAT[A/T]TCTTTGGGAAACCAG | 219333 |
rs780203482 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124704 | AGCAGCCCATGTGAC[C/G]GTGTGAAGGTATAAA | 219333 |
rs780221632 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27091197 | TGTTTAAGGAAAACA[C/T]ATCAATTTTGTAGAA | 219333 |
rs780227869 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27083223 | GATCATGTATCACCG[C/T]AACAATATAATAATG | 219333 |
rs780297894 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129760 | AGAGAAATGCTGCAA[A/G]GAACTTTATTCCATT | 219333 |
rs780309927 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27104555 | TAATAAAGTACATAC[A/G]TTTAGCTTTCATTAG | 219333 |
rs780314592 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27097394 | CGCTTGAACCCGGGA[A/G]GTAGAGGTTGCAGTG | 219333 |
rs780321830 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161552 | ACCTTTAAAAAAAAA[C/T]GTTACTAATAGGGAA | 219333 |
rs780364141 | snp | A/G | 0.000110187 | 0.00742167 | intron-variant | USP12 | GRCh38.p7 | 13:27075423 | AAACAAAATTTCATA[A/G]AAGATATCCACCATG | 219333 |
rs780393879 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27092209 | AACTCCAATGAAAGA[C/T]AGCAAAAAAAGTGGT | 219333 |
rs780486629 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27081978 | TTTCTTTTCTACAGC[A/C]CAGGCAGGGTAGATT | 219333 |
rs780538190 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069012 | GCGTGCCAATGACTG[A/G]AAGGCTGTTTTAAAA | 219333 |
rs780555699 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143615 | GAAATATTTCCCTTA[G/T]GATGAAGACATTGGT | 219333 |
rs780571214 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145840 | TACAAAATGGAAGAA[A/G]AGCAAAAAAAATCTT | 219333 |
rs780578870 | snp | A/T | 3.60887e-05 | 0.00424771 | intron-variant | USP12 | GRCh38.p7 | 13:27105977 | AAGTTTTGTTAAATT[A/T]AGGGCAACACATTTT | 219333 |
rs780581105 | in-del | -/AC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140386 | AGCACAGTTATGAAA[-/AC]ACACAGTCAAAACTT | 219333 |
rs780586929 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116721 | AGCTGCCCTACACAG[A/G]TGCGTCTTTATCCTT | 219333 |
rs780605557 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130964 | GTCAGAAAAATTCTG[A/G]ATGAAAAGATCAGTT | 219333 |
rs780640218 | snp | A/G | 0.000185117 | 0.00961894 | intron-variant | USP12 | GRCh38.p7 | 13:27105954 | CCCAAACTGCAACAG[A/G]AAAAAAAAAGTTTTG | 219333 |
rs780642794 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163615 | ATCTTCTCATCAGGA[C/T]ACACAGAGAAAATAG | 219333 |
rs780644372 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27076641 | TGCCTGACATATGAT[A/G]GATGCCAAATGCTGC | 219333 |
rs780728504 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076535 | ACATGGTAACAATTT[C/T]AGGTGATTATGGTTC | 219333 |
rs780728980 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162683 | CTTTCATTTTAGGTA[A/G]GTTTCTTATTGAGCA | 219333 |
rs780746271 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157719 | ACCTTTGTCCTCTTC[A/G]TTTTTCTCCAAGTTA | 219333 |
rs780772495 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147355 | TACGAATGTCTTCTA[C/T]GAGAATGCTTGTAAT | 219333 |
rs780773716 | snp | C/T | | | missense, upstream-variant-2KB, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116571 | TCTGGACCAATCTCT[C/T]TCTCTAATGCCGAAG | 219333 |
rs780783344 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131146 | CAAATTCAGAATGCA[A/G]GAAGCAGTCAATATG | 219333 |
rs780842426 | snp | A/G | | | intron-variant, splice-donor-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162924 | TCACTCCCTGTGTGG[A/G]TGTGTATTTATCCTT | 219333 |
rs780871484 | snp | A/G | 1.65949e-05 | 0.00288048 | synonymous-codon, utr-variant-5-prime | USP12 | GRCh38.p7 | 13:27116516 | TCAATGGATACTTAC[A/G]TTGACTAATCCAAAA | 219333 |
rs780940079 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27122361 | AAGTGCCTTTCACCT[A/C]CTCCCATGATTCTGA | 219333 |
rs781031644 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137064 | AAATAAGTGACAAAG[A/T]TATTGAACAAAGATA | 219333 |
rs781075154 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27102738 | CCCAGTCTTCTTTTT[C/T]TCGTGACAGTGACAC | 219333 |
rs781082625 | in-del | -/TTCCTC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156383 | ATTTCCTCAAAAGAT[-/TTCCTC]AAACTATAATAAAAA | 219333 |
rs781104331 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27074779 | ACACAGGTAAAATCA[A/G]AAAATGAATCTTTGA | 219333 |
rs781135565 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155230 | GGGACTACAGGCGCG[C/T]GCCACCATGCCCGGC | 219333 |
rs781140620 | in-del | -/T | 1.98356e-05 | 0.00314919 | intron-variant | USP12 | GRCh38.p7 | 13:27089846 | ATCAATTACAAAAAA[-/T]AAAATCACTTAAAAA | 219333 |
rs781171757 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27101098 | CAAAAATACCTCCAA[G/T]GACTTGAATGCTCTG | 219333 |
rs781213796 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27169639 | TGGATGGAAGCCCTA[G/T]AAAGAGCTTCTGATT | 219333 |
rs781222593 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27112859 | TGCTAATATTTTCTT[C/T]CTATTCCCAATGGAT | 219333 |
rs781228240 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27109021 | CCTCTTTAGTCTCCA[C/T]TGACAATTGCAAACT | 219333 |
rs781243696 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172372 | AGTTAAGATAACCCG[C/G]GTATGCGTCCCAAGC | 219333 |
rs781286317 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27072224 | CTTGTGTGTTATGGG[A/G]AGAGGGTCAGAAATG | 219333 |
rs781305117 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168512 | GTTATTTCACACTTA[C/T]TAAGTATAATATTAA | 219333 |
rs781366483 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27078847 | TGAACACCCTAACTA[C/T]GGACTTAATTGACAT | 219333 |
rs781368894 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27092355 | GTTATTTTGTGGATA[C/T]CGACGAACTTGATTC | 219333 |
rs781404171 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173818 | TTGCACCCCAGCCTG[A/G]GTGACAGAGTGAGAC | 219333 |
rs781416584 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158627 | GGTAACTGTAACACA[A/G]TGGTAAGTATTCATG | 219333 |
rs781430787 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141754 | AATGACAGTCCTACT[A/G]CTAGTAGAGGTTGAG | 219333 |
rs781433380 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27084876 | CTATTTAGGGTCTTC[C/T]GTGATTCCATGTGGA | 219333 |
rs781454967 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27082788 | GAGAGGTAGGAGGGG[A/G]AAAACGTCAGGTGGG | 219333 |
rs781476063 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139792 | TCACATATTTATTTT[-/A]AAAACATTTTCTTAT | 219333 |
rs781521247 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069027 | GAAGGCTGTTTTAAA[A/G]GAGGAGCTGGTATCT | 219333 |
rs781549579 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132502 | AAATTACTGCCCCTC[A/G]AAGGAGACTCTTCCA | 219333 |
rs781550624 | snp | C/T | 6.60982e-05 | 0.00574846 | intron-variant | USP12 | GRCh38.p7 | 13:27075143 | TTGAATGTACCCTGC[C/T]CTTCTAACCTAGGAA | 219333 |
rs781560839 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27080286 | CAAAGCAAATCCCTA[G/T]TGCTGATATGATTTT | 219333 |
rs781633488 | snp | C/G | 1.88966e-05 | 0.00307375 | synonymous-codon | USP12 | GRCh38.p7 | 13:27075388 | TTTTTTAACTTTCAT[C/G]CTATTAAAAATAAAA | 219333 |
rs781710307 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27105511 | AGAATTTTATCACTG[A/T]ATAACGCAATGCAAA | 219333 |
rs781712612 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118402 | TATAAAACCTTAATA[A/C]CATCACTAGTTAATA | 219333 |
rs781724979 | in-del | -/TGTG | | | intron-variant | USP12 | GRCh38.p7 | 13:27087252 | TATAGTGGGGAGGGA[-/TGTG]TGTGTGTGTGTGTGT | 219333 |
rs781751033 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139472 | AATACAAAAATCAGC[C/T]GGGCATGGGGCTGTG | 219333 |
rs781751943 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154417 | GTTCCACTGCATCTT[C/T]ACTTTTCTCCTGCTG | 219333 |
rs796072694 | in-del | -/AA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129165 | CTTACCACAATAAGA[-/AA]GTGACCTGTAGCTCT | 219333 |
rs796076571 | snp | C/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067952 | AACCCCCAACAGAAT[C/G]AAGTCTTAGCAAACA | 219333 |
rs796182853 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153907 | AGGCTCTATGTTTCA[C/T]CCTATTTCTCGTAAG | 219333 |
rs796191816 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152959 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAAGA | 219333 |
rs796289528 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27107119 | CACTTGAGGTTAGAA[A/G]TTCGAGACCAACTTG | 219333 |
rs796319103 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152759 | CATCCTGGTTAACAC[A/G]GTGAAACCCCGTCTC | 219333 |
rs796343994 | in-del | GA/TTTT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163111 | TACAAGCAAATTTTG[GA/TTTT]AAATCAATGTAATTC | 219333 |
rs796373719 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27095381 | ATCAAACAGTTCAAG[A/C]TACAGTAAGTATCTT | 219333 |
rs796384859 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27118892 | CATGTCCACCTGTCA[C/T]CATATGTACCACATA | 219333 |
rs796397655 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27107216 | TGTGATTCCAACTAC[G/T]CAGGAGGCTGAGGTA | 219333 |
rs796464039 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162187 | GACGTTCACATGTGT[C/T]ATCTCATCTGATCTA | 219333 |
rs796477499 | in-del | -/ATAC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150209 | CACTGTACCCCACAA[-/ATAC]ATACAATTATGTCAA | 219333 |
rs796510986 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136367 | GCCGGGCATGGTGGC[A/G]CATGCCTGTAATCCC | 219333 |
rs796511449 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162851 | TTTTTCCTATTTTCC[C/T]TCCCTCAGAGTTTGA | 219333 |
rs796559473 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27091191 | ATGATATGTTTAAGG[-/A]AAACACATCAATTTT | 219333 |
rs796611544 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144218 | AAAAAAAAAGTGTCA[A/G]CCAAGTGTGTGGCTC | 219333 |
rs796662071 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148362 | TAATTGATTTAAAAA[A/G]CAACTGTATAAAACT | 219333 |
rs796688446 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27105578 | TCTCCTTCACTAAAC[A/G]AGTGCCTCTTTGAAG | 219333 |
rs796706918 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27097968 | CCTTATAGCCTGGAG[A/G]TAACTTTATATAGTA | 219333 |
rs796717083 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154457 | GTGTGCTAACAGTAC[C/G]TGAAGTAAAAATTCT | 219333 |
rs796723630 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27082110 | CCTGTCCTTTGAAGC[A/T]GGGCGCTCACTTCTC | 219333 |
rs796760321 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27105085 | ATTAACCTCTCTGAG[C/T]CTCAGTTATTTCATA | 219333 |
rs796763711 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153937 | GTTTACTGAGGTATC[A/G]AATCTAATTATGGCA | 219333 |
rs796771978 | in-del | CGCGCACGCTC/TGTGTGTGT | | | intron-variant | USP12 | GRCh38.p7 | 13:27087270 | TGTGTGTGTGTGTGT[CGCGCACGCTC/TGTGTGTGT]TGTGCGCGCACGCTC | 219333 |
rs796810513 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27123106 | CAAAAAAAAAAAAAA[-/A]TATTTTACAGAGAAG | 219333 |
rs796826220 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27088674 | CACTCAGTCTGTAAT[C/G]AGCTTCCTGTGTTGT | 219333 |
rs796854136 | in-del | -/ACCT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168118 | TGGGACTCTCCTAGC[-/ACCT]ACCTTTACCAGCTTT | 219333 |
rs796864280 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150894 | CCTCAAACCATGTAC[-/A]AAAAACTAACTCCAA | 219333 |
rs796865963 | snp | C/T | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069020 | ATGACTGGAAGGCTG[C/T]TTTAAAAGAGGAGCT | 219333 |
rs796869615 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27097423 | TGAGCCGAGATTGCG[C/T]CATTGCACTCCAGCC | 219333 |
rs796884433 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27114771 | TCCTCTCCATTTTTA[A/T]AAAAAAAAAAAAAAC | 219333 |
rs796946744 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138214 | GAAGAATACTGCTAC[-/C]ATCCATTTAACTATA | 219333 |
rs796999276 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137940 | GGCCTCTCAGCACTG[A/G]GGGCAGCTGCCAACT | 219333 |