SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9713 | snp | A/T | 0.46865 | 0.121211 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161308497 | CGCCGGTTTGCAGAC[A/T]GAGCCGCGTCGGGTG | 10213 |
rs1064576 | snp | A/G | 0.0569829 | 0.158885 | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411597 | TTTGCAGATTCTAAA[A/G]TTATACATGAATACA | 10213 |
rs1110587 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407766 | CACCACCATCTCACC[C/T]CCTTTTGTAACTCTT | 10213 |
rs1111416 | snp | C/T | 0.11963 | 0.213316 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355716 | GTTTTAAAACATAAA[C/T]GAGTTAATACACCTT | 10213 |
rs1111417 | snp | C/T | 0.121717 | 0.214577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352474 | GTGTAGTTTATTATT[C/T]TAGTGGCAAAATAAA | 10213 |
rs1116165 | snp | A/G | 9.73492e-05 | 0.00697604 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318779 | TTCCTAAGCACAAAA[A/G]TGTTTATTCAATTGC | 10213 |
rs1116173 | snp | C/T | 0.386123 | 0.209692 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370327 | GATATACTAGACAGG[C/T]GGTGCATGGCACTGA | 10213 |
rs1136548 | snp | C/T | | | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161316490 | ACCTGCCAGAATTAG[C/T]AAGAGCTTTCTTTAA | 10213 |
rs1559496 | snp | C/G | 0.470327 | 0.118136 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358583 | TCATTAATCTGACCA[C/G]TCCTACTCTACATTT | 10213 |
rs1862953 | snp | A/T | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350294 | GTATGTCCCAAATAC[A/T]GCCTGGGATGTACTT | 10213 |
rs1863177 | snp | A/T | 0.244205 | 0.249933 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401288 | CAGTAAGGCTTTCAG[A/T]CAACAGTAGGCTATT | 10213 |
rs1882366 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406627 | AGATATTCCAAATCA[A/T]ATGCCTACATATTTT | 10213 |
rs1921674 | snp | C/T | 0.245061 | 0.249951 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391261 | TATGTGATTTAAATT[C/T]GAATTTTTGACCTCT | 10213 |
rs2013879 | snp | A/G | 0.352287 | 0.228117 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319533 | ATGACTGCACAGATC[A/G]AAAGTGTCGAACTCA | 10213 |
rs2018759 | snp | A/G | 0.295088 | 0.245901 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407704 | ATTATAAAGTTCAGA[A/G]TATCCAAATCTAACC | 10213 |
rs2042488 | snp | A/G | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344180 | tactgagggatgact[A/G]TACTCAGAAGTGAAG | 10213 |
rs2042489 | snp | A/G | 0.261884 | 0.249717 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368658 | CTTAGAAAAATATGC[A/G]TGTATTTTTCCAAGC | 10213 |
rs2059337 | snp | A/G | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310502 | TCATTTTGACATTTC[A/G]TATTCTGCTTTGTGT | 10213 |
rs2113480 | snp | C/T | 0.383824 | 0.211166 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330099 | TGCAATTATGATAAA[C/T]AAATTTGTTCAAGTT | 10213 |
rs2194726 | snp | C/T | 0.135825 | 0.222405 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389321 | AAGCTCCACTCTCTA[C/T]GCCAGACTATGTCTG | 10213 |
rs2194727 | snp | C/G | 0.135484 | 0.22223 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389360 | ACTGAGCACCTTTTT[C/G]TAATTCTCTACCAGG | 10213 |
rs2194728 | snp | A/G | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389513 | TGATTATTGAAATGA[A/G]TAAGGATTTAATATA | 10213 |
rs2194729 | snp | C/T | 0.233235 | 0.249437 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392937 | TCAATTTTTCTTTCT[C/T]TTTTTTTGGGGAGTA | 10213 |
rs2216941 | snp | A/T | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402194 | TCTCCAGTCTTTCCC[A/T]TTCAAATCAATTTTC | 10213 |
rs2278077 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161308800 | AGGTCTGGATGTCGC[C/T]TCCTTTCTCCATTCT | 10213 |
rs2288099 | snp | A/G | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367744 | GAACCAGAGACCTCA[A/G]CGAAATTTGCTTTGT | 10213 |
rs2303318 | snp | A/C | 0.339203 | 0.233544 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367984 | AAACTAACTCTCATC[A/C]TATTACATTTTCTCT | 10213 |
rs2303319 | snp | C/T | 0.132066 | 0.220435 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368153 | GTCCTTCGGCTTAAA[C/T]TGGTGTAAAATACTG | 10213 |
rs3207471 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339518 | TTGAGTAGATGATCT[A/C]AAAAAAAAAAAAAAA | 10213 |
rs3213812 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316611 | TTAATTATTATTTTA[C/T]GGATGGATAGAGAGA | 10213 |
rs3769957 | snp | A/T | 0.489837 | 0.0705577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407333 | TCTAGACAGAGAATA[A/T]GCTCATTTTCAGAGT | 10213 |
rs3769958 | snp | A/G | 0.241627 | 0.24986 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404878 | CAGAAGAGCAGAAAG[A/G]CAAGGGCTGAATCTT | 10213 |
rs3769959 | snp | C/T | 0.135825 | 0.222405 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392695 | TAGAAGAGAGCATTA[C/T]AAGATCCCCTTGCGC | 10213 |
rs3769960 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386279 | TAATCTTTAGAGTAG[C/T]AATTAACTAGATAGA | 10213 |
rs3769961 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356660 | TTTTTAAAAGTCTGT[G/T]AAAATATATGCTTTA | 10213 |
rs3769962 | snp | C/T | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351070 | ATTCAAACAAATGAA[C/T]AGAGTAATAAATTCC | 10213 |
rs3769963 | snp | C/T | 0.320814 | 0.239761 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350999 | ATTTACTAAGGGAGA[C/T]TGGACAAAGGAGGAC | 10213 |
rs3769964 | snp | A/G | 0.148326 | 0.228391 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350835 | GTTTTGCCTTAGGCA[A/G]CAGAGTAACTATCAA | 10213 |
rs3769965 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332139 | ATAAAGAAAATCCCT[C/T]CTAAATATTTTAATT | 10213 |
rs3769967 | snp | A/G | 0.25801 | 0.249872 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318062 | TGATTTAGTTTTAAC[A/G]TTTAGAGTAACTACA | 10213 |
rs3769968 | snp | G/T | 0.329783 | 0.236927 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309640 | AACCACTATATATCT[G/T]AACCTCTAAACTTCA | 10213 |
rs3835938 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390831 | GTCAGAGATAAGGTT[-/T]GATCTTATCATAAGC | 10213 |
rs3841876 | in-del | -/ATTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161330100 | TAAGAACTTGAACAA[-/ATTT]ATTTATCATAATTGC | 10213 |
rs4027148 | in-del | -/AT | 0.0460142 | 0.144533 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319036 | GCAACACTAGATAAC[-/AT]GTGGAAAACATTTAT | 10213 |
rs4027149 | snp | C/T | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340634 | GGGCCAAAGGTGTTC[C/T]CAGGATCCTGCTAGC | 10213 |
rs4027150 | in-del | -/T | 0.0766824 | 0.180169 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356777 | AAATATTCAAACTCC[-/T]TTTTTTTTTTTTTTA | 10213 |
rs4027152 | snp | A/G | 0.466927 | 0.124269 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402911 | AATGAAAAATAACAA[A/G]TGTTGCCAAGGGTAT | 10213 |
rs4119067 | snp | C/G | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340294 | CAACCAAGCCAGCCA[C/G]AGAGAGAAGTGGGTT | 10213 |
rs4119068 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161340434 | AGGGCAAAAGAGGGG[A/G]GACTGGAGTGAAAGT | 10213 |
rs4119069 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161340472 | GCTTTTAAAATGTTC[G/T]TTTTATCTAAGGTGT | 10213 |
rs4664044 | snp | G/T | 0.255503 | 0.249939 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313120 | ggaggagagaggtaa[G/T]ttactcaaggacagg | 10213 |
rs4664417 | snp | A/G | 0.46885 | 0.12085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322682 | GATGTGAACCATTGC[A/G]CCCGGCCTGGTCATG | 10213 |
rs4664418 | snp | C/T | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337530 | TGGTCTTTCTAATTC[C/T]AAAGTATCTCTGCAC | 10213 |
rs4664419 | snp | A/G | 0.492727 | 0.0598633 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344554 | AGAAAGTGTCATATT[A/G]TTTTTCACAGCGAAT | 10213 |
rs4664420 | snp | A/G | 0.466618 | 0.124806 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364414 | ggaaatgcaacattt[A/G]gggaggaaaacaaaa | 10213 |
rs4664421 | snp | A/G | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372550 | CTATCCACAAAAACA[A/G]TAATAGAAACTGATA | 10213 |
rs4664422 | snp | C/G | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392317 | GTTAGTGAGACCGCT[C/G]TCAAGTCAGAAAGTG | 10213 |
rs6432678 | snp | A/G | 0.121717 | 0.214577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351502 | ATATTACTTTTTGTA[A/G]GGTGTTCTCTGTAAA | 10213 |
rs6432679 | snp | C/T | 0.493613 | 0.0561475 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351747 | CTGGGTGCTCTGTTC[C/T]GTGGTATCATTACTG | 10213 |
rs6432681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410650 | TAAAGGATTGCACCT[A/G]TATAATTTGCTATGA | 10213 |
rs6709356 | snp | A/G | 0.492679 | 0.0600586 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355219 | CCTAGGTATATTTCA[A/G]CAGTGGGTGAAATTA | 10213 |
rs6710414 | snp | G/T | 0.338523 | 0.233803 | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161412004 | AGGATTTTGGAAGAG[G/T]ACATTTACAAAGAAA | 10213 |
rs6710747 | snp | C/G | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320179 | GGTGGTATGTAGATA[C/G]TGCAGATTTACCTGC | 10213 |
rs6713728 | snp | C/G | 0.121717 | 0.214577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326290 | cccacctcggcctcc[C/G]aaagtgctgggatta | 10213 |
rs6713971 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326454 | tcttgtacattgatg[A/G]tagaaatgtaaaatg | 10213 |
rs6719721 | snp | G/T | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374009 | AAAAATTAGGGCCAA[G/T]GAGATTGCTTTGCCA | 10213 |
rs6722186 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358824 | catgtacctgtaatc[C/T]cagctacttgggagg | 10213 |
rs6723514 | snp | A/C | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316680 | ATGAATGTGATTGAT[A/C]ACCAGATTTTGAAAA | 10213 |
rs6725325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364925 | cctgggcaacacagg[A/G]aaaccccatccctac | 10213 |
rs6727917 | snp | A/G | 0.4661 | 0.125701 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378097 | GGACTTAGTTTTGTC[A/G]GGTTTAATGTCTTCT | 10213 |
rs6733456 | snp | C/T | 0.48955 | 0.071525 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401922 | GTGTATGGCTAGAGG[C/T]AAGTCAGCCTCTCTG | 10213 |
rs6734935 | snp | C/T | 0.121717 | 0.214577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323068 | TTAAACCTTTTCTTC[C/T]ATTTATTTCTAGAAT | 10213 |
rs6738264 | snp | C/T | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383743 | CTCCTAAATATTTAC[C/T]GTTAACAGTTAGGGT | 10213 |
rs6738798 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333077 | AGCATCTGTCTTGTA[C/T]ATTTTTGAAGGATTT | 10213 |
rs6744214 | snp | C/T | 0.468349 | 0.121752 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335777 | GTAGTTAGCCTGATA[C/T]GGTAGAAAGAATACA | 10213 |
rs6748704 | snp | C/T | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331208 | TGTGATTTCTGGTTA[C/T]TGTATTCATTTCCTG | 10213 |
rs6755769 | snp | G/T | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347191 | ttgttgcttgatcag[G/T]gtcttacaaactatt | 10213 |
rs6755815 | snp | C/T | 0.257176 | 0.249897 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347385 | aactactcaaggaat[C/T]ctcctgctccagtct | 10213 |
rs7349280 | snp | C/T | 0.303438 | 0.244222 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354120 | TGTTCTGTTATGAGA[C/T]GTTCAGGTTCTGCTT | 10213 |
rs7421731 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161355569 | gtctttctttttttc[C/T]ttTAAAGAATTAATG | 10213 |
rs7566586 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351912 | tagggaagtgcagtc[C/G]tactatgtgcctgag | 10213 |
rs7574882 | snp | C/T | 0.223225 | 0.248562 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399267 | TAGTAAGAATATTAA[C/T]GTGAGCTTTGAAAAA | 10213 |
rs7578146 | snp | C/T | 0.121369 | 0.214369 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405831 | TGGCATGTTATAGTG[C/T]GAACAAAGTTAACAT | 10213 |
rs7586485 | snp | A/G | 0.244205 | 0.249933 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402429 | aggatcatcacttga[A/G]cccaggagttcaagg | 10213 |
rs7589726 | snp | A/C | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338203 | CCTAGAATTTCTCTC[A/C]AAGAATCCTTGGAAC | 10213 |
rs7595718 | snp | A/G | 0.121717 | 0.214577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352199 | AAGTTTATATCAGTG[A/G]TTTTCAACCTTGGCT | 10213 |
rs7605885 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312971 | GATGGGGTTGCCAAT[A/G]acagtagctagtgtt | 10213 |
rs10170291 | snp | A/T | 0.474544 | 0.10991 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313357 | attaattaattaatt[A/T]atttatttttgagat | 10213 |
rs10174431 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344566 | Attgtttttcacagc[A/G]aatgattatctttta | 10213 |
rs10182431 | snp | A/G | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341878 | aaaaaaaatatatat[A/G]tatatataaatttgt | 10213 |
rs10193429 | snp | C/T | 0.122411 | 0.214991 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385715 | AGAATTGTGGAAATA[C/T]TGTTGTAAAAATTAG | 10213 |
rs10197817 | snp | C/T | 0.470132 | 0.118498 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342482 | ttggttgatataata[C/T]aggcgttcagctttc | 10213 |
rs10206910 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389879 | tgtcttattttcttt[C/T]tttTTTGTTGTTTTT | 10213 |
rs10207096 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389886 | TTTTCTTTCTTTTTT[G/T]TTGTTTTTTTTTTTT | 10213 |
rs10207098 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389889 | TCTTTCTTTTTTGTT[G/T]TTTTTTTTTTTTTTT | 10213 |
rs10210533 | snp | C/T | 0.491577 | 0.0643472 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311171 | aaaattagccgggca[C/T]gggggcgtgtgcctg | 10213 |
rs10469684 | snp | G/T | 0.46855 | 0.121392 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326996 | agaaacctgttgata[G/T]ggagggctgattgta | 10213 |
rs10490567 | snp | C/T | 0.3512 | 0.228601 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317267 | GTTAAGATCGTGAAG[C/T]GGAAATTTTGTCTGT | 10213 |
rs10490568 | snp | A/G | 0.131381 | 0.220067 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395910 | AACACCTTCATATTC[A/G]GATTGTCCACACACC | 10213 |
rs10497214 | snp | A/C | 0.245916 | 0.249967 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369825 | ACGAAATAATTGAAC[A/C]AACCATAACTATTGG | 10213 |
rs10561352 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161356763 | AAATATTCAAACTCC[-/T]TTTTTTTTTTTTTTT | 10213 |
rs10579763 | in-del | -/TTC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344634 | TTAACATTTCTGGTG[-/TTC]TTCTTTTTATTGTAT | 10213 |
rs10649473 | in-del | -/CTTA | 0.145145 | 0.228506 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354508 | GCATTGTGCTTGGTC[-/CTTA]CCTTGTTGCAGTGGA | 10213 |
rs10663730 | in-del | -/ACTT | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354511 | TTGTGCTTGGTCCTT[-/ACTT]GTTGCAGTGGAGCAC | 10213 |
rs11311339 | in-del | -/A | 0.227369 | 0.248974 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402699 | AGAATTAAAAACAGG[-/A]AAAAAAAAAAGAAAC | 10213 |
rs11412874 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357904 | TTCTTTTTTTTTTTT[-/T]AATGGTGGTGAAACA | 10213 |
rs11429061 | in-del | -/A | 0.121717 | 0.214577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323940 | CGTTGTCTTTATAAC[-/A]AACTCCACCTAGGTC | 10213 |
rs11449569 | in-del | -/A | 0.121717 | 0.214577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362269 | TGTTTCCAGAATAGT[-/A]AAAGTCAACACTTAC | 10213 |
rs11452254 | in-del | -/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393971 | TTTTTTTTTTTTTTT[-/T]GGAGTCTCACTCTGT | 10213 |
rs11546859 | snp | A/G | | | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161367789 | ACTGTTAAAAATGTT[A/G]AAACATGGCCGTGCT | 10213 |
rs11675219 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349882 | GATTAATGAATAATT[A/G]TGTTAGCATTTGGAG | 10213 |
rs11677317 | snp | A/T | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389854 | agaaacttggacaaa[A/T]taatatttgtgtctt | 10213 |
rs11680251 | snp | C/G | 0.363359 | 0.222822 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340115 | TTCTGCTATAGCAGA[C/G]TGGAGATTTGGCTGA | 10213 |
rs11680412 | snp | A/C | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370698 | CAAAAGGCTCAGCAG[A/C]TGAGCAGAACAGTGC | 10213 |
rs11682439 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389737 | AATAGACTTAATCCA[A/G]GAATTTCCTGACATG | 10213 |
rs11685006 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343485 | cagttgggttgattt[C/T]accttttggctattg | 10213 |
rs11693813 | snp | A/G | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389738 | ATAGACTTAATCCAA[A/G]AATTTCCTGACATGT | 10213 |
rs11883852 | snp | G/T | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387679 | ATATTTTATAGATGG[G/T]GCCTATATATTTATA | 10213 |
rs11885856 | snp | A/C | 0.121717 | 0.214577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327885 | AGATTAGTTAAAAAA[A/C]AAACAAACCTGTGGA | 10213 |
rs11885894 | snp | A/G | 0.121717 | 0.214577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327810 | GAATGGCCAAAAAAA[A/G]TTATGAAAAGATAGT | 10213 |
rs11886577 | snp | C/T | 0.439224 | 0.163383 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394926 | TTATATTAATACAAA[C/T]ATAGGAGCATTCTAA | 10213 |
rs11896707 | snp | A/T | 0.48498 | 0.0853497 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327985 | GTGTGTGTGTGTGTG[A/T]GATGTTGGTTAGGAA | 10213 |
rs12105834 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389991 | tgcctcagcctccca[A/G]agtgctgggattaca | 10213 |
rs12463483 | snp | G/T | 0.135484 | 0.22223 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396108 | CTGACTTTCAAGCTG[G/T]CCAACACCCAGGTTG | 10213 |
rs12463535 | snp | C/G | 0.135484 | 0.22223 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396388 | aacctaagtgtcaat[C/G]aacagacagataaag | 10213 |
rs12467117 | snp | G/T | 0.135825 | 0.222405 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369804 | TGCTTGCCTAAATAG[G/T]TCTAACCAATAGTTA | 10213 |
rs12471336 | snp | G/T | 0.131381 | 0.220067 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408678 | TTTATTGCCCTGAAG[G/T]TTATTCTGAAGTTTA | 10213 |
rs12471658 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403816 | AGCCTAACCCTTTCT[C/T]ACTTTTGAGACCCTC | 10213 |
rs12473980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311022 | ggaaaaaagttgcat[C/T]taggccaggcgtggt | 10213 |
rs12624268 | snp | A/C | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348909 | GAAATAAAGTAAATA[A/C]CAGTGGTTAGAAAAA | 10213 |
rs12988044 | snp | A/G | 0.079617 | 0.182947 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336398 | GCTGATACTATTTAC[A/G]AGCAGCTGTAGGTTC | 10213 |
rs13002631 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389887 | tttcttTCTTTTTTG[G/T]TGTTTTTTTtttttt | 10213 |
rs13016002 | snp | G/T | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391466 | TTTCTTTTAGTTCTG[G/T]GATTTTTCTGATTAA | 10213 |
rs13024569 | snp | A/G | 0.294832 | 0.245947 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331289 | TATTTTTAAGACGGA[A/G]TCTCACTCTGTTGCT | 10213 |
rs13031720 | snp | G/T | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356978 | ACACTAAGAGAAAGG[G/T]GGAGTAATATAACTA | 10213 |
rs13384725 | snp | A/T | 0.121717 | 0.214577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409359 | TTCACTTTTCTAAGA[A/T]GAAATATATATTTTA | 10213 |
rs13398392 | snp | C/T | 0.43309 | 0.17023 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330739 | TTTTAAGCTGTTGCC[C/T]GTGATTGCACAGGCT | 10213 |
rs13403207 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368225 | TGATTTTGAACCAAG[C/T]GTTCAAAAGATTTGA | 10213 |
rs13414363 | snp | G/T | 0.437542 | 0.165312 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315501 | aaagactacagagat[G/T]aagtctctagtgttc | 10213 |
rs13430019 | snp | A/G | 0.438526 | 0.164189 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365183 | ATGGCTTTCTTGTTA[A/G]TATGTTTCTGAATCA | 10213 |
rs16845764 | snp | A/C | 0.0955749 | 0.196603 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307874 | AACTAAACTCGGCTT[A/C]AAATAGGTGGTTTGA | 10213 |
rs16845770 | snp | C/T | 0.312348 | 0.242101 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325276 | GAATGTGGTGAGATA[C/T]AGTGTACATTTTGAA | 10213 |
rs16845807 | snp | A/G | 0.135825 | 0.222405 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390888 | TTTGTGCTCCTCCAT[A/G]TCATGCTTTGAAGAA | 10213 |
rs16845810 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392891 | ACTGATATCTGACAC[C/T]CATCTATTTGGAAAT | 10213 |
rs16845811 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394325 | GCTTTTCATCCTGAC[A/G]ATAAGGAAGTTTTAA | 10213 |
rs16845823 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397968 | AATTATTCAGCAGAC[A/T]GTAGGAATGGTTTTC | 10213 |
rs16845825 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | PSMD14 | GRCh38.p7 | 2:161398415 | CAGTTTCAAGTCTGA[A/T]TTCCACACAAATTCT | 10213 |
rs16845829 | snp | C/T | 0.303688 | 0.244167 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399960 | AAATAATTCCTATCA[C/T]GTTATCTTCTCTCCC | 10213 |
rs16845830 | snp | A/G | 0.135484 | 0.22223 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401684 | TTATTATTCATCTCT[A/G]TTTCATGTAATTACA | 10213 |
rs16845844 | snp | A/G | 0.351853 | 0.228311 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408759 | AAAATTCTGGTCATC[A/G]TTATTTTTGGTGATT | 10213 |
rs17183625 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406964 | ACCATCTTTGTTGTT[G/T]GCAATATTCCGCAAT | 10213 |
rs17707401 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323107 | TAATAGCTTAAACTC[C/T]ATAATCTACTTAATT | 10213 |
rs17758464 | snp | A/G | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336370 | TATTGGTCGGAAACA[A/G]GGAAATGAAGATGCT | 10213 |
rs17758740 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354758 | GGTCTTAAAGGGAAA[A/G]AAATGTCATAGTTAG | 10213 |
rs28375809 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312174 | TTTGAGATGGAGTAT[C/T]GTTCTGTCACCCAGG | 10213 |
rs28637294 | snp | G/T | 0.116433 | 0.211329 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356048 | TGTCAGCCAAAGGAT[G/T]TTTTTTTGGAACATT | 10213 |
rs28807174 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314621 | TGGATATTTCATATA[C/T]ATGGAATCACATAAC | 10213 |
rs34015300 | in-del | -/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315860 | TTTTTTTTTTTTTTT[-/T]GAGACCGAGTTTCAC | 10213 |
rs34052325 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338322 | TAACGCAGTTATATT[-/T]GTAGGTAGGGTTAGG | 10213 |
rs34061827 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360381 | GTTTTTTTTTTTTTT[-/T]CACCCGCTCTGTCAC | 10213 |
rs34102562 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331824 | TGCTGAGTACCTTCC[-/C]TTATTCTGATATGAA | 10213 |
rs34156868 | in-del | -/TT | 0.123105 | 0.215401 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338342 | GTAGGGTTAGGAGAG[-/TT]TTTTTTTTTTTTTTT | 10213 |
rs34281870 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318781 | ATTGAATAAACACTT[-/C]TTGTGCTTAGGAACG | 10213 |
rs34311363 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161330146 | TTGGTGATAAATTTT[-/T]CAGTTACAGTGAAAC | 10213 |
rs34424898 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342334 | AGACTTTTTTTTTTT[-/T]ATCAGAAGTGGATCT | 10213 |
rs34494874 | in-del | -/T/TC/TTC | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361468 | ATAGATTTTTTTTTT[-/T/TC/TTC]CACATACATATTATT | 10213 |
rs34548198 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383671 | TTTGTAGTAGCTTTT[-/T]CTCCCTCTCACAAAT | 10213 |
rs34583707 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404533 | TGCCCCTCTCCCTTC[-/C]TTGAGGCTAACTGGA | 10213 |
rs34635738 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311649 | TTTTTTTTTTTTTTT[-/T]GAGATGAAACCTTGC | 10213 |
rs34697002 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358558 | TGCCCATTTCTGCCC[-/C]ATTACAACCTCATTA | 10213 |
rs34698460 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386847 | TGCAAGTCACTCACC[-/C]ACCTGTTGCAGATTT | 10213 |
rs34704139 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354632 | TTTCACACACACATA[-/A]GAAACTTTGTTTTTA | 10213 |
rs34742569 | snp | C/G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161374965 | TCCTAACAATCATTG[C/G/T]GTCTGTTCTCTGTTT | 10213 |
rs34752550 | in-del | -/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347933 | GAGCTACGGCTTGGG[-/G]AAAGTTTTATCTAAC | 10213 |
rs34801209 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392134 | TAATGCCAAGTATTT[-/T]AAATCTGCCTGTTGT | 10213 |
rs34824476 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161387386 | CAGAAATGCCATGCC[-/T]TTTTATTTTGAAGGG | 10213 |
rs34830575 | in-del | -/ATT | 0.286791 | 0.254975 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401778 | ATTATTATTATTATT[-/ATT]CAGGTTGTATCAGTG | 10213 |
rs34853866 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321198 | AAAGGCAGAATTCCC[-/C]TCCCAAATAGGAGCA | 10213 |
rs34875529 | snp | A/C | 0.0452528 | 0.143452 | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161412047 | TAATTTAGACTTTAT[A/C]ATGTTTTAAAAGAGT | 10213 |
rs34878108 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161370814 | GTTAAAAATGTACTC[-/C]TGTGCCTGGAAAATC | 10213 |
rs34989714 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161370062 | TAGGGAAGCTTTTTT[-/T]CCAAATTTACAAAAA | 10213 |
rs35153243 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161409295 | AGAAAGGTTAGAGCC[-/C]TTATTGGGTTATACT | 10213 |
rs35212116 | in-del | -/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391687 | CCTTGAACTTTTAGG[-/G]CCCAAGGGATCCTCA | 10213 |
rs35338761 | in-del | -/AA | 0.121369 | 0.214369 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343828 | GTGATACTCTGTCTC[-/AA]AAAAAAAAAAAAATG | 10213 |
rs35374285 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396055 | AGAAACACTACCATA[G/T]AGAAGACCATGGGAA | 10213 |
rs35378537 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352652 | TTTTCTTCCTTTTTT[-/T]CAAATAGTCGTGCCC | 10213 |
rs35436319 | in-del | -/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345531 | TCCCAAAGTGCTGGG[-/G]ATTATAGGCATGTGC | 10213 |
rs35453504 | in-del | -/CT | 0.121022 | 0.21416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384547 | CAAAATATAGAAATA[-/CT]CTGTTACTTAGTATA | 10213 |
rs35483490 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318926 | AACTACAAGCCTTTT[-/T]GTAGTTAGCCAAAGA | 10213 |
rs35518984 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161411032 | GCTGTATAGAATTCC[-/C]TTGTTACTCTTTATA | 10213 |
rs35571654 | in-del | -/CA | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399386 | TTTTTACCTATAACA[-/CA]GAGTGAGCTAGTATC | 10213 |
rs35590291 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398656 | AATTTGCCTTTTTTT[-/T]CCCAAGCATGTAGTG | 10213 |
rs35667315 | snp | G/T | 0.0222194 | 0.103034 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409890 | GTGATATCACCCTTG[G/T]TATCTTTTCCACTAC | 10213 |
rs35727348 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405320 | GATCCACAAGAAAAA[-/A]GTTAGGTACATTTAC | 10213 |
rs35792400 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344238 | TTGGGGGTGTTCTAA[-/A]CAAATTACCATAGAT | 10213 |
rs35808781 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321202 | GCAGAATTCCCTCCC[-/C]AAATAGGAGCAGGTC | 10213 |
rs35876321 | in-del | -/T/TTT | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360207 | TTTTTTTTTTTTTTT[-/T/TTT]GAGACAAGGCCTCAC | 10213 |
rs35898739 | in-del | -/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336934 | GCTCATTTTAAGTTT[-/G]TCCTTGACTTCATTT | 10213 |
rs35907319 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383901 | ACTTCTATATTTTTA[-/C]ACAATTGTTTGAAGT | 10213 |
rs36103526 | in-del | -/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322582 | TTAGTAGAGGTGGGG[-/G]TTTCACCAAGTTGGC | 10213 |
rs36104426 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318282 | ATGAGTTCAGTTTTT[-/T]AAAAGCCTTTGATGC | 10213 |
rs36202166 | in-del | -/ACACAC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366388 | AAGTAATAGAATTTA[-/ACACAC]ACACACACACACACA | 10213 |
rs41264223 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407995 | TGGTGCCATTATTGG[C/G]AGAGGAGGGCAGTAG | 10213 |
rs55819394 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389916 | TTTTTTTTTTTTAGA[A/G]ATGGGGTATTGCTAT | 10213 |
rs56265053 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161362265 | ATTTATGTTTCCAGA[A/G]TAGTAA | 10213 |
rs56314328 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361698 | GATGATTTAATAGTG[A/G]GAAATATTAATGTAA | 10213 |
rs56792517 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392275 | AGAACACTGAGTTTA[C/T]TGTTGATTGATAGCC | 10213 |
rs57029628 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315863 | TTTTTTTTTTTTTGA[A/G]ACCGAGTTTCACTCT | 10213 |
rs57090160 | snp | A/G | 0.160609 | 0.233472 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322686 | TGAACCATTGCGCCC[A/G]GCCTGGTCATGTTTT | 10213 |
rs57275564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369127 | TAAAACTAACTTATA[C/T]ATGTTATGGGTACTT | 10213 |
rs57407438 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388067 | GTAACTAAATTTTTT[-/T]AAACTATTCCATTAT | 10213 |
rs57629301 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386519 | CTGTAATCTTCATCA[A/G]AGTGAAGTGTTTTGT | 10213 |
rs58162668 | in-del | -/T | 0.150667 | 0.229419 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367682 | CATTTATAAAAGGAG[-/T]TTTTTATTTTCACTG | 10213 |
rs58235295 | in-del | -/TCTC | 0.148661 | 0.22854 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319341 | TGGATTAATAAGTAA[-/TCTC]TCTCCTTTAAATTTG | 10213 |
rs58521726 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372955 | TGATGGTGGCTACTT[G/T]GAAAAAGGAAAGTAT | 10213 |
rs58627659 | snp | C/T | 0.131723 | 0.220251 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394399 | TGAGATTACCTAATA[C/T]AAGCCCCTTAATTCA | 10213 |
rs59234742 | in-del | -/GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389891 | TTCTTTTTTGTTGTT[lengthTooLong]TTTTTTTTTTTTTTT | 10213 |
rs59573635 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352116 | CCTCTGAAATTCCTA[A/G]ACAACTGGCTGGACA | 10213 |
rs60180746 | snp | A/T | 0.0733688 | 0.176922 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388427 | ACCAGACTGCTTCAT[A/T]CTTTTATATTATCAT | 10213 |
rs60327518 | snp | G/T | 0.444444 | 0.157135 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389892 | TTCTTTTTTGTTGTT[G/T]TTTTTTTTTTTTTTT | 10213 |
rs60598854 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365751 | TATGGAGTGATCACA[C/T]AAGGCTAACATATCC | 10213 |
rs60767767 | snp | C/T | 0.148661 | 0.22854 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329047 | TCTTTAATTTGAAGG[C/T]GATAATACTAGAGAG | 10213 |
rs61151010 | in-del | -/TTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338356 | GTTTTTTTTTTTTTT[-/TTT]GGAAAGAAAAACTTC | 10213 |
rs61247163 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331274 | TTTTTTTTTTTTTTT[-/T]ATTTTTAAGACGGAG | 10213 |
rs61626956 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400557 | CCAGAATTATTATTT[G/T]TATTTTTATTATTAA | 10213 |
rs62188121 | snp | C/T | 0.136166 | 0.22258 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375574 | CTCATGGGAAGAATG[C/T]AGAAACAATATCATT | 10213 |
rs62188122 | snp | A/T | 0.135484 | 0.22223 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383896 | AATTTTACTTCTATA[A/T]TTTTAACAATTGTTT | 10213 |
rs62188123 | snp | C/T | 0.316968 | 0.240864 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385335 | GTTCTTTTTTATTAA[C/T]ATTATAATTAAATGA | 10213 |
rs62188133 | snp | C/T | 0.131381 | 0.220067 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396924 | CATCTGTCTCCTGTG[C/T]TCAAGAGATTCTCCT | 10213 |
rs62188134 | snp | G/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397519 | GAAGCAATTAGAATG[G/T]GGGACTAGGAATTAA | 10213 |
rs62188135 | snp | A/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397525 | ATTAGAATGTGGGAC[A/T]AGGAATTAATGGTAA | 10213 |
rs62188136 | snp | A/G | 0.33875 | 0.233717 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399439 | GAATTCCTATAAAAT[A/G]TTTATTTTATTTTTG | 10213 |
rs62188137 | snp | C/T | 0.135484 | 0.22223 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401037 | TTGAATTGCTTGATA[C/T]GTACTATAGATAGAG | 10213 |
rs62188138 | snp | C/T | 0.33875 | 0.233717 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410935 | CAGACATTCAAGATA[C/T]ATGAACGGTAGAGAA | 10213 |
rs62194488 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342705 | AAATTATTGAATGTC[A/G]TTAAGTTTAAATCTT | 10213 |
rs62194489 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343556 | TTGAGGATCGGGTAC[A/T]GTGGCTCACGCCTGT | 10213 |
rs62194490 | snp | C/T | 0.3512 | 0.228601 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344287 | GATATTCATTTCTCA[C/T]AGTTCTGGAGGCTGG | 10213 |
rs62194491 | snp | A/G | 0.148996 | 0.228688 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348550 | TGTAAAGTATTGAAA[A/G]ATGAATAATCCTCAC | 10213 |
rs62194492 | snp | A/C | 0.144632 | 0.226711 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359052 | CAGCTCACTACAGCC[A/C]CAGCCTCCTGAGCTG | 10213 |
rs62194493 | snp | A/G | 0.135143 | 0.222054 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362103 | ACAGGGTCTCACTCT[A/G]TTGCCCAGGCTGGAG | 10213 |
rs62194494 | snp | A/C | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372452 | AATGTTTTCTGACAT[A/C]ATGTCATTATCATGT | 10213 |
rs62197074 | snp | C/T | 0.147656 | 0.228091 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312196 | TCACCCAGGCTGGAG[C/T]GCGGTGGCGCGATCT | 10213 |
rs62197075 | snp | A/C | 0.312837 | 0.241974 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312613 | TTATTGTATGTATGA[A/C]ATTATGTTAGGTATA | 10213 |
rs62197076 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161319164 | GAAAAAAAAACCCTC[A/C]AAATAGCTTACTTCC | 10213 |
rs62197078 | snp | A/G | 0.148661 | 0.22854 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326443 | GAAATTAGAACTCTT[A/G]TACATTGATGGTAGA | 10213 |
rs62197080 | snp | C/T | 0.147991 | 0.228242 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336727 | ACTACAGGTGTGCGC[C/T]ACCATGCCTGGCTAA | 10213 |
rs62197081 | snp | A/G | 0.337614 | 0.234145 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336814 | CTCCTGGCCTCAGGT[A/G]ATCCACTGCCTCAGC | 10213 |
rs66493909 | in-del | -/ATT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401779 | ATCATGCATTTGACA[-/ATT]TTATTATTATTATTA | 10213 |
rs66854446 | in-del | -/CTTA/TTAA/TTACT/TTAT | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354509 | CATTGTGCTTGGTCC[-/CTTA/TTAA/TTACT/TTAT]TTGTTGCAGTGGAGC | 10213 |
rs66994977 | in-del | -/CT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161361469 | TAGATTTTTTTTTTC[-/CT]ACATACATATTATTG | 10213 |
rs67041117 | snp | C/T | 0.332337 | 0.236052 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361832 | GTTTTAATTGTTACT[C/T]GTAAGCAGCATACAC | 10213 |
rs67724321 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360192 | TATATATGCATGTAT[-/T]TTTTTTTTTTTTTTT | 10213 |
rs71281822 | in-del | -/AAAA | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357088 | TGTTGACTAAGTGCT[-/AAAA]AAAAAAAAAAAAGGC | 10213 |
rs71408173 | in-del | -/C | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329501 | TGAATATTCTGGTTA[-/C]CTTTTTTTTCTTTGA | 10213 |
rs71423093 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161308241 | TAGGGAGAGAAAAAG[A/G]AGGCGTCGGCGGGGC | 10213 |
rs71423094 | snp | A/C | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310597 | AAAATGATAATAATA[A/C]CAATTATAACAAGAA | 10213 |
rs71423095 | snp | A/G | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311799 | TTTATATTTTTAGTA[A/G]AGACCAGGTTTCGCC | 10213 |
rs71423096 | snp | A/G | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346826 | TCCAGTGCTGTGTGG[A/G]AGGTAGGTGTACTCT | 10213 |
rs72173679 | in-del | -/AC | 0.145978 | 0.227331 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366388 | AAGTAATAGAATTTA[-/AC]ACACACACACACACA | 10213 |
rs72214119 | in-del | -/TGGTCTCCACCTTTTATTCATT | 0.473266 | 0.112482 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336111 | TTAGGTTTGTAAATA[-/TGGTCTCCACCTTTTATTCATT]TGGTCTCCACCTTTT | 10213 |
rs72434504 | in-del | -/ATAA | 0.311369 | 0.242351 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330094 | TGATATGCAATTATG[-/ATAA]ATAAATTTGTTCAAG | 10213 |
rs72876083 | snp | C/T | 0.338523 | 0.233803 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327527 | ATACCCTTCCCCAAT[C/T]CCCCCATTTTTTGGG | 10213 |
rs72876099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344783 | ATAAGAGTTCTTTTT[A/G]TCTGTGGACACAAGC | 10213 |
rs72876102 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347794 | CTCACTGTGTGCCGG[C/G]TACTCTTCTAAGTAC | 10213 |
rs72877917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362435 | TGCATTCAGTGGTTG[C/T]AACAGATTTCTTTAT | 10213 |
rs72877940 | snp | A/G | 0.304438 | 0.244001 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403965 | TAGGCGGGCTGCATG[A/G]TACTATCATAGCTCA | 10213 |
rs72877941 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405520 | AACTTCTTTATTGAG[A/G]TGTTTTAAGGATTCA | 10213 |
rs72996996 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330673 | AGTGCCCTGAAAGTA[C/T]GCCACCAGAGCAGGG | 10213 |
rs72998914 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360019 | TAGTATGGGATTGGT[A/G]TCTATCACACATTTG | 10213 |
rs73971182 | snp | C/T | 0.067446 | 0.170804 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307296 | TTGGAAAAGCTGTTA[C/T]GGAGATTACACATTT | 10213 |
rs73971184 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329653 | GCTTAACTACAAATA[A/G]TGGTGATTTTGCTTT | 10213 |
rs73971185 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338900 | AATCAGTGGGATCAT[A/G]TAATAGGAACTCTTC | 10213 |
rs73971190 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401539 | GTTACAGCAGAAGAA[A/G]GGGAAGATGGACATT | 10213 |
rs74169403 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343160 | CAACCATCACTGCCA[G/T]CTGTCAGAACTTTTT | 10213 |
rs74269115 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380583 | CAGTAAGCAATTCTC[C/T]GAGGATGAAGAAAGA | 10213 |
rs74376717 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383177 | TATTTTCACAGTGCA[A/G]AAAGCAATTATAAAA | 10213 |
rs74564505 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359361 | ATTCTTTGAACTGGT[A/G]ATATATTTGAGAACT | 10213 |
rs74733151 | snp | C/G | 0.135484 | 0.22223 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395345 | TGCAGTTCATCTGGT[C/G]TGCAACTACTCACCC | 10213 |
rs74833452 | snp | C/G | 0.110872 | 0.20771 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315085 | TTTATATCAGTGGTT[C/G]TCAATTGAGAGTGAT | 10213 |
rs75008817 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312856 | TGCAAGTCCCTATCT[A/C]CAGTGTGATTTAGTA | 10213 |
rs75097508 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401422 | TCTCATTTGACAGAA[C/T]GTAGTTAAATGGACG | 10213 |
rs75145973 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383790 | CTATTTAAGTTATAT[A/T]CCTATCTTGGAAAAT | 10213 |
rs75266442 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363409 | TAAATTTGTTATAAT[A/G]CTTTTACCCTTGTTT | 10213 |
rs75303922 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161361015 | TTTAGAAATTTAGAT[C/T]ATGTTGGCAATTTTA | 10213 |
rs75308196 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331606 | AGGCTTTTGCCTTGG[A/G]AGCTTTCAACTTGAA | 10213 |
rs75693360 | snp | A/C | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343831 | ATACTCTGTCTCAAA[A/C]AAAAAAAAAAATGTC | 10213 |
rs75863761 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387872 | CAAAGGTTATTTTCA[C/T]GTTCATGTTTTATAT | 10213 |
rs75928055 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312848 | CTGCGAAATGCAAGT[A/C]CCTATCTCCAGTGTG | 10213 |
rs76007868 | in-del | -/TCTC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161319345 | TTAATAAGTAATCTC[-/TCTC]CTTTAAATTTGGTAT | 10213 |
rs76063526 | snp | A/T | 0.136166 | 0.22258 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374323 | ATTAATTGATTTTTT[A/T]AAATGTGTTGTTCAA | 10213 |
rs76148218 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366506 | AGTATAAATGGGAGA[A/G]AGAACATGGCTTACA | 10213 |
rs76281928 | snp | A/G | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310080 | AGGTGGAACCTGGGA[A/G]GTGGAGGTTGCAGTG | 10213 |
rs76294034 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336128 | GTCTCCACCTTTTAT[A/T]CATTTGGTCTCCACC | 10213 |
rs76434641 | snp | A/C | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306535 | TTGCACCAACCAACC[A/C]AATAATTCTGCCTTA | 10213 |
rs76711168 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384946 | TAAAGTCTTTCATAG[G/T]CACAAGAAGTAAAAG | 10213 |
rs76713361 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409381 | TATATTTTAGTCTCT[A/G]TTATCTGAGGGTGGG | 10213 |
rs76756028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324324 | CTTTGAATCAGTGAA[A/C]GCTAATGCTCATTGT | 10213 |
rs76778467 | in-del | -/T | 0.476138 | 0.236877 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361458 | AAAAACACGGATAGA[-/T]TTTTTTTTTTCACAT | 10213 |
rs76825570 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346427 | CAGTTTTAAAAACTT[C/T]TAAATGTCTTTGCTA | 10213 |
rs76857526 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337020 | TTTACTTTGGAAGTA[A/T]CTTATTCAAAGTCAT | 10213 |
rs76881312 | in-del | -/TT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383056 | AGGGCTTTTTTTTTT[-/TT]AATCTTACGGTGGCA | 10213 |
rs76888861 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360368 | AGCCTTTCATATTGT[G/T]TTTTTTTTTTTTTCA | 10213 |
rs77109640 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383045 | GAGTGCTCACTAGGG[C/T]TTTTTTTTTTTTAAT | 10213 |
rs77167711 | snp | A/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360364 | GCTGAGCCTTTCATA[A/T]TGTTTTTTTTTTTTT | 10213 |
rs77176359 | snp | G/T | 0.0955749 | 0.196603 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315333 | CTAATTTTATTGTCA[G/T]CATTAGAGACTAGAG | 10213 |
rs77276341 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318326 | CATAATCTGCTCACA[A/G]TGTCTTTCACATGTA | 10213 |
rs77303385 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386895 | CACTGCTTTTTAACC[C/T]TAAAAATCGACTGTA | 10213 |
rs77426242 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161361013 | TATTTAGAAATTTAG[A/C]TTATGTTGGCAATTT | 10213 |
rs77459771 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356634 | CCTAAAGCCTATTTT[A/C]TTTTTTGTTATAAAG | 10213 |
rs77570964 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161362269 | ATGTTTCCAGAATAG[A/T]AAAGTCAACACTTAC | 10213 |
rs77609198 | snp | C/T | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324634 | GATTTTCTTTCTTTC[C/T]TTTTTTTTTTTTTGA | 10213 |
rs77715957 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400983 | TGTCAAAATGTATAC[A/C]TACATAGATGTACAT | 10213 |
rs77772075 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365713 | ATATTGGTGGGGGGT[A/G]ATGTTTTGATAAATA | 10213 |
rs77814892 | in-del | -/AAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343840 | CTCAAAAAAAAAAAA[-/AAA]TGTCTTTGAGTCTCT | 10213 |
rs77848849 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161328202 | TATATGTCTATATCA[A/G]GAGACATGTTGAAGA | 10213 |
rs78317453 | snp | G/T | | | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411560 | CAGTTGTGCAATTAC[G/T]TCTGTTTCTTTAGTC | 10213 |
rs78349007 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383046 | AGTGCTCACTAGGGC[C/T]TTTTTTTTTTTAATC | 10213 |
rs78375464 | snp | G/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383402 | AATGAAAGCATCTCA[G/T]TTTATTAAGTTCTTG | 10213 |
rs78512290 | snp | G/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360366 | TGAGCCTTTCATATT[G/T]TTTTTTTTTTTTTTT | 10213 |
rs78602660 | snp | C/G | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385142 | TTAGGTAAAATTTAG[C/G]TGACAAACATATGCA | 10213 |
rs78781461 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336129 | TCTCCACCTTTTATT[A/C]ATTTGGTCTCCACCT | 10213 |
rs78825353 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161367682 | ACATTTATAAAAGGA[G/T]TTTTTWTTTTCACTG | 10213 |
rs78912214 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336126 | TGGTCTCCACCTTTT[A/G]TTCATTTGGTCTCCA | 10213 |
rs79010850 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324633 | AGATTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTG | 10213 |
rs79069024 | snp | A/C | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381622 | GACCTAGCAGTTGAT[A/C]TGAAAACACAAATTT | 10213 |
rs79218557 | snp | G/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325198 | CTGGTACAGACCTCA[G/T]TAATTTCAGGATGCA | 10213 |
rs79270060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399522 | AAGTTCTTTAATGCC[A/G]ATTTGTGAGATTTTG | 10213 |
rs79323284 | snp | G/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344742 | CATTTAAAAAATTAA[G/T]TTATTTTTCTTTTTA | 10213 |
rs79405841 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386447 | CCATGGTTAAGCCTT[G/T]GTTACACTTTGATAA | 10213 |
rs79537952 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399575 | ATATACACTGCACCC[A/G]ATTTGTAGTCTTTGC | 10213 |
rs79541039 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385826 | AGTAGATCTTTTATC[C/T]TGAAAGCATTCTGGC | 10213 |
rs79699224 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366722 | AAGATTATAGGCATC[C/T]TGAGGGTAAGAACTA | 10213 |
rs79728503 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390557 | AATTCTGGTTGGTGA[G/T]ATTGCATGTCACTGG | 10213 |
rs79780609 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357562 | AAAGTAATTATTTCA[G/T]TTCCTTGTTTTACAA | 10213 |
rs79796151 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317260 | AGGATGAGTTAAGAT[C/G/T]GTGAAGTGGAAATTT | 10213 |
rs79875433 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321326 | GGTTATTTTATTTCC[C/T]TGATTGAAGAACAAG | 10213 |
rs79998242 | snp | G/T | 0.110872 | 0.20771 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401423 | CTCATTTGACAGAAC[G/T]TAGTTAAATGGACGC | 10213 |
rs80038263 | snp | A/G | | | missense | PSMD14 | GRCh38.p7 | 2:161371297 | TGGCAGTGGTTGTGG[A/G]TCCCATTCAGAGTGT | 10213 |
rs80128033 | snp | A/C | 0.444444 | 0.157135 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320923 | TAGAGATGGGGTTTC[A/C]CCATGTTGGCCAGAC | 10213 |
rs80218306 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336132 | CCACCTTTTATTCAT[A/T]TGGTCTCCACCTTTT | 10213 |
rs111249224 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161309806 | CTGTTGACTTTGGGA[A/G]TTTTTGGTTTTTTGT | 10213 |
rs111295449 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326808 | TTGCGCATAACCTAG[A/G]CACAGTCTCTCGCAT | 10213 |
rs111297957 | snp | A/G | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313810 | CAGTTCTGTATTTCA[A/G]ATACATTTCTAGTAG | 10213 |
rs111409374 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161308880 | AGAGAATCCTTGTTT[A/G]TGGCCTGTTTGTCTG | 10213 |
rs111421111 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319320 | CTAGTAATTATGATA[C/T]ATAGATGGATTAATA | 10213 |
rs111454693 | snp | A/C | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311773 | GTGCCTGCCATCACG[A/C]CCGGCTAGTTTTTAT | 10213 |
rs111455811 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405279 | TCTTTATACTCTCAT[C/G]CTGACTCTCCCTCTG | 10213 |
rs111525935 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368282 | CACATATACTGGTTC[C/T]TATGTCTTGTTCCCA | 10213 |
rs111562704 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161340341 | CGGCTGACCACCCTG[A/G]CGGAGCTGGTGAGCA | 10213 |
rs111610734 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346568 | ACATTGTGAGTCTTA[C/T]CTCGTGTGCTGGCTA | 10213 |
rs111613972 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331532 | CAAAGTGCTGGGATT[A/G]CAGGCGTGAGCCACC | 10213 |
rs111665577 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393398 | ATTTTTTTTGGCATA[C/T]TGTCCTTACCCCTGG | 10213 |
rs111669986 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331366 | CTCCCAGGTTCAAGC[A/G]GTTCTCCTGCCTCAG | 10213 |
rs111680555 | in-del | -/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367964 | TCATTTTTCTTTTCC[-/T]ATGCAAACTAACTCT | 10213 |
rs111778403 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322412 | ATTATTATTTTGAGT[C/T]AGAGACTTGCTTTGT | 10213 |
rs111794669 | snp | A/G | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389313 | TCCAGCTCAAGCTCC[A/G]CTCTCTACGCCAGAC | 10213 |
rs111923315 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376136 | ACTCTCTCTCATATA[G/T]AGAGAGAGGGCATAG | 10213 |
rs111932665 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366987 | GCTTCATTAGGTGAC[A/G]TGCAGAGGATGTTGT | 10213 |
rs111939812 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402912 | ATGAAAAATAACAAG[C/T]GTTGCCAAGGGTATG | 10213 |
rs111944314 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331518 | CTGCCTCGGCCTACC[-/A]AAGTGCTGGGATTAC | 10213 |
rs111991373 | snp | C/G | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390351 | TCTAGGCTGCCAGAG[C/G]ATCCTTTAGGTCCAC | 10213 |
rs112037128 | snp | A/C/G | 0.0131104 | 0.0800666 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161308311 | CCAGAGACAGGAGAC[A/C/G]CCGGGCCGCCCGCGC | 10213 |
rs112079806 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405479 | TGCTAGAAATTTTGC[G/T]GGAATTAACATATGA | 10213 |
rs112153463 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347275 | AGTTTCTGTTACTCT[A/G]TCTGTCTTGGACATA | 10213 |
rs112189917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323998 | GTGGAAACAGAGCCC[A/C]AGAGATGAGAATAGC | 10213 |
rs112225211 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362442 | AGTGGTTGTAACAGA[C/T]TTCTTTATATGACGA | 10213 |
rs112251817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352634 | CAGTTTCCCAAGTCT[A/G]TTTTTTCTTCCTTTT | 10213 |
rs112255012 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344650 | TCTTCTTTTTATTGT[A/G]TAGATCCATATTTTT | 10213 |
rs112262619 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347064 | CAGAGAGTCTACTGT[C/T]CTCTGCCTGGGTTTC | 10213 |
rs112312143 | in-del | -/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312145 | CAGTCTGAAAAGTAA[-/T]TTTTTTTTTTTTTTT | 10213 |
rs112335657 | snp | G/T | 0.161596 | 0.233848 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333926 | ATCACAGCTACTTGG[G/T]AGGCTGAGGCAGGAG | 10213 |
rs112473008 | in-del | -/AA | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401763 | TTAGGGCCACTTAAT[-/AA]ATCATGCATTTGACA | 10213 |
rs112586387 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313353 | TTTAATTAATTAATT[A/T]ATTTATTTATTTTTG | 10213 |
rs112591385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337601 | TTAATAGGCATTGCT[A/G]TCTTTGTATACTGAA | 10213 |
rs112777174 | snp | A/C | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360823 | TTACAGGCGTGAGCC[A/C]CCACGCCTGGCCTTC | 10213 |
rs112832377 | in-del | -/T | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394989 | CATTAAGTCGAAATG[-/T]TTTTTTTTTTTTGAA | 10213 |
rs112885099 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327510 | AGTCAGGTGCATAGC[A/G]GATACCCTTCCCCAA | 10213 |
rs112912339 | snp | A/G | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324616 | GTGTTGTAGTTTCAT[A/G]AAGATTTTCTTTCTT | 10213 |
rs112914246 | snp | A/C | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345468 | GGCTGGTCTCAAACT[A/C]CTGACCTCAAGCAAT | 10213 |
rs112923075 | snp | A/G | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331396 | GCCTCCTGAGTAGCT[A/G]GGACTACAGGCACAT | 10213 |
rs112934479 | in-del | -/AAATG | 0.5 | 0 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307214 | AAATAAAATAAAATA[-/AAATG]AAAAAGAAGTGAGGA | 10213 |
rs112940778 | snp | G/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409446 | TAATTAGACTGTTTT[G/T]TAAAGAATGTTGATT | 10213 |
rs112984811 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340111 | TTGCTTCTGCTATAG[C/T]AGAGTGGAGATTTGG | 10213 |
rs113026230 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307496 | TACCTATGAGTAAAA[C/T]AATCTTTGTGTTTTT | 10213 |
rs113034698 | snp | A/C | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354508 | AGCATTGTGCTTGGT[A/C]CTTGTTGCAGTGGAG | 10213 |
rs113040538 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342616 | TTGAGATGTTGTGTT[A/T]TGCTTTTTTTTTTTA | 10213 |
rs113098868 | in-del | -/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338173 | GCATCCCTAAGGTAG[-/T]TTTTTTCTTTTTTGC | 10213 |
rs113197261 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334707 | CTGCCACTTTTTCAT[A/G]CTCTTTAAGTATTTT | 10213 |
rs113225938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374686 | GGCACAGTGGGGACC[C/T]CCTGCTGAATGTTGT | 10213 |
rs113235674 | snp | A/C | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342070 | ATGCTTAGTTTAACA[A/C]AATATGTTTTGCATG | 10213 |
rs113269714 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393211 | ACTGTCTTTGTTTGC[C/T]TTTGAAGTGGTAGGG | 10213 |
rs113433607 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342844 | CCTTTGTTGAATTTC[C/T]AGCTATAACTTGTTT | 10213 |
rs113434098 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383006 | ACAAACATGGAGAAA[C/T]GCTTTCAGCTTATAC | 10213 |
rs113490237 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310983 | GCATCTGTAGATTCA[A/G]CCAACTACAAATTGA | 10213 |
rs113543924 | snp | A/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354180 | TTTGCCAATCTTAAA[A/T]GTTTATATTTTCTGG | 10213 |
rs113636393 | snp | A/G | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397503 | AGAGTTTATTTTTAA[A/G]GAAGCAATTAGAATG | 10213 |
rs113652012 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341526 | TGAAGACCAGAGTTT[C/T]TAATTTTGATAGTTT | 10213 |
rs113652522 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374172 | GCAGAATGCAAAATG[A/G]ATACCAGAGGTCATT | 10213 |
rs113680918 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346572 | TGTGAGTCTTATCTC[A/G]TGTGCTGGCTACTTT | 10213 |
rs113773284 | snp | A/G | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393766 | AACTTCTTATTTAAT[A/G]ATGGTCCTCAATTGA | 10213 |
rs113792082 | in-del | -/T | 0.47885 | 0.100637 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360367 | GAGCCTTTCATATTG[-/T]TTTTTTTTTTTTTTC | 10213 |
rs113858769 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329082 | CCACAGTATAGATCT[C/T]GCAGGGCCCTGTAGA | 10213 |
rs113919471 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336687 | TTCAAGTGATTCTCC[C/T]GCCTCAGCCTCCTGA | 10213 |
rs113962719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312925 | GCAAACTATGTGAGG[A/C]AGAAGGATCTGTGTT | 10213 |
rs113968401 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337428 | TAATCTTTACATTAA[C/G]CAGTACCACGTGGTA | 10213 |
rs113968767 | snp | C/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365623 | AGATTGCTCTGGATT[C/T]AGGAATAATTTTATG | 10213 |
rs114009378 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375639 | TCCACAGATATTAGA[A/G]TGTAAAATGAGTGCT | 10213 |
rs114033872 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316706 | GAAAAGTGGTGTGAT[G/T]TAGAATATGTATCAA | 10213 |
rs114058146 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394729 | ATACAAGTAATACAG[A/C]AGGTTAAGGGAAGAA | 10213 |
rs114103573 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363288 | CTGGCACCAAAGAGG[G/T]TGGGGACTGCTGCTC | 10213 |
rs114186763 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397537 | GACTAGGAATTAATG[G/T]TAAAGGCTAGAGCTC | 10213 |
rs114207008 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337012 | ATGAATCATTTACTT[C/T]GGAAGTAACTTATTC | 10213 |
rs114258420 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361799 | GTATCTCATTGACAA[A/C]TTTTGCTCAGTCTTT | 10213 |
rs114400544 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332642 | ATGAGGTTTCAAGTA[C/T]TACACTGCTTAATGC | 10213 |
rs114414258 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335631 | AGTGCTCTACTGATA[A/C/T]ACACTTAGGTTGTTT | 10213 |
rs114435389 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333674 | ATTTAGCATCATTCC[C/T]AGACCCTTCAACCTC | 10213 |
rs114447754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382881 | CCTACCAACCCATAC[A/G]TTAATTAATTCTTGG | 10213 |
rs114487257 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315397 | ATTTTGTAGTAATGT[A/G]AAACATTTTCTTTGT | 10213 |
rs114528650 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326762 | CAAAATCTATGGCTG[C/T]TCAAGTCCCTTAGAT | 10213 |
rs114553461 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325543 | TAAATGAAAAAATAA[C/T]ACTGTTTTCATGGAT | 10213 |
rs114603551 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368643 | CTTCTCACCTGTTTG[C/G]TTAGAAAAATATGCA | 10213 |
rs114610515 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330808 | TGGCTTAGGGACAAT[A/G]GAGTAAATAATAAAA | 10213 |
rs114745180 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348954 | TCCAGGTAGTTGTCA[C/T]GTGGCTCTTTCTTCC | 10213 |
rs114757979 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376468 | GAATGTTTCTGCAAG[C/T]TTTGATAAGAACAAG | 10213 |
rs114785989 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338240 | TAGAGCTATAAATTA[C/T]GAGAAATGAAGTTCT | 10213 |
rs114817319 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326156 | GATTCTTCTGCCTCA[C/G]CCTCCTGAGTATCAC | 10213 |
rs114823457 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405758 | TTTTAGCAGTTTGTG[C/T]TGTCTTATGTAAAAA | 10213 |
rs114832100 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316293 | AAGGGAGATCATTCT[A/G]TACTCTCAGAAAAAG | 10213 |
rs114854653 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347925 | GCAAACAGTGAGCTA[C/T]GGCTTGGGAAAGTTT | 10213 |
rs114859809 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393848 | TGAAAACTTAGGAAC[A/G]TCTAAGAATAAGTAC | 10213 |
rs114869326 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359901 | CCTTGTGATATATGT[C/T]GATGTAGATGTATAT | 10213 |
rs114886258 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361144 | ACTTTAATTTTTTAA[A/T]AAAACATGTAACTCT | 10213 |
rs114905174 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161356056 | AAAGGATTTTTTTTT[G/T]GAACATTTTTTTTTA | 10213 |
rs114914863 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335696 | ATATCTCATTGAAGA[C/T]GTTATTTCACATGCA | 10213 |
rs114946822 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335541 | TCCCATATCCATAGA[C/T]ATAAAGCTGCATGTT | 10213 |
rs114962177 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348131 | CAGAATCTGTTAACA[A/G]TGAAGATTTGACTAA | 10213 |
rs114974659 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343317 | ATATGGAATCATTCA[A/G]TATTTGTCATTTTGT | 10213 |
rs114981466 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360931 | TTTTTAATTTGCTTG[A/T]GTACTGACTTCTTGT | 10213 |
rs114992435 | snp | C/G/T | 0.00676609 | 0.0577691 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343921 | CTGCATCCATGGATT[C/G/T]AACCAACGTTTACAT | 10213 |
rs115041848 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351933 | TGTGCCTGAGAGAGC[A/G]GAACCAGAAATATTT | 10213 |
rs115070554 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342631 | TTGCTTTTTTTTTTT[A/T]AAATCCAGTCATAGT | 10213 |
rs115090820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407356 | TGTCTAGATTTGGCA[C/T]GTTATTAACTTTTTC | 10213 |
rs115136953 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335609 | ACAAACCATGATTTA[C/T]TTAATTAGTGCTCTA | 10213 |
rs115175467 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384802 | TATTGTAATATCTTT[A/G]CCATGAATTTAGGAC | 10213 |
rs115185856 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376986 | TGTCAGCATAGAGTC[A/G]TTTATTAAATGACTG | 10213 |
rs115202258 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312523 | TAAAGTGAGAAAGAA[A/G]AAGTGGAAAGTAATC | 10213 |
rs115209301 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410180 | AATGGAATTAAACCA[A/G]TATCTTTTTTTCTCC | 10213 |
rs115211588 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346697 | TAGTTAAGACTGGGG[C/G]AGTACCTTGTTTAGG | 10213 |
rs115217891 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407609 | AATGCAGCCAAACTT[C/T]CCAGTTTATGGGGAA | 10213 |
rs115224838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349012 | TGGCCTCTCACTCCC[A/G]GAGAGGCATCTTTCT | 10213 |
rs115264567 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319728 | ATCAGTGACTTCATC[G/T]TTCTTCAAAGTAATC | 10213 |
rs115303359 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332800 | GCTCTGGCCTGTGCT[C/G]GGATTACACCAGAGT | 10213 |
rs115329230 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319497 | TCTATCTGCTTTCAG[A/G]TCAAGAATTTGTGCC | 10213 |
rs115383457 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334730 | AGTATTTTTCTTCTG[A/G/T]TGTGTTTTCTTTTTT | 10213 |
rs115428242 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401373 | GTTAGCACCCATAAC[A/C]CTCATCCCCATTTGT | 10213 |
rs115432269 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327722 | AATCTGCAACACCAC[A/G]TAGTTCATTCAGCAG | 10213 |
rs115443333 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324767 | AAGAGATTAAAGGCA[A/G]AGTCATCAATTACAT | 10213 |
rs115444205 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325535 | GACTGGAATAAATGA[A/C]AAAATAATACTGTTT | 10213 |
rs115502544 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379359 | GAGTGTAGAAACACC[A/G]ATCATGCAGGAGTAG | 10213 |
rs115533501 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161328831 | CTTCAACTTTATAAT[A/G]TTCTCTCTTTAGTAC | 10213 |
rs115539479 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392080 | GCATTCTCATTTGTT[G/T]CTATTTTAGGATTAT | 10213 |
rs115591556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347144 | GTAAGGCTCACCTCA[C/T]TTGTTTCCCAAATTT | 10213 |
rs115601991 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357759 | TTATTTTATAGTGGC[A/G]TTGTATGAAAGACGA | 10213 |
rs115644261 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316797 | TAATTTGTTAAATAT[G/T]TTTCCTCTTTGCTGT | 10213 |
rs115644511 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359002 | CTGGAGATAGGGCCT[C/T]GTTGTCCAGGCTGGA | 10213 |
rs115647511 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407343 | TGAGCATATTCTCTG[C/T]CTAGATTTGGCATGT | 10213 |
rs115718046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343421 | TTGAATAATATTCCA[C/T]TGTATGTATGCATAC | 10213 |
rs115739806 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374835 | CATAAAACTAGCATA[C/T]AACTTAATTAGGATA | 10213 |
rs115774585 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342851 | TGAATTTCTAGCTAT[A/G]ACTTGTTTTGTTAGT | 10213 |
rs115781069 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381491 | TTTGTGTATTTTTTT[A/T]AAAACAGCTTTGTAT | 10213 |
rs115837023 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332061 | AATTAATACAACTTA[A/C]ATAGTCTTGTAATTT | 10213 |
rs115846335 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326390 | ATCCAAATTAAACAA[C/T]AACAACAACAACAAA | 10213 |
rs115857418 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346017 | CCACCTCAGTCTCCC[C/G]ACTACAGTCATGTGC | 10213 |
rs115910799 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313203 | TCATAGTACTTGACT[C/T]TCATGTACCAGGCAA | 10213 |
rs115942505 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409129 | AGTGAAAATAATTTA[C/T]TAGGAACAAATTAGG | 10213 |
rs115945132 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333466 | CCTGGCACAGGTTTC[A/G]GACCTACCAACTCAC | 10213 |
rs115957273 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369048 | TTAACCAAAGGTTTA[G/T]ATTTAAATCTTAGAC | 10213 |
rs115964825 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324814 | CAACCTTCCAGGCAT[A/G]TAACAGGATTATATT | 10213 |
rs115971232 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359798 | AAAAGTAGACTTGGG[C/T]ATCTGAAAATGGGAT | 10213 |
rs115971339 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316965 | TGAACACAGCTGGGA[A/G]TCAGTTTTGGCCTAG | 10213 |
rs116062779 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356338 | TAGTTGTTTAATACA[A/C]AATTAAAGTATTAAA | 10213 |
rs116071344 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325850 | AATACATCCATCAAT[A/G]TATGGGAACTTGGTT | 10213 |
rs116101550 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403554 | ATTTTTAAAAATGCA[A/G]ATTGGTTCATGTCAC | 10213 |
rs116122913 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326592 | AGAGACTCCAACAGA[G/T]GTTTGTACACCAATA | 10213 |
rs116123485 | snp | A/T | 0.0607341 | 0.163335 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315611 | TCACTATTGCATTAT[A/T]TTCCATATTCTTGTC | 10213 |
rs116187182 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404965 | GAAATCTCTTCATTT[C/T]CTCTCATTTGAAATG | 10213 |
rs116188096 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317846 | TCTTAAGCATACACT[C/T]AGGAAGAAGAGGAAT | 10213 |
rs116232910 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387346 | TTATGTTAGCAGGAT[C/G]TTTAACTCTGGGATC | 10213 |
rs116255458 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356791 | TTTACAAATTTTTGA[A/C]ATGTTTAATGTCATT | 10213 |
rs116288495 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400950 | AAACATACACTAATC[A/T]ACTATAAAATAAAAA | 10213 |
rs116328716 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350324 | TAGTAAAAATACTTA[C/T]TTATCTGAAATTCAA | 10213 |
rs116333687 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329189 | TAAAGAACTTGGACA[C/T]TCTGAAGATGAAGCT | 10213 |
rs116357718 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327015 | GGGCTGATTGTACAT[A/G]CAATGGAATATTATT | 10213 |
rs116384042 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404629 | AACCTTTTCATGACA[A/G]AGTATGGCGCTGATG | 10213 |
rs116438683 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380029 | TCCACAGCAGGTTCT[A/G]TTGAAAGATCTGAGC | 10213 |
rs116483066 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400633 | ATCATGGTTCACTGT[A/G]GCTTCCACCTCTTGG | 10213 |
rs116507976 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389257 | TGTAGGGTTGTGCAA[A/G]TAGTGAGTGCATCGC | 10213 |
rs116572700 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326584 | TTGAAAGCAGAGACT[A/C]CAACAGATGTTTGTA | 10213 |
rs116577030 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319636 | ATGTATTGTTTTATG[A/T]CCAAATATTAGAAAT | 10213 |
rs116594690 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318502 | CAGGCACTTTTTCTA[C/T]ATTCAGGTACTTTAT | 10213 |
rs116653935 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348560 | TGAAAAATGAATAAT[C/T]CTCACATAGTTCATA | 10213 |
rs116692862 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307321 | ACATTTCATGGTTTC[C/T]ACAGTGGGGAGAGAT | 10213 |
rs116730965 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352621 | ACTATCTGCCATCCA[G/T]TTTCCCAAGTCTATT | 10213 |
rs116747328 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368158 | TCGGCTTAAACTGGT[A/G]TAAAATACTGGATTT | 10213 |
rs116754729 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347729 | AAGGGACGATTGATT[C/T]ATTTTCATCTAAAAA | 10213 |
rs116756201 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335468 | AGCTGCATGTGGCCA[G/T]TGGCCACTATATTGG | 10213 |
rs116791878 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392005 | TAGATTCTGATCCCA[C/T]TTTATACCAGTTTTC | 10213 |
rs116809341 | snp | C/T | 0.00616327 | 0.0551693 | intron-variant | PSMD14 | GRCh38.p7 | 2:161411290 | TCTCTTTCCTCATTT[C/T]TGTTCTTTTAGGACC | 10213 |
rs116837966 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374604 | ATAGTTTATAAGGTC[C/T]GCTTGCAGCATTTAG | 10213 |
rs116860929 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363573 | CCTATATTTAGGTGA[A/C]TTTCTTTTTGAATCA | 10213 |
rs116897934 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384087 | TATAAAAAGAAAAAA[A/G]TTTTCACAAACTATT | 10213 |
rs116988788 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337463 | TAGCACCATTCACAA[C/G]GGAAAATGGGTCATA | 10213 |
rs116990879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407004 | TAACTGTTTTGTACA[C/T]GGATTGGTATTTTGA | 10213 |
rs117493522 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358772 | ACATGGTGAAACCCC[A/G]TCTCCACCAAAGATA | 10213 |
rs117684119 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407423 | ATGATGTGTTGTAAA[C/T]AAGTATCCTTTGATA | 10213 |
rs117995630 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316918 | GGAGTCTGTGTAAAG[A/T]CATCAGAAACAACAC | 10213 |
rs118087283 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359443 | AAGTCTCAAATGCTT[C/T]GTGTAACTTAGATTT | 10213 |
rs137859411 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354486 | TTTTTTATAACAAAG[A/G]TAGTCGAGCATTGTG | 10213 |
rs137935816 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161411775 | TAACATTTGACAGTG[A/G]TCTAGAAATCTCACA | 10213 |
rs137993921 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362075 | TAATTTTAATTAAAA[A/C]AATTTTTTTGAGACA | 10213 |
rs138003760 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349777 | CTGTGAGCCAGACGA[A/C/G]CAGGGTGGGGTTGGA | 10213 |
rs138061422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368470 | CTCCATACAAATTAC[C/T]TGTATAGAATACATT | 10213 |
rs138127532 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318159 | TTTCCTTAGTGAAAA[A/C]GGTGTATATATCTCT | 10213 |
rs138265971 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383214 | CAAAATTAAAATGTA[A/G]ACTATATTGCCATGT | 10213 |
rs138328565 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324199 | GTATCAGGTATTATA[C/T]ACTATAACGAATTCC | 10213 |
rs138340137 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161341863 | AAAAAAATTAAAATT[-/A]AAAAAAATATATATG | 10213 |
rs138387393 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375131 | GGTCAGCTTATCTGC[A/G]GGTATTTCTTAAGTG | 10213 |
rs138393944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394438 | TAAACTGAGGATCAG[A/G]AAGATTGACACAAGG | 10213 |
rs138399912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348170 | CCAGCAAATCTTCTC[C/G]TAATTACATTCCCTA | 10213 |
rs138442910 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401355 | GATTTTCACCTGTGA[C/G/T]GGGTTAGCACCCATA | 10213 |
rs138541092 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396322 | GTTGAAGAGATGTAT[A/G]CACTCCCATGTTTAT | 10213 |
rs138550660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409809 | ACCTTCTAAGTATTA[C/T]AGTTTAAAAACAAGT | 10213 |
rs138609145 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355307 | TTAGGTATGTTTTCT[A/G]ATGTTTAATTCTTAC | 10213 |
rs138635471 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311178 | GCCGGGCATGGGGGC[A/G]TGTGCCTGTAATCCC | 10213 |
rs138690532 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316659 | ATTTTTAACAGATGT[C/T]AAATTATGAATGTGA | 10213 |
rs138697606 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161369088 | CTTGTATCTGTCTTT[C/T]TATATTAGGCTACAT | 10213 |
rs138755100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368877 | CATTTAAAATAGAAT[A/G]TTTGCTACAGAATGC | 10213 |
rs138794329 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394031 | GCTGGAGTGTAGTGG[C/T]GTGACCTCAGCTCAC | 10213 |
rs138919923 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338283 | GTGTGTGCACATGTG[C/T]GTGAGCATGTATTCA | 10213 |
rs138920239 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408783 | GGTGATTATCCTGCA[C/G]TGGGAATAGAGGATT | 10213 |
rs138982469 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332115 | GCTTGCTTTTTAAAA[C/T]TTTTGGGAAATTAAA | 10213 |
rs139010832 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402143 | CTCTTCGCATTGCCA[A/G]TTCCACTGCCTTACC | 10213 |
rs139029231 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161356061 | ATTTTTTTTTGGAAC[-/A]TTTTTTTTTAACTCT | 10213 |
rs139064774 | snp | G/T | 0.0700422 | 0.173537 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334057 | AAACAAAAAGGCCAG[G/T]CCTGGTGGCTCACAC | 10213 |
rs139129574 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324285 | CAAGCAATCATGTTT[C/T]AAGTGCCTAGTACAC | 10213 |
rs139178879 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161356058 | AGGATTTTTTTTTGG[A/G]ACATTTTTTTTTAAC | 10213 |
rs139342607 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325748 | TGCTCTACCAGATTT[C/T]GAAACATATTTTAAT | 10213 |
rs139373516 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307122 | GTTGCAGTGAGCCCA[C/G]ATGGCGCCACTGCAC | 10213 |
rs139414192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386925 | AATCAATATTAATAA[C/T]GTGTTTTTTCTATAC | 10213 |
rs139418358 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356655 | TGTTATAAAGCATAT[A/C]TTTTAACAGACTTTT | 10213 |
rs139476612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357772 | GCATTGTATGAAAGA[C/T]GAGACTATTTTATGT | 10213 |
rs139519819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339664 | CTAGGAGGGAGTCAA[C/T]GACCTATTGTATCAA | 10213 |
rs139543802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363886 | AGTGGGTGTGTGTTA[C/T]AGGGTGCTCTTTTAG | 10213 |
rs139623338 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352026 | AATTTGTAAACCTCT[A/G]TATCTCACTAAATTG | 10213 |
rs139626504 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340464 | TGAACTCTGCTTTTA[A/T]AATGTTCGTTTTATC | 10213 |
rs139695890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345687 | GAACTTCATGTGTCC[A/G]AAGGCCTGTTATTTT | 10213 |
rs139792532 | in-del | -/AT | 0.0126979 | 0.078662 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314637 | ATGGAATCACATAAC[-/AT]GTGAGCTTTTGTGCC | 10213 |
rs139796199 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387664 | CCATTCTGCAAGTGT[A/G]TATTTTATAGATGGT | 10213 |
rs139836287 | in-del | -/A | 0.0244538 | 0.107838 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409163 | CTTGTATCCTGAATT[-/A]ATTTTTTAAGTATTA | 10213 |
rs139845400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375948 | AGATATCTAGAAGGT[C/T]GTGTCTTTTCTTTCA | 10213 |
rs139868322 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379400 | CTAGGCATATTCAGT[C/G]ATTTTTAAAAGAGAG | 10213 |
rs140048225 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351729 | TATGTCTACATGGGT[C/T]GTCTGGGTGCTCTGT | 10213 |
rs140074060 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373581 | AAAATGAAGAATAGT[A/G]TAAGAGTCTCCCTCT | 10213 |
rs140114478 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370247 | TACCTCAAAGTTATA[A/G]ATGTTTATCAATGTC | 10213 |
rs140139657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315146 | TTTATCCCCCGGGGA[C/T]GTTTGGTAAAGCTTG | 10213 |
rs140177240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333683 | CATTCCCAGACCCTT[C/T]AACCTCCTCAAGTGG | 10213 |
rs140281821 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381183 | AAATTATTTCAGTTC[A/G]TCACTTATGTTTACC | 10213 |
rs140294491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161328322 | TGAATGAACTAGGTT[A/C]TATATACCAATATGC | 10213 |
rs140367301 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322064 | TCTTTATGTTGATCA[A/G]CCCTCATCTGCAAGC | 10213 |
rs140439564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337041 | TCAAAGTCATTTAAA[G/T]AAAAATTAATCTTTT | 10213 |
rs140440460 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161361465 | ACACGGATAGATTTT[-/T]TTTTTTCACATACAT | 10213 |
rs140489394 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397230 | TAAGAGAAGATTTGA[A/G]ATGGAGAGTGTGTTT | 10213 |
rs140510496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400419 | ACTCCTGATTACAAC[C/T]GGCCCTGGAACTATA | 10213 |
rs140616188 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409000 | TTTCCTGTCCACTCT[A/G]TGTTTTTCTTCTGTC | 10213 |
rs140684833 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347135 | TAAGCTAGGGTAAGG[C/G/T]TCACCTCATTTGTTT | 10213 |
rs140744722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367179 | ACATATACACACTGT[C/G]GTAACAAATGTGGCT | 10213 |
rs140767697 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320765 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAATGC | 10213 |
rs140820166 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330283 | TATGACATCTGATAC[C/T]ATTTTTGGTAGAAAG | 10213 |
rs140884005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314101 | AACATTTATATTTTT[A/G]GATTTATAGGCACCA | 10213 |
rs140904684 | snp | A/C | 0.0722614 | 0.17581 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316000 | GTGCCTGCCACCACG[A/C]CTGGCTAATTTTTTT | 10213 |
rs140948098 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319524 | TGCCTCTTGTGAGTT[C/T]GACACTTTCGATCTG | 10213 |
rs140984065 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368673 | ATGTATTTTTCCAAG[C/T]GATATTTCTTCTTTG | 10213 |
rs140992526 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342334 | CTACTTTGTTGAGAC[A/T]TTTTTTTTTTATCAG | 10213 |
rs141050961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373853 | TTTGATTTTCTTTTA[C/T]GATGACTTGATTATA | 10213 |
rs141108977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347593 | GATTAACAGAAAGTA[A/C]TATTCTTAGCATTCA | 10213 |
rs141172447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353864 | GTCTCTCTGTGTGTA[A/G]TATTTCATACATGGC | 10213 |
rs141182118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360281 | TGCAGCCTTGACCTG[A/G]GCTCAAGTGATCCTC | 10213 |
rs141306945 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368885 | ATAGAATATTTGCTA[C/T]AGAATGCAATATATT | 10213 |
rs141371104 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407970 | AATTCTCAATAAAGA[A/G]GTTTTATATTGGTGC | 10213 |
rs141403118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374877 | TTATTAAAAAGCATT[A/G]CTGCTTTAGAGAACT | 10213 |
rs141437302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317460 | AATTTTACCTTTGCA[C/G]GGTGGAATAGACTGG | 10213 |
rs141439805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336315 | TAAGCAGAGTCACCA[C/T]ATTAATAAAACACTG | 10213 |
rs141518366 | in-del | -/T | 0.0310518 | 0.120672 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372631 | TTTCAATTTATTTAC[-/T]TTTTTTTAACTATAT | 10213 |
rs141518812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385638 | TGCTATAAGTAGTCT[C/T]TTTAAGTTCTAATTC | 10213 |
rs141527660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396425 | TGGTGTATAGATATA[C/T]ATACAATGGAATACT | 10213 |
rs141588450 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382643 | GGCCTTCAGCATGGA[A/G]AGGAATTTTTCAAAG | 10213 |
rs141626882 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339385 | TGCATTTTCTGGATG[A/C]CTGATGATGGTGAGC | 10213 |
rs141699977 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403848 | CCATACCACCAAATG[A/C]GTGCTATTTACTCCT | 10213 |
rs141704526 | in-del | -/A | 0.311369 | 0.242351 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327878 | AGATTAGTTAAAAAA[-/A]CAAACAAACCTGTGG | 10213 |
rs141731108 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317131 | AAAATATACAGGATT[C/T]CCCCCGCCCCGTTTT | 10213 |
rs141863521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359498 | TTTTTTTAAGGCAAA[G/T]ATTTTTTTTTTAATT | 10213 |
rs141935385 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333140 | ATTTGTTTAATAATA[A/G]CATAGAAATATAAAT | 10213 |
rs141944813 | snp | A/C/G | 0.0158469 | 0.0875917 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360107 | TTCTCTGATAGGACT[A/C/G]TGTGGCTCATGGAAT | 10213 |
rs142206787 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333867 | GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAT | 10213 |
rs142228860 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351257 | TAGTGTGTCATTGTT[G/T]CTGGTGAAGGTGGTC | 10213 |
rs142268352 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338422 | GAGTACTATTTTTGC[A/C]ATTGATAACCTGTAT | 10213 |
rs142276285 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161398767 | TTTCTTTTATATGCT[C/T]ACATATGAAATATGT | 10213 |
rs142296529 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391267 | ATTTAAATTCGAATT[C/T]TTGACCTCTTTCAGT | 10213 |
rs142302580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365112 | CTCCGTCTAAAAAAA[A/C]CCAAAAATAAAACAG | 10213 |
rs142329793 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392040 | TTGATTAGTTTTTAA[C/T]ATTACCTGACGTTTT | 10213 |
rs142359841 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306484 | CATTAGGTTGGTACC[A/G]AAGTAATTTCGTTGA | 10213 |
rs142369120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161398637 | AGAATAGCATAGAAA[C/T]AAAAATTTGCCTTTT | 10213 |
rs142369305 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330922 | CTGTGGTAATTTTCT[A/G]TTCCCTAGTGTTGTA | 10213 |
rs142538651 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329389 | CACTGGCATAGTAGT[A/G]TGCAAATGAGCAGAC | 10213 |
rs142612651 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388863 | GCATAGAGGTAAAAT[A/C]ATAAGTCAGTTGGTC | 10213 |
rs142616951 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357385 | TGCCTGTGGCTCAGC[A/T]TTTTACCCTACAGTT | 10213 |
rs142676427 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362241 | TGGTTAAAGTTGTTC[A/G]AAAAACTAATTTATG | 10213 |
rs142758439 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343858 | TGTCTTTGAGTCTCT[C/G]CTTTTAGTTCTTTTG | 10213 |
rs142887426 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407279 | CAATTTCCCAGTTAG[G/T]AAATACTTTTATAAC | 10213 |
rs142887430 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357997 | CTGATAATTTTAGAA[C/T]TATGCTCTTGATTAA | 10213 |
rs142939378 | in-del | -/T | 0.0547245 | 0.156101 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307619 | CATCACCATTCTCGA[-/T]TTAGGAATGCTTTAA | 10213 |
rs142949361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319917 | TTTCAGTTGTTTTTC[A/G]TTTACTTTTGTTAGT | 10213 |
rs143015561 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387182 | CAGTTTTAAGACAAT[G/T]TCAATACTAAAACAC | 10213 |
rs143065223 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324697 | CTTGTGAGGTAATTT[A/G]ATCTGTGTTTTTGAA | 10213 |
rs143080524 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394786 | GACTATTTTAGGTAT[A/G]TTGTTGTTAGGGAAG | 10213 |
rs143094436 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360169 | AGCTTTTTTCCACCC[C/T]GTAACATATATATAT | 10213 |
rs143164022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327666 | ACAGAAACAAACTTA[C/T]AAGACAAGCAAAGAT | 10213 |
rs143166605 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324087 | TGGAAATAGTCAATA[G/T]AAGCTTGAAAGTAGA | 10213 |
rs143269926 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396598 | ACTCATAGAAGTAGA[G/T]AGTAGAATTGTGGTT | 10213 |
rs143281385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384778 | CTGTACACACAAAAA[G/T]AATATACTTATTGTA | 10213 |
rs143307664 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320794 | GCAATGGCATGATCT[C/T]GGTTCACTGTACCCT | 10213 |
rs143309420 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388059 | TTTATTTTAGTAACT[A/G]AATTTTTTAAACTAT | 10213 |
rs143406538 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352888 | CAGCTTTTATGACTG[C/T]TTAGTGGCTCTAACA | 10213 |
rs143482601 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349813 | CAGCAGGGCTTGCAA[G/T]GTATGGTCTAAACTG | 10213 |
rs143511924 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309649 | GAGGTTAAGATATAT[A/G]GTGGTTCTGAATTAA | 10213 |
rs143549510 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354872 | CCCTGCTATTACATC[A/G]CTTCACCCCACTGCC | 10213 |
rs143586687 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374483 | TTGTACAGTACTATA[A/G]ATGTTTTAAAATGAT | 10213 |
rs143652310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341963 | ACAAACATATTCTCT[G/T]TTCTTCCAGAAGTTT | 10213 |
rs143692985 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332861 | AATTTTGGTTGGGGA[G/T]CTGACTGGCACAGGC | 10213 |
rs143726025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347005 | ACTCTGTCCAGATTA[C/T]GAGTTGTTTTGGTCT | 10213 |
rs143766680 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394359 | TTTAAATTATAGATG[C/G]AATACCAGAATTTGA | 10213 |
rs143811798 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324234 | CGAACAAGAATATCA[A/G]TGCCTAATCCAGAGC | 10213 |
rs143873542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343343 | TTTGTGACTGGCCTA[A/G]CATAATGTCATTAAG | 10213 |
rs143888382 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375522 | GCTGAGCTTTGAGGG[A/G]TAGGCAGGACATCAC | 10213 |
rs143922143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318668 | CAGCTTCTTGAATTA[A/G]TATGTGGTGTTAATT | 10213 |
rs143922263 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383711 | GAAATCTTGAAATGG[A/G]CCAAAATGATGCTTT | 10213 |
rs143982740 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379259 | TTGATATCAGACTAG[C/T]GACCCATAGGTGATA | 10213 |
rs144020352 | in-del | -/TT | 0.0402882 | 0.136092 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347845 | TAATCTTTACAACTC[-/TT]TGCAGTTTGGTTATT | 10213 |
rs144042472 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350630 | AGCAGGAAGGAGAGG[A/C]GATCTCAGATCATTT | 10213 |
rs144052771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396976 | GGGATTACAGGCGCC[C/T]GCTGCAACACCCAGC | 10213 |
rs144057356 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373771 | TTTATAAATTCCAAT[A/G]TTTCTGTCTTTGAGA | 10213 |
rs144261865 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352100 | GGTGATTGGCTCAAG[A/T]CCTCTGAAATTCCTA | 10213 |
rs144262443 | in-del | -/A | 0.135825 | 0.222405 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368852 | TATGTATATTAAAAA[-/A]TAAGCATTTAAAATA | 10213 |
rs144308107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364248 | GTGTGTCCCTCTGCT[A/G]ATGTGCTCCTCTCTC | 10213 |
rs144382914 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327400 | TTTACTACAAAAAAG[A/C]CATTTAAAAGTTCAG | 10213 |
rs144396218 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404392 | GTAACTTTATTAAGT[G/T]GCCAATCATAAGCAC | 10213 |
rs144444193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402361 | GAAAATAGAAAGGCA[C/T]GTGTGGTGGCACATG | 10213 |
rs144546047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397579 | ATCATAGTTAAGATT[A/G]TTGTTGGTTATTACA | 10213 |
rs144646755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356019 | TCTCTTCTGAATAAT[A/G]TAGTCATTGAAACTG | 10213 |
rs144647588 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161316481 | GGAAGTTGTACCTGC[C/T]AGAATTAGCAAGAGC | 10213 |
rs144758618 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313828 | ACATTTCTAGTAGGC[A/G]CTAGCTGATTACTTC | 10213 |
rs144789766 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373968 | ATAGGCCCTGTTACC[A/G]TTACATGTTATTAGT | 10213 |
rs144792803 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386017 | AAAATTTTCTTCTTT[-/A]AAAAACCCACCTTTA | 10213 |
rs144817597 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319616 | CTAAGACTTTTATAT[A/C]TGCAATGTATTGTTT | 10213 |
rs144826424 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376597 | TCTAGGAATACTCTT[C/T]TGATTGGCCTACTTT | 10213 |
rs144860771 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319671 | TTATAGTCCCTTTTA[A/C]AATCTCTTTAGTTTC | 10213 |
rs144870224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315644 | TTTAGTGTTTTTGGA[A/G]TAGTTGATTAAGAAA | 10213 |
rs144928030 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368818 | GGAGAACAAATTACA[A/G]TTTTAAGTACTGTAA | 10213 |
rs144935719 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334894 | TTCTATCTGTTCCCT[C/T]AATTCCTCAGAAACA | 10213 |
rs144959209 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314114 | TTAGATTTATAGGCA[C/G]CATTTAGAATTAGTC | 10213 |
rs145089858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382560 | TGACCTCTGAAAAGT[A/C]TCAAGGCACTTGTAC | 10213 |
rs145114774 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408067 | TGCCAGAAAGTTATG[A/G]TCATACATAGAAGAG | 10213 |
rs145114876 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337666 | CTTAGTTTATGGTGA[C/T]GGTCCCATGGCTGCC | 10213 |
rs145188155 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402090 | TCACATCTACTCAAT[C/T]AGTAAACCATTCTGA | 10213 |
rs145206571 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346607 | TCTTAGAAATATTCT[G/T]GATATTTGTTATGGG | 10213 |
rs145235192 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345866 | TGTTTCATTTTTCTG[A/T]TGCTACATCTTCAAG | 10213 |
rs145309797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368103 | TCTTATAGGTCTACA[A/G]ACTGAATGATGCTAA | 10213 |
rs145316329 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340496 | AAGGTGTGCAGGGTG[A/T]GTGGATAGCAAGTTT | 10213 |
rs145406439 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313952 | GGCATTAAGTATATT[C/T]ACAGTGTTATGTAAC | 10213 |
rs145436627 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367362 | CAAATAAAAGGATAC[C/T]TGACATGTTTTGCAA | 10213 |
rs145468711 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161308670 | GCCGCCGCCAGCCCC[A/G]TGCTTTCCTGAGTCA | 10213 |
rs145501397 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388558 | CCTTCTGCAACTCAG[A/T]TCTCCACTCTAGAGG | 10213 |
rs145552698 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307168 | AAAGCAAGACCCTAA[C/T]TCAAAAATGCATTAA | 10213 |
rs145552809 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370838 | GAAAATCCAACTCCC[A/G]GAGCTAAGGAGTTAA | 10213 |
rs145698112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366603 | TAAGCAAAACACGAC[C/T]TGGCAATTATAAGTC | 10213 |
rs145718824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406418 | AAAAGCAAAATTTGA[C/T]GCCAAATCACAGAAG | 10213 |
rs145854516 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388297 | ATATAAGTTATAAAA[-/C]CAATTGCACTAGAAA | 10213 |
rs145933362 | in-del | -/A | 0.0182019 | 0.0936463 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395710 | CTCATTAATGGGTTG[-/A]AAAACCTACAATTTT | 10213 |
rs145946577 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161387209 | ACACACAAATGAGAC[C/T]AAGCCAACAAGTGAC | 10213 |
rs146025124 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363419 | ATAATACTTTTACCC[A/T]TGTTTCTCCTAGTGT | 10213 |
rs146081987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391627 | AGTAGGGTCTTGCTC[C/T]GTCTCCCAGACTAGA | 10213 |
rs146149534 | snp | A/T | 2.68568e-05 | 0.00366438 | missense | PSMD14 | GRCh38.p7 | 2:161395151 | GTGAACATTGTAAAC[A/T]CAATGAATCAGTGGT | 10213 |
rs146308788 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357540 | AGTATTGAGGATTTA[C/T]ATAGCAAAAGTAATT | 10213 |
rs146389174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338773 | AACATCCATCATTCT[C/T]AGAATTTACATATGC | 10213 |
rs146411153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379373 | CGATCATGCAGGAGT[A/G]GTATCAAGATTCTAG | 10213 |
rs146452493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373830 | TAATCTCAATTCATT[C/T]ACAATAGTTTGATTT | 10213 |
rs146454429 | in-del | -/TTTG | 0.0193772 | 0.0965046 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348928 | TGGTTAGAAAAAACA[-/TTTG]TTCCTACTCCAGGTA | 10213 |
rs146576039 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407629 | TTTATGGGGAATGTC[C/T]GATGATTACATTTCC | 10213 |
rs146688992 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321661 | ATTTGGAGGTCCTCA[C/T]AACCTCCTCAGGTTT | 10213 |
rs146707797 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327914 | GAATTAAGTGTTAAT[A/G]AAAATTGGGGAAGCA | 10213 |
rs146766349 | in-del | -/ACTC | 0.0146672 | 0.084371 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403203 | TTACAACATACTATT[-/ACTC]AGTCATAAAAAGGAA | 10213 |
rs146774175 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351997 | TTAGTCTCTCTACTT[C/T]ATATATCTATGATAA | 10213 |
rs146896366 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161308356 | GCTCCTCCTGGACAT[C/T]CGCTTGACTCTCCGT | 10213 |
rs146933917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354171 | AGTTATGTTTTTGCC[A/G]ATCTTAAATGTTTAT | 10213 |
rs147107236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359603 | CCCACTGTGCCCATC[C/T]AGACTTCAGGAAATA | 10213 |
rs147160690 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404219 | CAGCCTAATTATTAC[G/T]TTTTAATTTCCTGGT | 10213 |
rs147243946 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365468 | TGGCAGAAATAGTTT[C/T]TGGATTCTTTCAGTA | 10213 |
rs147268172 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319390 | TTTATAATCTTTTTA[A/C]AAAATAAATAAGCTT | 10213 |
rs147284582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324258 | CCAGAGCCTTACATT[A/G]TAATAGACACACAAG | 10213 |
rs147288033 | snp | G/T | 0.000919979 | 0.0214276 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161371226 | CTTTGGTTGTTGGCT[G/T]TCTGGTGTGGATATC | 10213 |
rs147304927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375746 | AAGAAAGTTAGGGAA[C/T]GTGGCCAGGTACCAT | 10213 |
rs147373813 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345004 | TGTTTGCTTCAAGAG[A/T]TTTATTGTTTTATCT | 10213 |
rs147391520 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349421 | GTGAGTCAAAAATAA[A/C]AGCTAAAACTGCATT | 10213 |
rs147393558 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404431 | ACTAATATTAACATA[A/C]TATAAACTAAAATTT | 10213 |
rs147479451 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369972 | TATGAGGTTTATAAT[C/T]GAATGACTTGAGTAG | 10213 |
rs147494686 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344133 | GGGGTGGGGAGCGGT[-/G]GGGGGAGGTCCTGAA | 10213 |
rs147495963 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375113 | GATGTTTATCTAACT[G/T]CAGGTCAGCTTATCT | 10213 |
rs147542339 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389157 | AGTACAGTTAGTCTC[-/A]AAAATATAGGGCCTA | 10213 |
rs147676184 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391977 | AGTTTTAGGGTTTTC[A/G]GATAATTTGTACTAG | 10213 |
rs147690168 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365105 | AGCGAGACTCCGTCT[-/A]AAAAAAACCAAAAAT | 10213 |
rs147699785 | in-del | -/GTTG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389886 | TTTTCTTTCTTTTTT[-/GTTG]TTTTTTTTTTTTTTT | 10213 |
rs147725026 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314006 | ATTTTTTCATCCTCC[C/T]AATTGCAATATTTTT | 10213 |
rs147755986 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307694 | TGGCAAACAAGCTGC[C/T]TTAAACAGAGACTGT | 10213 |
rs147812990 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336255 | ATAACTTTTATATCA[A/C]CTGGCAAAATTGTGG | 10213 |
rs147829125 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340276 | ATGGCATCTCACCCC[C/T]GACAACCAAGCCAGC | 10213 |
rs147848684 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161398555 | TTTTTTTTAATTTTG[A/G]TAATGTTTGATTACA | 10213 |
rs147919699 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359163 | AATTTGTGGAGATGC[A/G]GTCTTACTATGTTGC | 10213 |
rs147971587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403633 | AATGAGGTCCAAACC[C/T]CATTTGGCTCCTGCT | 10213 |
rs148006236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310918 | ATTATAAATTCTCTC[A/G]GTGCATGCCACTAAA | 10213 |
rs148059839 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317393 | AAAAATATATGATTC[C/T]GTTTATGTAAAATTC | 10213 |
rs148127159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347507 | CTCTCTCTACTCAGA[C/T]GTTAGATCATATTAA | 10213 |
rs148217635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360171 | CTTTTTTCCACCCCG[A/T]AACATATATATATGC | 10213 |
rs148308079 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374613 | AAGGTCCGCTTGCAG[C/G]ATTTAGTTCATTTGT | 10213 |
rs148410300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338908 | GGATCATATAATAGG[A/G]ACTCTTCTTTTTGTC | 10213 |
rs148414767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378761 | TGTGTCATTTCATTT[A/G]ATTGATTTAAATTCT | 10213 |
rs148467905 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388807 | ATATAATCCGTAAGC[C/T]GTGTGTTTTATAATG | 10213 |
rs148531836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313941 | TACAGTTTAGTGGCA[C/T]TAAGTATATTCACAG | 10213 |
rs148587539 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319765 | TACTATAAGAAGCAG[A/T]TTTTGTTTCAGACTT | 10213 |
rs148657360 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161350789 | GATTTTGGATATGGT[C/T]TGAAGGTATTCCATA | 10213 |
rs148676457 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335800 | AGAATACAGGATTTG[G/T]CTTTGAATTTAGGCT | 10213 |
rs148710450 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306293 | TGAATTCTTTAAAGT[C/T]TGCATTGTTTATTGT | 10213 |
rs148746700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364342 | GTGTCTTTGCCTGCT[A/G]GGGTCTGGGAGTTTT | 10213 |
rs148797709 | snp | G/T | 2.70289e-05 | 0.0036761 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371341 | GAGTAGATTCTATCT[G/T]TATTGCCATCTACTG | 10213 |
rs148856062 | snp | A/C | 0.00698713 | 0.0586919 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367778 | CACATCTCTTCCTTT[A/C]TACAGATGTTAAAAC | 10213 |
rs148909452 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374196 | GGTCATTGTGAGGCC[A/T]TTCCTTAAGTTACTG | 10213 |
rs148925624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406945 | CATCTTTCATTGTCT[A/T]TCTACCATCTTTGTT | 10213 |
rs148941703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341423 | AGTTCTTTATATGTT[C/T]TGAATAGAAGTTCTT | 10213 |
rs149112728 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323567 | ACTCAGGAGGCTGAA[A/G]CAGGAGAATCACTTG | 10213 |
rs149129408 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346908 | CACACACATGCATTG[A/G]TCATTATTAAGCTGA | 10213 |
rs149186658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352848 | AGGAAGGTTATTTGT[A/T]TTCTGTGTTAACACC | 10213 |
rs149296686 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355832 | ACAGTTGTTGGATCC[A/G]CAAACAGAAATGTAA | 10213 |
rs149298444 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394475 | ATAAATGGGGCATTT[-/A]ATCTCGTTATCTTGG | 10213 |
rs149345050 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313598 | CAAGTGATCTGCCTG[C/T]GTTGGCCTCCCAAAT | 10213 |
rs149365718 | snp | G/T | 0.0818113 | 0.184966 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394081 | GGTCCAAGTGATTCT[G/T]CTGCCTCAGCCTCCC | 10213 |
rs149381567 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369162 | AGATACCCATTATAA[G/T]ACATTGTTCTTAGGC | 10213 |
rs149382234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332631 | TCACTTTAATGATGA[C/G]GTTTCAAGTATTACA | 10213 |
rs149420189 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402291 | GAGAAAAGACAACCT[A/G]CAAAGTGGGAGAACG | 10213 |
rs149439414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376562 | GACTTCCCTTCTTAT[A/G]TTTTGTGCATGCTAA | 10213 |
rs149561199 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364042 | TGGGCTTGGAGATGA[C/G]TGCAAGGTTTTATTG | 10213 |
rs149597012 | in-del | -/A | 0.0240643 | 0.107019 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361231 | GCTTCCAGTACTAAG[-/A]AAAAAATGAAAAATT | 10213 |
rs149625677 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337430 | ATCTTTACATTAACC[A/G]GTACCACGTGGTATG | 10213 |
rs149629704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343335 | TTTGTCATTTTGTGA[C/T]TGGCCTAGCATAATG | 10213 |
rs149668734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367305 | TTTTACCTGTTTTCT[A/G]CAGGTTTGATATTTG | 10213 |
rs149823294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358953 | TTCTATAAGGAATTA[A/G]TGTCCTATTTTTGTT | 10213 |
rs149897200 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396777 | TTCTGAAGTCTAGTA[A/G]TAGCACTTGGGATGT | 10213 |
rs149913793 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334713 | CTTTTTCATGCTCTT[C/T]AAGTATTTTTCTTCT | 10213 |
rs150066548 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326603 | CAGATGTTTGTACAC[C/T]AATATTCTTAGCAGC | 10213 |
rs150105666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355071 | GGAAAGGGATATAGA[A/G]TATGGTATAGGAATA | 10213 |
rs150174088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330379 | AATCTCAATATTCCA[A/G]ATGTATGGGACGTTA | 10213 |
rs150261378 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348061 | AGAAGCAGAAATGTA[C/T]CATAAACATGTATAT | 10213 |
rs150294073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315496 | GAAAAAAAGACTACA[A/G]AGATGAAGTCTCTAG | 10213 |
rs150347830 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322306 | GAGACATGACCCCAC[C/T]TTGAGTCCCAGTGCC | 10213 |
rs150420588 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400621 | TACAATAGCATGATC[A/G]TGGTTCACTGTAGCT | 10213 |
rs150437455 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337356 | TTGTTAGGAGTAGTA[A/G]TAGCAGCAGCTGTGT | 10213 |
rs150478555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410129 | TTATTACCTCACTGG[C/T]TTGGCCTACTGCATG | 10213 |
rs150546451 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339613 | GTGCCTATAAGCCAG[A/G]GTCGGAAACTTTCCA | 10213 |
rs150600005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346466 | ATCTTTGTCAGTGCT[C/T]AGTTTCAGTTGACTG | 10213 |
rs150672124 | in-del | -/ATTTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390492 | TGCTATTAGCTTAAG[-/ATTTT]ATTATGATTGGCCTG | 10213 |
rs150705395 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333595 | AATGAGAATGCAGTG[A/T]AAATGTTCAAGAAAG | 10213 |
rs150756369 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396521 | TTTTAAGTGAAATAA[A/G]CCAGGCATTGAAAGC | 10213 |
rs150794172 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351637 | TGTGCTAGTCAGGAA[A/G]GGTTGATTATGTTTC | 10213 |
rs150827211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318018 | CTTAACTTCTTCTGT[A/G]AGGTTTTCAAGCTTG | 10213 |
rs150878109 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324710 | TTGATCTGTGTTTTT[C/G]AAAAGTAATTCTAGT | 10213 |
rs150915262 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386376 | ATTGCTGCTCCCTTC[C/T]GAAACCTTGCTCTGT | 10213 |
rs150937805 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320331 | AAAACCCCTGGACAT[A/G]AAATAATGGTTTTAC | 10213 |
rs150973581 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389194 | GTGAGTCCATTAACT[A/G]GCTTCTGTATGTATT | 10213 |
rs150987836 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329694 | CAGAATTACAAGATG[C/G]CTTTAACGTTTTTCT | 10213 |
rs151026070 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342332 | TCCTACTTTGTTGAG[A/G]CTTTTTTTTTTTATC | 10213 |
rs151056639 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358787 | GTCTCCACCAAAGAT[A/G]CCAAAAATACAGGTG | 10213 |
rs151147118 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372606 | TTCTGATTCTTGCTA[A/T]ATGCCTATATTTCAA | 10213 |
rs151200341 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380901 | TACTTCCCAGGTCAC[A/G]TGCACTCTTAATTTT | 10213 |
rs151270611 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306739 | CCCAGCTAAATACTT[C/T]AGTATGGCTGGAGCA | 10213 |
rs151320046 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315140 | CAAACATTTATCCCC[C/T]GGGGACGTTTGGTAA | 10213 |
rs151326001 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353403 | CTCAGAAAAACAACC[A/G]TTGAAATTTAAACAG | 10213 |
rs180805389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379740 | TCAGACAGCAGTGAA[A/G]GGTTGACCATGCAAA | 10213 |
rs180822753 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359650 | TGTTCTCTGTTCTCA[A/G]TGAGCATACTAACTA | 10213 |
rs180834025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338728 | TTGACTGTATTTACT[C/T]AGGAAACCATCACTG | 10213 |
rs180842967 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400964 | CTACTATAAAATAAA[A/C]ATTTGTCAAAATGTA | 10213 |
rs180862262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320541 | TGATAAACTCTAATT[A/T]GTGGAACTCTTATTT | 10213 |
rs181047468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356340 | GTTGTTTAATACAAA[A/G]TTAAAGTATTAAAAG | 10213 |
rs181059423 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406053 | TGGAGATCCTTAAGA[A/G]TGTTAGTGAAGTGCC | 10213 |
rs181074316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375956 | AGAAGGTCGTGTCTT[G/T]TCTTTCAGGGGTGGG | 10213 |
rs181077188 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346117 | TGAACTCCTGGGCTC[C/T]GGTGATCTGTCCACC | 10213 |
rs181077688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396609 | TAGAGAGTAGAATTG[C/T]GGTTACCAGGAATGT | 10213 |
rs181093052 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364134 | GGACGCTGTCCTCCA[A/G]CTGCCCTGGCCAGAC | 10213 |
rs181096245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386198 | CATGCCATGGTGTTT[C/T]TATACAAATCTTTAT | 10213 |
rs181111706 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307721 | CTGTACCTAGACCTA[C/G]AGTGTAATATCAACT | 10213 |
rs181125179 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325148 | GGACATATGCAGCAG[G/T]GTATATAATGCCTGT | 10213 |
rs181300702 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401677 | ATGATCTTTATTATT[A/C]ATCTCTATTTCATGT | 10213 |
rs181321473 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340003 | TTCCAAGAAACGCAT[A/T]TGAGACTGATCTGAT | 10213 |
rs181322730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390481 | TAATAAAGCCATGCT[A/G]TTAGCTTAAGATTTT | 10213 |
rs181324460 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360151 | GGTTAAACAAAGATA[A/G]ACAGCTTTTTTCCAC | 10213 |
rs181335029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380849 | GTCTGGCAGTGCATG[A/G]CAGCAGAAGTAACGA | 10213 |
rs181344992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330076 | AATGCTAAATTTCTA[C/T]TTTGATATGCAATTA | 10213 |
rs181348510 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320927 | GACTATGTTTCACCA[C/T]GTTGGCCATGCTGGT | 10213 |
rs181358523 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369140 | TATATGTTATGGGTA[A/C]TTATGTAGATACCCA | 10213 |
rs181475091 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349972 | AACATTGAGATGTAG[A/C]TTTAATTTGTATTCT | 10213 |
rs181506863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315382 | TCCCATTCATCTTTG[A/G]TTTTGTAGTAATGTG | 10213 |
rs181507060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333553 | CAGATCTAGACACTA[A/G]CTGAGATCCATGGAA | 10213 |
rs181510486 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311266 | GTGAGCTGAGATTGC[A/G]ACACTACACTCCAGC | 10213 |
rs181523051 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387186 | TTTAAGACAATTTCA[A/G]TACTAAAACACACAA | 10213 |
rs181528326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407682 | GAAGAAATTTGGCAG[C/T]TGTGAGATTATAAAG | 10213 |
rs181534894 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354959 | TAGGTGTGCTATATT[A/G]GAGGAACTCAGTAGG | 10213 |
rs181667786 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374346 | TTGTTCAATTAATTT[A/T]AAAAAACAATTTAGA | 10213 |
rs181675887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346270 | GGACAACTTATTGAC[A/G]GCCTAGAGATAAAGT | 10213 |
rs181702083 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161308058 | ACCAAGTTAAATCTA[C/G]CTCAAATGAACCTTT | 10213 |
rs181724357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359387 | GAACTGTGCTTGCCT[A/G]GTTTTTATTTTTCTA | 10213 |
rs181729249 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331166 | TTTGTACCTGGTTTC[A/G]CGGTTTCTGGTTATT | 10213 |
rs181729293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378507 | CTCTTTTTTTTTGAG[A/G]TTTTCATTTCAATAG | 10213 |
rs181735067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400738 | TTTTGTAGAGATGGG[A/G]TTTCACTCTGTTGCC | 10213 |
rs181754964 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338572 | TAAAAAAGGCATTCA[A/G]TAACTTTATAATACT | 10213 |
rs181757010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311994 | TAATGTTGACTCACT[C/T]ACGATCTTCCACTGG | 10213 |
rs181761854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325904 | AGTGGAGAAGGAGAG[C/G]CCTGTTCATTAGATG | 10213 |
rs181773066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395643 | ATTTAATAATTATTT[A/G]TTGAAAATCTAATGT | 10213 |
rs181776272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364650 | TAGGAAAACAACAGC[C/T]TTAGTCACTGCTGGC | 10213 |
rs181896743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390659 | TAATTATTTGAATCA[A/G]TCAAAACTGAATTAG | 10213 |
rs181916156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374786 | GACTATACTTCTTTC[C/T]TGAGGCAAAAAGAAT | 10213 |
rs181924605 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396059 | ACACTACCATAGAGA[A/C]GACCATGGGAAGCCC | 10213 |
rs181928345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350716 | CACATAAATACATTT[A/G]TAGTTAATCACTAGA | 10213 |
rs181937735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319901 | TGCATTCTTGGATGG[A/G]TTTCAGTTGTTTTTC | 10213 |
rs181952209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315675 | TGATGGACTACTAAT[A/G]CCTCCTAGTATGATA | 10213 |
rs181953540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334331 | ACAAGAGTGAAACTC[A/C]ATTTCAATTAAAATT | 10213 |
rs181956517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355264 | TGTTGGCAATTATTT[A/G]TTGATTTATTATGCA | 10213 |
rs182120180 | snp | A/G | 4.99888e-05 | 0.00499919 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371328 | AAAAGGAAAGGTAGA[A/G]TAGATTCTATCTTTA | 10213 |
rs182128554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391445 | TTATGATAAGTCATA[A/C]AAATATTTCTTTTAG | 10213 |
rs182144969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331317 | GCTCGGGCTAGAGTG[C/T]GGTGGTGCGATCTCG | 10213 |
rs182147628 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312369 | GGCTGGTCTTGAACC[C/G]CTGACCTCAAGTGAT | 10213 |
rs182158509 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351848 | GGCCACTCTGCTTAC[A/C]TTTTATTGGCTGAAG | 10213 |
rs182207234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363367 | CATTTTGGGACATCT[A/G]GAAATTTATATTGTA | 10213 |
rs182215685 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369912 | TGGGCTTAACTCGAT[C/T]GCCAACAGCAGTTTG | 10213 |
rs182231258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324154 | TTGTCTTCAGTTTTA[A/G]TTTGTTAAGTCAATA | 10213 |
rs182322380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365776 | ATATCCATCACCTCA[A/G]TATTTATCATTTCTT | 10213 |
rs182335908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388943 | ATTTGGGAGGAAGGC[A/G]CTGGGGGCACACAGC | 10213 |
rs182339747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409408 | TGGGGGAAGACACCA[A/G]CCAATTAAAGGAATC | 10213 |
rs182349756 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309052 | TTCTGTTAGTGTTAG[A/G]TTTTCAGCTCCCTCC | 10213 |
rs182351452 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326728 | CTCGGGGGATTGATT[A/C]TCGGACCTCTGATGA | 10213 |
rs182354737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346880 | TCTTTCCCCAGACCA[C/T]GCATTGATTCCTCAC | 10213 |
rs182449672 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382497 | AAGAGGTTTCCCTAA[A/G]CTAGCCAAACTGCTA | 10213 |
rs182480785 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342477 | TGAAATTGGTTGATA[A/T]AATATAGGCGTTCAG | 10213 |
rs182487889 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306512 | TGAAATGACAAAACC[A/G]CAATTTTTTGCACCA | 10213 |
rs182505452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345480 | ACTCCTGACCTCAAG[C/T]AATCTGCCGACCTCA | 10213 |
rs182539688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404076 | ATGCCTGGCTATTTT[G/T]TTTTTTCTTTTAAGA | 10213 |
rs182704477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403412 | AATGGGGAGGTAACA[A/G]CTTAATGTGTACTAG | 10213 |
rs182733756 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321655 | GTATAAATTTGGAGG[A/T]CCTCACAACCTCCTC | 10213 |
rs182756019 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361222 | AGTTTTAAATGCTTC[C/T]AGTACTAAGAAAAAA | 10213 |
rs182777537 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315897 | TGCCCAGGCTGGAGT[A/G]CAATGGCGCGTTCTC | 10213 |
rs182796930 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410997 | ATAAATGAAATTTTT[A/T]AAAAAATCAGATGAT | 10213 |
rs182956592 | snp | G/T | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356490 | GTGGTTTCATCAGAA[G/T]TTTTGATTTTATGAT | 10213 |
rs182962323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376670 | GCTGATGAAAAGGAA[A/G]TGAATATATTACTTT | 10213 |
rs182986143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335669 | TTTGATTTACAAACC[A/G]TGTTGTAGTAAATAT | 10213 |
rs182988120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316386 | TTGGTATAAAGTTTT[C/T]CTCCTTAAATTATCA | 10213 |
rs183043422 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371871 | ATAATTCTGAAAACA[C/G]ATTAACTTGCAAAGC | 10213 |
rs183069729 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331766 | TTTCCTCTGGAATTT[A/T]AAAAAAATGGGGTGG | 10213 |
rs183086739 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334601 | TTTTAAAGTGCTCCT[C/G]TGTAGAGCATTAAAG | 10213 |
rs183167317 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353185 | ATCTTGGGTCCTTAA[G/T]ACTTAATATTTTATG | 10213 |
rs183173811 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403027 | CCCATATGAGCCAGC[A/T]ATTCTGCTCATAAGT | 10213 |
rs183202139 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360779 | CTGACCTCATGATCC[G/T]CCTGCCTTGGCCTCC | 10213 |
rs183202282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313494 | AGCTGGGATTACAGG[C/T]GTATGCCACTATGTC | 10213 |
rs183204237 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332003 | ATCAACATTTCTTTA[C/G]GTAGATAAAATGAAT | 10213 |
rs183204637 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381349 | ATGAATGCATCATAA[A/T]TTCTTAAAACATTAC | 10213 |
rs183284646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326118 | TCTTGGCTCATTGCA[A/G]CCTCCACCTCCTGGA | 10213 |
rs183299199 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352031 | GTAAACCTCTGTATC[C/T]CACTAAATTGAAATT | 10213 |
rs183309340 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392013 | GATCCCATTTTATAC[C/G]AGTTTTCAAGTTTGA | 10213 |
rs183316743 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313061 | TTTTGTTAATCTAAA[C/T]GGCTCTGTGAGATAG | 10213 |
rs183322349 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389398 | ACCTCCTAATGTACA[C/T]GAATATGAGCACAGA | 10213 |
rs183344903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347473 | GAAAAATTTGTGTTG[A/G]AATATTCTAGATGGA | 10213 |
rs183359976 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161308592 | GCGGCATCCGGCTCC[C/T]GCCCGTCTTCAGGTA | 10213 |
rs183374402 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397900 | GAGAAATAAATCGCT[C/T]ACCGTATTTTAAATA | 10213 |
rs183406339 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357510 | AAGTGATTTCAAAGT[C/T]GCTTGTAGGAATTTA | 10213 |
rs183409319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376993 | ATAGAGTCGTTTATT[A/G]AATGACTGGAACGTG | 10213 |
rs183547434 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397016 | TATCTTTTAGTAGAG[A/G]CGGGGTTTCACCATG | 10213 |
rs183553191 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366767 | TGTGCAGGTGAATGT[C/T]ATAGTCAAGAGAAGT | 10213 |
rs183582320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327067 | CTGACATATGCTACA[A/G]CATGAGTGAACCTAA | 10213 |
rs183612300 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392504 | TAATCTAATCTATAT[C/G]CTGGGGGGGAGGATG | 10213 |
rs183653107 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393816 | ACTTTAAGAAAAACC[A/G]TCTTAAAATATAAAC | 10213 |
rs183657423 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321440 | AGACATATTTTTTTT[A/T]ATATCAGTGTCCAAA | 10213 |
rs183676894 | snp | A/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306887 | AAAATTTTTACCAGT[A/G]AGGTGGAGAATGGAT | 10213 |
rs183677116 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332389 | TATGTTGTTTTATTT[A/T]AAAAAATTATTTTGG | 10213 |
rs183680584 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354195 | TGTTTATATTTTCTG[A/G]TTTCTGAAGTTTGAA | 10213 |
rs183684830 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324233 | ACGAACAAGAATATC[A/C]ATGCCTAATCCAGAG | 10213 |
rs183690714 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373021 | TAGAGTAAATAAATG[C/T]AAATGTAAATAAATG | 10213 |
rs183822621 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372472 | CATTATCATGTATAA[A/T]AATTGAGGTCTTCTC | 10213 |
rs183846639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340954 | CTTCCGATGATGGCC[A/C]CTTCTCACCATCCAA | 10213 |
rs183884105 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390408 | CACTTGATGTTGTCA[C/G]AGTTAGATATGGGGG | 10213 |
rs183914363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336765 | ATTTTTAATAGAGAT[C/G]GAGTTTCACCATGTT | 10213 |
rs183919464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349199 | TCTACAGTCTGTTGT[C/T]TTATAAGTATGCGTC | 10213 |
rs183923869 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368710 | AATATTTCTCTTACT[C/G]AGCCTTGTAAAAGAA | 10213 |
rs183925105 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408342 | TAGTGGATCAAAAGT[C/T]GGTAGCTCCTTTGAT | 10213 |
rs183947758 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161328314 | AGCTAAAATGAATGA[A/G]CTAGGTTCTATATAC | 10213 |
rs183958129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365259 | GGCCACTGACATGTG[A/G]CTTGCTTCCTCTCTC | 10213 |
rs183991549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382977 | GTCATTCTATTGCAT[C/T]ATGCTGTAAATACAC | 10213 |
rs184020633 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323239 | TTTAACTAAACTTCA[A/G]TATTCCACACTTACT | 10213 |
rs184021724 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343286 | TACGAATCTCACTAT[G/T]CAAAGGACCTCACAT | 10213 |
rs184028917 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361831 | TGTTTTAATTGTTAC[C/T]CGTAAGCAGCATACA | 10213 |
rs184077905 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388109 | TGACATTTTGGATTC[G/T]TAAGTGTCACAGTAA | 10213 |
rs184111460 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317227 | ATGGAGATTTTATTT[A/G]TAAATGTTGCTATTA | 10213 |
rs184112844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346650 | TACTTGGAAACTGTT[C/T]GATTCTTTCTAGTTT | 10213 |
rs184160674 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345648 | GATGTAGTTTTCTTC[A/G]TGTTTCTTGTGCTTT | 10213 |
rs184171215 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385389 | AGATGCACGTCGATC[A/G]TGCCTTGTCCACTGT | 10213 |
rs184216012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378061 | TAGCCATTGTTATTT[A/G]TGAGGATATTTCTGG | 10213 |
rs184221922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400477 | TACATGGATTTTTCT[C/T]ATAAATATATTAGAA | 10213 |
rs184238749 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319158 | TTTTAGGAAAAAAAA[A/C]CCCTCAAAATAGCTT | 10213 |
rs184244165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338145 | TTGTGGTGAGTTGTA[A/G]AGCCCTTGATGAAGC | 10213 |
rs184244309 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358905 | TCTAGCACATGAAGT[A/T]TCTTGAAAACCCTTC | 10213 |
rs184244763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313987 | ACCACCATCCATATC[C/T]AGAATTTTTTCATCC | 10213 |
rs184275266 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405570 | ATCATGCCTATATTG[A/G]TGTTTAATTAGTGAT | 10213 |
rs184307480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363875 | GCTGAGGCCCCAGTG[G/T]GTGTGTGTTATAGGG | 10213 |
rs184427453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374432 | CATAAATAATGAAAT[A/G]CACTATATGATAAAG | 10213 |
rs184460823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383479 | ACAGATCATGATATC[C/T]ACTGAACTAGTATTT | 10213 |
rs184464505 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405110 | CCCTCTACCAATTTG[G/T]TTATAACTGACACTC | 10213 |
rs184486940 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400066 | CCTATACTTTATGTA[A/G]CGCCTGAATTATTTT | 10213 |
rs184506855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318722 | GTAATTACCACCAAT[A/G]TTTTTGACATACTGA | 10213 |
rs184515451 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358631 | TGACTCATACGTTTT[C/T]CTCCTTAAGTTTTTT | 10213 |
rs184608988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161377213 | CTGGGTAGTCCTAAT[C/T]ATAAATTATACACAC | 10213 |
rs184642641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337717 | GTAAGTAGTATATTT[C/T]TCAAAGTGTATAAAC | 10213 |
rs184653502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311168 | ACAAAAATTAGCCGG[A/G]CATGGGGGCGTGTGC | 10213 |
rs184693877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378585 | ATGGATATTCAGTGA[C/T]GAATGAGACACAAAC | 10213 |
rs184704089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400877 | AAAAAAAAACAAGGT[A/G]TGTCACAAACGCATA | 10213 |
rs184781910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333234 | TTTTATAGGAAGTTT[A/C]CTTTTTTAGTAAGTT | 10213 |
rs184792936 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373351 | TTGTATCACTTGTTG[A/G]ACCTAATGTCTAGAT | 10213 |
rs184867522 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395046 | GGTATCCTCAAGGCA[A/G]AAAAAGAATTACTTT | 10213 |
rs184902582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354372 | CACCTGAGCCCTCCA[A/G]GTGGCTGAGACTACA | 10213 |
rs184914719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375233 | AAGATAAATTATATA[C/T]ATTTAGTGTTAGTAG | 10213 |
rs184915187 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348620 | CTATACGATTGTTTT[C/T]ATGTACAATTTTAAG | 10213 |
rs184924296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346807 | GGTGGGAACAGGAAC[G/T]CTTTCCAGTGCTGTG | 10213 |
rs184924524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396189 | ACTTGAACATACAAA[G/T]AAATGTTACCCTAGG | 10213 |
rs184926804 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315174 | TTGGAGACATTTTTG[A/C]TTGTCACAGCTGGAT | 10213 |
rs184941968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310239 | CCATGTGCTTGTTAA[G/T]ATATAGTTTGTGAAC | 10213 |
rs184952591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355931 | GTGTTAAAATAGGCA[A/T]ATACAAATTAGTTTA | 10213 |
rs184963012 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327948 | ATTCTCATGTAAGCT[C/G]TGTGTGTGTGTGTGT | 10213 |
rs185082764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309395 | TATTATGGAAAGGCA[A/G]GGGAAAGGGTTTAAA | 10213 |
rs185160994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371393 | ATTAAATAAAAATCA[A/G]TTTTGTTCAAAGCAG | 10213 |
rs185165495 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391504 | TCTTCAATAAAAAGG[C/T]CTTTTGTAATTAAAT | 10213 |
rs185190886 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351849 | GCCACTCTGCTTACA[C/T]TTTATTGGCTGAAGA | 10213 |
rs185281735 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395739 | TTAAAATACACATTT[A/G]TACATTATGCAGTGT | 10213 |
rs185324023 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323712 | GGCTACAATAATTAA[A/G]TTTGTCCTCAGTCCT | 10213 |
rs185452321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320681 | AACATGAAACGTTAA[G/T]TGTATTTTTTTGCCT | 10213 |
rs185461887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343738 | GAGCCTAAGGCTGGA[A/G]AATCGCTTGAGCCTG | 10213 |
rs185564818 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367404 | AAATATCAAGTTTAT[A/T]CCACATGTAACTTGA | 10213 |
rs185568360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338590 | ACTTTATAATACTTT[C/T]TGAATTTTGAGAATT | 10213 |
rs185662196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407224 | TTAATATGTTTTGTC[A/G]ATGTTTCCATTTATG | 10213 |
rs185667538 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359388 | AACTGTGCTTGCCTG[G/T]TTTTTATTTTTCTAT | 10213 |
rs185681061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346181 | AGCCACCGTGCTCGG[A/C]CATTTAATTTTTTTG | 10213 |
rs185690037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319948 | TTTGATGATTTCTCA[C/T]GTTTCTTTGTTGTCA | 10213 |
rs185691572 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364476 | TGGTGGTGGTGCCTT[A/T]GCCAGGGGCCACACC | 10213 |
rs185708179 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389998 | GCCTCCCAGAGTGCT[A/G]GGATTACAGGCTTGA | 10213 |
rs185721790 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307805 | TCATGAGTAAAATGT[C/G]ATTGCCGATAATTAC | 10213 |
rs185723683 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325389 | GTATGGATTTTTTGT[A/G]TATTCACTAATAACT | 10213 |
rs185764784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388253 | TAGAGTTAAGCTATT[C/T]GGAAAACATTGTTTC | 10213 |
rs185805851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315787 | ACCTACACAGTAATG[A/G]CATGATAGAATGAAT | 10213 |
rs185900544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402397 | AAGCCCAGCACTTTG[C/G]GAGGCCACAGCAGGA | 10213 |
rs185901555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408610 | CCTGTTTGATATTTT[A/C]AATACTTTCTGTGTA | 10213 |
rs185923724 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340545 | CAGTCCAGGGTCTGA[A/G]CTCTAACTCTTAAAA | 10213 |
rs185930576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360753 | GTGTTAGCCAGGATG[G/T]TCTCCATCTCCTGAC | 10213 |
rs185941920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381026 | CACCTTTCATTTTTA[C/T]AATCATTTAGAGATT | 10213 |
rs185948599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334389 | GCCTGGCCACAGTGT[A/C]TTTTTTGTTCGCTAA | 10213 |
rs185970058 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320973 | TCAAGTGATCCACCT[A/G]CCTCGGCCTCCCAAA | 10213 |
rs185995102 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334226 | CTGTAATCCCAACTA[C/T]TCAGGAGGCTGAGGC | 10213 |
rs185997176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315587 | ATGATGTAATAACTA[C/T]AATTTTTTTCACTAT | 10213 |
rs186009851 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354981 | CTCAGTAGGCCTAGG[A/G]AAAGAAACTTTTCAG | 10213 |
rs186064550 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359757 | CTAAAATTATAAACA[A/G]TGGAAGTGAACTAAG | 10213 |
rs186072060 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331480 | GACCAGGCTGGTCTC[A/G]AACTCCTGACCTGGT | 10213 |
rs186077653 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401436 | ACGTAGTTAAATGGA[C/T]GCAACTAGCTGCAAG | 10213 |
rs186177953 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407949 | GTTAAGATTTCTTAC[A/G]TGTGAAATTCTCAAT | 10213 |
rs186195916 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312393 | AAGTGATCTGCCCCC[C/T]TCGGCCTCCCAGAGT | 10213 |
rs186203233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380009 | GTTGTGAGTCAGTCA[G/T]GCGCTCCACAGCAGG | 10213 |
rs186211002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369949 | GGCAATTTTAGAAGC[G/T]TGATTGGTATGAGGT | 10213 |
rs186228040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339277 | TGTGTGAGAGTTCCC[A/G]TTCTTCCACATCCTT | 10213 |
rs186238690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311996 | ATGTTGACTCACTCA[C/T]GATCTTCCACTGGAA | 10213 |
rs186242556 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331266 | CTTTGGAATTTTTTT[A/T]TTTTTTTTATTTTTA | 10213 |
rs186246973 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350735 | TTAATCACTAGATTG[C/G]TGTAATGCAGGTATA | 10213 |
rs186318963 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376061 | TTTACTCAAATAGTA[A/G]TCTTCTTTTGAGCTT | 10213 |
rs186344704 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334774 | AGGGTCTCACTATAT[C/T]GCCCAGGCGAACTCC | 10213 |
rs186387485 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403101 | TGTATATGAATGTTC[A/G]TAGTAGCACTGTTCA | 10213 |
rs186464784 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356396 | AGATAAACAGTACAA[G/T]GGTAGTTAGTTGTAT | 10213 |
rs186493789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326301 | CTCCGAAAGTGCTGG[A/G]ATTATAGGCAAGAGC | 10213 |
rs186511395 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396712 | CAATATGCTTGGCTA[A/G]CATGCATAGAACGTG | 10213 |
rs186522516 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316002 | GCCTGCCACCACGCC[C/T]GGCTAATTTTTTTGT | 10213 |
rs186544992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161308749 | CCCGGCCTCCTTCAT[G/T]CTCTTCGCCTGCTCT | 10213 |
rs186573005 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390491 | ATGCTATTAGCTTAA[G/T]ATTTTATTATGATTG | 10213 |