SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs186604407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350089 | CATTTTTAAAGAAAT[A/G]TTGGTATGTTTAGTA | 10213 |
rs186625401 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161377142 | AAGATATTTAGCATA[C/G]CTGCTATATTTATAA | 10213 |
rs186639113 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311329 | AGGAAAAAAAAAATT[G/T]CATCTATATTGAACA | 10213 |
rs186720593 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321780 | CCAGTGAAATGAAGA[C/G]ACACAGGATGGGGTC | 10213 |
rs186733913 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342747 | TTTGCTTAATAATTT[C/T]CTCATTTGTTCTTTT | 10213 |
rs186819770 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394686 | GCAGTAAACAAGTAA[A/G]CAAAAATTTCAGGTC | 10213 |
rs186842057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369377 | TAAGACAGTCCTTTT[A/G]AAGTATATATATGAA | 10213 |
rs186873454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326088 | TGTCACCCAGGCTAG[A/G]GTGCAGTGGCATGAT | 10213 |
rs186899255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364864 | ATGCTAGCACTTTGG[A/G]AGACTAAGGCGGGTG | 10213 |
rs186942718 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366159 | AAAAATAAGCAATAA[A/G]ACTGCATTAGGTGAT | 10213 |
rs186944973 | snp | A/G | 1.76802e-05 | 0.00297318 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318882 | GGGCCAGGTTAGTAT[A/G]TAGTCTCTTGAGCAT | 10213 |
rs186951449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388950 | AGGAAGGCACTGGGG[A/G]CACACAGCAGGTGAG | 10213 |
rs186958431 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410208 | TCCTGCCAGTGTTTC[C/T]CAGTGTTTTTCACCT | 10213 |
rs186969414 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326941 | TTATTGTTTTTTCCC[C/T]CCGATATTTTCTATC | 10213 |
rs186982692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347087 | TGGGTTTCTTCCCCT[C/T]TGCACTGCAGTCCAA | 10213 |
rs187042848 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387358 | GATCTTTAACTCTGG[C/G]ATCAGAAACCTTTCA | 10213 |
rs187076450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346350 | GTACATTGTCATTTT[C/T]ATCCCAAGAAGTTTT | 10213 |
rs187123581 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161308372 | CGCTTGACTCTCCGT[C/G]GTCTCCAATTGGCCG | 10213 |
rs187177510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361914 | GACTTTAATCCATTT[A/G]TATGTTTTCATAACT | 10213 |
rs187183940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383131 | ATTAATGAGTCTATT[C/T]TGATAGGTTGCTCTA | 10213 |
rs187188694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404324 | GTAGATGCTCAATAA[A/G]TATTTATTAAATGAA | 10213 |
rs187212443 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323334 | TCCATTCCTACAAAA[C/G]AACTAAGTTTTATTT | 10213 |
rs187215857 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343340 | CATTTTGTGACTGGC[C/G]TAGCATAATGTCATT | 10213 |
rs187345926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391256 | CCTGGTATGTGATTT[A/T]AATTCGAATTTTTGA | 10213 |
rs187445212 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357803 | AGCTTAAGTACCTCT[G/T]TAGTTATACTGGTGC | 10213 |
rs187464274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318213 | TATCTGTGTAGGTTC[C/T]AGAACACTATCTTAA | 10213 |
rs187554630 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397577 | GGATCATAGTTAAGA[C/T]TGTTGTTGGTTATTA | 10213 |
rs187587550 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336484 | TAGTATTTTCAGTGA[C/T]GTTACTTATTTGAAA | 10213 |
rs187587863 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357205 | TCAGTTAATTTAACC[A/G]CATTTAAAATTTGTA | 10213 |
rs187595352 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376822 | CTTGGAATTCAGTGC[A/G]TTGCAATAGTTTTTT | 10213 |
rs187618431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316717 | TGATTTAGAATATGT[A/G]TCAATATACTTCATT | 10213 |
rs187650804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403523 | GGTTAATTTTATGTT[A/G]TGTGAAATGTACCTC | 10213 |
rs187676829 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336805 | GGTCTCAAACTCCTG[G/T]CCTCAGGTGATCCAC | 10213 |
rs187830016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353468 | CTTTAGTTAGCTCAT[C/T]TTATTGTTTAAAAAG | 10213 |
rs187838229 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372535 | TTTCAGAGGCAAAAA[C/T]TATCCACAAAAACAG | 10213 |
rs187844288 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393160 | CAAGGGAATCCTTGT[C/G/T]CAGGTATGATAGGAA | 10213 |
rs187864926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313495 | GCTGGGATTACAGGC[A/G]TATGCCACTATGTCT | 10213 |
rs187884460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161377417 | TATCAGTTTGAAGTT[C/T]TATAACACTCTCAGA | 10213 |
rs187915155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337929 | ACTACTTAATTGTTA[C/G]AAGAATTATACTCTC | 10213 |
rs187918956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382539 | ATAAGCTGTCTACTG[C/T]TGCAGTGACCTCTGA | 10213 |
rs187938934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309298 | CTGTCAAAAGAAAAA[G/T]AATGTAAACTTTTGA | 10213 |
rs188071230 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161398663 | CTTTTTTTTCCCAAG[A/C]ATGTAGTGCTATAAA | 10213 |
rs188095062 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310967 | CATATCTTTGGGTTC[C/T]GCATCTGTAGATTCA | 10213 |
rs188111576 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161327981 | GTGTGTGTGTGTGTG[A/T]GTGAGATGTTGGTTA | 10213 |
rs188176118 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400171 | TAGAAAGGTATGTCT[C/G]ATATTTCAAGTCCAA | 10213 |
rs188179708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352700 | TGGATTCCCTCTCCT[C/T]TGTGTGGTGCTTTCT | 10213 |
rs188193772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392161 | TTGTTTTTTGATATT[A/G]CAATCTGAACCAGTT | 10213 |
rs188204300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313296 | AAACAACTGTATTAG[A/G]AATGTTAGTAAAGCT | 10213 |
rs188210214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358637 | ATACGTTTTTCTCCT[C/T]AAGTTTTTTCATGTT | 10213 |
rs188314993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346088 | GGGTTTTGCCATGTT[G/T]CCCAGGCAGTTCTTG | 10213 |
rs188320879 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364051 | AGATGAGTGCAAGGT[G/T]TTATTGAGTGAAAGT | 10213 |
rs188339350 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307152 | CTCCAGCCTGCGTGA[C/T]AAAGCAAGACCCTAA | 10213 |
rs188347524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324301 | AAGTGCCTAGTACAC[A/T]TTAACTACTTTGAAT | 10213 |
rs188353939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373038 | AATGTAAATAAATGA[A/G]TATGTATTTTATTTT | 10213 |
rs188402364 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161411202 | TTTAAGTAAGGTCTG[C/G]CTTTCTTTACTAGTT | 10213 |
rs188431811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366934 | TCACACCTGGGGCAA[C/T]TGTGTTAAATTTGTT | 10213 |
rs188466169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327157 | TTACATGAGGTACCT[A/G]GAGTATCAGATTCAT | 10213 |
rs188473278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372103 | ATTCGATTTTGCTCA[A/G]CCACAGGGAGAGTGG | 10213 |
rs188501279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331772 | CTGGAATTTAAAAAA[A/T]ATGGGGTGGGGGAGC | 10213 |
rs188557904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390410 | CTTGATGTTGTCAGA[A/G]TTAGATATGGGGGCA | 10213 |
rs188586078 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349624 | TAGATCCTATGTGAA[A/G]TTACAAACAAGTGAA | 10213 |
rs188594758 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368964 | CTAATTTGGATCTAC[A/T]GATTTTATCCATCTT | 10213 |
rs188703559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381646 | CAAATTTTAAAATAA[A/G]TAGCATATTGGATGA | 10213 |
rs188712587 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348369 | ATTACAAAAATGAAT[A/G]GGCCTGGCCATGTTC | 10213 |
rs188727803 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389517 | TATTGAAATGAGTAA[G/T]GATTTAATATACACT | 10213 |
rs188734142 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309739 | GAATTTGTCCCTAAA[C/T]CTTGCCAAGGGAAGA | 10213 |
rs188734555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341384 | GATCCCGCCGCGCCC[C/T]GTCCTTTGTTAATGA | 10213 |
rs188761391 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315330 | TGGCTAATTTTATTG[C/T]CATCATTAGAGACTA | 10213 |
rs188807787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407250 | TTATGTAAAACATTG[A/G]ATAGTGGGAGAAGCA | 10213 |
rs188842561 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364618 | CTGGTTTTTGCTATT[C/T]TGAACAGGTGAGCAT | 10213 |
rs188846837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386305 | GATTAATTAAAAGGA[C/T]AGAAATACCATGTTT | 10213 |
rs188969177 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378423 | TATAGATAATGGATA[C/T]TTTTCTTTTCCTTTA | 10213 |
rs188978865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400499 | ATATTAGAATCTTTT[C/T]TGAGATGTACAACAA | 10213 |
rs188988168 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319860 | TATGACTTTTATAAA[G/T]TTGAAATCTTTTTGT | 10213 |
rs189003510 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338249 | AAATTACGAGAAATG[A/G]AGTTCTGAAACTGCG | 10213 |
rs189006000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359246 | CAAAGTGCTGGGATT[A/G]TAGGTGTGAGCCACT | 10213 |
rs189019316 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360930 | ATTTTTAATTTGCTT[A/G]TGTACTGACTTCTTG | 10213 |
rs189049888 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321442 | ACATATTTTTTTTTA[A/T]ATCAGTGTCCAAACA | 10213 |
rs189175671 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405698 | TTTGAAATCCACTAG[C/T]AGTTATGCATTGATT | 10213 |
rs189220291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395971 | AGAAATGCAGACTTT[C/T]AGACCTAATGGCTCA | 10213 |
rs189223519 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332809 | TGTGCTGGGATTACA[A/C]CAGAGTGCTAACAGC | 10213 |
rs189238540 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315621 | ATTATTTTCCATATT[A/C]TTGTCATTTTAGTGT | 10213 |
rs189244836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334312 | TTGCACTCCAGCCTA[A/T]GCAACAAGAGTGAAA | 10213 |
rs189251216 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355216 | GAACCTAGGTATATT[C/T]CAGCAGTGGGTGAAA | 10213 |
rs189503373 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386153 | GACACTTAATATCCT[C/G]TTGAGTGATTGTTTT | 10213 |
rs189515553 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354280 | GGAGACAGAGTCTCA[A/C]TCTTGCCCAGGCTAG | 10213 |
rs189519061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311172 | AAATTAGCCGGGCAT[A/G]GGGGCGTGTGCCTGT | 10213 |
rs189544818 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314600 | ATTCTGTCTCTATGG[A/G]TTTATTGGATATTTC | 10213 |
rs189628122 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348722 | TAAGATGAGAATAGC[A/G]GTGACATCTGAGGAT | 10213 |
rs189640348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368396 | TTAAAGCAAAACAAA[A/G]CAATAGCAAACCTGA | 10213 |
rs189692185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365772 | TAACATATCCATCAC[C/T]TCAATATTTATCATT | 10213 |
rs189698838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388361 | CCTGAGGCCCATAAA[A/G]TTGAGTTGCCCAGGT | 10213 |
rs189722883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326442 | AGAAATTAGAACTCT[C/T]GTACATTGATGGTAG | 10213 |
rs189724869 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346812 | GAACAGGAACTCTTT[A/C]CAGTGCTGTGTGGGA | 10213 |
rs189733750 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396429 | GTATAGATATACATA[C/T]AATGGAATACTATTC | 10213 |
rs189750955 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329484 | CAGTATTTATATGCT[C/T]ATGAATATTCTGGTT | 10213 |
rs189753169 | snp | A/G | 2.64967e-05 | 0.00363973 | missense | PSMD14 | GRCh38.p7 | 2:161395135 | ACACTTCAGGACTAC[A/G]GTGAACATTGTAAAC | 10213 |
rs189756209 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161308796 | GGTCAGGTCTGGATG[A/T]CGCCTCCTTTCTCCA | 10213 |
rs189781043 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354457 | GTCATGTTGCCCAGG[C/T]TGCTGAATGATGTTT | 10213 |
rs189966519 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371549 | TGTAATTTTCCTGAA[C/T]ATTTATCTTTAAATT | 10213 |
rs189976930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391976 | CAGTTTTAGGGTTTT[C/T]AGATAATTTGTACTA | 10213 |
rs189996268 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373710 | AGTTGGGTCTCTGTT[A/C/T]GCTTTTTATAAAACC | 10213 |
rs190013226 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330680 | TGAAAGTATGCCACC[A/G]GAGCAGGGCAGTGGT | 10213 |
rs190029187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333272 | TCAAATGCCTGTGCA[C/T]GTGATTAGATGTTAG | 10213 |
rs190036511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369839 | TGGTTCAATTATTTC[A/G]TATTTCTGGTAAACA | 10213 |
rs190126206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339399 | GACTGATGATGGTGA[A/G]CATCTTTTTATGTGC | 10213 |
rs190162027 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320882 | AGGCGTTCACCACCA[C/T]GCCCAGCCGATTTTT | 10213 |
rs190247091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390526 | GTTCACCTTGGAGAC[A/G]GAGTGAGGTGAAAAA | 10213 |
rs190282690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350437 | GTCCTAAAACTAGAT[A/G]TGATAATGTTTAATT | 10213 |
rs190299655 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383694 | TCACAAATGAATTTA[C/T]TGAAATCTTGAAATG | 10213 |
rs190305102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311492 | TGCAAATAGGGTACT[A/G]TGCCATTTTATATGA | 10213 |
rs190322846 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306328 | GACCACTCAGGTTTC[C/T]GCTCAGTTAGCTTAG | 10213 |
rs190330754 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345303 | GCTGGAGTGCAGTGC[C/T]GTGATCTCAGCTCAC | 10213 |
rs190404276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346217 | TCTTCTATTAACCCC[A/G]TCTAGTGTATTTTTT | 10213 |
rs190414888 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316311 | CTCTCAGAAAAAGAT[C/T]ATTAAAAAACAGTTT | 10213 |
rs190415296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335098 | AATTCAGGGAGTTTT[C/T]ATGAGAAACAAGGTA | 10213 |
rs190537529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359570 | TATACAGTGTATAGT[A/G]CATTTTGCTCTCTAT | 10213 |
rs190545092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362828 | TCTCAAGATACAGTT[C/T]TTTATTCATTGATTA | 10213 |
rs190556394 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400887 | AAGGTATGTCACAAA[C/T]GCATAAAATATAGGA | 10213 |
rs190559957 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405356 | CCCTATGTCCCCATC[A/G]TGCTTTGTGCACACT | 10213 |
rs190566671 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320339 | TGGACATGAAATAAT[A/G]GTTTTACTGACCACA | 10213 |
rs190583813 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390215 | GTCTATTAGTTAGAG[A/C]AGTGGTGGTTATTTT | 10213 |
rs190616630 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402575 | AGGCCCAGGAGGTCA[A/G]GGCTGCAATGAACCG | 10213 |
rs190637750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340554 | GTCTGAGCTCTAACT[C/T]TTAAAACTCTTCAGC | 10213 |
rs190654032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360778 | CCTGACCTCATGATC[C/T]GCCTGCCTTGGCCTC | 10213 |
rs190660528 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381064 | TATAGTGATGGTTTT[A/G]TGTTTTAAAATATGT | 10213 |
rs190685211 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321121 | ATAGTAGTAAAAAAG[G/T]AGACACAAATTGGCC | 10213 |
rs190774590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409303 | TTAGAGCCTTATTGG[A/G]TTATACTGAGTGAAG | 10213 |
rs190794543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375249 | ATTTAGTGTTAGTAG[C/T]GAGCAAGATCTTATT | 10213 |
rs190800720 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379479 | TTCCCTAAGGAAATA[C/T]ATCTTAAAGCGTCAC | 10213 |
rs190818186 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334399 | AGTGTCTTTTTTGTT[C/T]GCTAAGGTTTGTGTG | 10213 |
rs190836457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338680 | TTGACATACAGTAAA[C/T]GATAATATTTAAAGT | 10213 |
rs190863874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397602 | TTATTACACCAAAAC[A/G]TAGTATTTCCCTTTT | 10213 |
rs190887845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336521 | GAATTACATTGAAGA[A/G]GTAAACTTTGCAACT | 10213 |
rs190891970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357321 | ACAGGTTTTATATCA[C/T]TGGTTGCTTAGATTT | 10213 |
rs190904348 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376981 | TTATATGTCAGCATA[C/G]AGTCGTTTATTAAAT | 10213 |
rs191011970 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370449 | CCTCTGTTTAGCATA[C/T]GGAGTTACTGTCTAG | 10213 |
rs191022356 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391329 | TGCAGCACAAAATAA[A/G]GGAATATTTTATTGG | 10213 |
rs191035316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356301 | CAGTAGAAATAGTTT[A/G]CATGCAGCTTGTTTT | 10213 |
rs191044083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331293 | TTTAAGACGGAGTCT[C/T]ACTCTGTTGCTCGGG | 10213 |
rs191055625 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315865 | TTTTTTTTTTTGAGA[C/T]CGAGTTTCACTCTTG | 10213 |
rs191057693 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312886 | AATGTGAAATATGCC[C/T]AGCATTTTGAAACCC | 10213 |
rs191059030 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351730 | ATGTCTACATGGGTC[A/G]TCTGGGTGCTCTGTT | 10213 |
rs191071355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380021 | TCATGCGCTCCACAG[C/T]AGGTTCTGTTGAAAG | 10213 |
rs191076783 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351850 | CCACTCTGCTTACAT[C/T]TTATTGGCTGAAGAG | 10213 |
rs191275722 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401588 | TTCTGCCATAGAAAT[G/T]TTTTCCAACAACCTT | 10213 |
rs191311677 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359822 | ATGGGATGGCGTACT[A/G]TACTGGAAAGTATAT | 10213 |
rs191315938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331667 | ACAGTCAGATACTGT[C/G]AATAGGGAATGTCAT | 10213 |
rs191319369 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356470 | AATTGAGGAAACTGA[A/G]TGTAGTGGTTTCATC | 10213 |
rs191333756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396799 | TTGGGATGTCAGGAT[A/G]AGAGGTTTTTTTGAG | 10213 |
rs191377677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325397 | TTTTTGTATATTCAC[G/T]AATAACTTTTTCTGG | 10213 |
rs191388175 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348902 | TTTAAAAGAAATAAA[C/G]TAAATAACAGTGGTT | 10213 |
rs191392487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368672 | CATGTATTTTTCCAA[A/G]CGATATTTCTTCTTT | 10213 |
rs191402511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390401 | ATTTGAACACTTGAT[A/G]TTGTCAGAGTTAGAT | 10213 |
rs191422486 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161328241 | AAAGCATTGTTTGTA[C/T]ATTAAAAATTGCAAA | 10213 |
rs191513013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382753 | TGTGTAAAGTTTTTT[G/T]GTTAAGTTACTGTTT | 10213 |
rs191528352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322820 | TATTTGGGAGTTGTA[A/G]TAGGGCTAGTAGGTA | 10213 |
rs191545126 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342750 | GCTTAATAATTTTCT[C/T]ATTTGTTCTTTTGTC | 10213 |
rs191547172 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361806 | ATTGACAAATTTTGC[C/T]CAGTCTTTTTGTTTT | 10213 |
rs191560789 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376184 | ACTTAGGGGTCAGGC[C/T]TGCATTAAAATCCCA | 10213 |
rs191623155 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161308024 | CCCCCCTCTTTTAAA[A/C]AAATTTTCTTCTCAG | 10213 |
rs191789616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366350 | ATGCTTCCAGTAAAT[A/T]TATGAACTTTTAAAA | 10213 |
rs191794193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338132 | CAAGCACATAGCCTT[A/G]TGGTGAGTTGTAGAG | 10213 |
rs191795690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319050 | CATGTGGAAAACATT[C/T]ATTGTCTTAGTTTAC | 10213 |
rs191800678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389112 | AAAATCAAGTAGATT[A/G]TGCCTTCAGACACCA | 10213 |
rs191810211 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410438 | GTAAGAATATAATCA[G/T]TTAAATTATAATTTT | 10213 |
rs191810376 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358654 | AGTTTTTTCATGTTT[A/C]AAGAGCCTGGCCGGG | 10213 |
rs191838417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387696 | CCTATATATTTATAC[C/T]AGGATATTAGCATTG | 10213 |
rs191865487 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346603 | TTATTCTTAGAAATA[G/T]TCTTGATATTTGTTA | 10213 |
rs191894240 | snp | A/T | 0.00318978 | 0.0398085 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161308416 | GCCGAAGCAAACTAG[A/T]GAACCCGGAAGTGCT | 10213 |
rs192042443 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161362160 | AGCCTCAGCCTTTCG[A/G]GTTCAAGCCATCTTC | 10213 |
rs192052605 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403219 | CTCAGTCATAAAAAG[G/T]AATGGAGTGCTGATA | 10213 |
rs192055289 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383338 | TTCCTTTAATCTTAG[C/T]GTAAAGTAGTCATTT | 10213 |
rs192066485 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404825 | CCCCTGACTTTTTGG[C/T]AACTACACACTCTGC | 10213 |
rs192067471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321580 | ACCCTTACTTCAGAT[A/G]CCAGCTATACTTCAT | 10213 |
rs192075631 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161361216 | AAATTTAGTTTTAAA[G/T]GCTTCCAGTACTAAG | 10213 |
rs192091616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343464 | GTCCATTCATCTATT[A/G]ATGAGCAGTTGGGTT | 10213 |
rs192150797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408303 | GATGTGAAATTACTA[A/G]GAGAGAAACCCATGT | 10213 |
rs192159756 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313389 | GAGTCTTGCTGTGTC[A/G]CCCAGGCTGGAGTGC | 10213 |
rs192162455 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326103 | AGTGCAGTGGCATGA[C/T]CTTGGCTCATTGCAA | 10213 |
rs192181053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365061 | CAGTGAGCCAAGATC[A/G]CGCCATTGCACTCCA | 10213 |
rs192303062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337398 | TACCAAATGCCTTAC[A/G]TATGTTATCTCATTT | 10213 |
rs192317014 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377187 | CAGTATCCCACGACT[A/G]TCAGCTAGGGCTGGG | 10213 |
rs192397575 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310101 | GGTTGCAGTGAGCCA[A/G]GATCGCGCAACTGCA | 10213 |
rs192400957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381655 | AAATAAATAGCATAT[C/T]GGATGAACTGTATTC | 10213 |
rs192430751 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317156 | CGTTTTTAGCCTTTA[A/G]AAAGTGCTGTGTGTT | 10213 |
rs192436622 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341996 | TAATTTTTAAATGTC[A/G]CATTTTTGTTTGTGA | 10213 |
rs192529123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394687 | CAGTAAACAAGTAAA[C/T]AAAAATTTCAGGTCT | 10213 |
rs192564698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354356 | GCTCAAATGATCCTC[C/T]CACCTGAGCCCTCCA | 10213 |
rs192577771 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393815 | GACTTTAAGAAAAAC[C/T]GTCTTAAAATATAAA | 10213 |
rs192585298 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314994 | TGCCAAACTGTTCCC[A/C]GCACTCATTGGTTCT | 10213 |
rs192599965 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332335 | TTAAAACGTTTTCCT[C/T]ACAGTCCAGAAACTG | 10213 |
rs192603433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353592 | CTTGGAAAAGGTCTA[G/T]GTATTCCCTAATTCT | 10213 |
rs192607889 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372975 | AAGGAAAGTATAAAC[A/G]TAAACACAATGAAAG | 10213 |
rs192632619 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313975 | TATGTAACTGTCACC[A/T]CCATCCATATCCAGA | 10213 |
rs192683639 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400060 | GAGACTCCTATACTT[C/T]ATGTAACGCCTGAAT | 10213 |
rs192707909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357871 | AAGTTTAAGTTCCAT[A/C]ACATTCAATCTCCAA | 10213 |
rs192720933 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318383 | AGTTAATTAGCACAG[A/C]ACTTACTAATGAGGA | 10213 |
rs192749341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400173 | GAAAGGTATGTCTCA[C/T]ATTTCAAGTCCAATA | 10213 |
rs192776156 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326982 | TGAATCTGTGGATGA[C/G]AAACCTGTTGATATG | 10213 |
rs192827506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332934 | TGGCAAGTTTCTTTG[C/T]ACTTTCCCATTAATG | 10213 |
rs192834970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403586 | ACCGTGCTTTTAAAA[A/G]GCCTTTGATGACTGA | 10213 |
rs192839089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373262 | TATGAAATCATATGT[A/G]TCACTGTCTACTTTT | 10213 |
rs192897717 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372116 | CAACCACAGGGAGAG[G/T]GGATTAGAAAAACTA | 10213 |
rs192915355 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331799 | GAGCAGAGGAGAGCC[A/G]AAAGGACTGATGCTG | 10213 |
rs192952835 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161377917 | ATAGAGAAGAATACG[A/T]TCTACTCCCTGTCCT | 10213 |
rs192979439 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309340 | TAGTGACTGAAGGAA[A/T]AATTCTCGAGAAAAT | 10213 |
rs192986431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347167 | CCAAATTTTGGAGAT[C/T]GTTGTTCTTTGTTGC | 10213 |
rs193016936 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348609 | GAGGAATAATTCTAT[A/G]CGATTGTTTTTATGT | 10213 |
rs193024065 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389936 | GGTATTGCTATGTTG[C/T]CCAGGCTGGTCTTGA | 10213 |
rs193111628 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405510 | AGTGTAGATTAACTT[C/G]TTTATTGAGATGTTT | 10213 |
rs193118350 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352831 | GCAAGATACACACAA[A/G]CAGGAAGGTTATTTG | 10213 |
rs193142237 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323483 | GCCTGGCCAACATGG[G/T]GAAACCCCATCTCTA | 10213 |
rs193213242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366959 | TTTGTTGTTGTATAG[G/T]GGGAGGGGAACAGCT | 10213 |
rs193219877 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327582 | CCTCAAGATAGGAAA[C/G]CACAACTCAAAAGAT | 10213 |
rs193276522 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385176 | CAGTGAAAGCTGTTT[G/T]GTGTAAGTTTAGTAA | 10213 |
rs199538313 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161384547 | GCAAAATATAGAAAT[A/T]CTGTTACTTAGTATA | 10213 |
rs199631957 | in-del | -/TA | 0.0425829 | 0.139564 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350852 | CCTAAGGCAAAACCT[-/TA]GCAATCATATTGTAC | 10213 |
rs199633612 | snp | A/G | 0.000830576 | 0.0203617 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161395128 | AGGTTTGACACTTCA[A/G]GACTACAGTGAACAT | 10213 |
rs199712276 | in-del | -/A | 0.0221141 | 0.102801 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359482 | TTTTAATAAAAAGTT[-/A]TTTTTTTAAGGCAAA | 10213 |
rs199715093 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389958 | TGGTCTTGAACTCTT[-/G]GGCTTAAGTGATTCT | 10213 |
rs199747215 | in-del | -/AATT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339677 | ACGACCTATTGTATC[-/AATT]AATTAGATCCCAGCC | 10213 |
rs199786505 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312146 | CAGTCTGAAAAGTAA[-/T]TTTTTTTTTTTTTTT | 10213 |
rs199820892 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344114 | TTAGAGACTTGGTGC[-/G]GGGGGGGTGGGGAGC | 10213 |
rs199831521 | in-del | -/G | 0.0103295 | 0.0711199 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409143 | ACTAGGAACAAATTA[-/G]GACACTTGTATCCTG | 10213 |
rs199834490 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161340431 | GTGAGGGCAAAAGAG[G/T]GGGGACTGGAGTGAA | 10213 |
rs199837573 | in-del | -/AA | 0.0425829 | 0.139564 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350854 | TAAGGCAAAACCTGC[-/AA]AATCATATTGTACTT | 10213 |
rs199921946 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378226 | GATTAATAGATGTTT[G/T]CAGCCACTTTTCACT | 10213 |
rs200094141 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349992 | ATTTGTATTCTTTTC[A/G]TAAGAGGGAACTGGG | 10213 |
rs200100969 | in-del | -/TAAA | 0.0345262 | 0.126772 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310561 | ATGGGAGAACTTGAT[-/TAAA]TAATCTCTTCTAGTT | 10213 |
rs200166274 | in-del | -/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402710 | CAGGAAAAAAAAAAA[-/G]AAACTATAAAGAACT | 10213 |
rs200189923 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359140 | TGCCTGGCAAATCTT[G/T]AAAAAAAAATTTGTG | 10213 |
rs200203134 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344639 | ATTTCTGGTGTTCTT[C/T]TTTTTATTGTATAGA | 10213 |
rs200362732 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403580 | GTCACTACCGTGCTT[A/T]TAAAAAGCCTTTGAT | 10213 |
rs200378563 | snp | G/T | 0.000109631 | 0.00740294 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391083 | TTAATTTGTCCTTTT[G/T]AAAATCATTTATCTA | 10213 |
rs200438128 | snp | A/G | 0.000376494 | 0.0137152 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371356 | TTATTGCCATCTACT[A/G]CCACATTCTGTTTAC | 10213 |
rs200479688 | in-del | -/TA | 0.0425829 | 0.139564 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350853 | CTAAGGCAAAACCTG[-/TA]CAATCATATTGTACT | 10213 |
rs200532515 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161328031 | TAGATCTTTACCCGG[A/C]AAATAACAGACAATA | 10213 |
rs200554069 | in-del | -/AT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161341869 | TTAAAATTAAAAAAA[-/AT]ATATATATGTATATA | 10213 |
rs200560459 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392936 | TCAATTTTTCTTTCT[-/C]TTTTTTTTGGGGAGT | 10213 |
rs200572979 | in-del | -/TG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161341877 | TAAAAAAAATATATA[-/TG]TATATATAAATTTGT | 10213 |
rs200935721 | snp | C/T | 0.000802947 | 0.0200207 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408924 | ACTGTTAATAAGTTA[C/T]GCAGTTGCATAATAA | 10213 |
rs201112067 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359671 | ATACTAACTACTTTT[A/G]AATAGGAAGGACATC | 10213 |
rs201118450 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377575 | AATAATTTTACTTTT[A/T]AAATTCTAAGAGCAT | 10213 |
rs201130240 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161341223 | GCGCGGGCAGGCTCC[A/G]GGCTCGCGGCCGCCC | 10213 |
rs201192422 | snp | C/T | 0.000782963 | 0.0197704 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161370139 | AGTTGATCCAGTGTT[C/T]CAAGCTAAAATGTTG | 10213 |
rs201266313 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314707 | TAACTTGTAACATGT[A/G]CCAGTAAGTAGTACT | 10213 |
rs201362921 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161384334 | AGGGTGATTTTCTTT[C/G]TTTAAATCTTGTTCT | 10213 |
rs201454917 | in-del | -/TTAT | 0.0244538 | 0.107838 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344041 | TAAGTAATCTAGAGA[-/TTAT]TTAAAGTGTATGGAG | 10213 |
rs201522506 | snp | C/T | 1.69648e-05 | 0.00291241 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161411355 | TATGACCTCAAATAT[C/T]GTCCAGTGTTTAGCA | 10213 |
rs201537941 | snp | A/C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354785 | TTAGGCATTGTGCAC[A/C/T]GGGCTGCCAGCCCCT | 10213 |
rs201580850 | in-del | -/CA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388664 | AAGGATATCAGTTAC[-/CA]CACCGTATTTTCAGT | 10213 |
rs201611604 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331267 | TTTGGAATTTTTTTT[A/T]TTTTTTTATTTTTAA | 10213 |
rs201618752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317963 | AAAATTTGATTACTT[C/T]TTTTTGTTATTTAAG | 10213 |
rs201642231 | in-del | -/AC | 0.0111196 | 0.0737302 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309550 | ATAACAAAAACATGA[-/AC]ACAGTTTTAGTGGAG | 10213 |
rs201734509 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161341871 | TAAAATTAAAAAAAA[-/T]ATATATGTATATATA | 10213 |
rs201747223 | in-del | -/TTAA | 0.0138799 | 0.0821421 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313339 | ATACAAATTTTTATT[-/TTAA]TTAATTAATTAATTT | 10213 |
rs201780267 | in-del | -/TC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344638 | CATTTCTGGTGTTCT[-/TC]TTTTTATTGTATAGA | 10213 |
rs201840445 | in-del | -/TG | 0.44327 | 0.238052 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356046 | CTGTCAGCCAAAGGA[-/TG]TTTTTTTTTGGAACA | 10213 |
rs201842594 | in-del | -/GATA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161330093 | TTGATATGCAATTAT[-/GATA]AATAAATTTGTTCAA | 10213 |
rs201868306 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401778 | AAATCATGCATTTGA[C/T]ATTATTATTATTATT | 10213 |
rs202027670 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339894 | TAAATGAAAACATTT[C/T]CTATAAACTTACTGC | 10213 |
rs202065137 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339780 | GCCATGTGGCCTGTT[C/T]TCCCCTAAGCCCTGA | 10213 |
rs202102351 | snp | C/T | 3.51124e-05 | 0.00418986 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371150 | TTCTGTTCTGAGCAT[C/T]TGAATGCCCTCTTTG | 10213 |
rs202143519 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161374982 | TCTGTTCTCTGTTTT[G/T]AAAACATAAAAAAAG | 10213 |
rs202151340 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317134 | ATATACAGGATTCCC[C/T]CCGCCCCGTTTTTAG | 10213 |
rs202216505 | in-del | -/T | 0.483708 | 0.088773 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339497 | TATTTTGTTAATGAA[-/T]TTTTTTTTTTTTTTT | 10213 |
rs202245412 | snp | G/T | | | missense | PSMD14 | GRCh38.p7 | 2:161318854 | TTAGACTTGGAGGAG[G/T]TATGCCTGGACTGGG | 10213 |
rs367549589 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342171 | GACTAGAACCTTTAA[G/T]AAAATGTTAATAGAA | 10213 |
rs367553562 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372487 | AAATTGAGGTCTTCT[C/G]TAAATCATGATCCTA | 10213 |
rs367580053 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402315 | GAGAACGTTTTTGCA[A/G]ATCAGGTATCTGATA | 10213 |
rs367786613 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333165 | ATAAATTTCTGGAAA[G/T]AATTGTTGTATGTCT | 10213 |
rs367801983 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395576 | AGGGGATATAGATAA[C/T]AACAGCACTTACTAC | 10213 |
rs367815100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361702 | ATTTAATAGTGGGAA[A/G]TATTAATGTAATACA | 10213 |
rs367830421 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161381940 | ACCATGGTACTGAAA[A/T]CTGCACATCCCACAA | 10213 |
rs367837530 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161350414 | TATACCAAGAAGGAA[A/G]TTAACTAGTCCTAAA | 10213 |
rs367921679 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161356055 | AAGGATGTTTTTTTT[-/T]GGAACATTTTTTTTT | 10213 |
rs368053450 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359491 | AAAGTTATTTTTTTA[A/G]GGCAAAGATTTTTTT | 10213 |
rs368059742 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339617 | CTATAAGCCAGGGTC[A/G]GAAACTTTCCAGACA | 10213 |
rs368076605 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326552 | CAATTCAGCTTCTGG[A/G]TATGTGCCCAAAATA | 10213 |
rs368096782 | snp | A/G | 9.05647e-05 | 0.00672861 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161395098 | GCTAAATTTGCATAA[A/G]AAGAGTTGGATGGAA | 10213 |
rs368192340 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161362820 | CTAAGATTTCTCAAG[A/T]TACAGTTTTTTATTC | 10213 |
rs368223700 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335677 | ACAAACCGTGTTGTA[A/G]TAAATATCTCATTGA | 10213 |
rs368236523 | snp | C/T | 0.000169985 | 0.00921758 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395252 | TCTTTGGAATATGTA[C/T]GATTAGATGCCAAGC | 10213 |
rs368267250 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348873 | TTGTATTTCCTAAAT[A/G]TTTCATAATAAATTT | 10213 |
rs368270283 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378203 | GATTTTTAGGCTACT[A/C]GTAAGCTGATTAATA | 10213 |
rs368488419 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402134 | TTAATCTGCCTCTTC[A/G]CATTGCCAGTTCCAC | 10213 |
rs368565378 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349092 | CAGTCCGCTGCCGAA[C/T]TGGCTTACTATAGGT | 10213 |
rs368571075 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400511 | TTTTTGAGATGTACA[A/G]CAATTTGAAAAAAAC | 10213 |
rs368586876 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161379489 | AAATATATCTTAAAG[C/T]GTCACTCTCTAATTT | 10213 |
rs368589500 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352685 | TTCACCCATTTTTTT[-/T]GGATTCCCTCTCCTC | 10213 |
rs368633825 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371948 | GTTCTCTTTCTCTTT[G/T]TTTGTTCATTCATTC | 10213 |
rs368709958 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331357 | AACCTCCGCCTCCCA[G/T]GTTCAAGCGGTTCTC | 10213 |
rs368752667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326212 | ATTTTTGTAGTTTTA[A/G]TAGAGACAGGGTTTC | 10213 |
rs368805545 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323475 | CAGGACCAGCCTGGC[C/T]AACATGGGGAAACCC | 10213 |
rs368967654 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336657 | CTTGGCTCACTGCAA[C/T]CTCTGCCTCCTAGGT | 10213 |
rs368973927 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365863 | AACTGTAGTCACCAG[A/G]CTATGCAGTAGATCA | 10213 |
rs368998914 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358828 | TACCTGTAATCCCAG[C/G]TACTTGGGAGGCTGA | 10213 |
rs369036021 | snp | A/G | 0.00069138 | 0.0185799 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367738 | AAAGAAGAACCAGAG[A/G]CCTCAACGAAATTTG | 10213 |
rs369128260 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330810 | GCTTAGGGACAATAG[A/G]GTAAATAATAAAAAT | 10213 |
rs369134511 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161351993 | CTGATTAGTCTCTCT[A/G]CTTCATATATCTATG | 10213 |
rs369144442 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352693 | ATTTTTTTGGATTCC[C/T]TCTCCTCTGTGTGGT | 10213 |
rs369147459 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393674 | TAATGGTTCTATTGA[C/T]GAAACAACAGTCATT | 10213 |
rs369299021 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386466 | ACACTTTGATAACTT[C/T]ATACTTTTAAATGCT | 10213 |
rs369301146 | snp | A/T | 0.000169986 | 0.00921759 | intron-variant | PSMD14 | GRCh38.p7 | 2:161411275 | AATATGGTTCTGTTT[A/T]CTCTTTCCTCATTTT | 10213 |
rs369312610 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402686 | AAGAAAGTATACAAG[A/T]ATTAAAAACAGGAAA | 10213 |
rs369327957 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353885 | CATACATGGCTTTGC[-/A]TATTATAATTTAGAA | 10213 |
rs369361661 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314308 | TTTCTTGTTGAATAA[A/G]TAACTGAGTAAGAAT | 10213 |
rs369384253 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320972 | CTCAAGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 10213 |
rs369478343 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352917 | CAGCTGATCACAGTA[G/T]CATCCACTTAACCTT | 10213 |
rs369651682 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391737 | GCTGGGACTATAGGC[A/G]TGCACCACCACACCT | 10213 |
rs369674882 | in-del | -/TGTG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161327946 | AATTCTCATGTAAGC[-/TGTG]TGTGTGTGTGTGTGT | 10213 |
rs369676912 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324931 | GCTTTAAGAATCAGT[G/T]TGTGATTTGTCTGCC | 10213 |
rs369681066 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375409 | TATATGCCAGTATAC[A/G]ATAAAGTATTACTTG | 10213 |
rs369734569 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404028 | CTCTTGCCTCAGCCT[C/T]CTGAGTAGCTAGGAC | 10213 |
rs369761392 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395472 | GGGCTATAGTTTGCC[A/G]ACTCCTGTTGTAGAC | 10213 |
rs369976132 | snp | C/G | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306579 | GCTTCTGTAGTGCCT[C/G]AAGGTCACCCAGAGG | 10213 |
rs369993189 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383662 | TTTCATAATTTTGTA[-/G]TAGCTTTTTCTCCCT | 10213 |
rs370012266 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382879 | CCCTACCAACCCATA[-/A]CATTAATTAATTCTT | 10213 |
rs370032297 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161351736 | ACATGGGTCGTCTGG[A/G]TGCTCTGTTCCGTGG | 10213 |
rs370034988 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375964 | GTGTCTTTTCTTTCA[A/G]GGGTGGGTAGCAAAT | 10213 |
rs370039466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404605 | TGCCTCCAGTATTCT[C/T]GGAGTCATAACCTTT | 10213 |
rs370043462 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346609 | TTAGAAATATTCTTG[A/G]TATTTGTTATGGGAT | 10213 |
rs370082078 | snp | C/T | 2.11674e-05 | 0.00325319 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161408887 | GCTGGCAATAAAGAA[C/T]GTTGGCAAGCAGGTG | 10213 |
rs370104562 | in-del | -/G | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307454 | ATAGGTTTGGGGGGG[-/G]AAGCATAAAGATGTG | 10213 |
rs370107478 | snp | C/T | 0.000161076 | 0.00897285 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395061 | GAAAAAGAATTACTT[C/T]TTCTTTTATTTTTTA | 10213 |
rs370160365 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338842 | CCCCAGACTACCACT[A/G]ATTTGCTGTCACTAT | 10213 |
rs370163163 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369831 | GTTATGGTTGGTTCA[A/G]TTATTTCGTATTTCT | 10213 |
rs370264007 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315493 | ACTGAAAAAAAGACT[A/G]CAGAGATGAAGTCTC | 10213 |
rs370354697 | snp | C/T | 0.0001033 | 0.00718607 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391096 | TTTAAAATCATTTAT[C/T]TATATAGGCATTAAT | 10213 |
rs370372256 | in-del | -/G | 0.375 | 0.216506 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356047 | TGTCAGCCAAAGGAT[-/G]TTTTTTTTGGAACAT | 10213 |
rs370453229 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377284 | TAGGAAATCGAATAC[A/G]TAAAGAAATCTATTT | 10213 |
rs370564892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323196 | ATTTTTTAAACTGCC[A/C]AGTCTATTGGCCTAT | 10213 |
rs370663872 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345799 | ATATTTATATTTTTT[-/T]CTGCTTATAATTGTA | 10213 |
rs370714394 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405005 | CTCCACTGTCTGAGA[A/C]CTTTCCAGTTACATG | 10213 |
rs370721942 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339748 | TCTGTGTTGAAGGCA[A/G]TGACTGTGTGGCTGT | 10213 |
rs370880385 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324347 | CTCATTGTAAATAAC[A/G]TGATTTGTAAGTACA | 10213 |
rs370890741 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388642 | GCTTCATTTTAGAAC[A/G]TGATTTAAAGGATAT | 10213 |
rs370960899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337804 | GGATCAGGAGATAAG[C/G]GTTCTGGTTCTCAGT | 10213 |
rs370975826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349018 | CTCACTCCCAGAGAG[A/G]CATCTTTCTATCTTA | 10213 |
rs370984071 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161316661 | TTTTAACAGATGTCA[A/G]ATTATGAATGTGATT | 10213 |
rs371004429 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312020 | ACTGGAAAAAAGTCC[G/T]TAAGAAAGTGAGAAT | 10213 |
rs371004523 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161407024 | TGGTATTTTGAGCCA[A/G]ATTCCAAAATTTTTG | 10213 |
rs371043517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325284 | TGAGATATAGTGTAC[A/C]TTTTGAAGAATTATT | 10213 |
rs371089587 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368194 | TTACTTACCCTATAA[C/T]AGCAGAGTGTTAGTT | 10213 |
rs371214788 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394191 | TAACCAGGCTGGTCT[C/T]GAATTCCTGACCTCA | 10213 |
rs371311842 | snp | A/G | 1.70778e-05 | 0.00292209 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161385538 | AAGACAAACAACTTC[A/G]AATCTGGGTCACTTA | 10213 |
rs371323803 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326327 | AGAGCCACCATGCCC[A/G]GTCCAAACTTCATAA | 10213 |
rs371427474 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323974 | GCATCTAAACGATTT[C/T]CAAAAGCAGTGGAAA | 10213 |
rs371449473 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400345 | CAGGAAGAGAAGAAA[C/G]GGCAAAAGGGGGATA | 10213 |
rs371601196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333892 | AAAAATTAGCCAGGC[A/T]TGGTGGCATGCACCT | 10213 |
rs371663038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342255 | ATCTGACCATCAAAC[A/G]TGATATTAGCTGTAC | 10213 |
rs371698952 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360709 | CCTAGCTAATTTTTT[-/T]GTATTTTTAGTAGAG | 10213 |
rs371701461 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382362 | AAATAGGCAGCATTA[C/T]ATGAACAAAATTTAT | 10213 |
rs371704673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391413 | GTAGGAAATAAATCA[A/G]ACGTTCCACTTTGGT | 10213 |
rs371726375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360504 | GGATTATAGGTACCC[A/G]CCACCATGCCTGGCT | 10213 |
rs371781854 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314761 | GTATTTCATATTACA[A/G]TATTCCTATATGTGT | 10213 |
rs371805533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358667 | TTAAAGAGCCTGGCC[A/G]GGCACGGTGGCTCAC | 10213 |
rs371834206 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404082 | GGCTATTTTTTTTTT[-/T]CTTTTAAGATACAAA | 10213 |
rs371867136 | in-del | -/A | 0.0138799 | 0.0821421 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309394 | ATATTATGGAAAGGC[-/A]GGGGAAAGGGTTTAA | 10213 |
rs371889810 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362739 | TTGCATTTTTTTCCC[A/G]GCAGGCTGTTTGGTT | 10213 |
rs371994589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340680 | GATTGAGGGTCTAGA[A/G]CTCAGCAGATTTATG | 10213 |
rs372004530 | snp | C/G | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306414 | CTCCCAGTCTTTCCT[C/G]AGGGGTTTAGTACTT | 10213 |
rs372069603 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161350673 | AAAACAAAATTAACT[A/G]AATTGAGGAATAAGT | 10213 |
rs372137808 | snp | A/T | 0.000167986 | 0.00916322 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318886 | CAGGTTAGTATATAG[A/T]CTCTTGAGCATTTCC | 10213 |
rs372285099 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392196 | CCCTTTACTATTACA[A/G]TTAGTCATCCACCTA | 10213 |
rs372405555 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398240 | TGGGTTTTTTTAGTA[A/T]CACTTAAAATATAAA | 10213 |
rs372471479 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396689 | AGACATAGGACATGT[G/T]TAAGAAACAATATGC | 10213 |
rs372482025 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394554 | ATTAATTCATTCATT[-/C]ATCAGATATTTATTG | 10213 |
rs372571937 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395747 | CACATTTATACATTA[C/T]GCAGTGTTATATTAA | 10213 |
rs372582445 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404774 | TTGAACTTCTGAAGT[A/C]TCTTTTTACTTCCAT | 10213 |
rs372628875 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313103 | GCAGATGAGGAAACT[A/G]AGGAGGAGAGAGGTA | 10213 |
rs372663547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376458 | AATAGAATGTGAATG[C/T]TTCTGCAAGTTTTGA | 10213 |
rs372671401 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326134 | CCTCCACCTCCTGGA[C/T]TCAAGAGATTCTTCT | 10213 |
rs372709404 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371998 | TCTTTCTTTCTAGCC[C/T]CATATGCCATTTTCC | 10213 |
rs372713858 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377607 | GTCGTATATAGAGGT[-/T]AAGAGTTCCTATGGA | 10213 |
rs372716075 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312944 | AGGATCTGTGTTGGT[A/G]GCCATGCTCAGGATG | 10213 |
rs372731375 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161387442 | CTTGCTCCTAAACCA[A/G]CTTTCAAGTAGTAGG | 10213 |
rs372838044 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365651 | ATGAATACAGTGTTC[A/G]TTAACCTATTTTTCT | 10213 |
rs372853502 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161379522 | TATTTTTTATGTGTC[A/G]GGTGTCTCTTGATGT | 10213 |
rs372856329 | snp | A/C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307363 | AAGTGTTCATACTCT[A/C/T]AAGTTTCTGATTAGG | 10213 |
rs372942616 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343879 | AGTTCTTTTGGGTAT[A/G]TAGGTAGCCCTCCTT | 10213 |
rs373137894 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346766 | CTCTTCTAATTTTGT[A/G]AATTCTGAAATTTTC | 10213 |
rs373159775 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321089 | CTATCTTTTCATTAG[A/G]TAAGGCATAGGCACC | 10213 |
rs373164724 | snp | A/G | 5.7538e-05 | 0.00536336 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161371271 | CTTTGAAGCCTTGTC[A/G]GAGAGAGCTGTGGCA | 10213 |
rs373192763 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161309993 | GTGAAAACCCGTCTC[C/T]ACTAAAAGTATAAAA | 10213 |
rs373195827 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380403 | ACCATACTAGTTTCT[A/G]AAGATCGATTTGTTT | 10213 |
rs373205422 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333808 | GAGGCCAAGGCAGGC[A/G]GATCACCAGGTCAGG | 10213 |
rs373208318 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368516 | GTTTGTTTTGTTTTG[A/C]CTTTTTGTTTGATGC | 10213 |
rs373238599 | snp | A/G | 0.000231367 | 0.0107531 | intron-variant | PSMD14 | GRCh38.p7 | 2:161411258 | GTAATTTATCTACCA[A/G]TAATATGGTTCTGTT | 10213 |
rs373283312 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404150 | GCCTCAAGTGATGCT[A/T]CCCCCTCAGCCTCCT | 10213 |
rs373289616 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360165 | AAACAGCTTTTTTCC[A/C]CCCCGTAACATATAT | 10213 |
rs373304404 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358895 | GGCATAGCCATCTAG[C/T]ACATGAAGTATCTTG | 10213 |
rs373421994 | snp | C/G/T | 0.00637447 | 0.0561625 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314666 | GCCTGGCTTCTTTTA[C/G/T]ATAGTGTGATGTTTT | 10213 |
rs373448802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343848 | AAAAAAAAAATGTCT[C/T]TGAGTCTCTGCTTTT | 10213 |
rs373474779 | in-del | -/CT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161384548 | AAAATATAGAAAYWC[-/CT]TSTTACTTAGTATAT | 10213 |
rs373495436 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323593 | ACTTGAACCCAGGAG[A/G]TGGAGGTTGCAGTGA | 10213 |
rs373498377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399195 | AACCATGTTTCCAAA[G/T]GGGAAGACTTAGTAT | 10213 |
rs373562699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410222 | CTCAGTGTTTTTCAC[C/T]TAAAATGCCCTAAGA | 10213 |
rs373671233 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161361067 | GAGTTTCTACCTAAA[A/G]TGTGCTTCTTCACCC | 10213 |
rs373789654 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332323 | TTTTTTACGTCTTTA[A/G]AACGTTTTCCTTACA | 10213 |
rs373859105 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339274 | CAGTGTGTGAGAGTT[C/G]CCGTTCTTCCACATC | 10213 |
rs373893924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370321 | TAAATATCAGTGCCA[C/T]GCACCACCTGTCTAG | 10213 |
rs373947760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393835 | TAAAATATAAACTTG[A/G]AAACTTAGGAACATC | 10213 |
rs374029231 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322754 | CAGTATTATAATCAC[A/G]GTTGATACTGATATT | 10213 |
rs374126869 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311346 | ATCTATATTGAACAT[A/G]TATAGACATTTTTTT | 10213 |
rs374129338 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396930 | TCTCCTGTGTTCAAG[A/T]GATTCTCCTGCCTCA | 10213 |
rs374209295 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371515 | TTTATTTAGAGATTT[A/C]TTCTTTAATCACTTA | 10213 |
rs374219409 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312691 | TATCATGAATGAGCT[C/T]TTGAGTCTTCTACTT | 10213 |
rs374221229 | snp | C/G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411663 | TATTTGAAAAAATCA[C/G/T]TAGCACAAATATATT | 10213 |
rs374246570 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386394 | ACCTTGCTCTGTCAT[-/T]GAGGTTGTCTTTGGG | 10213 |
rs374315217 | snp | A/G | 8.94015e-05 | 0.00668526 | missense | PSMD14 | GRCh38.p7 | 2:161391140 | AGACATTATTACTCC[A/G]TTACTATTAACTATC | 10213 |
rs374338464 | snp | A/T | 0.000169986 | 0.00921758 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395246 | TTATAATCTTTGGAA[A/T]ATGTATGATTAGATG | 10213 |
rs374600740 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310562 | TGGGAGAACTTGATT[A/G]AATAATCTCTTCTAG | 10213 |
rs374636143 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309508 | GTGTTTGAGAAAAGC[-/A]GCAAGACATGCACTG | 10213 |
rs374731297 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161355078 | GATATAGAGTATGGT[A/T]TAGGAATATAGTATA | 10213 |
rs374769249 | snp | C/G | 5.51354e-05 | 0.00525021 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318913 | TTCCTTGTGTGTAAA[C/G]TACAAGCCTTTTTGT | 10213 |
rs374871948 | snp | A/G | 9.64488e-05 | 0.00694371 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318796 | TTTGTGCTTAGGAAC[A/G]TTTTTTCTTTGTTTC | 10213 |
rs374890305 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161379964 | ACCTGGTGTGAATGC[C/T]CAGTAGAGCCAAAGG | 10213 |
rs374903621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324876 | GATTTTGCTTTGACC[A/G]ATGGAATGTGATTGG | 10213 |
rs375041187 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320278 | ACTTTCCTTAAGCAT[A/G]GATACAATAAATTAC | 10213 |
rs375131012 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391611 | GTTTGTTTTAAGAGA[C/T]AGTAGGGTCTTGCTC | 10213 |
rs375132479 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314671 | GCTTCTTTTACATAG[A/T]GTGATGTTTTGAGGT | 10213 |
rs375160330 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342717 | GTCGTTAAGTTTAAA[G/T]CTTTCATTTTGCTGT | 10213 |
rs375194341 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402590 | AGGCTGCAATGAACC[A/G]TGATCATACCACTGT | 10213 |
rs375265749 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408636 | GTGTATTTCTTGTCT[C/G]TTTTCAAAATGATGA | 10213 |
rs375373728 | in-del | -/TGT | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366997 | GTGACATGCAGAGGA[-/TGT]TGTTCACAGCTCTTT | 10213 |
rs375498328 | snp | C/G | 2.75327e-05 | 0.0037102 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408811 | ATTTATAATTTTAAA[C/G]TCTGTCCTTTGTGTT | 10213 |
rs375526233 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375200 | GAATTTTAAAAAATG[A/G]TCTTTGTGTTCTTTG | 10213 |
rs375579236 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388808 | TATAATCCGTAAGCC[A/G]TGTGTTTTATAATGC | 10213 |
rs375652746 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326267 | AACTTCTGACCTCAA[A/T]TGATCCGCCCACCTC | 10213 |
rs375663445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310787 | AGGTGGTGACGCCGG[A/T]TTCAAATTGAGGTCA | 10213 |
rs375696176 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389438 | GCCCTGATCATTTCT[A/C]CTTTTTGATCTGTAC | 10213 |
rs375728637 | snp | C/G/T | 0.000223563 | 0.0105707 | intron-variant | PSMD14 | GRCh38.p7 | 2:161411273 | GTAATATGGTTCTGT[C/G/T]TTCTCTTTCCTCATT | 10213 |
rs375731865 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352711 | TCCTCTGTGTGGTGC[G/T]TTCTTTTTCTTGTAT | 10213 |
rs375749380 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324711 | TGATCTGTGTTTTTG[A/G]AAAGTAATTCTAGTG | 10213 |
rs375765245 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335821 | AATTTAGGCTTTACT[A/G]CTTAGTCACTTTTTA | 10213 |
rs375787400 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161350395 | ATGAAGAACTTCAGT[A/G]ATTTATACCAAGAAG | 10213 |
rs375886173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325302 | TTGAAGAATTATTTC[C/T]GGTGGCTAGATAAAA | 10213 |
rs375929917 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349089 | GCTCAGTCCGCTGCC[A/G]AATTGGCTTACTATA | 10213 |
rs375972989 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161379433 | AATAACCTTCAGTAC[A/C]ACTATACACTTTCTT | 10213 |
rs376034607 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373200 | AATATGTATGTGTCA[C/T]GTCTTAATGTTAAAT | 10213 |
rs376108039 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314596 | CTGCATTCTGTCTCT[A/G]TGGATTTATTGGATA | 10213 |
rs376137497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386381 | TGCTCCCTTCTGAAA[A/C]CTTGCTCTGTCATGA | 10213 |
rs376150770 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382710 | TAGCTCAGAGGTTTT[C/T]GTTATTATATATTAA | 10213 |
rs376217922 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310206 | GGTTCATCTTATTTT[-/T]CATACTGGCCATGTA | 10213 |
rs376279857 | snp | A/C | 0.000169986 | 0.00921759 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385578 | TCTATCCAGGTATTG[A/C]CTATATTTGATAATG | 10213 |
rs376381160 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310034 | GGCATGGTGGCACGT[A/G]CCTGTATTCCCAGCT | 10213 |
rs376401784 | in-del | -/AGAG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161387915 | TAATAATCCTGATAG[-/AGAG]GAGAAAGTATAATGC | 10213 |
rs376439820 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344403 | TCGCATAGCAGAAAG[A/C]AAGCTAAGAGTTTTC | 10213 |
rs376452471 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346322 | CACCCCCTGCTTTAT[C/T]CTATTGCTAGTGGTA | 10213 |
rs376459726 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375641 | CACAGATATTAGAAT[A/G]TAAAATGAGTGCTTT | 10213 |
rs376506893 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365814 | AGAACATTTAAAGTC[A/G]TCTTTTAACTATTTT | 10213 |
rs376514653 | snp | C/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307487 | TCCAAATATTACCTA[C/T]GAGTAAAATAATCTT | 10213 |
rs376518418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336489 | TTTTCAGTGATGTTA[C/T]TTATTTGAAACCCTT | 10213 |
rs376527510 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309463 | TTGTTCCACTGGTCA[C/T]AAGTGTTTTTTTAGT | 10213 |
rs376542846 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398387 | ATAATTAAATTCTTA[C/T]GTCCCAAGTTTTCAG | 10213 |
rs376550815 | snp | A/G | | | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161411839 | TACAACACATAAAAC[A/G]TCAGTGTGATAAAAC | 10213 |
rs376630767 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306536 | TGCACCAACCAACCA[A/G]ATAATTCTGCCTTAG | 10213 |
rs376640652 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364529 | GGCCCCCCTCCCCTC[A/G]TATCAGCTGTTCATG | 10213 |
rs376664682 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344642 | TCTGGTGTTCTTCTT[A/T]TTATTGTATAGATCC | 10213 |
rs376720455 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161330941 | CCTAGTGTTGTAAAC[A/G]GAGCCTGAGTTATTA | 10213 |
rs376741890 | in-del | -/ATA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333137 | AAAATTTGTTTAATA[-/ATA]GCATAGAAATATAAA | 10213 |
rs376796345 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400247 | CTGCTCTGCTTTCCT[C/T]GTGTTGGCTTTCTTC | 10213 |
rs376846534 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382598 | AATTAAATGGTCAGG[C/T]GGGTGAATAGAGATT | 10213 |
rs376892941 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337765 | TTGAGATGATGTGCT[A/G]TAGCAGGAAGGGGAT | 10213 |
rs376967071 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161351786 | AAGCTGATACAGCGC[C/T]ATCATTGAACACTGA | 10213 |
rs376995488 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359507 | GGCAAAGATTTTTTT[C/T]TTAATTGGACTTGGA | 10213 |
rs377046567 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376843 | ATAGTTTTTTAATAA[A/C]TGTTTATAAAATAAA | 10213 |
rs377129712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315929 | GCTCATTGCAATCCA[C/T]CTCTGGGGTTCAAGC | 10213 |
rs377163286 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311806 | TTTTAGTAGAGACCA[A/G]GTTTCGCCATGTTGG | 10213 |
rs377246344 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402287 | AAAAGAGAAAAGACA[A/G]CCTACAAAGTGGGAG | 10213 |
rs377307742 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161341062 | CTTCGGGCTCCCCCG[A/G]TCCCGCAGGCTCCCC | 10213 |
rs377310488 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161341670 | CGGTGAAACCCCATC[C/T]CTACTAAAAATACAA | 10213 |
rs377313615 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372153 | TACAGAAATTGGCTA[A/G]GTGGTTACTGCTTTA | 10213 |
rs377321450 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359398 | GCCTGGTTTTTATTT[C/T]TCTATCATTTGTGTG | 10213 |
rs377443841 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393415 | GTCCTTACCCCTGGA[A/G]CCATGGGAGAAAATG | 10213 |
rs377512708 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331323 | GCTAGAGTGCGGTGG[C/T]GCGATCTCGGCTCAG | 10213 |
rs377513600 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350292 | AAGTATGTCCCAAAT[-/A]CAGCCTGGGATGTAC | 10213 |
rs377532352 | snp | C/T | 0.000351825 | 0.0132585 | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411406 | ATTTAAATAAAGCAA[C/T]GAAAAACGCTATTAA | 10213 |
rs377566606 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352452 | ACCAAGACTTACTCT[C/T]TTTCCTTTTATTTTG | 10213 |
rs377570868 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387735 | TGGATGGTAGAATTA[C/T]GAGATTTTTTTGTCT | 10213 |
rs377575826 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323610 | GGAGGTTGCAGTGAG[C/T]CAAGGTAGTACCACT | 10213 |
rs377668692 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161353779 | CCTACTTGTGTGTAG[C/T]TAGTACATGGTATGT | 10213 |
rs377677217 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320563 | CTCTTATTTTTATGG[C/T]ATCTCCCTTATCCTA | 10213 |
rs377710223 | snp | A/G | 0.000187982 | 0.00969307 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391070 | TAGGTGAAAAATATT[A/G]ATTTGTCCTTTTTAA | 10213 |
rs386391660 | in-del | -/TTTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357085 | AATGCCTTTTTTTTT[-/TTTT]TTTAGCACTTAGTCA | 10213 |
rs386652135 | multinucleotide-polymorphism | AT/GC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161330098 | ATGCAATTATGATAA[AT/GC]AAATTTGTTCAAGTT | 10213 |
rs386652136 | in-del | AC/GCT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342332 | TCCTACTTTGTTGAG[AC/GCT]TTTTTTTTTTTATCA | 10213 |
rs386652137 | in-del | C/TTTGT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348928 | TGGTTAGAAAAAACA[C/TTTGT]TCCTACTCCAGGTAG | 10213 |
rs397731806 | in-del | -/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367687 | ATAAAAGGAGTTTTT[-/T]ATTTTCACTGGAACA | 10213 |
rs397744603 | in-del | -/AA | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343841 | TCAAAAAAAAAAAAA[-/AA]TGTCTTTGAGTCTCT | 10213 |
rs397749800 | in-del | -/A | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402709 | ACAGGAAAAAAAAAA[-/A]GAAACTATAAAGAAC | 10213 |
rs397779981 | in-del | -/T | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357915 | TTCTTTTTTTTTTTT[-/T]AATGGTGGTGAAACA | 10213 |
rs397783865 | in-del | -/CT | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384549 | AAATATAGAAATACT[-/CT]GTTACTTAGTATATG | 10213 |
rs397808767 | in-del | -/A | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323942 | TTGTCTTTATAACAA[-/A]CTCCACCTAGGTCTT | 10213 |
rs397830547 | in-del | -/ATT | 0.5 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401796 | ATTATTATTATTATT[-/ATT]CAGGTTGTATCAGTG | 10213 |
rs397842803 | in-del | -/ACACAC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366412 | cacacacacacacac[-/ACACAC]acacaAAAGCACAAA | 10213 |
rs397870635 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342344 | AGACTTTTTTTTTTT[-/T]ATCAGAAGTGGATCT | 10213 |
rs397871757 | in-del | -/TT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338357 | TTTTTTTTTTTTTTT[-/TT]GGAAAGAAAAACTTC | 10213 |
rs398080770 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402708 | AACAGGAAAAAAAAA[-/A]AGAAACTATAAAGAA | 10213 |
rs527287619 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309473 | GGTCACAAGTGTTTT[G/T]TTAGTGCTTCTGACT | 10213 |
rs527288801 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411507 | GGCTAAATGTAAGAC[A/G]TCTGGCATCATTTGC | 10213 |
rs527379912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348429 | GCTGGTTTGCCGATA[A/G]GTTGTAGTTTGGAGA | 10213 |
rs527389655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394137 | CCACCACACCCAGCT[A/C]ATTTTTGTGTTTTTA | 10213 |
rs527393449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403665 | GCCTCTGTTGCTTTA[C/T]TTCTTATCACTGTTG | 10213 |
rs527417525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349209 | GTTGTTTTATAAGTA[C/T]GCGTCAAATCCTAAT | 10213 |
rs527419682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340625 | CACAGGGCAGGGCCA[A/G]AGGTGTTCTCAGGAT | 10213 |
rs527460693 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316095 | GTGATCCGCCCGCGT[C/T]GGCCTCCCAAAGTGC | 10213 |
rs527574982 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364303 | CTGCTTATGTGTTCT[C/G]TTCCTCTCAATGTCC | 10213 |
rs527611868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364961 | TACAAAAAATCAGCC[G/T]GGCGTGGTGACATGC | 10213 |
rs527623037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161308812 | CGCCTCCTTTCTCCA[C/T]TCTTTTCTGTTTGGC | 10213 |
rs527625459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316897 | TCATATATATTCACA[A/G]CATCTGGAGTCTGTG | 10213 |
rs527640830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376699 | TTGAAACTTGGGCCT[A/G]TGAGGTGATTAATGT | 10213 |
rs527693260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318139 | AATTGAGAAGCACAG[C/T]TGAATTTCCTTAGTG | 10213 |
rs527752360 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323682 | AAAAAAAAAGTTAAT[A/G]TTTGAATAGTGATAG | 10213 |
rs527820139 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311469 | TAGGAGGATGTGCAT[A/G]GGTTATATGCAAATA | 10213 |
rs527884221 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321393 | AATCATGATCTATAC[A/G]AATAACCCAATTTTG | 10213 |
rs527891331 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358258 | TTTTTAGTCCTATAA[A/C]TAGGACATGTATAAT | 10213 |
rs527892948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333781 | CTCACGCCTGTAATC[C/G]CAGCACTTTGGGAGG | 10213 |
rs527908353 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323198 | TTTTTAAACTGCCAA[-/G]TCTATTGGCCTATTT | 10213 |
rs527925676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394746 | GGTTAAGGGAAGAAA[A/G]ATTTTGTTTAAGGTA | 10213 |
rs527957959 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386499 | ATTTTGGGGCAGTCA[C/G]TCATCTGTAATCTTC | 10213 |
rs527966296 | snp | C/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307763 | TCTTCTGCAACTTTG[C/T]TTTTTGAAAGCCTAG | 10213 |
rs527973360 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396271 | ATCCCGCAATCCCAC[C/T]ACTGGTTGCACATCC | 10213 |
rs528006381 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387672 | CAAGTGTATATTTTA[C/T]AGATGGTGCCTATAT | 10213 |
rs528084951 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397546 | TTAATGGTAAAGGCT[A/G]GAGCTCAAGATTTCA | 10213 |
rs528096210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323146 | TCACTCACATGAGAA[G/T]GCATTCTGGCCAACT | 10213 |
rs528096563 | in-del | -/T | 0.02016 | 0.0983543 | intron-variant | PSMD14 | GRCh38.p7 | 2:161398539 | GAGATGCATCTGCTA[-/T]TTTTTTTTAATTTTG | 10213 |
rs528139638 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161309127 | GAATATCTTAAAAAC[A/G]AAGTGTGCTACTATG | 10213 |
rs528157033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361368 | GAATTTATCAATACA[A/G]CTGAAAAGATTATAA | 10213 |
rs528216641 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306432 | GGGTTTAGTACTTAC[A/G]TTGGGACAAGCCTTC | 10213 |
rs528251256 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371142 | ATTACTTGTTCTGTT[C/T]TGAGCATCTGAATGC | 10213 |
rs528265204 | in-del | -/GAG | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331717 | GTATGGATCTATAAA[-/GAG]AACCCACATATTTTG | 10213 |
rs528270123 | snp | A/G/T | 0.00159649 | 0.0282165 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345148 | TTTCCTCATTTAATT[A/G/T]TCTTGGTCCCTTTGT | 10213 |
rs528276729 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343004 | GGACCTTTGTGCTAT[A/G]TGTTGAAAATCCATG | 10213 |
rs528296477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337029 | GAAGTAACTTATTCA[A/G]AGTCATTTAAAGAAA | 10213 |
rs528318849 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399619 | TTTTAAAATAAGTTG[A/C]GCAAAAGAGAAAACT | 10213 |
rs528364129 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390250 | AGTTTTTCTCTTTAG[A/T]TTCCTGAGGGTTAAC | 10213 |
rs528377857 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408481 | GAAAAGGAGAGAGCA[A/G]CAGAACAGAATTAGT | 10213 |
rs528380846 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378358 | AACTCAGAACTGAGC[-/A]GTGATAAGTAAAGAC | 10213 |
rs528401756 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379925 | TGTTCAGTTGTTGGC[A/C]GGGAGCTGCCCAGGA | 10213 |
rs528456601 | snp | A/G | | | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411717 | ATACATTTACAGTCT[A/G]TGCCTCCTGAGATCT | 10213 |
rs528462310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338869 | CTATACATTAGTTTG[C/T]ATTTTCTAGCATGTT | 10213 |
rs528478339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339671 | GGAGTCAACGACCTA[G/T]TGTATCAATTAGATC | 10213 |
rs528488246 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345793 | CCAAAGATATTTATA[-/T]TTTTTTCTGCTTATA | 10213 |
rs528496879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331923 | TATAGGGTCGAGTCA[C/T]AGAACTAACAAGAAG | 10213 |
rs528521427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401867 | AGGTCTTTGGAGATA[C/T]ATAGGACTGTGTTTA | 10213 |
rs528532626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392062 | TGACGTTTTGATGAA[G/T]TAGCATTCTCATTTG | 10213 |
rs528559858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392792 | ACACTTATTTTTAAG[G/T]TTACATGGAATGAGT | 10213 |
rs528582431 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383718 | TGAAATGGGCCAAAA[C/T]GATGCTTTGCTCCTA | 10213 |
rs528588800 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345892 | TCAAGTTCATTCTTT[A/T]TATTTTTATTTTTTC | 10213 |
rs528620403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354471 | GCTGCTGAATGATGT[G/T]TTTTTATAACAAAGG | 10213 |
rs528636944 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362928 | CTTTGTTTATTGTTT[C/G]TGTTTATTTTAGCCT | 10213 |
rs528643330 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161308003 | GGTCCCCTCTAATCA[C/T]ACCATCCCCCCTCTT | 10213 |
rs528644431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324512 | GATACATAAGAAAAT[A/G]CTGGGAAAAGAAGTT | 10213 |
rs528728500 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408721 | TTGTTCAGTAAATTA[A/T]TTGAATAAAAGTTGT | 10213 |
rs528751707 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400638 | GGTTCACTGTAGCTT[C/G]CACCTCTTGGGCTCA | 10213 |
rs528767295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409898 | ACCCTTGTTATCTTT[C/T]CCACTACTTATTTTA | 10213 |
rs528789213 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401334 | GGAGAGTCAAAGTGA[C/T]ATACAGATTTTCACC | 10213 |
rs528796846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346658 | AACTGTTTGATTCTT[G/T]CTAGTTTTGCTTTTA | 10213 |
rs528817228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338164 | CCTTGATGAAGCATC[C/G]CTAAGGTAGTTTTTT | 10213 |
rs528831661 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307336 | TACAGTGGGGAGAGA[C/T]GAAAAAGAGGCAAGT | 10213 |
rs528845040 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362277 | AGAATAGTAAAGTCA[A/G]CACTTACATCTGTAT | 10213 |
rs528857883 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315487 | ATGAAAACTGAAAAA[A/T]AGACTACAGAGATGA | 10213 |
rs528868817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314977 | TTAACTTTTTGAGGA[A/C]CTGCCAAACTGTTCC | 10213 |
rs528952787 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333187 | TGTATGTCTTTCCTT[A/T]CTGTTCCATATCTTC | 10213 |
rs528987442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363244 | CCCTGCCCCAAAACT[C/T]GAAAAATGGTCTTCC | 10213 |
rs528990417 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161308089 | TAGTTTTTGAGGAGG[A/G]CAATAATAGTAGTGA | 10213 |
rs529009599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355687 | CCTTATCAGAATAAT[A/G]AAACATAATTGGAAA | 10213 |
rs529055256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330714 | CACTGGGCAGCCTCT[C/T]AGTGCTGCTTTTTAA | 10213 |
rs529135209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391295 | AGTGTTTCCAAATAT[C/T]ATTCCATTATTGATG | 10213 |
rs529164297 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381261 | ATACATATATAATAC[A/G]TACATTATATATATA | 10213 |
rs529218774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371377 | TTCTGTTTACAGATA[C/T]ATTAAATAAAAATCA | 10213 |
rs529225997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332647 | GTTTCAAGTATTACA[C/G]TGCTTAATGCTGTGG | 10213 |
rs529265482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333144 | GTTTAATAATAGCAT[A/G]GAAATATAAATTTCT | 10213 |
rs529272733 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317493 | GCGGGGCTTGGGTGG[C/T]GTTTCTGAGGTGCCA | 10213 |
rs529303771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325166 | ATATAATGCCTGTAA[A/G]TTGTCACTTTGTATC | 10213 |
rs529326729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383751 | TATTTACTGTTAACA[C/G]TTAGGGTGGCAATTC | 10213 |
rs529334899 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392172 | TATTACAATCTGAAC[A/C]AGTTTCCCCCCTTTA | 10213 |
rs529344917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384940 | AAGGTATAAAGTCTT[C/T]CATAGTCACAAGAAG | 10213 |
rs529354640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393928 | TCATGATCACTGATA[C/T]AGAATCCAACCCCAA | 10213 |
rs529376287 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346917 | GCATTGATCATTATT[A/T]AGCTGAATACTCAAA | 10213 |
rs529438633 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313789 | ACATACTTGTCTTGT[C/G]TAGATCAGTTCTGTA | 10213 |
rs529457948 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389750 | CAAGAATTTCCTGAC[A/G]TGTATTGTGGCATAG | 10213 |
rs529464569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347264 | AATGTAGATTTAGTT[G/T]CTGTTACTCTATCTG | 10213 |
rs529498794 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161411111 | GTGTAATCTATTATT[A/T]TATTAGCTACTTAAC | 10213 |
rs529585102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401984 | AAGGATTGTGATATA[A/T]GTGAAGTATCTGGCA | 10213 |
rs529619012 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335089 | AATTAACAGAATTCA[A/G]GGAGTTTTTATGAGA | 10213 |
rs529624958 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392980 | AGCCATTTTCCTTGG[A/C]ATAAAAAGCAAATAT | 10213 |
rs529652783 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336048 | TTATAAGCCTAGAGG[C/T]GTATGTTTAATGCTG | 10213 |
rs529667330 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331201 | TCCCATTTGTGATTT[C/T]TGGTTATTGTATTCA | 10213 |
rs529670732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161328345 | CAATATGCATAATAG[A/C]CCTTACAAACATAGT | 10213 |
rs529718395 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371967 | TTCATTCATTCTTTC[-/T]TTTTTTTTTTTTATT | 10213 |
rs529718455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378168 | AAATTTTCTTCAGTC[A/G]TAATTGATCCCTCAG | 10213 |
rs529740461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397903 | AAATAAATCGCTCAC[C/T]GTATTTTAAATAGTT | 10213 |
rs529755371 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378839 | ACTTGTTTGTTGAGA[C/G]GATTAGCAAGATAAT | 10213 |
rs529801449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320007 | ATAACACCTGTATAA[C/T]TCATTCTCTCAAGAG | 10213 |
rs529845862 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329808 | GAAAATTAAGAAAGG[G/T]GTCAGGTCAAAAGCA | 10213 |
rs529861161 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161367604 | TTGCTTTCACTGTAT[C/T]TTTTACTTTGGAATA | 10213 |
rs529901769 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351762 | CGTGGTATCATTACT[C/G]TGGGACTCAAGCTGA | 10213 |
rs529955454 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396993 | CTGCAACACCCAGCT[A/G]ATTTTTATATCTTTT | 10213 |
rs529975515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343326 | CATTCAATATTTGTC[A/G]TTTTGTGACTGGCCT | 10213 |
rs530067138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353391 | AAAAGTCACATCCTC[A/G]GAAAAACAACCATTG | 10213 |
rs530108880 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408621 | TTTTCAATACTTTCT[A/G]TGTATTTCTTGTCTG | 10213 |
rs530118299 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345186 | CAATGGACTATTAAA[C/T]GTTAAAATTTATTTC | 10213 |
rs530120389 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306288 | ATGAATGAATTCTTT[A/G]AAGTCTGCATTGTTT | 10213 |
rs530174327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346095 | GCCATGTTGCCCAGG[C/G]AGTTCTTGAACTCCT | 10213 |
rs530187115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369029 | TAGAGAAACACTCTA[C/T]ATGTTAACCAAAGGT | 10213 |
rs530210739 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161385740 | AATTAGATTTGCTCA[C/T]ATGTGAGTCAGTTTT | 10213 |
rs530222898 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161361130 | ATAGCATTTGTTACA[C/G]TTTAATTTTTTAAAA | 10213 |
rs530258011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337115 | TCAATTTCAGGAATG[C/T]TCTGTATCTGTATGA | 10213 |
rs530292854 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313173 | GTATTTGAATCTGGC[A/T]CTCTGACTGTAGAGT | 10213 |
rs530321091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360458 | CATCCCGTGTTCAAG[C/T]GATTCTCCTGCCTCA | 10213 |
rs530352532 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352569 | TAAGGACTAGGACCA[A/C]ATCTAACTGGTTTGT | 10213 |
rs530376824 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324588 | CTTGGTGATTTTTAC[-/T]TTTTTCCCCTAGGTG | 10213 |
rs530404183 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358625 | AACCCTTGACTCATA[C/T]GTTTTTCTCCTTAAG | 10213 |
rs530405728 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329903 | CTCTGTGAAAAATAG[A/G]GTGTTCCTGAGAGGC | 10213 |
rs530409054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320987 | TGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 10213 |
rs530441880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330448 | CAACATTGTTTTACA[C/G]ATTTGATTTACTGGT | 10213 |
rs530454465 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313878 | CCTGTGTGTGTGTGT[A/G]TGTGAAAATATGCAT | 10213 |
rs530455677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361188 | GTGGTGGTATAACAT[A/G]ATATAGGAAAGGAAA | 10213 |
rs530471183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379076 | TACTGCCATGCTAAC[A/G]AAGTTGAGCCCATCT | 10213 |
rs530502956 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344043 | AGTAATCTAGAGATT[A/T]TTTAAAGTGTATGGA | 10213 |
rs530533267 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408489 | AGAGCAACAGAACAG[-/A]AATTAGTACCACAGT | 10213 |
rs530560375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390126 | TAAAGCAGATACTAG[C/G]TGCTCATTAAATGTT | 10213 |
rs530565832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313196 | TGTAGAGTCATAGTA[C/T]TTGACTCTCATGTAC | 10213 |
rs530607715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406148 | ATATAAGAAACTTGA[C/T]CATTAGCAGAAAAAA | 10213 |
rs530615193 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379816 | TAGTGCTCAGAAAAT[A/T]TCAGCCAGGCTGCTG | 10213 |
rs530624863 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335220 | TTCCCTGTTGTCTCT[C/G]TTCCCTTCTTTAGAG | 10213 |
rs530626468 | in-del | -/TT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315859 | TTTTTTTTTTTTTTT[-/TT]GAGACCGAGTTTCAC | 10213 |
rs530654873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369917 | TTAACTCGATCGCCA[A/G]CAGCAGTTTGGTAGT | 10213 |
rs530676090 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322183 | AAGACCAGATTATTA[C/G/T]GCAACAAAGACTTGT | 10213 |
rs530683971 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345805 | ATATTTTTTCTGCTT[-/A]ATAATTGTAGATGGC | 10213 |
rs530699269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352436 | TTGCTTTTATTATAT[C/T]ACCAAGACTTACTCT | 10213 |
rs530735944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344015 | TAGCATTTACATTGT[A/G]TTAGGTATTATAAGT | 10213 |
rs530753424 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397018 | TCTTTTAGTAGAGAC[A/G/T]GGGTTTCACCATGTT | 10213 |
rs530757641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336314 | TTAAGCAGAGTCACC[A/C]TATTAATAAAACACT | 10213 |
rs530758770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407227 | ATATGTTTTGTCAAT[A/G]TTTCCATTTATGTAA | 10213 |
rs530790039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161398348 | GGATGCCAGTTAGGT[C/T]CTAAAGTAAAAGAAG | 10213 |
rs530873389 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345686 | TGAACTTCATGTGTC[C/T]GAAGGCCTGTTATTT | 10213 |
rs530874069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401141 | TTGATAAATAAGTAC[A/G]GTACTGTAAATGTAT | 10213 |
rs530879323 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391379 | CACCTTATTGGTAGG[A/T]GCTGAAGTGGGAGAG | 10213 |
rs530881748 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378787 | ATTCTCTACACTGCA[C/G]TTTCCTCATCCATAA | 10213 |
rs530905989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346174 | AGGCGTGAGCCACCG[C/T]GCTCGGCCATTTAAT | 10213 |
rs530926409 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408665 | GATGCTGATAGTTTT[A/T]ATTGCCCTGAAGGTT | 10213 |
rs530928867 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407120 | GTATGGAGTACAAAC[G/T]TATGTGAATTGTTCC | 10213 |
rs530943059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338048 | TAAAAAATGATGAGA[A/G]AATCTAAAAACATTT | 10213 |
rs530966953 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390224 | TTAGAGAAGTGGTGG[A/T]TATTTTGGTTAGTTT | 10213 |
rs530969002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361236 | CCAGTACTAAGAAAA[A/G]ATGAAAAATTAAAAT | 10213 |
rs531069167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331349 | CTCAGTGCAACCTCC[G/T]CCTCCCAGGTTCAAG | 10213 |
rs531108646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362028 | GTTTGGTTTTTCTTC[C/T]CCAGTGACTTAGTAA | 10213 |
rs531141268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345425 | TTTTTCTATTTTTTG[A/T]ACAGACAGGGTTTCA | 10213 |
rs531160755 | in-del | -/T | 0.482159 | 0.0927485 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357903 | AATGACTTCCTGTTC[-/T]TTTTTTTTTTTTAAT | 10213 |
rs531165079 | snp | A/G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358900 | AGCCATCTAGCACAT[A/G/T]AAGTATCTTGAAAAC | 10213 |
rs531214559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341444 | AGAAGTTCTTTATCA[A/C]ATATATAATTCGCAG | 10213 |
rs531231602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403896 | AACTTTGTTCTTCTA[A/T]CAAATGAATTTAAAT | 10213 |
rs531269762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404737 | GTTATTTTCCTTGTC[C/T]TCTTGCCTTCACATC | 10213 |
rs531269826 | snp | A/G | 2.97473e-05 | 0.00385652 | missense | PSMD14 | GRCh38.p7 | 2:161395100 | TAAATTTGCATAAGA[A/G]GAGTTGGATGGAAGG | 10213 |
rs531292898 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403980 | ATACTATCATAGCTC[A/G/T]CTGCAGTCTTGAACT | 10213 |
rs531299560 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400886 | CAAGGTATGTCACAA[A/G]CGCATAAAATATAGG | 10213 |
rs531356777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364994 | CTTGTAATCCCAGCA[C/T]CTCAGGAGGCTGAGA | 10213 |
rs531416070 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317010 | AATGTATACTGTATG[C/T]TGTTTGTTTTTTCTG | 10213 |
rs531447153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386549 | TTTTAAAGGATTGAG[A/G]TGTGTTGATTTGAAA | 10213 |
rs531476038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333828 | ACCAGGTCAGGAGTT[C/T]GAGACCAGCCTGGTC | 10213 |
rs531489580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365538 | TTTCTAAAAAAAAAT[A/G]TTTTCAGGCAAGTTG | 10213 |
rs531526822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358195 | CATAATAATTTCTCA[A/G]TAAATAAAACATGAT | 10213 |
rs531616922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311778 | TGCCATCACGCCCGG[C/G]TAGTTTTTATATTTT | 10213 |
rs531676464 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161353408 | AAAAACAACCATTGA[A/T]ATTTAAACAGTATTC | 10213 |
rs531697217 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358977 | TTTTGTTGTTTATTC[A/C]GTTCTTTTTCTGGAG | 10213 |
rs531725477 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321517 | TGACACAAACCTGGC[A/G]GTTACTGTCAGACTC | 10213 |
rs531737099 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320869 | TAGCTGGGATTACAG[A/G]CGTTCACCACCACGC | 10213 |
rs531767414 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392509 | TAATCTATATGCTGG[C/G/T]GGGGAGGATGTGCAA | 10213 |
rs531807790 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349382 | GCATCAGAATGCCTG[C/G]TTGGCATGTTTGTGG | 10213 |
rs531832777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359512 | AGATTTTTTTTTTAA[C/T]TGGACTTGGAAAAAG | 10213 |
rs531844663 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161356155 | TAAGTCGACATGAAA[G/T]AATTCATTTCCACTT | 10213 |
rs531861400 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387741 | GTAGAATTATGAGAT[A/C/T]TTTTTGTCTTTCCTT | 10213 |
rs531899109 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376788 | TGAGACTTCTTTGAG[C/G]AGAGATACCAATTCA | 10213 |
rs531903019 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333205 | GTTCCATATCTTCAT[A/T]GCTCATCCTTATATT | 10213 |
rs531921135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326695 | AATAAAATGCATATA[C/T]ACTCATTCCTTAGTA | 10213 |
rs531958571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327382 | AGTGGCAAATTTTAT[A/G]TATTTACTACAAAAA | 10213 |
rs532020002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334415 | GCTAAGGTTTGTGTG[G/T]TGTTCTCTCTCCACA | 10213 |
rs532045508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161377492 | TATACTATTTATGAT[A/G]GAATAACATGTAATA | 10213 |
rs532048838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387973 | TATATGATAATGTAT[A/T]TTATTTTTATTTTGC | 10213 |
rs532084605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376855 | TAAATGTTTATAAAA[C/T]AAAATCGAGGAATGA | 10213 |
rs532084980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388687 | TTTTCAGTTTATCAA[A/T]ATAAAATAAATTAAG | 10213 |
rs532137891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358302 | ATCACTTAGTCCATT[G/T]TAGTTGAATGTAAAT | 10213 |
rs532201644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396952 | CCTGCCTCATCCTCC[A/C]AAGTAGCTGGGATTA | 10213 |
rs532212078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310573 | GATTAAATAATCTCT[C/T]CTAGTTCTAAAATGA | 10213 |
rs532214006 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377352 | GGTATTCTTGGAACA[A/G]GTTTTGTTACTGTAT | 10213 |
rs532280996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335034 | CTTCTGTCCCTTAAC[C/T]TCTACCATGCCTCAG | 10213 |
rs532469212 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341826 | CTGGGAGACAGAACA[A/G]GTCTCCTTCTCCAAA | 10213 |
rs532470788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407286 | CCAGTTAGGAAATAC[C/T]TTTATAACTGAAAAT | 10213 |
rs532476390 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161361161 | AAACATGTAACTCTT[C/T]AATCCATCTGGGTGG | 10213 |
rs532497209 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335524 | TTCTAGAGATTGTCT[C/T]ATCCCATATCCATAG | 10213 |
rs532506907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161398522 | CCTAATTTATTCATG[C/T]GGAGATGCATCTGCT | 10213 |
rs532511278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351871 | GGCTGAAGAGGGTCA[C/G]ATGTTCATACCTAAC | 10213 |
rs532544191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312995 | TAGTGTTTATTATAT[A/G]CTTACTATATGATAA | 10213 |
rs532646542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407864 | CATTTATCAGATGCT[A/G]TGAATAAATCATAGA | 10213 |
rs532651089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352483 | CCACTAGAATAATAA[A/G]CTACACCAAGTTACA | 10213 |
rs532676866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368209 | TAGCAGAGTGTTAGT[C/T]TGATTTTGAACCAAG | 10213 |
rs532689012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344118 | GAGACTTGGTGCGGG[A/G]GGGTGGGGAGCGGTG | 10213 |
rs532717869 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383142 | TATTTTGATAGGTTG[C/T]TCTAAAGGATAAATC | 10213 |
rs532774930 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358505 | GCGCTGTCTCCTTTC[C/T]GCTAGGTAGCTCCTC | 10213 |
rs532797567 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316087 | GACCTCAGGTGATCC[A/G]CCCGCGTTGGCCTCC | 10213 |
rs532835685 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161327315 | GTGGTATTGGTTGTG[C/T]GACAGTGTTAATGTG | 10213 |
rs532918244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355840 | TGGATCCGCAAACAG[A/G]AATGTAAATGGAAAC | 10213 |
rs532948488 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161308246 | AGAGAAAAAGGAGGC[A/G]TCGGCGGGGCGCGAG | 10213 |
rs533005397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382875 | ATTTCCCCTACCAAC[C/G]CATACATTAATTAAT | 10213 |
rs533098947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373738 | ACCACTTTCTTGAAC[A/T]TTTTGTATATTTCCA | 10213 |
rs533138112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326086 | TCTGTCACCCAGGCT[A/G]GAGTGCAGTGGCATG | 10213 |
rs533141355 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331876 | TAATCCTCACAATGA[A/T]CCTACATGGGTAGGG | 10213 |
rs533141714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323363 | TTTTTTTAATATCAC[A/G]TTTTAAAATGTTAAT | 10213 |
rs533252262 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375634 | TTTTTTCCACAGATA[G/T]TAGAATGTAAAATGA | 10213 |
rs533286180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365650 | TATGAATACAGTGTT[C/T]GTTAACCTATTTTTC | 10213 |
rs533294643 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318035 | GGTTTTCAAGCTTGT[A/T]AGAGTATCTTCTGTA | 10213 |
rs533302402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315518 | AGTCTCTAGTGTTCT[A/G]TATCTTTTTGAAAGA | 10213 |
rs533310761 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398538 | GAGATGCATCTGCTA[-/T]TTTTTTTTTAATTTT | 10213 |
rs533355391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332794 | TCTGCTGCTCTGGCC[C/T]GTGCTGGGATTACAC | 10213 |
rs533370141 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340528 | AGTGGTAAGAAAAAT[C/T]CCAGTCCAGGGTCTG | 10213 |
rs533390334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402982 | GTGGAAAACAGTTTG[G/T]TGGTTCCTCAAAAAG | 10213 |
rs533409808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374920 | TGGGTTCCTGTTAGT[A/T]AAATGCTCAGTTATT | 10213 |
rs533499273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333212 | ATCTTCATTGCTCAT[C/T]CTTATATTTTATAGG | 10213 |
rs533506026 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330412 | ATCAAAGATACAATC[-/TG]TGTTTTCTTTCCCTA | 10213 |
rs533511425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309814 | TTTGGGAGTTTTTGG[C/T]TTTTTGTTTTTTTTT | 10213 |
rs533536886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348219 | GATACTGGGACATTC[A/G]TAACAGCATTGCTTA | 10213 |
rs533540891 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339919 | TACTGCTTTAAAAAA[A/C]TGTTTTAACCAACAA | 10213 |
rs533571283 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363011 | GTGTCCTCATATGAG[C/T]CTGTGACCATAGAAA | 10213 |
rs533587317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402217 | CAATTTTCCATTCTG[C/T]AGAATGATCTTTCTA | 10213 |
rs533595907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393143 | GCCTTACTCGAGGGT[C/T]GCAAGGGAATCCTTG | 10213 |
rs533623647 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393276 | GTATAGCATAGGTAG[A/C/T]TGTAGCAGCACCCAC | 10213 |
rs533633895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394063 | GCAACCTCCGTCTCC[C/T]GGGGTCCAAGTGATT | 10213 |
rs533676951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385126 | CTGTCATTCATTTTG[A/G]TTAGGTAAAATTTAG | 10213 |
rs533688097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332846 | CATAGCCTTTCCAGT[A/G]ATTTTGGTTGGGGAT | 10213 |
rs533699761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355898 | TTTCTAAACACTATC[C/T]CCTCTATCTTCTTTT | 10213 |
rs533701446 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401048 | GATATGTACTATAGA[C/T]AGAGGTCTGCAGCTG | 10213 |
rs533726434 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161308339 | CGCCGTCTGTCCCAA[C/G]AGCTCCTCCTGGACA | 10213 |
rs533772080 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340065 | TCTAAGAAAAGGCAT[A/G]GGTCAAGAAATCTTT | 10213 |
rs533779891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401569 | TAAGAAGGTGACTGT[C/T]GGATTCTGCCATAGA | 10213 |
rs533783740 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332316 | TTCTTACTTTTTTAC[A/G]TCTTTAAAACGTTTT | 10213 |
rs533789237 | in-del | -/TGA | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376657 | TTTCCTTGGGCATGC[-/TGA]TGAAAAGGAAGTGAA | 10213 |
rs533819724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392387 | CAAACTGTTTCTCAC[C/T]AAGGTGTCTTAGAAG | 10213 |
rs533837596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383309 | AAGACAGTTGCTATA[A/G]TGATGGCAGCAAATT | 10213 |
rs533860288 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326229 | AGAGACAGGGTTTCA[C/T]CATGTTGGCCGGGCT | 10213 |
rs533876012 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384275 | TAGTCTAGGTTTGTA[A/T]TTTTTGTTATTGTCT | 10213 |
rs533896561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357791 | ACTATTTTATGTAGC[C/T]TAAGTACCTCTTTAG | 10213 |
rs533945853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309965 | CCTGGCCAAGACTAG[A/C]CTGGCTAACATAGTG | 10213 |
rs533983237 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161316394 | AAGTTTTCCTCCTTA[A/G]ATTATCAAAATAATT | 10213 |
rs533992660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315615 | TATTGCATTATTTTC[C/T]ATATTCTTGTCATTT | 10213 |
rs534052753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341018 | CTGCTCCTCCGCCTC[C/T]GCTGGCGCCGCCGCG | 10213 |
rs534069645 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346504 | TCCTTACTGTGGGCC[A/C]TATTTTTTTTGCTGC | 10213 |
rs534172739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317300 | TACCACGTTTTCTTA[G/T]ATGCCTTTTCATTTT | 10213 |
rs534174603 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309292 | CTGTGTCTGTCAAAA[G/T]AAAAAGAATGTAAAC | 10213 |
rs534192578 | in-del | -/TTGT | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360364 | GCTGAGCCTTTCATA[-/TTGT]TTTTTTTTTTTTTTC | 10213 |
rs534206803 | in-del | -/ATAAA | 0.00199481 | 0.0315187 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307197 | AATAAATAAATACAT[-/ATAAA]ATAAAATAAAATAAA | 10213 |
rs534247560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403361 | CATAGAGACAGAAAA[C/T]AGATGTGTGGTTGCC | 10213 |
rs534260544 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318957 | GAAAGAAATTATCCC[C/T]AAGAAAATCACCTAA | 10213 |
rs534293284 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358444 | AGACATAAGGGTAGG[A/G]GTAAAGGGACTTGGA | 10213 |
rs534341261 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376865 | TAAAATAAAATCGAG[A/G]AATGAATTTGCATCA | 10213 |
rs534433011 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353559 | AGAATGCCTTTTCCC[C/T]CCCTCCCCCTTTTCT | 10213 |
rs534438984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344565 | TATTGTTTTTCACAG[C/T]GAATGATTATCTTTT | 10213 |
rs534475188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375080 | TGATCAAAACACTCA[A/G]TGGACTTTAAAAAAT | 10213 |
rs534526085 | in-del | -/AAC | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326384 | CTATTATCCAAATTA[-/AAC]AACAACAACAACAAC | 10213 |
rs534526731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357047 | ACACTTTGAGGCATT[A/G]GTTTTTATGCTGTTA | 10213 |
rs534532990 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161329016 | CCTTACCTAGGTATT[C/G]CATTTTCTCTCCCAG | 10213 |
rs534615581 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391643 | GTCTCCCAGACTAGA[A/G]TGCAATGGTGTGATC | 10213 |
rs534694136 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311355 | GAACATGTATAGACA[-/T]TTTTTTTCATTATTC | 10213 |
rs534737600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381729 | TAAGTAATAAACCAG[A/G]TTCGTCATTAAAATG | 10213 |
rs534773166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371703 | ACATTTTAAAAATCT[A/G]TTTAAAGGGCATTGT | 10213 |
rs534779577 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161377423 | TTTGAAGTTTTATAA[C/T]ACTCTCAGATCTTGT | 10213 |
rs534790485 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329110 | AGAAAATTCTCTTCT[C/G]AGTGAGTTGGGAAGC | 10213 |
rs534848530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345504 | GACCTCAAGCAATCC[A/G]CCCACCTCTGCCTCC | 10213 |
rs534895773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379179 | TCCACTAGAAAGGGA[C/T]CTGAAGTCACTGGTT | 10213 |
rs534988581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380503 | AAAAAAAGTAAATTA[G/T]GCAAGTTACACCCCA | 10213 |
rs535006544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314356 | AGAAATATATTGTTC[A/G]CTCATTGACACTTTA | 10213 |
rs535015399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391486 | TTTCTGATTAACTTA[C/T]CTTCTTCAATAAAAA | 10213 |
rs535027355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323462 | AAGGCTAGGAGTTCA[A/G]GACCAGCCTGGCCAA | 10213 |
rs535041619 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331550 | GGCGTGAGCCACCGC[A/G]CCTGGCCTCTTTGGA | 10213 |
rs535044297 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322880 | CCATTCATTCTAGTT[C/T]CTTAATTTTCTCTAA | 10213 |
rs535092822 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306511 | TTGAAATGACAAAAC[C/G/T]GCAATTTTTTGCACC | 10213 |
rs535110500 | in-del | -/AT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161408231 | TACTAAAGATCACTC[-/AT]GTGGAGTAGTTTCAG | 10213 |
rs535137082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362494 | AATATTTATTTGAGG[A/G]GTGGGATGCTCAAGT | 10213 |
rs535172553 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396227 | AACATCACAGGCAAG[A/G]GCTAGGAGATAGAAA | 10213 |
rs535225465 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408224 | TCATGGTTACTAAAG[A/T]TCACTCATGTGGAGT | 10213 |
rs535226565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346293 | GATAAAGTTTTGTCA[G/T]GCCTCTCTGAACTCA | 10213 |
rs535254994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400158 | GGCTTAAACAAGGTA[A/G]AAAGGTATGTCTCAT | 10213 |
rs535257999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406278 | AGAGCTGTGCAGACC[A/G]TGCATGATGGGATAG | 10213 |
rs535296558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390680 | ACTGAATTAGGAAAA[C/G]GGGAATTCCAGATTA | 10213 |
rs535400397 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161350727 | ATTTATAGTTAATCA[C/T]TAGATTGCTGTAATG | 10213 |
rs535407339 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314093 | AATTGCAAAACATTT[A/G]TATTTTTAGATTTAT | 10213 |
rs535459138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324599 | TTACTTTTTTCCCCT[A/G]GGTGTTGTAGTTTCA | 10213 |
rs535466579 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354421 | GGCTAATTTTTGTAG[-/T]TTTTTTGTAGAGACG | 10213 |
rs535495392 | snp | C/T | 2.30779e-05 | 0.00339682 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408832 | CCTTTGTGTTTCATT[C/T]ACAGGCTGTAGAAGA | 10213 |
rs535497895 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331168 | TGTACCTGGTTTCAC[A/G]GTTTCTGGTTATTTC | 10213 |
rs535532222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363558 | ATTTTGTTCATGATT[C/T]CTATATTTAGGTGAC | 10213 |
rs535535465 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393487 | AGTTTTGTATCTTCA[A/G]AAGCCTTATAGGTGA | 10213 |
rs535564782 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310897 | TCTACCCACCTGCCC[C/T]GATAGATTATAAATT | 10213 |
rs535674339 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391513 | AAAAGGCCTTTTGTA[A/G]TTAAATTAGTAATAT | 10213 |
rs535686504 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369363 | TTCTTCTTCTTTTTT[A/T]AGACAGTCCTTTTAA | 10213 |
rs535723292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360857 | TTTATTTCATCATGT[A/G]TTTCTGATGTAATTA | 10213 |
rs535735640 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381843 | CTAAGACAGATGTAC[-/A]AAAAAACATGCAGTT | 10213 |
rs535737819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392186 | CCAGTTTCCCCCCTT[G/T]ACTATTACAATTAGT | 10213 |
rs535756543 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371964 | TTTGTTCATTCATTC[A/T]TTCTTTTTTTTTTTT | 10213 |
rs535763499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361553 | TGTTTTATAACTCTA[A/G]CATAATGATATCAAA | 10213 |
rs535777564 | in-del | -/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324659 | TTTGAAGTATGAAGA[-/T]TTTTTTTTTTCTTTC | 10213 |
rs535864498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315237 | GATGTTAAACATCCT[A/G]TGATGCGCAAGACAG | 10213 |
rs535918405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367325 | TTTGATATTTGCAAA[G/T]GTGTTTTGATTATGT | 10213 |
rs535978030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359169 | TGGAGATGCGGTCTT[A/G]CTATGTTGCCCAGGG | 10213 |
rs536001640 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363170 | GGGATCTAGGTTGCA[C/T]GCTCCATCTATAATG | 10213 |
rs536061299 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333988 | GTGAGCTGAGATGGC[A/G]CCACTGCACTCCAGC | 10213 |
rs536070859 | in-del | -/ATC | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307789 | CCTAGCACAAAGTAG[-/ATC]ATGAGTAAAATGTGA | 10213 |
rs536094079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395294 | AATTAAAAATAGAGA[A/G]TCCTGTTTTGTAAAT | 10213 |
rs536122133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381880 | TTGTATTGGCAGCTT[A/C]CAAATATTTAGTATC | 10213 |
rs536138005 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359779 | TGAACTAAGCTCCCA[A/G]AATAAAAGTAGACTT | 10213 |
rs536144146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376442 | ACTAGAATATTAAAA[A/G]AATAGAATGTGAATG | 10213 |
rs536147317 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405164 | TTGAAACTTTGGACT[C/T]ATCTCTCTTGCTCTT | 10213 |
rs536179152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334531 | TAAGTAAATTATTCA[A/G]TATATTAAGACATTT | 10213 |
rs536186135 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323938 | CTTCGTTGTCTTTAT[A/T]ACAACTCCACCTAGG | 10213 |
rs536192789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326917 | TTTTTATTGTTGTAT[C/T]GTTATTTTTTATTGT | 10213 |
rs536253497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329257 | TTCTATTTTTATTCT[A/G]TATCTGCTAGAGCAA | 10213 |
rs536275871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389234 | AGTTACTAGCTTTAT[A/G]ACCACCATGTAGGGT | 10213 |
rs536276701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318558 | AACTTAATGATAGCA[A/G]AGTTTTGAAAGTATG | 10213 |
rs536401719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351618 | CCCTGGAAGTCTTCT[A/G]TGGTGTGCTAGTCAG | 10213 |
rs536402102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311861 | CTCAGGTGATCCAAC[C/T]GCCTCGGCCTCCCAA | 10213 |
rs536500233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406636 | AGGCATTTGATTTGG[A/G]ATATCTTAGAATTGA | 10213 |
rs536529043 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322546 | AGGCATGAGCCTCCA[C/T]GCCCAGCTAATTTTT | 10213 |
rs536615841 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339215 | TTCTTCAAAAACTGC[C/T]AAATTGTTTTTCAGA | 10213 |
rs536649673 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336420 | TGTAGGTTCTAAAAC[C/T]GGATGAATTATGGAA | 10213 |
rs536678790 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386667 | TACTTGCATGTTCCA[A/G]GAGAATATATTATTG | 10213 |
rs536725067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389650 | AAATATTTTAATACT[C/T]ATTGGAGTGATTTTT | 10213 |
rs536735733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359935 | ATTACCTCACAAGCT[C/T]CTCGAAGCTTTTGTT | 10213 |
rs536750004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379344 | TTATTTGTCACTTGT[A/G]AGTGTAGAAACACCG | 10213 |
rs536771888 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360642 | TTACAGGCATGAGCT[A/G]CTGTGCCCAGCCCTA | 10213 |
rs536793667 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330192 | TGACATTCTGATGAA[A/G]TAAGAAAAAATAAAA | 10213 |
rs536817810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334645 | GAGAAAATGGGAACA[A/G]ATGTGACCATGTTGA | 10213 |
rs536849796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312442 | AGCCACTGCACCTGG[C/T]CAAAAATTGATTTAT | 10213 |
rs536854315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327820 | AAAAAGTTATGAAAA[G/T]ATAGTCAGTGTCACT | 10213 |
rs536930919 | snp | C/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307127 | AGTGAGCCCAGATGG[C/T]GCCACTGCACTCCAG | 10213 |
rs536935947 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322041 | TAGCCCTCTAATTAC[C/T]GTGTTGGTCTTTATG | 10213 |
rs536945719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372891 | ATATAATTAGAATTC[C/T]ATTTTGTAGTATTAG | 10213 |
rs536945871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351931 | TATGTGCCTGAGAGA[A/G]CGGAACCAGAAATAT | 10213 |
rs536959775 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161367535 | GTCTATATCTCTTCC[C/T]TGGCACTGTTAAAAG | 10213 |
rs536975357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343550 | ATCTGTTTGAGGATC[A/G]GGTACAGTGGCTCAC | 10213 |
rs536982097 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342176 | GAACCTTTAATAAAA[C/T]GTTAATAGAAGTGGT | 10213 |
rs536990665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161328947 | ACTTTTTAGAAGAGC[C/T]ACCAAATAAAGTCAG | 10213 |
rs537019790 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337306 | TAGAATTGCTCTTTT[C/T]TGGTATCAGTAAACT | 10213 |
rs537031451 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312540 | AGTGGAAAGTAATCA[A/G]CTTTTGAAAGTACTG | 10213 |
rs537040309 | snp | A/T | 0.089084 | 0.191327 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389912 | TTTTTTTTTTTTTTT[A/T]AGAGATGGGGTATTG | 10213 |
rs537070067 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320086 | AAACATTCTAGAGAG[C/T]TTCTAGAATTTCTCT | 10213 |
rs537083102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379387 | TAGTATCAAGATTCT[A/G]GGCATATTCAGTCAT | 10213 |
rs537098888 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368548 | TTAGACTTGTGTTGA[C/T]AGATGTGCATTTTGA | 10213 |
rs537177050 | in-del | -/TAA | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333132 | ATTTTAAAATTTGTT[-/TAA]TAATAGCATAGAAAT | 10213 |
rs537205178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343723 | ATTTTAGCTCCTCGG[G/T]AGCCTAAGGCTGGAG | 10213 |
rs537206563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352661 | TTTTTTTCAAATAGT[C/T]GTGCCCACATTCACC | 10213 |
rs537229456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406656 | CTTAGAATTGAAGAG[A/G]TATGCTTACTCTTTT | 10213 |
rs537275641 | snp | C/G | | | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161412026 | ACAAAGAAAAGGGAG[C/G]AATTTTAATTTAGAC | 10213 |
rs537354955 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345435 | TTTTGTACAGACAGG[G/T]TTTCACTATGTTGCC | 10213 |
rs537361364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378366 | ACTGAGCAGTGATAA[A/G]TAAAGACTATATTGT | 10213 |
rs537400709 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336178 | ACCTTTTATTCATTT[A/T]ACTTACTTGAATTAT | 10213 |
rs537435426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321590 | CAGATGCCAGCTATA[C/T]TTCATGTGTCCCCAA | 10213 |
rs537437975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393777 | TAATGATGGTCCTCA[A/G]TTGAAGAAAATTTGT | 10213 |
rs537438131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403142 | AGTTGGAGACAATCC[A/G]AATGTCTATCAGTAG | 10213 |
rs537474766 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394238 | TGGCCTCCCAAAGTG[C/G]TGGGATTACAGGCAT | 10213 |
rs537499184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322692 | ATTGCGCCCGGCCTG[C/G]TCATGTTTTTTTAAT | 10213 |
rs537518170 | snp | C/T | 1.86771e-05 | 0.00305585 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385461 | GACACCTTGTTTTTA[C/T]AGGTTGTTATTGATG | 10213 |
rs537524810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380127 | TTTATTACCAAGTCT[A/G]TGAGGCATCGTCATT | 10213 |
rs537577076 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357836 | TCGTTTATTCTAATA[G/T]GTATTATTAAATGAC | 10213 |
rs537585320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326239 | TTTCACCATGTTGGC[C/T]GGGCTGGTCTCGAAC | 10213 |
rs537601617 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394157 | TTGTGTTTTTAGTAG[C/T]GACAGGCTTTCACCA | 10213 |
rs537669731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407422 | AATGATGTGTTGTAA[A/C]TAAGTATCCTTTGAT | 10213 |
rs537674174 | in-del | -/TTC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161369348 | TGTCTCTGTTGCATA[-/TTC]TTCTTCTTTTTTAAG | 10213 |
rs537742405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347698 | GGATTTCTTAAACAA[A/G]ATAGCACAAATAATA | 10213 |
rs537745716 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344379 | GACTGCTGGCTTCTT[C/G]TTGTATCCTCGCATA | 10213 |
rs537805064 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161410267 | AAAAAATATATTGTA[A/G]TCTAGTCACTTAATT | 10213 |
rs537809695 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332893 | GGTGATGCTCATTGC[C/T]TATGGGCCATGGAGC | 10213 |
rs537810033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349922 | ACTTCAAAGTTGATA[C/T]TGATTTCCAACAAGA | 10213 |
rs537851001 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358433 | TTGGAAATATGAGAC[-/AT]AAGGGTAGGGGTAAA | 10213 |
rs537869191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404288 | GTCTCATTTTATCTT[C/T]AGTACACTGCCAGAT | 10213 |
rs537882760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384553 | TATAGAAATACTGTT[A/T]CTTAGTATATGATCT | 10213 |
rs537948567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341997 | AATTTTTAAATGTCG[C/T]ATTTTTGTTTGTGAT | 10213 |
rs537982161 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322395 | GTCATGTTATTGTTA[C/T]TATTATTATTTTGAG | 10213 |
rs538033475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310029 | AGCCGGGCATGGTGG[C/T]ACGTGCCTGTATTCC | 10213 |
rs538034729 | snp | A/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307367 | GTTCATACTCTTAAG[A/T]TTCTGATTAGGAAAA | 10213 |
rs538049096 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161308932 | CCGGTCTGCTTTGAA[C/G]TTTTTCAAAGCAGAC | 10213 |
rs538068297 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314315 | TTGAATAAGTAACTG[A/G]GTAAGAATGTCACTT | 10213 |
rs538082270 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312633 | TGTTAGGTATAAACA[C/G]TTTATTCATATTGTC | 10213 |
rs538170463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340112 | TGCTTCTGCTATAGC[A/G]GAGTGGAGATTTGGC | 10213 |
rs538277866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386751 | TGCTTCATTATTTTT[C/T]GCAAAAGGTTAAGTA | 10213 |
rs538289055 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405274 | TGCATTCTTTATACT[C/G]TCATCCTGACTCTCC | 10213 |
rs538295546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395656 | TTATTGAAAATCTAA[G/T]GTGCCAGGCATATCA | 10213 |
rs538316604 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376104 | ATCTATGTATATATA[C/T]ACATATATATATATA | 10213 |
rs538408582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348700 | GTATAAAGAAATGCA[C/T]GATCACTAAGATGAG | 10213 |
rs538417293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318243 | ATATGTTTAATGTTT[A/T]TGCTATAGTATTTCT | 10213 |
rs538481850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375951 | TATCTAGAAGGTCGT[A/G]TCTTTTCTTTCAGGG | 10213 |
rs538488775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403194 | GGTATGTACTTACAA[C/T]ATACTATTACTCAGT | 10213 |
rs538524356 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161328028 | GCTTAGATCTTTACC[C/T]GGCAAATAACAGACA | 10213 |
rs538524790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357900 | AATCAATGACTTCCT[A/G]TTCTTTTTTTTTTTT | 10213 |
rs538524857 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365910 | CTGTTTAACTGAAAC[A/C]TTATTATTATCCTAA | 10213 |
rs538551715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385793 | TATCATATTTGAGGA[C/T]CCCCTTTTTGGGAGC | 10213 |
rs538556465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340764 | TTATCTCTCAAGCTT[C/T]TAAGATGCCAAAAGG | 10213 |
rs538561160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358607 | TACATTTCCCCTCAC[C/T]GAAACCCTTGACTCA | 10213 |
rs538584593 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306358 | GTGGTCAACTAATGA[A/T]TAGAGAGACAGGTTT | 10213 |
rs538591371 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331348 | GCTCAGTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 10213 |
rs538628648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317704 | AAGGTGATTGGTGGG[A/G]GATAATATATAAGTA | 10213 |
rs538661267 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405343 | ACATTTACTTAACCC[C/T]TATGTCCCCATCGTG | 10213 |
rs538670285 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375275 | TTATTCTGCCAATTA[C/T]ATACTGATAACCTAC | 10213 |
rs538691344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318423 | TTAATTTAAAAGTGA[C/G]GATTTTTATTTGTAC | 10213 |
rs538775618 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161409268 | CTTTATCAATATGTA[C/G]GTAATATTCCTGAGA | 10213 |
rs538787772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340128 | GAGTGGAGATTTGGC[C/T]GAGCTGGTAAGAACC | 10213 |
rs538850143 | in-del | -/TT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338343 | TAGGGTTAGGAGAGT[-/TT]TTTTTTTTTTTTTTG | 10213 |
rs538875664 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311065 | TAATCCCAGCACTTT[G/T]GGAGGCTGAGGCTCA | 10213 |
rs538983079 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161364078 | AAGTAGCTCTTAGCA[A/G]ATGGGGGAGCCAGAA | 10213 |
rs538994631 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342826 | AATGATTCCATTATA[A/T]CCCCTTTGTTGAATT | 10213 |
rs539040506 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363425 | CTTTTACCCTTGTTT[A/C]TCCTAGTGTGATTTT | 10213 |
rs539045988 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313800 | TTGTGTAGATCAGTT[C/G]TGTATTTCAAATACA | 10213 |
rs539076022 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347438 | CATGAGCCCACTGCA[C/T]CTTATTTACTTTTTA | 10213 |
rs539093550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397345 | AAATAAATAAAGCAT[G/T]GCACTGGTCGGATAG | 10213 |
rs539118534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401475 | TGCAGTGTGTGCAAT[A/G]TGGTCTTTTAGCTGG | 10213 |
rs539126264 | snp | A/C | 5.62709e-05 | 0.00530399 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318920 | TGTGTAAACTACAAG[A/C]CTTTTTGTAGTTAGC | 10213 |
rs539135387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343462 | TTGTCCATTCATCTA[C/T]TGATGAGCAGTTGGG | 10213 |
rs539139929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389130 | CCTTCAGACACCAGT[C/T]AATATTTCATTAGTA | 10213 |
rs539155116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346836 | TGTGGGAGGTAGGTG[C/T]ACTCTTCCCTGTAAT | 10213 |
rs539191080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339155 | TCTCTTGCTTAAATA[C/T]CTAGGATTAGATTGG | 10213 |
rs539239183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315033 | AGAAAATTAATCTAG[A/G]GTATTATCATCTCAA | 10213 |
rs539286301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358636 | CATACGTTTTTCTCC[G/T]TAAGTTTTTTCATGT | 10213 |
rs539302236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359043 | ACACAATCACAGCTC[A/G]CTACAGCCCCAGCCT | 10213 |
rs539324970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350004 | TTCATAAGAGGGAAC[C/T]GGGAATGTCCATTTG | 10213 |
rs539364819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351303 | TACTAGGGCAGAAAG[A/G]AGGTTGCAGAGTAGT | 10213 |
rs539392107 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398826 | AGTAGCTATATTAAA[C/T]GGAGAAATCTCATTT | 10213 |
rs539396628 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307454 | CATAGGTTTGGGGGG[G/T]AAGCATAAAGATGTG | 10213 |
rs539431494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309161 | GTTAACTTACTTTCA[A/G]TATCATACTAATTGA | 10213 |
rs539436514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400939 | TTGCTACCATAAAAC[A/C]TACACTAATCTACTA | 10213 |
rs539492999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364516 | CCAGCCCTGCCTTGG[C/T]CCCCCTCCCCTCATA | 10213 |
rs539529423 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356921 | TAATCAGCAGGTATT[G/T]TAATAACATAATAAA | 10213 |
rs539565155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357753 | GTGTGCTTATTTTAT[A/G]GTGGCATTGTATGAA | 10213 |
rs539598746 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306667 | GCACACCCTAAGCAC[C/G]TTCTACAGTCTCAGG | 10213 |
rs539615613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332220 | GAATATTTCATTTTA[C/T]TCCCTATGATAATGT | 10213 |
rs539637095 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314188 | ACATTTGTGTACACT[G/T]TAGCATTTTTCCATG | 10213 |
rs539653308 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324627 | TCATGAAGATTTTCT[G/T]TCTTTCTTTTTTTTT | 10213 |
rs539667434 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380758 | TTTCATTGGAAATGG[A/C]ATAAAAAGTAAGATT | 10213 |
rs539742541 | snp | A/G | | | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161412153 | AGAAAGTATATGTCT[A/G]AAAAGCAAAATGAGA | 10213 |
rs539807154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323194 | GAATTTTTTAAACTG[C/T]CAAGTCTATTGGCCT | 10213 |
rs539845105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391819 | GCTCAGGTTGGGCTT[C/G]AACTCCTGTGCTCAA | 10213 |
rs539848970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324207 | TATTATATACTATAA[C/T]GAATTCCAAGACGAA | 10213 |
rs539860971 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378119 | ATGTCTTCTTGTCAT[C/T]GTAATTTTCTAAAGA | 10213 |
rs539882004 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161411880 | TATAATGATTTCCAT[C/T]AATGAGTGGCTACCT | 10213 |
rs539981115 | snp | G/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307449 | AGAGGCATAGGTTTG[G/T]GGGGGAAGCATAAAG | 10213 |
rs540023398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408582 | CAAATGGTCAACACA[A/G]TCATTTAGTGATCCT | 10213 |
rs540094802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373181 | ATGATGAATTTCATT[C/T]AAAAATATGTATGTG | 10213 |
rs540108260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383970 | ACTTGTTTTTATTGC[A/T]TTTTTAAAAAAGAGA | 10213 |
rs540134607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363647 | TGTAGATGGTCCACA[A/G]CCCCACATTTTTCTC | 10213 |
rs540186271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347912 | TGAAGCATAAAAAGC[A/G]AACAGTGAGCTACGG | 10213 |
rs540189834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339673 | AGTCAACGACCTATT[A/G]TATCAATTAGATCCC | 10213 |
rs540197985 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392050 | TTTAACATTACCTGA[C/T]GTTTTGATGAATTAG | 10213 |
rs540222124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381182 | AAAATTATTTCAGTT[C/T]GTCACTTATGTTTAC | 10213 |
rs540258834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382475 | ATAATAAACAAAAAA[C/G]GAAAGTAAGAGGTTT | 10213 |
rs540296906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372378 | ATCTGCTCACCAGCA[C/G]AAAAACTAAACATGG | 10213 |
rs540318603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340297 | CCAAGCCAGCCAGAG[A/G]GAGAAGTGGGGTTCC | 10213 |
rs540324094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363122 | CATTATATTCTCATA[A/G]GAGCACAAACAGTAT | 10213 |
rs540332050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373489 | AGTCCTCTCATCTCT[A/G]TGAATCAGATTAAAT | 10213 |
rs540373460 | in-del | -/TT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161319779 | GTTTTTGTTTCAGAC[-/TT]CATGAAATTTTCAGT | 10213 |
rs540381702 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346034 | CTACAGTCATGTGCC[A/T]CCACTCTCAGCTAAT | 10213 |
rs540412455 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315022 | TCTTAAGTTTGAGAA[A/G]ATTAATCTAGGGTAT | 10213 |
rs540445995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400504 | AGAATCTTTTTTGAG[A/G]TGTACAACAATTTGA | 10213 |
rs540491382 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360174 | TTTCCACCCCGTAAC[-/AT]ATATATATATGCATG | 10213 |
rs540521499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337725 | TATATTTTTCAAAGT[A/G]TATAAACAGGTACAT | 10213 |
rs540597374 | snp | A/G | 7.9466e-05 | 0.00630291 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161371283 | GTCGGAGAGAGCTGT[A/G]GCAGTGGTTGTGGAT | 10213 |
rs540654746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405899 | GAAGTATGATGTGGA[A/C]TAAGAGAGATACAGG | 10213 |
rs540655144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402758 | AGAAGACAATCCAGT[A/T]CAAAATTAGGCAAGG | 10213 |
rs540680712 | in-del | -/ACTC | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372655 | ACTATATGTGTTGTT[-/ACTC]AACATATAGATAAAA | 10213 |
rs540693568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396973 | GCTGGGATTACAGGC[G/T]CCCGCTGCAACACCC | 10213 |
rs540708325 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365563 | AAGTTGAGAAAGGCT[A/G]TGTCAAGATACCAGT | 10213 |
rs540729824 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161409496 | TGGAACATGGTTATC[A/G]TATTGCTGATGTTGG | 10213 |
rs540743963 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351447 | GCCATATTATACTCT[A/G]TAAGTCCTCAAGTTT | 10213 |
rs540756217 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335060 | CTCAGAACTTCTGAG[A/C]CTTTTATGCTTCTAA | 10213 |
rs540859957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355532 | TTTGACATTTCCATT[C/T]TTATTTTCTTTCTTT | 10213 |
rs540893142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311382 | ATTCCCTAAGCAATA[C/T]AGTATAACTATTTGT | 10213 |
rs541027869 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161328650 | AATTTAAAGAGTCAC[A/G]TGTACCTGTTGAGTC | 10213 |
rs541080548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397779 | GCTTTGAAAAGTATG[A/C]CCTGATTATAGTGTT | 10213 |
rs541103976 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382765 | TTGGTTAAGTTACTG[-/T]TTTGAGTTTATAAGA | 10213 |
rs541119627 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306799 | TTTTTTTTTTTTGAC[C/T]TTTATAATGAATGTT | 10213 |
rs541146100 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335889 | TTATAAAATAGGCAC[A/T]GTAGAATCCACTTTG | 10213 |
rs541148209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361822 | CAGTCTTTTTGTTTT[A/G]ATTGTTACTCGTAAG | 10213 |
rs541164155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330285 | TGACATCTGATACCA[C/T]TTTTGGTAGAAAGTA | 10213 |
rs541175572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407918 | TCTTGTCTTCAGGCC[A/G]TAACATACCCAAACT | 10213 |
rs541209494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312154 | AAAGTAATTTTTTTT[A/T]TTTTTTTGAGATGGA | 10213 |
rs541240183 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358507 | GCTGTCTCCTTTCCG[C/T]TAGGTAGCTCCTCCC | 10213 |
rs541253422 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378667 | TCAGGACAGCTATTA[A/T]AACAAACAGCTTTAT | 10213 |
rs541260917 | snp | A/G | 2.0264e-05 | 0.00318302 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367746 | ACCAGAGACCTCAAC[A/G]AAATTTGCTTTGTGT | 10213 |
rs541298015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359402 | GGTTTTTATTTTTCT[A/G]TCATTTGTGTGCTGT | 10213 |
rs541325959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368896 | GCTACAGAATGCAAT[A/G]TATTTAAAATAATGT | 10213 |
rs541360401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330334 | AGAAGATATCTCTGT[C/G]TAATATGGGAAATTA | 10213 |
rs541380034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336213 | ATATATATAGCCATC[A/T]ATAAATTACTTTTCA | 10213 |
rs541396214 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161353156 | GAAAAGATACTCTAT[A/G]TCATAATAGTGAAAT | 10213 |
rs541403486 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402972 | TACAGCCACTGTGGA[A/C]AACAGTTTGGTGGTT | 10213 |
rs541512514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353370 | AAAGATGACCTTGCT[C/T]ATTTGAAAAGTCACA | 10213 |
rs541517073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336838 | CCTCAGCCATCCAAA[A/G]TGCTGGGATTATAGG | 10213 |
rs541530417 | in-del | -/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307447 | GAGAGGCATAGGTTT[-/G]GGGGGGGAAGCATAA | 10213 |
rs541533771 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380435 | CATTAAAGCATATAC[A/G]TTCAAAACTTGTGGA | 10213 |
rs541568145 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384704 | TGTGATTCTTGTTAA[A/T]CTCTTTATATGTAAG | 10213 |
rs541645581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312849 | TGCGAAATGCAAGTC[C/T]CTATCTCCAGTGTGA | 10213 |
rs541738661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343923 | GCATCCATGGATTCA[A/G]CCAACGTTTACATCT | 10213 |
rs541747875 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161399648 | CTCACTGAAGACAAA[C/T]GGTGTATAAACATGG | 10213 |
rs541795014 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398420 | TCAAGTCTGAATTCC[A/C]CACAAATTCTGCTTG | 10213 |
rs541801555 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321987 | ACTCAAAATTCAAAT[C/T]TCCATCCTCCCTTCC | 10213 |
rs541861702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390083 | TGCCCTACCTTACAG[C/T]ACTATGAAGATTAGA | 10213 |
rs541862145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399375 | GGAAGAAAATATTTT[C/T]ACCTATAACACAGAG | 10213 |
rs541869407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362763 | TTTGGTTTCTCTACT[C/T]GTATGGTTTTAGACA | 10213 |
rs541889233 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389943 | TATGTTGTCCAGGCT[-/G]GGTCTTGAACTCTTG | 10213 |
rs541939240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330381 | TCTCAATATTCCAAA[C/T]GTATGGGACGTTATG | 10213 |
rs542011692 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388173 | TACTAAATATTGATG[C/G]ATAGATGCATGTGCT | 10213 |
rs542046741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390859 | GACTGAGCAAGGCTA[C/T]TGAAACTGCTTAATT | 10213 |
rs542053056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322951 | TTGTTCTTGGATCTC[A/G]TTCTCTTGACACACT | 10213 |
rs542053350 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369842 | TTCAATTATTTCGTA[G/T]TTCTGGTAAACATAT | 10213 |
rs542079092 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344807 | CACAAGCCTGCTCAT[A/G]TGATTTTCAGATATT | 10213 |
rs542086506 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352384 | GCTTACATTCATTGC[A/T]TATTTACTTTCTGGG | 10213 |
rs542092301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370807 | TGTCCATTGTTAAAA[A/G]TGTACTCTGTGCCTG | 10213 |
rs542093952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380663 | TTATAAATAATTTCC[A/G]TGTTGCAAACTTGAG | 10213 |
rs542150219 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161379634 | TTAACTGTATCAGTT[G/T]GGGTCTTCTGTGGAT | 10213 |
rs542221251 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393573 | GTAAACTTCTAAGCA[A/T]GTAGGATAATTTTTC | 10213 |
rs542252795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366328 | ATTCTAGAACCTTTT[A/G]TACTTAATGCTTCCA | 10213 |
rs542257179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354282 | AGACAGAGTCTCACT[C/T]TTGCCCAGGCTAGAG | 10213 |
rs542262572 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306950 | AAGAGCATTCTAAAA[A/C]AGTAGCCTGGGGAAC | 10213 |
rs542296806 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358041 | GACTTTTTTTCCATT[A/T]CTTTTTTTTATAGTG | 10213 |
rs542323942 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405355 | CCCCTATGTCCCCAT[C/T]GTGCTTTGTGCACAC | 10213 |
rs542337575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349229 | CAAATCCTAATAGTT[A/C]CCCTTTCTCTAGCCT | 10213 |
rs542436288 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313918 | TTTACTATTCTAACT[G/T]TCTGGTGTACAGTTT | 10213 |
rs542438884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374755 | CAAATTTAGAAGTTA[A/G]TTCAACTTGTAATGT | 10213 |
rs542445882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384791 | AAGAATATACTTATT[A/G]TAATATCTTTACCAT | 10213 |
rs542475699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375572 | ACCTCATGGGAAGAA[G/T]GTAGAAACAATATCA | 10213 |
rs542477653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364973 | GCCTGGCGTGGTGAC[A/G]TGCCCCTTGTAATCC | 10213 |
rs542481925 | in-del | -/TAAATAACAT | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161328891 | GTCATGGAATAACAC[-/TAAATAACAT]TAAATAACATTAAAT | 10213 |
rs542516215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365498 | AATGCATTTTGGTGA[C/T]GGTTTGATGTTTTAT | 10213 |
rs542601893 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360368 | AGCCTTTCATATTGT[-/T]TTTTTTTTTTTTTCA | 10213 |
rs542645559 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356107 | TTTTAAATTAATTGA[A/C]AGCAAACAGCTGAAA | 10213 |
rs542667568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310370 | AACTGTGCTTTTTTA[A/G]TTTTCAATTTTGTAG | 10213 |
rs542670283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312279 | CTCCTGAGTAGCTGG[A/G]ATTATAAGCACCCGT | 10213 |
rs542687611 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320764 | GGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAATG | 10213 |
rs542714336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320382 | TTATATGTCAATGGC[A/G]ACTTCAAAGCTTTAT | 10213 |
rs542717409 | snp | A/C | | | missense | PSMD14 | GRCh38.p7 | 2:161395126 | GAAGGTTTGACACTT[A/C]AGGACTACAGTGAAC | 10213 |
rs542723972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350135 | TGGCTTAAGCTAGGC[A/T]GAACAAATAAAATGT | 10213 |
rs542744535 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336421 | GTAGGTTCTAAAACC[A/G]GATGAATTATGGAAG | 10213 |
rs542759823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341396 | CCCCGTCCTTTGTTA[A/C]TGAATTTTATGAGTT | 10213 |
rs542772835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333633 | TTTAGGATCTTGTTC[C/T]TATTCTTCTTCCAGA | 10213 |
rs542778463 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406569 | AGACAAACTGGTCTT[G/T]CCCAGATGGTAGATG | 10213 |
rs542891059 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161411187 | TTAAATTGTAAAATA[A/T]TTAAGTAAGGTCTGG | 10213 |
rs542904596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317875 | ATTTCATTTAGGACA[C/T]AGCGATTTTCAAGTA | 10213 |
rs542968687 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337496 | TTTAAGTGGTTAAGA[C/T]AGGATTAAACCTCAG | 10213 |
rs542981696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327188 | AATGATAGAAAGCAG[A/G]ATGGTAGTTGCCAGG | 10213 |
rs542989837 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354085 | TTGCAGTCTTTTGTG[G/T]AACAATTCTGATACC | 10213 |
rs543004001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319679 | CCTTTTAAAATCTCT[G/T]TAGTTTCCAGCTTTC | 10213 |
rs543007857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388514 | TAAAGTACAAAGTCA[C/T]TTAGCAAAAACTCTC | 10213 |
rs543043724 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376720 | TGATTAATGTATTGC[A/T]CTTAACCATTTTGTA | 10213 |
rs543109409 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161377111 | TTAATAGTCATTTGT[C/T]TACTAAAAGTAGGAA | 10213 |
rs543138355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342402 | TGTATCGAGATGATT[A/G]TATGACTCCTTTGTT | 10213 |
rs543145475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368674 | TGTATTTTTCCAAGC[A/G]ATATTTCTTCTTTGC | 10213 |
rs543171155 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332416 | TTGGGAAAAAGGCTT[C/T]TCTTGTTAAGCTAAT | 10213 |
rs543234103 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335832 | TACTACTTAGTCACT[G/T]TTTAGACATTGATTA | 10213 |
rs543249517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375586 | ATGTAGAAACAATAT[C/G]ATTCCAAGTGGTACT | 10213 |
rs543266841 | in-del | -/TAC | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403758 | GCCTGAAGCACTCCT[-/TAC]TACTACTATATTCCC | 10213 |
rs543282359 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318015 | TTTCTTAACTTCTTC[G/T]GTGAGGTTTTCAAGC | 10213 |
rs543283029 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366649 | TTCCCAGATTGTCCA[A/G]TATTAAAAAACAAGA | 10213 |
rs543319622 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358753 | TTTGAGACCAGTCTG[G/T]CCAACATGGTGAAAC | 10213 |
rs543485968 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351647 | AGGAAAGGTTGATTA[C/T]GTTTCAGGAATAACC | 10213 |
rs543521093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369737 | ATATTTGTAGAACTT[G/T]GGATGAGGCTCATTT | 10213 |
rs543524528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343118 | TCATTTTTAAGTGAT[C/G]AGTTCAGGTATGTTC | 10213 |
rs543591444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396914 | CTCACTGCAACATCT[A/G]TCTCCTGTGTTCAAG | 10213 |
rs543600215 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387335 | GGAATTTTATTTTAT[G/T]TTAGCAGGATCTTTA | 10213 |
rs543616866 | snp | A/C/T | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326184 | CACAGGTGCCCACCA[A/C/T]CACGCCCGGCTAATT | 10213 |
rs543625944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397601 | GTTATTACACCAAAA[C/T]GTAGTATTTCCCTTT | 10213 |
rs543636319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376532 | GAATATGGTAATGAC[C/T]ACAAAAGAAATGAAG | 10213 |
rs543656981 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311223 | CTGAGGAAGGAGAAT[C/T]GTTTGAACCTTGGAG | 10213 |
rs543666512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389272 | GTAGTGAGTGCATCG[C/T]GCAAATGTGCTTGGA | 10213 |
rs543713379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161377894 | TGTGCCAAGAGTACA[C/T]TGGAATTATAGAGAA | 10213 |
rs543744132 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161381771 | CCTTGACCCTTGGGC[A/T]TGCTTGGAATAAATA | 10213 |
rs543765692 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406568 | AAGACAAACTGGTCT[C/T]GCCCAGATGGTAGAT | 10213 |
rs543794315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378609 | CACAAACCTTGCTGT[C/T]GAGTATAACTGAACC | 10213 |
rs543806366 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405839 | TATAGTGCGAACAAA[A/G]TTAACATGTTAATGT | 10213 |
rs543902907 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373661 | CAATGATTAGATCAA[G/T]AATTAAAATGACATT | 10213 |
rs543942361 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360944 | TGTGTACTGACTTCT[G/T]GTCATAAATGGGAAA | 10213 |
rs543982786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401038 | TGAATTGCTTGATAT[A/G]TACTATAGATAGAGG | 10213 |
rs543989448 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161327215 | CAGGAGCTGGGAAGA[G/T]GAGAGAATAGGGAGT | 10213 |
rs543991677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334883 | GATGTGTGTTTTTCT[A/G]TCTGTTCCCTTAATT | 10213 |
rs544016780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401642 | TATATACACACACAA[A/G]CATGTGTGCACATAC | 10213 |
rs544055336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392468 | GCTTACCCCCTCTTT[C/T]AACCAGATCACATCC | 10213 |
rs544124903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335741 | AAATTCCTAGGAGTG[A/G]AATTACTGTGTTTAA | 10213 |
rs544134957 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357919 | TTTTTTTTTTTTAAT[C/G]GTGGTGAAACAGTTG | 10213 |
rs544158432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333182 | ATTGTTGTATGTCTT[C/T]CCTTACTGTTCCATA | 10213 |
rs544186467 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349037 | CTTTCTATCTTAGGC[C/T]GAAGACAGATCAGCT | 10213 |
rs544293332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333646 | TCCTATTCTTCTTCC[A/C]GAGTAGATCACAATT | 10213 |
rs544298667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364113 | GATGGTTTTCCACTG[A/G]AGTCAGGACGCTGTC | 10213 |
rs544314519 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388417 | AGTACTCATAACCAG[A/G]CTGCTTCATTCTTTT | 10213 |
rs544335691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364823 | AAAACAGCACTCATG[A/G]CTGGGTGCAGTCGCT | 10213 |
rs544335765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356414 | TAGTTAGTTGTATGT[A/G]TTTGAATTCATTTAT | 10213 |
rs544377209 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348493 | GCCCAACTATCCATC[A/G]GTAGGAGAATGTGTA | 10213 |
rs544490865 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391931 | ATACCATGTTTACTC[-/T]AAAGAAAACTAAGCT | 10213 |
rs544513699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331818 | GGACTGATGCTGAGT[A/G]CCTTCCTTATTCTGA | 10213 |
rs544548421 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332457 | AATCTTGTTGTACCT[G/T]GACTTGTAATAATGA | 10213 |
rs544554106 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341059 | GCCCTTCGGGCTCCC[C/G]CGGTCCCGCAGGCTC | 10213 |
rs544634506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394551 | TTCATTAATTCATTC[A/G]TTCATCAGATATTTA | 10213 |
rs544668199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309453 | GAAAGTGATTTTGTT[C/T]CACTGGTCACAAGTG | 10213 |
rs544721152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364875 | TTGGGAGACTAAGGC[A/G]GGTGGATTGCTTGAG | 10213 |
rs544746403 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161364874 | TTTGGGAGACTAAGG[C/T]GGGTGGATTGCTTGA | 10213 |
rs544836728 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332588 | GATGTTTCCAGACTA[A/G]GGCATCATAAATGGC | 10213 |
rs544870312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384689 | AAGCTTTAGCAAGTA[C/T]GTGATTCTTGTTAAT | 10213 |
rs544910077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349002 | CCTGGTTCATTGGCC[C/T]CTCACTCCCAGAGAG | 10213 |
rs544963782 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326525 | TAAACATAGGATTAC[C/T]GTATAATCCAGCAAT | 10213 |
rs545016096 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365513 | TGGTTTGATGTTTTA[G/T]TTCCCTTTTTTTCTA | 10213 |
rs545018675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326526 | AAACATAGGATTACC[A/G]TATAATCCAGCAATT | 10213 |
rs545027646 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360597 | TGACCTCAGGTGATC[C/T]GCTTGCCTCTGCCTC | 10213 |
rs545045740 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343300 | TTCAAAGGACCTCAC[A/G]TATATGGAATCATTC | 10213 |
rs545050024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316846 | AGAAACAAATTTGAC[A/C]TGCCAGATTTTCTTT | 10213 |
rs545063308 | snp | C/G/T | 0.00180218 | 0.0299644 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318813 | TTTTTCTTTGTTTCT[C/G/T]TTTTCTAGAAATATG | 10213 |
rs545068106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365356 | TCATTCATTCTTTCA[A/G]TCAGTACTTATTAAG | 10213 |
rs545140813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348242 | ATTGCTTATAACAGG[A/G]TTTGATAATCTTTTC | 10213 |
rs545159493 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348591 | CTAATGAAAAAGCAC[A/G]TGGAGGAATAATTCT | 10213 |
rs545199860 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404071 | CACTATGCCTGGCTA[-/T]TTTTTTTTTTTCTTT | 10213 |
rs545219319 | snp | C/T | | | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161411805 | ACAAAGATATGTTTC[C/T]GTTTGCATTTTAAGA | 10213 |
rs545243711 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395911 | ACACCTTCATATTCA[A/G]ATTGTCCACACACCA | 10213 |
rs545256496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373743 | TTTCTTGAACATTTT[G/T]TATATTTCCATTTTT | 10213 |
rs545285077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332957 | CATTAATGTAAACTC[A/G]TTTTCAAATATCTCA | 10213 |
rs545288216 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316088 | ACCTCAGGTGATCCG[A/C]CCGCGTTGGCCTCCC | 10213 |
rs545292715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403589 | GTGCTTTTAAAAAGC[C/T]TTTGATGACTGACTT | 10213 |
rs545321064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324995 | CTTTTAGCCAGGTCC[A/G]TTATTGAGAATGACA | 10213 |
rs545345037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161308657 | GCAGCCGTGCTAGGC[C/G]GCCGCCAGCCCCGTG | 10213 |
rs545347034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334142 | GTTCGAGACCAGCTT[A/G]ACCAACATGGAGAAA | 10213 |
rs545353365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330586 | CAGATTCATTTAAAA[C/T]CCAAGCAGGTAGGAC | 10213 |
rs545357864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325631 | TTTCAATAAAAATAT[C/T]AACCAGAATGTTCAT | 10213 |
rs545362720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341133 | CCCGCGGGCGAGGCC[A/G]CCGGCTCGGGGGCGC | 10213 |
rs545401891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333710 | GTGGACAAGCTCCCA[A/G]TGAGAGAAAGGTATC | 10213 |
rs545447935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387515 | CACTAATGATTTTCT[A/G]ACAGATTTTTTTTTA | 10213 |
rs545476316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400420 | CTCCTGATTACAACC[A/G]GCCCTGGAACTATAT | 10213 |
rs545521802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161377239 | CACACCTCTTTTCTT[C/T]GTCTAGTTTTCCAGG | 10213 |
rs545618163 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161399041 | AAACAGTTGAAAAAT[A/G]TAATAGGCAAATCAG | 10213 |
rs545664638 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349125 | GTGCAAAATTCACTG[A/C]AAATTTTGCTATTGA | 10213 |
rs545706307 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342178 | ACCTTTAATAAAATG[C/T]TAATAGAAGTGGTGA | 10213 |
rs545809814 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390204 | ACATTGTAAAAGTCT[A/G]TTAGTTAGAGAAGTG | 10213 |
rs545838481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356250 | CAATTAACACCTCCT[A/G]TAACAGGTTGCCTTA | 10213 |
rs545846063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391232 | TTTTTCAAACCATTT[A/G]AACTATTACCTGGTA | 10213 |
rs545935708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401731 | TCTGTGAAATTTTTA[G/T]GAAGCAACTATGTTG | 10213 |
rs545953040 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377663 | TTAATAATATAATCT[C/G]TGATCTAATTTGTTA | 10213 |
rs545959309 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324095 | GTCAATATAAGCTTG[A/G]AAGTAGATGGAACTT | 10213 |
rs545999974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407807 | ATGCTGTGTTGGCAT[A/T]TCTTAAGGTTAGTGA | 10213 |
rs546065512 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344962 | TAAGAAATGCTTGTC[G/T]AACCCAAGTTCATGA | 10213 |
rs546068540 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353048 | TAATTTTATTAAAAG[A/C]ATATTTTGTTCTGAG | 10213 |
rs546150645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362921 | GCTTTGCCTTTGTTT[A/G]TTGTTTCTGTTTATT | 10213 |
rs546200225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401219 | TACTTCGTTGTAACA[A/G]TATAGTATATGATGT | 10213 |
rs546344163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362154 | CACTGCAGCCTCAGC[C/T]TTTCGGGTTCAAGCC | 10213 |
rs546347487 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393181 | ATGATAGGAATATCC[A/T]GTTGCTCCTTGGGAA | 10213 |
rs546370554 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332308 | GTTTACATTTCTTAC[C/T]TTTTTACGTCTTTAA | 10213 |
rs546371196 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307149 | GCACTCCAGCCTGCG[A/T]GACAAAGCAAGACCC | 10213 |
rs546373423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371058 | GGTGCTTTTTCACAC[A/C]TGTGTGTTTTTCATC | 10213 |
rs546379147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354480 | TGATGTTTTTTTATA[A/T]CAAAGGTAGTCGAGC | 10213 |
rs546413403 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382231 | TATTAAAGCTACTAA[C/T]AAGAAGACAGCAGGA | 10213 |
rs546461944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322474 | AGCTCACTGCAGTCT[C/T]GCCCTCCTGGATTCA | 10213 |
rs546464773 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399781 | AGTGGGAAAGTAATT[G/T]ATACATTTTTGGAGG | 10213 |
rs546537254 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410144 | TTTGGCCTACTGCAT[A/G]GCAAAAGCAAAACTG | 10213 |
rs546597415 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393149 | CTCGAGGGTCGCAAG[G/T]GAATCCTTGTCCAGG | 10213 |
rs546602194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361438 | TAATGAACACTTCCA[A/G]AATTGAAAAACACGG | 10213 |
rs546607441 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370055 | ATATACATAGGGAAG[A/C]TTTTTTTCCAAATTT | 10213 |
rs546613102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382885 | CCAACCCATACATTA[A/G]TTAATTCTTGGGAGT | 10213 |
rs546626325 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357342 | GCTTAGATTTTCATG[A/C]ATGAATAAAGGCTGG | 10213 |
rs546630560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331992 | AGCCTATTTATATCA[A/G]CATTTCTTTAGGTAG | 10213 |
rs546650107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372927 | CTTAGGTTTTATGAT[A/G]TCTTGACTCATGTGA | 10213 |
rs546658655 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396306 | GAAATGAAATCAGTA[C/T]GTTGAAGAGATGTAT | 10213 |
rs546728925 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330098 | ATGCAATTATGATAA[A/G]TAAATTTGTTCAAGT | 10213 |
rs546769616 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324570 | AAGGTGTTGAATGCC[A/G]TACTTGGTGATTTTT | 10213 |
rs546831414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346225 | TAACCCCATCTAGTG[C/T]ATTTTTTATTTTGCA | 10213 |
rs546866590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380008 | GGTTGTGAGTCAGTC[A/G]TGCGCTCCACAGCAG | 10213 |
rs546870033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346667 | ATTCTTTCTAGTTTT[A/G]CTTTTAACCCTTGCT | 10213 |
rs546946742 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346508 | TACTGTGGGCCATAT[A/T]TTTTTTGCTGCTTTG | 10213 |
rs546988993 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310613 | CAATTATAACAAGAA[G/T]AGCAACGACAACATT | 10213 |
rs547035049 | snp | C/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306447 | GTTGGGACAAGCCTT[C/T]AACAATCAGCCAAGC | 10213 |
rs547049395 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161330833 | ATAAAAATAATAAAA[A/G]TTATGATAGTTGTAC | 10213 |
rs547053133 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313462 | TCAAGTGGTCCTCCT[A/G]CCTCAGCCTCCCCAG | 10213 |
rs547099237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325155 | TGCAGCAGGGTATAT[A/G]ATGCCTGTAAGTTGT | 10213 |
rs547099864 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366316 | TAGAGAAAACTTATT[A/C]TAGAACCTTTTATAC | 10213 |
rs547169420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404831 | ACTTTTTGGCAACTA[C/T]ACACTCTGCTGCCTT | 10213 |
rs547218059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410083 | AATTGGCAAAGTTTA[A/G]TAATCATCAGAATCA | 10213 |
rs547235055 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363000 | CTGTAATTCAGGTGT[A/C]CTCATATGAGTCTGT | 10213 |
rs547265589 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341855 | AAAAAAAAAAAAAAA[A/T]TAAAATTAAAAAAAA | 10213 |
rs547286380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403970 | GGGCTGCATGATACT[A/G]TCATAGCTCACTGCA | 10213 |
rs547288206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331483 | CAGGCTGGTCTCGAA[C/T]TCCTGACCTGGTGAT | 10213 |
rs547310166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391503 | TTCTTCAATAAAAAG[C/G]CCTTTTGTAATTAAA | 10213 |
rs547322802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334459 | GTAGTTAATAGATAA[C/T]CTTGATTAATCAATA | 10213 |
rs547355233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396386 | TCAACCTAAGTGTCA[A/G]TCAACAGACAGATAA | 10213 |
rs547389244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407314 | AATAATAGAGTGACA[C/T]CTGACTCTGAAAATG | 10213 |
rs547390608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333923 | GTAATCACAGCTACT[C/T]GGTAGGCTGAGGCAG | 10213 |
rs547423734 | snp | C/T | 0.000179024 | 0.00945939 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161395197 | ATTAGCCAAGAATTA[C/T]AATAAGGTAAAAGTT | 10213 |
rs547458856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327534 | TCCCCAATCCCCCCA[A/T]TTTTTGGGGCAGAAA | 10213 |
rs547477218 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161327770 | ACAAAAAGATGACCT[A/C]ATTTAACAAAAGAAT | 10213 |
rs547488084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319229 | GAAAAAGTAAGCATG[C/T]CATCCTGCTTGCCAG | 10213 |
rs547575687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378064 | CCATTGTTATTTGTG[A/G]GGATATTTCTGGACC | 10213 |
rs547665849 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367195 | GTAACAAATGTGGCT[A/T]ATTGGTACATTATAG | 10213 |
rs547690792 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358920 | ATCTTGAAAACCCTT[C/T]GTATTTGAGACTTCT | 10213 |
rs547718603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404980 | CCTCTCATTTGAAAT[A/G]TATTATCATCTCCAC | 10213 |
rs547775431 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360370 | CCTTTCATATTGTTT[G/T]TTTTTTTTTTTCACC | 10213 |
rs547842487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368499 | TTATTCTTTCTAGAG[A/G]TGTTTGTTTTGTTTT | 10213 |
rs547854488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352543 | TATTTTCTGTCTCCT[A/G]TATTACATTTTAAGG | 10213 |
rs547886591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336383 | CAAGGAAATGAAGAT[A/G]CTGATACTATTTACG | 10213 |
rs547892891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344168 | CTGCCCCAAGGGTAC[C/T]GAGGGATGACTATAC | 10213 |
rs547898616 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335881 | TTCCCCATTTATAAA[A/G]TAGGCACAGTAGAAT | 10213 |
rs547943345 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321574 | AGAACTACCCTTACT[G/T]CAGATGCCAGCTATA | 10213 |
rs547972828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329879 | TGATTATTCTGAATA[C/T]GTATTAAACTCTGTG | 10213 |
rs547994910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368366 | TTTTAAGCTTTTCTT[A/G]TTTAAAATGTTAAGT | 10213 |
rs548010241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312431 | TTACAGGCATGAGCC[A/C]CTGCACCTGGCCAAA | 10213 |
rs548026246 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342630 | TTTGCTTTTTTTTTT[A/T]AAAATCCAGTCATAG | 10213 |
rs548044542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311812 | TAGAGACCAGGTTTC[A/G]CCATGTTGGCCAGGC | 10213 |
rs548062484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334595 | CTGTCTTTTTAAAGT[C/G]CTCCTCTGTAGAGCA | 10213 |
rs548079635 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354158 | GGCCCCTCTTTCCAG[G/T]TATGTTTTTGCCAAT | 10213 |
rs548114951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351904 | CAAGAGGTTAGGGAA[G/T]TGCAGTCGTACTATG | 10213 |
rs548123824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161328374 | GTAAGAGAAAAATTC[A/T]GTTGTAAAAAGATAC | 10213 |
rs548130998 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351815 | GACTCCTTAAAAAGC[G/T]TTGATTGAAAGTGAC | 10213 |
rs548146714 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161398656 | AATTTGCCTTTTTTT[C/T]CCCAAGCATGTAGTG | 10213 |
rs548154143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388915 | CAAAAAGGACATGGC[C/T]GGTTGACTTATGATT | 10213 |
rs548182182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400003 | ATCTCTATCTTGCAT[A/G]TATGTCAACATATTG | 10213 |
rs548191819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378252 | TCACTTTCCATATAG[C/T]TTTACCATATGCAGT | 10213 |
rs548197444 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338257 | AGAAATGAAGTTCTG[A/C]AACTGCGTTTGTGTG | 10213 |
rs548234389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388214 | GCCTCTAAGTATAGT[C/G]TTGAGTACAGTTGCA | 10213 |
rs548272952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320013 | CCTGTATAACTCATT[A/C]TCTCAAGAGGCCTAA | 10213 |
rs548277698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312512 | CTAATCAGACATAAA[C/G]TGAGAAAGAAAAAGT | 10213 |
rs548315926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400598 | TCACTGTGTCACTCA[A/G]TCTGGAGTACAATAG | 10213 |
rs548371027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405056 | TGTTCAAGAGTAAGC[A/C]ATATTGTCTACCCTA | 10213 |
rs548374339 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359836 | TGTACTGGAAAGTAT[A/G]TTACTAGCGTCAGAA | 10213 |
rs548398211 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161309432 | CATAAAATAGAGTTA[C/T]AGTGTGAAAGTGATT | 10213 |
rs548409663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406069 | TGTTAGTGAAGTGCC[A/G]AAGATCCCATCAGTG | 10213 |
rs548447610 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361209 | GGAAAGGAAATTTAG[C/T]TTTAAATGCTTCCAG | 10213 |
rs548457280 | in-del | -/TT | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383970 | ACTTGTTTTTATTGC[-/TT]TTTTAAAAAAGAGAA | 10213 |
rs548534160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402274 | AAAACTATTTAAAAA[A/C]AGAGAAAAGACAACC | 10213 |
rs548564462 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365575 | GCTGTGTCAAGATAC[C/T]AGTTTAACTTCTTTC | 10213 |
rs548571537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403037 | CCAGCAATTCTGCTC[A/C]TAAGTATATACCCAA | 10213 |
rs548591677 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376430 | AAAGGATCAAGAACT[A/G]GAATATTAAAAAAAT | 10213 |
rs548644485 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378526 | TCATTTCAATAGATA[A/T]TTATTTTGCACTGTA | 10213 |
rs548683120 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337200 | GTACCTAAAAGTCTC[G/T]TTTGGGAGTGAAACT | 10213 |
rs548705271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390418 | TGTCAGAGTTAGATA[C/T]GGGGGCAGTTGTGAA | 10213 |
rs548721027 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337805 | GATCAGGAGATAAGG[C/G]TTCTGGTTCTCAGTG | 10213 |
rs548734007 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322226 | CTTCATTATTTGTAG[A/G]AACAATTCAGTATTT | 10213 |
rs548749642 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388067 | AGTAACTAAATTTTT[A/T]AAACTATTCCATTAT | 10213 |
rs548832095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313180 | AATCTGGCACTCTGA[C/T]TGTAGAGTCATAGTA | 10213 |
rs548845146 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394139 | ACCACACCCAGCTAA[G/T]TTTTGTGTTTTTAGT | 10213 |
rs548891350 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411526 | GGCATCATTTGCAGC[A/G]CTGTAACACCTTCAG | 10213 |
rs548978167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356649 | CTTTTTTGTTATAAA[A/G]CATATATTTTAACAG | 10213 |
rs548999595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310903 | CACCTGCCCCGATAG[A/T]TTATAAATTCTCTCA | 10213 |
rs549004004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348541 | GTGGAAGTTTGTAAA[C/G]TATTGAAAAATGAAT | 10213 |
rs549029710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358771 | AACATGGTGAAACCC[C/T]GTCTCCACCAAAGAT | 10213 |
rs549041687 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340090 | ATCTTTTTAAAGCAA[A/T]CATTATTGCTTCTGC | 10213 |
rs549072861 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349101 | GCCGAATTGGCTTAC[C/T]ATAGGTTGGTGCAAA | 10213 |
rs549107088 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396420 | AAATGTGGTGTATAG[A/G]TATACATACAATGGA | 10213 |
rs549117574 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333361 | ATCCAAATTCCTGAA[A/G]TTTGGCCAGACTTCT | 10213 |
rs549142926 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318954 | AGAGAAAGAAATTAT[C/G]CCCAAGAAAATCACC | 10213 |
rs549146704 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389807 | AATCAGAATGACCTA[C/G]GTTCAGATCCCCATC | 10213 |
rs549195016 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161308840 | GGCCGAATTCACATC[A/T]TGGGAACCTCTTCCA | 10213 |
rs549232167 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161308344 | TCTGTCCCAAGAGCT[A/C]CTCCTGGACATCCGC | 10213 |
rs549248595 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331920 | TATTATAGGGTCGAG[G/T]CACAGAACTAACAAG | 10213 |
rs549262176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357536 | ATTTAGTATTGAGGA[G/T]TTATATAGCAAAAGT | 10213 |
rs549273351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317376 | GAAACAAGCCAGATA[C/T]GAAAAATATATGATT | 10213 |
rs549301597 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347525 | TAGATCATATTAAGA[C/T]AGTGCTGAGATTTTA | 10213 |
rs549310255 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310476 | CTTGTCATATTCCCT[C/G]TTTGTTGCAGTCATT | 10213 |
rs549327724 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317772 | GTAAAACAACATGGA[C/T]GAAGGATGAAATGAA | 10213 |
rs549421885 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386658 | ACAAGCCTGTACTTG[C/T]ATGTTCCAAGAGAAT | 10213 |
rs549433435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366965 | GTTGTATAGGGGGAG[A/G]GGAACAGCTTCATTA | 10213 |
rs549444419 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323598 | AACCCAGGAGGTGGA[A/G]GTTGCAGTGAGCCAA | 10213 |
rs549464586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350911 | CTCCAAGTATTATAC[G/T]GTGGAGTGTGCTTCA | 10213 |
rs549508015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396256 | AAAGGCATAGAACAG[A/G]TCCCGCAATCCCACC | 10213 |
rs549554103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333782 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 10213 |
rs549597792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357640 | ATAAATCATATTCCA[A/G]TTTTCAAATGGTAAT | 10213 |
rs549634433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358290 | TGTCCTCATGTGATC[A/G]CTTAGTCCATTTTAG | 10213 |
rs549658109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375879 | TCTAATTTTTAAAAA[A/C]ATTAAAATAAAAAGT | 10213 |
rs549717664 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375556 | GAAAAGAAGAGCTTG[C/T]ACCTCATGGGAAGAA | 10213 |
rs549732415 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403910 | ATCAAATGAATTTAA[A/T]TTTTTTTTTTTTTAA | 10213 |
rs549797424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341592 | CGCCTGTAATCCCAT[C/T]ATGTTGGGAGGCCGA | 10213 |
rs549815405 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161407719 | GTATCCAAATCTAAC[C/G]CTCACTGGGATTTTG | 10213 |
rs549819575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340702 | AGATTTATGGAGGCA[A/G]CATGCACCCTGGGCG | 10213 |
rs549850502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403150 | ACAATCCAAATGTCT[A/G]TCAGTAGATGAGTGG | 10213 |
rs549924872 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326730 | CGGGGGATTGATTCT[C/T]GGACCTCTGATGATA | 10213 |
rs549936062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312370 | GCTGGTCTTGAACCC[C/G]TGACCTCAAGTGATC | 10213 |
rs549943846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387830 | TTTTTAAAGTACTAC[C/T]TGACAGTGTTGAAAT | 10213 |
rs549976642 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312759 | CTTTTTATTGCTTTT[A/G]TTTCTAAGAATTGAA | 10213 |
rs550060565 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333216 | TCATTGCTCATCCTT[A/T]TATTTTATAGGAAGT | 10213 |
rs550062078 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349436 | AAGCTAAAACTGCAT[G/T]TATTTATAAAGAGAT | 10213 |
rs550155903 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161308219 | CGGCGGCCGCAGAGC[A/G]CAGAGGTAGGGAGAG | 10213 |
rs550234395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351173 | CAAGGGGATGGGAAA[A/G]AGAAGTCCACCTATA | 10213 |
rs550258466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343383 | TGTTGTAGTATGTGT[C/T]AGAATTGTATTCCTT | 10213 |
rs550353202 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390312 | AAAATATCCCTAAAG[A/G]TTTATTTCTGACTTT | 10213 |
rs550369729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376821 | TCTTGGAATTCAGTG[C/T]GTTGCAATAGTTTTT | 10213 |
rs550406986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367071 | GTTGTGATGAATTTG[C/T]AGAGGAATCCCATAG | 10213 |
rs550416797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311786 | CGCCCGGCTAGTTTT[C/T]ATATTTTTAGTAGAG | 10213 |
rs550453546 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319052 | TGTGGAAAACATTTA[C/T]TGTCTTAGTTTACTT | 10213 |
rs550481700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391330 | GCAGCACAAAATAAG[A/G]GAATATTTTATTGGA | 10213 |
rs550546230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372509 | ATGATCCTATTAGGT[A/G]TGATTTAGCTTTTCA | 10213 |
rs550582903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354813 | CCTATGTTACTTTGA[C/T]AGGGTCTCTTTATAA | 10213 |
rs550590700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362315 | TACTATAAAAGATAG[A/G]GCATATTGTATACTT | 10213 |
rs550620315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364480 | GGTGGTGCCTTAGCC[A/G]GGGGCCACACCCTCC | 10213 |
rs550632185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363245 | CCTGCCCCAAAACTC[A/G]AAAAATGGTCTTCCA | 10213 |
rs550655314 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325989 | TATTCTATACAAAAA[A/T]AAATTTGTACCAAAT | 10213 |
rs550718021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374158 | TAATCAGAGTAACTG[A/C]AGAATGCAAAATGAA | 10213 |
rs550752039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331325 | TAGAGTGCGGTGGTG[C/T]GATCTCGGCTCAGTG | 10213 |
rs550794551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322685 | GTGAACCATTGCGCC[C/T]GGCCTGGTCATGTTT | 10213 |
rs550806560 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339052 | AACTTGTTCATGGAT[A/C]ATTTGGTGTGTTTTG | 10213 |
rs550884043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332703 | ATGTTTTTTTAGAAC[A/C]TACTGATCCCATTTA | 10213 |
rs550959973 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339060 | CATGGATAATTTGGT[A/G]TGTTTTGGTTTTTGG | 10213 |
rs551021499 | in-del | -/T | 0.0103295 | 0.0711199 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307247 | TCTGAGTTAAGGCCA[-/T]AAGTGGGGAGTATTT | 10213 |
rs551021804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317035 | TTTCTGTTGGTTCTT[C/T]AAGTTTGTAAGGTTG | 10213 |
rs551034250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355980 | GAGTTGCAGTATTAC[A/G]TTGCAATTAATTTGC | 10213 |
rs551060481 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161308984 | GTAGAATTAACTTTC[A/C]CATTGAATACGTTTG | 10213 |
rs551153718 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382878 | TCCCCTACCAACCCA[A/T]ACATTAATTAATTCT | 10213 |
rs551201938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401985 | AGGATTGTGATATAT[G/T]TGAAGTATCTGGCAC | 10213 |
rs551202018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392248 | CTGGGAAAGTTAAAA[A/G]CATTTTTTAAAAGAA | 10213 |
rs551237679 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339752 | TGTTGAAGGCAATGA[C/G]TGTGTGGCTGTTGCC | 10213 |
rs551329513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410307 | ATGTTGTATCTCTGG[A/G]TTGTTTAAAAAAAAA | 10213 |
rs551331996 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403023 | AGTTCCCATATGAGC[C/T]AGCAATTCTGCTCAT | 10213 |
rs551338787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393040 | ATGTTTATGTTCTTA[A/G]TAGCTCAGTTTAGCT | 10213 |
rs551355458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363368 | ATTTTGGGACATCTA[A/G]AAATTTATATTGTAT | 10213 |
rs551438732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356477 | GAAACTGAATGTAGT[A/G]GTTTCATCAGAATTT | 10213 |
rs551444407 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346324 | CCCCCTGCTTTATCC[C/T]ATTGCTAGTGGTACA | 10213 |
rs551456520 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359039 | AGTGACACAATCACA[G/T]CTCACTACAGCCCCA | 10213 |
rs551462795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318038 | TTTCAAGCTTGTAAG[A/C]GTATCTTCTGTAGTT | 10213 |
rs551477527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347412 | GTCTCCTGAGTACCT[A/G]GGACTACAGGCATGA | 10213 |
rs551482652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309934 | GCTGAGGTGGGCAGA[A/T]CATGAGATGATCCAG | 10213 |
rs551510893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365113 | TCCGTCTAAAAAAAA[A/C]CAAAAATAAAACAGC | 10213 |
rs551524730 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349423 | GAGTCAAAAATAAAA[C/G]CTAAAACTGCATTTA | 10213 |
rs551546024 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371554 | TTTTCCTGAATATTT[A/T]TCTTTAAATTTTTTG | 10213 |
rs551647321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325341 | ATGAATTGAATAGGA[C/T]GTATTTTGTTATAAC | 10213 |
rs551656780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364161 | AGACTCTGCTTCATT[A/C]TGCTGGTTGATAGCC | 10213 |
rs551714133 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161353567 | TTTTCCCTCCCTCCC[C/G]CTTTTCTTACTTGGA | 10213 |
rs551789877 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374961 | TAACTCCTAACAATC[A/T]TTGTGTCTGTTCTCT | 10213 |
rs551815621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310676 | AATTGCTTTGGACGT[A/G]TTTTTACAACAGACT | 10213 |
rs551819650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365659 | AGTGTTCGTTAACCT[A/G]TTTTTCTACTTTTAT | 10213 |
rs551823048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360749 | CACCGTGTTAGCCAG[G/T]ATGGTCTCCATCTCC | 10213 |
rs551859028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358339 | TAGCAATAAAATAGT[C/T]ATAACTTAAGTCTAA | 10213 |
rs551860076 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361250 | AAATGAAAAATTAAA[A/G]TAGAATATGTTCAAT | 10213 |
rs551917626 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379869 | GCCTTTAGAGGAATC[C/T]CTTATTTGGCAGGAA | 10213 |
rs551936643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403000 | GTTCCTCAAAAAGTT[A/C]AACAGACAGTTCCCA | 10213 |
rs551950413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313958 | AAGTATATTCACAGT[A/G]TTATGTAACTGTCAC | 10213 |
rs552017600 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384086 | GTATAAAAAGAAAAA[A/T]GTTTTCACAAACTAT | 10213 |
rs552039523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329028 | ATTCCATTTTCTCTC[C/T]CAGTCTTTAATTTGA | 10213 |
rs552056333 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385128 | GTCATTCATTTTGAT[A/T]AGGTAAAATTTAGGT | 10213 |
rs552076287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329911 | AAAATAGGGTGTTCC[C/T]GAGAGGCCTCAAATC | 10213 |
rs552136539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344018 | CATTTACATTGTATT[A/G]GGTATTATAAGTAAT | 10213 |
rs552187792 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373276 | TATCACTGTCTACTT[C/T]TGTATGTTAGGAAGA | 10213 |
rs552271551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400628 | GCATGATCATGGTTC[A/G]CTGTAGCTTCCACCT | 10213 |
rs552302232 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391613 | TTGTTTTAAGAGATA[A/G]TAGGGTCTTGCTCTG | 10213 |
rs552394630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353527 | TCTGCCTTTCAGTGT[A/G]TCATTTTTATCTTCC | 10213 |
rs552397650 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335373 | GCCACATAGTGCTAC[C/G/T]GAGTCCTTGAAATGT | 10213 |
rs552418099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388995 | AGACTACTTGAGGAT[A/G]TCATTTGATTTAAAC | 10213 |
rs552425171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354442 | TGTAGAGACGGTTTC[A/G]TCATGTTGCCCAGGC | 10213 |
rs552455352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389455 | TTTTTGATCTGTACA[A/G]TATAGCATTTTTATG | 10213 |
rs552483957 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361286 | GGTGATAACTTTGAA[A/G]TCTAAATGAAATGAA | 10213 |
rs552495868 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408121 | TGGAAAGTGGTTTTC[A/G]TGTATTGTTTGGGTT | 10213 |
rs552523186 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306380 | GACAGGTTTTCTTAA[A/T]CACCTTCAACCAAAA | 10213 |
rs552590144 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368326 | TGTCATTTAAAAAAT[A/G]TTCTATATATGGTGA | 10213 |
rs552641969 | snp | C/T | | | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411553 | TCAGTCTCAGTTGTG[C/T]AATTACTTCTGTTTC | 10213 |
rs552655104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345607 | ATTTTTTTCTTTATC[A/G]CTGATTTTGGGTTAT | 10213 |
rs552729631 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323428 | CAGCCCTTTGGGAGA[A/C]CGAGGGGGCAGATGA | 10213 |
rs552729663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331916 | TTCATATTATAGGGT[C/T]GAGTCACAGAACTAA | 10213 |
rs552856881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312800 | TTTATGTTAAGTATA[A/G]CACATTCACTTTGTG | 10213 |
rs552881535 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400078 | GTAACGCCTGAATTA[C/T]TTTCAGTTTTTGCAT | 10213 |
rs552913061 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378454 | AGGAAAAATAAACAT[A/G]AGTGGTAAAAATTTC | 10213 |
rs552918176 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347745 | ATTTTCATCTAAAAA[A/C]ACTAAAAAATAAACA | 10213 |
rs552935338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381732 | GTAATAAACCAGATT[C/T]GTCATTAAAATGAAA | 10213 |
rs552979472 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315395 | TGATTTTGTAGTAAT[A/G]TGAAACATTTTCTTT | 10213 |
rs553058838 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388005 | CTTGGAACATTTGGC[A/T]ATTACTTTCAAATGT | 10213 |
rs553059379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399268 | AGTAAGAATATTAAC[A/G]TGAGCTTTGAAAAAT | 10213 |
rs553065356 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351645 | TCAGGAAAGGTTGAT[A/T]ATGTTTCAGGAATAA | 10213 |
rs553134295 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324633 | GATTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTG | 10213 |
rs553152268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362625 | TTTAAAAATTGAGTA[C/T]AAAATTCTTTACTTT | 10213 |
rs553189813 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378433 | GGATATTTTTCTTTT[C/T]CTTTAAGGAAAAATA | 10213 |
rs553192172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360116 | AGGACTATGTGGCTC[A/G]TGGAATGATTTAAGC | 10213 |
rs553255258 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369182 | TGTTCTTAGGCTTTA[A/T]TATCATTACTTCCAT | 10213 |
rs553258315 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358715 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCATGAGA | 10213 |
rs553276816 | snp | A/C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336654 | GATCTTGGCTCACTG[A/C/T]AACCTCTGCCTCCTA | 10213 |
rs553293302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390696 | GGGAATTCCAGATTA[A/G]TGTGGGTAAAGAAAC | 10213 |
rs553299252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380508 | AAGTAAATTATGCAA[A/G]TTACACCCCATCCCC | 10213 |
rs553325513 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363146 | ACAGTATTTTGAACA[A/C]CTATGTGAGGGATCT | 10213 |
rs553327667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375291 | ATACTGATAACCTAC[A/G]TTGCATACTGATACA | 10213 |
rs553371345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330940 | CCCTAGTGTTGTAAA[C/T]GGAGCCTGAGTTATT | 10213 |
rs553373507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322885 | CATTCTAGTTTCTTA[A/G]TTTTCTCTAAATAGG | 10213 |
rs553406215 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375834 | CCCAGGAGTTTGAGA[C/T]GAGCCTGTGCGACAT | 10213 |
rs553448495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314454 | ATCATTTTGTCCATT[C/T]GCAGTGTGCCATTAC | 10213 |
rs553496857 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390011 | CTGGGATTACAGGCT[C/T]GAGCCACTGAGCCCG | 10213 |
rs553502357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365401 | CAGGCACTTTTCTAA[A/G]TACTGGTTATATATA | 10213 |
rs553509069 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161381231 | AATAATTTTTATTAT[A/G]TATAATATATAGGTA | 10213 |
rs553512167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315147 | TTATCCCCCGGGGAC[G/T]TTTGGTAAAGCTTGG | 10213 |
rs553574491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330365 | AGACATTGCAACATA[A/G]TCTCAATATTCCAAA | 10213 |
rs553578758 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339889 | TCCATTAAATGAAAA[C/G]ATTTTCTATAAACTT | 10213 |
rs553596506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310304 | TGTTATTGTTATTAT[A/C]TTAGAAGTGGAAGAG | 10213 |
rs553598196 | in-del | -/GTTTA | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371928 | ACCCCTTTTGTTCTT[-/GTTTA]GTTCTCTTTCTCTTT | 10213 |
rs553605469 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397000 | ACCCAGCTAATTTTT[A/G/T]TATCTTTTAGTAGAG | 10213 |
rs553648684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393821 | AAGAAAAACCGTCTT[A/G]AAATATAAACTTGAA | 10213 |
rs553687954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385911 | TAACTATTATCATTG[C/T]TTGATTAGTAGGTAT | 10213 |
rs553726198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332980 | ATATCTCACCCCCTT[A/G]AATAAGTGTATAAGA | 10213 |
rs553756163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326776 | GCTCAAGTCCCTTAG[A/G]TAAAATGGCATAGTA | 10213 |
rs553782562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366275 | CCACTTTGAACAAAA[A/G]TAAATAAAAACAAAA | 10213 |
rs553802923 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311166 | ATACAAAAATTAGCC[A/G]GGCATGGGGGCGTGT | 10213 |
rs553840508 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161319783 | TTGTTTCAGACTTCA[C/T]GAAATTTTCAGTGTT | 10213 |
rs553850453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317831 | GTAATAATACCATTT[C/T]CTTAAGCATACACTT | 10213 |
rs553879621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397360 | GGCACTGGTCGGATA[A/G]ACGAAGTGAAAGAAG | 10213 |
rs553914715 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322808 | TCTTAGTTGTTTTAT[C/T]TGGGAGTTGTAGTAG | 10213 |
rs553915687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318465 | ATTGAAGGAAATTCA[A/G]TCATACATATGATAA | 10213 |
rs554010916 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333561 | GACACTAGCTGAGAT[C/G]CATGGAAGAGGAAGA | 10213 |
rs554023416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389188 | GTATCTGTGAGTCCA[G/T]TAACTGGCTTCTGTA | 10213 |
rs554034362 | in-del | -/TTT/TTTT/TTTTT | 0.144632 | 0.226711 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357076 | ATAATGGCAAATGCC[-/TTT/TTTT/TTTTT]TTTTTTTTTTTTAGC | 10213 |
rs554100531 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396704 | TTAAGAAACAATATG[A/C]TTGGCTAGCATGCAT | 10213 |
rs554121786 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359434 | TTTTTAAAAAGTCTC[-/A]AAATGCTTTGTGTAA | 10213 |
rs554123785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326273 | TGACCTCAATTGATC[C/T]GCCCACCTCGGCCTC | 10213 |
rs554126839 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376255 | ACCTAATTTTCTTGA[A/G]CTTCAGATTTTTCAT | 10213 |
rs554159195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404536 | CCCTCTCCCTTCCTT[G/T]AGGCTAACTGGATAA | 10213 |
rs554188347 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382284 | TCAACCCCTATTTTA[G/T]TCCTCTGTTTTGATC | 10213 |
rs554219841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388442 | TCTTTTATATTATCA[C/T]TGGAAATTTAATTAA | 10213 |
rs554250989 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161377097 | GCTAGAGTTCAAGTT[C/T]AATAGTCATTTGTCT | 10213 |
rs554287917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358704 | AATCCCAACACTTTG[A/G]GAGGCTGAGGCGGGT | 10213 |
rs554295984 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353551 | ATCTTCCCAGAATGC[A/C/T]TTTTCCCTCCCTCCC | 10213 |
rs554311494 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161325568 | ATGGATGAGGACTCT[A/G]TATCACCACATGCCA | 10213 |
rs554312172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319483 | CTGCCTCAGGATAGT[C/G]TATCTGCTTTCAGAT | 10213 |
rs554313948 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377444 | CAGATCTTGTGAGGA[C/T]AGCTAAGAAAATATT | 10213 |
rs554356724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161377336 | GAGCATACCCTTCCA[A/G]GGTATTCTTGGAACA | 10213 |
rs554386600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334000 | GGCGCCACTGCACTC[C/T]AGCCTGGGACAGAGC | 10213 |
rs554438797 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386165 | CCTCTTGAGTGATTG[A/T]TTTCTTTGTATCATT | 10213 |
rs554471302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342238 | AGGGGGAAACATTCA[C/T]TATCTGACCATCAAA | 10213 |
rs554522828 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357020 | AAATTTGTTAAAAGG[-/C]CTGAGTAGGTAACAC | 10213 |
rs554623393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312884 | GTAATGTGAAATATG[C/T]CCAGCATTTTGAAAC | 10213 |
rs554638087 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357837 | CGTTTATTCTAATAG[G/T]TATTATTAAATGACC | 10213 |
rs554649010 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331562 | CGCGCCTGGCCTCTT[C/T]GGATATTTTATAGCT | 10213 |
rs554671498 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389788 | GAAAGAACATAGGCT[A/G]TGGAATCAGAATGAC | 10213 |
rs554698743 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365706 | ATTATATATATTGGT[-/G]GGGGGTGATGTTTTG | 10213 |
rs554710654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311876 | CGCCTCGGCCTCCCA[A/G]AGAGCTGGGATTACA | 10213 |
rs554713356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405536 | TGTTTTAAGGATTCA[A/G]TAAATTAATATTTGT | 10213 |
rs554745226 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321550 | CAAGTTAAAGGCTCA[C/G]TTCTCCACAGAACTA | 10213 |
rs554828646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318572 | AAAGTTTTGAAAGTA[C/T]GCTAAGATTGCTTGT | 10213 |
rs554835839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406637 | GGCATTTGATTTGGA[A/G]TATCTTAGAATTGAA | 10213 |
rs554896317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351932 | ATGTGCCTGAGAGAG[A/C]GGAACCAGAAATATT | 10213 |
rs554919204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389249 | GACCACCATGTAGGG[C/T]TGTGCAAGTAGTGAG | 10213 |
rs554938821 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323041 | AAACCAAAACTCTAC[A/T]GCATACTGCCATTAA | 10213 |
rs554956271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378584 | AATGGATATTCAGTG[A/G]CGAATGAGACACAAA | 10213 |
rs554971589 | in-del | -/ATG | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383471 | TGTTTTTAACAGATC[-/ATG]ATATCTACTGAACTA | 10213 |
rs555025645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315962 | TTCTCCTGCCTCAGC[C/T]ACCTGAGTAGCTGGG | 10213 |
rs555026396 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161341481 | TCTCCCAGTACATGG[A/G]CTTGTCTTTTTATCT | 10213 |
rs555028981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392452 | GAGTTGGGCTCTCCA[C/T]GCTTACCCCCTCTTT | 10213 |
rs555047793 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329330 | AGTCTTTTTTTATAT[A/C]TGTCACATCTGTCAT | 10213 |
rs555050346 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161328716 | TTCTAATTTTATTTA[A/T]ATTTATATGGTTATA | 10213 |
rs555062314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320470 | CATTGTGTCCTTAGT[C/T]TGTACTCTTTTTTGA | 10213 |
rs555083529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330278 | GGATTTATGACATCT[A/G]ATACCATTTTTGGTA | 10213 |
rs555123217 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310676 | AATTGCTTTGGACGT[-/A]TTTTTACAACAGACT | 10213 |
rs555183453 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406501 | CATTTGTTTCTGCTG[C/T]AATCATTTCTTACGT | 10213 |
rs555233185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401018 | CCATTCTCAGTTAAG[A/G]AAGTTGAATTGCTTG | 10213 |
rs555235256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410469 | TCTATTGTGTATAAT[A/G]TATATTCCTTATTTC | 10213 |
rs555238724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343030 | CCATGATTTATGTTC[A/G]TTATTTTTGTCTAAA | 10213 |
rs555240162 | in-del | -/A | 0.00087489 | 0.0208969 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385429 | TATCACTTGCTTTTT[-/A]AAAAAAAAATTGACT | 10213 |
rs555270452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354982 | TCAGTAGGCCTAGGA[A/G]AAGAAACTTTTCAGA | 10213 |
rs555275368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334838 | AAAGTGCTGGGATTA[C/T]ACAGGCATGAGCCAT | 10213 |
rs555411232 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341023 | CCTCCGCCTCCGCTG[G/T]CGCCGCCGCGGGATC | 10213 |
rs555420359 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332858 | AGTAATTTTGGTTGG[A/G]GATCTGACTGGCACA | 10213 |
rs555450156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341985 | CAGAAGTTTTATAAT[C/T]TTTAAATGTCGCATT | 10213 |
rs555450164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333635 | TAGGATCTTGTTCCT[A/G]TTCTTCTTCCAGAGT | 10213 |
rs555486884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384380 | CAGTAATACTTATTA[C/G]AAGCAGAATTTTCAG | 10213 |
rs555585544 | in-del | -/TTTG | 0.00993419 | 0.0697739 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391581 | AGTTGTGTAGTGCTT[-/TTTG]TTTGTTTGTTTGTTT | 10213 |
rs555610585 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310025 | AATCAGCCGGGCATG[A/G]TGGCACGTGCCTGTA | 10213 |
rs555611086 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394441 | ACTGAGGATCAGAAA[C/G]ATTGACACAAGGTCA | 10213 |
rs555647644 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309293 | TGTGTCTGTCAAAAG[A/T]AAAAGAATGTAAACT | 10213 |
rs555671652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338581 | CATTCAATAACTTTA[A/T]AATACTTTTTGAATT | 10213 |
rs555671714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347035 | TCAGTAATCTCAGCT[C/T]TGTCATCTCAACTCA | 10213 |
rs555745745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357097 | TTTTTTTAGCACTTA[A/G]TCAACAAGGGCTACC | 10213 |
rs555765349 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348932 | TAGAAAAAACATTTG[C/T]TCCTACTCCAGGTAG | 10213 |
rs555865682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384604 | TGATAAATCTATTGA[A/G]TTAAATTCCCTTAAA | 10213 |
rs555891733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403399 | TGGGCAAGGCAGGAA[C/T]GGGGAGGTAACAGCT | 10213 |
rs555958037 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311044 | AGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 10213 |
rs556020441 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364653 | GAAAACAACAGCCTT[A/G]GTCACTGCTGGCTGA | 10213 |
rs556042363 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326447 | TTAGAACTCTTGTAC[A/T]TTGATGGTAGAAATG | 10213 |
rs556051045 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337774 | GTGCTGTAGCAGGAA[-/G]GGGGATTAGACTATG | 10213 |
rs556057538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365232 | GTTAGTATGTTTCTG[A/C]ATCAGAAGAAAGGCC | 10213 |
rs556084729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393791 | AATTGAAGAAAATTT[A/G]TAGGGTAGGACTTTA | 10213 |
rs556178991 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359817 | TGAAAATGGGATGGC[A/G]TACTGTACTGGAAAG | 10213 |
rs556200190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317509 | GTTTCTGAGGTGCCA[A/G]TAATGTTCTGTTTCT | 10213 |
rs556215744 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334092 | AATCCTAGCACTTTG[G/T]GAGGCTGAGGTGGGC | 10213 |
rs556240978 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333493 | TCACTATGAAAGGCA[G/T]TATATATTGGGCAGT | 10213 |
rs556279542 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326249 | TTGGCCGGGCTGGTC[C/G/T]CGAACTTCTGACCTC | 10213 |
rs556292625 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161411741 | GAGATCTTTTTGGCA[A/G]TGGGTGGGATTGATG | 10213 |
rs556393284 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334653 | GGGAACAGATGTGAC[A/C]ATGTTGATGGAAGAA | 10213 |
rs556509916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332932 | TTTGGCAAGTTTCTT[A/T]GCACTTTCCCATTAA | 10213 |
rs556510418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366104 | TGTTATTACTTTACT[G/T]TAGCAGAGTTTTCAT | 10213 |
rs556513951 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342009 | TCGCATTTTTGTTTG[C/T]GATCCATTTTGAATT | 10213 |
rs556529960 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380952 | TAAGCAGTTGATAAC[A/G]GGTCATTTCTAGGTG | 10213 |
rs556551852 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379126 | ATTGCTTTGCTTTAT[A/G]TGGAATTGGCAACAG | 10213 |
rs556560281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342095 | TGCATGTGGATATCC[A/G]GTTACTACAGCACCA | 10213 |
rs556607575 | snp | C/T | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395686 | ATACATGTATACATA[C/T]AGATTGCAACTCATT | 10213 |
rs556614260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337525 | AGACTTGGTCTTTCT[A/G]ATTCTAAAGTATCTC | 10213 |
rs556641895 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398606 | GGTGAAAAAATGAAT[C/T]GTGAAGAACATTTTA | 10213 |
rs556655239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408422 | GATTGATAAGAAAAA[A/G]GGAGACAGAGAAATG | 10213 |
rs556672210 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396641 | AGGTTTGGGTGGAGC[A/G]GGGTGGGTTGGGAAG | 10213 |
rs556718558 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345807 | TATTTTTTCTGCTTA[G/T]AATTGTAGATGGCTT | 10213 |
rs556763150 | in-del | -/AC | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399383 | ATATTTTTACCTATA[-/AC]ACAGAGTGAGCTAGT | 10213 |
rs556787379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365265 | TGACATGTGGCTTGC[C/T]TCCTCTCTCTCGAGG | 10213 |
rs556804449 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382683 | ATATTCCTGAAAATA[C/T]TCTTCATACTTTAGC | 10213 |
rs556819593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349951 | GATTAAAAATATGAT[A/C]TGTATAACATTGAGA | 10213 |
rs556902739 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401332 | GAGGAGAGTCAAAGT[A/G]ACATACAGATTTTCA | 10213 |
rs556903624 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386702 | TGTTTAGCCTTGATA[A/G]TGACCTTTCTTATAA | 10213 |
rs556913909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344814 | CTGCTCATATGATTT[G/T]CAGATATTATCTCTC | 10213 |
rs556924247 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408950 | AATAACATGTTCTTA[G/T]AGAGTTAAAACTGTT | 10213 |
rs556933126 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345491 | CAAGCAATCTGCCGA[-/C]CTCAAGCAATCCGCC | 10213 |
rs556963904 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342300 | CTCTTTATCAGGTTG[A/C]AGAAGTTCCCTGCTA | 10213 |
rs556964419 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355182 | ATAAAGAAATATATC[A/G]TTGGTTAAACTTACT | 10213 |
rs556993838 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346295 | TAAAGTTTTGTCATG[C/G]CTCTCTGAACTCACC | 10213 |
rs557003512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400243 | CTCTCTGCTCTGCTT[C/T]CCTTGTGTTGGCTTT | 10213 |
rs557180810 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352946 | TTCAGCTCCTTTGAT[A/C]AGTGATCCAGCTAAT | 10213 |
rs557180886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331549 | AGGCGTGAGCCACCG[C/T]GCCTGGCCTCTTTGG | 10213 |
rs557206570 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410719 | CATTTTAGAATTGAT[A/C]CAAATTGTATTTAAA | 10213 |
rs557249191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361691 | GTACAAAGATGATTT[A/G]ATAGTGGGAAATATT | 10213 |
rs557254111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407720 | TATCCAAATCTAACC[C/T]TCACTGGGATTTTGG | 10213 |
rs557290379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381911 | TATTTCCAAGAGTTG[C/G]AATTAGTAAAGCAAC | 10213 |
rs557306554 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373002 | AAAGAATGCATTCTC[A/G]AAATAGAGTAAATAA | 10213 |
rs557325797 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371991 | TTTTATTTCTTTCTT[A/T]CTAGCCCCATATGCC | 10213 |
rs557348279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315283 | AAAATTATCTGGTCC[C/T]GAATATCAGTAGTAC | 10213 |
rs557366163 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315744 | AATATTCCATACTAT[A/T]TGATAGATTTGTAAT | 10213 |
rs557368936 | in-del | -/TGAGCATTACTGCC | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363062 | TGAGCAGCAGGCAAG[-/TGAGCATTACTGCC]TGAGCTCCACCTCCT | 10213 |
rs557392862 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161408753 | TGAATGAAAATTCTG[A/G]TCATCATTATTTTTG | 10213 |
rs557430410 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307826 | CGATAATTACATGGA[A/G]AAATGTGAATAAATG | 10213 |
rs557472473 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400277 | CCTTTAGGTCACCTC[A/G]TGATTCATTGTGATT | 10213 |
rs557481259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322954 | TTCTTGGATCTCGTT[C/G]TCTTGACACACTGCA | 10213 |
rs557495668 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161308390 | CTCCAATTGGCCGTC[A/G]GGGAACGGAAGCCGA | 10213 |
rs557506972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338434 | TGCCATTGATAACCT[A/G]TATTTGTTGAGCTGC | 10213 |
rs557509891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380790 | CTCTGAATTTTTTAT[G/T]CTGTGGGCTTACAAG | 10213 |
rs557546062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331679 | TGTGAATAGGGAATG[C/T]CATTGTAACATCTAG | 10213 |
rs557580587 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375074 | TTAATCTGATCAAAA[C/T]ACTCAATGGACTTTA | 10213 |
rs557593129 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406720 | AATCTACAGCTGCTC[C/T]TCATTTCCCAGATGG | 10213 |
rs557628093 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331814 | AAAAGGACTGATGCT[C/G]AGTACCTTCCTTATT | 10213 |
rs557643586 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396804 | TGTCAGGATAAGAGG[-/T]TTTTTTTGAGGAGTT | 10213 |
rs557656348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324606 | TTTCCCCTAGGTGTT[A/G]TAGTTTCATGAAGAT | 10213 |
rs557680639 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383080 | CGGTGGCATAATTAA[A/C]ACCTTCTTCACCCAT | 10213 |
rs557706951 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306725 | TGGACATCTTATTCC[C/T]CAGCTAAATACTTTA | 10213 |
rs557718894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356287 | CATTGAAGCTCATGC[A/G]GTAGAAATAGTTTAC | 10213 |
rs557719153 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392004 | CTAGATTCTGATCCC[A/G]TTTTATACCAGTTTT | 10213 |
rs557747528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401534 | GTTATGTTACAGCAG[A/C]AGAAGGGGAAGATGG | 10213 |
rs557755425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356953 | TTGGCTAAATAATTG[A/G]TACCAGTTCACACTA | 10213 |
rs557797984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391703 | CCCAAGGGATCCTCA[C/T]TCTACAGCCTCCCGA | 10213 |
rs557798416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347808 | GGTACTCTTCTAAGT[A/G]CTTTAAATATATTAG | 10213 |
rs557803326 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409139 | ATTTACTAGGAACAA[A/G]TTAGGACACTTGTAT | 10213 |
rs557835366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348701 | TATAAAGAAATGCAC[A/G]ATCACTAAGATGAGA | 10213 |
rs557849839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332274 | TAGAGGTTACAAATA[A/G]TACAACTTTTAAAAG | 10213 |
rs557882158 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324643 | TCTTTCTTTTTTTTT[G/T]TTTTGAAGTATGAAG | 10213 |
rs557894236 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314926 | TGGGGCATATACCAA[C/T]GAGTGGAGTTGCTGG | 10213 |
rs557898040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322614 | GGGCTGGTCTTGAAC[C/T]CCTGACCTCAAGTGA | 10213 |
rs557925497 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382308 | TTTGATCTGTGAGTT[A/G]CGCATAGACCAAAGG | 10213 |
rs557976063 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340154 | GAACCTCAGTGAAAA[G/T]GTGTCTTAGCAATGA | 10213 |
rs557996569 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402682 | TGAAAAGAAAGTATA[A/C]AAGAATTAAAAACAG | 10213 |
rs558015098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354129 | ATGAGACGTTCAGGT[G/T]CTGCTTGATTCTGGG | 10213 |
rs558030930 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408534 | CTCAGGTACTTCCAT[C/T]TCCCATCTCCTGAAG | 10213 |
rs558045253 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394324 | GGCTTTTCATCCTGA[A/C]AATAAGGAAGTTTTA | 10213 |
rs558047611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345994 | CTTCCCAGGCTTAGG[C/T]GATCCTCCCACCTCA | 10213 |
rs558051975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354928 | CTCAAAATACTGGCT[C/G]TAGGGCCACCAAACT | 10213 |
rs558118314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363745 | TCACAGGGCATTCGA[C/T]TGGGATGTGGCCTGC | 10213 |
rs558142730 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161308515 | GCCGCGTCGGGTGTG[C/T]GCCGCTGCTGCTGTT | 10213 |
rs558169716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309177 | TATCATACTAATTGA[A/G]TAATTGTTGGTAAAT | 10213 |
rs558261415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368615 | TCTACCTTCCAAAAA[A/G]AGCACATATATCCTT | 10213 |
rs558272608 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161411988 | TTATAAACATACTTT[C/T]AGGATTTTGGAAGAG | 10213 |
rs558382876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374243 | TCTTCAGCATAAGTC[A/G]GGGGAAAGAGCTGTA | 10213 |
rs558465325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347253 | CTTTAGGTGGGAATG[C/T]AGATTTAGTTTCTGT | 10213 |
rs558525104 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378385 | AGACTATATTGTTAA[C/T]AAGCTACTGATTAGA | 10213 |
rs558544197 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380285 | CACCATACTGACTAC[A/T]TGCATATGTTGAAAA | 10213 |
rs558576703 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161328097 | TGGTTAAAGTCACTT[C/T]GGAGAGCAATTTGAC | 10213 |
rs558653705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406873 | TAAAATTTGAATTAG[C/T]GCTTTTTATACCTAA | 10213 |
rs558666469 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363704 | TGATCTGTAGCTGTG[-/A]AATGGGAAAAGTTCC | 10213 |
rs558756158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314218 | GTGTGAACTGCATCA[A/G]CATCATAAAACATCA | 10213 |
rs558763362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388342 | CATTTAGTACATGAG[A/G]AAACCTGAGGCCCAT | 10213 |
rs558771797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367686 | TTATAAAAGGAGTTT[C/T]TATTTTCACTGGAAC | 10213 |
rs558791564 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311997 | TGTTGACTCACTCAC[A/G]ATCTTCCACTGGAAA | 10213 |
rs558798720 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405917 | AGAGAGATACAGGGT[G/T]GCAAAAGCAAAGGCT | 10213 |
rs558816571 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161364177 | TGCTGGTTGATAGCC[A/T]GCCTGCGTGCTGGTT | 10213 |
rs558837896 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373959 | ATCCTAAAGATAGGC[C/T]CTGTTACCATTACAT | 10213 |
rs558894871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399137 | TAAGTGTGTATGACC[G/T]TTGTGAAGAAAATGA | 10213 |
rs558925326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344497 | TATGAATAGGAAGGA[A/G]GGGGCACAAATATTC | 10213 |
rs559033282 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360841 | ACGCCTGGCCTTCGT[A/T]TTTATTTCATCATGT | 10213 |
rs559070519 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312419 | AGAGTGCTGGGATTA[C/G]AGGCATGAGCCACTG | 10213 |
rs559081341 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330306 | GTAGAAAGTATATGG[A/G]AAAGAAGACAGAAGA | 10213 |
rs559153729 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336003 | ATGAAAGCCCTACTA[C/T]TATTACTTGTTTTAT | 10213 |
rs559169798 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408248 | TGGAGTAGTTTCAGA[-/T]TTTTTTTCTGAATAC | 10213 |
rs559175308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397795 | CCTGATTATAGTGTT[G/T]CAACTGGAAATCCCC | 10213 |
rs559209766 | in-del | -/T | 0.155325 | 0.23138 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342333 | CTACTTTGTTGAGAC[-/T]TTTTTTTTTTTATCA | 10213 |
rs559217746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389322 | AGCTCCACTCTCTAC[A/G]CCAGACTATGTCTGC | 10213 |
rs559306488 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330297 | CCATTTTTGGTAGAA[A/C]GTATATGGGAAAGAA | 10213 |
rs559306995 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359438 | TTAAAAAGTCTCAAA[A/T]GCTTTGTGTAACTTA | 10213 |
rs559313338 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307612 | GTAGATTCATCACCA[C/T]TCTCGATTTAGGAAT | 10213 |
rs559331543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335074 | GCCTTTTATGCTTCT[A/G]ATTAACAGAATTCAG | 10213 |
rs559369475 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161328324 | AATGAACTAGGTTCT[A/G]TATACCAATATGCAT | 10213 |
rs559395607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388812 | ATCCGTAAGCCGTGT[A/G]TTTTATAATGCACCT | 10213 |
rs559437189 | in-del | -/AAATC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391407 | GAGGAAGTAGGAAAT[-/AAATC]AAACGTTCCACTTTG | 10213 |
rs559507229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353380 | TTGCTTATTTGAAAA[C/G]TCACATCCTCAGAAA | 10213 |
rs559531051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379496 | TCTTAAAGCGTCACT[C/G]TCTAATTTCCTATTT | 10213 |
rs559666768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369838 | TTGGTTCAATTATTT[C/T]GTATTTCTGGTAAAC | 10213 |
rs559701160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405953 | AATAGAAGAGAAGAC[A/G]GATGTTGGAGTAGCT | 10213 |
rs559755469 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161330663 | GTCTGGGTTGAGTGC[C/T]CTGAAAGTATGCCAC | 10213 |
rs559815956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399886 | AATTTCACAAAAACA[A/T]ACAGAAATATCTACA | 10213 |
rs559843713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345150 | TCCTCATTTAATTGT[C/T]TTGGTCCCTTTGTTA | 10213 |
rs559942643 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320821 | CCCTCTGCCTCCTGG[C/G]TTCAAGTGATTCTTC | 10213 |
rs559944206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358035 | AAAAAAGACTTTTTT[C/T]CCATTACTTTTTTTT | 10213 |
rs559987589 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403955 | CTCTGTTGCCTAGGC[A/G]GGCTGCATGATACTA | 10213 |
rs559999791 | snp | A/T | 0.000488438 | 0.0156199 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385430 | TATCACTTGCTTTTT[A/T]AAAAAAAATTGACTT | 10213 |
rs560007153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403007 | AAAAAGTTAAACAGA[C/T]AGTTCCCATATGAGC | 10213 |
rs560015664 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332860 | TAATTTTGGTTGGGG[A/G]TCTGACTGGCACAGG | 10213 |
rs560043740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360448 | GCAACCTCCACATCC[C/T]GTGTTCAAGCGATTC | 10213 |
rs560064521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374661 | ATATTTTAAACTTTA[A/G]TTCTCAAGTGGCACA | 10213 |
rs560107782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321821 | TGCAGAGCTCCTGTG[C/T]CCTCTCTTCATGGAA | 10213 |
rs560116188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357478 | AACAAACTTATTTTC[A/G]AGAGTCAGAATTACT | 10213 |
rs560170399 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389527 | AGTAAGGATTTAATA[C/T]ACACTCTTGGTACTT | 10213 |
rs560195569 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311459 | TTAAAGTATATAGGA[A/G]GATGTGCATAGGTTA | 10213 |
rs560233737 | snp | C/T | 1.8026e-05 | 0.00300211 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318819 | TTTGTTTCTGTTTTC[C/T]AGAAATATGGACAGA | 10213 |
rs560248340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161348344 | CATTGTAGTGCTAAA[A/G]CAGCCATATATTACA | 10213 |
rs560302635 | in-del | -/CA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366421 | ACACACACACACACA[-/CA]AAAGCACAAAGTACA | 10213 |
rs560327769 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327131 | AAAAGACAAATGTTA[A/T]ATGATTCCACTTACA | 10213 |
rs560352884 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317482 | ATAGACTGGAAGCGG[A/G]GCTTGGGTGGCGTTT | 10213 |
rs560429749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325059 | TCACATGATTTCACA[C/T]TGTGAAATTCTGTGT | 10213 |
rs560460438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325658 | TCATGGAAATAGGCA[A/G]ACTGACTCTAGAATT | 10213 |
rs560461656 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316867 | GATTTTCTTTCTCTC[A/T]GCTTCTTGCATCACT | 10213 |
rs560470638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316090 | CTCAGGTGATCCGCC[C/T]GCGTTGGCCTCCCAA | 10213 |
rs560483677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375726 | AGAATAAATACAAAT[A/T]CAGGAAGAAAGTTAG | 10213 |
rs560519806 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348621 | TATACGATTGTTTTT[A/G]TGTACAATTTTAAGA | 10213 |
rs560607722 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161409694 | GATAACTGAGGGAAG[C/T]GTGTTACCAATTCAC | 10213 |
rs560681524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404730 | TCTTTCAGTTATTTT[C/T]CTTGTCCTCTTGCCT | 10213 |
rs560696713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341329 | CCGGCGCCTCCATCG[C/T]GCCGCGGCCGCCGAG | 10213 |
rs560718336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374775 | ACTTGTAATGTGACT[A/G]TACTTCTTTCTTGAG | 10213 |
rs560744948 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161407660 | TACATGTTCATTGTT[C/T]GCACATGAAGAAATT | 10213 |
rs560758363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364983 | GTGACATGCCCCTTG[G/T]AATCCCAGCACCTCA | 10213 |
rs560783926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350164 | GTGTAAGGAACTTAG[A/G]ATAGAAAGTACTTGT | 10213 |
rs560806075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333761 | TATTTTGCCAGGTGT[A/G]GTGGCTCACGCCTGT | 10213 |
rs560894726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365524 | TTTATTTCCCTTTTT[C/T]TCTAAAAAAAAATAT | 10213 |
rs560900528 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311588 | AAATTAGGAGACTCC[A/G]TAATAGATTATTATG | 10213 |
rs560922375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358130 | TGGTTTATATCATTA[C/T]ATAATTTTTTTAACC | 10213 |
rs560963344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349252 | TCTAGCCTCTCATTT[A/G]TTATGCCTTTTGGAT | 10213 |
rs561042745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317919 | TGTTGTCATTTTTAA[A/C]TTACTTAGTTGTACT | 10213 |
rs561063913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312287 | TAGCTGGGATTATAA[A/G]CACCCGTCACCACGC | 10213 |
rs561080649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319708 | TCCCACATTTCCTTA[C/G]TGCTATCAGTGACTT | 10213 |
rs561106182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161377458 | ACAGCTAAGAAAATA[A/T]TATAGGTACTAATTT | 10213 |
rs561144639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310390 | CAATTTTGTAGTAAC[A/G]TTCATTTAATAATTC | 10213 |
rs561211345 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332638 | AATGATGAGGTTTCA[A/G]GTATTACACTGCTTA | 10213 |
rs561275147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368076 | CATTAATCTTTAAAA[C/T]GCAGCATAACTTCTT | 10213 |
rs561302979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314872 | TGGTGTAAACATGCA[C/T]GTACATGAACTTATT | 10213 |
rs561468473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388550 | CTCTTTTGCCTTCTG[C/T]AACTCAGTTCTCCAC | 10213 |
rs561501468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334384 | TGACTGCCTGGCCAC[A/G]GTGTCTTTTTTGTTC | 10213 |
rs561502363 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400537 | AAAACCTCAAACTGC[A/G]TAGCCCAGAATTATT | 10213 |
rs561513345 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324134 | TGTCAGTGGCATTTA[A/G]TAACTTGTCTTCAGT | 10213 |
rs561524029 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161399659 | CAAATGGTGTATAAA[C/T]ATGGAAAAGTTCTAG | 10213 |
rs561616907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319017 | TATTGATGTTTGTTA[C/T]CTTGCAACACTAGAT | 10213 |
rs561640361 | snp | A/C/G | 8.9683e-05 | 0.00669588 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371353 | TCTTTATTGCCATCT[A/C/G]CTGCCACATTCTGTT | 10213 |
rs561667379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376757 | TCATCTGTCTGTGTT[A/G]TCTTCCCCACAAGAC | 10213 |
rs561676617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372408 | GCTGTTAAAATACGG[A/G]GTTTTTATCTGTCAT | 10213 |
rs561709681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309592 | TAATGGTGGCCTTCC[C/T]GTCACGTAAGGCTAC | 10213 |
rs561741473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339703 | CAGCCTGGACAAGGG[C/T]ATGACTATTGCTGTT | 10213 |
rs561778257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340316 | AAGTGGGGTTCCCAG[A/G]GAAAAGGGTCGGCTG | 10213 |
rs561810489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363227 | CATCTCAAAACCATC[C/T]TCCCTGCCCCAAAAC | 10213 |
rs561832202 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380434 | TCATTAAAGCATATA[C/T]GTTCAAAACTTGTGG | 10213 |
rs561843618 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345269 | TTTTTTTGAGACAGG[G/T]TCTTGCTCTGTCACC | 10213 |
rs561861216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337064 | AATCTTTTAAAAACC[A/G]TTAACCAAGATGTTT | 10213 |
rs561895922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337756 | TTGCAGTAATTGAGA[G/T]GATGTGCTGTAGCAG | 10213 |
rs561924616 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383731 | AATGATGCTTTGCTC[C/T]TAAATATTTACTGTT | 10213 |
rs561960808 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313033 | GTTAAATGTTTTTTT[G/T]TGTGTCCATTGTTTT | 10213 |
rs561969680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346679 | TTTGCTTTTAACCCT[C/T]GCTAGTTAAGACTGG | 10213 |
rs561978291 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343271 | CCACTTTCTGTTTGT[C/T]ACGAATCTCACTATT | 10213 |
rs561984629 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388279 | GTTTCAGTAATTACT[C/G]AACATATAAGTTATA | 10213 |
rs561987848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161308650 | TGGGGAGGCAGCCGT[A/G]CTAGGCCGCCGCCAG | 10213 |
rs562012312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325162 | GGGTATATAATGCCT[G/T]TAAGTTGTCACTTTG | 10213 |
rs562017379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402789 | ACTTGGATAGAAATT[A/T]CCCAGAGAAGATATG | 10213 |
rs562036548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383748 | AAATATTTACTGTTA[A/C]CAGTTAGGGTGGCAA | 10213 |
rs562044786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391878 | TGCTGCAATCATTAG[C/T]ATGAGCCATTGCACC | 10213 |
rs562094584 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161308229 | AGAGCGCAGAGGTAG[C/G]GAGAGAAAAAGGAGG | 10213 |
rs562124456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355635 | GGAATTTGGACTTTT[C/T]TGGCAACCAATCATC | 10213 |
rs562220895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325852 | TACATCCATCAATAT[A/G]TGGGAACTTGGTTTG | 10213 |
rs562364247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161411098 | TCAAGCTTTCATTGT[A/G]TAATCTATTATTTTA | 10213 |
rs562368783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347261 | GGGAATGTAGATTTA[C/G]TTTCTGTTACTCTAT | 10213 |
rs562385524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401956 | TGTGTTTCCTTATCT[C/T]TAAAATGAGGTTAAG | 10213 |
rs562456523 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316024 | TTTTTTTGTATTTTT[A/C]GTAGACACAGTGTTT | 10213 |
rs562485940 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364122 | CCACTGGAGTCAGGA[C/T]GCTGTCCTCCAACTG | 10213 |
rs562521709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364835 | ATGGCTGGGTGCAGT[C/T]GCTCACGCCTGTAAT | 10213 |
rs562523660 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356415 | AGTTAGTTGTATGTG[C/T]TTGAATTCATTTATG | 10213 |
rs562580923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326004 | AAAATTTGTACCAAA[C/T]GGATTGAATATCTAA | 10213 |
rs562595084 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349212 | GTTTTATAAGTATGC[A/G]TCAAATCCTAATAGT | 10213 |
rs562616395 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161308698 | TCACGTTGCCCAGCT[G/T]AGTTGCCACAGGAGG | 10213 |
rs562702250 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338726 | TTTTGACTGTATTTA[C/T]TCAGGAAACCATCAC | 10213 |
rs562709874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331835 | CTTCCTTATTCTGAT[A/G]TGAAGTATTTATGCA | 10213 |
rs562741832 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392500 | TTTTTAATCTAATCT[A/G]TATGCTGGGGGGGAG | 10213 |
rs562746903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332479 | TAATAATGAAAAAAG[A/G]GGTACAGAGAGCTGT | 10213 |
rs562752931 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366986 | AGCTTCATTAGGTGA[C/T]ATGCAGAGGATGTTG | 10213 |
rs562782691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324877 | ATTTTGCTTTGACCA[A/G]TGGAATGTGATTGGT | 10213 |
rs562834770 | in-del | -/T/TT | 0.499703 | 0.0121769 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360191 | ATATATATGCATGTA[-/T/TT]TTTTTTTTTTTTTTT | 10213 |
rs562835848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385031 | TGTCATTTCAAGTAC[C/T]GTGGTGGTGTAATTG | 10213 |
rs562842643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383528 | GTTTCACACCTGCTT[A/C]TAATATTTCAGAGAA | 10213 |
rs562843223 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394580 | TATTGAGCTATTATT[A/C]GATATTGTTCTAGAA | 10213 |
rs562903008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402005 | GTATCTGGCACATGA[C/T]AGGCATTTAATAAAA | 10213 |
rs562929768 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347302 | CATAAGCAGATGTCC[C/T]TTTTGTCTACTTTTA | 10213 |
rs562945869 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353457 | AGGAATCCACGCTTT[A/G]GTTAGCTCATTTTAT | 10213 |
rs562964787 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339833 | GAGAAGGCCACTGGG[A/G]ATGCATGCCATAGGG | 10213 |
rs562980495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329880 | GATTATTCTGAATAC[C/G]TATTAAACTCTGTGA | 10213 |
rs562982305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336850 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG | 10213 |
rs563006980 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333933 | CTACTTGGTAGGCTG[A/T]GGCAGGAGAATGGCC | 10213 |
rs563016806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330418 | GATACAATCTGTGTT[C/T]TCTTTCCCTACCTTC | 10213 |
rs563028795 | in-del | -/AGA | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397465 | AATTTAGGTAGAAGT[-/AGA]AGGATTGAGGAAGGA | 10213 |
rs563038263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375630 | ATTCTTTTTTCCACA[A/G]ATATTAGAATGTAAA | 10213 |
rs563042654 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341061 | CCTTCGGGCTCCCCC[A/G]GTCCCGCAGGCTCCC | 10213 |
rs563065573 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357294 | GGTTTGTTTGCCTTT[G/T]CAGAATTCATAACAG | 10213 |
rs563193974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402976 | GCCACTGTGGAAAAC[A/T]GTTTGGTGGTTCCTC | 10213 |
rs563204102 | in-del | -/CCTCCCAA | 0.00398564 | 0.0444627 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314001 | CCAGAATTTTTTCAT[-/CCTCCCAA]TTGCAATATTTTTGA | 10213 |
rs563209582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394041 | AGTGGCGTGACCTCA[A/G]CTCACTGCAACCTCC | 10213 |
rs563226245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322148 | GGGTTTTTGAGGCTC[C/T]GTGCCAGAAACTCAG | 10213 |
rs563245686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399378 | AGAAAATATTTTTAC[C/T]TATAACACAGAGTGA | 10213 |
rs563261471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389416 | ATATGAGCACAGATT[A/G]AAGGAAGCCCTGATC | 10213 |
rs563280462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390104 | GAAGATTAGAAGATG[C/T]AATGTGTAAAGCAGA | 10213 |
rs563282723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379747 | GCAGTGAAGGGTTGA[C/T]CATGCAAAGGAGAAA | 10213 |
rs563298437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379070 | ATGCTCTACTGCCAT[A/G]CTAACAAAGTTGAGC | 10213 |
rs563347063 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377341 | TACCCTTCCAAGGTA[C/T]TCTTGGAACAAGTTT | 10213 |
rs563360975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352404 | TACTTTCTGGGGAGG[C/T]GCTTTGAAATAGGGC | 10213 |
rs563395499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344006 | CTATTTGAATAGCAT[C/T]TACATTGTATTAGGT | 10213 |
rs563431914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406095 | CAGTGTTTGTAAAAG[A/G]GTAAATAAAGTGATG | 10213 |
rs563440645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400608 | ACTCAGTCTGGAGTA[C/T]AATAGCATGATCATG | 10213 |
rs563460267 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410842 | TGATTTTTGCTATTA[C/G/T]AAAACATAGAAGAAG | 10213 |
rs563474904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401121 | GATAATGTAAACTTA[C/T]TGTATTGATAAATAA | 10213 |
rs563476853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391373 | ACATTTCACCTTATT[C/G]GTAGGTGCTGAAGTG | 10213 |
rs563495682 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408637 | TGTATTTCTTGTCTG[A/T]TTTCAAAATGATGAT | 10213 |
rs563560095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346163 | GCTGGGATTATAGGC[A/G]TGAGCCACCGTGCTC | 10213 |
rs563594960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361926 | TTTATATGTTTTCAT[A/G]ACTAATATATTTGAT | 10213 |
rs563607860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161398222 | TGATTGAAAGAAATA[C/T]GGTGGGTTTTTTTAG | 10213 |
rs563648015 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388294 | GAACATATAAGTTAT[A/C]AAACAATTGCACTAG | 10213 |
rs563650637 | in-del | -/TAAT | 0.00438332 | 0.0466095 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341918 | TATATTTTGATATGA[-/TAAT]TAAGAAATCTCTCCT | 10213 |
rs563697483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322258 | ATTTGAATTTTTCTT[A/G]TACTATGATACTGAT | 10213 |
rs563735618 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406154 | GAAACTTGACCATTA[C/G]CAGAAAAAAGAGAAT | 10213 |
rs563777862 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161407838 | CCTTAAATTTTCTTG[-/T]TTTTTTTTTCCATTT | 10213 |
rs563947755 | snp | A/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306974 | GGGGAACATGGTGAA[A/T]TCCTGTCTCTACTAA | 10213 |
rs563959066 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406285 | TGCAGACCGTGCATG[A/T]TGGGATAGCCATCTG | 10213 |
rs563984630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327247 | ATTGTTTAATGGGTA[C/T]GGAGTTTCAGTTTAG | 10213 |
rs564024501 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349572 | TCTATTTAAGATGTT[C/T]GATCAGGTAACAGAT | 10213 |
rs564043279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330594 | TTTAAAACCCAAGCA[C/G]GTAGGACTGATTCTC | 10213 |
rs564045751 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379904 | TAGGTTCTAGTACCA[C/T]TGCTGTGTTCAGTTG | 10213 |
rs564045843 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391245 | TTAAACTATTACCTG[G/T]TATGTGATTTAAATT | 10213 |
rs564078921 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407837 | ATCCTTAAATTTTCT[A/T]GTTTTTTTTTCCATT | 10213 |
rs564170048 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347168 | CAAATTTTGGAGATC[A/G/T]TTGTTCTTTGTTGCT | 10213 |
rs564260179 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161316003 | CCTGCCACCACGCCT[A/G]GCTAATTTTTTTGTA | 10213 |
rs564299750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344047 | ATCTAGAGATTATTT[A/G]AAGTGTATGGAGGAT | 10213 |
rs564331202 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408343 | AGTGGATCAAAAGTC[A/G]GTAGCTCCTTTGATC | 10213 |
rs564333512 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345868 | TTTCATTTTTCTGTT[A/G]CTACATCTTCAAGTT | 10213 |
rs564354672 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354462 | GTTGCCCAGGCTGCT[C/G]AATGATGTTTTTTTA | 10213 |
rs564397152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390216 | TCTATTAGTTAGAGA[A/C]GTGGTGGTTATTTTG | 10213 |
rs564413337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392051 | TTAACATTACCTGAC[A/G]TTTTGATGAATTAGC | 10213 |
rs564451425 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161384166 | AATCTTTGGGAAAAT[A/G]TTAACTGTTCAAAAT | 10213 |
rs564498750 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362078 | TTTTAATTAAAAAAA[A/T]TTTTTTGAGACAGGG | 10213 |
rs564526679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350550 | AGACAGACAGATAAA[A/G]TGTTATTATAGTTGT | 10213 |
rs564565437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351723 | ATACTGTATGTCTAC[A/G]TGGGTCGTCTGGGTG | 10213 |
rs564593112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401819 | TATCAGTGAAAAGTA[A/G]TGATTTCCCCAATTG | 10213 |
rs564606412 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404377 | TTTTCTACCAAAAAT[C/G]TAACTTTATTAAGTG | 10213 |
rs564607636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332589 | ATGTTTCCAGACTAG[A/G]GCATCATAAATGGCA | 10213 |
rs564629998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392736 | TGTGTACCACAGTTT[A/T]CTTCTGCTGTGATAG | 10213 |
rs564637319 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396307 | AAATGAAATCAGTAC[A/G]TTGAAGAGATGTATG | 10213 |
rs564718633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362924 | TTGCCTTTGTTTATT[G/T]TTTCTGTTTATTTTA | 10213 |
rs564722464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365639 | AGGAATAATTTTATG[A/G]ATACAGTGTTCGTTA | 10213 |
rs564751432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358295 | TCATGTGATCACTTA[G/T]TCCATTTTAGTTGAA | 10213 |
rs564783034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409893 | ATATCACCCTTGTTA[C/T]CTTTTCCACTACTTA | 10213 |
rs564785462 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401837 | ATTTCCCCAATTGCC[A/G]TGAATGTTTCTTTGA | 10213 |
rs564812092 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307884 | GGCTTAAAATAGGTG[A/G]TTTGAACATTTGGGA | 10213 |
rs564828409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405768 | TTGTGCTGTCTTATG[C/T]AAAAATTGCCATAAT | 10213 |
rs564910500 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161376533 | AATATGGTAATGACT[A/T]CAAAAGAAATGAAGA | 10213 |
rs564921398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342445 | TCTTTTTTATTCCTT[A/G]TAACAATTCTTTGCT | 10213 |
rs564949950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366691 | TGCACTAATTGTGGG[A/G]CAGAATCACATTTAT | 10213 |
rs564958825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334400 | GTGTCTTTTTTGTTC[A/G]CTAAGGTTTGTGTGT | 10213 |
rs564997686 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320978 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 10213 |
rs565055304 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161355232 | CAGCAGTGGGTGAAA[C/T]TATGTCTTTATTGTC | 10213 |
rs565061355 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323588 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGC | 10213 |
rs565094442 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326797 | TGGCATAGTATTTGC[A/G]CATAACCTAGACACA | 10213 |
rs565100936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388660 | ATTTAAAGGATATCA[A/G]TTACCACCGTATTTT | 10213 |
rs565136005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310539 | CTTTGGTGACCTTAT[C/T]TGTGAAATGGGAGAA | 10213 |
rs565138575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389303 | TGAGGGAGCTTCCAG[C/T]TCAAGCTCCACTCTC | 10213 |
rs565194525 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358024 | TTAAGCACCAGAAAA[A/G]AGACTTTTTTTCCAT | 10213 |
rs565293664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360283 | CAGCCTTGACCTGGG[C/T]TCAAGTGATCCTCCC | 10213 |
rs565316489 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358381 | ATGTTAACAGTTTCT[A/C]CTTGTGAAATCTTTA | 10213 |
rs565330157 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360961 | TCATAAATGGGAAAA[C/T]TATTTTTTCAGGGTG | 10213 |
rs565472597 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354062 | CACTATAAGAACTCT[A/G]AAGCCAGTTGCAGTC | 10213 |
rs565479447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378614 | ACCTTGCTGTTGAGT[A/G]TAACTGAACCTAGTA | 10213 |
rs565518031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161328275 | TTTAAATGTCTAAAT[A/G]TGTTATGATGAAATT | 10213 |
rs565521079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349774 | CTGCTGTGAGCCAGA[C/T]GAGCAGGGTGGGGTT | 10213 |
rs565534272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334481 | TAATCAATAGGTTTC[C/T]CTTTACAGGTGAGGA | 10213 |
rs565540827 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382003 | ATATTTTCAGAAAAA[C/T]AAAGGGTTATATAAA | 10213 |
rs565557565 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312375 | TCTTGAACCCCTGAC[A/C]TCAAGTGATCTGCCC | 10213 |
rs565564530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320760 | AGATGGAGTCTCACT[C/G]TGTCGCCCAGGCTGG | 10213 |
rs565596927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342587 | GTTTCTTGTAGGCAG[C/T]GTGTAGTTAGATTTT | 10213 |
rs565773217 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311847 | CTCAAACTCCTGACC[G/T]CAGGTGATCCAACCG | 10213 |
rs565809963 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319336 | ATAGATGGATTAATA[A/C]GTAATCTCTCTCCTT | 10213 |
rs565921292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339026 | GATATATAACACTTT[A/G]TTTATCCATTAACTT | 10213 |
rs565928742 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368431 | TTTTTTCCCAGGCAT[A/G]GTATTTTGTTTATAT | 10213 |
rs565933570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373609 | TCTCCCTTTTCCTGC[A/G]TGTGATTTATCAAAG | 10213 |
rs565945039 | snp | A/C | 9.76896e-05 | 0.00698822 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395217 | AGGTAAAAGTTACTT[A/C]TGCCATTTCTTCTTT | 10213 |
rs565958119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405031 | ACATGTTCATTACTT[C/T]AGATGCTGCTGTTCA | 10213 |
rs565984642 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387026 | CAAACCTGTGTTAAA[C/T]AACATGTGTATGTAA | 10213 |
rs565996806 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161334725 | CTTTAAGTATTTTTC[C/T]TCTGATGTGTTTTCT | 10213 |
rs566020578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161398560 | TTTAATTTTGATAAT[A/G]TTTGATTACATATTT | 10213 |
rs566021463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397471 | GGTAGAAGTAGAAGG[A/G]TTGAGGAAGGAGGTA | 10213 |
rs566046077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352545 | TTTTCTGTCTCCTAT[A/G]TTACATTTTAAGGAC | 10213 |
rs566051702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406470 | CCTAGTGAGGACACT[C/G]CCTGTGCCTGAATTT | 10213 |
rs566059421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389622 | AAGAATCTATTGTTA[A/G]AGTACTCATCTAAAA | 10213 |
rs566099406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344172 | CCCAAGGGTACTGAG[C/G]GATGACTATACTCAG | 10213 |
rs566103387 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335618 | GATTTACTTAATTAG[C/T]GCTCTACTGATATAC | 10213 |
rs566148632 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405932 | GGCAAAAGCAAAGGC[A/T]AAGGGAATAGAAGAG | 10213 |
rs566149415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359777 | AGTGAACTAAGCTCC[A/C]AGAATAAAAGTAGAC | 10213 |
rs566152447 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359440 | AAAAAGTCTCAAATG[C/T]TTTGTGTAACTTAGA | 10213 |
rs566185084 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345509 | CAAGCAATCCGCCCA[C/T]CTCTGCCTCCCAAAG | 10213 |
rs566232530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312437 | GCATGAGCCACTGCA[C/T]CTGGCCAAAAATTGA | 10213 |
rs566366319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339188 | GGACCATATGGTAGG[C/T]ATATGTTTAACTTCT | 10213 |
rs566435354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410430 | CAATAATCGTAAGAA[A/T]ATAATCATTTAAATT | 10213 |
rs566520940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340045 | CTAACTAATCTATCA[A/G]ACTTTCTAAGAAAAG | 10213 |
rs566522813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362455 | GATTTCTTTATATGA[C/T]GACTCTTCCATTTTT | 10213 |
rs566632009 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372612 | TTCTTGCTATATGCC[A/T]ATATTTCAATTTATT | 10213 |
rs566644035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310781 | GTGAGTAGGTGGTGA[C/T]GCCGGATTCAAATTG | 10213 |
rs566718849 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161385385 | AAACAGATGCACGTC[A/G]ATCATGCCTTGTCCA | 10213 |
rs566756104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325388 | TGTATGGATTTTTTG[C/T]ATATTCACTAATAAC | 10213 |
rs566816381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309964 | GCCTGGCCAAGACTA[A/G]CCTGGCTAACATAGT | 10213 |
rs566820289 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355916 | TCTATCTTCTTTTCA[G/T]TGTTAAAATAGGCAA | 10213 |
rs566832730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365129 | CAAAAATAAAACAGC[A/G]CTCATACAATAAACA | 10213 |
rs566854478 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161316529 | TTGTCAAACTCAACA[A/G]ATTGAAGGTTAACAC | 10213 |
rs566856516 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161381279 | CATTATATATATAGT[C/G]AGCTGACTTGAGGTT | 10213 |
rs566881731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403051 | CATAAGTATATACCC[A/C]AAAGAATTGAAAATA | 10213 |
rs566901145 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358391 | TTTCTACTTGTGAAA[G/T]CTTTAGTTTCTTATT | 10213 |
rs566905413 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394116 | AGCTGAGATTACAGG[C/T]GTCTGCCACCACACC | 10213 |
rs566912533 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343653 | CCCAACATGGTGAAA[A/C]CCTGTCTATTCTAAA | 10213 |
rs566975195 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310704 | ACTTGCAAAGTAGAT[A/G]TTATCCCCACTTTAT | 10213 |
rs567018387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394158 | TGTGTTTTTAGTAGC[A/G]ACAGGCTTTCACCAT | 10213 |
rs567109927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393558 | GTACCACAAATAGCT[A/G]TAAACTTCTAAGCAA | 10213 |
rs567114318 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363136 | AGGAGCACAAACAGT[A/G]TTTTGAACACCTATG | 10213 |
rs567167514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374288 | TTTCCATAGTTTTCT[A/G]TAGGTATTATGTATT | 10213 |
rs567193138 | in-del | -/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306782 | ACAAAGTTTAAGGGT[-/T]TTTTTTTTTTTTTGA | 10213 |
rs567206562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375079 | CTGATCAAAACACTC[A/G]ATGGACTTTAAAAAA | 10213 |
rs567250704 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359649 | GTGTTCTCTGTTCTC[A/C]GTGAGCATACTAACT | 10213 |
rs567294025 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340650 | CAGGATCCTGCTAGC[C/T]AAGGGACAAGTCCTG | 10213 |
rs567327411 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356014 | ACTCTTCTCTTCTGA[A/C]TAATATAGTCATTGA | 10213 |
rs567330803 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333409 | GGGGTCAAATTCATG[G/T]CCCATGTCACTTTTT | 10213 |
rs567385081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385401 | ATCATGCCTTGTCCA[C/T]TGTTGCTTGGCATTA | 10213 |
rs567496356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311811 | GTAGAGACCAGGTTT[C/T]GCCATGTTGGCCAGG | 10213 |
rs567606428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350997 | GTGTCCTCCTTTGTC[C/T]AATCTCCCTTAGTAA | 10213 |
rs567643496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310028 | CAGCCGGGCATGGTG[A/G]CACGTGCCTGTATTC | 10213 |
rs567674416 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306510 | GTTGAAATGACAAAA[A/C]CGCAATTTTTTGCAC | 10213 |
rs567726436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386523 | AATCTTCATCAAAGT[C/G]AAGTGTTTTGTTTTA | 10213 |
rs567748302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161404249 | TTTTACAGCTAGTCT[A/G]TAAGCTCTGTGAATT | 10213 |
rs567816718 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354185 | CAATCTTAAATGTTT[A/G]TATTTTCTGGTTTCT | 10213 |
rs567827023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375125 | ACTGCAGGTCAGCTT[A/G]TCTGCAGGTATTTCT | 10213 |
rs567865515 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365234 | TAGTATGTTTCTGAA[A/T]CAGAAGAAAGGCCAC | 10213 |
rs567880727 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321846 | ATGGAATTAGGGCAT[A/G]TCACCCTCCCTGCAC | 10213 |
rs567903660 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161319083 | TTCTCCTGGGAATAA[G/T]AATTTTCTGTTATTT | 10213 |
rs567935104 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361451 | CAAAATTGAAAAACA[C/T]GGATAGATTTTTTTT | 10213 |
rs567953999 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394326 | CTTTTCATCCTGACA[A/G]TAAGGAAGTTTTAAG | 10213 |
rs567971865 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353644 | CCAATAGATTGCTGT[C/G]ACTTATGTGTGTGTT | 10213 |
rs568005112 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314036 | TGAAAACATTGAGAG[C/T]TCATAATTTTGTTGA | 10213 |
rs568118676 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372936 | TATGATATCTTGACT[C/G]ATGTGATGGTGGCTA | 10213 |
rs568199675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316123 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 10213 |
rs568218661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379321 | GAGTTCAATTTTAAG[C/T]TCACTGTTTATTTGT | 10213 |
rs568256103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363545 | ATAGTTTTCTAAAAT[G/T]TTGTTCATGATTCCT | 10213 |
rs568278955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330698 | GCAGGGCAGTGGTCT[C/T]CACTGGGCAGCCTCT | 10213 |
rs568340781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338218 | CAAGAATCCTTGGAA[C/G]TATATTTAGAGCTAT | 10213 |
rs568358196 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369212 | TGTAAATGCTTGTTT[G/T]ACAATATAAAATAAA | 10213 |
rs568396772 | snp | A/T | 6.34136e-05 | 0.00563052 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370101 | TTTTCTTTCTTTCTA[A/T]ATCAGGGTGTCAGTG | 10213 |
rs568454087 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336046 | CATTATAAGCCTAGA[A/G]GCGTATGTTTAATGC | 10213 |
rs568464209 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378548 | TGCACTGTATTTTGT[A/G]TGCCACTTACTCTGT | 10213 |
rs568477318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324587 | ACTTGGTGATTTTTA[C/G]TTTTTTCCCCTAGGT | 10213 |
rs568558435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316203 | AATGTCTGTCTTCAA[A/C]GTTAGTGTTCATGAG | 10213 |
rs568572879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408577 | GTTTGCAAATGGTCA[A/G]CACAATCATTTAGTG | 10213 |
rs568619487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331515 | TGCCTGCCTCGGCCT[A/G]CCAAAGTGCTGGGAT | 10213 |
rs568626032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400835 | ACAGGCATGAGCCAT[A/G]GCACCTGGCAGCCCA | 10213 |
rs568690620 | snp | A/G | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381780 | TTGGGCATGCTTGGA[A/G]TAAATACGGAACTCA | 10213 |
rs568761404 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161409695 | ATAACTGAGGGAAGC[A/G]TGTTACCAATTCACT | 10213 |
rs568764603 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401356 | ATTTTCACCTGTGAC[A/G]GGTTAGCACCCATAA | 10213 |
rs568796753 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307410 | CGGGGCTACTCACCC[C/T]CTCCTCCCATAAAAA | 10213 |
rs568810617 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338369 | TTTTTGGAAAGAAAA[A/C]CTTCTCTTAAAATTT | 10213 |
rs568845659 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354848 | ATAATGGTGTCATTT[C/T]CCCCTCTCCCCTGCT | 10213 |
rs568914972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364492 | GCCAGGGGCCACACC[C/T]TCCTCTACCCAGCCC | 10213 |
rs568924218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370258 | TATAGATGTTTATCA[A/G]TGTCATTTCTAGAAA | 10213 |
rs568998934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381455 | AGAGAGAGAAAAAAA[C/T]TACAGCTACTGCCAG | 10213 |
rs569035753 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371455 | TTTACTTAAAAAACA[A/C]AAAAACTGTACAAGT | 10213 |
rs569049303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356916 | ATGTTTAATCAGCAG[A/G]TATTTTAATAACATA | 10213 |
rs569096206 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347143 | GGTAAGGCTCACCTC[A/G]TTTGTTTCCCAAATT | 10213 |
rs569158166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315027 | AGTTTGAGAAAATTA[A/G]TCTAGGGTATTATCA | 10213 |
rs569171565 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386623 | TGAAATAAGCTACCA[C/G]TGGTTTTGATTGGGT | 10213 |
rs569173586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332715 | AACATACTGATCCCA[G/T]TTATGAATTCTGTGG | 10213 |
rs569173600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324624 | GTTTCATGAAGATTT[G/T]CTTTCTTTCTTTTTT | 10213 |
rs569212581 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362347 | ATTTCTCCCTCCTGC[C/G]TATATAGTTACCTGG | 10213 |
rs569239245 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309812 | ACTTTGGGAGTTTTT[G/T]GTTTTTTGTTTTTTT | 10213 |
rs569247643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389921 | TTTTTTTAGAGATGG[G/T]GTATTGCTATGTTGT | 10213 |
rs569247657 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344070 | TGGAGGATGGGCATT[G/T]GTTATATGCAAATAC | 10213 |
rs569275624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317120 | TTTAATATTATAAAA[A/T]ATACAGGATTCCCCC | 10213 |
rs569285999 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314059 | TTTGTTGAAGATAGG[A/G]TGGCCATCTTTCCTT | 10213 |
rs569289877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365063 | GTGAGCCAAGATCGC[A/G]CCATTGCACTCCAGC | 10213 |
rs569315702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368531 | CCTTTTTGTTTGATG[C/T]ATTAGACTTGTGTTG | 10213 |
rs569363754 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161327695 | ATGAAGACAGGATAC[G/T]GGCAACACATTAATC | 10213 |
rs569422430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339080 | TTGGTTTTTGGCTGT[C/T]ACAGATAAAACTGCT | 10213 |
rs569435560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392266 | TTTTTTAAAAGAACA[C/G]TGAGTTTACTGTTGA | 10213 |
rs569437926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383106 | CCCATTGCTCATTAG[C/T]GCACTGGACATTAAT | 10213 |
rs569448277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315777 | TGTACAATTAACCTA[C/T]ACAGTAATGACATGA | 10213 |
rs569454970 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369097 | GTCTTTTTATATTAG[A/G]CTACATGAAACACAT | 10213 |
rs569512517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331305 | TCTCACTCTGTTGCT[C/T]GGGCTAGAGTGCGGT | 10213 |
rs569513574 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320030 | CTCAAGAGGCCTAAG[A/C]CTCTTTGAACTTGAT | 10213 |
rs569517579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378362 | CAGAACTGAGCAGTG[A/G]TAAGTAAAGACTATA | 10213 |
rs569560044 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383963 | TGATAGTACTTGTTT[G/T]TATTGCTTTTTTAAA | 10213 |
rs569569440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393142 | AGCCTTACTCGAGGG[C/T]CGCAAGGGAATCCTT | 10213 |
rs569575788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161335178 | TGTTACTTCAGAATA[C/T]AAATGGGCACATGTT | 10213 |
rs569675237 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389876 | TTGTGTCTTATTTTC[G/T]TTCTTTTTTGTTGTT | 10213 |
rs569720610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313190 | TCTGACTGTAGAGTC[A/G]TAGTACTTGACTCTC | 10213 |
rs569827270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396551 | CCAAATACCACATCA[C/T]CTCACTTATATGTGG | 10213 |
rs569895615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360630 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCTACTG | 10213 |
rs569921190 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342672 | TAATTCAGATATTTA[A/G]GTAATTTACATTTCA | 10213 |
rs569932200 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319485 | GCCTCAGGATAGTCT[A/G]TCTGCTTTCAGATCA | 10213 |
rs570013707 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394636 | AATAGGGCAAAGTCC[C/T]TGCCTTCTTGATTTC | 10213 |
rs570023406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345384 | AGTAGCTGGGACCAC[A/G]GGTGCATGCCACTAT | 10213 |
rs570075091 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161334549 | TATTAAGACATTTTT[A/T]AAAAAGTGCCTTCAG | 10213 |
rs570079031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380099 | ACTACAGTGGCAGAA[A/G]CATATATATTATTTT | 10213 |
rs570090637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337257 | ATTCCTAAATTTAGT[A/G]TTTGTTTCTAAATCA | 10213 |
rs570108453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370273 | ATGTCATTTCTAGAA[A/G]AAGTGGTTATGTAAT | 10213 |
rs570128300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330755 | GTGATTGCACAGGCT[C/T]TTCCCTTCAGCAGAC | 10213 |
rs570204087 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344373 | GTTGTAGACTGCTGG[C/T]TTCTTGTTGTATCCT | 10213 |
rs570238514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407364 | TTTGGCATGTTATTA[A/C]CTTTTTCTTCTTTCG | 10213 |
rs570264869 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337543 | TCTAAAGTATCTCTG[C/T]ACCTAATCAATATTT | 10213 |
rs570310304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313235 | ATAGTCATTAGTCAT[C/T]GCCATTTACCATCTA | 10213 |
rs570324678 | snp | A/G/T | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369151 | GGTACTTATGTAGAT[A/G/T]CCCATTATAATACAT | 10213 |
rs570326015 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161325259 | ATCCCAGAAGGCTTC[C/T]TGAATGTGGTGAGAT | 10213 |
rs570352439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408005 | ATTGGGAGAGGAGGG[C/T]AGTAGTGGTAGCCAA | 10213 |
rs570380424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330010 | TGTCAGTTTGTTTGA[A/G]TATTTTAATTGTGAT | 10213 |
rs570431806 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390455 | TCAGGACATCCAGGA[C/T]TATTGTTTCTTAATA | 10213 |
rs570439736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369963 | CTTGATTGGTATGAG[G/T]TTTATAATTGAATGA | 10213 |
rs570445812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320315 | TGGAAATCCATGCTG[A/G]AAAACCCCTGGACAT | 10213 |
rs570482704 | snp | A/T | 0.00358779 | 0.0422022 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161316504 | GCAAGAGCTTTCTTT[A/T]AGAAGACATTTGTCA | 10213 |
rs570509662 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306429 | GAGGGGTTTAGTACT[A/T]ACGTTGGGACAAGCC | 10213 |
rs570536028 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376714 | ATGAGGTGATTAATG[C/T]ATTGCACTTAACCAT | 10213 |
rs570547832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313962 | ATATTCACAGTGTTA[C/T]GTAACTGTCACCACC | 10213 |
rs570577947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161398456 | TATTAGACATTTGAT[G/T]TTTTTCTAATTACTG | 10213 |
rs570647377 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382879 | CCCCTACCAACCCAT[A/T]CATTAATTAATTCTT | 10213 |
rs570655010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336363 | TATGGCATATTGGTC[A/G]GAAACAAGGAAATGA | 10213 |
rs570696000 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391630 | AGGGTCTTGCTCTGT[C/T]TCCCAGACTAGAGTG | 10213 |
rs570750328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161330811 | CTTAGGGACAATAGA[C/G]TAAATAATAAAAATA | 10213 |
rs570759194 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389468 | CAGTATAGCATTTTT[A/G]TGCACTAAAATTTAA | 10213 |
rs570759226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378422 | TTATAGATAATGGAT[A/G]TTTTTCTTTTCCTTT | 10213 |
rs570764745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346206 | TTTTTGTTAAATCTT[C/T]TATTAACCCCATCTA | 10213 |
rs570798008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379147 | TTGGCAACAGGCAAA[C/T]GAGTTGTTTTAATTT | 10213 |
rs570829101 | in-del | -/TTAAC | 0.00676609 | 0.0577691 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318541 | AATAAGAAAATATAA[-/TTAAC]TTAATGATAGCAAAG | 10213 |
rs570856752 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343451 | CCATATTTTGTTTGT[C/G]CATTCATCTATTGAT | 10213 |
rs570857090 | snp | C/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307355 | AAAGAGGCAAGTGTT[C/T]ATACTCTTAAGTTTC | 10213 |
rs570890956 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380453 | CAAAACTTGTGGATT[C/T]ACTCTTTGAATTTTG | 10213 |
rs570892494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371614 | TACTCAAAGCCTGCT[A/G]TAAACATTTTATTAA | 10213 |
rs570926386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323429 | AGCCCTTTGGGAGAC[C/T]GAGGGGGCAGATGAC | 10213 |
rs570963094 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161324466 | GAGTTTTGAAATATG[A/T]GTCAAGGCATATTCA | 10213 |
rs570992102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339165 | AAATACCTAGGATTA[C/G]ATTGGCTGGACCATA | 10213 |
rs570996775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408134 | TCATGTATTGTTTGG[A/G]TTAATTTAATTTTGA | 10213 |
rs571008954 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386677 | TTCCAAGAGAATATA[C/T]TATTGGACCTGTTTA | 10213 |
rs571033971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400113 | CAAGTAATACTTAGA[C/T]CTAAGGTTGTGTTAG | 10213 |
rs571080222 | in-del | -/TAGT | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342591 | CTTGTAGGCAGCGTG[-/TAGT]TAGATTTTGAGATGT | 10213 |
rs571086172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357733 | TTTTCTATTGTCAGT[A/G]ATGTGTGTGCTTATT | 10213 |
rs571098885 | snp | A/C | | | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161412147 | AGCCACAGAAAGTAT[A/C]TGTCTAAAAAGCAAA | 10213 |
rs571099745 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161329109 | TAGAAAATTCTCTTC[G/T]GAGTGAGTTGGGAAG | 10213 |
rs571102087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408698 | TCTGAAGTTTAGCAT[A/G]ATTTTATTTGTTCAG | 10213 |
rs571112880 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333928 | CACAGCTACTTGGTA[A/G]GCTGAGGCAGGAGAA | 10213 |
rs571148781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341658 | TTCTGACTAACACGG[G/T]GAAACCCCATCTCTA | 10213 |
rs571165426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349442 | AAACTGCATTTATTT[A/G]TAAAGAGATTGAAGA | 10213 |
rs571184967 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333883 | TAAAAATACAAAAAT[G/T]AGCCAGGCATGGTGG | 10213 |
rs571254255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333522 | GTGGTAAAAACCCAG[A/G]GCTCTGGAGTTAGGC | 10213 |
rs571292660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326259 | TGGTCTCGAACTTCT[A/G]ACCTCAATTGATCCG | 10213 |
rs571331551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161326746 | GGACCTCTGATGATA[C/T]CAAAATCTATGGCTG | 10213 |
rs571334281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347792 | CACTCACTGTGTGCC[A/G]GGTACTCTTCTAAGT | 10213 |
rs571425403 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161355753 | ATATTAAGGATTCTT[G/T]TATAGACATTATGGG | 10213 |
rs571441128 | in-del | -/AA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336979 | GGAAGTTCTTTTTTC[-/AA]AAATTTACACTTTCA | 10213 |
rs571474472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340751 | TGGGGTTTCCATTTT[A/C]TCTCTCAAGCTTTTA | 10213 |
rs571494595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403165 | ATCAGTAGATGAGTG[A/G]ATAAACAAATTGAGG | 10213 |
rs571503706 | snp | A/C/T | 1.80585e-05 | 0.00300482 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318903 | TCTTGAGCATTTCCT[A/C/T]GTGTGTAAACTACAA | 10213 |
rs571559831 | in-del | -/TTTG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396820 | TTTTTTTGAGGAGTT[-/TTTG]TTTGTTTGTTTGTTT | 10213 |
rs571592423 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403563 | AATGCAAATTGGTTC[A/T]TGTCACTACCGTGCT | 10213 |
rs571664520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397266 | GAGCTTGCTACTACC[C/T]AAACAAAAGGTACGA | 10213 |
rs571669201 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361218 | ATTTAGTTTTAAATG[-/C]TTCCAGTACTAAGAA | 10213 |
rs571686068 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161351869 | TTGGCTGAAGAGGGT[C/T]ACATGTTCATACCTA | 10213 |
rs571691366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396664 | TTGGGAAGGTGTTGG[A/G]GAGCAAAAAAGACAT | 10213 |
rs571750507 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367143 | ATGCTTTAGTTAATT[G/T]TGCTAGTCCAACAGC | 10213 |
rs571776818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366127 | GTTTTCATTCTGAAA[C/G]AGATCTTAGCTATTT | 10213 |
rs571814309 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392860 | AAATTCATTCAGAAT[A/G]TAAATATTTTATCAG | 10213 |
rs571819819 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335324 | TGTGGGTTGGAAATA[C/T]ATTATATTTAGCTGC | 10213 |
rs571829088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161319145 | TATCAAAGTTGGCTT[C/T]TAGGAAAAAAAAACC | 10213 |
rs571871947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358634 | CTCATACGTTTTTCT[C/T]CTTAAGTTTTTTCAT | 10213 |
rs571990545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386024 | TCTTCTTTAAAAAAC[C/T]CACCTTTAAAATAAA | 10213 |
rs572037084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310328 | GGAAGAGATTAATCT[A/G]GTCCTCTTATTTCAG | 10213 |
rs572042672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366318 | GAGAAAACTTATTCT[A/G]GAACCTTTTATACTT | 10213 |
rs572103754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358038 | AAAGACTTTTTTTCC[A/G]TTACTTTTTTTTATA | 10213 |
rs572190749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333064 | GTGAAATGACTTTAG[C/T]ATCTGTCTTGTACAT | 10213 |
rs572191037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394414 | CAAGCCCCTTAATTC[A/G]TAGATCTCTAAACTG | 10213 |
rs572305667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161388462 | AATTTAATTAATTAA[C/T]TTTGGCATAGAAAAT | 10213 |
rs572397714 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161328627 | AATTCTAAGTGTTAT[A/G]TTACTTAAATTTAAA | 10213 |
rs572415705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361115 | ACCAATATTTTTGGC[A/G]TAGCATTTGTTACAC | 10213 |
rs572449375 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161334851 | TATACAGGCATGAGC[C/T]ATCACGCCTGCCGTT | 10213 |
rs572451208 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320136 | AGTAATAGTGTTCAG[A/G]CATGTGAAAATGTGA | 10213 |
rs572463527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329203 | ACTCTGAAGATGAAG[C/T]TACCACAATAATGTT | 10213 |
rs572477144 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326722 | AGTATCCTCGGGGGA[C/T]TGATTCTCGGACCTC | 10213 |
rs572601113 | snp | A/G | 1.84626e-05 | 0.00303825 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367910 | TCAGGAACAGTGAGT[A/G]CTTTTATGGTTGCCT | 10213 |
rs572650876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161350106 | TGGTATGTTTAGTAA[C/T]ATAAAGTTGCCTTTG | 10213 |
rs572687959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342254 | TATCTGACCATCAAA[C/T]ATGATATTAGCTGTA | 10213 |
rs572739136 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315468 | GATTTCTTAACTGTG[A/C]TAAATGAAAACTGAA | 10213 |
rs572767246 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409153 | AATTAGGACACTTGT[A/G]TCCTGAATTAATTTT | 10213 |
rs572778538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161338436 | CCATTGATAACCTGT[A/G]TTTGTTGAGCTGCTG | 10213 |
rs572816899 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331765 | TTTTCCTCTGGAATT[A/T]AAAAAAAATGGGGTG | 10213 |
rs572826012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161342849 | GTTGAATTTCTAGCT[A/G]TAACTTGTTTTGTTA | 10213 |
rs572831349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392361 | AGCAAATAAGATCAT[C/T]CTATCTAGCCCAAAC | 10213 |
rs572838903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391748 | AGGCATGCACCACCA[C/T]ACCTGGCTATTTTTT | 10213 |
rs572914089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161347856 | ACTCTTTGCAGTTTG[A/G]TTATTGTCACAGTGC | 10213 |
rs572956368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161382421 | ATTTAACAAGCCTGA[A/G]AAATTATAAACTATC | 10213 |
rs572992679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372245 | AAATAAAATCACAAT[A/C]TATTTATGCAATCCT | 10213 |
rs572994590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383229 | GACTATATTGCCATG[C/T]TTATATTTTATTGCA | 10213 |
rs573049563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354161 | CCCTCTTTCCAGTTA[C/T]GTTTTTGCCAATCTT | 10213 |
rs573105461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315350 | ATTAGAGACTAGAGT[A/G]CTATAATCTGTCTCC | 10213 |
rs573124606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356993 | TGGAGTAATATAACT[A/G]ATAGTGTTAACAAAT | 10213 |
rs573220195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346487 | CAGTTGACTGACTTA[C/T]CTCCTTACTGTGGGC | 10213 |
rs573262238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161403265 | ATGGACCTCTAAAAC[A/G]TGGTAAGTGAAAGAA | 10213 |
rs573305808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161393827 | AACCGTCTTAAAATA[C/T]AAACTTGAAAACTTA | 10213 |
rs573348991 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161340266 | TGTAATCAATATGGC[A/G]TCTCACCCCCGACAA | 10213 |
rs573433935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161373328 | TGTAAATATCTATCA[C/T]TGATGATTTGTATCA | 10213 |
rs573451293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309209 | GATTACATTTCTCGT[G/T]TTAAGTAAAGTAGAA | 10213 |
rs573509941 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336685 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCT | 10213 |
rs573512088 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161308527 | GTGCGCCGCTGCTGC[C/T]GTTGCCTCTGTCTTC | 10213 |
rs573534618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383350 | TAGTGTAAAGTAGTC[A/G]TTTTCTATAGGCCAT | 10213 |
rs573549230 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410596 | AAGCCTCCTTTTTAA[C/T]TCAGTCTATTTCAAA | 10213 |
rs573585487 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161401605 | TTTCCAACAACCTTA[A/C/G]CTACAGTTTCTCTTA | 10213 |
rs573588223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410983 | ACAGGTATACATATA[C/T]AAATGAAATTTTTTA | 10213 |
rs573616510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325453 | AAATGTTGTTTCAAT[A/T]GTTTGTCTCAGGTTT | 10213 |
rs573644700 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384422 | TTTGGTTGGCTTAAC[A/T]ATTTTTAATCTCTTA | 10213 |
rs573673763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340397 | CTCATTCCTCAAAGT[C/G]TTCTGTGGTTTGGCT | 10213 |
rs573708524 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398272 | AGAAAGGCCCATGCT[A/G]CCAATTCTTCATAGT | 10213 |
rs573712508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341044 | CCGCGGGATCCCCTG[C/G]CCCTTCGGGCTCCCC | 10213 |
rs573730760 | in-del | -/TTGA | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161372689 | GAGGTTGAAAAATCC[-/TTGA]TTGTTATTAGCTTTA | 10213 |
rs573747405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161333636 | AGGATCTTGTTCCTA[C/T]TCTTCTTCCAGAGTA | 10213 |
rs573757934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161346535 | TTTGTATGTCTGATA[C/G]TTTTTACTAGATGTT | 10213 |
rs573810371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161374392 | TGACTTTTGTGACAT[C/T]CCTAGGAGTAAACAT | 10213 |
rs573838291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391912 | CCTAGTGCTTTTAGA[A/T]AACATACCATGTTTA | 10213 |
rs573901589 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161392460 | CTCTCCACGCTTACC[C/G]CCTCTTTCAACCAGA | 10213 |
rs573934517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339307 | TGCCAGTACTTGATA[C/T]GGTTAATTTTTTTAA | 10213 |
rs574096041 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382378 | ATGAACAAAATTTAT[C/T]CAACAAGAAAACAGA | 10213 |
rs574106230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344757 | GTTATTTTTCTTTTT[A/G]TCATTGAGTCATAAG | 10213 |
rs574147671 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379051 | GTCCTTTATTCTCAT[A/C]CACATGCTCTACTGC | 10213 |
rs574161081 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406397 | TAAACCGAAGAGCAC[A/G/T]AATGCAAAAGCAAAA | 10213 |
rs574166862 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394542 | CTTATAAATTTCATT[A/C]ATTCATTCATTCATC | 10213 |
rs574182143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357202 | GCCTCAGTTAATTTA[A/G]CCACATTTAAAATTT | 10213 |
rs574207767 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353089 | TAAAGAGAAAATAAT[A/C]TGGCTTTAAGACTAT | 10213 |
rs574254416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161364735 | TCTCTGGCAGTATTT[A/C]ACTGGTACCAACCTT | 10213 |
rs574347628 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352849 | GGAAGGTTATTTGTA[A/T]TCTGTGTTAACACCT | 10213 |
rs574356633 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353693 | TTTTGTACTTATTCT[A/G]TATTGCAGTTATGGT | 10213 |
rs574394382 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357915 | GTTCTTTTTTTTTTT[A/T]AATGGTGGTGAAACA | 10213 |
rs574398259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161402824 | TGGTTACAAACACAT[A/T]AAAAAGATGTTCAAT | 10213 |
rs574460100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371874 | ATTCTGAAAACAGAT[C/T]AACTTGCAAAGCATA | 10213 |
rs574469617 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390031 | CACTGAGCCCGACCC[G/T]GCATTTTATTTTCAT | 10213 |
rs574521934 | in-del | -/CTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344639 | ATTTCTGGTGTTCTT[-/CTT]TTTATTGTATAGATC | 10213 |
rs574549694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360131 | ATGGAATGATTTAAG[C/T]TTCAGGTTAAACAAA | 10213 |
rs574566511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161399327 | CATAAAATAACAACT[A/G]ACATTTACTGAGTGT | 10213 |
rs574577786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320355 | GTTTTACTGACCACA[A/G]ATTGAGCTACATTAT | 10213 |
rs574604940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409361 | CACTTTTCTAAGAAG[A/G]AATATATATTTTAGT | 10213 |
rs574605799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400172 | AGAAAGGTATGTCTC[A/G]TATTTCAAGTCCAAT | 10213 |
rs574646528 | in-del | -/AG | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161355351 | GTTTTTACTAAAGTC[-/AG]TACTTTCAGGATTAC | 10213 |
rs574677755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161352209 | CAGTGATTTTCAACC[G/T]TGGCTGTACTTTAGA | 10213 |
rs574678957 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161337454 | TGGTATGATTAGCAC[C/T]ATTCACAAGGGAAAA | 10213 |
rs574710793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360827 | AGGCGTGAGCCACCA[C/T]GCCTGGCCTTCGTAT | 10213 |
rs574792653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407043 | CCAAAATTTTTGCCT[C/G]CTTCCAATACTGTAG | 10213 |
rs574820907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370472 | CTGTCTAGTCACTTA[C/T]AATTGAAAGAGCTTG | 10213 |
rs574848685 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306918 | TAAAAGGAATCAGAC[C/T]GAAGGCGGAAAGATC | 10213 |
rs574872432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336889 | CTATGTGTTATTTTT[A/G]TATTCTTAATACACT | 10213 |
rs574887958 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314533 | TATCTTAGCAATTTA[A/G]CACTTTCTCCATTTT | 10213 |
rs574890275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379580 | AGGGTAACTTTTTTC[C/T]AATTTTAACACTCTT | 10213 |
rs574903478 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331759 | TTAAAATTTTCCTCT[A/G]GAATTTAAAAAAAAT | 10213 |
rs574910799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161321893 | GCCAGGGAACTCCAC[C/T]TGGTGTAGCTTTGGT | 10213 |
rs574918015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354995 | GAAAAGAAACTTTTC[A/G]GAGAGGCAGGAACCG | 10213 |
rs574921634 | snp | A/C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161381599 | CAAATTTAGTCTAGT[A/C/T]TTTCAGTGACCTAGC | 10213 |
rs574933877 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161390771 | ATGAGCCCCCTAGAT[A/G]TCATAAAGTTAGATT | 10213 |
rs575001178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331021 | TTTGAAAAGTTCACC[A/G]TTCTGTTTTATAGAA | 10213 |
rs575010966 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161397677 | TATAAAATTTACCAA[A/G]TGTAGCAATAAGACT | 10213 |
rs575013983 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307726 | CCTAGACCTAGAGTG[C/T]AATATCAACTTGTCA | 10213 |
rs575068277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380541 | TTTCTCCCAATATAC[G/T]GAAGTTGTACTACAG | 10213 |
rs575116127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322950 | CTTGTTCTTGGATCT[C/G]GTTCTCTTGACACAC | 10213 |
rs575117120 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | PSMD14 | GRCh38.p7 | 2:161405042 | ACTTCAGATGCTGCT[C/G]TTCAAGAGTAAGCAA | 10213 |
rs575158863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161345864 | TGTGTTTCATTTTTC[G/T]GTTGCTACATCTTCA | 10213 |
rs575161978 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403831 | CACTTTTGAGACCCT[C/T]ACCATACCACCAAAT | 10213 |
rs575200773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161363628 | TTTGCCAAAAGATAA[C/T]GTATGTAGATGGTCC | 10213 |
rs575237034 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161356145 | TTGAAAGGGTTAAGT[C/G/T]GACATGAAAGAATTC | 10213 |
rs575260340 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406514 | TGCAATCATTTCTTA[-/C]GTTTTTCCTGGTAAC | 10213 |
rs575359149 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348737 | GGTGACATCTGAGGA[C/T]ATGGAGTAAGGATGC | 10213 |
rs575422811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161331593 | CAGCCATTCTATAAG[C/G]CTTTTGCCTTGGGAG | 10213 |
rs575435683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391640 | TCTGTCTCCCAGACT[A/G]GAGTGCAATGGTGTG | 10213 |
rs575489529 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391787 | GGTGGGAGGTAGAAA[C/T]GGAGTCTTGCTTTGT | 10213 |
rs575491981 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161344863 | TCACTTTCTTGAGGG[C/G]GACCTTTGAAAAGGT | 10213 |
rs575494895 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357970 | CTTGAATAGTTCACA[-/T]TACTGTATAAGCTGA | 10213 |
rs575496890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408450 | ATGGGAAATTGGGAA[A/G]GAACTGTGCAAATAG | 10213 |
rs575507221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340887 | TGGTTTCCCCTCAGC[C/T]TCCCGGGGCTGTATT | 10213 |
rs575514437 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161353044 | TTTATAATTTTATTA[A/T]AAGAATATTTTGTTC | 10213 |
rs575520470 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348069 | AAATGTACCATAAAC[A/T]TGTATATGCTAGTGA | 10213 |
rs575560106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161362911 | ATTTTCTTCAGCTTT[C/G]CCTTTGTTTATTGTT | 10213 |
rs575575980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161409607 | ATCTCACAAGCTATG[C/T]AGGTTTGGGCCAGGA | 10213 |
rs575594993 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSMD14 | GRCh38.p7 | 2:161358705 | ATCCCAACACTTTGG[A/G]AGGCTGAGGCGGGTG | 10213 |
rs575637926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161359265 | GTGTGAGCCACTGTG[C/T]CTGGCCCTACTCAGT | 10213 |
rs575648916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161354051 | AGGGCCACTGGCACT[A/G]TAAGAACTCTAAAGC | 10213 |
rs575656854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161410750 | TTCTTCAACTACAAA[C/T]GGCAGCTTTTGATCC | 10213 |
rs575710835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371027 | TAATATGGTGTACAA[C/T]TTCAGGGTTTCTAAT | 10213 |
rs575719320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314655 | TGAGCTTTTGTGCCT[A/G]GCTTCTTTTACATAG | 10213 |
rs575737701 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311149 | CTACTAAAAATACAA[A/G]AATACAAAAATTAGC | 10213 |
rs575744221 | snp | A/G | 0 | 0 | intron-variant | PSMD14 | GRCh38.p7 | 2:161381928 | ATTAGTAAAGCAACC[A/G]TGGTACTGAAATCTG | 10213 |
rs575821129 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334052 | ACAAAAAACAAAAAG[A/G]CCAGGCCTGGTGGCT | 10213 |
rs575883954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371993 | TTATTTCTTTCTTTC[G/T]AGCCCCATATGCCAT | 10213 |
rs575892405 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307866 | ACCCTGTAAACTAAA[C/T]TCGGCTTAAAATAGG | 10213 |
rs575904538 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326463 | TTGATGGTAGAAATG[C/T]AAAATGGTACAGATA | 10213 |
rs575928173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161315313 | CTGAAGTTAGTAAAT[C/T]CTGGCTAATTTTATT | 10213 |
rs575930077 | snp | A/G | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307960 | CAAGAGGTGGATAAA[A/G]CGGACTTACAGAAAA | 10213 |
rs576036564 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323315 | CCTGTTTCTCATTAC[A/G]GTGTCCATTCCTACA | 10213 |
rs576109838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161387253 | ACCTTAATACACTTT[C/G]TTATTTTTCTAAGAC | 10213 |
rs576139668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161375584 | GAATGTAGAAACAAT[A/G]TCATTCCAAGTGGTA | 10213 |
rs576176358 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357166 | TAATCTTCTAAATGG[-/A]AAAAAAAAAATCCAC | 10213 |
rs576261119 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373483 | GTGTCAAGTCCTCTC[A/G]TCTCTATGAATCAGA | 10213 |
rs576278701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161396910 | TCAGCTCACTGCAAC[A/G]TCTGTCTCCTGTGTT | 10213 |
rs576295559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318610 | ACTGGGGATAACCCA[A/C]AACCAAAGCAGTAAA | 10213 |
rs576422165 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PSMD14 | GRCh38.p7 | 2:161323293 | AGTTTTTATCATGCT[C/G]TCTTTTCCTGTTTCT | 10213 |
rs576437638 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398945 | CAATCAAACATAAAA[A/G]TCTAAGAGAATAAAC | 10213 |
rs576480980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313469 | GTCCTCCTACCTCAG[C/T]CTCCCCAGTAGCTGG | 10213 |
rs576494339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329369 | GCTTTAATTTTTGCT[A/G]TAAGCACTGGCATAG | 10213 |
rs576505727 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161369603 | TAAAGACAGTACTCT[A/C]TCGCCAGAGAGATGA | 10213 |
rs576537033 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343060 | ATAGTTGTCTTTTTT[A/T]AATTGTGATCATACA | 10213 |
rs576573659 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342131 | TTAAATCCTGATGGC[C/T]CTTTATTTCTTGCCT | 10213 |
rs576590468 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343720 | GTAATTTTAGCTCCT[C/T]GGGAGCCTAAGGCTG | 10213 |
rs576601925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161368766 | GCTGTTAGTTCTATT[C/T]GAAGTTCTGTAAGTT | 10213 |
rs576620482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327901 | AAACAAACCTGTGGA[A/G]TTAAGTGTTAATGAA | 10213 |
rs576625347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161406643 | TGATTTGGAATATCT[G/T]AGAATTGAAGAGATA | 10213 |
rs576647985 | in-del | -/ATTA | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161394539 | ATACTTATAAATTTC[-/ATTA]ATTCATTCATTCATC | 10213 |
rs576711443 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161322765 | TCACAGTTGATACTG[-/AT]ATTTCATTGTTTTTG | 10213 |
rs576725035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334856 | AGGCATGAGCCATCA[C/T]GCCTGCCGTTTGATG | 10213 |
rs576746099 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161360088 | GCCTGAAAAATTCCA[C/G]ATTTTCTCTGATAGG | 10213 |
rs576762256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161328225 | GTTGAAGAATATTGT[G/T]AAAGCATTGTTTGTA | 10213 |
rs576779137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343218 | CATTAGACCATAATA[C/T]TTCATCTTCCACCCC | 10213 |
rs576785832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161380343 | TAACTTAAGTAAATT[C/G]TTTTCCCAGTGTTTC | 10213 |
rs576806955 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313641 | AGGCATGAGCCACCA[C/T]GCCCAGCCTAAATAC | 10213 |
rs576827253 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PSMD14 | GRCh38.p7 | 2:161328007 | GGTTAGGAATTATAG[C/T]TCAGTGCTTAGATCT | 10213 |
rs576852233 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382789 | TATAAGATATAAACT[A/G]AACTAATTTAATGTC | 10213 |
rs576876703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161407544 | TTAGACACTTGCCAT[C/G]TTTGCTCATTTTCAA | 10213 |
rs576912166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161343801 | CCACTGCACTCCAGC[C/G]TAGGGGATGGAGTGA | 10213 |
rs576923023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161377215 | GGGTAGTCCTAATCA[G/T]AAATTATACACACCT | 10213 |
rs576931099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161366737 | TTGAGGGTAAGAACT[A/G]TATGTCAGTTACCTT | 10213 |
rs576939355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161311280 | CGACACTACACTCCA[A/G]CCTGGGCAACAGAGC | 10213 |
rs577012373 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161349517 | CTAGTGTGGAGTTCT[C/T]TCAATTATTTCAGTA | 10213 |
rs577068669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389312 | TTCCAGCTCAAGCTC[A/C]ACTCTCTACGCCAGA | 10213 |
rs577094366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161312145 | TCAGTCTGAAAAGTA[A/C]TTTTTTTTTTTTTTT | 10213 |
rs577100757 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PSMD14 | GRCh38.p7 | 2:161389930 | AGATGGGGTATTGCT[A/T]TGTTGTCCAGGCTGG | 10213 |
rs577106765 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161378666 | GTCAGGACAGCTATT[A/T]TAACAAACAGCTTTA | 10213 |
rs577131227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161313537 | GTATTTTTAGTAGAG[A/G]CAGGGTTTTGCCATG | 10213 |
rs577140492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161379434 | ATAACCTTCAGTACA[A/G]CTATACACTTTCTTA | 10213 |
rs577175429 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PSMD14 | GRCh38.p7 | 2:161320685 | GAAACGTTAAGTGTA[-/T]TTTTTTTGCCTAATA | 10213 |
rs577261652 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PSMD14 | GRCh38.p7 | 2:161361111 | ATTCACCAATATTTT[C/T]GGCATAGCATTTGTT | 10213 |
rs577266824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370326 | ATCAGTGCCATGCAC[C/T]ACCTGTCTAGTATAT | 10213 |
rs577310378 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372307 | GTACTTAGAAATAAA[C/T]ATTAGCTTGTTATCT | 10213 |
rs577388919 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161336679 | CTCCTAGGTTCAAGT[A/G]ATTCTCCTGCCTCAG | 10213 |
rs577419574 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332018 | GGTAGATAAAATGAA[G/T]AGAGTTGTCATGGCT | 10213 |
rs577427916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161400908 | AAATATAGGAGACAC[C/T]AGTCTGTTTTATCAT | 10213 |
rs577446381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161314267 | TCTTTAGAAAACAGG[C/T]TATTGCAAAATTTTG | 10213 |
rs577480102 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335818 | TTGAATTTAGGCTTT[A/G]CTACTTAGTCACTTT | 10213 |
rs577501014 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161383555 | AGAAATAATATAGAC[G/T]TCTACAAGTAAAATA | 10213 |
rs577522479 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332173 | GACATGTAATACTTG[A/G]CCCATGTTTTAAGAC | 10213 |
rs577532803 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161386393 | AACCTTGCTCTGTCA[-/T]TGAGGTTGTCTTTGG | 10213 |
rs577532852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161329548 | TTTATACATTTATGA[A/T]GGTCCTTTCTAAACA | 10213 |
rs577537241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161316809 | TATGTTTCCTCTTTG[C/G]TGTGATATCTAATTT | 10213 |
rs577540337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161384617 | GAGTTAAATTCCCTT[A/G]AAGTGGCAATCTGTC | 10213 |
rs577660905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161310120 | CGCGCAACTGCACTC[A/C]AGCTTGGGCAACAGA | 10213 |
rs577671691 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PSMD14 | GRCh38.p7 | 2:161327019 | TGATTGTACATACAA[A/T]GGAATATTATTAAAC | 10213 |
rs577699559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161317582 | TTCCATGGCCATATC[A/G]TTTGTTTTCTTTTCT | 10213 |
rs577699809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161365332 | GCTTGCAGTAGTACC[G/T]TAATTTATTCATTCA | 10213 |
rs577700525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161309438 | ATAGAGTTATAGTGT[C/G]AAAGTGATTTTGTTC | 10213 |
rs577703577 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161325601 | TCTTTCCAATTAATC[A/C]TACATTCAACCCAGT | 10213 |
rs577746140 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSMD14 | GRCh38.p7 | 2:161339472 | GTTGCCTGGTTTTTA[C/T]TGGGTGGGTTATTTT | 10213 |
rs577780816 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSMD14 | GRCh38.p7 | 2:161340117 | CTGCTATAGCAGAGT[A/G]GAGATTTGGCTGAGC | 10213 |
rs577885267 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311984 | TAATTAAATTTAATG[C/T]TGACTCACTCACGAT | 10213 |
rs577904674 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161319754 | TAATCTGTGTTTACT[A/G]TAAGAAGCAGTTTTT | 10213 |
rs577931083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161332555 | TCTGTGAAATTGTTG[A/G]TCAGATGGGTTAGCT | 10213 |
rs577973293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334130 | CTGAGGTTGGGGGTT[C/T]GAGACCAGCTTGACC | 10213 |
rs578012642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161334678 | GAAGAATAGAATTTT[C/T]CCTTCTTTGACCACT | 10213 |
rs578100116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395906 | CCATAACACCTTCAT[A/G]TTCAGATTGTCCACA | 10213 |
rs578196442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161357970 | ACTTGAATAGTTCAC[A/T]TACTGTATAAGCTGA | 10213 |
rs578228080 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PSMD14 | GRCh38.p7 | 2:161341104 | GCCCCGCGGGCTCTC[C/G]AGGCTCCTCCGGCCC | 10213 |
rs745307744 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349082 | CCCTTTTGCTCAGTC[C/T]GCTGCCGAATTGGCT | 10213 |
rs745352869 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391648 | CCAGACTAGAGTGCA[A/G]TGGTGTGATCATGGC | 10213 |
rs745409795 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333543 | GGAGTTAGGCCAGAT[C/T]TAGACACTAGCTGAG | 10213 |
rs745426967 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332974 | TTTCAAATATCTCAC[C/T]CCCTTAAATAAGTGT | 10213 |
rs745442741 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392599 | AGTTTTAAAAGGTCA[A/C]ATCCACTCATAAACT | 10213 |
rs745455038 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360838 | ACCACGCCTGGCCTT[C/T]GTATTTATTTCATCA | 10213 |
rs745516140 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357724 | CTTATTTACTTTTCT[A/G]TTGTCAGTGATGTGT | 10213 |
rs745592568 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313301 | ACTGTATTAGAAATG[-/T]TAGTAAAGCTTAAAC | 10213 |
rs745639974 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161381568 | TAAAAATTGGGAACT[A/G]TAGATTGGTGCTTTA | 10213 |
rs745686746 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324586 | TACTTGGTGATTTTT[A/G]CTTTTTTCCCCTAGG | 10213 |
rs745691778 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161350095 | TAAAGAAATGTTGGT[A/G]TGTTTAGTAATATAA | 10213 |
rs745746948 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403543 | AAATGTACCTCATTT[A/T]TAAAAATGCAAATTG | 10213 |
rs745747841 | snp | C/G | 2.22319e-05 | 0.00333398 | missense | PSMD14 | GRCh38.p7 | 2:161408837 | GTGTTTCATTCACAG[C/G]CTGTAGAAGAAGAAG | 10213 |
rs745772005 | in-del | -/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161407548 | ACACTTGCCATCTTT[-/G]CTCATTTTCAAGTTC | 10213 |
rs745837788 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347516 | CTCAGACGTTAGATC[A/G]TATTAAGATAGTGCT | 10213 |
rs745896083 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161367337 | AAATGTGTTTTGATT[A/G]TGTCATAGCCAAATA | 10213 |
rs745896314 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312352 | TTTTGCCATGTTGGC[C/T]AGGCTGGTCTTGAAC | 10213 |
rs745953777 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323333 | GTCCATTCCTACAAA[A/G]CAACTAAGTTTTATT | 10213 |
rs745996492 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161351783 | CTCAAGCTGATACAG[C/T]GCTATCATTGAACAC | 10213 |
rs746017629 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161369340 | AAGACATATGTCTCT[A/G]TTGCATATTCTTCTT | 10213 |
rs746028220 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161407316 | TAATAGAGTGACATC[C/T]GACTCTGAAAATGAG | 10213 |
rs746070897 | in-del | -/TTAT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383916 | AACAATTGTTTGAAG[-/TTAT]TTATGATAACATCTG | 10213 |
rs746084553 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335307 | TGTCCAGTGGAACTT[C/T]CTGTGGGTTGGAAAT | 10213 |
rs746122868 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161408569 | CAGTAACAGTTTGCA[A/G]ATGGTCAACACAATC | 10213 |
rs746123067 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394226 | ATTCACCCTCCTTGG[C/T]CTCCCAAAGTGCTGG | 10213 |
rs746217161 | snp | A/G | 1.86981e-05 | 0.00305756 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161411391 | GTTGGATACTGTCGT[A/G]TTTAAATAAAGCAAC | 10213 |
rs746247289 | in-del | -/TTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339497 | TATTTTGTTAATGAA[-/TTT]TTTTTTTTTTTTTTT | 10213 |
rs746322029 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337142 | ATGAGCAAGAGGGAA[A/T]CGTGCTTTGTTTTGT | 10213 |
rs746345582 | in-del | -/AGA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161410850 | GCTATTATAAAACAT[-/AGA]AGAAGTGCTGAGAAT | 10213 |
rs746352372 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344961 | CTAAGAAATGCTTGT[C/T]TAACCCAAGTTCATG | 10213 |
rs746364063 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386306 | ATTAATTAAAAGGAC[A/G]GAAATACCATGTTTG | 10213 |
rs746422626 | snp | A/G | 2.54839e-05 | 0.00356949 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371331 | AGGAAAGGTAGAGTA[A/G]ATTCTATCTTTATTG | 10213 |
rs746453493 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346525 | TTTTTGCTGCTTTGT[A/G]TGTCTGATAGTTTTT | 10213 |
rs746459252 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363178 | GGTTGCATGCTCCAT[C/T]TATAATGCCTGATGA | 10213 |
rs746466545 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403246 | GATACATGCTACTAC[A/G]TGGATGGACCTCTAA | 10213 |
rs746502642 | in-del | -/GTTTA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371927 | ACCCCTTTTGTTCTT[-/GTTTA]GTTTAGTTCTCTTTC | 10213 |
rs746508470 | snp | C/T | 4.2084e-05 | 0.00458696 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391068 | ATTAGGTGAAAAATA[C/T]TAATTTGTCCTTTTT | 10213 |
rs746554313 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389460 | GATCTGTACAGTATA[G/T]CATTTTTATGCACTA | 10213 |
rs746594353 | snp | A/G | 2.64016e-05 | 0.00363319 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371337 | GGTAGAGTAGATTCT[A/G]TCTTTATTGCCATCT | 10213 |
rs746663160 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372323 | ATTAGCTTGTTATCT[A/G]TCAGACCTGGAGTTT | 10213 |
rs746677737 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391333 | GCACAAAATAAGGGA[A/C]TATTTTATTGGACTA | 10213 |
rs746686372 | snp | A/T | 6.00619e-05 | 0.00547972 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370205 | AATGATCAGTTAAAG[A/T]AATAATGGGAAATAT | 10213 |
rs746711548 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336610 | AGACGGAATCTTGCT[C/G]TGTTGCCCAGACTGG | 10213 |
rs746754454 | snp | A/C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377964 | CCAGCAAGTGGAAAC[A/C/G]TGGAAACTATGACTT | 10213 |
rs746777259 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395623 | ATTTTATGAACGTTT[C/T]CATTATTTAATAATT | 10213 |
rs746788316 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378804 | TTCCTCATCCATAAA[C/T]TGATAATATTAATAC | 10213 |
rs746834380 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321504 | TTTCACTCCCAATTG[A/T]CACAAACCTGGCGGT | 10213 |
rs746910267 | snp | C/G | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307439 | AAATGAATAGAGAGG[C/G]ATAGGTTTGGGGGGG | 10213 |
rs746931069 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322573 | TTTTTTATTTTTAGT[A/G]GAGGTGGGGTTTCAC | 10213 |
rs746984938 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401965 | TTATCTCTAAAATGA[A/G]GTTAAGGATTGTGAT | 10213 |
rs746985526 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343273 | ACTTTCTGTTTGTTA[-/C]GAATCTCACTATTCA | 10213 |
rs747015543 | snp | A/G | 1.71968e-05 | 0.00293225 | missense | PSMD14 | GRCh38.p7 | 2:161411309 | TCTTTTAGGACCCCA[A/G]ACGTCATTTGGAGGA | 10213 |
rs747024281 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161325271 | TTCCTGAATGTGGTG[A/C]GATATAGTGTACATT | 10213 |
rs747073963 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161316791 | AAGTTTTAATTTGTT[A/G]AATATGTTTCCTCTT | 10213 |
rs747076701 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343512 | ATTGTGAATATTGCT[A/G]CTATGAACATTGGTG | 10213 |
rs747125978 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401087 | TGCCATTTCAGACAG[A/G]CAATTCACCTTGTAA | 10213 |
rs747127129 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161319458 | TGTTGGGCAAATGAC[C/T]TCTAGATTTCTGCCT | 10213 |
rs747128037 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326384 | GCTATTATCCAAATT[A/G]AACAACAACAACAAC | 10213 |
rs747206139 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161367096 | CCATAGCCTTAATCT[A/G]TTAATACTCAAAGAA | 10213 |
rs747261736 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405970 | ATGTTGGAGTAGCTC[A/T]AAGTATGTTCAGAAA | 10213 |
rs747297170 | in-del | -/AT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376107 | TATGTATATATATAC[-/AT]ATATATATATATACT | 10213 |
rs747304003 | snp | A/G/T | 3.61979e-05 | 0.00425416 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318904 | CTTGAGCATTTCCTT[A/G/T]TGTGTAAACTACAAG | 10213 |
rs747328901 | snp | G/T | 1.94664e-05 | 0.00311975 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318782 | ATTGAATAAACATTT[G/T]TGTGCTTAGGAACGT | 10213 |
rs747352565 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368212 | CAGAGTGTTAGTTTG[A/T]TTTTGAACCAAGTGT | 10213 |
rs747354450 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161334610 | GCTCCTCTGTAGAGC[A/T]TTAAAGGAAGTATAA | 10213 |
rs747356948 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317082 | ATTTTTTTCTTCTTT[C/G]GTAATATATTCTAGA | 10213 |
rs747386957 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318277 | AGTATAATGAGTTCA[G/T]TTTTTAAAAGCCTTT | 10213 |
rs747561987 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378974 | TTGAGAGACAGTAGT[C/T]CAGTGGATATACTTT | 10213 |
rs747608240 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359782 | ACTAAGCTCCCAGAA[A/T]AAAAGTAGACTTGGG | 10213 |
rs747609023 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310123 | GCAACTGCACTCCAG[C/T]TTGGGCAACAGAGTG | 10213 |
rs747615586 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321204 | CAGAATTCCCTCCCA[A/G]ATAGGAGCAGGTCAC | 10213 |
rs747635676 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354458 | TCATGTTGCCCAGGC[C/T]GCTGAATGATGTTTT | 10213 |
rs747683730 | in-del | -/ATAAG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161409196 | TTTACCTACAGATAA[-/ATAAG]ATAATAGAAGGGTAG | 10213 |
rs747695641 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360869 | TGTATTTCTGATGTA[A/G]TTAGTCTCTATTATT | 10213 |
rs747779395 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346490 | TTGACTGACTTATCT[C/T]CTTACTGTGGGCCAT | 10213 |
rs747781050 | snp | A/G | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307734 | TAGAGTGTAATATCA[A/G]CTTGTCAAGTATATC | 10213 |
rs747855617 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161351721 | TCATACTGTATGTCT[A/G]CATGGGTCGTCTGGG | 10213 |
rs747887993 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313002 | TATTATATGCTTACT[A/G]TATGATAAGCATTGT | 10213 |
rs747917516 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406974 | TTGTTTGCAATATTC[C/T]GCAATACTCCCTAAT | 10213 |
rs747941267 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161407308 | ACTGAAAATAATAGA[A/G]TGACATCTGACTCTG | 10213 |
rs747972748 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324838 | TTATATTTTTCTGTC[A/G]TCTTTGAAGTTAGCC | 10213 |
rs747996352 | in-del | -/AGTCCTCTCATCTCTATGAATC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373474 | GTTCTTTCAGTGTCA[-/AGTCCTCTCATCTCTATGAATC]AGATTAAATGCTAGT | 10213 |
rs748031035 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394172 | CGACAGGCTTTCACC[A/C]TTTTAACCAGGCTGG | 10213 |
rs748111519 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337777 | GCTGTAGCAGGAAGG[A/G]GATTAGACTATGGAT | 10213 |
rs748171062 | snp | A/C | 2.05827e-05 | 0.00320795 | missense | PSMD14 | GRCh38.p7 | 2:161408865 | AAGATAAGATGACAC[A/C]TGAACAGCTGGCAAT | 10213 |
rs748231530 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396963 | CTCCCAAGTAGCTGG[G/T]ATTACAGGCGCCCGC | 10213 |
rs748272236 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346048 | ACCACTCTCAGCTAA[-/T]TTTTTTGTATTTTTA | 10213 |
rs748286860 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322899 | AATTTTCTCTAAATA[A/G]GAGGTGACTTTTCTC | 10213 |
rs748288991 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398565 | TTTTGATAATGTTTG[A/G]TTACATATTTGTAAA | 10213 |
rs748326191 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383635 | GAATTTTGTTGTGAT[A/G]TATAATGAAATTTTC | 10213 |
rs748339998 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324862 | GTTAGCCTTGCCATG[A/G]TTTTGCTTTGACCAA | 10213 |
rs748386128 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363430 | ACCCTTGTTTCTCCT[A/G]GTGTGATTTTAATTC | 10213 |
rs748438794 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161361525 | AATTGGGAAACTTGT[A/T]AATTTTTCAGTTTGT | 10213 |
rs748461555 | in-del | -/AA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343829 | TGATACTCTGTCTCA[-/AA]AAAAAAAAAAAATGT | 10213 |
rs748479733 | in-del | -/CTA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161370742 | ACTGAGTTCCTAGTT[-/CTA]CTGCTGGTTTAATTG | 10213 |
rs748502700 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161369982 | ATAATTGAATGACTT[C/G]AGTAGGTATCAAATG | 10213 |
rs748505377 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161329771 | AATCATTCTATTCAT[A/G]TACTCTGATATTTAT | 10213 |
rs748512807 | snp | A/T | 2.01225e-05 | 0.00317189 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367748 | CAGAGACCTCAACGA[A/T]ATTTGCTTTGTGTCC | 10213 |
rs748588584 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372091 | ATGTGAGAGGCAATT[C/T]GATTTTGCTCAACCA | 10213 |
rs748596420 | snp | C/G | 1.85129e-05 | 0.00304238 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318916 | CTTGTGTGTAAACTA[C/G]AAGCCTTTTTGTAGT | 10213 |
rs748597300 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161308763 | TCTCTTCGCCTGCTC[-/T]TCAGGGCTCTCTGGC | 10213 |
rs748616445 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354679 | AGTGGGTATATATAT[G/T]TATGAAGTATACACA | 10213 |
rs748679496 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161410586 | ATACAATTTTAAGCC[G/T]CCTTTTTAACTCAGT | 10213 |
rs748719236 | in-del | -/TG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161319515 | AGAATTTGTGCCTCT[-/TG]TGTGAGTTCGACACT | 10213 |
rs748767621 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389565 | AGTCACTGCTCCCTA[G/T]GGAATTTCATAGCTC | 10213 |
rs748775260 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375687 | GTTTAAACAACTAGC[A/G]TTTTACAAAAGATGG | 10213 |
rs748794194 | in-del | -/C | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307413 | GGCTACTCACCCCCT[-/C]CTCCCATAAAAAATG | 10213 |
rs748865435 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377252 | TTTGTCTAGTTTTCC[A/C]GGTGGAAAGAGAAAA | 10213 |
rs748919950 | in-del | -/T | 1.68084e-05 | 0.00289895 | frameshift-variant | PSMD14 | GRCh38.p7 | 2:161367855 | AGAATTTGTTGATGA[-/T]TATACCGTCAGAGTG | 10213 |
rs748972854 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400464 | ATAGGGCCACTTATA[C/T]ATGGATTTTTCTCAT | 10213 |
rs749037331 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310291 | ATATTATTGCTGTTG[C/T]TATTGTTATTATCTT | 10213 |
rs749044116 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365069 | CAAGATCGCGCCATT[A/G]CACTCCAGCCTGGGT | 10213 |
rs749087180 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311452 | AATGATTTTAAAGTA[C/T]ATAGGAGGATGTGCA | 10213 |
rs749104801 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404458 | ATTTAAGGAAATGCA[A/G]TGTCCTCTAAGGGGC | 10213 |
rs749116799 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405146 | TCTAGGCATCGTGTA[A/G]GTTTGAAACTTTGGA | 10213 |
rs749166746 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391989 | TTCAGATAATTTGTA[C/G]TAGATTCTGATCCCA | 10213 |
rs749175543 | snp | C/T | 8.95857e-05 | 0.00669215 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161391154 | CATTACTATTAACTA[C/T]CGGAAAAATGAACTG | 10213 |
rs749224487 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161351523 | TCTCTGTAAAGGAAA[A/G]CCCTTTGCCCCCATT | 10213 |
rs749258740 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392645 | GTGCTTGAGCATGTG[A/G]TGAGTGAGGGGAGTG | 10213 |
rs749334888 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314740 | ATTCCTTTTTATAGC[C/T]GAACAGTATTTCATA | 10213 |
rs749353822 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373040 | TGTAAATAAATGAGT[A/T]TGTATTTTATTTTTG | 10213 |
rs749383395 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161408714 | ATTTTATTTGTTCAG[C/T]AAATTATTTGAATAA | 10213 |
rs749404195 | in-del | -/TAGCATAGGTAGTTG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393264 | TTATAGGTAGCTGTA[-/TAGCATAGGTAGTTG]TAGCAGCACCCACAT | 10213 |
rs749436085 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336666 | CTGCAACCTCTGCCT[C/G]CTAGGTTCAAGTGAT | 10213 |
rs749504533 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396882 | ACCCAGACTCAAGTG[C/T]AGTGGGGTGATCTCA | 10213 |
rs749536471 | snp | A/G | 2.25864e-05 | 0.00336046 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408909 | AAGCAGGTGAGGTGT[A/G]CTGTTAATAAGTTAT | 10213 |
rs749609020 | in-del | -/GTAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313142 | AAGGACAGGGAACTT[-/GTAA]GTGTCAGAGCCAGTA | 10213 |
rs749634190 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358404 | AATCTTTAGTTTCTT[A/G]TTTATGTCTAGGATT | 10213 |
rs749681133 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397825 | CATTAGTGCTAGATT[G/T]TAGGGAAAATATTTC | 10213 |
rs749719232 | snp | G/T | 7.0814e-05 | 0.00594996 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370096 | ATAATTTTTCTTTCT[G/T]TCTAAATCAGGGTGT | 10213 |
rs749744378 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310785 | GTAGGTGGTGACGCC[A/G]GATTCAAATTGAGGT | 10213 |
rs749782476 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161407414 | CATTTCCTAATGATG[G/T]GTTGTAAATAAGTAT | 10213 |
rs749792486 | in-del | -/ATAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365722 | GGGGGTGATGTTTTG[-/ATAA]ATATATATGTTATGG | 10213 |
rs749860178 | snp | G/T | 1.96632e-05 | 0.00313547 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367760 | CGAAATTTGCTTTGT[G/T]TCCACATCTCTTCCT | 10213 |
rs749883798 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363410 | AAATTTGTTATAATA[C/T]TTTTACCCTTGTTTC | 10213 |
rs749905617 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405203 | TCCAGCCATTCTCCC[A/G]TGGTTTTTCCCTTTC | 10213 |
rs749915022 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365977 | ATCACAACCAATTTA[C/T]TGTTGTCCTCACCTT | 10213 |
rs749934160 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403085 | ATTCAAACAAAAAGC[A/G]TGTATATGAATGTTC | 10213 |
rs749946203 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382996 | CTGTAAATACACAAA[C/T]ATGGAGAAACGCTTT | 10213 |
rs749973925 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400067 | CTATACTTTATGTAA[C/T]GCCTGAATTATTTTC | 10213 |
rs749983239 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312643 | AAACACTTTATTCAT[A/G]TTGTCTGATAATATT | 10213 |
rs749995650 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406561 | GTGAATGAAGACAAA[C/T]TGGTCTTGCCCAGAT | 10213 |
rs749999408 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161351167 | GTGACTCAAGGGGAT[A/G]GGAAAGAGAAGTCCA | 10213 |
rs750039377 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352336 | TAAGCTCTCCTTGTA[A/G]TTCTGAGCTATAAAT | 10213 |
rs750178161 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339276 | GTGTGTGAGAGTTCC[C/T]GTTCTTCCACATCCT | 10213 |
rs750233345 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343179 | TCAGAACTTTTTCAT[C/T]GTCCCAAACTGAAAC | 10213 |
rs750247533 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391850 | GTGATCCTCTCACCT[C/T]AGCCTTCTAAAGTGC | 10213 |
rs750255187 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161399703 | TCAAAAAAAGTTAAA[A/G]TAAATAGAAAAATAT | 10213 |
rs750324786 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326157 | ATTCTTCTGCCTCAG[C/T]CTCCTGAGTATCACA | 10213 |
rs750387361 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338188 | GTTTTTTCTTTTTTG[C/T]CTAGAATTTCTCTCC | 10213 |
rs750401366 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161364694 | ATCTGTCCCATTGAT[C/G]GTGTATTATATGCGA | 10213 |
rs750409298 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326691 | GATAAATAAAATGCA[A/T]ATACACTCATTCCTT | 10213 |
rs750449543 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402518 | TGGTGGCATGCACCC[A/G]TGGTCCCAGCTACTC | 10213 |
rs750489415 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346162 | TGCTGGGATTATAGG[C/T]GTGAGCCACCGTGCT | 10213 |
rs750496791 | in-del | -/TTTC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161355536 | CATTTCCATTCTTAT[-/TTTC]TTTCTTTCTTTCTTT | 10213 |
rs750536712 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388982 | AAGTGAAATTGAAAG[A/G]CTACTTGAGGATATC | 10213 |
rs750544346 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347021 | GAGTTGTTTTGGTCT[C/T]AGTAATCTCAGCTCT | 10213 |
rs750544527 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161329335 | TTTTTTATATCTGTC[A/C]CATCTGTCATAAATA | 10213 |
rs750556887 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406352 | GTGTGAATAGCCACA[A/G]ACATTTTCAGTGCTT | 10213 |
rs750582465 | in-del | -/TAAGAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393851 | AAACTTAGGAACATC[-/TAAGAA]TAAGTACTCAGAATT | 10213 |
rs750584651 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161353228 | TCATCTTATCCTTCA[A/G]ATATTGTCTTTATAA | 10213 |
rs750584844 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161385093 | TTAACTTGTGCTCAC[-/T]TTTCAGTTTTAGTTT | 10213 |
rs750602334 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314266 | CTCTTTAGAAAACAG[G/T]TTATTGCAAAATTTT | 10213 |
rs750661527 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371092 | TCTTAATTTATACCC[C/T]GTTAGTGTGTTGTTT | 10213 |
rs750669069 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331120 | TGTATAGCTATATCA[C/T]TATAGGGAGATGATT | 10213 |
rs750672223 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390886 | AATTTGTGCTCCTCC[A/G]TATCATGCTTTGAAG | 10213 |
rs750703530 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336319 | CAGAGTCACCATATT[A/C]ATAAAACACTGCTTG | 10213 |
rs750704813 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315965 | TCCTGCCTCAGCCAC[C/T]TGAGTAGCTGGGATT | 10213 |
rs750709521 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377061 | ATTATCCTTGATCAA[C/T]TTGAACCCTGTAAAA | 10213 |
rs750741288 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394689 | GTAAACAAGTAAACA[A/G]AAATTTCAGGTCTTT | 10213 |
rs750782948 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376468 | GAATGTTTCTGCAAG[-/T]TTTGATAAGAACAAG | 10213 |
rs750792637 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320795 | CAATGGCATGATCTC[A/G]GTTCACTGTACCCTC | 10213 |
rs750800426 | snp | G/T | 1.66557e-05 | 0.00288575 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395032 | TAGACAATGAAGGGG[G/T]TATCCTCAAGGCAGA | 10213 |
rs750840013 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378523 | TTTTCATTTCAATAG[A/T]TATTTATTTTGCACT | 10213 |
rs750852530 | in-del | -/AAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402824 | TGGTTACAAACACAT[-/AAA]AAAGATGTTCAATCA | 10213 |
rs750886301 | snp | C/T | 6.77438e-05 | 0.00581956 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385606 | ATGTGTTAAAACTCT[C/T]TTAAATTTTAAAAGC | 10213 |
rs750892531 | in-del | -/GGCTGGAGTACAGT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345936 | CACTTCTGTCACCCA[-/GGCTGGAGTACAGT]GGCATGATCACAGCT | 10213 |
rs750917240 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322154 | TTGAGGCTCTGTGCC[A/T]GAAACTCAGGATAAA | 10213 |
rs750930076 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360503 | GGGATTATAGGTACC[C/T]GCCACCATGCCTGGC | 10213 |
rs750974424 | in-del | -/TGT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161350591 | CTTTGAACCTTGTAA[-/TGT]TGTGTCTTGATTAAT | 10213 |
rs750985383 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324421 | TGGGAAAAATGGGAA[A/T]AATGAGACTAAGGAG | 10213 |
rs751016068 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397170 | TGATATGCTTAGAAC[C/T]TGACTTTAGAAACAT | 10213 |
rs751068228 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383270 | AATTTTGGTCTGCAG[A/G]TTGTTGAACATGTTA | 10213 |
rs751116150 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161399742 | TTTAAATAAAAAAGA[A/T]TTTTTTTAGGAAAAT | 10213 |
rs751122995 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344881 | CCTTTGAAAAGGTTT[C/T]AATTTTGATGAAGTC | 10213 |
rs751162954 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312837 | TCTGCTAAATTCTGC[A/G]AAATGCAAGTCCCTA | 10213 |
rs751176015 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405132 | CTGACACTCATTTTT[C/G]TAGGCATCGTGTAGG | 10213 |
rs751198273 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348955 | CCAGGTAGTTGTCAC[A/G]TGGCTCTTTCTTCCT | 10213 |
rs751215905 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314843 | TTCCACCTTTTGGCT[A/G]TTGTGAATAGTGATG | 10213 |
rs751391555 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366180 | ATTAGGTGATAATAG[A/G]TGAAGAATTTGGTCA | 10213 |
rs751475896 | in-del | -/TC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371861 | AATATGCTAAATAAT[-/TC]TGAAAACAGATTAAC | 10213 |
rs751551292 | in-del | -/TAAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317154 | CCCGTTTTTAGCCTT[-/TAAA]AAGTGCTGTGTGTTG | 10213 |
rs751554585 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380934 | AAGAATCTAGAAACA[A/G]CCTAAGCAGTTGATA | 10213 |
rs751627557 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391441 | GGTTTTATGATAAGT[C/T]ATAAAAATATTTCTT | 10213 |
rs751632590 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352349 | TAATTCTGAGCTATA[A/G]ATACAGTTAAGAACC | 10213 |
rs751653469 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359316 | TAAGAATATAATTTT[A/G]TATGCTTATATATAT | 10213 |
rs751670681 | snp | A/G | 1.89626e-05 | 0.00307911 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367916 | ACAGTGAGTACTTTT[A/G]TGGTTGCCTGCTGCA | 10213 |
rs751687893 | snp | A/C | 2.03403e-05 | 0.003189 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367739 | AAGAAGAACCAGAGA[A/C]CTCAACGAAATTTGC | 10213 |
rs751703081 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401123 | TAATGTAAACTTATT[A/G]TATTGATAAATAAGT | 10213 |
rs751741192 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360250 | ACTGGAGTGCAGTGG[C/T]GAGATCATGACTCAC | 10213 |
rs751742303 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388597 | AAACACATTTTGTTT[A/C]TTTTCAGTTATTCTA | 10213 |
rs751792850 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161387536 | TTTTTTTTTACTCTT[A/C]TACTTAGTAGTAGAG | 10213 |
rs751798330 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345896 | GTTCATTCTTTTTAT[A/T]TTTATTTTTTCTGAG | 10213 |
rs751878913 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332675 | TGGAACCTTTTTCTC[C/T]TTTTGCAGTACCATG | 10213 |
rs751888040 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161355226 | ATATTTCAGCAGTGG[G/T]TGAAATTATGTCTTT | 10213 |
rs751934288 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405777 | CTTATGTAAAAATTG[A/C]CATAATGGTGATATT | 10213 |
rs752008774 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375363 | TTGCTAGAGACAGAA[A/G]TAATTCAACAAATAC | 10213 |
rs752032583 | in-del | -/TATT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391347 | AATATTTTATTGGAC[-/TATT]TAAAGACACATTTCA | 10213 |
rs752064451 | in-del | -/TTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338342 | GTAGGGTTAGGAGAG[-/TTT]TTTTTTTTTTTTTTG | 10213 |
rs752098236 | snp | A/G | 1.66081e-05 | 0.00288163 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395057 | GGCAGAAAAAGAATT[A/G]CTTTTTCTTTTATTT | 10213 |
rs752108449 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320651 | TTTGACAAATACTTA[C/T]GATGTTACTTTTGTA | 10213 |
rs752109999 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326191 | GCCCACCACCACGCC[C/T]GGCTAATTTTTGTAG | 10213 |
rs752120710 | in-del | -/TAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394959 | GGAGTTCATTTGAAT[-/TAA]TAAAGTTAAATCCAT | 10213 |
rs752123931 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376861 | TTTATAAAATAAAAT[C/T]GAGGAATGAATTTGC | 10213 |
rs752166405 | snp | C/T | 5.70923e-05 | 0.00534255 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408801 | GGAATAGAGGATTTA[C/T]AATTTTAAACTCTGT | 10213 |
rs752201739 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396581 | GAATCTAAAAAAGTT[A/G]AACTCATAGAAGTAG | 10213 |
rs752209056 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337434 | TTACATTAACCAGTA[C/T]CACGTGGTATGATTA | 10213 |
rs752262117 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322537 | TGGGATTACAGGCAT[A/G]AGCCTCCACGCCCAG | 10213 |
rs752266879 | snp | A/C | | | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161411983 | CTATCTTATAAACAT[A/C]CTTTTAGGATTTTGG | 10213 |
rs752274985 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383128 | GACATTAATGAGTCT[A/G]TTTTGATAGGTTGCT | 10213 |
rs752280284 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394432 | GATCTCTAAACTGAG[C/G]ATCAGAAAGATTGAC | 10213 |
rs752292329 | in-del | -/TA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376095 | TTTTATATATCTATG[-/TA]TATATATATACATAT | 10213 |
rs752301857 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312380 | AACCCCTGACCTCAA[C/G]TGATCTGCCCCCCTC | 10213 |
rs752355013 | snp | C/T | 3.87004e-05 | 0.00439872 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395067 | GAATTACTTTTTCTT[C/T]TATTTTTTAGATGTT | 10213 |
rs752389587 | snp | A/C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161308694 | TGAGTCACGTTGCCC[A/C/G]GCTGAGTTGCCACAG | 10213 |
rs752390726 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323913 | AACATATGTTGCCAT[A/G]ATTTGGCTACTTCGT | 10213 |
rs752421917 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359565 | GTATCTATACAGTGT[A/G]TAGTGCATTTTGCTC | 10213 |
rs752481119 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161370991 | CCTTTGTCACACATA[C/T]TCATTTCCATGTTTT | 10213 |
rs752483878 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161328797 | CAAATTCATGAAAAA[A/C]GGAGGGAGGCAAAAG | 10213 |
rs752492559 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314189 | CATTTGTGTACACTT[C/T]AGCATTTTTCCATGT | 10213 |
rs752494679 | snp | A/G | 5.17344e-05 | 0.00508572 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161367480 | TATTTGTTTCTAGGG[A/G]CCACCTACAGATGCT | 10213 |
rs752538326 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314215 | CATGTGTGAACTGCA[C/T]CAACATCATAAAACA | 10213 |
rs752559124 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315697 | AGTATGATAAAATAG[C/T]AAATTTTCAGGGTAT | 10213 |
rs752569076 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354236 | TGAATGATGCTGTGT[C/G]TATGTGTGTCAGATG | 10213 |
rs752583809 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352859 | TTGTATTCTGTGTTA[A/G]CACCTCCAGGGCCCA | 10213 |
rs752595131 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161408143 | GTTTGGGTTAATTTA[A/G]TTTTGATTATATTTG | 10213 |
rs752610813 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333271 | CTCAAATGCCTGTGC[A/G]TGTGATTAGATGTTA | 10213 |
rs752678587 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161367957 | TTTCTTTTCATTTTT[-/C]TTTTCCTATGCAAAC | 10213 |
rs752681880 | in-del | -/TGAAGTTTTTTTTCTCTAGACAATGAAGGGGGTA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395001 | ATGTTTTTTTTTTTT[lengthTooLong]TCCTCAAGGCAGAAA | 10213 |
rs752722392 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318984 | CTAACAGATAACTCT[A/G]TGGTAAGAATCTTAC | 10213 |
rs752767383 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358487 | GTGAGGGATAAAAAC[C/T]GTGCGCTGTCTCCTT | 10213 |
rs752834751 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343342 | TTTTGTGACTGGCCT[A/G]GCATAATGTCATTAA | 10213 |
rs752836502 | in-del | -/CTCT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406790 | CAAAGAGTTTGTGAA[-/CTCT]CTCTTTTAATTATTG | 10213 |
rs752915295 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332672 | CTGTGGAACCTTTTT[C/T]TCCTTTTGCAGTACC | 10213 |
rs752936589 | in-del | -/ACTC | | | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161411963 | AGCTAAATATTGTAT[-/ACTC]ACTATCTTATAAACA | 10213 |
rs752989051 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161364207 | TTGCTCATACCCCAG[G/T]GGTTTCTCTCCACGT | 10213 |
rs753012022 | snp | C/T | 8.4886e-05 | 0.00651428 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370082 | ATTTACAAAAATTAA[C/T]AATTTTTCTTTCTTT | 10213 |
rs753091352 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403388 | TGCCAGGGACTTGGG[C/T]AAGGCAGGAATGGGG | 10213 |
rs753110096 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318991 | ATAACTCTATGGTAA[G/T]AATCTTACCTTATTG | 10213 |
rs753140701 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406512 | CTGCAATCATTTCTT[-/A]ACGTTTTTCCTGGTA | 10213 |
rs753175951 | snp | C/T | 0.00107193 | 0.023126 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391201 | TAAATTTTTATCTTA[C/T]AGGAGGAAAAAAATC | 10213 |
rs753202688 | in-del | -/TG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161381373 | ACATTACTTCTACTC[-/TG]TGTAGATACCCATAG | 10213 |
rs753269696 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373477 | CTTTCAGTGTCAAGT[C/G]CTCTCATCTCTATGA | 10213 |
rs753297526 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317938 | CTTAGTTGTACTGTT[A/C]TTAACTTTTAAAATT | 10213 |
rs753330595 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352486 | CTAGAATAATAAACT[A/G]CACCAAGTTACAATC | 10213 |
rs753334932 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371140 | GTATTACTTGTTCTG[A/T]TCTGAGCATCTGAAT | 10213 |
rs753410102 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373199 | AATATGTATGTGTCA[-/C]CGTCTTAATGTTAAA | 10213 |
rs753422846 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405149 | AGGCATCGTGTAGGT[C/T]TGAAACTTTGGACTC | 10213 |
rs753443882 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396384 | AGTCAACCTAAGTGT[C/T]AATCAACAGACAGAT | 10213 |
rs753458636 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394792 | TTTAGGTATATTGTT[A/G]TTAGGGAAGACATCT | 10213 |
rs753486976 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322305 | AGAGACATGACCCCA[C/G]CTTGAGTCCCAGTGC | 10213 |
rs753524397 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320985 | CCTGCCTCGGCCTCC[C/T]AAAGTGCTGGGATTA | 10213 |
rs753539135 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337296 | TTGTTGAAATTAGAA[C/T]TGCTCTTTTTTGGTA | 10213 |
rs753584169 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331259 | ATGATGTCTTTGGAA[-/T]TTTTTTTTTTTTTTT | 10213 |
rs753587907 | snp | G/T | 2.45287e-05 | 0.00350197 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408824 | AACTCTGTCCTTTGT[G/T]TTTCATTCACAGGCT | 10213 |
rs753617360 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161384962 | CACAAGAAGTAAAAG[C/G]TATCTGACTAGAAGA | 10213 |
rs753668503 | snp | A/T | 1.72092e-05 | 0.00293331 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161367885 | GATTGATGTGTTTGC[A/T]ATGCCACAGTCAGGA | 10213 |
rs753672552 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342430 | GTTGTAATAAGATGA[C/T]CTTTTTTATTCCTTG | 10213 |
rs753705151 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368401 | GCAAAACAAAACAAT[A/C]GCAAACCTGAATATT | 10213 |
rs753705979 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366732 | GCATCTTGAGGGTAA[A/G]AACTATATGTCAGTT | 10213 |
rs753725672 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312113 | CAAATACGGAGTAGC[C/T]TGAAAAGGATTGAGC | 10213 |
rs753754143 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406751 | CATCTATGGCTGGGA[A/G]TACTTTTTACCATCT | 10213 |
rs753763543 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161309878 | ATTTTAATTTAGGCC[A/G]GGTGCGGTGGCTCAC | 10213 |
rs753814022 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348306 | ATGGACCATATGATA[C/T]CTGTCACAACTACTC | 10213 |
rs753815177 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314057 | ATTTTGTTGAAGATA[A/G]GATGGCCATCTTTCC | 10213 |
rs753815943 | snp | C/T | 9.38394e-05 | 0.00684915 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161391115 | ATAGGCATTAATTCA[C/T]GGACTAAACAGACAT | 10213 |
rs753852310 | snp | A/G | 4.10248e-05 | 0.00452888 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367559 | TTAAAAGTAGGTAAT[A/G]AATGTAGTTACTTGC | 10213 |
rs753949616 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161410243 | TGCCCTAAGACTTAT[G/T]TCTGAAATAAAAAAT | 10213 |
rs754076035 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161374872 | TATATTTATTAAAAA[C/G]CATTACTGCTTTAGA | 10213 |
rs754103777 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317872 | GGAATTTCATTTAGG[A/G]CATAGCGATTTTCAA | 10213 |
rs754213697 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346352 | ACATTGTCATTTTCA[C/T]CCCAAGAAGTTTTAT | 10213 |
rs754274380 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315558 | GCTTTCTACAACACA[A/G]TAAAAATGGAAGGAT | 10213 |
rs754314405 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402822 | AATGGTTACAAACAC[A/G]TAAAAAAGATGTTCA | 10213 |
rs754315283 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161309434 | TAAAATAGAGTTATA[A/G]TGTGAAAGTGATTTT | 10213 |
rs754376810 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389271 | AGTAGTGAGTGCATC[A/G]CGCAAATGTGCTTGG | 10213 |
rs754406025 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403819 | CTAACCCTTTCTCAC[C/T]TTTGAGACCCTCACC | 10213 |
rs754473944 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377296 | TACATAAAGAAATCT[A/G]TTTCCATTCCTGACA | 10213 |
rs754490947 | snp | C/T | 4.11142e-05 | 0.00453381 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395058 | GCAGAAAAAGAATTA[C/T]TTTTTCTTTTATTTT | 10213 |
rs754524950 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336430 | AAAACCGGATGAATT[A/G]TGGAAGCATATTATG | 10213 |
rs754544647 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390026 | TGAGCCACTGAGCCC[A/G]ACCCTGCATTTTATT | 10213 |
rs754556623 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378840 | CTTGTTTGTTGAGAG[C/G]ATTAGCAAGATAATT | 10213 |
rs754573976 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378829 | TAATACCTACACTTG[-/T]TTGTTGAGAGGATTA | 10213 |
rs754577889 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337331 | TAAACTAAATATTAA[A/G]AGATGTTTATTGTTA | 10213 |
rs754648235 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360806 | CTCCCAAAGTGCTAG[G/T]ATTACAGGCGTGAGC | 10213 |
rs754674981 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371439 | AGAAAGCTGCTGTCT[A/G]TTTACTTAAAAAACA | 10213 |
rs754711433 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336598 | TCATTTATTTTGAGA[C/T]GGAATCTTGCTCTGT | 10213 |
rs754732861 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321567 | TCTCCACAGAACTAC[A/C]CTTACTTCAGATGCC | 10213 |
rs754836233 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312861 | GTCCCTATCTCCAGT[A/G]TGATTTAGTAATGTG | 10213 |
rs754885218 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368412 | CAATAGCAAACCTGA[A/G]TATTTTTTTCCCAGG | 10213 |
rs754904731 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161351537 | AGCCCTTTGCCCCCA[C/T]TGTGTATTAATGAAT | 10213 |
rs754955884 | in-del | -/TTTTT/TTTTTTT/TTTTTTTT | 0.000212169 | 0.010298 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318796 | TTGTGCTTAGGAACG[-/TTTTT/TTTTTTT/TTTTTTTT]TTTTTTCTTTGTTTC | 10213 |
rs754982426 | in-del | -/AGT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161309213 | ACATTTCTCGTTTTA[-/AGT]AAAGTAGAAATCTGC | 10213 |
rs754986268 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394096 | TCTGCCTCAGCCTCC[C/G]AAGTAGCTGAGATTA | 10213 |
rs755055145 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161316641 | ATAGTATGAAAATGT[A/G]TTATTTTTAACAGAT | 10213 |
rs755056381 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161410361 | AAAAGCATGGCCAAG[A/C]AATAATTCCAATAAT | 10213 |
rs755108483 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343602 | GGAGGCCAAGGTGGG[C/T]AGATCACCTGAGGTC | 10213 |
rs755110619 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383478 | AACAGATCATGATAT[C/T]TACTGAACTAGTATT | 10213 |
rs755131448 | in-del | -/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400506 | AATCTTTTTTGAGAT[-/G]TACAACAATTTGAAA | 10213 |
rs755141880 | snp | A/G | | | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161412078 | ACATTTCTACCAACA[A/G]TTTTGAAACTGGGAA | 10213 |
rs755163761 | snp | G/T | 2.67913e-05 | 0.00365991 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367952 | ATGTGTTTCTTTTCA[G/T]TTTTCTTTTCCTATG | 10213 |
rs755175878 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317890 | TAGCGATTTTCAAGT[A/C]GAAAAAATTGCTTTG | 10213 |
rs755180195 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396884 | CCAGACTCAAGTGCA[A/G]TGGGGTGATCTCAGC | 10213 |
rs755185606 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358087 | AATTTTAAAAATTCA[A/C]AAAGTATTTGGAGGC | 10213 |
rs755229548 | snp | A/C | 6.08081e-05 | 0.00551365 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367745 | AACCAGAGACCTCAA[A/C]GAAATTTGCTTTGTG | 10213 |
rs755245152 | in-del | -/GTA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405587 | GTTTAATTAGTGATG[-/GTA]GTAGAAAAACTAGTT | 10213 |
rs755333765 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404072 | CACTATGCCTGGCTA[-/T]TTTTTTTTTTCTTTT | 10213 |
rs755348934 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347235 | TTGTCTGTTTTTTCT[C/T]TGCTTTAGGTGGGAA | 10213 |
rs755366481 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346358 | TCATTTTCATCCCAA[C/G]AAGTTTTATTTGGGT | 10213 |
rs755386821 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318677 | GAATTAATATGTGGT[A/G]TTAATTAACAGGAAG | 10213 |
rs755410984 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402838 | TAAAAAAGATGTTCA[A/G]TCAATTATTGGTCAT | 10213 |
rs755466616 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339499 | TTTTGTTAATGAATT[-/T]TTTTTTTTTTTTTTT | 10213 |
rs755471238 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331259 | ATGATGTCTTTGGAA[A/T]TTTTTTTTTTTTTTT | 10213 |
rs755489819 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371620 | AAGCCTGCTATAAAC[A/G]TTTTATTAATATTTA | 10213 |
rs755516937 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312644 | AACACTTTATTCATA[C/T]TGTCTGATAATATTT | 10213 |
rs755537756 | snp | A/G | 6.91109e-05 | 0.00587798 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367451 | CTCTGTGTTTGTTTT[A/G]ATAATAATTGATGTA | 10213 |
rs755588640 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336332 | TTAATAAAACACTGC[C/T]TGTATTTGAATATTT | 10213 |
rs755594273 | snp | A/G | | | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161391127 | TCATGGACTAAACAG[A/G]CATTATTACTCCATT | 10213 |
rs755596517 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346173 | TAGGCGTGAGCCACC[A/G]TGCTCGGCCATTTAA | 10213 |
rs755634341 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392614 | AATCCACTCATAAAC[A/T]CATCTGAAGGGCCCA | 10213 |
rs755654299 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161351357 | CTTTTATGAGTTGTT[C/G]TAGAATTTCTATCCT | 10213 |
rs755726976 | snp | A/G | 7.69586e-05 | 0.00620269 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395069 | ATTACTTTTTCTTTT[A/G]TTTTTTAGATGTTGC | 10213 |
rs755751604 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161319470 | GACCTCTAGATTTCT[A/G]CCTCAGGATAGTCTA | 10213 |
rs755756683 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400463 | TATAGGGCCACTTAT[A/G]CATGGATTTTTCTCA | 10213 |
rs755810167 | in-del | -/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403218 | ACTCAGTCATAAAAA[-/G]GAATGGAGTGCTGAT | 10213 |
rs755822677 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336362 | TTATGGCATATTGGT[C/T]GGAAACAAGGAAATG | 10213 |
rs755827651 | in-del | -/AT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372937 | ATGATATCTTGACTC[-/AT]GTGATGGTGGCTACT | 10213 |
rs755836519 | in-del | -/CTG | 7.42956e-05 | 0.00609445 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318811 | GTTTTTTCTTTGTTT[-/CTG]TTTTCTAGAAATATG | 10213 |
rs755849542 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383523 | ATGAAGTTTCACACC[C/T]GCTTATAATATTTCA | 10213 |
rs755943472 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326187 | AGGTGCCCACCACCA[C/T]GCCCGGCTAATTTTT | 10213 |
rs756077767 | snp | C/T | 1.7479e-05 | 0.00295621 | stop-gained | PSMD14 | GRCh38.p7 | 2:161318871 | ATGCCTGGACTGGGC[C/T]AGGTTAGTATATAGT | 10213 |
rs756132075 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349348 | CTTTGGCATTTTCAT[A/G]TATGCCTGGCTCACA | 10213 |
rs756139595 | snp | A/G | 3.42231e-05 | 0.00413647 | missense | PSMD14 | GRCh38.p7 | 2:161411312 | TTTAGGACCCCAAAC[A/G]TCATTTGGAGGAACA | 10213 |
rs756144239 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366177 | TGCATTAGGTGATAA[C/T]AGATGAAGAATTTGG | 10213 |
rs756176152 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161369605 | AAGACAGTACTCTAT[C/T]GCCAGAGAGATGATC | 10213 |
rs756205887 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388989 | ATTGAAAGACTACTT[A/G]AGGATATCATTTGAT | 10213 |
rs756246568 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161329336 | TTTTTATATCTGTCA[C/T]ATCTGTCATAAATAC | 10213 |
rs756303621 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331156 | TTTGCTTTAATTTGT[A/G]CCTGGTTTCACGGTT | 10213 |
rs756367553 | in-del | -/ATGTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393019 | TACATAAATTACTTA[-/ATGTT]ATGTTATGTTTATGT | 10213 |
rs756436351 | snp | C/T | 3.55019e-05 | 0.00421304 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161371229 | TGGTTGTTGGCTTTC[C/T]GGTGTGGATATCAAC | 10213 |
rs756466782 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378747 | TAACATTTACTGGTT[A/G]TGTCATTTCATTTAA | 10213 |
rs756514557 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345547 | ATTATAGGCATGTGC[C/T]ACTGTGCCTGGCCTC | 10213 |
rs756516416 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383870 | GTTCTTTTTTAGTAT[A/G]AGTGTGAGGAAATTT | 10213 |
rs756521184 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360554 | GAGATGGGGTTTCGC[C/T]ATGTTGGCCAGGCTG | 10213 |
rs756528516 | snp | A/G | 1.69657e-05 | 0.00291248 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370084 | TTACAAAAATTAATA[A/G]TTTTTCTTTCTTTCT | 10213 |
rs756621275 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161387773 | TCCATATTTCTTAAA[G/T]TTTTTTACAGTGAAA | 10213 |
rs756625304 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376470 | ATGTTTCTGCAAGTT[C/T]TGATAAGAACAAGCC | 10213 |
rs756661842 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326155 | AGATTCTTCTGCCTC[A/G]GCCTCCTGAGTATCA | 10213 |
rs756686627 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402623 | TTCAGCCTGGGCAAC[A/C]GAGCAAGGCTCTGTC | 10213 |
rs756692163 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346223 | ATTAACCCCATCTAG[C/T]GTATTTTTTATTTTG | 10213 |
rs756719240 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161364453 | ACCTAGGTCCATGAG[C/T]GCAGGCCTGGTGGTG | 10213 |
rs756770848 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404154 | CAAGTGATGCTTCCC[C/T]CTCAGCCTCCTGAGT | 10213 |
rs756818917 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391533 | ATTAGTAATATATTG[C/T]TCTGTAAATTTGAGA | 10213 |
rs756828972 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161362852 | TTGATTATTGCCTCA[C/T]ATATGATGGTCCCAA | 10213 |
rs756892012 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311165 | AATACAAAAATTAGC[C/T]GGGCATGGGGGCGTG | 10213 |
rs756903563 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332854 | TTCCAGTAATTTTGG[A/T]TGGGGATCTGACTGG | 10213 |
rs756967433 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161350938 | TTCAAATGTTTCTTC[C/T]CATCATTGCCTCTGC | 10213 |
rs756968893 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315176 | GGAGACATTTTTGAT[G/T]GTCACAGCTGGATAG | 10213 |
rs756977712 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397399 | ATCAAAGAGGAATTC[A/G]AAGTTTCCTGCCTGG | 10213 |
rs757015992 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161355866 | GAAACCCTATGTGAT[A/T]AAATTGTTCTGAGCT | 10213 |
rs757023562 | snp | A/G | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306507 | TTCGTTGAAATGACA[A/G]AACCGCAATTTTTTG | 10213 |
rs757028610 | in-del | -/AG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161369302 | TTTTCTTCTGACCCC[-/AG]AGTCAGTAAACTTTT | 10213 |
rs757051432 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322625 | GAACTCCTGACCTCA[A/G]GTGATCTGCCCACTG | 10213 |
rs757067299 | snp | C/T | 2.33855e-05 | 0.00341939 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408830 | GTCCTTTGTGTTTCA[C/T]TCACAGGCTGTAGAA | 10213 |
rs757087615 | in-del | -/ACTC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311987 | TTAAATTTAATGTTG[-/ACTC]ACTCACGATCTTCCA | 10213 |
rs757123015 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338938 | CTAGCTTTCATTACT[A/G]TAATTGTTTTGAGAT | 10213 |
rs757132935 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396838 | GTTTGTTTGTTTGTT[G/T]GCTTTTTGAGATGGA | 10213 |
rs757223041 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380978 | AGGTGATAAAGAGTA[C/T]TGGATATGGGTTAAG | 10213 |
rs757249742 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324494 | TCAAAAGGCTAGAGA[A/G]TAGATACATAAGAAA | 10213 |
rs757272268 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363203 | TGATGATCTGAGGTG[A/T]AACAGTTTCATCTCA | 10213 |
rs757316386 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383327 | ATGGCAGCAAATTCC[C/T]TTAATCTTAGTGTAA | 10213 |
rs757401883 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161387555 | TTAGTAGTAGAGAAA[A/T]ATTATGATTCACTGT | 10213 |
rs757405086 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161327145 | ATATGATTCCACTTA[C/T]ATGAGGTACCTAGAG | 10213 |
rs757469128 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388998 | CTACTTGAGGATATC[A/G]TTTGATTTAAACTTA | 10213 |
rs757527038 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391542 | ATATTGCTCTGTAAA[-/T]TTGAGAGGAATAACT | 10213 |
rs757530357 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313008 | ATGCTTACTATATGA[G/T]AAGCATTGTGTTAAA | 10213 |
rs757550569 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393579 | TTCTAAGCAAGTAGG[A/T]TAATTTTTCTAAACT | 10213 |
rs757616434 | snp | G/T | 1.854e-05 | 0.00304461 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385577 | ATCTATCCAGGTATT[G/T]CCTATATTTGATAAT | 10213 |
rs757617231 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161407021 | GATTGGTATTTTGAG[C/G]CAAATTCCAAAATTT | 10213 |
rs757623092 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338702 | ATTTAAAGTGTATAA[C/T]TTGTTAAGTTTTGAC | 10213 |
rs757634623 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375420 | ATACAATAAAGTATT[A/T]CTTGTATAACAAACA | 10213 |
rs757642237 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376923 | TTTTAGTTTTTAGCA[C/T]ATCCAAAAAACTGCA | 10213 |
rs757648986 | in-del | -/AAAG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376158 | AGGGCATAGAGTAAT[-/AAAG]AACACAGACTTAGGG | 10213 |
rs757657894 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161319247 | TCCTGCTTGCCAGAT[A/C]CAGAAAACTGACCCA | 10213 |
rs757664205 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402999 | GTTCCTCAAAAAGTT[-/A]AAACAGACAGTTCCC | 10213 |
rs757776897 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358627 | CCCTTGACTCATACG[A/T]TTTTCTCCTTAAGTT | 10213 |
rs757838664 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380535 | CCCCCTTTTCTCCCA[A/G]TATACTGAAGTTGTA | 10213 |
rs757848450 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343522 | TTGCTGCTATGAACA[C/T]TGGTGTAGAAATATC | 10213 |
rs757853993 | snp | A/T | 2.59798e-05 | 0.00360405 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371334 | AAAGGTAGAGTAGAT[A/T]CTATCTTTATTGCCA | 10213 |
rs757864884 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359349 | ATCCATAATTTAATT[A/C]TTTGAACTGGTAATA | 10213 |
rs757887849 | in-del | -/GTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338341 | GGTAGGGTTAGGAGA[-/GTT]TTTTTTTTTTTTTTT | 10213 |
rs757934695 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403200 | TACTTACAACATACT[A/G]TTACTCAGTCATAAA | 10213 |
rs757966662 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322550 | ATGAGCCTCCACGCC[C/T]AGCTAATTTTTTTAT | 10213 |
rs758018060 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324281 | CACACAAGCAATCAT[A/G]TTTTAAGTGCCTAGT | 10213 |
rs758020077 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161308695 | GAGTCACGTTGCCCA[A/G]CTGAGTTGCCACAGG | 10213 |
rs758096790 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161364229 | TCTCCACGTCCAGCC[A/G]TTTGTGTGTCCCTCT | 10213 |
rs758105441 | in-del | -/ATGC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342980 | TAATATACTCCATAT[-/ATGC]TCTCTGGACCTTTGT | 10213 |
rs758105497 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310150 | GTGAGACTTTGTCTC[-/A]AAAAAAAAGAGAAAA | 10213 |
rs758143274 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333073 | CTTTAGCATCTGTCT[G/T]GTACATTTTTGAAGG | 10213 |
rs758146695 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161309786 | ATCTTTTATTGATGC[G/T]TCACCTGTTGACTTT | 10213 |
rs758187298 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371016 | TGTTTTCTGGATAAT[A/G]TGGTGTACAATTTCA | 10213 |
rs758219602 | in-del | -/GT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338341 | GGTAGGGTTAGGAGA[-/GT]TTTTTTTTTTTTTTT | 10213 |
rs758277846 | snp | A/G | 2.18038e-05 | 0.00330173 | missense | PSMD14 | GRCh38.p7 | 2:161408840 | TTTCATTCACAGGCT[A/G]TAGAAGAAGAAGATA | 10213 |
rs758280543 | snp | A/G | 1.82171e-05 | 0.00301798 | intron-variant | PSMD14 | GRCh38.p7 | 2:161411292 | TCTTTCCTCATTTTT[A/G]TTCTTTTAGGACCCC | 10213 |
rs758302927 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354355 | GGCTCAAATGATCCT[C/G]CCACCTGAGCCCTCC | 10213 |
rs758311496 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395558 | TGAAAGGGACAAGGA[C/G]TAAGGGGATATAGAT | 10213 |
rs758358048 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337487 | GGTCATAGCTTTAAG[G/T]GGTTAAGATAGGATT | 10213 |
rs758369568 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161409855 | AATGAAATACAGTTC[A/G]TTTTATTTTCTCATC | 10213 |
rs758384915 | snp | A/C | 0.000214707 | 0.0103589 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367592 | TAGAGAACTCTGTTG[A/C]TTTCACTGTATCTTT | 10213 |
rs758405789 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161379345 | TATTTGTCACTTGTG[A/C]GTGTAGAAACACCGA | 10213 |
rs758456753 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388391 | TAATCCAGTGAGGTA[A/G]TGTAGGAACTAGTAC | 10213 |
rs758469354 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358576 | TACAACCTCATTAAT[C/G]TGACCACTCCTACTC | 10213 |
rs758483737 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398586 | TATTTGTAAATGAAT[A/G]TGCAGGTGAAAAAAT | 10213 |
rs758570185 | snp | C/T | 1.77988e-05 | 0.00298313 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318887 | AGGTTAGTATATAGT[C/T]TCTTGAGCATTTCCT | 10213 |
rs758574893 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400005 | CTCTATCTTGCATAT[A/G]TGTCAACATATTGTG | 10213 |
rs758738088 | in-del | -/TAAAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375882 | AATTTTTAAAAAAAT[-/TAAAA]TAAAAAGTTAGTGAA | 10213 |
rs758850145 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161356410 | ATGGTAGTTAGTTGT[A/G]TGTGTTTGAATTCAT | 10213 |
rs758890799 | in-del | -/CT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354148 | CTTGATTCTGGGCCC[-/CT]CTTTCCAGTTATGTT | 10213 |
rs758906232 | snp | C/T | 6.77147e-05 | 0.00581831 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385607 | TGTGTTAAAACTCTT[C/T]TAAATTTTAAAAGCC | 10213 |
rs758988977 | in-del | -/AC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366392 | AATAGAATTTAACAC[-/AC]ACACACACACACACA | 10213 |
rs758991543 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375267 | GCAAGATCTTATTCT[G/T]CCAATTATATACTGA | 10213 |
rs759041888 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161411167 | GTAACAATATACTAG[C/T]AAAGTTAAATTGTAA | 10213 |
rs759045857 | snp | A/G | 7.16461e-05 | 0.00598481 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367780 | CATCTCTTCCTTTCT[A/G]CAGATGTTAAAACAT | 10213 |
rs759061926 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372561 | AACAGTAATAGAAAC[G/T]GATATACTAGACCAT | 10213 |
rs759070051 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161409519 | GATGTTGGCAGAATC[G/T]TGATATTTCAGATGC | 10213 |
rs759129906 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397154 | TTTTTGATCAGAGGC[A/G]TGATATGCTTAGAAC | 10213 |
rs759186871 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393877 | ACTCAGAATTGTAAG[-/T]CCAATTTGAGAAACA | 10213 |
rs759196869 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161327863 | AATGAAAACTAAAAC[A/C]ACTATTAGATTAGTT | 10213 |
rs759208548 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380225 | ACCCAGAATTCTAAC[G/T]TAGGCAGGATTGACT | 10213 |
rs759254806 | snp | A/G | 6.32211e-05 | 0.00562197 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367464 | TTAATAATAATTGAT[A/G]TATTTGTTTCTAGGG | 10213 |
rs759285886 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346730 | TCATTATTTTCTACT[A/G]TTGAGGCTAGACCTT | 10213 |
rs759320914 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402183 | GTTTGCTTGCATCTC[C/T]AGTCTTTCCCTTTCA | 10213 |
rs759332098 | snp | G/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307804 | ATCATGAGTAAAATG[G/T]GATTGCCGATAATTA | 10213 |
rs759418633 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161370538 | GATTATGAATATTTA[A/G]TTATGTTTGTAGGCA | 10213 |
rs759499059 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389560 | CAATCAGTCACTGCT[C/T]CCTATGGAATTTCAT | 10213 |
rs759556182 | in-del | -/CTGT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371433 | TTACACAGAAAGCTG[-/CTGT]CTGTTTACTTAAAAA | 10213 |
rs759606298 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332508 | GTTTTATTTGAATAA[A/T]AGACTTGCCAATTAG | 10213 |
rs759635697 | in-del | -/TATAT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335322 | TCTGTGGGTTGGAAA[-/TATAT]TATATTTAGCTGCCC | 10213 |
rs759646117 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161316243 | AGATAAAATTTGGAT[-/A]ACAGGGTTAATCACT | 10213 |
rs759660723 | snp | G/T | 3.50822e-05 | 0.00418806 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371151 | TCTGTTCTGAGCATC[G/T]GAATGCCCTCTTTGT | 10213 |
rs759681274 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406185 | GAGGTTAATGGGTTT[A/C]GTAAAAGCCTCTGTA | 10213 |
rs759681452 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392164 | TTTTTTGATATTACA[A/G]TCTGAACCAGTTTCC | 10213 |
rs759736042 | in-del | -/AG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323991 | AAAAGCAGTGGAAAC[-/AG]AGCCCAAGAGATGAG | 10213 |
rs759770161 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393067 | AGCTGTTAACCTGCC[G/T]TCTTGGTAACAAAAG | 10213 |
rs759922750 | in-del | -/TT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161410480 | AATATATATTCCTTA[-/TT]TTTCAAAGCTCTGAA | 10213 |
rs759941486 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390753 | TTTTCATTTGAAATA[-/C]CCATGAGCCCCCTAG | 10213 |
rs759975567 | in-del | -/TTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161356763 | AAATATTCAAACTCC[-/TTT]TTTTTTTTTTTTTAC | 10213 |
rs759993004 | snp | A/G | 1.67041e-05 | 0.00288994 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395251 | ATCTTTGGAATATGT[A/G]TGATTAGATGCCAAG | 10213 |
rs760030890 | snp | A/G | 2.55216e-05 | 0.00357213 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408938 | ATGCAGTTGCATAAT[A/G]ACATGTTCTTATAGA | 10213 |
rs760036457 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365410 | TTCTAAGTACTGGTT[A/G]TATATATAATATTGA | 10213 |
rs760041733 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161325349 | AATAGGATGTATTTT[G/T]TTATAACTCCCAAAT | 10213 |
rs760063650 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310765 | AAATTAGTGTCATAT[A/G]GTGAGTAGGTGGTGA | 10213 |
rs760122779 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348352 | TGCTAAAGCAGCCAT[A/G]TATTACAAAAATGAA | 10213 |
rs760136738 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405137 | ACTCATTTTTCTAGG[A/C]ATCGTGTAGGTTTGA | 10213 |
rs760198377 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388542 | CTCCCTTCCTCTTTT[A/G]CCTTCTGCAACTCAG | 10213 |
rs760215645 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315409 | TGTGAAACATTTTCT[A/T]TGTTGCTTTTTTTCC | 10213 |
rs760229695 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368190 | AAAGTTACTTACCCT[A/G]TAATAGCAGAGTGTT | 10213 |
rs760243499 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161370685 | AAATTAATGTTAGCA[A/G]AAGGCTCAGCAGCTG | 10213 |
rs760297683 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161409326 | GAGTGAAGAGAAAGG[C/G]CTTTAAGTATTTGCT | 10213 |
rs760313970 | in-del | -/AA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321536 | ACTGTCAGACTCTGC[-/AA]GTTAAAGGCTCACTT | 10213 |
rs760319404 | snp | A/G | 7.28996e-05 | 0.00603693 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370225 | ATGGGAAATATTTAT[A/G]GAAACATACCTCAAA | 10213 |
rs760319416 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352419 | CGCTTTGAAATAGGG[C/T]CTTGCTTTTATTATA | 10213 |
rs760359035 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342237 | TAGGGGGAAACATTC[A/G]TTATCTGACCATCAA | 10213 |
rs760373650 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394763 | TTTTGTTTAAGGTAG[C/T]GTAGTGTGACTATTT | 10213 |
rs760429104 | snp | C/T | 1.67809e-05 | 0.00289658 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161367828 | AATGGAAGTTATGGG[C/T]TTGATGCTTGGAGAA | 10213 |
rs760450878 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359948 | CTTCTCGAAGCTTTT[A/G]TTTAACCACACAGCT | 10213 |
rs760494848 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359031 | GAATGTGCAGTGACA[A/C]AATCACAGCTCACTA | 10213 |
rs760497377 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373559 | TACTTAGGAATATAA[A/G]CTTATAAAAATGAAG | 10213 |
rs760509223 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161399749 | AAAAAAGAATTTTTT[A/T]AGGAAAATATACCAC | 10213 |
rs760509418 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161319968 | CTTTGTTGTCAGCCT[A/G]TTTCTTCATGATTCT | 10213 |
rs760549660 | snp | C/G/T | 4.73586e-05 | 0.00486591 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161367486 | TTTCTAGGGGCCACC[C/G/T]ACAGATGCTCCTGCA | 10213 |
rs760550738 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161387096 | TTTTGCCTTCCAGTT[A/G]GAACCTGTAAATATA | 10213 |
rs760572852 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311884 | CCTCCCAAAGAGCTG[A/G]GATTACAGGTGTGAG | 10213 |
rs760589797 | in-del | -/AA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373987 | ATGTTATTAGTGGTT[-/AA]AAAAAAAAAAATTAG | 10213 |
rs760629141 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326703 | GCATATACACTCATT[C/T]CTTAGTATCCTCGGG | 10213 |
rs760639021 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398891 | TATTGGGGAAAACAG[G/T]TAAGATGATTATTAT | 10213 |
rs760648997 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363767 | GTGGCCTGCTTCTTC[A/G]GTGCCCCACTGCTCA | 10213 |
rs760661312 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403802 | TTCATTCAATTCTCA[G/T]CCTAACCCTTTCTCA | 10213 |
rs760702275 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378494 | TAACCAAAAGTGCTC[-/T]TTTTTTTTTGAGGTT | 10213 |
rs760706739 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161309375 | GGTAATATAAGTTGA[C/T]AAAATATTATGGAAA | 10213 |
rs760762070 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161329049 | TTTAATTTGAAGGCG[A/G]TAATACTAGAGAGGT | 10213 |
rs760834824 | snp | G/T | 1.91521e-05 | 0.00309446 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391185 | GAACAGAAGGTAAGT[G/T]TAAATTTTTATCTTA | 10213 |
rs760891535 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337028 | GGAAGTAACTTATTC[A/G]AAGTCATTTAAAGAA | 10213 |
rs760916380 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313409 | GCTGGAGTGCAGTGG[-/T]TACCACCTTGGCTCA | 10213 |
rs760916548 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404804 | TGGCCATACATTCCC[A/G]TGGTTCCCCTGACTT | 10213 |
rs761002657 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332297 | TTTAAAAGAAGGTTT[A/C]CATTTCTTACTTTTT | 10213 |
rs761056871 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382899 | AATTAATTCTTGGGA[A/G]TTCTTTGTTCAGTGT | 10213 |
rs761070237 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354823 | TTTGATAGGGTCTCT[C/T]TATAACCAGATAATG | 10213 |
rs761101080 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331659 | ATAGGGAGACAGTCA[C/G]ATACTGTGAATAGGG | 10213 |
rs761113827 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161379887 | TATTTGGCAGGAATG[A/G]CTAGGTTCTAGTACC | 10213 |
rs761125467 | in-del | -/TATC | 0.000105781 | 0.00727181 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391093 | CTTTTTAAAATCATT[-/TATC]TATATAGGCATTAAT | 10213 |
rs761133757 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161387134 | CACAGTTTATATAGC[A/G]CCTACCAGAATGACA | 10213 |
rs761277437 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161362296 | TTACATCTGTATTTT[C/T]CCCTACTATAAAAGA | 10213 |
rs761292964 | snp | A/G | 2.14516e-05 | 0.00327496 | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411412 | ATAAAGCAACGAAAA[A/G]CGCTATTAATGATGC | 10213 |
rs761403883 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161384251 | ACTGATTAACTTGTC[A/G]TCATGTTTTAGTCTA | 10213 |
rs761435711 | in-del | -/GTAAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348536 | TAATAGTGGAAGTTT[-/GTAAA]GTATTGAAAAATGAA | 10213 |
rs761455233 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326626 | TTAGCAGCATTATTT[A/T]TAATAGCCAAGGGGT | 10213 |
rs761463053 | snp | A/G | 2.49822e-05 | 0.00353419 | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411432 | ATTAATGATGCCTTC[A/G]GTGTATATTCCTCTG | 10213 |
rs761493750 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406536 | CCTGGTAACTAGCCA[G/T]ATTAGAACTGTGAAT | 10213 |
rs761506699 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312530 | AGAAAGAAAAAGTGG[A/T]AAGTAATCAACTTTT | 10213 |
rs761568631 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375907 | AGTTAGTGAATGAAT[G/T]CTGTAAGAGCATACC | 10213 |
rs761634359 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333372 | TGAAATTTGGCCAGA[C/G]TTCTGGGTTACCAGT | 10213 |
rs761636544 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317580 | GATTCCATGGCCATA[C/T]CGTTTGTTTTCTTTT | 10213 |
rs761639544 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161374691 | AGTGGGGACCTCCTG[C/G]TGAATGTTGTATTAT | 10213 |
rs761687121 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343005 | GACCTTTGTGCTATA[C/T]GTTGAAAATCCATGA | 10213 |
rs761711448 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404764 | CATCATACCTTTGAA[C/G]TTCTGAAGTCTCTTT | 10213 |
rs761726604 | in-del | -/CTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318008 | CTTGATATTTCTTAA[-/CTT]CTTCTGTGAGGTTTT | 10213 |
rs761762846 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318743 | GACATACTGAGTGAC[C/T]GAAGGTGAATTATAT | 10213 |
rs761768567 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161379597 | ATTTTAACACTCTTC[A/G]TGATAGCAGTACTCT | 10213 |
rs761798942 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377508 | AATAACATGTAATAG[-/T]TTTATCACATTTATT | 10213 |
rs761812621 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322018 | CAAATGGGCCTGGCT[C/G]AAAGTCTTAGCCCTC | 10213 |
rs761854321 | snp | C/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161308096 | TGAGGAGGGCAATAA[C/T]AGTAGTGAACACCAA | 10213 |
rs761895939 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366865 | GTTTTAAAGGTAGTG[A/G]TTAGGATTTTGGAAG | 10213 |
rs761957051 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360257 | TGCAGTGGCGAGATC[A/G]TGACTCACTGCAGCC | 10213 |
rs761969060 | snp | C/T | 0.000124649 | 0.00789362 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391227 | AAATCTTTTTCAAAC[C/T]ATTTAAACTATTACC | 10213 |
rs761994490 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161308993 | ACTTTCCCATTGAAT[A/G]CGTTTGTTTTATCTC | 10213 |
rs762025873 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161308854 | CATGGGAACCTCTTC[C/T]ATCTATATAGAGAGA | 10213 |
rs762055599 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161341873 | AAATTAAAAAAAATA[A/T]ATATGTATATATAAA | 10213 |
rs762072475 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388952 | GAAGGCACTGGGGGC[A/G]CACAGCAGGTGAGTA | 10213 |
rs762085310 | snp | C/T | | | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161411883 | AATGATTTCCATTAA[C/T]GAGTGGCTACCTAAT | 10213 |
rs762143998 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403632 | GAATGAGGTCCAAAC[C/T]CCATTTGGCTCCTGC | 10213 |
rs762155611 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346923 | ATCATTATTAAGCTG[A/C]ATACTCAAAGAGGAC | 10213 |
rs762305361 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161353833 | GTGAATAAATAAAAA[C/T]GTAGATTATTTGTAT | 10213 |
rs762330119 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336819 | GGCCTCAGGTGATCC[A/G]CTGCCTCAGCCATCC | 10213 |
rs762367757 | snp | C/T | 1.89953e-05 | 0.00308177 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318922 | TGTAAACTACAAGCC[C/T]TTTTGTAGTTAGCCA | 10213 |
rs762379175 | in-del | -/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307419 | CACCCCCTCCTCCCA[-/T]TAAAAAATGAATAGA | 10213 |
rs762407692 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378297 | AAATACATGTCAGTG[C/G]TCTATGAGTTTCTCA | 10213 |
rs762416304 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344673 | ATATTTTTATCTGGT[A/G]TCATTTTCCTCCTGC | 10213 |
rs762448543 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358673 | AGCCTGGCCGGGCAC[A/G]GTGGCTCACGCCTGT | 10213 |
rs762537259 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161384114 | TATTAATTCATGTTC[C/T]GGGGATACTTGGCTT | 10213 |
rs762546056 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397423 | TGCCTGGGTGACCAG[C/T]AGTATGGTAGTACCA | 10213 |
rs762566763 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394259 | TTACAGGCATGAGCC[-/A]CTGTGCCCGGCCTAG | 10213 |
rs762567994 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382745 | ATAGTTTTTGTGTAA[A/C]GTTTTTTGGTTAAGT | 10213 |
rs762611768 | snp | G/T | 0.00387515 | 0.043847 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318807 | GAACGTTTTTTCTTT[G/T]TTTCTGTTTTCTAGA | 10213 |
rs762713086 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161325749 | GCTCTACCAGATTTC[A/G]AAACATATTTTAATG | 10213 |
rs762720838 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331917 | TCATATTATAGGGTC[A/G]AGTCACAGAACTAAC | 10213 |
rs762733922 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390025 | TTGAGCCACTGAGCC[C/T]GACCCTGCATTTTAT | 10213 |
rs762750848 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161330938 | TTCCCTAGTGTTGTA[A/C]ACGGAGCCTGAGTTA | 10213 |
rs762778322 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347791 | GCACTCACTGTGTGC[C/T]GGGTACTCTTCTAAG | 10213 |
rs762821961 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372855 | CAATATTTACAAGTA[A/G]TAATTAAAGCTTAAT | 10213 |
rs762833376 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161355534 | TGACATTTCCATTCT[C/T]ATTTTCTTTCTTTCT | 10213 |
rs762857155 | snp | A/G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365837 | ACTATTTTGAAATAT[A/G/T]CATTATTATTAACTG | 10213 |
rs762869755 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315753 | TACTATTTGATAGAT[C/T]TGTAATAATGTACAA | 10213 |
rs762912498 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161374199 | CATTGTGAGGCCATT[C/G]CTTAAGTTACTGTGG | 10213 |
rs762959507 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335668 | TTTTGATTTACAAAC[C/T]GTGTTGTAGTAAATA | 10213 |
rs762966651 | in-del | -/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336598 | TCATTTATTTTGAGA[-/C]GGAATCTTGCTCTGT | 10213 |
rs763005842 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320056 | TTGATCCTGAACCTG[C/T]TTCCATTCTTTTGTA | 10213 |
rs763007396 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161385429 | TTATCACTTGCTTTT[A/T]AAAAAAAAATTGACT | 10213 |
rs763027057 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326549 | CAGCAATTCAGCTTC[-/T]GGGTATGTGCCCAAA | 10213 |
rs763035887 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161399600 | TTTGCCTATAAAATA[-/T]TTTTTTTAAAATAAG | 10213 |
rs763092207 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376806 | AGATACCAATTCATA[A/T]CTTGGAATTCAGTGC | 10213 |
rs763125994 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354954 | AAACTTAGGTGTGCT[A/G]TATTGGAGGAACTCA | 10213 |
rs763212303 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404993 | ATGTATTATCATCTC[C/T]ACTGTCTGAGACCTT | 10213 |
rs763212609 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321747 | AATTTTGTTATCCAG[A/G]AATACAGATTAGGAG | 10213 |
rs763271415 | snp | C/T | 3.55676e-05 | 0.00421693 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395231 | TCTGCCATTTCTTCT[C/T]TATAATCTTTGGAAT | 10213 |
rs763338219 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310929 | TCTCAGTGCATGCCA[C/T]TAAATTTCTTGAGTC | 10213 |
rs763365184 | snp | C/T | 4.55882e-05 | 0.0047741 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395038 | ATGAAGGGGGTATCC[C/T]CAAGGCAGAAAAAGA | 10213 |
rs763369353 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161350668 | GAGTAAAAACAAAAT[A/T]AACTAAATTGAGGAA | 10213 |
rs763437201 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161367408 | ATCAAGTTTATACCA[A/C]ATGTAACTTGAATTT | 10213 |
rs763454215 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347987 | AATTATGTGAGCTTT[A/G]ACAAATCAATAAGAA | 10213 |
rs763458528 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161351911 | TTAGGGAAGTGCAGT[C/T]GTACTATGTGCCTGA | 10213 |
rs763536300 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314704 | AGCTAACTTGTAACA[A/T]GTACCAGTAAGTAGT | 10213 |
rs763537128 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393256 | ACACTTAATTATAGG[C/T]AGCTGTATAGCATAG | 10213 |
rs763575946 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393137 | CCCCCAGCCTTACTC[A/G]AGGGTCGCAAGGGAA | 10213 |
rs763628089 | snp | A/G | 6.55616e-05 | 0.00572508 | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411414 | AAAGCAACGAAAAAC[A/G]CTATTAATGATGCCT | 10213 |
rs763748782 | snp | A/G | 6.25085e-05 | 0.0055902 | intron-variant | PSMD14 | GRCh38.p7 | 2:161411263 | TTATCTACCAGTAAT[A/G]TGGTTCTGTTTTCTC | 10213 |
rs763772708 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348781 | AAAGGACACAGGAGC[C/T]TCAACCCAGCTGCTT | 10213 |
rs763778226 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382860 | TCAAAAAAATGGATT[-/A]TTTCCCCTACCAACC | 10213 |
rs763780674 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161384192 | AAAATAAAAGTAAAA[C/T]TCAGAGTTGATATTG | 10213 |
rs763847545 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310938 | ATGCCACTAAATTTC[G/T]TGAGTCAGCCCTCCA | 10213 |
rs763885310 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372917 | ATTAGTTCAACTTAG[A/G]TTTTATGATATCTTG | 10213 |
rs763912702 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365949 | GGTTACTACTACTTC[C/G]CCCAAACCTCTCATC | 10213 |
rs763954661 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161367991 | TCTCATCATATTACA[-/T]TTTTCTCTTTCCAGT | 10213 |
rs764002696 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161410111 | TCATTTTTAAAAATA[C/T]AGTTATTACCTCACT | 10213 |
rs764013813 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318312 | CTAATTCAGAGATCC[A/C]TAATCTGCTCACAAT | 10213 |
rs764090584 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396724 | CTAGCATGCATAGAA[C/T]GTGAGGGTGAACAGT | 10213 |
rs764096639 | in-del | -/TAAAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161399699 | GTCGTCAAAAAAAGT[-/TAAAA]TAAATAGAAAAATAT | 10213 |
rs764152082 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161362561 | TATGGAATCCTATTT[C/T]CTGAGCCCTTACACA | 10213 |
rs764208065 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335543 | CCATATCCATAGATA[C/T]AAAGCTGCATGTTTT | 10213 |
rs764268187 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401114 | GTAAACAGATAATGT[A/G]AACTTATTGTATTGA | 10213 |
rs764276615 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378125 | TCTTGTCATTGTAAT[C/T]TTCTAAAGAGGGTAA | 10213 |
rs764278853 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359256 | GGATTATAGGTGTGA[A/G]CCACTGTGCCTGGCC | 10213 |
rs764300080 | snp | G/T | 1.89932e-05 | 0.00308159 | missense | PSMD14 | GRCh38.p7 | 2:161371268 | GAGCTTTGAAGCCTT[G/T]TCGGAGAGAGCTGTG | 10213 |
rs764305818 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161391439 | TTGGTTTTATGATAA[A/G]TCATAAAAATATTTC | 10213 |
rs764314137 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344662 | TGTATAGATCCATAT[G/T]TTTATCTGGTATCAT | 10213 |
rs764357822 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161387455 | CAGCTTTCAAGTAGT[A/G]GGGATAAAAGTCTGA | 10213 |
rs764367094 | snp | A/G | 3.43838e-05 | 0.00414617 | missense | PSMD14 | GRCh38.p7 | 2:161385492 | CCTTCAGATTGATCA[A/G]TGCTAATATGATGGT | 10213 |
rs764459890 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161350804 | CTGAAGGTATTCCAT[A/G]TCTTGATTAATGGTA | 10213 |
rs764460974 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405013 | TCTGAGACCTTTCCA[A/G]TTACATGTTCATTAC | 10213 |
rs764515486 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333716 | AAGCTCCCAATGAGA[A/G]AAAGGTATCAATTTT | 10213 |
rs764546377 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312441 | GAGCCACTGCACCTG[G/T]CCAAAAATTGATTTA | 10213 |
rs764550907 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392334 | CAAGTCAGAAAGTGA[C/T]AAGTAATCAGTAGCA | 10213 |
rs764639988 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335678 | CAAACCGTGTTGTAG[G/T]AAATATCTCATTGAA | 10213 |
rs764660577 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342608 | GTTAGATTTTGAGAT[A/G]TTGTGTTTTGCTTTT | 10213 |
rs764671492 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161355166 | GCTAATCAAATTTTT[A/G]ATAAAGAAATATATC | 10213 |
rs764720651 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388793 | CATGAATAGCTTATA[-/T]ATAATCCGTAAGCCG | 10213 |
rs764761344 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376854 | ATAAATGTTTATAAA[A/G]TAAAATCGAGGAATG | 10213 |
rs764792370 | snp | G/T | 2.52121e-05 | 0.00355041 | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411433 | TTAATGATGCCTTCA[G/T]TGTATATTCCTCTGT | 10213 |
rs764912421 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338303 | GCATGTATTCACAGG[C/T]CCTATAACGCAGTTA | 10213 |
rs764919694 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397352 | TAAAGCATGGCACTG[G/T]TCGGATAGACGAAGT | 10213 |
rs764934504 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161362719 | AAATCCAAAGTCAAC[C/T]TGTGTTGCATTTTTT | 10213 |
rs765003705 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383065 | TTTTTTTTAATCTTA[C/T]GGTGGCATAATTAAC | 10213 |
rs765063565 | snp | C/T | 1.96578e-05 | 0.00313504 | intron-variant | PSMD14 | GRCh38.p7 | 2:161411280 | GGTTCTGTTTTCTCT[C/T]TCCTCATTTTTGTTC | 10213 |
rs765074631 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312309 | TCACCACGCCCAGCT[A/G]ATTTTTGTGTTTTCA | 10213 |
rs765124013 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372696 | AAAAATCCTTGATTG[G/T]TATTAGCTTTATGAA | 10213 |
rs765172532 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315686 | TAATGCCTCCTAGTA[C/T]GATAAAATAGCAAAT | 10213 |
rs765192346 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161399438 | AGAATTCCTATAAAA[C/T]ATTTATTTTATTTTT | 10213 |
rs765201539 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317905 | AGAAAAAATTGCTTT[C/G]TTGTCATTTTTAAAT | 10213 |
rs765204354 | snp | A/G | 1.78061e-05 | 0.00298375 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371134 | ATAAATGTATTACTT[A/G]TTCTGTTCTGAGCAT | 10213 |
rs765209346 | in-del | -/TT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315843 | TTTTTATTTTATTCT[-/TT]TTTTTTTTTTTTTTT | 10213 |
rs765332708 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333592 | GAGAATGAGAATGCA[A/G]TGTAAATGTTCAAGA | 10213 |
rs765409690 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332270 | AAGGTAGAGGTTACA[A/G]ATAGTACAACTTTTA | 10213 |
rs765449057 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358420 | TTTATGTCTAGGATT[A/G]GAAATATGAGACATA | 10213 |
rs765457974 | snp | A/G | 7.05667e-05 | 0.00593956 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318880 | CTGGGCCAGGTTAGT[A/G]TATAGTCTCTTGAGC | 10213 |
rs765539728 | snp | A/C | 2.10888e-05 | 0.00324715 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385600 | TTGATAATGTGTTAA[A/C]ACTCTTTTAAATTTT | 10213 |
rs765567791 | snp | A/G | 4.55425e-05 | 0.00477171 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395028 | TCTCTAGACAATGAA[A/G]GGGGTATCCTCAAGG | 10213 |
rs765596247 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161364121 | TCCACTGGAGTCAGG[A/G]CGCTGTCCTCCAACT | 10213 |
rs765612101 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310879 | GGTTTGTGTCAAGCT[A/G]CTTCTACCCACCTGC | 10213 |
rs765628170 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404936 | TTTCATAGTTTAGCA[A/G]TGCCAACAACTTTGA | 10213 |
rs765715293 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403895 | GAACTTTGTTCTTCT[A/G]TCAAATGAATTTAAA | 10213 |
rs765726356 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332518 | AATAATAGACTTGCC[A/T]ATTAGCCATCAAGTG | 10213 |
rs765870172 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349240 | AGTTCCCCTTTCTCT[A/G]GCCTCTCATTTGTTA | 10213 |
rs765873591 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161370712 | GCTGAGCAGAACAGT[A/G]CAAATTGGTTTTTGA | 10213 |
rs765901455 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315844 | TTTTATTTTATTCTT[-/T]TTTTTTTTTTTTTTT | 10213 |
rs765938297 | snp | C/T | 0.00239298 | 0.0345075 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318811 | GTTTTTTCTTTGTTT[C/T]TGTTTTCTAGAAATA | 10213 |
rs765984831 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403241 | GTGCTGATACATGCT[A/G]CTACATGGATGGACC | 10213 |
rs766033168 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161399783 | TGGGAAAGTAATTGA[C/T]ACATTTTTGGAGGCC | 10213 |
rs766067815 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344549 | TTTTGAGAAAGTGTC[A/G]TATTGTTTTTCACAG | 10213 |
rs766079128 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378794 | ACACTGCAGTTTCCT[C/T]ATCCATAAATTGATA | 10213 |
rs766087743 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354127 | TTATGAGACGTTCAG[C/G]TTCTGCTTGATTCTG | 10213 |
rs766120188 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322204 | AAAGACTTGTTTTCA[A/G]CCTTGACTTCATTAT | 10213 |
rs766120877 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161384961 | TCACAAGAAGTAAAA[C/G]GTATCTGACTAGAAG | 10213 |
rs766149137 | in-del | -/TCT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378493 | AGTAACCAAAAGTGC[-/TCT]TTTTTTTTGAGGTTT | 10213 |
rs766187992 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315842 | ATTTTTATTTTATTC[-/T]TTTTTTTTTTTTTTT | 10213 |
rs766221629 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312005 | CACTCACGATCTTCC[A/G]CTGGAAAAAAGTCCT | 10213 |
rs766298961 | snp | A/C | 3.70851e-05 | 0.00430595 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367911 | CAGGAACAGTGAGTA[A/C]TTTTATGGTTGCCTG | 10213 |
rs766303850 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345730 | ACAAATTTTGGTCAC[A/T]GTTTCTTAAATATTT | 10213 |
rs766330126 | in-del | -/TTTG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337153 | GGAAACGTGCTTTGT[-/TTTG]TTTGTTTGTTTGTTT | 10213 |
rs766353001 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312836 | TTCTGCTAAATTCTG[C/T]GAAATGCAAGTCCCT | 10213 |
rs766373475 | in-del | -/TTG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342324 | CCTGCTATTCCTACT[-/TTG]TTGAGACTTTTTTTT | 10213 |
rs766384207 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161329084 | ACAGTATAGATCTTG[C/T]AGGGCCCTGTAGAAA | 10213 |
rs766461322 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348112 | CTCTTGGAAAAACTT[G/T]TGGCAGAATCTGTTA | 10213 |
rs766488475 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368363 | ACTTTTTAAGCTTTT[C/G]TTATTTAAAATGTTA | 10213 |
rs766511855 | in-del | -/TTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315842 | ATTTTTATTTTATTC[-/TTT]TTTTTTTTTTTTTTT | 10213 |
rs766516163 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390956 | GTAGCTAAGAAGAAT[A/G]CTTTAATTTCATCTT | 10213 |
rs766562384 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161355831 | GACAGTTGTTGGATC[C/T]GCAAACAGAAATGTA | 10213 |
rs766579028 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161374821 | ACTTTGGGCAAAATC[A/G]TAAAACTAGCATACA | 10213 |
rs766604064 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373240 | AAAAAATAATATATC[G/T]AAAATTTATGAAATC | 10213 |
rs766628295 | in-del | -/TCT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405098 | TTCATGACAGTTCCC[-/TCT]ACCAATTTGGTTATA | 10213 |
rs766716254 | in-del | -/TACT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161353766 | GGGCAGGGACTTTCC[-/TACT]TGTGTGTAGCTAGTA | 10213 |
rs766732246 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380011 | TGTGAGTCAGTCATG[A/C]GCTCCACAGCAGGTT | 10213 |
rs766735116 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322268 | TTCTTGTACTATGAT[A/G]CTGATTTTTATGTTG | 10213 |
rs766746800 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161362385 | TGGATTCGGATCCTG[A/G]TTATTTACATTATTT | 10213 |
rs766750846 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323186 | CTGTACTGGAATTTT[G/T]TAAACTGCCAAGTCT | 10213 |
rs766781062 | snp | C/T | 3.33695e-05 | 0.00408456 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395240 | TCTTCTTTATAATCT[C/T]TGGAATATGTATGAT | 10213 |
rs766833028 | in-del | -/TTATACT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161409944 | CACCAACTTGGAGCC[-/TTATACT]TTATAGAATTCAGTA | 10213 |
rs766865070 | snp | C/T | 1.66369e-05 | 0.00288412 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395044 | GGGGTATCCTCAAGG[C/T]AGAAAAAGAATTACT | 10213 |
rs766882993 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321415 | CCAATTTTGATGAAC[A/G]AAATGTCCAAGACAT | 10213 |
rs766907446 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326663 | AACTCAGATGTCCCT[C/T]AACAAATGAATGGAT | 10213 |
rs766947679 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363837 | TCTGACCCCACAGCA[G/T]TGTCTAGGATTGAGT | 10213 |
rs766992084 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402670 | ACAAAACAAAAATGA[A/G]AAGAAAGTATACAAG | 10213 |
rs767143458 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386745 | TCATACTGCTTCATT[A/G]TTTTTTGCAAAAGGT | 10213 |
rs767153152 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406544 | CTAGCCAGATTAGAA[C/T]TGTGAATGAAGACAA | 10213 |
rs767231399 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368030 | TTAATCATAAGTTTG[A/G]TAGAAATTTTTAGAT | 10213 |
rs767240057 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352244 | CTTGGGGAGCTAAAT[A/T]AAAAAAGATTCCTGA | 10213 |
rs767261264 | snp | A/G | 5.23903e-05 | 0.00511785 | missense | PSMD14 | GRCh38.p7 | 2:161367479 | GTATTTGTTTCTAGG[A/G]GCCACCTACAGATGC | 10213 |
rs767314401 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358013 | TATGCTCTTGATTAA[A/G]CACCAGAAAAAAGAC | 10213 |
rs767330538 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161367043 | GAAGTCTTCTTTCCC[C/G]TTCTCCTCCACTGTT | 10213 |
rs767349398 | snp | C/T | 0.00059794 | 0.0172804 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318818 | CTTTGTTTCTGTTTT[C/T]TAGAAATATGGACAG | 10213 |
rs767358197 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337667 | TTAGTTTATGGTGAC[A/G]GTCCCATGGCTGCCA | 10213 |
rs767360185 | snp | G/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306660 | GACATATGCACACCC[G/T]AAGCACCTTCTACAG | 10213 |
rs767415496 | snp | C/G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318753 | GTGACTGAAGGTGAA[C/G/T]TATATAGATAGCAAT | 10213 |
rs767462519 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161399687 | TAGCCTTTTTAAGTC[A/G]TCAAAAAAAGTTAAA | 10213 |
rs767466715 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404812 | CATTCCCGTGGTTCC[C/G]CTGACTTTTTGGCAA | 10213 |
rs767518734 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161355386 | GAGATGAAAGATGCA[G/T]TATATGTATATTTTT | 10213 |
rs767542398 | in-del | -/AGTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383750 | ATATTTACTGTTAAC[-/AGTT]AGGGTGGCAATTCTT | 10213 |
rs767582520 | snp | A/G | | | utr-variant-5-prime | PSMD14 | GRCh38.p7 | 2:161308325 | CGCCGGGCCGCCCGC[A/G]CCGTCTGTCCCAAGA | 10213 |
rs767606146 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403638 | GGTCCAAACCCCATT[C/T]GGCTCCTGCTTGCCT | 10213 |
rs767623983 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161384570 | TTAGTATATGATCTT[G/T]CTGTAAGATTGTTTC | 10213 |
rs767696857 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388953 | AAGGCACTGGGGGCA[C/T]ACAGCAGGTGAGTAA | 10213 |
rs767712024 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161329139 | GCTATTAGAGATGCT[A/G]AGCAAAGGAGTTATG | 10213 |
rs767725954 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346145 | ACCTTGGCCTCCCGA[A/G]GTGCTGGGATTATAG | 10213 |
rs767758513 | snp | A/G | 0.000276577 | 0.0117564 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161371175 | TCTTTGTTTCAGGCC[A/G]GAGATGGTTGTTGGT | 10213 |
rs767786577 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390701 | TTCCAGATTAATGTG[A/G]GTAAAGAAACAGCTG | 10213 |
rs767786925 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371026 | ATAATATGGTGTACA[A/G]TTTCAGGGTTTCTAA | 10213 |
rs767845030 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161308859 | GAACCTCTTCCATCT[A/G]TATAGAGAGAATCCT | 10213 |
rs767865859 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393611 | AACCCCCATATACCT[C/T]CAAGTACATCTTCAG | 10213 |
rs767872613 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336855 | GCTGGGATTATAGGC[A/G]TGAGCCACCGTGCTC | 10213 |
rs767896201 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311580 | GATGCTGAAATTAGG[-/A]AGACTCCATAATAGA | 10213 |
rs767901341 | snp | A/G | 2.61982e-05 | 0.00361918 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408939 | TGCAGTTGCATAATA[A/G]CATGTTCTTATAGAG | 10213 |
rs767901526 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394449 | TCAGAAAGATTGACA[C/G]AAGGTCACTCAATAA | 10213 |
rs767948952 | in-del | -/T | 7.97353e-05 | 0.00631358 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395064 | AAGAATTACTTTTTC[-/T]TTTTATTTTTTAGAT | 10213 |
rs767976952 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360264 | GCGAGATCATGACTC[A/G]CTGCAGCCTTGACCT | 10213 |
rs768026623 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322091 | AAGCTATCTAGGGGT[A/G]TGCACTAAGTCACAG | 10213 |
rs768057617 | in-del | -/AGTG | | | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161411900 | AGTGGCTACCTAATT[-/AGTG]AGTAACTCAGAAAAA | 10213 |
rs768141115 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358834 | TAATCCCAGCTACTT[C/G]GGAGGCTGAGGCAAG | 10213 |
rs768154015 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389754 | AATTTCCTGACATGT[A/G]TTGTGGCATAGTATG | 10213 |
rs768199314 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161319581 | ATTAACAAAAGAAAT[A/G]ACTATGTGTATTTCT | 10213 |
rs768220307 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386506 | GGCAGTCACTCATCT[A/G]TAATCTTCATCAAAG | 10213 |
rs768224815 | in-del | -/AAACA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402643 | AAGGCTCTGTCTCTT[-/AAACA]AAACAAAACAAAACA | 10213 |
rs768231007 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359693 | AAGGACATCTCAAGT[C/T]TTCTTTCCATTTTCT | 10213 |
rs768313681 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343933 | ATTCAACCAACGTTT[A/G]CATCTGTACTGAACA | 10213 |
rs768342931 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405639 | CATAATATTGTTTAT[A/G]TAGTCAATACTTTAA | 10213 |
rs768364737 | snp | C/T | 1.6593e-05 | 0.00288031 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371339 | TAGAGTAGATTCTAT[C/T]TTTATTGCCATCTAC | 10213 |
rs768372883 | in-del | -/TAAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347558 | AAAATCTGTTCAAAT[-/TAAA]TAGTTAATTGAAACC | 10213 |
rs768396216 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324481 | TGTCAAGGCATATTC[A/C]AAAGGCTAGAGAATA | 10213 |
rs768400366 | snp | A/T | 5.99107e-05 | 0.00547282 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370206 | ATGATCAGTTAAAGA[A/T]ATAATGGGAAATATT | 10213 |
rs768485692 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318545 | AGAAAATATAATTAA[C/G]TTAATGATAGCAAAG | 10213 |
rs768492980 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401674 | TATATGATCTTTATT[A/G]TTCATCTCTATTTCA | 10213 |
rs768494907 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404528 | CCCTTTGCCCCTCTC[C/T]CTTCCTTGAGGCTAA | 10213 |
rs768541299 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349521 | TGTGGAGTTCTTTCA[A/T]TTATTTCAGTACACT | 10213 |
rs768614690 | snp | A/G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354630 | ATATTTCACACACAC[A/G/T]TAGAAACTTTGTTTT | 10213 |
rs768620786 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310936 | GCATGCCACTAAATT[G/T]CTTGAGTCAGCCCTC | 10213 |
rs768621537 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375780 | TTCACATCTGTAATC[C/T]CAGCACTTTGGGAGG | 10213 |
rs768663621 | in-del | -/TG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343197 | CCCAAACTGAAACTC[-/TG]TACCCATTAGACCAT | 10213 |
rs768721299 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161334434 | TCTCTCTCCACAGCA[A/G]AAATGTCCAGTAGTT | 10213 |
rs768817741 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337735 | AAAGTGTATAAACAG[A/G]TACATTTGCAGTAAT | 10213 |
rs768841698 | in-del | -/AAAT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397888 | AGATTAGATAAAGAG[-/AAAT]AAATCGCTCACCGTA | 10213 |
rs768868928 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322789 | TGTTTTTGAGGCCAC[G/T]TGGTCTTAGTTGTTT | 10213 |
rs768898927 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161327420 | TAAAAGTTCAGTTAC[C/T]GTATCTTTAAAATAA | 10213 |
rs768954382 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161379560 | ATAGTTATAACTTGA[G/T]TTTTAGGGTAACTTT | 10213 |
rs768963336 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337546 | AAAGTATCTCTGCAC[C/T]TAATCAATATTTTAG | 10213 |
rs768983024 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161369742 | TGTAGAACTTTGGAT[A/G]AGGCTCATTTTAGTC | 10213 |
rs769006281 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358492 | GGATAAAAACCGTGC[A/G]CTGTCTCCTTTCCGC | 10213 |
rs769036095 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373187 | AATTTCATTTAAAAA[-/T]ATGTATGTGTCACGT | 10213 |
rs769102842 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161408724 | TTCAGTAAATTATTT[C/G]AATAAAAGTTGTATG | 10213 |
rs769104684 | snp | C/T | 1.95593e-05 | 0.00312718 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318783 | TTGAATAAACATTTT[C/T]GTGCTTAGGAACGTT | 10213 |
rs769176073 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161407457 | AGTAGATACAATACC[C/T]ATTCACTATCTTTTC | 10213 |
rs769229022 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161381360 | ATAAATTCTTAAAAC[A/C]TTACTTCTACTCTGT | 10213 |
rs769233622 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395949 | TAGCATCACCTAGAA[C/T]CTTGTTAGAAATGCA | 10213 |
rs769287778 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161370487 | AATTGAAAGAGCTTG[-/T]TATGTTCCATGTATT | 10213 |
rs769295037 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375633 | CTTTTTTCCACAGAT[A/G]TTAGAATGTAAAATG | 10213 |
rs769323638 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161361080 | AAATGTGCTTCTTCA[C/T]CCAGATCAAATAGGC | 10213 |
rs769339271 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318468 | GAAGGAAATTCAATC[A/G]TACATATGATAAGCA | 10213 |
rs769358356 | in-del | -/AA | | | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161411792 | CTAGAAATCTCACAC[-/AA]AGATATGTTTCCGTT | 10213 |
rs769362199 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161374021 | CAATGAGATTGCTTT[A/G]CCAAAGTCAGACCAT | 10213 |
rs769391887 | in-del | -/AAC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161364641 | GTGAGCATGTAGGAA[-/AAC]AACAGCCTTAGTCAC | 10213 |
rs769426015 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317479 | GGAATAGACTGGAAG[C/T]GGGGCTTGGGTGGCG | 10213 |
rs769446224 | in-del | -/CT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402064 | TAATATTCTTGACTC[-/CT]CTCTCTTTCTCACAT | 10213 |
rs769459050 | snp | A/G | | | missense | PSMD14 | GRCh38.p7 | 2:161411381 | TAGCAGCTATGTTGG[A/G]TACTGTCGTATTTAA | 10213 |
rs769520114 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310217 | ATTTTCATACTGGCC[A/G]TGTAAACCATGTGCT | 10213 |
rs769575932 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347656 | TTATATTGCTTTATG[G/T]ATACTTAAAATTGAA | 10213 |
rs769584724 | snp | C/T | 9.16212e-05 | 0.00676773 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161391124 | AATTCATGGACTAAA[C/T]AGACATTATTACTCC | 10213 |
rs769615421 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161308960 | GACCGGGAAAACAAG[C/G]GAGAGAGAGTAGAAT | 10213 |
rs769623477 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342561 | ATCTTTATTTAACCT[A/G]TTTGAAATAAGTTTC | 10213 |
rs769708334 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386253 | TGTTTTTAAACGCAC[C/G]ACAGTCTGTGTCTAT | 10213 |
rs769708507 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368662 | GAAAAATATGCATGT[A/C]TTTTTCCAAGCGATA | 10213 |
rs769760952 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347758 | AACACTAAAAAATAA[A/G]CAGTTAATATTTGTG | 10213 |
rs769825521 | in-del | -/AAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383976 | TTTTATTGCTTTTTT[-/AAA]AAAGAGAATATGTTT | 10213 |
rs769854913 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161351787 | AGCTGATACAGCGCT[A/G]TCATTGAACACTGAC | 10213 |
rs769888305 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376687 | GAATATATTACTTTG[-/A]AACTTGGGCCTATGA | 10213 |
rs769899918 | snp | C/T | 2.05501e-05 | 0.00320541 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161408866 | AGATAAGATGACACC[C/T]GAACAGCTGGCAATA | 10213 |
rs769919540 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320003 | TTTTATAACACCTGT[A/G]TAACTCATTCTCTCA | 10213 |
rs769940034 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161353409 | AAAACAACCATTGAA[A/G]TTTAAACAGTATTCA | 10213 |
rs770065921 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383903 | CTTCTATATTTTTAA[C/T]AATTGTTTGAAGTTA | 10213 |
rs770133543 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392724 | TAATTGCCTGCCTGT[A/G]TACCACAGTTTACTT | 10213 |
rs770179261 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395679 | GCATATCATACATGT[A/G]TACATATAGATTGCA | 10213 |
rs770198750 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337194 | ATCTGAGTACCTAAA[A/C]GTCTCGTTTGGGAGT | 10213 |
rs770199420 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400313 | AGCTTCAGCCATCTC[A/T]TCTGGGTTTCATGCA | 10213 |
rs770250594 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343749 | TGGAGAATCGCTTGA[G/T]CCTGGGAAGTGGGGG | 10213 |
rs770289012 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386427 | GTTGTGGCTTTGACA[A/G]TTAACCATGGTTAAG | 10213 |
rs770298644 | snp | C/T | 1.87763e-05 | 0.00306396 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367770 | TTTGTGTCCACATCT[C/T]TTCCTTTCTACAGAT | 10213 |
rs770338100 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312388 | ACCTCAAGTGATCTG[C/T]CCCCCTCGGCCTCCC | 10213 |
rs770352902 | snp | G/T | 2.00483e-05 | 0.00316603 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367751 | AGACCTCAACGAAAT[G/T]TGCTTTGTGTCCACA | 10213 |
rs770376335 | in-del | -/TGTTC | 1.77849e-05 | 0.00298197 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371133 | CATAAATGTATTACT[-/TGTTC]TGTTCTGAGCATCTG | 10213 |
rs770387443 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406229 | ATTGGAGGGGATTAT[A/G]ATCACATAACAGACC | 10213 |
rs770440271 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347409 | CCAGTCTCCTGAGTA[C/T]CTGGGACTACAGGCA | 10213 |
rs770479974 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315452 | TAAAATGAAAAATTC[C/T]GATTTCTTAACTGTG | 10213 |
rs770480815 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395619 | ATTTATTTTATGAAC[A/G]TTTCCATTATTTAAT | 10213 |
rs770518079 | snp | C/T | 1.69548e-05 | 0.00291154 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367428 | AACTTGAATTTTAAA[C/T]TCATAAACTCTGTGT | 10213 |
rs770519109 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331537 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 10213 |
rs770531796 | in-del | -/TT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161356764 | AATATTCAAACTCCT[-/TT]TTTTTTTTTTTTTAC | 10213 |
rs770536020 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373806 | AGATAAGCCTGGATT[A/C]TTTCTTGGTAATCTC | 10213 |
rs770544114 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161410986 | GGTATACATATATAA[A/C]TGAAATTTTTTAAAA | 10213 |
rs770571524 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161330839 | ATAATAAAAATTATG[A/G]TAGTTGTACTTTTCT | 10213 |
rs770573437 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372443 | TTGAAGTTGAATGTT[C/T]TCTGACATCATGTCA | 10213 |
rs770574153 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317198 | TTGATTTGAGGAATT[C/T]CAATGAGTATTTGAT | 10213 |
rs770694293 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354528 | TTGCAGTGGAGCACG[A/G]TGATTGTTACCCAAA | 10213 |
rs770703501 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161361736 | CTGAAGAAAGGTAAG[G/T]TGAGTGAACCAGTGG | 10213 |
rs770743074 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359963 | GTTTAACCACACAGC[C/T]AAAGTGGTAGCACAT | 10213 |
rs770749334 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357771 | GGCATTGTATGAAAG[A/G]CGAGACTATTTTATG | 10213 |
rs770751299 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321532 | GGTTACTGTCAGACT[C/T]TGCAAGTTAAAGGCT | 10213 |
rs770836369 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388575 | CTCCACTCTAGAGGG[A/C]ACCACAAAACACATT | 10213 |
rs770850862 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401088 | GCCATTTCAGACAGG[A/C]AATTCACCTTGTAAA | 10213 |
rs770887085 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380448 | ACGTTCAAAACTTGT[A/G]GATTTACTCTTTGAA | 10213 |
rs770898643 | snp | C/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307500 | TATGAGTAAAATAAT[C/T]TTTGTGTTTTTAAAG | 10213 |
rs770901716 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365276 | TTGCTTCCTCTCTCT[C/T]GAGGTAACTCTAGTT | 10213 |
rs770905107 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393465 | GCCAAAGGAAGGGAA[-/T]TGGAGGAGTTTTGTA | 10213 |
rs770919923 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403320 | ATATGATTCAATTTA[A/T]ATGAAAAAAACAGAC | 10213 |
rs771009267 | snp | A/C/T | 0.000358982 | 0.0133933 | synonymous-codon, missense | PSMD14 | GRCh38.p7 | 2:161391155 | ATTACTATTAACTAT[A/C/T]GGAAAAATGAACTGG | 10213 |
rs771019572 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161308851 | CATCATGGGAACCTC[C/T]TCCATCTATATAGAG | 10213 |
rs771054705 | in-del | -/AAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371053 | TAATGGTGCTTTTTC[-/AAA]ACACCTGTGTGTTTT | 10213 |
rs771070792 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161367166 | CCAACAGCATTTCAC[A/G]TATACACACTGTGGT | 10213 |
rs771154959 | snp | C/T | 0.000128333 | 0.00800938 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161411388 | TATGTTGGATACTGT[C/T]GTATTTAAATAAAGC | 10213 |
rs771180491 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347340 | ATTTTTTGGGAGAGG[A/G]GGTCTTGCTATATCA | 10213 |
rs771208713 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161399004 | AAGAATTATGTAGGT[A/G]GTAAACAGTTATATA | 10213 |
rs771235593 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161316798 | AATTTGTTAAATATG[C/T]TTCCTCTTTGCTGTG | 10213 |
rs771247890 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392913 | TTTGGAAATGTCTAG[C/T]TAATTACATCAATTT | 10213 |
rs771252284 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406059 | TCCTTAAGAGTGTTA[G/T]TGAAGTGCCAAAGAT | 10213 |
rs771287595 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397111 | CTGGGATTACAGGAA[C/T]GAGCCACCGTGCCTG | 10213 |
rs771291739 | snp | G/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307870 | TGTAAACTAAACTCG[G/T]CTTAAAATAGGTGGT | 10213 |
rs771295286 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333482 | GACCTACCAACTCAC[A/T]ATGAAAGGCAGTATA | 10213 |
rs771375579 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398616 | TGAATTGTGAAGAAC[A/G]TTTTAAGAATAGCAT | 10213 |
rs771377612 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382729 | ATTATATATTAAGGA[G/T]ATAGTTTTTGTGTAA | 10213 |
rs771509399 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368536 | TTGTTTGATGCATTA[G/T]ACTTGTGTTGATAGA | 10213 |
rs771520087 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342408 | GAGATGATTATATGA[C/T]TCCTTTGTTGTAATA | 10213 |
rs771541023 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345481 | CTCCTGACCTCAAGC[A/C]ATCTGCCGACCTCAA | 10213 |
rs771556254 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354485 | TTTTTTTATAACAAA[A/G]GTAGTCGAGCATTGT | 10213 |
rs771608548 | snp | C/T | 3.84667e-05 | 0.00438542 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161370145 | TCCAGTGTTCCAAGC[C/T]AAAATGTTGGATATG | 10213 |
rs771631483 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161329965 | GTAAAAGGGACATAA[A/G]TTTTCCATAGGTACA | 10213 |
rs771727168 | snp | C/T | 1.71202e-05 | 0.00292572 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161367798 | GATGTTAAAACATGG[C/T]CGTGCTGGAGTTCCA | 10213 |
rs771764898 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313658 | CCCAGCCTAAATACA[A/G]GTGTTTATTCTGTAT | 10213 |
rs771772718 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394206 | CGAATTCCTGACCTC[A/G]ACTGATTCACCCTCC | 10213 |
rs771834249 | in-del | -/TTATAATT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161410443 | ATATAATCATTTAAA[-/TTATAATT]TTATAATTTTTCTAT | 10213 |
rs771835063 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161390059 | CATCTGTCAAAATAC[A/C]AATTGAATTGCCCTA | 10213 |
rs771862726 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377711 | TGCATTTTGAATGAT[A/G]TAAATGTGCTTCAAA | 10213 |
rs771888055 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389379 | TTCTCTACCAGGCTG[A/G]TTCACCTCCTAATGT | 10213 |
rs771890059 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161370013 | TAGGTATCAAAACCT[A/G]TAAAATGATTTTGGC | 10213 |
rs771957813 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358930 | CCCTTCGTATTTGAG[A/C]CTTCTGTTTCTATAA | 10213 |
rs771990416 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161334978 | TGCTTAGTGAAATTA[C/G]GGTAGTGGTCAGCAG | 10213 |
rs772046903 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324907 | TTAATAGGTCACTTT[C/T]AGGTGAAAGCTTTAA | 10213 |
rs772058957 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382299 | GTCCTCTGTTTTGAT[C/T]TGTGAGTTGCGCATA | 10213 |
rs772072395 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396206 | AATGTTACCCTAGGC[A/G]AAATAAACATCACAG | 10213 |
rs772135806 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323058 | CATACTGCCATTAAA[C/T]CTTTTCTTCTATTTA | 10213 |
rs772146373 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363704 | TGATCTGTAGCTGTG[A/T]AATGGGAAAAGTTCC | 10213 |
rs772189016 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161325056 | AAATCACATGATTTC[A/G]CACTGTGAAATTCTG | 10213 |
rs772193008 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161309135 | TAAAAACAAAGTGTG[C/T]TACTATGGCTGTTAA | 10213 |
rs772193521 | in-del | -/AT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161367166 | CCAACAGCATTTCAC[-/AT]ATACACACTGTGGTA | 10213 |
rs772233562 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313361 | ATTAATTAATTTATT[A/T]ATTTTTGAGATGGAG | 10213 |
rs772294482 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383641 | TGTTGTGATATATAA[A/T]GAAATTTTCATAATT | 10213 |
rs772310287 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161353986 | TTTTTACATGTTTTG[A/T]GATTTAAATACATAA | 10213 |
rs772315749 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310384 | AATTTTCAATTTTGT[A/G]GTAACGTTCATTTAA | 10213 |
rs772324617 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161334206 | GTGGGTATGGTGTTG[C/T]ATGCCTGTAATCCCA | 10213 |
rs772372755 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161364539 | CCCTCATATCAGCTG[C/T]TCATGTTCTTACATA | 10213 |
rs772385158 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365082 | TTGCACTCCAGCCTG[A/G]GTGACAGAGCGAGAC | 10213 |
rs772398607 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404695 | GTGATTTATTTTCTT[A/G]GTGCACTGAGTCTTG | 10213 |
rs772460256 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161408786 | GATTATCCTGCAGTG[G/T]GAATAGAGGATTTAT | 10213 |
rs772465705 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343976 | CTTGTCATTATTCCC[A/C]AAACAATATAATAGC | 10213 |
rs772528645 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161316986 | TTTGGCCTAGAATAT[A/T]TATATTCTAATGTAT | 10213 |
rs772549832 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396254 | GAAAAGGCATAGAAC[A/G]GATCCCGCAATCCCA | 10213 |
rs772550632 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372154 | ACAGAAATTGGCTAG[A/G]TGGTTACTGCTTTAA | 10213 |
rs772554212 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401964 | CTTATCTCTAAAATG[A/C]GGTTAAGGATTGTGA | 10213 |
rs772563456 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354708 | CACACATTTTTTAAA[C/T]AGGTGAAAATTGTTT | 10213 |
rs772635853 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396972 | AGCTGGGATTACAGG[C/T]GCCCGCTGCAACACC | 10213 |
rs772649309 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337781 | TAGCAGGAAGGGGAT[C/T]AGACTATGGATCAGG | 10213 |
rs772683054 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313904 | TGCATCACATAAAAT[G/T]TACTATTCTAACTTT | 10213 |
rs772702802 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161379766 | GCAAAGGAGAAAGTG[A/G]AGGTAGATTGGGTAG | 10213 |
rs772743909 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161327649 | ATTATCCCCAAAAGA[C/T]TACAGAAACAAACTT | 10213 |
rs772767664 | in-del | -/A | 0.00087489 | 0.0208969 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385430 | TATCACTTGCTTTTT[-/A]AAAAAAAATTGACTT | 10213 |
rs772797306 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161330127 | GTTCTTAGAATGGAA[A/G]GGGATTGGTGATAAA | 10213 |
rs772810628 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386998 | TTTAAAGTGCACCTT[A/C]TAAAGCAGGTTCCAA | 10213 |
rs772851179 | snp | C/T | 0.00501298 | 0.0498132 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318803 | TTAGGAACGTTTTTT[C/T]TTTGTTTCTGTTTTC | 10213 |
rs772926417 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321431 | AATGTCCAAGACATA[-/T]TTTTTTTTTATATCA | 10213 |
rs772951721 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392681 | CCACTTCCCCCTTGG[C/T]GCAAGGGGATCTTAT | 10213 |
rs772992860 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161370047 | CCCAAATAATATACA[C/T]AGGGAAGCTTTTTTT | 10213 |
rs773007341 | in-del | -/TG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313866 | GTATTTGTCATCCTG[-/TG]TGTGTGTGTGTATGT | 10213 |
rs773029567 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161373736 | AAACCACTTTCTTGA[A/G]CATTTTGTATATTTC | 10213 |
rs773060661 | in-del | -/ACTG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336818 | GGCCTCAGGTGATCC[-/ACTG]ACTGCCTCAGCCATC | 10213 |
rs773081671 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377907 | CATTGGAATTATAGA[A/G]AAGAATACGATCTAC | 10213 |
rs773099582 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161362113 | ACTCTGTTGCCCAGG[A/C]TGGAGTGCAGTGGTT | 10213 |
rs773148317 | in-del | -/GTGCCAAGA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377880 | GTTGATCACTACTTT[-/GTGCCAAGA]GTACATTGGAATTAT | 10213 |
rs773169446 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359902 | CTTGTGATATATGTC[A/G]ATGTAGATGTATATT | 10213 |
rs773184685 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345617 | TTATCACTGATTTTG[A/G]GTTATGATATTCATT | 10213 |
rs773218665 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400979 | AATTTGTCAAAATGT[A/G]TACATACATAGATGT | 10213 |
rs773274598 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396217 | AGGCAAAATAAACAT[A/C]ACAGGCAAGGGCTAG | 10213 |
rs773277525 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393392 | TTCCTAATTTTTTTT[A/G]GCATACTGTCCTTAC | 10213 |
rs773278814 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382493 | AAGTAAGAGGTTTCC[C/G]TAAGCTAGCCAAACT | 10213 |
rs773305216 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161309261 | CTTGCAACTTAATTT[C/T]CCTGGGGATGTAGCT | 10213 |
rs773328255 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398693 | ATTTGGAGATCTGAC[A/G]GTTTACTGTTCAGGT | 10213 |
rs773345595 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161370803 | CTGGTGTCCATTGTT[-/A]AAAATGTACTCTGTG | 10213 |
rs773348839 | snp | C/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307357 | AGAGGCAAGTGTTCA[C/T]ACTCTTAAGTTTCTG | 10213 |
rs773356756 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310429 | CCTGTGAAAGCCTTG[C/T]CTGAATATCCATGTG | 10213 |
rs773362475 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161363754 | ATTCGATTGGGATGT[A/G]GCCTGCTTCTTCAGT | 10213 |
rs773409398 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403678 | TATTTCTTATCACTG[C/T]TGTGTTGTTGAAATA | 10213 |
rs773532769 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311867 | TGATCCAACCGCCTC[A/G]GCCTCCCAAAGAGCT | 10213 |
rs773566827 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354102 | ACAATTCTGATACCT[C/G]AGTGTTCTGTTATGA | 10213 |
rs773585969 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313384 | AGATGGAGTCTTGCT[C/G]TGTCGCCCAGGCTGG | 10213 |
rs773603023 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331644 | GAAAATTGTAGTAAT[A/G]TAGGGAGACAGTCAG | 10213 |
rs773609874 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396260 | GCATAGAACAGATCC[C/T]GCAATCCCACCACTG | 10213 |
rs773653620 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372295 | ATAATTTTTAGAGTA[C/T]TTAGAAATAAATATT | 10213 |
rs773737955 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343965 | GTACACTTTTTCTTG[C/T]CATTATTCCCAAAAC | 10213 |
rs773815958 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161409644 | TGGATGGGAAATCTC[-/T]TAAGAATCACCCAGC | 10213 |
rs773915423 | snp | C/T | 1.88514e-05 | 0.00307007 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318921 | GTGTAAACTACAAGC[C/T]TTTTTGTAGTTAGCC | 10213 |
rs773981006 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392031 | TTTTCAAGTTTGATT[A/G]GTTTTTAACATTACC | 10213 |
rs774005232 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386722 | CTTTCTTATAAACTT[C/T]GGTAGCATCATACTG | 10213 |
rs774039866 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345345 | TCTCCTGGGCTCAAG[C/T]GATCCTCCCACCTCA | 10213 |
rs774045439 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161384239 | ACAGAAGCTTAGACT[A/G]ATTAACTTGTCATCA | 10213 |
rs774047633 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400930 | TTTTATCATTTGCTA[C/G]CATAAAACATACACT | 10213 |
rs774093723 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161402219 | ATTTTCCATTCTGTA[A/G]AATGATCTTTCTAAA | 10213 |
rs774095083 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161327506 | AACTAGTCAGGTGCA[C/T]AGCAGATACCCTTCC | 10213 |
rs774095204 | in-del | -/TTTTTTTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161356047 | CTGTCAGCCAAAGGA[-/TTTTTTTT]TGGAACATTTTTTTT | 10213 |
rs774096001 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161370001 | GGTATCAAATGTAGG[-/T]TATCAAAACCTATAA | 10213 |
rs774137584 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386670 | TTGCATGTTCCAAGA[A/G]AATATATTATTGGAC | 10213 |
rs774181706 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161374595 | ATCAGTGAAATAGTT[G/T]ATAAGGTCCGCTTGC | 10213 |
rs774189140 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404638 | ATGACAGAGTATGGC[A/G]CTGATGACAATTTGC | 10213 |
rs774238954 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321336 | TTTCCTTGATTGAAG[A/G]ACAAGAACCATGGAC | 10213 |
rs774253875 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392703 | GGATCTTATAATGCT[C/G]TCTTCTAATTGCCTG | 10213 |
rs774258894 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378128 | TGTCATTGTAATTTT[C/G]TAAAGAGGGTAAAAA | 10213 |
rs774269657 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357844 | TCTAATAGGTATTAT[C/T]AAATGACCTTGAAGT | 10213 |
rs774269791 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375793 | TCCCAGCACTTTGGG[A/C]GGTCAAAGTGAGTGG | 10213 |
rs774290713 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318560 | CTTAATGATAGCAAA[C/G]TTTTGAAAGTATGCT | 10213 |
rs774443766 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321930 | GTTTTTATTGGGACT[C/T]GGCATACATGAGCTT | 10213 |
rs774450225 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396190 | CTTGAACATACAAAG[A/G]AATGTTACCCTAGGC | 10213 |
rs774500363 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322818 | TTTATTTGGGAGTTG[C/T]AGTAGGGCTAGTAGG | 10213 |
rs774543540 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161379582 | GGTAACTTTTTTCCA[A/G]TTTTAACACTCTTCA | 10213 |
rs774572373 | snp | A/G | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161308094 | TTTGAGGAGGGCAAT[A/G]ATAGTAGTGAACACC | 10213 |
rs774584975 | snp | A/C | 2.49622e-05 | 0.00353277 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408935 | GTTATGCAGTTGCAT[A/C]ATAACATGTTCTTAT | 10213 |
rs774603415 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161369867 | ACATATACACAGCAA[C/T]GGCCATATACTCTTA | 10213 |
rs774691174 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161353608 | GTATTCCCTAATTCT[C/T]AGCATAAAGGAAGAT | 10213 |
rs774696886 | snp | A/G | 5.52532e-05 | 0.00525581 | missense | PSMD14 | GRCh38.p7 | 2:161411389 | ATGTTGGATACTGTC[A/G]TATTTAAATAAAGCA | 10213 |
rs774711359 | snp | A/G | | | missense | PSMD14 | GRCh38.p7 | 2:161367854 | GAGAATTTGTTGATG[A/G]TTATACCGTCAGAGT | 10213 |
rs774714212 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161362016 | TGTCAGTATTGTGTT[C/T]GGTTTTTCTTCCCCA | 10213 |
rs774724549 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161340899 | AGCTTCCCGGGGCTG[C/T]ATTTGAAGGAGAAGC | 10213 |
rs774765826 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161407585 | TACAAAACTATTAAG[A/C]AGGTGTGAAATGCAG | 10213 |
rs774788565 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396035 | CTCTTGTAGTTAGAC[A/G]TTAGAGAAACACTAC | 10213 |
rs774803199 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352104 | ATTGGCTCAAGACCT[A/C]TGAAATTCCTAGACA | 10213 |
rs774881699 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318487 | ATATGATAAGCATTT[C/G]AGGCACTTTTTCTAC | 10213 |
rs774887750 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357750 | TGTGTGTGCTTATTT[C/T]ATAGTGGCATTGTAT | 10213 |
rs774903717 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397362 | CACTGGTCGGATAGA[C/T]GAAGTGAAAGAAGGA | 10213 |
rs774908223 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386285 | TAGTTAATTACTACT[A/C]TAAAGATTAATTAAA | 10213 |
rs774971591 | in-del | -/GT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324600 | ACTTTTTTCCCCTAG[-/GT]GTGTTGTAGTTTCAT | 10213 |
rs774998231 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342624 | TTGTGTTTTGCTTTT[C/T]TTTTTTAAAATCCAG | 10213 |
rs775090397 | snp | A/C | | | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411409 | TAAATAAAGCAACGA[A/C]AAACGCTATTAATGA | 10213 |
rs775100046 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161403574 | GTTCATGTCACTACC[A/G]TGCTTTTAAAAAGCC | 10213 |
rs775100996 | snp | C/T | 1.67142e-05 | 0.00289081 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370192 | GGTAAGCATTTTAAA[C/T]GATCAGTTAAAGAAA | 10213 |
rs775154877 | snp | A/G | | | downstream-variant-500B | PSMD14 | GRCh38.p7 | 2:161411800 | CTCACACAAAGATAT[A/G]TTTCCGTTTGCATTT | 10213 |
rs775175534 | in-del | -/CGCCTCCCAGGTTCAAGCGGTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331347 | GCTCAGTGCAACCTC[-/CGCCTCCCAGGTTCAAGCGGTT]CGCCTCCCAGGTTCA | 10213 |
rs775188872 | snp | C/T | 1.68792e-05 | 0.00290505 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161367810 | TGGCCGTGCTGGAGT[C/T]CCAATGGAAGTTATG | 10213 |
rs775193791 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161399095 | AAAAATATTCAGGAA[G/T]TAACCATCACAAGAA | 10213 |
rs775255168 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343907 | CTTATCCATGGGTTC[C/T]GCATCCATGGATTCA | 10213 |
rs775306170 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389777 | ATAGTATGTTAGAAA[G/T]AACATAGGCTATGGA | 10213 |
rs775351706 | in-del | -/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347380 | TCTCGAACTACTCAA[-/G]GAATCCTCCTGCTCC | 10213 |
rs775373305 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346905 | CCTCACACACATGCA[G/T]TGATCATTATTAAGC | 10213 |
rs775410376 | in-del | -/AT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161376108 | TGTATATATATACAT[-/AT]ATATATATATATACT | 10213 |
rs775418766 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161317484 | AGACTGGAAGCGGGG[C/T]TTGGGTGGCGTTTCT | 10213 |
rs775488378 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372774 | TTTAGTAACTCGTAA[C/G]TAATTCATTTAAGTA | 10213 |
rs775494153 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161351868 | ATTGGCTGAAGAGGG[A/T]CACATGTTCATACCT | 10213 |
rs775543380 | in-del | -/A | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324462 | GCTGAGTTTTGAAAT[-/A]ATGTGTCAAGGCATA | 10213 |
rs775581102 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335427 | ATGTTTAAATTCTGT[A/T]TAATTTAAAATAGTT | 10213 |
rs775609876 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321626 | CCACACTTTGGACTG[A/G]CACTTTAACCTGAGT | 10213 |
rs775717843 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392897 | ATCTGACACCCATCT[A/T]TTTGGAAATGTCTAG | 10213 |
rs775720562 | snp | A/T | 2.21256e-05 | 0.00332601 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385439 | CTTTTTAAAAAAAAA[A/T]TGACTTGACACCTTG | 10213 |
rs775764545 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320018 | ATAACTCATTCTCTC[A/G]AGAGGCCTAAGCCTC | 10213 |
rs775840691 | snp | A/G | 1.65586e-05 | 0.00287733 | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411407 | TTTAAATAAAGCAAC[A/G]AAAAACGCTATTAAT | 10213 |
rs775854597 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161384100 | AAGTTTTCACAAACT[A/G]TTAATTCATGTTCTG | 10213 |
rs775873141 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406261 | AATTCCAAGGATTTC[C/T]TAGAGCTGTGCAGAC | 10213 |
rs775974556 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161367395 | CTATTTTAAAAATAT[C/G]AAGTTTATACCACAT | 10213 |
rs775976561 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161350610 | GTGTCTTGATTAATC[A/G]AAGTAGCAGGAAGGA | 10213 |
rs776078379 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312389 | CCTCAAGTGATCTGC[C/T]CCCCTCGGCCTCCCA | 10213 |
rs776134643 | snp | A/G | 2.10188e-05 | 0.00324175 | intron-variant | PSMD14 | GRCh38.p7 | 2:161411257 | AGTAATTTATCTACC[A/G]GTAATATGGTTCTGT | 10213 |
rs776139663 | in-del | -/AA | 2.05675e-05 | 0.00320676 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385598 | ATTTGATAATGTGTT[-/AA]AACTCTTTTAAATTT | 10213 |
rs776146049 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161331742 | ATATTTTGAAATGTG[C/T]ATTAAAATTTTCCTC | 10213 |
rs776227347 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359980 | AAGTGGTAGCACATG[A/T]TGAATACTTAAGTAT | 10213 |
rs776291188 | snp | A/T | 2.25466e-05 | 0.0033575 | utr-variant-3-prime | PSMD14 | GRCh38.p7 | 2:161411420 | ACGAAAAACGCTATT[A/T]ATGATGCCTTCAGTG | 10213 |
rs776299028 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345834 | GCTTTATTTTTTTCC[C/G]CAATCATTTTGCCCT | 10213 |
rs776384468 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357786 | ACGAGACTATTTTAT[A/G]TAGCTTAAGTACCTC | 10213 |
rs776388544 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354924 | TATTCTCAAAATACT[A/G]GCTGTAGGGCCACCA | 10213 |
rs776476199 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338264 | AAGTTCTGAAACTGC[A/G]TTTGTGTGTGCACAT | 10213 |
rs776476315 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357543 | ATTGAGGATTTATAT[A/G]GCAAAAGTAATTATT | 10213 |
rs776485665 | snp | C/T | 1.72024e-05 | 0.00293273 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370224 | AATGGGAAATATTTA[C/T]AGAAACATACCTCAA | 10213 |
rs776504420 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161379409 | TTCAGTCATTTTTAA[A/G]AGAGAGATAATAACC | 10213 |
rs776506841 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380689 | TTGAGACTAAGAAAT[A/C]ACAGCAATTCAGTGA | 10213 |
rs776569551 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161362159 | CAGCCTCAGCCTTTC[A/G]GGTTCAAGCCATCTT | 10213 |
rs776573645 | snp | C/G | 2.6546e-05 | 0.00364311 | missense | PSMD14 | GRCh38.p7 | 2:161395138 | CTTCAGGACTACAGT[C/G]AACATTGTAAACACA | 10213 |
rs776595526 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161330723 | GCCTCTCAGTGCTGC[C/T]TTTTAAGCTGTTGCC | 10213 |
rs776616977 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161388764 | TGAAAACTTTTAAAA[A/G]CTTATCAGGAACCCA | 10213 |
rs776630267 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365371 | ATCAGTACTTATTAA[A/G]TTCTTACTATGGCCC | 10213 |
rs776651881 | in-del | -/AAA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161343828 | GTGATACTCTGTCTC[-/AAA]AAAAAAAAAAAATGT | 10213 |
rs776739378 | in-del | -/CTTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346743 | CTATTGAGGCTAGAC[-/CTTT]CTGTCTCTTCTAATT | 10213 |
rs776761667 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335264 | CCAGTTTCTTTATGT[C/T]CTTCCAAAGATAATT | 10213 |
rs776798917 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404851 | TCTGCTGCCTTTGCT[A/G]TGAGCATTTCCAAGA | 10213 |
rs776821702 | in-del | -/GT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365434 | ATATTGAAGAAAATA[-/GT]GTTTCTTCCTTCTTT | 10213 |
rs776861109 | snp | A/G | 0.000432994 | 0.0147075 | intron-variant | PSMD14 | GRCh38.p7 | 2:161391203 | AATTTTTATCTTATA[A/G]GAGGAAAAAAATCTT | 10213 |
rs776902207 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333500 | GAAAGGCAGTATATA[C/T]TGGGCAGTGGTAAAA | 10213 |
rs777010327 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397120 | CAGGAATGAGCCACC[A/G]TGCCTGGCCTAAGAG | 10213 |
rs777043770 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310673 | ATAAATTGCTTTGGA[C/T]GTATTTTTACAACAG | 10213 |
rs777049413 | snp | C/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161307871 | GTAAACTAAACTCGG[C/T]TTAAAATAGGTGGTT | 10213 |
rs777118933 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383879 | TAGTATGAGTGTGAG[A/G]AAATTTTACTTCTAT | 10213 |
rs777171129 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342456 | CCTTGTAACAATTCT[G/T]TGCTCTGAAATTGGT | 10213 |
rs777251149 | snp | A/C/T | 0.000115905 | 0.00761193 | intron-variant | PSMD14 | GRCh38.p7 | 2:161318795 | TTTTGTGCTTAGGAA[A/C/T]GTTTTTTCTTTGTTT | 10213 |
rs777299052 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346523 | TTTTTTTGCTGCTTT[C/G]TATGTCTGATAGTTT | 10213 |
rs777299684 | in-del | -/CTTC | 9.42036e-05 | 0.00686243 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367770 | TTTGTGTCCACATCT[-/CTTC]CTTTCTACAGATGTT | 10213 |
rs777352428 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347327 | CTTTTATTTATTTAT[C/T]TTTTGGGAGAGGAGG | 10213 |
rs777380728 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342984 | ATACTCCATATATGC[C/T]CTCTGGACCTTTGTG | 10213 |
rs777382894 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310208 | GTTCATCTTATTTTC[A/G]TACTGGCCATGTAAA | 10213 |
rs777398879 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161308763 | TTCTCTTCGCCTGCT[C/G]TCAGGGCTCTCTGGC | 10213 |
rs777437944 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354435 | AGTTTTTTGTAGAGA[C/T]GGTTTCGTCATGTTG | 10213 |
rs777479035 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378513 | TTTTTTGAGGTTTTC[A/G]TTTCAATAGATATTT | 10213 |
rs777486070 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397010 | TTTTTATATCTTTTA[A/G]TAGAGACGGGGTTTC | 10213 |
rs777488009 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357695 | CTGTGAAGTTGCAGA[A/G]TATTCAGATGTTTCT | 10213 |
rs777526928 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161309833 | TTGTTTTTTTTTCAG[C/G]CTAAAGTGCTTGGTA | 10213 |
rs777541605 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161410451 | CATTTAAATTATAAT[G/T]TTTCTATTGTGTATA | 10213 |
rs777565932 | snp | C/T | 2.62326e-05 | 0.00362155 | intron-variant | PSMD14 | GRCh38.p7 | 2:161408817 | AATTTTAAACTCTGT[C/T]CTTTGTGTTTCATTC | 10213 |
rs777641319 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394219 | TCAACTGATTCACCC[C/T]CCTTGGCCTCCCAAA | 10213 |
rs777643259 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161408523 | GTAAGTGCCACCTCA[A/G]GTACTTCCATCTCCC | 10213 |
rs777651165 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336599 | CATTTATTTTGAGAC[A/G]GAATCTTGCTCTGTT | 10213 |
rs777657675 | snp | G/T | 0.000225606 | 0.0106185 | intron-variant | PSMD14 | GRCh38.p7 | 2:161395071 | TACTTTTTCTTTTAT[G/T]TTTTAGATGTTGCTA | 10213 |
rs777731532 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395613 | TGTCTAATTTATTTT[A/G]TGAACGTTTCCATTA | 10213 |
rs777758651 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398601 | GTGCAGGTGAAAAAA[C/T]GAATTGTGAAGAACA | 10213 |
rs777792725 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321406 | ACGAATAACCCAATT[C/T]TGATGAACGAAATGT | 10213 |
rs777820988 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161380854 | GCAGTGCATGGCAGC[A/G]GAAGTAACGAAATGG | 10213 |
rs777862790 | snp | A/C | 1.69367e-05 | 0.00290999 | missense | PSMD14 | GRCh38.p7 | 2:161411324 | AACGTCATTTGGAGG[A/C]ACATGTGGATGTACT | 10213 |
rs777921366 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322553 | AGCCTCCACGCCCAG[C/T]TAATTTTTTTATTTT | 10213 |
rs777936729 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161385339 | TTTTTTATTAATATT[A/G]TAATTAAATGATTTT | 10213 |
rs777980000 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161316998 | TATATATATTCTAAT[A/G]TATACTGTATGTTGT | 10213 |
rs778016019 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161384023 | AGTATAAGCATGTAG[A/G]CCATATTTATATATA | 10213 |
rs778069487 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161316197 | TTTTGAAATGTCTGT[C/T]TTCAAAGTTAGTGTT | 10213 |
rs778114167 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366877 | GTGGTTAGGATTTTG[G/T]AAGTATTTTCACGTC | 10213 |
rs778118088 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161327062 | AAATTCTGACATATG[C/T]TACAACATGAGTGAA | 10213 |
rs778170181 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368211 | GCAGAGTGTTAGTTT[G/T]ATTTTGAACCAAGTG | 10213 |
rs778226513 | snp | C/T | 7.99584e-05 | 0.00632241 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370089 | AAAATTAATAATTTT[C/T]CTTTCTTTCTAAATC | 10213 |
rs778230044 | snp | C/T | 3.32209e-05 | 0.00407546 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370104 | TCTTTCTTTCTAAAT[C/T]AGGGTGTCAGTGTGG | 10213 |
rs778273487 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161319552 | CTGTGCAGTCATACA[-/T]TGAGTTAATACTAAT | 10213 |
rs778275296 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318094 | ATTGATATAGTAAAT[A/C]CACTTTGTATTGGTT | 10213 |
rs778335576 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377301 | AAAGAAATCTATTTC[C/G]ATTCCTGACATAGCT | 10213 |
rs778396798 | snp | G/T | 3.9729e-05 | 0.00445679 | intron-variant | PSMD14 | GRCh38.p7 | 2:161367756 | TCAACGAAATTTGCT[G/T]TGTGTCCACATCTCT | 10213 |
rs778400501 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357470 | CTTTTTATAACAAAC[G/T]TATTTTCAAGAGTCA | 10213 |
rs778422679 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161309986 | TAACATAGTGAAAAC[A/C]CGTCTCTACTAAAAG | 10213 |
rs778425603 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161378917 | ATACACAGCAAAGTA[A/G]TTGGCCTTTACATAT | 10213 |
rs778426687 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394944 | AGGAGCATTCTAATT[A/G]GAGTTCATTTGAATT | 10213 |
rs778444794 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161308676 | GCCAGCCCCGTGCTT[C/T]CCTGAGTCACGTTGC | 10213 |
rs778471442 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346393 | TTTATGTTTTCCATG[A/T]GTCTCCTTAACTTTT | 10213 |
rs778513579 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360815 | TGCTAGGATTACAGG[C/T]GTGAGCCACCACGCC | 10213 |
rs778528886 | in-del | -/T | 7.14124e-05 | 0.00597504 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385424 | GGCATTATCACTTGC[-/T]TTTTTAAAAAAAAAT | 10213 |
rs778547918 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161321098 | CATTAGATAAGGCAT[A/G]GGCACCAATAGTAGT | 10213 |
rs778557076 | in-del | -/ACACAGCTAAAGTGGTA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359956 | AGCTTTTGTTTAACC[-/ACACAGCTAAAGTGGTA]GCACATGATGAATAC | 10213 |
rs778562719 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338670 | TGAGATATAATTGAC[A/C]TACAGTAAACGATAA | 10213 |
rs778620522 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406975 | TGTTTGCAATATTCC[A/G]CAATACTCCCTAATA | 10213 |
rs778631832 | in-del | -/TGTGTGGT/TGTGTGTGTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161327986 | GTGTGTGTGTGTGAG[-/TGTGTGGT/TGTGTGTGTT]ATGTTGGTTAGGAAT | 10213 |
rs778663593 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352760 | TTCTTTCATTAGATG[A/C]GGTAAATAACATTTG | 10213 |
rs778697282 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401682 | CTTTATTATTCATCT[C/G]TATTTCATGTAATTA | 10213 |
rs778750765 | snp | A/G | | | | | GRCh38.p7 | 2:161326859 | TACTTATAATGCTTA[A/G]TACAGTGTAAATGCT | 10213 |
rs778926608 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161410372 | CAAGAAATAATTCCA[A/G]TAATGAACATTTGTT | 10213 |
rs778956461 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394413 | ACAAGCCCCTTAATT[C/G]ATAGATCTCTAAACT | 10213 |
rs778965025 | snp | A/G | 0.000147135 | 0.00857587 | missense | PSMD14 | GRCh38.p7 | 2:161395102 | AATTTGCATAAGAAG[A/G]GTTGGATGGAAGGTT | 10213 |
rs778994217 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337747 | CAGGTACATTTGCAG[C/T]AATTGAGATGATGTG | 10213 |
rs778998743 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161381784 | GCATGCTTGGAATAA[A/G]TACGGAACTCAGTAT | 10213 |
rs779049302 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339374 | TGGTTTTAATTTGCA[C/T]TTTCTGGATGACTGA | 10213 |
rs779062992 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336453 | ATATTATGAGTTTGG[A/G]TATCAATTTTTTCTT | 10213 |
rs779155239 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161409824 | CAGTTTAAAAACAAG[C/T]ACCCTCAAAAAGCAA | 10213 |
rs779168545 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161329768 | CCTAATCATTCTATT[C/T]ATATACTCTGATATT | 10213 |
rs779174514 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324764 | GGGAAGAGATTAAAG[A/G]CAAAGTCATCAATTA | 10213 |
rs779176012 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161329821 | GGGGTCAGGTCAAAA[A/G]CAAGCTAATTAGAGC | 10213 |
rs779274362 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347252 | GCTTTAGGTGGGAAT[G/T]TAGATTTAGTTTCTG | 10213 |
rs779315917 | in-del | -/GATAT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161374056 | TAGCAGCAGAACAAA[-/GATAT]GAATCCAGTTCTGTA | 10213 |
rs779394896 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161398324 | TTTTAAGCTAAGGTA[A/G]TTGCTGTTGGATGCC | 10213 |
rs779444387 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389330 | TCTCTACGCCAGACT[A/G]TGTCTGCTTAGAGGA | 10213 |
rs779446552 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371881 | AAACAGATTAACTTG[C/T]AAAGCATATTGGGTT | 10213 |
rs779474087 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392615 | ATCCACTCATAAACT[A/C]ATCTGAAGGGCCCAG | 10213 |
rs779480643 | snp | A/G | 2.28376e-05 | 0.00337909 | intron-variant | PSMD14 | GRCh38.p7 | 2:161385609 | TGTTAAAACTCTTTT[A/G]AATTTTAAAAGCCTG | 10213 |
rs779499335 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314798 | TAGAATTTGTTTATC[C/T]ATTCATTTTTTGGTG | 10213 |
rs779500101 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161315894 | TGTTGCCCAGGCTGG[A/C]GTGCAATGGCGCGTT | 10213 |
rs779538072 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347050 | CTGTCATCTCAACTC[A/G]GAGAGTCTACTGTCC | 10213 |
rs779553051 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406655 | TCTTAGAATTGAAGA[G/T]ATATGCTTACTCTTT | 10213 |
rs779566381 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161393931 | TGATCACTGATATAG[A/T]ATCCAACCCCAATTT | 10213 |
rs779570511 | snp | C/G | 2.61086e-05 | 0.00361298 | intron-variant | PSMD14 | GRCh38.p7 | 2:161371335 | AAGGTAGAGTAGATT[C/G]TATCTTTATTGCCAT | 10213 |
rs779631397 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161320951 | TGCTGGTCTTGAACT[C/T]CTGACCTCAAGTGAT | 10213 |
rs779633079 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161359544 | CATATTTTAATTTTC[A/G]TATTAGTATCTATAC | 10213 |
rs779639006 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161334261 | GAATCACTTTAACCC[A/G]GGAGGTGGAGGTTGT | 10213 |
rs779650680 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161377184 | GATCAGTATCCCACG[A/G]CTATCAGCTAGGGCT | 10213 |
rs779692512 | in-del | -/TG | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313865 | TTGTATTTGTCATCC[-/TG]TGTGTGTGTGTATGT | 10213 |
rs779700236 | in-del | -/TGCACCACC | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161370321 | TAAATATCAGTGCCA[-/TGCACCACC]TGTCTAGTATATCTT | 10213 |
rs779802067 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326196 | CCACCACGCCCGGCT[A/G]ATTTTTGTAGTTTTA | 10213 |
rs779819659 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311399 | GTATAACTATTTGTA[C/T]TGTATTTAATTGTAT | 10213 |
rs779823929 | snp | C/T | 1.78825e-05 | 0.00299014 | intron-variant | PSMD14 | GRCh38.p7 | 2:161411296 | TCCTCATTTTTGTTC[C/T]TTTAGGACCCCAAAC | 10213 |
rs779841849 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383606 | CAAAGCATTCAGTAT[A/C]AAAAAGTATATAGGA | 10213 |
rs779844359 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161405295 | CTGACTCTCCCTCTG[C/T]TTCCCCAGGTGATCC | 10213 |
rs779878695 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310279 | GAAAGTCAATAAATA[C/T]TATTGCTGTTGTTAT | 10213 |
rs779895235 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333191 | TGTCTTTCCTTACTG[C/T]TCCATATCTTCATTG | 10213 |
rs779941719 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404533 | TGCCCCTCTCCCTTC[C/T]TTGAGGCTAACTGGA | 10213 |
rs779944318 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389226 | GCTACAGCAGTTACT[A/G]GCTTTATGACCACCA | 10213 |
rs779979626 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161350556 | ACAGATAAAATGTTA[C/T]TATAGTTGTGTTGAC | 10213 |
rs780027096 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161365021 | GAGACAGGAAGAGAC[G/T]CTGGAACCCAGGAGG | 10213 |
rs780030073 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161371496 | GTCTTGGTATTATTA[A/G]CAATTTATTTAGAGA | 10213 |
rs780096375 | snp | A/G | 8.23215e-05 | 0.00641513 | synonymous-codon | PSMD14 | GRCh38.p7 | 2:161408863 | AGAAGATAAGATGAC[A/G]CCTGAACAGCTGGCA | 10213 |
rs780125843 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349380 | AGGCATCAGAATGCC[C/T]GCTTGGCATGTTTGT | 10213 |
rs780140926 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161353451 | CTAATTAGGAATCCA[C/T]GCTTTAGTTAGCTCA | 10213 |
rs780175768 | in-del | -/TT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339498 | ATTTTGTTAATGAAT[-/TT]TTTTTTTTTTTTTTT | 10213 |
rs780223958 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323621 | TGAGCCAAGGTAGTA[C/T]CACTGCACTCCAGCC | 10213 |
rs780235567 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354482 | ATGTTTTTTTATAAC[A/G]AAGGTAGTCGAGCAT | 10213 |
rs780284532 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326500 | AAAACATTATTATTC[C/G]TTAAATGATTAAACA | 10213 |
rs780293137 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161337643 | TAACCAGTGCAGAAA[C/T]GATTGTTCTTAGTTT | 10213 |
rs780312354 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161345035 | CTTATATTGAGTTCC[A/G]TGATCCATTTTGTAC | 10213 |
rs780351180 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161362629 | AAAATTGAGTATAAA[A/G]TTCTTTACTTTCAGT | 10213 |
rs780370505 | snp | C/T | | | upstream-variant-2KB | PSMD14 | GRCh38.p7 | 2:161306287 | TATGAATGAATTCTT[C/T]AAAGTCTGCATTGTT | 10213 |
rs780385658 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161316018 | GGCTAATTTTTTTGT[A/G]TTTTTAGTAGACACA | 10213 |
rs780424220 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406614 | TGGGTAGATAGAGAA[A/G]ATATTTAGGCATTTG | 10213 |
rs780472367 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161360624 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG | 10213 |
rs780519329 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161395683 | ATCATACATGTATAC[A/G]TATAGATTGCAACTC | 10213 |
rs780526528 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400331 | TGGGTTTCATGCAAC[A/G]GGAAGAGAAGAAAGG | 10213 |
rs780552134 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161346319 | ACTCACCCCCTGCTT[C/T]ATCCTATTGCTAGTG | 10213 |
rs780613873 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404202 | TTGTGAGCCACTATG[C/T]CCAGCCTAATTATTA | 10213 |
rs780665761 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161397408 | GAATTCAAAGTTTCC[C/T]GCCTGGGTGACCAGT | 10213 |
rs780704937 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161392555 | GAAATAAGAATTCTA[A/G]TTTTGTTTTTTTAAG | 10213 |
rs780783034 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161349053 | GAAGACAGATCAGCT[G/T]TCTAGGTAAATGACC | 10213 |
rs780827532 | in-del | -/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161312472 | TTTTAAATCCAGCAT[-/G]GACATGATCTAGCAA | 10213 |
rs780836131 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161332859 | GTAATTTTGGTTGGG[G/T]ATCTGACTGGCACAG | 10213 |
rs780862862 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161374004 | AAAAAAAAAATTAGG[A/G]CCAATGAGATTGCTT | 10213 |
rs780885582 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161318449 | TGTACACTCTGGACC[A/T]ATTGAAGGAAATTCA | 10213 |
rs780923593 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161324497 | AAAGGCTAGAGAATA[G/T]ATACATAAGAAAATA | 10213 |
rs780975350 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396849 | TGTTTGCTTTTTGAG[A/T]TGGAATCTCACTCTG | 10213 |
rs780987673 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161339110 | TGTAAACATTATGTA[C/T]ATGACATTGTATGGA | 10213 |
rs781046327 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161310107 | AGTGAGCCAAGATCG[C/T]GCAACTGCACTCCAG | 10213 |
rs781074742 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161401338 | AGTCAAAGTGACATA[C/G]AGATTTTCACCTGTG | 10213 |
rs781116526 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161385403 | CATGCCTTGTCCACT[C/G]TTGCTTGGCATTATC | 10213 |
rs781181595 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161404010 | TCCTGAGTTTAAGCA[C/G]TACTCTTGCCTCAGC | 10213 |
rs781190548 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161386206 | GGTGTTTTTATACAA[A/G]TCTTTATTTTCTGCA | 10213 |
rs781248487 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383334 | CAAATTCCTTTAATC[G/T]TAGTGTAAAGTAGTC | 10213 |
rs781252693 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161333230 | TATATTTTATAGGAA[A/G]TTTCCTTTTTTAGTA | 10213 |
rs781278720 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161367334 | TGCAAATGTGTTTTG[A/G]TTATGTCATAGCCAA | 10213 |
rs781278792 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161387670 | TGCAAGTGTATATTT[C/T]ATAGATGGTGCCTAT | 10213 |
rs781290487 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161352678 | GCCCACATTCACCCA[-/T]TTTTTTTGGATTCCC | 10213 |
rs781347145 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366922 | CAACTGGTTTGTTCA[C/T]ACCTGGGGCAATTGT | 10213 |
rs781355918 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161375476 | CAAGGGAGAAATCAG[C/T]TGTAGGTTGCACAAA | 10213 |
rs781434889 | in-del | -/CTT | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383083 | TGGCATAATTAACAC[-/CTT]CTTCACCCATTGCTC | 10213 |
rs781446805 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161350055 | AAAGTATGCTTATTT[A/G]AAGACAAATACGTGG | 10213 |
rs781449646 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161357839 | TTTATTCTAATAGGT[A/G]TTATTAAATGACCTT | 10213 |
rs781515400 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161368625 | AAAAAAAGCACATAT[A/G]TCCTTCTCACCTGTT | 10213 |
rs781530590 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161314241 | AAACATCAAAAAATA[C/T]GTGACACATCTCTTT | 10213 |
rs781538946 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161353179 | AGTGAAATCTTGGGT[A/C]CTTAAGACTTAATAT | 10213 |
rs781548684 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161407171 | GTCAATAAAGTTTAG[A/T]GTCACAATTTGTGAA | 10213 |
rs781562903 | snp | A/G | 3.41344e-05 | 0.0041311 | intron-variant | PSMD14 | GRCh38.p7 | 2:161370081 | AATTTACAAAAATTA[A/G]TAATTTTTCTTTCTT | 10213 |
rs781606576 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161338804 | CCCCAGTGTAGTCCC[C/T]TTCCTTGCACTTCTC | 10213 |
rs781674139 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161336938 | CATTTTAAGTTTTCC[G/T]TGACTTCATTTTTTA | 10213 |
rs781698239 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161406009 | CAACAACAACAAAAA[A/C]AACAAAAAATCCATT | 10213 |
rs781717029 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161358666 | TTTAAAGAGCCTGGC[C/T]GGGCACGGTGGCTCA | 10213 |
rs781719438 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161400187 | ATATTTCAAGTCCAA[C/T]ATAAAACTTCAAAGA | 10213 |
rs781730779 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161372886 | TTTAAATATAATTAG[A/G]ATTCTATTTTGTAGT | 10213 |
rs781741072 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326431 | GTGAGGATTGGAGAA[A/C]TTAGAACTCTTGTAC | 10213 |
rs781773867 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161344926 | TCTTCTCTTTTTTGA[C/G]TTCTGCTTTTGATAT | 10213 |
rs796065377 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382805 | AACTAATTTAATGTC[C/T]ATATACTTCAAAATG | 10213 |
rs796070501 | multinucleotide-polymorphism | AG/CA | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161334992 | GGGTAGTGGTCAGCA[AG/CA]ATTTCTAGGAAGCCT | 10213 |
rs796083704 | in-del | -/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161313025 | AGCATTGTGTTAAAT[-/G]TTTTTTTTTGTGTCC | 10213 |
rs796090877 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161383029 | GCTTATACACACCAT[C/T]GAGTGCTCACTAGGG | 10213 |
rs796211471 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161322016 | CCCAAATGGGCCTGG[C/T]TCAAAGTCTTAGCCC | 10213 |
rs796243217 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161382678 | GCATCATATTCCTGA[A/G]AATATTCTTCATACT | 10213 |
rs796322123 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161348638 | GTACAATTTTAAGAT[A/G]CCCAAAATGATACTG | 10213 |
rs796342373 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161361483 | TCACATACATATTAT[C/T]GGAAAATAGAAAATG | 10213 |
rs796376561 | in-del | -/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161389889 | TCTTTCTTTTTTGTT[-/G]TTTTTTTTTTTTTTT | 10213 |
rs796390537 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161381586 | GATTGGTGCTTTACA[A/G]ATTTAGTCTAGTCTT | 10213 |
rs796397852 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161396640 | GAGGTTTGGGTGGAG[C/T]GGGGTGGGTTGGGAA | 10213 |
rs796407013 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161326548 | CCAGCAATTCAGCTT[C/T]TGGGTATGTGCCCAA | 10213 |
rs796431156 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161381450 | AAAAGAGAGAGAGAA[A/G]AAAATTACAGCTACT | 10213 |
rs796432612 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161323627 | AAGGTAGTACCACTG[C/T]ACTCCAGCCTGGGTG | 10213 |
rs796451931 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161387852 | TGTTGAAATAAGCTA[A/T]GAGACAAAGGTTATT | 10213 |
rs796462949 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161335740 | TAAATTCCTAGGAGT[A/G]GAATTACTGTGTTTA | 10213 |
rs796530337 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161347213 | CAAACTATTGTTTCA[C/T]AGAGTTTTGTCTGTT | 10213 |
rs796534401 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161316093 | AGGTGATCCGCCCGC[A/G]TTGGCCTCCCAAAGT | 10213 |
rs796547657 | snp | C/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161328950 | TTTTAGAAGAGCCAC[C/G]AAATAAAGTCAGAAA | 10213 |
rs796575957 | snp | A/C | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161366042 | AGTAAAATTATCATA[A/C]CACTAAAATTAGGTT | 10213 |
rs796607202 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394837 | GAGGAAGGTAAGTTA[C/T]GCAAAGATGAGAATA | 10213 |
rs796794238 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161354526 | TGTTGCAGTGGAGCA[C/T]GGTGATTGTTACCCA | 10213 |
rs796858199 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161342946 | ATACTACTTTATTTA[C/T]AGCATGTGAATGTTA | 10213 |
rs796885770 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161329683 | TAGAAACAAAGCAGA[A/T]TTACAAGATGCCTTT | 10213 |
rs796905539 | snp | A/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161341871 | TAAAATTAAAAAAAA[A/T]ATATATGTATATATA | 10213 |
rs796914264 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161311866 | GTGATCCAACCGCCT[C/T]GGCCTCCCAAAGAGC | 10213 |
rs796924886 | snp | G/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161394991 | TTAAGTCGAAATGTT[G/T]TTTTTTTTTTGAAGT | 10213 |
rs796938150 | snp | C/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161341915 | AATTATATTTTGATA[C/T]GATAATTAAGAAATC | 10213 |
rs796939966 | in-del | -/T | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161329502 | AATATTCTGGTTACC[-/T]TTTTTTTTCTTTGAG | 10213 |
rs796996262 | snp | A/G | | | intron-variant | PSMD14 | GRCh38.p7 | 2:161410213 | CCAGTGTTTCTCAGT[A/G]TTTTTCACCTAAAAT | 10213 |