SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11333 | snp | A/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130552 | TGTTCTTCTAGTTAT[A/T]TTAAAGAAAGCATAA | 51444 |
rs593234 | snp | C/T | 0.24019 | 0.249807 | intron-variant | RNF138 | GRCh38.p7 | 18:32099959 | TCACTAGAGCTGCAA[C/T]TATTCTTGTGTGATG | 51444 |
rs684359 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | RNF138 | GRCh38.p7 | 18:32129018 | GTGTGTGTAATGTGT[A/G]TCAAGATGTGTAATG | 51444 |
rs684693 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | RNF138 | GRCh38.p7 | 18:32101283 | tacagtgagccaaga[C/T]tgcgtgtgccactgc | 51444 |
rs865450 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | RNF138 | GRCh38.p7 | 18:32097557 | ggtgggatcttggtt[C/T]actgtaacctccacc | 51444 |
rs1054667 | snp | A/C | 0.490007 | 0.0699769 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131298 | AAATGATTGTTTAAA[A/C]TTTCCCCTCTTTTTG | 51444 |
rs1059390 | snp | A/T | 0 | 0 | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129169 | TGCTGTTGAAGAATC[A/T]TTTCAAGTAAACATC | 51444 |
rs1114052 | snp | A/C | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32126996 | TTGAGTTTACTCTCC[A/C]CCTCCTGTACTATAG | 51444 |
rs1814795 | snp | C/T | 0.446771 | 0.154211 | intron-variant | RNF138 | GRCh38.p7 | 18:32122606 | AGGTGGGCGGATCAC[C/T]TGAGCTCAGGAGTTC | 51444 |
rs2010813 | snp | A/G | 0.496681 | 0.0405994 | intron-variant | RNF138 | GRCh38.p7 | 18:32128336 | tgaggtcagcagttc[A/G]agaccagcctggcca | 51444 |
rs2048245 | snp | C/T | 0.489434 | 0.0719116 | intron-variant | RNF138 | GRCh38.p7 | 18:32111644 | TGTACATATGAGTAG[C/T]CTAACTTATTTAATA | 51444 |
rs2136405 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096920 | ACAAAGCAAGACCCA[A/T]CTCTACAAAAAAATT | 51444 |
rs3760567 | snp | A/G | 0.0283406 | 0.115616 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090021 | gaggccaaggtgggc[A/G]gatcgctggaggcca | 51444 |
rs3760568 | snp | A/G | 0.424193 | 0.179323 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091758 | GAAAACTTCCTGAAA[A/G]GCCCAATGTATTTGA | 51444 |
rs3834614 | in-del | -/TTAT | | | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091671 | GTAACAAATATTTGT[-/TTAT]AACACATCTTGACAA | 51444 |
rs3962083 | snp | C/T | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32127621 | AAATTCAAATATATG[C/T]AAAATTTAGGTGCGC | 51444 |
rs3980843 | snp | A/G | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32127312 | TGTAAAAATGAATTC[A/G]TAAAGCAAAATGGAT | 51444 |
rs3980844 | in-del | -/TT | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131379 | TATGGGGAAAAGTTT[-/TT]ATTTTTAATATTACT | 51444 |
rs4239373 | snp | C/T | 0.440884 | 0.161442 | intron-variant | RNF138 | GRCh38.p7 | 18:32122124 | cacccgcctcagcct[C/T]gcaaagtgctgggat | 51444 |
rs4239374 | snp | C/T | 0.197082 | 0.244335 | intron-variant | RNF138 | GRCh38.p7 | 18:32122262 | GTGAACTGAGTGTCA[C/T]TGGAATGGTGCCTTT | 51444 |
rs4799327 | snp | A/G | 0.287085 | 0.247234 | intron-variant | RNF138 | GRCh38.p7 | 18:32095029 | ATCAACTTATTGTAC[A/G]TAGACAGTTCTGCCT | 51444 |
rs4799328 | snp | A/T | 0.288906 | 0.246954 | intron-variant | RNF138 | GRCh38.p7 | 18:32122387 | TTTTATAAAGGAAAA[A/T]TGAATAACCAGTTTA | 51444 |
rs4799630 | snp | A/G | 0.287867 | 0.247116 | intron-variant | RNF138 | GRCh38.p7 | 18:32094606 | CATTACCCATCTGAC[A/G]TGAAAAAAAAAACGT | 51444 |
rs4799631 | snp | A/G | 0.441158 | 0.161117 | intron-variant | RNF138 | GRCh38.p7 | 18:32097902 | tatgtatatgtgtat[A/G]tatgtgtatttgtgt | 51444 |
rs4799632 | snp | C/T | 0.496714 | 0.0404017 | intron-variant | RNF138 | GRCh38.p7 | 18:32100930 | TTAAATTAAAATAAA[C/T]GCTCAGAAAAATGGT | 51444 |
rs5823831 | snp | A/C | 0.451483 | 0.148002 | intron-variant | RNF138 | GRCh38.p7 | 18:32121143 | TGTCTCAAAAAAAAA[A/C]AAAACAAAAAAAAAG | 51444 |
rs7228516 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RNF138 | GRCh38.p7 | 18:32111069 | acaggcgtgagccac[C/T]gtgcccggcAAAGCC | 51444 |
rs7229437 | snp | C/T | 0.289165 | 0.246913 | intron-variant | RNF138 | GRCh38.p7 | 18:32118230 | ggcattcttcatata[C/T]tctggatagtaatcc | 51444 |
rs7229690 | snp | A/G | 0.00454277 | 0.047442 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111885 | AAAATATAATGAGGA[A/G]GTTTTCTGGTAGCTG | 51444 |
rs7234604 | snp | C/T | 0.196771 | 0.244268 | intron-variant | RNF138 | GRCh38.p7 | 18:32110659 | TCTAGATCCCAGATA[C/T]ATATGTCTGTAATTT | 51444 |
rs7238559 | snp | C/G | 0.489837 | 0.0705577 | intron-variant | RNF138 | GRCh38.p7 | 18:32095830 | TACTAAGTACTGTTT[C/G]TCTGGAGACTTAATA | 51444 |
rs7243277 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | RNF138 | GRCh38.p7 | 18:32126500 | ATGTCTAAGATTTCT[C/T]ACTGTGTTAGATTAA | 51444 |
rs7505481 | snp | A/C | 0.089084 | 0.191327 | intron-variant | RNF138 | GRCh38.p7 | 18:32121148 | caaaaaaaaacaaaa[A/C]aaaaaaaaagcagat | 51444 |
rs8085407 | snp | C/T | 0.44651 | 0.154543 | intron-variant | RNF138 | GRCh38.p7 | 18:32102490 | acaggcgtgagccac[C/T]gtgcctggccCTTTT | 51444 |
rs8095867 | snp | A/G | 0.44252 | 0.159487 | upstream-variant-2KB, intron-variant | RNF138 | GRCh38.p7 | 18:32092596 | CCCGGCGCGTGCGGC[A/G]GTAGCGTCTCTGCGT | 51444 |
rs8096674 | snp | C/T | 0.0158469 | 0.0875917 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129712 | ACTATAAGAAAATTG[C/T]ATTTATATAACATTT | 51444 |
rs9953463 | snp | C/T | 0.447032 | 0.153878 | intron-variant | RNF138 | GRCh38.p7 | 18:32099096 | TGGGAGAATGCGTAA[C/T]GGAAATTCGTCTAGC | 51444 |
rs9954966 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | RNF138 | GRCh38.p7 | 18:32096658 | AAACTGAGGATTCAG[A/C]TCATCTGCAAATGAT | 51444 |
rs9962021 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | RNF138 | GRCh38.p7 | 18:32116071 | gaggcgatgatgatg[A/G]taggtcctcattgag | 51444 |
rs9963611 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF138 | GRCh38.p7 | 18:32095194 | tttttttttgagaca[C/T]ggtcttattctgttg | 51444 |
rs9964804 | snp | C/T | 0.185788 | 0.241613 | intron-variant | RNF138 | GRCh38.p7 | 18:32120587 | GTAATTGATTTTCTA[C/T]TGTTGAACCTATTCT | 51444 |
rs9967305 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | RNF138 | GRCh38.p7 | 18:32105751 | AAGTTAAAAAATTTC[A/C]ATATCGGAAGACCAC | 51444 |
rs9967524 | snp | A/T | 0.497749 | 0.0334707 | intron-variant | RNF138 | GRCh38.p7 | 18:32096907 | GGCTATTAAAAAAAA[A/T]TTTTTTGTAGAGATG | 51444 |
rs10048285 | snp | A/G | 0.490063 | 0.0697833 | intron-variant | RNF138 | GRCh38.p7 | 18:32125746 | AGACTAGCCTGGGCA[A/G]CATAGTGAGACCCTG | 51444 |
rs10048287 | snp | C/G | 0.490007 | 0.0699769 | intron-variant | RNF138 | GRCh38.p7 | 18:32125761 | ACATAGTGAGACCCT[C/G]TCTATTTAAAAATAA | 51444 |
rs10647693 | in-del | -/CTG | 0.440746 | 0.161604 | intron-variant | RNF138 | GRCh38.p7 | 18:32107349 | GCTGGTCTCGAACTC[-/CTG]AGCTCAGGCAGTCCG | 51444 |
rs10663913 | in-del | -/AAAAG | 0.4444 | 0.15719 | intron-variant | RNF138 | GRCh38.p7 | 18:32128081 | CTCAAAAAAGAAAAG[-/AAAAG]TAGGTGATCTAATTA | 51444 |
rs10775450 | snp | C/T | 0.441568 | 0.160629 | intron-variant | RNF138 | GRCh38.p7 | 18:32105920 | TGAAGCAAAGCACAT[C/T]AAAACATAGCTGAAT | 51444 |
rs10853418 | snp | C/T | 0.489434 | 0.0719116 | intron-variant | RNF138 | GRCh38.p7 | 18:32118664 | TGAAACCTTGTCTCT[C/T]CCAAAAATAGAAAAA | 51444 |
rs10853419 | snp | A/G | 0.489259 | 0.0724914 | intron-variant | RNF138 | GRCh38.p7 | 18:32118702 | GGCGTGGTGGTGCGC[A/G]CCTGTAATCCCAGCT | 51444 |
rs11081743 | snp | C/T | 0.34989 | 0.229177 | intron-variant | RNF138 | GRCh38.p7 | 18:32101231 | ttttttttttttttt[C/T]aaagacagagtctgg | 51444 |
rs11081744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32105804 | TGATGGACTGAATGT[C/T]GTCTGTTCTACTTGC | 51444 |
rs11081745 | snp | A/C | 0.133777 | 0.221342 | intron-variant | RNF138 | GRCh38.p7 | 18:32118753 | AGAATTCCTTGAACC[A/C]GGGAGGCCAAGGTTG | 51444 |
rs11081746 | snp | C/G | 0.490784 | 0.0672522 | intron-variant | RNF138 | GRCh38.p7 | 18:32124689 | GAGAGCGTTATTTTT[C/G]TGTTATTCTGAATTA | 51444 |
rs11307731 | in-del | -/T | 0.446771 | 0.154211 | intron-variant | RNF138 | GRCh38.p7 | 18:32113368 | CAGCCAGGAACTTAA[-/T]TTTTTTTTAAGTGCT | 51444 |
rs11375175 | in-del | -/A | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32103876 | AGGCTGAGGCAGGAG[-/A]ATGGTGTGAACCCTG | 51444 |
rs11441456 | in-del | -/T | 0.442249 | 0.159814 | intron-variant | RNF138 | GRCh38.p7 | 18:32094208 | TTTTCTTTTTTTTTT[-/T]GAGGTGAGGTTCTAT | 51444 |
rs11661197 | snp | G/T | 0.48955 | 0.071525 | intron-variant | RNF138 | GRCh38.p7 | 18:32116732 | AATTTTTTGATTTTT[G/T]GGGGTGGGGGGGTGG | 51444 |
rs11663518 | snp | A/C | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32110326 | TGTTAATTGGTAATG[A/C]CTTCTAGTGCTGCTT | 51444 |
rs11663563 | snp | A/G | 0.489608 | 0.0713316 | intron-variant | RNF138 | GRCh38.p7 | 18:32110463 | GTTGTAGATACTTTT[A/G]TTATTTCGTGAGTGA | 51444 |
rs12326277 | snp | A/G | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32124024 | GAAGTTAGCAGTTTA[A/G]AAATAGAAAATGCAG | 51444 |
rs12326287 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32124198 | GATGCTTGATCCTCA[A/G]AATGTTTTCGAGTAT | 51444 |
rs12326443 | snp | C/T | 0.127944 | 0.218179 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091282 | CTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTG | 51444 |
rs12455044 | snp | A/G | 0.439406 | 0.163173 | intron-variant | RNF138 | GRCh38.p7 | 18:32112688 | ACGCTGTCTAAAAAA[A/G]AAGAAGAAGAAAGAA | 51444 |
rs12458837 | snp | G/T | 0.439502 | 0.163061 | intron-variant | RNF138 | GRCh38.p7 | 18:32105283 | ttttagtagagacag[G/T]tttcaccatgttggc | 51444 |
rs12458851 | snp | C/G | 0.439918 | 0.162576 | intron-variant | RNF138 | GRCh38.p7 | 18:32105480 | TTTGGAACTTTTTAT[C/G]TTTGATAGACGTGAC | 51444 |
rs12604223 | snp | C/T | 0.440195 | 0.162252 | intron-variant | RNF138 | GRCh38.p7 | 18:32123776 | TCCTGCCTCAGCCTC[C/T]CAAGTATCTGGTATT | 51444 |
rs12605137 | snp | C/T | 0.49681 | 0.0398085 | intron-variant | RNF138 | GRCh38.p7 | 18:32107051 | TGTCTCCTATGGCTA[C/T]TGGGCCACTGGATTA | 51444 |
rs12606789 | snp | G/T | 0.126564 | 0.217402 | intron-variant | RNF138 | GRCh38.p7 | 18:32114966 | GTTCTCATTTTACTT[G/T]ACTTGTTAGTGTCAA | 51444 |
rs12607933 | snp | A/G | 0.126909 | 0.217598 | intron-variant | RNF138 | GRCh38.p7 | 18:32099533 | CCAATCTCCCGTGTA[A/G]CTGGAACTACAGGCA | 51444 |
rs12608245 | snp | G/T | 0.126909 | 0.217598 | intron-variant | RNF138 | GRCh38.p7 | 18:32126028 | AACTTTGGCTAGAGT[G/T]TAATTACTGAAGGTT | 51444 |
rs12955597 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102196 | ccTTCTTTTAGtttc[C/T]ttttttttttttttt | 51444 |
rs12961683 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121220 | ttcaatcctggccag[G/T]tgtggtggctcatgc | 51444 |
rs12962037 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098565 | TAATTATATAATAAA[A/G]GTTGAggccgggcgc | 51444 |
rs12962038 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098569 | TATATAATAAAGGTT[G/T]Aggccgggcgcagtg | 51444 |
rs12962040 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098579 | AGGTTGAggccgggc[C/G]cagtggctcacgcct | 51444 |
rs12962043 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098582 | TTGAggccgggcgca[A/G]tggctcacgcctgtc | 51444 |
rs12962902 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107112 | AATTCACTTTCCttt[G/T]ttccttttttttttt | 51444 |
rs12963443 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF138 | GRCh38.p7 | 18:32125121 | ATGAACCGGGAACTC[A/G]TTCCTGCGCAGTAGC | 51444 |
rs12965634 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | RNF138 | GRCh38.p7 | 18:32113267 | tttgccatattgctc[A/G]ggctggtcttgaacc | 51444 |
rs12966132 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32089992 | ggctcaggcctgtaa[G/T]tccagcactttggga | 51444 |
rs12967984 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32092897 | CACGTGTGAGTAGAC[A/G]CCCCCTCCCCCTCGC | 51444 |
rs12968984 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108669 | tatatgtaAtttttg[G/T]tttgtttggttttta | 51444 |
rs12968986 | snp | G/T | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32108674 | gtaAtttttgttttg[G/T]ttggtttttaaatag | 51444 |
rs12969755 | snp | A/G | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32096497 | AAGTGGTCACCGAGT[A/G]AGGTATATAAATGGA | 51444 |
rs12969756 | snp | G/T | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32096500 | TGGTCACCGAGTGAG[G/T]TATATAAATGGAAAG | 51444 |
rs12970529 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096473 | ATGGAGCTAAAGCTG[G/T]GGGTGTCGAAGTGGT | 51444 |
rs13381692 | snp | G/T | 0.0329836 | 0.124112 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131781 | TTTTATGAAGTGTCT[G/T]CGGAGCAAGATTTTC | 51444 |
rs16962689 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | RNF138 | GRCh38.p7 | 18:32110655 | GTATTCTAGATCCCA[C/G]ATATATATGTCTGTA | 51444 |
rs16962691 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | RNF138 | GRCh38.p7 | 18:32111152 | AAATTTCCCTACTTC[C/T]GGACCAAATAACCAA | 51444 |
rs16962693 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32111200 | GATAACTTTGGGTAA[A/C]ACCTAACTTTGGGTA | 51444 |
rs16962696 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | RNF138 | GRCh38.p7 | 18:32111578 | TCTAGTCCAGTTATC[A/C]GTCTTACTCTCTGAT | 51444 |
rs16962698 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | RNF138 | GRCh38.p7 | 18:32112358 | GGAACTCTCTAGCTC[C/G]TCACTTTACTTATGT | 51444 |
rs16962699 | snp | A/G | 0.192401 | 0.243274 | intron-variant | RNF138 | GRCh38.p7 | 18:32112911 | AATTCAGTGAGCAAA[A/G]CTGGTTGCTATTTCA | 51444 |
rs16962700 | snp | A/C | 0.123105 | 0.215401 | intron-variant | RNF138 | GRCh38.p7 | 18:32113559 | CTTCTCCATCTCTAC[A/C]TTTAATGAACAGAAA | 51444 |
rs16962701 | snp | C/G | 0.289424 | 0.246872 | intron-variant | RNF138 | GRCh38.p7 | 18:32115148 | GGTGTTTGTCTTGTT[C/G]AGCATATCTCCAGCT | 51444 |
rs16962717 | snp | A/T | 0.0596104 | 0.162024 | intron-variant | RNF138 | GRCh38.p7 | 18:32123139 | TTGAAGTAAAAAAGT[A/T]CACAAATTCTTGAGT | 51444 |
rs16962718 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RNF138 | GRCh38.p7 | 18:32124170 | CTGAAATTCAGAAGT[A/G]TTAAAACTCAGTGAT | 51444 |
rs16962721 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF138 | GRCh38.p7 | 18:32127690 | ATTATTAAATTCTCA[C/T]TGTAAGAAAGATTGC | 51444 |
rs17719020 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | RNF138 | GRCh38.p7 | 18:32109023 | ATTTATGCGCTCTAA[G/T]GGATATTGCCACCCA | 51444 |
rs17735362 | snp | G/T | 0.0926964 | 0.194308 | intron-variant | RNF138 | GRCh38.p7 | 18:32123390 | ACCCAATAGGAAAAA[G/T]GTGTATTGAAGTTCA | 51444 |
rs17742539 | snp | A/C | 0.127254 | 0.217792 | intron-variant | RNF138 | GRCh38.p7 | 18:32124296 | CCTGGTATTTATTAG[A/C]GATACGATATTGATG | 51444 |
rs28364713 | in-del | -/G | 0.124517 | 0.216227 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092630 | GCCCCGCCCTACCCA[-/G]GGCCCCGCCCCCTTC | 51444 |
rs28375522 | snp | A/T | 0.040671 | 0.13668 | intron-variant | RNF138 | GRCh38.p7 | 18:32104557 | GATTAAAAACAAGAG[A/T]AACAATAAGAGTACA | 51444 |
rs28378426 | snp | A/G | 0.446118 | 0.155041 | intron-variant | RNF138 | GRCh38.p7 | 18:32107941 | CTCACTGCAAGCTCC[A/G]CCTCCCAGGTACGAG | 51444 |
rs28440020 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | RNF138 | GRCh38.p7 | 18:32099552 | GAACTACAGGCATGC[A/C]CCACTATACCCGGCT | 51444 |
rs28538314 | snp | G/T | 0.0283406 | 0.115616 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091547 | AACCCAAAGGTGTAG[G/T]AGAAGACTGCATCTG | 51444 |
rs28556958 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF138 | GRCh38.p7 | 18:32108409 | GTACATTCTAAAAAA[C/T]AGAATCGTGCAGTTT | 51444 |
rs28574941 | snp | C/T | 0.206642 | 0.246211 | intron-variant | RNF138 | GRCh38.p7 | 18:32093592 | TTACCTTTCTGCTTA[C/T]TTATTACTTGATTAA | 51444 |
rs28596473 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | RNF138 | GRCh38.p7 | 18:32096224 | GAGCAGCGTGGTCAC[A/G]TTTCATTTTTAGAAA | 51444 |
rs28674120 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | RNF138 | GRCh38.p7 | 18:32124161 | TGTCCCTTCCTGAAA[A/T]TCAGAAGTATTAAAA | 51444 |
rs28727388 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | RNF138 | GRCh38.p7 | 18:32097617 | TCCTCCTGAGTAGCT[A/G]GGACTACAGGCACAA | 51444 |
rs33944288 | in-del | -/A | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32103877 | GGCTGAGGCAGGAGA[-/A]TGGTGTGAACCCTGG | 51444 |
rs34048134 | in-del | -/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126609 | TTTTTGGTAACATAT[-/C]CCCTGTGTTATTTTA | 51444 |
rs34156082 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104048 | AGGCAGAGTCTAGTT[A/C]TGTCGCCCATGCCAG | 51444 |
rs34201822 | in-del | -/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128997 | GTTTTACATAACTGT[-/C]CCTGAGTGTGTGTAA | 51444 |
rs34225221 | in-del | -/AT | 0.259951 | 0.249802 | intron-variant | RNF138 | GRCh38.p7 | 18:32100202 | GTGTTAGTGATTGAG[-/AT]ATATATATATATATA | 51444 |
rs34263941 | in-del | -/TT | 0.441158 | 0.161117 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131376 | ATTTATGGGGAAAAG[-/TT]TTTATTTTTAATATT | 51444 |
rs34510063 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114204 | CTTTTCAGTAATGTA[-/T]TTTGCAAACTACAAC | 51444 |
rs34563658 | snp | A/G | 0.145305 | 0.227022 | intron-variant | RNF138 | GRCh38.p7 | 18:32106173 | TTTTCAGAATTGTTC[A/G]TATTTTTATTTGGAT | 51444 |
rs34809791 | in-del | -/AAAAG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128082 | CCGTCTCAAAAAAGA[-/AAAAG]AAAGTAGGTGATCTA | 51444 |
rs34814991 | in-del | -/TG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097945 | ATGTGTATGTATATA[-/TG]TGTGTGTGTGTGTGT | 51444 |
rs34907696 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094257 | AAAGGATGGATTGAA[-/T]TTTTGGTTCTTAATT | 51444 |
rs35035401 | in-del | -/A | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095181 | TAAAAATTATCGTTT[-/A]TTTTTTGAGACATGG | 51444 |
rs35089739 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | RNF138 | GRCh38.p7 | 18:32106524 | TGGAAGATACTAGAA[G/T]TTGAAAAATTATTTT | 51444 |
rs35104806 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112302 | CAGCTTTACACATAG[-/T]AAATGTTACTAGTTT | 51444 |
rs35430156 | in-del | -/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122110 | TGACCTTGTGATCCA[-/C]CCCGCCTCAGCCTTG | 51444 |
rs35456809 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095336 | TCCATGCCTGACTAA[-/T]TTTTGTTTTCTTTTT | 51444 |
rs35497913 | in-del | -/TGT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097975 | GTGTGTGTGTGTGTG[-/TGT]TATTTTTGTTTGTTT | 51444 |
rs35738675 | in-del | -/A | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099267 | TTCTGCTTTGTTTTG[-/A]AAATAAGTTCTGTCT | 51444 |
rs35818174 | in-del | -/A | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32095180 | TTAAAAATTATCGTT[-/A]TTTTTTTGAGACATG | 51444 |
rs36019706 | snp | A/G | 0.146314 | 0.227484 | intron-variant | RNF138 | GRCh38.p7 | 18:32099406 | GACCTGAATATCTCT[A/G]TTTTATTTTATTTTT | 51444 |
rs36074374 | in-del | -/ATT | 0.489434 | 0.0719116 | utr-variant-3-prime, cds-indel, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129483 | ATTTTTGAATTTTTC[-/ATT]ATTATGTTGCTTTTG | 51444 |
rs36090316 | in-del | -/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106047 | GCATGTTTCTCCTTT[-/C]CCCTTGTGCATTTTA | 51444 |
rs55912779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111667 | ATTTAATATGAATAC[A/G]TATTTATAATCACTT | 51444 |
rs55948956 | snp | A/G | 0.040671 | 0.13668 | intron-variant | RNF138 | GRCh38.p7 | 18:32114666 | AATTTTGAAAACTTC[A/G]GTAGTAAGCACATAC | 51444 |
rs56273402 | snp | C/G | 0.193028 | 0.243422 | intron-variant | RNF138 | GRCh38.p7 | 18:32106747 | TTTTTTGTATTTTTA[C/G]TAGAGACAGGGTTTC | 51444 |
rs56277951 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | RNF138 | GRCh38.p7 | 18:32121033 | CCAGCTACTCGGGAG[A/G]CTGAGGCACGAGAAT | 51444 |
rs57166978 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | RNF138 | GRCh38.p7 | 18:32121090 | CAATTAGCCGCGATC[A/G]CGCCGCTGCACTCCA | 51444 |
rs57482240 | in-del | -/TAT | | | utr-variant-3-prime, cds-indel, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129488 | TGAATTTTTCATTAT[-/TAT]GTTGCTTTTGAAATT | 51444 |
rs57941620 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32109544 | CTCCCAAGTGGCTAA[A/G]ACTACAGGTACATGC | 51444 |
rs57992536 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF138 | GRCh38.p7 | 18:32095863 | CCGCTGGAGAGACCT[A/G]TAAATGAGTGTGATT | 51444 |
rs58298513 | in-del | -/TT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098915 | GTTTACAACCTTTGA[-/TT]TTTTTTTTTTTTGAA | 51444 |
rs58517415 | in-del | -/ATTT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106575 | TTTATTTATTTATTT[-/ATTT]GTTTATTGAGATGGA | 51444 |
rs58774714 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107116 | ACTTTCCTTTTTTCC[-/T]TTTTTTTTTTTTTTT | 51444 |
rs58803750 | in-del | -/A/AA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123981 | AAAAAAAAAAAAAAA[-/A/AA]TCAGTTACATCATTA | 51444 |
rs59015789 | in-del | -/GA | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130920 | AGCTCCTTTTTAAGA[-/GA]CTTTTGACCATAGTG | 51444 |
rs59055673 | in-del | -/T/TTA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101230 | TTTTTTTTTTTTTTT[-/T/TTA]CAAAGACAGAGTCTG | 51444 |
rs59172119 | in-del | -/C | 0.375598 | 0.21616 | intron-variant | RNF138 | GRCh38.p7 | 18:32121143 | TGTCTCAAAAAAAAA[-/C]AAAACAAAAAAAAAG | 51444 |
rs59343680 | snp | A/G | 0.131723 | 0.220251 | intron-variant | RNF138 | GRCh38.p7 | 18:32094609 | TACCCATCTGACATG[A/G]AAAAAAAAACGTTTG | 51444 |
rs59383566 | in-del | -/G | 0.19646 | 0.2442 | intron-variant | RNF138 | GRCh38.p7 | 18:32114876 | TCAGTTGAAATTTCT[-/G]GGTAAAAACCTTTAG | 51444 |
rs59577480 | snp | C/T | 0.040671 | 0.13668 | intron-variant | RNF138 | GRCh38.p7 | 18:32110970 | TATTTTTAGTAGAGA[C/T]GAGATTTCACCGTGG | 51444 |
rs59690483 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108964 | TAAGCCACTGCCCAT[A/G]GTTTTATGTATATAG | 51444 |
rs59741272 | snp | C/T | 0.117188 | 0.211804 | intron-variant | RNF138 | GRCh38.p7 | 18:32116993 | TACAACATCGACCTC[C/T]CAGGTTCAAGTGATT | 51444 |
rs59810035 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | RNF138 | GRCh38.p7 | 18:32094879 | GTAGTTTTTAGCACT[C/T]CCCAAAATTCCGTGT | 51444 |
rs59911054 | snp | A/G | 0.124491 | 0.216211 | intron-variant | RNF138 | GRCh38.p7 | 18:32096853 | CACCTCAACCTCCCA[A/G]GTAGCTAGCTGGGAC | 51444 |
rs60139696 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096906 | TGGCTATTAAAAAAA[A/T]TTTTTTTGTAGAGAT | 51444 |
rs60269639 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | RNF138 | GRCh38.p7 | 18:32109895 | TGTCTCAAAAAAATA[A/G]AATAAATAAAACTAG | 51444 |
rs60334586 | in-del | -/CAAAGTTTAATACATCCAATATGTCAAGTTAAACCATTCTGGGATTTG | | | utr-variant-3-prime, cds-indel, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131069 | CCATTCTGGGATTTG[lengthTooLong]GGAACTTCTTTAAAG | 51444 |
rs60507961 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | RNF138 | GRCh38.p7 | 18:32109744 | GTACAAAAATTAGCC[A/G]TCGCAGTGGTGCATG | 51444 |
rs60789951 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095929 | GGTATCTAAATTAGC[C/T]TAAAGGATAGGGATA | 51444 |
rs61018724 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32109323 | CATGCCAGGCTAGTA[A/G]AGATGGGGTTTCACC | 51444 |
rs61067505 | in-del | -/GTT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097976 | TGTGTGTGTGTGTGT[-/GTT]ATTTTTGTTTGTTTG | 51444 |
rs61198143 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101522 | TTTATTTTTTTAAGC[C/T]TTAGTTTCCTCATCT | 51444 |
rs61271315 | snp | A/G | 0.287346 | 0.247195 | intron-variant | RNF138 | GRCh38.p7 | 18:32099597 | TTTAGTAGAGATGGT[A/G]TTGCACCATGTTGGT | 51444 |
rs61555941 | in-del | -/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116744 | TTTGGGGTGGGGGGG[-/G]TGGTTTTTGGTGTTA | 51444 |
rs61709171 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | RNF138 | GRCh38.p7 | 18:32095445 | CAAAAGTGCTGGGAT[A/G]ACAGGCGTGAGGCAT | 51444 |
rs62093949 | snp | C/T | 0.440471 | 0.161928 | intron-variant | RNF138 | GRCh38.p7 | 18:32093393 | TTCAGAACCTTGGTC[C/T]GTCCCCTCGGTCCAA | 51444 |
rs62093950 | snp | A/G | 0.439918 | 0.162576 | intron-variant | RNF138 | GRCh38.p7 | 18:32100331 | GGGTCTTTCTCTGTT[A/G]CTCTGTTGCCCAGGC | 51444 |
rs62095571 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102499 | AGCCACTGTGCCTGG[C/T]CCTTTTTTTTAGTTT | 51444 |
rs62095572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102779 | CTGGGATTACAGGTG[C/T]GCAACACCACGCCCA | 51444 |
rs62095573 | snp | G/T | 0.0433465 | 0.140692 | intron-variant | RNF138 | GRCh38.p7 | 18:32108986 | TGTATATAGGTTTGA[G/T]GGGTATATACTTCAG | 51444 |
rs71177843 | in-del | -/GGGAGAGC | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32093143 | GGGGCGCGAAAGCCA[-/GGGAGAGC]GGGAGAGCGGGAGAG | 51444 |
rs71177844 | in-del | -/T | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32098561 | CCGGCCTCAACCTTT[-/T]ATTATATAATTAAAT | 51444 |
rs71361367 | snp | G/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32126653 | TATAATATTTCATTG[G/T]TTTTATTATTTTTTG | 51444 |
rs71384925 | in-del | -/CC | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32119719 | TGAGCCACTGCCCCC[-/CC]AGCCTCTTTCTCATT | 51444 |
rs71384926 | in-del | -/C | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32119723 | GCCACTGCCCCCAGC[-/C]TCTTTCTCATTTAAA | 51444 |
rs71794147 | in-del | -/CTG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107350 | CTGGTCTCGAACTCA[-/CTG]GCTCAGGCAGTCCGC | 51444 |
rs72936933 | snp | A/G | 0.131381 | 0.220067 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091673 | AACAAATATTTGTTT[A/G]TAACACATCTTGACA | 51444 |
rs72936945 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | RNF138 | GRCh38.p7 | 18:32097272 | CAATAAAAATTACAT[A/G]TAACAAGTTTGATTC | 51444 |
rs72940728 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | RNF138 | GRCh38.p7 | 18:32102538 | AATGTTTTTAATAAT[A/G]TCACTAGTCTGTAGT | 51444 |
rs72940731 | snp | C/G | 0.114387 | 0.210022 | intron-variant | RNF138 | GRCh38.p7 | 18:32106185 | TTCGTATTTTTATTT[C/G]GATTGTTTGGGTTTT | 51444 |
rs73415858 | snp | A/G | 0.19334 | 0.243495 | intron-variant | RNF138 | GRCh38.p7 | 18:32102681 | TCCGTTGCCCAGGCT[A/G]GAGTACAGTGGCACT | 51444 |
rs73415859 | snp | C/G | 0.19334 | 0.243495 | intron-variant | RNF138 | GRCh38.p7 | 18:32103985 | AAAAAAAGAAAACTT[C/G]ATAGCAAATTAGGAA | 51444 |
rs73415860 | snp | A/T | 0.193028 | 0.243422 | intron-variant | RNF138 | GRCh38.p7 | 18:32104322 | CTGGCCTAAAAGTTT[A/T]AAAAAAAAAATCCTC | 51444 |
rs73954995 | snp | G/T | 0.040671 | 0.13668 | intron-variant | RNF138 | GRCh38.p7 | 18:32099282 | GAAATAAGTTCTGTC[G/T]AGCACTTTGATCCAT | 51444 |
rs74430901 | snp | A/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32123980 | TAAAAAAAAAAAAAA[A/T]ATCAGTTACATCATT | 51444 |
rs74520392 | snp | A/T | 0.126909 | 0.217598 | intron-variant | RNF138 | GRCh38.p7 | 18:32104635 | ACCAGCAGTAATCAG[A/T]TAAAAAATTAATAGA | 51444 |
rs74563380 | snp | A/G/T | 0.0107246 | 0.0724382 | intron-variant | RNF138 | GRCh38.p7 | 18:32093680 | GATGCTACCCAGGGT[A/G/T]GGGGAGAACACAAAG | 51444 |
rs74760307 | snp | G/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32111723 | GAGAGTAATTTTTTT[G/T]GTAATTAATGTGTCA | 51444 |
rs74805307 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107849 | AACAGTTTTAATATA[A/T]CTACCCTTGTTTAAA | 51444 |
rs74893619 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | RNF138 | GRCh38.p7 | 18:32128957 | AGGTATTCAAATCTT[C/G]TATCTTAAAAGATAC | 51444 |
rs74958430 | snp | G/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32102651 | TTTTCTTTTTTTTTT[G/T]AGAAATAGTCTCCTT | 51444 |
rs75069983 | snp | A/T | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32096701 | AGTCAGCATTTTCAG[A/T]GGCCTTAGAGTGGTC | 51444 |
rs75198676 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32104295 | TGAGATTACATGCAT[A/G]AGCCACCAGACCTGG | 51444 |
rs75357756 | snp | A/T | 0.126564 | 0.217402 | intron-variant | RNF138 | GRCh38.p7 | 18:32114155 | TTCTCTTACTGATTT[A/T]GCAACTGAAATGATT | 51444 |
rs75487176 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096490 | GGTGTCGAAGTGGTC[A/T]CCGAGTGAGGTATAT | 51444 |
rs75579957 | snp | G/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32102650 | ATTTTCTTTTTTTTT[G/T]GAGAAATAGTCTCCT | 51444 |
rs75833412 | snp | A/C | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32104857 | TGGTGAAGTCCCAAC[A/C]TGATTTTTTGGTAGA | 51444 |
rs75902316 | snp | A/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32104332 | AGTTTAAAAAAAAAA[A/T]TCCTCATTAAGGGTG | 51444 |
rs75915001 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | RNF138 | GRCh38.p7 | 18:32101812 | TACAGTTCATAGTGG[G/T]GTCTAGAAGTCACAT | 51444 |
rs75950558 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | RNF138 | GRCh38.p7 | 18:32095264 | AGCCTTGACCTCCCC[C/T]GTTGGAGCAACCCTC | 51444 |
rs76056760 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129586 | ATGTGATTGATATAA[C/T]CTAACAAATCTGAGC | 51444 |
rs76121406 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RNF138 | GRCh38.p7 | 18:32108375 | TATCCTGACCTTTAA[C/T]ATAGTTTAAGTGCTT | 51444 |
rs76123091 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | RNF138 | GRCh38.p7 | 18:32102791 | GTGCGCAACACCACG[A/C]CCAGCTAATTTTTAT | 51444 |
rs76132324 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF138 | GRCh38.p7 | 18:32094559 | GGCATGTGTGAGATA[C/T]GCCATCCTCAAACCT | 51444 |
rs76178144 | snp | A/C | | | missense, synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32123518 | CCTGTGCTTCTTAAG[A/C]AATAGGAGTGAAACA | 51444 |
rs76275490 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | RNF138 | GRCh38.p7 | 18:32101631 | CAGCCTAGCACCTAG[C/T]ACATATTATGTACGC | 51444 |
rs76402810 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF138 | GRCh38.p7 | 18:32101646 | CACATATTATGTACG[C/T]AATAAGTGTTAACTG | 51444 |
rs76450674 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096489 | GGGTGTCGAAGTGGT[A/C]ACCGAGTGAGGTATA | 51444 |
rs76586220 | snp | G/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32111999 | ATTTTCTTGGTTGGT[G/T]TTTTTTTTTTTTTTG | 51444 |
rs76852201 | in-del | -/AA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098868 | AAAAAAAAAAAAAAA[-/AA]GATTTACTTAATTTT | 51444 |
rs76945426 | in-del | -/CTTAT | 0.437542 | 0.165312 | intron-variant | RNF138 | GRCh38.p7 | 18:32122474 | TTTTCTTAGCCACTA[-/CTTAT]CTTATTACTGTGTTA | 51444 |
rs76945554 | snp | A/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32099584 | ATTTTTTTGTATTTT[A/T]AGTAGAGATGGTGTT | 51444 |
rs77015924 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32115295 | TGATTCCTAATAGCA[A/G]TATTCCTCATCTGTA | 51444 |
rs77056537 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094207 | CCTTCGACTTTTTTT[C/T]CTTTTTTTTTTGAGG | 51444 |
rs77146499 | snp | A/T | 0.0596104 | 0.162024 | intron-variant | RNF138 | GRCh38.p7 | 18:32124398 | ATTTTCAAGGGACAT[A/T]CAGTGACAGCTATTG | 51444 |
rs77336940 | snp | C/G | 0.0111196 | 0.0737302 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090585 | AAAGTTTTCTGTTAA[C/G]TCTATATATTTCTAA | 51444 |
rs77410034 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107848 | TAACAGTTTTAATAT[A/C]ACTACCCTTGTTTAA | 51444 |
rs77654972 | snp | C/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32101216 | CTCTTATAGGTTTCT[C/T]TTTTTTTTTTTTTTC | 51444 |
rs77670909 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | RNF138 | GRCh38.p7 | 18:32125832 | ACCTTAAGCTCTCAC[A/T]TACCACCTAAGAAGG | 51444 |
rs77748625 | snp | A/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32101790 | AAGCATTTTTATGCT[A/T]TTTTAATACAGTTCA | 51444 |
rs77777706 | in-del | -/CTTAT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122479 | TTAGCCACTACTTAT[-/CTTAT]TACTGTGTTAAGATT | 51444 |
rs77865261 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32113208 | CCCCACAGGTAGCTG[A/G]GATTACACCTGGCTA | 51444 |
rs78042113 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32116034 | TGCCTCAGTTGTCTC[A/G]TGTGTTTAAGGAAAG | 51444 |
rs78071298 | snp | A/G | | | missense, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32123528 | TTAAGCAATAGGAGT[A/G]AAACATCCACATCTG | 51444 |
rs78501371 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32104259 | GTCAAATGATCCCCC[A/C/G]ACTTCGGCGTCCCAA | 51444 |
rs78914503 | snp | A/G | 0.147656 | 0.228091 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091713 | CATTCTGGTAGGGCA[A/G]ATAGTAAAGACTAAA | 51444 |
rs79115710 | in-del | -/GA | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130919 | CAGCTCCTTTTTAAG[-/GA]ACTTTTGACCATAGT | 51444 |
rs79235489 | snp | A/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32104333 | GTTTAAAAAAAAAAA[A/T]CCTCATTAAGGGTGG | 51444 |
rs79421604 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF138 | GRCh38.p7 | 18:32115782 | ACGCACGCACGCACA[C/T]ACACACTTCCTTATT | 51444 |
rs79509827 | snp | A/G | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32099585 | TTTTTTTGTATTTTT[A/G]GTAGAGATGGTGTTG | 51444 |
rs79546740 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091277 | CCGGCCTTTTTTCTT[C/T]CTTTTTTTTTTTTTT | 51444 |
rs79549415 | snp | A/C | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32121133 | AGAGTGAGACTGTCT[A/C]AAAAAAAAACAAAAC | 51444 |
rs79629457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32111250 | TAGAACTTCCCAAAC[C/T]AATTTGTGTGCTCTT | 51444 |
rs79777666 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32120031 | ATAGTTTTGTCTGCT[G/T]CTTTTAAACCTAATG | 51444 |
rs79895200 | snp | C/G | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32099844 | ACTTACTTAAGCCTA[C/G]TAATATATCGTTTCA | 51444 |
rs80105716 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | RNF138 | GRCh38.p7 | 18:32125129 | GGAACTCATTCCTGC[A/G]CAGTAGCACAACCTG | 51444 |
rs80165292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108594 | CCTATGTATAGTTTT[C/G]AGTTTGGGGCTATTA | 51444 |
rs80178095 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094208 | CTTCGACTTTTTTTT[C/T]TTTTTTTTTTGAGGT | 51444 |
rs111272154 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093143 | CTCTCCCGCTCTCCC[G/T]CTCTCCCTGGCTTTC | 51444 |
rs111326895 | snp | A/C | 0.109108 | 0.206518 | intron-variant | RNF138 | GRCh38.p7 | 18:32128479 | GGAGGTGGAGGTTGC[A/C]GTGAGCCAAGATTGT | 51444 |
rs111343940 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | RNF138 | GRCh38.p7 | 18:32122237 | AGATAACATTGTTAT[C/T]TTCACAGAAGTGAAC | 51444 |
rs111355456 | snp | A/C | 0.192715 | 0.243348 | intron-variant | RNF138 | GRCh38.p7 | 18:32092978 | CCGCCTGGCGGGAAC[A/C]GAGCCCGCCGCGGCC | 51444 |
rs111410574 | snp | C/T | 1.6577e-05 | 0.00287893 | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32123569 | AACTTACCAAGAGAA[C/T]ACAAGGTAAGCTTTT | 51444 |
rs111482418 | in-del | -/AT | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32100201 | GTGTTAGTGATTGAG[-/AT]ATATATATATATATA | 51444 |
rs111505733 | snp | A/T | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32116911 | TTTTTATTTTTAATT[A/T]ATTTATTTGTAGACA | 51444 |
rs111517421 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129126 | GTTTTTAGAATCTTC[A/G]GCTAGATGAAGAAAC | 51444 |
rs111684677 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32093989 | GTAGAGACGGGGTTT[C/T]ACCGTGTTAGCAAGG | 51444 |
rs111887117 | in-del | -/T | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32115014 | TTATAGTTTTTTTTT[-/T]AGTCCTTCTGGGTTT | 51444 |
rs111968861 | snp | C/G | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32115736 | GGCGACAGAGTCAGA[C/G]TCCGTCTAAAACACA | 51444 |
rs112004208 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095180 | TTTAAAAATTATCGT[A/T]TTTTTTTGAGACATG | 51444 |
rs112049552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32110350 | GCTGCTTTAATGATA[C/T]TAACTACTATTTATT | 51444 |
rs112165520 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RNF138 | GRCh38.p7 | 18:32119358 | TCCCGCCTTGGCCTC[C/T]TAAAGTGTTGGGATC | 51444 |
rs112201790 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32092971 | CGGGCTGCCGCCTGG[C/G]GGGAACCGAGCCCGC | 51444 |
rs112291721 | snp | A/G | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32114901 | CTTTAGTGATTGTCT[A/G]GTAAAGATCTGCAGT | 51444 |
rs112294481 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123907 | ATCCACCTGCCTTGG[A/C]CTCCCAAAGTGCTGG | 51444 |
rs112309785 | snp | C/T | 0.0640965 | 0.167152 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092154 | GGCCGGACAGGAAGC[C/T]CGAGGAAAGCGCTGG | 51444 |
rs112355865 | in-del | -/TTTA/TTTATTTA | 0.0193772 | 0.0965046 | intron-variant | RNF138 | GRCh38.p7 | 18:32106548 | TATTTTTTATTTTAT[-/TTTA/TTTATTTA]TTTATTTATTTATTT | 51444 |
rs112456567 | snp | A/G | 0.126909 | 0.217598 | intron-variant | RNF138 | GRCh38.p7 | 18:32121899 | TTCAGACTGAGTTTC[A/G]CTCTTGTTGCCCAGG | 51444 |
rs112526390 | snp | A/C | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32126573 | TGGAACTTGGCCTTT[A/C]AAAATGCTTCTCACG | 51444 |
rs112549625 | snp | C/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32114043 | TTGGCACACGTAAGC[C/T]CTCATCTGGGAGATG | 51444 |
rs112720620 | in-del | -/TTTA | 0.192088 | 0.2432 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091670 | CGTAACAAATATTTG[-/TTTA]TAACACATCTTGACA | 51444 |
rs112725008 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | RNF138 | GRCh38.p7 | 18:32100668 | TTAATAGAGACGGGG[G/T]TTTCACCATGTTGGT | 51444 |
rs112741267 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090305 | AAAATTTGAACTCAA[A/G]GAACCATTTTATAAG | 51444 |
rs112890433 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | RNF138 | GRCh38.p7 | 18:32120892 | CTCATGTCTGTAATC[C/T]CTGTACTTTGGGAGG | 51444 |
rs112918054 | snp | A/G | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32123606 | TCCTGCCACTTTAGC[A/G]AGTAATATTATATTT | 51444 |
rs112923970 | snp | C/T | 0.118933 | 0.212888 | intron-variant | RNF138 | GRCh38.p7 | 18:32100813 | TTTCACCATGTTGGC[C/T]GGGCTGGTCTCGAAT | 51444 |
rs112958659 | snp | A/G | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32108352 | TCCCACCTCCTTCAG[A/G]ATACCATTATCCTGA | 51444 |
rs113007576 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129136 | TCTTCAGCTAGATGA[A/G]GAAACCCAATACCAA | 51444 |
rs113013710 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | RNF138 | GRCh38.p7 | 18:32099970 | AATAATTGCAGCTCT[A/G]GTGAAGTGTCTTGTT | 51444 |
rs113016159 | snp | C/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32122153 | ATTACAGGTGTGAGC[C/T]ACTGTGCCCGGCCTG | 51444 |
rs113092348 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32096185 | ATGAATAATACTAGA[C/T]CTAGTAAATAATTTT | 51444 |
rs113107562 | snp | C/T | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32123674 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTTTGT | 51444 |
rs113345672 | in-del | -/A | 0.00835141 | 0.0640778 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091427 | AAATAAAATAAAATT[-/A]AAAAAAAACACTTAA | 51444 |
rs113539215 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | RNF138 | GRCh38.p7 | 18:32097743 | GGCCAGGCTGGTCTC[A/G]AACCCCTGCGCTCAA | 51444 |
rs113664706 | snp | A/G | 0.192715 | 0.243348 | intron-variant | RNF138 | GRCh38.p7 | 18:32098780 | ATGGCATGAACCCGG[A/G]AGGTGGAGCTTGCAG | 51444 |
rs113870783 | snp | G/T | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32125676 | GGTGGCTCATGCCTG[G/T]AATTTAGCACTTTGG | 51444 |
rs113887099 | snp | C/T | 0.5 | 0 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131607 | GCAAACATTTAACTC[C/T]CATAATTCACACTGA | 51444 |
rs113897874 | in-del | -/GTTT | 0.5 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32128986 | CTGTTATATATGTTT[-/GTTT]TACATAACTGTCCTG | 51444 |
rs114033819 | snp | C/T | 0.0271762 | 0.113356 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091923 | CACCCCGTGCCTCCC[C/T]GCCTCTCCTGGCTCC | 51444 |
rs114034136 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | RNF138 | GRCh38.p7 | 18:32097648 | CAAGTAGCTGGACTA[C/G]AGGCATGCACCACCA | 51444 |
rs114104374 | snp | G/T | 0.0424043 | 0.139298 | utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092713 | AGGGAGTCGGGCCCC[G/T]GGCCGCCACCGTCAC | 51444 |
rs114142866 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32128422 | ACGTATCTGTAATCC[C/T]AGCTACTTGGCAGGC | 51444 |
rs114242877 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129424 | GTTTCACTAATGTAA[C/T]GGTGAAAGAGAATCC | 51444 |
rs114274133 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32094328 | TTCTCATTTTTTCCC[C/T]AATCTTAACTGCACT | 51444 |
rs114281363 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | RNF138 | GRCh38.p7 | 18:32117591 | GCTGGACACACTCCA[C/T]GTTATGAATATACGG | 51444 |
rs114331246 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | RNF138 | GRCh38.p7 | 18:32111122 | CAAATTATGTTCCAT[C/T]GCATACTGTTTGGGA | 51444 |
rs114483659 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | RNF138 | GRCh38.p7 | 18:32118982 | TTTTCTTTTTATATC[A/G]TGCCTGAGAAATTTT | 51444 |
rs114681478 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | RNF138 | GRCh38.p7 | 18:32116696 | AGCTAGGACCATGGG[C/T]GCATGCCACCACATC | 51444 |
rs114759061 | snp | A/G/T | 0.00701346 | 0.0588029 | intron-variant | RNF138 | GRCh38.p7 | 18:32111733 | TTTTTTGTAATTAAT[A/G/T]TGTCACAATGTTTGG | 51444 |
rs114858550 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | RNF138 | GRCh38.p7 | 18:32110623 | TATATTTATAGGAGA[A/T]TGGATTAAATGTATA | 51444 |
rs114898997 | snp | A/T | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32107859 | ATATAACTACCCTTG[A/T]TTAAAGGGTACTTTT | 51444 |
rs114930746 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF138 | GRCh38.p7 | 18:32120731 | GATAGAAGGGAGAAC[A/G]TGTTTAAAAAGGGCA | 51444 |
rs115120276 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RNF138 | GRCh38.p7 | 18:32115769 | CACACGCACACACAC[A/G]CACGCACGCACACAC | 51444 |
rs115253792 | snp | A/G | 0.00795532 | 0.062565 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131783 | TTATGAAGTGTCTGC[A/G]GAGCAAGATTTTCAA | 51444 |
rs115423130 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RNF138 | GRCh38.p7 | 18:32114461 | AAAAATAATGATTAA[C/T]ATCCAGTTACCTATT | 51444 |
rs115442060 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RNF138 | GRCh38.p7 | 18:32126352 | TGGTTATTGTATGGA[C/T]CAAATGAGATAATAT | 51444 |
rs115448459 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32094437 | CGCTTTTGCTCTTTA[A/G]GGGAGATGAATGACA | 51444 |
rs115677333 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32110230 | ACTCCTTGCCTCAAG[C/G]TGTCCTCCTGCCTTG | 51444 |
rs115681281 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | RNF138 | GRCh38.p7 | 18:32122845 | TAACTAACTAACTAA[A/C]TAAATAAAATTGACC | 51444 |
rs115743519 | snp | C/T | 0.0217236 | 0.101931 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091361 | CAATTGTACAGATAA[C/T]TGCACTCCGGCCTGG | 51444 |
rs115799553 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | RNF138 | GRCh38.p7 | 18:32124196 | GTGATGCTTGATCCT[A/C]AGAATGTTTTCGAGT | 51444 |
rs115853219 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF138 | GRCh38.p7 | 18:32104707 | TTTGGACTAAACAAT[A/G]AAAATATACACAGCT | 51444 |
rs115873594 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32112065 | GAAAAGGCCAAAAAA[A/G]GCTGTGGTCATAGAT | 51444 |
rs116112404 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32115048 | GGTTTCTTCATTTCT[A/G]TGTTTTTCTTATTGT | 51444 |
rs116132001 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | RNF138 | GRCh38.p7 | 18:32115677 | TTGACCCTAGGAAAC[A/G]GAGGTTGCAGTGAGC | 51444 |
rs116133462 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | RNF138 | GRCh38.p7 | 18:32122982 | ATGGTAAAAGTGGAG[A/T]TGTTAAGTTGTTCTG | 51444 |
rs116246988 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF138 | GRCh38.p7 | 18:32106063 | CCCTTGTGCATTTTA[A/G]ATTTATTTCCATAAT | 51444 |
rs116377431 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | RNF138 | GRCh38.p7 | 18:32102097 | TGTGTTACCCAGAAT[G/T]GCCTCAAACTCCTGG | 51444 |
rs116403100 | snp | C/G | 0.013804 | 0.0819233 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092785 | CCCCGCCATGGCCGA[C/G]GACCTCTCTGCGGCC | 51444 |
rs116463302 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RNF138 | GRCh38.p7 | 18:32098298 | GGTGTGAGCCACTGC[A/G]CCCACAATATATTTC | 51444 |
rs116520179 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF138 | GRCh38.p7 | 18:32095023 | TCTCAAATCAACTTA[C/T]TGTACGTAGACAGTT | 51444 |
rs116529816 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RNF138 | GRCh38.p7 | 18:32120879 | CTGGGGGCGGTGGCT[C/T]ATGTCTGTAATCCCT | 51444 |
rs116557015 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF138 | GRCh38.p7 | 18:32108970 | ACTGCCCATGGTTTT[A/G]TGTATATAGGTTTGA | 51444 |
rs116620469 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32127309 | TAATGTAAAAATGAA[G/T]TCATAAAGCAAAATG | 51444 |
rs117484563 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | RNF138 | GRCh38.p7 | 18:32100843 | TGCCTGAGCTCAAGC[A/G]ATCTGCTCGCCTTGG | 51444 |
rs118156286 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129545 | ATTATTGTACACATT[A/T]AACACACAGTAGCAA | 51444 |
rs118163929 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32116129 | GTAAAGAAACTTGAC[A/T]AGTACTTTGCTTGGA | 51444 |
rs138002396 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32116762 | GTTTTTGGTGTTAAA[C/T]ACATTGAGATGGGGT | 51444 |
rs138018868 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097944 | TATGTGTATGTATAT[A/G]TGTGTGTGTGTGTGT | 51444 |
rs138041382 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32120162 | TAATATTACAAATAA[A/G]TATAATATTTACTAT | 51444 |
rs138106860 | in-del | -/CT | 0.14665 | 0.227637 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131305 | TGTTTAAAATTTCCC[-/CT]CTTTTTGTCAGTGCA | 51444 |
rs138119674 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | RNF138 | GRCh38.p7 | 18:32121996 | GCCTCAGCCTCCCGA[A/G]TAGTTGGGATTACAG | 51444 |
rs138150102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32127554 | ACATCATTCTTGTTA[A/C]ATGGTTTTTAAATTT | 51444 |
rs138150316 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32126131 | TGGGTGTGGTGGCAC[A/T]TGCCTTTAATCCCAG | 51444 |
rs138213559 | snp | A/C | 0.0422008 | 0.138995 | intron-variant | RNF138 | GRCh38.p7 | 18:32106523 | CTGGAAGATACTAGA[A/C]GTTGAAAAATTATTT | 51444 |
rs138310811 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF138 | GRCh38.p7 | 18:32097781 | GCCCGCCTTGGCCTC[C/T]GAAAGTGCTGGGATT | 51444 |
rs138324758 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | RNF138 | GRCh38.p7 | 18:32110803 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 51444 |
rs138376934 | in-del | -/TATG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097943 | ATATGTGTATGTATA[-/TATG]TGTGTGTGTGTGTGT | 51444 |
rs138418409 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF138 | GRCh38.p7 | 18:32094965 | GATTTGACCTCAAGA[C/G]TGTGGAAAATGTTGG | 51444 |
rs138592968 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RNF138 | GRCh38.p7 | 18:32121443 | GAGGTTGTGGTGAGC[C/T]GCGGTCGCGCCACTG | 51444 |
rs138672640 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32115387 | ATAATAGCCTTTTTA[C/G]CTGGTAGTTATCCTC | 51444 |
rs138693935 | snp | A/C | 0.00636936 | 0.0560724 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131701 | GCTGGTGCTATATGT[A/C]AGATTTAACTTTATA | 51444 |
rs138727351 | snp | A/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091422 | AAAATAAAATAAAAT[A/T]AAATTAAAAAAAACA | 51444 |
rs139005481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103573 | TTTGTCCTTCAAAGA[A/G]CACAATCAATAAACA | 51444 |
rs139005694 | in-del | -/TTAA | 0.0260105 | 0.111035 | intron-variant | RNF138 | GRCh38.p7 | 18:32107820 | CTGTGCCGGCCTTAT[-/TTAA]TTATTTTTATAACAG | 51444 |
rs139011117 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF138 | GRCh38.p7 | 18:32102746 | CAAGTGATTCTCCTG[C/T]CTCAGCCTCCTGAGT | 51444 |
rs139031895 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | RNF138 | GRCh38.p7 | 18:32106595 | ATTGAGATGGAGTCT[C/T]GCTCTGTCACACAGG | 51444 |
rs139135800 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | RNF138 | GRCh38.p7 | 18:32098209 | GCCAGGCTGGTTTTG[A/G]ACTCCAGGCTGGTTT | 51444 |
rs139173303 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | RNF138 | GRCh38.p7 | 18:32101468 | GAACTCCTGACCTCA[A/G]GTGATTTGCCTGCCT | 51444 |
rs139487284 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32128232 | AGCTGTAGGCTTCAT[A/G]TTATGGTTAAGAATT | 51444 |
rs139509794 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF138 | GRCh38.p7 | 18:32107391 | CTCCCAAAATGCTGG[A/G]ATTACAGGTGTGAGC | 51444 |
rs139603069 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32118564 | TGCCGGGCGCAGTGG[C/T]TCACGCCTGTAATCC | 51444 |
rs139613619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111584 | CCAGTTATCAGTCTT[A/T]CTCTCTGATAAATAC | 51444 |
rs139629608 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108193 | AATGCATACAGAAAC[A/G]TGTCCCTATCACAGA | 51444 |
rs139669975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111553 | GAGTGTAATTGTTCA[A/G]ATATTCCCATCTAGT | 51444 |
rs139738066 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant | RNF138 | GRCh38.p7 | 18:32124627 | TTTGAATAGTCTAAT[-/A]AATTATAACTTTTTT | 51444 |
rs139796065 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32096180 | ACCTAATGAATAATA[C/T]TAGACCTAGTAAATA | 51444 |
rs139803536 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RNF138 | GRCh38.p7 | 18:32096617 | CAGAAGGATAGGAAG[-/A]AAAACCAGGAATAAA | 51444 |
rs139815124 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF138 | GRCh38.p7 | 18:32099657 | TGATCTGCCCCGCCT[C/T]GGCCTCCCAAAGTGC | 51444 |
rs139934311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32122802 | GCACTCCAGCCTGGG[C/T]GACAGATTGAGACTC | 51444 |
rs140025617 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF138 | GRCh38.p7 | 18:32117705 | TCACTTTCATTCATA[C/T]CATTCAGAGTAGTAC | 51444 |
rs140050697 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32128162 | TGCATAGGGCATAAA[A/G]TTGATAGCAAATATA | 51444 |
rs140085127 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32132023 | ACCCCTTGTAGAAGC[A/G]TGACTTTTTAGCATA | 51444 |
rs140320541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32094135 | CAGGCTTGAAAGTTA[C/T]GTGTGTTTGCAAACA | 51444 |
rs140339792 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32125193 | GGCAGACAAGTAGAT[A/C/T]TAGTCAGGTAGATTG | 51444 |
rs140367287 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32096971 | TCCTGGGTGCAAACC[A/G]TCCTCCTGCCTCAGC | 51444 |
rs140426591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32106215 | TGTTAGTAGTCTGGC[A/G]ACAAGGTTGCACGAG | 51444 |
rs140642608 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF138 | GRCh38.p7 | 18:32110286 | GCATGAGCCACTACG[C/T]CCTGCCTAATGTTTT | 51444 |
rs140688756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112733 | GGTTAATTTTAAGGA[A/C]CATGTAGGAAAATCA | 51444 |
rs140724473 | in-del | -/G | 0.0170251 | 0.090679 | intron-variant | RNF138 | GRCh38.p7 | 18:32110549 | AAACTCAGGTTATGT[-/G]ATCTGTTACTGCACC | 51444 |
rs140752245 | in-del | -/G | 0.040671 | 0.13668 | intron-variant | RNF138 | GRCh38.p7 | 18:32099367 | GGTTGTACAGAGGAA[-/G]GAACAGTAAAATTGG | 51444 |
rs140788980 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32120856 | TATTTAAAACTGCAT[A/C]GTACTGGCTGGGGGC | 51444 |
rs140854540 | in-del | -/TGTGTGT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097971 | GTGTGTGTGTGTGTG[-/TGTGTGT]TATTTTTGTTTGTTT | 51444 |
rs140884859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32093892 | TACCAATTCCCAGGC[C/T]CCATTTCAAACTTAA | 51444 |
rs140890175 | snp | A/T | 0.0437281 | 0.141251 | upstream-variant-2KB, intron-variant | RNF138 | GRCh38.p7 | 18:32092365 | CGGAAAAGCAGTGAA[A/T]AGGGAGGCCTTGGGC | 51444 |
rs141055220 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090695 | CATTCTGATAGATAT[A/G]TAATAATGTAAACAG | 51444 |
rs141077935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32115865 | GGTTATCCATCGTTG[C/T]ATCACATGCCTTAGC | 51444 |
rs141085604 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32114201 | AATCCTTTTCAGTAA[C/T]GTATTTGCAAACTAC | 51444 |
rs141172429 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF138 | GRCh38.p7 | 18:32119378 | GTGTTGGGATCACAG[C/G]CATGAGCCTCTGTGG | 51444 |
rs141287170 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF138 | GRCh38.p7 | 18:32109990 | GGTAAATATTTTTAA[C/T]TGTTATTGTTTTTTG | 51444 |
rs141363245 | snp | A/C/T | 0.00755907 | 0.0610114 | intron-variant | RNF138 | GRCh38.p7 | 18:32117194 | GGCATGAACCACCCG[A/C/T]GCCCAGCCAGAAATT | 51444 |
rs141437350 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF138 | GRCh38.p7 | 18:32094642 | GGTGTCTAGGGCACA[A/T]TATAGATCTTCCACC | 51444 |
rs141536653 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | RNF138 | GRCh38.p7 | 18:32127985 | CTCGGGAGGCTGAGG[A/C]AGGAGAATGGGATGA | 51444 |
rs141604337 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106798 | ATCTTGATTTCCTGA[C/T]CTCGTGATCCGCCTG | 51444 |
rs141836146 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32123159 | AATTCTTGAGTCTAC[C/T]GTAGCATTTAAAACC | 51444 |
rs141859704 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130522 | TTGCTGACATTCCAT[A/G]CTAATATACATTGTT | 51444 |
rs141876687 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091356 | ATTATCAATTGTACA[C/G]ATAATTGCACTCCGG | 51444 |
rs141920420 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF138 | GRCh38.p7 | 18:32102307 | CCCAGGTTCACACCA[C/T]TCTCCTGCCTCAGCC | 51444 |
rs141984958 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | RNF138 | GRCh38.p7 | 18:32122014 | GTTGGGATTACAGGC[G/T]CCCGTCACCACACCC | 51444 |
rs142266363 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | RNF138 | GRCh38.p7 | 18:32106710 | GCTGGGACTACAGGC[A/G]CCCGTCACCATGCCT | 51444 |
rs142338609 | in-del | -/TA | 0.134119 | 0.221521 | intron-variant | RNF138 | GRCh38.p7 | 18:32094780 | GTAATAGCTGCTAAC[-/TA]TATATATATATATAT | 51444 |
rs142375519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101038 | TTTAGGAAGTGATAT[G/T]GTTGCTGATATCTAA | 51444 |
rs142459990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32119140 | TTCATTGAGGAGTCA[G/T]TTCTTTGTCTACTGA | 51444 |
rs142526036 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32095956 | GATAATTTCCTAGAT[G/T]AAGTAATGCCTTAGG | 51444 |
rs142622158 | snp | G/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090040 | CGCTGGAGGCCAGGA[G/T]TTCGAGACTAGCCTG | 51444 |
rs142630960 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RNF138 | GRCh38.p7 | 18:32100097 | TTGCTTTAGCAAATA[A/T]TAGGACTGCCTAATA | 51444 |
rs142682243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32126260 | AAGAAAAACTAAGGA[G/T]ACAATTTAAAGTAAA | 51444 |
rs142724294 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107514 | TTAATTTAGTTTTTT[A/G]TTTGTTTGTTTGTTT | 51444 |
rs142786839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109361 | CCAGGCTGGTCTTGT[A/G]AGCTTAAGCCATTTG | 51444 |
rs142823185 | snp | C/G | 0.0482946 | 0.147699 | intron-variant | RNF138 | GRCh38.p7 | 18:32107768 | GTTATCCACCCGCCT[C/G]AGCCTCCCAAAGTGC | 51444 |
rs142877097 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32122550 | CACATTGGGCCAGGC[A/G]CGGTGGCTCACACCT | 51444 |
rs143017542 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32111022 | CCTGACCACGTGATC[C/T]GCCTGCTTCAGCGTC | 51444 |
rs143080355 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RNF138 | GRCh38.p7 | 18:32124381 | ACTACAGAATATTAA[A/C]AATTTTCAAGGGACA | 51444 |
rs143163697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32099705 | GCCACTGCACCCGGC[C/T]ATTCTTTGTACCTGT | 51444 |
rs143501567 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090359 | ACTGCTATTAGCTGC[C/T]CCTCTCGTCACGTGC | 51444 |
rs143534442 | snp | C/T | 0.000307953 | 0.0124049 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111874 | CTTAGACCTTGAAAA[C/T]ATAATGAGGAAGTTT | 51444 |
rs143585179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32118394 | CAAAAATTAGCCAGG[C/T]GTGGTGGCACACACC | 51444 |
rs143605454 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF138 | GRCh38.p7 | 18:32094554 | TCACAGGCATGTGTG[A/G]GATATGCCATCCTCA | 51444 |
rs143628440 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32111563 | GTTCAAATATTCCCA[A/T]CTAGTCCAGTTATCA | 51444 |
rs143664464 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF138 | GRCh38.p7 | 18:32116937 | AGACAGAGTTTTGCT[C/T]GTCTCCCAGGCTGGA | 51444 |
rs143693026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101946 | CAGGGGCATAATCAC[G/T]GCTTACTGCAGCCTC | 51444 |
rs143705121 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32112443 | TAATCCCAGCACTTA[C/T]GGGAGGCCAAGGTGG | 51444 |
rs143736933 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129489 | GAATTTTTCATTATT[A/T]TGTTGCTTTTGAAAT | 51444 |
rs143757567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32113143 | AGTGGCACAATCTCG[C/G]CTCACTGCAGCTTTG | 51444 |
rs143790117 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF138 | GRCh38.p7 | 18:32097818 | ATGAGCCACTATCCT[C/T]GGCCTAATTAATTAA | 51444 |
rs143919793 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | RNF138 | GRCh38.p7 | 18:32103955 | GGGCGACAGAGCAAG[A/G]CTCCGTCTCAGAAAA | 51444 |
rs143925147 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | RNF138 | GRCh38.p7 | 18:32095044 | GTAGACAGTTCTGCC[C/T]GAACAATGAATTAAA | 51444 |
rs143986229 | in-del | -/AA | 0.0640965 | 0.167152 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091719 | GGTAGGGCAAATAGT[-/AA]AGACTAAATCTTGAA | 51444 |
rs144017581 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | RNF138 | GRCh38.p7 | 18:32116987 | GCTCACTACAACATC[A/G]ACCTCCCAGGTTCAA | 51444 |
rs144029063 | snp | A/G | 0.0283406 | 0.115616 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091942 | TCTCCTGGCTCCTCC[A/G]CCCAGATCCCCGGCG | 51444 |
rs144230350 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090215 | CATTCCACTGCACCC[C/T]AGCCTGGGTGACAGA | 51444 |
rs144402321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32104277 | TTCGGCGTCCCAAAG[A/G]GCTGAGATTACATGC | 51444 |
rs144757982 | snp | A/G | 0.0111196 | 0.0737302 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091733 | TAAAGACTAAATCTT[A/G]AACATTGACGAAAAC | 51444 |
rs144763494 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090743 | TGACATCTGCATAAC[A/C]CCTAACAATGCCAAT | 51444 |
rs144824922 | in-del | -/G | 0.127254 | 0.217792 | intron-variant | RNF138 | GRCh38.p7 | 18:32116737 | TTGATTTTTTGGGGT[-/G]GGGGGGGTGGTTTTT | 51444 |
rs144846953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32127376 | TTAATTAGGTGAAAA[C/T]CTGTTTTATTAATTA | 51444 |
rs144863817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32095737 | TAGAATAACATTACT[A/G]AAATATAAACTCCCG | 51444 |
rs144967702 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | RNF138 | GRCh38.p7 | 18:32093548 | ACTGACAGGATTTTC[A/G]GGCATTGAAATGAGC | 51444 |
rs145012986 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128092 | CTCAAAAAAGAAAAG[A/T]AGGTGATCTAATTAT | 51444 |
rs145039241 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32110193 | AGACAGGGTCTTGCT[A/G]TGTTGCCCAGGCTGG | 51444 |
rs145045010 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF138 | GRCh38.p7 | 18:32108866 | TTTAATTTTTTTACA[A/G]GAGCAAAGTCTCACT | 51444 |
rs145101614 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32106534 | TAGAAGTTGAAAAAT[C/T]ATTTTTTATTTTATT | 51444 |
rs145126805 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | RNF138 | GRCh38.p7 | 18:32097488 | TTTAAAACAATTTTA[A/C]ATTAATTATTTATTT | 51444 |
rs145171612 | in-del | -/GTTTTT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094294 | CCCTTACTGTGGCTG[-/GTTTTT]TTTTCTTGATACCAA | 51444 |
rs145207302 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32112039 | AAGGTATTTAGACTG[C/G]GAATTGGATAGAAAA | 51444 |
rs145282959 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32105576 | TGTAGAATCTCTGCT[A/G]TGTGCTATACATGAT | 51444 |
rs145303768 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32108207 | CGTGTCCCTATCACA[G/T]ATATCCAGCTCAGTG | 51444 |
rs145533936 | in-del | -/T | 0.0741063 | 0.177655 | intron-variant | RNF138 | GRCh38.p7 | 18:32102640 | TAATTTGGGATTTTC[-/T]TTTTTTTTTTGAGAA | 51444 |
rs145622518 | in-del | -/T | 0.0274168 | 0.113828 | intron-variant | RNF138 | GRCh38.p7 | 18:32111716 | AGATGAAGAGAGTAA[-/T]TTTTTTTGTAATTAA | 51444 |
rs145673372 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32128208 | GAGTAGTTTTATAAC[A/G]ATTGAATAAGCTGTA | 51444 |
rs145896976 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32110331 | ATTGGTAATGACTTC[C/T]AGTGCTGCTTTAATG | 51444 |
rs146035926 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32093104 | AGCCCCCTCAGCCCA[A/G]GCTCCCGCTCTCCCG | 51444 |
rs146040633 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098928 | GATTTTTTTTTTTTT[-/T]GAAGTTTTTTTGGGG | 51444 |
rs146141737 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32099606 | GATGGTGTTGCACCA[C/T]GTTGGTCAGGCTGGT | 51444 |
rs146176215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103170 | AAAAATTCATTCAGC[A/G]TTTGTTTATTTTTCA | 51444 |
rs146226099 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF138 | GRCh38.p7 | 18:32099853 | AGCCTACTAATATAT[C/T]GTTTCACATATGAGA | 51444 |
rs146344046 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32118563 | ATGCCGGGCGCAGTG[A/G]CTCACGCCTGTAATC | 51444 |
rs146348183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101090 | GTGGAGGGCTGTGCT[C/T]GTGCATAGAACATTC | 51444 |
rs146430117 | in-del | -/AG | 0.442926 | 0.158996 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130917 | AACAGCTCCTTTTTA[-/AG]AGACTTTTGACCATA | 51444 |
rs146489940 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128663 | GTTATGATTAACTTC[A/C]GTTTTATTTTTCATT | 51444 |
rs146518451 | in-del | -/T | 0.0494327 | 0.149241 | intron-variant | RNF138 | GRCh38.p7 | 18:32097065 | ACATGTTAAGACAAA[-/T]TAATATGAAAGTTGA | 51444 |
rs146555305 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | RNF138 | GRCh38.p7 | 18:32097876 | TCGGGCTATATATAT[A/G]TATATATGTGTATGT | 51444 |
rs146681474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096235 | TCACATTTCATTTTT[A/G]GAAAGTTTACCTTCA | 51444 |
rs146697467 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107518 | TTTAGTTTTTTGTTT[G/T]TTTGTTTGTTTGTTT | 51444 |
rs146731021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32094043 | TGATCCTCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 51444 |
rs146803080 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32112622 | GGGCGGCAGAGGTTG[C/T]GGTGAGCTGAGATTG | 51444 |
rs146852116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32110197 | AGGGTCTTGCTATGT[G/T]GCCCAGGCTGGTCTT | 51444 |
rs146926956 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF138 | GRCh38.p7 | 18:32119811 | GTAAAACCTTATAGT[C/T]TTTGTTGCTATAAAA | 51444 |
rs146970479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32116208 | CACTTTTACCAGTAA[C/T]ATCCCAACCTGCATT | 51444 |
rs147262300 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF138 | GRCh38.p7 | 18:32095073 | AAAGAATAGGCAGAG[A/G]GAGAAAAAAAGTTTA | 51444 |
rs147292935 | snp | C/T | 0.0182019 | 0.0936463 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092155 | GCCGGACAGGAAGCT[C/T]GAGGAAAGCGCTGGG | 51444 |
rs147347031 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097977 | GTGTGTGTGTGTGTG[G/T]TATTTTTGTTTGTTT | 51444 |
rs147409026 | in-del | -/ATTACAGGC | 0.0205511 | 0.0992634 | intron-variant | RNF138 | GRCh38.p7 | 18:32117173 | TCCCAAAGTGATGGG[-/ATTACAGGC]ATGAACCACCCGCGC | 51444 |
rs147473089 | snp | C/G | 0.0023933 | 0.0345097 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131787 | GAAGTGTCTGCGGAG[C/G]AAGATTTTCAAGCCC | 51444 |
rs147516208 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | RNF138 | GRCh38.p7 | 18:32128003 | GAGAATGGGATGAAC[C/T]CGGGAGGCAGAGCTT | 51444 |
rs147566879 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32124163 | TCCCTTCCTGAAATT[A/C]AGAAGTATTAAAACT | 51444 |
rs147732866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32128229 | ATAAGCTGTAGGCTT[C/T]ATGTTATGGTTAAGA | 51444 |
rs147837226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32100946 | GCTCAGAAAAATGGT[A/G]TAATTACAAATGTAT | 51444 |
rs147860563 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF138 | GRCh38.p7 | 18:32105068 | TAAAAATATAAAAAT[A/G]CAAAATGAAAATTAA | 51444 |
rs147881372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32105700 | CTTAAGACTGCAAAA[C/G]CATAAACCATAATTT | 51444 |
rs147956739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32119314 | TATGTTTCCCAGGCC[C/T]GTCTCAAACTCTGGG | 51444 |
rs147966169 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32123112 | GGGCATAACCTTATA[C/T]CATGTCCTAGTTTGA | 51444 |
rs147983842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32106765 | GAGACAGGGTTTCAC[C/T]GTGTTAGAGCCAGGA | 51444 |
rs147994559 | snp | C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090379 | TCGTCACGTGCTCTT[C/T]CTCCTTCCAGGAAAT | 51444 |
rs148087296 | in-del | -/TAAC | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32112977 | TTTGAAGGAAGTGTT[-/TAAC]TGACAGGGCAATGAC | 51444 |
rs148143401 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF138 | GRCh38.p7 | 18:32102000 | TCCCACCTCAGCCTC[C/T]CAAGTAGCTGGGACT | 51444 |
rs148227099 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | RNF138 | GRCh38.p7 | 18:32111034 | ATCCGCCTGCTTCAG[C/T]GTCCCAAAGTGCTGG | 51444 |
rs148271161 | snp | G/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130114 | TATATATACACATAT[G/T]TGTGTATGCAGTTTG | 51444 |
rs148348977 | in-del | -/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101214 | ACCTCTTATAGGTTT[-/C]TTTTTTTTTTTTTTT | 51444 |
rs148520426 | snp | G/T | 0.0611083 | 0.163768 | intron-variant | RNF138 | GRCh38.p7 | 18:32109193 | AGGTCTCACTCTGTT[G/T]CTCAGGCTGAAGTGC | 51444 |
rs148582385 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF138 | GRCh38.p7 | 18:32095802 | TTGAATGCTCTTTGT[C/T]TGGTGCAGGGACTAC | 51444 |
rs148608895 | in-del | -/G | 0.0159621 | 0.0878991 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129213 | CATCTCTGCATCTTT[-/G]TACCTGCAAGTGCCA | 51444 |
rs148740449 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | RNF138 | GRCh38.p7 | 18:32127904 | GCTAACACGGTGAAA[C/G]CCCGTCTTTACTAAA | 51444 |
rs148774414 | in-del | -/AGC | | | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131807 | TTTTCAAGCCCTGTT[-/AGC]AGCTAGGCAGAAAGC | 51444 |
rs148814350 | snp | C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090325 | CATTTTATAAGTGAA[C/T]GTGAAAAGCACCTGA | 51444 |
rs148844017 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32128468 | GCTTGAGCCCAGGAG[A/G]TGGAGGTTGCAGTGA | 51444 |
rs148961195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32101648 | CATATTATGTACGCA[A/G]TAAGTGTTAACTGCT | 51444 |
rs148981834 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128094 | CAAAAAAGAAAAGTA[A/G]GTGATCTAATTATTT | 51444 |
rs149002606 | in-del | -/TGTT | 0.109523 | 0.2068 | intron-variant | RNF138 | GRCh38.p7 | 18:32128886 | TGTGATGATCCTCTC[-/TGTT]TGTTTGTTATTCTTG | 51444 |
rs149022051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32124301 | TATTTATTAGAGATA[C/T]GATATTGATGGAAGT | 51444 |
rs149285071 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32121463 | TCGCGCCACTGCATT[C/G]CAGCCGGGGCAATAA | 51444 |
rs149299151 | snp | A/G | 6.67646e-05 | 0.00577736 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111799 | GAGGGAAAGCGGAGC[A/G]CATTGTCCCCTATGT | 51444 |
rs149309856 | in-del | -/A | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106114 | TCCCTCTCTTCTTTT[-/A]AAAAAATTTTAGGGT | 51444 |
rs149390491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32095281 | TTGGAGCAACCCTCC[C/T]GCCTCAGCCTCTCAA | 51444 |
rs149467672 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | RNF138 | GRCh38.p7 | 18:32110912 | CAGCCTCCCGGGTAG[C/G]TGAAACTACAGGCGC | 51444 |
rs149562419 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RNF138 | GRCh38.p7 | 18:32127631 | ATATGTAAAATTTAG[A/G]TGCGCTTTATTGCTT | 51444 |
rs149664013 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32128311 | GGGAGGCCGAGGCGG[A/G]TGGATCACCTGAGGT | 51444 |
rs149747254 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | RNF138 | GRCh38.p7 | 18:32100771 | GTGAGCCCCCGCGCC[C/T]GGCCTGTATTTTTTG | 51444 |
rs149799964 | in-del | -/TTTGTTTG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107511 | ATCTTAATTTAGTTT[-/TTTGTTTG]TTTGTTTGTTTGTTT | 51444 |
rs149823341 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32122864 | ATAAAATTGACCACA[C/T]TGATCAAATTCTGTA | 51444 |
rs149876783 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32093498 | ACTATGTGTTAGAGG[A/G]ATCTAGAATGAGTTT | 51444 |
rs149908906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103658 | TTAGACAAGAGTACA[G/T]GTTGAGCTTTTGAAA | 51444 |
rs149991153 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RNF138 | GRCh38.p7 | 18:32111610 | AATACATATACAGTT[A/G]CTAAACTTCTGAGAT | 51444 |
rs150104067 | in-del | -/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116515 | CAAAGGAAGGAAAAG[-/C]TTTTTTTTTTTTTTT | 51444 |
rs150187495 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131224 | TGTGTGTCTCACATA[A/T]CAGCTTTTTCATAAG | 51444 |
rs150262636 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32114818 | TAACTTAACCGCCCT[C/T]AAGCACTTCATGTTG | 51444 |
rs150347779 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF138 | GRCh38.p7 | 18:32097071 | TAAGACAAATTAATA[C/T]GAAAGTTGAGCAGGT | 51444 |
rs150398450 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF138 | GRCh38.p7 | 18:32094952 | AGGTTTATAATTTGA[C/T]TTGACCTCAAGACTG | 51444 |
rs150430778 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32106271 | ATAAGCCCTATAAGT[C/T]TTAGTGTGCGGGTAT | 51444 |
rs150547527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32106809 | CTGACCTCGTGATCC[A/G]CCTGCCTCGGCCTCC | 51444 |
rs150626339 | in-del | -/AAAC | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104557 | GATTAAAAACAAGAG[-/AAAC]AATAAGAGTACAGGG | 51444 |
rs150640792 | in-del | -/GAAATG | 0.00197225 | 0.0313406 | intron-variant | RNF138 | GRCh38.p7 | 18:32113901 | AGAATTTTCATAATT[-/GAAATG]GAAATTGTTTTGGGA | 51444 |
rs150787039 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117555 | TCACTAATTCATACT[A/G]TTTATTATACGTTCT | 51444 |
rs150789136 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091399 | AGTGAGTACCTGTCT[C/T]AAAAAATAAAATAAA | 51444 |
rs150843987 | in-del | -/ATT | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32127672 | ATAAAGTAATTCTAG[-/ATT]ATTATTAAATTCTCA | 51444 |
rs150872687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098959 | AATGATCTCGATTAT[C/T]GACTCGGAAAATAGA | 51444 |
rs150910685 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129488 | TGAATTTTTCATTAT[G/T]ATGTTGCTTTTGAAA | 51444 |
rs150937871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096018 | GCCAGAGTCAAGGAG[G/T]GTACAGAGGATGAAT | 51444 |
rs150989216 | snp | C/G | 0.0614824 | 0.164198 | intron-variant | RNF138 | GRCh38.p7 | 18:32100516 | GTTTTGCTCTTGTTG[C/G]CCAGGCTGGAGTGCA | 51444 |
rs151072654 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32109616 | AGTTTTGCTGGGCAC[C/T]ATGGCTCACGCCTGT | 51444 |
rs151168438 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32124575 | GAACCTCTGTAATGC[A/C]TCATTTCCTGAATAC | 51444 |
rs151315163 | snp | C/G/T | 0.00487475 | 0.0491686 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092872 | GCCCGTGCGGACCAC[C/G/T]GCCTGTCAGCACGTG | 51444 |
rs180693550 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091392 | GAGACAGAGTGAGTA[C/T]CTGTCTCAAAAAATA | 51444 |
rs180850310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32124558 | CTGTAAACTGAGATT[A/G]GGAACCTCTGTAATG | 51444 |
rs180917338 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095447 | AAAGTGCTGGGATGA[C/T]AGGCGTGAGGCATGG | 51444 |
rs180936722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32114941 | ATTGCCTAGTCTGAA[A/G]AAACTTCAGGTTCTC | 51444 |
rs180971137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32105462 | AGAAATAGTTCCACA[C/T]GTTTTGGAACTTTTT | 51444 |
rs181114416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32114530 | ATCTCTATGTGAGCT[C/T]CTGCCCATTTGAACC | 51444 |
rs181179441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32123839 | TGTATTTTTAGTAGA[A/C]ACAGGGTTTCACCAT | 51444 |
rs181237231 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095977 | ATGCCTTAGGTCAGC[A/G]TTTGTATTCAGTGTT | 51444 |
rs181320855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32128552 | CAAAAAATTTCTTAC[C/T]CAACTCATAATTCAA | 51444 |
rs181453978 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32105151 | GGCTGGAGTGCAGTG[A/G]CACCATCTTGGCTCA | 51444 |
rs181468451 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32096255 | GTTTACCTTCATAGC[A/C]GGGTTTTCAGCTTGG | 51444 |
rs181616463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32120189 | CTATAGTTTTTTAGC[A/G]TAGATCTTTTAGTTT | 51444 |
rs181671570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32100110 | TATTAGGACTGCCTA[A/G]TAGGTGCCTAGCACT | 51444 |
rs181751039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32127888 | GATTGAGACCATCCT[G/T]GCTAACACGGTGAAA | 51444 |
rs181842297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32111385 | GGAGATCCAGTGTGC[A/G]TTAATTTGTTGGCCT | 51444 |
rs181842542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32118798 | CGTGCCACTAACACT[C/T]CAGCCTGGGCGACAG | 51444 |
rs181903948 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF138 | GRCh38.p7 | 18:32100561 | GCTCACTGCAACCTC[C/T]GTCTCCCGGGTTTAA | 51444 |
rs182041678 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090254 | CTGTCTCAAAAGAAA[A/G]AAGAAAAAAAGTGAG | 51444 |
rs182060317 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF138 | GRCh38.p7 | 18:32123100 | CTGCACTTTGGAGGG[C/T]ATAACCTTATACCAT | 51444 |
rs182083114 | snp | C/T | | | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091731 | AGTAAAGACTAAATC[C/T]TGAACATTGACGAAA | 51444 |
rs182147142 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNF138 | GRCh38.p7 | 18:32092582 | GGGGTCGCCTCTTGC[C/T]CGGCGCGTGCGGCAG | 51444 |
rs182265459 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129454 | CCTGTTGTACTTTAT[C/T]TTTTTGTAATATTAT | 51444 |
rs182289669 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32115614 | GCTGGACGTGGTGGC[A/G]CGTGCCTATAGTCCC | 51444 |
rs182348849 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32110417 | CATTTTATACTTGTT[A/G]TCTATTTTAATCCTC | 51444 |
rs182403477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096713 | CAGAGGCCTTAGAGT[A/G]GTCAGATGTAATTTT | 51444 |
rs182510968 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RNF138 | GRCh38.p7 | 18:32106190 | ATTTTTATTTGGATT[G/T]TTTGGGTTTTGTTAG | 51444 |
rs182561794 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32115993 | TTCAGATGTCACTTA[C/G]TAATTGTATTACATT | 51444 |
rs182657446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101403 | TTTGTGTATATATAT[A/G]TATTTTTAAATTAGA | 51444 |
rs182712384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32107414 | GTGTGAGCCACTGTA[C/T]CTGGCCCACTTTCCT | 51444 |
rs182776578 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32098132 | GTTGGGATTACAGGC[A/G]TGCACCATCACGCCC | 51444 |
rs182784194 | snp | A/G | | | utr-variant-3-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32131025 | TCTGGGATTTGCAAA[A/G]TTTAATACATCCAAT | 51444 |
rs182791439 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF138 | GRCh38.p7 | 18:32112444 | AATCCCAGCACTTAT[A/G]GGAGGCCAAGGTGGG | 51444 |
rs182846723 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32116965 | GGAGTGCAGTGGTGC[A/C/G]ATCTCAGCTCACTAC | 51444 |
rs182871795 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32121797 | GCACTCTCCATAATT[G/T]GACTTTATTTTAAAG | 51444 |
rs182995440 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097586 | CCTCCTGGATTTAAG[C/T]GATTCTCCTGCCTCG | 51444 |
rs182996841 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32102581 | ATTTGAAGAGTTTGT[A/G]TTGTACAGTTTGTCA | 51444 |
rs183114492 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121575 | TCCTCCCCAATGATA[C/T]TATAGTTCTATAAAC | 51444 |
rs183123222 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF138 | GRCh38.p7 | 18:32125722 | GGATTGCTTGAGCCC[A/G]GGAGTTCGAGACTAG | 51444 |
rs183142727 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32120258 | TAAGGTTTCCCCATT[A/C]ATAGTTTTACTCAAA | 51444 |
rs183357442 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091974 | TCCCGCGTTCGGTGA[C/T]GGCCGGGTAGGCTGT | 51444 |
rs183388126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32117422 | AGGAGAGAGGAGGAA[A/G]TAGATAACAGAACCT | 51444 |
rs183409478 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097940 | TGTATATGTGTATGT[A/G]TATATGTGTGTGTGT | 51444 |
rs183429596 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130356 | TATTCTCAAATATAA[G/T]GTGTGACCGTGATAT | 51444 |
rs183536960 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF138 | GRCh38.p7 | 18:32106702 | CTTGAGTAGCTGGGA[C/T]TACAGGCGCCCGTCA | 51444 |
rs183544777 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095663 | TTAATTGCCATTTCA[A/G]TGACAGGAAAGGATT | 51444 |
rs183757228 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32126091 | AGTTTTTAAGATGTA[A/C]TTCATTTAAACGTAA | 51444 |
rs183759739 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RNF138 | GRCh38.p7 | 18:32098590 | GGGCGCAGTGGCTCA[A/C]GCCTGTCATCCCAGC | 51444 |
rs183769035 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090606 | ATATTTCTAATCATT[A/C]CATTTCCTATCCTCA | 51444 |
rs183788907 | snp | A/C/G/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32110471 | TACTTTTATTATTTC[A/C/G/T]TGAGTGAGGAAACTG | 51444 |
rs183832387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117895 | TGTTTTCTTTAGCCA[C/T]AGGAAGTGGGGAGGA | 51444 |
rs183888869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103532 | TTTGTGTACCTGATA[C/T]TCAAGGCACCAAGAA | 51444 |
rs184033327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32124942 | AAGTAGTTGATTTAT[A/G]TTTGGTTGGGGCATT | 51444 |
rs184067015 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114627 | ATCATCACCCATGCA[C/T]GTATCCCTAAACAAT | 51444 |
rs184193835 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32108639 | ATGAACTTTCTAGCA[A/C]ATTTTTTCTGATTAT | 51444 |
rs184303747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32114474 | AACATCCAGTTACCT[A/G]TTAACCCAGGTCAAG | 51444 |
rs184344125 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32104542 | TTGTCATAATTTGTC[A/G/T]ATTAAAAACAAGAGA | 51444 |
rs184428655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32118759 | CCTTGAACCCGGGAG[A/G]CCAAGGTTGCAGTGA | 51444 |
rs184692695 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128004 | AGAATGGGATGAACC[C/T]GGGAGGCAGAGCTTG | 51444 |
rs184697805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32104971 | AGATAGCACAACCCT[A/G]TCAGATATAATGAGA | 51444 |
rs184730624 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32094739 | GGTAGATAAAAGGGA[G/T]GGAGGAGAGCAAGGT | 51444 |
rs184740236 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32122805 | CTCCAGCCTGGGCGA[C/T]AGATTGAGACTCCAG | 51444 |
rs184807618 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF138 | GRCh38.p7 | 18:32099160 | AGACCTTTTTTGGTT[A/G]TAGGGTAATGCCCTG | 51444 |
rs184878721 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF138 | GRCh38.p7 | 18:32122331 | AAGTAAACAGAAAAG[A/G]AAGATCAGCTGCTAA | 51444 |
rs185012251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32129024 | GTAATGTGTGTCAAG[A/T]TGTGTAATGTGTATC | 51444 |
rs185227620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32123160 | ATTCTTGAGTCTACC[A/G]TAGCATTTAAAACCT | 51444 |
rs185253210 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32124642 | TAATTATAACTTTTT[A/T]AAAAAATGTATAGTG | 51444 |
rs185276402 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF138 | GRCh38.p7 | 18:32106235 | GGTTGCACGAGTGGT[C/T]TATTCCAACCATTTT | 51444 |
rs185410102 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32113142 | CAGTGGCACAATCTC[A/G]GCTCACTGCAGCTTT | 51444 |
rs185434181 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32093589 | GTTTTACCTTTCTGC[G/T]TACTTATTACTTGAT | 51444 |
rs185523972 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091663 | AAAATCCCGTAACAA[A/G]TATTTGTTTATAACA | 51444 |
rs185527218 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131496 | CAAATTACAGTTTTA[C/T]TGTTAAAACAGAGTC | 51444 |
rs185531905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111084 | CGTGCCCGGCAAAGC[C/T]GGAAGTATTCTTAAG | 51444 |
rs185642096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32127126 | AAGTAAAATTGGTAC[A/G]ACATATGGAGGATGT | 51444 |
rs185749552 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116584 | TTAGACAGGGTCTTG[C/T]TCTGTCATCCAGCCT | 51444 |
rs185999406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32120884 | GGCGGTGGCTCATGT[C/T]TGTAATCCCTGTACT | 51444 |
rs186012431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32105603 | TGATAATATTTCCAG[A/G]TGGATTGAAAACTTT | 51444 |
rs186012946 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100152 | GGGATATTGTAAAGA[A/G]CAAATAGATAGGATC | 51444 |
rs186024361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32115739 | GACAGAGTCAGACTC[C/T]GTCTAAAACACACAC | 51444 |
rs186073986 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100673 | AGAGACGGGGGTTTC[A/T]CCATGTTGGTCAGGC | 51444 |
rs186285187 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32100814 | TTCACCATGTTGGCC[A/G]GGCTGGTCTCGAATG | 51444 |
rs186406640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32124043 | TAGAAAATGCAGTTA[C/T]TGCTTTTAAGAATCA | 51444 |
rs186447036 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32101472 | TCCTGACCTCAAGTG[A/G]TTTGCCTGCCTCACT | 51444 |
rs186487948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096312 | GTCATTCATTGATGT[A/G]TCAGGGAGAGAAATG | 51444 |
rs186497602 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32118905 | TTGTTTAGTCTTTGG[C/T]TGGTTTTGTATGGTG | 51444 |
rs186681147 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131039 | AGTTTAATACATCCA[A/G]TATGTCAAGTTAAAC | 51444 |
rs186682816 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091764 | TTCCTGAAAGGCCCA[A/G]TGTATTTGACAGGAG | 51444 |
rs186685808 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF138 | GRCh38.p7 | 18:32112670 | CTGGGCAACAAGAGC[A/G]AAACGCTGTCTAAAA | 51444 |
rs186762382 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32107918 | CCCAGATTGGGGCGC[A/G]ATCTCGGCTCACTGC | 51444 |
rs186906025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111418 | GATTACACAGCTACT[A/C]AATGGCAGAGCCAGG | 51444 |
rs186930148 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | RNF138 | GRCh38.p7 | 18:32126242 | CTAGTTTTAAGAAAA[G/T]AAAAGAAAAACTAAG | 51444 |
rs186977040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32120235 | CCATGTCAGTATTAC[C/T]CTGAATTTAAGGTTT | 51444 |
rs186988337 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32115018 | TGCTCTTATAGTTTT[A/T]TTTTAGTCCTTCTGG | 51444 |
rs187027621 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF138 | GRCh38.p7 | 18:32108914 | CTCAAGTAATCCTCC[C/T]GCCTTGGCCTCCCAA | 51444 |
rs187155539 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF138 | GRCh38.p7 | 18:32096171 | AATTAGATAACCTAA[C/T]GAATAATACTAGACC | 51444 |
rs187229716 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32105314 | CAGGCTGGTCTTGAA[A/C]TCCTGACCTCAATTG | 51444 |
rs187275743 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RNF138 | GRCh38.p7 | 18:32117701 | TGTGTCACTTTCATT[C/G]ATATCATTCAGAGTA | 51444 |
rs187327316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32103397 | GAAATCTCACTATGT[C/T]GCCCAGGCTGGTCTT | 51444 |
rs187552275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096860 | ACCTCCCAAGTAGCT[A/G]GCTGGGACTACAGGC | 51444 |
rs187661874 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130400 | CTACCAACCACTGTT[C/T]CACTACTTTTTAGTT | 51444 |
rs187668151 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32111976 | TCTACTCTGAAATTC[G/T]TATTTGAATTTTCTT | 51444 |
rs187700507 | snp | A/G | 0.0111196 | 0.0737302 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092072 | GCTCCGGCCCCGTTA[A/G]GGGCCGATAAGCACA | 51444 |
rs187746740 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116982 | TCTCAGCTCACTACA[A/G]CATCGACCTCCCAGG | 51444 |
rs187791941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121606 | CTATTAGAAGTTGTT[A/G]ACAGTATTTTTAAAG | 51444 |
rs187859375 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32098528 | TAAAATAATTTTCTT[C/G]TTTCCTAAAATCTGT | 51444 |
rs188004414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125890 | GGGTTCAGTTATGCT[C/T]AAATAGACAAATACA | 51444 |
rs188086506 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RNF138 | GRCh38.p7 | 18:32097600 | GCGATTCTCCTGCCT[C/T]GTCCTCCTGAGTAGC | 51444 |
rs188154154 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090711 | TAATAATGTAAACAG[A/G]TTGAGAGCAAAGTTC | 51444 |
rs188163098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32110525 | GTTTAAAAGTGCTGC[A/G]TAGTTAGGAAACTCA | 51444 |
rs188350516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32094458 | ATGAATGACATCTTG[A/T]TATTTTGTGCAACAA | 51444 |
rs188353136 | snp | C/T | 0.000196444 | 0.00990876 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092675 | ATCCTGATGCGATCC[C/T]CCTCCCCCCTCCGGG | 51444 |
rs188529029 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128271 | ATCTGGGCATGATGG[A/C]TCATGCCTGTCATCC | 51444 |
rs188530647 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF138 | GRCh38.p7 | 18:32122029 | GCCCGTCACCACACC[C/T]GGCTAATTTTTGTAT | 51444 |
rs188564988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32124973 | ATCAGTAAGGTAGAT[A/T]TTTGTCAACAAAGGA | 51444 |
rs188787840 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131541 | TTGCTTTATTTTTCA[A/G]TTAAAAGTGGTTTTC | 51444 |
rs188864284 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF138 | GRCh38.p7 | 18:32107213 | GCAACCTCTGCCTCC[C/T]GGGTTTAAGCAGTTC | 51444 |
rs188891731 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RNF138 | GRCh38.p7 | 18:32104052 | AGAGTCTAGTTCTGT[C/T]GCCCATGCCAGAGTG | 51444 |
rs188922125 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32120036 | TTTGTCTGCTTCTTT[C/T]AAACCTAATGTTCTA | 51444 |
rs189034248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32114682 | GTAGTAAGCACATAC[A/G]TAACTGTAAGGAAAG | 51444 |
rs189067580 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RNF138 | GRCh38.p7 | 18:32104991 | ATATAATGAGATATT[A/T]TGAAACAATAGTAAT | 51444 |
rs189074629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32114516 | TTCAAAACTTCAGGA[C/T]CTCTATGTGAGCTCC | 51444 |
rs189076122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32113178 | CCCAGGCTCTAAGCA[A/G]TCCTCCTGCCTCAGC | 51444 |
rs189155543 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | RNF138 | GRCh38.p7 | 18:32098827 | CACTGCACTCCAGCC[C/T]GGGCGACAGAGTGAG | 51444 |
rs189180969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32095112 | GAGGTGGTAATGGAG[A/G]AACAGGATTTTAATC | 51444 |
rs189300634 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32118784 | CAGTGAGTCGGGATC[A/G]TGCCACTAACACTCC | 51444 |
rs189332768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122426 | TTTTTAAACTCTGGC[A/G]TTGAGATATAGAACC | 51444 |
rs189462619 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32122865 | TAAAATTGACCACAT[C/T]GATCAAATTCTGTAG | 51444 |
rs189556983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32124506 | TTGTTTTGGCCTAGA[A/G]GTGCCATGAAAAAAT | 51444 |
rs189607485 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32100498 | TTTTTTTTTTGAGAC[A/C/G]GAGTTTTGCTCTTGT | 51444 |
rs189709139 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32099433 | TTTTAGACAAAATCT[C/T]GCTCTGTTGCCCAGA | 51444 |
rs189815275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32129060 | GTCTAATGTTTTGGG[A/C]AAAGTATTAGAGTAG | 51444 |
rs189853280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32117905 | AGCCACAGGAAGTGG[A/G]GAGGAGGAGGGAAGA | 51444 |
rs189885187 | snp | C/T | 0.0298908 | 0.118541 | upstream-variant-2KB, intron-variant | RNF138 | GRCh38.p7 | 18:32092529 | CCTCCCGCCAAGCAC[C/T]GTCCCCCATCCAGCC | 51444 |
rs189973853 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32095883 | TGAGTGTGATTGATA[C/T]AGAAGAGATTTTATG | 51444 |
rs189997444 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF138 | GRCh38.p7 | 18:32111231 | AAACCTATTAACTTT[A/G]TCCTAGAACTTCCCA | 51444 |
rs190012101 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF138 | GRCh38.p7 | 18:32102079 | GTAGAGAGGAGGTCT[C/T]GCTGTGTTACCCAGA | 51444 |
rs190104438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32123675 | TTTTTTTTTTGAGAC[A/G]GAGTCTCACTTTGTT | 51444 |
rs190106755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32127271 | CAGGTTACAAAGAGA[C/T]TAAGAGTGTAAGAGA | 51444 |
rs190190736 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130817 | ATCTTAATGAACATA[A/C]GCCTTTGTTCTGTCA | 51444 |
rs190199074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32111979 | ACTCTGAAATTCTTA[C/T]TTGAATTTTCTTGGT | 51444 |
rs190258285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32105840 | CAGATTATATCAGAA[C/T]AGATAGCTTTCTATG | 51444 |
rs190509350 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32105333 | TGACCTCAATTGATC[C/T]ACCCACCTCGGCCTC | 51444 |
rs190512783 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32110398 | TGACAAATAATGTGT[G/T]AAGCATTTTATACTT | 51444 |
rs190535185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32106265 | TTTTCCATAAGCCCT[A/G]TAAGTTTTAGTGTGC | 51444 |
rs190605181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32116923 | ATTTATTTATTTGTA[C/G]ACAGAGTTTTGCTCG | 51444 |
rs190618790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32115364 | CATCATCTCTCACTC[A/G]AACTATGATAATAGC | 51444 |
rs190735183 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNF138 | GRCh38.p7 | 18:32115793 | CACACACACACTTCC[G/T]TATTCCAAAGCCCTT | 51444 |
rs190753244 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090026 | CAAGGTGGGCGGATC[A/G]CTGGAGGCCAGGAGT | 51444 |
rs190802036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32101385 | CACCACTCCTGGCTA[A/G]TTTTTGTGTATATAT | 51444 |
rs190850000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32124680 | AAAAAATAGGAGAGC[A/G]TTATTTTTGTGTTAT | 51444 |
rs190867020 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32121354 | TACAAAATGAGCCGG[G/T]TGTGGTGGTACATGC | 51444 |
rs190922746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096670 | CAGATCATCTGCAAA[C/T]GATTGTTAAGGAAGC | 51444 |
rs191391073 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32120241 | CAGTATTACCCTGAA[C/T]TTAAGGTTTCCCCAT | 51444 |
rs191475532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122530 | GTTGCTTTTATAAAA[C/T]TGAGCACATTGGGCC | 51444 |
rs191588384 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF138 | GRCh38.p7 | 18:32096252 | AAAGTTTACCTTCAT[A/G]GCAGGGTTTTCAGCT | 51444 |
rs191591861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32097387 | TACTTCTTGTTAAGC[A/G]CAAATTTGTGTAATT | 51444 |
rs191653437 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130104 | CTTTTGTGTGTATAT[A/G]TACACATATGTGTGT | 51444 |
rs191664937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125128 | GGGAACTCATTCCTG[C/T]GCAGTAGCACAACCT | 51444 |
rs191729121 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104718 | CAATAAAAATATACA[C/T]AGCTTCTTAAAGAAA | 51444 |
rs191886132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121688 | GTTAGAAACATCTAC[C/T]AATTTTAAATGTATA | 51444 |
rs191948929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108102 | TCAGGTGATCCACCC[A/G]CCTCGGCTCCTCAAG | 51444 |
rs191951832 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32125929 | GATGTTCCAGGAAAT[C/T]TCGCTCATATTTAAG | 51444 |
rs192101629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111686 | TTATAATCACTTGTT[C/T]GTATTTAATTATAGA | 51444 |
rs192146781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098130 | TAGTTGGGATTACAG[C/G]CGTGCACCATCACGC | 51444 |
rs192158925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117868 | TGCTGCTAACATAAG[A/G]TTATATATTTTTGTT | 51444 |
rs192199697 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107287 | TGCCACGCCCAGCTA[A/G]TTTTTTTTTGTATTT | 51444 |
rs192382018 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104353 | ATTAAGGGTGGCTTC[C/T]CTAAAATCTATAGCA | 51444 |
rs192425349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098578 | AAGGTTGAGGCCGGG[C/T]GCAGTGGCTCACGCC | 51444 |
rs192455084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32126589 | AAAATGCTTCTCACG[C/T]AGATATTTTTGGTAA | 51444 |
rs192465487 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091921 | CACACCCCGTGCCTC[C/T]CCGCCTCTCCTGGCT | 51444 |
rs192525134 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF138 | GRCh38.p7 | 18:32099034 | TGGGAGCATGATGAG[C/T]GGGAATATTGTTTTT | 51444 |
rs192641900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32093580 | TTCCCCTTTGTTTTA[C/T]CTTTCTGCTTACTTA | 51444 |
rs192685216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103471 | GTGTTGAGATTATAG[A/G]TGCGAGCCACTGTGT | 51444 |
rs192752218 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112797 | TCTGGATTTTATTCT[A/T]TCATTTGGAGAAGGA | 51444 |
rs192795286 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32118248 | TGGATAGTAATCCTT[C/T]GTTATGGCTGGGCGC | 51444 |
rs192877980 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF138 | GRCh38.p7 | 18:32122234 | GAGAGATAACATTGT[C/T]ATCTTCACAGAAGTG | 51444 |
rs192939920 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32109455 | ATTATTACTATTTTT[A/T]TAGAGACAGGGTCAT | 51444 |
rs193151071 | snp | C/G | 3.05759e-05 | 0.00390986 | intron-variant | RNF138 | GRCh38.p7 | 18:32113697 | TACACTATTTCAAAT[C/G]TTACGAGTTCTATTT | 51444 |
rs193238873 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116986 | AGCTCACTACAACAT[C/T]GACCTCCCAGGTTCA | 51444 |
rs193302355 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF138 | GRCh38.p7 | 18:32094662 | GATCTTCCACCTTTA[A/G]TCTAGCATAACTTGG | 51444 |
rs199597143 | in-del | -/TGTGT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097973 | GTGTGTGTGTGTGTG[-/TGTGT]TATTTTTGTTTGTTT | 51444 |
rs199606001 | in-del | -/TATAT | 0.0174175 | 0.0916809 | intron-variant | RNF138 | GRCh38.p7 | 18:32111506 | AATATTTATTCATCA[-/TATAT]TATGTTAAGAAGTTG | 51444 |
rs199689495 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116736 | TTTTGATTTTTTGGG[G/T]TGGGGGGGTGGTTTT | 51444 |
rs199700256 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32117451 | CTGAAGAAGAGAGCT[C/G]AATAGAGCATGGCTA | 51444 |
rs199720611 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097976 | TGTGTGTGTGTGTGT[G/T]TTATTTTTGTTTGTT | 51444 |
rs199752645 | snp | A/G | 0.000428463 | 0.0146304 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129197 | ATCTGAAGGCTGTAG[A/G]CATCTCTGCATCTTT | 51444 |
rs199775904 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098567 | ATTATATAATAAAGG[G/T]TGAGGCCGGGCGCAG | 51444 |
rs199877493 | in-del | -/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101231 | TTTTTTTTTTTTTTT[-/C]AAAGACAGAGTCTGG | 51444 |
rs199886842 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130916 | AAAACAGCTCCTTTT[A/T]AAGACTTTTGACCAT | 51444 |
rs199947485 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121206 | AAAATAAAAATTTTT[C/T]CAATCCTGGCCAGGT | 51444 |
rs200018900 | snp | A/G | 0.00140548 | 0.026472 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111875 | TTAGACCTTGAAAAT[A/G]TAATGAGGAAGTTTT | 51444 |
rs200179767 | in-del | -/T | 0.426813 | 0.17674 | intron-variant | RNF138 | GRCh38.p7 | 18:32109157 | TTTTTTTTTTTTTTT[-/T]AAACAAGGTCTCACT | 51444 |
rs200182726 | in-del | -/ATG | | | utr-variant-3-prime, cds-indel, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129489 | GAATTTTTCATTATT[-/ATG]TTGCTTTTGAAATTT | 51444 |
rs200268899 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098559 | GCTATTTAATTATAT[A/T]ATAAAGGTTGAGGCC | 51444 |
rs200339274 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102798 | ACACCACGCCCAGCT[A/G]ATTTTTATTTTCAGT | 51444 |
rs200397562 | in-del | -/A | 0.0271762 | 0.113356 | intron-variant | RNF138 | GRCh38.p7 | 18:32117505 | CATGCAACTGAGTAG[-/A]AAAAAAAAATTGCAA | 51444 |
rs200419702 | snp | C/T | | | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091278 | CGGCCTTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 51444 |
rs200452567 | snp | C/T | 0.00131225 | 0.0255813 | intron-variant | RNF138 | GRCh38.p7 | 18:32111736 | TTTGTAATTAATGTG[C/T]CACAATGTTTGGTTT | 51444 |
rs200490346 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116737 | TTTGATTTTTTGGGG[G/T]GGGGGGGTGGTTTTT | 51444 |
rs200519159 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32105289 | TAGAGACAGGTTTCA[C/G]CATGTTGGCCAGGCT | 51444 |
rs200542926 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128962 | TTCAAATCTTGTATC[G/T]TAAAAGATACTGTTA | 51444 |
rs200603930 | in-del | -/T | 0.0115144 | 0.0749975 | intron-variant | RNF138 | GRCh38.p7 | 18:32114604 | ATTCCTTTGATTTTC[-/T]TTTATGTATCATCAC | 51444 |
rs200622689 | in-del | -/A | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121133 | GAGTGAGACTGTCTC[-/A]AAAAAAAAACAAAAC | 51444 |
rs200657573 | snp | A/C | 1.67097e-05 | 0.00289043 | intron-variant | RNF138 | GRCh38.p7 | 18:32126808 | AATTTGTGGTAAGTG[A/C]ATTCTTCAAGATTAA | 51444 |
rs200664026 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117644 | TTTTTCCATGTATCT[A/T]ACTGTAAGCTATAAC | 51444 |
rs200719006 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107122 | CCTTTTTTCCTTTTT[C/T]TTTTTTTTTTTTTTT | 51444 |
rs200779716 | in-del | -/A | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096898 | GGCTATTAAAAAAAA[-/A]TTTTTTTGTAGAGAT | 51444 |
rs200800390 | snp | A/G | 0.00199802 | 0.0315439 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113817 | TATGGTGTTTCTTCT[A/G]TCATTCCAAACTTTC | 51444 |
rs200854903 | in-del | -/TA | 0.0283406 | 0.115616 | intron-variant | RNF138 | GRCh38.p7 | 18:32101393 | TGGCTAATTTTTGTG[-/TA]TATATATATATATTT | 51444 |
rs200968240 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106548 | TTATTTTTTATTTTA[-/T]TTTATTTATTTATTT | 51444 |
rs201012505 | snp | C/T | 3.66952e-05 | 0.00428325 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092809 | TGCGGCCACGTCCTA[C/T]ACCGAAGATGATTTC | 51444 |
rs201079363 | in-del | -/T/TTA | 0.446902 | 0.154045 | intron-variant | RNF138 | GRCh38.p7 | 18:32095178 | TTTTAAAAATTATCG[-/T/TTA]TTTTTTTTTGAGACA | 51444 |
rs201245094 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101214 | ACCTCTTATAGGTTT[C/T]TTTTTTTTTTTTTTT | 51444 |
rs201330717 | snp | G/T | | | utr-variant-3-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32131020 | ACCATTCTGGGATTT[G/T]CAAAGTTTAATACAT | 51444 |
rs201369742 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130917 | AAACAGCTCCTTTTT[A/G]AGACTTTTGACCATA | 51444 |
rs201417806 | in-del | -/T/TA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094796 | ATATATATATATATA[-/T/TA]AAGCAGGTCTTTTTT | 51444 |
rs201468470 | snp | C/T | 7.64146e-05 | 0.00618073 | intron-variant | RNF138 | GRCh38.p7 | 18:32126651 | TGTATAATATTTCAT[C/T]GTTTTTATTATTTTT | 51444 |
rs201483037 | in-del | -/TGA | 0.0138799 | 0.0821421 | intron-variant | RNF138 | GRCh38.p7 | 18:32119917 | TGTTTTCAGCAGCTT[-/TGA]TGATTTGTTAGTTGT | 51444 |
rs201707524 | in-del | -/A | 0.0248432 | 0.108648 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091592 | ATCGGTCATGCTGTT[-/A]AAAGGAGAAAGTGGA | 51444 |
rs201727728 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131380 | TATGGGGAAAAGTTT[A/T]TTTTTAATATTACTT | 51444 |
rs201799229 | in-del | -/AA | 0.0295035 | 0.117819 | intron-variant | RNF138 | GRCh38.p7 | 18:32112664 | TCCAAACTGGGCAAC[-/AA]GAGCGAAACGCTGTC | 51444 |
rs201818453 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130915 | AAAAACAGCTCCTTT[A/T]TAAGACTTTTGACCA | 51444 |
rs201905724 | in-del | -/TGTG | 0.0138799 | 0.0821421 | intron-variant | RNF138 | GRCh38.p7 | 18:32128643 | TGACACATTTATGAT[-/TGTG]TGTTATGATTAACTT | 51444 |
rs201955751 | snp | C/T | 0.000243962 | 0.0110418 | intron-variant | RNF138 | GRCh38.p7 | 18:32113701 | CTATTTCAAATCTTA[C/T]GAGTTCTATTTTAAA | 51444 |
rs201961262 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | RNF138 | GRCh38.p7 | 18:32115131 | TTCTTAAGTGAGGGG[-/A]TGGTGTTTGTCTTGT | 51444 |
rs201966280 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107467 | TTTAAATTTTAGCAG[-/T]TTTTTTTTTAAAGGC | 51444 |
rs202002141 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101569 | ATTAAGAAAAATTTA[-/T]TTTTTTTTTAAGAAT | 51444 |
rs202005922 | in-del | -/TA | 0.446641 | 0.154377 | intron-variant | RNF138 | GRCh38.p7 | 18:32097939 | GTGTATATGTGTATG[-/TA]TATATGTGTGTGTGT | 51444 |
rs202027202 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107123 | CTTTTTTCCTTTTTT[C/T]TTTTTTTTTTTTTTG | 51444 |
rs202040476 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF138 | GRCh38.p7 | 18:32099068 | CTCCCAGTGTTGTTG[A/G]TTAGCCTTTTGTTGG | 51444 |
rs202193372 | in-del | -/ACTTA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122473 | TTTTTCTTAGCCACT[-/ACTTA]TCTTATTACTGTGTT | 51444 |
rs202220582 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113368 | CAGCCAGGAACTTAA[A/T]TTTTTTTTAAGTGCT | 51444 |
rs367715581 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32119296 | ATTGAGGCAGGGTCT[C/T]GCTATGTTTCCCAGG | 51444 |
rs367863587 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121342 | CTTTACTAAAAATAC[A/G]AAATGAGCCGGGTGT | 51444 |
rs367925343 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102659 | TTTTTTTGAGAAATA[A/G]TCTCCTTCCGTTGCC | 51444 |
rs368006147 | in-del | -/T | 0.499879 | 0.0077866 | intron-variant | RNF138 | GRCh38.p7 | 18:32097977 | GTGTGTGTGTGTGTG[-/T]TATTTTTGTTTGTTT | 51444 |
rs368146261 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF138 | GRCh38.p7 | 18:32098745 | GTAATCCCAGCTGTT[C/T]GGGAGGCTGAGGCAG | 51444 |
rs368148110 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32103299 | AGTTAAGGAATTCTA[C/T]TGCCTCATCCTTGCA | 51444 |
rs368229430 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101895 | CATTTTTGCTTGTTT[A/G]AGACAGGGTCTAACT | 51444 |
rs368237775 | snp | C/G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093471 | GAGAGCGTTTTGTTT[C/G/T]GTTTCCAGTCCACTA | 51444 |
rs368247267 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129242 | CATCTTTAAGGGGGA[A/G]ACTACATGAAGTCAC | 51444 |
rs368315264 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | RNF138 | GRCh38.p7 | 18:32116290 | AGCTACTCAGTAAAA[G/T]CCTTCCTGAGCTCTA | 51444 |
rs368472041 | snp | G/T | 6.64341e-05 | 0.00576304 | intron-variant | RNF138 | GRCh38.p7 | 18:32123511 | TTTTTCCCCTGTGCT[G/T]CTTAAGCAATAGGAG | 51444 |
rs368518701 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32109953 | ATCTTGTTTACTTTG[C/T]GTTATTTTGGTTTCT | 51444 |
rs368522883 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113073 | GTTCCAAGTATTCCT[A/G]GCAACTTAATTTTTT | 51444 |
rs368598319 | in-del | -/AAT | 0.0158469 | 0.0875917 | intron-variant | RNF138 | GRCh38.p7 | 18:32103463 | TCCCAAAGTGTTGAG[-/AAT]ATTATAGGTGCGAGC | 51444 |
rs368773507 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102938 | GCCTGGCCAATTTGG[A/G]ATTTTCTAACAAAAT | 51444 |
rs368775295 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108145 | CAGGCGTAAGCCACC[A/G]TGCCTGGCCAAATAT | 51444 |
rs368828041 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111999 | TTTTCTTGGTTGGTG[-/T]TTTTTTTTTTTTTTG | 51444 |
rs368833655 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093167 | GGCTTTCGCGCCCCC[A/G]GGGCAGTGGCCAGGC | 51444 |
rs368889195 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090474 | CAAAAATACAAAATA[C/T]AGTTTGGTAGAGGGA | 51444 |
rs368944212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32115473 | ATTCTGGCTGGGCGC[A/G]GTGGCTCACACCTGT | 51444 |
rs368971809 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100468 | ACCACACCCAACTAA[C/T]TTTTTTTTTTTTTTT | 51444 |
rs368990406 | snp | C/T | 0.000436359 | 0.0147644 | intron-variant | RNF138 | GRCh38.p7 | 18:32124857 | TGTGGTAAGTACATA[C/T]GTTTGAGACAGTCTT | 51444 |
rs369057752 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094050 | CCCGCCTCGGCCTCC[C/T]AAAGTGCTGGGATTA | 51444 |
rs369279489 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099650 | CCCCAAATGATCTGC[C/T]CCGCCTCGGCCTCCC | 51444 |
rs369363220 | snp | C/G/T | 0.000194628 | 0.00986287 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092851 | CTGTCAGGAGGTGCT[C/G/T]AAAACGCCCGTGCGG | 51444 |
rs369510280 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128294 | TGTCATCCCAGTACT[G/T]TGGGAGGCCGAGGCG | 51444 |
rs369545636 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095696 | ACTACTGACTATCCT[A/G]GTAAAAGGAGCAAGT | 51444 |
rs369559489 | in-del | -/A | 0.0228947 | 0.104514 | intron-variant | RNF138 | GRCh38.p7 | 18:32098688 | AACCCTGTCTCTACT[-/A]AAAAATACAAAAAAA | 51444 |
rs369595892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32110981 | GAGACGAGATTTCAC[C/T]GTGGTAGCCAGAATG | 51444 |
rs369606904 | snp | C/T | 3.30338e-05 | 0.00406397 | missense, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32126709 | CATGTCCTATTTGTG[C/T]GTCTCTTCCTTGGGG | 51444 |
rs369691207 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099701 | GTGAGCCACTGCACC[C/T]GGCCATTCTTTGTAC | 51444 |
rs369818590 | snp | G/T | 1.65798e-05 | 0.00287917 | intron-variant | RNF138 | GRCh38.p7 | 18:32129075 | CAAAGTATTAGAGTA[G/T]TTGAATATGTTTTTC | 51444 |
rs369851930 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104140 | TGACTTAGCCTCCCA[A/G]ATAGTTGGGATTACA | 51444 |
rs370174742 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117852 | TTTTATAACAACATT[C/T]TGCTGCTAACATAAG | 51444 |
rs370223896 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127291 | AGTGTAAGAGAAGTT[A/G]TATAATGTAAAAATG | 51444 |
rs370275912 | in-del | -/AATAAT | 0.0120068 | 0.0765455 | intron-variant | RNF138 | GRCh38.p7 | 18:32118842 | CTCAAAAAAAAAGAA[-/AATAAT]AATAATAATAATAAT | 51444 |
rs370415792 | in-del | -/TA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094781 | GTAATAGCTGCTAAC[-/TA]TATATATATATATAA | 51444 |
rs370418769 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121040 | CTCGGGAGGCTGAGG[C/T]ACGAGAATCACTTGA | 51444 |
rs370521742 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091904 | CTATACAGGCCGCAC[C/T]TCACACCCCGTGCCT | 51444 |
rs370605226 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | RNF138 | GRCh38.p7 | 18:32126842 | AGTACTGTTTAAATA[C/T]TAAAGTTAAAATAAC | 51444 |
rs370639399 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093273 | GGAGCCTTTTTGTTT[C/T]TTAGCAACCCGGGTG | 51444 |
rs370706503 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF138 | GRCh38.p7 | 18:32102337 | CTCCCGAGTAGCTGG[A/G]ACTACAGGCGCCCGC | 51444 |
rs370933289 | in-del | -/TA | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32103028 | TTTGTCTTTATAGCC[-/TA]TATATATATACATGT | 51444 |
rs371005849 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32122394 | AAGGAAAAATGAATA[A/C]CCAGTTTAAGTTCAA | 51444 |
rs371223053 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107298 | GCTAATTTTTTTTTG[G/T]ATTTTAGTAGAGACG | 51444 |
rs371255126 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101577 | AAAATTTATTTTTTT[G/T]TAAGAATTCAAGATC | 51444 |
rs371299342 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32103534 | TGTGTACCTGATATT[C/G]AAGGCACCAAGAAAA | 51444 |
rs371512456 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102708 | CACTATCTCGGCTCA[C/G]TGAAACCTCCATCTC | 51444 |
rs371602944 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121885 | TATGTACTTTTTTTT[-/T]CAGACTGAGTTTCGC | 51444 |
rs371635992 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102347 | GCTGGGACTACAGGC[A/G]CCCGCCGCCACGCCC | 51444 |
rs371665134 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094078 | TTAAAGGCGTGAGCC[A/C]CCGCGCCCCGCCCGG | 51444 |
rs371730178 | snp | C/T | 3.50067e-05 | 0.00418355 | intron-variant | RNF138 | GRCh38.p7 | 18:32124890 | GCTTAGAATAAAACA[C/T]GCTGTTCTATTTATT | 51444 |
rs371780031 | snp | C/G | 1.66001e-05 | 0.00288094 | intron-variant | RNF138 | GRCh38.p7 | 18:32123512 | TTTTCCCCTGTGCTT[C/G]TTAAGCAATAGGAGT | 51444 |
rs371897894 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104268 | TCCCCCCACTTCGGC[A/G]TCCCAAAGGGCTGAG | 51444 |
rs371901863 | snp | A/C | 1.65718e-05 | 0.00287848 | intron-variant | RNF138 | GRCh38.p7 | 18:32129080 | TATTAGAGTAGTTGA[A/C]TATGTTTTTCCTGTT | 51444 |
rs371975908 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111075 | GTGAGCCACCGTGCC[C/T]GGCAAAGCCGGAAGT | 51444 |
rs371987528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32123186 | AACCTTACTAGTCTA[A/G]GTAAAGGTAGAGGAA | 51444 |
rs372011672 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125187 | GTAGATGGCAGACAA[A/G]TAGATCTAGTCAGGT | 51444 |
rs372034185 | in-del | -/TT | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130875 | TGCTTGAGCATTTTC[-/TT]TTTCAGTTACATGGG | 51444 |
rs372115827 | in-del | -/TTTA | 0.0558977 | 0.157557 | intron-variant | RNF138 | GRCh38.p7 | 18:32106549 | TATTTTTTATTTTAT[-/TTTA]TTTATTTATTTATTT | 51444 |
rs372179990 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32103944 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 51444 |
rs372282880 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115784 | GCACGCACGCACACA[C/T]ACACTTCCTTATTCC | 51444 |
rs372304038 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116554 | TAAATTTATTTTGTT[C/T]GTTCTGTTTTGTTTT | 51444 |
rs372489868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101425 | TAAATTAGAGTCAGG[G/T]TTTCACCATGTTGGC | 51444 |
rs372611685 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32099944 | CAAATATTTCTGATA[C/T]ATCACACAAGAATAA | 51444 |
rs372699780 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096044 | TGAATGTGAGCTGGA[C/T]TTTGAAGTTTGGCTG | 51444 |
rs372760387 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093374 | CTGCTTTCAAGTTTC[C/G]TCTTTCAGAACCTTG | 51444 |
rs372818872 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126105 | ACTTCATTTAAACGT[A/C]AGGATATGGCTGGGT | 51444 |
rs372942832 | in-del | -/A | 0.498652 | 0.0259235 | intron-variant | RNF138 | GRCh38.p7 | 18:32123965 | CCATAAATTAAACTT[-/A]AAAAAAAAAAAAAAA | 51444 |
rs372991214 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF138 | GRCh38.p7 | 18:32119892 | AGTAAGTTGATTTTT[A/G]TGTTAATCTTGTTTT | 51444 |
rs373006418 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32095706 | ATCCTAGTAAAAGGA[A/G]CAAGTTCATTATCAT | 51444 |
rs373024422 | snp | C/T | | | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131606 | GGCAAACATTTAACT[C/T]TCATAATTCACACTG | 51444 |
rs373074195 | snp | C/G/T | 0.000100168 | 0.00707636 | intron-variant | RNF138 | GRCh38.p7 | 18:32126807 | GAATTTGTGGTAAGT[C/G/T]AATTCTTCAAGATTA | 51444 |
rs373082606 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090478 | AATACAAAATATAGT[C/T]TGGTAGAGGGAATTA | 51444 |
rs373200041 | snp | C/T | 3.30666e-05 | 0.00406598 | intron-variant | RNF138 | GRCh38.p7 | 18:32129092 | TGAATATGTTTTTCC[C/T]GTTGACATGAATGTT | 51444 |
rs373202145 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32121585 | TGATATTATAGTTCT[A/G]TAAACCTATTAGAAG | 51444 |
rs373250124 | snp | A/C/T | 0.000995166 | 0.0222844 | intron-variant | RNF138 | GRCh38.p7 | 18:32092900 | GTGTGAGTAGACGCC[A/C/T]CCTCCCCCTCGCGGA | 51444 |
rs373265969 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099713 | ACCCGGCCATTCTTT[A/G]TACCTGTTATCACAG | 51444 |
rs373448151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32126388 | ATATGTTGCAGGCAG[C/T]CAGTTAGTGATAACT | 51444 |
rs373677086 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130921 | AGCTCCTTTTTAAGA[C/G]TTTTGACCATAGTGT | 51444 |
rs373812439 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108559 | TACCATAATTAGTTA[C/T]GCATTCTTCTGTTGG | 51444 |
rs373951915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32104264 | ATGATCCCCCCACTT[C/T]GGCGTCCCAAAGGGC | 51444 |
rs374052423 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114236 | TGTTTTTTCTTTGCT[A/G]TCTAAGGGATAGACT | 51444 |
rs374060269 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091963 | ATCCCCGGCGCTCCC[C/G]CGTTCGGTGACGGCC | 51444 |
rs374063728 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113400 | TCTAACTCTGCCAGG[A/C]TGCAGAAGTTAAATA | 51444 |
rs374063860 | in-del | -/GTCAAGATGTGTAATGTGT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32129018 | GTGTGTGTAATGTGT[-/GTCAAGATGTGTAATGTGT]ATCAAGATGTCTAAT | 51444 |
rs374136278 | in-del | -/ATCA | 0.0158469 | 0.0875917 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130222 | TTTAAAATTTTGTAT[-/ATCA]ATCACCAAATTTTTA | 51444 |
rs374139406 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107566 | CACCCTGTCACCCAG[G/T]CTGGAGTGCAATGGC | 51444 |
rs374409777 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107116 | CACTTTCCTTTTTTC[C/T]TTTTTTTTTTTTTTT | 51444 |
rs374513795 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093855 | GATGATCAGAGTCCC[C/T]GGGGAACTTTTTAAG | 51444 |
rs374578997 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32109525 | GAGACCCTCCCACCT[C/G]AGCCTCCCAAGTGGC | 51444 |
rs374673906 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32122017 | GGGATTACAGGCGCC[C/T]GTCACCACACCCGGC | 51444 |
rs374772322 | in-del | -/TT | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131378 | TTATGGGGAAAAGTT[-/TT]TWTTTTTAATATTAC | 51444 |
rs374800444 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF138 | GRCh38.p7 | 18:32109872 | GCCTGGGCGACAGAG[C/T]GAGGCTCTGTCTCAA | 51444 |
rs374855875 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112261 | AAATTCACCCCTTAA[A/G]TTTTTCTCATGGTAG | 51444 |
rs374904320 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125708 | AGGCCGAGAGGGGAG[C/G]ATTGCTTGAGCCCAG | 51444 |
rs374909998 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102937 | TGCCTGGCCAATTTG[A/G]GATTTTCTAACAAAA | 51444 |
rs374932978 | snp | A/C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117317 | TTTAGTAAAGAGACT[A/C/G]TTTTCAAAGAGTAGT | 51444 |
rs375005834 | snp | A/G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123739 | CTCACTGCAACCTGC[A/G/T]CCTCTCAGGTTCAAG | 51444 |
rs375038122 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32124445 | ACAATTAAGTTTGGA[C/T]CTAACTACATAATAT | 51444 |
rs375156722 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126002 | TTCTGCATAATATTC[A/G]ATATATCATAAACTT | 51444 |
rs375278006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32116108 | TTAATAAATAAGTTA[A/G]TACAGGTAAAGAAAC | 51444 |
rs375289132 | in-del | -/CA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127214 | CTAGCATGTAAGACA[-/CA]ACGTTTTTAAAAATG | 51444 |
rs375453268 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF138 | GRCh38.p7 | 18:32104284 | TCCCAAAGGGCTGAG[A/C]TTACATGCATAAGCC | 51444 |
rs375703068 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | RNF138 | GRCh38.p7 | 18:32121137 | TGAGACTGTCTCAAA[A/G]AAAAACAAAACAAAA | 51444 |
rs375721132 | snp | C/G | 0.000210841 | 0.0102653 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092800 | GGACCTCTCTGCGGC[C/G]ACGTCCTACACCGAA | 51444 |
rs375810742 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123653 | CTTTTTAAATTAAAC[-/T]TTTTTTTTTTTTTTT | 51444 |
rs375835981 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097979 | GTGTGTGTGTGTGTT[A/G]TTTTTGTTTGTTTGT | 51444 |
rs375862187 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125585 | ATGTTATCAATAAGA[A/G]CTGTAGATATTTCTA | 51444 |
rs375974010 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | RNF138 | GRCh38.p7 | 18:32103824 | AAAAAAAATTAGCCG[C/G]GCGCGGTGGCGGGCA | 51444 |
rs376076560 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115492 | GCTCACACCTGTAAT[A/C]CCAGCATTTTGGGAG | 51444 |
rs376197235 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32120729 | TAGATAGAAGGGAGA[A/G]CGTGTTTAAAAAGGG | 51444 |
rs376215746 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF138 | GRCh38.p7 | 18:32098760 | CGGGAGGCTGAGGCA[A/G]GAGAATGGCATGAAC | 51444 |
rs376517746 | snp | A/C | 4.97649e-05 | 0.00498798 | intron-variant | RNF138 | GRCh38.p7 | 18:32129069 | TTTGGGCAAAGTATT[A/C]GAGTAGTTGAATATG | 51444 |
rs376542095 | in-del | -/GTGCAG | 0.00795532 | 0.062565 | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32091019 | GTCGCCAGGGCTGGA[-/GTGCAG]CGGCGCGATCGCGGC | 51444 |
rs376759761 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111225 | TGGGTAAAACCTATT[A/G]ACTTTATCCTAGAAC | 51444 |
rs376913015 | snp | A/T | 0.000153988 | 0.00877327 | intron-variant | RNF138 | GRCh38.p7 | 18:32126657 | ATATTTCATTGTTTT[A/T]ATTATTTTTTGTTTA | 51444 |
rs376986492 | snp | A/C | | | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090620 | TCCATTTCCTATCCT[A/C]ATTATAGCCATCGTT | 51444 |
rs377116014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32126165 | TTTGGGAGGCCAAGG[C/T]GGGAGGATTGCTTGA | 51444 |
rs377249875 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32107621 | TGCCTCCCAGGTTCA[A/G]GTGATTCTCCTACCT | 51444 |
rs377285957 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128079 | TGCGAGACTCCGTCT[A/C]AAAAAAGAAAAGTAG | 51444 |
rs377353387 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101691 | GTCATGTTGCTTTCC[C/T]AAAAATTGAGCTAAT | 51444 |
rs377526920 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130313 | GTTTACACACACACA[A/G]TTACCTGTTTATATG | 51444 |
rs377672524 | snp | A/G | 1.68108e-05 | 0.00289916 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111787 | CCTGACTGCAATGAG[A/G]GAAAGCGGAGCACAT | 51444 |
rs377731440 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF138 | GRCh38.p7 | 18:32101521 | TTTTATTTTTTTAAG[C/T]CTTAGTTTCCTCATC | 51444 |
rs377761680 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128308 | TGTGGGAGGCCGAGG[C/T]GGGTGGATCACCTGA | 51444 |
rs386802177 | multinucleotide-polymorphism | AT/GC | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118563 | ATGCCGGGCGCAGTG[AT/GC]TCACGCCTGTAATCC | 51444 |
rs397747802 | in-del | -/AAAAG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128091 | CTCAAAAAAGAAAAG[-/AAAAG]TAGGTGATCTAATTA | 51444 |
rs397806882 | in-del | -/T | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32098564 | CGCCCGGCCTCAACC[-/T]TTTATTATATAATTA | 51444 |
rs397967617 | in-del | -/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114878 | AGTTGAAATTTCTGG[-/G]TAAAAACCTTTAGTG | 51444 |
rs397976466 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107137 | TTTTTTTTTTTTTTT[-/T]GGAGACGGAATCTCG | 51444 |
rs398120285 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115022 | TTATAGTTTTTTTTT[-/T]AGTCCTTCTGGGTTT | 51444 |
rs527273949 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091947 | TGGCTCCTCCGCCCA[A/G]ATCCCCGGCGCTCCC | 51444 |
rs527337814 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF138 | GRCh38.p7 | 18:32092555 | CAGCCCCCTGTGGGA[A/G]GAGCCGTGGGAGGGG | 51444 |
rs527468724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32118645 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCTTGTC | 51444 |
rs527556565 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32100862 | TGCTCGCCTTGGCCT[C/G]CCAGAGTGCTGGGAT | 51444 |
rs527593881 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32115184 | TAAAGTTCTTAGTAT[A/T]CATGATTGTAATCAC | 51444 |
rs527681429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32106230 | GACAAGGTTGCACGA[A/G]TGGTCTATTCCAACC | 51444 |
rs527712160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32100223 | ATATATATATATATA[A/T]AATCTTTGGTTGTAC | 51444 |
rs527989615 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32109265 | CTCAAGTGATCCTCT[A/C]ACCTCAGCCTCCTGA | 51444 |
rs527996071 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32093490 | TCCAGTCCACTATGT[G/T]TTAGAGGGATCTAGA | 51444 |
rs528104142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102579 | ATATTTGAAGAGTTT[A/G]TATTGTACAGTTTGT | 51444 |
rs528141573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32114813 | TTTAGTAACTTAACC[A/G]CCCTTAAGCACTTCA | 51444 |
rs528151826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122130 | CCTCAGCCTTGCAAA[A/G]TGCTGGGATTACAGG | 51444 |
rs528194796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32115724 | CACTCTAGCCTGGGC[A/G]ACAGAGTCAGACTCC | 51444 |
rs528293665 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129800 | AGCTTGTTGTAAAGA[C/T]ATTTTCTTTTTGTTA | 51444 |
rs528298363 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090434 | TCTTGCTTCCACTGC[A/G]CTTGCTGCTAAGGAG | 51444 |
rs528424799 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32094032 | TCCTGACCTCGTGAT[-/C]CTCCCGCCTCGGCCT | 51444 |
rs528446026 | snp | C/T | 0.000116913 | 0.0076448 | intron-variant | RNF138 | GRCh38.p7 | 18:32123502 | GGTATTAACTTTTTC[C/T]CCTGTGCTTCTTAAG | 51444 |
rs528459510 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | RNF138 | GRCh38.p7 | 18:32116531 | TTTTTTTTTTTTTTT[A/T]AAATTTTTAAATTTA | 51444 |
rs528589063 | in-del | -/TATT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100305 | ATTATTTTATATATA[-/TATT]TGAGACAGGGTCTTT | 51444 |
rs528602430 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131983 | TCATAACTTCTACAG[A/G]AACCCCTTAACAGCT | 51444 |
rs528689733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32104089 | CCTGATCTTGGCTCA[C/G]TGCAACCTCTGCCTT | 51444 |
rs528703156 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32120692 | GATGACAGTAATAGT[A/G]GAAAATTGAGAGTTA | 51444 |
rs528726764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32104653 | AAAAATTAATAGAAG[A/G]AAAACGTCACTTACA | 51444 |
rs528787202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32110275 | TGGGATTATAGGCAT[A/G]AGCCACTACGCCCTG | 51444 |
rs528938342 | in-del | -/TTAC | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32125948 | CTCATATTTAAGATT[-/TTAC]TTAGTTTTATATTGG | 51444 |
rs528992303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32126103 | GTACTTCATTTAAAC[C/G]TAAGGATATGGCTGG | 51444 |
rs528995389 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113590 | TGTATTATCTATTCT[C/T]AACTCCTACTTAAGG | 51444 |
rs529091522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32107044 | CTCTTTCTGTCTCCT[A/G]TGGCTACTGGGCCAC | 51444 |
rs529129891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32100921 | GAGATATATTTAAAT[C/T]AAAATAAATGCTCAG | 51444 |
rs529170110 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32112155 | AATACTTAGCGTGGC[A/T]TTTTTCTAAAAGTAA | 51444 |
rs529179027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32112662 | ACTCCAAACTGGGCA[A/G]CAAGAGCGAAACGCT | 51444 |
rs529337877 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32120480 | TGGGAAAATAATTTT[C/T]TGTTTTTGTTTTATT | 51444 |
rs529371126 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115606 | AAAAATTAGCTGGAC[A/G]TGGTGGCGCGTGCCT | 51444 |
rs529632935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32121063 | TCACTTGAACCCAGG[A/G]GGAGGAGTTTGCAAT | 51444 |
rs529643054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32097853 | GAAACAGGGTCTCAC[A/T]CTGTTGCTCGGGCTA | 51444 |
rs529653103 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091549 | CCCAAAGGTGTAGTA[C/G]AAGACTGCATCTGCG | 51444 |
rs530026227 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116632 | ACATGGCTCACTGTA[A/G]CCTTGACCTCCTGGG | 51444 |
rs530026351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111338 | ACAAAAGCTTATGTT[A/G]CTCATCCTTTTATTT | 51444 |
rs530142056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32118557 | ATAATAATGCCGGGC[A/G]CAGTGGCTCACGCCT | 51444 |
rs530259680 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32103419 | GCTGGTCTTGAACTC[C/T]TAGGCTCAAATAATC | 51444 |
rs530265026 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32108824 | CAGGCATGCACCACC[A/G]TGCCCAGCTAATTTT | 51444 |
rs530268946 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32093275 | AGCCTTTTTGTTTCT[G/T]AGCAACCCGGGTGAA | 51444 |
rs530409832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32114768 | CTAATATTTTATTTT[A/G]GTAGCCTTTCATTTT | 51444 |
rs530414005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32107778 | CGCCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 51444 |
rs530438263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32099512 | GGTTCAAGAGATTCT[C/T]CTGCCCCAATCTCCC | 51444 |
rs530488688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121028 | TAGACCCAGCTACTC[A/G]GGAGGCTGAGGCACG | 51444 |
rs530526252 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094054 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTAAAGG | 51444 |
rs530598719 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119725 | CACTGCCCCCAGCCT[C/G]TTTCTCATTTAAAAA | 51444 |
rs530629458 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111276 | CTCTTTTGTAGTAGA[C/T]CTGTTTATGTCTTGT | 51444 |
rs530688430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108357 | CCTCCTTCAGGATAC[A/C]ATTATCCTGACCTTT | 51444 |
rs530731855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32102481 | ACTGGGATTACAGGC[A/G]TGAGCCACTGTGCCT | 51444 |
rs530912312 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130554 | ATGCTTTCTTTAAAA[C/T]AACTAGAAGAACATA | 51444 |
rs530950926 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129639 | ATAGAAACTTGAAGT[A/G]CTAAATGGAATAATC | 51444 |
rs530960673 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099709 | CTGCACCCGGCCATT[C/T]TTTGTACCTGTTATC | 51444 |
rs531036167 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126024 | CATAAACTTTGGCTA[G/T]AGTTTAATTACTGAA | 51444 |
rs531036986 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32103360 | TACCTCACTAATTTT[A/T]AAAAATTTTTGTAGA | 51444 |
rs531118804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109531 | CTCCCACCTCAGCCT[C/T]CCAAGTGGCTAAGAC | 51444 |
rs531202346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122678 | AAAATACAAAAATTA[A/G]CCGGTCATGGTGGCT | 51444 |
rs531232974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32116342 | ACTGTTCTTTATGCT[A/G]TTAGATCTCTAAACT | 51444 |
rs531310864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32110344 | TCTAGTGCTGCTTTA[A/G]TGATATTAACTACTA | 51444 |
rs531357785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125304 | GCATAAAGCAAGGAA[A/G]GAAAAGACTTAGACT | 51444 |
rs531385319 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092229 | AACGCCGCTTCGGGG[A/C]TCCTAGGTGAGAGTC | 51444 |
rs531455941 | snp | C/G/T | 0.000981836 | 0.0221349 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092619 | CTCTGCGTTCGGCCC[C/G/T]GCCCTACCCAGGGCC | 51444 |
rs531595384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32118690 | AAAAATTAGCTGGGC[G/T]TGGTGGTGCGCGCCT | 51444 |
rs531606473 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32100871 | TGGCCTCCCAGAGTG[C/T]TGGGATCACAGGCCT | 51444 |
rs531620961 | in-del | -/ACTT | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131460 | AAATTTCACAATACC[-/ACTT]ACTTAGGAAAGCTAT | 51444 |
rs531684062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32119300 | AGGCAGGGTCTCGCT[A/G]TGTTTCCCAGGCCCG | 51444 |
rs531814414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112598 | GCTGAGGCAGAATTG[G/T]TTGAACCTGGGCGGC | 51444 |
rs531844365 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32100333 | GTCTTTCTCTGTTGC[C/T]CTGTTGCCCAGGCTA | 51444 |
rs532079655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108988 | TATATAGGTTTGATG[A/G]GTATATACTTCAGAG | 51444 |
rs532115205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102656 | TTTTTTTTTTGAGAA[A/G]TAGTCTCCTTCCGTT | 51444 |
rs532308401 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097250 | TGGCAGAAGTAAGCT[A/T]CTATTGCAATAAAAA | 51444 |
rs532359637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32117484 | GAAATTCTTAAAGTG[A/G]CATTTGCATGCAACT | 51444 |
rs532420891 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | RNF138 | GRCh38.p7 | 18:32121138 | GAGACTGTCTCAAAA[A/C]AAAACAAAACAAAAA | 51444 |
rs532471613 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106547 | ATTATTTTTTATTTT[A/G]TTTTATTTATTTATT | 51444 |
rs532518203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117055 | TACAGGTGCCCACCA[C/T]CACGCCCAACTAATT | 51444 |
rs532593088 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32105600 | ACATGATAATATTTC[C/G]AGATGGATTGAAAAC | 51444 |
rs532642480 | in-del | -/AG | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131506 | TTTTATTGTTAAAAC[-/AG]AGTCTTATTTGAGAT | 51444 |
rs532683971 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130340 | TATGGTGCTCATTTG[G/T]TATTCTCAAATATAA | 51444 |
rs532768962 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092060 | CCATGAGCCTCGGCT[C/G]CGGCCCCGTTAGGGG | 51444 |
rs532851265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32104933 | TGAATAACTAAGAAA[A/G]TATTTGAAAAAGAAG | 51444 |
rs532911177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32120275 | TAGTTTTACTCAAAT[C/T]AGAATCATGTATGAA | 51444 |
rs532911290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32127885 | GGAGATTGAGACCAT[C/T]CTGGCTAACACGGTG | 51444 |
rs532939345 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108676 | AATTTTTGTTTTGTT[G/T]GGTTTTTAAATAGAT | 51444 |
rs533085096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32107739 | GGCCAGGCTAGTCTC[C/G]AACTCCTGACCTTGT | 51444 |
rs533192460 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32128737 | AGGCTGACCTCAAAC[G/T]CATAGGCTCAAACTG | 51444 |
rs533193737 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32116829 | ACCTCCGGTGATCCA[A/C]CTGCCTTGGCCTTCC | 51444 |
rs533194371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32095047 | GACAGTTCTGCCTGA[A/G]CAATGAATTAAAAGA | 51444 |
rs533293892 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129199 | CTGAAGGCTGTAGAC[A/G]TCTCTGCATCTTTGT | 51444 |
rs533340087 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122841 | AAACTAACTAACTAA[A/C]TAAATAAATAAAATT | 51444 |
rs533340171 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118981 | ATTTTCTTTTTATAT[C/T]ATGCCTGAGAAATTT | 51444 |
rs533403291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125426 | TCAGGATTCCAACAT[A/C]TAATGATCCTAGAAG | 51444 |
rs533484842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32095749 | ACTAAAATATAAACT[C/T]CCGTTTAATCCCCAT | 51444 |
rs533547331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32115759 | AAAACACACACACAC[A/G]CACACACACGCACGC | 51444 |
rs533571580 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32116851 | TGGCCTTCCAAAGTG[C/T]TGGGATCACAGGTGT | 51444 |
rs533622667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121708 | TTAAATGTATAGATA[C/T]GAGTTGTTTTTCTTT | 51444 |
rs533663326 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101726 | AAAATGCCATTAGTA[C/G]TATAAAAGTATATTT | 51444 |
rs533681922 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091693 | ACATCTTGACAAGAT[C/G]AAAACATTCTGGTAG | 51444 |
rs533719843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122212 | TTGCTCGCTTGGGCT[A/T]TGTGTGGAGAGATAA | 51444 |
rs533723417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32104287 | CAAAGGGCTGAGATT[A/C]CATGCATAAGCCACC | 51444 |
rs533794436 | snp | C/T | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32123813 | GCCTGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 51444 |
rs534147329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32126166 | TTGGGAGGCCAAGGC[A/G]GGAGGATTGCTTGAG | 51444 |
rs534151881 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092172 | AGGAAAGCGCTGGGC[C/T]GGGTCTCTACGAACA | 51444 |
rs534252735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125688 | CTGTAATTTAGCACT[G/T]TGGGAGGCCGAGAGG | 51444 |
rs534317186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32095335 | CCTCCATGCCTGACT[A/G]ATTTTGTTTTCTTTT | 51444 |
rs534381892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101144 | AAAGGTCCCGAGGTA[A/G]GAGGGAACATGCAGG | 51444 |
rs534531893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121987 | GATTCTCATGCCTCA[A/G]CCTCCCGAGTAGTTG | 51444 |
rs534643366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32095870 | AGAGACCTATAAATG[A/G]GTGTGATTGATATAG | 51444 |
rs534754660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122329 | GAAAGTAAACAGAAA[A/G]GAAAGATCAGCTGCT | 51444 |
rs534882998 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095849 | GGAGACTTAATAGTC[C/T]GCTGGAGAGACCTAT | 51444 |
rs534943450 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107665 | AGCTAGGATTACAGG[C/T]GTGTGCCACCATGCC | 51444 |
rs534999834 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109207 | TGCTCAGGCTGAAGT[G/T]CAGTGGCACGATCTC | 51444 |
rs535034143 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125056 | TAAAAAGGGAGATGC[A/G]TAGTGTGAGGTAATA | 51444 |
rs535157240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125449 | CCTAGAAGTGTTTCA[C/T]AGGTAAGTTATTTCA | 51444 |
rs535172594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108773 | CCCTGGACTCAAGCA[A/G]TCCTCCTGCCTTAGT | 51444 |
rs535205606 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126368 | CAAATGAGATAATAT[A/G]TTGGATATGTTGCAG | 51444 |
rs535239767 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32091004 | TGAGAGTCTCACTCT[A/G]TCGCCAGGGCTGGAG | 51444 |
rs535270581 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32097862 | TCTCACTCTGTTGCT[C/T]GGGCTATATATATGT | 51444 |
rs535284494 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | RNF138 | GRCh38.p7 | 18:32100512 | CGGAGTTTTGCTCTT[C/G]TTGGCCAGGCTGGAG | 51444 |
rs535305298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102778 | GCTGGGATTACAGGT[C/G]CGCAACACCACGCCC | 51444 |
rs535310514 | in-del | -/AAT | 0.0163368 | 0.0888905 | intron-variant | RNF138 | GRCh38.p7 | 18:32118847 | AAAAAAGAAAATAAT[-/AAT]AATAATAATAATAAT | 51444 |
rs535341096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103498 | GTGTCTGGTCTCATT[C/T]AGCATTTGATTAAAC | 51444 |
rs535421701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111595 | TCTTACTCTCTGATA[A/G]ATACATATACAGTTA | 51444 |