SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs751919 | snp | G/T | 0.368938 | 0.219895 | upstream-variant-2KB, intron-variant | CYLD, MIR3181, LOC102724907 | GRCh38.p7 | 16:50741834 | AGCTTCCCGCCTCCA[G/T]CCGCCGCTCTTCTCT | 1540 |
rs1362698 | snp | A/G | 0.198944 | 0.244731 | intron-variant, upstream-variant-2KB | CYLD, LOC102724907 | GRCh38.p7 | 16:50743391 | CAATAAGAATTTCCA[A/G]CAAATCATTTTCTCC | 1540 |
rs1420871 | snp | A/G | 0.146314 | 0.227484 | intron-variant | CYLD | GRCh38.p7 | 16:50781521 | TAAAGCTTAATGAGC[A/G]TTGGCAAGAAATATA | 1540 |
rs1420872 | snp | A/G | 0.360842 | 0.224085 | intron-variant | CYLD | GRCh38.p7 | 16:50773868 | ATCAGCTCTGAAGAA[A/G]AAGACATTCCATCAG | 1540 |
rs1420873 | snp | C/G | 0.378962 | 0.21417 | intron-variant | CYLD | GRCh38.p7 | 16:50769845 | AATTACAGAAATCGA[C/G]AGCAGATGAGTGGTT | 1540 |
rs1477176 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | CYLD | GRCh38.p7 | 16:50764544 | AAACCACTGGTAAGA[C/T]TGGTGAAGAATATAA | 1540 |
rs1548989 | snp | A/G | 0.19646 | 0.2442 | intron-variant | CYLD | GRCh38.p7 | 16:50773096 | GAGAATTTAACATCC[A/G]CAGAAATCTTGTGAA | 1540 |
rs1548990 | snp | A/G | 0.499965 | 0.00419314 | intron-variant | CYLD | GRCh38.p7 | 16:50745428 | GAGAGCTATGATCAC[A/G]CCACTGTACTCCAGC | 1540 |
rs1592639 | snp | A/C | 0.196149 | 0.244131 | intron-variant | CYLD | GRCh38.p7 | 16:50765958 | CACTTGCTGCTTCAT[A/C]TTGCACTTTTCTGTT | 1540 |
rs1990752 | snp | G/T | 0.136166 | 0.22258 | intron-variant | CYLD | GRCh38.p7 | 16:50759481 | TTGTTTAGCTACAGA[G/T]ATATAATTAAATTAT | 1540 |
rs2066851 | snp | A/G | 0.371177 | 0.218669 | intron-variant | CYLD | GRCh38.p7 | 16:50765018 | TTGCAGGGATAACCA[A/G]TTCTATGCTAATATT | 1540 |
rs2066852 | snp | C/T | 0.156341 | 0.231793 | synonymous-codon, nc-transcript-variant, intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50793607 | TAGAGAATGCTACGA[C/T]GATCCGGACATCTCA | 1540 |
rs2111435 | snp | A/G | 0.499354 | 0.0179596 | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50785999 | TTCAGAGGAGAACTT[A/G]GCGGCTACCATAAGT | 1540 |
rs2160683 | snp | A/T | 0.391583 | 0.206044 | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50795942 | CTGTCCAATTTGGAA[A/T]AGATCTAGTCAAATG | 1540 |
rs2216313 | snp | A/T | 0.201418 | 0.245234 | intron-variant, upstream-variant-2KB | CYLD, LOC102724907 | GRCh38.p7 | 16:50743545 | GACTATAAAAATCAT[A/T]GCTGCTTAATGTTAG | 1540 |
rs2302759 | snp | C/T | 0.336052 | 0.234732 | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50793690 | TGTTCAACAAAAGTT[C/T]ATCCATTAAGTGAAG | 1540 |
rs2302760 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CYLD | GRCh38.p7 | 16:50782092 | ACACACTTTAGAGTA[C/T]TATGTGTAAAAAGCA | 1540 |
rs3064634 | in-del | -/ACAC/ACACAC/ACACACACACAC/CA | 0.625 | 0.125 | upstream-variant-2KB, intron-variant | CYLD, MIR3181, LOC102724907 | GRCh38.p7 | 16:50741064 | CACACACACACACAC[-/ACAC/ACACAC/ACACACACACAC/CA]CCCTCCTCCTTTCTC | 1540 |
rs3064635 | in-del | -/T/TT | 0 | 0 | intron-variant | CYLD | GRCh38.p7 | 16:50767480 | ATTTTTTTTTTTTTT[-/T/TT]AATTTCCATAGAGTA | 1540 |
rs3064638 | in-del | -/ACACAC | | | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50793138 | cacacacacacacac[-/ACACAC]acacaTGCATATATA | 1540 |
rs3135501 | snp | A/G | 0.5 | 0.000399361 | intron-variant | CYLD | GRCh38.p7 | 16:50756788 | CAAACTTATAATGTA[A/G]GTCTTAATGATCCCC | 1540 |
rs3135502 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | CYLD | GRCh38.p7 | 16:50757094 | CACAATTGAATAAGC[A/C]AACTGAATTGTTTTT | 1540 |
rs3135503 | snp | G/T | 0.327445 | 0.237702 | intron-variant | CYLD | GRCh38.p7 | 16:50757339 | ATAGGATTCAAATGA[G/T]AGCTTTATTTCAATT | 1540 |
rs3743781 | snp | C/T | 0.108402 | 0.206034 | utr-variant-3-prime, nc-transcript-variant, intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50797345 | AAATTCATTTTCTTA[C/T]GGACTGTATGTTTGT | 1540 |
rs3743782 | snp | A/C | 0.104149 | 0.203046 | upstream-variant-2KB, intron-variant | CYLD, MIR3181, LOC102724907 | GRCh38.p7 | 16:50741910 | CAGCCCGGCGCCGGC[A/C]GAAGGGACTTTCCGC | 1540 |
rs3785140 | snp | A/G | 0.378568 | 0.214407 | intron-variant | CYLD | GRCh38.p7 | 16:50783133 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCCGT | 1540 |
rs3785141 | snp | C/T | 0.104149 | 0.203046 | intron-variant | CYLD | GRCh38.p7 | 16:50783028 | ctgagtcaagagaat[C/T]gcttgaacctgggag | 1540 |
rs3785142 | snp | C/T | 0.499913 | 0.00658888 | intron-variant | CYLD | GRCh38.p7 | 16:50753236 | AAAAGGAGTGCTTTA[C/T]TGTCAGCTATCCTGA | 1540 |
rs4027241 | snp | A/G | 0.49655 | 0.04139 | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50785655 | GGATCCTATTGTTCA[A/G]CCAGTTAAGAATCAT | 1540 |
rs4785226 | snp | A/C | 0.49995 | 0.00499176 | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50789053 | ACAAAATGAAGTGGG[A/C]AAAAATCTTGAAGAA | 1540 |
rs4785450 | snp | C/T | 0.359998 | 0.2245 | intron-variant | CYLD | GRCh38.p7 | 16:50758357 | gaaagttgtaggagc[C/T]gcagtgggagctgga | 1540 |
rs4785451 | snp | A/G | 0.499839 | 0.00898417 | intron-variant | CYLD | GRCh38.p7 | 16:50774391 | AGTACTGAACCCTAC[A/G]TATACTGTGTTTTTC | 1540 |
rs5816719 | in-del | -/AC/ACAC/ACACAC/ACACACAC | 0.478104 | 0.102316 | upstream-variant-2KB, intron-variant | CYLD, MIR3181, LOC102724907 | GRCh38.p7 | 16:50741030 | GTGTCATGATTAAAA[-/AC/ACAC/ACACAC/ACACACAC]ACACACACACACACA | 1540 |
rs5816721 | in-del | -/A | | | intron-variant | CYLD | GRCh38.p7 | 16:50768352 | TCTTTTCTTGAGGGG[-/A]AAAAAAAGTCAAAGT | 1540 |
rs6145827 | in-del | -/ACACAC | | | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50793116 | CAAAAGGAGCCATAT[-/ACACAC]ACACACACACACACA | 1540 |
rs6500329 | snp | A/G | 0.3746 | 0.216737 | intron-variant | CYLD | GRCh38.p7 | 16:50770520 | tagtggcgtgatctc[A/G]gctcactgtaacctc | 1540 |
rs6500331 | snp | A/G | 0.486529 | 0.0809556 | intron-variant | CYLD | GRCh38.p7 | 16:50774815 | TGGGTAACTGATACC[A/G]TGGAAGGTAAAAGTG | 1540 |
rs6500332 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CYLD | GRCh38.p7 | 16:50779241 | TAATTTAGCCATGTT[C/T]CACAAGGAttctttc | 1540 |
rs7184210 | snp | C/T | 0.0998734 | 0.199905 | downstream-variant-500B, intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50802362 | ggagtctcgctctgt[C/T]gccccagttggagtg | 1540 |
rs7187352 | snp | A/G | 0.107694 | 0.205546 | intron-variant | CYLD | GRCh38.p7 | 16:50749517 | CAGTCATGTAGAATG[A/G]AGTCTAAAGTTTATT | 1540 |
rs7192397 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | CYLD | GRCh38.p7 | 16:50782239 | ATACAAAAACATTTT[A/G]AAATGAAAAAATATT | 1540 |
rs7194167 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50793898 | CATTCACTTGACACA[C/T]TGAGTTTCTCTCATT | 1540 |
rs7195766 | snp | C/T | 0.280785 | 0.248097 | intron-variant | CYLD | GRCh38.p7 | 16:50745984 | AGCATATTTTTATTG[C/T]AATACTGGTATTTTG | 1540 |
rs7197362 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | CYLD | GRCh38.p7 | 16:50754909 | tatacatataCAcac[A/T]tatatgtatacatat | 1540 |
rs7198188 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | CYLD | GRCh38.p7 | 16:50748046 | GTTGTTTGATCATTA[A/C]GTGATTAAATCTAAA | 1540 |
rs7199842 | snp | C/T | 0.0244538 | 0.107838 | intron-variant, upstream-variant-2KB | CYLD, LOC102724907 | GRCh38.p7 | 16:50743286 | GCTTTCTACACACCC[C/T]CTCACGCCCCAAGTA | 1540 |
rs7200370 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50788804 | tctgtataccttcaa[A/G]caaatatgaaaaagt | 1540 |
rs7200535 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | CYLD | GRCh38.p7 | 16:50752075 | CTTGCAAATTGAACA[C/G]TTTGAATATTTAACA | 1540 |
rs7342715 | snp | A/G | 0.499995 | 0.00159744 | intron-variant | CYLD | GRCh38.p7 | 16:50753572 | TCTATTATAGTCCTT[A/G]AGAGGAAAGTTCTGG | 1540 |
rs7342808 | snp | A/G | 0 | 0 | intron-variant | CYLD | GRCh38.p7 | 16:50753370 | TCTCCCCTTGCATCA[A/G]GCTCTTTACCTTGGG | 1540 |
rs7500289 | snp | C/T | 0.196149 | 0.244131 | intron-variant | CYLD | GRCh38.p7 | 16:50770599 | gggattacaggtgtg[C/T]gcccccgagcccagc | 1540 |
rs8047910 | snp | A/G | 0.508281 | 0.0444513 | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50785201 | TTTGTTCATTCAGGA[A/G]TATAGAGAGAAAGTG | 1540 |
rs8053457 | snp | A/G | 0.5 | 0.000399361 | intron-variant | CYLD | GRCh38.p7 | 16:50770376 | gtgattttgatttga[A/G]tttacctgatggctg | 1540 |
rs8060598 | snp | C/T | 0.388587 | 0.208071 | intron-variant | CYLD | GRCh38.p7 | 16:50747891 | AGGAGGTGCCTAACC[C/T]GTATCCTGTCTTGGC | 1540 |
rs8060765 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, intron-variant | CYLD, LOC102724907 | GRCh38.p7 | 16:50740107 | ggccgggcacattgg[C/T]tcatgcctgtaatcc | 1540 |
rs8061821 | snp | A/C | 0.413582 | 0.189052 | intron-variant, downstream-variant-500B | CYLD, LOC105371251 | GRCh38.p7 | 16:50783638 | CCACCTCCCGGGTTC[A/C]AGCGATTCTCCTATC | 1540 |
rs8062105 | snp | C/T | 0.378568 | 0.214407 | intron-variant | CYLD | GRCh38.p7 | 16:50761983 | ctttctattctgtCT[C/T]CCCACGTTTCAATAC | 1540 |
rs8062540 | snp | A/G | 0.413748 | 0.188909 | intron-variant, nc-transcript-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50784021 | GTAGTCTCTCTATCA[A/G]CTTTTGCAAAGAAGT | 1540 |
rs9646285 | snp | C/T | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant, intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50798843 | TGGAGCTTGACGTCT[C/T]TTTAATGTTACTTGG | 1540 |
rs9925070 | snp | G/T | 0.326035 | 0.238157 | intron-variant | CYLD | GRCh38.p7 | 16:50766736 | TTGAGGGACTGAAGA[G/T]TTCAGTGGAAAAAAT | 1540 |
rs9938976 | snp | A/G | 0.334182 | 0.235401 | intron-variant | CYLD | GRCh38.p7 | 16:50783308 | ATTGTAGACTGGGCT[A/G]AATTGAGAGTAGCCT | 1540 |
rs9940175 | snp | C/T | 0.362941 | 0.223034 | intron-variant | CYLD | GRCh38.p7 | 16:50746641 | TTAGGAAAAAAGTTA[C/T]CACTCCTTGTAGAGT | 1540 |
rs10451132 | snp | G/T | 0.231482 | 0.249313 | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50792551 | TTCATAGGGAAAAGT[G/T]TTTTTTTTAACACTT | 1540 |
rs11271535 | in-del | -/ACACACATATATAT | | | intron-variant | CYLD | GRCh38.p7 | 16:50752004 | TACACACATATATAT[-/ACACACATATATAT]GTATAGTTTATATAT | 1540 |
rs11644525 | snp | A/G | 0 | 0 | intron-variant | CYLD | GRCh38.p7 | 16:50775177 | ACAGCTTTATCAGGT[A/G]TGACTCCTAAGTGTC | 1540 |
rs11646600 | snp | A/G | 0 | 0 | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50790808 | CTAACTTTATATCCA[A/G]AAATTCTGCTGAAAA | 1540 |
rs11859047 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | CYLD | GRCh38.p7 | 16:50763283 | gtagatagatattta[C/G]gtttttttttcacct | 1540 |
rs11859674 | snp | A/G | 0.378765 | 0.214288 | intron-variant | CYLD | GRCh38.p7 | 16:50768804 | TTTGACGATCTCTAC[A/G]ATCAAGATAGTGAAC | 1540 |
rs11861521 | snp | C/T | | | intron-variant | CYLD | GRCh38.p7 | 16:50757802 | cggcctcccaaagtg[C/T]tgggactacaggcgt | 1540 |
rs11862710 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | CYLD | GRCh38.p7 | 16:50758735 | gtttggactgagcaa[C/T]tggtaggctggagag | 1540 |
rs11862720 | snp | C/G | 0.382085 | 0.212258 | intron-variant | CYLD | GRCh38.p7 | 16:50758793 | aggaagagcatgcgt[C/G]ggggagtgggagttg | 1540 |
rs11863544 | snp | G/T | 0.196149 | 0.244131 | intron-variant | CYLD | GRCh38.p7 | 16:50766782 | ggaagtagcaaaaga[G/T]ctagaactagaggtg | 1540 |
rs11863594 | snp | A/G | 0.382085 | 0.212258 | intron-variant | CYLD | GRCh38.p7 | 16:50763403 | ggagtggaattgctg[A/G]gtcatatgataactc | 1540 |
rs11863916 | snp | G/T | 0.204496 | 0.245824 | intron-variant | CYLD | GRCh38.p7 | 16:50767791 | TAGAGCTGTATTTCC[G/T]TCTGTCTATTTTTTC | 1540 |
rs11864090 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | CYLD | GRCh38.p7 | 16:50760374 | CAAAATTAAAAAGTA[A/C]AATAAAATATCTCAT | 1540 |
rs11864698 | snp | A/G | 0.381891 | 0.212379 | intron-variant | CYLD | GRCh38.p7 | 16:50764296 | ttccttgactatttg[A/G]caaaGCTTCTTTTTG | 1540 |
rs11865799 | snp | A/G | 0.0323874 | 0.123064 | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50791548 | TATTTTTTTCTCTGC[A/G]TGTTTTTAGATCAGC | 1540 |
rs11866167 | snp | A/C | 0.100944 | 0.200705 | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50792039 | TATAATGTTTACTTC[A/C]CCCCTTCATTAAGAG | 1540 |
rs12324931 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | CYLD | GRCh38.p7 | 16:50756247 | CTTAGTGGGGGAAAA[A/C]CCCTTCCTGTTAATT | 1540 |
rs12444259 | snp | A/G | | | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50793972 | agagactaatgccca[A/G]gctggagtgcagtgg | 1540 |
rs12597446 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | CYLD | GRCh38.p7 | 16:50782982 | caggctggaatgcag[C/T]ggcacaatctgggct | 1540 |
rs12599808 | snp | A/G | 4.9708e-05 | 0.00498513 | missense, nc-transcript-variant | CYLD | GRCh38.p7 | 16:50751617 | AGGAAGAAGGTCGTG[A/G]TCAAGGTTTCACTGA | 1540 |
rs12599914 | snp | A/G | 0.0334203 | 0.124873 | intron-variant, downstream-variant-500B | CYLD, LOC105371251 | GRCh38.p7 | 16:50787056 | TTTTCTTTTAAATTA[A/G]AAATTTCTTTTTATG | 1540 |
rs12924216 | snp | A/T | | | intron-variant | CYLD | GRCh38.p7 | 16:50772191 | ctttggttggggcct[A/T]cttttgtctatgcct | 1540 |
rs12929222 | snp | A/G | 0.417034 | 0.18601 | intron-variant | CYLD | GRCh38.p7 | 16:50755139 | tatatatacacacgt[A/G]tacatatgtgtgtat | 1540 |
rs12929234 | snp | A/G | 0.0798611 | 0.183174 | intron-variant | CYLD | GRCh38.p7 | 16:50755151 | cgtgtacatatgtgt[A/G]tatataCACACgtgt | 1540 |
rs12930153 | snp | C/T | | | intron-variant | CYLD | GRCh38.p7 | 16:50755084 | atgtatacatataca[C/T]acatatatacataca | 1540 |
rs12933741 | snp | A/G | 0 | 0 | intron-variant | CYLD | GRCh38.p7 | 16:50767778 | CACACACACACTCTA[A/G]AGCTGTATTTCCTTC | 1540 |
rs12933742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CYLD | GRCh38.p7 | 16:50767780 | CACACACACTCTAGA[A/G]CTGTATTTCCTTCTG | 1540 |
rs12934597 | snp | C/T | | | intron-variant | CYLD | GRCh38.p7 | 16:50755078 | atagatatgtataca[C/T]atacacacatatata | 1540 |
rs12934724 | snp | C/T | | | intron-variant | CYLD | GRCh38.p7 | 16:50755120 | acacacatatacaca[C/T]gtgtatatatacaca | 1540 |
rs12934730 | snp | C/T | | | intron-variant | CYLD | GRCh38.p7 | 16:50755126 | atatacacatgtgta[C/T]atatacacacgtgta | 1540 |
rs13333006 | snp | A/G | | | intron-variant | CYLD | GRCh38.p7 | 16:50783115 | tttgtattttcagta[A/G]agacgggggtttcac | 1540 |
rs13336419 | snp | C/T | 0 | 0 | intron-variant | CYLD | GRCh38.p7 | 16:50752958 | GTATAAAGAAGGAAA[C/T]TCATATGGAATTACT | 1540 |
rs13337656 | snp | C/T | 0.409212 | 0.192748 | intron-variant | CYLD, LOC105371251 | GRCh38.p7 | 16:50786495 | CCAGGTGTGGTGGCG[C/T]ACACCTGTAATCCCA | 1540 |
rs13338860 | snp | A/C | 0.00331296 | 0.0405648 | CYLD, LOC105371251 | 16 | allele_origin=A(germline)/C(germline) | 16:50786996 | TGAAGAGCATATTCA[A/C]ATGTCAAAGTATTAG | 1540 |
rs16948789 | snp | A/G | 0.0240643 | 0.107019 | upstream-variant-2KB, nc-transcript-variant | CYLD, MIR3181, LOC102724907 | GRCh38.p7 | 16:50740777 | TTATGGCTTCCTACA[A/G]CAGTGTGGTCATGAA | 1540 |
rs16948792 | snp | C/T | 0.2776 | 0.248472 | intron-variant | CYLD | GRCh38.p7 | 16:50762471 | CTTTCTGAGCCCTGT[C/T]ATTTCCCTACACTAA | 1540 |
rs16948808 | snp | A/T | 0.19646 | 0.2442 | intron-variant | CYLD | GRCh38.p7 | 16:50773615 | ATATCTTTAATCAGG[A/T]TTGTTTTAATCACAC | 1540 |
rs16948810 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | CYLD | GRCh38.p7 | 16:50776954 | CATTGGGGCCTGGGA[C/G]ACTTAGGATTAATTG | 1540 |