SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs754436 | snp | C/T | 0.494609 | 0.0516363 | intron-variant | RNF122 | GRCh38.p7 | 8:33563879 | CAGAGGATATCTGTG[C/T]ACTCCACAAGCACGA | 79845 |
rs754437 | snp | A/G | 0.499793 | 0.0101816 | intron-variant | RNF122 | GRCh38.p7 | 8:33564016 | CGTGATAAAGAGGTC[A/G]GTGGGAAGAGCATAG | 79845 |
rs1440530 | snp | A/G | 0.494526 | 0.0520291 | intron-variant | RNF122 | GRCh38.p7 | 8:33556976 | GCTTTGCTAGAAGGC[A/G]GCTACAAGAGAGGCA | 79845 |
rs3735948 | snp | C/G | 0.277334 | 0.248501 | utr-variant-3-prime | RNF122 | GRCh38.p7 | 8:33548176 | GAGTCAGCTGGCGCC[C/G]GCCAGCCTTTGTTTC | 79845 |
rs3735949 | snp | C/G | 0.159626 | 0.233093 | synonymous-codon | RNF122 | GRCh38.p7 | 8:33551383 | CTGTGCCTGGTTCCG[C/G]AGTTTGCTGGGAGAA | 79845 |
rs3735950 | snp | A/G | 0.499811 | 0.00973092 | synonymous-codon | RNF122 | GRCh38.p7 | 8:33558671 | AAAGATGCCTGTGCC[A/G]AAGATGACCATATAG | 79845 |
rs3735951 | snp | C/T | 0.489709 | 0.0709905 | synonymous-codon | RNF122 | GRCh38.p7 | 8:33558704 | GTTGAGCGGAAGGTC[C/T]TGGAAACTGATGGGT | 79845 |
rs3735952 | snp | G/T | 0.494609 | 0.0516363 | utr-variant-5-prime, upstream-variant-2KB | RNF122 | GRCh38.p7 | 8:33567028 | CGGGGGTGCCCGGGC[G/T]GCAGAAGCCCTCGGC | 79845 |
rs3832565 | in-del | -/A/AA | | | intron-variant | RNF122 | GRCh38.p7 | 8:33558786 | GGAGAGAAAAAAAAA[-/A/AA]TCATTAGGGTTGGAA | 79845 |
rs6468175 | snp | C/T | 0.481396 | 0.0946345 | intron-variant | RNF122 | GRCh38.p7 | 8:33563735 | TTCTCACCTCCTTCC[C/T]CCGCACTATTTGATG | 79845 |
rs6468176 | snp | A/C | 0.481473 | 0.0944461 | intron-variant | RNF122 | GRCh38.p7 | 8:33563737 | CTCACCTCCTTCCCC[A/C]GCACTATTTGATGTT | 79845 |
rs6984125 | snp | C/T | 0.495782 | 0.0457324 | intron-variant | RNF122 | GRCh38.p7 | 8:33560677 | catggtgtctcacgc[C/T]tgtaatcccagtact | 79845 |
rs7007586 | snp | A/T | 0.486332 | 0.08153 | intron-variant | RNF122 | GRCh38.p7 | 8:33553282 | gaggctaagagtggt[A/T]tttattcttaaatgg | 79845 |
rs7010369 | snp | C/T | 0.481396 | 0.0946345 | intron-variant, upstream-variant-2KB | RNF122 | GRCh38.p7 | 8:33565935 | CTAGGCTCACTGCAA[C/T]CTCCGCCTCCTGGGT | 79845 |
rs7015041 | snp | C/T | | | intron-variant | RNF122 | GRCh38.p7 | 8:33564598 | TTAAAGTAggctggg[C/T]gcagtggctcacgcc | 79845 |
rs7812958 | snp | G/T | 0.483126 | 0.0902898 | intron-variant | RNF122 | GRCh38.p7 | 8:33549823 | CCACTGCACTGGAAA[G/T]TACTGTCCTAGAAGA | 79845 |
rs7827826 | snp | A/C | 0.488545 | 0.074807 | intron-variant | RNF122 | GRCh38.p7 | 8:33559150 | AAAAAAAATAGAAAA[A/C]TTAGCTAGGCATGGT | 79845 |
rs7830119 | snp | A/C | 0.0170251 | 0.090679 | downstream-variant-500B | RNF122 | GRCh38.p7 | 8:33547446 | ctagtctctacaaaa[A/C]attttagaaaattag | 79845 |
rs7834354 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | RNF122 | GRCh38.p7 | 8:33557543 | tgaggcaggacaatc[A/G]ctttaacctaggagg | 79845 |
rs7835188 | snp | C/T | 0.11228 | 0.208646 | intron-variant | RNF122 | GRCh38.p7 | 8:33557369 | gcacgagggctcatg[C/T]ctgtaatcccagcac | 79845 |
rs7835315 | snp | C/T | 0.141596 | 0.225274 | intron-variant | RNF122 | GRCh38.p7 | 8:33557427 | ttgaggtcaggagtt[C/T]gagacctgcctggcc | 79845 |
rs7845224 | snp | C/T | 0.485731 | 0.0832509 | intron-variant | RNF122 | GRCh38.p7 | 8:33552439 | AAAGAAAAATGAAGC[C/T]CAAAGAAGTGAATTT | 79845 |
rs7845367 | snp | C/T | 0.486398 | 0.0813386 | intron-variant | RNF122 | GRCh38.p7 | 8:33552559 | ATAATGTGGTCTGTT[C/T]CCCTAATCAGGTGGA | 79845 |
rs9297205 | snp | C/T | 0.486984 | 0.079614 | intron-variant | RNF122 | GRCh38.p7 | 8:33549882 | CATTTGGTGATGTGG[C/T]ACTTAATACCAACTA | 79845 |
rs9297206 | snp | A/C | 0.483272 | 0.0899109 | intron-variant | RNF122 | GRCh38.p7 | 8:33550078 | AACTGGGATTACAGG[A/C]ATGTGCCACCACACC | 79845 |
rs9297207 | snp | A/G | 0.487241 | 0.0788465 | intron-variant | RNF122 | GRCh38.p7 | 8:33550143 | TCACCATGTTGGTCA[A/G]GCTGGTCTCGAACTC | 79845 |
rs9297208 | snp | A/G | 0.476574 | 0.105661 | intron-variant | RNF122 | GRCh38.p7 | 8:33559528 | AATGAAAATGAGCGC[A/G]TAAGAAAATATGCTT | 79845 |
rs9297209 | snp | C/T | 0.478104 | 0.102316 | intron-variant | RNF122 | GRCh38.p7 | 8:33559740 | TCTTTCTCCTCAAAG[C/T]ctcaatgtgtggtac | 79845 |
rs10095990 | snp | G/T | 0.494651 | 0.0514399 | intron-variant | RNF122 | GRCh38.p7 | 8:33562784 | aaaaattagctgggt[G/T]tggtgtctggcaccc | 79845 |
rs10106706 | snp | C/T | 0.496746 | 0.040204 | intron-variant | RNF122 | GRCh38.p7 | 8:33562842 | GCAGGAGAATTACTT[C/T]GACCTGGGAAGCGGA | 79845 |
rs10112135 | snp | C/T | 0.481396 | 0.0946345 | upstream-variant-2KB | RNF122 | GRCh38.p7 | 8:33567171 | TACTTCCCCCACCAG[C/T]CCCCAGGAAAACTCC | 79845 |
rs11270494 | in-del | -/GCTCAACAGCCACATGGT | | | intron-variant | RNF122 | GRCh38.p7 | 8:33549756 | CAACAGCCACATGGT[-/GCTCAACAGCCACATGGT]TTCCATATTGAATGG | 79845 |
rs11356110 | in-del | -/C | 0.493107 | 0.0583 | intron-variant | RNF122 | GRCh38.p7 | 8:33561109 | CAGTAAAGGTTACTT[-/C]CCCCCGCCAATGGGA | 79845 |
rs11374339 | in-del | -/A | 0.495407 | 0.0477027 | intron-variant | RNF122 | GRCh38.p7 | 8:33564572 | CTCTCAAAAAAAAAA[-/A]TTAAAGTAGGCTGGG | 79845 |
rs11374981 | in-del | -/A | 0.498415 | 0.0281103 | intron-variant | RNF122 | GRCh38.p7 | 8:33559319 | ATTAAAAAAAAAAAA[-/A]GAATTTAGGCAATGG | 79845 |
rs11781235 | snp | A/C | | | intron-variant | RNF122 | GRCh38.p7 | 8:33552892 | ggcagaaccccatct[A/C]tacaaaatgtacaaa | 79845 |
rs11787215 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF122 | GRCh38.p7 | 8:33559468 | GTTAAGAAATTACCT[A/C/T]TAAGCTTCACTTTGT | 79845 |
rs11985273 | snp | C/T | 0.280256 | 0.248162 | intron-variant | RNF122 | GRCh38.p7 | 8:33555846 | AAATGCTGACCACAA[C/T]GCCTGGCCTATGGAA | 79845 |
rs11985279 | snp | C/T | 0.123798 | 0.215808 | intron-variant | RNF122 | GRCh38.p7 | 8:33555898 | AAAggccgggcacgg[C/T]ggctcatgcctgtaa | 79845 |
rs11986873 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | RNF122 | GRCh38.p7 | 8:33555086 | AGGCTACAGACCAGG[G/T]CAGGGTGACGAAGGA | 79845 |
rs11987828 | snp | A/G | 0.109461 | 0.206758 | intron-variant | RNF122 | GRCh38.p7 | 8:33559613 | TCCAGAAGACAAGCC[A/G]TGCCAGGACTAGAAT | 79845 |
rs12675550 | snp | A/T | 0.277778 | 0.248452 | intron-variant | RNF122 | GRCh38.p7 | 8:33563108 | acagagtgagactca[A/T]gaaaaaaagaaaaaa | 79845 |
rs13249585 | snp | G/T | | | intron-variant | RNF122 | GRCh38.p7 | 8:33549950 | Gtttttttttttttt[G/T]gagatggagtttcac | 79845 |
rs13249882 | snp | C/T | | | intron-variant | RNF122 | GRCh38.p7 | 8:33550039 | cccagattcaagcaa[C/T]tctcctgcctcagcc | 79845 |
rs13274298 | snp | A/G | | | intron-variant | RNF122 | GRCh38.p7 | 8:33550028 | aacctgcacctccca[A/G]attcaagcaattctc | 79845 |
rs13277460 | snp | A/G | | | intron-variant | RNF122 | GRCh38.p7 | 8:33550020 | ctcactgcaacctgc[A/G]cctcccagattcaag | 79845 |
rs13277464 | snp | A/G | | | intron-variant | RNF122 | GRCh38.p7 | 8:33550027 | caacctgcacctccc[A/G]gattcaagcaattct | 79845 |
rs13277476 | snp | A/T | | | intron-variant | RNF122 | GRCh38.p7 | 8:33550037 | ctcccagattcaagc[A/T]attctcctgcctcag | 79845 |
rs13439478 | snp | C/T | 0.28052 | 0.24813 | intron-variant | RNF122 | GRCh38.p7 | 8:33554518 | CCCTCATCCTGCATA[C/T]AGATTTCAGCTCAGA | 79845 |
rs16881103 | snp | C/T | 0.097727 | 0.198275 | intron-variant | RNF122 | GRCh38.p7 | 8:33564989 | CATTTCTCCCTAAGT[C/T]TCTGTTCCATTGTCT | 79845 |
rs28405213 | snp | A/G | | | intron-variant | RNF122 | GRCh38.p7 | 8:33549232 | AACTCAAAAAAAAAA[A/G]AAGAATATCCCTACC | 79845 |
rs28666638 | snp | C/T | 0.277334 | 0.248501 | utr-variant-3-prime | RNF122 | GRCh38.p7 | 8:33547797 | ATTTTTCTTTAAATA[C/T]GTAACTTTCTCCCAC | 79845 |
rs33944286 | in-del | -/T | 0.5 | 0.000399361 | intron-variant | RNF122 | GRCh38.p7 | 8:33565381 | AAGAATGATTTTTTT[-/T]CCCCCTGTAACTAGC | 79845 |
rs33948081 | in-del | -/A | 0.499137 | 0.0207489 | intron-variant | RNF122 | GRCh38.p7 | 8:33562538 | CTCAAAAAAAAAAAA[-/A]GAAAAAGAAAAAAAA | 79845 |
rs34008040 | in-del | -/C | | | upstream-variant-2KB | RNF122 | GRCh38.p7 | 8:33568485 | ATAATCTCAAAACTT[-/C]CGGGAGGCTGAGGCG | 79845 |
rs34104851 | in-del | -/A | 0 | 0 | intron-variant | RNF122 | GRCh38.p7 | 8:33553090 | AAAAAAAAAAAAAAA[-/A]GAATGCCTCCTCTAT | 79845 |
rs34393992 | in-del | -/T | 0.375 | 0.216506 | intron-variant | RNF122 | GRCh38.p7 | 8:33559860 | TCAGGACCTACGCTG[-/T]TTTTTTTTTTTTTTT | 79845 |
rs34668538 | in-del | -/G | | | intron-variant | RNF122 | GRCh38.p7 | 8:33553844 | GGCGAGGTTCATGTT[-/G]CCTGGAGCCTCTTGA | 79845 |
rs34717661 | snp | A/G | | | upstream-variant-2KB | RNF122 | GRCh38.p7 | 8:33569122 | TAGCCACGTTGCCCA[A/G]GCTGGTCACAAACTC | 79845 |
rs34733594 | in-del | -/G | | | intron-variant | RNF122 | GRCh38.p7 | 8:33551222 | AGGGGTTTAGCCTCA[-/G]GGGAGACCCAGAGGT | 79845 |
rs34881251 | in-del | -/C | | | intron-variant | RNF122 | GRCh38.p7 | 8:33550258 | TTTAAATCCAGACTT[-/C]CCCACATCCCTACAT | 79845 |
rs35048552 | snp | C/T | | | utr-variant-3-prime | RNF122 | GRCh38.p7 | 8:33547860 | CCACCCCCTTCCATT[C/T]TGGAGATTTCGTATC | 79845 |
rs35067241 | in-del | -/A | | | intron-variant | RNF122 | GRCh38.p7 | 8:33554681 | GTGAACACAGCAACT[-/A]AAAATACCCTGATTT | 79845 |
rs35152989 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF122 | GRCh38.p7 | 8:33563919 | CAAGTCCTCTGATCA[A/G]TTTATCCCCACCAAC | 79845 |
rs35307107 | in-del | -/A | | | intron-variant | RNF122 | GRCh38.p7 | 8:33553070 | GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 79845 |
rs35370120 | in-del | -/A | | | utr-variant-3-prime | RNF122 | GRCh38.p7 | 8:33547981 | CACCCCTTTTGATCA[-/A]AAAAAAAAAAAAAAA | 79845 |
rs35706988 | in-del | -/T | | | intron-variant | RNF122 | GRCh38.p7 | 8:33558449 | AAATAGAAACACCAG[-/T]ATCCTCAGGGGCCTA | 79845 |
rs35794095 | snp | A/G | 0.0349115 | 0.127424 | upstream-variant-2KB | RNF122 | GRCh38.p7 | 8:33568874 | TTGTTACTCTTCCTT[A/G]AACATAGGCTGTGTA | 79845 |
rs35808236 | in-del | -/G | | | downstream-variant-500B | RNF122 | GRCh38.p7 | 8:33547395 | GATTGCTTGAGCCAA[-/G]GGAGTTAAAGACCAG | 79845 |
rs35873889 | in-del | -/A | | | intron-variant | RNF122 | GRCh38.p7 | 8:33553569 | GAGTGAGACTCTGGC[-/A]AAAAAATTTTTTTTA | 79845 |
rs35879627 | in-del | -/A | 0.499261 | 0.019899 | intron-variant | RNF122 | GRCh38.p7 | 8:33558785 | CCTGCAAAGGGAGAG[-/A]AAAAAAAAATCATTA | 79845 |
rs55894413 | snp | A/C | 0.481396 | 0.0946345 | intron-variant, upstream-variant-2KB | RNF122 | GRCh38.p7 | 8:33566249 | GCTACCCCCGCGCCC[A/C]GTCCCGCACGCTGCA | 79845 |
rs56787817 | snp | A/T | 0.0517044 | 0.152246 | intron-variant | RNF122 | GRCh38.p7 | 8:33553577 | CTCTGGCAAAAAAAT[A/T]TTTTTTAAATAAATA | 79845 |
rs56876057 | snp | A/G | | | intron-variant | RNF122 | GRCh38.p7 | 8:33565094 | ACAAGGGCTGGCCAA[A/G]AAAGACCAGGGGATC | 79845 |
rs57170749 | snp | A/C | 0.0425829 | 0.139564 | intron-variant | RNF122 | GRCh38.p7 | 8:33553922 | AGCCCATCCACCGTC[A/C]CCTCCCCTCCCACCT | 79845 |
rs57420007 | snp | A/T | 0.21875 | 0.248039 | intron-variant | RNF122 | GRCh38.p7 | 8:33553576 | ACTCTGGCAAAAAAA[A/T]TTTTTTTAAATAAAT | 79845 |
rs58644314 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | RNF122 | GRCh38.p7 | 8:33555163 | AGCTTTTAGCATCAT[A/G]TGGTTACTGTTCTGT | 79845 |
rs58716282 | in-del | -/A | | | utr-variant-3-prime | RNF122 | GRCh38.p7 | 8:33548006 | AAAAAAAAAAAAAAA[-/A]GGCCCCTGGGAATCA | 79845 |
rs58826918 | snp | C/T | 0.0854556 | 0.188216 | upstream-variant-2KB | RNF122 | GRCh38.p7 | 8:33567160 | CCCCTCCCTTTTACT[C/T]CCCCCACCAGTCCCC | 79845 |
rs59048631 | snp | C/T | | | intron-variant | RNF122 | GRCh38.p7 | 8:33552744 | CTTACATGCTGAACT[C/T]TGCAGGTAGCTTTAG | 79845 |
rs59074437 | in-del | -/A | 0.497907 | 0.0322805 | intron-variant | RNF122 | GRCh38.p7 | 8:33563117 | GAAAAAAAAAAAAAA[-/A]GCCTGAACCCTCCTA | 79845 |
rs59553113 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant, utr-variant-5-prime | RNF122 | GRCh38.p7 | 8:33565885 | TTAGATGGAGTTTCG[A/C]TCTTGTTGCCCAGGC | 79845 |
rs59895350 | snp | C/G | | | intron-variant | RNF122 | GRCh38.p7 | 8:33564946 | AAAGGGCGCTGCCCA[C/G]AAAGGGCAGTGTTAC | 79845 |
rs61212882 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | RNF122 | GRCh38.p7 | 8:33555124 | AAAGGAACAGGTGGT[A/G]CTCAGTAGCACCACA | 79845 |
rs61606630 | in-del | -/A | | | intron-variant | RNF122 | GRCh38.p7 | 8:33558794 | GGGAGAGAAAAAAAA[-/A]TCATTAGGGTTGGAA | 79845 |
rs61613607 | snp | A/G | | | intron-variant | RNF122 | GRCh38.p7 | 8:33551747 | ACTGAGTGTGCGGAA[A/G]TTAGACAGATATGCA | 79845 |
rs68063374 | multinucleotide-polymorphism | GGG/TGA | 0.5 | 0 | intron-variant | RNF122 | GRCh38.p7 | 8:33563737 | AACATCAAATAGTGC[GGG/TGA]GGAAGGAGGTGAGAA | 79845 |
rs71512677 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | RNF122 | GRCh38.p7 | 8:33548354 | GGAGGGAAGGTTGTA[A/G]AGAGGTAAGAGCCCG | 79845 |
rs71512678 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | RNF122 | GRCh38.p7 | 8:33568505 | AGGCTGAGGCGGGCA[A/G]ATTGCTTGAGCTCAA | 79845 |
rs71541853 | in-del | -/TTTTGG | 0.5 | 0 | intron-variant | RNF122 | GRCh38.p7 | 8:33557806 | TTAGGTTTGTTTTGG[-/TTTTGG]TTTTTTCCACTCTCA | 79845 |
rs72184063 | in-del | -/ATTA | 0.494609 | 0.0516363 | intron-variant | RNF122 | GRCh38.p7 | 8:33564392 | ATCCCCAAAAAGTAG[-/ATTA]ATTAATTAATTAATT | 79845 |
rs73604354 | snp | A/G | 0.211212 | 0.246973 | intron-variant | RNF122 | GRCh38.p7 | 8:33557358 | CCAGAGGCCGAGCAC[A/G]AGGGCTCATGCCTGT | 79845 |
rs74617653 | snp | A/G | 0.0854556 | 0.188216 | upstream-variant-2KB | RNF122 | GRCh38.p7 | 8:33567817 | CAGCTGGAGTGCAGC[A/G]GTGCAATAATAGCTT | 79845 |
rs74630292 | snp | C/T | 0.0197687 | 0.0974348 | utr-variant-3-prime | RNF122 | GRCh38.p7 | 8:33547970 | CCCCCATCCCCACAC[C/T]CCTTTTGATCAAAAA | 79845 |
rs74701655 | snp | A/G | 0.5 | 0 | intron-variant | RNF122 | GRCh38.p7 | 8:33556203 | AAAAAAAAAAAAAAA[A/G]AGAAAACCTAAGGTC | 79845 |
rs74782031 | snp | C/G | 0.0883596 | 0.190715 | intron-variant | RNF122 | GRCh38.p7 | 8:33554915 | CTCACCAGGTCAGAA[C/G]TGGGGCCTATTTTGG | 79845 |
rs75015439 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | RNF122 | GRCh38.p7 | 8:33564339 | GACTGCTTGAGCCCA[A/G]GAGTTCAAGACCAGC | 79845 |
rs75427835 | snp | C/G | 0.0854556 | 0.188216 | intron-variant | RNF122 | GRCh38.p7 | 8:33562183 | TTACATCGTTCCTAG[C/G]ATTAAGTTACTTTAA | 79845 |
rs75557466 | snp | C/G | 0.000922555 | 0.0214575 | missense | RNF122 | GRCh38.p7 | 8:33558703 | TGTTGAGCGGAAGGT[C/G]CTGGAAACTGATGGG | 79845 |
rs75806716 | snp | A/C | 0 | 0 | intron-variant | RNF122 | GRCh38.p7 | 8:33553070 | AGCAAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA | 79845 |