SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs752151093 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119001062 | GCTATTGTTTACTCC[A/G]TCACTGTAACAATGT | 79836 |
rs752151426 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118978219 | AAATAGAGCCTAACC[C/T]TTTTGATCTCCAGTA | 79836 |
rs752216279 | snp | C/T | 0.000489237 | 0.0156326 | intron-variant, synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118987026 | TAGATTAAAGGAAAA[C/T]GTAGAGTCAATGACT | 79836 |
rs752221283 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119004136 | CATTTTTTTTCTTGC[C/T]TTAGTGCACTGAGAC | 79836 |
rs752241740 | snp | A/G | 1.68667e-05 | 0.00290397 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975240 | GCCACCGAGGTGTGG[A/G]ACGGCTTTAAGTGCC | 79836 |
rs752297485 | snp | C/G | 2.28321e-05 | 0.00337869 | missense, nc-transcript-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006216 | CAAAGTGTCCATTGT[C/G]CAAAGACGGTCTTTC | 79836 |
rs752311059 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119002618 | TGCTTATAAGTGTTT[A/G]TTCATTTTCTGTTCG | 79836 |
rs752312447 | snp | A/T | 0.0343555 | 0.126481 | intron-variant | LONRF3 | GRCh38.p7 | X:119000816 | CTCTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC | 79836 |
rs752313894 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988030 | GTTGAGGATCAGAAG[C/T]GCAGACTCCAAGGCA | 79836 |
rs752318586 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119010968 | AAATTACAAAAATTA[A/G]CCAGGCATGGTGGCA | 79836 |
rs752334502 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973107 | GGGACCTTGGTGTTG[A/G]TCTAAGACTGGTTTA | 79836 |
rs752345067 | snp | C/T | 2.28412e-05 | 0.00337936 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118990500 | AGGGGGACAAACCTG[C/T]TCTCAGTTTACCACT | 79836 |
rs752405001 | snp | C/G | 0.000236518 | 0.0108721 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975125 | CCTGGCGGAGAAAGT[C/G]CCGCAAGGCGAGGCG | 79836 |
rs752486233 | snp | A/C | 0.000522534 | 0.0161553 | intron-variant, missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118987051 | ATGACTACTGAAGTT[A/C]CCAGCCATAATCTAC | 79836 |
rs752487530 | snp | G/T | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012352 | TACAATAATAGTACC[G/T]ACCTCATTGGGTTTG | 79836 |
rs752537596 | snp | A/G | 4.56913e-05 | 0.00477949 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989458 | GGAAGCAGCAGCCAG[A/G]GGAGATGGCAGCAGT | 79836 |
rs752565360 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979791 | TAGTCAGTCAGCCTG[C/T]CAGTATCCCCAAGGA | 79836 |
rs752570600 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118989339 | TTCCCTTTGTTCCTC[C/T]GGGTAGGAATATGAG | 79836 |
rs752576490 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977255 | ATATGAATGAGGCAG[A/G]TGGAGGTCACTTAAC | 79836 |
rs752595914 | in-del | -/T | 0.000529661 | 0.016265 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018592 | TTTACTTCAGCAATC[-/T]TAATTGTACGTGTAT | 79836 |
rs752645595 | snp | C/T | 2.2915e-05 | 0.00338482 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014314 | AAAGAATCGGATACT[C/T]AATCACTTTGGTCCC | 79836 |
rs752674701 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118997212 | CATCAAACTATCTGA[C/T]TTCAAACTATACTAT | 79836 |
rs752690523 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118997852 | AGAAGATACACAAAT[G/T]GCCAACAAACATAAA | 79836 |
rs752734813 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119004329 | CTCTCCTCCTCCAGA[C/T]CTCCATTGGCTTGTT | 79836 |
rs752786147 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119003382 | TTATTTTTACAGCCC[A/C]CATGGAATTGATTTT | 79836 |
rs752801803 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118983192 | AGGAATGTTCTTGCT[A/T]CTTTGACTCAGGGTC | 79836 |
rs752822111 | snp | A/G | 2.56325e-05 | 0.00357989 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119012908 | TGTAATTGAAGCTGT[A/G]ACCCAGGGACAGGAA | 79836 |
rs752899376 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118982449 | CTGGGCAGGCCCTGA[A/C]AGCTGGTTAGCATGT | 79836 |
rs752925688 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119007125 | AGTAGGGAAATTAAT[G/T]TGTGTTGGAAACGAA | 79836 |
rs752943876 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013650 | TCCCAATAATCCATC[A/G]TCCCCTAAGGCAGAA | 79836 |
rs752981741 | snp | C/T | 2.29229e-05 | 0.0033854 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011962 | CATGTGCCTTGGAGA[C/T]CCTGTCAAAGGGTAA | 79836 |
rs753000900 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118983217 | AGGGTCTGGATTGTC[A/G]GTGGGAGAAAAACCA | 79836 |
rs753026105 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118991962 | ATAGATGTATTAATG[G/T]CTCGAAGTTGTATGT | 79836 |
rs753114046 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119008984 | AATACATATATTATG[A/G]TGGTAACAGCTGCTA | 79836 |
rs753114644 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:119000056 | GCTTCAGCTTGAATT[A/T]TGATAGCCTTGACAA | 79836 |
rs753121939 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118990230 | ATTTGAATGAAGTCC[C/T]CAGGGCTCCTGGACA | 79836 |
rs753173597 | in-del | -/TAAATCAATATTTCTTTCTTGTTTGGTT | 2.29621e-05 | 0.00338829 | splice-donor-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006237 | ACGGTCTTTCACAGG[-/TAAATCAATATTTCTTTCTTGTTTGGTT]TAAATCAGTATTTCT | 79836 |
rs753186661 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979158 | GGCGCCCGCCACCAC[A/G]CCTGGCTAATTTTTT | 79836 |
rs753186863 | snp | A/C | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118978799 | CAAATGACTTAACTT[A/C]CCAGTACTTCATCTC | 79836 |
rs753226671 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119007962 | GTGCCTTTTCTGGCT[C/T]TTTGTTTTAGTATCA | 79836 |
rs753250444 | snp | A/C | 2.27959e-05 | 0.00337601 | synonymous-codon, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982830 | TTCCAGGCACATTTC[A/C]GAAAAGCCCAAGCCT | 79836 |
rs753336659 | snp | A/G/T | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:119016503 | CAGAAGCCCGCCACC[A/G/T]CGCCCGGCTAATTTT | 79836 |
rs753352655 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119001357 | AAGATGGGCTTGAGA[A/G]TCAGATCTGACCTGA | 79836 |
rs753427734 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002178 | GATACTTATGTAACC[C/T]CTCTCAGTTCAAGAA | 79836 |
rs753442016 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119002392 | TATCCAGAATTTATT[A/G]TTTCAATCTGGCTTC | 79836 |
rs753451025 | snp | C/G | 3.76854e-05 | 0.00434065 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975063 | TATAGACAGCTCTCC[C/G]AGCGGCAGCAGCTGG | 79836 |
rs753459492 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119006916 | TTTAGTAGAAATGGG[G/T]TTTCACCATATTGGT | 79836 |
rs753486024 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974395 | CCCCACCCCACAACC[C/T]CACTTCCGAAAAAGA | 79836 |
rs753504991 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118985265 | ACTGAAGAGTATTAT[G/T]CTCTTTTTGGGAGAA | 79836 |
rs753535337 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118985732 | TACTGTGTAGAACAG[A/G]ACTGGAATAGTGAGG | 79836 |
rs753561523 | snp | C/G | 2.97814e-05 | 0.00385873 | intron-variant | LONRF3 | GRCh38.p7 | X:118989676 | CCTCCAAGCAAGGTA[C/G]TGGCTCTACCCAGAG | 79836 |
rs753567396 | in-del | -/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003665 | TCTGGTAGAGTGAGT[-/C]CTCCCACATCGTTGC | 79836 |
rs753631329 | in-del | -/A | 0.00215285 | 0.0327382 | intron-variant | LONRF3 | GRCh38.p7 | X:119011113 | AGTGAGACTCCGCTT[-/A]AAAAAAAAAAAAAAA | 79836 |
rs753640604 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986837 | AGTTCTGCCCTGCAA[C/G]CTGGCTCCCTCCCCC | 79836 |
rs753717290 | snp | A/C | 2.29066e-05 | 0.0033842 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989482 | CAGCAGTCTGATGGA[A/C]CCAGCTAAAGTGAAG | 79836 |
rs753721828 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118981209 | ATATGGGTTGGCCGG[C/G]CATGGTGGCTTACTC | 79836 |
rs753828649 | snp | C/G | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012118 | TAAGGATCATTGTCC[C/G]TTTGGTGGTTAGTTT | 79836 |
rs753861329 | snp | G/T | 0.000153527 | 0.00876014 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975210 | GAAGAGACGGGGGCC[G/T]CCGCGGCTGCGGCGG | 79836 |
rs753864318 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118990302 | ACCTCTGAGAGCCTA[C/T]TTCTGAGTGTCCCAT | 79836 |
rs753874343 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119005557 | CCCCTATGAAAATTA[C/T]CTATATAAAAGGCAG | 79836 |
rs753877400 | in-del | -/A | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118997963 | CATAATAAAAAACTC[-/A]AAAAAACAGTAGATG | 79836 |
rs753905470 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118997321 | GAAATAAACCCAAAT[A/G]CTTACAGCCAACTGA | 79836 |
rs753941373 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118997589 | CGAGAACCGAAAAGC[A/G]AATGCAATAAAAACA | 79836 |
rs753995679 | in-del | -/AA | | | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119019136 | GCAAACCTGCGTCTC[-/AA]AAAAAAAAAAAAAAA | 79836 |
rs753996958 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976647 | GTAACGTGGGCAGTC[C/T]CCCATCTCCAGCTAG | 79836 |
rs754025842 | snp | C/T | 6.95281e-05 | 0.0058957 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014245 | GCTCATGGGATTACA[C/T]AACTGTGTCTATCAG | 79836 |
rs754032106 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118996549 | GAGTCAAATCAAGAT[C/T]CCCTTTTACAATAGC | 79836 |
rs754051637 | in-del | -/GGGAGATGGCAGCAGTCTGATGGACCCAGCTAAAGTGAA | 2.2848e-05 | 0.00337986 | cds-indel, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989457 | GGAAGCAGCAGCCAG[lengthTooLong]GGGAGATGGCAGCAG | 79836 |
rs754082178 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118984152 | AGGTTTGGTTAGTTA[G/T]CCTCAGGTTACAGGT | 79836 |
rs754115030 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118980817 | GATAGTGTGGTGAGA[A/C]GCAGAGCTGAGAAGC | 79836 |
rs754115275 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119007040 | ATTTCTCCTGTCTTA[C/T]AGCCACTGTCCCCCT | 79836 |
rs754123046 | snp | C/T | 1.67267e-05 | 0.0028919 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974751 | TCCCCGGTCCCTAGA[C/T]GCCTCGTCTCCTCCC | 79836 |
rs754280479 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119004821 | TTTTATGTCAATTTT[A/G]CATCAGTAAAGCTGT | 79836 |
rs754286046 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979579 | ACAGGTGTGAGCCAC[C/T]GTGTCCAGCCTATAT | 79836 |
rs754370988 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972926 | GACTACATCTGGAGT[C/T]TCTCTATTTCTTCTT | 79836 |
rs754381379 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118985358 | GAGGACCAACCTTGG[C/T]TCCTGTGGAGGAGGG | 79836 |
rs754436470 | snp | A/T | 0.0440191 | 0.141675 | intron-variant | LONRF3 | GRCh38.p7 | X:119000814 | CTCTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC | 79836 |
rs754440075 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119002446 | CCATGTTATTGCATA[C/T]AGGTAAAGTTTGTTC | 79836 |
rs754443495 | snp | A/G | 0.00370173 | 0.0428621 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973001 | TCTTTTTTCCCCTAT[A/G]TGATGCTTCCTTTCT | 79836 |
rs754473014 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119001496 | ACCACCTCTTAATAT[A/G]CAAAGTTAAGTATTG | 79836 |
rs754501391 | in-del | -/A/CA | 0.497488 | 0.0353502 | intron-variant | LONRF3 | GRCh38.p7 | X:118993129 | CTAACACCCCCCCCC[-/A/CA]AAAAACCACACTAGT | 79836 |
rs754561405 | snp | C/G | 5.87469e-05 | 0.00541941 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975086 | GCAGCTGGTGGCTGA[C/G]CAGCTGGAGCAGCTG | 79836 |
rs754637475 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979686 | GGTGCTCCTGAACCT[C/T]TACTGATAGGCTCCT | 79836 |
rs754650572 | in-del | -/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119004107 | ACAGATTTGTTTTTT[-/T]CCTCTCCAGTTCTCA | 79836 |
rs754665973 | snp | C/T | 3.29777e-05 | 0.00406051 | intron-variant | LONRF3 | GRCh38.p7 | X:118989680 | CAAGCAAGGTACTGG[C/T]TCTACCCAGAGAGAA | 79836 |
rs754666436 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119000296 | GTAGAAAAACAAGTT[A/G]GAGTATGAATTTGTA | 79836 |
rs754721090 | snp | A/G | 2.28898e-05 | 0.00338296 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118990482 | CAGATCCTCCCACTG[A/G]TCAGGGGGACAAACC | 79836 |
rs754736079 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119008475 | GTGACAATTGAGCCT[C/G]AGTCCAGTTCTTGAA | 79836 |
rs754836117 | snp | C/T | 2.27941e-05 | 0.00337587 | synonymous-codon, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982875 | AAGGTGGAGGAGGCA[C/T]TAAGGGAGTTTCTCT | 79836 |
rs754903903 | snp | A/C/G | 9.37732e-05 | 0.00684683 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119013003 | AAACAGAACTCATCA[A/C/G]GGATCTAGTCTCTCG | 79836 |
rs754934080 | snp | C/T | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012120 | AGGATCATTGTCCCT[C/T]TGGTGGTTAGTTTAC | 79836 |
rs754946188 | snp | C/G | 0.00581083 | 0.0535878 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974715 | CCCCGATTTCCTCCA[C/G]CTGCCACTCCTTGCT | 79836 |
rs754966281 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017788 | ATATCTTAACAGAAG[A/G]GGGTGTCAAACAGAG | 79836 |
rs754982747 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118982411 | GTTCTCTGCTTGAGA[G/T]ACTAGTTCAAACGAA | 79836 |
rs755046599 | snp | C/T | 3.42477e-05 | 0.00413796 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975455 | GCCGCCGCTGCGAGT[C/T]AACGTGGTGCTCAGC | 79836 |
rs755048937 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981314 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 79836 |
rs755121081 | snp | C/T | 2.27915e-05 | 0.00337568 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011899 | CTTTGAGCCTTGTTA[C/T]CGCCTGATGATTCGT | 79836 |
rs755126415 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005008 | GACCTCAGGTTCATT[A/C]TAGTTAGTGGGTTCA | 79836 |
rs755141537 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975694 | GGGATTTGGACCAGG[G/T]CAGAAGAGGGGGCGG | 79836 |
rs755153365 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:119003235 | TTATTTGAGACATGG[A/G]GTGTCAAACTCCTGG | 79836 |
rs755161622 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118995477 | CCCAGCAGAATAAAG[A/G]AAATAACCAAGATCA | 79836 |
rs755201420 | in-del | -/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118993952 | TGAAGGAAAGATAGA[-/C]ATTTTCAGACAAACA | 79836 |
rs755207910 | snp | G/T | 2.45441e-05 | 0.00350306 | intron-variant | LONRF3 | GRCh38.p7 | X:119009290 | TTCACTCATACCAGC[G/T]CAATGAGAGCTGAAT | 79836 |
rs755257580 | in-del | -/CAG | 3.29457e-05 | 0.00405854 | cds-indel, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989507 | GTGAAGGGGGATGGT[-/CAG]CAGCACCACATGAAA | 79836 |
rs755307189 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118989836 | TGCTATGAGGCTTCT[A/G]TGAGATCATGTACAG | 79836 |
rs755319363 | snp | A/G | 4.68972e-05 | 0.00484215 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017677 | TGGCCTTCATATCCC[A/G]AAACCAAAACTAGTG | 79836 |
rs755324520 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988428 | ACTCCTGAGTGGCCA[A/G]TGCCTTGGGTTCATG | 79836 |
rs755327495 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118978712 | TGACTCTCTAGAATA[C/T]GCACTTGGGAGCCAG | 79836 |
rs755352141 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118998806 | TCCCAGTTCAGGCAA[C/T]TCAGCCTCCTGCCTG | 79836 |
rs755360965 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119007068 | CCTCTCCATAAAGTC[C/G]TTCAGGAAAATGAGG | 79836 |
rs755372985 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118990889 | TGGAGACAGAGTCTT[A/G]CTCTGTTGCCCAGGC | 79836 |
rs755387600 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119005936 | AACTTTAATAAATGT[A/G]TTTTAATCCAGCTCA | 79836 |
rs755414505 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118978240 | ATCTCCAGTAGAAAA[A/G]TCCTAGAAAACTTAT | 79836 |
rs755456386 | snp | A/G | 3.39276e-05 | 0.00411858 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975597 | GAGGCAGTTAAGTTG[A/G]GTGAGTCCAACGCGC | 79836 |
rs755471423 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119015118 | ATAAATCAGGGAATA[C/T]TGTCTTTCTAGGATA | 79836 |
rs755518534 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | LONRF3 | GRCh38.p7 | X:119006834 | ACCTCATGATCCACC[C/T]GCCTCGGCCTCCCAA | 79836 |
rs755591733 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118984670 | CTTCAAGGAACTTAA[C/T]AATCTTGCATTTGTT | 79836 |
rs755608921 | snp | A/G | 2.74971e-05 | 0.0037078 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989654 | GAAACGGGGATGCCT[A/G]ATAAAGCCTCCAAGC | 79836 |
rs755647231 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118985671 | CATTTCTAGGATAAC[A/T]TAACGTGGTGTTGTT | 79836 |
rs755651841 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:119015558 | CCTGGCTCTGGGCCA[C/T]GATGAGTCAGGACTG | 79836 |
rs755679459 | snp | A/G | 4.17894e-05 | 0.00457088 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974796 | ATGGAGTCAGTACGG[A/G]TCGAACAGATGCTGA | 79836 |
rs755742276 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118983968 | AGAGGAGCACGGTTC[A/G]GGGAGAATTGCTTCA | 79836 |
rs755757301 | snp | C/G | 0.00105904 | 0.0229869 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973753 | CCGACCCCAGCAGGC[C/G]GGGTACATCCCTGCC | 79836 |
rs755823822 | snp | A/C/T | 4.62976e-05 | 0.00481114 | synonymous-codon, stop-gained, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017655 | CTGAATGGTATTCGA[A/C/T]GAGTCCTGGCCTTCA | 79836 |
rs755832476 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999828 | AACAAAACAAAACCC[C/T]CTGTGCCTGGAGTAG | 79836 |
rs755861911 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119010098 | TCTTATGAAAATCAA[A/T]TGAGTTTGTGCATAG | 79836 |
rs755901934 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979837 | GGGTGAGAAGAAAAA[C/T]GGCCTGGACACCTCT | 79836 |
rs755917717 | snp | C/G | 0.268079 | 0.249345 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973154 | CAGAGACCCGAGGGG[C/G]CCTGCCATAACCCAA | 79836 |
rs755939103 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118984850 | TTATTTACTAGATCA[G/T]TCCAGTTTCAGGGCT | 79836 |
rs755944086 | snp | G/T | 6.32371e-05 | 0.00562268 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974900 | GGGCCCCCACCCAAA[G/T]GTGGCTGCAGAGGGC | 79836 |
rs755949371 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:119000817 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 79836 |
rs755976197 | snp | A/C | 0.00581083 | 0.0535878 | intron-variant | LONRF3 | GRCh38.p7 | X:118986755 | GTTGATTCTGATGCC[A/C]GCTGAAGCGAGGACC | 79836 |
rs756019799 | in-del | -/A | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981007 | TGATGCCTATAATTC[-/A]AAACCACCTCCCACC | 79836 |
rs756028708 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118980508 | TGTGTACTGTGCAAT[C/G]AATGTCAGGTGAATC | 79836 |
rs756041747 | snp | G/T | 0.00105904 | 0.0229869 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018597 | CTTCAGCAATCTAAT[G/T]GTACGTGTATCTAAT | 79836 |
rs756086821 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119010249 | CTGGCTGTAAGAACA[C/G]CTCCCTTAGCAGAAA | 79836 |
rs756131060 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118996651 | ACACAGGCCAGGTGC[A/G]GTGGCTCATGCCTGT | 79836 |
rs756143412 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976615 | GGGAGGGTTGGGTGG[A/G]CTTTGCAGCTTCAAG | 79836 |
rs756155098 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118978009 | TTGTTGGTAATACTG[C/T]ACTCATAAACCAGGC | 79836 |
rs756240641 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994338 | AAGTAAAGGGGTGAA[A/G]AAAAGGCGTTTCATG | 79836 |
rs756256890 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118997255 | ACCAAAACAGCATGG[-/T]ACTCGTATAAAAATA | 79836 |
rs756288196 | in-del | -/TGTTG | | | intron-variant | LONRF3 | GRCh38.p7 | X:119006602 | TGTTTTGTTTTGTTT[-/TGTTG]AGACGGAGTCTCGCT | 79836 |
rs756442074 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012496 | AATCAAAATTTATTT[C/T]TCATGGTTCTGGAGG | 79836 |
rs756442979 | in-del | -/G | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118992039 | TTCACAAATGTGTCT[-/G]TTTTCCAAAAGAGCA | 79836 |
rs756457731 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119002787 | AACTTAAAAGCGCTT[C/G]TTCTTGTTTTTTTAT | 79836 |
rs756497121 | snp | A/G | 3.33673e-05 | 0.00408442 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975546 | AACCGACTGTACCGC[A/G]AGCGCCAGGTGGAGG | 79836 |
rs756500930 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118993060 | CTGACAGAGCCTACC[A/C]AAATGAGAAGGAACC | 79836 |
rs756609365 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118990960 | TCTCCCCAGTTCAAG[C/T]GATTCACGTGCCTCA | 79836 |
rs756650554 | snp | C/T | 6.53637e-05 | 0.00571643 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975441 | GGGCAGCAGCCGCCG[C/T]CGCCGCTGCGAGTCA | 79836 |
rs756669372 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988264 | ATTAAATGATTGAGA[A/T]TGCTAATACTGAACC | 79836 |
rs756711309 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119004659 | CCCAGGTGACTGGGG[G/T]AGGCAGGAAGGAGGG | 79836 |
rs756718589 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999458 | AAGCCCATGATGTGC[A/G]CTGTGGAGTAGACTT | 79836 |
rs756722628 | snp | G/T | 0.000297745 | 0.0121977 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017633 | AATGAGGTCCTTAAA[G/T]GACAGACTGAATGGT | 79836 |
rs756738560 | in-del | -/C | 0.000142278 | 0.00843319 | intron-variant | LONRF3 | GRCh38.p7 | X:119009114 | ATTGTCTAATTGCCT[-/C]CCCCCATGTAGTGCT | 79836 |
rs756859415 | snp | A/T | | | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989553 | AGGAGGAGAAGTGGG[A/T]TGCTACCTCTCCAAA | 79836 |
rs756881007 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118998331 | CCTGGATGAGATTGG[A/G]GACTATTTTAAGTGA | 79836 |
rs756881069 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119015686 | GGTAACGGGAAAACA[C/G]AGATGCTACAGTGTG | 79836 |
rs756936078 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118995316 | ATGACACAACCTATC[A/G]AAACCTCTGGGATAC | 79836 |
rs756971095 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119014955 | CATTAAATACTGTTA[A/G]TTGAGTTATACTAGA | 79836 |
rs756985755 | snp | C/T | 2.33451e-05 | 0.00341643 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014347 | GCCGGAGAAAGACGC[C/T]GATCCTCAGGTATAG | 79836 |
rs756988730 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119001322 | CACACATTTGTTGCC[A/G]CATCATAGAGTGAAG | 79836 |
rs757049675 | snp | C/T | 0.00528398 | 0.051128 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973972 | GCTGCCCAACTTCTG[C/T]GCCGGTGGGACCCGC | 79836 |
rs757067062 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999614 | AATCCTGAGGTGTAA[A/G]TTCTTTTGTTCCTCT | 79836 |
rs757083107 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118994549 | CTGAGATTACAGGCA[C/T]GTGCCACCATGCCCG | 79836 |
rs757104931 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981916 | CAATGGAGGAGGCAA[A/G]GGAGCAGGCCACTGG | 79836 |
rs757127581 | snp | A/G | 2.29993e-05 | 0.00339104 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989499 | CAGCTAAAGTGAAGG[A/G]GGATGGTCAGCAGCA | 79836 |
rs757146285 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:119011124 | GCTTAAAAAAAAAAA[A/G]AAAAAGAAAAAGAAA | 79836 |
rs757172048 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119010175 | TCTCTGCCGTGCACA[A/G]GTAATGTGAGAGGTG | 79836 |
rs757178086 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974413 | CTTCCGAAAAAGAAC[C/T]AGGTGGTGAGGAGGA | 79836 |
rs757217507 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119010193 | AATGTGAGAGGTGAA[C/G]GGGAGGGGCAGAGGC | 79836 |
rs757221467 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:119000829 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCACTGT | 79836 |
rs757272959 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118988679 | GTTCTCCATGTAAAT[A/C]TGCATAAACATGTTG | 79836 |
rs757294954 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118992323 | ACAGACTTGGAGCTG[C/T]TGGGGAGGGCACGGT | 79836 |
rs757378777 | snp | A/G | 2.28822e-05 | 0.0033824 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119009191 | AGCTAAATTCCTTCC[A/G]GAAGAACTGAAGGAA | 79836 |
rs757406924 | snp | C/T | 2.30306e-05 | 0.00339334 | synonymous-codon, nc-transcript-variant, downstream-variant-500B, utr-variant-3-prime, intron-variant | LONRF3 | GRCh38.p7 | X:119013174 | TGGCTACAACACAGC[C/T]GACATTGAATACATT | 79836 |
rs757451562 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118997347 | ACTGATCTTCAACAA[A/G]GCAAACAAAAACACA | 79836 |
rs757537866 | snp | A/T | 2.28217e-05 | 0.00337792 | missense, utr-variant-5-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118978423 | AGAATGCACTGCATG[A/T]TGCAGAAATAGCATG | 79836 |
rs757588936 | snp | A/G | 4.55877e-05 | 0.00477407 | missense, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982861 | TAGCCACCCTAGGCA[A/G]GGTGGAGGAGGCACT | 79836 |
rs757591421 | snp | G/T | 2.68276e-05 | 0.00366239 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975312 | TGTGGCCACACCTTT[G/T]GTAAACTGTGCCTGG | 79836 |
rs757667870 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119004650 | CATAGGCTCCCCAGG[A/T]GACTGGGGGAGGCAG | 79836 |
rs757710105 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976738 | AAGTGGCTGCTGAGC[C/T]GCCAGCCGGTGTTGC | 79836 |
rs757713267 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017990 | CCAAAAGTTTAAAGT[G/T]GTTTTGCTTTAATAT | 79836 |
rs757755872 | snp | C/G | 2.29938e-05 | 0.00339063 | intron-variant | LONRF3 | GRCh38.p7 | X:118990565 | CTATGTATGAGGTAC[C/G]TCCTGTGTACTATCA | 79836 |
rs757764282 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118984208 | GACTTTCCCAAGGTC[A/C]TGCAGCTGGTGATTG | 79836 |
rs757809061 | snp | C/T | 2.3175e-05 | 0.00340396 | intron-variant | LONRF3 | GRCh38.p7 | X:119006263 | TTCTTTCTTGTTTGG[C/T]TTAAATCAGTATTTC | 79836 |
rs757815453 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119002632 | TGTTCATTTTCTGTT[C/T]GCTTCCTTCTCTTTT | 79836 |
rs757840561 | snp | A/C | 9.24684e-05 | 0.00679895 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119009143 | CTTGGCATCAAGAAA[A/C]TACAGCAAAAATGTA | 79836 |
rs757870723 | in-del | -/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118993126 | ATTCTAACACCCCCC[-/T]CCCAAAAACCACACT | 79836 |
rs757877278 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987140 | TGTTTTGTGGGCAAA[C/T]GTGGGGAGTGAGCCC | 79836 |
rs757897639 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:119000169 | GTCCTTGGGGGAGAG[A/T]GTCTGAGAGTAAAGA | 79836 |
rs757903541 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119001779 | TGTGTGTTTTATTCA[C/T]CTGCTCACTAAATGT | 79836 |
rs757909008 | snp | A/C | 0.000147183 | 0.00857729 | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013235 | AAGAATCCCAAAGCC[A/C]GGCTATCCTTGTAAC | 79836 |
rs757921906 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988103 | TCCCTCCATTCATGC[C/T]CGGTGTTCTTCTCCT | 79836 |
rs758012861 | snp | A/G | 2.28566e-05 | 0.0033805 | missense, nc-transcript-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006221 | TGTCCATTGTGCAAA[A/G]ACGGTCTTTCACAGG | 79836 |
rs758041461 | snp | A/G | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012583 | TAACATAGTGGAAGG[A/G]CATAGCAGAAGGGCA | 79836 |
rs758066975 | snp | G/T | 2.08301e-05 | 0.00322717 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975128 | GGCGGAGAAAGTCCC[G/T]CAAGGCGAGGCGCTG | 79836 |
rs758072575 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118978933 | TAGCACTATATAAAC[A/G]TTCTCTTTCTTCCCT | 79836 |
rs758088009 | snp | C/T | 0.00039622 | 0.0140696 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975537 | CACGAGGGCAACCGA[C/T]TGTACCGCGAGCGCC | 79836 |
rs758098295 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119016593 | ACCTCGTGATCCACC[C/T]GCTGGCCTCCCAAAG | 79836 |
rs758137559 | snp | A/G | 3.07513e-05 | 0.00392106 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975269 | CCGGAAATGTCATGG[A/G]TTTCTATCAGACCCC | 79836 |
rs758213769 | snp | G/T | 6.85714e-05 | 0.005855 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989464 | AGCAGCCAGGGGAGA[G/T]GGCAGCAGTCTGATG | 79836 |
rs758322015 | snp | C/G | 2.27988e-05 | 0.00337622 | missense, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982900 | TTCTCTACTGTGTAT[C/G]CCTTGATGGAAAGAA | 79836 |
rs758335621 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974619 | GAGACAAGACAGTTA[C/T]TAGGCGGCGCGGGGC | 79836 |
rs758361427 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012163 | TGTCTATTTAAAGAA[C/G]CCTAGAATTAATATT | 79836 |
rs758363401 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119001604 | CCTAAATATAGAAAT[G/T]AATTGAGTATTGAAA | 79836 |
rs758372927 | snp | C/T | 0.003302 | 0.0404981 | intron-variant, missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118987052 | TGACTACTGAAGTTA[C/T]CAGCCATAATCTACC | 79836 |
rs758521302 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:119011130 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAGACCCT | 79836 |
rs758581545 | snp | C/T | 2.29679e-05 | 0.00338872 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118978355 | GACAGCTCCAAATGA[C/T]CACTTGCTTTATAGC | 79836 |
rs758589892 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118983239 | GAAAAACCAAAATCA[A/G]GTACATTAATATGGG | 79836 |
rs758681768 | snp | A/T | 2.35505e-05 | 0.00343143 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011989 | GTAAGTGAGGAGCCA[A/T]GCGAGCAAAGGGAGG | 79836 |
rs758719549 | snp | A/G | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972761 | TGAAATTTGGTCTTA[A/G]GATCAAAGCCACTCA | 79836 |
rs758734862 | snp | C/G | 3.45477e-05 | 0.00415604 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975611 | GGGTGAGTCCAACGC[C/G]CTGCCGGGCCGGGGC | 79836 |
rs758741014 | snp | C/G | 2.50925e-05 | 0.00354198 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119012918 | GCTGTAACCCAGGGA[C/G]AGGAAAATAGGCAGA | 79836 |
rs758841961 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119004792 | AATTGTACACTTTAC[A/G]TCTGTTCCATTTATT | 79836 |
rs758972780 | in-del | -/TATTTCTTTCTTGTTTGGTTTAAATCAG | 2.30258e-05 | 0.00339299 | intron-variant | LONRF3 | GRCh38.p7 | X:119006245 | TCACAGGTAAATCAA[-/TATTTCTTTCTTGTTTGGTTTAAATCAG]TATTTCTTTCTTGTT | 79836 |
rs759036988 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119010890 | AGGCAGAGGCCGGTG[A/G]ATTGCTTGAGGTCAG | 79836 |
rs759121345 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119000965 | AACAATACAAGGATG[C/T]AACTGGTGGGAAAAG | 79836 |
rs759129866 | in-del | -/GGCGCT | 4.1505e-05 | 0.0045553 | cds-indel, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975136 | AGTCCCGCAAGGCGA[-/GGCGCT]GGCGCTGGCGCCGGC | 79836 |
rs759137117 | snp | A/G | 0.00422943 | 0.0457911 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119019232 | GGGTGAAATATTTCA[A/G]TGTATGGGGAGAATA | 79836 |
rs759140458 | snp | A/G | 2.28035e-05 | 0.00337657 | missense, nc-transcript-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006200 | TGCCTAGATCACAAC[A/G]CAAAGTGTCCATTGT | 79836 |
rs759273942 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977090 | CTGCAGAAGAAAAAA[A/G]ACAGAAAAGACTAAA | 79836 |
rs759285676 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987983 | ATGGGTTCCAGGCCC[C/T]GGCTTTCCCGGCAGA | 79836 |
rs759317578 | in-del | -/TAT | | | intron-variant | LONRF3 | GRCh38.p7 | X:118990798 | GGGAAGGGAACAGTC[-/TAT]TCACAGGTCACAAAC | 79836 |
rs759325989 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118989036 | GACAGGATCTGCCGT[C/T]ACTGCCTGCCTTGGT | 79836 |
rs759435434 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118983963 | GCTTGAGAGGAGCAC[-/G]GTTCGGGGAGAATTG | 79836 |
rs759481042 | snp | C/G | 3.82044e-05 | 0.00437044 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975216 | ACGGGGGCCGCCGCG[C/G]CTGCGGCGGCCACCG | 79836 |
rs759581226 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119004239 | TTTTAATTAATTTGT[C/T]AAACAAATTAACTAC | 79836 |
rs759586281 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014122 | GAAGGCAGGATGGAT[A/G]CTCAAAGCGAATCAG | 79836 |
rs759588938 | snp | C/T | 3.60868e-05 | 0.0042476 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974991 | GAGAGCAAAGTCCTG[C/T]TCACGCAGGCAGACG | 79836 |
rs759695095 | snp | A/G | 3.29511e-05 | 0.00405887 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989636 | CAGATTGAATCCCAA[A/G]AAGAAACGGGGATGC | 79836 |
rs759716193 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118997647 | CTAACTAAACTAAAG[A/G]GCTTTTGCATGGCAA | 79836 |
rs759775463 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979455 | TGTGCCACCATGCCC[A/G]GCTAATTTTTTGTAT | 79836 |
rs759825130 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118983147 | GTACGATCAGTTTGG[A/G]CAGTTTCTACATTTT | 79836 |
rs759825271 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000428 | AGGACCATTCCAATC[C/T]CCAGGTCTCCCTTGC | 79836 |
rs759828670 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979145 | AGTTGGGACTACAGG[C/T]GCCCGCCACCACACC | 79836 |
rs759832006 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119008912 | TAAAAATTTTTTTCT[A/G]ATTATAAAGATAATC | 79836 |
rs759855874 | snp | A/G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999309 | GGGCTAAATGAGCAG[A/G/T]TTCCTTTCACTACTT | 79836 |
rs759950063 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118991530 | CTCTACTTTCTCAGA[G/T]CTCTGGAGAGGCAAA | 79836 |
rs759968116 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119007896 | AAGAAGAAAAATCTA[-/C]CCATATGCTCAGTAC | 79836 |
rs759970022 | in-del | -/GTA | 0.000529661 | 0.016265 | utr-variant-3-prime, nc-transcript-variant, cds-indel | LONRF3 | GRCh38.p7 | X:119018211 | TCTACATGTATGTTT[-/GTA]ACTATTTAAGCGTAC | 79836 |
rs760019830 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119009872 | CCTTCCGGGTTCAAG[A/C]GATTCTCCTGCCTCA | 79836 |
rs760063283 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118986669 | TCAAAATCCAGATTC[C/T]TGGGCCACACTCCAG | 79836 |
rs760068355 | snp | C/G | 0.00158814 | 0.0281345 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974316 | CCTGTTTGCTGGCCC[C/G]TTTGGAGGTGGGATG | 79836 |
rs760159423 | snp | A/G | 2.29263e-05 | 0.00338565 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime, intron-variant | LONRF3 | GRCh38.p7 | X:119013063 | ATATGGCTGCATCCT[A/G]GAGATCAGAAATGTT | 79836 |
rs760244834 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118995113 | AGCCTCACTAAATTT[A/G]AGAGAACTGAAATTA | 79836 |
rs760245129 | in-del | -/T | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:119002801 | CTTCTTGTTTTTTTA[-/T]TTTTTTTTTTATTTT | 79836 |
rs760246255 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118978526 | TATTGGCAGGAAGGG[A/C]TGCCTCCCTGGAGCA | 79836 |
rs760249614 | snp | C/T | 0.000529661 | 0.016265 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975115 | TGGTGCGCTGCCTGG[C/T]GGAGAAAGTCCCGCA | 79836 |
rs760257032 | snp | A/G | 2.36102e-05 | 0.00343578 | intron-variant | LONRF3 | GRCh38.p7 | X:118978309 | CTGCTTGCGCTGGGG[A/G]CCATTAATAAAGGTT | 79836 |
rs760369162 | snp | C/G | 0.000181274 | 0.00951863 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975198 | ACCGTGGCGGCGGAA[C/G]AGACGGGGGCCGCCG | 79836 |
rs760406560 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986703 | TGGGGGAGATGGGAG[C/T]ACAAAGTAGAGACCT | 79836 |
rs760422275 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119002312 | TTTAGCTTTACTACC[C/T]GAATATGTGTATCTA | 79836 |
rs760439785 | snp | A/G | | | stop-gained, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017563 | GCCCAGCCTGGTGCT[A/G]GTGGATGTTAGCAGT | 79836 |
rs760441398 | in-del | -/TTTT/TTTTT | | | intron-variant | LONRF3 | GRCh38.p7 | X:119016346 | TTCTTTCTTTCTTTC[-/TTTT/TTTTT]TTTCTTTTTTTTTTT | 79836 |
rs760451713 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118998555 | TCAGAAATCACCACT[A/G]AAGAACCTACTCATG | 79836 |
rs760464349 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003694 | GCTCTTCAGATGTAT[C/G]TTGGCTCTTGGCCCT | 79836 |
rs760551153 | in-del | -/CAT | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118997879 | TAAAGAAATGCTCAG[-/CAT]CACTAATGATCAGGA | 79836 |
rs760603505 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118990098 | GAGAAGCAGCAGCTG[C/T]GGCTTGCTATCTTTC | 79836 |
rs760604644 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987808 | AATGGATGTAATTTC[A/G]TATTCCTGCACTATG | 79836 |
rs760605920 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118994245 | AAAAGATACAGAACC[A/G]CAGAATGGATAAGAA | 79836 |
rs760684812 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:119006546 | GCTGGGATTACAGGC[A/G]CATGCCACCACGCTC | 79836 |
rs760727904 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118984931 | TCGAACTCACAGGCT[A/G]TGTTTCTTTTTAATG | 79836 |
rs760789941 | snp | C/T | 0.00025434 | 0.0112741 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974740 | CTTGCTTCGTGTCCC[C/T]GGTCCCTAGACGCCT | 79836 |
rs760911733 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979527 | ACTCCTGGCCTCAAG[C/T]AATCCACTTGCCTCA | 79836 |
rs760941217 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118997301 | GGAACAAAATAGAGA[A/C]CCCAGAAATAAACCC | 79836 |
rs760962876 | snp | A/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972700 | CAAGCCACCATCCAC[A/T]GCATTTGGACTAGTC | 79836 |
rs761048972 | snp | C/T | 0.000276956 | 0.0117644 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974834 | CGCTGAGGTCAGCAG[C/T]GACAACTTGGAGTCG | 79836 |
rs761088300 | snp | G/T | 0.000529661 | 0.016265 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119019004 | TTAGCCAGGCTTGGT[G/T]GTGTATGCCTGTAAT | 79836 |
rs761107016 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119009695 | TTCACGACCCTAGGC[A/G]GGTCATTTAACCTTT | 79836 |
rs761148357 | in-del | -/GC | 0.00528398 | 0.051128 | intron-variant | LONRF3 | GRCh38.p7 | X:118988162 | GACTGAAATGCAGGT[-/GC]GCCCAACTTTTCTTA | 79836 |
rs761162088 | snp | A/T | 0.0110639 | 0.0735497 | intron-variant | LONRF3 | GRCh38.p7 | X:119000806 | CTCTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC | 79836 |
rs761166184 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118998942 | TGGGATTACAGGCGT[A/G]AGCCACTATGCCTGG | 79836 |
rs761225159 | snp | A/G | 7.06256e-05 | 0.00594204 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017543 | GTTGCAGATGAACCC[A/G]AATGGCCCAGCCTGG | 79836 |
rs761226554 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979161 | GCCCGCCACCACACC[C/T]GGCTAATTTTTTGTA | 79836 |
rs761254881 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118996333 | AATCAGACAAGAGAA[A/T]GAAATAAAGGGCATC | 79836 |
rs761341712 | snp | C/T | 2.28475e-05 | 0.00337983 | missense, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982929 | AACAAGAGAGCAAGA[C/T]GTGAAGCCCAAAGAG | 79836 |
rs761358383 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118976275 | CCCGCGCGAGCGGGC[A/G]GGATTGTGTAACCGC | 79836 |
rs761381221 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118987322 | TCTTTCTATCACCCA[G/T]GCTGGAGGGCAGTGA | 79836 |
rs761393744 | snp | C/T | 2.28058e-05 | 0.00337674 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011839 | GAATGTGCCTATTTT[C/T]GTGTGTACTATGGCC | 79836 |
rs761402798 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119002912 | CAAGCGATTCTCCTG[C/T]CTCAGCCTCCCCAGT | 79836 |
rs761420555 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119008565 | TCAATATTTAGCTGT[C/T]TGTGTTTTTTTAAAC | 79836 |
rs761436957 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018289 | GTACCTAGGGGGAAA[A/T]AACAATACTAGAAGT | 79836 |
rs761437500 | snp | A/G | 4.15093e-05 | 0.00455554 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975520 | GAGCGTCGCAACTCC[A/G]GCACGAGGGCAACCG | 79836 |
rs761481889 | in-del | -/GT | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003983 | ATTGTGTGTGCACGT[-/GT]GTGTGTATTTATCTA | 79836 |
rs761518244 | snp | C/T | 4.72311e-05 | 0.00485935 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012833 | TATGTGCTCAATAAA[C/T]GGTAGCAGTTACACG | 79836 |
rs761528175 | snp | C/T | 0.000348592 | 0.0131975 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975375 | CTGTGCGGGGTCAAG[C/T]TCTCCGCCTTGATGG | 79836 |
rs761531814 | snp | C/T | 2.31524e-05 | 0.00340231 | intron-variant | LONRF3 | GRCh38.p7 | X:118990442 | CCGGGGTGGCTCCAG[C/T]GCTGACTTCTTGCTT | 79836 |
rs761552744 | snp | A/G | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973530 | TTCAGGAAGTGTGTA[A/G]GACACCGTCGAGGCC | 79836 |
rs761559358 | in-del | -/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119016350 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT | 79836 |
rs761560166 | snp | A/G | 2.49831e-05 | 0.00353425 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119012921 | GTAACCCAGGGACAG[A/G]AAAATAGGCAGAAGT | 79836 |
rs761618312 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119017344 | GCTGCAAGGGAAGCT[A/G]AGAAATGCAGTCTTT | 79836 |
rs761638225 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118981336 | CTAAAAATACAAAAC[A/T]TAGCCAGGCATGGTG | 79836 |
rs761678786 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118990325 | TGTCCCATTCTCAAC[A/G]GCTCAGGTGTCCACT | 79836 |
rs761717095 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002179 | ATACTTATGTAACCC[C/T]TCTCAGTTCAAGAAG | 79836 |
rs761728593 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119002226 | CCCAAGAAGCTACCC[A/G]TATGCCTCTTCCCAA | 79836 |
rs761750688 | snp | A/G | | | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976822 | GCATGCCGGGGAGGA[A/G]GCAGCAGGGCTGGGC | 79836 |
rs761763687 | in-del | -/A | 0.00633741 | 0.0559334 | intron-variant | LONRF3 | GRCh38.p7 | X:118999150 | GACCTTCTTTCTCTT[-/A]AAAAAAATTTTAGGT | 79836 |
rs761792690 | snp | A/G | 7.33532e-05 | 0.00605568 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017736 | TTCCCCACTGCCGTC[A/G]GGGGGAGTCTTCTTG | 79836 |
rs761823702 | snp | G/T | 0.000144201 | 0.00848999 | intron-variant | LONRF3 | GRCh38.p7 | X:119017500 | GATGTTCTTGGATGG[G/T]AATAGGATGACTCCA | 79836 |
rs761918851 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119007401 | GAGCTTTTGCAGACC[A/G]CAGCCCTCTAGGACT | 79836 |
rs761946874 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118986512 | AATTCCCCAAGTGAG[A/G]TTTCTCTCCTGACTT | 79836 |
rs762028442 | in-del | -/C | 0.0105399 | 0.0718252 | intron-variant | LONRF3 | GRCh38.p7 | X:119000863 | TCTCTCTTCCTCCCT[-/C]CCTCTCTCTCCCTAT | 79836 |
rs762106275 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118985236 | CTTGCACCTTGTGAT[G/T]CTGTGTGGCTGCCAC | 79836 |
rs762115831 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973656 | GCCACTGGGCTGTGC[C/T]GGGATTCGCGGACTT | 79836 |
rs762193147 | snp | A/G | 2.36055e-05 | 0.00343543 | intron-variant | LONRF3 | GRCh38.p7 | X:119009256 | TTTCTAAGTATGTAT[A/G]TGCATATTTCTGTTT | 79836 |
rs762214746 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118993636 | AAAACTTCCCCGGCC[G/T]TGTGAGAGACCTAGA | 79836 |
rs762255328 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:119010779 | GCTGGCTCTGTTTTG[G/T]TTCCCCAACGGGTTG | 79836 |
rs762270421 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118995567 | AATGTTCTTTGAAAA[A/G]ATAAGTAAAATTGAT | 79836 |
rs762277195 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972955 | TTCTCCTTCTCCTTC[C/T]TCTTCATTTTTTTTT | 79836 |
rs762306187 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118988225 | ATCACAGAACCCCCA[A/G]TGATTTCAATAATTA | 79836 |
rs762339411 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118994405 | TATATCAGACAAAAC[-/A]AAATTTTTTTTTTTT | 79836 |
rs762415710 | snp | A/T | 0.0251071 | 0.109193 | intron-variant | LONRF3 | GRCh38.p7 | X:119000810 | CTCTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC | 79836 |
rs762485368 | in-del | -/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118978829 | CCTCATCTGTTAAAT[-/G]GGGGATATTCAAAGC | 79836 |
rs762494789 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005893 | ATAGACTAGAATTGA[C/T]GTTACAAAATGATCT | 79836 |
rs762546449 | snp | A/G/T | 4.57721e-05 | 0.00478376 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011818 | TCTTTCTGACAGCCT[A/G/T]AATAAGAATGTGCCT | 79836 |
rs762551669 | snp | C/G | 2.32834e-05 | 0.00341192 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119009240 | GAGGAAATGGAAGAA[C/G]TTTCTAAGTATGTAT | 79836 |
rs762579239 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118989003 | GAATGGCAGTGAGGG[C/T]GAGAGGAACTATTGA | 79836 |
rs762681783 | snp | C/T | 4.78944e-05 | 0.00489336 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017722 | GAGGAGCTCCCACCT[C/T]CCCCACTGCCGTCGG | 79836 |
rs762744724 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119015629 | TTCCCCTTCACCTTC[C/T]GGGAAGCGTTCTCCC | 79836 |
rs762763140 | snp | A/T | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973390 | GGCAAGCCTAGTCCC[A/T]GCCTCCCTGCTTGGA | 79836 |
rs762767365 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118983059 | GTCCTGAGTGGGTGG[C/T]TCCCTGGGTTAAGGG | 79836 |
rs762779813 | snp | A/C | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118982220 | TGGTTAGCCCTCTGA[A/C]GGGCAGTCTGCTTTG | 79836 |
rs762815896 | in-del | -/CGCCGCGGCT | 0.0022652 | 0.0335778 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975209 | GGAAGAGACGGGGGC[-/CGCCGCGGCT]GCGGCGGCCACCGAG | 79836 |
rs762820627 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976479 | CCTGTGCCCTCGCCT[C/T]CAACCCCTTTAACCT | 79836 |
rs762826259 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119003007 | CAGGCTGGTCTTGAG[C/T]TCCTCACCCCAGATG | 79836 |
rs762880049 | snp | A/G | 4.34207e-05 | 0.00465923 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975509 | AGGCCCAGCGCGAGC[A/G]TCGCAACTCCGGCAC | 79836 |
rs762890991 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118984547 | ACCTGTCTCTCCAGT[C/T]TGCTTTTATAGAGAA | 79836 |
rs762920614 | snp | C/T | 2.28584e-05 | 0.00338064 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017608 | GCCGAGCTCAGCTCC[C/T]CTTCCTAGCAATGAG | 79836 |
rs762933282 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999331 | TCACTACTTCCCTCA[C/T]CCCCTCATGATAGAA | 79836 |
rs762967352 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999252 | AAGCAAGCCTCCCAT[C/G]CTGTCAGGAGTTGGT | 79836 |
rs763152626 | snp | A/G | 2.28055e-05 | 0.00337672 | missense, nc-transcript-variant, utr-variant-3-prime, intron-variant | LONRF3 | GRCh38.p7 | X:119013125 | ACAGCATAGGCAAGA[A/G]GCGCTTCAGGGTGCT | 79836 |
rs763215002 | snp | A/G | 0.000115017 | 0.00758258 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975168 | CCCCCGGACGAGGGT[A/G]GCACTGCAAGCGGCA | 79836 |
rs763218079 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119016433 | GCTCACTGCAAGCTC[C/T]GCCTCCCAGGTTCAC | 79836 |
rs763233861 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986009 | CAGGTTTTAGAAGCA[A/C]AGTCACCTGCTCTCC | 79836 |
rs763235089 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118978622 | TGGGCAAAGAGTGAC[C/T]CAGGTCTGCAAGGGA | 79836 |
rs763247038 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119011653 | TTTCAATATTTTTCT[A/C]TTAGCCATCAAAACT | 79836 |
rs763264293 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119007668 | TGAGCTTTACCATCA[A/C]CCCAGTATTTAAATT | 79836 |
rs763273163 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119006745 | AGGCGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 79836 |
rs763336518 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119010001 | GTCTTGAACTCCTGA[A/T]CTCAAGTGATCCTCC | 79836 |
rs763347940 | in-del | -/TT | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987445 | CCATGCCTGGCTAAG[-/TT]TTTTTTTTTTTTTTT | 79836 |
rs763388691 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002037 | TTTGGTTTGGCTGCT[C/T]TGATAATTAGATCAC | 79836 |
rs763422581 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119016850 | GACATGCAAAGGTCA[A/G]GGGGTCATGGGAATC | 79836 |
rs763444301 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118995083 | AAGATAGACCATATG[A/T]TAGACCATAAAATGA | 79836 |
rs763467505 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118986577 | AAAATCCCACTGCAG[A/C]TATTTCTGCGGAGTG | 79836 |
rs763491857 | snp | G/T | 2.35777e-05 | 0.00343341 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014222 | GTTCAGGGAGAGGAT[G/T]GTGCTGAGCTCATGG | 79836 |
rs763495957 | snp | A/G | 2.27946e-05 | 0.00337591 | missense, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982836 | GCACATTTCAGAAAA[A/G]CCCAAGCCTTAGCCA | 79836 |
rs763525270 | snp | C/T | 4.25913e-05 | 0.00461452 | stop-gained, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975513 | CCAGCGCGAGCGTCG[C/T]AACTCCGGCACGAGG | 79836 |
rs763561023 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118995172 | AATAAAACTGGAAAT[C/T]AACTGTAAAAGGAAC | 79836 |
rs763618820 | snp | C/T | 3.36214e-05 | 0.00409995 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975383 | GGTCAAGCTCTCCGC[C/T]TTGATGGTGGCCACT | 79836 |
rs763620277 | snp | C/T | 2.32032e-05 | 0.00340603 | intron-variant | LONRF3 | GRCh38.p7 | X:118982978 | GGTCCAGCTGCCTAC[C/T]GGACCCTCCCCTCTC | 79836 |
rs763680866 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119014794 | CTCCCTCATTGCTTT[G/T]GGAACTAGGGGATAG | 79836 |
rs763730589 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119016502 | ACAGAAGCCCGCCAC[C/T]GCGCCCGGCTAATTT | 79836 |
rs763793262 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002158 | TAACAAAATATTGTA[C/G]AGAAGATACTTATGT | 79836 |
rs763793672 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118981206 | AGTATATGGGTTGGC[C/T]GGGCATGGTGGCTTA | 79836 |
rs763811392 | snp | C/T | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973401 | TCCCTGCCTCCCTGC[C/T]TGGAGCAGTGCGACT | 79836 |
rs763819272 | in-del | -/A | 0.0328547 | 0.123887 | intron-variant | LONRF3 | GRCh38.p7 | X:119011112 | AGTGAGACTCCGCTT[-/A]AAAAAAAAAAAAAAA | 79836 |
rs763890169 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118989268 | GCCTTATGACGGCCC[C/T]CAAGTTGAGCTCTGT | 79836 |
rs763974147 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118980539 | TTGTATGTTCTTTCT[A/T]GAGAAGGTTTTCATG | 79836 |
rs763985049 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999506 | GACCAGGTCTTTGTT[G/T]TGCGTATCCTTCTTA | 79836 |
rs763997119 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118998603 | TACCCCAATAACTTA[C/T]GGAAAAATAAAATAA | 79836 |
rs764051453 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118997950 | CCTGTAAGAATGGCC[A/G]TAATAAAAAACTCAA | 79836 |
rs764051471 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000634 | GACATTTTGAGATAT[A/G]CAGTAAGAATGTTTG | 79836 |
rs764075207 | in-del | -/CAAAGTCCTGCTCACGCAGGCAGA | 4.18288e-05 | 0.00457303 | cds-indel, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975407 | GCCACTGGGCGGGCG[-/CAAAGTCCTGCTCACGCAGGCAGA]CGTGGAGCCCGGCGG | 79836 |
rs764171530 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119010040 | CCTCCCAAGGTGCTG[A/G]GATTACAGGCGTGAG | 79836 |
rs764198995 | snp | A/G | 2.28334e-05 | 0.00337878 | missense, nc-transcript-variant, downstream-variant-500B, utr-variant-3-prime, intron-variant | LONRF3 | GRCh38.p7 | X:119013149 | GGGTGCTCCATCAGA[A/G]CCAGCGGGATGGCTA | 79836 |
rs764211887 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119005479 | ATATATGTGTGTATA[C/T]GCATCAATATAGATC | 79836 |
rs764287207 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977959 | TAGGGGTCACATCTG[C/T]CCACCTCTCTCTCCT | 79836 |
rs764338762 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118983303 | ATGAGAGATCCAGGG[C/T]ATGGGGCTACCTGCT | 79836 |
rs764368368 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119015253 | GTCACAAAAGAAAAA[A/C]TCTCAATATGCATAT | 79836 |
rs764414240 | snp | A/G | 7.2197e-05 | 0.00600777 | intron-variant | LONRF3 | GRCh38.p7 | X:119009082 | TTTGCTGATTGCTAC[A/G]TATTACCTAATTGCA | 79836 |
rs764430995 | snp | A/G | 2.28733e-05 | 0.00338174 | missense, nc-transcript-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006224 | CCATTGTGCAAAGAC[A/G]GTCTTTCACAGGTAA | 79836 |
rs764449563 | in-del | -/C | 0.000142278 | 0.00843319 | intron-variant | LONRF3 | GRCh38.p7 | X:119009113 | ATTGTCTAATTGCCT[-/C]CCCCCCATGTAGTGC | 79836 |
rs764508119 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972792 | AGGTTAGAGCTGGAG[A/G]GAACCTTGGAGATTA | 79836 |
rs764532162 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:119000807 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 79836 |
rs764639891 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118977519 | TCCAAGTACTGCACA[C/T]ACCTTCAGAAAAAGG | 79836 |
rs764669960 | snp | A/C | 2.29282e-05 | 0.00338579 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119009169 | ATGTAATAATGGAGG[A/C]GCTCATAGCTAAATT | 79836 |
rs764677780 | snp | C/G | 0.000529661 | 0.016265 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018297 | GGGGAAATAACAATA[C/G]TAGAAGTGTGCAGTT | 79836 |
rs764687285 | in-del | -/T/TTT | 0.425459 | 0.178559 | intron-variant | LONRF3 | GRCh38.p7 | X:118994408 | ATCAGACAAAACAAA[-/T/TTT]TTTTTTTTTTTTTGA | 79836 |
rs764696607 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118987340 | TGGAGGGCAGTGATA[A/T]GATCATGGCTCACTG | 79836 |
rs764731175 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118995353 | GGCAGTGCTAAGAGG[A/T]TAGTTCATATCCCTG | 79836 |
rs764778186 | snp | A/C | 2.2849e-05 | 0.00337994 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118990495 | TGATCAGGGGGACAA[A/C]CCTGCTCTCAGTTTA | 79836 |
rs764855117 | snp | A/G | 6.87238e-05 | 0.0058615 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975231 | GCTGCGGCGGCCACC[A/G]AGGTGTGGGACGGCT | 79836 |
rs764863060 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119008001 | GTCACCTACTTTTTA[A/G]ACTGACTACCTCCTC | 79836 |
rs764876409 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002968 | CACAGTCTGCTAATT[C/T]TTATGGGATTTTGCC | 79836 |
rs764903101 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988014 | GGGTAAGTGGTCAGA[A/G]GTTGAGGATCAGAAG | 79836 |
rs764937392 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118982112 | AGCAGTTGGGCTTGG[A/G]CCCTGAGGAGCCATA | 79836 |
rs764946492 | snp | A/G | 2.28925e-05 | 0.00338315 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014308 | ATCCCTAAAGAATCG[A/G]ATACTCAATCACTTT | 79836 |
rs764953995 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118989124 | CTGGCATTTCCCCTT[C/T]TTACACCTGCCCAAG | 79836 |
rs764964176 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002220 | CCAGGACCCAAGAAG[C/T]TACCCATATGCCTCT | 79836 |
rs764983169 | snp | A/G | 0.000529661 | 0.016265 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017624 | CTTCCTAGCAATGAG[A/G]TCCTTAAAGGACAGA | 79836 |
rs765028825 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003997 | TGTGTGTGTATTTAT[C/G]TAGTAACTTTGTTAA | 79836 |
rs765120990 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974533 | TCTGGTTTTGTAACA[A/G]TTTCCCCGCCGCCGG | 79836 |
rs765142590 | snp | A/G | 0.000245459 | 0.0110756 | intron-variant, synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118987032 | AAAGGAAAACGTAGA[A/G]TCAATGACTACTGAA | 79836 |
rs765145528 | snp | A/G | 2.48531e-05 | 0.00352504 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119012925 | CCCAGGGACAGGAAA[A/G]TAGGCAGAAGTCCCT | 79836 |
rs765234808 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118981354 | GCCAGGCATGGTGAC[A/G]CATGCCTGTAGTCCC | 79836 |
rs765262000 | snp | C/G | 3.00062e-05 | 0.00387326 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975366 | CGCTGTGCGCTGTGC[C/G]GGGTCAAGCTCTCCG | 79836 |
rs765304640 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012082 | CATGAGGTTTAGCCA[A/G]CTGAAGAATATGAGC | 79836 |
rs765318132 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:119016289 | GGATTTATGTGGAAT[A/G]GGAAAGCTCTTTATT | 79836 |
rs765345286 | snp | C/T | 0.000529801 | 0.0162671 | intron-variant | LONRF3 | GRCh38.p7 | X:118978607 | CAGGGTAAAGATCCC[C/T]GGGCAAAGAGTGACT | 79836 |
rs765361438 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999250 | CAAAGCAAGCCTCCC[A/G]TGCTGTCAGGAGTTG | 79836 |
rs765383307 | snp | A/C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118978040 | TGCCGGACACTAGCC[A/C/G]TGTGTAGCCACATCT | 79836 |
rs765409110 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981353 | AGCCAGGCATGGTGA[C/T]GCATGCCTGTAGTCC | 79836 |
rs765413604 | snp | C/T | 4.3123e-05 | 0.00464323 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974869 | AGCGAGGGGCATCAG[C/T]GGCCCAAGTAGACAT | 79836 |
rs765472791 | snp | C/T | 2.76897e-05 | 0.00372076 | intron-variant, nc-transcript-variant, synonymous-codon | LONRF3 | GRCh38.p7 | X:119012887 | TCACACAGGCACTGC[C/T]TGTTGTGTAATTGAA | 79836 |
rs765476754 | snp | A/T | 2.2797e-05 | 0.00337609 | missense, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982826 | TTCCTTCCAGGCACA[A/T]TTCAGAAAAGCCCAA | 79836 |
rs765508267 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:119006692 | TCCCGGGTTCATGCC[A/G]TTCTCCTGCCTCAGC | 79836 |
rs765512220 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118998083 | CTTAAAGAACTAAAA[G/T]TAGAACTGCCATTTG | 79836 |
rs765545614 | in-del | -/AGCA | | | intron-variant | LONRF3 | GRCh38.p7 | X:119014917 | GCTATTGTCCTCACC[-/AGCA]AGGGCTGAACAGCTC | 79836 |
rs765599094 | snp | C/G | 0.0430067 | 0.140192 | intron-variant | LONRF3 | GRCh38.p7 | X:119000811 | TCTCTCTCTCTCTCT[C/G]TCTCTCTCTCTCTCT | 79836 |
rs765608902 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118983167 | TTCTACATTTTTGTA[A/G]GAGCCTGTGAGGAAT | 79836 |
rs765620021 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118993283 | CAAAAACTGGCACAA[G/T]AAGTGAAGGGAGAAA | 79836 |
rs765641395 | in-del | -/A | 2.34703e-05 | 0.00342558 | intron-variant | LONRF3 | GRCh38.p7 | X:119006083 | TTTATTTTTGGTCTT[-/A]ATTGCAGTTTTCTTC | 79836 |
rs765732980 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119006345 | CTGGACCCCCAGCCA[C/T]GGCACTGTGGTAGGG | 79836 |
rs765763674 | snp | C/T | 0.00158814 | 0.0281345 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973686 | TTCTCCTGAATAGCG[C/T]TCTCAGCTCGCGTCT | 79836 |
rs765778169 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119009907 | CCCGAGTAGCTGAGA[C/T]TACAGGCATGCACCA | 79836 |
rs765811050 | snp | A/G | 2.28035e-05 | 0.00337657 | missense, nc-transcript-variant, utr-variant-3-prime, intron-variant | LONRF3 | GRCh38.p7 | X:119013098 | TCTTTGCTGATGGCC[A/G]CTCAGTGGTTGACAG | 79836 |
rs765820177 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118977193 | AAACATCAAAGCCTG[C/T]TGCCACAGAGGAAGC | 79836 |
rs765826469 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | LONRF3 | GRCh38.p7 | X:119009856 | CTTACTGCAACCTCC[A/G]CCTTCCGGGTTCAAG | 79836 |
rs765834168 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119000887 | TCCCTATTTCTCCCT[-/C]TCCTTCTCCCCTCCC | 79836 |
rs765906852 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118993727 | TAGGCACATTGTCAT[C/T]AGATTATCCAAAGTT | 79836 |
rs765921512 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118980305 | GAGCTCTGGACAGCT[A/T]CCTGTAATCCAACAC | 79836 |
rs765923389 | in-del | -/T | 0.235898 | 0.249602 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972961 | TCTCCTTCTTCTTCA[-/T]TTTTTTTTTTTTTTC | 79836 |
rs765989791 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119001234 | GAGGAGAGAGGGAGG[A/G]AGGAAAATGTGCATA | 79836 |
rs766001451 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018445 | CCACTTTTTTTTTTC[A/G]GTTTGAACTAAACAA | 79836 |
rs766011906 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119002324 | ACCCGAATATGTGTA[C/T]CTAGGCGATGCAATC | 79836 |
rs766018980 | in-del | -/A | 0.487495 | 0.0780778 | intron-variant | LONRF3 | GRCh38.p7 | X:118996922 | GCTAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 79836 |
rs766056422 | snp | C/T | 0.00105904 | 0.0229869 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119019119 | CTCCAGCCTGGGCAA[C/T]GAGCAAACCTGCGTC | 79836 |
rs766072066 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976512 | CCAGCCCGGCGGGAG[G/T]CCGGCGCGGCAACTG | 79836 |
rs766151882 | snp | G/T | 0.000164541 | 0.00906883 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975204 | GCGGCGGAAGAGACG[G/T]GGGCCGCCGCGGCTG | 79836 |
rs766198744 | snp | C/T | 0.000200321 | 0.010006 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975050 | AGCCCTCGAGGTGTA[C/T]AGACAGCTCTCCGAG | 79836 |
rs766262867 | snp | A/G | 6.96233e-05 | 0.00589973 | missense, nc-transcript-variant, downstream-variant-500B, intron-variant | LONRF3 | GRCh38.p7 | X:119013187 | GCCGACATTGAATAC[A/G]TTGAAGACCAAAAGG | 79836 |
rs766308233 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118983072 | GGTTCCCTGGGTTAA[A/G]GGGACAAAAGGGAGA | 79836 |
rs766323161 | snp | C/G | 0.000124992 | 0.00790446 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974741 | TTGCTTCGTGTCCCC[C/G]GTCCCTAGACGCCTC | 79836 |
rs766342878 | snp | C/T | 0.000571082 | 0.0168883 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975608 | GTTGGGTGAGTCCAA[C/T]GCGCTGCCGGGCCGG | 79836 |
rs766356618 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013379 | CTATGGCAGTGAGGG[C/T]GCCTACTGTCCTGGC | 79836 |
rs766358542 | snp | C/T | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012052 | GGTACTCCCAGGAGA[C/T]AGGGAGGCCTAGCTC | 79836 |
rs766392721 | in-del | -/T | 4.69456e-05 | 0.00484465 | intron-variant | LONRF3 | GRCh38.p7 | X:118978322 | GGCCATTAATAAAGG[-/T]TTTTTCTTTCTTATT | 79836 |
rs766448100 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119007675 | TACCATCACCCCAGT[A/G]TTTAAATTAAGGGAA | 79836 |
rs766473606 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118980733 | AAGTCAGGGAGCTGC[C/T]TAGGAGTAAGAGGAC | 79836 |
rs766485761 | snp | G/T | 3.5548e-05 | 0.00421577 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974841 | GTCAGCAGCGACAAC[G/T]TGGAGTCGGCGGAGC | 79836 |
rs766491528 | in-del | -/TCACCA | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987488 | TGTAGAGACGGGGTT[-/TCACCA]TTTTTGCCTAGGCTG | 79836 |
rs766525508 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118998747 | CACTTTGTCACCCGG[A/G]CTGGAGTGCAGTGGT | 79836 |
rs766559660 | snp | A/G | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014111 | CCTTCCCATAGGAAG[A/G]CAGGATGGATGCTCA | 79836 |
rs766563145 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118999280 | GGTGTGGGTGGAGTG[C/G]GCTAGGGTGGGAGGG | 79836 |
rs766616247 | snp | A/G | 0.000480103 | 0.0154862 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012854 | CAGTTACACGAATAC[A/G]TTACGAATTTTTTTT | 79836 |
rs766746458 | snp | A/C | 2.361e-05 | 0.00343576 | intron-variant | LONRF3 | GRCh38.p7 | X:118978310 | TGCTTGCGCTGGGGG[A/C]CATTAATAAAGGTTT | 79836 |
rs766750738 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119008752 | ATGGAGACAATTTCT[A/G]TGAGCTTGTAAATAC | 79836 |
rs766760395 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118997565 | TGGCTTAGGCAAGGA[C/T]TTCATGACCGAGAAC | 79836 |
rs766779320 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:119015491 | CCCCCATGCAAAGGC[A/C]TCATGAGTTTTCAAG | 79836 |
rs766785991 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119006778 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 79836 |
rs766843165 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118978174 | CCAGAGTGGCTGGGG[A/G]TATAGAAGGCAGGAC | 79836 |
rs766875522 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:119017181 | AGAAAGGCTGATCCT[C/T]ACCACGTCCATGTTC | 79836 |
rs766890462 | snp | C/T | 2.27897e-05 | 0.00337555 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011881 | TCCTTGTCCCCTGCA[C/T]ATCTTTGAGCCTTGT | 79836 |
rs766898131 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118978626 | CAAAGAGTGACTCAG[A/G]TCTGCAAGGGAGCTG | 79836 |
rs766944308 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118991339 | GGATCCCAGCACTAA[C/T]CTCAGTTACATGGGC | 79836 |
rs766947625 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119016434 | CTCACTGCAAGCTCC[A/G]CCTCCCAGGTTCACG | 79836 |
rs766951861 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119007011 | TTACAGGCATGAGCC[A/T]CCACGCCCAGCCTAT | 79836 |
rs766972676 | snp | A/C | 0.00105904 | 0.0229869 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974257 | AGGTACCAGCCTCTC[A/C]TGGGAGGAGTGGGGG | 79836 |
rs767027892 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979763 | ATGGTTGTGCCATTT[A/C]AAGTCCTTAATATAG | 79836 |
rs767095760 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119009894 | CCTGCCTCAGCCACC[C/T]GAGTAGCTGAGATTA | 79836 |
rs767122227 | snp | A/G | 4.03714e-05 | 0.00449267 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975529 | AACTCCGGCACGAGG[A/G]CAACCGACTGTACCG | 79836 |
rs767138018 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119017435 | CAATCTGCCACATGG[A/G]GTTGTTCTACCTGGG | 79836 |
rs767187909 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119015842 | AGTTTGCTCCAGTCA[A/T]TGCTGCATCCCCAGT | 79836 |
rs767200889 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118980448 | TGAAAATAATGGATT[A/G]TCAGAACTTTTTTGG | 79836 |
rs767202719 | snp | A/G | 2.45435e-05 | 0.00350302 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017740 | CCACTGCCGTCGGGG[A/G]GAGTCTTCTTGTAAA | 79836 |
rs767228641 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119010937 | TGCCCAGCATGGTGA[A/G]ACCCCATCTCTAATA | 79836 |
rs767228656 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119000815 | TCTCTCTCTCTCTCT[C/G]TCTCTCTCTCTCTCT | 79836 |
rs767229302 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118989262 | AATAATGCCTTATGA[C/T]GGCCCCCAAGTTGAG | 79836 |
rs767257372 | snp | C/G | 5.08195e-05 | 0.00504055 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974886 | GCCCAAGTAGACATG[C/G]GCCCCCACCCAAAGG | 79836 |
rs767299207 | snp | A/G | 4.62652e-05 | 0.00480942 | intron-variant | LONRF3 | GRCh38.p7 | X:118990443 | CGGGGTGGCTCCAGC[A/G]CTGACTTCTTGCTTT | 79836 |
rs767337529 | snp | A/C | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973777 | CCCTGCCGCGCCCAT[A/C]CGGCCAGTGGCTCCA | 79836 |
rs767356243 | snp | A/G | 0.000189807 | 0.00974 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975022 | CCTTGGCGTCCCGGG[A/G]GCGAATCCGTGAAGC | 79836 |
rs767388555 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118997808 | CCCATCAAAATATGG[A/G]CTAAGGACATGAATA | 79836 |
rs767404245 | snp | C/G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118984803 | ATGAGGCCATGGCGG[C/G/T]GATTCAGAACATCAA | 79836 |
rs767576286 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118983213 | ACTCAGGGTCTGGAT[C/T]GTCAGTGGGAGAAAA | 79836 |
rs767593971 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119000039 | GGCTATTTCAAACAC[A/G]TGCTTCAGCTTGAAT | 79836 |
rs767610350 | snp | C/T | 2.29753e-05 | 0.00338927 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014265 | GTGTCTATCAGCAAG[C/T]ATCATTGTGGTTTCA | 79836 |
rs767662893 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014151 | AGGTGTCAAAAGTGA[C/T]TCTGGGAATGATGGA | 79836 |
rs767675853 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013615 | TGTATTTTAAAGTAC[A/G]TAACCTGGCTAAGAG | 79836 |
rs767799135 | snp | C/T | 2.37758e-05 | 0.0034478 | intron-variant | LONRF3 | GRCh38.p7 | X:119009261 | AAGTATGTATATGCA[C/T]ATTTCTGTTTTGTTT | 79836 |
rs767886101 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972683 | TCCCCTCAACCCCGG[G/T]TCAAGCCACCATCCA | 79836 |
rs767923157 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979157 | AGGCGCCCGCCACCA[C/T]ACCTGGCTAATTTTT | 79836 |
rs767924409 | snp | A/G | 3.44566e-05 | 0.00415056 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975404 | GGTGGCCACTGGGCG[A/G]GCGCGTGGAGCCCGG | 79836 |
rs767973572 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119008993 | ATTATGATGGTAACA[A/G]CTGCTAATTTGTGGG | 79836 |
rs768071296 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118980390 | CACTTTATATCAGTT[C/T]AGGTCAGGTTTTGCC | 79836 |
rs768088088 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119004303 | CAAAAAGTTGAATAC[A/G]TGAAAAGTCTCTCTC | 79836 |
rs768146523 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999690 | TTTGGAGGAGGTCTC[-/A]AAATTTGGTCCAAGA | 79836 |
rs768188837 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013842 | GACATACTCCTGTGT[C/T]TTTTCCAGCAAGTAA | 79836 |
rs768307270 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118991441 | TAGCTTTTGTTTTGT[G/T]TTGTGCCATGAATAT | 79836 |
rs768323298 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118976210 | GGAATTAGGTCAGGA[C/G]AGCACTGGTTGCATA | 79836 |
rs768339006 | in-del | -/ACACACA | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986094 | CACACACACACACAC[-/ACACACA]CAATCCTTGCTAGTA | 79836 |
rs768384375 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118991139 | CTGGGATTACAGGCC[A/G]CTGCACCCAGTCTGA | 79836 |
rs768413474 | snp | A/T | 7.82381e-05 | 0.00625403 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974806 | TACGGATCGAACAGA[A/T]GCTGAGCTTGCCCGC | 79836 |
rs768431699 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118982031 | GGCAGCCCTCTCCCC[C/T]GCTACTCTTTTTTCT | 79836 |
rs768468882 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118999145 | ATGTGGACCTTCTTT[C/T]TCTTAAAAAAAATTT | 79836 |
rs768472701 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119008504 | AAATCATGACTTTTA[A/G]TCTCAGTGATACCTA | 79836 |
rs768531568 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018856 | AAGGAACCAGATGGC[C/T]GGGCACGGTGGCTCA | 79836 |
rs768586420 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118993001 | GGGAACACCCCGTGG[A/G]GCAAAAGAATCTGAA | 79836 |
rs768589486 | in-del | -/TTTC/TTTCTTTC | 0.444032 | 0.157644 | intron-variant | LONRF3 | GRCh38.p7 | X:119016330 | TAGGGGCAGAATATA[-/TTTC/TTTCTTTC]TTTCTTTCTTTCTTT | 79836 |
rs768632270 | snp | A/G | 0.000137268 | 0.00828344 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975647 | CTCGGTGGCTACATG[A/G]GGGAGCGGGAGAACA | 79836 |
rs768636173 | snp | C/G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119007337 | CCTCACAGAACTTCA[C/G/T]TGTGATCCTTGTCCA | 79836 |
rs768667756 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118986472 | CATTTGTAGACTTCT[A/G]CCCACTGAGGTATTA | 79836 |
rs768744365 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119016214 | AAAGCTCGTTTTAGG[C/T]TTAGAAGGAAATAAG | 79836 |
rs768753376 | snp | C/G | 0.000584397 | 0.0170838 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975175 | ACGAGGGTAGCACTG[C/G]AAGCGGCACCGTGGC | 79836 |
rs768819191 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986017 | AGAAGCAAAGTCACC[A/T]GCTCTCCTTGTGTTA | 79836 |
rs768838739 | snp | A/G | 2.33448e-05 | 0.00341641 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014234 | GATTGTGCTGAGCTC[A/G]TGGGATTACATAACT | 79836 |
rs768856276 | in-del | -/A | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118994835 | AAGTCCCAAATTTAT[-/A]AAAACAATTACGAAT | 79836 |
rs768856539 | in-del | -/ACACACACAC | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986052 | TTTCAGTATATGGAA[-/ACACACACAC]ACACACACACACACA | 79836 |
rs768878465 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119010758 | TAAGACAAGGATCCC[A/G]GAAGAGCTGGCTCTG | 79836 |
rs768892104 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987561 | GGCCTTCCAAAGTGC[C/T]AGGATACATTTTTTT | 79836 |
rs768920774 | snp | C/T | 2.35555e-05 | 0.00343179 | intron-variant | LONRF3 | GRCh38.p7 | X:119009119 | CTAATTGCCTCCCCC[C/T]ATGTAGTGCTTGGCA | 79836 |
rs768943431 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973526 | CGCCTTCAGGAAGTG[G/T]GTAGGACACCGTCGA | 79836 |
rs768945061 | in-del | -/G | 0.00523404 | 0.0508884 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974127 | GGGTTGTGTGTGTGT[-/G]GGGGGGGCTTCACGG | 79836 |
rs768975885 | snp | A/C | 2.73778e-05 | 0.00369975 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975336 | TGCCTGGAACGTGGG[A/C]GGGCCGCCGACCGGC | 79836 |
rs768981976 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003118 | AGTCAAAATTATCAA[C/T]CTTTTCATTTATAGA | 79836 |
rs769013837 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118994336 | TGAAGTAAAGGGGTG[A/T]AAAAAAGGCGTTTCA | 79836 |
rs769019329 | in-del | -/TCTCTCTCTCTCTCTCTCTCTCTCTC | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000784 | CTCTCATTCTCTCTC[-/TCTCTCTCTCTCTCTCTCTCTCTCTC]TCTCTCTCTCTCTCT | 79836 |
rs769050845 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118980846 | GCAGTGAAGCATTTT[A/G]GATGAAATGGGAAAA | 79836 |
rs769091222 | snp | C/T | 2.33822e-05 | 0.00341915 | intron-variant | LONRF3 | GRCh38.p7 | X:118989393 | ATTCTGATATGTGGC[C/T]CTTTCTTCATCCAGG | 79836 |
rs769112406 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118997159 | AAAAGAGCCTGCATA[A/G]CCAAAGCAAGACTAA | 79836 |
rs769158454 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118996802 | TGGCATGCACCTGTA[G/T]TCCCAGCTACTCGGG | 79836 |
rs769159248 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118988941 | CTGTGCCAAAGCCCT[A/G]CCAAAAGTCCTTTTG | 79836 |
rs769161849 | in-del | -/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118997587 | ACCGAGAACCGAAAA[-/G]CAAATGCAATAAAAA | 79836 |
rs769313155 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119004892 | TGGTTGAGAATTATT[A/G]TTGTAATAGAAAAGG | 79836 |
rs769325975 | snp | C/T | 0.0001423 | 0.00843384 | intron-variant | LONRF3 | GRCh38.p7 | X:118989369 | GAGGACAATATTAGT[C/T]CTAAGAAGATTCTGA | 79836 |
rs769360659 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118983755 | GAGCCTTACGGTTTC[G/T]GTCCCAGTGTGGTTT | 79836 |
rs769371292 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118976968 | GGGGAGGAGGAGGAG[A/G]AATGAGGACTGAAGG | 79836 |
rs769447337 | in-del | -/G | 2.50526e-05 | 0.00353916 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119012920 | TGTAACCCAGGGACA[-/G]GAAAATAGGCAGAAG | 79836 |
rs769500262 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013891 | AATGAAAAGGGCAAA[A/G]GCATGGACCAGCATA | 79836 |
rs769504665 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118982164 | GTATGTGGTGAGGGA[G/T]CAGAAGTGATCCAGG | 79836 |
rs769522270 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118993275 | AGGAAATCCAAAAAC[C/T]GGCACAAGAAGTGAA | 79836 |
rs769530643 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005878 | AATTCCCCAGAAGAG[A/G]TAGACTAGAATTGAT | 79836 |
rs769533597 | in-del | -/GGCGGCGGAAGAGACGGGGGCCGCCGCGGCTGC | 0.000501379 | 0.0158252 | cds-indel, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975188 | TGCAAGCGGCACCGT[lengthTooLong]GGCGGCCACCGAGGT | 79836 |
rs769602723 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976391 | CTGCCCTGTGACTCA[C/T]TGTCACCGCTTCCTA | 79836 |
rs769630031 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118992612 | GAAGACAAAGGGCAT[A/C]TAATCTTGGGAGTTC | 79836 |
rs769662347 | snp | A/G | 5.30926e-05 | 0.00515204 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975485 | CGGCCTCCTCGGCAA[A/G]TTGTTTCCAGGCCCA | 79836 |
rs769714641 | snp | C/T | 3.52566e-05 | 0.00419846 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975632 | GGGCCGGGGCTGGGG[C/T]TCGGTGGCTACATGA | 79836 |
rs769724419 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119008224 | GAATTAAATATTCCA[A/G]TCATTTTCACTGCAG | 79836 |
rs769737503 | snp | A/G | 0.00211696 | 0.0324653 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017906 | TTCTTGACATGCTGC[A/G]TAACTACATAAACAG | 79836 |
rs769739038 | snp | C/T | 2.2945e-05 | 0.00338703 | intron-variant | LONRF3 | GRCh38.p7 | X:119011812 | ATTTTCTCTTTCTGA[C/T]AGCCTTAATAAGAAT | 79836 |
rs769740214 | in-del | -/CAAAA | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999804 | TTCTAAGTGAGACTT[-/CAAAA]CAAAACAAAACAAAA | 79836 |
rs769745609 | snp | C/T | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973251 | ATTCTAAAGTTTGAC[C/T]TCCCCAAGGTCATCT | 79836 |
rs769770290 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119016546 | TAGAGATGGGGTTTC[A/G]TCGTGTTAGCCAGGA | 79836 |
rs769802998 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118978982 | CTTTCTCTCTCTCTC[C/T]CTTTCTGTTTTCTTT | 79836 |
rs769811988 | snp | A/G | 2.34321e-05 | 0.00342279 | intron-variant | LONRF3 | GRCh38.p7 | X:119006090 | TTTGGTCTTATTGCA[A/G]TTTTCTTCCATTTTG | 79836 |
rs769815680 | snp | A/G | 3.63471e-05 | 0.00426289 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974996 | CAAAGTCCTGCTCAC[A/G]CAGGCAGACGCCTTG | 79836 |
rs770025329 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119001987 | ATATAAGGCATTCAG[A/G]TTCACAGGACTAAGT | 79836 |
rs770083905 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974152 | TCACGGATACCCCTC[C/T]CAACCTGCTTCCTTT | 79836 |
rs770089277 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118994978 | TTAAATTATGCCTTG[G/T]AACAAATGGACTTAA | 79836 |
rs770109753 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118984415 | CTTATCTTTGGGGAC[A/G]GAGCGTGCAAAGGCC | 79836 |
rs770113449 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018457 | TTCAGTTTGAACTAA[A/G]CAATATAAAATACTT | 79836 |
rs770205515 | snp | C/T | 2.30455e-05 | 0.00339444 | intron-variant | LONRF3 | GRCh38.p7 | X:118982958 | AGTGAGTTGAAATGA[C/T]ATCAGGTCCAGCTGC | 79836 |
rs770240573 | snp | C/T | 2.39249e-05 | 0.00345859 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014200 | ACTTCCACTTTGATA[C/T]TTTCAGGTTCAGGGA | 79836 |
rs770243962 | in-del | -/A | | | intron-variant | LONRF3 | GRCh38.p7 | X:118997201 | AAATCTGGAGGCATC[-/A]AACTATCTGATTTCA | 79836 |
rs770258126 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119011514 | TAGCTATCATCCACA[A/G]TATTAAGATACTAGA | 79836 |
rs770264749 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:119010868 | CGTGTAATCCTAGTA[G/T]TTTGGGAGGCAGAGG | 79836 |
rs770269729 | snp | C/G | 5.43242e-05 | 0.00521144 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975331 | AACTGTGCCTGGAAC[C/G]TGGGCGGGCCGCCGA | 79836 |
rs770291809 | snp | A/T | 7.23031e-05 | 0.00601218 | intron-variant | LONRF3 | GRCh38.p7 | X:119014378 | AAAAATGTCTATTTT[A/T]AAACGGGTTGTCCCA | 79836 |
rs770339714 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118989117 | CCTATCCCTGGCATT[G/T]CCCCTTTTTACACCT | 79836 |
rs770466634 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118980087 | TGAGGGTCAAAAGTG[A/G]ACGTGGCCAAGAGGA | 79836 |
rs770485321 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118995049 | CACATTCTATTCAAC[A/G]GTGCATGAAACTTTC | 79836 |
rs770509516 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977720 | TGACATCTAGTAATT[C/T]AGAGTTTTTGGTGAG | 79836 |
rs770632105 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003739 | AAAGTTTAGAAATCA[A/G]CTTGTCAAGTTCTAC | 79836 |
rs770635603 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118996854 | GTGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC | 79836 |
rs770638125 | snp | G/T | 5.55532e-05 | 0.00527006 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975342 | GAACGTGGGCGGGCC[G/T]CCGACCGGCGCTGTG | 79836 |
rs770679542 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118978552 | GAGCATAGGGGCACT[A/G]GAGCTCAAGCAGAAC | 79836 |
rs770721971 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119000572 | TACCTTAGCCATTGG[G/T]GGCCACCTCTGGGGC | 79836 |
rs770740828 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119015094 | TTCACTAAGCTTTGC[C/T]TGCCTGGAATAAATC | 79836 |
rs770797827 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977085 | GTGTGCTGCAGAAGA[A/G]AAAAGACAGAAAAGA | 79836 |
rs770855563 | snp | C/T | 2.32393e-05 | 0.00340868 | intron-variant | LONRF3 | GRCh38.p7 | X:119011775 | TTTTTGTGTTCTGTC[C/T]GATTGCTTTGAGATC | 79836 |
rs770856254 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118993334 | TTAAAGAAAAAACAA[G/T]AAAAAATTCAGGAAA | 79836 |
rs770926061 | snp | A/C | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972900 | TTCCAATGTGTCCCT[A/C]GTGCTTTCCTGACTA | 79836 |
rs770950553 | snp | C/T | 2.56657e-05 | 0.00358221 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989625 | GGAAACATTGCCAGA[C/T]TGAATCCCAAGAAGA | 79836 |
rs770957264 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005476 | TGTATATATGTGTGT[A/G]TATGCATCAATATAG | 79836 |
rs771003739 | snp | A/T | 2.32032e-05 | 0.00340603 | intron-variant | LONRF3 | GRCh38.p7 | X:118990426 | AGTACTATCTATGAA[A/T]CCGGGGTGGCTCCAG | 79836 |
rs771019302 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973315 | AGGTCTTCAGGCCCC[C/T]GGGGCGGCAACCTGG | 79836 |
rs771074382 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118979439 | GCTGGGATCACAGGC[A/G]TGTGCCACCATGCCC | 79836 |
rs771115655 | snp | A/G | 4.76815e-05 | 0.00488247 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017712 | GATTGCCGAAGAGGA[A/G]CTCCCACCTTCCCCA | 79836 |
rs771147133 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118976060 | GAGAGGAACTTCGCG[C/T]GCTCCTCGCACTTGC | 79836 |
rs771194037 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118996084 | GTATGCTGATTTTGC[C/T]GAGAGTGTTAATCAT | 79836 |
rs771197354 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972657 | ATGGACAATCTTCCA[C/T]TGATTTCCCATCCCC | 79836 |
rs771215009 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118987972 | ACACAAGAGAGATGG[A/G]TTCCAGGCCCTGGCT | 79836 |
rs771242137 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999026 | GCTCAGATATTTCCT[C/T]GCCCTTTATGAGCAC | 79836 |
rs771247494 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119008941 | TCAATTGCATGTGTG[-/T]TTTTTTAAATGAAAC | 79836 |
rs771249138 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118987237 | GAACCTCTTAAAGAT[A/G]CAACTGTGAATTTCA | 79836 |
rs771323905 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119015396 | CCTCTTCCTCTTGCA[C/T]TCTGAGGTTCTAAGA | 79836 |
rs771329148 | snp | C/T | 0.000138985 | 0.00833507 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974967 | CAGTCTCCGGGGACC[C/T]CAACGCCGGAGAGCA | 79836 |
rs771343895 | snp | C/T | 2.33304e-05 | 0.00341536 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119013021 | ATCTAGTCTCTCGAC[C/T]CCATTCTCAATAAAC | 79836 |
rs771376398 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118996694 | TTGGGAGGCCAAGGC[A/G]GGCAGATCACGAGGT | 79836 |
rs771387922 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012766 | AATTAAATTTCAAAA[C/T]GGGTTGTAGAGGAGG | 79836 |
rs771404741 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118984277 | AGCCTGGCCTCTTAG[A/C]TGCTCTGCCATCCTG | 79836 |
rs771432042 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000303 | AACAAGTTAGAGTAT[A/G]AATTTGTATACACGG | 79836 |
rs771442091 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118985542 | CCTGGGCCCTGGGGT[A/G]GATAAGTGTCTTAAT | 79836 |
rs771443044 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002734 | ACCTTCTCCTACTCT[A/G]GCTTGCCTTTTTGCC | 79836 |
rs771487079 | snp | C/T | 0.00359439 | 0.0422407 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975013 | AGGCAGACGCCTTGG[C/T]GTCCCGGGGGCGAAT | 79836 |
rs771517568 | snp | C/G | 0.00119674 | 0.0244324 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975149 | CGAGGCGCTGGCGCC[C/G]GCGCCCCCGGACGAG | 79836 |
rs771548934 | in-del | -/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118997919 | AATCAAAACCACATT[-/G]AGATACCACCTTACT | 79836 |
rs771577749 | snp | G/T | 4.64727e-05 | 0.00482019 | intron-variant | LONRF3 | GRCh38.p7 | X:118978494 | AAGAGGTGGGAAGGG[G/T]TTGTACTGTAGACAG | 79836 |
rs771588840 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994697 | TGAGTCACTGCACCC[A/G]GCCCAAAACAAACTC | 79836 |
rs771650273 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118981883 | TCACTTCATTCACTA[A/T]GTTAGGCTTAGTACT | 79836 |
rs771684189 | snp | A/C | 5.09758e-05 | 0.0050483 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012839 | CTCAATAAATGGTAG[A/C]AGTTACACGAATACA | 79836 |
rs771684591 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119010973 | ACAAAAATTAGCCAG[C/G]CATGGTGGCATGCAC | 79836 |
rs771693667 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118991284 | ACCTGTGTGTCACAA[C/T]TGCATTACATTCTTA | 79836 |
rs771774621 | snp | C/T | 2.28284e-05 | 0.00337842 | synonymous-codon, nc-transcript-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006151 | AGTCACAACACCTTG[C/T]GGGCATACTTTTTGC | 79836 |
rs771818027 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118993087 | AACCAGAAAACCAAC[C/T]GTGGTAATATGACAA | 79836 |
rs771820657 | snp | A/G | | | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976900 | GTGGAGGAGGGGTGT[A/G]GGCCGGAGTCTCCAC | 79836 |
rs771843814 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118985863 | AGAGAATAAATCAAA[C/T]TGGAGTTTGGTGTTC | 79836 |
rs771845454 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977917 | ACCTGGAAAAGTAAC[C/T]TGGATTTGTCTTCTT | 79836 |
rs771855093 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999046 | TTTATGAGCACATAT[G/T]CTTCTCATATCGATC | 79836 |
rs771855146 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118990019 | TCTAGGAATGCAGGA[C/T]GAGGAAAGTGAGGTC | 79836 |
rs771881860 | in-del | -/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118998904 | ACCTCAGGTGATCCA[-/C]CCGCCTTGGCCTTCC | 79836 |
rs772004887 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118984849 | TTTATTTACTAGATC[A/T]TTCCAGTTTCAGGGC | 79836 |
rs772013928 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119000839 | TCTCTCTCTCTCTCT[A/C]ACTGTCACTCTCTCT | 79836 |
rs772106064 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119015935 | TACCAGCTTAAATAT[A/C]TTTGTTGGTGATCCT | 79836 |
rs772111801 | in-del | -/TG | 0.00422943 | 0.0457911 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974116 | GGGCTGGGACTGGGT[-/TG]TGTGTGTGTGTGGGG | 79836 |
rs772156448 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987707 | GAAGAGGGCCTAACA[A/G]TCCCTCCTTTCGAGC | 79836 |
rs772156533 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005232 | CTCCTCTTGGTGAGT[C/G]CAAGCCCCACTCCTC | 79836 |
rs772186030 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118993509 | AAATATGAACAAAGC[C/T]TCCAAGAAGTCTGGG | 79836 |
rs772327033 | snp | A/G | 0.000121481 | 0.00779267 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975469 | TCAACGTGGTGCTCA[A/G]CGGCCTCCTCGGCAA | 79836 |
rs772351526 | in-del | -/TT | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119000686 | TGGCCCAGTGACCTC[-/TT]TGTCAATTCTAACAA | 79836 |
rs772370342 | snp | C/G | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013866 | CAAGTAATGAGAAAA[C/G]AGATGTAAAAATGAA | 79836 |
rs772423576 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118997536 | GATAACATTGGAAAA[A/T]CCCTTCTAGACATTG | 79836 |
rs772432048 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118982685 | TTAGAACAGTTGCCC[A/G]CATTTTAGGGCTGTA | 79836 |
rs772456972 | snp | A/G | 2.53014e-05 | 0.00355669 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989614 | GGAAAAGAAAAGGAA[A/G]CATTGCCAGATTGAA | 79836 |
rs772479367 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119010325 | CTCCTCCCTCCATCC[A/G]CAGTAGAATCCTAAC | 79836 |
rs772515700 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118998907 | TCAGGTGATCCACCC[A/G]CCTTGGCCTTCCAAG | 79836 |
rs772544484 | snp | A/G | 0.00105904 | 0.0229869 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018910 | GAGGCCGAGGCAGGC[A/G]GATCACTTGAGGTCA | 79836 |
rs772567073 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119015269 | TCTCAATATGCATAT[C/T]CTGACCAAAAGTCTG | 79836 |
rs772578689 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118993187 | GAAATCCTTGATTTA[C/T]CTGAATAAGAATTGA | 79836 |
rs772590261 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119003918 | AGTTGCAAATGTTAT[C/G]TTTAAGATGATGACA | 79836 |
rs772597903 | snp | A/C | 3.41151e-05 | 0.00412994 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974932 | CCGCACCTCTACCGA[A/C]GCGGGAGCCAGAGCA | 79836 |
rs772604543 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999930 | GAAAGAACTTTGGAT[C/T]TTGAGGTTCTGAAAA | 79836 |
rs772605479 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975984 | TCTCTGTTCCTCTGA[-/CT]CTCCTTCTCCCGCTG | 79836 |
rs772655864 | snp | A/G | 2.34107e-05 | 0.00342123 | intron-variant | LONRF3 | GRCh38.p7 | X:118978509 | GTTGTACTGTAGACA[A/G]GTATTGGCAGGAAGG | 79836 |
rs772672874 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976450 | CCCCCCTTGCCCGCC[C/T]CGCCAACCCGTAGCC | 79836 |
rs772743836 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118988169 | ATGCAGGTGCGCCCA[A/C]CTTTTCTTAAAAAAT | 79836 |
rs772773482 | snp | A/G | 0.00211696 | 0.0324653 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018225 | TGTAACTATTTAAGC[A/G]TACATTGCTGAAAAG | 79836 |
rs772853619 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118983763 | CGGTTTCTGTCCCAG[C/T]GTGGTTTGGCAGAGC | 79836 |
rs772886995 | snp | A/G | 4.72205e-05 | 0.00485881 | intron-variant | LONRF3 | GRCh38.p7 | X:118978308 | CCTGCTTGCGCTGGG[A/G]GCCATTAATAAAGGT | 79836 |
rs772903322 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118983053 | TTTGGGGTCCTGAGT[C/G]GGTGGTTCCCTGGGT | 79836 |
rs772910181 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119004122 | TCCTCTCCAGTTCTC[A/T]TTTTTTTTCTTGCCT | 79836 |
rs772944759 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994726 | TCTAAAGCAACAGCA[C/G]TTAAAAGAGACAAAG | 79836 |
rs772949041 | snp | C/T | 7.01738e-05 | 0.005923 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119013017 | AAGGATCTAGTCTCT[C/T]GACTCCATTCTCAAT | 79836 |
rs772973447 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118977024 | GACCCTTCTAGCTCC[C/T]GTCTGTGCACAAGCA | 79836 |
rs772995861 | in-del | -/TTTTG | | | intron-variant | LONRF3 | GRCh38.p7 | X:119006573 | CTCGGCTAATTTTTG[-/TTTTG]TTTTGTTTTGTTTTG | 79836 |
rs773044078 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119004910 | GTAATAGAAAAGGCA[C/T]ATGACTGAAGTGGAA | 79836 |
rs773049030 | snp | C/T | 6.84088e-05 | 0.00584805 | synonymous-codon, nc-transcript-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006166 | CGGGCATACTTTTTG[C/T]TTAAAATGCCTAGAA | 79836 |
rs773102372 | snp | C/G | 1.86465e-05 | 0.00305334 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975185 | CACTGCAAGCGGCAC[C/G]GTGGCGGCGGAAGAG | 79836 |
rs773113708 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119007531 | TGTTTTCCCTCCCTC[A/G]GGGACTTATCTGCCA | 79836 |
rs773116812 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118999824 | ACAAAACAAAACAAA[A/C]CCCTCTGTGCCTGGA | 79836 |
rs773150169 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013893 | TGAAAAGGGCAAAGG[C/G]ATGGACCAGCATAAC | 79836 |
rs773159745 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003548 | AAATCAAGAATCCAC[A/G]TCTGGATCTGTTTCT | 79836 |
rs773160878 | in-del | -/GCC | 0.00232419 | 0.0340102 | cds-indel, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975434 | GCGGGCTGGGCAGCA[-/GCC]GCCGCCGCCGCTGCG | 79836 |
rs773246927 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118995920 | TCTACCAGACATTCA[A/G]AGAAGAATTGGTGCC | 79836 |
rs773264129 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988644 | TTGACCTATGGACTA[C/T]GGGTTTAGATTAGAG | 79836 |
rs773342014 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119008793 | AAATGGAAAGGGAAG[A/G]ATTCCCCCCACCCTA | 79836 |
rs773428199 | snp | A/G | 0.000142633 | 0.0084437 | intron-variant | LONRF3 | GRCh38.p7 | X:119017531 | TTGTGTTTCTCTGTT[A/G]CAGATGAACCCGAAT | 79836 |
rs773508565 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118986542 | TTACCTCTCTGTCTC[C/T]TTCCTCCTAGATGAG | 79836 |
rs773519153 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118997296 | CCAATGGAACAAAAT[A/G]GAGAACCCAGAAATA | 79836 |
rs773521252 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118980987 | GAGGTTAAGAGAAGA[C/T]GAACTGATGCCTATA | 79836 |
rs773579937 | snp | C/T | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013878 | AAACAGATGTAAAAA[C/T]GAAAAGGGCAAAGGC | 79836 |
rs773618387 | snp | A/T | 4.62856e-05 | 0.00481047 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012842 | AATAAATGGTAGCAG[A/T]TACACGAATACATTA | 79836 |
rs773631271 | snp | C/T | 0.0029668 | 0.0384005 | intron-variant | LONRF3 | GRCh38.p7 | X:118987117 | TCGCTCGTGACGCTT[C/T]GTTTGGCTGTTTTGT | 79836 |
rs773635261 | in-del | -/G | 0.000529801 | 0.0162671 | intron-variant | LONRF3 | GRCh38.p7 | X:118978608 | AGGGTAAAGATCCCT[-/G]GGCAAAGAGTGACTC | 79836 |
rs773705086 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119008536 | ATGGTATATTAGAAA[G/T]GCAAATAGACAAATC | 79836 |
rs773708223 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119011648 | TTGCATTTCAATATT[C/T]TTCTATTAGCCATCA | 79836 |
rs773752117 | in-del | -/C | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118989934 | CAAGCACAGTATCAA[-/C]TAATGACATCCCATA | 79836 |
rs773763519 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974208 | GAGGGAGAGTCTTAG[A/G]CGTCCCGGAAGACCC | 79836 |
rs773793483 | snp | A/G | 3.42243e-05 | 0.00413654 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974829 | TTGCCCGCTGAGGTC[A/G]GCAGCGACAACTTGG | 79836 |
rs773834878 | snp | C/G | 2.56575e-05 | 0.00358163 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012025 | TAATGAGGGATTTCT[C/G]TTTTACTTTGGGGTA | 79836 |
rs773861315 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:119010885 | TTGGGAGGCAGAGGC[C/T]GGTGGATTGCTTGAG | 79836 |
rs773895785 | snp | C/T | 4.16441e-05 | 0.00456293 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975519 | CGAGCGTCGCAACTC[C/T]GGCACGAGGGCAACC | 79836 |
rs773993661 | snp | C/T | 2.28357e-05 | 0.00337896 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011827 | CAGCCTTAATAAGAA[C/T]GTGCCTATTTTCGTG | 79836 |
rs774011222 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118977739 | GTTTTTGGTGAGAGC[C/T]GGCCTCACCTTATTC | 79836 |
rs774078491 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119009784 | CTCATGGACTTCTTT[G/T]TTTGAGATTGAGTCT | 79836 |
rs774084259 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118993024 | AATCTGAACAACAGC[C/T]TTTAGCCCTAGACCT | 79836 |
rs774092078 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119017318 | AGAACTTTGTCTCAT[A/G]GCCTCACCTAGCTGC | 79836 |
rs774170149 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118991217 | AATGTCTTGAGACAG[A/G]ACATGTACTCTCCAT | 79836 |
rs774184455 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118998460 | TGGGGACTTGGGGGG[A/G]AAAGTGGGAAGGGGG | 79836 |
rs774250056 | snp | G/T | 4.62824e-05 | 0.00481031 | intron-variant | LONRF3 | GRCh38.p7 | X:118990441 | ACCGGGGTGGCTCCA[G/T]CGCTGACTTCTTGCT | 79836 |
rs774286199 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000902 | CTCCTTCTCCCCTCC[C/G]TCCTCTCCTCCTCCT | 79836 |
rs774297168 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119005130 | CGAGGGAGCCGTGCA[G/T]CTGGCAGCCTCTGAC | 79836 |
rs774394403 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003280 | CTTGCCTCAGCACCC[C/G]CGCCTCAAGTAGCTG | 79836 |
rs774395040 | in-del | -/G | 0.00143823 | 0.0267778 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017735 | TTCCCCACTGCCGTC[-/G]GGGGGGAGTCTTCTT | 79836 |
rs774434698 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119008947 | GCATGTGTGTTTTTT[C/T]AAATGAAACTAACAT | 79836 |
rs774441719 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118992777 | GTCCATTGCACCCAC[C/T]ACCACCTCCACCAGA | 79836 |
rs774461957 | snp | A/G | 0.0001369 | 0.00827232 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975338 | CCTGGAACGTGGGCG[A/G]GCCGCCGACCGGCGC | 79836 |
rs774468503 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986241 | AACCTCCTTGCGCCT[A/G]GTACTTAAACTTAAC | 79836 |
rs774482614 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999891 | TCTCACTGCTTGATG[A/G]TGATAAGAAACCTAC | 79836 |
rs774536724 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972670 | CATTGATTTCCCATC[C/T]CCTCAACCCCGGTTC | 79836 |
rs774537424 | snp | C/T | 2.40541e-05 | 0.00346792 | intron-variant | LONRF3 | GRCh38.p7 | X:119017493 | GCAGACTGATGTTCT[C/T]GGATGGGAATAGGAT | 79836 |
rs774618247 | snp | C/G | 0.000121462 | 0.00779208 | intron-variant | LONRF3 | GRCh38.p7 | X:118986887 | ACCTGGGCACCTGTA[C/G]AAACTTAAGTAGTGA | 79836 |
rs774799401 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118987263 | TTTCAGGCATGGTCC[C/T]AGAGTTTATTCATTA | 79836 |
rs774873597 | in-del | -/C | 0.00158814 | 0.0281345 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018087 | GTATAATTTCACTGA[-/C]TTGAGGTCTCATTCC | 79836 |
rs774926868 | snp | A/G | 3.76053e-05 | 0.00433604 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974816 | ACAGATGCTGAGCTT[A/G]CCCGCTGAGGTCAGC | 79836 |
rs774944546 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118997164 | AGCCTGCATAGCCAA[A/G]GCAAGACTAAGCAAA | 79836 |
rs774982880 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002105 | AAATTGTGAAATACA[C/T]ACAGTGGAAAAGTGC | 79836 |
rs774983133 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118976103 | GGGCTGTAGCCAGCA[A/G]GAGATGTCCGGTCGG | 79836 |
rs775027026 | snp | C/T | 2.3337e-05 | 0.00341584 | intron-variant | LONRF3 | GRCh38.p7 | X:118989395 | TCTGATATGTGGCCC[C/T]TTCTTCATCCAGGAC | 79836 |
rs775041755 | in-del | -/ACACACAC | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986054 | TCAGTATATGGAAAC[-/ACACACAC]ACACACACACACACA | 79836 |
rs775215363 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119008314 | ACTCAGGCGCTCCCC[C/G]TGCTGGGACTGTAGG | 79836 |
rs775223434 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118990043 | TGAGGTCAGGCCTCA[A/C]CCTGCTCATTCCCAG | 79836 |
rs775250542 | in-del | -/TC | 2.3417e-05 | 0.00342169 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119013012 | TCATCAAGGATCTAG[-/TC]TCTCGACTCCATTCT | 79836 |
rs775265450 | in-del | -/GGGGG | 0.00169221 | 0.0290386 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975203 | GGCGGCGGAAGAGAC[-/GGGGG]CCGCCGCGGCTGCGG | 79836 |
rs775303670 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005886 | AGAAGAGATAGACTA[A/G]AATTGATGTTACAAA | 79836 |
rs775305269 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119015576 | TGAGTCAGGACTGCA[A/G]CATATACCTCTGAGC | 79836 |
rs775339786 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119006520 | GTTCTCCTGCCTCAG[A/C]CTCCCAAGTAGCTGG | 79836 |
rs775346498 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118981200 | AGGTAGAGTATATGG[G/T]TTGGCCGGGCATGGT | 79836 |
rs775509484 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118980126 | AAGCTATAAAGCTTC[C/T]TGGATGTAGTGCTCT | 79836 |
rs775599901 | snp | C/T | 0.000203863 | 0.0100941 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975491 | CCTCGGCAAGTTGTT[C/T]CCAGGCCCAGCGCGA | 79836 |
rs775603332 | snp | C/G | 2.29342e-05 | 0.00338623 | missense, nc-transcript-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006134 | AGATTATTCTATGAG[C/G]CAGTCACAACACCTT | 79836 |
rs775613691 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118993557 | AACCTAATAATAATC[A/G]GTGTACCTGTGGAAG | 79836 |
rs775615378 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000520 | TCCTCAATCCTTAGT[A/G]GTTGCAAATTCTCCT | 79836 |
rs775707202 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119016583 | CGATCTCCTGACCTC[A/G]TGATCCACCCGCTGG | 79836 |
rs775717542 | snp | C/T | 0.00791544 | 0.0624105 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972696 | GGTTCAAGCCACCAT[C/T]CACAGCATTTGGACT | 79836 |
rs775719073 | snp | C/T | 0.000176243 | 0.00938564 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975001 | TCCTGCTCACGCAGG[C/T]AGACGCCTTGGCGTC | 79836 |
rs775794355 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118985902 | TTTGTTGATCAATTA[A/G]TACCCTAACTATGTA | 79836 |
rs775798531 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119009924 | ACAGGCATGCACCAC[C/T]ATGCCCAGCGAATTT | 79836 |
rs775876922 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018933 | TGAGGTCAGGAGTTC[A/G]AGAGCAGCCTAACTA | 79836 |
rs775885985 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118984450 | GAGGCAGGTCTCAGA[C/G]CCAAGGAGGAATGGT | 79836 |
rs775904470 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119000842 | CTCTCTCTCTCTCAC[G/T]GTCACTCTCTCTTCC | 79836 |
rs775949266 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119009040 | ATGTGGGTCATTTGA[C/G]TTGTTCACTGATTAC | 79836 |
rs775991633 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118978634 | GACTCAGGTCTGCAA[A/G]GGAGCTGGATTCTTC | 79836 |
rs776001120 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119011533 | TAAGATACTAGAGAA[C/T]TTCTTCAGCCAAATT | 79836 |
rs776017504 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118988153 | TCATAAAAGGACTGA[A/G]ATGCAGGTGCGCCCA | 79836 |
rs776071284 | in-del | -/T | 0.497968 | 0.0318103 | intron-variant | LONRF3 | GRCh38.p7 | X:118991864 | AGTAAATGTTAACTA[-/T]TTTTTTTTTCCTTGT | 79836 |
rs776088478 | snp | A/G | 2.28035e-05 | 0.00337657 | missense, nc-transcript-variant, utr-variant-3-prime, intron-variant | LONRF3 | GRCh38.p7 | X:119013115 | TCAGTGGTTGACAGC[A/G]TAGGCAAGAGGCGCT | 79836 |
rs776141582 | snp | A/G | 2.36821e-05 | 0.003441 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014215 | CTTTCAGGTTCAGGG[A/G]GAGGATTGTGCTGAG | 79836 |
rs776157121 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:119002836 | TGGAGTCTCACTCTG[C/T]TGCCCAGGCTGGAGT | 79836 |
rs776260759 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118976211 | GAATTAGGTCAGGAG[A/C]GCACTGGTTGCATAA | 79836 |
rs776266152 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005560 | CTATGAAAATTATCT[A/G]TATAAAAGGCAGTTA | 79836 |
rs776293889 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118992513 | CACAGCAGCTGCAGC[A/G]AGACCTGCCCAAGGA | 79836 |
rs776314397 | snp | A/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012861 | ACGAATACATTACGA[A/T]TTTTTTTTCTTCACA | 79836 |
rs776334276 | snp | A/G | 2.28019e-05 | 0.00337645 | missense, nc-transcript-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006198 | GATGCCTAGATCACA[A/G]CGCAAAGTGTCCATT | 79836 |
rs776369224 | snp | C/T | 2.28938e-05 | 0.00338325 | synonymous-codon, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982937 | AGCAAGATGTGAAGC[C/T]CAAAGAGTGAGTTGA | 79836 |
rs776398886 | in-del | -/T | 8.44202e-05 | 0.00649638 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974762 | AGACGCCTCGTCTCC[-/T]TCCCGTGTCCCTCTT | 79836 |
rs776462444 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987878 | GAGAAGAGGAAAGAG[A/G]TGTTGGAAAGAAAGT | 79836 |
rs776482880 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999148 | TGGACCTTCTTTCTC[A/T]TAAAAAAAATTTTAG | 79836 |
rs776494214 | snp | A/T | 0.00066133 | 0.0181722 | intron-variant | LONRF3 | GRCh38.p7 | X:118982776 | TAGAGCAGTAGTGTT[A/T]ATAGGCTGAATAAAA | 79836 |
rs776496199 | snp | A/G | 0.0002145 | 0.0103539 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975165 | GCGCCCCCGGACGAG[A/G]GTAGCACTGCAAGCG | 79836 |
rs776516019 | snp | C/T | 3.57353e-05 | 0.00422687 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974842 | TCAGCAGCGACAACT[C/T]GGAGTCGGCGGAGCG | 79836 |
rs776544305 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119007357 | ATCCTTGTCCAACCC[-/A]TCAGGAGCCACTGTA | 79836 |
rs776551651 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003817 | AGTTGTTTAATTTCT[C/T]TCAATGAGGTGTTTG | 79836 |
rs776597808 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977972 | TGCCCACCTCTCTCT[C/T]CTTCCTACCTGGCCT | 79836 |
rs776627084 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118998628 | AAATAAATTAAAAAC[A/G]GAAATTAAGAAGATT | 79836 |
rs776635693 | snp | C/T | 6.12614e-05 | 0.00553416 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975470 | CAACGTGGTGCTCAG[C/T]GGCCTCCTCGGCAAG | 79836 |
rs776650396 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:119016258 | AAATATGTGCCAGGG[A/G]AGCTGCTTTGGGGAA | 79836 |
rs776677311 | snp | C/T | 4.64371e-05 | 0.00481834 | intron-variant | LONRF3 | GRCh38.p7 | X:118990428 | TACTATCTATGAAAC[C/T]GGGGTGGCTCCAGCG | 79836 |
rs776685060 | snp | C/T | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973170 | CCTGCCATAACCCAA[C/T]TCTGAAACATGACTT | 79836 |
rs776741431 | snp | A/G | 2.29845e-05 | 0.00338995 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119009158 | ATACAGCAAAAATGT[A/G]ATAATGGAGGAGCTC | 79836 |
rs776793517 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974128 | GGGTTGTGTGTGTGT[G/T]GGGGGGCTTCACGGA | 79836 |
rs776795382 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118986488 | CCCACTGAGGTATTA[C/T]GAACTTCAAATTCCC | 79836 |
rs776811692 | snp | A/C | 3.55183e-05 | 0.00421401 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974973 | CCGGGGACCTCAACG[A/C]CGGAGAGCAAAGTCC | 79836 |
rs776849836 | snp | C/T | 4.59237e-05 | 0.00479163 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime, intron-variant | LONRF3 | GRCh38.p7 | X:119013060 | AGAATATGGCTGCAT[C/T]CTAGAGATCAGAAAT | 79836 |
rs776871614 | snp | A/G | 2.61677e-05 | 0.00361707 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989635 | CCAGATTGAATCCCA[A/G]GAAGAAACGGGGATG | 79836 |
rs776947971 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118988995 | ACGGCCGTGAATGGC[A/G]GTGAGGGCGAGAGGA | 79836 |
rs776957521 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118980855 | CATTTTGGATGAAAT[-/G]GGAAAAGTGACTTCT | 79836 |
rs776970590 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119009808 | TGAGTCTCACTCTGT[C/T]ACCCAAGCTGGAGTG | 79836 |
rs777011932 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999104 | TGTTGGATGACTGAA[A/G]ACGAGTAACACAGCC | 79836 |
rs777087710 | snp | A/T | 0.0430067 | 0.140192 | intron-variant | LONRF3 | GRCh38.p7 | X:119000808 | CTCTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC | 79836 |
rs777096244 | snp | A/G | 2.41987e-05 | 0.00347833 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014169 | TGGGAATGATGGAGA[A/G]GGTACAGAATGTTTC | 79836 |
rs777118368 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118984375 | ACTTTCCAGTTCCAG[C/G]ATGAACAAAGGCAGT | 79836 |
rs777142536 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:119000855 | ACTGTCACTCTCTCT[C/T]CCTCCCTCCCTCTCT | 79836 |
rs777212522 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119008830 | GGACAAGAACATGAT[C/T]TTGATTTCAGTGTTT | 79836 |
rs777246047 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119011040 | AATTGCTTGAACCCG[A/G]GAGGCGGAGGTTGCA | 79836 |
rs777268667 | snp | A/G | 2.93423e-05 | 0.00383018 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975275 | ATGTCATGGGTTTCT[A/G]TCAGACCCCGTGTCC | 79836 |
rs777302500 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118985714 | TTATGGTGCACTCTC[C/T]ACTACTGTGTAGAAC | 79836 |
rs777331856 | snp | C/T | 2.28001e-05 | 0.00337632 | synonymous-codon, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982904 | CTACTGTGTATCCCT[C/T]GATGGAAAGAACAAG | 79836 |
rs777336022 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118994137 | GCAAAAACAAAAACC[A/G]AAGTACACACGCAAC | 79836 |
rs777348458 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118984673 | CAAGGAACTTAACAA[G/T]CTTGCATTTGTTAAC | 79836 |
rs777422567 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118979963 | ATTTGAGCCTGTGCT[C/T]TACTACTTGCAAACC | 79836 |
rs777437247 | snp | A/G | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012616 | AGAGAGAGAGAGAAA[A/G]AAGGGGGTCAAACTT | 79836 |
rs777461280 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119006017 | AAAGAACTCCTCCCC[C/T]ACCCTAAAATATTCT | 79836 |
rs777474606 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973838 | GCCTACCGCCTGCCC[C/T]AGCGCTAGTTCTGGC | 79836 |
rs777561547 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119014956 | ATTAAATACTGTTAG[C/T]TGAGTTATACTAGAC | 79836 |
rs777564224 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118993293 | CACAAGAAGTGAAGG[C/G]AGAAATATTCATGGA | 79836 |
rs777564277 | in-del | -/CTCTCTCTCTCTCACTGTCACTCTCTCTTCCTCCC | 0.0105399 | 0.0718252 | intron-variant | LONRF3 | GRCh38.p7 | X:119000827 | TCTCTCTCTCTCTCT[lengthTooLong]TCCCTCTCTCTCCCT | 79836 |
rs777616399 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973195 | TGACTTAATCCCAAG[G/T]AAGATCAGCTCTAAC | 79836 |
rs777617220 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005349 | GTACAGAACAAATTT[A/G]TAAAAGGATTCCCAC | 79836 |
rs777618505 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118998030 | CTGCTGGTGGGAATG[C/T]AAACTAGTACAACCA | 79836 |
rs777620810 | in-del | -/C | 0.00528398 | 0.051128 | intron-variant | LONRF3 | GRCh38.p7 | X:119015616 | ATCAAGCTTAATGTT[-/C]CCCTTCACCTTCCGG | 79836 |
rs777666659 | snp | C/T | 0.000321595 | 0.0126765 | intron-variant | LONRF3 | GRCh38.p7 | X:118987103 | TCAACTCACCCAGCT[C/T]GCTCGTGACGCTTCG | 79836 |
rs777697814 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119007351 | AGTGTGATCCTTGTC[C/T]AACCCATCAGGAGCC | 79836 |
rs777722271 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018619 | GTATCTAATTTTTCC[C/T]CAGTGCAGTTAGGAA | 79836 |
rs777808152 | in-del | -/TTTT | | | intron-variant | LONRF3 | GRCh38.p7 | X:119014976 | TATACTAGACAGTAG[-/TTTT]TTTGTTAGGTTCTAC | 79836 |
rs777809086 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979419 | CCACCTTAGCCTCCC[A/G]AGTAGCTGGGATCAC | 79836 |
rs777857577 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017991 | CAAAAGTTTAAAGTG[A/G]TTTTGCTTTAATATT | 79836 |
rs777864118 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118979869 | AGGATGCCAGGATGC[A/G]AAGTGTCACTTTCTG | 79836 |
rs777918568 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118992115 | AGGCTGCTGTTCGTT[G/T]TGCTGGCGGGTCCTG | 79836 |
rs777966027 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118982633 | CTGGGCAAGTTAACG[-/T]TTTTTGGGTTTCAGT | 79836 |
rs777987868 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976621 | GTTGGGTGGGCTTTG[C/T]AGCTTCAAGGGTAAC | 79836 |
rs778001704 | snp | C/T | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972798 | GAGCTGGAGGGAACC[C/T]TGGAGATTAAGAGAA | 79836 |
rs778008416 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118990372 | AGGTGGTGGTGAGAG[C/T]GGCAAACTGAAAAAC | 79836 |
rs778134653 | snp | A/G | 4.56767e-05 | 0.00477873 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118990526 | CCACTTGCATCTTTC[A/G]ACGCATCTGACCTTG | 79836 |
rs778163408 | snp | A/C | 8.41007e-05 | 0.00648408 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975616 | AGTCCAACGCGCTGC[A/C]GGGCCGGGGCTGGGG | 79836 |
rs778178765 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000025 | TGGATGTTGACAGAG[C/G]CTATTTCAAACACAT | 79836 |
rs778305304 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012618 | AGAGAGAGAGAAAGA[A/G]GGGGGTCAAACTTGC | 79836 |
rs778418021 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119016508 | GCCCGCCACCGCGCC[A/C/T]GGCTAATTTTTTGTA | 79836 |
rs778468244 | in-del | -/C | 2.33081e-05 | 0.00341372 | intron-variant | LONRF3 | GRCh38.p7 | X:119006278 | TTTAAATCAGTATTT[-/C]TTTCTTGTTTTGTTT | 79836 |
rs778475284 | snp | A/T | | | intron-variant, missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118987007 | AGCTGTTGGCACCTC[A/T]CCCTAGATTAAAGGA | 79836 |
rs778491594 | snp | A/G | 2.35441e-05 | 0.00343096 | intron-variant | LONRF3 | GRCh38.p7 | X:118978316 | CGCTGGGGGCCATTA[A/G]TAAAGGTTTTTCTTT | 79836 |
rs778508090 | snp | A/C | 2.27938e-05 | 0.00337586 | synonymous-codon, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982878 | GTGGAGGAGGCACTA[A/C]GGGAGTTTCTCTACT | 79836 |
rs778527615 | snp | C/T | 1.9823e-05 | 0.00314819 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975108 | GAGCAGCTGGTGCGC[C/T]GCCTGGCGGAGAAAG | 79836 |
rs778657179 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:119000831 | TCTCTCTCTCTCTCT[C/G]TCTCTCTCACTGTCA | 79836 |
rs778689103 | snp | A/C | 8.41786e-05 | 0.00648708 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974918 | GGCTGCAGAGGGCCC[A/C]GCACCTCTACCGACG | 79836 |
rs778697211 | in-del | -/GGCACT | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:119006345 | TGGACCCCCAGCCAC[-/GGCACT]GGCACTGTGGTAGGG | 79836 |
rs778745730 | snp | A/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:118994564 | CGTGCCACCATGCCC[A/G]GCTAATTTTTGTATT | 79836 |
rs778751787 | snp | C/T | | | | | GRCh38.p7 | X:119012201 | ACAGGTGGTATATGT[C/T]ATAAAACTTGTAAGA | 79836 |
rs778842256 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994611 | TTTCACCATGTTGGT[C/T]AGGCTGGTCTTGAAC | 79836 |
rs778885903 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118994178 | ATGAATGCTACGGTA[C/T]GGTACACCACATTTC | 79836 |
rs778919114 | snp | A/G | 0.000139567 | 0.0083525 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975607 | AGTTGGGTGAGTCCA[A/G]CGCGCTGCCGGGCCG | 79836 |
rs778938088 | in-del | -/AAG | 0.00528398 | 0.051128 | intron-variant | LONRF3 | GRCh38.p7 | X:119011127 | AAAAAAAAAAAAAAA[-/AAG]AAGAAAAAGAAAGAC | 79836 |
rs778948357 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118979643 | AGGGACATTAGAAAG[A/G]GGAAGGTGAGAGTGG | 79836 |
rs778958562 | snp | A/C | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973352 | CCAAGAGCCCGCAGG[A/C]TCTGAAGGCCAACTG | 79836 |
rs778988695 | snp | C/G | 6.32931e-05 | 0.00562517 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975459 | CCGCTGCGAGTCAAC[C/G]TGGTGCTCAGCGGCC | 79836 |
rs779009993 | snp | A/C | 0.00211696 | 0.0324653 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974041 | TCAGAAACCGAATTC[A/C]CCACCTTTGGGAGGC | 79836 |
rs779053254 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119007094 | TGAGGCAACATGCAG[C/G]TTTTTATGCAGTGTA | 79836 |
rs779119148 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976781 | GTTTGCCAGGAGCTC[A/G]GCCGTGGGGCGCGGT | 79836 |
rs779149397 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977455 | CTTTACCCTTCTAAG[A/G]GGAAAGGAGGCTCTC | 79836 |
rs779270674 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118996704 | AAGGCAGGCAGATCA[C/T]GAGGTCAGGAGATCC | 79836 |
rs779273612 | snp | A/G | 0.0026455 | 0.0362733 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018863 | CAGATGGCCGGGCAC[A/G]GTGGCTCACGCCTGT | 79836 |
rs779280647 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119004657 | TCCCCAGGTGACTGG[A/G]GGAGGCAGGAAGGAG | 79836 |
rs779304151 | snp | C/T | 2.46506e-05 | 0.00351065 | intron-variant | LONRF3 | GRCh38.p7 | X:119009294 | CTCATACCAGCTCAA[C/T]GAGAGCTGAATGTGC | 79836 |
rs779321955 | snp | C/T | 4.70046e-05 | 0.00484769 | stop-gained, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017682 | TTCATATCCCGAAAC[C/T]AAAACTAGTGAGTGG | 79836 |
rs779336314 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119014454 | GCCATTCAGCACATC[A/G]AATGCAGAGAGGAAG | 79836 |
rs779361009 | snp | G/T | 4.1542e-05 | 0.00455733 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974797 | TGGAGTCAGTACGGA[G/T]CGAACAGATGCTGAG | 79836 |
rs779437374 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119003845 | TTGTAGCTTTTTCCA[A/G]TAGAGGTCTCCTACA | 79836 |
rs779497124 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118993128 | TTCTAACACCCCCCC[C/G]CAAAAACCACACTAG | 79836 |
rs779499421 | in-del | -/AG | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118982704 | TTAGGGCTGTAGATA[-/AG]AGAGAGTCCTTTTAA | 79836 |
rs779606093 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999863 | TGCATACACTGCTAA[C/G]TTATAGCTGGCCTCT | 79836 |
rs779613047 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118999623 | GTGTAAGTTCTTTTG[C/T]TCCTCTGCTTTCTCC | 79836 |
rs779625928 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118983528 | AGTCGTTCCAACTCT[G/T]GGGTCCCAGCAGAAT | 79836 |
rs779636375 | snp | A/G | 2.90837e-05 | 0.00381327 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989670 | ATAAAGCCTCCAAGC[A/G]AGGTACTGGCTCTAC | 79836 |
rs779637728 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118985170 | TGCTTTGTTTCCTTT[C/G]ATTTCTCCCTTGGCC | 79836 |
rs779640893 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119000172 | TTGGGGGAGAGTGTC[-/T]TGAGAGTAAAGAAAG | 79836 |
rs779643460 | in-del | -/CCTT/CCTTCCTT | 0.0496549 | 0.149966 | intron-variant | LONRF3 | GRCh38.p7 | X:118978945 | ACGTTCTCTTTCTTC[-/CCTT/CCTTCCTT]CCTTCCTTCCTTCCT | 79836 |
rs779668230 | snp | C/T | 3.3588e-05 | 0.00409791 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974905 | CCCACCCAAAGGTGG[C/T]TGCAGAGGGCCCCGC | 79836 |
rs779733111 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118992256 | CCCAAATACTCTGGG[A/G]GGCAAATAGCCTCGG | 79836 |
rs779776902 | snp | A/C | 4.58022e-05 | 0.00478529 | missense, utr-variant-5-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118978446 | ATAGCATGTAAGCTC[A/C]GCCCGATGGGTTTTA | 79836 |
rs779799131 | in-del | -/TA | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118994749 | GACAAAGAGGGACAG[-/TA]TATATAATGGTAAAA | 79836 |
rs779807484 | snp | C/G | 0.000529661 | 0.016265 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974652 | CCGGCATGGAGCTCC[C/G]GGAGGCGCGGCAGGG | 79836 |
rs779839632 | snp | A/G | 0.000503556 | 0.0158595 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975644 | GGGCTCGGTGGCTAC[A/G]TGAGGGAGCGGGAGA | 79836 |
rs779903060 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:119007305 | TGAAGATAACAGCTC[C/T]AAAGGCCCCAGAAGA | 79836 |
rs779967193 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118981392 | CAGGAGGCTGAGGCC[A/G]GAGAATCGCTTGAAC | 79836 |
rs779974047 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119009478 | CTGAAGAAGCATAAG[C/T]GAAACCAGTGATGAG | 79836 |
rs780067069 | snp | C/T | 3.29663e-05 | 0.00405981 | intron-variant | LONRF3 | GRCh38.p7 | X:119009286 | TTGTTTCACTCATAC[C/T]AGCTCAATGAGAGCT | 79836 |
rs780070891 | snp | A/G | 2.39541e-05 | 0.0034607 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012003 | ATGCGAGCAAAGGGA[A/G]GTTGTGTAATGAGGG | 79836 |
rs780079039 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002290 | TGACTTTTATCTTGT[C/T]TCTCTTTTTAGCTTT | 79836 |
rs780120778 | snp | A/T | 2.39154e-05 | 0.00345791 | intron-variant | LONRF3 | GRCh38.p7 | X:119009100 | TTACCTAATTGCATA[A/T]TGTCTAATTGCCTCC | 79836 |
rs780151548 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974119 | GCTGGGACTGGGTTG[C/T]GTGTGTGTGGGGGGG | 79836 |
rs780171124 | snp | A/G | 3.33156e-05 | 0.00408126 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975334 | TGTGCCTGGAACGTG[A/G]GCGGGCCGCCGACCG | 79836 |
rs780255840 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119002834 | GATGGAGTCTCACTC[C/T]GTTGCCCAGGCTGGA | 79836 |
rs780269655 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119004738 | TATCTTGATTGTGGC[A/G]ATGGTTTCATAAGTG | 79836 |
rs780382248 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118980804 | GGCTAAGGAACTTGA[C/T]AGTGTGGTGAGAAGC | 79836 |
rs780418381 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119010490 | CTAGAAATCGTTTTT[A/T]TTTTCTCATTAATTT | 79836 |
rs780471162 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119011196 | CTGGTAATGTGGTGT[C/T]CAAGTCATCTTGATT | 79836 |
rs780518890 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013849 | TCCTGTGTCTTTTCC[A/G]GCAAGTAATGAGAAA | 79836 |
rs780520037 | snp | A/C | 6.5619e-05 | 0.00572758 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975442 | GGCAGCAGCCGCCGC[A/C]GCCGCTGCGAGTCAA | 79836 |
rs780552929 | snp | C/T | 2.42052e-05 | 0.00347879 | intron-variant | LONRF3 | GRCh38.p7 | X:119014382 | ATGTCTATTTTTAAA[C/T]GGGTTGTCCCACTAG | 79836 |
rs780594430 | in-del | -/T | 0.000397679 | 0.0140954 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012862 | CGAATACATTACGAA[-/T]TTTTTTTCTTCACAC | 79836 |
rs780657799 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981930 | AGGGAGCAGGCCACT[A/G]GGTGGAGGGACGTCC | 79836 |
rs780665519 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118984551 | GTCTCTCCAGTCTGC[C/T]TTTATAGAGAAACTG | 79836 |
rs780667150 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119014964 | CTGTTAGTTGAGTTA[C/T]ACTAGACAGTAGTTT | 79836 |
rs780667686 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976814 | CTGGCGAAGCATGCC[A/G]GGGAGGAGGCAGCAG | 79836 |
rs780691281 | snp | G/T | 2.30391e-05 | 0.00339397 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017647 | AGGACAGACTGAATG[G/T]TATTCGACGAGTCCT | 79836 |
rs780710941 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973099 | TGTTCTCTGGGACCT[C/T]GGTGTTGATCTAAGA | 79836 |
rs780718721 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118977534 | CACCTTCAGAAAAAG[G/T]AACCTGCTCCCCACA | 79836 |
rs780727855 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118993891 | TCCTCAAGCAAAACA[A/G]TTACCAGCCAAGAAT | 79836 |
rs780758269 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119014568 | TAAAGTAAAGCAGTA[-/G]GAACTTGGATCCAAG | 79836 |
rs780765263 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999753 | GTTGGCTCACTCGAA[A/G]TTTAAAAGCCATCAT | 79836 |
rs780861365 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118998336 | ATGAGATTGGAGACT[A/G]TTTTAAGTGATGTAA | 79836 |
rs780933509 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119009306 | CAATGAGAGCTGAAT[A/G]TGCACATTACTTCCC | 79836 |
rs781007753 | in-del | -/TT | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:118979300 | AGCCACCGCGCTGGC[-/TT]TTTTTTTTTTTGAGA | 79836 |
rs781038309 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118983922 | GGAAGTTGCTTTGAA[C/T]TGGTTTGAGTATGTG | 79836 |
rs781050319 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:118978969 | CCTTCCTTCCTTCCT[C/T]TCTCTCTCTCTCTCT | 79836 |
rs781084025 | snp | G/T | 4.26876e-05 | 0.00461974 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974794 | CCATGGAGTCAGTAC[G/T]GATCGAACAGATGCT | 79836 |
rs781098454 | in-del | -/AAT | 0.00105904 | 0.0229869 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017854 | TAGAAAGACCAAAAG[-/AAT]AATGTGACCTATTTG | 79836 |
rs781170861 | snp | C/T | 4.72886e-05 | 0.00486231 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011991 | AAGTGAGGAGCCATG[C/T]GAGCAAAGGGAGGTT | 79836 |
rs781211607 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118987009 | CTGTTGGCACCTCAC[C/T]CTAGATTAAAGGAAA | 79836 |
rs781218952 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119007841 | TACTGAAATAATACA[G/T]CTGTGTTGTTGTAGC | 79836 |
rs781241937 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975695 | GGATTTGGACCAGGG[C/T]AGAAGAGGGGGCGGG | 79836 |
rs781345232 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118977869 | TGCTGGGCTTTGTAG[A/C]CAAAGGTGTTACTAA | 79836 |
rs781384606 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118990904 | GCTCTGTTGCCCAGG[C/T]TGGAGTGCAGTGGTG | 79836 |
rs781404490 | in-del | -/T | 0.0018748 | 0.0305596 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974754 | CGGTCCCTAGACGCC[-/T]TCGTCTCCTCCCGTG | 79836 |
rs781411925 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018176 | TAATAATTTATTTTT[G/T]GCACTACTGTATCCT | 79836 |
rs781439127 | snp | A/C | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974519 | CTGTTACAAAACTGT[A/C]TGGTTTTGTAACAAT | 79836 |
rs781448161 | in-del | -/AAC | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118995515 | ACTAAATTAAATTGA[-/AAC]AACAACAACAATACA | 79836 |
rs781451067 | snp | A/G | 2.27936e-05 | 0.00337584 | synonymous-codon, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982868 | CCTAGGCAAGGTGGA[A/G]GAGGCACTAAGGGAG | 79836 |
rs781460875 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012367 | TACCTCATTGGGTTT[A/G]CTTGGAAGATTGGTG | 79836 |
rs781512405 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002491 | ATAATATCCCATTAT[A/G]TGAATCCACCACAGT | 79836 |
rs781551230 | snp | C/T | 0.0003221 | 0.0126865 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975318 | CACACCTTTTGTAAA[C/T]TGTGCCTGGAACGTG | 79836 |
rs781554658 | snp | A/T | 0.00422943 | 0.0457911 | intron-variant | LONRF3 | GRCh38.p7 | X:119001747 | AGCTTTTGCTAAGAG[A/T]TTGCTGTGTCCTTTT | 79836 |
rs781570476 | snp | C/T | 3.99553e-05 | 0.00446946 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975156 | CTGGCGCCGGCGCCC[C/T]CGGACGAGGGTAGCA | 79836 |
rs781613354 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118998823 | CAGCCTCCTGCCTGG[A/C]AAATTTTTGTATTTT | 79836 |
rs781677803 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119001959 | TCATCTTCATCATTA[A/G]TACCATCAAATAATA | 79836 |
rs781679760 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118998289 | ATGCAGCCATAAAAA[A/G]GAATAAGTTAACAGC | 79836 |
rs781680171 | snp | A/C | 4.64733e-05 | 0.00482021 | intron-variant | LONRF3 | GRCh38.p7 | X:119006271 | TGTTTGGTTTAAATC[A/C]GTATTTCTTTCTTGT | 79836 |
rs781745798 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987206 | TTGAGTCACTAGTGG[C/T]TCTGTTCTTTGCAAA | 79836 |
rs781774490 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118985644 | AGGAGAGAAAGGCTT[A/G]CATCTGTGACACATT | 79836 |
rs796161558 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118978141 | CAAAAATGACTTTGC[A/G]GTTGGGGAACCTCAG | 79836 |
rs796454597 | in-del | -/TT | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994409 | ATCAGACAAAACAAA[-/TT]TTTTTTTTTTTGAGA | 79836 |
rs796479755 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000390 | AAAGAGTGAATGGAA[A/C]AATAATCGGAGGTGT | 79836 |
rs796674247 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119001091 | GTAAAATGTTTTTTG[C/T]GTGAAAATCTGGCCC | 79836 |
rs796899027 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119011483 | AGAGCATGAAAGTAA[G/T]AAAAAATATGAATTA | 79836 |