SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1106361 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571279 | AGCTCTGTCCAAAGC[A/G]GACGGGAGGCGGCTC | 55666 |
rs1122424 | snp | C/T | 0.267908 | 0.249358 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593468 | tcctatcactttccc[C/T]tgatgttacagttag | 55666 |
rs3087664 | snp | A/G | 0.499767 | 0.0107802 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558836 | ACAAGGGGGTAACCA[A/G]GAGCTCCCAGCCAGA | 55666 |
rs3208785 | snp | C/G | 0.49949 | 0.0159663 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558922 | CGCACAGGGAGGGGC[C/G]GATGCTGCCACCACC | 55666 |
rs3208787 | snp | C/T | 0.418491 | 0.184691 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558634 | CTGCATTGGTTATAA[C/T]AACAGTTATCAGTAA | 55666 |
rs3922945 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569296 | AAACGAACACTTGGA[A/T]ACTCCGCCATCCTGG | 55666 |
rs3923206 | snp | G/T | 0.24932 | 0.249999 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594962 | tttttgtgttttttt[G/T]tttgtttgtttgttt | 55666 |
rs3923207 | snp | C/T | 0.251859 | 0.249993 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594951 | ttttttttgtttgtt[C/T]gtttgttttgagaca | 55666 |
rs3934711 | snp | A/G | 0.331106 | 0.236478 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565628 | AGAAGCCAAAAGGAA[A/G]GTTCCTCTTCGCTGT | 55666 |
rs3935538 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566301 | tctgttgcccagacc[A/G]gagtgcattggcgca | 55666 |
rs3935539 | snp | A/G | 0.140919 | 0.224948 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566285 | gagtgcattggcgca[A/G]tcttggcttactgca | 55666 |
rs3935540 | snp | C/G | 0.0894459 | 0.191631 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566218 | cagcctcccgagtag[C/G]tgggattacaggtgc | 55666 |
rs3935543 | snp | A/G | 0.45889 | 0.13735 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612848 | ATTTTGACCTGCCAC[A/G]CTAGTGTGCGCTCTC | 55666 |
rs3936237 | snp | C/T | 0.328148 | 0.237472 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566238 | ttcaagcgattctcc[C/T]gcctcagcctcccga | 55666 |
rs4072446 | snp | C/T | 0.0505692 | 0.150756 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558802 | CTCACAGGCAGGGTG[C/T]CTGCCACCAAGCAGT | 55666 |
rs4073997 | snp | C/G | 0.404136 | 0.199228 | synonymous-codon, nc-transcript-variant, missense | NPLOC4 | GRCh38.p7 | 17:81559376 | TCTCCATGAGTACGG[C/G]GCCGTCGGGGGCTCC | 55666 |
rs4074915 | snp | A/G | 0.456095 | 0.141508 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612204 | CTGGTTTACGAGGGC[A/G]CCGGCGGCCGTCCCT | 55666 |
rs4074916 | snp | A/G | 0.459004 | 0.137176 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612222 | GGCGGCCGTCCCTCC[A/G]GGGCTCAGTCAGACC | 55666 |
rs4076819 | snp | C/G | 0.377977 | 0.21476 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559543 | CCACCCAGTGCTGGT[C/G]CTGCCCACACAGCAC | 55666 |
rs4078371 | snp | G/T | 0.25634 | 0.24992 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579824 | TCCTTTGCTCTCCCT[G/T]GCAGTGAAACCCCCC | 55666 |
rs6565596 | snp | G/T | 0.479583 | 0.0989539 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558092 | CCCGGGTAAGAGCCA[G/T]GCCCCGGCCTGGCCA | 55666 |
rs6565597 | snp | C/T | 0.361894 | 0.223562 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559795 | tggagtgcagtggca[C/T]gatctcggctcactg | 55666 |
rs6565598 | snp | A/T | 0.0777841 | 0.181223 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572183 | TTTATTTAATTAATT[A/T]ATTTATTTATTTATT | 55666 |
rs6565599 | snp | C/G | 0.256619 | 0.249912 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588133 | cactgtagaagtcca[C/G]atcaacgaatgtgaa | 55666 |
rs6565601 | snp | C/T | 0.45889 | 0.13735 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613147 | AAAAAAAACAAAAAC[C/T]GATAAAAAGCTAACA | 55666 |
rs6565602 | snp | C/T | 0.363359 | 0.222822 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619833 | gcagtgagctgagat[C/T]gcgccactgcactcc | 55666 |
rs6565603 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620609 | TTGCAATGGTGACAC[A/G]TAAGGTTCATCCATC | 55666 |
rs6565604 | snp | A/G | 0.495546 | 0.0469789 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622216 | GGCTGTTATCTCTCC[A/G]GTCTTGTTTCTATTG | 55666 |
rs6565605 | snp | C/T | 0.466308 | 0.125343 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622333 | TAAAGTATCACTACA[C/T]ATACCATACACGCCA | 55666 |
rs6565606 | snp | A/G | 0.489665 | 0.0711382 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622345 | ACATATACCATACAC[A/G]CCAGACACTACTAGA | 55666 |
rs6565607 | snp | C/T | 0.459233 | 0.136827 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623654 | atacaaaaaattagc[C/T]gggcgtggtggtggg | 55666 |
rs6565608 | snp | C/T | 0.459233 | 0.136827 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623722 | agagtggcgtgaacc[C/T]gggaggcggagcttg | 55666 |
rs6565609 | snp | A/G | 0.488666 | 0.0744214 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625241 | taacacctgtgcagg[A/G]accatgaaaggaaag | 55666 |
rs6565610 | snp | A/G | 0.363359 | 0.222822 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625626 | gtcccagcaactcgg[A/G]aggctgaggtggaag | 55666 |
rs6565611 | snp | C/T | 0.364193 | 0.222396 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631293 | ctcacacctataatc[C/T]gtgcacttcaggaga | 55666 |
rs6565612 | snp | C/T | 0.485799 | 0.0830599 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635794 | TTCACCCAATACTGC[C/T]AAGCTTCCCCCAGAA | 55666 |
rs6565613 | snp | C/G | 0.492188 | 0.0620098 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636190 | TGGCCAGGATGGTCT[C/G]GAACTCCTGACCCCA | 55666 |
rs6565614 | snp | C/G | 0.441295 | 0.160954 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638369 | agtggcgcgatctcg[C/G]ctcactgcaaccttc | 55666 |
rs6565615 | snp | A/G | 0.441295 | 0.160954 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638589 | tagacgtgagccacc[A/G]tgcccggctggggat | 55666 |
rs7208045 | snp | A/C | 0 | 0 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560846 | gtacgagagtcccag[A/C]tgcttcacatcttca | 55666 |
rs7208474 | snp | A/G | 0.0182399 | 0.0937403 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600327 | CCCTGCTTGGCTGCC[A/G]GATGCCTCAGTACCT | 55666 |
rs7209180 | snp | A/C | 0.458775 | 0.137524 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614493 | GCCATCATCACCACC[A/C]CCCAAAAAGGCCCAC | 55666 |
rs7213129 | snp | C/T | 0.458775 | 0.137524 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614547 | CTTCTAAAGGGCAAA[C/T]TCCCAGGAGTCAGAC | 55666 |
rs7213849 | snp | C/T | 0.361684 | 0.223667 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600584 | AACACATGCGACACG[C/T]CTCCCGGCTTCTCTC | 55666 |
rs7214251 | snp | C/T | 0.24932 | 0.249999 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600266 | ACAGCCCGGCCACTC[C/T]CCCAACTCCCCCTGG | 55666 |
rs7217444 | snp | C/G | 0.0581099 | 0.160244 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567903 | caacatggcgaaacc[C/G]cgtctctactaaaaa | 55666 |
rs7219915 | snp | C/T | 0.364193 | 0.222396 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624787 | AGCGGTGGGTAAGCC[C/T]GCCACACGCGAGCTG | 55666 |
rs7220155 | snp | C/T | 0.441295 | 0.160954 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638994 | tgcaaagggctgtta[C/T]catctttgtttcaaa | 55666 |
rs7220310 | snp | A/C | 0.488726 | 0.0742286 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81639030 | actataaactaagcg[A/C]ctcccgaagttattt | 55666 |
rs7221003 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603775 | CAAGTGTATTACAGA[C/T]ATAAATGTACTTCTC | 55666 |
rs7222241 | snp | C/G | 0.459004 | 0.137176 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607688 | CTTGACCTAGACTGA[C/G]AAAGGCTGACCAAGT | 55666 |
rs7223613 | snp | C/T | 0.459004 | 0.137176 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607777 | CCCACTGACAAGCAA[C/T]AGTGGGTTTCTAGCA | 55666 |
rs7405450 | snp | C/T | 0.4944 | 0.0526182 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573423 | AAACCAAGTCCATTA[C/T]CCTAATGAGAAGCCC | 55666 |
rs7405454 | snp | A/G | 0.327914 | 0.237549 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581539 | CTTGGCATAGGTGCG[A/G]GCAGTGAGGAGACAA | 55666 |
rs7405469 | snp | C/G | 0.48995 | 0.0701706 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599570 | TTTGCAGTCTCACCC[C/G]CTTCATCTGTAGAGA | 55666 |
rs7405578 | snp | A/C | 0.364401 | 0.222289 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621280 | AGTAGGTGCCCAATA[A/C]ATCTTTGTTAAGAAC | 55666 |
rs7405605 | snp | C/T | 0.257176 | 0.249897 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577681 | TCCATCTTCAAACTC[C/T]GCGTGCTGGCACCTG | 55666 |
rs7405646 | snp | A/G | 0.491157 | 0.065903 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584038 | ATATGCCCTTGGGAC[A/G]GGGCTTTTCAATTGT | 55666 |
rs7405814 | snp | C/T | 0.491157 | 0.065903 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618255 | ctaggaagtgaggag[C/T]gtctctgcccggccg | 55666 |
rs7405864 | snp | C/T | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581982 | CTGACAGCAGAGACA[C/T]GCTTCCATGGTGGAC | 55666 |
rs7405901 | snp | C/T | 0.459233 | 0.136827 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620787 | GGCTGGAACAGAGAG[C/T]GTGCACTCACAGTCA | 55666 |
rs7405937 | snp | A/G | 0.486067 | 0.0822953 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630785 | ggggagctgaggcac[A/G]aggatcacttaaacc | 55666 |
rs7405966 | snp | G/T | 0.48995 | 0.0701706 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599701 | TTCATGGCTCTACAT[G/T]AATTTATTAAAATTG | 55666 |
rs7406003 | snp | C/T | 0.439363 | 0.163222 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630571 | caacgccAGCTATTA[C/T]TTACTTTCCCTAAAA | 55666 |
rs7406040 | snp | A/C | 0.363985 | 0.222503 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630557 | acaggtgtgagccac[A/C]acgccAGCTATTACT | 55666 |
rs7406089 | snp | C/T | 0.441295 | 0.160954 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638125 | TTGCTCAGGGTGCCA[C/T]tgtaactacccaaca | 55666 |
rs7406136 | snp | A/G | 0.267636 | 0.249377 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594034 | atcccagcaccttgg[A/G]aggccgaggcgggcg | 55666 |
rs7406296 | snp | A/G | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585523 | aaaagttagccaggc[A/G]tggtggtgcacacct | 55666 |
rs7406360 | snp | A/G | 0.364609 | 0.222182 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624519 | caggagaatcacttc[A/G]acctgggaggcggag | 55666 |
rs7406382 | snp | C/T | 0.486067 | 0.0822953 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630760 | cgtacgcctatggtc[C/T]cagctacttggggag | 55666 |
rs7406408 | snp | A/G | 0.4944 | 0.0526182 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568506 | GATTTAAGAACAACC[A/G]TGTGTACACAGCCTG | 55666 |
rs7406417 | snp | A/C | 0.431769 | 0.17164 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585803 | accagcctgggcaac[A/C]tggtgaaatcctgat | 55666 |
rs7406463 | snp | C/T | 0.24932 | 0.249999 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594080 | agatcgagaccatcc[C/T]ggctaacacggtgaa | 55666 |
rs7406465 | snp | C/T | 0.441295 | 0.160954 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638259 | ctactcaaaaaaaat[C/T]agtgtccttgagaat | 55666 |
rs7406662 | snp | A/G | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589715 | ACTTTTGAAAAAAAG[A/G]AAAGAAAAGGCTCAG | 55666 |
rs7406667 | snp | A/G | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599244 | cagtgagccaagatc[A/G]tgccactgcactcca | 55666 |
rs7406680 | snp | A/G | 0.249038 | 0.249998 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577684 | ATCTTCAAACTCTGC[A/G]TGCTGGCACCTGGAC | 55666 |
rs7406704 | snp | C/T | 0.331411 | 0.236373 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568145 | CATGGAAATGCGCCC[C/T]GGTCCCCCGGTGGAG | 55666 |
rs7406753 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607635 | GAATCTGCATGCTAA[C/G]AGCAGCCACAAACAC | 55666 |
rs7406756 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608372 | CTGCACTGTGGCCAC[A/G]CAGCCAGGCGCCTGC | 55666 |
rs7406829 | snp | A/T | 0.267636 | 0.249377 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593036 | CTCAGAATAAAATAG[A/T]CATTAAAACCACACT | 55666 |
rs7406859 | snp | A/G | 0.25634 | 0.24992 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577817 | ACCTGCCAGGCCTCC[A/G]AACCTCTCAGTCCCA | 55666 |
rs7406863 | snp | C/T | 0.495927 | 0.0449436 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593382 | GGCCAGTACGGATCC[C/T]GCTGTGCTGTCCTCA | 55666 |
rs7406991 | snp | C/G | 0.491263 | 0.0655142 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581588 | GCAGCCAGTCCTCCA[C/G]AGCACCAAGGCCACC | 55666 |
rs7501521 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560623 | gaggaaggagaatgg[C/T]gtgaacctgggaggc | 55666 |
rs7502085 | snp | A/G | 0.327914 | 0.237549 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583177 | TATCTATCAAAACTC[A/G]AAAAACCTTCCTCCC | 55666 |
rs7502153 | snp | C/T | 0.106633 | 0.204807 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560512 | aagagatggagacca[C/T]cctggctaacatggt | 55666 |
rs7502281 | snp | A/C | 0.256061 | 0.249927 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591681 | CATGCAGCAGCAGGA[A/C]ATACATGTCCTGATG | 55666 |
rs7502337 | snp | C/T | 0.494442 | 0.0524218 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621444 | CCACCACTGAGCCAG[C/T]GGCCACAGCACATGC | 55666 |
rs7502346 | snp | C/T | 0.364401 | 0.222289 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636715 | GGGTCGTAAGTCCCC[C/T]GGGGAGGGACACGGA | 55666 |
rs7502883 | snp | C/T | 0.365024 | 0.221967 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621531 | TAAGGCACATGTGAG[C/T]AAGTGCCCAGATGGT | 55666 |
rs7503152 | snp | C/T | 0.102014 | 0.201495 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616001 | ctgtgccaacaaaag[C/T]aaatgcaaacctctg | 55666 |
rs7503221 | snp | A/C | 0.262435 | 0.249691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616345 | aaaaaaaaagaaaag[A/C]aaagctgctaaatct | 55666 |
rs7503280 | snp | A/C | 0.248755 | 0.249997 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602155 | ctcagtggcatacac[A/C]gatagtcccagctac | 55666 |
rs7503288 | snp | A/G | 0.102014 | 0.201495 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616303 | tccagcctgggcgac[A/G]tagcaagactctgtc | 55666 |
rs7503301 | snp | A/C | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616333 | ctcaaaaaaaaaaaa[A/C]aaaaagaaaagcaaa | 55666 |
rs7503328 | snp | A/G | 0.459004 | 0.137176 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616502 | ttgggaggccgaggc[A/G]ggaggatcatgaggt | 55666 |
rs7503679 | snp | C/G | 0.45866 | 0.137698 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616817 | ACTGCCAAAGACTCA[C/G]ACACAGAAATTATGA | 55666 |
rs7503824 | snp | G/T | 0.084728 | 0.187577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616172 | aaataaaaaaaaaaa[G/T]tagccgggggtggtg | 55666 |
rs7503853 | snp | C/T | 0.102014 | 0.201495 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616304 | ccagcctgggcgaca[C/T]agcaagactctgtct | 55666 |
rs7503870 | snp | C/T | 0.458775 | 0.137524 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616315 | gacatagcaagactc[C/T]gtctcaaaaaaaaaa | 55666 |
rs7503894 | snp | C/T | 0.26271 | 0.249677 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616447 | TAGAAGAGTAACACA[C/T]Gggccaggcacagtg | 55666 |
rs7503932 | snp | C/T | 0.104859 | 0.203554 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602158 | agtggcatacaccga[C/T]agtcccagctacttg | 55666 |
rs7504011 | snp | A/C | 0.102014 | 0.201495 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625519 | ctagaactgaaaaac[A/C]caagaacagaaataa | 55666 |
rs7504057 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560639 | gtgaacctgggaggc[A/G]gaggttgcagtgaac | 55666 |
rs8064538 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569558 | CGTGTCATTGGATTC[A/G]GAGGGCAAATGAGCA | 55666 |
rs8067735 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602910 | acacatacatacata[C/T]atatgtatatataca | 55666 |
rs8067862 | snp | C/T | 0.14933 | 0.228835 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602952 | atatatacacacaca[C/T]atatatacacacata | 55666 |
rs8067866 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602954 | atatacacacacata[C/T]atatacacacatata | 55666 |
rs8067873 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602968 | atatatacacacata[C/T]atatacacaaataca | 55666 |
rs8068081 | snp | C/T | 0.0836354 | 0.186609 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557856 | GTGTCCCATGCCAGG[C/T]GGACCTGGAGGTGTC | 55666 |
rs8068511 | snp | A/T | 0.496517 | 0.0415876 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557764 | CCTGACCCTCCACAA[A/T]AGCTCTGCCGTGACC | 55666 |
rs8069008 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558050 | GGCCATCATTAAGGC[A/G]AAGAAGCATCGAGAT | 55666 |
rs8070929 | snp | G/T | 0.392361 | 0.205507 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563967 | acatctgtaatccca[G/T]ctactcgggaggctg | 55666 |
rs8071190 | snp | A/C | 0.462253 | 0.132093 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591987 | TGTCCTTCCACAGGG[A/C]CCCTCAGGGTCACTC | 55666 |
rs8074214 | snp | A/G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622794 | gacctcaggtgatcc[A/G/T]cccaccttggcctcc | 55666 |
rs8074989 | snp | C/G | 0.364193 | 0.222396 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631702 | CAGACAGGAACATGC[C/G]CATAAGTGTCCTAGC | 55666 |
rs8075102 | snp | G/T | 0.49423 | 0.0534032 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591950 | GCCCAGCCCAGTGTG[G/T]GGGGTAAGTTCTACA | 55666 |
rs8075338 | snp | A/G | 0.362104 | 0.223456 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563306 | tctcaatcccttgac[A/G]ttgtgatccacctgc | 55666 |
rs8075348 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622792 | ctgacctcaggtgat[A/C]cgcccaccttggcct | 55666 |
rs8075598 | snp | C/T | 0.458775 | 0.137524 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623580 | gaggcaggcggatca[C/T]gaggtcaggagatcg | 55666 |
rs8076150 | snp | A/G | 0.25634 | 0.24992 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577137 | GGGTTCCTCAGAGAT[A/G]CCCTCTGGCCCCTCC | 55666 |
rs8076879 | snp | G/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638427 | cctcagcctcccggg[G/T]agctgggactacagg | 55666 |
rs8077038 | snp | G/T | 0.364401 | 0.222289 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610101 | AATAGGTAAGTTCTT[G/T]GAACCACTCACTACA | 55666 |
rs8079542 | snp | G/T | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576903 | TGCAAGTGTCCACCC[G/T]GCCACATTCCCAGAG | 55666 |
rs8079963 | snp | C/T | 0.486133 | 0.082104 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636259 | CACAGGCGTGAGCCA[C/T]TGCGCCGGGCCGACA | 55666 |
rs8080391 | snp | A/T | 0.364817 | 0.222075 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599293 | gactccTCAAAaaaa[A/T]aaaataaaataaaat | 55666 |
rs8080837 | snp | A/G | 0.031825 | 0.122064 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603042 | gacatggtggtgcac[A/G]cctgtagtcccagac | 55666 |
rs8081026 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632558 | acctcaagttatcca[C/T]ccacctgggcctccc | 55666 |
rs8081701 | snp | C/T | 0.262435 | 0.249691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632415 | cctccccggttcaag[C/T]gattctcctgtctca | 55666 |
rs8081790 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602926 | atatgtatatataca[C/T]acacacatatatata | 55666 |
rs8081808 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602960 | acacacatatatata[C/T]acacatatatataca | 55666 |
rs8081883 | snp | C/T | 0.494315 | 0.0530107 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573572 | TTCTACTCTCTCCCC[C/T]TTCCTCACTATTGTA | 55666 |
rs8082090 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595532 | tatacatatatatat[A/T]tattttttttttctt | 55666 |
rs8082093 | snp | A/T | 0.33875 | 0.233717 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595534 | tacatatatatatat[A/T]ttttttttttctttt | 55666 |
rs8082297 | snp | A/G | 0.24932 | 0.249999 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605198 | aggcaggagaatggc[A/G]tgaacccgggaggtg | 55666 |
rs9319619 | snp | A/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622623 | TGGCATGATCTCGGC[A/T]TACTGCAACCTCCAC | 55666 |
rs9674738 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558049 | TGGCCATCATTAAGG[C/G]AAAGAAGCATCGAGA | 55666 |
rs9674872 | snp | A/T | 0.45889 | 0.13735 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614905 | ACACACAGGGGACAG[A/T]CTGAGAGGGCAGGAT | 55666 |
rs9709130 | snp | C/T | 0.488786 | 0.0740357 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616922 | TCCAAAATGACCAGG[C/T]GGGATTCTAGGACAT | 55666 |
rs9709360 | snp | C/T | 0.084728 | 0.187577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616445 | TGTAGAAGAGTAACA[C/T]ACGggccaggcacag | 55666 |
rs9747093 | snp | A/G | 0.464309 | 0.12873 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617254 | AGACAGATTTAGGGG[A/G]AAAAAAAATCAGATT | 55666 |
rs9747336 | snp | C/T | 0.363359 | 0.222822 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617163 | TTCACTGGAGGCCAG[C/T]GGGCCAATGTGGCAG | 55666 |
rs9747349 | snp | C/T | 0.45866 | 0.137698 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617271 | AAAAAAATCAGATTA[C/T]GTATTTATTTATATA | 55666 |
rs9748176 | snp | C/G | 0.458775 | 0.137524 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617017 | CATGCCAGGTCCCAC[C/G]GATGCATCTACAGCA | 55666 |
rs9748184 | snp | A/G | 0.439502 | 0.163061 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629254 | TTGGAGTGCAGTGGC[A/G]CCACCTCGACTCACT | 55666 |
rs9889473 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623507 | tctgtctcaaaaaaa[A/T]aaaaaaCCCggccgg | 55666 |
rs9889642 | snp | C/T | 0.458084 | 0.138567 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624736 | ATGGGAGGCTAGAAG[C/T]CTCTCTGAAGAGCTT | 55666 |
rs9890121 | snp | C/T | 0.25634 | 0.24992 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564719 | tttgaacccaggagg[C/T]ggaggttgcagtgag | 55666 |
rs9890842 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574767 | gcctgtaatcccagc[A/G]ctttgggaggccgag | 55666 |
rs9890852 | snp | C/T | 0.492484 | 0.0608394 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633084 | GTGGTGAGCAGATCG[C/T]GCCACTGCACTCCAG | 55666 |
rs9892655 | snp | C/G | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582047 | GAGGGCTCCTCTGTA[C/G]CAAAGAACACCCGAG | 55666 |
rs9893343 | snp | A/G | 0.24932 | 0.249999 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574700 | GAAATCCAGGGATCG[A/G]TGTCTTTGTTAGCTC | 55666 |
rs9893365 | snp | A/T | 0.494651 | 0.0514399 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574529 | TGCGCTGGGAGGAGG[A/T]TGTCTTAATTCTAAG | 55666 |
rs9893500 | snp | C/G | 0.0422008 | 0.138995 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605245 | gagatggcgccactg[C/G]actccagcctgggcg | 55666 |
rs9894429 | snp | C/T | 0.493944 | 0.0546949 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81629785 | CCGCTTCACTCCATC[C/T]GGGGACTGGACACGA | 55666 |
rs9895132 | snp | A/C | 0.257454 | 0.249889 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569875 | AATCAATAGAAATAC[A/C]ACTTTTATTCTTCGT | 55666 |
rs9895741 | snp | A/G | 0.262435 | 0.249691 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636805 | CCCTGGCGAGAGAAG[A/G]GAAAGGGGCCGAGTC | 55666 |
rs9898926 | snp | A/G | 0.24932 | 0.249999 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575803 | TCTCCCACCTCCACC[A/G]CAAGGGAAGATGCAA | 55666 |
rs9899035 | snp | A/G | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597507 | tacagaaattaggcc[A/G]ggtgcggtggctcac | 55666 |
rs9899227 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621779 | CTACAGGGTGGCATG[C/G]GCCACTGCAGTGGCA | 55666 |
rs9899778 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582713 | tagtcTATTAGTATT[C/G]TTTTTAAAGGAAAAG | 55666 |
rs9900215 | snp | A/G | 0.46014 | 0.13543 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588539 | TTTTTGTAGAGACAC[A/G]GTCTCGCTATGTTGC | 55666 |
rs9901054 | snp | A/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597341 | AGGAAAGTAGCTTTT[A/T]AACATCTCCTCAAGA | 55666 |
rs9901933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571140 | TTGGAATGGTGCATC[A/G]ATGGGCTTGGCTCGT | 55666 |
rs9902146 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571258 | CGTGGCAGCAGCATA[A/G]GAAATGAGCCGCCTC | 55666 |
rs9903547 | snp | A/G | 0.491885 | 0.0631791 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623739 | ggaggcggagcttgc[A/G]gtgagccgagatcgc | 55666 |
rs9903803 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571281 | GCCGCCTCCCGTCCG[C/G]TTTGGACAGAGCTCC | 55666 |
rs9903882 | snp | C/G | 0.24932 | 0.249999 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580420 | GCAGCCAGAGTGATC[C/G]TCTCACAGCCCCGGC | 55666 |
rs9904579 | snp | A/G | 0.257454 | 0.249889 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571252 | TCCTGGCGTGGCAGC[A/G]GCATAGGAAATGAGC | 55666 |
rs9904587 | snp | A/G | 0.252983 | 0.249982 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571255 | TGGCGTGGCAGCAGC[A/G]TAGGAAATGAGCCGC | 55666 |
rs9905026 | snp | C/T | 0.327914 | 0.237549 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564546 | tgtaatcccaacact[C/T]tgggaggcagaggca | 55666 |
rs9905786 | snp | G/T | 0.261884 | 0.249717 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635037 | tctctataaaaaaaT[G/T]TTTTTAATTAAAAAG | 55666 |
rs9905956 | snp | C/T | 0.0236746 | 0.106192 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558985 | GTCTTTCCAACACGG[C/T]GGGGGACTTGTCAAC | 55666 |
rs9907417 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592805 | cctggccaacatggt[A/G]aaaccccgtctctac | 55666 |
rs9907670 | snp | A/G | 0.24932 | 0.249999 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592909 | GAATCATTTGAACCC[A/G]GAGGCAGAAGTTGCA | 55666 |
rs9907680 | snp | C/T | 0.00317404 | 0.0397107 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606653 | ATATCCGTTTCTCAG[C/T]CATGAAAACAAATCT | 55666 |
rs9909330 | snp | A/G | 0.256061 | 0.249927 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564703 | tgaggcaggagaatc[A/G]tttgaacccaggagg | 55666 |
rs9909675 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586513 | tactcgggaggctga[C/G]gcacaagaatcgctt | 55666 |
rs9910624 | snp | C/T | 0.24932 | 0.249999 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586205 | AAGCCCCTTCCCTCC[C/T]CTCCTGCAGGAAGTG | 55666 |
rs9911342 | snp | C/T | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586566 | agtgggccgagatcg[C/T]gccactgtactccag | 55666 |
rs9911375 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619836 | gtgagctgagatcgc[A/G]ccactgcactccagc | 55666 |
rs9911383 | snp | A/G | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574090 | CAAAAATCAAATCCA[A/G]TCAAACTAAATCACC | 55666 |
rs9911460 | snp | A/T | 0.42574 | 0.177808 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571815 | AAACAAAAAGCCCTT[A/T]AAACTGTGAGCATTT | 55666 |
rs9911739 | snp | C/G | 0.321769 | 0.239477 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565083 | AGTGTCCACCAGCAA[C/G]AACATGGATGCTGCA | 55666 |
rs9911829 | snp | A/G | 0.25214 | 0.249991 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564743 | cagtgaggcaagatc[A/G]cgccaccacactcca | 55666 |
rs9912074 | snp | A/G | 0.327914 | 0.237549 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564862 | TGTGTTAACAGAAGG[A/G]TTCTAGCATTTGTCC | 55666 |
rs9912384 | snp | C/T | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580488 | TCTCACTTCCAACCA[C/T]AGATTCAGCTTCCAA | 55666 |
rs9912938 | snp | C/T | 0.493925 | 0.054776 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581280 | cttgaacctgggagg[C/T]ggaggttgtagtgag | 55666 |
rs9913546 | snp | A/C | 0.327211 | 0.237778 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604365 | ATCCTTAGTAACATA[A/C]ACTGAAGGTTTTAGG | 55666 |
rs9913794 | snp | C/T | 0.337841 | 0.23406 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597910 | ccatcctggctaaca[C/T]ggtgaaatcccgtct | 55666 |
rs9914232 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635036 | atctctataaaaaaa[A/T]GTTTTTAATTAAAAA | 55666 |
rs9914540 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620469 | tcattgcactccagc[C/G]tgggcgacagagcga | 55666 |
rs9914834 | snp | A/G | 0.250168 | 0.25 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569494 | TGACAGGAAAGGAAC[A/G]GAAGGGCCAGGAGGC | 55666 |
rs9914952 | snp | A/C/T | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635351 | ctcaaaaaaataaaa[A/C/T]aaggttaaaaaaaaa | 55666 |
rs9915143 | snp | A/C | 0.251296 | 0.249997 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599091 | gtcgagagttcaaga[A/C]cagcctggccaacat | 55666 |
rs9915806 | snp | A/G | 0.256061 | 0.249927 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590551 | aggtcttactatgtt[A/G]cccaggctggtctct | 55666 |
rs9916546 | snp | C/T | 0.331411 | 0.236373 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563005 | tgtaatctcagcact[C/T]tgggaaccaaggcag | 55666 |
rs9916803 | snp | C/T | 0.330947 | 0.236533 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563106 | tttgagacagagtct[C/T]gctctgtcgcccagg | 55666 |
rs10445408 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562228 | cagggtgagattccg[C/T]ctcaaaacaaaacaa | 55666 |
rs10534151 | in-del | -/AA | 0.338523 | 0.233803 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599286 | AGAGCAAGACTCCTC[-/AA]AAAAAAAAAATAAAA | 55666 |
rs10588038 | snp | C/T | 0.405255 | 0.195948 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603014 | acacacacacacaca[C/T]atataaaagtcagac | 55666 |
rs10599354 | in-del | -/GTT | 0.48995 | 0.0701706 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595952 | GTTTTATGCTGTTAA[-/GTT]GTTCAGAATTTTTAC | 55666 |
rs10608622 | in-del | -/GCCG | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606214 | CTCTCTAAGGAGCCG[-/GCCG]TTTTCTCTAAGGGCA | 55666 |
rs10616542 | in-del | -/GCCG | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606210 | AATTCTCTCTAAGGA[-/GCCG]GCCGTTTTCTCTAAG | 55666 |
rs10627051 | in-del | -/AAA | 0 | 0 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635367 | AAAAAAAAAAAAAAA[-/AAA]GGAGTCGACGTTTCC | 55666 |
rs10652259 | in-del | -/TC | 0.365024 | 0.221967 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635926 | ACGAGGGACTGGTTT[-/TC]TCTGATTTGTCACTG | 55666 |
rs10695650 | in-del | -/TTAA | 0.495753 | 0.0466481 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606834 | AGAGAAGCAACTTAA[-/TTAA]ACATCACATTGGTGA | 55666 |
rs10871499 | snp | A/G | 0.459347 | 0.136653 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621980 | TCAAATCTGCTCAAT[A/G]GTAACTGCAGATTCA | 55666 |
rs11150795 | snp | C/T | 0.201418 | 0.245234 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557945 | TGGGGGGTAAGCCCA[C/T]GTGACCCACATTCTT | 55666 |
rs11150796 | snp | C/T | 0.330947 | 0.236533 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562100 | ttagccaggcgtggg[C/T]gcacgcctgtagtcc | 55666 |
rs11150797 | snp | A/G | 0.250732 | 0.249999 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562261 | CAACCCATGAGggcc[A/G]ggcgcggtggctcac | 55666 |
rs11150798 | snp | A/G | 0.332882 | 0.238955 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562289 | cacacctataatccc[A/G]gcactttgggaagcc | 55666 |
rs11150799 | snp | C/T | 0.128632 | 0.218563 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597739 | agtgtgccaggatcg[C/T]gccattgcactccag | 55666 |
rs11150800 | snp | C/T | 0.128288 | 0.218372 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597957 | aaaattagccgggcg[C/T]ggtggcgggtgcctg | 55666 |
rs11150801 | snp | A/C | 0.128288 | 0.218372 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598007 | ggctgaggcaggaga[A/C]tggtgtgaacccggg | 55666 |
rs11150802 | snp | A/T | 0.434109 | 0.169127 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605662 | caaaaaaaaaaaaaa[A/T]TGCTCTGCCCTTTAG | 55666 |
rs11303585 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568082 | GAGACTCTGTCTTCC[-/A]AAAAAAAAAAAAAAA | 55666 |
rs11335414 | in-del | -/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559748 | TTTTTTTTTTTTTTT[-/T]CTGAGGTAGGGTCTT | 55666 |
rs11375745 | in-del | -/T | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635974 | AGGAGTGTGTGACAA[-/T]TTTTTTTTTTTTTTT | 55666 |
rs11386487 | in-del | -/T | 0.330714 | 0.236612 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573485 | TGCTTGAAAATTAAA[-/T]TTCTGGCTGGTCCGA | 55666 |
rs11401963 | in-del | -/AA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611975 | AAAAAAAAAAAAAAA[-/AA]GAAAAGTGTTAAATA | 55666 |
rs11541221 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557476 | TTCCTCTCCCACTCG[C/T]TCGTCCTTATCCACC | 55666 |
rs11541222 | snp | C/T | 0.0923359 | 0.194016 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558082 | GGGGCCTGGCTCTTA[C/T]CCGGGGAGTGGTGGG | 55666 |
rs11541223 | snp | C/G | 0.195008 | 0.243947 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604611 | ATACGGACGGTACAC[C/G]GAGCACAAAGACATT | 55666 |
rs11541224 | snp | C/T | 0.373397 | 0.217424 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558983 | TGACAAGTCCCCCGC[C/T]GTGTTGGAAAGACCT | 55666 |
rs11541225 | snp | A/G | 0.163236 | 0.234461 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557877 | GAAGTGGTCAGGGCC[A/G]TGGCTGACACCTCCA | 55666 |
rs11650127 | snp | A/G | 0.262435 | 0.249691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605227 | tggagctcgcagtga[A/G]ctgagatggcgccac | 55666 |
rs11650460 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630179 | AGATGTTACTTTGGG[A/G]AAAAAAAAAAAAAAA | 55666 |
rs11651264 | snp | A/G | 0.45889 | 0.13735 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609368 | TGCCCAGGTTGGAGT[A/G]TGGTGGTGCAATCAT | 55666 |
rs11652797 | snp | A/G | 0.46014 | 0.13543 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607098 | CTATCACTAACATCC[A/G]AGAAAGCTTTCAAGA | 55666 |
rs11655346 | snp | A/G | 0.486332 | 0.08153 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605373 | AAAAACCagtcaggc[A/G]cggtggctcatgcct | 55666 |
rs11655377 | snp | A/T | 0.45889 | 0.13735 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605403 | tgtaatcccagcact[A/T]tgggaggtgaggcag | 55666 |
rs11656126 | snp | A/G | 0.261884 | 0.249717 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597516 | taggccgggtgcggt[A/G]gctcacgcctgtaat | 55666 |
rs11658312 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603749 | ATTCATTTTATTTTT[C/T]TATTGGATTTCAAGT | 55666 |
rs11867370 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587559 | tgaccttgtgatccg[C/G]ccgcctcagcctccg | 55666 |
rs11868361 | snp | A/G | 0.326035 | 0.238157 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584909 | cggtggctcacgcct[A/G]taatcctagcacttt | 55666 |
rs11868638 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558956 | CAATTCCAGGTGCCA[C/T]GTAGAGGCGAGAGGT | 55666 |
rs11869692 | snp | A/G/T | 0.0425829 | 0.139564 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626193 | agctggcacgtgcct[A/G/T]taatctcagttactc | 55666 |
rs11869693 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626209 | taatctcagttactc[G/T]ggaggctgagccagg | 55666 |
rs11869770 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625896 | gttcaagcctgtaat[C/T]ccaacactttgggag | 55666 |
rs11869779 | snp | C/T | 0.36315 | 0.222928 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603041 | agacatggtggtgca[C/T]gcctgtagtcccaga | 55666 |
rs11870789 | snp | A/C | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584995 | ggcaacatggtgaaa[A/C]cctgtctctactaaa | 55666 |
rs11870972 | snp | C/T | 0.139564 | 0.224285 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587843 | ccggcttattttttg[C/T]attttttttttttag | 55666 |
rs11871166 | snp | C/T | 0.139564 | 0.224285 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634310 | ccagccCAGAAACTT[C/T]TCAAAAGATCTCTTT | 55666 |
rs12185230 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624362 | ggcagaggttgcagt[A/G]agccaagatggcgcc | 55666 |
rs12325802 | snp | C/T | 0.441295 | 0.160954 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637882 | gaggttagaatgaac[C/T]gagttggtgccactg | 55666 |
rs12449763 | snp | A/T | 0.332799 | 0.23589 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560927 | gtgtaacggcttctc[A/T]tgttttaatttgcat | 55666 |
rs12449796 | snp | A/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561133 | tggctaatttttttt[A/T]tttttagtagagatg | 55666 |
rs12450110 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618390 | tctgcctggccgccc[C/G]gtctgagaagtgagg | 55666 |
rs12451074 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601924 | AAACTCTGAAAGCAG[C/T]TGCAGGGCACCCCAG | 55666 |
rs12451716 | snp | A/G | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596379 | ttgagaggtggaggc[A/G]ggaggtccacttgag | 55666 |
rs12453042 | snp | C/T | 0.168135 | 0.236216 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627766 | agagcgaaactctgt[C/T]tcaaaaaacaaaaac | 55666 |
rs12453887 | snp | A/G | 0.336245 | 0.234652 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556715 | AAGAAACTTATCGAG[A/G]AGCCAAGGTTGGGAG | 55666 |
rs12601028 | snp | C/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582990 | CCTGCGGCGCCGCCC[C/T]TGCGCACTCACAACT | 55666 |
rs12942146 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583922 | CTAGGTATAGATGCA[C/T]TTTTAATTTTGCTTT | 55666 |
rs12946371 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602904 | GTATATacacataca[C/T]acatatatatgtata | 55666 |
rs12946906 | snp | C/T | 0.486067 | 0.0822953 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632547 | TCGAACTCCTGACCT[C/T]AAGTTATCCACCCAC | 55666 |
rs12948099 | snp | C/G | 0.439641 | 0.162899 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633773 | GCGATGGCGCGACCT[C/G]GGTTCACTGCAACCT | 55666 |
rs12948353 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618545 | gaggtgaggggtcag[C/T]cccccgcccagccag | 55666 |
rs12948497 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560338 | gaatcccatgaaccc[A/G]ggaggggaagcctgc | 55666 |
rs12948708 | snp | A/G | 0.26271 | 0.249677 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591715 | TTGTGTAACCCTGCC[A/G]GAATGGCTGGCAGGA | 55666 |
rs12949956 | snp | C/T | 0.362104 | 0.223456 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575787 | TCACACTGAGTAAGA[C/T]TCTCCCACCTCCACC | 55666 |
rs12950353 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560224 | ggagtttgagaccag[C/T]ctggccaacatggcg | 55666 |
rs12953229 | snp | A/G | 0.262435 | 0.249691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587245 | tttggaggctgaggc[A/G]ggaggactgctcgag | 55666 |
rs17852305 | snp | C/G | 2.26411e-05 | 0.00336453 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559377 | GAGCCCCCGACGGCG[C/G]CGTACTCATGGAGAC | 55666 |
rs17852306 | snp | A/C | 0.0970261 | 0.197735 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613431 | GCCCGGTGGAACTGA[A/C]GTCTCCATTTCAGAT | 55666 |
rs17852307 | snp | A/C | 0.00857823 | 0.0649271 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81572047 | CTCCACAGGCAGGGG[A/C]CGGGCCAGCTGGGTG | 55666 |
rs28501531 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632250 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA | 55666 |
rs28521104 | snp | A/C | 0.251014 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600244 | CCGGAGAGAGCCAGT[A/C]CCCGACACAGCCCGG | 55666 |
rs28658175 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590189 | AGGTGCAGGTGCCAC[C/T]CCACGGCCGTGGGCA | 55666 |
rs28660208 | snp | C/T | 0.441158 | 0.161117 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637468 | TTTTTTTTTTAAGTA[C/T]TTTTTAAATTTAACA | 55666 |
rs34004934 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630809 | TAAACCAGGGAGGTC[-/C]GAGGCTACAGTGAGC | 55666 |
rs34045634 | in-del | -/C | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562688 | CATGGTGGCTTACCA[-/C]CTGCAATCTCAGCAC | 55666 |
rs34070114 | snp | A/G | 0.00121207 | 0.0245879 | synonymous-codon, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81589061 | TGCCATACACTGATT[A/G]GACACCTGGTACCCT | 55666 |
rs34091682 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583625 | CCCATATGCTTTCCT[-/A]AAAAACTACACGTGA | 55666 |
rs34164306 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592821 | AAACCCCGTCTCTAC[-/A]AAAAATACAAAAATT | 55666 |
rs34176297 | in-del | -/A | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619568 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAAGAAAAG | 55666 |
rs34194298 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602054 | AAACAAAGAAGGGGG[-/G]ATAGTATGAATGTGC | 55666 |
rs34211449 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576414 | GGAAACTCATGTATA[-/C]CGGAGGTCTAACTTT | 55666 |
rs34386430 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634590 | ACCAATGATTAACAC[-/T]TTTTTTTTTTTTTTT | 55666 |
rs34450012 | in-del | -/A | 0.335101 | 0.23507 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560697 | AACAAACAAACAAAC[-/A]AACAACAACAACAAA | 55666 |
rs34488489 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576227 | TGGATTATGGATCTC[-/A]AAAATAAAATTAAAT | 55666 |
rs34491624 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620609 | TGCAATGGTGACACA[-/T]TAAGGTTCATCCATC | 55666 |
rs34537710 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600945 | TTACAGGGACACTAT[A/G]AACTCCACAGAGAGC | 55666 |
rs34558194 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584570 | TCATGAGTGCTGTTT[-/G]GGGAGATCCCAGGCA | 55666 |
rs34614358 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576938 | GTGGGAGGACACACA[-/G]GACCCTTCGAGTACA | 55666 |
rs34635363 | snp | A/G | 0.262985 | 0.249663 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582224 | ACAACCAGGAGGGCC[A/G]TGAGGTAAGCGAGCT | 55666 |
rs34643456 | in-del | -/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587674 | CAAAGAAAAAAGTTG[-/T]TTTTTTTTTTTTTTT | 55666 |
rs34705837 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617318 | TTGCTCTGTTGCCCA[A/G]CTGCAGTGCAGTGGC | 55666 |
rs34722507 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603022 | ACACACATATATAAA[-/A]GTCAGACATGGTGGT | 55666 |
rs34746217 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585661 | GAAGACTCCATTTCT[-/G]GGGGGGGGGGGGAAA | 55666 |
rs34749567 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619572 | AAAAAAAAAAAAGAA[A/G]GAAAAGAAAAGAAAA | 55666 |
rs34755486 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559748 | TTTTTTTTTTTTTTT[-/T]CTGAGGTAGGGTCTT | 55666 |
rs34792466 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588325 | AATTGGCAGGATTCT[-/A]AAAAAGGTCCCGAAA | 55666 |
rs34799675 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569907 | CAGACACCCCTCCCC[-/C]AAAGCAGCACCGAGT | 55666 |
rs34876059 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572942 | CCCACACCAATCTGT[-/C]CAAAGTCTCAACTTG | 55666 |
rs34905643 | in-del | -/TT/TTT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628898 | CTTTTTTTTTTTTTT[-/TT/TTT]GAGACAGTCTCACTC | 55666 |
rs34936180 | in-del | -/TC | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635927 | CGAGGGACTGGTTTT[-/TC]CTGATTTGTCACTGA | 55666 |
rs35010915 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569355 | TCCGGCCTGTGCACC[A/G]GCCTCGACGTCGGAC | 55666 |
rs35078498 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591240 | GGAGTTCAAGACCAG[-/C]CCTGGAAAACATGGT | 55666 |
rs35083561 | in-del | -/TTAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606835 | AGAAGAGAAGCAACT[-/TTAA]TAAACATCACATTGG | 55666 |
rs35107551 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568603 | AACACGGGAGCCACG[C/T]TAAGCAGCAGATCAA | 55666 |
rs35302133 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600977 | ATGAGCTCACCAACC[-/C]TAAGGAAGGGAAAAG | 55666 |
rs35337296 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595428 | GACAGTAAGACTGTC[-/A]AAAAAAAAAAAAAAA | 55666 |
rs35340912 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619218 | CAAGAATGATCAATT[-/A]AAAAAAAAAAAAAAA | 55666 |
rs35394558 | in-del | -/T | 0.375 | 0.216506 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633873 | TTTTTTTTTTTTTTT[-/T]AAGAGTCTCACTCTG | 55666 |
rs35396713 | in-del | -/A | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612734 | AAATCTAAAATAAAC[-/A]AATGTACATATGCAT | 55666 |
rs35435780 | snp | G/T | 0.45889 | 0.13735 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612576 | TGGAATCCCAATACC[G/T]CAAAGTCAGCACCCC | 55666 |
rs35473939 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585171 | CGAGACTCTGTCGCC[-/A]AAAAAAAAAAAAAAA | 55666 |
rs35496389 | snp | G/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574126 | CAAAAATACAGGCTT[G/T]CCCCTACAAGAAATA | 55666 |
rs35511117 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81629730 | CCACAGATACCTTTT[-/T]CAAAAATGTTGCTGC | 55666 |
rs35522582 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576246 | ATAAAATTAAATCCT[-/A]AAAGCACGGAAAGAG | 55666 |
rs35549457 | in-del | -/A | 0.375 | 0.216506 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634448 | GTGGGAAAAAAAAAA[-/A]TGGCCTTGTCTGAAA | 55666 |
rs35549981 | in-del | -/AATA/AATT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606836 | GAAGAGAAGCAACTT[-/AATA/AATT]AAACATCACATTGGT | 55666 |
rs35650543 | in-del | -/G | 0.488666 | 0.0744214 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626918 | ACATAGTGAAACCTC[-/G]GTCTCTACTAAAAAT | 55666 |
rs35677141 | in-del | -/A | 0.276534 | 0.248588 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594777 | ACTCCGTCTCTAGGG[-/A]AAAAAAAAAAAATTA | 55666 |
rs35704372 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598627 | TGACCCAGCAACCCC[-/C]TGCACGTTCAGTGTA | 55666 |
rs35734855 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585698 | ATCAGAGGCTGGGTG[-/C]CAGTGGCTCACATCT | 55666 |
rs35787010 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595120 | GGCTGGTCTCAAACT[-/A]CCCAGTCTCAAGGGA | 55666 |
rs35816741 | snp | G/T | 0.421842 | 0.181577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582575 | CCCGACTAATTTTTT[G/T]TTGTTGTTGTAGAAA | 55666 |
rs35868252 | snp | C/G | 0.45889 | 0.13735 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608446 | CCAGGCGAGGTGGCT[C/G]ACACCTGTAATCCAG | 55666 |
rs35868511 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590566 | CCCAGGCTGGTCTCT[-/A]AACTCCTGGCCCCAT | 55666 |
rs35879038 | in-del | -/T/TA | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603019 | ACACACACACATATA[-/T/TA]AAAAGTCAGACATGG | 55666 |
rs35880908 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597218 | CCAAGCCATAGGGCC[-/A]CACGCACAGTCCTGT | 55666 |
rs35887231 | snp | A/G | 0.363359 | 0.222822 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620100 | AATTTCAAGAAAAGG[A/G]AAGAGATGGAAGGGG | 55666 |
rs35897480 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593882 | CAGGGTGCCCTAACA[-/G]GGTTCTGTAATGCAG | 55666 |
rs35939173 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630097 | ATGTAAAACACTTTT[-/T]GTCTCTTCAGACTTA | 55666 |
rs36000667 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583859 | ATCCATGTGCAAATG[-/C]CCTATACGTGTCTTC | 55666 |
rs36004502 | in-del | -/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566950 | TGCCAACTGTGCAGC[-/G]TGTGAGCTTGGGGTC | 55666 |
rs36038099 | in-del | -/G | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556475 | AAGCAGGAACACAGG[-/G]CAGTGTGTCACCCCC | 55666 |
rs36068179 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571062 | CTTAATTACACCCTA[-/G]GTAGTCTAAAAACCA | 55666 |
rs36090666 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631062 | CTGTAATCCCAGCTA[-/A]CCCGGGAGGCTGAGG | 55666 |
rs36112637 | snp | C/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569812 | GAGGGCACTTTGCAC[C/T]TAAGATATAATCAAT | 55666 |
rs55730623 | snp | A/G | 0.261728 | 0.249725 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567567 | ACATGAATGTTCCAT[A/G]CAGTTCCCCAGTGCC | 55666 |
rs55784792 | snp | C/G | 0.0566069 | 0.158427 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558474 | AGGGAGAACTGACTG[C/G]TGCCCCCGTCCACAC | 55666 |
rs55849409 | in-del | -/AA/AAA | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637949 | AAAAAAAAAAAAAAA[-/AA/AAA]GACGTCACTTCACAG | 55666 |
rs55857349 | in-del | -/A | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626319 | AAGAAAAAAAAAAAA[-/A]GAAAAGAATGAAAAT | 55666 |
rs55885844 | in-del | -/AATTA | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638086 | TACATTAATTGATTA[-/AATTA]TGTTAGTAATTGTAT | 55666 |
rs55908909 | snp | C/T | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556662 | CGGGGCCGTCAAACA[C/T]TGACGCACTCTCCTC | 55666 |
rs56050665 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631440 | TATATATATATATTT[A/T]TTTTTTTTTTTTTTT | 55666 |
rs56064069 | snp | A/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631438 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 55666 |
rs56118967 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631457 | TTTTTTTTTTTTTTT[C/T]TTTTTCCCCCACGGC | 55666 |
rs56146108 | in-del | -/T | 0.486133 | 0.082104 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638049 | TGTGACAGTTTTTTT[-/T]AAACTATGTTAAATT | 55666 |
rs56167198 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611538 | TATTTTTAGTAGAGA[C/T]GGGATTTCACCATAT | 55666 |
rs56216280 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573996 | TGGCTGTGATGGGGG[C/T]GCTAAAGACACAGGG | 55666 |
rs56232837 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631460 | TTTTTTTTTTTTTTT[C/T]TTCCCCCACGGCAAG | 55666 |
rs56233095 | in-del | -/AAA | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613137 | GCTAAAAAAAAAAAA[-/AAA]CAAAAACCGATAAAA | 55666 |
rs56263206 | snp | A/G | 0.256619 | 0.249912 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575603 | TGAACCTCCTAAAGC[A/G]ATCGGCAAGGACAGC | 55666 |
rs56368424 | in-del | -/TTCTGCTTGTCTCTGAAGCTACTGACGT | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614571 | GTCAGACTTAAGGGT[-/TTCTGCTTGTCTCTGAAGCTACTGACGT]ACTGCTTTCCAAAAA | 55666 |
rs56770353 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626982 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAA | 55666 |
rs56778656 | snp | C/G | 0 | 0 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635310 | CACCACTGAACTCCA[C/G]CCTGGGCGACAGAGT | 55666 |
rs56835867 | snp | C/T | 0.158302 | 0.232576 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633815 | GTTCAAGCAATTCTC[C/T]TGCCTCAAGCCTCCC | 55666 |
rs56999682 | in-del | -/AC/CA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576002 | TGCCAGCAAATACAA[-/AC/CA]GTGGGTTACAGGGCT | 55666 |
rs57081004 | in-del | -/TA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602933 | ACACATATATATATA[-/TA]CACACACATATATAT | 55666 |
rs57135500 | snp | A/G | 0.204496 | 0.245824 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612720 | AAAAGGAATTGCAAA[A/G]AATCTAAAATAAACA | 55666 |
rs57146509 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634040 | GTATTTTTTTTTTTT[-/T]AGTAGACGTGGGGTT | 55666 |
rs57186605 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612679 | ATGGCCAAGTATAAA[C/T]TCAGATCCTTCTCAC | 55666 |
rs57187961 | in-del | -/TTCT | 0 | 0 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567219 | TGAAAAAATTAATCT[-/TTCT]ATCAACAAGCTTCTT | 55666 |
rs57190405 | in-del | -/AA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633143 | AAAAAAAAAAAAAAA[-/AA]AGAAAAGAAATACAA | 55666 |
rs57196616 | in-del | -/GCG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576650 | AAGAACGAAAACCTG[-/GCG]TGTGTTTGCAACACA | 55666 |
rs57463122 | in-del | -/TTTTT | 0.46939 | 0.119868 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637452 | GATCACACCTTCATG[-/TTTTT]TTTTTTAAGTATTTT | 55666 |
rs57514828 | snp | C/T | 0.206642 | 0.246211 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624274 | AATACAAAAATTAGC[C/T]AGGCGTGGTGGCGGA | 55666 |
rs57607963 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585673 | TTCTGGGGGGGGGGG[-/G]AAAGAAAGAAATCAG | 55666 |
rs57639613 | in-del | -/AAAAAAAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587647 | AAAAAAAAAAAAAAA[-/AAAAAAAA]GGAAAAAAGAAACAA | 55666 |
rs57660144 | snp | A/G | 0.158302 | 0.232576 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631320 | GAGACCAAGGCAGGA[A/G]GATCTCTTTAGCCTA | 55666 |
rs57856422 | snp | A/G | 0.491987 | 0.0627894 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585078 | GGGAGGCTGAGGCAG[A/G]AGAATTGCTTGAACC | 55666 |
rs58274256 | snp | C/T | 0.206642 | 0.246211 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607339 | TCAATGAGAAAATCC[C/T]GGACCCTACTCTGAA | 55666 |
rs58346580 | in-del | -/T | 0.355311 | 0.226737 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632329 | TTCCTTTTTTATTTC[-/T]TTTTTTTTTTTCAGC | 55666 |
rs58398000 | snp | A/G | 0.4862 | 0.0819127 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609897 | AATGATAAGCACGGA[A/G]GCCGACAGGCTCAGC | 55666 |
rs58774657 | in-del | -/CACACACACACA | 0 | 0 | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81564117 | ACACACACACACACA[-/CACACACACACA]AAGAGCAGGGCGGGC | 55666 |
rs58789368 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616963 | GGCACCAAAGTCAGT[A/G]GCTCTTCCCAAATCT | 55666 |
rs58976732 | snp | C/G | 0.164219 | 0.234823 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602350 | CCAGGAGTTTGAGAC[C/G]AGCGTGGGCCACACA | 55666 |
rs59468852 | snp | A/G | 0.25634 | 0.24992 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587455 | CGAGTAGCTGGAACT[A/G]CAGGCGCCTGCCACC | 55666 |
rs59714954 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580140 | CTCAGCCATCCCCTC[A/C]AGGATGGACAACTCG | 55666 |
rs59874864 | snp | A/G | 0.157972 | 0.232445 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635711 | CGCGCCGGGCCTGGA[A/G]ACCTATTCTAGACAA | 55666 |
rs60044674 | in-del | -/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605293 | CTCAAAAAAAAAAAA[-/T]AAATAATAATAATAA | 55666 |
rs60052576 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589491 | TGCAGTGAGCCGAGA[C/T]TGTGCCGCTGCACTC | 55666 |
rs60092546 | in-del | -/A/AA | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623484 | AAAAAAAAAAAAAAA[-/A/AA]GCAAAACTCTGTCTC | 55666 |
rs60179545 | snp | C/T | 0.0271762 | 0.113356 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558744 | CGTGTCCAGGGCCAC[C/T]GCGTCCCCACCAGAC | 55666 |
rs60365534 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604290 | CCTGGACACAGCAGA[C/T]GAGATAAAAACACTG | 55666 |
rs60450259 | snp | A/G | 0.363985 | 0.222503 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634830 | CCTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 55666 |
rs60716083 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637452 | GATCACACCTTCATG[-/T]TTTTTTTTTTAAGTA | 55666 |
rs60735748 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625463 | AGGAATGTGAATCTC[A/G]GTAAAGAAACAAATC | 55666 |
rs60976339 | in-del | -/AGA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570943 | TTCCTTTATAAAAGA[-/AGA]GGAAAGAAGTGGGGA | 55666 |
rs61177234 | snp | C/G | 0.155987 | 0.23165 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613612 | AGGCCTAAACAATGA[C/G]GTTTCTAACTTTTAA | 55666 |
rs61207557 | snp | A/G | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587477 | CCTGCCACCATGCCC[A/G]GCTAACTTTTTGTAG | 55666 |
rs61252917 | snp | A/C | 0.154993 | 0.231244 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637485 | TTTTAAATTTAACAT[A/C]AGAAAAACAAACGAG | 55666 |
rs61419766 | in-del | -/CA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574896 | CACACACACACACAC[-/CA]ACACAAACACAAAAG | 55666 |
rs61456370 | snp | A/C | 0.204496 | 0.245824 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613038 | GTGTGAGGCCCCCAA[A/C]TCCCCCAATACCTTT | 55666 |
rs61459862 | in-del | -/A | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595443 | AAAAAAAAAAAAAAA[-/A]CCCGTTTTGCTTTTT | 55666 |
rs61478620 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623447 | TCCAGCCTGGGTGAC[A/G]GAGCAAGACTTTGTT | 55666 |
rs61586425 | snp | A/C | 0.489201 | 0.0726845 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623809 | TCTCAAAAAAAAAAA[A/C]AAAACTCAATTCCAA | 55666 |
rs61744362 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614741 | GCTGACCTCAGAGGC[A/T]AACAAGCATCTCCAC | 55666 |
rs61746623 | snp | C/T | 0.0498117 | 0.149749 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614622 | CCAAAAAGGTTGCCA[C/T]AAGTCACATCTGGTT | 55666 |
rs62073394 | snp | C/T | 0.106278 | 0.204558 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562161 | CACTTGAACCCAGGA[C/T]GTGGAGGTTGCAGTA | 55666 |
rs62073395 | snp | G/T | 0.303007 | 0.244316 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563941 | GATGGCAACGCCAGG[G/T]GTGGTGGTACACATC | 55666 |
rs62073396 | snp | A/G | 0.104149 | 0.203046 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566919 | CCCTCTTCTCCCCCA[A/G]CGGTGTCTCTTAAAA | 55666 |
rs62073398 | snp | A/G | 0.115788 | 0.21092 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568249 | TTCTCCATCTAGGGC[A/G]GCAAGAGGGAGGAAT | 55666 |
rs62073399 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568335 | TTCAAGAGTGCACCC[C/T]AATAACTGGCTTTGC | 55666 |
rs62073400 | snp | A/G | 0.257454 | 0.249889 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569200 | CATCTCCCAGAGCCC[A/G]AATTAACGACTCCTA | 55666 |
rs62073401 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569302 | ACACTTGGAAACTCC[A/G]CCATCCTGGAGACAA | 55666 |
rs62073402 | snp | C/T | 0.106987 | 0.205054 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569912 | CACCCCTCCCCAAAG[C/T]AGCACCGAGTTGAGT | 55666 |
rs62073403 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570575 | ACAGCCCATCCCAGA[C/T]GTCCCAAGGAAGGGC | 55666 |
rs62073404 | snp | A/G | 0.106987 | 0.205054 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571276 | AATGAGCCGCCTCCC[A/G]TCCGCTTTGGACAGA | 55666 |
rs62073405 | snp | A/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573485 | TTGCTTGAAAATTAA[A/T]TTCTGGCTGGTCCGA | 55666 |
rs62073406 | snp | A/G | 0.084728 | 0.187577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574357 | ACTCCCCAAGAAAAT[A/G]AAGGTGTTGTATCCC | 55666 |
rs62073407 | snp | A/C | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574898 | ACACACACACACACA[A/C]ACAAACACAAAAGCA | 55666 |
rs62073408 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575095 | CAAAGCTTTCAGACA[C/T]TCGGTTACTTTTCTT | 55666 |
rs62073409 | snp | A/G | 0.107694 | 0.205546 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575580 | ACAGGAAGGGTTACA[A/G]AGATGAGTGAACCTC | 55666 |
rs62073410 | snp | A/G | 0.107694 | 0.205546 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576021 | GGTTACAGGGCTATA[A/G]CAAACAGAGCAGTTT | 55666 |
rs62073411 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576318 | TGGCCGTTGCACAAC[A/G]CGGGTTTGAACTGAG | 55666 |
rs62073412 | snp | A/G | 0.105214 | 0.203807 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578175 | CAGAACTCACTTTCC[A/G]TAAGTCTTTCCATGG | 55666 |
rs62073413 | snp | C/T | 0.105214 | 0.203807 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578975 | GCCCAGGCAGGAGTG[C/T]AGTGGTGCAATCAAA | 55666 |
rs62073414 | snp | C/G | 0.105214 | 0.203807 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579683 | CATGCCCCTTCCTCT[C/G]TGTGTGCCAATTAGC | 55666 |
rs62073415 | snp | A/G | 0.327914 | 0.237549 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580088 | CAGCTCCTGCCTCCC[A/G]GTGCTCTCCACCTCA | 55666 |
rs62073416 | snp | G/T | 0.0850919 | 0.187897 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580693 | TACCCGTTCCGCTGG[G/T]GTGGCCCACCTCCCC | 55666 |
rs62074662 | snp | G/T | 0.10237 | 0.201756 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583483 | GCAGGGGACAAATGT[G/T]CCCTTTCACAAGAAA | 55666 |
rs62074663 | snp | A/T | 0.10237 | 0.201756 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583830 | ATGTGTGAGTGCATG[A/T]AAATGTATGTCCACA | 55666 |
rs62074665 | snp | C/T | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587221 | GCTCACGCCTATAAC[C/T]CCAACACTTTTGGAG | 55666 |
rs62074666 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589358 | ACACGGTGAAACCCC[A/G]TCCCTACTAAAAATA | 55666 |
rs62074667 | snp | C/T | 0.104859 | 0.203554 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591058 | ATGACACTGAAAGAA[C/T]GCAGGGCTCAGAGGG | 55666 |
rs62074668 | snp | C/G | 0.0850919 | 0.187897 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595090 | TTGTAGAGATGGGGA[C/G]TTGCCATGTTGCCCA | 55666 |
rs62074669 | snp | C/T | 0.10237 | 0.201756 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595689 | AGCTGGGATTACAGG[C/T]GCCCACCACCATGCC | 55666 |
rs62074670 | snp | C/G | 0.16911 | 0.236552 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597173 | GCGGTGCAAAGAGAC[C/G]CTGATAATGCAGGCC | 55666 |
rs62074671 | snp | G/T | 0.155019 | 0.231255 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81597278 | GACGGTACCCTTTCG[G/T]GTATCTTCTGAGACG | 55666 |
rs62074672 | snp | C/G | 0.10237 | 0.201756 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597612 | CAACATGGAGAAACC[C/G]TGTCTCTACTAAAAA | 55666 |
rs62074673 | snp | C/T | 0.10237 | 0.201756 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599975 | AAGGGAGAGCTCAGG[C/T]AGAAGGGACACACAT | 55666 |
rs62074674 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602984 | ATACACAAATACACA[A/C]ACACACACACACACA | 55666 |
rs62074675 | snp | C/T | 0.246769 | 0.249979 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603012 | ACACACACACACACA[C/T]ACATATAAAAGTCAG | 55666 |
rs62074676 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603018 | ACACACACACACATA[A/T]AAAAGTCAGACATGG | 55666 |
rs62074677 | snp | C/T | 0.158518 | 0.232661 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606858 | CACATTGGTGAAAAG[C/T]TGAGCAAGAGGCTGG | 55666 |
rs62074679 | snp | A/G | 0.113685 | 0.209567 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612155 | TCACAGAAGCCTTGG[A/G]AGCACAACACGCACA | 55666 |
rs62074680 | snp | A/C | 0.169435 | 0.236663 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613700 | TGCAGGTTCTCTGTA[A/C]TTTAATCTCTTACAA | 55666 |
rs62074725 | snp | C/G | 0.101301 | 0.200969 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617794 | CTGCCGAGTGCCTGC[C/G]ATTGCAGGCGCGCGC | 55666 |
rs62074726 | snp | A/G | 0.127944 | 0.218179 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617811 | TTGCAGGCGCGCGCC[A/G]CCACGCCTGACTGGT | 55666 |
rs62074729 | snp | C/G | 0.102014 | 0.201495 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621383 | AACCAGCCCATCATT[C/G]TGGCTGGTAAACAGG | 55666 |
rs62074730 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623396 | CTTGGGCCTGGGAGG[C/T]AGAGGCTGCAGTGAG | 55666 |
rs62074731 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623402 | CCTGGGAGGTAGAGG[C/T]TGCAGTGAGTCGAGA | 55666 |
rs62074732 | snp | A/G | 0.126909 | 0.217598 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624647 | GCTGTCAAGCAGTTT[A/G]CCAACAAATGGGGGA | 55666 |
rs62074733 | snp | A/G | 0.126564 | 0.217402 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624724 | AAGAAACCTCAGATG[A/G]GAGGCTAGAAGTCTC | 55666 |
rs62074734 | snp | A/G | 0.178465 | 0.239547 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625924 | GAGGCCGAGTTGGGC[A/G]GATCACCTGAAGTCA | 55666 |
rs62074735 | snp | A/G | 0.10237 | 0.201756 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627971 | AATGAAAATATCCTT[A/G]GGAGGCCAAGGCGGG | 55666 |
rs62074736 | snp | A/G | 0.177824 | 0.239355 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628373 | CAAAAAATTAGTCAG[A/G]TATGGTGGCGGGTGC | 55666 |
rs62074737 | snp | C/T | 0.168785 | 0.236441 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628536 | AGAAAATAACCCTCA[C/T]ATAAACACAGGGCAA | 55666 |
rs62074738 | snp | A/G | 0.164873 | 0.23506 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630667 | CGGTGGATCACTTGA[A/G]CTCAGAAGTTCAAGA | 55666 |
rs62074739 | snp | C/G | 0.164873 | 0.23506 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631861 | CTGGAGTACAATGGC[C/G]CAATCTTGGCTCACT | 55666 |
rs62074740 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632369 | CCAGGCTGGAGTGCA[A/G]TGGCGTGATCTCGGC | 55666 |
rs62074741 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632374 | CTGGAGTGCAATGGC[A/G]TGATCTCGGCTCACT | 55666 |
rs62074742 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632383 | AATGGCGTGATCTCG[A/G]CTCACTGCAACCTCT | 55666 |
rs62074743 | snp | A/C/T | 0.0584853 | 0.160693 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632406 | CAACCTCTGCCTCCC[A/C/T]GGTTCAAGTGATTCT | 55666 |
rs62074744 | snp | A/G | 0.10237 | 0.201756 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634253 | TTATTCACCTGCCTC[A/G]GCCTCTCAAAGTGCT | 55666 |
rs62074745 | snp | A/C | 0.15698 | 0.23205 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634563 | ATTCCTAACCTATTT[A/C]TAGGCAAAGTCACCA | 55666 |
rs62074746 | snp | G/T | 0.15665 | 0.231917 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635148 | AGTTCGAGATCAACC[G/T]GGCCAACACGGTGAA | 55666 |
rs62074747 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635325 | GCCTGGGCGACAGAG[C/T]GAGACTCCATCTCAA | 55666 |
rs62074748 | snp | A/T | 0.1652 | 0.235179 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635963 | TTTACGTTAAGGAGG[A/T]GTGTGTGACAATTTT | 55666 |
rs62074749 | snp | A/G | 0.0962929 | 0.197165 | upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637159 | GTTCCGGCCCCACCA[A/G]CGGCTCGACGCATGC | 55666 |
rs62074750 | snp | A/T | 0.164219 | 0.234823 | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637238 | GGGGATTTTGGAAAG[A/T]TGCGTCTGAGATTAC | 55666 |
rs67050149 | snp | A/C | 0.264906 | 0.249555 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590017 | AAATTCATCTGGAGG[A/C]AGAGAGATGGGGAAG | 55666 |
rs68054435 | in-del | -/CA/GT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605818 | GGCAAAAAACAAACA[-/CA/GT]TTTTCTTTTTTTTTT | 55666 |
rs70938164 | multinucleotide-polymorphism | CCC/TTT | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631454 | TATTTTTTTTTTTTT[CCC/TTT]CCCCCACGGCAAGCC | 55666 |
rs71166157 | in-del | -/AA/CA/CAAA | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574901 | ACACACACACACACA[-/AA/CA/CAAA]AACACAAAAGCATGT | 55666 |
rs71166160 | in-del | -/AAA | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616741 | TCTCAAAAAAAAAAA[-/AAA]GAGTAACACACTACC | 55666 |
rs71354604 | multinucleotide-polymorphism | CGGGAAGCGGAGCTTGCAGTGAGCCGAGATT/GGGGGGACGCAGCTGGCAGTGAGCGGACGTC | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610876 | AGAATGGCGTGAACC[lengthTooLong]GCGCCACTGCACTCC | 55666 |
rs71354605 | in-del | CTCCAGCCTGGGT/GTCCGCAGTCCGGCCTGGGC | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611926 | CGTCGCGCCACTGCA[lengthTooLong]GACAGAGCGAGAGTC | 55666 |
rs71354606 | multinucleotide-polymorphism | CTCCG/GTCCA | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611951 | GGTGACAGAGCGAGA[CTCCG/GTCCA]TCTCAAAAAAAAAAA | 55666 |
rs71354607 | in-del | AAACAAAAACT/CAAAAACC | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613140 | GCTAAAAAAAAAAAA[AAACAAAAACT/CAAAAACC]GATAAAAAGCTAACA | 55666 |
rs71367065 | in-del | -/AC | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574876 | CAAACAAACAAACAA[-/AC]ACACACACACACACA | 55666 |
rs71367066 | in-del | -/GTC | 0.484066 | 0.0878235 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581375 | AAAAAAAAAAAAAAA[-/GTC]AGTTAATAAAATCAC | 55666 |
rs71367067 | in-del | -/AAAA | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591472 | AAAAAAAAAAAAAAA[-/AAAA]CCTGCTCTGGTGTTT | 55666 |
rs71367068 | in-del | -/A | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598095 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55666 |
rs71367069 | multinucleotide-polymorphism | CA/TG | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610734 | GAGGCGGGTGGATCA[CA/TG]AGGTCAGGAGATCGA | 55666 |
rs71367071 | in-del | -/A | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623464 | GCAAGACTTTGTTTC[-/A]AAAAAAAAAAAAAAA | 55666 |
rs71367073 | in-del | -/AA | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633127 | GCAAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 55666 |
rs71370216 | snp | A/G | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585195 | AAAAAAAAAAAAAAA[A/G]GAGTTTGGTATTAGT | 55666 |
rs71373084 | snp | C/G | 0.261884 | 0.249717 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597904 | TCAAGACCATCCTGG[C/G]TAACATGGTGAAATC | 55666 |
rs71373085 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601152 | TTAAATGTAGCTTGC[A/G]GGTCATTCAAAGGTA | 55666 |
rs71373086 | snp | A/C/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610748 | ATGAGGTCAGGAGAT[A/C/T]GAGACCATCCTGGCT | 55666 |
rs71373087 | snp | A/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610763 | CGAGACCATCCTGGC[A/T]AACAAGGTGAAACCC | 55666 |
rs71373088 | snp | A/C | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610768 | CCATCCTGGCTAACA[A/C]GGTGAAACCCCGTCT | 55666 |
rs71373089 | snp | C/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610784 | GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 55666 |
rs71373090 | snp | A/G | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610809 | TACAAAAAATTAGCC[A/G]GGCGCGGTGGCGGGC | 55666 |
rs71373091 | snp | C/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610814 | AAAATTAGCCGGGCG[C/T]GGTGGCGGGCGCCTG | 55666 |
rs71373092 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610844 | GTAGTCCCAGCTACT[A/C/T]GGGAGGCTGAGGCAG | 55666 |
rs71373093 | snp | A/G | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611977 | AAAAAAAAAAAAAAA[A/G]AAAAGTGTTAAATAA | 55666 |
rs71373096 | snp | A/C | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624891 | CAGAGGCCAATAAAC[A/C]ATAAGGAAGATGGAA | 55666 |
rs71694803 | in-del | -/TT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628885 | TCTACAATTCATACT[-/TT]TTTTTTTTTTTTTGA | 55666 |
rs71866573 | in-del | -/T | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635975 | GGAGTGTGTGACAAT[-/T]TTTTTTTTTTTTTTT | 55666 |
rs71924317 | in-del | -/AC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574877 | CAAACACACACACAC[-/AC]ACACACACACAAACA | 55666 |
rs72032041 | in-del | -/AC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603005 | ACACACACACACACA[-/AC]CACACACACATATAA | 55666 |
rs72062777 | in-del | -/TTC | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615101 | GAGACGTCTGTTTCT[-/TTC]TTTTTTTTTTTTTTT | 55666 |
rs72532153 | in-del | -/CT | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635928 | GAGGGACTGGTTTTC[-/CT]TSWTTTGTCACTGAT | 55666 |
rs72855621 | snp | C/G | 0.251859 | 0.249993 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562528 | TGGGCAACAGAACAA[C/G]ACTTTGTCTCAAAAC | 55666 |
rs72855624 | snp | A/G | 0.259397 | 0.249823 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562724 | CGGGAGGATCGCTTG[A/G]GCCCAAGAGTTCAAG | 55666 |
rs72855627 | snp | G/T | 0.327914 | 0.237549 | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81564157 | TATTAGGTACTATGT[G/T]TAGTACCTGGGTGAT | 55666 |
rs72855648 | snp | A/T | 0.249603 | 0.25 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572172 | TTGTCTCACCTTTTA[A/T]TTAATTAATTTATTT | 55666 |
rs72855653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572535 | TGAAGTGTATGGATA[A/G]CAGAAAGGAAAACGT | 55666 |
rs72855663 | snp | C/G | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579519 | TCCACTCCAGCCTCC[C/G]CCTTCAGCTGACCCT | 55666 |
rs72855665 | snp | A/G | 0.25634 | 0.24992 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581409 | GTCACAAAAGAACTG[A/G]AAGCCAGCCCCTTGT | 55666 |
rs72855675 | snp | A/C | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585269 | TAACATCCATGATTC[A/C]TGGAGATGACCGACG | 55666 |
rs72855689 | snp | A/T | 0.267636 | 0.249377 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594323 | ACTCAACTAATTCAC[A/T]TGTAAAATAGTTAAC | 55666 |
rs73369234 | snp | C/G | 0.155987 | 0.23165 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572710 | CCTGGCACTCAGGCG[C/G]GATCTGCGACAGGCA | 55666 |
rs73369240 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582749 | AGACAGTCAAGCGCC[C/T]CCTGGCTGTACAACA | 55666 |
rs73369254 | snp | A/G | 0.153997 | 0.230832 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595019 | AAGTGCAAAAACTTC[A/G]CAGTCAGCTTGAACA | 55666 |
rs73369283 | snp | C/T | 0.204189 | 0.245767 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621316 | AATGCTACAATTGCA[C/T]GTTGTGTCCCTAGAC | 55666 |
rs73369285 | snp | C/T | 0.155987 | 0.23165 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621573 | CCAGCACCCGTGTTC[C/T]GTAAAGGACCAGTCA | 55666 |
rs73369286 | snp | C/T | 0.204803 | 0.245881 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622006 | ATTCAGGATAATTAC[C/T]GAATTCCTGGCAAGC | 55666 |
rs73369290 | snp | A/G | 0.206336 | 0.246157 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623124 | ACTTGAAGCTGGGAG[A/G]CAGAGGTTGCAGGGA | 55666 |
rs73369296 | snp | A/G | 0.158302 | 0.232576 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631390 | TCCTAATTTAATAAC[A/G]TGTGTGTGCATATAT | 55666 |
rs73369300 | snp | C/G | 0.158302 | 0.232576 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632267 | GGCATGAGCCACCAA[C/G]CCTGGCCTAGCTGAT | 55666 |
rs73369302 | snp | A/G | 0.158302 | 0.232576 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632647 | ATAAATTCTATAACT[A/G]TTTTCTGTGAGGTTA | 55666 |
rs73371204 | snp | C/T | 0.155987 | 0.23165 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633716 | CAGAAACTCTTTTCT[C/T]CCCCCAAGACAGAGT | 55666 |
rs73371205 | snp | A/G | 0.158302 | 0.232576 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635002 | CAGAGACCAGCCTGT[A/G]CAACATAGTAGAGAC | 55666 |
rs73371206 | snp | A/C | 0.158302 | 0.232576 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635192 | TAAAAATAAAAAAGA[A/C]ATCAGCCATGCGTGT | 55666 |
rs74002427 | snp | C/T | 0.0193772 | 0.0965046 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557711 | GCTGGGAGTTGCATC[C/T]GCAGCAGTCCGCTTC | 55666 |
rs74002441 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581676 | AGAGAGTATACTCCC[A/G]GGGCGCCAGCCAGCA | 55666 |
rs74002463 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601548 | AGATGTGAGCCACCA[C/T]GGCTGGCCTCAATTA | 55666 |
rs74369540 | snp | A/G | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587664 | GAAAAAAGAAACAAA[A/G]AAAAAAGTTGTTTTT | 55666 |
rs74372286 | snp | A/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631803 | CTTGTATTTAGCTCA[A/T]TTTTTTTTTCCCCGA | 55666 |
rs74615113 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635926 | AACGAGGGACTGGTT[C/T]TCTGATTTGTCACTG | 55666 |
rs74720380 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558937 | GGCCCCTCCCTGTGC[A/G]CCCCAATTCCAGGTG | 55666 |
rs74787657 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600961 | AACTCCACAGAGAGC[A/G]ATGAGCTCACCAACC | 55666 |
rs74869798 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612267 | GTCAGAATTCTTACA[C/T]GCGTATGAGCCCTGT | 55666 |
rs75045041 | snp | A/C | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623799 | CGAGACTCCGTCTCA[A/C]AAAAAAAAACAAAAC | 55666 |
rs75056808 | snp | A/C | 0.128288 | 0.218372 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599807 | CTGTTCCATGAAACT[A/C]GGAAGAATTGTAGGC | 55666 |
rs75076089 | snp | A/G | 0.0520825 | 0.152737 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567805 | GACTCAGACTGGCCA[A/G]GTGTGGAGGCTAACA | 55666 |
rs75078292 | snp | A/G | 0.26271 | 0.249677 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618466 | CTCCGCCTGGCAGCC[A/G]CCCCGTCCGGGAGGA | 55666 |
rs75156940 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616822 | CAAAGACTCACACAC[A/T]GAAATTATGAGACCG | 55666 |
rs75216764 | snp | C/T | 0.10237 | 0.201756 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631401 | TAACGTGTGTGTGCA[C/T]ATATGCATATTAAAG | 55666 |
rs75267021 | snp | A/C/T | 0.0162709 | 0.0889773 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583009 | GCACTCACAACTGAG[A/C/T]GCCCATGTGCGCCAG | 55666 |
rs75271791 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579738 | GTACATGCCCATGTC[A/C]GTATTTCCCTTACGT | 55666 |
rs75305572 | snp | C/T | 0.127944 | 0.218179 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622026 | TCCTGGCAAGCAACA[C/T]GGTCATGTGTATTCT | 55666 |
rs75340968 | snp | A/C | 0.257516 | 0.253569 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564712 | AGAATCGTTTGAACC[A/C]AGGAGGTGGAGGTTG | 55666 |
rs75373514 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624942 | AGACAGGGCCGTGGG[A/G]AGCCACACAGACGAA | 55666 |
rs75416338 | snp | A/G | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611835 | GTAGCTGGGACTACA[A/G]GCGCCCGCCACCACG | 55666 |
rs75458335 | snp | C/T | 0.155987 | 0.23165 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631033 | CAAAAATTAGCTGGG[C/T]GTGGTGGCGGGCACC | 55666 |
rs75634705 | snp | G/T | 0.0588605 | 0.161139 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600010 | AGAGGAGCCAGCAGG[G/T]GTGCGGCTGGGGTCT | 55666 |
rs75659804 | snp | A/T | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564709 | AGGAGAATCGTTTGA[A/T]CCCAGGAGGTGGAGG | 55666 |
rs75697204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606299 | AACATCCAGAAAGGC[C/T]GGAACGCTCCCTCCT | 55666 |
rs75719313 | snp | A/T | 0.0858192 | 0.188533 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631771 | TTCTTTCTCTCTCAT[A/T]TCCTGCATTACCATC | 55666 |
rs75735577 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589184 | AACTCTTCACCTCTG[A/C]TCAACAGAAAAAACA | 55666 |
rs75753772 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606487 | CAGAGAACTGAGGGC[A/G]CGCACTCCATATCTC | 55666 |
rs75782971 | snp | A/G | 0.000728585 | 0.0190725 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629811 | CACGAATTATCTGTT[A/G]CAAACAAAACATGAT | 55666 |
rs75783018 | snp | A/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609008 | TTCTTTTTTTAATTA[A/T]TTGTTTTTTGTTTGT | 55666 |
rs75859807 | snp | C/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559727 | TTGGGTTGTTTCCAG[C/T]TTTTTTTTTTTTTTT | 55666 |
rs75923948 | snp | A/T | 0.387832 | 0.208572 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595536 | CATATATATATATAT[A/T]TTTTTTTTCTTTTCT | 55666 |
rs75932482 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579663 | GCTGTCCCTGACACA[C/T]GGACCATGCCCCTTC | 55666 |
rs75946256 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574192 | GAATTCATCTTCAAA[C/T]CTAATTAAGCTCTAA | 55666 |
rs75979626 | snp | A/G | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587666 | AAAAAGAAACAAAGA[A/G]AAAAGTTGTTTTTTT | 55666 |
rs75983706 | snp | A/T | 0.0103295 | 0.0711199 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556795 | ACACGTAAAACAGTG[A/T]TATCTTGGAGACAAG | 55666 |
rs76029942 | in-del | -/AAAAAAAG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623478 | TCAAAAAAAAAAAAA[-/AAAAAAAG]CAAAACTCTGTCTCA | 55666 |
rs76147980 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626545 | GGAACGACAGCTTCA[A/G]ATGCTCAACAGGACC | 55666 |
rs76149409 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603226 | ATAAAGGAAAGCAGG[A/G]TAAAAGGAAATGAAT | 55666 |
rs76207987 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599840 | AGAGAGCTAAATTAT[A/C]AACAGGAAATTAAAT | 55666 |
rs76360834 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623850 | TAACACAGAATGGTG[C/T]GACTAAATCATAAAA | 55666 |
rs76397700 | snp | A/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638057 | TGTGACAGTTTTTTT[A/T]AACTATGTTAAATTA | 55666 |
rs76403168 | snp | A/G | 0.149999 | 0.229128 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593652 | CACTACTGTACCCAG[A/G]TATCAGCCTACATGT | 55666 |
rs76407518 | snp | A/G | 0.15698 | 0.23205 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582485 | TAGCTCACTGCAGCC[A/G]TGAACTCCTGGGCTA | 55666 |
rs76413942 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600604 | CGGCTTCTCTCCTTC[C/T]CGGGTTGTGCTGCAC | 55666 |
rs76461600 | snp | G/T | 0.14933 | 0.228835 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615707 | CTTCCCTGCCCAGAG[G/T]GGGCAGCTGAGTCCG | 55666 |
rs76475803 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630508 | CTGATCTCGAGCTCC[A/G]GGGCTCAAGTGATCC | 55666 |
rs76512198 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596800 | GGCCTTCATTGATCA[A/G]GAAGAACTTCTTGAA | 55666 |
rs76591845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573593 | CACTATTGTACTTGA[C/G]TAGTCTTAAAAAATA | 55666 |
rs76616962 | snp | C/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627953 | AAAAAGAAATTTGTA[C/T]TGAATGAAAATATCC | 55666 |
rs76699003 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578364 | TCCCCAACAGGACAC[C/T]TCCACAGTTTCCAAG | 55666 |
rs76703483 | in-del | -/AAAGAACGAAAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576634 | CTTTGTATAAAAGAC[-/AAAGAACGAAAA]CCTGGCGTGTGTTTG | 55666 |
rs76927892 | snp | C/T | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564704 | GAGGCAGGAGAATCG[C/T]TTGAACCCAGGAGGT | 55666 |
rs76941779 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612913 | CACCTCACATGGATG[A/C]GCACACACAACCACC | 55666 |
rs76986510 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583842 | ATGTAAATGTATGTC[C/T]ACATCCATGTGCAAA | 55666 |
rs76995970 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560524 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 55666 |
rs77024233 | snp | A/T | 0.444444 | 0.157135 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602380 | AGAGACCCTCCCTGT[A/T]TAAAAAAAAAAATTA | 55666 |
rs77025041 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600610 | CTCTCCTTCTCGGGT[G/T]GTGCTGCACCTTTTA | 55666 |
rs77082882 | snp | A/T | 0.5 | 0 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561765 | TAATTCTTTTTTTTT[A/T]AATATTGTTTTTTTG | 55666 |
rs77120433 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557534 | CGTGCTGTCCAGCCT[C/T]TGCCCAGTGGTGGGG | 55666 |
rs77143985 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593266 | CTCTTCTGCTTGGAA[A/C]TGGGTGGGGAGCTGC | 55666 |
rs77176320 | snp | C/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595453 | AAAAAACCCGTTTTG[C/T]TTTTTTTTTTTGAGA | 55666 |
rs77340164 | snp | C/G | 0.0919752 | 0.193722 | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81564109 | ACACACACACACACA[C/G]ACACACACAAAGAGC | 55666 |
rs77411083 | snp | C/G | 0.158302 | 0.232576 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632565 | GTTATCCACCCACCT[C/G]GGCCTCCCAAAGTGC | 55666 |
rs77429354 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561570 | AGGCCCTGAAGAGAT[C/T]CAACTTAATAACTGT | 55666 |
rs77438833 | snp | C/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636769 | AAGTCCCCGAGAGGG[C/G]CCCAGCCACTACAGA | 55666 |
rs77452943 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587755 | CTTAATGCAAGCTCC[A/G]CCTCCCAGGTTCACG | 55666 |
rs77499545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590280 | TCCCAGTCTCCACTC[C/T]ATCGAAGCCTCCAGA | 55666 |
rs77528546 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610480 | AGTGCAGTGGTGATC[A/G]TGGCTCCCTGCAGCC | 55666 |
rs77609718 | in-del | -/AGAAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607409 | AAAAAAAAAAAAAAA[-/AGAAA]TCTGTATCTTTAAGG | 55666 |
rs77692287 | snp | C/T | 0.139903 | 0.224452 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635568 | ACAGTCTCATTCTGT[C/T]GCCCAGGGTGGAGTC | 55666 |
rs77711070 | snp | G/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588332 | AGGATTCTAAAAAAG[G/T]TCCCGAAACATCTCC | 55666 |
rs77771502 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605706 | CCAGTGGCGGGACAC[A/G]GGGTTATAGGAGGAT | 55666 |
rs77886370 | snp | C/T | 0.139903 | 0.224452 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590758 | CGTAGTGCACATGGC[C/T]GTCAAACATGCATCA | 55666 |
rs77888432 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569918 | TCCCCAAAGCAGCAC[C/T]GAGTTGAGTTGATGC | 55666 |
rs77917997 | snp | C/T | 0.48 | 0.0979796 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611831 | CTGGAACTGCAGGCG[C/T]CCGCCACCATGCCCG | 55666 |
rs77985450 | snp | G/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571685 | TGGAGACCCAAGCAA[G/T]GGGGGTTCGCTGCCT | 55666 |
rs78020514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574466 | AGGCCTACACACCAT[C/T]TTAAAAGGCAATTAC | 55666 |
rs78128702 | snp | A/G | 0.204496 | 0.245824 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616674 | GGCGGAGCTTGCAGT[A/G]AGCCAAGATGGTGCC | 55666 |
rs78135377 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596049 | AAGGATAAAAAGCTA[A/C]CAAAAAGAGGAACAA | 55666 |
rs78136412 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594365 | ATTAACATAATTAAC[A/G/T]TGTGAAAGATGCCTA | 55666 |
rs78141409 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601052 | CGATGAGTTGTAGCT[G/T]CGACTGGCTCCCATG | 55666 |
rs78164439 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591447 | CTCTGGAGTAAAACA[A/G]AAAAAAAAAAAAAAA | 55666 |
rs78180918 | snp | C/T | 0.48 | 0.0979796 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611821 | AGGCGTCCGCCACCA[C/T]GCCCGGCTAAATTTT | 55666 |
rs78184483 | snp | G/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605840 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 55666 |
rs78185164 | snp | C/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595454 | AAAAACCCGTTTTGC[C/T]TTTTTTTTTTGAGAT | 55666 |
rs78253309 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577215 | CCCTCAGCTCCCCAC[A/G]GCGCTCTGACCCGCC | 55666 |
rs78271869 | snp | G/T | 0 | 0 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562547 | TTTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTCA | 55666 |
rs78291005 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624047 | CCCAGCACTTCGGGA[A/G]GCCAAGGCGGGTGGA | 55666 |
rs78404437 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604357 | ATATCCTTATCCTTA[A/G]TAACATACACTGAAG | 55666 |
rs78476883 | snp | A/G | 0.000165747 | 0.00910197 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622142 | TTCCCCCCATTCCCT[A/G]CTTCCTCCTCAGAGG | 55666 |
rs78496197 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608612 | GTAACTTTCAAAGGC[A/G]TGTGACCCCTTCTCA | 55666 |
rs78500024 | snp | C/T | 0.123798 | 0.215808 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600622 | GGTTGTGCTGCACCT[C/T]TTACCAGGGCTGCAA | 55666 |
rs78524626 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600664 | TGCAGGGCCCAGCTG[A/T]TGTGTGCTGCACAGC | 55666 |
rs78548347 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629488 | CCACCACGCCCAGCC[A/G]TGAAATATTTTTACA | 55666 |
rs78551747 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576999 | TAGCAATTCATCCCA[A/G]GTAATTTAAAGCATG | 55666 |
rs78593750 | snp | G/T | 0.158632 | 0.232706 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636705 | CGGGGAACCGGGGTC[G/T]TAAGTCCCCTGGGGA | 55666 |
rs78608009 | snp | A/G | 0.132751 | 0.2208 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628614 | AAACCTACCTACAAC[A/G]AAGGCTAATGGATGT | 55666 |
rs78832721 | snp | G/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605839 | CTTTTTTTTTTTTTT[G/T]GAGACGGAGTCTCGC | 55666 |
rs78909301 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638234 | TGTACAGGTTACTGA[A/G]GTTTTATTACTACTC | 55666 |
rs78912734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589698 | GAAATCAAGACTGTT[A/C]AACTTTTGAAAAAAA | 55666 |
rs78916319 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581675 | AAGAGAGTATACTCC[C/T]GGGGCGCCAGCCAGC | 55666 |
rs78949153 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637948 | AAAAAAAAAAAAAAA[-/AAA]AGACGTCACTTCACA | 55666 |
rs78983222 | snp | C/G | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636422 | GGTGGGGAGGGAGCT[C/G]TGTAACGTCCCCGTC | 55666 |
rs79020017 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577174 | GGCTCCTTGAAGGAA[C/T]GCTGTTCCCTTGCTG | 55666 |
rs79059060 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597922 | ACATGGTGAAATCCC[A/G]TCTCTACTAAAAATA | 55666 |
rs79100643 | snp | C/T | 0.206029 | 0.246103 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623516 | AAAAAATAAAAAACC[C/T]GGCCGGGCGCGGTGG | 55666 |
rs79214902 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602156 | TCAGTGGCATACACC[A/G]ATAGTCCCAGCTACT | 55666 |
rs79218805 | snp | A/C | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598094 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 55666 |
rs79283578 | snp | A/G | 0.107694 | 0.205546 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575303 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 55666 |
rs79356272 | snp | A/C | 0.155987 | 0.23165 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635186 | CACCACTAAAAATAA[A/C]AAAGACATCAGCCAT | 55666 |
rs79411706 | snp | A/C | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619880 | TGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAGGT | 55666 |
rs79414920 | snp | A/C | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598095 | GCAAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAA | 55666 |
rs79428460 | snp | A/G | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589867 | AAAAAAAAAAAAAAA[A/G]ATTGTTAAACATTGT | 55666 |
rs79439699 | snp | C/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574287 | AAATGCCCCTCTCTC[C/T]TTTTTGTGTCATGCT | 55666 |
rs79440371 | snp | C/T | 0.257454 | 0.249889 | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81564181 | GGGTGATGTGATCAA[C/T]CATACCCCAACCTCA | 55666 |
rs79459378 | snp | C/T | 0.149999 | 0.229128 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584520 | GCACTTGCTTTACAA[C/T]TAAAAGCAAGACAAA | 55666 |
rs79502364 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620516 | AAATAAATAAATAAA[A/T]AAATGCAAACCGGTG | 55666 |
rs79530192 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625478 | GGTAAAGAAACAAAT[C/G]ATAAAAGAACAATCA | 55666 |
rs79761164 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603750 | TTCATTTTATTTTTC[C/T]ATTGGATTTCAAGTG | 55666 |
rs79781703 | snp | A/G | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574084 | AGGAGGCAAAAATCA[A/G]ATCCAGTCAAACTAA | 55666 |
rs79788351 | snp | A/C | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623797 | AGCGAGACTCCGTCT[A/C]AAAAAAAAAAACAAA | 55666 |
rs79807898 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635973 | GGAGGAGTGTGTGAC[A/T]ATTTTTTTTTTTTTT | 55666 |
rs79931779 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582980 | AGGCCTCCTCCCTGC[A/G]GCGCCGCCCCTGCGC | 55666 |
rs79973778 | snp | A/T | 0.10237 | 0.201756 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580011 | AAGCCTCCTCTCCTG[A/T]CTCACCAGGGAGCTC | 55666 |
rs79975064 | in-del | -/CCC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631466 | TTTTTTTTTTTCCCC[-/CCC]CACGGCAAGCCTAAA | 55666 |
rs79995833 | snp | A/T | 0.5 | 0 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561767 | ATTCTTTTTTTTTTA[A/T]TATTGTTTTTTTGTA | 55666 |
rs80106978 | snp | C/T | 0.102014 | 0.201495 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619301 | AGAATGGCATGAACC[C/T]GGGAGGTGGAGCTTG | 55666 |
rs80156290 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585053 | CGTGCGCCTGTAGTC[C/G]TGGCTACTCGGGAGG | 55666 |
rs80158493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559570 | GCACTCCCACCACAG[A/G]CACACTTTGAAGTGC | 55666 |
rs80174869 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559826 | CAACCTCCACCTCCC[A/G]GGTTCAAGCGGTTTT | 55666 |
rs80220350 | snp | G/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559728 | TGGGTTGTTTCCAGC[G/T]TTTTTTTTTTTTTTT | 55666 |
rs111229703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597046 | TGAACCCGGGAGGCA[C/T]TGCTAGCGGTGAGCA | 55666 |
rs111254647 | snp | C/G | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569216 | AATTAACGACTCCTA[C/G]CAATTCTGAGAATGT | 55666 |
rs111255097 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565027 | TCAGGACCTGGTGAC[C/T]GAGGGTCCGGAAGAC | 55666 |
rs111441266 | in-del | -/TT | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595454 | AAAAACCCGTTTTGC[-/TT]TTTTTTTTTTTGAGA | 55666 |
rs111442033 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582392 | GCATCTAGCGGTGTT[C/G]TGTGTGTGTATGTAT | 55666 |
rs111454246 | snp | A/G | 0.216649 | 0.247765 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627166 | GAGGCCGAGGCAGGC[A/G]GATCATGAGGTCAGG | 55666 |
rs111457296 | snp | A/G | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603013 | CACACACACACACAC[A/G]CATATAAAAGTCAGA | 55666 |
rs111485493 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557685 | GAGAGCAGACAGCCC[A/G]CGGTGGGCAAGCTGG | 55666 |
rs111493103 | snp | A/C/G | 0.5 | 0 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565426 | ATCCAGGGCACCACC[A/C/G]GCAGTGGGGAGCTGT | 55666 |
rs111494113 | snp | C/T | 0.45889 | 0.13735 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611629 | TGCTGGGATTACAGG[C/T]GTGAGCAACTGCGCC | 55666 |
rs111539205 | snp | C/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624801 | CCGCCACACGCGAGC[C/T]GGGAGAAAAGGCCAC | 55666 |
rs111581626 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592848 | AATTGGCCGGGTGTG[C/T]TGGCATGCGCCTGTA | 55666 |
rs111582165 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611642 | GGTGTGAGCAACTGC[A/G]CCTGGCCAAGTCCAT | 55666 |
rs111647845 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595537 | ATATATATATATATT[A/T]TTTTTTTCTTTTCTT | 55666 |
rs111652008 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570943 | TTCCTTTATAAAAGA[A/G]GAGGAAAGAAGTGGG | 55666 |
rs111664870 | snp | A/G | 0.168785 | 0.236441 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618967 | AATGGATTAAGGGCG[A/G]TGCAAGATGTGCTTT | 55666 |
rs111675062 | in-del | -/A | 0.215144 | 0.247558 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563169 | AACCTACGCTTCCTG[-/A]GGTCAAGTGATTCTC | 55666 |
rs111675438 | in-del | -/AC | 0.278399 | 0.248382 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605815 | TAGGGCAAAAAACAA[-/AC]ACATTTTCTTTTTTT | 55666 |
rs111795626 | snp | C/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579919 | ATTCTCCTCTGTGAG[C/T]TCACTCTCGGCAGCC | 55666 |
rs111802010 | in-del | -/C | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624787 | AGCGGTGGGTAAGCC[-/C]GCCACACGCGAGCTG | 55666 |
rs111812808 | snp | A/G | 0.494315 | 0.0530107 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618808 | TCGGATGGTTGCTGT[A/G]TCTGTGTAGAAGGAA | 55666 |
rs111818424 | snp | C/T | 0.123452 | 0.215605 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581789 | AAGGACTGGAGGCTG[C/T]GTGATCTCTGTGGCA | 55666 |
rs111878172 | snp | A/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602706 | AACTCCGTCTCAAAA[A/T]TAAAAAAAAAAAAAA | 55666 |
rs111971600 | snp | G/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635028 | GAGACCTCATCTCTA[G/T]AAAAAAATGTTTTTA | 55666 |
rs111993243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563545 | ACTGCACTCCAGCCT[A/G]GGCAACAGAGTGAAA | 55666 |
rs112005655 | snp | C/G | 0 | 0 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560908 | TTCAGCCACACTGAT[C/G]AATGTGTAACGGCTT | 55666 |
rs112015086 | snp | C/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631463 | TTTTTTTTTTTTTTT[C/T]CCCCACGGCAAGCCT | 55666 |
rs112029003 | snp | A/C | 0.127944 | 0.218179 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597074 | GCAGAGATTGCGCCA[A/C]TGCACTCCAGCCTGG | 55666 |
rs112068034 | in-del | -/A | 0 | 0 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562957 | AAAAAAGGAGGGGGG[-/A]AAAAAAAAAAGGTCA | 55666 |
rs112109180 | snp | A/C/T | 0.0229266 | 0.104809 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575056 | CACCAGGATCTGAGC[A/C/T]GCCACAGGATAACTC | 55666 |
rs112118980 | snp | C/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622619 | ACAGTGGCATGATCT[C/T]GGCATACTGCAACCT | 55666 |
rs112144740 | snp | A/G | 0.369142 | 0.219784 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618745 | CATGATGACAATGGC[A/G]GTTTTGTGGAATAGA | 55666 |
rs112149849 | snp | A/G/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557408 | TGATGTGAATGCCGG[A/G/T]ACTTCAGAGTAAGGG | 55666 |
rs112160687 | in-del | -/CCC | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631462 | TTTTTTTTTTTTTTT[-/CCC]CCCCCACGGCAAGCC | 55666 |
rs112259517 | snp | A/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567223 | TGAAAAAATTAATCT[A/T]TCAACAAGCTTCTTG | 55666 |
rs112271845 | snp | A/G | 0.24932 | 0.249999 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575295 | TTTAGTAGAGACGGG[A/G]TTTCACCGTGTTAGC | 55666 |
rs112292147 | snp | A/G | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560298 | GACACCTGCCGTTCC[A/G]GCTACTCAGGAGGCT | 55666 |
rs112330164 | in-del | -/A | 0.334412 | 0.235318 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602708 | CTCCGTCTCAAAATT[-/A]AAAAAAAAAAAAAAA | 55666 |
rs112364254 | snp | A/G | 0.269538 | 0.249235 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611261 | GGAGGCAAAGGTTGC[A/G]ATGAGCTGAGATTGT | 55666 |
rs112367240 | snp | A/G | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582955 | CCCAAGGAGCCTCCC[A/G]GCCAGGGCCAGGCCT | 55666 |
rs112417725 | snp | A/G | 0.486266 | 0.0817214 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611193 | GACGTGGTGGCAAGC[A/G]CCTGTAATGCCAGGA | 55666 |
rs112461634 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588209 | TGAAATGAACAGAGT[A/G]TCAGTAAACTGCGGG | 55666 |
rs112556803 | snp | C/T | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581862 | CAGGAAAGAGCATCC[C/T]GAAAGCAGAGGCGCA | 55666 |
rs112572666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616959 | GGCAGGCACCAAAGT[C/T]AGTGGCTCTTCCCAA | 55666 |
rs112612275 | snp | A/C | 0.363568 | 0.222716 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585578 | GAGGCAGGAGAATCG[A/C]AGAACTCAGGTGGCA | 55666 |
rs112629728 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557130 | CTGGATTATGGTGCT[A/G]GTAGCATGAGAGGGT | 55666 |
rs112640115 | in-del | -/A | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590672 | TTATAGTTTTGGATG[-/A]AAAAAAAACCCTCAA | 55666 |
rs112716983 | snp | C/T | 0.0261704 | 0.111357 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604725 | GTCCACATGCCTGTA[C/T]TTCTGTAGAGTTAAC | 55666 |
rs112840005 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561701 | ATCCTCCCATTTCAG[C/T]CTCCCCAGAAGCTGG | 55666 |
rs112851577 | snp | C/G | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586100 | GACCAGCCTGCCCAA[C/G]GGGGTAGGAGGGAGG | 55666 |
rs112883845 | snp | C/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633348 | GAATGTTCCTTCAAA[C/T]GATGACTCTGGAACA | 55666 |
rs112936165 | snp | C/G | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570561 | GAACCAAAGTCCACA[C/G]AGCCCATCCCAGATG | 55666 |
rs112947854 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605068 | GATCAAGACCATCCT[A/G]ACCAACATGATGAAA | 55666 |
rs112984754 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588703 | CAATGGTCGGATTTG[A/G]TGTTACTGATCTCAA | 55666 |
rs113002720 | snp | C/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617805 | CTGCGATTGCAGGCG[C/T]GCGCCGCCACGCCTG | 55666 |
rs113010177 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585669 | CCATTTCTGGGGGGG[C/G]GGGGAAAGAAAGAAA | 55666 |
rs113036580 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610813 | AAAAATTAGCCGGGC[A/G]CGGTGGCGGGCGCCT | 55666 |
rs113059955 | snp | A/G | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585675 | CTGGGGGGGGGGGGA[A/G]AGAAAGAAATCAGAG | 55666 |
rs113116451 | in-del | -/A | 0.333491 | 0.235646 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563393 | CCCTATCTCTTAAAG[-/A]AAAAAAAAAAAACAC | 55666 |
rs113150170 | snp | A/G | 0.214239 | 0.247429 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617690 | TCCGTCTCTTTCCAC[A/G]GTCTCCCTCTCATGC | 55666 |
rs113192992 | snp | A/C | 0.5 | 0 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560701 | AACAAACAAACAAAC[A/C]ACAACAACAAAAAAC | 55666 |
rs113230225 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595952 | GTTTTATGCTGTTAA[A/G]TTGTTCAGAATTTTT | 55666 |
rs113273770 | snp | A/G | 0.114387 | 0.210022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597038 | GAATGGCGTGAACCC[A/G]GGAGGCATTGCTAGC | 55666 |
rs113318717 | snp | A/G | 0.00524458 | 0.050939 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559353 | ATGGCTGCAGTGGCC[A/G]TGTGTGTGGAGCCCC | 55666 |
rs113337188 | snp | A/C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628461 | GAGGTTGCAGTGAGC[A/C/T]GAGATCATGCCACTG | 55666 |
rs113393346 | snp | C/T | 0.237882 | 0.249706 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577463 | TCAACGCCCTCTTCT[C/T]TTCTCCCTCTGAACC | 55666 |
rs113443569 | snp | A/G | 0.149665 | 0.228982 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632200 | AATCTGGTCTTAAAC[A/G]CCTACCTCAGGTGAT | 55666 |
rs113450373 | in-del | -/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595535 | ACATATATATATATA[-/T]TTTTTTTTTCTTTTC | 55666 |
rs113474032 | snp | C/T | 0.178144 | 0.239451 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603016 | ACACACACACACACA[C/T]ATAAAAGTCAGACAT | 55666 |
rs113482962 | in-del | -/TCTT | 0.5 | 0 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567216 | AGGTGAAAAAATTAA[-/TCTT]TCTATCAACAAGCTT | 55666 |
rs113488612 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636315 | ATCAACATCATTTAC[A/G]ACATTCCTTTTAAAG | 55666 |
rs113493245 | snp | A/C | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576116 | GAGGAGACACAGATA[A/C]CTTGTTTTACAATGA | 55666 |
rs113528673 | snp | C/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598658 | GCAGTGCCTGTGTGC[C/T]GTGTGATCCTTAGGC | 55666 |
rs113538157 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626260 | GGCGGAGGTTGCAGT[C/G]AGCCAAGATCGCGCC | 55666 |
rs113538317 | snp | C/T | 0.148996 | 0.228688 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577513 | TCCGGGTTAGCTCAA[C/T]GCACTCTTCTCTTCT | 55666 |
rs113574144 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578604 | GGGAAGGGGAAGCAA[C/G]GCACCTTCTTCACAA | 55666 |
rs113610620 | snp | A/G | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585674 | TCTGGGGGGGGGGGG[A/G]AAGAAAGAAATCAGA | 55666 |
rs113611088 | snp | A/G | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575084 | CTCAGAAAAAACAAA[A/G]CTTTCAGACACTCGG | 55666 |
rs113626478 | snp | A/G | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571664 | ACTGCTTGATGCTCC[A/G]GTGACTGGAGACCCA | 55666 |
rs113723749 | snp | C/T | 0.150333 | 0.229274 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562296 | ATAATCCCAGCACTT[C/T]GGGAAGCCGAGGTGG | 55666 |
rs113739992 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571830 | AAAACTGTGAGCATT[G/T]CAGCAACACCGCATG | 55666 |
rs113795259 | snp | C/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632609 | GTGCACCACCACACC[C/T]GGCCTCCCTTATTTC | 55666 |
rs113884796 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577500 | TGGCTCATCTACTTC[C/T]GGGTTAGCTCAACGC | 55666 |
rs113915083 | snp | C/G | 0.360842 | 0.224085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585670 | CATTTCTGGGGGGGG[C/G]GGGAAAGAAAGAAAT | 55666 |
rs113948975 | snp | A/G | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630413 | TGACCTCAGCCTCCC[A/G]AGAGCTGGAACCACA | 55666 |
rs113953791 | in-del | -/G | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589714 | ACTTTTGAAAAAAAG[-/G]AAAAGAAAAGGCTCA | 55666 |
rs113961852 | snp | A/G | 0.5 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610811 | CAAAAAATTAGCCGG[A/G]CGCGGTGGCGGGCGC | 55666 |
rs113964075 | snp | C/T | 0.158302 | 0.232576 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633106 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 55666 |
rs114130927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565354 | GCCTGGCAGGGAGGC[C/T]GAGTCTCTACTCGTT | 55666 |
rs114184180 | snp | A/G | 0.030665 | 0.119967 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571523 | AGGTGTGTCCCCTGG[A/G]GACCACCCTGGACGG | 55666 |
rs114240800 | snp | A/G | 0.0134861 | 0.0810011 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556492 | AGTGTGTCACCCCCA[A/G]GCCTCACTCCTTGCT | 55666 |
rs114373438 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612647 | TGCAGAGACAACCTT[C/T]GCTCAGACAATTTCA | 55666 |
rs114427627 | snp | A/G | 0.0182019 | 0.0936463 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556571 | TGACCACATGTACCT[A/G]TCCACAAAGCAGTGA | 55666 |
rs114477265 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568547 | ATGCAGGCGTGACAG[C/G]AAATCGGACCTGGCC | 55666 |
rs114522147 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583566 | GAGGCTGGCTGGCCC[C/T]AGTCCCTCGGGAAGC | 55666 |
rs114553523 | snp | A/G | 0.105214 | 0.203807 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579125 | CACGCCTGTAGTTCT[A/G]GCACTTTGGGAGGCA | 55666 |
rs114553858 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633760 | CCAGAGTGGGAGTGC[A/G]ATGGCGCGACCTCGG | 55666 |
rs114604810 | snp | C/G | 0.0178098 | 0.0926698 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558965 | GTGCCACGTAGAGGC[C/G]AGAGGTCTTTCCAAC | 55666 |
rs114698572 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574624 | GGTTGTGGCCCCAAC[A/G]CCTCGCCACCCGCCA | 55666 |
rs114809458 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633205 | ATTCTAGATTCAATA[A/C]CCCAGAAAAACGTTT | 55666 |
rs114821053 | snp | C/T | 0.00835141 | 0.0640778 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559023 | GGCGTGAGGAGCCGC[C/T]CTGCGTTTCCAGTCT | 55666 |
rs114825682 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573819 | CACGTATTGCTCCCC[A/G]CCCCATCAAAGGCTA | 55666 |
rs114862195 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598723 | CGTCACGAGGCCACA[A/G]GAGCAGCAGTTGAGT | 55666 |
rs114945751 | snp | C/T | 0.0614824 | 0.164198 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635218 | CGTGTTGGCGAGCAC[C/T]TGCAACCCCAGCTAC | 55666 |
rs115037544 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592223 | GGAGGGATGTGGGAC[A/G]GGAATGCAACAAGTA | 55666 |
rs115073211 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583138 | AGAGATGTTAGTGTG[A/G]CTTTTCAGTGAGCGA | 55666 |
rs115103633 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603398 | GCCAGTAGTTCAAGA[C/T]CAACCTGGGCAATAT | 55666 |
rs115104756 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580666 | GACCCACCAGGGCAC[C/T]CCAAGCTTCTCTACC | 55666 |
rs115108946 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559658 | TGCTGGTTCCTTTTT[A/G]TTGCAGAGGGTGCTT | 55666 |
rs115241527 | snp | C/G | 0.030665 | 0.119967 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624557 | GAGATGAGATCACGC[C/G]ATTACACTCTAGCCT | 55666 |
rs115289931 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626397 | AAATTTAATGAAAAA[C/T]ATCAAATAGCAACTC | 55666 |
rs115352395 | snp | C/T | 0.0314385 | 0.121371 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578233 | CAGCTAGACTGGCCC[C/T]GCCGGGTGCATGCTG | 55666 |
rs115386702 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603959 | CCCAAAAACCAGAAA[C/T]ACAATGTGTAACTAG | 55666 |
rs115468915 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574563 | GGCAGCCGTCAAAGT[A/G]TCAGCAGCTTTATCT | 55666 |
rs115485207 | snp | A/G | 0.0139358 | 0.0823026 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568975 | ACTAGATAACAATCA[A/G]CAGTTACCTTAAATT | 55666 |
rs115775110 | snp | A/C/G | 0.0103333 | 0.0711729 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558967 | GCCACGTAGAGGCGA[A/C/G]AGGTCTTTCCAACAC | 55666 |
rs115939762 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587974 | GCCGCCGCGCCCGGC[C/T]GAAAAAAGTTAATAT | 55666 |
rs115999932 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629284 | TGTAAACTCTGCCTT[C/T]TGAGTCAAGCAATTC | 55666 |
rs116085601 | snp | A/G | 6.72427e-05 | 0.005798 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606652 | AATATCCGTTTCTCA[A/G]CCATGAAAACAAATC | 55666 |
rs116088184 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563491 | AGGAGGATCGCTTGA[A/G]CTCAGGAATTGAAGG | 55666 |
rs116104407 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607066 | CTTTCCTACCAAACT[G/T]TGGTGTTTTTTACCA | 55666 |
rs116108513 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81564126 | CACACACAAAGAGCA[A/G]GGCGGGCTGAAAAAC | 55666 |
rs116111249 | snp | C/T | 0.0360663 | 0.129354 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558729 | CCTGCAGAGGGGAGC[C/T]GTGTCCAGGGCCACT | 55666 |
rs116152183 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576112 | ACATGAGGAGACACA[C/G]ATACCTTGTTTTACA | 55666 |
rs116221179 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625587 | AGCAGAAGAGTCAAC[C/T]TAAACATAGGTGAAT | 55666 |
rs116221520 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588795 | AATATCCAGCCCCAG[A/G]AACGTGACAGAAGCC | 55666 |
rs116224704 | snp | C/G/T | 0.0444908 | 0.142359 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636505 | GAGAGCAGGAGGAGA[C/G/T]AATCAGAGGGAGATT | 55666 |
rs116294739 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601054 | ATGAGTTGTAGCTTC[A/G]ACTGGCTCCCATGCA | 55666 |
rs116341617 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622587 | AGACAGTCTCGTTCT[A/G]TAGCCCAAGCTGGAG | 55666 |
rs116466395 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572896 | AAGGCATGCACAAAT[A/G]AGCGCACACACAAAT | 55666 |
rs116467777 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567170 | AACCGTACTTCCTCA[A/C]AGAGGTGCAGACACT | 55666 |
rs116538116 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588266 | GTAACTGGAGCCCCC[A/G]AAGGAGCGGGAAACA | 55666 |
rs116567357 | snp | C/T | 0.021333 | 0.101051 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556570 | TTGACCACATGTACC[C/T]GTCCACAAAGCAGTG | 55666 |
rs116585775 | snp | G/T | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566815 | GAAGAAAAAGCCAAA[G/T]TCGGACCCCTACACA | 55666 |
rs116655809 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620753 | GGGACAAGCGTGGTC[A/G]TGAGCTGAGAGTTCC | 55666 |
rs116762489 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626603 | CAGCATCCAGGAGAC[A/G]GAGTGGGGAGGATCA | 55666 |
rs116909274 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568283 | CAGGGCAGCCGTGAT[A/G]CAGCACGGACATCTT | 55666 |
rs116940465 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572488 | GAGCCACCGCGTCCG[G/T]CCTTCACTTTTTAAA | 55666 |
rs117067321 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603716 | CTATGCACTATCTGT[C/G]CCTCTAGTCACCCAT | 55666 |
rs117085892 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575983 | TTGCGTGCTGCTGGG[A/T]CTTGTGCCAGCAAAT | 55666 |
rs117233315 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565913 | CCTGGAGGCTGGGAT[A/G]GAGGGCGGAAGTCTT | 55666 |
rs117408790 | snp | C/T | 0.10237 | 0.201756 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585661 | GGAAGACTCCATTTC[C/T]GGGGGGGGGGGGAAA | 55666 |
rs117449251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625719 | CTGAGCGACAGAGTG[A/T]GAATCCAACCAACTC | 55666 |
rs117526336 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631671 | GCTCCAACCATCCGC[A/G]GGACGGGAAGGAAGG | 55666 |
rs117537007 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598237 | TCAAGTAAGATGCCA[A/G]GCCACACCCAGGGAT | 55666 |
rs117550005 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593811 | TGCCCAGTGCCCACT[A/G]CCTGATGCCCCAGCT | 55666 |
rs117665608 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577346 | CACCTCTCCCAGACC[C/T]TTCTCCTTGACCTCT | 55666 |
rs117824378 | snp | A/T | 0.338296 | 0.233889 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572187 | TTTAATTAATTTATT[A/T]ATTTATTTATTTATT | 55666 |
rs117875090 | snp | G/T | 0.00755907 | 0.0610114 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556513 | ACTCCTTGCTGCACC[G/T]GTGCAGTCTGGCCTT | 55666 |
rs117902872 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570221 | GGGCCGCGGTGCCAC[A/G]TGTCGGCTACATGGC | 55666 |
rs117928966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580687 | CTTCTCTACCCGTTC[C/T]GCTGGGGTGGCCCAC | 55666 |
rs118063254 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577104 | AGTAAGCAATGCCTG[A/G]CCACAGCAAGGGGCA | 55666 |
rs118070844 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568262 | GCAGCAAGAGGGAGG[A/T]ATGTGCAGGGCAGCC | 55666 |
rs118110072 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625742 | ACCAACTCTAAAAAG[A/G]AAAACATAAATGAAT | 55666 |
rs118122839 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557422 | GAACTTCAGAGTAAG[A/G]GAAATGCTGGTGGAG | 55666 |
rs137946753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607988 | TTCTGGTAGGGTGTA[C/T]AGAGAGCCAACAGGA | 55666 |
rs137975292 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572191 | ATTAATTAATTTATT[A/T]ATTTATTTATTTTTT | 55666 |
rs137978577 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636001 | TTTTTGAGACGCAGT[A/C]TCGCTCTATAGCCCA | 55666 |
rs137996095 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633986 | TTTCTGCCTCAGCCT[A/C]CTGAGTGGCTGGGAC | 55666 |
rs138010515 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592943 | AGCCAAGATTGTGCC[A/C]TGGCACTCCAGCCTG | 55666 |
rs138045712 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631461 | TTTTTTTTTTTTTTT[C/T]TCCCCCACGGCAAGC | 55666 |
rs138128205 | in-del | -/A | -0.970074 | 1.38783 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633333 | GAAGGGGAACATGTG[-/A]AATGTTCCTTCAAAC | 55666 |
rs138184353 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566289 | GTAAGCCAAGATTGC[A/G]CCAATGCACTCCGGT | 55666 |
rs138188650 | in-del | -/AA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610669 | AAAATGACACAAACC[-/AA]AGGCCGGGCGCGGTG | 55666 |
rs138214950 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603074 | CTTGGGAGGCTGAGG[C/T]AGGAGGATTGCTTGA | 55666 |
rs138298541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563973 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGGAG | 55666 |
rs138332158 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557763 | TCCTGACCCTCCACA[A/G]TAGCTCTGCCGTGAC | 55666 |
rs138337750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560961 | CCTGATGACTAATGA[C/T]AGTGACTGTTCCTGC | 55666 |
rs138343184 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625137 | ACCAGGCCCAGCTGA[C/G/T]GAGCAGGACCAGGGG | 55666 |
rs138354082 | in-del | -/CTTGTCTCTGAAGCTACTGAC/GTTTCTGCTTGTCTCTGAAGCTACTGAC | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614568 | GAGTCAGACTTAAGG[lengthTooLong]GTACTGCTTTCCAAA | 55666 |
rs138475619 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608650 | TTCTCTCATTCACAC[A/G]TTCACTGGCTATAAG | 55666 |
rs138564347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579138 | CTAGCACTTTGGGAG[G/T]CAAGGCAGGTGGATT | 55666 |
rs138572440 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577542 | CTCCCTCTGAACCAC[A/G]GCTTGGCTCATCTAC | 55666 |
rs138602634 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566723 | TCTCCTTCAGGGAAA[A/G]GTTCTGAGTCAGTGG | 55666 |
rs138614878 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564299 | ATAAAAAGCAACAAC[A/G]AAGCCCCAAGAATTA | 55666 |
rs138631972 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586336 | TAATCCCAGCACTTT[C/G]GGTGGCCTCACGCCT | 55666 |
rs138633239 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628882 | CATATCTACAATTCA[C/T]ACTTTTTTTTTTTTT | 55666 |
rs138675493 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624897 | CCAATAAACAATAAG[A/G]AAGATGGAAAGAGAT | 55666 |
rs138814632 | in-del | -/ATTAA | 0.441705 | 0.160466 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638082 | AAATTACATTAATTG[-/ATTAA]ATTATGTTAGTAATT | 55666 |
rs138858708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592159 | GTGCTGTCGGCAGGG[A/G]CGCCCCGCACCCTAT | 55666 |
rs138878497 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589650 | TTGGCTCCACAAACA[A/G]GTGCCACTAAGGACA | 55666 |
rs138924194 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604316 | CACTGGATCAATAGT[A/G]GCAAATGTACCGGTT | 55666 |
rs138935101 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575640 | GCTGTGTAGAGACTG[C/G]GCCCCCCACACTACG | 55666 |
rs138955126 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634982 | GTAGGAGGATCCCTC[A/G]AGCTCAGAGACCAGC | 55666 |
rs138956659 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614353 | TCATAAAATCCTCCA[A/C]ATATAAGGAGTCCAC | 55666 |
rs138988560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583519 | AAGAGAAAAGCCCCA[C/T]GTCCTGCCACCTGGC | 55666 |
rs139000013 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626114 | AGATTGCGCCACTGC[A/G]CTCCAGCCCAAGCGA | 55666 |
rs139050589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584905 | AGCACGGTGGCTCAC[A/G]CCTATAATCCTAGCA | 55666 |
rs139217282 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616486 | CTGTAATCCCAGCAC[A/G]TTGGGAGGCCGAGGC | 55666 |
rs139254460 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637389 | GAAACAGCATTCCAA[A/T]CTTCTCTCCATGCAC | 55666 |
rs139316335 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583940 | TTAATTTTGCTTTCT[A/G]AGTTTTACCCCTTAT | 55666 |
rs139337381 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594919 | TGTGCTCCAGCCTGG[C/G]TGACAGAGCAAGAAC | 55666 |
rs139363089 | snp | A/G | 0.10237 | 0.201756 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585119 | AGGTTGCAGTGATCT[A/G]AGATCGCACCACTAC | 55666 |
rs139402492 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556478 | GCAGGAACACAGGCA[A/G]TGTGTCACCCCCAGG | 55666 |
rs139403266 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562159 | ATCACTTGAACCCAG[A/G]ACGTGGAGGTTGCAG | 55666 |
rs139409281 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633238 | ACAATATATAGCATT[A/C]GGTAAATACTTCCAC | 55666 |
rs139480702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599859 | AGGAAATTAAATGAT[A/G]ATTGATGACGGAGCA | 55666 |
rs139547041 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594334 | TCACTTGTAAAATAG[C/T]TAACATGTATTAATT | 55666 |
rs139547131 | snp | A/G | 0.00223751 | 0.0333729 | synonymous-codon, nc-transcript-variant, missense | NPLOC4 | GRCh38.p7 | 17:81559379 | GCCCCCGACGGCGCC[A/G]TACTCATGGAGACCT | 55666 |
rs139585886 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590832 | GAGATAGAGCTGGCC[A/G]CCATGAAGCTCTCAA | 55666 |
rs139614040 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581340 | GGCAACACAGCCAGA[C/T]TCCAACGCAAAAAAA | 55666 |
rs139652049 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572862 | TCCAGAAACCGAGTA[C/T]TTGGACATTAATAAA | 55666 |
rs139754645 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567949 | CCAGGCTTGGTGGCG[C/T]GCACCTATAATCCCA | 55666 |
rs139776026 | snp | A/G | 0.000899361 | 0.0211866 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81565557 | CTTCCATGTCTGGGC[A/G]AGCTCCTCATTTCTG | 55666 |
rs139795994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620740 | GGGCAAGAGCAGCGG[A/G]ACAAGCGTGGTCGTG | 55666 |
rs139804465 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619375 | CAGTGAGACTCCGTC[G/T]CAAAAAACAAAAACA | 55666 |
rs139840280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565056 | ACACGCAATGCCTGC[A/G]GTCCGTTCCGTAGTG | 55666 |
rs139847729 | snp | A/G | 4.975e-05 | 0.00498724 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629684 | CAGTAAGAGTAGAGG[A/G]TGAAAAATATCCTGA | 55666 |
rs139966500 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584413 | AGAAACTTACAATAA[C/T]GCATGGAAATAAAAA | 55666 |
rs139974685 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615903 | GCCATGCATCTGGAG[C/G]AGAACCAGGGATGAT | 55666 |
rs139985147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582293 | CTGCACGTCACATCC[A/G]TACCAGGAGGTTTTC | 55666 |
rs140009289 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633860 | ATAGGCGCCCGCCAC[C/T]GCGCCCAGCTAATTT | 55666 |
rs140100887 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606967 | CTAAGGATGATTCTA[A/T]TGGAAGCTCTACCTA | 55666 |
rs140113956 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605820 | GGCAAAAAACAAACA[C/T]TTTCTTTTTTTTTTT | 55666 |
rs140180260 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599118 | ACATGGTGAAACATC[A/G]TCTCTATTAAAAATA | 55666 |
rs140198548 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637116 | CTCGCTCAATACGCT[A/C/T]CCCTCGGGCGCGAGG | 55666 |
rs140230927 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621103 | CCTTCAAGAAAGAAA[C/G]AAAAGGAAAGAAGGA | 55666 |
rs140287472 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582745 | CAGAAGACAGTCAAG[C/T]GCCTCCTGGCTGTAC | 55666 |
rs140290190 | in-del | -/AC | 0.256619 | 0.249912 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576001 | GTGCCAGCAAATACA[-/AC]AGTGGGTTACAGGGC | 55666 |
rs140306891 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577861 | GTCCCCAAGGCCACA[A/G]GGAACTGACATGTGG | 55666 |
rs140393264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577190 | GCTGTTCCCTTGCTG[C/T]TCCTATGTCCCCTCA | 55666 |
rs140394336 | in-del | -/T | 0.0611083 | 0.163768 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630069 | AATTCCTAATCACTA[-/T]TTTATAGAGTATATG | 55666 |
rs140396056 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629463 | GAAGTGCTGGGATTA[C/T]AGGTGTGAGCCACCA | 55666 |
rs140424500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562472 | TGAACCCGGGAGGTG[A/G]AGGCTGCAGTGAGCT | 55666 |
rs140432578 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627815 | GTGGTGCACACCTGT[A/G]ATCCCAGCTACTTGG | 55666 |
rs140477288 | snp | G/T | 0.000385579 | 0.0138795 | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563873 | CAGCAAACCAAATAC[G/T]ACATGTTTTCATTTA | 55666 |
rs140514271 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560671 | GAGGTTGCAGTAAGC[C/T]GAGATCTCAAAACAA | 55666 |
rs140532350 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585148 | ACACTCCAGCCTGGG[C/G]GACAGAACGAGACTC | 55666 |
rs140585878 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573931 | TGTGTCCTCCTTCCA[C/T]GTGACGAGTGGCTGC | 55666 |
rs140635034 | snp | A/G | 1.65839e-05 | 0.00287953 | synonymous-codon, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81589016 | CTCCGGGGCGTCCTT[A/G]CATGGCAGCAAACAC | 55666 |
rs140800811 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575272 | GCCCGGCTAATTTTT[G/T]TCTATTTTTTAGTAG | 55666 |
rs140806674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616892 | ATGGAAGAAGAGGGT[A/G]AGTGACAGAGGCTAT | 55666 |
rs140847055 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576947 | ACACACAGACCCTTC[C/G]AGTACATAGTAAGCT | 55666 |
rs140917194 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592073 | ATACCTGAGTACAAC[C/G]AAAGGGGAAAGGGGA | 55666 |
rs140922502 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627660 | AGAATTGCTTGAACC[C/T]GGGAGGCTGAGGCAG | 55666 |
rs141049031 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631462 | TTTTTTTTTTTTTTT[C/T]CCCCCACGGCAAGCC | 55666 |
rs141056040 | in-del | -/CTAT | 0.0158469 | 0.0875917 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556398 | GTGACTGCCAGGCTC[-/CTAT]CTGAGGCTCAGAGAG | 55666 |
rs141104570 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635591 | GTGGAGTCCAGTGAC[A/G]CCACCTAGGCTCACT | 55666 |
rs141112414 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560435 | AACAACAGGCCGGGC[A/G]CGGTGGCTCATGCCT | 55666 |
rs141136290 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571774 | AACCCCTAGGTTGAC[A/G]TCAAGGAAATAAAAA | 55666 |
rs141152097 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625811 | TTGGGGAAAAAAAAA[-/A]CAGCCTTAGGAACCC | 55666 |
rs141222513 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630501 | TCCCAGGCTGATCTC[C/G]AGCTCCGGGGCTCAA | 55666 |
rs141242637 | in-del | -/T | 0.171057 | 0.237209 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563353 | CTGGGATTACAGGTG[-/T]TGAGCCAGCCACCGG | 55666 |
rs141299644 | snp | A/G | 0.10237 | 0.201756 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605853 | TTGAGACGGAGTCTC[A/G]CTCTGTCACCCAGGC | 55666 |
rs141335897 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602487 | AGGCGGGTGGATCAC[C/G]AGGTCAGGAGTTTGA | 55666 |
rs141382368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561890 | GCTATGAGACATCAT[A/G]CCCAGCCTGCTTCAT | 55666 |
rs141386799 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625915 | ACACTTTGGGAGGCC[A/G]AGTTGGGCAGATCAC | 55666 |
rs141421364 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583867 | TGCAAATGCCTATAC[A/G]TGTCTTCAAGAAAAT | 55666 |
rs141485617 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638741 | GTGGGGGCCACAAGA[C/T]ATGAGCCAGTTTATC | 55666 |
rs141491584 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622653 | CATCCCAGGTTCCAG[A/T]GATTCTCCTGCCTCA | 55666 |
rs141523076 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578333 | CACTGTGAATGGCCA[C/T]CTCGGCGCACCCTGC | 55666 |
rs141620602 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629378 | TGTATTTTTAGTAGA[C/T]GGGGTTTCACCATCT | 55666 |
rs141720288 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624266 | TCTACTAAAATACAA[A/C]AATTAGCTAGGCGTG | 55666 |
rs141757046 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586615 | ACTGTCTCAAAAAAA[A/G]AAAAAAAAGATGCTT | 55666 |
rs141813295 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590093 | AGTCATGGTATTGTA[C/T]ACACAGCAGCCTCTG | 55666 |
rs141851329 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557477 | GTGGATAAGGACGAG[C/T]GAGTGGGAGAGGAAC | 55666 |
rs141852957 | in-del | -/AC/TA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602923 | ATATATGTATATATA[-/AC/TA]CACACACACATATAT | 55666 |
rs141912560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585867 | GGTAGTGTGCGCCTA[C/T]AGTCCCAGCTACGCG | 55666 |
rs141935448 | in-del | -/C | 0.149665 | 0.228982 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637623 | GCCAAAATGGTGAAA[-/C]CCCCGTCTCTACTCA | 55666 |
rs141937518 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599003 | CTTAGAAACTCATAT[C/T]TTAGGCCAGGCACGG | 55666 |
rs141951243 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613950 | ACATACACACGTAAG[C/T]ACAGACACGCATAGG | 55666 |
rs141999520 | in-del | -/T/TT | 0.499937 | 0.0055907 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629192 | CTCTTATGAAATACT[-/T/TT]TTTTTTTTTTTTTTT | 55666 |
rs142071257 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557134 | ATTATGGTGCTGGTA[C/G]CATGAGAGGGTGTGT | 55666 |
rs142082182 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558361 | GCAGGGCAGCCTCAG[A/G]GCAGGCGCCACCACT | 55666 |
rs142090895 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588568 | GCCCAGGCTGGTCTT[G/T]AAGTTCTGGACTCAA | 55666 |
rs142118087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608178 | GAAAACCAAGCTGAC[C/T]CAGAGGCCAGGCTCT | 55666 |
rs142133512 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574625 | GTTGTGGCCCCAACA[C/T]CTCGCCACCCGCCAG | 55666 |
rs142138894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564942 | GGCACTCGGGCTGCA[C/T]GAGGCACCACGGTGC | 55666 |
rs142156975 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604430 | GTTGTGCACGTGCAC[C/T]GGTGTGTGACAAAGG | 55666 |
rs142172065 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570424 | CTGGCCTGCTCAGGC[A/G]CGTCCCTTGGGAAGG | 55666 |
rs142260670 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573724 | ACTTGCCTCTACCCT[C/T]CCAGAGAAAAATGGT | 55666 |
rs142281414 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609447 | GAGTAGCTGGGACTA[C/T]AGGCGTGAACCACCA | 55666 |
rs142330001 | snp | C/T | 6.62877e-05 | 0.00575669 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622144 | CCCCCCATTCCCTGC[C/T]TCCTCCTCAGAGGAC | 55666 |
rs142437269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627683 | TGAGGCAGGAGAATT[A/G]CTTGAACACAGGAGG | 55666 |
rs142504917 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588826 | TTTAGTGACAAGCAG[C/G]GTTCAACCACAGCTG | 55666 |
rs142533863 | snp | C/T | 0.029116 | 0.117091 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561026 | GCAATGGCGCAATCT[C/T]GGCTCGCTGCAACCT | 55666 |
rs142537228 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605821 | GCAAAAAACAAACAT[A/G/T]TTCTTTTTTTTTTTT | 55666 |
rs142539876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625138 | CCAGGCCCAGCTGAC[A/G]AGCAGGACCAGGGGC | 55666 |
rs142541666 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623753 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 55666 |
rs142574213 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558939 | CCCCTCCCTGTGCGC[C/T]CCAATTCCAGGTGCC | 55666 |
rs142579867 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623228 | TGTAATCTCAGCACT[A/G]TGGGAGGCCAAAGCA | 55666 |
rs142613855 | snp | A/T | 0.0379877 | 0.132479 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634458 | GTGGGAAAAAAAAAA[A/T]GGCCTTGTCTGAAAC | 55666 |
rs142623583 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581981 | GCTGACAGCAGAGAC[A/T]TGCTTCCATGGTGGA | 55666 |
rs142664023 | snp | A/C | 0.029116 | 0.117091 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624341 | GAGAATTGCTTGAAA[A/C]CAGAAGGCAGAGGTT | 55666 |
rs142684222 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593521 | CAGAATTCTGTGTGT[C/T]GGCAGCCTACATTAA | 55666 |
rs142776720 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605069 | ATCAAGACCATCCTG[A/G]CCAACATGATGAAAT | 55666 |
rs142821788 | in-del | -/GCT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613125 | GGAAACTGATAAAAA[-/GCT]AAAAAAAAAAAAAAA | 55666 |
rs142926109 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575395 | CGTGAGCCACAGCGC[C/T]CAGCTGACACTTGGT | 55666 |
rs142950434 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591161 | TGGACTGGGCTTGGC[A/G]CAGTGGTTCACGCCT | 55666 |
rs142963921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573120 | ACCAAAGCTTTTCAT[G/T]AAAGATTCTGCAAGA | 55666 |
rs142977650 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636482 | ACAAGGCACTTGCTG[A/G]GAAGCGGGAGAGCAG | 55666 |
rs142983146 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626146 | AGAGTGAGACTTCAT[C/T]TCAAAAAAAAAAAAA | 55666 |
rs143025803 | snp | C/T | 0.00290271 | 0.0379859 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606843 | AAGCAACTTAAACAT[C/T]ACATTGGTGAAAAGT | 55666 |
rs143125202 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601190 | ATGCAGAAACCCCAG[C/T]CATAAGAATAGGAAA | 55666 |
rs143146254 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582297 | ACGTCACATCCGTAC[C/G]AGGAGGTTTTCAGCT | 55666 |
rs143159951 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581612 | GGCCACCTCTCCTCA[C/G]TCCCCCACAACGATT | 55666 |
rs143191209 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620860 | ACTTTTTTTTAAAAA[A/T]TTACCAGCTAGATTT | 55666 |
rs143248597 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558186 | TCTCCCTCTATTGGT[A/G]CACTATCAATTGTGC | 55666 |
rs143254712 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622459 | TCACAAAGGTGTCAA[C/T]TAAAATGAATAAAGT | 55666 |
rs143264220 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565777 | CTTACATCTATAAAC[A/G]CAAGTGCTAAATTGA | 55666 |
rs143330142 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603737 | AGTCACCCATCAATT[C/T]ATTTTATTTTTCTAT | 55666 |
rs143335833 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578040 | TGGATTTCAGCCCCA[C/G]TCACTCCTCTAAACT | 55666 |
rs143357495 | snp | A/C | 0.0513262 | 0.151752 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617880 | TGGCCGGGCTGGTCT[A/C]CAGCTCCTAACCAAG | 55666 |
rs143358054 | snp | C/G | 0.45866 | 0.137698 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618493 | AGGAAGGTGGGGGGT[C/G]AGCGACCCCGCCCGG | 55666 |
rs143442100 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574857 | CGTCTCTACAAGACT[A/G]TCTCCAAACAAACAA | 55666 |
rs143444181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81639051 | GAAGTTATTTCAGCC[C/T]ACACCCAGGAATGAA | 55666 |
rs143462216 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625877 | TGAGGGTTGGGCGCG[-/G]GAGGTTCAAGCCTGT | 55666 |
rs143530846 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584472 | TAAAAATAATCCTAC[A/G]GCAAACTCACAGTTA | 55666 |
rs143566157 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587675 | AAAGAAAAAAGTTGT[-/T]TTTTTTTTTTTTTTT | 55666 |
rs143572748 | in-del | -/C | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561951 | CATCCTGAGCTGATC[-/C]TTTGTGTCTTGTGTA | 55666 |
rs143573743 | snp | A/G | 0.149999 | 0.229128 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594515 | GGCGCAGTGGCTCAC[A/G]CCTGTCATCCCAGCA | 55666 |
rs143588599 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629000 | TCTCCTGCCTCAGCC[G/T]CACCAGCAGCTGGGA | 55666 |
rs143692984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625106 | GGCAAGAGCACACTT[G/T]CCAGCAGTGGTCATC | 55666 |
rs143765393 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566352 | AAAATAATTCATATA[C/T]GAGAAACGGATAAAG | 55666 |
rs143779780 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582918 | CACAGCCAGCCTCCC[A/G]ATTCGAAGAAACACA | 55666 |
rs143813960 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579547 | CCTGTGGCTTCCTGT[A/G]AGCAAGCTGATCCCC | 55666 |
rs143855383 | snp | A/C/G | 0.0287397 | 0.11645 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599150 | AAAAATTAACTGGGC[A/C/G]TTGTGGCGGGTGCCT | 55666 |
rs143888606 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616166 | TGCTAAAAATAAAAA[A/T]AAAAATTAGCCGGGG | 55666 |
rs143925907 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598153 | GCTTCTGCCCAGAGA[C/G]CTTAAAAAGAATGTT | 55666 |
rs144069153 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561027 | CAATGGCGCAATCTC[A/G]GCTCGCTGCAACCTC | 55666 |
rs144076880 | in-del | -/TA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603018 | CACACACACACATAT[-/TA]AAAAGTCAGACATGG | 55666 |
rs144126681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620314 | CAGCTTGGCCAACTT[A/G]GTGAAACCCCACCTC | 55666 |
rs144174509 | snp | A/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556710 | ACTTTAAGAAACTTA[A/T]CGAGGAGCCAAGGTT | 55666 |
rs144195177 | snp | A/G | 0.00143205 | 0.0267203 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565639 | GGAAGGTTCCTCTTC[A/G]CTGTGCCTAAGGTGA | 55666 |
rs144198198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630431 | AGCTGGAACCACAGG[C/T]TTGCACCACCACACC | 55666 |
rs144220765 | snp | C/G/T | 0.008755 | 0.065668 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590211 | CCGTGGGCAGACCTG[C/G/T]GAGCCCAGCTCCTCC | 55666 |
rs144394284 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609036 | TGTTTGTTTTGAGAC[A/G]GAGTCTCACTCTGTC | 55666 |
rs144395763 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576972 | TAAGCTTCGGCAACA[C/T]AATCCTAGTTCTAGC | 55666 |
rs144437181 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574682 | AAGGTCTTGACACCA[A/G]GAGAAATCCAGGGAT | 55666 |
rs144456941 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633351 | TGTTCCTTCAAACGA[C/T]GACTCTGGAACAAGA | 55666 |
rs144478241 | snp | C/T | 0.000914495 | 0.0213638 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567402 | CTCAAGTGGACACCA[C/T]ACTTGGACACGCACC | 55666 |
rs144509347 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576409 | GGGCTAGGAAACTCA[-/T]GTATACGGAGGTCTA | 55666 |
rs144555451 | snp | A/T | 0.0252325 | 0.109451 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568049 | GCACCACTGCACTCC[A/T]GCCTGGGTGATAGAG | 55666 |
rs144568368 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619863 | CAGCCTGGGCAACAG[A/G]TTGAGACTCCGTCTC | 55666 |
rs144637953 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616939 | GGATTCTAGGACATG[G/T]AAGTGGCAGGCACCA | 55666 |
rs144676952 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575876 | AGAATCTCTTCTGTC[A/G]ATGGCAGTTTCTTGA | 55666 |
rs144736151 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581813 | TGTGGCAGAAGGGTC[A/G]TAGCCTGCCACATCC | 55666 |
rs144773729 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628607 | GACCAACAAACCTAC[A/C]TACAACAAAGGCTAA | 55666 |
rs144806057 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590940 | GGATTTTCTCCCTGC[C/T]CCAAACTCAAATGCT | 55666 |
rs144842117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588844 | TCAACCACAGCTGAC[A/G]AACGGCTGCTATAGG | 55666 |
rs144955635 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582773 | TACAACAGTCTACGA[C/G]TGTGAGTCTTGTCCC | 55666 |
rs145016595 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592128 | GCGAGGCCTCCGCAT[A/C]CCAGCCAGGACCTGA | 55666 |
rs145032979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589641 | CGCACACACTTGGCT[C/T]CACAAACAGGTGCCA | 55666 |
rs145036177 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630560 | GGTGTGAGCCACAAC[A/G]CCAGCTATTACTTAC | 55666 |
rs145098300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81577378 | TAGAGCAGCCATCCT[C/T]GGAGTTGCTCAACGC | 55666 |
rs145219362 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610453 | AGGCTCTCACTCTAT[A/C]GCCCAGGCTGGAGTG | 55666 |
rs145237530 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600727 | GCAAGGTCTACACAC[A/C/T]CTGCCTGTTTTAAAA | 55666 |
rs145254831 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637818 | GGGCACCTGTAATCC[C/G]AGCTACTCGGGAGTC | 55666 |
rs145272431 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612108 | TAACAACAATGAAAA[A/C]ACCTTGTCCCACGGC | 55666 |
rs145362067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576254 | AAATCCTAAAAGCAC[A/G]GAAAGAGTATGTAGG | 55666 |
rs145370803 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562718 | CTGAGGCGGGAGGAT[C/T]GCTTGGGCCCAAGAG | 55666 |
rs145392377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595020 | AGTGCAAAAACTTCG[C/T]AGTCAGCTTGAACAC | 55666 |
rs145477352 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559240 | TGGGCCCGGTCCTAG[C/T]CAGCAGAGGGCAGGC | 55666 |
rs145521762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617272 | AAAAAATCAGATTAC[A/G]TATTTATTTATATAC | 55666 |