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 |