SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs145571822 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559984 | AGGTGATCCACCCAC[C/G]TTGGCCTCCCAAAGT | 55666 |
rs145606780 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574695 | CAAGAGAAATCCAGG[G/T]ATCGATGTCTTTGTT | 55666 |
rs145640115 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611733 | TGGGAGGCCGAGGCG[G/T]GTGGATCACAAGTCA | 55666 |
rs145670674 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560882 | ACTTGACATTGTCGC[G/T]TTTTTTTCATTTCAG | 55666 |
rs145670940 | snp | C/G | 0.00641199 | 0.0562573 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597332 | CTTAAAAAAAGGAAA[C/G]TAGCTTTTAAACATC | 55666 |
rs145746415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568747 | CTGCTGGCAGAAGAC[A/C]CAAAGCAACACATTT | 55666 |
rs145752697 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634020 | AGGTGCACGCCACCA[C/T]GCCCGGTTAATTTTT | 55666 |
rs145788685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621586 | TCCGTAAAGGACCAG[C/T]CAATACTTTCAGCTT | 55666 |
rs145795281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613204 | TAGTAAAACTTAAGA[C/T]TTAACATTTCTTCAT | 55666 |
rs145834081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591042 | GTGCTTGGTGGCATA[A/G]ATGACACTGAAAGAA | 55666 |
rs145855428 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630235 | TATACAAACATTAGA[C/T]AGTCTTCAAGAGTCC | 55666 |
rs145877428 | in-del | -/AA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623465 | CAAGACTTTGTTTCA[-/AA]AAAAAAAAAAAAAAA | 55666 |
rs145897722 | in-del | -/TCTT | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567220 | GGTGAAAAAATTAAT[-/TCTT]CTATCAACAAGCTTC | 55666 |
rs145999146 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586031 | GTCTCATGCATGTAA[C/T]CCCAGCACTCTGTGA | 55666 |
rs146009747 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584300 | TTTCTAGCCTATTCT[C/T]GCTAACAGAGGGCAA | 55666 |
rs146010503 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625372 | CAGGTGGGCGCATCT[G/T]TGTCTGAGCCCAGGC | 55666 |
rs146022607 | snp | C/T | 0.102014 | 0.201495 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623287 | CCAGCCTGGTCAACA[C/T]AGTGAAACCGTCTCT | 55666 |
rs146076835 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634940 | GGTAGCTCAGGACTG[C/T]AATCCTAGCAATTTT | 55666 |
rs146131421 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575522 | GCACAGAGCCACTTC[A/G]TCCTCACAAACACAC | 55666 |
rs146142268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573288 | GAAATGATTGCCAAG[C/T]AAATCTCCCTGAGGT | 55666 |
rs146146597 | snp | A/G | 0.149665 | 0.228982 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637078 | CGCCCGCCCGGCTCC[A/G]CCAGCCGCCGACGTC | 55666 |
rs146156256 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633855 | GGATTATAGGCGCCC[A/G]CCACCGCGCCCAGCT | 55666 |
rs146242422 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558872 | ATGGGGGCAGGGAGG[C/T]CAAACAAAAAGCACT | 55666 |
rs146253575 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589768 | TCTGAGAGGGCAGGG[C/T]GGGAGGACTGCTTGA | 55666 |
rs146357057 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583391 | TGTTTTGAAGTTAAA[A/C]GAATAGAAAAGGAAA | 55666 |
rs146364607 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572519 | TTACTTCAAATCTTA[C/T]TGAAGTGTATGGATA | 55666 |
rs146374036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608371 | ACTGCACTGTGGCCA[C/T]GCAGCCAGGCGCCTG | 55666 |
rs146375552 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567905 | ACATGGCGAAACCCC[A/G]TCTCTACTAAAAATA | 55666 |
rs146384897 | snp | A/C/G | 0.000856376 | 0.0206769 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604537 | AGGAACTTGAATCCC[A/C/G]TCATGTTTACCTGAG | 55666 |
rs146426825 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618603 | GTCAGCCCCCCGCCC[A/G]GCCAGCCGCCCGTCT | 55666 |
rs146448567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612209 | TTACGAGGGCGCCGG[C/T]GGCCGTCCCTCCGGG | 55666 |
rs146518378 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556858 | GACAACAGTTGAGTG[C/T]GCAGGAAGGACACAC | 55666 |
rs146520567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620528 | AAAAAAATGCAAACC[A/G]GTGATTACTGTTAGG | 55666 |
rs146559859 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565700 | CCCCAACATCAAGAC[A/G]TATTTCTGAGGACAT | 55666 |
rs146573045 | snp | A/T | 0.178144 | 0.239451 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628361 | CTACTAAAAATACAA[A/T]AAATTAGTCAGGTAT | 55666 |
rs146635630 | snp | A/G | 0.0414363 | 0.137845 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568162 | GTCCCCCGGTGGAGA[A/G]TGGGCTGCGGGAGGG | 55666 |
rs146728912 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557473 | CGTGGTGGATAAGGA[C/T]GAGCGAGTGGGAGAG | 55666 |
rs146757075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584652 | ACGTGTAGGAAATGC[A/G]AAAGACTAAACTTAT | 55666 |
rs146800021 | in-del | -/CA | | | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81564095 | TCAAAACACACACAC[-/CA]ACACACACACACACA | 55666 |
rs146801649 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596793 | GAGATCCGGCCTTCA[C/T]TGATCAAGAAGAACT | 55666 |
rs146870379 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565261 | TCTGATGTACAGGTT[C/T]ATAAAATTTACAGGG | 55666 |
rs146881365 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563521 | GCTGTAGTGAGCTAT[C/G]ATCACTCCACTGCAC | 55666 |
rs146893806 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585102 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGATC | 55666 |
rs146940523 | snp | A/G | 0.0170251 | 0.090679 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635702 | GTGAGTCACCGCGCC[A/G]GGCCTGGAGACCTAT | 55666 |
rs146979498 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569331 | AAACTACACCATATC[C/T]GGGCAGCCTCCGGCC | 55666 |
rs146999057 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602587 | GGCACCTGTAATCCC[A/C]GCTATTCAGGAGGCT | 55666 |
rs147105056 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622050 | GTATTCTGGTCAGTT[C/G]ATAAGACCATAATGA | 55666 |
rs147114956 | snp | A/G | 0.489893 | 0.0703642 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618585 | TCCGGGAGGGAGGTG[A/G]GGGGTCAGCCCCCGC | 55666 |
rs147150257 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629438 | CGTGATCCACCCGCC[C/T]TGGTCTCCCGAAGTG | 55666 |
rs147254884 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580118 | ATTCCCCCAAGGTGG[A/G]GTTCTCCTCAGCCAT | 55666 |
rs147264880 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576755 | GTGCACACAGAGGCT[A/G]CTCACAAAGAAAACA | 55666 |
rs147335686 | snp | C/T | 0.00347594 | 0.0415438 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597368 | AAGATAGACGATGAA[C/T]GGCTGGGCGCAGTGA | 55666 |
rs147371911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632667 | CTGTGAGGTTACCAC[A/G]AGTGTTACATTAAAC | 55666 |
rs147371951 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590713 | CAGTTTCTTTGACAA[A/C]AAGAATCACTTATGA | 55666 |
rs147466321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615822 | ATCCCATCTGCCTCT[A/G]TCCAGTACACAGCAA | 55666 |
rs147473845 | in-del | -/GTGCCCA | 0.0283406 | 0.115616 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593794 | CTGCTCCCCTCCTGG[-/GTGCCCA]GTGCCCAGTGCCCAC | 55666 |
rs147476303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609882 | GCAAAGTAAATCAAC[A/C]ATGATAAGCACGGAG | 55666 |
rs147625599 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570162 | GCATCTCTGGCCTGA[C/G]CTGGCCCTTCATGGG | 55666 |
rs147635681 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606254 | GAGGAAGGCGAGGCA[A/G]GCTACTCAGAGGCGG | 55666 |
rs147696150 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573997 | GGCTGTGATGGGGGC[A/G]CTAAAGACACAGGGC | 55666 |
rs147730846 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627349 | GTGAGCCGAGATCGC[A/G]CCACTGCATTCCAGC | 55666 |
rs147732003 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585063 | TAGTCCTGGCTACTC[A/G]GGAGGCTGAGGCAGA | 55666 |
rs147740737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624331 | GCTGCGGCAAGAGAA[C/T]TGCTTGAAACCAGAA | 55666 |
rs147764681 | in-del | -/TG | 0.00795532 | 0.062565 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607666 | GCCCCCACTAGAGAC[-/TG]TGTTCCTTGACCTAG | 55666 |
rs147830211 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605824 | AAAAACAAACATTTT[C/T]TTTTTTTTTTTTTTT | 55666 |
rs147835803 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602085 | GTGCATGCATGCGTG[C/T]GTGTATGTGCTTACA | 55666 |
rs147846660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638704 | AGTCAAAACTGTCCT[C/T]TTGTGCTGAGTCGGT | 55666 |
rs147940505 | snp | A/G | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557474 | GTGGTGGATAAGGAC[A/G]AGCGAGTGGGAGAGG | 55666 |
rs147950307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588848 | CCACAGCTGACAAAC[A/G]GCTGCTATAGGCAGA | 55666 |
rs147994280 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574982 | CCTGCTTTAGAAAAG[A/G]TAAATGAAATCCTGA | 55666 |
rs148015555 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632702 | TCTTCAACCATTATG[A/C]AGATGAAAACTGTCA | 55666 |
rs148058164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590021 | TCATCTGGAGGCAGA[A/G]AGATGGGGAAGCGGG | 55666 |
rs148073718 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605826 | AAACAAACATTTTCT[C/T]TTTTTTTTTTTTTGA | 55666 |
rs148108994 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585625 | GAGATCAGGCCACTG[C/T]ACTCCAGCCTGGGAG | 55666 |
rs148128404 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613900 | CAACACTGCATGTGC[C/T]GGTTGCATGTATCTC | 55666 |
rs148129514 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636321 | ATCATTTACAACATT[C/T]CTTTTAAAGAGGAAT | 55666 |
rs148181044 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606899 | CTAAGTATCTTATAC[C/T]TCCTGAACAGTGTCT | 55666 |
rs148269428 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561592 | AATAACTGTTTTACA[G/T]TTTTTATTTTTTTAA | 55666 |
rs148279390 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593297 | TGAGCCTCTCAGGAA[C/G]CCATGTTGCTGACGG | 55666 |
rs148319019 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558332 | GGTGACCCAGCTCTC[C/T]CACCCAGGCCATCGC | 55666 |
rs148321826 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622530 | AAAACATTTAAGACT[C/T]TGAAGCAAACAAGAG | 55666 |
rs148362945 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578295 | CACTCCGCGTGGCTT[C/G]CTCTCACACACTCTA | 55666 |
rs148428547 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623752 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 55666 |
rs148435199 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567803 | CTGACTCAGACTGGC[A/C]AGGTGTGGAGGCTAA | 55666 |
rs148444072 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581924 | TAGCCTCGCTATGCC[C/G]TGGATGGAGTCCCAG | 55666 |
rs148480266 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620204 | AGACACTCAAGTAAC[A/G]AAAGAATAAAGAGCC | 55666 |
rs148497542 | snp | C/T | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575881 | CTCTTCTGTCGATGG[C/T]AGTTTCTTGATTAAT | 55666 |
rs148595272 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630291 | TTTTCTAATTGTTAC[A/T]TTTTTTTTGCTTTTT | 55666 |
rs148601777 | snp | C/T | 0.00953873 | 0.0683987 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556860 | CAACAGTTGAGTGCG[C/T]AGGAAGGACACACCA | 55666 |
rs148643690 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598909 | AACCCAAGGTGGTGG[C/T]AACAGAGAAAATGAA | 55666 |
rs148654943 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616177 | AAAAAAAAAATTAGC[C/T]GGGGGTGGTGGCGGG | 55666 |
rs148706946 | snp | A/G | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609327 | CTGGCCAATTTAACT[A/G]TTTTAGAGATGGGGT | 55666 |
rs148815976 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611937 | TGCACTCCAGCCTGG[A/G]TGACAGAGCGAGAGT | 55666 |
rs148932048 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625095 | GTGGGGATGAAGGCA[A/C]GAGCACACTTTCCAG | 55666 |
rs148965469 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634085 | CCGTGTTGCCCAGGC[A/T]GGTCTCAAACTCCTG | 55666 |
rs148973859 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582852 | GCTGGGCTCTGGGGC[G/T]GCACATAAAGCTCCA | 55666 |
rs149005915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591119 | GGAGCCACGGTGCAG[A/G]CATCTGGTTAGGACA | 55666 |
rs149065774 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626318 | GAGACTCCATCTCAA[A/G]AAAAAAAAAAAAGAA | 55666 |
rs149217864 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562916 | GCACTTCAGCCTGGG[A/T]GACAGAGTGAGAACC | 55666 |
rs149283524 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604209 | GACAGTGACTGCTGC[A/G]TGGTGGAAGAGACAC | 55666 |
rs149293034 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619713 | GTGAAACCCTGTCTC[C/T]ACTAAAAATACAAAA | 55666 |
rs149301596 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628967 | CACTGCAAGCTCCGC[C/T]TCCTGGGTTCACATC | 55666 |
rs149342427 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585284 | CTGGAGATGACCGAC[A/G]ACAGAGAAGCATCAA | 55666 |
rs149344870 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615706 | GCTTCCCTGCCCAGA[A/G]GGGGCAGCTGAGTCC | 55666 |
rs149441782 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575850 | TGGGAATATGCTATA[A/G]TAAGTGATTCAGAAT | 55666 |
rs149495344 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572481 | CAGGCGTGAGCCACC[A/G]CGTCCGGCCTTCACT | 55666 |
rs149496536 | snp | C/T | 0.00993419 | 0.0697739 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636104 | CAGCCTCCCAAGTAT[C/T]TGGGATTACAGTGCG | 55666 |
rs149503965 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584132 | AGGTTTTGTTTACAA[A/G]GCATGTCACCTCCAA | 55666 |
rs149513129 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593097 | AAGACTCTGAATGCC[C/T]GCTACACACTTGTGT | 55666 |
rs149553541 | snp | G/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558056 | CATTAAGGCAAAGAA[G/T]CATCGAGATGCCCAC | 55666 |
rs149653370 | snp | C/T | 0.0033574 | 0.0408341 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608680 | GCAACAACTGCCAGC[C/T]ACACAAAAAGGAATT | 55666 |
rs149661416 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559011 | TCAACAGGATTAGGC[A/C/G]TGAGGAGCCGCTCTG | 55666 |
rs149775522 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568381 | CCAAGTCCCCTGGGC[A/G]GATGGGCACTGAGGG | 55666 |
rs149822142 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619203 | AAGAATGATCAATTA[-/A]AAAAAAAAAAAAAAA | 55666 |
rs149822567 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621572 | GCCAGCACCCGTGTT[C/G]CGTAAAGGACCAGTC | 55666 |
rs149829417 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565066 | CCTGCGGTCCGTTCC[A/G]TAGTGTCCACCAGCA | 55666 |
rs149831680 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630037 | CTCAACTCTTAGTTT[A/C]ACTCAGAAAACAACT | 55666 |
rs149883823 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626422 | CAACTCCAGGAAGTT[C/G]AGCAAACTCTCTCAA | 55666 |
rs149945859 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577227 | CACGGCGCTCTGACC[C/T]GCCCCACCCCATCAC | 55666 |
rs149989796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600247 | GAGAGAGCCAGTACC[C/T]GACACAGCCCGGCCA | 55666 |
rs149998212 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637795 | AAAAATTAACTGGGC[A/G]TGGTGGCGGGCACCT | 55666 |
rs150029755 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562686 | GGACATGGTGGCTTA[C/T]CACTGCAATCTCAGC | 55666 |
rs150039814 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595018 | AAAGTGCAAAAACTT[C/T]GCAGTCAGCTTGAAC | 55666 |
rs150095363 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603511 | TGAGGCAGGAGGATC[A/G]CTTGAGCCCAGGAGG | 55666 |
rs150137512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81564204 | CAACCTCAGCATCAG[A/G]CAATATACCCAGGTG | 55666 |
rs150169696 | in-del | -/AT | 0.291843 | 0.246473 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602932 | TATATACACACACAC[-/AT]ATATATATATACACA | 55666 |
rs150191556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624375 | GTGAGCCAAGATGGC[A/G]CCATTGCACTCCAGC | 55666 |
rs150262497 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614077 | GTCAAAAGATCAAGA[C/T]CATCCTGGCCAACAG | 55666 |
rs150310952 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582759 | GCGCCTCCTGGCTGT[A/G]CAACAGTCTACGAGT | 55666 |
rs150375413 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614886 | ACTGCTGCCAACAAG[-/AC]ACACACACAGGGGAC | 55666 |
rs150410776 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627907 | CGCCACCACATTCCA[A/G]CCTGGGCGACAGAAA | 55666 |
rs150451380 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585161 | GGCGACAGAACGAGA[C/T]TCTGTCGCCAAAAAA | 55666 |
rs150536652 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594653 | GCTGGCAGGCTCCTA[C/T]AGTCCCAGCTACTCG | 55666 |
rs150590272 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590131 | GAAACCTACACGGCC[A/G]CCACACAGAGTTAAT | 55666 |
rs150613321 | in-del | -/ACACAC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602981 | TATATATACACAAAT[-/ACACAC]ACACACACACACACA | 55666 |
rs150717699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562045 | TCCAGACCAGCCTGA[C/T]CAACATGGTGAAACC | 55666 |
rs150746336 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565055 | GACACGCAATGCCTG[C/T]GGTCCGTTCCGTAGT | 55666 |
rs150750598 | in-del | -/AAG | 0.245631 | 0.249962 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570939 | TAACTTCCTTTATAA[-/AAG]AAGAGGAAAGAAGTG | 55666 |
rs150833404 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573807 | CTATTTCCATTTCAC[A/G]TATTGCTCCCCGCCC | 55666 |
rs150836502 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637343 | ACCCAAAAATAACTA[A/C]TGCTGCGTATTATAG | 55666 |
rs150841455 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583894 | AAATAACAAAAAAAA[C/T]TGGTATTATACTCTA | 55666 |
rs150895705 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578844 | AGGGTGCTAGGGGGC[A/G]TCCATTTTCTTCTTA | 55666 |
rs150951926 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584953 | GGGCAGATTGCCTGC[A/T]GAGCTCAGGAGTTCA | 55666 |
rs150961650 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624158 | AGGTGTGGTGACTCA[C/T]GCCTGTAATCCCAGC | 55666 |
rs150971168 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634573 | TATTTCTAGGCAAAG[A/T]CACCAATGATTAACA | 55666 |
rs151002180 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582260 | ATGACGGGCATGAAA[A/G]GGCAAAGCTGAAGAT | 55666 |
rs151118923 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592072 | AATACCTGAGTACAA[C/T]GAAAGGGGAAAGGGG | 55666 |
rs151162510 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557405 | GAATGATGTGAATGC[C/T]GGAACTTCAGAGTAA | 55666 |
rs151163905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621072 | AAGGAAGGAAGGAAG[G/T]ATCAAGATGCAAAAC | 55666 |
rs151206776 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576990 | TCCTAGTTCTAGCAA[G/T]TCATCCCAAGTAATT | 55666 |
rs151215693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616375 | TGGATCCTTCAGGAT[G/T]CCTCAAGACCAAGTT | 55666 |
rs151276020 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566201 | GACAGGCGTGGTTGC[A/G]GGCACCTGTAATCCC | 55666 |
rs151339538 | in-del | -/AT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603015 | ACACACACACACACA[-/AT]TATAAAAGTCAGACA | 55666 |
rs151339902 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612736 | ATCTAAAATAAACAA[-/A]TGTACATATGCATAA | 55666 |
rs180671233 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557327 | TGAACAAAGAGTAAC[G/T]CAAAACCAGAATCAG | 55666 |
rs180682329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575769 | CGGACCCCAACAGCC[A/G]TCTCACACTGAGTAA | 55666 |
rs180688312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607154 | ACCTGTGCCACTGAG[C/T]GGGCATGAGGCTCCT | 55666 |
rs180689820 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585062 | GTAGTCCTGGCTACT[A/C/T]GGGAGGCTGAGGCAG | 55666 |
rs180700203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624913 | AAGATGGAAAGAGAT[A/G]AGGCTGGCGAGGCAG | 55666 |
rs180720869 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616586 | ATAGAAAAAATTAGC[C/T]GGGCATGGTGGCAGG | 55666 |
rs180724193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598930 | AGAAAATGAAACTTA[A/G]AGGGTTAATTATGCA | 55666 |
rs180759612 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564291 | ACAAACAAATAAAAA[A/G]CAACAACAAAGCCCC | 55666 |
rs181034424 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638000 | TGGATACCAGGAAAC[C/T]GGAAGACTAAATGTA | 55666 |
rs181123640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631857 | CAGGCTGGAGTACAA[C/T]GGCGCAATCTTGGCT | 55666 |
rs181217938 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559156 | CCCTTGTTCCTCCAG[A/G]GCTGCCCACTATGGG | 55666 |
rs181252902 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637563 | CAGCATTTTGGGAAG[A/C]CAAGGTGGACGGATC | 55666 |
rs181271055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580958 | GAGAGACATGGCATG[A/G]AAGTACAAAATCCCC | 55666 |
rs181271558 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620854 | ATTTAAACTTTTTTT[A/T]AAAAAATTACCAGCT | 55666 |
rs181315459 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602475 | TTTGTGAGGCTGAGG[C/T]GGGTGGATCACGAGG | 55666 |
rs181362627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563487 | ATGCAGGAGGATCGC[C/T]TGAGCTCAGGAATTG | 55666 |
rs181370011 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592454 | TGATTCACACAGACA[C/T]AAAGGGGCTGTCACT | 55666 |
rs181381251 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570682 | CACAAAGAAACCCCA[A/G]TAACACTGGCTGGTG | 55666 |
rs181392628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612581 | TCCCAATACCGCAAA[A/G]TCAGCACCCCGTCAC | 55666 |
rs181404341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631342 | TTTAGCCTAGGAATT[C/T]GAGATCAGCCTGGCC | 55666 |
rs181413163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575521 | TGCACAGAGCCACTT[C/T]GTCCTCACAAACACA | 55666 |
rs181453184 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598808 | CAGCACTACCTGACA[A/C]ACAACTCTTCCCATC | 55666 |
rs181473794 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602324 | GGCCAAGGCAGTAGG[A/C]TCACTTGAGGCCAGG | 55666 |
rs181532079 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558940 | CCCTCCCTGTGCGCC[C/T]CAATTCCAGGTGCCA | 55666 |
rs181622334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620421 | GAAATGCTTGAACCC[G/T]GGAGGCAGAGGTTGC | 55666 |
rs181694884 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580404 | TCCAGCTCCGAGCCC[A/T]GCAGCCAGAGTGATC | 55666 |
rs181836102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575193 | CAAGCTCCGCCTCCC[A/G]GGTTCAAGCCATTCT | 55666 |
rs181846294 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597812 | AAAAATTAGCTGGGC[A/G]TGGCCGGGTGTGGTG | 55666 |
rs181858889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615538 | CTAAAGAAAGTAGAG[C/G]AAATCCCCAGGGGAC | 55666 |
rs181873860 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637261 | GAGATTACTTCTGCT[A/C]GTCCTCGGAAACCCA | 55666 |
rs181971075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622437 | CTTTTAAAGAAATTT[A/G]TACTGTTCACAAAGG | 55666 |
rs181973654 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581458 | CTTGTCCTCAAGAGG[C/T]TCCCTCAAACCCAAT | 55666 |
rs181976413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603072 | CACTTGGGAGGCTGA[C/G]GCAGGAGGATTGCTT | 55666 |
rs182030781 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559620 | GCCTCCTGCACCACA[C/G]GGAGTAACAGGGAGC | 55666 |
rs182079540 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586001 | TTCAAAAGAAAAATA[A/C/T]AGGTCAGGCACAGTG | 55666 |
rs182254766 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611613 | CCTCAGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 55666 |
rs182267912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568964 | ACAATACTGACACTA[G/T]ATAACAATCAGCAGT | 55666 |
rs182330778 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609253 | TCAAACTCCTGACCT[A/C]ATGATCCACCCGCCT | 55666 |
rs182373396 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566682 | TGACAGAGAAAGGCC[G/T]GGGGAGGAGGAGCCT | 55666 |
rs182389838 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607666 | GCCCCCACTAGAGAC[G/T]GTGTTCCTTGACCTA | 55666 |
rs182392667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564882 | AGCATTTGTCCAGGG[C/T]CGTAGCTCCCGGGCA | 55666 |
rs182444447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630947 | GGAGGCCAATGCGGG[A/C]AGATCACCTGAGGTC | 55666 |
rs182445794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613592 | CAAATGCCAACCACC[C/T]CTGTAGGCCTAAACA | 55666 |
rs182446836 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583151 | TGACTTTTCAGTGAG[A/C]GACTTGGAAATATCT | 55666 |
rs182455183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605145 | CCAGAGCCAGGCGTG[A/G]TGGCGGGCGCCTGTA | 55666 |
rs182459574 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560239 | CCTGGCCAACATGGC[A/G]AAACCCGGTCTCTAC | 55666 |
rs182516055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591748 | AGTTAACTATCATTC[A/C]CTTCACAAATCAGTC | 55666 |
rs182575031 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586463 | AAAAACACAAAAAAT[C/T]AGCCGGGCAGGTGGC | 55666 |
rs182593585 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565896 | GAGCTCATGCCTCTC[A/G/T]TCCTGGAGGCTGGGA | 55666 |
rs182593954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626722 | AGGATCGTTTGAGCC[C/T]GGGAAGTCAAGGCTG | 55666 |
rs182605661 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608079 | CCTTTCTGGCCACTG[G/T]TACCACCTCTGCCCA | 55666 |
rs182643475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587291 | TCAACCTGGCCAACA[C/T]AGTGACACCCTGTCT | 55666 |
rs182897708 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593414 | GAGTCAGTCCAGAAG[C/T]ACTGACACACCTAAA | 55666 |
rs182915996 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623614 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 55666 |
rs183014241 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618044 | TGCCTTGGCCTCCCA[A/G]AGTGCCGAGACTGCA | 55666 |
rs183102866 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577666 | AACCGTCTGTCCTGC[A/T]CCATCTTCAAACTCT | 55666 |
rs183180319 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572709 | GCCTGGCACTCAGGC[A/G]CGATCTGCGACAGGC | 55666 |
rs183181924 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613938 | TTCTCGGCGTTCACA[G/T]ACACACGTAAGCACA | 55666 |
rs183185105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594354 | ATGTATTAATTATTA[A/G]CATAATTAACGTGTG | 55666 |
rs183196458 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633959 | GCAATCTCCGCCTCC[C/T]GGGTTCTAACTTTTC | 55666 |
rs183241396 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605375 | AAACCAGTCAGGCAC[A/G]GTGGCTCATGCCTGT | 55666 |
rs183257865 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571273 | GGAAATGAGCCGCCT[C/T]CCGTCCGCTTTGGAC | 55666 |
rs183258641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559710 | CCCCGGGGGATGTGC[A/G]TTTGGGTTGTTTCCA | 55666 |
rs183261175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604159 | TCTGGTGATTGGTGC[C/T]GAGGTGTGTCTGTGG | 55666 |
rs183291385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599399 | TAGGTCAAAAAATTG[A/G]ACCAATCTCTTTTAA | 55666 |
rs183303054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576415 | GGAAACTCATGTATA[C/T]GGAGGTCTAACTTTA | 55666 |
rs183314245 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638668 | GTGTTGATTGGTTGG[C/G]TCAGAGGTGAAATGA | 55666 |
rs183323351 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557944 | CAAGAATGTGGGTCA[C/T]GTGGGCTTACCCCCC | 55666 |
rs183349256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600231 | TGACCTTGTGCAGCC[A/G]GAGAGAGCCAGTACC | 55666 |
rs183354645 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557501 | GAGGAACTGGCAACG[C/T]GGCTCTCTCTAGAAG | 55666 |
rs183507096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582064 | AAAGAACACCCGAGG[A/G]GCCCAGACACCACAG | 55666 |
rs183754043 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578899 | CATAATAAACATACA[A/T]TTCATTTCATATTTA | 55666 |
rs183765763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601224 | AAAGGTAATCTCAAA[C/T]TGAGTTACAGTAACT | 55666 |
rs183766166 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558511 | CCCTGGACACAACCT[C/T]GGGGGCTTCACTAAA | 55666 |
rs183808013 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587965 | CAGGCATGAGCCGCC[A/G]CGCCCGGCCGAAAAA | 55666 |
rs183810803 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628075 | AAATTAGCCAGGCAT[A/G]GTGGTGGGCGCCTGT | 55666 |
rs183818083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622627 | ATGATCTCGGCTTAC[C/T]GCAACCTCCACATCC | 55666 |
rs183892216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630593 | TCCCTAAAAAACGTT[C/T]AAAAATGGCCAGACA | 55666 |
rs183940276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571719 | AGAGGCTGCCTAGCC[C/T]GGGGTCAGTGGTCCT | 55666 |
rs183965029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567633 | AACTCAATACACTGA[A/T]TGCTGAGACACCTCT | 55666 |
rs183982368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609545 | CAATTCCTAGGCTCA[A/G]ATGATCCTCTGGCCC | 55666 |
rs183991953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613707 | TCTCTGTAATTTAAT[C/G]TCTTACAACTTTACC | 55666 |
rs184020866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634799 | CATGTTGGTCAGGCC[A/G]GTCTTGAACTCCTGA | 55666 |
rs184031734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624492 | CAGTCCCAGCTAGTC[A/G]GTGGGCTGAGACAGG | 55666 |
rs184038729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584974 | CAGGAGTTCATGACC[A/G]GCCTGGGCAACATGG | 55666 |
rs184040828 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606513 | ATCTCCAAGAGCAAG[A/C]AGCCTTAAAAATGAT | 55666 |
rs184100869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563828 | TGGATGCAGTTGAAG[A/G]CCATTATTCTAAGCA | 55666 |
rs184125893 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585660 | AGGAAGACTCCATTT[C/T]TGGGGGGGGGGGGAA | 55666 |
rs184130861 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633655 | AAAATAAGACTAGAA[C/G]GCTTCTTGGGGAAGT | 55666 |
rs184148568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593974 | CCAAGCAACAACTTA[A/G]GAAAATAAATCTGAC | 55666 |
rs184193604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588544 | GTAGAGACACAGTCT[A/C]GCTATGTTGCCCAGG | 55666 |
rs184193761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609951 | TGTCCAGGGAGCCCG[C/T]TGTAAATGCTGCCCC | 55666 |
rs184207192 | snp | A/G | 0.0139171 | 0.0822489 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629675 | TATCGATGGCAGTAA[A/G]AGTAGAGGATGAAAA | 55666 |
rs184255482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567953 | GCTTGGTGGCGCGCA[C/T]CTATAATCCCAGCTA | 55666 |
rs184425316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615565 | GGACAAACCCAGCAG[G/T]GCACTCAGACAGCAG | 55666 |
rs184442515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637417 | CACAGGTAAGTAGAG[A/G]AACAATTTCAGGAAG | 55666 |
rs184494070 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575345 | TGACCTCATGATCCA[C/T]CCGCCTTGGCCTCCC | 55666 |
rs184500998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598591 | GAAGGAAGCATCTGA[A/G]GGTATGAGGATCTGA | 55666 |
rs184541208 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610536 | CACCTCAGCCTCCCC[A/G]AGTATCTGGGACTCC | 55666 |
rs184541340 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568601 | CCAACACGGGAGCCA[C/G/T]GCTAAGCAGCAGATC | 55666 |
rs184565223 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619733 | AAAATACAAAAATTA[C/T]CTGGGAATGGTGGTG | 55666 |
rs184573726 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602118 | AAAAATGTCACATAC[A/C]AAAAAAACAAAACTA | 55666 |
rs184640099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580068 | ATGCTCCTGCCCCTC[C/T]TCCCCAGCTCCTGCC | 55666 |
rs184658225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590025 | CTGGAGGCAGAGAGA[C/T]GGGGAAGCGGGTGGG | 55666 |
rs184664525 | snp | A/G | 0.133093 | 0.220981 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618098 | TCTGGGAAGTGAGGA[A/G]CCTCTCTGCCTGGCC | 55666 |
rs184675277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595161 | TCAACCTCCCAAAAT[G/T]CTATGATTACAGATG | 55666 |
rs184729596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574808 | GGCTTGAGGTCGGGA[A/G]TTTGAGACCAGACTG | 55666 |
rs184774985 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583553 | CCCAGAGATGAGTGA[A/G]GCTGGCTGGCCCTAG | 55666 |
rs184779854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580539 | CCAGCAGGCCACCCT[C/G]CTTATCACTCTCTGT | 55666 |
rs184824227 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620689 | TTAAAAAGAGGAGGG[A/T]GAAAAAAAGGCCAAG | 55666 |
rs184824512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614661 | CTTTCAGTCTGAAGT[C/G]TGTTCTTCCCTTGGT | 55666 |
rs184827017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573495 | ATTAAATTCTGGCTG[A/G]TCCGAAGGTGGTGAG | 55666 |
rs184885512 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559040 | TGCGTTTCCAGTCTG[C/G]AGACTGCATTCAGCC | 55666 |
rs184914312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602349 | GCCAGGAGTTTGAGA[C/T]CAGCGTGGGCCACAC | 55666 |
rs185269895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626865 | GAGGCTGAGGCGGGC[A/G]GATCACCTGAGATCA | 55666 |
rs185276000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624955 | GGAAGCCACACAGAC[A/G]AAAGGCAGGGGGAAT | 55666 |
rs185276724 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608361 | TCTGTCTGATACTGC[A/G]CTGTGGCCACGCAGC | 55666 |
rs185277471 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575933 | GCTGGAAGCAAACAC[A/C]ATCTCCTATGAGTGA | 55666 |
rs185285168 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598961 | GTAAATAAAGCAAAA[G/T]CAAAATCAAACTGAG | 55666 |
rs185322187 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562402 | AAATTAGCTGGGTGT[C/G]GTGGCAGCCACCTGT | 55666 |
rs185346351 | snp | A/G | 0.486529 | 0.0809556 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605819 | GCAAAAAACAAACAC[A/G]TTTTCTTTTTTTTTT | 55666 |
rs185350904 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586558 | GAGGCTGCAGTGGGC[C/T]GAGATCGCGCCACTG | 55666 |
rs185364541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565939 | GTCTTGACTGTGAGA[C/T]GTGTCCTCCTCCCTC | 55666 |
rs185411093 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602860 | GCCTGGGTAACATGG[C/T]GAGATCTGTCTCCAC | 55666 |
rs185425158 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581262 | GAGGCTGAGGCAGGA[C/T]TGCTTGAACCTGGGA | 55666 |
rs185429284 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621176 | CAAAACCCCTCACCA[C/G]CTCAAAAGAAGGATG | 55666 |
rs185433750 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631127 | GCAGTGAGCCAAGAT[C/G]GTGCCATTGCGTGAC | 55666 |
rs185475763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583814 | CTTCTACTCCCACCC[C/T]ATGTGTGAGTGCATG | 55666 |
rs185482498 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624195 | GGAGGCCGAGGTGGG[C/T]GGATCACGAGGTCAG | 55666 |
rs185495039 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81559284 | GGGAGGCTGCACATC[C/T]CGCAGTGGCCTGTGC | 55666 |
rs185495778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571007 | GGTTTTAAATCATGC[C/T]TGCTCCTCCTGGGTG | 55666 |
rs185506505 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558915 | AAGGCTGGGTGGTGG[C/T]AGCATCGGCCCCTCC | 55666 |
rs185507330 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593138 | CACTACTTACAATGA[A/T]ATGAGATTAGAAGCA | 55666 |
rs185585767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615370 | CTCCCAAAGTGCTAG[A/G]ATTACAGTCGTGAGC | 55666 |
rs185693965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596675 | TCTAAAACCACTCAC[A/G]ACTAGAAAGGCCAGA | 55666 |
rs185713774 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635204 | AGACATCAGCCATGC[A/G]TGTTGGCGAGCACCT | 55666 |
rs185783134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561972 | GTCTTGTGTATACAC[A/G]TCTGTAATCCCAGCA | 55666 |
rs185824896 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612990 | CTCTGCACGGGAATC[A/G]GCATCTCCAGGGGAC | 55666 |
rs185843152 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631405 | GTGTGTGTGCATATA[C/T]GCATATTAAAGTGTA | 55666 |
rs185924972 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616761 | GTAACACACTACCAC[A/G]CAAGTAAGAGTGGGC | 55666 |
rs186070702 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638189 | GACAGGGGAATTGCA[A/G]TAAAGAGTTTAATTC | 55666 |
rs186079950 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613596 | TGCCAACCACCCCTG[A/T]AGGCCTAAACAATGA | 55666 |
rs186130003 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569276 | TATCTATTAGTGTCA[C/T]CTCTAAACGAACACT | 55666 |
rs186223809 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593722 | GACACTTTTCTCCCC[A/G]TCTCTAAATACAACG | 55666 |
rs186224446 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556735 | AAGGTTGGGAGGGAT[C/T]GGCTGGGGAAGTGGG | 55666 |
rs186226080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631987 | TTTTTTTTGAGACAG[C/T]CTTTTTCCGTTGCCC | 55666 |
rs186241122 | snp | C/T | 0.139564 | 0.224285 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637619 | GCCTGGCCAAAATGG[C/T]GAAACCCCGTCTCTA | 55666 |
rs186245154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598878 | ACTGTCTTTAAAGAT[A/G]CCCCAATGAATGAAA | 55666 |
rs186290331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622536 | TTTAAGACTTTGAAG[C/T]AAACAAGAGTTAATG | 55666 |
rs186354595 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603417 | CCTGGGCAATATAGC[A/G]AGACCCTGACTCTAC | 55666 |
rs186360051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575574 | TCCAAGACAGGAAGG[A/G]TTACAAAGATGAGTG | 55666 |
rs186460346 | snp | C/G | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557363 | TCGCCAATGCTTTTC[C/G]TTTAGCTAAAAGACA | 55666 |
rs186470754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607155 | CCTGTGCCACTGAGC[A/G]GGCATGAGGCTCCTA | 55666 |
rs186633626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578906 | AACATACATTTCATT[C/T]CATATTTAAAATGTT | 55666 |
rs186642137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601291 | CCACAAAGAAGTTTA[C/T]GTTTGCTGGGTATTA | 55666 |
rs186646611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627511 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACCTGAG | 55666 |
rs186648163 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558569 | TCTCACTCCCCTTTT[C/G]TGCAGTTTTTATCTT | 55666 |
rs186705370 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605219 | CCGGGAGGTGGAGCT[C/T]GCAGTGAGCTGAGAT | 55666 |
rs186740521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622924 | TCCAGGCCAGGCGTG[A/G]TGGCTCATGCCTGTA | 55666 |
rs186769504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583217 | TATTTTGAAGATATA[C/T]AAAGATGTCACAGGA | 55666 |
rs186779380 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561009 | GTTGCCGAGGCTGGA[A/G]TGCAATGGCGCAATC | 55666 |
rs186890599 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607889 | AATATGACATCCTTC[A/T]CAAAATGTTGCTGAC | 55666 |
rs186896572 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565172 | TCCCACGCTTCCGGC[G/T]CTTCCATAAAGTTTC | 55666 |
rs187037026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592093 | GGGAAAGGGGAGGAA[A/G]GACAGATGCAGAGGG | 55666 |
rs187044467 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559689 | CTCCTTGTGAATAAC[A/G]TAACTCCCCGGGGGA | 55666 |
rs187102823 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625488 | CAAATCATAAAAGAA[C/T]AATCAAATGGAAATT | 55666 |
rs187262050 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611699 | GTGTGGTGGCTTGCG[C/T]CCTGTAATCCCAGCA | 55666 |
rs187266806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581508 | CAGAGGAATAAGCCC[C/T]GTGGACGCCCAGACC | 55666 |
rs187431659 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564806 | AAAAAAAAAAAAAAA[C/G]AGGAAATGGTATAAA | 55666 |
rs187442699 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634338 | TTTCTTAAATTCAAA[A/G]TAACTTTTTAAATCA | 55666 |
rs187507723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573130 | TTCATTAAAGATTCT[C/G]CAAGAGGGGATCACA | 55666 |
rs187510360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614043 | GCACTTTGGGAGGCT[A/G]AGGCAGATGGATCAC | 55666 |
rs187516014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594444 | TAAATCAAGGAACTG[A/C]AGGCTGGGCAACACA | 55666 |
rs187554703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638916 | CCATAATTTCTAATC[C/T]TATGGCTAATTTGTT | 55666 |
rs187583899 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624007 | ACAAGGTTTCTGGCC[A/G]GGCGTGGTGGCTCAT | 55666 |
rs187621323 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599563 | AGTCACATTTGCAGT[C/G]TCACCCGCTTCATCT | 55666 |
rs187625037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567740 | TCCCAAGAAGATGCT[C/T]TCAGCACACCTGACT | 55666 |
rs187630699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616970 | AAGTCAGTGGCTCTT[C/T]CCAAATCTCCCTCCT | 55666 |
rs187637094 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577110 | CAATGCCTGGCCACA[C/G]CAAGGGGCAGTGGGT | 55666 |
rs187668530 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614975 | CCAAAGTGCAGGCCC[C/T]CAAGGACACACAGAC | 55666 |
rs187783096 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571852 | CACCGCATGCTCAGT[G/T]ATTCTACAACCACCT | 55666 |
rs187790602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600960 | GAACTCCACAGAGAG[C/T]GATGAGCTCACCAAC | 55666 |
rs187798754 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558079 | ATGCCCACCACTCCC[C/T]GGGTAAGAGCCATGC | 55666 |
rs187823167 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566829 | AGTCGGACCCCTACA[C/T]ACGGCAAGAACCTCC | 55666 |
rs187847155 | snp | C/G/T | 0.00398731 | 0.0445001 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609264 | ACCTCATGATCCACC[C/G/T]GCCTTGGCCTCCCAA | 55666 |
rs187919111 | snp | C/T | 1.65839e-05 | 0.00287953 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596239 | AACTTAGGAAATAGG[C/T]GTCCTAAGACAAGAG | 55666 |
rs187947149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634860 | AGTGCTGGGATTACA[A/G]GCGTGAGCCACTGCA | 55666 |
rs188086520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578359 | CCTGCTCCCCAACAG[G/T]ACACCTCCACAGTTT | 55666 |
rs188098312 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618047 | CTTGGCCTCCCAAAG[A/T]GCCGAGACTGCAGCC | 55666 |
rs188226171 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621567 | TGGGAGCCAGCACCC[A/G/T]TGTTCCGTAAAGGAC | 55666 |
rs188329660 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582212 | GGCTGCAGCAGCACA[A/T]CCAGGAGGGCCGTGA | 55666 |
rs188345684 | snp | C/G | | | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81564105 | ACACACACACACACA[C/G]ACACACACACACAAA | 55666 |
rs188372646 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624796 | TAAGCCCGCCACACG[C/T]GAGCTGGGAGAAAAG | 55666 |
rs188378584 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585030 | AAAAAATCAGCCAGG[C/T]GTGGCAGCGTGCGCC | 55666 |
rs188378896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606540 | TGATATATTCAGTGT[A/G]CCACTTCCACAAAAG | 55666 |
rs188450628 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609802 | ATTAACAGTTCCAGT[A/C/T]GGCATTATTACGGTA | 55666 |
rs188519228 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568183 | TGCGGGAGGGGCCTG[A/G]GGCCCCCTTCACGGC | 55666 |
rs188523368 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610038 | CCATAAATAAAGGCT[C/T]GTCCTGTGTGCAGCT | 55666 |
rs188525543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588632 | GGATTACAGGCATGA[C/G]CCACCATGCCAAGGA | 55666 |
rs188579055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562041 | GAGTTCCAGACCAGC[C/T]TGACCAACATGGTGA | 55666 |
rs188593753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633670 | CGCTTCTTGGGGAAG[C/T]TGAAGAACTGGTGAG | 55666 |
rs188608363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605729 | AGGAGGATGGAGATG[A/G]GTTTCATCTATCAAT | 55666 |
rs188626924 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604225 | TGGTGGAAGAGACAC[A/C]GAATGACACAAGGAC | 55666 |
rs188629004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560046 | AGCCTCCAGTTTTGA[A/G]CTAATATGAACAAAG | 55666 |
rs188723553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628462 | AGGTTGCAGTGAGCC[A/G]AGATCATGCCACTGC | 55666 |
rs188725769 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588274 | AGCCCCCAAAGGAGC[A/G]GGAAACACCAAAAAG | 55666 |
rs188765197 | snp | A/T | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557552 | CCCAGTGGTGGGGGA[A/T]GGCCTTGGACTCACA | 55666 |
rs188836416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630374 | CTTACTGCAGCCTTG[A/G]CATCCAAGGTTCAAG | 55666 |
rs188868225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583679 | AATCACTTCTCCAAG[A/G]CCAGCATCTGCACAG | 55666 |
rs188878377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613823 | CTCCCGCCTCTCACC[A/C]TCTGCTTGGCCCCCA | 55666 |
rs188879128 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598653 | GTGTAGCAGTGCCTG[G/T]GTGCTGTGTGATCCT | 55666 |
rs188886543 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637526 | ATTTCAGGCCGGGCG[C/T]GGTGGCTCATACCTG | 55666 |
rs189018009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592399 | TCGGCCACCACCCTC[A/G]GGAAAGGGAGACCAT | 55666 |
rs189020004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602197 | AGGTAAGAGGATCTC[A/G]CTCAGGAGCGAGACC | 55666 |
rs189034114 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569827 | CTAAGATATAATCAA[C/T]AGATGCTACAGGGAC | 55666 |
rs189051309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563464 | ACTCCTAGGTACTCC[A/G]AAAGCTGATGCAGGA | 55666 |
rs189075021 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590416 | GGGCAGCCTGAGCCT[C/T]TGGAGGAGGCAGGCA | 55666 |
rs189102714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630700 | AGTGGGCAACATGGG[A/G]AAACCCCATCTCTAC | 55666 |
rs189159331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574967 | TTGAATGGCATCAAC[C/T]CTGCTTTAGAAAAGG | 55666 |
rs189166164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597102 | TGGGCAAAAGAGCAA[A/G]ACTCCGTCTCAAAAA | 55666 |
rs189239900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573936 | CCTCCTTCCACGTGA[C/T]GAGTGGCTGCCAGTC | 55666 |
rs189371173 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610618 | GAAAAAACTGACCCG[C/T]ACATCAAACCTGTGA | 55666 |
rs189371295 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568655 | GGCCAGGCCGAGAGG[A/G]GCCACACAGCCCCAA | 55666 |
rs189401802 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559126 | CAGTGGGTCAGGGAG[C/T]CCAGGACAGCCAGCC | 55666 |
rs189477785 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615458 | ATCTAACTACTAATA[C/T]AAAAAACTTGACTTA | 55666 |
rs189687475 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580888 | CAGCTCTCGCTCCCC[A/G]CTCAGCTCTGAAGGG | 55666 |
rs189714626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566326 | AACAGAGCGAGACTC[C/T]GTCTTAAAAAAAAAT | 55666 |
rs189720695 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587280 | GGAGTTCAAGATCAA[A/C]CTGGCCAACATAGTG | 55666 |
rs189746103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608587 | ATAAATAAATAAATA[C/T]AGAACCACGGTAACT | 55666 |
rs189746976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602354 | GAGTTTGAGACCAGC[A/G]TGGGCCACACAGAGA | 55666 |
rs189755769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559606 | GCCCTCAGAAAAATG[C/T]CTCCTGCACCACAGG | 55666 |
rs189760528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626961 | TGGGCATGGTGGTGC[A/G]AGCCTGTAGTCCCAG | 55666 |
rs189788477 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581335 | GCCTGGGCAACACAG[C/G]CAGACTCCAACGCAA | 55666 |
rs189797172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602900 | ATATGTATATACACA[C/T]ACATACATATATATG | 55666 |
rs189903791 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584150 | ATGTCACCTCCAACC[A/G]CAAAGTCCATGGGAG | 55666 |
rs189997332 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612429 | AGCCAGTGCCAGGCC[C/G]CTGGGAGGAGACACA | 55666 |
rs190012432 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620810 | CACAGTCATTCTCTT[C/T]ACCTTTAGATAATGG | 55666 |
rs190044522 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580321 | CCTGCCTCTTCTCTC[A/G]ATCACACCACACACT | 55666 |
rs190143887 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605904 | TTGGCTCACTGCAAC[C/T]TCTGCCTTCAGGTTC | 55666 |
rs190145753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575500 | ATTTCTCAGGGGCCA[A/G]CTGTGTGCACAGAGC | 55666 |
rs190242899 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631128 | CAGTGAGCCAAGATC[A/G]TGCCATTGCGTGACG | 55666 |
rs190254169 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571206 | TGCCTGAATCACGTG[C/T]CCATCCAATTTCAAA | 55666 |
rs190264855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593376 | CACACAGGCCAGTAC[A/G]GATCCTGCTGTGCTG | 55666 |
rs190285567 | snp | A/G/T | 0.000198795 | 0.00996797 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613350 | TCTGTAAATCTTCCC[A/G/T]TCCTGTTTGCTGAGG | 55666 |
rs190294186 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560158 | TGCAGTGGGTCACGC[C/T]TGTAATCCCAGCACT | 55666 |
rs190299874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631536 | TACTTTCTAAGACAA[C/T]TTGATGTTTATGCTG | 55666 |
rs190310964 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558932 | GCATCGGCCCCTCCC[C/T]GTGCGCCCCAATTCC | 55666 |
rs190428184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586458 | CTACTAAAAACACAA[A/T]AAATTAGCCGGGCAG | 55666 |
rs190443455 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565669 | AGCAGCTTCCTGCTA[C/G/T]AACAGGTTTCTTTCT | 55666 |
rs190503355 | snp | A/G | 0.127944 | 0.218179 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617739 | TACTGCTGCCATCTC[A/G]GCTCACTGCAACCTC | 55666 |
rs190548708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564854 | TTGAAGGCTGTGTTA[A/G]CAGAAGGATTCTAGC | 55666 |
rs190552040 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607330 | TGAAGACTGTCAATG[A/G]GAAAATCCTGGACCC | 55666 |
rs190649486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593883 | CAGGGTGCCCTAACA[C/G]GTTCTGTAATGCAGA | 55666 |
rs190651812 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632538 | AGGCTGGTCTCGAAC[A/T]CCTGACCTCAAGTTA | 55666 |
rs190674972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622564 | ATGGCTATCCTTGTT[G/T]TGTTTTCAGACAGTC | 55666 |
rs190681325 | snp | A/C/G | 0.00279258 | 0.0372817 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613931 | CACTGCTTTCTCGGC[A/C/G]TTCACATACACACGT | 55666 |
rs190802132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616407 | GGTCAAATATAACCT[C/G]TCATAAGAACCAAAA | 55666 |
rs190809559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585737 | AGCATCTATAATCCC[A/G]GCACTGTGGGAGGCT | 55666 |
rs190817760 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625245 | ACCTGTGCAGGGACC[A/C]TGAAAGGAAAGGCTA | 55666 |
rs190864950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575629 | ACAGCTGGACAGCTG[G/T]GTAGAGACTGGGCCC | 55666 |
rs190886822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613630 | TTCTAACTTTTAAGA[C/T]GAGAATTCTCTTCTA | 55666 |
rs190966681 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571538 | GGACCACCCTGGACG[C/G]AGTGACCCAGACACA | 55666 |
rs190998001 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633922 | CCCAGGCTGGAGTGC[A/G]GTGGTGCGATCTCGG | 55666 |
rs191043644 | snp | C/G | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637839 | CTCGGGAGTCTGAGG[C/G]CGGAGAATCTCTTGA | 55666 |
rs191047722 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598913 | CAAGGTGGTGGCAAC[A/G]GAGAAAATGAAACTT | 55666 |
rs191105620 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81556897 | GGCAGTTGCTTCAGG[C/T]GCTTTTATTAGGTTC | 55666 |
rs191140294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638356 | CACACTGGAGTGCAG[C/T]GGCGCGATCTCGGCT | 55666 |
rs191141170 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583535 | GTCCTGCCACCTGGC[G/T]GCCCCAGAGATGAGT | 55666 |
rs191155161 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561156 | TAGAGATGGGTTTTC[A/G]CCATGTTGGCCTGGC | 55666 |
rs191159208 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623665 | TAGCCGGGCGTGGTG[A/G]TGGGCGCCTGCAGTC | 55666 |
rs191166558 | snp | A/T | 0.143622 | 0.226238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605290 | CATCTCAAAAAAAAA[A/T]AATAAATAATAATAA | 55666 |
rs191188572 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557489 | GAGCGAGTGGGAGAG[A/G]AACTGGCAACGCGGC | 55666 |
rs191218054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576054 | TAACAACAAAGGAAT[A/G]GATTGTAGGTAAGTG | 55666 |
rs191221972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616900 | AGAGGGTGAGTGACA[A/G]AGGCTATCCAAAATG | 55666 |
rs191225756 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599265 | CTGCACTCCAGCCTG[A/G]GTGAAAGAGCAAGAC | 55666 |
rs191318329 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558103 | GCCATGCCCCGGCCT[A/G]GCCACGCCACAGAGG | 55666 |
rs191371749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604328 | AGTGGCAAATGTACC[A/G]GTTGTGTAAGAAAAT | 55666 |
rs191433251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599755 | AGATAAACCAGATCA[A/G]TAGAATAAAAAAGGA | 55666 |
rs191437405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625935 | GGGCAGATCACCTGA[A/G]GTCAGGAGTTTGAGA | 55666 |
rs191525716 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623245 | GGGAGGCCAAAGCAG[A/G]TGGATCACGAGGCCA | 55666 |
rs191601089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582283 | CTGAAGATGCCTGCA[C/T]GTCACATCCGTACCA | 55666 |
rs191603523 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581591 | GCCAGTCCTCCACAG[A/C]ACCAAGGCCACCTCT | 55666 |
rs191695492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607934 | CATCTCCTCGTTGCA[A/C]TGACAGGAATTATAA | 55666 |
rs191702991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577541 | TCTCCCTCTGAACCA[C/T]GGCTTGGCTCATCTA | 55666 |
rs191753906 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610053 | CGTCCTGTGTGCAGC[C/T]TGCACTAGGGGAATA | 55666 |
rs191759168 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588763 | AGAAGCCCTACGCCA[C/T]GGAAGCATGAGTAGC | 55666 |
rs191766811 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630415 | ACCTCAGCCTCCCGA[A/G]AGCTGGAACCACAGG | 55666 |
rs191862577 | snp | A/C/G | 0.00279242 | 0.0372774 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594934 | GTGACAGAGCAAGAA[A/C/G]ATGTCTCAAAACAAA | 55666 |
rs191873598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614509 | CCCAAAAAGGCCCAC[A/G]GACAGACGTCCCTGT | 55666 |
rs191881831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606372 | TCAGAGCTGGTCCAA[G/T]GGGTGCCCCTTTACC | 55666 |
rs191887780 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559699 | ATAACGTAACTCCCC[A/G]GGGGATGTGCATTTG | 55666 |
rs191889674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634747 | CATGCCACCACACCC[A/G]GCTAATTTTTTATTT | 55666 |
rs191891260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603587 | GGCAACAGAGCAAGA[C/T]TCATCTCTAAAAAAT | 55666 |
rs191893621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584691 | ATACTGAGGAACAGA[C/T]AGCAGTTGCTGGATA | 55666 |
rs192016591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567904 | AACATGGCGAAACCC[C/T]GTCTCTACTAAAAAT | 55666 |
rs192050385 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588359 | CTCCCACGGTCTTCT[C/T]ATCTCCACCCCTATC | 55666 |
rs192053881 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609925 | AGCTTTGTGTCAGAT[C/T]GGAAAAGGATTGTCC | 55666 |
rs192136176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635126 | GCGGGCGGATCACGA[A/G]GTCAGAAGTTCGAGA | 55666 |
rs192165779 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572412 | TTGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 55666 |
rs192201287 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594254 | CAGTCCAGCCTGGGC[A/G]AAAGAGCGAGACTCC | 55666 |
rs192205778 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596598 | AAATAAGAACCAAAC[C/T]ATAAAACTCAAAACC | 55666 |
rs192372149 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578767 | TCATCTCTCCTTGAC[A/G]CCTGGGGATTGTGAG | 55666 |
rs192525061 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615222 | CTCCTGCCTCAGCCT[A/C]CCAAGTAGCTGGGAT | 55666 |
rs192608548 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579899 | CCTCTGTGAGCTCAC[C/T]CCCCATTCTCCTCTG | 55666 |
rs192624898 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558702 | AGGGCAGGCAGCAAA[C/T]CGACCTGCAGACCTG | 55666 |
rs192630693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574678 | CGCCAAGGTCTTGAC[A/C]CCAAGAGAAATCCAG | 55666 |
rs192634894 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619307 | GCATGAACCCGGGAG[A/G]TGGAGCTTGCAGTGA | 55666 |
rs192640799 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601743 | AAGAACCATGGCAAA[A/G]GCCTCATGAAACACT | 55666 |
rs192675445 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618074 | AGCCTCTGCCCGGCC[A/G]CCACCCCGTCTGGGA | 55666 |
rs192725343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600963 | CTCCACAGAGAGCGA[G/T]GAGCTCACCAACCCT | 55666 |
rs192763821 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573371 | TCAGGAAGCCCCGCT[A/G]TCTTCTGAGACAATC | 55666 |
rs192849117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629610 | AGAAAGGCAATGCAA[A/G]AGGCAATTTGGGAAT | 55666 |
rs192895118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568187 | GGAGGGGCCTGGGGC[A/C]CCCTTCACGGCAGGG | 55666 |
rs192921690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583761 | TGGGACAGGGCAAAG[C/T]TGTAGACTCTCCTCC | 55666 |
rs192983390 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624379 | GCCAAGATGGCGCCA[A/C/T]TGCACTCCAGCCTGG | 55666 |
rs193087023 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624036 | ATGTCTGCAATCCCA[C/G]CACTTCGGGAGGCCA | 55666 |
rs193125628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609451 | AGCTGGGACTACAGG[C/T]GTGAACCACCACACC | 55666 |
rs193146859 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567129 | AGCTAAATCACCTCT[A/C/G]CTTCCCATTCGATTG | 55666 |
rs193242314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605739 | AGATGGGTTTCATCT[A/G]TCAATAAATTCAAAA | 55666 |
rs193281559 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587566 | GTGATCCGCCCGCCT[C/G]AGCCTCCGAAAGGGC | 55666 |
rs193282318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627745 | CACACTCCAGCCTGG[A/G]CAACAAGAGCGAAAC | 55666 |
rs199493375 | in-del | -/AT/CG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605819 | GGCAAAAAACAAACA[-/AT/CG]TTTTCTTTTTTTTTT | 55666 |
rs199493377 | in-del | -/AA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616743 | TCTCAAAAAAAAAAA[-/AA]GAGTAACACACTACC | 55666 |
rs199514365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587077 | GGAAAACACATTGCA[A/G]CTGCAGACCCACATA | 55666 |
rs199525508 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559697 | GAATAACGTAACTCC[C/T]CGGGGGATGTGCATT | 55666 |
rs199530403 | in-del | -/AT | 0.00478085 | 0.0486577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602965 | CATATATATACACAC[-/AT]ATATATACACAAATA | 55666 |
rs199544246 | snp | C/T | 3.31647e-05 | 0.00407201 | synonymous-codon, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81589019 | CGGGGCGTCCTTGCA[C/T]GGCAGCAAACACTCA | 55666 |
rs199549512 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631466 | TTTTTTTTTTTTCCC[C/T]CACGGCAAGCCTAAA | 55666 |
rs199554826 | in-del | -/AACG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594948 | ACATGTCTCAAAACA[-/AACG]AACAAACAAAAAAAA | 55666 |
rs199574232 | snp | C/T | 0.153 | 0.230415 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602944 | ACACATATATATATA[C/T]ACACACATATATATA | 55666 |
rs199616089 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610977 | AAAAAAAAAAAAAAA[A/T]AAAATGACACAAACC | 55666 |
rs199622756 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632255 | GCTGGGATTATAGGC[A/T]TGAGCCACCAACCCT | 55666 |
rs199626420 | snp | C/T | 0.000314666 | 0.0125393 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596192 | GTTGGGATGCTTGTT[C/T]TGGAAGTCTCCTGCA | 55666 |
rs199657473 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636514 | AGGAGAGAATCAGAG[A/G]GAGATTAGGATAAGA | 55666 |
rs199678879 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586608 | GAGCAAAACTGTCTC[-/A]AAAAAAAAAAAAAAA | 55666 |
rs199688182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628651 | GTCTGAAGAGAAACA[A/C]CACCAGACAGAAATA | 55666 |
rs199791293 | snp | A/G | 0.000874027 | 0.0208866 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81559286 | GAGGCTGCACATCTC[A/G]CAGTGGCCTGTGCCT | 55666 |
rs199815714 | in-del | -/AAAA | 0.158302 | 0.232576 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633128 | GCAAGACTCCGTCTC[-/AAAA]AAAAAAAAAAAAAGA | 55666 |
rs199850449 | snp | A/G | 0.00055229 | 0.0166084 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610176 | CCCGCAGCCCCCCAC[A/G]CTGGCCCAGAACTTA | 55666 |
rs199862664 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595535 | CATATATATATATAT[-/A]TTTTTTTTTCTTTTC | 55666 |
rs199992429 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606019 | TAGAGATGGGGTTTC[A/G]CCATATTGGCCAGGC | 55666 |
rs200007174 | snp | G/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614606 | TTAAGGGTACTGCTT[G/T]CCAAAAAGGTTGCCA | 55666 |
rs200009761 | in-del | -/AAAAAG | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635371 | TTAAAAAAAAAAAAA[-/AAAAAG]GAGTCGACGTTTCCT | 55666 |
rs200056570 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606834 | ATAGAAGAGAAGCAA[A/C]TTAAACATCACATTG | 55666 |
rs200065610 | snp | A/G/T | 0.00120019 | 0.0244674 | synonymous-codon, nc-transcript-variant, missense | NPLOC4 | GRCh38.p7 | 17:81559373 | TGTGGAGCCCCCGAC[A/G/T]GCGCCGTACTCATGG | 55666 |
rs200072788 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609434 | GCCTCAGCTTCCTGA[A/G]TAGCTGGGACTACAG | 55666 |
rs200088672 | snp | A/G | 0.000394945 | 0.0140469 | synonymous-codon, intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81608763 | CTTCCGGATGTAGGC[A/G]TGGAAGGACATGTGC | 55666 |
rs200147658 | in-del | -/GAAG | 0.0267878 | 0.112589 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621113 | AGAAAGAAAAGGAAA[-/GAAG]GAAGGAAGGAAAGAA | 55666 |
rs200161102 | snp | A/C/G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626331 | AAGAAAAAAAAAAAA[A/C/G/T]AAAAGAATGAAAATA | 55666 |
rs200188877 | snp | A/G | | | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81565599 | CTCCAGCAGCAAGCT[A/G]ATGCTGTCCTACAAG | 55666 |
rs200215584 | in-del | -/AT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595522 | CATATATACATATAC[-/AT]ATATATATATATTTT | 55666 |
rs200227739 | in-del | -/G | 0.489665 | 0.0711382 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618485 | GTCCGGGAGGAAGGT[-/G]GGGGGGTCAGCGACC | 55666 |
rs200287444 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595530 | ATATACATATATATA[-/T]TATATTTTTTTTTTC | 55666 |
rs200308004 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619895 | AAAAAAAAAAAAAGG[A/C]GGGGGTACAGCACCC | 55666 |
rs200312567 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605818 | GGCAAAAAACAAACA[-/C]ATTTTCTTTTTTTTT | 55666 |
rs200318542 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630180 | GATGTTACTTTGGGG[-/A]AAAAAAAAAAAAAAA | 55666 |
rs200329005 | snp | A/G | 0.000269675 | 0.0116088 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81572017 | ATGGGGGGCACTTAC[A/G]TCTATGATGAGATAC | 55666 |
rs200367539 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610975 | AAAAAAAAAAAAAAA[A/C]AAAAAATGACACAAA | 55666 |
rs200410384 | snp | A/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614599 | TGAAGCTACTGACGT[A/T]CTGCTTTCCAAAAAG | 55666 |
rs200426908 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638301 | GTTTTTTGTTTTTTG[-/T]TTTTTTTTTGTTTTT | 55666 |
rs200503398 | in-del | -/ATCT | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567215 | AAGGTGAAAAAATTA[-/ATCT]TTCTATCAACAAGCT | 55666 |
rs200527464 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610671 | AAATGACACAAACCA[A/G]GCCGGGCGCGGTGGC | 55666 |
rs200540726 | in-del | -/C | 0.375 | 0.216506 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623809 | TCTCAAAAAAAAAAA[-/C]AAAACTCAATTCCAA | 55666 |
rs200549665 | snp | C/G | 3.31422e-05 | 0.00407063 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622149 | CATTCCCTGCTTCCT[C/G]CTCAGAGGACACTTA | 55666 |
rs200552698 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624611 | TCAAAAAAAGAAAAA[-/C]AAAAAAAAGACAAGG | 55666 |
rs200583355 | snp | A/G | 9.96876e-05 | 0.00705931 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81569079 | CGAAATAGAAAAAGT[A/G]TAAACTGGATCCTTG | 55666 |
rs200619979 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585617 | AGTGAGCCGAGATCA[C/G/T]GCCACTGCACTCCAG | 55666 |
rs200654920 | in-del | -/AT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605292 | TCTCAAAAAAAAAAA[-/AT]AAATAATAATAATAA | 55666 |
rs200675209 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634605 | TTTTTTTTTTTTTTT[-/T]GAGACAGTCTTGCTC | 55666 |
rs200732325 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576534 | TCAACTGAGGGGCAA[C/T]TGTACTTCCAAAGTA | 55666 |
rs200745973 | in-del | -/G | 0.248755 | 0.249997 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576654 | ACGAAAACCTGGCGT[-/G]TGTTTGCAACACACG | 55666 |
rs200752877 | snp | A/G | 0.000149067 | 0.00863199 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81597266 | TCGACTGTAGCGGAC[A/G]GTACCCTTTCGGGTA | 55666 |
rs200764596 | snp | A/G | 0.00169897 | 0.0290964 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559232 | GGCTGGGCTGGGCCC[A/G]GTCCTAGCCAGCAGA | 55666 |
rs200773173 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587675 | CAAAGAAAAAAGTTG[-/T]TTTTTTTTTTTTTTT | 55666 |
rs200774748 | in-del | -/TTTC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631460 | TTTTTTTTTTTTTTT[-/TTTC]CCCCACGGCAAGCCT | 55666 |
rs200779501 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581373 | AAAAAAAAAAAAAAA[A/G]AAAGTTAATAAAATC | 55666 |
rs200781245 | in-del | -/TTTG | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638298 | CAGAGTTTTTTGTTT[-/TTTG]TTTTTTTTTGTTTTT | 55666 |
rs200820996 | snp | A/G/T | 0.000316732 | 0.0125807 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596076 | ACAAAATATATTAAC[A/G/T]AGGTGGTAATATTTA | 55666 |
rs200823885 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613140 | AAAAAAAAAAAAAAA[A/C]AAAAACTGATAAAAA | 55666 |
rs200839096 | in-del | -/T | 0.0505692 | 0.150756 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595956 | TATGCTGTTAAGTTG[-/T]TCAGAATTTTTACCA | 55666 |
rs200845145 | snp | C/T | 0.000548177 | 0.0165465 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606703 | CACCTGTCTGTTCAG[C/T]GTGATGGCGCTCGGC | 55666 |
rs200887018 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626315 | AGCGAGACTCCATCT[A/C]AAGAAAAAAAAAAAA | 55666 |
rs200891361 | snp | A/G | 4.01873e-05 | 0.00448241 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613491 | GAACAACAAATCGCC[A/G]TGCCTGTTCAAATGA | 55666 |
rs200894370 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604128 | TTGGTGGCAGTTTTT[A/C]TTACTCTGGTGACAC | 55666 |
rs200897859 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631437 | TATATATATATATAT[-/A]TTTTTTTTTTTTTTT | 55666 |
rs201018577 | in-del | -/AC/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623808 | TCTCAAAAAAAAAAA[-/AC/C]CAAAACTCAATTCCA | 55666 |
rs201095089 | snp | A/G | 0.00419107 | 0.0455847 | synonymous-codon, nc-transcript-variant, missense | NPLOC4 | GRCh38.p7 | 17:81559406 | ACCTGGGAGCTGCCC[A/G]CCAACTGTGCCTGCA | 55666 |
rs201125620 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606022 | AGATGGGGTTTCACC[A/G]TATTGGCCAGGCTGG | 55666 |
rs201148025 | in-del | -/CT | 0.0337553 | 0.125452 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595479 | TGAGATGGAGTTTCA[-/CT]CTGTCGCCCAGGGGA | 55666 |
rs201157898 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610976 | AAAAAAAAAAAAAAA[A/T]AAAAATGACACAAAC | 55666 |
rs201193802 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595538 | TATATATATATATTT[A/T]TTTTTTCTTTTCTTT | 55666 |
rs201196525 | in-del | -/CC | 0.0260105 | 0.111035 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593942 | AAATTCCCAACCCTT[-/CC]CCCTTAAGCACTCAA | 55666 |
rs201247928 | snp | C/G | 9.5915e-05 | 0.00692447 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589136 | TTTAAAAAGAGTCTA[C/G]CAAACGGCATTCAAA | 55666 |
rs201253145 | in-del | -/A | 0.0185938 | 0.0946107 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560700 | AACAAACAAACAAAC[-/A]AACAACAACAAAAAA | 55666 |
rs201348535 | in-del | -/TTCT | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567222 | TGAAAAAATTAATCT[-/TTCT]ATCAACAAGCTTCTT | 55666 |
rs201438094 | in-del | -/CAAA | 0.0232847 | 0.105357 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574862 | CTACAAGACTGTCTC[-/CAAA]CAAACAAACAAACAC | 55666 |
rs201447365 | snp | C/T | 9.85115e-05 | 0.00701755 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589141 | AAAGAGTCTACCAAA[C/T]GGCATTCAAAACCAG | 55666 |
rs201452920 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605294 | TCAAAAAAAAAAAAT[A/T]AATAATAATAATAAT | 55666 |
rs201470806 | snp | A/G | 4.99089e-05 | 0.00499519 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622295 | TAAAACAAGGCCCAA[A/G]GAACAGAAATTTAAT | 55666 |
rs201486683 | in-del | -/ATA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595532 | TATACATATATATAT[-/ATA]TTTTTTTTTTCTTTT | 55666 |
rs201591319 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595532 | ATACATATATATATA[-/T]TATTTTTTTTTTCTT | 55666 |
rs201622340 | snp | A/C/G | 0.00526444 | 0.0510379 | missense, nc-transcript-variant, synonymous-codon | NPLOC4 | GRCh38.p7 | 17:81559396 | ACTCATGGAGACCTG[A/C/G]GAGCTGCCCGCCAAC | 55666 |
rs201672516 | snp | A/G | 0.000755365 | 0.0194194 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81610249 | TTTCCCCAAAGGGCC[A/G]TGGCGGCATCTGAGG | 55666 |
rs201672898 | in-del | -/AAAC | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560681 | TAAGCCGAGATCTCA[-/AAAC]AAACAAACAAACAAA | 55666 |
rs201676312 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619552 | GAAACTCTGTCTCAA[-/G]GAAAAAAAAAAAAAA | 55666 |
rs201724783 | snp | C/T | 0.000229312 | 0.0107053 | synonymous-codon, nc-transcript-variant, missense | NPLOC4 | GRCh38.p7 | 17:81559316 | TGGCTGGTTCATGAA[C/T]GTGCAGTGCTGACAG | 55666 |
rs201727641 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592530 | AAACCTTTCAGTAAA[-/T]ACCAATTCCAGAGGT | 55666 |
rs201734942 | in-del | -/TTG | 0.100231 | 0.200173 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638299 | AGAGTTTTTTGTTTT[-/TTG]TTTTTTTTTGTTTTT | 55666 |
rs201788859 | snp | C/G | 0.0185559 | 0.094518 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589131 | AGACCTTTAAAAAGA[C/G]TCTACCAAACGGCAT | 55666 |
rs201813049 | in-del | -/A | 0.217551 | 0.247885 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605294 | TCAAAAAAAAAAAAT[-/A]AATAATAATAATAAT | 55666 |
rs201850065 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633140 | CTCAAAAAAAAAAAA[A/G]AAAAGAAAAGAAATA | 55666 |
rs201851704 | in-del | -/AAG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621111 | AAAGAAAGAAAAGGA[-/AAG]AAGGAAGGAAGGAAA | 55666 |
rs201917572 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606024 | ATGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 55666 |
rs201933742 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618532 | CCCGTCCGGGAGGGA[C/G]GTGAGGGGTCAGCCC | 55666 |
rs201948322 | snp | C/T | 8.29167e-05 | 0.00643828 | missense, upstream-variant-2KB, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613411 | GGAGCGCCAAAGACT[C/T]TGAAGCCCGGTGGAA | 55666 |
rs201962296 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626317 | CGAGACTCCATCTCA[A/G]GAAAAAAAAAAAAGA | 55666 |
rs202010871 | snp | A/T | 1.65641e-05 | 0.00287781 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622237 | GTTTCTATTGATGTA[A/T]ACCGAGAAGCCATTA | 55666 |
rs202028445 | in-del | -/AAAAAAAAAAG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628214 | AGACTCCCTCTCATA[-/AAAAAAAAAAG]AAAAAAAAAAGAAAA | 55666 |
rs202045831 | snp | A/G | 0.00147396 | 0.0271073 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597222 | GCCATAGGGCCACAC[A/G]CACAGTCCTGTCTCC | 55666 |
rs202081141 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563588 | AAGGGAAACAAAAAA[A/G]AAAAAAAAAAAAAAG | 55666 |
rs202133528 | snp | A/G | 0.000194903 | 0.00986984 | synonymous-codon, nc-transcript-variant, missense | NPLOC4 | GRCh38.p7 | 17:81559415 | CTGCCCGCCAACTGT[A/G]CCTGCAGGGTGGAAG | 55666 |
rs202138659 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630290 | TTTTCTAATTGTTAC[-/T]TTTTTTTTTGCTTTT | 55666 |
rs202144955 | in-del | -/A | 0.0115144 | 0.0749975 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615835 | TATCCAGTACACAGC[-/A]AAAAAAAACCAACAA | 55666 |
rs202164291 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599858 | CAGGAAATTAAATGA[C/T]GATTGATGACGGAGC | 55666 |
rs202194535 | in-del | -/ACCATTACC | 0.0236746 | 0.106192 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596642 | TATCTACAATTCCTA[-/ACCATTACC]AATTCCTCATCTAAA | 55666 |
rs202225283 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595810 | GGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 55666 |
rs202238198 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581375 | AAAAAAAAAAAAAAA[A/C]AGTTAATAAAATCAC | 55666 |
rs367545000 | snp | A/G | 4.97905e-05 | 0.00498926 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596252 | GGTGTCCTAAGACAA[A/G]AGAAGCAGCCTATCA | 55666 |
rs367554743 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592227 | GGATGTGGGACGGGA[A/G]TGCAACAAGTACAAT | 55666 |
rs367594910 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601998 | GGTGATCTCCACAAG[A/T]CAGTGTTAGGTGGAA | 55666 |
rs367613880 | snp | A/C/T | 0.000101327 | 0.00711712 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613268 | ATTTCCCTTTATTCA[A/C/T]CCATTAAGATCACCA | 55666 |
rs367697592 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559836 | CTCCCGGGTTCAAGC[A/G]GTTTTCCTGCCTCAG | 55666 |
rs367793663 | snp | C/T | 0.212728 | 0.247206 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563164 | CACTACAACCTACGC[C/T]TCCTGGGTCAAGTGA | 55666 |
rs367804097 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557238 | CCAGGGCCTGAACTC[C/T]CACAGCAGGGCTCAC | 55666 |
rs367838449 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596365 | TAATTCCAGCACTTT[-/T]GAGAGGTGGAGGCGG | 55666 |
rs367845988 | in-del | -/GGAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621124 | GAAAGAAGGAAGGAA[-/GGAA]AGAAAAGAAAAAAAA | 55666 |
rs367858990 | snp | A/G | 2.09159e-05 | 0.00323381 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572110 | TAGTCAGAGGGGAAC[A/G]GCGGTGAGCAAAGAC | 55666 |
rs367931915 | snp | C/T | 0.000530583 | 0.0162791 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597196 | TGCAGGCCAACACCA[C/T]CTGTAACCAAGCCAT | 55666 |
rs367957170 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605852 | TTTGAGACGGAGTCT[C/T]GCTCTGTCACCCAGG | 55666 |
rs367969907 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629147 | CCTCCCAAAGTGCTG[A/C]GATTACAGGCGTCAG | 55666 |
rs367972858 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621010 | CCTGGGTGACACGGT[A/G]AGATTCTGTCTCAAG | 55666 |
rs367982123 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620738 | GAGGGCAAGAGCAGC[A/G]GGACAAGCGTGGTCG | 55666 |
rs367982791 | in-del | -/AA | 0.216649 | 0.247765 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611960 | GCGAGAGTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 55666 |
rs367985830 | snp | C/T | 0.000165631 | 0.00909881 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613378 | AGGTACTGATCAATC[C/T]CATCCTCCACCACGT | 55666 |
rs368004865 | snp | A/G | 0.00109424 | 0.023365 | synonymous-codon, nc-transcript-variant, missense | NPLOC4 | GRCh38.p7 | 17:81559370 | GTGTGTGGAGCCCCC[A/G]ACGGCGCCGTACTCA | 55666 |
rs368006340 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631526 | CAAAGGGCATTACTT[C/T]CTAAGACAACTTGAT | 55666 |
rs368009274 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575140 | AGTCTCGCTCTGTCG[C/T]CCAGGCTGGAGTGCA | 55666 |
rs368019890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600627 | TGCTGCACCTTTTAC[A/C]AGGGCTGCAAAACAT | 55666 |
rs368085521 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594310 | AAAAAAAAAACTGAC[A/T]CAACTAATTCACTTG | 55666 |
rs368125171 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577682 | CCATCTTCAAACTCT[A/G]CGTGCTGGCACCTGG | 55666 |
rs368163496 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582021 | CCCTAGTGTCAGAGA[A/G]GGAACATGAGGAGGG | 55666 |
rs368177782 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588204 | TGAAATGAAATGAAC[A/G]GAGTATCAGTAAACT | 55666 |
rs368213434 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595794 | AGCGATCCACTCACC[C/T]GGGCCTCCCAAAGTG | 55666 |
rs368216072 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621051 | AAAGGAAAAGGAAAA[G/T]AAAGGAAGGAAGGAA | 55666 |
rs368218835 | snp | A/G | 4.9812e-05 | 0.00499034 | synonymous-codon, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81588992 | GCTAGACTCCTTGGC[A/G]TAGCCAAGCTCCGGG | 55666 |
rs368226050 | snp | C/T | 0.000124406 | 0.0078859 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604685 | GAAAGCGGTCAGCGA[C/T]GGTGTGATTCTCAAA | 55666 |
rs368298389 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616278 | GTGAGCTGAGATCGC[A/G]CCACTGCACTCCAGC | 55666 |
rs368307791 | snp | C/G | 3.31345e-05 | 0.00407016 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597239 | ACAGTCCTGTCTCCA[C/G]CTCACCTTATTTCGA | 55666 |
rs368372520 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593952 | ACCCTTCCCTTAAGC[A/G]CTCAACCCAAGCAAC | 55666 |
rs368473509 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617016 | GCATGCCAGGTCCCA[C/T]CGATGCATCTACAGC | 55666 |
rs368492583 | snp | A/G | 0.000177546 | 0.00942026 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559424 | AACTGTGCCTGCAGG[A/G]TGGAAGAGAAATGAG | 55666 |
rs368505831 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570690 | AACCCCAGTAACACT[A/G]GCTGGTGCCTTTTCC | 55666 |
rs368551905 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585790 | CTAGGAGTTCAAGAC[C/T]AGCCTGGGCAACATG | 55666 |
rs368555670 | snp | C/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560617 | AAGGCTGAGGAAGGA[C/G]AATGGCGTGAACCTG | 55666 |
rs368564494 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623024 | ACATGGTGAATCCCC[A/G]TTTCTACTAAAACTA | 55666 |
rs368593164 | snp | C/T | 0.00018539 | 0.00962603 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606643 | TCTTCTGGAAATATC[C/T]GTTTCTCAGCCATGA | 55666 |
rs368650374 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593127 | TAGGCAAAAACCACT[A/G]CTTACAATGATATGA | 55666 |
rs368656583 | snp | A/G | 0.000138284 | 0.00831401 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81610231 | AGGGACGCAGTGCAC[A/G]CATTTCCCCAAAGGG | 55666 |
rs368658448 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606267 | CAGGCTACTCAGAGG[C/T]GGGACAAGGACAGCA | 55666 |
rs368707657 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635507 | AGAACAGCCTTGCAA[A/G]TAAGTGCTAGGTTCT | 55666 |
rs368793482 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581737 | TCAGATTCCAGACAC[C/T]AGAGCCACTGTCCCA | 55666 |
rs368815487 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571377 | GGTACAGCCATGTCT[A/C]CATGACCATAAAATG | 55666 |
rs368830964 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578871 | CTTACCAATCTACAA[C/T]ATTTAATTTTTTCAT | 55666 |
rs368860031 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606234 | CTCTAAGGGCACAGC[A/G]GCAGGAGGAAGGCGA | 55666 |
rs368887806 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580259 | GCACTAGCACATCGC[C/T]GACAGATCCCCAGCC | 55666 |
rs368950526 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612038 | AAAGGGCCTGAGAGC[A/G]GTGCATAAATAATCC | 55666 |
rs368996464 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617784 | CTGCCTCAGCCTGCC[A/G]AGTGCCTGCGATTGC | 55666 |
rs369031850 | snp | C/G | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81597272 | GTAGCGGACGGTACC[C/G]TTTCGGGTATCTTCT | 55666 |
rs369171742 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607514 | GTCCACACTGTGGAA[C/T]GGCTAAATTGAGCTA | 55666 |
rs369221002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561865 | GGCCTCCTAGAGTGT[C/T]AGGATTATAGCTATG | 55666 |
rs369247089 | snp | C/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563548 | GCACTCCAGCCTAGG[C/T]AACAGAGTGAAACCC | 55666 |
rs369275603 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593927 | CCTTCAATCCTAGCC[C/T]AAATTCCCAACCCTT | 55666 |
rs369348679 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558316 | CCAGAGCATCGGCAC[C/T]GGTGACCCAGCTCTC | 55666 |
rs369358806 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618428 | CCGCCCCGCAGCCGC[C/T]CCGTCTGGGAAGTGA | 55666 |
rs369490885 | snp | A/C/G | 0.000126732 | 0.00795942 | synonymous-codon, missense, nc-transcript-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81559289 | GCTGCACATCTCGCA[A/C/G]TGGCCTGTGCCTGGC | 55666 |
rs369495645 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581583 | GAGGGGCAGCCAGTC[C/G]TCCACAGCACCAAGG | 55666 |
rs369497535 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633751 | CTCTGTCACCCAGAG[C/T]GGGAGTGCGATGGCG | 55666 |
rs369540799 | snp | C/T | 0.000209256 | 0.0102266 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600313 | AGCCTGGCCACGCCC[C/T]CTGCTTGGCTGCCGG | 55666 |
rs369622280 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630528 | TCAAGTGATCCTGCC[A/G]CTGTGCTGGGATTAC | 55666 |
rs369631635 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559950 | ATGTTGGCCAGGCTG[A/G]TCTCGAACTCCTGAC | 55666 |
rs369659340 | snp | A/G | 0.000117107 | 0.00765112 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606754 | ATTCGGCCACGGGAG[A/G]TGCCCCTCGCACCCT | 55666 |
rs369663479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568196 | TGGGGCCCCCTTCAC[A/G]GCAGGGAGACAGGTC | 55666 |
rs369678889 | snp | C/G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620973 | GGCTGCAGTGAGCTA[C/G/T]GATCGCACCACCGCA | 55666 |
rs369692023 | in-del | -/GAAC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594951 | TGTCTCAAAACAAAC[-/GAAC]AAACAAAAAAAAAAA | 55666 |
rs369699111 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634740 | ACAGGTGCATGCCAC[A/C]ACACCCGGCTAATTT | 55666 |
rs369798780 | snp | C/T | 0.000161987 | 0.00899817 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613464 | GGGCCCAGCAAGGCT[C/T]GAGGGAAACAGGAAC | 55666 |
rs369821874 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616300 | CACTCCAGCCTGGGC[A/G]ACATAGCAAGACTCT | 55666 |
rs369822561 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618100 | TGGGAAGTGAGGAGC[C/G]TCTCTGCCTGGCCGC | 55666 |
rs369826429 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602430 | AAAAATCAGGCCGGG[C/T]GCAGTGGCTCACGCC | 55666 |
rs369877767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597952 | AGAAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGT | 55666 |
rs369916559 | snp | A/T | 1.65883e-05 | 0.00287991 | synonymous-codon, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81589046 | CTCATCACGGACCAG[A/T]GCCATACACTGATTG | 55666 |
rs369976141 | snp | A/C | 0.125874 | 0.217008 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624611 | TCAAAAAAAGAAAAA[A/C]AAAAAAAAGACAAGG | 55666 |
rs370035498 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580603 | TCTCCTCCAGACACC[C/G]CCAGAGCTGCTCTGC | 55666 |
rs370050181 | snp | G/T | 1.65679e-05 | 0.00287814 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622156 | TGCTTCCTCCTCAGA[G/T]GACACTTACTTGATT | 55666 |
rs370124399 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578125 | AGCTTCCCGCCTCCA[A/G]ACCACCCCTCCTGAC | 55666 |
rs370141362 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621003 | ACTCCAGCCTGGGTG[A/C]CACGGTGAGATTCTG | 55666 |
rs370143967 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619480 | TTGAACCCGGGGGGG[-/G]CAGAGGTTGTGGTGA | 55666 |
rs370267564 | snp | C/G | 1.66277e-05 | 0.00288333 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596277 | CTATCAAATTTTACA[C/G]CATCATGCCAAAATA | 55666 |
rs370288783 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627430 | GTGGGGAACAAAAAT[C/G]AACTGTCAACTCAGA | 55666 |
rs370380865 | snp | C/T | 0.000948935 | 0.0217616 | synonymous-codon, intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81608736 | TGCTTACTTGTCAGC[C/T]CCTCCAGTCAGCTTC | 55666 |
rs370394546 | snp | A/G | | | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565010 | CACGAGTGGGGAATC[A/G]TTCAGGACCTGGTGA | 55666 |
rs370403982 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604491 | GCCTCTCCGAAAGGG[C/T]GTCCCCCACAGCCTC | 55666 |
rs370407971 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629643 | GGAAAATAAGAAAAC[A/G]AGGAAAAGAGAAAAG | 55666 |
rs370443079 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587516 | GAGACGGGGTTTCAC[A/C]GTGTTAGCCAGGATG | 55666 |
rs370456211 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581489 | CAACCAATTCTCCCT[A/G]CCCCAGAGGAATAAG | 55666 |
rs370461248 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594631 | ATACAAAAAATTAGC[C/T]GGGTATGCTGGCAGG | 55666 |
rs370487624 | snp | C/G | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638636 | AATTTGGTGGGTATG[C/G]GGTCAGAAAGTAGGG | 55666 |
rs370500361 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626103 | GCAGTGGGCAGAGAT[C/T]GCGCCACTGCACTCC | 55666 |
rs370510838 | snp | A/C/G | 0.000134881 | 0.0082112 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604593 | AGCCCTGATGCCAAG[A/C/G]GGAATGTCTTTGTGC | 55666 |
rs370512436 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559028 | GAGGAGCCGCTCTGC[A/G]TTTCCAGTCTGGAGA | 55666 |
rs370545742 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620114 | GGAAGAGATGGAAGG[C/G]GAACCTGAAGATTAC | 55666 |
rs370550311 | snp | A/G | 0.000115945 | 0.00761308 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596156 | GGATCCAAAATGTCC[A/G]TCTGGAGAGAGCCGG | 55666 |
rs370648770 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617254 | AGACAGATTTAGGGG[-/G]AAAAAAAATCAGATT | 55666 |
rs370660725 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605146 | CAGAGCCAGGCGTGG[C/T]GGCGGGCGCCTGTAG | 55666 |
rs370706702 | in-del | -/AC | | | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81564084 | AGGCTCCAGCTCAAA[-/AC]ACACACACACACACA | 55666 |
rs370718857 | snp | C/T | 3.31724e-05 | 0.00407248 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81569048 | CATCCCGGTTTTCAA[C/T]AGGAAATGGATTTTG | 55666 |
rs370817432 | snp | A/T | 0.00019841 | 0.00995819 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571993 | TGGGTCCACCTGCCC[A/T]AGCTGTGCATGGGGG | 55666 |
rs370854547 | snp | A/G | 0.000468368 | 0.0152959 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608842 | CAAGACACAGAGTAA[A/G]CGAGTGCAGTCTCAC | 55666 |
rs370935364 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577654 | CTGAGTCCTGGCAAC[C/T]GTCTGTCCTGCTCCA | 55666 |
rs370948703 | snp | C/T | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635444 | CCAGGTTGGGAAACA[C/T]GGAGGCACCAAGAGG | 55666 |
rs370977120 | snp | C/T | 0.000159987 | 0.00894249 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81610237 | GCAGTGCACGCATTT[C/T]CCCAAAGGGCCGTGG | 55666 |
rs370996433 | snp | A/G | 1.65638e-05 | 0.00287778 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596175 | GGAGAGAGCCGGCAC[A/G]TGTTGGGATGCTTGT | 55666 |
rs371034483 | snp | C/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638529 | TCTTGAACTCCTGAC[C/T]TCAGGTGATCCGCCC | 55666 |
rs371049924 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573966 | CAGGATGGGCTTCCG[C/T]ATTCTGCGCTCTGCT | 55666 |
rs371069890 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589357 | AACACGGTGAAACCC[C/T]GTCCCTACTAAAAAT | 55666 |
rs371082995 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614896 | ACAAGACACACACAC[-/AG]GGGACAGTCTGAGAG | 55666 |
rs371097753 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591390 | CGATGAGCTGAGATC[A/T]TACCACTGCACTCCA | 55666 |
rs371100522 | snp | C/G | 1.9158e-05 | 0.00309494 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81572053 | AGGCAGGGGCCGGGC[C/G]AGCTGGGTGATCTCG | 55666 |
rs371129149 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633771 | GTGCGATGGCGCGAC[C/G]TCGGTTCACTGCAAC | 55666 |
rs371131416 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633861 | TAGGCGCCCGCCACC[A/G]CGCCCAGCTAATTTT | 55666 |
rs371136316 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619505 | TGGTGAGCTGAGACC[A/T]TGCCACTGCACTCTA | 55666 |
rs371146892 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620980 | GTGAGCTACGATCGC[A/G]CCACCGCACTCCAGC | 55666 |
rs371218909 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587865 | TTTTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 55666 |
rs371263349 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570304 | GATCGGAGTACTCGC[C/T]TCCTGGGTGCCCAGC | 55666 |
rs371284424 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622371 | CTAGAAGAGTATTCA[A/C]CAAATTTGGAAAGTG | 55666 |
rs371318415 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599396 | AATTAGGTCAAAAAA[C/T]TGGACCAATCTCTTT | 55666 |
rs371355414 | snp | C/T | 1.65622e-05 | 0.00287764 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81597275 | GCGGACGGTACCCTT[C/T]CGGGTATCTTCTGAG | 55666 |
rs371360326 | snp | A/C/T | 9.94191e-05 | 0.00704987 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613349 | TTCTGTAAATCTTCC[A/C/T]GTCCTGTTTGCTGAG | 55666 |
rs371370139 | snp | C/T | 8.91703e-05 | 0.00667661 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81565576 | TCCTCATTTCTGGTC[C/T]GCACGGCCTCCAGCA | 55666 |
rs371406645 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589398 | GCTGGGTGCGGTGGC[A/G]GGCGCCTGTAGTCCC | 55666 |
rs371448578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634072 | ACGTGGGGTTTCACC[A/G]TGTTGCCCAGGCTGG | 55666 |
rs371459339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606065 | GACCTCAGGTGATCC[A/G]CCCACCTCAACCTCC | 55666 |
rs371471192 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575232 | AGCCTCCCGAGTAGC[C/T]GGGACTACAGGTGCC | 55666 |
rs371479866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610681 | AACCAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 55666 |
rs371479948 | snp | A/G | 0.000132809 | 0.0081478 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606712 | GTTCAGCGTGATGGC[A/G]CTCGGCTGGCACTTA | 55666 |
rs371481275 | in-del | C/TA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612734 | AAAATCTAAAATAAA[C/TA]AATGTACATATGCAT | 55666 |
rs371486676 | snp | A/G | 0.00129157 | 0.0253795 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559256 | CAGCAGAGGGCAGGC[A/G]CCCTAGGTCCTGGGG | 55666 |
rs371526150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615203 | CTCACGGGTTTAAGC[A/G]ATTCTCCTGCCTCAG | 55666 |
rs371547793 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631042 | GCTGGGCGTGGTGGC[A/G]GGCACCTGTAATCCC | 55666 |
rs371591214 | snp | A/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638086 | TACATTAATTGATTA[A/T]ATTATGTTAGTAATT | 55666 |
rs371624424 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631558 | TTTATGCTGATGAAA[A/G]CCATCGTGAAGGTGA | 55666 |
rs371680934 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567950 | CAGGCTTGGTGGCGC[A/G]CACCTATAATCCCAG | 55666 |
rs371697933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586272 | GACACAGGAATTTCA[A/G]ACATGCAGCCATTCT | 55666 |
rs371762798 | in-del | -/AT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605294 | CAAAAAAAAAAAATA[-/AT]AATAATAATAATAAT | 55666 |
rs371767641 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570936 | ACTTAACTTCCTTTA[A/T]AAAAGAAGAGGAAAG | 55666 |
rs371835980 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620648 | CACTGTTTTCTGAGG[C/T]GTTCAGTACGTATTT | 55666 |
rs371846884 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593472 | ATCACTTTCCCCTGA[C/T]GTTACAGTTAGGATA | 55666 |
rs371874629 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577080 | GCCAACAAACCCCAC[A/G]GCCTGCTGAGTAAGC | 55666 |
rs371880422 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566903 | TTCTGCAAAGCACTC[A/G]CCCTCTTCTCCCCCA | 55666 |
rs371889199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630397 | GGTTCAAGTGATCCT[C/G]TGACCTCAGCCTCCC | 55666 |
rs371890445 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616310 | TGGGCGACATAGCAA[A/G]ACTCTGTCTCAAAAA | 55666 |
rs371916652 | snp | C/T | 1.66263e-05 | 0.00288321 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597361 | TCTCCTCAAGATAGA[C/T]GATGAATGGCTGGGC | 55666 |
rs371929940 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626670 | AAACCCCATCTCTAC[C/T]AAAAAATTAAGAAAT | 55666 |
rs371943006 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617262 | TTAGGGGGAAAAAAA[A/T]TCAGATTACGTATTT | 55666 |
rs371964574 | snp | A/G | 6.45599e-05 | 0.00568118 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572118 | GGGGAACAGCGGTGA[A/G]CAAAGACGATCAGTA | 55666 |
rs371987138 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81556973 | TGCACACCTGTGAGC[C/T]GAAACAGAGCCGAAG | 55666 |
rs372009025 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633216 | AATACCCCAGAAAAA[C/T]GTTTTCACAATATAT | 55666 |
rs372065924 | in-del | -/A/AAAA | 0.0217236 | 0.101931 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585170 | CGAGACTCTGTCGCC[-/A/AAAA]AAAAAAAAAAAAAAA | 55666 |
rs372078430 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606488 | AGAGAACTGAGGGCG[C/T]GCACTCCATATCTCC | 55666 |
rs372108702 | snp | C/G | 5.26191e-05 | 0.00512901 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559432 | CTGCAGGGTGGAAGA[C/G]AAATGAGCACTCATC | 55666 |
rs372128669 | snp | C/T | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556616 | CAGGGCTGACAGGTG[C/T]GGCAGAGGCAGAAGA | 55666 |
rs372137359 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621070 | GGAAGGAAGGAAGGA[-/A]GTATCAAGATGCAAA | 55666 |
rs372146648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564541 | ACACCTGTAATCCCA[A/G]CACTCTGGGAGGCAG | 55666 |
rs372168431 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595363 | CGCTTGAACCCAGGA[A/G]GCGGACGTTGCAGTG | 55666 |
rs372202202 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617181 | GCCAATGTGGCAGCA[C/G]AGCAGAAACTAGGAG | 55666 |
rs372219665 | snp | C/T | 0.000165739 | 0.00910175 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597221 | AGCCATAGGGCCACA[C/T]GCACAGTCCTGTCTC | 55666 |
rs372297062 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619962 | GCCTCTGTTTACCGC[G/T]TTGCATCGGCAGGAA | 55666 |
rs372316669 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623919 | ATTCACTCATTCCTT[C/G]AACAAATATTAAGCA | 55666 |
rs372350386 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616281 | AGCTGAGATCGCACC[A/G]CTGCACTCCAGCCTG | 55666 |
rs372434085 | snp | A/G | 3.31763e-05 | 0.00407272 | synonymous-codon, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81589010 | GCCAAGCTCCGGGGC[A/G]TCCTTGCATGGCAGC | 55666 |
rs372482870 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621014 | GGTGACACGGTGAGA[C/T]TCTGTCTCAAGAAAA | 55666 |
rs372483015 | snp | A/G | 0.213333 | 0.247296 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563178 | CTTCCTGGGTCAAGT[A/G]ATTCTCCTGCCTCAG | 55666 |
rs372486393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579250 | GGGCGTGGTGGTGGG[C/T]GCCTGTAATCCCAAG | 55666 |
rs372534606 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624982 | GAATCATCATCCACA[A/G]AATCCCTGTTGCTCA | 55666 |
rs372575370 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623832 | AATTCCAATTCTGAA[A/T]CCTAACACAGAATGG | 55666 |
rs372604012 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571053 | TGTTTTCATCTTAAT[C/T]ACACCCTAGGTAGTC | 55666 |
rs372612146 | snp | C/T | 0.000839513 | 0.0204708 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565459 | AGAGTGGGCTGCTCT[C/T]CGGCCCCAGCCACGG | 55666 |
rs372695343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589754 | TGTAATCTGAGCACT[C/G]TGAGAGGGCAGGGCG | 55666 |
rs372731175 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573300 | AAGCAAATCTCCCTG[A/G]GGTGTGCAGGGTGAC | 55666 |
rs372818795 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577965 | ATGGGTCTTCTACAG[C/T]GGGGACCTCCCCTGC | 55666 |
rs372834422 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610678 | ACAAACCAGGCCGGG[C/T]GCGGTGGCTCACGCC | 55666 |
rs372876711 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620969 | TCGAGGCTGCAGTGA[A/G]CTACGATCGCACCAC | 55666 |
rs372900375 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569164 | TGAAAATGGTGTGGC[C/G/T]GACTCCCAGCCAGCC | 55666 |
rs372948602 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578437 | CTAACACCTGACCCA[C/T]GGGAAGCTCTCAACA | 55666 |
rs373000332 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596433 | GCCAACACACCAAAA[C/T]CTGGTCTCTACTAAA | 55666 |
rs373049843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582979 | CAGGCCTCCTCCCTG[C/T]GGCGCCGCCCCTGCG | 55666 |
rs373061371 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598689 | CCGCCTCTGCCTGTG[A/T]ATTCCTGCACCAGAA | 55666 |
rs373063460 | snp | A/C/T | 4.96918e-05 | 0.00498436 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596169 | CCGTCTGGAGAGAGC[A/C/T]GGCACATGTTGGGAT | 55666 |
rs373068966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620974 | GCTGCAGTGAGCTAC[A/G]ATCGCACCACCGCAC | 55666 |
rs373091840 | snp | C/T | 1.97924e-05 | 0.00314576 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606820 | AAACTTCCCCCTACA[C/T]AGAAGAGAAGCAACT | 55666 |
rs373093498 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603942 | ACACACACAGCCCAA[C/T]TCCCAAAAACCAGAA | 55666 |
rs373120873 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590045 | AAGCGGGTGGGAGAA[G/T]AGCAAGACGGAAACT | 55666 |
rs373130883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616489 | TAATCCCAGCACGTT[C/G]GGAGGCCGAGGCAGG | 55666 |
rs373144973 | snp | G/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562744 | AAGAGTTCAAGACCA[G/T]CCTGGGCAACATAGT | 55666 |
rs373146485 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576109 | AAGACATGAGGAGAC[A/G]CAGATACCTTGTTTT | 55666 |
rs373165450 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618121 | GCCTGGCCGCCCATC[A/G]TCTGGGATGTGACGA | 55666 |
rs373213933 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627188 | GAGGTCAGGAGATCG[A/C]GACCATCCTCACTAA | 55666 |
rs373223988 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558011 | GGGCCAGCCTCTCCC[A/G]TGGGTGCAGAGCAGC | 55666 |
rs373245945 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602557 | AAATTACAAAAATTA[A/G]CCAGGCGTGGTGGCG | 55666 |
rs373277639 | snp | C/T | 0.000579734 | 0.0170156 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596138 | CACTGCAGTAACAAA[C/T]TTGGATCCAAAATGT | 55666 |
rs373335865 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629959 | AGCTCAATCCTTCTA[C/G]AATATGATGCCGAGG | 55666 |
rs373374615 | snp | A/G | 8.28411e-05 | 0.00643535 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629828 | AAACAAAACATGATG[A/G]TTACTGCACAGCCTA | 55666 |
rs373408523 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590744 | TCAGAAAACAGAAAC[A/G]TAGTGCACATGGCTG | 55666 |
rs373454484 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559728 | GGGTTGTTTCCAGCT[-/T]TTTTTTTTTTTTTTT | 55666 |
rs373549438 | in-del | -/ACAC | 0.135005 | 0.221982 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574877 | CAAACAAACAAACAA[-/ACAC]ACACACACACACACA | 55666 |
rs373589502 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563827 | ATGGATGCAGTTGAA[A/G]GCCATTATTCTAAGC | 55666 |
rs373600266 | snp | C/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638030 | ATACATATTTCACAA[C/T]ATCACAATTACTGTG | 55666 |
rs373619762 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634205 | GACGTGGTTTCACCA[C/T]GTCGGCCAGGCTGGT | 55666 |
rs373625308 | snp | A/G | | | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565036 | GGTGACTGAGGGTCC[A/G]GAAGACACGCAATGC | 55666 |
rs373626859 | snp | A/T | 1.72701e-05 | 0.0029385 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604563 | CTGAGGTGGCTCATA[A/T]ATCGCAGCCACTTCA | 55666 |
rs373652080 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626044 | ATCCCAGCTACTCAG[G/T]AGGCTGAAACAGGAG | 55666 |
rs373658625 | snp | A/C | 0.212728 | 0.247206 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563160 | AGCTCACTACAACCT[A/C]CGCTTCCTGGGTCAA | 55666 |
rs373669439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627632 | TAATCCCAGCTACTC[A/G]GAAGGCTGAGGCAGA | 55666 |
rs373674387 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605731 | GAGGATGGAGATGGG[C/T]TTCATCTATCAATAA | 55666 |
rs373700096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628198 | CCTTGGAGACAGAGC[A/G]AGACTCCCTCTCATA | 55666 |
rs373711703 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566161 | ACGTGGCGAAACCCC[A/G]TCTCTACTAAAAATA | 55666 |
rs373722008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593144 | TTACAATGATATGAG[A/G]TTAGAAGCAATTCTG | 55666 |
rs373766819 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571744 | GGTCCTTTGTACTTT[A/G]GTATGGGGACAGTTA | 55666 |
rs373767656 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574740 | GGGGATGCCCAGGGC[A/C]CAGTGGCTCATGCCT | 55666 |
rs373774578 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561492 | CCTATTTTTATGCCA[A/G]TGTTTTTCTGTGTTC | 55666 |
rs373784304 | snp | C/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562517 | GCACTCCAGCCTGGG[C/G]AACAGAACAAGACTT | 55666 |
rs373789389 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577716 | CACCATCCTCCCACA[A/C/G]AGACCCATGGCTCTA | 55666 |
rs373789943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591598 | GCTGTTTATAAACAG[C/T]AAAATTGGCCATATG | 55666 |
rs373904233 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594737 | CCGAGATCGCGCCAC[C/T]GCACTCCAACCTGGG | 55666 |
rs373904474 | snp | A/C/G | 6.24649e-05 | 0.00558825 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81559292 | GCACATCTCGCAGTG[A/C/G]CCTGTGCCTGGCTGG | 55666 |
rs374025768 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631908 | AGTTCAAGTGATTCT[-/T]CCTGCCTCAGCCTCC | 55666 |
rs374060768 | in-del | -/CTTT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590704 | CCTCTATTTCAGTTT[-/CTTT]GACAAAAAGAATCAC | 55666 |
rs374070908 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633930 | GGAGTGCAGTGGTGC[A/G]ATCTCGGCTCACTGC | 55666 |
rs374093126 | snp | G/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638667 | AGTGTTGATTGGTTG[G/T]GTCAGAGGTGAAATG | 55666 |
rs374097896 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626723 | GGATCGTTTGAGCCC[A/G]GGAAGTCAAGGCTGC | 55666 |
rs374116076 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560184 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 55666 |
rs374213379 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591728 | CCGGAATGGCTGGCA[A/G]GACAAGTTAACTATC | 55666 |
rs374217101 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571076 | AGGTAGTCTAAAAAC[A/C]AGATGCCTTCACGGC | 55666 |
rs374224599 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621015 | GTGACACGGTGAGAT[C/T]CTGTCTCAAGAAAAG | 55666 |
rs374243889 | in-del | -/TCTATAATCCCAGCA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585726 | TCTGTAATCCCAGCA[-/TCTATAATCCCAGCA]CTGTGGGAGGCTGAG | 55666 |
rs374269815 | snp | C/T | 0.000138619 | 0.00832409 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81610230 | GAGGGACGCAGTGCA[C/T]GCATTTCCCCAAAGG | 55666 |
rs374288121 | snp | A/G | 1.95295e-05 | 0.0031248 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567422 | GGACACGCACCTGCA[A/G]AGGCATAACTTCATT | 55666 |
rs374293898 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81639053 | AGTTATTTCAGCCTA[C/T]ACCCAGGAATGAACA | 55666 |
rs374327554 | snp | A/G | 0.000161987 | 0.00899817 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81572071 | CTGGGTGATCTCGTT[A/G]CCAAACTTGTCTACG | 55666 |
rs374369333 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579013 | GCAGCCTCGAACTCC[C/T]GGGCTCAAGCGATCC | 55666 |
rs374372594 | snp | C/T | 0.000773221 | 0.0196472 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613473 | AAGGCTCGAGGGAAA[C/T]AGGAACAACAAATCG | 55666 |
rs374388145 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570183 | CCTTCATGGGCAAGC[A/G]GCGGGGTGGGTCATG | 55666 |
rs374422690 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605978 | GGCGCCCATCACTAC[A/G]CCCAGCTAATTTTTT | 55666 |
rs374465538 | snp | A/G | 2.53611e-05 | 0.00356088 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572005 | CCCAAGCTGTGCATG[A/G]GGGGCACTTACGTCT | 55666 |
rs374539192 | snp | A/G | 0.000157988 | 0.00888644 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610292 | AGAAAAAGGCAGAGC[A/G]GTGAGGATGTCTGTG | 55666 |
rs374544964 | snp | A/G | 0.000161987 | 0.00899817 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559454 | GCACTCATCATTTCT[A/G]GCCCACCAGAGACTG | 55666 |
rs374560692 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564737 | AGGTTGCAGTGAGGC[A/G]AGATCACGCCACCAC | 55666 |
rs374586287 | snp | C/T | 0.000266095 | 0.0115315 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596280 | TCAAATTTTACAGCA[C/T]CATGCCAAAATATAC | 55666 |
rs374665540 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620916 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCTGA | 55666 |
rs374677358 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614925 | GAGGGCAGGATCCAC[-/A]GCTCTAAACCAACAC | 55666 |
rs374709941 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589597 | AGACCTAGCACAAGA[C/T]CTAGCACAGTCAGGA | 55666 |
rs374727447 | snp | A/G | 0.00138489 | 0.0262779 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559228 | GAAGGGCTGGGCTGG[A/G]CCCGGTCCTAGCCAG | 55666 |
rs374786782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629480 | GGTGTGAGCCACCAC[A/G]CCCAGCCGTGAAATA | 55666 |
rs374803495 | snp | A/G | 1.65636e-05 | 0.00287776 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613365 | GTCCTGTTTGCTGAG[A/G]TACTGATCAATCTCA | 55666 |
rs374808635 | snp | A/G | 0.00017811 | 0.00943522 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81565581 | ATTTCTGGTCCGCAC[A/G]GCCTCCAGCAGCAAG | 55666 |
rs374897119 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620557 | GGGAAGCTTCTGCAG[G/T]GGCTGCCAATGCCTT | 55666 |
rs374948564 | snp | A/C | | | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563858 | AAACTAATGCAGGAA[A/C]AGCAAACCAAATACT | 55666 |
rs374971081 | in-del | -/TG | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558906 | ATAAAGAGAAGGCTG[-/TG]GGTGGTGGCAGCATC | 55666 |
rs374991652 | snp | A/C/T | 0.00029948 | 0.0122334 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606742 | AGTACAGATGCCATT[A/C/T]GGCCACGGGAGGTGC | 55666 |
rs375006840 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594711 | ACCCGGGAGGTGGAA[C/G]CTGCAGGGAGCCGAG | 55666 |
rs375021905 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616314 | CGACATAGCAAGACT[A/C]TGTCTCAAAAAAAAA | 55666 |
rs375049637 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616257 | ACCCAGGAGGCGGAG[C/G]TTGCAGTGAGCTGAG | 55666 |
rs375092141 | in-del | -/A/AAA | 0.31357 | 0.241783 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586607 | GAGCAAAACTGTCTC[-/A/AAA]AAAAAAAAAAAAAAA | 55666 |
rs375129128 | snp | A/G | 2.26863e-05 | 0.00336788 | missense, nc-transcript-variant, synonymous-codon | NPLOC4 | GRCh38.p7 | 17:81559387 | CGGCGCCGTACTCAT[A/G]GAGACCTGGGAGCTG | 55666 |
rs375129514 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617662 | AAAACACAAAAAATG[-/C]CCCCCCTCCCCCTCC | 55666 |
rs375198669 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634709 | CCCTCCCTCAACCTC[A/C]AGAGTAGCTGGGATA | 55666 |
rs375232636 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629433 | CACTTCGTGATCCAC[A/C]CGCCTTGGTCTCCCG | 55666 |
rs375263256 | snp | C/G/T | 0.000728362 | 0.0190705 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588901 | CAAGACAGGTTCACA[C/G/T]CATTCTCCATGTACA | 55666 |
rs375264307 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595534 | ACATATATATATATA[-/T]TTTTTTTTTTCTTTT | 55666 |
rs375331653 | snp | A/G | 0.000165986 | 0.00910855 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604752 | TAACAAGAGTGGGCT[A/G]ATGAAAACATGCCAT | 55666 |
rs375389977 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634903 | ATTTTTCAAAGGAGT[C/G]AAAGGTTTCTTGGCC | 55666 |
rs375402063 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621007 | CAGCCTGGGTGACAC[A/G]GTGAGATTCTGTCTC | 55666 |
rs375405901 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607367 | GAACTTTTTCTTTTT[A/C]TCCAGCTTTATTGAA | 55666 |
rs375412180 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603032 | ATAAAAGTCAGACAT[-/G]GTGGTGCACGCCTGT | 55666 |
rs375438037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620985 | CTACGATCGCACCAC[C/T]GCACTCCAGCCTGGG | 55666 |
rs375439242 | snp | A/G/T | 8.33401e-05 | 0.00645476 | missense, upstream-variant-2KB, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613432 | CCCGGTGGAACTGAC[A/G/T]TCTCCATTTCAGATG | 55666 |
rs375557101 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589780 | GGGCGGGAGGACTGC[C/T]TGAGCCCAGGAGTTT | 55666 |
rs375603233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571855 | CGCATGCTCAGTGAT[C/T]CTACAACCACCTCCT | 55666 |
rs375608281 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623729 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 55666 |
rs375662739 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595427 | TGACAGTAAGACTGT[C/G]AAAAAAAAAAAAAAA | 55666 |
rs375715761 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617118 | CATGTCTCACAGCCC[A/G]GATAGGGAGTCCTCA | 55666 |
rs375720898 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616846 | GAGACCGAATATCAA[-/C]CTCTACATGGGATAT | 55666 |
rs375745772 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582976 | GGCCAGGCCTCCTCC[C/T]TGCGGCGCCGCCCCT | 55666 |
rs375906808 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600975 | CGATGAGCTCACCAA[C/T]CCTAAGGAAGGGAAA | 55666 |
rs375912622 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571280 | AGCCGCCTCCCGTCC[A/G]CTTTGGACAGAGCTC | 55666 |
rs375952331 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620972 | AGGCTGCAGTGAGCT[A/G]CGATCGCACCACCGC | 55666 |
rs376067795 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591884 | AGATCCCCAGCAAGT[A/C]ATTTTAACAGCCCGT | 55666 |
rs376072453 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630990 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 55666 |
rs376125584 | snp | A/G | 3.75129e-05 | 0.00433071 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600299 | TGGATGCCCAACAGA[A/G]CCTGGCCACGCCCCC | 55666 |
rs376163103 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626064 | TGAAACAGGAGAATC[G/T]CTTGAACCTGGGAGG | 55666 |
rs376181584 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620989 | GATCGCACCACCGCA[C/T]TCCAGCCTGGGTGAC | 55666 |
rs376232939 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568304 | CGGACATCTTCAGCA[C/G]AACCAAACACAGAGC | 55666 |
rs376275967 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596442 | CCAAAACCTGGTCTC[C/T]ACTAAAAATAAAAAA | 55666 |
rs376281316 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592758 | TGAGGCCGAGACAGG[C/T]GGATCACTTGAGGCC | 55666 |
rs376323005 | snp | A/G | 3.31279e-05 | 0.00406975 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596170 | CGTCTGGAGAGAGCC[A/G]GCACATGTTGGGATG | 55666 |
rs376338396 | snp | G/T | 6.63713e-05 | 0.00576032 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81569019 | CAAAGAGCTCACCTG[G/T]GTCTCACCCAATACA | 55666 |
rs376351128 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587360 | TTGCTCTGTCACCCA[A/G]GCTGGAGTGCAGTGG | 55666 |
rs376440812 | snp | A/G | 2.68302e-05 | 0.00366256 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567369 | CACAGGCGTCTCTTT[A/G]CAGCCAAAGCCCACT | 55666 |
rs376447528 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636734 | GAGGGACACGGACGG[A/G]AAGCAGCCGAGGGGG | 55666 |
rs376456668 | snp | A/G | 0.488965 | 0.0734569 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618643 | GGGGCGCCTCTGCCC[A/G]GCCGCCCCTACTGGG | 55666 |
rs376481116 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594839 | TAGTCCCAACTACAT[A/G]GGAGGCTGTTGGGGT | 55666 |
rs376488586 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575618 | AATCGGCAAGGACAG[A/C]TGGACAGCTGTGTAG | 55666 |
rs376555585 | snp | C/T | 8.28219e-05 | 0.0064346 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596155 | TGGATCCAAAATGTC[C/T]GTCTGGAGAGAGCCG | 55666 |
rs376620862 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611833 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 55666 |
rs376640033 | snp | G/T | 0.000248589 | 0.011146 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629844 | TTACTGCACAGCCTA[G/T]TGAGGTCCTGATCTA | 55666 |
rs376645574 | in-del | -/GTT | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638301 | AGTTTTTTGTTTTTT[-/GTT]TTTTTTTGTTTTTGA | 55666 |
rs376812039 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627508 | ACTTTGGGAGGCCAA[A/G]GCGGGTGGATCACCT | 55666 |
rs376896529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560630 | GAGAATGGCGTGAAC[C/T]TGGGAGGCGGAGGTT | 55666 |
rs376904361 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628801 | AACTGTCATGGGAAT[C/T]CTGGACACAATGCAG | 55666 |
rs376910768 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614744 | GACCTCAGAGGCTAA[C/G]AAGCATCTCCACTCA | 55666 |
rs376915553 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596467 | AAAAAAATTATCTGG[C/G]TATGGTGGTGCACAC | 55666 |
rs376951108 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560192 | GGAGGCCGAGGCGGG[G/T]GGATCACTTGAAGTC | 55666 |
rs376990575 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611302 | TCCAGCCTGGGAGAC[A/G]AGAGTGAAATTCCAC | 55666 |
rs376992052 | snp | A/C/T | 0.000253114 | 0.0112474 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81600357 | TTCCGCAGGCCAAGT[A/C/T]TGGCAGCAATTTCAT | 55666 |
rs377051420 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593399 | CTGTGCTGTCCTCAC[A/G]AGTCAGTCCAGAAGC | 55666 |
rs377107698 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568250 | TCTCCATCTAGGGCA[A/G]CAAGAGGGAGGAATG | 55666 |
rs377130166 | snp | A/G | 1.65864e-05 | 0.00287974 | synonymous-codon, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81589045 | ACTCATCACGGACCA[A/G]TGCCATACACTGATT | 55666 |
rs377147194 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632898 | AAAGGCTCCACCCAA[C/T]ATGTTCTCAACTTTT | 55666 |
rs377206783 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633127 | AGCAAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 55666 |
rs377226420 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624851 | AAAGACCAGGAGGCA[C/G]GAAGGGTGTTGGAAA | 55666 |
rs377249613 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598763 | TGTCACTTCTGTCCT[C/T]GGGAAGGATCTGCGG | 55666 |
rs377263247 | snp | A/G | 0.000350693 | 0.0132372 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571972 | TCCCACCTACAAGGC[A/G]CCCAATGGGTCCACC | 55666 |
rs377264812 | snp | C/T | 4.84508e-05 | 0.00492169 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613518 | ATGATAAACAGAGGC[C/T]GATGCCTTCCCTTAC | 55666 |
rs377268956 | snp | C/T | 0.000161987 | 0.00899817 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567486 | GATGGTATCCAAGAA[C/T]ACAGATGAGGTATTC | 55666 |
rs377309785 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616282 | GCTGAGATCGCACCA[C/T]TGCACTCCAGCCTGG | 55666 |
rs377325024 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607732 | ATCAATCTGCACCCA[A/C]TCCTTAGTCCAGAGA | 55666 |
rs377352359 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570240 | CGGCTACATGGCCTC[A/G]TCAGTTAGGGATCCT | 55666 |
rs377354939 | snp | A/C | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577516 | GGGTTAGCTCAACGC[A/C]CTCTTCTCTTCTCCC | 55666 |
rs377356784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635047 | AAAATGTTTTTAATT[A/G]AAAAGATTTAAAGGC | 55666 |
rs377378349 | snp | C/G/T | 5.3813e-05 | 0.00518692 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606842 | GAAGCAACTTAAACA[C/G/T]CACATTGGTGAAAAG | 55666 |
rs377415208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587487 | TGCCCGGCTAACTTT[C/T]TGTAGTTTTAGTAGA | 55666 |
rs377466373 | snp | C/T | 0.000309443 | 0.0124349 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604566 | AGGTGGCTCATAAAT[C/T]GCAGCCACTTCAGCC | 55666 |
rs377467231 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635308 | CGCACCACTGAACTC[A/C]AGCCTGGGCGACAGA | 55666 |
rs377534388 | snp | C/T | 0.000157988 | 0.00888645 | missense, intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81608764 | TTCCGGATGTAGGCG[C/T]GGAAGGACATGTGCT | 55666 |
rs377542390 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628983 | TCCTGGGTTCACATC[A/C]TTCTCCTGCCTCAGC | 55666 |
rs377553744 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620978 | CAGTGAGCTACGATC[A/G]CACCACCGCACTCCA | 55666 |
rs377592776 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618545 | GAGGTGAGGGGTCAG[-/T]GCCCCCGCCCGGCCA | 55666 |
rs377608804 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638278 | GTCCTTGAGAATTCA[-/G]GGATCAGAGTTTTTT | 55666 |
rs377643942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569650 | TGGGAGCCACTCCAC[A/G]GAGCTGTGGGCTTTT | 55666 |
rs377723409 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631878 | AATCTTGGCTCACTG[A/C]AACCTCTGCCTCTTG | 55666 |
rs377750433 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573758 | AATAGATCCCACTGA[G/T]GTTTCCAGGAGGGCA | 55666 |
rs377761235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604845 | TAAAAAACAAACCAA[C/T]AGGGTGTGATGGTGC | 55666 |
rs386386774 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637947 | CAAAAAAAAAAAAAA[-/AAA]AAGACGTCACTTCAC | 55666 |
rs386627318 | in-del | -/ACAT/AT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603014 | CACACACACACACAC[-/ACAT/AT]ATATAAAAGTCAGAC | 55666 |
rs386627320 | in-del | -/TACTGC | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614598 | AGTCAGACTTAAGGG[-/TACTGC]TTTCCAAAAAGGTTG | 55666 |
rs386799900 | multinucleotide-polymorphism | AGT/GGC | | | cds-indel, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558983 | AGGTCTTTCCAACAC[AGT/GGC]GGGGGACTTGTCAAC | 55666 |
rs386799901 | in-del | AAT/GG | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563170 | AACCTACGCTTCCTG[AAT/GG]TCAAGTGATTCTCCT | 55666 |
rs386799902 | multinucleotide-polymorphism | CA/TG | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563177 | GCTTCCTGGGTCAAG[CA/TG]ATTCTCCTGCCTCAG | 55666 |
rs386799903 | multinucleotide-polymorphism | AC/GT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564703 | TGAGGCAGGAGAATC[AC/GT]TTGAACCCAGGAGGT | 55666 |
rs386799904 | multinucleotide-polymorphism | AG/CA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564712 | AGAATCGTTTGAACC[AG/CA]GGAGGTGGAGGTTGC | 55666 |
rs386799905 | multinucleotide-polymorphism | GA/TT | | | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564986 | GCAGCAATGCTGACA[GA/TT]AGGTTCTCACGAGTG | 55666 |
rs386799906 | in-del | AAAGAACGAAAACCTGGCGTG/CCTGT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576634 | CTTTGTATAAAAGAC[AAAGAACGAAAACCTGGCGTG/CCTGT]TGTTTGCAACACACG | 55666 |
rs386799907 | multinucleotide-polymorphism | AT/GC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616303 | TCCAGCCTGGGCGAC[AT/GC]AGCAAGACTCTGTCT | 55666 |
rs386799908 | multinucleotide-polymorphism | CAT/TAC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616445 | TGTAGAAGAGTAACA[CAT/TAC]GGGCCAGGCACAGTG | 55666 |
rs397699904 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634456 | AGTGGGAAAAAAAAA[-/A]ATGGCCTTGTCTGAA | 55666 |
rs397747470 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626330 | AAGAAAAAAAAAAAA[-/A]GAAAAGAATGAAAAT | 55666 |
rs397765936 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634457 | GTGGGAAAAAAAAAA[-/A]TGGCCTTGTCTGAAA | 55666 |
rs397774435 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638056 | TGTGACAGTTTTTTT[-/T]AAACTATGTTAAATT | 55666 |
rs397774490 | in-del | -/TTAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606838 | AGAGAAGCAACTTAA[-/TTAA]ACATCACATTGGTGA | 55666 |
rs397790286 | in-del | -/CT | 0 | 0 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635929 | AGGGACTGGTTTTCT[-/CT]GATTTGTCACTGATA | 55666 |
rs397799791 | in-del | -/G | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626919 | CATAGTGAAACCTCG[-/G]TCTCTACTAAAAATA | 55666 |
rs397856479 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609055 | CTCACTCTGTCGCCC[-/C]AGGCTGGAGTGCAGT | 55666 |
rs397857390 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634605 | TTTTTTTTTTTTTTT[-/T]GAGACAGTCTTGCTC | 55666 |
rs397857926 | in-del | -/GTT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595955 | TTATGCTGTTAAGTT[-/GTT]CAGAATTTTTACCAT | 55666 |
rs397955892 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634051 | GTATTTTTTTTTTTT[-/T]AGTAGACGTGGGGTT | 55666 |
rs397956783 | in-del | -/AA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633144 | AAAAAAAAAAAAAAA[-/AA]GAAAAGAAATACAAT | 55666 |
rs398031763 | in-del | -/A | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619218 | AAAAAAAAAAAAAAA[-/A]CACAAAAAATTAGCC | 55666 |
rs398058956 | in-del | -/GTT/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595957 | TTATGCTGTTAAGTT[-/GTT/T]CAGAATTTTTACCAT | 55666 |
rs527271613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586565 | CAGTGGGCCGAGATC[A/G]CGCCACTGTACTCCA | 55666 |
rs527286236 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592438 | TGAGCACCAAGAGGG[A/G]TGATTCACACAGACA | 55666 |
rs527312750 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622761 | TCACCATGTTGGCCA[C/T]GGTGGTCTCAAACTC | 55666 |
rs527348756 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623967 | CCATTCTGGGTGTTC[A/G]GATCACAAAAATGAA | 55666 |
rs527389650 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633003 | GGCGTGGTGGAGGGC[A/G]CCTGTAGTCCCAGCT | 55666 |
rs527409371 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581682 | TATACTCCCGGGGCG[C/G]CAGCCAGCAAGGTGG | 55666 |
rs527436058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575822 | GGGAAGATGCAAAAT[G/T]TTCTCTTAAGACTGG | 55666 |
rs527491474 | in-del | -/AC | 0.177365 | 0.239216 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574880 | CAAACAAACAAACAC[-/AC]ACACACACACACACA | 55666 |
rs527497834 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582202 | TTGTCCTGCAGGCTG[A/C]AGCAGCACAACCAGG | 55666 |
rs527531355 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616040 | CTGCTAAATCTGGGC[C/G]GGGCGTGGTGGCTCA | 55666 |
rs527559685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565162 | GACCAAAAGGTCCCA[C/T]GCTTCCGGCGCTTCC | 55666 |
rs527561599 | snp | A/G | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610901 | AGCTTGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 55666 |
rs527566763 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566157 | GCAAACGTGGCGAAA[C/T]CCCGTCTCTACTAAA | 55666 |
rs527593332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610374 | TGCCCACGTGGAGTT[A/G]TATTCCAGATGGCAC | 55666 |
rs527612197 | snp | C/G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585662 | GAAGACTCCATTTCT[C/G/T]GGGGGGGGGGGAAAG | 55666 |
rs527627681 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557626 | ATCTCAGGACCAGAG[C/G]AGACAGCAGAGGACA | 55666 |
rs527632079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576308 | GAATTACAGTTGGCC[A/G]TTGCACAACGCGGGT | 55666 |
rs527641088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574589 | TATCTCCACCTGGAG[C/T]GAGGCACCAGGAGGT | 55666 |
rs527647143 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577829 | TCCAAACCTCTCAGT[C/G]CCAGCACACCATCCT | 55666 |
rs527757164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608900 | CTCTGCTACGCACAG[C/G]GGGAGGCCAGCAGCA | 55666 |
rs527773373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569420 | TTCCCTTCAGAGTCA[C/T]ACAGGTTCTCTCCCT | 55666 |
rs527773890 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560187 | CTTTGGGAGGCCGAG[A/G]CGGGTGGATCACTTG | 55666 |
rs527809533 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580014 | CCTCCTCTCCTGACT[C/T]ACCAGGGAGCTCCTT | 55666 |
rs527828122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575094 | ACAAAGCTTTCAGAC[A/C]CTCGGTTACTTTTCT | 55666 |
rs527856710 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635765 | GTCACAATGCTACAG[C/T]ATGAACATTACTCTT | 55666 |
rs527864080 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595784 | CCTGACCTCAAGCGA[C/T]CCACTCACCTGGGCC | 55666 |
rs527874239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603656 | TTTAAAGAATTTTAC[A/T]GTGAATACTCATATA | 55666 |
rs527923024 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602966 | ATATATATACACACA[C/T]ATATATACACAAATA | 55666 |
rs527939433 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562020 | AGGTGGATCACCTGA[A/G]GTCAGGAGTTCCAGA | 55666 |
rs527946769 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597523 | GGTGCGGTGGCTCAC[G/T]CCTGTAATCCCAGCA | 55666 |
rs527992687 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559080 | CCAGCCGTGGCGCCC[A/G]CTCTCCAGGGAGGAA | 55666 |
rs528063135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568289 | AGCCGTGATGCAGCA[C/T]GGACATCTTCAGCAG | 55666 |
rs528074423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601276 | TGAAAATCTGGCAAA[A/C]CACAAAGAAGTTTAC | 55666 |
rs528135728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600730 | AGGTCTACACACTCT[A/G]CCTGTTTTAAAAGTT | 55666 |
rs528161520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596041 | ACTAAGTTAAGGATA[A/G]AAAGCTACCAAAAAG | 55666 |
rs528168543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628496 | CCAGCCTGGGCAACA[A/G]AGTGAGATGCCATCT | 55666 |
rs528173531 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573387 | TCTTCTGAGACAATC[A/T]TCACAAGCTGTTCCC | 55666 |
rs528183742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562946 | CTGTCTCAAAAAAAA[A/G]AGGAGGGGGGAAAAA | 55666 |
rs528206457 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634649 | GGAGTGCAGTGGCGC[A/C]ATCTGGGCTCACTGC | 55666 |
rs528251021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629014 | CTCACCAGCAGCTGG[A/G]ACTACAGGTGCCCGC | 55666 |
rs528278874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590556 | TTACTATGTTACCCA[A/G]GCTGGTCTCTAACTC | 55666 |
rs528284259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591059 | TGACACTGAAAGAAT[A/G]CAGGGCTCAGAGGGA | 55666 |
rs528299701 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558923 | GTGGTGGCAGCATCG[A/G]CCCCTCCCTGTGCGC | 55666 |
rs528378411 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618869 | GTACTAAGAAAAATT[A/C]TTCTGCCTTGGGATC | 55666 |
rs528408688 | in-del | -/G | 0.0154538 | 0.0865337 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619473 | GAATCGCTTGAACCC[-/G]GGGGGGGCAGAGGTT | 55666 |
rs528441784 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596393 | CGGGAGGTCCACTTG[A/G]GGACAAGAGTTCGAG | 55666 |
rs528471794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589252 | TGTTCAGTAGTCGGC[C/T]GGGTGCGGTGGCTCA | 55666 |
rs528483597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594754 | CACTCCAACCTGGGC[A/G]AGAGCGAGACTCCGT | 55666 |
rs528502588 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614244 | ATCACACCACTGCAC[C/T]CCAGCCTGGTGACAG | 55666 |
rs528525036 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558023 | CCCGTGGGTGCAGAG[C/T]AGCCCAGATGTGGCC | 55666 |
rs528546797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617329 | CCCAGCTGCAGTGCA[A/G]TGGCACAATCACAGT | 55666 |
rs528548607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623149 | CAGGGAGCCGAGATC[A/G]TGCTATTCCACTCCA | 55666 |
rs528608201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627862 | AACTGCTGGAACCCA[C/G]GAGGCGGAGGTTGCA | 55666 |
rs528629971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583737 | CCTCGTTCTCTTACT[A/G]GCTGCATATGGGACA | 55666 |
rs528690907 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627915 | CATTCCAGCCTGGGC[A/G]ACAGAAAAAGACTCC | 55666 |
rs528707164 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617810 | ATTGCAGGCGCGCGC[C/T]GCCACGCCTGACTGG | 55666 |
rs528749756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607013 | CCGAATCCCAGCTTC[C/T]GTCCCACATACTTCA | 55666 |
rs528768815 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573834 | GCCCCATCAAAGGCT[A/C]CATTCCTGCAAATAC | 55666 |
rs528777073 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589455 | AATGGCGTGAATGGC[A/G]TGAACCCGGGAGGTG | 55666 |
rs528821567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582996 | GCGCCGCCCCTGCGC[A/G]CTCACAACTGAGCGC | 55666 |
rs528833240 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573409 | GCTGTTCCCAAGTCA[A/C]ACCAAGTCCATTACC | 55666 |
rs528842686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576530 | TGTGTCAACTGAGGG[C/G]CAATTGTACTTCCAA | 55666 |
rs528928357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616485 | CCTGTAATCCCAGCA[C/T]GTTGGGAGGCCGAGG | 55666 |
rs528941589 | snp | C/T | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636003 | TTTGAGACGCAGTCT[C/T]GCTCTATAGCCCAGG | 55666 |
rs528949749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611732 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACAAGTC | 55666 |
rs528963092 | snp | C/T | 0.000105551 | 0.00726391 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572112 | GTCAGAGGGGAACAG[C/T]GGTGAGCAAAGACGA | 55666 |
rs528985473 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616662 | GTGAACCCAGGGGGC[A/G]GAGCTTGCAGTGAGC | 55666 |
rs528990771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611319 | GAGTGAAATTCCACT[C/G]AAATAAATAAATAAA | 55666 |
rs529032829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571727 | CCTAGCCTGGGGTCA[C/G]TGGTCCTTTGTACTT | 55666 |
rs529036016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599303 | AAAAAAAAAATAAAA[C/T]AAAATAAAAAGAGAA | 55666 |
rs529046586 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606214 | TCTCTCTAAGGAGCC[A/G]TTTTCTCTAAGGGCA | 55666 |
rs529065468 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620064 | CTCTACAGGTCAATG[A/G]ACCAAGTTCCTCAAC | 55666 |
rs529070773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566279 | GGAGGTTGCAGTAAG[C/T]CAAGATTGCGCCAAT | 55666 |
rs529072983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638479 | AATTTTGTATTTTTC[A/G]TAGAGACGGAGTTTC | 55666 |
rs529084167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605642 | TACGGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA | 55666 |
rs529084445 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620830 | TTAGATAATGGTTAC[A/G]TGTTCCAGATTTAAA | 55666 |
rs529101093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584575 | GAGTGCTGTTTGGGA[A/G]ATCCCAGGCAACACT | 55666 |
rs529157802 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601956 | CTGCCTCCCAGGCAG[A/G]TTATCTAAATAGGAG | 55666 |
rs529193946 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617631 | TGGCTAACACGGTGA[C/G]ATCCCGTCTCTATTA | 55666 |
rs529197963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566681 | CTGACAGAGAAAGGC[C/T]GGGGGAGGAGGAGCC | 55666 |
rs529221509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564798 | CGTCTCAAAAAAAAA[A/G]AAAAAAACAGGAAAT | 55666 |
rs529224103 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632908 | CCCAATATGTTCTCA[A/C]CTTTTAAGTCAGGAG | 55666 |
rs529240694 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628027 | ACCATCCTGGCTAAC[A/G]TGGTGAAATCCCGTC | 55666 |
rs529242898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570721 | TGCCTGCCCAGCCAT[C/T]CCATCCCAAGGTTTA | 55666 |
rs529252429 | snp | C/T | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556644 | AGAGGCACCCAAGGG[C/T]GGCGGGGCCGTCAAA | 55666 |
rs529338135 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615429 | TAATAGCAGATTACA[A/T]ATTCCTAAACACCAT | 55666 |
rs529358391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598330 | TTTCCTCAGCACCAG[C/T]TCTGCCCAGCACCAT | 55666 |
rs529363258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595768 | AGGCTGATCTCGAAC[C/T]CCTGACCTCAAGCGA | 55666 |
rs529370059 | in-del | -/AAA | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635373 | AAAAAAAAAAAAAAA[-/AAA]GGAGTCGACGTTTCC | 55666 |
rs529374964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616622 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 55666 |
rs529386517 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631086 | GCTGAGGCAGGAGAA[A/T]CGCTTGAACCCAGGA | 55666 |
rs529425991 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637107 | TCCCGGTGCCTCGCT[C/T]AATACGCTCCCCTCG | 55666 |
rs529427687 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631817 | ATTTTTTTTTTCCCC[A/G]AGATGAAGTTTCAAT | 55666 |
rs529460860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593622 | AGTCTGATAGGCTTG[A/G]AAACTACCAGCCTAC | 55666 |
rs529470001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625802 | GGCAGAGATTTGGGG[A/G]AAAAAAAAACAGCCT | 55666 |
rs529477547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560116 | TGTTTTTATTTCTCT[C/T]GGATAAAAACAAAGA | 55666 |
rs529520401 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598764 | GTCACTTCTGTCCTC[C/G]GGAAGGATCTGCGGC | 55666 |
rs529526938 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558924 | TGGTGGCAGCATCGG[-/C]CCCTCCCTGTGCGCC | 55666 |
rs529563196 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558108 | GCCCCGGCCTGGCCA[C/T]GCCACAGAGGAACGC | 55666 |
rs529575432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587918 | CTGACCTTGTGATCC[A/G]CCCATCTCGGCCTCC | 55666 |
rs529595408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621417 | ACAGCCAACTGCCAG[C/G]AGGTCCCAGGCCCAC | 55666 |
rs529595642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629604 | TGATAGAGAAAGGCA[A/G]TGCAAGAGGCAATTT | 55666 |
rs529635856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626346 | GAAAAGAATGAAAAT[A/G]GAACAGAAAAATACT | 55666 |
rs529661606 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559075 | GAATACCAGCCGTGG[C/T]GCCCGCTCTCCAGGG | 55666 |
rs529702722 | snp | C/T | 3.31631e-05 | 0.00407191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597208 | CCATCTGTAACCAAG[C/T]CATAGGGCCACACGC | 55666 |
rs529709268 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624190 | CTCTGGGAGGCCGAG[A/G]TGGGCGGATCACGAG | 55666 |
rs529717108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593996 | AAATCTGACTCGGCC[A/G]GGCGCAGTGGCTCAC | 55666 |
rs529733008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619476 | ATCGCTTGAACCCGG[C/G]GGGGCAGAGGTTGTG | 55666 |
rs529749848 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625473 | ATCTCGGTAAAGAAA[C/T]AAATCATAAAAGAAC | 55666 |
rs529749898 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605205 | AGAATGGCGTGAACC[C/T]GGGAGGTGGAGCTCG | 55666 |
rs529754980 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624695 | TCGAAATAAGCACTA[C/T]GACAGAAAAGGAAAA | 55666 |
rs529788267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585945 | AACAAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 55666 |
rs529853075 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586074 | TAGGTCACTTGAGAT[C/T]AGGAGTTCGAGACCA | 55666 |
rs529933212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581182 | TGGCGAAACCCTGTC[A/G]CTACTAAAAATACAA | 55666 |
rs529938935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586524 | CTGAGGCACAAGAAT[C/T]GCTTGAACTCAAGGG | 55666 |
rs529940906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620294 | CGAGGTCAGGAATTC[A/G]AGACCAGCTTGGCCA | 55666 |
rs529973119 | in-del | -/CTC/CTG | 0.00279258 | 0.0372817 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558903 | AAAATAAAGAGAAGG[-/CTC/CTG]CTGGGTGGTGGCAGC | 55666 |
rs529984849 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570150 | GAGCCACCAGCAGCA[A/T]CTCTGGCCTGAGCTG | 55666 |
rs529996124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585453 | CAGATCACGAGGTCA[A/G]GAGTTTGAGACCATC | 55666 |
rs530005166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615478 | AACTTGACTTACACA[A/C]AAGATCAATTTTAAC | 55666 |
rs530047205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575440 | ACTTAGAAAATAGTC[C/T]AGTCCGTGTGCAACG | 55666 |
rs530054254 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563032 | GCAGGAAGATCACTT[A/G]AGCCTAGGAGTTTGA | 55666 |
rs530119627 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563640 | GCATCAAAGGGCTGG[A/G]TGCAGTGGCTCCCAG | 55666 |
rs530132859 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632699 | TCCTCTTCAACCATT[A/G]TGCAGATGAAAACTG | 55666 |
rs530140157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613705 | GTTCTCTGTAATTTA[A/C]TCTCTTACAACTTTA | 55666 |
rs530159550 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624196 | GAGGCCGAGGTGGGC[A/G]GATCACGAGGTCAGG | 55666 |
rs530192315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574544 | TTGTCTTAATTCTAA[A/G]TTTGGCAGCCGTCAA | 55666 |
rs530216270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618800 | TTGAGAAATCGGATG[A/G]TTGCTGTGTCTGTGT | 55666 |
rs530221383 | snp | A/G | 0.000884624 | 0.0210126 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608844 | AGACACAGAGTAAGC[A/G]AGTGCAGTCTCACAC | 55666 |
rs530259003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608381 | GGCCACGCAGCCAGG[A/C]GCCTGCACAGTCGCT | 55666 |
rs530259678 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580079 | CCTCCTCCCCAGCTC[C/G]TGCCTCCCAGTGCTC | 55666 |
rs530264598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590595 | ATGTGATCCTCCTGC[C/G]TCAGCTTCCCAAAGA | 55666 |
rs530284233 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564801 | CTCAAAAAAAAAAAA[A/C]AAAACAGGAAATGGT | 55666 |
rs530286668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568989 | AGCAGTTACCTTAAA[A/T]TATGTTTCTAAAGAC | 55666 |
rs530301353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596972 | AAAAAAATTAGCTGG[A/G]CATGGTGGCAGGCGC | 55666 |
rs530344529 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635028 | AGACCTCATCTCTAT[-/A]AAAAAAATGTTTTTA | 55666 |
rs530381560 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566880 | CCCCCACTACCCAGA[C/G]CAGCCACTTCTGCAA | 55666 |
rs530440589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572715 | CACTCAGGCGCGATC[A/T]GCGACAGGCAGAAGG | 55666 |
rs530478380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573341 | CCCCATCACAACCAC[A/G]CCTTCCTGGGGATGT | 55666 |
rs530508734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606911 | TACCTCCTGAACAGT[A/G]TCTCAGGAGCTAAGC | 55666 |
rs530544802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578354 | CGCACCCTGCTCCCC[A/G]ACAGGACACCTCCAC | 55666 |
rs530547847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606300 | ACATCCAGAAAGGCC[A/G]GAACGCTCCCTCCTT | 55666 |
rs530562256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567815 | GGCCAGGTGTGGAGG[C/T]TAACACAGTAATTCC | 55666 |
rs530586420 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562743 | CAAGAGTTCAAGACC[A/T]GCCTGGGCAACATAG | 55666 |
rs530590091 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558391 | TGCTCCTGCTCAGCC[C/T]GCAGTATCTGCAGTT | 55666 |
rs530627446 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595249 | GATTAGCCTGGCCAA[C/G]AAGGCAAAACCCAGT | 55666 |
rs530668692 | in-del | -/AA/AAA | 0.461813 | 0.132798 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613127 | AACTGATAAAAAGCT[-/AA/AAA]AAAAAAAAAAAACAA | 55666 |
rs530679033 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634552 | TTTCAGTGCTAATTC[C/T]TAACCTATTTCTAGG | 55666 |
rs530731883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595840 | TGAGCCACCACGCCC[A/G]GCCAAAAAAGTGGAC | 55666 |
rs530764605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632749 | AAAGATTTCCACTGA[C/T]ACAGGACAAAACACC | 55666 |
rs530809873 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594200 | AAATGGCGTGAACCC[A/G]GGAGGTGGAGCTTGC | 55666 |
rs530838340 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581281 | TTGAACCTGGGAGGC[A/G]GAGGTTGTAGTGAGC | 55666 |
rs530840000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628426 | GGCTTAGGCAGAGGA[C/T]TGCTTGAACCCAGGA | 55666 |
rs530841734 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558703 | GGGCAGGCAGCAAAC[C/T]GACCTGCAGACCTGC | 55666 |
rs530865781 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609590 | GTCGGGACTACAGGC[A/G]TCACTGCACATAGCC | 55666 |
rs530893250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627429 | GGTGGGGAACAAAAA[C/T]GAACTGTCAACTCAG | 55666 |
rs530906357 | in-del | -/A | 0.106987 | 0.205054 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623798 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAACAAAA | 55666 |
rs530925329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627050 | AGGCAAGATTGTGCC[A/G]CTGCACTCCAGCTTG | 55666 |
rs530925456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633637 | AGTTTCCCTATTTAT[A/G]AGAAAATAAGACTAG | 55666 |
rs530998862 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594692 | AGGCAGGAGAATTGC[A/G]TGAACCCGGGAGGTG | 55666 |
rs531015400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622114 | AACCTCGGGCAGATC[A/G]TGGGGACCTCATTTC | 55666 |
rs531035988 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594981 | AAAACACAAAAACCC[A/G]GCAAACTCAAGAATA | 55666 |
rs531044389 | in-del | -/T | 0.166832 | 0.235761 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634039 | GGTTAATTTTTTGTA[-/T]TTTTTTTTTTTTAGT | 55666 |
rs531062831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588733 | AAGCCAGTGCATGTA[C/G]CTCCACTTCTGGTGA | 55666 |
rs531112374 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617263 | TAGGGGGAAAAAAAA[A/T]CAGATTACGTATTTA | 55666 |
rs531116746 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583637 | CCTAAAAAACTACAC[A/G]TGAACGATGACACAA | 55666 |
rs531157735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583120 | TTCTTCCTAATTATC[A/G]AGAGAGATGTTAGTG | 55666 |
rs531194970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612423 | CAAGCAAGCCAGTGC[C/G]AGGCCCCTGGGAGGA | 55666 |
rs531197224 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587793 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 55666 |
rs531198297 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617796 | GCCGAGTGCCTGCGA[C/T]TGCAGGCGCGCGCCG | 55666 |
rs531227939 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571476 | CCACCCAGTAAACCA[C/T]GCTGAGCCCTCACTC | 55666 |
rs531232235 | snp | C/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637690 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCA | 55666 |
rs531269519 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621013 | GGGTGACACGGTGAG[A/T]TTCTGTCTCAAGAAA | 55666 |
rs531306041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616149 | CAGTGAAACCTCGTC[G/T]CTGCTAAAAATAAAA | 55666 |
rs531326129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582232 | GAGGGCCGTGAGGTA[A/C]GCGAGCTGTGGCATG | 55666 |
rs531377899 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626242 | AACCGCTTGAACCCC[A/G]GAGGCGGAGGTTGCA | 55666 |
rs531424126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576416 | GAAACTCATGTATAC[A/G]GAGGTCTAACTTTAC | 55666 |
rs531428532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611233 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCTGGGA | 55666 |
rs531452712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605459 | AACCTCAAAAATTAT[C/T]CAATACAGTGAAACC | 55666 |
rs531490508 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571603 | AAGCACCTGCACGTG[C/T]AGGACAGCTGACAGC | 55666 |
rs531522644 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605071 | CAAGACCATCCTGAC[C/G]AACATGATGAAATCC | 55666 |
rs531531600 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622572 | CCTTGTTTTGTTTTC[A/G]GACAGTCTCGTTCTG | 55666 |
rs531588943 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622358 | ACACCAGACACTACT[A/G]GAAGAGTATTCACCA | 55666 |
rs531607278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598903 | ATGAAAAACCCAAGG[C/T]GGTGGCAACAGAGAA | 55666 |
rs531613163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560204 | GGGTGGATCACTTGA[A/C]GTCAGGAGTTTGAGA | 55666 |
rs531614199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575120 | TTTCTTTTTTTTTGA[A/G]AGGGAGTCTCGCTCT | 55666 |
rs531627758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581557 | AGTGAGGAGACAACT[A/G]GCTCCAGCCAGAGGG | 55666 |
rs531726310 | in-del | -/GT | 0.00119737 | 0.0244387 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556478 | GCAGGAACACAGGCA[-/GT]GTGTCACCCCCAGGC | 55666 |
rs531729140 | in-del | -/T | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635687 | CTGGGATTACAGGTG[-/T]TGAGTCACCGCGCCG | 55666 |
rs531730683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570018 | GTTCCTTTGGGACTA[C/T]TTCTAAAGAATGAGT | 55666 |
rs531736043 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616798 | ATAATTAACAGAGAG[C/T]TAGACTGCCAAAGAC | 55666 |
rs531764036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609052 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 55666 |
rs531766341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592551 | TTCCAGAGGTGAAAA[A/G]AGCCCAAGGATGATC | 55666 |
rs531777329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565035 | TGGTGACTGAGGGTC[C/T]GGAAGACACGCAATG | 55666 |
rs531805686 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592034 | TCATTGGGGCTCTTA[C/T]ACTCTGAAGCCTCAT | 55666 |
rs531834781 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636463 | CTCTCCTTAGTGACT[C/G]ATGACAAGGCACTTG | 55666 |
rs531848693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592993 | CTCAAAAAAAATTAA[A/G]AATAAAAATAAAAGA | 55666 |
rs531853992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609866 | AGATGTGAGATTCAA[A/G]GCAAAGTAAATCAAC | 55666 |
rs531896341 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630435 | GGAACCACAGGCTTG[C/T]ACCACCACACCAGGT | 55666 |
rs531934638 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635069 | TTTAAAGGCCAGGCG[C/T]GGTGGCTTATGCCTG | 55666 |
rs531970421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597627 | CTGTCTCTACTAAAA[A/C]TACAAAATTAGTTGG | 55666 |
rs532011851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625634 | AACTCGGAAGGCTGA[A/G]GTGGAAGCACTGCTT | 55666 |
rs532056584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629559 | TCAGCTGTGACAAAC[A/G]TCTCATCCTATAGCA | 55666 |
rs532085945 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624320 | CTACTCAGGAGGCTG[C/T]GGCAAGAGAATTGCT | 55666 |
rs532094306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629053 | CCGGCTAATTTTTTG[G/T]ATTTTTACTAGAGAT | 55666 |
rs532097872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563441 | TGGGTGTAGTGGCTC[A/G]TGTTTATACTCCTAG | 55666 |
rs532108235 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586346 | ACTTTGGGTGGCCTC[A/C]CGCCTATAATCCCAA | 55666 |
rs532122700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596811 | ATCAAGAAGAACTTC[C/T]TGAAAAATAATGGGG | 55666 |
rs532171448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602206 | GATCTCGCTCAGGAG[C/T]GAGACCTTGTTTCAA | 55666 |
rs532207683 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591138 | CTGGTTAGGACACCA[A/T]GAAAACCTGGACTGG | 55666 |
rs532211482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597141 | AAATAAATAATGGGG[A/C]CTGAAAGCTAGAACC | 55666 |
rs532234048 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568773 | CATTTGGGAAAATTA[A/C]GAGGTCCACTGAAGA | 55666 |
rs532270770 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589242 | AGTTAAAAAATGTTC[A/G]GTAGTCGGCCGGGTG | 55666 |
rs532348794 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591873 | GTTTTTTAACCAGAT[C/G]CCCAGCAAGTAATTT | 55666 |
rs532377659 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624579 | CTCTAGCCTGGGCAA[C/T]GGAACAAGACTCCAC | 55666 |
rs532394746 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584301 | TTCTAGCCTATTCTC[A/G]CTAACAGAGGGCAAA | 55666 |
rs532411780 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614728 | GGCATGGCAAACTGC[C/T]GACCTCAGAGGCTAA | 55666 |
rs532439932 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619410 | CAAAATTAGCCGGGC[A/G]TGGTGGCACATGCCT | 55666 |
rs532455881 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618359 | CCGCGACCCCGTCTG[A/G]GAGGTGAGGAGCGTC | 55666 |
rs532467316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581120 | TCTGGGAGGCCAAGG[C/T]GGGTGGATGACCTGA | 55666 |
rs532493397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617870 | TTCGCTGTGTTGGCC[A/G]GGCTGGTCTCCAGCT | 55666 |
rs532496244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628286 | GGCTCACACTGAAGC[A/G]GGTGGATCACGAGGT | 55666 |
rs532509354 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627389 | GAAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55666 |
rs532524646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578563 | TGGCTGGGGAGCCCT[C/G]AGGAAACTTACAAGC | 55666 |
rs532524937 | in-del | -/AAAGAACGAAAACCTGG | 0.245631 | 0.249962 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576634 | CTTTGTATAAAAGAC[-/AAAGAACGAAAACCTGG]CGTGTGTTTGCAACA | 55666 |
rs532596833 | in-del | -/TCAGGAGGCTGAG | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562831 | TGTAGTCCCAGCTGC[-/TCAGGAGGCTGAG]GCGGGAGGATTGTTT | 55666 |
rs532615971 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613613 | GGCCTAAACAATGAG[G/T]TTTCTAACTTTTAAG | 55666 |
rs532647403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601425 | TGCATAAGCAAATTT[C/T]TGTGTGTGTATTTTT | 55666 |
rs532669549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584969 | GAGCTCAGGAGTTCA[C/T]GACCAGCCTGGGCAA | 55666 |
rs532671133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562975 | AAAAAAAGGTCAGGT[A/G]CAGTGGCTCACAGCT | 55666 |
rs532753277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579485 | CCCCCTTCACAAGTT[C/T]CTGGTCTAAAAGGTG | 55666 |
rs532833242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568914 | GTCACAAGAATGAAT[C/T]GGGAGCATTTGAAAG | 55666 |
rs532854038 | snp | C/T | 0.213333 | 0.247296 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563177 | GCTTCCTGGGTCAAG[C/T]GATTCTCCTGCCTCA | 55666 |
rs532875115 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558852 | GAGCTCCCAGCCAGA[A/G]AAACATGGGGGCAGG | 55666 |
rs532897145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568350 | CAATAACTGGCTTTG[C/T]ACCTCTGTGAGCACC | 55666 |
rs532903926 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572691 | CTCCACCCATGGCGC[A/T]TGGCCTGGCACTCAG | 55666 |
rs532939067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594844 | CCAACTACATAGGAG[A/G]CTGTTGGGGTCGGAT | 55666 |
rs532946913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561787 | GTTTTTTTGTACAGA[C/T]GGGGCTTCACTATGC | 55666 |
rs532953387 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634812 | CCAGTCTTGAACTCC[C/T]GACCTCGTGATCCGC | 55666 |
rs532992137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611745 | GCGGGTGGATCACAA[C/G]TCAGGAGATAGAGAC | 55666 |
rs533019879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599977 | GGGAGAGCTCAGGCA[A/G]AAGGGACACACATGC | 55666 |
rs533038308 | in-del | -/A | 0.273318 | 0.24891 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597783 | ATGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 55666 |
rs533069249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612315 | GCCTCTGTGCTTCCT[A/G]ATAGGCAGGATCTAA | 55666 |
rs533125888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637737 | TCAGGAGTTCAAGAC[C/G]AGCCTGACCAACGTG | 55666 |
rs533128201 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600582 | AAAACACATGCGACA[C/T]GCCTCCCGGCTTCTC | 55666 |
rs533200585 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630488 | GGAGTGTCATATTTC[C/G]CAGGCTGATCTCGAG | 55666 |
rs533204962 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605053 | ATCATGAGGTCAGGA[A/G]ATCAAGACCATCCTG | 55666 |
rs533239419 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81556974 | GCACACCTGTGAGCC[A/G/T]AAACAGAGCCGAAGC | 55666 |
rs533248722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632666 | TCTGTGAGGTTACCA[A/C]GAGTGTTACATTAAA | 55666 |
rs533259938 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620658 | TGAGGTGTTCAGTAC[A/G]TATTTTGTTTAATAA | 55666 |
rs533264869 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558331 | CGGTGACCCAGCTCT[C/G]CCACCCAGGCCATCG | 55666 |
rs533322552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626968 | GGTGGTGCGAGCCTG[C/T]AGTCCCAGCTACTCG | 55666 |
rs533390869 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630256 | TCAAGAGTCCTACAA[A/T]TTAAAAGAATCACAG | 55666 |
rs533407237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598512 | GAGAAAGGCACATAA[A/T]ACAAAAGGGGTAATA | 55666 |
rs533425259 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620995 | ACCACCGCACTCCAG[-/C]CTGGGTGACACGGTG | 55666 |
rs533431892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599176 | TGCCTGTAATCCCAG[C/T]TACTTGGGAGGCTGA | 55666 |
rs533469699 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574021 | ACAGGGCCTACTGCA[C/T]GGGGTCCTGGGGCCC | 55666 |
rs533485724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583020 | TGAGCGCCCATGTGC[A/G]CCAGCACAGCAGCCA | 55666 |
rs533506537 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619684 | AAGAGATTGAGATCA[C/G]CCTGGCCAACACGGT | 55666 |
rs533506645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614483 | GCCAGCTTCTGCCAT[C/T]ATCACCACCCCCCAA | 55666 |
rs533526313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621473 | GCAACCTGCAGCGTC[A/G]AGAGGAAAACTGGCC | 55666 |
rs533557039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586085 | AGATCAGGAGTTCGA[C/G]ACCAGCCTGCCCAAC | 55666 |
rs533560867 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598353 | AGCACCATGCTGGGT[A/G]CAAGAGACACAGCAG | 55666 |
rs533568968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594149 | GCATGGTAGCGGGCA[A/C]CTGTAGTCCCAGCTA | 55666 |
rs533604601 | in-del | -/AG | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570940 | AACTTCCTTTATAAA[-/AG]AAGAGGAAAGAAGTG | 55666 |
rs533619217 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602857 | CAAGCCTGGGTAACA[G/T]GGCGAGATCTGTCTC | 55666 |
rs533652086 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616811 | AGTTAGACTGCCAAA[A/G]ACTCAGACACAGAAA | 55666 |
rs533704150 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595597 | TCACCCAGGCTGGAG[C/T]GCACTGGCACAAACT | 55666 |
rs533707750 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636016 | CTCGCTCTATAGCCC[A/G]GGCTGGAGTGCCATG | 55666 |
rs533751893 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605197 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGT | 55666 |
rs533758007 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574880 | ACAAACAAACAAACA[A/C]ACACACACACACACA | 55666 |
rs533759820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581271 | GCAGGATTGCTTGAA[C/T]CTGGGAGGCGGAGGT | 55666 |
rs533771944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580545 | GGCCACCCTGCTTAT[C/T]ACTCTCTGTGTGGGG | 55666 |
rs533795197 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609927 | CTTTGTGTCAGATCG[C/G]AAAAGGATTGTCCAG | 55666 |
rs533817917 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621910 | CACGCCGTACATGGA[A/C]AAAGACAATAACTTT | 55666 |
rs533865225 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636564 | GGGGCAGGACTGGCT[A/G]GGAGTCCCTGGAATT | 55666 |
rs533901661 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575192 | GCAAGCTCCGCCTCC[A/C/T]GGGTTCAAGCCATTC | 55666 |
rs533955376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574074 | GAGATTTGGTAGGAG[A/G]CAAAAATCAAATCCA | 55666 |
rs533984665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596515 | AAGCTGTAGTGAGCC[A/G]AGATTGTGCCATTGC | 55666 |
rs534004583 | snp | A/C | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569573 | GGAGGGCAAATGAGC[A/C]ATCAGCCAGCTTTCA | 55666 |
rs534019803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603095 | GATTGCTTGAGCCCA[A/G]GAGGGCTGCAATTGA | 55666 |
rs534020761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563593 | AAACAAAAAAGAAAA[A/G]AAAAAAAAAGACTGG | 55666 |
rs534031973 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597853 | GTAATTCCAACACTT[C/T]GGGAGGCCAAGACGG | 55666 |
rs534043243 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601750 | ATGGCAAAGGCCTCA[A/T]GAAACACTACATCTA | 55666 |
rs534095954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597440 | AGAATCACGAGGTTA[A/C]GAGATCGAGACCATC | 55666 |
rs534139005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628707 | AAATAAGGAAGAAAC[C/T]GTGAAGATAAGCTAA | 55666 |
rs534139492 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561220 | CCTCGGCCTCCCAAA[C/G/T]TGCTGGGATTACAGG | 55666 |
rs534140298 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558502 | CACTCATCACCCTGG[A/G]CACAACCTCGGGGGC | 55666 |
rs534157980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568540 | ACACAGTATGCAGGC[A/G]TGACAGCAAATCGGA | 55666 |
rs534163219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597017 | TCTCCTGAGGCTGAG[C/G]CAGGAGAATGGCGTG | 55666 |
rs534183396 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619604 | AGGCGGGGTGCCAGG[C/T]GCAGTGGCTTACATC | 55666 |
rs534209020 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627756 | CTGGGCAACAAGAGC[A/G]AAACTCTGTCTCAAA | 55666 |
rs534261544 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558860 | AGCCAGAAAAACATG[A/G]GGGCAGGGAGGCCAA | 55666 |
rs534268652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592396 | CAGTCGGCCACCACC[A/C]TCGGGAAAGGGAGAC | 55666 |
rs534284235 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558098 | TAAGAGCCATGCCCC[A/G]GCCTGGCCACGCCAC | 55666 |
rs534292754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627691 | GAGAATTGCTTGAAC[A/G]CAGGAGGCAGAGGCT | 55666 |
rs534301245 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589510 | GCCGCTGCACTCCAG[C/G]CTGGGTGACAGACTC | 55666 |
rs534328330 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633836 | CAAGCCTCCCAAGTA[A/G]CTGGGATTATAGGCG | 55666 |
rs534354141 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558963 | AGGTGCCACGTAGAG[A/G]CGAGAGGTCTTTCCA | 55666 |
rs534374449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629326 | CTTCCCAAGTAGCTG[A/G]GATTACAGGCACCTA | 55666 |
rs534381711 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583907 | AATTGGTATTATACT[C/G]TAGGTATAGATGCAT | 55666 |
rs534409934 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636616 | CCGGGAAACGGGTGG[A/G]GAAGGAGGGCGGTTT | 55666 |
rs534447734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638028 | GTATACATATTTCAC[A/T]ACATCACAATTACTG | 55666 |
rs534500240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578974 | TGCCCAGGCAGGAGT[A/G]TAGTGGTGCAATCAA | 55666 |
rs534512219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584605 | TGGGAAAAGCCCAGA[A/G]AATGAGAAGGGCTGA | 55666 |
rs534553025 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559860 | GCCTCAGCCTCCCAA[C/G]TAGCTGGGATTACAG | 55666 |
rs534580605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634132 | CTGCCTCGGCCTTCC[A/G]AAGTGCTAGGATTAC | 55666 |
rs534581192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595365 | CTTGAACCCAGGAGG[A/C]GGACGTTGCAGTGAG | 55666 |
rs534598475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607318 | AAAAACTACTGTTGA[A/G]GACTGTCAATGAGAA | 55666 |
rs534613392 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573932 | GTGTCCTCCTTCCAC[A/G]TGACGAGTGGCTGCC | 55666 |
rs534634722 | snp | A/G | 9.93904e-05 | 0.00704878 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613392 | CTCATCCTCCACCAC[A/G]TTGGGAGCGCCAAAG | 55666 |
rs534638275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573646 | TTCTGGCCTGAAATG[C/T]GTCTCAGTTCTCCAT | 55666 |
rs534646101 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631811 | TAGCTCATTTTTTTT[C/T]TCCCCGAGATGAAGT | 55666 |
rs534744801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622862 | GGCCAATGGCTATGT[C/T]TGAAAAGTTCAATTT | 55666 |
rs534747564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628040 | ACATGGTGAAATCCC[A/G]TCTCTACTAAAAATA | 55666 |
rs534771553 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618070 | CTGCAGCCTCTGCCC[A/G]GCCGCCACCCCGTCT | 55666 |
rs534791820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611953 | TGACAGAGCGAGAGT[A/C]CATCTCAAAAAAAAA | 55666 |
rs534829490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599737 | GGGAACTGTATCAAT[A/G]TCAGATAAACCAGAT | 55666 |
rs534870416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638830 | TGATCTGTTTTTTAA[C/T]AGTGATGTTATCCTG | 55666 |
rs534901399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613802 | TGCTGGGTTTCAGGG[C/T]CTCTCCTCCCGCCTC | 55666 |
rs534928996 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572338 | GGACTACAGGCGCCC[A/G]CCACCACGCCCGGCT | 55666 |
rs534940402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618445 | CGTCTGGGAAGTGAG[A/G]AGCGTCTCCGCCTGG | 55666 |
rs534974694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616574 | TCTCTACTAAAAATA[G/T]AAAAAATTAGCCGGG | 55666 |
rs535012938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583176 | ATATCTATCAAAACT[C/T]GAAAAACCTTCCTCC | 55666 |
rs535025349 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582923 | CCAGCCTCCCGATTC[A/C/G]AAGAAACACACAAAA | 55666 |
rs535031937 | in-del | -/A | 0.495407 | 0.0477027 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626318 | AGACTCCATCTCAAG[-/A]AAAAAAAAAAAAGAA | 55666 |
rs535034192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561173 | CATGTTGGCCTGGCT[C/G]TCTCGAACTCCTGAC | 55666 |
rs535038829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586468 | CACAAAAAATTAGCC[A/G]GGCAGGTGGCACACA | 55666 |
rs535069114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571213 | ATCACGTGCCCATCC[A/G]ATTTCAAATGCAGCC | 55666 |
rs535115786 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611409 | GGCTGGAGTGCAGAG[A/G]TATGATCTCGGCTCC | 55666 |
rs535134500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598673 | TGTGTGATCCTTAGG[C/T]CCGCCTCTGCCTGTG | 55666 |
rs535183808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604859 | ATAGGGTGTGATGGT[A/G]CATGCCTGTGGTCCC | 55666 |
rs535187346 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585156 | GCCTGGGCGACAGAA[A/C]GAGACTCTGTCGCCA | 55666 |
rs535207378 | in-del | -/GATC | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616271 | CTTGCAGTGAGCTGA[-/GATC]GATCGCACCACTGCA | 55666 |
rs535267981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612463 | GGAAGAGGCATGCCG[C/G]CTAATGGCTATGGCT | 55666 |
rs535290414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600210 | AAAACATATAGTGCC[C/T]GCACCTGACCTTGTG | 55666 |
rs535298193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637835 | GCTACTCGGGAGTCT[A/G]AGGCCGGAGAATCTC | 55666 |
rs535332380 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600577 | CAGATAAAACACATG[C/T]GACACGCCTCCCGGC | 55666 |
rs535340434 | in-del | -/AAAAAAAA | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614289 | AAAAAAAAAAAAAAA[-/AAAAAAAA]GTGGGATTACCAGAG | 55666 |
rs535355490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599726 | AAATTGTTCCTGGGA[A/T]CTGTATCAATGTCAG | 55666 |
rs535362188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627085 | ACACAATGAGACTTC[A/G]TCTCAAAAAAAAAAA | 55666 |
rs535375722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567036 | GGAGGGGAGATATGA[C/G]TAAAAAGCAGAGGCT | 55666 |
rs535388685 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557211 | TCCCACAAGAGGAGG[C/T]GGCTGAGCCTCCCAG | 55666 |
rs535424365 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559166 | TCCAGGGCTGCCCAC[C/T]ATGGGGCAGTTACAG | 55666 |
rs535450584 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592173 | GGCGCCCCGCACCCT[A/G]TGCCACATGGCTCAG | 55666 |
rs535528554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559877 | AGCTGGGATTACAGG[A/C]ATGAACCACAATGCC | 55666 |
rs535546556 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592655 | ATTCTAAAAATGTGC[C/T]AGTTCTTCTGGCCCA | 55666 |
rs535559042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559484 | GCCAGAGTGTGGGCA[C/T]GGGGGCAGGGGCAGG | 55666 |
rs535582246 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637329 | GCATCCGAAGTCTCA[A/C]CCAAAAATAACTACT | 55666 |
rs535594256 | snp | C/T | 0.000150818 | 0.00868253 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565336 | CACCGGAGCCTGCCA[C/T]GTGCCTGGCAGGGAG | 55666 |
rs535606056 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597919 | CTAACATGGTGAAAT[C/T]CCGTCTCTACTAAAA | 55666 |
rs535616875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560266 | CTACTAAAAATAATT[A/C]GCCAGGCGTGGTGGT | 55666 |
rs535618182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578460 | TCTCAACAGATAAAC[A/G]GTACGACTGGTCCGT | 55666 |
rs535662624 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586751 | AATGAGACAAAGATT[G/T]AAGGAAGACTGTCAC | 55666 |
rs535757826 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616173 | AATAAAAAAAAAAAT[G/T]AGCCGGGGGTGGTGG | 55666 |
rs535771342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577991 | CCTGCCCACCCCATC[C/T]GGCTGTCAGCACCTG | 55666 |
rs535816628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629958 | CAGCTCAATCCTTCT[A/G]GAATATGATGCCGAG | 55666 |
rs535824935 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592152 | GACCTGAGTGCTGTC[A/G]GCAGGGGCGCCCCGC | 55666 |
rs535830589 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618519 | CCCGGCCAGCCGCCC[C/T]GTCCGGGAGGGAGGT | 55666 |
rs535851946 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635940 | TTTCTGATTTGTCAC[C/T]GATATTTTTTACGTT | 55666 |
rs535870299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579942 | CGGCAGCCGCTTATC[C/T]ACTACTCAGCCAGGC | 55666 |
rs535877873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591193 | TAATTCCAGCACTTT[A/G]GGAGGCCGAGGCAGG | 55666 |
rs535888274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597401 | CACGCCTATAATCAC[A/G]GCACTTTGAGAGGCC | 55666 |
rs535957489 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564609 | CCTGGCTAACATGGT[A/G]AAACCCTGGCTCTAC | 55666 |
rs535965218 | in-del | -/AAAC | 0.00637571 | 0.0560999 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602234 | AAAACAAAACAAAAC[-/AAAC]AAACAAACAAACAAA | 55666 |
rs535975605 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594364 | TATTAACATAATTAA[C/T]GTGTGAAAGATGCCT | 55666 |
rs535990754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624904 | ACAATAAGGAAGATG[A/G]AAAGAGATGAGGCTG | 55666 |
rs536016251 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620500 | GACTCCGTCTCAAAA[A/T]AAATAAATAAATAAA | 55666 |
rs536017479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575163 | GGAGTGCAGTGGCGC[A/G]GTCTCGGCTCACTGC | 55666 |
rs536098409 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614848 | GGAAGAAAGGCTGCA[C/G]CATGTCCTCTGACAG | 55666 |
rs536125733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564449 | TCGGCAATAGAGTGA[A/G]ACCCTGTCTCTACAA | 55666 |
rs536162981 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622599 | TCTGTAGCCCAAGCT[A/G]GAGTACAGTGGCATG | 55666 |
rs536169022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615649 | TCACTCACAGCTTTG[G/T]GCCTACAGCGGTTTG | 55666 |
rs536176468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620853 | GATTTAAACTTTTTT[A/T]TAAAAAATTACCAGC | 55666 |
rs536198999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569534 | AGCTGACTTTGCTCA[A/G]GAGAGATTCGTGTCA | 55666 |
rs536208937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560271 | AAAAATAATTAGCCA[A/G]GCGTGGTGGTAGACA | 55666 |
rs536235943 | snp | C/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562162 | ACTTGAACCCAGGAC[C/G]TGGAGGTTGCAGTAA | 55666 |
rs536248068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585665 | GACTCCATTTCTGGG[C/G]GGGGGGGGAAAGAAA | 55666 |
rs536328637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614387 | TAATTGCTATGACAA[C/T]GGCTGCCTCAATTCC | 55666 |
rs536367948 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619079 | TGCGGAAGGCCGCAG[C/G]GTCCTCTGCCTAGGA | 55666 |
rs536413828 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558567 | TCTCTCACTCCCCTT[C/T]TGTGCAGTTTTTATC | 55666 |
rs536493009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595569 | TCTTTTTTTGAGACA[C/G]AGGCTCACCCTGTCA | 55666 |
rs536494580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608595 | ATAAATATAGAACCA[C/T]GGTAACTTTCAAAGG | 55666 |
rs536557388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609211 | TTTTAGTGGAGACGG[A/G]GTTTCAGCATATTGG | 55666 |
rs536562099 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567028 | ATTTAGGAGGAGGGG[-/A]GATATGAGTAAAAAG | 55666 |
rs536605970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573553 | TTACAGATCCAACTC[C/T]TTGTTCTACTCTCTC | 55666 |
rs536612598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561141 | TTTTTTTATTTTTAG[C/T]AGAGATGGGTTTTCA | 55666 |
rs536626402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594478 | AGACTTCATTTCTAC[C/T]AAAAATTTAAAAATT | 55666 |
rs536658536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638722 | GTGCTGAGTCGGTTC[C/T]TGGGTGGGGGCCACA | 55666 |
rs536665351 | snp | C/T | | | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596193 | TTGGGATGCTTGTTC[C/T]GGAAGTCTCCTGCAG | 55666 |
rs536726612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568386 | TCCCCTGGGCGGATG[A/G]GCACTGAGGGGATCA | 55666 |
rs536726961 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562479 | GGGAGGTGGAGGCTG[C/T]AGTGAGCTGAGATCA | 55666 |
rs536800232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622685 | CCTCCCAAGTAGCTG[A/G]GATTACAGGCGCCTG | 55666 |
rs536807951 | in-del | -/G | 0.000370062 | 0.0135976 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565624 | TACAAGAAGCCAAAA[-/G]GAAGGTTCCTCTTCG | 55666 |
rs536827567 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634815 | GTCTTGAACTCCTGA[C/T]CTCGTGATCCGCCCA | 55666 |
rs536858763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589463 | GAATGGCGTGAACCC[A/G]GGAGGTGGAGCTTGC | 55666 |
rs536921311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590789 | GAAAGCAAACCTGAC[A/G]GCCACACAATCAAAA | 55666 |
rs536958077 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558834 | AGACAAGGGGGTAAC[A/C]AAGAGCTCCCAGCCA | 55666 |
rs536963280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617618 | ATCGAGACCATCCTG[A/G]CTAACACGGTGAGAT | 55666 |
rs537016659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633114 | GCCTGGGTGACAGAG[C/G]AAGACTCCGTCTCAA | 55666 |
rs537035428 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600032 | CTGGGGTCTGTTTCC[C/G]ACTTGAAGCAGTCCT | 55666 |
rs537072831 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626085 | ACCTGGGAGGTGGAG[A/G]TTGCAGTGGGCAGAG | 55666 |
rs537108529 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607941 | TCGTTGCACTGACAG[G/T]AATTATAAAATAATA | 55666 |
rs537129612 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616532 | TCAGGAGATTGAGAC[A/G]ATCCTGGCTAACACG | 55666 |
rs537177582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627260 | AGCCGGGCATGGTGG[C/T]GGGTGCCTGTAGTCC | 55666 |
rs537206732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571828 | TTAAAACTGTGAGCA[C/T]TTCAGCAACACCGCA | 55666 |
rs537214567 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589626 | GACACCCTGCAGCTC[C/T]GCACACACTTGGCTC | 55666 |
rs537267848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576810 | GTGGTCAAAGAAGCA[C/G]AGAGAGCGGGGTCCT | 55666 |
rs537330818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617939 | GCCGGGATTGCAGAC[A/G]GAGTCTCGTTCACTC | 55666 |
rs537331552 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566302 | GCGCCAATGCACTCC[A/G]GTCTGGGCAACAGAG | 55666 |
rs537392928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566021 | TCTATCCTAGCCTTC[C/T]GAGTCAAACTGCAGG | 55666 |
rs537393322 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572200 | TTTATTTATTTATTT[A/T]TTTTTTGAGACAGAG | 55666 |
rs537422548 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633759 | CCCAGAGTGGGAGTG[C/T]GATGGCGCGACCTCG | 55666 |
rs537430931 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558396 | CTGCTCAGCCCGCAG[C/T]ATCTGCAGTTGCTGC | 55666 |
rs537432324 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617689 | CTCCGTCTCTTTCCA[C/T]GGTCTCCCTCTCATG | 55666 |
rs537434615 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575547 | ACACACTGGTCACAG[A/G]CACTACTGCTGTCCA | 55666 |
rs537454156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593786 | CTTTGTTCTCTGCTC[A/C]CCTCCTGGGTGCCCA | 55666 |
rs537486592 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615611 | TCAGAGCTGCTTGTG[G/T]GGCCAAGGCCACTCT | 55666 |
rs537533625 | in-del | -/AAAA/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591447 | TCTGGAGTAAAACAG[-/AAAA/C]AAAAAAAAAAAAAAA | 55666 |
rs537550342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609975 | CTGCCCCTTTATCAC[A/G]GCCACACAAATGCTT | 55666 |
rs537605448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559516 | AGCTGAGAGCTCCCC[A/G]CCCCCAACATCCCAC | 55666 |
rs537605933 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637239 | GGGATTTTGGAAAGT[C/T]GCGTCTGAGATTACT | 55666 |
rs537618217 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567317 | CTTTGACCCAGTTTC[C/T]CAATCATGCTCTGGT | 55666 |
rs537682437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611609 | CCTGCCTCAGCCTCC[C/G]AAAGTGCTGGGATTA | 55666 |
rs537692956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616853 | AATATCAACCTCTAC[A/G]TGGGATATTAAATGA | 55666 |
rs537738802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626031 | GTGCACCCCTGTAAT[A/C]CCAGCTACTCAGGAG | 55666 |
rs537744329 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611829 | GCCAGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 55666 |
rs537744354 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608387 | GCAGCCAGGCGCCTG[-/CA]CAGTCGCTCTGCCTT | 55666 |
rs537744367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605257 | CTGCACTCCAGCCTG[A/G]GCGACAGAGCAAAAC | 55666 |
rs537814069 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574509 | TTAGAAAATGTCAGT[C/T]GGAATGCGCTGGGAG | 55666 |
rs537864899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569213 | CCAAATTAACGACTC[C/T]TAGCAATTCTGAGAA | 55666 |
rs537868399 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575248 | GGGACTACAGGTGCC[C/T]GCCACCACGCCCGGC | 55666 |
rs537872519 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619442 | TAATCCCAGCTACTC[C/G]GGAGGCTAAGGCAGG | 55666 |
rs537936874 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559128 | GTGGGTCAGGGAGCC[C/T]AGGACAGCCAGCCCC | 55666 |
rs537969908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570288 | TCCTCAGGATGAAGA[A/T]GATCGGAGTACTCGC | 55666 |
rs537981975 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557437 | GGAAATGCTGGTGGA[A/G]GACAACGGAAACTAT | 55666 |
rs537994238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565184 | GGCGCTTCCATAAAG[C/T]TTCTGATTCTCTTAA | 55666 |
rs537995566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564413 | TGCAGTGAGTTACGA[C/T]TGTGCAACTGCACTC | 55666 |
rs538036646 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558323 | ATCGGCACCGGTGAC[C/G]CAGCTCTCCCACCCA | 55666 |
rs538046027 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636702 | GGGCGGGGAACCGGG[A/G]TCGTAAGTCCCCTGG | 55666 |
rs538047513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586168 | AGACCCCCAGCAAAG[C/G]GGACTGTGGCACTGA | 55666 |
rs538055139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571148 | GTGCATCGATGGGCT[C/T]GGCTCGTGGGGACCT | 55666 |
rs538060008 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592100 | GGGAGGAAGGACAGA[A/C/T]GCAGAGGGAGAGGCG | 55666 |
rs538113685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586659 | GGTACATGGGATACC[C/T]ACATATTTAAGCTGT | 55666 |
rs538129796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615192 | GGAACCTGCATCTCA[C/T]GGGTTTAAGCGATTC | 55666 |
rs538143384 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638542 | ACCTCAGGTGATCCG[-/C]CCACCTGGGCCTCCC | 55666 |
rs538167552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560400 | CCTGGGCGACACAGC[A/G]AGACTCCATCTCAAA | 55666 |
rs538194291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563784 | TTGCAGCCATAAAAA[G/T]GAATGAAATCATGTC | 55666 |
rs538286830 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602491 | GGGTGGATCACGAGG[G/T]CAGGAGTTTGAGACC | 55666 |
rs538325498 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558310 | GGAGGGCCAGAGCAT[C/T]GGCACCGGTGACCCA | 55666 |
rs538369109 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635842 | ATATTAACCAAAATG[C/G]TCCTGTCCAATGGTC | 55666 |
rs538386866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624797 | AAGCCCGCCACACGC[A/G]AGCTGGGAGAAAAGG | 55666 |
rs538437319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574156 | AAACCTGCAACAACT[C/T]ACACATAATTAGCCC | 55666 |
rs538496912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618904 | TGATCTATGACCTTA[C/T]CCCAACCCTGTGCTC | 55666 |
rs538548192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619777 | CCAGCTACTCAGGAG[A/G]CTGAGGCAGGAGAAT | 55666 |
rs538558725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608131 | CTACTGTGGTACCAT[A/G]AGGATTAGTGGCTGC | 55666 |
rs538564321 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581297 | GAGGTTGTAGTGAGC[C/G/T]GAGATTGGGCCACTG | 55666 |
rs538577992 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568591 | AGAGCAGAGGCCAAC[A/G]CGGGAGCCACGCTAA | 55666 |
rs538669670 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638444 | GCTGGGACTACAGGC[A/G]CACACTACCATGCCT | 55666 |
rs538677253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590121 | CTGTCTTCCAGAAAC[C/T]TACACGGCCGCCACA | 55666 |
rs538684491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612060 | AAATAATCCAAGTTT[A/G]GAAAATACCTACTTC | 55666 |
rs538686441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617533 | TACAAAATTAGGCCG[C/G]GCACAGTGGCTCATG | 55666 |
rs538733440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613266 | ATATTTCCCTTTATT[C/T]ACCCATTAAGATCAC | 55666 |
rs538741021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623833 | ATTCCAATTCTGAAA[C/T]CTAACACAGAATGGT | 55666 |
rs538747863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612588 | ACCGCAAAGTCAGCA[C/G]CCCGTCACATCTACA | 55666 |
rs538824329 | in-del | -/T | 0.334722 | 0.235207 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637456 | ACACCTTCATGTTTT[-/T]TTTTTTAAGTATTTT | 55666 |
rs538831186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579834 | TCCCTGGCAGTGAAA[C/T]CCCCCGAAAGAGTCA | 55666 |
rs538875641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567190 | GTGCAGACACTCAAT[A/G]GAAATGCTAAAGGTG | 55666 |
rs538880481 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626510 | GAGGTCAACGAAGAC[A/G]AGAAGACCAAGAAGA | 55666 |
rs538884096 | in-del | -/A | 0.168135 | 0.236216 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628224 | CATAAAAAAAAAAAG[-/A]AAAAAAAAAAGAAAA | 55666 |
rs538899467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608528 | CCAGCCTGGGCAACA[C/T]AGTGAGACCCCATCT | 55666 |
rs538914141 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600246 | GGAGAGAGCCAGTAC[C/G]CGACACAGCCCGGCC | 55666 |
rs538931671 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558490 | TGCCCCCGTCCACAC[A/T]CATCACCCTGGACAC | 55666 |
rs538935227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614213 | ACCCAGGAGGCGGAG[A/G]TTACAGTGAGCCAAG | 55666 |
rs538939940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634766 | AATTTTTTATTTTTA[C/G]TAGAGACAGGGTTTC | 55666 |
rs538957307 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628084 | AGGCATGGTGGTGGG[C/G/T]GCCTGTAGTCCAGCT | 55666 |
rs539024197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583808 | AGGAAGCTTCTACTC[C/G]CACCCCATGTGTGAG | 55666 |
rs539029178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577863 | CCCCAAGGCCACAGG[A/G]AACTGACATGTGGCC | 55666 |
rs539039620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577512 | TTCCGGGTTAGCTCA[A/G]CGCACTCTTCTCTTC | 55666 |
rs539056694 | snp | A/C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618524 | CCAGCCGCCCCGTCC[A/C/G]GGAGGGAGGTGAGGG | 55666 |
rs539060252 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571758 | TAGTATGGGGACAGT[G/T]AACCCCTAGGTTGAC | 55666 |
rs539110635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605220 | CGGGAGGTGGAGCTC[A/G]CAGTGAGCTGAGATG | 55666 |
rs539160678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599031 | CGGTGGCTCACGCCC[A/G]TAATCCCAGAACTTT | 55666 |
rs539166219 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573095 | GAGCTCCAGAAATAA[A/T]TTCATAAGAACCAAA | 55666 |
rs539233050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588806 | CCAGAAACGTGACAG[A/C]AGCCTTTAGTGACAA | 55666 |
rs539248263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573443 | ATGAGAAGCCCCAGG[A/C]CCCCATTTGGCCCTT | 55666 |
rs539262900 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603510 | CTGAGGCAGGAGGAT[C/T]GCTTGAGCCCAGGAG | 55666 |
rs539331006 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600802 | AAGTAGCTTCACTCC[A/C]AACAGGTTTGGCTAA | 55666 |
rs539395509 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606896 | ATGCTAAGTATCTTA[C/T]ACCTCCTGAACAGTG | 55666 |
rs539432655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565389 | TGCCGATGGCACCTG[C/G]CAGGATGCAGCTGGG | 55666 |
rs539439769 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628101 | CCTGTAGTCCAGCTA[C/T]TCGGGAGGCTGAGGC | 55666 |
rs539476666 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611721 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGCGGGTG | 55666 |
rs539517113 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587391 | CACAATCTTGGCTCA[C/T]TGCAAGCTCTGCCTC | 55666 |
rs539530227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605707 | CAGTGGCGGGACACG[A/G]GGTTATAGGAGGATG | 55666 |
rs539530638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633002 | AGGCGTGGTGGAGGG[C/T]GCCTGTAGTCCCAGC | 55666 |
rs539547391 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556467 | AGACAGCTCAAGCAG[A/G]AACACAGGCAGTGTG | 55666 |
rs539553002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602627 | GAATCACTTGAACCC[A/G]GAAGGCGGAGGTTGA | 55666 |
rs539558177 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566290 | TAAGCCAAGATTGCG[C/G]CAATGCACTCCGGTC | 55666 |
rs539579363 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589752 | CCTGTAATCTGAGCA[A/C]TCTGAGAGGGCAGGG | 55666 |
rs539618296 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557721 | GCATCCGCAGCAGTC[C/T]GCTTCAACCCAGCTC | 55666 |
rs539620410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619117 | AGACCTTTGTTCACT[C/T]GTTTGGCTGCTGACC | 55666 |
rs539650853 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582303 | CATCCGTACCAGGAG[G/T]TTTTCAGCTATGATG | 55666 |
rs539658613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588336 | TTCTAAAAAAGGTCC[C/T]GAAACATCTCCCACG | 55666 |
rs539683683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589313 | AGACAGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 55666 |
rs539693559 | snp | A/C | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636179 | TTTTGCCATGTTGGC[A/C]AGGATGGTCTCGAAC | 55666 |
rs539696422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622625 | GCATGATCTCGGCTT[A/C]CTGCAACCTCCACAT | 55666 |
rs539731627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611352 | AAATAGTTTTTTTTT[G/T]GTTTTCTTTTTTTCT | 55666 |
rs539736898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627537 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 55666 |
rs539755322 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596362 | CTCTAATTCCAGCAC[-/T]TTTGAGAGGTGGAGG | 55666 |
rs539771201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576696 | ATATACAAAGACCTC[A/T]CAAATGAATGCCAAA | 55666 |
rs539774087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625417 | AGAGCTCTACACCGA[A/G]GGGTCATCAGAGTAG | 55666 |
rs539797756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586816 | CCCCTAAGGGGTTAC[A/G]CTGTAGAAAAAGGGA | 55666 |
rs539881192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592749 | AGGACTTTTTGAGGC[C/T]GAGACAGGCGGATCA | 55666 |
rs539884424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581973 | TGGGACGTGCTGACA[A/G]CAGAGACATGCTTCC | 55666 |
rs539936980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620940 | AGGCTGAAGGATCAC[C/T]TGAGCCCAGAAGGTC | 55666 |
rs539955136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620568 | GCAGTGGCTGCCAAT[A/G]CCTTATCCCCAGACC | 55666 |
rs539963163 | in-del | -/A | 0.00398564 | 0.0444627 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556577 | CATGTACCTGTCCAC[-/A]AAGCAGTGACTGTGG | 55666 |
rs539972262 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559634 | AGGGAGTAACAGGGA[A/G]CCTGTGCTTGCTGGT | 55666 |
rs539981756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569285 | GTGTCATCTCTAAAC[A/G]AACACTTGGAAACTC | 55666 |
rs539999739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616234 | GCTGAGACAGGAGAA[C/T]GGCATGAACCCAGGA | 55666 |
rs540017387 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582775 | CAACAGTCTACGAGT[C/G]TGAGTCTTGTCCCTG | 55666 |
rs540041187 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635347 | CCATCTCAAAAAAAT[A/T]AAATAAGGTTAAAAA | 55666 |
rs540061369 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558929 | GCAGCATCGGCCCCT[C/T]CCTGTGCGCCCCAAT | 55666 |
rs540069271 | snp | A/G | 0.000209974 | 0.0102442 | intron-variant, stop-gained, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563974 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGGAGG | 55666 |
rs540112755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604975 | CTTAAAAAATAAACA[A/T]CTGGGCTGGGCGCAG | 55666 |
rs540147559 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624939 | GGCAGACAGGGCCGT[G/T]GGAAGCCACACAGAC | 55666 |
rs540185840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630064 | AACTTTAATTCCTAA[C/T]CACTATTTATAGAGT | 55666 |
rs540189135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608307 | ACAGGCCACCATCAC[A/G]GATGCTAACTTGCTG | 55666 |
rs540214173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568793 | TCCACTGAAGATGTG[A/G]CCAGTCAGGACGTCA | 55666 |
rs540231222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627868 | TGGAACCCAGGAGGC[A/G]GAGGTTGCACTGAGC | 55666 |
rs540258522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601017 | AATCAACCACCTCCT[C/T]TCATCTGGCACAGGG | 55666 |
rs540317789 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596783 | ATGAGACCAAGAGAT[A/C]CGGCCTTCATTGATC | 55666 |
rs540319600 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602734 | AAAAAATCAAACTTC[A/T]GGAAGTCCAACTAAA | 55666 |
rs540324994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627068 | GCACTCCAGCTTGGG[C/T]GACACAATGAGACTT | 55666 |
rs540350848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563334 | TGCCTCAGCCTCCCA[A/C]AGTGCTGGGATTACA | 55666 |
rs540380281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618287 | CCATCGTCTGAGATG[C/T]GGGGAGCGCCTCTGC | 55666 |
rs540383209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589735 | AAAAGGCTCAGATTA[C/T]GCCTGTAATCTGAGC | 55666 |
rs540389381 | in-del | -/A/G | 0.498206 | 0.0298983 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619553 | AAACTCTGTCTCAAG[-/A/G]AAAAAAAAAAAAAAA | 55666 |
rs540400663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624116 | ATGGTGAAACCCCAT[C/G]TCTCCTAAAAATACA | 55666 |
rs540451452 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585259 | CAGAGTCCAGTAACA[C/T]CCATGATTCCTGGAG | 55666 |
rs540482804 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592222 | AGGAGGGATGTGGGA[A/C/T]GGGAATGCAACAAGT | 55666 |
rs540536664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591844 | AGCTGCTATTGAATC[C/T]GAATGCATTTCTGGT | 55666 |
rs540550977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624564 | GATCACGCCATTACA[C/T]TCTAGCCTGGGCAAC | 55666 |
rs540560715 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618572 | GCCAGCCGCCCCGTC[C/T]GGGAGGGAGGTGGGG | 55666 |
rs540584573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562644 | AACTTACACCAGTCA[G/T]AACTGCCTATTATTA | 55666 |
rs540588291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634423 | CAATGCTGTCAATGA[A/G]AGCCTAGCCTTATAC | 55666 |
rs540594270 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558287 | AGTGGGACGAAGCAG[C/T]GTATTGGGGAGGGCC | 55666 |
rs540644982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562227 | ACAGGGTGAGATTCC[A/G]TCTCAAAACAAAACA | 55666 |
rs540688577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577647 | TCCAGACCTGAGTCC[C/T]GGCAACCGTCTGTCC | 55666 |
rs540749432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628278 | GGCACGGTGGCTCAC[A/G]CTGAAGCGGGTGGAT | 55666 |
rs540779489 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558600 | AAAAAAAAATAAATA[A/G]AAGTCTTCTGGGCAG | 55666 |
rs540810264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579329 | ATTGCAGTGAGCCAA[G/T]ATCGTGCCATTGCAC | 55666 |
rs540829671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606247 | GCGGCAGGAGGAAGG[C/T]GAGGCAGGCTACTCA | 55666 |
rs540888997 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609077 | GAGTGCAGTGGCACA[G/T]TGGCACAGTCTCTGC | 55666 |
rs540892004 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579993 | CCTGAGCTGCTGAAG[A/G]CAAAGCCTCCTCTCC | 55666 |
rs540920906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613930 | CCACTGCTTTCTCGG[C/T]GTTCACATACACACG | 55666 |
rs541000341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622406 | TCATTTACCAAATTC[A/C]TCTTGCTATTTTGCT | 55666 |
rs541029513 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627335 | AGGCAGAGCTTGCAG[C/T]GAGCCGAGATCGCGC | 55666 |
rs541056409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571296 | CTTTGGACAGAGCTC[C/T]GGTGGGGCTGATGCA | 55666 |
rs541064191 | snp | A/G | 5.00346e-05 | 0.00500148 | synonymous-codon, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81588965 | AAACACATCAGGCAC[A/G]TACTGCTCACTGCTA | 55666 |
rs541153132 | snp | A/C/G/T | 0.00028158 | 0.0118627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565629 | GAAGCCAAAAGGAAG[A/C/G/T]TTCCTCTTCGCTGTG | 55666 |
rs541189790 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560471 | CCCAGCACTTTGGGA[A/G]GCTGAGGTGGGCAGA | 55666 |
rs541209447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573163 | TTCTATCTAAATCAT[C/G]ACTTAACATTATATA | 55666 |
rs541211019 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626763 | TGACTTTGCCAGTGC[A/C]CTCCAACCTAGGCAA | 55666 |
rs541239666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560128 | TCTTGGATAAAAACA[A/G]AGAGTGAGGCTGGGT | 55666 |
rs541270763 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583745 | TCTTACTGGCTGCAT[A/G]TGGGACAGGGCAAAG | 55666 |
rs541343148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567669 | TGCCTCTGCAACCAC[G/T]AACAGGGTCCAAGAA | 55666 |
rs541363462 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557459 | GGAAACTATAATAGC[A/G]TGGTGGATAAGGACG | 55666 |
rs541376998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594101 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 55666 |
rs541407479 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626950 | CAAAAATCAGCTGGG[C/T]ATGGTGGTGCGAGCC | 55666 |
rs541410434 | snp | A/C | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614339 | ATTTCAACAACCCCT[A/C]ATAAAATCCTCCAAA | 55666 |
rs541438405 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593419 | AGTCCAGAAGCACTG[A/C]CACACCTAAACGTAT | 55666 |
rs541516054 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592878 | AATCCCAGCTACTTG[G/T]GAGACTGAGGCACAA | 55666 |
rs541522422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605344 | AAATAAAAACAATAA[A/C]CATTACTTAAGAAAA | 55666 |
rs541528407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598766 | CACTTCTGTCCTCGG[A/G]AAGGATCTGCGGCCC | 55666 |
rs541542086 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597963 | AGCCGGGCGTGGTGG[C/G]GGGTGCCTGTAGTCC | 55666 |
rs541559459 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605020 | AATCCCAGCACTTTG[A/G]GAGGCCAAGGCGGGC | 55666 |
rs541576649 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635085 | GGTGGCTTATGCCTG[G/T]AATCCCAGCATTTTG | 55666 |
rs541577217 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562430 | TGTAATTCCAGCTAC[C/T]TAGGAGGCAGAGGCT | 55666 |
rs541594436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626128 | CACTCCAGCCCAAGC[A/G]ACAGAGTGAGACTTC | 55666 |
rs541598537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620698 | GGAGGGAGAAAAAAA[A/G]GCCAAGCAACAGAAG | 55666 |
rs541630404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625567 | CTTATCAGCAGAAGG[A/G]AGAGAGCAGAAGAGT | 55666 |
rs541664506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594542 | AGCACTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 55666 |
rs541699328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587061 | CAGACAGACGGTCCA[C/T]GGAAAACACATTGCA | 55666 |
rs541702791 | snp | A/C | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563463 | TACTCCTAGGTACTC[A/C]GAAAGCTGATGCAGG | 55666 |
rs541756649 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616307 | GCCTGGGCGACATAG[A/C]AAGACTCTGTCTCAA | 55666 |
rs541759226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621094 | ATGCAAAACCCTTCA[A/C]GAAAGAAAGAAAAGG | 55666 |
rs541766235 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586626 | AAAAAAAAAAAAAGA[G/T]GCTTGCAAAAGTTTT | 55666 |
rs541805942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585779 | ATTGCTTGAGCCTAG[G/T]AGTTCAAGACCAGCC | 55666 |
rs541807116 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564933 | GGGACTCAGGGCACT[C/T]GGGCTGCACGAGGCA | 55666 |
rs541863085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585494 | TGGTGAAATCCAATC[C/T]CTACTAAAAATTTAA | 55666 |
rs541869145 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629442 | ATCCACCCGCCTTGG[A/T]CTCCCGAAGTGCTGG | 55666 |
rs541871324 | in-del | -/A | 0.436692 | 0.166271 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589851 | ATAAATCAATCAATC[-/A]AAAAAAAAAAAAAAA | 55666 |
rs541893864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580827 | GTGAGAGCATCGCAC[A/G]GTGAATCAGGTCAGT | 55666 |
rs541927241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592432 | CAAGTCTGAGCACCA[A/C]GAGGGGTGATTCACA | 55666 |
rs541977997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608865 | AGTCTCACACGTGCC[A/G]GTCACTCCAGGCGCT | 55666 |
rs541985126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559638 | AGTAACAGGGAGCCT[A/G]TGCTTGCTGGTTCCT | 55666 |
rs542013616 | in-del | -/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557699 | CGCGGTGGGCAAGCT[-/G]GGAGTTGCATCCGCA | 55666 |
rs542025604 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582161 | GAGAACTTATGATTC[C/T]AGGAGCCCAAGCTGA | 55666 |
rs542100555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603608 | TCTAAAAAATAAATA[A/C]ATAAAAATTAAAAAT | 55666 |
rs542111691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582460 | AGGCTGGAGTACAGT[A/G]GTACAATCATAGCTC | 55666 |
rs542111945 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605630 | TTCAGCCTGGGCTAC[A/G]GAGTGAGACTCTGTC | 55666 |
rs542129184 | in-del | -/AGG | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581035 | TTTCCTCATGGCTGA[-/AGG]AGAAGAAAATAGAGA | 55666 |
rs542143880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616030 | TGTAGAAAAGCTGCT[A/G]AATCTGGGCCGGGCG | 55666 |
rs542175284 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558590 | TTTTTATCTTAAAAA[A/T]AAATAAATAAAAGTC | 55666 |
rs542196308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569826 | CCTAAGATATAATCA[A/G]TAGATGCTACAGGGA | 55666 |
rs542198655 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581142 | ATGACCTGAGGTCAG[A/G]AGTTTGAGACCAGCC | 55666 |
rs542211501 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589822 | GGGCAACATAGTGAG[A/C]CCCTATCTTTACAAT | 55666 |
rs542260706 | in-del | -/GA | 0.0103295 | 0.0711199 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618897 | ATCCTGTTGATCTAT[-/GA]CCTTACCCCAACCCT | 55666 |
rs542304472 | snp | A/T | 0.462691 | 0.131387 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614572 | TCAGACTTAAGGGTT[A/T]CTGCTTGTCTCTGAA | 55666 |
rs542394599 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574252 | CACTTTAATCTCCCC[C/G/T]TCTAGGGATTTTTCT | 55666 |
rs542398358 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592685 | ATGGAATAATTTCTC[C/T]ACAGACACAGTAATT | 55666 |
rs542408439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569364 | TGCACCGGCCTCGAC[A/G]TCGGACAAAAAGGGC | 55666 |
rs542420631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575069 | GCCGCCACAGGATAA[C/T]TCAGAAAAAACAAAG | 55666 |
rs542436787 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562911 | CCACTGCACTTCAGC[A/C]TGGGTGACAGAGTGA | 55666 |
rs542566015 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613557 | CTTCATGGAAGCCCA[A/C]CTTGGATATCTGCAA | 55666 |
rs542603872 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635318 | AACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 55666 |
rs542609248 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559802 | CAGTGGCACGATCTC[A/G]GCTCACTGCAACCTC | 55666 |
rs542619489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579207 | GGCAAAACCCCTCTC[C/T]ACTAAAAATACAAAA | 55666 |
rs542642627 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633644 | CTATTTATAAGAAAA[C/T]AAGACTAGAACGCTT | 55666 |
rs542763880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607537 | TTGAGCTAATTAACA[C/T]ATGCATTACCTCACA | 55666 |
rs542770836 | in-del | -/AAC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613139 | GCTAAAAAAAAAAAA[-/AAC]CAAAAACCGATAAAA | 55666 |
rs542784898 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628177 | GATCATGCCACTGCA[C/T]TCCAGCCTTGGAGAC | 55666 |
rs542926086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596710 | CTATGCAAACCACCC[C/T]GCCATGGGCTGAGCC | 55666 |
rs542946339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623574 | GAGGCCGAGGCAGGC[A/G]GATCATGAGGTCAGG | 55666 |
rs542980678 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632164 | TATTTTTAGTAGAGA[C/T]GGGGTTTCAACATGT | 55666 |
rs542983807 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617804 | CCTGCGATTGCAGGC[A/G]CGCGCCGCCACGCCT | 55666 |
rs542988386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628989 | GTTCACATCATTCTC[C/T]TGCCTCAGCCTCACC | 55666 |
rs543002869 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561523 | TACCCCAAGGTCCTG[A/C]ATCCTGCCTAAAAGA | 55666 |
rs543087618 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558266 | ACGCCCTCAGCCAGG[C/T]GGTGCAGTGGGACGA | 55666 |
rs543126722 | snp | A/G | 0.000329968 | 0.0128404 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600321 | CACGCCCCCTGCTTG[A/G]CTGCCGGATGCCTCA | 55666 |
rs543142757 | snp | A/G | 3.36553e-05 | 0.00410201 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604623 | CTCCGTGTACCGTCC[A/G]TATAAGTACCCAAAA | 55666 |
rs543143885 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629600 | ACTGTGATAGAGAAA[A/G]GCAATGCAAGAGGCA | 55666 |
rs543148483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616625 | GTCCCAGCTACTCGG[G/T]AGGCTGAGGCAGGAG | 55666 |
rs543156512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633936 | CAGTGGTGCGATCTC[A/G]GCTCACTGCAATCTC | 55666 |
rs543171116 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611717 | TGTAATCCCAGCACT[G/T]TGGGAGGCCGAGGCG | 55666 |
rs543188123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621954 | CAAATTCCAGAATTC[C/T]GCAAAGTCAATCAAA | 55666 |
rs543189835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562126 | AGTCCCAGCTACTCG[C/G]GAGGCTGAGGCAGGA | 55666 |
rs543226653 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584124 | ATTGGTGCAGGTTTT[A/G]TTTACAAGGCATGTC | 55666 |
rs543264191 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577038 | ATGAGTTACAGGGTC[A/C]ACCAAGTGCTGTTCA | 55666 |
rs543330061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612173 | CACAACACGCACAAT[C/G]TGAAGGAGAGGTATG | 55666 |
rs543388677 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570517 | CGGGGGCTCTTGCTG[A/G]CCTTGTAACTGGCCC | 55666 |
rs543406881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615850 | CAAAAAAAACCAACA[A/G]AGTCACCTCTGAGAC | 55666 |
rs543414434 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626860 | TTTGGGAGGCTGAGG[A/C]GGGCGGATCACCTGA | 55666 |
rs543447908 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575710 | CAGGGCCAGGGCACA[C/T]GCAGGCCTCCCTCCT | 55666 |
rs543451436 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594039 | AGCACCTTGGAAGGC[C/T]GAGGCGGGCGGATCA | 55666 |
rs543453013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626248 | TTGAACCCCGGAGGC[A/G]GAGGTTGCAGTCAGC | 55666 |
rs543494804 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610008 | GCCATTCATAATCCA[A/G]CGAGAAGGTCACTCC | 55666 |
rs543542447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570678 | AACCCACAAAGAAAC[C/T]CCAGTAACACTGGCT | 55666 |
rs543738309 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556851 | GATGCCAGACAACAG[C/T]TGAGTGCGCAGGAAG | 55666 |
rs543780170 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598710 | TGCACCAGAAGCCCG[A/T]CACGAGGCCACAGGA | 55666 |
rs543806250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560009 | CAAAGTGCTGGGATT[A/G]TAGGTATGAGCCACC | 55666 |
rs543879227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604378 | TACACTGAAGGTTTT[A/C]GGAGCCATGATCTCA | 55666 |
rs543911617 | in-del | -/A | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558515 | GACACAACCTCGGGG[-/A]GCTTCACTAAAGGAG | 55666 |
rs543913251 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616299 | GCACTCCAGCCTGGG[C/T]GACATAGCAAGACTC | 55666 |
rs543913749 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610830 | GGTGGCGGGCGCCTG[G/T]AGTCCCAGCTACTCG | 55666 |
rs543928621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576133 | TTGTTTTACAATGAA[C/G]AGTGGGACTAGGTCA | 55666 |
rs543930366 | in-del | -/C | 0.466721 | 0.124627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618593 | GAGGTGGGGGGTCAG[-/C]CCCCCGCCCAGCCAG | 55666 |
rs543934793 | snp | A/G | | | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563927 | CTCACGTACATAAAG[A/G]TGGCAACGCCAGGTG | 55666 |
rs543940130 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577031 | ACTAAGAATGAGTTA[C/T]AGGGTCCACCAAGTG | 55666 |
rs543952678 | snp | C/T | 0.000228163 | 0.0106785 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610195 | GCCCAGAACTTACTC[C/T]GCAGAGACTCTCACC | 55666 |
rs544000633 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604503 | GGGCGTCCCCCACAG[A/C]CTCCAAACACAGAAA | 55666 |
rs544005904 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564695 | CAGGAGGCTGAGGCA[A/G]GAGAATCGTTTGAAC | 55666 |
rs544015064 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636207 | AACTCCTGACCCCAG[C/G]TGATCCACCCGCCTC | 55666 |
rs544071085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604987 | ACATCTGGGCTGGGC[A/G]CAGTGGCTCACGCCT | 55666 |
rs544171406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620611 | GCAATGGTGACACAT[A/G]AGGTTCATCCATCAA | 55666 |
rs544184876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590960 | ACTCAAATGCTCAGG[A/G]GGCAGCCAACCCTGC | 55666 |
rs544237804 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558879 | CAGGGAGGCCAAACA[A/G]AAAGCACTGAAAATA | 55666 |
rs544246828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623730 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 55666 |
rs544247443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596651 | TTCCTAACCATTACC[A/C]ATTCCTCATCTAAAA | 55666 |
rs544249471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590359 | GCAGTGTGGTCCAGT[G/T]AGACCAGATCCCTGA | 55666 |
rs544297791 | snp | G/T | 0.215144 | 0.247558 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563171 | ACCTACGCTTCCTGG[G/T]TCAAGTGATTCTCCT | 55666 |
rs544373647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624460 | AAAAATTAGCCAGGC[A/G]TGGTGGTGCACGCCT | 55666 |
rs544404790 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592759 | GAGGCCGAGACAGGC[A/G]GATCACTTGAGGCCA | 55666 |
rs544435373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619245 | AGCCGGGCATGTTGG[C/T]GGGCGCCTGTAGTCC | 55666 |
rs544466960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592280 | CCGCATGGCCGTGAC[C/T]AAGAAACCCTAACAC | 55666 |
rs544490331 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585734 | CCCAGCATCTATAAT[C/G]CCAGCACTGTGGGAG | 55666 |
rs544493450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586990 | GGAGTCTCTGGCTTG[C/T]GATACACAATGAGCA | 55666 |
rs544523639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620261 | CCAGCACTTTGGAAG[A/G]CCAAGGCGGGTGGAT | 55666 |
rs544583162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628935 | CCAGGCTGGAGTGCA[C/G]TGGCGCGATCTCAGC | 55666 |
rs544612274 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602658 | AGTGAGTGGAGATCA[-/T]GCCACTGCACTCCAG | 55666 |
rs544613670 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558673 | ATCCCACCTGGACAT[C/T]GGGTGAGAGGAGGAG | 55666 |
rs544671593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573273 | GGAGCTCTCAGACCC[A/G]AAATGATTGCCAAGC | 55666 |
rs544796470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568228 | GACTTTTCCTGTCGA[A/G]CTGTATTCTCCATCT | 55666 |
rs544798958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580049 | GCCTGCCTTCCAGGG[C/T]GCTATGCTCCTGCCC | 55666 |
rs544808582 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573736 | CCTCCCAGAGAAAAA[A/T]GGTCCAAATAGATCC | 55666 |
rs544815866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574517 | TGTCAGTTGGAATGC[A/G]CTGGGAGGAGGTTGT | 55666 |
rs544869643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562266 | CATGAGGGCCGGGCG[C/T]GGTGGCTCACACCTA | 55666 |
rs544891476 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624921 | AAGAGATGAGGCTGG[C/T]GAGGCAGACAGGGCC | 55666 |
rs544924073 | in-del | -/AAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616733 | CAAGACTCCATCTCA[-/AAA]AAAAAAAAAAGAGTA | 55666 |
rs544935904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602032 | GTGCACATATTATAC[A/G]TACAAAGAAACAAAG | 55666 |
rs544958718 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612888 | GCTATGAAATGAGAG[-/AC]ACAGCACTCACCTCA | 55666 |
rs544972269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617786 | GCCTCAGCCTGCCGA[A/G]TGCCTGCGATTGCAG | 55666 |
rs544998038 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584005 | CCACATGCTATCCCA[A/C/G]AGTCCAGCTGTAACT | 55666 |
rs545065684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566203 | CAGGCGTGGTTGCGG[A/G]CACCTGTAATCCCAG | 55666 |
rs545138341 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638937 | CTAATTTGTTAGTCC[A/T]GAAAAGGCAGTCTTG | 55666 |
rs545138850 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618176 | TGGAAAGTGAGGAGC[A/G]TCTCTGCCCGGCCGC | 55666 |
rs545139034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612929 | GCACACACAACCACC[C/T]GCCCCTTCCCTCCTC | 55666 |
rs545156501 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557878 | GGAGGTGTCAGCCAT[G/T]GCCCTGACCACTTCA | 55666 |
rs545166544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623776 | GCACTCCAGCCAGGA[C/T]GACAGAGCGAGACTC | 55666 |
rs545196353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599214 | GAATCACTTGAACCC[A/G]GGAGGCAGAGGTTGC | 55666 |
rs545200818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560534 | TAACATGGTGAAACC[A/C]CGTCTCTACTAAAAA | 55666 |
rs545229570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607385 | CAGCTTTATTGAAAT[A/G]TAACTGACAAAAAAA | 55666 |
rs545310980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601115 | AGAGTGGACCAAGCT[G/T]ACCGAAATCATTAAT | 55666 |
rs545317368 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622359 | CACCAGACACTACTA[C/G]AAGAGTATTCACCAA | 55666 |
rs545355953 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625833 | TAGGAACCCATGGTA[C/T]AGGATCAAATGCTCC | 55666 |
rs545362050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634497 | CTTGTCAATGGTTAT[A/T]TTAACTCAGTTAAAA | 55666 |
rs545363907 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600556 | CAGAAAGGAGAACTA[C/T]AGCCACAGATAAAAC | 55666 |
rs545374105 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628871 | TCAACTGTAGTCATA[C/T]CTACAATTCATACTT | 55666 |
rs545400732 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620270 | TGGAAGGCCAAGGCG[C/G]GTGGATCACGAGGTC | 55666 |
rs545408196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622480 | TGAATAAAGTGGCCA[A/G]AAAAGCAAAGGTCTT | 55666 |
rs545412951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572451 | CCGCCTCAGCCCCCC[A/G]AAGTGCTGGGATTAC | 55666 |
rs545423110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571908 | ACTGCTCAAGGCAGA[A/G]GGTGCCTTAAATTGC | 55666 |
rs545453735 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566288 | AGTAAGCCAAGATTG[C/T]GCCAATGCACTCCGG | 55666 |
rs545472301 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599309 | AAAATAAAATAAAAT[A/G]AAAAGAGAAACTTGT | 55666 |
rs545480737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594168 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 55666 |
rs545485195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605953 | AGCCTCCTGAGCAAC[A/T]GGGACGACAGGCGCC | 55666 |
rs545499897 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612320 | TGTGCTTCCTAATAG[A/G]CAGGATCTAAGTGAT | 55666 |
rs545506843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593418 | CAGTCCAGAAGCACT[A/G]ACACACCTAAACGTA | 55666 |
rs545512122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81566558 | TAGGGAAGGCACAGG[A/C]AGGGAAGAGGCACAG | 55666 |
rs545532749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587767 | TCCGCCTCCCAGGTT[C/T]ACGCCATTCTCCTGC | 55666 |
rs545543777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616366 | TGCTAAATCTGGATC[C/T]TTCAGGATTCCTCAA | 55666 |
rs545567768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621149 | GAAAAAAAAAAGAAA[A/C]ATATCAAGATGCAAA | 55666 |
rs545599895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561254 | GAGCTACCATGCCCG[A/G]CCTGCATTTCCTTTT | 55666 |
rs545627936 | in-del | -/TGTGAGCTCACCCCCCATTCTCCTC | 0.0948562 | 0.196037 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579863 | CATGCAGCTTGCTGA[-/TGTGAGCTCACCCCCCATTCTCCTC]TGTGAGCTCACCCCC | 55666 |
rs545670336 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611671 | ATTTAAAGAAAAGTG[A/T]TAAATAGGCCAGGTG | 55666 |
rs545707225 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611050 | ATTGGCCAAAGGCAG[G/T]GGCTCACACCTCTAA | 55666 |
rs545707796 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617251 | AACAGACAGATTTAG[C/G]GGGAAAAAAAATCAG | 55666 |
rs545718566 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561209 | ATGATCCACCGCCTC[A/G]GCCTCCCAAAGTGCT | 55666 |
rs545718999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582495 | CAGCCGTGAACTCCT[A/G]GGCTAAAGAGATCCT | 55666 |
rs545736649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559958 | CAGGCTGGTCTCGAA[C/T]TCCTGACCTCAGGTG | 55666 |
rs545752983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625611 | GGTGAATAGCTTGTG[A/G]TCCCAGCAACTCGGA | 55666 |
rs545764086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565895 | GGAGCTCATGCCTCT[C/T]GTCCTGGAGGCTGGG | 55666 |
rs545801605 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563095 | TTTTTTTTTTTTTTG[A/G]GACAGAGTCTTGCTC | 55666 |
rs545817682 | snp | A/G | 0.000185925 | 0.00963993 | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637368 | TTATAGCGTATTATA[A/G]TTGGGGAAACAGCAT | 55666 |
rs545819543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630771 | GGTCTCAGCTACTTG[C/G]GGAGCTGAGGCACGA | 55666 |
rs545836113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580937 | TGCCCACAGCTGGGG[A/G]CCTGGGAGAGACATG | 55666 |
rs545837094 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613948 | TCACATACACACGTA[A/G]GCACAGACACGCATA | 55666 |
rs545861069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575350 | TCATGATCCACCCGC[C/G]TTGGCCTCCCAAAGT | 55666 |
rs545864395 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584728 | TTTACCTGTTTCAAA[C/T]ACCAACAGTTTAAAA | 55666 |
rs545898167 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587086 | ATTGCAGCTGCAGAC[C/G]CACATATGCTAACCC | 55666 |
rs545915928 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611337 | ATAAATAAATAAATA[A/C]AATAGTTTTTTTTTT | 55666 |
rs545916937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586340 | CCCAGCACTTTGGGT[A/G]GCCTCACGCCTATAA | 55666 |
rs545928461 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568132 | ACAGAGACACAAACA[C/T]GGAAATGCGCCCTGG | 55666 |
rs545934809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621794 | GGCCACTGCAGTGGC[A/C]GCACTCCTACCCAAG | 55666 |
rs545955099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582954 | ACCCAAGGAGCCTCC[C/T]GGCCAGGGCCAGGCC | 55666 |
rs545964804 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590806 | CCACACAATCAAAAA[A/C]GGTGAGGGAGGAGAT | 55666 |
rs545979816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570531 | GGCCTTGTAACTGGC[C/T]CTTGGAGGGGAACAG | 55666 |
rs545987476 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593327 | GCAAGGCCAGCTGAG[A/T]GGCCTGGACCCAGCC | 55666 |
rs545993004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573086 | GTTCAAACAGAGCTC[C/T]AGAAATAAATTCATA | 55666 |
rs546020065 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578058 | ACTCCTCTAAACTTG[-/C]TGCCTTCTCCTGACT | 55666 |
rs546043877 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590104 | TGTATACACAGCAGC[-/CT]CTGTCTTCCAGAAAC | 55666 |
rs546049592 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598093 | GAGCAAGACTCTGTC[C/T]CAAAAAAAAAAAAAA | 55666 |
rs546086643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571537 | GGGACCACCCTGGAC[A/G]GAGTGACCCAGACAC | 55666 |
rs546184946 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558478 | AGAACTGACTGGTGC[C/T]CCCGTCCACACTCAT | 55666 |
rs546192899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562317 | GCCGAGGTGGGTGGA[C/T]CACTTGAGGTCAGGA | 55666 |
rs546201384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634183 | TAATTTTTGTATTTT[C/T]AGTAAAGACGTGGTT | 55666 |
rs546208044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564986 | GCAGCAATGCTGACA[G/T]AAGGTTCTCACGAGT | 55666 |
rs546254625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609763 | TGAAGAAAATCGGGC[C/T]GGCCTTCCTGCTGTA | 55666 |
rs546268699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562955 | AAAAAAAAGGAGGGG[C/G]GAAAAAAAAAAGGTC | 55666 |
rs546280926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568290 | GCCGTGATGCAGCAC[A/G]GACATCTTCAGCAGA | 55666 |
rs546296686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615797 | AGCTGAAAATAGGAA[A/C]CAAGGAGGAATCCCA | 55666 |
rs546323074 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558763 | TCCCCACCAGACAAC[A/C]GCTACTAGAAGAGGA | 55666 |
rs546335361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615288 | TATTTTTAATAGAGA[C/T]GGGGTTTCTCCATGT | 55666 |
rs546369287 | snp | A/G | 0.249038 | 0.249998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564713 | GAATCGTTTGAACCC[A/G]GGAGGTGGAGGTTGC | 55666 |
rs546416145 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603672 | GTGAATACTCATATA[A/C]CCACCACTAGATTCA | 55666 |
rs546440567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624278 | CAAAAATTAGCTAGG[C/T]GTGGTGGCGGACACT | 55666 |
rs546483106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629028 | GGACTACAGGTGCCC[A/G]CCACCACACCCGGCT | 55666 |
rs546505536 | in-del | -/GTTTCTGCTTGTCTCTGAAGCTACTGAC | 0.45889 | 0.13735 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614569 | GAGTCAGACTTAAGG[-/GTTTCTGCTTGTCTCTGAAGCTACTGAC]GTACTGCTTTCCAAA | 55666 |
rs546505632 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591103 | CTGGACAGAGCGCCG[C/G]GGAGCCACGGTGCAG | 55666 |
rs546519012 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597098 | AGCCTGGGCAAAAGA[A/G]CAAGACTCCGTCTCA | 55666 |
rs546558578 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636736 | GGGACACGGACGGGA[A/G]GCAGCCGAGGGGGGT | 55666 |
rs546591806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585589 | ATCGCAGAACTCAGG[C/T]GGCAGAGGTTGCAGT | 55666 |
rs546604007 | snp | C/T | 0.000160038 | 0.00894391 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610161 | TAAGACAGCTGTCTA[C/T]CCGCAGCCCCCCACA | 55666 |
rs546654484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595444 | AAAAAAAAAAAAAAA[C/T]CCGTTTTGCTTTTTT | 55666 |
rs546717218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617458 | GCCAGCAGATCACCT[A/G]AGGTTAGGAGTTCAA | 55666 |
rs546717242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623175 | CTCCAGCTTGGGCAA[A/C]AAGAGCAAAACTCTG | 55666 |
rs546718752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628500 | CCTGGGCAACAGAGT[A/G]AGATGCCATCTCAAA | 55666 |
rs546728439 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584222 | TTGCTCCAACTGATA[A/T]TTTCCTGAAACATGA | 55666 |
rs546907208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614144 | TAGCTGGGCGTGGTG[A/G]CGCACGCCTGTAGTC | 55666 |
rs546922501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572929 | GAAGACACGGGAACC[C/G]CACACCAATCTGTCA | 55666 |
rs546931565 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575607 | CCTCCTAAAGCAATC[A/G]GCAAGGACAGCTGGA | 55666 |
rs546941956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618879 | AAATTCTTCTGCCTT[A/G]GGATCCTGTTGATCT | 55666 |
rs546964169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577116 | CTGGCCACAGCAAGG[C/G]GCAGTGGGTTCCTCA | 55666 |
rs546965291 | snp | G/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615189 | ACTGGAACCTGCATC[G/T]CACGGGTTTAAGCGA | 55666 |
rs546997416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589258 | GTAGTCGGCCGGGTG[C/T]GGTGGCTCATGCCTG | 55666 |
rs547024237 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631799 | ATCTCTTGTATTTAG[C/G]TCATTTTTTTTTTCC | 55666 |
rs547028021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576642 | AAAAGACAAAGAACG[A/G]AAACCTGGCGTGTGT | 55666 |
rs547040757 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558032 | GCAGAGCAGCCCAGA[C/T]GTGGCCATCATTAAG | 55666 |
rs547051732 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611335 | AAATAAATAAATAAA[C/T]AAAATAGTTTTTTTT | 55666 |
rs547053746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571732 | CCTGGGGTCAGTGGT[C/T]CTTTGTACTTTAGTA | 55666 |
rs547123339 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613229 | CTTCATCAGATACTT[A/T]TTAAAACAAGACATG | 55666 |
rs547128491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605206 | GAATGGCGTGAACCC[A/G]GGAGGTGGAGCTCGC | 55666 |
rs547153325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599327 | AAGAGAAACTTGTGT[C/G]TTGCAGAAAATTATT | 55666 |
rs547169421 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564317 | GCCCCAAGAATTAGC[C/T]GGGTGTGGTGTTGCA | 55666 |
rs547256350 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632991 | AAACATTAGCCAGGC[A/G]TGGTGGAGGGCGCCT | 55666 |
rs547258882 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578501 | CTATAATGAACTGCC[C/G]AAGACTGGGTAATTT | 55666 |
rs547284139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607016 | AATCCCAGCTTCTGT[C/T]CCACATACTTCAACC | 55666 |
rs547291129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599868 | AATGATGATTGATGA[C/T]GGAGCAGCAGAAGCT | 55666 |
rs547313014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600781 | TACTTTCAAACTTCC[C/T]TGGATAAGTAGCTTC | 55666 |
rs547380605 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587954 | TGCTGGGATTACAGG[C/T]ATGAGCCGCCGCGCC | 55666 |
rs547385419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559489 | AGTGTGGGCATGGGG[A/G]CAGGGGCAGGCAGCT | 55666 |
rs547387477 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564799 | GTCTCAAAAAAAAAA[A/C]AAAAAACAGGAAATG | 55666 |
rs547388381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622934 | GCGTGGTGGCTCATG[C/T]CTGTAATCCCAGCAC | 55666 |
rs547417316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627114 | AAAGAAAAAGGGCCA[G/T]GTGTGGTGGCTCACT | 55666 |
rs547457414 | in-del | -/TTA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599653 | AAGGATAAAACATAC[-/TTA]TTAACATTAAACTCG | 55666 |
rs547521332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559774 | GTCTTGCTCTGTCAC[C/G]CAGGCTGGAGTGCAG | 55666 |
rs547593657 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81639056 | TATTTCAGCCTACAC[C/G]CAGGAATGAACAAGG | 55666 |
rs547616869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631100 | ATCGCTTGAACCCAG[A/G]AGGCAGAGGTTGCAG | 55666 |
rs547620020 | snp | C/T | | | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81564231 | GGTGACAAACCTGCA[C/T]ATGTACCCTGTGAAT | 55666 |
rs547628557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638567 | CCTCCCCAAAGTGCT[A/G]GGACTATAGACGTGA | 55666 |
rs547639864 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598668 | TGTGCTGTGTGATCC[A/T]TAGGCCCGCCTCTGC | 55666 |
rs547696994 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556419 | GAGGCTCAGAGAGCA[C/T]TTGTTCTAGACGCTT | 55666 |
rs547697926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582295 | GCACGTCACATCCGT[A/G]CCAGGAGGTTTTCAG | 55666 |
rs547701300 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587290 | ATCAACCTGGCCAAC[A/C]TAGTGACACCCTGTC | 55666 |
rs547749943 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557698 | CCGCGGTGGGCAAGC[C/T]GGGAGTTGCATCCGC | 55666 |
rs547772824 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570828 | TCAAGGACTCCCCAT[G/T]CCTCACTTCCACAGG | 55666 |
rs547773949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604447 | GTGTGTGACAAAGGG[A/G]GAACAAACAACAAAG | 55666 |
rs547789147 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636523 | TCAGAGGGAGATTAG[C/G]ATAAGAGGTGTCCCT | 55666 |
rs547892263 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569342 | TATCCGGGCAGCCTC[C/G]GGCCTGTGCACCGGC | 55666 |
rs547915388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598414 | AGGCACTTAAACTCC[C/T]AAGAGGAAGACAGAC | 55666 |
rs547926562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625132 | TCATCACCAGGCCCA[A/G]CTGACGAGCAGGACC | 55666 |
rs547930343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619615 | CAGGCGCAGTGGCTT[A/G]CATCTGTAATGCCAA | 55666 |
rs547936924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626350 | AGAATGAAAATAGAA[C/T]AGAAAAATACTTAAG | 55666 |
rs547954177 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560188 | TTTGGGAGGCCGAGG[A/C]GGGTGGATCACTTGA | 55666 |
rs547974275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631846 | ATCTTGTGGCCCAGG[A/C]TGGAGTACAATGGCG | 55666 |
rs547991389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620302 | GGAATTCGAGACCAG[C/G]TTGGCCAACTTAGTG | 55666 |
rs547996750 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593649 | CTACACTACTGTACC[C/G]AGATATCAGCCTACA | 55666 |
rs548014192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625877 | ATGAGGGTTGGGCGC[A/G]GAGGTTCAAGCCTGT | 55666 |
rs548053023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615499 | CAATTTTAACAAATA[C/T]ACTCTAAAATCAATT | 55666 |
rs548059467 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575455 | CAGTCCGTGTGCAAC[A/G]ACTGGATGCACACAG | 55666 |
rs548083585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587927 | TGATCCGCCCATCTC[A/G]GCCTCCCAAAGTGCT | 55666 |
rs548097895 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595835 | AGGCGTGAGCCACCA[A/C/T]GCCCGGCCAAAAAAG | 55666 |
rs548221609 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559076 | AATACCAGCCGTGGC[A/G]CCCGCTCTCCAGGGA | 55666 |
rs548258071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581241 | CCTGTAATCCCAGCT[A/G]CTTGGGAGGCTGAGG | 55666 |
rs548262250 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586541 | CTTGAACTCAAGGGG[C/T]GGAGGCTGCAGTGGG | 55666 |
rs548262725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618806 | AATCGGATGGTTGCT[C/G]TGTCTGTGTAGAAGG | 55666 |
rs548273465 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608389 | AGCCAGGCGCCTGCA[C/G]AGTCGCTCTGCCTTG | 55666 |
rs548322568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586076 | GGTCACTTGAGATCA[C/G]GAGTTCGAGACCAGC | 55666 |
rs548349785 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627925 | TGGGCGACAGAAAAA[C/G]ACTCCATCTCAAAAA | 55666 |
rs548402235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575185 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAA | 55666 |
rs548419070 | snp | C/T | | | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565268 | TACAGGTTTATAAAA[C/T]TTACAGGGCTGTGTA | 55666 |
rs548429279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614005 | TGACTGGCCAGGCTC[A/G]GTGGCTCATGCCTGT | 55666 |
rs548461487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610312 | GGATGTCTGTGTTCC[A/G]CTGCTGCTGTCTCAC | 55666 |
rs548502081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603849 | TTGCTTACTTTTTTA[C/T]TTTTGCAATAAAATG | 55666 |
rs548551745 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589527 | TGGGTGACAGACTCC[A/G]TCTCAAAAAAAAAAA | 55666 |
rs548556113 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635732 | TTCTAGACAACACCT[C/G]GCAAAACTGCAGAGA | 55666 |
rs548568375 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567848 | CACTTTTTAGGAGGC[C/T]GAGGCAGGCAGGTGG | 55666 |
rs548576341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618430 | GCCCCGCAGCCGCCC[C/T]GTCTGGGAAGTGAGG | 55666 |
rs548627398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568413 | ATCAAAGCATAGAAG[A/C]AGCTTTGTCAGCCAC | 55666 |
rs548627472 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557587 | AGCAATGCAGGAAGC[C/T]TTGGCCACCTAGGCT | 55666 |
rs548668412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600034 | GGGGTCTGTTTCCCA[C/T]TTGAAGCAGTCCTCA | 55666 |
rs548729153 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572749 | TGCGTTCCCCTCAGG[C/T]TGGACCTGTGCCCTG | 55666 |
rs548758409 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635138 | CGAGGTCAGAAGTTC[A/G]AGATCAACCTGGCCA | 55666 |
rs548769380 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633485 | AGGTTTCCAAGGCCA[A/G]CTCCAGTATTTAACA | 55666 |
rs548819234 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585038 | AGCCAGGCGTGGCAG[C/T]GTGCGCCTGTAGTCC | 55666 |
rs548822240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629271 | CACCTCGACTCACTG[C/T]AAACTCTGCCTTCTG | 55666 |
rs548855071 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591278 | TGTCTCTACTAAAAA[C/T]ATAAAAATTAACTGG | 55666 |
rs548857354 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558723 | TGCAGACCTGCAGAG[C/G]GGAGCCGTGTCCAGG | 55666 |
rs548867233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596986 | GGCATGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 55666 |
rs548918330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611612 | GCCTCAGCCTCCCAA[A/G]GTGCTGGGATTACAG | 55666 |
rs548937121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595907 | GGAGGTCCTGATTCT[A/G]TTATGAGTTTTGGGG | 55666 |
rs548948095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627057 | ATTGTGCCGCTGCAC[C/T]CCAGCTTGGGCGACA | 55666 |
rs548963325 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636036 | GGAGTGCCATGGAGG[A/G]ATCTCAGCTCACTGT | 55666 |
rs549023078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590487 | CTGAAGTTATGTGCT[C/G]ACTACAATCTCATTA | 55666 |
rs549053716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595304 | CCAGGCGTGGTGGTG[C/T]GCACTTACAATTCCA | 55666 |
rs549124639 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557208 | CCTTCCCACAAGAGG[A/T]GGTGGCTGAGCCTCC | 55666 |
rs549127403 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584639 | TGGAAAGGATAATAC[A/G]TGTAGGAAATGCGAA | 55666 |
rs549142741 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558164 | CGTGCTGTTCCAGAT[C/T]GCCCAGTCTCCCTCT | 55666 |
rs549173059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622553 | AACAAGAGTTAATGG[A/C]TATCCTTGTTTTGTT | 55666 |
rs549185100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623267 | ACGAGGCCAGGAGTT[C/T]GACACCAGCCTGGTC | 55666 |
rs549219526 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627985 | TGGGAGGCCAAGGCG[A/G]GCAGATCACGAGGTC | 55666 |
rs549259716 | snp | A/G | 0.00079674 | 0.0199433 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622120 | GGGCAGATCATGGGG[A/G]CCTCATTTCCCCCCA | 55666 |
rs549372984 | in-del | -/A/AA | 0.494315 | 0.0530107 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634447 | TTATACACTAGTGGG[-/A/AA]AAAAAAAAAATGGCC | 55666 |
rs549378552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632770 | ACAAAACACCATAAA[A/G]GCTCAGTCTACTGGG | 55666 |
rs549380624 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560655 | GAGGTTGCAGTGAAC[A/C]GAGGTTGCAGTAAGC | 55666 |
rs549409134 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595839 | GTGAGCCACCACGCC[C/T]GGCCAAAAAAGTGGA | 55666 |
rs549435377 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625092 | TGGTGGGGATGAAGG[-/C]CAAGAGCACACTTTC | 55666 |
rs549449103 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558935 | TCGGCCCCTCCCTGT[A/G]CGCCCCAATTCCAGG | 55666 |
rs549515239 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588741 | GCATGTAGCTCCACT[G/T]CTGGTGAGAAGCCCT | 55666 |
rs549625843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572842 | CACCTCTGAAAACCC[A/G]ACTTTCCAGAAACCG | 55666 |
rs549683564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605589 | GGAGGCTGAGGTTGC[A/G]GTGAGCCAAGACTGC | 55666 |
rs549761195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570110 | GATTTGCTGTGCCAG[C/T]GCCAGCCGCTGTGGA | 55666 |
rs549763161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564435 | ACTGCACTCCAGCCT[C/G]GGCAATAGAGTGAGA | 55666 |
rs549774164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569504 | GGAACGGAAGGGCCA[A/G]GAGGCCGCCCCAGGA | 55666 |
rs549779424 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560796 | TGAGACACAGTTCTC[A/G]CGAGGGTGGCACGGT | 55666 |
rs549822040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576461 | GAAGGATCCACTTTG[A/G]GGCGTGAGTGCATGT | 55666 |
rs549873857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571171 | GGGGACCTGCTGTTC[C/T]GAATGCAATGATATT | 55666 |
rs549919968 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582097 | AATCACCAGAAAACA[C/T]GGAGCATAGACAGAG | 55666 |
rs549951421 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586061 | AGGCTGAGGTGGGTA[C/G]GTCACTTGAGATCAG | 55666 |
rs549994745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592627 | GGTGGTAGCCCCCAA[A/G]TTAGAAACTGTAATT | 55666 |
rs549997949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565806 | GAACTAGAATTTAAA[C/T]TCTTCCCAAATAGGC | 55666 |
rs550001402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597640 | AAATACAAAATTAGT[C/T]GGGGTGGTGGCGCAT | 55666 |
rs550007352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638415 | GTGATTCTCCTGCCT[C/T]AGCCTCCCGGGTAGC | 55666 |
rs550012440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571671 | GATGCTCCGGTGACT[A/G]GAGACCCAAGCAATG | 55666 |
rs550042031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599269 | ACTCCAGCCTGGGTG[A/G]AAGAGCAAGACTCCT | 55666 |
rs550080330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593033 | TCACTCAGAATAAAA[C/T]AGTCATTAAAACCAC | 55666 |
rs550082188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586663 | CATGGGATACCTACA[C/T]ATTTAAGCTGTATGA | 55666 |
rs550144169 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635853 | AATGCTCCTGTCCAA[G/T]GGTCAGTTAGTTTTT | 55666 |
rs550147411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629130 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 55666 |
rs550156332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575392 | AGGCGTGAGCCACAG[C/T]GCCCAGCTGACACTT | 55666 |
rs550158721 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632793 | CTACTGGGATTTGTC[C/T]GCTTTTAGTAAAGTA | 55666 |
rs550184223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635123 | AAGGCGGGCGGATCA[C/T]GAGGTCAGAAGTTCG | 55666 |
rs550254382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597393 | CAGTGACTCACGCCT[A/G]TAATCACAGCACTTT | 55666 |
rs550263435 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558938 | GCCCCTCCCTGTGCG[C/T]CCCAATTCCAGGTGC | 55666 |
rs550309157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629572 | ACATCTCATCCTATA[A/G]CAATCCAACCCAACT | 55666 |
rs550330337 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558585 | TGCAGTTTTTATCTT[-/A]AAAAAAAATAAATAA | 55666 |
rs550338933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596848 | GGCTGGGCATGGTGG[C/T]TCACACCTGTAATCC | 55666 |
rs550372027 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636886 | TGCCTCATCCCGGCG[C/T]CCCCGCTCCCGCCCG | 55666 |
rs550382259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598277 | TGTTCAGTAGAAACT[A/G]GCCACCCTCCCTCTG | 55666 |
rs550385073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630975 | GTCAGGAGTTCGAGA[C/G]CAGCCTGGCCAACAT | 55666 |
rs550420219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630457 | ACACCAGGTTAATTT[C/T]TTTTTTTGTAGTGAC | 55666 |
rs550473770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619448 | CAGCTACTCGGGAGG[C/T]TAAGGCAGGAGAATC | 55666 |
rs550489893 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581175 | GCCAACATGGCGAAA[A/C]CCTGTCGCTACTAAA | 55666 |
rs550494949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620457 | GCTGGGATCACGTCA[C/T]TGCACTCCAGCCTGG | 55666 |
rs550563841 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618353 | GCCTGGCCGCGACCC[C/T]GTCTGGGAGGTGAGG | 55666 |
rs550566932 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558806 | CAGGCAGGGTGCCTG[C/T]CACCAAGCAGTCAGA | 55666 |
rs550575727 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575159 | GGCTGGAGTGCAGTG[C/G]CGCGGTCTCGGCTCA | 55666 |
rs550652717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591912 | CGTAAATGTAGAGTA[C/T]GCTAGACTATGAGGA | 55666 |
rs550654887 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607094 | CCATCTATCACTAAC[A/G]TCCGAGAAAGCTTTC | 55666 |
rs550657119 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609655 | TTCAAGATTAAAATG[A/C]ATCTCTATTAAACAC | 55666 |
rs550691039 | snp | C/G | 1.68459e-05 | 0.00290219 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613276 | TTATTCACCCATTAA[C/G]ATCACCACAAGTAGG | 55666 |
rs550703514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627984 | TTGGGAGGCCAAGGC[A/G]GGCAGATCACGAGGT | 55666 |
rs550715142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591144 | AGGACACCATGAAAA[C/T]CTGGACTGGGCTTGG | 55666 |
rs550718277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607864 | GTCAGAGAAAAGCTA[C/T]AATCAGGCGAATATG | 55666 |
rs550751606 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601170 | TCATTCAAAGGTATC[A/G]TTCTATGCAGAAACC | 55666 |
rs550764570 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614261 | CAGCCTGGTGACAGA[C/G]GGAGGCTCCATCTCA | 55666 |
rs550800785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580398 | TCCTTTTCCAGCTCC[A/G]AGCCCAGCAGCCAGA | 55666 |
rs550828397 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578402 | ACCATGAGGGACCTG[C/T]TCACCGTGGCGCCCC | 55666 |
rs550839333 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586019 | GTCAGGCACAGTGTC[C/T]CATGCATGTAATCCC | 55666 |
rs550876963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628135 | AGAGTGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 55666 |
rs550886463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615405 | ACGTCCAGCCGAGAC[A/G]TCTGTTTCTAATAGC | 55666 |
rs550888613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609163 | TAGCTAGGACTACAG[A/G]TGCACGCCACCACGC | 55666 |
rs550934244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578801 | AGATGAGGTGTGGGT[A/G]TGGACACAAAGCCTA | 55666 |
rs550956508 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623197 | AAAACTCTGGCCGGG[A/T]GTGGAGGCTCACACC | 55666 |
rs551083854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566293 | GCCAAGATTGCGCCA[A/G]TGCACTCCGGTCTGG | 55666 |
rs551094414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566819 | AAAAAGCCAAAGTCG[A/G]ACCCCTACACACGGC | 55666 |
rs551104679 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600014 | GAGCCAGCAGGGGTG[C/T]GGCTGGGGTCTGTTT | 55666 |
rs551193495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568375 | AGCACCCCAAGTCCC[A/C]TGGGCGGATGGGCAC | 55666 |
rs551195131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594900 | TGAGCTATGACTGCA[C/T]CACTGTGCTCCAGCC | 55666 |
rs551196201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599506 | TTCTTTCCTAAAGAC[A/G]GTAAAACTGTGTGGA | 55666 |
rs551203714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573974 | GCTTCCGCATTCTGC[A/G]CTCTGCTGGCTGTGA | 55666 |
rs551231004 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622618 | TACAGTGGCATGATC[G/T]CGGCTTACTGCAACC | 55666 |
rs551264216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601442 | GTGTGTGTATTTTTA[A/G]TAGAAACGGGGTTTT | 55666 |
rs551267617 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602555 | TAAAATTACAAAAAT[C/T]AGCCAGGCGTGGTGG | 55666 |
rs551282854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589346 | CCATCCCGGATAACA[C/T]GGTGAAACCCCGTCC | 55666 |
rs551285154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595177 | CTATGATTACAGATG[C/T]TGTAATCCCAGCACT | 55666 |
rs551305793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562305 | GCACTTTGGGAAGCC[A/G]AGGTGGGTGGATCAC | 55666 |
rs551307777 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584289 | TCTGGGAAGTATTTC[C/T]AGCCTATTCTCGCTA | 55666 |
rs551350847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612413 | ACAGATCATGCAAGC[A/G]AGCCAGTGCCAGGCC | 55666 |
rs551374961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637746 | CAAGACCAGCCTGAC[C/T]AACGTGGTGAAACCC | 55666 |
rs551396126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638689 | GGTGAAATGATAGGG[A/G]GTCAAAACTGTCCTC | 55666 |
rs551470470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606268 | AGGCTACTCAGAGGC[A/G]GGACAAGGACAGCAG | 55666 |
rs551492237 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557054 | GCCCCACCTCCTCTC[A/G]GGACCAGGAGACTGG | 55666 |
rs551532697 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619187 | TCTGCGAGAAACACC[C/T]AAGAATGATCAATTA | 55666 |
rs551541361 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576739 | CTTTACAAATACTTA[A/T]GTGCACACAGAGGCT | 55666 |
rs551558419 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558057 | ATTAAGGCAAAGAAG[C/T]ATCGAGATGCCCACC | 55666 |
rs551572266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561821 | GTGGGCTGGTCTCAC[A/G]CTTCTGGGCTACAGT | 55666 |
rs551578941 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634022 | GTGCACGCCACCACG[C/G]CCGGTTAATTTTTTG | 55666 |
rs551582414 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557417 | TGCCGGAACTTCAGA[A/G]TAAGGGAAATGCTGG | 55666 |
rs551587135 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627538 | TGAGGTCAGGAGTTC[C/G]AGACCAGCCTGACCA | 55666 |
rs551597393 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631034 | AAAAATTAGCTGGGC[A/G]TGGTGGCGGGCACCT | 55666 |
rs551623206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626419 | TAGCAACTCCAGGAA[C/G]TTCAGCAAACTCTCT | 55666 |
rs551656324 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559886 | TACAGGCATGAACCA[C/T]AATGCCTGGCTAATT | 55666 |
rs551681869 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627434 | GGAACAAAAATGAAC[C/T]GTCAACTCAGAAATC | 55666 |
rs551724929 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620417 | AGGAGAAATGCTTGA[A/C]CCCGGGAGGCAGAGG | 55666 |
rs551736372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582798 | TGTCCCTGTGTGATG[C/G]GCAGGAGGTCCCAGC | 55666 |
rs551820562 | snp | C/G/T | 6.67695e-05 | 0.00577762 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596075 | AACAAAATATATTAA[C/G/T]GAGGTGGTAATATTT | 55666 |
rs551843896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616106 | GGAGGATCACGAGGT[C/T]AAGAGATTGAGACCA | 55666 |
rs551871533 | snp | A/G | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581697 | CCAGCCAGCAAGGTG[A/G]TAAAGGCACAGCTAC | 55666 |
rs551878136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620750 | AGCGGGACAAGCGTG[G/T]TCGTGAGCTGAGAGT | 55666 |
rs551883794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615539 | TAAAGAAAGTAGAGG[A/G]AATCCCCAGGGGACA | 55666 |
rs551920097 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622078 | TGAGTGGTGTGATGA[A/G]GAAAGAGGATAAAAC | 55666 |
rs551927440 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593751 | CGCTGGCCAGGCAGA[A/T]TTCTAAATGACATGA | 55666 |
rs551936769 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583038 | AGCACAGCAGCCACT[A/G]CCACGTGACGCAGAG | 55666 |
rs551959029 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559021 | TAGGCGTGAGGAGCC[A/G]CTCTGCGTTTCCAGT | 55666 |
rs552004542 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637176 | GGCTCGACGCATGCG[C/T]AGGGCGGCGCCGCTG | 55666 |
rs552038388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610390 | TATTCCAGATGGCAC[A/G]TGGATAAACATTTAT | 55666 |
rs552093270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611754 | TCACAAGTCAGGAGA[C/T]AGAGACCATCCTGGC | 55666 |
rs552133067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575097 | AAGCTTTCAGACACT[C/T]GGTTACTTTTCTTTT | 55666 |
rs552149440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568638 | ACACACGGGAAAGCC[A/G]AGGCCAGGCCGAGAG | 55666 |
rs552154986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565169 | AGGTCCCACGCTTCC[A/G]GCGCTTCCATAAAGT | 55666 |
rs552212742 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595911 | GTCCTGATTCTGTTA[C/T]GAGTTTTGGGGTTTG | 55666 |
rs552219962 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586414 | CAGGAGTTCAAGACC[A/G]GCCTGGCCAACATGG | 55666 |
rs552241659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609938 | ATCGGAAAAGGATTG[C/T]CCAGGGAGCCCGCTG | 55666 |
rs552355234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569427 | CAGAGTCACACAGGT[C/T]CTCTCCCTCTGCTAT | 55666 |
rs552389747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603004 | ACACACACACACACA[A/C]ACACACACACATATA | 55666 |
rs552390573 | snp | C/T | 6.62515e-05 | 0.00575512 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81597292 | GGGTATCTTCTGAGA[C/T]GAGGTCTGTAAATAT | 55666 |
rs552404193 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608939 | GCAAGTCAAGGCCCA[A/C]AGTGAAAGCAGGTAC | 55666 |
rs552407531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570261 | TAGGGATCCTGGGCC[C/T]CACTTTACTCTTCCT | 55666 |
rs552442623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575837 | TTTCTCTTAAGACTG[A/G]GAATATGCTATAATA | 55666 |
rs552476721 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597526 | GCGGTGGCTCACGCC[C/T]GTAATCCCAGCACTT | 55666 |
rs552495875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608486 | GAAACCAAGGCAGGA[C/G]GATCACTTGAGCCAA | 55666 |
rs552496456 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598532 | AAGGGGTAATATAAT[A/G]CAGACTTCACACAGC | 55666 |
rs552555046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614674 | GTGTGTTCTTCCCTT[C/G]GTCAGAGTCACGCTG | 55666 |
rs552608493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563614 | AAAAGACTGGTGTCA[C/T]TGTTAGAACTGCATC | 55666 |
rs552707707 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624396 | GCACTCCAGCCTGGG[C/T]GACAAGAGTGAAACT | 55666 |
rs552713814 | snp | A/G | 1.65872e-05 | 0.00287981 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629682 | GGCAGTAAGAGTAGA[A/G]GATGAAAAATATCCT | 55666 |
rs552729526 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599656 | GATAAAACATACTTA[C/T]TAACATTAAACTCGT | 55666 |
rs552732936 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573678 | CCCTCACACCTTTTC[A/T]CTACTCACAGCTAGA | 55666 |
rs552752855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559955 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 55666 |
rs552781080 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636323 | CATTTACAACATTCC[G/T]TTTAAAGAGGAATTG | 55666 |
rs552796367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586119 | GTAGGAGGGAGGAAG[G/T]GGAGGCAGGGGCCTG | 55666 |
rs552799411 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559097 | TCTCCAGGGAGGAAC[A/G]TGCTGAGAAGCTTCA | 55666 |
rs552814150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575658 | CCCCCACACTACGTG[C/T]GCAGGCTCCCCGCCT | 55666 |
rs552816980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590115 | CAGCCTCTGTCTTCC[A/G]GAAACCTACACGGCC | 55666 |
rs552819629 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635788 | TTACTCTTCACCCAA[C/T]ACTGCTAAGCTTCCC | 55666 |
rs552836555 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607000 | GTTCCAGCACATTCC[A/G]AATCCCAGCTTCTGT | 55666 |
rs552838415 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573899 | AAATGACTTTCCACC[A/G]ACTTGGGTGAGGGTC | 55666 |
rs552871505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624788 | GCGGTGGGTAAGCCC[A/G]CCACACGCGAGCTGG | 55666 |
rs552882577 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596378 | TTTGAGAGGTGGAGG[C/T]GGGAGGTCCACTTGA | 55666 |
rs552912535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616923 | CCAAAATGACCAGGC[A/G]GGATTCTAGGACATG | 55666 |
rs552951270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616580 | CTAAAAATAGAAAAA[A/G]TTAGCCGGGCATGGT | 55666 |
rs552951398 | snp | A/G | 1.65622e-05 | 0.00287764 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622201 | GGATTTGTTGGAGGA[A/G]GCTGTTATCTCTCCG | 55666 |
rs552967448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589561 | AAATTCAGTAGTCAA[C/T]GGATGGGTGGCCACA | 55666 |
rs552982683 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608112 | TGGCTGAGCCTGTGG[A/G]CAACTACTGTGGTAC | 55666 |
rs552985158 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622895 | ATTTTTGAATTCAAT[A/T]GTAAAAACCCAATTC | 55666 |
rs553056425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611630 | GCTGGGATTACAGGT[A/G]TGAGCAACTGCGCCT | 55666 |
rs553100027 | snp | C/T | 0.00385247 | 0.0437195 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613393 | TCATCCTCCACCACG[C/T]TGGGAGCGCCAAAGA | 55666 |
rs553146872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617729 | AGCTGGACTGTACTG[C/T]TGCCATCTCGGCTCA | 55666 |
rs553146936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623361 | TAATCCCAGCTACCC[A/G]GGAGGCTGAGGCAGA | 55666 |
rs553210000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618093 | CCCCGTCTGGGAAGT[A/G]AGGAGCCTCTCTGCC | 55666 |
rs553221293 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557876 | CTGGAGGTGTCAGCC[A/G]TGGCCCTGACCACTT | 55666 |
rs553242466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606489 | GAGAACTGAGGGCGC[A/G]CACTCCATATCTCCA | 55666 |
rs553255203 | in-del | -/CAGAGGAGACAG | | | cds-indel, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557621 | AGCTCATCTCAGGAC[-/CAGAGGAGACAG]CAGAGGACAAAACTT | 55666 |
rs553257331 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576901 | CCTGCAAGTGTCCAC[C/T]CTGCCACATTCCCAG | 55666 |
rs553302854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604865 | TGTGATGGTGCATGC[A/C]TGTGGTCCCAGATAC | 55666 |
rs553309676 | in-del | -/AAA | 0.338523 | 0.233803 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616730 | GCAAGACTCCATCTC[-/AAA]AAAAAAAAAAAGAGT | 55666 |
rs553330769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613803 | GCTGGGTTTCAGGGC[C/T]TCTCCTCCCGCCTCT | 55666 |
rs553427591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598995 | AATTAGGGCTTAGAA[A/T]CTCATATTTTAGGCC | 55666 |
rs553428979 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605289 | CCATCTCAAAAAAAA[A/T]AAATAAATAATAATA | 55666 |
rs553459904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611954 | GACAGAGCGAGAGTC[C/T]ATCTCAAAAAAAAAA | 55666 |
rs553462566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598674 | GTGTGATCCTTAGGC[C/T]CGCCTCTGCCTGTGA | 55666 |
rs553463291 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600320 | CCACGCCCCCTGCTT[C/G]GCTGCCGGATGCCTC | 55666 |
rs553538989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631507 | GATCTGGAAGACTAC[C/T]GGACAAAGGGCATTA | 55666 |
rs553564892 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562710 | TCTCAGCACTGAGGC[A/G]GGAGGATCGCTTGGG | 55666 |
rs553574468 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81566497 | TGTCCAGACAGATGG[A/G]CAGCAGCTGAACCTC | 55666 |
rs553577408 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599735 | CTGGGAACTGTATCA[A/G]TGTCAGATAAACCAG | 55666 |
rs553697553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626184 | AGCCAGGTGAGCTGG[C/T]ACGTGCCTGTAATCT | 55666 |
rs553713227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594571 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 55666 |
rs553719916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587651 | AAAAAAAAAAAAGGA[A/G]AAAAGAAACAAAGAA | 55666 |
rs553761278 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559171 | GGCTGCCCACTATGG[C/G]GCAGTTACAGGGAAC | 55666 |
rs553772340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571232 | TCAAATGCAGCCTGA[A/C]TAGATCCTGGCGTGG | 55666 |
rs553841231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581444 | GTGCCCAATTGTTAC[G/T]TGTCCTCAAGAGGCT | 55666 |
rs553868782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559897 | ACCACAATGCCTGGC[C/T]AATTTTATCTATTTT | 55666 |
rs553897428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630024 | AGAGTACTGTCCTCT[C/T]AACTCTTAGTTTCAC | 55666 |
rs553912796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626712 | CTCACGTGGGAGGAT[C/T]GTTTGAGCCCGGGAA | 55666 |
rs553950832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632277 | ACCAACCCTGGCCTA[A/G]CTGATTTTTTATAGT | 55666 |
rs553971914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581967 | TGTCTCTGGGACGTG[C/T]TGACAGCAGAGACAT | 55666 |
rs553976593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586320 | GCAGCTGGGTGTGGT[A/G]TAATCCCAGCACTTT | 55666 |
rs554007513 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557254 | CACAGCAGGGCTCAC[C/T]CCCAAGCCTGTATGC | 55666 |
rs554018056 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556619 | GGCTGACAGGTGCGG[C/T]AGAGGCAGAAGAGGC | 55666 |
rs554037165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588296 | ACCAAAAAGAGAAAA[C/T]ATTGAGTAGCTGCAA | 55666 |
rs554099064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582926 | GCCTCCCGATTCGAA[C/G]AAACACACAAAAACC | 55666 |
rs554124284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570457 | TAGAAATGAAGAAGG[C/T]GGCACCCCCAGAACA | 55666 |
rs554128980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619107 | GGAAAACCAGAGACC[C/T]TTGTTCACTTGTTTG | 55666 |
rs554160984 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592698 | TCCACAGACACAGTA[A/G]TTAGACTGGGCACAG | 55666 |
rs554165658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624371 | TGCAGTGAGCCAAGA[C/T]GGCGCCATTGCACTC | 55666 |
rs554193788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610112 | TCTTTGAACCACTCA[C/T]TACAGCCAAGTGCGT | 55666 |
rs554227509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586786 | CAAAGAGCTCTACCA[A/G]GCTCTCAGATGGCAC | 55666 |
rs554256341 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625338 | AACCAGACACACTGC[A/T]GTGAAGCCGTCCAGC | 55666 |
rs554346391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619868 | TGGGCAACAGATTGA[G/T]ACTCCGTCTCAAAAA | 55666 |
rs554407033 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564451 | GGCAATAGAGTGAGA[A/C]CCTGTCTCTACAAAA | 55666 |
rs554416573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614440 | CCCTCAGCCACTCCT[C/T]CCACAATGACAAGTA | 55666 |
rs554435910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610546 | TCCCCGAGTATCTGG[A/G]ACTCCAGGTGTACAC | 55666 |
rs554504096 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619605 | GGCGGGGTGCCAGGC[A/G]CAGTGGCTTACATCT | 55666 |
rs554508289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569281 | ATTAGTGTCATCTCT[A/G]AACGAACACTTGGAA | 55666 |
rs554513612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613905 | CTGCATGTGCTGGTT[C/G]CATGTATCTCCACTG | 55666 |
rs554529050 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589942 | GGCTCCTGGTTCATA[A/G]TAACACCAGGGGTGT | 55666 |
rs554552309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618568 | CCCGGCCAGCCGCCC[C/T]GTCCGGGAGGGAGGT | 55666 |
rs554637087 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585667 | CTCCATTTCTGGGGG[C/G]GGGGGGAAAGAAAGA | 55666 |
rs554637147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579945 | CAGCCGCTTATCTAC[C/T]ACTCAGCCAGGCTCA | 55666 |
rs554667100 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574292 | CCCCTCTCTCTTTTT[G/T]GTGTCATGCTATTCT | 55666 |
rs554717274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580523 | CCCTCCCACCTCTAC[A/C]CCAGCAGGCCACCCT | 55666 |
rs554717345 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570936 | ACTTAACTTCCTTTA[-/T]AAAAGAAGAGGAAAG | 55666 |
rs554723933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609217 | TGGAGACGGGGTTTC[A/G]GCATATTGGCCAGGC | 55666 |
rs554760055 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566098 | CAACACTTTCAGAGG[A/C]AGAGGCAGACAGATC | 55666 |
rs554805163 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612066 | TCCAAGTTTGGAAAA[C/T]ACCTACTTCATATGC | 55666 |
rs554843229 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628653 | CTGAAGAGAAACAAC[A/G]CCAGACAGAAATAGT | 55666 |
rs554880319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597417 | GCACTTTGAGAGGCC[A/G]AGGCAGGAGAATCAC | 55666 |
rs554940412 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595259 | GCCAACAAGGCAAAA[C/G]CCAGTCGCTACTAAA | 55666 |
rs554941068 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603046 | TGGTGGTGCACGCCT[A/G]TAGTCCCAGACACTT | 55666 |
rs554965681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590797 | ACCTGACGGCCACAC[A/G]ATCAAAAAAGGTGAG | 55666 |
rs555025171 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595590 | CACCCTGTCACCCAG[A/G]CTGGAGTGCACTGGC | 55666 |
rs555037879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583432 | ACCAGATGCAAAGAG[C/T]AGTTATCATTAAATA | 55666 |
rs555037986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589486 | GAGCTTGCAGTGAGC[C/T]GAGATTGTGCCGCTG | 55666 |
rs555064978 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562501 | CTGAGATCACACTAC[C/T]GCACTCCAGCCTGGG | 55666 |
rs555109232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590194 | CAGGTGCCACTCCAC[A/G]GCCGTGGGCAGACCT | 55666 |
rs555174254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594921 | TGCTCCAGCCTGGGT[A/G]ACAGAGCAAGAACAT | 55666 |
rs555178945 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585674 | TCTGGGGGGGGGGGG[-/A]AAGAAAGAAATCAGA | 55666 |
rs555201872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563109 | GAGACAGAGTCTTGC[C/T]CTGTCGCCCAGGCTG | 55666 |
rs555260018 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578043 | ATTTCAGCCCCACTC[A/G]CTCCTCTAAACTTGC | 55666 |
rs555309893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594497 | AATTTAAAAATTAGG[C/G]CAGGCGCAGTGGCTC | 55666 |
rs555344641 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622062 | GTTGATAAGACCATA[A/G]TGAGTGGTGTGATGA | 55666 |
rs555360420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626548 | ACGACAGCTTCAAAT[A/G]CTCAACAGGACCAGG | 55666 |
rs555398273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627261 | GCCGGGCATGGTGGC[A/G]GGTGCCTGTAGTCCC | 55666 |
rs555424045 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604405 | CTCACTCTCCAATAA[C/T]TCAGAAAATGTTGTG | 55666 |
rs555501153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621006 | CCAGCCTGGGTGACA[C/T]GGTGAGATTCTGTCT | 55666 |
rs555516396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566032 | CTTCCGAGTCAAACT[G/T]CAGGGGATTAATGCA | 55666 |
rs555522103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617620 | CGAGACCATCCTGGC[C/T]AACACGGTGAGATCC | 55666 |
rs555529498 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574420 | CCTCTCCCCCAAGCC[G/T]TCACTCAGATGTTTT | 55666 |
rs555555537 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557406 | AATGATGTGAATGCC[A/G]GAACTTCAGAGTAAG | 55666 |
rs555560501 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576978 | TCGGCAACATAATCC[C/T]AGTTCTAGCAATTCA | 55666 |
rs555594764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576144 | TGAACAGTGGGACTA[C/G]GTCAACCAGGCAAAC | 55666 |
rs555602822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560437 | CAACAGGCCGGGCGC[A/G]GTGGCTCATGCCTGT | 55666 |
rs555622731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622791 | CCTGACCTCAGGTGA[C/T]CCGCCCACCTTGGCC | 55666 |
rs555648551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578132 | CGCCTCCAGACCACC[C/T]CTCCTGACACCTCCA | 55666 |
rs555659810 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621549 | GTGCCCAGATGGTTT[C/T]GATGGGAGCCAGCAC | 55666 |
rs555666690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572225 | ACAGAGTCTTGTGCT[A/G]TCGCCCAGGCTGGAA | 55666 |
rs555674580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638134 | GTGCCACTGTAACTA[C/T]CCAACATATTGTCCC | 55666 |
rs555718794 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572523 | TTCAAATCTTATTGA[A/G]GTGTATGGATAGCAG | 55666 |
rs555748263 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609413 | TCGACCTCAAGTGAT[C/T]CTCTTGCCTCAGCTT | 55666 |
rs555757334 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592266 | GCGCTATGGGGTCCC[C/T]GCATGGCCGTGACCA | 55666 |
rs555784060 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576817 | AAGAAGCACAGAGAG[A/C]GGGGTCCTGGGCCTG | 55666 |
rs555827178 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599147 | TACAAAAATTAACTG[A/G]GCGTTGTGGCGGGTG | 55666 |
rs555828242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582403 | TGTTCTGTGTGTGTA[G/T]GTATGTCTGCATGTT | 55666 |
rs555836020 | snp | A/C/T | 2.17896e-05 | 0.00330065 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604746 | TAGAGTTAACAAGAG[A/C/T]GGGCTGATGAAAACA | 55666 |
rs555870971 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599389 | ATAACAAATTAGGTC[-/A]AAAAAATTGGACCAA | 55666 |
rs555873088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604187 | TGGCCTTCTCCATGG[C/T]TCCTAAGACAGTGAC | 55666 |
rs555878558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616546 | CGATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 55666 |
rs555914144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582912 | GTGAGCCACAGCCAG[C/G]CTCCCGATTCGAAGA | 55666 |
rs555921044 | in-del | -/AAT | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573605 | TGACTAGTCTTAAAA[-/AAT]AATAAAAAATTTTTA | 55666 |
rs555944783 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610834 | GCGGGCGCCTGTAGT[C/G]CCAGCTACTCGGGAG | 55666 |
rs555967545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611868 | GGGAGGCTGAGGCAG[A/G]AGAATGGCGTGAACC | 55666 |
rs556130623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615614 | GAGCTGCTTGTGGGG[A/C]CAAGGCCACTCTCAG | 55666 |
rs556234258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592123 | GAGAGGCGAGGCCTC[C/T]GCATCCCAGCCAGGA | 55666 |
rs556242954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569710 | GGAACACAGGGTTCA[A/G]CTCTTCTCTCTCCCT | 55666 |
rs556251938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597050 | CCCGGGAGGCATTGC[C/T]AGCGGTGAGCAGAGA | 55666 |
rs556274393 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558973 | TAGAGGCGAGAGGTC[G/T]TTCCAACACGGCGGG | 55666 |
rs556292282 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598612 | GAGGATCTGAAACCT[C/G]TGACCCAGCAACCCC | 55666 |
rs556317226 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635271 | TTGAACCCGAGAGGC[A/G]GAGGTTGCAGTAAGC | 55666 |
rs556322850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559837 | TCCCGGGTTCAAGCG[A/G]TTTTCCTGCCTCAGC | 55666 |
rs556403749 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565227 | CAAAGTGCTCCTAGG[A/T]TGCCTGGAGATTAGT | 55666 |
rs556448007 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556537 | TGGCCTTCCTGGGCT[C/T]TGTCCTTCACCTGCT | 55666 |
rs556487887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587505 | TAGTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 55666 |
rs556495451 | in-del | -/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618565 | CCGCCCGGCCAGCCG[-/C]CCCGTCCGGGAGGGA | 55666 |
rs556503811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587008 | TACACAATGAGCAGC[A/C]CACCACACACACTCA | 55666 |
rs556523292 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558899 | CACTGAAAATAAAGA[A/G]AAGGCTGGGTGGTGG | 55666 |
rs556539470 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575261 | CCCGCCACCACGCCC[A/G]GCTAATTTTTTTCTA | 55666 |
rs556584154 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564728 | AGGAGGTGGAGGTTG[A/C]AGTGAGGCAAGATCA | 55666 |
rs556591761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629379 | GTATTTTTAGTAGAC[A/G]GGGTTTCACCATCTT | 55666 |
rs556597758 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573748 | AAATGGTCCAAATAG[A/T]TCCCACTGATGTTTC | 55666 |
rs556600641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581298 | AGGTTGTAGTGAGCC[A/G]AGATTGGGCCACTGC | 55666 |
rs556628797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615194 | AACCTGCATCTCACG[G/T]GTTTAAGCGATTCTC | 55666 |
rs556633206 | in-del | -/TT/TTT | 0.497211 | 0.037236 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628884 | ATCTACAATTCATAC[-/TT/TTT]TTTTTTTTTTTTTTG | 55666 |
rs556646071 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559151 | CCAGCCCCTTGTTCC[C/T]CCAGGGCTGCCCACT | 55666 |
rs556656815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624479 | TGGTGCACGCCTACA[A/G]TCCCAGCTAGTCGGT | 55666 |
rs556740234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619280 | TATTCGGGAGGCTGA[G/T]GCAGGAGAATGGCAT | 55666 |
rs556743021 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579898 | TCCTCTGTGAGCTCA[C/T]CCCCCATTCTCCTCT | 55666 |
rs556744228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580704 | CTGGGGTGGCCCACC[A/T]CCCCTGCTGCAGCAG | 55666 |
rs556776800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581904 | GACCTTCTGGGCAGA[A/G]CTAGTAGCCTCGCTA | 55666 |
rs556786728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574169 | CTCACACATAATTAG[C/T]CCATCTGGAATTCAT | 55666 |
rs556810924 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569222 | CGACTCCTAGCAATT[C/G]TGAGAATGTTCTACA | 55666 |
rs556814858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579191 | CCAGCCTGGCCAACA[C/T]GGCAAAACCCCTCTC | 55666 |
rs556824976 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618506 | GTCAGCGACCCCGCC[C/T]GGCCAGCCGCCCCGT | 55666 |
rs556882325 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615985 | GGTCCATCACACCCC[C/G]CTGTGCCAACAAAAG | 55666 |
rs556897580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618215 | CTAGGAAGTGAGGAG[C/T]GCCTCTTTCCGGCCG | 55666 |
rs556936330 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623521 | ATAAAAAACCCGGCC[A/G]GGCGCGGTGGCTGAC | 55666 |
rs556936782 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603096 | ATTGCTTGAGCCCAA[G/T]AGGGCTGCAATTGAG | 55666 |
rs556944112 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617597 | GGTGGATCACAAGGT[C/G/T]GGGAGATCGAGACCA | 55666 |
rs556950433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584705 | ATAGCAGTTGCTGGA[C/T]ACAAAAATTTACCTG | 55666 |
rs556955953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602541 | AACCCTGTCTCTACT[A/G]AAATTACAAAAATTA | 55666 |
rs556991876 | snp | C/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562668 | ATTATTAAAGAGTTG[C/G]CTGGACATGGTGGCT | 55666 |
rs557041818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605966 | ACTGGGACGACAGGC[A/G]CCCATCACTACGCCC | 55666 |
rs557086762 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613711 | TGTAATTTAATCTCT[C/T]ACAACTTTACCTTAA | 55666 |
rs557125103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577880 | ACTGACATGTGGCCT[A/G]GATTGCCAACACCAC | 55666 |
rs557132033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627775 | CTCTGTCTCAAAAAA[C/T]AAAAACAAAAATTAG | 55666 |
rs557132068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634255 | ATTCACCTGCCTCGG[A/C]CTCTCAAAGTGCTGG | 55666 |
rs557154359 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589627 | ACACCCTGCAGCTCC[A/G]CACACACTTGGCTCC | 55666 |
rs557163075 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608140 | TACCATGAGGATTAG[C/T]GGCTGCAGCCCCTGC | 55666 |
rs557168814 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633929 | TGGAGTGCAGTGGTG[C/G]GATCTCGGCTCACTG | 55666 |
rs557199870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613833 | TCACCCTCTGCTTGG[C/T]CCCCACCTCCCTCAG | 55666 |
rs557202819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596652 | TCCTAACCATTACCA[A/G]TTCCTCATCTAAAAC | 55666 |
rs557243159 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600897 | TGCCACTCCTGCAGA[G/T]ACAATGCTTGGCTTC | 55666 |
rs557250922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594814 | AACTGGGCGTGGTGG[C/T]GCACGCGTGTAGTCC | 55666 |
rs557261498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634945 | CTCAGGACTGTAATC[C/T]TAGCAATTTTGGGAC | 55666 |
rs557269776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562454 | AGAGGCTGGACAATG[C/G]CTTGAACCCGGGAGG | 55666 |
rs557324305 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598168 | GCTTAAAAAGAATGT[C/T]CTCAGTCAGAAACTC | 55666 |
rs557324514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608532 | CCTGGGCAACATAGT[A/G]AGACCCCATCTCTTA | 55666 |
rs557343975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623194 | AGCAAAACTCTGGCC[A/G]GGTGTGGAGGCTCAC | 55666 |
rs557362746 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597168 | AACCAGCGGTGCAAA[C/G]AGACCCTGATAATGC | 55666 |
rs557377946 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81566577 | GAAGAGGCACAGGGT[A/G]CCTGATGTCAAATAC | 55666 |
rs557378049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573096 | AGCTCCAGAAATAAA[C/T]TCATAAGAACCAAAG | 55666 |
rs557437827 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619506 | GGTGAGCTGAGACCA[C/T]GCCACTGCACTCTAG | 55666 |
rs557440967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594032 | TAATCCCAGCACCTT[A/G]GAAGGCCGAGGCGGG | 55666 |
rs557458762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606595 | CTGAAAATCCACCAC[A/G]CATAGTGCTAATAGC | 55666 |
rs557461255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567267 | CCTACACTCTGCCCA[C/T]AGGACAAATGAGGGG | 55666 |
rs557540376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562101 | TAGCCAGGCGTGGGT[A/G]CACGCCTGTAGTCCC | 55666 |
rs557550831 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581141 | GATGACCTGAGGTCA[A/G]GAGTTTGAGACCAGC | 55666 |
rs557670657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633793 | CACTGCAACCTTTGC[C/T]TGCCGAGTTCAAGCA | 55666 |
rs557683476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590130 | AGAAACCTACACGGC[C/T]GCCACACAGAGTTAA | 55666 |
rs557688615 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621840 | TGATTTCCCGGCACA[A/C]AGCTGTGTTCAAGGT | 55666 |
rs557700817 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582973 | CAGGGCCAGGCCTCC[A/T]CCCTGCGGCGCCGCC | 55666 |
rs557705471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599046 | ATAATCCCAGAACTT[C/T]GGGAGACCAAGGCGG | 55666 |
rs557729560 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560401 | CTGGGCGACACAGCG[A/G]GACTCCATCTCAAAA | 55666 |
rs557743679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565961 | TCCTCCCTCACATTT[C/T]ATCCCTCTGCCTCTT | 55666 |
rs557779712 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621768 | AATGACCAACTCTAC[A/G]GGGTGGCATGGGCCA | 55666 |
rs557783742 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632407 | AACCTCTGCCTCCCC[A/G]GTTCAAGTGATTCTC | 55666 |
rs557793797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585719 | GCTCACATCTGTAAT[C/T]CCAGCATCTATAATC | 55666 |
rs557846281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620605 | GTGCTTGCAATGGTG[A/C]CACATAAGGTTCATC | 55666 |
rs557855227 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602637 | AACCCGGAAGGCGGA[A/G]GTTGAAGTGAGTGGA | 55666 |
rs557903012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586863 | GAAGTCTCATCAAAA[C/T]GCAACTCGGCTCTGA | 55666 |
rs557916647 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557359 | CAAATCGCCAATGCT[C/T]TTCCTTTAGCTAAAA | 55666 |
rs557918045 | snp | A/G | 1.6566e-05 | 0.00287797 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622258 | GAAGCCATTATTTTG[A/G]AAGCCAAACTCCTTT | 55666 |
rs557935585 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636472 | GTGACTCATGACAAG[A/G]CACTTGCTGGGAAGC | 55666 |
rs557948686 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588500 | TGAGTAGCTGGGACT[-/C]ACAGTTCATGCCACC | 55666 |
rs557954948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627192 | TCAGGAGATCGAGAC[C/T]ATCCTCACTAACACA | 55666 |
rs557972822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576068 | TAGATTGTAGGTAAG[A/T]GGCACAGAGGACGAT | 55666 |
rs558000435 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557735 | CCGCTTCAACCCAGC[A/T]CCTCTCCACCCTTCC | 55666 |
rs558013947 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558367 | CAGCCTCAGGGCAGG[C/T]GCCACCACTGCTCCT | 55666 |
rs558051477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583332 | TCTGATTTGGCCATA[C/T]AGTCAATAAATGCAC | 55666 |
rs558099097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615045 | TCCTCCTCTTCCTCC[C/T]TAATTTGGGGGTGAT | 55666 |
rs558114582 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557458 | CGGAAACTATAATAG[C/T]GTGGTGGATAAGGAC | 55666 |
rs558133842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614486 | AGCTTCTGCCATCAT[C/G]ACCACCCCCCAAAAA | 55666 |
rs558138881 | snp | C/T | 0.000149399 | 0.00864159 | intron-variant, synonymous-codon | NPLOC4 | GRCh38.p7 | 17:81565407 | GGATGCAGCTGGGTG[C/T]GGAATCCAGGGCACC | 55666 |
rs558150815 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598696 | TGCCTGTGAATTCCT[A/G]CACCAGAAGCCCGTC | 55666 |
rs558194233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582338 | ATGAGGGGCATGGAC[C/T]CGAGTTTCACCTTCA | 55666 |
rs558197898 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604982 | AATAAACATCTGGGC[C/T]GGGCGCAGTGGCTCA | 55666 |
rs558215561 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608104 | TGCCCACCTGGCTGA[-/G]CCTGTGGGCAACTAC | 55666 |
rs558272121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620955 | TTGAGCCCAGAAGGT[C/T]GAGGCTGCAGTGAGC | 55666 |
rs558328418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630152 | CCATGAATGAACTGT[A/G]TTCTTTAAAAAAGAT | 55666 |
rs558328474 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636625 | GGGTGGGGAAGGAGG[A/G]CGGTTTCTCTTCGCC | 55666 |
rs558351803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610824 | GGGCGCGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 55666 |
rs558353267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603185 | TGTCTCAAAAAGAAA[A/G]AGGTTTTAAATTCTA | 55666 |
rs558388430 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616253 | ATGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC | 55666 |
rs558390339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630514 | TCGAGCTCCGGGGCT[C/G]AAGTGATCCTGCCAC | 55666 |
rs558456429 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558671 | AAATCCCACCTGGAC[A/G]TCGGGTGAGAGGAGG | 55666 |
rs558479749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564558 | ACTCTGGGAGGCAGA[A/G]GCAAGCAGATCACAA | 55666 |
rs558501550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601982 | AGGAGGCTAGCCATC[C/T]GGTGATCTCCACAAG | 55666 |
rs558507125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569293 | TCTAAACGAACACTT[A/G]GAAACTCCGCCATCC | 55666 |
rs558519811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611380 | TCTGAGACGGAGTTT[C/T]ACTCTGTCACCCAGG | 55666 |
rs558551599 | in-del | -/AA/AAA | 0.492435 | 0.0610346 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637933 | GTGAGACTTCATCTC[-/AA/AAA]AAAAAAAAAAAAAAA | 55666 |
rs558624395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597029 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 55666 |
rs558654893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569600 | TTCAAGACACAAAGC[A/G]CCCTTCAGCAGCTCA | 55666 |
rs558672159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603993 | GTGGCATAATCATAC[C/T]GAGAGGGCCTTCCAA | 55666 |
rs558712291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564823 | GGAAATGGTATAAAG[G/T]TGTTTGATGTGTCTT | 55666 |
rs558755113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597451 | GTTAAGAGATCGAGA[C/G]CATCCTGGCCAATAC | 55666 |
rs558762825 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591528 | ATTCAAGAAAGAAAA[A/C]TCTAGCAGTTGAGAA | 55666 |
rs558815399 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623525 | AAAACCCGGCCGGGC[A/G]CGGTGGCTGACGCCT | 55666 |
rs558843959 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559522 | GAGCTCCCCGCCCCC[A/C]ACATCCCACCCAGTG | 55666 |
rs558864633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624406 | CTGGGCGACAAGAGT[C/G]AAACTCCGTCTCAAA | 55666 |
rs558885980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592754 | TTTTTGAGGCCGAGA[A/C]AGGCGGATCACTTGA | 55666 |
rs558899285 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629348 | AGGCACCTACCACCA[C/T]GCCCGACTAATTTTT | 55666 |
rs558900079 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597877 | AAGACGGTGGATCAC[C/G]AGGTCAGGAGATCAA | 55666 |
rs558925860 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628104 | GTAGTCCAGCTACTC[G/T]GGAGGCTGAGGCAGG | 55666 |
rs558953633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562683 | GCTGGACATGGTGGC[C/T]TACCACTGCAATCTC | 55666 |
rs558956665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577120 | CCACAGCAAGGGGCA[A/G]TGGGTTCCTCAGAGA | 55666 |
rs558983715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572655 | GGACTCCCCACTGGG[A/G]GAGCACATCAAATGC | 55666 |
rs559002020 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598202 | TTTGTGAGCCAGGTG[A/C]ATCTACATCAACAGG | 55666 |
rs559011901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585702 | AGAGGCTGGGTGCAG[C/T]GGCTCACATCTGTAA | 55666 |
rs559063257 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558862 | CCAGAAAAACATGGG[A/G]GCAGGGAGGCCAAAC | 55666 |
rs559122872 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624137 | TAAAAATACAAAAAT[G/T]AGGCCAGGTGTGGTG | 55666 |
rs559169232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573216 | AAATTATACATCCAT[A/G]ATTTCCAATTATAGG | 55666 |
rs559205533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595097 | GATGGGGACTTGCCA[C/T]GTTGCCCAGGCTGGT | 55666 |
rs559265053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567716 | GCAAAGCAAGCTCTT[A/G]CTCTCTTCTCCCAAG | 55666 |
rs559269370 | snp | A/G | 2.25522e-05 | 0.00335792 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600434 | TGTACCAATCTGCAG[A/G]GAATCAAAGGGAGAA | 55666 |
rs559287431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612914 | ACCTCACATGGATGC[A/G]CACACACAACCACCT | 55666 |
rs559348313 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566092 | TAATCCCAACACTTT[C/T]AGAGGCAGAGGCAGA | 55666 |
rs559372534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617038 | ATCTACAGCAATGCA[A/G]GGGGCAGGGATACAA | 55666 |
rs559378121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560156 | GGTGCAGTGGGTCAC[A/G]CCTGTAATCCCAGCA | 55666 |
rs559384479 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638256 | TTACTACTCAAAAAA[A/C]ATTAGTGTCCTTGAG | 55666 |
rs559400026 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590972 | AGGAGGCAGCCAACC[C/T]TGCACAAATGACCAC | 55666 |
rs559481602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561699 | GGATCCTCCCATTTC[A/G]GCCTCCCCAGAAGCT | 55666 |
rs559504048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606248 | CGGCAGGAGGAAGGC[A/G]AGGCAGGCTACTCAG | 55666 |
rs559544492 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566174 | CCGTCTCTACTAAAA[A/G]TACAACAATTAGACA | 55666 |
rs559563331 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560488 | CTGAGGTGGGCAGAT[A/C/G]ACAAATTCAAGAGAT | 55666 |
rs559564683 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81556912 | CGCTTTTATTAGGTT[C/T]CACTGCAGGGCTGGG | 55666 |
rs559658627 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634000 | TCCTGAGTGGCTGGG[A/G]CTACAGGTGCACGCC | 55666 |
rs559700567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610879 | ATGGCGTGAACCCGG[A/G]AAGCGGAGCTTGCAG | 55666 |
rs559707980 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559723 | GCATTTGGGTTGTTT[C/G]CAGCTTTTTTTTTTT | 55666 |
rs559726836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571308 | CTCCGGTGGGGCTGA[C/T]GCACTGGCTTCTGCA | 55666 |
rs559747279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627340 | GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 55666 |
rs559820284 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81610215 | AGACTCTCACCTCTA[A/G]AGGGACGCAGTGCAC | 55666 |
rs559866727 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592434 | AGTCTGAGCACCAAG[A/C]GGGGTGATTCACACA | 55666 |
rs559868083 | snp | C/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637596 | CTGAGGTCAAAAGTT[C/T]GAGACCAGCCTGGCC | 55666 |
rs559872781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599160 | TGGGCGTTGTGGCGG[C/G]TGCCTGTAATCCCAG | 55666 |
rs559934242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598776 | CTCGGGAAGGATCTG[C/T]GGCCCATGACCCTCT | 55666 |
rs559935119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620700 | AGGGAGAAAAAAAGG[C/G]CAAGCAACAGAAGAG | 55666 |
rs559958887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594131 | ACAAAAAAAATTAGC[C/T]GGGCATGGTAGCGGG | 55666 |
rs559971869 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588886 | CAAATTAGAAAGGTC[A/C]AAGACAGGTTCACAC | 55666 |
rs560001584 | snp | A/G | | | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81564173 | TAGTACCTGGGTGAT[A/G]TGATCAATCATACCC | 55666 |
rs560004509 | snp | A/G | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81639036 | AACTAAGCGCCTCCC[A/G]AAGTTATTTCAGCCT | 55666 |
rs560069384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616035 | AAAAGCTGCTAAATC[C/T]GGGCCGGGCGTGGTG | 55666 |
rs560081025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580109 | CTCCACCTCATTCCC[C/T]CAAGGTGGGGTTCTC | 55666 |
rs560144360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625572 | CAGCAGAAGGGAGAG[A/G]GCAGAAGAGTCAACC | 55666 |
rs560146776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570916 | AAAACTGCACTAAGG[C/G]AAAAACTTAACTTCC | 55666 |
rs560174901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559657 | TTGCTGGTTCCTTTT[C/T]GTTGCAGAGGGTGCT | 55666 |
rs560192245 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587072 | TCCACGGAAAACACA[C/T]TGCAGCTGCAGACCC | 55666 |
rs560204747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592879 | ATCCCAGCTACTTGG[C/G]AGACTGAGGCACAAG | 55666 |
rs560216917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580880 | AAACACAACAGCTCT[C/T]GCTCCCCGCTCAGCT | 55666 |
rs560218069 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636723 | AGTCCCCTGGGGAGG[A/G]ACACGGACGGGAAGC | 55666 |
rs560229703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610323 | TTCCGCTGCTGCTGT[C/T]TCACATGCACGTCCT | 55666 |
rs560341832 | in-del | -/AC/CC | 0.292827 | 0.246304 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574879 | ACAAACAAACAAACA[-/AC/CC]CACACACACACACAC | 55666 |
rs560374640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575071 | CGCCACAGGATAACT[C/T]AGAAAAAACAAAGCT | 55666 |
rs560400294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597517 | AGGCCGGGTGCGGTG[A/G]CTCACGCCTGTAATC | 55666 |
rs560423504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582184 | CAAGCTGAGGCCCAG[C/T]GGTTGTCCTGCAGGC | 55666 |
rs560439388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603634 | AAAATTTCTAACATA[C/T]AGCTAATTTAAAGAA | 55666 |
rs560463463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576280 | GTAGGTAGATGCATA[A/G]TTCTGGGGGAAAGAA | 55666 |
rs560471073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582462 | GCTGGAGTACAGTGG[C/T]ACAATCATAGCTCAC | 55666 |
rs560484159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619353 | CTGGACTCTAGCCTG[A/G]GCAACACAGTGAGAC | 55666 |
rs560493722 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624537 | CTGGGAGGCGGAGCT[G/T]CAGTGAGATGAGATC | 55666 |
rs560522783 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608898 | GCCTCTGCTACGCAC[A/T]GGGGGAGGCCAGCAG | 55666 |
rs560552778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569403 | TCCCCTCGTGGCACA[C/G]CTTCCCTTCAGAGTC | 55666 |
rs560589002 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636304 | TAAAAAGTGAAATCA[A/G]CATCATTTACAACAT | 55666 |
rs560594429 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616590 | AAAAAATTAGCCGGG[C/T]ATGGTGGCAGGTGCC | 55666 |
rs560721918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613587 | AAAAGCAAATGCCAA[A/C]CACCCCTGTAGGCCT | 55666 |
rs560737225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615256 | AGACATGTGCCACCA[C/T]GCCCAGATACTTTTT | 55666 |
rs560775434 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595736 | TTATAAAGAGATGGG[A/G]TTTCGCTATGTTGGC | 55666 |
rs560784702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81564214 | ATCAGGCAATATACC[C/T]AGGTGACAAACCTGC | 55666 |
rs560789351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563310 | AATCCCTTGACGTTG[A/T]GATCCACCTGCCTCA | 55666 |
rs560818907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624011 | GGTTTCTGGCCGGGC[A/G]TGGTGGCTCATGTCT | 55666 |
rs560826963 | in-del | -/A | 0.436692 | 0.166271 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619202 | CAAGAATGATCAATT[-/A]AAAAAAAAAAAAAAA | 55666 |
rs560830220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607578 | TTTTGGTGGTGAGCC[A/G]TTTTTGGTATCATAG | 55666 |
rs560886573 | in-del | -/AAC | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613133 | TAAAAAGCTAAAAAA[-/AAC]AAAAAACAAAAACCG | 55666 |
rs560893182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596735 | TGAGCCCTGAAAATC[A/T]CTGCTTTATAAAGGT | 55666 |
rs560900472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600325 | CCCCCTGCTTGGCTG[C/T]CGGATGCCTCAGTAC | 55666 |
rs560909202 | in-del | -/TTTC/TTTTT | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615096 | CATCAGAGACGTCTG[-/TTTC/TTTTT]TTTCTTTTTTTTTTT | 55666 |
rs560939467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627484 | GTGGCTCACGCCTGT[A/G]ACCCCAGCACTTTGG | 55666 |
rs560952233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635008 | CCAGCCTGTACAACA[C/T]AGTAGAGACCTCATC | 55666 |
rs560955008 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625374 | GGTGGGCGCATCTGT[A/G]TCTGAGCCCAGGCAA | 55666 |
rs560991570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608246 | AGATTCTCACAGGGT[A/G]GTTGTTTTTCTGAAA | 55666 |
rs560991831 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606878 | CAAGAGGCTGGAAAT[C/G]ACATGCTAAGTATCT | 55666 |
rs560992338 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568717 | AGGGGCCAGGCCAAA[C/G]CAACAGTGACGAGGC | 55666 |
rs561002203 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634628 | TCTTGCTCTGTCGCC[C/T]AGGCTGGAGTGCAGT | 55666 |
rs561003189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627849 | GCTGAGGCAGGAGAA[C/T]TGCTGGAACCCAGGA | 55666 |
rs561024757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595929 | GTTTTGGGGTTTGTG[G/T]TTATATAGTTTTATG | 55666 |
rs561089694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601569 | GCCTCAATTATACTT[C/T]TAATAGAACCGTTGA | 55666 |
rs561117632 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624273 | AAATACAAAAATTAG[C/G]TAGGCGTGGTGGCGG | 55666 |
rs561130827 | in-del | -/AA/AAA | 0.434831 | 0.168337 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635357 | AAATAAAATAAGGTT[-/AA/AAA]AAAAAAAAAAAAAAA | 55666 |
rs561135452 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588629 | CTGGGATTACAGGCA[C/T]GAGCCACCATGCCAA | 55666 |
rs561198141 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558267 | CGCCCTCAGCCAGGC[A/G]GTGCAGTGGGACGAA | 55666 |
rs561263453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595025 | AAAAACTTCGCAGTC[A/G]GCTTGAACACTTTTC | 55666 |
rs561286428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594724 | AACCTGCAGGGAGCC[A/G]AGATCGCGCCACTGC | 55666 |
rs561305552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561547 | TAAAAGAATCTTTGC[C/G]TACCCCAAGGCCCTG | 55666 |
rs561367983 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601232 | TCTCAAATTGAGTTA[C/T]AGTAACTGGGCATAT | 55666 |
rs561448311 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582994 | CGGCGCCGCCCCTGC[A/G]CACTCACAACTGAGC | 55666 |
rs561466161 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618266 | GGAGCGTCTCTGCCC[G/T]GCCGCCCATCGTCTG | 55666 |
rs561472615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589218 | CCTCAAGAGTTTGTC[A/G]GGGGTAAGAGTTAAA | 55666 |
rs561509489 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617808 | CGATTGCAGGCGCGC[A/G]CCGCCACGCCTGACT | 55666 |
rs561532747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605640 | GCTACGGAGTGAGAC[A/T]CTGTCTCAAAAAAAA | 55666 |
rs561573116 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578407 | GAGGGACCTGCTCAC[C/T]GTGGCGCCCCAGGCC | 55666 |
rs561619284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573385 | TGTCTTCTGAGACAA[C/T]CATCACAAGCTGTTC | 55666 |
rs561634958 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576475 | GGGGCGTGAGTGCAT[A/G]TGGACTTGACTATAT | 55666 |
rs561635435 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598669 | GTGCTGTGTGATCCT[C/T]AGGCCCGCCTCTGCC | 55666 |
rs561663648 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613170 | AGCTAACAAGATAAC[C/T]TGAAGTTTAATCTGA | 55666 |
rs561696429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606080 | GCCCACCTCAACCTC[C/T]CAAAGTGCTGGGATT | 55666 |
rs561756695 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616985 | CCCAAATCTCCCTCC[G/T]GCAGGCAGCTAGACC | 55666 |
rs561758544 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557742 | AACCCAGCTCCTCTC[C/T]ACCCTTCCTGACCCT | 55666 |
rs561758684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577545 | CCTCTGAACCACGGC[G/T]TGGCTCATCTACTTC | 55666 |
rs561774016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570118 | GTGCCAGCGCCAGCC[A/G]CTGTGGAAGGACAGC | 55666 |
rs561860029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616661 | GGTGAACCCAGGGGG[C/T]GGAGCTTGCAGTGAG | 55666 |
rs561884131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615620 | CTTGTGGGGCCAAGG[A/C]CACTCTCAGTAATTC | 55666 |
rs561899897 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629482 | TGTGAGCCACCACGC[C/G]CAGCCGTGAAATATT | 55666 |
rs561916405 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81566620 | TTTTGAGACAAAATA[C/T]AGACACAAAATAAAC | 55666 |
rs561921142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611720 | AATCCCAGCACTTTG[A/G]GAGGCCGAGGCGGGT | 55666 |
rs561945260 | snp | A/G | 3.9744e-05 | 0.00445763 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572091 | ACTTGTCTACGTCCT[A/G]CAATAGTCAGAGGGG | 55666 |
rs561978182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566263 | CTTGAACCCAGAAGG[C/T]GGAGGTTGCAGTAAG | 55666 |
rs562020555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587884 | GTTTCACCGTGTTAG[C/T]CAAGATGGTCTCAAT | 55666 |
rs562049733 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609568 | TCTGGCCCTGGCCTC[C/G]CAAAGTGTCGGGACT | 55666 |
rs562089363 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609890 | AATCAACAATGATAA[C/G]CACGGAGGCCGACAG | 55666 |
rs562125597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627935 | AAAAAGACTCCATCT[C/T]AAAAAAAGAAATTTG | 55666 |
rs562135345 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629587 | GCAATCCAACCCAAC[G/T]GTGATAGAGAAAGGC | 55666 |
rs562139215 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575755 | TTGAAGTTGAGGCTC[A/G]GACCCCAACAGCCGT | 55666 |
rs562159037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598319 | TTAGAGATGAGTTTC[C/T]TCAGCACCAGCTCTG | 55666 |
rs562192160 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559715 | GGGGATGTGCATTTG[C/G]GTTGTTTCCAGCTTT | 55666 |
rs562212043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604424 | GAAAATGTTGTGCAC[A/G]TGCACCGGTGTGTGA | 55666 |
rs562215338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630287 | GAAATTTTCTAATTG[C/T]TACTTTTTTTTTGCT | 55666 |
rs562277000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604989 | ATCTGGGCTGGGCGC[A/G]GTGGCTCACGCCTGT | 55666 |
rs562298488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597181 | AAGAGACCCTGATAA[C/T]GCAGGCCAACACCAT | 55666 |
rs562299212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631810 | TTAGCTCATTTTTTT[C/T]TTCCCCGAGATGAAG | 55666 |
rs562323236 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626300 | CAGCCTGGGCAACAG[A/G]GCGAGACTCCATCTC | 55666 |
rs562359187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602918 | ATACATATATATGTA[C/T]ATATACACACACACA | 55666 |
rs562411320 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582210 | CAGGCTGCAGCAGCA[C/G]AACCAGGAGGGCCGT | 55666 |
rs562444482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593532 | GTGTCGGCAGCCTAC[A/G]TTAACTATGTTACCC | 55666 |
rs562472553 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604492 | CCTCTCCGAAAGGGC[A/G]TCCCCCACAGCCTCC | 55666 |
rs562509767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591011 | CAGCAAAGATACAGG[C/T]ACCTCACTTGCCCAT | 55666 |
rs562539429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620271 | GGAAGGCCAAGGCGG[A/G]TGGATCACGAGGTCA | 55666 |
rs562586560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637671 | ATACGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55666 |
rs562610342 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636214 | GACCCCAGGTGATCC[A/T]CCCGCCTCGGCCTCC | 55666 |
rs562611981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591932 | GACTATGAGGACACA[C/G]ATGCCCAGCCCAGTG | 55666 |
rs562640846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586470 | CAAAAAATTAGCCGG[A/G]CAGGTGGCACACATC | 55666 |
rs562645155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597510 | AGAAATTAGGCCGGG[C/T]GCGGTGGCTCACGCC | 55666 |
rs562647554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585294 | CCGACGACAGAGAAG[A/C]ATCAAAGATTAAAAG | 55666 |
rs562693315 | snp | G/T | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635575 | CATTCTGTCGCCCAG[G/T]GTGGAGTCCAGTGAC | 55666 |
rs562727639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614541 | GTTTTCCTTCTAAAG[A/G]GCAAACTCCCAGGAG | 55666 |
rs562754388 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630336 | GCTGTCACCCAGGCT[G/T]GAGTGCAGTGGCAAA | 55666 |
rs562765574 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613945 | CGTTCACATACACAC[A/G]TAAGCACAGACACGC | 55666 |
rs562779341 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626993 | TACTCGGGAGGCTGA[A/G]GCAACAGAATCACTT | 55666 |
rs562799311 | in-del | -/A | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558877 | GCAGGGAGGCCAAAC[-/A]AAAAAGCACTGAAAA | 55666 |
rs562825729 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616758 | AGAGTAACACACTAC[C/T]ACGCAAGTAAGAGTG | 55666 |
rs562897873 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618425 | CCTCCGCCCCGCAGC[C/T]GCCCCGTCTGGGAAG | 55666 |
rs562902357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628965 | CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACA | 55666 |
rs562936003 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579791 | ACTTCTCAATCCCAC[C/T]TCCCATACTGGTGAC | 55666 |
rs562997802 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559834 | ACCTCCCGGGTTCAA[A/G]CGGTTTTCCTGCCTC | 55666 |
rs563223141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590384 | CCCTGAAGTGAGCTG[G/T]GCAGATGATGCCATG | 55666 |
rs563224452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602312 | AGTACTTTAGGAGGC[C/G]AAGGCAGTAGGATCA | 55666 |
rs563257000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612982 | ACACCCCACTCTGCA[C/T]GGGAATCAGCATCTC | 55666 |
rs563293733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601144 | ATGTTCACTTAAATG[C/T]AGCTTGCGGGTCATT | 55666 |
rs563296516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612415 | AGATCATGCAAGCAA[A/G]CCAGTGCCAGGCCCC | 55666 |
rs563366425 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610039 | CATAAATAAAGGCTC[A/G]TCCTGTGTGCAGCTT | 55666 |
rs563367293 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568761 | CACAAAGCAACACAT[C/T]TGGGAAAATTACGAG | 55666 |
rs563411514 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633556 | GCCTCTGACACAGAC[C/T]ACAAAATGAAATACA | 55666 |
rs563411551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627015 | GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC | 55666 |
rs563420380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606908 | TTATACCTCCTGAAC[A/G]GTGTCTCAGGAGCTA | 55666 |
rs563451655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595184 | TACAGATGTTGTAAT[C/G]CCAGCACTTTGAGAG | 55666 |
rs563481666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607425 | GAAATCTGTATCTTT[A/G]AGGTAGACGTGAGGT | 55666 |
rs563505920 | in-del | -/A | 0.249603 | 0.25 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590671 | TTATAGTTTTGGATG[-/A]AAAAAAAACCCTCAA | 55666 |
rs563519694 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634068 | GTAGACGTGGGGTTT[C/T]ACCGTGTTGCCCAGG | 55666 |
rs563572497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627385 | CAACAGAAAGACTCC[A/G]TCTCAAAAAAAAAAA | 55666 |
rs563604661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561261 | CATGCCCGACCTGCA[C/T]TTCCTTTTGTGAAAC | 55666 |
rs563639363 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638967 | GTCCCCAGGTAGGAA[A/G]GGAGTTTGTTTTGCA | 55666 |
rs563675732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599767 | TCAATAGAATAAAAA[A/T]GGAAATCCTTTTCTC | 55666 |
rs563677983 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594003 | ACTCGGCCGGGCGCA[A/G]TGGCTCACGCCTGTA | 55666 |
rs563707686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593441 | TAAACGTATGACTTT[A/G]TTCTGTTTCTTTCCT | 55666 |
rs563708137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605428 | AGGCAGGCGGATCTC[C/T]TGAGTCCAGGAGTTA | 55666 |
rs563719460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566217 | GGCACCTGTAATCCC[A/C]GCTACTCGGGAGGCT | 55666 |
rs563733145 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557879 | GAGGTGTCAGCCATG[G/T]CCCTGACCACTTCAG | 55666 |
rs563748955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638360 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 55666 |
rs563750215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588729 | CTCAAAGCCAGTGCA[C/T]GTAGCTCCACTTCTG | 55666 |
rs563758333 | in-del | -/T | 0.497776 | 0.0332724 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633872 | ACCGCGCCCAGCTAA[-/T]TTTTTTTTTTTTTTT | 55666 |
rs563786166 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622957 | CCCAGCACTTTGGGA[G/T]GATGAGGTGGGAGTA | 55666 |
rs563815816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594192 | AGGCAGGAAAATGGC[A/G]TGAACCCGGGAGGTG | 55666 |
rs563848039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587770 | GCCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC | 55666 |
rs563897542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587151 | TGCAGAAATAAGCAG[A/G]TGATATGAGTTAGTA | 55666 |
rs563916392 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609168 | AGGACTACAGGTGCA[A/C/T]GCCACCACGCCCAGC | 55666 |
rs563924026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616619 | CCTGTAGTCCCAGCT[A/G]CTCGGGAGGCTGAGG | 55666 |
rs563947767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601983 | GGAGGCTAGCCATCC[A/G]GTGATCTCCACAAGA | 55666 |
rs564012136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583575 | TGGCCCTAGTCCCTC[A/G]GGAAGCTCCTGGTCC | 55666 |
rs564084143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611698 | GGTGTGGTGGCTTGC[A/G]CCCTGTAATCCCAGC | 55666 |
rs564090250 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583910 | TGGTATTATACTCTA[G/T]GTATAGATGCATTTT | 55666 |
rs564107798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626230 | CTGAGCCAGGAAAAC[C/T]GCTTGAACCCCGGAG | 55666 |
rs564176390 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575116 | TACTTTTCTTTTTTT[C/T]TGAGAGGGAGTCTCG | 55666 |
rs564187825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565762 | TGCAAACTGCCACAA[C/T]TTACATCTATAAACG | 55666 |
rs564203451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582520 | GATCCTTCTGACTCA[A/G]CCTCCTGAGTAGCTG | 55666 |
rs564220329 | snp | C/T | 0.000612679 | 0.0174918 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613377 | GAGGTACTGATCAAT[C/T]TCATCCTCCACCACG | 55666 |
rs564264510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575356 | TCCACCCGCCTTGGC[C/T]TCCCAAAGTGCTGGG | 55666 |
rs564282987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625314 | TTTGACACTGAGATC[A/G]GAGGTGACAACCAGA | 55666 |
rs564335502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571909 | CTGCTCAAGGCAGAG[A/G]GTGCCTTAAATTGCA | 55666 |
rs564421652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592947 | AAGATTGTGCCATGG[A/C]ACTCCAGCCTGGGTG | 55666 |
rs564457127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615359 | CCTGCCTCGGCCTCC[C/T]AAAGTGCTAGGATTA | 55666 |
rs564491067 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614727 | TGGCATGGCAAACTG[C/T]TGACCTCAGAGGCTA | 55666 |
rs564493216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620145 | AAGAAGTAAGACATA[A/C]AAATTTCCTTAAAAA | 55666 |
rs564497344 | in-del | -/A | 0.00119737 | 0.0244387 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556796 | ACGTAAAACAGTGAT[-/A]ATCTTGGAGACAAGT | 55666 |
rs564612674 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635384 | AAAAAAAGGAGTCGA[C/T]GTTTCCTAAGTTTCT | 55666 |
rs564625900 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631704 | GACAGGAACATGCGC[A/G]TAAGTGTCCTAGCTT | 55666 |
rs564674950 | snp | A/C/G | 7.93053e-05 | 0.00629654 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610173 | CTACCCGCAGCCCCC[A/C/G]ACACTGGCCCAGAAC | 55666 |
rs564686275 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564987 | CAGCAATGCTGACAG[A/T]AGGTTCTCACGAGTG | 55666 |
rs564710006 | snp | A/G | 0 | 0 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563351 | GTGCTGGGATTACAG[A/G]TGTGAGCCAGCCACC | 55666 |
rs564732406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608312 | CCACCATCACAGATG[C/T]TAACTTGCTGGGGTG | 55666 |
rs564743117 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559018 | GATTAGGCGTGAGGA[A/G]CCGCTCTGCGTTTCC | 55666 |
rs564774479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568854 | TAGCCATGGGAAGGG[C/T]GTCCACGTGACCAGC | 55666 |
rs564781017 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636746 | CGGGAAGCAGCCGAG[C/G]GGGGTGAAAGTCCCC | 55666 |
rs564850357 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623933 | TCAACAAATATTAAG[C/T]AGTTCTATGTGCTCA | 55666 |
rs564891848 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604986 | AACATCTGGGCTGGG[C/G/T]GCAGTGGCTCACGCC | 55666 |
rs564908903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595747 | TGGGGTTTCGCTATG[C/T]TGGCCAGGCTGATCT | 55666 |
rs564930730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624576 | ACACTCTAGCCTGGG[C/T]AACGGAACAAGACTC | 55666 |
rs564954003 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620525 | ATAAAAAAATGCAAA[-/C]CCGGTGATTACTGTT | 55666 |
rs564957756 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597107 | AAAAGAGCAAGACTC[A/C]GTCTCAAAAAATACA | 55666 |
rs564963140 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564038 | GTGAGCTAAGATTGC[A/C/G]CCACTGCACTCCAGC | 55666 |
rs564967160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629040 | CCCGCCACCACACCC[A/G]GCTAATTTTTTGTAT | 55666 |
rs564968106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629514 | TTACACTTACCTTTG[A/G]GCTCTTGGTCCTATA | 55666 |
rs565036403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602739 | ATCAAACTTCAGGAA[G/T]TCCAACTAAAAAGAT | 55666 |
rs565052405 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625028 | GGAAGCTAGAGTGCC[A/C]ATTAGAGACAAGAGA | 55666 |
rs565125041 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628285 | TGGCTCACACTGAAG[C/T]GGGTGGATCACGAGG | 55666 |
rs565136644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619406 | AAAACAAAATTAGCC[A/G]GGCGTGGTGGCACAT | 55666 |
rs565154527 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618354 | CCTGGCCGCGACCCC[A/G]TCTGGGAGGTGAGGA | 55666 |
rs565182014 | in-del | -/TCTC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606199 | AGGAGGCCACGGAAT[-/TCTC]TCTAAGGAGCCGTTT | 55666 |
rs565193439 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590716 | TTTCTTTGACAAAAA[C/G]AATCACTTATGATCA | 55666 |
rs565230901 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599447 | ATTTGAACCCAAATA[C/T]GCCCCTAAATCAAGA | 55666 |
rs565234716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584963 | CCTGCTGAGCTCAGG[A/C]GTTCATGACCAGCCT | 55666 |
rs565246964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590228 | AGCCCAGCTCCTCCA[C/T]GGTTTCACCCTCCAC | 55666 |
rs565279256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623193 | GAGCAAAACTCTGGC[C/T]GGGTGTGGAGGCTCA | 55666 |
rs565285612 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558291 | GGACGAAGCAGCGTA[C/T]TGGGGAGGGCCAGAG | 55666 |
rs565315590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627873 | CCCAGGAGGCGGAGG[C/T]TGCACTGAGCCGAGA | 55666 |
rs565411260 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601072 | TGGCTCCCATGCAAC[G/T]GAAACCAACCACAGC | 55666 |
rs565420282 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619561 | TCTCAAGAAAAAAAA[-/G]AAAAAAAGAAAGAAA | 55666 |
rs565469924 | snp | A/C | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561571 | GGCCCTGAAGAGATT[A/C]AACTTAATAACTGTT | 55666 |
rs565494220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594343 | AAATAGTTAACATGT[A/G]TTAATTATTAACATA | 55666 |
rs565509962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579353 | ATTGCACATCACCCT[A/G]GGTGACAGAGCGAGA | 55666 |
rs565519717 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611737 | AGGCCGAGGCGGGTG[C/G]ATCACAAGTCAGGAG | 55666 |
rs565534125 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574436 | TCACTCAGATGTTTT[C/T]GCCAGCCAATCCCTA | 55666 |
rs565558030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599376 | TGAACTGTAAGATTA[C/T]AACAAATTAGGTCAA | 55666 |
rs565579116 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589403 | GTGCGGTGGCGGGCG[C/T]CTGTAGTCCCAGCTA | 55666 |
rs565656249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572179 | ACCTTTTATTTAATT[A/T]ATTAATTTATTTATT | 55666 |
rs565684367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594838 | GTAGTCCCAACTACA[C/T]AGGAGGCTGTTGGGG | 55666 |
rs565718336 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566740 | TTCTGAGTCAGTGGC[A/G]GAGCAGCTCAGAAAG | 55666 |
rs565778782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559493 | TGGGCATGGGGGCAG[A/G]GGCAGGCAGCTGAGA | 55666 |
rs565784824 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637122 | CAATACGCTCCCCTC[C/G]GGCGCGAGGCCGGGA | 55666 |
rs565788325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565917 | GAGGCTGGGATGGAG[A/G]GCGGAAGTCTTGACT | 55666 |
rs565803634 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637895 | ACTGAGTTGGTGCCA[C/T]TGCACTCCAGTCTGG | 55666 |
rs565804962 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556431 | GCACTTGTTCTAGAC[A/G]CTTTCTGTTGTCACA | 55666 |
rs565810203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627532 | ATCACCTGAGGTCAG[A/G]AGTTCGAGACCAGCC | 55666 |
rs565818362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589262 | TCGGCCGGGTGCGGT[A/G]GCTCATGCCTGTAAT | 55666 |
rs565894479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592712 | AATTAGACTGGGCAC[A/T]GTGGCTCACACCTGT | 55666 |
rs565916194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632995 | ATTAGCCAGGCGTGG[C/T]GGAGGGCGCCTGTAG | 55666 |
rs565947281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583193 | AAAAACCTTCCTCCC[C/G]AGCAATTCTATTTTG | 55666 |
rs565981671 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625886 | GGGCGCGGAGGTTCA[A/T]GCCTGTAATCCCAAC | 55666 |
rs565985111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565114 | GGCTTCTCCTCCTTA[C/T]AGCTTTAAGCACTAA | 55666 |
rs565987143 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630506 | GGCTGATCTCGAGCT[A/C]CGGGGCTCAAGTGAT | 55666 |
rs565990205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633720 | AACTCTTTTCTCCCC[C/G]CAAGACAGAGTCTTG | 55666 |
rs565992376 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630376 | TACTGCAGCCTTGAC[A/T]TCCAAGGTTCAAGTG | 55666 |
rs566011022 | in-del | -/A | 0.0475351 | 0.146656 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587631 | ACACCCTGTCTCTTT[-/A]AAAAAAAAAAAAAAA | 55666 |
rs566011198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588798 | ATCCAGCCCCAGAAA[C/T]GTGACAGAAGCCTTT | 55666 |
rs566027013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576687 | AAAGGGTTAATATAC[A/G]AAGACCTCACAAATG | 55666 |
rs566038278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598457 | AATAAACATTTCAGA[A/G]AGTAGGTCTTTCCTG | 55666 |
rs566083221 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604485 | GGCAAGGCCTCTCCG[A/C]AAGGGCGTCCCCCAC | 55666 |
rs566091881 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605598 | GGTTGCAGTGAGCCA[A/C]GACTGCACCACTGCA | 55666 |
rs566099636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597833 | GGGTGTGGTGGCTCA[C/T]GCCTGTAATTCCAAC | 55666 |
rs566114500 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587956 | CTGGGATTACAGGCA[C/G/T]GAGCCGCCGCGCCCG | 55666 |
rs566122608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619660 | GAGGCGGGTGAATCA[C/G]TTGAGGTCAAGAGAT | 55666 |
rs566170101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626387 | GAAAACCCCAAAATT[G/T]AATGAAAAACATCAA | 55666 |
rs566183508 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602207 | ATCTCGCTCAGGAGC[A/G]AGACCTTGTTTCAAA | 55666 |
rs566185878 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620304 | AATTCGAGACCAGCT[A/T]GGCCAACTTAGTGAA | 55666 |
rs566209667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593109 | GCCCGCTACACACTT[C/G]TGTAGGCAAAAACCA | 55666 |
rs566268478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621445 | CACCACTGAGCCAGT[A/G]GCCACAGCACATGCA | 55666 |
rs566272690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616178 | AAAAAAAAATTAGCC[A/G]GGGGTGGTGGCGGGC | 55666 |
rs566282485 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619233 | ACACAAAAAATTAGC[C/T]GGGCATGTTGGCGGG | 55666 |
rs566330234 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616487 | TGTAATCCCAGCACG[C/G/T]TGGGAGGCCGAGGCA | 55666 |
rs566398833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614960 | AAGGAAGAGCAGAGG[C/T]CAAAGTGCAGGCCCT | 55666 |
rs566416770 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636528 | GGGAGATTAGGATAA[A/G]AGGTGTCCCTGGCTC | 55666 |
rs566436915 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586082 | TTGAGATCAGGAGTT[C/T]GAGACCAGCCTGCCC | 55666 |
rs566562860 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620382 | GAGCCTATAGTCCCA[C/G]CTACTCAGGAGGCTG | 55666 |
rs566566654 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575191 | TGCAAGCTCCGCCTC[A/C]CGGGTTCAAGCCATT | 55666 |
rs566584055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569561 | GTCATTGGATTCGGA[A/G]GGCAAATGAGCAATC | 55666 |
rs566621757 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632478 | CCACCACGCCTGGCT[A/G]ATTTTTAGTATTTTT | 55666 |
rs566637705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609926 | GCTTTGTGTCAGATC[A/G]GAAAAGGATTGTCCA | 55666 |
rs566658946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601582 | TTTTAATAGAACCGT[A/T]GAGCTCTCCATGAAA | 55666 |
rs566677814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615537 | TCTAAAGAAAGTAGA[C/G]GAAATCCCCAGGGGA | 55666 |
rs566685143 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596989 | ATGGTGGCAGGCGCC[G/T]GTAGTCCCAGCTTCT | 55666 |
rs566707477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575495 | CTGGCATTTCTCAGG[C/G]GCCAGCTGTGTGCAC | 55666 |
rs566721014 | snp | A/G | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556617 | AGGGCTGACAGGTGC[A/G]GCAGAGGCAGAAGAG | 55666 |
rs566730869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608031 | GGCAAGGGCTTGCCA[C/T]GGCTTAAAAGAAATC | 55666 |
rs566760155 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574210 | AATTAAGCTCTAATA[C/T]GCAGAAACATTTTTC | 55666 |
rs566778231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570186 | TCATGGGCAAGCGGC[A/G]GGGTGGGTCATGAAG | 55666 |
rs566786374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574066 | TCTCAATGGAGATTT[G/T]GTAGGAGGCAAAAAT | 55666 |
rs566839651 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614947 | AACCAACACGGTGAA[A/G]GAAGAGCAGAGGCCA | 55666 |
rs566927943 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563151 | CACGATCTCAGCTCA[C/T]TACAACCTACGCTTC | 55666 |
rs566942612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634834 | GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC | 55666 |
rs566948807 | snp | C/G/T | 1.68903e-05 | 0.00290601 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569133 | AAGAAAAACACAAAC[C/G/T]CATGATAAATGAGGC | 55666 |
rs566953803 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561980 | TATACACGTCTGTAA[G/T]CCCAGCACTTTGGGA | 55666 |
rs566960885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574564 | GCAGCCGTCAAAGTG[G/T]CAGCAGCTTTATCTC | 55666 |
rs566994825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608419 | GCTAGCTCCCTTCTA[C/G]AACCAGGTTGGCCAG | 55666 |
rs567038858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562304 | AGCACTTTGGGAAGC[C/T]GAGGTGGGTGGATCA | 55666 |
rs567099734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591368 | TGACCCCAGGTAGCA[A/G]AGGCTGCGATGAGCT | 55666 |
rs567118994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629663 | AAAGAGAAAAGGTAT[C/T]GATGGCAGTAAGAGT | 55666 |
rs567141388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592012 | TCACTCGAGCAAAGC[A/G]CACACTTCATTGGGG | 55666 |
rs567153930 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635744 | CCTGGCAAAACTGCA[A/G]AGACTGTCACAATGC | 55666 |
rs567190234 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558957 | AATTCCAGGTGCCAC[A/G]TAGAGGCGAGAGGTC | 55666 |
rs567209234 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558413 | TCTGCAGTTGCTGCA[A/G]CTGTGTGGCTTGGTA | 55666 |
rs567220028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579734 | AGCAGTACATGCCCA[C/T]GTCAGTATTTCCCTT | 55666 |
rs567224730 | snp | C/T | 0.316668 | 0.240947 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602932 | ATATATACACACACA[C/T]ATATATATATACACA | 55666 |
rs567232293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578931 | AATGTTCCATATTTA[C/T]TTATTTAGAGACAGG | 55666 |
rs567232559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585042 | AGGCGTGGCAGCGTG[C/T]GCCTGTAGTCCTGGC | 55666 |
rs567250251 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634124 | CAATCCACCTGCCTC[A/C/G]GCCTTCCAAAGTGCT | 55666 |
rs567271724 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607006 | GCACATTCCGAATCC[C/T]AGCTTCTGTCCCACA | 55666 |
rs567276228 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633603 | TGACAACATGAACAC[A/G]CAGCCTCTTGGTAAC | 55666 |
rs567282607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567896 | GTCTGGCCAACATGG[C/T]GAAACCCCGTCTCTA | 55666 |
rs567294213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600075 | CTGGAAGGCTGAAAT[A/G]TAACAGCCAGATCTG | 55666 |
rs567299192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595305 | CAGGCGTGGTGGTGT[G/T]CACTTACAATTCCAG | 55666 |
rs567322005 | in-del | -/A | 0.305934 | 0.243663 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589532 | GACAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 55666 |
rs567325856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585113 | AGGCGGAGGTTGCAG[C/T]GATCTGAGATCGCAC | 55666 |
rs567327828 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584895 | AACGAGGCCCAGCAC[A/G]GTGGCTCACGCCTAT | 55666 |
rs567478787 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628471 | TGAGCCGAGATCATG[C/T]CACTGCACTCCAGCC | 55666 |
rs567498832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623268 | CGAGGCCAGGAGTTC[A/G]ACACCAGCCTGGTCA | 55666 |
rs567506791 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613390 | ATCTCATCCTCCACC[A/G]CGTTGGGAGCGCCAA | 55666 |
rs567522960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618431 | CCCCGCAGCCGCCCC[A/G]TCTGGGAAGTGAGGA | 55666 |
rs567566032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594261 | GCCTGGGCGAAAGAG[C/T]GAGACTCCGTCTCAA | 55666 |
rs567600379 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557684 | GGAGAGCAGACAGCC[C/T]GCGGTGGGCAAGCTG | 55666 |
rs567612967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566981 | TGGAAGCTGGCCAAG[A/C]CTTCTGGGCCAAGGC | 55666 |
rs567616780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588752 | CACTTCTGGTGAGAA[A/G]CCCTACGCCATGGAA | 55666 |
rs567686001 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592812 | AACATGGTGAAACCC[C/T]GTCTCTACAAAAAAT | 55666 |
rs567688228 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580266 | CACATCGCCGACAGA[G/T]CCCCAGCCTTCCAGC | 55666 |
rs567694671 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610491 | GATCGTGGCTCCCTG[C/T]AGCCTTCACCTCCTG | 55666 |
rs567736674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612439 | AGGCCCCTGGGAGGA[C/G]ACACAAATGGAAGAG | 55666 |
rs567740242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583735 | TTCCTCGTTCTCTTA[A/C]TGGCTGCATATGGGA | 55666 |
rs567800796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583169 | CTTGGAAATATCTAT[C/T]AAAACTCGAAAAACC | 55666 |
rs567814008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572274 | ACTCACTGCAAGCTC[C/T]GCCTCCCAGGTTCAC | 55666 |
rs567827230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577807 | CTCTCTGCACACCTG[C/T]CAGGCCTCCAAACCT | 55666 |
rs567834978 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595932 | TTGGGGTTTGTGTTT[A/G]TATAGTTTTATGCTG | 55666 |
rs567837550 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605845 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 55666 |
rs567854159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611306 | GCCTGGGAGACGAGA[C/G]TGAAATTCCACTCAA | 55666 |
rs567915622 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605150 | GCCAGGCGTGGTGGC[A/G]GGCGCCTGTAGTCTC | 55666 |
rs567916197 | in-del | -/AGA | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626058 | GGAGGCTGAAACAGG[-/AGA]ATCGCTTGAACCTGG | 55666 |
rs567976554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626567 | AACAGGACCAGGCAC[C/T]GCGGCTCCCGCCTGG | 55666 |
rs567996524 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571291 | GTCCGCTTTGGACAG[A/G]GCTCCGGTGGGGCTG | 55666 |
rs567998146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606415 | CAGTTTCCTCACAAC[C/G]ACTGAGGATTTTAAA | 55666 |
rs568040339 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637279 | CCTCGGAAACCCAAG[C/T]GGCACAGGAAAGTCC | 55666 |
rs568144320 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564441 | CTCCAGCCTCGGCAA[C/T]AGAGTGAGACCCTGT | 55666 |
rs568185491 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577857 | CCTTGTCCCCAAGGC[C/T]ACAGGGAACTGACAT | 55666 |
rs568231350 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627934 | GAAAAAGACTCCATC[G/T]CAAAAAAAGAAATTT | 55666 |
rs568232337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632805 | GTCCGCTTTTAGTAA[A/G]GTAACTAAGCCTAAT | 55666 |
rs568268100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586749 | CCAATGAGACAAAGA[C/T]TTAAGGAAGACTGTC | 55666 |
rs568268396 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611166 | CTCTACTAAAAATAC[A/G]AAAATTAGCCGGACG | 55666 |
rs568303155 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557209 | CTTCCCACAAGAGGA[A/G]GTGGCTGAGCCTCCC | 55666 |
rs568331475 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599608 | ATAATCTAGAGATTA[G/T]TTTTCATGGTCTGAG | 55666 |
rs568352404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597399 | CTCACGCCTATAATC[A/C]CAGCACTTTGAGAGG | 55666 |
rs568379613 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560246 | AACATGGCGAAACCC[C/G]GTCTCTACTAAAAAT | 55666 |
rs568391792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593815 | CAGTGCCCACTGCCT[A/G]ATGCCCCAGCTGCTC | 55666 |
rs568404599 | snp | C/G | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635928 | CGAGGGACTGGTTTT[C/G]TGATTTGTCACTGAT | 55666 |
rs568434806 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572766 | GGACCTGTGCCCTGT[C/T]TATCCTCCAAAAGCA | 55666 |
rs568452062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603752 | CATTTTATTTTTCTA[C/T]TGGATTTCAAGTGTA | 55666 |
rs568452803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587258 | GCGGGAGGACTGCTC[A/G]AGGCCAGGAGTTCAA | 55666 |
rs568456747 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581915 | CAGAGCTAGTAGCCT[C/T]GCTATGCCCTGGATG | 55666 |
rs568502633 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559469 | GGCCCACCAGAGACT[A/G]CCAGAGTGTGGGCAT | 55666 |
rs568535850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630481 | TAGTGACGGAGTGTC[A/G]TATTTCCCAGGCTGA | 55666 |
rs568545479 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636487 | GCACTTGCTGGGAAG[C/T]GGGAGAGCAGGAGGA | 55666 |
rs568549006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620483 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA | 55666 |
rs568549960 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575687 | CTCCCAAGTCAGTGC[C/T]GGTGCTGCAGGGCCA | 55666 |
rs568566379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597652 | AGTTGGGGTGGTGGC[A/G]CATGCCTGTAATCCC | 55666 |
rs568573247 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629881 | CGGCTTCCATCTGTG[A/G]TCTTTTAGCATCTGG | 55666 |
rs568593958 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619368 | GGCAACACAGTGAGA[C/T]TCCGTCTCAAAAAAC | 55666 |
rs568651540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592646 | GAAACTGTAATTCTA[A/G]AAATGTGCCAGTTCT | 55666 |
rs568667439 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600006 | GCACAGAGGAGCCAG[C/T]AGGGGTGCGGCTGGG | 55666 |
rs568689746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620831 | TAGATAATGGTTACG[C/T]GTTCCAGATTTAAAC | 55666 |
rs568701419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625249 | GTGCAGGGACCATGA[A/C]AGGAAAGGCTAAAAA | 55666 |
rs568708226 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569361 | CTGTGCACCGGCCTC[A/G]ACGTCGGACAAAAAG | 55666 |
rs568744351 | in-del | -/AGCACAAGACCT | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589576 | CGGATGGGTGGCCAC[-/AGCACAAGACCT]AGCACAAGACCTAGC | 55666 |
rs568800738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569530 | CAGGAGCTGACTTTG[C/G]TCAAGAGAGATTCGT | 55666 |
rs568812218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619067 | GGACACAAACACTGC[A/G]GAAGGCCGCAGGGTC | 55666 |
rs568816803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569258 | TCCATCAAAGGGAAC[C/T]GTTATCTATTAGTGT | 55666 |
rs568821674 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585104 | GAACCCGGGAGGCGG[A/G]GGTTGCAGTGATCTG | 55666 |
rs568848868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596873 | TAATCCCAGCACTCT[A/G]GGAGGCCAAGGCAGG | 55666 |
rs568882541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590767 | CATGGCTGTCAAACA[C/T]GCATCAGAAAGCAAA | 55666 |
rs568908156 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615580 | TGCACTCAGACAGCA[C/G]CCAGCAACACAGAAC | 55666 |
rs568914802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602086 | TGCATGCATGCGTGT[G/T]TGTATGTGCTTACAC | 55666 |
rs568953862 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620898 | AAGTGAAAAATGTGC[C/T]TGTAGTCCCAGCTAC | 55666 |
rs568996794 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581179 | ACATGGCGAAACCCT[C/G]TCGCTACTAAAAATA | 55666 |
rs569024117 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560399 | GCCTGGGCGACACAG[C/G]GAGACTCCATCTCAA | 55666 |
rs569031811 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614775 | CAGTCCACAGAAGCC[G/T]CCTGGGGTCCCAAGT | 55666 |
rs569052186 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618902 | GTTGATCTATGACCT[G/T]ACCCCAACCCTGTGC | 55666 |
rs569068555 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619474 | GAATCGCTTGAACCC[A/G]GGGGGGCAGAGGTTG | 55666 |
rs569133945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575160 | GCTGGAGTGCAGTGG[C/T]GCGGTCTCGGCTCAC | 55666 |
rs569171712 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621550 | TGCCCAGATGGTTTC[A/G/T]ATGGGAGCCAGCACC | 55666 |
rs569175555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628623 | TACAACAAAGGCTAA[C/T]GGATGTTTTTCAGTC | 55666 |
rs569192923 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617902 | CTAACCAAGTGATCC[A/G]CCAGCCTCGGCCTCC | 55666 |
rs569200192 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635269 | TCTTGAACCCGAGAG[A/G]CGGAGGTTGCAGTAA | 55666 |
rs569317478 | snp | A/C/G | 0.00279258 | 0.0372817 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594632 | TACAAAAAATTAGCC[A/C/G]GGTATGCTGGCAGGC | 55666 |
rs569341466 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574467 | GGCCTACACACCATT[G/T]TAAAAGGCAATTACT | 55666 |
rs569342132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601450 | ATTTTTAGTAGAAAC[A/G]GGGTTTTGCCATGTC | 55666 |
rs569373249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573519 | TGGTGAGTTACCTCA[A/G]ATGATTGTTAACAGT | 55666 |
rs569381194 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595857 | CCAAAAAAGTGGACT[G/T]TTAATGAGAGCACTG | 55666 |
rs569386059 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558238 | ATGGCCCTCACAAGA[A/G]GCACAGCCCCTAACG | 55666 |
rs569411745 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558833 | CAGACAAGGGGGTAA[C/G]CAAGAGCTCCCAGCC | 55666 |
rs569454152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634814 | AGTCTTGAACTCCTG[A/G]CCTCGTGATCCGCCC | 55666 |
rs569471707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588222 | GTATCAGTAAACTGC[A/G]GGACAACTTCAGGCA | 55666 |
rs569500594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635125 | GGCGGGCGGATCACG[A/T]GGTCAGAAGTTCGAG | 55666 |
rs569531129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594908 | GACTGCACCACTGTG[C/T]TCCAGCCTGGGTGAC | 55666 |
rs569585433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563050 | CCTAGGAGTTTGAGA[C/T]CAGCCTGGGCAACAT | 55666 |
rs569594361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584451 | TTCCAATCTGAAAAG[C/G]GTATTTAAAAATAAT | 55666 |
rs569623141 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599507 | TCTTTCCTAAAGACA[C/G]TAAAACTGTGTGGAC | 55666 |
rs569640035 | snp | C/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560820 | GCACGGTTTTGCCTC[C/T]CACTCGCAAGGTACG | 55666 |
rs569658427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589813 | GACCAGTCTGGGCAA[C/T]ATAGTGAGACCCTAT | 55666 |
rs569679590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600015 | AGCCAGCAGGGGTGC[A/G]GCTGGGGTCTGTTTC | 55666 |
rs569691276 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557075 | AGGAGACTGGCAGCC[A/G]CTGTGTTCACCTGGG | 55666 |
rs569696296 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557736 | CGCTTCAACCCAGCT[C/T]CTCTCCACCCTTCCT | 55666 |
rs569702447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566359 | TTCATATATGAGAAA[A/C]GGATAAAGCCTTCAG | 55666 |
rs569761018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631967 | ACCATACCCAGCTAA[C/T]TTTCTTTTTTTTGAG | 55666 |
rs569788863 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558061 | AGGCAAAGAAGCATC[A/G]AGATGCCCACCACTC | 55666 |
rs569862174 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626253 | CCCCGGAGGCGGAGG[C/T]TGCAGTCAGCCAAGA | 55666 |
rs569905120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617611 | TCGGGAGATCGAGAC[C/T]ATCCTGGCTAACACG | 55666 |
rs569912908 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627547 | GAGTTCGAGACCAGC[A/C]TGACCAACATGGTGA | 55666 |
rs569967689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598883 | CTTTAAAGATGCCCC[A/G]ATGAATGAAAAACCC | 55666 |
rs569969982 | snp | C/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557882 | GTGTCAGCCATGGCC[C/G]TGACCACTTCAGAAG | 55666 |
rs569999609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560191 | GGGAGGCCGAGGCGG[A/G]TGGATCACTTGAAGT | 55666 |
rs570018846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593768 | TCTAAATGACATGAG[C/T]GCCTTTGTTCTCTGC | 55666 |
rs570075972 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614981 | TGCAGGCCCTCAAGG[-/AC]ACACAGACACTGGGG | 55666 |
rs570082158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593234 | ACTACAATAGTGTAA[A/G]CTGAGGCAAGGGCAC | 55666 |
rs570104173 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599476 | GATGCTGACTCCTTG[C/T]TAGAAACAGGATGTT | 55666 |
rs570114126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582806 | TGTGATGGGCAGGAG[A/G]TCCCAGCCTGCCCAA | 55666 |
rs570117068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583047 | GCCACTGCCACGTGA[C/T]GCAGAGTGTGTGTGA | 55666 |
rs570118588 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81566597 | ATGTCAAATACCCGA[C/G]TGAGTGGTTTTGAGA | 55666 |
rs570140316 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637382 | AATTGGGGAAACAGC[A/G]TTCCAAACTTCTCTC | 55666 |
rs570163971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596770 | TGGGTTTAGCTCTAT[A/G]AGACCAAGAGATCCG | 55666 |
rs570169688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616119 | GTCAAGAGATTGAGA[A/C]CATCCTGGCCAGCAC | 55666 |
rs570189831 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622088 | GATGAGGAAAGAGGA[A/T]AAAACTCGGCAACCT | 55666 |
rs570201631 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623416 | GCTGCAGTGAGTCGA[C/G]ATCATGCCACTGCAC | 55666 |
rs570211272 | in-del | -/TTTTGT | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622562 | TAATGGCTATCCTTG[-/TTTTGT]TTTCAGACAGTCTCG | 55666 |
rs570299897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616505 | GGAGGCCGAGGCAGG[A/G]GGATCATGAGGTCAG | 55666 |
rs570323183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611769 | TAGAGACCATCCTGG[A/C]AAACACGGTGAAACC | 55666 |
rs570333526 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610398 | ATGGCACATGGATAA[A/T]CATTTATATTTTAAT | 55666 |
rs570347816 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603193 | AAAGAAAAAGGTTTT[A/C]AATTCTAGGGGCTAC | 55666 |
rs570393461 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581739 | AGATTCCAGACACTA[C/G]AGCCACTGTCCCATG | 55666 |
rs570394176 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637776 | CCGTCTCTACTAAAA[A/C]TACAAAAATTAACTG | 55666 |
rs570397881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631333 | GAAGATCTCTTTAGC[A/C]TAGGAATTCGAGATC | 55666 |
rs570405094 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559009 | TGTCAACAGGATTAG[A/G]CGTGAGGAGCCGCTC | 55666 |
rs570435129 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583024 | GCCCATGTGCGCCAG[-/C]CACAGCAGCCACTGC | 55666 |
rs570464445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620420 | AGAAATGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 55666 |
rs570465953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572621 | CAGCCTGAAAAAGCA[G/T]TCGTGCTCTCGGGCA | 55666 |
rs570527085 | snp | A/C | 0.000166058 | 0.00911051 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596258 | CTAAGACAAGAGAAG[A/C]AGCCTATCAAATTTT | 55666 |
rs570549219 | snp | A/C | 0 | 0 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569210 | AGCCCAAATTAACGA[A/C]TCCTAGCAATTCTGA | 55666 |
rs570559110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575840 | CTCTTAAGACTGGGA[A/C]TATGCTATAATAAGT | 55666 |
rs570561026 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570283 | ACTCTTCCTCAGGAT[A/G]AAGATGATCGGAGTA | 55666 |
rs570576740 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604084 | TTCTTTCCCCTCCAA[A/T]CAAATCTTAAATTGT | 55666 |
rs570594383 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575956 | ATGAGTGAAAAGGCT[C/T]GTTTTAAAAAGTTGC | 55666 |
rs570602470 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634679 | CAACCTCCACCTCCC[A/G]GGTTTGAGCGATTCC | 55666 |
rs570634978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569444 | TCTCCCTCTGCTATG[A/G]AGGAACGAAAGGCTG | 55666 |
rs570687745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559835 | CCTCCCGGGTTCAAG[C/T]GGTTTTCCTGCCTCA | 55666 |
rs570730269 | snp | A/G | 3.31389e-05 | 0.00407042 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597321 | ATCCAGCCAACCTTA[A/G]AAAAAGGAAAGTAGC | 55666 |
rs570736907 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596343 | CCAGGAGCAGTGACT[C/G]ACACCTCTAATTCCA | 55666 |
rs570752541 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591870 | CTGGTTTTTTAACCA[A/G]ATCCCCAGCAAGTAA | 55666 |
rs570753643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598575 | CTCCACCTCAAGGCC[A/G]GAAGGAAGCATCTGA | 55666 |
rs570778256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608520 | GTTCTAGACCAGCCT[A/G]GGCAACATAGTGAGA | 55666 |
rs570841439 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629938 | ACTCTTCACCTTTCA[A/G]TACCCAGCTCAATCC | 55666 |
rs570852251 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592532 | ACCTTTCAGTAAATA[A/C]CAATTCCAGAGGTGA | 55666 |
rs570872793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628080 | AGCCAGGCATGGTGG[C/T]GGGCGCCTGTAGTCC | 55666 |
rs570878337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612923 | GGATGCGCACACACA[A/G]CCACCTGCCCCTTCC | 55666 |
rs570880218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563702 | GCAAGGAATGCTTGA[G/T]GCCAAAGTTTGAGAC | 55666 |
rs570889970 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558801 | CCTCACAGGCAGGGT[A/G]CCTGCCACCAAGCAG | 55666 |
rs570951451 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558480 | AACTGACTGGTGCCC[C/T]CGTCCACACTCATCA | 55666 |
rs570959529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634764 | CTAATTTTTTATTTT[C/T]AGTAGAGACAGGGTT | 55666 |
rs570986231 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581223 | CAGGCATGGTGGCAG[A/G]TGCCTGTAATCCCAG | 55666 |
rs571034018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581286 | CCTGGGAGGCGGAGG[C/T]TGTAGTGAGCCGAGA | 55666 |
rs571094165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625197 | TCAGAGTAAAGCTGA[C/G]AATTCTAGATTGAGA | 55666 |
rs571098509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586123 | GAGGGAGGAAGGGGA[A/G]GCAGGGGCCTGAATC | 55666 |
rs571149541 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582387 | CCTAAGCATCTAGCG[C/G]TGTTCTGTGTGTGTA | 55666 |
rs571181411 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590118 | CCTCTGTCTTCCAGA[A/C]ACCTACACGGCCGCC | 55666 |
rs571204920 | in-del | -/CAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621219 | TCTGGAAATGAACAT[-/CAA]CAACAAGAGGTTTCG | 55666 |
rs571218105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574107 | CAAACTAAATCACCA[C/T]TTCCAAAAATACAGG | 55666 |
rs571224679 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623824 | CAAAACTCAATTCCA[A/G]TTCTGAAACCTAACA | 55666 |
rs571240418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601307 | GTTTGCTGGGTATTA[C/T]CCATATGGAGGTCAT | 55666 |
rs571267022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562957 | AAAAAAGGAGGGGGG[A/G]AAAAAAAAAGGTCAG | 55666 |
rs571280748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595447 | AAAAAAAAAAAACCC[A/G]TTTTGCTTTTTTTTT | 55666 |
rs571304493 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617486 | CAAGACTAGCCTGAC[C/G]AACACAGAGAAACCC | 55666 |
rs571307206 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622750 | GAGATGGAGTTTCAC[C/T]ATGTTGGCCACGGTG | 55666 |
rs571327903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579830 | GCTCTCCCTGGCAGT[A/G]AAACCCCCCGAAAGA | 55666 |
rs571365453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617817 | GCGCGCGCCGCCACG[C/G]CTGACTGGTTTTCGT | 55666 |
rs571390949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585610 | AGGTTGCAGTGAGCC[A/G]AGATCAGGCCACTGC | 55666 |
rs571411140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590672 | TTATAGTTTTGGATG[A/G]AAAAAAACCCTCAAT | 55666 |
rs571436077 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557605 | GGCCACCTAGGCTCA[A/C]AGCTCATCTCAGGAC | 55666 |
rs571451881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624287 | GCTAGGCGTGGTGGC[A/G]GACACTTGTTATCCC | 55666 |
rs571463058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613813 | AGGGCCTCTCCTCCC[A/G]CCTCTCACCCTCTGC | 55666 |
rs571465706 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561168 | TTCACCATGTTGGCC[C/T]GGCTGTCTCGAACTC | 55666 |
rs571497885 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618475 | GCAGCCACCCCGTCC[A/G]GGAGGAAGGTGGGGG | 55666 |
rs571521608 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583777 | TGTAGACTCTCCTCC[C/T]TCCTGAAGGACAGTC | 55666 |
rs571526585 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613263 | TAAATATTTCCCTTT[A/C]TTCACCCATTAAGAT | 55666 |
rs571526778 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614170 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 55666 |
rs571585570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622620 | CAGTGGCATGATCTC[A/G]GCTTACTGCAACCTC | 55666 |
rs571590876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634217 | CCATGTCGGCCAGGC[A/T]GGTCTCAACTCCTGA | 55666 |
rs571612116 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592228 | GATGTGGGACGGGAA[A/T]GCAACAAGTACAATT | 55666 |
rs571617439 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559079 | ACCAGCCGTGGCGCC[C/T]GCTCTCCAGGGAGGA | 55666 |
rs571625111 | in-del | -/A | 0.32153 | 0.239548 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562956 | AAAAAAGGAGGGGGG[-/A]AAAAAAAAAAGGTCA | 55666 |
rs571654851 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597708 | GAATCACTTGAACCC[A/G]GGAGGCAGAGGTTGC | 55666 |
rs571702210 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598675 | TGTGATCCTTAGGCC[C/T]GCCTCTGCCTGTGAA | 55666 |
rs571707452 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576371 | TTTTCAACCAAACAC[-/A]AGATTGAAAATACAG | 55666 |
rs571714256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598011 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGT | 55666 |
rs571715829 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558458 | ACTGAGGTTTACTTC[A/G]AGGGAGAACTGACTG | 55666 |
rs571730234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607056 | CACACAACTACTTTC[C/T]TACCAAACTGTGGTG | 55666 |
rs571754764 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627417 | AAATTGATGCATGGT[-/G]GGGAACAAAAATGAA | 55666 |
rs571769502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578536 | GAGGTTTAATTGACT[A/C]ACAGTTCAGCATGGC | 55666 |
rs571877170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600793 | TCCTTGGATAAGTAG[C/T]TTCACTCCAAACAGG | 55666 |
rs571905988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573440 | CTAATGAGAAGCCCC[A/T]GGCCCCCATTTGGCC | 55666 |
rs571944637 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636376 | GAGCAAAGCCGGCAA[A/G]TTACTGTGTTTTCAT | 55666 |
rs571953721 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621118 | GAAAAGGAAAGAAGG[A/T]AGGAAGGAAAGAAAA | 55666 |
rs571964816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604940 | GTCCAGCCTGGGTGA[C/T]AGAGTGAGACCCCTT | 55666 |
rs571979295 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565370 | GAGTCTCTACTCGTT[G/T]CATTGCCGATGGCAC | 55666 |
rs572030887 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637355 | CTACTGCTGCGTATT[A/G]TAGCGTATTATAATT | 55666 |
rs572034138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632289 | CTAGCTGATTTTTTA[C/T]AGTGAAACATTTCAA | 55666 |
rs572105252 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588298 | CAAAAAGAGAAAACA[C/T]TGAGTAGCTGCAATT | 55666 |
rs572173720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625108 | CAAGAGCACACTTTC[C/T]AGCAGTGGTCATCAC | 55666 |
rs572189614 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581968 | GTCTCTGGGACGTGC[A/T]GACAGCAGAGACATG | 55666 |
rs572195454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626713 | TCACGTGGGAGGATC[A/G]TTTGAGCCCGGGAAG | 55666 |
rs572264933 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611884 | AGAATGGCGTGAACC[A/G]GGGGGACGCAGCTGG | 55666 |
rs572270831 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611961 | CGAGAGTCCATCTCA[-/A]AAAAAAAAAAAAAAA | 55666 |
rs572289723 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588377 | CTCCACCCCTATCCT[C/T]GAGACAGGGTCTCGC | 55666 |
rs572309303 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626690 | AATTAAGAAATTAGC[C/T]AGGAAGCTCACGTGG | 55666 |
rs572312557 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557309 | TAAAATAAAGTGCAT[C/T]ACTGAACAAAGAGTA | 55666 |
rs572356612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576964 | GTACATAGTAAGCTT[C/T]GGCAACATAATCCTA | 55666 |
rs572370354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585823 | GAAATCCTGATTCTA[C/T]TAAAAATACAAAAGA | 55666 |
rs572420997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615257 | GACATGTGCCACCAC[A/G]CCCAGATACTTTTTG | 55666 |
rs572423968 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592188 | ATGCCACATGGCTCA[C/G]TCTGAACCTTCCTGT | 55666 |
rs572451386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624922 | AGAGATGAGGCTGGC[A/G]AGGCAGACAGGGCCG | 55666 |
rs572491093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586808 | AGATGGCACCCCTAA[C/G]GGGTTACACTGTAGA | 55666 |
rs572545546 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614208 | CTTGAACCCAGGAGG[C/T]GGAGGTTACAGTGAG | 55666 |
rs572546809 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632897 | AAAAGGCTCCACCCA[A/G]TATGTTCTCAACTTT | 55666 |
rs572583316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609728 | AAGAAATGCCACAAG[A/G]TGAGGCAAGAGATGC | 55666 |
rs572595789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610118 | AACCACTCACTACAG[C/T]CAAGTGCGTGGACTC | 55666 |
rs572601267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563327 | ATCCACCTGCCTCAG[A/C]CTCCCAAAGTGCTGG | 55666 |
rs572656195 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604325 | AATAGTGGCAAATGT[A/C]CCGGTTGTGTAAGAA | 55666 |
rs572661019 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635336 | AGAGTGAGACTCCAT[C/G]TCAAAAAAATAAAAT | 55666 |
rs572696413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564943 | GCACTCGGGCTGCAC[A/G]AGGCACCACGGTGCG | 55666 |
rs572708872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570473 | GGCACCCCCAGAACA[C/T]GTGCTAGTGAGTGAG | 55666 |
rs572720544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574308 | GTGTCATGCTATTCT[A/C]TTTCAAACTTAACTA | 55666 |
rs572743231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608295 | ACCACAGAATCAACA[A/G]GCCACCATCACAGAT | 55666 |
rs572772731 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636732 | GGGAGGGACACGGAC[G/T]GGAAGCAGCCGAGGG | 55666 |
rs572779873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613917 | GTTGCATGTATCTCC[A/G]CTGCTTTCTCGGCGT | 55666 |
rs572788982 | snp | A/C | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563273 | AGAAATGGGGTTTCA[A/C]CATGTTGGCCAGGAT | 55666 |
rs572790456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614458 | ACAATGACAAGTATG[C/T]ACACCATCTGCCAGC | 55666 |
rs572790809 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604346 | TGTGTAAGAAAATAT[C/G]CTTATCCTTAGTAAC | 55666 |
rs572818092 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558990 | TCCAACACGGCGGGG[A/G]ACTTGTCAACAGGAT | 55666 |
rs572839977 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585882 | TAGTCCCAGCTACGC[A/G]GGAGGCTGAGGCAGG | 55666 |
rs572851159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608629 | GTGACCCCTTCTCAT[C/G]TTTACTTCTCTCATT | 55666 |
rs572890366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569284 | AGTGTCATCTCTAAA[C/T]GAACACTTGGAAACT | 55666 |
rs572901727 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605031 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCATGAGG | 55666 |
rs572910106 | snp | C/T | 0.000216093 | 0.0103923 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600326 | CCCCTGCTTGGCTGC[C/T]GGATGCCTCAGTACC | 55666 |
rs572915461 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593398 | GCTGTGCTGTCCTCA[A/C]GAGTCAGTCCAGAAG | 55666 |
rs572918466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607172 | GCATGAGGCTCCTAC[A/G]GGTTTCATTAAATTG | 55666 |
rs572999325 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625558 | CTGAACGGGCTTATC[A/G]GCAGAAGGGAGAGAG | 55666 |
rs573064294 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637793 | ACAAAAATTAACTGG[C/G]CGTGGTGGCGGGCAC | 55666 |
rs573064839 | in-del | -/AAAAG | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631190 | AAAATTTAAACTTAA[-/AAAAG]AAATTAAAATTAAAA | 55666 |
rs573068263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597085 | GCCACTGCACTCCAG[C/T]CTGGGCAAAAGAGCA | 55666 |
rs573088221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591797 | TGGGAAGGATCACAG[A/G]GCCTACAAAGAGGCA | 55666 |
rs573121386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596479 | TGGGTATGGTGGTGC[A/G]CACCTGAACCCAGGA | 55666 |
rs573148851 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558564 | GTCTCTCTCACTCCC[C/G]TTTTGTGCAGTTTTT | 55666 |
rs573150483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633973 | CCGGGTTCTAACTTT[C/T]CTGCCTCAGCCTCCT | 55666 |
rs573167594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618569 | CCGGCCAGCCGCCCC[A/G]TCCGGGAGGGAGGTG | 55666 |
rs573185709 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557666 | TGTGACAGCTGCTAG[C/G]AGGGAGAGCAGACAG | 55666 |
rs573187009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595034 | GCAGTCAGCTTGAAC[A/G]CTTTTCTTTCTTTTT | 55666 |
rs573204954 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589809 | TTGAGACCAGTCTGG[A/G]CAACATAGTGAGACC | 55666 |
rs573208150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597432 | GAGGCAGGAGAATCA[C/T]GAGGTTAAGAGATCG | 55666 |
rs573208674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618276 | TGCCCGGCCGCCCAT[A/C]GTCTGAGATGTGGGG | 55666 |
rs573241661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628268 | TTCATGGCTGGGCAC[A/G]GTGGCTCACACTGAA | 55666 |
rs573279919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634392 | TTCCTCACAATCTGA[A/G]ACATTCAACGAGATC | 55666 |
rs573290125 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595599 | ACCCAGGCTGGAGTG[C/T]ACTGGCACAAACTCA | 55666 |
rs573344390 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590809 | CACAATCAAAAAAGG[G/T]GAGGGAGGAGATAGA | 55666 |
rs573384366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577627 | CTGTATCTCTTGCCT[A/G]AGCTTCCAGACCTGA | 55666 |
rs573392952 | snp | C/G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558279 | GGCGGTGCAGTGGGA[C/G/T]GAAGCAGCGTATTGG | 55666 |
rs573431808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584933 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATTGC | 55666 |
rs573432149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628677 | AAATAGTCTGGGGGA[A/G]TCCATGGGAAAAGTA | 55666 |
rs573472095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578160 | CCAGCAGGAACATTC[C/T]AGAACTCACTTTCCA | 55666 |
rs573472612 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580555 | CTTATCACTCTCTGT[A/G]TGGGGAACAGGCTGC | 55666 |
rs573517523 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622317 | AAATTTAATGAAATG[C/T]TAAAGTATCACTACA | 55666 |
rs573521678 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558858 | CCAGCCAGAAAAACA[C/T]GGGGGCAGGGAGGCC | 55666 |
rs573558799 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579989 | CACCCCTGAGCTGCT[A/G]AAGGCAAAGCCTCCT | 55666 |
rs573587536 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557824 | AGAGCAGATGAGCTG[C/T]TTGGGCCTTCCACTT | 55666 |
rs573604846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588548 | AGACACAGTCTCGCT[A/G]TGTTGCCCAGGCTGG | 55666 |
rs573629506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579305 | ACTGCTTGAACCAGG[C/G]AGGCGGAGATTGCAG | 55666 |
rs573629520 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585203 | AAAAAAAAGAGTATG[C/G]TATTAGTTCTGGTTT | 55666 |
rs573663529 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558886 | GCCAAACAAAAAGCA[C/T]TGAAAATAAAGAGAA | 55666 |
rs573719633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627316 | GAAATGGCATGAACC[C/T]GGGAGGCAGAGCTTG | 55666 |
rs573745618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622819 | GCCTCCCAAAGTACT[A/G]GGATTACAGGCGTGA | 55666 |
rs573746451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612894 | AAATGAGAGACACAG[C/T]ACTCACCTCACATGG | 55666 |
rs573784075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622375 | AAGAGTATTCACCAA[A/G]TTTGGAAAGTGCCCA | 55666 |
rs573862122 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573153 | GGATCACATTTTCTA[C/T]CTAAATCATCACTTA | 55666 |
rs573928901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566096 | CCCAACACTTTCAGA[A/G]GCAGAGGCAGACAGA | 55666 |
rs573944353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616558 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 55666 |
rs573950181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576214 | GTATCATGCATAAAT[A/G]GATTATGGATCTCAA | 55666 |
rs573970002 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610843 | TGTAGTCCCAGCTAC[C/T]CGGGAGGCTGAGGCA | 55666 |
rs574001424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560456 | GCTCATGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 55666 |
rs574045619 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571840 | GCATTTCAGCAACAC[C/T]GCATGCTCAGTGATT | 55666 |
rs574059694 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576820 | AAGCACAGAGAGCGG[G/T]GTCCTGGGCCTGCCT | 55666 |
rs574087220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571290 | CGTCCGCTTTGGACA[C/G]AGCTCCGGTGGGGCT | 55666 |
rs574116830 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632113 | CCTGAGCAGCTGGGA[C/T]TACAGGCGTGCACCA | 55666 |
rs574136177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604992 | TGGGCTGGGCGCAGT[A/G]GCTCACGCCTGTAAT | 55666 |
rs574150301 | snp | G/T | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635465 | CACCAAGAGGGCCCC[G/T]GACTGGAGAGATGAT | 55666 |
rs574227721 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633227 | AAAACGTTTTCACAA[C/T]ATATAGCATTAGGTA | 55666 |
rs574265069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638813 | CAAAATATCTCAAGC[A/G]CTGATCTGTTTTTTA | 55666 |
rs574269976 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557443 | GCTGGTGGAGGACAA[C/T]GGAAACTATAATAGC | 55666 |
rs574276329 | in-del | -/CTGG | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608654 | TCATTCACACGTTCA[-/CTGG]CTGGCTATAAGCAAC | 55666 |
rs574302354 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636249 | GTGCTGACATCACAG[A/G]CGTGAGCCACTGCGC | 55666 |
rs574310900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594091 | ATCCTGGCTAACACG[A/G]TGAAACCCCGTCTCT | 55666 |
rs574320492 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570375 | GTCCCAGCTGAAGAC[A/C]GGGGAGGTGCTGACC | 55666 |
rs574327541 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619696 | TCAGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT | 55666 |
rs574348502 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597513 | AATTAGGCCGGGTGC[A/G]GTGGCTCACGCCTGT | 55666 |
rs574366329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626903 | GAGACCAGACTGGCC[A/G]ACATAGTGAAACCTC | 55666 |
rs574397582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620696 | GAGGAGGGAGAAAAA[A/C]AGGCCAAGCAACAGA | 55666 |
rs574420258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599709 | TCTACATTAATTTAT[C/T]AAAATTGTTCCTGGG | 55666 |
rs574453685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591714 | TTTGTGTAACCCTGC[C/T]GGAATGGCTGGCAGG | 55666 |
rs574487709 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636710 | AACCGGGGTCGTAAG[C/T]CCCCTGGGGAGGGAC | 55666 |
rs574508773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593333 | CCAGCTGAGAGGCCT[A/G]GACCCAGCCCTGTGC | 55666 |
rs574515279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591030 | TCACTTGCCCATGTG[C/T]TTGGTGGCATAAATG | 55666 |
rs574534678 | snp | A/C | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560709 | AACAAACAACAACAA[A/C]AAAAAACCTACCTAG | 55666 |
rs574545385 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566116 | AGGCAGACAGATCAC[A/G]AGGTCAGGAGTTTGA | 55666 |
rs574554480 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627139 | CTCACTCTTGTAATC[C/T]CGGCACATTGGGAGG | 55666 |
rs574572976 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605698 | TTCAGAGTCCAGTGG[C/T]GGGACACGGGGTTAT | 55666 |
rs574590025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564883 | GCATTTGTCCAGGGC[C/T]GTAGCTCCCGGGCAC | 55666 |
rs574621690 | in-del | -/TT | 0.245916 | 0.249967 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595453 | AAAAACCCGTTTTGC[-/TT]TTTTTTTTTTTGAGA | 55666 |
rs574639913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585750 | CCAGCACTGTGGGAG[C/G]CTGAGGCAGGCAGAT | 55666 |
rs574644747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587022 | CACACCACACACACT[C/T]AGCACGCCAGTAACA | 55666 |
rs574707446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586220 | CCTCCTGCAGGAAGT[A/G]AGTGCTGGGAGATGA | 55666 |
rs574766118 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592781 | TTGAGGCCAGAAGCT[C/T]GAGACCAGCCTGGCC | 55666 |
rs574770114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582420 | TATGTCTGCATGTTT[C/T]TGGAGGAGTCTTGTT | 55666 |
rs574800395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597070 | GTGAGCAGAGATTGC[A/G]CCACTGCACTCCAGC | 55666 |
rs574809768 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558980 | GAGAGGTCTTTCCAA[A/C]ACGGCGGGGGACTTG | 55666 |
rs574821548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580812 | GAGAGAATGGATGCC[A/G]TGAGAGCATCGCACA | 55666 |
rs574847900 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595529 | ACATATACATATATA[C/T]ATATATTTTTTTTTT | 55666 |
rs574855472 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583916 | TATACTCTAGGTATA[C/G]ATGCATTTTTAATTT | 55666 |
rs574858652 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585283 | CCTGGAGATGACCGA[C/T]GACAGAGAAGCATCA | 55666 |
rs574890157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575057 | ACCAGGATCTGAGCC[A/G]CCACAGGATAACTCA | 55666 |
rs574973528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568257 | CTAGGGCAGCAAGAG[A/G]GAGGAATGTGCAGGG | 55666 |
rs575013327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597071 | TGAGCAGAGATTGCG[C/T]CACTGCACTCCAGCC | 55666 |
rs575021628 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629117 | CTCCTGACCTTGTGA[-/TT]TCCGCCCGCCTCGGC | 55666 |
rs575072442 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605293 | CTCAAAAAAAAAAAA[A/T]AAATAATAATAATAA | 55666 |
rs575156624 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618228 | AGCGCCTCTTTCCGG[C/G]CGCCATCCCATCTAG | 55666 |
rs575162405 | snp | C/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562759 | GCCTGGGCAACATAG[C/T]GAGACCTCATCTCTA | 55666 |
rs575166327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569806 | ACAACAGAGGGCACT[C/T]TGCACCTAAGATATA | 55666 |
rs575167333 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618507 | TCAGCGACCCCGCCC[A/G]GCCAGCCGCCCCGTC | 55666 |
rs575284522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573766 | CCACTGATGTTTCCA[A/G]GAGGGCAGGAGAATG | 55666 |
rs575292207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582940 | AGAAACACACAAAAA[C/T]CCAAGGAGCCTCCCG | 55666 |
rs575301871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613547 | ACCACCTGAGCTTCA[C/T]GGAAGCCCAACTTGG | 55666 |
rs575314751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575365 | CTTGGCCTCCCAAAG[A/T]GCTGGGACTACAGGC | 55666 |
rs575315695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633932 | AGTGCAGTGGTGCGA[G/T]CTCGGCTCACTGCAA | 55666 |
rs575327460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584876 | AGACATTAAAGAACA[C/T]GGGAACGAGGCCCAG | 55666 |
rs575361391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613840 | CTGCTTGGCCCCCAC[C/T]TCCCTCAGCCATTCC | 55666 |
rs575363339 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607494 | GAAATGATATTCTGA[A/T]ACATGTCCACACTGT | 55666 |
rs575389249 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558661 | GCAGACTTTAAAATC[C/T]CACCTGGACATCGGG | 55666 |
rs575400606 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610058 | TGTGTGCAGCTTGCA[A/C]TAGGGGAATATGAGG | 55666 |
rs575444420 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558912 | GAGAAGGCTGGGTGG[C/T]GGCAGCATCGGCCCC | 55666 |
rs575461661 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623787 | AGGACGACAGAGCGA[A/G]ACTCCGTCTCAAAAA | 55666 |
rs575476407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627813 | TTGTGGTGCACACCT[A/G]TAATCCCAGCTACTT | 55666 |
rs575476452 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634269 | GCCTCTCAAAGTGCT[A/G]GGATTACAGGTGTGA | 55666 |
rs575524347 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608145 | TGAGGATTAGTGGCT[A/G]CAGCCCCTGCTGTGG | 55666 |
rs575537804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628173 | CCAAGATCATGCCAC[C/T]GCATTCCAGCCTTGG | 55666 |
rs575593656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599784 | GAAATCCTTTTCTCA[A/T]CTTCTAACTGTTCCA | 55666 |
rs575639465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562125 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 55666 |
rs575647139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602546 | TGTCTCTACTAAAAT[G/T]ACAAAAATTAGCCAG | 55666 |
rs575673494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573102 | AGAAATAAATTCATA[A/C]GAACCAAAGCTTTTC | 55666 |
rs575675842 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81566595 | TGATGTCAAATACCC[A/G]AGTGAGTGGTTTTGA | 55666 |
rs575697072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561398 | ATACTGCGTCCCCCA[C/T]TGGTGCCTTTTCATG | 55666 |
rs575757376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588465 | TCCCCAGACTCAGGT[C/G]ATCCTCCTACCTCAG | 55666 |
rs575783834 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558252 | AGGCACAGCCCCTAA[C/T]GCCCTCAGCCAGGCG | 55666 |
rs575809676 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567288 | AAATGAGGGGGACAA[C/G]CTGTGACCCCGAGCT | 55666 |
rs575812204 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623570 | TTGGGAGGCCGAGGC[A/G]GGCGGATCATGAGGT | 55666 |
rs575820162 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633423 | TGCAGAATTCTAAGG[G/T]GAAGAAGTCATCCTA | 55666 |
rs575857850 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583520 | AGAGAAAAGCCCCAC[G/T]TCCTGCCACCTGGCT | 55666 |
rs575894558 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622997 | GTTAGGAGTTCGAGA[C/G]CAGCCTGACCAACAT | 55666 |
rs575941978 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605844 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 55666 |
rs575950046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599059 | TTTGGGAGACCAAGG[C/T]GGGTGGATCACCTGA | 55666 |
rs575974599 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560431 | AACAAACAACAGGCC[A/G]GGCGCGGTGGCTCAT | 55666 |
rs576035841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584074 | ATTTTTATTGCCAGA[C/G]ACAACAACATGATAA | 55666 |
rs576106166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583349 | GTCAATAAATGCACT[C/T]ATTTATTCTCCATAA | 55666 |
rs576106216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570588 | GATGTCCCAAGGAAG[G/T]GCATCAGCTCCCATC | 55666 |
rs576146737 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616964 | GCACCAAAGTCAGTG[G/T]CTCTTCCCAAATCTC | 55666 |
rs576172663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627259 | TAGCCGGGCATGGTG[A/G]CGGGTGCCTGTAGTC | 55666 |
rs576209255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626849 | AATCCCAGCACTTTG[A/G]GAGGCTGAGGCGGGC | 55666 |
rs576259252 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624847 | GCACAAAGACCAGGA[A/G]GCAGGAAGGGTGTTG | 55666 |
rs576316925 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565965 | CCCTCACATTTCATC[C/T]CTCTGCCTCTTTCTC | 55666 |
rs576331230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | NPLOC4 | GRCh38.p7 | 17:81565440 | CGGCAGTGGGGAGCT[A/G]TGCAGAGTGGGCTGC | 55666 |
rs576385329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572487 | TGAGCCACCGCGTCC[A/G]GCCTTCACTTTTTAA | 55666 |
rs576394834 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637088 | GCTCCGCCAGCCGCC[A/G]ACGTCCCGGTGCCTC | 55666 |
rs576431706 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620142 | TACAAGAAGTAAGAC[A/G]TACAAATTTCCTTAA | 55666 |
rs576467112 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615165 | AGTGCAGTGGCGTGA[G/T]CTTGGCTCACTGGAA | 55666 |
rs576503007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582367 | CAGTGGGAAGCAGCT[A/G]AACACCTAAGCATCT | 55666 |
rs576517986 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575669 | CGTGCGCAGGCTCCC[C/G]GCCTCCCAAGTCAGT | 55666 |
rs576522504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586916 | GAGATGGACAGCTCA[C/G]CACCACCACATTTCC | 55666 |
rs576570065 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593014 | AAATAAAAGATCCTC[A/G]ATTTCACTCAGAATA | 55666 |
rs576578186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616275 | GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC | 55666 |
rs576579972 | snp | A/C/G | 7.92173e-05 | 0.00629304 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610174 | TACCCGCAGCCCCCC[A/C/G]CACTGGCCCAGAACT | 55666 |
rs576587734 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636627 | GTGGGGAAGGAGGGC[A/G]GTTTCTCTTCGCCAC | 55666 |
rs576621303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615844 | ACACAGCAAAAAAAA[A/C]CAACAAAGTCACCTC | 55666 |
rs576640721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598708 | CCTGCACCAGAAGCC[C/T]GTCACGAGGCCACAG | 55666 |
rs576643471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638106 | TGTTAGTAATTGTAT[C/T]AGTTTGCTCAGGGTG | 55666 |
rs576664246 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560005 | CTCCCAAAGTGCTGG[G/T]ATTATAGGTATGAGC | 55666 |
rs576669001 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630180 | GATGTTACTTTGGGG[A/G]AAAAAAAAAAAAAAA | 55666 |
rs576747618 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610825 | GGCGCGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 55666 |
rs576756185 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600686 | CTGCACAGCTCTGCA[C/T]CAGGAGCACTCAGGA | 55666 |
rs576778168 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585609 | GAGGTTGCAGTGAGC[C/T]GAGATCAGGCCACTG | 55666 |
rs576790194 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631730 | AGCTTCTCCTCTCAG[C/T]AAAGACTGATGGTGC | 55666 |
rs576799072 | snp | A/T | 0.000156226 | 0.00883676 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608685 | AACTGCCAGCTACAC[A/T]AAAAGGAATTTACGC | 55666 |
rs576809413 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628669 | CCAGACAGAAATAGT[C/G]TGGGGGAATCCATGG | 55666 |
rs576818577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596644 | TCTACAATTCCTAAC[A/C]ATTACCAATTCCTCA | 55666 |
rs576837907 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630997 | GCCAACATGGTGAAA[-/C]CCCCGTCTCTACTAA | 55666 |
rs576846081 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612273 | ATTCTTACATGCGTA[A/T]GAGCCCTGTGCTGCG | 55666 |
rs576860083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564675 | TGCCTGTAGTCCCAG[A/C]TACTCAGGAGGCTGA | 55666 |
rs576872841 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575228 | CCTCAGCCTCCCGAG[G/T]AGCTGGGACTACAGG | 55666 |
rs576875770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613728 | CAACTTTACCTTAAA[C/T]TCTGTGAAGCCTCCA | 55666 |
rs576912257 | in-del | -/ATT | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573418 | AGTCAAACCAAGTCC[-/ATT]ATTACCCTAATGAGA | 55666 |
rs576955532 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590952 | TGCCCCAAACTCAAA[A/T]GCTCAGGAGGCAGCC | 55666 |
rs576969234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597506 | ATACAGAAATTAGGC[C/T]GGGTGCGGTGGCTCA | 55666 |
rs577013555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569621 | CAGCAGCTCACTAAG[C/T]CCCTTCTGAATGCTG | 55666 |
rs577029768 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570335 | ACGGGGCTGGTACAC[A/G]TAGTGTTGGTACACA | 55666 |
rs577039856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591537 | AGAAAAATCTAGCAG[A/T]TGAGAATAAGAGAAA | 55666 |
rs577064727 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569842 | TAGATGCTACAGGGA[C/G]AGTGGTAAATGTGCA | 55666 |
rs577064856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593095 | ACAAGACTCTGAATG[A/C]CCGCTACACACTTGT | 55666 |
rs577066231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625037 | AGTGCCAATTAGAGA[C/G]AAGAGAGATGGGCTG | 55666 |
rs577070596 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618615 | CCCAGCCAGCCGCCC[A/G]TCTGGGAGGTGAGGG | 55666 |
rs577101712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592267 | CGCTATGGGGTCCCC[A/G]CATGGCCGTGACCAA | 55666 |
rs577204970 | snp | A/G | 0.215144 | 0.247558 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563170 | AACCTACGCTTCCTG[A/G]GTCAAGTGATTCTCC | 55666 |
rs577217580 | in-del | -/AAAC | 0.0020012 | 0.0315689 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602231 | TTTCAAAACAAAACA[-/AAAC]AAACAAACAAACAAA | 55666 |
rs577223815 | in-del | -/AA | 0.00517822 | 0.0506191 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572944 | CCACACCAATCTGTC[-/AA]AGTCTCAACTTGTTT | 55666 |
rs577224092 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594850 | ACATAGGAGGCTGTT[C/G]GGGTCGGATCACATG | 55666 |
rs577239077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592757 | TTGAGGCCGAGACAG[A/G]CGGATCACTTGAGGC | 55666 |
rs577269388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634927 | CTTGGCCGGGCATGG[C/T]AGCTCAGGACTGTAA | 55666 |
rs577295541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573241 | TATAGGGCCTTACAT[A/G]AAAGTTTACGTTTAT | 55666 |
rs577295655 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559601 | TTAATGCCCTCAGAA[A/G]AATGCCTCCTGCACC | 55666 |
rs577303236 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578628 | TCACAAGGTGGCAGG[-/A]AAAGAGAAGTGCCGA | 55666 |
rs577303661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579064 | TACCTGGGGCCACAG[A/G]TGCACACAGCATAGA | 55666 |
rs577318834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580026 | ACTCACCAGGGAGCT[C/G]CTTTCTTGCCTGCCT | 55666 |
rs577358360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578263 | GTGCTCTCCAGGTAC[A/G]TAGCTTCAGCAGATT | 55666 |
rs577399219 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629367 | CGACTAATTTTTGTA[A/T]TTTTAGTAGACGGGG | 55666 |
rs577416084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624414 | CAAGAGTGAAACTCC[A/G]TCTCAAAAAAACAAA | 55666 |
rs577478417 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619234 | CACAAAAAATTAGCC[A/G]GGCATGTTGGCGGGC | 55666 |
rs577542896 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81577416 | TCTTCTCCCTCTGAA[A/C]CACAGCTTGGCTCAT | 55666 |
rs577582707 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589566 | CAGTAGTCAACGGAT[C/G]GGTGGCCACAGCACA | 55666 |
rs577641599 | in-del | -/G | 0.0197687 | 0.0974348 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617250 | CAACAGACAGATTTA[-/G]GGGGAAAAAAAATCA | 55666 |
rs577645129 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585820 | GGTGAAATCCTGATT[C/G]TACTAAAAATACAAA | 55666 |
rs577669831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619371 | AACACAGTGAGACTC[C/T]GTCTCAAAAAACAAA | 55666 |
rs577674242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623409 | GGTAGAGGCTGCAGT[A/G]AGTCGAGATCATGCC | 55666 |
rs577712823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638918 | ATAATTTCTAATCTT[A/G]TGGCTAATTTGTTAG | 55666 |
rs577772267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633482 | TCCAGGTTTCCAAGG[C/T]CAACTCCAGTATTTA | 55666 |
rs577779844 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580221 | CTCTCCCAAGCAATG[C/T]GCTCACCCCGGGTGG | 55666 |
rs577826496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608130 | ACTACTGTGGTACCA[C/T]GAGGATTAGTGGCTG | 55666 |
rs577869232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568559 | CAGCAAATCGGACCT[G/T]GCCTGATCTGCCAGT | 55666 |
rs577870508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568225 | TCTGACTTTTCCTGT[C/T]GAGCTGTATTCTCCA | 55666 |
rs577952299 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612011 | ATAACAAAGCTGGTA[C/T]GTGAACATGGCAAAG | 55666 |
rs577988470 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557466 | ATAATAGCGTGGTGG[-/A]TAAGGACGAGCGAGT | 55666 |
rs577995332 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634470 | AAATGGCCTTGTCTG[A/T]AACACTTTTCACTTG | 55666 |
rs578002451 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605929 | AGGTTCAAGTGATTC[C/T]CCTGCCTCAGCCTCC | 55666 |
rs578031355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81566555 | GACTAGGGAAGGCAC[A/G]GGCAGGGAAGAGGCA | 55666 |
rs578051077 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571884 | CTGGGTGCCTGTTCT[C/G]GGGTGGGCACTGCTC | 55666 |
rs578135995 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561237 | GCTGGGATTACAGGC[A/G]TGAGCTACCATGCCC | 55666 |
rs578153837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572449 | ACCCGCCTCAGCCCC[A/C]CAAAGTGCTGGGATT | 55666 |
rs578174052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627751 | CCAGCCTGGGCAACA[A/G]GAGCGAAACTCTGTC | 55666 |
rs578188683 | snp | C/G/T | 0.000944944 | 0.0217161 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81569036 | TCTCACCCAATACAT[C/G/T]CCGGTTTTCAATAGG | 55666 |
rs578212000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627346 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCATTCC | 55666 |
rs578213565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562078 | ATCTCTACTAAAAAT[A/G]TAAAAATTAGCCAGG | 55666 |
rs745311068 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557928 | TCTCTGTTCATAGTG[C/T]CAAGAATGTGGGTCA | 55666 |
rs745333725 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629045 | ACCACACCCGGCTAA[-/T]TTTTTTGTATTTTTA | 55666 |
rs745334734 | snp | C/G | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637806 | GGGCGTGGTGGCGGG[C/G]ACCTGTAATCCCAGC | 55666 |
rs745376381 | snp | A/G/T | 0.000115944 | 0.0076132 | stop-gained, synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622234 | CTTGTTTCTATTGAT[A/G/T]TAAACCGAGAAGCCA | 55666 |
rs745452863 | snp | C/G | 1.65897e-05 | 0.00288003 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622133 | GGACCTCATTTCCCC[C/G]CATTCCCTGCTTCCT | 55666 |
rs745473178 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582470 | ACAGTGGTACAATCA[G/T]AGCTCACTGCAGCCG | 55666 |
rs745531870 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624890 | CCAGAGGCCAATAAA[C/T]AATAAGGAAGATGGA | 55666 |
rs745630952 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579664 | CTGTCCCTGACACAC[A/G]GACCATGCCCCTTCC | 55666 |
rs745648236 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585031 | AAAAATCAGCCAGGC[A/G]TGGCAGCGTGCGCCT | 55666 |
rs745664021 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598621 | AAACCTGTGACCCAG[C/G]AACCCCTGCACGTTC | 55666 |
rs745676071 | snp | A/G | 1.66313e-05 | 0.00288364 | synonymous-codon, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81588977 | CACGTACTGCTCACT[A/G]CTAGACTCCTTGGCG | 55666 |
rs745718236 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600156 | TAAGTCAGAGGAACA[C/T]AAAGGTTATTGGTGC | 55666 |
rs745724901 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620316 | GCTTGGCCAACTTAG[C/T]GAAACCCCACCTCTA | 55666 |
rs745734679 | snp | A/G | 1.94619e-05 | 0.00311938 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606819 | CAAACTTCCCCCTAC[A/G]TAGAAGAGAAGCAAC | 55666 |
rs745738707 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604267 | ACACTACAGAGTCAA[C/T]GAGCAAACCTGGACA | 55666 |
rs745791594 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560361 | AAGCCTGCAGTGAGC[C/T]GAGACCCTGCCTCTT | 55666 |
rs745792713 | in-del | -/AC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602924 | TATATGTATATATAC[-/AC]ACACACACATATATA | 55666 |
rs745814942 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632382 | CAATGGCGTGATCTC[A/G]GCTCACTGCAACCTC | 55666 |
rs745816352 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566264 | TTGAACCCAGAAGGC[A/G]GAGGTTGCAGTAAGC | 55666 |
rs745824625 | snp | C/T | 1.66048e-05 | 0.00288134 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606708 | GTCTGTTCAGCGTGA[C/T]GGCGCTCGGCTGGCA | 55666 |
rs745826311 | snp | A/C | 0.000192623 | 0.00981194 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637440 | TCAGGAAGGCAGGAT[A/C]ACACCTTCATGTTTT | 55666 |
rs745844633 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576307 | AGAATTACAGTTGGC[C/T]GTTGCACAACGCGGG | 55666 |
rs745912153 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636798 | GAGAAAGCCCTGGCG[A/G]GAGAAGAGAAAGGGG | 55666 |
rs745912612 | snp | C/T | 1.658e-05 | 0.00287919 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629853 | AGCCTAGTGAGGTCC[C/T]GATCTAATACTACGG | 55666 |
rs745936307 | snp | C/T | 1.75299e-05 | 0.00296051 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81565548 | CTCAGACCTCTTCCA[C/T]GTCTGGGCGAGCTCC | 55666 |
rs745985101 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571581 | GCAGCTGTGCTGGGG[A/C]TAGGGCAAGCACCTG | 55666 |
rs745996302 | in-del | -/GTCAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570844 | CCTCACTTCCACAGG[-/GTCAA]GGAGCCTGGGCATCA | 55666 |
rs746015624 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622521 | AAACTTTGTAAAACA[C/T]TTAAGACTTTGAAGC | 55666 |
rs746026283 | snp | C/T | 8.30158e-05 | 0.00644213 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597357 | AACATCTCCTCAAGA[C/T]AGACGATGAATGGCT | 55666 |
rs746040858 | snp | A/G | 0.000150841 | 0.00868319 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565325 | GTCTGCTCCATCACC[A/G]GAGCCTGCCACGTGC | 55666 |
rs746078041 | in-del | -/TC | | | frameshift-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81629750 | AATGTTGCTGCTGTT[-/TC]TCTCTTTGTTGCTGT | 55666 |
rs746078395 | snp | A/G | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556645 | GAGGCACCCAAGGGC[A/G]GCGGGGCCGTCAAAC | 55666 |
rs746102128 | in-del | -/GGC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576649 | AAAGAACGAAAACCT[-/GGC]GTGTGTTTGCAACAC | 55666 |
rs746128172 | snp | C/G | 1.65644e-05 | 0.00287783 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613383 | CTGATCAATCTCATC[C/G]TCCACCACGTTGGGA | 55666 |
rs746137089 | snp | C/T | 1.65669e-05 | 0.00287805 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597240 | CAGTCCTGTCTCCAC[C/T]TCACCTTATTTCGAC | 55666 |
rs746160400 | snp | C/T | | | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81564193 | CAATCATACCCCAAC[C/T]TCAGCATCAGGCAAT | 55666 |
rs746210652 | snp | C/T | 3.36746e-05 | 0.00410319 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613282 | ACCCATTAAGATCAC[C/T]ACAAGTAGGACCCTG | 55666 |
rs746215143 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615966 | TTAACTCAAAGGAGT[C/T]GTAGGTCCATCACAC | 55666 |
rs746303104 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614087 | CAAGACCATCCTGGC[C/G]AACAGGGTGAAATCT | 55666 |
rs746355186 | in-del | -/AAAG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607407 | ACAAAAAAAAAAAAA[-/AAAG]AAATCTGTATCTTTA | 55666 |
rs746381373 | snp | A/C | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562636 | CCAGTCAGAACTTAC[A/C]CCAGTCAGAACTGCC | 55666 |
rs746394987 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588660 | GGACCCATCTTCTCA[C/T]CTTTAGAAACTGAGA | 55666 |
rs746562303 | in-del | -/AA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633131 | GACTCCGTCTCAAAA[-/AA]AAAAAAAAAAAAAGA | 55666 |
rs746587407 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619304 | ATGGCATGAACCCGG[C/G]AGGTGGAGCTTGCAG | 55666 |
rs746612099 | snp | A/C | 1.69132e-05 | 0.00290797 | missense, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81588952 | CTTTTACCTTATAAA[A/C]CACATCAGGCACGTA | 55666 |
rs746617172 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583788 | CTCCCTCCTGAAGGA[C/G]AGTCAGGAAGCTTCT | 55666 |
rs746687235 | snp | C/G | 1.68661e-05 | 0.00290392 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606768 | GGTGCCCCTCGCACC[C/G]TGACTTAATCTTGCA | 55666 |
rs746701777 | snp | A/G | 2.06188e-05 | 0.00321076 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572104 | CTGCAATAGTCAGAG[A/G]GGAACAGCGGTGAGC | 55666 |
rs746777152 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577314 | CACTGTCCCTTGGCA[C/G]CAGGACATCACCCTC | 55666 |
rs746814719 | snp | G/T | 1.6666e-05 | 0.00288664 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606685 | GACAGACAGGGAACA[G/T]CTCACCTGTCTGTTC | 55666 |
rs746817003 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586667 | GGATACCTACATATT[C/T]AAGCTGTATGAGGCA | 55666 |
rs746854861 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607020 | CCAGCTTCTGTCCCA[A/C]ATACTTCAACCATAC | 55666 |
rs746859051 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632516 | ATGGGATTTCACCAC[A/G]TTGGCCAGGCTGGTC | 55666 |
rs746927334 | snp | C/T | 0.000261952 | 0.0114415 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565480 | CCAGCCACGGGGTGC[C/T]GGGGCAGGGGGTGGG | 55666 |
rs746950565 | snp | C/T | 3.31252e-05 | 0.00406958 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81629737 | TACCTTTTTCAAAAA[C/T]GTTGCTGCTGTTTCT | 55666 |
rs746967534 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621281 | GTAGGTGCCCAATAC[A/C]TCTTTGTTAAGAACA | 55666 |
rs747089430 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597672 | CCTGTAATCCCAGCT[A/C]CTCAGGAGGCTGAGG | 55666 |
rs747120316 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587860 | TTTTTTTTTTTTAGT[A/G]GAGACGGGGTTTCAC | 55666 |
rs747159588 | snp | C/T | 8.42609e-05 | 0.00649025 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613272 | CCCTTTATTCACCCA[C/T]TAAGATCACCACAAG | 55666 |
rs747165780 | snp | A/C | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567608 | ACAGAGCTGTTTCCT[A/C]CTAAGACGCAACTCA | 55666 |
rs747178868 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599872 | ATGATTGATGACGGA[A/G]CAGCAGAAGCTCCAA | 55666 |
rs747197544 | snp | C/T | 1.65658e-05 | 0.00287795 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596209 | GGAAGTCTCCTGCAG[C/T]GATGCACTCTTCTGA | 55666 |
rs747249406 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631114 | GGAGGCAGAGGTTGC[A/C]GTGAGCCAAGATCGT | 55666 |
rs747256896 | in-del | -/AAAAGAAAAAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621130 | AGGAAGGAAGGAAAG[-/AAAAGAAAAAA]AAAAGAAAAATATCA | 55666 |
rs747262029 | in-del | -/AA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585674 | TCTGGGGGGGGGGGG[-/AA]AGAAAGAAATCAGAG | 55666 |
rs747273762 | snp | C/G | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556810 | ATATCTTGGAGACAA[C/G]TTATCAAATCCCCCC | 55666 |
rs747296132 | snp | C/T | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636344 | AGAGGAATTGTCAAG[C/T]TGTCCTTCCAAGTAA | 55666 |
rs747324844 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603932 | ATATAAATATACACA[C/T]ACAGCCCAATTCCCA | 55666 |
rs747366036 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589644 | ACACACTTGGCTCCA[A/C]AAACAGGTGCCACTA | 55666 |
rs747381149 | snp | C/T | 1.67536e-05 | 0.00289423 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569116 | GTTGTTGTGATCTAA[C/T]GAAGAAAAACACAAA | 55666 |
rs747404714 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558454 | AGGCACTGAGGTTTA[C/T]TTCAAGGGAGAACTG | 55666 |
rs747426647 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557773 | CCACAATAGCTCTGC[C/T]GTGACCAGACCCAAC | 55666 |
rs747449755 | in-del | -/CC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574881 | AAACAAACAAACACA[-/CC]CACACACACACACAC | 55666 |
rs747469570 | snp | C/T | 1.69249e-05 | 0.00290898 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568969 | ACTGACACTAGATAA[C/T]AATCAGCAGTTACCT | 55666 |
rs747536222 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567399 | TTGCTCAAGTGGACA[C/G]CACACTTGGACACGC | 55666 |
rs747560469 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580622 | GAGCTGCTCTGCCAA[C/T]TGACACCTTCTCTCC | 55666 |
rs747560554 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591003 | TAATATCTCAGCAAA[A/G]ATACAGGCACCTCAC | 55666 |
rs747583677 | in-del | -/AGAC | 1.67624e-05 | 0.00289498 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606669 | CATGAAAACAAATCT[-/AGAC]AGACAGGGAACATCT | 55666 |
rs747712299 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627958 | GAAATTTGTATTGAA[C/T]GAAAATATCCTTGGG | 55666 |
rs747737505 | snp | A/G | 1.67742e-05 | 0.002896 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606664 | TCAGCCATGAAAACA[A/G]ATCTAGACAGACAGG | 55666 |
rs747745588 | snp | A/G | 1.69815e-05 | 0.00291384 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569144 | AAACCCATGATAAAT[A/G]AGGCTGAAAATGGTG | 55666 |
rs747757257 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576057 | CAACAAAGGAATAGA[C/T]TGTAGGTAAGTGGCA | 55666 |
rs747809011 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596546 | ACTCCAACCTGTGCA[A/G]CACAGCAAGACTCTG | 55666 |
rs747831924 | snp | A/G | 7.11769e-05 | 0.00596518 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604686 | AAAGCGGTCAGCGAC[A/G]GTGTGATTCTCAAAC | 55666 |
rs747849552 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619372 | ACACAGTGAGACTCC[A/G]TCTCAAAAAACAAAA | 55666 |
rs747861645 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616045 | AAATCTGGGCCGGGC[A/G]TGGTGGCTCACGCCT | 55666 |
rs747920116 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569275 | TTATCTATTAGTGTC[A/G]TCTCTAAACGAACAC | 55666 |
rs747936577 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607225 | AGTACTTAGATATTT[A/G]TAAAAAATTCTTATT | 55666 |
rs747940587 | in-del | -/CA | 2.09751e-05 | 0.00323838 | splice-acceptor-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567533 | CAAGCTATGGAAGTC[-/CA]CTAGAGGAATGGGAA | 55666 |
rs747945294 | snp | C/T | 9.94332e-05 | 0.0070503 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629707 | TATCCTGAGGGTCAA[C/T]ACCCAGGCCACAGAT | 55666 |
rs747974970 | snp | A/G | | | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596237 | TGAACTTAGGAAATA[A/G]GTGTCCTAAGACAAG | 55666 |
rs747976912 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585167 | AGAACGAGACTCTGT[C/T]GCCAAAAAAAAAAAA | 55666 |
rs748031448 | snp | A/C/G | 6.95085e-05 | 0.00589493 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559400 | ATGGAGACCTGGGAG[A/C/G]TGCCCGCCAACTGTG | 55666 |
rs748056196 | in-del | -/CTC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575326 | CAGGATGGTCTCGAT[-/CTC]CTGACCTCATGATCC | 55666 |
rs748057863 | in-del | -/TAA | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635357 | AAAATAAAATAAGGT[-/TAA]AAAAAAAAAAAAAAA | 55666 |
rs748061522 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583296 | ACCAAAGGCCATCAA[C/G]ACAAGACCAATTAAA | 55666 |
rs748124485 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608084 | CTGGCCACTGTTACC[A/G]CCTCTGCCCACCTGG | 55666 |
rs748149346 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583850 | GTATGTCCACATCCA[C/T]GTGCAAATGCCTATA | 55666 |
rs748269043 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578465 | ACAGATAAACGGTAC[A/G]ACTGGTCCGTTTTCT | 55666 |
rs748297218 | in-del | -/ACACAC/ACACACACAC | | | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81564085 | GCTCCAGCTCAAAAC[-/ACACAC/ACACACACAC]ACACACACACACACA | 55666 |
rs748319888 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588242 | AACTTCAGGCAGCCA[A/G]ATACATGTGTAACTG | 55666 |
rs748328198 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633681 | GAAGTTGAAGAACTG[A/G]TGAGATACAGTTAAA | 55666 |
rs748343326 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618342 | GGAGCGCCTCTGCCT[C/G]GCCGCGACCCCGTCT | 55666 |
rs748345602 | snp | C/T | 0.000101112 | 0.00710956 | missense, intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81608756 | CAGTCAGCTTCCGGA[C/T]GTAGGCGTGGAAGGA | 55666 |
rs748350857 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590202 | ACTCCACGGCCGTGG[C/G]CAGACCTGGGAGCCC | 55666 |
rs748398184 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620657 | CTGAGGTGTTCAGTA[C/T]GTATTTTGTTTAATA | 55666 |
rs748407589 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586879 | GCAACTCGGCTCTGA[C/T]CAGCTACTTGCCACC | 55666 |
rs748421488 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569548 | AAGAGAGATTCGTGT[C/T]ATTGGATTCGGAGGG | 55666 |
rs748459163 | snp | A/G | 0.000161541 | 0.00898578 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567447 | TTCATTGGTGACCAG[A/G]AACAGCAAGAGGTGG | 55666 |
rs748502331 | in-del | -/GGC | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559007 | TTGTCAACAGGATTA[-/GGC]GGCGTGAGGAGCCGC | 55666 |
rs748509596 | snp | A/G | 1.98379e-05 | 0.00314938 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604515 | CAGCCTCCAAACACA[A/G]AAACTCAGGAACTTG | 55666 |
rs748578228 | snp | A/C | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637775 | CCCGTCTCTACTAAA[A/C]ATACAAAAATTAACT | 55666 |
rs748581562 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611180 | CAAAAATTAGCCGGA[C/T]GTGGTGGCAAGCACC | 55666 |
rs748589667 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598885 | TTAAAGATGCCCCAA[C/T]GAATGAAAAACCCAA | 55666 |
rs748597467 | snp | A/C | 2.01794e-05 | 0.00317636 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81600365 | GCCAAGTTTGGCAGC[A/C]ATTTCATCGACCACT | 55666 |
rs748667383 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632177 | GACGGGGTTTCAACA[C/T]GTTAGTCAATCTGGT | 55666 |
rs748675478 | snp | A/C | 1.65985e-05 | 0.00288079 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622125 | GATCATGGGGACCTC[A/C]TTTCCCCCCATTCCC | 55666 |
rs748685469 | snp | A/G | 3.68861e-05 | 0.00429438 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600304 | GCCCAACAGAGCCTG[A/G]CCACGCCCCCTGCTT | 55666 |
rs748699609 | in-del | -/GAGT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564443 | CCAGCCTCGGCAATA[-/GAGT]GAGACCCTGTCTCTA | 55666 |
rs748700437 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634008 | GGCTGGGACTACAGG[C/T]GCACGCCACCACGCC | 55666 |
rs748715776 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625678 | TAAGGCTACAATGAG[A/G]TATGATCACACCACT | 55666 |
rs748749457 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576167 | AGGCAAACATCTAGA[A/G]AAGCACAAAAGCTAG | 55666 |
rs748785154 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611583 | TCAAACTCCTGACCT[C/T]AGGTGATCCACCTGC | 55666 |
rs748814067 | snp | A/G | 1.76045e-05 | 0.00296681 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604676 | AGAAGTCAAGAAAGC[A/G]GTCAGCGACGGTGTG | 55666 |
rs748821067 | snp | A/G | 1.82277e-05 | 0.00301886 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604542 | CTTGAATCCCGTCAT[A/G]TTTACCTGAGGTGGC | 55666 |
rs748847455 | in-del | -/AG | 1.66283e-05 | 0.00288338 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569007 | TGTTTCTAAAGACAA[-/AG]AGCTCACCTGTGTCT | 55666 |
rs748867675 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630734 | AAATACAAGTTAGCC[A/C]GGCATGGTGGCGTAC | 55666 |
rs748884805 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559113 | TGCTGAGAAGCTTCA[A/G]TGGGTCAGGGAGCCC | 55666 |
rs748941511 | snp | A/G | 1.65468e-05 | 0.00287631 | missense, nc-transcript-variant, stop-gained | NPLOC4 | GRCh38.p7 | 17:81559395 | TACTCATGGAGACCT[A/G]GGAGCTGCCCGCCAA | 55666 |
rs748997634 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603994 | TGGCATAATCATACC[A/G]AGAGGGCCTTCCAAT | 55666 |
rs749014914 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598024 | GGTGTGAACCCGGGA[A/G]GTGAAGCTTGCAGTG | 55666 |
rs749081848 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596527 | GCCGAGATTGTGCCA[C/T]TGCACTCCAACCTGT | 55666 |
rs749100852 | snp | C/T | 4.95442e-05 | 0.00497691 | missense, nc-transcript-variant, synonymous-codon | NPLOC4 | GRCh38.p7 | 17:81559366 | CCGTGTGTGTGGAGC[C/T]CCCGACGGCGCCGTA | 55666 |
rs749124693 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569165 | GAAAATGGTGTGGCC[A/G]ACTCCCAGCCAGCCC | 55666 |
rs749146451 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622305 | CCCAAAGAACAGAAA[C/T]TTAATGAAATGCTAA | 55666 |
rs749151316 | in-del | -/CA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621836 | AACATGATTTCCCGG[-/CA]CACAGCTGTGTTCAA | 55666 |
rs749162956 | snp | A/G | 5.93971e-05 | 0.00544931 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589142 | AAGAGTCTACCAAAC[A/G]GCATTCAAAACCAGT | 55666 |
rs749248661 | snp | C/G | 1.66693e-05 | 0.00288693 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608715 | CACAACCAGGTTACA[C/G]CAAGTTGCTTACTTG | 55666 |
rs749277834 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597395 | GTGACTCACGCCTAT[A/C]ATCACAGCACTTTGA | 55666 |
rs749286555 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583967 | TTATCTTTAAATAAT[C/T]TGCAAACACATACCT | 55666 |
rs749379595 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588546 | AGAGACACAGTCTCG[C/T]TATGTTGCCCAGGCT | 55666 |
rs749400380 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608176 | CTGAAAACCAAGCTG[A/T]CTCAGAGGCCAGGCT | 55666 |
rs749414538 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81556984 | GAGCCGAAACAGAGC[C/T]GAAGCAGGAGCACCT | 55666 |
rs749438018 | in-del | -/CAC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586914 | TGGAGATGGACAGCT[-/CAC]CACCACCACATTTCC | 55666 |
rs749468703 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580262 | CTAGCACATCGCCGA[A/C]AGATCCCCAGCCTTC | 55666 |
rs749556996 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579801 | CCCACTTCCCATACT[A/G]GTGACTGTCCTTTGC | 55666 |
rs749562075 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574204 | AAATCTAATTAAGCT[C/T]TAATATGCAGAAACA | 55666 |
rs749600820 | snp | A/C | 3.78179e-05 | 0.00434828 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600291 | CCCTGGCCTGGATGC[A/C]CAACAGAGCCTGGCC | 55666 |
rs749614164 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583052 | TGCCACGTGACGCAG[A/G]GTGTGTGTGACACAC | 55666 |
rs749666974 | in-del | -/ATT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573118 | GAACCAAAGCTTTTC[-/ATT]AAAGATTCTGCAAGA | 55666 |
rs749674504 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608127 | GCAACTACTGTGGTA[-/C]CATGAGGATTAGTGG | 55666 |
rs749708379 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562453 | CAGAGGCTGGACAAT[A/G]GCTTGAACCCGGGAG | 55666 |
rs749739377 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625902 | GCCTGTAATCCCAAC[A/G]CTTTGGGAGGCCGAG | 55666 |
rs749744553 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558874 | GGGGGCAGGGAGGCC[-/A]AACAAAAAGCACTGA | 55666 |
rs749766076 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613076 | CTTTGTACCCAAATG[C/T]TTCAAAATTTTTTAT | 55666 |
rs749771374 | in-del | -/GGGAAGCCTGCA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560343 | CCATGAACCCGGGAG[-/GGGAAGCCTGCA]GTGAGCCGAGACCCT | 55666 |
rs749807551 | in-del | -/TTTCT/TTTCTT/TTTT | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615100 | AGAGACGTCTGTTTC[-/TTTCT/TTTCTT/TTTT]TTTTTTTTTTTTTTT | 55666 |
rs749834532 | snp | A/G | 1.67458e-05 | 0.00289355 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613298 | ACAAGTAGGACCCTG[A/G]AATCTCATGGATCAC | 55666 |
rs749841641 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614066 | TGGATCACAAGGTCA[A/G]AAGATCAAGACCATC | 55666 |
rs749883837 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563262 | GTAGTTTTAACAGAA[A/G]TGGGGTTTCACCATG | 55666 |
rs749902370 | snp | G/T | 1.66446e-05 | 0.00288479 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596283 | AATTTTACAGCATCA[G/T]GCCAAAATATACTTC | 55666 |
rs749930800 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568965 | CAATACTGACACTAG[A/G]TAACAATCAGCAGTT | 55666 |
rs749950444 | snp | A/G | 2.26431e-05 | 0.00336468 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559389 | GCGCCGTACTCATGG[A/G]GACCTGGGAGCTGCC | 55666 |
rs749960187 | snp | A/C | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578236 | CTAGACTGGCCCCGC[A/C]GGGTGCATGCTGTGC | 55666 |
rs750009973 | in-del | -/A | | | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563888 | TACATGTTTTCATTT[-/A]TAAGTGGGAGCTAAA | 55666 |
rs750040060 | snp | A/G | 1.65641e-05 | 0.00287781 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596165 | ATGTCCGTCTGGAGA[A/G]AGCCGGCACATGTTG | 55666 |
rs750075503 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621897 | ATGCAGCTCACTCCA[C/T]GCCGTACATGGACAA | 55666 |
rs750118402 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573542 | TTAACAGTCAGTTAC[A/G]GATCCAACTCCTTGT | 55666 |
rs750200015 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582856 | GGCTCTGGGGCTGCA[C/T]ATAAAGCTCCACAGC | 55666 |
rs750219063 | snp | A/G | 0.000153539 | 0.00876048 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608699 | CAAAAAGGAATTTAC[A/G]CACAACCAGGTTACA | 55666 |
rs750239406 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562167 | AACCCAGGACGTGGA[A/G]GTTGCAGTAAGTGGA | 55666 |
rs750240120 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623434 | CATGCCACTGCACTC[C/T]AGCCTGGGTGACAGA | 55666 |
rs750330456 | snp | C/T | | | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81600372 | TTGGCAGCAATTTCA[C/T]CGACCACTTCAGCTT | 55666 |
rs750360983 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572473 | TGGGATTACAGGCGT[A/G]AGCCACCGCGTCCGG | 55666 |
rs750432346 | snp | A/G | 4.96841e-05 | 0.00498393 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600453 | TCAAAGGGAGAAGAT[A/G]GACTTAGAGCAGAGG | 55666 |
rs750437356 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632915 | TGTTCTCAACTTTTA[A/T]GTCAGGAGATTGAGA | 55666 |
rs750505055 | snp | C/T | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622166 | TCAGAGGACACTTAC[C/T]TGATTTTTAGCAAGT | 55666 |
rs750523984 | snp | A/T | 2.84386e-05 | 0.00377074 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600330 | TGCTTGGCTGCCGGA[A/T]GCCTCAGTACCTTCC | 55666 |
rs750529964 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558166 | TGCTGTTCCAGATCG[C/T]CCAGTCTCCCTCTAT | 55666 |
rs750547041 | snp | A/C | 6.69785e-05 | 0.0057866 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613508 | GCCTGTTCAAATGAT[A/C]AACAGAGGCTGATGC | 55666 |
rs750589857 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566187 | AAATACAACAATTAG[A/C]CAGGCGTGGTTGCGG | 55666 |
rs750592994 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612096 | CATTTTGGGAAATAA[A/C]AACAATGAAAAAACC | 55666 |
rs750619887 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582079 | GGCCCAGACACCACA[A/G]TGAATCACCAGAAAA | 55666 |
rs750665584 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624555 | GTGAGATGAGATCAC[A/G]CCATTACACTCTAGC | 55666 |
rs750700616 | snp | A/G | 5.6134e-05 | 0.00529753 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559215 | CTTCTGGCTTCAGGA[A/G]GGGCTGGGCTGGGCC | 55666 |
rs750727239 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575896 | CAGTTTCTTGATTAA[C/T]TGATAAACCTGCCTG | 55666 |
rs750740411 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599570 | TTTGCAGTCTCACCC[-/G]CTTCATCTGTAGAGA | 55666 |
rs750792517 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584628 | AGGGCTGATGATGGA[A/C]AGGATAATACGTGTA | 55666 |
rs750803053 | snp | A/G | 1.7698e-05 | 0.00297468 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588910 | TTCACACCATTCTCC[A/G]TGTACAGAGTTCTTT | 55666 |
rs750829619 | snp | G/T | | | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81565300 | CTAAGACGTACGGCC[G/T]GGACAACATGTCTGC | 55666 |
rs750840540 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619749 | CTGGGAATGGTGGTG[A/G]GCACCTGTAATCCCA | 55666 |
rs750842676 | snp | A/G | 0.0001148 | 0.0075754 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81572068 | CAGCTGGGTGATCTC[A/G]TTGCCAAACTTGTCT | 55666 |
rs750997400 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637244 | TTTGGAAAGTTGCGT[C/T]TGAGATTACTTCTGC | 55666 |
rs751017597 | snp | C/G | 5.71265e-05 | 0.00534416 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636950 | GCTGCTCCTGCCTCC[C/G]GGCTCGAGCCCCGGG | 55666 |
rs751041289 | snp | C/G | 6.26115e-05 | 0.0055948 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608834 | ATGGCTGCCAAGACA[C/G]AGAGTAAGCGAGTGC | 55666 |
rs751047766 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569922 | CAAAGCAGCACCGAG[C/T]TGAGTTGATGCTGCT | 55666 |
rs751093765 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580094 | CTGCCTCCCAGTGCT[C/G]TCCACCTCATTCCCC | 55666 |
rs751098294 | snp | A/G | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638001 | GGATACCAGGAAACC[A/G]GAAGACTAAATGTAT | 55666 |
rs751121560 | snp | A/G | 1.85379e-05 | 0.00304444 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589126 | GAGAGAGACCTTTAA[A/G]AAGAGTCTACCAAAC | 55666 |
rs751127025 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597160 | AAAGCTAGAACCAGC[A/G]GTGCAAAGAGACCCT | 55666 |
rs751146469 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586996 | TCTGGCTTGTGATAC[A/G]CAATGAGCAGCACAC | 55666 |
rs751265697 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595910 | GGTCCTGATTCTGTT[A/G]TGAGTTTTGGGGTTT | 55666 |
rs751281778 | snp | A/T | 2.14498e-05 | 0.00327482 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567536 | AGCTATGGAAGTCCT[A/T]GAGGAATGGGAATAA | 55666 |
rs751366875 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633594 | AGACAGACCTGACAA[C/T]ATGAACACACAGCCT | 55666 |
rs751399546 | in-del | -/ATTAA | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638081 | AAATTACATTAATTG[-/ATTAA]ATTAAATTATGTTAG | 55666 |
rs751411469 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579524 | TCCAGCCTCCCCCTT[A/C]AGCTGACCCTGTGGC | 55666 |
rs751456343 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627282 | CTGTAGTCCCAGCTA[C/G]TCGGGAGGCTGAGGC | 55666 |
rs751492518 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562265 | CCATGAGGGCCGGGC[A/G]CGGTGGCTCACACCT | 55666 |
rs751501403 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588128 | TGAGACACTGTAGAA[A/G]TCCAGATCAACGAAT | 55666 |
rs751543296 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601566 | CTGGCCTCAATTATA[C/T]TTTTAATAGAACCGT | 55666 |
rs751552683 | in-del | -/AA | | | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563589 | AGGGAAACAAAAAAG[-/AA]AAAAAAAAAAAAGAC | 55666 |
rs751561205 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634402 | TCTGAGACATTCAAC[A/G]AGATCCAATGCTGTC | 55666 |
rs751567955 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625499 | AGAACAATCAAATGG[A/C]AATTCTAGAACTGAA | 55666 |
rs751583999 | snp | C/G | 1.68086e-05 | 0.00289896 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613449 | CTCCATTTCAGATGA[C/G]GGCCCAGCAAGGCTC | 55666 |
rs751653037 | snp | C/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638588 | ATAGACGTGAGCCAC[C/T]GTGCCCGGCTGGGGA | 55666 |
rs751653055 | in-del | -/CCCCCTCCCCC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617662 | AAACACAAAAAATGC[-/CCCCCTCCCCC]CCCCCCTCCCCCTCC | 55666 |
rs751682089 | in-del | -/GA | 0.000558191 | 0.0166968 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610264 | GTGGCGGCATCTGAG[-/GA]GAGTACAAGGCAGAA | 55666 |
rs751692497 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593705 | ACCGAGAAGAGTATG[A/C]CGACACTTTTCTCCC | 55666 |
rs751693331 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573786 | GCAGGAGAATGAACC[C/T]GGACTCTATTTCCAT | 55666 |
rs751782727 | in-del | -/ACACACACAG/ACACAG | | | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81564109 | CACACACACACACAC[-/ACACACACAG/ACACAG]ACACACACAAAGAGC | 55666 |
rs751834354 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626702 | AGCTAGGAAGCTCAC[A/G]TGGGAGGATCGTTTG | 55666 |
rs751874662 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631945 | GCTGGAATCACAGGC[A/G]CCCACCACCATACCC | 55666 |
rs751944710 | snp | A/G | 1.68247e-05 | 0.00290035 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606644 | CTTCTGGAAATATCC[A/G]TTTCTCAGCCATGAA | 55666 |
rs751946257 | snp | A/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567219 | TGAAAAAATTAATCT[A/T]TCTATCAACAAGCTT | 55666 |
rs752040425 | snp | C/T | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81629802 | GGGACTGGACACGAA[C/T]TATCTGTTGCAAACA | 55666 |
rs752051895 | snp | A/C | 1.65861e-05 | 0.00287972 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629679 | GATGGCAGTAAGAGT[A/C]GAGGATGAAAAATAT | 55666 |
rs752060168 | snp | A/C | 3.94019e-05 | 0.0044384 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559464 | TTTCTGGCCCACCAG[A/C]GACTGCCAGAGTGTG | 55666 |
rs752144592 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604855 | ACCAATAGGGTGTGA[C/T]GGTGCATGCCTGTGG | 55666 |
rs752168441 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560805 | GTTCTCGCGAGGGTG[A/G]CACGGTTTTGCCTCC | 55666 |
rs752218314 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624963 | CACAGACGAAAGGCA[A/G]GGGGAATCATCATCC | 55666 |
rs752225162 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599795 | CTCATCTTCTAACTG[A/T]TCCATGAAACTAGGA | 55666 |
rs752326409 | snp | C/T | 7.18184e-05 | 0.005992 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636967 | GCTCGAGCCCCGGGC[C/T]GCCGCCGCCTGCCGC | 55666 |
rs752338044 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598478 | GTCTTTCCTGACAAG[C/T]TAAGAAAAAGGATTC | 55666 |
rs752340097 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589222 | AAGAGTTTGTCGGGG[A/G]TAAGAGTTAAAAAAT | 55666 |
rs752492142 | snp | A/G | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638487 | ATTTTTCGTAGAGAC[A/G]GAGTTTCTCCATGTT | 55666 |
rs752523444 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622072 | CCATAATGAGTGGTG[C/T]GATGAGGAAAGAGGA | 55666 |
rs752627679 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624343 | GAATTGCTTGAAACC[A/G]GAAGGCAGAGGTTGC | 55666 |
rs752631220 | snp | A/C | 1.65748e-05 | 0.00287874 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597218 | CCAAGCCATAGGGCC[A/C]CACGCACAGTCCTGT | 55666 |
rs752632449 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580181 | AGGCCTCAAGCACCA[A/C]CCCAACACCATCTGT | 55666 |
rs752644430 | in-del | -/AG | 2.28799e-05 | 0.00338222 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613512 | GTTCAAATGATAAAC[-/AG]AGGCTGATGCCTTCC | 55666 |
rs752644522 | in-del | -/A | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556450 | TCTGTTGTCACAGGG[-/A]AAGACAGCTCAAGCA | 55666 |
rs752684846 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590284 | AGTCTCCACTCCATC[A/G]AAGCCTCCAGAATGA | 55666 |
rs752717621 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623025 | CATGGTGAATCCCCG[G/T]TTCTACTAAAACTAC | 55666 |
rs752728758 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583547 | GGCTGCCCCAGAGAT[C/G]AGTGAGGCTGGCTGG | 55666 |
rs752728948 | snp | C/G | 0.000149835 | 0.0086542 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610286 | CAAGGCAGAAAAAGG[C/G]AGAGCAGTGAGGATG | 55666 |
rs752814003 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628463 | GGTTGCAGTGAGCCG[A/C]GATCATGCCACTGCA | 55666 |
rs752826507 | snp | C/T | 6.63823e-05 | 0.00576079 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81569064 | AGGAAATGGATTTTG[C/T]GAAATAGAAAAAGTG | 55666 |
rs752850489 | snp | A/C | | | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563953 | AGGTGTGGTGGTACA[A/C]ATCTGTAATCCCAGC | 55666 |
rs752857994 | in-del | -/TATATATACACACACACATA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602916 | ACATACATATATATG[-/TATATATACACACACACATA]TATATATACACACAC | 55666 |
rs752860484 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616708 | GCCCTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 55666 |
rs752866713 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602077 | GAATGTGCGTGCATG[C/T]ATGCGTGTGTGTATG | 55666 |
rs752879006 | snp | C/T | 2.44855e-05 | 0.00349888 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604762 | GGGCTGATGAAAACA[C/T]GCCATCAAAAAGAAA | 55666 |
rs752952605 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600707 | GCACTCAGGACTAAG[A/G]CAAGGCAAGGTCTAC | 55666 |
rs752957155 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573937 | CTCCTTCCACGTGAC[C/G]AGTGGCTGCCAGTCA | 55666 |
rs753002810 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615513 | ATACTCTAAAATCAA[C/T]TGATGAGCTCTAAAG | 55666 |
rs753018216 | in-del | -/AAAC | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562540 | CAAGACTTTGTCTCA[-/AAAC]AAACAAACAAAAAAC | 55666 |
rs753046286 | snp | A/G | 1.67407e-05 | 0.00289311 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622319 | ATTTAATGAAATGCT[A/G]AAGTATCACTACACA | 55666 |
rs753054835 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606594 | ACTGAAAATCCACCA[C/T]GCATAGTGCTAATAG | 55666 |
rs753079136 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558746 | TGTCCAGGGCCACTG[C/T]GTCCCCACCAGACAA | 55666 |
rs753083766 | snp | A/G | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638717 | CTCTTGTGCTGAGTC[A/G]GTTCCTGGGTGGGGG | 55666 |
rs753102492 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595630 | GCTCACTGCAACCTC[C/T]GCCTGATGGGTTCAA | 55666 |
rs753123382 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579100 | TGCATTACTGTTTAG[C/T]GTGGTGGCTCACGCC | 55666 |
rs753127351 | snp | C/T | 0.00036748 | 0.0135501 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567555 | GAATGGGAATAAACA[C/T]GAATGTTCCATACAG | 55666 |
rs753134239 | snp | C/T | 3.31274e-05 | 0.00406972 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622229 | CCGGTCTTGTTTCTA[C/T]TGATGTAAACCGAGA | 55666 |
rs753198260 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581204 | AAAATACAAAAAAAT[G/T]AGCCAGGCATGGTGG | 55666 |
rs753205478 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582986 | CCTCCCTGCGGCGCC[A/G]CCCCTGCGCACTCAC | 55666 |
rs753212690 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632151 | CAGCTAATTTTTGTA[-/T]TTTTAGTAGAGACGG | 55666 |
rs753250769 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607682 | GTGTTCCTTGACCTA[C/G]ACTGAGAAAGGCTGA | 55666 |
rs753293094 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593877 | CCTTCCCAGGGTGCC[C/T]TAACAGGTTCTGTAA | 55666 |
rs753318257 | snp | C/T | 8.31912e-05 | 0.00644893 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559326 | ATGAACGTGCAGTGC[C/T]GACAGGCCCACATGG | 55666 |
rs753361663 | snp | A/C | 0.000736323 | 0.0191734 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565424 | GAATCCAGGGCACCA[A/C]CGGCAGTGGGGAGCT | 55666 |
rs753369056 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632116 | GAGCAGCTGGGATTA[C/T]AGGCGTGCACCACCA | 55666 |
rs753374808 | in-del | -/TTGGCCG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573449 | GCCCCAGGCCCCCAT[-/TTGGCCG]TTGGCCCTTGGCCCT | 55666 |
rs753396977 | snp | A/C | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578127 | CTTCCCGCCTCCAGA[A/C]CACCCCTCCTGACAC | 55666 |
rs753430972 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626738 | GGGAAGTCAAGGCTG[C/T]AGTGAGCTGTGACTT | 55666 |
rs753466351 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633028 | CCAGCTACTTGGGAG[A/G]CTGAGGTAGGAGAAT | 55666 |
rs753470415 | in-del | -/TCAT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573181 | TTAACATTATATAAA[-/TCAT]TCATTAAGTCATATA | 55666 |
rs753499372 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562057 | TGACCAACATGGTGA[A/G]ACCCCATCTCTACTA | 55666 |
rs753503693 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560865 | TTCACATCTTCACTC[A/G]CACTTGACATTGTCG | 55666 |
rs753534208 | in-del | -/T | 1.65655e-05 | 0.00287793 | frameshift-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622253 | ACCGAGAAGCCATTA[-/T]TTTGGAAGCCAAACT | 55666 |
rs753596472 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586347 | CTTTGGGTGGCCTCA[C/T]GCCTATAATCCCAAC | 55666 |
rs753603986 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560070 | AACAAAGTTGCCAGG[A/G]TCATTCTTCTACAAT | 55666 |
rs753638423 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581144 | GACCTGAGGTCAGGA[A/G]TTTGAGACCAGCCTG | 55666 |
rs753644450 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81639102 | GAAGCAAGATGGGTT[-/C]AGTTAAGTCCGATCT | 55666 |
rs753661616 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572249 | GCTGGAATGCAGTGG[C/T]GTGATCTCCACTCAC | 55666 |
rs753710722 | snp | C/T | 7.81097e-05 | 0.0062489 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608864 | CAGTCTCACACGTGC[C/T]GGTCACTCCAGGCGC | 55666 |
rs753758674 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589401 | GGGTGCGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 55666 |
rs753779070 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598587 | GCCGGAAGGAAGCAT[C/G]TGAGGGTATGAGGAT | 55666 |
rs753833374 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581984 | GACAGCAGAGACATG[C/T]TTCCATGGTGGACCC | 55666 |
rs753845357 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587715 | GTCTAGCTCTGTTCC[C/T]CAGGCTGGAGTGCAG | 55666 |
rs753866949 | snp | A/G | 3.25887e-05 | 0.00403649 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567570 | TGAATGTTCCATACA[A/G]TTCCCCAGTGCCAGA | 55666 |
rs753872876 | snp | C/T | 1.65866e-05 | 0.00287976 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81569038 | TCACCCAATACATCC[C/T]GGTTTTCAATAGGAA | 55666 |
rs753948859 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558132 | GGAACGCAGAGCACA[C/T]AAGCAGGACCCCACC | 55666 |
rs753957068 | snp | A/G | 3.37092e-05 | 0.0041053 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604594 | GCCCTGATGCCAAGG[A/G]GAATGTCTTTGTGCT | 55666 |
rs753957548 | snp | A/G | 2.99415e-05 | 0.00386909 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600467 | TGGACTTAGAGCAGA[A/G]GGCTCAGGAAGCAGC | 55666 |
rs753984706 | snp | C/T | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556576 | ACATGTACCTGTCCA[C/T]AAAGCAGTGACTGTG | 55666 |
rs753986794 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566076 | CAGTGGCTCACGCCT[A/G]TAATCCCAACACTTT | 55666 |
rs753991257 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575832 | AAAATTTTCTCTTAA[C/G]ACTGGGAATATGCTA | 55666 |
rs753993651 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637278 | TCCTCGGAAACCCAA[C/G]CGGCACAGGAAAGTC | 55666 |
rs754045587 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590423 | CTGAGCCTTTGGAGG[A/C]GGCAGGCATGGGGGA | 55666 |
rs754053952 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589271 | TGCGGTGGCTCATGC[C/T]TGTAATCCCAGCACT | 55666 |
rs754081481 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595294 | CAAAAATTAGCCAGG[C/T]GTGGTGGTGTGCACT | 55666 |
rs754081963 | snp | C/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636132 | GCGCCATGACGCCCG[C/G]CTAATTTTTTGTATT | 55666 |
rs754131271 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603630 | ATTAAAAATTTCTAA[C/T]ATACAGCTAATTTAA | 55666 |
rs754192197 | in-del | -/AA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611961 | GAGAGTCCATCTCAA[-/AA]AAAAAAAAAAAAAAA | 55666 |
rs754200029 | snp | A/G | 6.64319e-05 | 0.00576295 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622118 | TCGGGCAGATCATGG[A/G]GACCTCATTTCCCCC | 55666 |
rs754243833 | snp | G/T | 2.99039e-05 | 0.00386666 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81559301 | GCAGTGGCCTGTGCC[G/T]GGCTGGTTCATGAAC | 55666 |
rs754245301 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595531 | TATACATATATATAT[-/T]ATATTTTTTTTTTCT | 55666 |
rs754248474 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619118 | ACCTTTGTTCACTTG[-/T]TTTGGCTGCTGACCT | 55666 |
rs754262657 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584450 | TTTCCAATCTGAAAA[C/G]GGTATTTAAAAATAA | 55666 |
rs754372358 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635113 | TTGGTATGCCAAGGC[A/G]GGCGGATCACGAGGT | 55666 |
rs754407567 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595922 | GTTATGAGTTTTGGG[A/G]TTTGTGTTTATATAG | 55666 |
rs754419601 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583597 | TCCTGGTCCTCACAG[A/G]ACTATGTGTACACCC | 55666 |
rs754426904 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628726 | AAGATAAGCTAAGAA[C/G]TACATAATATGCAAC | 55666 |
rs754446902 | snp | C/T | 1.75053e-05 | 0.00295844 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588926 | TGTACAGAGTTCTTT[C/T]TCTTACCATACTTTT | 55666 |
rs754490211 | snp | A/T | 6.7184e-05 | 0.00579547 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606656 | TCCGTTTCTCAGCCA[A/T]GAAAACAAATCTAGA | 55666 |
rs754499841 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607972 | GCTGAAGCCTGCTAC[C/T]TTCTGGTAGGGTGTA | 55666 |
rs754560605 | snp | A/G | 0.000146488 | 0.00855702 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565427 | TCCAGGGCACCACCG[A/G]CAGTGGGGAGCTGTG | 55666 |
rs754575970 | snp | A/C/G | 1.65674e-05 | 0.00287809 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629825 | TGCAAACAAAACATG[A/C/G]TGGTTACTGCACAGC | 55666 |
rs754629900 | snp | C/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81566594 | CTGATGTCAAATACC[C/T]GAGTGAGTGGTTTTG | 55666 |
rs754638394 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583795 | CTGAAGGACAGTCAG[A/G]AAGCTTCTACTCCCA | 55666 |
rs754644010 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629332 | AAGTAGCTGGGATTA[C/T]AGGCACCTACCACCA | 55666 |
rs754667635 | snp | C/T | 1.65792e-05 | 0.00287912 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629697 | GGATGAAAAATATCC[C/T]GAGGGTCAATACCCA | 55666 |
rs754689814 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585083 | GCTGAGGCAGAAGAA[C/T]TGCTTGAACCCGGGA | 55666 |
rs754692366 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558918 | GCTGGGTGGTGGCAG[C/T]ATCGGCCCCTCCCTG | 55666 |
rs754694195 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570009 | ACTATTCTGGTTCCT[C/T]TGGGACTATTTCTAA | 55666 |
rs754736192 | snp | C/T | 1.65773e-05 | 0.00287895 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597211 | TCTGTAACCAAGCCA[C/T]AGGGCCACACGCACA | 55666 |
rs754759844 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634486 | AACACTTTTCACTTG[C/T]CAATGGTTATTTTAA | 55666 |
rs754764072 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621305 | AAGAACAAATGAATG[C/T]TACAATTGCATGTTG | 55666 |
rs754788109 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586739 | CCTTTCAGGGCCAAT[A/G]AGACAAAGATTTAAG | 55666 |
rs754804260 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580104 | GTGCTCTCCACCTCA[A/T]TCCCCCAAGGTGGGG | 55666 |
rs754823983 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600586 | CACATGCGACACGCC[C/T]CCCGGCTTCTCTCCT | 55666 |
rs754847799 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633631 | AACTTAAGTTTCCCT[A/G]TTTATAAGAAAATAA | 55666 |
rs754868807 | snp | A/G | 7.03755e-05 | 0.00593151 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610268 | CGGCATCTGAGGAGA[A/G]TACAAGGCAGAAAAA | 55666 |
rs754888368 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569203 | CTCCCAGAGCCCAAA[C/T]TAACGACTCCTAGCA | 55666 |
rs754892717 | in-del | -/GTACTCAC | 0.000189952 | 0.0097437 | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563909 | GGGAGCTAAACATGG[-/GTACTCAC]GTACATAAAGATGGC | 55666 |
rs754894141 | snp | A/C | | | missense, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81589009 | AGCCAAGCTCCGGGG[A/C]GTCCTTGCATGGCAG | 55666 |
rs754951523 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563485 | TGATGCAGGAGGATC[A/G]CTTGAGCTCAGGAAT | 55666 |
rs754965194 | in-del | -/GGATGGTCTCAATCTCCTGACCTTGTG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629090 | TCACCATGTTAGCCA[-/GGATGGTCTCAATCTCCTGACCTTGTG]ATCCGCCCGCCTCGG | 55666 |
rs754982632 | in-del | -/TTTC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595037 | GTCAGCTTGAACACT[-/TTTC]TTTCTTTTTTTCCAA | 55666 |
rs755005333 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612838 | TGCAGGGATGGAGAG[C/T]GCACACTAGTGTGGC | 55666 |
rs755020601 | in-del | -/CAC | 1.68393e-05 | 0.00290161 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613279 | TTCACCCATTAAGAT[-/CAC]CACAAGTAGGACCCT | 55666 |
rs755153960 | snp | A/C/G/T | 3.47337e-05 | 0.00416721 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567577 | TCCATACAGTTCCCC[A/C/G/T]GTGCCAGACCCCGAA | 55666 |
rs755154984 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612584 | CAATACCTCAAAGTC[A/G]GCACCCCGTCACATC | 55666 |
rs755199456 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599897 | CTCCAAGTGCATGGC[A/G]CAGAACATGAACACT | 55666 |
rs755213356 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602234 | CAAAACAAAACAAAA[-/C]AAACAAACAAACAAA | 55666 |
rs755241673 | snp | C/T | 4.02787e-05 | 0.00448751 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604504 | GGCGTCCCCCACAGC[C/T]TCCAAACACAGAAAC | 55666 |
rs755299507 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557774 | CACAATAGCTCTGCC[A/G]TGACCAGACCCAACC | 55666 |
rs755299655 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567299 | ACAACCTGTGACCCC[A/G]AGCTTTGACCCAGTT | 55666 |
rs755373731 | snp | C/T | 2.93699e-05 | 0.00383198 | missense, nc-transcript-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81559305 | TGGCCTGTGCCTGGC[C/T]GGTTCATGAACGTGC | 55666 |
rs755381263 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620225 | ATAAAGAGCCAGGCA[C/T]GGTGGCTCACACCTG | 55666 |
rs755417329 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603934 | ATAAATATACACACA[C/G]AGCCCAATTCCCAAA | 55666 |
rs755419293 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578750 | ATTCAATTATCTCCA[C/T]CTCATCTCTCCTTGA | 55666 |
rs755424533 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624668 | AAATGGGGGAGACAA[A/G]GTCAACAAAGGTCGA | 55666 |
rs755514980 | in-del | -/AAGGCC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619068 | ACACAAACACTGCGG[-/AAGGCC]AAGGCCGCAGGGTCC | 55666 |
rs755532885 | snp | C/G/T | 0.000418967 | 0.014468 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559231 | GGGCTGGGCTGGGCC[C/G/T]GGTCCTAGCCAGCAG | 55666 |
rs755555599 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619553 | GAAACTCTGTCTCAA[-/G]AAAAAAAAAAAAAAA | 55666 |
rs755565319 | snp | G/T | 3.36038e-05 | 0.00409888 | synonymous-codon, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81589085 | GTACCCTTCAAAGTG[G/T]ACTTGGTTGTCAGGA | 55666 |
rs755643109 | snp | C/G | 2.27876e-05 | 0.00337539 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559393 | CGTACTCATGGAGAC[C/G]TGGGAGCTGCCCGCC | 55666 |
rs755654201 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598514 | GAAAGGCACATAATA[C/T]AAAAGGGGTAATATA | 55666 |
rs755743328 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576083 | TGGCACAGAGGACGA[C/T]GACCAGAAGTAAGAC | 55666 |
rs755765786 | in-del | -/ACCCA | 1.66385e-05 | 0.00288426 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567578 | CATACAGTTCCCCAG[-/ACCCA]TGCCAGACCCCGAAA | 55666 |
rs755810288 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585351 | AAAACTGTGCTCATA[C/T]AGCTGATTATCCACA | 55666 |
rs755827243 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568573 | TGGCCTGATCTGCCA[C/G]TGAGAGCAGAGGCCA | 55666 |
rs755857507 | snp | C/T | 3.55189e-05 | 0.00421405 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608859 | GAGTGCAGTCTCACA[C/T]GTGCCGGTCACTCCA | 55666 |
rs755877984 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580192 | ACCACCCCAACACCA[C/T]CTGTACCATGTGCCT | 55666 |
rs755895053 | snp | A/G | 1.93082e-05 | 0.00310704 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589138 | TAAAAAGAGTCTACC[A/G]AACGGCATTCAAAAC | 55666 |
rs755909181 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570416 | ACAAAAGCCTGGCCT[A/G]CTCAGGCGCGTCCCT | 55666 |
rs755922137 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608119 | GCCTGTGGGCAACTA[C/T]TGTGGTACCATGAGG | 55666 |
rs755924065 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571464 | GCTCCTGGAGTTCCA[C/G]CCAGTAAACCACGCT | 55666 |
rs755947316 | snp | A/G | 1.6741e-05 | 0.00289314 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608708 | ATTTACGCACAACCA[A/G]GTTACAGCAAGTTGC | 55666 |
rs755962430 | in-del | -/C | 1.66117e-05 | 0.00288194 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622120 | GGCAGATCATGGGGA[-/C]CCTCATTTCCCCCCA | 55666 |
rs755965813 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589220 | TCAAGAGTTTGTCGG[G/T]GGTAAGAGTTAAAAA | 55666 |
rs755982435 | snp | A/T | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636062 | ACTGTAACCTCCACC[A/T]CCCGCGTTCAAGCAA | 55666 |
rs755986626 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566712 | TCTCTATTCTGTCTC[C/G]TTCAGGGAAAAGTTC | 55666 |
rs755997193 | snp | C/T | 2.58957e-05 | 0.00359822 | synonymous-codon, nc-transcript-variant, missense | NPLOC4 | GRCh38.p7 | 17:81559352 | CATGGCTGCAGTGGC[C/T]GTGTGTGTGGAGCCC | 55666 |
rs756081665 | snp | A/G | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556516 | CCTTGCTGCACCTGT[A/G]CAGTCTGGCCTTCCT | 55666 |
rs756104495 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615520 | AAAATCAATTGATGA[A/G]CTCTAAAGAAAGTAG | 55666 |
rs756227894 | snp | C/T | 2.26416e-05 | 0.00336456 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567406 | AGTGGACACCACACT[C/T]GGACACGCACCTGCA | 55666 |
rs756263328 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613976 | ATAGGAGCTGTCACT[A/G]CTTTTAAAAAGTGTG | 55666 |
rs756273305 | snp | C/G | 2.32788e-05 | 0.00341158 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81600346 | GCCTCAGTACCTTCC[C/G]CAGGCCAAGTTTGGC | 55666 |
rs756286129 | in-del | -/AC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593101 | CTCTGAATGCCCGCT[-/AC]ACACTTGTGTAGGCA | 55666 |
rs756315514 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592274 | GGGTCCCCGCATGGC[C/T]GTGACCAAGAAACCC | 55666 |
rs756341848 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588528 | ACCACATCTACTTTT[A/T]GTAGAGACACAGTCT | 55666 |
rs756378686 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636663 | ATTCTCCCTGCTTAG[-/AA]AGGCTCGGCCTTTCC | 55666 |
rs756396599 | snp | A/G | 3.3129e-05 | 0.00406982 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613387 | TCAATCTCATCCTCC[A/G]CCACGTTGGGAGCGC | 55666 |
rs756398849 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593889 | GCCCTAACAGGTTCT[A/G]TAATGCAGAATTCCC | 55666 |
rs756405131 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590343 | TCATGGCTGAGAGGC[A/G]GCAGTGTGGTCCAGT | 55666 |
rs756405430 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615050 | CTCTTCCTCCCTAAT[C/T]TGGGGGTGATGAACA | 55666 |
rs756410877 | snp | A/G | 5.60271e-05 | 0.00529249 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559217 | TCTGGCTTCAGGAAG[A/G]GCTGGGCTGGGCCCG | 55666 |
rs756421909 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562314 | GAAGCCGAGGTGGGT[A/G]GATCACTTGAGGTCA | 55666 |
rs756502733 | snp | C/T | 5.30762e-05 | 0.00515124 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588911 | TCACACCATTCTCCA[C/T]GTACAGAGTTCTTTT | 55666 |
rs756551777 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633862 | AGGCGCCCGCCACCG[C/T]GCCCAGCTAATTTTT | 55666 |
rs756597028 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583025 | GCCCATGTGCGCCAG[C/T]ACAGCAGCCACTGCC | 55666 |
rs756658016 | snp | C/T | 5.84266e-05 | 0.00540462 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81572083 | GTTGCCAAACTTGTC[C/T]ACGTCCTGCAATAGT | 55666 |
rs756669756 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583115 | AACTCTTCTTCCTAA[C/T]TATCAAGAGAGATGT | 55666 |
rs756694072 | snp | C/T | 3.33333e-05 | 0.00408235 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606748 | GATGCCATTCGGCCA[C/T]GGGAGGTGCCCCTCG | 55666 |
rs756705694 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620313 | CCAGCTTGGCCAACT[C/T]AGTGAAACCCCACCT | 55666 |
rs756798454 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586427 | CCGGCCTGGCCAACA[C/T]GGTAAAACACAGTCT | 55666 |
rs756808590 | snp | A/G | 8.0443e-05 | 0.00634153 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559338 | TGCTGACAGGCCCAC[A/G]TGGCTGCAGTGGCCG | 55666 |
rs756854746 | snp | A/G | 2.47939e-05 | 0.00352084 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567556 | AATGGGAATAAACAT[A/G]AATGTTCCATACAGT | 55666 |
rs756856127 | in-del | -/TCA | 0.00214305 | 0.0326639 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637447 | GGCAGGATCACACCT[-/TCA]TGTTTTTTTTTTTAA | 55666 |
rs756887145 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602393 | GTATAAAAAAAAAAA[G/T]TAAACAATTAAACAA | 55666 |
rs756887976 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599467 | CTAAATCAAGATGCT[A/G]ACTCCTTGTTAGAAA | 55666 |
rs756891979 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585565 | TACTCGGGAGGCTGA[C/G]GCAGGAGAATCGCAG | 55666 |
rs756907383 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604999 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 55666 |
rs756933856 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600016 | GCCAGCAGGGGTGCG[A/G]CTGGGGTCTGTTTCC | 55666 |
rs757013726 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572417 | AGGATGGTCTCGATC[G/T]CCTGACCTCGTGATC | 55666 |
rs757026400 | snp | A/C | 3.45728e-05 | 0.00415755 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606803 | ATGTTCTCCAGGGCA[A/C]CAAACTTCCCCCTAC | 55666 |
rs757036705 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81611773 | GACCATCCTGGCAAA[C/T]ACGGTGAAACCCCGT | 55666 |
rs757049936 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609371 | CCAGGTTGGAGTATG[A/G]TGGTGCAATCATGGC | 55666 |
rs757066845 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624056 | TCGGGAGGCCAAGGC[A/G]GGTGGATCACTTCAA | 55666 |
rs757081155 | snp | A/T | 0.000185925 | 0.00963993 | missense, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637399 | TCCAAACTTCTCTCC[A/T]TGCACAGGTAAGTAG | 55666 |
rs757139572 | snp | A/G | 2.64554e-05 | 0.00363689 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567376 | GTCTCTTTGCAGCCA[A/G]AGCCCACTTGCTCAA | 55666 |
rs757166862 | snp | A/G | 0.000255722 | 0.0113047 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565481 | CAGCCACGGGGTGCC[A/G]GGGCAGGGGGTGGGG | 55666 |
rs757205900 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571552 | GGAGTGACCCAGACA[C/T]ACTGTGGGCTGTGGC | 55666 |
rs757269901 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589467 | GGCGTGAACCCGGGA[A/G]GTGGAGCTTGCAGTG | 55666 |
rs757323442 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589337 | AGATCGAGACCATCC[C/T]GGATAACACGGTGAA | 55666 |
rs757331631 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558936 | CGGCCCCTCCCTGTG[C/T]GCCCCAATTCCAGGT | 55666 |
rs757343309 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558149 | AGCAGGACCCCACCA[C/T]GTGCTGTTCCAGATC | 55666 |
rs757373692 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603692 | CACTAGATTCACCAT[A/G]AACATTTCCTATGCA | 55666 |
rs757385847 | snp | A/C | 1.66015e-05 | 0.00288105 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597353 | TTTAAACATCTCCTC[A/C]AGATAGACGATGAAT | 55666 |
rs757459587 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557524 | TCTAGAAGTCCGTGC[C/T]GTCCAGCCTCTGCCC | 55666 |
rs757468889 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637315 | GGAAGCAAAGACGAG[C/T]ATCCGAAGTCTCACC | 55666 |
rs757487793 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580397 | CTCCTTTTCCAGCTC[C/T]GAGCCCAGCAGCCAG | 55666 |
rs757513799 | snp | C/T | | | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565221 | GATGTTCAAAGTGCT[C/T]CTAGGATGCCTGGAG | 55666 |
rs757523494 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627904 | TCACGCCACCACATT[C/T]CAGCCTGGGCGACAG | 55666 |
rs757542656 | in-del | -/AAAAAAAAAAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628213 | GAGACTCCCTCTCAT[-/AAAAAAAAAAA]GAAAAAAAAAAGAAA | 55666 |
rs757590177 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583601 | GGTCCTCACAGGACT[A/C]TGTGTACACCCATAT | 55666 |
rs757617712 | snp | C/T | 1.68179e-05 | 0.00289977 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606646 | TCTGGAAATATCCGT[C/T]TCTCAGCCATGAAAA | 55666 |
rs757646166 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614081 | AAAGATCAAGACCAT[C/G/T]CTGGCCAACAGGGTG | 55666 |
rs757673898 | snp | C/T | 1.6842e-05 | 0.00290184 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569126 | TCTAATGAAGAAAAA[C/T]ACAAACCCATGATAA | 55666 |
rs757699660 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615612 | CAGAGCTGCTTGTGG[C/G]GCCAAGGCCACTCTC | 55666 |
rs757706072 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575875 | CAGAATCTCTTCTGT[C/T]GATGGCAGTTTCTTG | 55666 |
rs757737774 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627697 | TGCTTGAACACAGGA[G/T]GCAGAGGCTGCAATG | 55666 |
rs757782108 | snp | A/C | 1.68672e-05 | 0.00290402 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604632 | CCGTCCGTATAAGTA[A/C]CCAAAATGCTGGTTC | 55666 |
rs757803750 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566374 | CGGATAAAGCCTTCA[G/T]GAGCTCTCAGTACCT | 55666 |
rs757835932 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615755 | CAGATAACCAAAGGA[C/T]GCCTGAACAGCTGTG | 55666 |
rs757877949 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621923 | GACAAAGACAATAAC[C/T]TTCTCCTCAGTGACA | 55666 |
rs757887599 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621241 | AAGAGGTTTCGTTTC[A/G]CCTCACCACATGGGT | 55666 |
rs757911889 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619300 | GAGAATGGCATGAAC[A/C]CGGGAGGTGGAGCTT | 55666 |
rs757912435 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588045 | GGAAGCAATTAACAA[C/T]TTAAACTTCTGGAAT | 55666 |
rs757950610 | snp | A/C | 3.47832e-05 | 0.00417018 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588932 | GAGTTCTTTTTCTTA[A/C]CATACTTTTACCTTA | 55666 |
rs757958592 | snp | A/G | 2.19156e-05 | 0.00331019 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606861 | ATTGGTGAAAAGTTG[A/G]GCAAGAGGCTGGAAA | 55666 |
rs757960853 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579339 | GCCAAGATCGTGCCA[C/T]TGCACATCACCCTAG | 55666 |
rs757998132 | snp | C/G | 7.82411e-05 | 0.00625415 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636971 | GAGCCCCGGGCCGCC[C/G]CCGCCTGCCGCCCCA | 55666 |
rs758001843 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636360 | TGTCCTTCCAAGTAA[A/G]GAGCAAAGCCGGCAA | 55666 |
rs758048463 | snp | C/T | 1.68185e-05 | 0.00289982 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606762 | ACGGGAGGTGCCCCT[C/T]GCACCCTGACTTAAT | 55666 |
rs758050758 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578264 | TGCTCTCCAGGTACA[C/T]AGCTTCAGCAGATTC | 55666 |
rs758054216 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594397 | CACCCTCAAAAAGTA[C/T]ATTCATTTCAAAAAT | 55666 |
rs758074329 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607925 | TTCAGCCACCATCTC[C/T]TCGTTGCACTGACAG | 55666 |
rs758138316 | snp | C/G | 1.67256e-05 | 0.0028918 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606674 | AAACAAATCTAGACA[C/G]ACAGGGAACATCTCA | 55666 |
rs758144765 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567668 | CTGCCTCTGCAACCA[C/T]GAACAGGGTCCAAGA | 55666 |
rs758151342 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627156 | GGCACATTGGGAGGC[C/T]GAGGCAGGCGGATCA | 55666 |
rs758174114 | snp | C/T | 1.65693e-05 | 0.00287826 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629833 | AAACATGATGGTTAC[C/T]GCACAGCCTAGTGAG | 55666 |
rs758177771 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598741 | GCAGCAGTTGAGTCC[C/T]GGCAATTGTCACTTC | 55666 |
rs758194609 | snp | A/G | 0.000278435 | 0.0117958 | intron-variant, synonymous-codon | NPLOC4 | GRCh38.p7 | 17:81565461 | AGTGGGCTGCTCTCC[A/G]GCCCCAGCCACGGGG | 55666 |
rs758240188 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612712 | GTTTATTTAAAAGGA[A/C]TTGCAAAAAATCTAA | 55666 |
rs758256752 | snp | C/T | 0.000404886 | 0.0142225 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563949 | CGCCAGGTGTGGTGG[C/T]ACACATCTGTAATCC | 55666 |
rs758282787 | snp | A/C/G | 3.315e-05 | 0.00407113 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597328 | CAACCTTAAAAAAAG[A/C/G]AAAGTAGCTTTTAAA | 55666 |
rs758284073 | snp | C/T | 1.65748e-05 | 0.00287874 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597219 | CAAGCCATAGGGCCA[C/T]ACGCACAGTCCTGTC | 55666 |
rs758317965 | in-del | -/TTTTA | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637459 | CCTTCATGTTTTTTT[-/TTTTA]AGTATTTTTTAAATT | 55666 |
rs758344457 | snp | C/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560996 | CCTTTTTTTTGTTGT[C/T]GCCGAGGCTGGAGTG | 55666 |
rs758352046 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620396 | AGCTACTCAGGAGGC[C/T]GAGGCAGGAGAAATG | 55666 |
rs758359759 | snp | A/G | 3.52355e-05 | 0.0041972 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610301 | CAGAGCAGTGAGGAT[A/G]TCTGTGTTCCGCTGC | 55666 |
rs758370557 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586514 | ACTCGGGAGGCTGAG[C/G]CACAAGAATCGCTTG | 55666 |
rs758396510 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633230 | ACGTTTTCACAATAT[A/G]TAGCATTAGGTAAAT | 55666 |
rs758412975 | snp | C/T | 1.65641e-05 | 0.00287781 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613360 | TTCCCGTCCTGTTTG[C/T]TGAGGTACTGATCAA | 55666 |
rs758474627 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572483 | GGCGTGAGCCACCGC[A/G]TCCGGCCTTCACTTT | 55666 |
rs758481390 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571599 | GGGCAAGCACCTGCA[C/T]GTGCAGGACAGCTGA | 55666 |
rs758508912 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587825 | AGGTGCCTGCTACCA[C/T]GCCCGGCTTATTTTT | 55666 |
rs758534654 | snp | G/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637518 | TAAACTGCATTTCAG[G/T]CCGGGCGCGGTGGCT | 55666 |
rs758536511 | in-del | -/GCAGAGG | 1.66327e-05 | 0.00288376 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559243 | GCCCGGTCCTAGCCA[-/GCAGAGG]GCAGGCGCCCTAGGT | 55666 |
rs758551563 | snp | A/G | 2.10281e-05 | 0.00324247 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81572026 | ACTTACGTCTATGAT[A/G]AGATACTCCACAGGC | 55666 |
rs758571017 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582119 | TAGACAGAGCCAGTC[A/G]GAAGACTTACTTGGG | 55666 |
rs758594797 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616732 | AAGACTCCATCTCAA[-/A]AAAAAAAAAAAGAGT | 55666 |
rs758610446 | snp | A/C/G | 7.08065e-05 | 0.00594964 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604683 | AAGAAAGCGGTCAGC[A/C/G]ACGGTGTGATTCTCA | 55666 |
rs758621920 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558964 | GGTGCCACGTAGAGG[C/T]GAGAGGTCTTTCCAA | 55666 |
rs758643845 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616828 | CTCAGACACAGAAAT[C/T]ATGAGACCGAATATC | 55666 |
rs758660379 | snp | A/G | | | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565408 | GATGCAGCTGGGTGC[A/G]GAATCCAGGGCACCA | 55666 |
rs758677465 | in-del | -/AAGG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621053 | AGGAAAAGGAAAAGA[-/AAGG]AAGGAAGGAAGGAAG | 55666 |
rs758725881 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630432 | GCTGGAACCACAGGC[C/T]TGCACCACCACACCA | 55666 |
rs758734396 | snp | C/T | 1.68134e-05 | 0.00289938 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604618 | TTGTGCTCCGTGTAC[C/T]GTCCGTATAAGTACC | 55666 |
rs758737375 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576668 | TGTGTTTGCAACACA[C/T]GACAAAGGGTTAATA | 55666 |
rs758742235 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575632 | GCTGGACAGCTGTGT[A/G]GAGACTGGGCCCCCC | 55666 |
rs758750184 | snp | C/T | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556696 | CCCCAGATGTTAGCA[C/T]TTTAAGAAACTTATC | 55666 |
rs758754140 | snp | A/G | 5.04774e-05 | 0.00502356 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622324 | ATGAAATGCTAAAGT[A/G]TCACTACACATACCA | 55666 |
rs758765380 | in-del | -/CCT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627199 | TCGAGACCATCCTCA[-/CCT]CTAACACAGTGAAAC | 55666 |
rs758822414 | snp | C/T | 1.89213e-05 | 0.00307576 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604534 | CTCAGGAACTTGAAT[C/T]CCGTCATGTTTACCT | 55666 |
rs758829452 | snp | A/C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584638 | ATGGAAAGGATAATA[A/C/T]GTGTAGGAAATGCGA | 55666 |
rs758849943 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597556 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACCCGAG | 55666 |
rs758908130 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565681 | CTAGAACAGGTTTCT[C/T]TCTCCCCAACATCAA | 55666 |
rs758938337 | in-del | -/CTCA | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578949 | ATTTAGAGACAGGGT[-/CTCA]CTATGTTGCCCAGGC | 55666 |
rs758955791 | snp | A/G | 1.65638e-05 | 0.00287778 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622232 | GTCTTGTTTCTATTG[A/G]TGTAAACCGAGAAGC | 55666 |
rs759007754 | snp | A/G | 6.75668e-05 | 0.00581196 | synonymous-codon, nc-transcript-variant, missense | NPLOC4 | GRCh38.p7 | 17:81559385 | GACGGCGCCGTACTC[A/G]TGGAGACCTGGGAGC | 55666 |
rs759019674 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572153 | TGATTTTCCTTTCAC[A/G]TGCTTGTCTCACCTT | 55666 |
rs759049577 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571257 | GCGTGGCAGCAGCAT[A/T]GGAAATGAGCCGCCT | 55666 |
rs759070189 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580810 | ATGAGAGAATGGATG[C/T]CGTGAGAGCATCGCA | 55666 |
rs759070898 | snp | C/G | 5.75473e-05 | 0.0053638 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636951 | CTGCTCCTGCCTCCG[C/G]GCTCGAGCCCCGGGC | 55666 |
rs759081337 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624303 | GACACTTGTTATCCC[A/C]GCTACTCAGGAGGCT | 55666 |
rs759084974 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588799 | TCCAGCCCCAGAAAC[-/G]TGACAGAAGCCTTTA | 55666 |
rs759122925 | snp | C/T | 7.08416e-05 | 0.00595112 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600311 | AGAGCCTGGCCACGC[C/T]CCCTGCTTGGCTGCC | 55666 |
rs759162916 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622952 | GTAATCCCAGCACTT[C/T]GGGAGGATGAGGTGG | 55666 |
rs759205939 | snp | G/T | | | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564905 | CCCGGGCACTCTGGT[G/T]CTCTCAGCTGCAGGG | 55666 |
rs759208721 | snp | A/G | 4.9689e-05 | 0.00498418 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81597293 | GGTATCTTCTGAGAC[A/G]AGGTCTGTAAATATC | 55666 |
rs759219835 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557226 | TGGCTGAGCCTCCCA[A/G]GGCCTGAACTCTCAC | 55666 |
rs759262681 | snp | C/G | 1.66349e-05 | 0.00288395 | missense, upstream-variant-2KB, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613427 | TGAAGCCCGGTGGAA[C/G]TGACGTCTCCATTTC | 55666 |
rs759291809 | snp | C/T | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556435 | TTGTTCTAGACGCTT[C/T]CTGTTGTCACAGGGA | 55666 |
rs759292309 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601816 | TCCGTATAAATACAG[C/T]CAAGAAAGACACACA | 55666 |
rs759310317 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629962 | TCAATCCTTCTAGAA[C/T]ATGATGCCGAGGGGT | 55666 |
rs759334260 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81608822 | AGTCCTCATCGAATG[C/G]CTGCCAAGACACAGA | 55666 |
rs759362208 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632497 | TTTAGTATTTTTAGT[A/G]GAGATGGGATTTCAC | 55666 |
rs759470457 | in-del | -/AC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598805 | CTCCAGCACTACCTG[-/AC]ACACAACTCTTCCCA | 55666 |
rs759514610 | snp | A/G | | | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565068 | TGCGGTCCGTTCCGT[A/G]GTGTCCACCAGCAAC | 55666 |
rs759640951 | snp | A/G | 4.35559e-05 | 0.00466648 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604745 | GTAGAGTTAACAAGA[A/G]TGGGCTGATGAAAAC | 55666 |
rs759668591 | snp | C/T | 1.65614e-05 | 0.00287757 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81629779 | TGTGATCCGCTTCAC[C/T]CCATCCGGGGACTGG | 55666 |
rs759695076 | in-del | -/TCTT | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567215 | AGGTGAAAAAATTAA[-/TCTT]TCTTTCTATCAACAA | 55666 |
rs759712196 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614736 | AAACTGCTGACCTCA[A/G]AGGCTAACAAGCATC | 55666 |
rs759754199 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634920 | AAGGTTTCTTGGCCG[C/G]GCATGGTAGCTCAGG | 55666 |
rs759756361 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558693 | GAGAGGAGGAGGGCA[A/G]GCAGCAAACCGACCT | 55666 |
rs759865873 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583499 | CCCTTTCACAAGAAA[A/G]GTGAAAGAGAAAAGC | 55666 |
rs759906927 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579928 | TGTGAGCTCACTCTC[A/G]GCAGCCGCTTATCTA | 55666 |
rs759946501 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568503 | TATGATTTAAGAACA[A/G]CCATGTGTACACAGC | 55666 |
rs760019142 | in-del | -/TTGT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601382 | GCTAAGGAAAAGGAG[-/TTGT]TTAATGACATGTGGC | 55666 |
rs760028492 | snp | C/T | 1.70006e-05 | 0.00291548 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610178 | CGCAGCCCCCCACAC[C/T]GGCCCAGAACTTACT | 55666 |
rs760060515 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573234 | TTCCAATTATAGGGC[C/T]TTACATAAAAGTTTA | 55666 |
rs760098256 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605997 | AGCTAATTTTTTGTA[C/T]TTTTAGTAGAGATGG | 55666 |
rs760124932 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579045 | CCTGCCTCAGCCTAC[C/T]GAGTACCTGGGGCCA | 55666 |
rs760148210 | snp | C/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561998 | CAGCACTTTGGGAGA[C/G]CGAGGCAGGTGGATC | 55666 |
rs760150540 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625006 | TTGCTCAACACCACA[A/C]TGAAGAGGAAGCTAG | 55666 |
rs760167324 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582622 | CACACAGACTGGCCT[C/T]GACTTCCTGAGCTCA | 55666 |
rs760174703 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572907 | AAATGAGCGCACACA[C/T]AAATATGAAGACACG | 55666 |
rs760176796 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586276 | CAGGAATTTCAAACA[C/T]GCAGCCATTCTCTCC | 55666 |
rs760190145 | snp | A/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560822 | ACGGTTTTGCCTCCC[A/T]CTCGCAAGGTACGAG | 55666 |
rs760229550 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612358 | CAGAATTCTCTCACA[C/T]ACACACGCTCTCAAA | 55666 |
rs760238609 | snp | A/G | 6.64651e-05 | 0.00576438 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613324 | ATCACTTACAGCTGT[A/G]GGTCTCGGCTTCTGT | 55666 |
rs760243065 | snp | A/C | 1.66815e-05 | 0.00288799 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596292 | GCATCATGCCAAAAT[A/C]TACTTCTATTTCTTC | 55666 |
rs760246232 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591583 | TTTATAAAACTGAAG[A/G]CTGTTTATAAACAGC | 55666 |
rs760289857 | in-del | -/AA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572985 | AGATGCACAGAACAT[-/AA]AGTTTAATTATGGGG | 55666 |
rs760335706 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600252 | AGCCAGTACCCGACA[C/G]AGCCCGGCCACTCTC | 55666 |
rs760358634 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604429 | TGTTGTGCACGTGCA[C/G]CGGTGTGTGACAAAG | 55666 |
rs760398769 | in-del | -/AAAAAAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623465 | GCAAGACTTTGTTTC[-/AAAAAAA]AAAAAAAAAAAAAGC | 55666 |
rs760438932 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590397 | TGGGCAGATGATGCC[A/G]TGGGGGCAGCCTGAG | 55666 |
rs760444952 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617183 | CAATGTGGCAGCAGA[G/T]CAGAAACTAGGAGAA | 55666 |
rs760463136 | snp | C/T | 5.6214e-05 | 0.00530131 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604708 | TTCTCAAACATGATA[C/T]TGTCCACATGCCTGT | 55666 |
rs760495380 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81566627 | ACAAAATACAGACAC[A/G]AAATAAACTAGCAGG | 55666 |
rs760520883 | in-del | -/TCT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575826 | AGATGCAAAATTTTC[-/TCT]TAAGACTGGGAATAT | 55666 |
rs760558037 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557948 | AATGTGGGTCACGTG[C/G]GCTTACCCCCCAGGA | 55666 |
rs760582821 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603499 | TACTCAGAAGGCTGA[C/G]GCAGGAGGATCGCTT | 55666 |
rs760587438 | in-del | -/GGT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612296 | GTGCTGCGGAACAGA[-/GGT]GGCCTCTGTGCTTCC | 55666 |
rs760653260 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584233 | GATATTTTCCTGAAA[C/T]ATGAGAAATCTGTCT | 55666 |
rs760690441 | in-del | -/TTTTTTTTTTTTTTTTC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631446 | ATATATTTTTTTTTT[-/TTTTTTTTTTTTTTTTC]TTTTTTTTTTTTTTT | 55666 |
rs760690967 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565988 | TCTTTCTCCTCTCGT[A/G]TCTGGAAAAATGCAC | 55666 |
rs760735749 | snp | C/G | 3.31246e-05 | 0.00406955 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622177 | TTACTTGATTTTTAG[C/G]AAGTTGAGGGATTTG | 55666 |
rs760752376 | snp | C/T | 7.15299e-05 | 0.00597995 | missense, nc-transcript-variant, synonymous-codon | NPLOC4 | GRCh38.p7 | 17:81559375 | TGGAGCCCCCGACGG[C/T]GCCGTACTCATGGAG | 55666 |
rs760787850 | snp | A/G | 0.00994489 | 0.0698108 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622243 | ATTGATGTAAACCGA[A/G]AAGCCATTATTTTGG | 55666 |
rs760838380 | snp | C/T | 1.65875e-05 | 0.00287984 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596116 | CTGTCCCTGTTATAC[C/T]TGTAGCCACTGCAGT | 55666 |
rs760843013 | in-del | CCCC/TTTTTTTTTT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631453 | TTTTTTTTTTTTTTT[CCCC/TTTTTTTTTT]CCCCCACGGCAAGCC | 55666 |
rs760872200 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616787 | TGGGCAGAGACATAA[C/T]TAACAGAGAGTTAGA | 55666 |
rs760891639 | snp | A/G | | | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565048 | TCCGGAAGACACGCA[A/G]TGCCTGCGGTCCGTT | 55666 |
rs760924601 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576474 | TGGGGCGTGAGTGCA[C/T]GTGGACTTGACTATA | 55666 |
rs760933447 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637067 | CGCTCCAGCTTCGCC[A/C]GCCCGGCTCCGCCAG | 55666 |
rs760989644 | snp | A/C | 3.10227e-05 | 0.00393832 | missense, nc-transcript-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81559293 | CACATCTCGCAGTGG[A/C]CTGTGCCTGGCTGGT | 55666 |
rs760993996 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571044 | CCATCAATCTGTTTT[A/C]ATCTTAATTACACCC | 55666 |
rs761012760 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559620 | GCCTCCTGCACCACA[-/G]GGAGTAACAGGGAGC | 55666 |
rs761042511 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601062 | TAGCTTCGACTGGCT[-/C]CCATGCAACTGAAAC | 55666 |
rs761059032 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569820 | TTTGCACCTAAGATA[C/T]AATCAATAGATGCTA | 55666 |
rs761079402 | snp | A/G | 1.65905e-05 | 0.0028801 | synonymous-codon, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81589052 | ACGGACCAGTGCCAT[A/G]CACTGATTGGACACC | 55666 |
rs761085164 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621665 | AAACTGGCACCAACA[A/C]CACGACCTGGCTGTG | 55666 |
rs761088692 | snp | A/G | 4.83851e-05 | 0.00491836 | missense, intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81608773 | TAGGCGTGGAAGGAC[A/G]TGTGCTTCACGGGAG | 55666 |
rs761096563 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584604 | CTGGGAAAAGCCCAG[A/T]GAATGAGAAGGGCTG | 55666 |
rs761109164 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580012 | AGCCTCCTCTCCTGA[C/T]TCACCAGGGAGCTCC | 55666 |
rs761110385 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585675 | CTGGGGGGGGGGGGA[-/A]AGAAAGAAATCAGAG | 55666 |
rs761180343 | snp | C/T | 2.19556e-05 | 0.0033132 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606847 | AACTTAAACATCACA[C/T]TGGTGAAAAGTTGAG | 55666 |
rs761210595 | snp | A/C/T | 7.07139e-05 | 0.00594575 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81610221 | TCACCTCTAGAGGGA[A/C/T]GCAGTGCACGCATTT | 55666 |
rs761213947 | snp | G/T | 1.76201e-05 | 0.00296812 | missense, nc-transcript-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567462 | GAACAGCAAGAGGTG[G/T]AAATCTGAGATGGTA | 55666 |
rs761257247 | in-del | -/CAT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603881 | ATGTAAAATACACTA[-/CAT]CATTATACATAATTA | 55666 |
rs761262749 | snp | A/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562784 | TCTCTACAACAAATT[A/T]AAAAAATCAGCCAGG | 55666 |
rs761265190 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595631 | CTCACTGCAACCTCC[A/G]CCTGATGGGTTCAAG | 55666 |
rs761339184 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633071 | GGAGGCAGAGCTTGT[A/G]GTGAGCAGATCGCGC | 55666 |
rs761378084 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634087 | GTGTTGCCCAGGCTG[A/G]TCTCAAACTCCTGAG | 55666 |
rs761398678 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601267 | GTAAATTAGTGAAAA[C/T]CTGGCAAACCACAAA | 55666 |
rs761440215 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626861 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACCTGAG | 55666 |
rs761440913 | snp | C/G | 1.69507e-05 | 0.0029112 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608836 | GGCTGCCAAGACACA[C/G]AGTAAGCGAGTGCAG | 55666 |
rs761458657 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574366 | GAAAATAAAGGTGTT[C/G]TATCCCCCTTTCCTC | 55666 |
rs761486715 | snp | A/T | 4.86263e-05 | 0.0049306 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567554 | GGAATGGGAATAAAC[A/T]TGAATGTTCCATACA | 55666 |
rs761490925 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593341 | GAGGCCTGGACCCAG[C/T]CCTGTGCTCAGCCCT | 55666 |
rs761491212 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588759 | GGTGAGAAGCCCTAC[A/G]CCATGGAAGCATGAG | 55666 |
rs761634817 | snp | C/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638406 | TGGGTTCCAGTGATT[C/T]TCCTGCCTCAGCCTC | 55666 |
rs761644480 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558550 | GGATGTGGAAACTAG[C/T]CTCTCTCACTCCCCT | 55666 |
rs761742900 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626231 | TGAGCCAGGAAAACC[A/G]CTTGAACCCCGGAGG | 55666 |
rs761761122 | snp | A/C/G | 0.000133918 | 0.00818196 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622240 | TCTATTGATGTAAAC[A/C/G]GAGAAGCCATTATTT | 55666 |
rs761763328 | snp | A/G | 1.65553e-05 | 0.00287705 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600445 | GCAGGGAATCAAAGG[A/G]AGAAGATGGACTTAG | 55666 |
rs761771849 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572652 | CTGGGACTCCCCACT[-/G]GGAGAGCACATCAAA | 55666 |
rs761777816 | snp | A/C | 2.41929e-05 | 0.00347791 | missense, nc-transcript-variant, synonymous-codon | NPLOC4 | GRCh38.p7 | 17:81559372 | GTGTGGAGCCCCCGA[A/C]GGCGCCGTACTCATG | 55666 |
rs761786952 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576651 | AGAACGAAAACCTGG[A/C]GTGTGTTTGCAACAC | 55666 |
rs761840595 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558121 | CACGCCACAGAGGAA[C/T]GCAGAGCACACAAGC | 55666 |
rs761849002 | snp | C/G | 3.31367e-05 | 0.00407029 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622152 | TCCCTGCTTCCTCCT[C/G]AGAGGACACTTACTT | 55666 |
rs761872952 | snp | A/G | 1.65825e-05 | 0.00287941 | missense, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81589039 | GCAAACACTCATCAC[A/G]GACCAGTGCCATACA | 55666 |
rs762003150 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566739 | GTTCTGAGTCAGTGG[C/T]GGAGCAGCTCAGAAA | 55666 |
rs762040347 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621093 | GATGCAAAACCCTTC[A/T]AGAAAGAAAGAAAAG | 55666 |
rs762050657 | snp | A/C | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567902 | CCAACATGGCGAAAC[A/C]CCGTCTCTACTAAAA | 55666 |
rs762056391 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568033 | GTAGTGAGCCAAGAT[C/T]GCACCACTGCACTCC | 55666 |
rs762071616 | in-del | -/AAAAAAAAAAAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591456 | AAACAGAAAAAAAAA[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA | 55666 |
rs762124504 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560551 | GTCTCTACTAAAAAT[G/T]CAAAAATTACCTGGG | 55666 |
rs762132265 | in-del | -/A | 2.57619e-05 | 0.00358891 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606843 | AGCAACTTAAACATC[-/A]ACATTGGTGAAAAGT | 55666 |
rs762138196 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597083 | GCGCCACTGCACTCC[A/G]GCCTGGGCAAAAGAG | 55666 |
rs762141062 | snp | A/G | 0.000240414 | 0.0109612 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604567 | GGTGGCTCATAAATC[A/G]CAGCCACTTCAGCCC | 55666 |
rs762144983 | snp | A/G/T | 0.000148357 | 0.00861141 | synonymous-codon, intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81608784 | GGACATGTGCTTCAC[A/G/T]GGAGGCTCGAGATGG | 55666 |
rs762190667 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559613 | GAAAAATGCCTCCTG[C/T]ACCACAGGGAGTAAC | 55666 |
rs762209219 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609962 | CCCGCTGTAAATGCT[A/G]CCCCTTTATCACAGC | 55666 |
rs762219205 | snp | C/T | 1.66291e-05 | 0.00288345 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606740 | TTAGTACAGATGCCA[C/T]TCGGCCACGGGAGGT | 55666 |
rs762257101 | snp | A/G | 0.000150795 | 0.00868188 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565382 | GTTGCATTGCCGATG[A/G]CACCTGCCAGGATGC | 55666 |
rs762293019 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624217 | CGAGGTCAGGAGATC[A/G]AGGCCAGCCTGGCCA | 55666 |
rs762309308 | snp | A/C | 0.000226732 | 0.0106449 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636933 | TGCTCTCGGCCATGG[A/C]GGCTGCTCCTGCCTC | 55666 |
rs762376884 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630364 | AAAATCACAGCTTAC[C/T]GCAGCCTTGACATCC | 55666 |
rs762399470 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584826 | AACAAATGATAGGTA[A/G]GACCTCCACAGAGAA | 55666 |
rs762401959 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586886 | GGCTCTGACCAGCTA[C/T]TTGCCACCTGGATGG | 55666 |
rs762407260 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591950 | GCCCAGCCCAGTGTG[-/T]GGGGTAAGTTCTACA | 55666 |
rs762415000 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571222 | CCATCCAATTTCAAA[C/T]GCAGCCTGAATAGAT | 55666 |
rs762514826 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622755 | GGAGTTTCACCATGT[C/T]GGCCACGGTGGTCTC | 55666 |
rs762543154 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589778 | CAGGGCGGGAGGACT[A/G]CTTGAGCCCAGGAGT | 55666 |
rs762547695 | snp | G/T | 2.213e-05 | 0.00332634 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565636 | AAAGGAAGGTTCCTC[G/T]TCGCTGTGCCTAAGG | 55666 |
rs762577157 | in-del | -/ACACACACACACACACACACAG | | | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81564105 | CACACACACACACAC[-/ACACACACACACACACACACAG]ACACACACACACAAA | 55666 |
rs762590339 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634292 | AGGTGTGAGCCACCA[C/T]GCCCAGCCCAGAAAC | 55666 |
rs762590840 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564515 | AAAACCTCGGCTGGG[C/T]GTGGTGGCTCACACC | 55666 |
rs762593406 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601466 | GGGTTTTGCCATGTC[A/G]GCCAGGCTAGTCTTG | 55666 |
rs762611877 | snp | A/G | 1.99126e-05 | 0.0031553 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567525 | ATAGGTGGCCAAGCT[A/G]TGGAAGTCCTAGAGG | 55666 |
rs762637213 | snp | A/G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580688 | TTCTCTACCCGTTCC[A/G/T]CTGGGGTGGCCCACC | 55666 |
rs762642887 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583413 | AAAAGGAAACAAGAA[C/T]TCTACCAGATGCAAA | 55666 |
rs762659737 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568088 | TGTCTTCCAAAAAAA[-/AAA]AAAAAAAAAAAAAAA | 55666 |
rs762701886 | snp | C/T | 0.00015374 | 0.0087662 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81600389 | GACCACTTCAGCTTT[C/T]GGATCCTCAAGAAGC | 55666 |
rs762725507 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580061 | GGGCGCTATGCTCCT[A/G]CCCCTCCTCCCCAGC | 55666 |
rs762737271 | snp | A/G | 3.52379e-05 | 0.00419735 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81559271 | GCCCTAGGTCCTGGG[A/G]AGGCTGCACATCTCG | 55666 |
rs762782852 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626504 | AAGCCAGAGGTCAAC[A/G]AAGACGAGAAGACCA | 55666 |
rs762801036 | snp | C/T | 4.97137e-05 | 0.00498542 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622146 | CCCCATTCCCTGCTT[C/T]CTCCTCAGAGGACAC | 55666 |
rs762812982 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594760 | AACCTGGGCGAGAGC[A/G]AGACTCCGTCTCTAG | 55666 |
rs762815364 | snp | A/G | 3.92642e-05 | 0.00443064 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81600374 | GGCAGCAATTTCATC[A/G]ACCACTTCAGCTTTT | 55666 |
rs762876343 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634646 | GCTGGAGTGCAGTGG[C/T]GCAATCTGGGCTCAC | 55666 |
rs762882657 | snp | A/G | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638560 | ACCTGGGCCTCCCCA[A/G]AGTGCTGGGACTATA | 55666 |
rs762892885 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558226 | GGGAGGTCCCAAATG[A/G]CCCTCACAAGAGGCA | 55666 |
rs762988030 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560392 | CACTCCAGCCTGGGC[A/G]ACACAGCGAGACTCC | 55666 |
rs762994278 | snp | G/T | 4.66821e-05 | 0.00483103 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572131 | GAGCAAAGACGATCA[G/T]TAGTAATGATTTTCC | 55666 |
rs763014395 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578698 | GTGAGAATGCACTCA[C/T]TATCACTGAGAACAG | 55666 |
rs763024090 | in-del | -/T | 7.95513e-05 | 0.00630629 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610169 | TGTCTACCCGCAGCC[-/T]CCCCACACTGGCCCA | 55666 |
rs763082172 | snp | C/T | 6.64022e-05 | 0.00576166 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606715 | CAGCGTGATGGCGCT[C/T]GGCTGGCACTTAGTA | 55666 |
rs763112153 | snp | A/G | 0.000132793 | 0.00814733 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636883 | TGCTGCCTCATCCCG[A/G]CGTCCCCGCTCCCGC | 55666 |
rs763137117 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558606 | AAATAAATAAAAGTC[G/T]TCTGGGCAGGAATTA | 55666 |
rs763149318 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580240 | CACCCCGGGTGGTGC[C/T]TCTGCACTAGCACAT | 55666 |
rs763167816 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582867 | TGCACATAAAGCTCC[A/G]CAGCTGCAGGCTCTT | 55666 |
rs763188710 | snp | C/T | 1.68295e-05 | 0.00290077 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606641 | GCTCTTCTGGAAATA[C/T]CCGTTTCTCAGCCAT | 55666 |
rs763189798 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599449 | TTGAACCCAAATATG[C/T]CCCTAAATCAAGATG | 55666 |
rs763288383 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607331 | GAAGACTGTCAATGA[C/G]AAAATCCTGGACCCT | 55666 |
rs763324567 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631776 | TCTCTCTCATTTCCT[C/G]CATTACCATCTCTTG | 55666 |
rs763349442 | snp | A/C | 1.65616e-05 | 0.00287759 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81629791 | CACTCCATCCGGGGA[A/C]TGGACACGAATTATC | 55666 |
rs763354492 | snp | A/C | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561834 | ACACTTCTGGGCTAC[A/C]GTGTCCTCCAGCTTT | 55666 |
rs763393195 | snp | A/G | 0.000151688 | 0.00870751 | intron-variant, stop-gained | NPLOC4 | GRCh38.p7 | 17:81565367 | GCCGAGTCTCTACTC[A/G]TTGCATTGCCGATGG | 55666 |
rs763449135 | snp | C/T | 1.65647e-05 | 0.00287786 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81597265 | TTCGACTGTAGCGGA[C/T]GGTACCCTTTCGGGT | 55666 |
rs763483716 | snp | A/T | 2.69175e-05 | 0.00366852 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559435 | CAGGGTGGAAGAGAA[A/T]TGAGCACTCATCATT | 55666 |
rs763527262 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568177 | GTGGGCTGCGGGAGG[A/G]GCCTGGGGCCCCCTT | 55666 |
rs763533483 | snp | A/G | 3.4574e-05 | 0.00415762 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608678 | AAGCAACAACTGCCA[A/G]CTACACAAAAAGGAA | 55666 |
rs763590230 | snp | A/G | 5.03107e-05 | 0.00501526 | synonymous-codon, intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81608793 | CTTCACGGGAGGCTC[A/G]AGATGGTTTAGATAG | 55666 |
rs763638554 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599329 | GAGAAACTTGTGTCT[C/T]GCAGAAAATTATTTA | 55666 |
rs763642741 | snp | G/T | 1.84235e-05 | 0.00303503 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589123 | CAAGAGAGAGACCTT[G/T]AAAAAGAGTCTACCA | 55666 |
rs763647002 | snp | C/T | 2.00523e-05 | 0.00316635 | missense, nc-transcript-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567526 | TAGGTGGCCAAGCTA[C/T]GGAAGTCCTAGAGGA | 55666 |
rs763690108 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560826 | TTTTGCCTCCCACTC[A/G]CAAGGTACGAGAGTC | 55666 |
rs763707657 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633008 | GGTGGAGGGCGCCTG[C/T]AGTCCCAGCTACTTG | 55666 |
rs763728210 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598568 | CTGGGAGCTCCACCT[A/C]AAGGCCGGAAGGAAG | 55666 |
rs763728253 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612359 | AGAATTCTCTCACAC[A/T]CACACGCTCTCAAAA | 55666 |
rs763734897 | snp | C/G | 2.02403e-05 | 0.00318115 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81600413 | AAGAAGCTCCAAGCT[C/G]TTCTGTGTACCAATC | 55666 |
rs763774682 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573239 | ATTATAGGGCCTTAC[A/G]TAAAAGTTTACGTTT | 55666 |
rs763797243 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631985 | TCTTTTTTTTGAGAC[A/C]GTCTTTTTCCGTTGC | 55666 |
rs763822100 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580997 | TGGGCCAGCCCACCC[A/G]TGGGCTTATGCCCGT | 55666 |
rs763829549 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590398 | GGGCAGATGATGCCA[C/T]GGGGGCAGCCTGAGC | 55666 |
rs763896083 | in-del | -/CCT | | | cds-indel, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557190 | GAGGTGGGGCTGAGA[-/CCT]CCTTCCCACAAGAGG | 55666 |
rs763917347 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625159 | GACCAGGGGCAGGAA[C/T]GGAATGAGAGAAAGG | 55666 |
rs763919180 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591603 | TTATAAACAGCAAAA[C/T]TGGCCATATGGATAA | 55666 |
rs763963595 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637273 | GCTCGTCCTCGGAAA[C/T]CCAAGCGGCACAGGA | 55666 |
rs763993906 | snp | A/G | 6.37938e-05 | 0.00564737 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600324 | GCCCCCTGCTTGGCT[A/G]CCGGATGCCTCAGTA | 55666 |
rs764008925 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589363 | GTGAAACCCCGTCCC[C/T]ACTAAAAATAAAAAA | 55666 |
rs764064095 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566028 | TAGCCTTCCGAGTCA[A/G]ACTGCAGGGGATTAA | 55666 |
rs764065921 | snp | C/T | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556541 | CTTCCTGGGCTTTGT[C/T]CTTCACCTGCTGTTT | 55666 |
rs764105395 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575348 | CCTCATGATCCACCC[A/G]CCTTGGCCTCCCAAA | 55666 |
rs764119229 | snp | C/T | 1.67008e-05 | 0.00288965 | missense, upstream-variant-2KB, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613439 | GAACTGACGTCTCCA[C/T]TTCAGATGAGGGCCC | 55666 |
rs764160718 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624369 | GTTGCAGTGAGCCAA[G/T]ATGGCGCCATTGCAC | 55666 |
rs764185888 | snp | C/T | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636101 | CCTCAGCCTCCCAAG[C/T]ATCTGGGATTACAGT | 55666 |
rs764190771 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609147 | GCCTCTGCCTCCCAA[A/G]TAGCTAGGACTACAG | 55666 |
rs764194533 | snp | A/G | 2.40336e-05 | 0.00346644 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572136 | AAGACGATCAGTAGT[A/G]ATGATTTTCCTTTCA | 55666 |
rs764209099 | snp | A/G | 1.65636e-05 | 0.00287776 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613364 | CGTCCTGTTTGCTGA[A/G]GTACTGATCAATCTC | 55666 |
rs764228708 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576537 | ACTGAGGGGCAATTG[C/T]ACTTCCAAAGTACGA | 55666 |
rs764292939 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630237 | TACAAACATTAGACA[C/G]TCTTCAAGAGTCCTA | 55666 |
rs764298862 | snp | A/G | 1.95166e-05 | 0.00312376 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81572044 | ATACTCCACAGGCAG[A/G]GGCCGGGCCAGCTGG | 55666 |
rs764300545 | snp | A/C | 1.65941e-05 | 0.00288041 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606727 | GCTCGGCTGGCACTT[A/C]GTACAGATGCCATTC | 55666 |
rs764351486 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559071 | TGCAGAATACCAGCC[A/G]TGGCGCCCGCTCTCC | 55666 |
rs764366138 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617353 | TCACAGTTCACAACA[C/G]TGTGGACAAAGACCC | 55666 |
rs764384241 | snp | A/G | 1.65616e-05 | 0.00287759 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81629794 | TCCATCCGGGGACTG[A/G]ACACGAATTATCTGT | 55666 |
rs764414700 | snp | G/T | 0.000151573 | 0.00870421 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565369 | CGAGTCTCTACTCGT[G/T]GCATTGCCGATGGCA | 55666 |
rs764465669 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81635039 | TCTATAAAAAAATGT[G/T]TTTAATTAAAAAGAT | 55666 |
rs764466302 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607693 | CCTAGACTGAGAAAG[A/G]CTGACCAAGTCTCTT | 55666 |
rs764587609 | snp | A/C | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562696 | GCTTACCACTGCAAT[A/C]TCAGCACTGAGGCGG | 55666 |
rs764612215 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568829 | TTAGCCTTTGTGGCC[A/G]TCCATCACCTAGCCA | 55666 |
rs764653543 | snp | A/G | 2.78718e-05 | 0.00373298 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559441 | GGAAGAGAAATGAGC[A/G]CTCATCATTTCTGGC | 55666 |
rs764723924 | in-del | -/TG/TTG | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635990 | TTTTTTTTTTTTTTT[-/TG/TTG]GAGACGCAGTCTCGC | 55666 |
rs764783455 | snp | A/G | 1.66885e-05 | 0.00288859 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606752 | CCATTCGGCCACGGG[A/G]GGTGCCCCTCGCACC | 55666 |
rs764785813 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587970 | ATGAGCCGCCGCGCC[C/T]GGCCGAAAAAAGTTA | 55666 |
rs764794458 | snp | C/T | 3.51735e-05 | 0.00419351 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600312 | GAGCCTGGCCACGCC[C/T]CCTGCTTGGCTGCCG | 55666 |
rs764798068 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634315 | CCAGAAACTTTTCAA[A/G]AGATCTCTTTCTTAA | 55666 |
rs764801363 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597372 | TAGACGATGAATGGC[C/T]GGGCGCAGTGACTCA | 55666 |
rs764840729 | in-del | -/TTTT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630291 | TTTTCTAATTGTTAC[-/TTTT]TTTTTGCTTTTTTGA | 55666 |
rs764844392 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604383 | TGAAGGTTTTAGGAG[A/C]CATGATCTCACTCTC | 55666 |
rs764865616 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620977 | GCAGTGAGCTACGAT[C/T]GCACCACCGCACTCC | 55666 |
rs764870148 | snp | C/T | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556430 | AGCACTTGTTCTAGA[C/T]GCTTTCTGTTGTCAC | 55666 |
rs764873357 | snp | A/G | 0.000179931 | 0.0094833 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636965 | GGGCTCGAGCCCCGG[A/G]CCGCCGCCGCCTGCC | 55666 |
rs764901816 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562847 | CAGGAGGCTGAGGCG[A/G]GAGGATTGTTTGAGC | 55666 |
rs764913218 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621795 | GCCACTGCAGTGGCA[A/G]CACTCCTACCCAAGC | 55666 |
rs764979778 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579139 | TAGCACTTTGGGAGG[C/G]AAGGCAGGTGGATTA | 55666 |
rs765026311 | snp | C/T | 1.65636e-05 | 0.00287776 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81597299 | TTCTGAGACGAGGTC[C/T]GTAAATATCCAGCCA | 55666 |
rs765054303 | snp | A/G | 7.42198e-05 | 0.00609134 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610284 | TACAAGGCAGAAAAA[A/G]GCAGAGCAGTGAGGA | 55666 |
rs765185387 | snp | A/G | 2.43989e-05 | 0.00349268 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572009 | AGCTGTGCATGGGGG[A/G]CACTTACGTCTATGA | 55666 |
rs765191176 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577604 | AGTCTGAAAAGGGAA[C/G]TATTGGCCTGTATCT | 55666 |
rs765207099 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572471 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGTCC | 55666 |
rs765223607 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626271 | CAGTCAGCCAAGATC[A/G]CGCCACTGCACTCCA | 55666 |
rs765231711 | snp | G/T | | | synonymous-codon, nc-transcript-variant, missense | NPLOC4 | GRCh38.p7 | 17:81559388 | GGCGCCGTACTCATG[G/T]AGACCTGGGAGCTGC | 55666 |
rs765274170 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559727 | TGGGTTGTTTCCAGC[-/T]TTTTTTTTTTTTTTT | 55666 |
rs765285998 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612531 | TTATGGCTCTCTGAT[C/T]TAAGACATAAAAGTT | 55666 |
rs765289945 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614250 | CCACTGCACTCCAGC[C/G]TGGTGACAGAGGGAG | 55666 |
rs765364873 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591883 | CAGATCCCCAGCAAG[A/T]AATTTTAACAGCCCG | 55666 |
rs765392677 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557630 | CAGGACCAGAGGAGA[C/G]AGCAGAGGACAAAAC | 55666 |
rs765400142 | snp | A/T | 1.65888e-05 | 0.00287996 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81569053 | CGGTTTTCAATAGGA[A/T]ATGGATTTTGCGAAA | 55666 |
rs765408341 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576853 | TCCTTGCCAGAGTCA[C/T]GGGCGCGAGGGCAAG | 55666 |
rs765427875 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576652 | GAACGAAAACCTGGC[A/G]TGTGTTTGCAACACA | 55666 |
rs765447643 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623282 | CGACACCAGCCTGGT[C/T]AACATAGTGAAACCG | 55666 |
rs765478388 | in-del | -/AC | 6.04102e-05 | 0.00549558 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608831 | CGAATGGCTGCCAAG[-/AC]ACAGAGTAAGCGAGT | 55666 |
rs765502204 | snp | G/T | 0.00692033 | 0.0584147 | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637452 | GATCACACCTTCATG[G/T]TTTTTTTTTTAAGTA | 55666 |
rs765526513 | snp | A/G | 5.01065e-05 | 0.00500507 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622313 | ACAGAAATTTAATGA[A/G]ATGCTAAAGTATCAC | 55666 |
rs765593827 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614887 | TGCTGCCAACAAGAC[-/AC]ACACACACAGGGGAC | 55666 |
rs765624796 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597143 | ATAAATAATGGGGCC[C/T]GAAAGCTAGAACCAG | 55666 |
rs765659882 | snp | C/G | 2.58937e-05 | 0.00359808 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559427 | TGTGCCTGCAGGGTG[C/G]AAGAGAAATGAGCAC | 55666 |
rs765719786 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559139 | AGCCCAGGACAGCCA[A/G]CCCCTTGTTCCTCCA | 55666 |
rs765720187 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630370 | ACAGCTTACTGCAGC[C/T]TTGACATCCAAGGTT | 55666 |
rs765730841 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585111 | GGAGGCGGAGGTTGC[A/C]GTGATCTGAGATCGC | 55666 |
rs765740346 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631751 | CTGATGGTGCATTCT[A/G]TAGCTTCTTTCTCTC | 55666 |
rs765749847 | snp | C/T | 2.26257e-05 | 0.00336338 | missense, nc-transcript-variant, synonymous-codon | NPLOC4 | GRCh38.p7 | 17:81559378 | AGCCCCCGACGGCGC[C/T]GTACTCATGGAGACC | 55666 |
rs765822546 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621925 | CAAAGACAATAACTT[C/T]CTCCTCAGTGACACA | 55666 |
rs765824295 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580509 | CAGCTTCCAAGGGCC[C/T]CTCCCACCTCTACCC | 55666 |
rs765837795 | snp | A/G | 1.65652e-05 | 0.0028779 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596152 | ACTTGGATCCAAAAT[A/G]TCCGTCTGGAGAGAG | 55666 |
rs765884304 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636287 | ACAATTTCAATTTCA[A/G]GTAAAAAGTGAAATC | 55666 |
rs765905474 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586891 | TGACCAGCTACTTGC[A/C]ACCTGGATGGAGATG | 55666 |
rs765976194 | snp | A/G | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637841 | CGGGAGTCTGAGGCC[A/G]GAGAATCTCTTGAAG | 55666 |
rs765996774 | snp | C/T | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635752 | AACTGCAGAGACTGT[C/T]ACAATGCTACAGTAT | 55666 |
rs766013318 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607928 | AGCCACCATCTCCTC[A/G]TTGCACTGACAGGAA | 55666 |
rs766015694 | snp | C/T | 4.97938e-05 | 0.00498943 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613330 | TACAGCTGTGGGTCT[C/T]GGCTTCTGTAAATCT | 55666 |
rs766035484 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608973 | GGTCTCCCTTACCAC[C/T]CTGAGTCAGAACCAA | 55666 |
rs766099522 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614940 | AGCTCTAAACCAACA[C/T]GGTGAAGGAAGAGCA | 55666 |
rs766104710 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628934 | CCCAGGCTGGAGTGC[A/G]GTGGCGCGATCTCAG | 55666 |
rs766105670 | snp | A/C | 6.89489e-05 | 0.00587109 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81610238 | CAGTGCACGCATTTC[A/C]CCAAAGGGCCGTGGC | 55666 |
rs766106515 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605824 | AACAAACACATTTTC[-/T]TTTTTTTTTTTTTTT | 55666 |
rs766118860 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576364 | GCAGACTTTTTTCAA[C/G]CAAACACAGATTGAA | 55666 |
rs766119383 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622801 | GGTGATCCGCCCACC[C/T]TGGCCTCCCAAAGTA | 55666 |
rs766133866 | snp | A/C/G | 2.59757e-05 | 0.00360377 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600456 | AAGGGAGAAGATGGA[A/C/G]TTAGAGCAGAGGGCT | 55666 |
rs766178333 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573588 | TTCCTCACTATTGTA[C/T]TTGACTAGTCTTAAA | 55666 |
rs766183481 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563247 | GCCCAGCTAATTTTT[A/G]TAGTTTTAACAGAAA | 55666 |
rs766247945 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638635 | TAATTTGGTGGGTAT[-/G]GGGTCAGAAAGTAGG | 55666 |
rs766287973 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601499 | CTCCTGGCCTCAAGT[A/G]ATCTGCCTTGCCCCT | 55666 |
rs766307359 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558054 | ATCATTAAGGCAAAG[A/C]AGCATCGAGATGCCC | 55666 |
rs766318094 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575276 | GCTAATTTTTTTCTA[-/T]TTTTTTAGTAGAGAC | 55666 |
rs766321073 | in-del | -/A | | | intron-variant, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563589 | AGGGAAACAAAAAAG[-/A]AAAAAAAAAAAAAGA | 55666 |
rs766323971 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583448 | AGTTATCATTAAATA[C/T]GTTTTCTTCATGTTT | 55666 |
rs766328528 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588126 | GATGAGACACTGTAG[A/G]AGTCCAGATCAACGA | 55666 |
rs766349893 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558629 | AGGAATTACTGATAA[C/G]TGTTATTATAACCAA | 55666 |
rs766473301 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633066 | ACCCAGGAGGCAGAG[C/G]TTGTGGTGAGCAGAT | 55666 |
rs766481491 | in-del | -/C | 1.6863e-05 | 0.00290365 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610194 | GGCCCAGAACTTACT[-/C]CGCAGAGACTCTCAC | 55666 |
rs766481614 | snp | C/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638578 | TGCTGGGACTATAGA[C/T]GTGAGCCACCGTGCC | 55666 |
rs766494140 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634826 | CTGACCTCGTGATCC[A/G]CCCACCTCGGCCTCC | 55666 |
rs766508463 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605543 | ATCCCAGCTACTCCG[C/G]AGGCTGAGGCAATAG | 55666 |
rs766510328 | snp | C/T | 2.6515e-05 | 0.00364099 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600458 | GGGAGAAGATGGACT[C/T]AGAGCAGAGGGCTCA | 55666 |
rs766533837 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567026 | TGATTTAGGAGGAGG[C/G]GAGATATGAGTAAAA | 55666 |
rs766562337 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81559486 | CAGAGTGTGGGCATG[A/G]GGGCAGGGGCAGGCA | 55666 |
rs766592208 | snp | G/T | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622182 | TGATTTTTAGCAAGT[G/T]GAGGGATTTGTTGGA | 55666 |
rs766598914 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592022 | AAAGCGCACACTTCA[C/T]TGGGGCTCTTATACT | 55666 |
rs766605718 | snp | C/G | 6.11266e-05 | 0.00552807 | missense, nc-transcript-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81559296 | ATCTCGCAGTGGCCT[C/G]TGCCTGGCTGGTTCA | 55666 |
rs766654966 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615765 | AAGGACGCCTGAACA[A/G]CTGTGAAAAACCCAC | 55666 |
rs766688128 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578438 | TAACACCTGACCCAC[A/G]GGAAGCTCTCAACAG | 55666 |
rs766689679 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599032 | GGTGGCTCACGCCCA[C/T]AATCCCAGAACTTTG | 55666 |
rs766693875 | snp | C/T | 1.6607e-05 | 0.00288153 | missense, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81589059 | AGTGCCATACACTGA[C/T]TGGACACCTGGTACC | 55666 |
rs766803057 | snp | C/T | 1.6577e-05 | 0.00287893 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596125 | TTATACCTGTAGCCA[C/T]TGCAGTAACAAACTT | 55666 |
rs766806698 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585280 | ATTCCTGGAGATGAC[C/T]GACGACAGAGAAGCA | 55666 |
rs766857382 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599487 | CTTGTTAGAAACAGG[A/G]TGTTTCTTTCCTAAA | 55666 |
rs766866569 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620062 | AACTCTACAGGTCAA[C/T]GGACCAAGTTCCTCA | 55666 |
rs766928968 | snp | C/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560770 | ATTGTGTGCTGAACT[C/T]TCTAAGACCCTGAGA | 55666 |
rs766964379 | snp | G/T | 1.65641e-05 | 0.00287781 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596161 | CAAAATGTCCGTCTG[G/T]AGAGAGCCGGCACAT | 55666 |
rs766988161 | snp | A/C | 2.15841e-05 | 0.00328505 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606855 | CATCACATTGGTGAA[A/C]AGTTGAGCAAGAGGC | 55666 |
rs766992582 | snp | A/C | 1.66407e-05 | 0.00288446 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596281 | CAAATTTTACAGCAT[A/C]ATGCCAAAATATACT | 55666 |
rs767007635 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557286 | TAGCTCTGACTCTCT[C/T]TGGACAATAAAATAA | 55666 |
rs767038840 | snp | A/G | 1.67424e-05 | 0.00289326 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81610227 | CTAGAGGGACGCAGT[A/G]CACGCATTTCCCCAA | 55666 |
rs767047018 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570771 | GCGCCTGTGGCCCAG[A/G]GCTGGGCATGGAGCT | 55666 |
rs767065919 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81610246 | GCATTTCCCCAAAGG[A/G]CCGTGGCGGCATCTG | 55666 |
rs767219818 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608895 | TGAGCCTCTGCTACG[C/T]ACAGGGGGAGGCCAG | 55666 |
rs767241021 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603404 | AGTTCAAGACCAACC[C/T]GGGCAATATAGCGAG | 55666 |
rs767326927 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601841 | CACACATTTGTGCAG[A/G]GGCCACTAGCAAGCC | 55666 |
rs767344005 | snp | C/G | | | intron-variant, missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81589113 | GGACCACCTGCAAGA[C/G]AGAGACCTTTAAAAA | 55666 |
rs767370500 | snp | A/C | 1.65886e-05 | 0.00287993 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81569025 | GCTCACCTGTGTCTC[A/C]CCCAATACATCCCGG | 55666 |
rs767433306 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590140 | ACGGCCGCCACACAG[A/T]GTTAATGCCACCAGG | 55666 |
rs767480962 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558903 | GAAAATAAAGAGAAG[A/G]CTGGGTGGTGGCAGC | 55666 |
rs767511239 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631366 | CCTGGCCAACACAGC[A/G]AGACCCCATCCTAAT | 55666 |
rs767528006 | snp | C/T | | | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565023 | TCGTTCAGGACCTGG[C/T]GACTGAGGGTCCGGA | 55666 |
rs767533743 | in-del | -/G | 1.65636e-05 | 0.00287776 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613370 | GTTTGCTGAGGTACT[-/G]ATCAATCTCATCCTC | 55666 |
rs767546189 | snp | C/T | 2.48327e-05 | 0.0035236 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600452 | ATCAAAGGGAGAAGA[C/T]GGACTTAGAGCAGAG | 55666 |
rs767552587 | snp | C/T | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635872 | CAGTTAGTTTTTTTC[C/T]CATCACATTTACTTT | 55666 |
rs767605501 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629138 | CCGCCTCGGCCTCCC[A/C]AAGTGCTGCGATTAC | 55666 |
rs767634091 | snp | C/G | 2.92505e-05 | 0.00382418 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600328 | CCTGCTTGGCTGCCG[C/G]ATGCCTCAGTACCTT | 55666 |
rs767652273 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583506 | ACAAGAAAGGTGAAA[C/G]AGAAAAGCCCCACGT | 55666 |
rs767652774 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626742 | AGTCAAGGCTGCAGT[A/G]AGCTGTGACTTTGCC | 55666 |
rs767678295 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614885 | ACTGCTGCCAACAAG[-/AC]ACACACACACAGGGG | 55666 |
rs767703662 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574760 | GGCTCATGCCTGTAA[A/T]CCCAGCGCTTTGGGA | 55666 |
rs767706580 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606165 | AGGAATAGAGAATAG[C/G]AGGTTTCCAAAAAAG | 55666 |
rs767714845 | snp | C/G | 1.77483e-05 | 0.0029789 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588906 | CAGGTTCACACCATT[C/G]TCCATGTACAGAGTT | 55666 |
rs767729099 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81579077 | AGGTGCACACAGCAT[A/G]GACTGCATGCATTAC | 55666 |
rs767751691 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592829 | CTCTACAAAAAATAC[-/A]AAAAATTGGCCGGGT | 55666 |
rs767804475 | in-del | -/GTT | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636343 | AAGAGGAATTGTCAA[-/GTT]GTCCTTCCAAGTAAG | 55666 |
rs767843357 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613822 | CCTCCCGCCTCTCAC[C/T]CTCTGCTTGGCCCCC | 55666 |
rs767853206 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584203 | TTTGCTTTTACAGTT[C/T]TCTTTGCTCCAACTG | 55666 |
rs767857692 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560519 | GGAGACCATCCTGGC[C/T]AACATGGTGAAACCC | 55666 |
rs767893005 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593775 | GACATGAGCGCCTTT[A/G]TTCTCTGCTCCCCTC | 55666 |
rs767970131 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578008 | GCTGTCAGCACCTGT[C/G]CACTGCCTCTCCTAC | 55666 |
rs767978660 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624940 | GCAGACAGGGCCGTG[C/G]GAAGCCACACAGACG | 55666 |
rs767983198 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627859 | GAGAACTGCTGGAAC[C/G]CAGGAGGCGGAGGTT | 55666 |
rs768007546 | snp | C/T | 1.69415e-05 | 0.00291041 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569139 | AACACAAACCCATGA[C/T]AAATGAGGCTGAAAA | 55666 |
rs768022898 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603807 | CTAAATAGTACAGCA[A/T]GCATATCATTAACTA | 55666 |
rs768054249 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607660 | AAACACGCCCCCACT[A/G]GAGACTGTGTTCCTT | 55666 |
rs768056872 | snp | A/T | 1.75517e-05 | 0.00296236 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567468 | CAAGAGGTGGAAATC[A/T]GAGATGGTATCCAAG | 55666 |
rs768079082 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574793 | CCGAGGTGGGCAGAC[A/G]GCTTGAGGTCGGGAG | 55666 |
rs768108432 | snp | A/G | 0.000484496 | 0.0155568 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636934 | GCTCTCGGCCATGGC[A/G]GCTGCTCCTGCCTCC | 55666 |
rs768140614 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574350 | CTTTTCCACTCCCCA[A/T]GAAAATAAAGGTGTT | 55666 |
rs768146118 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613189 | AGTTTAATCTGAAGA[C/T]AGTAAAACTTAAGAC | 55666 |
rs768181191 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614094 | ATCCTGGCCAACAGG[A/G]TGAAATCTCGTCTCT | 55666 |
rs768200721 | snp | C/G/T | 3.31347e-05 | 0.00407019 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629823 | GTTGCAAACAAAACA[C/G/T]GATGGTTACTGCACA | 55666 |
rs768206618 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599778 | AAAAAGGAAATCCTT[G/T]TCTCATCTTCTAACT | 55666 |
rs768208095 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582673 | CTTCCAAAGTGCTGG[C/G]ATTACAAGTGTGAGC | 55666 |
rs768234115 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626073 | AGAATCGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 55666 |
rs768258643 | snp | C/T | 3.35121e-05 | 0.00409328 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568992 | AGTTACCTTAAATTA[C/T]GTTTCTAAAGACAAA | 55666 |
rs768346457 | snp | G/T | 1.81477e-05 | 0.00301223 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604543 | TTGAATCCCGTCATG[G/T]TTACCTGAGGTGGCT | 55666 |
rs768390030 | in-del | -/CTGTCT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564452 | CAATAGAGTGAGACC[-/CTGTCT]CTGTCTCTACAAAAA | 55666 |
rs768395040 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594173 | CCAGCTACTCGGGAG[A/G]CTGAGGCAGGAAAAT | 55666 |
rs768415045 | in-del | -/AAAG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595975 | GAATTTTTACCATAA[-/AAAG]AAAGGAGGAATTTAT | 55666 |
rs768477702 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593081 | CTGTTCCATATCCCA[A/C]AAGACTCTGAATGCC | 55666 |
rs768482915 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616189 | AGCCGGGGGTGGTGG[C/T]GGGCACCTGTAATCC | 55666 |
rs768496713 | snp | C/T | 4.90713e-05 | 0.00495311 | missense, nc-transcript-variant, synonymous-codon | NPLOC4 | GRCh38.p7 | 17:81559369 | TGTGTGTGGAGCCCC[C/T]GACGGCGCCGTACTC | 55666 |
rs768503208 | snp | A/C/G | 0.00013389 | 0.00818099 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622238 | TTTCTATTGATGTAA[A/C/G]CCGAGAAGCCATTAT | 55666 |
rs768547703 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558010 | TGGGCCAGCCTCTCC[C/T]GTGGGTGCAGAGCAG | 55666 |
rs768584239 | in-del | -/AC/ACAC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602986 | TACACAAATACACAC[-/AC/ACAC]ACACACACACACACA | 55666 |
rs768600597 | snp | A/C | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613778 | TTGCACACACAGCCA[A/C]AATGGACCTGCTGGG | 55666 |
rs768604817 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620527 | TAAAAAAATGCAAAC[C/T]GGTGATTACTGTTAG | 55666 |
rs768637492 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558481 | ACTGACTGGTGCCCC[C/T]GTCCACACTCATCAC | 55666 |
rs768650587 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622540 | GACTTTGAAGCAAAC[-/A]AAGAGTTAATGGCTA | 55666 |
rs768676970 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598837 | TCCACCCCCAGCAGA[C/G]ATGACTAGCCCACTG | 55666 |
rs768743032 | snp | C/G | 6.81733e-05 | 0.00583798 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608719 | ACCAGGTTACAGCAA[C/G]TTGCTTACTTGTCAG | 55666 |
rs768745665 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566648 | AACTAGCAGGATACA[A/G]GAACAGCTATAGGCT | 55666 |
rs768750931 | snp | G/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561297 | ACCCTCCGCCCAGCT[G/T]CTTCTTCTGCTTTCT | 55666 |
rs768772169 | snp | A/G | 1.94105e-05 | 0.00311526 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567423 | GACACGCACCTGCAG[A/G]GGCATAACTTCATTG | 55666 |
rs768829106 | in-del | -/AAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605280 | GCAAAACTCCATCTC[-/AAA]AAAAAAAAAAAATAA | 55666 |
rs768922523 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587967 | GGCATGAGCCGCCGC[A/G]CCCGGCCGAAAAAAG | 55666 |
rs768923275 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622652 | ACATCCCAGGTTCCA[C/G]TGATTCTCCTGCCTC | 55666 |
rs768978833 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617212 | AAACCAGGAGCCACA[C/T]GGCCCCTGTGAGTAC | 55666 |
rs768996359 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624203 | AGGTGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 55666 |
rs769010470 | snp | G/T | 1.90398e-05 | 0.00308538 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636885 | CTGCCTCATCCCGGC[G/T]TCCCCGCTCCCGCCC | 55666 |
rs769051325 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571062 | CTTAATTACACCCTA[C/G]GTAGTCTAAAAACCA | 55666 |
rs769103583 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580657 | TCAGGACTCGACCCA[C/T]CAGGGCACTCCAAGC | 55666 |
rs769139095 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609906 | CACGGAGGCCGACAG[C/G]CTCAGCTTTGTGTCA | 55666 |
rs769169400 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81556903 | TGCTTCAGGCGCTTT[A/T]ATTAGGTTCCACTGC | 55666 |
rs769173874 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606012 | TTTTTAGTAGAGATG[A/G]GGTTTCACCATATTG | 55666 |
rs769189919 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637451 | GATCACACCTTCATG[-/T]TTTTTTTTTTTAAGT | 55666 |
rs769208326 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628484 | TGCCACTGCACTCCA[A/G]CCTGGGCAACAGAGT | 55666 |
rs769273812 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564410 | GGCTGCAGTGAGTTA[C/T]GATTGTGCAACTGCA | 55666 |
rs769276466 | in-del | -/AAG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625483 | AGAAACAAATCATAA[-/AAG]AACAATCAAATGGAA | 55666 |
rs769297405 | snp | C/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635581 | GTCGCCCAGGGTGGA[C/G]TCCAGTGACGCCACC | 55666 |
rs769329864 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602602 | CGCTATTCAGGAGGC[C/T]GAGGCAGGAGAATCA | 55666 |
rs769377555 | in-del | -/AGTT | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635858 | TCCTGTCCAATGGTC[-/AGTT]AGTTTTTTTCCCATC | 55666 |
rs769379860 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574455 | AGCCAATCCCTAGGC[C/T]TACACACCATTTTAA | 55666 |
rs769380609 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614584 | GTTTCTGCTTGTCTC[C/T]GAAGCTACTGACGTA | 55666 |
rs769398787 | snp | A/G | 1.92914e-05 | 0.00310569 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81600383 | TTCATCGACCACTTC[A/G]GCTTTTGGATCCTCA | 55666 |
rs769446676 | snp | C/T | 0.000198748 | 0.00996667 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559257 | AGCAGAGGGCAGGCG[C/T]CCTAGGTCCTGGGGA | 55666 |
rs769468086 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575527 | GAGCCACTTCGTCCT[C/T]ACAAACACACTGGTC | 55666 |
rs769493668 | in-del | -/TTC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595956 | TATGCTGTTAAGTTG[-/TTC]AGAATTTTTACCATA | 55666 |
rs769555683 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576137 | TTTACAATGAACAGT[C/G]GGACTAGGTCAACCA | 55666 |
rs769578948 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568089 | GTCTTCCAAAAAAAA[-/AA]AAAAAAAAAAAAAAA | 55666 |
rs769624650 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583365 | ATTTATTCTCCATAA[C/T]TACAAGTCTTTGTTT | 55666 |
rs769639792 | in-del | -/AATTGATTA | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638077 | ATGTTAAATTACATT[-/AATTGATTA]AATTATGTTAGTAAT | 55666 |
rs769662724 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619490 | GGGGGGCAGAGGTTG[G/T]GGTGAGCTGAGACCA | 55666 |
rs769701879 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636733 | GGAGGGACACGGACG[A/G]GAAGCAGCCGAGGGG | 55666 |
rs769723633 | in-del | -/CAT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574960 | CCATTGATTGAATGG[-/CAT]CAACCCTGCTTTAGA | 55666 |
rs769755034 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607300 | TCTGCTTTAGGCTAA[A/C]ATAAAAACTACTGTT | 55666 |
rs769780018 | snp | A/G | 2.12177e-05 | 0.00325705 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572113 | TCAGAGGGGAACAGC[A/G]GTGAGCAAAGACGAT | 55666 |
rs769809433 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600008 | ACAGAGGAGCCAGCA[C/G]GGGTGCGGCTGGGGT | 55666 |
rs769821983 | snp | C/T | 1.66054e-05 | 0.00288139 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606711 | TGTTCAGCGTGATGG[C/T]GCTCGGCTGGCACTT | 55666 |
rs769824251 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587048 | TAACAAGGACAGACA[G/T]ACAGACGGTCCACGG | 55666 |
rs769877171 | in-del | -/AAAAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628225 | CATAAAAAAAAAAAG[-/AAAAA]AAAAAGAAAAAGAAA | 55666 |
rs769905988 | snp | G/T | 1.90112e-05 | 0.00308306 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636872 | GCCGGCAAATCTGCT[G/T]CCTCATCCCGGCGTC | 55666 |
rs769909751 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585935 | CAGAAGTTGCAACAA[A/G]CTGAGATCACGCCAC | 55666 |
rs769931028 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620670 | TACGTATTTTGTTTA[A/G]TAATTAAAAAGAGGA | 55666 |
rs770015719 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578585 | CTTACAAGCATGACA[C/G]GAGGGGAAGGGGAAG | 55666 |
rs770052601 | snp | G/T | 3.50576e-05 | 0.00418659 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81565549 | TCAGACCTCTTCCAT[G/T]TCTGGGCGAGCTCCT | 55666 |
rs770099878 | in-del | -/AT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603667 | TTACAGTGAATACTC[-/AT]ATACCCACCACTAGA | 55666 |
rs770132066 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621432 | CAGGTCCCAGGCCCA[A/C]CACTGAGCCAGTGGC | 55666 |
rs770133947 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612265 | GGGTCAGAATTCTTA[C/G]ATGCGTATGAGCCCT | 55666 |
rs770230584 | snp | C/T | 3.31268e-05 | 0.00406968 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81597256 | TCACCTTATTTCGAC[C/T]GTAGCGGACGGTACC | 55666 |
rs770246438 | snp | G/T | 1.68069e-05 | 0.00289882 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613287 | TTAAGATCACCACAA[G/T]TAGGACCCTGGAATC | 55666 |
rs770319415 | snp | C/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81566531 | GCAGGAGGTGCAGTT[C/T]CCTGGGCTGACTAGG | 55666 |
rs770379964 | snp | A/C | 3.64571e-05 | 0.00426933 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600306 | CCAACAGAGCCTGGC[A/C]ACGCCCCCTGCTTGG | 55666 |
rs770388167 | snp | G/T | 8.29717e-05 | 0.00644042 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622127 | TCATGGGGACCTCAT[G/T]TCCCCCCATTCCCTG | 55666 |
rs770398487 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81556957 | AATCCAAGCCCAGTG[A/G]TGCACACCTGTGAGC | 55666 |
rs770415606 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613253 | AGACATGTTATAAAT[A/G]TTTCCCTTTATTCAC | 55666 |
rs770463321 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636286 | GACAATTTCAATTTC[A/G]GGTAAAAAGTGAAAT | 55666 |
rs770464357 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624221 | GTCAGGAGATCGAGG[A/C]CAGCCTGGCCACCTT | 55666 |
rs770465923 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602885 | CTCCACACACACTAT[A/G]TATGTATATACACAT | 55666 |
rs770472555 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633785 | CCTCGGTTCACTGCA[A/G]CCTTTGCCTGCCGAG | 55666 |
rs770476273 | snp | C/T | 1.66032e-05 | 0.0028812 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613419 | AAAGACTTTGAAGCC[C/T]GGTGGAACTGACGTC | 55666 |
rs770491716 | in-del | -/A | 1.74379e-05 | 0.00295273 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588931 | AGAGTTCTTTTTCTT[-/A]CCATACTTTTACCTT | 55666 |
rs770492582 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557908 | AGAAGCCAACAGGCA[A/G]ATGTTCTCTGTTCAT | 55666 |
rs770494844 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591290 | AAATATAAAAATTAA[C/G]TGGGCATGGTGGCGT | 55666 |
rs770525932 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586151 | ATCCAAACCAGATAA[G/T]AAGACCCCCAGCAAA | 55666 |
rs770538312 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576216 | ATCATGCATAAATGG[A/T]TTATGGATCTCAAAA | 55666 |
rs770568848 | snp | C/T | 3.31466e-05 | 0.0040709 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629837 | ATGATGGTTACTGCA[C/T]AGCCTAGTGAGGTCC | 55666 |
rs770593213 | snp | A/G | 2.06217e-05 | 0.00321099 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572105 | TGCAATAGTCAGAGG[A/G]GAACAGCGGTGAGCA | 55666 |
rs770634302 | snp | C/G | 1.67514e-05 | 0.00289403 | missense, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81588961 | TATAAAACACATCAG[C/G]CACGTACTGCTCACT | 55666 |
rs770636858 | snp | A/G | 5.07756e-05 | 0.00503837 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559233 | GCTGGGCTGGGCCCG[A/G]TCCTAGCCAGCAGAG | 55666 |
rs770642872 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565827 | CCAAATAGGCCCAAG[C/T]GGGCATCTGTGCCTC | 55666 |
rs770771861 | snp | C/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636657 | CAGTCCATTCTCCCT[C/G]CTTAGAAAGGCTCGG | 55666 |
rs770784801 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570486 | CACGTGCTAGTGAGT[C/G]AGCTAGTGGGACTGA | 55666 |
rs770841908 | snp | C/T | 1.65737e-05 | 0.00287864 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629840 | ATGGTTACTGCACAG[C/T]CTAGTGAGGTCCTGA | 55666 |
rs770894633 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596551 | AACCTGTGCAACACA[C/G]CAAGACTCTGTCTCA | 55666 |
rs770930112 | snp | C/G | 3.3123e-05 | 0.00406945 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81629770 | CTTTGTTGCTGTGAT[C/G]CGCTTCACTCCATCC | 55666 |
rs770944554 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621470 | CATGCAACCTGCAGC[A/G]TCGAGAGGAAAACTG | 55666 |
rs770947332 | in-del | -/TATAT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595531 | ATATACATATATATA[-/TATAT]TTTTTTTTTCTTTTC | 55666 |
rs770977635 | snp | G/T | 2.40613e-05 | 0.00346844 | synonymous-codon, nc-transcript-variant, missense | NPLOC4 | GRCh38.p7 | 17:81559412 | GAGCTGCCCGCCAAC[G/T]GTGCCTGCAGGGTGG | 55666 |
rs771016595 | snp | A/G | 0.00182593 | 0.0301601 | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81565292 | CTGTGTACCTAAGAC[A/G]TACGGCCTGGACAAC | 55666 |
rs771178471 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608352 | GGGACAGCCTCTGTC[C/T]GATACTGCACTGTGG | 55666 |
rs771195231 | snp | C/G | 1.65712e-05 | 0.00287843 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597225 | ATAGGGCCACACGCA[C/G]AGTCCTGTCTCCACC | 55666 |
rs771272937 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595112 | TGTTGCCCAGGCTGG[C/T]CTCAAACTCCCAGTC | 55666 |
rs771276530 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600176 | GTTATTGGTGCCCAA[C/G]AAACATATGTGAAGT | 55666 |
rs771285286 | snp | A/G | 1.65743e-05 | 0.00287869 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596231 | CTCTTCTGAACTTAG[A/G]AAATAGGTGTCCTAA | 55666 |
rs771340226 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625798 | TGAAGGCAGAGATTT[G/T]GGGAAAAAAAAAACA | 55666 |
rs771345380 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601088 | GAAACCAACCACAGC[A/G]CATCACTTCCCAGAG | 55666 |
rs771388891 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583061 | ACGCAGAGTGTGTGT[A/G]ACACACCCATGTGCA | 55666 |
rs771408184 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633774 | CGATGGCGCGACCTC[A/G]GTTCACTGCAACCTT | 55666 |
rs771451644 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558345 | TCCCACCCAGGCCAT[C/T]GCAGGGCAGCCTCAG | 55666 |
rs771470813 | snp | C/T | 4.86962e-05 | 0.00493414 | synonymous-codon, intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81608778 | GTGGAAGGACATGTG[C/T]TTCACGGGAGGCTCG | 55666 |
rs771497015 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574205 | AATCTAATTAAGCTC[C/T]AATATGCAGAAACAT | 55666 |
rs771498243 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632848 | AAAATAGGATAACCC[G/T]GTCCTGCATTTTCCC | 55666 |
rs771502617 | in-del | -/CTTGA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591351 | GAGGCAGGAGAATCG[-/CTTGA]CCCCAGGTAGCAGAG | 55666 |
rs771506422 | snp | C/T | 6.68594e-05 | 0.00578146 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613303 | TAGGACCCTGGAATC[C/T]CATGGATCACTTACA | 55666 |
rs771566649 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581882 | GCAGAGGCGCAGGAA[G/T]AACTTAGACCTTCTG | 55666 |
rs771593724 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561895 | GAGACATCATGCCCA[A/G]CCTGCTTCATAGTTT | 55666 |
rs771616637 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591649 | TCACTGAGATGAACT[A/G]CAAACTCCCCTTTCC | 55666 |
rs771616978 | snp | G/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561399 | TACTGCGTCCCCCAT[G/T]GGTGCCTTTTCATGT | 55666 |
rs771638129 | snp | A/G | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637827 | TAATCCCAGCTACTC[A/G]GGAGTCTGAGGCCGG | 55666 |
rs771664056 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628229 | AAAAAAAAAGAAAAA[-/A]AAAAAGAAAAAGAAA | 55666 |
rs771705243 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617140 | GAGTCCTCAACCACC[C/T]AGTGGTCTTCACTGG | 55666 |
rs771726552 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615710 | CCCTGCCCAGAGGGG[A/G]CAGCTGAGTCCGAAA | 55666 |
rs771767341 | snp | C/G | 1.98643e-05 | 0.00315147 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572092 | CTTGTCTACGTCCTG[C/G]AATAGTCAGAGGGGA | 55666 |
rs771781603 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81566581 | AGGCACAGGGTGCCT[A/G]ATGTCAAATACCCGA | 55666 |
rs771792560 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581681 | GTATACTCCCGGGGC[A/G]CCAGCCAGCAAGGTG | 55666 |
rs771811467 | snp | C/T | 1.65685e-05 | 0.00287819 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629718 | TCAATACCCAGGCCA[C/T]AGATACCTTTTTCAA | 55666 |
rs771834639 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612297 | TGCTGCGGAACAGAG[A/G]TGGCCTCTGTGCTTC | 55666 |
rs771853366 | snp | C/T | 1.70551e-05 | 0.00292015 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569148 | CCATGATAAATGAGG[C/T]TGAAAATGGTGTGGC | 55666 |
rs771859788 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623236 | CAGCACTATGGGAGG[-/C]CAAAGCAGGTGGATC | 55666 |
rs771904510 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634290 | CAGGTGTGAGCCACC[-/A]ATGCCCAGCCCAGAA | 55666 |
rs771943262 | snp | A/G | 3.70021e-05 | 0.00430113 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604704 | GTGATTCTCAAACAT[A/G]ATATTGTCCACATGC | 55666 |
rs771954749 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585039 | GCCAGGCGTGGCAGC[A/G]TGCGCCTGTAGTCCT | 55666 |
rs771986718 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81577655 | TGAGTCCTGGCAACC[A/G]TCTGTCCTGCTCCAT | 55666 |
rs771990862 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604296 | CACAGCAGACGAGAT[A/G]AAAACACTGGATCAA | 55666 |
rs772037849 | in-del | -/AAGGG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575805 | TCCCACCTCCACCGC[-/AAGGG]AAGATGCAAAATTTT | 55666 |
rs772083175 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608393 | AGGCGCCTGCACAGT[C/T]GCTCTGCCTTGCTAG | 55666 |
rs772103829 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580508 | TCAGCTTCCAAGGGC[C/T]CCTCCCACCTCTACC | 55666 |
rs772151211 | snp | C/T | 1.65638e-05 | 0.00287778 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596200 | GCTTGTTCTGGAAGT[C/T]TCCTGCAGTGATGCA | 55666 |
rs772151825 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577245 | CCCACCCCATCACTG[C/T]GTAGTCCTCGCCAGA | 55666 |
rs772170490 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624111 | CCAACATGGTGAAAC[C/G]CCATCTCTCCTAAAA | 55666 |
rs772171132 | snp | A/G | 5.03943e-05 | 0.00501942 | synonymous-codon, intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81608757 | AGTCAGCTTCCGGAT[A/G]TAGGCGTGGAAGGAC | 55666 |
rs772213869 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570646 | CCCATCGTCTATCAG[A/C]CAGATGATGCCCCCA | 55666 |
rs772316947 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630026 | AGTACTGTCCTCTCA[A/G]CTCTTAGTTTCACTC | 55666 |
rs772350938 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628014 | TCAGGAGATGAAGAC[C/T]ATCCTGGCTAACATG | 55666 |
rs772462997 | snp | C/T | 9.02894e-05 | 0.00671837 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81565597 | GCCTCCAGCAGCAAG[C/T]TGATGCTGTCCTACA | 55666 |
rs772506061 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605474 | TCAATACAGTGAAAC[C/T]CTGTCTCTACTAAAA | 55666 |
rs772520186 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588695 | CTGTGTTGCAATGGT[C/T]GGATTTGGTGTTACT | 55666 |
rs772545323 | snp | C/G | 1.78541e-05 | 0.00298776 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567450 | ATTGGTGACCAGGAA[C/G]AGCAAGAGGTGGAAA | 55666 |
rs772555678 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622597 | GTTCTGTAGCCCAAG[C/G]TGGAGTACAGTGGCA | 55666 |
rs772574108 | snp | C/T | 0.000119031 | 0.00771371 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81600370 | GTTTGGCAGCAATTT[C/T]ATCGACCACTTCAGC | 55666 |
rs772605342 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601289 | AACCACAAAGAAGTT[C/T]ACGTTTGCTGGGTAT | 55666 |
rs772632945 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574565 | CAGCCGTCAAAGTGT[-/C]AGCAGCTTTATCTCC | 55666 |
rs772653691 | snp | A/G | | | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81564207 | CCTCAGCATCAGGCA[A/G]TATACCCAGGTGACA | 55666 |
rs772708979 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608388 | CAGCCAGGCGCCTGC[A/G]CAGTCGCTCTGCCTT | 55666 |
rs772723509 | snp | A/G | 1.66879e-05 | 0.00288855 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613308 | CCCTGGAATCTCATG[A/G]ATCACTTACAGCTGT | 55666 |
rs772812985 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585662 | GAAGACTCCATTTCT[-/G]GGGGGGGGGGGAAAG | 55666 |
rs772821930 | in-del | -/ACATACATATATATGTATATATACACAC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602900 | TATGTATATACACAT[-/ACATACATATATATGTATATATACACAC]ACATACATATATATG | 55666 |
rs772863925 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630628 | GGCTCACGTCTGTAA[A/T]TGTAGCACTTTGGGA | 55666 |
rs772907658 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564494 | AACAAAGAATTGTGT[C/G]AAAAGAAAACCTCGG | 55666 |
rs772957940 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558685 | CATCGGGTGAGAGGA[A/G]GAGGGCAGGCAGCAA | 55666 |
rs772958387 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619774 | ATCCCAGCTACTCAG[C/G]AGGCTGAGGCAGGAG | 55666 |
rs772968455 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580056 | TTCCAGGGCGCTATG[C/T]TCCTGCCCCTCCTCC | 55666 |
rs772975863 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81626273 | GTCAGCCAAGATCGC[A/G]CCACTGCACTCCAGC | 55666 |
rs772979318 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602708 | CTCCGTCTCAAAATT[A/T]AAAAAAAAAAAAAAA | 55666 |
rs772999332 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583946 | TTGCTTTCTAAGTTT[C/T]ACCCCTTATCTTTAA | 55666 |
rs773047856 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576266 | CACGGAAAGAGTATG[G/T]AGGTAGATGCATAGT | 55666 |
rs773064455 | snp | C/T | 3.20641e-05 | 0.00400388 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571971 | GTCCCACCTACAAGG[C/T]GCCCAATGGGTCCAC | 55666 |
rs773065024 | snp | A/G | 6.69591e-05 | 0.00578576 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622241 | CTATTGATGTAAACC[A/G]AGAAGCCATTATTTT | 55666 |
rs773073367 | snp | A/G | 1.85489e-05 | 0.00304534 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604705 | TGATTCTCAAACATG[A/G]TATTGTCCACATGCC | 55666 |
rs773099693 | snp | C/T | 2.3502e-05 | 0.0034279 | missense, nc-transcript-variant, synonymous-codon | NPLOC4 | GRCh38.p7 | 17:81559405 | GACCTGGGAGCTGCC[C/T]GCCAACTGTGCCTGC | 55666 |
rs773135884 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575135 | GAGGGAGTCTCGCTC[G/T]GTCGCCCAGGCTGGA | 55666 |
rs773137055 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81594551 | GAGGCCGAGGTGGGC[A/G]GATCACGAGGTCAGG | 55666 |
rs773152208 | snp | C/G | 1.65883e-05 | 0.00287991 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81569028 | CACCTGTGTCTCACC[C/G]AATACATCCCGGTTT | 55666 |
rs773153294 | snp | A/G | 1.65663e-05 | 0.002878 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629720 | AATACCCAGGCCACA[A/G]ATACCTTTTTCAAAA | 55666 |
rs773157990 | snp | C/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636789 | GCCACTACAGAGAAA[C/G]CCCTGGCGAGAGAAG | 55666 |
rs773189480 | snp | C/G | 1.65647e-05 | 0.00287786 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596202 | TTGTTCTGGAAGTCT[C/G]CTGCAGTGATGCACT | 55666 |
rs773207118 | snp | A/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578678 | TTATAAATCTAACAC[A/G]TCTTGTGAGAATGCA | 55666 |
rs773242319 | snp | A/C | 1.7086e-05 | 0.00292279 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604571 | GCTCATAAATCGCAG[A/C]CACTTCAGCCCTGAT | 55666 |
rs773244502 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600704 | GGAGCACTCAGGACT[A/G]AGGCAAGGCAAGGTC | 55666 |
rs773329716 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603167 | AGCAACAGAGTGAGA[C/T]GCTGTCTCAAAAAGA | 55666 |
rs773366241 | snp | A/G | 2.39083e-05 | 0.00345739 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559374 | GTGGAGCCCCCGACG[A/G]CGCCGTACTCATGGA | 55666 |
rs773386518 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591507 | TGGTCATTAACACGA[C/T]AGGTCATTCAAGAAA | 55666 |
rs773420457 | in-del | -/CTTC/CTTTTG | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615103 | GACGTCTGTTTCTTT[-/CTTC/CTTTTG]TTTTTTTTTTTTTTG | 55666 |
rs773449577 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612270 | AGAATTCTTACATGC[C/G]TATGAGCCCTGTGCT | 55666 |
rs773454121 | snp | A/G | 1.66676e-05 | 0.00288679 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596078 | AAAATATATTAACGA[A/G]GTGGTAATATTTACA | 55666 |
rs773473457 | in-del | -/GTGGCCTCT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612297 | TGCTGCGGAACAGAG[-/GTGGCCTCT]GTGCTTCCTAATAGG | 55666 |
rs773505341 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608834 | TGGCTGCCAAGACAC[-/A]AGAGTAAGCGAGTGC | 55666 |
rs773520835 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559161 | GTTCCTCCAGGGCTG[-/C]CCACTATGGGGCAGT | 55666 |
rs773552386 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566916 | TCGCCCTCTTCTCCC[C/G]CAACGGTGTCTCTTA | 55666 |
rs773594302 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624689 | CAAAGGTCGAAATAA[A/G]CACTACGACAGAAAA | 55666 |
rs773646103 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598973 | AAATCAAAATCAAAC[C/T]GAGAAAAATTAGGGC | 55666 |
rs773675656 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586057 | TGTGAGGCTGAGGTG[A/G]GTAGGTCACTTGAGA | 55666 |
rs773687797 | snp | A/G | 1.76714e-05 | 0.00297244 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567459 | CAGGAACAGCAAGAG[A/G]TGGAAATCTGAGATG | 55666 |
rs773707509 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632687 | TTACATTAAACATCC[G/T]CTTCAACCATTATGC | 55666 |
rs773746086 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589976 | CGGCAGATAGATCCC[C/T]AGGCTCACGGTAAGG | 55666 |
rs773759357 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586801 | GGCTCTCAGATGGCA[A/C]CCCTAAGGGGTTACA | 55666 |
rs773777582 | snp | C/G | 3.96723e-05 | 0.0044536 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565618 | CTGTCCTACAAGAAG[C/G]CAAAAGGAAGGTTCC | 55666 |
rs773777601 | snp | C/T | 7.87355e-05 | 0.00627388 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81600373 | TGGCAGCAATTTCAT[C/T]GACCACTTCAGCTTT | 55666 |
rs773784085 | in-del | -/G | 1.65721e-05 | 0.0028785 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597327 | CCAACCTTAAAAAAA[-/G]GAAAGTAGCTTTTAA | 55666 |
rs773838258 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565828 | CAAATAGGCCCAAGC[A/G]GGCATCTGTGCCTCT | 55666 |
rs773840070 | snp | A/G | 1.66599e-05 | 0.00288611 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569002 | AATTATGTTTCTAAA[A/G]ACAAAGAGCTCACCT | 55666 |
rs773917260 | snp | C/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560638 | CGTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAA | 55666 |
rs773917366 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572736 | AGGCAGAAGGGTCTG[C/T]GTTCCCCTCAGGTTG | 55666 |
rs773932791 | snp | C/T | 1.69648e-05 | 0.00291241 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569143 | CAAACCCATGATAAA[C/T]GAGGCTGAAAATGGT | 55666 |
rs773984619 | in-del | -/CAAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574865 | AAGACTGTCTCCAAA[-/CAAA]CAAACAAACAAACAC | 55666 |
rs774023855 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577228 | ACGGCGCTCTGACCC[A/G]CCCCACCCCATCACT | 55666 |
rs774089165 | in-del | -/CCCCT/CCCCTCCCCCT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617663 | AACACAAAAAATGCC[-/CCCCT/CCCCTCCCCCT]CCCCCTCCCCCTCCG | 55666 |
rs774102469 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624835 | GAGTAGGAGCAAGCA[C/T]AAAGACCAGGAGGCA | 55666 |
rs774115607 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591349 | CAGAGGCAGGAGAAT[C/T]GCTTGACCCCAGGTA | 55666 |
rs774166209 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632444 | CAGCCTCCTGAGTAT[C/G]TGGGATTACAAGTGC | 55666 |
rs774194987 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629957 | CCAGCTCAATCCTTC[C/T]AGAATATGATGCCGA | 55666 |
rs774227127 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602924 | ATATATGTATATATA[C/T]ACACACACATATATA | 55666 |
rs774318747 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616425 | ATAAGAACCAAAAAT[C/G]CAAATGTAGAAGAGT | 55666 |
rs774387683 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582277 | GCAAAGCTGAAGATG[C/T]CTGCACGTCACATCC | 55666 |
rs774395397 | snp | A/T | 3.31378e-05 | 0.00407036 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622151 | TTCCCTGCTTCCTCC[A/T]CAGAGGACACTTACT | 55666 |
rs774413778 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576272 | AAGAGTATGTAGGTA[G/T]ATGCATAGTTCTGGG | 55666 |
rs774439948 | snp | A/G | | | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564893 | AGGGCCGTAGCTCCC[A/G]GGCACTCTGGTGCTC | 55666 |
rs774478691 | in-del | -/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605362 | TACTTAAGAAAAAAA[-/C]CCAGTCAGGCACGGT | 55666 |
rs774480292 | snp | A/G | 1.65971e-05 | 0.00288067 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606730 | CGGCTGGCACTTAGT[A/G]CAGATGCCATTCGGC | 55666 |
rs774490472 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607569 | ACTGATCATTTTTGG[A/T]GGTGAGCCATTTTTG | 55666 |
rs774515254 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579915 | CCCCATTCTCCTCTG[C/T]GAGCTCACTCTCGGC | 55666 |
rs774529084 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568380 | CCCAAGTCCCCTGGG[C/T]GGATGGGCACTGAGG | 55666 |
rs774568689 | snp | G/T | 3.83318e-05 | 0.00437772 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636893 | TCCCGGCGTCCCCGC[G/T]CCCGCCCGGCCGCCG | 55666 |
rs774586516 | snp | C/T | 2.71595e-05 | 0.00368497 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606840 | GAGAAGCAACTTAAA[C/T]ATCACATTGGTGAAA | 55666 |
rs774599319 | snp | C/T | 3.56182e-05 | 0.00421994 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81565580 | CATTTCTGGTCCGCA[C/T]GGCCTCCAGCAGCAA | 55666 |
rs774689214 | snp | C/T | 3.71023e-05 | 0.00430695 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600301 | GATGCCCAACAGAGC[C/T]TGGCCACGCCCCCTG | 55666 |
rs774756860 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81620795 | CAGAGAGTGTGCACT[C/G]ACAGTCATTCTCTTT | 55666 |
rs774771660 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595133 | ACTCCCAGTCTCAAG[A/G]GATCCTCCTGGCTCA | 55666 |
rs774775100 | snp | C/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562598 | TAATCATCAGAGATG[C/T]AAATTAAAACCACAG | 55666 |
rs774802530 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572579 | GTAAAACCACCTTCC[A/C]CCATTTCTTGGAGCT | 55666 |
rs774851486 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601324 | CATATGGAGGTCATT[A/T]ATACCTCCAGAACGT | 55666 |
rs774855188 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625873 | AAAAATGAGGGTTGG[G/T]CGCGGAGGTTCAAGC | 55666 |
rs774889248 | snp | C/T | 0.000151297 | 0.00869631 | intron-variant, synonymous-codon | NPLOC4 | GRCh38.p7 | 17:81565377 | TACTCGTTGCATTGC[C/T]GATGGCACCTGCCAG | 55666 |
rs774893302 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588638 | CAGGCATGAGCCACC[A/T]TGCCAAGGACCCATC | 55666 |
rs774905196 | snp | A/G | 1.65715e-05 | 0.00287845 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613401 | CACCACGTTGGGAGC[A/G]CCAAAGACTTTGAAG | 55666 |
rs774917355 | snp | A/C | 1.68499e-05 | 0.00290253 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568981 | TAACAATCAGCAGTT[A/C]CCTTAAATTATGTTT | 55666 |
rs774943073 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624869 | AGGGTGTTGGAAACA[C/T]GGAGGCCAGAGGCCA | 55666 |
rs774946768 | in-del | -/TT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630070 | AATTCCTAATCACTA[-/TT]TATAGAGTATATGTA | 55666 |
rs774977743 | snp | A/G | 3.85431e-05 | 0.00438977 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81600384 | TCATCGACCACTTCA[A/G]CTTTTGGATCCTCAA | 55666 |
rs774997138 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592956 | CCATGGCACTCCAGC[A/C]TGGGTGACAGAACAA | 55666 |
rs775006972 | snp | C/T | 1.79968e-05 | 0.00299968 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567492 | ATCCAAGAACACAGA[C/T]GAGGTATTCTGAGAC | 55666 |
rs775131217 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589705 | GACTGTTAAACTTTT[-/G]GAAAAAAAGAAAAGA | 55666 |
rs775149333 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560189 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACTTGAA | 55666 |
rs775151504 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603413 | CCAACCTGGGCAATA[C/T]AGCGAGACCCTGACT | 55666 |
rs775220703 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616689 | AGCCAAGATGGTGCC[-/A]ACTGCCCTCCAGCCT | 55666 |
rs775327833 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613617 | TAAACAATGAGGTTT[C/G]TAACTTTTAAGATGA | 55666 |
rs775360765 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81577262 | TAGTCCTCGCCAGAC[G/T]GCCTGTCCGCACAGC | 55666 |
rs775365738 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557349 | CAGAATCAGACAAAT[C/T]GCCAATGCTTTTCCT | 55666 |
rs775371586 | snp | C/T | 3.31879e-05 | 0.00407343 | synonymous-codon, nc-transcript-variant, intron-variant | NPLOC4 | GRCh38.p7 | 17:81589004 | GGCGTAGCCAAGCTC[C/T]GGGGCGTCCTTGCAT | 55666 |
rs775373357 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591664 | GCAAACTCCCCTTTC[A/C]ACATGCAGCAGCAGG | 55666 |
rs775374294 | snp | C/T | 7.45657e-05 | 0.00610551 | missense, nc-transcript-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81559264 | GGCAGGCGCCCTAGG[C/T]CCTGGGGAGGCTGCA | 55666 |
rs775420152 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612198 | GGTATGCTGGTTTAC[A/G]AGGGCGCCGGCGGCC | 55666 |
rs775450846 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576375 | TCAACCAAACACAGA[C/T]TGAAAATACAGTATT | 55666 |
rs775476008 | snp | C/G | 1.66585e-05 | 0.00288599 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606822 | ACTTCCCCCTACATA[C/G]AAGAGAAGCAACTTA | 55666 |
rs775515513 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637057 | CCGCCACCGCCGCTC[C/T]AGCTTCGCCCGCCCG | 55666 |
rs775634033 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597669 | ATGCCTGTAATCCCA[C/G]CTACTCAGGAGGCTG | 55666 |
rs775646077 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597054 | GGAGGCATTGCTAGC[A/G]GTGAGCAGAGATTGC | 55666 |
rs775726399 | snp | A/G | 3.31268e-05 | 0.00406968 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81597257 | CACCTTATTTCGACT[A/G]TAGCGGACGGTACCC | 55666 |
rs775727134 | snp | C/G | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81629787 | GCTTCACTCCATCCG[C/G]GGACTGGACACGAAT | 55666 |
rs775729779 | snp | C/T | 1.90011e-05 | 0.00308224 | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636873 | CCGGCAAATCTGCTG[C/T]CTCATCCCGGCGTCC | 55666 |
rs775736528 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569684 | GGCAGGGGTGAATGT[A/G]AGGCCCTTGAGGAAC | 55666 |
rs775748101 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570829 | CAAGGACTCCCCATG[A/C]CTCACTTCCACAGGG | 55666 |
rs775769149 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604275 | AGTCAATGAGCAAAC[-/T]CTGGACACAGCAGAC | 55666 |
rs775793659 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603867 | TTGCAATAAAATGTA[C/T]GTAAAATACACTACA | 55666 |
rs775806336 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631066 | TAATCCCAGCTACCC[A/G]GGAGGCTGAGGCAGG | 55666 |
rs775815949 | snp | C/T | 1.68094e-05 | 0.00289904 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613288 | TAAGATCACCACAAG[C/T]AGGACCCTGGAATCT | 55666 |
rs775827344 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81621574 | CAGCACCCGTGTTCC[C/G]TAAAGGACCAGTCAA | 55666 |
rs775843971 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584219 | TCTTTGCTCCAACTG[A/G]TATTTTCCTGAAACA | 55666 |
rs775896475 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630092 | AGTATATGTAAAACA[C/T]TTTTTGTCTCTTCAG | 55666 |
rs775918748 | snp | A/G | 0.000150864 | 0.00868384 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565337 | ACCGGAGCCTGCCAC[A/G]TGCCTGGCAGGGAGG | 55666 |
rs775924239 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574699 | AGAAATCCAGGGATC[A/G]ATGTCTTTGTTAGCT | 55666 |
rs776014644 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588707 | GGTCGGATTTGGTGT[C/T]ACTGATCTCAAAGCC | 55666 |
rs776098226 | snp | A/G | 1.66073e-05 | 0.00288156 | missense, upstream-variant-2KB, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613420 | AAGACTTTGAAGCCC[A/G]GTGGAACTGACGTCT | 55666 |
rs776109703 | snp | A/G | 7.57432e-05 | 0.00615353 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610196 | CCCAGAACTTACTCC[A/G]CAGAGACTCTCACCT | 55666 |
rs776133677 | snp | A/G | 7.22804e-05 | 0.00601124 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600309 | ACAGAGCCTGGCCAC[A/G]CCCCCTGCTTGGCTG | 55666 |
rs776143912 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583182 | ATCAAAACTCGAAAA[A/C]CCTTCCTCCCCAGCA | 55666 |
rs776241378 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81573251 | TACATAAAAGTTTAC[A/G]TTTATTGGAGCTCTC | 55666 |
rs776288751 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616276 | CAGTGAGCTGAGATC[A/G]CACCACTGCACTCCA | 55666 |
rs776289742 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81634058 | TTTTTTTTTAGTAGA[C/T]GTGGGGTTTCACCGT | 55666 |
rs776298832 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591780 | GTCAGGAAATCCCTA[C/T]GTGGGAAGGATCACA | 55666 |
rs776371841 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574794 | CGAGGTGGGCAGACG[A/G]CTTGAGGTCGGGAGT | 55666 |
rs776384299 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601261 | ATCCTTGTAAATTAG[A/T]GAAAATCTGGCAAAC | 55666 |
rs776396946 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614485 | CAGCTTCTGCCATCA[C/T]CACCACCCCCCAAAA | 55666 |
rs776402120 | snp | A/G | 0.000153937 | 0.00877182 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572004 | GCCCAAGCTGTGCAT[A/G]GGGGGCACTTACGTC | 55666 |
rs776413086 | snp | A/G | 4.65712e-05 | 0.00482529 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559243 | GCCCGGTCCTAGCCA[A/G]CAGAGGGCAGGCGCC | 55666 |
rs776472450 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600300 | GGATGCCCAACAGAG[C/T]CTGGCCACGCCCCCT | 55666 |
rs776491205 | snp | A/G | 2.10113e-05 | 0.00324117 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604735 | CTGTACTTCTGTAGA[A/G]TTAACAAGAGTGGGC | 55666 |
rs776504123 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588371 | TCTCATCTCCACCCC[-/T]ATCCTTGAGACAGGG | 55666 |
rs776510975 | snp | A/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562210 | GCACTGCAGCCTGGG[A/T]GACAGGGTGAGATTC | 55666 |
rs776519914 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582685 | TGGGATTACAAGTGT[A/G]AGCCACCACACCTAG | 55666 |
rs776606677 | snp | A/G | 1.66073e-05 | 0.00288156 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606706 | CTGTCTGTTCAGCGT[A/G]ATGGCGCTCGGCTGG | 55666 |
rs776608255 | snp | C/T | 0.000151527 | 0.00870289 | intron-variant, utr-variant-3-prime | NPLOC4 | GRCh38.p7 | 17:81565309 | ACGGCCTGGACAACA[C/T]GTCTGCTCCATCACC | 55666 |
rs776647142 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623119 | GAATCACTTGAAGCT[C/G]GGAGGCAGAGGTTGC | 55666 |
rs776655960 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613785 | CACAGCCACAATGGA[C/T]CTGCTGGGTTTCAGG | 55666 |
rs776670219 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625226 | GAAACTATGTGGAGG[C/T]AACACCTGTGCAGGG | 55666 |
rs776675024 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599053 | CAGAACTTTGGGAGA[C/G]CAAGGCGGGTGGATC | 55666 |
rs776675440 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569514 | GGCCAGGAGGCCGCC[C/G]CAGGAGCTGACTTTG | 55666 |
rs776688893 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593140 | CTACTTACAATGATA[G/T]GAGATTAGAAGCAAT | 55666 |
rs776703632 | snp | C/T | 1.65614e-05 | 0.00287757 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81629776 | TGCTGTGATCCGCTT[C/T]ACTCCATCCGGGGAC | 55666 |
rs776707901 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598839 | CACCCCCAGCAGACA[C/T]GACTAGCCCACTGGG | 55666 |
rs776772541 | in-del | -/AAAAAAAAAA | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81568081 | GAGACTCTGTCTTCC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 55666 |
rs776793618 | snp | A/G | 6.63229e-05 | 0.00575822 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622281 | ACTCCTTTGCAACCT[A/G]AAACAAGGCCCAAAG | 55666 |
rs776852124 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81624216 | ACGAGGTCAGGAGAT[C/T]GAGGCCAGCCTGGCC | 55666 |
rs776868560 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560524 | CATCCTGGCTAACAT[-/A]GGTGAAACCCCGTCT | 55666 |
rs776906773 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585753 | GCACTGTGGGAGGCT[A/G]AGGCAGGCAGATTGC | 55666 |
rs776960006 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584816 | GGAATAACCTAACAA[A/G]TGATAGGTAAGACCT | 55666 |
rs776979766 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576616 | CAGAAAATATTTCAG[C/T]TTCTTTGTATAAAAG | 55666 |
rs777022536 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637133 | CCTCGGGCGCGAGGC[C/T]GGGAAACCAGGTTCC | 55666 |
rs777038409 | snp | A/C | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567835 | ACAGTAATTCCAGCA[A/C]TTTTTAGGAGGCCGA | 55666 |
rs777044991 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586407 | TTGAGTCCAGGAGTT[C/T]AAGACCGGCCTGGCC | 55666 |
rs777057979 | in-del | -/AAA | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635356 | AAAATAAAATAAGGT[-/AAA]TAAAAAAAAAAAAAA | 55666 |
rs777074208 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81556905 | CTTCAGGCGCTTTTA[C/T]TAGGTTCCACTGCAG | 55666 |
rs777085014 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585402 | GGTGTGGTGGTTCAC[A/G]CCTGTAATCCCAGCA | 55666 |
rs777138342 | snp | A/C | 1.70122e-05 | 0.00291647 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610177 | CCGCAGCCCCCCACA[A/C]TGGCCCAGAACTTAC | 55666 |
rs777150721 | snp | A/T | 1.65756e-05 | 0.00287881 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596126 | TATACCTGTAGCCAC[A/T]GCAGTAACAAACTTG | 55666 |
rs777158889 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81580660 | GGACTCGACCCACCA[C/G]GGCACTCCAAGCTTC | 55666 |
rs777210276 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630299 | TTGTTACTTTTTTTT[G/T]GCTTTTTTGAGACAG | 55666 |
rs777226558 | snp | C/T | 9.92802e-05 | 0.00704487 | missense, intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81608783 | AGGACATGTGCTTCA[C/T]GGGAGGCTCGAGATG | 55666 |
rs777258458 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603965 | AACCAGAAATACAAT[A/G]TGTAACTAGTTGGTG | 55666 |
rs777272596 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565678 | CTGCTAGAACAGGTT[C/T]CTTTCTCCCCAACAT | 55666 |
rs777272602 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81630683 | CTCAGAAGTTCAAGA[C/T]CAGTGGGCAACATGG | 55666 |
rs777277805 | snp | A/C/G | 0.000206277 | 0.0101539 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606825 | TCCCCCTACATAGAA[A/C/G]AGAAGCAACTTAAAC | 55666 |
rs777277850 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576093 | GACGATGACCAGAAG[A/T]AAGACATGAGGAGAC | 55666 |
rs777345020 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571070 | CACCCTAGGTAGTCT[A/G]AAAACCAGATGCCTT | 55666 |
rs777348466 | snp | A/G | 1.66763e-05 | 0.00288753 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606682 | CTAGACAGACAGGGA[A/G]CATCTCACCTGTCTG | 55666 |
rs777369778 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81584883 | AAAGAACATGGGAAC[C/G]AGGCCCAGCACGGTG | 55666 |
rs777377303 | in-del | -/ACTT | 1.65652e-05 | 0.0028779 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622160 | TCCTCCTCAGAGGAC[-/ACTT]ACTTGATTTTTAGCA | 55666 |
rs777380236 | in-del | -/AAAAAAAAA | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614275 | GGGAGGCTCCATCTC[-/AAAAAAAAA]AAAAAAAAAAAAAAA | 55666 |
rs777431842 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81560047 | GCCTCCAGTTTTGAG[C/G]TAATATGAACAAAGT | 55666 |
rs777433049 | snp | A/G | 1.65704e-05 | 0.00287836 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629836 | CATGATGGTTACTGC[A/G]CAGCCTAGTGAGGTC | 55666 |
rs777445953 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623136 | GAGGCAGAGGTTGCA[A/G]GGAGCCGAGATCGTG | 55666 |
rs777448979 | snp | A/G | 1.68258e-05 | 0.00290045 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606763 | CGGGAGGTGCCCCTC[A/G]CACCCTGACTTAATC | 55666 |
rs777455925 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616935 | GGCGGGATTCTAGGA[C/T]ATGGAAGTGGCAGGC | 55666 |
rs777459214 | snp | A/C | 1.73646e-05 | 0.00294652 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588933 | AGTTCTTTTTCTTAC[A/C]ATACTTTTACCTTAT | 55666 |
rs777472951 | snp | C/T | 0.000548246 | 0.0165476 | intron-variant, missense | NPLOC4 | GRCh38.p7 | 17:81565472 | CTCCGGCCCCAGCCA[C/T]GGGGTGCCGGGGCAG | 55666 |
rs777516098 | in-del | -/TA | 3.3568e-05 | 0.00409669 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568990 | GCAGTTACCTTAAAT[-/TA]TGTTTCTAAAGACAA | 55666 |
rs777538891 | snp | C/T | 3.89962e-05 | 0.0044155 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636975 | CCCGGGCCGCCGCCG[C/T]CTGCCGCCCCAAGGG | 55666 |
rs777542326 | snp | C/G | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81566793 | ATTTCCTGTTGGCTT[C/G]AACAGTGAAGAAAAA | 55666 |
rs777545519 | snp | A/C | 1.99774e-05 | 0.00316043 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572096 | TCTACGTCCTGCAAT[A/C]GTCAGAGGGGAACAG | 55666 |
rs777629458 | in-del | -/TTTTTTT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587327 | TTTTTTTATTTTTTA[-/TTTTTTT]GAGACGGAGTCTTGC | 55666 |
rs777648990 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81568695 | GAAGGGCAGCAGGTG[A/T]CCAGGCAGGGGCCAG | 55666 |
rs777713937 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633724 | CTTTTCTCCCCCCAA[C/G]ACAGAGTCTTGCTCT | 55666 |
rs777827629 | in-del | -/CTAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587479 | TGCCACCATGCCCGG[-/CTAA]CTTTTTGTAGTTTTA | 55666 |
rs777898444 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81564270 | GTTAAAATTATTTTT[-/A]AAAAAACAAACAAAT | 55666 |
rs777921340 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81609298 | GTTAGCTTTACAGGC[G/T]TGAGCCACTGAGTCT | 55666 |
rs777923471 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596499 | TGAACCCAGGAGGAG[A/G]AAGCTGTAGTGAGCC | 55666 |
rs777955178 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579713 | CTCCTTTGCTGGACA[C/T]CAGGAAGCAGTACAT | 55666 |
rs778025770 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582404 | GTTCTGTGTGTGTAT[G/T]TATGTCTGCATGTTT | 55666 |
rs778026200 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574106 | TCAAACTAAATCACC[A/G]TTTCCAAAAATACAG | 55666 |
rs778075505 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625683 | CTACAATGAGATATG[A/G]TCACACCACTGCACT | 55666 |
rs778098233 | snp | C/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81562320 | GAGGTGGGTGGATCA[C/G]TTGAGGTCAGGAGTT | 55666 |
rs778109628 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81614047 | TTTGGGAGGCTGAGG[C/T]AGATGGATCACAAGG | 55666 |
rs778123012 | in-del | -/TTTC | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615097 | CATCAGAGACGTCTG[-/TTTC]TTTCTTTTTTTTTTT | 55666 |
rs778123485 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590413 | TGGGGGCAGCCTGAG[C/T]CTTTGGAGGAGGCAG | 55666 |
rs778138519 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583035 | GCCAGCACAGCAGCC[A/T]CTGCCACGTGACGCA | 55666 |
rs778145634 | snp | C/T | 1.68151e-05 | 0.00289953 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604620 | GTGCTCCGTGTACCG[C/T]CCGTATAAGTACCCA | 55666 |
rs778188030 | snp | C/T | | | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564004 | GGGAATTGCTTCAAC[C/T]CAGGAGGCAGAGTTT | 55666 |
rs778199159 | snp | G/T | 3.31274e-05 | 0.00406972 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622233 | TCTTGTTTCTATTGA[G/T]GTAAACCGAGAAGCC | 55666 |
rs778219768 | snp | C/T | 5.86986e-05 | 0.00541718 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81572085 | TGCCAAACTTGTCTA[C/T]GTCCTGCAATAGTCA | 55666 |
rs778233631 | snp | C/T | 1.88304e-05 | 0.00306837 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604535 | TCAGGAACTTGAATC[C/T]CGTCATGTTTACCTG | 55666 |
rs778287536 | snp | C/T | 1.6585e-05 | 0.00287962 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567563 | ATAAACATGAATGTT[C/T]CATACAGTTCCCCAG | 55666 |
rs778290313 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625826 | ACAGCCTTAGGAACC[C/T]ATGGTACAGGATCAA | 55666 |
rs778310694 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81565791 | CGCAAGTGCTAAATT[-/G]AACTAGAATTTAAAT | 55666 |
rs778310840 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628211 | CGAGACTCCCTCTCA[-/T]TAAAAAAAAAAAGAA | 55666 |
rs778383903 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558827 | AGCAGTCAGACAAGG[A/G]GGTAACCAAGAGCTC | 55666 |
rs778399557 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616160 | GTCTCTGCTAAAAAT[-/A]AAAAAAAAAAATTAG | 55666 |
rs778403867 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81592427 | CATGGCAAGTCTGAG[C/T]ACCAAGAGGGGTGAT | 55666 |
rs778487947 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557924 | ATGTTCTCTGTTCAT[A/G]GTGCCAAGAATGTGG | 55666 |
rs778598953 | snp | A/G | 6.71434e-05 | 0.00579372 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606659 | GTTTCTCAGCCATGA[A/G]AACAAATCTAGACAG | 55666 |
rs778599497 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602401 | AAAAAAATTAAACAA[-/T]TAAACAATTAAAAAA | 55666 |
rs778623935 | snp | C/T | 0.000135254 | 0.00822245 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563931 | CGTACATAAAGATGG[C/T]AACGCCAGGTGTGGT | 55666 |
rs778664367 | snp | C/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81639023 | AAGCTAAACTATAAA[C/T]TAAGCGCCTCCCGAA | 55666 |
rs778675128 | snp | C/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81560913 | CCACACTGATGAATG[C/T]GTAACGGCTTCTCAT | 55666 |
rs778680478 | snp | C/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81566547 | CCTGGGCTGACTAGG[C/G]AAGGCACAGGCAGGG | 55666 |
rs778686825 | snp | C/T | 1.65677e-05 | 0.00287812 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629826 | GCAAACAAAACATGA[C/T]GGTTACTGCACAGCC | 55666 |
rs778691243 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81600058 | GTCCTCATGAAGTGT[G/T]GCTGGAAGGCTGAAA | 55666 |
rs778711944 | snp | A/G | 1.65781e-05 | 0.00287902 | | | GRCh38.p7 | 17:81597213 | TGTAACCAAGCCATA[A/G]GGCCACACGCACAGT | 55666 |
rs778776677 | snp | G/T | 1.65754e-05 | 0.00287879 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629702 | AAAAATATCCTGAGG[G/T]TCAATACCCAGGCCA | 55666 |
rs778779506 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571566 | ACACTGTGGGCTGTG[A/G]CAGCTGTGCTGGGGC | 55666 |
rs778785789 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598604 | GAGGGTATGAGGATC[C/T]GAAACCTGTGACCCA | 55666 |
rs778799862 | snp | C/T | 1.65638e-05 | 0.00287778 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596176 | GAGAGAGCCGGCACA[C/T]GTTGGGATGCTTGTT | 55666 |
rs778875082 | in-del | -/AA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623471 | TTTGTTTCAAAAAAA[-/AA]AAAAAAAAAAAAAGC | 55666 |
rs778951561 | snp | C/T | | | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81565272 | GGTTTATAAAATTTA[C/T]AGGGCTGTGTACCTA | 55666 |
rs778968409 | snp | A/G | 1.71702e-05 | 0.00292998 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81610164 | GACAGCTGTCTACCC[A/G]CAGCCCCCCACACTG | 55666 |
rs778971304 | snp | C/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636194 | CAGGATGGTCTCGAA[C/G]TCCTGACCCCAGGTG | 55666 |
rs778973591 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81570548 | TTGGAGGGGAACAGA[A/G]CCAAAGTCCACACAG | 55666 |
rs778988952 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590689 | AAAAAACCCTCAATA[C/T]CTCTATTTCAGTTTC | 55666 |
rs779182626 | snp | C/T | 2.0013e-05 | 0.00316324 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604511 | CCCACAGCCTCCAAA[C/T]ACAGAAACTCAGGAA | 55666 |
rs779272016 | snp | A/G | 3.8523e-05 | 0.00438862 | missense, nc-transcript-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567425 | CACGCACCTGCAGAG[A/G]CATAACTTCATTGGT | 55666 |
rs779280652 | snp | C/T | 1.65633e-05 | 0.00287774 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622223 | ATCTCTCCGGTCTTG[C/T]TTCTATTGATGTAAA | 55666 |
rs779282690 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81583753 | GCTGCATATGGGACA[G/T]GGCAAAGCTGTAGAC | 55666 |
rs779339591 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629013 | CCTCACCAGCAGCTG[A/G]GACTACAGGTGCCCG | 55666 |
rs779357719 | snp | A/C | 2.03077e-05 | 0.00318644 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81600364 | GGCCAAGTTTGGCAG[A/C]AATTTCATCGACCAC | 55666 |
rs779370775 | snp | C/T | 1.66054e-05 | 0.00288139 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622123 | CAGATCATGGGGACC[C/T]CATTTCCCCCCATTC | 55666 |
rs779422951 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558861 | GCCAGAAAAACATGG[A/G]GGCAGGGAGGCCAAA | 55666 |
rs779536834 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81563224 | GGATTACAGGCGCTC[A/G]CCACCATGCCCAGCT | 55666 |
rs779543651 | in-del | -/AACT | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558465 | TTTACTTCAAGGGAG[-/AACT]GACTGGTGCCCCCGT | 55666 |
rs779560261 | snp | A/G | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81566540 | GCAGTTCCCTGGGCT[A/G]ACTAGGGAAGGCACA | 55666 |
rs779622132 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615918 | CAGAACCAGGGATGA[C/T]GCCATTTGGTTCAGA | 55666 |
rs779628299 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81601119 | TGGACCAAGCTTACC[A/G]AAATCATTAATGTTC | 55666 |
rs779642467 | snp | C/T | 1.82817e-05 | 0.00302333 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604541 | ACTTGAATCCCGTCA[C/T]GTTTACCTGAGGTGG | 55666 |
rs779644376 | snp | A/G | 5.01945e-05 | 0.00500946 | synonymous-codon, nc-transcript-variant, missense | NPLOC4 | GRCh38.p7 | 17:81559364 | GGCCGTGTGTGTGGA[A/G]CCCCCGACGGCGCCG | 55666 |
rs779718754 | snp | A/G | 4.97541e-05 | 0.00498744 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629683 | GCAGTAAGAGTAGAG[A/G]ATGAAAAATATCCTG | 55666 |
rs779739880 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81599818 | AACTAGGAAGAATTG[G/T]AGGCTCAGAGAGCTA | 55666 |
rs779743562 | snp | C/T | 2.27762e-05 | 0.00337455 | synonymous-codon, nc-transcript-variant, missense | NPLOC4 | GRCh38.p7 | 17:81559394 | GTACTCATGGAGACC[C/T]GGGAGCTGCCCGCCA | 55666 |
rs779787992 | snp | A/G | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636384 | CCGGCAAGTTACTGT[A/G]TTTTCATTTTCCCAG | 55666 |
rs779810644 | snp | G/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567894 | CAGTCTGGCCAACAT[G/T]GCGAAACCCCGTCTC | 55666 |
rs779811320 | snp | G/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561697 | TGGGATCCTCCCATT[G/T]CAGCCTCCCCAGAAG | 55666 |
rs779826923 | snp | A/T | 0.000248429 | 0.0111424 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81622235 | TTGTTTCTATTGATG[A/T]AAACCGAGAAGCCAT | 55666 |
rs779858943 | snp | A/G | 0.000230053 | 0.0107226 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608860 | AGTGCAGTCTCACAC[A/G]TGCCGGTCACTCCAG | 55666 |
rs779900595 | snp | A/C | 3.32613e-05 | 0.00407793 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81569088 | AAAAGTGTAAACTGG[A/C]TCCTTGGGGAAAGTT | 55666 |
rs779930700 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602876 | GAGATCTGTCTCCAC[A/C]CACACTATATATGTA | 55666 |
rs779948804 | snp | A/T | 1.67069e-05 | 0.00289019 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608711 | TACGCACAACCAGGT[A/T]ACAGCAAGTTGCTTA | 55666 |
rs779990567 | in-del | -/AT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602966 | TATATATACACACAT[-/AT]ATATATACACAAATA | 55666 |
rs780115153 | snp | A/G | 4.49832e-05 | 0.00474232 | synonymous-codon, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81600349 | TCAGTACCTTCCGCA[A/G]GCCAAGTTTGGCAGC | 55666 |
rs780127963 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578306 | GCTTCCTCTCACACA[C/T]TCTAGTCTCAGCACT | 55666 |
rs780197945 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81571621 | GACAGCTGACAGCCA[C/T]ACACCAAGCACAGCA | 55666 |
rs780199960 | snp | C/G | 3.00422e-05 | 0.00387559 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81613542 | CCCTTACCACCTGAG[C/G]TTCATGGAAGCCCAA | 55666 |
rs780221859 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612716 | ATTTAAAAGGAATTG[C/T]AAAAAATCTAAAATA | 55666 |
rs780292112 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576859 | CCAGAGTCACGGGCG[C/T]GAGGGCAAGGCTGGT | 55666 |
rs780292351 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598742 | CAGCAGTTGAGTCCC[A/G]GCAATTGTCACTTCT | 55666 |
rs780311943 | snp | A/G | 8.49365e-05 | 0.00651621 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567413 | ACCACACTTGGACAC[A/G]CACCTGCAGAGGCAT | 55666 |
rs780313601 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612200 | TATGCTGGTTTACGA[C/G]GGCGCCGGCGGCCGT | 55666 |
rs780375846 | snp | C/G | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637527 | TTTCAGGCCGGGCGC[C/G]GTGGCTCATACCTGT | 55666 |
rs780380508 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81593167 | AATTCTGTTTTATAA[-/T]ATAGCCACAAAACAG | 55666 |
rs780388358 | snp | G/T | 1.66258e-05 | 0.00288316 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597364 | CCTCAAGATAGACGA[G/T]GAATGGCTGGGCGCA | 55666 |
rs780397706 | snp | C/T | 1.75203e-05 | 0.00295971 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81565556 | TCTTCCATGTCTGGG[C/T]GAGCTCCTCATTTCT | 55666 |
rs780474504 | snp | C/T | 3.31312e-05 | 0.00406995 | missense, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81613391 | TCTCATCCTCCACCA[C/T]GTTGGGAGCGCCAAA | 55666 |
rs780482780 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616854 | ATATCAACCTCTACA[C/T]GGGATATTAAATGAA | 55666 |
rs780499431 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576029 | GGCTATAGCAAACAG[A/G]GCAGTTTGGTAACAA | 55666 |
rs780505200 | snp | A/G | 5.3968e-05 | 0.00519433 | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81559226 | AGGAAGGGCTGGGCT[A/G]GGCCCGGTCCTAGCC | 55666 |
rs780589329 | snp | A/C | | | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81565539 | GGCCCACTGCTCAGA[A/C]CTCTTCCATGTCTGG | 55666 |
rs780596917 | snp | C/T | 1.75693e-05 | 0.00296384 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588922 | TCCATGTACAGAGTT[C/T]TTTTTCTTACCATAC | 55666 |
rs780649909 | snp | C/T | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81636325 | TTTACAACATTCCTT[C/T]TAAAGAGGAATTGTC | 55666 |
rs780654350 | snp | C/G | | | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81596167 | GTCCGTCTGGAGAGA[C/G]CCGGCACATGTTGGG | 55666 |
rs780686012 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81590817 | AAAAAGGTGAGGGAG[A/G]AGATAGAGCTGGCCG | 55666 |
rs780693602 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81575446 | AAAATAGTCCAGTCC[A/G]TGTGCAACGACTGGA | 55666 |
rs780707699 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81607101 | TCACTAACATCCGAG[-/A]AAGCTTTCAAGAATA | 55666 |
rs780753896 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81629369 | ACTAATTTTTGTATT[C/T]TTAGTAGACGGGGTT | 55666 |
rs780756395 | snp | C/T | 1.66065e-05 | 0.00288149 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81622129 | ATGGGGACCTCATTT[C/T]CCCCCATTCCCTGCT | 55666 |
rs780775919 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603802 | TCTCCCTAAATAGTA[C/T]AGCATGCATATCATT | 55666 |
rs780790774 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81579578 | AAACCTGCATCCCAT[C/T]GCTCCTGCCAGCTCC | 55666 |
rs780855954 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569207 | CAGAGCCCAAATTAA[C/T]GACTCCTAGCAATTC | 55666 |
rs780869307 | in-del | -/GAG | | | cds-indel, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81557623 | CTCATCTCAGGACCA[-/GAG]GAGACAGCAGAGGAC | 55666 |
rs780876762 | snp | C/T | 1.81132e-05 | 0.00300936 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81606814 | GGCAACAAACTTCCC[C/T]CTACATAGAAGAGAA | 55666 |
rs780878214 | in-del | -/AAAAAGAAAC/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616333 | TCAAAAAAAAAAAAA[-/AAAAAGAAAC/C]AAAAAGAAAAGCAAA | 55666 |
rs780887444 | snp | C/T | 3.77209e-05 | 0.0043427 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81589132 | GACCTTTAAAAAGAG[C/T]CTACCAAACGGCATT | 55666 |
rs780892360 | snp | C/T | 2.68871e-05 | 0.00366645 | missense, nc-transcript-variant, synonymous-codon | NPLOC4 | GRCh38.p7 | 17:81559339 | GCTGACAGGCCCACA[C/T]GGCTGCAGTGGCCGT | 55666 |
rs780950817 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81619331 | GCAGTGAGCTGAAAT[C/T]GCGCCACTGGACTCT | 55666 |
rs780955661 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81596438 | CACACCAAAACCTGG[C/T]CTCTACTAAAAATAA | 55666 |
rs780979076 | snp | C/T | 7.72171e-05 | 0.0062131 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81608698 | ACAAAAAGGAATTTA[C/T]GCACAACCAGGTTAC | 55666 |
rs780994118 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588139 | AGAAGTCCAGATCAA[C/T]GAATGTGAAGACTAA | 55666 |
rs781071299 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578464 | AACAGATAAACGGTA[C/T]GACTGGTCCGTTTTC | 55666 |
rs781073969 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612737 | ATCTAAAATAAACAA[C/T]GTACATATGCATAAG | 55666 |
rs781081833 | snp | C/T | 0.000185925 | 0.00963993 | missense, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637400 | CCAAACTTCTCTCCA[C/T]GCACAGGTAAGTAGA | 55666 |
rs781132006 | in-del | -/AAAAAAAAAG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81628215 | GACTCCCTCTCATAA[-/AAAAAAAAAG]AAAAAAAAAAGAAAA | 55666 |
rs781136580 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81606957 | GGAAGATGGGCTAAG[A/G]ATGATTCTAATGGAA | 55666 |
rs781148508 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612839 | GCAGGGATGGAGAGC[A/G]CACACTAGTGTGGCA | 55666 |
rs781159556 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81558928 | GGCAGCATCGGCCCC[-/T]CCCTGTGCGCCCCAA | 55666 |
rs781258985 | snp | A/G | 2.64806e-05 | 0.00363863 | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81567377 | TCTCTTTGCAGCCAA[A/G]GCCCACTTGCTCAAG | 55666 |
rs781263763 | snp | C/T | 3.54849e-05 | 0.00421203 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81565531 | TCGATGGTGGCCCAC[C/T]GCTCAGACCTCTTCC | 55666 |
rs781312933 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81588108 | TGGATGAGATTAACT[A/G]CAGATGAGACACTGT | 55666 |
rs781319171 | snp | A/T | | | intron-variant, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81561354 | TTTTAAGTTTCAGAT[A/T]GAAGTCATGTTGTGT | 55666 |
rs781367836 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586777 | GTCACCTCACAAAGA[A/G]CTCTACCAGGCTCTC | 55666 |
rs781384105 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81598094 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55666 |
rs781420432 | in-del | -/AG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633727 | TTCTCCCCCCAAGAC[-/AG]AGTCTTGCTCTGTCA | 55666 |
rs781431386 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81591111 | AGCGCCGGGGAGCCA[C/T]GGTGCAGACATCTGG | 55666 |
rs781440103 | snp | A/G | 1.66032e-05 | 0.0028812 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81597356 | AAACATCTCCTCAAG[A/G]TAGACGATGAATGGC | 55666 |
rs781458708 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81582946 | ACACAAAAACCCAAG[A/G]AGCCTCCCGGCCAGG | 55666 |
rs781523149 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633526 | ATAATTTGTACGATG[G/T]AAAGTTCTGGCCTAG | 55666 |
rs781525701 | snp | A/G | 1.68616e-05 | 0.00290353 | intron-variant | NPLOC4 | GRCh38.p7 | 17:81569129 | AATGAAGAAAAACAC[A/G]AACCCATGATAAATG | 55666 |
rs781526127 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81572641 | GCTCTCGGGCACTGG[C/G]ACTCCCCACTGGGAG | 55666 |
rs781611590 | snp | C/T | 1.75993e-05 | 0.00296637 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81604675 | CAGAAGTCAAGAAAG[C/T]GGTCAGCGACGGTGT | 55666 |
rs781613099 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632078 | CCTCCCAGGTTCAGG[C/T]GATTCTCCTGTCTCA | 55666 |
rs781619418 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81613278 | ATTCACCCATTAAGA[C/T]CACCACAAGTAGGAC | 55666 |
rs781629817 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81566319 | TCTGGGCAACAGAGC[A/G]AGACTCCGTCTTAAA | 55666 |
rs781641282 | snp | A/G | 1.90663e-05 | 0.00308752 | missense, nc-transcript-variant | NPLOC4 | GRCh38.p7 | 17:81572060 | GGCCGGGCCAGCTGG[A/G]TGATCTCGTTGCCAA | 55666 |
rs781645892 | in-del | -/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81586061 | AGGCTGAGGTGGGTA[-/G]GTCACTTGAGATCAG | 55666 |
rs781698367 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81612221 | CGGCGGCCGTCCCTC[C/T]GGGGCTCAGTCAGAC | 55666 |
rs781776183 | snp | C/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81638606 | GCCCGGCTGGGGATC[C/T]GCGGTTTTAAGGATA | 55666 |
rs796076511 | in-del | -/AA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574901 | CACACACACACACAC[-/AA]ACACAAAAGCATGTG | 55666 |
rs796112541 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576654 | ACGAAAACCTGGCGT[G/T]TGTTTGCAACACACG | 55666 |
rs796124251 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574667 | GGAAGCAGTGGCGCC[A/C]AGGTCTTGACACCAA | 55666 |
rs796216698 | snp | A/G | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637883 | AGGTTAGAATGAACT[A/G]AGTTGGTGCCACTGC | 55666 |
rs796235675 | in-del | -/AT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81605819 | GCAAAAAACAAACAC[-/AT]TTTCTTTTTTTTTTT | 55666 |
rs796238813 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631445 | ATATATATTTTTTTT[A/T]TTTTTTTTTTTTTTT | 55666 |
rs796265809 | in-del | CC/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631465 | TTTTTTTTTTTTCCC[CC/T]ACGGCAAGCCTAAAA | 55666 |
rs796267673 | snp | C/T | | | downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81556647 | GGCACCCAAGGGCGG[C/T]GGGGCCGTCAAACAC | 55666 |
rs796279220 | in-del | -/CA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574900 | ACACACACACACACA[-/CA]AACACAAAAGCATGT | 55666 |
rs796294509 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631448 | TATATTTTTTTTTTT[A/T]TTTTTTTTTTTTTTC | 55666 |
rs796299909 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637462 | TCATGTTTTTTTTTT[-/T]AAGTATTTTTTAAAT | 55666 |
rs796300782 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81604868 | GATGGTGCATGCCTG[C/T]GGTCCCAGATACTCA | 55666 |
rs796314057 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633349 | AATGTTCCTTCAAAC[A/G]ATGACTCTGGAACAA | 55666 |
rs796370065 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631449 | ATATTTTTTTTTTTT[A/T]TTTTTTTTTTTTTCC | 55666 |
rs796410055 | multinucleotide-polymorphism | AAA/GTC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81581373 | AAAAAAAAAAAAAAA[AAA/GTC]GTTAATAAAATCACC | 55666 |
rs796411845 | in-del | -/AAA | | | upstream-variant-2KB, intron-variant | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81635358 | AAATAAAATAAGGTT[-/AAA]AAAAAAAAAAAAAAA | 55666 |
rs796434402 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81595265 | AAGGCAAAACCCAGT[C/T]GCTACTAAAAATACA | 55666 |
rs796443262 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631446 | TATATATTTTTTTTT[A/T]TTTTTTTTTTTTTTT | 55666 |
rs796483890 | in-del | -/AC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81602923 | TATATATGTATATAT[-/AC]ACACACACATATATA | 55666 |
rs796498366 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603964 | AAACCAGAAATACAA[C/T]GTGTAACTAGTTGGT | 55666 |
rs796509802 | in-del | -/AC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81625517 | TTCTAGAACTGAAAA[-/AC]ACAAGAACAGAAATA | 55666 |
rs796515159 | snp | C/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618546 | AGGTGAGGGGTCAGT[C/G]CCCCCGCCCGGCCAG | 55666 |
rs796536164 | in-del | AGC/CAAAAAGAAAAGA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616343 | AAAAAAAAAAGAAAA[AGC/CAAAAAGAAAAGA]AAGCTGCTAAATCTG | 55666 |
rs796590203 | multinucleotide-polymorphism | CAC/TAT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81603012 | CACACACACACACAC[CAC/TAT]TATAAAAGTCAGACA | 55666 |
rs796630477 | in-del | -/TTTTT | | | intron-variant, upstream-variant-2KB | TSPAN10, NPLOC4 | GRCh38.p7 | 17:81637458 | ACCTTCATGTTTTTT[-/TTTTT]AAGTATTTTTTAAAT | 55666 |
rs796635875 | in-del | -/AC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623808 | GTCTCAAAAAAAAAA[-/AC]AAAACTCAATTCCAA | 55666 |
rs796639761 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81631447 | ATATATTTTTTTTTT[A/T]TTTTTTTTTTTTTTT | 55666 |
rs796648278 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81618556 | TCAGTGCCCCCGCCC[A/G]GCCAGCCGCCCCGTC | 55666 |
rs796670630 | in-del | -/AC | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81574879 | AACAAACAAACAAAC[-/AC]ACACACACACACACA | 55666 |
rs796671401 | snp | A/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81578647 | GAGAAGTGCCGAGCA[A/T]AGGGGGAAGAGCCCC | 55666 |
rs796705223 | snp | C/T | | | intron-variant, upstream-variant-2KB | NPLOC4 | GRCh38.p7 | 17:81615104 | GACGTCTGTTTCTTT[C/T]TTTTTTTTTTTTTGA | 55666 |
rs796741069 | in-del | -/A | | | intron-variant, downstream-variant-500B | NPLOC4 | GRCh38.p7 | 17:81564789 | GCCAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55666 |
rs796780555 | in-del | -/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632340 | TTTCTTTTTTTTTTT[-/T]CAGCTCTTGTTGCCC | 55666 |
rs796813821 | snp | A/C | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587660 | AAAGGAAAAAAGAAA[A/C]AAAGAAAAAAGTTGT | 55666 |
rs796829635 | snp | G/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81587679 | GAAAAAAGTTGTTTT[G/T]TTTTTTTTTTTTGAG | 55666 |
rs796839741 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81615641 | CAGTAATTCACTCAC[-/A]AGCTTTGGGCCTACA | 55666 |
rs796854656 | snp | A/G | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81616329 | CTGTCTCAAAAAAAA[A/G]AAAAAAAAAGAAAAG | 55666 |
rs796909325 | snp | A/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81627310 | GGCAGGGAAATGGCA[A/T]GAACCTGGGAGGCAG | 55666 |
rs796931893 | in-del | AA/GGG | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81585674 | CTGGGGGGGGGGGGA[AA/GGG]GAAAGAAATCAGAGG | 55666 |
rs796932763 | in-del | -/GCGT | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81576650 | AAGAACGAAAACCTG[-/GCGT]GTGTTTGCAACACAC | 55666 |
rs796978290 | snp | C/T | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81632061 | ACTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAG | 55666 |
rs796986221 | in-del | -/A | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81617255 | GACAGATTTAGGGGG[-/A]AAAAAAATCAGATTA | 55666 |
rs797014502 | in-del | -/GA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81633333 | TGAAGGGGAACATGT[-/GA]ATGTTCCTTCAAACG | 55666 |
rs797016686 | in-del | -/AAAAAAAAA | | | intron-variant | NPLOC4 | GRCh38.p7 | 17:81623465 | GCAAGACTTTGTTTC[-/AAAAAAAAA]AAAAAAAAAAAGCAA | 55666 |