SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs191758778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20370523 | TTATTCCATTCATCA[A/G]CATGCAGTATCACAT | 7011 |
rs191782919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396774 | AAACAAATGAGAAGG[C/T]CAGGCACAGTGGCAT | 7011 |
rs191784339 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365466 | TTTTAGTAGAGACGG[G/T]GTTTCACCATATTGG | 7011 |
rs191984652 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20400785 | ACATCTGGTATAATG[A/T]TCTATGATGCCAACA | 7011 |
rs192006797 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TEP1 | GRCh38.p7 | 14:20397549 | ACCATTTATAATGAC[A/G]AATGTATGTAAATCC | 7011 |
rs192013641 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372163 | CCCTTACTCCCACCA[A/G]GAATCCAAGGAGCTG | 7011 |
rs192046174 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TEP1 | GRCh38.p7 | 14:20390378 | ACACAGCAGTGTGCT[C/T]CTGAGCGTCTTTTCC | 7011 |
rs192227530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20391480 | TGGAAGCAAATTCAT[A/G]TCATTTATTTCAGTC | 7011 |
rs192295618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20375251 | GACCTCTGCCTCCCG[A/G]GTTCAAGTTATTCTC | 7011 |
rs192376101 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TEP1 | GRCh38.p7 | 14:20409831 | CGAGACCATCCTGGC[C/T]AACACAGTGAAACCC | 7011 |
rs192378710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20385699 | TTTCAATTCTCATAA[C/T]AACCCTCCAATGTCA | 7011 |
rs192553922 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20368735 | TTGCTGTCTTGTGAC[A/T]TCCCTTTGGGATAGG | 7011 |
rs192564692 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414795 | AAGAATGTAACTTAC[C/T]CCCACGCACAATTTT | 7011 |
rs192565492 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TEP1 | GRCh38.p7 | 14:20393095 | GGTGGTGGGTGCCTG[C/T]AGTCCCAGCTACTCG | 7011 |
rs192638760 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415130 | TACTATATGTTTAGA[A/T]ATGTAAATGTTTGTG | 7011 |
rs192644194 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367045 | ATAGATTCTTCCATA[C/T]GATTGAATTTTAGAA | 7011 |
rs192647971 | snp | A/G | 0.00558543 | 0.0525502 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413959 | CATCAGTCAATCAAA[A/G]TTCGCTGAACTGAGA | 7011 |
rs192741156 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20409978 | AGTGAGCCCAGATTG[A/G]CCACTGCACTCCAGC | 7011 |
rs192839670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392402 | GAGTAGTGGTCCCAC[C/T]TAAATAGTATATATA | 7011 |
rs192940418 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | TEP1 | GRCh38.p7 | 14:20387539 | ACTGGGCGACACAGC[A/G]AGACTCCGTCTCAAA | 7011 |
rs193022747 | snp | A/G | 0.000560363 | 0.0167292 | intron-variant | TEP1 | GRCh38.p7 | 14:20373166 | GAGGAGAAAGGACGT[A/G]TTTCATTAGGAGCTG | 7011 |
rs193152744 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20410645 | CAGGGTTCCACTATG[C/T]TGGCCAGGCTGGTCT | 7011 |
rs193205973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20398829 | CTCCCTTTGTAAAGG[A/G]GATGTAAGTCTTATT | 7011 |
rs193276517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20379367 | TGGGGTTACATGGGG[C/T]AGGGGATGACATGAG | 7011 |
rs199500516 | snp | C/T | 4.94898e-05 | 0.00497418 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378193 | ACCCCCCCAGGCACA[C/T]TGAAGGCCAAGGTAC | 7011 |
rs199519079 | snp | G/T | 0.00199792 | 0.0315431 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384505 | CCCCCACTCACAGGG[G/T]TATCTGTGGGCAAAT | 7011 |
rs199552134 | snp | A/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377674 | CCATCTGGGCTGAGT[A/G]CCACAGAGAGGGCAG | 7011 |
rs199556684 | snp | A/G | 1.65655e-05 | 0.00287793 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382290 | CGTGCTCCTTCTCCA[A/G]TGTGCTCAGGATGTG | 7011 |
rs199583487 | snp | C/T | 3.34264e-05 | 0.00408804 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375798 | CCAGTGACCCAGTCA[C/T]GGTGACAGGCAGGGA | 7011 |
rs199583739 | snp | C/T | 1.64871e-05 | 0.00287111 | intron-variant | TEP1 | GRCh38.p7 | 14:20383485 | CCTCCTTCTCACACT[C/T]ACCCGGGGAAGCTTC | 7011 |
rs199599575 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405598 | CATCTGGGAATTGAG[A/G]AAGAGGGAAGAAATG | 7011 |
rs199604556 | snp | A/G | 3.29554e-05 | 0.00405914 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391730 | TCTCTAGGGCCTGTC[A/G]GTACCTGTTCAGCAT | 7011 |
rs199613125 | snp | C/T | 0.000131896 | 0.00811976 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368478 | TGCCCTGCACGTCTC[C/T]CACGGCAAGCTGCAG | 7011 |
rs199624383 | snp | A/G | 5.08117e-05 | 0.00504017 | intron-variant | TEP1 | GRCh38.p7 | 14:20380090 | AGGGAGGAAATAAAC[A/G]AGAGAATGCAAACAG | 7011 |
rs199635567 | snp | C/T | 1.64844e-05 | 0.00287087 | intron-variant | TEP1 | GRCh38.p7 | 14:20373469 | TATTCCGCATACCTT[C/T]CCCACCTCCCTTGAC | 7011 |
rs199659105 | snp | A/G | 0.00379493 | 0.0433943 | intron-variant | TEP1 | GRCh38.p7 | 14:20400958 | GGGAAGAGAAGGAGG[A/G]AATGTGATGGTCAAG | 7011 |
rs199711985 | snp | C/T | 0 | 0 | splice-acceptor-variant | TEP1 | GRCh38.p7 | 14:20378854 | TTAGTCTGCAGCACC[C/T]TATCCCAGGAAGATG | 7011 |
rs199736224 | snp | C/T | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408111 | AGGGTGGCCAGGCAC[C/T]GGTTCTCCAAGGAGA | 7011 |
rs199748092 | snp | C/T | 4.94613e-05 | 0.00497275 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369763 | CTCTCTTCAAACTCT[C/T]CTGATTCCTTTTGCC | 7011 |
rs199849495 | in-del | -/CCAC | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405373 | ACATGAAGCTAGTCA[-/CCAC]CCACCCCGCCACACA | 7011 |
rs199863281 | snp | C/T | 0.00194565 | 0.0311294 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389679 | CGCTGCCAGTAAAGC[C/T]GTTTGGCCACATTTA | 7011 |
rs199881890 | snp | G/T | 0.000131789 | 0.00811648 | intron-variant | TEP1 | GRCh38.p7 | 14:20372726 | TTAACCCATCAGCCT[G/T]TTTCACCTCAAATTT | 7011 |
rs199885544 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387907 | AACACAGACTGACCC[C/T]TGCTGGGAAACAGGA | 7011 |
rs199889885 | snp | C/G/T | 6.59069e-05 | 0.00574019 | intron-variant | TEP1 | GRCh38.p7 | 14:20384547 | AGGTCAGAGCAGGCC[C/G/T]GGCTCCTCTCACCAC | 7011 |
rs199915238 | snp | A/C/G | 0.000462049 | 0.0151934 | intron-variant | TEP1 | GRCh38.p7 | 14:20368564 | AACAGGCCCAGCTAC[A/C/G]ATGGGAACAAAAATA | 7011 |
rs199924635 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant | TEP1 | GRCh38.p7 | 14:20379145 | AGCTCAGGCCATCCC[C/T]TTGACCCTCCAAGTC | 7011 |
rs199929891 | snp | C/T | 4.99846e-05 | 0.00499898 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407923 | TGGATTTCAGGGCTA[C/T]AGGGCAGGTTGAAAG | 7011 |
rs199931942 | snp | C/T | 0.000362355 | 0.0134553 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382630 | GAACTGACCTGCTCA[C/T]ACAGCGTGAAGAGCC | 7011 |
rs199943364 | in-del | -/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405377 | TGAAGCTAGTCACCA[-/C]CCCGCCACACACCAT | 7011 |
rs199976166 | snp | C/G | 0.000148269 | 0.00860886 | missense, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401527 | GAACCAGCTTCTTCA[C/G]GGTGAACCTTGGAGG | 7011 |
rs199992841 | snp | A/G | 0.000516585 | 0.0160632 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371619 | CCTCCTGTAGAATTC[A/G]GTTCAGGTGAAGACT | 7011 |
rs199996170 | in-del | -/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374091 | CATTTTCTTTTTCTC[-/T]TTTTTTTTTTTTTAA | 7011 |
rs200020744 | snp | C/G | 0.00199799 | 0.0315437 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408116 | GGCCAGGCACCGGTT[C/G]TCCAAGGAGAGGATG | 7011 |
rs200043242 | snp | A/G | 6.62306e-05 | 0.00575421 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380441 | TGCAACGTCAGCCTC[A/G]GGGAGCTTTTGTTCC | 7011 |
rs200057042 | snp | A/C/T | 4.94526e-05 | 0.00497235 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382693 | GGCCGGCCTGATTCC[A/C/T]GCTTCACCAGCAGCA | 7011 |
rs200061332 | snp | A/G | 9.90802e-05 | 0.00703778 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378778 | TCCTCCCAAGCACAC[A/G]GTGGCTAGCAGCCGG | 7011 |
rs200120038 | snp | C/T | 0.000176878 | 0.00940255 | intron-variant | TEP1 | GRCh38.p7 | 14:20382366 | AGACACCTAGGATGG[C/T]GGGAGGACAGCCTTG | 7011 |
rs200148837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20385485 | TCAAGCAATTCTCCT[A/G]CCTCAGCCTCCTGAG | 7011 |
rs200164444 | in-del | -/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400569 | CCTCCTCTATTTGAC[-/T]TTTTTTTTTTCTGTA | 7011 |
rs200169501 | snp | A/G | 0.000477952 | 0.0154515 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381335 | TAAGGCAGGTCTCCC[A/G]GAGCCTCAGGAGGGC | 7011 |
rs200181765 | in-del | -/C | 0.000236173 | 0.0108642 | intron-variant | TEP1 | GRCh38.p7 | 14:20374397 | TAGCCCTTCCAGAGA[-/C]CCCCCCAGTGGGATC | 7011 |
rs200198156 | snp | C/G | 2.06158e-05 | 0.00321053 | intron-variant | TEP1 | GRCh38.p7 | 14:20383707 | AGGGGTGGTACGTGG[C/G]CATCAACAAGGCTGG | 7011 |
rs200202466 | snp | C/G/T | 0.000214539 | 0.010355 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373750 | TGCTGGTCAGCTCCA[C/G/T]GCCTTGATGGTCCCA | 7011 |
rs200209294 | snp | A/T | 5.80187e-05 | 0.00538572 | intron-variant | TEP1 | GRCh38.p7 | 14:20396576 | GGCCTCTCCACGTGC[A/T]CATCTAGTTGCTGGG | 7011 |
rs200220209 | snp | C/G | 8.23635e-05 | 0.00641677 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369406 | TGCTGGCATCACTAT[C/G]CATGCTGGCATCAGA | 7011 |
rs200250715 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394672 | TTTAGTAGACAGGGG[A/G]TTTCACCATGTTGGC | 7011 |
rs200275425 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20413009 | AGCACATTTAAGCAC[-/A]GTCTGGGTTTCTATT | 7011 |
rs200318846 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant | TEP1 | GRCh38.p7 | 14:20381405 | TCCAGAGCTGAGCTG[C/T]ATGAACAGATATTGA | 7011 |
rs200345270 | snp | A/G | 1.69304e-05 | 0.00290945 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384072 | TGTCCTGACTGCCCC[A/G]TCACCAGGCTCAGCC | 7011 |
rs200349682 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382672 | GTGACCAAGCGCAGG[C/T]AGAGCGGCCGGCCTG | 7011 |
rs200393958 | snp | A/G | 1.74093e-05 | 0.00295031 | intron-variant | TEP1 | GRCh38.p7 | 14:20395668 | AGTTAGGCAGCTTCT[A/G]TTCCCTCATCTTTTC | 7011 |
rs200437004 | snp | A/G | 0.000710407 | 0.0188335 | intron-variant | TEP1 | GRCh38.p7 | 14:20391116 | TTGGACAAGTGTCAG[A/G]GGAAATAAAGCTCCC | 7011 |
rs200449930 | snp | A/G | 0.000236319 | 0.0108675 | intron-variant | TEP1 | GRCh38.p7 | 14:20395637 | GCAATGCTGTATGAT[A/G]ACAGGTAAATTTCCG | 7011 |
rs200480632 | snp | A/G | 0.000214357 | 0.0103505 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368542 | GCTCACTGACCCTTC[A/G]CATCGGAACAGGCCC | 7011 |
rs200481573 | snp | A/C | 0.000535332 | 0.0163517 | intron-variant | TEP1 | GRCh38.p7 | 14:20377997 | TACTCCTCCTCACAA[A/C]CCACCACCAGCCCTC | 7011 |
rs200484430 | snp | A/T | 0.000198111 | 0.0099507 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382715 | CCAGCAGCAGTCGCA[A/T]CTGGCAAGACTCAGG | 7011 |
rs200508725 | in-del | -/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408844 | TCTTAAAAAAAAAAA[-/C]AACAAAAAGGAATGG | 7011 |
rs200547791 | snp | A/G | 0.00046165 | 0.0151859 | intron-variant | TEP1 | GRCh38.p7 | 14:20381519 | AGGCCCAAGCCCCAC[A/G]CTCAGTGCCCAGGCT | 7011 |
rs200563732 | snp | G/T | 1.65375e-05 | 0.0028755 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368411 | CTCTAGCACAAGGGG[G/T]ATCATTATTCCCGAG | 7011 |
rs200571952 | snp | A/G | 4.94735e-05 | 0.00497336 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405460 | CAATACCTTGAGGAT[A/G]AACTCAGGCTCCAGG | 7011 |
rs200593200 | snp | C/G | 7.45184e-05 | 0.00610358 | intron-variant | TEP1 | GRCh38.p7 | 14:20374572 | GGAGTGGGATTATCA[C/G]CATCCCTCCAGCATT | 7011 |
rs200596242 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397713 | CACTTCCTTATTGTT[C/T]CCTTGTACCTGTGTT | 7011 |
rs200597640 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410801 | TTGTTTCTCCTTTGT[G/T]GTTTTTTTTTTTTTT | 7011 |
rs200604255 | snp | C/T | 0.00101736 | 0.022531 | intron-variant | TEP1 | GRCh38.p7 | 14:20382112 | ACCATACGGTGTCCC[C/T]GCCCCCACCACACCC | 7011 |
rs200605558 | snp | C/G | 0.000369332 | 0.0135842 | intron-variant | TEP1 | GRCh38.p7 | 14:20391109 | GGGCTGATTGGACAA[C/G]TGTCAGGGGAAATAA | 7011 |
rs200606248 | snp | A/G | 8.53526e-05 | 0.00653215 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386457 | CACACCTGTTCCTAC[A/G]GGTCTCCTCCTCAGT | 7011 |
rs200623960 | snp | C/T | 0.000165895 | 0.00910605 | intron-variant | TEP1 | GRCh38.p7 | 14:20387863 | CCCAAGGTTTGACTG[C/T]AGCCCCTCCCAATTC | 7011 |
rs200627369 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391701 | GCTGTGCTTCACAGA[C/G]AGGTTCACAGCTGTC | 7011 |
rs200640923 | snp | C/T | 1.65061e-05 | 0.00287277 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395499 | GCTGCTCATACAACA[C/T]AGGTATCCTCATTGC | 7011 |
rs200650195 | in-del | -/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388459 | TTGAGGGAAATGGAT[-/G]GTATCCAGAGGAAAA | 7011 |
rs200654018 | snp | A/G | 0.00199792 | 0.0315431 | intron-variant | TEP1 | GRCh38.p7 | 14:20382171 | CCCAAGGGAACCAAT[A/G]TAATCCGAACCCTGG | 7011 |
rs200755079 | snp | A/G | 6.59283e-05 | 0.00574106 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406344 | TCCCAAGCTCAGACT[A/G]TAAGAAGGCATTTGG | 7011 |
rs200759401 | snp | A/G | 8.32009e-05 | 0.0064493 | intron-variant | TEP1 | GRCh38.p7 | 14:20384971 | AGCCCCAGCCTGCAG[A/G]CAACAGACAGTACCT | 7011 |
rs200780330 | snp | C/T | 1.6748e-05 | 0.00289374 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380460 | AGCTTTTGTTCCTCT[C/T]TGGGGACTGAAGAAG | 7011 |
rs200791066 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant | TEP1 | GRCh38.p7 | 14:20384515 | CAGGGGTATCTGTGG[A/G]CAAATCAAGCACAAC | 7011 |
rs200824711 | snp | A/C | 1.84449e-05 | 0.00303679 | intron-variant | TEP1 | GRCh38.p7 | 14:20401180 | CTATCATTTCAGAGT[A/C]AGCAAGAAAATAACT | 7011 |
rs200828508 | in-del | -/GATCATAAGTT | 0.0189856 | 0.0955633 | intron-variant | TEP1 | GRCh38.p7 | 14:20412595 | GCTTTACACAAACAG[-/GATCATAAGTT]GATCATAAGTTAGAT | 7011 |
rs200863368 | snp | C/T | 1.65405e-05 | 0.00287576 | intron-variant | TEP1 | GRCh38.p7 | 14:20390793 | TGTTATGTGGTTGCA[C/T]AGTAAGCGACAAACA | 7011 |
rs200869389 | snp | A/G | 8.23716e-05 | 0.00641709 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377636 | TAATGCCATCCGCTC[A/G]ATATCCAACAGCCAC | 7011 |
rs200871389 | snp | C/T | 6.59587e-05 | 0.00574239 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381356 | TCAGGAGGGCAACTT[C/T]GGAAGGTGCCTGAGG | 7011 |
rs200907004 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380939 | ATCTCACCATAGAGG[A/G]CATGGGCCTCCAAGA | 7011 |
rs200915941 | snp | A/G | 3.30218e-05 | 0.00406323 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379973 | ACTGTCCCATTGGCA[A/G]TGCCCACAGCTGCTC | 7011 |
rs200962331 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378392 | TACCTTGGTGACTTT[A/G]AGCCCATCCACCTGG | 7011 |
rs200970310 | snp | A/G | 0.000175973 | 0.00937845 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384039 | CTGAGACTCTGTACC[A/G]GGAAGGCTGTCTTGC | 7011 |
rs200974138 | snp | A/G | 0.000148406 | 0.00861283 | intron-variant | TEP1 | GRCh38.p7 | 14:20377555 | GGGGGCAGGGGCTGC[A/G]CTCTTTCTAAAGGCT | 7011 |
rs200976408 | snp | C/G/T | 0.000181629 | 0.00952804 | intron-variant | TEP1 | GRCh38.p7 | 14:20385112 | GGTACTGCTGGGCCT[C/G/T]CGGGGAGGACAGAGA | 7011 |
rs201001220 | snp | G/T | 1.67565e-05 | 0.00289447 | intron-variant | TEP1 | GRCh38.p7 | 14:20369804 | AATAGGTAATTTTGT[G/T]TAGCCTACCCATATG | 7011 |
rs201018482 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375091 | ACGAAACTCTGTCTC[-/A]AAAACAAAAAAAAAA | 7011 |
rs201018518 | snp | C/T | 6.59935e-05 | 0.0057439 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378141 | TTCTCGCCAGGCCCA[C/T]AGCTCCACCATACTG | 7011 |
rs201034676 | snp | A/C | 1.65427e-05 | 0.00287595 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368404 | TTTGCATCTCTAGCA[A/C]AAGGGGTATCATTAT | 7011 |
rs201047669 | snp | A/G | 6.59055e-05 | 0.00574007 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373370 | AGCACGGACTGGGCC[A/G]CTGTGTCCCAGGAGG | 7011 |
rs201076433 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392486 | TAATGCCCAGTGAAC[-/A]AAAAACAGAAAAACA | 7011 |
rs201084284 | snp | A/G | 2.02321e-05 | 0.00318051 | intron-variant | TEP1 | GRCh38.p7 | 14:20383689 | GGGAGAGAAAAAAAA[A/G]GCAGGGGTGGTACGT | 7011 |
rs201089880 | snp | A/C | 9.88321e-05 | 0.00702896 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408301 | GGCACTGGTTCTTCA[A/C]GGAGAGGATATCTGA | 7011 |
rs201104301 | snp | G/T | 0.00238439 | 0.0344458 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373099 | GAACCATCTGGTGCC[G/T]AAGCCACAGCAGTGA | 7011 |
rs201109558 | snp | A/G/T | 1.64773e-05 | 0.00287026 | intron-variant | TEP1 | GRCh38.p7 | 14:20372696 | AGGAGTGAGGAGACT[A/G/T]CTGTTTCTATCCCAT | 7011 |
rs201138280 | snp | A/C | 3.33428e-05 | 0.00408293 | intron-variant | TEP1 | GRCh38.p7 | 14:20406419 | GGGTAGTAGTGGCAG[A/C]TATGAATCACAGCAG | 7011 |
rs201140993 | snp | C/T | 0.000165115 | 0.0090846 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369774 | CTCTCCTGATTCCTT[C/T]TGCCTCTGTGAAAGA | 7011 |
rs201201116 | snp | A/G | | | | | GRCh38.p7 | 14:20416125 | AAGGAGTCCACACAG[A/G]GCCTTTCTTCTGAAG | 7011 |
rs201206043 | snp | A/G | 0.000267984 | 0.0115724 | intron-variant | TEP1 | GRCh38.p7 | 14:20395990 | ATGAGCACAGGAGCC[A/G]GGAGTATGGGGGGCT | 7011 |
rs201216641 | snp | C/T | 5.47241e-05 | 0.00523059 | intron-variant | TEP1 | GRCh38.p7 | 14:20383158 | CACACCCACCGGCCC[C/T]GGCCTAGAACCCAAC | 7011 |
rs201216772 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20394759 | TCGGCCTCCCAAAGT[C/G/T]CTGGGATTACAGGCG | 7011 |
rs201234352 | snp | A/G | 0.00199792 | 0.0315431 | intron-variant | TEP1 | GRCh38.p7 | 14:20373591 | CTGTCCAGCTGATAA[A/G]ACACAGAGACTGAGT | 7011 |
rs201269445 | snp | C/T | 0.00124282 | 0.0248971 | intron-variant | TEP1 | GRCh38.p7 | 14:20381887 | GCACAGAGAGGTCAG[C/T]GGGAGCTCTGCTGGG | 7011 |
rs201304686 | snp | A/G | 3.29478e-05 | 0.00405867 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403761 | GGTGTCTCTTGGCCC[A/G]GTGCTTCCGAGGGTT | 7011 |
rs201323276 | snp | C/T | 0.000165115 | 0.0090846 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395564 | AACCTCCGCCTGGGA[C/T]GGTTCTTTTCATTTC | 7011 |
rs201332847 | in-del | -/CTT | 0.0164885 | 0.0892882 | intron-variant | TEP1 | GRCh38.p7 | 14:20383441 | CGTGCCGTATCCCTC[-/CTT]CTCCCCAGCCTGCCT | 7011 |
rs201338396 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393799 | TTAAAAAAAAAAAAA[A/G]AGCCAGGGTGCTTAG | 7011 |
rs201340597 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391671 | CAAGACAGTGCGGCC[C/T]GGCAGCAGGGGCAGG | 7011 |
rs201343901 | snp | A/G | 0.00199801 | 0.0315438 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384210 | TCTGGGATGGACACT[A/G]GCTGCTCCAGCAGGG | 7011 |
rs201345072 | snp | G/T | 6.66367e-05 | 0.00577182 | intron-variant | TEP1 | GRCh38.p7 | 14:20389762 | GATGAAAAGGGAGAA[G/T]ATGCTAGAGAAGGGA | 7011 |
rs201372513 | snp | A/G/T | 1.65381e-05 | 0.00287555 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368408 | CATCTCTAGCACAAG[A/G/T]GGTATCATTATTCCC | 7011 |
rs201373338 | in-del | -/A | 0.0603597 | 0.1629 | intron-variant | TEP1 | GRCh38.p7 | 14:20386956 | TTTTTTTTTTGAGAC[-/A]AGAGTTTTGCTCTTG | 7011 |
rs201422723 | in-del | -/C | 0.0603597 | 0.1629 | intron-variant | TEP1 | GRCh38.p7 | 14:20391939 | ACTGGGAGAGAGCTT[-/C]CCTCTGCCCCCATCC | 7011 |
rs201423218 | snp | A/G | 0.000115446 | 0.00759668 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378463 | CCTGCCCCTCTGGGT[A/G]GAAGGCAACACAGTT | 7011 |
rs201424571 | snp | A/G | 0.000242038 | 0.0109982 | intron-variant | TEP1 | GRCh38.p7 | 14:20404817 | TCAGTCACTCCTCCC[A/G]TAGCTTTCTGCCCTG | 7011 |
rs201431531 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20379118 | CTCCTGCGACAGTGG[A/G]TGAGGGAGCGCAGCT | 7011 |
rs201450349 | snp | A/T | 1.65332e-05 | 0.00287512 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368413 | CTAGCACAAGGGGTA[A/T]CATTATTCCCGAGTG | 7011 |
rs201450910 | snp | A/G | 0.000328575 | 0.0128133 | intron-variant | TEP1 | GRCh38.p7 | 14:20377796 | TACCACCTCCACCAC[A/G]CGGTCCTCCTTCCTG | 7011 |
rs201452233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20384245 | AGGCTGAGGGTAAAT[A/G]GGTCAGTGACTATCC | 7011 |
rs201494870 | snp | C/T | 0.000757588 | 0.0194479 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384467 | TCCAGCCCGCCAACA[C/T]AGGGCCGGCCAGCTG | 7011 |
rs201507456 | snp | A/G | 8.24926e-05 | 0.0064218 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378164 | CCATACTGTCCAGCC[A/G]GCCCACAGCCACAAC | 7011 |
rs201526707 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368825 | GGGTCTCTCCCATAG[C/G]TTAACATCTCTGTCC | 7011 |
rs201527652 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20389148 | TAAAAAAAAAAAAAA[-/A]GTGACTGGAGTAGAG | 7011 |
rs201530411 | snp | C/T | 3.30453e-05 | 0.00406467 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382040 | ACACACTCAGCACTC[C/T]GTGCAGCTGGTCCAC | 7011 |
rs201562065 | snp | C/T | 0.00171346 | 0.0292197 | intron-variant | TEP1 | GRCh38.p7 | 14:20381537 | CAGTGCCCAGGCTGA[C/T]TTGGGCTGCAATCAC | 7011 |
rs201568935 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410802 | TGTTTCTCCTTTGTG[G/T]TTTTTTTTTTTTTTT | 7011 |
rs201572632 | snp | C/T | 0.000577906 | 0.0169888 | intron-variant | TEP1 | GRCh38.p7 | 14:20383449 | ATCCCTCCTTCTCCC[C/T]AGCCTGCCTCCCGAC | 7011 |
rs201587210 | in-del | -/C | 0.0138799 | 0.0821421 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20413475 | TGGGAAGGGTGGCAG[-/C]CCGGGGGAGGAGCCG | 7011 |
rs201592628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386671 | GGGATGATTCCCACC[C/T]CCCATCCATAGACAC | 7011 |
rs201609846 | snp | A/G | 0.00199799 | 0.0315437 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408140 | GAGGATGTCTGGGTG[A/G]GCAGAAACATGTCCA | 7011 |
rs201683191 | snp | C/T | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395897 | AGGGCATCAATGGCA[C/T]CATGGGCGTTAAGAA | 7011 |
rs201688770 | snp | C/G | 6.58946e-05 | 0.0057396 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408072 | AACAAGGGGCTGGCA[C/G]ACACAGTGCTCTTTA | 7011 |
rs201690589 | snp | A/C/T | 1.84957e-05 | 0.00304097 | intron-variant | TEP1 | GRCh38.p7 | 14:20383146 | AGATTCACCCCACAC[A/C/T]CCCACCGGCCCCGGC | 7011 |
rs201698574 | snp | A/G | 1.6498e-05 | 0.00287206 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378108 | ATGGTGGGCAGGGAA[A/G]GCAGCCAGCCGTGCC | 7011 |
rs201715559 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373556 | AGCCCGACGGTTACC[A/G]CCAGAAGCTCTGACC | 7011 |
rs201750847 | snp | A/G | 0.000115553 | 0.00760019 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395556 | GGCAAAGAAACCTCC[A/G]CCTGGGACGGTTCTT | 7011 |
rs201759110 | snp | C/T | 1.66186e-05 | 0.00288254 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376118 | CCCGATCCCGGCCCC[C/T]GGTGGCCAGGCTGCC | 7011 |
rs201760641 | snp | C/G | 5.12299e-05 | 0.00506086 | intron-variant | TEP1 | GRCh38.p7 | 14:20395436 | CCCTTGGCTCCCAGA[C/G]AGTGCATACATACCT | 7011 |
rs201793795 | in-del | -/CAAAAA | | | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367362 | AGCCAGACTCTATCT[-/CAAAAA]CAAAAAAAAAAAAAA | 7011 |
rs201794310 | snp | C/G | 0.00227655 | 0.0336614 | intron-variant | TEP1 | GRCh38.p7 | 14:20377535 | AAGACACTTGGGAAG[C/G]GGTAGGGGGCAGGGG | 7011 |
rs201856732 | snp | C/T | 0.00116889 | 0.024147 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372772 | TTCCGCAGTTTCACT[C/T]GCCACTCGCTGATTT | 7011 |
rs201888160 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20371672 | GAGAAAGATCCTATT[G/T]TAGTTAACCTTTCTC | 7011 |
rs201888300 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405602 | TGGGAATTGAGAAAG[A/G]GGGAAGAAATGAGAA | 7011 |
rs201946288 | in-del | -/AAC | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375094 | GAAACTCTGTCTCAA[-/AAC]AAAAAAAAAAAAAAG | 7011 |
rs201959097 | in-del | -/T | 0.0596104 | 0.162024 | intron-variant | TEP1 | GRCh38.p7 | 14:20388458 | GTTGAGGGAAATGGA[-/T]GGTATCCAGAGGAAA | 7011 |
rs201959748 | snp | A/G | 9.88403e-05 | 0.00702925 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382656 | GAGCCTCAGGTGATC[A/G]GTGACCAAGCGCAGG | 7011 |
rs201990502 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382336 | GACAGTGGCAGGCAG[C/G]GTCCGGAGTCTCTCA | 7011 |
rs202032619 | snp | C/T | 0.00128813 | 0.0253457 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381660 | AGCCGGGCACCAGGG[C/T]GCTCCAGAGGGCCCT | 7011 |
rs202032916 | in-del | -/A | 0.419936 | 0.183362 | intron-variant | TEP1 | GRCh38.p7 | 14:20398377 | AGTGAGACTCCGCCC[-/A]AAAAAAAAAAAAAAA | 7011 |
rs202036056 | snp | A/T | 8.24165e-05 | 0.00641883 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378824 | CAGCAGCCAGTGATT[A/T]GGTACTGGTGAGCCT | 7011 |
rs202055706 | snp | A/G | 8.23608e-05 | 0.00641667 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403798 | AGCCAGCTGGTACTC[A/G]TCAAACTGGGCAAAT | 7011 |
rs202061561 | snp | A/G/T | 3.29518e-05 | 0.00405894 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372854 | CACCAATGTGGCCTG[A/G/T]AGCCTGGTGTACACA | 7011 |
rs202080220 | snp | A/G | 8.23893e-05 | 0.00641778 | intron-variant | TEP1 | GRCh38.p7 | 14:20382574 | GACAAAGCAGCTGAA[A/G]AGAGAATGGGAAGTA | 7011 |
rs202085878 | snp | C/T | 0.000399281 | 0.0141238 | splice-acceptor-variant | TEP1 | GRCh38.p7 | 14:20381046 | GTTCCCGCTCTGGAG[C/T]TGAGAAGGTCAGATT | 7011 |
rs202109956 | snp | A/G | 3.30126e-05 | 0.00406266 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378076 | GCATGCAGGAAAAGC[A/G]CAGCAGCAACAAAGC | 7011 |
rs202114016 | snp | C/T | 4.94947e-05 | 0.00497443 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408381 | AGCATAGCCAGGCAC[C/T]GGTTCTCCAAGGAGA | 7011 |
rs202116338 | snp | C/G | 0.00199807 | 0.0315443 | intron-variant | TEP1 | GRCh38.p7 | 14:20373853 | GAGTCATATTGAGCA[C/G]GACATGGGAAACAGA | 7011 |
rs202122820 | snp | C/T | 0.000148791 | 0.008624 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384193 | CCTGGACCAAGTCAT[C/T]GTCTGGGATGGACAC | 7011 |
rs202130386 | snp | A/C | 1.65422e-05 | 0.0028759 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368405 | TTGCATCTCTAGCAC[A/C]AGGGGTATCATTATT | 7011 |
rs202141513 | snp | C/T | 4.9028e-05 | 0.00495092 | intron-variant | TEP1 | GRCh38.p7 | 14:20368769 | GCAGGCGCACGCACA[C/T]ACACACACACACACA | 7011 |
rs202200281 | snp | A/G | 0.000214449 | 0.0103527 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380945 | CCATAGAGGGCATGG[A/G]CCTCCAAGAGCCGAG | 7011 |
rs202201376 | snp | C/T | 0.000638194 | 0.0178519 | intron-variant | TEP1 | GRCh38.p7 | 14:20386046 | TCTTTGCTTCCTCCC[C/T]AGCCCTCCTCCAAAC | 7011 |
rs202226129 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408320 | GAGGATATCTGAGTG[A/G]GTAGATACATGCTGA | 7011 |
rs207474488 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20391249 | AGCTTCAGCAGCCCT[C/T]AGGAGGAGCTGACTG | 7011 |
rs267603922 | snp | A/G | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408307 | GGTTCTTCAAGGAGA[A/G]GATATCTGAGTGGGT | 7011 |
rs367545115 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392301 | AACAATTGGTTCACG[A/C]AAAGATCACCAATGG | 7011 |
rs367549525 | snp | A/G | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382325 | AGCAGCAGGGGGACA[A/G]TGGCAGGCAGGGTCC | 7011 |
rs367562304 | snp | A/G | 4.96356e-05 | 0.0049815 | intron-variant | TEP1 | GRCh38.p7 | 14:20385134 | GGACAGAGACAGTGA[A/G]TTTAGTCCTAGGCCA | 7011 |
rs367568292 | snp | A/G | 0.000147457 | 0.00858527 | intron-variant | TEP1 | GRCh38.p7 | 14:20377798 | CCACCTCCACCACGC[A/G]GTCCTCCTTCCTGTT | 7011 |
rs367573858 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391005 | TTAAGCACTGCAGTC[C/T]TCAGAGTGTCACCTC | 7011 |
rs367578922 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20404410 | CATTTTTTTTTCTCA[A/C]ACTTTGGTCCAGCCC | 7011 |
rs367581679 | snp | C/T | 3.39599e-05 | 0.00412053 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383244 | CTCACCAGCCGGGCC[C/T]GAGCAGAGGCCTCCA | 7011 |
rs367610618 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408157 | CAGAAACATGTCCAT[A/G]TGGTTTCTCCATGGT | 7011 |
rs367790093 | snp | C/G | 2.18333e-05 | 0.00330397 | intron-variant | TEP1 | GRCh38.p7 | 14:20374380 | CGTCTCCCAAAGCCC[C/G]CTTAGCCCTTCCAGA | 7011 |
rs367792138 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384127 | GCACTGTGTCCTGAA[G/T]AAGGCGTGGCCGGGC | 7011 |
rs367826977 | snp | C/T | 0.000313105 | 0.0125082 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378839 | TGGTACTGGTGAGCC[C/T]TAGTCTGCAGCACCC | 7011 |
rs367833588 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20386870 | TTTATATACTTACTG[C/T]TTGTTCATGACAGCA | 7011 |
rs367840800 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368025 | TTCCCGATGAACTGA[A/G]AGGTCTTCCATGCTC | 7011 |
rs367841250 | snp | C/T | 0.000215626 | 0.0103811 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381916 | GGGCACCTGTACCTG[C/T]GCAGACTCTGGACGA | 7011 |
rs367946608 | snp | A/T | 0.000216622 | 0.010405 | intron-variant | TEP1 | GRCh38.p7 | 14:20404800 | GTGAGAGGACTAGAA[A/T]CTCAGTCACTCCTCC | 7011 |
rs367966080 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20394513 | AGACAGAGTCTCACT[C/T]TTGTTGCCCAGGCTG | 7011 |
rs367974917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20404092 | GGTGGCTCACCTTTA[C/T]GCCTGTAATCCCAGC | 7011 |
rs367986961 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20377905 | ACCCCTCTCCCCGTG[G/T]TTCCTGCAATCCAAG | 7011 |
rs368029208 | snp | C/T | 1.67309e-05 | 0.00289226 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371623 | CTGTAGAATTCGGTT[C/T]AGGTGAAGACTAGCT | 7011 |
rs368042308 | snp | C/T | 8.68048e-05 | 0.00658748 | intron-variant | TEP1 | GRCh38.p7 | 14:20379910 | AGAGGGTAAATTCTG[C/T]CCCTCCTTGATTGTC | 7011 |
rs368058247 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20396026 | GGTCCACTCTATTAG[C/T]TTTGTGGGAAGGTAC | 7011 |
rs368068653 | snp | A/G/T | 1.64735e-05 | 0.00286993 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403421 | TGTACCTTGGAAAAC[A/G/T]TCTGTGAGAAAATGG | 7011 |
rs368077042 | snp | A/G | 5.13844e-05 | 0.00506849 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374482 | GGAACTGACCAAGCC[A/G]CTGTCCTGACTCTGG | 7011 |
rs368087056 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20407574 | TCGAACTCCTGGACT[C/G]AAGTGATCCGCCCGC | 7011 |
rs368088692 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401088 | CCAGCTCTGCTAGAA[A/T]CCCAAGGCCCAGGAA | 7011 |
rs368100935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20389133 | AGCCTGAGCGACAGA[A/G]TGAGATTCTGTCTTA | 7011 |
rs368103566 | snp | A/G | 1.71622e-05 | 0.0029293 | intron-variant | TEP1 | GRCh38.p7 | 14:20381711 | TGTGAGGAAGGGAGA[A/G]AGAAGAAGGAAGAGG | 7011 |
rs368104610 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375313 | AGGCATGTGTCACCA[C/T]GCCTGGCTAATTTTG | 7011 |
rs368122891 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409999 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 7011 |
rs368190943 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20369031 | TTTTTTTTTTGAGAC[-/A]AGAGTCTCGCTCTGT | 7011 |
rs368210431 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20379122 | TGCGACAGTGGGTGA[A/G]GGAGCGCAGCTCAGG | 7011 |
rs368221574 | snp | A/G | 0.000380225 | 0.0137829 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384194 | CTGGACCAAGTCATC[A/G]TCTGGGATGGACACT | 7011 |
rs368233990 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant, splice-acceptor-variant | TEP1 | GRCh38.p7 | 14:20404773 | GGCATACAAAGATGC[C/G]TAGGACACAGGGTGA | 7011 |
rs368257268 | snp | C/T | 0.000197655 | 0.00993922 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371290 | GTGGGTGGACAATAT[C/T]ATAGGATTTTCTGTA | 7011 |
rs368264919 | snp | A/C | 4.98016e-05 | 0.00498982 | intron-variant | TEP1 | GRCh38.p7 | 14:20388084 | ATAAATAACAAGATA[A/C]ATGAGAGTAGAATAC | 7011 |
rs368375484 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408059 | CTGTAGACTCTGGAA[C/G]AAGGGGCTGGCAGAC | 7011 |
rs368388916 | snp | C/T | 4.94621e-05 | 0.00497279 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385048 | TGCAGACGTTGGTTC[C/T]GGTTCAGGAACTGCA | 7011 |
rs368480951 | snp | C/T | 5.14258e-05 | 0.00507053 | intron-variant | TEP1 | GRCh38.p7 | 14:20391130 | GGGGAAATAAAGCTC[C/T]CCTGCTTTGGAATTC | 7011 |
rs368485552 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20382511 | GGTATGAGGCGAGGA[C/T]AGGGAGTGGGTGATC | 7011 |
rs368509967 | snp | C/T | 3.30218e-05 | 0.00406323 | intron-variant | TEP1 | GRCh38.p7 | 14:20378332 | GTCTGCCACCCTCCA[C/T]TCCTGTCCTCCTGTG | 7011 |
rs368510757 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TEP1 | GRCh38.p7 | 14:20369165 | GGCACCCGCCACCAC[A/G]CCCAGCTAATTTTTT | 7011 |
rs368511489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20407616 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCG | 7011 |
rs368601784 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375750 | ACCCCTGGCCCTTTA[C/T]TCACCAGTAGGTTAT | 7011 |
rs368614587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388419 | CTGGAGAAGGAGGAA[C/T]GTGCCTGAGGCTTTC | 7011 |
rs368664042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20406155 | CTTCCAACTGGGGAG[A/G]GGACCTGGTTCAAGT | 7011 |
rs368676334 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20378365 | TCCCCCAAGAGCAAC[A/C]CTGGACCTTCTTACC | 7011 |
rs368678828 | snp | A/C | 3.11124e-05 | 0.00394401 | intron-variant | TEP1 | GRCh38.p7 | 14:20386670 | AGGGATGATTCCCAC[A/C]CCCCATCCATAGACA | 7011 |
rs368680818 | snp | A/G | 3.29663e-05 | 0.00405981 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369375 | GTCTTTAGATGTGGT[A/G]TTGGCTCACTATCCA | 7011 |
rs368683348 | snp | A/G | 6.59478e-05 | 0.00574191 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369352 | AACTCACCTTTCTAC[A/G]CTGCCGTGTCTTTAG | 7011 |
rs368691183 | snp | A/G/T | 0.000462111 | 0.0151937 | intron-variant | TEP1 | GRCh38.p7 | 14:20383454 | TCCTTCTCCCCAGCC[A/G/T]GCCTCCCGACACCCA | 7011 |
rs368718343 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20368931 | GGGGAGAGCAGAATG[G/T]TGAGTTCTCAGGGGC | 7011 |
rs368721109 | snp | A/C | 3.29495e-05 | 0.00405877 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391662 | CAGATAGACCAAGAC[A/C]GTGCGGCCTGGCAGC | 7011 |
rs368724046 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20383653 | CAGGCTTCTGTACAT[A/G]GAGAGGAAGTCAGGG | 7011 |
rs368727241 | snp | C/G | 6.59239e-05 | 0.00574087 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403467 | TAGGGACAGGAGAAG[C/G]AATTTCAAAAAAAGG | 7011 |
rs368827794 | snp | C/T | 5.4741e-05 | 0.0052314 | intron-variant | TEP1 | GRCh38.p7 | 14:20404809 | CTAGAATCTCAGTCA[C/T]TCCTCCCGTAGCTTT | 7011 |
rs368830105 | snp | A/G | 0.000280934 | 0.0118485 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382276 | AAGGACATCAGGCCC[A/G]TGCTCCTTCTCCAGT | 7011 |
rs368872757 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20369048 | AGTCTCGCTCTGTCG[-/C]CCAGGCTGGAGTGCA | 7011 |
rs368875202 | snp | A/G | 6.60873e-05 | 0.00574798 | intron-variant | TEP1 | GRCh38.p7 | 14:20378265 | TAGAAATGGAAACGT[A/G]AAGACCTGCTCTCAG | 7011 |
rs368899659 | snp | C/G | 0.00011679 | 0.00764078 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386503 | GTCGATTCCGTGAAG[C/G]CTGATACGGTGAGGG | 7011 |
rs368921557 | snp | C/T | 1.65023e-05 | 0.00287244 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373737 | GAGTGAGCAGGGATG[C/T]TGGTCAGCTCCACGC | 7011 |
rs368981087 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410847 | TTTGTTTTTTGAAAC[A/G]GAGTCTCACTCTATT | 7011 |
rs369002453 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20384305 | CTAAAACTCACAGAG[A/C]CCCCGCCAAGCTACT | 7011 |
rs369052507 | snp | C/T | 4.94694e-05 | 0.00497316 | intron-variant | TEP1 | GRCh38.p7 | 14:20381538 | AGTGCCCAGGCTGAC[C/T]TGGGCTGCAATCACC | 7011 |
rs369100214 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367615 | CTCATCTGGGTAGTT[-/C]TTTTTTTTTTTTTTT | 7011 |
rs369107429 | snp | C/T | 0.000679092 | 0.0184143 | intron-variant | TEP1 | GRCh38.p7 | 14:20382408 | GGGAGGAGAAGCAGC[C/T]TGGCTTGTGGGATAG | 7011 |
rs369151292 | snp | A/G | 3.29495e-05 | 0.00405877 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380291 | TAGTGTGTGTTGGAG[A/G]TGCCATCTCCGGGAG | 7011 |
rs369165576 | snp | C/T | 1.64988e-05 | 0.00287213 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384674 | TGCGGCCTCTTCAGA[C/T]TCAGAAACAAAGTCA | 7011 |
rs369250767 | snp | C/T | 6.59457e-05 | 0.00574182 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368505 | GCAGGGTGGAGTTAG[C/T]GCCCAGCCAAGGTTC | 7011 |
rs369250768 | snp | C/G | 3.38049e-05 | 0.00411112 | intron-variant | TEP1 | GRCh38.p7 | 14:20382111 | AACCATACGGTGTCC[C/G]CGCCCCCACCACACC | 7011 |
rs369290809 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411804 | CTAACAGAATGCTTG[A/T]ATTATACCATCAGGA | 7011 |
rs369383699 | snp | G/T | 1.6525e-05 | 0.00287441 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389612 | TAAGCACCCTTACAG[G/T]TATTGTACCCTTCTT | 7011 |
rs369392288 | snp | A/G | 0.000139889 | 0.00836213 | intron-variant | TEP1 | GRCh38.p7 | 14:20379898 | GCATGGATTTTCAGA[A/G]GGTAAATTCTGCCCC | 7011 |
rs369419136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20398334 | AGTGAGCCGAGGTCG[C/T]GCCATTGCACTCCAG | 7011 |
rs369481352 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405569 | AGAGTAGAGCACAGC[A/G]AGCTCAGTAGAGCCA | 7011 |
rs369496178 | snp | C/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402732 | TGCTCTTAAATGCTA[C/T]GTACAATACCTTATT | 7011 |
rs369530861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20409298 | TCTGACTAGATCTTC[C/T]GAGGGATTCTTTCTC | 7011 |
rs369561408 | snp | G/T | | | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365262 | CCCTCTCTCTTTCTT[G/T]CTTTCTTTTTTTTCT | 7011 |
rs369644051 | snp | C/T | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368465 | AGAAAGTACACATTG[C/T]CCTGCACGTCTCCCA | 7011 |
rs369658008 | snp | C/T | 1.74327e-05 | 0.00295229 | intron-variant | TEP1 | GRCh38.p7 | 14:20386397 | ACCTCAGGTCCACCA[C/T]TCAAGCCCCTCATCC | 7011 |
rs369663832 | snp | C/T | 4.94784e-05 | 0.00497361 | intron-variant | TEP1 | GRCh38.p7 | 14:20381507 | GTCCTGGCCTCCAGG[C/T]CCAAGCCCCACACTC | 7011 |
rs369681398 | snp | C/T | 3.70083e-05 | 0.00430148 | intron-variant | TEP1 | GRCh38.p7 | 14:20383143 | CCCAGATTCACCCCA[C/T]ACACCCACCGGCCCC | 7011 |
rs369759489 | snp | C/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401952 | AGATAAATAGAGAAA[C/T]GAGCACAATGCAGGC | 7011 |
rs369786152 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392240 | TAAAATTCCAGTTAA[A/C]AAATATGCAGGAATG | 7011 |
rs369788833 | snp | G/T | 1.73824e-05 | 0.00294803 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384053 | CAGGAAGGCTGTCTT[G/T]CCCTGTCCTGACTGC | 7011 |
rs369795127 | snp | C/T | 3.2963e-05 | 0.00405961 | intron-variant | TEP1 | GRCh38.p7 | 14:20373437 | ATGGGCTCATGAGAG[C/T]GGGCACAACAGAAGG | 7011 |
rs369824251 | snp | A/C | 9.87781e-05 | 0.00702704 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383765 | TGCTGGGGAGGGCAC[A/C]TGGCTCTTTTAGTTG | 7011 |
rs369833549 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20384357 | CCACCCCATGTCCCT[C/T]TCCATGCCTCTGGTC | 7011 |
rs369842272 | snp | A/G | 3.29609e-05 | 0.00405948 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369570 | CTGGCACACAAAAAT[A/G]AGGACTCTGCCATTT | 7011 |
rs369865662 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20389579 | AGACCACTGATTTCT[A/G]ACACTGGGCAGGAAG | 7011 |
rs369887954 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368895 | GCTGTGACAGAGCCC[A/G]AGTGAATCTCAAAGA | 7011 |
rs369978774 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20385364 | AGACCTTTGATTTTT[A/T]TTTATTTTTTATTTT | 7011 |
rs370020677 | snp | C/T | 3.35858e-05 | 0.00409778 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408423 | TGGGCAGACACATGC[C/T]CATGGAGTTTTTCCA | 7011 |
rs370035144 | snp | A/C | 1.65438e-05 | 0.00287605 | intron-variant | TEP1 | GRCh38.p7 | 14:20378723 | GTCATGGCTCAGGGC[A/C]ACTCTGACCACTGCA | 7011 |
rs370043327 | snp | A/C | 1.66651e-05 | 0.00288657 | intron-variant | TEP1 | GRCh38.p7 | 14:20373816 | CGTGCTCCTCCTGCC[A/C]ACAGAGCACAAGATC | 7011 |
rs370046023 | snp | C/T | 0.00019916 | 0.009977 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378519 | AAGGCCAGCTGCCCA[C/T]GGACTGTGTCCCACA | 7011 |
rs370049348 | snp | A/G/T | 9.95709e-05 | 0.00705525 | missense, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384092 | CAGGCTCAGCCTTCC[A/G/T]TGGGGCAGCATCAGC | 7011 |
rs370051094 | snp | A/C/T | 3.29474e-05 | 0.00405867 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386130 | GGAATGTATCCATAA[A/C/T]GGGAGCCCAGAATCC | 7011 |
rs370085442 | in-del | -/GG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410801 | TTGTTTCTCCTTTGT[-/GG]TTTTTTTTTTTTTTT | 7011 |
rs370100184 | in-del | -/C/CTTT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20369919 | ATCAAGTGCGCAAAT[-/C/CTTT]TTTTTTTTTTTTGAG | 7011 |
rs370150728 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378180 | GCCCACAGCCACAAC[C/T]CCCCCAGGCACATTG | 7011 |
rs370158228 | snp | C/T | 6.59e-05 | 0.00573983 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391033 | CTCCACACAGCACGA[C/T]GTCCACCTGCTCCGC | 7011 |
rs370161233 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388319 | AACTTGCTGTTGGGC[C/T]GGGGCAACGGGGTAG | 7011 |
rs370162854 | snp | A/G | 0.000135872 | 0.00824121 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383245 | TCACCAGCCGGGCCC[A/G]AGCAGAGGCCTCCAG | 7011 |
rs370171359 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TEP1 | GRCh38.p7 | 14:20387677 | ATACGGCCATGATGT[C/T]TGCCGTCATCTTTGC | 7011 |
rs370173278 | snp | G/T | 2.24369e-05 | 0.00334932 | intron-variant | TEP1 | GRCh38.p7 | 14:20368916 | ATCTCAAAGAGGAAA[G/T]GGGAGAGCAGAATGG | 7011 |
rs370190289 | snp | C/T | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415365 | ATCCCATGATTTTCA[C/T]GGTAGTTGCATCCCT | 7011 |
rs370191489 | snp | C/T | 0.0126979 | 0.078662 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414547 | TCTTTTTCCACGATA[C/T]GAGGATACAAGAAAA | 7011 |
rs370193090 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400181 | TTATCTACATATACC[A/G]GCTTCTATCCAGGCC | 7011 |
rs370238754 | snp | C/T | 1.651e-05 | 0.0028731 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380431 | TGCGAAACACTGCAA[C/T]GTCAGCCTCGGGGAG | 7011 |
rs370253145 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393732 | GGGAGGCAGGGGTTG[A/C]AGTGAGCTGAGATCA | 7011 |
rs370370595 | snp | C/T | | | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368849 | TCTGTCCTTCGAAGC[C/T]GTCACCAGCAACTCA | 7011 |
rs370407027 | snp | C/T | 0.000164758 | 0.0090748 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403350 | GATTGTACATGCACA[C/T]ATACAACCCCAGAAG | 7011 |
rs370409037 | snp | A/C | 8.31843e-05 | 0.00644866 | intron-variant | TEP1 | GRCh38.p7 | 14:20384972 | GCCCCAGCCTGCAGG[A/C]AACAGACAGTACCTG | 7011 |
rs370420548 | snp | A/C/T | 8.3192e-05 | 0.00644906 | intron-variant | TEP1 | GRCh38.p7 | 14:20406197 | AACCTCCCCTCCACA[A/C/T]CATTATTAACCTTCC | 7011 |
rs370439177 | snp | A/C | 1.64798e-05 | 0.00287047 | intron-variant | TEP1 | GRCh38.p7 | 14:20377581 | AGGCTCAAAAACCCA[A/C]CCATTCCCATTTCAG | 7011 |
rs370542767 | snp | C/G | 1.75243e-05 | 0.00296004 | intron-variant | TEP1 | GRCh38.p7 | 14:20404578 | GAGAAGGAATGAAGT[C/G]AAGGCCCAAGCTCAG | 7011 |
rs370563255 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20409018 | GAAACAGGTACTTTA[A/G]TCAAGTTGTCAATAT | 7011 |
rs370591761 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20382424 | TGGCTTGTGGGATAG[C/G]GAAGGGGCAGCAGGA | 7011 |
rs370670433 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20410761 | TTTTTTTTTAAGCAT[A/G]TTTGCTTATTAGCCC | 7011 |
rs370712702 | snp | A/C/G | 6.63123e-05 | 0.00575781 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377722 | CCCAGGTGCCCACGG[A/C/G]GCCGACCCAGAGACC | 7011 |
rs370737721 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20390916 | TCATGTATTTTTGGA[C/T]GGTGGGTGTTGAGTG | 7011 |
rs370741178 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376466 | ATAGGACGGGAACGT[A/G]CGGCACTCCCAGCTC | 7011 |
rs370768952 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366882 | GTCAGTGGTTTCAAT[A/C]TTTTGCCTTTTGCTC | 7011 |
rs370824302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20393196 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCG | 7011 |
rs370853183 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369741 | TAAGTTTATATCAAA[A/G]TTCAGCCTCTCTTCA | 7011 |
rs370861793 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373117 | GCCACAGCAGTGACG[A/G]CTGCAGAACTCCTTG | 7011 |
rs370866152 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20382387 | GACAGCCTTGTTCAG[C/T]GCAGTGGGAGGAGAA | 7011 |
rs370870453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386710 | TCACCCTTTAGCACT[A/G]AGCACAAGCCAGGTA | 7011 |
rs370874038 | snp | A/T | 7.59042e-05 | 0.00616006 | missense, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396730 | GGAAGCTTCCCATTT[A/T]CTGTGGAATGTGGGG | 7011 |
rs370880167 | snp | C/G/T | 1.65154e-05 | 0.00287358 | intron-variant | TEP1 | GRCh38.p7 | 14:20390780 | GAAAGAGACTTCATG[C/G/T]TATGTGGTTGCACAG | 7011 |
rs370976102 | snp | C/T | 5.88957e-05 | 0.00542627 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386609 | GATGAAATGAAAAGC[C/T]GGATGCTGCGCCATC | 7011 |
rs370980799 | snp | A/G | 1.6483e-05 | 0.00287076 | synonymous-codon, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381575 | GAGGATGTGTGCCGT[A/G]TCCTCTAGCCCTGGC | 7011 |
rs371028785 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366617 | TAAAGTCCCTCAGGT[C/T]ATTTCTCCATGTAAA | 7011 |
rs371032172 | snp | C/T | 5.98402e-05 | 0.0054696 | intron-variant | TEP1 | GRCh38.p7 | 14:20368747 | GACATCCCTTTGGGA[C/T]AGGTGTGCAGGCGCA | 7011 |
rs371089058 | snp | A/G | 3.30147e-05 | 0.00406279 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384133 | TGTCCTGAAGAAGGC[A/G]TGGCCGGGCAGGACT | 7011 |
rs371092675 | snp | C/T | 0.000283086 | 0.0118938 | intron-variant | TEP1 | GRCh38.p7 | 14:20374383 | CTCCCAAAGCCCCCT[C/T]AGCCCTTCCAGAGAC | 7011 |
rs371127169 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20381491 | GGGAGCACAGTGGGT[A/G]GTCCTGGCCTCCAGG | 7011 |
rs371129295 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393535 | GGTGGCTTACGCCTG[C/T]AATCCCAGTACTTTG | 7011 |
rs371185635 | snp | C/T | 1.66203e-05 | 0.00288268 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373805 | CACAGACACCACGTG[C/T]TCCTCCTGCCCACAG | 7011 |
rs371192226 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374202 | CTCAAGTGATCTCTC[A/G]CCTCAGCCTCCTGAG | 7011 |
rs371194941 | snp | A/G | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381558 | CTGCAATCACCTGCA[A/G]TGAGGATGTGTGCCG | 7011 |
rs371195932 | snp | A/G | 1.65507e-05 | 0.00287664 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384990 | CAGACAGTACCTGAG[A/G]AAGCTGGAATCCCGG | 7011 |
rs371241113 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383855 | GAGCCCCAGAAAAGT[A/G]GAAGAAGACTAATGA | 7011 |
rs371241934 | snp | A/G/T | 3.61554e-05 | 0.00425166 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386594 | ATGTCTCGGAAAGTG[A/G/T]ATGAAATGAAAAGCC | 7011 |
rs371242518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20407166 | ATGTGTAAAAGTGGA[C/T]GTGTATTTGCACATG | 7011 |
rs371252650 | snp | A/G | 3.30524e-05 | 0.00406511 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389249 | TCACTTCAGTATCGC[A/G]TCAGTACAGCCTGAG | 7011 |
rs371337365 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20407584 | GGACTCAAGTGATCC[A/G]CCCGCCTTGGCCTCC | 7011 |
rs371466757 | snp | C/T | 4.94735e-05 | 0.00497336 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381378 | TGCCTGAGGCATCAG[C/T]GTCACATGTCTTCCA | 7011 |
rs371469270 | in-del | -/TAC | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403182 | AAAAAAAAAAAAAAA[-/TAC]AATACCAAGGAGAGT | 7011 |
rs371482888 | in-del | -/TCA | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20396105 | GAAGAAAGAAAAAAG[-/TCA]TCATTTTAGGATGTG | 7011 |
rs371501494 | snp | A/C/T | 0.00016508 | 0.00908376 | intron-variant | TEP1 | GRCh38.p7 | 14:20378937 | GGGGCTTCCAAAAAA[A/C/T]GGGGAAGGCCCTCAT | 7011 |
rs371591018 | snp | C/T | 0.000263544 | 0.0114762 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403401 | CTCTTCTCTGAGAAA[C/T]CCTATGTACCTTGGA | 7011 |
rs371616341 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20377215 | GTGAAGCTCTGTCTT[-/A]AAAAAAAAAAAAAAG | 7011 |
rs371647286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386924 | TCTCCATTTTAGCAA[C/T]CAAGAAACGATAACT | 7011 |
rs371654810 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368246 | TAGAATGTACATATA[C/G]ATACACATAGAATAT | 7011 |
rs371672033 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20385267 | CTAATGTTTTTTATT[C/T]ATTTTTATTTTTTTT | 7011 |
rs371744900 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20404148 | TCACCTGAGGTCAGG[A/C/T]GTTCAAGACCAGCCT | 7011 |
rs371805463 | snp | A/G | 0.00279782 | 0.0372972 | intron-variant | TEP1 | GRCh38.p7 | 14:20377799 | CACCTCCACCACGCG[A/G]TCCTCCTTCCTGTTT | 7011 |
rs371828193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20377921 | TTCCTGCAATCCAAG[C/T]TCCTCCACAGTCTCC | 7011 |
rs371834574 | snp | C/G | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408332 | GTGGGTAGATACATG[C/G]TGATGTAGTTTCTCC | 7011 |
rs371868699 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410377 | AGAGGCTGAGGCAGG[A/C]GGATCACTTGAGCCC | 7011 |
rs371886185 | snp | A/C | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408081 | CTGGCAGACACAGTG[A/C]TCTTTAGACTAGAGA | 7011 |
rs371912038 | in-del | -/TG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372380 | GTGTGTGTGTGTGTA[-/TG]TGTGTGTGTGTGTGT | 7011 |
rs371928449 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20396892 | TAGCAAGACTGTCTC[-/A]AAAAAAAAAAAGCAA | 7011 |
rs371948563 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400782 | ACTACATCTGGTATA[A/G]TGATCTATGATGCCA | 7011 |
rs371964366 | snp | C/T | 1.64963e-05 | 0.00287192 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395878 | ATTTCTGAGTTGAGC[C/T]TCGAGGGCATCAATG | 7011 |
rs372016616 | snp | C/T | 1.65847e-05 | 0.0028796 | intron-variant | TEP1 | GRCh38.p7 | 14:20395973 | CAAAGGAGGGAGGGG[C/T]CATGAGCACAGGAGC | 7011 |
rs372024828 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381001 | AGCCACCACATGGAG[A/G]TTGGTAAGGAACTTC | 7011 |
rs372031810 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369370 | GCCGTGTCTTTAGAT[A/G]TGGTGTTGGCTCACT | 7011 |
rs372051861 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406773 | CCCCAGCAGCCTTGG[C/G]CTGCTTAACCTCTCT | 7011 |
rs372160003 | snp | A/C | 3.40061e-05 | 0.00412333 | intron-variant | TEP1 | GRCh38.p7 | 14:20371643 | GAAGACTAGCTCAAA[A/C]AAGTACATGGACAGA | 7011 |
rs372168444 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant | TEP1 | GRCh38.p7 | 14:20384530 | GCAAATCAAGCACAA[C/T]CAGGTCAGAGCAGGC | 7011 |
rs372170081 | snp | A/G | 1.66738e-05 | 0.00288732 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379944 | CCTGCCAAGTTCTCA[A/G]GTCCAACAGGTAAAC | 7011 |
rs372200434 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387969 | GCCGGAGAGACTGGA[C/T]CCCTGTCTTTCCTGG | 7011 |
rs372203753 | snp | A/C/G | 0.000473484 | 0.0153795 | intron-variant | TEP1 | GRCh38.p7 | 14:20375893 | CCCCAAGGAGAGGGA[A/C/G]CAATCAGGACCAAAG | 7011 |
rs372209391 | snp | A/G | 4.95143e-05 | 0.00497541 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381943 | ACGAGGCAGGCAAAC[A/G]GGCCCATGGGGTAGG | 7011 |
rs372214414 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368429 | CATTATTCCCGAGTG[A/G]CACATCTTCATTCCC | 7011 |
rs372303676 | snp | C/T | 6.60066e-05 | 0.00574447 | intron-variant | TEP1 | GRCh38.p7 | 14:20381415 | AGCTGCATGAACAGA[C/T]ATTGAGAAAGGCTCA | 7011 |
rs372313734 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20373438 | TGGGCTCATGAGAGT[A/G]GGCACAACAGAAGGT | 7011 |
rs372325433 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20368946 | GTGAGTTCTCAGGGG[A/C]CCCTCCTCAGAGAAG | 7011 |
rs372345258 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20369014 | CCTTAGTATTTCTTT[C/T]TTTTTTTTTTGAGAC | 7011 |
rs372394126 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20378270 | ATGGAAACGTGAAGA[A/C]CTGCTCTCAGCAAAA | 7011 |
rs372403985 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20379128 | AGTGGGTGAGGGAGC[A/G]CAGCTCAGGCCATCC | 7011 |
rs372455109 | snp | C/T | | | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365321 | TCTTGTTGCCCAGCC[C/T]GGAGTGCAATGATGC | 7011 |
rs372462628 | snp | G/T | 1.73643e-05 | 0.0029465 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383607 | GGGACTCAGCAGACT[G/T]GGGCAGCAGCCTCTG | 7011 |
rs372483915 | snp | A/G | | | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20384036 | CCCCTGAGACTCTGT[A/G]CCAGGAAGGCTGTCT | 7011 |
rs372514241 | snp | C/T | 0.000133111 | 0.00815708 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384227 | CTGCTCCAGCAGGGC[C/T]CCAGGCTGAGGGTAA | 7011 |
rs372524137 | snp | A/G | 0.00029993 | 0.0122423 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376106 | TTCTGCAGCTCACCC[A/G]ATCCCGGCCCCCGGT | 7011 |
rs372555985 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409398 | CTCACCCACTATGTG[C/G]CTCCAAATGACATTT | 7011 |
rs372627177 | in-del | -/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375096 | AACTCTGTCTCAAAA[-/C]AAAAAAAAAAAAAAG | 7011 |
rs372630237 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20404836 | CTTTCTGCCCTGAAA[C/T]TACTTGCTGATTGAG | 7011 |
rs372638043 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374774 | TATCTGATATGGTGG[G/T]TGTGGGGCTGAGTGC | 7011 |
rs372659024 | snp | C/T | 6.59554e-05 | 0.00574224 | intron-variant | TEP1 | GRCh38.p7 | 14:20381543 | CCAGGCTGACTTGGG[C/T]TGCAATCACCTGCAA | 7011 |
rs372668034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20393790 | TTGTCTCAATTAAAA[A/C]AAAAAAAAGAGCCAG | 7011 |
rs372704689 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390733 | CCAAAAGTATTCAGG[C/G]ACCATCCATCATTTT | 7011 |
rs372718721 | snp | C/T | 5.17522e-05 | 0.00508659 | intron-variant | TEP1 | GRCh38.p7 | 14:20386441 | TCTTCTCTGCAGCCC[C/T]CACACCTGTTCCTAC | 7011 |
rs372753389 | snp | A/C/T | 4.94461e-05 | 0.00497202 | intron-variant | TEP1 | GRCh38.p7 | 14:20373472 | TCCGCATACCTTCCC[A/C/T]ACCTCCCTTGACTCT | 7011 |
rs372780589 | snp | A/G | 0.000345881 | 0.0131461 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403820 | TGGGCAAATTTGTCC[A/G]TCATGGCAGTACGGA | 7011 |
rs372896816 | snp | C/T | 4.95111e-05 | 0.00497525 | intron-variant | TEP1 | GRCh38.p7 | 14:20383461 | CCCCAGCCTGCCTCC[C/T]GACACCCACCTCCTT | 7011 |
rs372939145 | snp | C/T | 9.89348e-05 | 0.00703261 | intron-variant | TEP1 | GRCh38.p7 | 14:20377556 | GGGGCAGGGGCTGCG[C/T]TCTTTCTAAAGGCTC | 7011 |
rs372980013 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402574 | AATCTTTATGACAAC[C/T]TAACAATGTAGGTTC | 7011 |
rs372982338 | snp | A/C/G | 0.000263557 | 0.011477 | synonymous-codon, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380336 | GTGGCAAAGAGGTGA[A/C/G]TCCAGGGGCTGGTTG | 7011 |
rs372989857 | snp | C/T | 0.000197945 | 0.00994651 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389664 | CACTTGGAATTCACA[C/T]GCTGCCAGTAAAGCT | 7011 |
rs373023771 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376490 | CCAGCTCCAGCTCCA[C/T]AGCTCAGGCCGGGAA | 7011 |
rs373024184 | snp | A/G/T | 6.6955e-05 | 0.00578564 | synonymous-codon, stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386526 | GGTGAGGGGCCGCTC[A/G/T]GGCCTGCAGTGCTGG | 7011 |
rs373026039 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20396596 | TAGTTGCTGGGCCCC[A/T]TGGCTACCAGCCCCT | 7011 |
rs373073708 | in-del | -/GC | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410828 | TTTTTTTTTTTTTTT[-/GC]TTTTTGTTTTTTGAA | 7011 |
rs373094993 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20382389 | CAGCCTTGTTCAGTG[C/T]AGTGGGAGGAGAAGC | 7011 |
rs373117609 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414548 | CTTTTTCCACGATAT[A/G]AGGATACAAGAAAAC | 7011 |
rs373182815 | snp | A/G/T | 0.000115433 | 0.00759624 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395532 | TCCGAAGCTGCTGAC[A/G/T]GCTTAGGTGGCAAAG | 7011 |
rs373299312 | snp | C/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402283 | ACTGCACTCCAGCCT[C/G]GGCTACAGAGCAAGA | 7011 |
rs373311646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20410724 | GGATTACAGGTGTGA[A/G]CCACTGTGCCTGGCG | 7011 |
rs373332426 | snp | A/C | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369504 | ATGTTACCTGTGGTC[A/C]ATTCTCCTTCTGGGC | 7011 |
rs373347698 | snp | A/G | 3.29603e-05 | 0.00405944 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378413 | ATCCACCTGGAAGAA[A/G]CTGATGCTGCCAGCC | 7011 |
rs373397069 | snp | A/C/G/T | 4.94233e-05 | 0.00497087 | intron-variant | TEP1 | GRCh38.p7 | 14:20372724 | CATTAACCCATCAGC[A/C/G/T]TGTTTCACCTCAAAT | 7011 |
rs373465446 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392762 | ACCGAGGAATTATTT[G/T]TAGTTTTGTCAGGTA | 7011 |
rs373483093 | snp | C/G | 1.64806e-05 | 0.00287054 | intron-variant | TEP1 | GRCh38.p7 | 14:20372902 | CTTCTGATGAGCCAG[C/G]ATGCACCATCTTTTC | 7011 |
rs373543585 | snp | A/G | 3.31972e-05 | 0.004074 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378520 | AGGCCAGCTGCCCAC[A/G]GACTGTGTCCCACAG | 7011 |
rs373546016 | snp | C/T | 6.6011e-05 | 0.00574466 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395505 | CATACAACACAGGTA[C/T]CCTCATTGCCATCCG | 7011 |
rs373625663 | snp | C/T | 1.6596e-05 | 0.00288058 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381914 | TGGGGCACCTGTACC[C/T]GCGCAGACTCTGGAC | 7011 |
rs373668420 | snp | G/T | 1.74157e-05 | 0.00295085 | intron-variant | TEP1 | GRCh38.p7 | 14:20395667 | GAGTTAGGCAGCTTC[G/T]ATTCCCTCATCTTTT | 7011 |
rs373669828 | snp | A/G | 0.000100257 | 0.00707945 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375811 | CACGGTGACAGGCAG[A/G]GAAGGAGTGGATCAA | 7011 |
rs373687354 | snp | C/G | 3.29516e-05 | 0.00405891 | intron-variant | TEP1 | GRCh38.p7 | 14:20371196 | GAATGTTTGCTTTAG[C/G]ACACACTCAAATAGG | 7011 |
rs373687506 | snp | A/G | 3.3042e-05 | 0.00406447 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384109 | GGGGCAGCATCAGCC[A/G]TTGCACTGTGTCCTG | 7011 |
rs373750998 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388820 | TGCTATGCCTGGATG[A/G]CTGTAAAAGAGGAGT | 7011 |
rs373761192 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20395416 | AGGGTAGCCCCGATT[A/G]CCCACCCTTGGCTCC | 7011 |
rs373793340 | snp | C/T | 0.000167693 | 0.00915524 | intron-variant | TEP1 | GRCh38.p7 | 14:20383128 | CAGGTCCTCATAGCT[C/T]CCAGATTCACCCCAC | 7011 |
rs373824031 | in-del | -/CTTTT | 0.021333 | 0.101051 | intron-variant | TEP1 | GRCh38.p7 | 14:20393488 | AATTGGTGAAATTAA[-/CTTTT]CTTTTCTTTAAGAGA | 7011 |
rs373837405 | snp | C/G/T | 0.00024881 | 0.0111511 | intron-variant | TEP1 | GRCh38.p7 | 14:20374399 | AGCCCTTCCAGAGAC[C/G/T]CCCCAGTGGGATCTC | 7011 |
rs373885587 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20407536 | GGTAGAGACGGGGTT[A/T]CACCATGTTGCCCAG | 7011 |
rs373900934 | snp | A/C/G | 0.00013272 | 0.00814508 | intron-variant | TEP1 | GRCh38.p7 | 14:20386629 | GCTGCGCCATCTGGG[A/C/G]ATAAGCAGAGAGCTG | 7011 |
rs373903999 | snp | C/T | 9.89201e-05 | 0.00703209 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368507 | AGGGTGGAGTTAGCG[C/T]CCAGCCAAGGTTCCA | 7011 |
rs373978178 | in-del | A/GG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20385563 | TTTTTAGTAGAGACA[A/GG]GTTTCACCATGTTGG | 7011 |
rs374000057 | snp | A/G | 3.29647e-05 | 0.00405971 | intron-variant | TEP1 | GRCh38.p7 | 14:20369662 | TCCTCAGGTCCTCCT[A/G]TTACCACTCACCAGA | 7011 |
rs374070269 | snp | C/T | 1.97108e-05 | 0.00313927 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383785 | TCTTTTAGTTGGCCA[C/T]GCAGATAGGTACAGA | 7011 |
rs374082549 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380052 | CCAGAGACAGGCTGG[A/C]GCTAGAGAAAGAGTA | 7011 |
rs374110436 | snp | C/T | 0.000115482 | 0.00759787 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378130 | AGCCGTGCCCCTTCT[C/T]GCCAGGCCCACAGCT | 7011 |
rs374124192 | snp | A/T | 3.30136e-05 | 0.00406273 | intron-variant | TEP1 | GRCh38.p7 | 14:20373222 | AGGCCACCCTTGACC[A/T]TTTTTTGTGCCAGTA | 7011 |
rs374209048 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402733 | GCTCTTAAATGCTAC[A/G]TACAATACCTTATTT | 7011 |
rs374241012 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20370908 | CAAGATGGAGTCCTT[-/G]CCCTCAAGATGCTAT | 7011 |
rs374243036 | snp | A/G | 0.000215612 | 0.0103807 | intron-variant | TEP1 | GRCh38.p7 | 14:20387859 | GTTTCCCAAGGTTTG[A/G]CTGCAGCCCCTCCCA | 7011 |
rs374254590 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406655 | GCTTTCATCTCTTCA[C/T]TGGCGTCACAACCTG | 7011 |
rs374263928 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394738 | CTGCCTCGTGATCCA[A/C]CTGCCTCGGCCTCCC | 7011 |
rs374285934 | snp | C/T | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390749 | ACCATCCATCATTTT[C/T]ATCAAACTCCTGAAG | 7011 |
rs374311707 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377654 | ATCCAACAGCCACCC[A/G]ATCACCATCTGGGCT | 7011 |
rs374314555 | snp | C/T | 0.000720782 | 0.0189703 | intron-variant | TEP1 | GRCh38.p7 | 14:20368751 | TCCCTTTGGGATAGG[C/T]GTGCAGGCGCACGCA | 7011 |
rs374352367 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410630 | ATTTTTAGTAAGAGA[A/C]AGGGTTCCACTATGC | 7011 |
rs374361984 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20391415 | ATAATCCATAAACCT[A/G]GTTGAAACAACATCC | 7011 |
rs374371530 | snp | A/T | 0.000131878 | 0.00811922 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377683 | CTGAGTGCCACAGAG[A/T]GGGCAGGAGAGAGAG | 7011 |
rs374437732 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373043 | CCTTAGCTTCCTGCC[A/G]CAAGATTAGTTCCCC | 7011 |
rs374464557 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391041 | AGCACGACGTCCACC[C/T]GCTCCGCCCTCGTGA | 7011 |
rs374492071 | snp | A/G | 3.31186e-05 | 0.00406918 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384987 | CAACAGACAGTACCT[A/G]AGGAAGCTGGAATCC | 7011 |
rs374493917 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406262 | GGACATGGTCAGTAG[A/G]CTCTGGATGAGATTC | 7011 |
rs374671905 | in-del | -/TAGTAAGTCTCAA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20380563 | ATGGTGTGTCTACAA[-/TAGTAAGTCTCAA]AGTGTGGCCCTCTGG | 7011 |
rs374724679 | in-del | -/TAGA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20395079 | AAAAATACAGAAAGA[-/TAGA]AACAAAAAGAAAAAC | 7011 |
rs374741134 | snp | C/T | 8.32231e-05 | 0.00645016 | intron-variant | TEP1 | GRCh38.p7 | 14:20379109 | AGACTTCTCCTCCTG[C/T]GACAGTGGGTGAGGG | 7011 |
rs374792666 | snp | A/G | 4.94654e-05 | 0.00497295 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401103 | TCCCAAGGCCCAGGA[A/G]GGCGACTTCGAGAAA | 7011 |
rs374805639 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401669 | ATTGTAAGACCATCC[A/G]ATCCCTATGTGGTAA | 7011 |
rs374817029 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386831 | GCTATTTCTTGTACA[A/C]CTCTCTTTTTTCTGG | 7011 |
rs374857354 | snp | C/T | 6.85471e-05 | 0.00585396 | intron-variant | TEP1 | GRCh38.p7 | 14:20371651 | GCTCAAAAAAGTACA[C/T]GGACAGAGAAAGATC | 7011 |
rs374917519 | snp | C/T | 0.000175738 | 0.00937221 | intron-variant | TEP1 | GRCh38.p7 | 14:20396571 | GCAGTGGCCTCTCCA[C/T]GTGCACATCTAGTTG | 7011 |
rs374934480 | snp | C/T | 5.1656e-05 | 0.00508186 | intron-variant | TEP1 | GRCh38.p7 | 14:20382761 | CAGGAGGGCTGCCCG[C/T]AGCCAGCCCTCTGCC | 7011 |
rs374940664 | snp | C/G/T | 0.000110006 | 0.00741566 | intron-variant | TEP1 | GRCh38.p7 | 14:20377797 | ACCACCTCCACCACG[C/G/T]GGTCCTCCTTCCTGT | 7011 |
rs374951845 | snp | C/G | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415477 | CTCACGCCTGTAATC[C/G]CAGCACTTTGGGAGG | 7011 |
rs375047071 | snp | G/T | 0.000477606 | 0.0154459 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408334 | GGGTAGATACATGCT[G/T]ATGTAGTTTCTCCAA | 7011 |
rs375058465 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TEP1 | GRCh38.p7 | 14:20372465 | GCTGGTTTAAATATA[C/T]GCACATTCCTCTACT | 7011 |
rs375059927 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20375429 | AAAGTGCTGGGATTA[C/G]AGGTGTGAGCCACCG | 7011 |
rs375095317 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408018 | TTGTTCACACGGTAC[A/G]AATCAGCTTGCGTCA | 7011 |
rs375126576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374275 | TTATTTTTATTTTTT[A/G]TAGAGATGGGGGGTC | 7011 |
rs375162511 | snp | C/T | 1.6483e-05 | 0.00287076 | intron-variant | TEP1 | GRCh38.p7 | 14:20373453 | GGGCACAACAGAAGG[C/T]TATTCCGCATACCTT | 7011 |
rs375162752 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | TEP1 | GRCh38.p7 | 14:20386243 | CACTGGGGGCATGGT[A/G]TCAGGGAACATAGGC | 7011 |
rs375166652 | snp | G/T | 0.000329984 | 0.0128407 | intron-variant | TEP1 | GRCh38.p7 | 14:20381418 | TGCATGAACAGATAT[G/T]GAGAAAGGCTCAGCC | 7011 |
rs375172392 | snp | C/G | 0.00019923 | 0.00997873 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377322 | AAGTGGCCAGTCCTA[C/G]CACAGGCTTCTGGAA | 7011 |
rs375183937 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409261 | CATGATGCTACTGTC[C/G]TGATTTTCTTCTTAA | 7011 |
rs375193996 | snp | C/T | 3.94228e-05 | 0.00443958 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383772 | GAGGGCACCTGGCTC[C/T]TTTAGTTGGCCACGC | 7011 |
rs375258255 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20386299 | TCGCAACTGAGTAAA[C/G]AAAAGGTAGGCTGCT | 7011 |
rs375260759 | snp | C/G | 3.4456e-05 | 0.00415052 | intron-variant | TEP1 | GRCh38.p7 | 14:20391560 | ATCCCCAGCATTCTA[C/G]CAACCCAACCCCTTG | 7011 |
rs375280462 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408093 | GTGCTCTTTAGACTA[C/G]AGAGGGTGGCCAGGC | 7011 |
rs375292734 | snp | C/T | 0.000132286 | 0.00813176 | intron-variant | TEP1 | GRCh38.p7 | 14:20385128 | CGGGGAGGACAGAGA[C/T]AGTGAGTTTAGTCCT | 7011 |
rs375327446 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20399275 | ATTGCATCCATTGTC[A/G]ACTCAAGTTTTTTCC | 7011 |
rs375392756 | snp | A/G | 8.25689e-05 | 0.00642477 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380432 | GCGAAACACTGCAAC[A/G]TCAGCCTCGGGGAGC | 7011 |
rs375404781 | snp | A/C/T | 0.000115454 | 0.00759704 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368456 | TCCCAATTCAGAAAG[A/C/T]ACACATTGCCCTGCA | 7011 |
rs375452214 | snp | C/G/T | 6.59004e-05 | 0.0057399 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387970 | CCGGAGAGACTGGAC[C/G/T]CCTGTCTTTCCTGGG | 7011 |
rs375457392 | snp | A/C/T | 5.03321e-05 | 0.00501636 | intron-variant | TEP1 | GRCh38.p7 | 14:20384958 | CTTTTGGGGAAGGAG[A/C/T]CCCAGCCTGCAGGCA | 7011 |
rs375488397 | snp | A/G | 9.89903e-05 | 0.00703458 | intron-variant | TEP1 | GRCh38.p7 | 14:20383462 | CCCAGCCTGCCTCCC[A/G]ACACCCACCTCCTTC | 7011 |
rs375542171 | snp | C/G | 3.32182e-05 | 0.00407529 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401609 | CCCCAAGTCCCACAG[C/G]GGTCCTTTCATCCAT | 7011 |
rs375563527 | snp | C/T | 0.000115721 | 0.00760572 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404695 | GTGGGGGCGACACGC[C/T]GGCAAGAAAGCAGCA | 7011 |
rs375591503 | snp | A/C/T | 3.29544e-05 | 0.00405908 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373126 | GTGACGGCTGCAGAA[A/C/T]TCCTTGGTATACATG | 7011 |
rs375738253 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20371370 | AGAGAGGTAAAGAGA[A/C]GAACACCTCTCTTTA | 7011 |
rs375763090 | snp | C/G | 1.67211e-05 | 0.00289142 | intron-variant | TEP1 | GRCh38.p7 | 14:20386051 | GCTTCCTCCCCAGCC[C/G]TCCTCCAAACCTGTC | 7011 |
rs375771751 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366003 | AAACTCCATTTAAAG[A/G]TAAGAACTTGAAGGA | 7011 |
rs375775696 | snp | A/G | 1.64798e-05 | 0.00287047 | intron-variant | TEP1 | GRCh38.p7 | 14:20373415 | CACCTAGGAGGAAGG[A/G]ATGGAGATGGGCTCA | 7011 |
rs375813886 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20395826 | TTGTCAGATGTGGGA[A/G]GCAAAGAGGAGTTGG | 7011 |
rs375820658 | snp | A/G | 6.62252e-05 | 0.00575397 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404653 | GTCAGAAGGCAGCTG[A/G]ACAATGGCACAGAAA | 7011 |
rs375844673 | snp | C/T | 3.29957e-05 | 0.00406162 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379986 | CAGTGCCCACAGCTG[C/T]TCTTTGCCCATTGGT | 7011 |
rs375848101 | snp | A/G | 0.000131985 | 0.0081225 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378131 | GCCGTGCCCCTTCTC[A/G]CCAGGCCCACAGCTC | 7011 |
rs375860266 | snp | A/G | 1.85088e-05 | 0.00304204 | intron-variant | TEP1 | GRCh38.p7 | 14:20383142 | TCCCAGATTCACCCC[A/G]CACACCCACCGGCCC | 7011 |
rs375869483 | in-del | -/CCGCCACA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405379 | AAGCTAGTCACCACC[-/CCGCCACA]CACCATAACCACACT | 7011 |
rs375897230 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20396244 | GAGCCTTAGGCAGGT[A/G]GACTGCCTGGGCTCA | 7011 |
rs375924325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386996 | CTAGAGTAAAATGGC[A/G]CGATCTCGGCTCACT | 7011 |
rs376009278 | snp | C/T | 1.70411e-05 | 0.00291895 | intron-variant | TEP1 | GRCh38.p7 | 14:20395651 | TGACAGGTAAATTTC[C/T]GAGTTAGGCAGCTTC | 7011 |
rs376015778 | snp | A/G | 9.89266e-05 | 0.00703232 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368482 | CTGCACGTCTCCCAC[A/G]GCAAGCTGCAGGGTG | 7011 |
rs376019257 | snp | A/C/T | 0.00113227 | 0.0237688 | intron-variant | TEP1 | GRCh38.p7 | 14:20382109 | CTAACCATACGGTGT[A/C/T]CCCGCCCCCACCACA | 7011 |
rs376025692 | snp | A/G | 4.9629e-05 | 0.00498117 | intron-variant | TEP1 | GRCh38.p7 | 14:20378721 | GAGTCATGGCTCAGG[A/G]CCACTCTGACCACTG | 7011 |
rs376036773 | snp | A/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384059 | GGCTGTCTTGCCCTG[A/T]CCTGACTGCCCCGTC | 7011 |
rs376090362 | snp | A/G | 0.00131314 | 0.0255899 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403315 | AATAGAATTTTGTTC[A/G]TAAATATTAGTCCAG | 7011 |
rs376144459 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403451 | GAGGCTCCATCCCCT[A/G]TAGGGACAGGAGAAG | 7011 |
rs376262631 | snp | A/C | 1.66674e-05 | 0.00288676 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386566 | CCTCAGCAGCAGGTC[A/C]CGCTCCCCATGCATG | 7011 |
rs376297415 | snp | C/G/T | 3.29453e-05 | 0.00405854 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372785 | CTTGCCACTCGCTGA[C/G/T]TTTCTCATCAGCACT | 7011 |
rs376298596 | snp | C/T | 8.23757e-05 | 0.00641725 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384654 | TTCAGTTCTGAGATC[C/T]GACGTGCGGCCTCTT | 7011 |
rs376299827 | snp | A/C/G | 0.000875616 | 0.0209055 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403314 | TAATAGAATTTTGTT[A/C/G]GTAAATATTAGTCCA | 7011 |
rs376305997 | snp | A/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381564 | TCACCTGCAATGAGG[A/T]TGTGTGCCGTGTCCT | 7011 |
rs376320075 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394787 | GCGTGAGCCACCACA[C/T]CCAGCCAGGCTTGAT | 7011 |
rs376327196 | snp | A/C | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403080 | GAGAATCGCTTGAGC[A/C]TGTGAGGTGGAGGTT | 7011 |
rs376330539 | snp | A/G | 0.000267201 | 0.0115555 | intron-variant | TEP1 | GRCh38.p7 | 14:20373824 | TCCTGCCCACAGAGC[A/G]CAAGATCAGAGCAGA | 7011 |
rs376395382 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20381167 | GACTTGAAGAAGAAG[A/G]GCAGGAAAACTGAAA | 7011 |
rs376428773 | in-del | -/AAAAACAAA | | | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367363 | GCCAGACTCTATCTC[-/AAAAACAAA]AAAAAAAAAAAAAGG | 7011 |
rs376431928 | in-del | -/GCGTCCGATTCCCGCA | 0.00716266 | 0.059414 | utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20413410 | GGTGCCTGACCTGGG[-/GCGTCCGATTCCCGCA]GCAGGAAGCAGAAAC | 7011 |
rs376472528 | snp | C/T | 0.000102675 | 0.00716427 | intron-variant | TEP1 | GRCh38.p7 | 14:20391129 | AGGGGAAATAAAGCT[C/T]CCCTGCTTTGGAATT | 7011 |
rs376558769 | snp | C/G | 0.000312961 | 0.0125053 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384400 | GCTGACCTGCAGGTA[C/G]AGCTTCTGGATCATA | 7011 |
rs376564560 | snp | C/T | 1.65146e-05 | 0.0028735 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382266 | AGGCCTGGGGAAGGA[C/T]ATCAGGCCCGTGCTC | 7011 |
rs376572630 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20412607 | ACAGGATCATAAGTT[A/G]GATGCTATTCTGCAC | 7011 |
rs376577795 | snp | C/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401707 | CTTCAAAATAGATTT[C/G]GCCAAGGAGCAGGAA | 7011 |
rs376580636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20387108 | CCTGGCTAATTTTGT[A/G]TTTTTAGTAGAGACA | 7011 |
rs376640551 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392859 | GGTGAAATAAAATGT[G/T]TCTTATTATTTGACA | 7011 |
rs376642082 | snp | C/T | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369555 | AGGATCCCATCAGAG[C/T]TGGCACACAAAAATG | 7011 |
rs376643642 | snp | C/G | 3.29913e-05 | 0.00406135 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381394 | GTCACATGTCTTCCA[C/G]AGCTGAGCTGCATGA | 7011 |
rs376662245 | snp | A/G | 8.19034e-05 | 0.00639883 | intron-variant | TEP1 | GRCh38.p7 | 14:20383703 | AAGCAGGGGTGGTAC[A/G]TGGGCATCAACAAGG | 7011 |
rs376676035 | snp | A/C/G | 5.19398e-05 | 0.00509585 | intron-variant | TEP1 | GRCh38.p7 | 14:20395412 | TGCCAGGGTAGCCCC[A/C/G]ATTGCCCACCCTTGG | 7011 |
rs376720161 | snp | C/G | 5.90127e-05 | 0.00543165 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383789 | TTAGTTGGCCACGCA[C/G]ATAGGTACAGAGGCG | 7011 |
rs376734358 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20369670 | TCCTCCTGTTACCAC[G/T]CACCAGATTCAGGTT | 7011 |
rs376735195 | snp | A/G | 0.000168762 | 0.00918437 | intron-variant | TEP1 | GRCh38.p7 | 14:20375883 | TCTGGATAGGCCCCA[A/G]GGAGAGGGAGCAATC | 7011 |
rs376741158 | in-del | -/TACAATAGTA | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20380558 | ACCATATGGTGTGTC[-/TACAATAGTA]AGTCTCAAAGTGTGG | 7011 |
rs376749010 | snp | A/G | 8.23635e-05 | 0.00641677 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372744 | TCACCTCAAATTTCC[A/G]GGTGCCGAACCCTTC | 7011 |
rs376749495 | snp | A/G | | | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389645 | GAGGATACCAACAAA[A/G]AGGCACTTGGAATTC | 7011 |
rs376771788 | snp | A/G | 5.26404e-05 | 0.00513005 | intron-variant | TEP1 | GRCh38.p7 | 14:20379885 | TTCAGGGCAGTCTGC[A/G]TGGATTTTCAGAGGG | 7011 |
rs376775183 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | TEP1 | GRCh38.p7 | 14:20374583 | ATCAGCATCCCTCCA[A/G]CATTTTGGTATATCT | 7011 |
rs376802805 | snp | A/G | 8.29483e-05 | 0.00643951 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378043 | CCATCCTCTCCAGCC[A/G]TCAGTAACTGGCAAC | 7011 |
rs376808586 | snp | A/G | 1.65116e-05 | 0.00287324 | intron-variant | TEP1 | GRCh38.p7 | 14:20390889 | TCTGGGCTATTCCCA[A/G]GCCTGTGTCCTTCAT | 7011 |
rs376834454 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20371367 | TAAAGAGAGGTAAAG[A/C]GAAGAACACCTCTCT | 7011 |
rs376867679 | snp | A/C/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381592 | CCTCTAGCCCTGGCC[A/C/T]CTTCCCATAGCAACG | 7011 |
rs376871567 | snp | A/C/G | 3.29565e-05 | 0.00405921 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369373 | GTGTCTTTAGATGTG[A/C/G]TGTTGGCTCACTATC | 7011 |
rs376891579 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20387412 | AAAAAATTAGCCGGG[A/C]ATGGTGGCAGGCGCC | 7011 |
rs376900783 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405667 | AGACTAACTTACAAA[C/G]TCAAGGACAGAGAGA | 7011 |
rs376965747 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380390 | GGGGTACTGGCTGAG[A/G]ATTGAAGCCTGCTGC | 7011 |
rs376974676 | snp | A/G | 9.91162e-05 | 0.00703905 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368424 | GGTATCATTATTCCC[A/G]AGTGGCACATCTTCA | 7011 |
rs376987950 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366541 | AGAAGACAGAAGCAT[A/G]GCCTATCAGCGGATG | 7011 |
rs376998078 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397305 | TCAAGGCACAATATC[C/T]ATTTAAAAGAAGGTT | 7011 |
rs376999150 | in-del | -/CGTTTTCAGTAAA/CGTTTTCAGTAAT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400863 | CCTTATAAATCAAAT[-/CGTTTTCAGTAAA/CGTTTTCAGTAAT]ACAACAACCAGGCAA | 7011 |
rs377066506 | snp | A/G | 1.64887e-05 | 0.00287125 | intron-variant | TEP1 | GRCh38.p7 | 14:20381548 | CTGACTTGGGCTGCA[A/G]TCACCTGCAATGAGG | 7011 |
rs377071322 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20382966 | CCCCTCACCCCGAGA[G/T]GCCCTGGAAAGGCCA | 7011 |
rs377075421 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | TEP1 | GRCh38.p7 | 14:20409837 | CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC | 7011 |
rs377093547 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20390560 | GGGTTGTAGCCAGTA[C/G]AGCTGATCTGACTAT | 7011 |
rs377134175 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20380777 | TCTCCTGAGAGTCAC[A/G]TGCTCACCCTCTTGG | 7011 |
rs377147178 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376599 | TGTCACTTCCACCTC[A/G]TGACCTGTGAGGACC | 7011 |
rs377176995 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20380924 | CCCAGCCAGTGACTC[A/G]TCTCACCATAGAGGG | 7011 |
rs377184186 | snp | C/G | 1.64999e-05 | 0.00287222 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373729 | TGGGTCCTGAGTGAG[C/G]AGGGATGCTGGTCAG | 7011 |
rs377196077 | snp | A/G | 3.29506e-05 | 0.00405884 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403833 | CCGTCATGGCAGTAC[A/G]GAGACAGGCGGGCAG | 7011 |
rs377210684 | snp | A/G | 0.000117931 | 0.00767801 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386476 | CTCCTCCTCAGTGAC[A/G]CCCCAGCGGAGGTCG | 7011 |
rs377320599 | snp | C/T | 5.03411e-05 | 0.00501677 | intron-variant | TEP1 | GRCh38.p7 | 14:20378565 | GGAGGAATCAGGATG[C/T]TGAAGAGAGATGCCT | 7011 |
rs377323684 | snp | A/G | 0.000264105 | 0.0114884 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395561 | AGAAACCTCCGCCTG[A/G]GACGGTTCTTTTCAT | 7011 |
rs377379361 | snp | C/G | 4.94319e-05 | 0.00497127 | intron-variant | TEP1 | GRCh38.p7 | 14:20382576 | CAAAGCAGCTGAAGA[C/G]AGAATGGGAAGTAGT | 7011 |
rs377389073 | snp | A/C | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377635 | CTAATGCCATCCGCT[A/C]GATATCCAACAGCCA | 7011 |
rs377395827 | snp | A/G | 4.9458e-05 | 0.00497258 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368522 | CCCAGCCAAGGTTCC[A/G]GGCAGCTCACTGACC | 7011 |
rs377401044 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388126 | ATCAGTGAGGTCTTC[C/T]GAAAAGGGCAGGGGG | 7011 |
rs377410664 | snp | A/G | 3.30759e-05 | 0.00406655 | intron-variant | TEP1 | GRCh38.p7 | 14:20400956 | TGGGGAAGAGAAGGA[A/G]GGAATGTGATGGTCA | 7011 |
rs377413988 | snp | A/C | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414814 | ACGCACAATTTTAAA[A/C]CAAAATTTAAAGACA | 7011 |
rs377424108 | in-del | -/CCC | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392275 | ACCCTCATTCTGCAA[-/CCC]CCGCCAATGAAACAA | 7011 |
rs377447556 | snp | A/G | 1.65225e-05 | 0.00287419 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373775 | GTCCCACACTTTCAA[A/G]GTCCCATCCCGGCTC | 7011 |
rs377507051 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20390440 | GCTTGAAATCAGCCA[C/T]GGTAGGACTGTTTAC | 7011 |
rs377509788 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376366 | GGGCTGAGGGTGACA[C/T]CTGAGGCTCAGCTCC | 7011 |
rs377521252 | snp | C/G | 1.65531e-05 | 0.00287686 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384989 | ACAGACAGTACCTGA[C/G]GAAGCTGGAATCCCG | 7011 |
rs377524296 | snp | A/G | 3.31219e-05 | 0.00406938 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406397 | CTGAATCAAACCAAC[A/G]ACCCTGGGGTAGTAG | 7011 |
rs377578821 | snp | A/T | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415142 | AGATATGTAAATGTT[A/T]GTGTATAACATTCAA | 7011 |
rs377614240 | snp | A/C/G | 1.64741e-05 | 0.00286998 | missense, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384396 | TTCTGCTGACCTGCA[A/C/G]GTAGAGCTTCTGGAT | 7011 |
rs377659153 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20412146 | GACAACAATATCTCA[C/T]TGGACGTCAGTGTGA | 7011 |
rs377660135 | snp | A/C/G | 9.98293e-05 | 0.0070644 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384711 | CAGGCATCTGGCACA[A/C/G]AGCTGACCACCAAAG | 7011 |
rs377744214 | snp | A/G/T | 5.30474e-05 | 0.00514989 | intron-variant | TEP1 | GRCh38.p7 | 14:20382367 | GACACCTAGGATGGC[A/G/T]GGAGGACAGCCTTGT | 7011 |
rs377745887 | snp | C/T | 0.000309915 | 0.0124443 | intron-variant | TEP1 | GRCh38.p7 | 14:20396587 | GTGCACATCTAGTTG[C/T]TGGGCCCCATGGCTA | 7011 |
rs377746806 | snp | A/G | 1.64969e-05 | 0.00287196 | intron-variant | TEP1 | GRCh38.p7 | 14:20390761 | TTTCATCAAACTCCT[A/G]AAGGAAAGAGACTTC | 7011 |
rs377747167 | snp | C/T | 1.64849e-05 | 0.00287092 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373092 | TGCCATGGAACCATC[C/T]GGTGCCCAAGCCACA | 7011 |
rs386380811 | in-del | -/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20369925 | TGCGCAAATTTTTTT[-/T]TTTTTTGAGACGGAG | 7011 |
rs386775290 | multinucleotide-polymorphism | CA/TG | | | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365366 | GCAACCTCTGCCCCC[CA/TG]AGTTCAAGCGATTCT | 7011 |
rs386775291 | multinucleotide-polymorphism | CG/TA | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366388 | GATGATGCCATGCCA[CG/TA]GTTCGCTGCAGGATT | 7011 |
rs386775292 | multinucleotide-polymorphism | AA/GC | | | intron-variant | TEP1 | GRCh38.p7 | 14:20369120 | TCACACCATTCTCCT[AA/GC]CTCAGACTCCCGAGT | 7011 |
rs386775293 | in-del | -/AT/GTC/T/TT | 0.341673 | 0.232586 | intron-variant | TEP1 | GRCh38.p7 | 14:20369918 | CAATCAAGTGCGCAA[-/AT/GTC/T/TT]TTTTTTTTTTTTGAG | 7011 |
rs386775294 | in-del | ACCATAACCCACCACACACCCA/CG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405380 | AGCTAGTCACCACCC[ACCATAACCCACCACACACCCA/CG]CCACACACCATAACC | 7011 |
rs397756124 | in-del | -/G | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20370241 | CTTAAATGTACATCG[-/G]CGATGTATTTTTACA | 7011 |
rs397853201 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398518 | ATTAAAAAAAAAAAA[-/A]GAGTGAAGGGGTGAC | 7011 |
rs397959120 | in-del | -/AAA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20387562 | TCTCAAAAAAAAAAA[-/AAA]GAAATTAAGCAACTA | 7011 |
rs527268021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20387319 | TGGGAGGTCGAGGCG[C/G]GCAGATCACCTGAGG | 7011 |
rs527306219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386940 | CAAGAAACGATAACT[C/T]TTTTTTTTTTTGAGA | 7011 |
rs527359921 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20416227 | CTGTGACTCTCTGTG[A/G]GAAACACCTGCCCCA | 7011 |
rs527385879 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415502 | GGGAGGCCAAGGTGG[A/G]CAGATTACCTGAGGT | 7011 |
rs527427324 | snp | A/G | 3.36995e-05 | 0.00410471 | intron-variant | TEP1 | GRCh38.p7 | 14:20375873 | CAGAGGAGACTCTGG[A/G]TAGGCCCCAAGGAGA | 7011 |
rs527468705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20410662 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTTGT | 7011 |
rs527472833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20404298 | AGGCGGAGGTTGCAG[C/T]GAGCCGAGATCACGC | 7011 |
rs527510376 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20376392 | GCTCCATGGGAGGGA[A/T]GCAGGGAGTCACAAG | 7011 |
rs527535560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20399398 | TTTATCCTTAAGATT[G/T]CAAAATTCACTAATT | 7011 |
rs527772763 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20370282 | CCCATGCAGTCACCC[A/G]ACAGATCAAGATGTA | 7011 |
rs527788671 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20396794 | CACAGTGGCATGCAC[A/C]TATAATCTCAGCTAC | 7011 |
rs527816839 | in-del | -/TT/TTT | 0.254944 | 0.249951 | intron-variant | TEP1 | GRCh38.p7 | 14:20410599 | GCTGATTTTTTTTTC[-/TT/TTT]TTTTTTTTTTTTTGT | 7011 |
rs527822925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20394555 | CGCGATCTCAGCTCA[C/T]AGCAACCTCCGCCTC | 7011 |
rs527873149 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382649 | GCGTGAAGAGCCTCA[A/G]GTGATCGGTGACCAA | 7011 |
rs527904744 | snp | C/T | 1.65682e-05 | 0.00287817 | intron-variant | TEP1 | GRCh38.p7 | 14:20382725 | TCGCATCTGGCAAGA[C/T]TCAGGACTCAGGGTG | 7011 |
rs527927823 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | TEP1 | GRCh38.p7 | 14:20407004 | CTAAAGGGTTAAGAG[G/T]TTGCCCAAGGTTGCA | 7011 |
rs527947652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411332 | GGTATCTCTTGACTA[C/T]GGGCCTGTGCACAGG | 7011 |
rs527964420 | snp | C/T | 1.65102e-05 | 0.00287312 | intron-variant | TEP1 | GRCh38.p7 | 14:20378340 | CCCTCCACTCCTGTC[C/T]TCCTGTGCTTCCCCC | 7011 |
rs528129649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401932 | AAATCACTAAGACTC[C/T]TAATAGATAAATAGA | 7011 |
rs528153523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20390392 | TCCTGAGCGTCTTTT[C/T]CCAACTCTATGTTCA | 7011 |
rs528233605 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409150 | TTCTTACTCCCATAA[A/G]TAAATATATCTTGGC | 7011 |
rs528260871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20385824 | GATCAGTACCCAGAT[A/C]TATCTGATGGCAACA | 7011 |
rs528273144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20384917 | TATACTCTGAATACT[A/G]AGGAGAGAAGACTGG | 7011 |
rs528274680 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20390857 | GAACTGTGTATTGTC[G/T]GTGCCTTTACCAAAT | 7011 |
rs528351369 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414091 | GATGGAACCAGGCTT[A/T]GGAAAGAGACAAGTG | 7011 |
rs528397757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20380531 | ACCCCATTAGCCCCA[A/G]CACCAAATAAAACCA | 7011 |
rs528443455 | in-del | -/A | 0.00202418 | 0.0317489 | intron-variant | TEP1 | GRCh38.p7 | 14:20379901 | GGATTTTCAGAGGGT[-/A]AAATTCTGCCCCTCC | 7011 |
rs528621660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20369156 | GGGACTACAGGCACC[C/T]GCCACCACGCCCAGC | 7011 |
rs528669607 | snp | A/G | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414048 | CTGGAGCCATCCTGA[A/G]TGATTAATGCTGAAC | 7011 |
rs528674253 | snp | A/G | 0.000230601 | 0.0107353 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403764 | GTCTCTTGGCCCGGT[A/G]CTTCCGAGGGTTGTA | 7011 |
rs528685127 | snp | A/C | 1.71876e-05 | 0.00293147 | intron-variant | TEP1 | GRCh38.p7 | 14:20391565 | CAGCATTCTACCAAC[A/C]CAACCCCTTGGAGGA | 7011 |
rs528845054 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20371148 | CCTATCCTCCATGAC[A/G]GGCCCCAAGGTGTAA | 7011 |
rs528930158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20405311 | CACAGGGACTAGGCC[A/G]CAGACTCACCCAGAA | 7011 |
rs528966544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411286 | TCTAAGCTTCAATCA[C/T]ACAAATTTTATTTAG | 7011 |
rs529037264 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20371857 | ACATTCTTGGCTTTT[C/T]CTTCCCTCTCTACCT | 7011 |
rs529064458 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366569 | ATGTCATCATCCTCT[A/G]GTCAGGATGGAAACC | 7011 |
rs529088324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20405822 | AGTTCGAGAGCAGCC[C/T]GGCCAACATGGCGAA | 7011 |
rs529114338 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366928 | CCAAGGGCAGGAGGA[A/T]GCTCTAGTTGTCTGT | 7011 |
rs529152071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20395268 | ACTTTGTTTCATGAT[C/T]TCTCTTTAGGACAAT | 7011 |
rs529292418 | snp | A/G | 0.000121291 | 0.00778656 | intron-variant | TEP1 | GRCh38.p7 | 14:20383734 | CTGGGCTCATTGGGG[A/G]ATACCCACCGGTAGG | 7011 |
rs529294427 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20389455 | CAGAGGGGTACAGAG[A/T]TAGGCTAAAGTATCC | 7011 |
rs529308451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20389004 | AATACAAAAATTAGC[C/T]GGGCATGGTGGTGCA | 7011 |
rs529365357 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411461 | TCCTCCAAAAAGCCT[A/G]TGCTGACACCAAGCC | 7011 |
rs529445081 | snp | A/G/T | 8.24349e-05 | 0.00641965 | intron-variant | TEP1 | GRCh38.p7 | 14:20373229 | CCTTGACCTTTTTTT[A/G/T]TGCCAGTAACACACC | 7011 |
rs529570419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20413217 | CCCTCCCCTTCCCGG[A/C]GCCGCCGGGAGGAGC | 7011 |
rs529598159 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373692 | CCTGCACGGGGCTCC[A/G]TGGCAGCTGCACAGT | 7011 |
rs529705136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20391991 | ACTCATGGTAGGAGA[G/T]GGGAAGTCACCTGTA | 7011 |
rs529774498 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388860 | CACTTTAAAAAAGAA[G/T]TAACTGGAGCCGGGT | 7011 |
rs529843171 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386918 | TCATTATCTCCATTT[A/T]AGCAATCAAGAAACG | 7011 |
rs529864179 | snp | A/G | 1.65899e-05 | 0.00288005 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381915 | GGGGCACCTGTACCT[A/G]CGCAGACTCTGGACG | 7011 |
rs529904736 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20383415 | ACCACATTGGAGAGG[A/C]CTCTCTCCTCCGTGC | 7011 |
rs529915473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20370275 | GCATCCACCCATGCA[A/G]TCACCCGACAGATCA | 7011 |
rs529974379 | snp | C/T | 1.64936e-05 | 0.00287168 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403870 | CAGCTTATTCTTATC[C/T]CCCTCAGCCAGGCTC | 7011 |
rs529977342 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20369886 | AATTTTTTTTTTTTT[A/T]AACTACAACTTAGAT | 7011 |
rs529990392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409937 | TGAGGCAGGAGAATG[A/G]CGTGAACCAGGGAGG | 7011 |
rs530020918 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372911 | AGCCAGGATGCACCA[C/T]CTTTTCCCTCCCAGG | 7011 |
rs530025246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20409787 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 7011 |
rs530093129 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20370197 | GGGATTACAGGCGTG[A/G]GCCACTACACCTGGG | 7011 |
rs530123286 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20396734 | GCTTCCCATTTTCTG[A/T]GGAATGTGGGGCATA | 7011 |
rs530167793 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20399964 | GTCAGGAGTTCAAGA[C/T]CAGCCAATATGGTGA | 7011 |
rs530223447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20387837 | CAGCTAGAATTTCAG[C/T]CCCAGGGTTTCCCAA | 7011 |
rs530233568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20387442 | CTGTAGTCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 7011 |
rs530235532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20393529 | AGGCATGGTGGCTTA[C/T]GCCTGTAATCCCAGT | 7011 |
rs530351081 | snp | C/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402876 | AGTAAAGTACAATAC[C/T]AGCTGGGTGTGGTGG | 7011 |
rs530356778 | snp | A/G | 4.94336e-05 | 0.00497135 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382678 | AAGCGCAGGTAGAGC[A/G]GCCGGCCTGATTCCC | 7011 |
rs530399685 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367086 | GTTCTTTTATGGGCC[A/G]GGCACAATGGCTCAC | 7011 |
rs530452897 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388916 | GCACTTTGGGAGGCT[A/G]AGGTGGGTGGATCAC | 7011 |
rs530483758 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411233 | CGGTCACCTCCCAGC[A/T]TCATCTCTCACTAAC | 7011 |
rs530521388 | snp | C/T | 1.65037e-05 | 0.00287256 | intron-variant | TEP1 | GRCh38.p7 | 14:20401453 | TCAGGGTGCAGCTTC[C/T]CACCTGTAACCCAGC | 7011 |
rs530561169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20406746 | GAAAAAGGGCAAAGC[C/G]CCATATTAATCCCCC | 7011 |
rs530605336 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20373170 | AGAAAGGACGTGTTT[C/T]ATTAGGAGCTGGGAT | 7011 |
rs530624842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396142 | AAGGTAACAAAAGAA[A/G]AGAAAGTAACAGAAG | 7011 |
rs530828217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20385585 | ACCATGTTGGCCAGG[C/G]TGGTCTCAAACTCCT | 7011 |
rs530861644 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20413411 | GTGCCTGACCTGGGG[C/T]GTCCGATTCCCGCAG | 7011 |
rs530864318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20384828 | AGTAGAGAGCTCCTG[A/C]CTCCAGCACCAAGGC | 7011 |
rs530879837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20373943 | GAACTCAGGAACAGT[A/G]GGGTTGGGTGGCTCA | 7011 |
rs531251559 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20416317 | AGAAGACTGGCAATA[C/T]AGGAGGGAAGGCAAT | 7011 |
rs531278635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20410722 | TGGGATTACAGGTGT[A/G]AGCCACTGTGCCTGG | 7011 |
rs531429813 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403030 | AGCGTGGTGGCACAC[A/G]CCTGTAGTCCCAGCT | 7011 |
rs531445057 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20410200 | AATTCTATTGATTCT[A/C]CTCCCTCAGTGTCTC | 7011 |
rs531483684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20370500 | AATGTCTACGAGGTA[C/T]GTCTGTATTATTCCA | 7011 |
rs531508859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20371776 | TGTTCCACTTTCTGG[C/T]TTTTGTTTTTTAACA | 7011 |
rs531645415 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20365752 | GTTACTCTCAACTTC[C/T]GTACTTATCTCATTA | 7011 |
rs531731738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395145 | GAATCAGAGCAGAAG[C/G]AGAGAGGACACCAGC | 7011 |
rs531744124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20394640 | ACCCACCACCACACC[C/T]GGCTAATTTTTGTAT | 7011 |
rs531746468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20383406 | AAAAGGAGAACCACA[A/T]TGGAGAGGCCTCTCT | 7011 |
rs531796942 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20377035 | AGCATGACCAACATG[A/G]TGAAACCCCATCTCT | 7011 |
rs531874404 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20388898 | CTCACGCCTGTAATC[C/G]CAGCACTTTGGGAGG | 7011 |
rs531882956 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20406095 | AAAAAAGAAAAGGGG[A/T]TTAGGAAGTGAGAAA | 7011 |
rs531891774 | snp | A/G | 3.29647e-05 | 0.00405971 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378393 | ACCTTGGTGACTTTG[A/G]GCCCATCCACCTGGA | 7011 |
rs531897085 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366722 | ACCAGGGTGTAGTGG[C/T]ATTTCTCCAAGAGAA | 7011 |
rs531998001 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20378918 | CTCCTCATTTCCTTC[C/T]CCTGGGGCTTCCAAA | 7011 |
rs532050555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411928 | GACCAGCCTGGGCAA[C/T]ATAGTGAGACCTCTA | 7011 |
rs532053933 | in-del | -/GGTTTTTTTTTT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410801 | TTGTTTCTCCTTTGT[-/GGTTTTTTTTTT]TTTTTTTTTTTTTTT | 7011 |
rs532063206 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402857 | TACTGACATGTCACC[C/T]GGCAGTAAAGTACAA | 7011 |
rs532130327 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390994 | CTTCTTCTGCCTTAA[A/G]CACTGCAGTCTTCAG | 7011 |
rs532194975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380591 | AGTGTGGCCCTCTGG[C/T]CCTATATCAGGAATA | 7011 |
rs532266109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20385880 | TTGCTCATGGCCAAC[C/T]CCAGAGGCACTTCTC | 7011 |
rs532322125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20375234 | CTGGAGTGCAATGGC[A/G]CGACCTCTGCCTCCC | 7011 |
rs532372748 | snp | A/C/G | 0.000115902 | 0.00761174 | intron-variant | TEP1 | GRCh38.p7 | 14:20369782 | ATTCCTTTTGCCTCT[A/C/G]TGAAAGAATAGGTAA | 7011 |
rs532415757 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415408 | GTGTATTAAAACTAC[A/G]CATAAAATGCCTTGT | 7011 |
rs532418954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20369254 | ACCTCATTATCTGCC[C/T]GCCTAGGCCTCCCAA | 7011 |
rs532426853 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20377169 | GCAGTGAGCCGAGAC[C/T]GTACCACTGCACTCT | 7011 |
rs532428895 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402701 | TCAAAGCCGGGTGAC[A/G]TGAATCCAGATTCTA | 7011 |
rs532430912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20409756 | CCGGGCGCGGTGGCT[C/T]ACGCCTGTAATCCCA | 7011 |
rs532439478 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20398533 | AGAGTGAAGGGGTGA[A/C]ATTAATGCCCTCAGA | 7011 |
rs532457297 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414800 | TGTAACTTACCCCCA[C/T]GCACAATTTTAAACC | 7011 |
rs532569714 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403393 | TTTCTCTGCTCTTCT[C/T]TGAGAAACCCTATGT | 7011 |
rs532585466 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20399091 | AGAGACGGGGTTTCA[A/C]CATGTTGCTCAGGCT | 7011 |
rs532602316 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20373668 | GGGGAGGTGGCTGAC[A/G]TTTTGTTACCTGCAC | 7011 |
rs532728221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20387409 | AAAAAAAAATTAGCC[A/G]GGCATGGTGGCAGGC | 7011 |
rs532735886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20386997 | TAGAGTAAAATGGCG[C/T]GATCTCGGCTCACTG | 7011 |
rs532791615 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402281 | CACTGCACTCCAGCC[-/TG]TGGGCTACAGAGCAA | 7011 |
rs532816091 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409824 | AGGAGATCGAGACCA[C/T]CCTGGCTAACACAGT | 7011 |
rs532913465 | snp | C/G | 8.23621e-05 | 0.00641672 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372759 | GGGTGCCGAACCCTT[C/G]CGCAGTTTCACTTGC | 7011 |
rs532969378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395340 | GAGCCACTGCGATGA[C/T]TGACAAGCAAACCTT | 7011 |
rs532973809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20411837 | CTATTTTCTGGCTGG[A/G]TGTGGTGGCTCACAC | 7011 |
rs532975457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20401366 | TAAAGTCATGTTGCT[A/G]GGTTTGAGAACTACT | 7011 |
rs532978860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20389048 | AGGTACTCGGGAGGC[A/G]GAGGCAGGAGGATCG | 7011 |
rs533073543 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20370094 | GATTTTTTTATTTTT[A/G]GTAAAGATGGGGTTT | 7011 |
rs533271669 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20412727 | TCTGGCTCTGTTGTT[C/G]AGCTCACTGCAATCT | 7011 |
rs533292048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20389472 | AGGCTAAAGTATCCA[C/T]CTGAAGTGCAACAGA | 7011 |
rs533431433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20413367 | GCCTGCGCTCGGACC[C/G]TACCTTAGACTGGGG | 7011 |
rs533513159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20375436 | TGGGATTACAGGTGT[A/G]AGCCACCGTGCCCAG | 7011 |
rs533514179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20379872 | GCTCATCTAGGGCTT[C/G]AGGGCAGTCTGCATG | 7011 |
rs533558672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401974 | AATGCAGGCTACGAG[A/G]AGTTTAAAAACTAAA | 7011 |
rs533594698 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415010 | CCATACCACCCCGAA[C/T]GCGCCCGATCTCCTC | 7011 |
rs533622232 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402505 | GGTAGTGATAGCTAA[C/T]ACTTATTTACTTCCA | 7011 |
rs533638369 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20399082 | TTTTTGGTTAGAGAC[A/G]GGGTTTCACCATGTT | 7011 |
rs533654982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409250 | CCTTTGCTTTCCATG[A/G]TGCTACTGTCCTGAT | 7011 |
rs533792806 | snp | A/G | 0.000164894 | 0.00907854 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381379 | GCCTGAGGCATCAGC[A/G]TCACATGTCTTCCAG | 7011 |
rs533818702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392585 | GGTTTTCACAGTAGC[C/T]CAATGCCATAAGAAC | 7011 |
rs533851593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409816 | ACAAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT | 7011 |
rs534025721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20398014 | TGCCTCGGCCTCCCA[A/C]ATTGCTGGGATTACA | 7011 |
rs534064483 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20382471 | TGAAAAAGTAAAGAA[C/T]AACAGTAGGAGGGAA | 7011 |
rs534087161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20377128 | GCCGAGACAGGAGAA[C/T]TGCTTGAACCCAGGA | 7011 |
rs534169508 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20410399 | CTTGAGCCCAGGAGT[G/T]TAAAACCAGCCTGAG | 7011 |
rs534208856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392989 | TTTAGGAGGCCGAGG[C/T]GGGCAGATCACAAGG | 7011 |
rs534213792 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20390385 | AGTGTGCTCCTGAGC[A/G]TCTTTTCCCAACTCT | 7011 |
rs534317738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20389795 | CTAGACAGCCCAGGA[A/C]ATTAAGATATGAGCT | 7011 |
rs534325400 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367848 | TCTCCTGACCTCGTG[A/T]TCTGCCCACCTCGGC | 7011 |
rs534333801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395801 | AATATTGGTGCTGCT[C/G]CTTCATTTATTGTCA | 7011 |
rs534496541 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415430 | ATGCCTTGTGTTTAT[A/G]TTTAAAATTAAATTA | 7011 |
rs534553703 | snp | C/T | 0.00478085 | 0.0486577 | | | GRCh38.p7 | 14:20416592 | TTGAAACTCAATCTG[C/T]GATGTGATAATATTA | 7011 |
rs534555998 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371221 | AATAGGACTTACCAA[A/G]AAAGAAAGAACTCCA | 7011 |
rs534640298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374236 | CTAGAACTACAGGCA[C/T]GTACCATGGTACCCA | 7011 |
rs534687859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402613 | TTCCCATTTAATACG[C/T]GAGAAAACTGAGGCA | 7011 |
rs534712333 | in-del | -/G | 0.00716266 | 0.059414 | intron-variant | TEP1 | GRCh38.p7 | 14:20385563 | TTTTTAGTAGAGACA[-/G]GGTTTCACCATGTTG | 7011 |
rs534723707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402134 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAACT | 7011 |
rs534781851 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20396956 | AGCAAGAAGTTCAGA[A/C]ACCAGGCATGTGGAA | 7011 |
rs534804309 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405372 | CAACATGAAGCTAGT[C/T]ACCACCCCGCCACAC | 7011 |
rs534857405 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20412948 | ACAGGCGTGAACCAC[C/G]GCGCCCGGCCTCCAC | 7011 |
rs534916559 | snp | C/T | 8.32882e-05 | 0.00645269 | intron-variant | TEP1 | GRCh38.p7 | 14:20391101 | TTCAGCGGGGGCTGA[C/T]TGGACAAGTGTCAGG | 7011 |
rs534946326 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367529 | ACCATATTGACTAAA[A/G]TTGAAAGTCGTGTCA | 7011 |
rs534999065 | in-del | -/ACA | 0.00755907 | 0.0610114 | intron-variant | TEP1 | GRCh38.p7 | 14:20368782 | CACACACACACACAC[-/ACA]CACACACACTTACCA | 7011 |
rs535003545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396498 | TTACAGCCCACATGG[A/C]AACAGCTTGAGGGCC | 7011 |
rs535033370 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367981 | AAATGCCCTGATGCA[A/T]GACTGACTTATTCTC | 7011 |
rs535067369 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TEP1 | GRCh38.p7 | 14:20410392 | AGGATCACTTGAGCC[C/T]AGGAGTTTAAAACCA | 7011 |
rs535093385 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20399544 | CCTTTTATTTATTTA[A/T]ATTTATTTTTGGCTG | 7011 |
rs535106984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20404512 | TGCTGAGGAAAGCTG[A/C]GGGGAAACCAAATTG | 7011 |
rs535155752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20393112 | GTCCCAGCTACTCGG[A/G]AGGCTGAAGCAGGAG | 7011 |
rs535336908 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | TEP1 | GRCh38.p7 | 14:20388459 | TTGAGGGAAATGGAT[C/G]GTATCCAGAGGAAAA | 7011 |
rs535374360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380782 | TGAGAGTCACGTGCT[C/T]ACCCTCTTGGCATTT | 7011 |
rs535483591 | snp | A/C | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377398 | CCAGCCCTGCAAGGA[A/C]CCATCTTCTGCACCA | 7011 |
rs535509384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400098 | GCCAAGATTGCGCCA[C/T]TGCATTCCGGCCTGG | 7011 |
rs535550848 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20390002 | TCAGGAAGTTTGTGG[A/G]CAGTTGTTAAAGGTG | 7011 |
rs535582638 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365430 | AGGTGCCTGCCACCA[C/T]GCCCAGCTAATTTTT | 7011 |
rs535609549 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366840 | TCTTCTTTAACCCTC[A/G]GAAAGAAAGGGCCTG | 7011 |
rs535688717 | snp | A/T | 1.64762e-05 | 0.00287016 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372855 | ACCAATGTGGCCTGG[A/T]GCCTGGTGTACACAA | 7011 |
rs535710085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388579 | TAGACATAATTTTCT[A/C]TGGATCAAGAATTGA | 7011 |
rs535831407 | snp | A/C | 3.30868e-05 | 0.00406723 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378059 | TCAGTAACTGGCAAC[A/C]CGCATGCAGGAAAAG | 7011 |
rs535833438 | snp | A/G | 3.30087e-05 | 0.00406242 | intron-variant | TEP1 | GRCh38.p7 | 14:20381425 | ACAGATATTGAGAAA[A/G]GCTCAGCCCTGCATC | 7011 |
rs535954018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411513 | TCTCCTTGTTTTCAC[A/G]ACACCCATATGTCCC | 7011 |
rs535973621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20372221 | TCAACATCTCCATAT[C/G]TTCTGTACATGTTCC | 7011 |
rs536120307 | snp | A/T | 1.66299e-05 | 0.00288352 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395468 | GCCTTGTGTACTCTC[A/T]GCTTCTCCCTCTTGA | 7011 |
rs536223124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392459 | AATCTAAATCTGTTC[A/G]AGGCTTTAGAGCTAA | 7011 |
rs536224724 | snp | A/C | 0.000427934 | 0.0146214 | intron-variant | TEP1 | GRCh38.p7 | 14:20386674 | ATGATTCCCACCCCC[A/C]ATCCATAGACACTGC | 7011 |
rs536244942 | snp | A/C/G | 3.3373e-05 | 0.0040848 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20380233 | TGGGGTCAAGGTCTT[A/C/G]CCTTTGCTGATTTTT | 7011 |
rs536258411 | snp | A/C/T | 4.99275e-05 | 0.00499616 | intron-variant | TEP1 | GRCh38.p7 | 14:20386056 | CTCCCCAGCCCTCCT[A/C/T]CAAACCTGTCTGCCT | 7011 |
rs536292885 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413598 | GCAAGACGACATGCC[A/G]GGGCTGCGACGCGAA | 7011 |
rs536309882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20387030 | ACCTCTGCCTCCAGG[G/T]TTCAAGCAATTCTCC | 7011 |
rs536339887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20408640 | CTAAGAGAGAGGGAT[A/G]GGGAAAAGGTAAGGC | 7011 |
rs536376569 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414401 | CTCCCCAAAATTTAT[A/G]TATTGAAACCCTAAT | 7011 |
rs536448705 | snp | C/T | 0.000930476 | 0.0215493 | intron-variant | TEP1 | GRCh38.p7 | 14:20382103 | CCTCATCTAACCATA[C/T]GGTGTCCCCGCCCCC | 7011 |
rs536496042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402817 | GTATATATTTCATAA[A/T]GTTTTTAACTCACTT | 7011 |
rs536500848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409125 | TCCTCTTAGGTAACC[A/T]AGGAACTTTTTCTTA | 7011 |
rs536545444 | snp | A/G | 1.64795e-05 | 0.00287045 | intron-variant | TEP1 | GRCh38.p7 | 14:20382572 | GAGACAAAGCAGCTG[A/G]AGAGAGAATGGGAAG | 7011 |
rs536566223 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20378618 | CAGGAGCAACCTTGT[C/T]CAGTTACCCTGCCCT | 7011 |
rs536628354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388815 | GTTGCTGCTATGCCT[A/G]GATGGCTGTAAAAGA | 7011 |
rs536689558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20398591 | TTACACGTAACACAT[A/G]ACACTGTATCATATG | 7011 |
rs536715398 | snp | A/G | 8.24219e-05 | 0.00641905 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383490 | TTCTCACACTCACCC[A/G]GGGAAGCTTCTTTGG | 7011 |
rs536975637 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20379193 | ACCCAAAAAGAAGGC[C/T]AAGGCACAAAGGCCA | 7011 |
rs537243325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20378679 | TCAGCAGCCTCTGCC[A/G]CACTGAGAGAACAAA | 7011 |
rs537255870 | snp | A/C | 1.90029e-05 | 0.00308239 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383876 | AGACTAATGATGCCA[A/C]CTTGGCCCCATCAGG | 7011 |
rs537348800 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20385425 | TCACCCAGGCTGGAG[C/T]GCAATGGCGCAATCT | 7011 |
rs537369164 | snp | C/T | 1.64901e-05 | 0.00287137 | intron-variant | TEP1 | GRCh38.p7 | 14:20372960 | CGCCCAGTAAATACA[C/T]AGCCAGGGTAGAATT | 7011 |
rs537395690 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367448 | TCTCAATTAGTTTTA[A/G]TCTTTGTGAATTTCA | 7011 |
rs537487696 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20409827 | AGATCGAGACCATCC[C/T]GGCTAACACAGTGAA | 7011 |
rs537531057 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20404124 | CTTAGGGAGGCCAAG[A/G]CCAGTGGATCACCTG | 7011 |
rs537540187 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20378921 | CTCATTTCCTTCTCC[C/T]GGGGCTTCCAAAAAA | 7011 |
rs537618990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20390553 | GGGTAGGGGGTTGTA[A/G]CCAGTAGAGCTGATC | 7011 |
rs537682286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20390088 | AAACAAATGTGGCTG[A/G]GCATGTTGACACACA | 7011 |
rs537713175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20385337 | CCTGTAATGTATTGA[A/G]TATTCTGTTACAGAC | 7011 |
rs537718468 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20387569 | AAAAAAAAAGAAATT[A/C]AGCAACTAAGCCAGA | 7011 |
rs537738892 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403159 | GCATAACTTCATCTC[-/A]AAAAAAAAAAAAAAA | 7011 |
rs537801378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20369975 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGTTCACT | 7011 |
rs537855076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20382505 | AGGCGAGGTATGAGG[C/T]GAGGATAGGGAGTGG | 7011 |
rs537863733 | snp | A/G | 3.29511e-05 | 0.00405887 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369554 | TAGGATCCCATCAGA[A/G]CTGGCACACAAAAAT | 7011 |
rs537894543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20398827 | TGCTCCCTTTGTAAA[A/G]GGGATGTAAGTCTTA | 7011 |
rs537977621 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20377222 | CTCTGTCTTAAAAAA[A/C]AAAAAAAGAAAAGAA | 7011 |
rs538005986 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365555 | GCTGGGATTATAGGC[A/G]TGAGCCACCGTGCCT | 7011 |
rs538009064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20372022 | ACCTTTAGTATCTCT[C/T]TACTACCATCCATCT | 7011 |
rs538079794 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392667 | TATACCTTGTTTAGA[A/T]CTTGATTTGAATAAA | 7011 |
rs538103139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20404950 | CCTCCATACTCTATC[C/G]CTTACTCAACTTTCC | 7011 |
rs538164859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400214 | TTTATTCTACTCCAC[C/T]CCAAGTGGTTTCAAC | 7011 |
rs538221458 | snp | C/G | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403446 | AAATGGAGGCTCCAT[C/G]CCCTGTAGGGACAGG | 7011 |
rs538229334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20382876 | ACCATCCCTCTCCTA[C/T]GCTGCTCTGCCCAGC | 7011 |
rs538242871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20379632 | CATGGCTATGTTTTG[A/G]TTCCTTTTTTACCTC | 7011 |
rs538276959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20370765 | GGTAGCAGGTCAGGA[C/T]TTAATAACCTTCCCA | 7011 |
rs538328372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411022 | AGACAGGGTTTCACC[A/G]TGTTCATCAGGATGG | 7011 |
rs538378038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380138 | TCTGTGCCTGGATCC[C/T]TCTCCAGTGTTTCTG | 7011 |
rs538408498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374755 | AGTATAATGATAATG[C/T]ACCTATCTGATATGG | 7011 |
rs538502459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400638 | ATACAATATGAGGTT[C/T]TGTACAGATTCCAAT | 7011 |
rs538526038 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402729 | CTATGCTCTTAAATG[C/G]TACGTACAATACCTT | 7011 |
rs538533062 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397010 | AATTCACATACAATC[C/T]ACCCTACTCAAAATG | 7011 |
rs538564654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20408510 | CTGGCTGCACTGAGC[A/G]TGTATTTGCATGAGA | 7011 |
rs538703678 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20399720 | ATATGATTAAAAAAA[A/G]GAAACACTAGCCACC | 7011 |
rs538845567 | in-del | -/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374090 | CATTTTCTTTTTCTC[-/T]TTTTTTTTTTTTTTA | 7011 |
rs538953011 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375336 | TAATTTTGTATCTTT[A/G]GTAGAGACAGGGTTT | 7011 |
rs539038032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20400588 | TTTTTTTCTGTATCA[A/G]TGTGGGCAAATTACC | 7011 |
rs539047017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20393982 | ATCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 7011 |
rs539086722 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | TEP1 | GRCh38.p7 | 14:20387031 | CCTCTGCCTCCAGGG[G/T]TCAAGCAATTCTCCC | 7011 |
rs539089748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386269 | TAGGCACAAACAGGG[A/T]GACGGGGCCCTGACT | 7011 |
rs539187566 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 14:20416145 | TTCTTCTGAAGGCCA[A/G]CTTTATAAGGCCTCT | 7011 |
rs539278767 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367224 | AAAAATTAGCTGGGC[A/G]TGGTGGTGGGCACCT | 7011 |
rs539302333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409453 | TTCCTGGACCTAGAT[C/G]TCCCTTCTGAGCTTC | 7011 |
rs539336147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411568 | TGTCTTTCTTCCCAA[C/T]AGACCATTAAGTTCC | 7011 |
rs539351442 | snp | A/G | 0.000148794 | 0.00862407 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382046 | TCAGCACTCCGTGCA[A/G]CTGGTCCACAGTCAA | 7011 |
rs539398432 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366294 | TCAGAGCATGGAAGA[A/G]AGACAAATAGAGCTT | 7011 |
rs539474326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20372291 | CAGAAAACTCCTACT[C/T]ATTCTGTAAGTGTCC | 7011 |
rs539531765 | snp | A/C | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367373 | ATCTCAAAAACAAAA[A/C]AAAAAAAAAAAGGTT | 7011 |
rs539628620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388665 | TTCTTCTTTCCTACT[A/G]GATATAATACAAACT | 7011 |
rs539723352 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20409857 | AACCCCATCTCTACT[-/AA]AAAAATACAAAAAAT | 7011 |
rs539777398 | snp | A/G | 1.64795e-05 | 0.00287045 | intron-variant | TEP1 | GRCh38.p7 | 14:20372895 | TTCAGTGCTTCTGAT[A/G]AGCCAGGATGCACCA | 7011 |
rs539812738 | snp | G/T | | | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395938 | AAACTGCCGACTGTG[G/T]ATCACCGACTTCTAG | 7011 |
rs539866708 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20378609 | CCAGACCTCCAGGAG[A/C]AACCTTGTCCAGTTA | 7011 |
rs539903860 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20412324 | AATAAGGACAGTTTA[C/T]TTGAGCAACATAGTG | 7011 |
rs539909441 | snp | A/G | 1.66757e-05 | 0.00288749 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401134 | AGAGCTGTAGGTTGG[A/G]GGGGTATCTGAGGAT | 7011 |
rs539926260 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392699 | CTGTGAAATGATATT[C/T]TTAAACAATTGGAAA | 7011 |
rs539951477 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372069 | TTCTCTTTATAAAAT[C/T]CAGATAATTATTCCA | 7011 |
rs540082135 | snp | C/T | 6.59593e-05 | 0.00574241 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395519 | ATCCTCATTGCCATC[C/T]GAAGCTGCTGACGGC | 7011 |
rs540094945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20390073 | AATAAGTTATATTTA[A/C]AACAAATGTGGCTGG | 7011 |
rs540119345 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20394037 | GGTTGCAGTGAGCTG[G/T]GATTGTGCCATTGCA | 7011 |
rs540221424 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415404 | CAGTGTGTATTAAAA[C/T]TACGCATAAAATGCC | 7011 |
rs540272477 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20408728 | ATCCCAACACTTTGG[A/G]AGCTGAGGCAAGAGG | 7011 |
rs540333340 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20370790 | TTCCCAATAACAAGC[A/G]GCTCCCAGGAAACTG | 7011 |
rs540334115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402858 | ACTGACATGTCACCC[A/G]GCAGTAAAGTACAAT | 7011 |
rs540342712 | snp | A/C/G | 5.80101e-05 | 0.00538537 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396698 | GGTTGCACAGGTTCC[A/C/G]AAGCATGGCCATGAA | 7011 |
rs540405386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20391880 | TCTCCCTCCCTCAAG[C/T]ACCATACCCGCTTCC | 7011 |
rs540527311 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392801 | ACATTCTCATTGTAT[A/T]AAAAATGTCCCTTTT | 7011 |
rs540530248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20398966 | GCACAATCTTGGCTC[C/G]CTGCAACCTCCACTT | 7011 |
rs540587691 | in-del | -/AGA | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20396953 | CAGAGCAAGAAGTTC[-/AGA]AACCAGGCATGTGGA | 7011 |
rs540634960 | snp | A/G | 0.000100296 | 0.00708081 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383569 | CCCATCGATGATCAG[A/G]ACCTGGGTCTGGCCA | 7011 |
rs540803141 | snp | A/C | 6.61726e-05 | 0.00575169 | intron-variant | TEP1 | GRCh38.p7 | 14:20378722 | AGTCATGGCTCAGGG[A/C]CACTCTGACCACTGC | 7011 |
rs540869074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20406614 | ACCTTCAGAGCCTTC[A/G]CCCACATGCTTCATG | 7011 |
rs540891616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401688 | CCTATGTGGTAATTT[A/C]TTTCTTCAAAATAGA | 7011 |
rs540930225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20401233 | GTTTACAGGGCATGT[C/T]TGCCCAAATATGCCT | 7011 |
rs541043353 | snp | A/C | | | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371497 | ATCTTACCAGATTTC[A/C]GATGGAGCATCCCCT | 7011 |
rs541052330 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TEP1 | GRCh38.p7 | 14:20390153 | GAGAATCACTTGAGC[C/T]CAGGAGTTTTAGTTG | 7011 |
rs541113729 | snp | C/G/T | 1.69089e-05 | 0.0029076 | intron-variant | TEP1 | GRCh38.p7 | 14:20395999 | GGAGCCGGGAGTATG[C/G/T]GGGGCTTCAGGGGTC | 7011 |
rs541139530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411730 | ATTTTCAGAGTGTCT[A/G]TGAAGCCCATTTATG | 7011 |
rs541196862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20397504 | ACAAAGCAAGACTCT[A/G]TCTCCAAAAAAAAAA | 7011 |
rs541376820 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413727 | GCTTCCCCCTCTACC[A/G]AATTCGTCTCCTCTG | 7011 |
rs541393321 | snp | C/G | 3.431e-05 | 0.00414172 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374463 | ACAGCACTCTGATGA[C/G]CCAGGAACTGACCAA | 7011 |
rs541460328 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20389459 | GGGGTACAGAGTTAG[A/G]CTAAAGTATCCACCT | 7011 |
rs541513243 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20385609 | AACTCCTGACCTCAG[A/G]TGATCCACCCGCCTT | 7011 |
rs541631809 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367814 | CAGGGTTTCACTATG[C/T]TAGCCAGGATGGTCT | 7011 |
rs541656715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20379840 | TGAATTAATCAGAGT[C/G]ATAACAGGTGTGTTT | 7011 |
rs541669097 | snp | C/T | 0.000148587 | 0.00861809 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382256 | AGGGCAGTCAAGGCC[C/T]GGGGAAGGACATCAG | 7011 |
rs541791972 | snp | G/T | | | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386485 | AGTGACGCCCCAGCG[G/T]AGGTCGATTCCGTGA | 7011 |
rs541814245 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365204 | ATGAAGGACTAATTG[C/T]TCCTTTGTCTTTCTT | 7011 |
rs541859551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20398843 | GGGATGTAAGTCTTA[C/T]TTGAATTATAGCTGG | 7011 |
rs541873167 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20384374 | CCATGCCTCTGGTCA[C/T]CAGTGCTTCTGCTGA | 7011 |
rs541949056 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20365669 | AAAGCACACAAAATA[A/C]AAGCCTCCATTTTTA | 7011 |
rs541960893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20399981 | AGCCAATATGGTGAA[A/G]CGCCGTCTCTACTAA | 7011 |
rs542004202 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20388331 | GGCCGGGGCAACGGG[G/T]TAGGGAAAGGTGTAA | 7011 |
rs542092282 | snp | A/C/T | 8.75137e-05 | 0.00661442 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383278 | GCCCCAAGGCCAGCA[A/C/T]GTGGGCACCCTGGCT | 7011 |
rs542121853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20410642 | AGACAGGGTTCCACT[A/G]TGCTGGCCAGGCTGG | 7011 |
rs542162794 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20409953 | CGTGAACCAGGGAGG[C/T]GGAGCTTGCAGTGAG | 7011 |
rs542208396 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367737 | CCTCAGCCTCCCAAG[C/T]AGCTGGGACTACAGG | 7011 |
rs542221929 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant | TEP1 | GRCh38.p7 | 14:20373605 | AGACACAGAGACTGA[A/G]TCAGAAGAAGGGACG | 7011 |
rs542282942 | snp | C/G | 0.000167224 | 0.00914243 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404728 | GGCCAAGATGTTATT[C/G]GCCACATTCCGGACG | 7011 |
rs542340471 | snp | A/G | 1.65529e-05 | 0.00287683 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368387 | TACCAGTGTCTTCAG[A/G]CTTTGCATCTCTAGC | 7011 |
rs542346254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20405091 | TCATTGATTAAACCT[C/G]CCATTTTCCAAAGCA | 7011 |
rs542463402 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20391225 | TAAAATCCCAAGTTA[A/G]GAGGGGTCAGCTTCA | 7011 |
rs542465299 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20385617 | ACCTCAGGTGATCCA[C/T]CCGCCTTGGTCTCCC | 7011 |
rs542576560 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20404215 | TAAAAATTAGCCAGG[C/T]GTGGTGGCGCACGCC | 7011 |
rs542651992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386334 | TTAGTATCCAAGGAG[C/T]GACTCCCGCCTTCAC | 7011 |
rs542683787 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20407451 | GTTTAAGCAATTCTC[A/G]TGCCTCAGCCTCCCA | 7011 |
rs542690507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20408926 | CCCCTGACCCCCGCT[A/G]CAGGACTATCAGTTT | 7011 |
rs542707501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401911 | AGGGAAAATCAGCTC[A/C]GATTTAAATCACTAA | 7011 |
rs542769602 | in-del | -/A | 3.41828e-05 | 0.00413403 | intron-variant | TEP1 | GRCh38.p7 | 14:20368786 | CACACACACACACAC[-/A]CACACACTTACCAGC | 7011 |
rs542812842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20376861 | AACAAAATCGCACAT[A/G]TGTATTTTCATACAC | 7011 |
rs542850281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409616 | CCCCCTTTGCCCACT[A/G]GAGTTGGAAGTGAGA | 7011 |
rs542876828 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20404086 | GGGCAGGGTGGCTCA[C/T]CTTTACGCCTGTAAT | 7011 |
rs542914214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20398255 | TGGTGGTGGTCGCCT[A/G]TAATCTCAGCTAATC | 7011 |
rs543048819 | snp | A/G | 1.65663e-05 | 0.002878 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380442 | GCAACGTCAGCCTCG[A/G]GGAGCTTTTGTTCCT | 7011 |
rs543052661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388297 | CCTGCTGTGCGTGGT[A/G]ATCACAAACTTGCTG | 7011 |
rs543090080 | snp | G/T | 0.000741137 | 0.0192359 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382670 | CGGTGACCAAGCGCA[G/T]GTAGAGCGGCCGGCC | 7011 |
rs543111775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411237 | CACCTCCCAGCATCA[C/T]CTCTCACTAACACCC | 7011 |
rs543173186 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TEP1 | GRCh38.p7 | 14:20411695 | CAGAAAAAAAAAAAG[A/T]ATATACTGTTTTGTG | 7011 |
rs543214750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20405258 | TACTTACTAAACAAA[C/G]CAAGTCTAGTATACT | 7011 |
rs543245970 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403018 | AAAAATTAGCCAAGC[A/G]TGGTGGCACACGCCT | 7011 |
rs543386164 | snp | C/T | 3.70535e-05 | 0.00430411 | intron-variant | TEP1 | GRCh38.p7 | 14:20383141 | CTCCCAGATTCACCC[C/T]ACACACCCACCGGCC | 7011 |
rs543500689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20401205 | ATAACTCAGAAAAGG[A/G]AAGGTGAGTCATGTT | 7011 |
rs543611237 | in-del | -/AAC | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20383036 | CACAATTTTCTTATT[-/AAC]AACTTCCCATGGACA | 7011 |
rs543676751 | snp | A/T | 0.00018131 | 0.00951957 | intron-variant | TEP1 | GRCh38.p7 | 14:20373169 | GAGAAAGGACGTGTT[A/T]CATTAGGAGCTGGGA | 7011 |
rs543682291 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406596 | ACCACCTTGCTCTAC[C/T]CAACCTTCAGAGCCT | 7011 |
rs543706766 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400392 | TGAGTTTGAGACCAG[C/T]CTGGGCAACATTACA | 7011 |
rs543718388 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20403961 | CGAGATCACTTCATG[A/G]AGATACACGAGAGCA | 7011 |
rs543725269 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20405754 | CATGGTGGCTCACAT[C/T]TGTAATCCCAGCACT | 7011 |
rs543764967 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366512 | ATTTCGAGGCTTGGC[A/C]TGAGGCACATAAGAG | 7011 |
rs543914037 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20380851 | ACCCACACCCCTGCC[C/T]CAACCCTGAGCAGGG | 7011 |
rs543946733 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388943 | TCACAAGGTCAGGAG[G/T]TCAAGACCAGCCTGA | 7011 |
rs544065551 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20375694 | AAAGGACGAGGTGGG[G/T]AGTGTTGTCTTGCCC | 7011 |
rs544121783 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386909 | TAAGCACTATCATTA[A/T]CTCCATTTTAGCAAT | 7011 |
rs544201321 | snp | A/G | 6.92701e-05 | 0.00588475 | intron-variant | TEP1 | GRCh38.p7 | 14:20376285 | TTGGAAAAAGAGAGA[A/G]GGAACAGCTTCCTGA | 7011 |
rs544285147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20399110 | GTTGCTCAGGCTGGT[C/T]TCAAACTCCTGAGCT | 7011 |
rs544339864 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20398118 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 7011 |
rs544341456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20391505 | TCAGTCTGAGTGTTT[A/G]CCTGGGAAAACCAGC | 7011 |
rs544401934 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20404224 | GCCAGGCGTGGTGGC[G/T]CACGCCTGTAATCCC | 7011 |
rs544464079 | snp | C/T | 3.3123e-05 | 0.00406945 | intron-variant | TEP1 | GRCh38.p7 | 14:20382177 | GGAACCAATGTAATC[C/T]GAACCCTGGCCCTCA | 7011 |
rs544515943 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20416055 | GAAAGAAAGGGTTAC[A/G]TGAGGTGACTACAGT | 7011 |
rs544579496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409915 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 7011 |
rs544677091 | snp | A/G | 9.91916e-05 | 0.00704173 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404696 | TGGGGGCGACACGCC[A/G]GCAAGAAAGCAGCAA | 7011 |
rs544739210 | snp | A/C/G | 0.000230667 | 0.010737 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373527 | GTGGATGCCATAACC[A/C/G]TGTGGCCCCATCTAG | 7011 |
rs544742663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20410514 | TGCAACCTCCGCCTC[A/C]CAGGTTCAATCCATT | 7011 |
rs544761724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20407313 | TTAAGCTGGCTCACC[G/T]GAACAGAGGCTTCCT | 7011 |
rs544795498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20413012 | ACATTTAAGCACAGT[A/C]TGGGTTTCTATTATC | 7011 |
rs544837903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20399932 | TTTGGGAGGCCGAGG[C/T]GAGTGGATTACTGGA | 7011 |
rs544897623 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367696 | TCACTGCAAGCTCCG[C/T]CTCCTGGGTTCACGC | 7011 |
rs544918726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396073 | CTTAGACAAGAGATA[C/T]AGAAAAGGGGTAATA | 7011 |
rs545095980 | snp | C/G | | | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365486 | CACCATATTGGCCAG[C/G]CTCGCCTCGAACTCC | 7011 |
rs545097525 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413902 | GGAACTCCTTAAAAG[A/G]AGACGGAAAGCGGAA | 7011 |
rs545400168 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20408920 | CCAACCCCCCTGACC[C/G]CCGCTGCAGGACTAT | 7011 |
rs545428529 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20391279 | GTGGAGGGAGGAAAA[A/G]AGGAGCCAGGATCCC | 7011 |
rs545484986 | snp | A/G | 0.00028005 | 0.0118299 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380374 | GCTGGGGCAGGAGCC[A/G]GGGGTACTGGCTGAG | 7011 |
rs545534570 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20405668 | ACTAACTTACAAAGT[-/C]CAAGGACAGAGAGAA | 7011 |
rs545607613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374985 | AATCTCAGCTACTCA[A/G]GAGGCTGAGGCAGGA | 7011 |
rs545765379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20387724 | CTCAGTAGAGAAAGG[A/T]AGGGCTTGCTCACAA | 7011 |
rs545839521 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366410 | CTGCAGGATTTCTGG[A/C]AAGGATTATGGATCA | 7011 |
rs545892921 | in-del | -/TGACCTCAC | | | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366122 | ATAACAATTATACCA[-/TGACCTCAC]TGTCCTTCTCCAAGA | 7011 |
rs546015654 | snp | C/T | 3.29734e-05 | 0.00406025 | intron-variant | TEP1 | GRCh38.p7 | 14:20377557 | GGGCAGGGGCTGCGC[C/T]CTTTCTAAAGGCTCA | 7011 |
rs546062311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20389367 | CACTGCCCACTAACA[C/T]CCCAAGATGAAAACC | 7011 |
rs546099962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411186 | TCTTGCTCCCCTCTG[C/T]ATCTTCAGCATCATA | 7011 |
rs546204055 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20365736 | ACACAGTTTCTAAAT[G/T]GTTACTCTCAACTTC | 7011 |
rs546213045 | snp | C/T | 5.46264e-05 | 0.00522592 | intron-variant | TEP1 | GRCh38.p7 | 14:20377262 | AATTTGTTAACCCTG[C/T]CCACTGTCTAGTAGT | 7011 |
rs546217485 | in-del | -/C | 9.63948e-05 | 0.00694177 | intron-variant | TEP1 | GRCh38.p7 | 14:20386669 | TAGGGATGATTCCCA[-/C]CCCCCATCCATAGAC | 7011 |
rs546227059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402432 | ACCAACTGAGAAAGC[A/G]TTTTTTCTTATAACG | 7011 |
rs546264155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400427 | CCTTGTCTCTAAAAT[G/T]TAAAAAGAAAAGTAA | 7011 |
rs546311500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396198 | TCTGGGCAGGGTGTG[A/G]TAGCTCACGCCTGTA | 7011 |
rs546347468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411395 | ACCACCCCTCCTTTA[C/T]AAGGCCAAATGCTAC | 7011 |
rs546371878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380534 | CCATTAGCCCCAGCA[C/T]CAAATAAAACCATAT | 7011 |
rs546408828 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409446 | AGATCTATTCCTGGA[C/T]CTAGATCTCCCTTCT | 7011 |
rs546420207 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20388874 | AGTAACTGGAGCCGG[C/G]TGCGGTGGCTCACGC | 7011 |
rs546435212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380132 | TGTGCTTCTGTGCCT[C/G]GATCCCTCTCCAGTG | 7011 |
rs546437049 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20385828 | AGTACCCAGATCTAT[C/G]TGATGGCAACACCTA | 7011 |
rs546547452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402694 | GGAAGATTCAAAGCC[A/G]GGTGACGTGAATCCA | 7011 |
rs546571352 | snp | A/G | 0.000303428 | 0.0123135 | intron-variant | TEP1 | GRCh38.p7 | 14:20408474 | TATGCCTAGAAGGAG[A/G]GAAAGACAGGAGATG | 7011 |
rs546611985 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414125 | CTTAGGTTAATAATC[C/T]TAGCTTCATAAAGAG | 7011 |
rs546631029 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20390861 | TGTGTATTGTCTGTG[C/T]CTTTACCAAATATCT | 7011 |
rs546708939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403112 | TAGTGAGCCAAGACC[A/G]TGCCACTGCAGCTCT | 7011 |
rs547031310 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411317 | CTTATTAATTGCCAA[A/C/G]GTATCTCTTGACTAC | 7011 |
rs547205213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20383427 | AGGCCTCTCTCCTCC[A/G]TGCCGTATCCCTCCT | 7011 |
rs547230883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400854 | CAATGGCAGACCTTA[C/T]AAATCAAATACAACA | 7011 |
rs547231186 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20386995 | GCTAGAGTAAAATGG[C/T]GCGATCTCGGCTCAC | 7011 |
rs547395151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395277 | CATGATCTCTCTTTA[A/G]GACAATGTTAAAGAC | 7011 |
rs547410807 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365435 | CCTGCCACCATGCCC[A/C]GCTAATTTTTTGTAT | 7011 |
rs547448679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400561 | AACTTGATCCTCCTC[C/T]ATTTGACTTTTTTTT | 7011 |
rs547468391 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366594 | GAAACCAGGGCATTG[C/G]ATAGAAATAAAGTCC | 7011 |
rs547547039 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366143 | CACTGTCCTTCTCCA[A/G]GATGAAACAAAAAAC | 7011 |
rs547563378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20406716 | GATATTAGTAAGATG[C/T]TTTGGGGGTCAGAAG | 7011 |
rs547615581 | in-del | -/AA | 0.399432 | 0.200425 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367368 | CTCTATCTCAAAAAC[-/AA]AAAAAAAAAAAAAAA | 7011 |
rs547863529 | snp | C/T | 1.64803e-05 | 0.00287052 | intron-variant | TEP1 | GRCh38.p7 | 14:20381291 | ACTTTGGGAAAGGTG[C/T]CTATGGGGTCTAGGA | 7011 |
rs547931329 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398862 | AATTATAGCTGGAAG[C/G]TTTCAGCCCTCTGGA | 7011 |
rs547961147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20407583 | TGGACTCAAGTGATC[C/T]GCCCGCCTTGGCCTC | 7011 |
rs548063431 | snp | A/G | 1.66735e-05 | 0.00288729 | intron-variant | TEP1 | GRCh38.p7 | 14:20395834 | TGTGGGAGGCAAAGA[A/G]GAGTTGGAAGAAAGG | 7011 |
rs548102163 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367800 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACTATGTT | 7011 |
rs548111919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20370310 | GTAGAGCATTTCCAT[C/T]ACCTCAGAAAATTGC | 7011 |
rs548117418 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375433 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC | 7011 |
rs548127427 | snp | C/T | 4.94458e-05 | 0.00497197 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401551 | TTGGAGGATTCTTTT[C/T]CTCTGACACTGTATC | 7011 |
rs548184058 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20407435 | ACAATCTCGCCTCCC[A/G]GTTTAAGCAATTCTC | 7011 |
rs548184685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20398718 | TTTTCCTGGACAGAG[A/G]TGCATTCAAACCACT | 7011 |
rs548235408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20387445 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 7011 |
rs548257852 | snp | A/G/T | 0.000116728 | 0.00763889 | synonymous-codon, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386568 | TCAGCAGCAGGTCCC[A/G/T]CTCCCCATGCATGTC | 7011 |
rs548261069 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415466 | AGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 7011 |
rs548297655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409189 | TATTTCACCCCTCAA[C/G]TAGAATATGACATTG | 7011 |
rs548326448 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20392462 | CTAAATCTGTTCGAG[C/G]CTTTAGAGCTAATGC | 7011 |
rs548373439 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375835 | GGATCAAAACAGGGG[C/T]TTTGGGTGTCCTCAC | 7011 |
rs548464025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20410743 | CTGTGCCTGGCGGAC[A/T]CCTTTTTTTTTAAGC | 7011 |
rs548475889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20376544 | CTAACTGTACTCCCA[C/T]AGCAGCTGCTCCAGA | 7011 |
rs548482964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20404256 | GCTACTTGGGAGGCT[A/G]AGGAAGGAGAATCGC | 7011 |
rs548604861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20399328 | TTTCTAGATCATTTT[C/T]GGTAAGAAATTAAGT | 7011 |
rs548630409 | snp | A/T | 6.65369e-05 | 0.0057675 | intron-variant | TEP1 | GRCh38.p7 | 14:20389592 | CTGACACTGGGCAGG[A/T]AGTATAAGCACCCTT | 7011 |
rs548684174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20392947 | ATGTAAGCCGGGCAC[A/G]GTGGCTCACGCCTAT | 7011 |
rs548742700 | snp | A/C/T | 1.64833e-05 | 0.00287078 | missense, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401479 | CCAGCAGGGCTTGAA[A/C/T]GTGCTGGGCAGGCTT | 7011 |
rs548814879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20390322 | TACTATTATCTACAC[A/G]TGCTTATTTACATCT | 7011 |
rs548825552 | snp | A/G | 0.00645987 | 0.0564642 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378985 | GGACCCCTTACCGAC[A/G]ACCATGCTGCAGGTC | 7011 |
rs548828788 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395746 | CTGACCTCTGCCCCC[A/C/G]ACCCCGATACACCCT | 7011 |
rs548838442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20377092 | TGGAGGCGCATGCCT[A/G]TAATCCCAGCTACTC | 7011 |
rs548857983 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20413433 | TTCCCGCAGCAGGAA[A/G]CAGAAACTTCGCTCT | 7011 |
rs548919922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20407634 | GCATGAGCCACCGCA[C/G]CCAGCCAGGACAGGA | 7011 |
rs549033173 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414636 | CTGATCTTGGACTTC[C/G]ATTCTCTAGAACTGT | 7011 |
rs549147449 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20379224 | TGAGTCCTTGGCTCT[C/T]TATGTTCCAAGTCAA | 7011 |
rs549187757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402611 | TATTCCCATTTAATA[C/T]GTGAGAAAACTGAGG | 7011 |
rs549194039 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374346 | TCATTTTGCCTCTGG[A/G]ATTAGATACTCCATG | 7011 |
rs549385459 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20409883 | AAAAATTAGCCAGGC[A/G]GGGTGGCGGGCACCT | 7011 |
rs549394001 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367853 | TGACCTCGTGATCTG[C/T]CCACCTCGGCCTCCC | 7011 |
rs549501228 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20370529 | CATTCATCAGCATGC[A/G]GTATCACATTAATTT | 7011 |
rs549635276 | snp | C/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403273 | ATCACAGCCAAGAAT[C/T]CCCAGGAAGAAAGTA | 7011 |
rs549658106 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20391523 | TGGGAAAACCAGCTC[C/T]GGGAACAGGATACTG | 7011 |
rs549728961 | snp | C/T | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415456 | AATTATGGTCAGGCA[C/T]GGTGGCTCACGCCTG | 7011 |
rs549783870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20370518 | CTGTATTATTCCATT[A/C]ATCAGCATGCAGTAT | 7011 |
rs549831896 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20400481 | AAGAAAGAGCCTGCT[A/C]TAGGTAAAAGTAGAC | 7011 |
rs549869900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20371102 | AGTTGAAGGAGGATA[A/G]GAGGATTTGCAGCCA | 7011 |
rs549921997 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398373 | TCAAAGTGAGACTCC[A/G]CCCAAAAAAAAAAAA | 7011 |
rs549941682 | snp | G/T | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372849 | CAGAGCACCAATGTG[G/T]CCTGGAGCCTGGTGT | 7011 |
rs549986291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400051 | ATCCCAGCTACTCGG[A/G]AGACTGAGGCAGGAG | 7011 |
rs550002503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20372083 | TCCAGATAATTATTC[C/T]ACCCAAAATTCTTAG | 7011 |
rs550027186 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366738 | ATTTCTCCAAGAGAA[A/G]CCTACCAAACCAGGA | 7011 |
rs550061278 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387981 | GGACCCCTGTCTTTC[C/T]TGGGGGTGGTGGAAT | 7011 |
rs550087820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20394746 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTTCT | 7011 |
rs550124038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20393764 | ACCAGCCTGGGTGAC[A/G]AAGTGGGACTTTGTC | 7011 |
rs550201306 | snp | C/G | 1.67077e-05 | 0.00289026 | intron-variant | TEP1 | GRCh38.p7 | 14:20378005 | CTCACAACCCACCAC[C/G]AGCCCTCTGCAAGCT | 7011 |
rs550224469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388534 | ACAGATAAAAAAAAC[A/G]TGAAAAGATTTCTGT | 7011 |
rs550280804 | snp | A/G | 4.94303e-05 | 0.00497119 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373531 | ATGCCATAACCGTGT[A/G]GCCCCATCTAGCCCG | 7011 |
rs550336416 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20377071 | AAATATAAAATTAGC[A/C]GGGCGTGGAGGCGCA | 7011 |
rs550348416 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TEP1 | GRCh38.p7 | 14:20411932 | AGCCTGGGCAACATA[A/G]TGAGACCTCTATTTA | 7011 |
rs550355208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380600 | CTCTGGCCCTATATC[A/G]GGAATATCTCTTAAA | 7011 |
rs550405107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374768 | TGTACCTATCTGATA[C/T]GGTGGTTGTGGGGCT | 7011 |
rs550425444 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20369255 | CCTCATTATCTGCCC[A/G]CCTAGGCCTCCCAAA | 7011 |
rs550426965 | snp | C/T | 6.58935e-05 | 0.00573955 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401016 | ACCGACGCTTTGTTC[C/T]CCCGTAGGCTCAGCT | 7011 |
rs550452961 | snp | C/T | 1.65466e-05 | 0.00287628 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383546 | TTCTGGTCCACTAAC[C/T]TATCAGCCCCATCGA | 7011 |
rs550464682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20406118 | GTGAGAAATAAGAGC[C/T]AGGTTGTATCCCTAC | 7011 |
rs550471974 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20406783 | CTTGGGCTGCTTAAC[C/T]TCTCTGAACCTCAGC | 7011 |
rs550478589 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397075 | GCCCAAAGTTTGGAA[C/T]AAAATTTATGCAACA | 7011 |
rs550600450 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403394 | TTCTCTGCTCTTCTC[C/T]GAGAAACCCTATGTA | 7011 |
rs550768497 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414857 | AGGGTTTTGCTATGT[C/T]GCCCAGGCTCTCTAC | 7011 |
rs550789786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392909 | CAAAAGAAAAGAAAA[A/T]GAAAAAAAGATCAGT | 7011 |
rs550851528 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20416420 | AAGGCCAGCAAGGCT[G/T]GTACACTGGAACTAC | 7011 |
rs550852154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20409763 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 7011 |
rs550913661 | snp | A/G | 8.23934e-05 | 0.00641794 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403850 | AGACAGGCGGGCAGG[A/G]GCACCAGCTTATTCT | 7011 |
rs550922188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20387004 | AAATGGCGCGATCTC[A/G]GCTCACTGCAACCTC | 7011 |
rs551048870 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20406074 | AAAAGAAAAGGAAAA[G/T]AAAAGAAAAAAGAAA | 7011 |
rs551081304 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411843 | TCTGGCTGGGTGTGG[C/T]GGCTCACACCTGTAA | 7011 |
rs551358408 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366167 | AAAAAACCCTTCAAG[G/T]GGGCCTGGCCAACAA | 7011 |
rs551402719 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20389535 | AAGTGGGAGTGTCCT[A/G]TGCTTTGGCAGGCGT | 7011 |
rs551571343 | snp | C/G | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396650 | TCTGGAGAATGAGCT[C/G]ATGGTGGCGGGAACT | 7011 |
rs551581435 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20407596 | TCCGCCCGCCTTGGC[C/G]TCCCAAAGTGCTGGG | 7011 |
rs551643726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401989 | GAGTTTAAAAACTAA[A/C]AGTAGGCAGGGCGTG | 7011 |
rs551775773 | snp | C/T | 3.29516e-05 | 0.00405891 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373371 | GCACGGACTGGGCCG[C/T]TGTGTCCCAGGAGGG | 7011 |
rs551779639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20379877 | TCTAGGGCTTCAGGG[A/C]AGTCTGCATGGATTT | 7011 |
rs551815410 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367386 | AAAAAAAAAAAAAAG[C/G]TTTTTTACTTAAGAA | 7011 |
rs551838042 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367677 | AGTGCAGTGGTGTCT[C/T]GGCTCACTGCAAGCT | 7011 |
rs551843035 | snp | A/C | 0.000214725 | 0.0103594 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379074 | AAACAAGCAGAGATT[A/C]CATCACAGCCACTCA | 7011 |
rs551856539 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20415622 | TAATCCCAGCTACTT[A/G]GGAGACTGAGGCAGG | 7011 |
rs551887806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20407060 | GAGGGTTCAGATTAG[C/T]CTTGTCCCTCAACCC | 7011 |
rs551958731 | snp | C/T | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20369966 | TCGCCCAGGCTGGAG[C/T]GCAGTGGCGTGATCT | 7011 |
rs552019817 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20409817 | CAAGGTCAGGAGATC[G/T]AGACCATCCTGGCTA | 7011 |
rs552064892 | in-del | -/AA | 3.29565e-05 | 0.00405921 | intron-variant | TEP1 | GRCh38.p7 | 14:20382578 | AGCAGCTGAAGAGAG[-/AA]AATGGGAAGTAGTGA | 7011 |
rs552093089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396803 | ATGCACCTATAATCT[C/G]AGCTACCAAGGAGGC | 7011 |
rs552105330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396417 | TATACTCTACTGTAA[C/T]TTCTCAAAGGATTTA | 7011 |
rs552164162 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388932 | AGGTGGGTGGATCAC[A/G]AGGTCAGGAGTTCAA | 7011 |
rs552179578 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20392990 | TTAGGAGGCCGAGGC[A/G]GGCAGATCACAAGGA | 7011 |
rs552236614 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20387508 | AGTGAGCCGAGATCA[C/T]GCCACTGTACCCCAG | 7011 |
rs552396370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20377166 | GTTGCAGTGAGCCGA[A/G]ACCGTACCACTGCAC | 7011 |
rs552493703 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409063 | TCCTTGCCTCCTATT[C/T]ACTCTTTAACCAACT | 7011 |
rs552518843 | snp | A/C/G | 3.60128e-05 | 0.00424327 | intron-variant | TEP1 | GRCh38.p7 | 14:20404799 | GGTGAGAGGACTAGA[A/C/G]TCTCAGTCACTCCTC | 7011 |
rs552520737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20399408 | AGATTGCAAAATTCA[C/T]TAATTTCATTCCAAA | 7011 |
rs552523470 | snp | A/C | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405476 | AACTCAGGCTCCAGG[A/C]GGGCAAGTTCACGAC | 7011 |
rs552578880 | snp | C/G/T | 0.000101791 | 0.00713352 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384071 | CTGTCCTGACTGCCC[C/G/T]GTCACCAGGCTCAGC | 7011 |
rs552658685 | snp | A/C | 1.65173e-05 | 0.00287374 | intron-variant | TEP1 | GRCh38.p7 | 14:20387882 | CCCTCCCAATTCACA[A/C]AGGCATAGAAACACA | 7011 |
rs552665582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20378741 | TCTGACCACTGCAGA[A/C]CCCAAGTCTTACCTT | 7011 |
rs552720642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20407167 | TGTGTAAAAGTGGAC[A/G]TGTATTTGCACATGC | 7011 |
rs552770900 | snp | A/G | 3.29484e-05 | 0.00405871 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387921 | CTTGCTGGGAAACAG[A/G]AGCCAAGGGGCTTGG | 7011 |
rs552802098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20371963 | GTCAGGCCCACATTA[C/T]GTCTTTCCTAGGCTA | 7011 |
rs552833105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20405380 | AGCTAGTCACCACCC[C/T]GCCACACACCATAAC | 7011 |
rs552871065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411341 | TGACTACGGGCCTGT[A/G]CACAGGCAGATCCCT | 7011 |
rs552899055 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20412952 | GCGTGAACCACCGCG[C/G]CCGGCCTCCACCTCA | 7011 |
rs552965461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20389851 | ACTCTGAGAGGAGTA[A/C]CTCTCCTGAGAGCAC | 7011 |
rs553055657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396967 | CAGAAACCAGGCATG[C/T]GGAAAGTCCAAGATA | 7011 |
rs553081630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20412276 | GACTCAGATTTTTTT[G/T]AAAAGAGATCTCAAG | 7011 |
rs553265902 | snp | A/T | 0.00062782 | 0.0177064 | intron-variant | TEP1 | GRCh38.p7 | 14:20407853 | TGGCTGGAGTCAAGA[A/T]GAGTGCCTGGAGCTA | 7011 |
rs553342514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20374863 | GGGAGGCCGAGGCAG[A/G]TGGATCGCCTGAGGT | 7011 |
rs553439202 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414542 | CTAGCTCTTTTTCCA[C/T]GATATGAGGATACAA | 7011 |
rs553497732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20385467 | AACCTCCGCCTCCTC[A/G]GTTCAAGCAATTCTC | 7011 |
rs553581851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20393843 | TCTCAGCACTTTGGT[A/T]TGGGAGGCCAAGGTG | 7011 |
rs553734875 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20365720 | TACTTTTTAAATTCC[C/G/T]ACACAGTTTCTAAAT | 7011 |
rs553837694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20393166 | AGCTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC | 7011 |
rs553867154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20372240 | TGTACATGTTCCTTC[C/T]TCTTCCTGAAACACT | 7011 |
rs553923395 | snp | A/G | 8.26795e-05 | 0.00642907 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378061 | AGTAACTGGCAACCC[A/G]CATGCAGGAAAAGCG | 7011 |
rs554019335 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397875 | TCTCCTGCCTCAGCC[G/T]CCGAGTAGCTGGGAT | 7011 |
rs554029900 | snp | A/T | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371499 | CTTACCAGATTTCAG[A/T]TGGAGCATCCCCTGG | 7011 |
rs554040674 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20388234 | TAAAATAAATGAGGA[G/T]GCAGAACCACAGGAA | 7011 |
rs554042533 | snp | G/T | 1.64781e-05 | 0.00287033 | intron-variant | TEP1 | GRCh38.p7 | 14:20382584 | CTGAAGAGAGAATGG[G/T]AAGTAGTGATTAGGA | 7011 |
rs554064688 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20383432 | TCTCTCCTCCGTGCC[A/G]TATCCCTCCTTCTCC | 7011 |
rs554140122 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401679 | CATCCGATCCCTATG[G/T]GGTAATTTCTTTCTT | 7011 |
rs554179168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20405101 | AACCTGCCATTTTCC[A/G]AAGCATCATAGAAGA | 7011 |
rs554190077 | in-del | -/AG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408627 | CCAGAGAATATTCTA[-/AG]AGAGAGAGGGATAGG | 7011 |
rs554303482 | snp | A/C/T | 4.94387e-05 | 0.00497165 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406246 | ACCTTCTTTTCCTGA[A/C/T]GGACATGGTCAGTAG | 7011 |
rs554309448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395027 | GTATTTCAAAATACA[A/C]ACACACACAACAAAA | 7011 |
rs554574631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386708 | GATCACCCTTTAGCA[A/C]TGAGCACAAGCCAGG | 7011 |
rs554713534 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20409848 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAAAA | 7011 |
rs554844783 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TEP1 | GRCh38.p7 | 14:20391839 | GCAGACGGGGAGATG[A/G]GAAGTTGCCACTAAG | 7011 |
rs554872733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20410298 | TGACATACTGTATAT[A/G]GATTTGTCTAAAGGA | 7011 |
rs554935028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20370656 | AAGATTCTTGTACCC[A/G]GCTTTGCAGAATGTA | 7011 |
rs554979978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20388819 | CTGCTATGCCTGGAT[A/G]GCTGTAAAAGAGGAG | 7011 |
rs555096132 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20369960 | ACTCTGTCGCCCAGG[C/T]TGGAGTGCAGTGGCG | 7011 |
rs555131745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20370062 | GGGAACACCGGCGTG[C/T]GCCACCACACCCAGC | 7011 |
rs555193519 | snp | A/C | 1.65318e-05 | 0.002875 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376163 | AACTACAGCAGCTCA[A/C]AGGGCCCTCATGTCC | 7011 |
rs555272032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20412892 | CTCAAACTCCTGACC[C/T]CAGGTGATCCCCAAC | 7011 |
rs555321091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20378682 | GCAGCCTCTGCCGCA[A/C]TGAGAGAACAAATTC | 7011 |
rs555429190 | snp | A/C | 0.0429648 | 0.14013 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401662 | AAAGCAGATTGTAAG[A/C]CCATCCGATCCCTAT | 7011 |
rs555429425 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367898 | ACAAGCGTGAGCCAC[C/T]ATGCCCGGCCTCCTC | 7011 |
rs555552369 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TEP1 | GRCh38.p7 | 14:20388887 | GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 7011 |
rs555671758 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366998 | GGCTGGAGTAACAGA[A/G]GAGGAAAGTTAAGCA | 7011 |
rs555700987 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20387487 | AACCCAGGAGGCAGA[A/G]CTTGCAGTGAGCCGA | 7011 |
rs555816062 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20395129 | AGAAAAAGAAAACCA[C/T]GAATCAGAGCAGAAG | 7011 |
rs555827102 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20396457 | AAAACTTATCTCCCT[C/G]AACCTAGCTGTATTC | 7011 |
rs555989745 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20412749 | CTGCAATCTCTGCCT[A/G]CCGAGTTCAAGCGAT | 7011 |
rs556028666 | snp | A/G | 0.00092219 | 0.0214533 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384631 | CTTTCTGTCTGCTTA[A/G]GTAGCTCTTCAGTTC | 7011 |
rs556075397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20404059 | CTTCATTAGAAACAT[A/G]AGGTCCTGGCTGGGC | 7011 |
rs556085095 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366718 | CTAGACCAGGGTGTA[C/G]TGGTATTTCTCCAAG | 7011 |
rs556121735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20370851 | CTCAATCCAAAAAGT[A/G]TTGAACATCTATTAA | 7011 |
rs556126779 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393152 | AACCCAGGAGGTGGA[A/G]CTTGCAGTGAGCCGA | 7011 |
rs556193146 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371493 | TTGGATCTTACCAGA[C/T]TTCAGATGGAGCATC | 7011 |
rs556293733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20392716 | TAAACAATTGGAAAA[C/T]TTGAATATGGACTAA | 7011 |
rs556397357 | snp | G/T | 3.33823e-05 | 0.00408534 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377305 | AGCCAAGAGCTCCTG[G/T]GAAGTGGCCAGTCCT | 7011 |
rs556448529 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20394323 | TTAATACAAAAGTTA[A/T]GAATATTTCACACTC | 7011 |
rs556481932 | snp | G/T | | | | | GRCh38.p7 | 14:20416104 | AGGAAGTGAGGGGAG[G/T]GATTGAAGGAGTCCA | 7011 |
rs556522203 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20387609 | CTATTTGGCAAAGCC[A/C]CAATGAAAAAGCCAG | 7011 |
rs556565199 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20410604 | ATTTTTTTTTCTTTT[G/T]TTTTTTTTGTATTTT | 7011 |
rs556568310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20376934 | GAACAGTGATTTGTG[C/G]GCCAGGCGCAATGGC | 7011 |
rs556593626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374366 | GATACTCCATGCACC[A/G]TCTCCCAAAGCCCCC | 7011 |
rs556651670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380146 | TGGATCCCTCTCCAG[C/T]GTTTCTGGTCATCCT | 7011 |
rs556718875 | snp | C/T | 1.6918e-05 | 0.00290839 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368867 | CACCAGCAACTCAGG[C/T]AGCACATGGAGGGCT | 7011 |
rs556721945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411026 | AGGGTTTCACCATGT[G/T]CATCAGGATGGTCTC | 7011 |
rs556829002 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402201 | TACTCCCAGCTACTC[A/C/G]GGAGGCTGAGGCAGG | 7011 |
rs556837593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20397227 | CAAAAGAGAAATTTC[A/G]TAGTGTAAGTTGATT | 7011 |
rs556924489 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368674 | ATACATTGCAAGTGA[C/T]TGAAGAAAACAGAAT | 7011 |
rs556961423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20413015 | TTTAAGCACAGTCTG[C/G]GTTTCTATTATCACA | 7011 |
rs557069481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409825 | GGAGATCGAGACCAT[C/T]CTGGCTAACACAGTG | 7011 |
rs557070156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20408545 | ATCTTCCCCACAGCC[C/T]TCCTGATAATGCCAA | 7011 |
rs557120421 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20413537 | GAGACTCTCGGGCCC[C/G]GGCGGGGCGCAGCAG | 7011 |
rs557176206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386276 | AAACAGGGAGACGGG[A/G]CCCTGACTCGCAACT | 7011 |
rs557258873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409489 | CACTTATCCATTTCC[C/T]CGTTGGACATCCCCA | 7011 |
rs557326321 | snp | A/C | | | | | GRCh38.p7 | 14:20416510 | TCACCCAGAGTAGGA[A/C]CCAGGCATCAGTAGT | 7011 |
rs557360349 | snp | A/G | 6.59685e-05 | 0.00574281 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403731 | GACTGACTGGAGAGC[A/G]GGGTGGCCGGCGGGG | 7011 |
rs557433204 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20394841 | TACTGATTCAGGAGA[G/T]TCCTAGTTACTGAGC | 7011 |
rs557479628 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409347 | ATGCTCCTTGCAGTT[C/G]TATTCTAATCCTTTT | 7011 |
rs557557501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388756 | GAGTATTTGAGGATC[A/G]TGGAGCAATAAGAGA | 7011 |
rs557640593 | snp | C/T | 0.000164948 | 0.00908003 | intron-variant | TEP1 | GRCh38.p7 | 14:20369642 | ACCCTGGGCCATCTC[C/T]CGGCTCCTCAGGTCC | 7011 |
rs557703766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20375496 | GGCTCAGCTTCATCA[C/T]TGACCTTGGAAATGT | 7011 |
rs557823389 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20383083 | ACAAAGGAGCAGGTC[G/T]GTGCAAGGCAGCTAG | 7011 |
rs557868347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395723 | CAACCCTTGGGGCTG[A/G]CAAGTGCCTGACCTC | 7011 |
rs557877169 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20412142 | AAAGGACAACAATAT[A/C]TCACTGGACGTCAGT | 7011 |
rs558039617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20378637 | TTACCCTGCCCTCAG[A/C]AGGGAAGGCCTTCTC | 7011 |
rs558039664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20372350 | TTTCTCAAATTTTGA[A/C]GCCCCAGGAATATGT | 7011 |
rs558059485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411575 | CTTCCCAATAGACCA[G/T]TAAGTTCCTGAGGAG | 7011 |
rs558143527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20405705 | CGAGATGTGGAGTCC[A/C]GTTGAGAACTTACAA | 7011 |
rs558167424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20390081 | ATATTTAAAACAAAT[A/G]TGGCTGGGCATGTTG | 7011 |
rs558171708 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366489 | GGAAATGATGGTCCA[A/G]AAGGTATATTTCGAG | 7011 |
rs558277823 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20408801 | GTGAAACCTCATCTC[C/T]ACAAAGTTTTAAAAA | 7011 |
rs558308574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20368952 | TCTCAGGGGCCCCTC[C/T]TCAGAGAAGCATCAC | 7011 |
rs558347552 | snp | A/G | 9.88826e-05 | 0.00703076 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395905 | AATGGCATCATGGGC[A/G]TTAAGAAATCTGAAT | 7011 |
rs558432457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20391885 | CTCCCTCAAGCACCA[C/T]ACCCGCTTCCACAGC | 7011 |
rs558626222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20375444 | CAGGTGTGAGCCACC[A/G]TGCCCAGACCTAGGC | 7011 |
rs558678382 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20385455 | TTGGCTCACAGCAAC[C/T]TCCGCCTCCTCGGTT | 7011 |
rs558681616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20403946 | CCCTCCAAAACAAAA[C/T]GAGATCACTTCATGG | 7011 |
rs558683901 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20376458 | GTGTGTACATAGGAC[A/G]GGAACGTGCGGCACT | 7011 |
rs558741190 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405337 | CAGAAATCCTTCCTA[A/G]GAGAAGCTCCTCCCA | 7011 |
rs558818052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392651 | AACCAAATGTAATGT[A/G]TATACCTTGTTTAGA | 7011 |
rs558858344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20399881 | AATTATCTTCATATG[C/G]CTGGGCGTGGTGGCT | 7011 |
rs558976288 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20415901 | TACCCATTTAAATGT[A/G]TAAAATCATCCTAAT | 7011 |
rs559021708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20404859 | TGATTGAGTGTGCCT[A/G]TATAAAACCTTTCCT | 7011 |
rs559070239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20405922 | AGGAGGCTGAGGCAG[A/G]AGAATAATGAATTCA | 7011 |
rs559072711 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20411835 | ACCTATTTTCTGGCT[G/T]GGTGTGGTGGCTCAC | 7011 |
rs559092923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20401236 | TACAGGGCATGTCTG[C/T]CCAAATATGCCTAAA | 7011 |
rs559133860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20406646 | TCTGCCCCTGCTTTC[A/G]TCTCTTCATTGGCGT | 7011 |
rs559198220 | snp | A/G | 3.29462e-05 | 0.00405857 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372751 | AAATTTCCGGGTGCC[A/G]AACCCTTCCGCAGTT | 7011 |
rs559370657 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20407073 | AGCCTTGTCCCTCAA[C/T]CCGAAACACAAGTAT | 7011 |
rs559452795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395335 | GTTCTGAGCCACTGC[A/G]ATGACTGACAAGCAA | 7011 |
rs559538770 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367043 | CAATAGATTCTTCCA[C/T]ATGATTGAATTTTAG | 7011 |
rs559576716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20396021 | TCAGGGGTCCACTCT[A/G]TTAGCTTTGTGGGAA | 7011 |
rs559586479 | snp | C/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402796 | TTTTAAAACTTCCTG[C/T]GAAAGGTATATATTT | 7011 |
rs559665750 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20390224 | ACGGAGTGAGACCCT[A/G]TCTCAAAAAATAAAA | 7011 |
rs559679151 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TEP1 | GRCh38.p7 | 14:20407587 | CTCAAGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 7011 |
rs559808274 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367801 | TTTTTAGTAGAGACA[A/G]GGTTTCACTATGTTA | 7011 |
rs559883972 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413809 | GAAAAGATTTTAGCA[A/T]GCTCGCTGCCTAGCT | 7011 |
rs560009498 | snp | C/T | 5.13562e-05 | 0.0050671 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374481 | AGGAACTGACCAAGC[C/T]GCTGTCCTGACTCTG | 7011 |
rs560086043 | snp | C/T | 1.65419e-05 | 0.00287588 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373785 | TTCAAGGTCCCATCC[C/T]GGCTCACAGACACCA | 7011 |
rs560162440 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365284 | TTTTTTTCTTTTTTT[C/T]TTTTTTTTGACCAAG | 7011 |
rs560208828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20376976 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGTGGGTG | 7011 |
rs560280403 | snp | A/C/G | 6.60462e-05 | 0.00574625 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382259 | GCAGTCAAGGCCTGG[A/C/G]GAAGGACATCAGGCC | 7011 |
rs560330692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20376363 | TGGGGGCTGAGGGTG[A/G]CACCTGAGGCTCAGC | 7011 |
rs560362598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20394543 | GGAGTGCAATGGCGC[A/G]ATCTCAGCTCACAGC | 7011 |
rs560404490 | snp | A/G | 1.6908e-05 | 0.00290753 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383584 | GACCTGGGTCTGGCC[A/G]GGATGCAGGGACTCA | 7011 |
rs560420130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20370356 | CCATCAATACCAGAC[C/T]ATCACCACAAAAGCT | 7011 |
rs560477022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20404282 | ATCGCTTGAACCTGG[A/G]AGGCGGAGGTTGCAG | 7011 |
rs560597767 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367757 | GGGACTACAGGTGCC[C/T]GCCGCCACACCTGGC | 7011 |
rs560600840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400404 | CAGCCTGGGCAACAT[C/T]ACAAAGACCTTGTCT | 7011 |
rs560616674 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20372019 | CTTACCTTTAGTATC[C/T]CTCTACTACCATCCA | 7011 |
rs560677836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20393648 | AATACAAAAATTAGC[A/G]GGGTGTGGTGGTATG | 7011 |
rs560691106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401912 | GGGAAAATCAGCTCC[A/G]ATTTAAATCACTAAG | 7011 |
rs560738605 | in-del | -/T | 0.00359783 | 0.0422607 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413960 | ATCAGTCAATCAAAG[-/T]TCGCTGAACTGAGAG | 7011 |
rs560845586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386388 | ACCATGCCCACCTCA[A/G]GTCCACCACTCAAGC | 7011 |
rs560875045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20407454 | TAAGCAATTCTCGTG[A/C]CTCAGCCTCCCAAAT | 7011 |
rs561063319 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20377013 | CTATGGTCAGGAGTT[C/T]GAGACCAGCATGACC | 7011 |
rs561144867 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413983 | ACTGAGAGCAAGTGC[C/T]TCCCCTCCTGTTGAT | 7011 |
rs561153429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409645 | GACAGACTTTACTTT[G/T]AATCCTCCTTTACCT | 7011 |
rs561153518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403034 | TGGTGGCACACGCCT[A/G]TAGTCCCAGCTATTC | 7011 |
rs561161215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374617 | GTGTAGGGTGGAAGG[A/C]GGTTAGCCACGTAAT | 7011 |
rs561316824 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414648 | TTCCATTCTCTAGAA[C/T]TGTGAGAAATAATAT | 7011 |
rs561326345 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20369148 | GAGTAGCTGGGACTA[C/T]AGGCACCCGCCACCA | 7011 |
rs561351351 | snp | C/T | 8.34885e-05 | 0.00646044 | intron-variant | TEP1 | GRCh38.p7 | 14:20395989 | CATGAGCACAGGAGC[C/T]GGGAGTATGGGGGGC | 7011 |
rs561457093 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20375047 | AGTGAGCAGAGATTG[A/C/T]GCCACTGCACTCCAG | 7011 |
rs561514201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20405786 | TGGGAGACTGAGGTG[A/G]GCAGACCACCTGAGG | 7011 |
rs561606771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392072 | AGATTCAATGGCTAC[A/G]TAGTTTTAAATTGTA | 7011 |
rs561616483 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392022 | GACCCACTAGCTACA[C/G]TTACCACATGAATCC | 7011 |
rs561711049 | snp | C/T | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373557 | GCCCGACGGTTACCA[C/T]CAGAAGCTCTGACCC | 7011 |
rs561724576 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366680 | CAGTGCCCTTTAACT[C/G]CCCAAGTCTTCAAAA | 7011 |
rs561864324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400800 | ATCTATGATGCCAAC[A/G]TTACTCAAAGCAGGT | 7011 |
rs562006408 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367102 | GGCACAATGGCTCAC[A/G]CCTGTAATCCCAGAA | 7011 |
rs562031514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388955 | GAGTTCAAGACCAGC[C/T]TGACCAACATGGTGA | 7011 |
rs562177398 | snp | C/T | 3.29647e-05 | 0.00405971 | intron-variant | TEP1 | GRCh38.p7 | 14:20378902 | CCTGGCCATCAGCTC[C/T]CTCCTCATTTCCTTC | 7011 |
rs562268085 | snp | C/T | 4.94588e-05 | 0.00497262 | intron-variant | TEP1 | GRCh38.p7 | 14:20373227 | ACCCTTGACCTTTTT[C/T]TGTGCCAGTAACACA | 7011 |
rs562368758 | snp | C/T | 4.94376e-05 | 0.00497156 | intron-variant | TEP1 | GRCh38.p7 | 14:20373619 | AGTCAGAAGAAGGGA[C/T]GGAGCAGGGGAGAAA | 7011 |
rs562385164 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TEP1 | GRCh38.p7 | 14:20405968 | AATGAGCTGAGATTA[C/T]GCCATTGCACTCCAA | 7011 |
rs562401024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20376342 | GGCCAAAGACAGGAG[C/T]GGCCATGGGGGCTGA | 7011 |
rs562441180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20398208 | CACGGTGAAACCCCA[C/T]CTCTACTAAAAATAC | 7011 |
rs562441240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20391517 | TTTGCCTGGGAAAAC[C/T]AGCTCTGGGAACAGG | 7011 |
rs562476801 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20369982 | GCAGTGGCGTGATCT[C/T]GGTTCACTGCAACCT | 7011 |
rs562602902 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386910 | AAGCACTATCATTAT[C/G]TCCATTTTAGCAATC | 7011 |
rs562662785 | snp | A/G | 6.61978e-05 | 0.00575278 | intron-variant | TEP1 | GRCh38.p7 | 14:20382178 | GAACCAATGTAATCC[A/G]AACCCTGGCCCTCAG | 7011 |
rs562813389 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20416129 | AGTCCACACAGGGCC[C/T]TTCTTCTGAAGGCCA | 7011 |
rs562815203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20409786 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 7011 |
rs562832702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20399933 | TTGGGAGGCCGAGGC[A/G]AGTGGATTACTGGAG | 7011 |
rs562845388 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402675 | TAGCCAGTAAGGGGT[A/G]GATGGAAGATTCAAA | 7011 |
rs563027562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20399134 | CTGAGCTCAAGTGAT[C/T]TGCCCGCCCCAGCCT | 7011 |
rs563029133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395684 | TTCCCTCATCTTTTC[C/T]TACCAGTAATGTGAC | 7011 |
rs563040138 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392905 | TCTTCAAAAGAAAAG[A/G]AAAAGAAAAAAAGAT | 7011 |
rs563061832 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20365909 | TAGATGGGTAGAAGA[A/C]AAGATTGTTCAAATG | 7011 |
rs563116066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396119 | GTCATCATTTTAGGA[C/T]GTGAGAAAAGGTAAC | 7011 |
rs563133782 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20375318 | TGTGTCACCACGCCT[-/G]GCTAATTTTGTATCT | 7011 |
rs563213330 | snp | C/T | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378184 | ACAGCCACAACCCCC[C/T]CAGGCACATTGAAGG | 7011 |
rs563255789 | snp | G/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367072 | AGAAATATAATAAAG[G/T]TCTTTTATGGGCCGG | 7011 |
rs563265963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20401383 | GTTTGAGAACTACTG[A/G]GATGGGGGCCACGGA | 7011 |
rs563272661 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388915 | AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA | 7011 |
rs563272927 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20412364 | TATCCTTAAAAGGAC[A/G]GTCTCACTATTTTGC | 7011 |
rs563321426 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20377772 | GGAACCAAGAAAAGG[A/G]CTTAAGGATACCACC | 7011 |
rs563433513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20384823 | CCTCAAGTAGAGAGC[G/T]CCTGACTCCAGCACC | 7011 |
rs563541851 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414592 | CCCAAGGAAGACCCT[C/T]ATCTTCAGAGGCAGA | 7011 |
rs563568149 | snp | C/T | 4.98724e-05 | 0.00499337 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379948 | CCAAGTTCTCAGGTC[C/T]AACAGGTAAACTGTC | 7011 |
rs563722546 | in-del | -/AA | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 14:20416585 | TTCATGTTGAAACTC[-/AA]AATCTGCGATGTGAT | 7011 |
rs563731688 | snp | A/G/T | 0.000511634 | 0.0159863 | intron-variant | TEP1 | GRCh38.p7 | 14:20374548 | ATATCTACAGAGTCA[A/G/T]AAGTCAGAGGAGTGG | 7011 |
rs563736779 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TEP1 | GRCh38.p7 | 14:20385564 | TTTTAGTAGAGACAG[A/G]GTTTCACCATGTTGG | 7011 |
rs563792348 | in-del | -/AAG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406077 | AGAAAAGGAAAATAA[-/AAG]AAAAAAGAAAAGGGG | 7011 |
rs563900699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20375011 | CAGGAGAATCATTCG[A/C]ACCTGGGAGGTGGAG | 7011 |
rs563923500 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393782 | GTGGGACTTTGTCTC[A/C]ATTAAAAAAAAAAAA | 7011 |
rs564036189 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20407775 | GAGAAGATAGCCAGA[C/G]ACAGAGCAGCACAGA | 7011 |
rs564091653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20411212 | TCATACACAAAACCC[A/G]ACTTCCGGTCACCTC | 7011 |
rs564115788 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20391913 | AGCCCACTCCATTTC[C/T]GGTGTAGAGGACTGG | 7011 |
rs564158499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20377014 | TATGGTCAGGAGTTC[A/G]AGACCAGCATGACCA | 7011 |
rs564181579 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20365737 | CACAGTTTCTAAATG[G/T]TTACTCTCAACTTCC | 7011 |
rs564360358 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20400433 | CTCTAAAATTTAAAA[A/C]GAAAAGTAATAATTT | 7011 |
rs564424398 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365343 | CAATGATGCGATCTC[A/G]GCTCACTGCAACCTC | 7011 |
rs564431450 | snp | A/C | 1.64738e-05 | 0.00286995 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372827 | AGGTGTGTGCCGAGG[A/C]CCAGATCAGAGCACC | 7011 |
rs564448862 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20400761 | TAAAAACTTGTACAT[A/C]ACCTAACTACATCTG | 7011 |
rs564448905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20394631 | ATTACAGGCACCCAC[C/G]ACCACACCCGGCTAA | 7011 |
rs564608044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395137 | AAAACCATGAATCAG[A/G]GCAGAAGCAGAGAGG | 7011 |
rs564710669 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406537 | TGTTCTCTCCCTTCA[C/T]ACACCAGCACTGATG | 7011 |
rs564800860 | snp | A/G | | | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404725 | AATGGCCAAGATGTT[A/G]TTGGCCACATTCCGG | 7011 |
rs564831665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20375216 | TCACTCTTGTTGCCC[A/C]GGCTGGAGTGCAATG | 7011 |
rs564831685 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20381800 | ACTGGAGCAGCTGGA[A/G]CAGTAGCTCATTCAT | 7011 |
rs564962777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20375686 | TGCCAGAAAAAGGAC[A/G]AGGTGGGGAGTGTTG | 7011 |
rs564969403 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20391339 | GGTGAAAGTGAGACA[G/T]ATTTTGGTGATGCAA | 7011 |
rs564988883 | in-del | -/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413756 | TGGCTAATTTTCGTC[-/T]TTTTTTCTCCCATTA | 7011 |
rs565037889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386789 | TAGTGGTCTCAACTG[C/T]AGGGCCCTGGAATTT | 7011 |
rs565054632 | snp | C/T | 0.000118089 | 0.00768312 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386475 | TCTCCTCCTCAGTGA[C/T]GCCCCAGCGGAGGTC | 7011 |
rs565111644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20398977 | GCTCGCTGCAACCTC[C/T]ACTTTCCAGGCTCAA | 7011 |
rs565168246 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375319 | GTGTCACCACGCCTG[C/G]CTAATTTTGTATCTT | 7011 |
rs565184291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20370209 | GTGAGCCACTACACC[C/T]GGGTAAGTGCACAAA | 7011 |
rs565215525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20393238 | AAAAAGAGAAGAAAA[A/G]AAAGAAAATGTAATA | 7011 |
rs565323339 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TEP1 | GRCh38.p7 | 14:20400107 | GCGCCATTGCATTCC[A/G]GCCTGGGCAAAAAGA | 7011 |
rs565362016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20404827 | CTCCCGTAGCTTTCT[G/T]CCCTGAAATTACTTG | 7011 |
rs565471148 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20369189 | ATTTTTTGTATTTTT[C/T]AGTAGAGATGGGGTT | 7011 |
rs565610296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392808 | CATTGTATAAAAAAT[G/T]TCCCTTTTTAAAGAA | 7011 |
rs565690271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388618 | CACAGTGACATGGCC[A/C]ACTCTTGACAGTGAA | 7011 |
rs565718546 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405128 | AAGATATTTCCCACC[A/G]CGCTCTTCTTTGCTT | 7011 |
rs565795590 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366159 | GATGAAACAAAAAAC[C/G]CTTCAAGTGGGCCTG | 7011 |
rs565932694 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20403589 | ACCATATGCCCATGA[A/G]CTCTACCCAGCTCCC | 7011 |
rs565959359 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415407 | TGTGTATTAAAACTA[C/T]GCATAAAATGCCTTG | 7011 |
rs565975246 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398919 | CTTTTTTTTTTTATT[C/T]TTGAGATGGAGTCTG | 7011 |
rs566004922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20389041 | TAGTCCCAGGTACTC[A/G]GGAGGCGGAGGCAGG | 7011 |
rs566289483 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367348 | AGCCTAGGTGACAGA[A/G]CCAGACTCTATCTCA | 7011 |
rs566406989 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415498 | CTTTGGGAGGCCAAG[G/T]TGGGCAGATTACCTG | 7011 |
rs566463246 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415000 | GAGTCTACGGCCATA[A/C]CACCCCGAACGCGCC | 7011 |
rs566561972 | in-del | -/AGAT | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20395076 | TCAAAAAATACAGAA[-/AGAT]AGAAACAAAAAGAAA | 7011 |
rs566577611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20369936 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 7011 |
rs566607880 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20382456 | GACAGTGTGGAGGAA[C/T]GAAAAAGTAAAGAAC | 7011 |
rs566706267 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20392973 | CCTATAATCCCAACA[A/C]TTTAGGAGGCCGAGG | 7011 |
rs566815089 | in-del | -/TC | | | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365275 | TTGCTTTCTTTTTTT[-/TC]TTTTTTTTTTTTTTT | 7011 |
rs566818873 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367703 | AAGCTCCGCCTCCTG[C/G]GTTCACGCCATTCTC | 7011 |
rs566872419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392476 | GGCTTTAGAGCTAAT[A/G]CCCAGTGAACAAAAA | 7011 |
rs566995895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20400702 | AGTTACAGAGATATC[A/G]ATATGAGTACAATGA | 7011 |
rs567012780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20410758 | TCCTTTTTTTTTAAG[A/C]ATGTTTGCTTATTAG | 7011 |
rs567057228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20377116 | GCTACTCGGGAGGCC[A/G]AGACAGGAGAATTGC | 7011 |
rs567093592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20384848 | AGCACCAAGGCTGAC[A/G]TGGGGCTGCAAAGGC | 7011 |
rs567155649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20370665 | GTACCCGGCTTTGCA[C/G]AATGTATGTACTCCT | 7011 |
rs567168578 | snp | A/G | 1.69384e-05 | 0.00291014 | intron-variant | TEP1 | GRCh38.p7 | 14:20395446 | CCAGACAGTGCATAC[A/G]TACCTGGCCTTGTGT | 7011 |
rs567209139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395752 | TCTGCCCCCCACCCC[A/G]ATACACCCTGAGACT | 7011 |
rs567315209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20379246 | CCAAGTCAAGCACAC[A/G]TTCAAGTGGGGGCCT | 7011 |
rs567343304 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20407693 | CCAATGTAGATATGC[A/G]ATAAAAGTAATGATG | 7011 |
rs567373899 | in-del | -/AA | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20412601 | CACAAACAGGATCAT[-/AA]AAGTTAGATGCTATT | 7011 |
rs567450326 | snp | C/T | 1.64841e-05 | 0.00287085 | intron-variant | TEP1 | GRCh38.p7 | 14:20373459 | AACAGAAGGTTATTC[C/T]GCATACCTTCCCCAC | 7011 |
rs567465613 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402612 | ATTCCCATTTAATAC[C/G]TGAGAAAACTGAGGC | 7011 |
rs567548730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374132 | TCACTCTGTTACACT[A/G]GAGGCTGGAGTGCAG | 7011 |
rs567699830 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367906 | GAGCCACCATGCCCG[A/G]CCTCCTCTGGGTAGT | 7011 |
rs567701110 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20410727 | TTACAGGTGTGAGCC[A/T]CTGTGCCTGGCGGAC | 7011 |
rs567739264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20410266 | CCACCTTTGTTGAAA[C/T]CCTCTAATCCATGTG | 7011 |
rs567865042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20396921 | AAATGAGGGATGATT[A/G]GAGAGAGGTCAGAGA | 7011 |
rs567907501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20391533 | AGCTCTGGGAACAGG[A/T]TACTGCTCAGGATCC | 7011 |
rs567940650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380746 | AATCTCTGGTCCAAG[A/G]GATCAAGGTGAAAGG | 7011 |
rs568003857 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386159 | CCCCACAAACAGCTG[C/T]GCGTTCTCCACCTCC | 7011 |
rs568031425 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20404498 | TGTCTGGGCACCAAT[G/T]CTGAGGAAAGCTGAG | 7011 |
rs568168457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400090 | TGCAGTGAGCCAAGA[C/T]TGCGCCATTGCATTC | 7011 |
rs568168956 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TEP1 | GRCh38.p7 | 14:20409803 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 7011 |
rs568409336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20394747 | GATCCACCTGCCTCG[G/T]CCTCCCAAAGTTCTG | 7011 |
rs568469698 | snp | A/T | 1.65578e-05 | 0.00287726 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378052 | CCAGCCGTCAGTAAC[A/T]GGCAACCCGCATGCA | 7011 |
rs568528349 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TEP1 | GRCh38.p7 | 14:20379680 | ACAAAACTGACCACT[C/T]GGTGGGCAATGACAA | 7011 |
rs568535639 | snp | A/G | 1.66183e-05 | 0.00288251 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378527 | CTGCCCACGGACTGT[A/G]TCCCACAGCTGAGGG | 7011 |
rs568691596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411952 | ACCTCTATTTAAAAA[A/G]AAAAAGGAATGTATT | 7011 |
rs568710933 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367126 | CCCAGAACTTTAAGA[A/G]GCTGAGGTGTGCAGA | 7011 |
rs568743500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20375314 | GGCATGTGTCACCAC[A/G]CCTGGCTAATTTTGT | 7011 |
rs568831208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20369271 | CCTAGGCCTCCCAAA[A/G]TGCTGGGATTATAGG | 7011 |
rs568859443 | snp | G/T | 1.74476e-05 | 0.00295356 | intron-variant | TEP1 | GRCh38.p7 | 14:20381085 | TAGGGATATGAAGGG[G/T]CTGGTGAGAAGGGAC | 7011 |
rs568926149 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414370 | ACACTCCCTGCAATG[A/G]TCTTTATGTTTGTGT | 7011 |
rs568945732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380604 | GGCCCTATATCAGGA[A/G]TATCTCTTAAAAGTA | 7011 |
rs568992106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20387022 | TCACTGCAACCTCTG[C/T]CTCCAGGGTTCAAGC | 7011 |
rs569055758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392419 | AAATAGTATATATAT[A/G]GGATCACCTATGAAC | 7011 |
rs569079461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20387440 | GCCTGTAGTCCCAGC[C/T]ACTCGGGAGGCTGAG | 7011 |
rs569090363 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414881 | TCTCTACCTCCAGGG[C/T]TCAAATAGTCCTCCT | 7011 |
rs569090450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20408566 | ATAATGCCAATGATT[C/T]GTGGGTAGAAAACAA | 7011 |
rs569174414 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403402 | TCTTCTCTGAGAAAC[C/T]CTATGTACCTTGGAA | 7011 |
rs569244251 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20415780 | TAAAACAAGTTTTCA[A/G]CTACATGAATGACTG | 7011 |
rs569274619 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20409884 | AAAATTAGCCAGGCA[A/G/T]GGTGGCGGGCACCTG | 7011 |
rs569313598 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20400603 | ATGTGGGCAAATTAC[C/G]TAAAACTTCCATGTC | 7011 |
rs569403945 | snp | C/G | 1.67259e-05 | 0.00289183 | intron-variant | TEP1 | GRCh38.p7 | 14:20382086 | CTCAAGCTCTCTGAG[C/G]CCCTCATCTAACCAT | 7011 |
rs569458985 | snp | C/T | 0.000345286 | 0.0131348 | intron-variant | TEP1 | GRCh38.p7 | 14:20395418 | GGTAGCCCCGATTGC[C/T]CACCCTTGGCTCCCA | 7011 |
rs569617290 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TEP1 | GRCh38.p7 | 14:20387682 | GCCATGATGTCTGCC[A/G]TCATCTTTGCATTCT | 7011 |
rs569636217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20389070 | GGAGGATCGCTTGAA[C/T]CCAGGAGATGGAGGT | 7011 |
rs569661974 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366672 | GTAAAACTCAGTGCC[C/T]TTTAACTCCCCAAGT | 7011 |
rs569695599 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20413407 | CTGGGTGCCTGACCT[A/G]GGGCGTCCGATTCCC | 7011 |
rs569825555 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20407530 | ATTTTTGGTAGAGAC[A/G]GGGTTTCACCATGTT | 7011 |
rs569931978 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20379158 | CCCTTGACCCTCCAA[G/T]TCCCACCACTCCAGG | 7011 |
rs569977211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20378678 | GTCAGCAGCCTCTGC[C/T]GCACTGAGAGAACAA | 7011 |
rs570073177 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367408 | ACTTAAGAAAATCAG[A/G]GTTCATGGCTATGAT | 7011 |
rs570092902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401638 | ATGACCATGGGAACT[C/T]TCTTCAATAAAGCAG | 7011 |
rs570098132 | snp | C/G | 0.000411912 | 0.0143453 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373397 | GAGGGTGTGGGTTTG[C/G]CACACCTAGGAGGAA | 7011 |
rs570123995 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367844 | TTGATCTCCTGACCT[C/T]GTGATCTGCCCACCT | 7011 |
rs570184375 | snp | C/T | 0.000403843 | 0.0142042 | intron-variant | TEP1 | GRCh38.p7 | 14:20373847 | AGAGCAGAGTCATAT[C/T]GAGCAGGACATGGGA | 7011 |
rs570223072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396427 | TGTAACTTCTCAAAG[C/G]ATTTACTGAACCCCA | 7011 |
rs570236390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20385304 | AACAAGGCACTAATA[A/G]CTAACATTCATTGAA | 7011 |
rs570355394 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20407720 | GATGCCAGTGAAGAT[A/G]GTCCTGCAACAAAAG | 7011 |
rs570428304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20375999 | AGATCTATACTAGAT[C/T]TGGCAAAACAAAAAG | 7011 |
rs570491882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20410080 | TCACAGAGTTGTTAT[A/T]GAAATAAATGAGAAA | 7011 |
rs570525354 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20385374 | TTTTTTTTTATTTTT[C/T]ATTTTTTGTTTTTTT | 7011 |
rs570531511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20369974 | GCTGGAGTGCAGTGG[C/T]GTGATCTCGGTTCAC | 7011 |
rs570556557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20404400 | AGAATAAGACCATTT[G/T]TTTTTCTCAAACTTT | 7011 |
rs570566176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20403959 | AACGAGATCACTTCA[C/T]GGAGATACACGAGAG | 7011 |
rs570624956 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388950 | GTCAGGAGTTCAAGA[C/T]CAGCCTGACCAACAT | 7011 |
rs570672845 | in-del | -/AAAAAAAAAAAAAAAAAA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410039 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAAA]TGCCTACCTCACAGA | 7011 |
rs570676486 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20380859 | CCCTGCCCCAACCCT[C/G]AGCAGGGCCCCCATA | 7011 |
rs570682271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20398783 | TTGTGCACCAGCCCA[C/T]ACCATCAGCAGCTTC | 7011 |
rs570712065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20387547 | ACACAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 7011 |
rs570744790 | snp | A/C | 5.02239e-05 | 0.00501093 | intron-variant | TEP1 | GRCh38.p7 | 14:20377994 | TGCTACTCCTCCTCA[A/C]AACCCACCACCAGCC | 7011 |
rs570785981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400044 | GCCTGTAATCCCAGC[C/T]ACTCGGGAGACTGAG | 7011 |
rs570861761 | snp | A/G | 9.88484e-05 | 0.00702954 | intron-variant | TEP1 | GRCh38.p7 | 14:20384529 | GGCAAATCAAGCACA[A/G]CCAGGTCAGAGCAGG | 7011 |
rs570866202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20382839 | GCAGACGCCAGGTCC[A/G]TGGCATCATCCCAGG | 7011 |
rs570921974 | snp | A/C | 1.73066e-05 | 0.0029416 | intron-variant | TEP1 | GRCh38.p7 | 14:20383402 | AAAGAAAAGGAGAAC[A/C]ACATTGGAGAGGCCT | 7011 |
rs570937555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411344 | CTACGGGCCTGTGCA[C/G]AGGCAGATCCCTGGA | 7011 |
rs570964029 | snp | C/T | 8.23961e-05 | 0.00641804 | intron-variant | TEP1 | GRCh38.p7 | 14:20384353 | CAGACCACCCCATGT[C/T]CCTCTCCATGCCTCT | 7011 |
rs570986448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380136 | CTTCTGTGCCTGGAT[C/G]CCTCTCCAGTGTTTC | 7011 |
rs571042520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20410994 | ACCCAGCTAATTTTT[A/G]TATTTGTAGTAGAGA | 7011 |
rs571076482 | in-del | -/T | 5.06423e-05 | 0.00503176 | intron-variant | TEP1 | GRCh38.p7 | 14:20384944 | CTGGCCTGTCTGGCC[-/T]TTTGGGGAAGGAGCC | 7011 |
rs571214437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374743 | AACTATTTAATGAGT[A/G]TAATGATAATGTACC | 7011 |
rs571269554 | snp | C/T | 0.000164723 | 0.00907383 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403388 | TCACCTTTCTCTGCT[C/T]TTCTCTGAGAAACCC | 7011 |
rs571293260 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20382169 | ACCCCAAGGGAACCA[A/G]TGTAATCCGAACCCT | 7011 |
rs571309207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402700 | TTCAAAGCCGGGTGA[C/T]GTGAATCCAGATTCT | 7011 |
rs571321793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374296 | ATGGGGGGTCTTCCT[A/G]TGTTGCCTAATCTCT | 7011 |
rs571366052 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20413496 | GGAGGAGCCGGATGC[A/G]GATCTGAGAAGAGAC | 7011 |
rs571397343 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414293 | TTGAGGGCATTCTGT[C/T]CTCTATTAACTGAGC | 7011 |
rs571454435 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368049 | CATGCTCTGTTCAAA[C/T]TGAATGTTGGCCAAC | 7011 |
rs571457393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20397690 | AGAATTTCACCACTG[A/G]CCTCTGTCACTTCCT | 7011 |
rs571552429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20408966 | TTAGTAGAGAGGCCT[C/T]GCAATATAATCTGGA | 7011 |
rs571559930 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415017 | ACCCCGAACGCGCCC[A/G]ATCTCCTCTGATCTT | 7011 |
rs571733253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20399856 | AGGAAGTGGAGATGG[A/G]TGCATATAGAATTAT | 7011 |
rs571936039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20393183 | GATTGTGCCACTGCA[C/G]TCCAGCCTGGGCGAC | 7011 |
rs571948833 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20375459 | GTGCCCAGACCTAGG[C/T]TTTCTTATTAGAGAG | 7011 |
rs572021538 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20381765 | CAGTGGGCTCCTATT[-/C]CCCCCCTCAAATAGC | 7011 |
rs572180917 | snp | C/T | 3.62595e-05 | 0.00425775 | intron-variant | TEP1 | GRCh38.p7 | 14:20396612 | TGGCTACCAGCCCCT[C/T]ACACATACCGCATGC | 7011 |
rs572221058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20382991 | AGGCCATTCACCGGG[G/T]GAAGAGGGCTGGGTG | 7011 |
rs572222933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20376982 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCAC | 7011 |
rs572227783 | snp | C/T | 0.000135423 | 0.0082276 | intron-variant | TEP1 | GRCh38.p7 | 14:20371637 | TCAGGTGAAGACTAG[C/T]TCAAAAAAGTACATG | 7011 |
rs572255011 | snp | A/C | 0.000191473 | 0.00978262 | intron-variant | TEP1 | GRCh38.p7 | 14:20380499 | GGGTGGCAGAATGTC[A/C]CTGGGGAGCCAGCTG | 7011 |
rs572295170 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20399986 | ATATGGTGAAACGCC[A/G]TCTCTACTAAAAATA | 7011 |
rs572385365 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401708 | TTCAAAATAGATTTG[A/G]CCAAGGAGCAGGAAT | 7011 |
rs572419968 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20411558 | ATCACCTGTTTGTCT[G/T]TCTTCCCAATAGACC | 7011 |
rs572447720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20400416 | CATTACAAAGACCTT[A/G]TCTCTAAAATTTAAA | 7011 |
rs572507962 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366393 | TGCCATGCCATAGTT[C/T]GCTGCAGGATTTCTG | 7011 |
rs572509474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20388872 | GAAGTAACTGGAGCC[A/G]GGTGCGGTGGCTCAC | 7011 |
rs572533608 | snp | G/T | | | | | GRCh38.p7 | 14:20416522 | GGACCCAGGCATCAG[G/T]AGTTTTTGAAGTTTC | 7011 |
rs572566810 | in-del | -/T | 0.170408 | 0.236992 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365277 | GCTTTCTTTTTTTTC[-/T]TTTTTTTTTTTTTTT | 7011 |
rs572566843 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397942 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 7011 |
rs572576924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395037 | ATACACACACACACA[A/G]CAAAAACAAAAAAGA | 7011 |
rs572689091 | snp | C/T | | | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384065 | CTTGCCCTGTCCTGA[C/T]TGCCCCGTCACCAGG | 7011 |
rs572714377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374809 | ACATAAAGGACTTAG[G/T]CTGGGCACGGTGGCT | 7011 |
rs572725085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20389356 | TGGAACACAGTCACT[A/G]CCCACTAACATCCCA | 7011 |
rs572785758 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414445 | TATTTAGGGTGGGAT[C/T]TCTGGGAGGTCATTA | 7011 |
rs572791359 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20413392 | CTGGGGCTGGAAACC[C/T]TGGGTGCCTGACCTG | 7011 |
rs572851093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20381761 | GCACACAGTGGGCTC[C/T]TATTCCCCCCTCAAA | 7011 |
rs572876770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20408706 | GGTGCAGTGGCTCAT[A/G]CCTGTAATCCCAACA | 7011 |
rs572952959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409690 | GATAAGATACTTAAA[G/T]TCTCTGTGTCTCTAG | 7011 |
rs572984577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20391327 | GGGATGTAGTGAGGT[G/T]AAAGTGAGACATATT | 7011 |
rs573039767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20382106 | CATCTAACCATACGG[C/T]GTCCCCGCCCCCACC | 7011 |
rs573082103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20391859 | TTGCCACTAAGTATT[C/G]AGTCTTCTCCCTCCC | 7011 |
rs573163551 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20398955 | GTCACTCAGTGGCAC[A/T]ATCTTGGCTCGCTGC | 7011 |
rs573209107 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20415841 | TGTCACTCATTGTGT[A/G]GTAGTGTCCTAAACA | 7011 |
rs573412334 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20390426 | GCATCATGTCGATAG[C/T]TTGAAATCAGCCACG | 7011 |
rs573497478 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388542 | AAAAAACGTGAAAAG[A/G]TTTCTGTAATTTTAG | 7011 |
rs573505192 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408722 | CCTGTAATCCCAACA[C/G]TTTGGGAGCTGAGGC | 7011 |
rs573537136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20412195 | TGGCTTCTGTGCCCA[A/G]TACACTTTGCTCATG | 7011 |
rs573596366 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409891 | GCCAGGCAGGGTGGC[A/G]GGCACCTGTAGTCCC | 7011 |
rs573697445 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378217 | AAGGTACGGATAGAG[A/G]CTCCGGGTGCCCCCA | 7011 |
rs573721101 | in-del | -/C | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366158 | AGATGAAACAAAAAA[-/C]CCTTCAAGTGGGCCT | 7011 |
rs573813782 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20401230 | CATGTTTACAGGGCA[G/T]GTCTGCCCAAATATG | 7011 |
rs574100077 | in-del | -/CTC | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20411499 | GATTTAGGTGGCCTT[-/CTC]CTTGTTTTCACAACA | 7011 |
rs574106872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20379803 | CAAGCCCTTTGAGCT[A/G]ATGTGCAGGCAGTAA | 7011 |
rs574240373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20385458 | GCTCACAGCAACCTC[C/T]GCCTCCTCGGTTCAA | 7011 |
rs574247700 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413670 | TTTGTTATTGTTTCT[A/G]TTTTTTTTCCCTTTC | 7011 |
rs574302906 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384647 | GTAGCTCTTCAGTTC[C/T]GAGATCCGACGTGCG | 7011 |
rs574318903 | snp | C/T | 6.59294e-05 | 0.00574111 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380274 | GGTTTATTAAGCCAT[C/T]GTAGTGTGTGTTGGA | 7011 |
rs574344613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20410907 | GCTCACTGCAACCTC[A/G]ACTTCCCGGGTTCAA | 7011 |
rs574369490 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20404067 | GAAACATGAGGTCCT[A/G]GCTGGGCAGGGTGGC | 7011 |
rs574457737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20370857 | CCAAAAAGTGTTGAA[C/T]ATCTATTAAGTAACT | 7011 |
rs574530381 | snp | A/G | 0.000181619 | 0.00952766 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382247 | GTGACTTCTAGGGCA[A/G]TCAAGGCCTGGGGAA | 7011 |
rs574607213 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20386252 | CATGGTATCAGGGAA[C/T]ATAGGCACAAACAGG | 7011 |
rs574615904 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20392746 | AATAACAGATGATTT[C/T]ACCGAGGAATTATTT | 7011 |
rs574685634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20382550 | GCAAAGGACGTGGGA[C/T]AGGGATGAGACAAAG | 7011 |
rs574701502 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20387214 | GCTGGGATTACAGGC[A/G]TGAGCCACGGCGCTC | 7011 |
rs574703579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20393110 | CAGTCCCAGCTACTC[A/G]GGAGGCTGAAGCAGG | 7011 |
rs574754148 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404630 | TAAAGCTCAGCCACC[C/T]GGATCCAGTCAGAAG | 7011 |
rs574821042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388328 | TTGGGCCGGGGCAAC[A/G]GGGTAGGGAAAGGTG | 7011 |
rs574897319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20370072 | GCGTGCGCCACCACA[C/T]CCAGCTGATTTTTTT | 7011 |
rs574944869 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20405038 | CTTTGGAAGACCTCC[A/T]GCATCAACAGCTATC | 7011 |
rs574955538 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TEP1 | GRCh38.p7 | 14:20400326 | TGCAGTGGCTCATGC[C/T]TATAATTCCAGCACT | 7011 |
rs574960107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400701 | GAGTTACAGAGATAT[C/T]GATATGAGTACAATG | 7011 |
rs574994014 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368367 | ATTTTATAATTATTA[A/G]AAGCTACCAGTGTCT | 7011 |
rs575125803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20407410 | GTTGCCCAGATTGGA[A/G]TGCAGTGACACAATC | 7011 |
rs575188747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20397260 | TGAAGTATATACTAA[C/T]ATAATGTAGCACATT | 7011 |
rs575255815 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20391207 | AGGGAATAAGAAAAA[C/G]TGTAAAATCCCAAGT | 7011 |
rs575281141 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388307 | GTGGTAATCACAAAC[G/T]TGCTGTTGGGCCGGG | 7011 |
rs575305560 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414608 | ATCTTCAGAGGCAGA[C/G]CATGCTGGCAATCTG | 7011 |
rs575307190 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413553 | GGCGGGGCGCAGCAG[C/G]TGCTGGAAGGGCAGC | 7011 |
rs575415949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402303 | ACAGAGCAAGACTTC[A/G]TCTCAAAAATAAATA | 7011 |
rs575493037 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TEP1 | GRCh38.p7 | 14:20409836 | CCATCCTGGCTAACA[C/T]AGTGAAACCCCATCT | 7011 |
rs575552658 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386290 | GGCCCTGACTCGCAA[A/C]TGAGTAAAGAAAAGG | 7011 |
rs575633199 | snp | A/C/T | 3.29757e-05 | 0.00406041 | splice-donor-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381551 | ACTTGGGCTGCAATC[A/C/T]CCTGCAATGAGGATG | 7011 |
rs575793302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20375020 | CATTCGAACCTGGGA[G/T]GTGGAGATTGCAGTG | 7011 |
rs575825210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411631 | CAATTGCTGGTCAGC[A/G]GGATTCAGAGGCTTT | 7011 |
rs575853436 | snp | A/G/T | 3.29501e-05 | 0.00405884 | intron-variant, missense, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403747 | GGGTGGCCGGCGGGG[A/G/T]TGTCTCTTGGCCCGG | 7011 |
rs575854405 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409499 | TTTCCCCGTTGGACA[A/T]CCCCACTGGATGACT | 7011 |
rs575880559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20375508 | TCATTGACCTTGGAA[A/G]TGTTCTGAGTTCAAT | 7011 |
rs575905823 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20388293 | CCCTCCTGCTGTGCG[A/T]GGTAATCACAAACTT | 7011 |
rs575922915 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366790 | CACTTATCTCCTACA[A/G]GTCCTTGAATTCTTG | 7011 |
rs576018081 | snp | G/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369678 | TTACCACTCACCAGA[G/T]TCAGGTTTGGCTTGA | 7011 |
rs576101722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20383105 | GGCAGCTAGCGGCCT[C/T]GGCACCCCAGGTCCT | 7011 |
rs576135483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388758 | GTATTTGAGGATCAT[A/G]GAGCAATAAGAGAGA | 7011 |
rs576212325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20405723 | TGAGAACTTACAAAA[C/G]GGGATTAGGGCCAGG | 7011 |
rs576252574 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366506 | AGGTATATTTCGAGG[C/T]TTGGCATGAGGCACA | 7011 |
rs576278403 | snp | C/T | 0.000379422 | 0.0137683 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378163 | ACCATACTGTCCAGC[C/T]GGCCCACAGCCACAA | 7011 |
rs576376917 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400771 | TACATCACCTAACTA[A/C/T]ATCTGGTATAATGAT | 7011 |
rs576402003 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406400 | AATCAAACCAACGAC[C/T]CTGGGGTAGTAGTGG | 7011 |
rs576416008 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366950 | GTTGTCTGTCTCCCA[C/T]GCTCTGAAAATTCTA | 7011 |
rs576548393 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372946 | TATGCAACCTCTAAC[A/G]CCCAGTAAATACACA | 7011 |
rs576669885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20390087 | AAAACAAATGTGGCT[A/G]GGCATGTTGACACAC | 7011 |
rs576731233 | snp | C/G | 0.000924092 | 0.0214754 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395944 | CCGACTGTGGATCAC[C/G]GACTTCTAGAAAGCA | 7011 |
rs576741171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20403615 | CTCCCCTGCATTTCT[C/G]TGACTCCCTTTGCTC | 7011 |
rs576795921 | snp | A/G | 1.66715e-05 | 0.00288712 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376244 | GCAGCTGCCTTGGCC[A/G]CAGCTGCACTGTGAA | 7011 |
rs576930509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402954 | ACGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 7011 |
rs577005761 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20385557 | TTTGTATTTTTAGTA[A/G]AGACAGGGTTTCACC | 7011 |
rs577049654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20382136 | CACACCCAGTCTCTC[C/T]TTGAACTGCCTGCTG | 7011 |
rs577071482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392656 | AATGTAATGTGTATA[A/C]CTTGTTTAGATCTTG | 7011 |
rs577160541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409914 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 7011 |
rs577171319 | snp | C/G | 0.000399281 | 0.0141238 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20378753 | AGACCCCAAGTCTTA[C/G]CTTTAGGCATCCTCC | 7011 |
rs577256556 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398967 | CACAATCTTGGCTCG[C/T]TGCAACCTCCACTTT | 7011 |
rs577274597 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20370240 | TCTTAAATGTACATC[A/G]GCGATGTATTTTTAC | 7011 |
rs577348155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20404886 | TCCTGAGCCCTCCAC[A/G]TTGTCCACAAAATAC | 7011 |
rs577381645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404684 | TATCGTCGCAGGTGG[A/G]GGCGACACGCCGGCA | 7011 |
rs577393684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401823 | CAAGCAGTTAACATG[A/G]GTTGACTGGCTTGTG | 7011 |
rs577486837 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365554 | TGCTGGGATTATAGG[C/T]GTGAGCCACCGTGCC | 7011 |
rs577549878 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20379366 | ATGGGGTTACATGGG[A/G]TAGGGGATGACATGA | 7011 |
rs577554312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20412293 | AAAGAGATCTCAAGC[C/T]AAAAATAAACAGAAA | 7011 |
rs577612849 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376411 | GGGAGTCACAAGGCT[A/G]TGGAGAGGCCCTGGG | 7011 |
rs577617123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20412982 | ACTCTTCAAGTGGCT[A/G]TATGGTAGTCTAGCA | 7011 |
rs577618442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20406659 | TCATCTCTTCATTGG[C/T]GTCACAACCTGGGAG | 7011 |
rs577647442 | snp | C/T | 4.94344e-05 | 0.00497139 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373520 | ACCAAGAGTGGATGC[C/T]ATAACCGTGTGGCCC | 7011 |
rs577783499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20407295 | GACTCTGCTATAGTA[A/G]CATTAAGCTGGCTCA | 7011 |
rs577824299 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20399793 | ACATTAAAAGAATAA[A/G]TTTACATGTCCTTAC | 7011 |
rs577930460 | snp | G/T | 1.64825e-05 | 0.00287071 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390738 | AGTATTCAGGGACCA[G/T]CCATCATTTTCATCA | 7011 |
rs577976422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20390225 | CGGAGTGAGACCCTG[A/T]CTCAAAAAATAAAAA | 7011 |
rs578023496 | snp | A/C | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386185 | CCTCCCCAAGGCACA[A/C]TTCCAGTTGTCTGTA | 7011 |
rs578084121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20385472 | CCGCCTCCTCGGTTC[A/C]AGCAATTCTCCTGCC | 7011 |
rs578132843 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413848 | CTCCTTCCTAATATC[A/G]AAGACGGTCAGACTC | 7011 |
rs578156152 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20395647 | ATGATGACAGGTAAA[C/T]TTCCGAGTTAGGCAG | 7011 |
rs578196223 | snp | C/T | 0.000233723 | 0.0108077 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374518 | AGAGCCCCACAGAGC[C/T]ATCACTGGAGCAGGA | 7011 |
rs578197522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380836 | TCTTTTTTCCCTGAC[A/C]CCCACACCCCTGCCC | 7011 |
rs578236632 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366089 | ACTTTTACCTAGAAG[C/G]TGTTCTTGACTTTAC | 7011 |
rs578252250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374934 | ATCTCTACTAAAAAT[A/G]CAAAAAATTAGCTGG | 7011 |
rs745308885 | snp | C/T | 1.64931e-05 | 0.00287163 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378803 | AGCCGGCAGTCTGGG[C/T]TCAGGCAGCAGCCAG | 7011 |
rs745328441 | snp | C/T | 1.7161e-05 | 0.0029292 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382340 | GTGGCAGGCAGGGTC[C/T]GGAGTCTCTCAGACA | 7011 |
rs745360903 | snp | A/C | 1.65548e-05 | 0.002877 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401123 | ACTTCGAGAAAAGAG[A/C]TGTAGGTTGGAGGGG | 7011 |
rs745369528 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | TEP1 | GRCh38.p7 | 14:20384280 | TGCCATGCTCCTCAG[C/T]ACTCCCAGGCTAAAA | 7011 |
rs745374474 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369687 | ACCAGATTCAGGTTT[A/G]GCTTGAGTTATCGAT | 7011 |
rs745400494 | in-del | -/T | 9.90508e-05 | 0.00703673 | intron-variant | TEP1 | GRCh38.p7 | 14:20373222 | AGGCCACCCTTGACC[-/T]TTTTTTGTGCCAGTA | 7011 |
rs745435784 | snp | G/T | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384460 | AAACTCCTCCAGCCC[G/T]CCAACATAGGGCCGG | 7011 |
rs745454302 | snp | C/T | 3.30398e-05 | 0.00406434 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395489 | TCCCTCTTGAGCTGC[C/T]CATACAACACAGGTA | 7011 |
rs745456716 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400796 | AATGATCTATGATGC[C/T]AACATTACTCAAAGC | 7011 |
rs745457205 | snp | C/G | 1.65252e-05 | 0.00287443 | intron-variant | TEP1 | GRCh38.p7 | 14:20389310 | GACCTGGCAAAGGAA[C/G]AAGCAGTCATTAACC | 7011 |
rs745504936 | snp | C/T | 3.31384e-05 | 0.00407039 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406399 | GAATCAAACCAACGA[C/T]CCTGGGGTAGTAGTG | 7011 |
rs745530291 | snp | A/G | 4.9498e-05 | 0.00497459 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381960 | GCCCATGGGGTAGGG[A/G]TCTCCACTGTTACCA | 7011 |
rs745542073 | snp | C/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401646 | GGGAACTTTCTTCAA[C/T]AAAGCAGATTGTAAG | 7011 |
rs745556287 | snp | A/C | 1.76493e-05 | 0.00297058 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407875 | CTGGAGCTATTACCA[A/C]AGTTGCTTCCTGAGC | 7011 |
rs745570250 | snp | C/T | 1.64982e-05 | 0.00287208 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373725 | CTAATGGGTCCTGAG[C/T]GAGCAGGGATGCTGG | 7011 |
rs745582124 | in-del | -/GG | 1.64728e-05 | 0.00286987 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369438 | TCCCTGCAGGTAGAT[-/GG]GTCTGTCCCTGGAGT | 7011 |
rs745601560 | snp | C/G | 2.61025e-05 | 0.00361256 | intron-variant | TEP1 | GRCh38.p7 | 14:20374576 | TGGGATTATCAGCAT[C/G]CCTCCAGCATTTTGG | 7011 |
rs745635981 | snp | A/C | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390756 | ATCATTTTCATCAAA[A/C]TCCTGAAGGAAAGAG | 7011 |
rs745639320 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408223 | CCAAGGAGAGGATGT[C/T]TGGGTGGGCAGACAC | 7011 |
rs745665744 | snp | A/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408311 | CTTCAAGGAGAGGAT[A/T]TCTGAGTGGGTAGAT | 7011 |
rs745678289 | in-del | -/G | 4.94177e-05 | 0.00497055 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408183 | ATGGTCTTCAGGTCA[-/G]AAAGTGTGGCCAGGC | 7011 |
rs745693278 | snp | C/G | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368498 | GCAAGCTGCAGGGTG[C/G]AGTTAGCGCCCAGCC | 7011 |
rs745704966 | snp | A/G | 1.74114e-05 | 0.00295049 | intron-variant | TEP1 | GRCh38.p7 | 14:20386415 | AAGCCCCTCATCCCC[A/G]ACCCAGCCCCTCTTC | 7011 |
rs745719303 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20404943 | TCTAAGTCCTCCATA[C/G]TCTATCCCTTACTCA | 7011 |
rs745735597 | snp | A/G | 1.65132e-05 | 0.00287339 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382260 | CAGTCAAGGCCTGGG[A/G]AAGGACATCAGGCCC | 7011 |
rs745737029 | snp | A/G | 5.02854e-05 | 0.005014 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386484 | CAGTGACGCCCCAGC[A/G]GAGGTCGATTCCGTG | 7011 |
rs745761356 | snp | A/G | 4.94303e-05 | 0.00497119 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373116 | AGCCACAGCAGTGAC[A/G]GCTGCAGAACTCCTT | 7011 |
rs745763528 | snp | A/G | 1.70554e-05 | 0.00292017 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382334 | GGGACAGTGGCAGGC[A/G]GGGTCCGGAGTCTCT | 7011 |
rs745781080 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20387168 | TGAACTCCCGACCTC[A/T]GGTGATCTGCCCGCC | 7011 |
rs745795769 | snp | A/G | 6.68338e-05 | 0.00578035 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375815 | GTGACAGGCAGGGAA[A/G]GAGTGGATCAAAACA | 7011 |
rs745806234 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20395334 | AGTTCTGAGCCACTG[A/C]GATGACTGACAAGCA | 7011 |
rs745820072 | snp | A/C | 1.67725e-05 | 0.00289585 | intron-variant | TEP1 | GRCh38.p7 | 14:20381049 | CCCGCTCTGGAGCTG[A/C]GAAGGTCAGATTGAA | 7011 |
rs745822045 | snp | C/T | 1.65488e-05 | 0.00287647 | intron-variant | TEP1 | GRCh38.p7 | 14:20378705 | ACAAATTCACGAGGG[C/T]GAGTCATGGCTCAGG | 7011 |
rs745825745 | snp | A/G | 0.000148315 | 0.00861021 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373033 | GTGGCCACAGCCTTA[A/G]CTTCCTGCCACAAGA | 7011 |
rs745873429 | snp | A/G | 6.58946e-05 | 0.0057396 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401020 | ACGCTTTGTTCCCCC[A/G]TAGGCTCAGCTCCCG | 7011 |
rs745875808 | snp | A/G | 1.7886e-05 | 0.00299044 | intron-variant | TEP1 | GRCh38.p7 | 14:20404793 | ACACAGGGTGAGAGG[A/G]CTAGAATCTCAGTCA | 7011 |
rs745906970 | in-del | -/AGG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393001 | GGCGGGCAGATCACA[-/AGG]AGGAGATCGAGACCA | 7011 |
rs745913276 | snp | A/G | 3.30164e-05 | 0.00406289 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401571 | GACACTGTATCACCG[A/G]CCTTCTCAAACTGTG | 7011 |
rs745936972 | snp | G/T | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387939 | CCAAGGGGCTTGGAG[G/T]GTCCTCTTCCAGTGG | 7011 |
rs745950821 | in-del | -/C | 1.72282e-05 | 0.00293492 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383264 | AGAGGCCTCCAGAGG[-/C]CCCAAGGCCAGCACG | 7011 |
rs746010165 | snp | C/T | 1.64972e-05 | 0.00287199 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381648 | TCAGGGAGGCACAGC[C/T]GGGCACCAGGGCGCT | 7011 |
rs746025487 | snp | C/T | 4.95733e-05 | 0.00497837 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379080 | GCAGAGATTCCATCA[C/T]AGCCACTCACCACAG | 7011 |
rs746032963 | snp | A/T | 7.07389e-05 | 0.0059468 | intron-variant | TEP1 | GRCh38.p7 | 14:20383648 | CACACCAGGCTTCTG[A/T]ACATGGAGAGGAAGT | 7011 |
rs746034727 | snp | C/T | 0.000181194 | 0.00951651 | intron-variant | TEP1 | GRCh38.p7 | 14:20371486 | TGGCATTTTGGATCT[C/T]ACCAGATTTCAGATG | 7011 |
rs746053406 | snp | A/C/G | 5.24043e-05 | 0.00511858 | intron-variant | TEP1 | GRCh38.p7 | 14:20379900 | ATGGATTTTCAGAGG[A/C/G]TAAATTCTGCCCCTC | 7011 |
rs746097653 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20386335 | TAGTATCCAAGGAGC[A/G]ACTCCCGCCTTCACC | 7011 |
rs746105647 | snp | C/T | 3.64292e-05 | 0.0042677 | intron-variant | TEP1 | GRCh38.p7 | 14:20377795 | ATACCACCTCCACCA[C/T]GCGGTCCTCCTTCCT | 7011 |
rs746151531 | snp | C/G | 1.7479e-05 | 0.00295621 | intron-variant | TEP1 | GRCh38.p7 | 14:20395672 | AGGCAGCTTCTATTC[C/G]CTCATCTTTTCCTAC | 7011 |
rs746194589 | snp | C/T | 3.45985e-05 | 0.00415909 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396658 | ATGAGCTCATGGTGG[C/T]GGGAACTGATTCCAA | 7011 |
rs746209428 | snp | A/C | 8.26644e-05 | 0.00642848 | intron-variant | TEP1 | GRCh38.p7 | 14:20403901 | TGTCAAAGAGAGAGG[A/C]GAGACCACTAGAAGC | 7011 |
rs746214691 | snp | C/G | 1.71067e-05 | 0.00292456 | intron-variant | TEP1 | GRCh38.p7 | 14:20369296 | TATAGGTGTGAGCCA[C/G]TGCTCCCAGCCCTCC | 7011 |
rs746233871 | snp | A/G | 1.92287e-05 | 0.00310064 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383891 | CCTTGGCCCCATCAG[A/G]AGCCTGCAGGGCTGA | 7011 |
rs746249663 | snp | C/T | 1.73249e-05 | 0.00294315 | intron-variant | TEP1 | GRCh38.p7 | 14:20391135 | AATAAAGCTCCCCTG[C/T]TTTGGAATTCACCCT | 7011 |
rs746270229 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20390354 | CTATATCAGGAGTGT[C/G]AGAATACTACACAGC | 7011 |
rs746273158 | snp | C/T | 2.78975e-05 | 0.0037347 | intron-variant | TEP1 | GRCh38.p7 | 14:20396739 | CCATTTTCTGTGGAA[C/T]GTGGGGCATAGAGTG | 7011 |
rs746289308 | snp | A/C | 1.70531e-05 | 0.00291997 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368872 | GCAACTCAGGTAGCA[A/C]ATGGAGGGCTGTGAC | 7011 |
rs746338095 | snp | C/T | 1.64827e-05 | 0.00287073 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382692 | CGGCCGGCCTGATTC[C/T]CGCTTCACCAGCAGC | 7011 |
rs746341746 | snp | A/G | 1.65982e-05 | 0.00288077 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376225 | GCCTTGTGTGGCCGC[A/G]TCAGCAGCTGCCTTG | 7011 |
rs746355359 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378445 | AGCTGCCTGTGGCTA[C/T]TACCTGCCCCTCTGG | 7011 |
rs746361335 | in-del | -/C | 1.67531e-05 | 0.00289418 | intron-variant | TEP1 | GRCh38.p7 | 14:20384728 | GCTGACCACCAAAGA[-/C]CCCAAAAGTTGGAAT | 7011 |
rs746395991 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20378318 | TGCTGCTGTCTGTCG[C/T]CTGCCACCCTCCACT | 7011 |
rs746422411 | snp | A/C | 3.67931e-05 | 0.00428896 | intron-variant | TEP1 | GRCh38.p7 | 14:20376310 | TCCTGAAAGAGGAAG[A/C]CAGACAGGCCCTGGG | 7011 |
rs746457866 | snp | A/G | 3.29522e-05 | 0.00405894 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377608 | TCAGTACCTGAAGAG[A/G]TTTTGTAGATCCTAA | 7011 |
rs746534380 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408002 | GAGCAGGCAATTGCT[A/G]TTGTTCACACGGTAC | 7011 |
rs746558139 | snp | A/G | 3.29984e-05 | 0.00406179 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381969 | GTAGGGGTCTCCACT[A/G]TTACCAGCAGCCACT | 7011 |
rs746574126 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394200 | CAGCACCTCAGCCTC[C/T]CAAGTAGGTGGGACT | 7011 |
rs746588098 | snp | C/T | 3.29712e-05 | 0.00406011 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383489 | CTTCTCACACTCACC[C/T]GGGGAAGCTTCTTTG | 7011 |
rs746604244 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409738 | AATTAAGAAAAATGC[C/T]GGCCGGGCGCGGTGG | 7011 |
rs746608963 | snp | A/G | 1.68261e-05 | 0.00290048 | intron-variant | TEP1 | GRCh38.p7 | 14:20389792 | ATGCTAGACAGCCCA[A/G]GACATTAAGATATGA | 7011 |
rs746628975 | snp | C/T | 3.29457e-05 | 0.00405854 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372754 | TTTCCGGGTGCCGAA[C/T]CCTTCCGCAGTTTCA | 7011 |
rs746641306 | snp | A/T | 1.65113e-05 | 0.00287322 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382033 | GTCCGCCACACACTC[A/T]GCACTCCGTGCAGCT | 7011 |
rs746642603 | in-del | -/G | 1.64806e-05 | 0.00287054 | intron-variant | TEP1 | GRCh38.p7 | 14:20373488 | ACCTCCCTTGACTCT[-/G]GTCCTTGCAGGAACT | 7011 |
rs746648822 | snp | C/G | 1.67795e-05 | 0.00289646 | intron-variant | TEP1 | GRCh38.p7 | 14:20373838 | CACAAGATCAGAGCA[C/G]AGTCATATTGAGCAG | 7011 |
rs746652978 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376755 | TTACTGGGAGGTTAG[A/G]GGTCCCAGAATGAAG | 7011 |
rs746671394 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375073 | TCCAGCCTGGGCAAC[A/G]AGAACGAAACTCTGT | 7011 |
rs746681464 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411261 | AACACCCCGATCTAA[C/G]CCTCAGCACTCTAAG | 7011 |
rs746688175 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368120 | GGTCCTAGGGCCCGC[A/G]AGTGATGCAAGAATT | 7011 |
rs746695887 | in-del | -/C | 1.65138e-05 | 0.00287343 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378178 | GGCCCACAGCCACAA[-/C]CCCCCCCAGGCACAT | 7011 |
rs746701748 | snp | C/G | 1.7521e-05 | 0.00295976 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374440 | TCACCACAGCTGCCA[C/G]AGCGCTCACAGCACT | 7011 |
rs746754959 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372550 | GGCCCAGAGCTTGGC[A/T]TCAAGTAGGCACCTG | 7011 |
rs746761827 | snp | C/T | 1.66952e-05 | 0.00288917 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20376103 | TCCTTCTGCAGCTCA[C/T]CCGATCCCGGCCCCC | 7011 |
rs746773848 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409974 | TTGCAGTGAGCCCAG[A/G]TTGGCCACTGCACTC | 7011 |
rs746809216 | snp | A/G | 1.66192e-05 | 0.00288259 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401128 | GAGAAAAGAGCTGTA[A/G]GTTGGAGGGGTATCT | 7011 |
rs746845018 | snp | C/T | 1.66877e-05 | 0.00288852 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386539 | TCGGGCCTGCAGTGC[C/T]GGCAGCACAGACCTC | 7011 |
rs746880272 | snp | C/G | 1.72946e-05 | 0.00294058 | intron-variant | TEP1 | GRCh38.p7 | 14:20381079 | ATTCATTAGGGATAT[C/G]AAGGGGCTGGTGAGA | 7011 |
rs746888444 | snp | C/T | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415511 | AGGTGGGCAGATTAC[C/T]TGAGGTCAGGAGTTT | 7011 |
rs746891466 | snp | G/T | 3.29794e-05 | 0.00406061 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381362 | GGGCAACTTCGGAAG[G/T]TGCCTGAGGCATCAG | 7011 |
rs746895844 | snp | A/C | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384473 | CCGCCAACATAGGGC[A/C]GGCCAGCTGCCACAC | 7011 |
rs746903948 | snp | A/T | | | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391644 | GTCTGCATTAGCATC[A/T]GTCAGATAGACCAAG | 7011 |
rs746916035 | in-del | -/AGGATGTCTGGATGGGC | 1.65263e-05 | 0.00287452 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408396 | CGGTTCTCCAAGGAG[-/AGGATGTCTGGATGGGC]AGACACATGCCCATG | 7011 |
rs746935421 | snp | A/G | 1.64857e-05 | 0.00287099 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378817 | GCTCAGGCAGCAGCC[A/G]GTGATTTGGTACTGG | 7011 |
rs746949348 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant | TEP1 | GRCh38.p7 | 14:20384552 | AGAGCAGGCCCGGCT[C/T]CTCTCACCACATCTC | 7011 |
rs746967740 | snp | A/G | 1.65097e-05 | 0.00287308 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377489 | CCCTGAGCCCCCTGG[A/G]AACCTAGAGAATGAG | 7011 |
rs746977192 | snp | A/G | 1.65586e-05 | 0.00287733 | intron-variant | TEP1 | GRCh38.p7 | 14:20401434 | ACTTAGATGGAATGC[A/G]TGCTCAGGGTGCAGC | 7011 |
rs747006676 | snp | A/C | 1.72579e-05 | 0.00293746 | intron-variant | TEP1 | GRCh38.p7 | 14:20395419 | GTAGCCCCGATTGCC[A/C]ACCCTTGGCTCCCAG | 7011 |
rs747095936 | snp | C/T | 9.89022e-05 | 0.00703145 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385076 | GCATCACCTCCATCT[C/T]TGTCACAGAGCGCCC | 7011 |
rs747119691 | in-del | -/A | 1.66603e-05 | 0.00288615 | intron-variant | TEP1 | GRCh38.p7 | 14:20391808 | GGGGCTCAGGGACTT[-/A]ATCTGCCCCTTAGAG | 7011 |
rs747136487 | snp | C/G | 3.29609e-05 | 0.00405948 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390946 | GTCTGACCTGGACTT[C/G]AGCCTGGAGCTTGAT | 7011 |
rs747141949 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20383710 | GGTGGTACGTGGGCA[A/T]CAACAAGGCTGGGCT | 7011 |
rs747153558 | snp | G/T | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380019 | AGAAGGCCACAGCAG[G/T]AGGGGATGAGGAAAC | 7011 |
rs747170040 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406836 | ATCTGATAGGGCCAC[C/T]GGGAAATTAAATGGA | 7011 |
rs747170152 | snp | A/C/G | 1.65097e-05 | 0.00287308 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395562 | GAAACCTCCGCCTGG[A/C/G]ACGGTTCTTTTCATT | 7011 |
rs747172102 | snp | C/T | 1.658e-05 | 0.00287919 | intron-variant | TEP1 | GRCh38.p7 | 14:20368603 | CAGGGCTACAAGCCT[C/T]CTTACTAACTTATTT | 7011 |
rs747187563 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408240 | GGGTGGGCAGACACA[C/T]ATCCATGTGGTTTTT | 7011 |
rs747193522 | snp | A/G | 1.66277e-05 | 0.00288333 | intron-variant | TEP1 | GRCh38.p7 | 14:20395981 | GGAGGGGTCATGAGC[A/G]CAGGAGCCGGGAGTA | 7011 |
rs747230496 | snp | C/T | 1.67697e-05 | 0.00289561 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375850 | TTTTGGGTGTCCTCA[C/T]GTCCCAGCAGAGGAG | 7011 |
rs747241041 | in-del | -/GGGG | 1.64754e-05 | 0.00287009 | intron-variant | TEP1 | GRCh38.p7 | 14:20386232 | CGTGTGGGAGTCACT[-/GGGG]GCATGGTATCAGGGA | 7011 |
rs747277088 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366919 | AAGCATGGGCCAAGG[A/G]CAGGAGGAAGCTCTA | 7011 |
rs747328928 | snp | C/T | 0.000115522 | 0.00759919 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384138 | TGAAGAAGGCGTGGC[C/T]GGGCAGGACTCGGTG | 7011 |
rs747331834 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20381221 | GAGGGGTAATGGCGG[C/T]GGTGATGGTGGAGAT | 7011 |
rs747343842 | snp | C/T | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401008 | CCTCCCAGACCGACG[C/T]TTTGTTCCCCCGTAG | 7011 |
rs747367659 | snp | C/T | 4.94205e-05 | 0.0049707 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387956 | TCCTCTTCCAGTGGC[C/T]GGAGAGACTGGACCC | 7011 |
rs747371963 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400741 | GTACTTTTGTCATAT[A/G]TTGATAAAAACTTGT | 7011 |
rs747381986 | snp | C/T | 0.000112009 | 0.00748279 | intron-variant | TEP1 | GRCh38.p7 | 14:20383123 | CACCCCAGGTCCTCA[C/T]AGCTCCCAGATTCAC | 7011 |
rs747385048 | snp | A/T | 4.94271e-05 | 0.00497102 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406255 | TCCTGAAGGACATGG[A/T]CAGTAGGCTCTGGAT | 7011 |
rs747396854 | snp | A/G | 8.23676e-05 | 0.00641693 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391708 | TTCACAGAGAGGTTC[A/G]CAGCTGTCTCTAGGG | 7011 |
rs747419423 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369409 | TGGCATCACTATCCA[C/T]GCTGGCATCAGATTC | 7011 |
rs747495659 | snp | C/T | 4.94752e-05 | 0.00497344 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20388051 | ATGGGAGGCCCCATG[C/T]TCTGCAATGAACCTG | 7011 |
rs747503967 | snp | C/G | 3.31862e-05 | 0.00407333 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377325 | TGGCCAGTCCTAGCA[C/G]AGGCTTCTGGAATCT | 7011 |
rs747509638 | snp | C/T | 0.00105946 | 0.0229915 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383196 | TTAAATGGTGACTCC[C/T]CCAGCCGCTTCCCGT | 7011 |
rs747531900 | snp | A/G | 1.73634e-05 | 0.00294642 | intron-variant | TEP1 | GRCh38.p7 | 14:20379909 | CAGAGGGTAAATTCT[A/G]CCCCTCCTTGATTGT | 7011 |
rs747558783 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20390220 | GGCAACGGAGTGAGA[A/C]CCTGTCTCAAAAAAT | 7011 |
rs747577811 | snp | C/G | 1.6519e-05 | 0.00287388 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406382 | CCCCTTTCTTCTCTT[C/G]TGAATCAAACCAACG | 7011 |
rs747647389 | snp | G/T | 1.6543e-05 | 0.00287597 | intron-variant | TEP1 | GRCh38.p7 | 14:20390641 | AGTTGCAGAGGAAAA[G/T]GTGGGGGAGGGAGAG | 7011 |
rs747659908 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20391191 | CCCTTCCATTGGTTA[C/G]AGGGAATAAGAAAAA | 7011 |
rs747670260 | snp | G/T | 3.29582e-05 | 0.00405931 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380359 | GCTGGTTGGCTGCCT[G/T]CTGGGGCAGGAGCCG | 7011 |
rs747687718 | snp | G/T | 1.65364e-05 | 0.0028754 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368410 | TCTCTAGCACAAGGG[G/T]TATCATTATTCCCGA | 7011 |
rs747697430 | snp | C/T | 1.65842e-05 | 0.00287955 | intron-variant | TEP1 | GRCh38.p7 | 14:20403922 | CACTAGAAGCAAGAC[C/T]CAAACCAACCCTCCA | 7011 |
rs747699766 | snp | A/G | 4.94197e-05 | 0.00497066 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386134 | TGTATCCATAACGGG[A/G]GCCCAGAATCCCCAC | 7011 |
rs747733923 | snp | A/G | 1.654e-05 | 0.00287571 | intron-variant | TEP1 | GRCh38.p7 | 14:20403701 | AAAGGGGCGTGGGTC[A/G]AGGGCTGGGGCAGTG | 7011 |
rs747749338 | in-del | -/TT/TTT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394474 | ACTGGCCCCTTGGGC[-/TT/TTT]TTTTTTTTTTTTTTT | 7011 |
rs747754111 | snp | C/G | 1.64871e-05 | 0.00287111 | intron-variant | TEP1 | GRCh38.p7 | 14:20372964 | CAGTAAATACACAGC[C/G]AGGGTAGAATTCACA | 7011 |
rs747789293 | snp | C/T | 1.67419e-05 | 0.00289321 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384081 | TGCCCCGTCACCAGG[C/T]TCAGCCTTCCGTGGG | 7011 |
rs747789335 | snp | C/G | 1.68855e-05 | 0.00290559 | intron-variant | TEP1 | GRCh38.p7 | 14:20369311 | CTGCTCCCAGCCCTC[C/G]CCTAGTATTTCTGAC | 7011 |
rs747820694 | snp | A/G | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378460 | TTACCTGCCCCTCTG[A/G]GTGGAAGGCAACACA | 7011 |
rs747823982 | in-del | -/GGAGAAGCAGCTT | 1.81513e-05 | 0.00301253 | intron-variant | TEP1 | GRCh38.p7 | 14:20382397 | TTCAGTGCAGTGGGA[-/GGAGAAGCAGCTT]GGCTTGTGGGATAGG | 7011 |
rs747832015 | snp | A/C/G | 0.000201264 | 0.0100299 | intron-variant | TEP1 | GRCh38.p7 | 14:20374559 | GTCAGAAGTCAGAGG[A/C/G]GTGGGATTATCAGCA | 7011 |
rs747858037 | snp | A/G | 4.95921e-05 | 0.00497932 | intron-variant | TEP1 | GRCh38.p7 | 14:20396770 | AGAAAAACAAATGAG[A/G]AGGCCAGGCACAGTG | 7011 |
rs747860112 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408703 | CCAGGTGCAGTGGCT[C/T]ATGCCTGTAATCCCA | 7011 |
rs747932527 | snp | A/C | 3.29788e-05 | 0.00406058 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405535 | GTCAGATGTATTGTT[A/C]ATGTTTACTTCTGAG | 7011 |
rs747940733 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384483 | AGGGCCGGCCAGCTG[C/T]CACACCCCCCCACTC | 7011 |
rs747944020 | snp | A/G | 4.94271e-05 | 0.00497102 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369718 | ATTAGGGTCCTACTA[A/G]GATTCTCTAAGTTTA | 7011 |
rs747956803 | snp | A/C/T | 3.35685e-05 | 0.00409674 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386483 | TCAGTGACGCCCCAG[A/C/T]GGAGGTCGATTCCGT | 7011 |
rs747971587 | snp | A/T | 3.3976e-05 | 0.00412151 | intron-variant | TEP1 | GRCh38.p7 | 14:20369825 | TACCCATATGAGTCA[A/T]CTTGTACCAGACAAA | 7011 |
rs747974670 | snp | G/T | 3.30404e-05 | 0.00406437 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395573 | CTGGGACGGTTCTTT[G/T]CATTTCTAGTTAGTA | 7011 |
rs747982685 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20371463 | TTTTTCCCCAGCTCA[G/T]GAGGAAATGGCATTT | 7011 |
rs748004225 | snp | C/T | 3.30022e-05 | 0.00406202 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395507 | TACAACACAGGTATC[C/T]TCATTGCCATCCGAA | 7011 |
rs748015266 | in-del | -/ACA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20412132 | CCAGGGCCAAAAAGG[-/ACA]ACAATATCTCACTGG | 7011 |
rs748025044 | snp | C/T | 3.29522e-05 | 0.00405894 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373359 | GAAACAGCAGCAGCA[C/T]GGACTGGGCCGCTGT | 7011 |
rs748026841 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20384326 | CCAAGCTACTTCCTC[C/T]CCAGGACAACCCAGA | 7011 |
rs748042124 | snp | A/G | 8.26194e-05 | 0.00642673 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382041 | CACACTCAGCACTCC[A/G]TGCAGCTGGTCCACA | 7011 |
rs748047108 | snp | A/G | 4.94817e-05 | 0.00497377 | intron-variant | TEP1 | GRCh38.p7 | 14:20378971 | AAGACAAATGGGGAG[A/G]ACCCCTTACCGACAA | 7011 |
rs748048653 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383495 | ACACTCACCCGGGGA[A/G]GCTTCTTTGGGATCC | 7011 |
rs748052680 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372451 | GTCTGAATAGTGCTG[C/G]TGGTTTAAATATATG | 7011 |
rs748058065 | snp | C/T | 6.60578e-05 | 0.0057467 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379073 | CAAACAAGCAGAGAT[C/T]CCATCACAGCCACTC | 7011 |
rs748073046 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408010 | AATTGCTGTTGTTCA[C/T]ACGGTACAAATCAGC | 7011 |
rs748096009 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377612 | TACCTGAAGAGATTT[C/T]GTAGATCCTAATGCC | 7011 |
rs748098305 | snp | A/G | 3.49083e-05 | 0.00417767 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383610 | ACTCAGCAGACTTGG[A/G]CAGCAGCCTCTGCTG | 7011 |
rs748135609 | in-del | -/CACACACACT | 3.37018e-05 | 0.00410485 | intron-variant | TEP1 | GRCh38.p7 | 14:20368776 | ACGCACACACACACA[-/CACACACACT]CACACACACACACAC | 7011 |
rs748141570 | in-del | -/ACTA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20370200 | TTACAGGCGTGAGCC[-/ACTA]ACTACACCTGGGTAA | 7011 |
rs748166959 | snp | A/G | 1.6693e-05 | 0.00288898 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368844 | ACATCTCTGTCCTTC[A/G]AAGCTGTCACCAGCA | 7011 |
rs748195963 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408351 | TGTAGTTTCTCCAAG[A/G]GCTGTAAGTCAGGGA | 7011 |
rs748205898 | snp | C/T | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381036 | GAAGTCCACGGTTCC[C/T]GCTCTGGAGCTGAGA | 7011 |
rs748208828 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374627 | GAAGGCGGTTAGCCA[C/T]GTAATTAAGGGCCTG | 7011 |
rs748221863 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383853 | ACGAGCCCCAGAAAA[A/G]TGGAAGAAGACTAAT | 7011 |
rs748247327 | snp | C/G | 1.64906e-05 | 0.00287142 | intron-variant | TEP1 | GRCh38.p7 | 14:20404805 | AGGACTAGAATCTCA[C/G]TCACTCCTCCCGTAG | 7011 |
rs748253952 | snp | A/G/T | 7.87221e-05 | 0.00627342 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383794 | TGGCCACGCAGATAG[A/G/T]TACAGAGGCGTCTGA | 7011 |
rs748274661 | snp | A/G | 1.73854e-05 | 0.00294829 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382355 | CGGAGTCTCTCAGAC[A/G]CCTAGGATGGCGGGA | 7011 |
rs748279170 | snp | C/T | 1.64838e-05 | 0.00287083 | intron-variant | TEP1 | GRCh38.p7 | 14:20373262 | GTCTCTCTCCAAGCC[C/T]CACTCACCTGCTTCC | 7011 |
rs748326672 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405047 | ACCTCCTGCATCAAC[A/G]GCTATCAAAAATTTA | 7011 |
rs748367494 | snp | C/T | 1.66515e-05 | 0.00288539 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376111 | CAGCTCACCCGATCC[C/T]GGCCCCCGGTGGCCA | 7011 |
rs748381845 | in-del | -/TGAGCACAGGAGCCGGGAG | 1.65919e-05 | 0.00288022 | intron-variant | TEP1 | GRCh38.p7 | 14:20395976 | AGGAGGGAGGGGTCA[-/TGAGCACAGGAGCCGGGAG]TATGGGGGGCTTCAG | 7011 |
rs748402200 | snp | A/G | 4.94703e-05 | 0.0049732 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377461 | GGCGGACACTGCCAC[A/G]TCCAGTGCCTGACCC | 7011 |
rs748410198 | snp | C/G/T | 3.31149e-05 | 0.00406898 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406396 | TCTGAATCAAACCAA[C/G/T]GACCCTGGGGTAGTA | 7011 |
rs748414519 | snp | A/T | 1.651e-05 | 0.0028731 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405551 | ATGTTTACTTCTGAG[A/T]CCAGAGTAGAGCACA | 7011 |
rs748431021 | in-del | -/A | 0.000133231 | 0.00816075 | intron-variant | TEP1 | GRCh38.p7 | 14:20406417 | TGGGGTAGTAGTGGC[-/A]GTTATGAATCACAGC | 7011 |
rs748452682 | snp | A/C/G | 3.29572e-05 | 0.00405928 | intron-variant | TEP1 | GRCh38.p7 | 14:20373627 | GAAGGGACGGAGCAG[A/C/G]GGAGAAAAGAAGAGA | 7011 |
rs748469667 | in-del | -/CT | 1.65259e-05 | 0.00287449 | intron-variant | TEP1 | GRCh38.p7 | 14:20378271 | TGGAAACGTGAAGAC[-/CT]GCTCTCAGCAAAATC | 7011 |
rs748475879 | snp | C/T | 3.29919e-05 | 0.00406138 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380946 | CATAGAGGGCATGGG[C/T]CTCCAAGAGCCGAGA | 7011 |
rs748477871 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367066 | AATTTTAGAAATATA[A/C]TAAAGTTCTTTTATG | 7011 |
rs748496660 | snp | C/G | 1.65723e-05 | 0.00287852 | intron-variant | TEP1 | GRCh38.p7 | 14:20388077 | ACCTGACATAAATAA[C/G]AAGATAAATGAGAGT | 7011 |
rs748502043 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409592 | CCCAAATCCATTCCC[A/C]TTCCTTTGCCCCCTT | 7011 |
rs748513347 | in-del | -/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20386700 | ACTGCTGTGATCACC[-/C]TTTAGCACTGAGCAC | 7011 |
rs748513886 | snp | A/G | 3.31774e-05 | 0.00407279 | intron-variant | TEP1 | GRCh38.p7 | 14:20403682 | GTCCTGCCCTTCCTG[A/G]AGAAAAGGGGCGTGG | 7011 |
rs748522564 | snp | C/G | 1.66418e-05 | 0.00288455 | intron-variant | TEP1 | GRCh38.p7 | 14:20381907 | GCTCTGCTGGGGCAC[C/G]TGTACCTGCGCAGAC | 7011 |
rs748551588 | snp | A/G | 1.65239e-05 | 0.00287431 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389282 | TGTCACATCATTGGG[A/G]TTCAAATCTGTTGAC | 7011 |
rs748560358 | snp | A/G | 1.8014e-05 | 0.00300111 | intron-variant | TEP1 | GRCh38.p7 | 14:20407845 | AACAGACATGGCTGG[A/G]GTCAAGATGAGTGCC | 7011 |
rs748573909 | snp | A/T | 1.65452e-05 | 0.00287616 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380031 | CAGTAGGGGATGAGG[A/T]AACTGCCAGAGACAG | 7011 |
rs748607656 | snp | C/G | 1.67452e-05 | 0.0028935 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371625 | GTAGAATTCGGTTCA[C/G]GTGAAGACTAGCTCA | 7011 |
rs748625955 | snp | C/T | 1.65021e-05 | 0.00287241 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385101 | GCGCCCTGAAGGGTA[C/T]TGCTGGGCCTGCGGG | 7011 |
rs748637666 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367913 | CATGCCCGGCCTCCT[A/C]TGGGTAGTTCTGAGA | 7011 |
rs748639775 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397402 | TAATCCCAGCCACTC[A/G]AAAGGCTGAGTCAGG | 7011 |
rs748648622 | snp | G/T | 4.94719e-05 | 0.00497328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373706 | CATGGCAGCTGCACA[G/T]TGGCTAATGGGTCCT | 7011 |
rs748652594 | snp | A/G | 1.64991e-05 | 0.00287215 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381951 | GGCAAACGGGCCCAT[A/G]GGGTAGGGGTCTCCA | 7011 |
rs748658939 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400675 | TGTGCCAGTCCTACC[A/T]TTTTTGGAATGAGTT | 7011 |
rs748658942 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371529 | GCTTCATGCAAAGTA[A/G]CTTCAAATCTGCTTT | 7011 |
rs748688616 | snp | C/T | 8.25389e-05 | 0.0064236 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378075 | CGCATGCAGGAAAAG[C/T]GCAGCAGCAACAAAG | 7011 |
rs748707767 | snp | C/T | 3.39225e-05 | 0.00411826 | intron-variant | TEP1 | GRCh38.p7 | 14:20380211 | CTCTGGTGGGCTTAC[C/T]AGGGTCTGGGGTCAA | 7011 |
rs748722679 | snp | A/G | 1.65641e-05 | 0.00287781 | intron-variant | TEP1 | GRCh38.p7 | 14:20400939 | AAATGTGGAGGCATA[A/G]ATGGGGAAGAGAAGG | 7011 |
rs748733284 | snp | G/T | 1.7426e-05 | 0.00295173 | intron-variant | TEP1 | GRCh38.p7 | 14:20386407 | CACCACTCAAGCCCC[G/T]CATCCCCGACCCAGC | 7011 |
rs748785055 | snp | C/T | 1.65302e-05 | 0.00287486 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404692 | CAGGTGGGGGCGACA[C/T]GCCGGCAAGAAAGCA | 7011 |
rs748800734 | snp | A/T | 1.64803e-05 | 0.00287052 | intron-variant | TEP1 | GRCh38.p7 | 14:20373005 | ACCAAGGGTACACCG[A/T]CTCACCTGTGCTGTG | 7011 |
rs748802057 | in-del | -/ACACACA | 5.04804e-05 | 0.00502371 | intron-variant | TEP1 | GRCh38.p7 | 14:20368780 | CACACACACACACAC[-/ACACACA]CACACACTTACCAGC | 7011 |
rs748818857 | snp | A/G | 1.65004e-05 | 0.00287227 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378470 | CTCTGGGTGGAAGGC[A/G]ACACAGTTCAGGGAC | 7011 |
rs748832660 | snp | A/G | 1.65056e-05 | 0.00287272 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384154 | GGGCAGGACTCGGTG[A/G]CTTCTGCAGCTGCTG | 7011 |
rs748869140 | snp | A/C | 1.68363e-05 | 0.00290136 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386477 | TCCTCCTCAGTGACG[A/C]CCCAGCGGAGGTCGA | 7011 |
rs748870461 | snp | C/G | 1.6507e-05 | 0.00287284 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380935 | ACTCATCTCACCATA[C/G]AGGGCATGGGCCTCC | 7011 |
rs748873272 | snp | C/G | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413991 | CAAGTGCCTCCCCTC[C/G]TGTTGATCAGAAGAG | 7011 |
rs748887873 | snp | G/T | 1.67368e-05 | 0.00289277 | intron-variant | TEP1 | GRCh38.p7 | 14:20384265 | AGTGACTATCCATGG[G/T]GCCATGCTCCTCAGC | 7011 |
rs748918528 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394638 | GCACCCACCACCACA[C/T]CCGGCTAATTTTTGT | 7011 |
rs748921052 | snp | A/G/T | 0.000148506 | 0.00861596 | synonymous-codon, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378792 | CGGTGGCTAGCAGCC[A/G/T]GCAGTCTGGGCTCAG | 7011 |
rs748939265 | snp | C/T | 5.08591e-05 | 0.00504252 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383208 | TCCTCCAGCCGCTTC[C/T]CGTACAGGGCCAGCT | 7011 |
rs748944853 | snp | C/G/T | 6.62005e-05 | 0.00575297 | intron-variant | TEP1 | GRCh38.p7 | 14:20378703 | GAACAAATTCACGAG[C/G/T]GTGAGTCATGGCTCA | 7011 |
rs748950266 | snp | C/G | 6.63515e-05 | 0.00575946 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391094 | TGCATAGTTCAGCGG[C/G]GGCTGATTGGACAAG | 7011 |
rs748959109 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402672 | TCATAGCCAGTAAGG[A/G]GTGGATGGAAGATTC | 7011 |
rs749009664 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391721 | TCACAGCTGTCTCTA[A/G]GGCCTGTCGGTACCT | 7011 |
rs749016451 | snp | C/G | 1.64942e-05 | 0.00287173 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377696 | AGAGGGCAGGAGAGA[C/G]AGAAAGGGAACCCAG | 7011 |
rs749029585 | snp | G/T | 1.64871e-05 | 0.00287111 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383515 | CTTTGGGATCCAGTC[G/T]GAAATCAGCTGCCCA | 7011 |
rs749073105 | snp | A/C | 1.64743e-05 | 0.00287 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403377 | GAAGAAGGGACTCAC[A/C]TTTCTCTGCTCTTCT | 7011 |
rs749093576 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408113 | GGTGGCCAGGCACCG[G/T]TTCTCCAAGGAGAGG | 7011 |
rs749127281 | snp | C/T | 1.72027e-05 | 0.00293275 | intron-variant | TEP1 | GRCh38.p7 | 14:20395656 | GGTAAATTTCCGAGT[C/T]AGGCAGCTTCTATTC | 7011 |
rs749143028 | snp | A/G | 2.03685e-05 | 0.00319121 | intron-variant | TEP1 | GRCh38.p7 | 14:20383696 | AAAAAAAAAGCAGGG[A/G]TGGTACGTGGGCATC | 7011 |
rs749150318 | snp | A/T | 0.000214124 | 0.0103449 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371276 | ATGCCATACTCCTTG[A/T]GGGTGGACAATATCA | 7011 |
rs749154105 | snp | A/C | 1.75289e-05 | 0.00296043 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383635 | CTGCTGCAGCTCCCA[A/C]ACCAGGCTTCTGTAC | 7011 |
rs749176737 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20396207 | GGTGTGGTAGCTCAC[A/G]CCTGTAATCCCAGCA | 7011 |
rs749193909 | snp | A/C | 1.65583e-05 | 0.00287731 | intron-variant | TEP1 | GRCh38.p7 | 14:20382176 | GGGAACCAATGTAAT[A/C]CGAACCCTGGCCCTC | 7011 |
rs749211990 | in-del | -/G | 0.00057644 | 0.0169673 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369375 | GTCTTTAGATGTGGT[-/G]TTGGCTCACTATCCA | 7011 |
rs749221387 | snp | A/C/T | 0.000122013 | 0.00780984 | intron-variant | TEP1 | GRCh38.p7 | 14:20374569 | AGAGGAGTGGGATTA[A/C/T]CAGCATCCCTCCAGC | 7011 |
rs749248366 | snp | A/G | 1.76058e-05 | 0.00296692 | intron-variant | TEP1 | GRCh38.p7 | 14:20404565 | GCAGTGAGCATAAGA[A/G]AAGGAATGAAGTGAA | 7011 |
rs749255224 | snp | C/T | 1.67351e-05 | 0.00289263 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380459 | GAGCTTTTGTTCCTC[C/T]TTGGGGACTGAAGAA | 7011 |
rs749264986 | snp | G/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408218 | GTTCTCCAAGGAGAG[G/T]ATGTCTGGGTGGGCA | 7011 |
rs749341656 | snp | A/C | 3.30196e-05 | 0.00406309 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405552 | TGTTTACTTCTGAGA[A/C]CAGAGTAGAGCACAG | 7011 |
rs749390159 | snp | A/G | 6.59152e-05 | 0.00574049 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382682 | GCAGGTAGAGCGGCC[A/G]GCCTGATTCCCGCTT | 7011 |
rs749401376 | snp | A/G | 0.0002096 | 0.010235 | intron-variant | TEP1 | GRCh38.p7 | 14:20386651 | AGAGAGCTGGGCTCA[A/G]TCTAGGGATGATTCC | 7011 |
rs749408845 | snp | A/G | 1.64781e-05 | 0.00287033 | intron-variant | TEP1 | GRCh38.p7 | 14:20384584 | GTACAGGTGCTCCCT[A/G]CCTCCCTCAGCTCAC | 7011 |
rs749430556 | snp | A/C | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386492 | CCCCAGCGGAGGTCG[A/C]TTCCGTGAAGGCTGA | 7011 |
rs749437260 | snp | A/G | 4.9467e-05 | 0.00497303 | intron-variant | TEP1 | GRCh38.p7 | 14:20381542 | CCCAGGCTGACTTGG[A/G]CTGCAATCACCTGCA | 7011 |
rs749476588 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20373463 | GAAGGTTATTCCGCA[C/T]ACCTTCCCCACCTCC | 7011 |
rs749490336 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20404149 | CACCTGAGGTCAGGC[A/G]TTCAAGACCAGCCTG | 7011 |
rs749513366 | snp | G/T | 1.73531e-05 | 0.00294555 | intron-variant | TEP1 | GRCh38.p7 | 14:20376286 | TGGAAAAAGAGAGAG[G/T]GAACAGCTTCCTGAA | 7011 |
rs749529494 | snp | A/G | 4.94279e-05 | 0.00497107 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373367 | AGCAGCACGGACTGG[A/G]CCGCTGTGTCCCAGG | 7011 |
rs749530355 | snp | C/T | 0.000198321 | 0.00995596 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379077 | CAAGCAGAGATTCCA[C/T]CACAGCCACTCACCA | 7011 |
rs749570245 | snp | C/G | 3.29549e-05 | 0.00405911 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403745 | CGGGGTGGCCGGCGG[C/G]GGTGTCTCTTGGCCC | 7011 |
rs749602668 | snp | C/T | 1.65051e-05 | 0.00287267 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389623 | ACAGGTATTGTACCC[C/T]TCTTAGGAGGATACC | 7011 |
rs749678385 | snp | A/G | 1.68564e-05 | 0.00290309 | intron-variant | TEP1 | GRCh38.p7 | 14:20380222 | TTACTAGGGTCTGGG[A/G]TCAAGGTCTTACCTT | 7011 |
rs749712575 | snp | C/T | 3.35278e-05 | 0.00409424 | intron-variant | TEP1 | GRCh38.p7 | 14:20386049 | TTGCTTCCTCCCCAG[C/T]CCTCCTCCAAACCTG | 7011 |
rs749735851 | snp | A/G | 8.24844e-05 | 0.00642148 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378177 | CCGGCCCACAGCCAC[A/G]ACCCCCCCAGGCACA | 7011 |
rs749740650 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408509 | CCTGGCTGCACTGAG[C/T]GTGTATTTGCATGAG | 7011 |
rs749744739 | snp | C/T | 1.67719e-05 | 0.0028958 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368858 | CGAAGCTGTCACCAG[C/T]AACTCAGGTAGCACA | 7011 |
rs749767632 | snp | C/T | 1.91963e-05 | 0.00309802 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383868 | GTGGAAGAAGACTAA[C/T]GATGCCACCTTGGCC | 7011 |
rs749781918 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20379842 | AATTAATCAGAGTGA[C/T]AACAGGTGTGTTTGG | 7011 |
rs749796153 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372749 | TCAAATTTCCGGGTG[C/T]CGAACCCTTCCGCAG | 7011 |
rs749797673 | in-del | -/GA | 1.66824e-05 | 0.00288806 | intron-variant | TEP1 | GRCh38.p7 | 14:20378542 | GTCCCACAGCTGAGG[-/GA]GAGAGAGGAGGAATC | 7011 |
rs749820806 | snp | C/G | 1.74634e-05 | 0.0029549 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384048 | TGTACCAGGAAGGCT[C/G]TCTTGCCCTGTCCTG | 7011 |
rs749829724 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409181 | CTTTATCTTATTTCA[C/T]CCCTCAAGTAGAATA | 7011 |
rs749829957 | snp | A/G/T | 0.000214784 | 0.0103612 | intron-variant | TEP1 | GRCh38.p7 | 14:20378263 | GGTAGAAATGGAAAC[A/G/T]TGAAGACCTGCTCTC | 7011 |
rs749836374 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397926 | CCTGGCTAATTTTTG[C/T]ATTTTTAGTAGAGAC | 7011 |
rs749845921 | in-del | -/T | 1.64819e-05 | 0.00287066 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382688 | GAGCGGCCGGCCTGA[-/T]TTCCCGCTTCACCAG | 7011 |
rs749856919 | snp | C/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391050 | TCCACCTGCTCCGCC[C/G]TCGTGATCATCATCC | 7011 |
rs749864592 | snp | A/C | 1.74233e-05 | 0.0029515 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396631 | CATACCGCATGCTGG[A/C]GTCTCTGGAGAATGA | 7011 |
rs749880807 | snp | C/G | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381349 | CAGAGCCTCAGGAGG[C/G]CAACTTCGGAAGGTG | 7011 |
rs749883511 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20396146 | TAACAAAAGAAGAGA[A/C]AGTAACAGAAGGAGC | 7011 |
rs749915862 | snp | G/T | 1.66754e-05 | 0.00288746 | intron-variant | TEP1 | GRCh38.p7 | 14:20405417 | CCCAGTCTACCAGCT[G/T]CACACCCCCATCCCC | 7011 |
rs749923223 | in-del | -/CG | 0.000193272 | 0.00982846 | intron-variant | TEP1 | GRCh38.p7 | 14:20368763 | AGGTGTGCAGGCGCA[-/CG]CACACACACACACAC | 7011 |
rs749951619 | snp | A/G | 3.2994e-05 | 0.00406152 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391078 | TCCCAATCAACAGCA[A/G]TGCATAGTTCAGCGG | 7011 |
rs749963171 | snp | A/C/G | 3.29529e-05 | 0.00405901 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405489 | GGAGGGCAAGTTCAC[A/C/G]ACAGATTTCAAAAAT | 7011 |
rs749967736 | snp | C/G/T | 3.2948e-05 | 0.00405871 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382657 | AGCCTCAGGTGATCG[C/G/T]TGACCAAGCGCAGGT | 7011 |
rs749969019 | snp | G/T | 1.65836e-05 | 0.0028795 | intron-variant | TEP1 | GRCh38.p7 | 14:20401428 | GGAATTACTTAGATG[G/T]AATGCATGCTCAGGG | 7011 |
rs749984247 | snp | A/G | 3.3157e-05 | 0.00407154 | intron-variant | TEP1 | GRCh38.p7 | 14:20369785 | CCTTTTGCCTCTGTG[A/G]AAGAATAGGTAATTT | 7011 |
rs750010712 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397371 | AAAATTAGCCAGGCG[G/T]GGTGTCTGGTGCCTC | 7011 |
rs750018411 | snp | A/G | 1.64762e-05 | 0.00287016 | stop-gained, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401509 | TGTGGATGTGCAGTC[A/G]CTGAACCAGCTTCTT | 7011 |
rs750118597 | snp | A/G | 1.6904e-05 | 0.00290719 | intron-variant | TEP1 | GRCh38.p7 | 14:20380088 | AAAGGGAGGAAATAA[A/G]CGAGAGAATGCAAAC | 7011 |
rs750133308 | snp | C/T | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385045 | GGCTGCAGACGTTGG[C/T]TCCGGTTCAGGAACT | 7011 |
rs750133510 | snp | C/T | 4.94678e-05 | 0.00497307 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379040 | GGCAGTAAGAAAGAG[C/T]GTATCATCGGAGAGG | 7011 |
rs750133965 | snp | C/G | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413813 | AGATTTTAGCATGCT[C/G]GCTGCCTAGCTGTAC | 7011 |
rs750153172 | snp | A/G | 1.65203e-05 | 0.002874 | intron-variant | TEP1 | GRCh38.p7 | 14:20403710 | TGGGTCGAGGGCTGG[A/G]GCAGTGACTGACTGG | 7011 |
rs750214181 | in-del | -/AAG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20387561 | CGTCTCAAAAAAAAA[-/AAG]AAATTAAGCAACTAA | 7011 |
rs750222612 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400180 | ATTATCTACATATAC[C/T]GGCTTCTATCCAGGC | 7011 |
rs750229679 | snp | A/G | 0.000132214 | 0.00812954 | intron-variant | TEP1 | GRCh38.p7 | 14:20368586 | ACAAAAATAGGGGAG[A/G]TCAGGGCTACAAGCC | 7011 |
rs750229758 | snp | C/G | 1.7789e-05 | 0.00298231 | intron-variant | TEP1 | GRCh38.p7 | 14:20371680 | TCCTATTTTAGTTAA[C/G]CTTTCTCAGGCTCCT | 7011 |
rs750262745 | snp | A/G | 1.6563e-05 | 0.00287771 | intron-variant | TEP1 | GRCh38.p7 | 14:20395966 | TAGAAAGCAAAGGAG[A/G]GAGGGGTCATGAGCA | 7011 |
rs750276408 | snp | G/T | 1.97058e-05 | 0.00313887 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383777 | CACCTGGCTCTTTTA[G/T]TTGGCCACGCAGATA | 7011 |
rs750307915 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20379263 | TCAAGTGGGGGCCTC[A/G]TGATCCAAGTGGGGC | 7011 |
rs750313942 | in-del | -/CTTA | 1.64849e-05 | 0.00287092 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377431 | ACCAATACCTTGGGG[-/CTTA]CTTAGCCAGGCCAGG | 7011 |
rs750317620 | snp | C/T | 0.00205615 | 0.0319976 | intron-variant | TEP1 | GRCh38.p7 | 14:20368795 | ACACACACACACACT[C/T]ACCAGCTGCATACTG | 7011 |
rs750317763 | snp | C/G | 1.8261e-05 | 0.00302162 | intron-variant | TEP1 | GRCh38.p7 | 14:20396609 | CCATGGCTACCAGCC[C/G]CTCACACATACCGCA | 7011 |
rs750318587 | snp | G/T | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378127 | GCCAGCCGTGCCCCT[G/T]CTCGCCAGGCCCACA | 7011 |
rs750318768 | snp | A/G | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405473 | ATAAACTCAGGCTCC[A/G]GGAGGGCAAGTTCAC | 7011 |
rs750329849 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391031 | ACCTCCACACAGCAC[A/G]ACGTCCACCTGCTCC | 7011 |
rs750347118 | in-del | -/TG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376605 | TTCCACCTCGTGACC[-/TG]TGAGGACCAGTTCTC | 7011 |
rs750381601 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406302 | AGAGGTGAGCTTCAC[A/G]GCCAGATCCTCCACC | 7011 |
rs750390336 | in-del | -/A | 1.79719e-05 | 0.0029976 | intron-variant | TEP1 | GRCh38.p7 | 14:20380520 | AGCCAGCTGGACCCC[-/A]ATTAGCCCCAGCACC | 7011 |
rs750397747 | snp | A/G | 1.64795e-05 | 0.00287045 | intron-variant | TEP1 | GRCh38.p7 | 14:20382573 | AGACAAAGCAGCTGA[A/G]GAGAGAATGGGAAGT | 7011 |
rs750403125 | snp | A/C | 1.68468e-05 | 0.00290226 | intron-variant | TEP1 | GRCh38.p7 | 14:20376078 | GAGGCTATGGGACCC[A/C]AGGGTTGCATCCTTC | 7011 |
rs750415032 | snp | C/T | 1.66084e-05 | 0.00288165 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377320 | GGAAGTGGCCAGTCC[C/T]AGCACAGGCTTCTGG | 7011 |
rs750418565 | snp | C/T | 1.65075e-05 | 0.00287289 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378221 | TACGGATAGAGGCTC[C/T]GGGTGCCCCCAGGTC | 7011 |
rs750425227 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20379792 | GATTTTTTGGCCAAG[C/G]CCTTTGAGCTGATGT | 7011 |
rs750448242 | snp | A/C | 1.65332e-05 | 0.00287512 | intron-variant | TEP1 | GRCh38.p7 | 14:20378746 | CCACTGCAGACCCCA[A/C]GTCTTACCTTTAGGC | 7011 |
rs750463784 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391689 | CAGCAGGGGCAGGCT[A/G]TGCTTCACAGAGAGG | 7011 |
rs750474330 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393388 | CCCAGCACTATCCAA[C/T]AGAATTCAATTACAA | 7011 |
rs750480623 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411471 | AGCCTGTGCTGACAC[A/C]AAGCCCCAGTCTGAT | 7011 |
rs750494035 | in-del | -/A | 3.29481e-05 | 0.00405869 | intron-variant | TEP1 | GRCh38.p7 | 14:20371327 | CTCCTGGTTTGTGAG[-/A]AAGGAATAGGTTGAG | 7011 |
rs750495252 | snp | A/C/T | 3.3004e-05 | 0.00406216 | intron-variant | TEP1 | GRCh38.p7 | 14:20369643 | CCCTGGGCCATCTCC[A/C/T]GGCTCCTCAGGTCCT | 7011 |
rs750587612 | snp | C/G | 1.75863e-05 | 0.00296527 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383188 | CCTGGTTGTTAAATG[C/G]TGACTCCTCCAGCCG | 7011 |
rs750611706 | snp | A/C/G | 0.000115677 | 0.00760438 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389247 | ACTCACTTCAGTATC[A/C/G]CATCAGTACAGCCTG | 7011 |
rs750618841 | snp | C/T | 1.67318e-05 | 0.00289234 | intron-variant | TEP1 | GRCh38.p7 | 14:20389570 | AGGAAATGTAGACCA[C/T]TGATTTCTGACACTG | 7011 |
rs750628647 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20413336 | GCGCCCTAGACCCAG[A/G]GCCAGGGCAAGTTCT | 7011 |
rs750641641 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409073 | CTATTCACTCTTTAA[C/T]CAACTAAATGGGATT | 7011 |
rs750642658 | snp | C/G | 1.71814e-05 | 0.00293094 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383260 | GAGCAGAGGCCTCCA[C/G]AGGCCCCAAGGCCAG | 7011 |
rs750642834 | snp | A/G | 3.46111e-05 | 0.00415985 | intron-variant | TEP1 | GRCh38.p7 | 14:20381716 | GGAAGGGAGAGAGAA[A/G]AAGGAAGAGGCCTGT | 7011 |
rs750654054 | snp | A/G | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377423 | GCACCACTCACCAAT[A/G]CCTTGGGGCTTAGCC | 7011 |
rs750666810 | snp | C/G | 1.80448e-05 | 0.00300368 | intron-variant | TEP1 | GRCh38.p7 | 14:20407825 | AGCTAGAGACAAGAG[C/G]ATACAACAGACATGG | 7011 |
rs750697781 | snp | A/G | 0.000214796 | 0.0103611 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381930 | GCGCAGACTCTGGAC[A/G]AGGCAGGCAAACGGG | 7011 |
rs750706683 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367830 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 7011 |
rs750713280 | snp | A/G | 1.64923e-05 | 0.00287156 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403480 | AGCAATTTCAAAAAA[A/G]GGGAACTGGCTGTCC | 7011 |
rs750776365 | snp | A/G | | | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408182 | CATGGTCTTCAGGTC[A/G]GAAAGTGTGGCCAGG | 7011 |
rs750786204 | snp | A/C | 1.64789e-05 | 0.0028704 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390717 | AGACAGCAGGTATTT[A/C]CCAAAAGTATTCAGG | 7011 |
rs750806580 | in-del | -/C | 1.828e-05 | 0.00302319 | intron-variant | TEP1 | GRCh38.p7 | 14:20404811 | AGAATCTCAGTCACT[-/C]CTCCCGTAGCTTTCT | 7011 |
rs750822620 | snp | A/C | 3.42255e-05 | 0.00413661 | intron-variant | TEP1 | GRCh38.p7 | 14:20375737 | TGGGCTCTGTGCCAC[A/C]CCTGGCCCTTTACTC | 7011 |
rs750845140 | snp | C/T | 6.61201e-05 | 0.00574941 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404677 | ACAGAAATATCGTCG[C/T]AGGTGGGGGCGACAC | 7011 |
rs750852071 | snp | A/G | 3.29516e-05 | 0.00405891 | intron-variant | TEP1 | GRCh38.p7 | 14:20386235 | GTGGGAGTCACTGGG[A/G]GCATGGTATCAGGGA | 7011 |
rs750864595 | snp | C/T | 3.30333e-05 | 0.00406393 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382229 | AAGCACTGACCACTC[C/T]GTGTGACTTCTAGGG | 7011 |
rs750908984 | snp | C/T | 3.33067e-05 | 0.00408072 | intron-variant | TEP1 | GRCh38.p7 | 14:20380889 | AAGCACACCCAGGAG[C/T]CCCATATCTCAGAGA | 7011 |
rs750909850 | snp | C/T | 1.66463e-05 | 0.00288494 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384226 | GCTGCTCCAGCAGGG[C/T]CCCAGGCTGAGGGTA | 7011 |
rs750960104 | snp | A/G | 1.66918e-05 | 0.00288888 | intron-variant | TEP1 | GRCh38.p7 | 14:20378544 | CCCACAGCTGAGGGA[A/G]AGAGAGGAGGAATCA | 7011 |
rs750962224 | snp | C/T | 0.000164826 | 0.00907667 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380996 | TGTGCAGCCACCACA[C/T]GGAGGTTGGTAAGGA | 7011 |
rs750963338 | snp | C/T | 8.26959e-05 | 0.0064297 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403497 | GGAACTGGCTGTCCT[C/T]GAAGAGATCCAGTCA | 7011 |
rs750965967 | in-del | -/AG | 0.000131781 | 0.00811621 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391698 | CAGGCTGTGCTTCAC[-/AG]AGAGGTTCACAGCTG | 7011 |
rs750995222 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20369820 | TAGCCTACCCATATG[A/G]GTCAACTTGTACCAG | 7011 |
rs751002055 | snp | A/C | 1.66815e-05 | 0.00288799 | intron-variant | TEP1 | GRCh38.p7 | 14:20406184 | GTACTCCACCACCAA[A/C]CTCCCCTCCACACCA | 7011 |
rs751019207 | snp | A/G | 6.60066e-05 | 0.00574447 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379049 | AAAGAGTGTATCATC[A/G]GAGAGGAACAAACAA | 7011 |
rs751045054 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401526 | TGAACCAGCTTCTTC[A/G]GGGTGAACCTTGGAG | 7011 |
rs751058406 | snp | C/T | 9.88321e-05 | 0.00702896 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371241 | AAAGAACTCCAGGAT[C/T]CTTGGGCTGCAGGAC | 7011 |
rs751106963 | snp | C/T | 1.65021e-05 | 0.00287241 | intron-variant | TEP1 | GRCh38.p7 | 14:20387888 | CAATTCACAAAGGCA[C/T]AGAAACACAGACTGA | 7011 |
rs751109899 | snp | A/G | 0.000115355 | 0.00759368 | intron-variant | TEP1 | GRCh38.p7 | 14:20373434 | GAGATGGGCTCATGA[A/G]AGTGGGCACAACAGA | 7011 |
rs751131104 | snp | A/G | 1.69286e-05 | 0.0029093 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383586 | CCTGGGTCTGGCCAG[A/G]ATGCAGGGACTCAGC | 7011 |
rs751142700 | snp | C/T | 1.68097e-05 | 0.00289906 | splice-acceptor-variant | TEP1 | GRCh38.p7 | 14:20395629 | AGGAAAGGGCAATGC[C/T]GTATGATGACAGGTA | 7011 |
rs751146440 | snp | C/T | 1.64768e-05 | 0.00287021 | intron-variant | TEP1 | GRCh38.p7 | 14:20371343 | AAGGAATAGGTTGAG[C/T]TCAGGATTTAAAGAG | 7011 |
rs751149978 | in-del | -/TCTGAGGCCCTCA | 1.66649e-05 | 0.00288655 | intron-variant | TEP1 | GRCh38.p7 | 14:20382080 | TGAAAACTCAAGCTC[-/TCTGAGGCCCTCA]TCTAACCATACGGTG | 7011 |
rs751160572 | snp | C/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384636 | TGTCTGCTTAGGTAG[C/G]TCTTCAGTTCTGAGA | 7011 |
rs751162044 | snp | C/G | 1.67122e-05 | 0.00289064 | intron-variant | TEP1 | GRCh38.p7 | 14:20379124 | CGACAGTGGGTGAGG[C/G]AGCGCAGCTCAGGCC | 7011 |
rs751213478 | snp | C/T | 1.67649e-05 | 0.0028952 | intron-variant | TEP1 | GRCh38.p7 | 14:20384729 | CTGACCACCAAAGAC[C/T]CCAAAAGTTGGAATA | 7011 |
rs751222200 | snp | C/T | 6.59478e-05 | 0.00574191 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395930 | CTGAATGGAAACTGC[C/T]GACTGTGGATCACCG | 7011 |
rs751237198 | snp | G/T | 3.39951e-05 | 0.00412267 | intron-variant | TEP1 | GRCh38.p7 | 14:20383678 | TCAGGGTCAGTGGGA[G/T]AGAAAAAAAAAGCAG | 7011 |
rs751252366 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401772 | ATGGTAAGCAGCACA[A/G]GATGGCAACTCTTTG | 7011 |
rs751256043 | snp | G/T | 4.95372e-05 | 0.00497656 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378234 | TCCGGGTGCCCCCAG[G/T]TCCTACACAGGGAGG | 7011 |
rs751268859 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400417 | ATTACAAAGACCTTG[C/T]CTCTAAAATTTAAAA | 7011 |
rs751290580 | snp | A/G | 2.13728e-05 | 0.00326893 | intron-variant | TEP1 | GRCh38.p7 | 14:20368910 | GAGTGAATCTCAAAG[A/G]GGAAAGGGGAGAGCA | 7011 |
rs751297426 | snp | C/T | 1.67125e-05 | 0.00289067 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377745 | CAGAGACCCTGACCA[C/T]ACCTGAACCTGGGAA | 7011 |
rs751304753 | snp | A/C/T | 1.77836e-05 | 0.00298186 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396621 | GCCCCTCACACATAC[A/C/T]GCATGCTGGAGTCTC | 7011 |
rs751319771 | snp | G/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408080 | GCTGGCAGACACAGT[G/T]CTCTTTAGACTAGAG | 7011 |
rs751348235 | snp | A/T | 1.79123e-05 | 0.00299263 | intron-variant | TEP1 | GRCh38.p7 | 14:20408476 | TGCCTAGAAGGAGAG[A/T]AAGACAGGAGATGAG | 7011 |
rs751390803 | snp | A/G | | | | | GRCh38.p7 | 14:20416521 | AGGACCCAGGCATCA[A/G]TAGTTTTTGAAGTTT | 7011 |
rs751402575 | snp | C/T | 1.66654e-05 | 0.00288659 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368827 | GTCTCTCCCATAGCT[C/T]AACATCTCTGTCCTT | 7011 |
rs751412269 | snp | A/T | 1.64784e-05 | 0.00287035 | intron-variant | TEP1 | GRCh38.p7 | 14:20382581 | CAGCTGAAGAGAGAA[A/T]GGGAAGTAGTGATTA | 7011 |
rs751412481 | snp | C/G | 2.03519e-05 | 0.00318991 | intron-variant | TEP1 | GRCh38.p7 | 14:20383961 | GTCACATTTTACATG[C/G]CTGAGCTCCCTGTGC | 7011 |
rs751420264 | in-del | -/TTGTGGTTTTTT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410797 | CTAATTGTTTCTCCT[-/TTGTGGTTTTTT]TTTTTTTTTTTTTTT | 7011 |
rs751448029 | snp | G/T | 1.65302e-05 | 0.00287486 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376175 | TCACAGGGCCCTCAT[G/T]TCCCCGCAGCTCAGT | 7011 |
rs751449109 | snp | A/G | 3.29538e-05 | 0.00405904 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373328 | AGAGGCGGTCAGCAT[A/G]AGGCCTGAGGTTTCT | 7011 |
rs751451548 | snp | C/G | 1.70775e-05 | 0.00292207 | intron-variant | TEP1 | GRCh38.p7 | 14:20391576 | CAACCCAACCCCTTG[C/G]AGGATGCTTTTTGTT | 7011 |
rs751465522 | snp | C/T | 4.94238e-05 | 0.00497086 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382666 | TGATCGGTGACCAAG[C/T]GCAGGTAGAGCGGCC | 7011 |
rs751487541 | in-del | -/CAA | 2.04466e-05 | 0.00319732 | intron-variant | TEP1 | GRCh38.p7 | 14:20383711 | GTGGTACGTGGGCAT[-/CAA]CAAGGCTGGGCTCAT | 7011 |
rs751495777 | snp | A/G | 0.000103538 | 0.00719432 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386619 | AAAGCCGGATGCTGC[A/G]CCATCTGGGGATAAG | 7011 |
rs751536418 | snp | A/G | 6.59489e-05 | 0.00574196 | intron-variant | TEP1 | GRCh38.p7 | 14:20378368 | CCCAAGAGCAACACT[A/G]GACCTTCTTACCTTG | 7011 |
rs751539517 | snp | C/T | 1.65053e-05 | 0.0028727 | intron-variant | TEP1 | GRCh38.p7 | 14:20381427 | AGATATTGAGAAAGG[C/T]TCAGCCCTGCATCAT | 7011 |
rs751544169 | snp | C/T | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373699 | GGGGCTCCATGGCAG[C/T]TGCACAGTGGCTAAT | 7011 |
rs751564082 | snp | C/T | 1.69203e-05 | 0.00290859 | splice-acceptor-variant | TEP1 | GRCh38.p7 | 14:20376265 | GCACTGTGAAATCCT[C/T]TGCATTGGAAAAAGA | 7011 |
rs751569123 | snp | C/G | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405513 | CAAAAATGGCAGCCA[C/G]GGTGGGGTCAGATGT | 7011 |
rs751575092 | snp | C/T | 1.65236e-05 | 0.00287429 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389278 | AGAGTGTCACATCAT[C/T]GGGATTCAAATCTGT | 7011 |
rs751588457 | snp | C/T | 8.24599e-05 | 0.00642053 | intron-variant | TEP1 | GRCh38.p7 | 14:20377554 | AGGGGGCAGGGGCTG[C/T]GCTCTTTCTAAAGGC | 7011 |
rs751602231 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375512 | TGACCTTGGAAATGT[G/T]CTGAGTTCAATTTCC | 7011 |
rs751615315 | snp | C/G | 1.8038e-05 | 0.00300311 | intron-variant | TEP1 | GRCh38.p7 | 14:20407832 | GACAAGAGCATACAA[C/G]AGACATGGCTGGAGT | 7011 |
rs751641834 | snp | C/T | 3.31939e-05 | 0.0040738 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373801 | GGCTCACAGACACCA[C/T]GTGCTCCTCCTGCCC | 7011 |
rs751670132 | snp | A/G | 1.64925e-05 | 0.00287158 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407954 | GTCTAGTCCCTTAGA[A/G]AAATGCTGAGCCCTC | 7011 |
rs751678582 | snp | C/T | | | | | GRCh38.p7 | 14:20415677 | GAGGTTGCAGGGAGC[C/T]GAGACCACACCACTG | 7011 |
rs751697201 | snp | A/G | 3.32928e-05 | 0.00407987 | intron-variant | TEP1 | GRCh38.p7 | 14:20389590 | TTCTGACACTGGGCA[A/G]GAAGTATAAGCACCC | 7011 |
rs751721420 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403772 | GCCCGGTGCTTCCGA[A/G]GGTTGTACTTAGCCA | 7011 |
rs751723561 | in-del | -/G | 1.64769e-05 | 0.00287022 | intron-variant | TEP1 | GRCh38.p7 | 14:20372863 | GGCCTGGAGCCTGGT[-/G]TACACAACAAGTTCA | 7011 |
rs751723997 | snp | A/G | 3.4929e-05 | 0.00417891 | intron-variant | TEP1 | GRCh38.p7 | 14:20383396 | AGGTAGAAAGAAAAG[A/G]AGAACCACATTGGAG | 7011 |
rs751730686 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386097 | AAGTGTGGATGGTCA[A/G]GAAGGTTGTAGCTGG | 7011 |
rs751746655 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant | TEP1 | GRCh38.p7 | 14:20372718 | CTATCCCATTAACCC[A/G]TCAGCCTGTTTCACC | 7011 |
rs751753967 | snp | A/G | 8.24831e-05 | 0.00642143 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378119 | GGAAGGCAGCCAGCC[A/G]TGCCCCTTCTCGCCA | 7011 |
rs751757915 | snp | A/C | 1.65059e-05 | 0.00287275 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381940 | TGGACGAGGCAGGCA[A/C]ACGGGCCCATGGGGT | 7011 |
rs751779112 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20391948 | GAGCTTCCCTCTGCC[C/T]CCATCCTATAGGATT | 7011 |
rs751812867 | snp | C/T | 1.64982e-05 | 0.00287208 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382011 | GCTCTTAGTCCCCTT[C/T]GGTAGTGTCCGCCAC | 7011 |
rs751813022 | snp | A/G | 1.70275e-05 | 0.00291778 | intron-variant | TEP1 | GRCh38.p7 | 14:20380101 | AAACGAGAGAATGCA[A/G]ACAGGAGTTGATTTA | 7011 |
rs751840091 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20379461 | GCCTCCCATAAGCAC[A/G]CTGTGCTGCCATAAT | 7011 |
rs751848150 | in-del | -/A | 0.000500757 | 0.0158154 | intron-variant | TEP1 | GRCh38.p7 | 14:20374553 | ACAGAGTCAGAAGTC[-/A]AGAGGAGTGGGATTA | 7011 |
rs751865299 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380290 | GTAGTGTGTGTTGGA[A/G]GTGCCATCTCCGGGA | 7011 |
rs751909774 | snp | A/G | 1.70067e-05 | 0.002916 | intron-variant | TEP1 | GRCh38.p7 | 14:20375912 | TCAGGACCAAAGGAA[A/G]GATGGGAACCCCGGA | 7011 |
rs751915458 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391017 | GTCTTCAGAGTGTCA[C/T]CTCCACACAGCACGA | 7011 |
rs751968808 | snp | C/G | 1.67128e-05 | 0.00289069 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386511 | CGTGAAGGCTGATAC[C/G]GTGAGGGGCCGCTCG | 7011 |
rs751992143 | snp | C/T | 3.29881e-05 | 0.00406115 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401106 | CAAGGCCCAGGAAGG[C/T]GACTTCGAGAAAAGA | 7011 |
rs752000704 | in-del | -/CCTCC | 3.34185e-05 | 0.00408756 | intron-variant | TEP1 | GRCh38.p7 | 14:20406183 | GTACTCCACCACCAA[-/CCTCC]CCTCCCCTCCACACC | 7011 |
rs752004025 | snp | C/G | 1.66674e-05 | 0.00288676 | intron-variant | TEP1 | GRCh38.p7 | 14:20384238 | GGGCCCCAGGCTGAG[C/G]GTAAATGGGTCAGTG | 7011 |
rs752007131 | in-del | -/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409431 | TGCTGGCGACTCACA[-/G]GATCTATTCCTGGAC | 7011 |
rs752011484 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20412194 | ATGGCTTCTGTGCCC[A/G]ATACACTTTGCTCAT | 7011 |
rs752012955 | snp | C/G | 3.29728e-05 | 0.00406021 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373096 | ATGGAACCATCTGGT[C/G]CCCAAGCCACAGCAG | 7011 |
rs752041439 | snp | C/T | 1.66603e-05 | 0.00288615 | intron-variant | TEP1 | GRCh38.p7 | 14:20391808 | AGGGGCTCAGGGACT[C/T]ATCTGCCCCTTAGAG | 7011 |
rs752043739 | snp | A/G | 3.2963e-05 | 0.00405961 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378851 | GCCTTAGTCTGCAGC[A/G]CCCTATCCCAGGAAG | 7011 |
rs752049484 | snp | C/T | 3.29848e-05 | 0.00406095 | intron-variant | TEP1 | GRCh38.p7 | 14:20369647 | GGGCCATCTCCCGGC[C/T]CCTCAGGTCCTCCTG | 7011 |
rs752057643 | snp | A/C | 0.00021931 | 0.0104693 | intron-variant | TEP1 | GRCh38.p7 | 14:20401175 | GAGGTCTATCATTTC[A/C]GAGTCAGCAAGAAAA | 7011 |
rs752083004 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20370352 | TTTCCCATCAATACC[A/G]GACCATCACCACAAA | 7011 |
rs752099970 | snp | A/C | 3.29772e-05 | 0.00406048 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377448 | TTAGCCAGGCCAGGG[A/C]GGACACTGCCACATC | 7011 |
rs752121384 | snp | C/G | 6.58935e-05 | 0.00573955 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403427 | TTGGAAAACATCTGT[C/G]AGAAAATGGAGGCTC | 7011 |
rs752140895 | snp | A/G | 1.66134e-05 | 0.00288208 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379949 | CAAGTTCTCAGGTCC[A/G]ACAGGTAAACTGTCC | 7011 |
rs752150379 | snp | A/C | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408209 | CAGGCACTGGTTCTC[A/C]AAGGAGAGGATGTCT | 7011 |
rs752172777 | snp | G/T | 1.66668e-05 | 0.00288672 | intron-variant | TEP1 | GRCh38.p7 | 14:20395837 | GGGAGGCAAAGAGGA[G/T]TTGGAAGAAAGGGGA | 7011 |
rs752181848 | snp | A/G | 1.64885e-05 | 0.00287123 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368473 | CACATTGCCCTGCAC[A/G]TCTCCCACGGCAAGC | 7011 |
rs752191544 | snp | A/G | 1.70061e-05 | 0.00291595 | intron-variant | TEP1 | GRCh38.p7 | 14:20377765 | GAACCTGGGAACCAA[A/G]AAAAGGGCTTAAGGA | 7011 |
rs752215847 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374042 | CTTTACACCAACCCT[C/T]AGCCTCAACACCATA | 7011 |
rs752219081 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388127 | TCAGTGAGGTCTTCC[A/G]AAAAGGGCAGGGGGA | 7011 |
rs752243107 | snp | C/G | | | | | GRCh38.p7 | 14:20416299 | CCATAAATATCAGAC[C/G]TGAGAAGACTGGCAA | 7011 |
rs752272754 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375343 | GTATCTTTAGTAGAG[A/G]CAGGGTTTCTCCATG | 7011 |
rs752275576 | in-del | -/TTT | 0.000231321 | 0.0107521 | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389249 | CACTTCAGTATCGCA[-/TTT]TCAGTACAGCCTGAG | 7011 |
rs752285923 | snp | A/C | 1.65468e-05 | 0.00287631 | intron-variant | TEP1 | GRCh38.p7 | 14:20390804 | TGCACAGTAAGCGAC[A/C]AACACTGCAGTCTTG | 7011 |
rs752287032 | snp | C/G | 3.33795e-05 | 0.00408517 | intron-variant | TEP1 | GRCh38.p7 | 14:20378010 | AACCCACCACCAGCC[C/G]TCTGCAAGCTGACCT | 7011 |
rs752287494 | snp | A/T | 1.64803e-05 | 0.00287052 | intron-variant | TEP1 | GRCh38.p7 | 14:20371365 | TTTAAAGAGAGGTAA[A/T]GAGAAGAACACCTCT | 7011 |
rs752309024 | snp | A/C | 2.00495e-05 | 0.00316613 | intron-variant | TEP1 | GRCh38.p7 | 14:20383683 | GTCAGTGGGAGAGAA[A/C]AAAAAAGCAGGGGTG | 7011 |
rs752319692 | snp | C/T | 1.65743e-05 | 0.00287869 | intron-variant | TEP1 | GRCh38.p7 | 14:20380911 | TCTCAGAGAAGAACC[C/T]AGCCAGTGACTCATC | 7011 |
rs752333908 | in-del | -/A | 1.95326e-05 | 0.00312505 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383910 | CTGCAGGGCTGACAC[-/A]AGAGATGCCTGCATG | 7011 |
rs752340084 | snp | A/G | 1.6819e-05 | 0.00289987 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375760 | CTTTACTCACCAGTA[A/G]GTTATCTTTGGTCCA | 7011 |
rs752349458 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405267 | AACAAACCAAGTCTA[A/G]TATACTCTTTCCCCA | 7011 |
rs752417148 | snp | C/T | 6.63735e-05 | 0.00576041 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382297 | CTTCTCCAGTGTGCT[C/T]AGGATGTGCTGCAGC | 7011 |
rs752451189 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408281 | CAGGTCAGGAAGCGT[A/G]GCTAGGCACTGGTTC | 7011 |
rs752463115 | snp | A/G | 3.2956e-05 | 0.00405918 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369358 | CCTTTCTACGCTGCC[A/G]TGTCTTTAGATGTGG | 7011 |
rs752472847 | snp | C/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387910 | ACAGACTGACCCTTG[C/G]TGGGAAACAGGAGCC | 7011 |
rs752490785 | snp | A/G | 1.70301e-05 | 0.00291801 | intron-variant | TEP1 | GRCh38.p7 | 14:20376272 | GAAATCCTCTGCATT[A/G]GAAAAAGAGAGAGGG | 7011 |
rs752505594 | snp | C/T | 1.6528e-05 | 0.00287467 | intron-variant | TEP1 | GRCh38.p7 | 14:20382720 | AGCAGTCGCATCTGG[C/T]AAGACTCAGGACTCA | 7011 |
rs752510796 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367760 | ACTACAGGTGCCCGC[C/T]GCCACACCTGGCTAA | 7011 |
rs752522280 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371261 | GGCTGCAGGACAAAT[A/G]TGCCATACTCCTTGT | 7011 |
rs752539395 | snp | A/G | 3.29489e-05 | 0.00405874 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391665 | ATAGACCAAGACAGT[A/G]CGGCCTGGCAGCAGG | 7011 |
rs752541836 | snp | A/G | 1.73132e-05 | 0.00294216 | intron-variant | TEP1 | GRCh38.p7 | 14:20377275 | TGCCCACTGTCTAGT[A/G]GTACCTGAGGCAGAA | 7011 |
rs752604869 | snp | C/T | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381606 | CTCTTCCCATAGCAA[C/T]GTTTAGCTGCTGTTC | 7011 |
rs752629183 | snp | A/G | 4.94303e-05 | 0.00497119 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387992 | TTTCCTGGGGGTGGT[A/G]GAATCTTGAATATTT | 7011 |
rs752632251 | snp | C/G/T | 1.64754e-05 | 0.00287009 | missense, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384644 | TAGGTAGCTCTTCAG[C/G/T]TCTGAGATCCGACGT | 7011 |
rs752635625 | snp | A/G | | | | | GRCh38.p7 | 14:20416018 | AGGAGTTTGGTGAGG[A/G]AACACAAGAGCTAGG | 7011 |
rs752650770 | snp | C/T | 0.000115313 | 0.0075923 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380301 | TGGAGGTGCCATCTC[C/T]GGGAGAGCAGCGAGG | 7011 |
rs752659901 | snp | A/C | 1.68502e-05 | 0.00290255 | intron-variant | TEP1 | GRCh38.p7 | 14:20379143 | GCAGCTCAGGCCATC[A/C]CCTTGACCCTCCAAG | 7011 |
rs752659958 | snp | C/T | 5.07352e-05 | 0.00503637 | intron-variant | TEP1 | GRCh38.p7 | 14:20381696 | AGCAAACTGTCCTCG[C/T]GTGAGGAAGGGAGAG | 7011 |
rs752684008 | snp | C/T | 1.68863e-05 | 0.00290566 | intron-variant | TEP1 | GRCh38.p7 | 14:20384743 | CCCCAAAAGTTGGAA[C/T]AGACTCAGACCCCAG | 7011 |
rs752753539 | snp | C/T | 1.67262e-05 | 0.00289185 | intron-variant | TEP1 | GRCh38.p7 | 14:20382088 | CAAGCTCTCTGAGGC[C/T]CTCATCTAACCATAC | 7011 |
rs752764529 | snp | A/G | 3.29451e-05 | 0.00405851 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372801 | TTTCTCATCAGCACT[A/G]AGGACAAAAAAGGTG | 7011 |
rs752819904 | snp | C/T | 3.32027e-05 | 0.00407434 | splice-acceptor-variant | TEP1 | GRCh38.p7 | 14:20389742 | ATGACCCTGTCCACC[C/T]GTAAGATGAAAAGGG | 7011 |
rs752823565 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20401438 | AGATGGAATGCATGC[A/T]CAGGGTGCAGCTTCT | 7011 |
rs752854519 | snp | A/G | 4.94344e-05 | 0.00497139 | intron-variant | TEP1 | GRCh38.p7 | 14:20372872 | CCTGGTGTACACAAC[A/G]AGTTCAATTCAGTGC | 7011 |
rs752862513 | snp | A/C/G | 4.29759e-05 | 0.00463535 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396711 | CCGAAGCATGGCCAT[A/C/G]AAGGGAAGCTTCCCA | 7011 |
rs752871371 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386113 | GAAGGTTGTAGCTGG[A/G]GGGAATGTATCCATA | 7011 |
rs752879365 | in-del | -/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388824 | ATGCCTGGATGGCTG[-/T]AAAAGAGGAGTGAAC | 7011 |
rs752900860 | snp | A/G | 6.72653e-05 | 0.00579898 | intron-variant | TEP1 | GRCh38.p7 | 14:20368917 | TCTCAAAGAGGAAAG[A/G]GGAGAGCAGAATGGT | 7011 |
rs752911295 | snp | C/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402190 | GTGGATGTCTGTACT[C/T]CCAGCTACTCGGGAG | 7011 |
rs752921392 | snp | C/T | 1.80039e-05 | 0.00300027 | intron-variant | TEP1 | GRCh38.p7 | 14:20384010 | ACAGCCTTCCCTCCC[C/T]CCTGCCCAGGCCCCT | 7011 |
rs752928641 | snp | C/T | 4.94214e-05 | 0.00497074 | intron-variant | TEP1 | GRCh38.p7 | 14:20386205 | AGTTGTCTGTAGGCA[C/T]GATGATAGGGACGTG | 7011 |
rs752931941 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20390848 | AAATCTTCAGAACTG[C/T]GTATTGTCTGTGCCT | 7011 |
rs752947660 | snp | C/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380402 | GAGGATTGAAGCCTG[C/G]TGCCTCAGGAAGGTG | 7011 |
rs752952976 | snp | A/G | 1.65173e-05 | 0.00287374 | intron-variant | TEP1 | GRCh38.p7 | 14:20378251 | CCTACACAGGGAGGT[A/G]GAAATGGAAACGTGA | 7011 |
rs752974270 | snp | C/T | 8.23852e-05 | 0.00641762 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382677 | CAAGCGCAGGTAGAG[C/T]GGCCGGCCTGATTCC | 7011 |
rs753026915 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401499 | TGGGCAGGCTTGTGG[A/G]TGTGCAGTCGCTGAA | 7011 |
rs753047835 | snp | A/G | 1.64817e-05 | 0.00287064 | intron-variant | TEP1 | GRCh38.p7 | 14:20378869 | CTATCCCAGGAAGAT[A/G]AAGTCAGTCCTCTGG | 7011 |
rs753064543 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409741 | TAAGAAAAATGCTGG[C/T]CGGGCGCGGTGGCTC | 7011 |
rs753076343 | snp | A/T | 1.89795e-05 | 0.00308048 | intron-variant | TEP1 | GRCh38.p7 | 14:20401188 | TCAGAGTCAGCAAGA[A/T]AATAACTCAGAAAAG | 7011 |
rs753079996 | snp | C/T | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395543 | TGACGGCTTAGGTGG[C/T]AAAGAAACCTCCGCC | 7011 |
rs753114132 | snp | A/C | 1.7658e-05 | 0.00297131 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383286 | GCCAGCACGTGGGCA[A/C]CCTGGCTCTGCTCAA | 7011 |
rs753121851 | snp | C/G | 1.6476e-05 | 0.00287014 | intron-variant | TEP1 | GRCh38.p7 | 14:20384538 | AGCACAACCAGGTCA[C/G]AGCAGGCCCGGCTCC | 7011 |
rs753129797 | snp | C/T | 1.65921e-05 | 0.00288024 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395473 | GTGTACTCTCAGCTT[C/T]TCCCTCTTGAGCTGC | 7011 |
rs753141989 | snp | C/T | 4.94328e-05 | 0.00497131 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373308 | AGCCGTACAGAACCA[C/T]CCTCAGAGGCGGTCA | 7011 |
rs753146872 | snp | C/T | 1.64798e-05 | 0.00287047 | intron-variant | TEP1 | GRCh38.p7 | 14:20369669 | GTCCTCCTGTTACCA[C/T]TCACCAGATTCAGGT | 7011 |
rs753190676 | snp | A/C | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377643 | ATCCGCTCGATATCC[A/C]ACAGCCACCCGATCA | 7011 |
rs753211124 | snp | C/T | 0.000131837 | 0.00811795 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407967 | GAGAAATGCTGAGCC[C/T]TCCAACTTGGAGGCT | 7011 |
rs753261828 | snp | A/G | 0.000509285 | 0.0159494 | intron-variant | TEP1 | GRCh38.p7 | 14:20368770 | CAGGCGCACGCACAC[A/G]CACACACACACACAC | 7011 |
rs753288715 | snp | C/T | 1.68995e-05 | 0.00290679 | intron-variant | TEP1 | GRCh38.p7 | 14:20376067 | TAGGAACTAGAGAGG[C/T]TATGGGACCCCAGGG | 7011 |
rs753293804 | snp | A/C | 4.94923e-05 | 0.0049743 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378117 | AGGGAAGGCAGCCAG[A/C]CGTGCCCCTTCTCGC | 7011 |
rs753298033 | snp | A/C/G | 3.29453e-05 | 0.00405854 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408289 | GAAGCGTGGCTAGGC[A/C/G]CTGGTTCTTCAAGGA | 7011 |
rs753314249 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368948 | GAGTTCTCAGGGGCC[C/T]CTCCTCAGAGAAGCA | 7011 |
rs753322277 | in-del | -/A | 1.6612e-05 | 0.00288196 | intron-variant | TEP1 | GRCh38.p7 | 14:20368606 | GCTACAAGCCTCCTT[-/A]ACTAACTTATTTTTT | 7011 |
rs753351570 | snp | C/G | 1.71143e-05 | 0.00292521 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404751 | TCCGGACGTTCAGCT[C/G]CTGCCTGGCATACAA | 7011 |
rs753353523 | snp | A/G | 1.68812e-05 | 0.00290522 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408428 | AGACACATGCCCATG[A/G]AGTTTTTCCATGGCT | 7011 |
rs753360171 | snp | A/G | 1.96103e-05 | 0.00313126 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383809 | GTACAGAGGCGTCTG[A/G]GCAGAGTGAGGGCAA | 7011 |
rs753374801 | snp | C/T | 1.65051e-05 | 0.00287267 | intron-variant | TEP1 | GRCh38.p7 | 14:20390904 | GGCCTGTGTCCTTCA[C/T]GTATTTTTGGATGGT | 7011 |
rs753378510 | snp | A/G | 4.94548e-05 | 0.00497242 | intron-variant | TEP1 | GRCh38.p7 | 14:20373171 | GAAAGGACGTGTTTC[A/G]TTAGGAGCTGGGATA | 7011 |
rs753415986 | snp | C/T | 3.30082e-05 | 0.00406239 | intron-variant | TEP1 | GRCh38.p7 | 14:20368563 | GAACAGGCCCAGCTA[C/T]GATGGGAACAAAAAT | 7011 |
rs753431034 | in-del | -/G | 3.31389e-05 | 0.00407042 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391092 | AGTGCATAGTTCAGC[-/G]GGGGCTGATTGGACA | 7011 |
rs753439788 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20403665 | CATCAGCATGCTCCC[C/T]TGTCCTGCCCTTCCT | 7011 |
rs753459978 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372016 | CTCCTTACCTTTAGT[A/G]TCTCTCTACTACCAT | 7011 |
rs753467724 | snp | A/G | 1.6808e-05 | 0.00289892 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382320 | GCTGCAGCAGCAGGG[A/G]GACAGTGGCAGGCAG | 7011 |
rs753490697 | snp | A/G | 1.64746e-05 | 0.00287002 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384429 | TATTCCATACATCCT[A/G]CAGAACCAACTGCCC | 7011 |
rs753509255 | snp | A/G | 1.70438e-05 | 0.00291918 | intron-variant | TEP1 | GRCh38.p7 | 14:20381705 | TCCTCGTGTGAGGAA[A/G]GGAGAGAGAAGAAGG | 7011 |
rs753520661 | snp | A/G | 1.82261e-05 | 0.00301872 | intron-variant | TEP1 | GRCh38.p7 | 14:20382402 | TGCAGTGGGAGGAGA[A/G]GCAGCTTGGCTTGTG | 7011 |
rs753529913 | snp | A/G | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377396 | GCCCAGCCCTGCAAG[A/G]ACCCATCTTCTGCAC | 7011 |
rs753534447 | snp | C/T | | | | | GRCh38.p7 | 14:20416206 | CCAACCTCAAGACCT[C/T]GTAGTCTGTGACTCT | 7011 |
rs753534576 | snp | A/G | 3.52653e-05 | 0.00419898 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386586 | CCCCATGCATGTCTC[A/G]GAAAGTGGATGAAAT | 7011 |
rs753546818 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20385226 | CTCCTTCCCTCCAGG[A/C]ACAAGCAATAAAATA | 7011 |
rs753554805 | in-del | -/G | 1.64754e-05 | 0.00287009 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403365 | TATACAACCCCAGAA[-/G]AAGGGACTCACCTTT | 7011 |
rs753556982 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406322 | GATCCTCCACCTCCT[C/T]CTCCTCTCCCAAGCT | 7011 |
rs753574046 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381329 | AGGTGGTAAGGCAGG[C/T]CTCCCAGAGCCTCAG | 7011 |
rs753595800 | in-del | -/GGTT | 1.68316e-05 | 0.00290095 | intron-variant | TEP1 | GRCh38.p7 | 14:20376081 | GCTATGGGACCCCAG[-/GGTT]GCATCCTTCTGCAGC | 7011 |
rs753615869 | snp | A/T | 1.65228e-05 | 0.00287422 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391765 | CCATCATATTTCCAC[A/T]GTCTACATGCAAGAA | 7011 |
rs753626577 | snp | C/T | 1.70837e-05 | 0.00292259 | intron-variant | TEP1 | GRCh38.p7 | 14:20384754 | GGAATAGACTCAGAC[C/T]CCAGCCAGCCTCCCT | 7011 |
rs753627741 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20388011 | TCTTGAATATTTTGT[C/T]CATTTGGCCCACATG | 7011 |
rs753682234 | snp | C/T | 1.65386e-05 | 0.00287559 | intron-variant | TEP1 | GRCh38.p7 | 14:20389212 | CAACAAAGTATCCAA[C/T]CCTTCAGTATCCATT | 7011 |
rs753692359 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373102 | CCATCTGGTGCCCAA[-/G]CCACAGCAGTGACGG | 7011 |
rs753717936 | snp | A/C | 1.64781e-05 | 0.00287033 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403462 | CCCTGTAGGGACAGG[A/C]GAAGCAATTTCAAAA | 7011 |
rs753736105 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406653 | CTGCTTTCATCTCTT[C/T]ATTGGCGTCACAACC | 7011 |
rs753761955 | snp | C/T | 1.65312e-05 | 0.00287495 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379964 | AACAGGTAAACTGTC[C/T]CATTGGCAGTGCCCA | 7011 |
rs753768866 | snp | C/T | 1.64988e-05 | 0.00287213 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371593 | ATCCAGACTTGTCAG[C/T]ACCCCTAAGTCCTCC | 7011 |
rs753769564 | snp | A/G | 1.65042e-05 | 0.0028726 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385015 | TCCCGGAAGTAGATG[A/G]GAGCTTGGGCAGAGG | 7011 |
rs753773035 | snp | C/T | 3.30896e-05 | 0.00406739 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395860 | AAAGGGGAGAATACC[C/T]TGATTTCTGAGTTGA | 7011 |
rs753773920 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374730 | CCTTGGGTTTCCCAA[C/T]TATTTAATGAGTATA | 7011 |
rs753794341 | in-del | -/AT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398589 | TATTACACGTAACAC[-/AT]AACACTGTATCATAT | 7011 |
rs753799725 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378404 | TTTGAGCCCATCCAC[C/T]TGGAAGAAGCTGATG | 7011 |
rs753810659 | snp | C/T | 6.63878e-05 | 0.00576103 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378042 | GCCATCCTCTCCAGC[C/T]GTCAGTAACTGGCAA | 7011 |
rs753811113 | snp | A/G | 1.67489e-05 | 0.00289381 | intron-variant | TEP1 | GRCh38.p7 | 14:20380064 | TGGAGCTAGAGAAAG[A/G]GTAGGAAGAAAGGGA | 7011 |
rs753832465 | snp | C/T | 2.49094e-05 | 0.00352903 | missense, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396728 | AGGGAAGCTTCCCAT[C/T]TTCTGTGGAATGTGG | 7011 |
rs753856149 | in-del | -/AG | 1.64859e-05 | 0.002871 | intron-variant | TEP1 | GRCh38.p7 | 14:20372981 | GGGTAGAATTCACAC[-/AG]ACAAAGAACCAAGGG | 7011 |
rs753896916 | snp | A/C | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369366 | CGCTGCCGTGTCTTT[A/C]GATGTGGTGTTGGCT | 7011 |
rs753901702 | snp | G/T | 1.64781e-05 | 0.00287033 | intron-variant | TEP1 | GRCh38.p7 | 14:20372880 | ACACAACAAGTTCAA[G/T]TCAGTGCTTCTGATG | 7011 |
rs753925837 | snp | A/G | 4.96364e-05 | 0.00498154 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404659 | AGGCAGCTGGACAAT[A/G]GCACAGAAATATCGT | 7011 |
rs753937622 | snp | C/T | 3.31455e-05 | 0.00407083 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391605 | TTTTCTTACCCCTTG[C/T]GGGTTGCTCTTTGGA | 7011 |
rs753968764 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410914 | GCAACCTCGACTTCC[C/T]GGGTTCAAGTAATTC | 7011 |
rs753973228 | snp | C/T | 1.65067e-05 | 0.00287282 | intron-variant | TEP1 | GRCh38.p7 | 14:20400970 | AGGGAATGTGATGGT[C/T]AAGGTCACTCTACCA | 7011 |
rs753991800 | snp | C/T | 0.000115303 | 0.00759199 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369508 | TACCTGTGGTCCATT[C/T]TCCTTCTGGGCTGCA | 7011 |
rs753993589 | snp | A/G | 3.29478e-05 | 0.00405867 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391667 | AGACCAAGACAGTGC[A/G]GCCTGGCAGCAGGGG | 7011 |
rs754031661 | snp | C/T | 1.79939e-05 | 0.00299943 | intron-variant | TEP1 | GRCh38.p7 | 14:20383168 | GGCCCCGGCCTAGAA[C/T]CCAACCTGGTTGTTA | 7011 |
rs754034065 | snp | C/T | 1.65105e-05 | 0.00287315 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384122 | CCGTTGCACTGTGTC[C/T]TGAAGAAGGCGTGGC | 7011 |
rs754063643 | snp | A/T | 1.66018e-05 | 0.00288108 | intron-variant | TEP1 | GRCh38.p7 | 14:20382733 | GGCAAGACTCAGGAC[A/T]CAGGGTGGGGTCCAG | 7011 |
rs754075352 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20401335 | AAGGCAGTCATGTCT[A/G]CAGGGCATGTCTGTC | 7011 |
rs754078113 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368782 | CACACACACACACAC[-/A]CACACACACACTTAC | 7011 |
rs754080151 | snp | C/T | 6.64883e-05 | 0.00576539 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378528 | TGCCCACGGACTGTG[C/T]CCCACAGCTGAGGGA | 7011 |
rs754102597 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388341 | ACGGGGTAGGGAAAG[A/G]TGTAAAGATTAAAGC | 7011 |
rs754110690 | snp | C/T | 9.89201e-05 | 0.00703209 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381634 | TTCTCAGGGGCCCAT[C/T]AGGGAGGCACAGCCG | 7011 |
rs754156808 | snp | C/T | 1.67461e-05 | 0.00289357 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377299 | GGCAGAAGCCAAGAG[C/T]TCCTGGGAAGTGGCC | 7011 |
rs754157637 | snp | A/C | 4.95405e-05 | 0.00497673 | intron-variant | TEP1 | GRCh38.p7 | 14:20406220 | AACCTTCCCCTAACT[A/C]TTGAATTTTTACCTT | 7011 |
rs754201522 | snp | A/G | 1.67321e-05 | 0.00289236 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395621 | ATATTCGAAGGAAAG[A/G]GCAATGCTGTATGAT | 7011 |
rs754205701 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392895 | TTTAAAAATATCTTC[A/C]AAAGAAAAGAAAAAG | 7011 |
rs754209842 | snp | A/G | 8.23689e-05 | 0.00641698 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407985 | CAACTTGGAGGCTCA[A/G]AGAGCAGGCAATTGC | 7011 |
rs754230793 | in-del | -/A | 0.000131799 | 0.00811678 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384495 | CTGCCACACCCCCCC[-/A]CTCACAGGGGTATCT | 7011 |
rs754260162 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371232 | CCAAGAAAGAAAGAA[C/T]TCCAGGATCCTTGGG | 7011 |
rs754263215 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408053 | AGATATCTGTAGACT[C/G]TGGAACAAGGGGCTG | 7011 |
rs754265798 | snp | C/T | 0.000164997 | 0.00908138 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382021 | CCCTTCGGTAGTGTC[C/T]GCCACACACTCAGCA | 7011 |
rs754270357 | snp | C/G | 3.33929e-05 | 0.00408599 | intron-variant | TEP1 | GRCh38.p7 | 14:20389769 | AGGGAGAAGATGCTA[C/G]AGAAGGGATGCTAGA | 7011 |
rs754317520 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372825 | AAAGGTGTGTGCCGA[A/G]GACCAGATCAGAGCA | 7011 |
rs754326450 | in-del | -/ACACACACAC | 2.06035e-05 | 0.00320957 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20368795 | CACACACACACACTT[-/ACACACACAC]ACCAGCTGCATACTG | 7011 |
rs754349221 | snp | A/G/T | 4.94355e-05 | 0.00497149 | stop-gained, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386120 | GTAGCTGGGGGGAAT[A/G/T]TATCCATAACGGGAG | 7011 |
rs754364692 | snp | C/G | 1.65021e-05 | 0.00287241 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403878 | TCTTATCTCCCTCAG[C/G]CAGGCTCTGTCAAAG | 7011 |
rs754374075 | snp | C/T | 0.000214736 | 0.0103596 | intron-variant | TEP1 | GRCh38.p7 | 14:20382213 | CCAACCAACCCACCC[C/T]AAGCACTGACCACTC | 7011 |
rs754396130 | snp | C/T | 4.97607e-05 | 0.00498777 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377725 | AGGTGCCCACGGGGC[C/T]GACCCAGAGACCCTG | 7011 |
rs754402128 | snp | A/G | 1.64749e-05 | 0.00287005 | intron-variant | TEP1 | GRCh38.p7 | 14:20386218 | CATGATGATAGGGAC[A/G]TGTGGGAGTCACTGG | 7011 |
rs754442436 | snp | C/T | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414112 | GAGACAAGTGACCCT[C/T]AGGTTAATAATCCTA | 7011 |
rs754444773 | snp | A/G | 6.60186e-05 | 0.00574499 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379057 | TATCATCGGAGAGGA[A/G]CAAACAAGCAGAGAT | 7011 |
rs754457404 | snp | A/C/T | 8.23613e-05 | 0.00641675 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408150 | GGGTGGGCAGAAACA[A/C/T]GTCCATGTGGTTTCT | 7011 |
rs754468380 | snp | G/T | 1.64795e-05 | 0.00287045 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403337 | TTAGTCCAGAAGAGA[G/T]TGTACATGCACATAT | 7011 |
rs754475543 | in-del | -/C | 0.000305821 | 0.0123619 | intron-variant | TEP1 | GRCh38.p7 | 14:20382114 | CATACGGTGTCCCCG[-/C]CCCCACCACACCCAG | 7011 |
rs754492413 | snp | G/T | 3.3162e-05 | 0.00407184 | intron-variant | TEP1 | GRCh38.p7 | 14:20390630 | TGAAATATATCAGTT[G/T]CAGAGGAAAATGTGG | 7011 |
rs754495676 | snp | C/T | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377678 | CTGGGCTGAGTGCCA[C/T]AGAGAGGGCAGGAGA | 7011 |
rs754531553 | snp | G/T | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415420 | TACGCATAAAATGCC[G/T]TGTGTTTATATTTAA | 7011 |
rs754552198 | snp | A/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371252 | GGATCCTTGGGCTGC[A/T]GGACAAATATGCCAT | 7011 |
rs754568121 | snp | C/T | 5.02391e-05 | 0.00501169 | intron-variant | TEP1 | GRCh38.p7 | 14:20379127 | CAGTGGGTGAGGGAG[C/T]GCAGCTCAGGCCATC | 7011 |
rs754589203 | snp | C/T | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368466 | GAAAGTACACATTGC[C/T]CTGCACGTCTCCCAC | 7011 |
rs754602728 | snp | A/G | 1.65075e-05 | 0.00287289 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373759 | GCTCCACGCCTTGAT[A/G]GTCCCACACTTTCAA | 7011 |
rs754606129 | snp | A/C/G | 3.29458e-05 | 0.00405857 | missense, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408196 | CAGAAAGTGTGGCCA[A/C/G]GCACTGGTTCTCCAA | 7011 |
rs754621393 | snp | A/G | 1.67335e-05 | 0.00289248 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377746 | AGAGACCCTGACCAC[A/G]CCTGAACCTGGGAAC | 7011 |
rs754639134 | snp | A/G | 1.74199e-05 | 0.00295121 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374444 | CACAGCTGCCACAGC[A/G]CTCACAGCACTCTGA | 7011 |
rs754642322 | snp | A/G | 0.000115776 | 0.00760754 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368407 | GCATCTCTAGCACAA[A/G]GGGTATCATTATTCC | 7011 |
rs754687355 | snp | C/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390718 | GACAGCAGGTATTTC[C/G]CAAAAGTATTCAGGG | 7011 |
rs754696541 | snp | A/G | 1.65326e-05 | 0.00287507 | intron-variant | TEP1 | GRCh38.p7 | 14:20403902 | GTCAAAGAGAGAGGA[A/G]AGACCACTAGAAGCA | 7011 |
rs754702761 | in-del | -/C | 1.65138e-05 | 0.00287343 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378179 | GGCCCACAGCCACAA[-/C]CCCCCCAGGCACATT | 7011 |
rs754740004 | snp | C/T | 3.32901e-05 | 0.0040797 | intron-variant | TEP1 | GRCh38.p7 | 14:20405424 | TACCAGCTTCACACC[C/T]CCATCCCCTCCTTCA | 7011 |
rs754742675 | snp | A/G | 1.64784e-05 | 0.00287035 | intron-variant | TEP1 | GRCh38.p7 | 14:20382583 | GCTGAAGAGAGAATG[A/G]GAAGTAGTGATTAGG | 7011 |
rs754746846 | snp | C/T | 1.69395e-05 | 0.00291024 | intron-variant | TEP1 | GRCh38.p7 | 14:20391583 | ACCCCTTGGAGGATG[C/T]TTTTTGTTTTCTTAC | 7011 |
rs754776716 | snp | C/T | 3.61376e-05 | 0.00425059 | intron-variant | TEP1 | GRCh38.p7 | 14:20384003 | AGCCCACACAGCCTT[C/T]CCTCCCTCCTGCCCA | 7011 |
rs754790377 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406770 | ATCCCCCAGCAGCCT[G/T]GGGCTGCTTAACCTC | 7011 |
rs754821336 | snp | A/C | 6.2115e-05 | 0.00557258 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386620 | AAGCCGGATGCTGCG[A/C]CATCTGGGGATAAGC | 7011 |
rs754834071 | snp | A/G | 1.64912e-05 | 0.00287147 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381373 | GAAGGTGCCTGAGGC[A/G]TCAGCGTCACATGTC | 7011 |
rs754839281 | snp | A/G | 1.69657e-05 | 0.00291248 | intron-variant | TEP1 | GRCh38.p7 | 14:20376269 | TGTGAAATCCTCTGC[A/G]TTGGAAAAAGAGAGA | 7011 |
rs754842310 | snp | C/T | | | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365361 | TCACTGCAACCTCTG[C/T]CCCCTGAGTTCAAGC | 7011 |
rs754854724 | snp | C/T | 1.65072e-05 | 0.00287286 | intron-variant | TEP1 | GRCh38.p7 | 14:20381446 | GCCCTGCATCATTCC[C/T]AAGGGCAGTAGGTGA | 7011 |
rs754858698 | snp | C/T | 1.65307e-05 | 0.0028749 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376180 | GGGCCCTCATGTCCC[C/T]GCAGCTCAGTGCCAC | 7011 |
rs754858941 | in-del | -/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20369011 | CTCCCTTAGTATTTC[-/T]TTTTTTTTTTTTTGA | 7011 |
rs754865736 | snp | G/T | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405514 | AAAAATGGCAGCCAG[G/T]GTGGGGTCAGATGTA | 7011 |
rs754889407 | snp | C/T | 3.37929e-05 | 0.00411039 | intron-variant | TEP1 | GRCh38.p7 | 14:20369818 | TTTAGCCTACCCATA[C/T]GAGTCAACTTGTACC | 7011 |
rs754959925 | in-del | -/T | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413870 | GTCAGACTCAATTCA[-/T]CCTAAAGTTCCTTTG | 7011 |
rs754974098 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373348 | CTGAGGTTTCTGAAA[C/T]AGCAGCAGCACGGAC | 7011 |
rs754980670 | snp | A/G | 1.64906e-05 | 0.00287142 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403734 | TGACTGGAGAGCGGG[A/G]TGGCCGGCGGGGGTG | 7011 |
rs754982820 | snp | G/T | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407958 | AGTCCCTTAGAGAAA[G/T]GCTGAGCCCTCCAAC | 7011 |
rs755018606 | snp | C/T | 1.64871e-05 | 0.00287111 | intron-variant | TEP1 | GRCh38.p7 | 14:20387896 | AAAGGCATAGAAACA[C/T]AGACTGACCCTTGCT | 7011 |
rs755019027 | snp | C/T | 1.6691e-05 | 0.00288881 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371621 | TCCTGTAGAATTCGG[C/T]TCAGGTGAAGACTAG | 7011 |
rs755019563 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411100 | GCTAGGATTACAGGC[C/G]TGAGCCACCGCACCC | 7011 |
rs755022287 | snp | A/C | 1.64773e-05 | 0.00287026 | intron-variant | TEP1 | GRCh38.p7 | 14:20384562 | CGGCTCCTCTCACCA[A/C]ATCTCTGTACAGGTG | 7011 |
rs755023811 | snp | A/G | 1.65688e-05 | 0.00287821 | intron-variant | TEP1 | GRCh38.p7 | 14:20385146 | TGAGTTTAGTCCTAG[A/G]CCACAATGACCCTCC | 7011 |
rs755075933 | snp | C/T | 0.000148541 | 0.00861674 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381942 | GACGAGGCAGGCAAA[C/T]GGGCCCATGGGGTAG | 7011 |
rs755087273 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388367 | AAAGCCATCCCAGTC[C/T]GGGCTTGAGCAGCTC | 7011 |
rs755124344 | snp | C/T | 1.66843e-05 | 0.00288823 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368840 | CTTAACATCTCTGTC[C/T]TTCGAAGCTGTCACC | 7011 |
rs755127704 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20401395 | CTGGGATGGGGGCCA[C/T]GGATGTTGAAAAGTT | 7011 |
rs755138334 | snp | C/G | 1.66371e-05 | 0.00288414 | intron-variant | TEP1 | GRCh38.p7 | 14:20395982 | GAGGGGTCATGAGCA[C/G]AGGAGCCGGGAGTAT | 7011 |
rs755151280 | snp | C/T | 5.12238e-05 | 0.00506056 | intron-variant | TEP1 | GRCh38.p7 | 14:20380184 | CAGTTTCAGAAAGAG[C/T]TGCAGCTTGCTCTCT | 7011 |
rs755156058 | in-del | -/CCCT | 1.65664e-05 | 0.00287801 | intron-variant | TEP1 | GRCh38.p7 | 14:20406212 | CCATTATTAACCTTC[-/CCCT]AACTCTTGAATTTTT | 7011 |
rs755178606 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403773 | CCCGGTGCTTCCGAG[A/G]GTTGTACTTAGCCAG | 7011 |
rs755204312 | snp | C/G | 3.30006e-05 | 0.00406192 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378156 | CAGCTCCACCATACT[C/G]TCCAGCCGGCCCACA | 7011 |
rs755207979 | snp | G/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391042 | GCACGACGTCCACCT[G/T]CTCCGCCCTCGTGAT | 7011 |
rs755222041 | snp | A/C/G | 5.79551e-05 | 0.00538282 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383852 | GACGAGCCCCAGAAA[A/C/G]GTGGAAGAAGACTAA | 7011 |
rs755232578 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20407290 | AACTGACTCTGCTAT[-/A]AGTAACATTAAGCTG | 7011 |
rs755234433 | snp | C/T | 3.29957e-05 | 0.00406162 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401109 | GGCCCAGGAAGGCGA[C/T]TTCGAGAAAAGAGCT | 7011 |
rs755249888 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20389855 | TGAGAGGAGTACCTC[A/T]CCTGAGAGCACATAG | 7011 |
rs755257631 | snp | C/T | 1.65149e-05 | 0.00287353 | intron-variant | TEP1 | GRCh38.p7 | 14:20378242 | CCCCCAGGTCCTACA[C/T]AGGGAGGTAGAAATG | 7011 |
rs755280041 | snp | A/G | 1.81283e-05 | 0.00301061 | intron-variant | TEP1 | GRCh38.p7 | 14:20408483 | AAGGAGAGAAAGACA[A/G]GAGATGAGCACCTGG | 7011 |
rs755289769 | snp | C/T | 1.64931e-05 | 0.00287163 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381016 | GTTGGTAAGGAACTT[C/T]GAAAGAAGTCCACGG | 7011 |
rs755344910 | snp | C/T | 3.30066e-05 | 0.00406229 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378790 | CACGGTGGCTAGCAG[C/T]CGGCAGTCTGGGCTC | 7011 |
rs755375798 | snp | A/T | 1.76974e-05 | 0.00297462 | intron-variant | TEP1 | GRCh38.p7 | 14:20381735 | GAAGAGGCCTGTCAG[A/T]GAGCTTCCTGGCACA | 7011 |
rs755432355 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409381 | TACTTTCCTGGAGTG[A/G]TCTCACCCACTATGT | 7011 |
rs755436356 | snp | A/G | 3.29761e-05 | 0.00406041 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377449 | TAGCCAGGCCAGGGC[A/G]GACACTGCCACATCC | 7011 |
rs755444050 | snp | C/T | 1.75659e-05 | 0.00296355 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383280 | CCCAAGGCCAGCACG[C/T]GGGCACCCTGGCTCT | 7011 |
rs755459643 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20379850 | AGAGTGATAACAGGT[A/G]TGTTTGGCTCATCTA | 7011 |
rs755464036 | snp | G/T | 1.64844e-05 | 0.00287087 | intron-variant | TEP1 | GRCh38.p7 | 14:20373168 | GGAGAAAGGACGTGT[G/T]TCATTAGGAGCTGGG | 7011 |
rs755464199 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369551 | CCATAGGATCCCATC[A/G]GAGCTGGCACACAAA | 7011 |
rs755478098 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20380895 | ACCCAGGAGTCCCAT[A/G]TCTCAGAGAAGAACC | 7011 |
rs755487709 | snp | C/T | 1.64895e-05 | 0.00287132 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373700 | GGGCTCCATGGCAGC[C/T]GCACAGTGGCTAATG | 7011 |
rs755497785 | snp | A/G | 1.8026e-05 | 0.00300211 | intron-variant | TEP1 | GRCh38.p7 | 14:20407839 | GCATACAACAGACAT[A/G]GCTGGAGTCAAGATG | 7011 |
rs755527252 | snp | C/G | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390739 | GTATTCAGGGACCAT[C/G]CATCATTTTCATCAA | 7011 |
rs755532321 | snp | A/C | 0.000150342 | 0.00866882 | intron-variant | TEP1 | GRCh38.p7 | 14:20391814 | TCAGGGACTTATCTG[A/C]CCCTTAGAGGCAGAC | 7011 |
rs755533212 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367891 | TGGGATTACAAGCGT[A/G]AGCCACCATGCCCGG | 7011 |
rs755559152 | snp | A/G | 1.64871e-05 | 0.00287111 | intron-variant | TEP1 | GRCh38.p7 | 14:20369652 | ATCTCCCGGCTCCTC[A/G]GGTCCTCCTGTTACC | 7011 |
rs755585539 | snp | G/T | 1.6777e-05 | 0.00289624 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395458 | TACATACCTGGCCTT[G/T]TGTACTCTCAGCTTC | 7011 |
rs755591950 | snp | C/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408215 | CTGGTTCTCCAAGGA[C/G]AGGATGTCTGGGTGG | 7011 |
rs755614059 | snp | A/G | 3.32094e-05 | 0.00407475 | intron-variant | TEP1 | GRCh38.p7 | 14:20395849 | GGAGTTGGAAGAAAG[A/G]GGAGAATACCTTGAT | 7011 |
rs755703673 | snp | A/G | 8.24491e-05 | 0.0064201 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385088 | TCTCTGTCACAGAGC[A/G]CCCTGAAGGGTACTG | 7011 |
rs755713258 | snp | A/T | 1.65119e-05 | 0.00287327 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382251 | CTTCTAGGGCAGTCA[A/T]GGCCTGGGGAAGGAC | 7011 |
rs755732479 | snp | C/G | 9.88403e-05 | 0.00702925 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408283 | GGTCAGGAAGCGTGG[C/G]TAGGCACTGGTTCTT | 7011 |
rs755738649 | snp | C/G | 1.65206e-05 | 0.00287403 | intron-variant | TEP1 | GRCh38.p7 | 14:20380923 | ACCCAGCCAGTGACT[C/G]ATCTCACCATAGAGG | 7011 |
rs755745149 | snp | A/G | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413845 | CCTCTCCTTCCTAAT[A/G]TCAAAGACGGTCAGA | 7011 |
rs755747395 | snp | A/G | 3.40715e-05 | 0.0041273 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404747 | ACATTCCGGACGTTC[A/G]GCTGCTGCCTGGCAT | 7011 |
rs755759342 | snp | C/G | 1.67851e-05 | 0.00289694 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375766 | TCACCAGTAGGTTAT[C/G]TTTGGTCCAGGCACA | 7011 |
rs755771378 | in-del | -/C | 1.67478e-05 | 0.00289372 | intron-variant | TEP1 | GRCh38.p7 | 14:20384284 | ATGCTCCTCAGCACT[-/C]CCAGGCTAAAACTCA | 7011 |
rs755774643 | snp | A/G | 3.32646e-05 | 0.00407814 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382303 | CAGTGTGCTCAGGAT[A/G]TGCTGCAGCAGCAGG | 7011 |
rs755784368 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20382519 | GCGAGGATAGGGAGT[A/G]GGTGATCACAAGACA | 7011 |
rs755785677 | snp | C/T | 3.30595e-05 | 0.00406554 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404687 | CGTCGCAGGTGGGGG[C/T]GACACGCCGGCAAGA | 7011 |
rs755791552 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20371837 | GCTCAAACTAGGAAT[C/T]TCTAACATTCTTGGC | 7011 |
rs755807550 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373097 | TGGAACCATCTGGTG[C/T]CCAAGCCACAGCAGT | 7011 |
rs755840652 | in-del | -/AG | 1.81238e-05 | 0.00301025 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368888 | ATGGAGGGCTGTGAC[-/AG]AGCCCGAGTGAATCT | 7011 |
rs755864874 | snp | A/G | 9.89218e-05 | 0.00703215 | intron-variant | TEP1 | GRCh38.p7 | 14:20372970 | ATACACAGCCAGGGT[A/G]GAATTCACACAGACA | 7011 |
rs755874453 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20388001 | GGTGGTGGAATCTTG[A/G]ATATTTTGTCCATTT | 7011 |
rs755877374 | snp | C/G/T | 8.23681e-05 | 0.00641702 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401013 | CAGACCGACGCTTTG[C/G/T]TCCCCCGTAGGCTCA | 7011 |
rs755897182 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387915 | CTGACCCTTGCTGGG[A/G]AACAGGAGCCAAGGG | 7011 |
rs755916357 | snp | C/G/T | 4.95522e-05 | 0.00497736 | intron-variant | TEP1 | GRCh38.p7 | 14:20406219 | TAACCTTCCCCTAAC[C/G/T]CTTGAATTTTTACCT | 7011 |
rs755916734 | snp | C/T | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414169 | GTAGCAGGAGAAATA[C/T]GCTTTCTGCCTTTAT | 7011 |
rs755918126 | snp | A/G | 1.64852e-05 | 0.00287094 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401556 | GGATTCTTTTTCTCT[A/G]ACACTGTATCACCGG | 7011 |
rs755927672 | snp | G/T | 1.65682e-05 | 0.00287817 | intron-variant | TEP1 | GRCh38.p7 | 14:20382723 | AGTCGCATCTGGCAA[G/T]ACTCAGGACTCAGGG | 7011 |
rs755939283 | snp | G/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381628 | CTGCTGTTCTCAGGG[G/T]CCCATCAGGGAGGCA | 7011 |
rs755961646 | in-del | -/A | 3.2962e-05 | 0.00405954 | intron-variant | TEP1 | GRCh38.p7 | 14:20372907 | GATGAGCCAGGATGC[-/A]CCATCTTTTCCCTCC | 7011 |
rs755974681 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376720 | CAGCAAAGTCTCCCA[C/T]GGGGCAGAAACTCAA | 7011 |
rs755976998 | snp | A/T | 6.59055e-05 | 0.00574007 | intron-variant | TEP1 | GRCh38.p7 | 14:20371438 | AGGATAACCACTAAC[A/T]CAGGTTTCCTTTTTC | 7011 |
rs755979196 | snp | A/G | 6.59e-05 | 0.00573983 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373546 | GGCCCCATCTAGCCC[A/G]ACGGTTACCACCAGA | 7011 |
rs755994322 | snp | C/T | 1.68701e-05 | 0.00290427 | intron-variant | TEP1 | GRCh38.p7 | 14:20379146 | GCTCAGGCCATCCCC[C/T]TGACCCTCCAAGTCC | 7011 |
rs756009645 | snp | A/G | 1.70734e-05 | 0.00292172 | intron-variant | TEP1 | GRCh38.p7 | 14:20377766 | AACCTGGGAACCAAG[A/G]AAAGGGCTTAAGGAT | 7011 |
rs756035803 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20395359 | CAAGCAAACCTTTAC[A/G]GAAAAACAGTTGGGA | 7011 |
rs756045751 | snp | C/T | 0.00018258 | 0.00955284 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379951 | AGTTCTCAGGTCCAA[C/T]AGGTAAACTGTCCCA | 7011 |
rs756071201 | snp | C/T | 3.39023e-05 | 0.00411704 | intron-variant | TEP1 | GRCh38.p7 | 14:20384747 | AAAAGTTGGAATAGA[C/T]TCAGACCCCAGCCAG | 7011 |
rs756084542 | snp | C/T | 1.64844e-05 | 0.00287087 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403862 | AGGGGCACCAGCTTA[C/T]TCTTATCTCCCTCAG | 7011 |
rs756103661 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371269 | GACAAATATGCCATA[C/T]TCCTTGTGGGTGGAC | 7011 |
rs756119556 | snp | A/C | 1.64765e-05 | 0.00287019 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403360 | GCACATATACAACCC[A/C]AGAAGAAGGGACTCA | 7011 |
rs756124966 | snp | A/G | 1.7598e-05 | 0.00296626 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396624 | CCTCACACATACCGC[A/G]TGCTGGAGTCTCTGG | 7011 |
rs756167603 | snp | C/T | 3.5966e-05 | 0.00424049 | intron-variant | TEP1 | GRCh38.p7 | 14:20384012 | AGCCTTCCCTCCCTC[C/T]TGCCCAGGCCCCTGA | 7011 |
rs756183086 | snp | C/T | 1.7461e-05 | 0.00295469 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383611 | CTCAGCAGACTTGGG[C/T]AGCAGCCTCTGCTGC | 7011 |
rs756185396 | snp | A/C | 1.92513e-05 | 0.00310246 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383858 | CCCCAGAAAAGTGGA[A/C]GAAGACTAATGATGC | 7011 |
rs756196263 | snp | C/T | 3.29554e-05 | 0.00405914 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380406 | ATTGAAGCCTGCTGC[C/T]TCAGGAAGGTGCGAA | 7011 |
rs756229860 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386116 | GGTTGTAGCTGGGGG[A/G]AATGTATCCATAACG | 7011 |
rs756255301 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398802 | ATCAGCAGCTTCATC[A/C]GGTAAATGCTGCTCC | 7011 |
rs756287609 | snp | A/G | 3.34163e-05 | 0.00408742 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368850 | CTGTCCTTCGAAGCT[A/G]TCACCAGCAACTCAG | 7011 |
rs756294877 | snp | C/G/T | 3.29518e-05 | 0.00405894 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369364 | TACGCTGCCGTGTCT[C/G/T]TAGATGTGGTGTTGG | 7011 |
rs756311486 | snp | A/C | 1.65173e-05 | 0.00287374 | intron-variant | TEP1 | GRCh38.p7 | 14:20378253 | TACACAGGGAGGTAG[A/C]AATGGAAACGTGAAG | 7011 |
rs756321549 | snp | A/G | 1.66946e-05 | 0.00288912 | intron-variant | TEP1 | GRCh38.p7 | 14:20391103 | CAGCGGGGGCTGATT[A/G]GACAAGTGTCAGGGG | 7011 |
rs756362969 | snp | A/C | 1.65526e-05 | 0.00287681 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376208 | CACAGGGAAAGTCTT[A/C]TGCCTTGTGTGGCCG | 7011 |
rs756394756 | snp | A/T | 1.65833e-05 | 0.00287948 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395474 | TGTACTCTCAGCTTC[A/T]CCCTCTTGAGCTGCT | 7011 |
rs756406981 | snp | C/T | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415155 | TTTGTGTATAACATT[C/T]AAGAAGACACAATGT | 7011 |
rs756415825 | snp | A/G | 1.70988e-05 | 0.00292389 | intron-variant | TEP1 | GRCh38.p7 | 14:20376276 | TCCTCTGCATTGGAA[A/G]AAGAGAGAGGGAACA | 7011 |
rs756428313 | in-del | -/CACAGCAGGTATCCA | 1.66824e-05 | 0.00288806 | intron-variant | TEP1 | GRCh38.p7 | 14:20406426 | GTGGCAGTTATGAAT[-/CACAGCAGGTATCCA]CACAGCAGGTATCCA | 7011 |
rs756452134 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant | TEP1 | GRCh38.p7 | 14:20384540 | CACAACCAGGTCAGA[A/G]CAGGCCCGGCTCCTC | 7011 |
rs756452203 | snp | C/T | 1.77203e-05 | 0.00297655 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383289 | AGCACGTGGGCACCC[C/T]GGCTCTGCTCAAGGG | 7011 |
rs756455948 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409743 | AGAAAAATGCTGGCC[A/G]GGCGCGGTGGCTCAC | 7011 |
rs756462181 | snp | A/G | 1.64977e-05 | 0.00287203 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381954 | AAACGGGCCCATGGG[A/G]TAGGGGTCTCCACTG | 7011 |
rs756468950 | in-del | -/A/C | 1.64985e-05 | 0.0028721 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380005 | TGCCCATTGGTGGAG[-/A/C]AAGGCCACAGCAGTA | 7011 |
rs756490360 | snp | C/T | 1.64876e-05 | 0.00287116 | intron-variant | TEP1 | GRCh38.p7 | 14:20377558 | GGCAGGGGCTGCGCT[C/T]TTTCTAAAGGCTCAA | 7011 |
rs756520177 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402447 | GTTTTTTCTTATAAC[A/G]CTAATATATATTTTC | 7011 |
rs756543931 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20373818 | TGCTCCTCCTGCCCA[C/T]AGAGCACAAGATCAG | 7011 |
rs756550746 | snp | G/T | 3.30453e-05 | 0.00406467 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389613 | AAGCACCCTTACAGG[G/T]ATTGTACCCTTCTTA | 7011 |
rs756583921 | snp | A/G | 1.64988e-05 | 0.00287213 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382015 | TTAGTCCCCTTCGGT[A/G]GTGTCCGCCACACAC | 7011 |
rs756595393 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372743 | TTCACCTCAAATTTC[C/T]GGGTGCCGAACCCTT | 7011 |
rs756608065 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20403596 | GCCCATGAGCTCTAC[C/G]CAGCTCCCCTGCATT | 7011 |
rs756614889 | snp | C/T | 1.64789e-05 | 0.0028704 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407969 | GAAATGCTGAGCCCT[C/T]CAACTTGGAGGCTCA | 7011 |
rs756656918 | in-del | -/CGCA | 0.000559101 | 0.0167104 | intron-variant | TEP1 | GRCh38.p7 | 14:20368759 | GGATAGGTGTGCAGG[-/CGCA]CGCACACACACACAC | 7011 |
rs756659720 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373109 | GTGCCCAAGCCACAG[C/T]AGTGACGGCTGCAGA | 7011 |
rs756662338 | snp | C/T | 2.05379e-05 | 0.00320445 | intron-variant | TEP1 | GRCh38.p7 | 14:20374400 | GCCCTTCCAGAGACC[C/T]CCCAGTGGGATCTCC | 7011 |
rs756662494 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20379799 | TGGCCAAGCCCTTTG[A/G]GCTGATGTGCAGGCA | 7011 |
rs756710868 | snp | A/G | 1.69298e-05 | 0.0029094 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382328 | AGCAGGGGGACAGTG[A/G]CAGGCAGGGTCCGGA | 7011 |
rs756741078 | snp | C/G | 6.78104e-05 | 0.00582242 | intron-variant | TEP1 | GRCh38.p7 | 14:20386025 | TTCTCCCAGCCTCTG[C/G]CCCAATCTTTGCTTC | 7011 |
rs756742930 | snp | A/C | 3.32309e-05 | 0.00407607 | intron-variant | TEP1 | GRCh38.p7 | 14:20389748 | CTGTCCACCTGTAAG[A/C]TGAAAAGGGAGAAGA | 7011 |
rs756750789 | snp | C/G/T | 6.58983e-05 | 0.00573981 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391030 | CACCTCCACACAGCA[C/G/T]GACGTCCACCTGCTC | 7011 |
rs756821811 | snp | A/G | 1.68701e-05 | 0.00290427 | intron-variant | TEP1 | GRCh38.p7 | 14:20376073 | CTAGAGAGGCTATGG[A/G]ACCCCAGGGTTGCAT | 7011 |
rs756821941 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20395109 | AAACAAACATGTCAC[A/T]GAAAAGAAAAAGAAA | 7011 |
rs756832121 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20396033 | TCTATTAGCTTTGTG[A/G]GAAGGTACAGAAGGA | 7011 |
rs756901657 | snp | A/C | 3.3479e-05 | 0.00409125 | intron-variant | TEP1 | GRCh38.p7 | 14:20405400 | CACACCATAACCACA[A/C]TCCCAGTCTACCAGC | 7011 |
rs756908200 | snp | A/C | 1.64784e-05 | 0.00287035 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20369673 | TCCTGTTACCACTCA[A/C]CAGATTCAGGTTTGG | 7011 |
rs756909135 | snp | A/G | 1.9316e-05 | 0.00310767 | intron-variant | TEP1 | GRCh38.p7 | 14:20401189 | CAGAGTCAGCAAGAA[A/G]ATAACTCAGAAAAGG | 7011 |
rs756923725 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20383404 | AGAAAAGGAGAACCA[C/T]ATTGGAGAGGCCTCT | 7011 |
rs756934390 | snp | A/G | 1.65181e-05 | 0.00287381 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401116 | GAAGGCGACTTCGAG[A/G]AAAGAGCTGTAGGTT | 7011 |
rs756934772 | snp | C/G/T | 9.89746e-05 | 0.0070341 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377471 | GCCACATCCAGTGCC[C/G/T]GACCCTGAGCCCCCT | 7011 |
rs756961191 | snp | A/T | 1.64885e-05 | 0.00287123 | intron-variant | TEP1 | GRCh38.p7 | 14:20373196 | GGGATACTGCTGGGA[A/T]AAGAGATATCAGGCC | 7011 |
rs756973073 | snp | A/C | 3.29489e-05 | 0.00405874 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384458 | CCAAACTCCTCCAGC[A/C]CGCCAACATAGGGCC | 7011 |
rs756973906 | snp | A/G | 1.64806e-05 | 0.00287054 | intron-variant | TEP1 | GRCh38.p7 | 14:20378894 | CTCTGGACCCTGGCC[A/G]TCAGCTCCCTCCTCA | 7011 |
rs757036808 | in-del | -/G | 0.000528829 | 0.0162522 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376165 | CTACAGCAGCTCACA[-/G]GGCCCTCATGTCCCC | 7011 |
rs757041532 | snp | C/T | 6.59033e-05 | 0.00573997 | intron-variant | TEP1 | GRCh38.p7 | 14:20371460 | TCCTTTTTCCCCAGC[C/T]CAGGAGGAAATGGCA | 7011 |
rs757046965 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20384943 | ACTGGCCTGTCTGGC[C/G]TTTTGGGGAAGGAGC | 7011 |
rs757047486 | snp | A/C | 0.000115358 | 0.0075938 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403465 | TGTAGGGACAGGAGA[A/C]GCAATTTCAAAAAAA | 7011 |
rs757066924 | snp | C/T | 1.65018e-05 | 0.00287239 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385019 | GGAAGTAGATGAGAG[C/T]TTGGGCAGAGGGCTG | 7011 |
rs757067361 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376040 | CAATGGGAAATGGGT[C/T]GTTAAGAAATCTAGG | 7011 |
rs757100629 | snp | A/C/T | 4.10149e-05 | 0.00452837 | intron-variant | TEP1 | GRCh38.p7 | 14:20383702 | AAAGCAGGGGTGGTA[A/C/T]GTGGGCATCAACAAG | 7011 |
rs757119391 | in-del | -/ACTCCTTGGTAT | 1.6477e-05 | 0.00287024 | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373125 | AGTGACGGCTGCAGA[-/ACTCCTTGGTAT]ACATGTGTCATCTGG | 7011 |
rs757152844 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376343 | GCCAAAGACAGGAGC[A/G]GCCATGGGGGCTGAG | 7011 |
rs757166970 | snp | A/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408219 | TTCTCCAAGGAGAGG[A/T]TGTCTGGGTGGGCAG | 7011 |
rs757182106 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374362 | ATTAGATACTCCATG[C/T]ACCGTCTCCCAAAGC | 7011 |
rs757190914 | snp | C/T | 1.65015e-05 | 0.00287237 | intron-variant | TEP1 | GRCh38.p7 | 14:20390911 | GTCCTTCATGTATTT[C/T]TGGATGGTGGGTGTT | 7011 |
rs757193694 | snp | C/T | 3.29962e-05 | 0.00406165 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378118 | GGGAAGGCAGCCAGC[C/T]GTGCCCCTTCTCGCC | 7011 |
rs757195695 | snp | A/G | 3.34219e-05 | 0.00408777 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375799 | CAGTGACCCAGTCAC[A/G]GTGACAGGCAGGGAA | 7011 |
rs757242292 | snp | A/C | 1.64814e-05 | 0.00287061 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20400989 | GTCACTCTACCAATG[A/C]GTTCCTCCCAGACCG | 7011 |
rs757246710 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374750 | TAATGAGTATAATGA[C/T]AATGTACCTATCTGA | 7011 |
rs757247521 | snp | A/C | 1.65023e-05 | 0.00287244 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395875 | TTGATTTCTGAGTTG[A/C]GCCTCGAGGGCATCA | 7011 |
rs757280062 | snp | A/C/T | 4.95081e-05 | 0.00497514 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371595 | CCAGACTTGTCAGCA[A/C/T]CCCTAAGTCCTCCTG | 7011 |
rs757287678 | snp | G/T | 1.65162e-05 | 0.00287365 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391615 | CCTTGTGGGTTGCTC[G/T]TTGGACAGAGCCTGT | 7011 |
rs757297310 | snp | A/G | 0.000197671 | 0.00993963 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391668 | GACCAAGACAGTGCG[A/G]CCTGGCAGCAGGGGC | 7011 |
rs757300276 | snp | C/T | 1.65206e-05 | 0.00287403 | splice-acceptor-variant | TEP1 | GRCh38.p7 | 14:20395950 | GTGGATCACCGACTT[C/T]TAGAAAGCAAAGGAG | 7011 |
rs757332330 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387922 | TTGCTGGGAAACAGG[A/G]GCCAAGGGGCTTGGA | 7011 |
rs757361801 | snp | A/G/T | 3.29724e-05 | 0.00406021 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381637 | TCAGGGGCCCATCAG[A/G/T]GAGGCACAGCCGGGC | 7011 |
rs757366687 | in-del | -/ACA/ACACA/ACACACA/ACACACACA/ACACACACACA/ACACACACACACA | 0.0424133 | 0.141003 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20368797 | CACACACACACTTAC[lengthTooLong]CAGCTGCATACTGGG | 7011 |
rs757369292 | in-del | -/CACGCA | 4.96938e-05 | 0.00498442 | intron-variant | TEP1 | GRCh38.p7 | 14:20368761 | ATAGGTGTGCAGGCG[-/CACGCA]CACACACACACACAC | 7011 |
rs757371904 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408241 | GGTGGGCAGACACAT[A/G]TCCATGTGGTTTTTC | 7011 |
rs757384219 | snp | C/T | 1.67038e-05 | 0.00288992 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377303 | GAAGCCAAGAGCTCC[C/T]GGGAAGTGGCCAGTC | 7011 |
rs757392741 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406240 | ATTTTTACCTTCTTT[C/T]CCTGAAGGACATGGT | 7011 |
rs757413249 | snp | C/T | 1.7569e-05 | 0.00296381 | intron-variant | TEP1 | GRCh38.p7 | 14:20376293 | AGAGAGAGGGAACAG[C/T]TTCCTGAAAGAGGAA | 7011 |
rs757445198 | snp | C/T | 3.43974e-05 | 0.00414699 | intron-variant | TEP1 | GRCh38.p7 | 14:20382759 | TCCAGGAGGGCTGCC[C/T]GCAGCCAGCCCTCTG | 7011 |
rs757499782 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366534 | ACATAAGAGAAGACA[A/G]AAGCATGGCCTATCA | 7011 |
rs757523832 | snp | A/C | 1.67531e-05 | 0.00289418 | intron-variant | TEP1 | GRCh38.p7 | 14:20389780 | GCTAGAGAAGGGATG[A/C]TAGACAGCCCAGGAC | 7011 |
rs757524367 | snp | A/C | 8.23798e-05 | 0.00641741 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406330 | ACCTCCTCCTCCTCT[A/C]CCAAGCTCAGACTAT | 7011 |
rs757533229 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20388015 | GAATATTTTGTCCAT[C/T]TGGCCCACATGTTCC | 7011 |
rs757549404 | in-del | -/T | 1.64762e-05 | 0.00287016 | intron-variant | TEP1 | GRCh38.p7 | 14:20384561 | CGGCTCCTCTCACCA[-/T]CATCTCTGTACAGGT | 7011 |
rs757550474 | snp | G/T | 1.68125e-05 | 0.00289931 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383575 | GATGATCAGGACCTG[G/T]GTCTGGCCAGGATGC | 7011 |
rs757551036 | in-del | -/CACA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368768 | GCAGGCGCACGCACA[-/CACA]CACACACACACACAC | 7011 |
rs757570351 | snp | C/G | 4.94279e-05 | 0.00497107 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373558 | CCCGACGGTTACCAC[C/G]AGAAGCTCTGACCCA | 7011 |
rs757601501 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20370493 | CCAGAATAATGTCTA[C/G]GAGGTATGTCTGTAT | 7011 |
rs757604314 | snp | A/G | 3.30044e-05 | 0.00406216 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382022 | CCTTCGGTAGTGTCC[A/G]CCACACACTCAGCAC | 7011 |
rs757617935 | snp | A/G | 3.30879e-05 | 0.00406729 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368400 | AGGCTTTGCATCTCT[A/G]GCACAAGGGGTATCA | 7011 |
rs757623855 | snp | G/T | 3.93468e-05 | 0.0044353 | intron-variant | TEP1 | GRCh38.p7 | 14:20374408 | AGAGACCCCCCAGTG[G/T]GATCTCCATTGCTTT | 7011 |
rs757657863 | snp | C/T | 1.67607e-05 | 0.00289483 | intron-variant | TEP1 | GRCh38.p7 | 14:20382093 | TCTCTGAGGCCCTCA[C/T]CTAACCATACGGTGT | 7011 |
rs757657951 | snp | A/G | 6.58913e-05 | 0.00573945 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380313 | CTCCGGGAGAGCAGC[A/G]AGGCTTGGTGGCAAA | 7011 |
rs757662927 | in-del | -/AGA | | | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367560 | GAAGTTGGGAAAACC[-/AGA]AGGTTTGTTCCGCTT | 7011 |
rs757676199 | in-del | -/GTGT | 1.67674e-05 | 0.00289541 | intron-variant | TEP1 | GRCh38.p7 | 14:20391109 | GGGCTGATTGGACAA[-/GTGT]CAGGGGAAATAAAGC | 7011 |
rs757688772 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20412352 | GTGAGACTGTCCTAT[C/G]CTTAAAAGGACAGTC | 7011 |
rs757707223 | snp | C/G | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413654 | TGGGGCCCGAGTTTA[C/G]TTTGTTATTGTTTCT | 7011 |
rs757731695 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20390787 | ACTTCATGTTATGTG[A/G]TTGCACAGTAAGCGA | 7011 |
rs757734167 | snp | A/G | 4.94205e-05 | 0.0049707 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372826 | AAGGTGTGTGCCGAG[A/G]ACCAGATCAGAGCAC | 7011 |
rs757735496 | snp | A/C/T | 0.00011928 | 0.00772189 | intron-variant | TEP1 | GRCh38.p7 | 14:20368947 | TGAGTTCTCAGGGGC[A/C/T]CCTCCTCAGAGAAGC | 7011 |
rs757753303 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374533 | CATCACTGGAGCAGG[A/G]TATCTACAGAGTCAG | 7011 |
rs757759281 | snp | G/T | 4.94344e-05 | 0.00497139 | intron-variant | TEP1 | GRCh38.p7 | 14:20372884 | AACAAGTTCAATTCA[G/T]TGCTTCTGATGAGCC | 7011 |
rs757777095 | snp | C/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369688 | CCAGATTCAGGTTTG[C/G]CTTGAGTTATCGATA | 7011 |
rs757784132 | snp | A/T | 4.94385e-05 | 0.0049716 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378408 | AGCCCATCCACCTGG[A/T]AGAAGCTGATGCTGC | 7011 |
rs757835545 | snp | C/T | 1.65754e-05 | 0.00287879 | intron-variant | TEP1 | GRCh38.p7 | 14:20401431 | ATTACTTAGATGGAA[C/T]GCATGCTCAGGGTGC | 7011 |
rs757847175 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366551 | AGCATGGCCTATCAG[C/T]GGATGTCATCATCCT | 7011 |
rs757853399 | snp | G/T | 9.88468e-05 | 0.00702948 | intron-variant | TEP1 | GRCh38.p7 | 14:20386222 | ATGATAGGGACGTGT[G/T]GGAGTCACTGGGGGC | 7011 |
rs757899029 | snp | C/T | 6.59511e-05 | 0.00574206 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403739 | GGAGAGCGGGGTGGC[C/T]GGCGGGGGTGTCTCT | 7011 |
rs757967279 | in-del | -/GTGG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410799 | AATTGTTTCTCCTTT[-/GTGG]TTTTTTTTTTTTTTT | 7011 |
rs757967658 | snp | C/G | 1.65034e-05 | 0.00287253 | intron-variant | TEP1 | GRCh38.p7 | 14:20381421 | ATGAACAGATATTGA[C/G]AAAGGCTCAGCCCTG | 7011 |
rs758003177 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405300 | CTTCACTGAACCACA[A/G]GGACTAGGCCGCAGA | 7011 |
rs758024202 | snp | C/T | 3.29614e-05 | 0.00405951 | intron-variant | TEP1 | GRCh38.p7 | 14:20378905 | GGCCATCAGCTCCCT[C/T]CTCATTTCCTTCTCC | 7011 |
rs758033566 | snp | A/G | 1.65157e-05 | 0.0028736 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395491 | CCTCTTGAGCTGCTC[A/G]TACAACACAGGTATC | 7011 |
rs758036278 | in-del | -/G | 1.65149e-05 | 0.00287353 | intron-variant | TEP1 | GRCh38.p7 | 14:20377540 | ACTTGGGAAGGGGTA[-/G]GGGGCAGGGGCTGCG | 7011 |
rs758079063 | snp | G/T | 1.64773e-05 | 0.00287026 | intron-variant | TEP1 | GRCh38.p7 | 14:20377593 | CCACCCATTCCCATT[G/T]CAGTACCTGAAGAGA | 7011 |
rs758090740 | snp | A/G | 1.66112e-05 | 0.00288189 | intron-variant | TEP1 | GRCh38.p7 | 14:20369790 | TGCCTCTGTGAAAGA[A/G]TAGGTAATTTTGTTT | 7011 |
rs758158774 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407989 | TTGGAGGCTCAGAGA[A/G]CAGGCAATTGCTGTT | 7011 |
rs758168780 | snp | G/T | 3.9454e-05 | 0.00444133 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383780 | CTGGCTCTTTTAGTT[G/T]GCCACGCAGATAGGT | 7011 |
rs758170545 | snp | A/G | 1.65364e-05 | 0.0028754 | intron-variant | TEP1 | GRCh38.p7 | 14:20385130 | GGGAGGACAGAGACA[A/G]TGAGTTTAGTCCTAG | 7011 |
rs758191898 | in-del | -/CACA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368765 | GTGTGCAGGCGCACG[-/CACA]CACACACACACACAC | 7011 |
rs758209798 | snp | A/G | 1.94725e-05 | 0.00312023 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383837 | CAAGACCCTGGTCAG[A/G]ACGAGCCCCAGAAAA | 7011 |
rs758233284 | snp | A/G | 8.88486e-05 | 0.00666456 | intron-variant | TEP1 | GRCh38.p7 | 14:20408468 | CTTGTATATGCCTAG[A/G]AGGAGAGAAAGACAG | 7011 |
rs758234520 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397674 | GATTTGCACTGGAGA[A/T]AGAATTTCACCACTG | 7011 |
rs758245696 | snp | A/G | 1.70845e-05 | 0.00292267 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382337 | ACAGTGGCAGGCAGG[A/G]TCCGGAGTCTCTCAG | 7011 |
rs758264887 | in-del | -/GT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400299 | TGTGTGTGGGTGCGT[-/GT]GTGTGTGTGTGTGCA | 7011 |
rs758276338 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408313 | TCAAGGAGAGGATAT[C/T]TGAGTGGGTAGATAC | 7011 |
rs758288220 | snp | A/G | 1.66574e-05 | 0.0028859 | intron-variant | TEP1 | GRCh38.p7 | 14:20405421 | GTCTACCAGCTTCAC[A/G]CCCCCATCCCCTCCT | 7011 |
rs758294206 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374125 | TAGGGTCTCACTCTG[C/T]TACACTGGAGGCTGG | 7011 |
rs758311206 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376032 | GGAGGAAGCAATGGG[-/A]AATGGGTTGTTAAGA | 7011 |
rs758322729 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398615 | TCATATGGATTCAGT[A/G]ACTATGTGGGTTCAA | 7011 |
rs758332969 | snp | G/T | 1.65362e-05 | 0.00287538 | intron-variant | TEP1 | GRCh38.p7 | 14:20368590 | AAATAGGGGAGGTCA[G/T]GGCTACAAGCCTCCT | 7011 |
rs758346602 | snp | C/T | 1.65326e-05 | 0.00287507 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376159 | CTGAAACTACAGCAG[C/T]TCACAGGGCCCTCAT | 7011 |
rs758357778 | snp | A/C | 1.65872e-05 | 0.00287981 | intron-variant | TEP1 | GRCh38.p7 | 14:20391789 | GCAAGAAAGACACAG[A/C]CACAGGGGCTCAGGG | 7011 |
rs758377272 | in-del | -/AGGGACAGTTTAGTCTCAGAACCTGGATAC | 1.76583e-05 | 0.00297134 | intron-variant | TEP1 | GRCh38.p7 | 14:20381095 | AAGGGGCTGGTGAGA[lengthTooLong]AGAGATAGGATCTGA | 7011 |
rs758378275 | snp | A/G | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415489 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGTGGGCA | 7011 |
rs758425360 | snp | C/T | 1.69614e-05 | 0.00291211 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368804 | CACACTTACCAGCTG[C/T]ATACTGGGTCTCTCC | 7011 |
rs758433832 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411725 | GCTCAATTTTCAGAG[C/T]GTCTATGAAGCCCAT | 7011 |
rs758467186 | snp | C/T | 4.94556e-05 | 0.00497246 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20388044 | CCAGAAGATGGGAGG[C/T]CCCATGCTCTGCAAT | 7011 |
rs758493257 | snp | A/G | 3.29995e-05 | 0.00406185 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380008 | CCCATTGGTGGAGAA[A/G]GCCACAGCAGTAGGG | 7011 |
rs758529558 | snp | C/T | 1.7565e-05 | 0.00296347 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383189 | CTGGTTGTTAAATGG[C/T]GACTCCTCCAGCCGC | 7011 |
rs758531179 | snp | A/C | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377437 | TACCTTGGGGCTTAG[A/C]CAGGCCAGGGCGGAC | 7011 |
rs758549508 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376823 | CAAGATAATTGCATT[C/T]AAAAGCACTTTGAAA | 7011 |
rs758565231 | snp | A/G | 1.64765e-05 | 0.00287019 | intron-variant | TEP1 | GRCh38.p7 | 14:20373612 | GAGACTGAGTCAGAA[A/G]AAGGGACGGAGCAGG | 7011 |
rs758583554 | snp | A/G | 1.74732e-05 | 0.00295572 | intron-variant | TEP1 | GRCh38.p7 | 14:20381725 | AGAGAAGAAGGAAGA[A/G]GCCTGTCAGTGAGCT | 7011 |
rs758597044 | snp | A/G | 1.64885e-05 | 0.00287123 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395881 | TCTGAGTTGAGCCTC[A/G]AGGGCATCAATGGCA | 7011 |
rs758611607 | snp | C/T | 1.80419e-05 | 0.00300344 | intron-variant | TEP1 | GRCh38.p7 | 14:20407827 | CTAGAGACAAGAGCA[C/T]ACAACAGACATGGCT | 7011 |
rs758642351 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20377883 | AGCTGCCCCTGCACA[C/G]AGCGGCACCCCTCTC | 7011 |
rs758647976 | in-del | -/C | 1.65403e-05 | 0.00287574 | intron-variant | TEP1 | GRCh38.p7 | 14:20405442 | ATCCCCTCCTTCACA[-/C]CTCAATACCTTGAGG | 7011 |
rs758662321 | snp | A/C | 9.885e-05 | 0.0070296 | intron-variant | TEP1 | GRCh38.p7 | 14:20386237 | GGGAGTCACTGGGGG[A/C]ATGGTATCAGGGAAC | 7011 |
rs758670536 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394986 | ACATCTGTCTTTGAG[A/C]CTGCTGATGGTAACT | 7011 |
rs758671489 | snp | C/T | 1.65875e-05 | 0.00287984 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371611 | CCCTAAGTCCTCCTG[C/T]AGAATTCGGTTCAGG | 7011 |
rs758674693 | snp | A/G | 3.30311e-05 | 0.0040638 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382230 | AGCACTGACCACTCC[A/G]TGTGACTTCTAGGGC | 7011 |
rs758696314 | snp | C/G | 1.64966e-05 | 0.00287194 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403727 | CAGTGACTGACTGGA[C/G]AGCGGGGTGGCCGGC | 7011 |
rs758754104 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20391569 | ATTCTACCAACCCAA[A/C]CCCTTGGAGGATGCT | 7011 |
rs758767770 | snp | A/G | 1.648e-05 | 0.0028705 | intron-variant | TEP1 | GRCh38.p7 | 14:20372905 | CTGATGAGCCAGGAT[A/G]CACCATCTTTTCCCT | 7011 |
rs758782717 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400700 | TGAGTTACAGAGATA[G/T]CGATATGAGTACAAT | 7011 |
rs758800739 | snp | C/T | 1.6989e-05 | 0.00291449 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386463 | TGTTCCTACGGGTCT[C/T]CTCCTCAGTGACGCC | 7011 |
rs758805922 | snp | A/C | 3.32939e-05 | 0.00407993 | intron-variant | TEP1 | GRCh38.p7 | 14:20380892 | CACACCCAGGAGTCC[A/C]ATATCTCAGAGAAGA | 7011 |
rs758850137 | snp | A/C | 3.29495e-05 | 0.00405877 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369388 | GTGTTGGCTCACTAT[A/C]CATGCTGGCATCACT | 7011 |
rs758858880 | snp | A/G | 1.67164e-05 | 0.00289101 | intron-variant | TEP1 | GRCh38.p7 | 14:20378553 | GAGGGAGAGAGAGGA[A/G]GAATCAGGATGCTGA | 7011 |
rs758888314 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20412157 | CTCACTGGACGTCAG[C/T]GTGACAAACACGTAA | 7011 |
rs758900357 | snp | C/T | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377382 | AGCATTCCTTGAGTG[C/T]CCAGCCCTGCAAGGA | 7011 |
rs758909212 | snp | C/T | 3.50361e-05 | 0.00418531 | intron-variant | TEP1 | GRCh38.p7 | 14:20382765 | AGGGCTGCCCGCAGC[C/T]AGCCCTCTGCCCCAG | 7011 |
rs758909688 | snp | C/T | 0.000115305 | 0.00759205 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369539 | TTTGGCCAGGTTCCA[C/T]AGGATCCCATCAGAG | 7011 |
rs758913785 | in-del | -/T | 1.65206e-05 | 0.00287403 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391765 | CCATCATATTTCCAC[-/T]GTCTACATGCAAGAA | 7011 |
rs758925232 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20365835 | TACCTCTGCTCTAGA[C/T]TTCAAAAACAGATGT | 7011 |
rs758949557 | snp | A/G | 1.66051e-05 | 0.00288137 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377321 | GAAGTGGCCAGTCCT[A/G]GCACAGGCTTCTGGA | 7011 |
rs758949801 | snp | C/G | 4.94303e-05 | 0.00497119 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391729 | GTCTCTAGGGCCTGT[C/G]GGTACCTGTTCAGCA | 7011 |
rs758954509 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20389147 | GTGAGATTCTGTCTT[-/A]AAAAAAAAAAAAAAG | 7011 |
rs758956716 | snp | C/T | 6.58979e-05 | 0.00573974 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401006 | TTCCTCCCAGACCGA[C/T]GCTTTGTTCCCCCGT | 7011 |
rs758982184 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391694 | GGGGCAGGCTGTGCT[C/T]CACAGAGAGGTTCAC | 7011 |
rs758988964 | snp | A/G | 3.32386e-05 | 0.00407654 | intron-variant | TEP1 | GRCh38.p7 | 14:20388091 | ACAAGATAAATGAGA[A/G]TAGAATACCACAGGT | 7011 |
rs759046925 | snp | C/T | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381598 | GCCCTGGCCTCTTCC[C/T]ATAGCAACGTTTAGC | 7011 |
rs759056277 | snp | C/T | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20388049 | AGATGGGAGGCCCCA[C/T]GCTCTGCAATGAACC | 7011 |
rs759092050 | snp | C/T | 1.68366e-05 | 0.00290138 | intron-variant | TEP1 | GRCh38.p7 | 14:20381694 | CTAGCAAACTGTCCT[C/T]GTGTGAGGAAGGGAG | 7011 |
rs759095068 | snp | A/G | 4.94376e-05 | 0.00497156 | intron-variant | TEP1 | GRCh38.p7 | 14:20373649 | AAGAAGAGACAGCAG[A/G]GAAGGGGAGGTGGCT | 7011 |
rs759099382 | snp | C/T | 4.94197e-05 | 0.00497066 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403422 | GTACCTTGGAAAACA[C/T]CTGTGAGAAAATGGA | 7011 |
rs759146432 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375236 | GGAGTGCAATGGCGC[A/G]ACCTCTGCCTCCCGG | 7011 |
rs759151434 | snp | A/G | 3.29462e-05 | 0.00405857 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371545 | CTTCAAATCTGCTTT[A/G]GCCAAGATGAGAAAG | 7011 |
rs759154083 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373530 | GATGCCATAACCGTG[C/T]GGCCCCATCTAGCCC | 7011 |
rs759188342 | snp | A/C | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378764 | CTTACCTTTAGGCAT[A/C]CTCCCAAGCACACGG | 7011 |
rs759192817 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405707 | AGATGTGGAGTCCAG[C/T]TGAGAACTTACAAAA | 7011 |
rs759200532 | snp | A/G | 6.59217e-05 | 0.00574078 | intron-variant | TEP1 | GRCh38.p7 | 14:20371358 | CTCAGGATTTAAAGA[A/G]AGGTAAAGAGAAGAA | 7011 |
rs759204124 | in-del | -/A | 4.06909e-05 | 0.00451041 | intron-variant | TEP1 | GRCh38.p7 | 14:20396763 | TAGAGTGAGAAAAAC[-/A]AATGAGAAGGCCAGG | 7011 |
rs759230960 | snp | C/T | 0.000117013 | 0.00764805 | intron-variant | TEP1 | GRCh38.p7 | 14:20395828 | GTCAGATGTGGGAGG[C/T]AAAGAGGAGTTGGAA | 7011 |
rs759234232 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368752 | CCCTTTGGGATAGGT[G/T]TGCAGGCGCACGCAC | 7011 |
rs759238055 | snp | C/T | 8.31069e-05 | 0.00644566 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380044 | GGAAACTGCCAGAGA[C/T]AGGCTGGAGCTAGAG | 7011 |
rs759276890 | snp | C/T | 3.31417e-05 | 0.00407059 | intron-variant | TEP1 | GRCh38.p7 | 14:20403693 | CCTGGAGAAAAGGGG[C/T]GTGGGTCGAGGGCTG | 7011 |
rs759277742 | snp | C/T | 1.65507e-05 | 0.00287664 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384101 | CCTTCCGTGGGGCAG[C/T]ATCAGCCGTTGCACT | 7011 |
rs759288111 | snp | C/G | 1.71649e-05 | 0.00292953 | intron-variant | TEP1 | GRCh38.p7 | 14:20404593 | GAAGGCCCAAGCTCA[C/G]GGAAATGAGCACCAT | 7011 |
rs759312081 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant | TEP1 | GRCh38.p7 | 14:20372867 | TGGAGCCTGGTGTAC[A/G]CAACAAGTTCAATTC | 7011 |
rs759370060 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393130 | GCTGAAGCAGGAGAA[C/T]GGTGTGAACCCAGGA | 7011 |
rs759370272 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20379378 | GGGGTAGGGGATGAC[A/G]TGAGTGTAAAGAGGA | 7011 |
rs759457098 | snp | A/C | 4.95405e-05 | 0.00497673 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384178 | GCTGCTGGAAGGTGG[A/C]CTGGACCAAGTCATC | 7011 |
rs759458718 | snp | A/G | 1.68097e-05 | 0.00289906 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380464 | TTTGTTCCTCTTTGG[A/G]GACTGAAGAAGCTAT | 7011 |
rs759460543 | snp | A/C | 1.64871e-05 | 0.00287111 | intron-variant | TEP1 | GRCh38.p7 | 14:20378375 | GCAACACTGGACCTT[A/C]TTACCTTGGTGACTT | 7011 |
rs759471372 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369491 | TTTTTTCTGCCACAT[A/G]TTACCTGTGGTCCAT | 7011 |
rs759505731 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408913 | AGGAGACCCAACCCC[C/G]CTGACCCCCGCTGCA | 7011 |
rs759511631 | snp | C/G | 1.65179e-05 | 0.00287379 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378483 | GCAACACAGTTCAGG[C/G]ACTTGGGGTAGGTGT | 7011 |
rs759562202 | in-del | -/AAGA | 1.64876e-05 | 0.00287116 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379031 | CCCGTCGAAGGCAGT[-/AAGA]AAGAGTGTATCATCG | 7011 |
rs759565225 | snp | C/T | 3.33211e-05 | 0.0040816 | intron-variant | TEP1 | GRCh38.p7 | 14:20406188 | TCCACCACCAACCTC[C/T]CCTCCACACCATTAT | 7011 |
rs759587736 | snp | C/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391656 | ATCTGTCAGATAGAC[C/G]AAGACAGTGCGGCCT | 7011 |
rs759595173 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402553 | TTTAAATATAGTAAC[-/T]TATTTAATCTTTATG | 7011 |
rs759642227 | snp | C/T | 3.2981e-05 | 0.00406071 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395531 | ATCCGAAGCTGCTGA[C/T]GGCTTAGGTGGCAAA | 7011 |
rs759647709 | snp | A/G | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373717 | CACAGTGGCTAATGG[A/G]TCCTGAGTGAGCAGG | 7011 |
rs759672567 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411936 | TGGGCAACATAGTGA[C/G]ACCTCTATTTAAAAA | 7011 |
rs759684509 | snp | C/T | 1.65488e-05 | 0.00287647 | intron-variant | TEP1 | GRCh38.p7 | 14:20382182 | CAATGTAATCCGAAC[C/T]CTGGCCCTCAGCCTC | 7011 |
rs759701461 | snp | A/G | 1.65485e-05 | 0.00287645 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389721 | TCCATGCTTTGGCCA[A/G]GGAGGATGACCCTGT | 7011 |
rs759725538 | in-del | -/CCCCAGGAAC | 0.000198268 | 0.00995463 | intron-variant | TEP1 | GRCh38.p7 | 14:20375707 | GGGAGTGTTGTCTTG[-/CCCCAGGAAC]CCAGCTGGGCTCTGT | 7011 |
rs759726973 | snp | G/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408128 | GTTCTCCAAGGAGAG[G/T]ATGTCTGGGTGGGCA | 7011 |
rs759727918 | snp | C/G | 1.65247e-05 | 0.00287438 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377709 | GAGAGAAAGGGAACC[C/G]AGGTGCCCACGGGGC | 7011 |
rs759731173 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20382988 | GAAAGGCCATTCACC[A/G]GGGGAAGAGGGCTGG | 7011 |
rs759750847 | snp | C/T | 6.65967e-05 | 0.00577009 | intron-variant | TEP1 | GRCh38.p7 | 14:20382078 | CCTGAAAACTCAAGC[C/T]CTCTGAGGCCCTCAT | 7011 |
rs759799947 | snp | A/G | 1.64732e-05 | 0.0028699 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408028 | GGTACAAATCAGCTT[A/G]CGTCATGTGAGATAT | 7011 |
rs759805286 | snp | G/T | 3.29587e-05 | 0.00405934 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403851 | GACAGGCGGGCAGGG[G/T]CACCAGCTTATTCTT | 7011 |
rs759843238 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20371157 | CATGACGGGCCCCAA[C/G]GTGTAAAAACACTGG | 7011 |
rs759869254 | snp | C/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386109 | TCAGGAAGGTTGTAG[C/G]TGGGGGGAATGTATC | 7011 |
rs759873622 | snp | G/T | 1.66034e-05 | 0.00288122 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376120 | CGATCCCGGCCCCCG[G/T]TGGCCAGGCTGCCTC | 7011 |
rs759902609 | snp | C/T | 1.65051e-05 | 0.00287267 | intron-variant | TEP1 | GRCh38.p7 | 14:20390664 | AGGGAGAGGGTTTCT[C/T]AGGGATTAATACTCA | 7011 |
rs759914003 | snp | G/T | 5.19863e-05 | 0.00509808 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386576 | AGGTCCCGCTCCCCA[G/T]GCATGTCTCGGAAAG | 7011 |
rs759914049 | snp | C/T | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391063 | CCCTCGTGATCATCA[C/T]CCCAATCAACAGCAG | 7011 |
rs759917381 | snp | A/C | 8.24994e-05 | 0.00642206 | intron-variant | TEP1 | GRCh38.p7 | 14:20381411 | GCTGAGCTGCATGAA[A/C]AGATATTGAGAAAGG | 7011 |
rs759925531 | snp | C/T | 4.94287e-05 | 0.00497111 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373378 | CTGGGCCGCTGTGTC[C/T]CAGGAGGGTGTGGGT | 7011 |
rs759929664 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410679 | ACTCCTGACCTTGTG[A/G]TCCACCCACCTTGGC | 7011 |
rs759947993 | snp | A/G | 0.000115364 | 0.00759399 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405475 | AAACTCAGGCTCCAG[A/G]AGGGCAAGTTCACGA | 7011 |
rs759970420 | snp | A/G | 3.29788e-05 | 0.00406058 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378991 | CTTACCGACAACCAT[A/G]CTGCAGGTCCCAGAG | 7011 |
rs759978070 | snp | A/T | 1.80745e-05 | 0.00300615 | intron-variant | TEP1 | GRCh38.p7 | 14:20382392 | CCTTGTTCAGTGCAG[A/T]GGGAGGAGAAGCAGC | 7011 |
rs759991930 | snp | A/G | 1.64808e-05 | 0.00287057 | intron-variant | TEP1 | GRCh38.p7 | 14:20381296 | GGGAAAGGTGTCTAT[A/G]GGGTCTAGGAACTAA | 7011 |
rs760005252 | snp | C/G | 6.59446e-05 | 0.00574177 | missense, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401470 | ACCTGTAACCCAGCA[C/G]GGCTTGAACGTGCTG | 7011 |
rs760029456 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382647 | CAGCGTGAAGAGCCT[C/T]AGGTGATCGGTGACC | 7011 |
rs760044990 | snp | G/T | 0.000131837 | 0.00811795 | intron-variant | TEP1 | GRCh38.p7 | 14:20378866 | ACCCTATCCCAGGAA[G/T]ATGAAGTCAGTCCTC | 7011 |
rs760062295 | in-del | -/C | 1.65411e-05 | 0.00287581 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20389609 | GTATAAGCACCCTTA[-/C]AGGTATTGTACCCTT | 7011 |
rs760081103 | snp | C/T | 1.65261e-05 | 0.0028745 | intron-variant | TEP1 | GRCh38.p7 | 14:20389324 | AGAAGCAGTCATTAA[C/T]CATCACAAACAATAC | 7011 |
rs760117859 | snp | C/T | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395927 | AATCTGAATGGAAAC[C/T]GCCGACTGTGGATCA | 7011 |
rs760136077 | snp | A/G | 0.000148644 | 0.00861973 | intron-variant | TEP1 | GRCh38.p7 | 14:20385114 | TACTGCTGGGCCTGC[A/G]GGGAGGACAGAGACA | 7011 |
rs760137518 | snp | C/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373296 | GGAACCTGCCAGAGC[C/T]GTACAGAACCATCCT | 7011 |
rs760201651 | snp | A/G | 0.00826489 | 0.0637506 | intron-variant | TEP1 | GRCh38.p7 | 14:20368768 | TGCAGGCGCACGCAC[A/G]CACACACACACACAC | 7011 |
rs760212620 | snp | A/G | 3.30175e-05 | 0.00406296 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385011 | GGAATCCCGGAAGTA[A/G]ATGAGAGCTTGGGCA | 7011 |
rs760223383 | snp | C/G/T | 3.3099e-05 | 0.004068 | intron-variant | TEP1 | GRCh38.p7 | 14:20403700 | AAAAGGGGCGTGGGT[C/G/T]GAGGGCTGGGGCAGT | 7011 |
rs760234839 | snp | C/G | 1.67038e-05 | 0.00288992 | intron-variant | TEP1 | GRCh38.p7 | 14:20380057 | GACAGGCTGGAGCTA[C/G]AGAAAGAGTAGGAAG | 7011 |
rs760245245 | in-del | -/AA | 7.72335e-05 | 0.00621376 | intron-variant | TEP1 | GRCh38.p7 | 14:20401191 | AGTCAGCAAGAAAAT[-/AA]AACTCAGAAAAGGAA | 7011 |
rs760254449 | snp | A/G | 1.71009e-05 | 0.00292406 | intron-variant | TEP1 | GRCh38.p7 | 14:20371648 | CTAGCTCAAAAAAGT[A/G]CATGGACAGAGAAAG | 7011 |
rs760264963 | snp | C/G | 1.70857e-05 | 0.00292276 | intron-variant | TEP1 | GRCh38.p7 | 14:20375916 | GACCAAAGGAAGGAT[C/G]GGAACCCCGGAGCCA | 7011 |
rs760287757 | snp | C/T | 1.65474e-05 | 0.00287636 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380247 | TACCTTTGCTGATTT[C/T]TCATGGTCCGGGGTT | 7011 |
rs760296382 | snp | C/G | 6.59087e-05 | 0.00574021 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371571 | GAAAGTGACCATCAG[C/G]AGCCCAATCCAGACT | 7011 |
rs760296837 | snp | A/G | 2.0112e-05 | 0.00317106 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383744 | TGGGGGATACCCACC[A/G]GTAGGTGCTGGGGAG | 7011 |
rs760301602 | snp | C/T | 0.000115316 | 0.00759243 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391020 | TTCAGAGTGTCACCT[C/T]CACACAGCACGACGT | 7011 |
rs760315262 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366335 | TTGGCCCAAGATTTT[A/T]GGGGAGCAAAAGGCA | 7011 |
rs760339144 | snp | G/T | 1.65004e-05 | 0.00287227 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378206 | CATTGAAGGCCAAGG[G/T]ACGGATAGAGGCTCC | 7011 |
rs760348279 | snp | C/T | 1.96261e-05 | 0.00313252 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383805 | ATAGGTACAGAGGCG[C/T]CTGAGCAGAGTGAGG | 7011 |
rs760377398 | snp | C/T | 4.95896e-05 | 0.00497919 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384192 | GCCTGGACCAAGTCA[C/T]CGTCTGGGATGGACA | 7011 |
rs760386417 | snp | C/G | 1.64936e-05 | 0.00287168 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368551 | CCCTTCGCATCGGAA[C/G]AGGCCCAGCTACGAT | 7011 |
rs760414472 | snp | A/C/T | 9.88442e-05 | 0.00702946 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391666 | TAGACCAAGACAGTG[A/C/T]GGCCTGGCAGCAGGG | 7011 |
rs760414666 | snp | A/C | 1.64735e-05 | 0.00286993 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401034 | CGTAGGCTCAGCTCC[A/C]GCTCCCAGGTCTCTG | 7011 |
rs760440928 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402135 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAACTA | 7011 |
rs760454927 | snp | G/T | 6.59446e-05 | 0.00574177 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390748 | GACCATCCATCATTT[G/T]CATCAAACTCCTGAA | 7011 |
rs760467813 | snp | C/T | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391748 | ACCTGTTCAGCATCT[C/T]ACCATCATATTTCCA | 7011 |
rs760549561 | snp | C/T | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391712 | CAGAGAGGTTCACAG[C/T]TGTCTCTAGGGCCTG | 7011 |
rs760555412 | snp | A/G | 1.70095e-05 | 0.00291625 | intron-variant | TEP1 | GRCh38.p7 | 14:20381701 | ACTGTCCTCGTGTGA[A/G]GAAGGGAGAGAGAAG | 7011 |
rs760587162 | snp | C/T | 4.94572e-05 | 0.00497254 | intron-variant | TEP1 | GRCh38.p7 | 14:20384343 | CAGGACAACCCAGAC[C/T]ACCCCATGTCCCTCT | 7011 |
rs760610542 | snp | G/T | 1.65091e-05 | 0.00287303 | intron-variant | TEP1 | GRCh38.p7 | 14:20369615 | GAGCCAAGTCTCAGG[G/T]ATCTGCCATCCACCC | 7011 |
rs760611738 | snp | A/T | 1.72383e-05 | 0.00293578 | intron-variant | TEP1 | GRCh38.p7 | 14:20377277 | CCCACTGTCTAGTAG[A/T]ACCTGAGGCAGAAGC | 7011 |
rs760613315 | snp | A/G | 1.69453e-05 | 0.00291073 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383240 | CTCTCTCACCAGCCG[A/G]GCCCGAGCAGAGGCC | 7011 |
rs760664726 | snp | G/T | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377391 | TGAGTGCCCAGCCCT[G/T]CAAGGACCCATCTTC | 7011 |
rs760665243 | snp | C/G | 0.000133828 | 0.00817902 | intron-variant | TEP1 | GRCh38.p7 | 14:20382089 | AAGCTCTCTGAGGCC[C/G]TCATCTAACCATACG | 7011 |
rs760685579 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406311 | CTTCACGGCCAGATC[C/T]TCCACCTCCTCCTCC | 7011 |
rs760709898 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20378950 | AATGGGGAAGGCCCT[C/T]ATTCCAAGACAAATG | 7011 |
rs760721934 | snp | A/G | 3.29669e-05 | 0.00405984 | intron-variant | TEP1 | GRCh38.p7 | 14:20373673 | GGTGGCTGACGTTTT[A/G]TTACCTGCACGGGGC | 7011 |
rs760731056 | snp | G/T | 1.65545e-05 | 0.00287697 | intron-variant | TEP1 | GRCh38.p7 | 14:20389193 | TAATCTCCTAAAAAC[G/T]TTCCAACAAAGTATC | 7011 |
rs760739657 | snp | A/G | 3.57667e-05 | 0.00422872 | intron-variant | TEP1 | GRCh38.p7 | 14:20383656 | GCTTCTGTACATGGA[A/G]AGGAAGTCAGGGTCA | 7011 |
rs760741940 | in-del | -/ATA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372073 | CTTTATAAAATCCAG[-/ATA]ATTATTCCACCCAAA | 7011 |
rs760743295 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408142 | GGATGTCTGGGTGGG[A/C]AGAAACATGTCCATG | 7011 |
rs760748568 | snp | C/T | 0.000115309 | 0.00759218 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403434 | ACATCTGTGAGAAAA[C/T]GGAGGCTCCATCCCC | 7011 |
rs760784175 | snp | A/T | 1.75372e-05 | 0.00296113 | intron-variant | TEP1 | GRCh38.p7 | 14:20395677 | GCTTCTATTCCCTCA[A/T]CTTTTCCTACCAGTA | 7011 |
rs760794673 | snp | A/C/T | 3.30503e-05 | 0.00406501 | intron-variant | TEP1 | GRCh38.p7 | 14:20382203 | CCTCAGCCTCCCAAC[A/C/T]AACCCACCCCAAGCA | 7011 |
rs760819869 | snp | A/G | 1.64893e-05 | 0.0028713 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380959 | GGCCTCCAAGAGCCG[A/G]GAGACCAGACCCAAT | 7011 |
rs760829622 | in-del | -/GG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410800 | TTGTTTCTCCTTTGT[-/GG]GGTTTTTTTTTTTTT | 7011 |
rs760840090 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20382541 | CACAAGACAGCAAAG[A/G]ACGTGGGATAGGGAT | 7011 |
rs760851752 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410896 | GCACAGTCTCAGCTC[A/G]CTGCAACCTCGACTT | 7011 |
rs760861309 | snp | A/G | 1.65029e-05 | 0.00287248 | intron-variant | TEP1 | GRCh38.p7 | 14:20390767 | CAAACTCCTGAAGGA[A/G]AGAGACTTCATGTTA | 7011 |
rs760862962 | snp | A/C/T | 3.29501e-05 | 0.00405884 | intron-variant | TEP1 | GRCh38.p7 | 14:20386217 | GCATGATGATAGGGA[A/C/T]GTGTGGGAGTCACTG | 7011 |
rs760883519 | snp | A/G | 4.94882e-05 | 0.0049741 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368446 | ACATCTTCATTCCCA[A/G]TTCAGAAAGTACACA | 7011 |
rs760888132 | snp | G/T | 1.65187e-05 | 0.00287386 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384111 | GGCAGCATCAGCCGT[G/T]GCACTGTGTCCTGAA | 7011 |
rs760905105 | snp | A/G | 1.64779e-05 | 0.00287031 | intron-variant | TEP1 | GRCh38.p7 | 14:20372874 | TGGTGTACACAACAA[A/G]TTCAATTCAGTGCTT | 7011 |
rs760908880 | snp | A/G | 3.44122e-05 | 0.00414788 | intron-variant | TEP1 | GRCh38.p7 | 14:20380486 | AGAAGCTATAAAAGG[A/G]TGGCAGAATGTCACT | 7011 |
rs760929596 | snp | C/T | 1.65209e-05 | 0.00287405 | intron-variant | TEP1 | GRCh38.p7 | 14:20400963 | GAGAAGGAGGGAATG[C/T]GATGGTCAAGGTCAC | 7011 |
rs760941445 | snp | A/G | 1.65493e-05 | 0.00287652 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404657 | GAAGGCAGCTGGACA[A/G]TGGCACAGAAATATC | 7011 |
rs760943517 | in-del | -/ATGT | 1.74909e-05 | 0.00295722 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383633 | TCTGCTGCAGCTCCC[-/ATGT]ACACCAGGCTTCTGT | 7011 |
rs760958776 | snp | C/T | 1.66073e-05 | 0.00288156 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401606 | CATCCCCAAGTCCCA[C/T]AGGGGTCCTTTCATC | 7011 |
rs760984893 | snp | A/G | 1.71578e-05 | 0.00292893 | intron-variant | TEP1 | GRCh38.p7 | 14:20405621 | AAGAAATGAGAAGAG[A/G]GGTAACAAGGACCAA | 7011 |
rs761032947 | snp | C/T | 1.65304e-05 | 0.00287488 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384687 | GACTCAGAAACAAAG[C/T]CAGATTTCCAGGCAT | 7011 |
rs761047021 | snp | A/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371298 | ACAATATCATAGGAT[A/T]TTCTGTATAGCTGCT | 7011 |
rs761059324 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392737 | TATGGACTAAATAAC[A/G]GATGATTTCACCGAG | 7011 |
rs761061174 | snp | C/T | 4.94287e-05 | 0.00497111 | missense, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401502 | GCAGGCTTGTGGATG[C/T]GCAGTCGCTGAACCA | 7011 |
rs761112387 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408034 | AATCAGCTTGCGTCA[C/T]GTGAGATATCTGTAG | 7011 |
rs761115756 | snp | C/T | 1.66322e-05 | 0.00288371 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383559 | ACCTATCAGCCCCAT[C/T]GATGATCAGGACCTG | 7011 |
rs761116066 | snp | C/G | 1.64988e-05 | 0.00287213 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395547 | GGCTTAGGTGGCAAA[C/G]AAACCTCCGCCTGGG | 7011 |
rs761123055 | in-del | -/TCTTCAAA | 3.29598e-05 | 0.00405941 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369750 | TCAAAGTTCAGCCTC[-/TCTTCAAA]TCTTCAAACTCTCCT | 7011 |
rs761132579 | snp | A/G | 3.29516e-05 | 0.00405891 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384609 | GCTCACCTGCGGCAG[A/G]TGATCCCTTTCTGTC | 7011 |
rs761151526 | snp | A/G/T | 3.34388e-05 | 0.00408883 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395619 | TTATATTCGAAGGAA[A/G/T]GGGCAATGCTGTATG | 7011 |
rs761176683 | snp | A/G | 4.94597e-05 | 0.00497266 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379022 | CTCCAGGAGCCCGTC[A/G]AAGGCAGTAAGAAAG | 7011 |
rs761210220 | snp | C/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377645 | CCGCTCGATATCCAA[C/G]AGCCACCCGATCACC | 7011 |
rs761243496 | snp | A/G | 3.29859e-05 | 0.00406102 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391074 | ATCATCCCAATCAAC[A/G]GCAGTGCATAGTTCA | 7011 |
rs761255001 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371223 | TAGGACTTACCAAGA[A/G]AGAAAGAACTCCAGG | 7011 |
rs761258468 | snp | C/T | 5.22071e-05 | 0.00510889 | utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408453 | ATGGCTGAAACTCAG[C/T]TTGTATATGCCTAGA | 7011 |
rs761271913 | snp | A/G | 3.90457e-05 | 0.0044183 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383911 | TGCAGGGCTGACACA[A/G]GAGATGCCTGCATGG | 7011 |
rs761286817 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405093 | ATTGATTAAACCTGC[C/T]ATTTTCCAAAGCATC | 7011 |
rs761301855 | snp | A/C | 3.31636e-05 | 0.00407194 | intron-variant | TEP1 | GRCh38.p7 | 14:20386061 | CAGCCCTCCTCCAAA[A/C]CTGTCTGCCTTACCC | 7011 |
rs761323334 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382655 | AGAGCCTCAGGTGAT[C/T]GGTGACCAAGCGCAG | 7011 |
rs761347422 | snp | G/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373311 | CGTACAGAACCATCC[G/T]CAGAGGCGGTCAGCA | 7011 |
rs761373776 | snp | A/G | 5.87745e-05 | 0.00542068 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383812 | CAGAGGCGTCTGAGC[A/G]GAGTGAGGGCAAGAC | 7011 |
rs761374373 | snp | A/G | 3.47156e-05 | 0.00416612 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368878 | CAGGTAGCACATGGA[A/G]GGCTGTGACAGAGCC | 7011 |
rs761412035 | snp | A/C | 1.76808e-05 | 0.00297323 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396675 | GGAACTGATTCCAAC[A/C]CGCAGCAGGTTGCAC | 7011 |
rs761419752 | in-del | -/C | 1.64751e-05 | 0.00287007 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403372 | CCCCAGAAGAAGGGA[-/C]TCACCTTTCTCTGCT | 7011 |
rs761427887 | snp | C/T | 4.95242e-05 | 0.0049759 | intron-variant | TEP1 | GRCh38.p7 | 14:20378333 | TCTGCCACCCTCCAC[C/T]CCTGTCCTCCTGTGC | 7011 |
rs761427965 | snp | C/G | 1.65765e-05 | 0.00287888 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376128 | GCCCCCGGTGGCCAG[C/G]CTGCCTCCATCAGTG | 7011 |
rs761449081 | snp | C/T | | | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406284 | ATGAGATTCAGAGTC[C/T]CCAGAGGTGAGCTTC | 7011 |
rs761451870 | snp | C/T | 5.03436e-05 | 0.0050169 | intron-variant | TEP1 | GRCh38.p7 | 14:20406449 | GGTATCCACAGCCCC[C/T]CAAAGCCAGATGGAT | 7011 |
rs761457056 | snp | C/G | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377607 | TTCAGTACCTGAAGA[C/G]ATTTTGTAGATCCTA | 7011 |
rs761488622 | snp | A/T | 3.43891e-05 | 0.00414649 | intron-variant | TEP1 | GRCh38.p7 | 14:20395424 | CCCGATTGCCCACCC[A/T]TGGCTCCCAGACAGT | 7011 |
rs761518113 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388198 | CTTAAGAAGAGGACC[-/A]ATAAGCAGTTTATGC | 7011 |
rs761522474 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410008 | CCTGGGCGACAGAGC[A/G]AGACTCTGTCTCAAA | 7011 |
rs761525669 | in-del | -/GGGCTTACTAGGGTCTGGGGTCAA | 3.40408e-05 | 0.00412544 | intron-variant | TEP1 | GRCh38.p7 | 14:20380203 | AGCTTGCTCTCTGGT[-/GGGCTTACTAGGGTCTGGGGTCAA]GGTCTTACCTTTGCT | 7011 |
rs761562116 | snp | C/G | 1.65507e-05 | 0.00287664 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381922 | CTGTACCTGCGCAGA[C/G]TCTGGACGAGGCAGG | 7011 |
rs761565557 | snp | A/G | 1.65312e-05 | 0.00287495 | intron-variant | TEP1 | GRCh38.p7 | 14:20389230 | TTCAGTATCCATTCT[A/G]TACTCACTTCAGTAT | 7011 |
rs761577651 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411497 | CTGATTTAGGTGGCC[C/T]TCTCCTTGTTTTCAC | 7011 |
rs761580777 | snp | C/T | 1.65228e-05 | 0.00287422 | intron-variant | TEP1 | GRCh38.p7 | 14:20377511 | GAGAATGAGAGAGAA[C/T]AAGGGAGTAAGACAC | 7011 |
rs761596899 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20389468 | AGTTAGGCTAAAGTA[C/T]CCACCTGAAGTGCAA | 7011 |
rs761613587 | snp | C/T | 3.35284e-05 | 0.00409427 | intron-variant | TEP1 | GRCh38.p7 | 14:20380066 | GAGCTAGAGAAAGAG[C/T]AGGAAGAAAGGGAGG | 7011 |
rs761613906 | snp | A/C | 0.00237243 | 0.0343597 | intron-variant | TEP1 | GRCh38.p7 | 14:20391146 | CCTGCTTTGGAATTC[A/C]CCCTTGCCCAGCCAG | 7011 |
rs761622385 | snp | C/T | 1.65302e-05 | 0.00287486 | intron-variant | TEP1 | GRCh38.p7 | 14:20389339 | CCATCACAAACAATA[C/T]CTGGAACACAGTCAC | 7011 |
rs761675754 | snp | A/C | 1.65111e-05 | 0.0028732 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389687 | GTAAAGCTGTTTGGC[A/C]ACATTTATCATTCCA | 7011 |
rs761740469 | snp | A/G | 1.82141e-05 | 0.00301773 | intron-variant | TEP1 | GRCh38.p7 | 14:20383356 | CCAGGTGTACACACT[A/G]TGATATTTGGGCAAA | 7011 |
rs761753885 | snp | C/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402028 | TGCCTATAAACCTAA[C/T]ACTTTGGGAGGCCAA | 7011 |
rs761769323 | snp | A/G | 4.94629e-05 | 0.00497283 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373684 | TTTTGTTACCTGCAC[A/G]GGGCTCCATGGCAGC | 7011 |
rs761780865 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403477 | AGAAGCAATTTCAAA[A/G]AAAGGGAACTGGCTG | 7011 |
rs761817163 | snp | A/G | 1.64961e-05 | 0.00287189 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380260 | TTTTCATGGTCCGGG[A/G]TTTATTAAGCCATCG | 7011 |
rs761822184 | snp | A/G | 1.65059e-05 | 0.00287275 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373751 | GCTGGTCAGCTCCAC[A/G]CCTTGATGGTCCCAC | 7011 |
rs761830674 | snp | A/G | 1.65323e-05 | 0.00287505 | intron-variant | TEP1 | GRCh38.p7 | 14:20403703 | AGGGGCGTGGGTCGA[A/G]GGCTGGGGCAGTGAC | 7011 |
rs761839755 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20390561 | GGTTGTAGCCAGTAG[A/T]GCTGATCTGACTATT | 7011 |
rs761864592 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373072 | CCAGCTTGATTTCCA[A/G]ATACTGCCATGGAAC | 7011 |
rs761873362 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376468 | AGGACGGGAACGTGC[A/G]GCACTCCCAGCTCCA | 7011 |
rs761875973 | snp | A/G | 1.65321e-05 | 0.00287502 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382278 | GGACATCAGGCCCGT[A/G]CTCCTTCTCCAGTGT | 7011 |
rs761877966 | snp | A/C | 1.79406e-05 | 0.00299499 | intron-variant | TEP1 | GRCh38.p7 | 14:20380521 | AGCCAGCTGGACCCC[A/C]TTAGCCCCAGCACCA | 7011 |
rs761886754 | snp | A/C | 1.68766e-05 | 0.00290483 | intron-variant | TEP1 | GRCh38.p7 | 14:20375881 | ACTCTGGATAGGCCC[A/C]AAGGAGAGGGAGCAA | 7011 |
rs761931409 | snp | C/G | 4.94531e-05 | 0.00497234 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380985 | CCAATTCCAAGTGTG[C/G]AGCCACCACATGGAG | 7011 |
rs761935601 | snp | A/C | 1.64746e-05 | 0.00287002 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390985 | TCAGGATGCCTTCTT[A/C]TGCCTTAAGCACTGC | 7011 |
rs761938046 | in-del | -/TC | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406801 | TCTGAACCTCAGCTT[-/TC]TCTCATTCACTACCA | 7011 |
rs761940855 | snp | C/T | 1.67624e-05 | 0.00289498 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404730 | CCAAGATGTTATTGG[C/T]CACATTCCGGACGTT | 7011 |
rs761958847 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378827 | CAGCCAGTGATTTGG[C/T]ACTGGTGAGCCTTAG | 7011 |
rs761965366 | snp | C/T | | | | | GRCh38.p7 | 14:20415977 | ATCGAAAACCTTCAT[C/T]AGTGGTCTGTTTAGA | 7011 |
rs761966382 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401060 | CTCTGGCCTAGACAG[C/T]TTCATCCTCTTCCCA | 7011 |
rs761982249 | snp | C/T | 1.64982e-05 | 0.00287208 | intron-variant | TEP1 | GRCh38.p7 | 14:20369641 | CACCCTGGGCCATCT[C/T]CCGGCTCCTCAGGTC | 7011 |
rs762003846 | snp | A/G | 3.5251e-05 | 0.00419812 | intron-variant | TEP1 | GRCh38.p7 | 14:20401162 | GATAGGTAAGAAAGA[A/G]GTCTATCATTTCAGA | 7011 |
rs762016417 | snp | A/G | 1.65433e-05 | 0.002876 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384198 | ACCAAGTCATCGTCT[A/G]GGATGGACACTGGCT | 7011 |
rs762035454 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369524 | TCCTTCTGGGCTGCA[C/T]TTGGCCAGGTTCCAT | 7011 |
rs762056316 | snp | C/G | 1.65373e-05 | 0.00287548 | intron-variant | TEP1 | GRCh38.p7 | 14:20378739 | ACTCTGACCACTGCA[C/G]ACCCCAAGTCTTACC | 7011 |
rs762071558 | snp | A/G | 3.29598e-05 | 0.00405941 | intron-variant | TEP1 | GRCh38.p7 | 14:20384349 | AACCCAGACCACCCC[A/G]TGTCCCTCTCCATGC | 7011 |
rs762113016 | snp | C/T | 3.29685e-05 | 0.00405995 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377418 | CTTCTGCACCACTCA[C/T]CAATACCTTGGGGCT | 7011 |
rs762115583 | snp | C/T | 6.71783e-05 | 0.00579523 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395626 | CGAAGGAAAGGGCAA[C/T]GCTGTATGATGACAG | 7011 |
rs762160300 | snp | A/G | 1.65422e-05 | 0.0028759 | intron-variant | TEP1 | GRCh38.p7 | 14:20391772 | ATTTCCACTGTCTAC[A/G]TGCAAGAAAGACACA | 7011 |
rs762167017 | snp | A/G | 1.67332e-05 | 0.00289246 | intron-variant | TEP1 | GRCh38.p7 | 14:20395817 | CTTCATTTATTGTCA[A/G]ATGTGGGAGGCAAAG | 7011 |
rs762169194 | snp | C/G | 2.03266e-05 | 0.00318793 | intron-variant | TEP1 | GRCh38.p7 | 14:20383730 | AAGGCTGGGCTCATT[C/G]GGGGATACCCACCGG | 7011 |
rs762179399 | snp | C/T | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368525 | AGCCAAGGTTCCAGG[C/T]AGCTCACTGACCCTT | 7011 |
rs762190945 | in-del | -/CCAGCCTGGGCAACAAGAACGAAAC | 1.65146e-05 | 0.0028735 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373770 | GATGGTCCCACACTT[-/CCAGCCTGGGCAACAAGAACGAAAC]TCAAGGTCCCATCCC | 7011 |
rs762213321 | snp | A/C | 1.67049e-05 | 0.00289002 | intron-variant | TEP1 | GRCh38.p7 | 14:20384718 | CTGGCACAGAGCTGA[A/C]CACCAAAGACCCCAA | 7011 |
rs762218522 | in-del | -/A | 1.64746e-05 | 0.00287002 | intron-variant | TEP1 | GRCh38.p7 | 14:20371205 | CTTTAGCACACACTC[-/A]AATAGGACTTACCAA | 7011 |
rs762224177 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20371326 | GCTCCTGGTTTGTGA[C/G]AAAGGAATAGGTTGA | 7011 |
rs762230665 | snp | A/T | 0.000115484 | 0.00759794 | intron-variant | TEP1 | GRCh38.p7 | 14:20373223 | GGCCACCCTTGACCT[A/T]TTTTTGTGCCAGTAA | 7011 |
rs762248758 | snp | A/G | 1.65187e-05 | 0.00287386 | intron-variant | TEP1 | GRCh38.p7 | 14:20382215 | AACCAACCCACCCCA[A/G]GCACTGACCACTCCG | 7011 |
rs762268342 | snp | C/G | 9.33768e-05 | 0.00683225 | intron-variant | TEP1 | GRCh38.p7 | 14:20383667 | TGGAGAGGAAGTCAG[C/G]GTCAGTGGGAGAGAA | 7011 |
rs762329428 | snp | A/G | 0.000215794 | 0.0103851 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377726 | GGTGCCCACGGGGCC[A/G]ACCCAGAGACCCTGA | 7011 |
rs762331108 | snp | A/T | 3.4181e-05 | 0.00413393 | intron-variant | TEP1 | GRCh38.p7 | 14:20379921 | TCTGCCCCTCCTTGA[A/T]TGTCATACCTGCCAA | 7011 |
rs762367874 | snp | A/G | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415011 | CATACCACCCCGAAC[A/G]CGCCCGATCTCCTCT | 7011 |
rs762368464 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20371704 | GGCTCCTCAATCCCA[C/T]ATGAATTCCTCAGGA | 7011 |
rs762380200 | snp | C/T | 1.67598e-05 | 0.00289476 | intron-variant | TEP1 | GRCh38.p7 | 14:20377986 | TTTGCCTTTGCTACT[C/T]CTCCTCACAACCCAC | 7011 |
rs762408623 | snp | C/T | 1.65015e-05 | 0.00287237 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382710 | CTTCACCAGCAGCAG[C/T]CGCATCTGGCAAGAC | 7011 |
rs762436649 | snp | C/T | 1.65883e-05 | 0.00287991 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384093 | AGGCTCAGCCTTCCG[C/T]GGGGCAGCATCAGCC | 7011 |
rs762456085 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408251 | CACATATCCATGTGG[C/T]TTTTCCATGGTCTTC | 7011 |
rs762456144 | snp | C/T | 8.26617e-05 | 0.00642838 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404672 | ATGGCACAGAAATAT[C/T]GTCGCAGGTGGGGGC | 7011 |
rs762480078 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371237 | AAAGAAAGAACTCCA[A/G]GATCCTTGGGCTGCA | 7011 |
rs762490163 | snp | C/G | 2.12538e-05 | 0.00325982 | intron-variant | TEP1 | GRCh38.p7 | 14:20377243 | AAGAAAAGAAAAGAA[C/G]AGTAATTTGTTAACC | 7011 |
rs762496372 | snp | C/T | 1.72531e-05 | 0.00293705 | intron-variant | TEP1 | GRCh38.p7 | 14:20405624 | AAATGAGAAGAGAGG[C/T]AACAAGGACCAACTT | 7011 |
rs762496456 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376335 | CCTGGGAGGCCAAAG[A/T]CAGGAGCGGCCATGG | 7011 |
rs762562093 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391651 | TTAGCATCTGTCAGA[C/T]AGACCAAGACAGTGC | 7011 |
rs762588377 | snp | C/T | 3.30502e-05 | 0.00406497 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389246 | TACTCACTTCAGTAT[C/T]GCATCAGTACAGCCT | 7011 |
rs762591405 | snp | C/T | 3.37456e-05 | 0.00410751 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376262 | GCTGCACTGTGAAAT[C/T]CTCTGCATTGGAAAA | 7011 |
rs762612248 | snp | C/T | 3.29457e-05 | 0.00405854 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403766 | CTCTTGGCCCGGTGC[C/T]TCCGAGGGTTGTACT | 7011 |
rs762615438 | snp | A/G | 1.64808e-05 | 0.00287057 | intron-variant | TEP1 | GRCh38.p7 | 14:20373426 | AAGGGATGGAGATGG[A/G]CTCATGAGAGTGGGC | 7011 |
rs762620459 | snp | G/T | 1.65291e-05 | 0.00287476 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389706 | TTTATCATTCCATCA[G/T]CCATGCTTTGGCCAA | 7011 |
rs762633808 | snp | C/T | 1.66535e-05 | 0.00288556 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401622 | AGGGGTCCTTTCATC[C/T]ATGACCATGGGAACT | 7011 |
rs762667357 | snp | C/T | 0.000109258 | 0.00739033 | intron-variant | TEP1 | GRCh38.p7 | 14:20396610 | CATGGCTACCAGCCC[C/T]TCACACATACCGCAT | 7011 |
rs762673311 | snp | C/T | 1.66051e-05 | 0.00288137 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381675 | CGCTCCAGAGGGCCC[C/T]CCCCTAGCAAACTGT | 7011 |
rs762700538 | snp | C/G | 3.33589e-05 | 0.00408391 | intron-variant | TEP1 | GRCh38.p7 | 14:20379117 | CCTCCTGCGACAGTG[C/G]GTGAGGGAGCGCAGC | 7011 |
rs762705933 | snp | C/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406283 | GATGAGATTCAGAGT[C/G]TCCAGAGGTGAGCTT | 7011 |
rs762708627 | snp | A/G | 0.000148303 | 0.00860985 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380275 | GTTTATTAAGCCATC[A/G]TAGTGTGTGTTGGAG | 7011 |
rs762712265 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410142 | ACTAAGTGTTCAATA[C/T]AGAAGCTATTATTAT | 7011 |
rs762759586 | snp | A/G | 1.65075e-05 | 0.00287289 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378222 | ACGGATAGAGGCTCC[A/G]GGTGCCCCCAGGTCC | 7011 |
rs762776607 | snp | C/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401717 | GATTTGGCCAAGGAG[C/T]AGGAATAGAGGGTAC | 7011 |
rs762785016 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367811 | AGACAGGGTTTCACT[A/G]TGTTAGCCAGGATGG | 7011 |
rs762798971 | in-del | -/A | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20383680 | GGGTCAGTGGGAGAG[-/A]AAAAAAAAAGCAGGG | 7011 |
rs762811325 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372769 | CCCTTCCGCAGTTTC[A/G]CTTGCCACTCGCTGA | 7011 |
rs762818870 | snp | A/G | 1.64762e-05 | 0.00287016 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403840 | GGCAGTACGGAGACA[A/G]GCGGGCAGGGGCACC | 7011 |
rs762838981 | snp | A/C | 1.64966e-05 | 0.00287194 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382005 | TTCCCAGCTCTTAGT[A/C]CCCTTCGGTAGTGTC | 7011 |
rs762859046 | in-del | -/CGGTGAGGGGCCGCT | 1.66957e-05 | 0.00288922 | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386510 | CCGTGAAGGCTGATA[-/CGGTGAGGGGCCGCT]CGGGCCTGCAGTGCT | 7011 |
rs762893062 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20384035 | GCCCCTGAGACTCTG[C/T]ACCAGGAAGGCTGTC | 7011 |
rs762910591 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | TEP1 | GRCh38.p7 | 14:20372861 | GTGGCCTGGAGCCTG[A/G]TGTACACAACAAGTT | 7011 |
rs762913672 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400049 | TAATCCCAGCTACTC[A/G]GGAGACTGAGGCAGG | 7011 |
rs762919387 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | TEP1 | GRCh38.p7 | 14:20384376 | ATGCCTCTGGTCACC[A/G]GTGCTTCTGCTGACC | 7011 |
rs762994301 | snp | C/T | 0.000100013 | 0.00707083 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386574 | GCAGGTCCCGCTCCC[C/T]ATGCATGTCTCGGAA | 7011 |
rs763011100 | snp | A/G | 1.78576e-05 | 0.00298806 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396677 | AACTGATTCCAACCC[A/G]CAGCAGGTTGCACAG | 7011 |
rs763053666 | in-del | -/AGA | 1.64808e-05 | 0.00287057 | intron-variant | TEP1 | GRCh38.p7 | 14:20371367 | TAAAGAGAGGTAAAG[-/AGA]AGAACACCTCTCTTT | 7011 |
rs763074831 | snp | A/G | 7.1253e-05 | 0.00596837 | intron-variant | TEP1 | GRCh38.p7 | 14:20401167 | GTAAGAAAGAGGTCT[A/G]TCATTTCAGAGTCAG | 7011 |
rs763088602 | snp | A/G | 3.40663e-05 | 0.00412698 | intron-variant | TEP1 | GRCh38.p7 | 14:20395438 | CTTGGCTCCCAGACA[A/G]TGCATACATACCTGG | 7011 |
rs763120742 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384492 | CAGCTGCCACACCCC[C/T]CCACTCACAGGGGTA | 7011 |
rs763127688 | snp | A/G | 8.24559e-05 | 0.00642037 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378982 | GGAGGACCCCTTACC[A/G]ACAACCATGCTGCAG | 7011 |
rs763140440 | snp | A/T | 1.65012e-05 | 0.00287234 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20401455 | AGGGTGCAGCTTCTC[A/T]CCTGTAACCCAGCAG | 7011 |
rs763165977 | snp | A/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403319 | GAATTTTGTTCGTAA[A/T]TATTAGTCCAGAAGA | 7011 |
rs763174088 | snp | G/T | 1.80211e-05 | 0.0030017 | intron-variant | TEP1 | GRCh38.p7 | 14:20383374 | ATATTTGGGCAAAGG[G/T]GCAGGAAGGTAGAAA | 7011 |
rs763182650 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377631 | GATCCTAATGCCATC[C/T]GCTCGATATCCAACA | 7011 |
rs763185234 | snp | A/C | 0.000164818 | 0.00907644 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20373268 | CTCCAAGCCTCACTC[A/C]CCTGCTTCCTTAGGA | 7011 |
rs763204917 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403161 | CATAACTTCATCTCA[-/AA]AAAAAAAAAAAAAAA | 7011 |
rs763209347 | snp | A/G | 1.65323e-05 | 0.00287505 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407939 | AGGGCAGGTTGAAAG[A/G]TCTAGTCCCTTAGAG | 7011 |
rs763259332 | snp | A/G/T | 0.000231713 | 0.0107613 | intron-variant | TEP1 | GRCh38.p7 | 14:20390801 | GGTTGCACAGTAAGC[A/G/T]ACAAACACTGCAGTC | 7011 |
rs763305917 | snp | C/T | 0.000638801 | 0.0178604 | intron-variant | TEP1 | GRCh38.p7 | 14:20368763 | AGGTGTGCAGGCGCA[C/T]GCACACACACACACA | 7011 |
rs763306126 | snp | A/G | 1.66815e-05 | 0.00288799 | intron-variant | TEP1 | GRCh38.p7 | 14:20389585 | CTGATTTCTGACACT[A/G]GGCAGGAAGTATAAG | 7011 |
rs763326953 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397548 | CACCATTTATAATGA[C/T]GAATGTATGTAAATC | 7011 |
rs763332766 | snp | A/G | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395919 | CGTTAAGAAATCTGA[A/G]TGGAAACTGCCGACT | 7011 |
rs763378251 | snp | A/G | 1.76852e-05 | 0.0029736 | intron-variant | TEP1 | GRCh38.p7 | 14:20381095 | AAGGGGCTGGTGAGA[A/G]GGGACAGTTTAGTCT | 7011 |
rs763390969 | snp | C/G | 1.66203e-05 | 0.00288268 | intron-variant | TEP1 | GRCh38.p7 | 14:20406412 | GACCCTGGGGTAGTA[C/G]TGGCAGTTATGAATC | 7011 |
rs763412665 | snp | C/T | 1.65831e-05 | 0.00287945 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382295 | TCCTTCTCCAGTGTG[C/T]TCAGGATGTGCTGCA | 7011 |
rs763433318 | snp | A/G | 3.33884e-05 | 0.00408572 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386506 | GATTCCGTGAAGGCT[A/G]ATACGGTGAGGGGCC | 7011 |
rs763441012 | snp | C/G | 1.65018e-05 | 0.00287239 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378090 | CGCAGCAGCAACAAA[C/G]CCATGGTGGGCAGGG | 7011 |
rs763448875 | snp | C/T | 3.94197e-05 | 0.00443941 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383803 | AGATAGGTACAGAGG[C/T]GTCTGAGCAGAGTGA | 7011 |
rs763466192 | snp | A/C/T | 5.92872e-05 | 0.00544432 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383764 | GTGCTGGGGAGGGCA[A/C/T]CTGGCTCTTTTAGTT | 7011 |
rs763470035 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381009 | CATGGAGGTTGGTAA[A/G]GAACTTCGAAAGAAG | 7011 |
rs763477449 | snp | C/T | 1.70026e-05 | 0.00291565 | intron-variant | TEP1 | GRCh38.p7 | 14:20375743 | CTGTGCCACCCCTGG[C/T]CCTTTACTCACCAGT | 7011 |
rs763513216 | snp | A/T | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371578 | ACCATCAGGAGCCCA[A/T]TCCAGACTTGTCAGC | 7011 |
rs763568850 | snp | A/G | 1.66073e-05 | 0.00288156 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378039 | CTTGCCATCCTCTCC[A/G]GCCGTCAGTAACTGG | 7011 |
rs763572873 | snp | A/G | 5.02441e-05 | 0.00501194 | intron-variant | TEP1 | GRCh38.p7 | 14:20380063 | CTGGAGCTAGAGAAA[A/G]AGTAGGAAGAAAGGG | 7011 |
rs763580637 | in-del | -/G | 0.000115818 | 0.00760892 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401586 | GCCTTCTCAAACTGT[-/G]GAAACATCCCCAAGT | 7011 |
rs763593276 | snp | C/T | 1.83458e-05 | 0.00302862 | intron-variant | TEP1 | GRCh38.p7 | 14:20404811 | AGAATCTCAGTCACT[C/T]CTCCCGTAGCTTTCT | 7011 |
rs763612696 | snp | A/G | 1.65198e-05 | 0.00287395 | intron-variant | TEP1 | GRCh38.p7 | 14:20385119 | CTGGGCCTGCGGGGA[A/G]GACAGAGACAGTGAG | 7011 |
rs763621785 | snp | A/C | 3.29962e-05 | 0.00406165 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378114 | GGCAGGGAAGGCAGC[A/C]AGCCGTGCCCCTTCT | 7011 |
rs763643878 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408288 | GGAAGCGTGGCTAGG[C/T]ACTGGTTCTTCAAGG | 7011 |
rs763667481 | snp | C/T | 9.281e-05 | 0.00681149 | intron-variant | TEP1 | GRCh38.p7 | 14:20404818 | CAGTCACTCCTCCCG[C/T]AGCTTTCTGCCCTGA | 7011 |
rs763668337 | snp | C/T | 0.000137372 | 0.00828657 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383806 | TAGGTACAGAGGCGT[C/T]TGAGCAGAGTGAGGG | 7011 |
rs763685829 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391068 | GTGATCATCATCCCA[A/G]TCAACAGCAGTGCAT | 7011 |
rs763689393 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20389309 | TGACCTGGCAAAGGA[A/G]GAAGCAGTCATTAAC | 7011 |
rs763697276 | snp | C/T | 1.68306e-05 | 0.00290087 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408426 | GCAGACACATGCCCA[C/T]GGAGTTTTTCCATGG | 7011 |
rs763703443 | in-del | -/CT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372616 | GAAAATAATGTCCCA[-/CT]CAGTAACTAACATCC | 7011 |
rs763705729 | snp | A/G | 1.67036e-05 | 0.0028899 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382310 | CTCAGGATGTGCTGC[A/G]GCAGCAGGGGGACAG | 7011 |
rs763707095 | snp | C/T | 1.78745e-05 | 0.00298947 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20383173 | CGGCCTAGAACCCAA[C/T]CTGGTTGTTAAATGG | 7011 |
rs763707739 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376431 | GAGGCCCTGGGCAAG[G/T]GTCATCAGCGAGTGT | 7011 |
rs763764878 | snp | A/G | 1.67262e-05 | 0.00289185 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386516 | AGGCTGATACGGTGA[A/G]GGGCCGCTCGGGCCT | 7011 |
rs763772775 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406133 | TAGGTTGTATCCCTA[C/T]CTTCCCCTTCCAACT | 7011 |
rs763778595 | snp | C/G/T | 0.000115318 | 0.00759261 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391025 | AGTGTCACCTCCACA[C/G/T]AGCACGACGTCCACC | 7011 |
rs763805137 | in-del | -/A | 1.64882e-05 | 0.00287121 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390753 | TCCATCATTTTCATC[-/A]AACTCCTGAAGGAAA | 7011 |
rs763809958 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20388004 | GGTGGAATCTTGAAT[A/G]TTTTGTCCATTTGGC | 7011 |
rs763818029 | snp | C/T | 1.65056e-05 | 0.00287272 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391756 | AGCATCTCACCATCA[C/T]ATTTCCACTGTCTAC | 7011 |
rs763846172 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367825 | TATGTTAGCCAGGAT[C/G]GTCTTGATCTCCTGA | 7011 |
rs763900428 | snp | A/C | 1.64893e-05 | 0.0028713 | intron-variant | TEP1 | GRCh38.p7 | 14:20382401 | GTGCAGTGGGAGGAG[A/C]AGCAGCTTGGCTTGT | 7011 |
rs763910539 | snp | A/G | 0.000109196 | 0.00738824 | intron-variant | TEP1 | GRCh38.p7 | 14:20383159 | ACACCCACCGGCCCC[A/G]GCCTAGAACCCAACC | 7011 |
rs763924150 | in-del | -/G | 5.09649e-05 | 0.00504776 | intron-variant | TEP1 | GRCh38.p7 | 14:20375912 | TCAGGACCAAAGGAA[-/G]GATGGGAACCCCGGA | 7011 |
rs763944131 | snp | C/G | 1.65985e-05 | 0.00288079 | intron-variant | TEP1 | GRCh38.p7 | 14:20395850 | GAGTTGGAAGAAAGG[C/G]GAGAATACCTTGATT | 7011 |
rs763961398 | snp | A/G | 1.70206e-05 | 0.00291719 | intron-variant | TEP1 | GRCh38.p7 | 14:20381702 | CTGTCCTCGTGTGAG[A/G]AAGGGAGAGAGAAGA | 7011 |
rs763965798 | snp | A/G | 3.39945e-05 | 0.00412263 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377284 | TCTAGTAGTACCTGA[A/G]GCAGAAGCCAAGAGC | 7011 |
rs763980620 | snp | G/T | 4.95119e-05 | 0.00497529 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385014 | ATCCCGGAAGTAGAT[G/T]AGAGCTTGGGCAGAG | 7011 |
rs764003289 | snp | A/G | 6.6302e-05 | 0.00575731 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381917 | GGCACCTGTACCTGC[A/G]CAGACTCTGGACGAG | 7011 |
rs764006091 | snp | A/G | 1.6549e-05 | 0.0028765 | intron-variant | TEP1 | GRCh38.p7 | 14:20389201 | TAAAAACTTTCCAAC[A/G]AAGTATCCAACCCTT | 7011 |
rs764015021 | snp | G/T | 1.64855e-05 | 0.00287097 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377395 | TGCCCAGCCCTGCAA[G/T]GACCCATCTTCTGCA | 7011 |
rs764025044 | snp | A/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406318 | GCCAGATCCTCCACC[A/T]CCTCCTCCTCTCCCA | 7011 |
rs764085340 | snp | C/G | 3.30978e-05 | 0.0040679 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379959 | GGTCCAACAGGTAAA[C/G]TGTCCCATTGGCAGT | 7011 |
rs764103326 | snp | C/G | 1.72335e-05 | 0.00293538 | intron-variant | TEP1 | GRCh38.p7 | 14:20380489 | AGCTATAAAAGGGTG[C/G]CAGAATGTCACTGGG | 7011 |
rs764202002 | snp | A/T | 1.65083e-05 | 0.00287296 | intron-variant | TEP1 | GRCh38.p7 | 14:20400969 | GAGGGAATGTGATGG[A/T]CAAGGTCACTCTACC | 7011 |
rs764203379 | snp | C/G | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380415 | TGCTGCCTCAGGAAG[C/G]TGCGAAACACTGCAA | 7011 |
rs764224282 | snp | A/G | 1.82693e-05 | 0.00302231 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374522 | CCCCACAGAGCCATC[A/G]CTGGAGCAGGATATC | 7011 |
rs764290873 | in-del | -/AAG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20396137 | GAGAAAAGGTAACAA[-/AAG]AAGAGAAAGTAACAG | 7011 |
rs764317784 | in-del | -/CA/CACA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368758 | GGATAGGTGTGCAGG[-/CA/CACA]CGCACGCACACACAC | 7011 |
rs764320766 | snp | G/T | 0.000115383 | 0.00759462 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384610 | CTCACCTGCGGCAGG[G/T]GATCCCTTTCTGTCT | 7011 |
rs764345884 | snp | C/T | 3.29554e-05 | 0.00405914 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373056 | CCACAAGATTAGTTC[C/T]CCAGCTTGATTTCCA | 7011 |
rs764373744 | snp | A/G | 5.08169e-05 | 0.00504042 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383239 | CCTCTCTCACCAGCC[A/G]GGCCCGAGCAGAGGC | 7011 |
rs764392080 | snp | C/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377653 | TATCCAACAGCCACC[C/G]GATCACCATCTGGGC | 7011 |
rs764407558 | snp | A/T | 0.000275715 | 0.011738 | intron-variant | TEP1 | GRCh38.p7 | 14:20386443 | TTCTCTGCAGCCCCC[A/T]CACCTGTTCCTACGG | 7011 |
rs764411388 | snp | A/G | 1.65111e-05 | 0.0028732 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384119 | CAGCCGTTGCACTGT[A/G]TCCTGAAGAAGGCGT | 7011 |
rs764423063 | snp | A/T | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395550 | TTAGGTGGCAAAGAA[A/T]CCTCCGCCTGGGACG | 7011 |
rs764445458 | snp | C/G | 4.07141e-05 | 0.0045117 | intron-variant | TEP1 | GRCh38.p7 | 14:20374402 | CCTTCCAGAGACCCC[C/G]CAGTGGGATCTCCAT | 7011 |
rs764445669 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373402 | TGTGGGTTTGGCACA[C/T]CTAGGAGGAAGGGAT | 7011 |
rs764461689 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20370281 | ACCCATGCAGTCACC[C/T]GACAGATCAAGATGT | 7011 |
rs764520385 | snp | A/G | 1.658e-05 | 0.00287919 | intron-variant | TEP1 | GRCh38.p7 | 14:20369784 | TCCTTTTGCCTCTGT[A/G]AAAGAATAGGTAATT | 7011 |
rs764524084 | snp | C/G | 1.64887e-05 | 0.00287125 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379037 | GAAGGCAGTAAGAAA[C/G]AGTGTATCATCGGAG | 7011 |
rs764549133 | in-del | -/AGCTGGCTATACCC | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372174 | ACCAGGAATCCAAGG[-/AGCTGGCTATACCC]AGAATATACTACATA | 7011 |
rs764577100 | snp | A/G | 6.66112e-05 | 0.00577071 | intron-variant | TEP1 | GRCh38.p7 | 14:20379110 | GACTTCTCCTCCTGC[A/G]ACAGTGGGTGAGGGA | 7011 |
rs764641928 | snp | A/C/G | 6.70302e-05 | 0.00578889 | intron-variant | TEP1 | GRCh38.p7 | 14:20382092 | CTCTCTGAGGCCCTC[A/C/G]TCTAACCATACGGTG | 7011 |
rs764644339 | snp | C/G | 1.8272e-05 | 0.00302253 | intron-variant | TEP1 | GRCh38.p7 | 14:20383662 | GTACATGGAGAGGAA[C/G]TCAGGGTCAGTGGGA | 7011 |
rs764658022 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374009 | CAAGAGGCTGTGTTT[A/T]CATGCTCTCCTCTCT | 7011 |
rs764658921 | snp | G/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408041 | TTGCGTCATGTGAGA[G/T]ATCTGTAGACTCTGG | 7011 |
rs764693330 | snp | C/T | 4.94336e-05 | 0.00497135 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390708 | GCCAGCCAGAGACAG[C/T]AGGTATTTCCCAAAA | 7011 |
rs764708941 | snp | A/C | 1.65061e-05 | 0.00287277 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378220 | GTACGGATAGAGGCT[A/C]CGGGTGCCCCCAGGT | 7011 |
rs764725731 | snp | C/G | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413573 | GGAAGGGCAGCGAGC[C/G]GAGGGCCGGGCAAGA | 7011 |
rs764728408 | in-del | -/TT | 0.0424077 | 0.139303 | intron-variant | TEP1 | GRCh38.p7 | 14:20368794 | CACACACACACACAC[-/TT]ACCAGCTGCATACTG | 7011 |
rs764760279 | snp | C/G | 1.6552e-05 | 0.00287676 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376139 | CCAGGCTGCCTCCAT[C/G]AGTGCTGAAACTACA | 7011 |
rs764766485 | snp | A/T | 3.91911e-05 | 0.00442651 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383915 | GGGCTGACACAAGAG[A/T]TGCCTGCATGGGACA | 7011 |
rs764770265 | snp | C/G | 5.0166e-05 | 0.00500804 | intron-variant | TEP1 | GRCh38.p7 | 14:20405406 | ATAACCACACTCCCA[C/G]TCTACCAGCTTCACA | 7011 |
rs764775354 | snp | C/T | 3.29864e-05 | 0.00406105 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391076 | CATCCCAATCAACAG[C/T]AGTGCATAGTTCAGC | 7011 |
rs764781369 | snp | A/G | 1.76817e-05 | 0.00297331 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368883 | AGCACATGGAGGGCT[A/G]TGACAGAGCCCGAGT | 7011 |
rs764813678 | snp | A/G | 1.6684e-05 | 0.00288821 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376246 | AGCTGCCTTGGCCAC[A/G]GCTGCACTGTGAAAT | 7011 |
rs764846215 | snp | C/T | | | | | GRCh38.p7 | 14:20416287 | TCCATCATATTCCCA[C/T]AAATATCAGACCTGA | 7011 |
rs764852991 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381344 | TCTCCCAGAGCCTCA[A/G]GAGGGCAACTTCGGA | 7011 |
rs764872954 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401508 | TTGTGGATGTGCAGT[C/T]GCTGAACCAGCTTCT | 7011 |
rs764929393 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373686 | TTGTTACCTGCACGG[A/G]GCTCCATGGCAGCTG | 7011 |
rs764956827 | snp | G/T | 1.6741e-05 | 0.00289314 | intron-variant | TEP1 | GRCh38.p7 | 14:20389561 | GGCGTAGAGAGGAAA[G/T]GTAGACCACTGATTT | 7011 |
rs764958691 | snp | A/C | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385039 | GCAGAGGGCTGCAGA[A/C]GTTGGTTCCGGTTCA | 7011 |
rs764974451 | snp | C/G | 1.72397e-05 | 0.00293591 | intron-variant | TEP1 | GRCh38.p7 | 14:20391549 | TACTGCTCAGGATCC[C/G]CAGCATTCTACCAAC | 7011 |
rs764978589 | in-del | -/G | 1.70586e-05 | 0.00292045 | intron-variant | TEP1 | GRCh38.p7 | 14:20383679 | AGGGTCAGTGGGAGA[-/G]GAAAAAAAAAGCAGG | 7011 |
rs764985341 | snp | A/C | 3.29533e-05 | 0.00405901 | intron-variant | TEP1 | GRCh38.p7 | 14:20384546 | CAGGTCAGAGCAGGC[A/C]CGGCTCCTCTCACCA | 7011 |
rs764995714 | snp | C/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373312 | GTACAGAACCATCCT[C/T]AGAGGCGGTCAGCAT | 7011 |
rs765003581 | snp | A/G/T | 3.32421e-05 | 0.00407678 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407926 | ATTTCAGGGCTATAG[A/G/T]GCAGGTTGAAAGGTC | 7011 |
rs765014962 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20379439 | TCTCCAGCCTAATGT[A/G]CTATTAGCCTCCCAT | 7011 |
rs765044001 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367733 | CCTGCCTCAGCCTCC[C/T]AAGTAGCTGGGACTA | 7011 |
rs765049221 | snp | A/C/G | 3.30045e-05 | 0.00406219 | intron-variant | TEP1 | GRCh38.p7 | 14:20381419 | GCATGAACAGATATT[A/C/G]AGAAAGGCTCAGCCC | 7011 |
rs765064981 | in-del | -/GT | 1.64789e-05 | 0.0028704 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380278 | TATTAAGCCATCGTA[-/GT]GTGTGTTGGAGGTGC | 7011 |
rs765068996 | snp | A/C | 1.65181e-05 | 0.00287381 | intron-variant | TEP1 | GRCh38.p7 | 14:20377521 | GAGAACAAGGGAGTA[A/C]GACACTTGGGAAGGG | 7011 |
rs765095851 | snp | A/G | 8.40047e-05 | 0.00648038 | intron-variant | TEP1 | GRCh38.p7 | 14:20380072 | GAGAAAGAGTAGGAA[A/G]AAAGGGAGGAAATAA | 7011 |
rs765095872 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366497 | TGGTCCAGAAGGTAT[A/G]TTTCGAGGCTTGGCA | 7011 |
rs765136330 | snp | C/G | 1.95815e-05 | 0.00312896 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383815 | AGGCGTCTGAGCAGA[C/G]TGAGGGCAAGACCCT | 7011 |
rs765144881 | snp | A/C | 1.6531e-05 | 0.00287493 | intron-variant | TEP1 | GRCh38.p7 | 14:20403706 | GGCGTGGGTCGAGGG[A/C]TGGGGCAGTGACTGA | 7011 |
rs765154726 | snp | C/T | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380265 | ATGGTCCGGGGTTTA[C/T]TAAGCCATCGTAGTG | 7011 |
rs765158326 | snp | A/C | 1.65296e-05 | 0.00287481 | intron-variant | TEP1 | GRCh38.p7 | 14:20385125 | CTGCGGGGAGGACAG[A/C]GACAGTGAGTTTAGT | 7011 |
rs765164667 | in-del | -/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20407357 | GTTTTTTGTTGTGTC[-/T]TTTGGGCTTTCATTT | 7011 |
rs765169057 | snp | G/T | 1.66879e-05 | 0.00288855 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386498 | CGGAGGTCGATTCCG[G/T]GAAGGCTGATACGGT | 7011 |
rs765243619 | snp | A/G | 1.65351e-05 | 0.00287528 | intron-variant | TEP1 | GRCh38.p7 | 14:20395953 | GATCACCGACTTCTA[A/G]AAAGCAAAGGAGGGA | 7011 |
rs765260010 | snp | A/T | 0.00212349 | 0.0325152 | intron-variant | TEP1 | GRCh38.p7 | 14:20368794 | CACACACACACACAC[A/T]TACCAGCTGCATACT | 7011 |
rs765270688 | snp | C/T | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380994 | AGTGTGCAGCCACCA[C/T]ATGGAGGTTGGTAAG | 7011 |
rs765291372 | snp | C/G/T | 8.23817e-05 | 0.00641754 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401077 | TCATCCTCTTCCCAG[C/G/T]TCTGCTAGAATCCCA | 7011 |
rs765294692 | snp | C/G | 9.66809e-05 | 0.00695206 | intron-variant | TEP1 | GRCh38.p7 | 14:20396592 | CATCTAGTTGCTGGG[C/G]CCCATGGCTACCAGC | 7011 |
rs765310231 | snp | C/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369530 | TGGGCTGCATTTGGC[C/G]AGGTTCCATAGGATC | 7011 |
rs765312890 | snp | C/T | 3.50779e-05 | 0.0041878 | intron-variant | TEP1 | GRCh38.p7 | 14:20371670 | CAGAGAAAGATCCTA[C/T]TTTAGTTAACCTTTC | 7011 |
rs765313857 | snp | A/T | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377421 | CTGCACCACTCACCA[A/T]TACCTTGGGGCTTAG | 7011 |
rs765323643 | snp | C/G | 1.65345e-05 | 0.00287524 | intron-variant | TEP1 | GRCh38.p7 | 14:20378744 | GACCACTGCAGACCC[C/G]AAGTCTTACCTTTAG | 7011 |
rs765330712 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20378541 | TGTCCCACAGCTGAG[A/G]GAGAGAGAGGAGGAA | 7011 |
rs765332011 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20401396 | TGGGATGGGGGCCAC[A/G]GATGTTGAAAAGTTA | 7011 |
rs765344637 | snp | A/G | 1.65732e-05 | 0.00287859 | intron-variant | TEP1 | GRCh38.p7 | 14:20391781 | GTCTACATGCAAGAA[A/G]GACACAGACACAGGG | 7011 |
rs765360124 | snp | C/G | 0.000486687 | 0.0155919 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384215 | GATGGACACTGGCTG[C/G]TCCAGCAGGGCCCCA | 7011 |
rs765363330 | snp | A/C/G | 3.29654e-05 | 0.00405978 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373091 | CTGCCATGGAACCAT[A/C/G]TGGTGCCCAAGCCAC | 7011 |
rs765373019 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406011 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 7011 |
rs765407018 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20383126 | CCCAGGTCCTCATAG[C/T]TCCCAGATTCACCCC | 7011 |
rs765410027 | in-del | -/A | 3.29451e-05 | 0.00405851 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371283 | ACTCCTTGTGGGTGG[-/A]CAATATCATAGGATT | 7011 |
rs765412735 | snp | A/G | 1.76527e-05 | 0.00297087 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383185 | CAACCTGGTTGTTAA[A/G]TGGTGACTCCTCCAG | 7011 |
rs765420948 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20370100 | TTTATTTTTAGTAAA[G/T]ATGGGGTTTCACCAT | 7011 |
rs765456262 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390715 | AGAGACAGCAGGTAT[C/T]TCCCAAAAGTATTCA | 7011 |
rs765468702 | snp | G/T | 1.98167e-05 | 0.00314769 | intron-variant | TEP1 | GRCh38.p7 | 14:20383673 | GGAAGTCAGGGTCAG[G/T]GGGAGAGAAAAAAAA | 7011 |
rs765483427 | snp | G/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402172 | AATTAGCTGGGCATG[G/T]TGGTGGATGTCTGTA | 7011 |
rs765483843 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20389863 | GTACCTCTCCTGAGA[A/G]CACATAGAATGAGGG | 7011 |
rs765490502 | in-del | -/CCTCTGG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398869 | CTGGAAGCTTTCAGC[-/CCTCTGG]CCTCTGGAAGTCTTG | 7011 |
rs765499232 | snp | G/T | 3.41169e-05 | 0.00413005 | intron-variant | TEP1 | GRCh38.p7 | 14:20379923 | TGCCCCTCCTTGATT[G/T]TCATACCTGCCAAGT | 7011 |
rs765506821 | snp | A/G | 1.80432e-05 | 0.00300354 | intron-variant | TEP1 | GRCh38.p7 | 14:20407822 | GAAAGCTAGAGACAA[A/G]AGCATACAACAGACA | 7011 |
rs765523532 | snp | A/G | 1.6517e-05 | 0.00287372 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382225 | CCCCAAGCACTGACC[A/G]CTCCGTGTGACTTCT | 7011 |
rs765524432 | snp | C/G/T | 5.01268e-05 | 0.00500613 | intron-variant | TEP1 | GRCh38.p7 | 14:20395824 | TATTGTCAGATGTGG[C/G/T]AGGCAAAGAGGAGTT | 7011 |
rs765554021 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394969 | CCTACAAAACAGATG[G/T]TACATCTGTCTTTGA | 7011 |
rs765605601 | snp | C/T | 1.71105e-05 | 0.00292489 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383254 | GGGCCCGAGCAGAGG[C/T]CTCCAGAGGCCCCAA | 7011 |
rs765635088 | in-del | -/C | 1.684e-05 | 0.00290167 | intron-variant, frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404737 | GTTATTGGCCACATT[-/C]CGGACGTTCAGCTGC | 7011 |
rs765676155 | snp | A/T | 1.66857e-05 | 0.00288835 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377741 | GACCCAGAGACCCTG[A/T]CCACACCTGAACCTG | 7011 |
rs765729428 | snp | G/T | 0.000177359 | 0.00941531 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374536 | CACTGGAGCAGGATA[G/T]CTACAGAGTCAGAAG | 7011 |
rs765729508 | snp | C/T | 1.67542e-05 | 0.00289427 | intron-variant | TEP1 | GRCh38.p7 | 14:20377988 | TGCCTTTGCTACTCC[C/T]CCTCACAACCCACCA | 7011 |
rs765733367 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408151 | GGTGGGCAGAAACAT[A/G]TCCATGTGGTTTCTC | 7011 |
rs765764673 | snp | C/T | 1.65255e-05 | 0.00287445 | intron-variant | TEP1 | GRCh38.p7 | 14:20390788 | CTTCATGTTATGTGG[C/T]TGCACAGTAAGCGAC | 7011 |
rs765778906 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401003 | GAGTTCCTCCCAGAC[C/T]GACGCTTTGTTCCCC | 7011 |
rs765786802 | snp | C/T | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408253 | CATATCCATGTGGTT[C/T]TTCCATGGTCTTCAG | 7011 |
rs765792099 | snp | A/G | 4.99646e-05 | 0.00499798 | intron-variant | TEP1 | GRCh38.p7 | 14:20380884 | CCCATAAGCACACCC[A/G]GGAGTCCCATATCTC | 7011 |
rs765794068 | snp | A/C | 3.37798e-05 | 0.00410959 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376263 | CTGCACTGTGAAATC[A/C]TCTGCATTGGAAAAA | 7011 |
rs765810103 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20385333 | AATGCCTGTAATGTA[C/T]TGAGTATTCTGTTAC | 7011 |
rs765829920 | snp | C/T | 1.65526e-05 | 0.00287681 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382285 | AGGCCCGTGCTCCTT[C/T]TCCAGTGTGCTCAGG | 7011 |
rs765835235 | snp | A/G | 0.00014832 | 0.00861035 | intron-variant | TEP1 | GRCh38.p7 | 14:20373433 | GGAGATGGGCTCATG[A/G]GAGTGGGCACAACAG | 7011 |
rs765839762 | snp | C/T | 1.68772e-05 | 0.00290488 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404738 | TTATTGGCCACATTC[C/T]GGACGTTCAGCTGCT | 7011 |
rs765928886 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381591 | TCCTCTAGCCCTGGC[C/T]TCTTCCCATAGCAAC | 7011 |
rs765929050 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408888 | GACATGCCTTCTCAT[A/C]AGAAGGTAAAGGAGA | 7011 |
rs765933376 | snp | A/G | 1.65061e-05 | 0.00287277 | intron-variant | TEP1 | GRCh38.p7 | 14:20387887 | CCAATTCACAAAGGC[A/G]TAGAAACACAGACTG | 7011 |
rs765945105 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398090 | TTTTAAGGTTTATAT[A/C]AATTTTAGGCCGGGT | 7011 |
rs765989117 | snp | A/C/T | 3.33585e-05 | 0.00408391 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401630 | TTTCATCCATGACCA[A/C/T]GGGAACTTTCTTCAA | 7011 |
rs766017661 | snp | C/T | 6.58989e-05 | 0.00573978 | intron-variant | TEP1 | GRCh38.p7 | 14:20371338 | TGAGAAAGGAATAGG[C/T]TGAGCTCAGGATTTA | 7011 |
rs766032612 | in-del | -/AT | 1.6492e-05 | 0.00287154 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381384 | AGGCATCAGCGTCAC[-/AT]GTCTTCCAGAGCTGA | 7011 |
rs766048211 | snp | A/G | 1.67978e-05 | 0.00289804 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395627 | GAAGGAAAGGGCAAT[A/G]CTGTATGATGACAGG | 7011 |
rs766048258 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403412 | GAAACCCTATGTACC[C/T]TGGAAAACATCTGTG | 7011 |
rs766053689 | snp | G/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384635 | CTGTCTGCTTAGGTA[G/T]CTCTTCAGTTCTGAG | 7011 |
rs766068562 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371238 | AAGAAAGAACTCCAG[A/G]ATCCTTGGGCTGCAG | 7011 |
rs766092422 | snp | C/T | 1.64768e-05 | 0.00287021 | intron-variant | TEP1 | GRCh38.p7 | 14:20372700 | GTGAGGAGACTGCTG[C/T]TTCTATCCCATTAAC | 7011 |
rs766105108 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20386786 | TGCTAGTGGTCTCAA[C/T]TGCAGGGCCCTGGAA | 7011 |
rs766127310 | snp | A/G | 1.66974e-05 | 0.00288936 | intron-variant | TEP1 | GRCh38.p7 | 14:20379120 | CCTGCGACAGTGGGT[A/G]AGGGAGCGCAGCTCA | 7011 |
rs766135874 | snp | C/T | 3.2956e-05 | 0.00405918 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386095 | GGAAGTGTGGATGGT[C/T]AGGAAGGTTGTAGCT | 7011 |
rs766172337 | snp | C/T | 1.67066e-05 | 0.00289016 | intron-variant | TEP1 | GRCh38.p7 | 14:20384719 | TGGCACAGAGCTGAC[C/T]ACCAAAGACCCCAAA | 7011 |
rs766192524 | snp | C/T | 1.85941e-05 | 0.00304905 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396690 | CCGCAGCAGGTTGCA[C/T]AGGTTCCGAAGCATG | 7011 |
rs766220012 | snp | A/G | 3.30202e-05 | 0.00406313 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378233 | CTCCGGGTGCCCCCA[A/G]GTCCTACACAGGGAG | 7011 |
rs766237175 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405492 | GGGCAAGTTCACGAC[A/G]GATTTCAAAAATGGC | 7011 |
rs766245587 | snp | C/T | 8.58686e-05 | 0.00655186 | intron-variant | TEP1 | GRCh38.p7 | 14:20391566 | AGCATTCTACCAACC[C/T]AACCCCTTGGAGGAT | 7011 |
rs766250171 | snp | A/G | 0.000263565 | 0.0114766 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380289 | CGTAGTGTGTGTTGG[A/G]GGTGCCATCTCCGGG | 7011 |
rs766263627 | in-del | -/AA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20404356 | TGAAACTCCGTCTCC[-/AA]AAAAAAAAAAAAAAA | 7011 |
rs766280840 | snp | C/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401758 | CAACAAGAGCTCCCA[C/T]GGTAAGCAGCACAGG | 7011 |
rs766300045 | snp | A/C | 2.03552e-05 | 0.00319017 | intron-variant | TEP1 | GRCh38.p7 | 14:20383957 | CATGGTCACATTTTA[A/C]ATGCCTGAGCTCCCT | 7011 |
rs766303079 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380376 | TGGGGCAGGAGCCGG[A/G]GGTACTGGCTGAGGA | 7011 |
rs766317083 | snp | A/C | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384494 | GCTGCCACACCCCCC[A/C]ACTCACAGGGGTATC | 7011 |
rs766351451 | snp | A/C | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382664 | GGTGATCGGTGACCA[A/C]GCGCAGGTAGAGCGG | 7011 |
rs766426178 | in-del | -/AA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20383681 | GGGTCAGTGGGAGAG[-/AA]AAAAAAAGCAGGGGT | 7011 |
rs766426774 | snp | C/T | 3.29723e-05 | 0.00406018 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377438 | ACCTTGGGGCTTAGC[C/T]AGGCCAGGGCGGACA | 7011 |
rs766433247 | in-del | -/C | 0.000236173 | 0.0108642 | intron-variant | TEP1 | GRCh38.p7 | 14:20374398 | TAGCCCTTCCAGAGA[-/C]CCCCCAGTGGGATCT | 7011 |
rs766453939 | snp | A/G | 8.27205e-05 | 0.00643066 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373786 | TCAAGGTCCCATCCC[A/G]GCTCACAGACACCAC | 7011 |
rs766463039 | snp | C/G | | | | | GRCh38.p7 | 14:20415600 | CGGGCATGGTGGTGG[C/G]CGCCTGTAATCCCAG | 7011 |
rs766474691 | snp | A/G | 1.65154e-05 | 0.00287358 | intron-variant | TEP1 | GRCh38.p7 | 14:20377541 | CTTGGGAAGGGGTAG[A/G]GGGCAGGGGCTGCGC | 7011 |
rs766482594 | snp | A/C | 1.80426e-05 | 0.00300349 | intron-variant | TEP1 | GRCh38.p7 | 14:20407829 | AGAGACAAGAGCATA[A/C]AACAGACATGGCTGG | 7011 |
rs766485108 | snp | A/C | 1.66701e-05 | 0.002887 | intron-variant | TEP1 | GRCh38.p7 | 14:20389588 | ATTTCTGACACTGGG[A/C]AGGAAGTATAAGCAC | 7011 |
rs766514212 | in-del | -/G | | | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365404 | TCAGCCCCCCAAGTA[-/G]CTGGGATTACAGGTG | 7011 |
rs766537814 | snp | C/T | 1.65288e-05 | 0.00287474 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407940 | GGGCAGGTTGAAAGG[C/T]CTAGTCCCTTAGAGA | 7011 |
rs766538415 | snp | C/T | 1.65397e-05 | 0.00287569 | intron-variant | TEP1 | GRCh38.p7 | 14:20385131 | GGAGGACAGAGACAG[C/T]GAGTTTAGTCCTAGG | 7011 |
rs766561977 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394913 | AAATAAGTGTAAGAT[A/G]CTGATGAACCACTTA | 7011 |
rs766573990 | snp | A/C | 3.30109e-05 | 0.00406256 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381939 | CTGGACGAGGCAGGC[A/C]AACGGGCCCATGGGG | 7011 |
rs766578304 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20381885 | AGGCACAGAGAGGTC[A/C]GCGGGAGCTCTGCTG | 7011 |
rs766596970 | in-del | -/C | 1.64727e-05 | 0.00286986 | frameshift-variant, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372759 | GGGTGCCGAACCCTT[-/C]CGCAGTTTCACTTGC | 7011 |
rs766609831 | snp | A/T | 1.65866e-05 | 0.00287976 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382296 | CCTTCTCCAGTGTGC[A/T]CAGGATGTGCTGCAG | 7011 |
rs766624751 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403769 | TTGGCCCGGTGCTTC[C/T]GAGGGTTGTACTTAG | 7011 |
rs766638741 | snp | C/G | 1.64974e-05 | 0.00287201 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378103 | AAGCCATGGTGGGCA[C/G]GGAAGGCAGCCAGCC | 7011 |
rs766653189 | snp | C/T | 1.65367e-05 | 0.00287543 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389712 | ATTCCATCATCCATG[C/T]TTTGGCCAAGGAGGA | 7011 |
rs766660558 | snp | C/T | 1.69784e-05 | 0.00291357 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386464 | GTTCCTACGGGTCTC[C/T]TCCTCAGTGACGCCC | 7011 |
rs766660580 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391016 | AGTCTTCAGAGTGTC[A/G]CCTCCACACAGCACG | 7011 |
rs766680443 | snp | A/G | 1.64904e-05 | 0.00287139 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395520 | TCCTCATTGCCATCC[A/G]AAGCTGCTGACGGCT | 7011 |
rs766720048 | snp | A/G/T | 0.000186694 | 0.00965992 | intron-variant, missense, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404743 | GGCCACATTCCGGAC[A/G/T]TTCAGCTGCTGCCTG | 7011 |
rs766727831 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373545 | TGGCCCCATCTAGCC[C/T]GACGGTTACCACCAG | 7011 |
rs766744376 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375230 | CAGGCTGGAGTGCAA[C/T]GGCGCGACCTCTGCC | 7011 |
rs766768416 | snp | C/T | 1.64963e-05 | 0.00287192 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382008 | CCAGCTCTTAGTCCC[C/T]TTCGGTAGTGTCCGC | 7011 |
rs766775956 | snp | A/C | 1.79774e-05 | 0.00299806 | intron-variant | TEP1 | GRCh38.p7 | 14:20382384 | GAGGACAGCCTTGTT[A/C]AGTGCAGTGGGAGGA | 7011 |
rs766780868 | in-del | -/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408909 | GTAAAGGAGACCCAA[-/C]CCCCCTGACCCCCGC | 7011 |
rs766833211 | snp | C/G | 1.65773e-05 | 0.00287895 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408405 | AAGGAGAGGATGTCT[C/G]GATGGGCAGACACAT | 7011 |
rs766836787 | snp | A/G | 1.6832e-05 | 0.00290099 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375757 | GCCCTTTACTCACCA[A/G]TAGGTTATCTTTGGT | 7011 |
rs766861995 | snp | A/C/T | 0.000111108 | 0.00745278 | intron-variant | TEP1 | GRCh38.p7 | 14:20404816 | CTCAGTCACTCCTCC[A/C/T]GTAGCTTTCTGCCCT | 7011 |
rs766882654 | snp | G/T | 0.000115322 | 0.00759261 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406297 | TCTCCAGAGGTGAGC[G/T]TCACGGCCAGATCCT | 7011 |
rs766889772 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | TEP1 | GRCh38.p7 | 14:20375899 | GGAGAGGGAGCAATC[A/G]GGACCAAAGGAAGGA | 7011 |
rs766906583 | snp | A/G | 3.29946e-05 | 0.00406155 | intron-variant | TEP1 | GRCh38.p7 | 14:20369644 | CCTGGGCCATCTCCC[A/G]GCTCCTCAGGTCCTC | 7011 |
rs766909256 | snp | A/G | 1.68221e-05 | 0.00290014 | intron-variant | TEP1 | GRCh38.p7 | 14:20379140 | AGCGCAGCTCAGGCC[A/G]TCCCCTTGACCCTCC | 7011 |
rs766925297 | in-del | -/AA | 1.70743e-05 | 0.00292179 | intron-variant | TEP1 | GRCh38.p7 | 14:20405616 | GAGGGAAGAAATGAG[-/AA]GAGAGGTAACAAGGA | 7011 |
rs766940783 | snp | C/T | 1.65141e-05 | 0.00287346 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378777 | ATCCTCCCAAGCACA[C/T]GGTGGCTAGCAGCCG | 7011 |
rs766967770 | snp | A/G | 1.64914e-05 | 0.00287149 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401104 | CCCAAGGCCCAGGAA[A/G]GCGACTTCGAGAAAA | 7011 |
rs766969087 | snp | A/G | 3.29609e-05 | 0.00405948 | intron-variant | TEP1 | GRCh38.p7 | 14:20371360 | CAGGATTTAAAGAGA[A/G]GTAAAGAGAAGAACA | 7011 |
rs766972375 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant | TEP1 | GRCh38.p7 | 14:20381271 | TCAGAGCAACCAAAG[C/T]ACTCACTTTGGGAAA | 7011 |
rs766986957 | in-del | -/TCT | 4.98016e-05 | 0.00498982 | intron-variant | TEP1 | GRCh38.p7 | 14:20388084 | TAAATAACAAGATAA[-/TCT]ATGAGAGTAGAATAC | 7011 |
rs766992700 | snp | C/T | 3.33161e-05 | 0.00408129 | intron-variant | TEP1 | GRCh38.p7 | 14:20388099 | AATGAGAGTAGAATA[C/T]CACAGGTCGAAATCA | 7011 |
rs767000457 | snp | C/T | 1.79935e-05 | 0.00299941 | intron-variant | TEP1 | GRCh38.p7 | 14:20401173 | AAGAGGTCTATCATT[C/T]CAGAGTCAGCAAGAA | 7011 |
rs767020794 | snp | C/T | 1.66026e-05 | 0.00288115 | intron-variant | TEP1 | GRCh38.p7 | 14:20391790 | CAAGAAAGACACAGA[C/T]ACAGGGGCTCAGGGA | 7011 |
rs767042618 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20396064 | CAAAATGAACTTAGA[C/T]AAGAGATATAGAAAA | 7011 |
rs767045035 | snp | A/G | 0.000412082 | 0.0143482 | intron-variant | TEP1 | GRCh38.p7 | 14:20373164 | TGGAGGAGAAAGGAC[A/G]TGTTTCATTAGGAGC | 7011 |
rs767049887 | in-del | -/G | 0.000115908 | 0.00761188 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383855 | GAGCCCCAGAAAAGT[-/G]GAAGAAGACTAATGA | 7011 |
rs767077979 | snp | G/T | 1.68616e-05 | 0.00290353 | intron-variant | TEP1 | GRCh38.p7 | 14:20384740 | AGACCCCAAAAGTTG[G/T]AATAGACTCAGACCC | 7011 |
rs767088807 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20407498 | GATGCGTGCCACCAC[A/C]CCTGGCTAATTTTTG | 7011 |
rs767100832 | snp | C/T | 6.59348e-05 | 0.00574135 | intron-variant | TEP1 | GRCh38.p7 | 14:20373667 | AGGGGAGGTGGCTGA[C/T]GTTTTGTTACCTGCA | 7011 |
rs767109656 | snp | A/C | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395923 | AAGAAATCTGAATGG[A/C]AACTGCCGACTGTGG | 7011 |
rs767125326 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403425 | CCTTGGAAAACATCT[A/G]TGAGAAAATGGAGGC | 7011 |
rs767198042 | snp | C/T | 1.64895e-05 | 0.00287132 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368467 | AAAGTACACATTGCC[C/T]TGCACGTCTCCCACG | 7011 |
rs767203732 | in-del | -/AAAAAA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410021 | GCAAGACTCTGTCTC[-/AAAAAA]AAAAAAAAAAAAAAA | 7011 |
rs767244073 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371549 | AAATCTGCTTTGGCC[A/G]AGATGAGAAAGTGAC | 7011 |
rs767270300 | snp | A/G | 0.000166514 | 0.00912301 | intron-variant | TEP1 | GRCh38.p7 | 14:20383682 | GGTCAGTGGGAGAGA[A/G]AAAAAAAGCAGGGGT | 7011 |
rs767272386 | snp | A/G | 6.60764e-05 | 0.00574751 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385004 | GGAAGCTGGAATCCC[A/G]GAAGTAGATGAGAGC | 7011 |
rs767287047 | snp | C/T | 4.94368e-05 | 0.00497152 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369357 | ACCTTTCTACGCTGC[C/T]GTGTCTTTAGATGTG | 7011 |
rs767300385 | snp | G/T | 1.65274e-05 | 0.00287462 | intron-variant | TEP1 | GRCh38.p7 | 14:20382719 | CAGCAGTCGCATCTG[G/T]CAAGACTCAGGACTC | 7011 |
rs767308090 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20390583 | CTGACTATTGTATGT[G/T]GTTGGAGAAGTCAGC | 7011 |
rs767317862 | snp | A/G | 1.6902e-05 | 0.00290701 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380469 | TCCTCTTTGGGGACT[A/G]AAGAAGCTATAAAAG | 7011 |
rs767325258 | snp | A/T | 2.01786e-05 | 0.0031763 | intron-variant | TEP1 | GRCh38.p7 | 14:20383735 | TGGGCTCATTGGGGG[A/T]TACCCACCGGTAGGT | 7011 |
rs767357247 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403342 | CCAGAAGAGATTGTA[C/T]ATGCACATATACAAC | 7011 |
rs767361602 | snp | A/G | 3.30677e-05 | 0.00406605 | intron-variant | TEP1 | GRCh38.p7 | 14:20400957 | GGGGAAGAGAAGGAG[A/G]GAATGTGATGGTCAA | 7011 |
rs767374787 | snp | C/T | 1.69847e-05 | 0.00291411 | intron-variant | TEP1 | GRCh38.p7 | 14:20376270 | GTGAAATCCTCTGCA[C/T]TGGAAAAAGAGAGAG | 7011 |
rs767385567 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387982 | GACCCCTGTCTTTCC[C/T]GGGGGTGGTGGAATC | 7011 |
rs767396948 | snp | A/G | 4.94515e-05 | 0.00497225 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378384 | GACCTTCTTACCTTG[A/G]TGACTTTGAGCCCAT | 7011 |
rs767407389 | snp | C/G/T | 3.33052e-05 | 0.00408065 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391599 | TTTTTGTTTTCTTAC[C/G/T]CCTTGTGGGTTGCTC | 7011 |
rs767447795 | snp | C/G | 1.65302e-05 | 0.00287486 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378494 | CAGGGACTTGGGGTA[C/G]GTGTGCTGGAAGGCC | 7011 |
rs767496059 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393369 | TAGCAAAATCAGTAG[A/T]CTTCCCAGCACTATC | 7011 |
rs767501086 | snp | C/T | 1.73643e-05 | 0.0029465 | intron-variant | TEP1 | GRCh38.p7 | 14:20377274 | CTGCCCACTGTCTAG[C/T]AGTACCTGAGGCAGA | 7011 |
rs767504650 | snp | A/C/T | 0.000110332 | 0.00742672 | intron-variant | TEP1 | GRCh38.p7 | 14:20383152 | ACCCCACACACCCAC[A/C/T]GGCCCCGGCCTAGAA | 7011 |
rs767504797 | snp | C/T | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381603 | GGCCTCTTCCCATAG[C/T]AACGTTTAGCTGCTG | 7011 |
rs767513163 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376595 | CCAGTGTCACTTCCA[C/T]CTCGTGACCTGTGAG | 7011 |
rs767529565 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403160 | GCATAACTTCATCTC[-/AAA]AAAAAAAAAAAAAAA | 7011 |
rs767536719 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408029 | GTACAAATCAGCTTG[C/T]GTCATGTGAGATATC | 7011 |
rs767549589 | snp | C/T | 1.65452e-05 | 0.00287616 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383547 | TCTGGTCCACTAACC[C/T]ATCAGCCCCATCGAT | 7011 |
rs767578551 | snp | C/T | 4.94246e-05 | 0.0049709 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406301 | CAGAGGTGAGCTTCA[C/T]GGCCAGATCCTCCAC | 7011 |
rs767583635 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20380784 | AGAGTCACGTGCTCA[C/T]CCTCTTGGCATTTTC | 7011 |
rs767589651 | snp | A/C/G | 3.29974e-05 | 0.00406175 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382013 | TCTTAGTCCCCTTCG[A/C/G]TAGTGTCCGCCACAC | 7011 |
rs767617934 | snp | C/T | 3.29495e-05 | 0.00405877 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377640 | GCCATCCGCTCGATA[C/T]CCAACAGCCACCCGA | 7011 |
rs767618109 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392354 | AGATTAGGCTATTAC[C/T]ACCTAGAAGTGCTGA | 7011 |
rs767620487 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386111 | AGGAAGGTTGTAGCT[A/G]GGGGGAATGTATCCA | 7011 |
rs767622251 | snp | C/G | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407960 | TCCCTTAGAGAAATG[C/G]TGAGCCCTCCAACTT | 7011 |
rs767625489 | snp | C/G | 3.29451e-05 | 0.00405851 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403785 | GAGGGTTGTACTTAG[C/G]CAGCTGGTACTCGTC | 7011 |
rs767636064 | snp | C/T | 3.31735e-05 | 0.00407255 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389737 | GGAGGATGACCCTGT[C/T]CACCTGTAAGATGAA | 7011 |
rs767669514 | snp | C/G | 1.80282e-05 | 0.0030023 | intron-variant | TEP1 | GRCh38.p7 | 14:20384008 | ACACAGCCTTCCCTC[C/G]CTCCTGCCCAGGCCC | 7011 |
rs767674334 | snp | C/G | 1.7243e-05 | 0.00293619 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374494 | GCCGCTGTCCTGACT[C/G]TGGGTCCCAGAGCCC | 7011 |
rs767678509 | snp | C/G | 1.64803e-05 | 0.00287052 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403855 | GGCGGGCAGGGGCAC[C/G]AGCTTATTCTTATCT | 7011 |
rs767694405 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380396 | CTGGCTGAGGATTGA[A/G]GCCTGCTGCCTCAGG | 7011 |
rs767714867 | snp | A/G | 1.74254e-05 | 0.00295168 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386579 | TCCCGCTCCCCATGC[A/G]TGTCTCGGAAAGTGG | 7011 |
rs767738893 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374025 | CATGCTCTCCTCTCT[C/T]CCTTTACACCAACCC | 7011 |
rs767751524 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409501 | TCCCCGTTGGACATC[C/T]CCACTGGATGACTCA | 7011 |
rs767765702 | snp | A/T | 4.98078e-05 | 0.00499013 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376121 | GATCCCGGCCCCCGG[A/T]GGCCAGGCTGCCTCC | 7011 |
rs767778631 | snp | A/T | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372798 | GATTTTCTCATCAGC[A/T]CTGAGGACAAAAAAG | 7011 |
rs767790509 | snp | C/T | 1.64808e-05 | 0.00287057 | intron-variant | TEP1 | GRCh38.p7 | 14:20378868 | CCTATCCCAGGAAGA[C/T]GAAGTCAGTCCTCTG | 7011 |
rs767809211 | snp | C/T | 3.29478e-05 | 0.00405867 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384423 | GGATCATATTCCATA[C/T]ATCCTGCAGAACCAA | 7011 |
rs767820333 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | TEP1 | GRCh38.p7 | 14:20386201 | TTCCAGTTGTCTGTA[A/G]GCATGATGATAGGGA | 7011 |
rs767838680 | snp | A/G | 1.64993e-05 | 0.00287218 | intron-variant | TEP1 | GRCh38.p7 | 14:20390668 | AGAGGGTTTCTCAGG[A/G]ATTAATACTCACAGG | 7011 |
rs767839931 | snp | C/T | 0.000131132 | 0.00809621 | intron-variant | TEP1 | GRCh38.p7 | 14:20401183 | TCATTTCAGAGTCAG[C/T]AAGAAAATAACTCAG | 7011 |
rs767924491 | snp | A/G | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413703 | GTCCTATTTTCTCCT[A/G]TCCCTAGGGCTTCCC | 7011 |
rs767959472 | snp | C/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381316 | CTAGGAACTAACCAG[C/G]TGGTAAGGCAGGTCT | 7011 |
rs767971195 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388343 | GGGGTAGGGAAAGGT[A/G]TAAAGATTAAAGCCA | 7011 |
rs767994967 | snp | G/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405483 | GCTCCAGGAGGGCAA[G/T]TTCACGACAGATTTC | 7011 |
rs768000919 | snp | C/T | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379017 | CAGAGCTCCAGGAGC[C/T]CGTCGAAGGCAGTAA | 7011 |
rs768014779 | snp | A/G | 8.25021e-05 | 0.00642217 | intron-variant | TEP1 | GRCh38.p7 | 14:20381413 | TGAGCTGCATGAACA[A/G]ATATTGAGAAAGGCT | 7011 |
rs768060412 | snp | A/C | 1.65976e-05 | 0.00288072 | intron-variant | TEP1 | GRCh38.p7 | 14:20386059 | CCCAGCCCTCCTCCA[A/C]ACCTGTCTGCCTTAC | 7011 |
rs768074751 | snp | C/T | 3.30366e-05 | 0.00406413 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382037 | GCCACACACTCAGCA[C/T]TCCGTGCAGCTGGTC | 7011 |
rs768105495 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408005 | CAGGCAATTGCTGTT[A/G]TTCACACGGTACAAA | 7011 |
rs768108316 | snp | A/G | 1.65072e-05 | 0.00287286 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389684 | CCAGTAAAGCTGTTT[A/G]GCCACATTTATCATT | 7011 |
rs768121704 | snp | A/T | 3.35785e-05 | 0.00409733 | intron-variant | TEP1 | GRCh38.p7 | 14:20383442 | GTGCCGTATCCCTCC[A/T]TCTCCCCAGCCTGCC | 7011 |
rs768131285 | snp | A/C/T | 3.29469e-05 | 0.00405864 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20371217 | CTCAAATAGGACTTA[A/C/T]CAAGAAAGAAAGAAC | 7011 |
rs768184396 | snp | C/G | 8.26549e-05 | 0.00642811 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369778 | CCTGATTCCTTTTGC[C/G]TCTGTGAAAGAATAG | 7011 |
rs768190131 | in-del | -/T | 1.69135e-05 | 0.002908 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408430 | CACATGCCCATGGAG[-/T]TTTTTCCATGGCTGA | 7011 |
rs768190702 | snp | A/G | 1.64966e-05 | 0.00287194 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381975 | GTCTCCACTGTTACC[A/G]GCAGCCACTGCTTCT | 7011 |
rs768232222 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372755 | TTCCGGGTGCCGAAC[A/C]CTTCCGCAGTTTCAC | 7011 |
rs768252554 | snp | C/T | 1.93179e-05 | 0.00310782 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383896 | GCCCCATCAGGAGCC[C/T]GCAGGGCTGACACAA | 7011 |
rs768280501 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377609 | CAGTACCTGAAGAGA[C/T]TTTGTAGATCCTAAT | 7011 |
rs768292420 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20390513 | TCTAGGCAGCTGGTT[A/G]TTAGATATTCAGCAG | 7011 |
rs768302726 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398582 | CCTCAACTATTACAC[A/G]TAACACATAACACTG | 7011 |
rs768314089 | snp | C/G/T | 0.000121826 | 0.00780381 | intron-variant | TEP1 | GRCh38.p7 | 14:20381084 | TTAGGGATATGAAGG[C/G/T]GCTGGTGAGAAGGGA | 7011 |
rs768333328 | snp | A/T | 8.39285e-05 | 0.00647744 | intron-variant | TEP1 | GRCh38.p7 | 14:20373841 | AAGATCAGAGCAGAG[A/T]CATATTGAGCAGGAC | 7011 |
rs768341661 | snp | G/T | 6.60437e-05 | 0.00574608 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403748 | GGTGGCCGGCGGGGG[G/T]GTCTCTTGGCCCGGT | 7011 |
rs768350963 | snp | A/C | 8.47939e-05 | 0.00651074 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383243 | TCTCACCAGCCGGGC[A/C]CGAGCAGAGGCCTCC | 7011 |
rs768369062 | snp | A/G | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378821 | AGGCAGCAGCCAGTG[A/G]TTTGGTACTGGTGAG | 7011 |
rs768369430 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411444 | ACTTCAGTTTCATCA[A/C]CTCCTCCAAAAAGCC | 7011 |
rs768380289 | snp | C/T | | | splice-acceptor-variant | TEP1 | GRCh38.p7 | 14:20377493 | GAGCCCCCTGGGAAC[C/T]TAGAGAATGAGAGAG | 7011 |
rs768380701 | snp | C/T | 4.98575e-05 | 0.00499262 | splice-acceptor-variant | TEP1 | GRCh38.p7 | 14:20391098 | TAGTTCAGCGGGGGC[C/T]GATTGGACAAGTGTC | 7011 |
rs768388925 | snp | C/T | 8.23662e-05 | 0.00641688 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403824 | CAAATTTGTCCGTCA[C/T]GGCAGTACGGAGACA | 7011 |
rs768391806 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20382514 | ATGAGGCGAGGATAG[A/G]GAGTGGGTGATCACA | 7011 |
rs768466652 | snp | A/G | 1.71264e-05 | 0.00292624 | intron-variant | TEP1 | GRCh38.p7 | 14:20381709 | CGTGTGAGGAAGGGA[A/G]AGAGAAGAAGGAAGA | 7011 |
rs768511166 | snp | C/T | 0.000346652 | 0.0131608 | intron-variant | TEP1 | GRCh38.p7 | 14:20369626 | CAGGGATCTGCCATC[C/T]ACCCTGGGCCATCTC | 7011 |
rs768531497 | snp | A/G | 1.64825e-05 | 0.00287071 | intron-variant | TEP1 | GRCh38.p7 | 14:20384344 | AGGACAACCCAGACC[A/G]CCCCATGTCCCTCTC | 7011 |
rs768533512 | snp | C/T | 1.66874e-05 | 0.0028885 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386542 | GGCCTGCAGTGCTGG[C/T]AGCACAGACCTCAGC | 7011 |
rs768553449 | snp | A/G | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368510 | GTGGAGTTAGCGCCC[A/G]GCCAAGGTTCCAGGC | 7011 |
rs768563504 | snp | C/T | 1.65124e-05 | 0.00287331 | intron-variant | TEP1 | GRCh38.p7 | 14:20390778 | AGGAAAGAGACTTCA[C/T]GTTATGTGGTTGCAC | 7011 |
rs768563629 | in-del | -/C | 6.67668e-05 | 0.00577745 | intron-variant | TEP1 | GRCh38.p7 | 14:20391814 | TCAGGGACTTATCTG[-/C]CCCTTAGAGGCAGAC | 7011 |
rs768574728 | snp | C/T | 1.72305e-05 | 0.00293513 | intron-variant | TEP1 | GRCh38.p7 | 14:20395422 | GCCCCGATTGCCCAC[C/T]CTTGGCTCCCAGACA | 7011 |
rs768585720 | snp | C/T | 3.34001e-05 | 0.00408643 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386496 | AGCGGAGGTCGATTC[C/T]GTGAAGGCTGATACG | 7011 |
rs768609519 | snp | A/G | 0.000164747 | 0.0090745 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369700 | TTGGCTTGAGTTATC[A/G]ATATTAGGGTCCTAC | 7011 |
rs768621849 | snp | C/T | 8.26385e-05 | 0.00642747 | intron-variant | TEP1 | GRCh38.p7 | 14:20389330 | AGTCATTAACCATCA[C/T]AAACAATACCTGGAA | 7011 |
rs768627842 | snp | A/C/T | 8.25068e-05 | 0.00642241 | synonymous-codon, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395506 | ATACAACACAGGTAT[A/C/T]CTCATTGCCATCCGA | 7011 |
rs768634291 | snp | C/T | 1.65518e-05 | 0.00287674 | intron-variant | TEP1 | GRCh38.p7 | 14:20401437 | TAGATGGAATGCATG[C/T]TCAGGGTGCAGCTTC | 7011 |
rs768661571 | snp | C/G | 1.78752e-05 | 0.00298953 | intron-variant | TEP1 | GRCh38.p7 | 14:20375716 | GTCTTGCCCCAGGAA[C/G]CCAGCTGGGCTCTGT | 7011 |
rs768661847 | snp | A/C | 1.65116e-05 | 0.00287324 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377492 | TGAGCCCCCTGGGAA[A/C]CTAGAGAATGAGAGA | 7011 |
rs768681029 | snp | C/G | 2.04167e-05 | 0.00319499 | intron-variant | TEP1 | GRCh38.p7 | 14:20383718 | GTGGGCATCAACAAG[C/G]CTGGGCTCATTGGGG | 7011 |
rs768687437 | in-del | -/C | 4.98442e-05 | 0.00499196 | intron-variant | TEP1 | GRCh38.p7 | 14:20391798 | ACACAGACACAGGGG[-/C]TCAGGGACTTATCTG | 7011 |
rs768691662 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20412802 | TAACTGGGATTACAG[G/T]CGCCCACCACCATGC | 7011 |
rs768693365 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20399066 | CCAGCTAATTTTTCT[A/G]TTTTTGGTTAGAGAC | 7011 |
rs768706165 | snp | C/T | 1.82164e-05 | 0.00301793 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383320 | TCTCCCCTAGGCCTG[C/T]ATCACTAGACACACT | 7011 |
rs768712036 | snp | A/G | 3.2963e-05 | 0.00405961 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395901 | CATCAATGGCATCAT[A/G]GGCGTTAAGAAATCT | 7011 |
rs768765678 | snp | C/T | 3.33723e-05 | 0.00408473 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376105 | CTTCTGCAGCTCACC[C/T]GATCCCGGCCCCCGG | 7011 |
rs768794902 | snp | G/T | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373393 | CCAGGAGGGTGTGGG[G/T]TTGGCACACCTAGGA | 7011 |
rs768798273 | snp | A/C | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403032 | CGTGGTGGCACACGC[A/C]TGTAGTCCCAGCTAT | 7011 |
rs768846259 | snp | A/G | 4.95381e-05 | 0.0049766 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380022 | AGGCCACAGCAGTAG[A/G]GGATGAGGAAACTGC | 7011 |
rs768857084 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374591 | CCCTCCAGCATTTTG[C/G]TATATCTGTAGTGTA | 7011 |
rs768898185 | snp | C/T | 3.34185e-05 | 0.00408756 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404726 | ATGGCCAAGATGTTA[C/T]TGGCCACATTCCGGA | 7011 |
rs768910793 | snp | A/G | 4.96454e-05 | 0.00498199 | intron-variant | TEP1 | GRCh38.p7 | 14:20388071 | CAATGAACCTGACAT[A/G]AATAACAAGATAAAT | 7011 |
rs768916812 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373138 | GAACTCCTTGGTATA[C/T]ATGTGTCATCTGGAG | 7011 |
rs768920792 | snp | A/G | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390947 | TCTGACCTGGACTTG[A/G]GCCTGGAGCTTGATG | 7011 |
rs768942988 | in-del | -/C/GC | 0.000121059 | 0.00777913 | intron-variant | TEP1 | GRCh38.p7 | 14:20386437 | CCCTCTTCTCTGCAG[-/C/GC]CCCCCACACCTGTTC | 7011 |
rs768959051 | snp | A/G | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373512 | AGGAACTCACCAAGA[A/G]TGGATGCCATAACCG | 7011 |
rs768973014 | snp | C/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408346 | GCTGATGTAGTTTCT[C/G]CAAGGGCTGTAAGTC | 7011 |
rs768990276 | snp | A/C | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380978 | ACCAGACCCAATTCC[A/C]AGTGTGCAGCCACCA | 7011 |
rs769006109 | snp | A/G | 0.00815947 | 0.0633495 | intron-variant | TEP1 | GRCh38.p7 | 14:20377230 | TAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAACAG | 7011 |
rs769009869 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20396904 | TCTCAAAAAAAAAAA[C/G]CAAATGAGGGATGAT | 7011 |
rs769020744 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387958 | CTCTTCCAGTGGCCG[A/G]AGAGACTGGACCCCT | 7011 |
rs769029457 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371498 | TCTTACCAGATTTCA[C/G]ATGGAGCATCCCCTG | 7011 |
rs769063052 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406257 | CTGAAGGACATGGTC[A/G]GTAGGCTCTGGATGA | 7011 |
rs769064357 | snp | A/G | 6.70062e-05 | 0.0057878 | intron-variant | TEP1 | GRCh38.p7 | 14:20395810 | GCTGCTGCTTCATTT[A/G]TTGTCAGATGTGGGA | 7011 |
rs769080917 | in-del | -/T | 1.67984e-05 | 0.00289809 | intron-variant | TEP1 | GRCh38.p7 | 14:20369809 | TAATTTTGTTTAGCC[-/T]TACCCATATGAGTCA | 7011 |
rs769112190 | snp | A/G | 3.29565e-05 | 0.00405921 | intron-variant | TEP1 | GRCh38.p7 | 14:20373620 | GTCAGAAGAAGGGAC[A/G]GAGCAGGGGAGAAAA | 7011 |
rs769119746 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20378683 | CAGCCTCTGCCGCAC[C/T]GAGAGAACAAATTCA | 7011 |
rs769120454 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403405 | TCTCTGAGAAACCCT[A/G]TGTACCTTGGAAAAC | 7011 |
rs769127138 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366124 | AACAATTATACCATG[A/T]CCTCACTGTCCTTCT | 7011 |
rs769127499 | snp | A/C | 1.66324e-05 | 0.00288374 | intron-variant | TEP1 | GRCh38.p7 | 14:20403931 | CAAGACCCAAACCAA[A/C]CCTCCAAAACAAAAC | 7011 |
rs769169544 | snp | C/T | 1.66065e-05 | 0.00288149 | intron-variant | TEP1 | GRCh38.p7 | 14:20403675 | CTCCCTTGTCCTGCC[C/T]TTCCTGGAGAAAAGG | 7011 |
rs769207798 | in-del | -/AAG | 3.2956e-05 | 0.00405918 | intron-variant | TEP1 | GRCh38.p7 | 14:20373634 | CGGAGCAGGGGAGAA[-/AAG]AAGAGACAGCAGGGA | 7011 |
rs769209529 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20377045 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 7011 |
rs769221526 | snp | C/T | 1.66051e-05 | 0.00288137 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380448 | TCAGCCTCGGGGAGC[C/T]TTTGTTCCTCTTTGG | 7011 |
rs769241251 | snp | A/C | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386150 | GCCCAGAATCCCCAC[A/C]AACAGCTGTGCGTTC | 7011 |
rs769243730 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371309 | GGATTTTCTGTATAG[C/T]TGCTCCTGGTTTGTG | 7011 |
rs769286879 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388877 | AACTGGAGCCGGGTG[C/T]GGTGGCTCACGCCTG | 7011 |
rs769359774 | snp | A/C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369505 | TGTTACCTGTGGTCC[A/C/G]TTCTCCTTCTGGGCT | 7011 |
rs769367433 | snp | C/G/T | 3.54498e-05 | 0.00420998 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396676 | GAACTGATTCCAACC[C/G/T]GCAGCAGGTTGCACA | 7011 |
rs769378321 | snp | A/G | 1.65067e-05 | 0.00287282 | intron-variant | TEP1 | GRCh38.p7 | 14:20378337 | CCACCCTCCACTCCT[A/G]TCCTCCTGTGCTTCC | 7011 |
rs769391051 | snp | C/T | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382700 | CTGATTCCCGCTTCA[C/T]CAGCAGCAGTCGCAT | 7011 |
rs769393531 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402158 | AAAACTACAAAAAAA[-/G]TTAGCTGGGCATGGT | 7011 |
rs769409744 | snp | A/G | 1.72314e-05 | 0.0029352 | intron-variant | TEP1 | GRCh38.p7 | 14:20369831 | TATGAGTCAACTTGT[A/G]CCAGACAAAACAACA | 7011 |
rs769412334 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411353 | TGTGCACAGGCAGAT[C/T]CCTGGAACACTCTTT | 7011 |
rs769430425 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400927 | AGTGAGGATCTAAAA[C/T]GTGGAGGCATAAATG | 7011 |
rs769436134 | snp | A/T | 1.64768e-05 | 0.00287021 | intron-variant | TEP1 | GRCh38.p7 | 14:20384570 | CTCACCACATCTCTG[A/T]ACAGGTGCTCCCTAC | 7011 |
rs769458456 | in-del | -/TTAAAC | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393414 | TACAATTAAATCAAA[-/TTAAAC]TTAAATTATACACAT | 7011 |
rs769476240 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20412554 | ATGCAAATACATGCC[G/T]TCACCATCACCACTG | 7011 |
rs769476891 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405020 | CAACCAGGCCTTTTC[C/T]TTCTTTGGAAGACCT | 7011 |
rs769492613 | snp | A/G | 4.95127e-05 | 0.00497533 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384139 | GAAGAAGGCGTGGCC[A/G]GGCAGGACTCGGTGG | 7011 |
rs769519835 | snp | C/T | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377624 | TTTTGTAGATCCTAA[C/T]GCCATCCGCTCGATA | 7011 |
rs769549446 | snp | C/T | | | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369437 | TTCCCTGCAGGTAGA[C/T]GGGTCTGTCCCTGGA | 7011 |
rs769561907 | snp | A/G | 0.000151665 | 0.00870685 | intron-variant | TEP1 | GRCh38.p7 | 14:20396772 | AAAAACAAATGAGAA[A/G]GCCAGGCACAGTGGC | 7011 |
rs769567054 | snp | A/C | 1.64933e-05 | 0.00287165 | intron-variant | TEP1 | GRCh38.p7 | 14:20378974 | ACAAATGGGGAGGAC[A/C]CCTTACCGACAACCA | 7011 |
rs769569620 | snp | A/C/T | 0.00013502 | 0.00821542 | intron-variant | TEP1 | GRCh38.p7 | 14:20373851 | CAGAGTCATATTGAG[A/C/T]AGGACATGGGAAACA | 7011 |
rs769631716 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393141 | AGAATGGTGTGAACC[C/T]AGGAGGTGGAGCTTG | 7011 |
rs769649189 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408104 | ACTAGAGAGGGTGGC[C/T]AGGCACCGGTTCTCC | 7011 |
rs769670309 | snp | C/T | 1.81437e-05 | 0.0030119 | intron-variant | TEP1 | GRCh38.p7 | 14:20383363 | TACACACTGTGATAT[C/T]TGGGCAAAGGGGCAG | 7011 |
rs769720913 | snp | C/G | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377684 | TGAGTGCCACAGAGA[C/G]GGCAGGAGAGAGAGA | 7011 |
rs769721921 | snp | A/G | 1.65108e-05 | 0.00287317 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389688 | TAAAGCTGTTTGGCC[A/G]CATTTATCATTCCAT | 7011 |
rs769724263 | snp | C/T | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383500 | CACCCGGGGAAGCTT[C/T]TTTGGGATCCAGTCT | 7011 |
rs769750298 | in-del | -/A | 5.05642e-05 | 0.00502788 | intron-variant | TEP1 | GRCh38.p7 | 14:20368778 | CGCACACACACACAC[-/A]CACACACACACACAC | 7011 |
rs769762249 | snp | C/T | 0.000942477 | 0.0216876 | intron-variant | TEP1 | GRCh38.p7 | 14:20396781 | TGAGAAGGCCAGGCA[C/T]AGTGGCATGCACCTA | 7011 |
rs769769958 | snp | A/G | 4.96208e-05 | 0.00498076 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395586 | TTTCATTTCTAGTTA[A/G]TATCCGCCTCATCAG | 7011 |
rs769849116 | snp | C/T | 6.58903e-05 | 0.00573941 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372760 | GGTGCCGAACCCTTC[C/T]GCAGTTTCACTTGCC | 7011 |
rs769887404 | snp | A/C | 1.74891e-05 | 0.00295707 | intron-variant | TEP1 | GRCh38.p7 | 14:20381086 | AGGGATATGAAGGGG[A/C]TGGTGAGAAGGGACA | 7011 |
rs769928020 | snp | C/G | 1.65252e-05 | 0.00287443 | intron-variant | TEP1 | GRCh38.p7 | 14:20401446 | TGCATGCTCAGGGTG[C/G]AGCTTCTCACCTGTA | 7011 |
rs769935556 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant | TEP1 | GRCh38.p7 | 14:20382591 | GAGAATGGGAAGTAG[C/T]GATTAGGACTTGGAA | 7011 |
rs769940204 | snp | C/T | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378833 | GTGATTTGGTACTGG[C/T]GAGCCTTAGTCTGCA | 7011 |
rs770021599 | snp | A/G | 1.76586e-05 | 0.00297136 | intron-variant | TEP1 | GRCh38.p7 | 14:20401163 | ATAGGTAAGAAAGAG[A/G]TCTATCATTTCAGAG | 7011 |
rs770044035 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369726 | CCTACTAGGATTCTC[C/T]AAGTTTATATCAAAG | 7011 |
rs770087888 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371534 | ATGCAAAGTAACTTC[A/C]AATCTGCTTTGGCCA | 7011 |
rs770094773 | snp | A/T | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414789 | TTCGTAAAGAATGTA[A/T]CTTACCCCCACGCAC | 7011 |
rs770095160 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | TEP1 | GRCh38.p7 | 14:20373263 | TCTCTCTCCAAGCCT[C/T]ACTCACCTGCTTCCT | 7011 |
rs770102977 | snp | C/T | 0.000164736 | 0.0090742 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384486 | GCCGGCCAGCTGCCA[C/T]ACCCCCCCACTCACA | 7011 |
rs770105422 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20386377 | TTGCAGCCCCAACCA[C/T]GCCCACCTCAGGTCC | 7011 |
rs770107747 | snp | A/C | 1.65083e-05 | 0.00287296 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20405450 | CTTCACACCTCAATA[A/C]CTTGAGGATAAACTC | 7011 |
rs770139350 | snp | A/G | 1.69352e-05 | 0.00290987 | intron-variant | TEP1 | GRCh38.p7 | 14:20380214 | TGGTGGGCTTACTAG[A/G]GTCTGGGGTCAAGGT | 7011 |
rs770141932 | in-del | -/G | 1.64925e-05 | 0.00287158 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378463 | CCTGCCCCTCTGGGT[-/G]GAAGGCAACACAGTT | 7011 |
rs770172232 | snp | C/T | 3.29696e-05 | 0.00406001 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403742 | GAGCGGGGTGGCCGG[C/T]GGGGGTGTCTCTTGG | 7011 |
rs770176730 | snp | A/C/G/T | 4.98977e-05 | 0.0049947 | intron-variant | TEP1 | GRCh38.p7 | 14:20381908 | CTCTGCTGGGGCACC[A/C/G/T]GTACCTGCGCAGACT | 7011 |
rs770182518 | snp | C/T | 0.000103708 | 0.00720021 | intron-variant | TEP1 | GRCh38.p7 | 14:20368759 | GGATAGGTGTGCAGG[C/T]GCACGCACACACACA | 7011 |
rs770199026 | snp | A/G | 2.02879e-05 | 0.00318489 | intron-variant | TEP1 | GRCh38.p7 | 14:20383731 | AGGCTGGGCTCATTG[A/G]GGGATACCCACCGGT | 7011 |
rs770200088 | snp | C/T | 1.64966e-05 | 0.00287194 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373714 | CTGCACAGTGGCTAA[C/T]GGGTCCTGAGTGAGC | 7011 |
rs770223909 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405887 | GGCATGGCAGTGCAC[A/G]CCTGTAATTCCAGCT | 7011 |
rs770232558 | snp | C/T | 1.65252e-05 | 0.00287443 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389291 | ATTGGGATTCAAATC[C/T]GTTGACCTGGCAAAG | 7011 |
rs770239403 | in-del | -/CTC | 0.000398592 | 0.0141116 | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373805 | CACAGACACCACGTG[-/CTC]CTCCTGCCCACAGAG | 7011 |
rs770277833 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395908 | GGCATCATGGGCGTT[A/G]AGAAATCTGAATGGA | 7011 |
rs770287420 | snp | A/G | 1.65075e-05 | 0.00287289 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385106 | CTGAAGGGTACTGCT[A/G]GGCCTGCGGGGAGGA | 7011 |
rs770290403 | in-del | -/AT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368779 | CACACACACACACAC[-/AT]ACACACACACACACT | 7011 |
rs770292837 | snp | C/G/T | 3.2948e-05 | 0.00405871 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401019 | GACGCTTTGTTCCCC[C/G/T]GTAGGCTCAGCTCCC | 7011 |
rs770312455 | snp | A/G | 1.67315e-05 | 0.00289231 | intron-variant | TEP1 | GRCh38.p7 | 14:20395992 | GAGCACAGGAGCCGG[A/G]AGTATGGGGGGCTTC | 7011 |
rs770320555 | snp | A/G | 1.67773e-05 | 0.00289626 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371626 | TAGAATTCGGTTCAG[A/G]TGAAGACTAGCTCAA | 7011 |
rs770384184 | snp | C/T | 8.25348e-05 | 0.00642344 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384158 | AGGACTCGGTGGCTT[C/T]TGCAGCTGCTGGAAG | 7011 |
rs770400588 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394211 | CCTCCCAAGTAGGTG[C/G]GACTACAAGTGCAAG | 7011 |
rs770420127 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391653 | AGCATCTGTCAGATA[A/G]ACCAAGACAGTGCGG | 7011 |
rs770428466 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408373 | AGTCAGGGAGCATAG[C/T]CAGGCACCGGTTCTC | 7011 |
rs770439241 | snp | C/T | 5.02719e-05 | 0.00501332 | intron-variant | TEP1 | GRCh38.p7 | 14:20384267 | TGACTATCCATGGTG[C/T]CATGCTCCTCAGCAC | 7011 |
rs770441743 | snp | A/G | 1.64961e-05 | 0.00287189 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377368 | GAGGGACTGAAGGGA[A/G]CATTCCTTGAGTGCC | 7011 |
rs770458851 | snp | A/C | 1.65051e-05 | 0.00287267 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378475 | GGTGGAAGGCAACAC[A/C]GTTCAGGGACTTGGG | 7011 |
rs770468262 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406287 | AGATTCAGAGTCTCC[A/G]GAGGTGAGCTTCACG | 7011 |
rs770488810 | snp | G/T | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391722 | CACAGCTGTCTCTAG[G/T]GCCTGTCGGTACCTG | 7011 |
rs770502366 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369464 | TGGAGTTTGGGTTTC[C/T]GGAGTGTTTGCTTTT | 7011 |
rs770514028 | snp | A/T | 2.05392e-05 | 0.00320455 | intron-variant | TEP1 | GRCh38.p7 | 14:20377244 | AGAAAAGAAAAGAAC[A/T]GTAATTTGTTAACCC | 7011 |
rs770515478 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369561 | CCATCAGAGCTGGCA[C/T]ACAAAAATGAGGACT | 7011 |
rs770542657 | in-del | -/TCACTATCCATGCTGGCA | 0.000329459 | 0.0128305 | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369381 | AGATGTGGTGTTGGC[-/TCACTATCCATGCTGGCA]TCACTATCCATGCTG | 7011 |
rs770549335 | snp | C/T | 3.29962e-05 | 0.00406165 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380942 | TCACCATAGAGGGCA[C/T]GGGCCTCCAAGAGCC | 7011 |
rs770560423 | snp | C/T | 6.6454e-05 | 0.0057639 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381676 | GCTCCAGAGGGCCCT[C/T]CCCTAGCAAACTGTC | 7011 |
rs770562671 | snp | C/T | 1.65315e-05 | 0.00287498 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368416 | GCACAAGGGGTATCA[C/T]TATTCCCGAGTGGCA | 7011 |
rs770570913 | snp | C/G | 3.30759e-05 | 0.00406655 | intron-variant | TEP1 | GRCh38.p7 | 14:20390645 | GCAGAGGAAAATGTG[C/G]GGGAGGGAGAGGGTT | 7011 |
rs770605183 | snp | C/G | 5.27125e-05 | 0.00513356 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383638 | CTGCAGCTCCCACAC[C/G]AGGCTTCTGTACATG | 7011 |
rs770615507 | snp | A/G | | | | | GRCh38.p7 | 14:20415586 | ATACAAAAATTAGCC[A/G]GGCATGGTGGTGGCC | 7011 |
rs770633564 | snp | C/T | 1.69384e-05 | 0.00291014 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383209 | CCTCCAGCCGCTTCC[C/T]GTACAGGGCCAGCTC | 7011 |
rs770684074 | in-del | -/TTTGTGGTTTTTT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410796 | GCTAATTGTTTCTCC[-/TTTGTGGTTTTTT]TTTTTTTTTTTTTTT | 7011 |
rs770707233 | snp | A/G | 1.64939e-05 | 0.0028717 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377697 | GAGGGCAGGAGAGAG[A/G]GAAAGGGAACCCAGG | 7011 |
rs770713478 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20404013 | AGCCCTAGCTCCAAA[A/G]TCACAATTTCTGTGG | 7011 |
rs770745299 | snp | A/C | 1.65825e-05 | 0.00287941 | intron-variant | TEP1 | GRCh38.p7 | 14:20388078 | CCTGACATAAATAAC[A/C]AGATAAATGAGAGTA | 7011 |
rs770758335 | snp | A/C | 1.7949e-05 | 0.00299569 | intron-variant | TEP1 | GRCh38.p7 | 14:20377791 | AAGGATACCACCTCC[A/C]CCACGCGGTCCTCCT | 7011 |
rs770780604 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408121 | GGCACCGGTTCTCCA[A/G]GGAGAGGATGTCTGG | 7011 |
rs770809212 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393090 | GGCGTGGTGGTGGGT[G/T]CCTGCAGTCCCAGCT | 7011 |
rs770815834 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372862 | TGGCCTGGAGCCTGG[C/T]GTACACAACAAGTTC | 7011 |
rs770822923 | snp | A/T | 3.31356e-05 | 0.00407022 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382058 | GCAGCTGGTCCACAG[A/T]CAAACCTGAAAACTC | 7011 |
rs770829386 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372647 | CAATTGACCTAGTTC[A/T]GAAGCAGAAGTGCAG | 7011 |
rs770841332 | in-del | -/G | 1.91364e-05 | 0.00309319 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386606 | TGGATGAAATGAAAA[-/G]GCCGGATGCTGCGCC | 7011 |
rs770887029 | snp | A/G | 0.000214896 | 0.0103635 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404693 | AGGTGGGGGCGACAC[A/G]CCGGCAAGAAAGCAG | 7011 |
rs770889621 | snp | A/T | 1.64955e-05 | 0.00287184 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381398 | CATGTCTTCCAGAGC[A/T]GAGCTGCATGAACAG | 7011 |
rs770890566 | in-del | -/C | 1.84463e-05 | 0.00303691 | intron-variant | TEP1 | GRCh38.p7 | 14:20396606 | CCCCATGGCTACCAG[-/C]CCCCTCACACATACC | 7011 |
rs770948068 | snp | G/T | 1.65384e-05 | 0.00287557 | intron-variant | TEP1 | GRCh38.p7 | 14:20386661 | GCTCAGTCTAGGGAT[G/T]ATTCCCACCCCCCAT | 7011 |
rs770949541 | snp | C/T | 6.97569e-05 | 0.00590539 | intron-variant | TEP1 | GRCh38.p7 | 14:20386408 | ACCACTCAAGCCCCT[C/T]ATCCCCGACCCAGCC | 7011 |
rs770979131 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376876 | GTGTATTTTCATACA[C/T]ATATACATACAACTT | 7011 |
rs771040504 | in-del | -/TGAT | 1.64814e-05 | 0.00287061 | intron-variant | TEP1 | GRCh38.p7 | 14:20378893 | CTCTGGACCCTGGCC[-/TGAT]ATCAGCTCCCTCCTC | 7011 |
rs771045165 | snp | C/T | 8.23839e-05 | 0.00641757 | intron-variant | TEP1 | GRCh38.p7 | 14:20384585 | TACAGGTGCTCCCTA[C/T]CTCCCTCAGCTCACC | 7011 |
rs771045455 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406864 | GGAGTGTTATATGTA[C/T]GTATGACTCTTTGCA | 7011 |
rs771079264 | snp | C/G | 3.30508e-05 | 0.00406501 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379078 | AAGCAGAGATTCCAT[C/G]ACAGCCACTCACCAC | 7011 |
rs771100825 | snp | A/G | 1.65362e-05 | 0.00287538 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405562 | TGAGACCAGAGTAGA[A/G]CACAGCAAGCTCAGT | 7011 |
rs771115273 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382684 | AGGTAGAGCGGCCGG[C/T]CTGATTCCCGCTTCA | 7011 |
rs771118554 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384657 | AGTTCTGAGATCCGA[C/T]GTGCGGCCTCTTCAG | 7011 |
rs771195290 | snp | A/C | 1.65021e-05 | 0.00287241 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20401456 | GGGTGCAGCTTCTCA[A/C]CTGTAACCCAGCAGG | 7011 |
rs771239348 | snp | G/T | 6.59544e-05 | 0.0057422 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383523 | TCCAGTCTGAAATCA[G/T]CTGCCCATTCTGGTC | 7011 |
rs771264352 | snp | C/T | 8.23621e-05 | 0.00641672 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372750 | CAAATTTCCGGGTGC[C/T]GAACCCTTCCGCAGT | 7011 |
rs771270391 | snp | A/G | 1.68653e-05 | 0.00290385 | intron-variant | TEP1 | GRCh38.p7 | 14:20396000 | GAGCCGGGAGTATGG[A/G]GGGCTTCAGGGGTCC | 7011 |
rs771303551 | snp | A/T | 1.65756e-05 | 0.00287881 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395597 | GTTAGTATCCGCCTC[A/T]TCAGTGTTATATTCG | 7011 |
rs771313416 | snp | G/T | 3.2969e-05 | 0.00405998 | intron-variant | TEP1 | GRCh38.p7 | 14:20371178 | AAAACACTGGTCCTA[G/T]ACGAATGTTTGCTTT | 7011 |
rs771339460 | snp | A/G | 1.7402e-05 | 0.0029497 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396632 | ATACCGCATGCTGGA[A/G]TCTCTGGAGAATGAG | 7011 |
rs771341751 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388720 | GCTCAGGCAGACATA[C/T]TGAATTATGAGGTAG | 7011 |
rs771349197 | snp | A/C | 8.24518e-05 | 0.00642021 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405461 | AATACCTTGAGGATA[A/C]ACTCAGGCTCCAGGA | 7011 |
rs771364011 | snp | C/T | 1.64961e-05 | 0.00287189 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378181 | CCCACAGCCACAACC[C/T]CCCCAGGCACATTGA | 7011 |
rs771410997 | snp | A/C/G | 0.000131783 | 0.00811646 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382636 | ACCTGCTCATACAGC[A/C/G]TGAAGAGCCTCAGGT | 7011 |
rs771416986 | snp | A/T | 1.72904e-05 | 0.00294022 | intron-variant | TEP1 | GRCh38.p7 | 14:20395415 | CAGGGTAGCCCCGAT[A/T]GCCCACCCTTGGCTC | 7011 |
rs771448949 | in-del | -/C | 1.85924e-05 | 0.00304891 | intron-variant | TEP1 | GRCh38.p7 | 14:20383137 | TAGCTCCCAGATTCA[-/C]CCCCACACACCCACC | 7011 |
rs771457052 | snp | A/C | 3.3712e-05 | 0.00410547 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368863 | CTGTCACCAGCAACT[A/C]AGGTAGCACATGGAG | 7011 |
rs771496676 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393074 | ACAAAAAAATTAGCC[A/G]GGCGTGGTGGTGGGT | 7011 |
rs771508631 | snp | A/T | 1.79796e-05 | 0.00299825 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383305 | GGCTCTGCTCAAGGG[A/T]CTCCCCTAGGCCTGC | 7011 |
rs771543900 | in-del | -/T | 9.90508e-05 | 0.00703673 | intron-variant | TEP1 | GRCh38.p7 | 14:20373221 | AGGCCACCCTTGACC[-/T]TTTTTTTGTGCCAGT | 7011 |
rs771553761 | snp | C/T | 3.33778e-05 | 0.00408507 | splice-acceptor-variant | TEP1 | GRCh38.p7 | 14:20380054 | AGAGACAGGCTGGAG[C/T]TAGAGAAAGAGTAGG | 7011 |
rs771562979 | snp | C/T | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373273 | AGCCTCACTCACCTG[C/T]TTCCTTAGGAACCTG | 7011 |
rs771582939 | snp | C/T | 0.000118515 | 0.00769696 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383238 | TCCTCTCTCACCAGC[C/T]GGGCCCGAGCAGAGG | 7011 |
rs771603201 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397265 | TATATACTAACATAA[G/T]GTAGCACATTCATTA | 7011 |
rs771607548 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20391315 | AAGTTCAACACCGGG[A/G]TGTAGTGAGGTGAAA | 7011 |
rs771613327 | snp | A/T | 1.69769e-05 | 0.00291345 | intron-variant | TEP1 | GRCh38.p7 | 14:20371640 | GGTGAAGACTAGCTC[A/T]AAAAAGTACATGGAC | 7011 |
rs771619009 | snp | A/C | 6.6096e-05 | 0.00574836 | intron-variant | TEP1 | GRCh38.p7 | 14:20389311 | ACCTGGCAAAGGAAG[A/C]AGCAGTCATTAACCA | 7011 |
rs771643432 | snp | C/T | 1.64985e-05 | 0.0028721 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381963 | CATGGGGTAGGGGTC[C/T]CCACTGTTACCAGCA | 7011 |
rs771645662 | in-del | -/CTT | 1.64727e-05 | 0.00286986 | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369511 | CTGTGGTCCATTCTC[-/CTT]CTGGGCTGCATTTGG | 7011 |
rs771672252 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408737 | CTTTGGGAGCTGAGG[A/C]AAGAGGATTCCTTGA | 7011 |
rs771699947 | snp | C/G | 3.29783e-05 | 0.00406055 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377386 | TTCCTTGAGTGCCCA[C/G]CCCTGCAAGGACCCA | 7011 |
rs771702112 | snp | A/G | 1.64906e-05 | 0.00287142 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378807 | GGCAGTCTGGGCTCA[A/G]GCAGCAGCCAGTGAT | 7011 |
rs771704995 | in-del | -/AC | 1.64732e-05 | 0.0028699 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408234 | TGTCTGGGTGGGCAG[-/AC]ACACATATCCATGTG | 7011 |
rs771717141 | snp | C/T | 1.73333e-05 | 0.00294386 | intron-variant | TEP1 | GRCh38.p7 | 14:20386431 | ACCCAGCCCCTCTTC[C/T]CTGCAGCCCCCACAC | 7011 |
rs771747875 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408550 | CCCCACAGCCCTCCT[A/G]ATAATGCCAATGATT | 7011 |
rs771754937 | snp | C/T | 1.65075e-05 | 0.00287289 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377482 | TGCCTGACCCTGAGC[C/T]CCCTGGGAACCTAGA | 7011 |
rs771764886 | snp | C/G | 1.67237e-05 | 0.00289164 | intron-variant | TEP1 | GRCh38.p7 | 14:20373828 | GCCCACAGAGCACAA[C/G]ATCAGAGCAGAGTCA | 7011 |
rs771770564 | snp | G/T | 1.65151e-05 | 0.00287355 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384182 | CTGGAAGGTGGCCTG[G/T]ACCAAGTCATCGTCT | 7011 |
rs771775602 | snp | A/G | 1.65861e-05 | 0.00287972 | intron-variant | TEP1 | GRCh38.p7 | 14:20406403 | CAAACCAACGACCCT[A/G]GGGTAGTAGTGGCAG | 7011 |
rs771787577 | snp | A/G | 3.29516e-05 | 0.00405891 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403746 | GGGGTGGCCGGCGGG[A/G]GTGTCTCTTGGCCCG | 7011 |
rs771792941 | snp | C/T | 4.94711e-05 | 0.00497324 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380957 | TGGGCCTCCAAGAGC[C/T]GAGAGACCAGACCCA | 7011 |
rs771807692 | snp | A/C | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389651 | ACCAACAAAGAGGCA[A/C]TTGGAATTCACACGC | 7011 |
rs771831047 | snp | G/T | 3.5256e-05 | 0.00419842 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407877 | GGAGCTATTACCAAA[G/T]TTGCTTCCTGAGCTG | 7011 |
rs771853755 | snp | C/T | 3.59247e-05 | 0.00423805 | intron-variant | TEP1 | GRCh38.p7 | 14:20375704 | GTGGGGAGTGTTGTC[C/T]TGCCCCAGGAACCCA | 7011 |
rs771907123 | snp | C/T | 0.000100293 | 0.00708069 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375829 | AGGAGTGGATCAAAA[C/T]AGGGGTTTTGGGTGT | 7011 |
rs771915301 | snp | C/G | 1.65326e-05 | 0.00287507 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404698 | GGGGCGACACGCCGG[C/G]AAGAAAGCAGCAATG | 7011 |
rs771941999 | snp | G/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369500 | CCACATGTTACCTGT[G/T]GTCCATTCTCCTTCT | 7011 |
rs771945224 | snp | G/T | 1.6486e-05 | 0.00287102 | intron-variant | TEP1 | GRCh38.p7 | 14:20390930 | ATGGTGGGTGTTGAG[G/T]GTCTGACCTGGACTT | 7011 |
rs771961812 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20384327 | CAAGCTACTTCCTCC[C/G]CAGGACAACCCAGAC | 7011 |
rs771966236 | snp | A/G | 3.29468e-05 | 0.00405861 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401028 | TTCCCCCGTAGGCTC[A/G]GCTCCCGCTCCCAGG | 7011 |
rs771970154 | snp | A/G | 3.60036e-05 | 0.0042427 | intron-variant | TEP1 | GRCh38.p7 | 14:20404798 | GGGTGAGAGGACTAG[A/G]ATCTCAGTCACTCCT | 7011 |
rs771998185 | snp | C/G | 1.67393e-05 | 0.00289299 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386487 | TGACGCCCCAGCGGA[C/G]GTCGATTCCGTGAAG | 7011 |
rs772028695 | snp | C/T | 1.64874e-05 | 0.00287113 | intron-variant | TEP1 | GRCh38.p7 | 14:20369580 | AAAATGAGGACTCTG[C/T]CATTTTAAGGACAGA | 7011 |
rs772030168 | snp | C/G | 1.6531e-05 | 0.00287493 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379083 | GAGATTCCATCACAG[C/G]CACTCACCACAGACT | 7011 |
rs772035464 | snp | A/T | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373122 | AGCAGTGACGGCTGC[A/T]GAACTCCTTGGTATA | 7011 |
rs772076088 | snp | C/T | 1.65452e-05 | 0.00287616 | intron-variant | TEP1 | GRCh38.p7 | 14:20378712 | CACGAGGGTGAGTCA[C/T]GGCTCAGGGCCACTC | 7011 |
rs772079805 | in-del | -/TGTTCC | 1.64743e-05 | 0.00287 | cds-indel, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401010 | CCCAGACCGACGCTT[-/TGTTCC]TGTTCCCCCGTAGGC | 7011 |
rs772081432 | snp | C/T | 9.93888e-05 | 0.00704872 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377719 | GAACCCAGGTGCCCA[C/T]GGGGCCGACCCAGAG | 7011 |
rs772100908 | snp | C/T | 3.29815e-05 | 0.00406075 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384667 | TCCGACGTGCGGCCT[C/T]TTCAGACTCAGAAAC | 7011 |
rs772108521 | snp | C/T | 1.67565e-05 | 0.00289447 | intron-variant | TEP1 | GRCh38.p7 | 14:20384282 | CCATGCTCCTCAGCA[C/T]TCCCAGGCTAAAACT | 7011 |
rs772109268 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388533 | GACAGATAAAAAAAA[C/T]GTGAAAAGATTTCTG | 7011 |
rs772156404 | snp | A/G | 1.77329e-05 | 0.0029776 | intron-variant | TEP1 | GRCh38.p7 | 14:20383651 | ACCAGGCTTCTGTAC[A/G]TGGAGAGGAAGTCAG | 7011 |
rs772191389 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408227 | GGAGAGGATGTCTGG[G/T]TGGGCAGACACATAT | 7011 |
rs772217222 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371291 | TGGGTGGACAATATC[A/G]TAGGATTTTCTGTAT | 7011 |
rs772264373 | snp | A/G | 3.30038e-05 | 0.00406212 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381649 | CAGGGAGGCACAGCC[A/G]GGCACCAGGGCGCTC | 7011 |
rs772284515 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405048 | CCTCCTGCATCAACA[A/G]CTATCAAAAATTTAT | 7011 |
rs772286946 | snp | C/G | 3.3335e-05 | 0.00408245 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404632 | AAGCTCAGCCACCTG[C/G]ATCCAGTCAGAAGGC | 7011 |
rs772290105 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408130 | TCTCCAAGGAGAGGA[C/T]GTCTGGGTGGGCAGA | 7011 |
rs772334262 | in-del | -/CACT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20371200 | GTTTGCTTTAGCACA[-/CACT]CAAATAGGACTTACC | 7011 |
rs772348402 | snp | A/G | 2.04664e-05 | 0.00319887 | intron-variant | TEP1 | GRCh38.p7 | 14:20383706 | CAGGGGTGGTACGTG[A/G]GCATCAACAAGGCTG | 7011 |
rs772406940 | snp | C/T | 1.65362e-05 | 0.00287538 | intron-variant | TEP1 | GRCh38.p7 | 14:20382195 | ACCCTGGCCCTCAGC[C/T]TCCCAACCAACCCAC | 7011 |
rs772412060 | snp | A/T | 3.65651e-05 | 0.00427565 | intron-variant | TEP1 | GRCh38.p7 | 14:20376312 | CTGAAAGAGGAAGCC[A/T]GACAGGCCCTGGGAG | 7011 |
rs772413075 | snp | G/T | 6.84779e-05 | 0.00585101 | intron-variant | TEP1 | GRCh38.p7 | 14:20369297 | ATAGGTGTGAGCCAC[G/T]GCTCCCAGCCCTCCC | 7011 |
rs772425594 | in-del | -/GAAGA | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402398 | ATATATTAATAGGAT[-/GAAGA]GAAAAGACGAGTTGA | 7011 |
rs772438520 | snp | A/G | 1.69798e-05 | 0.00291369 | intron-variant | TEP1 | GRCh38.p7 | 14:20405607 | ATTGAGAAAGAGGGA[A/G]GAAATGAGAAGAGAG | 7011 |
rs772442681 | snp | A/G | 1.64999e-05 | 0.00287222 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391622 | GGTTGCTCTTTGGAC[A/G]GAGCCTGTCTGCATT | 7011 |
rs772450686 | snp | A/C | 1.64814e-05 | 0.00287061 | intron-variant | TEP1 | GRCh38.p7 | 14:20373496 | TGACTCTGGTCCTTG[A/C]AGGAACTCACCAAGA | 7011 |
rs772453193 | snp | A/C | 1.6473e-05 | 0.00286988 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20371488 | GCATTTTGGATCTTA[A/C]CAGATTTCAGATGGA | 7011 |
rs772455005 | snp | C/T | 1.65138e-05 | 0.00287343 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368427 | ATCATTATTCCCGAG[C/T]GGCACATCTTCATTC | 7011 |
rs772469823 | snp | A/C | 1.64895e-05 | 0.00287132 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378452 | TGTGGCTATTACCTG[A/C]CCCTCTGGGTGGAAG | 7011 |
rs772482004 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409606 | CCTTCCTTTGCCCCC[G/T]TTGCCCACTGGAGTT | 7011 |
rs772488924 | snp | C/G | 1.6522e-05 | 0.00287414 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401576 | TGTATCACCGGCCTT[C/G]TCAAACTGTGGAAAC | 7011 |
rs772497739 | snp | C/T | 9.798e-05 | 0.0069986 | intron-variant | TEP1 | GRCh38.p7 | 14:20396748 | GTGGAATGTGGGGCA[C/T]AGAGTGAGAAAAACA | 7011 |
rs772505484 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387945 | GGCTTGGAGTGTCCT[C/T]TTCCAGTGGCCGGAG | 7011 |
rs772546728 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367114 | CACGCCTGTAATCCC[A/C]GAACTTTAAGAGGCT | 7011 |
rs772548432 | snp | C/T | 1.65053e-05 | 0.0028727 | intron-variant | TEP1 | GRCh38.p7 | 14:20378338 | CACCCTCCACTCCTG[C/T]CCTCCTGTGCTTCCC | 7011 |
rs772680203 | snp | A/G | 3.29533e-05 | 0.00405901 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373384 | CGCTGTGTCCCAGGA[A/G]GGTGTGGGTTTGGCA | 7011 |
rs772715346 | snp | A/G | 1.67374e-05 | 0.00289282 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376252 | CTTGGCCACAGCTGC[A/G]CTGTGAAATCCTCTG | 7011 |
rs772733255 | snp | C/T | 1.66485e-05 | 0.00288513 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380450 | AGCCTCGGGGAGCTT[C/T]TGTTCCTCTTTGGGG | 7011 |
rs772749184 | snp | A/G | | | | | GRCh38.p7 | 14:20415996 | GGTCTGTTTAGAGGA[A/G]AAAGAGAGGAGTTTG | 7011 |
rs772763908 | snp | C/G | 1.66322e-05 | 0.00288371 | intron-variant | TEP1 | GRCh38.p7 | 14:20403932 | AAGACCCAAACCAAC[C/G]CTCCAAAACAAAACG | 7011 |
rs772769095 | snp | C/T | 1.85451e-05 | 0.00304503 | intron-variant | TEP1 | GRCh38.p7 | 14:20383140 | GCTCCCAGATTCACC[C/T]CACACACCCACCGGC | 7011 |
rs772799601 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409671 | TACCTTGGGATCTTG[C/G]TTGGATAAGATACTT | 7011 |
rs772800825 | snp | C/T | 0.000131787 | 0.00811641 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380294 | TGTGTGTTGGAGGTG[C/T]CATCTCCGGGAGAGC | 7011 |
rs772818538 | snp | C/G | 1.66059e-05 | 0.00288144 | intron-variant | TEP1 | GRCh38.p7 | 14:20369328 | CTAGTATTTCTGACC[C/G]TTCCTTCAAACTCAC | 7011 |
rs772871734 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant | TEP1 | GRCh38.p7 | 14:20372860 | TGTGGCCTGGAGCCT[A/G]GTGTACACAACAAGT | 7011 |
rs772873649 | snp | C/T | 1.88443e-05 | 0.00306949 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368893 | GGGCTGTGACAGAGC[C/T]CGAGTGAATCTCAAA | 7011 |
rs772873737 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366330 | TGCAATTGGCCCAAG[A/C]TTTTAGGGGAGCAAA | 7011 |
rs772892463 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408758 | GATTCCTTGAGCCCA[A/G]GAGTTTGAGGCAAGC | 7011 |
rs772896832 | snp | C/T | 1.64931e-05 | 0.00287163 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382704 | TTCCCGCTTCACCAG[C/T]AGCAGTCGCATCTGG | 7011 |
rs772907686 | snp | A/G | 0.00211004 | 0.0324124 | intron-variant | TEP1 | GRCh38.p7 | 14:20377235 | AAAAAAAAAAGAAAA[A/G]AAAAGAACAGTAATT | 7011 |
rs772928207 | in-del | -/TGG | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402170 | AAAATTAGCTGGGCA[-/TGG]TGGTGGATGTCTGTA | 7011 |
rs772941023 | snp | A/C | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414555 | CACGATATGAGGATA[A/C]AAGAAAACAGCCATC | 7011 |
rs772956301 | snp | A/G | 0.000115322 | 0.00759261 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403836 | TCATGGCAGTACGGA[A/G]ACAGGCGGGCAGGGG | 7011 |
rs773002131 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20371147 | CCCTATCCTCCATGA[C/T]GGGCCCCAAGGTGTA | 7011 |
rs773015509 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387961 | TTCCAGTGGCCGGAG[A/G]GACTGGACCCCTGTC | 7011 |
rs773020627 | snp | A/T | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377628 | GTAGATCCTAATGCC[A/T]TCCGCTCGATATCCA | 7011 |
rs773043868 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367145 | GAGGTGTGCAGATAA[A/C]CTGAGGTCAGGAGTT | 7011 |
rs773072424 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383511 | GCTTCTTTGGGATCC[A/G]GTCTGAAATCAGCTG | 7011 |
rs773076670 | snp | C/T | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381998 | CTGCTTCTTCCCAGC[C/T]CTTAGTCCCCTTCGG | 7011 |
rs773077493 | snp | A/C | 3.29821e-05 | 0.00406078 | intron-variant | TEP1 | GRCh38.p7 | 14:20371167 | CCCAAGGTGTAAAAA[A/C]ACTGGTCCTAGACGA | 7011 |
rs773081287 | snp | G/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391639 | AGCCTGTCTGCATTA[G/T]CATCTGTCAGATAGA | 7011 |
rs773089429 | snp | A/C | 0.000576616 | 0.0169698 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374476 | GACCCAGGAACTGAC[A/C]AAGCCGCTGTCCTGA | 7011 |
rs773090561 | snp | A/G/T | 9.88915e-05 | 0.00703114 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386086 | TTACCCAGTGGAAGT[A/G/T]TGGATGGTCAGGAAG | 7011 |
rs773096736 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368780 | CACACACACACACAC[-/A]CACACACACACACTT | 7011 |
rs773104274 | snp | A/G | 1.65124e-05 | 0.00287331 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389690 | AAGCTGTTTGGCCAC[A/G]TTTATCATTCCATCA | 7011 |
rs773145627 | snp | A/G | 1.99416e-05 | 0.00315759 | intron-variant | TEP1 | GRCh38.p7 | 14:20383932 | GCCTGCATGGGACAG[A/G]AACAGAAAACATGGT | 7011 |
rs773177980 | snp | A/C/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390697 | GGAACCCTTTGGCCA[A/C/G]CCAGAGACAGCAGGT | 7011 |
rs773217634 | snp | A/G | 4.94173e-05 | 0.00497053 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372761 | GTGCCGAACCCTTCC[A/G]CAGTTTCACTTGCCA | 7011 |
rs773223189 | snp | A/G | 1.76331e-05 | 0.00296922 | intron-variant | TEP1 | GRCh38.p7 | 14:20381091 | TATGAAGGGGCTGGT[A/G]AGAAGGGACAGTTTA | 7011 |
rs773263429 | snp | A/G | 1.70411e-05 | 0.00291895 | intron-variant | TEP1 | GRCh38.p7 | 14:20395437 | CCTTGGCTCCCAGAC[A/G]GTGCATACATACCTG | 7011 |
rs773275695 | snp | A/C | 0.000395844 | 0.0140629 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384487 | CCGGCCAGCTGCCAC[A/C]CCCCCCCACTCACAG | 7011 |
rs773357648 | snp | A/G | 1.65203e-05 | 0.002874 | intron-variant | TEP1 | GRCh38.p7 | 14:20377531 | GAGTAAGACACTTGG[A/G]AAGGGGTAGGGGGCA | 7011 |
rs773387870 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405079 | TCTGGGTTCAAATCA[C/T]TGATTAAACCTGCCA | 7011 |
rs773396602 | snp | A/G | 1.65663e-05 | 0.002878 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380036 | GGGGATGAGGAAACT[A/G]CCAGAGACAGGCTGG | 7011 |
rs773397173 | snp | C/T | 1.64779e-05 | 0.00287031 | intron-variant | TEP1 | GRCh38.p7 | 14:20384359 | ACCCCATGTCCCTCT[C/T]CATGCCTCTGGTCAC | 7011 |
rs773404386 | snp | A/C | 1.64833e-05 | 0.00287078 | intron-variant | TEP1 | GRCh38.p7 | 14:20373267 | TCTCCAAGCCTCACT[A/C]ACCTGCTTCCTTAGG | 7011 |
rs773422112 | snp | A/G | 0.000115453 | 0.00759693 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381386 | GCATCAGCGTCACAT[A/G]TCTTCCAGAGCTGAG | 7011 |
rs773447583 | snp | G/T | 1.65685e-05 | 0.00287819 | intron-variant | TEP1 | GRCh38.p7 | 14:20403689 | CCTTCCTGGAGAAAA[G/T]GGGCGTGGGTCGAGG | 7011 |
rs773471753 | snp | C/T | 5.32931e-05 | 0.00516175 | intron-variant | TEP1 | GRCh38.p7 | 14:20401166 | GGTAAGAAAGAGGTC[C/T]ATCATTTCAGAGTCA | 7011 |
rs773473617 | snp | A/T | 1.64942e-05 | 0.00287173 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405458 | CTCAATACCTTGAGG[A/T]TAAACTCAGGCTCCA | 7011 |
rs773475088 | snp | C/T | 8.24599e-05 | 0.00642053 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378981 | GGGAGGACCCCTTAC[C/T]GACAACCATGCTGCA | 7011 |
rs773478455 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408267 | TTTTCCATGGTCTTC[A/G]GGTCAGGAAGCGTGG | 7011 |
rs773497924 | snp | C/T | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386578 | GTCCCGCTCCCCATG[C/T]ATGTCTCGGAAAGTG | 7011 |
rs773501350 | snp | G/T | 3.29538e-05 | 0.00405904 | intron-variant | TEP1 | GRCh38.p7 | 14:20384576 | ACATCTCTGTACAGG[G/T]GCTCCCTACCTCCCT | 7011 |
rs773512909 | snp | C/G | 2.02304e-05 | 0.00318038 | intron-variant | TEP1 | GRCh38.p7 | 14:20383733 | GCTGGGCTCATTGGG[C/G]GATACCCACCGGTAG | 7011 |
rs773536717 | snp | A/G | 8.45273e-05 | 0.0065005 | intron-variant | TEP1 | GRCh38.p7 | 14:20371635 | GTTCAGGTGAAGACT[A/G]GCTCAAAAAAGTACA | 7011 |
rs773538734 | snp | A/C/T | 9.89551e-05 | 0.0070334 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368546 | ACTGACCCTTCGCAT[A/C/T]GGAACAGGCCCAGCT | 7011 |
rs773545141 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394874 | TCTAGAAAGTTAAGT[G/T]AGTCCTGTGTTTGTT | 7011 |
rs773590007 | snp | A/G | 7.23314e-05 | 0.00601336 | intron-variant | TEP1 | GRCh38.p7 | 14:20383372 | TGATATTTGGGCAAA[A/G]GGGCAGGAAGGTAGA | 7011 |
rs773591904 | snp | C/T | 8.23649e-05 | 0.00641683 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371541 | GTAACTTCAAATCTG[C/T]TTTGGCCAAGATGAG | 7011 |
rs773651795 | in-del | -/TG | 1.66098e-05 | 0.00288177 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378524 | CAGCTGCCCACGGAC[-/TG]TGTCCCACAGCTGAG | 7011 |
rs773657080 | snp | A/G/T | 3.29485e-05 | 0.00405874 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391011 | ACTGCAGTCTTCAGA[A/G/T]TGTCACCTCCACACA | 7011 |
rs773671482 | snp | C/T | 1.67973e-05 | 0.00289799 | intron-variant | TEP1 | GRCh38.p7 | 14:20395997 | CAGGAGCCGGGAGTA[C/T]GGGGGGCTTCAGGGG | 7011 |
rs773692765 | snp | G/T | 1.95586e-05 | 0.00312712 | intron-variant | TEP1 | GRCh38.p7 | 14:20377252 | AAAGAACAGTAATTT[G/T]TTAACCCTGCCCACT | 7011 |
rs773705634 | in-del | -/A | 1.6674e-05 | 0.00288734 | intron-variant | TEP1 | GRCh38.p7 | 14:20373819 | GCTCCTCCTGCCCAC[-/A]GAGCACAAGATCAGA | 7011 |
rs773710293 | snp | A/C | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391049 | GTCCACCTGCTCCGC[A/C]CTCGTGATCATCATC | 7011 |
rs773714772 | snp | A/G | 1.6504e-05 | 0.00287258 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378082 | AGGAAAAGCGCAGCA[A/G]CAACAAAGCCATGGT | 7011 |
rs773723639 | snp | C/T | 0.000576469 | 0.0169677 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391655 | CATCTGTCAGATAGA[C/T]CAAGACAGTGCGGCC | 7011 |
rs773742611 | snp | A/G | 1.96593e-05 | 0.00313517 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383796 | GCCACGCAGATAGGT[A/G]CAGAGGCGTCTGAGC | 7011 |
rs773750181 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369488 | TGCTTTTTTCTGCCA[C/T]ATGTTACCTGTGGTC | 7011 |
rs773769593 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368760 | GATAGGTGTGCAGGC[A/G]CACGCACACACACAC | 7011 |
rs773778382 | snp | A/G | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385108 | GAAGGGTACTGCTGG[A/G]CCTGCGGGGAGGACA | 7011 |
rs773796816 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20373173 | AAGGACGTGTTTCAT[C/T]AGGAGCTGGGATACT | 7011 |
rs773826240 | snp | A/C | 0.00024899 | 0.0111549 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378169 | CTGTCCAGCCGGCCC[A/C]CAGCCACAACCCCCC | 7011 |
rs773872270 | snp | A/G | | | intron-variant, stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404673 | TGGCACAGAAATATC[A/G]TCGCAGGTGGGGGCG | 7011 |
rs773924414 | snp | C/T | 1.64931e-05 | 0.00287163 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377375 | TGAAGGGAGCATTCC[C/T]TGAGTGCCCAGCCCT | 7011 |
rs773932679 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406293 | AGAGTCTCCAGAGGT[A/G]AGCTTCACGGCCAGA | 7011 |
rs773939132 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368293 | CACATGAGAACACAG[G/T]CAGGCCTACACTTGA | 7011 |
rs773954864 | snp | G/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391723 | ACAGCTGTCTCTAGG[G/T]CCTGTCGGTACCTGT | 7011 |
rs773963019 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392593 | CAGTAGCTCAATGCC[A/G]TAAGAACAATTAAAA | 7011 |
rs773983990 | snp | A/C/G | 0.000321163 | 0.0126682 | stop-gained, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383210 | CTCCAGCCGCTTCCC[A/C/G]TACAGGGCCAGCTCC | 7011 |
rs774010179 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20407394 | GACACAGTCTCTCTC[G/T]GTTGCCCAGATTGGA | 7011 |
rs774020912 | snp | C/G | 6.59076e-05 | 0.00574016 | intron-variant | TEP1 | GRCh38.p7 | 14:20377594 | CACCCATTCCCATTT[C/G]AGTACCTGAAGAGAT | 7011 |
rs774044005 | snp | C/T | 1.67691e-05 | 0.00289556 | splice-acceptor-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381688 | CCTCCCCTAGCAAAC[C/T]GTCCTCGTGTGAGGA | 7011 |
rs774091569 | snp | A/G | 1.65567e-05 | 0.00287716 | intron-variant | TEP1 | GRCh38.p7 | 14:20400946 | GAGGCATAAATGGGG[A/G]AGAGAAGGAGGGAAT | 7011 |
rs774096923 | snp | A/G | 1.66882e-05 | 0.00288857 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379943 | ACCTGCCAAGTTCTC[A/G]GGTCCAACAGGTAAA | 7011 |
rs774098351 | snp | C/G/T | 8.56811e-05 | 0.00654481 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374485 | ACTGACCAAGCCGCT[C/G/T]TCCTGACTCTGGGTC | 7011 |
rs774113242 | in-del | -/ACACA | 0.000558986 | 0.0167087 | intron-variant | TEP1 | GRCh38.p7 | 14:20368782 | CACACACACACACAC[-/ACACA]CACACACTTACCAGC | 7011 |
rs774117599 | snp | A/G | 1.64787e-05 | 0.00287038 | intron-variant | TEP1 | GRCh38.p7 | 14:20373628 | AAGGGACGGAGCAGG[A/G]GAGAAAAGAAGAGAC | 7011 |
rs774123918 | snp | C/T | 1.74293e-05 | 0.00295201 | intron-variant | TEP1 | GRCh38.p7 | 14:20386414 | CAAGCCCCTCATCCC[C/T]GACCCAGCCCCTCTT | 7011 |
rs774136049 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20382517 | AGGCGAGGATAGGGA[G/T]TGGGTGATCACAAGA | 7011 |
rs774176858 | snp | A/G | 1.64776e-05 | 0.00287028 | intron-variant | TEP1 | GRCh38.p7 | 14:20372863 | GGCCTGGAGCCTGGT[A/G]TACACAACAAGTTCA | 7011 |
rs774186294 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20378731 | TCAGGGCCACTCTGA[A/C]CACTGCAGACCCCAA | 7011 |
rs774224758 | snp | A/C | 1.64806e-05 | 0.00287054 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20373010 | GGGTACACCGACTCA[A/C]CTGTGCTGTGGCCAC | 7011 |
rs774227713 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380377 | GGGGCAGGAGCCGGG[A/G]GTACTGGCTGAGGAT | 7011 |
rs774237207 | snp | G/T | 1.65562e-05 | 0.00287712 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384100 | GCCTTCCGTGGGGCA[G/T]CATCAGCCGTTGCAC | 7011 |
rs774266792 | in-del | -/GAAGG | 2.1285e-05 | 0.00326221 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396711 | CCGAAGCATGGCCAT[-/GAAGG]GAAGCTTCCCATTTT | 7011 |
rs774290424 | snp | A/G | 3.30147e-05 | 0.00406279 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384174 | TGCAGCTGCTGGAAG[A/G]TGGCCTGGACCAAGT | 7011 |
rs774324588 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374615 | TAGTGTAGGGTGGAA[C/G]GCGGTTAGCCACGTA | 7011 |
rs774363671 | in-del | -/TTAAATTC | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20365710 | GTCAGATATTACTTT[-/TTAAATTC]TTAAATTCCTACACA | 7011 |
rs774383904 | snp | C/G | 1.65408e-05 | 0.00287578 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389717 | ATCATCCATGCTTTG[C/G]CCAAGGAGGATGACC | 7011 |
rs774394312 | in-del | -/CCT | 1.64821e-05 | 0.00287067 | intron-variant | TEP1 | GRCh38.p7 | 14:20378902 | CCTGGCCATCAGCTC[-/CCT]CCTCATTTCCTTCTC | 7011 |
rs774408452 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20404249 | AATCCCAGCTACTTG[A/G]GAGGCTGAGGAAGGA | 7011 |
rs774410476 | snp | C/T | 1.65231e-05 | 0.00287424 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383541 | GCCCATTCTGGTCCA[C/T]TAACCTATCAGCCCC | 7011 |
rs774422044 | snp | A/G | 1.6795e-05 | 0.0028978 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380463 | TTTTGTTCCTCTTTG[A/G]GGACTGAAGAAGCTA | 7011 |
rs774436082 | snp | C/T | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378990 | CCTTACCGACAACCA[C/T]GCTGCAGGTCCCAGA | 7011 |
rs774463976 | snp | A/G | 1.65765e-05 | 0.00287888 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382060 | AGCTGGTCCACAGTC[A/G]AACCTGAAAACTCAA | 7011 |
rs774475423 | snp | A/G | 1.65143e-05 | 0.00287348 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378481 | AGGCAACACAGTTCA[A/G]GGACTTGGGGTAGGT | 7011 |
rs774477985 | snp | A/T | 1.64762e-05 | 0.00287016 | intron-variant | TEP1 | GRCh38.p7 | 14:20384591 | TGCTCCCTACCTCCC[A/T]CAGCTCACCTGCGGC | 7011 |
rs774490945 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393148 | TGTGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG | 7011 |
rs774497684 | in-del | -/TCACAATTTTC | 1.65321e-05 | 0.00287502 | intron-variant | TEP1 | GRCh38.p7 | 14:20386659 | GGCTCAGTCTAGGGA[-/TCACAATTTTC]TGATTCCCACCCCCC | 7011 |
rs774498126 | snp | G/T | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408027 | CGGTACAAATCAGCT[G/T]GCGTCATGTGAGATA | 7011 |
rs774558504 | snp | A/G | 1.67483e-05 | 0.00289377 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408419 | TGGATGGGCAGACAC[A/G]TGCCCATGGAGTTTT | 7011 |
rs774568631 | snp | A/G | 1.68712e-05 | 0.00290436 | intron-variant | TEP1 | GRCh38.p7 | 14:20396001 | AGCCGGGAGTATGGG[A/G]GGCTTCAGGGGTCCA | 7011 |
rs774571415 | snp | C/G | 1.64912e-05 | 0.00287147 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401465 | TTCTCACCTGTAACC[C/G]AGCAGGGCTTGAACG | 7011 |
rs774589395 | snp | A/G | 3.32226e-05 | 0.00407556 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376119 | CCGATCCCGGCCCCC[A/G]GTGGCCAGGCTGCCT | 7011 |
rs774610663 | snp | A/G | 6.60327e-05 | 0.00574561 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377704 | GGAGAGAGAGAAAGG[A/G]AACCCAGGTGCCCAC | 7011 |
rs774622405 | snp | A/G | 8.25321e-05 | 0.00642334 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401570 | TGACACTGTATCACC[A/G]GCCTTCTCAAACTGT | 7011 |
rs774624393 | snp | A/G | 1.64909e-05 | 0.00287144 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395526 | TTGCCATCCGAAGCT[A/G]CTGACGGCTTAGGTG | 7011 |
rs774635619 | snp | A/G | 1.65233e-05 | 0.00287426 | intron-variant | TEP1 | GRCh38.p7 | 14:20390652 | AAAATGTGGGGGAGG[A/G]AGAGGGTTTCTCAGG | 7011 |
rs774655442 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397086 | GGAACAAAATTTATG[C/G]AACACTGTTTATGGG | 7011 |
rs774661875 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408607 | TTTTCCCAGGACTGG[C/G]TTCATCCAGAGAATA | 7011 |
rs774675745 | snp | A/G | 1.66263e-05 | 0.00288321 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395606 | CGCCTCATCAGTGTT[A/G]TATTCGAAGGAAAGG | 7011 |
rs774695012 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20405032 | TTCCTTCTTTGGAAG[A/G]CCTCCTGCATCAACA | 7011 |
rs774717150 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368767 | GTGCAGGCGCACGCA[C/T]ACACACACACACACA | 7011 |
rs774794104 | snp | G/T | 1.79806e-05 | 0.00299833 | intron-variant | TEP1 | GRCh38.p7 | 14:20382386 | GGACAGCCTTGTTCA[G/T]TGCAGTGGGAGGAGA | 7011 |
rs774798682 | in-del | -/CAGAGGCCTC | 6.80052e-05 | 0.00583078 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383247 | CCAGCCGGGCCCGAG[-/CAGAGGCCTC]CAGAGGCCTCCAGAG | 7011 |
rs774828179 | snp | C/T | 3.29674e-05 | 0.00405988 | intron-variant | TEP1 | GRCh38.p7 | 14:20373671 | GAGGTGGCTGACGTT[C/T]TGTTACCTGCACGGG | 7011 |
rs774851685 | snp | C/T | 0.000122055 | 0.00781107 | intron-variant | TEP1 | GRCh38.p7 | 14:20386667 | TCTAGGGATGATTCC[C/T]ACCCCCCATCCATAG | 7011 |
rs774918492 | snp | C/T | 1.65116e-05 | 0.00287324 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385009 | CTGGAATCCCGGAAG[C/T]AGATGAGAGCTTGGG | 7011 |
rs774935136 | snp | A/G | 3.29625e-05 | 0.00405958 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373280 | CTCACCTGCTTCCTT[A/G]GGAACCTGCCAGAGC | 7011 |
rs774964090 | snp | G/T | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369532 | GGCTGCATTTGGCCA[G/T]GTTCCATAGGATCCC | 7011 |
rs775000398 | snp | A/G | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414993 | TATAAAGGAGTCTAC[A/G]GCCATACCACCCCGA | 7011 |
rs775019501 | in-del | -/GAAAAGT | 1.9344e-05 | 0.00310993 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383848 | TCAGGACGAGCCCCA[-/GAAAAGT]GGAAGAAGACTAATG | 7011 |
rs775102930 | snp | A/G | 1.65089e-05 | 0.00287301 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377487 | GACCCTGAGCCCCCT[A/G]GGAACCTAGAGAATG | 7011 |
rs775110731 | snp | A/G | 1.65987e-05 | 0.00288082 | intron-variant | TEP1 | GRCh38.p7 | 14:20406404 | AAACCAACGACCCTG[A/G]GGTAGTAGTGGCAGT | 7011 |
rs775115571 | snp | G/T | 1.66927e-05 | 0.00288895 | splice-acceptor-variant | TEP1 | GRCh38.p7 | 14:20380055 | GAGACAGGCTGGAGC[G/T]AGAGAAAGAGTAGGA | 7011 |
rs775117670 | snp | C/T | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381965 | TGGGGTAGGGGTCTC[C/T]ACTGTTACCAGCAGC | 7011 |
rs775124272 | snp | A/G | 1.65258e-05 | 0.00287448 | intron-variant | TEP1 | GRCh38.p7 | 14:20389313 | CTGGCAAAGGAAGAA[A/G]CAGTCATTAACCATC | 7011 |
rs775142696 | snp | A/G | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395925 | GAAATCTGAATGGAA[A/G]CTGCCGACTGTGGAT | 7011 |
rs775166178 | snp | C/T | 1.75234e-05 | 0.00295997 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407883 | ATTACCAAAGTTGCT[C/T]CCTGAGCTGTCTCTG | 7011 |
rs775179391 | snp | A/C | 6.60578e-05 | 0.0057467 | intron-variant | TEP1 | GRCh38.p7 | 14:20385113 | GTACTGCTGGGCCTG[A/C]GGGGAGGACAGAGAC | 7011 |
rs775194580 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397339 | CATTTATGAAACCCC[A/G]TCTCTACAAAAATAC | 7011 |
rs775197226 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20380697 | TTTGAACAAGTTTCC[G/T]AGATAGTTTTATGCT | 7011 |
rs775222757 | in-del | -/AGA | 1.82734e-05 | 0.00302264 | intron-variant | TEP1 | GRCh38.p7 | 14:20401176 | GGTCTATCATTTCAG[-/AGA]AGTCAGCAAGAAAAT | 7011 |
rs775240421 | snp | A/T | 3.29544e-05 | 0.00405908 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373125 | AGTGACGGCTGCAGA[A/T]CTCCTTGGTATACAT | 7011 |
rs775243587 | in-del | -/T | 1.64762e-05 | 0.00287016 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369695 | CAGGTTTGGCTTGAG[-/T]TATCGATATTAGGGT | 7011 |
rs775277827 | snp | A/C/G | 1.85786e-05 | 0.00304778 | intron-variant | TEP1 | GRCh38.p7 | 14:20376315 | AAAGAGGAAGCCAGA[A/C/G]AGGCCCTGGGAGGCC | 7011 |
rs775286121 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394589 | GGTTCAAGTGATTCT[C/T]CTGCCTTAGTCTCCC | 7011 |
rs775291711 | snp | C/T | 0.000165508 | 0.00909542 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373036 | GCCACAGCCTTAGCT[C/T]CCTGCCACAAGATTA | 7011 |
rs775294655 | snp | A/G | 5.02812e-05 | 0.00501379 | intron-variant | TEP1 | GRCh38.p7 | 14:20388108 | AGAATACCACAGGTC[A/G]AAATCAGTGAGGTCT | 7011 |
rs775316097 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401031 | CCCCGTAGGCTCAGC[C/T]CCCGCTCCCAGGTCT | 7011 |
rs775330962 | snp | C/G | 0.000131774 | 0.00811601 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369501 | CACATGTTACCTGTG[C/G]TCCATTCTCCTTCTG | 7011 |
rs775344669 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20390421 | CAGTAGCATCATGTC[A/G]ATAGCTTGAAATCAG | 7011 |
rs775367475 | snp | A/C | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391741 | TGTCGGTACCTGTTC[A/C]GCATCTCACCATCAT | 7011 |
rs775425177 | snp | C/G | 1.65201e-05 | 0.00287398 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384185 | GAAGGTGGCCTGGAC[C/G]AAGTCATCGTCTGGG | 7011 |
rs775445221 | snp | C/G | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368516 | TTAGCGCCCAGCCAA[C/G]GTTCCAGGCAGCTCA | 7011 |
rs775466511 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408136 | AGGAGAGGATGTCTG[G/T]GTGGGCAGAAACATG | 7011 |
rs775469563 | snp | A/C | 1.64893e-05 | 0.0028713 | intron-variant | TEP1 | GRCh38.p7 | 14:20369581 | AAATGAGGACTCTGC[A/C]ATTTTAAGGACAGAA | 7011 |
rs775472660 | snp | C/T | 5.25362e-05 | 0.00512497 | intron-variant | TEP1 | GRCh38.p7 | 14:20395674 | GCAGCTTCTATTCCC[C/T]CATCTTTTCCTACCA | 7011 |
rs775493633 | snp | C/T | 1.67225e-05 | 0.00289154 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386490 | CGCCCCAGCGGAGGT[C/T]GATTCCGTGAAGGCT | 7011 |
rs775554150 | in-del | -/T | 4.94254e-05 | 0.00497094 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408355 | TTTCTCCAAGGGCTG[-/T]TAAGTCAGGGAGCAT | 7011 |
rs775557327 | snp | A/G | 1.75388e-05 | 0.00296126 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374503 | CTGACTCTGGGTCCC[A/G]GAGCCCCACAGAGCC | 7011 |
rs775562864 | snp | C/T | 1.65326e-05 | 0.00287507 | intron-variant | TEP1 | GRCh38.p7 | 14:20382199 | TGGCCCTCAGCCTCC[C/T]AACCAACCCACCCCA | 7011 |
rs775564903 | in-del | -/TGGTTTTTTTTT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410799 | ATTGTTTCTCCTTTG[-/TGGTTTTTTTTT]TGGTTTTTTTTTTTT | 7011 |
rs775613654 | snp | C/T | 1.70699e-05 | 0.00292142 | intron-variant | TEP1 | GRCh38.p7 | 14:20380479 | GGACTGAAGAAGCTA[C/T]AAAAGGGTGGCAGAA | 7011 |
rs775624381 | snp | G/T | 0.000148377 | 0.00861198 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377390 | TTGAGTGCCCAGCCC[G/T]GCAAGGACCCATCTT | 7011 |
rs775628199 | in-del | -/GCAGC | 1.7373e-05 | 0.00294724 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383625 | GCAGCAGCCTCTGCT[-/GCAGC]TCCCACACCAGGCTT | 7011 |
rs775660326 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371292 | GGGTGGACAATATCA[C/T]AGGATTTTCTGTATA | 7011 |
rs775665199 | snp | C/T | 1.73691e-05 | 0.00294691 | intron-variant | TEP1 | GRCh38.p7 | 14:20379908 | TCAGAGGGTAAATTC[C/T]GCCCCTCCTTGATTG | 7011 |
rs775675757 | snp | A/C | 1.64977e-05 | 0.00287203 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368442 | TGGCACATCTTCATT[A/C]CCAATTCAGAAAGTA | 7011 |
rs775688614 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20413413 | GCCTGACCTGGGGCG[C/T]CCGATTCCCGCAGCA | 7011 |
rs775714724 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20399887 | CTTCATATGGCTGGG[C/T]GTGGTGGCTCACACC | 7011 |
rs775727720 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408229 | AGAGGATGTCTGGGT[A/G]GGCAGACACATATCC | 7011 |
rs775751663 | snp | A/C/T | 3.60614e-05 | 0.0042461 | intron-variant | TEP1 | GRCh38.p7 | 14:20375707 | GGGAGTGTTGTCTTG[A/C/T]CCCAGGAACCCAGCT | 7011 |
rs775794582 | snp | C/T | 6.65546e-05 | 0.00576827 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376237 | CGCGTCAGCAGCTGC[C/T]TTGGCCACAGCTGCA | 7011 |
rs775804905 | snp | C/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405486 | CCAGGAGGGCAAGTT[C/G]ACGACAGATTTCAAA | 7011 |
rs775821946 | snp | A/T | 1.6516e-05 | 0.00287362 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382267 | GGCCTGGGGAAGGAC[A/T]TCAGGCCCGTGCTCC | 7011 |
rs775858081 | snp | A/G | 1.70834e-05 | 0.00292257 | intron-variant | TEP1 | GRCh38.p7 | 14:20405618 | GGGAAGAAATGAGAA[A/G]AGAGGTAACAAGGAC | 7011 |
rs775869893 | snp | A/G | 0.000259376 | 0.0113851 | intron-variant | TEP1 | GRCh38.p7 | 14:20386437 | CCCCTCTTCTCTGCA[A/G]CCCCCACACCTGTTC | 7011 |
rs775947000 | snp | A/G | 0.000148523 | 0.00861624 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380257 | GATTTTTCATGGTCC[A/G]GGGTTTATTAAGCCA | 7011 |
rs775947140 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367420 | CAGAGTTCATGGCTA[C/T]GATTGTGCCACCTCT | 7011 |
rs775948129 | snp | A/G | 6.59022e-05 | 0.00573993 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384604 | CCTCAGCTCACCTGC[A/G]GCAGGTGATCCCTTT | 7011 |
rs775997271 | snp | G/T | 3.29587e-05 | 0.00405934 | intron-variant | TEP1 | GRCh38.p7 | 14:20373499 | CTCTGGTCCTTGCAG[G/T]AACTCACCAAGAGTG | 7011 |
rs776038163 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387949 | TGGAGTGTCCTCTTC[C/T]AGTGGCCGGAGAGAC | 7011 |
rs776058844 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20412863 | AGGGTTTTCACCATG[G/T]TGGTCAGGCTGGTCT | 7011 |
rs776064562 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20381302 | GGTGTCTATGGGGTC[C/T]AGGAACTAACCAGGT | 7011 |
rs776093131 | in-del | -/AGA | 3.53744e-05 | 0.00420547 | intron-variant | TEP1 | GRCh38.p7 | 14:20408466 | AGCTTGTATATGCCT[-/AGA]AGGAGAGAAAGACAG | 7011 |
rs776112016 | snp | A/G | 1.65605e-05 | 0.0028775 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379095 | CAGCCACTCACCACA[A/G]ACTTCTCCTCCTGCG | 7011 |
rs776135495 | snp | C/T | 6.59457e-05 | 0.00574182 | synonymous-codon, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381554 | TGGGCTGCAATCACC[C/T]GCAATGAGGATGTGT | 7011 |
rs776159689 | snp | A/T | 1.75841e-05 | 0.00296509 | intron-variant | TEP1 | GRCh38.p7 | 14:20391144 | CCCCTGCTTTGGAAT[A/T]CACCCTTGCCCAGCC | 7011 |
rs776202363 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20409987 | AGATTGGCCACTGCA[C/G]TCCAGCCTGGGCGAC | 7011 |
rs776202811 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400790 | TGGTATAATGATCTA[C/T]GATGCCAACATTACT | 7011 |
rs776256664 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372756 | TCCGGGTGCCGAACC[C/G]TTCCGCAGTTTCACT | 7011 |
rs776274921 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403751 | GGCCGGCGGGGGTGT[C/T]TCTTGGCCCGGTGCT | 7011 |
rs776275398 | snp | A/G | 1.65875e-05 | 0.00287984 | intron-variant | TEP1 | GRCh38.p7 | 14:20386060 | CCAGCCCTCCTCCAA[A/G]CCTGTCTGCCTTACC | 7011 |
rs776298154 | snp | C/G | 8.24423e-05 | 0.00641984 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391073 | CATCATCCCAATCAA[C/G]AGCAGTGCATAGTTC | 7011 |
rs776309465 | snp | G/T | 5.16187e-05 | 0.00508003 | intron-variant | TEP1 | GRCh38.p7 | 14:20371653 | TCAAAAAAGTACATG[G/T]ACAGAGAAAGATCCT | 7011 |
rs776324645 | snp | G/T | 1.94623e-05 | 0.00311942 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383905 | GGAGCCTGCAGGGCT[G/T]ACACAAGAGATGCCT | 7011 |
rs776371518 | snp | A/C | 1.6681e-05 | 0.00288794 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407922 | ATGGATTTCAGGGCT[A/C]TAGGGCAGGTTGAAA | 7011 |
rs776372732 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20391811 | GGCTCAGGGACTTAT[A/C]TGCCCCTTAGAGGCA | 7011 |
rs776378524 | snp | C/T | 4.94271e-05 | 0.00497102 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369702 | GGCTTGAGTTATCGA[C/T]ATTAGGGTCCTACTA | 7011 |
rs776382470 | snp | A/T | 1.75068e-05 | 0.00295857 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396669 | GTGGCGGGAACTGAT[A/T]CCAACCCGCAGCAGG | 7011 |
rs776397344 | snp | A/G | 1.65789e-05 | 0.0028791 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376127 | GGCCCCCGGTGGCCA[A/G]GCTGCCTCCATCAGT | 7011 |
rs776405130 | snp | A/G/T | 1.64792e-05 | 0.00287042 | missense, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20388024 | GTCCATTTGGCCCAC[A/G/T]TGTTCCAGAAGATGG | 7011 |
rs776411232 | snp | C/G | 1.7318e-05 | 0.00294256 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368876 | CTCAGGTAGCACATG[C/G]AGGGCTGTGACAGAG | 7011 |
rs776430504 | snp | C/T | 1.65031e-05 | 0.00287251 | intron-variant | TEP1 | GRCh38.p7 | 14:20369636 | CCATCCACCCTGGGC[C/T]ATCTCCCGGCTCCTC | 7011 |
rs776444186 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20404147 | ATCACCTGAGGTCAG[A/G]CGTTCAAGACCAGCC | 7011 |
rs776447187 | snp | A/C/T | 4.95883e-05 | 0.00497917 | intron-variant | TEP1 | GRCh38.p7 | 14:20385122 | GGCCTGCGGGGAGGA[A/C/T]AGAGACAGTGAGTTT | 7011 |
rs776448663 | snp | C/T | 1.72204e-05 | 0.00293427 | intron-variant | TEP1 | GRCh38.p7 | 14:20395423 | CCCCGATTGCCCACC[C/T]TTGGCTCCCAGACAG | 7011 |
rs776455935 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382652 | TGAAGAGCCTCAGGT[A/G]ATCGGTGACCAAGCG | 7011 |
rs776465334 | snp | C/T | 3.29951e-05 | 0.00406159 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381977 | CTCCACTGTTACCAG[C/T]AGCCACTGCTTCTTC | 7011 |
rs776472678 | snp | A/G | 1.73622e-05 | 0.00294632 | intron-variant | TEP1 | GRCh38.p7 | 14:20401154 | TATCTGAGGATAGGT[A/G]AGAAAGAGGTCTATC | 7011 |
rs776493679 | snp | A/T | 1.65141e-05 | 0.00287346 | intron-variant | TEP1 | GRCh38.p7 | 14:20377497 | CCCCTGGGAACCTAG[A/T]GAATGAGAGAGAACA | 7011 |
rs776504339 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384477 | CAACATAGGGCCGGC[C/T]AGCTGCCACACCCCC | 7011 |
rs776512569 | snp | A/C | 1.65291e-05 | 0.00287476 | intron-variant | TEP1 | GRCh38.p7 | 14:20389334 | ATTAACCATCACAAA[A/C]AATACCTGGAACACA | 7011 |
rs776522963 | snp | A/G | 1.66746e-05 | 0.00288739 | intron-variant | TEP1 | GRCh38.p7 | 14:20406425 | TAGTGGCAGTTATGA[A/G]TCACAGCAGGTATCC | 7011 |
rs776564934 | snp | C/T | 1.651e-05 | 0.0028731 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389686 | AGTAAAGCTGTTTGG[C/T]CACATTTATCATTCC | 7011 |
rs776620098 | snp | C/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380385 | AGCCGGGGGTACTGG[C/G]TGAGGATTGAAGCCT | 7011 |
rs776636689 | snp | A/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390984 | TTCAGGATGCCTTCT[A/T]CTGCCTTAAGCACTG | 7011 |
rs776649005 | snp | C/T | 4.94205e-05 | 0.0049707 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401057 | GGTCTCTGGCCTAGA[C/T]AGCTTCATCCTCTTC | 7011 |
rs776649262 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373140 | ACTCCTTGGTATACA[C/T]GTGTCATCTGGAGGA | 7011 |
rs776686435 | snp | C/T | 3.64365e-05 | 0.00426813 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383323 | CCCCTAGGCCTGCAT[C/T]ACTAGACACACTCAG | 7011 |
rs776712849 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408898 | CTCATAAGAAGGTAA[A/G]GGAGACCCAACCCCC | 7011 |
rs776733885 | snp | C/T | 1.76232e-05 | 0.00296838 | intron-variant | TEP1 | GRCh38.p7 | 14:20375728 | GAACCCAGCTGGGCT[C/T]TGTGCCACCCCTGGC | 7011 |
rs776756458 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373062 | GATTAGTTCCCCAGC[C/T]TGATTTCCAGATACT | 7011 |
rs776759410 | snp | C/T | 1.65427e-05 | 0.00287595 | intron-variant | TEP1 | GRCh38.p7 | 14:20378725 | CATGGCTCAGGGCCA[C/T]TCTGACCACTGCAGA | 7011 |
rs776788151 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20370063 | GGAACACCGGCGTGC[A/G]CCACCACACCCAGCT | 7011 |
rs776813094 | snp | A/G | 3.30513e-05 | 0.00406504 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378063 | TAACTGGCAACCCGC[A/G]TGCAGGAAAAGCGCA | 7011 |
rs776813215 | snp | C/T | 1.68675e-05 | 0.00290405 | intron-variant | TEP1 | GRCh38.p7 | 14:20395636 | GGCAATGCTGTATGA[C/T]GACAGGTAAATTTCC | 7011 |
rs776817136 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408244 | GGGCAGACACATATC[C/T]ATGTGGTTTTTCCAT | 7011 |
rs776819992 | snp | C/T | 1.73114e-05 | 0.002942 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382350 | GGGTCCGGAGTCTCT[C/T]AGACACCTAGGATGG | 7011 |
rs776836247 | snp | A/G | 1.64738e-05 | 0.00286995 | intron-variant | TEP1 | GRCh38.p7 | 14:20371318 | GTATAGCTGCTCCTG[A/G]TTTGTGAGAAAGGAA | 7011 |
rs776842716 | snp | A/C | 1.80667e-05 | 0.0030055 | intron-variant | TEP1 | GRCh38.p7 | 14:20404801 | TGAGAGGACTAGAAT[A/C]TCAGTCACTCCTCCC | 7011 |
rs776851851 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406258 | TGAAGGACATGGTCA[A/G]TAGGCTCTGGATGAG | 7011 |
rs776870797 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408348 | TGATGTAGTTTCTCC[A/G]AGGGCTGTAAGTCAG | 7011 |
rs776911791 | snp | C/T | 8.556e-05 | 0.00654008 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386456 | CCACACCTGTTCCTA[C/T]GGGTCTCCTCCTCAG | 7011 |
rs776914763 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375235 | TGGAGTGCAATGGCG[C/T]GACCTCTGCCTCCCG | 7011 |
rs776932809 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20386286 | ACGGGGCCCTGACTC[A/G]CAACTGAGTAAAGAA | 7011 |
rs776940719 | snp | C/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403235 | CACATGCCTTTCCCA[C/G]TGCTCTCAGAACCTT | 7011 |
rs776974237 | snp | A/G | 8.30461e-05 | 0.0064433 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401610 | CCCAAGTCCCACAGG[A/G]GTCCTTTCATCCATG | 7011 |
rs776982793 | snp | G/T | 3.29848e-05 | 0.00406095 | intron-variant | TEP1 | GRCh38.p7 | 14:20383666 | ATGGAGAGGAAGTCA[G/T]GGTCAGTGGGAGAGA | 7011 |
rs777002497 | snp | A/G | 1.64776e-05 | 0.00287028 | intron-variant | TEP1 | GRCh38.p7 | 14:20373622 | CAGAAGAAGGGACGG[A/G]GCAGGGGAGAAAAGA | 7011 |
rs777006678 | snp | G/T | 3.30786e-05 | 0.00406672 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376199 | GCTCAGTGCCACAGG[G/T]AAAGTCTTCTGCCTT | 7011 |
rs777016119 | snp | C/T | 1.64819e-05 | 0.00287066 | intron-variant | TEP1 | GRCh38.p7 | 14:20384345 | GGACAACCCAGACCA[C/T]CCCATGTCCCTCTCC | 7011 |
rs777068772 | snp | G/T | 0.000115461 | 0.00759718 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368451 | TTCATTCCCAATTCA[G/T]AAAGTACACATTGCC | 7011 |
rs777079242 | snp | C/G | 1.66643e-05 | 0.0028865 | intron-variant | TEP1 | GRCh38.p7 | 14:20379114 | TCTCCTCCTGCGACA[C/G]TGGGTGAGGGAGCGC | 7011 |
rs777116233 | in-del | -/GCAC | 1.65132e-05 | 0.00287339 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373769 | TGATGGTCCCACACT[-/GCAC]TTCAAGGTCCCATCC | 7011 |
rs777133526 | snp | C/T | 4.94425e-05 | 0.0049718 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395904 | CAATGGCATCATGGG[C/T]GTTAAGAAATCTGAA | 7011 |
rs777150056 | snp | C/T | 1.65149e-05 | 0.00287353 | intron-variant | TEP1 | GRCh38.p7 | 14:20380927 | AGCCAGTGACTCATC[C/T]CACCATAGAGGGCAT | 7011 |
rs777153358 | snp | C/T | 1.67478e-05 | 0.00289372 | intron-variant | TEP1 | GRCh38.p7 | 14:20395812 | TGCTGCTTCATTTAT[C/T]GTCAGATGTGGGAGG | 7011 |
rs777161740 | snp | C/T | 1.65693e-05 | 0.00287826 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384985 | GGCAACAGACAGTAC[C/T]TGAGGAAGCTGGAAT | 7011 |
rs777173062 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20413099 | GCACACAGGGCAAGG[A/G]AGTAAGAGGGGATGA | 7011 |
rs777176655 | snp | A/G | 1.67494e-05 | 0.00289386 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375777 | TTATCTTTGGTCCAG[A/G]CACAGCCAGTGACCC | 7011 |
rs777189689 | snp | A/G | 1.65663e-05 | 0.002878 | intron-variant | TEP1 | GRCh38.p7 | 14:20388076 | AACCTGACATAAATA[A/G]CAAGATAAATGAGAG | 7011 |
rs777199327 | snp | A/G | 4.95946e-05 | 0.00497944 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404688 | GTCGCAGGTGGGGGC[A/G]ACACGCCGGCAAGAA | 7011 |
rs777213576 | snp | A/G | 4.95405e-05 | 0.00497673 | intron-variant | TEP1 | GRCh38.p7 | 14:20390896 | TATTCCCAGGCCTGT[A/G]TCCTTCATGTATTTT | 7011 |
rs777214920 | snp | C/T | 4.0858e-05 | 0.00451966 | intron-variant | TEP1 | GRCh38.p7 | 14:20383719 | TGGGCATCAACAAGG[C/T]TGGGCTCATTGGGGG | 7011 |
rs777244307 | in-del | -/C | 0.000395844 | 0.0140629 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384487 | CGGCCAGCTGCCACA[-/C]CCCCCCCACTCACAG | 7011 |
rs777251746 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408217 | GGTTCTCCAAGGAGA[A/G]GATGTCTGGGTGGGC | 7011 |
rs777271954 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393078 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGTGCCT | 7011 |
rs777277505 | snp | A/T | 1.72403e-05 | 0.00293596 | intron-variant | TEP1 | GRCh38.p7 | 14:20379914 | GGTAAATTCTGCCCC[A/T]CCTTGATTGTCATAC | 7011 |
rs777291701 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394923 | AAGATACTGATGAAC[C/T]ACTTAAAAAGACAGC | 7011 |
rs777312950 | snp | C/T | 2.35253e-05 | 0.00342959 | intron-variant | TEP1 | GRCh38.p7 | 14:20374566 | GTCAGAGGAGTGGGA[C/T]TATCAGCATCCCTCC | 7011 |
rs777324913 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403513 | GAAGAGATCCAGTCA[A/G]TAGCCCTGAAGGTGC | 7011 |
rs777327762 | snp | C/G | 1.74318e-05 | 0.00295222 | intron-variant | TEP1 | GRCh38.p7 | 14:20386404 | GTCCACCACTCAAGC[C/G]CCTCATCCCCGACCC | 7011 |
rs777332859 | in-del | -/AT | 1.68698e-05 | 0.00290424 | intron-variant | TEP1 | GRCh38.p7 | 14:20369815 | TTGTTTAGCCTACCC[-/AT]ATGAGTCAACTTGTA | 7011 |
rs777346448 | snp | C/T | 3.36836e-05 | 0.00410374 | intron-variant | TEP1 | GRCh38.p7 | 14:20378576 | GATGCTGAAGAGAGA[C/T]GCCTGAACTTCTCAG | 7011 |
rs777363099 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384651 | CTCTTCAGTTCTGAG[A/G]TCCGACGTGCGGCCT | 7011 |
rs777387656 | snp | C/G | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381631 | CTGTTCTCAGGGGCC[C/G]ATCAGGGAGGCACAG | 7011 |
rs777393703 | snp | A/C | 1.64727e-05 | 0.00286986 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371271 | CAAATATGCCATACT[A/C]CTTGTGGGTGGACAA | 7011 |
rs777430504 | snp | A/T | 1.6722e-05 | 0.00289149 | intron-variant | TEP1 | GRCh38.p7 | 14:20384258 | ATGGGTCAGTGACTA[A/T]CCATGGTGCCATGCT | 7011 |
rs777440296 | snp | C/G | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377687 | GTGCCACAGAGAGGG[C/G]AGGAGAGAGAGAAAG | 7011 |
rs777444391 | snp | A/G | 1.70784e-05 | 0.00292214 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404748 | CATTCCGGACGTTCA[A/G]CTGCTGCCTGGCATA | 7011 |
rs777460686 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372526 | ATCTGTAACTGGTTC[A/G]TACTGCCTGGCCCAG | 7011 |
rs777500936 | snp | A/G | 1.65209e-05 | 0.00287405 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379076 | ACAAGCAGAGATTCC[A/G]TCACAGCCACTCACC | 7011 |
rs777541865 | in-del | -/ACAG | 1.64844e-05 | 0.00287087 | intron-variant | TEP1 | GRCh38.p7 | 14:20372979 | CAGGGTAGAATTCAC[-/ACAG]ACAAAGAACCAAGGG | 7011 |
rs777553918 | snp | A/C | 3.39092e-05 | 0.00411746 | intron-variant | TEP1 | GRCh38.p7 | 14:20379156 | TCCCCTTGACCCTCC[A/C]AGTCCCACCACTCCA | 7011 |
rs777586109 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391716 | GAGGTTCACAGCTGT[C/G]TCTAGGGCCTGTCGG | 7011 |
rs777621271 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408112 | GGGTGGCCAGGCACC[A/G]GTTCTCCAAGGAGAG | 7011 |
rs777621949 | snp | A/T | 1.65343e-05 | 0.00287521 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368412 | TCTAGCACAAGGGGT[A/T]TCATTATTCCCGAGT | 7011 |
rs777626989 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369443 | GCAGGTAGATGGGTC[C/T]GTCCCTGGAGTTTGG | 7011 |
rs777656086 | snp | A/G | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415491 | CCCAGCACTTTGGGA[A/G]GCCAAGGTGGGCAGA | 7011 |
rs777679304 | snp | C/T | 6.60906e-05 | 0.00574812 | intron-variant | TEP1 | GRCh38.p7 | 14:20378262 | AGGTAGAAATGGAAA[C/T]GTGAAGACCTGCTCT | 7011 |
rs777701266 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368887 | ATGGAGGGCTGTGAC[-/A]AGAGCCCGAGTGAAT | 7011 |
rs777727282 | snp | A/G | 3.2969e-05 | 0.00405998 | intron-variant | TEP1 | GRCh38.p7 | 14:20373460 | ACAGAAGGTTATTCC[A/G]CATACCTTCCCCACC | 7011 |
rs777745919 | snp | A/G | | | | | GRCh38.p7 | 14:20416517 | GAGTAGGACCCAGGC[A/G]TCAGTAGTTTTTGAA | 7011 |
rs777751123 | snp | A/C | 0.000137285 | 0.00828393 | intron-variant | TEP1 | GRCh38.p7 | 14:20384752 | TTGGAATAGACTCAG[A/C]CCCCAGCCAGCCTCC | 7011 |
rs777754408 | snp | A/G | 1.73972e-05 | 0.00294929 | intron-variant | TEP1 | GRCh38.p7 | 14:20377780 | GAAAAGGGCTTAAGG[A/G]TACCACCTCCACCAC | 7011 |
rs777755594 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403372 | CCCCAGAAGAAGGGA[C/T]TCACCTTTCTCTGCT | 7011 |
rs777777702 | snp | A/C | 0.00018131 | 0.00951957 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390743 | TCAGGGACCATCCAT[A/C]ATTTTCATCAAACTC | 7011 |
rs777788820 | snp | C/T | 2.5068e-05 | 0.00354025 | intron-variant | TEP1 | GRCh38.p7 | 14:20368929 | AAGGGGAGAGCAGAA[C/T]GGTGAGTTCTCAGGG | 7011 |
rs777818696 | snp | A/G | 6.59076e-05 | 0.00574016 | intron-variant | TEP1 | GRCh38.p7 | 14:20371440 | GATAACCACTAACTC[A/G]GGTTTCCTTTTTCCC | 7011 |
rs777837648 | snp | C/G | 0.000291163 | 0.0120622 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383613 | CAGCAGACTTGGGCA[C/G]CAGCCTCTGCTGCAG | 7011 |
rs777837972 | snp | C/T | 1.67511e-05 | 0.00289401 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368855 | CTTCGAAGCTGTCAC[C/T]AGCAACTCAGGTAGC | 7011 |
rs777840205 | snp | C/T | 3.29473e-05 | 0.00405864 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372822 | AAAAAAGGTGTGTGC[C/T]GAGGACCAGATCAGA | 7011 |
rs777877711 | snp | C/G | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387918 | ACCCTTGCTGGGAAA[C/G]AGGAGCCAAGGGGCT | 7011 |
rs777894635 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20382113 | CCATACGGTGTCCCC[A/G]CCCCCACCACACCCA | 7011 |
rs777894748 | snp | C/G | 4.0681e-05 | 0.00450986 | intron-variant | TEP1 | GRCh38.p7 | 14:20383690 | GGAGAGAAAAAAAAA[C/G]CAGGGGTGGTACGTG | 7011 |
rs777909204 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374220 | TCAGCCTCCTGAGTA[A/G]CTAGAACTACAGGCA | 7011 |
rs777927900 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378399 | GTGACTTTGAGCCCA[C/T]CCACCTGGAAGAAGC | 7011 |
rs777929511 | in-del | -/ATTTTACTAC | | | intron-variant | TEP1 | GRCh38.p7 | 14:20390293 | TATAACTTCCTAATA[-/ATTTTACTAC]ATTTTACTATTATCT | 7011 |
rs777951019 | snp | C/T | 1.66051e-05 | 0.00288137 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391602 | TTGTTTTCTTACCCC[C/T]TGTGGGTTGCTCTTT | 7011 |
rs777974255 | snp | C/G | 1.64961e-05 | 0.00287189 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373715 | TGCACAGTGGCTAAT[C/G]GGTCCTGAGTGAGCA | 7011 |
rs778018529 | snp | C/T | 1.6557e-05 | 0.00287719 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376209 | ACAGGGAAAGTCTTC[C/T]GCCTTGTGTGGCCGC | 7011 |
rs778024122 | snp | C/G | 5.02803e-05 | 0.00501374 | intron-variant | TEP1 | GRCh38.p7 | 14:20386647 | AAGCAGAGAGCTGGG[C/G]TCAGTCTAGGGATGA | 7011 |
rs778050046 | snp | A/G | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407977 | GAGCCCTCCAACTTG[A/G]AGGCTCAGAGAGCAG | 7011 |
rs778056728 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382681 | CGCAGGTAGAGCGGC[C/T]GGCCTGATTCCCGCT | 7011 |
rs778059884 | snp | C/G | 1.6498e-05 | 0.00287206 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381957 | CGGGCCCATGGGGTA[C/G]GGGTCTCCACTGTTA | 7011 |
rs778102552 | in-del | -/C | 3.54622e-05 | 0.00421068 | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20407872 | TGCCTGGAGCTATTA[-/C]CAAAGTTGCTTCCTG | 7011 |
rs778112993 | snp | C/T | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382019 | TCCCCTTCGGTAGTG[C/T]CCGCCACACACTCAG | 7011 |
rs778157113 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411168 | AAGGTAAGGGCTCCT[A/T]TGTCTTGCTCCCCTC | 7011 |
rs778169483 | in-del | -/T | 0.000214159 | 0.0103457 | intron-variant | TEP1 | GRCh38.p7 | 14:20382609 | TTAGGACTTGGAAGG[-/T]GATGAGAACTGACCT | 7011 |
rs778175315 | snp | C/T | 1.648e-05 | 0.0028705 | intron-variant | TEP1 | GRCh38.p7 | 14:20377577 | CTAAAGGCTCAAAAA[C/T]CCACCCATTCCCATT | 7011 |
rs778195714 | snp | C/G | 1.79387e-05 | 0.00299483 | intron-variant | TEP1 | GRCh38.p7 | 14:20407854 | GGCTGGAGTCAAGAT[C/G]AGTGCCTGGAGCTAT | 7011 |
rs778199921 | snp | A/G | 1.68772e-05 | 0.00290488 | intron-variant | TEP1 | GRCh38.p7 | 14:20380220 | GCTTACTAGGGTCTG[A/G]GGTCAAGGTCTTACC | 7011 |
rs778207815 | snp | A/G | | | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401542 | GGGTGAACCTTGGAG[A/G]ATTCTTTTTCTCTGA | 7011 |
rs778210542 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373364 | AGCAGCAGCACGGAC[C/T]GGGCCGCTGTGTCCC | 7011 |
rs778221870 | snp | C/T | 1.67444e-05 | 0.00289343 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386525 | CGGTGAGGGGCCGCT[C/T]GGGCCTGCAGTGCTG | 7011 |
rs778228274 | snp | A/G | 1.6676e-05 | 0.00288751 | intron-variant | TEP1 | GRCh38.p7 | 14:20373820 | CTCCTCCTGCCCACA[A/G]AGCACAAGATCAGAG | 7011 |
rs778252346 | snp | A/G | 1.64876e-05 | 0.00287116 | intron-variant | TEP1 | GRCh38.p7 | 14:20373219 | ATCAGGCCACCCTTG[A/G]CCTTTTTTTGTGCCA | 7011 |
rs778254546 | in-del | -/TCACTATCCATGCTGGCA | 0.000329459 | 0.0128305 | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369380 | AGATGTGGTGTTGGC[-/TCACTATCCATGCTGGCA]TCACTATCCATGCTG | 7011 |
rs778267409 | snp | A/C | 4.95258e-05 | 0.00497599 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389620 | CTTACAGGTATTGTA[A/C]CCTTCTTAGGAGGAT | 7011 |
rs778269815 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368119 | GGGTCCTAGGGCCCG[C/T]GAGTGATGCAAGAAT | 7011 |
rs778270204 | snp | A/G | 1.75366e-05 | 0.00296108 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396626 | TCACACATACCGCAT[A/G]CTGGAGTCTCTGGAG | 7011 |
rs778309761 | snp | A/G/T | 6.62278e-05 | 0.00575414 | intron-variant | TEP1 | GRCh38.p7 | 14:20403694 | CTGGAGAAAAGGGGC[A/G/T]TGGGTCGAGGGCTGG | 7011 |
rs778376816 | snp | A/C | 1.68519e-05 | 0.0029027 | intron-variant | TEP1 | GRCh38.p7 | 14:20376077 | AGAGGCTATGGGACC[A/C]CAGGGTTGCATCCTT | 7011 |
rs778453156 | snp | C/T | 4.94295e-05 | 0.00497115 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369563 | ATCAGAGCTGGCACA[C/T]AAAAATGAGGACTCT | 7011 |
rs778457842 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386118 | TTGTAGCTGGGGGGA[A/G]TGTATCCATAACGGG | 7011 |
rs778475957 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372301 | CTACTCATTCTGTAA[C/G]TGTCCAACCTTAAAT | 7011 |
rs778490963 | snp | A/G | 3.32386e-05 | 0.00407654 | intron-variant | TEP1 | GRCh38.p7 | 14:20401408 | CACGGATGTTGAAAA[A/G]TTAAGGAATTACTTA | 7011 |
rs778532415 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368497 | GGCAAGCTGCAGGGT[A/G]GAGTTAGCGCCCAGC | 7011 |
rs778546954 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374759 | AATGATAATGTACCT[-/A]ATCTGATATGGTGGT | 7011 |
rs778563144 | in-del | -/TACA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368786 | ACACACACACACACA[-/TACA]CACACACTTACCAGC | 7011 |
rs778578770 | snp | A/G | 9.8974e-05 | 0.007034 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378800 | AGCAGCCGGCAGTCT[A/G]GGCTCAGGCAGCAGC | 7011 |
rs778581086 | snp | A/G | 1.79393e-05 | 0.00299488 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383302 | CCTGGCTCTGCTCAA[A/G]GGTCTCCCCTAGGCC | 7011 |
rs778633207 | snp | C/T | 1.65241e-05 | 0.00287433 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395488 | CTCCCTCTTGAGCTG[C/T]TCATACAACACAGGT | 7011 |
rs778636695 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398072 | GTTTCTTAATAATAA[C/T]ATTTTTAAGGTTTAT | 7011 |
rs778644662 | snp | C/T | 0.000144191 | 0.00848968 | intron-variant | TEP1 | GRCh38.p7 | 14:20377792 | AGGATACCACCTCCA[C/T]CACGCGGTCCTCCTT | 7011 |
rs778699655 | snp | A/G | 3.3151e-05 | 0.00407117 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378046 | TCCTCTCCAGCCGTC[A/G]GTAACTGGCAACCCG | 7011 |
rs778703715 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408221 | CTCCAAGGAGAGGAT[A/G]TCTGGGTGGGCAGAC | 7011 |
rs778720394 | in-del | -/A | 1.75081e-05 | 0.00295867 | | | GRCh38.p7 | 14:20377271 | CCCTGCCCACTGTCT[-/A]AGTAGTACCTGAGGC | 7011 |
rs778735779 | snp | G/T | | | | | GRCh38.p7 | 14:20416617 | ATATTAAGGGTTGGG[G/T]TCTTTAGGAGGGATT | 7011 |
rs778750584 | snp | C/T | | | | | GRCh38.p7 | 14:20371905 | CCTGTGGATGCAACA[C/T]ATGCCTAAATCCGTA | 7011 |
rs778774549 | snp | C/T | 1.64814e-05 | 0.00287061 | intron-variant | TEP1 | GRCh38.p7 | 14:20378896 | CTGGACCCTGGCCAT[C/T]AGCTCCCTCCTCATT | 7011 |
rs778831076 | snp | A/G | 0.00012565 | 0.00792521 | intron-variant | TEP1 | GRCh38.p7 | 14:20376303 | AACAGCTTCCTGAAA[A/G]AGGAAGCCAGACAGG | 7011 |
rs778857745 | snp | A/C | 1.66513e-05 | 0.00288537 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405580 | CAGCAAGCTCAGTAG[A/C]GCCATCTGGGAATTG | 7011 |
rs778859947 | in-del | -/GCTGGGATACT | 3.29723e-05 | 0.00406018 | intron-variant | TEP1 | GRCh38.p7 | 14:20373178 | CGTGTTTCATTAGGA[-/GCTGGGATACT]GCTGGGATAAGAGAT | 7011 |
rs778862459 | snp | C/G | 1.64735e-05 | 0.00286993 | intron-variant | TEP1 | GRCh38.p7 | 14:20371474 | CTCAGGAGGAAATGG[C/G]ATTTTGGATCTTACC | 7011 |
rs778908024 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400632 | TCCTAAATACAATAT[A/G]AGGTTCTGTACAGAT | 7011 |
rs778909540 | snp | A/C | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390753 | TCCATCATTTTCATC[A/C]AACTCCTGAAGGAAA | 7011 |
rs778950027 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20385819 | AGGGAGATCAGTACC[C/G]AGATCTATCTGATGG | 7011 |
rs778960243 | snp | C/G | 5.14161e-05 | 0.00507005 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382333 | GGGGACAGTGGCAGG[C/G]AGGGTCCGGAGTCTC | 7011 |
rs778962869 | snp | A/G | 3.29946e-05 | 0.00406155 | intron-variant | TEP1 | GRCh38.p7 | 14:20390924 | TTTTGGATGGTGGGT[A/G]TTGAGTGTCTGACCT | 7011 |
rs778965885 | snp | A/C | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406334 | CCTCCTCCTCTCCCA[A/C]GCTCAGACTATAAGA | 7011 |
rs779086209 | snp | A/C | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20388023 | TGTCCATTTGGCCCA[A/C]ATGTTCCAGAAGATG | 7011 |
rs779089432 | snp | A/G | 3.45077e-05 | 0.00415363 | intron-variant | TEP1 | GRCh38.p7 | 14:20382760 | CCAGGAGGGCTGCCC[A/G]CAGCCAGCCCTCTGC | 7011 |
rs779107793 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388737 | GAATTATGAGGTAGA[A/G]GCTGAGTATTTGAGG | 7011 |
rs779137678 | snp | A/T | 1.68038e-05 | 0.00289855 | intron-variant | TEP1 | GRCh38.p7 | 14:20384953 | CTGGCCTTTTGGGGA[A/T]GGAGCCCCAGCCTGC | 7011 |
rs779157374 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403389 | CACCTTTCTCTGCTC[C/T]TCTCTGAGAAACCCT | 7011 |
rs779195154 | in-del | -/CAGCAGTG | | | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391073 | CATCATCCCAATCAA[-/CAGCAGTG]CATAGTTCAGCGGGG | 7011 |
rs779196374 | in-del | -/CG/CGCG | 0.00282744 | 0.0374981 | intron-variant | TEP1 | GRCh38.p7 | 14:20368762 | AGGTGTGCAGGCGCA[-/CG/CGCG]CGCACACACACACAC | 7011 |
rs779214026 | snp | A/C | 1.6476e-05 | 0.00287014 | intron-variant | TEP1 | GRCh38.p7 | 14:20373587 | CAGGCTGTCCAGCTG[A/C]TAAGACACAGAGACT | 7011 |
rs779238142 | snp | A/C | 0.000165604 | 0.00909805 | intron-variant | TEP1 | GRCh38.p7 | 14:20396737 | TCCCATTTTCTGTGG[A/C]ATGTGGGGCATAGAG | 7011 |
rs779241628 | in-del | -/AGGGG | 1.6861e-05 | 0.00290348 | intron-variant | TEP1 | GRCh38.p7 | 14:20391114 | GATTGGACAAGTGTC[-/AGGGG]AAATAAAGCTCCCCT | 7011 |
rs779253361 | snp | A/G | 1.74753e-05 | 0.0029559 | intron-variant | TEP1 | GRCh38.p7 | 14:20379899 | CATGGATTTTCAGAG[A/G]GTAAATTCTGCCCCT | 7011 |
rs779279205 | snp | A/C | 1.64754e-05 | 0.00287009 | intron-variant | TEP1 | GRCh38.p7 | 14:20386230 | GACGTGTGGGAGTCA[A/C]TGGGGGCATGGTATC | 7011 |
rs779291569 | snp | A/T | 1.65064e-05 | 0.00287279 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391620 | TGGGTTGCTCTTTGG[A/T]CAGAGCCTGTCTGCA | 7011 |
rs779342824 | snp | A/G | 4.94173e-05 | 0.00497053 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371288 | TTGTGGGTGGACAAT[A/G]TCATAGGATTTTCTG | 7011 |
rs779375197 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | TEP1 | GRCh38.p7 | 14:20384548 | GGTCAGAGCAGGCCC[A/G]GCTCCTCTCACCACA | 7011 |
rs779376383 | snp | C/G | 1.72549e-05 | 0.0029372 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396641 | GCTGGAGTCTCTGGA[C/G]AATGAGCTCATGGTG | 7011 |
rs779402043 | snp | C/T | 3.60419e-05 | 0.00424495 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374429 | CCATTGCTTTCTCAC[C/T]ACAGCTGCCACAGCG | 7011 |
rs779405382 | in-del | -/TAGC | 1.64754e-05 | 0.00287009 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384633 | TTCTGTCTGCTTAGG[-/TAGC]TCTTCAGTTCTGAGA | 7011 |
rs779443307 | snp | C/T | 4.95078e-05 | 0.00497508 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379048 | GAAAGAGTGTATCAT[C/T]GGAGAGGAACAAACA | 7011 |
rs779458389 | snp | A/G | 1.65307e-05 | 0.0028749 | intron-variant | TEP1 | GRCh38.p7 | 14:20403900 | CTGTCAAAGAGAGAG[A/G]AGAGACCACTAGAAG | 7011 |
rs779465930 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20399162 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 7011 |
rs779496925 | snp | A/G | 1.66896e-05 | 0.00288869 | intron-variant | TEP1 | GRCh38.p7 | 14:20369796 | TGTGAAAGAATAGGT[A/G]ATTTTGTTTAGCCTA | 7011 |
rs779552077 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373327 | CAGAGGCGGTCAGCA[C/T]GAGGCCTGAGGTTTC | 7011 |
rs779552771 | snp | A/G | 1.72555e-05 | 0.00293725 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384058 | AGGCTGTCTTGCCCT[A/G]TCCTGACTGCCCCGT | 7011 |
rs779561066 | snp | C/T | 1.80247e-05 | 0.003002 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383308 | TCTGCTCAAGGGTCT[C/T]CCCTAGGCCTGCATC | 7011 |
rs779605391 | snp | C/G | 1.64754e-05 | 0.00287009 | missense, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401518 | GCAGTCGCTGAACCA[C/G]CTTCTTCAGGGTGAA | 7011 |
rs779605418 | snp | C/T | 3.30186e-05 | 0.00406303 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384132 | GTGTCCTGAAGAAGG[C/T]GTGGCCGGGCAGGAC | 7011 |
rs779605603 | snp | A/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382689 | GAGCGGCCGGCCTGA[A/T]TCCCGCTTCACCAGC | 7011 |
rs779642976 | snp | A/G | 1.67508e-05 | 0.00289398 | intron-variant | TEP1 | GRCh38.p7 | 14:20373835 | GAGCACAAGATCAGA[A/G]CAGAGTCATATTGAG | 7011 |
rs779656923 | snp | A/G | 1.65089e-05 | 0.00287301 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395560 | AAGAAACCTCCGCCT[A/G]GGACGGTTCTTTTCA | 7011 |
rs779664603 | snp | C/T | 0.000342489 | 0.0130816 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382339 | AGTGGCAGGCAGGGT[C/T]CGGAGTCTCTCAGAC | 7011 |
rs779673398 | snp | A/C | 1.65004e-05 | 0.00287227 | intron-variant | TEP1 | GRCh38.p7 | 14:20378934 | CCTGGGGCTTCCAAA[A/C]AATGGGGAAGGCCCT | 7011 |
rs779703063 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376761 | GGAGGTTAGAGGTCC[C/T]AGAATGAAGGTGAAG | 7011 |
rs779704233 | in-del | -/CCACCT | 0.000123508 | 0.0078574 | intron-variant | TEP1 | GRCh38.p7 | 14:20377783 | AAGGGCTTAAGGATA[-/CCACCT]CCACCACGCGGTCCT | 7011 |
rs779717480 | snp | C/T | 1.7263e-05 | 0.00293789 | intron-variant | TEP1 | GRCh38.p7 | 14:20381078 | AATTCATTAGGGATA[C/T]GAAGGGGCTGGTGAG | 7011 |
rs779717610 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376721 | AGCAAAGTCTCCCAC[A/G]GGGCAGAAACTCAAA | 7011 |
rs779733791 | snp | C/G | | | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395482 | CAGCTTCTCCCTCTT[C/G]AGCTGCTCATACAAC | 7011 |
rs779737851 | snp | C/G | 1.68156e-05 | 0.00289957 | intron-variant | TEP1 | GRCh38.p7 | 14:20376082 | CTATGGGACCCCAGG[C/G]TTGCATCCTTCTGCA | 7011 |
rs779764984 | snp | C/T | 1.95368e-05 | 0.00312538 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383839 | AGACCCTGGTCAGGA[C/T]GAGCCCCAGAAAAGT | 7011 |
rs779780520 | snp | A/G | 1.67778e-05 | 0.00289631 | intron-variant | TEP1 | GRCh38.p7 | 14:20389783 | AGAGAAGGGATGCTA[A/G]ACAGCCCAGGACATT | 7011 |
rs779790167 | snp | C/T | 0.000329424 | 0.0128298 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407997 | TCAGAGAGCAGGCAA[C/T]TGCTGTTGTTCACAC | 7011 |
rs779791899 | in-del | -/ACA | 0.0205914 | 0.0993563 | intron-variant | TEP1 | GRCh38.p7 | 14:20368784 | CACACACACACACAC[-/ACA]CACACACTTACCAGC | 7011 |
rs779833298 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401870 | TAGAATGAACACAGG[A/G]CAGCTTTGTTTGTAG | 7011 |
rs779861875 | in-del | -/ACCTTCCCC | 1.64823e-05 | 0.0028707 | intron-variant | TEP1 | GRCh38.p7 | 14:20373464 | AAGGTTATTCCGCAT[-/ACCTTCCCC]ACCTCCCTTGACTCT | 7011 |
rs779870289 | snp | C/T | 1.67607e-05 | 0.00289483 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375846 | GGGGTTTTGGGTGTC[C/T]TCACGTCCCAGCAGA | 7011 |
rs779922928 | snp | A/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402546 | GAAATACTTTAAATA[A/T]AGTAACTTATTTAAT | 7011 |
rs779923459 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406604 | GCTCTACTCAACCTT[C/T]AGAGCCTTCGCCCAC | 7011 |
rs779936143 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20397818 | GAGTGTGGTGGTGCA[A/G]TCTCAGCTCACTGCA | 7011 |
rs779940079 | in-del | -/TGGTTTTTTTTTT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410800 | ATTGTTTCTCCTTTG[-/TGGTTTTTTTTTT]TTTTTTTTTTTTTTT | 7011 |
rs779964789 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371491 | TTTTGGATCTTACCA[A/G]ATTTCAGATGGAGCA | 7011 |
rs779977130 | snp | C/G | 1.64781e-05 | 0.00287033 | intron-variant | TEP1 | GRCh38.p7 | 14:20373617 | TGAGTCAGAAGAAGG[C/G]ACGGAGCAGGGGAGA | 7011 |
rs779977845 | snp | A/C | 1.65693e-05 | 0.00287826 | intron-variant | TEP1 | GRCh38.p7 | 14:20401433 | TACTTAGATGGAATG[A/C]ATGCTCAGGGTGCAG | 7011 |
rs779986832 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411758 | ATGGACCTCCCAGGA[C/T]CTCCATAAACTGAAA | 7011 |
rs779998381 | snp | A/G | 1.65551e-05 | 0.00287702 | intron-variant | TEP1 | GRCh38.p7 | 14:20368597 | GGAGGTCAGGGCTAC[A/G]AGCCTCCTTACTAAC | 7011 |
rs779999028 | snp | A/C/T | 6.66182e-05 | 0.00577107 | intron-variant | TEP1 | GRCh38.p7 | 14:20405423 | CTACCAGCTTCACAC[A/C/T]CCCATCCCCTCCTTC | 7011 |
rs780045222 | snp | A/G | 1.66529e-05 | 0.00288551 | intron-variant | TEP1 | GRCh38.p7 | 14:20384969 | GGAGCCCCAGCCTGC[A/G]GGCAACAGACAGTAC | 7011 |
rs780072603 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384469 | CAGCCCGCCAACATA[A/G]GGCCGGCCAGCTGCC | 7011 |
rs780086392 | snp | A/G | 1.64958e-05 | 0.00287187 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403729 | GTGACTGACTGGAGA[A/G]CGGGGTGGCCGGCGG | 7011 |
rs780088247 | snp | A/G | 1.64893e-05 | 0.0028713 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381357 | CAGGAGGGCAACTTC[A/G]GAAGGTGCCTGAGGC | 7011 |
rs780089689 | snp | C/T | 1.64988e-05 | 0.00287213 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406367 | GCATTTGGGTCTCTG[C/T]CCCTTTCTTCTCTTC | 7011 |
rs780121674 | snp | C/G | 3.34225e-05 | 0.0040878 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386528 | TGAGGGGCCGCTCGG[C/G]CCTGCAGTGCTGGCA | 7011 |
rs780147349 | in-del | -/G | 1.64749e-05 | 0.00287005 | intron-variant | TEP1 | GRCh38.p7 | 14:20386213 | GTAGGCATGATGATA[-/G]GGACGTGTGGGAGTC | 7011 |
rs780191407 | snp | C/G | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378809 | CAGTCTGGGCTCAGG[C/G]AGCAGCCAGTGATTT | 7011 |
rs780208669 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398844 | GGATGTAAGTCTTAT[C/T]TGAATTATAGCTGGA | 7011 |
rs780214677 | snp | C/T | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373696 | CACGGGGCTCCATGG[C/T]AGCTGCACAGTGGCT | 7011 |
rs780222751 | snp | A/G | 1.65272e-05 | 0.0028746 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403492 | AAAAGGGAACTGGCT[A/G]TCCTTGAAGAGATCC | 7011 |
rs780234187 | snp | A/C/T | 3.51366e-05 | 0.00419133 | intron-variant | TEP1 | GRCh38.p7 | 14:20381728 | GAAGAAGGAAGAGGC[A/C/T]TGTCAGTGAGCTTCC | 7011 |
rs780285369 | snp | A/C | 3.30017e-05 | 0.00406199 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380010 | CATTGGTGGAGAAGG[A/C]CACAGCAGTAGGGGA | 7011 |
rs780333352 | snp | C/G | | | | | GRCh38.p7 | 14:20415662 | TGAACCCAGGAGGTG[C/G]AGGTTGCAGGGAGCC | 7011 |
rs780360599 | snp | C/T | 6.59631e-05 | 0.00574258 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378453 | GTGGCTATTACCTGC[C/T]CCTCTGGGTGGAAGG | 7011 |
rs780380429 | snp | C/T | 6.66234e-05 | 0.00577124 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371618 | TCCTCCTGTAGAATT[C/T]GGTTCAGGTGAAGAC | 7011 |
rs780383304 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366913 | TCCTAAAAGCATGGG[A/C]CAAGGGCAGGAGGAA | 7011 |
rs780384587 | snp | C/G/T | 4.96293e-05 | 0.00498122 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378060 | CAGTAACTGGCAACC[C/G/T]GCATGCAGGAAAAGC | 7011 |
rs780396884 | snp | C/T | 1.65051e-05 | 0.00287267 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384137 | CTGAAGAAGGCGTGG[C/T]CGGGCAGGACTCGGT | 7011 |
rs780400259 | snp | C/T | 4.94214e-05 | 0.00497074 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391705 | TGCTTCACAGAGAGG[C/T]TCACAGCTGTCTCTA | 7011 |
rs780410695 | snp | A/G | 1.6646e-05 | 0.00288491 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384231 | TCCAGCAGGGCCCCA[A/G]GCTGAGGGTAAATGG | 7011 |
rs780413618 | snp | A/G | 1.67728e-05 | 0.00289588 | intron-variant | TEP1 | GRCh38.p7 | 14:20378564 | AGGAGGAATCAGGAT[A/G]CTGAAGAGAGATGCC | 7011 |
rs780438589 | snp | C/G | 3.29625e-05 | 0.00405958 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390941 | TGAGTGTCTGACCTG[C/G]ACTTGAGCCTGGAGC | 7011 |
rs780458677 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402444 | AGCGTTTTTTCTTAT[A/G]ACGCTAATATATATT | 7011 |
rs780463749 | snp | C/T | 3.49302e-05 | 0.00417898 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383193 | TTGTTAAATGGTGAC[C/T]CCTCCAGCCGCTTCC | 7011 |
rs780468943 | snp | A/G | 3.29516e-05 | 0.00405891 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406253 | TTTCCTGAAGGACAT[A/G]GTCAGTAGGCTCTGG | 7011 |
rs780473874 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20379829 | AGTAAAGTTGCTGAA[G/T]TAATCAGAGTGATAA | 7011 |
rs780510088 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20403628 | CTCTGACTCCCTTTG[A/C]TCCTGGTGTGGGACT | 7011 |
rs780590612 | snp | A/G | 8.40258e-05 | 0.00648119 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377750 | ACCCTGACCACACCT[A/G]AACCTGGGAACCAAG | 7011 |
rs780596939 | snp | A/G | 1.76139e-05 | 0.00296759 | intron-variant | TEP1 | GRCh38.p7 | 14:20382767 | GGCTGCCCGCAGCCA[A/G]CCCTCTGCCCCAGCA | 7011 |
rs780599509 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408498 | GGAGATGAGCACCTG[C/G]CTGCACTGAGCGTGT | 7011 |
rs780619756 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20395298 | TGTTAAAGACAAGGT[A/G]TGCTGTGCAAGAAAC | 7011 |
rs780628550 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401007 | TCCTCCCAGACCGAC[A/G]CTTTGTTCCCCCGTA | 7011 |
rs780658499 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20365975 | AAACTCATCCAGCCT[G/T]TGGGAGACACTGAAA | 7011 |
rs780685515 | snp | A/T | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371258 | TTGGGCTGCAGGACA[A/T]ATATGCCATACTCCT | 7011 |
rs780723830 | snp | C/G | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377682 | GCTGAGTGCCACAGA[C/G]AGGGCAGGAGAGAGA | 7011 |
rs780724004 | in-del | -/ACA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400864 | CCTTATAAATCAAAT[-/ACA]ACAACCAGGCAAAGT | 7011 |
rs780725515 | in-del | -/CTT | 1.6537e-05 | 0.00287545 | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382282 | ATCAGGCCCGTGCTC[-/CTT]CTCCAGTGTGCTCAG | 7011 |
rs780744341 | snp | C/T | 9.88354e-05 | 0.00702908 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408007 | GGCAATTGCTGTTGT[C/T]CACACGGTACAAATC | 7011 |
rs780747097 | snp | C/T | 1.65051e-05 | 0.00287267 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381652 | GGAGGCACAGCCGGG[C/T]ACCAGGGCGCTCCAG | 7011 |
rs780750888 | snp | C/T | 1.65787e-05 | 0.00287907 | intron-variant | TEP1 | GRCh38.p7 | 14:20390631 | GAAATATATCAGTTG[C/T]AGAGGAAAATGTGGG | 7011 |
rs780755757 | snp | A/G | | | splice-donor-variant | TEP1 | GRCh38.p7 | 14:20369342 | CCTTCCTTCAAACTC[A/G]CCTTTCTACGCTGCC | 7011 |
rs780787694 | snp | C/T | 3.29587e-05 | 0.00405934 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390719 | ACAGCAGGTATTTCC[C/T]AAAAGTATTCAGGGA | 7011 |
rs780803704 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386133 | ATGTATCCATAACGG[C/G]AGCCCAGAATCCCCA | 7011 |
rs780819327 | snp | C/T | 3.29527e-05 | 0.00405898 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373354 | TTTCTGAAACAGCAG[C/T]AGCACGGACTGGGCC | 7011 |
rs780821432 | in-del | -/AT | 0.00043176 | 0.0146865 | intron-variant | TEP1 | GRCh38.p7 | 14:20368767 | TGCAGGCGCACGCAC[-/AT]ACACACACACACACA | 7011 |
rs780842658 | snp | A/G | 3.29511e-05 | 0.00405887 | intron-variant | TEP1 | GRCh38.p7 | 14:20386238 | GGAGTCACTGGGGGC[A/G]TGGTATCAGGGAACA | 7011 |
rs780858151 | snp | C/T | 1.64972e-05 | 0.00287199 | intron-variant | TEP1 | GRCh38.p7 | 14:20378964 | TCATTCCAAGACAAA[C/T]GGGGAGGACCCCTTA | 7011 |
rs780860516 | in-del | -/C | 4.9525e-05 | 0.00497595 | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378226 | TAGAGGCTCCGGGTG[-/C]CCCCCAGGTCCTACA | 7011 |
rs780872066 | snp | C/T | 3.46681e-05 | 0.00416327 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374447 | AGCTGCCACAGCGCT[C/T]ACAGCACTCTGATGA | 7011 |
rs780886590 | snp | C/G/T | 3.30903e-05 | 0.00406746 | intron-variant | TEP1 | GRCh38.p7 | 14:20401439 | GATGGAATGCATGCT[C/G/T]AGGGTGCAGCTTCTC | 7011 |
rs780913311 | snp | A/T | 2.0987e-05 | 0.0032393 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386622 | GCCGGATGCTGCGCC[A/T]TCTGGGGATAAGCAG | 7011 |
rs780925018 | snp | A/G | 2.23077e-05 | 0.00333967 | intron-variant | TEP1 | GRCh38.p7 | 14:20374558 | AGTCAGAAGTCAGAG[A/G]AGTGGGATTATCAGC | 7011 |
rs780947643 | snp | C/T | 1.65833e-05 | 0.00287948 | intron-variant | TEP1 | GRCh38.p7 | 14:20403921 | CCACTAGAAGCAAGA[C/T]CCAAACCAACCCTCC | 7011 |
rs780966381 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20404905 | TCCACAAAATACGAA[A/G]CCCAGGCCACCTGAC | 7011 |
rs781004646 | snp | G/T | 4.43174e-05 | 0.00470709 | intron-variant | TEP1 | GRCh38.p7 | 14:20396766 | AGTGAGAAAAACAAA[G/T]GAGAAGGCCAGGCAC | 7011 |
rs781062957 | snp | C/T | 1.64863e-05 | 0.00287104 | intron-variant | TEP1 | GRCh38.p7 | 14:20373236 | CTTTTTTTGTGCCAG[C/T]AACACACCCTGTCTC | 7011 |
rs781091063 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406871 | TATATGTATGTATGA[C/T]TCTTTGCAAAATGCA | 7011 |
rs781117929 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20377525 | ACAAGGGAGTAAGAC[A/G]CTTGGGAAGGGGTAG | 7011 |
rs781121227 | snp | A/C | 1.65176e-05 | 0.00287376 | intron-variant | TEP1 | GRCh38.p7 | 14:20405446 | CCTCCTTCACACCTC[A/C]ATACCTTGAGGATAA | 7011 |
rs781135361 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375623 | CTTAGTTCAATGCCT[A/G]GCACATATCAAGTTT | 7011 |
rs781166168 | snp | C/G | 1.69103e-05 | 0.00290773 | intron-variant | TEP1 | GRCh38.p7 | 14:20369819 | TTAGCCTACCCATAT[C/G]AGTCAACTTGTACCA | 7011 |
rs781170935 | snp | A/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405515 | AAAATGGCAGCCAGG[A/G]TGGGGTCAGATGTAT | 7011 |
rs781176716 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394267 | TAATACTGCATTTTA[C/T]TTAACCCAATATATG | 7011 |
rs781181410 | in-del | -/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20379553 | GTTCAAACAAGAGTG[-/C]CTGCCCTTCTCTATC | 7011 |
rs781198503 | in-del | -/TGG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410800 | ATTGTTTCTCCTTTG[-/TGG]TTTTTTTTTTTTTTT | 7011 |
rs781251572 | snp | C/T | 3.30109e-05 | 0.00406256 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379058 | ATCATCGGAGAGGAA[C/T]AAACAAGCAGAGATT | 7011 |
rs781252115 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20365674 | ACACAAAATACAAGC[C/G]TCCATTTTTATTATT | 7011 |
rs781252389 | snp | C/T | 1.64765e-05 | 0.00287019 | intron-variant | TEP1 | GRCh38.p7 | 14:20384566 | TCCTCTCACCACATC[C/T]CTGTACAGGTGCTCC | 7011 |
rs781261702 | snp | A/C | 0.00033024 | 0.0128457 | intron-variant | TEP1 | GRCh38.p7 | 14:20405447 | CTCCTTCACACCTCA[A/C]TACCTTGAGGATAAA | 7011 |
rs781279917 | snp | A/G | 0.000232999 | 0.010791 | intron-variant | TEP1 | GRCh38.p7 | 14:20391100 | GTTCAGCGGGGGCTG[A/G]TTGGACAAGTGTCAG | 7011 |
rs781309393 | snp | A/G | 0.000181316 | 0.00951973 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383493 | TCACACTCACCCGGG[A/G]AAGCTTCTTTGGGAT | 7011 |
rs781334475 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367423 | AGTTCATGGCTATGA[C/T]TGTGCCACCTCTCAA | 7011 |
rs781384713 | snp | A/C | 1.70571e-05 | 0.00292032 | intron-variant | TEP1 | GRCh38.p7 | 14:20380188 | TTCAGAAAGAGCTGC[A/C]GCTTGCTCTCTGGTG | 7011 |
rs781390846 | in-del | -/CCT | 1.64751e-05 | 0.00287007 | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406315 | CGGCCAGATCCTCCA[-/CCT]CCTCCTCCTCCTCTC | 7011 |
rs781437915 | snp | G/T | 3.3e-05 | 0.00406189 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378161 | CCACCATACTGTCCA[G/T]CCGGCCCACAGCCAC | 7011 |
rs781448990 | snp | C/T | 3.29527e-05 | 0.00405898 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391043 | CACGACGTCCACCTG[C/T]TCCGCCCTCGTGATC | 7011 |
rs781502155 | snp | A/C/G | 1.6681e-05 | 0.00288794 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386549 | AGTGCTGGCAGCACA[A/C/G]ACCTCAGCAGCAGGT | 7011 |
rs781504417 | snp | A/G | 1.65121e-05 | 0.00287329 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377355 | TGGACAGGAGCCAGA[A/G]GGACTGAAGGGAGCA | 7011 |
rs781509293 | snp | A/G | 3.60224e-05 | 0.00424381 | intron-variant | TEP1 | GRCh38.p7 | 14:20407843 | ACAACAGACATGGCT[A/G]GAGTCAAGATGAGTG | 7011 |
rs781541954 | snp | A/G | 1.7612e-05 | 0.00296744 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383283 | AAGGCCAGCACGTGG[A/G]CACCCTGGCTCTGCT | 7011 |
rs781559360 | snp | A/G | 8.53089e-05 | 0.00653048 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383203 | GTGACTCCTCCAGCC[A/G]CTTCCCGTACAGGGC | 7011 |
rs781559597 | snp | C/T | 1.64885e-05 | 0.00287123 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377454 | AGGCCAGGGCGGACA[C/T]TGCCACATCCAGTGC | 7011 |
rs781568466 | snp | C/T | 3.29957e-05 | 0.00406162 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385099 | GAGCGCCCTGAAGGG[C/T]ACTGCTGGGCCTGCG | 7011 |
rs781593127 | snp | A/G | 3.29544e-05 | 0.00405908 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391047 | ACGTCCACCTGCTCC[A/G]CCCTCGTGATCATCA | 7011 |
rs781611059 | snp | A/G | 4.94703e-05 | 0.0049732 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373705 | CCATGGCAGCTGCAC[A/G]GTGGCTAATGGGTCC | 7011 |
rs781625439 | in-del | -/GAA | 1.64906e-05 | 0.00287142 | cds-indel, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395519 | TCCTCATTGCCATCC[-/GAA]GAAGCTGCTGACGGC | 7011 |
rs781627267 | snp | G/T | 1.65173e-05 | 0.00287374 | intron-variant | TEP1 | GRCh38.p7 | 14:20378249 | GTCCTACACAGGGAG[G/T]TAGAAATGGAAACGT | 7011 |
rs781632666 | snp | C/T | 0.000315397 | 0.0125538 | intron-variant | TEP1 | GRCh38.p7 | 14:20403679 | CTTGTCCTGCCCTTC[C/T]TGGAGAAAAGGGGCG | 7011 |
rs781657252 | snp | A/G | 1.65272e-05 | 0.0028746 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406386 | TTTCTTCTCTTCTGA[A/G]TCAAACCAACGACCC | 7011 |
rs781669317 | in-del | -/AC | | | intron-variant | TEP1 | GRCh38.p7 | 14:20407380 | TTTCATTTTTTTGAG[-/AC]ACAGTCTCTCTCTGT | 7011 |
rs781734235 | snp | C/G/T | 5.20461e-05 | 0.00510106 | intron-variant | TEP1 | GRCh38.p7 | 14:20395408 | CCTGTGCCAGGGTAG[C/G/T]CCCGATTGCCCACCC | 7011 |
rs781744268 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376886 | ATACACATATACATA[C/T]AACTTGGAGAAAGGT | 7011 |
rs781754123 | snp | G/T | 1.65236e-05 | 0.00287429 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389281 | GTGTCACATCATTGG[G/T]ATTCAAATCTGTTGA | 7011 |
rs781769497 | snp | A/C | 1.6569e-05 | 0.00287824 | intron-variant | TEP1 | GRCh38.p7 | 14:20389603 | CAGGAAGTATAAGCA[A/C]CCTTACAGGTATTGT | 7011 |
rs781777889 | snp | A/G | 1.65157e-05 | 0.0028736 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380023 | GGCCACAGCAGTAGG[A/G]GATGAGGAAACTGCC | 7011 |
rs796081174 | in-del | -/AAAAAAAAAAAA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400151 | TCAAAAAAAAAAAAA[-/AAAAAAAAAAAA]GAATTATCTACATAT | 7011 |
rs796111815 | in-del | -/CA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368765 | GTGTGCAGGCGCACG[-/CA]CACACACACACACAC | 7011 |
rs796272364 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366770 | AAAATCCCTGTAATA[A/G]CCTTCACTTATCTCC | 7011 |
rs796380094 | multinucleotide-polymorphism | AAA/GAC | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376455 | GAGTGTGTACATAGG[AAA/GAC]GGAACGTGCGGCACT | 7011 |
rs796471859 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398068 | CATAGTTTCTTAATA[A/C]TAATATTTTTAAGGT | 7011 |
rs796520553 | in-del | -/AC | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375095 | AAACTCTGTCTCAAA[-/AC]AAAAAAAAAAAAAAG | 7011 |
rs796575314 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376598 | GTGTCACTTCCACCT[C/T]GTGACCTGTGAGGAC | 7011 |
rs796596338 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20399172 | TGCTGGGATTACAGG[C/T]GTGAGCCATGGTGCC | 7011 |
rs796679866 | in-del | -/AG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20395146 | AATCAGAGCAGAAGC[-/AG]AGAGGACACCAGCAT | 7011 |
rs796682788 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393226 | GGTCTCAAAAAAAAA[A/G]AGAGAAGAAAAAAAA | 7011 |
rs796693997 | in-del | -/GC | | | intron-variant | TEP1 | GRCh38.p7 | 14:20386437 | CCCCTCTTCTCTGCA[-/GC]CCCCACACCTGTTCC | 7011 |
rs796697117 | in-del | -/CA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20413008 | TAGCACATTTAAGCA[-/CA]GTCTGGGTTTCTATT | 7011 |
rs796716363 | in-del | A/GTCT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20369917 | AATCAAGTGCGCAAA[A/GTCT]TTTTTTTTTTTTGAG | 7011 |
rs796738713 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20376576 | CCCTCCTCTTCTCAA[A/G]TGTCCAGTGTCACTT | 7011 |
rs796742695 | in-del | -/A | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411693 | CACAGAAAAAAAAAA[-/A]GTATATACTGTTTTG | 7011 |
rs796763574 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20381219 | GGGAGGGGTAATGGC[A/G]GCGGTGATGGTGGAG | 7011 |
rs796787101 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20389040 | GTAGTCCCAGGTACT[C/T]GGGAGGCGGAGGCAG | 7011 |
rs796803668 | snp | C/T | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373369 | CAGCACGGACTGGGC[C/T]GCTGTGTCCCAGGAG | 7011 |
rs796818687 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394140 | TCTGTGCAGTGGCAT[C/G]ATCATAGCTCACTGC | 7011 |
rs796888903 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20381453 | ATCATTCCCAAGGGC[A/T]GTAGGTGAGCTGGCC | 7011 |
rs796894516 | in-del | -/GT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372412 | TGTGTGTGTGTGTGT[-/GT]ATCTTCATTATAGCA | 7011 |
rs796901832 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20373260 | CTGTCTCTCTCCAAG[A/C]CTCACTCACCTGCTT | 7011 |
rs796954231 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388458 | GTTGAGGGAAATGGA[C/T]GGTATCCAGAGGAAA | 7011 |
rs796982933 | in-del | -/AAAAAAAAAAA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400138 | GCAAAACTCCGTCTC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAG | 7011 |
rs796993957 | in-del | -/CACACA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368765 | GTGTGCAGGCGCACG[-/CACACA]CACACACACACACAC | 7011 |
rs797002045 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20399754 | GGATTAGACTATGGG[C/T]ATTTGCCTCAACCAG | 7011 |