SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs376900 | snp | A/G | 0.495671 | 0.0463237 | intron-variant | CASS4 | GRCh38.p7 | 20:56451479 | AGGGGGATGCATAGG[A/G]GTTTGGTGGATGGAA | 57091 |
rs386274 | snp | A/C | 0.432797 | 0.170544 | intron-variant | CASS4 | GRCh38.p7 | 20:56455025 | AAATAGGACTGACTC[A/C]GTTCCTCTTTGACAT | 57091 |
rs401897 | snp | C/T | 0.408359 | 0.193449 | intron-variant | CASS4 | GRCh38.p7 | 20:56454702 | AAACCTATCTTGGAA[C/T]AAAGGTTAGATGAAA | 57091 |
rs442481 | snp | A/G | 0.496105 | 0.0439572 | intron-variant | CASS4 | GRCh38.p7 | 20:56451476 | GTCAGGGGGATGCAT[A/G]GGGGTTTGGTGGATG | 57091 |
rs718022 | snp | A/G | 0.114036 | 0.209795 | intron-variant | CASS4 | GRCh38.p7 | 20:56428409 | TGAGTCCTGCATTGG[A/G]CAGGAACACCCAGGC | 57091 |
rs735780 | snp | A/G | 0.33533 | 0.234987 | intron-variant | CASS4 | GRCh38.p7 | 20:56434091 | GGTAATGCACAGGGT[A/G]GATTAGGGTACAAGG | 57091 |
rs911159 | snp | A/G | 0.245005 | 0.24995 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56437262 | TCTGGAGCAACACGT[A/G]CCAGAAAGCGAGGGT | 57091 |
rs911163 | snp | A/T | 0.499673 | 0.0127754 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410057 | CCTAGAAAAAACAAC[A/T]TGTGAATTATAGCAT | 57091 |
rs927172 | snp | A/G | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56436376 | TATATATATATATGT[A/G]TATATATATATATAG | 57091 |
rs927173 | snp | C/G | 0.326506 | 0.238006 | intron-variant | CASS4 | GRCh38.p7 | 20:56439671 | TGGGTGACTGACCGG[C/G]ACCCTGTCTTAAAAA | 57091 |
rs927174 | snp | A/C | 0.0685596 | 0.171987 | intron-variant | CASS4 | GRCh38.p7 | 20:56440110 | GCTACAAGACATAGA[A/C]CCAGACAGTTGTTAC | 57091 |
rs1321458 | snp | C/T | 0.477041 | 0.104654 | intron-variant | CASS4 | GRCh38.p7 | 20:56440000 | TGGTGTGGAGAAGGC[C/T]TGAATGGTGAGTAGC | 57091 |
rs1884910 | snp | C/G | 0.499703 | 0.0121769 | intron-variant | CASS4 | GRCh38.p7 | 20:56451685 | AGGCTCAAAAGAATC[C/G]TGAAGGACCTTGAGT | 57091 |
rs1923117 | snp | A/G | 0.251296 | 0.249997 | intron-variant | CASS4 | GRCh38.p7 | 20:56457537 | ATATTTTAATATTAA[A/G]GCAAAAAATAAAATA | 57091 |
rs2024964 | snp | G/T | 0.293551 | 0.246177 | intron-variant | CASS4 | GRCh38.p7 | 20:56454195 | GTCttttgttttttt[G/T]ttgttgttgttcttg | 57091 |
rs2064860 | snp | G/T | 0.490782 | 0.0672626 | intron-variant | CASS4 | GRCh38.p7 | 20:56435906 | aaaattagctgggca[G/T]agtagcgcatgcctg | 57091 |
rs2064861 | snp | A/C | 0.479502 | 0.0991411 | intron-variant | CASS4 | GRCh38.p7 | 20:56432903 | GGGAAGATTTCTGTG[A/C]CGCCCCTGCCCACAC | 57091 |
rs2064862 | snp | C/G | 0.488786 | 0.0740357 | intron-variant | CASS4 | GRCh38.p7 | 20:56432901 | GAAGATTTCTGTGAC[C/G]CCCCTGCCCACACTT | 57091 |
rs2145282 | snp | A/G | | | missense | CASS4 | GRCh38.p7 | 20:56437266 | GAGCAACACGTGCCA[A/G]AAAGCGAGGGTTGGT | 57091 |
rs2426624 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411799 | TATTCATTAGGTACC[A/G]TGAGCAAAGACCAGG | 57091 |
rs2426625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421038 | AGCACCTCTAAAAAT[G/T]ACCATAGAAAGATGG | 57091 |
rs2426626 | snp | G/T | 0.0535932 | 0.154675 | intron-variant | CASS4 | GRCh38.p7 | 20:56421135 | GCTTTGAATTCTTCC[G/T]GGTCAATCAAATGGA | 57091 |
rs2426627 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | CASS4 | GRCh38.p7 | 20:56448877 | Acatcatcactggcc[A/G]tcagagaaatgcaaa | 57091 |
rs2426628 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | CASS4 | GRCh38.p7 | 20:56451641 | TGGCAGACCAGGTGG[A/G]GTCAGCGTGGTGGAA | 57091 |
rs2870737 | snp | A/G | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56436362 | TGTGTGTGTGTGTGT[A/G]TATATATATATGTAT | 57091 |
rs2870738 | snp | A/G | 0.480046 | 0.0983462 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56453111 | ATTAAAGAAAAATAG[A/G]GCAAATATCTGTGGA | 57091 |
rs2870739 | snp | A/T | 0.498525 | 0.0271165 | intron-variant | CASS4 | GRCh38.p7 | 20:56457447 | GTAGGATTTGGGAGA[A/T]GTTGGTTCCATTTTC | 57091 |
rs2870740 | snp | A/G | 0.498158 | 0.0302955 | intron-variant | CASS4 | GRCh38.p7 | 20:56457607 | TCTGGAAATGTTGAG[A/G]GTTCTGATATATCTC | 57091 |
rs2870741 | snp | A/G | 0.498182 | 0.0300969 | intron-variant | CASS4 | GRCh38.p7 | 20:56457614 | ATGTTGAGAGTTCTG[A/G]TATATCTCTGATACT | 57091 |
rs3044223 | snp | A/G | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56436374 | TGTATATATATATAT[A/G]TATATATATATATAT | 57091 |
rs3219626 | in-del | -/ACAC | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56416529 | CACACACACACACAC[-/ACAC]GGAAGTAAACAGAAT | 57091 |
rs3746621 | snp | A/G | 0.000166937 | 0.00913457 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56437364 | CGCTGCAGACAGGCC[A/G]TGCCCCCCATTCCTG | 57091 |
rs3746622 | snp | A/G | 9.93888e-05 | 0.00704872 | missense | CASS4 | GRCh38.p7 | 20:56445966 | TCCCAGGTGTATGAC[A/G]TGCCTACCCAGCACC | 57091 |
rs3746623 | snp | C/G | 0.493842 | 0.0551477 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458420 | TGAACACTGCCGGCT[C/G]TACTTTGGGGCGCTC | 57091 |
rs3746624 | snp | C/T | 0.474213 | 0.110582 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458579 | GAGGGACGTGCGCAA[C/T]GAGATCCTCCGTGGC | 57091 |
rs3746625 | snp | C/T | 0.493702 | 0.055762 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458591 | CAACGAGATCCTCCG[C/T]GGCAGCAGTCACCTC | 57091 |
rs3746626 | snp | A/G | 0.494374 | 0.0527379 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458657 | GAATGCCGTGCTCAC[A/G]TACCCCAGCCCTGCC | 57091 |
rs3761206 | snp | A/G | 0.179744 | 0.239925 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411164 | AATGCTGTCTGACAA[A/G]AAGATAGCGGTAAGC | 57091 |
rs3761207 | snp | A/G | 0.408017 | 0.193729 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411319 | TGAGAGGCTGAGGTG[A/G]GTGGATCACTTGAGG | 57091 |
rs3787390 | snp | A/G | 0.498832 | 0.0241331 | intron-variant | CASS4 | GRCh38.p7 | 20:56440292 | GCTGACTCGGAGCAG[A/G]GCTTTGCTGAGGTTT | 57091 |
rs3787393 | snp | C/T | 0.465788 | 0.126237 | intron-variant | CASS4 | GRCh38.p7 | 20:56455978 | tgcatggctgggccc[C/T]gctctcagaattttt | 57091 |
rs3838042 | in-del | -/C | 0.495708 | 0.0461266 | intron-variant | CASS4 | GRCh38.p7 | 20:56451507 | GAAAAGAAAGGGTTG[-/C]CAAGGGCATTTAGAG | 57091 |
rs3970972 | snp | A/G | 0.486984 | 0.079614 | intron-variant | CASS4 | GRCh38.p7 | 20:56436360 | tgtgtgtgtgtgtgt[A/G]tatatatatatatgt | 57091 |
rs4811694 | snp | A/G | 0.408359 | 0.193449 | intron-variant | CASS4 | GRCh38.p7 | 20:56454332 | AGGAGATAATTTGCT[A/G]CTTTCAGCCCCGACC | 57091 |
rs4811695 | snp | A/T | 0.498503 | 0.0273153 | intron-variant | CASS4 | GRCh38.p7 | 20:56457805 | AGATCATTTGAGATC[A/T]GGGGTTCAAAACCAA | 57091 |
rs4811696 | snp | C/T | 0.498459 | 0.0277128 | intron-variant | CASS4 | GRCh38.p7 | 20:56457996 | CTCCAGCCTGGAAGA[C/T]AAAGGAAAACTCTGT | 57091 |
rs4811697 | snp | A/C | 0.498568 | 0.0267188 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458800 | AGCTTCACACCCACA[A/C]CTTGTGCAACTCTGC | 57091 |
rs5842113 | in-del | -/C | 0.498927 | 0.0231381 | intron-variant | CASS4 | GRCh38.p7 | 20:56435314 | GCTTTATTTATGAAA[-/C]GTATGAACAAAGGTT | 57091 |
rs6014721 | snp | A/T | 0.0134968 | 0.0810323 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410742 | gactccgtctcaaaa[A/T]aaataaataaataaa | 57091 |
rs6014722 | snp | A/T | 0.149665 | 0.228982 | intron-variant | CASS4 | GRCh38.p7 | 20:56414777 | tggtgaaaccccatc[A/T]ctagtaaaaatacaa | 57091 |
rs6014723 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | CASS4 | GRCh38.p7 | 20:56418509 | gttttctagatcact[C/G]aggctgctgtgcaac | 57091 |
rs6014724 | snp | A/G | 0.271162 | 0.249103 | intron-variant | CASS4 | GRCh38.p7 | 20:56423488 | ATATTTTTGTTTAGA[A/G]AGTTATATTCTATTC | 57091 |
rs6014726 | snp | C/T | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56427738 | GATATTTATAGTATA[C/T]GCAGTTTTTAAAATG | 57091 |
rs6014727 | snp | A/C | 0.467946 | 0.122472 | intron-variant | CASS4 | GRCh38.p7 | 20:56434127 | TGCAGTCTCATTCAC[A/C]GTGGGTGGAGGTGTG | 57091 |
rs6014728 | snp | C/T | 0.275999 | 0.248644 | intron-variant | CASS4 | GRCh38.p7 | 20:56436752 | TTTAGCCCGGGGTGG[C/T]GGCACGCATGTGTAG | 57091 |
rs6014729 | snp | A/G | 0.256619 | 0.249912 | intron-variant | CASS4 | GRCh38.p7 | 20:56436758 | CCGGGGTGGCGGCAC[A/G]CATGTGTAGTCCCAG | 57091 |
rs6014730 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | CASS4 | GRCh38.p7 | 20:56438160 | AGCATAGTAGCACAC[A/G]TGTGTAGTCCCAACT | 57091 |
rs6014731 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CASS4 | GRCh38.p7 | 20:56440285 | CTGAGCAGCTGACTC[A/G]GAGCAGAGCTTTGCT | 57091 |
rs6014732 | snp | C/G | 0.136847 | 0.222927 | intron-variant | CASS4 | GRCh38.p7 | 20:56440696 | AGTTTACTATTGAAA[C/G]TTAACTTTGAAAAAT | 57091 |
rs6014733 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | CASS4 | GRCh38.p7 | 20:56442087 | ACTGTTTTCCCATGG[C/T]AAATTCACAGGCTTG | 57091 |
rs6014734 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CASS4 | GRCh38.p7 | 20:56456128 | TTCTCAGTGGAGGCC[C/T]GGGGCACCGTTGGCC | 57091 |
rs6024864 | snp | A/G | 0.486464 | 0.0811471 | intron-variant | CASS4 | GRCh38.p7 | 20:56413446 | GGGAGGCCAAGGCAG[A/G]TGGATCACTTGAGGC | 57091 |
rs6024868 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | CASS4 | GRCh38.p7 | 20:56419466 | CCCCCACACCACCCC[C/T]gctcaggctggagta | 57091 |
rs6024870 | snp | A/G | 0.103794 | 0.20279 | intron-variant | CASS4 | GRCh38.p7 | 20:56422512 | ATATTAAAGCATGTC[A/G]ATCTGGGTAACACCC | 57091 |
rs6024871 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | CASS4 | GRCh38.p7 | 20:56422636 | CCTCCTCAAAGCCCC[A/G]TTAGTAGGCAGTGCC | 57091 |
rs6024875 | snp | A/G | 0.303938 | 0.244112 | intron-variant | CASS4 | GRCh38.p7 | 20:56433036 | TCATTCATTAATTCA[A/G]CAAGTAGCTAAAGAT | 57091 |
rs6024877 | snp | C/T | 0.409552 | 0.192466 | intron-variant | CASS4 | GRCh38.p7 | 20:56438952 | AGACTGAGAAGAACA[C/T]GCTCCAGGCATAGTT | 57091 |
rs6024878 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CASS4 | GRCh38.p7 | 20:56440549 | ATGCCACTCAATACA[A/G]TGACAGGCTCCTACA | 57091 |
rs6024879 | snp | C/T | 0.471863 | 0.115225 | intron-variant | CASS4 | GRCh38.p7 | 20:56442504 | CTACAGATGCTACGT[C/T]ACAGCTCTGTAACTT | 57091 |
rs6024880 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | CASS4 | GRCh38.p7 | 20:56444435 | CCTCTCCTCCAGGCC[C/T]TGTCTTGCTTACCAG | 57091 |
rs6024881 | snp | G/T | 0.144296 | 0.226554 | intron-variant | CASS4 | GRCh38.p7 | 20:56445633 | tgggcccaagaatct[G/T]catgttaacctgctt | 57091 |
rs6024882 | snp | A/G | 0.481396 | 0.0946345 | intron-variant | CASS4 | GRCh38.p7 | 20:56449108 | gccatcccattactg[A/G]gtatatacccaaagg | 57091 |
rs6024883 | snp | G/T | 0.132751 | 0.2208 | intron-variant | CASS4 | GRCh38.p7 | 20:56450321 | gagccaccacgcccg[G/T]ctGAGAAGTCTCTTT | 57091 |
rs6024884 | snp | C/G | 0.482425 | 0.0951571 | intron-variant | CASS4 | GRCh38.p7 | 20:56450456 | AGATTTCTACCATTA[C/G]AGCATCATGACCAAA | 57091 |
rs6024885 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CASS4 | GRCh38.p7 | 20:56451606 | AAACAGCTTGGGTGG[C/T]TGGACCTGTAAGCAG | 57091 |
rs6024887 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CASS4 | GRCh38.p7 | 20:56453287 | AAGTAAAATTCTTGA[C/T]GAAATCTTATTAACA | 57091 |
rs6024888 | snp | A/G | 0.451483 | 0.148002 | intron-variant | CASS4 | GRCh38.p7 | 20:56454981 | TGTAGGGGCTCTGCA[A/G]GGTTGTTGTGGGTGG | 57091 |
rs6024889 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CASS4 | GRCh38.p7 | 20:56456178 | ATTGCGTGGTGAACC[A/G]TTCAGCATCCCAGAA | 57091 |
rs6024890 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CASS4 | GRCh38.p7 | 20:56456616 | ctgacctcaagtgac[C/G]ctcctgcctcagcct | 57091 |
rs6064392 | snp | G/T | 0.110872 | 0.20771 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409712 | TAGAGTCCTTCTGAC[G/T]TAGTTCCCTTGAACT | 57091 |
rs6069737 | snp | C/T | 0.104859 | 0.203554 | intron-variant | CASS4 | GRCh38.p7 | 20:56420643 | caagcagtcctcctg[C/T]ctcagcctcctaaag | 57091 |
rs6069740 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | CASS4 | GRCh38.p7 | 20:56429946 | CACTTACAAGAGATG[A/G]AAACCCTGTatttat | 57091 |
rs6069746 | snp | C/T | 0.32627 | 0.238082 | intron-variant | CASS4 | GRCh38.p7 | 20:56440475 | AAGACCACTTCACAA[C/T]CAGTTAAGTTTTCTG | 57091 |
rs6069749 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | CASS4 | GRCh38.p7 | 20:56446519 | CTTAACATTGATTAT[C/T]TCTGGGGGAAGAAAT | 57091 |
rs6069751 | snp | C/T | 0.498908 | 0.0233371 | intron-variant | CASS4 | GRCh38.p7 | 20:56449391 | gcatgttctcactca[C/T]aggtgggaaatgaac | 57091 |
rs6069753 | snp | A/G | 0.444314 | 0.157297 | intron-variant | CASS4 | GRCh38.p7 | 20:56450706 | GAGGTGCTAAGGTGC[A/G]GTGTTATGAACACAC | 57091 |
rs6069754 | snp | A/C/T | 1.65252e-05 | 0.00287443 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453032 | CTCCCCAAAGAGAAA[A/C/T]TGAATCACACCAAAA | 57091 |
rs6069755 | snp | A/C/T | 4.97302e-05 | 0.00498624 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453062 | AGAGTACCCCTTCCA[A/C/T]TAAGCAAAGGGAAGA | 57091 |
rs6092314 | snp | C/G | 0.138586 | 0.226022 | intron-variant | CASS4 | GRCh38.p7 | 20:56440769 | CATCAACCATTTGAG[C/G]CCTTGCTTGTGCAGG | 57091 |
rs6092315 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CASS4 | GRCh38.p7 | 20:56442455 | TCTGTGGCTGACGCT[A/G]TTCTTTCTGATGAAC | 57091 |
rs6092316 | snp | A/C | 0.465683 | 0.126415 | intron-variant | CASS4 | GRCh38.p7 | 20:56450284 | CTGCCTCAGCCTCCC[A/C]AAGTGTTGGGATTAC | 57091 |
rs6099133 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410247 | gaccttgggcaagtt[A/T]atccatccttcCTTT | 57091 |
rs6099136 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410782 | tatggtacctgaatt[A/G]tatcttaatataata | 57091 |
rs6099137 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410912 | TTATCTGCTATCGCC[G/T]GCAGCATGCCAATTA | 57091 |
rs6099138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421435 | ggtgtggtagtccac[A/G]cctgtaatcccagca | 57091 |
rs6099143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56432275 | AAAGCTTTCAGATTA[C/T]TGTTTTTTACTGAAC | 57091 |
rs6099144 | snp | A/G | 0.14665 | 0.227637 | intron-variant | CASS4 | GRCh38.p7 | 20:56433272 | agtgacatttaagat[A/G]agcctgaaaggatgt | 57091 |
rs6099145 | snp | A/T | 0.493013 | 0.058691 | intron-variant | CASS4 | GRCh38.p7 | 20:56434573 | TCCCAAGTAGCTGGG[A/T]CTACAGGTGCACGCC | 57091 |
rs6099146 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | CASS4 | GRCh38.p7 | 20:56434798 | AAAATTGTGTGTTTC[A/G]TATTATGCCATTAGA | 57091 |
rs6099147 | snp | A/C | 0.104504 | 0.2033 | intron-variant | CASS4 | GRCh38.p7 | 20:56436542 | ttacagatgaggaaa[A/C]tgaggctctaatagg | 57091 |
rs6099148 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | CASS4 | GRCh38.p7 | 20:56439003 | GTTAAAGAGAAAGGG[A/G]GCAGTAAGCTGGGGC | 57091 |
rs6099149 | snp | C/T | 0.103794 | 0.20279 | intron-variant | CASS4 | GRCh38.p7 | 20:56442399 | GACTTCCATCACCCC[C/T]CAAAACACAGCCCTT | 57091 |
rs6099150 | snp | G/T | 0.137867 | 0.223442 | intron-variant | CASS4 | GRCh38.p7 | 20:56449758 | TATCAAATGAGTCTC[G/T]CATACCCTGTTTTTA | 57091 |
rs6099151 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CASS4 | GRCh38.p7 | 20:56455572 | TTTGTTCAACATTAA[A/G]TAGGCCTTAGACTag | 57091 |
rs6123590 | snp | C/T | 0.197393 | 0.244402 | intron-variant | CASS4 | GRCh38.p7 | 20:56414029 | CCCTAAACTTCATTA[C/T]GTGTCTCCTAAGAAC | 57091 |
rs6123591 | snp | C/G | 0.221141 | 0.248329 | intron-variant | CASS4 | GRCh38.p7 | 20:56437858 | GGAATGCTTAGCTGA[C/G]CTGTGTGGGAAGGCA | 57091 |
rs6123592 | snp | C/G | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56442591 | tctgtcacttcccca[C/G]tagggtaaccactat | 57091 |
rs6123594 | snp | C/T | 0.470327 | 0.118136 | intron-variant | CASS4 | GRCh38.p7 | 20:56456683 | CCCAGCTCCCTTTTT[C/T]ATTTTATTTTTTTGA | 57091 |
rs6127743 | snp | A/G | 0.18134 | 0.240387 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409731 | TTCCCTTGAACTCCA[A/G]CTGTTTCAGCCTTCA | 57091 |
rs6127744 | snp | G/T | 0.356383 | 0.226236 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411218 | TAGAACTTGAGCCTG[G/T]CTTGGAAGAATGGGC | 57091 |
rs6127745 | snp | C/G | 0.187685 | 0.242109 | intron-variant | CASS4 | GRCh38.p7 | 20:56412967 | TTTTCATGTTAACTT[C/G]TGCATTATGTGAGCA | 57091 |
rs6127748 | snp | G/T | 0.491263 | 0.0655142 | intron-variant | CASS4 | GRCh38.p7 | 20:56421547 | AAAAAATTTTTAAAA[G/T]TAGCTGGGTTTGGTG | 57091 |
rs6127750 | snp | C/T | 0.207559 | 0.246371 | intron-variant | CASS4 | GRCh38.p7 | 20:56427372 | AGGGGATTTTTCTTA[C/T]GCTCTTGGAAACTTT | 57091 |
rs6127751 | snp | C/T | 0.375399 | 0.216275 | intron-variant | CASS4 | GRCh38.p7 | 20:56431832 | TCGGTTTTTAAAGAT[C/T]GCTTTAAATGTATTT | 57091 |
rs6127753 | snp | A/G | 0.314544 | 0.241524 | intron-variant | CASS4 | GRCh38.p7 | 20:56438981 | TTACCCCAAGGAAGG[A/G]GAACTGGTTAAAGAG | 57091 |
rs6127754 | snp | A/G | 0.455383 | 0.142541 | intron-variant | CASS4 | GRCh38.p7 | 20:56447939 | CGAGGTCAGGAGGTG[A/G]AGACCACCCTGGCTA | 57091 |
rs6127755 | snp | A/G | 0.459801 | 0.135955 | intron-variant | CASS4 | GRCh38.p7 | 20:56453688 | GAGGCAGGAGTTTGA[A/G]ACCAGGCTGGGCAAC | 57091 |
rs7264979 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56442675 | TAATTTAAAAAAAAA[A/C]CCCACCACATCAAGA | 57091 |
rs7266908 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | CASS4 | GRCh38.p7 | 20:56443476 | tccgtctccaaaaaa[A/C]aaaagaaGCTTGGAT | 57091 |
rs7272702 | snp | G/T | 0.0199015 | 0.097748 | missense | CASS4 | GRCh38.p7 | 20:56458726 | GCAACACACGCGGCA[G/T]TTCAGAGGGACACTG | 57091 |
rs7273621 | snp | A/G | 0.046775 | 0.145601 | intron-variant | CASS4 | GRCh38.p7 | 20:56446936 | CTTTTggccaggtgc[A/G]gcagctcacacctat | 57091 |
rs7274581 | snp | C/T | 0.170408 | 0.236992 | intron-variant | CASS4 | GRCh38.p7 | 20:56443204 | CTTGGATTTCTggcc[C/T]ggcgcggtggctcac | 57091 |
rs7347577 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440577 | ACAAGGTACTTAGTA[A/G]ATACCTGTTGCATGA | 57091 |
rs7348371 | snp | C/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411172 | CTGACAAGAAGATAG[C/G]GGTAAGCTATCCCCC | 57091 |
rs8117604 | snp | C/T | 0.271972 | 0.249033 | intron-variant | CASS4 | GRCh38.p7 | 20:56419720 | acaggcgtgagccac[C/T]gtgcccggctAGGCT | 57091 |
rs8117984 | snp | C/G | 0.275999 | 0.248644 | intron-variant | CASS4 | GRCh38.p7 | 20:56437098 | TTTCTAAGAGAGTGG[C/G]ATTGGAGTAGCAGTC | 57091 |
rs8123563 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | CASS4 | GRCh38.p7 | 20:56454393 | AGGAGCTTTAACATG[C/T]TCTAGAAATTTGGAT | 57091 |
rs11086544 | in-del | -/A/AA | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56455145 | TTTAAAAAAAAAAAA[-/A/AA]GTCAAAGATGTTATC | 57091 |
rs11086545 | in-del | -/A | 0.498503 | 0.0273153 | intron-variant | CASS4 | GRCh38.p7 | 20:56457772 | TAATCCCAGCACTTT[-/A]AGGAGGCTGAGGTGG | 57091 |
rs11355939 | in-del | -/A | 0.375 | 0.216506 | intron-variant | CASS4 | GRCh38.p7 | 20:56458036 | AAAAAAAAAAAAAAA[-/A]GTTATAAATATAGTC | 57091 |
rs11374380 | in-del | -/A | 0.19459 | 0.243782 | intron-variant | CASS4 | GRCh38.p7 | 20:56419538 | TTAAGTGATCCTCCC[-/A]ACCTCAGCCTCCCAA | 57091 |
rs11383849 | in-del | -/A/AA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455144 | TCCTTTTTTAAAAAA[-/A/AA]AAAAAAGTCAAAGAT | 57091 |
rs11467181 | in-del | -/AAAAAAAAAAAAAAAAA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443480 | CTCCAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAA]GAAGCTTGGATTTCA | 57091 |
rs11470665 | in-del | -/AA | 0.484491 | 0.0866827 | intron-variant | CASS4 | GRCh38.p7 | 20:56448142 | GTGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 57091 |
rs11472394 | in-del | -/A/AA | 0.499053 | 0.0217445 | intron-variant | CASS4 | GRCh38.p7 | 20:56455133 | TGTTCTTCCTTTTTT[-/A/AA]AAAAAAAAAAAAGTC | 57091 |
rs11473486 | in-del | -/AG | 0.0995161 | 0.199636 | intron-variant | CASS4 | GRCh38.p7 | 20:56438573 | ATATAAACTCAAAAA[-/AG]AGAGGCAGGGCGCAA | 57091 |
rs11475169 | in-del | -/A | 0.449726 | 0.150364 | intron-variant | CASS4 | GRCh38.p7 | 20:56438289 | TGAGAACCTGTTTTC[-/A]AAAAAAAAAAAAAGT | 57091 |
rs11475630 | in-del | -/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56420572 | TTTTTTTTTTTTTTT[-/T]GTAGAGATGAGGGGC | 57091 |
rs11476162 | snp | A/G | 0.230603 | 0.249246 | intron-variant | CASS4 | GRCh38.p7 | 20:56438302 | TCAAAAAAAAAAAAA[A/G]GTATATCCCCTTCAA | 57091 |
rs11476748 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442678 | AATTTAAAAAAAAAA[-/C]CCACCACATCAAGAG | 57091 |
rs11476843 | in-del | -/A | 0.489434 | 0.0719116 | intron-variant | CASS4 | GRCh38.p7 | 20:56442666 | GTGCTGGCCTAATTT[-/A]AAAAAAAAACCCACC | 57091 |
rs11479650 | in-del | -/A | 0.399611 | 0.200291 | intron-variant | CASS4 | GRCh38.p7 | 20:56447857 | GGTGTAAAAGTTATC[-/A]ATGGGCCGGGCGCGG | 57091 |
rs11483269 | in-del | -/T | 0.498589 | 0.02652 | intron-variant | CASS4 | GRCh38.p7 | 20:56438440 | AATGTTTATTAACAG[-/T]TGGATTGGTTATACA | 57091 |
rs11483285 | in-del | -/C | 0.409721 | 0.192325 | intron-variant | CASS4 | GRCh38.p7 | 20:56456089 | ACCTCACTTGGAAAG[-/C]CCCCCGCTTTAGACT | 57091 |
rs11697922 | snp | G/T | 0.224412 | 0.248687 | intron-variant | CASS4 | GRCh38.p7 | 20:56416786 | TCTACAATCTGTACT[G/T]TCTTTTATAAAGACA | 57091 |
rs11698292 | snp | C/T | 0.24134 | 0.24985 | intron-variant | CASS4 | GRCh38.p7 | 20:56422344 | AGAGACCTTTATTGT[C/T]GCATCATTTCAATCC | 57091 |
rs11905250 | snp | G/T | 0.291493 | 0.246533 | intron-variant | CASS4 | GRCh38.p7 | 20:56414270 | CTGATCCAGGTGGTG[G/T]TTGTCAATTCTCAGT | 57091 |
rs11907243 | snp | A/C | 0.115788 | 0.21092 | intron-variant | CASS4 | GRCh38.p7 | 20:56439946 | TGCAGGGAAAGGCCA[A/C]GCTCCCTGAGGCATG | 57091 |
rs12480854 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439190 | ttttgtttttttgag[A/C]ctgggtctcgctctg | 57091 |
rs16979897 | snp | A/T | 0.18134 | 0.240387 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409689 | CAAGAGCATTAAGAT[A/T]ACCTCACTAGAGTCC | 57091 |
rs16979901 | snp | A/G | 0.289942 | 0.246789 | intron-variant | CASS4 | GRCh38.p7 | 20:56413821 | GAAAAATTTCAAACC[A/G]TTGGAAAAATATGGG | 57091 |
rs16979903 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | CASS4 | GRCh38.p7 | 20:56415911 | ATTGTTTTATAGAAC[A/G]AGGCGAAATTTTTTT | 57091 |
rs16979909 | snp | A/G | 0.217551 | 0.247885 | intron-variant | CASS4 | GRCh38.p7 | 20:56431330 | ACATGCATTTCATTC[A/G]TCTTTTGTAACATTA | 57091 |
rs16979923 | snp | A/C | 0.0217159 | 0.101913 | intron-variant | CASS4 | GRCh38.p7 | 20:56437603 | TACGCATACTTCCAC[A/C]TACTAGACATGGGTT | 57091 |
rs16979927 | snp | C/T | 0.109108 | 0.206518 | intron-variant | CASS4 | GRCh38.p7 | 20:56444194 | CAGATAAATCTAGCA[C/T]GTACATTCCCAGTGC | 57091 |
rs16979932 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | CASS4 | GRCh38.p7 | 20:56444783 | ATGTTTCCCAAAGTG[C/T]CTTGAGCAATAACTG | 57091 |
rs16979933 | snp | C/T | 0.146314 | 0.227484 | intron-variant | CASS4 | GRCh38.p7 | 20:56445501 | ATGTAGACGAATAGC[C/T]CAGTATCAGAGTCAC | 57091 |
rs16979934 | snp | C/T | 0.089084 | 0.191327 | intron-variant | CASS4 | GRCh38.p7 | 20:56451723 | GAAATGGGGAGCCAC[C/T]GAAGGAGCGGCGGAG | 57091 |
rs16979936 | snp | A/G | 0.00645658 | 0.05645 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452648 | TAGAAGAATCTGTAA[A/G]AGAATTTCTGGATTT | 57091 |
rs17365060 | snp | A/G | 0.239037 | 0.24976 | intron-variant | CASS4 | GRCh38.p7 | 20:56425893 | AAAGATGCTATACTT[A/G]TAAAAGCATCAATGC | 57091 |
rs17462136 | snp | C/G | 0.106633 | 0.204807 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412160 | TTGTGGTTTCACATA[C/G]CAAATGAGTGACAGT | 57091 |
rs28540576 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440988 | TACTTAAAAAAAAAA[A/T]TTTTTTTTTTTTTTT | 57091 |
rs33961391 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435315 | CTTTATTTATGAAAG[-/C]TATGAACAAAGGTTA | 57091 |
rs34045473 | in-del | -/C | | | upstream-variant-2KB, intron-variant | CASS4 | GRCh38.p7 | 20:56412245 | TTTCTGGTCCTCCCC[-/C]TGCTTCACTGCTTTC | 57091 |
rs34102676 | snp | A/G | 0.00827947 | 0.0638058 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56437340 | TGCAGCGACCTCCGT[A/G]AGGATTTGGAGGCGG | 57091 |
rs34216723 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426890 | GCCAGCTTCTCCCCC[-/C]TTATTTGGTTAGTTA | 57091 |
rs34219740 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431715 | CAGCTAAGCTGCATT[-/T]CAATCTGGACCCTTC | 57091 |
rs34227954 | in-del | -/C | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410890 | GGGGTCATTGTTCCC[-/C]TCCCTGTTATCTGCT | 57091 |
rs34251812 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | CASS4 | GRCh38.p7 | 20:56431873 | ACGATGAAATATACC[A/G]TAATTATTTCATTAT | 57091 |
rs34298978 | in-del | -/T | | | utr-variant-5-prime, intron-variant | CASS4 | GRCh38.p7 | 20:56412259 | CTGCTTCACTGCTTT[-/T]CATTTTACTCTTATC | 57091 |
rs34457258 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56449233 | CCAGTGATAGACTGG[-/C]ATTAAGAAAATGTGG | 57091 |
rs34486590 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415926 | AAGGCGAAATTTTTT[-/T]AAAACACGTGATATT | 57091 |
rs34895786 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414475 | AGCAATGGGGGTATC[-/C]ACTCTGTTGTCCAAG | 57091 |
rs34899200 | snp | A/G | 0.0103657 | 0.0712419 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452453 | TTTGCTGACTCCTCC[A/G]AGGAAGAGCTGGAGG | 57091 |
rs35031530 | snp | A/G | 0.101445 | 0.201076 | missense | CASS4 | GRCh38.p7 | 20:56458364 | TCTGTTGACTCGAAG[A/G]CTGAGGTATAAGAGG | 57091 |
rs35217347 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413699 | AAAAAAAAAAAAAAA[-/A]GTCACTAGTGGAATT | 57091 |
rs35219111 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434990 | TCTTTAATGAACTTT[-/T]ATTACTTTTGTAGAA | 57091 |
rs35324103 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459481 | TGGAGTTGTACCTGA[C/T]TTTATTACCAGTTTT | 57091 |
rs35335198 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443144 | ACACTCACTCAAGGT[-/C]CCCTGGGTGTGGCGG | 57091 |
rs35360819 | snp | C/T | 0.0174225 | 0.0916936 | missense | CASS4 | GRCh38.p7 | 20:56437405 | TAGGTCTCCTCTGAG[C/T]TGGCAGGAGCTTCTT | 57091 |
rs35616116 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434933 | GCAGCACTGCAGGCA[-/A]TTTTAATTTTCTTCT | 57091 |
rs35635359 | in-del | -/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424510 | TTTGGGAGGTCAAGG[-/G]CGGGTGGATCATCTG | 57091 |
rs35742452 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448647 | CTCTACAGAAACCCC[-/C]TTCCAATATCCAACT | 57091 |
rs35758996 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431671 | GTTCTCTGGGAAAAA[-/A]GTCCTTACTTTTACA | 57091 |
rs35814212 | in-del | -/T | 0.44252 | 0.159487 | intron-variant | CASS4 | GRCh38.p7 | 20:56456380 | CTTCTTTTTTTTTTT[-/T]GAGACGAAGTCTTGC | 57091 |
rs35818108 | in-del | -/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56449434 | GGACACAGGGTGGGG[-/G]AACATCACACACCGG | 57091 |
rs35839931 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56422481 | CTTAGCAAGGTTTCC[-/C]ATGAGTAGAGGAAGT | 57091 |
rs35963900 | in-del | -/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440040 | TTGTCTTCAAACAGG[-/G]AAAGTGTTGATTCCT | 57091 |
rs35972653 | in-del | -/TG | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436337 | GGATTGCTATATATA[-/TG]TGTGTGTGTGTGTGT | 57091 |
rs41490147 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | CASS4 | GRCh38.p7 | 20:56422692 | TCCTGATGATTCAGA[C/T]GAAAAAGCCACACAT | 57091 |
rs55688724 | in-del | -/G | 0.0197687 | 0.0974348 | intron-variant | CASS4 | GRCh38.p7 | 20:56435942 | TTTTTATTAGAGACA[-/G]GGTTTCACCATGTTG | 57091 |
rs55708816 | snp | A/G | 0.298398 | 0.245271 | intron-variant | CASS4 | GRCh38.p7 | 20:56415068 | AGGTGGCAATGCCAG[A/G]AATCAACCCCAGGCA | 57091 |
rs55844300 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427143 | AGCCACTGCATTCCA[A/G]CCTGGGCAACATAGC | 57091 |
rs55896430 | snp | A/G | 0.021333 | 0.101051 | intron-variant | CASS4 | GRCh38.p7 | 20:56435535 | CTTTAAAACCTAAAG[A/G]AACAAGTTGCCTTCA | 57091 |
rs56012565 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | CASS4 | GRCh38.p7 | 20:56430168 | TATCCTTGGCTGCTC[A/G]GGTTTAGATGAGCAC | 57091 |
rs56030851 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56458267 | CTTGCAAATCTAGCC[A/T]AAACAGGAAAGGGCA | 57091 |
rs56091263 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412344 | GTTGTCAGATAGCTC[C/T]ATAGAATTCAGTTTC | 57091 |
rs56207457 | in-del | -/GT | 0.485528 | 0.0838238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416529 | ATTCTGTTTACTTCC[-/GT]GTGTGTGTGTGTGTG | 57091 |
rs56704283 | in-del | -/TT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420571 | TTTTTTTTTTTTTTT[-/TT]GTAGAGATGAGGGGC | 57091 |
rs56793091 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CASS4 | GRCh38.p7 | 20:56417764 | GCAGGTGTTTGGCAA[C/T]GGAGGTCATTCCTGA | 57091 |
rs56872912 | in-del | -/C | 0.0420721 | 0.138802 | intron-variant | CASS4 | GRCh38.p7 | 20:56446019 | AGCCTTGTTCAGGGG[-/C]CCCCTCATCACCCAG | 57091 |
rs57076617 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CASS4 | GRCh38.p7 | 20:56448127 | AGCCTGGGAGACAGA[A/G]TGAGACTCTGTCTCA | 57091 |
rs57238494 | snp | A/G | 0.180064 | 0.240019 | intron-variant | CASS4 | GRCh38.p7 | 20:56424957 | ACTTCAGGAGTTGTA[A/G]GAGGTTTTCCAGGAG | 57091 |
rs57375620 | snp | A/C/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409784 | ACCCAGTTTCCTAGA[A/C/T]TAATAGTTCTTGCAA | 57091 |
rs58116150 | snp | A/T | 0.0941369 | 0.195465 | intron-variant | CASS4 | GRCh38.p7 | 20:56444553 | GCATTCCTAGTCCCC[A/T]CCTAGAGACGTTCTA | 57091 |
rs58241683 | in-del | -/GT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436361 | TGTGTGTGTGTGTGT[-/GT]ATATATATATATGTA | 57091 |
rs58426782 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448428 | TCCACAGCACGGCTG[C/T]CACCCTCTCTCTTTT | 57091 |
rs58644568 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410874 | CAAACTGTTCATTGC[A/G]TGGGGTCATTGTTCC | 57091 |
rs58671794 | in-del | -/GT/GTGT/TA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416528 | TGTGTGTGTGTGTGT[-/GT/GTGT/TA]ATGCACACATGCCAT | 57091 |
rs58686963 | snp | C/T | 0.106278 | 0.204558 | intron-variant | CASS4 | GRCh38.p7 | 20:56456115 | AGACTGACAGCACTT[C/T]TCAGTGGAGGCCCGG | 57091 |
rs59314083 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439350 | AAAGTATCAATTTTT[A/T]AAAACAGAGGAAAAA | 57091 |
rs59337131 | in-del | -/AA | | | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411561 | AAAAAAAAAAAAAAA[-/AA]TGCAGACTTATTTTG | 57091 |
rs59400829 | snp | C/T | 0.225597 | 0.248806 | intron-variant | CASS4 | GRCh38.p7 | 20:56429789 | GCTTTCTCAGGTAAA[C/T]GTCCCTAAGCCCTCA | 57091 |
rs59424187 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | CASS4 | GRCh38.p7 | 20:56455185 | ATTTTTATTGGTTTC[C/G]TTCTATTTGTGGTCA | 57091 |
rs59487573 | snp | G/T | 0.0941369 | 0.195465 | intron-variant | CASS4 | GRCh38.p7 | 20:56444548 | TGTGCGCATTCCTAG[G/T]CCCCTCCTAGAGACG | 57091 |
rs59500684 | snp | A/G | 0.148326 | 0.228391 | intron-variant | CASS4 | GRCh38.p7 | 20:56451498 | TGGTGGATGGAAAAG[A/G]AAGGGTTGCCAAGGG | 57091 |
rs59859042 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413168 | ATAGCGAGACCCCAT[C/T]TTAAAAAAAAAAAAA | 57091 |
rs59877333 | snp | C/T | 0.0123036 | 0.0774623 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411964 | GGAAGAAATGCTGAC[C/T]GCTATCAGAAATTTG | 57091 |
rs59896238 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432388 | TTTTTTTTTTTGAGA[A/G]ACAGGGTCTCACTTC | 57091 |
rs59958106 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56433255 | GACCCTTTTTCTAAG[A/G]AAGTGACATTTAAGA | 57091 |
rs60118684 | in-del | -/T | 0.210605 | 0.246877 | intron-variant | CASS4 | GRCh38.p7 | 20:56428943 | CCCCCAGCCCTGACA[-/T]TCTTGAGTTTCTGCA | 57091 |
rs60280958 | snp | C/G | 0.0532157 | 0.154195 | intron-variant | CASS4 | GRCh38.p7 | 20:56420871 | ATTCTCGGTAAGCCC[C/G]CTTTGGGTATCCCAA | 57091 |
rs60742243 | in-del | -/TATATA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436390 | ATATATATATATATA[-/TATATA]GGATATATGTTGGGT | 57091 |
rs60796590 | in-del | -/A | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56447208 | TGAAAAAAAAAAAAA[-/A]TCAAAATCAAAAATT | 57091 |
rs60811492 | snp | C/G | 0.227074 | 0.248947 | intron-variant | CASS4 | GRCh38.p7 | 20:56436283 | GGCACCTGTACATGA[C/G]AGAGAGAGAGATACC | 57091 |
rs60905129 | snp | A/C | 0.0818113 | 0.184966 | intron-variant | CASS4 | GRCh38.p7 | 20:56433432 | AAGTGTGGGAAGAGG[A/C]AAAATCACACAGGGC | 57091 |
rs61440974 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | CASS4 | GRCh38.p7 | 20:56444846 | CCAGGCGCGGTGGCT[C/T]ACGCCTGTAATCCCA | 57091 |
rs61482907 | snp | C/T | 0.2776 | 0.248472 | intron-variant | CASS4 | GRCh38.p7 | 20:56414309 | TAGAACAATCTACTA[C/T]CTTTTTCTCTTTCAT | 57091 |
rs62209418 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CASS4 | GRCh38.p7 | 20:56419307 | CAAACATAACGCCTA[C/T]GAAGTGTTTGTTCAG | 57091 |
rs62209419 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424539 | TGAGGTCAGGAGTTC[C/G]AGACCAGCCTGGCCA | 57091 |
rs62209420 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424551 | TTCGAGACCAGCCTG[A/G]CCAACATGGGGAAAC | 57091 |
rs62209421 | snp | A/G | 0.211212 | 0.246973 | intron-variant | CASS4 | GRCh38.p7 | 20:56429075 | CAGTGTGTCCACCCC[A/G]GCCTAGAGAGGGGAT | 57091 |
rs62209422 | snp | A/C | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56433030 | TCTCTTTCATTCATT[A/C]ATTCAACAAGTAGCT | 57091 |
rs62209423 | snp | G/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56441007 | TTTTTTTTTTTTTTG[G/T]AGGCAGAATCTCGCT | 57091 |
rs62209424 | snp | A/G | 0.426354 | 0.177198 | intron-variant | CASS4 | GRCh38.p7 | 20:56441377 | TGGGAGGCCAAGGCG[A/G]GTGGATCACCTGAGG | 57091 |
rs62209425 | snp | G/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56442299 | TGCATATCTTTAGAT[G/T]AGAACAACTCTTCAT | 57091 |
rs62209456 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56443995 | GCAGTCGTCACTCAA[A/C/T]GAAGGGGGCTGTTTT | 57091 |
rs62209457 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444011 | GAAGGGGGCTGTTTT[A/G]ACATGTGACAGCTGC | 57091 |
rs62209458 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CASS4 | GRCh38.p7 | 20:56451282 | AATGGCTTCTTCTTA[C/T]GACAGACCTCAGGGG | 57091 |
rs67041321 | snp | G/T | 0.319136 | 0.24025 | intron-variant | CASS4 | GRCh38.p7 | 20:56413116 | CTGAGGTGAGAAGAT[G/T]AATTCAGCCCAGAAG | 57091 |
rs72509155 | in-del | -/TCA | 0.2776 | 0.248472 | upstream-variant-2KB, cds-indel | CASS4 | GRCh38.p7 | 20:56411993 | TGGCCTAGTGGCCTC[-/TCA]TCAGGGAAATGAGCT | 57091 |
rs73156368 | snp | C/T | 0.189576 | 0.242588 | intron-variant | CASS4 | GRCh38.p7 | 20:56413016 | AGACTTCATGCCTGT[C/T]ATGAATCAAAAAAGA | 57091 |
rs73156377 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CASS4 | GRCh38.p7 | 20:56418125 | TGAGCATGACAGTGA[G/T]TAAATAGACCCATGG | 57091 |
rs73159591 | snp | A/G | 4.94262e-05 | 0.00497098 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451939 | CCAGGAAAGGCCAGC[A/G]TCAGAAACACGCCTC | 57091 |
rs73285280 | snp | A/G | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | CASS4 | GRCh38.p7 | 20:56412223 | TTGAGACGTGAGTGT[A/G]GCTTGTATTTCTGGT | 57091 |
rs73285288 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CASS4 | GRCh38.p7 | 20:56418699 | ACCGCTGGTCGCCGT[A/G]TCGGGTGGGGAGTGG | 57091 |
rs73285297 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CASS4 | GRCh38.p7 | 20:56432948 | AGACAGAAATAGGAG[C/T]GCTCATCCTGGTGTT | 57091 |
rs73285302 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56434894 | AACACAAAAACCGAA[A/G]GATTAACAGCAGTTA | 57091 |
rs73612601 | snp | A/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410654 | TGAGGCAGGAGAATC[A/T]CTTGAAACCTGGAGG | 57091 |
rs73612602 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441351 | GGCTCACACCTGTAA[G/T]CCCAGCAATTTGGGA | 57091 |
rs73614303 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56457097 | TTTTCCAAATATGCA[A/G]TTCTAATAATGAAGG | 57091 |
rs73913926 | snp | A/G | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56418564 | CAAAAGCTGGTAAAC[A/G]TGGAGACTTCAGTGT | 57091 |
rs73913929 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | CASS4 | GRCh38.p7 | 20:56430836 | AAGAAAAGGTCTGAG[A/G]TGGAAGCAACCTCAG | 57091 |
rs73913931 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | CASS4 | GRCh38.p7 | 20:56432827 | TGTGCAGACTAGTTA[C/T]GCCTTGAGGTTTATC | 57091 |
rs74394902 | snp | C/T | 3.29522e-05 | 0.00405894 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458423 | ACACTGCCGGCTCTA[C/T]TTTGGGGCGCTCTTC | 57091 |
rs74691038 | snp | A/C | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56448143 | TGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 57091 |
rs74753154 | snp | C/T | 0.247053 | 0.249983 | intron-variant | CASS4 | GRCh38.p7 | 20:56440181 | GGAGGAAGCTGGTGG[C/T]GCCTTCTGAAGCAGT | 57091 |
rs74921812 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56430846 | CTGAGGTGGAAGCAA[C/T]CTCAGGGCATTTGAG | 57091 |
rs74932500 | in-del | -/CTAT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56458315 | GATTGAATCTCCTAT[-/CTAT]TTTCTTCCTTCCCTT | 57091 |
rs75067914 | snp | A/G | 0.0244538 | 0.107838 | upstream-variant-2KB, intron-variant | CASS4 | GRCh38.p7 | 20:56412224 | TGAGACGTGAGTGTG[A/G]CTTGTATTTCTGGTC | 57091 |
rs75131704 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56436932 | ATATTAGGACCATCC[A/G]ACCTCGTCTCAGGAT | 57091 |
rs75193011 | snp | A/G | 0.100588 | 0.200439 | intron-variant | CASS4 | GRCh38.p7 | 20:56451196 | TTCTCTGTTTTTATG[A/G]GCTGGGAGTATTAAG | 57091 |
rs75225999 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CASS4 | GRCh38.p7 | 20:56442573 | AGCCTCCAGTGCCTT[C/T]TCTCTGTCACTTCCC | 57091 |
rs75273965 | snp | A/G | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56447208 | GCAAGACTCTGTCTG[A/G]AAAAAAAAAAAATCA | 57091 |
rs75391341 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56433372 | AAGCCCTCAGAAAGG[G/T]TGACACCCTGGAGGC | 57091 |
rs75528071 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | CASS4 | GRCh38.p7 | 20:56446055 | TGCGCCCAGAGTCTG[A/G]GGTTCTTGGGATCAT | 57091 |
rs75637883 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56442825 | CTCCCTAAACCTTTC[A/G]AAACTGTGTTTCTCA | 57091 |
rs75720326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433338 | TTGGGGTAGAGAGAA[C/T]AGCATGATGGAGGGA | 57091 |
rs75890703 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | CASS4 | GRCh38.p7 | 20:56425994 | ACATAAGCTCTACCT[C/T]ATTCTTGTAATGGCT | 57091 |
rs76008201 | snp | C/T | 0.021333 | 0.101051 | intron-variant | CASS4 | GRCh38.p7 | 20:56428112 | TTCCCAAAGAAAGAA[C/T]GATATTCTAGGTTAC | 57091 |
rs76018789 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CASS4 | GRCh38.p7 | 20:56453350 | AGGTCAGTTGATTTG[A/G]ATTTCTTCCGAAAAC | 57091 |
rs76049933 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | CASS4 | GRCh38.p7 | 20:56438086 | TTTGAACTCAGAGTT[C/T]GGGACCAGCCTGGGC | 57091 |
rs76068960 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | CASS4 | GRCh38.p7 | 20:56413089 | ATACCTGTACTCCAG[C/G]TACCGGAGAGGCTGA | 57091 |
rs76074215 | in-del | -/GA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419007 | AGCACACTTGGGGGG[-/GA]AAAAAAAGCTAAGGA | 57091 |
rs76219345 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | CASS4 | GRCh38.p7 | 20:56421226 | ACAATACTGGTGTAT[C/G]TTGATTTGCATTCAA | 57091 |
rs76369311 | snp | A/C | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56448141 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 57091 |
rs76381508 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CASS4 | GRCh38.p7 | 20:56420210 | CAACTGCTTCACCTT[A/G]TCATCAAGAGCAGCT | 57091 |
rs76484485 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | CASS4 | GRCh38.p7 | 20:56432956 | ATAGGAGCGCTCATC[C/T]TGGTGTTTGTGATTT | 57091 |
rs76558241 | snp | C/T | | | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452302 | GAGGTGTCAGAGAAT[C/T]CCGCGGGCCATAATT | 57091 |
rs76611353 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | CASS4 | GRCh38.p7 | 20:56416560 | GTGTGTGTGTGTGTA[A/T]GCACACATGCCATTA | 57091 |
rs76703772 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CASS4 | GRCh38.p7 | 20:56456234 | AGTCCCTAGTCAATG[C/T]GATAACCAAAACTAT | 57091 |
rs76820681 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CASS4 | GRCh38.p7 | 20:56451235 | TCCTGCAAAGGACCC[A/G]GGACAGTGCCTGGCA | 57091 |
rs76842328 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | CASS4 | GRCh38.p7 | 20:56437936 | ACTGCCAGTGACAAA[C/T]GGGAGGGTGGGGTTT | 57091 |
rs77443343 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56422077 | CTTGCCTCCTCCTTC[C/G]GTGGGTTTTTCATGA | 57091 |
rs77523781 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | CASS4 | GRCh38.p7 | 20:56439189 | ATTTTGTTTTTTTGA[G/T]ACTGGGTCTCGCTCT | 57091 |
rs77539228 | snp | A/T | 0.276267 | 0.248616 | intron-variant | CASS4 | GRCh38.p7 | 20:56437104 | AGAGAGTGGGATTGG[A/T]GTAGCAGTCACTGGC | 57091 |
rs77573477 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56430403 | ACATTTCTTCCATTG[C/T]ACCCAGAATCTAACT | 57091 |
rs77584750 | snp | A/G/T | 0.5 | 0 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459523 | ACTGGGGAGTGGGGC[A/G/T]ATTTTGTTTTAATTT | 57091 |
rs77627768 | snp | C/T | 0.00471462 | 0.0483227 | missense | CASS4 | GRCh38.p7 | 20:56445943 | GGGCCTCACTGCCGA[C/T]TCTGCCTTCCCAGGT | 57091 |
rs77689922 | snp | A/G | 0.077417 | 0.180873 | intron-variant | CASS4 | GRCh38.p7 | 20:56445542 | TCCCTAGAGAACATC[A/G]GAATCACCTGGCAAG | 57091 |
rs77696218 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444975 | ATTAGCCTGGCATGG[A/G]GGCATGTGCCTGTAG | 57091 |
rs77703056 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56423002 | GGAGAGAATGCGTTA[A/T]GTAACCAGCCCATCC | 57091 |
rs77723167 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CASS4 | GRCh38.p7 | 20:56451600 | GAAAGTAAACAGCTT[A/G]GGTGGCTGGACCTGT | 57091 |
rs77727026 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411845 | TCCGAGCAGGGTGAA[C/T]GCACAACTGACAGGG | 57091 |
rs77750154 | snp | A/C | 0.277778 | 0.248452 | intron-variant | CASS4 | GRCh38.p7 | 20:56439672 | GGGTGACTGACCGGG[A/C]CCCTGTCTTAAAAAA | 57091 |
rs77988969 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | CASS4 | GRCh38.p7 | 20:56432879 | ATTCTTACCGAAGGT[C/T]ATCCAAAAGTGTGGG | 57091 |
rs78249071 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | CASS4 | GRCh38.p7 | 20:56453372 | TCCGAAAACTTTTGG[C/T]GTTCAAGTTTACCAT | 57091 |
rs78255458 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CASS4 | GRCh38.p7 | 20:56416054 | CTAGAAATTTAGTTT[C/T]CGTGGGTTTTTTTGA | 57091 |
rs78321980 | in-del | -/AA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427191 | AAAAAAAAAAAAAAA[-/AA]CCCTCTGTCACCCTT | 57091 |
rs78381155 | snp | A/C | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56438291 | AGAACCTGTTTTCAA[A/C]AAAAAAAAAAAGTAT | 57091 |
rs78812829 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | CASS4 | GRCh38.p7 | 20:56448576 | AGGCAACCCCCGCTA[C/T]ACCGCACCCCATTTC | 57091 |
rs78897733 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56430939 | CTGATCCTGCCTCGA[A/C]GCCACACTAGGAAGG | 57091 |
rs78902076 | snp | G/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56456391 | TCTTCTTTTTTTTTT[G/T]GAGACGAAGTCTTGC | 57091 |
rs78949129 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | CASS4 | GRCh38.p7 | 20:56417552 | TTCCTCTCTGGGAAC[A/G]AAACTCCATGAGGGA | 57091 |
rs79044968 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CASS4 | GRCh38.p7 | 20:56431872 | TACGATGAAATATAC[C/T]ATAATTATTTCATTA | 57091 |
rs79083916 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CASS4 | GRCh38.p7 | 20:56419288 | ATTTTTTAGGAACCA[C/T]TTCCAAACATAACGC | 57091 |
rs79181856 | snp | C/G | 0.0883596 | 0.190715 | intron-variant | CASS4 | GRCh38.p7 | 20:56432898 | CAAAAGTGTGGGCAG[C/G]GGCGTCACAGAAATC | 57091 |
rs79197736 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | CASS4 | GRCh38.p7 | 20:56428575 | ACAGCCTCCACCACA[C/T]CCAAATGTCTTACGC | 57091 |
rs79282013 | snp | A/G | 0.021333 | 0.101051 | intron-variant | CASS4 | GRCh38.p7 | 20:56451630 | TAAGCAGATGGTGGC[A/G]GACCAGGTGGGGTCA | 57091 |
rs79463340 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | CASS4 | GRCh38.p7 | 20:56451572 | GGCATGAGTCAGTGT[C/T]CTGAGTTCAGGGGAA | 57091 |
rs79489333 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CASS4 | GRCh38.p7 | 20:56421296 | GTAACATCGCTGAGG[A/G]ACAGTTGTTTTTTAA | 57091 |
rs79636199 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56455624 | TCACAATCACCTATG[A/C]TCTTTGTTAAAACTC | 57091 |
rs79693140 | snp | C/G | 0.0566069 | 0.158427 | intron-variant | CASS4 | GRCh38.p7 | 20:56448468 | CAAGCCAGAGTCAGC[C/G]CCCAACCACTGTGAC | 57091 |
rs79737706 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CASS4 | GRCh38.p7 | 20:56417085 | TAAACACGACAAAAT[A/G]TGTTGGCTTGGAAGT | 57091 |
rs79834838 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CASS4 | GRCh38.p7 | 20:56456323 | GGTTAATATTTTCAC[C/T]TAAGATGCTCATAAT | 57091 |
rs79892039 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | CASS4 | GRCh38.p7 | 20:56422509 | AGTATATTAAAGCAT[A/G]TCGATCTGGGTAACA | 57091 |
rs79910377 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CASS4 | GRCh38.p7 | 20:56415647 | AAGGGGTCATGTCAT[A/G]TCAGTGGTCCTTAGC | 57091 |
rs80170602 | snp | A/T | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56434604 | ACCACTCCCAGCTAA[A/T]TTTTTTTTTTTTTTG | 57091 |
rs80181614 | in-del | -/ATTT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440988 | TACTTAAAAAAAAAA[-/ATTT]TTTTTTTTTTTTTTG | 57091 |
rs80263894 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | CASS4 | GRCh38.p7 | 20:56423299 | CATCCATTTCCTACA[A/G]CTCTTTGATTGTGTG | 57091 |
rs111246730 | snp | G/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56439488 | CTAGCCTGGGCAACA[G/T]AGTGAGACCTCATCT | 57091 |
rs111295377 | snp | C/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56433078 | TCCTGGATCATGGGA[C/T]GCAGTCCAGAACAAG | 57091 |
rs111302501 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-5-prime, intron-variant | CASS4 | GRCh38.p7 | 20:56412273 | TTCATTTTACTCTTA[C/T]CGTGCTTTCCAGAAA | 57091 |
rs111416975 | snp | A/G | 0.00557542 | 0.0525036 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459681 | CACCATATTAGCCAG[A/G]CTGGTCTGGAACTCC | 57091 |
rs111451360 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56454329 | TCAAGGAGATAATTT[G/T]CTACTTTCAGCCCCG | 57091 |
rs111472365 | snp | C/T | 8.28823e-05 | 0.00643695 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56445902 | CTTTCTCTCCAAGGC[C/T]ATCCTCACGCTTCCC | 57091 |
rs111490246 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | CASS4 | GRCh38.p7 | 20:56443603 | AAGAGGGAGATCACA[A/G]AGCAGAGGAACCATG | 57091 |
rs111510670 | snp | C/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56438971 | CCAGGCATAGTTACC[C/T]CAAGGAAGGGGAACT | 57091 |
rs111772826 | snp | C/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56428078 | ACTATGGACTGGTGA[C/T]CTCACTGTATGATTT | 57091 |
rs111797066 | in-del | -/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56413467 | ACTTGAGGCCAGGAG[-/T]TTTGAGACCAGCCTG | 57091 |
rs111856018 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | CASS4 | GRCh38.p7 | 20:56445590 | TTCCCGGCCCCCCTC[A/G]ACACCCAGAGACTCC | 57091 |
rs111899912 | snp | A/G | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56429234 | ATGATGAAAGTGTGC[A/G]GGCCAGTTCCCTCTC | 57091 |
rs111905657 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56444284 | CCTCTGCCTGCGTTC[C/T]CCTCCCTCAGCTCTG | 57091 |
rs111975156 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56449862 | GAATAAATATGAATG[A/G]TAAAACAGGAAAATT | 57091 |
rs112103060 | in-del | -/A | 0.21845 | 0.248001 | intron-variant | CASS4 | GRCh38.p7 | 20:56445111 | GCGAAGATCCATCTC[-/A]AAAAAAAAAAAGGTT | 57091 |
rs112135288 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CASS4 | GRCh38.p7 | 20:56433688 | CAGTCATTGTCCATC[A/G]GCTGTAGCTCAGCTC | 57091 |
rs112185885 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458886 | CCAAAGCTGGTAGTA[C/T]CAAGTGGCTAAGCAA | 57091 |
rs112215049 | snp | A/G | 3.30841e-05 | 0.00406706 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56445911 | CAAGGCCATCCTCAC[A/G]CTTCCCAGACCTGTC | 57091 |
rs112260070 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | CASS4 | GRCh38.p7 | 20:56447360 | GCTTGGGCCTGCCTG[A/C]TGGGCTGGGCTCCAG | 57091 |
rs112348553 | snp | C/G | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56448495 | TGACCCCAAGCTCAG[C/G]GGATACAACTCAAGT | 57091 |
rs112371637 | in-del | -/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56450032 | TCTTTTTTTTTTTTT[-/T]CTTTGAGATGGAGTT | 57091 |
rs112388864 | snp | G/T | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56450167 | CTCCCGAGTAGCTGG[G/T]ATTACAGTCATGCGC | 57091 |
rs112472677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56422955 | AAGGCTATTTGCATC[C/T]ATTTGGATGGGAGGG | 57091 |
rs112475294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442773 | TGGTGAAACTGCTTT[C/T]GGATCCACTAGTTCC | 57091 |
rs112583744 | snp | C/G/T | 0.000231959 | 0.0107672 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458672 | GTACCCCAGCCCTGC[C/G/T]GCGCTGGGGCACCTC | 57091 |
rs112634823 | snp | C/T | 0.00557542 | 0.0525036 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459609 | AGAGTCAAGCACACA[C/T]CACAATGGCAGAGAA | 57091 |
rs112722559 | in-del | -/A | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56451479 | GGGGGATGCATAGGG[-/A]GTTTGGTGGATGGAA | 57091 |
rs112730552 | snp | C/G | 0.00080036 | 0.0199885 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452408 | GAGCTAGCATCGTTT[C/G]CTCGTGCTCCACCAC | 57091 |
rs112798534 | snp | A/G | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56433328 | GCTGACTGCTTTGGG[A/G]TAGAGAGAACAGCAT | 57091 |
rs112875280 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447546 | AGTATGGCAAGCTGA[A/T]TCTTTCTCTTCTGGG | 57091 |
rs112895145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442383 | ACAGCTGATGAAGTA[C/T]GACTTCCATCACCCC | 57091 |
rs112956388 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56446404 | CCATTATTTATAATA[C/G]ATATTTAATATATGT | 57091 |
rs113033551 | snp | C/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56436280 | TCAGGCACCTGTACA[C/T]GACAGAGAGAGAGAT | 57091 |
rs113210891 | snp | A/G | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56426010 | ATTCTTGTAATGGCT[A/G]CATTGTACTCCATTA | 57091 |
rs113221226 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | CASS4 | GRCh38.p7 | 20:56449045 | CCATTGTGGAAGACA[A/G]TGTGGTGATTCCTCA | 57091 |
rs113302898 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | CASS4 | GRCh38.p7 | 20:56434745 | CACTGTGCCCGGTCC[C/G]ACAATTTATTTTTAA | 57091 |
rs113466561 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CASS4 | GRCh38.p7 | 20:56433687 | ACAGTCATTGTCCAT[C/T]GGCTGTAGCTCAGCT | 57091 |
rs113539482 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56451035 | TAAAATACAAAAATT[-/A]AAAAAAAAAAAAAAG | 57091 |
rs113541737 | in-del | -/G/GG | 0.338298 | 0.265141 | intron-variant | CASS4 | GRCh38.p7 | 20:56432896 | CCAAAAGTGTGGGCA[-/G/GG]GGGGCGTCACAGAAA | 57091 |
rs113548452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56436444 | ATATAGTGTGTGTGT[A/G]TATATATACATATAT | 57091 |
rs113602189 | snp | A/C | 0.00716266 | 0.059414 | utr-variant-5-prime, splice-acceptor-variant | CASS4 | GRCh38.p7 | 20:56412335 | TTCCCATGTGTTGTC[A/C]GATAGCTCCATAGAA | 57091 |
rs113632404 | snp | A/G | 0.0208155 | 0.0998723 | intron-variant | CASS4 | GRCh38.p7 | 20:56432896 | TCCAAAAGTGTGGGC[A/G]GGGGCGTCACAGAAA | 57091 |
rs113713882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443930 | CTTTGGAAAGCTGGG[A/C]TTCGAGAGCCTAGGA | 57091 |
rs113767090 | snp | C/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56430186 | TTTAGATGAGCACAT[C/T]GCACCTGCCAGCTGT | 57091 |
rs113902203 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | CASS4 | GRCh38.p7 | 20:56443413 | GGTGGAGGTTGCAGT[A/G]AGCCGAAATGGCACC | 57091 |
rs113933220 | in-del | -/A | 0.375 | 0.216506 | intron-variant | CASS4 | GRCh38.p7 | 20:56451476 | GTCAGGGGGATGCAT[-/A]GGGGTTTGGTGGATG | 57091 |
rs113988684 | snp | C/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56428382 | GCTTTGGGGTAAAGA[C/T]TGCCCATTCAGTGAG | 57091 |
rs114321469 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | CASS4 | GRCh38.p7 | 20:56447310 | GCAATAATCAAACTT[C/T]CTAGTTCATTTAAAG | 57091 |
rs114371038 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CASS4 | GRCh38.p7 | 20:56418646 | GAAGGAGAATCGTGT[A/G]CTCTGTCTTTAAAAA | 57091 |
rs114511457 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CASS4 | GRCh38.p7 | 20:56456896 | TTCGTATGTTGCCAA[A/G]GCTAGTCTCAAACTC | 57091 |
rs114783957 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CASS4 | GRCh38.p7 | 20:56424836 | AGAAGACAGGAATGA[G/T]CTGGCAAAAATGGAG | 57091 |
rs114789244 | snp | A/C | 0.133093 | 0.220981 | intron-variant | CASS4 | GRCh38.p7 | 20:56441306 | GCCTATTTACTTAAA[A/C]ATTGTTTTAATTTAT | 57091 |
rs114987291 | snp | A/G | 0.00434777 | 0.0464218 | intron-variant | CASS4 | GRCh38.p7 | 20:56451779 | TCGCGCCCTCTTTGG[A/G]AAGCTACTAACCCGG | 57091 |
rs114995219 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CASS4 | GRCh38.p7 | 20:56422797 | ATGTGCCATTCTCCA[C/T]GATTATTTTTAGAGG | 57091 |
rs115098039 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | CASS4 | GRCh38.p7 | 20:56443165 | GGTGTGGCGGGTGCA[C/T]AGCTTGTCAGACCGG | 57091 |
rs115147732 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56431203 | TGCCTCTGAGATTTC[A/G]TAGAAATAGGTAATA | 57091 |
rs115210125 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | CASS4 | GRCh38.p7 | 20:56418766 | AGCTTCTATTTATGT[C/G]TGTTACGTTTGATTC | 57091 |
rs115288617 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410102 | TGAGCTTAAGGGCAG[A/G]CTCTTCAGTATAGGG | 57091 |
rs115355790 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CASS4 | GRCh38.p7 | 20:56425537 | AGTTCAGGGAGGTAA[A/G]AAGTCTTCCTGCATG | 57091 |
rs115368655 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | CASS4 | GRCh38.p7 | 20:56433010 | TGGGGGCGTTATGTC[A/C]CGCCTCTCTTTCATT | 57091 |
rs115434949 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CASS4 | GRCh38.p7 | 20:56413166 | ACATAGCGAGACCCC[A/G]TCTTAAAAAAAAAAA | 57091 |
rs115590769 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | CASS4 | GRCh38.p7 | 20:56412836 | TCTGGACCCCAAAGA[C/G]ACTCAGTGCCACTCT | 57091 |
rs116044858 | snp | A/C | 0.105924 | 0.204309 | intron-variant | CASS4 | GRCh38.p7 | 20:56445769 | TGAAGAGCCTGCCAG[A/C]GGGGGTGCCGGGCGA | 57091 |
rs116102287 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56428933 | CCCGACCTGCCCCCC[A/C]GCCCTGACATTCTTG | 57091 |
rs116103961 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | CASS4 | GRCh38.p7 | 20:56451539 | AGAGAAACCAGTTTG[C/G]GTAAAATTAAATACA | 57091 |
rs116179410 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CASS4 | GRCh38.p7 | 20:56432718 | CTCTAAAACTCTAGT[C/T]CCTTAAATACTTCAT | 57091 |
rs116200782 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CASS4 | GRCh38.p7 | 20:56422872 | TTCTCTCATATCCCT[C/T]CTCATATCCAAGTTC | 57091 |
rs116295761 | snp | G/T | 0.0444908 | 0.142359 | intron-variant | CASS4 | GRCh38.p7 | 20:56433453 | CACACAGGGCCTTGA[G/T]GGTTTGGGCACAGTT | 57091 |
rs116297152 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CASS4 | GRCh38.p7 | 20:56426404 | ATTCCCGAGGCGTTG[A/G]CTAAACAGTGGACAA | 57091 |
rs116392899 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | CASS4 | GRCh38.p7 | 20:56431132 | TGACCTTGGACAAGT[C/T]ATTTGATCTCTCTGA | 57091 |
rs116425344 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CASS4 | GRCh38.p7 | 20:56425969 | TTTGGAGATTGTCCC[A/G]TTTCCATTGACATAA | 57091 |
rs116452604 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | CASS4 | GRCh38.p7 | 20:56448386 | CTTTGCTCTCCTCCC[C/G]CTGGTCCTGACCCTG | 57091 |
rs116543306 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56451441 | GGGAACATCTTACAA[C/G]AAGGCTGGCATTTCG | 57091 |
rs116727246 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CASS4 | GRCh38.p7 | 20:56416942 | AAATTCAGCCTCAAT[G/T]AAAGAGCAAATCTTT | 57091 |
rs116762689 | snp | C/G | 0.029116 | 0.117091 | intron-variant | CASS4 | GRCh38.p7 | 20:56445568 | GCAAGCTTGTTAACA[C/G]TGCAGGTTCCCGGCC | 57091 |
rs116883472 | snp | C/G/T | 6.61872e-05 | 0.00575238 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452211 | GGAACAGCAGAACAC[C/G/T]AAGCCCAATATTTAT | 57091 |
rs116981881 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CASS4 | GRCh38.p7 | 20:56430955 | GCCACACTAGGAAGG[C/T]GACCTTTTGTTCTGA | 57091 |
rs117122382 | snp | A/T | 0.0360663 | 0.129354 | intron-variant | CASS4 | GRCh38.p7 | 20:56413651 | GCATTCCGGCCTGGG[A/T]GACAGAGCAAGACTC | 57091 |
rs117258063 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | CASS4 | GRCh38.p7 | 20:56430843 | GGTCTGAGGTGGAAG[C/T]AACCTCAGGGCATTT | 57091 |
rs117271682 | snp | A/G | 0.00557542 | 0.0525036 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459810 | AACACTTATGTATTG[A/G]ATGCCTACTACATGC | 57091 |
rs117301565 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CASS4 | GRCh38.p7 | 20:56429897 | AACTTCCTGTATTTT[A/G]TTTCTCATAACTTCT | 57091 |
rs117311092 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | CASS4 | GRCh38.p7 | 20:56436174 | CACAGAACTGCCAAT[A/C]CAATTCAGAAGGAAA | 57091 |
rs117467809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56417608 | CTGCATCTCCGGTGC[C/T]TACAACAGTGCCTGC | 57091 |
rs117524862 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CASS4 | GRCh38.p7 | 20:56428801 | GTCAGATGGATGCGA[A/G]TTTGAATCCCTGCTC | 57091 |
rs117590692 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CASS4 | GRCh38.p7 | 20:56437686 | CTTCAGATCAAACAC[A/G]CAAAACGGGAGCCCA | 57091 |
rs117641527 | snp | A/T | 0.0792508 | 0.182605 | intron-variant | CASS4 | GRCh38.p7 | 20:56441610 | AACTCCGTCTCAAAA[A/T]AATAATAATAATTTT | 57091 |
rs117681842 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411273 | AGGCCGGGGCCAGGC[A/G]TTGTGGCTCACGCCT | 57091 |
rs117961040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56428681 | GTCTTTAAACCAGCT[C/T]TTTCTGGATTTGCAC | 57091 |
rs117972517 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | CASS4 | GRCh38.p7 | 20:56435344 | TAATGAGTTTAAAAG[G/T]TGTAATTAAATTTAT | 57091 |
rs118063704 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CASS4 | GRCh38.p7 | 20:56424430 | CCACTGCAATTCATG[A/G]GGGAAAAGAAAAGTT | 57091 |
rs137858744 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458924 | GCATTGACTTACCCC[A/G]CAGGGGGTCAGGAAA | 57091 |
rs137992530 | snp | A/G | 0.000510814 | 0.0159733 | missense | CASS4 | GRCh38.p7 | 20:56458410 | CCCGCTTATCTGAAC[A/G]CTGCCGGCTCTACTT | 57091 |
rs138064885 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CASS4 | GRCh38.p7 | 20:56455886 | CGGTGAGCTGAGATC[A/G]CACCACTGCACTCCA | 57091 |
rs138076361 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CASS4 | GRCh38.p7 | 20:56427698 | ACTTCAGGGATTCAC[A/G]TTTCCCATGTATCAA | 57091 |
rs138129057 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CASS4 | GRCh38.p7 | 20:56450205 | CCAGGCTAATTTTGT[A/G]TTTTTAATAGAGTTC | 57091 |
rs138151448 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56419330 | TTGTTCAGGGGAAGA[A/G]CAGCCTTGTACACAC | 57091 |
rs138177487 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56438989 | AGGAAGGGGAACTGG[G/T]TAAAGAGAAAGGGAG | 57091 |
rs138191448 | snp | A/G | 0.000399441 | 0.0141266 | missense | CASS4 | GRCh38.p7 | 20:56412474 | ATGAAGGGAACAGGC[A/G]TCATGGACTGTGCGC | 57091 |
rs138213952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56451268 | GTGTGAAATTATGTA[A/G]TGGCTTCTTCTTACG | 57091 |
rs138226603 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56415349 | CCCCCACCCACCCAC[A/G]CAGTACCAGGAAACA | 57091 |
rs138371775 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | CASS4 | GRCh38.p7 | 20:56422072 | TGTTACTTGCCTCCT[A/C]CTTCGGTGGGTTTTT | 57091 |
rs138464146 | snp | C/T | | | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452694 | TGGGACTGCCTGTAA[C/T]CTCACTGACAGTAAC | 57091 |
rs138503620 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56428317 | GGACAGAGTAGAGAC[A/T]GCCTCAAACTGTGGG | 57091 |
rs138506168 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CASS4 | GRCh38.p7 | 20:56435493 | AATGAACATGTATTG[A/C]TATAAAAAGATTGGG | 57091 |
rs138561366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56448324 | TAGTATTTACTATGA[C/T]GATTGAGTTTTTTGG | 57091 |
rs138573024 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56422396 | AGTCACCTGTTCCCC[A/C]GGTGTATATTGTCAG | 57091 |
rs138636863 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CASS4 | GRCh38.p7 | 20:56458166 | ATTATATATTACAGT[A/G]CTTTGAAAACATTAA | 57091 |
rs138711822 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56438685 | AACATAGTGAAACTC[C/T]GTCTCTATTAAAATA | 57091 |
rs138787078 | snp | A/C | 0.0558544 | 0.157504 | intron-variant | CASS4 | GRCh38.p7 | 20:56443434 | AAATGGCACCACTGC[A/C]CTCTAGCCTGGGTGA | 57091 |
rs138835221 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56446858 | TTGAGAACCACAGTT[A/C]CAGTCTAAATAAAAT | 57091 |
rs138854202 | snp | A/G | 4.97996e-05 | 0.00498972 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452247 | CCCTAAAGCAACGTC[A/G]AGTGTTTCTCAGGCT | 57091 |
rs138914750 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CASS4 | GRCh38.p7 | 20:56419992 | AGGTTGTGGTGAGCC[A/G]AAATCACGCCATTGC | 57091 |
rs138991387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420236 | CAGCTTTTGTTTGCT[C/T]TACATGTTCTGGACA | 57091 |
rs139063252 | snp | C/T | 8.25921e-05 | 0.00642567 | missense | CASS4 | GRCh38.p7 | 20:56445927 | CTTCCCAGACCTGTC[C/T]GGGCCTCACTGCCGA | 57091 |
rs139194067 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CASS4 | GRCh38.p7 | 20:56438812 | CAGTGAGCTGAGATC[A/G]CACCATTGCTCCCCA | 57091 |
rs139317043 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56433378 | TCAGAAAGGGTGACA[A/C]CCTGGAGGCCAGTGA | 57091 |
rs139334899 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CASS4 | GRCh38.p7 | 20:56436588 | AAAGGTACACAGGTA[C/T]GAATTTCTACCCCAC | 57091 |
rs139403781 | snp | A/C | 0.000153988 | 0.00877328 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452456 | CCAGCTCTTCCTCGG[A/C]GGAGTCAGCAAAGGA | 57091 |
rs139419603 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CASS4 | GRCh38.p7 | 20:56429068 | ACCCGGGCAGTGTGT[C/T]CACCCCGGCCTAGAG | 57091 |
rs139441315 | snp | C/T | 0.000245838 | 0.0110842 | intron-variant | CASS4 | GRCh38.p7 | 20:56451791 | TGGAAAGCTACTAAC[C/T]CGGCAACTATGTGTG | 57091 |
rs139441797 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56445186 | AAAATTCAAACTCCT[C/T]CACTGACCTGCTCCC | 57091 |
rs139479108 | snp | A/G | 0.117188 | 0.211804 | intron-variant | CASS4 | GRCh38.p7 | 20:56441530 | GAATCGCTTGAACCC[A/G]GGAAGTGGAAGTTGC | 57091 |
rs139483698 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448764 | ATGTTTTTTAATTAC[A/T]GTACACATTACATAT | 57091 |
rs139591745 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56412858 | TGCCACTCTAACTGT[C/G]CTATTTGGTTTCTGT | 57091 |
rs139616154 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56416181 | CAGCCTCCCAAGTAG[C/G]TGGGATTACAGGCAT | 57091 |
rs139658783 | snp | C/T | 0.046775 | 0.145601 | intron-variant | CASS4 | GRCh38.p7 | 20:56456648 | CCAAAGTGCTGGGAT[C/T]ACAGGTGTGAGTCAC | 57091 |
rs139719252 | snp | A/G | 0.0240643 | 0.107019 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459655 | TTGTATTTTTAGTAG[A/G]GTCGGGGTTTCACCA | 57091 |
rs139731473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420369 | AAGTGAAAAGTGCTT[C/T]GTGGAATGTTCACTT | 57091 |
rs139836473 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56424259 | TAAACTAATTCTCTC[A/C]CACATTAGGCATGAC | 57091 |
rs139872829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56423935 | ATCATTTTCTGCACA[C/T]TCTGGAGCTTTTCAT | 57091 |
rs140036604 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56432957 | TAGGAGCGCTCATCC[C/T]GGTGTTTGTGATTTC | 57091 |
rs140084676 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56439962 | GCTCCCTGAGGCATG[C/T]GCTGTGGGGGCCCCA | 57091 |
rs140104775 | snp | C/G | 1.64803e-05 | 0.00287052 | missense | CASS4 | GRCh38.p7 | 20:56458553 | GACACGCTGTGCATG[C/G]AGACCCAGGAGAGGG | 57091 |
rs140144032 | snp | C/T | 1.66704e-05 | 0.00288703 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452354 | CAACTTCCCCATCTC[C/T]TGAACCGGACAGATT | 57091 |
rs140151545 | snp | C/T | 0.000461893 | 0.0151899 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452622 | TGCAATCCACAGGTC[C/T]ACTGATCACATAGAA | 57091 |
rs140252002 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | CASS4 | GRCh38.p7 | 20:56434871 | CTATGCAAAAGAAAA[G/T]ATCTGGAAACACAAA | 57091 |
rs140254749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414032 | TAAACTTCATTATGT[A/G]TCTCCTAAGAACAAG | 57091 |
rs140289066 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CASS4 | GRCh38.p7 | 20:56426461 | AGTGCGACAGACACT[C/G]CTTTCAGGGCGAACA | 57091 |
rs140344582 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56416973 | TTTGTCTCTCTCCCA[C/T]CTCAACTCTGAGTGG | 57091 |
rs140416187 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437437 | CAGGTGCCCACTCTA[C/T]CCCGCCCTCCCACTC | 57091 |
rs140427912 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | CASS4 | GRCh38.p7 | 20:56437687 | TTCAGATCAAACACG[C/G]AAAACGGGAGCCCAG | 57091 |
rs140440915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421468 | TTGGGAGGCTGCAGT[A/G]GGAGGATCGCTTGAG | 57091 |
rs140450802 | snp | G/T | 3.30071e-05 | 0.00406232 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452152 | TTTCCTTTGGATGAA[G/T]ATGTCAGCTACAAGG | 57091 |
rs140548928 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56450068 | TGGAGTTTCGCTCCC[A/G]TTGCCCAGGCTGGAG | 57091 |
rs140568690 | snp | A/G/T | 5.00725e-05 | 0.00500341 | missense | CASS4 | GRCh38.p7 | 20:56445982 | TGCCTACCCAGCACC[A/G/T]GGGCCCCGTGGTCCT | 57091 |
rs140643810 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418182 | GAGGAGAAAACAGGG[A/G]GATCTGATGGAGGCG | 57091 |
rs140672660 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CASS4 | GRCh38.p7 | 20:56429989 | TTGATTAGAATTTGT[C/T]TCCTCCACTAACATG | 57091 |
rs140730428 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | CASS4 | GRCh38.p7 | 20:56454054 | GGCATGGTGGTGTGC[C/G]CCTGTAATTCCAGCT | 57091 |
rs140730707 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414941 | TGAGTGCTCTACTTG[A/C/G]ATTTTCTCACTATTA | 57091 |
rs140753551 | snp | C/T | 0.000168237 | 0.00917007 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458654 | TAAGAATGCCGTGCT[C/T]ACGTACCCCAGCCCT | 57091 |
rs140764617 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CASS4 | GRCh38.p7 | 20:56433238 | GTCAAGAGGGTGTCA[A/G]GGACCCTTTTTCTAA | 57091 |
rs140779644 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | CASS4 | GRCh38.p7 | 20:56435060 | CCTGGGATCTCAGCT[C/G]TATTAGATTTTGTGG | 57091 |
rs141059634 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414074 | ACAGAACGTAGAAGA[A/T]TATCTACATATCATC | 57091 |
rs141114997 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CASS4 | GRCh38.p7 | 20:56430790 | AGGAGGAGGATCTGG[C/T]GGAAGAGAGTTCTGG | 57091 |
rs141139244 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CASS4 | GRCh38.p7 | 20:56456125 | CACTTCTCAGTGGAG[A/G]CCCGGGGCACCGTTG | 57091 |
rs141253006 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | CASS4 | GRCh38.p7 | 20:56441861 | TTTCTAAATACTTTC[G/T]TCTTCCTCTACTCTG | 57091 |
rs141299799 | snp | A/C/T | 7.37631e-05 | 0.00607263 | missense | CASS4 | GRCh38.p7 | 20:56458692 | TGGGGCACCTCCAGG[A/C/T]GGAGGCTGAGAAGCT | 57091 |
rs141311296 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CASS4 | GRCh38.p7 | 20:56420164 | TCTCCACGAGTTTAT[A/G]TTAGTGAATGTATTG | 57091 |
rs141340009 | snp | C/T | 1.66638e-05 | 0.00288645 | missense | CASS4 | GRCh38.p7 | 20:56458352 | TAGAATCCTGGCCCT[C/T]TTATACCTCAGCCTT | 57091 |
rs141449328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56415915 | TTTTATAGAACAAGG[C/T]GAAATTTTTTTAAAA | 57091 |
rs141509053 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | CASS4 | GRCh38.p7 | 20:56428928 | TACCCCCCGACCTGC[C/G]CCCCAGCCCTGACAT | 57091 |
rs141525889 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CASS4 | GRCh38.p7 | 20:56432038 | TCAATTAATAGGGAA[C/T]CAATGAAATGTTAAA | 57091 |
rs141579948 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438906 | GGAATTCTGTATGTG[A/C]GTGTGTATGTGCATG | 57091 |
rs141611114 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56454877 | TGATTCTTTGTCCTT[C/T]ATTTTAGCAAGAGAG | 57091 |
rs141641872 | snp | G/T | 0.000153988 | 0.00877328 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452440 | TCCACCGACGACTCC[G/T]CCAGCTCTTCCTCGG | 57091 |
rs141645352 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56428687 | AAACCAGCTCTTTCT[A/G]GATTTGCACACATTT | 57091 |
rs141648315 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CASS4 | GRCh38.p7 | 20:56457259 | AGATAATAGGTAAAT[A/G]CGAGCGTGTGAAATT | 57091 |
rs141955948 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CASS4 | GRCh38.p7 | 20:56446980 | TGGGAGGCCAAGGCA[A/G]GAGGATCACTTGACA | 57091 |
rs142010631 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | CASS4 | GRCh38.p7 | 20:56439995 | AATGTGCTACTCACC[A/T]TTCAGGCCTTCTCCA | 57091 |
rs142051536 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CASS4 | GRCh38.p7 | 20:56443597 | AGTGTAAAGAGGGAG[A/G]TCACAGAGCAGAGGA | 57091 |
rs142088206 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411700 | AAGTACAACACACAC[A/G]ATAAGTTTATTTGAT | 57091 |
rs142089678 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | CASS4 | GRCh38.p7 | 20:56449146 | ATCATGCTGCTATAA[A/G]GATACATGCACACGT | 57091 |
rs142134714 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56414068 | TCATCTACAGAACGT[A/T]GAAGAATATCTACAT | 57091 |
rs142225914 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410441 | CCACTGAATTGTATA[C/G]TTCAAAAAGGTGCAT | 57091 |
rs142247733 | snp | A/G | 0.000581082 | 0.0170354 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56453072 | TTCCACTAAGCAAAG[A/G]GAAGATGAACACTCT | 57091 |
rs142262463 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CASS4 | GRCh38.p7 | 20:56433315 | TGGGTGGAAAGCTGC[C/T]GACTGCTTTGGGGTA | 57091 |
rs142279519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56457121 | ATGAAGGTGCTTCTT[C/T]GAAGTATGCCTTCCT | 57091 |
rs142337319 | in-del | -/C | 0.191775 | 0.243125 | intron-variant | CASS4 | GRCh38.p7 | 20:56422612 | GGAATTTTTTTCTGG[-/C]CACAACCTCCTCCTC | 57091 |
rs142429715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456307 | TTTTTCACCTCCCTA[C/T]GGTTAATATTTTCAC | 57091 |
rs142458274 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56425593 | AAGATGGACTCAAAG[A/T]CAAAATTCCTTTCTA | 57091 |
rs142469486 | snp | C/T | | | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459162 | TTGAAGCAATTCTCC[C/T]GCCTCAGCCTCCAGA | 57091 |
rs142548728 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CASS4 | GRCh38.p7 | 20:56417510 | TATTAAGATCTGAAA[C/T]TATCTCACTTTGTTT | 57091 |
rs142575228 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438724 | TAGCTGGGCATGGTG[A/G]CAGGCACCTGTAATT | 57091 |
rs142749187 | snp | C/T | 4.99979e-05 | 0.00499965 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452339 | GGTTCTCCAGACGGA[C/T]AACTTCCCCATCTCC | 57091 |
rs142769327 | snp | A/G | 5.0671e-05 | 0.00503318 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437441 | TGCCCACTCTACCCC[A/G]CCCTCCCACTCCAGG | 57091 |
rs142792670 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CASS4 | GRCh38.p7 | 20:56451166 | TAATTACGTGGTTGG[A/G]ATAAGTCGTTTAACT | 57091 |
rs142811598 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452838 | TGACAGTGTCCAGAA[C/T]AGCCCAGATGACCTT | 57091 |
rs142858434 | snp | C/G | 0.0013853 | 0.0262818 | intron-variant | CASS4 | GRCh38.p7 | 20:56412530 | TGAATGGGCTCTGGC[C/G]GGGAGCAAGCTGTGA | 57091 |
rs142890117 | snp | C/G | 0.00184945 | 0.030353 | intron-variant | CASS4 | GRCh38.p7 | 20:56437149 | CAAATTCTCTTCTCC[C/G]CTCTCCACCCACAGG | 57091 |
rs142933347 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CASS4 | GRCh38.p7 | 20:56448694 | GCAAAACCTATTTTG[G/T]TGCTCTCTTGCCTTG | 57091 |
rs142952498 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CASS4 | GRCh38.p7 | 20:56454228 | AAAGAAATACTTTTC[C/T]GGATGAGTTCAGACA | 57091 |
rs143052505 | snp | A/G | 4.94262e-05 | 0.00497098 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458486 | CAGCAGCCAGCCCGC[A/G]GAGATCATCACTCAG | 57091 |
rs143104441 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CASS4 | GRCh38.p7 | 20:56437928 | TCACCAGGACTGCCA[A/G]TGACAAATGGGAGGG | 57091 |
rs143180254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456075 | GCTTCTGGTCCAAGG[A/G]CCTCACTTGGAAAGC | 57091 |
rs143238032 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56423978 | ACCTTTTTCAAAAAC[A/G]GGGCTGAAGCAGAAA | 57091 |
rs143283513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56450465 | CCATTACAGCATCAT[A/G]ACCAAAAGCACCGAA | 57091 |
rs143303778 | snp | A/G/T | 0.00398691 | 0.0444912 | intron-variant | CASS4 | GRCh38.p7 | 20:56415532 | AGCAACTACCAATAC[A/G/T]TACTGGTGTTCAGTT | 57091 |
rs143418478 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412098 | TCGAAGTAGGAACTT[C/T]GCCCTATAAAGCAGA | 57091 |
rs143453295 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | CASS4 | GRCh38.p7 | 20:56434963 | TGTTTGCTTATTATT[A/T]TTTTTACTTTTTCTT | 57091 |
rs143531088 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CASS4 | GRCh38.p7 | 20:56434735 | AGACATGAGCCACTG[G/T]GCCCGGTCCCACAAT | 57091 |
rs143544086 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56430314 | AATGCATATTCATTT[C/T]CCTTTTCCCTCTCCC | 57091 |
rs143738001 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416407 | GGAGGATAAGTGGGC[A/T]TATTATACGTAAGTT | 57091 |
rs143746875 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56451992 | AAGGCCCCACGCTCT[C/T]CCCAGTTCCAGCTCC | 57091 |
rs143783871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56453301 | ATGAAATCTTATTAA[C/T]AAGTCAGATAAAGAT | 57091 |
rs143832676 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CASS4 | GRCh38.p7 | 20:56442313 | TTAGAACAACTCTTC[A/G]TTTTACAGATGAGGA | 57091 |
rs143861124 | snp | C/G | 0.000774 | 0.0196571 | missense | CASS4 | GRCh38.p7 | 20:56458449 | TCTTCAAAGCCATCA[C/G]CGCATTTCACGGCAG | 57091 |
rs143949951 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | CASS4 | GRCh38.p7 | 20:56449865 | TAAATATGAATGATA[A/C]AACAGGAAAATTTCT | 57091 |
rs143992087 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56435550 | AAACAAGTTGCCTTC[A/G]TGTAATTACAGTGGA | 57091 |
rs144060950 | snp | C/T | 0.0256215 | 0.110247 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410130 | GGGAAGAATCACTGC[C/T]GGGAGTCTGCCAAGT | 57091 |
rs144183325 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CASS4 | GRCh38.p7 | 20:56444249 | ATAGAGGGACCCTGA[C/T]CCAGTCCTCAGAAAC | 57091 |
rs144188603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56441636 | ATTTTTAATTTCTTG[A/C]CTTCTCTGTGCTTGG | 57091 |
rs144311461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446431 | ATGTATGTGTGTACA[C/T]ACACACACATTTTTT | 57091 |
rs144383380 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CASS4 | GRCh38.p7 | 20:56420485 | CCTCAAACTCCTGGG[C/T]TCAAGCAATCCTCCT | 57091 |
rs144420438 | snp | A/G | 1.69467e-05 | 0.00291085 | missense | CASS4 | GRCh38.p7 | 20:56446000 | GCCCCGTGGTCCTGA[A/G]GGTGAGCCTTGTTCA | 57091 |
rs144472163 | snp | C/T | 1.68422e-05 | 0.00290187 | missense | CASS4 | GRCh38.p7 | 20:56458656 | AGAATGCCGTGCTCA[C/T]GTACCCCAGCCCTGC | 57091 |
rs144489838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444459 | TTACCAGCCTGTGCC[C/T]AGCCTATATTCAGAC | 57091 |
rs144490566 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56428728 | GTTAGCAGATTAGAG[C/T]AGGAAACAGACTTGG | 57091 |
rs144494485 | snp | C/G | 0.000462657 | 0.0152024 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452194 | TTTCTGATTCCCCGA[C/G]TGGAACAGCAGAACA | 57091 |
rs144538897 | snp | A/C | 1.65274e-05 | 0.00287462 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452562 | CCTGATGCTCTTTGT[A/C]AGCAGGAAGTGGAGA | 57091 |
rs144553429 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56418389 | TCTGAGGTGTAAGCA[A/G]GATAACATAGGGCCT | 57091 |
rs144580872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56422511 | TATATTAAAGCATGT[C/T]GATCTGGGTAACACC | 57091 |
rs144600860 | in-del | -/A | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411547 | GAAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 57091 |
rs144615200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56428140 | TACTTGGATGGAAAC[A/G]GTCTCATGATCTCTA | 57091 |
rs144642600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56413066 | AAAGAAGCCAGGCAC[A/G]GTGGTACATACCTGT | 57091 |
rs144679127 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56436928 | AAGCATATTAGGACC[A/T]TCCGACCTCGTCTCA | 57091 |
rs144766268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56430068 | CAGAGCCCCTGGAAT[A/G]CACGTGATGCTCAAT | 57091 |
rs144798542 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432789 | AAACCCACTCCCAAC[A/G]CATTCAAGGGATAAT | 57091 |
rs144838825 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56431371 | TCTTTGCTACTGAAA[C/T]GCTGAGGCATAATTA | 57091 |
rs144842767 | snp | A/T | 1.65685e-05 | 0.00287819 | missense | CASS4 | GRCh38.p7 | 20:56445967 | CCCAGGTGTATGACG[A/T]GCCTACCCAGCACCG | 57091 |
rs144868085 | in-del | -/TA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436375 | GTATATATATATATG[-/TA]TATATATATATATAG | 57091 |
rs144872141 | in-del | -/TGCCTAT | 0.0134861 | 0.0810011 | intron-variant | CASS4 | GRCh38.p7 | 20:56445443 | TCTTAAAGTCCCCTC[-/TGCCTAT]TGCGTGCACTTCTCC | 57091 |
rs144898792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56437760 | GATGGAGAACTCAGC[A/G]GCCTCCACCCCCTTG | 57091 |
rs145004409 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CASS4 | GRCh38.p7 | 20:56434236 | AGAATTTATCCATGG[A/G]AATAAATAAGGGGAG | 57091 |
rs145010016 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | CASS4 | GRCh38.p7 | 20:56443399 | GCTTGAACCCGGGAG[A/G]TGGAGGTTGCAGTAA | 57091 |
rs145010731 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411214 | GGGATAGAACTTGAG[A/C]CTGGCTTGGAAGAAT | 57091 |
rs145141331 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CASS4 | GRCh38.p7 | 20:56446843 | ACTGAGCAGCCAGGA[C/T]TGAGAACCACAGTTC | 57091 |
rs145178900 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56445606 | ACACCCAGAGACTCC[A/G]TCCAACTCGCGTGGG | 57091 |
rs145191360 | snp | A/G | 5.0176e-05 | 0.00500854 | missense | CASS4 | GRCh38.p7 | 20:56458641 | TAGCGCTGGCCACTA[A/G]GAATGCCGTGCTCAC | 57091 |
rs145273287 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418783 | GTTACGTTTGATTCA[A/G]GAACACAATGTACCT | 57091 |
rs145280011 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56413840 | GAAAAATATGGGAAG[C/T]GTGGGGGTTATTCAG | 57091 |
rs145318031 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56446268 | ATTGTTTTTTCTTTT[C/T]CTTGTTGAGATGGGG | 57091 |
rs145340947 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56425488 | TTTGAGGGATGGCCA[G/T]TGAGAAGTAGTTGAC | 57091 |
rs145357449 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411779 | AGCCAGTACCCAGAA[A/G]ATGTTATTCATTAGG | 57091 |
rs145394252 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CASS4 | GRCh38.p7 | 20:56456938 | CGATCCTCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 57091 |
rs145531692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417076 | AGGTTGGTTTAAACA[A/C]GACAAAATGTGTTGG | 57091 |
rs145591378 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | CASS4 | GRCh38.p7 | 20:56417216 | TACCTTTAGCAGCTC[-/T]GAGGTGGTGAGCAAG | 57091 |
rs145633216 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CASS4 | GRCh38.p7 | 20:56429515 | CCTATAAACAGCATC[C/T]GCTATGGAAATTAGG | 57091 |
rs145646754 | snp | C/T | 7.60182e-05 | 0.00616468 | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412423 | AGCTGGAGATACTAG[C/T]TGCAGAGCTCAGGGG | 57091 |
rs145723326 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CASS4 | GRCh38.p7 | 20:56447168 | AGCTGAGATCACACC[A/G]CTGTACTCCAGCCTG | 57091 |
rs145761623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56430072 | GCCCCTGGAATACAC[A/G]TGATGCTCAATACAA | 57091 |
rs145762733 | snp | A/G | 1.64822e-05 | 0.00287068 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452651 | AAGAATCTGTAAGAG[A/G]ATTTCTGGATTTTGC | 57091 |
rs145821842 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411759 | CAGCATAGCCCTCAG[C/T]GCAGAGCCAGTACCC | 57091 |
rs145854634 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56415326 | GTCATCTCAGTTTAC[A/G]TAGGCCACCCCCACC | 57091 |
rs145864357 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56425305 | TTCTGTGACTCTTAA[C/T]GCACCTGCAGTTAGA | 57091 |
rs145924473 | snp | C/T | 1.65707e-05 | 0.00287838 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452229 | GCCCAATATTTATGA[C/T]ATCCCTAAAGCAACG | 57091 |
rs145967359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420357 | CTGGTTAACAGTAAG[C/T]GAAAAGTGCTTTGTG | 57091 |
rs145978651 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CASS4 | GRCh38.p7 | 20:56423706 | TGCACCACCATGCCC[A/G]GCTAATTTTTGTATT | 57091 |
rs145988272 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56422334 | TGAAGGCCTGAGAGA[C/T]CTTTATTGTTGCATC | 57091 |
rs146101941 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CASS4 | GRCh38.p7 | 20:56439851 | GCAGGCATTTCCTGC[C/T]ATCAGATGCTTTGCT | 57091 |
rs146122261 | snp | C/T | 0.000329669 | 0.0128345 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452603 | ATCTGGAGGCCAACA[C/T]TGATGCAATCCACAG | 57091 |
rs146123258 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CASS4 | GRCh38.p7 | 20:56424163 | ACTACTTAGCTATCA[C/G]CTCATTAAAAGAATT | 57091 |
rs146156375 | snp | C/T | 8.23811e-05 | 0.00641746 | missense | CASS4 | GRCh38.p7 | 20:56458542 | AGAAGCTGGTGGACA[C/T]GCTGTGCATGGAGAC | 57091 |
rs146244472 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56440241 | GGAACAACTGGCCCC[A/G]ATCTAGGCCTGGCAT | 57091 |
rs146257982 | snp | C/T | 1.66671e-05 | 0.00288674 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453082 | CAAAGGGAAGATGAA[C/T]ACTCTTCTGAACTAT | 57091 |
rs146467620 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56426211 | GCGTTGGCCCTTGAT[A/C]GCTGAACTACCTTAA | 57091 |
rs146595842 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56420691 | TGAGCCACCACACCC[A/G]GCCCAGGTTCAAAAG | 57091 |
rs146617358 | snp | A/G | 0.000198643 | 0.00996403 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451864 | ACCTTAAGAAGAGGC[A/G]GTTACAGCACATTAC | 57091 |
rs146635153 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56418477 | CTTAAAGCAGGAGAT[A/G]ACATGATCTAATTTA | 57091 |
rs146715351 | snp | A/G | 0.000310721 | 0.0124605 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437530 | GTCTATGAATTCCCC[A/G]ACCCTCCCACCAGTG | 57091 |
rs146799788 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CASS4 | GRCh38.p7 | 20:56438750 | TAATTCCAGCTACTC[A/G]GGAGACTGAGGCAGG | 57091 |
rs146837708 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CASS4 | GRCh38.p7 | 20:56453835 | GCTATGATGGTGCCA[C/T]TGCACTCCAGCCTTG | 57091 |
rs146849411 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CASS4 | GRCh38.p7 | 20:56417974 | CTTCATCTATTCCAC[A/G]AGGCAAAACAGCCCA | 57091 |
rs146872250 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CASS4 | GRCh38.p7 | 20:56450061 | TTTGAGATGGAGTTT[C/T]GCTCCCGTTGCCCAG | 57091 |
rs146946017 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CASS4 | GRCh38.p7 | 20:56442003 | CCTGAGGCTAAACCC[A/G]CCCAGAAAATACATT | 57091 |
rs146989197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56455267 | TAAGTAAAAACAATG[A/G]GTCCATTTAAAGGAA | 57091 |
rs147051631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56457421 | TAGGTACTGAAAATC[C/T]TTGAGAGTATGTAGG | 57091 |
rs147051647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56419009 | GCACACTTGGGGGGA[A/G]AAAAAGCTAAGGAGA | 57091 |
rs147074211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421535 | GACTATCTCTACAAA[A/C]AATTTTTAAAAGTAG | 57091 |
rs147216242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416480 | AAAATAGAGTCTGCA[A/G]TGTACTTTAGTGATT | 57091 |
rs147225996 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56419975 | TTGAACCCAGGAGGC[A/G]GAGGTTGTGGTGAGC | 57091 |
rs147324051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433218 | GTATGGGGAGAACTA[A/G]TTTGGTCAAGAGGGT | 57091 |
rs147345863 | snp | G/T | 6.85624e-05 | 0.00585461 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437464 | ACTCCAGGCCCCGTT[G/T]ATGAGCAGATGAGGA | 57091 |
rs147388572 | snp | A/G | 0.000649843 | 0.0180139 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452361 | CCCATCTCCTGAACC[A/G]GACAGATTATCAGGT | 57091 |
rs147429557 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56448697 | AAACCTATTTTGGTG[C/T]TCTCTTGCCTTGCTT | 57091 |
rs147439589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56451204 | TTTTATGGGCTGGGA[A/G]TATTAAGTGAGATAA | 57091 |
rs147563110 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CASS4 | GRCh38.p7 | 20:56413927 | GTGTGCATTTATTTG[C/T]GTATATTTAGACACT | 57091 |
rs147625590 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | CASS4 | GRCh38.p7 | 20:56457624 | TTCTGATATATCTCT[C/G]ATACTGAAATCAGAG | 57091 |
rs147658948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56425521 | TGTTTGGCATCCTGG[A/C]AGTTCAGGGAGGTAA | 57091 |
rs147668348 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CASS4 | GRCh38.p7 | 20:56429771 | ATGGAAGCTTCCATG[A/G]CTGCTTTCTCAGGTA | 57091 |
rs147762913 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | CASS4 | GRCh38.p7 | 20:56441758 | TGGGGACCTCCCAAC[A/T]CCCTTTGTGTTTCTC | 57091 |
rs147868938 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CASS4 | GRCh38.p7 | 20:56457160 | TCTAACTTCCCCTCC[A/G]ACCCTACTAGGAGAC | 57091 |
rs147898883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56454764 | CACTCACTCTCTAAA[A/G]CTTCTGATTCATACG | 57091 |
rs147940511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442129 | TTGTGAGGCACTTCA[C/T]GGACTCCTTTCTATA | 57091 |
rs147992661 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CASS4 | GRCh38.p7 | 20:56422750 | TCAATGTTATCATGG[A/G]GAACCAGTTAAAGTT | 57091 |
rs148023315 | snp | C/T | 9.97473e-05 | 0.00706142 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56437271 | ACACGTGCCAGAAAG[C/T]GAGGGTTGGTGGAAG | 57091 |
rs148110031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447250 | TAAAAAAAAAAGAAG[C/T]CACTTTAGCCTTGCT | 57091 |
rs148206287 | snp | A/G | 0.000790501 | 0.0198652 | missense | CASS4 | GRCh38.p7 | 20:56458451 | TTCAAAGCCATCAGC[A/G]CATTTCACGGCAGCC | 57091 |
rs148219392 | snp | A/G/T | 1.66158e-05 | 0.0028823 | synonymous-codon, missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452259 | GTCGAGTGTTTCTCA[A/G/T]GCTGGGAAGGAGCTG | 57091 |
rs148258264 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56450762 | CTTGGGGCCAGGCAC[A/G]GTGGCTGAAGCCTGT | 57091 |
rs148320388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56415552 | GGTGTTCAGTTCATA[C/T]TAGTGCAGTTGATCC | 57091 |
rs148445122 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56440427 | AAGGAAAACAGATGC[G/T]CTGTCCTCTGTTGGT | 57091 |
rs148497019 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56437022 | CAAATCAAAGAGCAG[A/G]GACAAGAGCCTCTGG | 57091 |
rs148515143 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | CASS4 | GRCh38.p7 | 20:56425332 | TAGATCCCATTTAAC[A/G]GTCATTCGTTGCCCT | 57091 |
rs148546989 | in-del | -/A | 0.117886 | 0.21224 | intron-variant | CASS4 | GRCh38.p7 | 20:56421830 | CTCACTTTTTTCCTT[-/A]AAAAAAGAAAAAAGG | 57091 |
rs148553170 | snp | C/T | 1.66596e-05 | 0.00288609 | missense | CASS4 | GRCh38.p7 | 20:56445981 | GTGCCTACCCAGCAC[C/T]GGGGCCCCGTGGTCC | 57091 |
rs148695172 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56444342 | CCAACTTGGAAAGCC[C/G]CCTACTGAGCAACAG | 57091 |
rs148725876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456999 | CCTGCTTCATTCTTA[C/T]ACTCCCTGCTTCCAA | 57091 |
rs148782954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56428818 | TTGAATCCCTGCTCT[C/G]CTACCTGCTGCTGCA | 57091 |
rs148884596 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CASS4 | GRCh38.p7 | 20:56430173 | TTGGCTGCTCGGGTT[C/T]AGATGAGCACATTGC | 57091 |
rs148885958 | in-del | -/GT | 0.0588605 | 0.161139 | intron-variant | CASS4 | GRCh38.p7 | 20:56432135 | TGAGGGGCTAGGTAG[-/GT]ATAGGCAATTTAATT | 57091 |
rs148921681 | snp | A/G/T | 0.00342143 | 0.041223 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452759 | TCTCCAACTCCTACC[A/G/T]CATCCTGCTTGAAAC | 57091 |
rs148955140 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CASS4 | GRCh38.p7 | 20:56419004 | ATAGAGCACACTTGG[A/G]GGGAAAAAAAGCTAA | 57091 |
rs148979504 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CASS4 | GRCh38.p7 | 20:56442150 | CCTTTCTATATCTGT[A/G]TTGACAGTCTGCAGA | 57091 |
rs149030803 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CASS4 | GRCh38.p7 | 20:56437768 | ACTCAGCGGCCTCCA[C/T]CCCCTTGTCGTTGAC | 57091 |
rs149219133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446529 | ATTATCTCTGGGGGA[A/G]GAAATTTTAGTTGTT | 57091 |
rs149223558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420722 | TGAGAGTCTCCCCAC[A/G]GTTGAAAGGGGAATA | 57091 |
rs149291458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413054 | TTTAGAAAGGTGAAA[A/G]AAGCCAGGCACGGTG | 57091 |
rs149315196 | snp | A/C | 0.0164242 | 0.0891197 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458758 | GATGAGGACTGTCTA[A/C]CTCCCTTCCTCCTCT | 57091 |
rs149504647 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | CASS4 | GRCh38.p7 | 20:56444218 | CCAGTGCTGCATCCC[A/G]GGGACACCATGATGA | 57091 |
rs149538981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456037 | TAATGTGCATTTCTA[C/G]CAAGTTTGCAGGTGA | 57091 |
rs149556703 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56438990 | GGAAGGGGAACTGGT[G/T]AAAGAGAAAGGGAGC | 57091 |
rs149703805 | snp | A/G | 0.00113968 | 0.0238441 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452192 | GCTTTCTGATTCCCC[A/G]AGTGGAACAGCAGAA | 57091 |
rs149841530 | snp | A/C/G/T | 0.00288712 | 0.0378906 | missense | CASS4 | GRCh38.p7 | 20:56445928 | TTCCCAGACCTGTCC[A/C/G/T]GGCCTCACTGCCGAC | 57091 |
rs149862612 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | CASS4 | GRCh38.p7 | 20:56424696 | CAGTGAGCAGAGATC[A/G]CACCACTGCATTCCA | 57091 |
rs149907943 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56420345 | GGTGTTTGCCATCTG[G/T]TTAACAGTAAGTGAA | 57091 |
rs150016338 | snp | C/T | 0.00208751 | 0.0322397 | missense | CASS4 | GRCh38.p7 | 20:56458604 | CGTGGCAGCAGTCAC[C/T]TCTGCAGCCTGCTCA | 57091 |
rs150073164 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CASS4 | GRCh38.p7 | 20:56456924 | CTCCTAGGGTTAAGC[A/G]ATCCTCCTGCCTCGG | 57091 |
rs150103772 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CASS4 | GRCh38.p7 | 20:56435232 | TTCCATTTTTGTAAC[A/G]GAATAGAGATATTAG | 57091 |
rs150196620 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56418686 | TTTGATGTTTGAGAC[C/T]GCTGGTCGCCGTGTC | 57091 |
rs150225841 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56454642 | AATTTGGTAAGTTGA[A/C]GGGATTTTATTTTTC | 57091 |
rs150241415 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CASS4 | GRCh38.p7 | 20:56414672 | ATTATACAGATAGGC[C/T]GGGAGCGGTGGCTCA | 57091 |
rs150330943 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432194 | CTAAGTATGAAACTG[A/G]TTAAAGTCCTACAAG | 57091 |
rs150389155 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | CASS4 | GRCh38.p7 | 20:56426834 | TCTGCTCACCTCAGC[C/T]TCCCAAAGTGCTGGG | 57091 |
rs150407383 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CASS4 | GRCh38.p7 | 20:56450109 | CGATCTTGGCTTACC[A/G]CAACCTCCACCTCCC | 57091 |
rs150459970 | snp | A/C/G | 0.000107382 | 0.00732678 | intron-variant | CASS4 | GRCh38.p7 | 20:56446030 | AGGGGCCCCTCATCA[A/C/G]CCAGACCTCTGCGCC | 57091 |
rs150631072 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56412760 | CGTCCATCATTTTGC[A/G]TCCAGCAAACTCCTG | 57091 |
rs150776710 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CASS4 | GRCh38.p7 | 20:56416088 | GGAGTTTCACTCTGT[C/T]GTCCAGGCTGGAGTG | 57091 |
rs150842021 | snp | C/T | 0.000396131 | 0.014068 | missense | CASS4 | GRCh38.p7 | 20:56458589 | CGCAACGAGATCCTC[C/T]GTGGCAGCAGTCACC | 57091 |
rs150901483 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438955 | CTGAGAAGAACATGC[C/T]CCAGGCATAGTTACC | 57091 |
rs150913821 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CASS4 | GRCh38.p7 | 20:56428950 | CCCTGACATTCTTGA[A/G]TTTCTGCAGCTTTGC | 57091 |
rs150951279 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56445713 | CGAGGAAGGCTGCCT[C/G]CACCGGGGAGCCTCC | 57091 |
rs150975958 | snp | A/G/T | 0.00478372 | 0.0487162 | intron-variant | CASS4 | GRCh38.p7 | 20:56430640 | GAACATGGGTGCAGG[A/G/T]TGAGTGCTGGCTGCT | 57091 |
rs151039647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56454229 | AAGAAATACTTTTCT[A/G]GATGAGTTCAGACAT | 57091 |
rs151045039 | snp | A/G | 0.00057644 | 0.0169673 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452914 | AGGTTTGCCTCCATT[A/G]TCATTGCCAATGGAA | 57091 |
rs151168171 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56414069 | CATCTACAGAACGTA[A/G]AAGAATATCTACATA | 57091 |
rs151198793 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | CASS4 | GRCh38.p7 | 20:56426364 | CAGTGCCTGACACAG[A/T]GTTGAGAACCCGCGA | 57091 |
rs151220889 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410809 | AATATTAATATATTA[C/T]TATTAATATAATTTA | 57091 |
rs151250486 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56421155 | AATCAAATGGAAGTG[C/T]CCTGACTGCAGGCAT | 57091 |
rs180686538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56424504 | CTAGCACTTTGGGAG[A/G]TCAAGGCGGGTGGAT | 57091 |
rs180751997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446757 | TGCCTGTGCCCCAAC[C/T]CCAGAGACTGTTGAA | 57091 |
rs180767301 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56436422 | CATATATATATCAAC[A/C]CGTCATATATAGTGT | 57091 |
rs180782932 | snp | C/T | 0.00852514 | 0.0647294 | intron-variant | CASS4 | GRCh38.p7 | 20:56458303 | CCACAGCCCATTGAT[C/T]GAATCTCCTATCTAT | 57091 |
rs181178988 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447593 | CCCCCACCTCCTACC[C/T]CTCACCTCCTTGCTG | 57091 |
rs181213213 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425120 | CTCTGGCCTGGGTCT[C/T]TGTACACAGTACTCA | 57091 |
rs181234075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56434901 | AAACCGAAGGATTAA[C/T]AGCAGTTACCTGTGG | 57091 |
rs181366801 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CASS4 | GRCh38.p7 | 20:56419869 | CCAACATGGAGAAAC[C/T]CCATCTCTACTAAAA | 57091 |
rs181376322 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56440275 | CAGCTGCTGTCTGAG[A/C]AGCTGACTCGGAGCA | 57091 |
rs181392797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56429610 | ATGCGCCCCCAACAC[A/T]TACATACACACTCAC | 57091 |
rs181413708 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56421165 | AAGTGCCCTGACTGC[A/C]GGCATGCCAGAGGAT | 57091 |
rs181441565 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CASS4 | GRCh38.p7 | 20:56441629 | AATAATAATTTTTAA[C/T]TTCTTGCCTTCTCTG | 57091 |
rs181533365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56431228 | GTAATATTATGACTT[A/C]AGTGCATCCAACACA | 57091 |
rs181617792 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412069 | GAATGCTGTGTGTTC[A/G]TACACTGAGCTCTTC | 57091 |
rs181699365 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56453479 | CTCCTTGCATTTTTG[A/T]AAGTTATAAATTTAG | 57091 |
rs181795951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416735 | AGAATTTCTGATATT[C/T]GATTCTATTTTAAAC | 57091 |
rs182003769 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | CASS4 | GRCh38.p7 | 20:56417041 | AATGTAGAATTTTTT[A/T]AAAAATCTTCCACAT | 57091 |
rs182008718 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56435202 | AGATGGTATTTTTCA[G/T]CATTGGTCTTCCAAT | 57091 |
rs182023799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56457997 | TCCAGCCTGGAAGAT[A/G]AAGGAAAACTCTGTC | 57091 |
rs182031709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420245 | TTTGCTCTACATGTT[C/T]TGGACAGCCCAGGCA | 57091 |
rs182089980 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56426590 | CGCCTCCCCCTCCCC[C/G]GCCAAGACAAGGTCT | 57091 |
rs182097839 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56448422 | AGGCCATCCACAGCA[C/G/T]GGCTGCCACCCTCTC | 57091 |
rs182327972 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56441190 | GTAGTGACAGGGTTT[C/T]GCCATGTTGGCCAGG | 57091 |
rs182340862 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446403 | GCCATTATTTATAAT[A/T]GATATTTAATATATG | 57091 |
rs182522388 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CASS4 | GRCh38.p7 | 20:56450464 | ACCATTACAGCATCA[C/T]GACCAAAAGCACCGA | 57091 |
rs182570277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56455192 | TTGGTTTCCTTCTAT[C/T]TGTGGTCAATGACAG | 57091 |
rs182594082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56424478 | AGGCATGGTGGCTCA[C/T]GCCTGTAATCCTAGC | 57091 |
rs182698534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417677 | TGAACGAATGGGAGC[C/T]TACAGGGAGTGCAGG | 57091 |
rs182899720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56418047 | TCAGCCATTCACCCA[A/G]TGCATAGTTATTGGG | 57091 |
rs182941031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421394 | TGCTAGACACAAAAC[C/T]CTTTAGAAACACAGG | 57091 |
rs182966397 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459619 | ACACACCACAATGGC[A/C]GAGAAAGGAAGAGCT | 57091 |
rs182984186 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56427252 | CCACCAGAAATCCCT[C/T]CCAGAAGAAGTGTCT | 57091 |
rs183034076 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CASS4 | GRCh38.p7 | 20:56413588 | TGAGGCACAAGAATC[A/G]CTTGAGCCTGGGAGG | 57091 |
rs183155890 | snp | A/G | 0.000982838 | 0.0221462 | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412450 | GGGGAGCTGCTCCAC[A/G]TCACCGACATGAAGG | 57091 |
rs183162861 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56431470 | ATATTGAGGGGAATC[C/G]TGTTATGGCAACATA | 57091 |
rs183167752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56454575 | ATATGAGAAAGAATG[A/C]TCAAGTCTAAAGTGA | 57091 |
rs183192139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56437073 | AGGGCATGATGAATT[C/T]GTATGAAGCTTTCTA | 57091 |
rs183305574 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432525 | GGCGTGCACCACCAC[A/G]CTGGACAATTTTTGT | 57091 |
rs183372958 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CASS4 | GRCh38.p7 | 20:56437710 | GAGCCCAGATTGCTG[G/T]CAATCACGCTCGGGG | 57091 |
rs183536927 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56414840 | TATTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 57091 |
rs183795045 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CASS4 | GRCh38.p7 | 20:56455899 | TCGCACCACTGCACT[C/T]CAGCCTGGGCAACAA | 57091 |
rs183843093 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56421995 | GCTGGATGGGAACTT[C/T]GGCGATTGCCCTGGG | 57091 |
rs183890056 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56451732 | AGCCACTGAAGGAGC[A/G]GCGGAGTGACGATGA | 57091 |
rs183922694 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56447842 | CAGGCGCTTGCCTTG[A/G]GTGTAAAAGTTATCA | 57091 |
rs183923723 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410203 | TAAGAGACTTGAATT[C/T]AGTTTCTGGGTCTGT | 57091 |
rs183928458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56429239 | GAAAGTGTGCGGGCC[A/C]GTTCCCTCTCTTCTT | 57091 |
rs183942743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56419730 | GCCACCGTGCCCGGC[A/T]AGGCTCTGCACTCTT | 57091 |
rs183953323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56439722 | TGAAAACTTTTTTTA[A/G]TAAGGAAAAGAATTA | 57091 |
rs183989594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56422641 | TCAAAGCCCCGTTAG[C/T]AGGCAGTGCCTCCTA | 57091 |
rs183996075 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56444839 | ATCGGGGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 57091 |
rs184032739 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56443542 | TTGTCCACCTAGACC[A/G]ATCAGCCTGAGACCA | 57091 |
rs184074365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56425822 | CAAACCTCTAACTCC[C/T]CAGACCCCTGTTTCC | 57091 |
rs184323585 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418693 | TTTGAGACCGCTGGT[C/T]GCCGTGTCGGGTGGG | 57091 |
rs184458275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56423632 | TCACTGCAACCTCCA[C/T]CTCCCAAGTTCAAGC | 57091 |
rs184483113 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56439276 | TGGCCTCCAGCAATC[A/C/G]TCCTGCTTCAGCCTC | 57091 |
rs184774950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56419916 | GGCTTGGTGGTGCAC[A/G]CCTGTAATCCCAAAT | 57091 |
rs184780857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56440390 | AAACAAAAAATCAAT[A/T]GCAATTCCTTCCTCT | 57091 |
rs184789605 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56416280 | GTCTCGAACTCCTGA[A/C]CTCAAGTTATCTGCC | 57091 |
rs184864612 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56456729 | TGTTGCTGAGGCTAG[A/C]GTGCAGTGGTGAGAT | 57091 |
rs184873002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456196 | CAGCATCCCAGAACC[C/G]CTGCCCGCTCACTGC | 57091 |
rs184907688 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56415729 | AGATAGCCTTTCAGA[C/T]CCTGAAGTTCGCCTT | 57091 |
rs184913136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433252 | AGGGACCCTTTTTCT[A/G]AGGAAGTGACATTTA | 57091 |
rs184961908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56434744 | CCACTGTGCCCGGTC[C/G]CACAATTTATTTTTA | 57091 |
rs185244339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413389 | ATAAAAGTGACTAGT[A/G]TGGCTGTCTGCGGTG | 57091 |
rs185254952 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56431551 | CTGTCCTGAAGACAG[C/G]AGGTCAAAATTACAA | 57091 |
rs185264137 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56454733 | ACAAAGACTTAGGAA[A/C]CATGGTAAGCTATAG | 57091 |
rs185417721 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | CASS4 | GRCh38.p7 | 20:56457928 | GCTGAGGCAAGAGAA[A/T]TGCTTGAACCCAGAA | 57091 |
rs185507183 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442244 | TAAGAGAGGCGTCTA[A/T]GTGTCAGAATCAGAC | 57091 |
rs185520173 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424479 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCTAGCA | 57091 |
rs185547445 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421312 | ACAGTTGTTTTTTAA[G/T]TGACTCAATTTGTTA | 57091 |
rs185629257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450908 | GTGTGGTAGTGGGCG[C/T]CTGTAATCCCAGCAC | 57091 |
rs185702263 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56428589 | ACCCAAATGTCTTAC[A/G]CCTGGCCTGTCTCAC | 57091 |
rs185754600 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56446769 | AACCCCAGAGACTGT[C/T]GAATCAGGTCTAGAT | 57091 |
rs185795940 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56424821 | GCACAAGGGACAAAG[A/C]GAAGACAGGAATGAG | 57091 |
rs185965438 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56416742 | CTGATATTTGATTCT[A/C]TTTTAAACCTACTTT | 57091 |
rs186063139 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56458056 | TAAATATAGTCATTG[C/T]CAATGTGTTTCTTAA | 57091 |
rs186073690 | snp | A/G | 0.116838 | 0.211584 | intron-variant | CASS4 | GRCh38.p7 | 20:56441380 | GAGGCCAAGGCGGGT[A/G]GATCACCTGAGGTCA | 57091 |
rs186089155 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56417344 | CTCCTGCCTCAGTTC[C/T]TTCCCCTTCTCCCCT | 57091 |
rs186097408 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435265 | AAGAAGCACAATAAT[G/T]TTCAACAAACATAAT | 57091 |
rs186179221 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56430365 | CATTTGGGGGAAATG[A/T]CCTTTTTGGAAATCG | 57091 |
rs186199949 | snp | A/G | 0.029116 | 0.117091 | intron-variant | CASS4 | GRCh38.p7 | 20:56420438 | TTGTCACCCAGACTG[A/G]AGTGCAGTGGCGTTA | 57091 |
rs186272732 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56447645 | CCTCCAGGTGGACAA[A/C]TGCATCTCCTCTGGC | 57091 |
rs186338077 | snp | C/T | 0.000115315 | 0.00759236 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452794 | GAAAGCTTGGATAAT[C/T]GCAATTGGCCTCTGG | 57091 |
rs186368328 | snp | C/T | 0.0103295 | 0.0711199 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412130 | GAGTGGTGTTTTTTT[C/T]TTCTTCTTCTTCTTT | 57091 |
rs186405167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417914 | TTGAAATCAAGGTCA[C/T]AAAGACCTGTAGCCT | 57091 |
rs186498175 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411299 | CGCCTGTAATCCCAG[C/G]ATTTTGAGAGGCTGA | 57091 |
rs186603772 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56426837 | GCTCACCTCAGCCTC[C/T]CAAAGTGCTGGGATT | 57091 |
rs186611109 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56448791 | ATATATAATATGTTA[A/T]GTCATATATATATCT | 57091 |
rs186625188 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56436571 | GGGTAGCTAATTTGC[C/T]TAAAGGTACACAGGT | 57091 |
rs186880027 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56435125 | TCTGATTCTTCTTAC[A/C/G]CTTTTTAGATAGACT | 57091 |
rs186898369 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56422952 | ACAAAGGCTATTTGC[A/C]TCCATTTGGATGGGA | 57091 |
rs186903662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445058 | GAGTTTGCAGTGAGC[C/T]GAGATCGCGCCATTG | 57091 |
rs186986396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56426171 | AGCACACTCCAGACC[C/T]AAAACTGCCTGCATT | 57091 |
rs187096832 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56425503 | GTGAGAAGTAGTTGA[C/T]GATGTTTGGCATCCT | 57091 |
rs187202229 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CASS4 | GRCh38.p7 | 20:56448055 | GCTGAGGCAGGAGAG[C/T]GGCGTGAACCCGGGA | 57091 |
rs187271820 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56453855 | CTCCAGCCTTGGTGA[A/C]AGAGCAAGAGCTAAT | 57091 |
rs187459507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442745 | TATTTCAAGAGAAAA[G/T]GGTCAGATTTCCTGG | 57091 |
rs187460707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56431329 | CACATGCATTTCATT[C/T]GTCTTTTGTAACATT | 57091 |
rs187468744 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414976 | CTCACAACATCCTCA[A/T]GAAGCAGAGGTATTA | 57091 |
rs187474653 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | CASS4 | GRCh38.p7 | 20:56432663 | ATGCACCATCACACC[C/G]AGCCTAAGTCTTGAC | 57091 |
rs187555509 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56418714 | GTCGGGTGGGGAGTG[A/G]TTGTGAGCAGAAAAA | 57091 |
rs187673129 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56418061 | AATGCATAGTTATTG[A/G]GCTCCGGGGGTTCAG | 57091 |
rs187682754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56437083 | GAATTTGTATGAAGC[A/T]TTCTAAGAGAGTGGG | 57091 |
rs187709212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56418444 | GCCATTCTAATTGCA[A/G]AGGAAACCACCAGCC | 57091 |
rs187738357 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444067 | TCCTGTTCGCATTGC[A/G]GCTGCTTTGTCTGCA | 57091 |
rs187774816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56438305 | AAAAAAAAAAAAAGT[A/G]TATCCCCTTCAATGC | 57091 |
rs187777625 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56439341 | GCCTGGCCTAAAGTA[C/T]CAATTTTTAAAAACA | 57091 |
rs187801198 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56432410 | TCTCACTTCCTCACC[C/G]AGGCTGTAGTGCAGT | 57091 |
rs188016041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56422083 | TCCTCCTTCGGTGGG[C/T]TTTTCATGAGCAAGG | 57091 |
rs188072193 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413724 | GGAATTTGTGACTGA[A/G]TAACCCATGACAGTC | 57091 |
rs188139907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56455232 | ATTTACCATTTTTCA[C/T]AGTTTCCTTTAAATT | 57091 |
rs188209752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56429372 | CAGCTCCTCCCCAAA[A/G]CTAACAAAATCCAGC | 57091 |
rs188270733 | snp | A/G | 0.000362665 | 0.0134611 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451889 | CATTACCAAATCCTC[A/G]GAAATCGGAATGGAT | 57091 |
rs188283545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56456053 | CAAGTTTGCAGGTGA[C/T]GTTGATGCTTCTGGT | 57091 |
rs188310735 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56434180 | GGCAACGTGACAGCA[A/T]CCGGAGCCCTGATGG | 57091 |
rs188319174 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CASS4 | GRCh38.p7 | 20:56456309 | TTTCACCTCCCTACG[G/T]TTAATATTTTCACTT | 57091 |
rs188447223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56415740 | CAGACCCTGAAGTTC[A/G]CCTTTGTACATCGTA | 57091 |
rs188548419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56450534 | ACTGGAATAGGGAGT[A/G]TTCGTGATGTGTAGC | 57091 |
rs188803892 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447260 | AGAAGTCACTTTAGC[C/T]TTGCTAGGCTCAGTT | 57091 |
rs188821081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56427287 | ATACTTTGATTTTTC[C/T]TCAGGTTGTCCTTCC | 57091 |
rs188894913 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56457950 | AACCCAGAAGGTGGA[C/G]GTTGCAGTAAGCTGA | 57091 |
rs188915180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417028 | GGATCAAGGTAAAAA[C/T]GTAGAATTTTTTAAA | 57091 |
rs188922422 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435172 | CTAATCCACACAGAC[C/T]TGCTTGTCTGGTTAA | 57091 |
rs188968766 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CASS4 | GRCh38.p7 | 20:56419771 | TAGGAGGCCAGGCAC[A/G]GTGGCTCATGCCTGT | 57091 |
rs188976519 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440104 | CCCTGGGCTACAAGA[C/T]ATAGAACCAGACAGT | 57091 |
rs189173495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446733 | ATCTGAGAGCTTTAG[C/T]CATCCTGGTGCCTGT | 57091 |
rs189197922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56440875 | CCACAGTAAAACCCC[C/G]CAGGGGAATTTCCTG | 57091 |
rs189349362 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409770 | GATATTATGCAAGCA[C/T]CCAGTTTCCTAGACT | 57091 |
rs189426370 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56434846 | TGACTCTAGGTGTGT[A/G]TGTGAACAACTATGC | 57091 |
rs189499511 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56424501 | ATCCTAGCACTTTGG[G/T]AGGTCAAGGCGGGTG | 57091 |
rs189670762 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56413498 | ATCAACATGAAAAAA[A/C]CCCATATCTACCAAA | 57091 |
rs189680368 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56432162 | TAATTAAGGCATATT[A/G]GAGTGTGATTGCAAG | 57091 |
rs189688880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56454900 | CAAGAGAGTCCTGGA[G/T]ATCACTGAGTCTAAT | 57091 |
rs189710925 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CASS4 | GRCh38.p7 | 20:56456781 | CCACCCAGGTTCAAT[C/T]GATTCTCCCACCTCA | 57091 |
rs189728984 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436189 | CCAATTCAGAAGGAA[A/T]ATAGCAAAAACCAGA | 57091 |
rs189737755 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56458236 | AAACCATGCTTTTTT[A/T]AAAAAAATAAAAAGT | 57091 |
rs189746680 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56416567 | TGTGTGTATGCACAC[A/T]TGCCATTACAGGTAA | 57091 |
rs189790252 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CASS4 | GRCh38.p7 | 20:56426519 | ATCTAAAAGATTAAA[A/G]AGGATTTTTCCCTCT | 57091 |
rs189899388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56424371 | TGACAATTCCTCATA[A/G]CTTAAGGAATTTTAC | 57091 |
rs189999295 | snp | A/T | 1.64738e-05 | 0.00286995 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452908 | ATCAAGAGGTTTGCC[A/T]CCATTGTCATTGCCA | 57091 |
rs190036262 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411735 | GAGAGAGAATACAGG[A/T]GCGGGGCTCAGCATA | 57091 |
rs190116164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424988 | GAAAGTAGGGACATG[A/G]TTATTCTGAATGTTT | 57091 |
rs190161896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446100 | TCAGCATTACCATGG[C/T]GGCCAGGGGCTCAGC | 57091 |
rs190245032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56431091 | AAGGTGAAAGAATGG[A/G]TGTGAGGAACCAATT | 57091 |
rs190281887 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CASS4 | GRCh38.p7 | 20:56428796 | CTTCAGTCAGATGGA[C/T]GCGAGTTTGAATCCC | 57091 |
rs190488754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56451428 | CCCAAGGTCATTAGG[A/G]AACATCTTACAAGAA | 57091 |
rs190493245 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56420068 | ACAAACAAAAGAAAG[C/G]TCCTCTAGGAGATGA | 57091 |
rs190604615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56418071 | TATTGGGCTCCGGGG[A/G]TTCAGGGTGATCAAG | 57091 |
rs190658288 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421381 | GGAAGCAGGCAGTTG[C/G]TAGACACAAAACCCT | 57091 |
rs190712824 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442371 | TCGTGCAGCCACACA[C/G]CTGATGAAGTACGAC | 57091 |
rs190767176 | snp | A/G | 0.000246635 | 0.0111021 | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412429 | AGATACTAGCTGCAG[A/G]GCTCAGGGGAGCTGC | 57091 |
rs190770327 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56421066 | TGGAAAAGTTTGGTG[A/C]ACAAGCCTGAACCTT | 57091 |
rs190790663 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56417603 | CAGTGCTGCATCTCC[A/G]GTGCCTACAACAGTG | 57091 |
rs190868742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56448348 | TTTTTGGTGCCCTCT[C/T]AATGTTGTGCCCAAG | 57091 |
rs191018185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56431388 | CTGAGGCATAATTAA[C/T]TGATTGCATGAGCTG | 57091 |
rs191027043 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CASS4 | GRCh38.p7 | 20:56441519 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAA | 57091 |
rs191229625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56434182 | CAACGTGACAGCATC[C/T]GGAGCCCTGATGGTT | 57091 |
rs191240147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456466 | GCAATCTCCGCCTCA[C/G]AGGTTCGGGCGATTC | 57091 |
rs191329938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56436845 | TGAGCCAAGATTTCA[C/T]CGCTGCACTCCAGCC | 57091 |
rs191485193 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409779 | CAAGCACCCAGTTTC[C/G]TAGACTAATAGTTCT | 57091 |
rs191495791 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56428959 | TCTTGAGTTTCTGCA[C/G]CTTTGCTCTTTTGAG | 57091 |
rs191531292 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56425815 | CTAATCCCAAACCTC[C/T]AACTCCCCAGACCCC | 57091 |
rs191556769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417946 | CCTCCAGCATTTCCC[A/C]GCAACTTCCTCCCTT | 57091 |
rs191568729 | snp | C/T | 0 | 0 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458923 | GGCATTGACTTACCC[C/T]GCAGGGGGTCAGGAA | 57091 |
rs191797879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56426880 | CACCGCACCCAGCCA[A/G]CTTCTCCCCCTTATT | 57091 |
rs191798340 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56447782 | GCCATGCCTGGTCCA[C/T]GACAAACACACAAGC | 57091 |
rs191807985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56450315 | AGGCGTGAGCCACCA[C/T]GCCCGGCTGAGAAGT | 57091 |
rs192048887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56443327 | ACAAAAAAGTAGCGG[A/G]GTGTGGTGGCGGGCA | 57091 |
rs192164707 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CASS4 | GRCh38.p7 | 20:56422095 | GGGTTTTTCATGAGC[A/G]AGGGTGAAATTGTCA | 57091 |
rs192165208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445357 | CCCTGCCTCAGCCCA[G/T]GTGACAAGTCCTTAG | 57091 |
rs192411797 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56418527 | GCTGCTGTGCAACAG[A/C]TGGGCTGTAAGTAGG | 57091 |
rs192446475 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56454465 | CATGTGGGTCATTAT[A/G]TCAGGCCATGTTGAT | 57091 |
rs192453896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421615 | GTGGGAGGATCGTTC[A/G]AGCCCAGGAGTTCGA | 57091 |
rs192465591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56451445 | ACATCTTACAAGAAG[A/G]CTGGCATTTCGCCGT | 57091 |
rs192557655 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | CASS4 | GRCh38.p7 | 20:56444446 | GGCCCTGTCTTGCTT[A/T]CCAGCCTGTGCCCAG | 57091 |
rs192569376 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CASS4 | GRCh38.p7 | 20:56415891 | ATTTATTCTATTTTT[A/T]AAAAATTGTTTTATA | 57091 |
rs192606149 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56415594 | CTTAATGCCTACATT[A/G]TTGCTCAATTGCTTT | 57091 |
rs192612816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433162 | TGGATGAGTTGAACC[C/T]TAATGTGACACGTAC | 57091 |
rs192680589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456074 | TGCTTCTGGTCCAAG[A/G]ACCTCACTTGGAAAG | 57091 |
rs192743632 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CASS4 | GRCh38.p7 | 20:56438307 | AAAAAAAAAAAGTAT[A/G]TCCCCTTCAATGCAG | 57091 |
rs192797251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56439635 | GAGCTATTATTACTA[C/T]GGCGCCCCTGCACTC | 57091 |
rs192825049 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56428588 | CACCCAAATGTCTTA[C/G]GCCTGGCCTGTCTCA | 57091 |
rs192928791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56455338 | GTATAACTTGTAAAG[A/G]TTGTAAAGGTTGTCT | 57091 |
rs192943271 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CASS4 | GRCh38.p7 | 20:56414673 | TTATACAGATAGGCC[A/G]GGAGCGGTGGCTCAT | 57091 |
rs193000626 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56419570 | TAGCTGGGGCTTCAG[A/G]CATGCACCACTGTGC | 57091 |
rs193035877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450537 | GGAATAGGGAGTGTT[C/T]GTGATGTGTAGCCAT | 57091 |
rs193177403 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56432460 | GCAACCTCCACCTCC[C/T]GGGCTCAAGCCATCC | 57091 |
rs199513148 | snp | C/T | 3.29533e-05 | 0.00405901 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452944 | AGGCTCCTTTTTAAG[C/T]GGAACTGTGAAAAGG | 57091 |
rs199573867 | snp | C/T | 0.000320873 | 0.0126623 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437440 | GTGCCCACTCTACCC[C/T]GCCCTCCCACTCCAG | 57091 |
rs199621598 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455133 | ATGTTCTTCCTTTTT[A/T]AAAAAAAAAAAAGTC | 57091 |
rs199624123 | in-del | -/CAG | | | upstream-variant-2KB, cds-indel | CASS4 | GRCh38.p7 | 20:56411997 | CTAGTGGCCTCTCAT[-/CAG]GGAAATGAGCTTGGT | 57091 |
rs199670261 | snp | A/C | 0.000329468 | 0.0128306 | missense | CASS4 | GRCh38.p7 | 20:56458431 | GGCTCTACTTTGGGG[A/C]GCTCTTCAAAGCCAT | 57091 |
rs199737719 | in-del | -/T | 0.0197687 | 0.0974348 | intron-variant | CASS4 | GRCh38.p7 | 20:56417474 | CCACCGCCAACACTC[-/T]TCATCTATCTTACCT | 57091 |
rs199741474 | snp | A/G | 0.000151587 | 0.00870462 | missense | CASS4 | GRCh38.p7 | 20:56458704 | AGGCGGAGGCTGAGA[A/G]GCTGGAGCAACACAC | 57091 |
rs199775680 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456537 | TGCCACCACACCCGG[C/G]TAATTTTTTGTATTT | 57091 |
rs199808780 | snp | C/G/T | 0.000757657 | 0.019449 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452021 | CCACTTTCTACAATC[C/G/T]TCCAAGTGGCAGATC | 57091 |
rs199963878 | in-del | -/G/GG/GGGGCA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432900 | AAGTGTGGGCAGGGG[-/G/GG/GGGGCA]NCGTCACAGAAATCT | 57091 |
rs200024288 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56451022 | AAAATACAAAAATTA[A/T]AAAAAAAAAAAAAGA | 57091 |
rs200048841 | snp | A/G | 0.0016465 | 0.028645 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451910 | CGGAATGGATTTATG[A/G]CACTCCAGTGTCTCC | 57091 |
rs200155192 | snp | A/G | 9.46226e-05 | 0.00687767 | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412456 | CTGCTCCACATCACC[A/G]ACATGAAGGGAACAG | 57091 |
rs200170755 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457772 | TAATCCCAGCACTTT[A/T]AGGAGGCTGAGGTGG | 57091 |
rs200192753 | snp | C/T | 4.94214e-05 | 0.00497074 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452807 | ATCGCAATTGGCCTC[C/T]GGAAGTTCTTGTGAC | 57091 |
rs200228453 | snp | A/G | 0.000166423 | 0.0091205 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452530 | CTGCAGCACAAGGTG[A/G]TCAGCTCTGTCGCTG | 57091 |
rs200292143 | snp | G/T | 3.35621e-05 | 0.00409633 | intron-variant, synonymous-codon | CASS4 | GRCh38.p7 | 20:56437427 | GGAGACCTATCAGGT[G/T]CCCACTCTACCCCGC | 57091 |
rs200320164 | snp | A/G | 0.00018459 | 0.00960526 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452454 | CTCCAGCTCTTCCTC[A/G]GAGGAGTCAGCAAAG | 57091 |
rs200326642 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56451509 | AAAGAAAGGGTTGCC[-/A]AGGGCATTTAGAGCA | 57091 |
rs200560887 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456088 | GGACCTCACTTGGAA[A/G]GCCCCCGCTTTAGAC | 57091 |
rs200561357 | in-del | -/TA | 0.0260105 | 0.111035 | intron-variant | CASS4 | GRCh38.p7 | 20:56414865 | GCAGGAGAATTGCTT[-/TA]TATATATATATATAA | 57091 |
rs200563468 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447223 | AAAAAAAAAAAAATC[A/G]AAATCAAAAATTAAA | 57091 |
rs200660833 | snp | C/T | 4.96356e-05 | 0.0049815 | missense | CASS4 | GRCh38.p7 | 20:56445910 | CCAAGGCCATCCTCA[C/T]GCTTCCCAGACCTGT | 57091 |
rs200781135 | in-del | -/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413185 | TAAAAAAAAAAAAAA[-/G]AAAAGAAAAGTTAAA | 57091 |
rs200829230 | snp | C/T | 0.000337815 | 0.0129921 | intron-variant | CASS4 | GRCh38.p7 | 20:56458337 | CTTCCTTCCCTTCTT[C/T]AGAATCCTGGCCCTC | 57091 |
rs200859679 | snp | A/T | 0.000410137 | 0.0143143 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453105 | TGAACTATTAAAGAA[A/T]AATAGGGCAAATATC | 57091 |
rs200864987 | in-del | -/AA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56451021 | TAAAATACAAAAATT[-/AA]AAAAAAAAAAAAAGA | 57091 |
rs200892131 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438288 | GTGAGAACCTGTTTT[C/T]AAAAAAAAAAAAAAG | 57091 |
rs200928361 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440978 | CCTATTTATTTACTT[-/A]AAAAAAAAAATTTTT | 57091 |
rs200949271 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452095 | AAAAAACTCAGCCTT[C/T]CAGAAATTCCTTCTT | 57091 |
rs200954227 | in-del | -/ATTT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434454 | TTTATTTATTTATTT[-/ATTT]GAGATGGAGTCTCAC | 57091 |
rs201029608 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448908 | TCAAAACCACCATGA[G/T]CTACCATCTCACACC | 57091 |
rs201033878 | snp | C/G | 3.34952e-05 | 0.00409225 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56437418 | CAGCTCAGAGGAGAC[C/G]TATCAGGTGCCCACT | 57091 |
rs201078486 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454343 | TGCTACTTTCAGCCC[A/C]GACCTTTGTGTTCTG | 57091 |
rs201106876 | snp | C/G | 5.27691e-05 | 0.00513632 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458663 | CGTGCTCACGTACCC[C/G]AGCCCTGCCGCGCTG | 57091 |
rs201199213 | in-del | -/ACC | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435902 | CTACAGGCATGCGCT[-/ACC]ACTCTGCCCAGCTAA | 57091 |
rs201200517 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441003 | ATTTTTTTTTTTTTT[C/T]TTGGAGGCAGAATCT | 57091 |
rs201314210 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432700 | TCAATACTCTTTATA[-/A]GACTCTAAAACTCTA | 57091 |
rs201359000 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453010 | AAGTGTGAAAAATAC[A/G]TCCAGCCTCCCCAAA | 57091 |
rs201366703 | snp | C/T | 0.000280008 | 0.011829 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452864 | ACCTTGAGAGGTTTG[C/T]CATGGTGGCACGGAT | 57091 |
rs201383535 | snp | A/G/T | 0.000441314 | 0.0148482 | intron-variant | CASS4 | GRCh38.p7 | 20:56451777 | ACTCGCGCCCTCTTT[A/G/T]GAAAGCTACTAACCC | 57091 |
rs201454304 | snp | G/T | 1.64825e-05 | 0.00287071 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452659 | GTAAGAGAATTTCTG[G/T]ATTTTGCCCGAGGAG | 57091 |
rs201482500 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435512 | AAAAAGATTGGGAAA[G/T]GTGATTACTTTAAAA | 57091 |
rs201499624 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56451938 | TCCAGGAAAGGCCAG[C/T]GTCAGAAACACGCCT | 57091 |
rs201501428 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432897 | CAAAAGTGTGGGCAG[-/C]GGGCGTCACAGAAAT | 57091 |
rs201516954 | snp | C/T | 5.4804e-05 | 0.00523441 | intron-variant, synonymous-codon | CASS4 | GRCh38.p7 | 20:56437529 | AGTCTATGAATTCCC[C/T]GACCCTCCCACCAGT | 57091 |
rs201532998 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438289 | TGAGAACCTGTTTTC[A/C]AAAAAAAAAAAAAGT | 57091 |
rs201594401 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436338 | GATTGCTATATATAT[A/G]TGTGTGTGTGTGTGT | 57091 |
rs201645295 | snp | A/T | 0.00199806 | 0.0315443 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453007 | TTTAAGTGTGAAAAA[A/T]ACATCCAGCCTCCCC | 57091 |
rs201650745 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455127 | ACTTGATGTTCTTCC[-/T]TTTTTTAAAAAAAAA | 57091 |
rs201656713 | in-del | -/TTG | 0.00676609 | 0.0577691 | intron-variant | CASS4 | GRCh38.p7 | 20:56413962 | CACACTTCATTTTTA[-/TTG]TTGTTGTTAAACTCT | 57091 |
rs201734849 | snp | C/T | 1.72668e-05 | 0.00293822 | intron-variant | CASS4 | GRCh38.p7 | 20:56450579 | CATTCAAGTTGTCTG[C/T]CTTTGTGGTCTTTCC | 57091 |
rs201738538 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457017 | TCCCTGCTTCCAAGA[A/G]TCCATGTGAACTGAC | 57091 |
rs201757934 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417458 | TTCCCCCCTACACAG[C/G]CCCACCGCCAACACT | 57091 |
rs201823830 | snp | A/G | 1.64743e-05 | 0.00287 | missense | CASS4 | GRCh38.p7 | 20:56458448 | CTCTTCAAAGCCATC[A/G]GCGCATTTCACGGCA | 57091 |
rs201858337 | in-del | -/AAAC | 0.0134861 | 0.0810011 | intron-variant | CASS4 | GRCh38.p7 | 20:56455935 | GACTCTGTCTCAAGA[-/AAAC]AAACAAACAAACAAA | 57091 |
rs201872765 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458749 | GGACACTGGGATGAG[A/G]ACTGTCTACCTCCCT | 57091 |
rs201927658 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434618 | TTTTTTTTTTTTTTT[-/T]GTATTTTTAGTAGAG | 57091 |
rs201945789 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | CASS4 | GRCh38.p7 | 20:56442045 | CGGCTGTTGGTAGAC[-/G]GGGCAACTCTGAGCC | 57091 |
rs202007264 | snp | C/T | 0.000189624 | 0.00973529 | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412432 | TACTAGCTGCAGAGC[C/T]CAGGGGAGCTGCTCC | 57091 |
rs202050647 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435311 | TTTGCTTTATTTATG[-/A]AAAGTATGAACAAAG | 57091 |
rs202058938 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458462 | CAGCGCATTTCACGG[C/T]AGCCTCAGCAGCAGC | 57091 |
rs202098954 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436372 | TGTGTATATATATAT[A/G]TGTATATATATATAT | 57091 |
rs202122566 | snp | C/T | 5.02651e-05 | 0.00501299 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452479 | GCAAAGGAGCTCTCC[C/T]TGGACCTGGATGTGG | 57091 |
rs202139822 | in-del | -/T | 0.133093 | 0.220981 | intron-variant | CASS4 | GRCh38.p7 | 20:56441168 | TAAATTTTTTTTGTA[-/T]TTTTTAGTAGTGACA | 57091 |
rs202201331 | snp | A/C | 1.66421e-05 | 0.00288458 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56437328 | GGCCCCTGCCAACCG[A/C]CTCCAAATCCTCACG | 57091 |
rs207477658 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419816 | GGGAGGCCAAGGCAG[G/T]TGGATCATCTGAGGT | 57091 |
rs267606009 | snp | A/G | | | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452337 | ATGGTTCTCCAGACG[A/G]ACAACTTCCCCATCT | 57091 |
rs367556996 | snp | C/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410227 | GGTCTGTTACTTTAC[C/T]CTGTGACCTTGGGCA | 57091 |
rs367557991 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425098 | TCCCATCATGGGAGG[C/T]CCTCCTCTCTGGCCT | 57091 |
rs367569172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447869 | ATCAATGGGCCGGGC[A/G]CGGTGGCTCACGCCT | 57091 |
rs367581178 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56437076 | GCATGATGAATTTGT[A/G]TGAAGCTTTCTAAGA | 57091 |
rs367625281 | snp | C/T | 4.94238e-05 | 0.00497086 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451967 | CTCTCACCAGCTTTG[C/T]GGAAGAATCAAGGCC | 57091 |
rs367669347 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436013 | CTCCTCGGCCCCCCA[A/G]AGTGCTGGGATTACA | 57091 |
rs367757855 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419306 | CCAAACATAACGCCT[A/G]TGAAGTGTTTGTTCA | 57091 |
rs367783265 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442063 | GCAACTCTGAGCCAC[A/G]GGTTTTGAACTGTTT | 57091 |
rs367891442 | snp | C/T | 1.76761e-05 | 0.00297283 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458666 | GCTCACGTACCCCAG[C/T]CCTGCCGCGCTGGGG | 57091 |
rs367927326 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CASS4 | GRCh38.p7 | 20:56425963 | CTACATTTTGGAGAT[G/T]GTCCCGTTTCCATTG | 57091 |
rs367988042 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448411 | ACCCTGAGAACAGGC[A/C]ATCCACAGCACGGCT | 57091 |
rs368021333 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410324 | CAGTGGTTTCCAGGG[A/G]CTGGGGGAAGAACAA | 57091 |
rs368082221 | snp | C/G | 4.98451e-05 | 0.004992 | missense | CASS4 | GRCh38.p7 | 20:56437275 | GTGCCAGAAAGCGAG[C/G]GTTGGTGGAAGTGTT | 57091 |
rs368083547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56418178 | GAAAGAGGAGAAAAC[A/G]GGGGGATCTGATGGA | 57091 |
rs368141375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442820 | TCTGTCTCCCTAAAC[C/G]TTTCGAAACTGTGTT | 57091 |
rs368180345 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420354 | CATCTGGTTAACAGT[A/G]AGTGAAAAGTGCTTT | 57091 |
rs368214217 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413453 | CAAGGCAGGTGGATC[A/G]CTTGAGGCCAGGAGT | 57091 |
rs368270565 | snp | A/G | 0.000100073 | 0.00707295 | missense | CASS4 | GRCh38.p7 | 20:56437350 | ATCCTCACGGAGGTC[A/G]CTGCAGACAGGCCGT | 57091 |
rs368398046 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427596 | CTCGATGTTGAGTCT[A/G]GGCACAGCTACCTCA | 57091 |
rs368404273 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436767 | CGGCACGCATGTGTA[G/T]TCCCAGCTACTTGGG | 57091 |
rs368500669 | snp | A/T | 0.000153988 | 0.00877328 | missense | CASS4 | GRCh38.p7 | 20:56458377 | AGCCTTCGAGTCAAC[A/T]GACTCCTGAGAGGAA | 57091 |
rs368527507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56418772 | TATTTATGTGTGTTA[C/T]GTTTGATTCAGGAAC | 57091 |
rs368582691 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413886 | CCTTCACCTAGATCA[C/T]TGGTTTCTGGTACTT | 57091 |
rs368784416 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448879 | ATCATCACTGGCCGT[A/C]AGAGAAATGCAAATC | 57091 |
rs368803428 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409675 | GATAGCACATTTGCC[A/G]AGAGCATTAAGATTA | 57091 |
rs368949451 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427009 | ATCTTTGCTGTAACT[C/T]CCTAAGCTAGGCATG | 57091 |
rs369121137 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456499 | CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGACTAC | 57091 |
rs369135463 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411418 | CAGGCGTGGTGGCGG[A/G]TGCCTGTAATCCCAG | 57091 |
rs369138889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56455161 | GTCAAAGATGTTATC[A/G]TTGTGCTTATTTTTA | 57091 |
rs369235380 | snp | C/G | 1.89896e-05 | 0.0030813 | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412422 | AAGCTGGAGATACTA[C/G]CTGCAGAGCTCAGGG | 57091 |
rs369237200 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417176 | GCTTCGTTTGTGAGT[A/G]GAGAGCAGTTTTAGG | 57091 |
rs369296515 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421292 | ATGGGTAACATCGCT[A/G]AGGGACAGTTGTTTT | 57091 |
rs369392986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56434739 | ATGAGCCACTGTGCC[C/T]GGTCCCACAATTTAT | 57091 |
rs369451188 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444994 | ATGTGCCTGTAGTCC[-/C]AGCTACTCAGGAGGC | 57091 |
rs369498099 | in-del | -/AC | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415932 | AAATTTTTTTAAAAC[-/AC]GTGATATTAGTGATA | 57091 |
rs369501809 | snp | C/T | 2.02723e-05 | 0.00318366 | missense | CASS4 | GRCh38.p7 | 20:56458719 | AGCTGGAGCAACACA[C/T]GCGGCAGTTCAGAGG | 57091 |
rs369536191 | snp | C/G | 2.63967e-05 | 0.00363286 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458751 | ACACTGGGATGAGGA[C/G]TGTCTACCTCCCTTC | 57091 |
rs369540243 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450046 | CTTTTTTTTTTTTTC[C/T]TTGAGATGGAGTTTC | 57091 |
rs369554766 | snp | G/T | | | missense | CASS4 | GRCh38.p7 | 20:56458590 | GCAACGAGATCCTCC[G/T]TGGCAGCAGTCACCT | 57091 |
rs369609263 | snp | C/T | | | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452121 | TTCTTATGGCTTTCT[C/T]GTACCCAGAGGCACA | 57091 |
rs369732251 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447734 | CATTCCCTGAGCCAT[C/T]CCTCCCTGGCTCTTG | 57091 |
rs369739655 | snp | A/G | 0.000115427 | 0.00759606 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452081 | ATGTGCCCATGCAGA[A/G]AAAACTCAGCCTTCC | 57091 |
rs369776461 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413310 | TAGAACAGGAAAAAA[-/A]GAAATGAAACAAGCA | 57091 |
rs369794050 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56456534 | GCCTGCCACCACACC[C/T]GGCTAATTTTTTGTA | 57091 |
rs369852052 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415189 | TTATGCTTTGCAGGC[C/T]AAATACAATCTCTGT | 57091 |
rs369856027 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417633 | GCCTGCACAAAGTAG[G/T]TGCTCAATACATGCT | 57091 |
rs369890182 | snp | A/G | 0.000115315 | 0.00759236 | missense | CASS4 | GRCh38.p7 | 20:56458500 | CGGAGATCATCACTC[A/G]GAGCAAGCTGGTCAT | 57091 |
rs369911648 | in-del | -/CTT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426547 | CTTCTTCTTCTTCTT[-/CTT]TTTTTTCCCCCTTCT | 57091 |
rs369923817 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456521 | TGGGACTACAGGCGC[C/G]TGCCACCACACCCGG | 57091 |
rs369975585 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417713 | CCCTGGCTGCAGCCC[C/T]GCTGTGAGGATAGGA | 57091 |
rs369979619 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438871 | TCAAAAATAAACAAA[C/T]AAACAAAAAACTCTA | 57091 |
rs369992632 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459614 | CAAGCACACACCACA[A/G]TGGCAGAGAAAGGAA | 57091 |
rs370063702 | in-del | -/CAAA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455950 | AAACAAACAAACAAA[-/CAAA]AACAAACAAACTTGC | 57091 |
rs370093431 | in-del | -/GGT | | | cds-indel, intron-variant | CASS4 | GRCh38.p7 | 20:56451865 | CTTAAGAAGAGGCGG[-/GGT]TTACAGCACATTACC | 57091 |
rs370159907 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442675 | TAATTTAAAAAAAAA[-/A]CCCACCACATCAAGA | 57091 |
rs370172922 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416014 | GTGGAACTCTAGCCA[A/G]CTAGTCAACTCCATT | 57091 |
rs370178675 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447925 | AGGCAGGTAGATCAC[A/G]AGGTCAGGAGGTGGA | 57091 |
rs370180884 | snp | A/C | 1.71138e-05 | 0.00292516 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56437238 | CAGCAGAGGGGACAT[A/C]CTGACCATTCTGGAG | 57091 |
rs370232426 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456535 | CCTGCCACCACACCC[G/T]GCTAATTTTTTGTAT | 57091 |
rs370240600 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410228 | GTCTGTTACTTTACT[A/C/G]TGTGACCTTGGGCAA | 57091 |
rs370335675 | snp | A/G | 1.66239e-05 | 0.00288299 | missense | CASS4 | GRCh38.p7 | 20:56437303 | GTTTGCTCCATGGGA[A/G]GCAAGGCCTGGCCCC | 57091 |
rs370350171 | snp | C/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411294 | GCTCACGCCTGTAAT[C/G]CCAGCATTTTGAGAG | 57091 |
rs370351778 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413442 | CTTTGGGAGGCCAAG[A/G]CAGGTGGATCACTTG | 57091 |
rs370383528 | snp | C/T | 1.88596e-05 | 0.00307074 | intron-variant | CASS4 | GRCh38.p7 | 20:56446046 | CCAGACCTCTGCGCC[C/T]AGAGTCTGGGGTTCT | 57091 |
rs370400376 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418415 | GGCCTGGTCGGCCGT[A/G]TAAGAGCTTTGAAGC | 57091 |
rs370437353 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56419082 | AGGCATTGGCCGACA[C/T]GATAATGGAATGGGG | 57091 |
rs370506918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56457110 | CAATTCTAATAATGA[A/G]GGTGCTTCTTCGAAG | 57091 |
rs370524415 | snp | C/T | 0.000307953 | 0.0124049 | intron-variant | CASS4 | GRCh38.p7 | 20:56437120 | GTAGCAGTCACTGGC[C/T]ACGGTGCTAACTGCA | 57091 |
rs370729166 | snp | A/G | 0.000122552 | 0.00782695 | intron-variant | CASS4 | GRCh38.p7 | 20:56451793 | GAAAGCTACTAACCC[A/G]GCAACTATGTGTGGT | 57091 |
rs370799989 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409753 | CAGCCTTCAGACAAC[C/T]GGATATTATGCAAGC | 57091 |
rs370809310 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56422932 | TTTCTCTGGATAAAC[C/T]GGCCACAAAGGCTAT | 57091 |
rs370837602 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440282 | TGTCTGAGCAGCTGA[C/T]TCGGAGCAGAGCTTT | 57091 |
rs370854328 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416471 | TTAGTTACGAAAATA[C/G]AGTCTGCAATGTACT | 57091 |
rs370923868 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445778 | TGCCAGCGGGGGTGC[C/T]GGGCGACCCCTTCAG | 57091 |
rs370929246 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56445579 | AACACTGCAGGTTCC[C/T]GGCCCCCCTCGACAC | 57091 |
rs370988993 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411692 | GGGGTTTCAAGTACA[A/G]CACACACGATAAGTT | 57091 |
rs370989161 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56430161 | ACCACTGTATCCTTG[A/G]CTGCTCGGGTTTAGA | 57091 |