SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs371141970 | snp | A/T | 1.64738e-05 | 0.00286995 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452825 | AAGTTCTTGTGACTG[A/T]CAGTGTCCAGAACAG | 57091 |
rs371150425 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452728 | CAGAACAGAATTCGG[A/G]ACCAGATGCAGACCA | 57091 |
rs371161350 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56434585 | GGGTCTACAGGTGCA[C/T]GCCACCACTCCCAGC | 57091 |
rs371163356 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424576 | GGAAACCCCGTCTCT[A/G]CTAAAAATACAAAAA | 57091 |
rs371164856 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447340 | GCTAAAGCTCCTGCT[A/G]CCCAGCTTGGGCCTG | 57091 |
rs371173627 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56430992 | TTCTAAGCAATTAGA[A/G]GTTTTTAAAATAAGA | 57091 |
rs371177644 | snp | A/C/G | 0.000116162 | 0.00762021 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452244 | CATCCCTAAAGCAAC[A/C/G]TCGAGTGTTTCTCAG | 57091 |
rs371368402 | in-del | -/CTT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426558 | TTCTTTTTTTTCCCC[-/CTT]CTTCTTCTTCTTTCC | 57091 |
rs371418520 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56422341 | CTGAGAGACCTTTAT[C/T]GTTGCATCATTTCAA | 57091 |
rs371543504 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56449087 | CTAGAAATACCATTT[G/T]CCCCAGCCATCCCAT | 57091 |
rs371583650 | snp | C/T | 0.000484865 | 0.0155627 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452430 | CTCCACCACATCCAC[C/T]GACGACTCCTCCAGC | 57091 |
rs371632873 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56458279 | GCCAAAACAGGAAAG[G/T]GCAGACAGCCACAGC | 57091 |
rs371641786 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56412804 | GTCTGCCTCAGCCCC[C/T]GCTAATTCCTTCTTT | 57091 |
rs371690412 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56426129 | TGATAGAGTCTGTGC[C/T]AAGCAGAGTGGTTTG | 57091 |
rs371714541 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410349 | GAACAAGTAACTGCT[A/G]ATGGGGTAAATGTCC | 57091 |
rs371792476 | snp | A/C/G | 4.97709e-05 | 0.00498833 | synonymous-codon, missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453066 | TACCCCTTCCACTAA[A/C/G]CAAAGGGAAGATGAA | 57091 |
rs371811746 | snp | A/G/T | 8.92155e-05 | 0.00667838 | missense | CASS4 | GRCh38.p7 | 20:56458673 | TACCCCAGCCCTGCC[A/G/T]CGCTGGGGCACCTCC | 57091 |
rs371909048 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420719 | AAGTGAGAGTCTCCC[C/G]ACGGTTGAAAGGGGA | 57091 |
rs371959603 | in-del | -/T | 0.397271 | 0.202018 | intron-variant | CASS4 | GRCh38.p7 | 20:56420556 | ACCATGCCCATCTAA[-/T]TTTTTTTTTTTTTTT | 57091 |
rs372033906 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450088 | CCAGGCTGGAGCACA[A/G]TGGTGCGATCTTGGC | 57091 |
rs372069487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443538 | GGGCTTGTCCACCTA[C/G]ACCAATCAGCCTGAG | 57091 |
rs372082900 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428432 | ACCCAGGCCCCCTGA[C/T]TATTAACGTTGAGTT | 57091 |
rs372142142 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458513 | TCAGAGCAAGCTGGT[C/T]ATCATGGTGGGACAG | 57091 |
rs372147245 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457737 | TTACAAATTTAGCTG[G/T]GTGCAGTGGCTCACC | 57091 |
rs372172040 | snp | A/G/T | 4.94338e-05 | 0.00497141 | synonymous-codon, missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452034 | TCCTCCAAGTGGCAG[A/G/T]TCCAGGTCCCTCACT | 57091 |
rs372207663 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416855 | GCAAGCATCTTTACT[A/G]TGTTACTGAAGAGTG | 57091 |
rs372229859 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417432 | TCTCTGGACCACGCT[A/G]TGCAAATCACTTCCC | 57091 |
rs372323659 | snp | A/G | 0.000338593 | 0.013007 | intron-variant | CASS4 | GRCh38.p7 | 20:56445861 | GTGATCATCAGAGTG[A/G]CATTTCCTTTTCCTC | 57091 |
rs372419278 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452320 | GCGGGCCATAATTCC[C/T]CATGGTTCTCCAGAC | 57091 |
rs372446953 | snp | A/G | 3.29804e-05 | 0.00406068 | missense | CASS4 | GRCh38.p7 | 20:56458398 | CTGAGAGGAAACCCC[A/G]CTTATCTGAACACTG | 57091 |
rs372452210 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417863 | TCCCCCTCCTTGTCC[A/G]TGGTCAGATGTTGCC | 57091 |
rs372552802 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431394 | CATAATTAATTGATT[A/G]CATGAGCTGTCCAGA | 57091 |
rs372619679 | snp | G/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410822 | TATTATTAATATAAT[G/T]TATATCTTAATATCT | 57091 |
rs372643953 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CASS4 | GRCh38.p7 | 20:56450707 | AGGTGCTAAGGTGCG[A/G]TGTTATGAACACACA | 57091 |
rs372663259 | snp | C/T | 0.000197677 | 0.0099398 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451949 | CCAGCGTCAGAAACA[C/T]GCCTCTCACCAGCTT | 57091 |
rs372705649 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436811 | AGGACTGCCTGAGCC[C/T]GGGAGGTCGAGGCTG | 57091 |
rs372836634 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454705 | CCTATCTTGGAATAA[A/T]GGTTAGATGAAAACA | 57091 |
rs372852099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56418773 | ATTTATGTGTGTTAC[A/G]TTTGATTCAGGAACA | 57091 |
rs372994301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56437721 | GCTGGCAATCACGCT[C/T]GGGGAGCTTGTGTGC | 57091 |
rs373081629 | in-del | -/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56453233 | TGTATAGGCTTTGGG[-/G]AGACACTGGTTCCAT | 57091 |
rs373117837 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456536 | CTGCCACCACACCCG[A/G]CTAATTTTTTGTATT | 57091 |
rs373141403 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414958 | TTTTCTCACTATTAC[A/G]TCCTCACAACATCCT | 57091 |
rs373223729 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410560 | CTGGCCAACATGGTG[A/G]AACCCTGTCTCTACT | 57091 |
rs373249903 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444235 | GGACACCATGATGAA[C/T]AGAGGGACCCTGACC | 57091 |
rs373302883 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417676 | GTGAACGAATGGGAG[C/G/T]TTACAGGGAGTGCAG | 57091 |
rs373317345 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56430874 | GAGAAAAGTAAGAAA[A/C]CAATGTGACTGGAGG | 57091 |
rs373353115 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455238 | CATTTTTCACAGTTT[C/T]CTTTAAATTAATGTA | 57091 |
rs373374371 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456511 | CCTGAGTAGCTGGGA[C/T]TACAGGCGCCTGCCA | 57091 |
rs373392977 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456522 | GGGACTACAGGCGCC[C/T]GCCACCACACCCGGC | 57091 |
rs373484879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56435470 | CTTTTATTTCTCTCT[C/T]TTTCTGTAATGAACA | 57091 |
rs373486510 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443659 | AGCATCGTGATGGGA[G/T]GGGGAAAGGCGGGGT | 57091 |
rs373489632 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415362 | ACGCAGTACCAGGAA[A/G]CACCCAAGTTGTCGA | 57091 |
rs373604871 | snp | A/G | 4.1088e-05 | 0.00453236 | missense | CASS4 | GRCh38.p7 | 20:56458722 | TGGAGCAACACACGC[A/G]GCAGTTCAGAGGGAC | 57091 |
rs373633684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413094 | TGTACTCCAGCTACC[A/G]GAGAGGCTGAGGTGA | 57091 |
rs373652454 | snp | A/G | 4.96036e-05 | 0.00497989 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453041 | GAGAAACTGAATCAC[A/G]CCAAAAGAGTACCCC | 57091 |
rs373834332 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411504 | GTGAGCCGAGATTGC[A/G]CCACTGCGCTCCCAC | 57091 |
rs373845833 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416070 | CGTGGGTTTTTTTGA[A/G]GTGGAGTTTCACTCT | 57091 |
rs373856434 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457226 | ATCTGTCTGAATGCT[A/T]CCGGGCTATGAATTT | 57091 |
rs373886757 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56441366 | TCCCAGCAATTTGGG[A/G]GGCCAAGGCGGGTGG | 57091 |
rs373921934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451010 | CCTGTCTCTAATAAA[A/G]TACAAAAATTAAAAA | 57091 |
rs373969722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414754 | TCAGGGGATTAGCCT[A/G]GCCAAAATGGTGAAA | 57091 |
rs374168804 | snp | C/T | 5.82903e-05 | 0.00539831 | missense | CASS4 | GRCh38.p7 | 20:56412487 | GCATCATGGACTGTG[C/T]GCCCAAGGTGAGTGA | 57091 |
rs374225825 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416613 | CTTCATACACAGCCC[G/T]TTTTTCCCCAATAAC | 57091 |
rs374255442 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431372 | CTTTGCTACTGAAAC[A/G]CTGAGGCATAATTAA | 57091 |
rs374334468 | snp | C/T | 1.66518e-05 | 0.00288542 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56437337 | CAACCGCCTCCAAAT[C/T]CTCACGGAGGTCGCT | 57091 |
rs374389367 | snp | A/C | 1.65018e-05 | 0.00287239 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458585 | CGTGCGCAACGAGAT[A/C]CTCCGTGGCAGCAGT | 57091 |
rs374488395 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448832 | AAGGAGTTTGAGCAG[A/G]GGAGTGACAATCAGA | 57091 |
rs374502408 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410322 | AACAGTGGTTTCCAG[A/G]GGCTGGGGGAAGAAC | 57091 |
rs374503819 | snp | A/T | 0.154329 | 0.23097 | intron-variant | CASS4 | GRCh38.p7 | 20:56442666 | GTGCTGGCCTAATTT[A/T]AAAAAAAAACCCACC | 57091 |
rs374506752 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425192 | GGGATAGCAGGAAGG[A/G]CAGCGAGCCTCCCCC | 57091 |
rs374510167 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459658 | TATTTTTAGTAGAGT[C/T]GGGGTTTCACCATAT | 57091 |
rs374578148 | in-del | -/AT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436373 | tgtatatatatatat[-/AT]gtatatatatatata | 57091 |
rs374685259 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443829 | GTCTGAAGCGCTACA[C/T]GAGGGCCTGGGAATC | 57091 |
rs374708945 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441503 | CCAACTACTCAGAAG[A/G]CTGAGGCAGGAGAAT | 57091 |
rs374783665 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438537 | GAGGGAAGAAAGATC[A/T]ATTTAAACAAAAACC | 57091 |
rs374794797 | snp | G/T | 1.64773e-05 | 0.00287026 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458543 | GAAGCTGGTGGACAC[G/T]CTGTGCATGGAGACC | 57091 |
rs374797932 | snp | A/G | 1.84831e-05 | 0.00303993 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458693 | GGGGCACCTCCAGGC[A/G]GAGGCTGAGAAGCTG | 57091 |
rs374807005 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418835 | GAATGCCTGCTGCAC[A/G]CCAGGCACTGTTCTA | 57091 |
rs374826702 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419140 | GTTTTGGAATTGCGA[C/T]GACTAAGGGAGGAAA | 57091 |
rs374839476 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454859 | GGCGAGAGTTCGTTT[C/T]TGTGATTCTTTGTCC | 57091 |
rs374846856 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418528 | CTGCTGTGCAACAGA[C/T]GGGCTGTAAGTAGGA | 57091 |
rs374955001 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434938 | CACTGCAGGCATTTT[A/T]ATTTTCTTCTGTTTG | 57091 |
rs374978146 | snp | A/G | 0.000166193 | 0.00911421 | missense | CASS4 | GRCh38.p7 | 20:56437272 | CACGTGCCAGAAAGC[A/G]AGGGTTGGTGGAAGT | 57091 |
rs374995714 | snp | A/G | 3.31345e-05 | 0.00407016 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451856 | CAGTGACTACCTTAA[A/G]AAGAGGCGGTTACAG | 57091 |
rs375006912 | snp | A/G | 3.29489e-05 | 0.00405874 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56451950 | CAGCGTCAGAAACAC[A/G]CCTCTCACCAGCTTT | 57091 |
rs375037401 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56429654 | CGCCCCCTCACCCAC[A/G]CACTCCGGCCTCCAC | 57091 |
rs375060406 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56443471 | GAGACTCCGTCTCCA[A/G]AAAAAAAAAGAAGCT | 57091 |
rs375068966 | snp | A/G | 3.29489e-05 | 0.00405874 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458432 | GCTCTACTTTGGGGC[A/G]CTCTTCAAAGCCATC | 57091 |
rs375070353 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56425981 | CCCGTTTCCATTGAC[A/G]TAAGCTCTACCTCAT | 57091 |
rs375093835 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427403 | TTTTTAACATAATAT[C/T]CTTTTAAAATGATGG | 57091 |
rs375097014 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56449341 | GGAAACCATCATTCT[G/T]CACAAACTATTGCAA | 57091 |
rs375138344 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410803 | TAATATAATATTAAT[A/G]TATTATTATTAATAT | 57091 |
rs375199170 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418121 | GGAGTGAGCATGACA[A/G]TGAGTAAATAGACCC | 57091 |
rs375202883 | in-del | -/A | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56438302 | TCAAAAAAAAAAAAA[-/A]GTATATCCCCTTCAA | 57091 |
rs375221341 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420766 | CAGTAATCAATAACA[A/G]ACAACTCAAGGTGCT | 57091 |
rs375230437 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442862 | TTCCTTAACTGATTG[C/T]CATACTGGGCCTACG | 57091 |
rs375252435 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450045 | TCTTTTTTTTTTTTT[C/T]TTTGAGATGGAGTTT | 57091 |
rs375291893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442521 | CAGCTCTGTAACTTA[C/T]ATCCAGACCACGAAA | 57091 |
rs375377797 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454696 | AAAGATAAACCTATC[C/T]TGGAATAAAGGTTAG | 57091 |
rs375384896 | snp | C/G | 0.000117804 | 0.00767387 | intron-variant | CASS4 | GRCh38.p7 | 20:56445886 | TTCCTCTTTTCTCCT[C/G]CTTTCTCTCCAAGGC | 57091 |
rs375413281 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456518 | AGCTGGGACTACAGG[C/T]GCCTGCCACCACACC | 57091 |
rs375458336 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417613 | TCTCCGGTGCCTACA[A/G]CAGTGCCTGCACAAA | 57091 |
rs375617715 | microsatellite | (CA)11/12/13/14/15 | 0.645984 | 0.195214 | intron-variant | CASS4 | GRCh38.p7 | 20:56416530 | CATGTGTGCATACAA[(CA)11/12/13/14/15]GGAAGAAACAGAATT | 57091 |
rs375619279 | snp | C/G | 0.000153988 | 0.00877328 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452447 | ACGACTCCTCCAGCT[C/G]TTCCTCGGAGGAGTC | 57091 |
rs375637319 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415753 | TCGCCTTTGTACATC[A/G]TATGGTAAACAGGGA | 57091 |
rs375670350 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448513 | ATACAACTCAAGTCA[C/T]TGAATGGTCCCATGG | 57091 |
rs375769297 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409640 | TCAGAAAAGAAAATT[C/T]GGTCCAAACTACTGT | 57091 |
rs375835691 | snp | C/G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418701 | CGCTGGTCGCCGTGT[C/G/T]GGGTGGGGAGTGGTT | 57091 |
rs375881405 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411047 | CAGACTTGTGGGGAC[A/G]ACACATGGGACAACC | 57091 |
rs375961803 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416317 | AGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG | 57091 |
rs376026138 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56456749 | AGTGGTGAGATCATG[A/G]CTCACTGCAGCCTCC | 57091 |
rs376063661 | snp | C/T | 3.72225e-05 | 0.00431391 | intron-variant, synonymous-codon | CASS4 | GRCh38.p7 | 20:56437547 | CCCTCCCACCAGTGC[C/T]AGAATCATCTGTGAA | 57091 |
rs376133919 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417026 | AAGGATCAAGGTAAA[A/G]ATGTAGAATTTTTTA | 57091 |
rs376146986 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420290 | GGGTTAGGGAGGGAC[A/G]GGGGGCAAAAGAGCA | 57091 |
rs376413844 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417686 | GGGAGCTTACAGGGA[A/G]TGCAGGTGGAGCCCT | 57091 |
rs376416362 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438462 | GGTTATACATATCTT[A/G]GCATATCACCACAAC | 57091 |
rs376422994 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414066 | ATTCATCTACAGAAC[A/G]TAGAAGAATATCTAC | 57091 |
rs376478767 | snp | C/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409740 | ACTCCAGCTGTTTCA[C/G]CCTTCAGACAACCGG | 57091 |
rs376483191 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444900 | CAGATCACCTAAGGT[C/T]GGGAGTTCAAGACCA | 57091 |
rs376536924 | snp | C/G/T | 0.000200236 | 0.0100041 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458767 | TGTCTACCTCCCTTC[C/G/T]TCCTCTGCTCACCTC | 57091 |
rs376637024 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418608 | TTCCACTGGGGTGGT[A/G]CCCTGCTCTTCTCCA | 57091 |
rs376664080 | snp | C/T | 3.35841e-05 | 0.00409767 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458648 | GGCCACTAAGAATGC[C/T]GTGCTCACGTACCCC | 57091 |
rs376709280 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417105 | GGCTTGGAAGTGTGT[A/G]CCACTTGCTGGGACT | 57091 |
rs376715177 | snp | C/T | 1.66941e-05 | 0.00288908 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452421 | TTCCTCGTGCTCCAC[C/T]ACATCCACCGACGAC | 57091 |
rs376814976 | snp | A/C/G | 4.95441e-05 | 0.00497694 | synonymous-codon, missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452566 | ATGCTCTTTGTCAGC[A/C/G]GGAAGTGGAGATTCC | 57091 |
rs376819122 | snp | A/T | 6.59283e-05 | 0.00574106 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452059 | CTCACTCCACAACTG[A/T]ATAACAATGTGCCCA | 57091 |
rs376902758 | snp | A/T | 1.75597e-05 | 0.00296303 | intron-variant | CASS4 | GRCh38.p7 | 20:56450718 | TGCGGTGTTATGAAC[A/T]CACAAAATCCTCTCA | 57091 |
rs376949340 | snp | C/T | 1.66674e-05 | 0.00288676 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452355 | AACTTCCCCATCTCC[C/T]GAACCGGACAGATTA | 57091 |
rs377023136 | snp | C/T | 0.000165777 | 0.0091028 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56453063 | GAGTACCCCTTCCAC[C/T]AAGCAAAGGGAAGAT | 57091 |
rs377055209 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409811 | GCAATGTTTGTCCAC[A/G]TTAAAGGCTCATTTG | 57091 |
rs377068009 | snp | C/T | 1.7849e-05 | 0.00298734 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56437211 | CCCTGACTGCTCTGA[C/T]GAGCTGGCTTTCAGC | 57091 |
rs377131087 | snp | A/T | 2.45631e-05 | 0.00350442 | stop-lost | CASS4 | GRCh38.p7 | 20:56458745 | AGAGGGACACTGGGA[A/T]GAGGACTGTCTACCT | 57091 |
rs377289897 | snp | C/G | 4.97352e-05 | 0.00498649 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452233 | AATATTTATGACATC[C/G]CTAAAGCAACGTCGA | 57091 |
rs377363864 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427173 | AAGACCCTGTCTCTT[-/A]AAAAAAAAAAAAAAA | 57091 |
rs377418666 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444404 | CCCTGTCCTGGACTC[C/T]GGAGCTTCACCCTGT | 57091 |
rs377432827 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428110 | CCTTCCCAAAGAAAG[A/G]ATGATATTCTAGGTT | 57091 |
rs377435787 | snp | A/G | | | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459053 | ATTAAATGTGTGCAT[A/G]TTTTGTTTGTTTTTT | 57091 |
rs377529791 | snp | C/G | 0.00011533 | 0.00759287 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458534 | GGTGGGACAGAAGCT[C/G]GTGGACACGCTGTGC | 57091 |
rs377548034 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456523 | GGACTACAGGCGCCT[A/G]CCACCACACCCGGCT | 57091 |
rs377626151 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411518 | CGCCACTGCGCTCCC[A/G]CCTGAGTGACAGAGA | 57091 |
rs377658343 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447036 | AACATGGTGAAACCC[C/T]GTCTCTCCTAAAAAT | 57091 |
rs377672811 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409896 | TCATTCAGAAAAACC[A/G]TAGAGGGCTCAAATA | 57091 |
rs377677159 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424196 | AAATATTTCTGATAA[A/T]GAGATGCAGATTATT | 57091 |
rs377729881 | snp | A/T | 3.29516e-05 | 0.00405891 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452740 | CGGGACCAGATGCAG[A/T]CCATCTCCAACTCCT | 57091 |
rs377756269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56441374 | ATTTGGGAGGCCAAG[A/G]CGGGTGGATCACCTG | 57091 |
rs386815434 | in-del | AA/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438301 | TTCAAAAAAAAAAAA[AA/G]GTATATCCCCTTCAA | 57091 |
rs386815435 | multinucleotide-polymorphism | GGA/TGG | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441364 | AATCCCAGCAATTTG[GGA/TGG]GGCCAAGGCGGGTGG | 57091 |
rs386815436 | in-del | CAAATAAGTGAGAGCTGGGAGGGAGGAGACA/TCTGGGAGGTACCAC | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443091 | AAAGCTTGGTGTGTT[lengthTooLong]TGGCGGTACAGCCAG | 57091 |
rs397715320 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456094 | ACTTGGAAAGCCCCC[-/C]GCTTTAGACTGACAG | 57091 |
rs397755281 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447220 | TGAAAAAAAAAAAAA[-/A]TCAAAATCAAAAATT | 57091 |
rs397812549 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438441 | ATGTTTATTAACAGT[-/T]GGATTGGTTATACAT | 57091 |
rs397865375 | in-del | -/AA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448157 | AAAAAAAAAAAAAAA[-/AA]TAGTTATCAATGAAG | 57091 |
rs397961510 | in-del | -/GT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416558 | TGTGTGTGTGTGTGT[-/GT]ATGCACACATGCCAT | 57091 |
rs397966056 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56446023 | TTGTTCAGGGGCCCC[-/C]TCATCACCCAGACCT | 57091 |
rs397970295 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419539 | TAAGTGATCCTCCCA[-/A]CCTCAGCCTCCCAAG | 57091 |
rs398040797 | in-del | -/T | 0.5 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56456391 | CTTCTTTTTTTTTTT[-/T]GAGACGAAGTCTTGC | 57091 |
rs398081415 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447219 | CTGAAAAAAAAAAAA[-/A]ATCAAAATCAAAAAT | 57091 |
rs398088524 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56451508 | AAAAGAAAGGGTTGC[-/C]AAGGGCATTTAGAGC | 57091 |
rs398088525 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457773 | AATCCCAGCACTTTA[-/A]GGAGGCTGAGGTGGG | 57091 |
rs398101461 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447858 | GTGTAAAAGTTATCA[-/A]TGGGCCGGGCGCGGT | 57091 |
rs527243942 | in-del | -/C | 0.128976 | 0.218754 | intron-variant | CASS4 | GRCh38.p7 | 20:56442676 | AATTTAAAAAAAAAA[-/C]CCACCACATCAAGAG | 57091 |
rs527320120 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428763 | GGAAAGGCCGTGCAG[A/C]GTATTGGCAATAGCA | 57091 |
rs527330431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445695 | AACATCGTGGGCCAC[A/G]TGCGAGGAAGGCTGC | 57091 |
rs527331123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438654 | ACAAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 57091 |
rs527370269 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432623 | TCCACACGCTTTGGC[C/T]TCCCAAAATGCTGGG | 57091 |
rs527392465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56439224 | CCCAGGCTGGAATGC[A/G]GTGGTGCAATCACTG | 57091 |
rs527480200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56456137 | GAGGCCCGGGGCACC[A/G]TTGGCCACCGGGTGG | 57091 |
rs527486794 | snp | C/T | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56418066 | ATAGTTATTGGGCTC[C/T]GGGGGTTCAGGGTGA | 57091 |
rs527489175 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411151 | TAAAAAATTAAAAAA[C/T]GCTGTCTGACAAGAA | 57091 |
rs527600923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451009 | CCCTGTCTCTAATAA[A/C]ATACAAAAATTAAAA | 57091 |
rs527682620 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56457975 | AGCTGAGATTGCACC[A/G]TTGCACTCCAGCCTG | 57091 |
rs527690178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413065 | GAAAGAAGCCAGGCA[C/T]GGTGGTACATACCTG | 57091 |
rs527804312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446284 | CTTGTTGAGATGGGG[G/T]CTTGCTTTGTTGACC | 57091 |
rs527807357 | snp | A/C/T | 1.65655e-05 | 0.00287793 | missense, synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452548 | AGCTCTGTCGCTGGC[A/C/T]TGATGCTCTTTGTCA | 57091 |
rs527922839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56425902 | ATACTTATAAAAGCA[C/T]CAATGCAGACCTATG | 57091 |
rs527956104 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56418948 | ACTCATTATTGGTTC[C/T]CCTGTTTAATCACCT | 57091 |
rs527986867 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56426328 | ATATCAAATGCGGTC[A/T]TCAGTGCTGACTGCT | 57091 |
rs528029092 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434891 | GGAAACACAAAAACC[A/G]AAGGATTAACAGCAG | 57091 |
rs528095779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447582 | CCTGTAAGTGCCCCC[C/T]ACCTCCTACCCCTCA | 57091 |
rs528206656 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459345 | CAATTCTCCAGAGAG[C/T]GGTGACATTTTCAGC | 57091 |
rs528258611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56440284 | TCTGAGCAGCTGACT[C/T]GGAGCAGAGCTTTGC | 57091 |
rs528335328 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56441084 | ACCTCTGCCTCCTGG[G/T]TTCAAGAGATTCTCC | 57091 |
rs528361899 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440001 | CTACTCACCATTCAG[G/T]CCTTCTCCACACCAG | 57091 |
rs528451703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56442581 | GTGCCTTCTCTCTGT[C/T]ACTTCCCCACTAGGG | 57091 |
rs528514246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56436032 | GCTGGGATTACAGGC[A/G]TGAAACACTGCGCCC | 57091 |
rs528588935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56436699 | GTTGGAAACCAGCCT[A/G]GGCAATGGCAAAACC | 57091 |
rs528642551 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56453293 | AATTCTTGATGAAAT[C/G]TTATTAACAAGTCAG | 57091 |
rs528651720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414679 | AGATAGGCCGGGAGC[A/G]GTGGCTCATGCCTGT | 57091 |
rs528680035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56415456 | CATCTATAAGATACA[C/T]GTTTTAAGGTTTTAC | 57091 |
rs528700817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447623 | GAGCATCTCTTACCT[C/G]CAAGTCCCTCCAGGT | 57091 |
rs528887840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56434054 | ACAAAGATTTCTAAA[A/C]AAATACATCATCCAA | 57091 |
rs528976085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56427450 | AGCCAACAGATAATA[C/T]CCTTCTCTCTGCATT | 57091 |
rs529061432 | snp | C/T | 0.000299795 | 0.0122396 | intron-variant | CASS4 | GRCh38.p7 | 20:56445893 | TTTCTCCTCCTTTCT[C/T]TCCAAGGCCATCCTC | 57091 |
rs529062258 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56451389 | ATTGGATTCTACCAC[-/AT]GTGTCCCACAGACAC | 57091 |
rs529099912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56439561 | GGCACCTATAGTCCC[A/G]GCTACTCAGGAGGCT | 57091 |
rs529133273 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56446153 | CAGAGGCCAACTTCA[C/T]AACCTCCTTTTTACC | 57091 |
rs529159751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56440199 | CTTCTGAAGCAGTCA[A/G]TGAGGTGGACACTAA | 57091 |
rs529230816 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410131 | GGAAGAATCACTGCC[A/G]GGAGTCTGCCAAGTT | 57091 |
rs529267086 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443392 | GAGAATCGCTTGAAC[C/T]CGGGAGGTGGAGGTT | 57091 |
rs529307019 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413566 | TGATCCCAGCTACTC[A/G]GGAGGCTGAGGCACA | 57091 |
rs529362350 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416270 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 57091 |
rs529507123 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458972 | TAAAGACCTTGTGAA[A/G]TTTAGCATATATGGA | 57091 |
rs529518563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413841 | AAAAATATGGGAAGC[A/G]TGGGGGTTATTCAGT | 57091 |
rs529524026 | snp | C/T | 3.29533e-05 | 0.00405901 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452758 | ATCTCCAACTCCTAC[C/T]GCATCCTGCTTGAAA | 57091 |
rs529554289 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435162 | AGTGTTTCCCCTAAT[C/T]CACACAGACCTGCTT | 57091 |
rs529606208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414669 | AATATTATACAGATA[G/T]GCCGGGAGCGGTGGC | 57091 |
rs529610945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56415544 | TACGTACTGGTGTTC[A/G]GTTCATATTAGTGCA | 57091 |
rs529615536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56453219 | GACTCTTTCCATAGT[A/G]TATAGGCTTTGGGGA | 57091 |
rs529709132 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56454304 | GCCCAGAAGTCACTT[G/T]GGGGCTGTGTCAAGG | 57091 |
rs529770734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56454836 | ACATTACAGCCATGA[A/C]CCACATGGGCGAGAG | 57091 |
rs529771677 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409839 | TTGCCTTAAAATACT[A/G]ATGGATTGCAGCAAA | 57091 |
rs529821062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56449160 | AAGATACATGCACAC[A/G]TATGTTTATTGCGGC | 57091 |
rs529971106 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56458071 | CCAATGTGTTTCTTA[A/G]AATGGGTTTCTTGTA | 57091 |
rs529980727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56421838 | TTTCCTTAAAAAAAG[A/G]AAAAAGGAAAGAGGG | 57091 |
rs530006173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56437745 | TGTGTGCCAGGTTGG[G/T]ATGGAGAACTCAGCG | 57091 |
rs530069192 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56431116 | CCAATTAGAATTTAA[A/G]TGACCTTGGACAAGT | 57091 |
rs530117301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424429 | GCCACTGCAATTCAT[A/G]GGGGAAAAGAAAAGT | 57091 |
rs530148852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56423737 | TTTAGTAGAGTCGGG[A/G]TTTCACCATGTTGGC | 57091 |
rs530275070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443973 | AAGTTTCTCAGGGAG[C/T]AAGAAAGCAGTCGTC | 57091 |
rs530279249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56436909 | AAAACAAACAGGGCC[A/G]TGAAAGCATATTAGG | 57091 |
rs530300603 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56443464 | ACAGAGCGAGACTCC[A/G]TCTCCAAAAAAAAAA | 57091 |
rs530332234 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56451749 | CGGAGTGACGATGAG[A/T]TTTAAACAACGCACT | 57091 |
rs530351558 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56423024 | AGCCCATCCTTCCCC[A/G/T]TGGCTGGGGTGGCAG | 57091 |
rs530379166 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56429155 | AGCTGCTTCTCTCCC[A/G]GCTCATCTAAGCTGC | 57091 |
rs530414283 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459431 | ATGTGCAATTCCTTA[C/T]AGGGCTAGCTTGGTT | 57091 |
rs530427713 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417321 | ATTAGATCCCACTCC[A/C/G]AGCAGCTCTCCTGCC | 57091 |
rs530434016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421757 | TTCTAATTGGTGTCG[A/G]CATAATTGCTTACGA | 57091 |
rs530518779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56415489 | AAATAGGAGCTGTAA[A/G]TAAAGATCTGTTGAG | 57091 |
rs530900641 | in-del | -/A | 0.37138 | 0.218556 | intron-variant | CASS4 | GRCh38.p7 | 20:56427174 | AAGACCCTGTCTCTT[-/A]AAAAAAAAAAAAAAA | 57091 |
rs530900974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56430548 | TCAGCAACCATTGCA[A/G]TGGTTACTGGATGCC | 57091 |
rs531219703 | snp | C/G | | | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452086 | CCCATGCAGAAAAAA[C/G]TCAGCCTTCCAGAAA | 57091 |
rs531257470 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455651 | ACTCACATGGCTGGC[C/T]GGGCATGGTGGCTCA | 57091 |
rs531546654 | in-del | -/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56446388 | AAGCCACCGTGCCCA[-/G]CCATTATTTATAATA | 57091 |
rs531568277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56418310 | CAGCATAGTACAGGG[C/T]CCCTGTAAAGACCCA | 57091 |
rs531596249 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416938 | TTTTAAATTCAGCCT[A/C/T]AATTAAAGAGCAAAT | 57091 |
rs531603935 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411836 | GCATGGGGTTCCGAG[C/T]AGGGTGAATGCACAA | 57091 |
rs531633598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417465 | CTACACAGGCCCACC[A/G]CCAACACTCTCATCT | 57091 |
rs531655524 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56450048 | TTTTTTTTTTTTCTT[G/T]GAGATGGAGTTTCGC | 57091 |
rs531687087 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CASS4 | GRCh38.p7 | 20:56425843 | CCCTGTTTCCTACCC[A/C]GAAGGGACCCTCAGT | 57091 |
rs531749035 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436364 | TGTGTGTGTGTGTAT[A/G]TATATATATGTATAT | 57091 |
rs531765765 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56419222 | GTAAGAGAGCTGCCA[C/T]GGAGGGGGAGATTAG | 57091 |
rs531841723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56432045 | ATAGGGAATCAATGA[A/G]ATGTTAAAACTAGGT | 57091 |
rs531908816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438582 | TCAAAAAAGAGGCAG[A/G]GCGCAATGGCTCATT | 57091 |
rs531975802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416852 | CAAGCAAGCATCTTT[A/G]CTATGTTACTGAAGA | 57091 |
rs531998067 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447081 | GGCATGGTGGTTCAC[A/G]CCTGTAGTCCCAGCT | 57091 |
rs532183915 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56449960 | ATGAACTCAAGATAA[A/T]TTACCATTTTTAATT | 57091 |
rs532250162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450414 | CCTGCGTTGCCTCAG[A/G]CAAGGAAGGCGGGAG | 57091 |
rs532382976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56425177 | AGTTCAAGGATCACT[A/G]GGATAGCAGGAAGGG | 57091 |
rs532424129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56423418 | CAAATGACTGTCACA[C/T]CATGGGAAACAATTG | 57091 |
rs532467386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56454954 | TGAAGCATTAACCAT[C/T]ACTGAAATGACTGTA | 57091 |
rs532534430 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411798 | TTATTCATTAGGTAC[C/T]ATGAGCAAAGACCAG | 57091 |
rs532551381 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417612 | ATCTCCGGTGCCTAC[A/C]ACAGTGCCTGCACAA | 57091 |
rs532623137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56437848 | TGTGGGAAATGGAAT[A/G]CTTAGCTGAGCTGTG | 57091 |
rs532710700 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454738 | GACTTAGGAACCATG[A/G]TAAGCTATAGCACTC | 57091 |
rs532755789 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56439418 | GCTCATTCCTGTAAT[A/C]CCAGCAGTTTGGGAG | 57091 |
rs532874428 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56431112 | GAACCAATTAGAATT[-/G]TAAGTGACCTTGGAC | 57091 |
rs532937065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451130 | AAAACCTCTCATTGC[A/G]CTTGTGTTCAGGAAT | 57091 |
rs532953288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413093 | CTGTACTCCAGCTAC[C/T]GGAGAGGCTGAGGTG | 57091 |
rs532989671 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415916 | TTTATAGAACAAGGC[A/G]AAATTTTTTTAAAAC | 57091 |
rs533001811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451475 | TGTCAGGGGGATGCA[C/T]AGGGGTTTGGTGGAT | 57091 |
rs533002852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445375 | GACAAGTCCTTAGAC[A/G]GCTCTCAGACCTCAG | 57091 |
rs533037147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433258 | CCTTTTTCTAAGGAA[A/G]TGACATTTAAGATAA | 57091 |
rs533057836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445750 | TGCCCTGCTGTCTTG[A/T]GAGTGAAGAGCCTGC | 57091 |
rs533185309 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443996 | CAGTCGTCACTCAAC[G/T]AAGGGGGCTGTTTTG | 57091 |
rs533336238 | snp | A/C/T | 0.00116938 | 0.0241565 | synonymous-codon, missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452725 | CTTCAGAACAGAATT[A/C/T]GGGACCAGATGCAGA | 57091 |
rs533389215 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432671 | TCACACCCAGCCTAA[G/T]TCTTGACCTTTAATC | 57091 |
rs533409124 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56446790 | AGGTCTAGATGGGGC[C/G]CAAACATCAGGATTT | 57091 |
rs533417197 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442877 | CCATACTGGGCCTAC[A/G]TTTTCCAAGAAGCAC | 57091 |
rs533460142 | in-del | -/ATTT | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56413918 | GTCATATTTGTGTGC[-/ATTT]ATTTGTGTATATTTA | 57091 |
rs533508488 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418197 | GGATCTGATGGAGGC[A/G]ATGGATGGAAAAGGC | 57091 |
rs533516388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56426438 | TGACACAGTTCCTGC[A/G]TAGTTAGAGTGCGAC | 57091 |
rs533569711 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CASS4 | GRCh38.p7 | 20:56437030 | AGAGCAGGGACAAGA[C/G]CCTCTGGGGTGGAAG | 57091 |
rs533661394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424678 | CCCAGGTGGCAGAGG[A/T]TGCAGTGAGCAGAGA | 57091 |
rs533666284 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CASS4 | GRCh38.p7 | 20:56420178 | TGTTAGTGAATGTAT[C/T]GTTCTTTTCCTTTGA | 57091 |
rs533677918 | in-del | -/C | 0.00716266 | 0.059414 | intron-variant | CASS4 | GRCh38.p7 | 20:56435753 | TAGTTTTTCTTTTTT[-/C]TTTTGTTTTGTTTTT | 57091 |
rs533754016 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56438063 | GGGGGGACGAGACAG[A/G]AGGATCATTTGAACT | 57091 |
rs533755957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56430877 | AAAAGTAAGAAAACA[A/G]TGTGACTGGAGGGAA | 57091 |
rs533806495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56444283 | TCCTCTGCCTGCGTT[C/T]CCCTCCCTCAGCTCT | 57091 |
rs533809119 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424098 | TTGCTAAGTTTTTTT[A/T]AAACAGCTCCAAGAG | 57091 |
rs533820322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56431443 | AATGAAACGCCATAC[A/G]GTGTTTCATTCATAT | 57091 |
rs533930812 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436287 | CCTGTACATGACAGA[A/G]AGAGAGATACCCATA | 57091 |
rs533942795 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410236 | CTTTACTCTGTGACC[C/T]TGGGCAAGTTTATCC | 57091 |
rs534029324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56432593 | GGCTGGTCTGGAACT[C/T]CTGGCTTCAAGTCAT | 57091 |
rs534084611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417875 | TCCATGGTCAGATGT[G/T]GCCTTAGATGCAAGC | 57091 |
rs534129404 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447359 | AGCTTGGGCCTGCCT[A/G]CTGGGCTGGGCTCCA | 57091 |
rs534163190 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411316 | TTTTGAGAGGCTGAG[A/G]TGGGTGGATCACTTG | 57091 |
rs534198992 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411965 | GAAGAAATGCTGACC[A/G]CTATCAGAAATTTGG | 57091 |
rs534219150 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429750 | CTAACTCCTCCTTAC[C/G]CCCAGATGGAAGCTT | 57091 |
rs534376644 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56425435 | GAAACCACTCAAGCA[A/C]CTTTCAGCATCCTCC | 57091 |
rs534377125 | snp | A/G | 0.000399281 | 0.0141238 | missense | CASS4 | GRCh38.p7 | 20:56458625 | AGCCTGCTCAAGGAC[A/G]TAGCGCTGGCCACTA | 57091 |
rs534428950 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452809 | CGCAATTGGCCTCTG[A/G]AAGTTCTTGTGACTG | 57091 |
rs534434163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446453 | ACATTTTTTTAAATG[A/G]TATTTTGAAGGATAT | 57091 |
rs534444042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56418413 | AGGGCCTGGTCGGCC[A/G]TGTAAGAGCTTTGAA | 57091 |
rs534447718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456779 | CACCACCCAGGTTCA[A/G]TCGATTCTCCCACCT | 57091 |
rs534496267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433009 | ATGGGGGCGTTATGT[A/C]ACGCCTCTCTTTCAT | 57091 |
rs534556363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56426108 | TAAGATGTCCACACC[A/G]TCTTGTGATAGAGTC | 57091 |
rs534626038 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56419286 | ACATTTTTTAGGAAC[C/T]ATTTCCAAACATAAC | 57091 |
rs534866219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447005 | TTGACACTAGGAGTT[C/T]GAGACCAGCCCAGCC | 57091 |
rs534979272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56428264 | GATGGGGCCATGATG[C/T]TGCCCTGACCCCTGT | 57091 |
rs535001688 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456538 | GCCACCACACCCGGC[C/T]AATTTTTTGTATTTT | 57091 |
rs535009432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56442107 | TCACAGGCTTGGAAC[A/G]CAGCCTTTGTGAGGC | 57091 |
rs535085185 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445243 | CCTCCTCCCCTCCCT[C/T]GCTCCTCTCCATCAC | 57091 |
rs535336452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56432498 | TCAGCCTCCCCAGTA[A/G]CTGGGACTATAGGCG | 57091 |
rs535382764 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439143 | TCATATTGAACATGT[A/T]TGACATCTGTAACTT | 57091 |
rs535392725 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56425576 | TGCTTTTGGCCAAGA[A/T]TAAGATGGACTCAAA | 57091 |
rs535399670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56426025 | ACATTGTACTCCATT[A/G]TACAAATGTCTCCGT | 57091 |
rs535448637 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447865 | AGTTATCAATGGGCC[A/G]GGCGCGGTGGCTCAC | 57091 |
rs535486512 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417844 | CCTGTTCTCTTGACA[A/G]TTGTCCCCCTCCTTG | 57091 |
rs535523849 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56412764 | CATCATTTTGCGTCC[A/T]GCAAACTCCTGAAGC | 57091 |
rs535832095 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56441364 | AATCCCAGCAATTTG[G/T]GAGGCCAAGGCGGGT | 57091 |
rs535835859 | snp | A/G | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56433483 | TTGGGCTTTGTCCAA[A/G]GGGTAATAGGGAGCC | 57091 |
rs535897035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56434275 | ATTAGCTATAAAGAT[A/G]ATCATTTCAGCATTG | 57091 |
rs535928266 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56448511 | GGATACAACTCAAGT[A/C]ATTGAATGGTCCCAT | 57091 |
rs536103563 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441155 | CACCACGCCTGGCTA[A/C]ATTTTTTTTGTATTT | 57091 |
rs536119786 | snp | A/C/G | 0.00199529 | 0.0315338 | intron-variant | CASS4 | GRCh38.p7 | 20:56414900 | TAGCCAACCCTTACC[A/C/G]ATTGTCTACATGTGA | 57091 |
rs536126976 | snp | C/T | 1.65002e-05 | 0.00287225 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452998 | AATGCAGAATTTAAG[C/T]GTGAAAAATACATCC | 57091 |
rs536159662 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444062 | GTTCATCCTGTTCGC[A/G]TTGCGGCTGCTTTGT | 57091 |
rs536166322 | snp | C/T | | | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452814 | TTGGCCTCTGGAAGT[C/T]CTTGTGACTGACAGT | 57091 |
rs536205262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56422891 | ATATCCAAGTTCACC[C/T]GGTTCATTCACTTCT | 57091 |
rs536242810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447911 | ACTTTGGGAGGCTGA[A/G]GCAGGTAGATCACGA | 57091 |
rs536299815 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56455093 | ATTTGGGGCTTGTAT[A/G]TCTTCAACACCTCTT | 57091 |
rs536304402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442289 | GTGCGATCTCTGCAT[A/G]TCTTTAGATTAGAAC | 57091 |
rs536379502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56455850 | GCAGGAGAATTGCTT[C/G]AACCCGGAAAGCAGA | 57091 |
rs536400581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420545 | TGGTGCACGCCACCA[G/T]GCCCATCTAATTTTT | 57091 |
rs536434763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56436330 | ATATAATGGATTGCT[A/G]TATATATGTGTGTGT | 57091 |
rs536463759 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56425854 | ACCCAGAAGGGACCC[C/T]CAGTGAGTGACATAA | 57091 |
rs536466343 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56456136 | GGAGGCCCGGGGCAC[C/T]GTTGGCCACCGGGTG | 57091 |
rs536496336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56429600 | CCAACTTTCCATGCG[C/T]CCCCAACACATACAT | 57091 |
rs536522768 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459444 | TATAGGGCTAGCTTG[A/G]TTCTTCTTCAATGTC | 57091 |
rs536583601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56453596 | AGCTACTCTTAGAAA[C/T]ACTTTTCTGAGGCTG | 57091 |
rs536600638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56415910 | AATTGTTTTATAGAA[C/T]AAGGCGAAATTTTTT | 57091 |
rs536708675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56447138 | ACTTGAACCTGGAAG[A/G]TGGAGGTTGCAATGA | 57091 |
rs536769933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56441432 | CAACATAGTGAAACC[C/T]TGTCTCTACTAAAAA | 57091 |
rs536787548 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56449374 | ACAGAAAACCAAACA[A/C]CGCATGTTCTCACTC | 57091 |
rs536877576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56427735 | TGTGATATTTATAGT[A/C]TATGCAGTTTTTAAA | 57091 |
rs537022356 | in-del | -/CTGA | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56433627 | TGAAGGAACAATTGG[-/CTGA]CTGACCCAGAAAGAC | 57091 |
rs537065117 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435837 | CTCATTGCAACCTCC[A/G]CCTCCAGGGTTCAAG | 57091 |
rs537399314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421345 | TTACCTAAAAAATTG[C/T]AGTGGCACGTGGATA | 57091 |
rs537464771 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420935 | TATTAACAACTAAAC[A/G]AACAAACCTAGTGAA | 57091 |
rs537487242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56422125 | AGCCCCTTGACTTGA[C/T]CCAACAGTTCCCCAA | 57091 |
rs537542321 | snp | A/G | 0.289683 | 0.24683 | intron-variant | CASS4 | GRCh38.p7 | 20:56413185 | TAAAAAAAAAAAAAA[A/G]AAAAGAAAAGTTAAA | 57091 |
rs537587903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56454452 | ACTTTAAACAAACCA[C/T]GTGGGTCATTATATC | 57091 |
rs537597566 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56430903 | GGGAAATGAATGAGG[G/T]TAGAGCTGCAAACTG | 57091 |
rs537642487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56455004 | GTGGGTGGTACTGAC[A/G]GGGCTAAATAGGACT | 57091 |
rs537693098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56435282 | TCAACAAACATAATG[C/G]AAGAGTTGGTCACTT | 57091 |
rs537708194 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56449302 | CGATGAGTTCATGTC[C/G]TTTGTAGGAACATGG | 57091 |
rs537818844 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411263 | ATAAAAATGCAGGCC[A/G]GGGCCAGGCGTTGTG | 57091 |
rs537886051 | snp | C/T | 1.70699e-05 | 0.00292142 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437458 | CCTCCCACTCCAGGC[C/T]CCGTTTATGAGCAGA | 57091 |
rs537905542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444919 | AGTTCAAGACCAGCC[C/T]GACCAATATGGTGAA | 57091 |
rs538010096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56423810 | TCGGCGTCCCAAAGT[A/G]TTGGGATTACAGACA | 57091 |
rs538010374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416281 | TCTCGAACTCCTGAC[A/C]TCAAGTTATCTGCCT | 57091 |
rs538039959 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56448577 | GGCAACCCCCGCTAC[A/G]CCGCACCCCATTTCC | 57091 |
rs538092998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417232 | GAGGTGGTGAGCAAG[A/G]CATTTCAAACTCAGT | 57091 |
rs538128174 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410707 | TTACACCACTGCACT[C/T]CAGCCTGGTGACAGA | 57091 |
rs538130215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417763 | AGCAGGTGTTTGGCA[A/G]CGGAGGTCATTCCTG | 57091 |
rs538181851 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56432025 | TAATCAATTTTGATC[-/A]ATTAATAGGGAATCA | 57091 |
rs538227395 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56422248 | CGATCTCTGGAGCAC[-/T]TTTGAGTTGGAGAAT | 57091 |
rs538292704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443480 | TCTCCAAAAAAAAAA[A/G]GAAGCTTGGATTTCA | 57091 |
rs538357856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56436946 | CGACCTCGTCTCAGG[A/G]TACAGGTAAGTCTGC | 57091 |
rs538454778 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443613 | TCACAGAGCAGAGGA[A/T]CCATGAGGCAGCTCA | 57091 |
rs538464022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424518 | GGTCAAGGCGGGTGG[A/C]TCATCTGAGGTCAGG | 57091 |
rs538487954 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413970 | ATTTTTATTGTTGTT[G/T]TTAAACTCTTTGAAA | 57091 |
rs538664639 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410522 | AGGCAGGTGAATGAC[A/G]AGGTCAGGAGATCAA | 57091 |
rs538698655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450263 | TCCCGACCTCAGGTG[A/G]TCCTCCTGCCTCAGC | 57091 |
rs538764821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444303 | CCCTCAGCTCTGCAT[A/G]TTGAAACCCTAACAT | 57091 |
rs538933563 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56423796 | GTGATCCGCACACCT[C/T]GGCGTCCCAAAGTGT | 57091 |
rs538947499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56448540 | ATGGGAACACTTGAT[G/T]GTTTGCTTTTGGGGA | 57091 |
rs539058147 | snp | C/G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454328 | GTCAAGGAGATAATT[C/G/T]GCTACTTTCAGCCCC | 57091 |
rs539230587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444800 | TTGAGCAATAACTGG[C/T]CAGGTGCTCTCAATA | 57091 |
rs539304214 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CASS4 | GRCh38.p7 | 20:56416529 | ATTCTGTTTACTTCC[A/G]TGTGTGTGTGTGTGT | 57091 |
rs539338333 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415342 | TAGGCCACCCCCACC[A/C]ACCCACGCAGTACCA | 57091 |
rs539356043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56431579 | CAAAATAAATCATAT[A/G]TCAAGAATAAGACTG | 57091 |
rs539383966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56432290 | TTGTTTTTTACTGAA[C/T]GGCAATTATTTGTCT | 57091 |
rs539405536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424728 | CCTGGATGACAGAGC[A/G]AGACTCTGTCTCAAA | 57091 |
rs539446230 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56437914 | CACAGGATGAAGGAT[C/T]ACCAGGACTGCCAGT | 57091 |
rs539480249 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444220 | AGTGCTGCATCCCGG[G/T]GACACCATGATGAAT | 57091 |
rs539492633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433074 | TCTGTCCTGGATCAT[A/G]GGACGCAGTCCAGAA | 57091 |
rs539885254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56440298 | TCGGAGCAGAGCTTT[C/G]CTGAGGTTTCTTCTA | 57091 |
rs539926179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433448 | AAAATCACACAGGGC[C/T]TTGATGGTTTGGGCA | 57091 |
rs539954701 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409893 | CTTTCATTCAGAAAA[A/G]CCATAGAGGGCTCAA | 57091 |
rs540025111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416055 | TAGAAATTTAGTTTT[C/T]GTGGGTTTTTTTGAG | 57091 |
rs540028394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451304 | CCTCAGGGGCGTGCT[A/G]TGATACAGTACACTT | 57091 |
rs540034087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56412606 | GTTGAATACCAGTGA[C/T]GTGTGAGTTGGAGAT | 57091 |
rs540211318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56431166 | TCAGTTCTCTCATCT[A/G]TAAAATGGGGATAAG | 57091 |
rs540268192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56431836 | TTTTTAAAGATTGCT[G/T]TAAATGTATTTCATG | 57091 |
rs540299235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56455372 | AATAACTGAGCTTGG[C/G]AAACTTACCTAGGTT | 57091 |
rs540330817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56425090 | GGAACATGTCCCATC[A/C]TGGGAGGCCCTCCTC | 57091 |
rs540348702 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56449897 | CTGAGAAAAAGAAAG[A/G]AGACATATTAGGTCT | 57091 |
rs540380366 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410745 | TCCGTCTCAAAAAAA[A/T]TAAATAAATAAAGGT | 57091 |
rs540558188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56430278 | GTTTGTTTCCCTATC[C/G]TCCTCCTGTTCTTCC | 57091 |
rs540599217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438414 | ATGGCATAGAAAACT[C/T]AAAGAGGCCTAAATG | 57091 |
rs540611118 | snp | A/G/T | 0.049324 | 0.150415 | intron-variant | CASS4 | GRCh38.p7 | 20:56432902 | AGTGTGGGCAGGGGC[A/G/T]TCACAGAAATCTTCC | 57091 |
rs540620756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56412822 | TAATTCCTTCTTTCT[C/G]TGGACCCCAAAGACA | 57091 |
rs540673944 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56454222 | AGACAGAAAGAAATA[A/C]TTTTCTGGATGAGTT | 57091 |
rs540791104 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56425766 | TTTAGGAATTCCAAC[G/T]GTACAAATGAACATG | 57091 |
rs540822438 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CASS4 | GRCh38.p7 | 20:56450363 | AGTCCATTGTTGAAT[A/G]TATACCCTGTTATGG | 57091 |
rs540827841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456473 | CCGCCTCACAGGTTC[A/G]GGCGATTCTCCTGCC | 57091 |
rs540877556 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454344 | GCTACTTTCAGCCCC[A/G]ACCTTTGTGTTCTGC | 57091 |
rs540891245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56457073 | TGACAAAGACAATCA[C/T]TGTTTTCATTTTCCA | 57091 |
rs540935470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444985 | CATGGAGGCATGTGC[C/T]TGTAGTCCCAGCTAC | 57091 |
rs540952642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451461 | CTGGCATTTCGCCGT[C/G]TCAGGGGGATGCATA | 57091 |
rs541154407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414345 | TGACCTTTTTTCTAA[A/G]CAGCCTAGATTTTTT | 57091 |
rs541242337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56440657 | ATCAACTGCTAGACT[A/G]ACATCCGTGTGAAAG | 57091 |
rs541383047 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CASS4 | GRCh38.p7 | 20:56419599 | GCCCGGCTAATTTTT[A/G]TATTTTTAGTAGAGG | 57091 |
rs541462250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413604 | CTTGAGCCTGGGAGG[C/T]AGAGGTTGCAGTGAG | 57091 |
rs541534141 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56445116 | GATCCATCTCAAAAA[A/C]AAAAAAGGTTTATAT | 57091 |
rs541649479 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424312 | TACCTGCAAATTCTT[A/C]AAGCAAGTTCTGGTT | 57091 |
rs541663706 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440090 | TACATTTTCTAACTC[C/G]CTGGGCTACAAGACA | 57091 |
rs541686469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433562 | TGAAAAACTCGAGGA[C/T]GACAACAGTGCCATA | 57091 |
rs541769184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456445 | GTGGCGTGATCTCAG[C/G]TCATTGCAATCTCCG | 57091 |
rs541779429 | snp | A/C | 5.16151e-05 | 0.00507985 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437471 | GCCCCGTTTATGAGC[A/C]GATGAGGAGTTGGGC | 57091 |
rs541800764 | snp | A/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411712 | CACGATAAGTTTATT[A/T]GATTTAAGAGAGAGA | 57091 |
rs541945433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445657 | CCTGCTTCAGGTGAA[A/C]TTCCCAGGTGAGGCA | 57091 |
rs541975098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420132 | TTGAGGCCACCTACC[G/T]GGCCACTCAGAGAGT | 57091 |
rs541990630 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56431640 | CCAGTGGGGTGGATG[A/G]TCATAAAAACCCCAT | 57091 |
rs542191049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56426314 | CATAAGGTTTTTGAA[C/T]ATCAAATGCGGTCAT | 57091 |
rs542236804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56419425 | GGAAAGCATCCCCAG[C/T]TCTCAGTGTGGGAGA | 57091 |
rs542367405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413480 | GAGTTTGAGACCAGC[C/T]TGATCAACATGAAAA | 57091 |
rs542383332 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56451140 | ATTGCACTTGTGTTC[A/G]GGAATAGGACTAATT | 57091 |
rs542435596 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56418349 | AAGAAGAGTAAACCA[-/AG]AGAGAGAGGGGTCAG | 57091 |
rs542437906 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421823 | GCCTTTCCTCACTTT[A/T]TTCCTTAAAAAAAGA | 57091 |
rs542442135 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56439163 | ATCTGTAACTTTTTA[A/T]AATATCAATTATTTT | 57091 |
rs542488799 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434604 | CCACTCCCAGCTAAT[-/T]TTTTTTTTTTTTTTG | 57091 |
rs542501471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56432892 | GTCATCCAAAAGTGT[A/G]GGCAGGGGCGTCACA | 57091 |
rs542549139 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CASS4 | GRCh38.p7 | 20:56440862 | GTTCTTGAGGTGGCC[A/T]CAGTAAAACCCCCCA | 57091 |
rs542591440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447201 | TGACAGAGCAAGACT[A/C]TGTCTGAAAAAAAAA | 57091 |
rs542842183 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425509 | AGTAGTTGACGATGT[C/T]TGGCATCCTGGAAGT | 57091 |
rs542879432 | snp | G/T | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56446701 | AGTAGCTCCCAACTT[G/T]CGTTGTATGCAAAAG | 57091 |
rs542943850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56453984 | TCAGGAGTTTGAGAC[C/T]AGCCTGGCCAACATG | 57091 |
rs542997758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56448320 | TAAATAGTATTTACT[A/G]TGATGATTGAGTTTT | 57091 |
rs543011380 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56440117 | GACATAGAACCAGAC[A/T]GTTGTTACATAGAAC | 57091 |
rs543049683 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56449194 | ATTCACAATAGCAAA[C/G]ACTTGGAACCAACCC | 57091 |
rs543145017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56418992 | ATTTTATTTCCTATA[A/G]AGCACACTTGGGGGG | 57091 |
rs543346115 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446134 | CAGAATACACATCAC[A/C]ACTCAGAGGCCAACT | 57091 |
rs543423808 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459714 | ACCTCAGGCCATCCC[C/T]CGCCTCGGCCTCCCA | 57091 |
rs543496780 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56451036 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAATGTT | 57091 |
rs543527056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56453883 | AATCTCTAAAAAAAA[C/G]AAAAGAAAAAAAAGA | 57091 |
rs543637046 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56434696 | ATCATCTGCCCCCTC[A/G]GCCTACCAAAGTGCT | 57091 |
rs543646591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56412916 | CCCTTGCCTGCAGCC[A/T]CCCGTGCTGAGCCCA | 57091 |
rs543675510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451767 | TAAACAACGCACTCG[C/T]GCCCTCTTTGGAAAG | 57091 |
rs543796905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414555 | AGTACAGGATTACAG[A/G]TGCACACCACCGAGC | 57091 |
rs543844152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56429692 | TCTTCCTCTGCCTGA[A/G]TGCTCTTTATCTGAC | 57091 |
rs543881999 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56415309 | CTTGTGTAGCAGCCT[A/G]TGTCATCTCAGTTTA | 57091 |
rs543905279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447490 | GGGACAAAGGTCCTG[C/T]TCACCTGGTTCTGTT | 57091 |
rs543995916 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427583 | CATTCTGCACTCTCT[C/T]GATGTTGAGTCTGGG | 57091 |
rs544060724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420192 | TTGTTCTTTTCCTTT[C/G]AACAACTGCTTCACC | 57091 |
rs544141707 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415711 | TTCATTCAGGGCCAC[C/T]GCAGATAGCCTTTCA | 57091 |
rs544145688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420771 | ATCAATAACAAACAA[C/G]TCAAGGTGCTCCTTC | 57091 |
rs544199237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56444360 | TACTGAGCAACAGCT[C/T]CTTGGGACGCCAGTG | 57091 |
rs544258185 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56437717 | GATTGCTGGCAATCA[C/T]GCTCGGGGAGCTTGT | 57091 |
rs544414602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442426 | CCTTATTCCTTGATC[C/T]TCTTTCACCTGACTC | 57091 |
rs544454103 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56435758 | TTTCTTTTTTCTTTT[G/T]TTTTGTTTTTGAGAC | 57091 |
rs544475179 | snp | G/T | 0.0577344 | 0.159793 | intron-variant | CASS4 | GRCh38.p7 | 20:56443100 | TGTGTTTCTGGGAGG[G/T]ACCACTGGCGGTACA | 57091 |
rs544486156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56455265 | TGTAAGTAAAAACAA[C/T]GGGTCCATTTAAAGG | 57091 |
rs544486570 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56426869 | CAGGCATGAGCCACC[A/G]CACCCAGCCAGCTTC | 57091 |
rs544492482 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56440815 | GAAACCGCAAGGAAA[-/T]TCAGGGGGGGTCCCT | 57091 |
rs544515520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56429184 | GCTCCTGCCTAGAGC[A/T]GCCATGCCTGCGGAT | 57091 |
rs544520954 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409810 | TGCAATGTTTGTCCA[C/T]ATTAAAGGCTCATTT | 57091 |
rs544540820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443883 | TCAGATCCCCCAGGC[A/G]AGAGTGGGATGCTTC | 57091 |
rs544553572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56449764 | ATGAGTCTCTCATAC[C/G]CTGTTTTTATTGCTG | 57091 |
rs544658034 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56435588 | AATAAGAAGGGGGCT[C/T]GGCCATCACTGCCGT | 57091 |
rs544706504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56429631 | ACACACTCACTCATA[A/C]TCACACACGCCCCCT | 57091 |
rs544728682 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56429672 | CTCCGGCCTCCACAC[A/G]TTCCTCTTCCTCTGC | 57091 |
rs544993125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442324 | CTTCATTTTACAGAT[A/G]AGGACATTAATTCCC | 57091 |
rs544994096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56449450 | AACATCACACACCGG[A/G]GCCTGTCATGGGGTA | 57091 |
rs545053231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443732 | GCACAACACGGCAGC[A/G]TGCAGGCTGGACGAG | 57091 |
rs545055408 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56426579 | TTCTTCTTTCCGCCT[-/C]CCCCCTCCCCCGCCA | 57091 |
rs545158529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56422347 | GACCTTTATTGTTGC[A/G]TCATTTCAATCCTGA | 57091 |
rs545196231 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450804 | TTTGAGAGGCCGAGG[G/T]GAGTGCATCACCTGA | 57091 |
rs545279742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56448028 | GTGCCTGTAGTCCCA[A/G]CTACTCGGGAGGCTG | 57091 |
rs545305223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56434800 | AATTGTGTGTTTCAT[A/G]TTATGCCATTAGATT | 57091 |
rs545322831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56449029 | CTGTAAACTAGTTCA[A/C]CCATTGTGGAAGACA | 57091 |
rs545325828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56415943 | AAACACGTGATATTA[A/G]TGATAGGAAACACTG | 57091 |
rs545338685 | snp | C/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409978 | ATGTAGGAGCTAGTT[C/G]ATATAATTTCAGGGC | 57091 |
rs545377179 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56443384 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 57091 |
rs545402902 | in-del | -/AAAC | 0.00398564 | 0.0444627 | intron-variant | CASS4 | GRCh38.p7 | 20:56420047 | AAAACTCCATCTCAA[-/AAAC]AAACAAACAAAAGAA | 57091 |
rs545441854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56422131 | TTGACTTGATCCAAC[A/G]GTTCCCCAAACCAAA | 57091 |
rs545478618 | in-del | -/TCT | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56426531 | AAGAGGATTTTTCCC[-/TCT]TCTTCTTCTTCTTCT | 57091 |
rs545542391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56415462 | TAAGATACATGTTTT[A/C]AGGTTTTACACAAAT | 57091 |
rs545764830 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56449472 | CATGGGGTAGGGGGA[A/G]TAGGGGGAGGGATAG | 57091 |
rs545775151 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56417385 | GCCTTGGATTCTTCT[C/G]TCTCTAGCAAGCATC | 57091 |
rs545857146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456397 | TTTTTTTTTTGAGAC[A/G]AAGTCTTGCTCTGTC | 57091 |
rs545912005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56418752 | ATCAAGGAGTAGATA[G/T]CTTCTATTTATGTGT | 57091 |
rs545954619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450805 | TTGAGAGGCCGAGGT[A/G]AGTGCATCACCTGAG | 57091 |
rs545973964 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432150 | GTATAGGCAATTTAA[C/T]TAAGGCATATTAGAG | 57091 |
rs546010864 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433887 | TTTCTATGGAAAAAT[A/G]AGTTAAAAGTGGGTA | 57091 |
rs546138371 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438470 | ATATCTTGGCATATC[A/G/T]CCACAACAAGCTGCT | 57091 |
rs546159129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56432768 | CTCAGCACCCACATT[C/G]TTGTGAAACCCACTC | 57091 |
rs546237115 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409568 | CATGCAAAAGCAATT[C/T]TCCTCCCTACGCATG | 57091 |
rs546365362 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458854 | CATACACCAATGAGC[G/T]GAAACAGACCTGGTG | 57091 |
rs546415428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445065 | CAGTGAGCCGAGATC[A/G]CGCCATTGCACTCCA | 57091 |
rs546537097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416089 | GAGTTTCACTCTGTC[A/G]TCCAGGCTGGAGTGC | 57091 |
rs546581697 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56448517 | AACTCAAGTCATTGA[A/G]TGGTCCCATGGGAAC | 57091 |
rs546598799 | snp | A/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409883 | TTTCTCACACCTTTC[A/T]TTCAGAAAAACCATA | 57091 |
rs546666404 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56455885 | GCGGTGAGCTGAGAT[C/T]GCACCACTGCACTCC | 57091 |
rs546675447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56423758 | CCATGTTGGCCAGGC[C/T]GGTCTTGAACTCCTG | 57091 |
rs546684268 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56423291 | TCTTCTGACATCCAT[G/T]TCCTACAACTCTTTG | 57091 |
rs546704542 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447791 | GGTCCATGACAAACA[C/T]ACAAGCTCCCTTTGC | 57091 |
rs546712283 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56417031 | TCAAGGTAAAAATGT[A/G]GAATTTTTTAAAAAA | 57091 |
rs546793038 | snp | A/C/T | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56429283 | GCCCATTCAGCAGTG[A/C/T]GTCCCTCCCTTCTCT | 57091 |
rs546904897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56430669 | CTGCTATTGCAATGT[C/G]CAGTGCTCCCTGCAC | 57091 |
rs546954257 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56454321 | GGGCTGTGTCAAGGA[A/G]ATAATTTGCTACTTT | 57091 |
rs547236390 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56429874 | TCATAACTTCCTGTA[-/T]TTTTTATAACTTCCT | 57091 |
rs547342727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444700 | ATTGAGCCAACATCA[C/T]TGAGCTCTGGAGGAT | 57091 |
rs547469710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56432179 | AGTGTGATTGCAAGG[C/G]TAAGTATGAAACTGG | 57091 |
rs547532626 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56425461 | CCTCCATGCTGTACA[C/T]GGTCCAGGCCCTTTG | 57091 |
rs547579349 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438686 | ACATAGTGAAACTCC[A/G]TCTCTATTAAAATAC | 57091 |
rs547642499 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450087 | CCCAGGCTGGAGCAC[A/G]ATGGTGCGATCTTGG | 57091 |
rs547676499 | in-del | -/ATC | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420453 | GAGTGCAGTGGCGTT[-/ATC]ATAGTTCACTACAAC | 57091 |
rs547700319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445299 | CCTCCCACTGCTGCC[A/G]GCAAAAGCTGCCAGC | 57091 |
rs547814076 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56451929 | TCCAGTGTCTCCAGG[A/G]AAGGCCAGCGTCAGA | 57091 |
rs547878791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446302 | TGCTTTGTTGACCAG[C/G]CTGGTCTCGAACTCC | 57091 |
rs547975265 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56417765 | CAGGTGTTTGGCAAC[A/G]GAGGTCATTCCTGAC | 57091 |
rs547989488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56425942 | CTCTTTTTAAAAAAT[G/T]TAATACTACATTTTG | 57091 |
rs548047308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56457334 | CATGTGCTAATGGAA[G/T]AGCCGGAGGCAGCCT | 57091 |
rs548088090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56455748 | CAGCCTGACCAACAT[G/T]GTGAAACCCCGTTTC | 57091 |
rs548276094 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455462 | GTACCTTCTCAGAGG[A/C]AAACTAGGACAAGAA | 57091 |
rs548336849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56425196 | TAGCAGGAAGGGCAG[C/T]GAGCCTCCCCCAGGA | 57091 |
rs548340171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438624 | AGCACTTTGGGAGGC[A/G]GAGGCGGGCAGATCA | 57091 |
rs548474063 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56418345 | GTCAAAGAAGAGTAA[A/T]CCAAGAGAGAGAGGG | 57091 |
rs548496717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424530 | TGGATCATCTGAGGT[C/T]AGGAGTTCGAGACCA | 57091 |
rs548520856 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411036 | ATCCTGGTGCCCAGA[C/T]TTGTGGGGACGACAC | 57091 |
rs548605578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56457184 | AGGAGACATAACCCC[C/T]TTCTGAAAAAATCAG | 57091 |
rs548648773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56458167 | TTATATATTACAGTG[C/T]TTTGAAAACATTAAT | 57091 |
rs548753038 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444301 | CTCCCTCAGCTCTGC[A/C/G]TATTGAAACCCTAAC | 57091 |
rs548756880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56439568 | ATAGTCCCAGCTACT[C/T]AGGAGGCTGTGGAAG | 57091 |
rs548762482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56432075 | TCAAAGATCGTTGAG[A/G]ATACTTGTCCAACTT | 57091 |
rs548765392 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56427474 | CTGCATTAATCTTTC[C/G]TAGCCTGTATTTGAA | 57091 |
rs548824381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56425328 | CAGTTAGATCCCATT[A/T]AACAGTCATTCGTTG | 57091 |
rs548938821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56426576 | CTTCTTCTTCTTTCC[A/G]CCTCCCCCTCCCCCG | 57091 |
rs548999961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56419751 | CTGCACTCTTAAAAC[G/T]CCTCTAGGAGGCCAG | 57091 |
rs549019062 | snp | G/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410312 | ATACAGCAGAAACAG[G/T]GGTTTCCAGGGGCTG | 57091 |
rs549096188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442030 | CATTCCAAATGGAAG[C/T]GGCTGTTGGTAGACG | 57091 |
rs549101036 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56413157 | GCCTGGGCAACATAG[C/T]GAGACCCCATCTTAA | 57091 |
rs549234284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56453241 | CTTTGGGGAGACACT[A/G]GTTCCATTTTCTAGA | 57091 |
rs549298408 | snp | A/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409706 | CCTCACTAGAGTCCT[A/T]CTGACGTAGTTCCCT | 57091 |
rs549437087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447574 | GGGGTATTCCTGTAA[A/G]TGCCCCCCACCTCCT | 57091 |
rs549451725 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CASS4 | GRCh38.p7 | 20:56434995 | AATGAACTTTTATTA[C/T]TTTTGTAGAAAGAAC | 57091 |
rs549512827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56435979 | CTGGTCTTGAACTCC[C/T]GGCCTCAAGTGATCT | 57091 |
rs549512914 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56428781 | ATTGGCAATAGCAGG[A/C]TTCAGTCAGATGGAT | 57091 |
rs549571493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445483 | CTCAGCCTAGCTAGA[C/T]GAATGTAGACGAATA | 57091 |
rs549586837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413867 | TCAGTAAATCCCTGC[A/G]TATCCTTCACCTAGA | 57091 |
rs549597488 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435230 | AATTCCATTTTTGTA[A/G]CAGAATAGAGATATT | 57091 |
rs549615775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446971 | CCAGCATTTTGGGAG[G/T]CCAAGGCAGGAGGAT | 57091 |
rs549667307 | in-del | -/AATA | 0.00517822 | 0.0506191 | intron-variant | CASS4 | GRCh38.p7 | 20:56449650 | TACACAGATAAAAAT[-/AATA]AATAAATAAATAAAT | 57091 |
rs549696066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56439511 | CCTCATCTTTACTAA[C/T]AATAATAAAAAATAA | 57091 |
rs549776805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56438835 | GCTCCCCAGCCTGGA[C/T]GCCAAGAGTGAAACT | 57091 |
rs549906586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56419054 | CCAAAACTTAAAAGG[A/T]CTGAGAATAGACAGG | 57091 |
rs550010453 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56458151 | TATAATATTGTATAT[A/G]TTATATATTACAGTG | 57091 |
rs550028719 | snp | C/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410067 | ACAACTTGTGAATTA[C/T]AGCATTCTGATCTGT | 57091 |
rs550131371 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56417496 | ATCTTACCTTCACTT[A/G]TTAAGATCTGAAATT | 57091 |
rs550151862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421770 | CGGCATAATTGCTTA[C/T]GACCCATCAAATAAC | 57091 |
rs550153558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414889 | TATATAAATAGTAGC[C/T]AACCCTTACCGATTG | 57091 |
rs550251334 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452735 | GAATTCGGGACCAGA[C/T]GCAGACCATCTCCAA | 57091 |
rs550273231 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56441260 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 57091 |
rs550389623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56419721 | CAGGCGTGAGCCACC[A/G]TGCCCGGCTAGGCTC | 57091 |
rs550465029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421105 | TCTCTGTCATGCATT[A/G]AACAGCTTGAGCCAG | 57091 |
rs550513062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413832 | AACCATTGGAAAAAT[A/G]TGGGAAGCGTGGGGG | 57091 |
rs550543712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446328 | ACTCCTGGCCTCAAG[C/T]AATCCTCCCATCTCA | 57091 |
rs550553860 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459435 | GCAATTCCTTATAGG[C/G]CTAGCTTGGTTCTTC | 57091 |
rs550573220 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56437762 | TGGAGAACTCAGCGG[C/T]CTCCACCCCCTTGTC | 57091 |
rs550747819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56427894 | CCGAAATGCGAAACA[G/T]GGACATTTTTCAAAG | 57091 |
rs550762683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56422859 | AAAGTTTTTCTTTTT[C/T]TCTCATATCCCTCCT | 57091 |
rs550938807 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56449375 | CAGAAAACCAAACAA[C/T]GCATGTTCTCACTCA | 57091 |
rs550996334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421058 | TAGAAAGATGGAAAA[C/G]TTTGGTGAACAAGCC | 57091 |
rs551013633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56430595 | AACTGCTTCCATCTG[C/T]TATTCACAAAGAGCT | 57091 |
rs551061127 | snp | C/T | 3.30278e-05 | 0.0040636 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453019 | AAATACATCCAGCCT[C/T]CCCAAAGAGAAACTG | 57091 |
rs551075903 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436507 | AACCCCATGAGGTAG[G/T]TATTACTATTATTAC | 57091 |
rs551104887 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428613 | GTCTCACTCATGTAT[A/G]TTTCTTGCCCAGCTC | 57091 |
rs551165228 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56449130 | ACCCAAAGGATTATA[A/G]ATCATGCTGCTATAA | 57091 |
rs551174709 | snp | A/G | 0.00398564 | 0.0444627 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459406 | ACAGCATAAATATGT[A/G]TGCCCTCTCATGTGC | 57091 |
rs551217579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56426645 | CAGTGGCACAATCCC[A/G]GCTCATTGCAATCTC | 57091 |
rs551277986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56441092 | CTCCTGGGTTCAAGA[C/G]ATTCTCCTGCCTCAG | 57091 |
rs551279106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56427709 | TCACATTTCCCATGT[A/G]TCAAAAGATCTGTGA | 57091 |
rs551339550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56434171 | TTGCTGGAGGGCAAC[A/G]TGACAGCATCCGGAG | 57091 |
rs551364181 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455855 | AGAATTGCTTGAACC[C/T]GGAAAGCAGAGGTTG | 57091 |
rs551478118 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56436044 | GGCGTGAAACACTGC[A/G]CCCAGCCTCTTGTCA | 57091 |
rs551548074 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56433386 | GGTGACACCCTGGAG[G/T]CCAGTGAGGAAGTGA | 57091 |
rs551567675 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56447639 | CAAGTCCCTCCAGGT[A/G]GACAAATGCATCTCC | 57091 |
rs551624774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56448381 | AACTGCTTTGCTCTC[C/T]TCCCCCTGGTCCTGA | 57091 |
rs551807566 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56436748 | AAAATTTAGCCCGGG[A/G]TGGCGGCACGCATGT | 57091 |
rs551816176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56442625 | GAGCTTTGTTTTACT[C/T]TTTATCCCAACTTCC | 57091 |
rs551855274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56429432 | CCCAGCTGGACCAGA[C/T]AATTGACTTTGAATC | 57091 |
rs552118272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416210 | ATGTGCCACCATGCT[C/T]AGCTAATTTCTGTAT | 57091 |
rs552146429 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417320 | CATTAGATCCCACTC[C/T]GAGCAGCTCTCCTGC | 57091 |
rs552173502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56454967 | ATTACTGAAATGACT[A/G]TAGGGGCTCTGCAAG | 57091 |
rs552185810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56418272 | GAACAGCAGATGCCA[A/C]GGGCCTGCAGTGGGA | 57091 |
rs552209667 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56450010 | CTCTCTTGTTTGCCC[C/G]CCAACCTTTGGTTGA | 57091 |
rs552209925 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409641 | CAGAAAAGAAAATTC[A/G]GTCCAAACTACTGTT | 57091 |
rs552273054 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CASS4 | GRCh38.p7 | 20:56444126 | GGTGGATTTTTACAC[C/T]GTGTGCTAATGTTTA | 57091 |
rs552318407 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411226 | GAGCCTGGCTTGGAA[A/G]AATGGGCACCATTTT | 57091 |
rs552335690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444522 | AGACAGCATCTTCTA[C/T]TCTAGAAAAATGTGC | 57091 |
rs552372378 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433068 | CCCTACTCTGTCCTG[A/G]ATCATGGGACGCAGT | 57091 |
rs552490739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56430791 | GGAGGAGGATCTGGC[A/G]GAAGAGAGTTCTGGG | 57091 |
rs552536667 | in-del | -/G | 0.000635728 | 0.0178174 | intron-variant | CASS4 | GRCh38.p7 | 20:56453230 | TAGTGTATAGGCTTT[-/G]GGGAGACACTGGTTC | 57091 |
rs552550644 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56449246 | TGGATTAAGAAAATG[G/T]GGCACATATACACCA | 57091 |
rs552679572 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CASS4 | GRCh38.p7 | 20:56436334 | AATGGATTGCTATAT[A/G]TATGTGTGTGTGTGT | 57091 |
rs552679737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56428966 | TTTCTGCAGCTTTGC[C/T]CTTTTGAGTAAACTA | 57091 |
rs552700431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442294 | ATCTCTGCATATCTT[C/T]AGATTAGAACAACTC | 57091 |
rs552726544 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56453595 | CAGCTACTCTTAGAA[A/C]TACTTTTCTGAGGCT | 57091 |
rs552786282 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56444602 | GGAGACTTGGCAGCT[A/G]TATTATTTTAAAGTT | 57091 |
rs552794132 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56431281 | ATTCCCTGTTTTCCC[G/T]CCATTCCAGGTAAGG | 57091 |
rs552829957 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56428595 | ATGTCTTACGCCTGG[C/T]CTGTCTCACTCATGT | 57091 |
rs552929704 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421277 | CAAACCTGTAATTTC[A/T]TGGGTAACATCGCTG | 57091 |
rs552963997 | snp | A/T | 0.0456336 | 0.143994 | intron-variant | CASS4 | GRCh38.p7 | 20:56455134 | TGTTCTTCCTTTTTT[A/T]AAAAAAAAAAAGTCA | 57091 |
rs553000066 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CASS4 | GRCh38.p7 | 20:56442775 | GTGAAACTGCTTTTG[A/G]ATCCACTAGTTCCTG | 57091 |
rs553141668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56429604 | CTTTCCATGCGCCCC[C/G]AACACATACATACAC | 57091 |
rs553212493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447244 | AAAAATTAAAAAAAA[A/G]AGAAGTCACTTTAGC | 57091 |
rs553233910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56443617 | AGAGCAGAGGAACCA[C/T]GAGGCAGCTCACAAA | 57091 |
rs553279678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56453662 | GGGAGGCCAACGCAG[A/G]AGGATCCCTTGAGGC | 57091 |
rs553329363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416432 | TAAGTTCTTATTTTG[G/T]ATTTTTGGTAGTTTC | 57091 |
rs553473642 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56437771 | CAGCGGCCTCCACCC[C/T]CTTGTCGTTGACACC | 57091 |
rs553517216 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415016 | CACAGACGAGGAAAC[A/G]AGGCCTCGCTGACTT | 57091 |
rs553638054 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450941 | TGGGAGGCTGAGGTG[A/G]GCAGATCACTTGAGG | 57091 |
rs553639255 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CASS4 | GRCh38.p7 | 20:56422937 | CTGGATAAACCGGCC[A/G]CAAAGGCTATTTGCA | 57091 |
rs553785073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424138 | TCCTTTATGTGAGAT[G/T]ATGCAAGAAACTACT | 57091 |
rs553839654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417900 | GCAAGCTGTTGCTAT[G/T]GAAATCAAGGTCACA | 57091 |
rs553880051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56425775 | TCCAACTGTACAAAT[A/G]AACATGGACTCAAAG | 57091 |
rs553941996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56439639 | TATTATTACTACGGC[A/G]CCCCTGCACTCCAGC | 57091 |
rs554055757 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56422049 | GAAACTGAAACCCAG[A/G]GAAGTTCTGTTACTT | 57091 |
rs554065924 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425335 | ATCCCATTTAACAGT[A/C]ATTCGTTGCCCTCTC | 57091 |
rs554103983 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412032 | GTTCGGTTGGAGTTG[C/T]TCCACAGAGTTCAAA | 57091 |
rs554138204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56430879 | AAGTAAGAAAACAAT[A/G]TGACTGGAGGGAAAT | 57091 |
rs554145566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56439002 | GGTTAAAGAGAAAGG[G/T]AGCAGTAAGCTGGGG | 57091 |
rs554152855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445043 | TGAATCCAGGAGGCG[G/T]AGTTTGCAGTGAGCC | 57091 |
rs554253891 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56449162 | GATACATGCACACGT[A/G]TGTTTATTGCGGCAC | 57091 |
rs554255276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56430190 | GATGAGCACATTGCA[C/T]CTGCCAGCTGTGGAA | 57091 |
rs554342963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56423040 | TGGCTGGGGTGGCAG[A/G]AAGGGCAGTGAGCCT | 57091 |
rs554366982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456337 | CTTAAGATGCTCATA[A/G]TCTGATGCCTACCTC | 57091 |
rs554430172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450772 | GGCACGGTGGCTGAA[A/G]CCTGTAATCCCAGCA | 57091 |
rs554607064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438315 | AAAGTATATCCCCTT[C/G]AATGCAGAAATTTTA | 57091 |
rs554670730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56431819 | ACATTTCAGATGATC[A/G]GTTTTTAAAGATTGC | 57091 |
rs554719421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417233 | AGGTGGTGAGCAAGA[C/T]ATTTCAAACTCAGTC | 57091 |
rs554730842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445516 | TCAGTATCAGAGTCA[C/T]AGCCTCCTGGTCCCT | 57091 |
rs554752564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56449357 | CACAAACTATTGCAA[A/G]GACAGAAAACCAAAC | 57091 |
rs554792658 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409692 | GAGCATTAAGATTAC[C/T]TCACTAGAGTCCTTC | 57091 |
rs554806136 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459040 | ATATTTTATATTGAT[A/T]AAATGTGTGCATGTT | 57091 |
rs554806953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443109 | GGGAGGTACCACTGG[C/T]GGTACAGCCAGTGGT | 57091 |
rs554807309 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410708 | TACACCACTGCACTC[A/C]AGCCTGGTGACAGAG | 57091 |
rs554868342 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CASS4 | GRCh38.p7 | 20:56443550 | CTAGACCAATCAGCC[C/T]GAGACCATCAGGAAC | 57091 |
rs554893431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56456966 | GCTGGGATTACAGGT[A/G]TGGGTCACTGCACTC | 57091 |
rs554945433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450320 | TGAGCCACCACGCCC[A/G]GCTGAGAAGTCTCTT | 57091 |
rs554950056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444920 | GTTCAAGACCAGCCC[A/G]ACCAATATGGTGAAA | 57091 |
rs554956707 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56457585 | TAGGTCAGGGTATTT[A/T]GTTGCTTCTGGAAAT | 57091 |
rs554977872 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456650 | AAAGTGCTGGGATTA[C/G]AGGTGTGAGTCACCG | 57091 |
rs555035471 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433417 | TACCTATGAGTCTGG[A/C]AGTGTGGGAAGAGGC | 57091 |
rs555068155 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56419125 | AATCAAAACAGGGCC[A/G]TTTTGGAATTGCGAT | 57091 |
rs555130926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56432524 | AGGCGTGCACCACCA[C/T]GCTGGACAATTTTTG | 57091 |
rs555160188 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417869 | TCCTTGTCCATGGTC[A/G]GATGTTGCCTTAGAT | 57091 |
rs555283510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456308 | TTTTCACCTCCCTAC[A/G]GTTAATATTTTCACT | 57091 |
rs555287088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450741 | TCCTCTCAGAAATGT[A/T]ATTAGCTTGGGGCCA | 57091 |
rs555386673 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56426088 | CTTTGCCATCTTGTA[A/T]CTGCTAAGATGTCCA | 57091 |
rs555416164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451729 | GGGAGCCACTGAAGG[A/G]GCGGCGGAGTGACGA | 57091 |
rs555438955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56412801 | CGAGTCTGCCTCAGC[A/C]CCCGCTAATTCCTTC | 57091 |
rs555482872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446054 | CTGCGCCCAGAGTCT[C/G]GGGTTCTTGGGATCA | 57091 |
rs555531337 | snp | A/C | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56428160 | CATGATCTCTACTTT[A/C]CTATCCCATAGTTAC | 57091 |
rs555590792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420630 | GAACTCCTGACCTCA[A/T]GCAGTCCTCCTGCCT | 57091 |
rs555646431 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56418678 | GTAGAACTTTTGATG[G/T]TTGAGACCGCTGGTC | 57091 |
rs555682402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446420 | ATATTTAATATATGT[A/G]TGTGTGTACATACAC | 57091 |
rs555722792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56427005 | GATCATCTTTGCTGT[A/G]ACTCCCTAAGCTAGG | 57091 |
rs555787803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56434514 | CCATTTCAGCTCACT[A/G]CAACCTCTGCCTCCC | 57091 |
rs555802536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420155 | CAGAGAGTTTCTCCA[C/T]GAGTTTATGTTAGTG | 57091 |
rs555919101 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56456434 | GTGGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAT | 57091 |
rs556002008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56439931 | TTGGCAAGGTCTGTG[C/T]GCAGGGAAAGGCCAA | 57091 |
rs556059620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56440544 | TGCTCATGCCACTCA[A/G]TACAATGACAGGCTC | 57091 |
rs556074394 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425553 | AAGTCTTCCTGCATG[G/T]GGCAAACTGCTTTTG | 57091 |
rs556094640 | snp | A/G | 0 | 0 | intron-variant | CASS4 | GRCh38.p7 | 20:56430954 | AGCCACACTAGGAAG[A/G]TGACCTTTTGTTCTG | 57091 |
rs556122835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433486 | GGCTTTGTCCAAAGG[G/T]TAATAGGGAGCCACT | 57091 |
rs556382607 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CASS4 | GRCh38.p7 | 20:56444078 | TTGCGGCTGCTTTGT[C/T]TGCATCCGTGAGTCT | 57091 |
rs556396493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56431589 | CATATATCAAGAATA[A/G]GACTGCTGCTATTCA | 57091 |
rs556417717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56426863 | GGATTACAGGCATGA[A/G]CCACCGCACCCAGCC | 57091 |
rs556439272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56457450 | GGATTTGGGAGAAGT[C/T]GGTTCCATTTTCCAG | 57091 |
rs556471742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56412619 | GACGTGTGAGTTGGA[A/G]ATGGGAAAGTTTAAC | 57091 |
rs556500552 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451684 | GAGGCTCAAAAGAAT[A/C]CTGAAGGACCTTGAG | 57091 |
rs556531441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56433079 | CCTGGATCATGGGAC[A/G]CAGTCCAGAACAAGA | 57091 |
rs556532458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424782 | CAGGTTCTTTCTTGG[C/G]TAACTATGTCAAAGG | 57091 |
rs556560886 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CASS4 | GRCh38.p7 | 20:56447165 | ATGAGCTGAGATCAC[A/C]CCACTGTACTCCAGC | 57091 |
rs556593143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56426212 | CGTTGGCCCTTGATC[A/G]CTGAACTACCTTAAG | 57091 |
rs556623191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56441448 | TGTCTCTACTAAAAA[A/C]ACAAAAATTAGCCAT | 57091 |
rs556676623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451377 | TCTATGTTTATAATT[A/G]GATTCTACCACATGT | 57091 |
rs556686403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442192 | CCCAAATTAACATCC[A/G]AGAAGGTGGAAACAT | 57091 |
rs556715249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420007 | GAAATCACGCCATTG[C/T]ACTCCAGCCTGGGCA | 57091 |
rs556802709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413401 | AGTGTGGCTGTCTGC[A/G]GTGGCTCACACCTGT | 57091 |
rs556892741 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459716 | CTCAGGCCATCCCCC[G/T]CCTCGGCCTCCCAAA | 57091 |
rs557015028 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452924 | CCATTGTCATTGCCA[A/G]TGGAAGGCTCCTTTT | 57091 |
rs557087716 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56439065 | CGTGGGACCAGGCCT[C/G]GCCTGGGGTAGGTGC | 57091 |
rs557124357 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441340 | CTGGGTGCGGTGGCT[C/G]ACACCTGTAATCCCA | 57091 |
rs557268932 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433844 | GCCCCTCACAATACA[C/T]ATGCCCCTAACTCCT | 57091 |
rs557305509 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56421002 | AAGCTTAAACAAAAG[A/C]GTGGCTCCTTGCTTT | 57091 |
rs557367621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56415314 | GTAGCAGCCTATGTC[A/G]TCTCAGTTTACGTAG | 57091 |
rs557381336 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415859 | TGCATGGCAGATTTT[A/G]TGTAATATCCAGACT | 57091 |
rs557414430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56446486 | ACCACAGTCTTAACA[C/T]GGATTATCACTGATT | 57091 |
rs557462162 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56413242 | ACCCAGACATAAAGA[A/G]AGTGAAGCTCAAGGT | 57091 |
rs557476059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447069 | AAAAATTAGCTGGGC[A/C]TGGTGGTTCACGCCT | 57091 |
rs557626587 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448900 | AATGCAAATCAAAAC[A/C]ACCATGAGCTACCAT | 57091 |
rs557672491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56429463 | GCCTCTCTGGCTTCC[A/G]CTTGCTCCATGCACC | 57091 |
rs557878548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56440663 | TGCTAGACTGACATC[C/T]GTGTGAAAGGAAAGA | 57091 |
rs558031005 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56457611 | GAAATGTTGAGAGTT[C/G]TGATATATCTCTGAT | 57091 |
rs558077509 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56441378 | GGGAGGCCAAGGCGG[G/T]TGGATCACCTGAGGT | 57091 |
rs558200514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414370 | TTTTTTATGATTTAG[A/G]CTTCTTTTTATGTAC | 57091 |
rs558313544 | snp | C/T | 0.000484047 | 0.0155496 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452417 | TCGTTTCCTCGTGCT[C/T]CACCACATCCACCGA | 57091 |
rs558339958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433626 | TGTGAAGGAACAATT[G/T]GCTGACCCAGAAAGA | 57091 |
rs558387427 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459774 | ATTCCTGGCATGTAC[A/G]TGTTTTAAATTCACT | 57091 |
rs558484946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56449541 | GGTGCAGCACACCAA[C/G]ATGGCAGATGTATAC | 57091 |
rs558521796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56428274 | TGATGCTGCCCTGAC[C/T]CCTGTGACAGGAAAG | 57091 |
rs558531052 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454053 | GGGCATGGTGGTGTG[C/G]GCCTGTAATTCCAGC | 57091 |
rs558592442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56436992 | TTTCACTTAGACCCC[A/G]AGGATGTGAAGGAAC | 57091 |
rs558608299 | snp | C/G/T | 0.00011613 | 0.00761925 | missense | CASS4 | GRCh38.p7 | 20:56450663 | CAGGACTCCATCCCC[C/G/T]AGACAGCCAAGCAAG | 57091 |
rs558651880 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56430095 | CAATACAATCTTGGT[A/G]AATGAATGAATGAAT | 57091 |
rs558705635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56422997 | GTGTGGGAGAGAATG[C/T]GTTATGTAACCAGCC | 57091 |
rs558741226 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56454383 | CTGGTGGTGTAGGAG[C/G/T]TTTAACATGTTCTAG | 57091 |
rs558747296 | in-del | -/CT | 0.0115144 | 0.0749975 | intron-variant | CASS4 | GRCh38.p7 | 20:56431271 | ATTCAGTATAATTCC[-/CT]GTTTTCCCTCCATTC | 57091 |
rs558791468 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CASS4 | GRCh38.p7 | 20:56416533 | TGTTTACTTCCGTGT[A/G]TGTGTGTGTGTGTGT | 57091 |
rs558793338 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56423797 | TGATCCGCACACCTC[A/G]GCGTCCCAAAGTGTT | 57091 |
rs558831850 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56437693 | TCAAACACGCAAAAC[C/G]GGAGCCCAGATTGCT | 57091 |
rs558868000 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56455931 | AACAAGACTCTGTCT[A/C]AAGAAAACAAACAAA | 57091 |
rs558873426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56448572 | TGAAAGGCAACCCCC[A/G]CTACACCGCACCCCA | 57091 |
rs558902620 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410558 | TCCTGGCCAACATGG[A/T]GAAACCCTGTCTCTA | 57091 |
rs558928326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56427557 | GAAAGATGATCAAAG[A/G]GCCCTTTCTCCATTC | 57091 |
rs558937897 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443072 | AAAGGGTCTGCGGGG[G/T]GAGAAAGCTTGGTGT | 57091 |
rs559005334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56456363 | ACCTCATTACTTCTC[A/G]TTATTTCTAAACTCT | 57091 |
rs559084927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56426602 | CCCCGCCAAGACAAG[A/G]TCTCACTCTGTCTTC | 57091 |
rs559128326 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56430093 | CTCAATACAATCTTG[A/G]TGAATGAATGAATGA | 57091 |
rs559228153 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56421007 | TAAACAAAAGAGTGG[C/T]TCCTTGCTTTCCTGA | 57091 |
rs559265600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56434107 | GATTAGGGTACAAGG[A/G]ACTGTGCAGTCTCAT | 57091 |
rs559300585 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56446702 | GTAGCTCCCAACTTT[C/T]GTTGTATGCAAAAGC | 57091 |
rs559401040 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413143 | GAAGTTTGAGTCCAG[C/T]CTGGGCAACATAGCG | 57091 |
rs559452906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446283 | TCTTGTTGAGATGGG[G/T]TCTTGCTTTGTTGAC | 57091 |
rs559475897 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433957 | TATTCCCTCAGCGGC[A/C]TGAGGGCTGCAGCTG | 57091 |
rs559492456 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459275 | CTGAACCCAGCCAAC[C/G]AATGCATTCATAACA | 57091 |
rs559542055 | snp | A/G | 1.66021e-05 | 0.0028811 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452542 | GTGGTCAGCTCTGTC[A/G]CTGGCCTGATGCTCT | 57091 |
rs559609789 | in-del | -/A | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411546 | GAAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 57091 |
rs559617541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56454009 | AACATGATGAAACCC[C/T]ATCTCTACTAAAAAT | 57091 |
rs559748537 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438148 | TAAAAATTAGCCAGC[A/C]TAGTAGCACACATGT | 57091 |
rs559781553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443254 | TGGGAGGCTGAGGCA[A/G]GTGGATCACTTGAGG | 57091 |
rs559788454 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409918 | GCTCAAATAACAGAC[A/C]GAGAGGTCAAGTTCC | 57091 |
rs559868353 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56436004 | TGATCTGCCCTCCTC[A/G]GCCCCCCAAAGTGCT | 57091 |
rs559932156 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56436610 | CTACCCCACTATGTG[C/T]GCTATGCTGCACTGA | 57091 |
rs559967721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56415454 | TGCATCTATAAGATA[A/C]ATGTTTTAAGGTTTT | 57091 |
rs560121575 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56431863 | CATGGGAATTACGAT[G/T]AAATATACCATAATT | 57091 |
rs560131658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424473 | CGGCCAGGCATGGTG[A/G]CTCACGCCTGTAATC | 57091 |
rs560182793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56425170 | AAAGGAGAGTTCAAG[A/G]ATCACTGGGATAGCA | 57091 |
rs560226302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56455450 | GGATAAGGTCATGTA[C/T]CTTCTCAGAGGCAAA | 57091 |
rs560231900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56416106 | CCAGGCTGGAGTGCA[A/G]TGGCATGATCTTGGC | 57091 |
rs560249291 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418579 | GTGGAGACTTCAGTG[C/T]AGGTGGCTTCATTTT | 57091 |
rs560284319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56449946 | GGCTTAATTTTAAGA[C/T]GAACTCAAGATAAAT | 57091 |
rs560285065 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56455672 | TGGTGGCTCACGCCT[C/G]TAATCCCAGCACTTT | 57091 |
rs560288555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456081 | GGTCCAAGGACCTCA[A/C]TTGGAAAGCCCCCGC | 57091 |
rs560394762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56429772 | TGGAAGCTTCCATGG[C/G]TGCTTTCTCAGGTAA | 57091 |
rs560399532 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416229 | TAATTTCTGTATTTT[C/T]AGTAGAGACGGGTTT | 57091 |
rs560438082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444001 | GTCACTCAACGAAGG[A/G]GGCTGTTTTGACATG | 57091 |
rs560442553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56423315 | CTCTTTGATTGTGTG[A/G]GACTCTGAGTTGACT | 57091 |
rs560457915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56430310 | TCCAAATGCATATTC[A/G]TTTTCCTTTTCCCTC | 57091 |
rs560574099 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443295 | AAAACCAGCCTGGCC[A/C]ACGTGGTACTAAAAA | 57091 |
rs560624348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416078 | TTTTTGAGGTGGAGT[C/T]TCACTCTGTCGTCCA | 57091 |
rs560629814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450413 | CCCTGCGTTGCCTCA[C/G]ACAAGGAAGGCGGGA | 57091 |
rs560660992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416607 | TAGCATCTTCATACA[C/T]AGCCCTTTTTTCCCC | 57091 |
rs560668526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438415 | TGGCATAGAAAACTC[A/C]AAGAGGCCTAAATGT | 57091 |
rs560809678 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56454779 | GCTTCTGATTCATAC[A/G]CTCTATTGCTAGATT | 57091 |
rs560819644 | in-del | -/GACA | 0.00119737 | 0.0244387 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411066 | ATGGGACAACCAGAG[-/GACA]GACAAGACGCTAAGT | 57091 |
rs560837211 | in-del | -/TGTGTA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436360 | GTGTGTGTGTGTGTG[-/TGTGTA]TATATATATATATGT | 57091 |
rs560877792 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56433001 | ACTTGAAAATGGGGG[C/T]GTTATGTCACGCCTC | 57091 |
rs560988783 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56429201 | CCATGCCTGCGGATG[G/T]CTCTTATACCACCAT | 57091 |
rs561011759 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56431104 | GGATGTGAGGAACCA[A/G]TTAGAATTTAAGTGA | 57091 |
rs561036822 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434415 | AAATGTTTATTGACA[C/T]GGAAAGATGCTCACA | 57091 |
rs561067013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56435875 | CCTGACTCAGTCTCC[C/T]GAGTAGCTGGGACTA | 57091 |
rs561076789 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | CASS4 | GRCh38.p7 | 20:56421791 | ATCAAATAACACAAA[A/T]CTCCTTCTTTCTTTA | 57091 |
rs561143617 | snp | C/G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409818 | TTGTCCACATTAAAG[C/G/T]CTCATTTGCCTTAAA | 57091 |
rs561262039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56429727 | ACTTTATCTGACTAA[C/T]TCCTTATCTAACTCC | 57091 |
rs561400296 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56422787 | TATTCACAGCATGTG[C/T]CATTCTCCACGATTA | 57091 |
rs561464034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444391 | GGAAGTACACTCCCC[C/G]TGTCCTGGACTCCGG | 57091 |
rs561608301 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445692 | AAGAACATCGTGGGC[A/C]ACGTGCGAGGAAGGC | 57091 |
rs561638204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456453 | ATCTCAGCTCATTGC[A/C]ATCTCCGCCTCACAG | 57091 |
rs561641423 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427280 | CTGTAGATACTTTGA[-/T]TTTTTCCTCAGGTTG | 57091 |
rs561677276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450938 | CTTTGGGAGGCTGAG[A/G]TGGGCAGATCACTTG | 57091 |
rs561740731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56445117 | ATCCATCTCAAAAAA[A/G]AAAAAGGTTTATATG | 57091 |
rs561747883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438629 | TTTGGGAGGCGGAGG[C/G]GGGCAGATCACAAGG | 57091 |
rs561817384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413057 | AGAAAGGTGAAAGAA[A/G]CCAGGCACGGTGGTA | 57091 |
rs561938368 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411145 | TAAAAATAAAAAATT[A/T]AAAAATGCTGTCTGA | 57091 |
rs561972306 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411724 | ATTTGATTTAAGAGA[C/G]AGAATACAGGTGCGG | 57091 |
rs562272275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56426323 | TTTGAATATCAAATG[C/T]GGTCATCAGTGCTGA | 57091 |
rs562410334 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411678 | TGCATGAGCTAGCAG[A/G]GGTTTCAAGTACAAC | 57091 |
rs562440608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450906 | GGGTGTGGTAGTGGG[C/T]GCCTGTAATCCCAGC | 57091 |
rs562450707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56418871 | TTCCAAGTCCAAGTG[C/T]CTGGTCCCCTTTCTC | 57091 |
rs562458745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456121 | ACAGCACTTCTCAGT[A/G]GAGGCCCGGGGCACC | 57091 |
rs562481097 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410900 | GTTCCCTCCCTGTTA[A/T]CTGCTATCGCCTGCA | 57091 |
rs562483996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56437886 | GCACTGAGGATGTTC[A/G]TGGCACCCTTTTCAC | 57091 |
rs562547046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444524 | ACAGCATCTTCTACT[C/G]TAGAAAAATGTGCGC | 57091 |
rs562556050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56418308 | TTCAGCATAGTACAG[A/G]GCCCCTGTAAAGACC | 57091 |
rs562632081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56455652 | CTCACATGGCTGGCC[A/G]GGCATGGTGGCTCAC | 57091 |
rs562678744 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410128 | TAGGGAAGAATCACT[A/G]CCGGGAGTCTGCCAA | 57091 |
rs562682550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56419325 | AGTGTTTGTTCAGGG[A/G]AAGAGCAGCCTTGTA | 57091 |
rs562687462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56423605 | GCTGGAATGCAGTGG[C/T]GCAATCTCAGCTCAC | 57091 |
rs562724541 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56424235 | GCTGTCTCAAGTTTA[A/T]CAACCTCATAAACTA | 57091 |
rs562724637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416940 | TTAAATTCAGCCTCA[A/G]TTAAAGAGCAAATCT | 57091 |
rs562833696 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56449376 | AGAAAACCAAACAAC[A/G]CATGTTCTCACTCAC | 57091 |
rs562993060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56457154 | TCCTTGTCTAACTTC[C/T]CCTCCAACCCTACTA | 57091 |
rs563031449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445078 | TCGCGCCATTGCACT[C/T]CAGCCTGGGCAACAG | 57091 |
rs563098891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438558 | AACAAAAACCAAACA[A/G]ATATAAACTCAAAAA | 57091 |
rs563201662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433897 | AAAATGAGTTAAAAG[C/T]GGGTACAGCAGGGAG | 57091 |
rs563219002 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446135 | AGAATACACATCACC[A/C]CTCAGAGGCCAACTT | 57091 |
rs563233670 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56436878 | GGCAACAGAGTGAGA[A/C/T]CCTGTCTCAAAACCA | 57091 |
rs563244302 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56425203 | AAGGGCAGCGAGCCT[C/T]CCCCAGGAGCTTTGA | 57091 |
rs563264038 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56427392 | TTGGAAACTTTTTTT[A/T]AACATAATATCCTTT | 57091 |
rs563296066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433299 | ATGTGTGGAATTTCA[A/C]TGGGTGGAAAGCTGC | 57091 |
rs563491352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56453196 | AGTAGTGGCTACTAA[A/G]ATGCTGAGACTCTTT | 57091 |
rs563497267 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428162 | TGATCTCTACTTTAC[C/T]ATCCCATAGTTACTA | 57091 |
rs563498831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56457228 | CTGTCTGAATGCTTC[C/T]GGGCTATGAATTTTG | 57091 |
rs563545624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447494 | CAAAGGTCCTGCTCA[A/C]CTGGTTCTGTTGGCA | 57091 |
rs563695325 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56445718 | AAGGCTGCCTCCACC[C/G]GGGAGCCTCCCACCC | 57091 |
rs563718398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56453893 | AAAAAGAAAAGAAAA[A/G]AAAGAGTTGGGATAT | 57091 |
rs563748121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56441993 | AGCCATTAACCCTGA[A/G]GCTAAACCCGCCCAG | 57091 |
rs563758574 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56446108 | ACCATGGCGGCCAGG[C/G]GCTCAGCCTCCAGAA | 57091 |
rs563779452 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CASS4 | GRCh38.p7 | 20:56448128 | GCCTGGGAGACAGAG[C/T]GAGACTCTGTCTCAA | 57091 |
rs563859715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420207 | GAACAACTGCTTCAC[C/T]TTATCATCAAGAGCA | 57091 |
rs563897271 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445773 | GAGCCTGCCAGCGGG[A/G]GTGCCGGGCGACCCC | 57091 |
rs563964747 | in-del | -/T | 0.41833 | 0.184838 | intron-variant | CASS4 | GRCh38.p7 | 20:56450031 | TTTGGTTGAGAGGTC[-/T]TTTTTTTTTTTTTCT | 57091 |
rs563971662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451056 | AAAGAAATGTTATTA[C/G]CTTGGTCAAAAATTA | 57091 |
rs564009193 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414658 | ATTCTGCTATTAATA[G/T]TATACAGATAGGCCG | 57091 |
rs564039213 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56451472 | CCGTGTCAGGGGGAT[A/G]CATAGGGGTTTGGTG | 57091 |
rs564184973 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56444992 | GCATGTGCCTGTAGT[-/C]CCAGCTACTCAGGAG | 57091 |
rs564195571 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant | CASS4 | GRCh38.p7 | 20:56412284 | CTTATCGTGCTTTCC[A/G]GAAAGTTTGCCTGCT | 57091 |
rs564277191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456519 | GCTGGGACTACAGGC[A/G]CCTGCCACCACACCC | 57091 |
rs564292215 | snp | C/G | 0.000131798 | 0.00811675 | missense | CASS4 | GRCh38.p7 | 20:56458477 | CAGCCTCAGCAGCAG[C/G]CAGCCCGCGGAGATC | 57091 |
rs564505566 | snp | C/T | 0.000543572 | 0.016477 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452724 | CCTTCAGAACAGAAT[C/T]CGGGACCAGATGCAG | 57091 |
rs564539254 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CASS4 | GRCh38.p7 | 20:56430057 | GATGCCTCCAGCAGA[A/G]CCCCTGGAATACACG | 57091 |
rs564547387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56429114 | CAGGAACAGGGACAA[G/T]GAGGCAGCATAACTG | 57091 |
rs564566023 | snp | A/G | 6.64165e-05 | 0.00576228 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453071 | CTTCCACTAAGCAAA[A/G]GGAAGATGAACACTC | 57091 |
rs564672096 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448466 | CCCAAGCCAGAGTCA[G/T]CGCCCAACCACTGTG | 57091 |
rs564724115 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56419613 | TGTATTTTTAGTAGA[A/G]GTGGGTTTTTTTTCA | 57091 |
rs564770555 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455865 | GAACCCGGAAAGCAG[A/G]GGTTGCGGTGAGCTG | 57091 |
rs564796538 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56417310 | CTTCAGGGCCCATTA[A/G]ATCCCACTCCGAGCA | 57091 |
rs564813676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420173 | GTTTATGTTAGTGAA[C/T]GTATTGTTCTTTTCC | 57091 |
rs564855965 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56422235 | GAATGAACACACTAC[A/G]ATCTCTGGAGCACTT | 57091 |
rs564871678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56415466 | ATACATGTTTTAAGG[C/T]TTTACACAAATAGGA | 57091 |
rs564882540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56428643 | CCTATAATCCTTTGA[A/G]TTTGCTGCTTCTCCT | 57091 |
rs564896405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443393 | AGAATCGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 57091 |
rs564962599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443813 | GACCCGGAAACCCCT[C/T]GTCTGAAGCGCTACA | 57091 |
rs565035104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56447358 | CAGCTTGGGCCTGCC[C/T]GCTGGGCTGGGCTCC | 57091 |
rs565054350 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56441118 | CTCAGCCTCCCAAGT[A/C]GCTGGGAACACAGGC | 57091 |
rs565171779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56448383 | CTGCTTTGCTCTCCT[C/T]CCCCTGGTCCTGACC | 57091 |
rs565221210 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56429905 | GTATTTTATTTCTCA[A/T]AACTTCTTGTATTTT | 57091 |
rs565228542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56435631 | ACTTTTTTTAGAACT[C/G]TGTGGCTAACTGAAA | 57091 |
rs565234872 | in-del | -/AAAC | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56438864 | CTCCATCTCAAAAAT[-/AAAC]AAACAAACAAAAAAC | 57091 |
rs565384878 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56458216 | AGTATTGGGCTTCCC[A/G]AACCAAACCATGCTT | 57091 |
rs565395698 | snp | C/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410010 | AAAGCCTATTACTTT[C/T]GTGTCTTACTTTTCT | 57091 |
rs565454391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56415972 | TGGCCTCAAAGGTGG[C/T]AAATTTAACACCTCA | 57091 |
rs565496229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56439626 | AGCTGCAGAGAGCTA[C/T]TATTACTACGGCGCC | 57091 |
rs565506984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56454729 | GAAAACAAAGACTTA[A/G]GAACCATGGTAAGCT | 57091 |
rs565812713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413910 | GGTACTTTGTCATAT[C/T]TGTGTGCATTTATTT | 57091 |
rs565920415 | snp | G/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410379 | CAGGAATTGAAAGAG[G/T]ATTACTTTTTGAAAT | 57091 |
rs565945454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56426107 | CTAAGATGTCCACAC[C/T]GTCTTGTGATAGAGT | 57091 |
rs566038362 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CASS4 | GRCh38.p7 | 20:56434557 | TTCTTCTGCCTCAGC[A/C]TCCCAAGTAGCTGGG | 57091 |
rs566114748 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409578 | CAATTTTCCTCCCTA[C/T]GCATGTATAAGGCAC | 57091 |
rs566222126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56429306 | CCTTCTCTGCAGTTA[C/T]GCTCCTGCTCTTCTT | 57091 |
rs566247213 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56431120 | TTAGAATTTAAGTGA[-/C]CTTGGACAAGTCATT | 57091 |
rs566450541 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56448519 | CTCAAGTCATTGAAT[C/G]GTCCCATGGGAACAC | 57091 |
rs566466249 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417789 | TCCTGACTCTCAGCT[C/T]TCTAACCCCTACCTG | 57091 |
rs566745341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56430071 | AGCCCCTGGAATACA[C/T]GTGATGCTCAATACA | 57091 |
rs566807244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56430691 | TCCCTGCACGCCCAG[A/C]CTGACCATAACAGCC | 57091 |
rs566852493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56423763 | TTGGCCAGGCTGGTC[C/T]TGAACTCCTGACCTC | 57091 |
rs567055091 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441129 | AAGTAGCTGGGAACA[C/T]AGGCTCCCACCACCA | 57091 |
rs567139257 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438044 | TCTATATTCCCAGTA[A/C]TCTGGGGGGACGAGA | 57091 |
rs567147058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420517 | CCTCAGCCTCCCAAG[C/T]AGCTGAGACTACTGG | 57091 |
rs567269447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414892 | ATAAATAGTAGCCAA[C/T]CCTTACCGATTGTCT | 57091 |
rs567280297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56454302 | AGGCCCAGAAGTCAC[C/T]TGGGGGCTGTGTCAA | 57091 |
rs567431213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56455026 | AATAGGACTGACTCC[A/G]TTCCTCTTTGACATT | 57091 |
rs567507715 | snp | C/T | 2.74729e-05 | 0.00370617 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458755 | TGGGATGAGGACTGT[C/T]TACCTCCCTTCCTCC | 57091 |
rs567535103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56436317 | ATGTATACACAATAT[A/G]TAATGGATTGCTATA | 57091 |
rs567569668 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459442 | CTTATAGGGCTAGCT[C/T]GGTTCTTCTTCAATG | 57091 |
rs567575284 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428918 | GCAATCAGTGTACCC[C/G]CCGACCTGCCCCCCA | 57091 |
rs567591153 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441435 | CATAGTGAAACCCTG[C/T]CTCTACTAAAAACAC | 57091 |
rs567613648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56423718 | CCCGGCTAATTTTTG[C/T]ATTTTTAGTAGAGTC | 57091 |
rs567720724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56416349 | GCCACTGCGCCCAGC[C/T]AGAAATTTAGTTCTA | 57091 |
rs567807628 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420464 | CGTTATCATAGTTCA[C/T]TACAACCTCAAACTC | 57091 |
rs567808637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417021 | TCAAGAAGGATCAAG[A/G]TAAAAATGTAGAATT | 57091 |
rs567878550 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56455823 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 57091 |
rs567900089 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56420837 | CAGCCACTGGGAGTC[-/AG]GGCCAGTTACATAAG | 57091 |
rs567919092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444583 | AGTTCAGGAGGTCTG[A/G]GTGGGAGACTTGGCA | 57091 |
rs567989407 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56430026 | GCATGAGATCAGAAA[C/G]AGTTTTGTTCACCAC | 57091 |
rs568078807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438010 | TATATTCCAGGCTGG[G/T]CATGGTGGCTTACAC | 57091 |
rs568097945 | snp | C/T | 1.89234e-05 | 0.00307593 | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412455 | GCTGCTCCACATCAC[C/T]GACATGAAGGGAACA | 57091 |
rs568190137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424557 | ACCAGCCTGGCCAAC[A/G]TGGGGAAACCCCGTC | 57091 |
rs568202766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56432080 | GATCGTTGAGGATAC[G/T]TGTCCAACTTGAATG | 57091 |
rs568254800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56450490 | ACCGAAAAGTCTTCA[A/G]GAATTTGTGTCTTCC | 57091 |
rs568274762 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56450067 | ATGGAGTTTCGCTCC[C/T]GTTGCCCAGGCTGGA | 57091 |
rs568335378 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56444267 | AGTCCTCAGAAACTG[C/G]TCCTCTGCCTGCGTT | 57091 |
rs568416698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451251 | GGACAGTGCCTGGCA[C/T]GGTGTGAAATTATGT | 57091 |
rs568474802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445541 | GTCCCTAGAGAACAT[C/T]GGAATCACCTGGCAA | 57091 |
rs568557644 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450394 | GAAAAAGGACTGTGA[C/T]GTCCCCTGCGTTGCC | 57091 |
rs568570360 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455758 | AACATGGTGAAACCC[C/T]GTTTCTACTAAAAAT | 57091 |
rs568773419 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56436995 | CACTTAGACCCCAAG[G/T]ATGTGAAGGAACAAA | 57091 |
rs568820933 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448594 | CGCACCCCATTTCCC[A/G]GCTGAGGAGAGCCCT | 57091 |
rs568823490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450038 | TGAGAGGTCTTTTTT[A/T]TTTTTTCTTTGAGAT | 57091 |
rs568823590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443539 | GGCTTGTCCACCTAG[A/T]CCAATCAGCCTGAGA | 57091 |
rs568845072 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420895 | ATCCCAAATAAGGAC[C/T]GGGGTGGGTTTATGT | 57091 |
rs568879246 | in-del | -/CC | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56431113 | AACCAATTAGAATTT[-/CC]AAGTGACCTTGGACA | 57091 |
rs568972156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56430829 | AACAGCAAAGAAAAG[A/G]TCTGAGGTGGAAGCA | 57091 |
rs568976586 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411542 | ACAGAGAAAGACTCC[A/G]TCTCAAAAAAAAAAA | 57091 |
rs569086751 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409668 | TGTTCTTGATAGCAC[A/G]TTTGCCAAGAGCATT | 57091 |
rs569132810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56423806 | CACCTCGGCGTCCCA[A/G]AGTGTTGGGATTACA | 57091 |
rs569161981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56449287 | TGCAGCCATAAAAAA[C/T]GATGAGTTCATGTCC | 57091 |
rs569169596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417112 | AAGTGTGTACCACTT[G/T]CTGGGACTTGGCTTG | 57091 |
rs569201811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456246 | ATGCGATAACCAAAA[C/T]TATCTCCACACATTT | 57091 |
rs569206263 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411820 | AAAGACCAGGAGATG[A/G]GCATGGGGTTCCGAG | 57091 |
rs569249104 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411229 | CCTGGCTTGGAAGAA[C/T]GGGCACCATTTTGTC | 57091 |
rs569265583 | snp | A/T | 8.40301e-05 | 0.00648136 | intron-variant | CASS4 | GRCh38.p7 | 20:56450695 | GTAAGTATGAAGAGG[A/T]GCTAAGGTGCGGTGT | 57091 |
rs569351938 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436065 | CCTCTTGTCATTCAC[G/T]TATTAATGAACATTT | 57091 |
rs569463149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56445493 | CTAGATGAATGTAGA[C/T]GAATAGCTCAGTATC | 57091 |
rs569516230 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441269 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCTACTG | 57091 |
rs569528662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438925 | TGTATGTGCATGTGT[A/G]CTCTCACACTGAGAC | 57091 |
rs569560445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56439055 | GTCCTCAGCACGTGG[A/G]ACCAGGCCTGGCCTG | 57091 |
rs569590096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56439537 | AATAATTAGGCAGGC[A/G]TGGTGGCAGGCACCT | 57091 |
rs569696680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56426471 | ACACTCCTTTCAGGG[C/T]GAACAGAATGGTTTT | 57091 |
rs569729268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56419078 | AGACAGGCATTGGCC[A/G]ACACGATAATGGAAT | 57091 |
rs569732835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56457484 | ATAAAATTCATGAAT[A/G]TAAAATTTTGATGAA | 57091 |
rs569816832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56419727 | TGAGCCACCGTGCCC[A/G]GCTAGGCTCTGCACT | 57091 |
rs569877567 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56458159 | TGTATATATTATATA[G/T]TACAGTGCTTTGAAA | 57091 |
rs569950037 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432989 | TACCTCTTAAAGACT[G/T]GAAAATGGGGGCGTT | 57091 |
rs570049460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433465 | TGATGGTTTGGGCAC[A/C]GTTTGGGCTTTGTCC | 57091 |
rs570142886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56434273 | ATATTAGCTATAAAG[A/G]TGATCATTTCAGCAT | 57091 |
rs570249871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413106 | ACCGGAGAGGCTGAG[C/G]TGAGAAGATTAATTC | 57091 |
rs570282121 | snp | C/T | 1.77269e-05 | 0.0029771 | intron-variant | CASS4 | GRCh38.p7 | 20:56450564 | CCATTAGGAAAGAAA[C/T]ATTCAAGTTGTCTGC | 57091 |
rs570724186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438087 | TTGAACTCAGAGTTC[A/G]GGACCAGCCTGGGCA | 57091 |
rs570860378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56439651 | GGCGCCCCTGCACTC[C/G]AGCCTGGGTGACTGA | 57091 |
rs570893782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56446309 | TTGACCAGGCTGGTC[C/T]CGAACTCCTGGCCTC | 57091 |
rs570911451 | in-del | -/A | 0.462034 | 0.132445 | intron-variant | CASS4 | GRCh38.p7 | 20:56447207 | GCAAGACTCTGTCTG[-/A]AAAAAAAAAAAAATC | 57091 |
rs570918679 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CASS4 | GRCh38.p7 | 20:56416330 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 57091 |
rs570980329 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436900 | TCAAAACCAAAAACA[A/C]ACAGGGCCATGAAAG | 57091 |
rs570990480 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56428757 | GGACTTGGAAAGGCC[A/C/G]TGCAGAGTATTGGCA | 57091 |
rs570991442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56456887 | AGACAGAGTTTCGTA[C/T]GTTGCCAAGGCTAGT | 57091 |
rs571000465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56447080 | GGGCATGGTGGTTCA[C/T]GCCTGTAGTCCCAGC | 57091 |
rs571011329 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56412584 | TAGTTGTGACTTTCT[A/G]ATAAAGGTTGAATAC | 57091 |
rs571184962 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452869 | GAGAGGTTTGTCATG[A/G]TGGCACGGATGCTTC | 57091 |
rs571194072 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56427733 | TCTGTGATATTTATA[A/G]TATATGCAGTTTTTA | 57091 |
rs571250552 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459418 | TGTGTGCCCTCTCAT[A/G]TGCAATTCCTTATAG | 57091 |
rs571310846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56453304 | AAATCTTATTAACAA[A/G]TCAGATAAAGATAGG | 57091 |
rs571413631 | in-del | -/T | | | splice-donor-variant | CASS4 | GRCh38.p7 | 20:56450680 | ACAGCCAAGCAAGTG[-/T]TAAGTATGAAGAGGT | 57091 |
rs571513593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56428856 | AGGCAGGTCATTAAT[C/G]TCTCCTAGTCTTAGG | 57091 |
rs571519281 | snp | A/T | | | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453085 | AGGGAAGATGAACAC[A/T]CTTCTGAACTATTAA | 57091 |
rs571522140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56442142 | CACGGACTCCTTTCT[A/G]TATCTGTGTTGACAG | 57091 |
rs571578142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56436053 | CACTGCGCCCAGCCT[C/T]TTGTCATTCACTTAT | 57091 |
rs571606560 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56442656 | TTAATATAATGTGCT[A/G]GCCTAATTTAAAAAA | 57091 |
rs571689913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56457586 | AGGTCAGGGTATTTA[C/G]TTGCTTCTGGAAATG | 57091 |
rs571751919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451731 | GAGCCACTGAAGGAG[C/G]GGCGGAGTGACGATG | 57091 |
rs571794274 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56415664 | CAGTGGTCCTTAGCT[G/T]TGGGGCATTCGCCTT | 57091 |
rs571796043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56422751 | CAATGTTATCATGGA[G/T]AACCAGTTAAAGTTT | 57091 |
rs571865341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56432556 | ATTTTTTGGTAGAGA[C/T]GGGGTTTCACCATGT | 57091 |
rs571907952 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414149 | ATTCAGTCTAATTCA[C/T]GTTGATTTAATAATG | 57091 |
rs571912116 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447319 | AAACTTTCTAGTTCA[C/T]TTAAAGCTAAAGCTC | 57091 |
rs571946753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417429 | GCCTCTCTGGACCAC[A/G]CTGTGCAAATCACTT | 57091 |
rs572166702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56425639 | GAAAGGGCTTGCGTG[A/G]TAACGACAAGCAGCT | 57091 |
rs572182343 | in-del | -/TTAT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434437 | ATGCTCACAATTTAC[-/TTAT]TTATTTATTTATTTG | 57091 |
rs572354034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420156 | AGAGAGTTTCTCCAC[A/G]AGTTTATGTTAGTGA | 57091 |
rs572400550 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | CASS4 | GRCh38.p7 | 20:56412271 | CTTTCATTTTACTCT[C/T]ATCGTGCTTTCCAGA | 57091 |
rs572428465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56427097 | GACCAGGAGTTTAAG[A/G]CTGTAGTGCACCATG | 57091 |
rs572494030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56428200 | AATTTTAGGAGCATA[A/G]GTGTTTGGTGTCAGG | 57091 |
rs572500435 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427030 | GCTAGGCATGGTGAT[A/G]TGTGCCTGTAGTCCC | 57091 |
rs572530693 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414334 | TTTCATAACATTGAC[C/G]TTTTTTCTAAACAGC | 57091 |
rs572594122 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458810 | CCACAACTTGTGCAA[C/G]TCTGCCCTATGGGAA | 57091 |
rs572652711 | in-del | -/TTTA | 0.00159617 | 0.0282053 | intron-variant | CASS4 | GRCh38.p7 | 20:56423540 | TAAACATTACTTTAT[-/TTTA]TTTATTTATTTATTT | 57091 |
rs572772656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433487 | GCTTTGTCCAAAGGG[C/T]AATAGGGAGCCACTG | 57091 |
rs572789427 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56418724 | AGTGGTTGTGAGCAG[-/A]AAAAAATAGTAAATC | 57091 |
rs572794859 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412209 | TGAGACGTCAGGCAT[C/T]GAGACGTGAGTGTGG | 57091 |
rs572843296 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56445097 | CCTGGGCAACAGGAG[C/T]GAAGATCCATCTCAA | 57091 |
rs572849863 | snp | A/G | 0.173965 | 0.238157 | intron-variant | CASS4 | GRCh38.p7 | 20:56436336 | TGGATTGCTATATAT[A/G]TGTGTGTGTGTGTGT | 57091 |
rs572878016 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414580 | CCGAGCCCCACTGCA[A/G]TTTGTAAATAACATG | 57091 |
rs572887423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56448973 | AACAGGTGCTGGAGA[A/G]GATGTGGAGAAATAG | 57091 |
rs572949104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56449419 | AACAATGAGAACACT[G/T]GGACACAGGGTGGGG | 57091 |
rs573057697 | snp | A/G | 1.65485e-05 | 0.00287645 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453050 | AATCACACCAAAAGA[A/G]TACCCCTTCCACTAA | 57091 |
rs573105273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56422345 | GAGACCTTTATTGTT[A/G]CATCATTTCAATCCT | 57091 |
rs573164189 | snp | C/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409964 | CAAACTAGGTATCTA[C/T]GTAGGAGCTAGTTGA | 57091 |
rs573185794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56448002 | AAAAAGTTAGCCGGG[A/C]ATGGTGGCAGGTGCC | 57091 |
rs573222718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56454697 | AAGATAAACCTATCT[C/T]GGAATAAAGGTTAGA | 57091 |
rs573272469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56440806 | CAAACAACAGAAACC[A/G]CAAGGAAATTCAGGG | 57091 |
rs573297294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443730 | GTGCACAACACGGCA[C/G]CGTGCAGGCTGGACG | 57091 |
rs573331680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56441450 | TCTCTACTAAAAACA[C/T]AAAAATTAGCCATGT | 57091 |
rs573745267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56454574 | AATATGAGAAAGAAT[A/G]CTCAAGTCTAAAGTG | 57091 |
rs573829430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421611 | TGAGGTGGGAGGATC[A/G]TTCGAGCCCAGGAGT | 57091 |
rs573830059 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424598 | ATACAAAAATTTGCC[A/G]GGTGTGGTGGCATGC | 57091 |
rs573862063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446649 | CCATCCAAATGCTCT[G/T]CGGTGGCGTTCTCCC | 57091 |
rs573881231 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452925 | CATTGTCATTGCCAA[C/T]GGAAGGCTCCTTTTT | 57091 |
rs573929424 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56456199 | CATCCCAGAACCCCT[G/T]CCCGCTCACTGCCTA | 57091 |
rs573938212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56453952 | TTGGGAGGCCAAGGC[A/G]AGCAGATCACTTGAA | 57091 |
rs573996335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56448264 | TGACATTTTGTTCAC[C/T]ATGATTTTTTTGCAT | 57091 |
rs574018259 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459799 | TTCACTCATTTAACA[C/T]TTATGTATTGGATGC | 57091 |
rs574019136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56449172 | CACGTATGTTTATTG[C/T]GGCACTATTCACAAT | 57091 |
rs574062174 | in-del | -/AAG | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418740 | AAAAAATAGTAAATC[-/AAG]GAGTAGATAGCTTCT | 57091 |
rs574106873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56428468 | AGGAAATCTGGATGG[A/G]GTCTCTAAGACCTCA | 57091 |
rs574158995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420880 | AAGCCCCCTTTGGGT[A/G]TCCCAAATAAGGACT | 57091 |
rs574285109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56422323 | AATCAATTATGTGAA[A/G]GCCTGAGAGACCTTT | 57091 |
rs574381179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56423268 | GAATGTGAGTATCTG[A/T]GTTTCTGTCTTCTGA | 57091 |
rs574442712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56430263 | TCTCTTATTCTTCAC[A/G]TTTGTTTCCCTATCC | 57091 |
rs574518714 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56449367 | TGCAAGGACAGAAAA[C/G]CAAACAACGCATGTT | 57091 |
rs574523494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438363 | GAAATATACAAGCAG[A/G]CAAATATATGTCTGG | 57091 |
rs574624073 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456830 | ACTACAGGCCCGCAC[C/T]GCCATACCTGGCTAA | 57091 |
rs574639200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56429741 | ACTCCTTATCTAACT[C/T]CTCCTTACCCCCAGA | 57091 |
rs574711954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444972 | AAAATTAGCCTGGCA[G/T]GGAGGCATGTGCCTG | 57091 |
rs574716580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56436573 | GTAGCTAATTTGCTT[A/G]AAGGTACACAGGTAC | 57091 |
rs574780174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56437061 | AAATGAAATGAAAGG[A/G]CATGATGAATTTGTA | 57091 |
rs574783713 | in-del | -/AGGG | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433491 | TGTCCAAAGGGTAAT[-/AGGG]AGCCACTGAAGGGTG | 57091 |
rs574802033 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56453371 | TTCCGAAAACTTTTG[A/G]CGTTCAAGTTTACCA | 57091 |
rs574993795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56422469 | GCCTTAAGTGCAGCT[C/T]AGCAAGGTTTCCATG | 57091 |
rs575043057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450750 | AAATGTTATTAGCTT[C/G]GGGCCAGGCACGGTG | 57091 |
rs575086284 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444399 | ACTCCCCCTGTCCTG[G/T]ACTCCGGAGCTTCAC | 57091 |
rs575125059 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442605 | ACTAGGGTAACCACT[A/G]TCTTGAGCTTTGTTT | 57091 |
rs575198425 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454192 | TCTCAAGAACAACAA[A/C]AACAAAAAAACAAAA | 57091 |
rs575203083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56443855 | GAATCAAGGCTGCTT[C/T]TCTGTCAATGACTCA | 57091 |
rs575242884 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418082 | GGGGGTTCAGGGTGA[C/T]CAAGACAGAGCTGAC | 57091 |
rs575265549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56444346 | CTTGGAAAGCCCCCT[A/G]CTGAGCAACAGCTCC | 57091 |
rs575304422 | in-del | -/AAAT | 0.00160707 | 0.0283011 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410742 | ACTCCGTCTCAAAAA[-/AAAT]AAATAAATAAATAAA | 57091 |
rs575438307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56435698 | CCTGGCTTTGTGACC[A/G]CAGGCAAGTCACTAA | 57091 |
rs575452433 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415376 | AACACCCAAGTTGTC[A/G]ACACCTAGTTCAGAG | 57091 |
rs575473706 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56448078 | ACCCGGGAGGCGGAG[C/G]TTGCAGTGAGCAGAG | 57091 |
rs575598035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56443086 | GGGAGAAAGCTTGGT[A/G]TGTTTCTGGGAGGTA | 57091 |
rs575696891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450286 | GCCTCAGCCTCCCCA[A/G]GTGTTGGGATTACAG | 57091 |
rs575720850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56415633 | TAGCACAATGCTTCA[A/G]GGGGTCATGTCATGT | 57091 |
rs575855359 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409785 | CCCAGTTTCCTAGAC[A/T]AATAGTTCTTGCAAT | 57091 |
rs575896034 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410695 | AGTGAGCCGAGATTA[C/T]ACCACTGCACTCCAG | 57091 |
rs575905390 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | CASS4 | GRCh38.p7 | 20:56456690 | CCCTTTTTTATTTTA[-/T]TTTTTTGAGACAGTG | 57091 |
rs575969082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456435 | TGGGAGTGCAGTGGC[A/G]TGATCTCAGCTCATT | 57091 |
rs575995082 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56456937 | GCGATCCTCCTGCCT[C/T]GGCCTCCCAAAGTGC | 57091 |
rs576027453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56450907 | GGTGTGGTAGTGGGC[A/G]CCTGTAATCCCAGCA | 57091 |
rs576130037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56418626 | CTGCTCTTCTCCATG[C/G]ACACGAAGGAGAATC | 57091 |
rs576139930 | snp | A/C/T | 0.004783 | 0.0487016 | intron-variant | CASS4 | GRCh38.p7 | 20:56429447 | CAATTGACTTTGAAT[A/C/T]GCCTCTCTGGCTTCC | 57091 |
rs576171541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56431612 | GCTATTCATCTTGGA[C/G]AGCTGTGAGTGCCCA | 57091 |
rs576311869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56433140 | GTTCTTATGGGGAGA[C/G]AGACCCTGGATGAGT | 57091 |
rs576321926 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56446311 | GACCAGGCTGGTCTC[A/G]AACTCCTGGCCTCAA | 57091 |
rs576374996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56426305 | TACCTGCTTCATAAG[G/T]TTTTTGAATATCAAA | 57091 |
rs576439358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56418003 | CAGACACAACACCCA[A/C]CTCGAAAACACAGCT | 57091 |
rs576537563 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56451413 | ACAGACACACTTACA[A/C/T]CCAAGGTCATTAGGG | 57091 |
rs576571949 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454242 | CTGGATGAGTTCAGA[C/T]ATTATAGAGCGAGAT | 57091 |
rs576573783 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56422110 | AAGGGTGAAATTGTC[A/T]GCCCCTTGACTTGAT | 57091 |
rs576631931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56457826 | TCAAAACCAATCTGG[C/T]CAACATGGTGAAACC | 57091 |
rs576739384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56439129 | AGTTGATTTTTATGT[C/G]ATATTGAACATGTAT | 57091 |
rs576739832 | snp | A/G | 3.43359e-05 | 0.00414328 | intron-variant | CASS4 | GRCh38.p7 | 20:56446006 | TGGTCCTGAAGGTGA[A/G]CCTTGTTCAGGGGCC | 57091 |
rs576775059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56417369 | TCCCCTGCTGTTCCC[C/T]GCCTTGGATTCTTCT | 57091 |
rs576802402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56439797 | TGGCCTTCATGAGGT[A/G]TTGAGATGTAGAGCA | 57091 |
rs576813598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56456111 | CTTTAGACTGACAGC[A/T]CTTCTCAGTGGAGGC | 57091 |
rs576872812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424155 | TGCAAGAAACTACTT[A/G]GCTATCACCTCATTA | 57091 |
rs576892037 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411507 | AGCCGAGATTGCGCC[A/G]CTGCGCTCCCACCTG | 57091 |
rs576924301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56425790 | GAACATGGACTCAAA[C/G]TGTTTTTATCTAATC | 57091 |
rs576936827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56424714 | CCACTGCATTCCAGC[C/T]TGGATGACAGAGCGA | 57091 |
rs577091055 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433849 | TCACAATACACATGC[C/T]CCTAACTCCTTTGGG | 57091 |
rs577181588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56446133 | CCAGAATACACATCA[A/C]CACTCAGAGGCCAAC | 57091 |
rs577207670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56430901 | GAGGGAAATGAATGA[A/G]GGTAGAGCTGCAAAC | 57091 |
rs577245958 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CASS4 | GRCh38.p7 | 20:56446506 | TATCACTGATTATCT[C/T]AACATTGATTATCTC | 57091 |
rs577380036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56418749 | TAAATCAAGGAGTAG[A/G]TAGCTTCTATTTATG | 57091 |
rs577395858 | snp | A/G | | | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458819 | GTGCAACTCTGCCCT[A/G]TGGGAAAAGCCAGCC | 57091 |
rs577417602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56419302 | ATTTCCAAACATAAC[A/G]CCTATGAAGTGTTTG | 57091 |
rs577455982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56438421 | AGAAAACTCAAAGAG[A/G]CCTAAATGTTTATTA | 57091 |
rs577479252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56450800 | GCACTTTGAGAGGCC[A/G]AGGTGAGTGCATCAC | 57091 |
rs577521396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CASS4 | GRCh38.p7 | 20:56421103 | TTTCTCTGTCATGCA[C/T]TAAACAGCTTGAGCC | 57091 |
rs577521413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451759 | ATGAGATTTAAACAA[C/T]GCACTCGCGCCCTCT | 57091 |
rs577559440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56451283 | ATGGCTTCTTCTTAC[A/G]ACAGACCTCAGGGGC | 57091 |
rs577798475 | in-del | -/ACTT | 0.00517822 | 0.0506191 | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409618 | GAATTGGTCAGACTC[-/ACTT]GTCTCAGAAAAGAAA | 57091 |
rs577897267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56413355 | TGCTTATAAAAATCA[A/G]TGCTTATTTTTCATT | 57091 |
rs577934006 | snp | C/G | 0.00398564 | 0.0444627 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458887 | CAAAGCTGGTAGTAC[C/G]AAGTGGCTAAGCAAC | 57091 |
rs577977811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56414515 | AATTCCTGAACTCAG[A/G]TGATTCTTCTGCCTC | 57091 |
rs578041118 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CASS4 | GRCh38.p7 | 20:56415110 | GAGCTCCATTCTTAG[C/G]TCATTATATTCTCTC | 57091 |
rs578069694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56421344 | TTTACCTAAAAAATT[A/G]TAGTGGCACGTGGAT | 57091 |
rs578134001 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CASS4 | GRCh38.p7 | 20:56453679 | GGATCCCTTGAGGCA[A/G]GAGTTTGAGACCAGG | 57091 |
rs578134639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56434645 | AGAGATGGGGTTTCA[C/T]CATATTTGCCAGGAT | 57091 |
rs578226162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56427291 | TTTGATTTTTCCTCA[C/G]GTTGTCCTTCCTCCT | 57091 |
rs578243781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56428306 | GAGAAGGAGCTGGAC[A/G]GAGTAGAGACAGCCT | 57091 |
rs578259317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CASS4 | GRCh38.p7 | 20:56420760 | AAGAGTCAGTAATCA[A/G]TAACAAACAACTCAA | 57091 |
rs745327778 | snp | A/G | 1.65214e-05 | 0.0028741 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56445941 | CCGGGCCTCACTGCC[A/G]ACTCTGCCTTCCCAG | 57091 |
rs745383088 | snp | G/T | 1.72653e-05 | 0.00293809 | intron-variant | CASS4 | GRCh38.p7 | 20:56445875 | GACATTTCCTTTTCC[G/T]CTTTTCTCCTCCTTT | 57091 |
rs745392746 | snp | A/G | 1.67041e-05 | 0.00288994 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452511 | CAAGGAGACAGTGAT[A/G]GCTCTGCAGCACAAG | 57091 |
rs745411263 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413511 | AACCCCATATCTACC[A/G]AAAATACAACAATTA | 57091 |
rs745458228 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433270 | GAAGTGACATTTAAG[A/G]TAAGCCTGAAAGGAT | 57091 |
rs745520032 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432430 | TGTAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG | 57091 |
rs745625249 | snp | A/G | 3.29647e-05 | 0.00405971 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452055 | GTCCCTCACTCCACA[A/G]CTGAATAACAATGTG | 57091 |
rs745649411 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425045 | GCAGCTACTGTGTCC[C/T]GATACTGCATATCCT | 57091 |
rs745662902 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438003 | TAAAATGTATATTCC[A/G]GGCTGGGCATGGTGG | 57091 |
rs745664879 | snp | A/G | 1.92228e-05 | 0.00310017 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453116 | AGAAAAATAGGGCAA[A/G]TATCTGTGGACAGGT | 57091 |
rs745667936 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443207 | GGATTTCTGGCCTGG[C/T]GCGGTGGCTCACGCC | 57091 |
rs745730930 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56412798 | ATGCGAGTCTGCCTC[A/G]GCCCCCGCTAATTCC | 57091 |
rs745768861 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457371 | TTCTCTGAGCTTCAC[C/T]TTTCAATTGTTACCT | 57091 |
rs745826641 | in-del | -/TGAA | 0.000280854 | 0.0118469 | intron-variant | CASS4 | GRCh38.p7 | 20:56412515 | TGATGTGGGGCTGTT[-/TGAA]TGGGCTCTGGCGGGG | 57091 |
rs745844917 | snp | A/C | 1.65258e-05 | 0.00287448 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452193 | CTTTCTGATTCCCCG[A/C]GTGGAACAGCAGAAC | 57091 |
rs745845431 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441953 | CACAGAAAAGGCAGG[C/T]GTCTCCTCCCTGCTC | 57091 |
rs745886142 | snp | A/G | 1.66916e-05 | 0.00288886 | intron-variant | CASS4 | GRCh38.p7 | 20:56450686 | CAAGCAAGTGTAAGT[A/G]TGAAGAGGTGCTAAG | 57091 |
rs745893482 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452884 | GTGGCACGGATGCTT[C/T]CAGAAGACATCAAGA | 57091 |
rs745957282 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438375 | CAGGCAAATATATGT[A/C]TGGATGAGGAGGCTG | 57091 |
rs746052282 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56451021 | TAAAATACAAAAATT[A/T]AAAAAAAAAAAAAAG | 57091 |
rs746086661 | snp | A/C | 5.66032e-05 | 0.00531963 | missense | CASS4 | GRCh38.p7 | 20:56412459 | CTCCACATCACCGAC[A/C]TGAAGGGAACAGGCA | 57091 |
rs746138167 | snp | C/T | 1.73996e-05 | 0.00294949 | intron-variant | CASS4 | GRCh38.p7 | 20:56451801 | CTAACCCGGCAACTA[C/T]GTGTGGTTCTCCCAC | 57091 |
rs746148078 | snp | A/G | 0.000204303 | 0.0101049 | intron-variant | CASS4 | GRCh38.p7 | 20:56437123 | GCAGTCACTGGCCAC[A/G]GTGCTAACTGCAAAT | 57091 |
rs746192245 | snp | A/C/T | 6.59635e-05 | 0.00574265 | missense | CASS4 | GRCh38.p7 | 20:56458574 | CAGGAGAGGGACGTG[A/C/T]GCAACGAGATCCTCC | 57091 |
rs746316839 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442703 | AGAGCATATTTGATT[C/T]CAGTTTAAATTCAGA | 57091 |
rs746331913 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429032 | AGCTGTGCATGTGGG[C/T]GAGTGCACGTGGGTG | 57091 |
rs746393684 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441520 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAAG | 57091 |
rs746506073 | snp | C/T | 2.02177e-05 | 0.00317938 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453121 | AATAGGGCAAATATC[C/T]GTGGACAGGTGAGTT | 57091 |
rs746546964 | snp | C/G/T | 3.5409e-05 | 0.00420755 | intron-variant | CASS4 | GRCh38.p7 | 20:56446023 | CTTGTTCAGGGGCCC[C/G/T]TCATCACCCAGACCT | 57091 |
rs746554650 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424983 | AGGAGGAAAGTAGGG[A/G]CATGGTTATTCTGAA | 57091 |
rs746560893 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411662 | GCAAGTGATGATAAA[C/T]TGCATGAGCTAGCAG | 57091 |
rs746623264 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445201 | TCACTGACCTGCTCC[C/T]TGTTAACCTTTCCCA | 57091 |
rs746650344 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457218 | TATGCCCTATCTGTC[C/T]GAATGCTTCCGGGCT | 57091 |
rs746705363 | snp | C/T | 1.67181e-05 | 0.00289115 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458348 | TCTTTAGAATCCTGG[C/T]CCTCTTATACCTCAG | 57091 |
rs746727406 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452073 | GAATAACAATGTGCC[C/T]ATGCAGAAAAAACTC | 57091 |
rs746762411 | snp | C/G | 3.40872e-05 | 0.00412825 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437455 | CGCCCTCCCACTCCA[C/G]GCCCCGTTTATGAGC | 57091 |
rs746817385 | snp | A/C | 1.65343e-05 | 0.00287521 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452200 | ATTCCCCGAGTGGAA[A/C]AGCAGAACACCAAGC | 57091 |
rs746834012 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56449919 | ATTAGGTCTCAGTCT[C/T]ATTTATCCTCTGGCT | 57091 |
rs746911012 | snp | A/G | 0.000128199 | 0.0080052 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56437178 | GGCACTCCTGGCCAG[A/G]GCACTTTATGACAAC | 57091 |
rs746922024 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436011 | CCCTCCTCGGCCCCC[C/G]AAAGTGCTGGGATTA | 57091 |
rs746992689 | snp | A/C/T | 5.29818e-05 | 0.00514671 | intron-variant, synonymous-codon | CASS4 | GRCh38.p7 | 20:56437496 | TTGGGCGGAGGGGCC[A/C/T]CAGCCCCCTACTGCC | 57091 |
rs747015969 | snp | C/G | 1.90141e-05 | 0.00308329 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56412473 | CATGAAGGGAACAGG[C/G]ATCATGGACTGTGCG | 57091 |
rs747104129 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427526 | CCAAGTACATTTGAA[A/G]GGAGACTATTTACTT | 57091 |
rs747222178 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447756 | TGGCTCTTGCTCCAG[A/C]TCTTGTGTGAGCCAT | 57091 |
rs747288992 | snp | A/G | 1.6498e-05 | 0.00287206 | missense | CASS4 | GRCh38.p7 | 20:56458580 | AGGGACGTGCGCAAC[A/G]AGATCCTCCGTGGCA | 57091 |
rs747356655 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421048 | AAAATTACCATAGAA[A/C]GATGGAAAAGTTTGG | 57091 |
rs747377046 | snp | C/G | 1.75832e-05 | 0.00296501 | missense | CASS4 | GRCh38.p7 | 20:56458661 | GCCGTGCTCACGTAC[C/G]CCAGCCCTGCCGCGC | 57091 |
rs747432969 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454947 | ATGAAAGTGAAGCAT[A/T]AACCATTACTGAAAT | 57091 |
rs747506729 | snp | C/T | 1.65647e-05 | 0.00287786 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56445965 | TTCCCAGGTGTATGA[C/T]GTGCCTACCCAGCAC | 57091 |
rs747531773 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56453857 | CCAGCCTTGGTGACA[C/G]AGCAAGAGCTAATCT | 57091 |
rs747621928 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452619 | TGATGCAATCCACAG[A/G]TCCACTGATCACATA | 57091 |
rs747639942 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458453 | CAAAGCCATCAGCGC[A/G]TTTCACGGCAGCCTC | 57091 |
rs747666778 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447960 | ACCCTGGCTAACGCG[A/G]TGAAACCCCGTCTCT | 57091 |
rs747700865 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421310 | GGACAGTTGTTTTTT[A/G]ATTGACTCAATTTGT | 57091 |
rs747708829 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435820 | CAGTGGCATGATCTC[A/G]GCTCATTGCAACCTC | 57091 |
rs747726001 | snp | A/G | 4.98674e-05 | 0.00499312 | missense | CASS4 | GRCh38.p7 | 20:56458357 | TCCTGGCCCTCTTAT[A/G]CCTCAGCCTTCGAGT | 57091 |
rs747737427 | in-del | -/AAG | 1.65844e-05 | 0.00287957 | cds-indel, intron-variant | CASS4 | GRCh38.p7 | 20:56451854 | ATCAGTGACTACCTT[-/AAG]AAGAGGCGGTTACAG | 57091 |
rs747825213 | snp | A/G | 1.66735e-05 | 0.00288729 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452305 | GTGTCAGAGAATTCC[A/G]CGGGCCATAATTCCT | 57091 |
rs747911000 | snp | A/T | 1.78701e-05 | 0.0029891 | intron-variant, synonymous-codon | CASS4 | GRCh38.p7 | 20:56437508 | GCCCCAGCCCCCTAC[A/T]GCCCAAGTCTATGAA | 57091 |
rs747926780 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415934 | ATTTTTTTAAAACAC[A/G]TGATATTAGTGATAG | 57091 |
rs747978501 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414968 | ATTACATCCTCACAA[C/T]ATCCTCATGAAGCAG | 57091 |
rs748042186 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447666 | CTCCTCTGGCTGCTG[C/G]CTCCTCCCTTAGCTC | 57091 |
rs748050844 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434754 | CGGTCCCACAATTTA[G/T]TTTTAAGTGGGAAAA | 57091 |
rs748075982 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56449781 | TGTTTTTATTGCTGT[C/T]GTGATGTGCACAGTG | 57091 |
rs748193269 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452041 | AGTGGCAGATCCAGG[C/T]CCCTCACTCCACAAC | 57091 |
rs748199208 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418315 | TAGTACAGGGCCCCT[A/G]TAAAGACCCATGGGG | 57091 |
rs748199976 | snp | C/G/T | 3.32769e-05 | 0.00407892 | missense | CASS4 | GRCh38.p7 | 20:56437326 | CTGGCCCCTGCCAAC[C/G/T]GCCTCCAAATCCTCA | 57091 |
rs748232416 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438316 | AAGTATATCCCCTTC[A/G]ATGCAGAAATTTTAT | 57091 |
rs748253287 | snp | A/C | 3.6735e-05 | 0.00428557 | missense | CASS4 | GRCh38.p7 | 20:56437174 | CACAGGCACTCCTGG[A/C]CAGGGCACTTTATGA | 57091 |
rs748265528 | in-del | -/CAAA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443090 | AAAGCTTGGTGTGTT[-/CAAA]TCTGGGAGGTACCAC | 57091 |
rs748273238 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415118 | TTCTTAGCTCATTAT[A/T]TTCTCTCCCTTGTAC | 57091 |
rs748293964 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56453656 | CGCTTTGGGAGGCCA[A/G]CGCAGGAGGATCCCT | 57091 |
rs748405041 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439849 | CTGCAGGCATTTCCT[C/G]CCATCAGATGCTTTG | 57091 |
rs748464737 | snp | G/T | 1.77827e-05 | 0.00298178 | intron-variant | CASS4 | GRCh38.p7 | 20:56446027 | TTCAGGGGCCCCTCA[G/T]CACCCAGACCTCTGC | 57091 |
rs748505510 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433236 | TGGTCAAGAGGGTGT[C/G]AGGGACCCTTTTTCT | 57091 |
rs748543994 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418603 | TCATTTTCCACTGGG[A/G]TGGTACCCTGCTCTT | 57091 |
rs748559086 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432123 | AAAAGAGATCATTGA[A/G]GGGCTAGGTAGGTAT | 57091 |
rs748661019 | in-del | -/CA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448141 | AGTGAGACTCTGTCT[-/CA]AAAAAAAAAAAAAAA | 57091 |
rs748695905 | snp | C/G | 1.65737e-05 | 0.00287864 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56450655 | CAAGAAGGCAGGACT[C/G]CATCCCCCAGACAGC | 57091 |
rs748738331 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431802 | TCTAGACAAATGCAA[A/G]CACATTTCAGATGAT | 57091 |
rs748745238 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434399 | TTTAAAGAATATTGA[A/G]AAATGTTTATTGACA | 57091 |
rs748800523 | in-del | -/A | 1.75121e-05 | 0.00295901 | intron-variant | CASS4 | GRCh38.p7 | 20:56446015 | AGGTGAGCCTTGTTC[-/A]GGGGCCCCTCATCAC | 57091 |
rs748813329 | snp | A/G | 1.66649e-05 | 0.00288655 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452307 | GTCAGAGAATTCCGC[A/G]GGCCATAATTCCTCA | 57091 |
rs748815198 | snp | A/C | 1.64787e-05 | 0.00287038 | missense | CASS4 | GRCh38.p7 | 20:56458550 | GTGGACACGCTGTGC[A/C]TGGAGACCCAGGAGA | 57091 |
rs748833068 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421138 | TTGAATTCTTCCGGG[C/T]CAATCAAATGGAAGT | 57091 |
rs748859774 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454078 | TCCAGCTACTCAGGA[A/G]GCTGAGGCAGGAGAA | 57091 |
rs748933567 | snp | A/G | 1.77492e-05 | 0.00297898 | intron-variant | CASS4 | GRCh38.p7 | 20:56445863 | GATCATCAGAGTGAC[A/G]TTTCCTTTTCCTCTT | 57091 |
rs748956463 | in-del | -/GA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420708 | CCCAGGTTCAAAAGT[-/GA]GAGTCTCCCCACGGT | 57091 |
rs749071620 | in-del | -/TCT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426534 | AGGATTTTTCCCTCT[-/TCT]TCTTCTTCTTCTTTT | 57091 |
rs749182154 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414722 | TTCAGAGGCTGAAGC[A/G]TGTGGATCACCTGAG | 57091 |
rs749307548 | snp | G/T | 1.64825e-05 | 0.00287071 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452665 | GAATTTCTGGATTTT[G/T]CCCGAGGAGTCCATG | 57091 |
rs749361560 | snp | G/T | 2.32962e-05 | 0.00341285 | missense | CASS4 | GRCh38.p7 | 20:56458740 | AGTTCAGAGGGACAC[G/T]GGGATGAGGACTGTC | 57091 |
rs749367816 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418497 | GATCTAATTTATGTT[G/T]TCTAGATCACTCAGG | 57091 |
rs749520065 | snp | A/C/G/T | 3.33947e-05 | 0.00408613 | missense | CASS4 | GRCh38.p7 | 20:56437372 | ACAGGCCGTGCCCCC[A/C/G/T]ATTCCTGAGAGGCCT | 57091 |
rs749532978 | snp | C/T | | | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452005 | CTCCCCAGTTCCAGC[C/T]CCACTTTCTACAATC | 57091 |
rs749579321 | snp | A/T | 1.81625e-05 | 0.00301346 | intron-variant | CASS4 | GRCh38.p7 | 20:56446035 | CCCCTCATCACCCAG[A/T]CCTCTGCGCCCAGAG | 57091 |
rs749586658 | snp | A/C | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409887 | TCACACCTTTCATTC[A/C]GAAAAACCATAGAGG | 57091 |
rs749589898 | snp | A/G | 3.29506e-05 | 0.00405884 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452772 | CCGCATCCTGCTTGA[A/G]ACAAAGGAAAGCTTG | 57091 |
rs749613094 | snp | C/T | 1.75434e-05 | 0.00296165 | intron-variant | CASS4 | GRCh38.p7 | 20:56451792 | GGAAAGCTACTAACC[C/T]GGCAACTATGTGTGG | 57091 |
rs749650806 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445059 | AGTTTGCAGTGAGCC[A/G]AGATCGCGCCATTGC | 57091 |
rs749708959 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431694 | CTTTTACAATAGGCA[A/C]ATCCGCCAGCTAAGC | 57091 |
rs749724924 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419071 | GAGAATAGACAGGCA[-/C]TTGGCCGACACGATA | 57091 |
rs749857293 | snp | A/G | 1.64909e-05 | 0.00287144 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452592 | ATTCCGAGACTATCT[A/G]GAGGCCAACATTGAT | 57091 |
rs749870318 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | CASS4 | GRCh38.p7 | 20:56458465 | CGCATTTCACGGCAG[C/G]CTCAGCAGCAGCCAG | 57091 |
rs749877653 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414574 | ACACCACCGAGCCCC[A/G]CTGCAATTTGTAAAT | 57091 |
rs749927879 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428567 | AGCATGCCACAGCCT[C/G]CACCACACCCAAATG | 57091 |
rs749935160 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426651 | CACAATCCCGGCTCA[C/T]TGCAATCTCCACCTA | 57091 |
rs749967136 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440392 | ACAAAAAATCAATAG[C/T]AATTCCTTCCTCTCC | 57091 |
rs750092776 | snp | A/G | 1.7093e-05 | 0.00292339 | intron-variant | CASS4 | GRCh38.p7 | 20:56450584 | AAGTTGTCTGCCTTT[A/G]TGGTCTTTCCCCAGG | 57091 |
rs750106961 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459707 | ACTCCTGACCTCAGG[C/T]CATCCCCCGCCTCGG | 57091 |
rs750154860 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415744 | CCCTGAAGTTCGCCT[G/T]TGTACATCGTATGGT | 57091 |
rs750165813 | snp | C/T | 1.70522e-05 | 0.0029199 | intron-variant | CASS4 | GRCh38.p7 | 20:56458329 | TCTATTTTCTTCCTT[C/T]CCTTCTTTAGAATCC | 57091 |
rs750215005 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56453211 | GATGCTGAGACTCTT[C/T]CCATAGTGTATAGGC | 57091 |
rs750221595 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420322 | TAGGGTCATCCCTGT[A/G]TCTTGGAGGTGTTTG | 57091 |
rs750264568 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419134 | AGGGCCGTTTTGGAA[A/T]TGCGATGACTAAGGG | 57091 |
rs750268220 | snp | A/G | | | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56451836 | GCAGGGTGTTCCCCT[A/G]ATATCAGTGACTACC | 57091 |
rs750306849 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439510 | ACCTCATCTTTACTA[A/C]TAATAATAAAAAATA | 57091 |
rs750395450 | snp | A/G | 5.70153e-05 | 0.00533895 | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412415 | GCCTCTGAAGCTGGA[A/G]ATACTAGCTGCAGAG | 57091 |
rs750400828 | snp | A/G | 3.29506e-05 | 0.00405884 | missense | CASS4 | GRCh38.p7 | 20:56458430 | CGGCTCTACTTTGGG[A/G]CGCTCTTCAAAGCCA | 57091 |
rs750457693 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445615 | GACTCCGTCCAACTC[A/G]CGTGGGCCCAAGAAT | 57091 |
rs750518258 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431456 | ACAGTGTTTCATTCA[C/T]ATTGAGGGGAATCGT | 57091 |
rs750556352 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444809 | AACTGGCCAGGTGCT[C/G]TCAATAAAATATAAA | 57091 |
rs750605783 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418354 | GAGTAAACCAAGAGA[C/G]AGAGGGGTCAGAAGT | 57091 |
rs750619769 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427071 | GAGGCTGAGGCAGGA[A/G]GATTGCTTAAGACCA | 57091 |
rs750712364 | snp | A/G | 1.64966e-05 | 0.00287194 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452988 | GTTGACCCCAAATGC[A/G]GAATTTAAGTGTGAA | 57091 |
rs750731993 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424459 | TTAAGATACAGCTTC[A/G]GCCAGGCATGGTGGC | 57091 |
rs750778449 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442563 | CCACCCCAGAAGCCT[A/C]CAGTGCCTTCTCTCT | 57091 |
rs750785424 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436847 | AGCCAAGATTTCACC[A/G]CTGCACTCCAGCCTG | 57091 |
rs750874722 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425462 | CTCCATGCTGTACAC[A/G]GTCCAGGCCCTTTGA | 57091 |
rs750883793 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417428 | GGCCTCTCTGGACCA[C/T]GCTGTGCAAATCACT | 57091 |
rs750897129 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456905 | TGCCAAGGCTAGTCT[C/G]AAACTCCTAGGGTTA | 57091 |
rs750995912 | snp | C/T | 1.65765e-05 | 0.00287888 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56450634 | ATATGACATACCAGC[C/T]AGCCCCAAGAAGGCA | 57091 |
rs751067893 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56437960 | GGGGTTTCCATGGGT[C/T]CAGAGGCAAGAAGTT | 57091 |
rs751130042 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409685 | TTGCCAAGAGCATTA[A/G]GATTACCTCACTAGA | 57091 |
rs751161382 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426575 | TCTTCTTCTTCTTTC[C/T]GCCTCCCCCTCCCCC | 57091 |
rs751183692 | snp | A/G | 1.65045e-05 | 0.00287263 | missense | CASS4 | GRCh38.p7 | 20:56458386 | GTCAACAGACTCCTG[A/G]GAGGAAACCCCGCTT | 57091 |
rs751266001 | snp | C/G | 1.64754e-05 | 0.00287009 | missense | CASS4 | GRCh38.p7 | 20:56458524 | TGGTCATCATGGTGG[C/G]ACAGAAGCTGGTGGA | 57091 |
rs751275823 | snp | A/G | 1.76846e-05 | 0.00297354 | intron-variant | CASS4 | GRCh38.p7 | 20:56451768 | AAACAACGCACTCGC[A/G]CCCTCTTTGGAAAGC | 57091 |
rs751281257 | in-del | -/TTC | | | downstream-variant-500B, cds-indel | CASS4 | GRCh38.p7 | 20:56459445 | ATAGGGCTAGCTTGG[-/TTC]TTCTTCAATGTCTCC | 57091 |
rs751309869 | snp | C/G | 1.66502e-05 | 0.00288527 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452286 | GCTGGAGAAAGCCAA[C/G]GAGGTGTCAGAGAAT | 57091 |
rs751312557 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440989 | ACTTAAAAAAAAAAA[-/T]TTTTTTTTTTTTTTT | 57091 |
rs751343522 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418085 | GGTTCAGGGTGATCA[A/G]GACAGAGCTGACATT | 57091 |
rs751368675 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447797 | TGACAAACACACAAG[C/G]TCCCTTTGCCATGAT | 57091 |
rs751413761 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450303 | TGTTGGGATTACAGG[C/T]GTGAGCCACCACGCC | 57091 |
rs751436109 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431097 | AAAGAATGGATGTGA[A/G]GAACCAATTAGAATT | 57091 |
rs751489816 | snp | A/C | 3.84283e-05 | 0.00438323 | intron-variant | CASS4 | GRCh38.p7 | 20:56437610 | ACTTCCACCTACTAG[A/C]CATGGGTTGAGGGGT | 57091 |
rs751489871 | snp | A/G | 3.35272e-05 | 0.0040942 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452463 | TTCCTCGGAGGAGTC[A/G]GCAAAGGAGCTCTCC | 57091 |
rs751515479 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419077 | TAGACAGGCATTGGC[C/T]GACACGATAATGGAA | 57091 |
rs751606769 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412099 | CGAAGTAGGAACTTC[A/G]CCCTATAAAGCAGAA | 57091 |
rs751609355 | snp | A/G | 6.65657e-05 | 0.00576875 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453079 | AAGCAAAGGGAAGAT[A/G]AACACTCTTCTGAAC | 57091 |
rs751773397 | snp | A/T | 0.000161512 | 0.00898498 | intron-variant | CASS4 | GRCh38.p7 | 20:56453205 | TACTAAGATGCTGAG[A/T]CTCTTTCCATAGTGT | 57091 |
rs751776243 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444537 | CTCTAGAAAAATGTG[C/T]GCATTCCTAGTCCCC | 57091 |
rs751791193 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56412629 | TTGGAGATGGGAAAG[A/T]TTAACATAAGTTTAA | 57091 |
rs751993421 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56422154 | AAACCAAATATCTTA[A/G]GCAATAACTCAGGGA | 57091 |
rs751999781 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434183 | AACGTGACAGCATCC[A/G]GAGCCCTGATGGTTT | 57091 |
rs752067076 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444217 | CCCAGTGCTGCATCC[C/T]GGGGACACCATGATG | 57091 |
rs752109065 | snp | A/G | 5.68888e-05 | 0.00533302 | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412436 | AGCTGCAGAGCTCAG[A/G]GGAGCTGCTCCACAT | 57091 |
rs752129567 | snp | G/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411472 | GAATCACTTGAACCC[G/T]GGAGGTGGAGGTTGC | 57091 |
rs752134700 | snp | A/T | 1.64781e-05 | 0.00287033 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451906 | AAATCGGAATGGATT[A/T]ATGACACTCCAGTGT | 57091 |
rs752135387 | snp | A/G | 1.73863e-05 | 0.00294836 | intron-variant, synonymous-codon | CASS4 | GRCh38.p7 | 20:56437478 | TTATGAGCAGATGAG[A/G]AGTTGGGCGGAGGGG | 57091 |
rs752230636 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417832 | GCTGCCACTCAGCCT[C/G]TTCTCTTGACAATTG | 57091 |
rs752395583 | snp | C/T | 1.67545e-05 | 0.0028943 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452480 | CAAAGGAGCTCTCCT[C/T]GGACCTGGATGTGGC | 57091 |
rs752416290 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant | CASS4 | GRCh38.p7 | 20:56412523 | GGCTGTTTGAATGGG[C/T]TCTGGCGGGGAGCAA | 57091 |
rs752468509 | snp | A/G | 1.64776e-05 | 0.00287028 | missense | CASS4 | GRCh38.p7 | 20:56458538 | GGACAGAAGCTGGTG[A/G]ACACGCTGTGCATGG | 57091 |
rs752505811 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56430974 | CTTTTGTTCTGAATG[C/T]AGTTCTAAGCAATTA | 57091 |
rs752520853 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429541 | TTAGGAGCCAGGGCC[C/T]TTGTTGATCTCTCTC | 57091 |
rs752549459 | snp | C/G | 1.66718e-05 | 0.00288715 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452391 | TTCCAGTTCTGACAG[C/G]AGAGCTAGCATCGTT | 57091 |
rs752558298 | snp | C/T | 1.6607e-05 | 0.00288153 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458613 | AGTCACCTCTGCAGC[C/T]TGCTCAAGGACGTAG | 57091 |
rs752598850 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432175 | TTAGAGTGTGATTGC[-/A]AGGCTAAGTATGAAA | 57091 |
rs752644712 | in-del | -/TCT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429248 | CGGGCCAGTTCCCTC[-/TCT]TCTTCTTACTTTCCC | 57091 |
rs752746051 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444826 | CAATAAAATATAAAT[A/C]GGGGCCAGGCGCGGT | 57091 |
rs752780274 | snp | C/T | 1.65176e-05 | 0.00287376 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452180 | AGGTTCCTTCAAGCT[C/T]TCTGATTCCCCGAGT | 57091 |
rs752801323 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435185 | ACCTGCTTGTCTGGT[A/T]AAGATGGTATTTTTC | 57091 |
rs752835843 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420735 | ACGGTTGAAAGGGGA[A/G]TAGAAGCACAAGAGT | 57091 |
rs752871737 | in-del | -/C | 4.94319e-05 | 0.00497127 | frameshift-variant | CASS4 | GRCh38.p7 | 20:56458548 | GGTGGACACGCTGTG[-/C]CATGGAGACCCAGGA | 57091 |
rs752918046 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455679 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 57091 |
rs752926671 | snp | C/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410500 | ATCCCAGCACTTTGG[C/G]AGGCTAAGGCAGGTG | 57091 |
rs753016401 | snp | G/T | 1.67747e-05 | 0.00289605 | splice-donor-variant, missense | CASS4 | GRCh38.p7 | 20:56437426 | AGGAGACCTATCAGG[G/T]GCCCACTCTACCCCG | 57091 |
rs753132946 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443105 | TTCTGGGAGGTACCA[-/C]TGGCGGTACAGCCAG | 57091 |
rs753246501 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452860 | GATGACCTTGAGAGG[C/T]TTGTCATGGTGGCAC | 57091 |
rs753347040 | snp | C/G | 1.66966e-05 | 0.00288929 | missense | CASS4 | GRCh38.p7 | 20:56458635 | AGGACGTAGCGCTGG[C/G]CACTAAGAATGCCGT | 57091 |
rs753378214 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415865 | GCAGATTTTGTGTAA[C/T]ATCCAGACTGATTTA | 57091 |
rs753397576 | snp | C/T | | | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452042 | GTGGCAGATCCAGGT[C/T]CCTCACTCCACAACT | 57091 |
rs753507599 | snp | C/T | 1.67438e-05 | 0.00289338 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56445989 | CCAGCACCGGGGCCC[C/T]GTGGTCCTGAAGGTG | 57091 |
rs753526844 | snp | A/G | 3.29984e-05 | 0.00406179 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452582 | GGAAGTGGAGATTCC[A/G]AGACTATCTGGAGGC | 57091 |
rs753583968 | snp | A/G | 3.3521e-05 | 0.00409382 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452488 | CTCTCCTTGGACCTG[A/G]ATGTGGCCAAGGAGA | 57091 |
rs753716977 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428636 | CCCAGCTCCTATAAT[C/T]CTTTGAGTTTGCTGC | 57091 |
rs753765500 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56430135 | CCCAGATTTCTCCAA[A/G]TGCAGCTAAGACCAC | 57091 |
rs753845628 | snp | C/T | 1.66663e-05 | 0.00288667 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452343 | CTCCAGACGGACAAC[C/T]TCCCCATCTCCTGAA | 57091 |
rs753848476 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433864 | CCCTAACTCCTTTGG[A/G]GACCTTTTTTCTATG | 57091 |
rs753885243 | snp | A/G | 1.74983e-05 | 0.00295784 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437488 | ATGAGGAGTTGGGCG[A/G]AGGGGCCCCAGCCCC | 57091 |
rs753941603 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419247 | GATTAGAACACTCCA[A/T]CTTGAGTTGCAAAAA | 57091 |
rs753958554 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56446870 | GTTCCAGTCTAAATA[A/T]AATTTCAAGCAGGCT | 57091 |
rs753961555 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56453521 | GTGTTTCTTAGCAAC[A/G]AAAGAGGAAGTAGAA | 57091 |
rs754001763 | in-del | -/TTT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426545 | CTCTTCTTCTTCTTC[-/TTT]TTTTTTTTCCCCCTT | 57091 |
rs754025388 | snp | A/G | 1.91529e-05 | 0.00309452 | intron-variant | CASS4 | GRCh38.p7 | 20:56437593 | CCAAAACAGGTACGC[A/G]TACTTCCACCTACTA | 57091 |
rs754122631 | in-del | -/TTAA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415924 | CAAGGCGAAATTTTT[-/TTAA]TTAAAACACGTGATA | 57091 |
rs754133790 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413272 | TTGTGTTTTCATCTT[A/G]CTATGCCCTTTTTAA | 57091 |
rs754186572 | snp | A/G | 3.29614e-05 | 0.00405951 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452962 | AACTGTGAAAAGGAA[A/G]AGACTGTGCAGTTGA | 57091 |
rs754253327 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456979 | GTGTGGGTCACTGCA[A/C]TCAACCTGCTTCATT | 57091 |
rs754283564 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425552 | GAAGTCTTCCTGCAT[A/G]TGGCAAACTGCTTTT | 57091 |
rs754292396 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445685 | GCAGGTAAAGAACAT[C/T]GTGGGCCACGTGCGA | 57091 |
rs754293038 | snp | A/G | 4.94246e-05 | 0.0049709 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452002 | GCTCTCCCCAGTTCC[A/G]GCTCCACTTTCTACA | 57091 |
rs754337093 | snp | C/T | 1.85817e-05 | 0.00304803 | intron-variant | CASS4 | GRCh38.p7 | 20:56437116 | TGGAGTAGCAGTCAC[C/T]GGCCACGGTGCTAAC | 57091 |
rs754345307 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56458288 | GGAAAGGGCAGACAG[C/T]CACAGCCCATTGATT | 57091 |
rs754417275 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451928 | CTCCAGTGTCTCCAG[A/G]AAAGGCCAGCGTCAG | 57091 |
rs754541747 | snp | A/C | 1.65743e-05 | 0.00287869 | missense | CASS4 | GRCh38.p7 | 20:56450637 | TGACATACCAGCCAG[A/C]CCCAAGAAGGCAGGA | 57091 |
rs754634575 | snp | A/C | 1.89856e-05 | 0.00308098 | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412431 | ATACTAGCTGCAGAG[A/C]TCAGGGGAGCTGCTC | 57091 |
rs754635664 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56458049 | AAAGTTATAAATATA[A/G]TCATTGCCAATGTGT | 57091 |
rs754701454 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427073 | GGCTGAGGCAGGAGG[A/G]TTGCTTAAGACCAGG | 57091 |
rs754702385 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435674 | GAGAATTAGGAGACT[C/G]GGTTTGATCCTGGCT | 57091 |
rs754706687 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450332 | CCCGGCTGAGAAGTC[C/T]CTTTTTAAAGCACAA | 57091 |
rs754753293 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427114 | TGTAGTGCACCATGA[A/T]CATGCCTGTGAATAG | 57091 |
rs754781588 | snp | A/G | 1.66502e-05 | 0.00288527 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452289 | GGAGAAAGCCAAGGA[A/G]GTGTCAGAGAATTCC | 57091 |
rs754801286 | snp | C/T | 1.66654e-05 | 0.00288659 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452360 | CCCCATCTCCTGAAC[C/T]GGACAGATTATCAGG | 57091 |
rs754986601 | in-del | -/TG | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442830 | TAAACCTTTCGAAAC[-/TG]TGTTTCTCAAACATG | 57091 |
rs755066831 | snp | A/T | 0.000116621 | 0.00763524 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453081 | GCAAAGGGAAGATGA[A/T]CACTCTTCTGAACTA | 57091 |
rs755092294 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412130 | GAGTGGTGTTTTTTT[-/C]TTCTTCTTCTTCTTT | 57091 |
rs755108796 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418067 | TAGTTATTGGGCTCC[A/G]GGGGTTCAGGGTGAT | 57091 |
rs755138584 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454537 | TGAGAAAAGGAATCA[C/G]TAGGCAGAACCATCA | 57091 |
rs755149696 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433953 | AAGTTATTCCCTCAG[C/T]GGCATGAGGGCTGCA | 57091 |
rs755196040 | snp | A/C | 1.66551e-05 | 0.00288571 | missense | CASS4 | GRCh38.p7 | 20:56437321 | AAGGCCTGGCCCCTG[A/C]CAACCGCCTCCAAAT | 57091 |
rs755196041 | snp | A/T | 3.30207e-05 | 0.00406316 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452168 | ATGTCAGCTACAAGG[A/T]TCCTTCAAGCTTTCT | 57091 |
rs755206998 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439753 | AAGTAAGGAAGGAGA[A/G]AAAGAATGCGCTATT | 57091 |
rs755257229 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456077 | TTCTGGTCCAAGGAC[C/T]TCACTTGGAAAGCCC | 57091 |
rs755275115 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445066 | AGTGAGCCGAGATCG[C/T]GCCATTGCACTCCAG | 57091 |
rs755326072 | snp | A/T | 1.64819e-05 | 0.00287066 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452641 | GATCACATAGAAGAA[A/T]CTGTAAGAGAATTTC | 57091 |
rs755377297 | snp | A/G | 4.05605e-05 | 0.00450318 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458720 | GCTGGAGCAACACAC[A/G]CGGCAGTTCAGAGGG | 57091 |
rs755415780 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452756 | CCATCTCCAACTCCT[A/G]CCGCATCCTGCTTGA | 57091 |
rs755431672 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413275 | TGTTTTCATCTTGCT[A/G]TGCCCTTTTTAAATT | 57091 |
rs755597485 | snp | C/T | 4.24151e-05 | 0.00460497 | intron-variant | CASS4 | GRCh38.p7 | 20:56412529 | TTGAATGGGCTCTGG[C/T]GGGGAGCAAGCTGTG | 57091 |
rs755612104 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448417 | AGAACAGGCCATCCA[C/T]AGCACGGCTGCCACC | 57091 |
rs755629624 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459715 | CCTCAGGCCATCCCC[C/T]GCCTCGGCCTCCCAA | 57091 |
rs755654980 | snp | A/G | 1.89532e-05 | 0.00307835 | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412438 | CTGCAGAGCTCAGGG[A/G]AGCTGCTCCACATCA | 57091 |
rs755655823 | snp | A/G | 0.000100013 | 0.00707083 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452394 | CAGTTCTGACAGCAG[A/G]GCTAGCATCGTTTCC | 57091 |
rs755702620 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434212 | TTCCACCCACCGACT[A/T]CCCACTGAAGAATTT | 57091 |
rs755706125 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414678 | CAGATAGGCCGGGAG[C/T]GGTGGCTCATGCCTG | 57091 |
rs755726895 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415837 | AGTAGAGCTGCTTTC[A/G]CCTTTGTGCATGGCA | 57091 |
rs755757610 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447090 | GTTCACGCCTGTAGT[C/T]CCAGCTACTAGAGAG | 57091 |
rs755764439 | snp | G/T | 1.66225e-05 | 0.00288287 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458615 | TCACCTCTGCAGCCT[G/T]CTCAAGGACGTAGCG | 57091 |
rs755842923 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438020 | GCTGGGCATGGTGGC[C/T]TACACCTATCTATAT | 57091 |
rs755886334 | snp | A/G | 1.78611e-05 | 0.00298835 | intron-variant | CASS4 | GRCh38.p7 | 20:56445860 | TGTGATCATCAGAGT[A/G]ACATTTCCTTTTCCT | 57091 |
rs755962074 | snp | A/G | 6.70466e-05 | 0.00578954 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452482 | AAGGAGCTCTCCTTG[A/G]ACCTGGATGTGGCCA | 57091 |
rs756004451 | in-del | -/C | 1.77651e-05 | 0.00298031 | intron-variant, frameshift-variant | CASS4 | GRCh38.p7 | 20:56437499 | GCGGAGGGGCCCCAG[-/C]CCCCCTACTGCCCAA | 57091 |
rs756039782 | snp | A/C | 1.65157e-05 | 0.0028736 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453022 | TACATCCAGCCTCCC[A/C]AAAGAGAAACTGAAT | 57091 |
rs756049979 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426692 | AAGCCATCCTCCAGC[C/T]TCAGCCTCCCAAGTA | 57091 |
rs756069813 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439657 | CCTGCACTCCAGCCT[A/G]GGTGACTGACCGGGA | 57091 |
rs756117582 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | CASS4 | GRCh38.p7 | 20:56458484 | AGCAGCAGCCAGCCC[A/G]CGGAGATCATCACTC | 57091 |
rs756167828 | snp | C/T | 1.65244e-05 | 0.00287436 | stop-gained, intron-variant | CASS4 | GRCh38.p7 | 20:56452191 | AGCTTTCTGATTCCC[C/T]GAGTGGAACAGCAGA | 57091 |
rs756187603 | snp | A/G | 1.66026e-05 | 0.00288115 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452248 | CCTAAAGCAACGTCG[A/G]GTGTTTCTCAGGCTG | 57091 |
rs756191138 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427255 | CCAGAAATCCCTCCC[A/G]GAAGAAGTGTCTGTA | 57091 |
rs756216760 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431484 | CGTGTTATGGCAACA[C/T]ATTTAGAGTTTTCCT | 57091 |
rs756294045 | in-del | -/AAAAAAAAAA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413673 | GCAAGACTCTGTCTC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 57091 |
rs756307153 | in-del | -/GT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416530 | TCTGTTTACTTCCGT[-/GT]GTGTGTGTGTGTGTG | 57091 |
rs756369935 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436068 | CTTGTCATTCACTTA[A/T]TAATGAACATTTACT | 57091 |
rs756373478 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432891 | GGTCATCCAAAAGTG[C/T]GGGCAGGGGCGTCAC | 57091 |
rs756399168 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445098 | CTGGGCAACAGGAGC[A/G]AAGATCCATCTCAAA | 57091 |
rs756414497 | snp | C/T | 0.000209856 | 0.0102413 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437486 | AGATGAGGAGTTGGG[C/T]GGAGGGGCCCCAGCC | 57091 |
rs756417288 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455875 | AGCAGAGGTTGCGGT[A/G]AGCTGAGATCGCACC | 57091 |
rs756461708 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409831 | AGGCTCATTTGCCTT[A/G]AAATACTAATGGATT | 57091 |
rs756466731 | snp | C/T | 1.65817e-05 | 0.00287933 | missense | CASS4 | GRCh38.p7 | 20:56450659 | AAGGCAGGACTCCAT[C/T]CCCCAGACAGCCAAG | 57091 |
rs756554396 | snp | C/T | 1.76011e-05 | 0.00296652 | intron-variant | CASS4 | GRCh38.p7 | 20:56451786 | CTCTTTGGAAAGCTA[C/T]TAACCCGGCAACTAT | 57091 |
rs756557893 | snp | A/C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444848 | AGGCGCGGTGGCTCA[A/C/T]GCCTGTAATCCCAGC | 57091 |
rs756648607 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456923 | ACTCCTAGGGTTAAG[C/T]GATCCTCCTGCCTCG | 57091 |
rs756676506 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442757 | AAAGGGTCAGATTTC[C/T]TGGTGAAACTGCTTT | 57091 |
rs756760484 | snp | A/G | 1.67108e-05 | 0.00289052 | missense | CASS4 | GRCh38.p7 | 20:56437260 | ATTCTGGAGCAACAC[A/G]TGCCAGAAAGCGAGG | 57091 |
rs756812320 | snp | G/T | | | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459443 | TTATAGGGCTAGCTT[G/T]GTTCTTCTTCAATGT | 57091 |
rs756822677 | snp | A/G | 5.02534e-05 | 0.0050124 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452489 | TCTCCTTGGACCTGG[A/G]TGTGGCCAAGGAGAC | 57091 |
rs756876582 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426591 | GCCTCCCCCTCCCCC[A/G]CCAAGACAAGGTCTC | 57091 |
rs756910586 | snp | A/C | 3.3042e-05 | 0.00406447 | missense | CASS4 | GRCh38.p7 | 20:56445939 | GTCCGGGCCTCACTG[A/C]CGACTCTGCCTTCCC | 57091 |
rs756912515 | snp | A/C | 3.29886e-05 | 0.00406118 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452586 | GTGGAGATTCCGAGA[A/C]TATCTGGAGGCCAAC | 57091 |
rs756918541 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459535 | GGCGATTTTGTTTTA[A/T]TTTCTCGGTCAGGAA | 57091 |
rs756927168 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414472 | TTTTAGCAATGGGGG[C/T]ATCACTCTGTTGTCC | 57091 |
rs756980053 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413451 | GCCAAGGCAGGTGGA[G/T]CACTTGAGGCCAGGA | 57091 |
rs756996149 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56451174 | TGGTTGGGATAAGTC[A/G]TTTAACTTCTCTGTT | 57091 |
rs757116161 | snp | G/T | 3.43731e-05 | 0.00414552 | intron-variant | CASS4 | GRCh38.p7 | 20:56458319 | GAATCTCCTATCTAT[G/T]TTCTTCCTTCCCTTC | 57091 |
rs757147059 | snp | A/G | 0.0002346 | 0.010828 | missense | CASS4 | GRCh38.p7 | 20:56445990 | CAGCACCGGGGCCCC[A/G]TGGTCCTGAAGGTGA | 57091 |
rs757153716 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452049 | ATCCAGGTCCCTCAC[C/T]CCACAACTGAATAAC | 57091 |
rs757199048 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56437983 | AAGAAGTTACACATC[A/G]CATTTAAAATGTATA | 57091 |
rs757310195 | snp | A/C/T | 3.52636e-05 | 0.0041989 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437494 | AGTTGGGCGGAGGGG[A/C/T]CCCAGCCCCCTACTG | 57091 |
rs757342937 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442606 | CTAGGGTAACCACTA[C/T]CTTGAGCTTTGTTTT | 57091 |
rs757375015 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412127 | GAAGAGTGGTGTTTT[C/T]TTCTTCTTCTTCTTC | 57091 |
rs757429813 | snp | A/G | 3.29462e-05 | 0.00405857 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452876 | TTGTCATGGTGGCAC[A/G]GATGCTTCCAGAAGA | 57091 |
rs757466529 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417152 | TTCTGGGCAAGAAAG[C/T]CTGGTGAGGCTTCGT | 57091 |
rs757580413 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429832 | TCCCAACTGCACTTA[C/T]AATTTTTCATAACTT | 57091 |
rs757585031 | snp | C/T | 3.29674e-05 | 0.00405988 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452969 | AAAAGGAAGAGACTG[C/T]GCAGTTGACCCCAAA | 57091 |
rs757682272 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421098 | ACTCATTTCTCTGTC[A/G]TGCATTAAACAGCTT | 57091 |
rs757693391 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455834 | TACTCGGGAGGCTGA[G/T]GCAGGAGAATTGCTT | 57091 |
rs757710360 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435612 | CTGCCGTGGTAACAA[A/G]GCGACTTTTTTTAGA | 57091 |
rs757772296 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56422214 | GGCAGGCAGTGGCAA[C/G]GCTGTGAATGAACAC | 57091 |
rs757843808 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432981 | GATTTCTTACCTCTT[-/A]AAAGACTTGAAAATG | 57091 |
rs757945426 | snp | A/C | 1.6486e-05 | 0.00287102 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452601 | CTATCTGGAGGCCAA[A/C]ATTGATGCAATCCAC | 57091 |
rs757946572 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56446015 | AGGTGAGCCTTGTTC[A/G]GGGGCCCCTCATCAC | 57091 |
rs757957308 | snp | A/G | | | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412383 | AGCCAGAAGCATGCA[A/G]TGACATTGCACAATC | 57091 |
rs758070857 | snp | C/G | 1.6867e-05 | 0.002904 | intron-variant | CASS4 | GRCh38.p7 | 20:56450595 | CTTTGTGGTCTTTCC[C/G]CAGGAGCCAGAGAAG | 57091 |
rs758089658 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425659 | GACAAGCAGCTGCTT[A/G]AATTCACCAGCGCAG | 57091 |
rs758115367 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455695 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCG | 57091 |
rs758143554 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445533 | GCCTCCTGGTCCCTA[A/G]AGAACATCGGAATCA | 57091 |
rs758144686 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424834 | AGAGAAGACAGGAAT[A/G]AGCTGGCAAAAATGG | 57091 |
rs758190149 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429599 | TCCAACTTTCCATGC[A/G]CCCCCAACACATACA | 57091 |
rs758258870 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416021 | TCTAGCCAACTAGTC[A/T]ACTCCATTCAAGAAA | 57091 |
rs758270758 | snp | G/T | 0.000149553 | 0.00864604 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452260 | TCGAGTGTTTCTCAG[G/T]CTGGGAAGGAGCTGG | 57091 |
rs758286003 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416886 | GATGGTCCAATATTT[A/G]TACTGTAAGAACATT | 57091 |
rs758319604 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417836 | CCACTCAGCCTGTTC[G/T]CTTGACAATTGTCCC | 57091 |
rs758339672 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450424 | CTCAGACAAGGAAGG[C/T]GGGAGACCTGTCACC | 57091 |
rs758468679 | snp | C/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409615 | AGTGAATTGGTCAGA[C/T]TCACTTGTCTCAGAA | 57091 |
rs758494562 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454693 | GAGAAAGATAAACCT[A/G]TCTTGGAATAAAGGT | 57091 |
rs758545822 | snp | A/T | 1.64999e-05 | 0.00287222 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452996 | CAAATGCAGAATTTA[A/T]GTGTGAAAAATACAT | 57091 |
rs758647688 | snp | C/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410595 | TACAAAAAAATTAGC[C/T]GGGCATGGTGGCACG | 57091 |
rs758669315 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442436 | TGATCTTCTTTCACC[C/T]GACTCTGTGGCTGAC | 57091 |
rs758722397 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440784 | GCCTTGCTTGTGCAG[G/T]CTGTGGCAAACAACA | 57091 |
rs758762274 | snp | G/T | 1.66941e-05 | 0.00288908 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452517 | GACAGTGATGGCTCT[G/T]CAGCACAAGGTGGTC | 57091 |
rs758817220 | snp | G/T | 1.85331e-05 | 0.00304404 | intron-variant | CASS4 | GRCh38.p7 | 20:56437141 | GCTAACTGCAAATTC[G/T]CTTCTCCCCTCTCCA | 57091 |
rs758859344 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452023 | ACTTTCTACAATCCT[C/T]CAAGTGGCAGATCCA | 57091 |
rs758872171 | snp | A/G/T | 7.81057e-05 | 0.00624881 | synonymous-codon, missense | CASS4 | GRCh38.p7 | 20:56458711 | GGCTGAGAAGCTGGA[A/G/T]CAACACACGCGGCAG | 57091 |
rs758875509 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421010 | ACAAAAGAGTGGCTC[A/C]TTGCTTTCCTGAAGC | 57091 |
rs759018577 | snp | A/C | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452934 | TGCCAATGGAAGGCT[A/C]CTTTTTAAGCGGAAC | 57091 |
rs759102172 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56430895 | TGACTGGAGGGAAAT[A/G]AATGAGGGTAGAGCT | 57091 |
rs759106984 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424740 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 57091 |
rs759239514 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56451459 | GGCTGGCATTTCGCC[A/G]TGTCAGGGGGATGCA | 57091 |
rs759253046 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451979 | TTGCGGAAGAATCAA[A/G]GCCCCACGCTCTCCC | 57091 |
rs759293290 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56451896 | AAATCCTCAGAAATC[A/G]GAATGGATTTATGAC | 57091 |
rs759303817 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455621 | GTATCACAATCACCT[A/G]TGATCTTTGTTAAAA | 57091 |
rs759334702 | snp | A/G | 1.67778e-05 | 0.00289631 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452472 | GGAGTCAGCAAAGGA[A/G]CTCTCCTTGGACCTG | 57091 |
rs759357150 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444064 | TCATCCTGTTCGCAT[G/T]GCGGCTGCTTTGTCT | 57091 |
rs759381098 | snp | A/G | 0.000119508 | 0.00772914 | intron-variant | CASS4 | GRCh38.p7 | 20:56412509 | GGTGAGTGATGTGGG[A/G]CTGTTTGAATGGGCT | 57091 |
rs759420255 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56423540 | TTAAACATTACTTTA[C/T]TTTATTTATTTATTT | 57091 |
rs759456198 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410194 | AGTCTTTTCTAAGAG[A/G]CTTGAATTCAGTTTC | 57091 |
rs759538808 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442182 | TAAGAGTGGCCCCAA[A/C]TTAACATCCGAGAAG | 57091 |
rs759598500 | in-del | -/C | 3.41413e-05 | 0.00413153 | intron-variant | CASS4 | GRCh38.p7 | 20:56458329 | TCTATTTTCTTCCTT[-/C]CCTTCTTTAGAATCC | 57091 |
rs759637679 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444366 | GCAACAGCTCCTTGG[A/G]ACGCCAGTGGGAAGT | 57091 |
rs759641202 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421924 | TCCCTCAGATGGCTT[A/T]CATGAACTAAGAGGT | 57091 |
rs759659449 | snp | A/C | 0.000164596 | 0.00907032 | intron-variant | CASS4 | GRCh38.p7 | 20:56453206 | ACTAAGATGCTGAGA[A/C]TCTTTCCATAGTGTA | 57091 |
rs759688449 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435102 | TGTCTTTCTGGGTGC[A/G]TGAAGGATCTGATTC | 57091 |
rs759878557 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440153 | CCAGCACAGGCACTC[C/G]CTACAAACACCAGGA | 57091 |
rs759955848 | snp | C/T | 1.66674e-05 | 0.00288676 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452331 | TTCCTCATGGTTCTC[C/T]AGACGGACAACTTCC | 57091 |
rs759957814 | snp | A/G | 1.73875e-05 | 0.00294847 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437480 | ATGAGCAGATGAGGA[A/G]TTGGGCGGAGGGGCC | 57091 |
rs760013976 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56446934 | CACTTTTGGCCAGGT[A/G]CGGCAGCTCACACCT | 57091 |
rs760033219 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426502 | GTGAGGGGCTACATT[A/G]AATCTAAAAGATTAA | 57091 |
rs760063106 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459393 | CTGTGACCTTCAGAC[A/G]GCATAAATATGTGTG | 57091 |
rs760068087 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415565 | TATTAGTGCAGTTGA[G/T]CCATCTCATTAATCT | 57091 |
rs760079413 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56446494 | CTTAACACGGATTAT[C/T]ACTGATTATCTTAAC | 57091 |
rs760129283 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428038 | CCACCACTAGTTTGG[G/T]GAACTTCCTTATTTA | 57091 |
rs760186825 | snp | C/T | 1.85534e-05 | 0.00304571 | intron-variant, synonymous-codon | CASS4 | GRCh38.p7 | 20:56437544 | CGACCCTCCCACCAG[C/T]GCCAGAATCATCTGT | 57091 |
rs760335491 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416393 | TGTCTAAAAGACAAG[G/T]AGGATAAGTGGGCTT | 57091 |
rs760440082 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448141 | AGTGAGACTCTGTCT[-/C]AAAAAAAAAAAAAAA | 57091 |
rs760473733 | snp | G/T | 3.33356e-05 | 0.00408248 | missense | CASS4 | GRCh38.p7 | 20:56437346 | CCAAATCCTCACGGA[G/T]GTCGCTGCAGACAGG | 57091 |
rs760501860 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455481 | CTAGGACAAGAATTC[A/G]GGCCTCCTGATGCTC | 57091 |
rs760538278 | in-del | -/TT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454984 | AGGGGCTCTGCAAGG[-/TT]GTTGTGGGTGGTACT | 57091 |
rs760566656 | snp | C/G | 3.58012e-05 | 0.00423076 | missense | CASS4 | GRCh38.p7 | 20:56458676 | CCCAGCCCTGCCGCG[C/G]TGGGGCACCTCCAGG | 57091 |
rs760574497 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434885 | AGATCTGGAAACACA[A/G]AAACCGAAGGATTAA | 57091 |
rs760576215 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440414 | TTCCTCTCCCTGAAA[A/G]GAAAACAGATGCGCT | 57091 |
rs760669381 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415237 | TTATGCAGTCCTTAA[A/G]ATATGTACAGTCATT | 57091 |
rs760673902 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435151 | AGACTTGTAGTAGTG[-/T]TTCCCCTAATCCACA | 57091 |
rs760678234 | snp | C/T | | | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458870 | GAAACAGACCTGGTG[C/T]CCAAAGCTGGTAGTA | 57091 |
rs760697209 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56449670 | AATAAATAAATAATA[A/T]AATAAAATAAAATAA | 57091 |
rs760714763 | snp | C/G | 1.64754e-05 | 0.00287009 | missense | CASS4 | GRCh38.p7 | 20:56458492 | CCAGCCCGCGGAGAT[C/G]ATCACTCAGAGCAAG | 57091 |
rs760752577 | snp | A/G | 3.29533e-05 | 0.00405901 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452717 | ACAGTAACCTTCAGA[A/G]CAGAATTCGGGACCA | 57091 |
rs760772449 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56423788 | GACCTCAAGTGATCC[A/G]CACACCTCGGCGTCC | 57091 |
rs760776886 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433842 | ATGCCCCTCACAATA[C/T]ACATGCCCCTAACTC | 57091 |
rs760877875 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445616 | ACTCCGTCCAACTCG[C/T]GTGGGCCCAAGAATC | 57091 |
rs760902427 | snp | C/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410609 | CCGGGCATGGTGGCA[C/T]GCACCTATAATCCCA | 57091 |
rs760948691 | snp | C/G | 1.90033e-05 | 0.00308241 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437573 | GTGAAAAGACTCTCA[C/G]CTTTCCAAAACAGGT | 57091 |
rs761101859 | snp | A/G | 1.67298e-05 | 0.00289217 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452434 | ACCACATCCACCGAC[A/G]ACTCCTCCAGCTCTT | 57091 |
rs761152202 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56458137 | TGTATGTATTACAAT[A/G]TAATATTGTATATAT | 57091 |
rs761183534 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452946 | GCTCCTTTTTAAGCG[A/G]AACTGTGAAAAGGAA | 57091 |
rs761184541 | snp | C/T | | | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452742 | GGACCAGATGCAGAC[C/T]ATCTCCAACTCCTAC | 57091 |
rs761202174 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426274 | ACTCATCTCCTAAAT[C/G]AGATGTTAGTTATAG | 57091 |
rs761215875 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426378 | GAGTTGAGAACCCGC[A/G]AGCTATCCTGATTCC | 57091 |
rs761263769 | snp | C/G | 1.64961e-05 | 0.00287189 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452104 | AGCCTTCCAGAAATT[C/G]CTTCTTATGGCTTTC | 57091 |
rs761276707 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438731 | GCATGGTGGCAGGCA[C/T]CTGTAATTCCAGCTA | 57091 |
rs761295290 | snp | A/G | 1.66827e-05 | 0.00288809 | missense | CASS4 | GRCh38.p7 | 20:56437356 | ACGGAGGTCGCTGCA[A/G]ACAGGCCGTGCCCCC | 57091 |
rs761298980 | in-del | -/G | 0.000167117 | 0.00913951 | intron-variant | CASS4 | GRCh38.p7 | 20:56453172 | AAAGGGGCTTCAATT[-/G]TTACCTGGAGTAGTG | 57091 |
rs761379446 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454296 | CTTAAGAGGCCCAGA[A/C]GTCACTTGGGGGCTG | 57091 |
rs761401764 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419528 | AGCCTCCTGGCTTAA[C/G]TGATCCTCCCACCTC | 57091 |
rs761469998 | snp | C/T | 3.22888e-05 | 0.00401788 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458766 | CTGTCTACCTCCCTT[C/T]CTCCTCTGCTCACCT | 57091 |
rs761524521 | snp | A/G | 8.55293e-05 | 0.00653891 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437461 | CCCACTCCAGGCCCC[A/G]TTTATGAGCAGATGA | 57091 |
rs761605326 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420056 | TCTCAAAAACAAACA[A/G]ACAAAAGAAAGCTCC | 57091 |
rs761605770 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443934 | GGAAAGCTGGGCTTC[A/G]AGAGCCTAGGATTTC | 57091 |
rs761675318 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452795 | AAAGCTTGGATAATC[A/G]CAATTGGCCTCTGGA | 57091 |
rs761676974 | snp | G/T | 1.76742e-05 | 0.00297268 | intron-variant | CASS4 | GRCh38.p7 | 20:56450566 | ATTAGGAAAGAAACA[G/T]TCAAGTTGTCTGCCT | 57091 |
rs761759185 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432816 | TAATGATTCCGTGTG[C/G]AGACTAGTTACGCCT | 57091 |
rs761886641 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456755 | GAGATCATGGCTCAC[A/T]GCAGCCTCCACCACC | 57091 |
rs761910658 | snp | A/G | 1.66663e-05 | 0.00288667 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452349 | ACGGACAACTTCCCC[A/G]TCTCCTGAACCGGAC | 57091 |
rs761920912 | in-del | -/CT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433701 | TCGGCTGTAGCTCAG[-/CT]CTCTGCTTTTCAATG | 57091 |
rs761946319 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426134 | GAGTCTGTGCTAAGC[A/G]GAGTGGTTTGTAGGC | 57091 |
rs762003640 | snp | A/G | 1.6588e-05 | 0.00287988 | missense | CASS4 | GRCh38.p7 | 20:56445900 | TCCTTTCTCTCCAAG[A/G]CCATCCTCACGCTTC | 57091 |
rs762134511 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417573 | CCATGAGGGACAGAC[C/G]TGGGCTTTCTTACTC | 57091 |
rs762172786 | snp | A/G | 1.65927e-05 | 0.00288029 | missense | CASS4 | GRCh38.p7 | 20:56445972 | GTGTATGACGTGCCT[A/G]CCCAGCACCGGGGCC | 57091 |
rs762269026 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424413 | AATATTGATATGGAA[A/T]GCCACTGCAATTCAT | 57091 |
rs762283558 | snp | C/T | 3.35475e-05 | 0.00409544 | intron-variant | CASS4 | GRCh38.p7 | 20:56453153 | AGAGTTCCAAGTGAT[C/T]GAAAAAGGGGCTTCA | 57091 |
rs762343914 | snp | C/G | 1.92387e-05 | 0.00310145 | intron-variant | CASS4 | GRCh38.p7 | 20:56437624 | GACATGGGTTGAGGG[C/G]TATGGAAACACCCAG | 57091 |
rs762367653 | snp | A/G | 3.29527e-05 | 0.00405898 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452729 | AGAACAGAATTCGGG[A/G]CCAGATGCAGACCAT | 57091 |
rs762438061 | snp | A/G | 8.23784e-05 | 0.00641735 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452018 | GCTCCACTTTCTACA[A/G]TCCTCCAAGTGGCAG | 57091 |
rs762500030 | snp | C/T | 3.74693e-05 | 0.00432819 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458770 | CTACCTCCCTTCCTC[C/T]TCTGCTCACCTCTCA | 57091 |
rs762517792 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419829 | AGGTGGATCATCTGA[C/G]GTCGGGAGTTCAATA | 57091 |
rs762611920 | snp | G/T | 1.64735e-05 | 0.00286993 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452818 | CCTCTGGAAGTTCTT[G/T]TGACTGACAGTGTCC | 57091 |
rs762636981 | snp | C/T | 1.64942e-05 | 0.00287173 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451879 | GGTTACAGCACATTA[C/T]CAAATCCTCAGAAAT | 57091 |
rs762687571 | snp | A/C | | | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452841 | CAGTGTCCAGAACAG[A/C]CCAGATGACCTTGAG | 57091 |
rs762763686 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432615 | TCAAGTCATCCACAC[A/G]CTTTGGCCTCCCAAA | 57091 |
rs762812540 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56412928 | GCCTCCCGTGCTGAG[C/T]CCACAGTGGGCACTT | 57091 |
rs762817861 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458507 | CATCACTCAGAGCAA[A/G]CTGGTCATCATGGTG | 57091 |
rs762905640 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444418 | CCGGAGCTTCACCCT[A/G]TCCTCTCCTCCAGGC | 57091 |
rs762909780 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457504 | ATTTTGATGAAACCT[C/T]ATTAGCAAATATGAT | 57091 |
rs762957785 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431040 | TTTATGTGTATAAAA[C/T]AAAATATTCTGGCTA | 57091 |
rs763001141 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445453 | CCCTCTGCCTATTGC[A/G]TGCACTTCTCCAGCC | 57091 |
rs763040775 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428097 | ACTGTATGATTTACC[A/T]TCCCAAAGAAAGAAT | 57091 |
rs763082149 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436705 | AACCAGCCTGGGCAA[C/T]GGCAAAACCCCTTCT | 57091 |
rs763115231 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425197 | AGCAGGAAGGGCAGC[C/G]AGCCTCCCCCAGGAG | 57091 |
rs763170260 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56423635 | CTGCAACCTCCACCT[C/G]CCAAGTTCAAGCAAT | 57091 |
rs763243640 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456431 | CAGGTGGGAGTGCAG[C/T]GGCGTGATCTCAGCT | 57091 |
rs763260720 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56446065 | GTCTGGGGTTCTTGG[A/G]ATCATGCCCACATTG | 57091 |
rs763279030 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429149 | TGCAGGAGCTGCTTC[C/T]CTCCCGGCTCATCTA | 57091 |
rs763298768 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455701 | TTGGGAGGCCGAGGC[A/G]GGTGGATCGCCTGAG | 57091 |
rs763320444 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444145 | TGCTAATGTTTACCA[C/T]CCAAGCCGTACACAT | 57091 |
rs763382815 | snp | C/G | 1.65015e-05 | 0.00287237 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452133 | TCTTGTACCCAGAGG[C/G]ACATTTCCTTTGGAT | 57091 |
rs763382930 | snp | A/G | 3.30808e-05 | 0.00406686 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458369 | TATACCTCAGCCTTC[A/G]AGTCAACAGACTCCT | 57091 |
rs763403845 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416329 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 57091 |
rs763423641 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435238 | TTTTGTAACAGAATA[C/G]AGATATTAGGCAAGA | 57091 |
rs763434501 | snp | A/G | 0.000158625 | 0.00890435 | intron-variant | CASS4 | GRCh38.p7 | 20:56453169 | GAAAAAGGGGCTTCA[A/G]TTGTTACCTGGAGTA | 57091 |
rs763457063 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415739 | TCAGACCCTGAAGTT[C/T]GCCTTTGTACATCGT | 57091 |
rs763486298 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450241 | GTTGGCCAGGCTGGT[C/T]TCGAACTCCCGACCT | 57091 |
rs763578592 | snp | C/G/T | 3.34517e-05 | 0.00408961 | missense, synonymous-codon | CASS4 | GRCh38.p7 | 20:56437259 | CATTCTGGAGCAACA[C/G/T]GTGCCAGAAAGCGAG | 57091 |
rs763631609 | snp | C/T | 3.29511e-05 | 0.00405887 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451993 | AGGCCCCACGCTCTC[C/T]CCAGTTCCAGCTCCA | 57091 |
rs763751368 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431079 | AGAGTGGATTATAAG[A/G]TGAAAGAATGGATGT | 57091 |
rs763814613 | snp | C/T | 1.67593e-05 | 0.00289471 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452484 | GGAGCTCTCCTTGGA[C/T]CTGGATGTGGCCAAG | 57091 |
rs763830863 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440227 | TAACTCTCTTTTCTG[A/G]AACAACTGGCCCCGA | 57091 |
rs763867794 | snp | A/G | 1.66807e-05 | 0.00288792 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458630 | GCTCAAGGACGTAGC[A/G]CTGGCCACTAAGAAT | 57091 |
rs763873159 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426642 | GAGCAGTGGCACAAT[C/G]CCGGCTCATTGCAAT | 57091 |
rs763896927 | snp | C/G | 1.78928e-05 | 0.002991 | intron-variant | CASS4 | GRCh38.p7 | 20:56450548 | TGTTCGTGATGTGTA[C/G]CCATTAGGAAAGAAA | 57091 |
rs763974572 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417882 | TCAGATGTTGCCTTA[G/T]ATGCAAGCTGTTGCT | 57091 |
rs764045834 | snp | A/G | 1.65132e-05 | 0.00287339 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452568 | GCTCTTTGTCAGCAG[A/G]AAGTGGAGATTCCGA | 57091 |
rs764102215 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454982 | GTAGGGGCTCTGCAA[C/G]GTTGTTGTGGGTGGT | 57091 |
rs764105882 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424079 | CATCTCTCACTTAAC[C/T]ACTTTGCTAAGTTTT | 57091 |
rs764134356 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432728 | CTAGTCCCTTAAATA[C/T]TTCATCACTGCTGGA | 57091 |
rs764139797 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452722 | AACCTTCAGAACAGA[A/G]TTCGGGACCAGATGC | 57091 |
rs764146773 | snp | C/T | 3.32182e-05 | 0.00407529 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452255 | CAACGTCGAGTGTTT[C/T]TCAGGCTGGGAAGGA | 57091 |
rs764159788 | in-del | -/TCT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426532 | AAGAGGATTTTTCCC[-/TCT]TCTTCTTCTTCTTTT | 57091 |
rs764199798 | snp | C/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410627 | ACCTATAATCCCAGC[C/T]ACTTGGGAGGCTGAG | 57091 |
rs764225159 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458495 | GCCCGCGGAGATCAT[C/T]ACTCAGAGCAAGCTG | 57091 |
rs764232851 | snp | A/G | 0.000122396 | 0.00782195 | intron-variant, synonymous-codon | CASS4 | GRCh38.p7 | 20:56437487 | GATGAGGAGTTGGGC[A/G]GAGGGGCCCCAGCCC | 57091 |
rs764235898 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455728 | TGAGGTCAGGAGTTT[A/G]AGACCAGCCTGACCA | 57091 |
rs764276341 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56412861 | CACTCTAACTGTCCT[A/G]TTTGGTTTCTGTGCT | 57091 |
rs764334532 | snp | C/T | 1.91415e-05 | 0.0030936 | intron-variant | CASS4 | GRCh38.p7 | 20:56437590 | TTTCCAAAACAGGTA[C/T]GCATACTTCCACCTA | 57091 |
rs764387425 | snp | A/G | 1.66657e-05 | 0.00288662 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452340 | GTTCTCCAGACGGAC[A/G]ACTTCCCCATCTCCT | 57091 |
rs764405758 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411958 | CAGGAAGGAAGAAAT[A/G]CTGACCGCTATCAGA | 57091 |
rs764508542 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436746 | ACAAAATTTAGCCCG[A/G]GGTGGCGGCACGCAT | 57091 |
rs764510496 | snp | A/G | 3.29576e-05 | 0.00405928 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452955 | TAAGCGGAACTGTGA[A/G]AAGGAAGAGACTGTG | 57091 |
rs764535764 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451918 | ATTTATGACACTCCA[C/G]TGTCTCCAGGAAAGG | 57091 |
rs764557984 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450272 | CAGGTGATCCTCCTG[C/T]CTCAGCCTCCCCAAG | 57091 |
rs764576764 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56422143 | AACAGTTCCCCAAAC[C/G]AAATATCTTAAGCAA | 57091 |
rs764664098 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56446600 | GTAAGACATGCTTCA[-/T]GTGATCAAAAAATAG | 57091 |
rs764672144 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417807 | TAACCCCTACCTGGC[A/G]TCAGCCTAAGCTGCC | 57091 |
rs764846022 | snp | A/G | 3.33723e-05 | 0.00408473 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56437361 | GGTCGCTGCAGACAG[A/G]CCGTGCCCCCCATTC | 57091 |
rs764860072 | snp | C/T | 1.8711e-05 | 0.00305862 | missense | CASS4 | GRCh38.p7 | 20:56458698 | ACCTCCAGGCGGAGG[C/T]TGAGAAGCTGGAGCA | 57091 |
rs764870089 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411795 | ATGTTATTCATTAGG[C/T]ACCATGAGCAAAGAC | 57091 |
rs764900573 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442312 | ATTAGAACAACTCTT[A/C]ATTTTACAGATGAGG | 57091 |
rs764950952 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417370 | CCCCTGCTGTTCCCC[A/G]CCTTGGATTCTTCTC | 57091 |
rs764981924 | snp | C/T | 1.64906e-05 | 0.00287142 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452591 | GATTCCGAGACTATC[C/T]GGAGGCCAACATTGA | 57091 |
rs765078815 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432949 | GACAGAAATAGGAGC[A/G]CTCATCCTGGTGTTT | 57091 |
rs765133519 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458426 | CTGCCGGCTCTACTT[C/T]GGGGCGCTCTTCAAA | 57091 |
rs765133989 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429516 | CTATAAACAGCATCC[G/T]CTATGGAAATTAGGA | 57091 |
rs765158070 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416594 | GTAATATTGAAATTA[A/G]CATCTTCATACACAG | 57091 |
rs765185176 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420991 | CAAAAGAAGAAAAGC[G/T]TAAACAAAAGAGTGG | 57091 |
rs765235539 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56449403 | TCACAGGTGGGAAAT[A/G]AACAATGAGAACACT | 57091 |
rs765265371 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444096 | CATCCGTGAGTCTAG[C/T]CAGATGAATGGCGGG | 57091 |
rs765282389 | snp | G/T | 1.72982e-05 | 0.00294088 | intron-variant | CASS4 | GRCh38.p7 | 20:56450708 | GGTGCTAAGGTGCGG[G/T]GTTATGAACACACAA | 57091 |
rs765291806 | in-del | -/G | 1.64883e-05 | 0.00287122 | frameshift-variant | CASS4 | GRCh38.p7 | 20:56458460 | ATCAGCGCATTTCAC[-/G]GCAGCCTCAGCAGCA | 57091 |
rs765303062 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448239 | TAGACCCTGTCTTTA[G/T]GTAAAACTGTGACAT | 57091 |
rs765303181 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433954 | AGTTATTCCCTCAGC[A/G]GCATGAGGGCTGCAG | 57091 |
rs765312659 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429019 | AAGCAGAGAAGCAAG[A/C]TGTGCATGTGGGCGA | 57091 |
rs765369011 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56423627 | TCAGCTCACTGCAAC[C/T]TCCACCTCCCAAGTT | 57091 |
rs765370913 | snp | C/T | 1.92088e-05 | 0.00309904 | intron-variant | CASS4 | GRCh38.p7 | 20:56437607 | CATACTTCCACCTAC[C/T]AGACATGGGTTGAGG | 57091 |
rs765370966 | snp | C/G | 1.67705e-05 | 0.00289568 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452455 | TCCAGCTCTTCCTCG[C/G]AGGAGTCAGCAAAGG | 57091 |
rs765486346 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410468 | GCATTGGCCAGGTGC[A/G]GTGGCTCACACCTAT | 57091 |
rs765534010 | snp | A/G | 0.000379078 | 0.0137621 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452970 | AAAGGAAGAGACTGT[A/G]CAGTTGACCCCAAAT | 57091 |
rs765539512 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56422076 | ACTTGCCTCCTCCTT[A/C]GGTGGGTTTTTCATG | 57091 |
rs765604840 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459522 | CACTGGGGAGTGGGG[C/T]GATTTTGTTTTAATT | 57091 |
rs765618875 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56454547 | AATCAGTAGGCAGAA[A/C]CATCAACAGAAAATA | 57091 |
rs765635623 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414305 | AATCTAGAACAATCT[A/G]CTACCTTTTTCTCTT | 57091 |
rs765643457 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428250 | CAAGGAGGAAGCAGG[A/T]TGGGGCCATGATGCT | 57091 |
rs765647671 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442510 | ATGCTACGTTACAGC[C/T]CTGTAACTTATATCC | 57091 |
rs765680973 | in-del | -/GGAG | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443101 | TGTTTCTGGGAGGTA[-/GGAG]CCACTGGCGGTACAG | 57091 |
rs765728156 | snp | C/G | 1.64996e-05 | 0.0028722 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452119 | CCTTCTTATGGCTTT[C/G]TTGTACCCAGAGGCA | 57091 |
rs765762144 | snp | A/G | 0.000132809 | 0.0081478 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453070 | CCTTCCACTAAGCAA[A/G]GGGAAGATGAACACT | 57091 |
rs765826913 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429262 | CTCTTCTTCTTACTT[C/T]CCCTGGCCCATTCAG | 57091 |
rs765855244 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459505 | CAGTTTTCATCTGAA[C/T]CCACTGGGGAGTGGG | 57091 |
rs765872102 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415698 | AACAACCCTGCCTTT[C/T]ATTCAGGGCCACCGC | 57091 |
rs765902094 | snp | A/G | 3.55758e-05 | 0.00421742 | intron-variant | CASS4 | GRCh38.p7 | 20:56450723 | TGTTATGAACACACA[A/G]AATCCTCTCAGAAAT | 57091 |
rs765956674 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452822 | TGGAAGTTCTTGTGA[C/T]TGACAGTGTCCAGAA | 57091 |
rs765987665 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416416 | GTGGGCTTATTATAC[A/G]TAAGTTCTTATTTTG | 57091 |
rs766043484 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417584 | AGACCTGGGCTTTCT[C/T]ACTCAGTGCTGCATC | 57091 |
rs766064182 | snp | C/T | 3.32182e-05 | 0.00407529 | missense | CASS4 | GRCh38.p7 | 20:56450627 | AGCAGTTATATGACA[C/T]ACCAGCCAGCCCCAA | 57091 |
rs766244581 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447793 | TCCATGACAAACACA[A/C]AAGCTCCCTTTGCCA | 57091 |
rs766264727 | snp | A/G | 1.93691e-05 | 0.00311194 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56412488 | CATCATGGACTGTGC[A/G]CCCAAGGTGAGTGAT | 57091 |
rs766318673 | snp | A/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411143 | TTTAAAAATAAAAAA[A/T]TAAAAAATGCTGTCT | 57091 |
rs766353597 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440420 | TCCCTGAAAGGAAAA[C/T]AGATGCGCTGTCCTC | 57091 |
rs766373165 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458510 | CACTCAGAGCAAGCT[A/G]GTCATCATGGTGGGA | 57091 |
rs766393930 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455493 | TTCAGGCCTCCTGAT[G/T]CTCAGCTCCCTGAAC | 57091 |
rs766452308 | snp | A/C | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410094 | CTGTATTATGAGCTT[A/C]AGGGCAGGCTCTTCA | 57091 |
rs766457723 | snp | A/G | | | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458959 | GTCAGGTATGAGGTA[A/G]AGACCTTGTGAAGTT | 57091 |
rs766486548 | snp | A/G | 4.98583e-05 | 0.00499266 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56445977 | TGACGTGCCTACCCA[A/G]CACCGGGGCCCCGTG | 57091 |
rs766603900 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420030 | CCTGGGCAACAAGAG[C/T]GAAAACTCCATCTCA | 57091 |
rs766682009 | in-del | -/TT | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410787 | TACCTGAATTATATC[-/TT]AATATAATATTAATA | 57091 |
rs766686684 | snp | A/G | 0.000104674 | 0.00723366 | intron-variant | CASS4 | GRCh38.p7 | 20:56453191 | CCTGGAGTAGTGGCT[A/G]CTAAGATGCTGAGAC | 57091 |
rs766705059 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429609 | CATGCGCCCCCAACA[C/T]ATACATACACACTCA | 57091 |
rs766723589 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432765 | AAGCTCAGCACCCAC[A/G]TTCTTGTGAAACCCA | 57091 |
rs766739822 | snp | A/T | 1.66297e-05 | 0.0028835 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453077 | CTAAGCAAAGGGAAG[A/T]TGAACACTCTTCTGA | 57091 |
rs766798965 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425530 | TCCTGGAAGTTCAGG[A/G]AGGTAAGAAGTCTTC | 57091 |
rs766842414 | snp | C/T | 1.66654e-05 | 0.00288659 | utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56458792 | CACCTCTCAGCTTCA[C/T]ACCCACAACTTGTGC | 57091 |
rs766870250 | snp | A/G | 3.46141e-05 | 0.00416003 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437475 | CGTTTATGAGCAGAT[A/G]AGGAGTTGGGCGGAG | 57091 |
rs766918491 | snp | A/G | 3.30033e-05 | 0.00406209 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452134 | CTTGTACCCAGAGGC[A/G]CATTTCCTTTGGATG | 57091 |
rs766965284 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440342 | ACATTAACTGAAGTT[A/G]ACTTGAATTTCTTCC | 57091 |
rs767006633 | snp | A/G | 1.65864e-05 | 0.00287974 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452238 | TTATGACATCCCTAA[A/G]GCAACGTCGAGTGTT | 57091 |
rs767024116 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439499 | AACATAGTGAGACCT[C/T]ATCTTTACTAATAAT | 57091 |
rs767037963 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56412514 | GTGATGTGGGGCTGT[G/T]TGAATGGGCTCTGGC | 57091 |
rs767046526 | snp | G/T | 1.64776e-05 | 0.00287028 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458537 | GGGACAGAAGCTGGT[G/T]GACACGCTGTGCATG | 57091 |
rs767117829 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428438 | GCCCCCTGACTATTA[A/T]CGTTGAGTTTGCAAA | 57091 |
rs767140530 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459682 | ACCATATTAGCCAGG[C/T]TGGTCTGGAACTCCT | 57091 |
rs767171464 | snp | C/T | 3.29571e-05 | 0.00405924 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451904 | AGAAATCGGAATGGA[C/T]TTATGACACTCCAGT | 57091 |
rs767224405 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447002 | CACTTGACACTAGGA[A/G]TTCGAGACCAGCCCA | 57091 |
rs767310064 | snp | G/T | 1.65252e-05 | 0.00287443 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452564 | TGATGCTCTTTGTCA[G/T]CAGGAAGTGGAGATT | 57091 |
rs767393342 | snp | A/G | 5.33879e-05 | 0.00516634 | missense | CASS4 | GRCh38.p7 | 20:56437212 | CCTGACTGCTCTGAC[A/G]AGCTGGCTTTCAGCA | 57091 |
rs767396207 | snp | A/T | 1.65206e-05 | 0.00287403 | missense | CASS4 | GRCh38.p7 | 20:56445925 | CGCTTCCCAGACCTG[A/T]CCGGGCCTCACTGCC | 57091 |
rs767407539 | snp | C/T | 1.66018e-05 | 0.00288108 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458612 | CAGTCACCTCTGCAG[C/T]CTGCTCAAGGACGTA | 57091 |
rs767502492 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56453186 | TGTTACCTGGAGTAG[G/T]GGCTACTAAGATGCT | 57091 |
rs767593258 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420215 | GCTTCACCTTATCAT[C/G]AAGAGCAGCTTTTGT | 57091 |
rs767597890 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457803 | GCAGATCATTTGAGA[G/T]CAGGGGTTCAAAACC | 57091 |
rs767639107 | snp | A/C | 1.6517e-05 | 0.00287372 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452178 | CAAGGTTCCTTCAAG[A/C]TTTCTGATTCCCCGA | 57091 |
rs767687124 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444340 | AGCCAACTTGGAAAG[-/C]CCCCTACTGAGCAAC | 57091 |
rs767728589 | snp | C/T | 3.31961e-05 | 0.00407394 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452246 | TCCCTAAAGCAACGT[C/T]GAGTGTTTCTCAGGC | 57091 |
rs767829746 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445586 | CAGGTTCCCGGCCCC[C/T]CTCGACACCCAGAGA | 57091 |
rs767905395 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425386 | CCCTACTCTCAAGGA[A/G]GAGGTAAATGCTCAC | 57091 |
rs767950409 | snp | A/G | 5.77217e-05 | 0.00537192 | intron-variant | CASS4 | GRCh38.p7 | 20:56437630 | GGTTGAGGGGTATGG[A/G]AACACCCAGAGGCCT | 57091 |
rs767982926 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419867 | GACCAACATGGAGAA[A/G]CCCCATCTCTACTAA | 57091 |
rs767993594 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452850 | GAACAGCCCAGATGA[C/T]CTTGAGAGGTTTGTC | 57091 |
rs768002267 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450294 | CTCCCCAAGTGTTGG[A/G]ATTACAGGCGTGAGC | 57091 |
rs768034851 | snp | A/C/G | 0.000244134 | 0.0110458 | intron-variant, stop-gained, missense | CASS4 | GRCh38.p7 | 20:56437484 | GCAGATGAGGAGTTG[A/C/G]GCGGAGGGGCCCCAG | 57091 |
rs768091162 | snp | C/T | 2.02427e-05 | 0.00318134 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56453123 | TAGGGCAAATATCTG[C/T]GGACAGGTGAGTTCA | 57091 |
rs768189515 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455052 | ACATTCTGATTTAAT[C/G]TTTCTGATTACAACA | 57091 |
rs768196425 | snp | A/C/G | 8.24048e-05 | 0.00641844 | missense | CASS4 | GRCh38.p7 | 20:56458460 | ATCAGCGCATTTCAC[A/C/G]GCAGCCTCAGCAGCA | 57091 |
rs768197172 | snp | C/T | 1.66846e-05 | 0.00288826 | missense | CASS4 | GRCh38.p7 | 20:56458350 | TTTAGAATCCTGGCC[C/T]TCTTATACCTCAGCC | 57091 |
rs768201081 | in-del | -/G | 1.75562e-05 | 0.00296273 | intron-variant | CASS4 | GRCh38.p7 | 20:56446016 | GGTGAGCCTTGTTCA[-/G]GGGCCCCTCATCACC | 57091 |
rs768228596 | snp | C/G | 4.96315e-05 | 0.00498129 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452210 | TGGAACAGCAGAACA[C/G]CAAGCCCAATATTTA | 57091 |
rs768289804 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457211 | TCAGTTTTATGCCCT[A/T]TCTGTCTGAATGCTT | 57091 |
rs768376726 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421221 | TTTGTACAATACTGG[C/T]GTATCTTGATTTGCA | 57091 |
rs768553305 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414839 | GTATTCCCAGCTACT[C/G]GGGAGGCTGAGGCAG | 57091 |
rs768615846 | in-del | -/CAA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419245 | GAGATTAGAACACTC[-/CAA]CTTGAGTTGCAAAAA | 57091 |
rs768670405 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452793 | GGAAAGCTTGGATAA[C/T]CGCAATTGGCCTCTG | 57091 |
rs768702760 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447410 | CTGGTTCACCATCTC[A/G]GGTTTCTACCCTTTC | 57091 |
rs768716950 | snp | C/T | 1.67335e-05 | 0.00289248 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452442 | CACCGACGACTCCTC[C/T]AGCTCTTCCTCGGAG | 57091 |
rs768854425 | snp | A/G | 5.53695e-05 | 0.00526134 | intron-variant | CASS4 | GRCh38.p7 | 20:56437160 | CTCCCCTCTCCACCC[A/G]CAGGCACTCCTGGCC | 57091 |
rs768877331 | snp | A/G | 1.65015e-05 | 0.00287237 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458582 | GGACGTGCGCAACGA[A/G]ATCCTCCGTGGCAGC | 57091 |
rs768899601 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425206 | GGCAGCGAGCCTCCC[C/T]CAGGAGCTTTGAGAT | 57091 |
rs768909527 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451954 | GTCAGAAACACGCCT[C/G]TCACCAGCTTTGCGG | 57091 |
rs768942386 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431124 | AATTTAAGTGACCTT[G/T]GACAAGTCATTTGAT | 57091 |
rs768947672 | snp | C/T | 1.66799e-05 | 0.00288785 | intron-variant | CASS4 | GRCh38.p7 | 20:56445892 | TTTTCTCCTCCTTTC[C/T]CTCCAAGGCCATCCT | 57091 |
rs769115638 | in-del | -/AG | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418178 | GAAAGAGGAGAAAAC[-/AG]GGGGATCTGATGGAG | 57091 |
rs769264148 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56453282 | TATGAAAGTAAAATT[A/C]TTGATGAAATCTTAT | 57091 |
rs769333762 | snp | C/G/T | 0.000101171 | 0.0071117 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452306 | TGTCAGAGAATTCCG[C/G/T]GGGCCATAATTCCTC | 57091 |
rs769391598 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56422148 | TTCCCCAAACCAAAT[A/T]TCTTAAGCAATAACT | 57091 |
rs769423454 | snp | A/C | 1.82307e-05 | 0.00301911 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437526 | CCAAGTCTATGAATT[A/C]CCCGACCCTCCCACC | 57091 |
rs769472005 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418735 | AGCAGAAAAAATAGT[A/G]AATCAAGGAGTAGAT | 57091 |
rs769584033 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413565 | GTGATCCCAGCTACT[C/T]GGGAGGCTGAGGCAC | 57091 |
rs769612383 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445358 | CCTGCCTCAGCCCAG[C/G]TGACAAGTCCTTAGA | 57091 |
rs769645018 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425946 | TTTTAAAAAATTTAA[C/T]ACTACATTTTGGAGA | 57091 |
rs769672311 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456324 | GTTAATATTTTCACT[A/T]AAGATGCTCATAATC | 57091 |
rs769790444 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56412806 | CTGCCTCAGCCCCCG[C/T]TAATTCCTTCTTTCT | 57091 |
rs769816537 | snp | C/T | 1.65679e-05 | 0.00287814 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56451863 | TACCTTAAGAAGAGG[C/T]GGTTACAGCACATTA | 57091 |
rs769818061 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450124 | GCAACCTCCACCTCC[A/C]AGGTTCAAGAGATTC | 57091 |
rs769832762 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425340 | ATTTAACAGTCATTC[A/G]TTGCCCTCTCTGTGT | 57091 |
rs769925748 | snp | A/G | 2.21757e-05 | 0.00332977 | missense | CASS4 | GRCh38.p7 | 20:56458734 | CGCGGCAGTTCAGAG[A/G]GACACTGGGATGAGG | 57091 |
rs769945049 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56453762 | GGTGTAGTGGCTCAT[A/G]CACTTGGGAGTCTGA | 57091 |
rs769966727 | snp | A/C/G/T | 0.000232338 | 0.0107759 | missense | CASS4 | GRCh38.p7 | 20:56445973 | TGTATGACGTGCCTA[A/C/G/T]CCAGCACCGGGGCCC | 57091 |
rs769993078 | snp | C/T | 0.00011682 | 0.00764173 | missense | CASS4 | GRCh38.p7 | 20:56437363 | TCGCTGCAGACAGGC[C/T]GTGCCCCCCATTCCT | 57091 |
rs770021620 | snp | C/G/T | 3.30662e-05 | 0.00406598 | synonymous-codon, missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452559 | TGGCCTGATGCTCTT[C/G/T]GTCAGCAGGAAGTGG | 57091 |
rs770064559 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417440 | CCACGCTGTGCAAAT[C/T]ACTTCCCCCCTACAC | 57091 |
rs770317129 | snp | A/G | 6.59304e-05 | 0.00574116 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452644 | CACATAGAAGAATCT[A/G]TAAGAGAATTTCTGG | 57091 |
rs770375718 | snp | C/T | 1.66147e-05 | 0.0028822 | missense | CASS4 | GRCh38.p7 | 20:56458359 | CTGGCCCTCTTATAC[C/T]TCAGCCTTCGAGTCA | 57091 |
rs770378111 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443752 | GGCTGGACGAGGGCC[A/G]CTCTCCCCTTGGGAA | 57091 |
rs770422106 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457224 | CTATCTGTCTGAATG[C/G]TTCCGGGCTATGAAT | 57091 |
rs770430800 | snp | A/G | 3.45644e-05 | 0.00415704 | intron-variant | CASS4 | GRCh38.p7 | 20:56453154 | GAGTTCCAAGTGATC[A/G]AAAAAGGGGCTTCAA | 57091 |
rs770459090 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429074 | GCAGTGTGTCCACCC[C/G]GGCCTAGAGAGGGGA | 57091 |
rs770553944 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432168 | AGGCATATTAGAGTG[G/T]GATTGCAAGGCTAAG | 57091 |
rs770559511 | snp | C/T | 7.07739e-05 | 0.00594827 | intron-variant | CASS4 | GRCh38.p7 | 20:56445864 | ATCATCAGAGTGACA[C/T]TTCCTTTTCCTCTTT | 57091 |
rs770573097 | snp | C/G | 1.64751e-05 | 0.00287007 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452931 | CATTGCCAATGGAAG[C/G]CTCCTTTTTAAGCGG | 57091 |
rs770612500 | snp | A/G | 0.000183537 | 0.00957782 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452412 | TAGCATCGTTTCCTC[A/G]TGCTCCACCACATCC | 57091 |
rs770621600 | snp | A/G | 3.295e-05 | 0.00405881 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56451968 | TCTCACCAGCTTTGC[A/G]GAAGAATCAAGGCCC | 57091 |
rs770656987 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445265 | CTCCATCACTTTCAC[A/G]TTGCCAGGTTCTCTT | 57091 |
rs770674921 | snp | A/G | 1.65282e-05 | 0.00287469 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453034 | CCCCAAAGAGAAACT[A/G]AATCACACCAAAAGA | 57091 |
rs770697950 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436146 | TAGCCAAGTGAGGTG[C/T]GGGCCCAGCAGTCAC | 57091 |
rs770748394 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424991 | AGTAGGGACATGGTT[A/G]TTCTGAATGTTTTCC | 57091 |
rs770870443 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439528 | ATAATAAAAAATAAT[C/T]AGGCAGGCGTGGTGG | 57091 |
rs770901628 | snp | G/T | 1.64746e-05 | 0.00287002 | stop-gained, intron-variant | CASS4 | GRCh38.p7 | 20:56452779 | CTGCTTGAAACAAAG[G/T]AAAGCTTGGATAATC | 57091 |
rs770929057 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56423470 | ACCAAAAAGGGAGAC[C/G]TTATATTTTTGTTTA | 57091 |
rs770991801 | snp | C/G | 1.65996e-05 | 0.00288089 | missense | CASS4 | GRCh38.p7 | 20:56450667 | ACTCCATCCCCCAGA[C/G]AGCCAAGCAAGTGTA | 57091 |
rs771029025 | snp | C/T | 3.73058e-05 | 0.00431874 | intron-variant | CASS4 | GRCh38.p7 | 20:56446042 | TCACCCAGACCTCTG[C/T]GCCCAGAGTCTGGGG | 57091 |
rs771053008 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434896 | CACAAAAACCGAAGG[A/T]TTAACAGCAGTTACC | 57091 |
rs771064174 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428837 | CCTGCTGCTGCATGA[C/T]CAGAGGCAGGTCATT | 57091 |
rs771080322 | snp | C/G | 1.64841e-05 | 0.00287085 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452668 | TTTCTGGATTTTGCC[C/G]GAGGAGTCCATGGGA | 57091 |
rs771085528 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416238 | TATTTTTAGTAGAGA[C/T]GGGTTTTCACCATAT | 57091 |
rs771099025 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434031 | GGGAAACATTTCAAG[C/T]TTCCTTGACAAAGAT | 57091 |
rs771136601 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450062 | TTGAGATGGAGTTTC[A/G]CTCCCGTTGCCCAGG | 57091 |
rs771191551 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447812 | CTCCCTTTGCCATGA[G/T]AGACTCCAGGAGCAC | 57091 |
rs771280540 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56446201 | CTCTAGAAAACATTA[A/T]GACTACTTGAGTTCT | 57091 |
rs771418811 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409923 | AATAACAGACCGAGA[A/G]GTCAAGTTCCTTATT | 57091 |
rs771486642 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458468 | ATTTCACGGCAGCCT[C/T]AGCAGCAGCCAGCCC | 57091 |
rs771493456 | snp | A/G | 4.95176e-05 | 0.00497558 | missense | CASS4 | GRCh38.p7 | 20:56458385 | AGTCAACAGACTCCT[A/G]AGAGGAAACCCCGCT | 57091 |
rs771526401 | snp | A/G | 4.99904e-05 | 0.00499927 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452312 | AGAATTCCGCGGGCC[A/G]TAATTCCTCATGGTT | 57091 |
rs771538684 | in-del | -/GT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436433 | AACCCGTCATATATA[-/GT]GTGTGTGTGTGTATA | 57091 |
rs771669711 | snp | A/G | 1.95238e-05 | 0.00312434 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453118 | AAAAATAGGGCAAAT[A/G]TCTGTGGACAGGTGA | 57091 |
rs771671673 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451987 | GAATCAAGGCCCCAC[A/G]CTCTCCCCAGTTCCA | 57091 |
rs771686285 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428384 | TTTGGGGTAAAGATT[C/G]CCCATTCAGTGAGTC | 57091 |
rs771702297 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443220 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCTTCCA | 57091 |
rs771744378 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429188 | CTGCCTAGAGCTGCC[A/G]TGCCTGCGGATGTCT | 57091 |
rs771753476 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441924 | GTTAACAATCAGTTA[C/G]ACATTTTCTGATCCA | 57091 |
rs771765357 | in-del | -/GT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436435 | CCCGTCATATATAGT[-/GT]GTGTGTGTGTATATA | 57091 |
rs771848841 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447685 | CTCCCTTAGCTCTGG[A/G]GCAGGCAGGTCATTT | 57091 |
rs771958363 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443303 | CCTGGCCAACGTGGT[A/G]CTAAAAATACAAAAA | 57091 |
rs772038216 | snp | A/G | 1.67632e-05 | 0.00289505 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451837 | CAGGGTGTTCCCCTG[A/G]TATCAGTGACTACCT | 57091 |
rs772082389 | snp | A/G | 2.38285e-05 | 0.00345162 | missense | CASS4 | GRCh38.p7 | 20:56458742 | TTCAGAGGGACACTG[A/G]GATGAGGACTGTCTA | 57091 |
rs772122945 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421353 | AAAATTGTAGTGGCA[C/T]GTGGATATGACAGGA | 57091 |
rs772124079 | snp | A/G | 5.66225e-05 | 0.00532053 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56412464 | CATCACCGACATGAA[A/G]GGAACAGGCATCATG | 57091 |
rs772143299 | snp | A/G/T | 5.36738e-05 | 0.0051802 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458675 | CCCCAGCCCTGCCGC[A/G/T]CTGGGGCACCTCCAG | 57091 |
rs772260661 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415007 | TTCCCCTGTCACAGA[C/T]GAGGAAACGAGGCCT | 57091 |
rs772261136 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418696 | GAGACCGCTGGTCGC[C/T]GTGTCGGGTGGGGAG | 57091 |
rs772299114 | snp | A/G | | | utr-variant-5-prime, intron-variant | CASS4 | GRCh38.p7 | 20:56412325 | TTTTGATCGTTTCCC[A/G]TGTGTTGTCAGATAG | 57091 |
rs772311828 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413842 | AAAATATGGGAAGCG[A/T]GGGGGTTATTCAGTA | 57091 |
rs772325603 | snp | A/T | 1.64738e-05 | 0.00286995 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452889 | ACGGATGCTTCCAGA[A/T]GACATCAAGAGGTTT | 57091 |
rs772361440 | snp | C/T | 3.33339e-05 | 0.00408238 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452335 | TCATGGTTCTCCAGA[C/T]GGACAACTTCCCCAT | 57091 |
rs772471393 | snp | A/C | 1.67038e-05 | 0.00288992 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452423 | CCTCGTGCTCCACCA[A/C]ATCCACCGACGACTC | 57091 |
rs772474647 | in-del | -/GTC | | | intron-variant | CASS4 | GRCh38.p7 | 20:56423411 | GGTTTCCAAATGACT[-/GTC]GTCACACCATGGGAA | 57091 |
rs772578168 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56449538 | ATGGGTGCAGCACAC[C/T]AACATGGCAGATGTA | 57091 |
rs772583331 | in-del | -/T | 1.66626e-05 | 0.00288635 | frameshift-variant, intron-variant | CASS4 | GRCh38.p7 | 20:56452368 | CCTGAACCGGACAGA[-/T]TATCAGGTTCCAGTT | 57091 |
rs772592830 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419587 | ATGCACCACTGTGCC[C/T]GGCTAATTTTTGTAT | 57091 |
rs772638460 | snp | C/T | 1.69637e-05 | 0.00291231 | intron-variant | CASS4 | GRCh38.p7 | 20:56445882 | CCTTTTCCTCTTTTC[C/T]CCTCCTTTCTCTCCA | 57091 |
rs772688708 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441964 | CAGGCGTCTCCTCCC[G/T]GCTCATGTCATCTAG | 57091 |
rs772723145 | snp | C/G | 1.71693e-05 | 0.00292991 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437467 | CCAGGCCCCGTTTAT[C/G]AGCAGATGAGGAGTT | 57091 |
rs772751260 | snp | A/G | | | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452159 | TGGATGAAGATGTCA[A/G]CTACAAGGTTCCTTC | 57091 |
rs772772885 | snp | C/T | 3.64924e-05 | 0.0042714 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437528 | AAGTCTATGAATTCC[C/T]CGACCCTCCCACCAG | 57091 |
rs772782871 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443269 | GGTGGATCACTTGAG[A/G]TCAGGAGTTCAAAAC | 57091 |
rs772794452 | snp | G/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410035 | TTTTCTAGTTGAGGT[G/T]GTTTTCCCTAGAAAA | 57091 |
rs772807579 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429218 | TCTTATACCACCATG[A/G]ATGATGAAAGTGTGC | 57091 |
rs772810182 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411327 | TGAGGTGGGTGGATC[A/G]CTTGAGGTCAGGAGT | 57091 |
rs772909743 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447703 | AGGCAGGTCATTTCC[A/G]GCCACATCCTCGTGA | 57091 |
rs772933730 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419753 | GCACTCTTAAAACTC[C/T]TCTAGGAGGCCAGGC | 57091 |
rs773057875 | in-del | -/ACAA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439095 | CTCAATACATATCTG[-/ACAA]ACAAACAAATTAGGA | 57091 |
rs773078792 | snp | C/T | 1.75745e-05 | 0.00296428 | intron-variant | CASS4 | GRCh38.p7 | 20:56450717 | GTGCGGTGTTATGAA[C/T]ACACAAAATCCTCTC | 57091 |
rs773097988 | snp | C/G/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411051 | CTTGTGGGGACGACA[C/G/T]ATGGGACAACCAGAG | 57091 |
rs773136435 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413864 | TATTCAGTAAATCCC[G/T]GCATATCCTTCACCT | 57091 |
rs773155610 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436949 | CCTCGTCTCAGGATA[C/T]AGGTAAGTCTGCCCT | 57091 |
rs773164496 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433624 | TCTGTGAAGGAACAA[C/T]TGGCTGACCCAGAAA | 57091 |
rs773185696 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426255 | CCTCTCTGTGCCTTG[G/T]CTTACTCATCTCCTA | 57091 |
rs773256357 | snp | A/G | 1.90958e-05 | 0.00308991 | missense | CASS4 | GRCh38.p7 | 20:56412477 | AAGGGAACAGGCATC[A/G]TGGACTGTGCGCCCA | 57091 |
rs773309513 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427469 | TCTCTCTGCATTAAT[C/G]TTTCCTAGCCTGTAT | 57091 |
rs773350995 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421483 | GGGAGGATCGCTTGA[A/G]CCCAGCTGTTGGAGA | 57091 |
rs773409368 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431978 | AATTATGACTCTCAT[A/G]CAAATATAAAATGAA | 57091 |
rs773419320 | in-del | -/CA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439828 | GATGTGCACAGGCCT[-/CA]GTCACTGCAGGCATT | 57091 |
rs773419360 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56446644 | TTAGCCCATCCAAAT[G/T]CTCTGCGGTGGCGTT | 57091 |
rs773506967 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444084 | CTGCTTTGTCTGCAT[A/C]CGTGAGTCTAGCCAG | 57091 |
rs773645729 | snp | C/T | 1.65012e-05 | 0.00287234 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452127 | TGGCTTTCTTGTACC[C/T]AGAGGCACATTTCCT | 57091 |
rs773665975 | in-del | -/TG | 1.64819e-05 | 0.00287066 | frameshift-variant, intron-variant | CASS4 | GRCh38.p7 | 20:56452967 | TGAAAAGGAAGAGAC[-/TG]TGCAGTTGACCCCAA | 57091 |
rs773673853 | snp | A/G | 6.9718e-05 | 0.00590374 | intron-variant | CASS4 | GRCh38.p7 | 20:56453155 | AGTTCCAAGTGATCG[A/G]AAAAGGGGCTTCAAT | 57091 |
rs773768954 | snp | C/T | 1.65756e-05 | 0.00287881 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452232 | CAATATTTATGACAT[C/T]CCTAAAGCAACGTCG | 57091 |
rs773788329 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438474 | CTTGGCATATCACCA[A/C]AACAAGCTGCTGTGC | 57091 |
rs773870765 | snp | C/T | 6.59391e-05 | 0.00574153 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451895 | CAAATCCTCAGAAAT[C/T]GGAATGGATTTATGA | 57091 |
rs773879491 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459772 | CCATTCCTGGCATGT[A/G]CGTGTTTTAAATTCA | 57091 |
rs773923602 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409769 | GGATATTATGCAAGC[A/G]CCCAGTTTCCTAGAC | 57091 |
rs773924285 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420055 | ATCTCAAAAACAAAC[A/T]AACAAAAGAAAGCTC | 57091 |
rs773927058 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455087 | ATCTTGATTTGGGGC[C/T]TGTATATCTTCAACA | 57091 |
rs773960659 | snp | C/T | 1.94642e-05 | 0.00311957 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56412491 | CATGGACTGTGCGCC[C/T]AAGGTGAGTGATGTG | 57091 |
rs773990506 | snp | C/T | 1.65299e-05 | 0.00287483 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453037 | CAAAGAGAAACTGAA[C/T]CACACCAAAAGAGTA | 57091 |
rs774000829 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425805 | GTGTTTTTATCTAAT[C/G]CCAAACCTCTAACTC | 57091 |
rs774042931 | snp | A/T | 1.64749e-05 | 0.00287005 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452933 | TTGCCAATGGAAGGC[A/T]CCTTTTTAAGCGGAA | 57091 |
rs774061958 | snp | C/T | 1.76247e-05 | 0.00296851 | intron-variant | CASS4 | GRCh38.p7 | 20:56445867 | ATCAGAGTGACATTT[C/T]CTTTTCCTCTTTTCT | 57091 |
rs774139936 | snp | A/C | 1.64743e-05 | 0.00287 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451973 | CCAGCTTTGCGGAAG[A/C]ATCAAGGCCCCACGC | 57091 |
rs774210512 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439586 | GAGGCTGTGGAAGGA[A/G]GACCCTTTGAGCCCA | 57091 |
rs774236732 | snp | A/G | 1.86795e-05 | 0.00305605 | intron-variant | CASS4 | GRCh38.p7 | 20:56446043 | CACCCAGACCTCTGC[A/G]CCCAGAGTCTGGGGT | 57091 |
rs774266641 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56446380 | ATGGGCATAAGCCAC[C/T]GTGCCCAGCCATTAT | 57091 |
rs774268870 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432781 | TTCTTGTGAAACCCA[C/G]TCCCAACACATTCAA | 57091 |
rs774323796 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445539 | TGGTCCCTAGAGAAC[A/G]TCGGAATCACCTGGC | 57091 |
rs774365582 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56456897 | TCGTATGTTGCCAAG[A/G]CTAGTCTCAAACTCC | 57091 |
rs774376848 | snp | A/T | 1.79855e-05 | 0.00299873 | missense | CASS4 | GRCh38.p7 | 20:56437203 | GACAACTGCCCTGAC[A/T]GCTCTGACGAGCTGG | 57091 |
rs774384306 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425299 | CTAAACTTCTGTGAC[C/T]CTTAATGCACCTGCA | 57091 |
rs774386861 | snp | A/T | 1.65836e-05 | 0.0028795 | missense | CASS4 | GRCh38.p7 | 20:56458602 | TCCGTGGCAGCAGTC[A/T]CCTCTGCAGCCTGCT | 57091 |
rs774460204 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438269 | CACTCCAGCCTCGGT[A/G]GCAGTGAGAACCTGT | 57091 |
rs774509625 | snp | A/T | 1.64754e-05 | 0.00287009 | missense | CASS4 | GRCh38.p7 | 20:56458475 | GGCAGCCTCAGCAGC[A/T]GCCAGCCCGCGGAGA | 57091 |
rs774591273 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416339 | ACAGGCGTGAGCCAC[G/T]GCGCCCAGCCAGAAA | 57091 |
rs774658419 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56451334 | TTTATCTGTGTTGGG[C/G]AAAGGACTTTATCTG | 57091 |
rs774662466 | snp | C/G | 1.66624e-05 | 0.00288633 | splice-donor-variant | CASS4 | GRCh38.p7 | 20:56450680 | GACAGCCAAGCAAGT[C/G]TAAGTATGAAGAGGT | 57091 |
rs774747843 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417570 | ACTCCATGAGGGACA[C/G]ACCTGGGCTTTCTTA | 57091 |
rs774768631 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450273 | AGGTGATCCTCCTGC[C/T]TCAGCCTCCCCAAGT | 57091 |
rs774792011 | snp | C/T | 3.31851e-05 | 0.00407326 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452243 | ACATCCCTAAAGCAA[C/T]GTCGAGTGTTTCTCA | 57091 |
rs774836346 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433327 | TGCTGACTGCTTTGG[A/G]GTAGAGAGAACAGCA | 57091 |
rs774844913 | in-del | -/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435944 | TTTATTAGAGACAGG[-/G]TTTCACCATGTTGGC | 57091 |
rs774911011 | snp | A/C | 3.31076e-05 | 0.0040685 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453053 | CACACCAAAAGAGTA[A/C]CCCTTCCACTAAGCA | 57091 |
rs774926186 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442009 | GCTAAACCCGCCCAG[A/G]AAATACATTCCAAAT | 57091 |
rs774945908 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418807 | TGTACCTTTCATTCC[A/G]TCAACAAATATTGAA | 57091 |
rs774946832 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452787 | AACAAAGGAAAGCTT[A/G]GATAATCGCAATTGG | 57091 |
rs774967764 | snp | A/G | 1.83138e-05 | 0.00302599 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437531 | TCTATGAATTCCCCG[A/G]CCCTCCCACCAGTGC | 57091 |
rs774973418 | snp | A/G | 1.77508e-05 | 0.00297911 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56437214 | TGACTGCTCTGACGA[A/G]CTGGCTTTCAGCAGA | 57091 |
rs774982242 | snp | C/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410087 | TTCTGATCTGTATTA[C/T]GAGCTTAAGGGCAGG | 57091 |
rs775018937 | snp | A/C | 1.6666e-05 | 0.00288664 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452330 | ATTCCTCATGGTTCT[A/C]CAGACGGACAACTTC | 57091 |
rs775059368 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419790 | GCTCATGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 57091 |
rs775091205 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452066 | CACAACTGAATAACA[A/G]TGTGCCCATGCAGAA | 57091 |
rs775091567 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432512 | AGCTGGGACTATAGG[C/T]GTGCACCACCACGCT | 57091 |
rs775104414 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56412818 | CCGCTAATTCCTTCT[G/T]TCTCTGGACCCCAAA | 57091 |
rs775142048 | snp | C/T | 1.97303e-05 | 0.00314082 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56453120 | AAATAGGGCAAATAT[C/T]TGTGGACAGGTGAGT | 57091 |
rs775146098 | snp | C/T | 8.23689e-05 | 0.00641698 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451988 | AATCAAGGCCCCACG[C/T]TCTCCCCAGTTCCAG | 57091 |
rs775229198 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416812 | AGACAGCTATGTGCT[C/T]ATTCAGTTTTCTGAA | 57091 |
rs775284457 | snp | A/G | 4.94458e-05 | 0.00497197 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452669 | TTCTGGATTTTGCCC[A/G]AGGAGTCCATGGGAC | 57091 |
rs775410050 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457456 | GGGAGAAGTTGGTTC[A/C]ATTTTCCAGAAAATA | 57091 |
rs775410880 | snp | C/T | 1.66657e-05 | 0.00288662 | missense | CASS4 | GRCh38.p7 | 20:56437342 | GCCTCCAAATCCTCA[C/T]GGAGGTCGCTGCAGA | 57091 |
rs775433495 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445363 | CTCAGCCCAGGTGAC[A/G]AGTCCTTAGACAGCT | 57091 |
rs775515761 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436753 | TTAGCCCGGGGTGGC[A/G]GCACGCATGTGTAGT | 57091 |
rs775600435 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56446561 | TTTTTTAACTTGTTT[G/T]TATATAAGTGGAATA | 57091 |
rs775709837 | in-del | -/TA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436358 | GTGTGTGTGTGTGTG[-/TA]TGTATATATATATAT | 57091 |
rs775714539 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417447 | GTGCAAATCACTTCC[C/G]CCCTACACAGGCCCA | 57091 |
rs775742621 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428334 | CCTCAAACTGTGGGG[C/T]AGCTTAGACATAGTC | 57091 |
rs775776673 | snp | A/G | 1.66674e-05 | 0.00288676 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452336 | CATGGTTCTCCAGAC[A/G]GACAACTTCCCCATC | 57091 |
rs775780911 | snp | A/G | 1.88988e-05 | 0.00307393 | missense | CASS4 | GRCh38.p7 | 20:56412466 | TCACCGACATGAAGG[A/G]AACAGGCATCATGGA | 57091 |
rs775870009 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428388 | GGGTAAAGATTGCCC[A/G]TTCAGTGAGTCCTGC | 57091 |
rs775905132 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56449550 | CACCAACATGGCAGA[C/T]GTATACATATGTAAC | 57091 |
rs775937409 | snp | C/G | 1.88195e-05 | 0.00306747 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437560 | GCCAGAATCATCTGT[C/G]AAAAGACTCTCAGCT | 57091 |
rs775960291 | snp | A/G | 6.59076e-05 | 0.00574016 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452945 | GGCTCCTTTTTAAGC[A/G]GAACTGTGAAAAGGA | 57091 |
rs775977650 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445318 | AAAGCTGCCAGCTGC[A/G]GCTCAACTGGTCACC | 57091 |
rs775994936 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426377 | AGAGTTGAGAACCCG[C/T]GAGCTATCCTGATTC | 57091 |
rs776095229 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56430868 | GCATTTGAGAAAAGT[A/G]AGAAAACAATGTGAC | 57091 |
rs776146546 | snp | A/T | 1.64958e-05 | 0.00287187 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452100 | ACTCAGCCTTCCAGA[A/T]ATTCCTTCTTATGGC | 57091 |
rs776166763 | in-del | -/AT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431039 | TTTTATGTGTATAAA[-/AT]AAAATATTCTGGCTA | 57091 |
rs776170142 | snp | C/T | 1.68932e-05 | 0.00290625 | intron-variant | CASS4 | GRCh38.p7 | 20:56445884 | TTTTCCTCTTTTCTC[C/T]TCCTTTCTCTCCAAG | 57091 |
rs776239270 | snp | C/T | 8.55059e-05 | 0.00653801 | intron-variant, synonymous-codon | CASS4 | GRCh38.p7 | 20:56437460 | TCCCACTCCAGGCCC[C/T]GTTTATGAGCAGATG | 57091 |
rs776282798 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455566 | TGCTATTTTGTTCAA[A/C]ATTAAGTAGGCCTTA | 57091 |
rs776282910 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56412786 | TCCTGAAGCAAGATG[C/T]GAGTCTGCCTCAGCC | 57091 |
rs776292360 | snp | A/G | 5.00204e-05 | 0.00500077 | missense | CASS4 | GRCh38.p7 | 20:56437353 | CTCACGGAGGTCGCT[A/G]CAGACAGGCCGTGCC | 57091 |
rs776353812 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442473 | CTTTCTGATGAACAC[G/T]TTACTGAAATTTCAC | 57091 |
rs776368745 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417302 | ACCTGGCCCTTCAGG[A/G]CCCATTAGATCCCAC | 57091 |
rs776443719 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443907 | ATGCTTCATTCTTAC[C/T]GAGAGCGCTTTGGAA | 57091 |
rs776510043 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421756 | CTTCTAATTGGTGTC[A/G]GCATAATTGCTTACG | 57091 |
rs776591556 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415495 | GAGCTGTAAGTAAAG[A/G]TCTGTTGAGCTTCTT | 57091 |
rs776674677 | snp | C/T | 6.77587e-05 | 0.0058202 | intron-variant | CASS4 | GRCh38.p7 | 20:56450705 | AGAGGTGCTAAGGTG[C/T]GGTGTTATGAACACA | 57091 |
rs776675066 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447903 | ATCCCAGCACTTTGG[A/G]AGGCTGAGGCAGGTA | 57091 |
rs776727889 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416246 | GTAGAGACGGGTTTT[C/T]ACCATATTGGCCAGG | 57091 |
rs776766891 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450108 | GCGATCTTGGCTTAC[C/T]GCAACCTCCACCTCC | 57091 |
rs776772025 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411734 | AGAGAGAGAATACAG[A/G]TGCGGGGCTCAGCAT | 57091 |
rs776832429 | snp | A/C | 1.65866e-05 | 0.00287976 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452543 | TGGTCAGCTCTGTCG[A/C]TGGCCTGATGCTCTT | 57091 |
rs776911499 | snp | C/T | 1.8434e-05 | 0.0030359 | missense | CASS4 | GRCh38.p7 | 20:56437165 | CTCTCCACCCACAGG[C/T]ACTCCTGGCCAGGGC | 57091 |
rs777110089 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440111 | CTACAAGACATAGAA[C/T]CAGACAGTTGTTACA | 57091 |
rs777110173 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426472 | CACTCCTTTCAGGGC[G/T]AACAGAATGGTTTTG | 57091 |
rs777136930 | in-del | -/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428588 | CACCCAAATGTCTTA[-/C]GCCTGGCCTGTCTCA | 57091 |
rs777190081 | snp | A/T | 2.17351e-05 | 0.00329653 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56453128 | CAAATATCTGTGGAC[A/T]GGTGAGTTCAGAGTT | 57091 |
rs777340688 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427944 | AAATGTCCTTCTTGG[C/T]CTTGGAGATCTACAT | 57091 |
rs777385899 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450912 | GGTAGTGGGCGCCTG[C/T]AATCCCAGCACTTTG | 57091 |
rs777415327 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457209 | AATCAGTTTTATGCC[C/T]TATCTGTCTGAATGC | 57091 |
rs777442989 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432101 | AACTTGAATGAATTT[-/A]TTTTTAAAAAGAGAT | 57091 |
rs777467395 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425360 | CCTCTCTGTGTGGTT[C/G]CACTCTGTGGCCCTA | 57091 |
rs777567822 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413399 | CTAGTGTGGCTGTCT[A/G]CGGTGGCTCACACCT | 57091 |
rs777579582 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56417040 | AAATGTAGAATTTTT[A/T]AAAAAATCTTCCACA | 57091 |
rs777597630 | snp | A/G | 6.6084e-05 | 0.00574784 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56453030 | GCCTCCCCAAAGAGA[A/G]ACTGAATCACACCAA | 57091 |
rs777600668 | snp | A/G | 3.33634e-05 | 0.00408418 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452404 | AGCAGAGCTAGCATC[A/G]TTTCCTCGTGCTCCA | 57091 |
rs777614639 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425776 | CCAACTGTACAAATG[A/C]ACATGGACTCAAAGT | 57091 |
rs777624719 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429639 | ACTCATACTCACACA[C/T]GCCCCCTCACCCACG | 57091 |
rs777652554 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56410896 | CATTGTTCCCTCCCT[A/G]TTATCTGCTATCGCC | 57091 |
rs777740575 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56448331 | ACTATGATGATTGAG[-/T]TTTTTTGGTGCCCTC | 57091 |
rs777823212 | snp | A/C | 1.64746e-05 | 0.00287002 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56451962 | CACGCCTCTCACCAG[A/C]TTTGCGGAAGAATCA | 57091 |
rs777828565 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452766 | CTCCTACCGCATCCT[A/G]CTTGAAACAAAGGAA | 57091 |
rs777833029 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436003 | GTGATCTGCCCTCCT[C/T]GGCCCCCCAAAGTGC | 57091 |
rs777847231 | snp | A/G | 2.27534e-05 | 0.00337286 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458738 | GCAGTTCAGAGGGAC[A/G]CTGGGATGAGGACTG | 57091 |
rs777964506 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440792 | TGTGCAGGCTGTGGC[A/G]AACAACAGAAACCGC | 57091 |
rs777975018 | snp | C/G | 3.36927e-05 | 0.00410429 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437434 | TATCAGGTGCCCACT[C/G]TACCCCGCCCTCCCA | 57091 |
rs778018372 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439994 | GAATGTGCTACTCAC[C/T]ATTCAGGCCTTCTCC | 57091 |
rs778074357 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434128 | GCAGTCTCATTCACC[A/G]TGGGTGGAGGTGTGA | 57091 |
rs778074431 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419656 | GGCTGGTCTCGAACT[C/T]CTGTTTTTAAGTGAT | 57091 |
rs778120970 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433249 | GTCAGGGACCCTTTT[C/T]CTAAGGAAGTGACAT | 57091 |
rs778152567 | in-del | -/AAGTGAGAG | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443091 | AAGCTTGGTGTGTTT[-/AAGTGAGAG]CTGGGAGGTACCACT | 57091 |
rs778196586 | snp | A/G | 0.000151432 | 0.00870018 | utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56412448 | CAGGGGAGCTGCTCC[A/G]CATCACCGACATGAA | 57091 |
rs778255229 | snp | A/C | 1.64732e-05 | 0.0028699 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452866 | CTTGAGAGGTTTGTC[A/C]TGGTGGCACGGATGC | 57091 |
rs778336723 | snp | A/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56409637 | GTCTCAGAAAAGAAA[A/T]TTCGGTCCAAACTAC | 57091 |
rs778363722 | in-del | -/CTAT | 0.00199996 | 0.0315592 | intron-variant | CASS4 | GRCh38.p7 | 20:56458311 | CATTGATTGAATCTC[-/CTAT]CTATTTTCTTCCTTC | 57091 |
rs778458905 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427721 | TGTATCAAAAGATCT[A/G]TGATATTTATAGTAT | 57091 |
rs778475514 | in-del | -/TCTT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432692 | ACCTTTAATCAATAC[-/TCTT]TATAAGACTCTAAAA | 57091 |
rs778623606 | snp | A/G | 1.67638e-05 | 0.0028951 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452494 | TTGGACCTGGATGTG[A/G]CCAAGGAGACAGTGA | 57091 |
rs778640144 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414929 | GAGGCCCTGTGCTGA[C/G]TGCTCTACTTGCATT | 57091 |
rs778684555 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56422769 | CCAGTTAAAGTTTGC[A/G]TTTATTCACAGCATG | 57091 |
rs778711376 | snp | C/T | 1.65211e-05 | 0.00287407 | | | GRCh38.p7 | 20:56445940 | TCCGGGCCTCACTGC[C/T]GACTCTGCCTTCCCA | 57091 |
rs778727445 | snp | C/T | | | | | GRCh38.p7 | 20:56428741 | AGTAGGAAACAGACT[C/T]GGACTTGGAAAGGCC | 57091 |
rs778745360 | snp | A/G | 6.59239e-05 | 0.00574087 | | | GRCh38.p7 | 20:56452054 | GGTCCCTCACTCCAC[A/G]ACTGAATAACAATGT | 57091 |
rs778834869 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56453642 | GCCTGTAATTCCAAC[A/G]CTTTGGGAGGCCAAC | 57091 |
rs778841810 | in-del | -/TG | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436338 | ATTGCTATATATATG[-/TG]TGTGTGTGTGTGTGT | 57091 |
rs778849022 | snp | A/T | 1.7179e-05 | 0.00293074 | intron-variant | CASS4 | GRCh38.p7 | 20:56458320 | AATCTCCTATCTATT[A/T]TCTTCCTTCCCTTCT | 57091 |
rs778977913 | snp | A/G | 1.74485e-05 | 0.00295363 | intron-variant | CASS4 | GRCh38.p7 | 20:56451796 | AGCTACTAACCCGGC[A/G]ACTATGTGTGGTTCT | 57091 |
rs778992928 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452781 | GCTTGAAACAAAGGA[A/G]AGCTTGGATAATCGC | 57091 |
rs779035230 | snp | G/T | 0.000115305 | 0.00759205 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452879 | TCATGGTGGCACGGA[G/T]GCTTCCAGAAGACAT | 57091 |
rs779056437 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419446 | GTGTGGGAGATCCTG[C/T]ACTTCCCCCACACCA | 57091 |
rs779061119 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447449 | TGGGTGGTCTCAGAC[G/T]CCTGCAGGGCTGCAA | 57091 |
rs779070051 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439763 | GGAGAAAAAGAATGC[A/G]CTATTTCCCTCAAAG | 57091 |
rs779074764 | snp | A/G | | | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452060 | TCACTCCACAACTGA[A/G]TAACAATGTGCCCAT | 57091 |
rs779192024 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424631 | CTGTAGTCCCAGCTA[A/C]TCGGGAAGCTGAGGC | 57091 |
rs779217328 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445699 | TCGTGGGCCACGTGC[A/G]AGGAAGGCTGCCTCC | 57091 |
rs779270478 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445136 | AAGGTTTATATGTAT[A/G]TAAATTGGATGGTCA | 57091 |
rs779371627 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414045 | GTGTCTCCTAAGAAC[A/G]AGGACATTCATCTAC | 57091 |
rs779398752 | snp | C/G | 1.64751e-05 | 0.00287007 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56451935 | GTCTCCAGGAAAGGC[C/G]AGCGTCAGAAACACG | 57091 |
rs779403276 | snp | C/T | 3.71616e-05 | 0.00431038 | intron-variant | CASS4 | GRCh38.p7 | 20:56437122 | AGCAGTCACTGGCCA[C/T]GGTGCTAACTGCAAA | 57091 |
rs779453757 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433136 | TTACGTTCTTATGGG[G/T]AGACAGACCCTGGAT | 57091 |
rs779492090 | snp | A/C | 1.76861e-05 | 0.00297368 | intron-variant | CASS4 | GRCh38.p7 | 20:56446021 | GCCTTGTTCAGGGGC[A/C]CCTCATCACCCAGAC | 57091 |
rs779493901 | snp | A/G | 6.59402e-05 | 0.00574158 | synonymous-codon | CASS4 | GRCh38.p7 | 20:56458567 | GGAGACCCAGGAGAG[A/G]GACGTGCGCAACGAG | 57091 |
rs779558911 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56415864 | GGCAGATTTTGTGTA[A/G]TATCCAGACTGATTT | 57091 |
rs779685468 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432986 | TCTTACCTCTTAAAG[A/G]CTTGAAAATGGGGGC | 57091 |
rs779725157 | snp | G/T | 3.34644e-05 | 0.00409036 | missense | CASS4 | GRCh38.p7 | 20:56458347 | TTCTTTAGAATCCTG[G/T]CCCTCTTATACCTCA | 57091 |
rs779736863 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56446112 | TGGCGGCCAGGGGCT[C/T]AGCCTCCAGAATACA | 57091 |
rs779785410 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56439669 | CCTGGGTGACTGACC[A/G]GGACCCTGTCTTAAA | 57091 |
rs779787409 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425951 | AAAAATTTAATACTA[C/T]ATTTTGGAGATTGTC | 57091 |
rs779796666 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447578 | ATTCCTGTAAGTGCC[-/T]CCCCACCTCCTACCC | 57091 |
rs779817244 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434245 | CCATGGAAATAAATA[A/C]GGGGAGTTGCAAATA | 57091 |
rs779838692 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56438060 | TCTGGGGGGACGAGA[C/T]AGGAGGATCATTTGA | 57091 |
rs779858371 | snp | A/G | 1.69723e-05 | 0.00291305 | intron-variant, missense | CASS4 | GRCh38.p7 | 20:56437449 | CTACCCCGCCCTCCC[A/G]CTCCAGGCCCCGTTT | 57091 |
rs779877573 | snp | G/T | 1.65291e-05 | 0.00287476 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452196 | TCTGATTCCCCGAGT[G/T]GAACAGCAGAACACC | 57091 |
rs779915566 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56453266 | TCTAGAAAATAAAAT[C/T]TATGAAAGTAAAATT | 57091 |
rs779969415 | snp | C/G | 1.6623e-05 | 0.00288292 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452263 | AGTGTTTCTCAGGCT[C/G]GGAAGGAGCTGGAGA | 57091 |
rs780009166 | in-del | -/TACGCA | 3.82387e-05 | 0.0043724 | intron-variant, splice-donor-variant | CASS4 | GRCh38.p7 | 20:56437588 | GCTTTCCAAAACAGG[-/TACGCA]TACTTCCACCTACTA | 57091 |
rs780016534 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56426813 | AAACTCCTGAGTTCA[A/G]AGTGATCTGCTCACC | 57091 |
rs780046527 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441036 | CTCTGTCACCCAGGC[C/T]GGAGTGCAGTGGCGT | 57091 |
rs780121116 | snp | C/T | 3.7046e-05 | 0.00430367 | intron-variant | CASS4 | GRCh38.p7 | 20:56437147 | TGCAAATTCTCTTCT[C/T]CCCTCTCCACCCACA | 57091 |
rs780161415 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56451193 | AACTTCTCTGTTTTT[A/G]TGGGCTGGGAGTATT | 57091 |
rs780186385 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56431662 | AAACCCCATTGTTCT[C/T]TGGGAAAAAGTCCTT | 57091 |
rs780212117 | snp | C/T | | | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56451989 | ATCAAGGCCCCACGC[C/T]CTCCCCAGTTCCAGC | 57091 |
rs780251154 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56442770 | TCCTGGTGAAACTGC[A/T]TTTGGATCCACTAGT | 57091 |
rs780285783 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56424506 | AGCACTTTGGGAGGT[C/T]AAGGCGGGTGGATCA | 57091 |
rs780303983 | in-del | -/GT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56436434 | AACCCGTCATATATA[-/GT]GTGTGTGTGTATATA | 57091 |
rs780336316 | snp | C/T | 1.65919e-05 | 0.00288022 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56451852 | ATATCAGTGACTACC[C/T]TAAGAAGAGGCGGTT | 57091 |
rs780405743 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452027 | TCTACAATCCTCCAA[A/G]TGGCAGATCCAGGTC | 57091 |
rs780424071 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443102 | TGTTTCTGGGAGGTA[A/C]CACTGGCGGTACAGC | 57091 |
rs780438181 | snp | A/C | | | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56453096 | ACACTCTTCTGAACT[A/C]TTAAAGAAAAATAGG | 57091 |
rs780472470 | snp | A/G | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411259 | CTAAATAAAAATGCA[A/G]GCCGGGGCCAGGCGT | 57091 |
rs780473214 | snp | G/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56419232 | TGCCACGGAGGGGGA[G/T]ATTAGAACACTCCAA | 57091 |
rs780576064 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425855 | CCCAGAAGGGACCCT[C/T]AGTGAGTGACATAAT | 57091 |
rs780584584 | snp | C/T | 1.65272e-05 | 0.0028746 | missense | CASS4 | GRCh38.p7 | 20:56445946 | CCTCACTGCCGACTC[C/T]GCCTTCCCAGGTGTA | 57091 |
rs780598301 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56457339 | GCTAATGGAATAGCC[A/G]GAGGCAGCCTTTTCT | 57091 |
rs780639827 | snp | A/G | 6.66012e-05 | 0.00577028 | synonymous-codon, intron-variant | CASS4 | GRCh38.p7 | 20:56452529 | TCTGCAGCACAAGGT[A/G]GTCAGCTCTGTCGCT | 57091 |
rs780670482 | snp | A/C | | | intron-variant | CASS4 | GRCh38.p7 | 20:56445033 | GAGAATCGCTTGAAT[A/C]CAGGAGGCGGAGTTT | 57091 |
rs780796158 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56413502 | ACATGAAAAAACCCC[A/T]TATCTACCAAAAATA | 57091 |
rs780870845 | snp | C/T | 1.66763e-05 | 0.00288753 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452303 | AGGTGTCAGAGAATT[C/T]CGCGGGCCATAATTC | 57091 |
rs780914643 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | CASS4 | GRCh38.p7 | 20:56459554 | CTCGGTCAGGAATCA[C/T]TTAATCCTGGAAGTC | 57091 |
rs780985837 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450761 | GCTTGGGGCCAGGCA[C/T]GGTGGCTGAAGCCTG | 57091 |
rs781026591 | snp | A/G | 1.77651e-05 | 0.00298031 | intron-variant, synonymous-codon | CASS4 | GRCh38.p7 | 20:56437499 | GGCGGAGGGGCCCCA[A/G]CCCCCTACTGCCCAA | 57091 |
rs781029185 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56414567 | CAGGTGCACACCACC[A/G]AGCCCCACTGCAATT | 57091 |
rs781052214 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56437999 | CATTTAAAATGTATA[C/T]TCCAGGCTGGGCATG | 57091 |
rs781114746 | snp | C/T | 1.92421e-05 | 0.00310172 | intron-variant | CASS4 | GRCh38.p7 | 20:56437627 | ATGGGTTGAGGGGTA[C/T]GGAAACACCCAGAGG | 57091 |
rs781182932 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427169 | ATAGCAAGACCCTGT[C/G]TCTTAAAAAAAAAAA | 57091 |
rs781242436 | snp | G/T | 4.94645e-05 | 0.00497291 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452905 | GACATCAAGAGGTTT[G/T]CCTCCATTGTCATTG | 57091 |
rs781243568 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425031 | CACACATGCAACATG[C/T]AGCTACTGTGTCCTG | 57091 |
rs781260823 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56421893 | GAAAAGCACCTGCAT[A/G]TTATTTTCTCTGTAA | 57091 |
rs781311379 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56425033 | CACATGCAACATGCA[A/G]CTACTGTGTCCTGAT | 57091 |
rs781383101 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56429869 | TTTTTTCATAACTTC[C/T]TGTATTTTTTATAAC | 57091 |
rs781391496 | snp | A/G | 3.29549e-05 | 0.00405911 | missense, intron-variant | CASS4 | GRCh38.p7 | 20:56452039 | CAAGTGGCAGATCCA[A/G]GTCCCTCACTCCACA | 57091 |
rs781416926 | snp | A/C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435624 | CAAGGCGACTTTTTT[A/C/T]AGAACTGTGTGGCTA | 57091 |
rs781439968 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428847 | CATGACCAGAGGCAG[A/G]TCATTAATCTCTCCT | 57091 |
rs781529808 | snp | A/G | 1.65696e-05 | 0.00287828 | missense | CASS4 | GRCh38.p7 | 20:56450651 | GCCCCAAGAAGGCAG[A/G]ACTCCATCCCCCAGA | 57091 |
rs781558688 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56418154 | GGTTTCAGGTGGTGA[A/G]AACTGCCAGAAAGAG | 57091 |
rs781570933 | snp | A/T | 3.32901e-05 | 0.0040797 | missense | CASS4 | GRCh38.p7 | 20:56437323 | GGCCTGGCCCCTGCC[A/T]ACCGCCTCCAAATCC | 57091 |
rs781650613 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56433166 | TGAGTTGAACCCTAA[C/T]GTGACACGTACTGAT | 57091 |
rs781693964 | snp | C/T | | | upstream-variant-2KB | CASS4 | GRCh38.p7 | 20:56411193 | GCTATCCCCCACAGC[C/T]GGTTGGGGATAGAAC | 57091 |
rs781739897 | snp | C/T | 1.77707e-05 | 0.00298077 | intron-variant | CASS4 | GRCh38.p7 | 20:56446025 | TGTTCAGGGGCCCCT[C/T]ATCACCCAGACCTCT | 57091 |
rs781757632 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56455837 | TCGGGAGGCTGAGGC[A/T]GGAGAATTGCTTGAA | 57091 |
rs796132816 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56441379 | GGAGGCCAAGGCGGG[C/T]GGATCACCTGAGGTC | 57091 |
rs796139788 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56440560 | TACAATGACAGGCTC[C/G]TACAAGGTACTTAGT | 57091 |
rs796163846 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56427708 | TTCACATTTCCCATG[C/T]ATCAAAAGATCTGTG | 57091 |
rs796169311 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432903 | GTGTGGGCAGGGGCG[-/T]CACAGAAATCTTCCC | 57091 |
rs796189582 | in-del | -/TT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420556 | ACCATGCCCATCTAA[-/TT]TTTTTTTTTTTTTTT | 57091 |
rs796240310 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56444836 | TAAATCGGGGCCAGG[C/T]GCGGTGGCTCACGCC | 57091 |
rs796260869 | in-del | -/GT | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416557 | TGTGTGTGTGTGTGT[-/GT]ATGCACACATGCCAT | 57091 |
rs796465072 | in-del | -/A | | | intron-variant | CASS4 | GRCh38.p7 | 20:56451021 | TAAAATACAAAAATT[-/A]AAAAAAAAAAAAAAG | 57091 |
rs796538136 | snp | C/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56447696 | CTGGGGCAGGCAGGT[C/G]ATTTCCAGCCACATC | 57091 |
rs796541489 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416113 | GGAGTGCAGTGGCAT[A/G]ATCTTGGCTCACTGC | 57091 |
rs796587796 | in-del | -/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56428944 | CCCCAGCCCTGACAT[-/T]CTTGAGTTTCTGCAG | 57091 |
rs796611067 | multinucleotide-polymorphism | CG/GA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56432901 | AGTGTGGGCAGGGGC[CG/GA]CACAGAAATCTTCCC | 57091 |
rs796627588 | in-del | -/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56435282 | TCAACAAACATAATG[-/G]AAGAGTTGGTCACTT | 57091 |
rs796676544 | snp | C/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56443106 | TCTGGGAGGTACCAC[C/T]GGCGGTACAGCCAGT | 57091 |
rs796737210 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56434162 | GATTGAACTTTGCTG[A/G]AGGGCAACGTGACAG | 57091 |
rs796779135 | snp | A/T | | | intron-variant | CASS4 | GRCh38.p7 | 20:56450211 | TAATTTTGTATTTTT[A/T]ATAGAGTTCTCCATG | 57091 |
rs796937974 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | CASS4 | GRCh38.p7 | 20:56411679 | GCATGAGCTAGCAGG[C/G]GTTTCAAGTACAACA | 57091 |
rs796978686 | in-del | -/TA | | | intron-variant | CASS4 | GRCh38.p7 | 20:56416558 | GTGTGTGTGTGTGTG[-/TA]TGCACACATGCCATT | 57091 |
rs797012175 | snp | A/G | | | intron-variant | CASS4 | GRCh38.p7 | 20:56420450 | CTGGAGTGCAGTGGC[A/G]TTATCATAGTTCACT | 57091 |