SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1043378 | snp | A/C | | | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68291300 | AAAGGACTTTTAATC[A/C]CAGACAGTAGAATTA | 10116 |
rs1227308 | snp | A/G | 0 | 0 | intron-variant | FEM1B | GRCh38.p7 | 15:68285956 | tggtattctgttcca[A/G]aaattgtgatcaaca | 10116 |
rs1228663 | snp | G/T | 0 | 0 | intron-variant | FEM1B | GRCh38.p7 | 15:68286044 | tataggtctatactg[G/T]gtctctaatttttgt | 10116 |
rs1228664 | snp | G/T | 0 | 0 | intron-variant | FEM1B | GRCh38.p7 | 15:68286068 | tttttgtatgtactg[G/T]gaggtaggaatcaag | 10116 |
rs1236841 | snp | A/G | 0 | 0 | intron-variant | FEM1B | GRCh38.p7 | 15:68285985 | cactaaattcattaa[A/G]aatagtctatggctt | 10116 |
rs3759822 | snp | A/G | 0.100588 | 0.200439 | upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68275974 | TAGAGATATGGAGAG[A/G]CAGAGAGAGATAGAA | 10116 |
rs3837688 | in-del | -/AGTCC | | | upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68276443 | AGCCGAGCCCAGTCC[-/AGTCC]CTTGGAGCCACATAA | 10116 |
rs3837689 | in-del | -/GTTT | | | intron-variant | FEM1B | GRCh38.p7 | 15:68288883 | AAAGTGAACATATTT[-/GTTT]ACTAGAGTCCCCTTT | 10116 |
rs6494729 | snp | C/T | 6.58892e-05 | 0.00573936 | synonymous-codon | FEM1B | GRCh38.p7 | 15:68290837 | GCATCTGGCTGTCAA[C/T]TCCAATACTCCAGTT | 10116 |
rs6494730 | snp | G/T | 0.368119 | 0.220336 | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68292218 | AAGGAACCAGGATAT[G/T]TTTGAATTTTTTCAC | 10116 |
rs7172290 | snp | A/T | | | intron-variant | FEM1B | GRCh38.p7 | 15:68280209 | GTGGCAATTAAAAGA[A/T]CCTGAAATGACTAGA | 10116 |
rs7172340 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | FEM1B | GRCh38.p7 | 15:68288463 | CTAGCACAGTAGACT[A/G]TCTCCAGCAAAAATC | 10116 |
rs7174574 | snp | C/T | 0.299411 | 0.245069 | intron-variant | FEM1B | GRCh38.p7 | 15:68289052 | tgttatctgttcata[C/T]tgtgtgtggagcagt | 10116 |
rs7174848 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | FEM1B | GRCh38.p7 | 15:68283776 | AATCAGTTTGGAAAC[A/G]TTCTTTAAATTGAAA | 10116 |
rs7175297 | snp | A/G | 0.368938 | 0.219895 | intron-variant | FEM1B | GRCh38.p7 | 15:68284190 | gtgcccagccCTCAT[A/G]TAAACTTTTTAGTTA | 10116 |
rs8027628 | snp | G/T | 0.271702 | 0.249056 | intron-variant | FEM1B | GRCh38.p7 | 15:68285991 | attcattaagaatag[G/T]ctatggctttttttt | 10116 |
rs10152450 | snp | G/T | 0.368529 | 0.220116 | intron-variant | FEM1B | GRCh38.p7 | 15:68279141 | AGTGGGCTGCTGGGC[G/T]TTAATGTCAAAATAA | 10116 |
rs11630865 | snp | A/G | 0.299664 | 0.245017 | intron-variant, utr-variant-5-prime | FEM1B | GRCh38.p7 | 15:68278826 | CACTTCATCTTCCAG[A/G]GCTAATAATCCATCC | 10116 |
rs11632503 | snp | C/T | 0 | 0 | intron-variant | FEM1B | GRCh38.p7 | 15:68280332 | aacacctactgcgtg[C/T]taggttctgtGGTAG | 10116 |
rs11636081 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | FEM1B | GRCh38.p7 | 15:68287727 | tcaaggtgccagtag[A/G]ttcagttgtctggtg | 10116 |
rs12594282 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68295329 | CAAGCTTGCCAAATG[A/T]TGAAATGAACAAGAT | 10116 |
rs12909277 | snp | A/G | 0.445724 | 0.155538 | intron-variant | FEM1B | GRCh38.p7 | 15:68288574 | GATCAGACTCTAGCA[A/G]TAGTCTAATTTTGTA | 10116 |
rs16951723 | snp | C/T | 0.368324 | 0.220226 | upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68277673 | AGCAGAACCTTTCTC[C/T]ACCGGGCCCGCGTGT | 10116 |
rs28498450 | snp | C/T | | | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68294590 | TAAGCAGAAGCGTTT[C/T]TTTTTTTTTTTTGGA | 10116 |
rs28728467 | snp | C/G | | | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68294902 | GCTGTGTGTCCATTC[C/G]TACTCTGAAAATGCA | 10116 |
rs34021140 | snp | C/T | 0.0367231 | 0.130434 | synonymous-codon | FEM1B | GRCh38.p7 | 15:68291044 | TAGCCTAGTTGAAGC[C/T]GGAGCTCACACTGAC | 10116 |
rs34503084 | in-del | -/T | | | intron-variant | FEM1B | GRCh38.p7 | 15:68286682 | TAGAAGTCTTGTGCA[-/T]TTTTTCATTAGATTT | 10116 |
rs34601322 | in-del | -/C | 0.0279526 | 0.114869 | intron-variant | FEM1B | GRCh38.p7 | 15:68285785 | CAGTCCTCTTCTTAG[-/C]CCCCCCCGCAGTGCT | 10116 |
rs34693034 | snp | C/T | 0.299664 | 0.245017 | intron-variant | FEM1B | GRCh38.p7 | 15:68282497 | TGAACCAGGCATTTC[C/T]ATTTCAGATTGAACC | 10116 |
rs34728807 | in-del | -/C | | | intron-variant | FEM1B | GRCh38.p7 | 15:68284875 | TGTAAGGGGGAGATT[-/C]CCCTGCACAAGCTCA | 10116 |
rs34917142 | snp | A/C/G | 0.00683764 | 0.0580695 | synonymous-codon | FEM1B | GRCh38.p7 | 15:68290021 | TGGCCATGGGATGAC[A/C/G]CCATTGAAAGTAGCT | 10116 |
rs34999248 | in-del | -/T | | | intron-variant | FEM1B | GRCh38.p7 | 15:68285928 | TTTAACGGTTAATGC[-/T]TTTTTTTTTTTTTGG | 10116 |
rs35187853 | in-del | -/T | 0.32955 | 0.237006 | intron-variant | FEM1B | GRCh38.p7 | 15:68283886 | TAATCTCACGTAAAC[-/T]TTTTTTTTTTTTTTT | 10116 |
rs35242796 | snp | A/C | | | intron-variant | FEM1B | GRCh38.p7 | 15:68286162 | TTCTACCTGAATTTC[A/C]CTGGAGCCTTTGTCA | 10116 |
rs35278866 | in-del | -/C | | | utr-variant-5-prime, upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68278302 | GCGGCGGCGACGGCG[-/C]CCCTGTTGAATGGGC | 10116 |
rs35445025 | in-del | -/G | | | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68293430 | TTATTTATAAAATGA[-/G]GAATAATGATTATAT | 10116 |
rs35486786 | in-del | -/A | | | intron-variant | FEM1B | GRCh38.p7 | 15:68288932 | TCACTACCTCTCCCC[-/A]AAAGTAACCAGTATC | 10116 |
rs35525989 | snp | C/G/T | 0.00675318 | 0.0577161 | synonymous-codon, utr-variant-5-prime | FEM1B | GRCh38.p7 | 15:68289730 | AACTAATTCAACCCC[C/G/T]CTGCGGGCAGCATGC | 10116 |
rs35576212 | snp | C/T | 0.163892 | 0.234703 | intron-variant | FEM1B | GRCh38.p7 | 15:68286789 | ACATAATCATGACAA[C/T]AAAAACATAACAAAA | 10116 |
rs35599421 | snp | A/G | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68277949 | AGGGCGGAAAGCGCA[A/G]GAGGAGGCAGTGTTA | 10116 |
rs35606342 | snp | C/T | 0.00927954 | 0.0674808 | synonymous-codon, upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68278456 | ATACAAGGCGGCCAG[C/T]GAGGGCAAGGTGCTG | 10116 |
rs35616110 | in-del | -/C | | | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68292108 | TTGTCCCCTTTTCCC[-/C]TTTTTCTCCTGTATC | 10116 |
rs35616559 | in-del | -/T | | | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68294500 | AATTAAAATTTCAAG[-/T]TGAGCAACACCCTGT | 10116 |
rs35629462 | in-del | -/C | | | intron-variant | FEM1B | GRCh38.p7 | 15:68283808 | AATGTTTGAACAATG[-/C]ATGTGTACTATGTTT | 10116 |
rs35888855 | in-del | -/A | | | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68292366 | AAATTTTTCAACCAC[-/A]AAAATGTCACTTATT | 10116 |
rs35987978 | in-del | -/A | | | frameshift-variant, upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68278449 | CTATGTATACAAGGC[-/A]GGCCAGCGAGGGCAA | 10116 |
rs55700060 | snp | A/G | 0.368733 | 0.220005 | intron-variant | FEM1B | GRCh38.p7 | 15:68282112 | AGGGGGAGGTGTCAT[A/G]TGACCATGAAACATT | 10116 |
rs55722829 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | FEM1B | GRCh38.p7 | 15:68282024 | AAGTCACATGAGTGG[A/G]AATGAAAGAAGATCC | 10116 |
rs55941639 | snp | A/G | 0.368324 | 0.220226 | utr-variant-5-prime, upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68277828 | GGAGCGTTCCGCATC[A/G]CCCCGGGGGCCCCTA | 10116 |
rs57074540 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FEM1B | GRCh38.p7 | 15:68289528 | AGTGAGGTCTTGGTC[A/G]GTGGGAGTGAATACA | 10116 |
rs57128886 | snp | A/G | 0.113685 | 0.209567 | intron-variant | FEM1B | GRCh38.p7 | 15:68287937 | CTCCCAGGTTCAAGC[A/G]ATTCTCTTGCCTCAG | 10116 |
rs58268546 | in-del | -/CACA | 0.5 | 0 | intron-variant | FEM1B | GRCh38.p7 | 15:68286495 | ACACACACACACACA[-/CACA]TATACCACACAACCT | 10116 |
rs58402939 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | FEM1B | GRCh38.p7 | 15:68279447 | TTTTTGGGTATTTGA[C/T]CAGAATTGTCAGGTT | 10116 |
rs58984440 | in-del | -/AG | 0.112631 | 0.208878 | intron-variant | FEM1B | GRCh38.p7 | 15:68281806 | ATTTTTAGTAGAGAC[-/AG]GGTTTCACCGTGTTA | 10116 |
rs59231560 | snp | A/G | 0.093417 | 0.194889 | upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68277461 | CCCTTCCCTAACCCC[A/G]GCTCAGGGGCAGAAG | 10116 |
rs59705963 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | FEM1B | GRCh38.p7 | 15:68284542 | GTATATCATATCTAG[G/T]AAAGTACATGAATCT | 10116 |
rs60111545 | in-del | -/T | | | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68292649 | TAGCTTTTTTTTTTT[-/T]CTTTAATGAAAAGCA | 10116 |
rs60432847 | in-del | -/A | | | intron-variant | FEM1B | GRCh38.p7 | 15:68283532 | AAAAAAAAAAAAAAA[-/A]GGTAGTATGCAGGAG | 10116 |
rs60647108 | snp | A/C | 0.0482946 | 0.147699 | intron-variant | FEM1B | GRCh38.p7 | 15:68280580 | GCTGTGTTTTAAAGA[A/C]TAGTAGTAGGACATG | 10116 |
rs60705177 | snp | A/G | 0.0991586 | 0.199366 | downstream-variant-500B | FEM1B | GRCh38.p7 | 15:68296231 | TTTCTATATGTATAG[A/G]TTTTTAAAACAACTT | 10116 |
rs62003787 | snp | C/T | 0.5 | 0 | intron-variant | FEM1B | GRCh38.p7 | 15:68279964 | AACTCCTTGCATTCC[C/T]GCACCTAGAGAAGGA | 10116 |
rs66989829 | snp | G/T | 0.272241 | 0.249009 | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68292880 | GAGGGGACAGAAGGG[G/T]GGACTATCCCCCAAG | 10116 |
rs67342571 | snp | A/G | 0.368938 | 0.219895 | intron-variant | FEM1B | GRCh38.p7 | 15:68281419 | TCTTAGCTTCATCCC[A/G]TGTAATTATGGGTTT | 10116 |
rs71455588 | in-del | -/C | 0.5 | 0 | intron-variant | FEM1B | GRCh38.p7 | 15:68285792 | CTTCTTAGCCCCCCC[-/C]GCAGTGCTGGGATTA | 10116 |
rs71455589 | in-del | -/T | 0.5 | 0 | intron-variant | FEM1B | GRCh38.p7 | 15:68287852 | TTTTTTTTTTTTTTT[-/T]GAGATGAAGTTTTGC | 10116 |
rs71726193 | in-del | -/CA | | | intron-variant | FEM1B | GRCh38.p7 | 15:68286475 | TCGACCTCTTGGACT[-/CA]CACACACACACACAC | 10116 |
rs72038688 | in-del | -/TAACA | | | intron-variant | FEM1B | GRCh38.p7 | 15:68286797 | ATGACAATAAAAACA[-/TAACA]AAAAAATAACAAAAG | 10116 |
rs72741150 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FEM1B | GRCh38.p7 | 15:68279472 | CAGGTTTGACATTAT[C/T]CTCTTTTCTATGCTG | 10116 |
rs72741151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1B | GRCh38.p7 | 15:68281309 | GCTTCATAATTTTTG[A/G]CCAAATTGTTCACTA | 10116 |
rs72741152 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FEM1B | GRCh38.p7 | 15:68282514 | TTTCAGATTGAACCA[A/G]GTAATAGATGAGCTC | 10116 |
rs73427899 | snp | A/T | 0.0726307 | 0.176182 | upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68276204 | GCTACCAGTAGAATC[A/T]TACCTTCAGCCCTTA | 10116 |
rs74019863 | snp | C/T | 0.0185938 | 0.0946107 | upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68276635 | TTGCCTTCCAGAGTT[C/T]ATTCTCCATACAGCA | 10116 |
rs74019864 | snp | C/T | 0.0217236 | 0.101931 | upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68276927 | ACCGTCTGTTCTTGT[C/T]ACTTGTCATAGAGGT | 10116 |
rs74019865 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FEM1B | GRCh38.p7 | 15:68279271 | TATATTGGCTACTAA[A/G]ATGGCATTGGACCTG | 10116 |
rs74019866 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FEM1B | GRCh38.p7 | 15:68279934 | TTTCCTTACTGGCTT[C/T]CGTGTCTTCTCTGTA | 10116 |
rs74019867 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FEM1B | GRCh38.p7 | 15:68280013 | TGAACCTCCAGTACC[A/G]TTCCACCTGTATAGG | 10116 |
rs74019868 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FEM1B | GRCh38.p7 | 15:68280031 | CCACCTGTATAGGCA[C/T]ATGAAGTCATTGAGA | 10116 |
rs74019869 | snp | C/T | 0.113685 | 0.209567 | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68292113 | CCCCTTTTCCCTTTT[C/T]CTCCTGTATCTTTTA | 10116 |
rs74019870 | snp | A/G | 0.113334 | 0.209338 | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68292187 | CTAATAAGGTATTTT[A/G]CTTATGACAGATGAA | 10116 |
rs74019871 | snp | G/T | 0.113334 | 0.209338 | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68293541 | TGAAATGCTGACAGG[G/T]TGGAGAACGAATTTG | 10116 |
rs74019872 | snp | C/T | 0.0539704 | 0.155153 | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68294252 | CTAGTAGCCCACAGC[C/T]CAATCACGTTAAGGT | 10116 |
rs74370426 | snp | G/T | 0.112983 | 0.209108 | intron-variant | FEM1B | GRCh38.p7 | 15:68283533 | AAAAAAAAAAAAAAA[G/T]GTAGTATGCAGGAGG | 10116 |
rs74483643 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | FEM1B | GRCh38.p7 | 15:68288888 | GAACATATTTGTTTA[C/T]TAGAGTCCCCTTTGT | 10116 |
rs74521321 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-5-prime, upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68278200 | CCGCCTTCCTCCCTG[C/T]GCGGGCTGGGTCGCG | 10116 |
rs75191224 | snp | C/T | 0.107341 | 0.205301 | intron-variant | FEM1B | GRCh38.p7 | 15:68285071 | ATACAGCTTCTGTCA[C/T]CACAGATTAGTTTTG | 10116 |
rs75471612 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | FEM1B | GRCh38.p7 | 15:68285020 | TAAGTTGCCCAGTTT[C/T]GGGTATGCCTTTATC | 10116 |
rs75545657 | snp | C/T | 0 | 0 | intron-variant | FEM1B | GRCh38.p7 | 15:68285704 | GTCTTTTTTTTTTTT[C/T]CTTAAATTGAGTAGA | 10116 |
rs75571734 | snp | A/G | 0.0283406 | 0.115616 | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68293457 | ATATGTACATATTCA[A/G]ACATCAAAATTTAAT | 10116 |
rs75959834 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant, utr-variant-5-prime | FEM1B | GRCh38.p7 | 15:68278987 | AGGTGGCTGCCTTTC[C/T]AGGTTTTACTTTTAG | 10116 |
rs76552257 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | FEM1B | GRCh38.p7 | 15:68287688 | ATTTATTTCTCATAT[G/T]TCTGGAAGCTGGAAT | 10116 |
rs77020709 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68292367 | AAATTTTTCAACCAC[A/T]AAATGTCACTTATTC | 10116 |
rs77026141 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FEM1B | GRCh38.p7 | 15:68285897 | TTAATGAAATCCAAT[A/G]AATACTTTCTTTTTC | 10116 |
rs77594247 | snp | A/C | | | missense | FEM1B | GRCh38.p7 | 15:68290481 | GCCCTGCACCTCAGA[A/C]AAAAAGGTAACAGGA | 10116 |
rs77747303 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68277528 | TCCTTAGCCCATCAG[C/T]TTAGCGCCCTCACTC | 10116 |
rs77832887 | snp | C/T | 0.5 | 0 | intron-variant | FEM1B | GRCh38.p7 | 15:68285705 | TCTTTTTTTTTTTTT[C/T]TTAAATTGAGTAGAG | 10116 |
rs78230835 | snp | A/C | 0.0119091 | 0.0762411 | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68295023 | TGCCCAAATCTTTAG[A/C]TGGGCTGGGTTATAC | 10116 |
rs78238174 | snp | A/G | 0.0562307 | 0.157967 | upstream-variant-2KB | FEM1B | GRCh38.p7 | 15:68277604 | AGGAGGAGGTTCCAG[A/G]AGTCAAGGACATTGA | 10116 |
rs78511923 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | FEM1B | GRCh38.p7 | 15:68288621 | TAGCACATATCAGAT[G/T]TTTAGTAAGTAAGTG | 10116 |
rs78587299 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68292649 | GTAGCTTTTTTTTTT[C/T]CTTTAATGAAAAGCA | 10116 |
rs79213461 | in-del | -/TGTTT | | | utr-variant-3-prime | FEM1B | GRCh38.p7 | 15:68291517 | GGAACAGATATAAAA[-/TGTTT]TGTTTATGTAACAAG | 10116 |