SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11138 | snp | G/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | MAP3K5 | GRCh38.p7 | 6:136557296 | ATGCGTAATTTCAAT[G/T]ACTGTATAAAGTTTA | 4217 |
rs11503 | snp | C/T | 0 | 0 | utr-variant-3-prime | MAP3K5 | GRCh38.p7 | 6:136557194 | ATTTTGTAACTTAAG[C/T]TTCTGACCTGTCGTA | 4217 |
rs720065 | snp | C/G | 0.145305 | 0.227022 | intron-variant, upstream-variant-2KB | MAP3K5, LOC101928429 | GRCh38.p7 | 6:136783098 | CAGGCTGGTCTCAAA[C/G]TCCTGGACTCAAGCG | 4217 |
rs720344 | snp | C/G | 0.440884 | 0.161442 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136727304 | TTTGAAAAGCATATA[C/G]TGTCTGACACATAGT | 4217 |
rs720345 | snp | C/T | 0.441158 | 0.161117 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136727123 | GGAAGATAATTTTCA[C/T]CTGTTTATTTTACTA | 4217 |
rs742305 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136616960 | tgagctcaagtgatc[C/T]gccagcctcagcctc | 4217 |
rs760862 | snp | C/T | 0.376394 | 0.215696 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136588526 | TAGTTTTTCTTCTTC[C/T]GCTAGAATGTCAACT | 4217 |
rs760863 | snp | A/G | 0.384401 | 0.210799 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136588578 | TGTTCAGTTCGCCAC[A/G]GCATCCCCAGCACAT | 4217 |
rs877192 | snp | A/C | 0.255224 | 0.249945 | intron-variant, upstream-variant-2KB | MAP3K5, LOC101928461 | GRCh38.p7 | 6:136628596 | GGCTGCTAAAGTTTT[A/C]ATTTCCCCTAGGAAT | 4217 |
rs877193 | snp | C/T | 0.249886 | 0.25 | intron-variant, upstream-variant-2KB | MAP3K5, LOC101928461 | GRCh38.p7 | 6:136628646 | TTTTTTAAAAGATTA[C/T]GTATTAGATACAGAT | 4217 |
rs911179 | snp | C/T | 0.422315 | 0.181128 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136740945 | GTGAAAAAAATTCAC[C/T]ATCTTAATGTGACCC | 4217 |
rs911180 | snp | A/G | 0.499793 | 0.0101816 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136713413 | TCTAAGGAATTATGT[A/G]TAGACTGGGTAAAAT | 4217 |
rs911181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136713404 | TTATGTATAGACTGG[A/G]TAAAATATGCCCTTG | 4217 |
rs911182 | snp | A/G | 0.460365 | 0.13508 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136713326 | TGTTTTGAATCTCTT[A/G]TTACCATTTTGTCTA | 4217 |
rs911185 | snp | A/G | 0.499902 | 0.00698814 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136712568 | CACTTGAATAATGTG[A/G]CCCAATTAGGTGTTG | 4217 |
rs932589 | snp | A/G | 0.497933 | 0.032082 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136762000 | GGTTGGTGAACAGAC[A/G]CTCTACTCATTTTAA | 4217 |
rs958293 | snp | A/G | 0.457271 | 0.139781 | intron-variant, nc-transcript-variant | MAP3K5, LOC101928461 | GRCh38.p7 | 6:136637095 | AAAGCATAGTTACTC[A/G]CTATCAGGTAAGTAA | 4217 |
rs1009709 | snp | C/T | 0.48491 | 0.0855403 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136696611 | AGAAACCAGATGTCA[C/T]TTAAATTTTACTATT | 4217 |
rs1009710 | snp | A/G | 0.484701 | 0.0861117 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136696765 | AAAGTTATTTCTGTA[A/G]GTAATCAATTACATA | 4217 |
rs1009711 | snp | A/G | 0.485118 | 0.0849685 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136699498 | GTCAGGCCCTTGTAC[A/G]TTGCATTGCAATTTC | 4217 |
rs1011969 | snp | A/C | 0.425586 | 0.17796 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136658102 | GGAAAATTCTTTAAA[A/C]AGCCATGAGGGCCTA | 4217 |
rs1022690 | snp | A/G | 0.499853 | 0.008585 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136764158 | TTGGAAACATCTACC[A/G]TGGTCTGAACATTCT | 4217 |
rs1028565 | snp | C/T | 0.450105 | 0.149859 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136720227 | GTTCTGAGTTTCAGT[C/T]ATGGTTGTAGCGGAG | 4217 |
rs1028566 | snp | C/G | 0.497473 | 0.0354532 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136719157 | acaggatctcgctct[C/G]tcacccaggctggaa | 4217 |
rs1168074 | snp | C/T | | | upstream-variant-2KB | MAP3K5 | GRCh38.p7 | 6:136794224 | aacactttgggaggc[C/T]gaggcgggcagatca | 4217 |
rs1168075 | snp | A/T | | | upstream-variant-2KB | MAP3K5 | GRCh38.p7 | 6:136794254 | acttgaggtcaggag[A/T]tcaagaccagcctgg | 4217 |
rs1168076 | snp | G/T | | | upstream-variant-2KB | MAP3K5 | GRCh38.p7 | 6:136794264 | aggagttcaagacca[G/T]cctggccaacatggt | 4217 |
rs1321477 | snp | C/T | 0.447162 | 0.153712 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136720695 | GAGGAAATAAGGAAA[C/T]GATAGGGATTTTCTC | 4217 |
rs1474988 | snp | C/T | 0.463881 | 0.12944 | upstream-variant-2KB | MAP3K5 | GRCh38.p7 | 6:136793115 | GGAACACTGGAAATG[C/T]TTCAGGGGCGGACTC | 4217 |
rs1570053 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136780011 | GAGAGACAGGCATAG[A/G]GCCTGCTGAGAATGA | 4217 |
rs1570054 | snp | C/T | 0.467234 | 0.12373 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136780588 | TAATGTGGCGCTTCC[C/T]GTGAAGAATGCACTT | 4217 |
rs1570055 | snp | C/T | 0.437683 | 0.165152 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136738565 | AGATCATCACCACAG[C/T]AACAGACAGTATTTG | 4217 |
rs1570056 | snp | C/T | 0.49999 | 0.00219646 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136738789 | GGAACAGACGGCTGA[C/T]GGCCTAAGGAACCTG | 4217 |
rs1581713 | snp | C/T | 0.440884 | 0.161442 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136725342 | gaggagcatctcagc[C/T]gtccaacatctttgt | 4217 |
rs1804706 | snp | C/T | 1.65192e-05 | 0.00287391 | synonymous-codon | MAP3K5 | GRCh38.p7 | 6:136601848 | GCTTGTTGATGAGTT[C/T]TTAAAAGTTTCAAGC | 4217 |
rs1819155 | snp | A/G | 0.49998 | 0.00319482 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136744651 | GCACACCCCTCACCA[A/G]CACCTACACCAGGGA | 4217 |
rs1923120 | snp | C/G | 0.494936 | 0.050064 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136790040 | TGGAATCCTGCATTG[C/G]CCACTTACTCCCTAT | 4217 |
rs1997703 | snp | C/T | 0.44651 | 0.154543 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136648715 | TAGAAACTATAGCAC[C/T]GGGACTGGTGATTTC | 4217 |
rs2002623 | snp | G/T | 0.459347 | 0.136653 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136717060 | CAGCTCACTGCAACC[G/T]CCGCCTCCAGAGTAG | 4217 |
rs2014569 | snp | A/G | 0.498109 | 0.0306926 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136712758 | CACCCCCGTAATTCA[A/G]TTATCTCCCACCAGG | 4217 |
rs2014570 | snp | C/T | 0.459801 | 0.135955 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136712749 | AATTCAGTTATCTCC[C/T]ACCAGGTCCCTCCCA | 4217 |
rs2016706 | snp | C/T | | | intron-variant | MAP3K5 | GRCh38.p7 | 6:136726426 | GGTGAAACCCTGTCT[C/T]TACTAAAAATACAAA | 4217 |
rs2064205 | snp | C/T | 0.384017 | 0.211044 | intron-variant | MAP3K5, LOC101928461 | GRCh38.p7 | 6:136636526 | CTGGAGAAGTGTCAT[C/T]CTTCAGACATTGAAG | 4217 |
rs2076259 | snp | C/T | 0.182933 | 0.240836 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136613938 | TTCCTGGGTGGCTAT[C/T]CTCAAGCTTTGCACT | 4217 |
rs2076260 | snp | C/T | 0.396864 | 0.202314 | synonymous-codon | MAP3K5 | GRCh38.p7 | 6:136656430 | AAAATGCTTATATAT[C/T]AAAATTGTCTCTACA | 4217 |
rs2076261 | snp | C/T | 0.00500667 | 0.0497822 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136656478 | GAGAAGGAAAAGATA[C/T]AAAACATGTAACAGA | 4217 |
rs2076262 | snp | C/T | 0.268724 | 0.249298 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136592079 | CACTACAGGTTCCTC[C/T]TGCCTTTCACATCAT | 4217 |
rs2143020 | snp | A/G | 0 | 0 | intron-variant | MAP3K5, LOC101928461 | GRCh38.p7 | 6:136631444 | TGAGGCCAATCATCA[A/G]AAAAGAAAACAGTAA | 4217 |
rs2143021 | snp | A/G | 0.490727 | 0.0674567 | intron-variant | MAP3K5, LOC101928461 | GRCh38.p7 | 6:136631574 | CTGGAGTGCAGTGGC[A/G]CAATCCTAGCTCACT | 4217 |
rs2179347 | snp | C/T | 0.455858 | 0.141853 | intron-variant | MAP3K5, LOC101928461 | GRCh38.p7 | 6:136636437 | CCCAATGGACTAAGT[C/T]ACTTGGATTCAGAGT | 4217 |
rs2206193 | snp | G/T | 0 | 0 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136601526 | TACACTTGAACCTTA[G/T]TATCCACAATGTTAG | 4217 |
rs2224378 | snp | A/T | 0.440746 | 0.161604 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136725010 | ttacctttcccagaa[A/T]gtcatataaatggaa | 4217 |
rs2237262 | snp | C/G | 0.369346 | 0.219673 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136566196 | AGAGAAGGAAAAGGA[C/G]TTGTGTCTAGGCTGC | 4217 |
rs2237263 | snp | A/G | 0.239902 | 0.249796 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136574328 | TGAAGCTCCTCGTAC[A/G]TACACAATGCTGTTC | 4217 |
rs2237264 | snp | A/G | 0.165527 | 0.235296 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136598840 | GTCATTGTTTCAATT[A/G]ACATGAGGCAGGCCA | 4217 |
rs2237265 | snp | C/T | 0.453575 | 0.145111 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136616493 | CATTTTTAGTAGAGA[C/T]GGAGTTTCACCATGT | 4217 |
rs2237266 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136616954 | AACTCCTGAGCTCAA[A/G]TGATCCGCCAGCCTC | 4217 |
rs2237268 | snp | C/T | 0.370365 | 0.219117 | intron-variant | MAP3K5, LOC101928461 | GRCh38.p7 | 6:136631792 | CAGATTGAATCTCTT[C/T]TACTTGGACACCTGG | 4217 |
rs2237269 | snp | C/G | 0.399611 | 0.200291 | intron-variant | MAP3K5, LOC101928461 | GRCh38.p7 | 6:136645481 | TTGATAATCCGTGAG[C/G]TAGGCCAAGGGTGCC | 4217 |
rs2237270 | snp | C/T | 0.407502 | 0.194147 | intron-variant | MAP3K5, LOC101928461 | GRCh38.p7 | 6:136645603 | CTTTCATTGTACACA[C/T]GCAGACTTTCTTCAA | 4217 |
rs2237271 | snp | A/C | 0.42357 | 0.179927 | intron-variant | MAP3K5, LOC101928461 | GRCh38.p7 | 6:136647403 | CATGCCTAGGCCACG[A/C]AGCATGCAAGAGCTA | 4217 |
rs2272887 | snp | A/G | 0.416708 | 0.186302 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136658996 | CCAGTGGGTTGGTCA[A/G]TGTGCAGGAGAGGCT | 4217 |
rs2273557 | snp | C/T | 0.497359 | 0.0362457 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136696268 | AAAACATTAGAAACA[C/T]ACAGTTACCATGTTG | 4217 |
rs2277100 | snp | A/G | 0.0754868 | 0.179012 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136600981 | TTTATCACACCAGAC[A/G]CCAGGTCTCAGCTCA | 4217 |
rs2282857 | snp | A/G | 0.267636 | 0.249377 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136594435 | CTATTTGGGGGGAAC[A/G]GACTTTAGAACAGAA | 4217 |
rs2327740 | snp | A/G | 0.19334 | 0.243495 | downstream-variant-500B | MAP3K5 | GRCh38.p7 | 6:136556729 | CAATCATGGCTCACC[A/G]CAATCTCGACCTCCC | 4217 |
rs2327741 | snp | A/G | 0.195837 | 0.244062 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136559848 | AGCTTTTACTTTTAA[A/G]CCAAATAAAAAGGGT | 4217 |
rs2327742 | snp | A/G | 0.388398 | 0.208197 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136563030 | AGCACATACACCCCT[A/G]ATTTTATTGAAATAC | 4217 |
rs2327743 | snp | C/T | 0.453939 | 0.144598 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136588104 | CCTAAAATCAAGCAT[C/T]TTAAAGGTCCACAGG | 4217 |
rs2327744 | snp | G/T | 0 | 0 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136589089 | AGCAAAGAAGCACAG[G/T]GAGTTTCTCAAGGCA | 4217 |
rs2327756 | snp | A/G | 0.285257 | 0.247501 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136725072 | tctttgacttagcaa[A/G]atgcatgtgagattc | 4217 |
rs2327757 | snp | A/G | 0.498982 | 0.0225409 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136727699 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 4217 |
rs2327758 | snp | C/T | 0.441158 | 0.161117 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136727923 | GCAGAGATAGCACCA[C/T]TGCACTCCAGCCTGG | 4217 |
rs2327759 | snp | G/T | 0.488485 | 0.0749998 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136732254 | acatggtgaaatacc[G/T]tctctaccaaaaata | 4217 |
rs2876335 | snp | A/G | | | intron-variant | MAP3K5 | GRCh38.p7 | 6:136681744 | acatggtgaaactcc[A/G]tctctactaaaaata | 4217 |
rs2876345 | snp | C/G | 0.440609 | 0.161766 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136727776 | CCATCCTGGCTAACA[C/G]GGTGAAACCCCGTCT | 4217 |
rs2876346 | snp | A/G | 0.499996 | 0.00139776 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136727828 | TTAGCCGGGCGTGGT[A/G]GCAGGTGCCTGTAGT | 4217 |
rs2876347 | snp | A/G | 0.49999 | 0.00219646 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136743367 | aggcaggagaatggc[A/G]tgaacccgggaggcg | 4217 |
rs3040779 | in-del | -/TTTTTT | | | intron-variant | MAP3K5 | GRCh38.p7 | 6:136562857 | ttttttttttttttt[-/TTTTTT]gtagagacagagtct | 4217 |
rs3040783 | in-del | -/TG | | | intron-variant | MAP3K5 | GRCh38.p7 | 6:136669894 | TCAGGGTGTGTGTGT[-/TG]GTGTGTGTGTGTGTG | 4217 |
rs3041756 | snp | A/C/G/T | 0.5 | 0 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136761308 | aaaaaaaaaaaaaaa[A/C/G/T]GAACAGTCAGCCAGG | 4217 |
rs3734552 | snp | A/G | 0.446771 | 0.154211 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136791495 | GGTGGGTGGATCCAT[A/G]GGTCTATCGCACAAG | 4217 |
rs3757165 | snp | C/T | 0.48995 | 0.0701706 | upstream-variant-2KB | MAP3K5 | GRCh38.p7 | 6:136794881 | ATTTTCAACAACTTG[C/T]CAAACCTCCAAAACC | 4217 |
rs3757166 | snp | C/T | 0.480853 | 0.0959518 | upstream-variant-2KB | MAP3K5 | GRCh38.p7 | 6:136794985 | TGTGGAAAACTAAAA[C/T]GCCTAAATGCTCAAG | 4217 |
rs3765258 | snp | A/G | 0.108511 | 0.206112 | synonymous-codon | MAP3K5 | GRCh38.p7 | 6:136622925 | TGCGTAGACTATCCC[A/G]TAAGTGCCTTTTCCT | 4217 |
rs3765259 | snp | C/T | 0.495056 | 0.049474 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136669145 | CACCAAACAAGGAGA[C/T]ATAATAAGTTTCTTT | 4217 |
rs3831521 | in-del | -/CAC | 0.177503 | 0.239258 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136566419 | CAGGAGTCCAAAAAA[-/CAC]CACCACTCAGGACTG | 4217 |
rs3903659 | snp | A/G | 0.497881 | 0.0324789 | upstream-variant-2KB | MAP3K5 | GRCh38.p7 | 6:136794674 | TCAATGTGACATTAG[A/G]TTTTTCTAAAGGTGT | 4217 |
rs4243449 | snp | A/G | 0.499839 | 0.00898417 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136701584 | TCCCACAGCACATCC[A/G]CCCAATTTAATCCTT | 4217 |
rs4286798 | snp | C/G | 0.460589 | 0.13473 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136706882 | CCTGGTGCCGTGGCT[C/G]ACGCCTGTAAATCTC | 4217 |
rs4351280 | snp | A/G | 0.386694 | 0.20932 | downstream-variant-500B | MAP3K5 | GRCh38.p7 | 6:136556908 | CTGAGGAACAACCTG[A/G]ATGTCAGTTGTCTGA | 4217 |
rs4363056 | snp | C/T | 0.3752 | 0.216391 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136676481 | TACATCTTAATGTTA[C/T]TGGAGTTCACGACTT | 4217 |
rs4524621 | snp | C/G | 0.445724 | 0.155538 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136790526 | TAAAAATACCAGAAC[C/G]AGAAAGTCCTAGTTT | 4217 |
rs4598089 | snp | G/T | 0.420574 | 0.182769 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136727724 | CCAGCACTTTGGGAG[G/T]CCAAGGCGGGCGGAC | 4217 |
rs4631311 | snp | A/G | 0.360632 | 0.224189 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136572065 | TTGCAGGGGCTAAAC[A/G]TATTAGGTCTTCAAA | 4217 |
rs4895468 | snp | A/G | 0.460027 | 0.135605 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136711437 | TGGGAGGCAGAGGCA[A/G]GCAGATCACTGGAGC | 4217 |
rs4896212 | snp | C/T | 0.494358 | 0.0528145 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136697542 | AATAAATATCTTACA[C/T]ATCTGGCATTATTAA | 4217 |
rs4896213 | snp | A/G | 0.48 | 0.0979796 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136707569 | ACTTGGGGGGGGGGG[A/G]AACCCCTTGAACGTA | 4217 |
rs4896214 | snp | A/G | 0.460589 | 0.13473 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136707762 | aagaagtatcagcac[A/G]tattggggcaccatt | 4217 |
rs4896216 | snp | G/T | 0.499713 | 0.0119774 | intron-variant | MAP3K5 | GRCh38.p7 | 6:136716865 | CAATGCTAAAGAAAA[G/T]AAAAAGAATTGGCCA | 4217 |