SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs339524 | snp | G/T | 0.362104 | 0.223456 | upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40190213 | TTTTTTGTTTGTTTG[G/T]TTTTTGTTGTTTTTT | 4294 |
rs339525 | snp | G/T | 0.361894 | 0.223562 | upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40190606 | ATTTTTAAAACTGCC[G/T]TTCATTTTTGCTTTG | 4294 |
rs339526 | snp | C/T | 0.362104 | 0.223456 | upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40191154 | TGCTAATCGCGTCCG[C/T]TGCAGTCCAACCCAT | 4294 |
rs892117 | snp | C/T | 0.483126 | 0.0902898 | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40205426 | TGTCTTTTCTTAATA[C/T]GCAAAAAAGGCTCCC | 4294 |
rs1046744 | snp | C/T | | | synonymous-codon, nc-transcript-variant | MAP3K10 | GRCh38.p7 | 19:40192421 | GGCCGCCCGGCTGGA[C/T]CCTGAGAAGGACCCG | 4294 |
rs1129156 | snp | C/T | 0.379956 | 0.213568 | synonymous-codon, nc-transcript-variant | MAP3K10 | GRCh38.p7 | 19:40213169 | CATCGCCCCTGGCTT[C/T]GCCAGCCTCAATGAG | 4294 |
rs2356229 | snp | C/T | 0.371785 | 0.218331 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40201383 | atttttcagtagaga[C/T]ggggtttcaccatat | 4294 |
rs3746005 | snp | A/G | 0.326591 | 0.237979 | synonymous-codon, nc-transcript-variant | MAP3K10 | GRCh38.p7 | 19:40214172 | CTGCCCCAGCGCCCC[A/G]TCCGATGGCGTCCGC | 4294 |
rs3746006 | snp | A/G | 0.440143 | 0.162313 | intron-variant, nc-transcript-variant | MAP3K10 | GRCh38.p7 | 19:40213503 | CTCTGCAACCGGAGA[A/G]GGCCATCACTCCGCT | 4294 |
rs3746007 | snp | A/G | 0.00329041 | 0.0404275 | synonymous-codon, nc-transcript-variant | MAP3K10 | GRCh38.p7 | 19:40192211 | GCTGGGGAGCTGCCC[A/G]GTCCACCAGCCCTCG | 4294 |
rs3760917 | snp | A/G | 0.0115144 | 0.0749975 | upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40190571 | AACCAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 4294 |
rs4530264 | snp | A/T | 0.363568 | 0.222716 | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40196529 | TTTATTTATTTATTT[A/T]TTTCATTGAGATGGA | 4294 |
rs4803318 | snp | C/G | 0.199873 | 0.244923 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40206466 | TTATAGTCCAAGCTA[C/G]TGGGGAGGCTGAGGT | 4294 |
rs4803319 | snp | G/T | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40208370 | ttttttttttttttt[G/T]tatttttagtagaga | 4294 |
rs7251116 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40205064 | CAGGCTGAGTCCCCA[C/G]AGCATGACCACTGAC | 4294 |
rs7252471 | snp | A/G | 0.436265 | 0.166749 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40207505 | CTTTTTGGGGCTAAG[A/G]CGGGCAGATCACCTG | 4294 |
rs7257636 | snp | G/T | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40208371 | ttttttttttttttg[G/T]atttttagtagagac | 4294 |
rs7258548 | snp | A/G | 0.363568 | 0.222716 | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40196646 | ACCAAAGCCTCTCAA[A/G]TAGCTGGGACTCCAG | 4294 |
rs7259191 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40211992 | ggcctcccaaagtgc[G/T]gggattccaggcaag | 4294 |
rs8106744 | snp | C/G | 0.362313 | 0.223351 | downstream-variant-500B | MAP3K10, TTC9B | GRCh38.p7 | 19:40215970 | TGGAACATTCCCCCC[C/G]ACCCCACACACCCTC | 4294 |
rs8107448 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40193811 | AAGCAAAGGCATCAG[C/T]AGTGGAGAAGGCCAG | 4294 |
rs8111356 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40194827 | gatttctccctcccc[C/T]agctatggaatttat | 4294 |
rs9749056 | snp | A/C | 0.363776 | 0.222609 | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40197405 | atctcagctcactgc[A/C]acctccacctcccag | 4294 |
rs10402740 | snp | C/G | 0.32885 | 0.23724 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40195274 | ATAAAGATTTTGAAG[C/G]GGGACTGACTTAGGC | 4294 |
rs10423675 | snp | A/G | 0.499977 | 0.00339449 | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40196631 | tcaagtgatcctctc[A/G]ccaaagcctctcaaa | 4294 |
rs10627537 | in-del | -/TT | 0 | 0 | downstream-variant-500B | MAP3K10, TTC9B | GRCh38.p7 | 19:40215611 | TTTTTTTTTTTTTTT[-/TT]GGAGACAGAGTCTTG | 4294 |
rs11406570 | in-del | -/G | 0.363985 | 0.222503 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40194764 | TTAAGTGCCTACTCT[-/G]TACTAGGCACTGCCT | 4294 |
rs11667239 | snp | C/T | | | upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40189691 | ctccctcctcggcct[C/T]tgaaagtgctgggat | 4294 |
rs11671554 | snp | A/T | 0 | 0 | upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40189800 | TCTTGTTAATTTTAG[A/T]GCACCGTTTTGAAGA | 4294 |
rs12971806 | snp | A/C | 0.282369 | 0.247896 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40202115 | GCACGATCTCAGCTC[A/C]CTGCAAGCTCCGCCT | 4294 |
rs12974705 | snp | A/C | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40211656 | tcctgcattattttg[A/C]tgaggataatggctt | 4294 |
rs12979064 | snp | C/G | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40208487 | agacatgagccaccg[C/G]gcccagccCCCATAC | 4294 |
rs12979204 | snp | A/G | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40208382 | tttgtatttttagta[A/G]agacagggtttcacc | 4294 |
rs12979206 | snp | A/G | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40208384 | tgtatttttagtaga[A/G]acagggtttcaccgt | 4294 |
rs12980366 | snp | C/T | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40208349 | gctctttctttcttt[C/T]ttttttttttttttt | 4294 |
rs12980568 | snp | G/T | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40208414 | tgttagccaggatgg[G/T]ctcaatctcctgacc | 4294 |
rs12985458 | snp | G/T | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40198836 | actttgggaggccga[G/T]gtgggcggatcactt | 4294 |
rs12985476 | snp | G/T | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40198859 | gatcacttgaggtca[G/T]gagtttgagaccagc | 4294 |
rs13343617 | snp | A/G | 0.00999975 | 0.0699991 | missense, nc-transcript-variant | MAP3K10 | GRCh38.p7 | 19:40213535 | AGTTCGCGGAGGCAG[A/G]GGATGGAGGCAGCAG | 4294 |
rs13346024 | snp | A/G | 0.00560754 | 0.0526529 | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40205303 | AAGGAGAAGGTGAAG[A/G]CAGGGGGCAAGGTGG | 4294 |
rs28567855 | snp | A/C | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40210999 | CTAGGCGTCCTTTGG[A/C]CCAGTCAAGTTGACG | 4294 |
rs28648489 | snp | G/T | 0 | 0 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40214474 | ACCAGCATGACCATC[G/T]CCAATTCTTACACAG | 4294 |
rs33947268 | in-del | -/G | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40194765 | TAAGTGCCTACTCTT[-/G]ACTAGGCACTGCCTC | 4294 |
rs34769287 | in-del | -/C | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40199885 | TTTGGAGGCCGGGTG[-/C]CGGTGGCTCACGCCT | 4294 |
rs34886198 | snp | A/G/T | 0.0781949 | 0.181616 | synonymous-codon, nc-transcript-variant | MAP3K10 | GRCh38.p7 | 19:40213590 | CCCGTCCTACCTCTC[A/G/T]GTGCCACTGCCTGCC | 4294 |
rs34894858 | snp | A/G | 0.48378 | 0.0885831 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40210745 | AGAACCTGAACACCA[A/G]TGTCCAGTGTCTCAG | 4294 |
rs35370477 | in-del | -/T | 0.625 | 0.125 | upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40190223 | GTTTGTTTTTTGTTG[-/T]TTTTTTTTTTGTTGT | 4294 |
rs35601972 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40199453 | AGCAATCTGAGAAAT[A/G]ATACTTCATCTGAGT | 4294 |
rs35902806 | in-del | -/T | | | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40204834 | TTGGGCCAGGCCCAG[-/T]AGCTCTCAGGACAAC | 4294 |
rs36045799 | in-del | -/T | 0 | 0 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40201512 | TTTTTTTTTTTTTTT[-/T]AACAGGGTCTTGCTC | 4294 |
rs36102209 | snp | A/C | 0.00317592 | 0.0397225 | missense, nc-transcript-variant | MAP3K10 | GRCh38.p7 | 19:40192534 | CCTGCCTCAACCCCC[A/C]ACACCTCTGCCTAGT | 4294 |
rs55708899 | snp | C/G | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40199010 | GAGGCAGAGATTGCA[C/G]TGGGCTGGGATTGGC | 4294 |
rs55987909 | snp | A/G | 0.000140459 | 0.00837914 | synonymous-codon, nc-transcript-variant | MAP3K10 | GRCh38.p7 | 19:40192328 | CTTCCACGAGCTGCA[A/G]CTAGAGGAGATCATC | 4294 |
rs56200572 | snp | C/T | 0.00133983 | 0.025848 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K10 | GRCh38.p7 | 19:40204551 | GATCGACGCCTTGGC[C/T]GTGGCGTATGGCGTG | 4294 |
rs56379332 | snp | G/T | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40194829 | TTTCTCCCTCCCCCA[G/T]CTATGGAATTTATAT | 4294 |
rs57263119 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40193523 | GTGTCAACAAGTATT[A/G]ATTGAGCACCTATTA | 4294 |
rs57661190 | snp | G/T | | | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40204812 | ATCCCCCACATCCCA[G/T]CCCTTGTTTGGGCCA | 4294 |
rs57856272 | snp | C/T | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40195339 | CATGAGATGTTCCCT[C/T]TGTCACAGGGTTTCG | 4294 |
rs58675277 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40195246 | GATTTGAAGCAGGGA[A/G]TGACATGATTACATA | 4294 |
rs58833500 | snp | C/T | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40195395 | AAGAAGGGAAAACTT[C/T]TGCAGAGGTGGAGTT | 4294 |
rs59999853 | snp | A/G | 0.20111 | 0.245173 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40213330 | GGTGGCCCCTGGGGC[A/G]TGGGGGGTCATTTCC | 4294 |
rs60546899 | snp | A/G | | | downstream-variant-500B | MAP3K10, TTC9B | GRCh38.p7 | 19:40215627 | TTTTTTTTTTTTGGA[A/G]ACAGAGTCTTGCTCT | 4294 |
rs60568017 | snp | A/G | 0.337614 | 0.234145 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40200455 | CCATTTACTGTTCCC[A/G]TCAATTCCCAGCTGA | 4294 |
rs61289931 | in-del | -/TTTT | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40195508 | TTTTTTTTTTTTTTT[-/TTTT]GAGACAGAGTCATCT | 4294 |
rs61540617 | in-del | -/TA | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40208690 | ATATATATATATATA[-/TA]CAGTTTAAAAATTAG | 4294 |
rs62106659 | snp | C/T | 0.0622301 | 0.165053 | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40197040 | GCTACCCCCAAAACT[C/T]GGCATCTTAAAACAG | 4294 |
rs62107560 | snp | G/T | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40201224 | GTCGCCCAGGCCGGA[G/T]TACAGCGGCGCGATC | 4294 |
rs62107561 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40203488 | AGGGACCACAGCACA[G/T]TGACGCACGCTCTGG | 4294 |
rs62107562 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40208444 | CTCGTGATCCGCCTG[C/T]CTCGGCCTCCCAAAG | 4294 |
rs62107563 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40209634 | TGGCCAGGCTGGTAT[C/T]GAACTCCTGACCTCA | 4294 |
rs67106164 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40197841 | CCTTGGCTGTTGTTT[C/T]TTTTTTTTGAGACGA | 4294 |
rs67322193 | snp | C/T | 0.481242 | 0.0950111 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40210005 | AGGCGCGGTGGCTCA[C/T]GCCTGTAATTCCAGC | 4294 |
rs67393920 | snp | A/C | 0.0744748 | 0.178019 | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40196881 | TTCATGAGTCAATTC[A/C]TATAGAGAGCTTAGC | 4294 |
rs68037210 | snp | C/T | 0.077417 | 0.180873 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40198992 | AGAATCACTTGAGGC[C/T]GGGAGGCAGAGATTG | 4294 |
rs71171548 | in-del | -/T | 0 | 0 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40200636 | TTTTTTTTTTTTTTT[-/T]GGGACAGAATCTCAC | 4294 |
rs71171549 | in-del | -/T | 0 | 0 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40207909 | AAAATTTTTTTTTTT[-/T]CTGAGATGGGGTCTT | 4294 |
rs71171550 | in-del | -/TA | 0.255224 | 0.249945 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40208673 | TGAGAACTCATCCTT[-/TA]TATATATATATATAT | 4294 |
rs71981575 | in-del | -/A | 0.5 | 0 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40203335 | CAGAGACTTTGTCTC[-/A]AAAAAAAAAAAGGAT | 4294 |
rs72544837 | in-del | -/G | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40194763 | CTTAAGTGCCTACTC[-/G]TTACTAGGCACTGCC | 4294 |
rs73042673 | snp | A/C | 0.410905 | 0.191336 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40195363 | GGTTTCGATACAAAC[A/C]GGAGAGGTGGGGACC | 4294 |
rs73042675 | snp | A/G | 0.410737 | 0.191478 | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40196853 | AATAAAAAAGGGCTC[A/G]GGGTGGGGGTCATTC | 4294 |
rs73042681 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40198989 | AGGAGAATCACTTGA[C/G]GCCGGGAGGCAGAGA | 4294 |
rs73042686 | snp | A/T | 0.0737376 | 0.17729 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40207898 | AAATTTTCATTAAAA[A/T]TTTTTTTTTTTCTGA | 4294 |
rs73933215 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40197052 | ACTCGGCATCTTAAA[A/C]CAGCCATTGTGTATT | 4294 |
rs73933217 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40212587 | AGTTGGCAGGGAACC[A/G]CTCATGGCCTTCAGT | 4294 |
rs74915410 | in-del | -/AA | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40206415 | ACCAAAAAAAAAAAA[-/AA]TTTTTTTTAATTAGC | 4294 |
rs74966166 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40206588 | CTCTAAAGGGAAGAA[G/T]AAGAAAAAAAGAAAA | 4294 |
rs75018626 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40200512 | TAATGGGTATGGGAC[C/T]GAGACAGATCAGACA | 4294 |
rs75429865 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40202809 | TTGAGGATACTTCCT[A/G]GAAGCTAGTTGCCTA | 4294 |
rs75598675 | snp | C/T | | | intron-variant | MAP3K10 | GRCh38.p7 | 19:40196093 | CTGTTACGAGCCCCA[C/T]TTCATAGAGGAGAAG | 4294 |
rs75813080 | snp | A/C/G | 0.0298908 | 0.118541 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40195639 | GGCAGGGCTACAGGC[A/C/G]TGCGCCACCAAGCCT | 4294 |
rs76108009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40198226 | GAGGGGCTCATGGAT[A/G]TTCCAGGCCAGGAAA | 4294 |
rs76454854 | snp | A/C | 0.5 | 0 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40210702 | TGAGACTCAGTCTCA[A/C]AAAAAAAAAAAATTG | 4294 |
rs76456430 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40203740 | GCTTTATAAATGTTA[A/G]ATAATGTTAACTGGT | 4294 |
rs76498412 | snp | G/T | 0.5 | 0 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40209425 | TTTTTTCTTTTTTTT[G/T]GGAGACAGACAGAGT | 4294 |
rs76623654 | snp | C/G | | | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40203746 | TAAATGTTAAATAAT[C/G]TTAACTGGTTTTTAG | 4294 |
rs76799045 | snp | C/G/T | 0.0150606 | 0.0854603 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40195467 | ACACTGAAGCCCGCC[C/G/T]GGCCTTTTTTTTTTT | 4294 |
rs77126152 | snp | A/C | 0.5 | 0 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40210700 | AGTGAGACTCAGTCT[A/C]AAAAAAAAAAAAAAT | 4294 |
rs77253253 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K10 | GRCh38.p7 | 19:40203741 | CTTTATAAATGTTAA[A/G]TAATGTTAACTGGTT | 4294 |
rs77259888 | snp | C/T | 0.5 | 0 | intron-variant | MAP3K10 | GRCh38.p7 | 19:40211317 | TCTGGATTTTCCTTT[C/T]TTTTTTTTTTTTTTT | 4294 |