SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs14429 | snp | A/T | 0 | 0 | missense | MAP2K5 | GRCh38.p7 | 15:67806716 | GGGTGTGCCGGGCGC[A/T]GGAGGAGAGGCGGAG | 5607 |
rs737226 | snp | A/G | 0.423726 | 0.179776 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548435 | ACACCAATAACTGGA[A/G]TATTACAAAGCTTAC | 5607 |
rs737227 | snp | G/T | 0.239037 | 0.24976 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548571 | TCTCTGTGCCTCACT[G/T]TCCTCATGTGTAATA | 5607 |
rs745212 | snp | A/G | 0.472147 | 0.114677 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767841 | CTGTGTAATGCCTGC[A/G]TGTAATCCTTTGAAC | 5607 |
rs745213 | snp | G/T | 0.450231 | 0.149691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768051 | TTGTAGCCTCTTCGG[G/T]GTTTTTTGTTGTCTG | 5607 |
rs752682 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707427 | AACAAAGTGCATTCT[A/G]TAACATAGTCAACAC | 5607 |
rs868036 | snp | A/T | 0.499203 | 0.0199521 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762675 | TCTTTTTCTCCTAAA[A/T]GTGTTTTGGAAGTTC | 5607 |
rs868037 | snp | C/T | 0.499218 | 0.0197529 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762658 | TGTTTTGGAAGTTCT[C/T]CAGTATTGGGATAAA | 5607 |
rs884202 | snp | A/G | 0.499218 | 0.0197529 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762050 | TTTAGACCAGCCTGA[A/G]CAGGAGACTTCCCAC | 5607 |
rs938874 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660471 | CATAGTCTGATTGTG[A/T]TCCCAGTATCCTTGG | 5607 |
rs938875 | snp | A/G | 0.496416 | 0.0421803 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660584 | GCCATTGCCAAGTCA[A/G]AAGCAACAGAATCAG | 5607 |
rs938876 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707418 | AATCTGAGGAACAAA[A/G]TGCATTCTGTAACAT | 5607 |
rs938877 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707577 | GGAGAGTGGGGCACA[C/G]AGAGCTGAGGAGAGC | 5607 |
rs938878 | snp | A/G | 0.496348 | 0.0425753 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701028 | GGGCAGGATCAAAAA[A/G]GAGGTTAAACACACT | 5607 |
rs938879 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700992 | CATTTGCCCACTGAA[A/C]TATCAAAACAAATGC | 5607 |
rs938880 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700974 | TCAAAACAAATGCAA[A/G]CTGTAAGCTGATAAT | 5607 |
rs951656 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632778 | ATTACATTAGAATTG[C/T]TTATACCTTTTAGTA | 5607 |
rs997295 | snp | G/T | 0.496483 | 0.0417852 | intron-variant, downstream-variant-500B | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67724005 | CTCATAAGCAAATGA[G/T]TTTTTTCCTAGTTTT | 5607 |
rs1026731 | snp | A/G | 0.5 | 0.000399361 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802680 | TAACATGCTTTCCGC[A/G]TGAAGGACGGAGGCC | 5607 |
rs1026732 | snp | A/G | 0.5 | 0.000399361 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802747 | TCTTGACAAGCATCT[A/G]TATTGGTGCCTGGGT | 5607 |
rs1026733 | snp | A/G | 0.5 | 0.000399361 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802784 | GAGCTGCACCATGCC[A/G]CGCTTCCATTGTTCC | 5607 |
rs1054650 | snp | C/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762190 | GGCTGCAGAGAAAGA[C/G]GACAATAACGGGTTT | 5607 |
rs1054651 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762195 | CAGAGAAAGAGGACA[A/G]TAACGGGTTTTACTT | 5607 |
rs1054652 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762199 | GAAAGAGGACAATAA[C/G/T]GGGTTTTACTTTTGT | 5607 |
rs1063934 | snp | G/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793558 | ATACTAAGCTTGTTA[G/T]AATCAAGTCTAAAAT | 5607 |
rs1471460 | snp | A/G | 0.499998 | 0.000998401 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796961 | accggcacacattgt[A/G]tctgttcacatggcg | 5607 |
rs1806482 | snp | A/G | 0.296873 | 0.245566 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547759 | ACTGCGCCCATCCCG[A/G]TTTTCTTTTGAAACC | 5607 |
rs1814895 | snp | A/G | 0.323671 | 0.238899 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612048 | GATAAAATTTCCAGG[A/G]AGTCATGTGTTGAAC | 5607 |
rs1878699 | snp | C/T | 0.318896 | 0.240319 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608545 | CCATCAGTTCTTCCT[C/T]AGCCCCCCAGATCTG | 5607 |
rs1878700 | snp | A/G | 0.317692 | 0.240661 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608130 | TACACCCTACAACAC[A/G]GAAGTGCGCTAATGT | 5607 |
rs1878701 | snp | A/C | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660802 | TCTAATTAGTCAGTA[A/C]AAATTTGAACACAGG | 5607 |
rs1878702 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665036 | TTGCTTCACATACTG[C/G]AAAGAAAAACTTTAT | 5607 |
rs1984442 | snp | A/G | 0.496714 | 0.0404017 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713674 | ATCTCGGCTCACTGC[A/G]ACCTCTGCCTCCTGG | 5607 |
rs1984443 | snp | C/T | 0.440471 | 0.161928 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713522 | TCTCAAACTCCCGAC[C/T]TCAGGTGATCAACCC | 5607 |
rs1996482 | snp | C/T | 0.323434 | 0.238972 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603233 | TTAAACAGTAACTCC[C/T]CCATCACTCTGTTAA | 5607 |
rs2045960 | snp | A/G | 0.472052 | 0.11486 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799741 | GCCCACCCACCCAAT[A/G]TTGCCACTCCCTCCC | 5607 |
rs2045961 | snp | A/G | 0.364401 | 0.222289 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799933 | TTGCTGTCACTCCAC[A/G]CAGAGTGGGGGGCAG | 5607 |
rs2045962 | snp | A/G | 0.164873 | 0.23506 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799947 | CACAGAGTGGGGGGC[A/G]GTGGGGGGGATTGTT | 5607 |
rs2127162 | snp | A/C | 0.441977 | 0.16014 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798486 | TGCCCCATCCAACAC[A/C]GTACAACACTGGTCC | 5607 |
rs2127163 | snp | C/T | 0.417521 | 0.185571 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798504 | ACAACACTGGTCCTG[C/T]GGCTGCTCTGTAAGT | 5607 |
rs2241420 | snp | A/G | 0.482083 | 0.0929373 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790478 | TCTGAGGGCACTGCC[A/G]TCTTGTCTGTAGGCT | 5607 |
rs2241421 | snp | A/G | 0.499996 | 0.00139776 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790487 | ACTGCCGTCTTGTCT[A/G]TAGGCTGTGCACAAG | 5607 |
rs2241422 | snp | A/C | 0.473451 | 0.112115 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790734 | AAACAAACAAACAAA[A/C]AAAAAAAAACCTGTG | 5607 |
rs2241423 | snp | A/G | 0.482008 | 0.0931261 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794500 | GTAATTTTCAATCCT[A/G]TAGAAAACTAGACTA | 5607 |
rs2278076 | snp | A/G | 0.433963 | 0.169285 | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807262 | TGCTAGCTCCTCGCA[A/G]TTGTGCTGAGGCCCA | 5607 |
rs2288098 | snp | A/C | 0.311123 | 0.242413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693173 | GGGCTTCATTCACAT[A/C]TTGAGCCATCTGACT | 5607 |
rs2414962 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547717 | CCACTTCGGCCCCCC[A/G]AAGTGCTGGGATTAT | 5607 |
rs2414963 | snp | A/G | 0.0513262 | 0.151752 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548914 | ACAGATTTATTTTTG[A/G]AAAAAAAAAAAAGCA | 5607 |
rs2414966 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613000 | TTAGCTGATAGTTAA[A/G]AGAGGAGTTATTTAC | 5607 |
rs2414967 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613001 | TAGCTGATAGTTAAA[A/T]GAGGAGTTATTTACA | 5607 |
rs2414968 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613002 | AGCTGATAGTTAAAA[G/T]AGGAGTTATTTACAG | 5607 |
rs2414969 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621986 | atcaggagttcgaga[C/T]cagcctggacaacat | 5607 |
rs2414970 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622260 | gaagcaatggagcaa[A/G]ccaggtatatattgg | 5607 |
rs2414971 | snp | A/T | 0.0410537 | 0.137264 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598963 | TTACTTAGAGAAATG[A/T]TCTAAGGGAATTAGC | 5607 |
rs2414972 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665464 | TTGGGGAATGGAACA[A/G]CATACACATTAGATG | 5607 |
rs2414973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666735 | CAGCCCAATTCCTAC[A/G]GAGAGTAGCCTGCTA | 5607 |
rs2414974 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678359 | TTGCTTTATAGGGGG[A/G]AAAAGTTGAAGAGAA | 5607 |
rs2414975 | snp | A/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679611 | GTTTATCAGGCCTAG[A/T]GCATATCAGTTCTAA | 5607 |
rs2414976 | snp | C/T | 0.0356815 | 0.128715 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680650 | TTCTGCTCACTGATA[C/T]TTTTCTAATAATCTT | 5607 |
rs2414977 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684085 | agtcctagaaaggca[A/G]gaacatgcagagaaa | 5607 |
rs2459919 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577307 | taataaagttaaatg[C/T]cttcctgaaggctac | 5607 |
rs2583571 | snp | C/G | 0.0130921 | 0.0798413 | | | GRCh38.p7 | 15:67564405 | GAGACCCTAATCTTA[C/G]TCAACAGTTAGGTTG | 5607 |
rs2583573 | snp | A/C | 0.00398564 | 0.0444627 | | | GRCh38.p7 | 15:67559590 | CAGCAGATGGTAAAC[A/C]AATATTATGAAGCAA | 5607 |
rs2583575 | snp | G/T | 0.00438332 | 0.0466095 | | | GRCh38.p7 | 15:67573556 | agatttgtgggcggg[G/T]acacaaatccaaacc | 5607 |
rs2583580 | snp | A/G | 0.00517822 | 0.0506191 | | | GRCh38.p7 | 15:67570970 | TTCTTCCATACATCT[A/G]TAACAGGAGAGTTTC | 5607 |
rs2583581 | snp | C/T | 0.0360663 | 0.129354 | | | GRCh38.p7 | 15:67569132 | TGATGCTATTAAATA[C/T]TCAACTTCTAAATGG | 5607 |
rs2583585 | snp | C/T | 0.319856 | 0.240042 | | | GRCh38.p7 | 15:67567381 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 5607 |
rs2583586 | snp | A/G | 0.00438332 | 0.0466095 | | | GRCh38.p7 | 15:67566760 | TCTATTTAAATTACT[A/G]ATAAAAATGTACACT | 5607 |
rs2583587 | snp | A/G | 0.44768 | 0.153045 | | | GRCh38.p7 | 15:67545070 | TGAAAATCAACCTAT[A/G]TAAGTGAGGCACAGA | 5607 |
rs2583588 | snp | C/T | 0.0146672 | 0.084371 | | | GRCh38.p7 | 15:67544798 | CTCAAAATGAAGTTA[C/T]AGAAATCAAATTTTG | 5607 |
rs2583589 | snp | G/T | 0.336879 | 0.245063 | | | GRCh38.p7 | 15:67544302 | TCCCTTACTTTTACC[G/T]TCTCTGAAACTGGAC | 5607 |
rs2583590 | snp | G/T | 0.305934 | 0.243663 | | | GRCh38.p7 | 15:67543915 | TCAAAATAAATTAAT[G/T]AAACAGTGTGCTCAA | 5607 |
rs2583591 | snp | G/T | 0.0107246 | 0.0724382 | | | GRCh38.p7 | 15:67543768 | GGAAAAAACCTCTCT[G/T]CTAGATTCAGCAGTT | 5607 |
rs2583592 | snp | A/G | | | | | GRCh38.p7 | 15:67548168 | GCTATTCCTAAGTAG[A/G]AAGGAACCTAAATTA | 5607 |
rs2583593 | snp | A/G | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 15:67548174 | CCTAAGTAGAAAGGA[A/G]CCTAAATTAATTTGC | 5607 |
rs2589976 | snp | C/T | 0.0333695 | 0.124785 | | | GRCh38.p7 | 15:67577873 | AGCTGGGATTACAGG[C/T]ACCCACCACTGGCCC | 5607 |
rs2589977 | snp | A/G | 0.314301 | 0.241589 | | | GRCh38.p7 | 15:67587332 | CATTACAGGGCCTAC[A/G]AGGCCCCGCATGATA | 5607 |
rs2589978 | snp | C/T | 0.314544 | 0.241524 | | | GRCh38.p7 | 15:67577231 | TATAGGGTTACTGGC[C/T]GGGCACGGTGGCTCA | 5607 |
rs2589979 | snp | C/T | 0.0158469 | 0.0875917 | | | GRCh38.p7 | 15:67577146 | agatcgagaccatcc[C/T]ggctaacaaggtgaa | 5607 |
rs2589980 | snp | C/T | 0.00199481 | 0.0315187 | | | GRCh38.p7 | 15:67587022 | TCTCTTTGGTCAATA[C/T]GTAGCTAGGTTATCT | 5607 |
rs2589981 | snp | A/G | 0.00478085 | 0.0486577 | | | GRCh38.p7 | 15:67573071 | actaaacatacccag[A/G]ttcaggaatgtcctg | 5607 |
rs2589982 | snp | G/T | 0.318656 | 0.240388 | | | GRCh38.p7 | 15:67566259 | TGAACCCAGGAGGCG[G/T]AGGTTGCAGTGAGCC | 5607 |
rs2589983 | snp | G/T | 0.319376 | 0.240181 | | | GRCh38.p7 | 15:67561477 | ATACACTGGTCACTT[G/T]CAGTAATGAAGAAGG | 5607 |
rs2589984 | snp | A/G | 0.00398564 | 0.0444627 | | | GRCh38.p7 | 15:67559414 | CCAATAGAGAGGAGA[A/G]GCAGCCTCAGGTAAG | 5607 |
rs2589985 | snp | C/T | 0.454544 | 0.143743 | | | GRCh38.p7 | 15:67552752 | AAACAGAGCTAATAA[C/T]GTCCTTTTAAGTACT | 5607 |
rs2589986 | snp | C/T | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 15:67552084 | ATTCATCCACCCCCT[C/T]CCGCCCCCACCAACC | 5607 |
rs2589987 | snp | C/G | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 15:67545381 | ttctGTCCACAGAAC[C/G]ATAATTGCATGCATC | 5607 |
rs2678675 | snp | C/T | 0.314787 | 0.241459 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572791 | tgcaaactcacctct[C/T]gggttcaagtgattc | 5607 |
rs2678676 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574353 | AAGGTGGGTGGATCA[C/T]GTGAGGTCAGGAGTT | 5607 |
rs2678677 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576686 | TAACAGGAGAAAACA[C/T]ATTTTATAATTGCTG | 5607 |
rs2678678 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577092 | AGGCGCCCGCCACCG[C/T]GCCCGGCTAATTTTT | 5607 |
rs2678679 | snp | C/T | 0.321769 | 0.239477 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582687 | ATTAGCCGGGCGTGG[C/T]GCACACTCCTGTTGT | 5607 |
rs2678680 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587492 | ATCCTGCCCTCCTTT[A/G]ATGTTTGACTTCCTA | 5607 |
rs2899726 | snp | A/G | 0.458545 | 0.137872 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614616 | GAGATCAGAATGACT[A/G]TAGTTTCCTTGATCT | 5607 |
rs2899727 | snp | A/G | 0.321769 | 0.239477 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619941 | taggcatggtggttc[A/G]ctcctgtagactcaa | 5607 |
rs2899728 | snp | A/T | 0.32153 | 0.239548 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622414 | ACCAGGGCCCAGATG[A/T]TGAAATCCTTATAAA | 5607 |
rs2899729 | snp | A/G | 0.288906 | 0.246954 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652850 | tgtctctatgtgact[A/G]ctctaggtacctcat | 5607 |
rs3083901 | in-del | -/AA | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664354 | aaaaaaaaaaaaaaa[-/AA]gctaggcatgatggt | 5607 |
rs3223318 | microsatellite | (CA)17/19/20/21/22/23 | 0.744666 | 0.121441 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547079 | caaaaaagangaaaa[(CA)17/19/20/21/22/23]aGATTTCTGTCTAAA | 5607 |
rs3743353 | snp | C/T | 0.299158 | 0.245119 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543032 | ACGGCGGCAGAGACC[C/T]TCACCATAGCGTTCG | 5607 |