SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1140054 | snp | A/G | | | utr-variant-3-prime | CDC40 | GRCh38.p7 | 6:110231487 | cctgggcgacagagc[A/G]agactccatctcaaa | 51362 |
rs4339500 | snp | A/G | 0.395635 | 0.2032 | intron-variant, upstream-variant-2KB | CDC40, WASF1 | GRCh38.p7 | 6:110190611 | TAATGAAATTTAGTA[A/G]GCAGTTGGATATGTG | 51362 |
rs4343947 | snp | A/G | 0.362104 | 0.223456 | intron-variant | CDC40 | GRCh38.p7 | 6:110199363 | CACTTTGGGAGGCAG[A/G]GGCGGGCGGATACGA | 51362 |
rs4421235 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC40 | GRCh38.p7 | 6:110211123 | GTTGACTCTTTTGGT[A/G]TATTAATAGTGCCCC | 51362 |
rs4509164 | snp | A/G | 0.424659 | 0.17887 | intron-variant | CDC40 | GRCh38.p7 | 6:110198954 | CAAGAACAGCTGAGA[A/G]ACCTATCTTGAGTAA | 51362 |
rs4947058 | snp | A/G | 0.354665 | 0.227036 | intron-variant | CDC40 | GRCh38.p7 | 6:110216482 | GAACAAAATGTCTCC[A/G]TCAGATAGAGTGGAT | 51362 |
rs6908812 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | CDC40 | GRCh38.p7 | 6:110214174 | TTTGGAGTAAAAACC[C/T]CCATTTTACTTAACT | 51362 |
rs6913554 | snp | A/G | 0.368324 | 0.220226 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | WASF1, CDC40 | GRCh38.p7 | 6:110179521 | GGCTCGCGGGACTCC[A/G]CCTAGAGCCCCCAGG | 51362 |
rs6917918 | snp | C/T | 0.376592 | 0.215579 | intron-variant | CDC40 | GRCh38.p7 | 6:110220593 | gggactacaggcgcc[C/T]gccaccacgcccggc | 51362 |
rs6918022 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CDC40 | GRCh38.p7 | 6:110220498 | tgtgccacccaggct[A/G]cagtggcgcaatctc | 51362 |
rs6918148 | snp | C/T | 0.395087 | 0.203592 | intron-variant | CDC40 | GRCh38.p7 | 6:110211602 | TAATTGCTGTATATA[C/T]ACTATGTCATTTAAT | 51362 |
rs6918158 | snp | C/T | 0.084728 | 0.187577 | intron-variant | CDC40 | GRCh38.p7 | 6:110211609 | TGTATATATACTATG[C/T]CATTTAATTCTCACA | 51362 |
rs6938106 | snp | A/G | 0.425586 | 0.17796 | intron-variant | CDC40 | GRCh38.p7 | 6:110218686 | ttcaaaggtatttat[A/G]taattggtatggcta | 51362 |
rs6938139 | snp | A/G | 0.377977 | 0.21476 | intron-variant | CDC40 | GRCh38.p7 | 6:110218755 | actactATTTTGCAG[A/G]TTCTTTTAAAaatca | 51362 |
rs6938653 | snp | C/T | 0.353587 | 0.22753 | intron-variant | CDC40 | GRCh38.p7 | 6:110218895 | gatctagaacatttg[C/T]ggcactcagtaaagg | 51362 |
rs7740923 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110185304 | ctggagtgcagtggc[A/G]ggatctcggctcact | 51362 |
rs7740924 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110185305 | tggagtgcagtggcg[G/T]gatctcggctcactg | 51362 |
rs7744828 | snp | A/T | 0.396909 | 0.202282 | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110182328 | CTTGCTAGCTTACGA[A/T]CTTGAGAGGTATATA | 51362 |
rs7756891 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | CDC40 | GRCh38.p7 | 6:110229581 | AAGCCAAAAAGTAAT[A/T]ATGAAAGTGTTAGAG | 51362 |
rs7761436 | snp | A/G | 0.498754 | 0.0249289 | upstream-variant-2KB, intron-variant | WASF1, CDC40 | GRCh38.p7 | 6:110181628 | CCTAACTTCCTATCA[A/G]AACAAAACTTTCCAA | 51362 |
rs7763743 | snp | C/T | 0.140581 | 0.224783 | intron-variant | CDC40 | GRCh38.p7 | 6:110207080 | agcactttgggaggc[C/T]aaggcggtggatcat | 51362 |
rs7766850 | snp | C/G | 0.423413 | 0.180077 | intron-variant | CDC40 | GRCh38.p7 | 6:110223192 | tgggctcaagcgatc[C/G]tcctgccttagactc | 51362 |
rs7774748 | snp | A/T | 0 | 0 | intron-variant | CDC40 | GRCh38.p7 | 6:110229600 | AAAGTGTTAGAGCCT[A/T]CTGTGATAGAATAGA | 51362 |
rs7775143 | snp | C/T | 0.257176 | 0.249897 | intron-variant | CDC40 | GRCh38.p7 | 6:110202139 | CAGGAAAGAGAATAG[C/T]GAAAAATTCATTATG | 51362 |
rs7775237 | snp | C/T | 0.12932 | 0.218944 | intron-variant | CDC40 | GRCh38.p7 | 6:110220670 | caggatggtctcgat[C/T]tcctgaccttatgat | 51362 |
rs9384735 | snp | A/G | 0.362941 | 0.223034 | intron-variant | CDC40 | GRCh38.p7 | 6:110220692 | CCTTATGATCCGCCC[A/G]CCTTGGCCTCCCAAA | 51362 |
rs9386883 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | CDC40 | GRCh38.p7 | 6:110213474 | AGCTCACTGCAAGCT[C/T]CGCCTCCCGGGTTCA | 51362 |
rs9398232 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | CDC40 | GRCh38.p7 | 6:110225442 | CATTCTTTCATCACT[C/G]ACATGAGGTTTTTTT | 51362 |
rs9400366 | snp | C/T | 0.481473 | 0.0944461 | intron-variant | CDC40 | GRCh38.p7 | 6:110220472 | TTTTTTTTTTTGAGA[C/T]GGATTCTTGCTGTGC | 51362 |
rs9400367 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC40 | GRCh38.p7 | 6:110222197 | gaggtcaaggctgcc[A/G]tggtctatgcttgtg | 51362 |
rs9481042 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110188667 | TCAGCCAAACAGATG[C/T]ACCAACCTAAGCTTT | 51362 |
rs9481043 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC40 | GRCh38.p7 | 6:110191903 | ATATAATTTCTTTAC[A/G]ATTTTTAAAATAGAA | 51362 |
rs9481045 | snp | A/G | 0.416218 | 0.186739 | intron-variant | CDC40 | GRCh38.p7 | 6:110222426 | GCTGGGCGTGGTGGC[A/G]GGCGCGTGTAATCCC | 51362 |
rs9481046 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | CDC40 | GRCh38.p7 | 6:110222878 | ATGTTacactgattg[A/C]gctctttctatatgc | 51362 |
rs9481047 | snp | A/C | 0.390453 | 0.208772 | intron-variant | CDC40 | GRCh38.p7 | 6:110227180 | ATCCATTGTCTTTTA[A/C]GTACAAGATAATTTG | 51362 |
rs9487314 | snp | C/G | 0 | 0 | intron-variant | CDC40 | GRCh38.p7 | 6:110203785 | TATTTCTCCTGACTT[C/G]TCAGCCCCTCAGTGG | 51362 |
rs9487315 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | CDC40 | GRCh38.p7 | 6:110220681 | cgatttcctgacctt[A/G]tgatccgcccacctt | 51362 |
rs9487316 | snp | A/G | 0.435694 | 0.167385 | intron-variant | CDC40 | GRCh38.p7 | 6:110220780 | GCGGCAGCAAGAGAG[A/G]GAATGAGAGCCAAGT | 51362 |
rs9487317 | snp | A/G | 0.389152 | 0.207694 | intron-variant | CDC40 | GRCh38.p7 | 6:110223165 | TCATTGCTCACTGCA[A/G]CCTTGAACTCCTGGG | 51362 |
rs9487318 | snp | C/T | 0.390838 | 0.206555 | intron-variant | CDC40 | GRCh38.p7 | 6:110227037 | AGTAATAGTGATTTA[C/T]TGTAAACTCTTTCAG | 51362 |
rs9487319 | snp | A/C | 0.393987 | 0.204372 | intron-variant | CDC40 | GRCh38.p7 | 6:110227417 | TTTTTATGAGAAGAG[A/C]AACCTAACTGAACCT | 51362 |
rs9487320 | snp | A/G | 0.149665 | 0.228982 | utr-variant-3-prime | CDC40 | GRCh38.p7 | 6:110231373 | GGCTTGGTGGCTGGC[A/G]CCTGTAATTCCAGCT | 51362 |
rs11153226 | snp | A/G | 0.425894 | 0.177655 | intron-variant | CDC40 | GRCh38.p7 | 6:110194977 | CTTTTTCCTCGGGTT[A/G]GAGAACCTCACATTA | 51362 |
rs11153227 | snp | A/G | 0.365439 | 0.221752 | intron-variant | CDC40 | GRCh38.p7 | 6:110198564 | ATTTATTTTCTTACT[A/G]TTGAGTTGAGTTCCT | 51362 |
rs11752726 | snp | A/G | 0.140581 | 0.224783 | intron-variant | CDC40 | GRCh38.p7 | 6:110209357 | GCCTTTAGTTGATTG[A/G]AAATATACAATAAAA | 51362 |
rs11753534 | snp | A/T | 0.243347 | 0.249911 | intron-variant | CDC40 | GRCh38.p7 | 6:110225742 | CCATGGTACATTTTT[A/T]ATTTAATTTTTGGTT | 51362 |
rs11754018 | snp | C/T | | | intron-variant | CDC40 | GRCh38.p7 | 6:110204151 | ccctagtagctggga[C/T]tacaggcacccgcca | 51362 |
rs11754051 | snp | A/G | | | intron-variant | CDC40 | GRCh38.p7 | 6:110204163 | ggactacaggcaccc[A/G]ccaccacgcctggct | 51362 |
rs11756892 | snp | C/T | 0.115438 | 0.210697 | intron-variant | CDC40 | GRCh38.p7 | 6:110223545 | CAATTACTAGTGATA[C/T]TGGCCACTTGCTTAG | 51362 |
rs11757055 | snp | C/T | 0.396727 | 0.202413 | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110183477 | ACCCAGGAGGAAAGG[C/T]TGCGTAAGGTACCAG | 51362 |
rs11759054 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC40 | GRCh38.p7 | 6:110227363 | TCCATCAGGGCCTCT[A/G]ACACAAGCAAATGGT | 51362 |
rs12110744 | snp | A/T | 0.367503 | 0.220665 | intron-variant | CDC40 | GRCh38.p7 | 6:110194484 | GTAGCACAGCCAGAG[A/T]TGTCAGTGCTTGTGT | 51362 |
rs12174885 | snp | A/G | 0.0188071 | 0.0951306 | intron-variant | CDC40 | GRCh38.p7 | 6:110221895 | TTTCATTTCCTCTCA[A/G]ATCTTAGGAAATACT | 51362 |
rs12174887 | snp | A/G | 0.00657888 | 0.056975 | intron-variant | CDC40 | GRCh38.p7 | 6:110221958 | TGATGACATTCTTTA[A/G]ATTTTACTGTAACTT | 51362 |
rs12660086 | snp | C/T | | | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110185199 | gtttctgtcacttct[C/T]tctttctctctttca | 51362 |
rs12660087 | snp | A/T | | | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110185206 | tcacttctttctttc[A/T]ctctttcaccctttc | 51362 |
rs12660088 | snp | A/C/T | 0.00557542 | 0.0525036 | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110185208 | acttctttctttctc[A/C/T]ctttcaccctttctt | 51362 |
rs12662099 | snp | A/G | 0.093777 | 0.195178 | intron-variant | CDC40 | GRCh38.p7 | 6:110198999 | GTCCTGCTAAGTAGC[A/G]TTCGCTGCCTTCCTC | 51362 |
rs12662559 | snp | A/C | 0.159951 | 0.233219 | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110187493 | ACCTTTTCCCTCTGC[A/C]ATCTGTTAAGGGCCA | 51362 |
rs12664697 | snp | A/G | 0.159951 | 0.233219 | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110185536 | TCTTAACCCTTTAAA[A/G]ATACAAATACCATCC | 51362 |
rs12665152 | snp | C/G | 0.114738 | 0.210248 | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110187166 | TGTATTTTTAGTAGA[C/G]ACGGGGTTTCACCAT | 51362 |
rs28450902 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CDC40 | GRCh38.p7 | 6:110207800 | GTTGTGGAATCTTGT[A/G]GGGAAAATAATGATA | 51362 |
rs34255523 | in-del | -/T | | | intron-variant | CDC40 | GRCh38.p7 | 6:110216217 | ACAGCTTTGTGACAA[-/T]ACCAGATTTTTGGTA | 51362 |
rs34380939 | in-del | -/G | | | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110188854 | TCCTCACTGGATGGG[-/G]TTCTGTGATGATTAA | 51362 |
rs34403459 | in-del | -/G | | | intron-variant, upstream-variant-2KB | CDC40, WASF1 | GRCh38.p7 | 6:110191163 | GTGGTCAAATTTTGG[-/G]AACAGTGAATGTGGG | 51362 |
rs34428706 | in-del | -/T | | | intron-variant | CDC40 | GRCh38.p7 | 6:110216839 | GCAATATTCATTTTT[-/T]AAGTAAAGTATAATA | 51362 |
rs34508877 | in-del | -/G | | | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110187723 | CAGGAAGAAATGTGG[-/G]AAAAGACTGAAAAGT | 51362 |
rs34592146 | snp | A/G | 0.000412075 | 0.0143481 | synonymous-codon | CDC40 | GRCh38.p7 | 6:110201626 | GATATGAGCTGGTTC[A/G]GCATATCCAGAAAGC | 51362 |
rs34607416 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CDC40, WASF1 | GRCh38.p7 | 6:110190162 | AGTACAGCATTTTTT[-/T]AGGACCACAAACAAA | 51362 |
rs34708220 | in-del | -/T | | | downstream-variant-500B | CDC40 | GRCh38.p7 | 6:110232478 | ACTACACAACATTTT[-/T]AGAGTACATAAATGA | 51362 |
rs34808678 | in-del | -/T | | | intron-variant | CDC40 | GRCh38.p7 | 6:110205484 | AAATAATACTGTTTT[-/T]CTAATCACCTGGGGT | 51362 |
rs34813064 | in-del | -/G | | | intron-variant, upstream-variant-2KB | CDC40, WASF1 | GRCh38.p7 | 6:110190377 | TTAAAGCAGATAAGG[-/G]AAGTATTACAATAGG | 51362 |
rs34987298 | in-del | -/G | | | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110184901 | GACAAATATACAATT[-/G]ACAGTGAGAGATTTT | 51362 |
rs35022176 | in-del | -/A | | | intron-variant | CDC40 | GRCh38.p7 | 6:110207310 | ACAGGGTGAGACCCT[-/A]TCTCAAAAAAAAAAA | 51362 |
rs35052779 | multinucleotide-polymorphism | CAA/TGG | | | intron-variant | CDC40 | GRCh38.p7 | 6:110204174 | ACCCGCCACCACGCC[CAA/TGG]CTAATTTTTGTATTT | 51362 |
rs35139466 | in-del | -/T | | | intron-variant | CDC40 | GRCh38.p7 | 6:110216065 | TGCCTTTGGGATATT[-/T]GAGGTAAAAATGTTC | 51362 |
rs35364703 | in-del | -/C | | | intron-variant | CDC40 | GRCh38.p7 | 6:110229532 | AATTGGGCCTACCTC[-/C]TGATTCAGTCTTAGA | 51362 |
rs35374410 | in-del | -/T | | | intron-variant | CDC40 | GRCh38.p7 | 6:110216814 | ACTTTTAAAAGAGTT[-/T]GAGTGAACTGGCAAT | 51362 |
rs35477743 | in-del | -/T | | | intron-variant | CDC40 | GRCh38.p7 | 6:110218511 | AAAGAGCTAACTTTT[-/T]CAGGGTCACACAGCT | 51362 |
rs35773242 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC40 | GRCh38.p7 | 6:110226419 | TCATATGCAAGTCAC[C/G]TCACCTACTTTTCTG | 51362 |
rs35872442 | in-del | -/G | | | intron-variant | CDC40 | GRCh38.p7 | 6:110219670 | CTTCTCCACTTTCCA[-/G]GAATTATGGTCTTTC | 51362 |
rs35873443 | in-del | -/G | | | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110182270 | ACACACAATGAACAC[-/G]TAATTAAATGCTTGC | 51362 |
rs35998512 | in-del | -/A | | | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110187612 | TGGGAGGAAAAAAAA[-/A]CTATGCCATAAATTG | 51362 |
rs36077644 | in-del | -/G | | | frameshift-variant | CDC40 | GRCh38.p7 | 6:110228832 | TATTGAATTTACAGG[-/G]AAAATGGCTAGCATG | 51362 |
rs36121596 | snp | G/T | 0 | 0 | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110184906 | AATATACAATTACAG[G/T]GAGAGATTTTTATAT | 51362 |
rs41288576 | snp | A/G | 0.160609 | 0.233472 | upstream-variant-2KB, intron-variant | WASF1, CDC40 | GRCh38.p7 | 6:110180019 | TTGGCTAGGGAATGA[A/G]GGAAGATGATAGCCA | 51362 |
rs41288578 | snp | G/T | 0.227334 | 0.24897 | intron-variant | CDC40 | GRCh38.p7 | 6:110229020 | GTATTCAAATATGAT[G/T]ATATAAACTGTTGTT | 51362 |
rs55721034 | snp | C/T | 0.0345262 | 0.126772 | utr-variant-3-prime | CDC40 | GRCh38.p7 | 6:110230341 | TACAGAAAGTGGCTA[C/T]TGACTTTCTATTTGA | 51362 |
rs55827800 | snp | A/G | 0.243347 | 0.249911 | intron-variant | CDC40 | GRCh38.p7 | 6:110223352 | ATCATATGAATGGAT[A/G]GTTAGATGAATGAGG | 51362 |
rs55895216 | in-del | -/T | | | intron-variant | CDC40 | GRCh38.p7 | 6:110204680 | TTTTTTTTTTTTTTT[-/T]GAGACAGGATCTCGC | 51362 |
rs55956228 | snp | A/G | 0.243347 | 0.249911 | intron-variant | CDC40 | GRCh38.p7 | 6:110227227 | ACAATATACTGATGT[A/G]ATTATAGCTTTACAT | 51362 |
rs56000341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110182547 | TCTTCCTCAGCCCCT[A/G]AAGCTAGTCATTCAA | 51362 |
rs56070461 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime | CDC40 | GRCh38.p7 | 6:110230286 | AAATTTGACATAATT[C/T]CATTTGCAACTTCAT | 51362 |
rs56085802 | snp | A/C | 0.0648419 | 0.167978 | intron-variant | CDC40, WASF1 | GRCh38.p7 | 6:110189125 | AGCTCTTCCCCTTCC[A/C]ATTTATTCTATTAGT | 51362 |
rs56092341 | snp | A/T | 0.108048 | 0.20579 | intron-variant | CDC40 | GRCh38.p7 | 6:110213423 | GAGATGGAGTCTTGC[A/T]GTGTTGCCCAGGCTG | 51362 |
rs56715176 | in-del | -/TT | | | intron-variant | CDC40 | GRCh38.p7 | 6:110204679 | TTTTTTTTTTTTTTT[-/TT]GAGACAGGATCTCGC | 51362 |
rs57057428 | snp | A/G | | | upstream-variant-2KB, intron-variant | WASF1, CDC40 | GRCh38.p7 | 6:110181627 | TCCTAACTTCCTATC[A/G]AACAAAACTTTCCAA | 51362 |
rs57068634 | snp | A/C | 0.0618563 | 0.164627 | intron-variant | CDC40 | GRCh38.p7 | 6:110195520 | ATTAGCTCTGTGTAA[A/C]CTTGGACGTTCTTAG | 51362 |
rs57074235 | snp | C/T | | | intron-variant | CDC40 | GRCh38.p7 | 6:110227575 | ATTTAAGTCTGTTTC[C/T]TTAGTAAGTAATGTT | 51362 |
rs57104292 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CDC40 | GRCh38.p7 | 6:110198530 | AAATTCAAGTCCTTT[A/G]CCAATTTTTAATTGA | 51362 |