SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9668 | snp | A/C | 0 | 0 | utr-variant-3-prime | CUL3 | GRCh38.p7 | 2:224474206 | TTCTTGGACTGTACT[A/C]TTCGCATGGACTGGG | 8452 |
rs765409 | snp | A/G | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224533632 | AGATAGTTAGGATGC[A/G]ATTTAAAGACTCACC | 8452 |
rs767146 | snp | C/T | 0.357877 | 0.225527 | intron-variant | CUL3 | GRCh38.p7 | 2:224524167 | GTAGGGCCAAGATTC[C/T]GGAGAAAAGGCAAAC | 8452 |
rs931544 | snp | C/T | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224493523 | GTAAGTTTTCCAACT[C/T]TATCTAAGTCACACA | 8452 |
rs940316 | snp | G/T | 0.356811 | 0.226034 | intron-variant | CUL3 | GRCh38.p7 | 2:224493403 | GAAGGCACAAGAAAT[G/T]TGTCTTTACTCAACA | 8452 |
rs940317 | snp | A/G | 0.346368 | 0.23068 | intron-variant | CUL3 | GRCh38.p7 | 2:224493401 | AGGCACAAGAAATGT[A/G]TCTTTACTCAACACC | 8452 |
rs940318 | snp | C/T | 0.357238 | 0.225832 | intron-variant | CUL3 | GRCh38.p7 | 2:224490773 | TGAACAAAAGGGAGT[C/T]CAGAAGCAAACTAAT | 8452 |
rs1027340 | snp | G/T | 0.498481 | 0.027514 | intron-variant | CUL3 | GRCh38.p7 | 2:224505837 | TGCTGTGCTTAAATG[G/T]GTGCCATGGTCTATT | 8452 |
rs1057404 | snp | A/C | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224510398 | GAGCCATGTTTATCT[A/C]TAGTGGAATCCTTAC | 8452 |
rs1058360 | snp | A/T | 0.340108 | 0.233197 | intron-variant | CUL3 | GRCh38.p7 | 2:224584525 | AGCTAGGCTGGGTAA[A/T]TTTTCAAAGTGTAGC | 8452 |
rs1268948 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | CUL3 | GRCh38.p7 | 2:224561116 | ACTCCAACCCACATT[C/T]TTCATTATTTTCCTG | 8452 |
rs1269800 | snp | A/G | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224487500 | tctctgataaaaaaa[A/G]acaaagaagggcatt | 8452 |
rs1269801 | snp | A/G | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224487506 | ataaaaaaaaacaaa[A/G]aagggcattacataa | 8452 |
rs1466723 | snp | A/G | 0.356811 | 0.226034 | intron-variant | CUL3 | GRCh38.p7 | 2:224483854 | GCCTGTTTTTCAAAA[A/G]CAAATTTCTAGAAAT | 8452 |
rs1466724 | snp | A/C | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224484240 | AACAATTTAACCCCC[A/C]ACAAAAATAGTATAT | 8452 |
rs1494108 | snp | A/T | 0.35894 | 0.225016 | intron-variant | CUL3 | GRCh38.p7 | 2:224576851 | TACACACTTACTCTA[A/T]GGATTACATGTGAAT | 8452 |
rs1494109 | snp | A/G | 0.34101 | 0.232846 | intron-variant | CUL3 | GRCh38.p7 | 2:224577116 | AATATTGGCCTAATC[A/G]TGGCTAAATATTGGT | 8452 |
rs1523917 | snp | G/T | 0.350764 | 0.228794 | intron-variant | CUL3 | GRCh38.p7 | 2:224512890 | CTTGAACAACACAAG[G/T]TTGAACTGCACAGGT | 8452 |
rs1523918 | snp | A/G | 0.498547 | 0.0269177 | intron-variant | CUL3 | GRCh38.p7 | 2:224519711 | TAAGGGTACAGATGC[A/G]TAACCCTTGAGTATT | 8452 |
rs1523919 | snp | A/G | 0.358303 | 0.225323 | intron-variant | CUL3 | GRCh38.p7 | 2:224538898 | TTTAAGTACGATGCA[A/G]TAGTGTGTCCGTGGT | 8452 |
rs1523922 | snp | C/T | 0.357877 | 0.225527 | intron-variant, upstream-variant-2KB | CUL3 | GRCh38.p7 | 2:224560978 | TTGCTATTCTTTCTG[C/T]CTGAAATGTTCTTCC | 8452 |
rs1540823 | snp | C/T | 0.359152 | 0.224913 | intron-variant | CUL3 | GRCh38.p7 | 2:224536182 | ctgaattaacgctag[C/T]aatacacttaaaaca | 8452 |
rs1542786 | snp | A/G | 0.359152 | 0.224913 | intron-variant | CUL3 | GRCh38.p7 | 2:224575873 | CAAGCCTGTCTGATC[A/G]CCACTGTAGATCCAG | 8452 |
rs1542787 | snp | A/G | 0.359152 | 0.224913 | intron-variant | CUL3 | GRCh38.p7 | 2:224575990 | TAGAGGCTAGACATA[A/G]TATCTGTGAGGAATG | 8452 |
rs1542788 | snp | C/T | 0.35894 | 0.225016 | intron-variant | CUL3 | GRCh38.p7 | 2:224576004 | AATATCTGTGAGGAA[C/T]GTATTAACATAGTAT | 8452 |
rs1542789 | snp | A/G | 0.358728 | 0.225118 | intron-variant | CUL3 | GRCh38.p7 | 2:224576091 | AGATGGTCATAGGGA[A/G]AGAGCAGGAGAGTAA | 8452 |
rs1568750 | snp | A/T | 0.416545 | 0.186448 | intron-variant | CUL3 | GRCh38.p7 | 2:224477880 | TAATAATGGTTACCA[A/T]TCATTAAATGCTTTC | 8452 |
rs1632705 | snp | A/C | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224498380 | TGGATAGTGACAAAA[A/C]ACATAAATATAAAAA | 8452 |
rs1690607 | snp | A/C | | | intron-variant | CUL3 | GRCh38.p7 | 2:224496777 | AGGGACACAAAGTGG[A/C]ACTTTCTATTTTTTC | 8452 |
rs1690608 | snp | A/C | | | intron-variant | CUL3 | GRCh38.p7 | 2:224496800 | ATTTTTTCTATAATT[A/C]ACATACGCATATGTT | 8452 |
rs1690610 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CUL3 | GRCh38.p7 | 2:224565397 | gtggcacaggcacaa[A/C/G]agatggaggagggag | 8452 |
rs1690611 | snp | G/T | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224524560 | TATTCACAGAGCATA[G/T]TTCCTCTGGGGTCTG | 8452 |
rs1690612 | snp | C/G | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224524515 | CTGAGGTGTTTGCCA[C/G]GTTGCCTTCTGAATT | 8452 |
rs1690613 | snp | G/T | 0.273806 | 0.248864 | intron-variant | CUL3 | GRCh38.p7 | 2:224524494 | CTTCTGAATTAATGT[G/T]CCTAGAATTCTAACA | 8452 |
rs1690614 | snp | G/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224524431 | TTTGATAGTTTCTGT[G/T]TGGATTCTTGGTGTC | 8452 |
rs1690615 | snp | G/T | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224504867 | GCTCACGACAGCATA[G/T]AAAATCAACTGAAGC | 8452 |
rs1690616 | snp | C/T | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224533126 | CTGTGGTCAACCCTT[C/T]ACACTGCCCAGCAGT | 8452 |
rs1690617 | snp | C/G | | | intron-variant | CUL3 | GRCh38.p7 | 2:224493504 | CTAAGTCACACAGCA[C/G]AAACTGATTGTGGTG | 8452 |
rs1690618 | snp | G/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224493482 | ATTGTGGTGTATATA[G/T]AATGCCATGCCTATG | 8452 |
rs1690619 | snp | C/G | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224542482 | agcagcacgcgccag[C/G]acttctggctttttg | 8452 |
rs1690620 | snp | G/T | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224543018 | AACACACATAATTGT[G/T]TTTAATCATTAATTA | 8452 |
rs1721271 | snp | A/G | 0.0137924 | 0.0818901 | intron-variant | CUL3 | GRCh38.p7 | 2:224493492 | GCACAAACTGATTGT[A/G]GTGTATATATAATGC | 8452 |
rs1721272 | snp | G/T | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224492643 | TTTTTCTTTTCATGT[G/T]TTTTGAATGACTAAA | 8452 |
rs1721274 | snp | C/T | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224498863 | ATTATTGACTTGTAG[C/T]TTCATAAATTAAAAA | 8452 |
rs1721275 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | CUL3 | GRCh38.p7 | 2:224569935 | GGGAAAATACTTGAT[C/T]TTAATTTCAAGCTCC | 8452 |
rs1721276 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | CUL3 | GRCh38.p7 | 2:224569954 | ATTTCAAGCTCCAGT[C/T]TCaaaaaaaaaaaaa | 8452 |
rs1801826 | snp | A/G | | | utr-variant-3-prime | CUL3 | GRCh38.p7 | 2:224473107 | ATTCTTGGATATTTA[A/G]CTATTGTCCTCCAAA | 8452 |
rs1801827 | snp | C/G | | | utr-variant-3-prime | CUL3 | GRCh38.p7 | 2:224473985 | GCTGCGTTTTGTTTT[C/G]TTTACTGTATGAAAA | 8452 |
rs1808013 | snp | C/T | 0.359364 | 0.22481 | intron-variant | CUL3 | GRCh38.p7 | 2:224524314 | AGCTAGGACTTAAGA[C/T]GTCAAGGTTCTGAAG | 8452 |
rs1829920 | snp | A/G | 0.357451 | 0.225731 | intron-variant | CUL3 | GRCh38.p7 | 2:224522603 | GAGGCCGAGGCGGGC[A/G]GATCATGAGGTCAGG | 8452 |
rs1829921 | snp | A/G | 0.356811 | 0.226034 | intron-variant | CUL3 | GRCh38.p7 | 2:224522743 | TGAGGCAGGAGAATG[A/G]TATGAACCCGGGAGG | 8452 |
rs1829922 | snp | A/C | 0.359152 | 0.224913 | intron-variant | CUL3 | GRCh38.p7 | 2:224522835 | accgtctcaaaaaaa[A/C]aaTCCTTCTCAGGGG | 8452 |
rs1851767 | snp | A/G | 0.0425829 | 0.139564 | intron-variant, upstream-variant-2KB | CUL3 | GRCh38.p7 | 2:224570639 | TTTTCTTTTTCCTTG[A/G]CATCAGCTCTTTTTT | 8452 |
rs1880176 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CUL3 | GRCh38.p7 | 2:224549849 | TCTGACTTACATATA[C/T]ACATATATGCGTGCA | 8452 |
rs1963593 | snp | A/G | 0.355954 | 0.226437 | intron-variant | CUL3 | GRCh38.p7 | 2:224505288 | TAGCTGGGCATGGTG[A/G]TGGATGCCTGTAATC | 8452 |
rs1963594 | snp | A/G | 0.34526 | 0.23114 | intron-variant | CUL3 | GRCh38.p7 | 2:224505200 | cagtgagccaagatg[A/G]cgccactgcactcca | 8452 |
rs2047134 | snp | A/C | 0.414905 | 0.187899 | intron-variant | CUL3 | GRCh38.p7 | 2:224482996 | AGTCATTCTCTCTAG[A/C]CAAGTCTTTGAGCAA | 8452 |
rs2047135 | snp | C/G | 0.343701 | 0.231776 | intron-variant | CUL3 | GRCh38.p7 | 2:224562585 | AGAGGCTGAAGTAAG[C/G]CGAGATCGCGCCAGC | 8452 |
rs2068244 | snp | A/G | 0.34437 | 0.231505 | intron-variant | CUL3 | GRCh38.p7 | 2:224575294 | GACCAGGGACATAAA[A/G]GAAACTGCTCAGAGG | 8452 |
rs2068245 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | CUL3 | GRCh38.p7 | 2:224575468 | TAAGAAAGGGGCAAC[C/T]GGTAACATAGGTGGA | 8452 |
rs2070127 | snp | A/G | 0.300979 | 0.244747 | synonymous-codon | CUL3 | GRCh38.p7 | 2:224481929 | TACAGTTAATGATCA[A/G]TTCACATCCAAACTA | 8452 |
rs2131813 | snp | A/G | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224518971 | ACATCAGTCAGAACT[A/G]ATGAATTCTTCAGGA | 8452 |
rs2140508 | snp | A/C | 0.345925 | 0.230864 | intron-variant | CUL3 | GRCh38.p7 | 2:224491122 | ATAATTCATCTGGAC[A/C]AGAAAATGCACAAGA | 8452 |
rs2172658 | snp | A/G | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224492525 | GTTTTTGAAAGAGGT[A/G]TGGATAAGAACTATT | 8452 |
rs2396092 | snp | A/G | 0.357024 | 0.225933 | utr-variant-3-prime | CUL3 | GRCh38.p7 | 2:224470573 | GGAAAACATTTTGTA[A/G]AACTGTAGATTTGAA | 8452 |
rs2396093 | snp | C/T | 0.343477 | 0.231866 | intron-variant | CUL3 | GRCh38.p7 | 2:224485703 | cagaattaaatgttc[C/T]tgcctgctggctctg | 8452 |
rs2396094 | snp | C/T | 0.357238 | 0.225832 | intron-variant | CUL3 | GRCh38.p7 | 2:224485717 | cttgcctgctggctc[C/T]gaagagagcagtgga | 8452 |
rs2396107 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CUL3 | GRCh38.p7 | 2:224554509 | GAGAATtcaagggct[C/T]agactaaagccacat | 8452 |
rs2453180 | snp | A/C | | | intron-variant | CUL3 | GRCh38.p7 | 2:224496853 | AATACACTTCAAAAG[A/C]ACATGATTTTTAGGG | 8452 |
rs2453181 | snp | A/G | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224510267 | GCTTCCTTTTTAAAA[A/G]ACTCTTCAGTTAAAC | 8452 |
rs2453182 | snp | A/G | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224574652 | CTCCAGGCTCCCTGT[A/G]AACGTTTGAAAATAA | 8452 |
rs2453183 | snp | C/G | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224531461 | TAATGAGTTGGTGCA[C/G]AGTTATATTGTATGT | 8452 |
rs2453184 | snp | A/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224493969 | Gaattttttttactt[A/T]tatttatattattat | 8452 |
rs2453185 | snp | C/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224526575 | tttttgaaacggagt[C/T]tccctttgtcgccca | 8452 |
rs2462134 | snp | A/C | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224510331 | ttaaattacatataa[A/C]ttttCAGGGATTTCT | 8452 |
rs2462135 | snp | A/C | | | intron-variant | CUL3 | GRCh38.p7 | 2:224526429 | gtctttaagaaaaat[A/C]caaaaaattagctgg | 8452 |
rs2462136 | snp | C/G | | | intron-variant, upstream-variant-2KB | CUL3 | GRCh38.p7 | 2:224558772 | tccagacgtgagcca[C/G]tgcgcccagccAAGG | 8452 |
rs2642178 | snp | G/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224492494 | AATACATATTTTTGT[G/T]AATGTGCTTTATTTT | 8452 |
rs2710600 | snp | G/T | 0 | 0 | intron-variant | CUL3 | GRCh38.p7 | 2:224492425 | AAATTCTGACATTAA[G/T]AGTGCTATTGTCTGT | 8452 |
rs2710601 | snp | A/C | | | intron-variant | CUL3 | GRCh38.p7 | 2:224492488 | TTATAAAAAATAAAG[A/C]ACATTAACAAAAATA | 8452 |
rs2934606 | snp | A/G | | | intron-variant | CUL3 | GRCh38.p7 | 2:224578851 | AAAGTCCCCCAATGT[A/G]TAATATAAAAAAAAG | 8452 |
rs2934607 | snp | C/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224579137 | GACAAAATAAATACT[C/T]TGTTAATAACAACCG | 8452 |
rs2934608 | snp | C/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224579260 | AGTATAAGTAACACT[C/T]TAATGAATCTGTGTC | 8452 |
rs2934609 | snp | G/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224579273 | CTCTAATGAATCTGT[G/T]TCACTTTGTTTCATA | 8452 |
rs2934610 | snp | A/G | | | intron-variant | CUL3 | GRCh38.p7 | 2:224579593 | TGTGAGTCGCCCTGT[A/G]TGTGCCAGCTAACAA | 8452 |
rs2934616 | snp | G/T | | | intron-variant, upstream-variant-2KB | CUL3 | GRCh38.p7 | 2:224559429 | ctgcactccagccta[G/T]gtgacagagcaagat | 8452 |
rs2934619 | snp | G/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224584436 | CACTGTCACTGCGTC[G/T]GGGGCAGGTTGATGG | 8452 |
rs2934620 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL3 | GRCh38.p7 | 2:224584456 | CAGGTTGATGGCATA[G/T]ACCTTCCTGGGGAGG | 8452 |
rs2934621 | snp | G/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224584515 | TCACCCTATAAGCTA[G/T]GCTGGGTAAATTTTC | 8452 |
rs2934622 | snp | G/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224584809 | TTGCCGGGAAGGCTc[G/T]cgccccgcggccggc | 8452 |
rs2934623 | snp | G/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224584884 | TTCAGCCCGGGCCTC[G/T]CGTGCGGGTCTcggg | 8452 |
rs2934624 | snp | C/G | | | intron-variant | CUL3 | GRCh38.p7 | 2:224584920 | ccccggccccggggT[C/G]CCGGACGCCGAGGAG | 8452 |
rs2934626 | snp | A/G | | | intron-variant | CUL3 | GRCh38.p7 | 2:224526583 | tttttttttttttga[A/G]acggagtctcccttt | 8452 |
rs2949011 | snp | A/G | | | intron-variant | CUL3 | GRCh38.p7 | 2:224526569 | ccagcctgggcgaca[A/G]agggagactccgtct | 8452 |
rs2969781 | snp | A/G | | | intron-variant | CUL3 | GRCh38.p7 | 2:224578869 | ATATAAAAAAAAGGC[A/G]TACCACTTTTTCTAG | 8452 |
rs2969782 | snp | G/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224579113 | CTGAACTGCTATCTA[G/T]AAAGACAAGACAAAA | 8452 |
rs2969783 | snp | C/G | | | intron-variant | CUL3 | GRCh38.p7 | 2:224579375 | TTCCTCTATGTACCA[C/G]TCCAGGTAGTACTAT | 8452 |
rs2969784 | snp | G/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224579537 | TAAGACTCTTCCTGT[G/T]CTTAAGTATATCACA | 8452 |
rs2969785 | snp | G/T | | | intron-variant | CUL3 | GRCh38.p7 | 2:224579597 | AGTCGCCCTGTATGT[G/T]CCAGCTAACAATCAC | 8452 |
rs2969786 | snp | C/G | | | intron-variant | CUL3 | GRCh38.p7 | 2:224579937 | GTGGGCAAAACCCCA[C/G]ACAGTAAAAATGGTA | 8452 |