SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs122571 | snp | A/G | 0.466515 | 0.124985 | upstream-variant-2KB | CUL1 | GRCh38.p7 | 7:148697503 | CCACATTTCAATAGA[A/G]GGATCACACAGACCA | 8454 |
rs243477 | snp | A/G | 0.417845 | 0.185278 | intron-variant | CUL1 | GRCh38.p7 | 7:148759062 | CTTTAACTGTTGTTG[A/G]AAACAGTATAGGAAA | 8454 |
rs243478 | snp | A/G | 0.493107 | 0.0583 | intron-variant | CUL1 | GRCh38.p7 | 7:148757676 | cagcagtatgaaaac[A/G]gactaatacaggacc | 8454 |
rs243479 | snp | C/T | 0.337841 | 0.23406 | intron-variant | CUL1 | GRCh38.p7 | 7:148756520 | GTGAAACCCTGTCTC[C/T]ACTAAAAATACAAAA | 8454 |
rs243480 | snp | G/T | 0.358515 | 0.225221 | intron-variant | CUL1 | GRCh38.p7 | 7:148755813 | GCCATGTAAAAACCG[G/T]ATCATCTCTTGAGAC | 8454 |
rs243481 | snp | G/T | 0.493477 | 0.0567349 | intron-variant | CUL1 | GRCh38.p7 | 7:148755330 | GCAAATTTCCCTGGG[G/T]TCACAGTATAGACGT | 8454 |
rs243482 | snp | G/T | 0.493568 | 0.0563433 | intron-variant | CUL1 | GRCh38.p7 | 7:148753429 | CACACTCCTGAGAAA[G/T]AGAGAGATGTATAAA | 8454 |
rs243483 | snp | C/T | 0.362732 | 0.22314 | intron-variant | CUL1 | GRCh38.p7 | 7:148752071 | CAGACTGGAGTGCAA[C/T]GGCGTGATCTCAGCT | 8454 |
rs243484 | snp | A/C | 0.369346 | 0.219673 | intron-variant | CUL1 | GRCh38.p7 | 7:148751563 | TAAGTGACAAAGTGA[A/C]AAGAGAGGTTTTTTT | 8454 |
rs243485 | snp | G/T | 0.5 | 0 | intron-variant | CUL1 | GRCh38.p7 | 7:148751551 | TGACAAGAGAGGTTT[G/T]TTTTTTTTTTTTTTT | 8454 |
rs243486 | snp | G/T | 0.35894 | 0.225016 | intron-variant | CUL1 | GRCh38.p7 | 7:148751129 | GAGTTGCCAACTTAG[G/T]GCTACAAAGCGGCTA | 8454 |
rs243487 | snp | C/T | 0.362523 | 0.223246 | intron-variant | CUL1 | GRCh38.p7 | 7:148751119 | CTTAGTGCTACAAAG[C/T]GGCTATCCAGCACCC | 8454 |
rs243488 | snp | C/T | 0.364193 | 0.222396 | intron-variant | CUL1 | GRCh38.p7 | 7:148749557 | gggtgcagtgtgtgg[C/T]gcctcaaagccattC | 8454 |
rs243489 | snp | A/G | 0.364401 | 0.222289 | intron-variant | CUL1 | GRCh38.p7 | 7:148749372 | ctggagagctgtggc[A/G]caatcttggctcact | 8454 |
rs243490 | snp | G/T | 0.354881 | 0.226936 | intron-variant | CUL1 | GRCh38.p7 | 7:148749262 | gcccagctaattttc[G/T]tatttttagtagaga | 8454 |
rs243491 | snp | C/T | 0.47666 | 0.105476 | intron-variant | CUL1 | GRCh38.p7 | 7:148749081 | TTGTTTTGGTTAACT[C/T]TGTAATTTCCTTTTT | 8454 |
rs243492 | snp | A/G | 0.476401 | 0.106032 | intron-variant | CUL1 | GRCh38.p7 | 7:148748716 | CAGAACGGGGGGGCC[A/G]TTATTTCACATGTGC | 8454 |
rs243493 | snp | C/G | 0.497091 | 0.0380279 | intron-variant | CUL1 | GRCh38.p7 | 7:148747786 | GTTGTGTCAAATTTA[C/G]TGTTTAATTTTAATG | 8454 |
rs243494 | snp | G/T | 0.430136 | 0.173352 | intron-variant | CUL1 | GRCh38.p7 | 7:148746369 | AGAACAAGGCTGCAC[G/T]CAAGTGTGCACTGAT | 8454 |
rs243495 | snp | A/C | 0.496937 | 0.0390173 | intron-variant | CUL1 | GRCh38.p7 | 7:148744308 | gcaagaacaaagaaa[A/C]tttttaaggggagaa | 8454 |
rs243496 | snp | A/G | 0.426966 | 0.176587 | intron-variant | CUL1 | GRCh38.p7 | 7:148743723 | ccaggctggtcttga[A/G]ctcctggcatcaggc | 8454 |
rs243497 | snp | A/G | 0.468249 | 0.121932 | intron-variant | CUL1 | GRCh38.p7 | 7:148743650 | tcccaatgtgctggg[A/G]ttacagatgtgagcc | 8454 |
rs243498 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CUL1 | GRCh38.p7 | 7:148742775 | gtctctactaaaaat[A/T]caaaaattagctggg | 8454 |
rs243499 | snp | A/C | 0.427423 | 0.176128 | intron-variant | CUL1 | GRCh38.p7 | 7:148742659 | agccaagaacatgca[A/C]tgcactccagcctgg | 8454 |
rs243500 | snp | C/G | 0.478603 | 0.101197 | intron-variant | CUL1 | GRCh38.p7 | 7:148742273 | cagccacgtggaact[C/G]tgagtccgttaaacc | 8454 |
rs243501 | snp | C/G | 0.463774 | 0.129618 | intron-variant | CUL1 | GRCh38.p7 | 7:148741053 | acatggatgaagtta[C/G]aaaacattatactaa | 8454 |
rs243502 | snp | A/G | 0.434831 | 0.168337 | intron-variant | CUL1 | GRCh38.p7 | 7:148740113 | gtaagccaaggttgc[A/G]ccattgcactccggc | 8454 |
rs243503 | snp | C/G | 0.434831 | 0.168337 | intron-variant | CUL1 | GRCh38.p7 | 7:148739014 | AGGACAGGGCCGGAG[C/G]CTCCCCGCTGCTCTC | 8454 |
rs243504 | snp | C/T | 0.497722 | 0.0336691 | intron-variant | CUL1 | GRCh38.p7 | 7:148738301 | CCTTCTGGGCACCTG[C/T]CCAGTGCCAGGTACC | 8454 |
rs243505 | snp | C/T | 0.497641 | 0.0342639 | intron-variant | CUL1 | GRCh38.p7 | 7:148738247 | AACAGACTGCCTTCC[C/T]GGAGTTCAGCATCTA | 8454 |
rs243506 | snp | A/T | 0.493013 | 0.058691 | intron-variant | CUL1 | GRCh38.p7 | 7:148737572 | ATAAATAAATATAAA[A/T]ATATATATATATACA | 8454 |
rs243507 | snp | C/T | 0.436692 | 0.166271 | intron-variant | CUL1 | GRCh38.p7 | 7:148737508 | ACATTAACAAGTTAA[C/T]CTGTACCAAATGGCA | 8454 |
rs243508 | snp | A/T | 0.436408 | 0.16659 | intron-variant | CUL1 | GRCh38.p7 | 7:148737402 | GTACGTGCATTTCTG[A/T]AAAGAAATATCCCAT | 8454 |
rs243509 | snp | C/T | 0.497387 | 0.0360476 | intron-variant | CUL1 | GRCh38.p7 | 7:148736542 | GCCAAGGTGGGAGGA[C/T]TGCTTGAAGCCAGGA | 8454 |
rs243510 | snp | C/T | 0.433527 | 0.169758 | intron-variant | CUL1 | GRCh38.p7 | 7:148735442 | CTGCCACCTGAGCAC[C/T]CCCCTGCAGTGCAGC | 8454 |
rs243511 | snp | G/T | 0.433236 | 0.170072 | intron-variant | CUL1 | GRCh38.p7 | 7:148733056 | CAGGTTCCTGGAGCT[G/T]ATCCACAGAGAAAGG | 8454 |
rs243512 | snp | A/G | 0.496905 | 0.0392151 | intron-variant | CUL1 | GRCh38.p7 | 7:148732970 | GCACAAAGCCTGACA[A/G]CTGTAGCCATTATTT | 8454 |
rs243513 | snp | C/T | 0.371582 | 0.218444 | intron-variant | CUL1 | GRCh38.p7 | 7:148732714 | CATACAAAGTCTCAC[C/T]GCCTTATGAGCAAAA | 8454 |
rs243514 | snp | C/T | 0.497151 | 0.037632 | intron-variant | CUL1 | GRCh38.p7 | 7:148730781 | ACTTTTGCTCGATGT[C/T]CTATCCCTTTTGATC | 8454 |
rs243515 | snp | G/T | 0.472616 | 0.113763 | intron-variant | CUL1 | GRCh38.p7 | 7:148729580 | CAAACAGCTAATAAA[G/T]AGGAAAAATCATACA | 8454 |
rs243516 | snp | A/C | 0.497329 | 0.0364438 | intron-variant | CUL1 | GRCh38.p7 | 7:148729179 | TCCAAGTATATGAAG[A/C]TAATGACAAATACAA | 8454 |
rs243517 | snp | A/T | 0.497329 | 0.0364438 | intron-variant | CUL1 | GRCh38.p7 | 7:148728823 | CAGAGCTCTGTGTAA[A/T]CTAAGGCACATTTAG | 8454 |
rs243518 | snp | A/G | 0.398354 | 0.201224 | intron-variant | CUL1 | GRCh38.p7 | 7:148727936 | TGACAGCCTATTCAG[A/G]ATTAGGATGACACCG | 8454 |
rs243519 | snp | C/T | 0.49607 | 0.0441545 | intron-variant | CUL1 | GRCh38.p7 | 7:148726532 | AAAAACCACCAACAA[C/T]TGCCTATTTGTTAAA | 8454 |
rs243520 | snp | A/G | 0.434109 | 0.169127 | intron-variant | CUL1 | GRCh38.p7 | 7:148726468 | CGATAGCTTTAAAGA[A/G]TTAATAAGTCAGTCC | 8454 |
rs243521 | snp | A/G | 0.434398 | 0.168811 | intron-variant | CUL1 | GRCh38.p7 | 7:148724479 | GCTCCCGGAGCCCGC[A/G]TGAGTTTTTACCACA | 8454 |
rs243522 | snp | C/T | 0.497271 | 0.0368399 | intron-variant | CUL1 | GRCh38.p7 | 7:148723417 | GCAGTTGTCCTTGGA[C/T]GTGTGAACCTGAGGT | 8454 |
rs243523 | snp | G/T | 0.336017 | 0.234736 | intron-variant | CUL1 | GRCh38.p7 | 7:148722392 | GGAGGAGTTTCGCAT[G/T]CATGGATGAGGACTC | 8454 |
rs243524 | snp | A/C | 0.468349 | 0.121752 | intron-variant | CUL1 | GRCh38.p7 | 7:148721089 | AGACTGGAAAGTTCA[A/C]GCTCAGAAATTCTTG | 8454 |
rs243525 | snp | C/T | 0.497803 | 0.033074 | intron-variant | CUL1 | GRCh38.p7 | 7:148721048 | GAAATTATTAAATTC[C/T]CTTTAAGTTTTAAAT | 8454 |
rs243526 | snp | A/G | 0.497695 | 0.0338674 | intron-variant | CUL1 | GRCh38.p7 | 7:148719981 | GCATGTACAAGCTAC[A/G]TTTCACAAATGAGGA | 8454 |
rs243527 | snp | A/C | 0.497749 | 0.0334707 | intron-variant | CUL1 | GRCh38.p7 | 7:148719012 | CAGTAGCTAAGTTTT[A/C]TCTCTACTTACTTAA | 8454 |
rs243528 | snp | A/G | 0.474272 | 0.110462 | intron-variant | CUL1 | GRCh38.p7 | 7:148718648 | CCAAAGTGGAATAAC[A/G]CAAATGTCCACCAAC | 8454 |
rs243529 | snp | C/T | 0.497329 | 0.0364438 | intron-variant | CUL1 | GRCh38.p7 | 7:148716709 | TAAATTCTTAGCAGA[C/T]ACTTAACTGAAAACA | 8454 |
rs243530 | snp | A/G | 0.396182 | 0.202807 | intron-variant | CUL1 | GRCh38.p7 | 7:148715526 | CAAGAGACAGAATAT[A/G]TAAGAGAACCAGGAG | 8454 |
rs243531 | snp | C/T | 0.497329 | 0.0364438 | intron-variant | CUL1 | GRCh38.p7 | 7:148715421 | GGAAAAGGTCTATTA[C/T]GAAAAGTCACTGACT | 8454 |
rs243532 | snp | C/T | 0.434831 | 0.168337 | intron-variant | CUL1 | GRCh38.p7 | 7:148715279 | GTGAGAAGACAATGG[C/T]GGACTCTGTTGCTAG | 8454 |
rs243533 | snp | C/T | 0.396546 | 0.202545 | intron-variant | CUL1 | GRCh38.p7 | 7:148714730 | TGTTCATGCTTTCCA[C/T]TGCCCTCTAAAATGA | 8454 |
rs243534 | snp | A/G | 0.497502 | 0.035255 | intron-variant | CUL1 | GRCh38.p7 | 7:148713966 | ttgggaggccgaggc[A/G]ggtggatcacctgag | 8454 |
rs243535 | snp | G/T | 0.436123 | 0.166908 | intron-variant | CUL1 | GRCh38.p7 | 7:148713031 | AGGGAACTGGAACTT[G/T]TTAAAAAATCAAATA | 8454 |
rs243536 | snp | C/T | 0.473818 | 0.111381 | intron-variant | CUL1 | GRCh38.p7 | 7:148712849 | CAAATTGCAAACAGC[C/T]AATATGGAAATGCGT | 8454 |
rs243537 | snp | C/T | 0.435694 | 0.167385 | intron-variant | CUL1 | GRCh38.p7 | 7:148711186 | ATGAGGAGAAACATA[C/T]ATGCACAGAAGTGTA | 8454 |
rs243538 | snp | C/T | 0.390277 | 0.206936 | intron-variant | CUL1 | GRCh38.p7 | 7:148707287 | TCCTGGCCTCTATGG[C/T]ACTTCCCACACTGTG | 8454 |
rs243539 | snp | A/G | 0.492582 | 0.0604491 | intron-variant | CUL1 | GRCh38.p7 | 7:148706825 | TAAAACAAGTAGAGT[A/G]GTAAGGCAGAGCTCC | 8454 |
rs243540 | snp | C/T | 0.432797 | 0.170544 | intron-variant | CUL1 | GRCh38.p7 | 7:148706220 | CAGAAGTCTTTTGAA[C/T]TTCAGACTGTTTCAT | 8454 |
rs243541 | snp | A/T | 0.431177 | 0.172264 | intron-variant | CUL1 | GRCh38.p7 | 7:148706151 | AATCTAAACGGGGAA[A/T]TCACATGTTTCATAT | 8454 |
rs243542 | snp | C/T | 0.496968 | 0.0388195 | intron-variant | CUL1 | GRCh38.p7 | 7:148706102 | CTGAAGGTAATTTTA[C/T]TTTCCCCTTGGGGAC | 8454 |
rs243543 | snp | C/G | 0.496999 | 0.0386216 | intron-variant | CUL1 | GRCh38.p7 | 7:148705892 | AAATGGCAAGCAAAC[C/G]TTTTAAAGATTTTAC | 8454 |
rs243544 | snp | A/T | 0.439224 | 0.163383 | intron-variant | CUL1 | GRCh38.p7 | 7:148705618 | GAGGTCTGAGCTGTC[A/T]GCCTTTTTCCCCCGT | 8454 |
rs243545 | snp | C/T | 0.497151 | 0.037632 | intron-variant | CUL1 | GRCh38.p7 | 7:148704316 | TCACCATAAGTAGTT[C/T]ATTTTTTAATCTACG | 8454 |
rs243546 | snp | A/G | 0.427423 | 0.176128 | intron-variant | CUL1 | GRCh38.p7 | 7:148701542 | AACCTGGGGGGAAAA[A/G]CCTGATCGTGTTTCC | 8454 |
rs243547 | snp | C/G | 0.437118 | 0.165792 | intron-variant | CUL1 | GRCh38.p7 | 7:148701208 | GTAGCCAAAAATCAG[C/G]GCATGTTTTCAAACG | 8454 |
rs243548 | snp | C/T | 0.384401 | 0.210799 | intron-variant, upstream-variant-2KB | CUL1 | GRCh38.p7 | 7:148699457 | CGGGTCCCGGCGTCC[C/T]GCGGAGGTCGCCTCA | 8454 |
rs243549 | snp | G/T | 0.493386 | 0.0571263 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL1 | GRCh38.p7 | 7:148698580 | cccgggggcgcccct[G/T]ccgcggccgaggccc | 8454 |
rs243550 | snp | C/G | 0.369754 | 0.219451 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | CUL1 | GRCh38.p7 | 7:148698392 | GCGAGCGGGGCTGAG[C/G]TGCTTGGGTCGGGGA | 8454 |
rs243551 | snp | C/G | 0.46845 | 0.121572 | upstream-variant-2KB | CUL1 | GRCh38.p7 | 7:148698032 | CCCTTCAGACTTTCA[C/G]TAACTCCTGTTTGGC | 8454 |
rs726078 | snp | C/G/T | 0.00847442 | 0.0645399 | intron-variant | CUL1 | GRCh38.p7 | 7:148778797 | TTGCCTACACTACCT[C/G/T]TGAGGGTACACTCAG | 8454 |
rs740951 | snp | A/C | 0.446249 | 0.154875 | intron-variant | CUL1 | GRCh38.p7 | 7:148773068 | TCTCCCATTCCCATT[A/C]ATCCCTCATGATAAT | 8454 |
rs758880 | snp | C/T | 0.490836 | 0.0670685 | intron-variant | CUL1 | GRCh38.p7 | 7:148780497 | ACTCACCCAGCGGCT[C/T]GAGCCAGGCACCCAG | 8454 |
rs933436 | snp | A/C | 0.41275 | 0.189769 | intron-variant | CUL1 | GRCh38.p7 | 7:148790237 | GTTTCTAAGTAAAGC[A/C]CACTGTTCCAAGCTT | 8454 |
rs1008347 | snp | C/G | 0.0901694 | 0.192235 | intron-variant | CUL1 | GRCh38.p7 | 7:148714887 | Ctttgttttttgttt[C/G]tttgtttgtttTGTG | 8454 |
rs1014095 | snp | A/G | 0.385444 | 0.210131 | intron-variant | CUL1 | GRCh38.p7 | 7:148766768 | AGCAATATCAAAACT[A/G]CAGATAATTATAAAT | 8454 |
rs1014096 | snp | A/G | 0.395453 | 0.203331 | intron-variant | CUL1 | GRCh38.p7 | 7:148766375 | actttgggtggctga[A/G]gcaggaggattgctc | 8454 |
rs1019057 | snp | A/T | 0.375 | 0.216506 | intron-variant | CUL1 | GRCh38.p7 | 7:148726851 | aaaaaaaaaaaaaaa[A/T]ttttttttaaattag | 8454 |
rs1019058 | snp | A/G | 0.434831 | 0.168337 | intron-variant | CUL1 | GRCh38.p7 | 7:148727151 | ctaaatattcgttaa[A/G]ACTAAGTAGTCACTA | 8454 |
rs1019059 | snp | A/G | 0.434687 | 0.168495 | intron-variant | CUL1 | GRCh38.p7 | 7:148727155 | atattcgttaaaACT[A/G]AGTAGTCACTAAAAT | 8454 |
rs1019218 | snp | A/G | 0.415399 | 0.187465 | intron-variant | CUL1 | GRCh38.p7 | 7:148791872 | CAGGTAGCACGTGTT[A/G]GTTCCTGATTGCTGA | 8454 |
rs1029888 | snp | A/G | 0.336474 | 0.234568 | intron-variant | CUL1 | GRCh38.p7 | 7:148772624 | GCATTCTAATTCAGA[A/G]TTCTTGACATCACGT | 8454 |
rs1029889 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | CUL1 | GRCh38.p7 | 7:148772093 | TGTACGATGAGTTTA[C/T]TGAAAGTATCATAAA | 8454 |
rs1062892 | snp | A/C | | | utr-variant-3-prime | CUL1 | GRCh38.p7 | 7:148801034 | TAAAGGATTTCTGTA[A/C]AAGTCGCATTGGGTT | 8454 |
rs1558419 | snp | A/G | 0.404907 | 0.196224 | intron-variant | CUL1 | GRCh38.p7 | 7:148783141 | TGGCCAAAGGAAGGC[A/G]GCGACAATGGAAGGC | 8454 |
rs1558420 | snp | A/C | 0.398714 | 0.200958 | intron-variant | CUL1 | GRCh38.p7 | 7:148783022 | AAAGCCCACACTGGG[A/C]AGCAGGTGCTGTTTT | 8454 |
rs1802351 | snp | C/T | | | utr-variant-3-prime | CUL1 | GRCh38.p7 | 7:148800586 | TACTTGGCTTAACCC[C/T]TCTGGAAGGGTCTGA | 8454 |
rs1962809 | snp | A/G | 0.300421 | 0.244863 | intron-variant | CUL1 | GRCh38.p7 | 7:148791911 | tgagccactgcaccc[A/G]gccCTAAAGTATCTT | 8454 |
rs1963814 | snp | A/G | 0.067446 | 0.170804 | intron-variant | CUL1 | GRCh38.p7 | 7:148772289 | tagctgggattacag[A/G]tgcctgctaacacgc | 8454 |
rs2005853 | snp | C/T | 0.399073 | 0.200692 | intron-variant | CUL1 | GRCh38.p7 | 7:148779996 | GAACCTGGAGTCTGA[C/T]GTTCGAGGGCAGGAA | 8454 |
rs2007404 | snp | A/G | 0.465521 | 0.126691 | intron-variant | CUL1 | GRCh38.p7 | 7:148790303 | ACGTTCCAACTAGAT[A/G]AAAGGACAGCATTAT | 8454 |
rs2058388 | snp | C/G | 0.236434 | 0.249632 | intron-variant | CUL1 | GRCh38.p7 | 7:148789330 | ATAGTGTATGTTTCA[C/G]TTATTACTGGGAAAC | 8454 |
rs2072406 | snp | C/T | 0.416218 | 0.186739 | intron-variant | CUL1 | GRCh38.p7 | 7:148786668 | TTCAGAGGCCATCTA[C/T]AAATAACATTACAAA | 8454 |
rs2109709 | snp | A/C | 0 | 0 | intron-variant | CUL1 | GRCh38.p7 | 7:148778874 | CCTTCACCATTTCAT[A/C]TACATAAACTGGTGC | 8454 |