SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs148393553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108057375 | ATTTGCATAGTTTCA[A/G]AGTATCGTCCCCAAG | 8065 |
rs148482180 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CUL5 | GRCh38.p7 | 11:108011946 | TCTTTTTTAATATTG[A/G]AATTTGACTCTAATA | 8065 |
rs148494988 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108043345 | TCCAAGAGTGCTAGG[A/T]TTACAGACATGAGCC | 8065 |
rs148528006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033702 | CTGGTTCATTTAAAT[G/T]TGAGCCCTTCATTTC | 8065 |
rs148547589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108091965 | AAAATAACAATACTC[C/T]ATGTCTACAAAAAAT | 8065 |
rs148551653 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108061816 | TTGAACCAGTTCCAC[A/G]TGGCCTGGGAGTCCT | 8065 |
rs148600686 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108097170 | CTACAGGTGCATGCC[C/G]CACGCTGGCTAATTT | 8065 |
rs148604499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108017551 | GGTAGCGAAAACAAC[A/G]TGATAAGAATGTTCA | 8065 |
rs148684516 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108038822 | CATGTTAATCGTTAA[C/T]ATTTAGGTTGCTTAT | 8065 |
rs148701250 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | CUL5 | GRCh38.p7 | 11:108081243 | CAGTGAGCCGAGATC[A/G]TGCCATTACACTCCA | 8065 |
rs148738149 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CUL5 | GRCh38.p7 | 11:108071178 | CCTTTTGATGATATG[A/G]CTGTATATGTAGTAT | 8065 |
rs148761181 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108023458 | TTAGATTTTTAAAAA[C/T]GAAAACAAAATTTTA | 8065 |
rs148790756 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108065586 | TGAAAGGGTGGTGGT[A/G]AGTTCAATGCAGTAT | 8065 |
rs148830013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108035985 | GCCATATTTCAAGTC[C/T]GAGTGATCAGCGAGA | 8065 |
rs148864451 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108063861 | CCACCATCATTATAC[A/G]AGGGTTCCTTTTTCT | 8065 |
rs148917798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108019411 | AATTATCTAAAATAC[A/G]ACAACTGAGTTCCTT | 8065 |
rs148961193 | in-del | -/CTTT | 0.00517822 | 0.0506191 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107232 | AAAATGAAATGTTAG[-/CTTT]CTTTCTTTTACTTTT | 8065 |
rs148992074 | snp | C/G | 0.000153988 | 0.00877328 | missense | CUL5 | GRCh38.p7 | 11:108095630 | CCAGAGAGAAAATCA[C/G]CTTTGAAAATCTTAA | 8065 |
rs149013701 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CUL5 | GRCh38.p7 | 11:108083123 | TGCTCTGACCGGAAC[A/G]TCTACTACAGTAACA | 8065 |
rs149037069 | snp | C/T | 0.000275862 | 0.0117412 | intron-variant | CUL5 | GRCh38.p7 | 11:108073513 | GTATATATTCCTATA[C/T]ATATAAAAAACACTT | 8065 |
rs149070760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087615 | AAAAATTTTTTAATT[C/T]GTGTATGTTTGTGTC | 8065 |
rs149072190 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108009848 | AATTCCGAGTCAGAC[C/G]AGCAGTGCCTCCCAC | 8065 |
rs149084814 | in-del | -/TTCTC | 0.147929 | 0.228214 | intron-variant | CUL5 | GRCh38.p7 | 11:108016233 | AGAGAGGTTTTTCTT[-/TTCTC]TTCTCTTCTCTTCTC | 8065 |
rs149092145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108067756 | TTAGTTATATATTGT[C/T]AGATTTACCTATGCT | 8065 |
rs149153584 | in-del | -/TCTT | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108082275 | CCCTTCCTTCTTCTC[-/TCTT]TCTTTCTGTTTTTTT | 8065 |
rs149242351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108101433 | GTTCATTCTTTTTCT[A/G]GTTGCTAAGGGCCCC | 8065 |
rs149307104 | in-del | -/TTATTTAT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080954 | CATGAAGATTTATCA[-/TTATTTAT]TTATTTATTTATTTA | 8065 |
rs149331459 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CUL5 | GRCh38.p7 | 11:108056785 | CAAGTAGAGTTACAG[A/G]AGTGGGAATGGAAAA | 8065 |
rs149353467 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CUL5 | GRCh38.p7 | 11:108075546 | ACAGCAGGCTCTAGA[A/G]GTGACTTGTCAGGGA | 8065 |
rs149384884 | snp | C/T | 1.67826e-05 | 0.00289673 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108089584 | ATTAGACATCTCTGC[C/T]GATAGTGAAATTGAA | 8065 |
rs149386172 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108011210 | GAGTAAGTCACTGTT[C/G]TACTTACAAAACCTC | 8065 |
rs149407606 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108041304 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCTGTTGCC | 8065 |
rs149508940 | snp | A/C | 0.0275645 | 0.114116 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106422 | AATGCAAAAGTGGGT[A/C]ACACTACATTCATAG | 8065 |
rs149546214 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108017131 | CAGTGGCTCACACCT[C/G]TAATCCAAGCACTTT | 8065 |
rs149564386 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108037653 | AATATTGTCTACCAG[C/G]GAAGCTAATTAGGGG | 8065 |
rs149570063 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080962 | TTTATCATTATTTAT[A/T]TATTTATTTATTTAT | 8065 |
rs149575444 | snp | A/C/G | 0.000350858 | 0.0132407 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108052776 | TTTTGATTCTCAGCT[A/C/G]GTTATTGGAGTAAGA | 8065 |
rs149598279 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108051829 | GAGAATAAACATTTT[A/C]CATGTATTATCATAG | 8065 |
rs149611823 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108065292 | CCTGGCAAAGTGCTG[A/G]GATTACAGGCATGAG | 8065 |
rs149666803 | snp | A/G | 0.000531491 | 0.016293 | missense | CUL5 | GRCh38.p7 | 11:108078206 | GTTAATGATGCTACC[A/G]TATTTAAACTTGAAT | 8065 |
rs149682880 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108091685 | CAGAGTCAGATCCTG[A/T]CTCTCTCACTCACAC | 8065 |
rs149700981 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CUL5 | GRCh38.p7 | 11:108012751 | ACAGGCACACGCCAC[C/T]ACACCCAGCTTATTT | 8065 |
rs149717141 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108029626 | GATATGCTCTTCAGT[C/T]TAATAGAGAATAGGT | 8065 |
rs149738341 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108085481 | CTGTTTGGGATAATG[A/C]AGAAGTTCTAGAAAT | 8065 |
rs149767115 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | CUL5 | GRCh38.p7 | 11:108062276 | CTTGGCTTCCTCTTG[G/T]AATAGAATCTCCTGG | 8065 |
rs149771708 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032503 | ACAGAGCAAGACCCT[A/G]TCTTAAAAACAAACA | 8065 |
rs149844194 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108019126 | GGGAGGATGTGCATG[A/G]GTAATAAGCAAATGC | 8065 |
rs149880400 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008275 | ACTTGATTGGATTCT[C/T]TAAGTAGGCCCATCC | 8065 |
rs149897242 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108054167 | TTTCTGTAGACACAT[A/G/T]ATTTTACTATGTTGC | 8065 |
rs149927000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108067261 | CCTGTTATAATAATT[G/T]GTTTAACCTCTCAAG | 8065 |
rs149931439 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108080545 | GGACTACAGGTGTGT[A/G]CCACCACGCCCAGCT | 8065 |
rs149980090 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105328 | TCTCCTGCTCTGATA[C/T]AGTTATGTAACTGAT | 8065 |
rs150054840 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108058949 | GAACAGGCATGTTGA[A/C/G]AGCAAAAAGTAACAC | 8065 |
rs150083400 | snp | C/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108035414 | TTCATAGTTTCTGGC[C/T]CCACAGGAGGATATC | 8065 |
rs150100218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108076624 | TTATCCATTGATGGA[C/T]GCTGAGGTTGTGTCC | 8065 |
rs150158001 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CUL5 | GRCh38.p7 | 11:108020584 | ACAGGGTCTCACCAC[A/G]TTGCCCAGGCTGGTC | 8065 |
rs150204995 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108010275 | CAGTCACTTTTGCAC[C/T]AGCCTAATACAAAGG | 8065 |
rs150208090 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CUL5 | GRCh38.p7 | 11:108055926 | GTGAGCCACTGCACC[C/T]GGCCACCTGGCTAAT | 8065 |
rs150233382 | in-del | -/T | 0.0154538 | 0.0865337 | intron-variant | CUL5 | GRCh38.p7 | 11:108043384 | TGGCCCAGTCTCTTC[-/T]TTTAGACTCTAGATT | 8065 |
rs150319464 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025859 | AAACCCCTAGCGGCT[-/G]GTTTGGGTTTCCCCT | 8065 |
rs150365344 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108060392 | GTGGGGGAACTTAAG[A/G]TAATTTTTAGTTCAA | 8065 |
rs150382024 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107163 | CCTGAGTTCTGTCAA[C/T]TTTTTTATTTAAGTC | 8065 |
rs150415122 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108050704 | ATTACTTTTCTCCCT[G/T]TCTCAAAAATCCCCT | 8065 |
rs150418639 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108094222 | CCTTGTAATACCGTA[C/T]TTTGTTTCTAAGTAG | 8065 |
rs150467939 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108045294 | GCTTTATTGTGATTT[A/C]AGTGACTAATTTTTT | 8065 |
rs150521053 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108012299 | CCACCCCAAACAGCA[A/G]TTGTTTAAACCTTTT | 8065 |
rs150524645 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108027965 | TCTTTGTCTCCTTTG[C/T]TAGTTCTTACTCCTC | 8065 |
rs150541654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068986 | CTTGGGGCCAGGCCT[A/G]ATGGTTCACACCTGT | 8065 |
rs150546641 | snp | A/C | 3.36666e-05 | 0.0041027 | missense | CUL5 | GRCh38.p7 | 11:108073421 | TTGAGCAGTTACTTA[A/C]ACTATTTAATAGATT | 8065 |
rs150571763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108084633 | GTACAACATTACTAG[C/T]CCTATGAAGACAGAT | 8065 |
rs150572929 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007554 | AGTCAGAGTTGTAGC[A/G]GTGGTGTTTCCAGAA | 8065 |
rs150698766 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108074884 | TATAGACATGGTGGG[C/T]GTGGTGTGAAGTCTT | 8065 |
rs150744033 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108097342 | AATTAATTATTACCT[A/G]TGGAGGAAATAGCTG | 8065 |
rs150760318 | in-del | -/AT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108055615 | CTGCCTGACTAATAA[-/AT]ATATATATATATATA | 8065 |
rs150782988 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108047764 | ACTAATTTAGAGATA[C/T]AGTTTCTACTTGCAT | 8065 |
rs150788059 | in-del | -/AAAT/AAT/TAAAT | 0.246769 | 0.249979 | intron-variant | CUL5 | GRCh38.p7 | 11:108063661 | AATAAAATTTAAAAA[-/AAAT/AAT/TAAAT]AAATAAATAAATAGT | 8065 |
rs150833134 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | CUL5 | GRCh38.p7 | 11:108079589 | GTCATTTATTGAATT[G/T]AATGTTTATGTTTTT | 8065 |
rs150904395 | snp | A/G | 0.0138799 | 0.0821421 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104880 | GAGCTGGTCAATGCA[A/G]CATTGGGAAACGGCA | 8065 |
rs150910216 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | CUL5 | GRCh38.p7 | 11:108036949 | TGGTTCACTCTCCCC[A/T]CTCCTGTTTCTCCCC | 8065 |
rs151012227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108076179 | CTGGGACTACAGGCA[C/T]GCACCACTATGTTTG | 8065 |
rs151062637 | snp | C/G | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108066663 | TAACTATTGTTTCTA[C/G]CACTAGGTTTAGGAG | 8065 |
rs151064693 | snp | A/C | 3.29625e-05 | 0.00405958 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108095652 | AAATCTTAAGCTTGC[A/C]ACTGAACTCCCTGAT | 8065 |
rs151097110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108049406 | GAGTGCAGTGGTGCA[A/G]TCATGGCTCACTGTA | 8065 |
rs151115184 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108062052 | GTGGGAATTACAATT[C/T]GAGATGAAATTTGGC | 8065 |
rs151171303 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CUL5 | GRCh38.p7 | 11:108044916 | ACAGGTGCACACCAC[C/T]ACGCCTGGCTAATTT | 8065 |
rs151240707 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108093822 | CCACCTCAGCCTTCC[A/G/T]AGTAGCTGGGACTAT | 8065 |
rs151262207 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108029269 | CCACGGCCCATTTGT[C/G]TGAGAAGAAGAGTGC | 8065 |
rs151279207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071582 | TGAGACCGTCTTGCC[C/T]TGTCACCCAGGCTGA | 8065 |
rs151313368 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | CUL5 | GRCh38.p7 | 11:108024429 | TCTTGTCTCAAAAAA[A/T]AATAATAATAATAAT | 8065 |
rs180671373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031286 | ATGAAAATCACCTGA[C/T]CCTGGGAGGTAGAGG | 8065 |
rs180680794 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108010664 | ACAGTGCCTGGCACT[C/T]AATTAGTATAATACA | 8065 |
rs180687923 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108023099 | ACTAAAAAAAATAGC[C/T]GGGCATGGTGGCACA | 8065 |
rs180701212 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108048108 | AAAAAGATTTTTAAA[C/T]GCTTAAGAAATTTTT | 8065 |
rs180803006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108072858 | AAACATTAAATTTTT[A/T]AAAATACAGAATTGA | 8065 |
rs180803251 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108091128 | GCAATCTTGACTCAC[C/T]GAAACCTCTGTCTCC | 8065 |
rs180828125 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057035 | ACCTGGATGGGAATG[A/T]TACAGTTTTATAAGG | 8065 |
rs180836541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108040399 | GGTGGATCACCTGAG[G/T]TCAGGAGTTCGATAC | 8065 |
rs180837974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108061920 | GAGAGAGAGAGAATG[C/T]GCAGGAGAAACTGCC | 8065 |
rs180854650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100791 | ATCCCAACACTTTGG[G/T]AGGCCGAGGCGGGTG | 8065 |
rs180875801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108082198 | TTGTAAATTGAATTG[C/T]TCTTCCTTCCTCCCT | 8065 |
rs180894819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108077939 | GGTCGACAGAGTGAG[A/T]CTTCATCTCAAAAAA | 8065 |
rs180903999 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104663 | GTGAATTTGATTTGT[A/T]CCCACCAGGAGAAAT | 8065 |
rs180924879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108051789 | AACACACCAATATAT[C/T]TGAAATTCAACCATG | 8065 |
rs180928039 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108066461 | TCACTCTACTCCAAT[A/G]AGAAATATTTTTTTA | 8065 |
rs180930953 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108086087 | ATATAATTGGAGTCA[C/T]AGAGCATAGAAAAGA | 8065 |
rs180933712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108044729 | TGATTTACAACTTGG[C/T]AATTTTTTTACTTTT | 8065 |
rs180942879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016656 | AGGAAATAGATGCCT[C/T]ATATGCTCTGTAAGG | 8065 |
rs180943944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096886 | ACTTAATTTTTATAC[C/T]GAGAATGTGTTCAAA | 8065 |
rs180958846 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | CUL5 | GRCh38.p7 | 11:108027365 | CAAACTCCGCCTCCC[A/T]GGTTCAAGCAATTCT | 8065 |
rs180959458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108036687 | TTCACCATGTTGGCC[A/G]GGATGGTCTCGAACT | 8065 |
rs180975014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108059318 | ATGCTAGTTGGGGAT[A/G]ATAAGATAGACCTAG | 8065 |
rs181365997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108063009 | CACCACCACGCCCGG[C/G]TAATTTTGTATTTTT | 8065 |
rs181371136 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108082536 | CCCACCTTAGCCCCT[C/T]AAAGTGCTAGGATTA | 8065 |
rs181375520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108101349 | GCAGCTATGAAGTAG[C/T]TGATTATCTTTGGGA | 8065 |
rs181382635 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108010971 | AGTTAACTATGATCA[C/T]GCCACTGCTCTGTGA | 8065 |
rs181386861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048321 | ATTAACACAACTGTT[C/T]TATTTGTTCACAATT | 8065 |
rs181388397 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CUL5 | GRCh38.p7 | 11:108031334 | TATGCCACTGCACTC[C/T]AGCCTGGGCAACAGA | 8065 |
rs181401048 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108026536 | GCCTTCTCCTCTTAG[C/G]CTGTAGTCACTTCCT | 8065 |
rs181414469 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108055559 | AAGGGCCCCTCCTGC[C/T]TCAGCCTCCTAAGTA | 8065 |
rs181438425 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108020960 | ATTTAGGTCTACCAT[G/T]TTTTATCTTTCATAC | 8065 |
rs181480958 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037107 | GGGCCTCTTCCCACC[G/T]GGAGGCAAGAAAAAA | 8065 |
rs181540954 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108071091 | TTGTAAATTGAAAAA[G/T]TATTTATGAATACAG | 8065 |
rs181559771 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, synonymous-codon | CUL5 | GRCh38.p7 | 11:108106239 | TATTTGCTTGTCCCA[A/G]TACAAGAATGCCAAA | 8065 |
rs181573650 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108038982 | AGATTGTTCTGCATG[C/T]TGTGCAATATTTATC | 8065 |
rs181585954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108055759 | CCTCAGCCTCCCAAG[C/T]AGCTGGGACTACAAG | 8065 |
rs181588949 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108039349 | AACTCCAGTCATGAA[C/T]ACTCCTTCTGTGTCT | 8065 |
rs181597598 | snp | A/G | 0.000456779 | 0.0151057 | intron-variant | CUL5 | GRCh38.p7 | 11:108072501 | GATAGATATATATCA[A/G]GGCTATTTTTTAAAT | 8065 |
rs181604711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102247 | GTTGGCCGGGCTGAT[C/G]TCGAACTCCTGACTT | 8065 |
rs181609966 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108022190 | TGTTTCTATAATTTG[A/T]TGTGGTATGTTTTGT | 8065 |
rs181620545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017046 | ATCTGTGTAGCTGTG[G/T]TTTGTTCATTCCATA | 8065 |
rs181717468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108067006 | TCACTAAGTATGTAC[A/T]TGCTCTACTTCTGTA | 8065 |
rs181764154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084057 | GCCCAAGACAGTCCT[C/T]CTTCCAGTGTGGCCC | 8065 |
rs181863930 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052032 | GTGGAATAGTGTGAT[C/T]TTGGCTTGCTGCAGC | 8065 |
rs181875618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108086794 | TTACTGTGGTGCTTT[A/G]CCTCAGAATGTAGCA | 8065 |
rs181960162 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108076755 | TGCTGGGATTATGAT[G/T]ACATTATGAAGATAG | 8065 |
rs181961835 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108052259 | TAGACCACACGCAGT[C/T]GACCCTTCTTTACCA | 8065 |
rs181968215 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037381 | CATGAGTCCAACTTC[A/T]AACACCAGCTGTGTT | 8065 |
rs181968449 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095866 | TTTGGAAGGCCGAGG[A/T]GGGCAGATCACTTGA | 8065 |
rs181969617 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090841 | TATAGCTAGCCCTTC[G/T]CATGGAACTTTAGGA | 8065 |
rs181997824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018273 | TGTGGCTGGAACATA[C/G]AATTGCAGTAGTAAG | 8065 |
rs182000249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108058824 | GATCTGATTTTACAT[A/G]CAATTCTAATAAGCT | 8065 |
rs182004000 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108064008 | CTTCCTTTCCAATTT[A/G]GATGCTCTTTCTTTC | 8065 |
rs182161829 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108049590 | TCAAGCAATCCTCCC[A/G]CCTCAGCCTCCCAAA | 8065 |
rs182198186 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033068 | AAAGCTGTTGTACCC[A/G]TAGTTATGATTTGTT | 8065 |
rs182203432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108013024 | TAATGATATGGCTTA[C/T]TCTTCTCTCCCACCC | 8065 |
rs182211741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108088038 | TTGCTTAGGAAGAAT[A/T]CATTTATAGTTTTTT | 8065 |
rs182217610 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107635 | GATGATAATGCTGTA[A/C]AATTTTAAGTGGTAG | 8065 |
rs182231847 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108037769 | AAGGAAGTGTTCAAC[A/G]TAAGTCACACTGTTT | 8065 |
rs182233625 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108029113 | AGGTATTCCCCCATT[A/G]TCAACTCCCTGTTGG | 8065 |
rs182237993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069123 | TTAACCAGACTTGAT[A/G]GTACATCCCTGTAGT | 8065 |
rs182241012 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CUL5 | GRCh38.p7 | 11:108053021 | CATGCCATTAATTTC[C/T]TGGCAAGTCGTTTTA | 8065 |
rs182241311 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008077 | TAGGCGTGAGCCACT[A/G]CGCCCGGCCTCTTTG | 8065 |
rs182242414 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108075211 | TTTTTTTTTTTAATG[C/G]AAGTAGCTTATTTGG | 8065 |
rs182247309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108093198 | GTTTGAATAGCTTTT[A/G]CCTTCTTGTGTAACT | 8065 |
rs182249650 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CUL5 | GRCh38.p7 | 11:108026946 | GTGAGCAGAGATCAC[A/G]CCACTGCACTCCAGC | 8065 |
rs182272508 | snp | G/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107235 | ATGAAATGTTAGCTT[G/T]CTTTCTTTTACTTTT | 8065 |
rs182404994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084812 | AATAAAAAGGACAGA[A/T]ATAACACGTGTTGGT | 8065 |
rs182414625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102917 | CCTCTTTCTTCAGCC[G/T]CCTGAATAGCGGGGA | 8065 |
rs182427823 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108050430 | GGAGTGTGCAGTGGC[G/T]CAGTCTGCTCACTGC | 8065 |
rs182431839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034432 | AGTGAGCCACTGTTA[C/T]TTCAGGAAAGTGTAG | 8065 |
rs182439475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064933 | TGATATTAGTTCTAC[C/T]TGAAATATTTGGTAG | 8065 |
rs182501160 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108068237 | TGTATTATTTTCTTA[C/G]GACAGAAATATACAT | 8065 |
rs182508821 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102600 | CCTCCCAAATTGCTG[A/G]GATTGCAGGCATGAG | 8065 |
rs182516068 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108044536 | TTAGAATATAAAACA[A/G]TTTGATTATTGACAT | 8065 |
rs182538917 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108064157 | GTATGATACTAGCTA[C/T]GGGTCTCTCATGTGG | 8065 |
rs182540889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042830 | TGCAGAAGTGCAGTC[G/T]TCGCTCACTGCAACC | 8065 |
rs182586556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108046167 | GACACCATTTACTTG[G/T]TTCTAATATGGCCCA | 8065 |
rs182594568 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108080075 | TGTTTTAATTCCCGT[C/T]TCCCTCATGACTCTT | 8065 |
rs182637241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018726 | ACTTAATGTGGCACC[C/T]GCACACATTTATTTT | 8065 |
rs182770379 | snp | A/C/T | 0.0333695 | 0.124785 | intron-variant | CUL5 | GRCh38.p7 | 11:108058187 | ACACTCCAGCCTGGG[A/C/T]GATAGAGCAAGACTC | 8065 |
rs182821626 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108084218 | AACTAGAAAATCAGG[G/T]AAATGTAAAAAATAG | 8065 |
rs182859523 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108091209 | GGTTTGTGCCATGAC[A/G]CCTGGCTAATTTTTG | 8065 |
rs182869914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108060708 | CGGGCATGGTGGTGC[A/G]TGCCTGTAATCTCAG | 8065 |
rs182991468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059759 | CGTGGTGGCACGCAC[C/G]TGTAATCTCAGCTAC | 8065 |
rs183012034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108078975 | ATATATTTTAGAAGG[C/G]AATATGTTCTCTTTT | 8065 |
rs183013657 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108098117 | GCAATAACACTGAAT[C/T]CTAACCCATATATCT | 8065 |
rs183021085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028240 | CACAAGCTTTCCTTA[A/G]TAAGCCTGTCAAATC | 8065 |
rs183028808 | snp | A/G | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007037 | TTCAGTATGGGTAGC[A/G]TTAAACTTCAAATTT | 8065 |
rs183030502 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | CUL5 | GRCh38.p7 | 11:108099907 | TAAACAAAAAAAAAA[A/T]TTTTTTTTTTTTTTA | 8065 |
rs183031616 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108045102 | ATTTTCTGAACATGC[A/T]GTACTAGTATTAAAT | 8065 |
rs183042886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108057826 | GTTTTGATAGTTGTA[C/T]TATAGTTATGTAAGA | 8065 |
rs183044430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108074599 | CACCTGAGGTCGGGA[A/G]TTCGAGATCAGCCTG | 8065 |
rs183056599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108092222 | ACAAATGCTAGTAAG[A/G]AAGAGGAGAAATTGG | 8065 |
rs183057393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024322 | TGGGAGGCTGAGGCA[G/T]GAGGGCCACTTGATC | 8065 |
rs183075796 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108041289 | TTCTGTTTTTTCTTT[A/T]TTTTTTTTTTGAGAC | 8065 |
rs183116950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023852 | AAAGGAACCTAAAAG[C/T]TTAAACAGAGTGTGG | 8065 |
rs183125601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108057332 | GGCACTTGGCAGTAA[C/T]GGTCAAAAGTTTGAA | 8065 |
rs183150517 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074275 | TCTTGGCTCACTGCA[A/C]CTTCTGCCTCCCAGG | 8065 |
rs183258851 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108099695 | CAATTAAGATACAGA[A/G]CATTTGTGTCACACC | 8065 |
rs183285401 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CUL5 | GRCh38.p7 | 11:108079649 | AAATCTTAAGTGTAC[A/G]TTTGAGTCAGATTTG | 8065 |
rs183352985 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069391 | GCCTTCTCTTCCACT[C/G]TCTGTTTCTTCTCTA | 8065 |
rs183381043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037995 | GCTATTGTAATCGTT[C/T]TCTCTCTTTATCACT | 8065 |
rs183383869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108013441 | TTTGAGATCTTTCCA[A/G]CTGGGTCTTCTCCTG | 8065 |
rs183387745 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108040709 | AAGATCCTTGAGCAC[A/G]GGAGTTTTAAGTTAC | 8065 |
rs183468270 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108048729 | TGCAGTGCAGTAGCG[C/T]GATCTCGGCTCACTA | 8065 |
rs183487264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012080 | TTAGGGGTTTTGTAT[C/T]TCTGAAAACCTTTCC | 8065 |
rs183596901 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108088758 | TCAATTTAAAAATGT[A/G]TTATCTGTAAAGAAC | 8065 |
rs183617382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108019305 | GGGATTGGCAAATGG[A/G]GTTTTAAAATCACAT | 8065 |
rs183628583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108053721 | GTTTTGCTCTGTTGC[C/T]CAAGCTGGAGTGCAG | 8065 |
rs183694013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066190 | CTAAAAATACAAAAA[C/G]AAACTTAGCCAGGCG | 8065 |
rs183721130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015886 | GAAGGTAGAAAGAGG[A/G]TACTAGGCATCTTTC | 8065 |
rs183727762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108051703 | TTTTATAAGGTCCAG[C/T]ATCAGATTTTCAGTT | 8065 |
rs183732079 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108036260 | CATCCATTGTGGAGA[C/T]TTATTCTGCTCCCAA | 8065 |
rs183733487 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108060089 | GCTGAATAAGCAACT[A/G]GGTCACAAGTTATAA | 8065 |
rs183737491 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032357 | ACAAAAAAATACAAC[A/G]ATTAGCTGGGCATGG | 8065 |
rs183936787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108045541 | AGTGAGCTATGGTTG[C/T]GGCACTGCACTCCAG | 8065 |
rs183961591 | snp | A/G | 3.36973e-05 | 0.00410457 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054933 | ATTTAGAAACAAGAC[A/G]AGAATGTAACTCCGT | 8065 |
rs183966450 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070771 | TGTTTTTTAAATAAC[A/G]TACTTCTACTGAGTT | 8065 |
rs183971731 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108090285 | CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 8065 |
rs183971995 | snp | A/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105312 | AAAAACAACACAGAA[A/T]TCTCCTGCTCTGATA | 8065 |
rs184003870 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108051802 | ATCTGAAATTCAACC[A/G]TGGAACTATAGGAGA | 8065 |
rs184004049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066655 | TCCCGTGGTAACTAT[G/T]GTTTCTACCACTAGG | 8065 |
rs184013068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108086248 | AGCTTACAACTGAAA[A/G]CAATAATAAAACTTT | 8065 |
rs184022720 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108028609 | TTTCGGAGGCCGAAG[C/T]GGGCGGATCACAAGG | 8065 |
rs184156612 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007552 | GAAGTCAGAGTTGTA[C/G]CAGTGGTGTTTCCAG | 8065 |
rs184244610 | snp | A/C/G/T | 0.01193 | 0.0765113 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104480 | GGTTTATTTGGACTT[A/C/G/T]GATTACATAAATATT | 8065 |
rs184253596 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | CUL5 | GRCh38.p7 | 11:108081238 | GGTCGCAGTGAGCCG[A/C]GATCGTGCCATTACA | 8065 |
rs184259114 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108100151 | GAAACTTAAAAAAAT[A/T]AAAAAAAGGTGGTAG | 8065 |
rs184273642 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108046833 | CTGTTATGTATAAAT[A/C]AAAAATTTTGATCAA | 8065 |
rs184278091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108029504 | GTCAGTCAGTGAAAA[C/T]GTACATAAATCAAGG | 8065 |
rs184281237 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108061201 | CTTATCACTATACTT[A/T]CCATTCAAGATGTAT | 8065 |
rs184306693 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008451 | TGAAGGGGTAAAACC[C/T]GGAGGCTTATGGTTT | 8065 |
rs184349638 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108026729 | GGCGCAGTGGCTCAC[A/G]TTTGTAATCCCAGCA | 8065 |
rs184351751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108020681 | GCCACTGTGCCTGGC[C/T]TTGTGTTTGTGTTTC | 8065 |
rs184380470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085962 | ATGGTTTGCGAATTA[C/T]ATATCAGTAATTATT | 8065 |
rs184442878 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108025603 | GTGTTTCCACTCTGG[C/G]TGGTAGCAACACTAA | 8065 |
rs184470954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108076322 | TACAGGCATGAGCCA[C/G]CATGCCCAGCCCAGT | 8065 |
rs184472574 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108095368 | AAGCTGGGAGATGAG[C/T]GTGTATTCTGGGCAG | 8065 |
rs184489986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108044408 | TGGTCCCAGCTAGTC[A/G]GGAGGCTGAGGCAGG | 8065 |
rs184492534 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108038638 | CAAGATTGCACCATT[C/G]CACTCCAGCCTGGGA | 8065 |
rs184505261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108058599 | AATACTATAGAGTGT[A/G]TTGGTGGTGGTAATG | 8065 |
rs184508790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108082360 | ATCATGGCTCACTGC[A/G]GTGTTGCCCTCCTGA | 8065 |
rs184578859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108093834 | TCCGAGTAGCTGGGA[C/T]TATCTCGGCAGTATG | 8065 |
rs184605359 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | CUL5 | GRCh38.p7 | 11:108058499 | GTGATCTGCCCGCGG[C/T]GGCCTCCCAAAGTGC | 8065 |
rs184620914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108036985 | TATCTAAAGCTTTGC[C/T]CCAGCCCTGGGCTCT | 8065 |
rs184651216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100792 | TCCCAACACTTTGGG[A/T]GGCCGAGGCGGGTGG | 8065 |
rs184741917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108043879 | ACTGAAAATAAAAAA[A/G]TTAGCCAGTGGTGCA | 8065 |
rs184743772 | snp | C/G | | | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108108184 | GTGGGTGGATCACCT[C/G]AGGACAGGAGTTCAA | 8065 |
rs184755140 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108075982 | GAGCACCCAAAGTCT[A/C/G]CTTAGCATGAATCCA | 8065 |
rs184770948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108069893 | AGAGAGTCTAGTTCT[A/G]TAGTTTTTTTCCTTA | 8065 |
rs184786135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108019862 | CAGTTCTGTAGGCTG[A/G]TGAGGTCCTCAGCCT | 8065 |
rs184802733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108054256 | TGCAATCCACTTAGA[C/T]AACCTAGTCATATTT | 8065 |
rs184809152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038195 | TTTTATGAATGATAT[A/G]TTGGGTGTGGTGGGG | 8065 |
rs184963695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090639 | TTTAAATGATGGCCT[A/G]TTTAGGGTAATCAAT | 8065 |
rs184998287 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108018454 | GGCGGATCATGTGAG[A/G]TCAGGAGTTCAAGAC | 8065 |
rs185078708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039082 | CTGGAGTGCAATGGC[A/G]CAATCTCGGCTCACT | 8065 |
rs185084742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108071291 | TTTGAGACTGGGTCT[C/T]GCTGTGTTGCCCAAC | 8065 |
rs185194544 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108051364 | TTTTGGATTCAAATC[C/G/T]CAGTGTTGCCACTGA | 8065 |
rs185203248 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108091204 | CTACAGGTTTGTGCC[A/G]TGACGCCTGGCTAAT | 8065 |
rs185210616 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013772 | TGTAAAGCAGTGATT[C/T]AGAGTGTCTATAGAG | 8065 |
rs185233534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021742 | GCTAGTTTCAAACTC[A/G]TGGCCTCAAGTGATT | 8065 |
rs185286104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108035661 | GGGAGGATTGCTTGA[C/G]CCCTCAAGCAGATTG | 8065 |
rs185348656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085196 | ATATCCATTAGTTGC[A/G]TAGATAAGCAAAGTA | 8065 |
rs185407668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100606 | GAAGAATTTATACAA[C/T]AAAGGAAATAATTTC | 8065 |
rs185419578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108030658 | CAAAAAGAAAAAAGA[A/G]TACAGTGTGATAGAA | 8065 |
rs185422062 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108089119 | AAAAAAATAAGATAT[A/T]GGGCAAGTGTAGACA | 8065 |
rs185427518 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061611 | CTTCTGTTTGTTTTC[C/T]TTTCTTTTCCATTCC | 8065 |
rs185468085 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108065150 | CCTGCCTCAGCCTCC[C/T]AAGTAGCTGGGACTA | 8065 |
rs185477791 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108103213 | AGTAATTAAGGAAAT[A/C/T]ATCAAGAAAAATTTT | 8065 |
rs185490577 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031301 | CCCTGGGAGGTAGAG[G/T]CTATAGTGAGCCAAG | 8065 |
rs185496093 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010862 | TCAGCTCTTTGAGAG[G/T]CCAAGGTGGGAGGAT | 8065 |
rs185498210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048191 | TGTTAGGAAGGACCA[A/G]ATCTCCCAGATGGTT | 8065 |
rs185523174 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108081850 | TGCTGGTGCCACATC[A/G]TTGTGATTTACTGTA | 8065 |
rs185533027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108027911 | TTTGTCCAGAATACC[A/G]TACTCTTGGTTTTCT | 8065 |
rs185555565 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108044750 | TTTTACTTTTTTTTT[A/T]ATATTTTAATTTATT | 8065 |
rs185558061 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108047835 | ATAAATTATGTTTAT[G/T]TCAGATAGATAGAGC | 8065 |
rs185573502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108009606 | AAAAGCCTGGCTGAG[C/T]GCTGGCGAGGAGCGA | 8065 |
rs185752853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108101694 | TATTTCCCTCATACT[A/G]TGCTACTCTTTAAGT | 8065 |
rs185783779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108063175 | TTTGTACCCATTAAC[C/T]ATCCCTATTTCTCCC | 8065 |
rs185786100 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108082783 | GGACTAAGGGCCATA[C/T]CACCATGCCCGGCTA | 8065 |
rs185860042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108044625 | TCCATTATGAATTGA[A/G]TGAATCACTGGGGAA | 8065 |
rs185995661 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108027300 | TTTCTTTGAGACAGT[C/G]TCCCCCTGCTGTCCA | 8065 |
rs186006317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108058865 | TCGCTGGGCCTATAG[C/T]AGATGAACAGAAATG | 8065 |
rs186014850 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048456 | CATATATGGTTTTTG[A/C]TGTGGCTTTCTTTTC | 8065 |
rs186020854 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108031395 | ATCATGAGTTTCATA[A/G]GGTGTTTGGTGCTGG | 8065 |
rs186071112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090900 | TGCTTAGTAGGAAAA[A/T]GAATGATTATTCTGT | 8065 |
rs186097185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039626 | TACCCATTAAACAAT[A/G]ATTCTTCATTCTTCC | 8065 |
rs186103071 | snp | C/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108056362 | TTTTTACTTTTGACT[C/T]TTCTTTGGCTTTGTC | 8065 |
rs186105497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108072601 | TGGGGTATAAAGTTA[C/T]AGTTCAATAGGAAGA | 8065 |
rs186111117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023276 | ACAAAAAAAACGCAG[C/T]ATCTTCTCCACTCTG | 8065 |
rs186115213 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057100 | GTTAGTCATATCATA[G/T]CCACATTAAACTTAT | 8065 |
rs186123705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108022641 | AACACAGGACCCAAA[C/T]GCATTTTTAAAAATT | 8065 |
rs186158322 | snp | A/G | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108059598 | TATAAAATGGAATAG[A/G]CCGGGCGCGGTGGCT | 8065 |
rs186168658 | snp | G/T | 0.000792092 | 0.0198851 | missense | CUL5 | GRCh38.p7 | 11:108097743 | CTCAGTGAACCAGGA[G/T]TTCAGTTTAATGTAA | 8065 |
rs186213647 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108072940 | GGGCAAGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 8065 |
rs186214865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059835 | GTTGCAGTAAGGAGA[G/T]ATCACACCATTGCGC | 8065 |
rs186233598 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | CUL5 | GRCh38.p7 | 11:108079347 | CTGACCTCAAGTGAT[C/T]CGCCCACCTCAGCCT | 8065 |
rs186236336 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108062006 | AACCTTGCTGATCCA[A/G]TCACCTCCCACCAGG | 8065 |
rs186238274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108040439 | CAACATGGTAAAACC[C/G]TGTCTTTACTAAAAA | 8065 |
rs186239663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108098143 | TATCTTCAATTAGCT[A/T]GTCACTTTCATGGCA | 8065 |
rs186256291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108045208 | GATAGCTTTTGTTTT[C/T]GTTTTTTTGTTTAAA | 8065 |
rs186261226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028409 | GAACCACTTCTCATA[C/T]CTCCTACCTCCATTG | 8065 |
rs186304052 | snp | A/G | 0.00124629 | 0.0249318 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108078178 | TTATTTTTTGCAGGC[A/G]TATAAAGCAGTTGTT | 8065 |
rs186313165 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087523 | CTGCTGGGTGCAGTG[A/G]CATGCACCTGTAGTC | 8065 |
rs186349446 | snp | C/T | 3.32878e-05 | 0.00407956 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108052767 | GGGAGAAGCTTTTGA[C/T]TCTCAGCTGGTTATT | 8065 |
rs186351478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037543 | TGTGTGGCAAAGTCC[A/G]GGAGAAACGAAATCC | 8065 |
rs186358372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096090 | AACAGAGTGAGAACT[C/T]CGTCTGAAAAAAAAA | 8065 |
rs186359941 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016678 | TCTGTAAGGAAAGCA[A/G]GGCTGGGTGCAGTAA | 8065 |
rs186368549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108068985 | CCTTGGGGCCAGGCC[C/T]GATGGTTCACACCTG | 8065 |
rs186403602 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074297 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 8065 |
rs186620400 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108091277 | GCTGGTCTTGAAATC[C/T]TGGTCTTAAGTGATC | 8065 |
rs186650158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011418 | GAAAACTGCCTGAAT[A/G]TACAGAAAACGGGGT | 8065 |
rs186658549 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108057363 | ATGAAATAGGATATT[A/T]GCATAGTTTCAAAGT | 8065 |
rs186745963 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084297 | GAAATGTACAGAAAT[G/T]CCAGATAAACCTTTC | 8065 |
rs186766184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108049594 | GCAATCCTCCCGCCT[C/T]AGCCTCCCAAAGTGC | 8065 |
rs186771066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034272 | TCCAGCAATGATTGA[C/T]AGCGTGTGATATGTT | 8065 |
rs186803591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013131 | TTATCCTCTTTTCTG[A/G]TATTATTGCTCATTT | 8065 |
rs186842638 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108029276 | CCATTTGTGTGAGAA[C/G]AAGAGTGCCTGTGAA | 8065 |
rs186845489 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008078 | AGGCGTGAGCCACTG[A/C]GCCCGGCCTCTTTGC | 8065 |
rs186929417 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108052086 | TCCTCCCACCTCAGC[C/T]TCCCAAGTAGCTGGG | 8065 |
rs186977186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017186 | CTGAGCCCAGGAATT[G/T]TAGCCCACCCTGAAC | 8065 |
rs186988790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108046665 | TTTTGGCTACACATC[A/T]GTCCACACAGATCTT | 8065 |
rs186995394 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108069253 | TCCAGCTTGGGCAGC[A/G]GAGCAAGACTCTGTC | 8065 |
rs186996899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064025 | ATGCTCTTTCTTTCT[C/G]TTGTCTGATTCCTCT | 8065 |
rs187007900 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108088146 | AGTTTTAATATATTA[A/G]TCATAAAAAGTTTTA | 8065 |
rs187010870 | snp | C/G | 0.00199481 | 0.0315187 | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108107925 | CTTATTTATATTAGA[C/G]TTCAAATTCTAATTC | 8065 |
rs187010919 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060906 | CAGACCTATGAATTC[A/G]TTCATTCAACAGGTA | 8065 |
rs187012844 | snp | C/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032363 | AAATACAACAATTAG[C/G]TGGGCATGGTGGTGC | 8065 |
rs187044207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085041 | AAGAAGGTCAACAGA[A/G]TTGCTGTATGGCCCA | 8065 |
rs187046908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102944 | GGGACCACAGACACA[C/T]GCCACCATGCCTGGC | 8065 |
rs187077326 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050907 | TGAATATGAAGGGTC[C/T]TAGGTTTCCCTTTCA | 8065 |
rs187078835 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108065060 | AGACGGAGTCTTGCT[C/T]TGTCACCCAGGCTGG | 8065 |
rs187107213 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106385 | TGAGAGTCATGATGT[C/T]TTGATTTATGAAGGT | 8065 |
rs187129748 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007116 | ATTATTTTTTATAGC[A/G]ATAGCTACTTTGCAC | 8065 |
rs187136208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108067833 | TCCAGTGATGTTATA[A/G]AATAAGATTACTCAG | 8065 |
rs187164779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037196 | ATGGCCAGAAACTGC[C/T]AGGGGAATGAGGTAG | 8065 |
rs187165485 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CUL5 | GRCh38.p7 | 11:108102451 | CCTGACTCAGCCCCC[C/T]GCGTAGCTGGGACCA | 8065 |
rs187200720 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108048825 | GCGCATGCCACCATG[C/G]CTGGCTAATTTTTGT | 8065 |
rs187210637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084138 | TAGCATCCAAGTTAT[G/T]TGGGAGACTTGCTTC | 8065 |
rs187213595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012259 | GGCCCTTAGTGCTCA[C/T]TTTTTTCATTTCCAG | 8065 |
rs187249832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024021 | CACTAAATTTTTATA[A/G]TCATAGATCTTTGCA | 8065 |
rs187270587 | snp | C/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107454 | TGGGATGCTGTCTTA[C/T]GAATTCTTCCAAGGT | 8065 |
rs187278511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100227 | TAGTAATAAAACAGT[A/T]TGGCAAGAAGATTAA | 8065 |
rs187628999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108019560 | AAAAATTCCTATTGT[C/G]TGGCAATGTTTATTG | 8065 |
rs187687724 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108058275 | TTTTTTTGAAACATA[A/G]CCCTGATGTGTCACC | 8065 |
rs187691746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024809 | GTAGAAAATCTTGGA[A/G]TGGAATGATTAAACA | 8065 |
rs187700783 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108041444 | CACCGTGCTGGCCAA[C/T]TTTTGTATTTTTGGT | 8065 |
rs187723974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108025776 | TAGATACCCAGAGCT[A/C]CCTTGATGCCACAAA | 8065 |
rs187786660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037915 | GGATAGCAGTCTCAG[A/G]CACACTATTAAAATG | 8065 |
rs187872903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108058069 | CAAAAATTAGCCGGA[C/T]GTGGTGGCGTGCACC | 8065 |
rs187877209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108075101 | GAAGGAAGAAAGAAT[A/G]CCAGTTAAGAACTTA | 8065 |
rs187894375 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108092919 | CCACCCAGGTTCAAG[C/T]GATTTTCCTGCCTCA | 8065 |
rs187926088 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108054481 | TGCTTTATGCTGTTA[C/T]CTTTATAAGTTTCTT | 8065 |
rs187926258 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070639 | ATTTTTTTATTACTT[A/C]AATGTTTTCTTAAAA | 8065 |
rs187934199 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108089158 | GAGAGAGATGACTAG[A/T]GTCAGAAAAAAAAGT | 8065 |
rs187938829 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100047 | TTAATATCAAGTTCA[A/G/T]AATTTTAAAATTTCA | 8065 |
rs187943478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108019966 | AGTGGGGAGAGGTAC[C/T]AGGCTCTTTTTAACA | 8065 |
rs187968315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038469 | GAGGTGGGTGGATTA[C/T]CTGAGGTCAGGAGTT | 8065 |
rs187980166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108075448 | GTGCAGATACTAATA[A/G]TGGGAAAAGTATAAG | 8065 |
rs188007916 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108042834 | GAAGTGCAGTCTTCG[C/T]TCACTGCAACCTCCG | 8065 |
rs188073460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108013511 | CTCATACATGTGTGC[A/G]TACACACTCCTACTT | 8065 |
rs188075769 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108041140 | AGAACTGTGCTGATT[C/G]TTACTGCTCAAGCTT | 8065 |
rs188086534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108053371 | ACATAGAATGCATGG[C/T]ACAAAATCACTCTAG | 8065 |
rs188104425 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108018904 | TAGCTGTGTGGTATT[A/G]GGCAAGTTACTTAAC | 8065 |
rs188174472 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108066228 | GGATGCCTGCTGTCC[C/G]AGTACTCAGGAGGCT | 8065 |
rs188174573 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108086068 | AGAAAGTGTCTAAAA[C/G]CATATATAATTGGAG | 8065 |
rs188184640 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104592 | ACACTCTTTGACAGC[A/G]TGCTGTTTTGTGGAG | 8065 |
rs188260226 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108080758 | GAGTTCTTTATATAT[G/T]CTGGTACTGGATCCG | 8065 |
rs188323431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034793 | TCATGTCTTCTCAAT[C/G]ATCCAGACCTGCATG | 8065 |
rs188391176 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016089 | ACCCTAGGTCTGGCT[A/T]ATTTTTTATAGAGAT | 8065 |
rs188399274 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108051730 | AGTTGGTCCTTTTTA[A/C]ATTTTTTATGTGTCT | 8065 |
rs188401361 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108036302 | TTTAAATTCCAGTCC[C/T]TTCAGCAGAAAAAAG | 8065 |
rs188493755 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108088822 | CGGGGGGTTATTTTT[C/G]TTTCTGAAAATTTTT | 8065 |
rs188516246 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053740 | GCTGGAGTGCAGTGG[C/T]GTGATCATGGCTCAT | 8065 |
rs188579727 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108044019 | CAAGAGTGAAACTCC[A/G]TCTCTAAATAAATAA | 8065 |
rs188587352 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058527 | TGCTGGGATTACAGA[C/T]GTGAGCCACTGCACC | 8065 |
rs188604515 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108062089 | TACAGAGCCAAAGCA[C/T]ATCACAATCTATATT | 8065 |
rs188607773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108026479 | CTTCTCAGAGTCGTA[C/T]GACATCTATCCTTGT | 8065 |
rs188619475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108082387 | CTGAGCTCGAGTAAT[A/C]CTCCCACCTCAGCCA | 8065 |
rs188631898 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108031318 | TATAGTGAGCCAAGA[G/T]TATGCCACTGCACTC | 8065 |
rs188636128 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010863 | CAGCTCTTTGAGAGG[C/T]CAAGGTGGGAGGATT | 8065 |
rs188644356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048264 | AACAAAAAAAAAAGT[A/G]AAAATAATAAACATA | 8065 |
rs188648551 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090358 | ACGAGGCGTGGTGGT[A/C/G]GGGGGCCTGTAGTCC | 8065 |
rs188700510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108086696 | CCACCCTGTGATGGA[A/C]GTATCACAGCAGTTT | 8065 |
rs188730150 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108065883 | TGGCCATCTTGCTCC[A/G]CTCCTCTATTTTTTA | 8065 |
rs188746980 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108103916 | TGCACCCATCAACCC[A/G]TCATCTACATGAGGT | 8065 |
rs188758577 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108069420 | TACCATTTTAAGCTT[C/T]CTGGTATTCCTAGAA | 8065 |
rs188788875 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108038036 | TAATTTCCGAAATGA[A/T]GTAGGACCTTGCTGC | 8065 |
rs188816264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108081746 | GAGAGTGCGAGTCTC[C/T]GTCTCAAGAAAAAAA | 8065 |
rs188825046 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108039207 | TTGTATTTAGTAGAG[A/G]TGGGGTTTCTTCATG | 8065 |
rs188834201 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108045624 | TTCCAGCACTTTGGA[A/G]ACTGAGGCAGGAGGA | 8065 |
rs188849510 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108079880 | GCTTCTTTCATTCTG[C/T]ATTGTGTTTTTGAAA | 8065 |
rs188851612 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007853 | TCACTGCAATCTCCA[C/T]CTTCAGGGTTCAAGC | 8065 |
rs188854772 | snp | C/G | 0.00795532 | 0.062565 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105852 | AATGGAGTACAGAAA[C/G]GCATACAGTATTATG | 8065 |
rs189013378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085693 | AAAGAAGTGGGTCAC[A/C]AAATACCACTTATTG | 8065 |
rs189036373 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108096092 | CAGAGTGAGAACTCC[A/G]TCTGAAAAAAAAAAA | 8065 |
rs189039976 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047285 | TCATGCCATTGCACT[C/G]AGCTTGGGCAGCAGA | 8065 |
rs189043710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108051578 | TTGTTGCTGTCATTA[A/T]TGTATCTCCTACATC | 8065 |
rs189056510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021773 | GTCCTGCCTTGACCT[C/T]CCACAGTAATGGGAT | 8065 |
rs189058446 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061508 | ATATTTACACAAGTA[C/G]AGAAAATACTATAAT | 8065 |
rs189058755 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027357 | GCTCACTGCAAACTC[C/T]GCCTCCCAGGTTCAA | 8065 |
rs189068927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059024 | TTGTGTTTTAAGAGG[C/T]AGAGTCTCGCTATGT | 8065 |
rs189080480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099826 | ACCAGACAGTATGTA[C/T]TTTTATGTCTGACTT | 8065 |
rs189112196 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108060523 | AGGTAGAAATAATTA[G/T]GCAAATTGAATACCA | 8065 |
rs189257993 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108076472 | TGCCACTGGTACTAC[G/T]CTTTCATTCCTCTTT | 8065 |
rs189261929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095475 | TTCATGTCATAGATA[C/T]TAAGAGAGAATCATC | 8065 |
rs189277044 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108044523 | AAAAAAAAAAAAATT[A/G]GAATATAAAACAATT | 8065 |
rs189283450 | snp | A/G/T | 0.00716625 | 0.0594738 | intron-variant | CUL5 | GRCh38.p7 | 11:108026766 | GAGGCTGAGGTGGGC[A/G/T]GATCACGAGGTCAGG | 8065 |
rs189289165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108058794 | CTTATAGGAGAGCCA[C/T]TTAGACCCTACTTAG | 8065 |
rs189318012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108076919 | TTTGGAGAGATGGTT[A/G]CAGAGAGATCAGAAA | 8065 |
rs189343870 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108072785 | TATAGTATATACATG[C/G]ATTGAAATATAACAT | 8065 |
rs189350752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108044643 | AATCACTGGGGAACA[C/T]TTTTTGAATGAATGA | 8065 |
rs189506621 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108091084 | GGAGATGTAGTCTTG[C/T]TGTGTTACCCAGGCT | 8065 |
rs189520764 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108101235 | CATAGGTGGCATCTG[A/G]ATATATTGAGTGTGA | 8065 |
rs189537048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071026 | TAATCAGTACCGTGA[C/G]GTAGGGTTTTTGTGA | 8065 |
rs189547016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087833 | AGCCGGGCATGGTGG[C/T]GGGCACCTGTAATCC | 8065 |
rs189557116 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107590 | CTCATATGGTCTATA[C/T]GATTTTGAATGTGTG | 8065 |
rs189563318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038970 | GGGTGGTATAAGAGA[C/T]TGTTCTGCATGTTGT | 8065 |
rs189579979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037565 | ACGAAATCCAAACTT[C/G]CAAATGTCTTCTCGC | 8065 |
rs189581502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108051940 | GGGATTCAAATCCAG[C/T]TGGATTCTGAAACAC | 8065 |
rs189587327 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108052945 | TTTTGAGAGTAAGCA[A/G]ATGATAATTCTGCTT | 8065 |
rs189591329 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108069107 | AGAAAAGTTTAAAAA[A/G]TTAACCAGACTTGAT | 8065 |
rs189598490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108016925 | AGGCCAGGAGTTGGA[A/G]ACTAGATTGGGCAGC | 8065 |
rs189604875 | snp | A/T | 0.00359424 | 0.0422398 | intron-variant | CUL5 | GRCh38.p7 | 11:108018683 | GTGTCTTAAAAAAAA[A/T]AGAGAGAGAGAAACA | 8065 |
rs189631008 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108076063 | AGACAGAGTCTTGCT[C/T]TGTCACCCAGGCTGG | 8065 |
rs189787942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084322 | CCTTTCAGAGGTTAC[C/T]TGAGGATTTGTAACT | 8065 |
rs189796770 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108102828 | GCCTTTTGTTTTGGA[C/G]ACAGGGTCTCAGGCT | 8065 |
rs189841298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090675 | TTATAACTAAATTCC[C/T]ATATAAAGTATTTTG | 8065 |
rs189841515 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108020844 | AAGTGTTTATAAAGT[G/T]TACAGTAATGTCCTA | 8065 |
rs189851887 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066850 | TCTTTTCATACACAT[C/G/T]TGTACATATGAACCA | 8065 |
rs189873433 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108055630 | ATATATATATATATA[C/T]ACTTTATCTTTTTTT | 8065 |
rs189884593 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108037101 | ACTTTTGGGCCTCTT[C/T]CCACCTGGAGGCAAG | 8065 |
rs190031510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108064620 | GAGGCTAAGGCAGGA[A/G]AGTTGCTTGAACTTG | 8065 |
rs190094405 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029678 | TTTTTGGAATCTATT[A/G]TAAAAGTTTAATAGA | 8065 |
rs190142333 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108071528 | AAAGAAAGGAGTTGG[A/G]TTTTGCAGTATTTGA | 8065 |
rs190251434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108027925 | CATACTCTTGGTTTT[C/G]TTGCCACCTGTGCTC | 8065 |
rs190255571 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108006686 | CTGAAGTGCAGTGGC[A/G]CAATCTTGGCTCACT | 8065 |
rs190257801 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CUL5 | GRCh38.p7 | 11:108044843 | CTTGGCTCACTGCAA[C/T]CTCCGCCTCCCGGGT | 8065 |
rs190365106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108035948 | TTTGGCAGCAGTAAA[A/G]CCAAGATACTGCAGG | 8065 |
rs190378877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108009440 | CTTTGGGAAAGGCAC[A/G]GCTCAGGTTCAGCTG | 8065 |
rs190395152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108082008 | TGAAAAAGACCTTTG[A/G]AATTTTGATAGGAAA | 8065 |
rs190423606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059659 | CGAGATGGGTGGATC[A/T]TGAGGTCAGGAGTTC | 8065 |
rs190428680 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108078684 | ACAACTGGAATCTGA[A/G]CTAGTTATAGCACTT | 8065 |
rs190434172 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108047978 | GTAACATGACTGAAT[A/C]AAGTCTGGAAATGTA | 8065 |
rs190451693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010599 | AGTAGCGCCTGTATC[A/T]TAGGAACATTGTGAA | 8065 |
rs190467140 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108102078 | CCAGGCTGGGGTGCA[A/G]TGGTGTGATCTTGGC | 8065 |
rs190471418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108057802 | TATCGTACCAATACT[A/G]TTTTCCTGGTTTTGA | 8065 |
rs190491402 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108024036 | ATCATAGATCTTTGC[A/G]GTTTACTCTCTAAGC | 8065 |
rs190496946 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108063688 | TAGTGCTGCAGTAAA[C/T]GTGGAAGTGCATCTA | 8065 |
rs190503666 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108083938 | GCTTTGAACGTGGCC[C/T]AACACACACATTTGT | 8065 |
rs190511728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108041150 | TGATTCTTACTGCTC[A/G]AGCTTCCTTTCTTGT | 8065 |
rs190623126 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108014961 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 8065 |
rs190642938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108061884 | GCAAGGCACATCTTA[C/T]GTGGCAGCAGGAGAG | 8065 |
rs190652954 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CUL5 | GRCh38.p7 | 11:108100686 | TTTTTCTGTTTGGAG[A/G]AAAAGTAAGAAGATA | 8065 |
rs190664773 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108030710 | GTATATTAACTTTTA[A/G]GATGAACTATGTTCG | 8065 |
rs190860002 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108037230 | ATTTTCCTGGTTTAG[A/G]GCTATCATTTTCAAA | 8065 |
rs190867596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017280 | TTTTAGTTCTAGCTA[A/C]TCAGGAAGCTGAGTT | 8065 |
rs190892899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039693 | TGCTTATCTAGATAA[C/T]TCATATAAATGGAAT | 8065 |
rs190906787 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108056384 | GGCTTTGTCCATCTT[A/G]AGTGGTAGTCGTGTT | 8065 |
rs190914715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108012898 | CACTGCACTCTGCCT[C/T]CTCATACAAACTTGT | 8065 |
rs190932354 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022794 | TGGTTCAAGACTACA[G/T]TGAGCAGTGATGGTG | 8065 |
rs190946955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059847 | AGAGATCACACCATT[A/G]CGCTCCAGCCTGGGT | 8065 |
rs190948045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108079471 | GGTTGCTTTATCAAA[C/T]ATGTTATCTCCTTAT | 8065 |
rs190954301 | snp | A/G | 0.000399281 | 0.0141238 | missense | CUL5 | GRCh38.p7 | 11:108098480 | CTACAGAAAGGATGA[A/G]AGAAGAAGAGAATGA | 8065 |
rs191083325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074080 | AATTGCTGTTAGTTT[C/T]TTCTCTTCTTTGACT | 8065 |
rs191110157 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040708 | AAAGATCCTTGAGCA[C/T]AGGAGTTTTAAGTTA | 8065 |
rs191136837 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008076 | ATAGGCGTGAGCCAC[C/T]GCGCCCGGCCTCTTT | 8065 |
rs191234479 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108070770 | TTGTTTTTTAAATAA[C/T]GTACTTCTACTGAGT | 8065 |
rs191236475 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108054534 | ATAATTATATGTTCT[C/G]TTGAGCATTGTTACC | 8065 |
rs191250495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108089676 | ATTACATCATTTATA[C/T]GTGTGCTTAAGTAAT | 8065 |
rs191265099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038590 | TGAGGCAGGATAATC[A/T]CTTGAATCCGGCAGG | 8065 |
rs191340355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108091208 | AGGTTTGTGCCATGA[C/T]GCCTGGCTAATTTTT | 8065 |
rs191341857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108088367 | TAAAAGTGAGTGCCT[C/T]CCTAAATTAGGCACC | 8065 |
rs191355058 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108023733 | AAATAAGTTTAAACT[C/G/T]TTCTGTCAGTTTTAT | 8065 |
rs191365720 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018964 | AATAGCAGTGATCTC[A/C]AAAAAACCTCAGAAA | 8065 |
rs191370845 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108057115 | GCCACATTAAACTTA[A/G/T]GAACTTTCAACTGTA | 8065 |
rs191381715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108053481 | ATCAAGCCTTTAGAT[C/T]TTCATTAGCAGTGCT | 8065 |
rs191419840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108091646 | TTGAACAGAGATCTT[A/G]CCACTGTACTCCTGC | 8065 |
rs191478969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031738 | TGTTCATCACAGCAC[C/T]GTTCACTCTAACAAA | 8065 |
rs191575156 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108069260 | TGGGCAGCAGAGCAA[C/G]ACTCTGTCTCTTAAA | 8065 |
rs191584752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034387 | CAAAATCAGTGTAAA[C/T]CATATTGTTTATATA | 8065 |
rs191599759 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108037991 | TTGGGCTATTGTAAT[C/T]GTTTTCTCTCTTTAT | 8065 |
rs191622927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108098068 | GTTTCGTTTTTGTTT[C/T]TGTTTTTGTTTTTGT | 8065 |
rs191625555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108013207 | CTCTCTCTCAAATCA[C/T]GTTTGTTTTTCACTG | 8065 |
rs191666715 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | CUL5 | GRCh38.p7 | 11:108074581 | AGGCCAGGGCGGGTG[A/G]ATCACCTGAGGTCGG | 8065 |
rs191690865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048725 | AGGCTGCAGTGCAGT[A/G]GCGCGATCTCGGCTC | 8065 |
rs191714316 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108011849 | GCTAGGATGGTCTCC[A/C]TCTCTTGACCTCATG | 8065 |
rs191816097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108080775 | TGGTACTGGATCCGT[A/G]TCAGATAGATGATGT | 8065 |
rs191826006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108100093 | AGGAATATTTTTGGA[A/G]TTTTACAAATTGTTT | 8065 |
rs191841127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108046726 | CAAGTTGACAGTAAT[G/T]TCTTCAATTCCAGAT | 8065 |
rs191851747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108060916 | AATTCATTCATTCAA[C/G]AGGTACTTATTGGAG | 8065 |
rs191872746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108029435 | CTATTCTGAATAGTA[A/G]TGAAAGAATTCAAGA | 8065 |
rs191874396 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008326 | TCTTACTTATTTCTA[C/T]GCATTATGGCCGTAT | 8065 |
rs191891906 | snp | A/G | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107022 | CAGAGTTTAAGAAGT[A/G]AAAATATAGAAAAAT | 8065 |
rs191892842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085049 | CAACAGAGTTGCTGT[A/G]TGGCCCAACTGTTCT | 8065 |
rs191892890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108044054 | ATAGTATCTGGCACA[C/T]GATAAGCAGTCAGGT | 8065 |
rs191897111 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | CUL5 | GRCh38.p7 | 11:108058543 | GTGAGCCACTGCACC[C/T]GGCCCAAAGTGATTT | 8065 |
rs191899326 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108103191 | TAACTCTTATTGTAA[A/G]CTTAACAGTAATTAA | 8065 |
rs191899663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108076107 | GCACAACATGGCTCA[C/T]TGGAGCTTCGACCCC | 8065 |
rs191910719 | snp | G/T | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007133 | TAGCTACTTTGCACA[G/T]GCTGGTCTCGAACCC | 8065 |
rs191915872 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | CUL5 | GRCh38.p7 | 11:108068159 | CTGACCTCAGGTGAT[C/T]CGCCCGCCTTAGCCT | 8065 |
rs191917683 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108045212 | GCTTTTGTTTTTGTT[C/T]TTTTGTTTAAAGGAG | 8065 |
rs192121882 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108048908 | ATGACCTCGTGATCT[G/T]CCCGCCTTAGCCTCC | 8065 |
rs192130414 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108084150 | TATTTGGGAGACTTG[C/T]TTCTGAGGAGGAGTG | 8065 |
rs192160640 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108100265 | AAATAACTTTAGGCT[C/T]GGCGCGGTGGCTCAC | 8065 |
rs192166258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108060630 | CACCTGAGGTCAGGA[A/G]TTCAAGACCAGCCTG | 8065 |
rs192189290 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108087247 | GGGAGGAAAAAAGTT[A/T]CATCCACCCCACTAA | 8065 |
rs192194364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108028988 | TACTTCTATGACCTT[A/G]TCTGCTCTCTCCACT | 8065 |
rs192211454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108052092 | CACCTCAGCCTCCCA[A/C]GTAGCTGGGACTACA | 8065 |
rs192232320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028582 | GGTGGATCACACCTG[C/T]AATCACAGCACTTTC | 8065 |
rs192310977 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032637 | ATCATTATTTTTCCT[A/G]ATATTGCACTACTTT | 8065 |
rs192398960 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108043360 | ATTACAGACATGAGC[C/T]AATATGCCTGGCCCA | 8065 |
rs192407542 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108075475 | TAAGGGATGTGGGAA[A/G]GTTTGACAGCATTTG | 8065 |
rs192455215 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108053919 | GTGCAGTGGCATGCT[C/T]GCTGCAACCTCCACT | 8065 |
rs192457852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108038086 | ACTTCTTGCCTTTGG[A/G]AAATTAAAGTTTAGT | 8065 |
rs192465224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102505 | CTAATTTGTTTTTGT[A/G]TATTTTGTAGAGATG | 8065 |
rs192504482 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108064151 | CATTCAGTATGATAC[C/T]AGCTACGGGTCTCTC | 8065 |
rs192549599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108020377 | GGTTGAAGACAGTGA[C/T]GATGATCCTGACCCT | 8065 |
rs192555853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108045750 | CCTATAGTACCAGCT[C/T]TTAGAAGGCTGAGGA | 8065 |
rs192574186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108079914 | TTTTATGTTTTGGCA[G/T]GTAACAGTAGTTTGC | 8065 |
rs192635824 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108058166 | GTGAGCCGAGATTGC[A/G]CCACCACACTCCAGC | 8065 |
rs192641504 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108035951 | GGCAGCAGTAAAGCC[A/G]AGATACTGCAGGCTC | 8065 |
rs192658892 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108015388 | CGAAGATTTGAATAT[C/G]ATCGGTGAATGTGGT | 8065 |
rs192664449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108075122 | TAAGAACTTATTTAA[A/C]TAATTCAATTAAGTG | 8065 |
rs192668362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108093149 | TTTATGGTAGATAAA[G/T]TATCTGACACAGTAA | 8065 |
rs192689170 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108042519 | GAGCCACTGCACCTG[A/G]CCCACAATTCTATAT | 8065 |
rs192743613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108093560 | TTTATATCTTTGCCA[A/G]TTATCTTGTTTGATT | 8065 |
rs192757284 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108058483 | TTGATCTCCTGACTT[C/T]GTGATCTGCCCGCGG | 8065 |
rs192777876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108090423 | TGAACCCTGGGGGGC[A/G]GAGCTTGCAGTGAGC | 8065 |
rs192817746 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034821 | ATGAGGGACAAAAGT[A/C]TTTTTCACTAAAAAA | 8065 |
rs192826235 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108065092 | GTGCAGTGGCATGAT[A/C]TCGGCTCACTGCAAG | 8065 |
rs192875133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108025962 | TTCTTTTCTCAGGAA[A/G]CGCTGTCCTGCACTG | 8065 |
rs192894598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095180 | ACTTAAGATACTGCC[A/G]TTGTCTACAGAATTC | 8065 |
rs192945936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069658 | GACAGTGATCTCTTC[A/G]AGAGCAGGAATTATA | 8065 |
rs192949432 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108047592 | GAGTAAGACTAATCT[A/G]TTGGATATTACTTAA | 8065 |
rs193034011 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CUL5 | GRCh38.p7 | 11:108051010 | AAAGTAAAAAATGCC[A/G]TTTGAACTTTAGTCA | 8065 |
rs193042385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013659 | GCAGTAGTATATAAC[C/T]GAACCACAAGATAAA | 8065 |
rs193061441 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108009543 | CGGGTCTGTGGCCTT[A/G]GGGTCGACAGGCTCT | 8065 |
rs193136055 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108085888 | TATGGTGATGATTAC[A/G]CAACCCTCTGAATAT | 8065 |
rs193141815 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108051683 | AAACAGTAGATTTGC[A/G]GACCTTTTATAAGGT | 8065 |
rs193151735 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108025381 | AGTATATGTTTTAGG[A/G]GCTTGATTTTAAAAT | 8065 |
rs193176295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030393 | CTGTAATCCTAGCAC[C/T]TTGGGAGGCTGACGT | 8065 |
rs193177761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108088960 | TGGAATGATAGTTGA[A/C]AGATTGGGAGTTTTT | 8065 |
rs193178562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108061589 | TGTCATGCTTGTTTT[A/G]TTGATCCTTCTGTTT | 8065 |
rs193285141 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108066138 | AAGGTCAGGAGATCA[A/G]GACCATCCTGGCTAA | 8065 |
rs193289172 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CUL5 | GRCh38.p7 | 11:108103924 | TCAACCCGTCATCTA[C/T]ATGAGGTGTTTCTCC | 8065 |
rs199562808 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CUL5 | GRCh38.p7 | 11:108054858 | CTTAAAATGATTGCT[A/G]TTTTGCTTCTGGACA | 8065 |
rs199582691 | in-del | -/ACTT | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108022582 | TTTCTGGCTGATAAC[-/ACTT]ACCCCCAGCCCAAAC | 8065 |
rs199589248 | in-del | -/AAGAG | 0.0170251 | 0.090679 | intron-variant | CUL5 | GRCh38.p7 | 11:108018683 | GTGTCTTAAAAAAAA[-/AAGAG]AGAGAGAAACATCAC | 8065 |
rs199596912 | snp | A/T | 3.36157e-05 | 0.0040996 | intron-variant | CUL5 | GRCh38.p7 | 11:108046227 | TGTTTTGTTCAGTTC[A/T]TGTTTCATTATTAAT | 8065 |
rs199665006 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020550 | ATTTTTTTTTTTTTG[G/T]TTTTTGTTTAAAATA | 8065 |
rs199710516 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063654 | ATAAAATTAATAAAA[-/T]TTAAAAAAAATAAAT | 8065 |
rs199749961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108016333 | GTACAGTGGCGCAGT[C/T]ACAGCTCCCTACAGC | 8065 |
rs199791913 | in-del | -/AG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023859 | CCTAAAAGTTTAAAC[-/AG]AGTGTGGTATGAAAT | 8065 |
rs199857275 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048119 | TAAACGCTTAAGAAA[-/T]TTTTTTTTTTTTTTC | 8065 |
rs199948513 | in-del | -/AATA | 0.0260105 | 0.111035 | intron-variant | CUL5 | GRCh38.p7 | 11:108055610 | TCACCCTGCCTGACT[-/AATA]AATATATATATATAT | 8065 |
rs199960553 | snp | C/T | 6.60142e-05 | 0.0057448 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108072372 | GGACAAAGTTCCTAA[C/T]GGTATAGAGCCAATG | 8065 |
rs199973906 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012525 | ATGTCCCCTCTTACT[C/T]TTTTTTTTTTTTTTT | 8065 |
rs199979499 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108074701 | ATTCCAGCTACTTAG[A/G]AGACTGAGGCAGGAG | 8065 |
rs200023147 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | CUL5 | GRCh38.p7 | 11:108100150 | GAAACTTAAAAAAAT[-/A]AAAAAAAAGGTGGTA | 8065 |
rs200068874 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083342 | GTTTCCGATGTGTTG[A/C]TATTACTGTTAGTGC | 8065 |
rs200079709 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067479 | ACAAAAGTCTTATGA[A/T]ATAATATTCATTGTT | 8065 |
rs200106578 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085705 | CACAAAATACCACTT[-/A]TTGTATGATAACATT | 8065 |
rs200133612 | in-del | -/TTTTT | 0.360632 | 0.224189 | intron-variant | CUL5 | GRCh38.p7 | 11:108042219 | AGTCATCCACAATTC[-/TTTTT]TTTTTTTTTTTTTTG | 8065 |
rs200152671 | snp | A/C | 0.000492793 | 0.0156893 | intron-variant | CUL5 | GRCh38.p7 | 11:108095519 | TTAAAAATCTGTTTT[A/C]TCTATTATAGATAAC | 8065 |
rs200244716 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080111 | TGAGCAATTTTTCAT[C/T]TTTTTTTTTTTTTTT | 8065 |
rs200263260 | snp | A/C | 1.8248e-05 | 0.00302054 | intron-variant | CUL5 | GRCh38.p7 | 11:108088682 | AATTTTTTGTATTTC[A/C]ACTTTTAAAATTACC | 8065 |
rs200271588 | in-del | -/TT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103446 | AAACATTTAATTGAG[-/TT]TCAATATAAACTGAA | 8065 |
rs200353945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108013741 | TTTTATCCTTTAAGA[A/G]GAAAGAAAATGGAAA | 8065 |
rs200385430 | snp | A/C | 0.00075242 | 0.0193815 | intron-variant | CUL5 | GRCh38.p7 | 11:108009411 | GTTTTACTGTGTGGC[A/C]GCCGGGTTCGGCTCT | 8065 |
rs200436493 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103412 | ATTTAAAGAGAAGAA[-/G]GGGAAAAAAAAAACC | 8065 |
rs200439754 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020546 | GTGATTTTTTTTTTT[-/G]TTGTTTTTTGTTTAA | 8065 |
rs200442415 | in-del | -/TAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063663 | TAAAATTTAAAAAAA[-/TAA]ATAAATAAATAGTGC | 8065 |
rs200474086 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103951 | CTCCTAATGCTTATC[C/G]CTCCCCTATCCCCCC | 8065 |
rs200531430 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066499 | AACTCACTCTGTTAC[-/T]TTTTTTTTTGGATTC | 8065 |
rs200546607 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100756 | TGAAATGTGGCCAGG[C/T]GCGGTGGCTCACGCC | 8065 |
rs200553598 | snp | A/C | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033802 | TTTTTTTTTTTCAAG[A/C]ATAAAGGTTCTCTTC | 8065 |
rs200597658 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018687 | CTTAAAAAAAAAAGA[C/T]AGAGAGAAACATCAC | 8065 |
rs200618012 | in-del | -/TAA | 0.0130921 | 0.0798413 | intron-variant | CUL5 | GRCh38.p7 | 11:108019734 | ATAAAATTATTATCC[-/TAA]TAATAATAAGTGACT | 8065 |
rs200626901 | snp | C/T | 0.0019981 | 0.0315446 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094489 | TTTTAAGGAAATGCA[C/T]AAAAATAATAAATTG | 8065 |
rs200639536 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108046678 | CAGTCCACACAGATC[-/T]TTTTTTTTTCTCTCA | 8065 |
rs200647271 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090039 | AGTGGGACTCCATTT[A/C]AAAAAAAAAAGAATA | 8065 |
rs200682671 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042218 | TAGTCATCCACAATT[C/T]TTTTTTTTTTTTTTT | 8065 |
rs200744514 | snp | A/G | 4.98757e-05 | 0.00499353 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108052674 | GCTTATGCTTGATAC[A/G]TGGAATGAGTCAATC | 8065 |
rs200763751 | in-del | -/TTTTTTTG | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007765 | GTAGTTTTTTTTTGT[-/TTTTTTTG]TTTTTTTTTTGAGAC | 8065 |
rs200802906 | snp | A/G | 0.000127132 | 0.00797182 | intron-variant | CUL5 | GRCh38.p7 | 11:108054623 | GATCATAATTGGAGT[A/G]ATACTTTATTTTCTG | 8065 |
rs200813419 | snp | A/T | 0.000131872 | 0.00811902 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108095655 | TCTTAAGCTTGCAAC[A/T]GAACTCCCTGATGCT | 8065 |
rs200850488 | snp | A/G | 1.6486e-05 | 0.00287102 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108070128 | AAATGCCCTGGTGAC[A/G]TCATTTAAAGAGACT | 8065 |
rs200918783 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080961 | ATTTATCATTATTTA[A/T]TTATTTATTTATTTA | 8065 |
rs200926051 | in-del | -/AAC | 0.0283406 | 0.115616 | intron-variant | CUL5 | GRCh38.p7 | 11:108072190 | TCTCAAAAACAAAAA[-/AAC]AACAACAAAAAAACG | 8065 |
rs200939610 | snp | G/T | 1.66189e-05 | 0.00288256 | intron-variant | CUL5 | GRCh38.p7 | 11:108097623 | CTAATTGTTTTCTCC[G/T]TATTCTTCATAGTCT | 8065 |
rs200968633 | snp | C/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106834 | AATCCAGCCTCCCCC[C/T]CCAAAAAAAAAAAAA | 8065 |
rs200991204 | in-del | -/TTTT | 0.0629771 | 0.165899 | intron-variant | CUL5 | GRCh38.p7 | 11:108048649 | ATAGACTCCACCACC[-/TTTT]TTTTTTTTTTTTTTT | 8065 |
rs200991955 | in-del | -/CTGATT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108054600 | ATTATACTCAAAATA[-/CTGATT]TTGATCATAATTGGA | 8065 |
rs201028665 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013791 | GTGTCTATAGAGGCC[A/G]GGCATGGTGGCTCAT | 8065 |
rs201205728 | snp | A/G | 0.00299555 | 0.038585 | intron-variant | CUL5 | GRCh38.p7 | 11:108018802 | TCCCCTATAGATGCA[A/G]GTAGTGTACTTGCAA | 8065 |
rs201286435 | snp | C/T | 0.000132941 | 0.00815187 | intron-variant | CUL5 | GRCh38.p7 | 11:108078259 | AGTTTTTTAAAACCA[C/T]ACTTTAAAAATACTT | 8065 |
rs201313802 | in-del | -/A | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106684 | ATTTAAAAAAAAATG[-/A]AAAAAAAAAATCTTA | 8065 |
rs201325114 | in-del | -/AAT | 0.0240976 | 0.107089 | intron-variant | CUL5 | GRCh38.p7 | 11:108024427 | AATCTTGTCTCAAAA[-/AAT]AATAATAATAATAAT | 8065 |
rs201340912 | in-del | -/ATAAA/TAAG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063664 | AAAATTTAAAAAAAA[-/ATAAA/TAAG]TAAATAAATAGTGCT | 8065 |
rs201378566 | snp | A/G | 0.000254046 | 0.0112676 | intron-variant | CUL5 | GRCh38.p7 | 11:108095016 | GTGTTAGTTATTTCA[A/G]CTTTCAGTTTGGATG | 8065 |
rs201399614 | in-del | -/GGCC | | | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008950 | GAACCTGAGCTGCGG[-/GGCC]TAAGCCGAGCTAAAT | 8065 |
rs201430106 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022098 | GATCCTCCCACCGTG[C/G]TGGAATTATAGGCAT | 8065 |
rs201442809 | snp | A/G | 5.15832e-05 | 0.00507828 | intron-variant | CUL5 | GRCh38.p7 | 11:108009415 | TACTGTGTGGCCGCC[A/G]GGTTCGGCTCTTTGG | 8065 |
rs201460345 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063654 | ATAAAATTAATAAAA[A/T]TTAAAAAAAATAAAT | 8065 |
rs201470793 | snp | A/G | 0.00255365 | 0.0356413 | intron-variant | CUL5 | GRCh38.p7 | 11:108049866 | ACTGCATTTATTTCA[A/G]ATTGGTACACCTCTT | 8065 |
rs201514951 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087975 | CATCTCAAAAAAACT[-/A]AAAAAAAATTTGTAT | 8065 |
rs201607835 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108063006 | ATGCACCACCACGCC[C/T]GGCTAATTTTGTATT | 8065 |
rs201629707 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020544 | TTGTGATTTTTTTTT[-/G]TTTTGTTTTTTGTTT | 8065 |
rs201661444 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020549 | GATTTTTTTTTTTTT[G/T]TTTTTTGTTTAAAAT | 8065 |
rs201663425 | in-del | -/T | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007753 | TTTTTTTGTTTGTAG[-/T]TTTTTTTTTGTTTTT | 8065 |
rs201696152 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067477 | AAACAAAAGTCTTAT[A/G]AAATAATATTCATTG | 8065 |
rs201707666 | snp | A/T | 0.000766146 | 0.0195573 | intron-variant | CUL5 | GRCh38.p7 | 11:108073519 | ATTCCTATATATATA[A/T]AAAACACTTTTAAAA | 8065 |
rs201774636 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080127 | TTTTTTTTTTTTTTT[C/T]CCGGTATTCGTATAT | 8065 |
rs201838611 | snp | A/G | 0.000231677 | 0.0107603 | synonymous-codon, intron-variant | CUL5 | GRCh38.p7 | 11:108104309 | AATGATAAAAGAGCA[A/G]ATAGAGTGGCTAATA | 8065 |
rs201907478 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020545 | TGTGATTTTTTTTTT[-/G]TTTGTTTTTTGTTTA | 8065 |
rs202007296 | in-del | -/AAAAT | 0.00755907 | 0.0610114 | intron-variant | CUL5 | GRCh38.p7 | 11:108090495 | GACTCCATCTCAAGA[-/AAAAT]AAAATAAATAAATAG | 8065 |
rs202082346 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086599 | ATACAGAAAGACTTC[C/T]CTAGAGCATGCCAGT | 8065 |
rs202086072 | snp | A/T | 8.32563e-05 | 0.00645145 | missense | CUL5 | GRCh38.p7 | 11:108094413 | GTATGCCAGCGGATT[A/T]TGTAAACAAGCTTGC | 8065 |
rs202118152 | snp | A/C | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106836 | TCCAGCCTCCCCCTC[A/C]AAAAAAAAAAAAAAA | 8065 |
rs202168252 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032601 | CTCTCTCTCTCTCTC[-/TT]TGTTTTTGGCAATGT | 8065 |
rs207472326 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047506 | GTTTTTTCTATGTAT[G/T]ACTTAAGATATTGAA | 8065 |
rs367555028 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043033 | CTCCCAAAATGCTAG[A/G]ATTAAAGGCATGAGC | 8065 |
rs367631054 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086898 | TTAGGTATCAGATCC[G/T]AGTCAGATAGTTTCT | 8065 |
rs367668594 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037695 | AACTTTCTACTGGGG[-/G]CTCGTCATGTAAGCA | 8065 |
rs367675992 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032787 | AGTTTCCATTTCTTA[C/T]GCTTTTCTCAGCAGT | 8065 |
rs367683942 | snp | A/G | 0.000115436 | 0.00759637 | missense | CUL5 | GRCh38.p7 | 11:108072409 | GACTTGGAGGAACAT[A/G]TCATTAGTGCTGGCC | 8065 |
rs367712018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039372 | CTGTGTCTTTCTCCT[C/T]ACCCTTCTGTGTCTT | 8065 |
rs367713492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108060552 | CACTAAAAGAAGAAT[C/G]TGGCTGGATGCCGTG | 8065 |
rs367730220 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022228 | GTTATGTAGGGATTT[C/T]TGGGTGTTTTCGGGG | 8065 |
rs367739050 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108093761 | TGCCCAGGCTGGAGC[A/G]CAGTGACACAATCAG | 8065 |
rs367753086 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108047563 | TAATTTTGCTAGTAG[A/C]CACTACCATGATGGA | 8065 |
rs367765329 | snp | C/T | 0.000395844 | 0.0140629 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108088560 | GCCTGAATCAAAATG[C/T]CCTGAGCTGCTTGCC | 8065 |
rs367766251 | snp | C/T | 1.66084e-05 | 0.00288165 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108072348 | ATTACATTTAATGTT[C/T]TCATTGATGGACAAA | 8065 |
rs367811912 | snp | A/G | 3.3588e-05 | 0.00409791 | intron-variant | CUL5 | GRCh38.p7 | 11:108097601 | TATTCCATACTGTTT[A/G]TAGATGCTAATTGTT | 8065 |
rs367871954 | in-del | -/GAAAT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067477 | AAACAAAAGTCTTAT[-/GAAAT]AATATTCATTGTTAC | 8065 |
rs367974623 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068280 | TTAAAAGTCATCAGC[A/G]TCATTCTTGTAGAGG | 8065 |
rs367980830 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089808 | ACTTTGGGAGGCCGA[A/G]GCAGGTGGATCACCT | 8065 |
rs367987153 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048331 | CTGTTTTATTTGTTC[A/G]CAATTCTGTGGCTTA | 8065 |
rs368207906 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108090836 | TAACTTATAGCTAGC[A/C]CTTCGCATGGAACTT | 8065 |
rs368249929 | snp | A/G/T | 8.95703e-05 | 0.00669164 | intron-variant | CUL5 | GRCh38.p7 | 11:108094778 | TTTTATCCATTGTTA[A/G/T]TTTACTTTATATTCC | 8065 |
rs368255549 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007989 | CAGGCTGGTCGCGGA[C/T]TCCTGACCGCAGGTG | 8065 |
rs368265467 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050176 | TCTACTTCACATGTC[A/G]ATTGCTTTTCAGCTC | 8065 |
rs368273361 | snp | A/G | 4.94645e-05 | 0.00497291 | missense | CUL5 | GRCh38.p7 | 11:108097694 | ATGAACCTCAAGTCA[A/G]CTCACCCAAAGACTT | 8065 |
rs368395752 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108054106 | CCACCTTGGCCTCCC[A/G]CAGTGCTGGGATTAC | 8065 |
rs368415973 | in-del | -/ATTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108021825 | CCAGTTTATTTATTT[-/ATTT]TTCAGAGACAGGGTC | 8065 |
rs368452724 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038677 | AAAACTCCATCTCAG[-/A]AAAAAAAAAAAAAAA | 8065 |
rs368503769 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108086276 | TTTTAAAACAGCCAC[A/G]GGGGAAAAATAACAC | 8065 |
rs368523747 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108073196 | GACAGATCGAGACTC[C/T]GTCTCAAAAAAAAAA | 8065 |
rs368526737 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031137 | CTTTGGAAGGCTGAG[A/G]AGGGTGGATCATATG | 8065 |
rs368556298 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011519 | GGAAGGTGATAATAT[C/T]TTGAAAAAAAGTAAG | 8065 |
rs368601660 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108081161 | GGCGTGGTGGCTCAT[G/T]CCTGTGATCCCAGCT | 8065 |
rs368641367 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056330 | ATTTTTCAACTCTGA[A/G]TGGGATTTAAAATTT | 8065 |
rs368652423 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058484 | TGATCTCCTGACTTC[A/G]TGATCTGCCCGCGGC | 8065 |
rs368681058 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108045301 | TGTGATTTAAGTGAC[C/T]AATTTTTTTAAAAAG | 8065 |
rs368696319 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075148 | AAGTGATGATGGAGG[C/T]TTGTCCCAGAGTGAT | 8065 |
rs368712400 | snp | A/G | 5.09109e-05 | 0.00504508 | intron-variant | CUL5 | GRCh38.p7 | 11:108046381 | GGCAGTAAGTTCTAC[A/G]TGCTTATTTTAGACT | 8065 |
rs368794124 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108062631 | TTGTATGTATTTATG[C/G]GTTACATGAGACATT | 8065 |
rs368851030 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108031808 | GATAAAGAAAATGTG[A/G]TACATATACACCATG | 8065 |
rs368892658 | snp | A/G | 0.000153988 | 0.00877328 | missense | CUL5 | GRCh38.p7 | 11:108098467 | CGTTTGCAGCTCACT[A/G]CAGAAAGGATGAGAG | 8065 |
rs368894731 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026271 | GAAAAAGACACAACC[A/G]TGCTATTTGCACCTT | 8065 |
rs368969520 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061980 | CCCTGTCACAAGAAC[A/G]GCATGGGGGAAACCT | 8065 |
rs368975766 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CUL5 | GRCh38.p7 | 11:108070211 | AAAACATCACATAAA[A/G]TTATCATAATCTTCT | 8065 |
rs368996301 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008701 | TCAACACATATTTAC[A/T]GGGCGCATTCTATGC | 8065 |
rs369068428 | snp | A/C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060730 | TAATCTCAGCTACTC[A/C/G]GGAGGCTGAGGCAGG | 8065 |
rs369076120 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017554 | AGCGAAAACAACGTG[A/G]TAAGAATGTTCAAGG | 8065 |
rs369122457 | snp | C/T | | | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074224 | TTTGAGACTGAGTTT[C/T]GCTCTTGTTGCCCAG | 8065 |
rs369166834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108051467 | TCATAGTACCTATAT[C/G]AAGATTATGAGGATT | 8065 |
rs369176858 | snp | A/C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014296 | GCAGTGTAAGCAGGG[A/C/T]TGCATGCTGTGTTAG | 8065 |
rs369202742 | in-del | -/ATCT | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108063699 | TAAACGTGGAAGTGC[-/ATCT]ATCTCTTCCTTTCTT | 8065 |
rs369259186 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108078743 | TTAGTTAAAAAAAGT[A/C]TTTTGATGTGCTTCT | 8065 |
rs369297599 | snp | C/T | 0.00011875 | 0.00770459 | intron-variant | CUL5 | GRCh38.p7 | 11:108052647 | ATGTTACAATTTGTT[C/T]TTGTTTTCCTAGCTT | 8065 |
rs369360610 | snp | A/G | 8.25219e-05 | 0.00642294 | intron-variant | CUL5 | GRCh38.p7 | 11:108055006 | ATTTGAAATACGGAA[A/G]CATAGGAATGGCAAA | 8065 |
rs369374506 | snp | A/C/G | 1.67891e-05 | 0.00289729 | intron-variant | CUL5 | GRCh38.p7 | 11:108094368 | TATTTATTACCTCTT[A/C/G]CTTCTTTGGTTTATA | 8065 |
rs369409611 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038737 | GCAGTTCAGTGTATC[A/G]TCCTTTTAGGTAAAG | 8065 |
rs369423071 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100784 | GCCTGTAATCCCAAC[A/G]CTTTGGGAGGCCGAG | 8065 |
rs369462426 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052390 | CGTGGTCTCGGCTCA[C/T]TGGGACTACAGGCGT | 8065 |
rs369519066 | in-del | -/TTTCT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016277 | TCTCTTCTCTTTTCT[-/TTTCT]GTTGAGACAGGGTCT | 8065 |
rs369527783 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018520 | AAAAAAAAAAAAATA[-/C]AAAAATTAGCTGAGT | 8065 |
rs369530222 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018697 | AAAGAGAGAGAGAAA[C/T]ATCACATATATGCAC | 8065 |
rs369539899 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108094609 | TCAGCAGTAATAGAT[A/C]GAAAGATGTTATGAA | 8065 |
rs369567236 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024500 | ATTAATTCATACTTG[C/T]AAAGTGTTTGGAACA | 8065 |
rs369568668 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | CUL5 | GRCh38.p7 | 11:108020544 | TTTGTGATTTTTTTT[G/T]TTTTGTTTTTTGTTT | 8065 |
rs369604779 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009633 | GCGATGCTTTCAAGG[C/G]ACCAGCTCTGGCCGG | 8065 |
rs369667949 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108093077 | CGCCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 8065 |
rs369771464 | in-del | -/ATTTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086974 | TTCTCTTTTTATTTT[-/ATTTT]TTTCATTCCTCACCT | 8065 |
rs369821434 | snp | C/T | 0.00101367 | 0.0224901 | intron-variant | CUL5 | GRCh38.p7 | 11:108054854 | TATTCTTAAAATGAT[C/T]GCTATTTTGCTTCTG | 8065 |
rs369833521 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033205 | GACACATTTCTCTCC[C/T]GGCATCAATGTATGA | 8065 |
rs369837207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108056523 | TGAAATAGTTTTGAT[A/G]TTGGCAAAAGGAAGG | 8065 |
rs369850980 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098136 | ACCCATATATCTTCA[A/G]TTAGCTAGTCACTTT | 8065 |
rs369861313 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108075471 | AGTATAAGGGATGTG[A/G]GAAGGTTTGACAGCA | 8065 |
rs369875270 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108044770 | TTTAATTTATTATTA[G/T]TATTTTTTTGAGACA | 8065 |
rs369887422 | snp | C/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106828 | AAAGAAAATCCAGCC[C/T]CCCCCTCCAAAAAAA | 8065 |
rs369891584 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083985 | TTATGAGATTTTTTG[A/G]CGATTTTTTTTCTTT | 8065 |
rs369929530 | snp | G/T | 0.0001327 | 0.00814447 | intron-variant | CUL5 | GRCh38.p7 | 11:108088694 | TTCAACTTTTAAAAT[G/T]ACCTTACTTTGAATT | 8065 |
rs369947709 | snp | A/G/T | 0.000635237 | 0.0178117 | intron-variant | CUL5 | GRCh38.p7 | 11:108009412 | TTTTACTGTGTGGCC[A/G/T]CCGGGTTCGGCTCTT | 8065 |
rs369997430 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108023841 | TTTCTTTTATAAAAG[G/T]AACCTAAAAGTTTAA | 8065 |
rs370041481 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023520 | GTATCCTGGGTGTCT[A/G]GTTGAAGTTGTTGTT | 8065 |
rs370053463 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068041 | TTAAGCAATTCTCCT[A/G]CCTCAGCCTCCCGAG | 8065 |
rs370194703 | snp | C/G | 2.53155e-05 | 0.00355768 | intron-variant | CUL5 | GRCh38.p7 | 11:108089668 | TCTAATACATTACAT[C/G]ATTTATATGTGTGCT | 8065 |
rs370237923 | snp | C/T | 1.6492e-05 | 0.00287154 | missense | CUL5 | GRCh38.p7 | 11:108072410 | ACTTGGAGGAACATA[C/T]CATTAGTGCTGGCCT | 8065 |
rs370252839 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093734 | ATTTTTTCAAGCAAC[A/G]GGATCTTCTGTTGCC | 8065 |
rs370259465 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053559 | ATGCAGAGTTTTGAA[A/G]TAGTCGTCTTATAAT | 8065 |
rs370283266 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108043112 | GGGCATTACTCTGTC[A/G/T]CTCAGGCTGGAGTGC | 8065 |
rs370299473 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042275 | TCCAGGCTGCAGCGC[A/G]GTGGTGCAGTCTCGG | 8065 |
rs370300296 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093585 | TTGATTATTCTTTTT[-/T]GTAAGTAGTCATGTG | 8065 |
rs370323067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031157 | TGGATCATATGAATC[C/T]AGGAGTTCGAGACCA | 8065 |
rs370330619 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108062664 | GATACAGGCATGCAA[C/T]GCATGATAATCACAT | 8065 |
rs370373171 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108019748 | CTAATAATAATAAGT[C/G]ACTGTGTTACTGGTT | 8065 |
rs370425496 | snp | A/G | 0.000153988 | 0.00877327 | missense, intron-variant | CUL5 | GRCh38.p7 | 11:108104196 | TTCTTTTAGGAAGCT[A/G]TCATACAAATAATGA | 8065 |
rs370441097 | in-del | -/GA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018693 | AAAAAAAGAGAGAGA[-/GA]AACATCACATATATG | 8065 |
rs370517276 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079819 | GTTTTGCCTAATCTA[C/G]GACTTTGTATAAATA | 8065 |
rs370522034 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108053865 | TTTCTTTTTTTTTCT[C/T]TTTTTGAGACAGAGT | 8065 |
rs370566362 | snp | A/G | 0.000197876 | 0.00994479 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033891 | ATCTGTTACAAAACA[A/G]CAGTGGTTTGATCTG | 8065 |
rs370585232 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063445 | TTCATTATCCATTCA[A/T]TTGTTGGTGGACAGT | 8065 |
rs370615007 | in-del | -/A | 0.0146672 | 0.084371 | intron-variant | CUL5 | GRCh38.p7 | 11:108011596 | AGAAGCCAATGTCAT[-/A]AAAAAAAACCACCAG | 8065 |
rs370664874 | in-del | -/CTGA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038890 | GTTAAGGTACATTGA[-/CTGA]GATTTTCCCCCCTTT | 8065 |
rs370688876 | snp | A/C | 1.67351e-05 | 0.00289263 | intron-variant | CUL5 | GRCh38.p7 | 11:108097610 | CTGTTTATAGATGCT[A/C]ATTGTTTTCTCCTTA | 8065 |
rs370724594 | snp | A/G | 4.11921e-05 | 0.0045381 | missense | CUL5 | GRCh38.p7 | 11:108094505 | AAAAATAATAAATTG[A/G]CATTACCAGGTATTA | 8065 |
rs370893235 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020597 | ACGTTGCCCAGGCTG[A/G]TCTCAAACTCCTGAG | 8065 |
rs370896820 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108103883 | TTACATGGGTATACA[A/C]GTGTCATGGTCATTT | 8065 |
rs370898882 | snp | A/C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080291 | ATGAGGTCTTGCTGC[A/C/G]TTGCTCAGGCTGGTG | 8065 |
rs370900898 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108058358 | GGTTCATGTGATTCT[C/T]ATGCCTCAGCCTCCC | 8065 |
rs370917519 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099283 | GTGCTGGGATTACAG[A/C/G]TGTGAGCTACCATGC | 8065 |
rs370931311 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108037098 | GGAACTTTTGGGCCT[C/T]TTCCCACCTGGAGGC | 8065 |
rs370963366 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108049623 | GCTGGGACTACTGTA[A/T]GAGCCACCACGCCTG | 8065 |
rs370972008 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | CUL5 | GRCh38.p7 | 11:108072311 | ATGAAATGATTACAT[G/T]AATGTGTTCTCTCCT | 8065 |
rs370976806 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108091380 | GTTAAAAAAAAAATA[A/T]CAAGACCCAACAGTA | 8065 |
rs371047244 | in-del | -/AC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077610 | ACTGCAGCCTGGGCA[-/AC]ACGAGTGAAACTCTG | 8065 |
rs371049503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108046107 | TAGAAACAAATGTGT[A/G]TGTGAGGCAATTACA | 8065 |
rs371051952 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108073201 | TCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGG | 8065 |
rs371086874 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047176 | TAAAAAATTACCCAA[A/G]CATGATGGTGCACAC | 8065 |
rs371101004 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087275 | TAAGAGTTGATGCAT[C/T]CAGTAAAATTTTACA | 8065 |
rs371153063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108065112 | CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACA | 8065 |
rs371314587 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037298 | GCTCAGCTGCTGTTT[C/G]ATACTGTGAATGATT | 8065 |
rs371335791 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016005 | TGGCTCACTGCAGTC[A/T]TGATCTCCCAGGATC | 8065 |
rs371413301 | in-del | -/TC | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032582 | CTAACACATATGGGG[-/TC]TCTCTCTCTCTCTCT | 8065 |
rs371453494 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058209 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8065 |
rs371459190 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098573 | TTTAAAAAAACTTTA[-/G]TTTTTTTTTTTTTTT | 8065 |
rs371484686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033269 | CACCCAACCTTTACT[A/G]TTGAGTTTTGATGGA | 8065 |
rs371487712 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108021517 | AGAGACAGGGTCTTA[A/C]TCTGTCACTCAGACT | 8065 |
rs371627451 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018099 | GACTTTGTCTCTGGA[A/T]GTGCAGAGAGGAATG | 8065 |
rs371664432 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038224 | GGTGTTTTGTTGTTA[A/T]TGTTGTTTTTGCCAG | 8065 |
rs371804055 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108054618 | ATTTTGATCATAATT[A/G]GAGTAATACTTTATT | 8065 |
rs371820038 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108031493 | TAAGAAAGGGGTCTG[G/T]TTTTACTTTTCTGCA | 8065 |
rs371840825 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108074790 | CAGCCTGGGCAACAA[C/G]AGCGAAACTCTGTCT | 8065 |
rs371869929 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108044113 | TATTTGTGTGCTTAT[A/T]GCATCCTAGGCACTG | 8065 |
rs371910503 | snp | C/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108044407 | GTGGTCCCAGCTAGT[C/T]GGGAGGCTGAGGCAG | 8065 |
rs371911612 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108073197 | ACAGATCGAGACTCC[G/T]TCTCAAAAAAAAAAA | 8065 |
rs372017936 | in-del | -/CTCT | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032599 | TCTCTCTCTCTCTCT[-/CTCT]GTTTTTGGCAATGTA | 8065 |
rs372039722 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014406 | AGTGAAAGGGAAGTC[A/G]GGTCAGATTACAAAG | 8065 |
rs372072305 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059985 | GGCATGATAGCTTTT[A/G]CTGTTAGGCACTGGT | 8065 |
rs372123019 | in-del | -/GT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035048 | CTGAGGTGTGTGTGT[-/GT]ACCAGGAGGGGTGAC | 8065 |
rs372126030 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017706 | AATTTAATAATTATC[A/C]AGGCATGTTAGTGCA | 8065 |
rs372154989 | snp | C/T | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105776 | TTTTCTTGCAAATTA[C/T]TTTATATCTTATTTG | 8065 |
rs372161791 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108095907 | TCGAGACCAGCCTAG[-/C]CAACATAGTGAAACC | 8065 |
rs372227025 | snp | G/T | 1.65897e-05 | 0.00288003 | intron-variant | CUL5 | GRCh38.p7 | 11:108098398 | ACTTGATGCAATTCT[G/T]TTTGTAGAAAAAATG | 8065 |
rs372257173 | snp | C/T | 0.000350865 | 0.0132404 | intron-variant | CUL5 | GRCh38.p7 | 11:108073349 | TTTTTTGTGTTATTC[C/T]TTTTCTTTTAAAAAC | 8065 |
rs372279778 | snp | A/G | 0.000413959 | 0.0143808 | synonymous-codon, intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108049916 | CCATCAAGATGATAC[A/G]GCTTTGCTAAAAGCA | 8065 |
rs372301056 | snp | A/C/G | 0.000232352 | 0.0107761 | missense, synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054762 | ACCCTCGTATTTACA[A/C/G]CAAAATGGTGTACAG | 8065 |
rs372320205 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108049034 | CTCTCTTAAAGGATA[C/T]GATTCAGTGGGTTGT | 8065 |
rs372343360 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108054397 | TTTCTTGATTATTCA[G/T]TTAGAAGTCAGTTTC | 8065 |
rs372343538 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018601 | AATCACTTGAACCCA[C/T]GAGGCAGAGGTTGCA | 8065 |
rs372362128 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108095816 | CAAGAAAAATAGAGG[A/C]CGGGCACAGTGGATC | 8065 |
rs372484238 | snp | A/G | 8.57449e-05 | 0.00654714 | intron-variant | CUL5 | GRCh38.p7 | 11:108054621 | TTGATCATAATTGGA[A/G]TAATACTTTATTTTC | 8065 |
rs372523778 | snp | A/G/T | 0.00105081 | 0.022898 | intron-variant | CUL5 | GRCh38.p7 | 11:108104152 | ACTTAAAATAATTTC[A/G/T]TATATTAATGCGCTT | 8065 |
rs372544224 | snp | A/G | 6.81745e-05 | 0.00583803 | intron-variant | CUL5 | GRCh38.p7 | 11:108094808 | CTGATATTCTTCTCT[A/G]TAGCTGATTCAGTTA | 8065 |
rs372570037 | in-del | -/A | 0.285519 | 0.247464 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106836 | CCAGCCTCCCCCTCC[-/A]AAAAAAAAAAAAAAA | 8065 |
rs372585771 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079731 | AGTTACTTCATGTCT[A/G]TTCCCAGTCGGTCCC | 8065 |
rs372594166 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079059 | CATGAGTAGATAGAT[A/C]TTCTTCTCTTTCACC | 8065 |
rs372687738 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108021166 | ACATGCTGTTATTTT[-/T]CACACAACGATGAAA | 8065 |
rs372713518 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065316 | GCATGAGCCACTGCA[C/T]CTGTTGGGAGAAATT | 8065 |
rs372737832 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069666 | TCTCTTCGAGAGCAG[A/G]AATTATATCTTATTC | 8065 |
rs372740707 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant, frameshift-variant | CUL5 | GRCh38.p7 | 11:108073843 | GCTTCCTTGATGTCC[-/T]GCCTCCCTCCACAGC | 8065 |
rs372763965 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090108 | TGTTCTTAATACTTT[C/T]AGTAAAGTATCTTTG | 8065 |
rs372790326 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099744 | CCAGGCAGGCTCTCC[A/G]CCTACCCCAGCTGAT | 8065 |
rs372811412 | snp | A/G | 0.000157987 | 0.00888643 | intron-variant | CUL5 | GRCh38.p7 | 11:108073512 | GGTATATATTCCTAT[A/G]TATATAAAAAACACT | 8065 |
rs372878522 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108084512 | CAGTGGCTAACCCTG[G/T]AGATGGACTGATTCC | 8065 |
rs372886219 | snp | A/C | 3.42883e-05 | 0.0041404 | intron-variant | CUL5 | GRCh38.p7 | 11:108072514 | CAAGGCTATTTTTTA[A/C]ATGTAGGATTATTGA | 8065 |
rs372963669 | snp | G/T | 1.65811e-05 | 0.00287929 | missense | CUL5 | GRCh38.p7 | 11:108089546 | ATGAGGTATCATAAA[G/T]CTCATTTGACACGAC | 8065 |
rs372981378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108101067 | GCGGGTGTAGTCGTA[C/T]GATAAGATGTGCAGA | 8065 |
rs373002565 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077630 | GTGAAACTCTGTCTC[A/C]AAAAAAAAAAAAAGA | 8065 |
rs373042636 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041833 | CTAACCTCAGGTGAT[C/T]CACCTGCCTCGGCCT | 8065 |
rs373059769 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009758 | CAAAGGAAAAACCAA[G/T]AAAATGCTGCCTAAC | 8065 |
rs373067331 | snp | A/G | 0.000313312 | 0.0125123 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033849 | GGATTTTATGCGCCC[A/G]ATTGTTTTGAAGCTT | 8065 |
rs373152682 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026403 | AACATTTCCTCCCCG[A/G]TCTTCTCAGACATTG | 8065 |
rs373173958 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069313 | TTCTTCCTTCCCTAC[C/G]TATGAAATAAAACCC | 8065 |
rs373293131 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033368 | TGTGACCCCAAACCC[A/G]TATCTCAAGTTGTAT | 8065 |
rs373296459 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057303 | AGAGTGCTAGGATTA[C/T]AGGCACGAGCCACGG | 8065 |
rs373303345 | snp | A/G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108108216 | ACCAGCCTGGCAAAC[A/G/T]TGGTGAAACCCTGTC | 8065 |
rs373370751 | snp | A/G | 6.62109e-05 | 0.00575335 | synonymous-codon, intron-variant | CUL5 | GRCh38.p7 | 11:108104333 | GCTAATAGAGCACAA[A/G]TACATCAGAAGAGAT | 8065 |
rs373400120 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035442 | ATCTTTTAAATATTC[A/G]GTAATCTTTGACGGC | 8065 |
rs373410387 | snp | C/T | 3.39271e-05 | 0.00411854 | intron-variant | CUL5 | GRCh38.p7 | 11:108009402 | CCAGCTTGGGTTTTA[C/T]TGTGTGGCCGCCGGG | 8065 |
rs373475957 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060560 | GAAGAATCTGGCTGG[A/T]TGCCGTGGCCCACGC | 8065 |
rs373486473 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039306 | ATTACAGGCATGAGC[C/T]ACTGTGCCCGGCCTG | 8065 |
rs373501220 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092475 | AGTGAGCTAATGAAT[A/C]AAATGTGATTTATCC | 8065 |
rs373525643 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080039 | CTTTAGTCATTTGGG[A/T]TGTATGTAGTAGTAT | 8065 |
rs373547119 | snp | C/T | 0.000105097 | 0.00724828 | intron-variant | CUL5 | GRCh38.p7 | 11:108072287 | TTCTCTAAACTCTTA[C/T]TCTAGTAAATGAAAT | 8065 |
rs373600664 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020693 | GGCCTTGTGTTTGTG[C/T]TTCACGATAAGTGTT | 8065 |
rs373613847 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066784 | TTTGTCCTTAAGTTT[A/G]TAGTATAGTAATGAT | 8065 |
rs373657608 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108049964 | AAAGTTCTTTACACA[A/G]TGTGATATTTTACCA | 8065 |
rs373676569 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082034 | GGAAATGCATTGAAT[G/T]GTATTAATGTTATGT | 8065 |
rs373682792 | in-del | -/TTCTC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016232 | AGAGAGGTTTTTCTT[-/TTCTC]TTCTCTTCTCTTCTC | 8065 |
rs373697712 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071307 | GCTGTGTTGCCCAAC[C/T]TGGAATTCGATGGCA | 8065 |
rs373710434 | snp | A/G | 1.67767e-05 | 0.00289622 | intron-variant | CUL5 | GRCh38.p7 | 11:108072484 | TTTTTTTCAATGGCA[A/G]TGATAGATATATATC | 8065 |
rs373721101 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093903 | GATGGGGGTGTCACT[C/G]TGTTGCCCAGGCTGG | 8065 |
rs373759630 | snp | A/G | 3.33907e-05 | 0.00408586 | intron-variant | CUL5 | GRCh38.p7 | 11:108098376 | AAAGTGTTTTTCACC[A/G]TAAAATACTTGATGC | 8065 |
rs373780539 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085027 | TTCAAAACAAACAAA[A/T]GAAGGTCAACAGAGT | 8065 |
rs373852026 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020288 | ATTCCAGAAGAAGGC[A/G]TTGTTACCATAGGAG | 8065 |
rs373900479 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108034627 | AGGGAACCCTGAGAG[-/AT]TTCCTTTAGGAAAAG | 8065 |
rs373912642 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047042 | GAGGTCTGGGACAGG[A/G]CACAGTAGCTCAGGC | 8065 |
rs373931964 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108088807 | CAGTGCAAGACCTCT[C/T]GGGGGGTTATTTTTC | 8065 |
rs374021793 | snp | C/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032783 | CTGGAGTTTCCATTT[C/G]TTACGCTTTTCTCAG | 8065 |
rs374033647 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011648 | TTTTTTTTTGGAGGG[A/G]GACGGAGTCTCGCTC | 8065 |
rs374068028 | in-del | -/AGAGA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018684 | TGTCTTAAAAAAAAA[-/AGAGA]GAGAGAAACATCACA | 8065 |
rs374074755 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089703 | TAATACATTTTGGAG[A/G]TATTGTTAATGTCAA | 8065 |
rs374199263 | snp | C/T | 1.7079e-05 | 0.00292219 | intron-variant | CUL5 | GRCh38.p7 | 11:108072323 | CATGAATGTGTTCTC[C/T]CCTTCCAGAATTACA | 8065 |
rs374203744 | snp | C/T | 0.000689696 | 0.0185573 | intron-variant | CUL5 | GRCh38.p7 | 11:108097598 | TAGTATTCCATACTG[C/T]TTATAGATGCTAATT | 8065 |
rs374287424 | snp | A/G | 1.6513e-05 | 0.00287336 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108046282 | CAGGGATGTGCATGC[A/G]GTCTGTCTTTGGGAT | 8065 |
rs374338696 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108062697 | GGGCAAATGGTATCA[A/G]TCACCTCAGGCATTT | 8065 |
rs374462322 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031168 | AATCCAGGAGTTCGA[A/G]ACCAGCCTGGGCAAC | 8065 |
rs374495578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059151 | CTGAGTTGCTGGGAC[A/G]GTAGGCGCATGCAAC | 8065 |
rs374506419 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108021624 | GGAGTAGCTGTTGGG[A/G]CTACTGGTGTGCACC | 8065 |
rs374608240 | in-del | -/A | 0.492679 | 0.0600586 | intron-variant | CUL5 | GRCh38.p7 | 11:108096329 | TGCAATCCCATCTCT[-/A]AAAAAAAAAAAAAAA | 8065 |
rs374624388 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060694 | TACAAAAAATTACCC[A/G]GGCATGGTGGTGCGT | 8065 |
rs374633380 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108103366 | GGGGTTCAAGACCAA[C/G]CTGGACAACATAGCA | 8065 |
rs374671303 | in-del | -/TGAG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072536 | GATTATTGAAAATAG[-/TGAG]CGGTTACCAGAGGCT | 8065 |
rs374678528 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048762 | ACCTCCGCCTCCTGG[-/A]TTCAAGCGATTCTCC | 8065 |
rs374803853 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011652 | TTTTTGGAGGGGGAC[A/G]GAGTCTCGCTCTGTT | 8065 |
rs374863024 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018471 | CAGGAGTTCAAGACC[A/G]TCCTGGCCAACATGG | 8065 |
rs374874890 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083177 | TCCTTGTCTTATTCC[C/T]GATTTTAGGGTGCTC | 8065 |
rs374877910 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043640 | ATAAACTTAACTGTA[A/T]AATCTTGGATTGTTT | 8065 |
rs374884994 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038677 | CAAAACTCCATCTCA[A/G]AAAAAAAAAAAAAAA | 8065 |
rs374973043 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089750 | TTATAAGAATATAGC[A/G]TCAGTTAGGCCGGGC | 8065 |
rs374990051 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066632 | CATCAGTTTCTTCCT[A/G]TTTGAATTCCCGTGG | 8065 |
rs374995779 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108065372 | TGTTATTGCTTGCCT[A/G]GAAGTTACAGTCCTT | 8065 |
rs375053670 | snp | A/G | 5.0402e-05 | 0.0050198 | missense, intron-variant | CUL5 | GRCh38.p7 | 11:108104372 | TATCAACACTTTCAT[A/G]TATATGGCATAATTT | 8065 |
rs375060240 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034276 | GCAATGATTGACAGC[A/G]TGTGATATGTTGTCT | 8065 |
rs375060802 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031357 | GCAACAGAACGAGAC[-/T]CTGTCTCAAAAAAAA | 8065 |
rs375152537 | snp | C/T | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008416 | AATTATATTATCTCA[C/T]TGGCCAGTGGTGTGT | 8065 |
rs375154264 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014763 | CCTGCCCTTGTATAA[G/T]TTACATTTTTGTTGG | 8065 |
rs375160465 | snp | A/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032447 | CAGGGGATCAAGGCT[A/T]CAGTTAGCTATGATC | 8065 |
rs375169346 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099426 | ACCAATTGCATTTCT[A/G]TGGGGCAATAAATAA | 8065 |
rs375171004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108079365 | CCCACCTCAGCCTCC[C/T]AAAGTGCTGGGATTA | 8065 |
rs375173353 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050736 | TTATTAGGTTACCTT[C/T]TGATATCTTTATGTT | 8065 |
rs375207902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108095369 | AGCTGGGAGATGAGC[A/G]TGTATTCTGGGCAGT | 8065 |
rs375224151 | snp | C/T | 3.89393e-05 | 0.00441227 | intron-variant | CUL5 | GRCh38.p7 | 11:108078143 | GTATATTTTCAATAT[C/T]AAAAATATTTTATTC | 8065 |
rs375233014 | in-del | -/TT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083850 | TAGGTGGTGTGGCTA[-/TT]TTGGAGGTGTGGAGG | 8065 |
rs375281503 | in-del | -/TTTTTTTTTTTTTTTTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048649 | ATAGACTCCACCACC[-/TTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 8065 |
rs375302722 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108078444 | TTTATTTTTTCAGGT[-/A]AAAAAAAAATATTCC | 8065 |
rs375350556 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101665 | GGAACTGAGGGAGAG[G/T]CAGAAGTGCAGATTA | 8065 |
rs375351387 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014294 | CTGCAGTGTAAGCAG[A/G]GCTGCATGCTGTGTT | 8065 |
rs375400747 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087533 | CAGTGGCATGCACCT[A/G]TAGTCCCAGCTACTC | 8065 |
rs375406207 | snp | A/C | 1.65583e-05 | 0.00287731 | intron-variant | CUL5 | GRCh38.p7 | 11:108097631 | TTTCTCCTTATTCTT[A/C]ATAGTCTTTAGTAGC | 8065 |
rs375474858 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013347 | ATTTTTATCTCTTAG[C/T]TCTGATCTGAGCTCT | 8065 |
rs375479574 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075572 | AGGGAAGTTCGCTGT[A/G]TCGCCCAGTCTGGAG | 8065 |
rs375495536 | snp | A/T | 1.70927e-05 | 0.00292336 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009310 | GCCGGGAGCGCCACG[A/T]ATTCTCGCGTCGTCT | 8065 |
rs375538241 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098591 | TTTTTTTTTTTTTTT[A/T]AAATTTTGAAATCTT | 8065 |
rs375541820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108083921 | GCATGCGGCCCAGGA[C/T]GGCTTTGAACGTGGC | 8065 |
rs375547513 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | CUL5 | GRCh38.p7 | 11:108074747 | GGAGGTGGAGGTTGT[G/T]GTGAGCTGAGATCGT | 8065 |
rs375577788 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093933 | GTCTTAAAATCCTGG[C/T]TTCAAGTGATCCTCC | 8065 |
rs375619760 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CUL5 | GRCh38.p7 | 11:108058442 | TTTAGTAGAGACAGG[G/T]TTTCACCGTGTTAGC | 8065 |
rs375677162 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084579 | GATAACATCATCTTG[A/T]TCTTGTGTGATTCTT | 8065 |
rs375715187 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076234 | AGATGAGTTCTCAGT[A/G]TGTTGCCCAGGCTGT | 8065 |
rs375723444 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057343 | GTAACGGTCAAAAGT[G/T]TGAAATGAAATAGGA | 8065 |
rs375729688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108099128 | TCCCACCTCTGCCTC[C/T]GGATTAGCTGGGACC | 8065 |
rs375781794 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028026 | CCTCAGGCTTGGGTC[A/T]CCATCTTTATGTATC | 8065 |
rs375810718 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023797 | GGTTTCAAAAAATAC[A/G]AGTATTGCTAGAATT | 8065 |
rs375857435 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065561 | TTCATCCTACTTTTG[A/C]TTTCTGCTGTGAAAG | 8065 |
rs375903062 | snp | C/T | 6.6335e-05 | 0.00575874 | intron-variant | CUL5 | GRCh38.p7 | 11:108098400 | TTGATGCAATTCTTT[C/T]TGTAGAAAAAATGCA | 8065 |
rs375979743 | snp | C/G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099982 | TACAGGCACATGCCA[C/G/T]GGCACCTGGCAGCTA | 8065 |
rs376032882 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108055908 | AGTGTTGGGATTACA[C/G]GCGTGAGCCACTGCA | 8065 |
rs376046804 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047881 | CTGGAAATAAACTTA[C/T]GAAGAATTACCTTGG | 8065 |
rs376194733 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CUL5 | GRCh38.p7 | 11:108095001 | TTGTAAGTAGATAGT[A/G]TGTTAGTTATTTCAG | 8065 |
rs376213696 | in-del | -/TTTG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030040 | TATGGTTCTTTCATA[-/TTTG]TTTATTTGCACACCT | 8065 |
rs376225345 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037386 | GTCCAACTTCTAACA[C/T]CAGCTGTGTTGGCAA | 8065 |
rs376250841 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101068 | CGGGTGTAGTCGTAC[A/G]ATAAGATGTGCAGAG | 8065 |
rs376254020 | snp | C/T | 0.000330196 | 0.0128448 | intron-variant | CUL5 | GRCh38.p7 | 11:108104151 | TACTTAAAATAATTT[C/T]GTATATTAATGCGCT | 8065 |
rs376265419 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080640 | ACCTCGTGATTTGCC[C/T]GCCTCGGCATCCCAA | 8065 |
rs376271612 | snp | A/G | 8.72989e-05 | 0.0066062 | intron-variant | CUL5 | GRCh38.p7 | 11:108072298 | CTTACTCTAGTAAAT[A/G]AAATGATTACATGAA | 8065 |
rs376279213 | snp | A/G | 0.000134932 | 0.00821267 | intron-variant | CUL5 | GRCh38.p7 | 11:108050075 | TCGAAAGGTAAGACT[A/G]TTTTTCTCCTTGTTT | 8065 |
rs376308780 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108079653 | TTAAGTGTACATTTG[-/A]AGTCAGATTTGACAA | 8065 |
rs376383717 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070706 | TAAAAAAAAAAATTG[G/T]ACATATACCTACTAC | 8065 |
rs376394703 | in-del | -/GTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038229 | TTTGTTGTTAATGTT[-/GTT]TTTGCCAGTCTGTGT | 8065 |
rs376477951 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024296 | TGATCATGCCTGTAA[A/T]CCTAGCAGTTTGGGA | 8065 |
rs376496161 | in-del | -/CA/CACACACACA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108091695 | CCTGTCTCTCTCACT[-/CA/CACACACACA]CACACACACACACAC | 8065 |
rs376509999 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033170 | TGCGAGCTTATCTTG[C/T]CCTCTCCCCATGTGG | 8065 |
rs376557504 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108031804 | ACTGGATAAAGAAAA[C/T]GTGGTACATATACAC | 8065 |
rs376593480 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037898 | CACACGGGTCTGTCT[G/T]AGGATAGCAGTCTCA | 8065 |
rs376595361 | in-del | -/CTC | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108016133 | ATTGCCCAGACTGGT[-/CTC]CACTCCTGAGCTCCA | 8065 |
rs376609259 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061430 | GATTTTTTAATATAT[A/G]GAAATCTATACCATA | 8065 |
rs376620084 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102691 | CTGAATAGTGCCTGA[C/G]TCCCAAGTCTGTTGA | 8065 |
rs376639125 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031062 | AATATCAACAGATTT[-/T]GTATAACTGAAAAAT | 8065 |
rs376724227 | snp | A/T | 0.000168896 | 0.00918801 | intron-variant | CUL5 | GRCh38.p7 | 11:108033950 | TGCTAGCATAAAGGA[A/T]ATTTTAGTGATGTCT | 8065 |
rs376761076 | in-del | -/CAGG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017755 | CATGGGAGGCTGAGG[-/CAGG]AGGATTGCTTGAGCA | 8065 |
rs376870985 | snp | A/C/T | 3.96686e-05 | 0.00445343 | intron-variant | CUL5 | GRCh38.p7 | 11:108098565 | GTCTGAAGTTTAAAA[A/C/T]AACTTTAGTTTTTTT | 8065 |
rs376922169 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050933 | TTTCAGCTCTTCAAA[C/T]TCCGTCCTCATTTTC | 8065 |
rs376929978 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026857 | GGCTGGGCATGGTGG[C/T]GGGCACCTGTATTCC | 8065 |
rs376944548 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108023133 | CTGTAATCCCAGCTA[A/C]CTGGGAGGCTGAGGC | 8065 |
rs376955289 | in-del | -/TG | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108069394 | TTCTCTTCCACTGTC[-/TG]TTTCTTCTCTACCAT | 8065 |
rs377005519 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033509 | ACATACTTTTTAGAC[A/G]TAACTTTCTAAGTGT | 8065 |
rs377022965 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007757 | TTTTGTTTGTAGTTT[C/T]TTTTTGTTTTTTTTG | 8065 |
rs377035348 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108049556 | CTATGTTGCCCAGGT[A/T]GGTCTCAAATTCCTG | 8065 |
rs377050615 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108021393 | TCAGCTTGTCTTTTC[A/G]TCTTAGCTTTTCTTA | 8065 |
rs377099233 | in-del | -/TTAG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089755 | AGAATATAGCGTCAG[-/TTAG]GCCGGGCGCACTGGC | 8065 |
rs377116209 | snp | C/G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103089 | ACATGAGCCACCACA[C/G/T]CCGGCATATACATGC | 8065 |
rs377138159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108058318 | CAGTAGTGCAGTCTC[C/T]GCTCACTGCAACCTC | 8065 |
rs377221831 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016328 | CTGGAGTACAGTGGC[A/G]CAGTCACAGCTCCCT | 8065 |
rs377313847 | snp | A/G | 6.72755e-05 | 0.00579942 | intron-variant | CUL5 | GRCh38.p7 | 11:108088504 | ATCATTTTTCCATCA[A/G]CTGCTTTTAATTTGT | 8065 |
rs377372641 | snp | A/C/G | 9.89012e-05 | 0.00703149 | missense | CUL5 | GRCh38.p7 | 11:108070144 | TCATTTAAAGAGACT[A/C/G]TCTTAGCTGAGTGCC | 8065 |
rs377376049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108083962 | CATTTGTAAACTTCC[A/G]TAAAACATTATGAGA | 8065 |
rs377421711 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015479 | ATTAAGAACTTGTCA[A/G]TTTTTCATTGGGTTG | 8065 |
rs377423629 | snp | A/G | 0.000255496 | 0.0112997 | intron-variant | CUL5 | GRCh38.p7 | 11:108104164 | TTCGTATATTAATGC[A/G]CTTTTATTTTTATTT | 8065 |
rs377430759 | snp | C/G | 4.94645e-05 | 0.00497291 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033874 | AAGCTTTTACGCCAG[C/G]AATCTGTTACAAAAC | 8065 |
rs377464273 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093706 | TTACATTTTTTAAAA[A/G]TTTATTTATTTAATT | 8065 |
rs377521625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108066205 | CAAACTTAGCCAGGC[A/G]TGGTGGTGGATGCCT | 8065 |
rs377541000 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108062090 | ACAGAGCCAAAGCAT[A/G]TCACAATCTATATTA | 8065 |
rs377562924 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108046768 | TGTAATTTATTTAGA[C/T]TGTCCTTTGTATTGC | 8065 |
rs377583037 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070632 | CTAAAGGATTTTTTT[A/T]TTACTTCAATGTTTT | 8065 |
rs377600609 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015762 | AACAATTACCATAAT[C/G]TGGAGGTGATGTATG | 8065 |
rs377639810 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077727 | AGGCAGGCAGATCAC[C/T]TGAGGTGAGGAGTTT | 8065 |
rs377651586 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098904 | ATAATAAGTAACACC[C/T]ACACATGATTGTTTT | 8065 |
rs377700822 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069549 | TCTAAGTTTTTTTTT[-/T]ATTTTGTGTGTGTTT | 8065 |
rs377753698 | snp | A/C | 1.93015e-05 | 0.0031065 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033778 | ATTTAAATTAAACTC[A/C]CTTTTATCTTTTTTT | 8065 |
rs386362614 | in-del | -/A | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106852 | AAAAAAAAAAAAAAA[-/A]TTTAATTTTTAAAAA | 8065 |
rs386374829 | in-del | -/A | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106837 | CAGCCTCCCCCTCCA[-/A]AAAAAAAAAAAAAAA | 8065 |
rs386757298 | multinucleotide-polymorphism | CT/TC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043156 | TAGCTCATTGTAACC[CT/TC]GAACTTCTGAGTTCA | 8065 |
rs386757299 | multinucleotide-polymorphism | CGA/TGT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059940 | GAATTAAATGAAATA[CGA/TGT]TACATTAAGCATTTG | 8065 |
rs397721156 | in-del | -/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108042237 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 8065 |
rs397722921 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038693 | AAAAAAAAAAAAAAA[-/A]GATCTTTCATCTCCT | 8065 |
rs397746807 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016806 | ACAAACAAAAAAAAA[-/A]CAAACAAAAAGCAGG | 8065 |
rs397781042 | in-del | -/A | 0.375 | 0.216506 | intron-variant | CUL5 | GRCh38.p7 | 11:108044520 | CTCAAAAAAAAAAAA[-/A]TTAGAATATAAAACA | 8065 |
rs397799618 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070631 | CTAAAGGATTTTTTT[-/T]ATTACTTCAATGTTT | 8065 |
rs397959679 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077643 | CCAAAAAAAAAAAAA[-/A]GAAAAAAAATCTCAC | 8065 |
rs398017497 | in-del | -/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108031380 | CTATGAAACTCATGA[-/T]TTTTTTTTTTTTTTT | 8065 |
rs398017498 | in-del | -/A | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108049251 | CAAATATTGTGAAAG[-/A]AAACTAGTCACAAAA | 8065 |
rs398017499 | in-del | -/A | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108062222 | GGATGTTAAAAAGAT[-/A]AGAGGTATTTAAGGA | 8065 |
rs398017500 | in-del | -/A | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108098591 | AAGATTTCAAAATTT[-/A]AAAAAAAAAAAAAAA | 8065 |
rs398045552 | in-del | -/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108080127 | TTTTTTTTTTTTTTT[-/T]CCGGTATTCGTATAT | 8065 |
rs398045553 | in-del | -/A | 0.5 | 0 | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108108025 | AATAAAAAAAAAAAA[-/A]TTCCAACCTGAAAGT | 8065 |
rs398115803 | in-del | -/TAAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063660 | TAATAAAATTTAAAA[-/TAAA]AAAATAAATAAATAG | 8065 |
rs527294330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033158 | GAGAGTTCCAAATGC[A/G]AGCTTATCTTGCCCT | 8065 |
rs527308490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108026302 | AAATCCATGACCACA[A/G]TGAGGCCAGTCATAC | 8065 |
rs527332479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108067911 | ATTTTATATGTGTAG[G/T]CTTTTCTTTATTTTT | 8065 |
rs527347643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108060672 | AAAGCCCTGTTTCTA[C/T]TAAAAATACAAAAAA | 8065 |
rs527365642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108020344 | TCCCGAAGACTTTCC[A/G]GTGGGACAAGATGTG | 8065 |
rs527371374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100563 | AAAGCAAACAAAAAC[A/C]AACAAAAAACCTTAC | 8065 |
rs527438346 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047345 | AAACAAAAAGGTCTG[A/G]TCTGATGGCTAGAAG | 8065 |
rs527493203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108061197 | ATGGCTTATCACTAT[A/G]CTTTCCATTCAAGAT | 8065 |
rs527571860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108088009 | GAAAGTGAAATGGAG[A/T]TACAAATTCTTTATT | 8065 |
rs527586948 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007915 | GGATTACAGGTGCCC[A/G]CCACCATGCCCGGCT | 8065 |
rs527601791 | snp | A/G | 5.1106e-05 | 0.00505474 | intron-variant | CUL5 | GRCh38.p7 | 11:108095029 | CAGCTTTCAGTTTGG[A/G]TGAAAGTAGCAGGAC | 8065 |
rs527637858 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106800 | AGCAGGGATATAACC[C/T]GCAGTTAAGTGAAAA | 8065 |
rs527651175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011733 | CCCGGGTTCAAGCGA[G/T]TCTTCTGCCTCAGCG | 8065 |
rs527662028 | snp | A/G | 6.7539e-05 | 0.00581076 | intron-variant | CUL5 | GRCh38.p7 | 11:108052650 | TTACAATTTGTTCTT[A/G]TTTTCCTAGCTTATG | 8065 |
rs527695121 | in-del | -/ATAA | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108051908 | TACATAAGAAAGCAG[-/ATAA]ATAAGTAACAGCTGG | 8065 |
rs527723759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059539 | TTACCAGCTGTCTGC[A/G]TTTTGGCAAGTTATT | 8065 |
rs527760699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108093266 | GTCACACCCCCTGTA[A/G]TTTGGATGATCTTCT | 8065 |
rs527788266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012285 | TCCAGTTTATTGTTC[C/T]ACCCCAAACAGCAAT | 8065 |
rs527795642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099802 | GTTCTAGGTTTTCAT[A/G]TAAATGGAACCAGAC | 8065 |
rs527799407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108092851 | AGACAGAGTCTCACT[C/T]TGTTGCCCAGGCTGG | 8065 |
rs527805884 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033064 | AGTGAAAGCTGTTGT[A/G]CCCATAGTTATGATT | 8065 |
rs527833266 | in-del | -/AAG | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108011002 | GACTCTAAATGAAAA[-/AAG]AAAAGGAAAGAAAAT | 8065 |
rs527869228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039687 | TGAATTTGCTTATCT[A/G]GATAACTCATATAAA | 8065 |
rs527891837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108046125 | TGAGGCAATTACAAG[C/T]GTACTTGGTTTATAT | 8065 |
rs527921712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108086322 | ACAATATAAGACTAA[C/T]AGCTAGCTTGTAATC | 8065 |
rs527955028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108072727 | ACAAAGAAATTATAA[A/G]TGTTTGAAGTGATGG | 8065 |
rs527964818 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026100 | CTCCGCCTTACCCAA[C/T]ATAAATTCTCTTCTC | 8065 |
rs527965570 | snp | G/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107055 | TGATGGTCACAATGA[G/T]ATAAATATTAGAATA | 8065 |
rs528012847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108040141 | CTCCTAGATTTTTCT[A/G]ATAAAGTTTTTAAAA | 8065 |
rs528015818 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053091 | ATAAAAGGTAACTAG[C/T]TCATTAAAAGGTTAG | 8065 |
rs528015847 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108043310 | AACTTCTGGCCTCAA[A/G]TGATCCTCCTGCCTT | 8065 |
rs528037380 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083432 | CAGAAGTGAGGATTG[A/C]TGGGTTTCTCTTAGT | 8065 |
rs528116684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108091604 | TGAGGTGGGAGGATC[A/G]CCTGAGCCTGTGAGG | 8065 |
rs528125000 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108025698 | TTTCCCCAGTCTCTT[-/A]ACAGTTTTCTCACAC | 8065 |
rs528128333 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108084644 | CTAGTCCTATGAAGA[A/C]AGATAAATTAATGAC | 8065 |
rs528140725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108077840 | ATCCCAGCTACCCAG[A/G]AGGCCAGCTAAGACA | 8065 |
rs528176362 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108085282 | GCTATATGCTACAAG[A/G]TAGATGAACCTTGAA | 8065 |
rs528200054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038094 | CCTTTGGGAAATTAA[A/G]GTTTAGTAAGAAACA | 8065 |
rs528233084 | snp | A/G | | | intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108061096 | ATCTCAGGCAAACAT[A/G]CAGGAGTTGATGGCA | 8065 |
rs528247024 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108024580 | CAGTGATTCAGTGAT[A/T]TACACATCTACGCTG | 8065 |
rs528293244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031193 | GGCAACATGGCGAAA[A/C]CCCGTCTCTACTGAA | 8065 |
rs528318295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108078487 | ATCTCTACTTGTTTT[C/T]CCCTCATTAGTCACT | 8065 |
rs528350365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108065723 | TTCCTACCCTCTTCA[A/G]TGCCTCTTGCAGTGA | 8065 |
rs528366962 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108106181 | AGAAATAATTTTGTA[A/G]TAATTGTGGCCCTTA | 8065 |
rs528372385 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018015 | CCTGGGCTTTTCTTA[A/T]AAGTCTGGTTATTCC | 8065 |
rs528381629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108071606 | AGGCTGAGTGCAATG[A/G]TGCAATCACGGCTCA | 8065 |
rs528381876 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060113 | GTTATAAATTATTAA[A/C]ATTAAAATAAGCACT | 8065 |
rs528494128 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108036638 | ACCCACCACTGTGCC[A/G]GGCTAATTTTTGTAT | 8065 |
rs528542807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023795 | TGGGTTTCAAAAAAT[A/G]CAAGTATTGCTAGAA | 8065 |
rs528543381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108076239 | AGTTCTCAGTATGTT[G/T]CCCAGGCTGTTCTTG | 8065 |
rs528590027 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108103419 | GAGAAGAAGGGGAAA[A/T]AAAAAACCTTAAAAA | 8065 |
rs528597918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069557 | TTTTTTTTATTTTGT[A/G]TGTGTTTGTGTATGT | 8065 |
rs528648170 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037253 | TTTTCAAATTTCATA[G/T]GTAATTTTTACCTGT | 8065 |
rs528648286 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063918 | GCCTGTCTTATAGAT[A/G]AAAGCTACTTTAACT | 8065 |
rs528649744 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108009871 | CCTCCCACTCCACCC[C/G]CCTTCCTCCCTTTTC | 8065 |
rs528696301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108010814 | TCAGAAAGAAAATTT[A/G]TGGGCTGGGCACAGT | 8065 |
rs528700771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108057790 | TTAAATTGATAGTAT[C/T]GTACCAATACTATTT | 8065 |
rs528708393 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038759 | TAGGTAAAGGGATTT[C/G]TGACTGACAATAATT | 8065 |
rs528714858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064287 | TTGAAATGAACATAC[A/G]GATTTTGTCTGCCAT | 8065 |
rs528725554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108051342 | GTATCAATTCTGGGG[C/T]CACAGTTTTTGGATT | 8065 |
rs528810552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108097567 | GCCTATGTTGATTAT[C/G]TGGGAGAATTGATCT | 8065 |
rs528811292 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108043348 | AAGAGTGCTAGGATT[-/AC]AGACATGAGCCAATA | 8065 |
rs528819496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108038794 | CCCTTGTAAATTTTA[A/G]CCATATTTTGGCCAT | 8065 |
rs528838510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031250 | GTGCGTGTCTAATCT[C/T]AGCTACTCGGAGGCT | 8065 |
rs528870888 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108046132 | ATTACAAGCGTACTT[A/G]GTTTATATGAGTGAA | 8065 |
rs528874794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018745 | CACATTTATTTTTAT[C/T]AAGCCACCTCACTTT | 8065 |
rs528874870 | in-del | -/TC | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032581 | CTAACACATATGGGG[-/TC]TCTCTCTCTCTCTCT | 8065 |
rs528880224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108045118 | GTACTAGTATTAAAT[A/G]TATTTCTATAATGAA | 8065 |
rs528880593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038274 | TTATTGAGAATAGTG[C/T]TTGTTCTCTGAGTAC | 8065 |
rs528924271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108077957 | TCATCTCAAAAAAAC[A/G]AAACCAAACCAACAA | 8065 |
rs528939088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085680 | TTGATGCTAAGTAAA[A/G]GAAGTGGGTCACAAA | 8065 |
rs528947879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071685 | CCAAGTATCTGGGAC[C/T]AAAGACATGCACCAC | 8065 |
rs528985716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108078628 | TTCTATAATTGGTAA[A/G]ATGAATATGCCTGTG | 8065 |
rs529025398 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108031649 | TCCATTGGTCTTTGT[A/G]TATGTTCTTATATCA | 8065 |
rs529034153 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028494 | AACCCTTGCCCCTTA[C/T]AATATATTCTCAACA | 8065 |
rs529038020 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108059606 | GGAATAGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 8065 |
rs529039480 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CUL5 | GRCh38.p7 | 11:108073048 | CTACTAAAAATACAA[A/C]AAAAATAGCCAGGCG | 8065 |
rs529046360 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108066490 | TATTCATACAACTCA[C/G]TCTGTTACTTTTTTT | 8065 |
rs529049295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108093787 | ATCAGAGCTTAAACT[C/T]CTGGGCTCAAGCAAT | 8065 |
rs529055621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108026046 | CTGTCATGATGGGAA[A/G]CAGAAGTCTCTTTCT | 8065 |
rs529082309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108065970 | TTCTTATTCCTGACC[A/G]TTTGTATTTATTCTT | 8065 |
rs529090170 | in-del | -/TTTTTTTTTTTTTTTTTTTTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048664 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTTTTT]GAGGTGGATTCTCAC | 8065 |
rs529116014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108072525 | TTTAAATGTAGGATT[A/G]TTGAAAATAGTGAGC | 8065 |
rs529123979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059923 | ACCCTTTTGTATTAG[C/G]AGAATTAAATGAAAT | 8065 |
rs529212325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011784 | AGGCGCACGCCACCA[C/T]GCCCAGCTAATTTTT | 8065 |
rs529234299 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102585 | ATCCACCCACCTCAA[C/T]CTCCCAAATTGCTGG | 8065 |
rs529286636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030530 | TAATCCCAGTTACTC[A/G]GGAAGCTGAGGCAGG | 8065 |
rs529294508 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108064426 | AAATTTGGTTTGCTA[G/T]TCTGGGCTCAGTGGC | 8065 |
rs529294597 | in-del | -/AAAT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108074833 | AAATAAAAATAAAAC[-/AAAT]AAGTAGGTAAAGTAG | 8065 |
rs529360284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108058373 | CATGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 8065 |
rs529390091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016569 | TTTCTCTTAATAAAT[A/G]TTTTGCTTAGTGTCC | 8065 |
rs529414232 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035197 | CTGTAAGAAGTGGGC[A/G]AAGGGGCTACACTCT | 8065 |
rs529415713 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104527 | CTTACAAAAACAACT[A/G]TATTTTGCCAATCAC | 8065 |
rs529419511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108098223 | TTAACAGGTTAGTTA[C/T]CATGTTTAAGGAAAA | 8065 |
rs529462664 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108051909 | ACATAAGAAAGCAGA[G/T]AAATAAGTAACAGCT | 8065 |
rs529463172 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CUL5 | GRCh38.p7 | 11:108090005 | AGATCGTGCCATTGC[A/C]CTCCAGCCTGGGTAA | 8065 |
rs529500261 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108051494 | GATTAAATGAGTTAC[A/T]TGCAGACAATACATA | 8065 |
rs529529275 | in-del | -/T | 0.0535932 | 0.154675 | intron-variant | CUL5 | GRCh38.p7 | 11:108044740 | TGGTAATTTTTTTAC[-/T]TTTTTTTTTTATATT | 8065 |
rs529593641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096374 | CTTGGTGGCTGTATC[C/T]CCAGCTACTTGGAAG | 8065 |
rs529659505 | snp | C/G | 0.00341605 | 0.0411868 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009308 | TGGCCGGGAGCGCCA[C/G]GAATTCTCGCGTCGT | 8065 |
rs529716454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108090330 | AGTCTCTATTAAAAA[C/T]ACAAAAAAATTAACG | 8065 |
rs529753519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108089650 | TTTTTAAATATTTGG[C/T]TTTCTAATACATTAC | 8065 |
rs529863366 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107179 | TTTTTTATTTAAGTC[A/T]CTTGCTCTTATTTTG | 8065 |
rs529912330 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024718 | CTTTTGTACAACAGA[C/T]ACCACATTACAAAAT | 8065 |
rs529921826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023272 | ACAAACAAAAAAAAC[C/G]CAGTATCTTCTCCAC | 8065 |
rs529937299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042982 | TGGCCAGGTTGGTTG[C/T]GAACTCCTGGCCTCA | 8065 |
rs529942777 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108083900 | GCTTGTCCAACCCTG[C/T]GGGCTGCATGCGGCC | 8065 |
rs529976832 | in-del | -/GTTTTTTTT | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007772 | TTTTTTGTTTTTTTT[-/GTTTTTTTT]TTGAGACAAGAGTCT | 8065 |
rs530031783 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034281 | GATTGACAGCGTGTG[A/T]TATGTTGTCTACCAG | 8065 |
rs530034735 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033336 | AGGGATTTCAGTCTC[C/T]GTGTTGAGTGACCCC | 8065 |
rs530036252 | in-del | -/A | 0.0209421 | 0.100162 | intron-variant | CUL5 | GRCh38.p7 | 11:108044352 | AGACCGTGTCTCTAC[-/A]AAAAAATAAAAAATT | 8065 |
rs530038573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108048574 | TTTCACTGTTACATC[A/G]GTGGCATTCTGTTGG | 8065 |
rs530044016 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108037271 | AATTTTTACCTGTCA[A/C]AACAGACAGAAGCTC | 8065 |
rs530046288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108035996 | AGTCCGAGTGATCAG[C/T]GAGACTGTCCTAAGT | 8065 |
rs530050962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108029966 | AATTGAAATTAGAAA[A/G]TATCCTCTTGTTAAG | 8065 |
rs530060597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024186 | CTTGGATTTGATTTC[A/C]TGCCCTGCCACTTAC | 8065 |
rs530077661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108081609 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 8065 |
rs530098372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108074971 | CATGGGAAGGAGTTA[C/G]TTTTTACTGTGAGTA | 8065 |
rs530106522 | snp | A/C/G/T | 6.83718e-05 | 0.00584653 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009314 | GGAGCGCCACGAATT[A/C/G/T]TCGCGTCGTCTCGCG | 8065 |
rs530188603 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108028915 | TAGAAACCAAAGTCT[G/T]TATAATGGCCTTCAG | 8065 |
rs530196217 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080604 | TTTCACCATGTTGAC[C/T]AGGATGGTCTCAATC | 8065 |
rs530213328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108081935 | TTCAAGATCATTCTG[G/T]CTATTTGGGTTCCCT | 8065 |
rs530221679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108062187 | ATAGTTTATTTCTTA[G/T]AAATAGTGCTTTCTG | 8065 |
rs530240415 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108035072 | GGGTGACAGGAAAGA[A/G]AGAACTAGAGTCAGG | 8065 |
rs530256535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108075554 | CTCTAGAAGTGACTT[G/T]TCAGGGAAGTTCGCT | 8065 |
rs530272073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021376 | TATTTCTTGCTCTTC[C/T]TTCAGCTTGTCTTTT | 8065 |
rs530334068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028552 | AATAAGATTATGACA[C/T]TTCAGGCCAGGTGCG | 8065 |
rs530368647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108009791 | GTTTCAGTGACTCGA[C/T]CCCCCACTTCTTCCA | 8065 |
rs530370012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108062931 | GCTCACCGCAACCTC[C/T]GCCTCCTGGGTTCAA | 8065 |
rs530385877 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090153 | CTACTGTTTCACTCC[C/G]ATTTGTACCTCAACT | 8065 |
rs530386977 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108097442 | AGAGAGCATTTATTG[C/G]TTTCTCATAACCAAC | 8065 |
rs530387394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090373 | GGGGGGCCTGTAGTC[C/G]CAGCTACTTGGGAGG | 8065 |
rs530396107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015377 | TGGATGTGATACGAA[A/G]ATTTGAATATCATCG | 8065 |
rs530410785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102654 | TATCTATATAGGGGA[A/G]GTTGAAGGAGTTTTT | 8065 |
rs530414592 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035753 | CAAGACCTTGTCTCA[-/A]AAAAAAAAAAAAAAT | 8065 |
rs530459649 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058078 | GCCGGACGTGGTGGC[A/G]TGCACCTGTAATCCC | 8065 |
rs530460542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108014750 | TAGGCAGACAGCTCC[C/T]GCCCTTGTATAATTT | 8065 |
rs530523131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043035 | CCCAAAATGCTAGGA[C/T]TAAAGGCATGAGCCG | 8065 |
rs530536341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050528 | CGTGCTACCACACCC[A/G]GCTATTTTATTGTAT | 8065 |
rs530552767 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108064004 | ACATCTTCCTTTCCA[A/G]TTTGGATGCTCTTTC | 8065 |
rs530553463 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043560 | TTCTTGTTTAATAGA[A/T]TGGAGGGTTTCAAGA | 8065 |
rs530554486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010111 | GGCAGATTCTCCACC[A/G]GTTAAAAAGTTTGGA | 8065 |
rs530557390 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066343 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAACCAGA | 8065 |
rs530663081 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059527 | ACAGATGTTATTTTA[C/T]CAGCTGTCTGCGTTT | 8065 |
rs530685417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071097 | ATTGAAAAATTATTT[A/T]TGAATACAGTTTTAT | 8065 |
rs530702603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024539 | CCTAACATGTAACAG[C/T]CAGATATTATAAAGT | 8065 |
rs530723397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108077774 | ACATGGTGAAACTCC[A/G]TCTCTACTAAAAATA | 8065 |
rs530747025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037541 | TGTGTGTGGCAAAGT[C/T]CAGGAGAAACGAAAT | 8065 |
rs530771806 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017315 | GGCTTGCTTGAGCCC[A/G]GGAGGTTGAGGCTGC | 8065 |
rs530841497 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100275 | AGGCTCGGCGCGGTG[A/G]CTCACACCTGTAATC | 8065 |
rs530843472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108070393 | AATTTTAAGCATTTT[C/T]CCTCTTAGCTATCAA | 8065 |
rs530853874 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108097275 | CCTGCCTCAGCTTCC[C/T]AAAGTGCTGGAATTA | 8065 |
rs530856354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108075104 | GGAAGAAAGAATACC[A/G]GTTAAGAACTTATTT | 8065 |
rs530856519 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028665 | GACATGGTGAAACCC[C/T]GTCTCTACTAAAATA | 8065 |
rs530875798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031083 | ACTGAAAAATAATCA[G/T]GAGTCTGGGCCTGGT | 8065 |
rs530876184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108076081 | TCACCCAGGCTGGAG[A/T]GAGTGCAGTGGCACA | 8065 |
rs530882717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023924 | TTGGAAAACAGTGTC[C/T]TCTTCCTCCTCCTCC | 8065 |
rs530895049 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108029698 | AGTTTAATAGAAAAC[A/T]ATTAATTATTAAATT | 8065 |
rs530982285 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108023084 | TGAAACCCCACCTCT[A/C]CTAAAAAAAATAGCC | 8065 |
rs531002494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108063805 | TAGTTTTTTGAGGAA[A/C]CTCCAAACTGCTCCA | 8065 |
rs531010331 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041202 | TACACCCAGCTTTCT[C/G]TAGCCCATTTTCCTT | 8065 |
rs531021225 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108022469 | GGATTGTTACAGATA[C/G/T]GCTAATTGCTTGAAA | 8065 |
rs531041317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108063003 | GGCATGCACCACCAC[A/G]CCCGGCTAATTTTGT | 8065 |
rs531042656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069462 | TTTTAGGGCTTGTAC[G/T]TACTTTACAGGATCC | 8065 |
rs531082908 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108029053 | ATGTTTCTATCTTAT[C/G]TTCTTTGCATTGGCT | 8065 |
rs531123039 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013987 | TGGAGAATGCAAAGA[C/T]ATGTAGAACAATGTC | 8065 |
rs531136205 | in-del | -/TGCA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016397 | TCATCCTCCCACAGG[-/TGCA]TGCAACACCAGCATT | 8065 |
rs531201258 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108021243 | TCTAATCCACAATCA[G/T]TATGGCGGGAACTTC | 8065 |
rs531226977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108009796 | AGTGACTCGACCCCC[C/G]ACTTCTTCCATTTCT | 8065 |
rs531235877 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108096971 | TTGTACTCATTAGCC[C/G]CCTGCTCACAACTAC | 8065 |
rs531278262 | snp | C/G | 1.66023e-05 | 0.00288113 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054750 | TAGAACACAAGCACC[C/G]TCGTATTTACAACAA | 8065 |
rs531300380 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108014461 | TTGAAATAAAGTTCT[A/C/G]TAGTTACTGAGGAAT | 8065 |
rs531305290 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108020432 | GTGTGTCTTAGTTTT[A/T]AATGAAAAAGATTGA | 8065 |
rs531305715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108095179 | TACTTAAGATACTGC[C/T]GTTGTCTACAGAATT | 8065 |
rs531315859 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108021249 | CCACAATCAGTATGG[C/T]GGGAACTTCACAAAT | 8065 |
rs531317477 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086070 | AAAGTGTCTAAAACC[A/G]TATATAATTGGAGTC | 8065 |
rs531325094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108061285 | AAATGGGAAGAAATA[C/T]AAAAGAGGAATAACA | 8065 |
rs531413640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108048156 | CATTTTACTTAGGCA[A/G]TCTTCAGTTGAACAT | 8065 |
rs531434974 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008590 | ACTGGCCTCAAGTGA[C/T]CCTCCCCCTTCGGCC | 8065 |
rs531436660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108101681 | CAGAAGTGCAGATTA[G/T]TTCCCTCATACTGTG | 8065 |
rs531494145 | snp | A/G | 8.44901e-05 | 0.00649907 | intron-variant | CUL5 | GRCh38.p7 | 11:108095722 | TTTGTTTTTAAGACT[A/G]TATCCTCTCATGTAG | 8065 |
rs531531134 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108041811 | TGGCCAGGCTGGTCT[C/T]GAACTCCTAACCTCA | 8065 |
rs531540334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108049380 | AGGGTATTGCTCTGT[C/T]GCCCAGGCCAGAGTG | 8065 |
rs531541743 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108055529 | CAATTATACCTCACT[C/G]TAACTCCTGGGCATA | 8065 |
rs531544413 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108046430 | ATAATATCATATTTT[A/G]TTATTTTGAAAGTAG | 8065 |
rs531544589 | in-del | -/ATT | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108055454 | GAGGTAAAAATATTA[-/ATT]ATTATTATTTTTAGA | 8065 |
rs531553008 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043632 | GCTCCACCATAAACT[G/T]AACTGTATAATCTTG | 8065 |
rs531555776 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077850 | CCCAGGAGGCCAGCT[A/G]AGACAGGAGAATCAC | 8065 |
rs531621065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108089295 | ACTAACAATTTGGTT[A/G]TAGTCTCAGTTTTGC | 8065 |
rs531628007 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052965 | TAATTCTGCTTAAAA[G/T]AATGTATAAAAATTC | 8065 |
rs531729187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108053938 | GCAACCTCCACTTCC[C/G]AAGTTCAAGCAATTT | 8065 |
rs531734915 | in-del | -/GGGTGG | 0.0170352 | 0.090705 | intron-variant | CUL5 | GRCh38.p7 | 11:108019205 | GATGGGTGGGGGTGG[-/GGGTGG]GGGTGGGGTGGGGTG | 8065 |
rs531748718 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027971 | TCTCCTTTGCTAGTT[C/G]TTACTCCTCTCTCCG | 8065 |
rs531867901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108047028 | CCTTTCTATAACATG[A/G]GGTCTGGGACAGGGC | 8065 |
rs531874237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039719 | GGAATCGTATAGTAT[C/T]TGTCGTTTGGAAAGA | 8065 |
rs531895346 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069938 | TTGGTAAACTAGTAT[A/T]GCATATCCATCTTCA | 8065 |
rs531902626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033231 | TATGACAGTATGCAC[A/G]AGTACCATCAAATAG | 8065 |
rs531905839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050822 | ATAAATTCAGTATAT[A/G]CTGTGCTTATTTTCT | 8065 |
rs531936641 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108101951 | ATCAGGAGCCTGGTA[C/T]CTGAATACCATCAAG | 8065 |
rs531955707 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108027245 | AGGCCTTAGTAGCTG[G/T]GATTATAGGCGCCAC | 8065 |
rs531999318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074160 | CCATTCTCCAGTAGG[A/C]TTTTTTTCTCACTCT | 8065 |
rs532008140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108062810 | CTGTTATGTTATCAA[A/G]TACTATGTTTTATTC | 8065 |
rs532037107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108081251 | CGAGATCGTGCCATT[A/G]CACTCCAGCCTGGGT | 8065 |
rs532077219 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009276 | CCTGGTGGGAGCTCC[A/G]GCCTCCGGTCAAGGC | 8065 |
rs532078977 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008754 | TGTAAGCATTTCAGG[A/C]CAATGCACCTCCCTT | 8065 |
rs532096037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108014692 | CATTTATTCATTGAA[C/T]GAGAATTTAGTATTT | 8065 |
rs532112541 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107587 | ATCCTCATATGGTCT[A/G]TACGATTTTGAATGT | 8065 |
rs532119045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015286 | GAGCAAGTCATGTAC[A/G]TATTTAGAAGAGTTC | 8065 |
rs532122708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108055667 | ACAAGGGCTCTCTCT[C/G]TTGCCCAGGCTGGAG | 8065 |
rs532125113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095808 | TGTCTTATCAAGAAA[A/C]ATAGAGGCCGGGCAC | 8065 |
rs532168917 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108062021 | ATCACCTCCCACCAG[C/G]TCCCTGTCTCAACAC | 8065 |
rs532211559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108056429 | TTCAGAAATCACACC[A/G]AGTTGGATGTCTTTT | 8065 |
rs532213387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048848 | ATTTTTGTATTTTTA[C/G]TAGAGATGGGGTTTC | 8065 |
rs532229608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096177 | ATAGGCAAGTTACCA[A/G]GGCAGAGAAAAGTGC | 8065 |
rs532290938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108083782 | TACCCTGTCTCAAAG[C/T]AGAAAATTTCTGTGG | 8065 |
rs532293295 | snp | C/T | 1.6543e-05 | 0.00287597 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108089509 | CTTGGTACTTAAGTA[C/T]GTACAGAACAAAGAT | 8065 |
rs532325118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090221 | GGGCTGGGCACGGTG[G/T]CTCACACCTATAATC | 8065 |
rs532326705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042324 | CCCGGGTTCAAGCAA[C/T]TCTCATGCCTCAGCC | 8065 |
rs532349215 | in-del | -/T | 0.0279526 | 0.114869 | intron-variant | CUL5 | GRCh38.p7 | 11:108057198 | ACTACACCTGGCTAA[-/T]TTTTTTATTTTTTGA | 8065 |
rs532351112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108049455 | CAAGCAATCCTCCCA[A/C]CTCAACCTCCTAAGT | 8065 |
rs532376421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108054525 | TTGTCTTATATAATT[A/G]TATGTTCTCTTGAGC | 8065 |
rs532394667 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108040347 | CTGGGTGTGGTGGCT[C/T]ATGCCGGTAATCCCA | 8065 |
rs532404885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108047132 | ATACCAGCCTGGGAA[A/G]CATGGTGAGACCTTG | 8065 |
rs532415087 | in-del | -/TT | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108019661 | ATTGTGCTGTCACTC[-/TT]ATAAAAGTCTAGCAC | 8065 |
rs532455994 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108081464 | CCATTATCAAAAATC[A/G]GTTGGCTGCCAGGCG | 8065 |
rs532468878 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108035881 | GCCTAGCCTCAGATC[C/G]AGGTAATTGAGATCT | 8065 |
rs532536080 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010214 | GTACGGACAGAAATG[C/G]GGGTAGTGAATAGCT | 8065 |
rs532579149 | in-del | -/TTTTTTTTTTTTTTTTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048668 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTT]GAGGTGGATTCTCAC | 8065 |
rs532658626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087944 | CACTCCAGTCTGGGG[A/G]ACAAGAGCAAAACTC | 8065 |
rs532667396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108040958 | TACCACACCATTCCC[C/T]GTTATCCTATGAGAC | 8065 |
rs532706632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034954 | CCACCCCTTTTGTCC[G/T]GATCATTTATCTAGT | 8065 |
rs532710606 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085815 | TAGAGAATGGGATTT[A/G]ACTGCTGGCAGGTGT | 8065 |
rs532722339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066718 | CTTATCAAGCACCAG[C/T]TGTGTGCCAGGACAC | 8065 |
rs532734268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108020556 | TTTTTTTTGTTTTTT[C/G]TTTAAAATAGAGACA | 8065 |
rs532780375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108031756 | TCACTCTAACAAAGA[C/T]GTGAAATCACCCCCA | 8065 |
rs532813866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108068445 | CACCTCAGCCCCCCA[A/G]CTCGCAGGGACCACA | 8065 |
rs532818497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021293 | AACTGGTTGTGTGGT[G/T]TTCAAAATGTTATGG | 8065 |
rs532858486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108066622 | ATCTAGCCTTCATCA[A/G]TTTCTTCCTATTTGA | 8065 |
rs532873672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018986 | CCTCAGAAAAAAATT[A/G]CGTCTGTATTGAATA | 8065 |
rs532873871 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108093062 | CTCAGGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 8065 |
rs532910972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108026089 | AAGTCCATTTTCTCC[A/G]CCTTACCCAACATAA | 8065 |
rs532918908 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043053 | AAGGCATGAGCCGCC[A/C]TGCCCGGCCTGTTTC | 8065 |
rs532929154 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075187 | TGGTCAAAAGTAGTT[C/T]GATAATTTTTTTTTT | 8065 |
rs532956938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108060559 | AGAAGAATCTGGCTG[A/G]ATGCCGTGGCCCACG | 8065 |
rs532958450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012431 | CTCCTATGTTCTTCT[C/G]TGTTCCATGCTACCT | 8065 |
rs532959544 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041763 | GCCTGGCTAATTTTT[C/T]GTATTTTTAGTGGAG | 8065 |
rs532963990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039643 | TTCTTCATTCTTCCT[C/G]TCCTCAGCTCCATTT | 8065 |
rs532993857 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108059979 | GTGCCTGGCATGATA[A/G]CTTTTACTGTTAGGC | 8065 |
rs533002128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108079494 | CTCCTTATATACATT[C/T]GTCAGTCAACTTTTT | 8065 |
rs533014500 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108073090 | GCCTATAGTCCCAGC[G/T]ACTTGGGAGGGTGAG | 8065 |
rs533024583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108054067 | GCCAGGCTGGTCTTG[A/G]ACTCCTGACCTCAAG | 8065 |
rs533038838 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090800 | CGAGCAAGCACACAC[A/G]AGAGAGACCTACAGA | 8065 |
rs533124359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108019600 | TAACGTAGTAGTGCA[A/G]TAACACATCACTCGT | 8065 |
rs533130641 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107730 | TAAGTTGTATAATTT[A/G]TTTTCTTGCAAAATA | 8065 |
rs533146676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108017250 | AAATAAATACCTGGG[A/G]GTGGTGGTGTACGGT | 8065 |
rs533168414 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106961 | TCCCATCTGGAAAAT[A/G]TTAACTTGTGTTGCC | 8065 |
rs533187065 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108067159 | GTAAGTATCTGCCTC[A/C]TGAGGTTGCCATGTG | 8065 |
rs533246419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100269 | AACTTTAGGCTCGGC[A/G]CGGTGGCTCACACCT | 8065 |
rs533248914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011659 | AGGGGGACGGAGTCT[C/T]GCTCTGTTGCCAGGC | 8065 |
rs533253483 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007256 | GGGTATACTGGCTGA[C/G]TTTTGACAAGTGCAT | 8065 |
rs533262407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099153 | GGGACCACAGGCATG[C/T]GCCACCACACTCAGC | 8065 |
rs533284656 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108106065 | AGGTAGCAAATGTCA[A/G]TTATTAGACCGAGCA | 8065 |
rs533297379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100409 | CTAGCCAGCTGTGGT[A/G]GCGCATGCCTGTAAT | 8065 |
rs533322240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108092669 | ATTCCAGGAGTTGGG[A/G]CCAGGAGGGGAAATG | 8065 |
rs533325683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108098127 | TGAATCCTAACCCAT[A/G]TATCTTCAATTAGCT | 8065 |
rs533344130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108058868 | CTGGGCCTATAGCAG[A/G]TGAACAGAAATGTAT | 8065 |
rs533348402 | in-del | -/CTC | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108050327 | TTTTACTTTCTCCTT[-/CTC]CTGGTATTCAGTATT | 8065 |
rs533350533 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036156 | TAAAATTCCAAAAGT[A/G]TATTTCTTCCATCTG | 8065 |
rs533359711 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018303 | GAATTACTGGTATTC[A/C]AATATATACAATCAG | 8065 |
rs533498956 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108098241 | TGTTTAAGGAAAATA[C/T]ATAGAGTTTGTTTTA | 8065 |
rs533515798 | in-del | -/ATT | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108046534 | ATCGTCATTAGTTGG[-/ATT]ATTTTTTTCCCACAG | 8065 |
rs533536402 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032997 | GTAAGCTTGGGGGAT[C/T]CCCAAAACCACTCTC | 8065 |
rs533571015 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108052589 | TTTGATTTCCTTTTT[G/T]GGTGTTTGTACATGA | 8065 |
rs533642283 | in-del | -/TAAAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108073311 | TTAAATGAGTTTTAT[-/TAAAA]TTATGTTTATTTTCT | 8065 |
rs533691673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085842 | GTGTGGGGTTTCTTT[C/T]TGGGGTAATGAAAGT | 8065 |
rs533714209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108045928 | ATACATCTATTGTGT[C/T]AAAGAATTAAAAGGA | 8065 |
rs533732326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099620 | CACAATGGAATGTAT[C/T]TTTCAAAGTATAATT | 8065 |
rs533737310 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108047302 | GCTTGGGCAGCAGAG[A/T]GAGACCCTGTCTCAA | 8065 |
rs533746202 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107044 | TAGAAAAATTTTGAT[A/G]GTCACAATGAGATAA | 8065 |
rs533747761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108046594 | TATATTTAATTAAAA[G/T]ATGCTATAGCGAATT | 8065 |
rs533770687 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108060131 | TAAAATAAGCACTTA[C/T]TAACCTTCAGTATTT | 8065 |
rs533875631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032644 | TTTTTCCTAATATTG[C/T]ACTACTTTTACATTC | 8065 |
rs533926410 | snp | C/T | 7.92833e-05 | 0.00629566 | intron-variant | CUL5 | GRCh38.p7 | 11:108094526 | CCAGGTATTATTTTA[C/T]AATTACATGTATATA | 8065 |
rs533929502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012565 | TTTTTTCTCCTATGC[C/T]TATAAGAAAGTTCAT | 8065 |
rs534075070 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108080912 | TCTTTTGTTGCTTTT[C/G]CTTTTGGTTTGGTTT | 8065 |
rs534101163 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012858 | TACCTCGGCCACCCA[A/G]AGTGTTGGGATTACA | 8065 |
rs534106089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108087527 | TGGGTGCAGTGGCAT[A/G]CACCTGTAGTCCCAG | 8065 |
rs534161499 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108044752 | TTACTTTTTTTTTTA[A/T]ATTTTAATTTATTAT | 8065 |
rs534175069 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036454 | AAAGTACAAAGTCAT[C/T]TTTCAACCCCCCACT | 8065 |
rs534198766 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051089 | TAGTGTAACCTGGGC[-/A]TTGTTGCCCCATCCC | 8065 |
rs534224320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108052174 | ATGGGTCTTACTGTG[C/T]TGCCGAGGCTGGTCT | 8065 |
rs534261823 | snp | A/G | 0.000340187 | 0.0130375 | intron-variant | CUL5 | GRCh38.p7 | 11:108078130 | TAAAAATTTATCTGT[A/G]TATTTTCAATATTAA | 8065 |
rs534407204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039043 | TTTTTAAATTGAGAT[A/G]GAGTTTCATTCTTGT | 8065 |
rs534413045 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108069847 | TATATTTTTCTCTCC[A/C]CTCCTTGAGGACTTT | 8065 |
rs534433568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071435 | GCCTGGCTAATTTTT[G/T]TATTTTTTGTAGAGG | 8065 |
rs534474026 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102471 | AGCTGGGACCACAGG[C/T]GCGTGCCACCATACC | 8065 |
rs534474393 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104686 | GGAGAAATACAGTTG[A/G]GAAGGGTGAGGGTGG | 8065 |
rs534498806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108071988 | TTGAGACCAGCTTGG[A/G]CAACATTGGGAGACC | 8065 |
rs534505824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108058500 | TGATCTGCCCGCGGC[A/G]GCCTCCCAAAGTGCT | 8065 |
rs534542308 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106510 | TTTGGGGAATGAACA[A/G]CAGCAAATACTGTAA | 8065 |
rs534558591 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056433 | GAAATCACACCGAGT[C/T]GGATGTCTTTTCCCT | 8065 |
rs534563683 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056168 | CCTTAGGGTGCTTCA[A/G]TATAAGGAAAGTTAG | 8065 |
rs534593328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030200 | GACTCTGAATTTCCC[A/G]GTAGCCAACACTAAG | 8065 |
rs534597308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108098324 | AGCATATTTTTAAAT[A/C]TTTTCTCTCAGACAT | 8065 |
rs534602254 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108079441 | AAATGTTCAAACTTA[A/C/T]AATAGAGTTACTATG | 8065 |
rs534628719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108097929 | GATGTTTACTTTTCT[A/G]TATTTTTCATTGATA | 8065 |
rs534652180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010416 | GATATTTGATTGTCT[A/G]ATAGATGGGACTGTC | 8065 |
rs534678348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064073 | TTATTTTGAATAAAA[C/G]TGGTGACAGTGGGCA | 8065 |
rs534748647 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108034107 | CTGAACATACAATCA[C/T]ACTCACAGCTTTGAG | 8065 |
rs534762550 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025659 | GCTGATTGTTCTGCC[C/T]ATTCCCATTCCTTCC | 8065 |
rs534785444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108009470 | GCGAAGTGTGGGAGT[A/G]TTCAGGGGTTGTCCA | 8065 |
rs534806191 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108056012 | TTGAACTCCTGGCCT[A/C]AAGCAATCCTTCTTG | 8065 |
rs534819267 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108063070 | GGCTGGTCTCGAACT[A/C]CTGACCTCAGGCAAT | 8065 |
rs534829934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023968 | AGAAATGTCTTTTAC[A/G]TAGTGATGTTTCCGC | 8065 |
rs534833442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108016273 | CTCTTCTCTTCTCTT[C/T]TCTTTTCTGTTGAGA | 8065 |
rs534838562 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108062010 | TTGCTGATCCAATCA[C/T]CTCCCACCAGGTCCC | 8065 |
rs534866380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050582 | CATGTTGGCCAGGCT[C/T]GTCTCGAACTCCTGA | 8065 |
rs534867939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108058936 | GAGCTGTGCTGCTGA[A/G]CAGGCATGTTGACAG | 8065 |
rs534919880 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081621 | GCCAGGCGTGGTGGC[A/G]GGCACCTGTAGTCCC | 8065 |
rs534969492 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108043075 | GCCTGTTTCTTTTTT[A/T]AAAAAATTGTTTTTA | 8065 |
rs534983388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084032 | TTAGTGTTAGTGTAT[C/T]TTATGTATGGCCCAA | 8065 |
rs534983740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102264 | CGAACTCCTGACTTC[A/G]TAATCCGCTCCCCTT | 8065 |
rs535023661 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090500 | CATCTCAAGAAAAAT[A/C]AAATAAATAAATAGA | 8065 |
rs535038584 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016803 | AAAAACAAACAAAAA[A/C]AAACAAACAAAAAGC | 8065 |
rs535063424 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108026338 | TTCCAGAGTCACTTA[-/T]TCTTCCACTTTCCTA | 8065 |
rs535104397 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108087834 | GCCGGGCATGGTGGC[A/G]GGCACCTGTAATCCC | 8065 |
rs535114764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096621 | GCTCAGGCTGGAGTG[C/T]AATGGCGCAATCTCA | 8065 |
rs535146509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108065186 | GCCCGCCACCACACC[C/T]GGCTAATTTTTTGTA | 8065 |
rs535175729 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108089881 | CGCGTCTCTACTAAA[A/T]ATACAAAAATTAGCT | 8065 |
rs535181443 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108097096 | AATCTCAGCTCACTG[C/G]AACCTCCATCTCCCA | 8065 |
rs535197022 | in-del | -/GT | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108035038 | GACTGACTTACTGAG[-/GT]GTGTGTGTGTACCAG | 8065 |
rs535197043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042564 | TTGATAAAATATCCT[C/G]TCTCCTATTTTTGTA | 8065 |
rs535259727 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064776 | AGGATTTTTGCATCA[A/G]TATTCATCAGTGATA | 8065 |
rs535339608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108083372 | CTACAGAGGATAATA[C/T]TGTACATTGAATATT | 8065 |
rs535406670 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035248 | ACTACAGCTTTTGGT[A/G]GGAACCACCAGTTGG | 8065 |
rs535428223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108016176 | TGCGTAGGCCTCCCA[A/G]AGTGCTGGGATTACA | 8065 |
rs535519416 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108053675 | CTTAAGTGGTATACC[A/G]TGCTTTTTTTTTTTT | 8065 |
rs535542221 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108071327 | ATTCGATGGCACGAT[C/T]ACAATTCACTGTAGC | 8065 |
rs535548544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050687 | CCCTTACTAGAAATT[A/C]AATTACTTTTCTCCC | 8065 |
rs535554844 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108082374 | CAGTGTTGCCCTCCT[A/G]AGCTCGAGTAATCCT | 8065 |
rs535581928 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108024651 | TAAAATTTATTTACA[C/G]ATGTCAGATATTCAA | 8065 |
rs535590033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016943 | TAGATTGGGCAGCAT[A/T]GCAAGACCTACCACC | 8065 |
rs535615033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011329 | TACTTACCTGTGGAA[C/G]CTACTTTGGTTCATA | 8065 |
rs535646742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037054 | ATACAAACTTTTAAC[A/G]TTTTTGGTCCACCCA | 8065 |
rs535652559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043827 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA | 8065 |
rs535734145 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108065012 | AATTTTATTTCATTT[A/T]ATTTATTTAATTAAT | 8065 |
rs535753791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108077135 | CAGATCCAAGGATTG[A/G]CCTAGGGCATTCTGA | 8065 |
rs535783284 | in-del | -/TTATT | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108014897 | CTCTTATTATTATTA[-/TTATT]TTTATTTTTATTTTT | 8065 |
rs535790435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084773 | CACAATGAGCTATCA[C/T]TTCATACCCAGTAGG | 8065 |
rs535821291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096679 | TTAAGCGATTCTCCT[A/G]CCTCAGCCTCCCAAG | 8065 |
rs535854468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108103087 | ACACATGAGCCACCA[C/T]ACCCGGCATATACAT | 8065 |
rs535880483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108063992 | AAGCGTAGTTTGACA[C/T]CTTCCTTTCCAATTT | 8065 |
rs535945997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108083082 | TTCCTTTCCAGTTTG[G/T]TTCTATTTTCTTTTC | 8065 |
rs535949728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108090599 | AAATGATAACAATAA[A/G]TACTTCTGTATAGCA | 8065 |
rs535951609 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076160 | ACCTCAGCCTCCCGA[A/G]TAGCTGGGACTACAG | 8065 |
rs535998899 | in-del | -/TTG | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108039995 | GGGTCACACTATTTC[-/TTG]TTCTCTTCTACACAA | 8065 |
rs536009968 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051641 | CCAATGTTTATATAC[C/T]ATTTTTATCATTTTA | 8065 |
rs536017615 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108029258 | TGTTGGCTTCCCCAC[G/T]GCCCATTTGTGTGAG | 8065 |
rs536020116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108095913 | CCAGCCTAGCCAACA[C/T]AGTGAAACCCCATCT | 8065 |
rs536039676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030290 | GTTCAGGAGAGAAGC[A/G]TAGCTAATCCCAGTA | 8065 |
rs536100478 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108075746 | ATCTAGCTATGTTGT[C/T]TGGGCTGGTCTTGAA | 8065 |
rs536123536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015594 | AGAGATGGTTGCATT[C/T]GACACAGCCTAGGGA | 8065 |
rs536134296 | in-del | -/CTC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068140 | CAGGCTGGTCTTGAA[-/CTC]CTCCTGACCTCAGGT | 8065 |
rs536177604 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108030349 | GTCCTTATGATAAGA[A/G]TACAGTGGCTGGGTG | 8065 |
rs536183661 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087080 | TTTTTTTGTTTTGCA[A/C]ATGGCTCAGGAGGTG | 8065 |
rs536191911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108022654 | AACGCATTTTTAAAA[A/G]TTAAGTTATTCTTCT | 8065 |
rs536253863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108041989 | ACTTTTGTTATAGTA[A/T]ACTAAATAAAAGATG | 8065 |
rs536258412 | in-del | -/TCATA | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108057090 | CAATTTGTATGTTAG[-/TCATA]TCATAGCCACATTAA | 8065 |
rs536264382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108041346 | GCAGTGGCATGATCT[C/T]GGCTCATTGCAACCT | 8065 |
rs536289348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108073585 | TGCATTATTTTTCTA[C/T]TAATTATAAACTTAA | 8065 |
rs536337830 | snp | A/G | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108106080 | ATTATTAGACCGAGC[A/G]TATTGTGAAGAATTA | 8065 |
rs536350749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108067589 | AAAACTGATTTCACA[A/G]CATACAGTCTGAAAC | 8065 |
rs536375741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108027895 | CACACTTTATTTACT[C/T]TTTGTCCAGAATACC | 8065 |
rs536382427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108035301 | AGATACATAAGACCA[A/G]TCAGCAGCTTGATTT | 8065 |
rs536494677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068838 | GCTATCTTACCTGAA[A/G]TAGTTCAACAGCCTC | 8065 |
rs536517349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108063154 | CCGACTATTCATTCT[C/G]GTTTTTTTGTACCCA | 8065 |
rs536518001 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108055805 | CTGGCTAATTTTTTT[A/T]TTTTTAGTAGAGATG | 8065 |
rs536537792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095846 | CACGCCTGTAATCCC[A/G]GCACTTTGGAAGGCC | 8065 |
rs536559481 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101215 | TCCTCATTCATTGCT[A/G]TTTGCATAGGTGGCA | 8065 |
rs536581160 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031351 | GCCTGGGCAACAGAA[C/T]GAGACTCTGTCTCAA | 8065 |
rs536605086 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061615 | TGTTTGTTTTCCTTT[C/T]TTTTCCATTCCTTCC | 8065 |
rs536608052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108027367 | AACTCCGCCTCCCAG[A/G]TTCAAGCAATTCTCC | 8065 |
rs536788992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108019985 | CTCTTTTTAACAACC[A/G]ACTCTCAGGGAACTA | 8065 |
rs536797020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013980 | GGTACCATGGAGAAT[A/G]CAAAGATATGTAGAA | 8065 |
rs536806297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023299 | CCACTCTGTGGGCTG[C/T]CTTTTCACTCCCTGA | 8065 |
rs536814282 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081784 | GCTATGATGTATGTG[C/T]TTATTTTTGAATGCT | 8065 |
rs536837281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108054841 | GCAATTCCCTTGATA[G/T]TCTTAAAATGATTGC | 8065 |
rs536895137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069762 | ATGTATTCACACTTC[C/T]AGAATTTTATAACCT | 8065 |
rs536909764 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093208 | CTTTTGCCTTCTTGT[A/G]TAACTTGACAGAGTA | 8065 |
rs536927087 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CUL5 | GRCh38.p7 | 11:108077413 | CACTTTGAGAGGCTG[A/C]GACAGGTGGATCACT | 8065 |
rs536934658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108009925 | ATTCTCCCATTCTTG[A/G]GTTCATCTTTTTCCT | 8065 |
rs536992586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108103892 | TATACACGTGTCATG[A/G]TCATTTGCTGCACCC | 8065 |
rs536995921 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108016226 | GTCAGCCAGAGAGGT[C/T]TTTCTTTTCTCTTCT | 8065 |
rs536996841 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008095 | CCCGGCCTCTTTGCA[A/G]TATTTATCACAACTC | 8065 |
rs537040942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108036001 | GAGTGATCAGCGAGA[C/T]TGTCCTAAGTCCTTT | 8065 |
rs537046069 | in-del | -/AAAT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063657 | AATTAATAAAATTTA[-/AAAT]AAAAAAATAAATAAA | 8065 |
rs537067806 | snp | A/G | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108006813 | GTATTTTTAGTAGAG[A/G]CAAGGTTTCACCATG | 8065 |
rs537097499 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108020487 | AAAAGTTTATAGAAT[-/A]AGGATATAAAGAAAG | 8065 |
rs537155583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108061648 | TCTATTTCCCTCCCC[A/G]TTTTGCCTCCCTTCC | 8065 |
rs537155924 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108068698 | TTTAGTCCTCACAAC[C/G]TATTAATTTCATCTG | 8065 |
rs537169013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108075879 | CTGATGTTGTCTCAG[C/T]CCTGTCATCTCACTG | 8065 |
rs537177632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108029371 | TCTGAAGAGCCAGTG[A/C]ATGAGAGAATTGTAG | 8065 |
rs537194974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108101391 | TGTTGGTAACTGCTG[C/T]TGTTGTCTACAGCAG | 8065 |
rs537218416 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059849 | AGATCACACCATTGC[A/G]CTCCAGCCTGGGTGA | 8065 |
rs537264994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030151 | CCAGGCATAAAGTTA[C/T]TGTACAAAGTATATG | 8065 |
rs537274532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108022882 | TAAAATTGAGTTGTT[C/T]TGCTTTTCTTATGGA | 8065 |
rs537288858 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108063270 | AATTGTTTTAATTTT[C/T]AGCTTCCACAAATGA | 8065 |
rs537311655 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047282 | TGATCATGCCATTGC[A/G]CTCAGCTTGGGCAGC | 8065 |
rs537314234 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108049708 | TTTTTATCTATTTTG[A/T]ATAATGCTGCTGTGA | 8065 |
rs537342199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108089706 | TACATTTTGGAGATA[C/T]TGTTAATGTCAAAGA | 8065 |
rs537348204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108082483 | TCTCTCACTGTGTTG[A/T]CCAGGCTGGTCTTGA | 8065 |
rs537365234 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011392 | CATCCACAGCACAGA[C/G]CTGTGAATGGGAAAA | 8065 |
rs537376372 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108096500 | AAAAATTTTTTTTTT[A/T]AAAAAAGAGAAAGAT | 8065 |
rs537415445 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108020889 | CTCACTACTCACTCA[A/C]TGACTCACCTAGAGC | 8065 |
rs537416830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108093926 | CAGGCTGGTCTTAAA[A/G]TCCTGGCTTCAAGTG | 8065 |
rs537420267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013077 | ATAAAAGTATTAGCA[A/G]CCTCCTGATTATCAA | 8065 |
rs537498124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068161 | GACCTCAGGTGATCC[A/G]CCCGCCTTAGCCTCC | 8065 |
rs537537036 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108065523 | GGTCTAAATGCTCCC[C/T]CCATGGGCATGTGTC | 8065 |
rs537551014 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108027177 | CTCACTGTCGCTGTC[A/G]CCTAGGCTGGAGTGC | 8065 |
rs537552414 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007536 | GAATGGAGAACTTAT[A/T]GAAGTCAGAGTTGTA | 8065 |
rs537554355 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099375 | TATAGATCATGTAAT[A/C]GGATAATGTGGCAGA | 8065 |
rs537590609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108014091 | TCAGATGTGTTACCA[A/G]CTGCTCTATGCTCCC | 8065 |
rs537601453 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042273 | TGTCCAGGCTGCAGC[A/G]CAGTGGTGCAGTCTC | 8065 |
rs537614699 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009018 | AGGCTAATCCGAAGG[A/G]GTCGGGGAGGCTCGT | 8065 |
rs537622412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095923 | CAACATAGTGAAACC[A/C]CATCTCTACTAAAAA | 8065 |
rs537632615 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108048934 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG | 8065 |
rs537639279 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100779 | CTCACGCCTGTAATC[C/G]CAACACTTTGGGAGG | 8065 |
rs537642513 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075575 | GAAGTTCGCTGTGTC[A/G]CCCAGTCTGGAGTGC | 8065 |
rs537658328 | in-del | -/AA | 0.0271762 | 0.113356 | intron-variant | CUL5 | GRCh38.p7 | 11:108048251 | CATTTTTTAAAGAAC[-/AA]AAAAAAAAAAGTAAA | 8065 |
rs537661216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108102239 | TTCACCATGTTGGCC[A/G]GGCTGATCTCGAACT | 8065 |
rs537672766 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017033 | TCAAAGGTAATTGAT[C/G]TGTGTAGCTGTGGTT | 8065 |
rs537717034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042053 | CCACATTAGAGAGAC[A/G]TTTGCATGATAAATA | 8065 |
rs537769441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108073747 | TTCCAAGAATGTTTT[C/T]CTGTTTTTGAATATT | 8065 |
rs537781867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034335 | CTCAGGATTTTTATG[G/T]GGGCTGGTCACATAG | 8065 |
rs537785983 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019148 | AGCAAATGCTATGCC[A/G]TTTTCTATCAAGGAC | 8065 |
rs537787364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108027460 | TATTTTCAGTAGAGA[C/T]AGGGTTTCACCATGT | 8065 |
rs537810312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108022642 | ACACAGGACCCAAAC[A/G]CATTTTTAAAAATTA | 8065 |
rs537934869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108072206 | ACAACAACAAAAAAA[C/T]GAACAACTACTCCTA | 8065 |
rs537941722 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108015512 | AGAAATTGCCCTCTT[A/G]AAACGTATATCTAAG | 8065 |
rs537975292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108079294 | TATTTTTAATGGAGA[C/T]GGGGTTTCGCCATAT | 8065 |
rs537982551 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108094592 | TAAATTAAAAATAAA[A/C]CTCAGCAGTAATAGA | 8065 |
rs537991349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108031912 | TCCTTAGCAAACTAA[C/T]GCAGGAACAGAAAAC | 8065 |
rs537996233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108081090 | TCAGGAGTTCAAGAC[C/T]AGCCTGGCCAAGATG | 8065 |
rs538012708 | in-del | -/TTTATTTTTTAAG | 0.0023933 | 0.0345097 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107705 | GCTTAATTTTTGGAT[-/TTTATTTTTTAAG]TTTATTTTTTAAGTT | 8065 |
rs538079071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108025799 | GCCACAAATTCTAGT[C/T]ACCTCAGCCTTTTCA | 8065 |
rs538132184 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108072938 | CTGGGCAAGGTGGCT[C/G]ACGCCTGTAATCCCA | 8065 |
rs538134119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012593 | CATATGTCGCGTCAT[A/G]TAAACTTTTCTTTTT | 8065 |
rs538196647 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050791 | TATAATTTCCCTTTT[A/G]CTTAACTCTTCTATT | 8065 |
rs538238301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108039205 | TTTTGTATTTAGTAG[A/G]GATGGGGTTTCTTCA | 8065 |
rs538245858 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108045437 | TCTCTACCAAAAATT[A/T]AAAAAACTAGACAGG | 8065 |
rs538250493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108038537 | AAAATTACCTGAGTG[C/T]GGTGGTGGGCCTCAG | 8065 |
rs538439313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108027987 | TTACTCCTCTCTCCG[C/G]CTCTTAATGTTGGAT | 8065 |
rs538448512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108035294 | CCATATCAGATACAT[A/G]AGACCAATCAGCAGC | 8065 |
rs538465355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032464 | AGTTAGCTATGATCA[C/G]TCCACTGCCCTCCAG | 8065 |
rs538477739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108072799 | GCATTGAAATATAAC[A/G]TTGTACCCCATAATA | 8065 |
rs538484986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066260 | AGGCGGGAGAAATGG[C/T]GTGAACCCAGGAGGC | 8065 |
rs538578530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108019254 | CCACAGATACCAAGG[A/G]ACAACTGTACAGTAG | 8065 |
rs538584012 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108095214 | ATGATCCCAACTATC[C/T]CAGTATTCCTGGCAA | 8065 |
rs538604325 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079220 | GCAATTCTTCTGCCT[C/T]AGCCTCCCGAGTAGC | 8065 |
rs538677371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108047571 | CTAGTAGCCACTACC[A/G]TGATGGAGTAAGACT | 8065 |
rs538677426 | snp | A/G | 4.98757e-05 | 0.00499353 | intron-variant | CUL5 | GRCh38.p7 | 11:108054829 | GTGATAATTTGAGCA[A/G]TTCCCTTGATATTCT | 8065 |
rs538711009 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108089766 | TCAGTTAGGCCGGGC[A/G]CACTGGCTCATACCT | 8065 |
rs538744267 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066902 | AGTTTATGGGTTTCC[A/T]ACTGGATTGTAAGAT | 8065 |
rs538752209 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084612 | ATATACAGTGTCCAG[C/T]ATTCAGTACAACATT | 8065 |
rs538767190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108055911 | GTTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 8065 |
rs538770626 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CUL5 | GRCh38.p7 | 11:108072868 | TTTTTAAAAATACAG[A/G]ATTGAAAATTGAAAA | 8065 |
rs538875940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108074595 | GGATCACCTGAGGTC[A/G]GGAGTTCGAGATCAG | 8065 |
rs538888086 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108083596 | CGAGTTTAAGACCAG[-/T]TCAGGGCAATGTAGT | 8065 |
rs538911565 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068768 | AGCAGAGATGACATG[A/C]TATCTTCTGCCTCAT | 8065 |
rs538925808 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103986 | CAATAAGCAGATTCT[C/T]TTTTATGGGGCATGA | 8065 |
rs538940801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013869 | AGGCCGACCTGGGCA[A/G]TGTAGCAAGACCCTG | 8065 |
rs538941228 | snp | A/G | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106372 | TTTAATTTAAGAATG[A/G]GAGTCATGATGTTTT | 8065 |
rs538955181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108094720 | CAAAATCTTTATAGT[A/C]TTATTGATTTTTCAC | 8065 |
rs538957834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108075124 | AGAACTTATTTAAAT[A/G]ATTCAATTAAGTGAT | 8065 |
rs538999206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108025629 | ACTAACTGTTTCTGG[C/T]CCTGTGTGCACTCTG | 8065 |
rs539014562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017565 | CGTGATAAGAATGTT[C/G]AAGGCCGGATGCGGA | 8065 |
rs539023303 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032591 | ATGGGGTCTCTCTCT[C/G]TCTCTCTCTCTGTTT | 8065 |
rs539028284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039811 | TGCTTTTGTTGCTTC[C/T]ATAACTTTATCATGG | 8065 |
rs539051460 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069143 | ATCCCTGTAGTCCTA[A/G]CTACTCAAGAGGCTG | 8065 |
rs539076031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024812 | GAAAATCTTGGAGTG[A/G]AATGATTAAACAAAG | 8065 |
rs539076046 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014660 | CATAGCAGGAGTAAT[G/T]AAGTCTATGGGAAAT | 8065 |
rs539108659 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108065337 | GGGAGAAATTTTATT[A/C/G]TGGCTTCTATCTCAT | 8065 |
rs539160362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108026555 | TAGTCACTTCCTCCA[C/G]ATATGCGCTAGATCC | 8065 |
rs539162520 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108059072 | AGTGGCTGTTCACAG[G/T]TTTGATCATAGTGCA | 8065 |
rs539164486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033374 | CCCAAACCCGTATCT[C/G]AAGTTGTATTGTTCG | 8065 |
rs539176008 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108031951 | GCATGTTCTCACTTA[C/T]AAGTGGGAGCTAAAT | 8065 |
rs539176035 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108019931 | GTGTAGAGATCACAC[A/G]GCAAGAAAGGAAGCA | 8065 |
rs539214062 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087502 | CAAGCATGAAAATAC[-/A]ATATACTGCTGGGTG | 8065 |
rs539228275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108092998 | ATTTTTGTATTTTTA[A/G]CAGAGATGGGTTTCA | 8065 |
rs539250111 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108027302 | TCTTTGAGACAGTCT[A/C]CCCCTGCTGTCCAGG | 8065 |
rs539268424 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108067392 | CTCCTTTTAATCCTC[A/G]TTGTAACCCACCATA | 8065 |
rs539289117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108052909 | TACAAAGTTACATCT[A/G]CTTTTTGTACTAGAT | 8065 |
rs539322211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039212 | TTTAGTAGAGATGGG[G/T]TTTCTTCATGTTGAT | 8065 |
rs539328933 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108060840 | TCTCAAAAAAAAAAA[A/G]AATAAGAATCTACCA | 8065 |
rs539357427 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108013208 | TCTCTCTCAAATCAC[A/G]TTTGTTTTTCACTGA | 8065 |
rs539369723 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011612 | AAAAAAAACCACCAG[C/T]TTTTCTTTCTTTTTA | 8065 |
rs539419381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108097874 | TACTGTCATCACTCT[A/G]AACTTACATCATTTA | 8065 |
rs539467819 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108071848 | CGTGAACCACCACAC[C/T]CAGCCTGATCACTTT | 8065 |
rs539568538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018345 | CATGAGTTCCATGTC[C/T]GTGGATTCAACCAAC | 8065 |
rs539579634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011372 | TTGTGGAAATTCTGA[A/G]TCTACATCCACAGCA | 8065 |
rs539614185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099983 | ACAGGCACATGCCAC[A/G]GCACCTGGCAGCTAG | 8065 |
rs539651833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099542 | GAGATTCAGAAGGAG[A/G]GTTGAATAAATAGAA | 8065 |
rs539716481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108086722 | AGTTTTTCCTTTCTG[C/T]TTCTTTCACAATTAC | 8065 |
rs539729553 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108071395 | AGCCCACTGAGTAGC[C/T]GGGACTACAGCCGTG | 8065 |
rs539743994 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039477 | CTTAGTTGAGAACTG[C/T]TGCTCTAGATCCATT | 8065 |
rs539753929 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108058319 | AGTAGTGCAGTCTCC[A/G]CTCACTGCAACCTCT | 8065 |
rs539795643 | in-del | -/AAAAAA | 0.155656 | 0.231515 | intron-variant | CUL5 | GRCh38.p7 | 11:108040612 | GTGAGACTCCGTCTC[-/AAAAAA]AAAAAAAAAAAAAAA | 8065 |
rs539801971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043222 | CTACAGGCATGTGCC[A/C]CCATGCCCAACTAAT | 8065 |
rs539829100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108097277 | TGCCTCAGCTTCCCA[A/G]AGTGCTGGAATTACA | 8065 |
rs539829504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108045011 | CAAGTGATCTGCCCA[C/T]CTCAGCCTCCCCAAG | 8065 |
rs539861899 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050740 | TAGGTTACCTTCTGA[A/T]ATCTTTATGTTTAAT | 8065 |
rs539868476 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068853 | ATAGTTCAACAGCCT[C/T]GTTACCATATCCCAA | 8065 |
rs539883329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108058461 | CACCGTGTTAGCCAG[G/T]ATGGTCTTGATCTCC | 8065 |
rs539915133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108045706 | TTCTACAACAAAATT[A/T]AAAAAAAAATTAGGC | 8065 |
rs539923645 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108038652 | TCCACTCCAGCCTGG[A/G]AAACAAGAGCAAAAC | 8065 |
rs539930642 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071021 | AGTGGTAATCAGTAC[C/T]GTGAGGTAGGGTTTT | 8065 |
rs539938716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084820 | GGACAGATATAACAC[A/G]TGTTGGTAAGGATAT | 8065 |
rs539943384 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108078514 | CACTAAAAGTATTCT[A/G]TTACCCATAGAAGCA | 8065 |
rs539981512 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043682 | TCCCCATCTGTAAAA[A/T]AAGGATAAAATAGTA | 8065 |
rs539999955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108085417 | TAAAAGTTACCAGGG[A/G]ATGGGGAAGGGGGGG | 8065 |
rs540060726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031535 | AGTTATCCCAGCACC[A/G]TTTATTGAACAGGGA | 8065 |
rs540126141 | in-del | -/CA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108091480 | CAGATGGCTTGTGCT[-/CA]GAGTTTGAGATGAGC | 8065 |
rs540153103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024089 | TGGATCTGGCCCATG[A/G]ATTAGAAGCCCATTC | 8065 |
rs540160593 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108078054 | GACTAGGCAAATTCT[G/T]TTTGGCCAGATATAC | 8065 |
rs540198722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108092154 | AAACAAAAAAAACAC[A/G]AAGAGATACTACTTT | 8065 |
rs540235760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099081 | ACCATCTTAACTCAC[G/T]GCAGCCTCAACTCCC | 8065 |
rs540265232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030463 | ATGAACACAGAGAAA[C/T]CCCGTCTCTACAAAA | 8065 |
rs540360141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023796 | GGGTTTCAAAAAATA[C/T]AAGTATTGCTAGAAT | 8065 |
rs540418193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032098 | TGAAATAATCTGTAC[A/G]ACAAATCCCCATGAC | 8065 |
rs540446546 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105264 | CTTAATGTTTATATA[C/T]CTAATATTTATTATG | 8065 |
rs540510615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064922 | TTGAGTAGAATTGAT[A/G]TTAGTTCTACTTGAA | 8065 |
rs540554748 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108017656 | GGAGTTCAAGACCAG[A/T]CTGGGCAACATAGTA | 8065 |
rs540592056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108058761 | GTCTGAAGCCCTACT[C/T]TTACAGTTTTATTTT | 8065 |
rs540666056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069376 | CAGCCTATCTTTCTA[A/G]CCTTCTCTTCCACTG | 8065 |
rs540731206 | snp | A/G | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104393 | GGCATAATTTTGAAT[A/G]TCATGGACAATATTT | 8065 |
rs540746943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108070247 | GGTATCTTTGAAACA[A/G]ATCACTTACTAAGTT | 8065 |
rs540772135 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108063367 | TCATCCATGTTGTTG[C/T]AAATGGCAGGATCTC | 8065 |
rs540791107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108097308 | GGCGTGAGCCACTGC[A/G]CTTGGCCTGAAGTTC | 8065 |
rs540799026 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108015693 | AGTAACTGTAAAACT[C/T]TGTGATACATGTAAA | 8065 |
rs540827908 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108096839 | CCAAAATGCTGGGAT[G/T]ACAGGCCTGAGCTAC | 8065 |
rs540830076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108103962 | TATCCCTCCCCTATC[C/T]CCCCACCCCAATAAG | 8065 |
rs540960085 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105905 | GCATTTCGTAGGATC[C/T]GTCCCCATCCGAAGA | 8065 |
rs541001783 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057940 | TATTGGCTGGGTGCA[A/G]TGGCTCACGCCTGTA | 8065 |
rs541015064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015314 | TTCCTTGTAGAGGGA[A/G]CAGCCAGTGTGAAAG | 8065 |
rs541018612 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108022977 | TTCCTGGCCCAGCGT[A/G]GTGGCTCACGCCTGT | 8065 |
rs541042041 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084999 | CACTCCCACTGCTTC[A/G]CTTGACTAGCCTTTC | 8065 |
rs541060236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108062844 | CTGTTTTTGTTTTTG[C/T]TTTTGTTTTGTTTTG | 8065 |
rs541068616 | snp | A/T | 1.6832e-05 | 0.00290099 | intron-variant | CUL5 | GRCh38.p7 | 11:108095000 | ATTGTAAGTAGATAG[A/T]GTGTTAGTTATTTCA | 8065 |
rs541083171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108014155 | ATCAGTGAAAATTTT[A/G]TGGAGAAAGTGTTGG | 8065 |
rs541114348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108081908 | TGTGTGCATGTTTCA[A/G]GTTGGTTCTTTTTCA | 8065 |
rs541149639 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090662 | TAATCAATGCTGATT[A/G]TAACTAAATTCCCAT | 8065 |
rs541175517 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | CUL5 | GRCh38.p7 | 11:108035565 | AACATAGTGTGAGAC[C/G]CTGTCTCTTAAAAAA | 8065 |
rs541184591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090284 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 8065 |
rs541193088 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076841 | GATGACACTCAGATT[C/T]GTGTTCTGATCAATT | 8065 |
rs541212705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042885 | CCCTTGCCTTAGCCT[C/G]TTGAGTACCTGGGAC | 8065 |
rs541216055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108082619 | GATTGTTCCTTGCTG[A/G]TGTATAAAAACACAA | 8065 |
rs541244348 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108035455 | TCAGTAATCTTTGAC[A/G]GCCAGACAAAGTGGC | 8065 |
rs541269160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108058060 | CTAAAAATACAAAAA[C/T]TAGCCGGACGTGGTG | 8065 |
rs541277987 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108050384 | CTCTTTTTTTTTTTT[A/T]AAACTGGAGTGTCAC | 8065 |
rs541299118 | snp | A/G | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107082 | AATATTACTATTCCA[A/G]TGATTAAATGAGGAT | 8065 |
rs541300961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108075975 | GTGGCAAGAGCACCC[A/G]AAGTCTACTTAGCAT | 8065 |
rs541303024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042179 | TAGCCACATTGATGT[A/G]CTTATAGTCCACTGC | 8065 |
rs541383587 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027561 | ACATGTGTGAGCCAC[C/T]GTGCCCAGCCAAATT | 8065 |
rs541389829 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008367 | TGTAAACCTGCAAAA[C/T]ACAATACCAGGTATC | 8065 |
rs541400064 | snp | A/G | 4.51722e-05 | 0.00475227 | intron-variant | CUL5 | GRCh38.p7 | 11:108095523 | AAATCTGTTTTATCT[A/G]TTATAGATAACATTT | 8065 |
rs541403773 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108075817 | AGCCACCACCCCTGG[-/C]CCCCCTTTCCCTTTA | 8065 |
rs541438749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108101444 | TTCTAGTTGCTAAGG[A/G]CCCCATGGCCTCTTC | 8065 |
rs541446384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108104135 | ATTTTTCAGTTTGTT[A/G]TACTTAAAATAATTT | 8065 |
rs541453102 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007868 | CCTTCAGGGTTCAAG[C/T]GATTCTCCTGCTTCA | 8065 |
rs541467830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064142 | GTTTTTCTCCATTCA[A/G]TATGATACTAGCTAC | 8065 |
rs541488597 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108041645 | GCCTAGGCTGGAGTG[C/T]AGTAGCGTGATCTCG | 8065 |
rs541517918 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050973 | TTCCACTTGTAAGAA[A/T]AAAATGGGACCGTAG | 8065 |
rs541534333 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099365 | GCATATTACCTATAG[A/C]TCATGTAATAGGATA | 8065 |
rs541539443 | snp | A/G | 0.00115614 | 0.0240153 | intron-variant | CUL5 | GRCh38.p7 | 11:108088664 | TTAAAGAAGTGGTAC[A/G]TGAATTTTTTGTATT | 8065 |
rs541569260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096010 | CTGAGGCAGGAGAAT[C/T]GCTTGAATTCAGGAG | 8065 |
rs541594402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084506 | TCGATTCAGTGGCTA[A/G]CCCTGGAGATGGACT | 8065 |
rs541598481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108091346 | GTGAGCCACCACACC[C/T]GGCCTATGTTATTTC | 8065 |
rs541609648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108097386 | AGATGGTGTTTACTA[C/T]GGTCCTGTGTGACCA | 8065 |
rs541720689 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082551 | CAAAGTGCTAGGATT[A/G]CGGGCAGGAGCTACC | 8065 |
rs541803940 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108042300 | TCTCGGCTCACTGCA[A/G]CCTCCACCCCCGGGT | 8065 |
rs541829187 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108023613 | TTAAGGAACACTATA[A/C]TAGAATGTGAATTGC | 8065 |
rs541829306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108103333 | TGGGAGACCAGGGCA[C/G]GGGAGTATTTGAGTC | 8065 |
rs541841234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108057497 | GATATGATGCACTAA[A/G]AAGAATACAATATTA | 8065 |
rs541857220 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042472 | AGTGATCCACCAACT[C/T]TGGCTTCCCTAAGAG | 8065 |
rs541890156 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108042764 | TTTTTCTATCAGTTT[A/C]TTTTTTTTTCTTTTT | 8065 |
rs541904719 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089345 | TCAGGACTGGGTATT[A/T]CTCAGAGATGGATAA | 8065 |
rs541905553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108049316 | GATATACCATATATT[C/G]TGGGGTTTTTTGGTT | 8065 |
rs541908545 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066301 | GTGAGCCAAGATCAC[A/G]CCACTGCACTCCAGC | 8065 |
rs541993026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010098 | CTAGGCCCACAGGGG[C/G]AGATTCTCCACCAGT | 8065 |
rs542025002 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CUL5 | GRCh38.p7 | 11:108036262 | TCCATTGTGGAGATT[C/T]ATTCTGCTCCCAATA | 8065 |
rs542029866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108044039 | TAAATAAATAAATAA[A/G]TAGTATCTGGCACAT | 8065 |
rs542029947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037344 | CAGCAAATGTTTGTC[A/G]TCCTACTGCTTCTTC | 8065 |
rs542051840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108051726 | TTTCAGTTGGTCCTT[C/T]TTACATTTTTTATGT | 8065 |
rs542057151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108029615 | TATGATTTAATGATA[C/T]GCTCTTCAGTTTAAT | 8065 |
rs542098218 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108069945 | ACTAGTATAGCATAT[A/C]CATCTTCAATAATCC | 8065 |
rs542098567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108063499 | ATAAGTAGTGCTGCA[A/G]TACATGTATACATAT | 8065 |
rs542148341 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | CUL5 | GRCh38.p7 | 11:108016106 | TTTTTTATAGAGATG[A/G]GATCTCACCATATTG | 8065 |
rs542185702 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108046164 | TCAGACACCATTTAC[G/T]TGGTTCTAATATGGC | 8065 |
rs542194650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108022994 | TGGCTCACGCCTGTA[A/G]TCCTAGCACTTTGGG | 8065 |
rs542257704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034592 | CAGGTTGAATTAAAA[C/G]GACTCATGGCAGCTT | 8065 |
rs542301793 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020856 | AGTGTACAGTAATGT[C/T]CTAGACCTTCACATT | 8065 |
rs542306266 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108075574 | GGAAGTTCGCTGTGT[C/T]GCCCAGTCTGGAGTG | 8065 |
rs542343124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108082698 | CACCTAGGCTGGAAT[A/G]CAATGGCATGATCAC | 8065 |
rs542373208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108014405 | GAGTGAAAGGGAAGT[C/T]GGGTCAGATTACAAA | 8065 |
rs542390635 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108028220 | AATACATCTAAAACC[A/T]GTCTCACAAGCTTTC | 8065 |
rs542420840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028948 | TCCTACAAGATCCAG[C/T]TCAGTAAGATCCAGT | 8065 |
rs542539965 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009246 | CACCCTGGTGCGGGC[C/T]GACGGGCCCTGGGCC | 8065 |
rs542554629 | in-del | -/T | 0.471673 | 0.115589 | intron-variant | CUL5 | GRCh38.p7 | 11:108100105 | GAATTTTACAAATTG[-/T]TTTTTTATCAGAATA | 8065 |
rs542557358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015040 | AGTAGTTGGGATTAC[A/C]GGTGACCACCACCAT | 8065 |
rs542579660 | snp | C/G | | | intron-variant, utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108073980 | ACCATCTTTTTCCAT[C/G]CTCACTAGTATAGGA | 8065 |
rs542588128 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015735 | TTCATGTTCTATGAA[A/G]ATAAATGATTGAACA | 8065 |
rs542603013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108027651 | TGGGCTCAAGTGACC[C/T]GCCCGCCTCAGCCTC | 8065 |
rs542613845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012294 | TTGTTCCACCCCAAA[C/G]AGCAATTGTTTAAAC | 8065 |
rs542645494 | snp | A/G | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105319 | ACACAGAAATCTCCT[A/G]CTCTGATATAGTTAT | 8065 |
rs542670237 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108012345 | CCCTCTTAATTCTTA[A/G]TACATTACTTTACCC | 8065 |
rs542679527 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106812 | ACCTGCAGTTAAGTG[A/G]AAAGAAAATCCAGCC | 8065 |
rs542751038 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077404 | GTAATCCAGCACTTT[C/G]AGAGGCTGAGACAGG | 8065 |
rs542761710 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108067930 | TTCTTTATTTTTCTT[G/T]TTTTTTTCCTTTTTT | 8065 |
rs542762151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108100270 | ACTTTAGGCTCGGCG[C/T]GGTGGCTCACACCTG | 8065 |
rs542776712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108094746 | TTCACCCAAAGTTAC[C/T]CTGTATTTATTTTGA | 8065 |
rs542793126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108101597 | TCACCTTGCCCTGTC[A/G]TTAAAGGCCCTGTGG | 8065 |
rs542807006 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108021162 | AAGTACATGCTGTTA[-/T]TTTTCACACAACGAT | 8065 |
rs542822455 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007697 | ATGGAGATTAGGATA[C/T]TAGTTTCCTTTCCCT | 8065 |
rs542826391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087256 | AAAGTTTCATCCACC[C/G]CACTAAGAGTTGATG | 8065 |
rs542863447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100827 | CAAGGCCAGGAGATC[A/G]AGACCATCCTGGCCA | 8065 |
rs542898224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108054361 | AAGATTCAGTTTAAA[G/T]CCCATTGCTTCTGTG | 8065 |
rs542900682 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038430 | TGGTGGCTCACACCT[G/T]TAATCCCAGCACTTT | 8065 |
rs542928303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108055380 | TGAATAATGAATCAT[C/T]TATTCCTAGGGGATA | 8065 |
rs542954587 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008555 | TTTTTCAAACTTTTT[G/T]GTAATGACGAGGGTG | 8065 |
rs542992830 | snp | A/G | 1.67908e-05 | 0.00289743 | intron-variant | CUL5 | GRCh38.p7 | 11:108095710 | GGTTTATGTTTTTTT[A/G]TTTTTAAGACTGTAT | 8065 |
rs542995640 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107543 | CTGGAGTGTTGAACA[A/G]ATTTATTTTAGTTTC | 8065 |
rs543062303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018824 | TACTTGCAATGTAAC[A/G]ATGGTTATGAGCTCA | 8065 |
rs543066134 | snp | A/C | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108026726 | CCAGGCGCAGTGGCT[A/C]ACGTTTGTAATCCCA | 8065 |
rs543087888 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108006974 | CATCTTATTTTTTGA[C/T]ACATTTCCAAGTAAA | 8065 |
rs543137937 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108014472 | TTCTATAGTTACTGA[A/G]GAATATTTGAAAAAT | 8065 |
rs543151094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012704 | CAGGTTCAAGCAATT[C/G]TCCTGCCTCAACCTC | 8065 |
rs543164170 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009256 | CGGGCCGACGGGCCC[G/T]GGGCCCTGGTGGGAG | 8065 |
rs543176259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108068875 | ATATCCCAACCACCC[A/G]CTCCTTACCACCTGC | 8065 |
rs543226340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108015151 | TGATCCTCCCACCTC[A/G]GCCTCCCAAAGTGCT | 8065 |
rs543228904 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108047803 | GTACCACGTTTTCTT[C/T]TTATGACTTGATAAA | 8065 |
rs543274840 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085688 | AAGTAAAAGAAGTGG[A/G]TCACAAAATACCACT | 8065 |
rs543289941 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108046927 | TCTGTGACACCTTGT[A/C]ATGTTGTTTCAAATC | 8065 |
rs543297556 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108081242 | GCAGTGAGCCGAGAT[C/T]GTGCCATTACACTCC | 8065 |
rs543335340 | snp | A/C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056498 | ATTTGCAGTATGTAT[A/C/T]CTCTTTGGTTGAAAT | 8065 |
rs543362514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108009641 | TTCAAGGGACCAGCT[C/G]TGGCCGGGAGCGGGA | 8065 |
rs543365609 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108068435 | CTGACCCTCCCACCT[C/T]AGCCCCCCAACTCGC | 8065 |
rs543396304 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108021266 | GGAACTTCACAAATC[G/T]TAAAACAACTAAACT | 8065 |
rs543408361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028339 | CATTTTCTCATATCT[C/T]AGATGCTTACTGTTA | 8065 |
rs543415015 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108065797 | GTTCTTATGAAGGTG[-/T]TTTTTTTGTGTGTAG | 8065 |
rs543432622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028718 | GTGCACACCTGTAAT[C/T]CCAGCTAGGGCAGGA | 8065 |
rs543456835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108060948 | GCCTGCTGTGTTTTA[C/T]AGCAGGCATTATTTT | 8065 |
rs543475053 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108021495 | TTTAAATTTTATTCA[-/T]TTTTTTAGAGACAGG | 8065 |
rs543535415 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038549 | GTGCGGTGGTGGGCC[C/T]CAGTAATTCCAGCTA | 8065 |
rs543569812 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108096136 | ACACACACACACGAG[A/T]TATTTATGGAAAAAA | 8065 |
rs543583166 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108081319 | AAGAGTTTTATAGTT[C/T]TGACTTTTACATTTA | 8065 |
rs543617365 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108087889 | AGAATCGCTTGAACC[C/T]GAGAGGCAGAGGTTG | 8065 |
rs543632965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108041557 | GCTGGGATTACAGGT[A/G]GAGCCACCATGCCCA | 8065 |
rs543652929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042312 | GCAACCTCCACCCCC[A/G]GGTTCAAGCAATTCT | 8065 |
rs543726562 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030825 | TTATGTAATTTTATC[A/G]TGAATTTGATAAACA | 8065 |
rs543729307 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108089297 | TAACAATTTGGTTAT[A/G]GTCTCAGTTTTGCTA | 8065 |
rs543743126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108081882 | CCTTGCGATAAGCTT[C/T]AAAAGCAAGATGTGT | 8065 |
rs543750397 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089028 | AAGGGATGAATGAGA[A/G]TAGATTAAGTAGTTG | 8065 |
rs543756428 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108057197 | CCACTACACCTGGCT[A/C]ATTTTTTATTTTTTG | 8065 |
rs543772222 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036209 | TGTCTCTCTTTTTCC[A/G]GGGTCATCAGTAGTT | 8065 |
rs543782467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100890 | AAAAACTAGCCAGGT[A/G]TAGTGGTGCATGCCT | 8065 |
rs543789156 | snp | G/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032324 | CCAGCCTGGGAAATA[G/T]AACAAGACCCCATCT | 8065 |
rs543789530 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007203 | GCTGGGCTTACAGGA[C/T]TGCACCACTGTGCTT | 8065 |
rs543797905 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108053873 | TTTTTCTTTTTTTGA[G/T]ACAGAGTCTCACTCT | 8065 |
rs543801156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013461 | GTCTTCTCCTGATAA[C/G]TAGTATTCTCTCTCT | 8065 |
rs543849564 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096330 | GCAATCCCATCTCTA[-/A]AAAAAAAAAAAAAAA | 8065 |
rs543936170 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108042393 | AGGCTAATTTTTGTA[-/T]TTTTTTTTAGTAGAG | 8065 |
rs543970346 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108072541 | TTGAAAATAGTGAGC[A/G]GTTACCAGAGGCTGG | 8065 |
rs543983289 | snp | G/T | 0.0126979 | 0.078662 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007773 | TTTTTGTTTTTTTTG[G/T]TTTTTTTTTGAGACA | 8065 |
rs544021710 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108069984 | AGGTAAGTGAAATCT[A/G]CTTTCAGTATAATTT | 8065 |
rs544079304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108026062 | CAGAAGTCTCTTTCT[C/T]TTTTCACCTTGAAGT | 8065 |
rs544094577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108074769 | TGAGATCGTGCCATT[A/G]CACTCCAGCCTGGGC | 8065 |
rs544121212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108067099 | TGAACCAACTGTGCA[A/G]CATTTGGAAGTTATG | 8065 |
rs544123013 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085498 | GAAGTTCTAGAAATA[C/G]ATAGCGGTGATGTTT | 8065 |
rs544135207 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088119 | TGGATACATTTTAAA[C/G]AGTGAAATAACAGTT | 8065 |
rs544196618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108086099 | TCATAGAGCATAGAA[A/G]AGAGGGTATTAACCA | 8065 |
rs544236989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108045886 | AATAAAAAAATTTTT[A/T]AAAATAATTAAAAAG | 8065 |
rs544238138 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071086 | GTGCTTTGTAAATTG[A/C]AAAATTATTTATGAA | 8065 |
rs544243202 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108039089 | CAATGGCGCAATCTC[-/G]GGCTCACTGCAACCT | 8065 |
rs544286159 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066498 | AACTCACTCTGTTAC[-/T]TTTTTTTTTTGGATT | 8065 |
rs544291430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030984 | ACTGTTTCAGTGTTA[C/T]AATTTCAGGGAGTTT | 8065 |
rs544337900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017154 | AGCACTTTGGGAGAT[A/T]GAGGTGGGTGGATTA | 8065 |
rs544360907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087084 | TTTGTTTTGCAAATG[A/G]CTCAGGAGGTGTTCA | 8065 |
rs544384001 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | CUL5 | GRCh38.p7 | 11:108040520 | GGCCAGCTGAGGCAC[A/G]AGAATTGCCTGAACT | 8065 |
rs544424613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017733 | TGCATGCCTGTAATC[G/T]CAGCTACATGGGAGG | 8065 |
rs544475084 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107605 | CGATTTTGAATGTGT[A/G]CCACTACATACTGAG | 8065 |
rs544500475 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105944 | GAACTGCCTGCTGAA[C/T]GGAAGGAAAGCAACT | 8065 |
rs544533150 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108045135 | ATTTCTATAATGAAG[A/C]ACTTTTTTGTAAACT | 8065 |
rs544593093 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108031356 | GGCAACAGAACGAGA[C/T]TCTGTCTCAAAAAAA | 8065 |
rs544633325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087702 | TGCGGTGGCCCACGC[A/G]TATAATCCTAGCACT | 8065 |
rs544641869 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024008 | TCTAGATAATTGTCA[C/T]TAAATTTTTATAATC | 8065 |
rs544659674 | in-del | -/GGTG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017157 | ACTTTGGGAGATTGA[-/GGTG]GGTGGATTACCTGAG | 8065 |
rs544669958 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108026823 | GCGAAACCCCATCTC[A/T]ACTAAAAATAGAAAA | 8065 |
rs544684854 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108022388 | TTTTATTTTTTAACA[C/T]GATAACAAATACTGT | 8065 |
rs544753559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108067184 | CATGTGGGTTAAATG[A/C]GATCTATATGTAAAG | 8065 |
rs544845863 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108053074 | ATTTGAATGTGTAGC[C/T]CATAAAAGGTAACTA | 8065 |
rs544932687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021017 | TTTAGATACACAAAT[G/T]CTTACCACTTTGTCC | 8065 |
rs544934626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099721 | ACACCAGTCATCTTC[C/T]CATGTTTCCAGGCAG | 8065 |
rs544953008 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | CUL5 | GRCh38.p7 | 11:108042542 | TCTATATACTGTCGA[-/T]TTTTTTTTGATAAAA | 8065 |
rs544979113 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108049582 | TCCTGAGCTCAAGCA[A/G]TCCTCCCGCCTCAGC | 8065 |
rs545028089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108040117 | TTTCCTCCCTCTCCT[A/G]TTTCCCAACTCCTAG | 8065 |
rs545065876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017854 | CCTGTCTCAAAAAAA[A/C]AAAGTGTTCGGAAGG | 8065 |
rs545091346 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081922 | AAGTTGGTTCTTTTT[C/G]AAGATCATTCTGGCT | 8065 |
rs545139016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108081202 | CTGAGACAGGAGAAT[C/T]GTCAGAATCTGGGAG | 8065 |
rs545180908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108020306 | GTTACCATAGGAGAT[A/G]ACAGCCCCATTCAGG | 8065 |
rs545198640 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108047844 | GTTTATTTCAGATAG[A/G]TAGAGCTTTATTCTT | 8065 |
rs545198780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011660 | GGGGGACGGAGTCTC[G/T]CTCTGTTGCCAGGCT | 8065 |
rs545201533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099728 | TCATCTTCCCATGTT[C/T]CCAGGCAGGCTCTCC | 8065 |
rs545223304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012678 | CTCCACTCACTGCAA[C/T]CTCCGCCTCCCAGGT | 8065 |
rs545251476 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101489 | CCTGCTCTTACTGAG[C/T]TCTTGAAGCCTCTGA | 8065 |
rs545289084 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108061093 | CTCATCTCAGGCAAA[C/G]ATACAGGAGTTGATG | 8065 |
rs545329731 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108039676 | GTTTCCATCTATGAA[G/T]TTGCTTATCTAGATA | 8065 |
rs545343000 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108006793 | CCACTCCCGGCTAAT[A/T]TTTTGTATTTTTAGT | 8065 |
rs545361948 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108100964 | AACCTGGGAGGCGGA[C/G]GTTGCAGTGAGCGGA | 8065 |
rs545392001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108046047 | ATTTTATGTGGTAAG[C/T]AGCAGAGAATTAAAG | 8065 |
rs545420805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032069 | AAAATAACTAATTGC[G/T]TAATCCTGGATAATG | 8065 |
rs545425077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108025316 | GATAGTTTATATTTT[C/T]CTGTTTCTTTGCATG | 8065 |
rs545484124 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108085216 | TAAGCAAAGTATGCT[A/G]TATCCATACAGTGGA | 8065 |
rs545507129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108059816 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTAAGG | 8065 |
rs545509654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066323 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT | 8065 |
rs545543929 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108059315 | ATTATGCTAGTTGGG[G/T]ATAATAAGATAGACC | 8065 |
rs545547401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085586 | ATGATAAATCTTTTT[A/T]ACTCTTAGTAAAAGA | 8065 |
rs545547455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108077820 | TGTAGTGGTGGGCAC[C/T]TATAATCCCAGCTAC | 8065 |
rs545599612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012267 | GTGCTCATTTTTTTC[A/T]TTTCCAGTTTATTGT | 8065 |
rs545610394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108091520 | CGTGGTGAAACCCCA[C/T]CTCTACAAAAATTTA | 8065 |
rs545644169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108053215 | AGAGTATGCTTCTTC[C/T]CCACGCTTCATCCTC | 8065 |
rs545690496 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108079348 | TGACCTCAAGTGATC[C/T]GCCCACCTCAGCCTC | 8065 |
rs545697997 | snp | C/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106869 | TTAATTTTTAAAAAT[C/T]AGTGGTATGGCAATA | 8065 |
rs545707023 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108078352 | TGTTATTGTTAGTTT[C/T]GTGACTTTTGCAGCT | 8065 |
rs545714400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108094134 | TGAGCTTTGTTCTTG[A/G]GGAATTGGTATTATT | 8065 |
rs545718673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038070 | CTATCAATTAACTTA[C/T]ACTTCTTGCCTTTGG | 8065 |
rs545759751 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035289 | AATCTCCATATCAGA[G/T]ACATAAGACCAATCA | 8065 |
rs545771529 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027745 | TTCATTCCACTCTAA[C/T]CTGGTATTTGTCCTT | 8065 |
rs545772655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108036319 | TCAGCAGAAAAAAGC[A/T]AGAAATTTTGTCTCA | 8065 |
rs545789904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108097506 | TCAAATGTTATATTC[A/T]TGGAAGTACCACACA | 8065 |
rs545796225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017017 | GTACATACAAATAAT[A/G]TCAAAGGTAATTGAT | 8065 |
rs545819683 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105068 | GTTAAATGATGAGGA[G/T]TTTTTTTTTTTTTAA | 8065 |
rs545841577 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041024 | AAAGTGATTTGAGTA[C/T]GGCAGGGTTACAAAG | 8065 |
rs545856544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108029806 | TACTTAACAATGTCT[A/G]TTAGGAGATTTCAGA | 8065 |
rs545873870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108092083 | TCAAAGTTGTAATGA[G/T]CTGAGATTGTGCCAC | 8065 |
rs545886646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090196 | GACCTTATTAATAAA[C/T]AGACTACAGGGGCTG | 8065 |
rs545979311 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108031059 | AGCAATATCAACAGA[-/T]TTTGTATAACTGAAA | 8065 |
rs545988324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030423 | TGGGCAGATCACCTG[A/G]GGTCGGGAGTTTGAG | 8065 |
rs546018214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108044871 | GGTTCAAGTGATTCT[C/T]ATGCTTCAGCCTCCC | 8065 |
rs546068958 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023667 | CCCAATGCACAGTAG[A/C]GTCTCAGATGTTTGT | 8065 |
rs546088682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031444 | TTTACATTTAAGTCT[C/T]TAATCCATCTTGAGT | 8065 |
rs546199503 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108068476 | GAAAATTCTTTATTC[G/T]GAAAATTTTAAGCAT | 8065 |
rs546207699 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108016410 | AGGTGCAACACCAGC[A/C]TTCCCAGCTCATTTA | 8065 |
rs546212654 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086025 | ATAATACATATTAAT[A/G]GATAGATGGAAATTG | 8065 |
rs546277473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069476 | CTTACTTTACAGGAT[C/T]CCATTTAGATACCAA | 8065 |
rs546282016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071302 | GTCTCGCTGTGTTGC[C/G]CAACCTGGAATTCGA | 8065 |
rs546287266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084689 | AATCATTTTAGAAGC[A/G]ATCTCAGGTGATCCT | 8065 |
rs546317224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108076872 | AGAAGGATATGTTCA[C/T]TGCGATAGGGAAGAC | 8065 |
rs546323667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037574 | AAACTTCCAAATGTC[G/T]TCTCGCAGAGGAGTC | 8065 |
rs546345281 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108071608 | GCTGAGTGCAATGGT[A/G]CAATCACGGCTCACT | 8065 |
rs546373745 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106982 | TTGTGTTGCCATCTC[A/G]TTGCCGGAGTAAGTA | 8065 |
rs546447899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108088357 | TAGGGGAACGTAAAA[A/G]TGAGTGCCTCCCTAA | 8065 |
rs546459603 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060193 | AGGAGGTCTAAAATT[A/T]AAAAAAAAAATTAAG | 8065 |
rs546461520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064842 | TCTGCTTTTGGTATT[A/G]GGGCAATACTGGCCT | 8065 |
rs546477610 | in-del | -/AA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038657 | TCCAGCCTGGGAAAC[-/AA]GAGCAAAACTCCATC | 8065 |
rs546500602 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066735 | GTGTGCCAGGACACA[A/G]CACAGTCTTTATAGC | 8065 |
rs546521431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108065597 | TGGTGAGTTCAATGC[A/C]GTATCTCACAGTTGC | 8065 |
rs546612085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011262 | AAGCTACTTTGGTCT[A/C]TATTAGTTAAGTACT | 8065 |
rs546621686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108091624 | AGCCTGTGAGGTGGA[A/G]GTTGCATTGAACAGA | 8065 |
rs546645024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031197 | ACATGGCGAAACCCC[A/G]TCTCTACTGAAAATA | 8065 |
rs546775352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108057800 | AGTATCGTACCAATA[C/T]TATTTTCCTGGTTTT | 8065 |
rs546796047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108063897 | TTCTCACCAATATTT[G/T]TTATTGCCTGTCTTA | 8065 |
rs546810621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016530 | GCTGGGATTACTGGC[A/G]TGAGCTACCACCCCT | 8065 |
rs546811290 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108025510 | GTCCAGAATATCACT[C/T]GGGGTAGGGCTACTT | 8065 |
rs546825002 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050620 | TGATCTGCCTGCCTC[A/T]GCCTCCGAAACTGTT | 8065 |
rs546834248 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, splice-acceptor-variant | CUL5 | GRCh38.p7 | 11:108106205 | GCCCTTATGTTTAAC[A/C]GATAATTCAGCATTG | 8065 |
rs546847683 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043680 | TTTCCCCATCTGTAA[A/C]ATAAGGATAAAATAG | 8065 |
rs546871305 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093308 | TTTTGGGCTGTCAGT[A/G]TCATGAAATACTGAG | 8065 |
rs546930129 | in-del | -/GAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108045131 | ATATATTTCTATAAT[-/GAA]GAACTTTTTTGTAAA | 8065 |
rs546959679 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108107974 | AATGTAGCTTTTCCA[C/T]TGATGATAGCATGTG | 8065 |
rs546964155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102570 | TCCACGACTCAAACG[A/G]TCCACCCACCTCAAC | 8065 |
rs547000397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108098226 | ACAGGTTAGTTATCA[C/T]GTTTAAGGAAAATAC | 8065 |
rs547003048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108102015 | TCATATCTTTTATTT[A/G]TTTTTGTTTATTTTA | 8065 |
rs547053167 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069690 | CTTATTCTTGTCTCT[C/T]AAATACTTCCTTAGT | 8065 |
rs547071806 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008756 | TAAGCATTTCAGGAC[A/C]ATGCACCTCCCTTAA | 8065 |
rs547082363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108014693 | ATTTATTCATTGAAC[A/G]AGAATTTAGTATTTC | 8065 |
rs547084027 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108013218 | ATCACGTTTGTTTTT[C/T]ACTGACTTCCCTCCC | 8065 |
rs547113683 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072134 | CAGTGAGCCGTGATC[A/G]AGCCACTGTACTCCA | 8065 |
rs547129460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010170 | TGTTCTGTGTATGTG[G/T]CTGTAGTAGTTAATC | 8065 |
rs547130679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096196 | AGAGAAAAGTGCTTC[A/C]AAAAAAAGGAGAGGC | 8065 |
rs547135347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108103369 | GTTCAAGACCAACCT[C/G]GACAACATAGCAAAA | 8065 |
rs547148807 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108031957 | TCTCACTTATAAGTG[A/G]GAGCTAAATGATGAG | 8065 |
rs547229971 | in-del | -/GA | 0.0882795 | 0.190647 | intron-variant | CUL5 | GRCh38.p7 | 11:108061900 | TGGCAGCAGGAGAGA[-/GA]GAGAGAGAGAGAGAG | 8065 |
rs547238415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108097104 | CTCACTGCAACCTCC[A/G]TCTCCCAGGTTCAAG | 8065 |
rs547242121 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108082992 | ATTTATTGGCTCAGA[A/T]ACCTTTTTTGTAGAT | 8065 |
rs547259342 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CUL5 | GRCh38.p7 | 11:108029155 | CCCATTTGTGTGAGA[A/G]GAAGAGTGCCTGTGA | 8065 |
rs547324590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042330 | TTCAAGCAATTCTCA[A/T]GCCTCAGCCTCCCAA | 8065 |
rs547364368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108091103 | GTTACCCAGGCTGGA[C/T]TGCAGTGGTGCAATC | 8065 |
rs547430638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108041951 | TGGAATGTCTGGCAC[A/G]TAGTAAGCAGTTAAT | 8065 |
rs547436206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048092 | TAAAAAGACCCATCT[C/T]AAAAAGATTTTTAAA | 8065 |
rs547437721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087982 | AAAAAACTAAAAAAA[A/G]ATTTGTATCAGGAAA | 8065 |
rs547461193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108041014 | CATATATGCAAAAGT[C/G]ATTTGAGTACGGCAG | 8065 |
rs547463995 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108056272 | AGCCTTGATTTAGAT[G/T]TGCATTCTCAGGAAT | 8065 |
rs547475745 | snp | C/G | | | intron-variant, utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108073915 | ATGGGACTCCTTCGG[C/G]AGTTATGTTATACTT | 8065 |
rs547499710 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009292 | GCCTCCGGTCAAGGC[C/T]TGGCCGGGAGCGCCA | 8065 |
rs547509862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108088815 | GACCTCTCGGGGGGT[G/T]ATTTTTCTTTCTGAA | 8065 |
rs547515209 | snp | A/T | 3.87785e-05 | 0.00440315 | intron-variant | CUL5 | GRCh38.p7 | 11:108073539 | CACTTTTAAAAGTTT[A/T]ATTCTCATAATTTAC | 8065 |
rs547516876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108081479 | GGTTGGCTGCCAGGC[A/G]TGGTGGCTCACACCT | 8065 |
rs547538787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048892 | AGCTGGTCTCAAACT[C/T]ATGACCTCGTGATCT | 8065 |
rs547587652 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050290 | ATCTGCATCTTCAAC[C/T]ATTATCTCCTTTACT | 8065 |
rs547643574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108036643 | CCACTGTGCCAGGCT[A/G]ATTTTTGTATTTTCA | 8065 |
rs547653861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024591 | TGATTTACACATCTA[C/T]GCTGAAGATTATAGT | 8065 |
rs547685418 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053140 | AGTAAGTTACTTCCA[C/T]GAAAAGGAGAGCATG | 8065 |
rs547695887 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108055359 | TGGCTGCAAACACCA[A/C]ATTAGTGAATAATGA | 8065 |
rs547707164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108076314 | GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCC | 8065 |
rs547755292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033442 | GGTGTGGACAGTCCC[C/T]TCCCTGAATTGCATT | 8065 |
rs547773559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108080433 | ACGGGGCCTTGCTCT[A/G]TCTCCAGGCTGGAGT | 8065 |
rs547882833 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108027331 | GGCTGGAGTGCAGTG[G/T]CACAATCTTGGCTCA | 8065 |
rs547910503 | snp | A/G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086281 | AAACAGCCACGGGGG[A/G/T]AAAATAACACACTAC | 8065 |
rs547925286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068053 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 8065 |
rs547926342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090336 | TATTAAAAATACAAA[A/T]AAATTAACGAGGCGT | 8065 |
rs547989615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028488 | AGTTTTAACCCTTGC[C/T]CCTTATAATATATTC | 8065 |
rs548020131 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108027779 | ACTCTGCAAAAACTT[C/G]TGTGGACAAAGTTTC | 8065 |
rs548076617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021310 | TCAAAATGTTATGGG[C/T]GTGTAAAAGTAAGGT | 8065 |
rs548094709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108083913 | TGCGGGCTGCATGCG[G/T]CCCAGGACGGCTTTG | 8065 |
rs548102186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013959 | TTTATTGACATCCAT[A/T]TGCAAGGTACCATGG | 8065 |
rs548190467 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020933 | GCAGGCTCCATTCAT[A/G]GTGAGTGCCCAATTT | 8065 |
rs548223433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108041794 | ATGGGGTTTCATCAT[G/T]TTGGCCAGGCTGGTC | 8065 |
rs548239464 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059058 | CCAGGCTGGAGTGCA[A/G]TGGCTGTTCACAGGT | 8065 |
rs548261937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108042983 | GGCCAGGTTGGTTGC[A/G]AACTCCTGGCCTCAA | 8065 |
rs548273619 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108035074 | GTGACAGGAAAGAGA[G/T]AACTAGAGTCAGGTT | 8065 |
rs548280074 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013697 | TTAAACTGAAATATG[A/T]TTCATACTACTTTTC | 8065 |
rs548312299 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037478 | TGTATTCATGGCTAT[A/G]AATTATTACAGTGAA | 8065 |
rs548314849 | snp | C/T | 0.000798881 | 0.01997 | intron-variant | CUL5 | GRCh38.p7 | 11:108083117 | ACTAATTGCTCTGAC[C/T]GGAACGTCTACTACA | 8065 |
rs548322251 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108042362 | TTGCTGGGACAACAG[C/G]CGTGCCTCACCACAC | 8065 |
rs548333510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108062209 | TGCTTTCTGGAATAT[C/G]CTTAAATACCTCTAT | 8065 |
rs548367623 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108028566 | ACTTCAGGCCAGGTG[C/T]GGTGGATCACACCTG | 8065 |
rs548412813 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093928 | GGCTGGTCTTAAAAT[C/T]CTGGCTTCAAGTGAT | 8065 |
rs548425029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108074979 | GGAGTTAGTTTTTAC[G/T]GTGAGTAGGATGGGA | 8065 |
rs548435945 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108010378 | ATACAGGAACCTAAC[C/T]ATCATGTCTTCTTTA | 8065 |
rs548449275 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087447 | ATTTATTTACATATA[A/T]TTTTAGAGAAGTAGG | 8065 |
rs548461304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108070289 | ATTCTTTTCCACATA[A/G]GTATATGTGGAACTG | 8065 |
rs548485592 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083483 | ATGTCCTACTTTTAG[C/T]TCCACATTAAAGTAG | 8065 |
rs548491938 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108062938 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 8065 |
rs548495734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108025534 | GCTACTTTGGCTCCA[C/T]TATAGACTCAATAAC | 8065 |
rs548497094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108076930 | GGTTGCAGAGAGATC[A/C]GAAACTCGGTATTGA | 8065 |
rs548532914 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074377 | TTTTTGTATTTTTAC[A/T]ACAGACGGGGTTTCA | 8065 |
rs548538618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069673 | GAGAGCAGGAATTAT[A/G]TCTTATTCTTGTCTC | 8065 |
rs548544163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018878 | GTTGGCCTCCAGGTT[C/G]TGCCATTTGCTAGCT | 8065 |
rs548547344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108027901 | TTATTTACTTTTTGT[C/T]CAGAATACCATACTC | 8065 |
rs548558159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102732 | AATTATATTTTTAAA[C/T]GTTAAAAGCAAATGT | 8065 |
rs548578090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108019133 | TGTGCATGGGTAATA[A/G]GCAAATGCTATGCCA | 8065 |
rs548593650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108056571 | TATAGAAGTTCTTTA[A/T]AGTGATATAAATTCA | 8065 |
rs548621232 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108091226 | CTGGCTAATTTTTGT[A/G]TTTTTAGTAGAGACA | 8065 |
rs548758091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102131 | GGTTCAAATGATTCT[C/T]CTGCCTCGGACTCCT | 8065 |
rs548774266 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038816 | TTTGGCCATGTTAAT[C/T]GTTAACATTTAGGTT | 8065 |
rs548799364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108022402 | ATGATAACAAATACT[A/G]TATTTCTACACCATT | 8065 |
rs548809495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021458 | CAGCAATAATAACAA[A/C]TTCTTTGTTTCCTTG | 8065 |
rs548816890 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108100983 | GCAGTGAGCGGAGAT[C/G]GCGCCACTGCACTCC | 8065 |
rs548884654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048117 | TTTAAACGCTTAAGA[A/G]ATTTTTTTTTTTTTT | 8065 |
rs548899841 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008984 | TCGTTGCAGGTGGCC[G/T]CGGCGGGTGCAACCA | 8065 |
rs548928836 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108101001 | GCCACTGCACTCCAG[C/G]CTGGCAACAGAGCAA | 8065 |
rs548940997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108067369 | TTAATTATGTTGTCA[A/G]TTTAGCTCTCCTTTT | 8065 |
rs548952506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108092855 | AGAGTCTCACTTTGT[C/T]GCCCAGGCTGGAGTG | 8065 |
rs548952542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099805 | CTAGGTTTTCATATA[A/G]ATGGAACCAGACAGT | 8065 |
rs548956192 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108067265 | TTATAATAATTTGTT[A/T]AACCTCTCAAGCTAG | 8065 |
rs548959257 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108108002 | GTGGCTATATGCCTG[A/G]AAGAGGTAATAAAAA | 8065 |
rs549020599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100588 | CCTTACTCTGTAAGT[A/G]TAGAAGAATTTATAC | 8065 |
rs549055712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108054156 | CAGGCTTAATTTTTC[C/T]GTAGACACATGATTT | 8065 |
rs549080373 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108060704 | TACCCGGGCATGGTG[G/T]TGCGTGCCTGTAATC | 8065 |
rs549113798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108093492 | CTATAACTCCATTTA[C/T]GTTCTATTTTATTTT | 8065 |
rs549138717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048315 | ACCTAGATTAACACA[A/G]CTGTTTTATTTGTTC | 8065 |
rs549176258 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007495 | GAGTGAAAACAGGAG[A/C]TGGCAGATAACAGGT | 8065 |
rs549354933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013823 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGATGAGG | 8065 |
rs549378762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011748 | TTCTTCTGCCTCAGC[A/G]TCCCGAGTAGCTGGG | 8065 |
rs549491568 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008035 | GTGCCGATTATAGGC[A/G]TGAGCCACGGGGCCC | 8065 |
rs549508937 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025002 | CTGCTACCTCATTGT[C/T]TAATGTCTTATATCT | 8065 |
rs549512253 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108020542 | TGTTTGTGATTTTTT[G/T]TTTTTTGTTTTTTGT | 8065 |
rs549525706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108079645 | GCATAAATCTTAAGT[A/G]TACATTTGAGTCAGA | 8065 |
rs549564641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108086365 | GAGGCTGAGGAATGA[A/G]GACTGCTTGAGCCCA | 8065 |
rs549579271 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008628 | GCACTGAACAATATT[G/T]TATCTAAGTGCCAAG | 8065 |
rs549616003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108035127 | GTAACCAATCCAGAA[A/G]GGCAAACACAAGTCA | 8065 |
rs549625109 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050989 | AAAATGGGACCGTAG[A/G]TTTGAAAAGTAAAAA | 8065 |
rs549692801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066715 | TTTCTTATCAAGCAC[C/T]AGCTGTGTGCCAGGA | 8065 |
rs549694766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108073211 | CGTCTCAAAAAAAAA[A/G]AAAGGAAGAAAGAAA | 8065 |
rs549712949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095742 | CTCTCATGTAGCAGG[A/T]AATATATGATTGGCT | 8065 |
rs549731344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108072771 | CCCAATTTGATCATT[A/G]TAGTATATACATGCA | 8065 |
rs549732063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108101054 | TTGAAATGTATAAGC[A/G]GGTGTAGTCGTACGA | 8065 |
rs549757922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108061388 | CAATCTCCCTACTTT[G/T]TGCCTAGGTAAAATA | 8065 |
rs549797794 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027247 | GCCTTAGTAGCTGGG[A/G]TTATAGGCGCCACCA | 8065 |
rs549821475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108041872 | GCTGGGATTATAGGC[A/G]TGAACCACCGCACCA | 8065 |
rs549843166 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, missense | CUL5 | GRCh38.p7 | 11:108106223 | TAATTCAGCATTGGC[A/G]TATTTGCTTGTCCCA | 8065 |
rs549864864 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080725 | ATTGGATTCTTTCTC[A/T]TTGTTGTTGAGTTGT | 8065 |
rs549877766 | in-del | -/C | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108102623 | GGCATGAGCCACCCT[-/C]CCTGGCTGGTTATCA | 8065 |
rs549887736 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040964 | ACCATTCCCTGTTAT[C/G]CTATGAGACTCAAGT | 8065 |
rs549889345 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108094272 | ACAATAAAATTCTAA[C/T]AAATGAGAAAAATTT | 8065 |
rs549904533 | snp | C/T | 6.64132e-05 | 0.00576213 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054768 | GTATTTACAACAAAA[C/T]GGTGTACAGAATTAT | 8065 |
rs549908923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087429 | TCAAAATCTTCAATT[A/T]AAATTTATTTACATA | 8065 |
rs549909235 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108079704 | ATGTATGATGTCTTT[A/G]TCATCGTACAAAGTT | 8065 |
rs549967912 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108088773 | ATTATCTGTAAAGAA[C/G]TAATGTTACGAAGAT | 8065 |
rs549972286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108080646 | TGATTTGCCCGCCTC[A/G]GCATCCCAAAGTGCT | 8065 |
rs549975740 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027834 | GTGGTTATCTTACCT[G/T]ATCTGTCAGGAGAAA | 8065 |
rs550006002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108088174 | TTAAATGTTAACATA[A/G]ATATCCAAGAATTTA | 8065 |
rs550016640 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108108239 | ACCCTGTCTCTACTA[A/C]AAATATAAAAATTAG | 8065 |
rs550025038 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009572 | CTGGTGGTCGCTCCC[G/T]CCGACTGGCCGCTGG | 8065 |
rs550039634 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CUL5 | GRCh38.p7 | 11:108075117 | CCAGTTAAGAACTTA[C/T]TTAAATAATTCAATT | 8065 |
rs550051477 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031508 | GTTTTACTTTTCTGC[A/G]TATGGCTAGCCAGTT | 8065 |
rs550089977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108082818 | TTTTTTTTGAGACAG[A/G]GTCTTGCTGTGTTGC | 8065 |
rs550126452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108082345 | GAGTGCAGTGGCGCA[A/G]TCATGGCTCACTGCA | 8065 |
rs550170479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108093609 | TCATGTGGGTTTATT[A/T]CTGGAAGACAAGGAT | 8065 |
rs550171523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108027701 | CATGAACTATTGCGC[C/T]TGGCTCCTCGTTTCT | 8065 |
rs550206469 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108068007 | GATCTCGGCTCACTG[C/T]AATCTCTGCCTCCCA | 8065 |
rs550210590 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033521 | GACGTAACTTTCTAA[A/G]TGTCCAGAGATTATC | 8065 |
rs550241412 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074197 | CTATTTTAATTTTTT[A/T]TTTTTTTTTTTTTTG | 8065 |
rs550253075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108040260 | CGAGGCTGGAGGATT[A/G]CTTGAGGCCAGAGTT | 8065 |
rs550318183 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108077983 | AACAACAACAAAAAA[A/C]CCTCACTTGAGAATA | 8065 |
rs550321126 | snp | C/T | 0.000190317 | 0.00975307 | intron-variant | CUL5 | GRCh38.p7 | 11:108073508 | ATAAGGTATATATTC[C/T]TATATATATAAAAAA | 8065 |
rs550325160 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108027246 | GGCCTTAGTAGCTGG[G/T]ATTATAGGCGCCACC | 8065 |
rs550325624 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059628 | TCACGCCTGCAATCC[C/G]AGCACTTAGGGAGGC | 8065 |
rs550336561 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064137 | TTTTAGTTTTTCTCC[A/G]TTCAGTATGATACTA | 8065 |
rs550414874 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108019888 | AGCCTGCTTCTACTC[A/G]TGGCAGAAGGTGAAA | 8065 |
rs550482056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099415 | AATGAATAAAAACCA[A/G]TTGCATTTCTATGGG | 8065 |
rs550487157 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108067360 | CAGTTTACTTTAATT[A/G]TGTTGTCAATTTAGC | 8065 |
rs550490286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018909 | GTGTGGTATTGGGCA[A/G]GTTACTTAACATCTC | 8065 |
rs550494596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108060787 | GGTTGCAGTGAGATC[A/G]CGCCATTGCACTCCA | 8065 |
rs550573195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108016207 | GGAATGAGCAAAAGA[A/G]CTAGTCAGCCAGAGA | 8065 |
rs550581057 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037951 | TCAATGAATTATAGA[A/T]GTATAATTGCATAAG | 8065 |
rs550607011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085685 | GCTAAGTAAAAGAAG[C/T]GGGTCACAAAATACC | 8065 |
rs550686193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071687 | AAGTATCTGGGACCA[A/C]AGACATGCACCACCA | 8065 |
rs550698850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010307 | TGAACCACTTCTTCC[C/T]GAGGCCTCTCATGCC | 8065 |
rs550756639 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108097811 | AATTTTAGCACTTTG[C/T]TTTTTGCAAAATAAT | 8065 |
rs550776478 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106882 | ATTAGTGGTATGGCA[A/G]TAAGACACTTCAGAG | 8065 |
rs550785981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010892 | TTGTTTTAGATACAT[G/T]AATTTAATCTTCACA | 8065 |
rs550787524 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108051537 | GTATAGAATGAGTGT[C/T]ATAAAACTGTTAACT | 8065 |
rs550799823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108058404 | CAGGTGCCCACCACC[A/G]CACCCGGCTAATTTT | 8065 |
rs550813562 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, missense | CUL5 | GRCh38.p7 | 11:108106231 | CATTGGCGTATTTGC[A/T]TGTCCCAATACAAGA | 8065 |
rs550816769 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108038314 | AGAAAAGGAGCATAG[C/T]CCTACTAAAGGGGAC | 8065 |
rs550919423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012392 | CTTAACTTCCTTGGT[C/T]GATACCAAACATTTT | 8065 |
rs550953810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064445 | GGGCTCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 8065 |
rs550979099 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070245 | GGGTATCTTTGAAAC[-/A]AAATCACTTACTAAG | 8065 |
rs551004417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108025636 | GTTTCTGGCCCTGTG[G/T]GCACTCTGCTGATTG | 8065 |
rs551009810 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105335 | CTCTGATATAGTTAT[A/G]TAACTGATCTCTTAA | 8065 |
rs551047809 | in-del | -/ATTA | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108097906 | TTGTTTATGGAAAAT[-/ATTA]ATCAGATGTTTACTT | 8065 |
rs551069757 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108018415 | CGCATGCCTATAATC[C/G]CAGCACTTTGGGAGG | 8065 |
rs551160399 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016455 | GACAGGGTTTTGCCA[C/T]GTTGTCCAGGCTAGT | 8065 |
rs551197107 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108053544 | GACATTAAACTTCAC[A/T]TGCAGAGTTTTGAAA | 8065 |
rs551223943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108047224 | CGAGAGGCTGAGGCA[A/G]GAGAATTGTGTGAGC | 8065 |
rs551278127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012901 | TGCACTCTGCCTCCT[C/T]ATACAAACTTGTACT | 8065 |
rs551287007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108054071 | GGCTGGTCTTGAACT[C/G]CTGACCTCAAGTAAT | 8065 |
rs551312572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108043658 | TCTTGGATTGTTTTT[C/T]CTTCAATTTCCCCAT | 8065 |
rs551344824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085357 | CATGAATATGGTTGT[A/G]TGAGGTATCAAGAAC | 8065 |
rs551346974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108072634 | AAGTTTTGGTGTTCT[A/G]TTACCCATTAGGGCG | 8065 |
rs551352642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108011034 | TTTGTTTTATTTCTG[A/G]AGACTCCTATTAATG | 8065 |
rs551375249 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105565 | AACATTTTTTAAATC[A/G]TCAGAAGGCAACATT | 8065 |
rs551380091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108019525 | ATAATGGTGGTCTTA[A/T]AGGATTATAATGGGA | 8065 |
rs551386700 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095072 | CTTAAACAAAATAGA[G/T]TTTTGCCTCTCTCAC | 8065 |
rs551404749 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077262 | TTTCAGGAGGAGGGT[A/G]TGATCCGCTGTTTTT | 8065 |
rs551425492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018988 | TCAGAAAAAAATTGC[A/G]TCTGTATTGAATATG | 8065 |
rs551502303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108099218 | CCATGTTGCCCAGGC[C/T]GGTCTCGAACTCCTG | 8065 |
rs551558031 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108012509 | CCCAGGACTTGGTGG[C/T]ATGTCCCCTCTTACT | 8065 |
rs551580809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108100411 | AGCCAGCTGTGGTGG[C/T]GCATGCCTGTAATCC | 8065 |
rs551589818 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031061 | GCAATATCAACAGAT[A/T]TGTATAACTGAAAAA | 8065 |
rs551621355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108091799 | AGATAGACAGATGGC[C/T]AATAAGTGCATGCAA | 8065 |
rs551646587 | in-del | -/TGT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108046929 | TGTGACACCTTGTAA[-/TGT]TGTTTCAAATCAGCC | 8065 |
rs551654460 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108021306 | GTGTTCAAAATGTTA[C/T]GGGCGTGTAAAAGTA | 8065 |
rs551671218 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077880 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 8065 |
rs551734557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038421 | GGCCAGGTGTGGTGG[C/T]TCACACCTGTAATCC | 8065 |
rs551740480 | snp | C/T | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105673 | TTTAGGACTTGAGGA[C/T]GTGAACAACTTGAAA | 8065 |
rs551801862 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051020 | ATGCCATTTGAACTT[C/T]AGTCAATTTACTGTT | 8065 |
rs551855616 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059884 | GCGAGACTCTGTCTA[-/A]AAAAAAAAAAAAAAT | 8065 |
rs551878004 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108076535 | ATAAGTGAGATCATG[C/T]AGTATTTTTCTTCCT | 8065 |
rs551913661 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043046 | AGGATTAAAGGCATG[A/T]GCCGCCATGCCCGGC | 8065 |
rs551914183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085858 | TGGGGTAATGAAAGT[C/G]TTCTAAAATTTTATT | 8065 |
rs552009303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085424 | TACCAGGGGATGGGG[A/G]AGGGGGGGATGGGAA | 8065 |
rs552029164 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108097458 | TTTCTCATAACCAAC[A/T]CTTTTCACCTCTTCT | 8065 |
rs552036313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108070414 | TAGCTATCAACATCT[A/G]TGTATGTGTATGGTG | 8065 |
rs552092979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071934 | ATGATCCCAGCACTT[C/T]GAGAGACCAAGGCGA | 8065 |
rs552128780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108029080 | GGCTGCTTTCTCTGC[C/T]TAGAATACCCTTTTT | 8065 |
rs552129647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108078761 | TTGATGTGCTTCTAG[C/G]TAAGAATTACCATTT | 8065 |
rs552152997 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108016801 | ACAAAAACAAACAAA[A/C]AAAAACAAACAAAAA | 8065 |
rs552190319 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108035686 | AGATTGCTTGCTGCA[C/T]TGAGGCTGCAGCAAG | 8065 |
rs552242053 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081414 | TTTGCATGTGGATAC[A/C]CAATTGTTCCAGCAT | 8065 |
rs552252672 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083348 | GATGTGTTGCTATTA[C/T]TGTTAGTGCTACAGA | 8065 |
rs552256652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108030152 | CAGGCATAAAGTTAT[C/T]GTACAAAGTATATGC | 8065 |
rs552315345 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108058885 | GAACAGAAATGTATT[C/G]AATGTATTTAATGTA | 8065 |
rs552315478 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108036924 | AGCTAGTCTGAAGAA[A/G]CAGCTGGAGTGGTTC | 8065 |
rs552316686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108056611 | TACATTCAGAAGGCC[A/G]GGAAGGCTGTTGACT | 8065 |
rs552353223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108022533 | TTTTTTTAAGCAGTG[A/G]TATGTTCTAGAAAGA | 8065 |
rs552369330 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064443 | CTGGGCTCAGTGGCT[C/G]ACGCCTGTAATCCCA | 8065 |
rs552426825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069053 | TGAGACCAGGAGTTT[C/G]TGACCAGCCTGGGGA | 8065 |
rs552432809 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025041 | TAGTTTTTATCAAAT[G/T]AGAAAACATTTTTGC | 8065 |
rs552443974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108030601 | GAGATCGTGCCACCG[C/T]GCTCCAGCTTGGGCA | 8065 |
rs552452440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108057752 | ATTAGTGGAAAAACT[A/G]GTGAAATGAATAAGA | 8065 |
rs552469127 | snp | A/C | | | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108107863 | TAAATTTGAAGGTAA[A/C]TTAATCTCAGCCAGC | 8065 |
rs552495771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068747 | AATAATTACATGACA[C/T]GAGGGAGCAGAGATG | 8065 |
rs552524297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021592 | CGAGCTTAAGCAGTG[C/G]TCTTGCCTCAACCTC | 8065 |
rs552556348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069387 | TCTAGCCTTCTCTTC[C/T]ACTGTCTGTTTCTTC | 8065 |
rs552657475 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099256 | GCAATATGCCTCCCT[C/T]GGCCTCCCAAAGTGC | 8065 |
rs552683526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108070513 | ATAGATTAGAACCAG[C/G]TATTTGACTTTTGTG | 8065 |
rs552717977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096530 | TTGAGTTGGTATTTA[A/G]GTGTTACCTGTGAGG | 8065 |
rs552727990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015893 | GAAAGAGGATACTAG[A/G]CATCTTTCTAGTAAA | 8065 |
rs552746204 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068087 | GCACCCACCATGCCC[C/G]GCTAATTTTTAGTAG | 8065 |
rs552748500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108097964 | TTTGGTCTCTGACAT[C/T]ATACTGTATTGCATT | 8065 |
rs552763930 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108103973 | TATCCCCCCACCCCA[A/G]TAAGCAGATTCTCTT | 8065 |
rs552765337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034101 | ACAGGACTGAACATA[A/C]AATCATACTCACAGC | 8065 |
rs552781261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108097309 | GCGTGAGCCACTGCA[C/T]TTGGCCTGAAGTTCC | 8065 |
rs552783501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108061852 | AACTTAAAATCATGG[C/T]AGAAGGCAAAGGGGA | 8065 |
rs552793880 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043978 | CAGTGAGCCAAGGTG[A/G]CGCCATTGCACTTCA | 8065 |
rs552810047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108091302 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTAC | 8065 |
rs552821476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102862 | GTGCAGTGGTGTGAT[C/T]TCAGCTTACTGCAAC | 8065 |
rs552825053 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108064091 | GTGACAGTGGGCATC[C/T]TTGTCATGTTTGAGA | 8065 |
rs552831938 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060946 | GTGCCTGCTGTGTTT[C/T]ATAGCAGGCATTATT | 8065 |
rs552836975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108049734 | TGTGAACATTCGTGT[A/G]CAAGTTTTTTTGTGA | 8065 |
rs552901136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010036 | GCGCAGGAAAGTTAC[C/G]TTGTCAAAGACAGTA | 8065 |
rs552905799 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014667 | GGAGTAATTAAGTCT[A/G]TGGGAAATACATTTA | 8065 |
rs552931880 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108009818 | TCCATTTCTGTTCTC[A/G]TTCTGTCTGCACGAA | 8065 |
rs552981669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030210 | TTCCCAGTAGCCAAC[A/G]CTAAGAGGAGTGCGA | 8065 |
rs552990785 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038038 | ATTTCCGAAATGATG[A/T]AGGACCTTGCTGCAT | 8065 |
rs552991242 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023554 | AAAAAGAAAAAAAAC[A/T]AAGAATATATCCTGG | 8065 |
rs553026781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064603 | TAATCCCAGCTACTC[C/G]GGAGGCTAAGGCAGG | 8065 |
rs553057677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108049124 | CTAAAAAGAAATCCT[A/T]TACCTATGAACAGTC | 8065 |
rs553077278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016314 | CTCTGTCCCCCAGTC[A/T]GGAGTACAGTGGCGC | 8065 |
rs553079038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023982 | CGTAGTGATGTTTCC[A/G]CCGTATGGTTTCTAG | 8065 |
rs553088852 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009179 | GAGTGAGGAAGCTCC[C/T]GGTGCTTGGGACGAG | 8065 |
rs553102070 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108058509 | CGCGGCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 8065 |
rs553128882 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108010420 | TTTGATTGTCTAATA[G/T]ATGGGACTGTCTCAT | 8065 |
rs553182478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042586 | ATTTTTGTACACCTT[C/T]GCCTGGCAAACTCCT | 8065 |
rs553258015 | in-del | -/CAA | 0.0182019 | 0.0936463 | intron-variant | CUL5 | GRCh38.p7 | 11:108081287 | AGTGAGACTTCGTCT[-/CAA]CAACAACAACAAGAA | 8065 |
rs553298839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108075977 | GGCAAGAGCACCCAA[A/G]GTCTACTTAGCATGA | 8065 |
rs553299946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043996 | CCATTGCACTTCAGC[A/C]TGGGCAACAAGAGTG | 8065 |
rs553374612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095259 | TGAGGGTAGCTTACA[A/C]CTTTCATTAGGGACA | 8065 |
rs553379499 | snp | A/C | | | synonymous-codon | CUL5 | GRCh38.p7 | 11:108070174 | CAAGGCATGATCAAG[A/C]GAAATGAAACTGAAA | 8065 |
rs553394307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108089228 | TGATTTTTTTCATGT[A/C]AAGTATATCGTTGCA | 8065 |
rs553401462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108103030 | CAAACTCCTGGACTC[A/C]AGCAATCCACCCACA | 8065 |
rs553403529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096053 | GTGAGCCAAGATTGC[A/G]CCACTACACTCCAGC | 8065 |
rs553439568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108056841 | GAGGTGGAACATTGT[A/G]TCACATGGATGGGGC | 8065 |
rs553473746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108088344 | CAGCATCAGCACTTA[A/G]GGGAACGTAAAAGTG | 8065 |
rs553503732 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043928 | CTTGGGAGGCTGAGG[C/G]AGGAGAATCATTTGA | 8065 |
rs553533964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021120 | AGCCTAAGTGTATAG[C/T]AAGTAGTCTCTACCA | 8065 |
rs553543420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034466 | ACTGTTGACCATTCA[A/G]GTTCTCAGATGCCAG | 8065 |
rs553595270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028114 | TGACTTCAAGTTTTT[A/G]TTTTCTGATAGGCCT | 8065 |
rs553604762 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075947 | ACTCATTTTCTTGTT[C/T]TGTTTTGTTTTTGTG | 8065 |
rs553632281 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108081762 | GTCTCAAGAAAAAAA[A/T]CAGTTGGCTATGATG | 8065 |
rs553750250 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108022441 | GCTCCTTTACTCATG[A/G]CCTAGTAAAGTGGGA | 8065 |
rs553751953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087730 | ACTTTTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 8065 |
rs553753508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108079905 | TTGAAATTCTTTTAT[A/G]TTTTGGCATGTAACA | 8065 |
rs553755409 | snp | A/C/G/T | 5.11814e-05 | 0.00505853 | intron-variant | CUL5 | GRCh38.p7 | 11:108072324 | ATGAATGTGTTCTCT[A/C/G/T]CTTCCAGAATTACAT | 8065 |
rs553763763 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108040572 | AGCCACGATTGTGCC[A/C]CTGCACTCCAGCCTG | 8065 |
rs553786849 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035866 | GAGTGTCAGGTTTCA[C/G]CCTAGCCTCAGATCC | 8065 |
rs553788295 | snp | C/T | 6.70376e-05 | 0.00578915 | intron-variant | CUL5 | GRCh38.p7 | 11:108073530 | TATAAAAAACACTTT[C/T]AAAAGTTTTATTCTC | 8065 |
rs553818772 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108084383 | AATGTAGTTTTGGCC[G/T]AGGCTAAGCAATACT | 8065 |
rs553822966 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107397 | ACAGAAAGATTTGCT[A/G]TCTTAAACTCAAGCT | 8065 |
rs553851747 | snp | A/G | 1.6501e-05 | 0.00287232 | intron-variant | CUL5 | GRCh38.p7 | 11:108033914 | TTGATCTGTTTTCGT[A/G]AGTACCCCACTAATT | 8065 |
rs553895657 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052469 | ATTTTGCCCTGCTGC[C/T]CAGGCTGGTCTTGAA | 8065 |
rs553937483 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108006834 | TTTCACCATGTTGGC[C/T]AGGCTGGTCTTGAAC | 8065 |
rs553976857 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108075184 | AGGTGGTCAAAAGTA[G/T]TTCGATAATTTTTTT | 8065 |
rs553977079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068261 | TATACATGGATATAT[A/G]CATTTAAAAGTCATC | 8065 |
rs553977941 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051210 | AATTTGTGCCAAGGG[-/A]AAAAAAAAAGTGAAA | 8065 |
rs554004823 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108014317 | GCTGTGTTAGATATT[C/G]TATATGAATAGTGTT | 8065 |
rs554065973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108061751 | CATTTTCACACTGCT[A/G]TAAAGATAACTACCT | 8065 |
rs554073870 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007573 | GTGTTTCCAGAACAA[A/G]TGAGTTAGGAAAATT | 8065 |
rs554079039 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108016327 | TCTGGAGTACAGTGG[C/T]GCAGTCACAGCTCCC | 8065 |
rs554138185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068811 | GATGGCCTCCTAGAG[C/T]ACTAGACCCTTGCTA | 8065 |
rs554154543 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083885 | GATGTTCTAGAACAA[G/T]CTTGTCCAACCCTGC | 8065 |
rs554163604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108089065 | TCTTTGTCACCCAGT[C/T]GTTAGTGTAATGATG | 8065 |
rs554191025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108026584 | CCCATTCCCTCTTGC[C/G]TATCCAGTGCAATTT | 8065 |
rs554231699 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108060307 | GAAAGGCCAGGAAAT[A/T]AATTATTGAATACAT | 8065 |
rs554252391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108025890 | CCTTGTGATGAGGCC[C/T]GGAGACACTCTCTAG | 8065 |
rs554254912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108082451 | ACACCTGGCTATATT[A/G]TTTTTTGTAGAGACA | 8065 |
rs554272364 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108066935 | TTGAGGGCATGAACC[A/T]TGTTTATACTTCTCT | 8065 |
rs554318893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015073 | TCGGCTGATTTTTGC[A/G]TTTTTAGTAGAGATG | 8065 |
rs554351954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012682 | ACTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 8065 |
rs554406967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015595 | GAGATGGTTGCATTC[A/G]ACACAGCCTAGGGAG | 8065 |
rs554508473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021926 | CCCAAGCAGTTGTCC[C/T]GCCTCAGCCTCTGGA | 8065 |
rs554513355 | snp | A/T | 0.00159712 | 0.0282137 | intron-variant | CUL5 | GRCh38.p7 | 11:108067740 | TTGTCTTTGTTCTCT[A/T]TTAGTTATATATTGT | 8065 |
rs554526903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108081632 | TGGCGGGCACCTGTA[C/G]TCCCAGCTACTCGGG | 8065 |
rs554545414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108057178 | CTGGGACTACAGGTA[C/T]GTGCCACTACACCTG | 8065 |
rs554635428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034653 | GAAAAGGGGGAAAGC[C/T]TTCAGGACTAGTTGT | 8065 |
rs554639770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108061547 | CCCCCATACCCAGTC[C/T]TCCAGATTCAACAGT | 8065 |
rs554676835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108060926 | TTCAACAGGTACTTA[C/T]TGGAGTGCCTGCTGT | 8065 |
rs554708341 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087945 | ACTCCAGTCTGGGGG[A/C]CAAGAGCAAAACTCC | 8065 |
rs554714235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108027404 | AGCCTCCTGAGTAGC[C/T]GGGATTACTGGGGCC | 8065 |
rs554722974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108035307 | ATAAGACCAATCAGC[A/G]GCTTGATTTTGGATA | 8065 |
rs554726267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108022758 | TTTGAGATATAAATT[G/T]TTTAACTTTCTCTGA | 8065 |
rs554732298 | snp | A/G | 0.00874735 | 0.0655527 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106556 | TTTTTTTTTTTTTTG[A/G]TTATGTATACAAAAG | 8065 |
rs554739890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095364 | TGGAAAGCTGGGAGA[G/T]GAGCGTGTATTCTGG | 8065 |
rs554778163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108062454 | TCCTACCAATCTGCC[A/G]GTATCATAGATTTTA | 8065 |
rs554799291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095850 | CCTGTAATCCCAGCA[C/T]TTTGGAAGGCCGAGG | 8065 |
rs554814929 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068854 | TAGTTCAACAGCCTC[A/C/G]TTACCATATCCCAAC | 8065 |
rs554890586 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041880 | TATAGGCGTGAACCA[C/T]CGCACCAGGCCCCAT | 8065 |
rs554896390 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108101253 | ATATTGAGTGTGAGA[C/G]GGATTTGCTTGACTG | 8065 |
rs554942136 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108012586 | GAAAGTTCATATGTC[A/G]CGTCATATAAACTTT | 8065 |
rs554989181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108020035 | TGCTCACCACCCTGC[C/T]CCCACCCCCACTGGC | 8065 |
rs555017111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100862 | GGTGAAACCCCGTCT[C/G]TACTAAAATACAAAA | 8065 |
rs555020479 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108060202 | AAAATTAAAAAAAAA[A/C]ATTAAGCTTGGTGTT | 8065 |
rs555023153 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057996 | CAGGCAGATCATGTG[A/G]TCAGGAGTTCAAGAC | 8065 |
rs555025340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108054386 | TCTGTGAATGTTTTC[C/T]TGATTATTCAGTTAG | 8065 |
rs555035943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108046598 | TTTAATTAAAAGATG[A/C]TATAGCGAATTCAGT | 8065 |
rs555066468 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108065049 | ATTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 8065 |
rs555091898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033075 | TTGTACCCATAGTTA[C/T]GATTTGTTATAGGGA | 8065 |
rs555102607 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107113 | CTTGAAATAAATTCT[A/G]AAGTCTTCCAATTTT | 8065 |
rs555146019 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007707 | GGATACTAGTTTCCT[C/T]TCCCTTCCTACGCTC | 8065 |
rs555171598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039903 | TTAGTGGTTGCCTTC[A/G]TGTTTCTTGGTCTTA | 8065 |
rs555176043 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040337 | TTAGCCAAGGCTGGG[A/T]GTGGTGGCTCATGCC | 8065 |
rs555214121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013981 | GTACCATGGAGAATG[C/T]AAAGATATGTAGAAC | 8065 |
rs555239448 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108014899 | CTTATTATTATTATT[A/T]TTTTTATTTTTATTT | 8065 |
rs555258190 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108062236 | CTATCTTTTTAACAT[C/T]CTTGTGTATACATCT | 8065 |
rs555259469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108040404 | ATCACCTGAGGTCAG[G/T]AGTTCGATACCACCC | 8065 |
rs555291006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108072998 | ACAAGGTCAGGAGAT[C/T]GAGACTATCCTGGCT | 8065 |
rs555311702 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108053023 | TGCCATTAATTTCTT[G/T]GCAAGTCGTTTTAGT | 8065 |
rs555352646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011984 | TGTCTGTTTAAAGCA[A/G]GTGGACTATTGCTGG | 8065 |
rs555396283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108093071 | TCCACCCGCCTCAGC[C/T]TCCCAAAGTGCTGGG | 8065 |
rs555419199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108080924 | TTTGCTTTTGGTTTG[G/T]TTTCATATTTAGATC | 8065 |
rs555436895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108099680 | TATGTGAACATTACC[C/T]AATTAAGATACAGAA | 8065 |
rs555528761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108025749 | AGCCACAGGCCTCAG[A/G]GACCTTCTGTATAGA | 8065 |
rs555575125 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079007 | TAAACTGTGAAATAT[C/G]TGAAACATATAGCAC | 8065 |
rs555583447 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108087605 | TCTGAATTTAAAAAA[A/T]TTTTTAATTTGTGTA | 8065 |
rs555589091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108026728 | AGGCGCAGTGGCTCA[C/T]GTTTGTAATCCCAGC | 8065 |
rs555612730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018495 | AACATGGTGAAACCC[C/T]ATCTCTACTAAAAAA | 8065 |
rs555648818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032691 | GATTATGAGGTCTGA[C/T]TGTTTTGATATGACA | 8065 |
rs555685778 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080398 | CCAGGCCTTTTGCCC[A/G]TTTTTTTTGGTTGTT | 8065 |
rs555688645 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108079077 | CTTCTCTTTCACCCT[A/G]GCATTTTTTGTATTA | 8065 |
rs555714587 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108085428 | AGGGGATGGGGAAGG[C/G]GGGGATGGGAAGTTA | 8065 |
rs555830735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108044760 | TTTTTTATATTTTAA[C/T]TTATTATTATTATTT | 8065 |
rs555844086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108039979 | TCATTTTATCACACC[A/G]GGGTCACACTATTTC | 8065 |
rs555850099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038496 | AGTTCGAGACCAGCC[C/T]GGCCAACATGTCTAC | 8065 |
rs555854370 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026717 | ATTATTTGGCCAGGC[G/T]CAGTGGCTCACGTTT | 8065 |
rs555865863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074125 | CCCAAGTTTGAATGA[C/T]TCTAAAAAGACAACT | 8065 |
rs555867689 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108094628 | AGATGTTATGAAGTC[C/G]ATTTCCGTGGAGACA | 8065 |
rs555924808 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108016072 | GACTACAGGCACATA[C/T]CACCCTAGGTCTGGC | 8065 |
rs555967526 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108065473 | GAACTCAAGTCCTTA[A/C]CACTGGAATGGGCGA | 8065 |
rs555980582 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070443 | TGAATTTCTACTTTT[A/T]TCTCAAAAGCAAGAC | 8065 |
rs555995506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108027945 | CACCTGTGCTCTGGT[A/T]GCTCTCTTTGTCTCC | 8065 |
rs556002791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108053606 | TTTAACCCATATGGT[A/G]TTCATAAGATTAATG | 8065 |
rs556005385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059708 | ACGGTGAAACCCTGT[C/T]TCTACTAAAAAAAAA | 8065 |
rs556041990 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108044286 | TTTGTGAGGCTGAGG[C/T]GGGTGGATCACTTGA | 8065 |
rs556052405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034382 | TGTACCAAAATCAGT[G/T]TAAACCATATTGTTT | 8065 |
rs556128673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066238 | TGTCCCAGTACTCAG[G/T]AGGCTGAGGCGGGAG | 8065 |
rs556142536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108093974 | TCCCAAAGTGCTAGG[A/G]TTACACACCATGCCA | 8065 |
rs556175762 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103444 | TAAAAACATTTAATT[A/G]AGTCAATATAAACTG | 8065 |
rs556175991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087121 | TGAATGATATAATAA[G/T]AAAAACATATTCTAG | 8065 |
rs556286458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108073789 | GAATTCCTATTCATC[C/T]TTCCATTAAGACCCA | 8065 |
rs556330212 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107220 | TTAAACCTTCCAAAA[A/G]TGAAATGTTAGCTTT | 8065 |
rs556365098 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029917 | ACTATATTTAATTTT[A/G]TAAATTAGCAAAAGT | 8065 |
rs556366947 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106536 | TGTAAATGTACAGTT[C/T]TCTTTTTTTTTTTTT | 8065 |
rs556404603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108012594 | ATATGTCGCGTCATA[C/T]AAACTTTTCTTTTTT | 8065 |
rs556437657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108027461 | ATTTTCAGTAGAGAC[A/G]GGGTTTCACCATGTA | 8065 |
rs556463303 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101240 | GTGGCATCTGGATAT[A/G]TTGAGTGTGAGAGGG | 8065 |
rs556486404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108079303 | TGGAGACGGGGTTTC[A/G]CCATATTGGCCAGGC | 8065 |
rs556490370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108072844 | TTGATTACAAATAAA[A/G]ACATTAAATTTTTAA | 8065 |
rs556518710 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108026510 | ACCAGCACCTACATG[G/T]ACATTCTTTTGCCTT | 8065 |
rs556636894 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108062000 | GGGGGAAACCTTGCT[A/G]ATCCAATCACCTCCC | 8065 |
rs556644154 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108072258 | ACTATTAACATTACA[A/G]ACTTAACTAATGTTT | 8065 |
rs556673847 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104906 | CGGCAGATGTAGGTG[A/G]GAAGTTAAGTATTTA | 8065 |
rs556673954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108065272 | TCATGATCTGCCCAC[C/T]TCTGCCTGGCAAAGT | 8065 |
rs556737117 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108098043 | GAGAAAGCGTTTTTT[A/G]TGTTGTTTTGTTTCG | 8065 |
rs556769371 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108059809 | GAATCGCTTGAACCC[A/C]GGAGGCGGAGGTTGC | 8065 |
rs556776440 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084362 | TAAGGAGACGCAGCA[A/G]CTGAGAATGTAGTTT | 8065 |
rs556830268 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108062475 | ATAGATTTTAAAATA[-/T]TTTTTGTGTGCATTT | 8065 |
rs556927138 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059462 | AGGGAGGGAGTGTAT[C/T]ACAGTGGTTAGGGTC | 8065 |
rs556932930 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108060244 | GGTGATCCAGACTTT[C/T]GTAGTGCCACTAATG | 8065 |
rs556935903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108009918 | CCTCCTAATTCTCCC[A/G]TTCTTGAGTTCATCT | 8065 |
rs556954678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024038 | CATAGATCTTTGCAG[C/T]TTACTCTCTAAGCCT | 8065 |
rs556964026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108045502 | AGGCAGGGGGATCCC[G/T]TGAGCACAGGAGTTT | 8065 |
rs556973644 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105829 | TATGGTTTTTGAAGA[C/T]AGTAGGAAATGGAGT | 8065 |
rs557016790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108092929 | TCAAGCGATTTTCCT[A/G]CCTCAGCCTCCTGAG | 8065 |
rs557022079 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007394 | TGTATTATGTGCCTG[C/T]GCTATTTTTAAGAAA | 8065 |
rs557036021 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108042802 | GAGTCTTGCCCTGTT[G/T]CCCAGGCTGGAGTGC | 8065 |
rs557053089 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015289 | CAAGTCATGTACATA[C/T]TTAGAAGAGTTCCTT | 8065 |
rs557058765 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108010478 | GCAGTACTGTATATC[A/G]CCTTTTAAAAGGGAG | 8065 |
rs557081204 | in-del | -/AAGT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011528 | TAATATTTTGAAAAA[-/AAGT]AAGTGACTCAGTGAC | 8065 |
rs557084342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108052254 | GGGATTAGACCACAC[A/G]CAGTCGACCCTTCTT | 8065 |
rs557094112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096766 | AGACGGGGTTTCACC[A/G]TGTTGGTCAGGCTAG | 8065 |
rs557127081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108040799 | AAAAAAAAGTACATT[A/G]AGAACATTCTTCCCT | 8065 |
rs557158019 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056564 | GGTTATTTATAGAAG[C/T]TCTTTATAGTGATAT | 8065 |
rs557160242 | in-del | -/TTT | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108089233 | TTTTCATGTAAAGTA[-/TTT]TATCGTTGCATTTTA | 8065 |
rs557162782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037090 | CACCTTTGGGAACTT[C/T]TGGGCCTCTTCCCAC | 8065 |
rs557193893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011338 | GTGGAAGCTACTTTG[A/G]TTCATATTAGTTAAG | 8065 |
rs557221663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108044848 | CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG | 8065 |
rs557288967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108057847 | TTATGTAAGATGTTA[A/G]TGTTGGGAGAAGTGA | 8065 |
rs557301339 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063024 | CTAATTTTGTATTTT[C/T]AGTAGAGATGGGGTT | 8065 |
rs557319220 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108097197 | ATTTTTGTATTTTCA[A/G]TAGAGACGGGGTTTT | 8065 |
rs557321826 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023647 | AGGACTTTTCATTTA[A/T]GTGCCCCAATGCACA | 8065 |
rs557357835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108103825 | ATTTTTTTTAAATAC[A/G]TACTTTAAGTTCTGG | 8065 |
rs557371629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090009 | CGTGCCATTGCACTC[C/T]AGCCTGGGTAACAGA | 8065 |
rs557379589 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096490 | GACCCATCTCAAAAA[-/T]TTTTTTTTTTAAAAA | 8065 |
rs557395967 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099601 | TTTTTAGTTGTAATT[C/T]AGACACAATGGAATG | 8065 |
rs557414413 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065783 | CCCACCTGATTTTTG[G/T]TTCTTATGAAGGTGT | 8065 |
rs557429040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108052910 | ACAAAGTTACATCTA[C/G]TTTTTGTACTAGATA | 8065 |
rs557431975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050692 | ACTAGAAATTAAATT[A/G]CTTTTCTCCCTGTCT | 8065 |
rs557435218 | in-del | -/TA | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108090667 | AATGCTGATTATAAC[-/TA]AATTCCCATATAAAG | 8065 |
rs557440391 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108042310 | CTGCAACCTCCACCC[C/G]CGGGTTCAAGCAATT | 8065 |
rs557440897 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067785 | CTCAATCTGGTTTCA[C/T]TGCTTAAGGTGGAAG | 8065 |
rs557521222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108092087 | AGTTGTAATGAGCTG[A/T]GATTGTGCCACTGCA | 8065 |
rs557537552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011894 | ACCTCTCAAAGTGCT[A/G]GGATTATAGGCGTGA | 8065 |
rs557574908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084806 | GACTAAAATAAAAAG[A/G]ACAGATATAACACGT | 8065 |
rs557650677 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088180 | GTTAACATAAATATC[C/G]AAGAATTTAACAGTT | 8065 |
rs557682935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108077150 | GCCTAGGGCATTCTG[A/G]TATTTCATTGTTAGA | 8065 |
rs557709154 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039506 | TTTACAATTTTACCC[A/G]TTTTTAAGTGTACAA | 8065 |
rs557726126 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030464 | TGAACACAGAGAAAC[C/T]CCGTCTCTACAAAAA | 8065 |
rs557785537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108098837 | AAAAGTTCTCTAATA[C/T]TCATTTCTTCTTTTA | 8065 |
rs557844272 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086505 | TTTGATTGTTACAGT[A/G]GTTCACACCTGAGCC | 8065 |
rs557881289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090815 | GAGAGAGACCTACAG[A/G]TATTTTAACTTATAG | 8065 |
rs557903137 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108043244 | CCAACTAATTATTTT[A/G]TTTTATTTTTGTATA | 8065 |
rs557914980 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108024154 | ATTAAGAATGTGGCT[G/T]TAACAGAGCTAAACT | 8065 |
rs557970351 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108073118 | GAGGCAGGAGAATGG[C/T]GTGAACCCAGGAAGT | 8065 |
rs557974828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108030847 | TGATAAACATGCAGA[C/T]TGTGGACTAACTTCA | 8065 |
rs557985488 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058915 | AAAACAAGGTAAGAG[A/G]CTTCCGAGCTGTGCT | 8065 |
rs558001106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024863 | TTGCTAAATTCCATC[C/T]TTCCATAATCTCAAT | 8065 |
rs558034683 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108070943 | AAATACTTGTATTCT[G/T]TGTGCCAGTCTAATT | 8065 |
rs558041563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032085 | TAATCCTGGATAATG[A/G]AATAATCTGTACAAC | 8065 |
rs558192430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037828 | TCTCATTAAGGAATG[A/G]TGGGAATCCTCCCAA | 8065 |
rs558195837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064851 | GGTATTAGGGCAATA[C/T]TGGCCTCATAGAATG | 8065 |
rs558221286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108051582 | TGCTGTCATTAATGT[A/G]TCTCCTACATCTGAC | 8065 |
rs558228012 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088466 | AATCATTGACTTTAG[-/A]AAAAAAATAATTGCA | 8065 |
rs558248415 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108015385 | ATACGAAGATTTGAA[C/T]ATCATCGGTGAATGT | 8065 |
rs558253836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043949 | AATCATTTGAACCCA[A/G]GAGGCGGAGGTTGCA | 8065 |
rs558311762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108009662 | GGGAGCGGGAGATGA[A/G]TGGTCGTGCGGTGTC | 8065 |
rs558325898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084843 | AAGGATATGGAAAAA[C/T]TGGAATCATATTGTT | 8065 |
rs558351581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108078059 | GGCAAATTCTGTTTG[A/G]CCAGATATACCATTA | 8065 |
rs558356845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108103218 | TTAAGGAAATCATCA[A/G]GAAAAATTTTGATAA | 8065 |
rs558359520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108063279 | AATTTTTAGCTTCCA[C/G]AAATGAGTGAGATCG | 8065 |
rs558385308 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032162 | TACACATGTACCCCA[A/G]ACTTAAAAGTTAAAG | 8065 |
rs558390475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108077373 | TTGTGTAGGCTGGGT[A/G]TGGTGGCTTACGCCT | 8065 |
rs558395866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069338 | AAACCCCAAATCATA[C/G]ATTTTCATTCATAAT | 8065 |
rs558398247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108009963 | CTGCTTTCTAACCCC[C/T]ACCCAGTTACAGGAC | 8065 |
rs558458631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071406 | TAGCTGGGACTACAG[C/T]CGTGTACCACCATGC | 8065 |
rs558586451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084955 | AACTAATTAATCACA[A/G]CCATTTACAGATGTA | 8065 |
rs558610876 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108069811 | CTCCAGACAGGAAGA[A/G]TTAATCAAAGTTTGG | 8065 |
rs558613780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108036012 | GAGACTGTCCTAAGT[C/T]CTTTTTACCTTGTCT | 8065 |
rs558615893 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096059 | CAAGATTGCGCCACT[A/G]CACTCCAGCCCAGGC | 8065 |
rs558616864 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030569 | TTGAACCCGGGAGGC[A/G]GAGGTTGCGGTGAGC | 8065 |
rs558626434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108055927 | TGAGCCACTGCACCC[A/G]GCCACCTGGCTAATT | 8065 |
rs558632270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108028773 | AGGTTGCAGTGAGCC[A/G]AGATCGCCCCATTGT | 8065 |
rs558637109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108055140 | GAACACATTGTCCTT[G/T]GGAGCTGGTATGCAA | 8065 |
rs558639114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108062244 | TTAACATCCTTGTGT[A/G]TACATCTTTTCTCAC | 8065 |
rs558651261 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087620 | TTTTTTAATTTGTGT[A/T]TGTTTGTGTCTCAGT | 8065 |
rs558658378 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108014097 | GTGTTACCAACTGCT[C/G]TATGCTCCCTCACAG | 8065 |
rs558698194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016238 | GGTTTTTCTTTTCTC[C/T]TCTCTTCTCTTCTCG | 8065 |
rs558701724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108029377 | GAGCCAGTGAATGAG[A/C]GAATTGTAGACCTAC | 8065 |
rs558725207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108020891 | CACTACTCACTCACT[C/G]ACTCACCTAGAGCAT | 8065 |
rs558765771 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108104093 | TTGGGTAGATGTTGG[A/G]TAGAGGATGAATATG | 8065 |
rs558888002 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050747 | CCTTCTGATATCTTT[A/T]TGTTTAATTGTGGCT | 8065 |
rs558898920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095957 | AAAAATTAGCTGGGC[A/G]TGGTGGTGGGCGCCT | 8065 |
rs558902130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108057987 | AGGCCAAGGCAGGCA[A/G]ATCATGTGGTCAGGA | 8065 |
rs558914381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108079349 | GACCTCAAGTGATCC[A/G]CCCACCTCAGCCTCC | 8065 |
rs558967241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102638 | CCCTGGCTGGTTATC[A/G]TATCTATATAGGGGA | 8065 |
rs558982279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108101398 | AACTGCTGCTGTTGT[C/T]TACAGCAGATGAATT | 8065 |
rs558993962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096869 | CTGTGCCTCAGATAC[A/G]TACTTAATTTTTATA | 8065 |
rs559009990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042084 | TAATAGGACTGTGAT[G/T]GAATATAAGGGATAA | 8065 |
rs559031856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096281 | AAGAGGATTGCTTGA[A/G]CTCAGGAGTTTGAGA | 8065 |
rs559061059 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008307 | TCTTCTCTTAGTCCA[C/G]AGCTCTTACTTATTT | 8065 |
rs559072618 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009293 | CCTCCGGTCAAGGCC[C/T]GGCCGGGAGCGCCAC | 8065 |
rs559198563 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009072 | GTCAGGTCGGCTCCC[A/G]TTACCTTCTCAGCAT | 8065 |
rs559270690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108063459 | ATTTGTTGGTGGACA[C/G]TAAGGTTCCTTCCAA | 8065 |
rs559281507 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108083871 | GGTGTGGAGGAGGTG[A/T]TGTTCTAGAACAAGC | 8065 |
rs559373138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108009734 | TGTAAAGCAATGTCT[A/G]AGACGCATCAAAGGA | 8065 |
rs559376640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015751 | ATAAATGATTGAACA[A/G]TTACCATAATCTGGA | 8065 |
rs559407979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108103312 | ACACCTGTAATCCTA[A/G]CACTTTGGGAGACCA | 8065 |
rs559413589 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058878 | AGCAGATGAACAGAA[A/G]TGTATTGAATGTATT | 8065 |
rs559440356 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108022978 | TCCTGGCCCAGCGTG[G/T]TGGCTCACGCCTGTA | 8065 |
rs559458748 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108091233 | ATTTTTGTATTTTTA[C/G]TAGAGACACGGTTTT | 8065 |
rs559488549 | snp | A/G/T | 3.47695e-05 | 0.00416938 | intron-variant | CUL5 | GRCh38.p7 | 11:108088666 | AAAGAAGTGGTACAT[A/G/T]AATTTTTTGTATTTC | 8065 |
rs559541269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108074903 | GTGTGAAGTCTTAAA[C/T]TGAGTAGCCTGCAAA | 8065 |
rs559556301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108050937 | AGCTCTTCAAACTCC[A/G]TCCTCATTTTCCATA | 8065 |
rs559665728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108041079 | GGTCTCCTCTGATGG[A/G]TGACTTTGGCTCCAG | 8065 |
rs559666346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068959 | TTACATTTATCCTCT[A/G]TTTAAAACTTCCTTG | 8065 |
rs559701857 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108068881 | CAACCACCCACTCCT[A/T]ACCACCTGCCTTACT | 8065 |
rs559706363 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008421 | TATTATCTCATTGGC[C/G]AGTGGTGTGTGGTCT | 8065 |
rs559728832 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108088005 | TCAGGAAAGTGAAAT[C/G]GAGATACAAATTCTT | 8065 |
rs559732923 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105787 | ATTATTTTATATCTT[A/T]TTTGATGTTAAGTAA | 8065 |
rs559762347 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071155 | TAATTATTACTCATG[-/T]TTTTTTACCTTTTGA | 8065 |
rs559774470 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108045887 | ATAAAAAAATTTTTA[A/G]AAATAATTAAAAAGG | 8065 |
rs559776400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108019660 | TATTGTGCTGTCACT[C/G]TTATAAAAGTCTAGC | 8065 |
rs559778525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108027526 | ATCCACCCACCCCGG[A/C]CTCCCAAAGTGCTGG | 8065 |
rs559820370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108013243 | CCTCCCCTGTCCCCA[A/G]TAGAATTATTTCTCA | 8065 |
rs559839500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108026858 | GCTGGGCATGGTGGC[A/G]GGCACCTGTATTCCC | 8065 |
rs559929582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033150 | AAGTTTAGGAGAGTT[A/C]CAAATGCGAGCTTAT | 8065 |
rs559930595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108035516 | CCAAGACAGGGTGAT[C/T]GCTTGAGCCCAGGAG | 8065 |
rs559968939 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108060951 | TGCTGTGTTTTATAG[C/G/T]AGGCATTATTTTTGA | 8065 |
rs559995920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048098 | GACCCATCTTAAAAA[G/T]ATTTTTAAACGCTTA | 8065 |
rs559996381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108055226 | GGTAAGTTTTCTTTT[A/G]TTATGTTTTATGCAT | 8065 |
rs560024022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028512 | TATATTCTCAACATA[A/G]TAATGAGGGAGATTT | 8065 |
rs560074272 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019217 | GTGGGGGTGGGGTGG[A/G]GTGGATCCTGGAATC | 8065 |
rs560096557 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093388 | TCTTTTTTGTCACTC[A/C]CCACTTTTATCTTTT | 8065 |
rs560107780 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041025 | AAGTGATTTGAGTAC[A/G]GCAGGGTTACAAAGG | 8065 |
rs560109217 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042838 | TGCAGTCTTCGCTCA[C/T]TGCAACCTCCGCTTC | 8065 |
rs560111716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021372 | CCATTATTTCTTGCT[C/T]TTCCTTCAGCTTGTC | 8065 |
rs560111843 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108028899 | TTCATCTCACTTATA[A/G]TAGAAACCAAAGTCT | 8065 |
rs560159421 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007869 | CTTCAGGGTTCAAGC[G/T]ATTCTCCTGCTTCAG | 8065 |
rs560160427 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108106110 | AAACTAAAATTAATA[C/T]GTACAGTTTTCTCTA | 8065 |
rs560186594 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108099743 | TCCAGGCAGGCTCTC[C/T]GCCTACCCCAGCTGA | 8065 |
rs560216531 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020661 | GGCTAGGATTAGAGG[C/T]GTGAGCCACTGTGCC | 8065 |
rs560223194 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106764 | TCTCTTCTCTCCAGC[A/G]TACACTTAAAATTGG | 8065 |
rs560254770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066349 | ACTCTGTCTCAAAAA[A/G]AAAACCAGAGTATCA | 8065 |
rs560342831 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012992 | TTGCTGCCTTTATAA[A/T]TCTTTGCCCTTTAAC | 8065 |
rs560352242 | snp | C/T | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104923 | AAGTTAAGTATTTAA[C/T]AGTATCAAATTGTTC | 8065 |
rs560354443 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108012277 | TTTTCATTTCCAGTT[A/T]ATTGTTCCACCCCAA | 8065 |
rs560361825 | in-del | -/CT | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108049019 | ATACCATAAAATTTA[-/CT]CTCTTAAAGGATATG | 8065 |
rs560364996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108096812 | CTCAGGTAATTTGCC[C/T]GCCTCGGCCTCCCAA | 8065 |
rs560382024 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108025815 | ACCTCAGCCTTTTCA[A/G]ACTCTGAACTCTGCC | 8065 |
rs560459073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108101523 | TCCACTACATCTTCT[G/T]TGTGGCTCCTTGGCC | 8065 |
rs560467626 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108100977 | GAGGTTGCAGTGAGC[C/G]GAGATCGCGCCACTG | 8065 |
rs560518708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108094207 | CGCAAAGCAGGGACC[C/T]CTTGTAATACCGTAT | 8065 |
rs560544553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108065693 | AGGGGTAACATTGGC[A/G]ATTCAAGACTATCTT | 8065 |
rs560579642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017863 | AAAAAAAAAAGTGTT[C/T]GGAAGGTGGAGCCAC | 8065 |
rs560599741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021239 | TGGCTCTAATCCACA[A/G]TCAGTATGGCGGGAA | 8065 |
rs560600421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108074739 | TGAACCCAGGAGGTG[A/G]AGGTTGTGGTGAGCT | 8065 |
rs560601905 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108013687 | AAATCAAACTTTAAA[C/T]TGAAATATGATTCAT | 8065 |
rs560690189 | in-del | -/TTCTC | 0.0150756 | 0.0855016 | intron-variant | CUL5 | GRCh38.p7 | 11:108016237 | GGTTTTTCTTTTCTC[-/TTCTC]TTCTCTTCTCTTCTC | 8065 |
rs560735324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108086312 | CTTCAAAGTAACAAT[A/G]TAAGACTAATAGCTA | 8065 |
rs560776463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108046855 | TTTGATCAAAAATCA[A/G]AAGCTCATTTAGGCA | 8065 |
rs560789074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108014427 | GATTACAAAGGGCCT[G/T]CAGTGCTAGGCAAGG | 8065 |
rs560813272 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009247 | ACCCTGGTGCGGGCC[C/G]ACGGGCCCTGGGCCC | 8065 |
rs560848837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039680 | CCATCTATGAATTTG[C/T]TTATCTAGATAACTC | 8065 |
rs560854405 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108067992 | GGAGTGCAATGGCAC[C/G]ATCTCGGCTCACTGC | 8065 |
rs560896873 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008577 | ACGAGGGTGTTGAAC[C/T]GGCCTCAAGTGATCC | 8065 |
rs560904630 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098575 | TAAAAAAACTTTAGT[-/T]TTTTTTTTTTTTTTT | 8065 |
rs560954216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108101619 | GCCCTGTGGCAGGTC[C/G]ATTAGCTCGAAACTC | 8065 |
rs560957807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108067012 | AGTATGTACATGCTC[C/T]ACTTCTGTAGTAAGA | 8065 |
rs561001339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108094219 | ACCCCTTGTAATACC[A/G]TATTTTGTTTCTAAG | 8065 |
rs561004645 | in-del | -/AAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040611 | GTGAGACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 8065 |
rs561014238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068318 | AAAAACCTTTTTTTT[C/T]GTTTTGTTTTGTTTT | 8065 |
rs561014272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108061216 | TCCATTCAAGATGTA[C/T]TTTCAAATAACAAGT | 8065 |
rs561056930 | snp | A/T | 0.000286531 | 0.0119659 | intron-variant | CUL5 | GRCh38.p7 | 11:108095719 | TTTTTTGTTTTTAAG[A/T]CTGTATCCTCTCATG | 8065 |
rs561066485 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108048684 | TTTTTTTTTTTTTTT[C/T]GAGGTGGATTCTCAC | 8065 |
rs561070354 | in-del | -/TCTTT | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108016269 | TCTTCTCTTCTCTTC[-/TCTTT]TCTTTTCTGTTGAGA | 8065 |
rs561098044 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108060454 | ATTCCTTATACAGAG[C/G]TATATAACTAATGAA | 8065 |
rs561104220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108058066 | ATACAAAAATTAGCC[A/G]GACGTGGTGGCGTGC | 8065 |
rs561118381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100271 | CTTTAGGCTCGGCGC[A/G]GTGGCTCACACCTGT | 8065 |
rs561121707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108088729 | TTTTGCTTATAGGAC[C/T]TTCTGTGATAGTATC | 8065 |
rs561129807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102417 | CTGCAACCTCTGCCT[C/T]TCAGGCTCAAGTGAT | 8065 |
rs561161789 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108087383 | TCAATCCTTGGAAAA[A/C]AATACTTGAATTTTA | 8065 |
rs561178352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108094787 | TTGTTAATTTACTTT[A/G]TATTCCTGATATTCT | 8065 |
rs561189469 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030724 | AGGATGAACTATGTT[C/T]GTGAATATAAGCAGG | 8065 |
rs561213013 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108049333 | GGGGTTTTTTGGTTT[A/C]TTTTTTCATTTGTTT | 8065 |
rs561288616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108053406 | GTATTTATTGAGTTA[A/G]TGAACCTATAGAGTT | 8065 |
rs561305208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108019575 | CTGGCAATGTTTATT[G/T]TAGCCCTTGTAACGT | 8065 |
rs561316936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038242 | TTGTTTTTGCCAGTC[A/T]GTGTTGATAAGATTT | 8065 |
rs561348874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059915 | TGAATAATACCCTTT[A/T]GTATTAGCAGAATTA | 8065 |
rs561390923 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082635 | TGTATAAAAACACAA[C/G]TGATTTTTTTTTCTG | 8065 |
rs561417546 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108034035 | AGTATTACTAGTTAC[A/G]TTGAGGGTCTCCAAG | 8065 |
rs561431435 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108040231 | ATGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG | 8065 |
rs561452553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038662 | CCTGGGAAACAAGAG[C/T]AAAACTCCATCTCAG | 8065 |
rs561508010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023859 | CCTAAAAGTTTAAAC[A/G]GAGTGTGGTATGAAA | 8065 |
rs561508039 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066557 | CCAAAATCTTGCAAG[A/G]ATTCTTTTAACTCAC | 8065 |
rs561531431 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089347 | AGGACTGGGTATTTC[G/T]CAGAGATGGATAATT | 8065 |
rs561537372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108080552 | AGGTGTGTGCCACCA[C/T]GCCCAGCTAATTTTT | 8065 |
rs561571406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108071615 | GCAATGGTGCAATCA[C/T]GGCTCACTGCAGCCT | 8065 |
rs561596110 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063980 | TCATCTGCAAACAAG[C/T]GTAGTTTGACATCTT | 8065 |
rs561627039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033172 | CGAGCTTATCTTGCC[C/T]TCTCCCCATGTGGTC | 8065 |
rs561696099 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108066468 | ACTCCAATAAGAAAT[A/T]TTTTTTTATTCATAC | 8065 |
rs561722391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085673 | TGAAAACTTGATGCT[A/G]AGTAAAAGAAGTGGG | 8065 |
rs561760754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032122 | CCATGACACAAGTTT[A/G]CCTTTGTAACAAACC | 8065 |
rs561783455 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108078589 | TTTAAATGTAAATTT[G/T]CCTATTACCGTTTTA | 8065 |
rs561787988 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092132 | ACAGAGTGAGACCCT[G/T]TCTCAAAAACAAAAA | 8065 |
rs561810390 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108031565 | AGTCCTTTCTCTTTT[A/G]CTTTTGTCAGGTTTG | 8065 |
rs561994173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017085 | AGCATTTATGCTGTA[C/T]TGGATACCATTTTAA | 8065 |
rs562024827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108044424 | GGAGGCTGAGGCAGG[A/G]TTGAGCCCAGGAGGT | 8065 |
rs562030363 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076815 | GTAGAATGTGATAGA[A/G]ACTAGTCAGGGATGA | 8065 |
rs562049057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108070267 | CTTACTAAGTTGCTC[C/T]TAGTTAATTCTTTTC | 8065 |
rs562064075 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030949 | TTCACGTAGGTTGTT[G/T]TCAGATCATATGTTG | 8065 |
rs562137717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108076913 | ATAGTTTTTGGAGAG[A/G]TGGTTGCAGAGAGAT | 8065 |
rs562141250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030529 | TTAATCCCAGTTACT[C/G]GGGAAGCTGAGGCAG | 8065 |
rs562188753 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108021053 | GCCTCCAGCTTCAGT[A/G]CAGTTACATGCTATA | 8065 |
rs562194972 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023886 | GAAATTTTTTATTTC[A/G]GTGGAAAGAGATATT | 8065 |
rs562209702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071055 | GAAGGTCAATAAAAT[A/G]GCATAACATGAAAAA | 8065 |
rs562211708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064357 | TTGAACCATCCTTGC[A/G]TCCACGGATAAATCC | 8065 |
rs562218446 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108011494 | TTAACTTGAACATTT[A/T]CAAATAAAGGGAAGG | 8065 |
rs562222807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108052349 | AGACAGGGTCTTACT[C/G]TGTCACCCAGGCTGG | 8065 |
rs562248046 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038981 | GAGATTGTTCTGCAT[A/G]TTGTGCAATATTTAT | 8065 |
rs562249893 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105915 | GGATCTGTCCCCATC[C/T]GAAGAGGCTTTGTGA | 8065 |
rs562262469 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070332 | ATACTTAAGGAAATA[G/T]ATAAAATATTTAACA | 8065 |
rs562263058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108058783 | TTTTATTTTTACTTA[C/T]AGGAGAGCCACTTAG | 8065 |
rs562278627 | snp | A/G | | | synonymous-codon | CUL5 | GRCh38.p7 | 11:108089614 | AGAAAACATGGTAGA[A/G]TGGCTAAGAGTAAGT | 8065 |
rs562286487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059251 | CATACCTTAGTATTT[C/T]CTGGGGAAATTCAAT | 8065 |
rs562289198 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066340 | CAGAGCGAGACTCTG[C/T]CTCAAAAAAAAAACC | 8065 |
rs562295223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010727 | TAAGAAAACTAATTC[G/T]GGGAATTGAGTAACC | 8065 |
rs562311242 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041166 | AGCTTCCTTTCTTGT[C/T]TCCTCTACAGGGATC | 8065 |
rs562332125 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072650 | TTACCCATTAGGGCG[A/G]ATATAGCAAGTAACA | 8065 |
rs562341448 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108091626 | CCTGTGAGGTGGAGG[G/T]TGCATTGAACAGAGA | 8065 |
rs562382185 | snp | A/C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017588 | GATGCGGAGGCTCAC[A/C/G]CCTGTAATTGCAGCA | 8065 |
rs562387966 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108049454 | TCAAGCAATCCTCCC[A/C]CCTCAACCTCCTAAG | 8065 |
rs562427715 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108053985 | AGAATAGCTGAGATT[A/G]CAGGTGTGTGCCATC | 8065 |
rs562446560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108051857 | TAGTTAATTTTTACA[A/T]CCACTGAAATTTGCA | 8065 |
rs562479801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108086226 | CCTAGGTACATCATA[C/G]TAAAACAGCTTACAA | 8065 |
rs562509003 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108067109 | GTGCAACATTTGGAA[G/T]TTATGTGGCTACTCT | 8065 |
rs562543416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108073062 | AAAAAAATAGCCAGG[C/T]GGGGTGGCGGGCGCC | 8065 |
rs562642897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108072590 | AGGTTGGTTAGTGGG[A/G]TATAAAGTTATAGTT | 8065 |
rs562703408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071565 | TTTTTATTTTTATTT[C/T]TTGAGACCGTCTTGC | 8065 |
rs562704695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066599 | ATTGTAATAAAGTAG[C/G]TCAGATCATCTAGCC | 8065 |
rs562733133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018938 | TCTGTGCCTCAGTTT[C/G]TATATCTATAAATAG | 8065 |
rs562748097 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024083 | AAGGGCTGGATCTGG[C/T]CCATGGATTAGAAGC | 8065 |
rs562783762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011634 | TTCTTTTTAATTTTT[A/T]TTTTTTTGGAGGGGG | 8065 |
rs562834860 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039488 | ACTGCTGCTCTAGAT[C/T]CATTTACAATTTTAC | 8065 |
rs562839344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038840 | TTAGGTTGCTTATAT[C/T]TTTCTAAATCTTAGT | 8065 |
rs562859502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108025165 | TTAAAAAATATTTCT[A/G]TGATGTTCATGCCAT | 8065 |
rs562869159 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103015 | TGCCCAGGCTGTTCT[C/T]AAACTCCTGGACTCA | 8065 |
rs562929835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099724 | CCAGTCATCTTCCCA[C/T]GTTTCCAGGCAGGCT | 8065 |
rs562932227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024517 | AAGTGTTTGGAACAG[C/T]ACAGCACCTAACATG | 8065 |
rs562957415 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108059299 | CCACAGTGTGTCAGG[C/T]ATTATGCTAGTTGGG | 8065 |
rs562957890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108057521 | AATATTATTTCTGTT[C/T]TACTCTTGCCAAAAA | 8065 |
rs562965097 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052633 | AATAATTGAAAATTA[C/T]GTTACAATTTGTTCT | 8065 |
rs562968702 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081024 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 8065 |
rs562975110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108041799 | GTTTCATCATGTTGG[C/G]CAGGCTGGTCTCGAA | 8065 |
rs562991620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108093190 | AAAGAGTAGTTTGAA[C/T]AGCTTTTGCCTTCTT | 8065 |
rs563000816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108091005 | TAGCAAAACTAATAC[A/G]TATTTACTACGAGAA | 8065 |
rs563038679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108045922 | AATAGTATACATCTA[A/T]TGTGTTAAAGAATTA | 8065 |
rs563050624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108053155 | TGAAAAGGAGAGCAT[A/G]TAGGAGTACATTCTC | 8065 |
rs563072307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108052541 | TGTTGGGACTACAGG[C/T]GTGAGCCACTGCACC | 8065 |
rs563086049 | snp | A/G | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108092608 | CCCAAAGACCATATC[A/G]TATGATTCCACTAAT | 8065 |
rs563088959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050513 | CTGGGACTACAGGCA[C/T]GTGCTACCACACCCG | 8065 |
rs563128583 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035995 | AAGTCCGAGTGATCA[G/T]CGAGACTGTCCTAAG | 8065 |
rs563167744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096961 | GACTTGTAGATTGTA[C/T]TCATTAGCCCCCTGC | 8065 |
rs563206428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108045181 | GTTCTGAGTTTTTGT[A/G]TATCAATTTATGATA | 8065 |
rs563288102 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108097422 | AGTTTCTTGTCTTAC[C/T]GTAAAGAGAGCATTT | 8065 |
rs563305479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042305 | GCTCACTGCAACCTC[C/T]ACCCCCGGGTTCAAG | 8065 |
rs563312817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016392 | CCCACCTCATCCTCC[C/T]ACAGGTGCAACACCA | 8065 |
rs563314127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108076984 | TTAAACATCCATATG[A/G]TAATGTTGAGTCTGG | 8065 |
rs563373841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043547 | AGATCACTTTAGCTT[C/G]TTGTTTAATAGATTG | 8065 |
rs563379124 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030863 | TGTGGACTAACTTCA[A/G]GAGATTCCGATCCAG | 8065 |
rs563395929 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012393 | TTAACTTCCTTGGTC[A/G]ATACCAAACATTTTT | 8065 |
rs563430431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108036275 | TTTATTCTGCTCCCA[A/G]TACTCAGAGAGTTTA | 8065 |
rs563438087 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037467 | TACCATGTAGTTGTA[A/T]TCATGGCTATGAATT | 8065 |
rs563511401 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036490 | TTAAATTTATTTATT[C/T]ATTATTGAGACAGAG | 8065 |
rs563541887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108068995 | AGGCCTGATGGTTCA[C/T]ACCTGTAATCCCACA | 8065 |
rs563577155 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038042 | CCGAAATGATGTAGG[A/T]CCTTGCTGCATACTA | 8065 |
rs563638887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108077735 | AGATCACCTGAGGTG[A/G]GGAGTTTGAGACCAG | 8065 |
rs563649958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108082739 | AGCCTTCGCCTCCTG[A/G]GCTCAAGCCTCCACC | 8065 |
rs563690472 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108089290 | GACCGACTAACAATT[G/T]GGTTATAGTCTCAGT | 8065 |
rs563740957 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108038566 | AGTAATTCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 8065 |
rs563772906 | in-del | -/TTCTTGTGTGA | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108084579 | GATAACATCATCTTG[-/TTCTTGTGTGA]TTCTTATATATACAG | 8065 |
rs563794220 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060482 | GAAAATCAGAAATGC[-/T]TTTTTTTTTAAACGA | 8065 |
rs563813637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108083536 | TGGCTCATGCCTGTC[A/G]TCTCAGCACTTTGGT | 8065 |
rs563897312 | snp | A/G | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104819 | TTTTTAAAAAATGCA[A/G]TTAAAACTAGAAATA | 8065 |
rs563918178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108078436 | AAATTGACTTTATTT[C/T]TTCAGGTAAAAAAAA | 8065 |
rs563932061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010607 | CTGTATCATAGGAAC[A/G]TTGTGAAGATTAAAT | 8065 |
rs563954879 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058537 | ACAGACGTGAGCCAC[C/T]GCACCCGGCCCAAAG | 8065 |
rs564010810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090535 | AGGACAAATTATTAT[A/G]TCTTTAAGGTATTTT | 8065 |
rs564026536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023029 | CAAGGCAGGTGGATC[A/T]CCTGAGGTCAGGAGT | 8065 |
rs564046492 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016493 | TCCTGGGCTCAAGCA[A/G]TCTGCCCTGTCCTTC | 8065 |
rs564082106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108071594 | GCCCTGTCACCCAGG[C/T]TGAGTGCAATGGTGC | 8065 |
rs564105254 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108098070 | TTCGTTTTTGTTTTT[G/T]TTTTTGTTTTTGTTT | 8065 |
rs564142747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085590 | TAAATCTTTTTTACT[C/G]TTAGTAAAAGATATG | 8065 |
rs564146815 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019761 | GTGACTGTGTTACTG[A/G]TTTATGTATATCTTA | 8065 |
rs564163267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108038600 | TAATCACTTGAATCC[A/G]GCAGGCAGAGGTTGC | 8065 |
rs564166599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085230 | TGTATCCATACAGTG[A/G]AATATTATTCAGTTC | 8065 |
rs564199942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030440 | GTCGGGAGTTTGAGA[C/G]CAGCCTGATGAACAC | 8065 |
rs564215517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108044208 | AAAACTTTGGGCTCT[A/G]CTAGTGTCTCTAAAA | 8065 |
rs564228523 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042972 | TTCGCTATGTTGGCC[A/C]GGTTGGTTGCGAACT | 8065 |
rs564260572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108029833 | CAGAGCCTAACCAGT[A/G]TTTAATTTATCTCCA | 8065 |
rs564285623 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020291 | CCAGAAGAAGGCGTT[G/T]TTACCATAGGAGATG | 8065 |
rs564310816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031165 | ATGAATCCAGGAGTT[C/T]GAGACCAGCCTGGGC | 8065 |
rs564396822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024550 | ACAGTCAGATATTAT[A/T]AAGTAAAATAATCAC | 8065 |
rs564423495 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108051073 | CACTCAGGCATTACA[A/C/G]TAGTGTAACCTGGGC | 8065 |
rs564423559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108058618 | GTGGTGGTAATGCTT[C/T]TCCTGCTGCTTTTAC | 8065 |
rs564485475 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108058317 | GCAGTAGTGCAGTCT[C/G]CGCTCACTGCAACCT | 8065 |
rs564488877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108083643 | AAATGTTTTAAAAAT[C/T]AGACGAGCATGATGG | 8065 |
rs564523879 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108048133 | ATTTTTTTTTTTTTT[C/T]CATGAATCATTTTAC | 8065 |
rs564526400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031766 | AAAGACGTGAAATCA[C/T]CCCCAATGCCCATCA | 8065 |
rs564541844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108036468 | TCTTTCAACCCCCCA[A/C]TTTACTTTAAATTTA | 8065 |
rs564577464 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020446 | TTAATGAAAAAGATT[A/G]AGAATAAAAAACCTT | 8065 |
rs564608268 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008743 | AAGACAGCTGTTGTA[A/G]GCATTTCAGGACAAT | 8065 |
rs564613950 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108076875 | AGGATATGTTCACTG[C/T]GATAGGGAAGACTGT | 8065 |
rs564647946 | in-del | -/T/TT | 0.00450254 | 0.0472429 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033786 | AAACTCCCTTTTATC[-/T/TT]TTTTTTTTTTTCAAG | 8065 |
rs564649947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108101918 | CTGAACCCCTGACAT[A/G]AACCCCAATTTATGA | 8065 |
rs564684203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016416 | AACACCAGCATTCCC[A/G]GCTCATTTAAAAAAA | 8065 |
rs564706475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108070004 | CAGTATAATTTTTTT[G/T]TTGTTGAACAATATT | 8065 |
rs564742247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108097529 | ACCACACATTTTAAG[G/T]TTGTGTTTGTAATCT | 8065 |
rs564744141 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105081 | GAGTTTTTTTTTTTT[A/T]AAATATGGCTGGAAA | 8065 |
rs564747947 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108049290 | TATGGCTGAATAATA[G/T]CTATTGTTTGGATAT | 8065 |
rs564767219 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108068868 | CGTTACCATATCCCA[A/G]CCACCCACTCCTTAC | 8065 |
rs564771569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108010142 | GAAGAATGAGGAAGA[C/T]TTAGAACTAGTCTGT | 8065 |
rs564774449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021277 | AATCTTAAAACAACT[A/G]AACTGGTTGTGTGGT | 8065 |
rs564781342 | snp | C/T | 1.7058e-05 | 0.0029204 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104394 | GCATAATTTTGAATA[C/T]CATGGACAATATTTA | 8065 |
rs564782103 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009257 | GGGCCGACGGGCCCT[A/G]GGCCCTGGTGGGAGC | 8065 |
rs564836424 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108035758 | ACCTTGTCTCAAAAA[A/G]AAAAAAAAATTGAGG | 8065 |
rs564880796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108022017 | ATCTATCCATCGATC[C/T]ATCCATTCTTAGAGA | 8065 |
rs564908875 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108054518 | AAGGATTTTGTCTTA[C/T]ATAATTATATGTTCT | 8065 |
rs564916616 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101784 | AGGTTCTCTAACTAC[C/T]ACCTTCACCTCTATC | 8065 |
rs564920102 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079782 | CATCTGCTGTCCTGA[G/T]TAATTCCCTCAATAT | 8065 |
rs564922517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108089335 | AAGTAGTGTATCAGG[A/G]CTGGGTATTTCTCAG | 8065 |
rs564959398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096145 | CACGAGATATTTATG[C/G]AAAAAATAAATTGCA | 8065 |
rs564969551 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086648 | AATCCATTTCTAAAT[G/T]TTCAACTTCCACATT | 8065 |
rs564982348 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108046949 | TTTCAAATCAGCCAC[A/C/G]GCCTCTCTTATGAAT | 8065 |
rs564989253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087921 | AGTGAGCCAAGATGG[A/C]ATCATTGCACTCCAG | 8065 |
rs565019695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108062764 | TATTATTTTTAAACA[C/T]AAAATTAAATTATTT | 8065 |
rs565045218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042323 | CCCCGGGTTCAAGCA[A/G]TTCTCATGCCTCAGC | 8065 |
rs565080617 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108096827 | CGCCTCGGCCTCCCA[A/G]AATGCTGGGATTACA | 8065 |
rs565123064 | snp | C/G/T | 4.98081e-05 | 0.00499019 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094849 | TCTGAATGCTGGCGC[C/G/T]TGGTCAAGAAGTTCT | 8065 |
rs565126668 | snp | A/T | | | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074516 | TGTCTATTTTAAAAC[A/T]AGTAAATAGGCCAGG | 8065 |
rs565139754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090217 | ACAGGGGCTGGGCAC[A/G]GTGGCTCACACCTAT | 8065 |
rs565154830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108081368 | AGTTAGCTTTTGTAT[A/G]TGGTGTGAGATACAG | 8065 |
rs565187603 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108050230 | ATTCTTTTTTGTCTT[A/T]AGCTTCAATCTTCTT | 8065 |
rs565247250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108047907 | CTTGGATGTTCTTAA[C/T]AGATGTTAAAAAATA | 8065 |
rs565255045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108047050 | GGACAGGGCACAGTA[C/G]CTCAGGCCTGTAATC | 8065 |
rs565255189 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032854 | ATGAGTATTTTTCTG[-/T]TTTTTTTTTTCTCCT | 8065 |
rs565258624 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007797 | TGAGACAAGAGTCTC[G/T]CTCTGTCGTCCAGGC | 8065 |
rs565322203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013506 | TCTCTCTCATACATG[A/T]GTGCGTACACACTCC | 8065 |
rs565382849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095818 | AGAAAAATAGAGGCC[A/G]GGCACAGTGGATCAC | 8065 |
rs565488471 | snp | C/T | 8.4369e-05 | 0.00649441 | intron-variant | CUL5 | GRCh38.p7 | 11:108088499 | CATTAATCATTTTTC[C/T]ATCAACTGCTTTTAA | 8065 |
rs565514105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034185 | ACATGGGGTGAAGTG[C/T]AGGAAAAAACAAGCA | 8065 |
rs565537936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028368 | TAGGAAGTCCTGTTA[A/G]TACCACCTTTTGGGC | 8065 |
rs565598006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108027710 | TTGCGCCTGGCTCCT[C/T]GTTTCTCTTAATTCC | 8065 |
rs565599916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034903 | GGATGAAATCCTGAA[C/T]TTTTAAAACTTTTCA | 8065 |
rs565611783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108082379 | TTGCCCTCCTGAGCT[C/T]GAGTAATCCTCCCAC | 8065 |
rs565671404 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108058119 | GAGGCTGAGGCAGGA[G/T]AATCTCTTGAACCTG | 8065 |
rs565675400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108081620 | AGCCAGGCGTGGTGG[C/T]GGGCACCTGTAGTCC | 8065 |
rs565683381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108074056 | TAGTGTAATAAACCT[A/G]TAACAAGAAATTGCT | 8065 |
rs565687906 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056163 | ACTGACCTTAGGGTG[C/T]TTCAGTATAAGGAAA | 8065 |
rs565718049 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008827 | AGGTCCCGCCAGCAG[A/C]GGGCACGGTCCCGGC | 8065 |
rs565735742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108073584 | TTGCATTATTTTTCT[A/G]TTAATTATAAACTTA | 8065 |
rs565740128 | snp | A/T | 4.18576e-05 | 0.00457461 | intron-variant | CUL5 | GRCh38.p7 | 11:108089639 | GTAAGTAAATTTTTT[A/T]AAATATTTGGTTTTC | 8065 |
rs565761000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042341 | CTCATGCCTCAGCCT[C/T]CCAAATTGCTGGGAC | 8065 |
rs565797153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074322 | GCCTCAGCCTCTCGA[A/G]TAGCTGGGATTACAG | 8065 |
rs565852269 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086991 | TTTTTTCATTCCTCA[C/T]CTAACTGGTAGATGT | 8065 |
rs565867909 | snp | C/T | | | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108107975 | ATGTAGCTTTTCCAC[C/T]GATGATAGCATGTGG | 8065 |
rs565885726 | snp | G/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106432 | TGGGTAACACTACAT[G/T]CATAGCAAAGTTTTT | 8065 |
rs565902606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033479 | CAATCCAGTATGACC[C/T]AAGGCCTCCCAAAGA | 8065 |
rs565939842 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108069232 | TATGTAGTAATGCCA[C/G]TGTACTCCAGCTTGG | 8065 |
rs565956749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108068054 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 8065 |
rs565967464 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108029257 | CTGTTGGCTTCCCCA[C/T]GGCCCATTTGTGTGA | 8065 |
rs565981987 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083893 | AGAACAAGCTTGTCC[A/C]ACCCTGCGGGCTGCA | 8065 |
rs566016742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095265 | TAGCTTACACCTTTC[A/G]TTAGGGACAACTTCT | 8065 |
rs566064433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108081491 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 8065 |
rs566071617 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087794 | ACATGGCAAAACCCC[A/G]TCTGTGCTAAAAATT | 8065 |
rs566115114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108041922 | AAGGCTTCTTAAACT[A/G]ACACCAGTCAATGTG | 8065 |
rs566125103 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034105 | GACTGAACATACAAT[C/T]ATACTCACAGCTTTG | 8065 |
rs566165550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108026186 | TCTGCTTGGGAAAAG[C/T]GTACAACCCTGGTTA | 8065 |
rs566166684 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098187 | ACTTTGTTTTTACAG[A/C]GAATGTAGTCACTTG | 8065 |
rs566255786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108019016 | ATGTACAGACCTTTT[C/T]TTCTTATAATTCCCT | 8065 |
rs566267355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013972 | ATATGCAAGGTACCA[C/T]GGAGAATGCAAAGAT | 8065 |
rs566273598 | snp | A/G | 1.6628e-05 | 0.00288335 | intron-variant | CUL5 | GRCh38.p7 | 11:108054837 | TTGAGCAATTCCCTT[A/G]ATATTCTTAAAATGA | 8065 |
rs566286329 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108054093 | TCAAGTAATCTGCCC[A/G]CCTTGGCCTCCCGCA | 8065 |
rs566321058 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014746 | GAACTAGGCAGACAG[C/G]TCCTGCCCTTGTATA | 8065 |
rs566321859 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108037215 | GGAATGAGGTAGCCA[A/G]TTTTCCTGGTTTAGA | 8065 |
rs566324289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108014718 | TATTTCCTAATTCTA[A/T]CTAGATAATGATGAA | 8065 |
rs566333773 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064642 | TTGAACTTGGGAGGT[A/G]GAGCTTGCAGTGAGC | 8065 |
rs566347494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108053604 | TGTTTAACCCATATG[A/G]TGTTCATAAGATTAA | 8065 |
rs566394586 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040016 | TCTTCTACACAAGGA[A/T]ATCAAAACCTCTGGA | 8065 |
rs566400557 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066852 | TTTTCATACACATCT[A/G]TACATATGAACCATA | 8065 |
rs566407094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012514 | GACTTGGTGGTATGT[C/T]CCCTCTTACTTTTTT | 8065 |
rs566455034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059664 | TGGGTGGATCATGAG[A/G]TCAGGAGTTCAAGAC | 8065 |
rs566464341 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106987 | TTGCCATCTCGTTGC[C/T]GGAGTAAGTAGACAT | 8065 |
rs566472287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108047259 | AAGATTGAGGCTGCC[A/G]TGAGCCGTGATCATG | 8065 |
rs566492759 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108072684 | TAGTGTATATTTCAA[A/G]ATAGAAGAGATTTTT | 8065 |
rs566499218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018453 | AGGCGGATCATGTGA[C/G]GTCAGGAGTTCAAGA | 8065 |
rs566625123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087525 | GCTGGGTGCAGTGGC[A/C]TGCACCTGTAGTCCC | 8065 |
rs566729093 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108011839 | CACCATGTTGGCTAG[A/G]ATGGTCTCCATCTCT | 8065 |
rs566745126 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108100326 | GGTGGGCAGATTGCC[C/T]GAGGTCAGGAGTTCA | 8065 |
rs566766101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108086751 | ACCCATTCCCAGTTT[A/G]CAAAGAAAGGCATAC | 8065 |
rs566779114 | snp | C/G | 1.69401e-05 | 0.00291029 | missense | CUL5 | GRCh38.p7 | 11:108094457 | GACATAAAAGTATCT[C/G]AAGATTTGAACCAAG | 8065 |
rs566821519 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036398 | AGCAGCATATTACAT[A/G]TTATGTCAGTTTTGA | 8065 |
rs566821729 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108025692 | ATGGTTCTTTCCCCA[G/T]TCTCTTACAGTTTTC | 8065 |
rs566827141 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108092760 | GATAGTGGTGATGGT[A/T]GCACAGTTCTGTAGA | 8065 |
rs566828163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108052115 | GGACTACAGGCACAT[A/G]CCAGCATGCCTAGCA | 8065 |
rs566877245 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108044139 | CACTGGACCAGATAC[C/T]ATTATCAAGCTGAAT | 8065 |
rs566889578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108051631 | GATATAATCACCAAT[A/G]TTTATATACCATTTT | 8065 |
rs566938194 | in-del | -/TCTAT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047589 | ATGGAGTAAGACTAA[-/TCTAT]TGGATATTACTTAAG | 8065 |
rs566951895 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108012587 | AAAGTTCATATGTCG[C/T]GTCATATAAACTTTT | 8065 |
rs566963178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108091801 | ATAGACAGATGGCCA[A/G]TAAGTGCATGCAAAG | 8065 |
rs566982513 | in-del | -/A | 0.00358779 | 0.0422022 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007110 | ATTTTATTATTTTTT[-/A]ATAGCGATAGCTACT | 8065 |
rs566985510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085861 | GGTAATGAAAGTGTT[C/T]TAAAATTTTATTATG | 8065 |
rs567036805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013059 | GTATAGAACCTGTCA[G/T]TCATAAAAGTATTAG | 8065 |
rs567061458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031774 | GAAATCACCCCCAAT[A/G]CCCATCAATGATAGA | 8065 |
rs567074105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108040438 | TCAACATGGTAAAAC[A/C]CTGTCTTTACTAAAA | 8065 |
rs567080208 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081380 | TATATGGTGTGAGAT[A/G]CAGCTCTAACTTCAT | 8065 |
rs567127926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071957 | CAAGGCGAGAGGATT[G/T]TGTGAGCCCCGAAGT | 8065 |
rs567143022 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102324 | TGAGCCACCATGCCC[A/G]GCCTATTTTTCTATT | 8065 |
rs567191156 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108108087 | TGTCATAACAAAATT[A/C]AAATTTTATAGCAGA | 8065 |
rs567199887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108034284 | TGACAGCGTGTGATA[C/T]GTTGTCTACCAGAGA | 8065 |
rs567209570 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007510 | ATGGCAGATAACAGG[C/T]GGGGTCAATGGAATG | 8065 |
rs567271628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108060219 | TTAAGCTTGGTGTTC[A/G]AAAAGACAAGGTGAT | 8065 |
rs567274946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108054165 | TTTTTCTGTAGACAC[A/G]TGATTTTACTATGTT | 8065 |
rs567279013 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108106075 | TGTCAATTATTAGAC[C/T]GAGCATATTGTGAAG | 8065 |
rs567312292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108093498 | CTCCATTTATGTTCT[A/G]TTTTATTTTCATTTC | 8065 |
rs567321614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108101024 | CAGAGCAAGACTCCA[C/T]CTAAAAAAAAAGAGT | 8065 |
rs567336898 | snp | A/T | 8.80863e-05 | 0.00663592 | intron-variant | CUL5 | GRCh38.p7 | 11:108094553 | TATATTTTTTAAACT[A/T]AGAAGAATATCTTTG | 8065 |
rs567351432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108092859 | TCTCACTTTGTTGCC[C/T]AGGCTGGAGTGCAGT | 8065 |
rs567376113 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108086583 | ATGGCTACCTAAGGG[A/G]ATACAGAAAGACTTC | 8065 |
rs567442465 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108081054 | CACTTTGGGAGGCCA[A/G]AGCGGGTGGATCACT | 8065 |
rs567461426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108088069 | TTTTAATGCATGATG[G/T]TATATATATCATCAT | 8065 |
rs567468310 | snp | A/G | 5.00789e-05 | 0.00500369 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054705 | GGACAATTTTGAGAA[A/G]GCATACTTGGATTCA | 8065 |
rs567500493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095047 | AAAGTAGCAGGACTC[C/T]GCAGAATTGCTTAAA | 8065 |
rs567500545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087614 | AAAAAATTTTTTAAT[A/T]TGTGTATGTTTGTGT | 8065 |
rs567507933 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108024676 | ATTCAAACCATTCGT[-/G]GAAATGTAAGGAAAA | 8065 |
rs567566270 | snp | A/G | 0.000364456 | 0.0134943 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108052710 | AAACATAAAAAACAG[A/G]CTCCAAGATAGTGCA | 8065 |
rs567570092 | in-del | -/T | 0.0295035 | 0.117819 | intron-variant | CUL5 | GRCh38.p7 | 11:108071871 | TCACTTTTAATTCGA[-/T]TTTTTTTTTAAACAT | 8065 |
rs567614683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108045395 | ATTTGAGTTCAAGCC[C/T]AGACTGGGCAACATA | 8065 |
rs567704650 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108079292 | TGTATTTTTAATGGA[A/G]ACGGGGTTTCGCCAT | 8065 |
rs567717222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108070544 | TGGAACCTTGTGATG[A/T]ATCTTTTTAGAATGT | 8065 |
rs567726657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032418 | GAGGATCAGGCAGGA[C/G]AATTGCTTGAGCCCA | 8065 |
rs567729419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108031868 | GATCATGTCCTTTGC[A/G]GGGACATGGATGGAG | 8065 |
rs567751194 | in-del | -/AAG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108078564 | CCATAATGTTATAAA[-/AAG]AACTCAGTTTAAATG | 8065 |
rs567778552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064614 | ACTCGGGAGGCTAAG[A/G]CAGGAGAGTTGCTTG | 8065 |
rs567798805 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108039095 | GCGCAATCTCGGCTC[A/T]CTGCAACCTCTGCCT | 8065 |
rs567868799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108026420 | CTTCTCAGACATTGT[C/T]GTTATTTCCACATCA | 8065 |
rs567937592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108065171 | GCTGGGACTACAGGC[A/G]CCCGCCACCACACCC | 8065 |
rs567951286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059186 | CCCAGCTTTAAGCCA[A/C]AATGACTTAAAATTT | 8065 |
rs567982386 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108091934 | ATGAAGCCAGGAGTT[A/T]GAAACTACCCTGGGC | 8065 |
rs567985994 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | CUL5 | GRCh38.p7 | 11:108028628 | CGGATCACAAGGTCA[C/T]GAGTTAGAGACCAGC | 8065 |
rs568011604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030707 | ACAGTATATTAACTT[C/T]TAGGATGAACTATGT | 8065 |
rs568064210 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034498 | CAAAGGCTAATCTTA[A/C]AAGCAGGCATTTCTA | 8065 |
rs568064628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108031199 | ATGGCGAAACCCCGT[C/T]TCTACTGAAAATACA | 8065 |
rs568084038 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108077110 | TAATGATTGGAGATA[C/G]AAAAGAGGACAGATC | 8065 |
rs568142327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015516 | ATTGCCCTCTTGAAA[C/T]GTATATCTAAGAGGG | 8065 |
rs568144335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108023222 | CCATTGCACTCCAGC[C/G]TGGGCAACAAACAAA | 8065 |
rs568181690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108053310 | CTGTGCCTCCTTGGC[A/G]TAGTACTTTTGTTTA | 8065 |
rs568232662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099323 | TGTACTTTTTAAAAT[A/G]TAAAACAAGACGAAA | 8065 |
rs568234153 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108058994 | AGCAAGAAAAAAAAT[G/T]AAGCCAAATGCCTTT | 8065 |
rs568266104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043117 | TTACTCTGTCGCTCA[C/G]GCTGGAGTGCAGTGG | 8065 |
rs568269400 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, missense | CUL5 | GRCh38.p7 | 11:108106222 | ATAATTCAGCATTGG[C/T]GTATTTGCTTGTCCC | 8065 |
rs568290052 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017535 | TACTGGTAATTAGGG[C/G/T]GGTAGCGAAAACAAC | 8065 |
rs568291699 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083530 | GTGCCATGGCTCATG[C/T]CTGTCATCTCAGCAC | 8065 |
rs568357769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011301 | GAAGCTATTTTGGTT[C/T]ATATTAGTTAAGTAC | 8065 |
rs568379434 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108018199 | CTGCATTCTAAGGCA[A/G]AGGTCTTGAGGTGCA | 8065 |
rs568386086 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108063141 | TGAGCCACTGCACCC[A/G]ACTATTCATTCTGGT | 8065 |
rs568456950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043693 | AAAATAAGGATAAAA[C/T]AGTAGTACTTTAGAA | 8065 |
rs568475695 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108009552 | GGCCTTGGGGTCGAC[A/G]GGCTCTGGTGGTCGC | 8065 |
rs568531151 | in-del | -/TG | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108035111 | TCTGTTGTTGCAAAC[-/TG]TAACCAATCCAGAAA | 8065 |
rs568545725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108103587 | AACTGAATACAAGGG[A/G]AAAATTTGGTGTAAG | 8065 |
rs568547112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031749 | GCACTGTTCACTCTA[A/C]CAAAGACGTGAAATC | 8065 |
rs568550874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108084082 | TGGCCCAGGGAAGCC[A/G]AAAGATTGGACACCC | 8065 |
rs568594176 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108094100 | CAGTTAAATTTATTA[C/T]ATAGTGTCAACTGAA | 8065 |
rs568650487 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011114 | GAAGTAATTTTGTCC[A/G]TGATTCTGGAAAATT | 8065 |
rs568697067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108036991 | AAGCTTTGCTCCAGC[C/T]CTGGGCTCTGATCTT | 8065 |
rs568733175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059633 | CCTGCAATCCCAGCA[C/G]TTAGGGAGGCCGAGA | 8065 |
rs568772527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064690 | ATTGCAGCCTGGGCA[A/G]CAGAGTGATACTCTG | 8065 |
rs568778789 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108091116 | GATTGCAGTGGTGCA[A/G]TCTTGACTCACTGAA | 8065 |
rs568816690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018324 | ATACAATCAGCCCTC[A/G]GTATTCATGAGTTCC | 8065 |
rs568850845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108071351 | CTGTAGCCTTGACCT[C/T]CTGGGCTCAAGCGAT | 8065 |
rs568888913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108078692 | AATCTGAGCTAGTTA[C/T]AGCACTTTCAGAGTA | 8065 |
rs568941281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108009924 | AATTCTCCCATTCTT[A/G]AGTTCATCTTTTTCC | 8065 |
rs568949167 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104575 | CATTCCCTTCATGTT[A/G]CACACTCTTTGACAG | 8065 |
rs569020075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043499 | TTAGAGGATTTAAGT[A/G]TGGGGTAATATGATG | 8065 |
rs569021865 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108093673 | TAACTGAATAAACAA[A/G]TGACTAATAGGTTGT | 8065 |
rs569027087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010317 | CTTCCTGAGGCCTCT[C/T]ATGCCTTCAGGCAAT | 8065 |
rs569035728 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042023 | GGGACTATCATGGTA[A/T]TGGGAGGGAAACGTC | 8065 |
rs569058669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099952 | TCCTCCTTCAGCCTT[C/T]CCAGTAGCTGGGACT | 8065 |
rs569082657 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108099418 | GAATAAAAACCAATT[C/G]CATTTCTATGGGGCA | 8065 |
rs569083671 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037690 | ACCCAAACTTTCTAC[G/T]GGGGGCTCGTCATGT | 8065 |
rs569120405 | in-del | -/AGG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100450 | TGGGGGTGCTGAGGC[-/AGG]AGAATTGCCTGAACC | 8065 |
rs569143916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108092937 | TTTTCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 8065 |
rs569160991 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050777 | TAAACTGCTATCTTT[A/G]TAATTTCCCTTTTAC | 8065 |
rs569192759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012404 | GGTCGATACCAAACA[G/T]TTTTCTTGTTTCTCC | 8065 |
rs569219613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108038367 | ACCTTTTACTTGCTA[C/T]AGTTAGTGGCCTCAA | 8065 |
rs569233359 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108009788 | CAGGTTTCAGTGACT[C/T]GACCCCCCACTTCTT | 8065 |
rs569278274 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022565 | CTATGTAACATCTTA[A/T]ATTTCTGGCTGATAA | 8065 |
rs569296825 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108057858 | GTTAATGTTGGGAGA[A/G]GTGAGGTGCTATTTT | 8065 |
rs569320443 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032378 | CTGGGCATGGTGGTG[C/T]GCACGTGTAGTCCCA | 8065 |
rs569322697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043926 | TACTTGGGAGGCTGA[A/G]GCAGGAGAATCATTT | 8065 |
rs569336054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108089688 | ATATGTGTGCTTAAG[C/T]AATACATTTTGGAGA | 8065 |
rs569337279 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108097821 | CTTTGTTTTTTGCAA[A/G]ATAATTGTTTTCCTT | 8065 |
rs569337839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108091206 | ACAGGTTTGTGCCAT[A/G]ACGCCTGGCTAATTT | 8065 |
rs569376757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108091706 | TCACTCACACACACA[A/C]ACACACACACACACA | 8065 |
rs569466096 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108085397 | CATTGAGACAAAAAG[C/T]AGAATAAAAGTTACC | 8065 |
rs569528264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108078033 | AAAGAACTTGCTAAA[A/G]TCTTTGACTAGGCAA | 8065 |
rs569550095 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108096953 | TGTTTGAGGACTTGT[A/G]GATTGTACTCATTAG | 8065 |
rs569605642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108075811 | AGACGTGAGCCACCA[C/T]CCCTGGCCCCCTTTC | 8065 |
rs569607097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016223 | CTAGTCAGCCAGAGA[A/G]GTTTTTCTTTTCTCT | 8065 |
rs569678547 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079114 | AATTTTAATTTATTT[A/T]TTTATTCGAGACAGG | 8065 |
rs569679068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108035079 | AGGAAAGAGAGAACT[A/G]GAGTCAGGTTATTAA | 8065 |
rs569733173 | in-del | -/TTAG | 0.00119832 | 0.0244484 | intron-variant | CUL5 | GRCh38.p7 | 11:108067741 | TGTCTTTGTTCTCTA[-/TTAG]TTATATATTGTTAGA | 8065 |
rs569741707 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081151 | AAATTAGCCAGGCGT[C/G]GTGGCTCATGCCTGT | 8065 |
rs569746098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108036865 | CAGCTGCTGGGAAAT[A/C]CTGACTGGAATGCAA | 8065 |
rs569800792 | in-del | -/AGAG | 0.00120096 | 0.0244753 | intron-variant | CUL5 | GRCh38.p7 | 11:108018684 | TGTCTTAAAAAAAAA[-/AGAG]AGAGAGAAACATCAC | 8065 |
rs569806866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043014 | GTGATGTGTCCACCT[C/T]GGCCTCCCAAAATGC | 8065 |
rs569843506 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108023899 | TCAGTGGAAAGAGAT[A/G]TTTAACTTCTTGGAA | 8065 |
rs569844914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108076355 | AATTTTACTACCTAT[A/G]GTTCTCATGCTGTAC | 8065 |
rs569852991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068635 | CCTTAATTTACAGAT[A/G]GATGATTTGTTTTTC | 8065 |
rs569855851 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047210 | TGGTTGCAGCCACTC[G/T]AGAGGCTGAGGCAGG | 8065 |
rs569877599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108062982 | TCCCAAGTAGCTGGG[A/G]TTACAGGCATGCACC | 8065 |
rs569916425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108062210 | GCTTTCTGGAATATC[C/T]TTAAATACCTCTATC | 8065 |
rs569938085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108023294 | CTTCTCCACTCTGTG[A/G]GCTGCCTTTTCACTC | 8065 |
rs569938382 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093203 | AATAGCTTTTGCCTT[C/G]TTGTGTAACTTGACA | 8065 |
rs569963677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074410 | GTGTTGGCCAGGCTG[A/G]TCTCGAACTCCTGAC | 8065 |
rs569969492 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | CUL5 | GRCh38.p7 | 11:108077270 | GGAGGGTGTGATCCG[A/C]TGTTTTTAAATGCTG | 8065 |
rs570107400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108076557 | TTTCTTCCTGTGTCT[A/G]GCTTATTTTTAAGGT | 8065 |
rs570128805 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108021554 | CAGTGGGATTATCAT[A/C]GGTCACTGCAGCCTT | 8065 |
rs570129373 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108098718 | GAGATCTTGTCTCAA[C/T]CAATTTTTTAAAAAT | 8065 |
rs570135268 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108055854 | CAGGCTGATCTTGAA[C/T]GCCTAAGCTCAGGTG | 8065 |
rs570143605 | in-del | -/TTTTA | 0.00716266 | 0.059414 | intron-variant | CUL5 | GRCh38.p7 | 11:108086965 | ATTTTTGTGTTCTCT[-/TTTTA]TTTTATTTTTTTCAT | 8065 |
rs570146574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084022 | TCATCTGTCATTAGT[A/G]TTAGTGTATTTTATG | 8065 |
rs570272754 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100718 | TCGTAGCTATGCCAG[G/T]ATAAACTCCTGGAGT | 8065 |
rs570289301 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033602 | TTCTTCACTAAACAC[A/G]TTTGTACAATTTTTC | 8065 |
rs570293384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096415 | GAAGATTGCTTGAGC[C/G]CAGGAGGATGCAGTG | 8065 |
rs570302521 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048927 | GCCTTAGCCTCCCAA[A/C]GTGCTGGGATTACAG | 8065 |
rs570316917 | snp | C/G | 1.68624e-05 | 0.0029036 | intron-variant | CUL5 | GRCh38.p7 | 11:108009387 | GGTAAGACCCTCACT[C/G]CAGCTTGGGTTTTAC | 8065 |
rs570323784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087481 | AAAAAATAAATGTAA[A/G]ACTTTCAAGCATGAA | 8065 |
rs570349401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084635 | ACAACATTACTAGTC[A/C]TATGAAGACAGATAA | 8065 |
rs570377186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108056579 | TTCTTTATAGTGATA[C/T]AAATTCAGGTTTGGG | 8065 |
rs570379611 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009017 | AAGGCTAATCCGAAG[A/G]AGTCGGGGAGGCTCG | 8065 |
rs570387851 | snp | C/G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061750 | CCATTTTCACACTGC[C/G/T]ATAAAGATAACTACC | 8065 |
rs570395847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108097922 | TTAATCAGATGTTTA[C/T]TTTTCTATATTTTTC | 8065 |
rs570397751 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108036943 | CTGGAGTGGTTCACT[C/G]TCCCCACTCCTGTTT | 8065 |
rs570423949 | in-del | -/TTTTG | 0.0525827 | 0.153383 | intron-variant | CUL5 | GRCh38.p7 | 11:108068314 | TGAAAAAACCTTTTT[-/TTTTG]TTTTGTTTTGTTTTG | 8065 |
rs570435315 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104664 | TGAATTTGATTTGTA[C/T]CCACCAGGAGAAATA | 8065 |
rs570476586 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039425 | ACAAAGATTCTCACA[-/T]TGTTTCCAGATACCC | 8065 |
rs570479841 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108015468 | ATGAGAACCTTATTA[A/C]GAACTTGTCAATTTT | 8065 |
rs570543189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108029110 | TCCAGGTATTCCCCC[A/G]TTGTCAACTCCCTGT | 8065 |
rs570561151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030611 | CACCGCGCTCCAGCT[G/T]GGGCAACAAGAGTGA | 8065 |
rs570561284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108023407 | GGTTTTAAGGTCATA[C/T]GAGTAGTTCAGATTT | 8065 |
rs570573139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030155 | GCATAAAGTTATTGT[A/G]CAAAGTATATGCCGC | 8065 |
rs570616629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017318 | TTGCTTGAGCCCAGG[A/C]GGTTGAGGCTGCAGT | 8065 |
rs570644963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108070435 | GTGTATGGTGAATTT[C/G]TACTTTTTTCTCAAA | 8065 |
rs570670204 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108049820 | TACAATTTAAATTTT[C/G]GCATGAATATGTTCT | 8065 |
rs570670268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108057762 | AAACTGGTGAAATGA[A/G]TAAGACCTAGAGTTA | 8065 |
rs570696668 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108023943 | TCCTCCTCCTCCACC[A/G]TGTTTGAAAAGAAAT | 8065 |
rs570700690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108065094 | GCAGTGGCATGATCT[C/T]GGCTCACTGCAAGCT | 8065 |
rs570746183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016839 | ACAGCTCAGGTTAAA[A/G]CTTTGGTCAGAGGCT | 8065 |
rs570776412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068766 | GGAGCAGAGATGACA[G/T]GATATCTTCTGCCTC | 8065 |
rs570792704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021601 | GCAGTGCTCTTGCCT[C/T]AACCTCTGGAGTAGC | 8065 |
rs570854282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050576 | TTTCACCATGTTGGC[C/T]AGGCTCGTCTCGAAC | 8065 |
rs570855471 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108094735 | CTTATTGATTTTTCA[C/G]CCAAAGTTACCCTGT | 8065 |
rs570878663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108014933 | AGACGGGGTCTCACT[C/G]TCTTGCCCAGGCTGG | 8065 |
rs570882882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015449 | TATGTCTAGTTAAAC[A/G]TAAATGAGAACCTTA | 8065 |
rs570892403 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008042 | TTATAGGCGTGAGCC[A/G]CGGGGCCCTATAGGG | 8065 |
rs570944248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108022630 | CTAAGCCAATTAACA[C/T]AGGACCCAAACGCAT | 8065 |
rs571005375 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108096601 | TTTTTTGAGACACTC[G/T]TGTCGCTCAGGCTGG | 8065 |
rs571013729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108026772 | GAGGTGGGCGGATCA[C/T]GAGGTCAGGAGTTCG | 8065 |
rs571030575 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061372 | AGAGAATTCTATCTA[A/G]CAATCTCCCTACTTT | 8065 |
rs571053097 | in-del | -/TTTAGTGTTC | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108080007 | TCATTCTCACCAATG[-/TTTAGTGTTC]TTTAGTGTTCTTTTA | 8065 |
rs571070924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108089780 | CGCACTGGCTCATAC[C/T]TGTAATCCCAGCACT | 8065 |
rs571100127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108090467 | CTGAACTCCAGCCTG[A/G]GTGACAGAGCAAGAC | 8065 |
rs571102821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042535 | CCCACAATTCTATAT[A/G]CTGTCGATTTTTTTT | 8065 |
rs571104857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108103417 | AAGAGAAGAAGGGGA[A/G]AAAAAAAACCTTAAA | 8065 |
rs571109760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043074 | GGCCTGTTTCTTTTT[A/T]AAAAAAATTGTTTTT | 8065 |
rs571137269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108097027 | TTAAAAGTTCCAGGT[G/T]TTTTTGTTGAGACAG | 8065 |
rs571214670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108035203 | GAAGTGGGCGAAGGG[A/G]CTACACTCTTTGTGA | 8065 |
rs571227144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108088185 | CATAAATATCCAAGA[A/G]TTTAACAGTTTTTCT | 8065 |
rs571235358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108041249 | GTAAATCTCTTATAT[C/T]AATAATCTCATTAGC | 8065 |
rs571264812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013824 | CTGTAATCCCAGCAC[G/T]TTGGGAGGATGAGGT | 8065 |
rs571266515 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108061404 | TGCCTAGGTAAAATA[A/T]TTTTCTGGAGGATTT | 8065 |
rs571288383 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053025 | CCATTAATTTCTTGG[C/T]AAGTCGTTTTAGTGA | 8065 |
rs571295200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108095747 | ATGTAGCAGGAAATA[C/T]ATGATTGGCTTGTAA | 8065 |
rs571296591 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087446 | AATTTATTTACATAT[A/C]TTTTTAGAGAAGTAG | 8065 |
rs571351204 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100833 | CAGGAGATCGAGACC[A/C]TCCTGGCCAACATGG | 8065 |
rs571361397 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108080684 | CAGGCATGAGCCACC[A/G]TGCCTGGCCCTTTTG | 8065 |
rs571592942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100768 | AGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAAC | 8065 |
rs571600837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108028650 | GAGACCAGCCTGGCC[A/G]ACATGGTGAAACCCC | 8065 |
rs571725743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108040306 | AAACACAGTGAGATT[C/G]CATTTCTACAAAAAA | 8065 |
rs571750336 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108060412 | TTTAGTTCAACTCTT[-/A]ACGTTGTAGCTGAGG | 8065 |
rs571767714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033348 | CTCCGTGTTGAGTGA[C/T]CCCCTGTGACCCCAA | 8065 |
rs571775844 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032514 | CCCTGTCTTAAAAAC[A/T]AACAAAAAACAAATC | 8065 |
rs571852743 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108027590 | TTTTTTGTATTTTTA[G/T]TAGAGACAGGCTTTT | 8065 |
rs571873240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108021148 | CCATTAGATTTGTGT[A/G]AGTACATGCTGTTAT | 8065 |
rs571960573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108040648 | AAATTAGCCAGTCGT[A/G]GTGGCACGTGCCTGT | 8065 |
rs571998673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108015024 | CTTCCTCAGCCTCCC[A/G]AGTAGTTGGGATTAC | 8065 |
rs572012479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108060813 | CTCCAGCTTGGGCAA[C/T]GAGTGAAACTGTCTC | 8065 |
rs572058053 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108067554 | CATTTTTTTTTTTTT[A/T]AAACCTGGTCACAGC | 8065 |
rs572117525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108081810 | ATGCTTAGTTCAGTT[C/G]TATTGGTTTATATAT | 8065 |
rs572126050 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057791 | TAAATTGATAGTATC[A/G]TACCAATACTATTTT | 8065 |
rs572144942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108074693 | TGCGTGTAATTCCAG[C/G]TACTTAGGAGACTGA | 8065 |
rs572209625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108055315 | ATACAGTTGACTCTC[G/T]TTTTTTGTACCGGTT | 8065 |
rs572252596 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108014401 | ATAGGAGTGAAAGGG[A/T]AGTCGGGTCAGATTA | 8065 |
rs572266968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108101556 | CATGGCACACTGTCA[C/T]TGTTCTCTGCAGAAT | 8065 |
rs572283656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108102323 | GTGAGCCACCATGCC[C/T]GGCCTATTTTTCTAT | 8065 |
rs572284640 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017815 | TTATGCTGCTGCACT[C/G]TAGCCTGGACGACAG | 8065 |
rs572286693 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076788 | TATTCAGGATTTGCT[A/G]TTGAATCAGAAGTAG | 8065 |
rs572306932 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108068297 | CATTCTTGTAGAGGA[G/T]CCTGAAAAAACCTTT | 8065 |
rs572345610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108094213 | GCAGGGACCCCTTGT[A/C]ATACCGTATTTTGTT | 8065 |
rs572346234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066998 | TGTAGCCATCACTAA[A/G]TATGTACATGCTCTA | 8065 |
rs572396612 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038634 | GAGCCAAGATTGCAC[C/T]ATTCCACTCCAGCCT | 8065 |
rs572398479 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052173 | GATGGGTCTTACTGT[A/G]TTGCCGAGGCTGGTC | 8065 |
rs572398819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108079395 | ACAGGCGTGAGCCAC[C/T]GCACCCAGTCCCAAG | 8065 |
rs572410366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108094740 | TGATTTTTCACCCAA[A/G]GTTACCCTGTATTTA | 8065 |
rs572420106 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108084958 | TAATTAATCACAACC[A/G]TTTACAGATGTAGTT | 8065 |
rs572439669 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108066353 | TGTCTCAAAAAAAAA[A/G]CCAGAGTATCATTAT | 8065 |
rs572450716 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012254 | ATCTGGGCCCTTAGT[A/G]CTCATTTTTTTCATT | 8065 |
rs572496806 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108052299 | ATATACTGCTTCCCC[A/G/T]AAGTATTCAAGTGAA | 8065 |
rs572515336 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108089236 | TCATGTAAAGTATAT[-/A]CGTTGCATTTTATAC | 8065 |
rs572573603 | in-del | -/GGGTGGGGGTGG | 0.00120773 | 0.024544 | intron-variant | CUL5 | GRCh38.p7 | 11:108019194 | TTTTGGTATCCCGAT[-/GGGTGGGGGTGG]GGGTGGGGTGGGGTG | 8065 |
rs572589103 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108006917 | AGGCGTGAGCCACCA[C/G/T]GCCAGGCCCGCTTTA | 8065 |
rs572623002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108060862 | AATCTACCATGTCTC[A/G]TAGCCTACCTGTCTC | 8065 |
rs572626822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108013225 | TTGTTTTTCACTGAC[C/T]TCCCTCCCCTGTCCC | 8065 |
rs572719457 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108045699 | AGACTGTTTCTACAA[A/C/T]AAAATTTAAAAAAAA | 8065 |
rs572724867 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030871 | AACTTCAAGAGATTC[C/T]GATCCAGTAGGCCTG | 8065 |
rs572739979 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066145 | GGAGATCAAGACCAT[C/T]CTGGCTAACACGGTG | 8065 |
rs572753400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059157 | TGCTGGGACAGTAGG[C/T]GCATGCAACCACACC | 8065 |
rs572787835 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011470 | GCTCACAAGAATTTA[A/T]AAAGTGTTTTAACTT | 8065 |
rs572834226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099080 | CACCATCTTAACTCA[C/T]TGCAGCCTCAACTCC | 8065 |
rs572835620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108093032 | TGTTAGCCAGGCTGG[A/T]CTTGAACTCCTGACC | 8065 |
rs572879968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085623 | TTAAAAAAGGAATGA[A/G]CTACTGGTACATGCT | 8065 |
rs572890940 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089015 | CAAGATAGATAGCAA[A/G]GGATGAATGAGAGTA | 8065 |
rs572915472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108092119 | TGCAGCCTGGGCAAC[A/G]GAGTGAGACCCTTTC | 8065 |
rs572954673 | snp | G/T | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007818 | TCGTCCAGGCTGGAG[G/T]GCAATAGCGCGATCT | 8065 |
rs572979096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108030908 | GTTTTAGGAATCTGT[A/G]TGTGTAATCACCACC | 8065 |
rs572994337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099593 | TGCTAAAATTTTTAG[C/T]TGTAATTTAGACACA | 8065 |
rs572999969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108086071 | AAGTGTCTAAAACCA[C/T]ATATAATTGGAGTCA | 8065 |
rs573040181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108030452 | AGACCAGCCTGATGA[A/G]CACAGAGAAACCCCG | 8065 |
rs573058737 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012053 | CACATTTTGACATAT[A/G]CAGTTAACTGCTTAG | 8065 |
rs573062648 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108082817 | TTTTTTTTTGAGACA[-/G]GGTCTTGCTGTGTTG | 8065 |
rs573094025 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032087 | ATCCTGGATAATGAA[A/G]TAATCTGTACAACAA | 8065 |
rs573146085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108037212 | AGGGGAATGAGGTAG[C/G]CAATTTTCCTGGTTT | 8065 |
rs573205526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108043255 | TTTTATTTTATTTTT[A/G]TATAGATGTGGTCTT | 8065 |
rs573238120 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108084308 | AAATGCCAGATAAAC[C/T]TTTCAGAGGTTACTT | 8065 |
rs573261696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108045829 | TGTGCCAGTGCACAC[C/T]AGCCTGGGCAACATA | 8065 |
rs573267298 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042533 | GGCCCACAATTCTAT[A/C]TACTGTCGATTTTTT | 8065 |
rs573349415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108077378 | TAGGCTGGGTGTGGT[A/G]GCTTACGCCTGTAAT | 8065 |
rs573373747 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095470 | ATAAATTCATGTCAT[A/G]GATATTAAGAGAGAA | 8065 |
rs573383178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064908 | ATTTTTCAGACAGTT[A/T]GAGTAGAATTGATAT | 8065 |
rs573448811 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108058666 | GAAAAGATCTCTGAG[A/G]GAATGATATTGGAGT | 8065 |
rs573449889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039547 | TTAATTATATTCACA[A/G]TGTTTTGCAAACATC | 8065 |
rs573457325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017634 | GTGGGAAGATCGCTT[C/G]AGCCCAGGAGTTCAA | 8065 |
rs573471101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108010633 | TAAATTAGTTAATAT[A/G]TCTATAATGCTTAAA | 8065 |
rs573487761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108068028 | CTGCCTCCCAGGTTT[A/G]AGCAATTCTCCTGCC | 8065 |
rs573512526 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108070992 | TGTTGCACTCTTTTC[A/G]AAAGGATTTATTTAG | 8065 |
rs573530642 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071196 | GTATATGTAGTATTA[A/C]AACTACCTTATGAAA | 8065 |
rs573541372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108031271 | CTCGGAGGCTGAGGC[A/G]TGAAAATCACCTGAC | 8065 |
rs573551674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108067046 | GTTGGAGGCTATGGA[A/G]ATACATACCTGGCCT | 8065 |
rs573572877 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105897 | TTTCAAGAGCATTTC[A/G]TAGGATCTGTCCCCA | 8065 |
rs573596491 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105175 | ATAGGTAGGTCATTA[C/T]GATTGCAGAGCCAAA | 8065 |
rs573638386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033676 | GCCTGTAGGGATTCC[A/G]TTATGGAAAACTGGT | 8065 |
rs573649548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108079451 | ACTTACAATAGAGTT[A/G]CTATGGTTGCTTTAT | 8065 |
rs573663998 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032169 | GTACCCCAAACTTAA[A/C]AGTTAAAGAAAATCG | 8065 |
rs573726308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032743 | TATTTAGATTTTTGC[A/G]TCTTTGTTCTCTGGT | 8065 |
rs573741505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087077 | GGATTTTTTTGTTTT[C/G]CAAATGGCTCAGGAG | 8065 |
rs573746777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108073020 | ATCCTGGCTAACATG[A/G]TGAAACCCCTCTCTA | 8065 |
rs573773136 | snp | A/G | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105138 | TTAATTGTTGCTTCA[A/G]TAGTTTAAAAAATTT | 8065 |
rs573780119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108086098 | GTCATAGAGCATAGA[A/G]AAGAGGGTATTAACC | 8065 |
rs573781743 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108093882 | CTTTTAAAATTTTTT[G/T]GTAGTGATGGGGGTG | 8065 |
rs573784993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108080154 | ATATTTTCCTTTATG[A/G]AGGGTGATCATAGCT | 8065 |
rs573831325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108073646 | GAGAACAACTATATT[C/T]GTTTTGTCTTGGCTG | 8065 |
rs573858500 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108027452 | GATTTTTGTATTTTC[A/G]GTAGAGACAGGGTTT | 8065 |
rs573865036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108017730 | TAGTGCATGCCTGTA[A/G]TCTCAGCTACATGGG | 8065 |
rs573896004 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026414 | CCCGATCTTCTCAGA[C/T]ATTGTCGTTATTTCC | 8065 |
rs573940134 | snp | C/T | 1.96845e-05 | 0.00313717 | intron-variant | CUL5 | GRCh38.p7 | 11:108078142 | TGTATATTTTCAATA[C/T]TAAAAATATTTTATT | 8065 |
rs573976789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108085471 | TACAAGATTTCTGTT[C/T]GGGATAATGAAGAAG | 8065 |
rs573999689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108011595 | TTAGAAGCCAATGTC[A/T]TAAAAAAAACCACCA | 8065 |
rs574005227 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108077438 | ATCACTTGAGGTCAG[C/G]AGTCAACATGATGAA | 8065 |
rs574029179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108025105 | CAAGATTCCAATTAT[G/T]TGTACGTTAGGTCAT | 8065 |
rs574069831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064111 | CATGTTTGAGATCTT[A/G]GAAGAAAGATTTTTA | 8065 |
rs574073044 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108071059 | GTCAATAAAATGGCA[G/T]AACATGAAAAAGTGC | 8065 |
rs574092643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031352 | CCTGGGCAACAGAAC[A/G]AGACTCTGTCTCAAA | 8065 |
rs574108508 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108063464 | TTGGTGGACAGTAAG[G/T]TTCCTTCCAAATCTT | 8065 |
rs574108541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069914 | TTTTTCCTTAGGGGA[A/G]AATACACTTTGGTAA | 8065 |
rs574121060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024413 | AGGCAACAGAGCAAA[A/G]TCTTGTCTCAAAAAA | 8065 |
rs574128848 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105938 | CTTTGTGAACTGCCT[A/G]CTGAATGGAAGGAAA | 8065 |
rs574135928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108071475 | ACCTTGTTGCCCAGG[A/C]TGATCTCCACTGCTT | 8065 |
rs574175845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059265 | TCCTGGGGAAATTCA[A/G]TTAGTATTTATTATA | 8065 |
rs574266726 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106442 | TACATTCATAGCAAA[G/T]TTTTTTATTAAATTT | 8065 |
rs574287533 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108059732 | AAAAAAAATACAAAA[A/C]AATTAGTTGGGCGTG | 8065 |
rs574288287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108099098 | CAGCCTCAACTCCCT[A/G]GGCTCAAAGGATCCT | 8065 |
rs574312744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108052413 | ACAGGCGTGCACCAC[C/T]ACACTGGGCTATTTT | 8065 |
rs574331329 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016088 | CACCCTAGGTCTGGC[A/T]AATTTTTTATAGAGA | 8065 |
rs574371431 | in-del | -/G | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106847 | CTCCAAAAAAAAAAA[-/G]AAAAATTTAATTTTT | 8065 |
rs574397724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108091330 | TACTGAGATTACAGG[C/T]GTGAGCCACCACACC | 8065 |
rs574429203 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104840 | ACTAGAAATAGCACT[C/G]TTGGTTTCTTTTGAT | 8065 |
rs574451058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015802 | ACTTCTAAAAGGAAG[G/T]GGCAGCTCAGGGTAA | 8065 |
rs574465333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010091 | GGGAGATCTAGGCCC[A/G]CAGGGGCAGATTCTC | 8065 |
rs574477108 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032313 | GGAGTTCAAGACCAG[C/T]CTGGGAAATATAACA | 8065 |
rs574480362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108049190 | TTGTCCCTATGGATA[G/T]GTCTATATTTGACAT | 8065 |
rs574489691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108104101 | ATGTTGGATAGAGGA[G/T]GAATATGCATAAAAA | 8065 |
rs574510897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108041881 | ATAGGCGTGAACCAC[C/T]GCACCAGGCCCCATC | 8065 |
rs574535269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108051720 | TCAGATTTTCAGTTG[G/T]TCCTTTTTACATTTT | 8065 |
rs574559918 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108054299 | CTGCTTCTGAATATT[G/T]ACTTACCTTACTAAT | 8065 |
rs574574055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010454 | ATGAAGAACAAATTT[C/T]ACTAAGAGGCAGTAC | 8065 |
rs574587321 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081674 | GGAGAATGGTGTGAA[C/T]CTGGGAGGCAGAGCT | 8065 |
rs574599316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050970 | TCTTTCCACTTGTAA[A/G]AATAAAATGGGACCG | 8065 |
rs574619635 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108042289 | CAGTGGTGCAGTCTC[A/G]GCTCACTGCAACCTC | 8065 |
rs574619668 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038541 | TTACCTGAGTGCGGT[C/G]GTGGGCCTCAGTAAT | 8065 |
rs574623335 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063965 | TCGTTGTAGGTAATA[C/T]CATCTGCAAACAAGC | 8065 |
rs574726838 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088093 | TCATCATTATGGAAT[G/T]TAGGTTATATTGGAT | 8065 |
rs574741709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069404 | CTGTCTGTTTCTTCT[C/G]TACCATTTTAAGCTT | 8065 |
rs574804198 | snp | G/T | 0.0023933 | 0.0345097 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009199 | CTTGGGACGAGGTCA[G/T]CGCTGTCGGCGCGCT | 8065 |
rs574814343 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030753 | GGATTTATAAGAGTA[A/T]GATGTTAATTTGTGG | 8065 |
rs574888924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108058585 | AATGAAGTAAGAGTA[A/G]TACTATAGAGTGTAT | 8065 |
rs574895954 | in-del | -/AAT | 0.000809061 | 0.0200967 | intron-variant | CUL5 | GRCh38.p7 | 11:108024429 | CTTGTCTCAAAAAAT[-/AAT]AATAATAATAATAAT | 8065 |
rs574911259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064841 | GTCTGCTTTTGGTAT[G/T]AGGGCAATACTGGCC | 8065 |
rs574915426 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092153 | AAAACAAAAAAAACA[A/C]AAAGAGATACTACTT | 8065 |
rs574930530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108096088 | GCAACAGAGTGAGAA[C/T]TCCGTCTGAAAAAAA | 8065 |
rs574989514 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108096671 | TCCAGGGTTTAAGCG[A/T]TTCTCCTACCTCAGC | 8065 |
rs575029662 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108059042 | AGTCTCGCTATGTTG[C/G]CCAGGCTGGAGTGCA | 8065 |
rs575033673 | in-del | -/CA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096115 | AAAAAAAAAATTATG[-/CA]CACACACACACACAC | 8065 |
rs575087288 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012234 | CCTTTTCTTTTGCAA[C/T]TATCATCTGGGCCCT | 8065 |
rs575148673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108023112 | GCCGGGCATGGTGGC[A/G]CATGCCTGTAATCCC | 8065 |
rs575164888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016963 | GACCTACCACCTCTA[C/T]AAAAATAAAAATTAG | 8065 |
rs575165900 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108078351 | TTGTTATTGTTAGTT[G/T]TGTGACTTTTGCAGC | 8065 |
rs575166432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108022987 | AGCGTGGTGGCTCAC[A/G]CCTGTAATCCTAGCA | 8065 |
rs575167845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108086031 | CATATTAATGGATAG[A/T]TGGAAATTGTTATCT | 8065 |
rs575213201 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022490 | TTGCTTGAAAATGCA[C/T]TCCTAAATTTCAGTG | 8065 |
rs575234269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108098734 | CAATTTTTTAAAAAT[A/G]TATTAAAAATTTCCA | 8065 |
rs575303967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108044855 | CAACCTCCGCCTCCC[A/G]GGTTCAAGTGATTCT | 8065 |
rs575327233 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096195 | AGAGAAAAGTGCTTC[-/A]AAAAAAAAGGAGAGG | 8065 |
rs575370689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108052257 | ATTAGACCACACGCA[A/G]TCGACCCTTCTTTAC | 8065 |
rs575395364 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108092062 | TGATTGCTTGAGCCC[A/C]GAAGTTCAAAGTTGT | 8065 |
rs575431285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108010516 | CTAGAATTAGACTCC[C/T]TGAATAGCCACCACT | 8065 |
rs575539942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030725 | GGATGAACTATGTTC[A/G]TGAATATAAGCAGGA | 8065 |
rs575588556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108097202 | TGTATTTTCAGTAGA[A/G]ACGGGGTTTTGCCGT | 8065 |
rs575597848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108031421 | GCTGGTGTACTAGAA[A/G]GTTAGGTTTTACATT | 8065 |
rs575615804 | snp | C/G/T | 3.44129e-05 | 0.00414795 | intron-variant | CUL5 | GRCh38.p7 | 11:108050099 | CTTGTTTTCCTAATA[C/G/T]TCTTCAGAAAGAGGG | 8065 |
rs575662359 | snp | G/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108082457 | GGCTATATTATTTTT[G/T]GTAGAGACAGTCTCT | 8065 |
rs575698531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108043217 | TAGGACTACAGGCAT[A/G]TGCCACCATGCCCAA | 8065 |
rs575702509 | in-del | -/G | 0.0182019 | 0.0936463 | intron-variant | CUL5 | GRCh38.p7 | 11:108037691 | CCCAAACTTTCTACT[-/G]GGGGCTCGTCATGTA | 8065 |
rs575739820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108077179 | GAAAAATGAGGAGTC[A/G]TCTTTCATGAGAAGG | 8065 |
rs575748853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090139 | TTCTTGAGTTGTTTC[C/T]ACTGTTTCACTCCCA | 8065 |
rs575774831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084149 | TTATTTGGGAGACTT[A/G]CTTCTGAGGAGGAGT | 8065 |
rs575803979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108070752 | TTTAACATTTTTTTG[C/T]TTTTGTTTTTTAAAT | 8065 |
rs575811528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090645 | TGATGGCCTATTTAG[A/G]GTAATCAATGCTGAT | 8065 |
rs575811657 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108083614 | AGGGCAATGTAGTGA[A/G]ACCCATCTCTACAAA | 8065 |
rs575864902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015080 | ATTTTTGCATTTTTA[A/G]TAGAGATGGGGTTTC | 8065 |
rs575890522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016394 | CACCTCATCCTCCCA[C/T]AGGTGCAACACCAGC | 8065 |
rs575951414 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009255 | GCGGGCCGACGGGCC[C/G]TGGGCCCTGGTGGGA | 8065 |
rs575951535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108015642 | GTGTCTGTGTTGGTC[A/G]TGGGTAGGAATGGGA | 8065 |
rs575988336 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106857 | AAAAAAAAAAATTTA[A/G]TTTTTAAAAATTAGT | 8065 |
rs575988925 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108049540 | TGGAGATGAGGTCTT[A/G]CTATGTTGCCCAGGT | 8065 |
rs576006191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108060937 | CTTATTGGAGTGCCT[G/T]CTGTGTTTTATAGCA | 8065 |
rs576042538 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108067749 | TTCTCTATTAGTTAT[A/G]TATTGTTAGATTTAC | 8065 |
rs576044435 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108060491 | AAATGCTTTTTTTTT[A/T]AAACGAAATTTGAGC | 8065 |
rs576048492 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079673 | AGATTTGACAAATGC[A/C]TATACCCCTATTAAC | 8065 |
rs576080831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108035316 | ATCAGCAGCTTGATT[C/T]TGGATAGTCCCATCA | 8065 |
rs576084336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108021994 | TATCTATCTGTATCT[A/G]TCTACCTATCTATCC | 8065 |
rs576094924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108028697 | AAAAATTAGCTGAGC[A/G]TGGTGGTGCACACCT | 8065 |
rs576099112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068398 | ATCAAGGCTTACTGC[A/G]GCCTTGACCTCCTGA | 8065 |
rs576106390 | snp | C/T | 0.000121079 | 0.00777977 | intron-variant | CUL5 | GRCh38.p7 | 11:108094799 | TTTATATTCCTGATA[C/T]TCTTCTCTATAGCTG | 8065 |
rs576134954 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018163 | GGCCTGAGGTGGCAT[C/T]GGAGCTGAGACCTGA | 8065 |
rs576147627 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040060 | CTTGCTGCTTTTCCT[G/T]TCGCTTCTGTCTGCC | 8065 |
rs576162049 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081873 | TTACTGTAGCCTTGC[A/G]ATAAGCTTTAAAAGC | 8065 |
rs576175226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069263 | GCAGCAGAGCAAGAC[C/T]CTGTCTCTTAAACAA | 8065 |
rs576181723 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058920 | AAGGTAAGAGGCTTC[C/T]GAGCTGTGCTGCTGA | 8065 |
rs576268482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087849 | GGGCACCTGTAATCC[C/T]GGCTGCTCTGGAGGC | 8065 |
rs576281263 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108096122 | AAAATTATGCACACA[A/C]ACACACACACGAGAT | 8065 |
rs576292361 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108089097 | AAGCCCAGGAATACA[A/T]ACAAGAAAAAAAATA | 8065 |
rs576319705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108062638 | TATTTATGGGTTACA[G/T]GAGACATTTTGATAC | 8065 |
rs576331052 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108088385 | TAAATTAGGCACCCT[A/G]GGATGCTTGCTTATC | 8065 |
rs576439344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108103554 | CCCCACCTGACCTGT[A/G]CTGCTATACAAAGAA | 8065 |
rs576440878 | snp | C/G | | | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074152 | AACTTTCTCCATTCT[C/G]CAGTAGGATTTTTTT | 8065 |
rs576461284 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108075930 | CACCATCTGACATAG[G/T]TACTCATTTTCTTGT | 8065 |
rs576473787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108012813 | TATTGGCCAGGATGG[C/T]CTCAAACTCCTGACC | 8065 |
rs576474186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108100884 | AATACAAAAAACTAG[A/C]CAGGTGTAGTGGTGC | 8065 |
rs576524849 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108103232 | AAGAAAAATTTTGAT[A/T]AAATGACCTAGATGA | 8065 |
rs576540194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048334 | TTTTATTTGTTCACA[A/G]TTCTGTGGCTTAGCA | 8065 |
rs576602926 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058307 | AGGCTAGAGTGCAGT[A/G]GTGCAGTCTCCGCTC | 8065 |
rs576604270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108014079 | AAGGCAAAAGTTTCA[A/G]ATGTGTTACCAACTG | 8065 |
rs576719573 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108087653 | TTTTTTAAAAAAACA[A/G]TATGCTCTGTTTAAA | 8065 |
rs576745445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108097296 | GCTGGAATTACAGGC[A/G]TGAGCCACTGCACTT | 8065 |
rs576767022 | in-del | -/AG | 0.00239904 | 0.0345509 | intron-variant | CUL5 | GRCh38.p7 | 11:108018686 | TCTTAAAAAAAAAAG[-/AG]AGAGAGAAACATCAC | 8065 |
rs576768858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069355 | TTTTCATTCATAATC[C/T]GGTTGCAGCCTATCT | 8065 |
rs576794149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042035 | GTAATGGGAGGGAAA[C/T]GTCCACATTAGAGAG | 8065 |
rs576820839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108055156 | GGAGCTGGTATGCAA[A/G]ATCAAATCTATTTGC | 8065 |
rs576830104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108063286 | AGCTTCCACAAATGA[A/G]TGAGATCGTGTGAAG | 8065 |
rs576856835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108041461 | TTTGTATTTTTGGTA[A/G]AGACGGGGTTTCACT | 8065 |
rs576977521 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032493 | AGCCTGGGTGACAGA[A/G]CAAGACCCTGTCTTA | 8065 |
rs576979176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108059600 | TAAAATGGAATAGGC[C/T]GGGCGCGGTGGCTCA | 8065 |
rs576983948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064045 | CTGATTCCTCTAACT[A/G]CAACTTCCAGTATTA | 8065 |
rs576999533 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108016261 | TCTTCTCGTCTTCTC[A/T]TCTCTTCTCTTTTCT | 8065 |
rs577004355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108009725 | TCAGTTTCTTGTAAA[A/G]CAATGTCTAAGACGC | 8065 |
rs577024483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108022948 | TTCTTGGATATACAT[A/G]TTAGAAATATCCTTT | 8065 |
rs577042350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048963 | AGCCACCGCACCTGC[C/T]GTGACTCCACCACCT | 8065 |
rs577049297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090828 | AGATATTTTAACTTA[C/T]AGCTAGCCCTTCGCA | 8065 |
rs577092971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108083312 | TTAACTGGTCCTTTA[C/T]TGCTGCATTAAGTAG | 8065 |
rs577102144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050303 | ACCATTATCTCCTTT[A/C]CTTTTCCTTTTTACT | 8065 |
rs577104126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108058049 | CCCTGTCTCTACTAA[A/G]AATACAAAAATTAGC | 8065 |
rs577126157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108082538 | CACCTTAGCCCCTCA[A/G]AGTGCTAGGATTACG | 8065 |
rs577186894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108061675 | TTCCCTCCTGCATTC[C/G]TATATTTAAAAATAA | 8065 |
rs577239784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068832 | ACCCTTGCTATCTTA[C/T]CTGAAATAGTTCAAC | 8065 |
rs577242375 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015351 | GTCAGGATCATGCTT[C/G]GCAAGGAATATGGAT | 8065 |
rs577249384 | snp | A/G | 1.65026e-05 | 0.00287246 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108088608 | GCTAAGAAAAACACC[A/G]TTAAGCAAAAAACTA | 8065 |
rs577286537 | snp | C/T | 7.6859e-05 | 0.00619868 | intron-variant | CUL5 | GRCh38.p7 | 11:108095517 | TATTAAAAATCTGTT[C/T]TATCTATTATAGATA | 8065 |
rs577295887 | in-del | -/G | 0.00119784 | 0.0244435 | intron-variant | CUL5 | GRCh38.p7 | 11:108083117 | CTAATTGCTCTGACC[-/G]GGAACGTCTACTACA | 8065 |
rs577296662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108048426 | GACATGGTGGTCTAA[A/G]AGAGCATTAAAACTC | 8065 |
rs577314911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108020387 | AGTGATGATGATCCT[A/G]ACCCTGTGGAGGCCT | 8065 |
rs577325882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108042105 | TAAGGGATAAAAGGG[A/G]GTTAGTTTGCCCAAT | 8065 |
rs577352610 | in-del | -/TAG | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108070829 | GTCCTGTTTAATCTC[-/TAG]TAGTTGCATTTAAAG | 8065 |
rs577371522 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009077 | GTCGGCTCCCGTTAC[C/T]TTCTCAGCATTCGCC | 8065 |
rs577383422 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108041638 | TCTTGTTGCCTAGGC[C/T]GGAGTGCAGTAGCGT | 8065 |
rs577385252 | in-del | -/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008113 | TTATCACAACTCCCA[-/C]CTAAGTAATATTTGA | 8065 |
rs577391506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108027473 | GACAGGGTTTCACCA[C/T]GTAGGTCAGGCTGGT | 8065 |
rs577416371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108089147 | ACAGAAAGGCCGAGA[A/G]AGATGACTAGTGTCA | 8065 |
rs577438388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102249 | TGGCCGGGCTGATCT[A/C]GAACTCCTGACTTCG | 8065 |
rs577450969 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108036067 | AAATATGCACATCAG[G/T]CTGGAAAATCATCAG | 8065 |
rs577473693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108061076 | TGGATTTAGAAGTTG[G/T]GCTCATCTCAGGCAA | 8065 |
rs577512852 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108035441 | TATCTTTTAAATATT[A/C]AGTAATCTTTGACGG | 8065 |
rs577597148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028869 | CACTTCTTGCTCAGA[A/G]TCTTTTAATGGCTCT | 8065 |
rs577625266 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108044507 | AGTGAGACAGTGTCT[-/C]AAAAAAAAAAAAATT | 8065 |
rs577645953 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063811 | TTTGAGGAACCTCCA[A/G]ACTGCTCCATAGTGC | 8065 |
rs577678361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108087675 | CTGTTTAAATTGTTA[C/T]CAGGAGCCAGGTGCG | 8065 |
rs577712409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108040473 | AAAAATCGGCTGGGT[G/T]TGGTGTTGTGCACCT | 8065 |
rs577734677 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034034 | AAGTATTACTAGTTA[A/C]ATTGAGGGTCTCCAA | 8065 |
rs577748506 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017050 | GTGTAGCTGTGGTTT[A/G]TTCATTCCATAAAAA | 8065 |
rs577761170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108087128 | TATAATAAGAAAAAC[A/G]TATTCTAGTCTCATC | 8065 |
rs577774605 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107232 | AAAATGAAATGTTAG[A/C]TTTCTTTCTTTTACT | 8065 |
rs577783981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108081166 | GGTGGCTCATGCCTG[C/T]GATCCCAGCTACTTG | 8065 |
rs577795495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108073883 | GCAGAGTTGATTCCT[C/T]CATCCTCCGTCCTTT | 8065 |
rs577820697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108080339 | AGAGATGCTCCTGCC[C/T]CAGCCTCCCAAAGTG | 8065 |
rs577824130 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108048911 | ACCTCGTGATCTGCC[C/T]GCCTTAGCCTCCCAA | 8065 |
rs577826407 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108068212 | CTATGAGCCACCACG[C/T]CCAGCCATGTGTATT | 8065 |
rs577865060 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085432 | GATGGGGAAGGGGGG[A/G]ATGGGAAGTTACTGT | 8065 |
rs577942701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108025296 | GTGATTTTTTTTGTC[C/T]TGGTGATAGTTTATA | 8065 |
rs577950268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108072278 | AACTAATGTTTCTCT[A/G]AACTCTTACTCTAGT | 8065 |
rs578000965 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066320 | CTGCACTCCAGCCTG[G/T]GCGACAGAGCGAGAC | 8065 |
rs578039373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108025839 | CTCTGCCTCTTAAAT[A/G]TAGTGAAACCCCTAG | 8065 |
rs578168019 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023233 | CAGCCTGGGCAACAA[A/G]CAAAACTCTGTATCA | 8065 |
rs578203668 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108060252 | AGACTTTTGTAGTGC[C/T]ACTAATGATAGTAGT | 8065 |
rs578214361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108053168 | ATGTAGGAGTACATT[C/T]TCTCTTACTTCTAAT | 8065 |
rs578258153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108053827 | GGGACTGCAGGCATG[C/T]ACCACCACACCTGGC | 8065 |
rs745307081 | in-del | -/AAAAAAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040612 | GTGAGACTCCGTCTC[-/AAAAAAA]AAAAAAAAAAAAAAA | 8065 |
rs745310537 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019624 | CACTCGTGTCTGTGG[C/T]GATGCTGGTGTACAT | 8065 |
rs745318558 | snp | C/T | 5.05548e-05 | 0.00502741 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033797 | TTATCTTTTTTTTTT[C/T]CAAGAATAAAGGTTC | 8065 |
rs745385185 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098035 | TTTATTCAGAGAAAG[C/T]GTTTTTTGTGTTGTT | 8065 |
rs745406143 | snp | A/G | 1.65244e-05 | 0.00287436 | missense | CUL5 | GRCh38.p7 | 11:108072362 | TTTCATTGATGGACA[A/G]AGTTCCTAATGGTAT | 8065 |
rs745431124 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032555 | ATTTAACTTGAAAAG[A/G]AGTACTAATGACTAA | 8065 |
rs745435331 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051546 | GAGTGTTATAAAACT[C/G]TTAACTCTTGTTGTT | 8065 |
rs745437624 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108062794 | TTTTACTGTAGTCAC[C/G]CTGTTATGTTATCAA | 8065 |
rs745460208 | snp | A/T | 3.31857e-05 | 0.00407329 | synonymous-codon, intron-variant | CUL5 | GRCh38.p7 | 11:108104354 | CAGAAGAGATGAATC[A/T]GATATCAACACTTTC | 8065 |
rs745481288 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083891 | CTAGAACAAGCTTGT[C/G]CAACCCTGCGGGCTG | 8065 |
rs745483560 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036925 | GCTAGTCTGAAGAAA[C/T]AGCTGGAGTGGTTCA | 8065 |
rs745491818 | snp | A/C | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007902 | TCCCGAGTAGCTGGG[A/C]TTACAGGTGCCCGCC | 8065 |
rs745497182 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052383 | GCAGTGGCGTGGTCT[C/T]GGCTCACTGGGACTA | 8065 |
rs745540137 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008800 | ATTTGGGGCGGGGTG[C/T]CGGAAAACGCCAGGT | 8065 |
rs745573223 | in-del | -/TTATTC | 2.3733e-05 | 0.00344469 | intron-variant | CUL5 | GRCh38.p7 | 11:108073343 | TCTCATTTTTTTGTG[-/TTATTC]TTTTTCTTTTAAAAA | 8065 |
rs745576081 | snp | A/G | 2.04652e-05 | 0.00319878 | intron-variant | CUL5 | GRCh38.p7 | 11:108104154 | TTAAAATAATTTCGT[A/G]TATTAATGCGCTTTT | 8065 |
rs745622794 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087576 | GCCTGGACAATATAG[A/G]TAGTGAGACCTTGTC | 8065 |
rs745660927 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033787 | AAACTCCCTTTTATC[-/TT]TTTTTTTTTCAAGAA | 8065 |
rs745675408 | snp | A/G | 4.11862e-05 | 0.00453777 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094504 | CAAAAATAATAAATT[A/G]GCATTACCAGGTATT | 8065 |
rs745735371 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088741 | GACTTTCTGTGATAG[C/T]ATCAATTTAAAAATG | 8065 |
rs745740751 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076601 | GTCATATATATGTAC[C/T]AGTTTCTTTATCCAT | 8065 |
rs745772928 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030037 | TTCTATGGTTCTTTC[A/T]TATTTGTTTATTTGC | 8065 |
rs745775531 | snp | G/T | 1.6741e-05 | 0.00289314 | intron-variant | CUL5 | GRCh38.p7 | 11:108070233 | TAATCTTCTAAGAGG[G/T]TATCTTTGAAACAAA | 8065 |
rs745781600 | snp | C/T | 1.65214e-05 | 0.0028741 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094939 | ATTCTACAAAAAAAA[C/T]CATAGTGGTAGAAAA | 8065 |
rs745818099 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064657 | GGAGCTTGCAGTGAG[C/T]CAAGATCATGCCACT | 8065 |
rs745819667 | in-del | -/AAG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048493 | TGGTTTGTCATTCTC[-/AAG]GAGACCAGCCTTTGA | 8065 |
rs745827805 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031166 | TGAATCCAGGAGTTC[A/G]AGACCAGCCTGGGCA | 8065 |
rs745835884 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018410 | GATGGCGCATGCCTA[A/T]AATCCCAGCACTTTG | 8065 |
rs745871372 | snp | A/T | 1.70685e-05 | 0.00292129 | intron-variant | CUL5 | GRCh38.p7 | 11:108094807 | CCTGATATTCTTCTC[A/T]ATAGCTGATTCAGTT | 8065 |
rs745884395 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065477 | TCAAGTCCTTACCAC[C/T]GGAATGGGCGATTCC | 8065 |
rs745894027 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022940 | GAGAGCCTTTCTTGG[A/G]TATACATATTAGAAA | 8065 |
rs745905457 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034971 | ATCATTTATCTAGTG[C/G]GTAGCCTAGAAAACA | 8065 |
rs745976190 | snp | A/G | 2.31898e-05 | 0.00340505 | intron-variant | CUL5 | GRCh38.p7 | 11:108073514 | TATATATTCCTATAT[A/G]TATAAAAAACACTTT | 8065 |
rs745980053 | in-del | -/AAAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016798 | TGTACAAAAACAAAC[-/AAAA]AAAAACAAACAAAAA | 8065 |
rs745986939 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093303 | TTATCTTTTGGGCTG[C/T]CAGTGTCATGAAATA | 8065 |
rs745998886 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068536 | AATCCCCATTACCTA[A/G]ATTCAGCTTTAGTAG | 8065 |
rs746018900 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069550 | TCTAAGTTTTTTTTT[A/C]TTTTGTGTGTGTTTG | 8065 |
rs746046548 | in-del | -/TTTTTTTT | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007755 | TTTTTTGTTTGTAGT[-/TTTTTTTT]GTTTTTTTTGTTTTT | 8065 |
rs746069302 | snp | C/T | 5.10573e-05 | 0.00505233 | intron-variant | CUL5 | GRCh38.p7 | 11:108050084 | AAGACTATTTTTCTC[C/T]TTGTTTTCCTAATAT | 8065 |
rs746104114 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098045 | AAAGCGTTTTTTGTG[-/T]TTGTTTTGTTTCGTT | 8065 |
rs746145969 | snp | A/G | 9.95619e-05 | 0.00705486 | missense | CUL5 | GRCh38.p7 | 11:108078191 | GCGTATAAAGCAGTT[A/G]TTAATGATGCTACCA | 8065 |
rs746159946 | snp | C/T | 5.17522e-05 | 0.00508659 | intron-variant | CUL5 | GRCh38.p7 | 11:108049872 | TTTATTTCAAATTGG[C/T]ACACCTCTTTTTTTC | 8065 |
rs746180978 | snp | A/C | 1.67764e-05 | 0.00289619 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054927 | TACGTTATTTAGAAA[A/C]AAGACGAGAATGTAA | 8065 |
rs746209412 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051472 | GTACCTATATCAAGA[G/T]TATGAGGATTAAATG | 8065 |
rs746230751 | in-del | -/TGA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071168 | ATGTTTTTTACCTTT[-/TGA]TGATATGGCTGTATA | 8065 |
rs746237135 | snp | G/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107429 | GTTTTTCTGTTCTCA[G/T]GTAAGTGACTGGGAT | 8065 |
rs746245051 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092343 | GACCCAGCAATTTCA[C/T]TCTTAGGTAATTCAT | 8065 |
rs746323543 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025711 | CTTACAGTTTTCTCA[C/T]ACCCAGGTACAGGTT | 8065 |
rs746375475 | snp | C/G | 1.70519e-05 | 0.00291987 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009319 | GCCACGAATTCTCGC[C/G]TCGTCTCGCGAGAGT | 8065 |
rs746414948 | in-del | -/CAT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108046812 | AATTCAGCACTCTTA[-/CAT]CATTGCTGTTATGTA | 8065 |
rs746420385 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023476 | AAACAAAATTTTAAA[A/G]TTCCTTTTATAGATT | 8065 |
rs746443896 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029941 | CAAAAGTGCTTGTGG[A/C]AATAGACTTAATTGA | 8065 |
rs746467613 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017239 | CAAAAAATAAAAAAT[A/G]AATACCTGGGGGTGG | 8065 |
rs746498405 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059798 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 8065 |
rs746498757 | in-del | -/AAAAAC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064711 | TGATACTCTGTCTCA[-/AAAAAC]AAAAACAAAACAAAA | 8065 |
rs746507663 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053849 | ACACCTGGCTAATTT[-/G]TTTCTTTTTTTTTCT | 8065 |
rs746511896 | snp | A/G | | | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108107956 | AAAATGAGAGCAGTC[A/G]GGAATGTAGCTTTTC | 8065 |
rs746530165 | snp | C/T | 1.68156e-05 | 0.00289957 | synonymous-codon, intron-variant | CUL5 | GRCh38.p7 | 11:108104375 | CAACACTTTCATATA[C/T]ATGGCATAATTTTGA | 8065 |
rs746541449 | snp | G/T | 1.67461e-05 | 0.00289357 | intron-variant | CUL5 | GRCh38.p7 | 11:108033935 | CCCACTAATTCTGTT[G/T]GCTAGCATAAAGGAA | 8065 |
rs746554488 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023094 | CTCTACTAAAAAAAA[-/T]TAGCCGGGCATGGTG | 8065 |
rs746590831 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108049730 | CTGCTGTGAACATTC[A/G]TGTACAAGTTTTTTT | 8065 |
rs746634507 | snp | A/G | 1.93377e-05 | 0.00310942 | intron-variant | CUL5 | GRCh38.p7 | 11:108089626 | AGAGTGGCTAAGAGT[A/G]AGTAAATTTTTTTAA | 8065 |
rs746662822 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035475 | GACAAAGTGGCTTAC[A/G]CCTGTAATCCCAGAA | 8065 |
rs746673902 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051433 | TACCCCAGGTTTCAC[A/G]TATCTAAAGGGGGGA | 8065 |
rs746675068 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099271 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGTGT | 8065 |
rs746719682 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011090 | TGCTATTAATTGAAA[C/T]GTGTTTAAGAAGTAA | 8065 |
rs746722518 | snp | A/G | 3.89529e-05 | 0.00441304 | intron-variant | CUL5 | GRCh38.p7 | 11:108088700 | TTTTAAAATTACCTT[A/G]CTTTGAATTTGTGTT | 8065 |
rs746739427 | in-del | -/TTCCTTC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101882 | CTGAAGGAACACACT[-/TTCCTTC]TTCCTTCTTCCTCTC | 8065 |
rs746817524 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008727 | TATGCACGAGTTATT[A/G]AAGACAGCTGTTGTA | 8065 |
rs746820798 | snp | A/G | 1.68843e-05 | 0.00290549 | intron-variant | CUL5 | GRCh38.p7 | 11:108095010 | GATAGTGTGTTAGTT[A/G]TTTCAGCTTTCAGTT | 8065 |
rs746820875 | in-del | -/T | 1.67798e-05 | 0.00289648 | intron-variant | CUL5 | GRCh38.p7 | 11:108078165 | TTTTATTCCAAATTA[-/T]TTTTTTGCAGGCGTA | 8065 |
rs746835315 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101737 | ATCAAATGGGGACCA[A/G]GGCCAGTGTCCCTCT | 8065 |
rs746862261 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086324 | AATATAAGACTAATA[A/G]CTAGCTTGTAATCCC | 8065 |
rs746863461 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056014 | GAACTCCTGGCCTCA[A/G]GCAATCCTTCTTGCT | 8065 |
rs746863813 | snp | A/G | | | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108108261 | AAAAATTAGCCGGGT[A/G]TAGTAGCGCGCGCCT | 8065 |
rs746911462 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087445 | AAATTTATTTACATA[C/T]ATTTTTAGAGAAGTA | 8065 |
rs746913542 | snp | A/G | 2.38376e-05 | 0.00345228 | intron-variant | CUL5 | GRCh38.p7 | 11:108073340 | TTTTCTCATTTTTTT[A/G]TGTTATTCTTTTTCT | 8065 |
rs746929872 | snp | A/G | 1.6507e-05 | 0.00287284 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033831 | TCAGTTTGAAGACAA[A/G]TGGGATTTTATGCGC | 8065 |
rs746943462 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040486 | GTGTGGTGTTGTGCA[C/T]CTGTAATCCCAGCTA | 8065 |
rs746997182 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029049 | AAGCATGTTTCTATC[G/T]TATGTTCTTTGCATT | 8065 |
rs747012091 | snp | C/T | 0.000116001 | 0.00761491 | intron-variant | CUL5 | GRCh38.p7 | 11:108089478 | AACTGAAAGTAACTT[C/T]ATTTTTCATACAGCT | 8065 |
rs747028571 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022894 | GTTTTGCTTTTCTTA[C/T]GGACTTTTTAGTTCT | 8065 |
rs747083187 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092273 | GGAGACATAAGATGG[C/T]GCAGACACTTTGGAA | 8065 |
rs747136692 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081039 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA | 8065 |
rs747145971 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032432 | AGAATTGCTTGAGCC[C/T]AGGGGATCAAGGCTA | 8065 |
rs747147088 | snp | C/G/T | 3.32343e-05 | 0.00407631 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094846 | AATTCTGAATGCTGG[C/G/T]GCCTGGTCAAGAAGT | 8065 |
rs747173017 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020233 | CTAATAAATTTAAAA[C/G]TTAACTGTAAAATAG | 8065 |
rs747176840 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079576 | ACTTCAGCATACAGT[C/T]ATTTATTGAATTTAA | 8065 |
rs747184386 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067447 | TAGAATATACTGTTT[A/G]TTTGTACATATCTGA | 8065 |
rs747220139 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108021549 | GAGTGCAGTGGGATT[A/G]TCATAGGTCACTGCA | 8065 |
rs747245476 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068482 | TCTTTATTCGGAAAA[C/T]TTTAAGCATTTTTAC | 8065 |
rs747259367 | snp | C/T | 0.000302424 | 0.0122931 | intron-variant | CUL5 | GRCh38.p7 | 11:108052655 | ATTTGTTCTTGTTTT[C/T]CTAGCTTATGCTTGA | 8065 |
rs747310876 | snp | C/T | 1.68422e-05 | 0.00290187 | intron-variant | CUL5 | GRCh38.p7 | 11:108009383 | TAAAGGTAAGACCCT[C/T]ACTCCAGCTTGGGTT | 8065 |
rs747381260 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071473 | CCACCTTGTTGCCCA[A/G]GCTGATCTCCACTGC | 8065 |
rs747383106 | snp | A/G | 1.64893e-05 | 0.0028713 | missense | CUL5 | GRCh38.p7 | 11:108097711 | TCACCCAAAGACTTT[A/G]CAGAAGGTACCCTCT | 8065 |
rs747399744 | snp | A/C | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007265 | GGCTGAGTTTTGACA[A/C]GTGCATACACCTGAA | 8065 |
rs747423113 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060082 | TTAAAAAGCTGAATA[A/G]GCAACTAGGTCACAA | 8065 |
rs747471709 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027596 | GTATTTTTAGTAGAG[A/G]CAGGCTTTTTCCATG | 8065 |
rs747517524 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014743 | GATGAACTAGGCAGA[C/T]AGCTCCTGCCCTTGT | 8065 |
rs747518582 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108045560 | ACTGCACTCCAGCCT[A/G]GGTGACAGAGTATAT | 8065 |
rs747600200 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027993 | CTCTCTCCGCCTCTT[A/T]ATGTTGGATATCTAA | 8065 |
rs747668145 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040424 | CGATACCACCCTGGT[A/C]AACATGGTAAAACCC | 8065 |
rs747756276 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061544 | CTACCCCCATACCCA[C/G]TCTTCCAGATTCAAC | 8065 |
rs747767231 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028956 | GATCCAGCTCAGTAA[G/T]ATCCAGTAAGCTAAG | 8065 |
rs747809387 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063304 | AGATCGTGTGAAGTT[C/T]GTCTTTCTGTTCCTG | 8065 |
rs747811252 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047937 | ATGCTGAACACTGGC[A/G]AAAAAAAGTAGGGGA | 8065 |
rs747830548 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057085 | TACTGCAATTTGTAT[A/G]TTAGTCATATCATAG | 8065 |
rs747839200 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108021119 | TAGCCTAAGTGTATA[C/G]TAAGTAGTCTCTACC | 8065 |
rs747860270 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066017 | ATCTTTCATAAACAT[-/C]ACTTTTATTGTTTTA | 8065 |
rs747921369 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038743 | CAGTGTATCGTCCTT[C/T]TAGGTAAAGGGATTT | 8065 |
rs747986049 | snp | A/C | 2.22324e-05 | 0.00333402 | intron-variant | CUL5 | GRCh38.p7 | 11:108073361 | TTCTTTTTCTTTTAA[A/C]AACTTAATGTAAAAC | 8065 |
rs748014009 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036057 | ATCTGCTCAAAAATA[G/T]GCACATCAGGCTGGA | 8065 |
rs748026436 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067174 | ATGAGGTTGCCATGT[A/G]GGTTAAATGAGATCT | 8065 |
rs748034826 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065138 | TCACACCATTTTCCT[G/T]CCTCAGCCTCCCAAG | 8065 |
rs748095382 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009847 | AAATTCCGAGTCAGA[C/T]CAGCAGTGCCTCCCA | 8065 |
rs748110667 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022532 | TTTTTTTTAAGCAGT[A/G]ATATGTTCTAGAAAG | 8065 |
rs748128652 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041009 | TCTGACATATATGCA[A/G]AAGTGATTTGAGTAC | 8065 |
rs748146987 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010859 | ATCTCAGCTCTTTGA[C/G]AGGCCAAGGTGGGAG | 8065 |
rs748149662 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039374 | GTGTCTTTCTCCTCA[C/T]CCTTCTGTGTCTTTC | 8065 |
rs748180115 | snp | A/G | 1.69066e-05 | 0.00290741 | intron-variant | CUL5 | GRCh38.p7 | 11:108033951 | GCTAGCATAAAGGAA[A/G]TTTTAGTGATGTCTT | 8065 |
rs748236348 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072283 | ATGTTTCTCTAAACT[C/G]TTACTCTAGTAAATG | 8065 |
rs748248728 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092136 | AGTGAGACCCTTTCT[C/G]AAAAACAAAAAAAAC | 8065 |
rs748310745 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108078056 | CTAGGCAAATTCTGT[C/T]TGGCCAGATATACCA | 8065 |
rs748313199 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090893 | CTGAAACTGCTTAGT[A/G]GGAAAAAGAATGATT | 8065 |
rs748344260 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108045124 | GTATTAAATATATTT[C/T]TATAATGAAGAACTT | 8065 |
rs748378477 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031317 | CTATAGTGAGCCAAG[A/C]TTATGCCACTGCACT | 8065 |
rs748391351 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020079 | TGAGGGATCCACCAC[C/T]ATGACCCAACACTTT | 8065 |
rs748396581 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085288 | TGCTACAAGGTAGAT[A/G]AACCTTGAAAACATG | 8065 |
rs748475241 | snp | C/T | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007489 | GAGAAAGAGTGAAAA[C/T]AGGAGATGGCAGATA | 8065 |
rs748500386 | snp | C/T | 1.65132e-05 | 0.00287339 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108097746 | AGTGAACCAGGAGTT[C/T]AGTTTAATGTAAGCT | 8065 |
rs748502318 | in-del | -/T | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007150 | CTGGTCTCGAACCCC[-/T]GGGCTCAAGTGATCT | 8065 |
rs748533749 | in-del | -/TTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012524 | TATGTCCCCTCTTAC[-/TTT]TTTTTTTTTTTTTTC | 8065 |
rs748541065 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071357 | CCTTGACCTCCTGGG[C/G]TCAAGCGATCCTCCC | 8065 |
rs748580280 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036759 | GTTGGGATTACAGGC[A/G]TGAGCCACGGTGCCC | 8065 |
rs748609429 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069932 | TACACTTTGGTAAAC[A/T]AGTATAGCATATCCA | 8065 |
rs748626900 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013691 | CAAACTTTAAACTGA[A/T]ATATGATTCATACTA | 8065 |
rs748631256 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037992 | TGGGCTATTGTAATC[A/G]TTTTCTCTCTTTATC | 8065 |
rs748633206 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025204 | TTTTTGGTCATATAG[A/C]ATATGTATAGTAGCT | 8065 |
rs748662907 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059165 | CAGTAGGCGCATGCA[A/G]CCACACCCAGCTTTA | 8065 |
rs748697204 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069895 | AGAGTCTAGTTCTAT[A/G]GTTTTTTTCCTTAGG | 8065 |
rs748706467 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009645 | AGGGACCAGCTCTGG[C/T]CGGGAGCGGGAGATG | 8065 |
rs748710112 | snp | C/T | 0.000166842 | 0.00913198 | intron-variant | CUL5 | GRCh38.p7 | 11:108088519 | ACTGCTTTTAATTTG[C/T]TTTTTAGGGTGGGAT | 8065 |
rs748718794 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099468 | AATAAGAAAAATACA[C/T]ACACATTTTTTAAAA | 8065 |
rs748735377 | in-del | -/AC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072490 | CAATGGCAATGATAG[-/AC]ATATATATCAAGGCT | 8065 |
rs748748871 | in-del | -/A | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106933 | CCCATCTTCTAGTTT[-/A]AAGACAGAGACATCC | 8065 |
rs748759725 | snp | G/T | 1.81602e-05 | 0.00301326 | intron-variant | CUL5 | GRCh38.p7 | 11:108054975 | GTAATTTTGTAATTG[G/T]ACATTTTATGGGATT | 8065 |
rs748787040 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076660 | TTTGCTATTGTTAAT[A/C]ATGCAGTGAATGTGG | 8065 |
rs748808666 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085083 | CTGAGGTGTATACCA[A/G]AGAGAAATGAAAACA | 8065 |
rs748836145 | in-del | -/T | 0.117188 | 0.211804 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033787 | AAACTCCCTTTTATC[-/T]TTTTTTTTTTCAAGA | 8065 |
rs748836294 | snp | A/T | 1.77669e-05 | 0.00298046 | intron-variant | CUL5 | GRCh38.p7 | 11:108094785 | CATTGTTAATTTACT[A/T]TATATTCCTGATATT | 8065 |
rs748838865 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103915 | CTGCACCCATCAACC[C/T]GTCATCTACATGAGG | 8065 |
rs748859059 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038360 | GTCAATAACCTTTTA[C/T]TTGCTACAGTTAGTG | 8065 |
rs748863807 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026612 | TTTAAATTCACTAGC[A/G]GTTTCTCTCCCTTTC | 8065 |
rs748882850 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108073302 | TCCCCAGTTTTAAAT[G/T]AGTTTTATTAAAATT | 8065 |
rs748900558 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079060 | ATGAGTAGATAGATC[A/T]TCTTCTCTTTCACCC | 8065 |
rs748905633 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018727 | CTTAATGTGGCACCC[A/G]CACACATTTATTTTT | 8065 |
rs748925540 | snp | A/C | 1.68738e-05 | 0.00290458 | intron-variant | CUL5 | GRCh38.p7 | 11:108009389 | TAAGACCCTCACTCC[A/C]GCTTGGGTTTTACTG | 8065 |
rs748932601 | snp | A/G | 1.64887e-05 | 0.00287125 | missense | CUL5 | GRCh38.p7 | 11:108098479 | ACTACAGAAAGGATG[A/G]GAGAAGAAGAGAATG | 8065 |
rs748970769 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108074605 | AGGTCGGGAGTTCGA[C/G]ATCAGCCTGATCAAC | 8065 |
rs748993767 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027877 | ATTATTCTGTCTTTC[C/T]GACACACTTTATTTA | 8065 |
rs749068618 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090363 | GCGTGGTGGTGGGGG[G/T]CCTGTAGTCCCAGCT | 8065 |
rs749072904 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063145 | CCACTGCACCCGACT[A/C]TTCATTCTGGTTTTT | 8065 |
rs749118257 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009133 | TGAGGTCTTTCGCGT[G/T]GGGAAGCTCCGGTGA | 8065 |
rs749131779 | snp | C/T | 7.54546e-05 | 0.00614179 | intron-variant | CUL5 | GRCh38.p7 | 11:108046411 | TTGTTTTAAAACTAC[C/T]CAGATAATATCATAT | 8065 |
rs749132673 | snp | C/T | 1.81648e-05 | 0.00301365 | missense | CUL5 | GRCh38.p7 | 11:108094487 | GCTTTTAAGGAAATG[C/T]ACAAAAATAATAAAT | 8065 |
rs749166092 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088434 | ACTAGATTATTTAAC[A/G]TGAGAAATTCGCTTG | 8065 |
rs749200961 | in-del | -/AA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026990 | TGAGACTCCGTCTCA[-/AA]AAAAAAAAAAAAAAA | 8065 |
rs749202578 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065873 | AGCTTCTATTTGGCC[A/G]TCTTGCTCCACTCCT | 8065 |
rs749228387 | snp | A/G | 1.65787e-05 | 0.00287907 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108052734 | TAGTGCAATGAAGCT[A/G]GTACATGCTGAGAGA | 8065 |
rs749234937 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019757 | ATAAGTGACTGTGTT[A/T]CTGGTTTATGTATAT | 8065 |
rs749288062 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020827 | ATAATTTAGCATAGC[C/G]TAAGTGTTTATAAAG | 8065 |
rs749294769 | snp | A/G | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008127 | CACTAAGTAATATTT[A/G]ACTTGTGTAGCCATC | 8065 |
rs749323382 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024955 | TATTCCAACAGTCCA[C/T]CTCCACTACTAAAGC | 8065 |
rs749378239 | in-del | -/TTC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108097410 | GTGACCAATCCCAGT[-/TTC]TTGTCTTACTGTAAA | 8065 |
rs749378532 | in-del | -/TTTTTTTT | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007773 | TTTTTGTTTTTTTTG[-/TTTTTTTT]TTGAGACAAGAGTCT | 8065 |
rs749388881 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102983 | GTATTTTTTATAGAG[A/G]TGGGGTTTCGCCATG | 8065 |
rs749431513 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090104 | AAATGTTCTTAATAC[-/T]TTTCAGTAAAGTATC | 8065 |
rs749478836 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088847 | ATTTTTATTCTACAG[C/T]TTCTTGAAAGGAATA | 8065 |
rs749490860 | snp | C/T | 2.16097e-05 | 0.003287 | intron-variant | CUL5 | GRCh38.p7 | 11:108073509 | TAAGGTATATATTCC[C/T]ATATATATAAAAAAC | 8065 |
rs749506955 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043284 | TTGCCATGTGGCCTA[A/G]GCTAATCTCGAACTT | 8065 |
rs749538652 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043544 | TAAAGATCACTTTAG[C/T]TTCTTGTTTAATAGA | 8065 |
rs749572071 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093529 | CAGCATTATCACTTT[C/T]CATTTCCTGTTTACT | 8065 |
rs749578838 | snp | C/T | 3.82263e-05 | 0.00437169 | intron-variant | CUL5 | GRCh38.p7 | 11:108073376 | AAACTTAATGTAAAA[C/T]CTTTTGTTTCTAGGA | 8065 |
rs749589203 | snp | C/T | 1.65081e-05 | 0.00287293 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108097650 | GTCTTTAGTAGCTTT[C/T]CCAAAACTCAAACGG | 8065 |
rs749589442 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018118 | CAGAGAGGAATGGAG[A/G]AAGGGCATTTTTCTT | 8065 |
rs749617853 | snp | A/T | 3.70672e-05 | 0.00430491 | intron-variant | CUL5 | GRCh38.p7 | 11:108088689 | TGTATTTCAACTTTT[A/T]AAATTACCTTACTTT | 8065 |
rs749631587 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108094265 | GTATTAGACAATAAA[A/G]TTCTAATAAATGAGA | 8065 |
rs749728421 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082784 | GACTAAGGGCCATAC[C/T]ACCATGCCCGGCTAA | 8065 |
rs749732912 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108049639 | GAGCCACCACGCCTG[G/T]CCCATATATTGTTTA | 8065 |
rs749782694 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024044 | TCTTTGCAGTTTACT[C/T]TCTAAGCCTGATGAA | 8065 |
rs749782953 | snp | A/T | 1.65993e-05 | 0.00288086 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054761 | CACCCTCGTATTTAC[A/T]ACAAAATGGTGTACA | 8065 |
rs749813627 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096052 | AGTGAGCCAAGATTG[C/T]GCCACTACACTCCAG | 8065 |
rs749831018 | in-del | -/GTC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013562 | ACTAGCATGCCAGAG[-/GTC]GTCATCTCCCTAATA | 8065 |
rs749837293 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036642 | ACCACTGTGCCAGGC[C/T]AATTTTTGTATTTTC | 8065 |
rs749871317 | snp | A/C | 3.40234e-05 | 0.00412439 | intron-variant | CUL5 | GRCh38.p7 | 11:108072506 | ATATATATCAAGGCT[A/C]TTTTTTAAATGTAGG | 8065 |
rs749873198 | snp | A/G | 1.6836e-05 | 0.00290133 | intron-variant | CUL5 | GRCh38.p7 | 11:108097592 | TGATCTTAGTATTCC[A/G]TACTGTTTATAGATG | 8065 |
rs749873785 | in-del | -/AAAC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064719 | TGTCTCAAAAAACAA[-/AAAC]AAAACAAAACAAAAA | 8065 |
rs749890320 | snp | A/C | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032167 | ATGTACCCCAAACTT[A/C]AAAGTTAAAGAAAAT | 8065 |
rs749890524 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108046276 | TATTCACAGGGATGT[A/G]CATGCAGTCTGTCTT | 8065 |
rs750035078 | snp | C/T | 1.66891e-05 | 0.00288864 | intron-variant | CUL5 | GRCh38.p7 | 11:108033928 | TAAGTACCCCACTAA[C/T]TCTGTTTGCTAGCAT | 8065 |
rs750054306 | in-del | -/TT | 0.00444476 | 0.0469321 | intron-variant | CUL5 | GRCh38.p7 | 11:108098574 | TTAAAAAAACTTTAG[-/TT]TTTTTTTTTTTTTTT | 8065 |
rs750079166 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020456 | AGATTGAGAATAAAA[A/T]ACCTTTTTTTAATAG | 8065 |
rs750085506 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022298 | GTAAGTGAATTATTT[A/G]AAAATGATTCTATTG | 8065 |
rs750086852 | snp | C/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033203 | AGGACACATTTCTCT[C/G]CCGGCATCAATGTAT | 8065 |
rs750108708 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053944 | TCCACTTCCCAAGTT[C/G]AAGCAATTTTCATAC | 8065 |
rs750179997 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026023 | GGGAAAATCTGGTTC[A/C]TGTTATTCTGTCATG | 8065 |
rs750231324 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014251 | ATTAGGAGAAAATTT[A/G]GTAGGAATCTAGGCT | 8065 |
rs750232747 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072218 | AAACGAACAACTACT[C/G]CTAATGGCATTGTAT | 8065 |
rs750261739 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090023 | CCAGCCTGGGTAACA[A/G]AGTGGGACTCCATTT | 8065 |
rs750291454 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058928 | AGGCTTCCGAGCTGT[G/T]CTGCTGAACAGGCAT | 8065 |
rs750349574 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077492 | AAAATTAGCCAGGCA[C/T]GGTGGTGCGCACCTG | 8065 |
rs750387319 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087710 | CCCACGCGTATAATC[C/G]TAGCACTTTTTTGGG | 8065 |
rs750395634 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108091643 | GCATTGAACAGAGAT[C/T]TTACCACTGTACTCC | 8065 |
rs750409533 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108044395 | TGGCACATACCTGTG[G/T]TCCCAGCTAGTCGGG | 8065 |
rs750415043 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050952 | GTCCTCATTTTCCAT[A/G]TATCTTTCCACTTGT | 8065 |
rs750429217 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019123 | TATGGGAGGATGTGC[A/G]TGGGTAATAAGCAAA | 8065 |
rs750456951 | snp | A/G | 1.7348e-05 | 0.00294512 | intron-variant | CUL5 | GRCh38.p7 | 11:108009421 | GTGGCCGCCGGGTTC[A/G]GCTCTTTGGGAAAGG | 8065 |
rs750482292 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095734 | ACTGTATCCTCTCAT[G/T]TAGCAGGAAATATAT | 8065 |
rs750539161 | in-del | -/CAGA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098333 | TTAAATCTTTTCTCT[-/CAGA]CATTGTTGCTATAAT | 8065 |
rs750544241 | snp | C/G | 1.72142e-05 | 0.00293374 | intron-variant | CUL5 | GRCh38.p7 | 11:108072317 | TGATTACATGAATGT[C/G]TTCTCTCCTTCCAGA | 8065 |
rs750546519 | snp | A/G | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007058 | CTTCAAATTTTGTTA[A/G]CTATTTTCTCTTTGA | 8065 |
rs750606401 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036344 | GTCTCACTAACTCTT[C/G]CTGATTGGGACAATC | 8065 |
rs750694558 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024719 | TTTTGTACAACAGAT[A/G]CCACATTACAAAATT | 8065 |
rs750708971 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037636 | AGTGACAACACATAT[A/C]AAATATTGTCTACCA | 8065 |
rs750711197 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098571 | AGTTTAAAAAAACTT[C/T]AGTTTTTTTTTTTTT | 8065 |
rs750738840 | in-del | -/A | 2.10047e-05 | 0.00324066 | intron-variant | CUL5 | GRCh38.p7 | 11:108054625 | CATAATTGGAGTAAT[-/A]ACTTTATTTTCTGTT | 8065 |
rs750769865 | in-del | -/CTC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013451 | TTCCAGCTGGGTCTT[-/CTC]CTGATAACTAGTATT | 8065 |
rs750774740 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108078598 | AAATTTTCCTATTAC[C/T]GTTTTAAAAAATTGT | 8065 |
rs750844996 | snp | C/T | 1.66513e-05 | 0.00288537 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094411 | TGGTATGCCAGCGGA[C/T]TATGTAAACAAGCTT | 8065 |
rs750928280 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080262 | CCACCATACTTTACT[A/C]ATTTCTTTTAGAGAT | 8065 |
rs750946550 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108062407 | TTGTTTATCCATATC[A/G]TTGCTGATCTGAGTT | 8065 |
rs750950620 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076248 | TATGTTGCCCAGGCT[C/G]TTCTTGAACTCCTGG | 8065 |
rs750953276 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067842 | GTTATAGAATAAGAT[G/T]ACTCAGCAGTTGGGG | 8065 |
rs750978581 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017945 | TTTTGACTATTTTTT[C/G]TTGAATGTTCTTTTT | 8065 |
rs751000380 | snp | A/T | 1.64982e-05 | 0.00287208 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108046327 | AAAAATTCATCAGGC[A/T]TTAAAAGAAGATATT | 8065 |
rs751001359 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064362 | CCATCCTTGCATCCA[C/T]GGATAAATCCCACTT | 8065 |
rs751018085 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022020 | TATCCATCGATCCAT[A/C]CATTCTTAGAGATGG | 8065 |
rs751033486 | snp | C/T | 7.5933e-05 | 0.00616123 | intron-variant | CUL5 | GRCh38.p7 | 11:108094545 | TACATGTATATATTT[C/T]TTAAACTTAGAAGAA | 8065 |
rs751059201 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103370 | TTCAAGACCAACCTG[C/G]ACAACATAGCAAAAC | 8065 |
rs751087513 | snp | A/C | 1.68162e-05 | 0.00289962 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108073473 | TTTTCAAGATGATCC[A/C]CGATTTCTTACTGCA | 8065 |
rs751147046 | snp | A/C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084020 | CATCATCTGTCATTA[A/C/G]TGTTAGTGTATTTTA | 8065 |
rs751197386 | snp | C/T | 3.30115e-05 | 0.00406259 | synonymous-codon, intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108049958 | ATGGCGAAAGTTCTT[C/T]ACACAATGTGATATT | 8065 |
rs751222997 | snp | A/C | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108031851 | GCCATAAAAAAGAAC[A/C]AGATCATGTCCTTTG | 8065 |
rs751257159 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019489 | GCATATTGATGTTTT[C/G]GTCAACAACGGATCA | 8065 |
rs751291552 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036175 | TTCTTCCATCTGGAG[A/G]TTTCGTTTGTTTTCA | 8065 |
rs751320363 | in-del | -/CCT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071348 | TCACTGTAGCCTTGA[-/CCT]CCTGGGCTCAAGCGA | 8065 |
rs751341507 | snp | C/T | 1.66821e-05 | 0.00288804 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054707 | ACAATTTTGAGAAGG[C/T]ATACTTGGATTCAAC | 8065 |
rs751353763 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083333 | CATTAAGTAGTTTCC[A/G]ATGTGTTGCTATTAC | 8065 |
rs751412096 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069280 | GTCTCTTAAACAAAC[-/A]AAAAAAACCTTCCTT | 8065 |
rs751413508 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102635 | CCTCCCTGGCTGGTT[A/T]TCATATCTATATAGG | 8065 |
rs751521724 | snp | C/T | 1.70784e-05 | 0.00292214 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108095544 | GATAACATTTAAGAA[C/T]GAAGTTGGTCAATAT | 8065 |
rs751541133 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025856 | AGTGAAACCCCTAGC[A/G]GCTGTTTGGGTTTCC | 8065 |
rs751554360 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029741 | GAGTATTAGGGAAAC[A/G]TGTTTATTATGTGTT | 8065 |
rs751608745 | snp | A/G | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107376 | GGTGAAAGATTTGCT[A/G]GTTTTACAGAAAGAT | 8065 |
rs751625732 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053616 | ATGGTGTTCATAAGA[G/T]TAATGTTTAAGCACT | 8065 |
rs751647193 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016881 | CTCATGCCCAACACT[C/T]TGGAAAGCAGAGGCA | 8065 |
rs751647670 | snp | A/G | 1.66324e-05 | 0.00288374 | synonymous-codon, intron-variant | CUL5 | GRCh38.p7 | 11:108104255 | GCTGCAGACTGAATT[A/G]GTAGAAATTTTGAAA | 8065 |
rs751669135 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027036 | ACTTCCTCTCACCCT[A/G]TCAATTACCATGCCA | 8065 |
rs751727258 | snp | A/G | 1.64895e-05 | 0.00287132 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033888 | GGAATCTGTTACAAA[A/G]CAGCAGTGGTTTGAT | 8065 |
rs751734895 | in-del | -/TTTTTTTTTTTTTTTTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048654 | CTCCACCACCTTTTT[-/TTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 8065 |
rs751742251 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095451 | ACAGCAACCTTTTTC[A/G]TATATAAATTCATGT | 8065 |
rs751781080 | snp | A/G | 1.77366e-05 | 0.00297792 | intron-variant | CUL5 | GRCh38.p7 | 11:108052825 | TGAACTTTTATGATC[A/G]TAATTTCTGTTTCAT | 8065 |
rs751799211 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034915 | GAATTTTTAAAACTT[C/T]TCAAAATGGGCTTAT | 8065 |
rs751814219 | in-del | -/TAATC | 1.81342e-05 | 0.00301111 | intron-variant | CUL5 | GRCh38.p7 | 11:108094533 | TATTTTATAATTACA[-/TAATC]TGTATATATTTTTTA | 8065 |
rs751830239 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082174 | CCTTGGTATTTTCTT[C/T]GGATGCTGTTGTAAA | 8065 |
rs751830357 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024782 | CCATATATTTGCAAT[-/A]AAAAAAAAATAGTAG | 8065 |
rs751840064 | snp | C/G/T | 5.3599e-05 | 0.00517659 | intron-variant | CUL5 | GRCh38.p7 | 11:108088675 | GTACATGAATTTTTT[C/G/T]TATTTCAACTTTTAA | 8065 |
rs751851304 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100175 | GTGGTAGTGGTGGAA[A/C]TTGCCCTGCCAAATA | 8065 |
rs751864359 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108055536 | ACCTCACTGTAACTC[C/T]TGGGCATAAGGGCCC | 8065 |
rs751956994 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011716 | CACTGCAACTTCCGC[C/T]TCCCGGGTTCAAGCG | 8065 |
rs751985714 | in-del | -/CA | 1.73616e-05 | 0.00294627 | frameshift-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054954 | TAACTCCGTTGAAGC[-/CA]AGTAAGTAATTTTGT | 8065 |
rs752016413 | snp | G/T | 0.000207152 | 0.0101751 | intron-variant | CUL5 | GRCh38.p7 | 11:108098579 | AAAACTTTAGTTTTT[G/T]TTTTTTTTTTTTAAA | 8065 |
rs752018465 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013289 | CCCTTTTCTATCTTT[A/G]TATATTTTTTTCTGG | 8065 |
rs752037343 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085926 | AAGCACTGAATTGTA[C/T]ATTTTAAGTGAGTGA | 8065 |
rs752048456 | snp | C/G | | | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074496 | TACTGTGCCCAGACT[C/G]TTTTTGTCTATTTTA | 8065 |
rs752065447 | in-del | -/ATTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043457 | TTTAATCATTTTGTA[-/ATTT]ATTCTAAGAGTATTG | 8065 |
rs752090983 | snp | A/T | 1.75496e-05 | 0.00296217 | intron-variant | CUL5 | GRCh38.p7 | 11:108052628 | ATATTAATAATTGAA[A/T]ATTATGTTACAATTT | 8065 |
rs752098555 | snp | C/T | 2.03664e-05 | 0.00319105 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033762 | CTTTTTATTTAACTG[C/T]ATTTAAATTAAACTC | 8065 |
rs752111667 | snp | A/G | | | intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108061140 | TTTTTTCTTCACGGA[A/G]TCTAGCAAAAGGAGA | 8065 |
rs752116899 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075544 | TGACAGCAGGCTCTA[G/T]AAGTGACTTGTCAGG | 8065 |
rs752143531 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075306 | ATTCTGCAAGGAAAC[C/T]TATTTAAAACCCTGC | 8065 |
rs752181591 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101471 | CTTCCCTGCTCTCTT[C/T]CCCCTGCTCTTACTG | 8065 |
rs752207884 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024418 | ACAGAGCAAAATCTT[A/G]TCTCAAAAAATAATA | 8065 |
rs752216993 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012086 | GTTTTGTATCTCTGA[A/G]AACCTTTCCATGTAA | 8065 |
rs752267483 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087306 | TATGCATATATTTTA[C/T]GTATGTGTATGCACG | 8065 |
rs752269566 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102454 | GACTCAGCCCCCTGC[A/G]TAGCTGGGACCACAG | 8065 |
rs752272713 | snp | A/G | 1.80598e-05 | 0.00300493 | intron-variant | CUL5 | GRCh38.p7 | 11:108094767 | TTTATTTTGAATTTT[A/G]TCCATTGTTAATTTA | 8065 |
rs752305845 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057063 | AGGTGAAATTGTTCT[C/G]ATCTCCTACTGCAAT | 8065 |
rs752319979 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076391 | CTCTCTAGACTTTTT[C/G]CATCTTGTGTGTCTG | 8065 |
rs752367600 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029896 | ATTTTTAATTGCAGG[A/G]CTTACACTATATTTA | 8065 |
rs752380005 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083661 | ACGAGCATGATGGTG[C/T]GTGCCTGTAGTCCTA | 8065 |
rs752477055 | snp | A/G | 3.427e-05 | 0.00413931 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009304 | GGCCTGGCCGGGAGC[A/G]CCACGAATTCTCGCG | 8065 |
rs752477813 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033533 | TAAGTGTCCAGAGAT[C/T]ATCTACTAGAAGCCA | 8065 |
rs752546234 | snp | C/T | 1.66543e-05 | 0.00288563 | intron-variant | CUL5 | GRCh38.p7 | 11:108097619 | GATGCTAATTGTTTT[C/T]TCCTTATTCTTCATA | 8065 |
rs752569205 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034702 | ATGTCCTCCTCCTCC[A/G]CTGTCTCTTCCCAGC | 8065 |
rs752609578 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080543 | TGGGACTACAGGTGT[C/G]TGCCACCACGCCCAG | 8065 |
rs752625767 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042815 | TTGCCCAGGCTGGAG[G/T]GCAGAAGTGCAGTCT | 8065 |
rs752642592 | snp | C/T | 1.70194e-05 | 0.00291709 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108073485 | TCCACGATTTCTTAC[C/T]GCAAGAGATAAGGTA | 8065 |
rs752683039 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069386 | TTCTAGCCTTCTCTT[C/T]CACTGTCTGTTTCTT | 8065 |
rs752706904 | snp | A/C | 1.66015e-05 | 0.00288105 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054748 | TATAGAACACAAGCA[A/C]CCTCGTATTTACAAC | 8065 |
rs752715219 | snp | A/T | 1.6851e-05 | 0.00290263 | intron-variant | CUL5 | GRCh38.p7 | 11:108094347 | CCAGTAATATATCAG[A/T]TTATGTATTTATTAC | 8065 |
rs752740266 | snp | A/G | 3.31631e-05 | 0.00407191 | intron-variant | CUL5 | GRCh38.p7 | 11:108097763 | GTTTAATGTAAGCTC[A/G]TTAGTTGATCTAAAA | 8065 |
rs752754462 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027198 | GCTGGAGTGCAGTGG[C/T]GCCATCATGGCTCAC | 8065 |
rs752754781 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039946 | TGATTGTCCTACTAC[G/T]TGGAAACAAAATACA | 8065 |
rs752775671 | snp | C/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106311 | GTTTGTTGTTTTAAA[C/T]CATAATTGTTCTCAG | 8065 |
rs752792498 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075085 | AATATACTGAAGGGA[A/G]GAAGGAAGAAAGAAT | 8065 |
rs752805397 | snp | C/T | 3.3295e-05 | 0.00408 | missense | CUL5 | GRCh38.p7 | 11:108089568 | TGACACGACGTCTTA[C/T]ATTAGACATCTCTGC | 8065 |
rs752848268 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022581 | ATTTCTGGCTGATAA[C/T]ACTTACCCCCAGCCC | 8065 |
rs752880814 | in-del | -/GCCTGGG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108045831 | TGCCAGTGCACACTA[-/GCCTGGG]CAACATAGTGAGACC | 8065 |
rs752885515 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103142 | CTGGTACTGGAAAAG[A/G]TAAAAGAGAAAAGAA | 8065 |
rs752950898 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028604 | AGCACTTTCGGAGGC[C/T]GAAGCGGGCGGATCA | 8065 |
rs752984855 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050355 | GTATTTTATTTCTCT[A/G]TTCTTTCTTTGTACT | 8065 |
rs753023995 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020303 | GTTGTTACCATAGGA[A/G]ATGACAGCCCCATTC | 8065 |
rs753028117 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061923 | AGAGAGAGAATGTGC[A/G]GGAGAAACTGCCACT | 8065 |
rs753069112 | snp | A/G | 3.35768e-05 | 0.00409723 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108009366 | GGCGACGTCTAATCT[A/G]TTAAAGGTAAGACCC | 8065 |
rs753074759 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031419 | GTGCTGGTGTACTAG[A/C]AAGTTAGGTTTTACA | 8065 |
rs753080041 | in-del | -/TTG | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007052 | ATTAAACTTCAAATT[-/TTG]TTAACTATTTTCTCT | 8065 |
rs753116044 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086499 | ATCACTTTGATTGTT[-/A]ACAGTAGTTCACACC | 8065 |
rs753117966 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059446 | TGACCAGGGCACCGA[C/T]AGGGAGGGAGTGTAT | 8065 |
rs753138013 | snp | G/T | 1.67964e-05 | 0.00289792 | intron-variant | CUL5 | GRCh38.p7 | 11:108072486 | TTTTTCAATGGCAAT[G/T]ATAGATATATATCAA | 8065 |
rs753145173 | snp | A/T | 5.60187e-05 | 0.00529209 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033784 | ATTAAACTCCCTTTT[A/T]TCTTTTTTTTTTTCA | 8065 |
rs753162296 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066562 | ATCTTGCAAGGATTC[C/T]TTTAACTCACCTTGT | 8065 |
rs753170347 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085604 | TCTTAGTAAAAGATA[C/T]GTGTTAAAAAAGGAA | 8065 |
rs753171866 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099101 | CCTCAACTCCCTGGG[C/T]TCAAAGGATCCTCCC | 8065 |
rs753183115 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084744 | CTTTAATTAATTAAG[A/G]TTAATAGCTTAACCA | 8065 |
rs753217381 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053815 | TCCTGAGTAGCTGGG[A/G]CTGCAGGCATGCACC | 8065 |
rs753267289 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010202 | TTTGCCTTAAAAGTA[C/T]GGACAGAAATGGGGG | 8065 |
rs753273024 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072839 | ATGTGTTGATTACAA[A/G]TAAAAACATTAAATT | 8065 |
rs753275756 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038938 | TTCTTTCTCTATTGA[A/G]GTACTCTTGGTATTT | 8065 |
rs753289338 | in-del | -/TG | 1.68869e-05 | 0.00290571 | intron-variant | CUL5 | GRCh38.p7 | 11:108095721 | TTTTGTTTTTAAGAC[-/TG]TATCCTCTCATGTAG | 8065 |
rs753332383 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022431 | TTATATATCTGCTCC[G/T]TTACTCATGACCTAG | 8065 |
rs753362071 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101313 | ATGCAGTTATGACAG[C/T]GTCCTGGATTCTTGC | 8065 |
rs753384163 | in-del | -/TT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084659 | AGATAAATTAATGAC[-/TT]TTAACTAAAAGAAAA | 8065 |
rs753411259 | snp | A/G | 1.66704e-05 | 0.00288703 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108072342 | TCCAGAATTACATTT[A/G]ATGTTTTCATTGATG | 8065 |
rs753448632 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068085 | AGGCACCCACCATGC[C/T]CGGCTAATTTTTAGT | 8065 |
rs753454390 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086910 | TCCTAGTCAGATAGT[G/T]TCTACTTCTTTGCTT | 8065 |
rs753461902 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108055669 | AAGGGCTCTCTCTGT[G/T]GCCCAGGCTGGAGTG | 8065 |
rs753491064 | snp | A/C | 1.65364e-05 | 0.0028754 | missense | CUL5 | GRCh38.p7 | 11:108094931 | GTAGAAGAATTCTAC[A/C]AAAAAAATCATAGTG | 8065 |
rs753497734 | snp | A/G | 2.88089e-05 | 0.00379521 | intron-variant | CUL5 | GRCh38.p7 | 11:108095510 | GATTCTTTATTAAAA[A/G]TCTGTTTTATCTATT | 8065 |
rs753516104 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010700 | TTACTATAACTACTC[C/G]CCCTCTTTCTTTAAG | 8065 |
rs753586265 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011847 | TGGCTAGGATGGTCT[C/G]CATCTCTTGACCTCA | 8065 |
rs753594078 | in-del | -/GTTGC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042799 | ACAGAGTCTTGCCCT[-/GTTGC]CCAGGCTGGAGTGCA | 8065 |
rs753605744 | snp | A/C | 2.41929e-05 | 0.00347791 | intron-variant | CUL5 | GRCh38.p7 | 11:108098568 | TGAAGTTTAAAAAAA[A/C]TTTAGTTTTTTTTTT | 8065 |
rs753622706 | snp | C/T | 1.69186e-05 | 0.00290844 | intron-variant | CUL5 | GRCh38.p7 | 11:108088490 | AATTGCAAACATTAA[C/T]CATTTTTCCATCAAC | 8065 |
rs753631356 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015632 | AATTTCAAGGGTGTC[G/T]GTGTTGGTCATGGGT | 8065 |
rs753660515 | snp | A/G | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108106058 | CACTTTAAGGTAGCA[A/G]ATGTCAATTATTAGA | 8065 |
rs753684766 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108046521 | TATTAATGAAATGAT[C/T]GTCATTAGTTGGATT | 8065 |
rs753709657 | snp | A/T | 3.55309e-05 | 0.00421476 | intron-variant | CUL5 | GRCh38.p7 | 11:108078151 | TCAATATTAAAAATA[A/T]TTTATTCCAAATTAT | 8065 |
rs753725634 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066860 | CACATCTGTACATAT[G/T]AACCATACACATGTT | 8065 |
rs753772946 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066739 | GCCAGGACACAGCAC[A/T]GTCTTTATAGCTGTG | 8065 |
rs753814466 | snp | A/G | 1.71557e-05 | 0.00292875 | intron-variant | CUL5 | GRCh38.p7 | 11:108052640 | GAAAATTATGTTACA[A/G]TTTGTTCTTGTTTTC | 8065 |
rs753842184 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080420 | TTGGTTGTTTGAGAC[C/G]GGGCCTTGCTCTATC | 8065 |
rs753846093 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095269 | TTACACCTTTCATTA[A/G]GGACAACTTCTAGAA | 8065 |
rs753897966 | snp | A/G | 1.66175e-05 | 0.00288244 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054889 | GGCAGATGCTAAATT[A/G]AAAGAAGAAGAAAAA | 8065 |
rs753899457 | snp | C/T | 1.6625e-05 | 0.00288309 | intron-variant | CUL5 | GRCh38.p7 | 11:108070063 | GTGCTATACAGCTTA[C/T]AGTAGCCTTGACTAA | 8065 |
rs753910529 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037737 | GCACATACCAAAATT[C/T]GAGACTGGCAGAAGA | 8065 |
rs753935924 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100140 | AGAATGATTGAGAAA[C/G]TTAAAAAAATAAAAA | 8065 |
rs753954628 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084686 | AAAAATCATTTTAGA[A/G]GCGATCTCAGGTGAT | 8065 |
rs753998146 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108045768 | AGAAGGCTGAGGAGG[C/G]AGGATCGCCTCAACC | 8065 |
rs754057441 | snp | G/T | 1.67863e-05 | 0.00289704 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108009357 | AAAGAACATGGCGAC[G/T]TCTAATCTGTTAAAG | 8065 |
rs754058003 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014347 | TCCTTGGGATTGTTG[C/G]AGCATAGAAACCCAG | 8065 |
rs754059466 | snp | G/T | | | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074118 | GTTACTTCCCAAGTT[G/T]GAATGATTCTAAAAA | 8065 |
rs754070914 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103804 | TTTCAAAATCTCTAT[A/G]GTCAGATTTTTTTTA | 8065 |
rs754089587 | snp | C/T | 1.67424e-05 | 0.00289326 | intron-variant | CUL5 | GRCh38.p7 | 11:108098356 | GTTGCTATAATAGGA[C/T]TTTTAAAGTGTTTTT | 8065 |
rs754100412 | in-del | -/GGAGAG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061894 | TCTTATGTGGCAGCA[-/GGAGAG]AGAGAGAGAGAGAGA | 8065 |
rs754107717 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038777 | ACTGACAATAATTAA[A/G]ACCCTTGTAAATTTT | 8065 |
rs754125306 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059755 | TGGGCGTGGTGGCAC[A/G]CACCTGTAATCTCAG | 8065 |
rs754137319 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026882 | TATTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 8065 |
rs754202739 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056634 | GTTGACTTTTTTTTT[-/A]AAACAGGTGGGCCAC | 8065 |
rs754217728 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064384 | ATCCCACTTGGTCAT[G/T]ATGAATGATTTCTTT | 8065 |
rs754272460 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077269 | AGGAGGGTGTGATCC[A/G]CTGTTTTTAAATGCT | 8065 |
rs754304944 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108097512 | GTTATATTCATGGAA[G/T]TACCACACATTTTAA | 8065 |
rs754321245 | in-del | -/AAAAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040614 | GAGACTCCGTCTCAA[-/AAAAA]AAAAAAAAAAAAAAA | 8065 |
rs754327177 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019281 | GTAGTTTGATTCTTT[C/T]GGTTAGTGGGGATTG | 8065 |
rs754369275 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051200 | CAATATGGGAAATTT[C/G]TGCCAAGGGAAAAAA | 8065 |
rs754399411 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070371 | CTGCTAAGAGTATAT[-/A]AACTTAAATTTTAAG | 8065 |
rs754411539 | snp | A/G | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007119 | ATTTTTTATAGCGAT[A/G]GCTACTTTGCACAGG | 8065 |
rs754425457 | snp | C/T | 1.67464e-05 | 0.0028936 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108089581 | TATATTAGACATCTC[C/T]GCCGATAGTGAAATT | 8065 |
rs754431280 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079222 | AATTCTTCTGCCTCA[C/G]CCTCCCGAGTAGCTG | 8065 |
rs754460500 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014563 | GTTATTATATTTTCT[A/G]TATATTTATAATCTG | 8065 |
rs754509625 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108054254 | CTTGCAATCCACTTA[C/G]ACAACCTAGTCATAT | 8065 |
rs754602438 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010753 | TAACCCATCCCACTC[C/T]GCTTTTCTCTTTTAT | 8065 |
rs754621931 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081084 | TTGAGGTCAGGAGTT[C/T]AAGACCAGCCTGGCC | 8065 |
rs754638416 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028897 | TCTTCATCTCACTTA[C/T]AGTAGAAACCAAAGT | 8065 |
rs754673122 | snp | A/G | 1.65042e-05 | 0.0028726 | synonymous-codon, intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108049961 | GCGAAAGTTCTTTAC[A/G]CAATGTGATATTTTA | 8065 |
rs754707359 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086917 | CAGATAGTTTCTACT[A/T]CTTTGCTTTCAGCAC | 8065 |
rs754774875 | snp | G/T | 1.6773e-05 | 0.0028959 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108095550 | ATTTAAGAATGAAGT[G/T]GGTCAATATGATTTG | 8065 |
rs754810606 | snp | A/G | 1.68182e-05 | 0.00289979 | missense | CUL5 | GRCh38.p7 | 11:108073475 | TTCAAGATGATCCAC[A/G]ATTTCTTACTGCAAG | 8065 |
rs754822984 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079302 | ATGGAGACGGGGTTT[C/T]GCCATATTGGCCAGG | 8065 |
rs754825681 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108091962 | GGCAAAATAACAATA[C/T]TCCATGTCTACAAAA | 8065 |
rs754848221 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108046711 | ACTAATACCTCTTCT[C/T]AAGTTGACAGTAATT | 8065 |
rs754889136 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066927 | TAAGATCATTGAGGG[C/T]ATGAACCATGTTTAT | 8065 |
rs754896298 | snp | A/T | 1.66849e-05 | 0.00288828 | intron-variant | CUL5 | GRCh38.p7 | 11:108097616 | ATAGATGCTAATTGT[A/T]TTCTCCTTATTCTTC | 8065 |
rs754901618 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033337 | GGGATTTCAGTCTCC[A/G]TGTTGAGTGACCCCC | 8065 |
rs754910829 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080429 | TGAGACGGGGCCTTG[C/G]TCTATCTCCAGGCTG | 8065 |
rs754950193 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071955 | ACCAAGGCGAGAGGA[C/T]TGTGTGAGCCCCGAA | 8065 |
rs754953211 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066766 | TGTGGACAGAGCACA[A/G]TCTTTGTCCTTAAGT | 8065 |
rs754971644 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108073348 | TTTTTTTGTGTTATT[C/T]TTTTTCTTTTAAAAA | 8065 |
rs755060151 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072489 | TTCAATGGCAATGAT[A/C]GATATATATCAAGGC | 8065 |
rs755074685 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059033 | AAGAGGCAGAGTCTC[A/G]CTATGTTGCCCAGGC | 8065 |
rs755094226 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037981 | GCTGTACACATTGGG[C/T]TATTGTAATCGTTTT | 8065 |
rs755102887 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103874 | GCAGGTTTGTTACAT[C/G]GGTATACACGTGTCA | 8065 |
rs755123295 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026098 | TTCTCCGCCTTACCC[A/G]ACATAAATTCTCTTC | 8065 |
rs755176411 | snp | A/G | 5.00246e-05 | 0.00500098 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054708 | CAATTTTGAGAAGGC[A/G]TACTTGGATTCAACA | 8065 |
rs755176963 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108046010 | GTGACATTGGGAGAT[A/G]GAGACATGCTTTCAT | 8065 |
rs755193857 | snp | A/G/T | 3.57528e-05 | 0.00422792 | intron-variant | CUL5 | GRCh38.p7 | 11:108052830 | TTTTATGATCATAAT[A/G/T]TCTGTTTCATGGAAA | 8065 |
rs755195450 | snp | A/G | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108106107 | ATTAAACTAAAATTA[A/G]TACGTACAGTTTTCT | 8065 |
rs755302125 | in-del | -/AGAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089134 | TGGGCAAGTGTAGAC[-/AGAA]AGGCCGAGAGAGATG | 8065 |
rs755307232 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095968 | GGGCGTGGTGGTGGG[C/T]GCCTGTAATCCCAGC | 8065 |
rs755316490 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065451 | GCTTATAGTGCGAGG[C/T]TTGCTAGAACTCAAG | 8065 |
rs755321572 | in-del | -/AA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096329 | TGCAATCCCATCTCT[-/AA]AAAAAAAAAAAAAAA | 8065 |
rs755348989 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056822 | GGAAGAGAGAAACTT[C/T]TTAGAGGTGGAACAT | 8065 |
rs755373639 | in-del | -/AAATG | 1.74821e-05 | 0.00295647 | intron-variant | CUL5 | GRCh38.p7 | 11:108072294 | AACTCTTACTCTAGT[-/AAATG]AAATGATTACATGAA | 8065 |
rs755385256 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083406 | GAATCTTTATCTACA[A/G]GATAGAGTCCCAGAA | 8065 |
rs755388563 | snp | G/T | 1.6855e-05 | 0.00290297 | intron-variant | CUL5 | GRCh38.p7 | 11:108009386 | AGGTAAGACCCTCAC[G/T]CCAGCTTGGGTTTTA | 8065 |
rs755399602 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019319 | GGGTTTTAAAATCAC[A/G]TAACTGGGAGCAATA | 8065 |
rs755407863 | snp | C/T | 1.6713e-05 | 0.00289072 | intron-variant | CUL5 | GRCh38.p7 | 11:108088515 | ATCAACTGCTTTTAA[C/T]TTGTTTTTTAGGGTG | 8065 |
rs755412933 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051289 | TTTTTTGGCCATTCT[A/G]TTGGTTGTGGGAAGC | 8065 |
rs755420554 | snp | C/G | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007188 | TTCGCCTCCCAAAGT[C/G]CTGGGCTTACAGGAT | 8065 |
rs755423974 | snp | A/G | 1.6625e-05 | 0.00288309 | synonymous-codon, intron-variant | CUL5 | GRCh38.p7 | 11:108104258 | GCAGACTGAATTAGT[A/G]GAAATTTTGAAAAAC | 8065 |
rs755467929 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036664 | TGTATTTTCATTAGA[C/G]ACAGGTTTTCACCAT | 8065 |
rs755483689 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083730 | CTGCAGTGAGCTATG[A/T]TGGCACCACTGTACT | 8065 |
rs755513330 | snp | G/T | 0.000128299 | 0.00800831 | intron-variant | CUL5 | GRCh38.p7 | 11:108098580 | AAACTTTAGTTTTTT[G/T]TTTTTTTTTTTAAAT | 8065 |
rs755543436 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009166 | ATGTAGGGGAGAAGA[C/G]TGAGGAAGCTCCTGG | 8065 |
rs755557284 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098815 | TAGGAAACTTATTTA[A/G]AACCAAAAAAGTTCT | 8065 |
rs755574417 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079157 | CACCCAGGCTGGAGT[G/T]CAGTGGTACGACCTC | 8065 |
rs755590251 | snp | A/G | 2.00427e-05 | 0.00316559 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033769 | TTTAACTGCATTTAA[A/G]TTAAACTCCCTTTTA | 8065 |
rs755607886 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038375 | CTTGCTACAGTTAGT[A/G]GCCTCAACATGATGT | 8065 |
rs755626679 | in-del | -/T | 3.37089e-05 | 0.00410528 | utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108009339 | TCGCGAGAGTCCAAG[-/T]TTAAAGAACATGGCG | 8065 |
rs755644465 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066767 | GTGGACAGAGCACAA[A/T]CTTTGTCCTTAAGTT | 8065 |
rs755690119 | snp | C/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106763 | GTCTCTTCTCTCCAG[C/T]GTACACTTAAAATTG | 8065 |
rs755691416 | in-del | -/AT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108078090 | GAAATAAAAACTAAC[-/AT]ATTTTTATGTGTTTT | 8065 |
rs755698513 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009604 | AGAAAAGCCTGGCTG[A/G]GCGCTGGCGAGGAGC | 8065 |
rs755699409 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108054046 | AGACGGGGTTTTGCC[A/G]TAGTGGCCAGGCTGG | 8065 |
rs755768427 | snp | C/T | 1.64852e-05 | 0.00287094 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108070152 | AGAGACTATCTTAGC[C/T]GAGTGCCAAGGCATG | 8065 |
rs755822476 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010641 | TTAATATATCTATAA[C/T]GCTTAAAACAGTGCC | 8065 |
rs755852422 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103760 | TTTCTTTCAGCAGAG[A/C]AGCAGAGGTAATTTT | 8065 |
rs755858151 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058929 | GGCTTCCGAGCTGTG[C/T]TGCTGAACAGGCATG | 8065 |
rs755893189 | in-del | -/TTAG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039916 | TCGTGTTTCTTGGTC[-/TTAG]TTAGAAGCATGTGAT | 8065 |
rs755918192 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103450 | CATTTAATTGAGTCA[A/G]TATAAACTGAAGATA | 8065 |
rs755918278 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088151 | TAATATATTAATCAT[-/A]AAAAGTTTTAAATGT | 8065 |
rs755923396 | snp | C/T | 2.08648e-05 | 0.00322986 | intron-variant | CUL5 | GRCh38.p7 | 11:108073507 | GATAAGGTATATATT[C/T]CTATATATATAAAAA | 8065 |
rs755941344 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108049657 | CATATATTGTTTATC[C/T]GTATTTCAGCTAATG | 8065 |
rs755988951 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059694 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT | 8065 |
rs756005607 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108062923 | GGATCTCAGCTCACC[A/G]CAACCTCCGCCTCCT | 8065 |
rs756082886 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108044431 | GAGGCAGGGTTGAGC[C/T]CAGGAGGTTGAGGCT | 8065 |
rs756115807 | snp | C/T | 1.68843e-05 | 0.00290549 | intron-variant | CUL5 | GRCh38.p7 | 11:108046377 | CACAGGCAGTAAGTT[C/T]TACATGCTTATTTTA | 8065 |
rs756126431 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077544 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 8065 |
rs756170103 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108097150 | AGCCCCCCAAGTAGC[C/T]GGGACTACAGGTGCA | 8065 |
rs756190651 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083438 | TGAGGATTGCTGGGT[G/T]TCTCTTAGTTTTCTG | 8065 |
rs756213320 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095920 | AGCCAACATAGTGAA[A/G]CCCCATCTCTACTAA | 8065 |
rs756222332 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069555 | GTTTTTTTTTATTTT[A/G]TGTGTGTTTGTGTAT | 8065 |
rs756231516 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082286 | CTCTCTTTCTTTCTG[-/T]TTTTTTTTTTTTTAA | 8065 |
rs756239421 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071116 | ATACAGTTTTATATT[C/G]TAATCTCTAATATAG | 8065 |
rs756275499 | snp | A/T | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007091 | TAAATGCACATTTTT[A/T]AAAAATTTTATTATT | 8065 |
rs756290653 | snp | C/T | 1.71091e-05 | 0.00292476 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009305 | GCCTGGCCGGGAGCG[C/T]CACGAATTCTCGCGT | 8065 |
rs756296209 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026029 | ATCTGGTTCCTGTTA[C/T]TCTGTCATGATGGGA | 8065 |
rs756297575 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027628 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGGGCTCA | 8065 |
rs756312290 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024756 | CCTTTATAATCCCCA[A/G]TTAGTGAAATGCCAT | 8065 |
rs756378846 | snp | G/T | 3.32375e-05 | 0.00407647 | intron-variant | CUL5 | GRCh38.p7 | 11:108054861 | AAAATGATTGCTATT[G/T]TGCTTCTGGACAGGC | 8065 |
rs756404794 | snp | C/T | 1.65507e-05 | 0.00287664 | synonymous-codon, intron-variant | CUL5 | GRCh38.p7 | 11:108104330 | GTGGCTAATAGAGCA[C/T]AAATACATCAGAAGA | 8065 |
rs756436977 | snp | G/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107469 | TGAATTCTTCCAAGG[G/T]CATGTTTGTGAAATA | 8065 |
rs756475449 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108054434 | ATGCAAAAATAGTCT[A/G]TATTATCTGTATTAT | 8065 |
rs756509653 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029865 | TACCTGTCTACTCTG[A/G]TACTCTGCACCTTTT | 8065 |
rs756529566 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018100 | ACTTTGTCTCTGGAT[A/G]TGCAGAGAGGAATGG | 8065 |
rs756571260 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063104 | CCTGGCTCAGCCTCC[C/T]AAAGTGCTGGGATTA | 8065 |
rs756577761 | snp | A/G | 1.66713e-05 | 0.0028871 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108089572 | ACGACGTCTTATATT[A/G]GACATCTCTGCCGAT | 8065 |
rs756626386 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064374 | CCACGGATAAATCCC[A/C]CTTGGTCATGATGAA | 8065 |
rs756636420 | snp | A/G | 1.82523e-05 | 0.0030209 | intron-variant | CUL5 | GRCh38.p7 | 11:108088683 | ATTTTTTGTATTTCA[A/G]CTTTTAAAATTACCT | 8065 |
rs756650723 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095864 | ACTTTGGAAGGCCGA[A/G]GTGGGCAGATCACTT | 8065 |
rs756669235 | in-del | -/AATT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108097327 | GGCCTGAAGTTCCAA[-/AATT]AATTATTACCTATGG | 8065 |
rs756697650 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012436 | ATGTTCTTCTCTGTT[-/C]CATGCTACCTCCCAA | 8065 |
rs756737464 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060097 | AGCAACTAGGTCACA[A/G]GTTATAAATTATTAA | 8065 |
rs756742016 | in-del | -/T | 0.000269193 | 0.0115984 | intron-variant | CUL5 | GRCh38.p7 | 11:108097597 | TAGTATTCCATACTG[-/T]TTTATAGATGCTAAT | 8065 |
rs756747463 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064587 | AGGTGTCAGGTGCCC[A/G]TAATCCCAGCTACTC | 8065 |
rs756750140 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076589 | TTCCAGGCTTCCGTC[A/C]TATATATGTACCAGT | 8065 |
rs756754508 | snp | A/G | 1.65195e-05 | 0.00287393 | missense | CUL5 | GRCh38.p7 | 11:108094935 | AAGAATTCTACAAAA[A/G]AAATCATAGTGGTAG | 8065 |
rs756761695 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030937 | CCTCAGATGATTTTC[A/C]CGTAGGTTGTTGTCA | 8065 |
rs756809930 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087043 | TCATTAAAAATAAAT[C/T]TTAATATTAGATCAG | 8065 |
rs756812464 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042959 | GTAGAGATGGAGTTT[C/T]GCTATGTTGGCCAGG | 8065 |
rs756813069 | snp | C/T | 8.41928e-05 | 0.00648763 | intron-variant | CUL5 | GRCh38.p7 | 11:108072494 | TGGCAATGATAGATA[C/T]ATATCAAGGCTATTT | 8065 |
rs756830082 | in-del | -/AT | 1.68166e-05 | 0.00289966 | intron-variant | CUL5 | GRCh38.p7 | 11:108072491 | CAATGGCAATGATAG[-/AT]ATATATCAAGGCTAT | 8065 |
rs756842395 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065548 | TGTGTCAGCTGAGTT[C/T]ATCCTACTTTTGCTT | 8065 |
rs756887400 | snp | C/T | 1.69444e-05 | 0.00291066 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033790 | CTCCCTTTTATCTTT[C/T]TTTTTTTCAAGAATA | 8065 |
rs756937686 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101954 | AGGAGCCTGGTATCT[C/G]AATACCATCAAGGGT | 8065 |
rs756999073 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069514 | ATGAGGCCATTTTAA[C/T]TACCCTAGAAAAAAG | 8065 |
rs757062451 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012278 | TTTCATTTCCAGTTT[A/G]TTGTTCCACCCCAAA | 8065 |
rs757088571 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070657 | TGTTTTCTTAAAAAG[A/G]TGTGTTTTGAGAGGT | 8065 |
rs757107436 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084216 | ACAACTAGAAAATCA[C/G]GTAAATGTAAAAAAT | 8065 |
rs757128524 | snp | C/T | 0.000177431 | 0.00941721 | intron-variant | CUL5 | GRCh38.p7 | 11:108094786 | ATTGTTAATTTACTT[C/T]ATATTCCTGATATTC | 8065 |
rs757138844 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057295 | GACCTCCCAGAGTGC[C/T]AGGATTACAGGCACG | 8065 |
rs757191940 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041707 | GCGATTCTCCTGCCT[C/T]AGCCTCCCAAGTATC | 8065 |
rs757264042 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088444 | TTAACATGAGAAATT[C/T]GCTTGTGAATCATTG | 8065 |
rs757277213 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047265 | GAGGCTGCCGTGAGC[C/T]GTGATCATGCCATTG | 8065 |
rs757316407 | snp | C/T | 1.70734e-05 | 0.00292172 | intron-variant | CUL5 | GRCh38.p7 | 11:108052643 | AATTATGTTACAATT[C/T]GTTCTTGTTTTCCTA | 8065 |
rs757327709 | snp | A/G | 1.6492e-05 | 0.00287154 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108097677 | ACGGCAAGTTTTGTT[A/G]TATGAACCTCAAGTC | 8065 |
rs757350223 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042902 | GAGTACCTGGGACTA[-/C]CAGGAGCGCACCACC | 8065 |
rs757409363 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108049044 | GGATATGATTCAGTG[A/G]GTTGTAGTATATTTC | 8065 |
rs757432043 | snp | A/C/T | 6.68656e-05 | 0.0057818 | intron-variant | CUL5 | GRCh38.p7 | 11:108098569 | GAAGTTTAAAAAAAC[A/C/T]TTAGTTTTTTTTTTT | 8065 |
rs757432547 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034926 | ACTTTTCAAAATGGG[C/G]TTATGTTATCTCCCA | 8065 |
rs757441384 | snp | A/T | 3.34683e-05 | 0.0040906 | intron-variant | CUL5 | GRCh38.p7 | 11:108098367 | AGGATTTTTAAAGTG[A/T]TTTTCACCATAAAAT | 8065 |
rs757498215 | snp | C/T | 1.68272e-05 | 0.00290057 | intron-variant | CUL5 | GRCh38.p7 | 11:108078163 | ATATTTTATTCCAAA[C/T]TATTTTTTGCAGGCG | 8065 |
rs757517918 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027118 | TCTAGTTTTCTTCTT[A/C]TTTATTTTTGTTTTT | 8065 |
rs757583690 | snp | C/G | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108106111 | AACTAAAATTAATAC[C/G]TACAGTTTTCTCTAA | 8065 |
rs757604814 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108055623 | CTAATAAATATATAT[A/G]TATATATACTTTATC | 8065 |
rs757607474 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040256 | AGGCCGAGGCTGGAG[A/G]ATTGCTTGAGGCCAG | 8065 |
rs757683581 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027642 | TCGAACTCCTGGGCT[C/G]AAGTGACCCGCCCGC | 8065 |
rs757736723 | snp | C/T | 1.6686e-05 | 0.00288838 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054914 | GAAAAACGAGCACTA[C/T]GTTATTTAGAAACAA | 8065 |
rs757790820 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075393 | GCATAGGCAACACAT[A/G]TTTCTGCAGTTTTAG | 8065 |
rs757828817 | snp | A/G | 1.67139e-05 | 0.00289079 | intron-variant | CUL5 | GRCh38.p7 | 11:108094387 | CTTTGGTTTATATTT[A/G]TAGGAAGTTGGTATG | 8065 |
rs757829304 | snp | G/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107389 | CTAGTTTTACAGAAA[G/T]ATTTGCTATCTTAAA | 8065 |
rs757833808 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051053 | CTGTGATGGTTACAG[C/T]AAAACACTCAGGCAT | 8065 |
rs757841984 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016915 | GGATCATTTGAGGCC[A/T]GGAGTTGGAGACTAG | 8065 |
rs757845508 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083845 | GTAGAATAGGTGGTG[C/T]GGCTATTGGAGGTGT | 8065 |
rs757888568 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087363 | ATACTTAAAATTTGG[A/G]TAGCTCAATCCTTGG | 8065 |
rs757888772 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102465 | CTGCGTAGCTGGGAC[A/C]ACAGGCGCGTGCCAC | 8065 |
rs757895585 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041623 | TAGACAAAGTTTTGC[C/T]CTTGTTGCCTAGGCT | 8065 |
rs757903012 | snp | C/T | 1.71079e-05 | 0.00292466 | intron-variant | CUL5 | GRCh38.p7 | 11:108072512 | ATCAAGGCTATTTTT[C/T]AAATGTAGGATTATT | 8065 |
rs757907999 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012974 | TGGAAAAGCAGCCCC[C/T]ATTTGCTGCCTTTAT | 8065 |
rs757936610 | snp | A/G | 1.65015e-05 | 0.00287237 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108046298 | GTCTGTCTTTGGGAT[A/G]ATAAAGGCCCAGCAA | 8065 |
rs757974663 | in-del | -/GT/T/TT | 0.328739 | 0.23909 | intron-variant | CUL5 | GRCh38.p7 | 11:108098573 | TTAAAAAAACTTTAG[-/GT/T/TT]TTTTTTTTTTTTTTT | 8065 |
rs758026102 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016630 | TGCCTCCTGCCTTGG[A/T]TAGTAGGTGGAGGAA | 8065 |
rs758039588 | in-del | -/CTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012523 | GTATGTCCCCTCTTA[-/CTT]TTTTTTTTTTTTTTT | 8065 |
rs758056190 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030719 | CTTTTAGGATGAACT[A/G]TGTTCGTGAATATAA | 8065 |
rs758061308 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069013 | CTGTAATCCCACACT[G/T]TGGGAGACTGACAGG | 8065 |
rs758062341 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018152 | TTGGTTTGGGAGGCC[G/T]GAGGTGGCATTGGAG | 8065 |
rs758121279 | snp | C/G/T | 1.67038e-05 | 0.00288992 | intron-variant | CUL5 | GRCh38.p7 | 11:108033930 | AGTACCCCACTAATT[C/G/T]TGTTTGCTAGCATAA | 8065 |
rs758123117 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076508 | TATTTGAATTTTTTT[C/T]AGGTTCTACCTATAA | 8065 |
rs758165587 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022546 | TGATATGTTCTAGAA[A/G]GATCTATGTAACATC | 8065 |
rs758174990 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048912 | CCTCGTGATCTGCCC[A/G]CCTTAGCCTCCCAAA | 8065 |
rs758204829 | snp | A/T | 1.76986e-05 | 0.00297473 | intron-variant | CUL5 | GRCh38.p7 | 11:108052823 | TCTGAACTTTTATGA[A/T]CATAATTTCTGTTTC | 8065 |
rs758225881 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034764 | TCAGTGTATCCCTTT[C/T]AGTAATGAAAATTTC | 8065 |
rs758260843 | snp | C/T | 4.71787e-05 | 0.00485666 | intron-variant | CUL5 | GRCh38.p7 | 11:108095521 | AAAAATCTGTTTTAT[C/T]TATTATAGATAACAT | 8065 |
rs758276900 | snp | C/G | 1.65195e-05 | 0.00287393 | missense | CUL5 | GRCh38.p7 | 11:108072364 | TCATTGATGGACAAA[C/G]TTCCTAATGGTATAG | 8065 |
rs758277363 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081892 | AGCTTTAAAAGCAAG[A/G]TGTGTGCATGTTTCA | 8065 |
rs758295121 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108055855 | AGGCTGATCTTGAAC[A/G]CCTAAGCTCAGGTGA | 8065 |
rs758303121 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023635 | GTGAATTGCTTGAGG[A/G]CTTTTCATTTATGTG | 8065 |
rs758334635 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069747 | GGTTTGTTGAATGAA[-/T]TGTATTCACACTTCT | 8065 |
rs758370885 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101493 | CTCTTACTGAGCTCT[G/T]GAAGCCTCTGAGACT | 8065 |
rs758388265 | in-del | -/ATA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063590 | TTTAATGTTAATTTT[-/ATA]ATAATAATAAAATTT | 8065 |
rs758431874 | snp | A/G | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107279 | AGAAAATATGACCTG[A/G]GTAGTTAAAAAGTAT | 8065 |
rs758439128 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059974 | GCACTGTGCCTGGCA[A/T]GATAGCTTTTACTGT | 8065 |
rs758454936 | in-del | -/TC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028667 | CATGGTGAAACCCCG[-/TC]TCTACTAAAATACAA | 8065 |
rs758465360 | snp | G/T | 2.78369e-05 | 0.00373064 | intron-variant | CUL5 | GRCh38.p7 | 11:108098577 | AAAAAACTTTAGTTT[G/T]TTTTTTTTTTTTTTA | 8065 |
rs758494147 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060844 | AAAAAAAAAAAGAAT[A/G]AGAATCTACCATGTC | 8065 |
rs758503745 | snp | A/G | | | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074337 | GTAGCTGGGATTACA[A/G]GGACCAACCACCATG | 8065 |
rs758534504 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092180 | ACTTTATTCCCACTA[G/T]GGTAGCTAAAATAAA | 8065 |
rs758549234 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047059 | ACAGTAGCTCAGGCC[C/T]GTAATCCCAGCACTT | 8065 |
rs758553158 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108046634 | ATATTTTTTGGGAGT[-/C]CCCACCACCATTATT | 8065 |
rs758590866 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093226 | ACTTGACAGAGTAAG[C/T]ATCTTTTCTTTGCCT | 8065 |
rs758592760 | snp | A/G | 3.36995e-05 | 0.00410471 | intron-variant | CUL5 | GRCh38.p7 | 11:108088500 | ATTAATCATTTTTCC[A/G]TCAACTGCTTTTAAT | 8065 |
rs758607583 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022682 | TCTGTAATCCACCCT[C/T]CCTCCTTGGTCTGGG | 8065 |
rs758622479 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015722 | AATGGTAGAATCTTT[C/T]ATGTTCTATGAAAAT | 8065 |
rs758738121 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031566 | GTCCTTTCTCTTTTG[C/T]TTTTGTCAGGTTTGT | 8065 |
rs758739109 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079484 | AATATGTTATCTCCT[C/T]ATATACATTCGTCAG | 8065 |
rs758786272 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052367 | TCACCCAGGCTGGAG[A/G]GCAGTGGCGTGGTCT | 8065 |
rs758788901 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038942 | TTCTCTATTGAAGTA[C/T]TCTTGGTATTTTGGG | 8065 |
rs758804397 | in-del | -/A | 1.66181e-05 | 0.00288249 | intron-variant | CUL5 | GRCh38.p7 | 11:108054801 | AAATATGTAAGTTAG[-/A]AACTTAGTATATGTG | 8065 |
rs758810053 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061963 | ATCAGATTTTGAGAA[A/T]TCCCTGTCACAAGAA | 8065 |
rs758843544 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038029 | AATATTCTAATTTCC[A/G]AAATGATGTAGGACC | 8065 |
rs758866743 | snp | A/C | 5.11025e-05 | 0.00505457 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009321 | CACGAATTCTCGCGT[A/C]GTCTCGCGAGAGTCC | 8065 |
rs758881143 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072875 | AAATACAGAATTGAA[A/C]ATTGAAAATAGTAAT | 8065 |
rs758886905 | snp | A/G | 1.681e-05 | 0.00289909 | intron-variant | CUL5 | GRCh38.p7 | 11:108009376 | AATCTGTTAAAGGTA[A/G]GACCCTCACTCCAGC | 8065 |
rs758957771 | snp | G/T | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007053 | TTAAACTTCAAATTT[G/T]GTTAACTATTTTCTC | 8065 |
rs758958167 | snp | A/G | 3.38112e-05 | 0.0041115 | intron-variant | CUL5 | GRCh38.p7 | 11:108098554 | GTTGACAGAATGTCT[A/G]AAGTTTAAAAAAACT | 8065 |
rs759009868 | snp | A/G | 1.64846e-05 | 0.0028709 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108070137 | GGTGACATCATTTAA[A/G]GAGACTATCTTAGCT | 8065 |
rs759015562 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099793 | GTTCTGCCAGTTCTA[C/G]GTTTTCATATAAATG | 8065 |
rs759026347 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085650 | TGCTGTGACACATGG[A/C]TGAATCTTGAAAACT | 8065 |
rs759074668 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070460 | CTCAAAAGCAAGACA[C/G]TGCTTTTAAAGGCCA | 8065 |
rs759077221 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042808 | TGCCCTGTTGCCCAG[C/G]CTGGAGTGCAGAAGT | 8065 |
rs759132703 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082984 | CTCAGTTTATTTATT[A/G]GCTCAGATACCTTTT | 8065 |
rs759139516 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069266 | GCAGAGCAAGACTCT[C/G]TCTCTTAAACAAACA | 8065 |
rs759147113 | snp | A/G | 1.74857e-05 | 0.00295678 | intron-variant | CUL5 | GRCh38.p7 | 11:108050116 | CTTCAGAAAGAGGGT[A/G]ATTTGGAAGCATTTG | 8065 |
rs759149574 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035817 | GCTTTTGGTTCAGCA[C/T]AGCTTGTGTTGAGGT | 8065 |
rs759158703 | snp | C/T | 1.66297e-05 | 0.0028835 | intron-variant | CUL5 | GRCh38.p7 | 11:108078264 | TTTAAAACCATACTT[C/T]AAAAATACTTAAATT | 8065 |
rs759171901 | in-del | -/ATGAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067474 | TGAAACAAAAGTCTT[-/ATGAA]ATGAAATAATATTCA | 8065 |
rs759190936 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056829 | AGAAACTTCTTAGAG[A/G]TGGAACATTGTATCA | 8065 |
rs759279994 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026754 | CCAGCACTTTGGGAG[C/G]CTGAGGTGGGCGGAT | 8065 |
rs759289020 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025485 | TTACCTTTAAGTTTC[A/G]TTAGAGTGTGTCCAG | 8065 |
rs759298579 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075138 | TAATTCAATTAAGTG[A/G]TGATGGAGGCTTGTC | 8065 |
rs759436599 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016581 | AATATTTTGCTTAGT[C/G]TCCTGGTGAACCCAG | 8065 |
rs759447400 | snp | G/T | 8.60993e-05 | 0.00656066 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009298 | GGTCAAGGCCTGGCC[G/T]GGAGCGCCACGAATT | 8065 |
rs759452814 | snp | C/T | 1.65638e-05 | 0.00287778 | intron-variant | CUL5 | GRCh38.p7 | 11:108097760 | TCAGTTTAATGTAAG[C/T]TCGTTAGTTGATCTA | 8065 |
rs759487837 | snp | A/G | 3.37143e-05 | 0.00410561 | utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108009338 | TCTCGCGAGAGTCCA[A/G]GTTAAAGAACATGGC | 8065 |
rs759495447 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095036 | CAGTTTGGATGAAAG[G/T]AGCAGGACTCCGCAG | 8065 |
rs759530624 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050213 | AGATTTTATTGAATA[A/G]TATTCTTTTTTGTCT | 8065 |
rs759577436 | snp | C/T | 1.89568e-05 | 0.00307864 | intron-variant | CUL5 | GRCh38.p7 | 11:108054992 | CATTTTATGGGATTA[C/T]TTGAAATACGGAAGC | 8065 |
rs759667537 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100755 | TTGAAATGTGGCCAG[A/G]CGCGGTGGCTCACGC | 8065 |
rs759703831 | snp | C/T | 5.05114e-05 | 0.00502525 | intron-variant | CUL5 | GRCh38.p7 | 11:108046226 | ATGTTTTGTTCAGTT[C/T]TTGTTTCATTATTAA | 8065 |
rs759715482 | snp | A/C | 1.65666e-05 | 0.00287802 | intron-variant | CUL5 | GRCh38.p7 | 11:108089675 | CATTACATCATTTAT[A/C]TGTGTGCTTAAGTAA | 8065 |
rs759729399 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038797 | TTGTAAATTTTAGCC[A/G]TATTTTGGCCATGTT | 8065 |
rs759746075 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011269 | TTTGGTCTATATTAG[C/T]TAAGTACTTACCTGT | 8065 |
rs759758991 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086457 | TGATAGCTGTCCTCT[C/T]GATAGGTTGAATGAA | 8065 |
rs759791869 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108074666 | GAAAAATTAGCTGGA[C/T]GTGGTGGTACATGCG | 8065 |
rs759798315 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020592 | TCACCACGTTGCCCA[A/G]GCTGGTCTCAAACTC | 8065 |
rs759805272 | snp | A/G | 1.6543e-05 | 0.00287597 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108089512 | GGTACTTAAGTATGT[A/G]CAGAACAAAGATGTT | 8065 |
rs759828115 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010396 | CATGTCTTCTTTAGA[-/C]CACTGATATTTGATT | 8065 |
rs759854702 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086169 | TTTAAGATTTAAGGG[A/T]GTCTGTGAATCCCAA | 8065 |
rs759882560 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031744 | TCACAGCACTGTTCA[C/T]TCTAACAAAGACGTG | 8065 |
rs759921410 | snp | A/G | 1.68476e-05 | 0.00290233 | missense | CUL5 | GRCh38.p7 | 11:108073420 | GTTGAGCAGTTACTT[A/G]CACTATTTAATAGAT | 8065 |
rs759932639 | snp | C/T | 3.10882e-05 | 0.00394248 | intron-variant | CUL5 | GRCh38.p7 | 11:108095501 | TCATCATGAGATTCT[C/T]TATTAAAAATCTGTT | 8065 |
rs759946634 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067382 | AATTTAGCTCTCCTT[-/A]TTAATCCTCGTTGTA | 8065 |
rs759961340 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108078504 | CCTCATTAGTCACTA[A/C]AAGTATTCTATTACC | 8065 |
rs760001154 | snp | C/T | 1.65751e-05 | 0.00287876 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108095686 | GAACTTAGGAGGACT[C/T]TATGGGTTGGTTTAT | 8065 |
rs760006143 | in-del | -/AGT | 1.70748e-05 | 0.00292183 | intron-variant | CUL5 | GRCh38.p7 | 11:108095034 | TTCAGTTTGGATGAA[-/AGT]AGCAGGACTCCGCAG | 8065 |
rs760018698 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066451 | CCAGCAAGAGTCACT[C/G]TACTCCAATAAGAAA | 8065 |
rs760069504 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032724 | TGTTTGATTTGATAA[C/T]ATTTATTTAGATTTT | 8065 |
rs760082217 | snp | A/G | 1.64904e-05 | 0.00287139 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033890 | AATCTGTTACAAAAC[A/G]GCAGTGGTTTGATCT | 8065 |
rs760170220 | snp | C/G | 5.0347e-05 | 0.00501707 | intron-variant | CUL5 | GRCh38.p7 | 11:108072482 | GTTTTTTTTCAATGG[C/G]AATGATAGATATATA | 8065 |
rs760201649 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081743 | GGTGAGAGTGCGAGT[C/T]TCCGTCTCAAGAAAA | 8065 |
rs760225541 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066387 | ATACCCCTGATTTTT[A/C]AGACCCTTCATAATT | 8065 |
rs760227136 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092779 | CAGTTCTGTAGATAT[A/G]CTAAACTTCATTACA | 8065 |
rs760239169 | snp | G/T | 1.74759e-05 | 0.00295595 | intron-variant | CUL5 | GRCh38.p7 | 11:108052631 | TTAATAATTGAAAAT[G/T]ATGTTACAATTTGTT | 8065 |
rs760243551 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080309 | GCTCAGGCTGGTGTC[A/G]AACTCCTGGCCTCAA | 8065 |
rs760315187 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095208 | TTCAACATGATCCCA[A/G]CTATCTCAGTATTCC | 8065 |
rs760382968 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034389 | AAATCAGTGTAAACC[A/C]TATTGTTTATATAAA | 8065 |
rs760419619 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068359 | AGTCTTGCTCTGTCG[C/T]CCAGACTACACTGCA | 8065 |
rs760426901 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085431 | GGATGGGGAAGGGGG[A/G]GATGGGAAGTTACTG | 8065 |
rs760442421 | in-del | -/TTAG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011305 | CTATTTTGGTTCATA[-/TTAG]TTAAGTACTTACCTG | 8065 |
rs760477260 | in-del | -/TTC | 3.36766e-05 | 0.00410331 | intron-variant | CUL5 | GRCh38.p7 | 11:108046224 | AGATGTTTTGTTCAG[-/TTC]TTGTTTCATTATTAA | 8065 |
rs760477694 | snp | A/G | 1.68168e-05 | 0.00289967 | utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108009345 | AGAGTCCAAGTTAAA[A/G]AACATGGCGACGTCT | 8065 |
rs760484703 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072225 | CAACTACTCCTAATG[A/G]CATTGTATCCACAGA | 8065 |
rs760491860 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060691 | AAATACAAAAAATTA[C/T]CCGGGCATGGTGGTG | 8065 |
rs760518757 | snp | A/G | | | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074092 | TTTTTTCTCTTCTTT[A/G]ACTACCTTTCGTTAC | 8065 |
rs760518830 | in-del | -/TTCG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098055 | TTTGTGTTGTTTTGT[-/TTCG]TTTTTGTTTTTGTTT | 8065 |
rs760552994 | in-del | -/AGAGA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061507 | AATATTTACACAAGT[-/AGAGA]AAATACTATAATGAA | 8065 |
rs760605724 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012746 | GGATTACAGGCACAC[A/G]CCACCACACCCAGCT | 8065 |
rs760610126 | in-del | -/TGAACAGGA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067649 | AATTTCAACTACCAC[-/TGAACAGGA]TAATGTTCAAGTGAA | 8065 |
rs760618972 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108055075 | TTAATTGATTTTAGT[G/T]CTTTTTGCCTATGAG | 8065 |
rs760642230 | snp | A/G | 1.69502e-05 | 0.00291115 | intron-variant | CUL5 | GRCh38.p7 | 11:108088482 | AAAAAAATAATTGCA[A/G]ACATTAATCATTTTT | 8065 |
rs760644809 | snp | A/G/T | 9.95395e-05 | 0.00705414 | synonymous-codon, missense | CUL5 | GRCh38.p7 | 11:108078223 | ATTTAAACTTGAATT[A/G/T]CCTTTGAAGCAGAAG | 8065 |
rs760657137 | snp | C/G | 1.68015e-05 | 0.00289836 | intron-variant | CUL5 | GRCh38.p7 | 11:108094365 | ATGTATTTATTACCT[C/G]TTCCTTCTTTGGTTT | 8065 |
rs760671450 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098305 | TAAACAGTTCTGATA[C/T]TTTAGCATATTTTTA | 8065 |
rs760721831 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019982 | AGGCTCTTTTTAACA[A/G]CCAACTCTCAGGGAA | 8065 |
rs760761479 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060788 | GTTGCAGTGAGATCG[C/T]GCCATTGCACTCCAG | 8065 |
rs760785363 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031260 | AATCTCAGCTACTCG[G/T]AGGCTGAGGCATGAA | 8065 |
rs760828312 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065301 | GTGCTGGGATTACAG[A/G]CATGAGCCACTGCAC | 8065 |
rs760837528 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084628 | ATTCAGTACAACATT[A/G]CTAGTCCTATGAAGA | 8065 |
rs760849513 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085754 | TCAGCACATCCATAG[A/G]GTAGACTAGATGTTG | 8065 |
rs760869951 | in-del | -/AC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061558 | AGTCTTCCAGATTCA[-/AC]AGTTATCATTATTTT | 8065 |
rs760879716 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052141 | TAGCAAATTTTTGTA[C/T]TTTTTGTTGTTGTTG | 8065 |
rs760930219 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058699 | AGACCTGAATGATAG[C/G]GAACTAGCCTTGTGA | 8065 |
rs760963685 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038578 | TACTTGGGAGGCTGA[A/G]GCAGGATAATCACTT | 8065 |
rs760981487 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009986 | TACAGGACACAACCA[G/T]ATGACAACTGATGAA | 8065 |
rs761030056 | in-del | -/AAAAAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040613 | TGAGACTCCGTCTCA[-/AAAAAA]AAAAAAAAAAAAAAA | 8065 |
rs761057500 | snp | A/C | 1.6604e-05 | 0.00288127 | missense, intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108049902 | CAGCGAGTACTGAGC[A/C]ATCAAGATGATACGG | 8065 |
rs761066312 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013835 | GCACTTTGGGAGGAT[C/G]AGGTGAGAGGATTAC | 8065 |
rs761107973 | snp | C/T | 0.000167342 | 0.00914564 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108073437 | ACTATTTAATAGATT[C/T]AGTAAACTCGTCAAA | 8065 |
rs761111982 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089342 | GTATCAGGACTGGGT[A/G]TTTCTCAGAGATGGA | 8065 |
rs761112722 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108049830 | ATTTTGGCATGAATA[C/T]GTTCTTAATTTTTCA | 8065 |
rs761119758 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030577 | GGGAGGCGGAGGTTG[C/T]GGTGAGCTGAGATCG | 8065 |
rs761159529 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108091239 | GTATTTTTAGTAGAG[A/G]CACGGTTTTGCATGT | 8065 |
rs761167127 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042681 | TCACTCACCCTTACC[C/T]TGTCCTTGAGTTCCT | 8065 |
rs761237180 | snp | C/G | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106942 | TAGTTTAAAGACAGA[C/G]ACATCCCATCTGGAA | 8065 |
rs761306176 | snp | A/G | 5.0314e-05 | 0.00501543 | intron-variant | CUL5 | GRCh38.p7 | 11:108046237 | AGTTCTTGTTTCATT[A/G]TTAATGTTTGTTTAC | 8065 |
rs761325182 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092706 | GACTGTAAATAGTAT[A/G]GGGTTTCTTTTTGGG | 8065 |
rs761328484 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014994 | ACCTCCACCTCCTGG[A/G]TTCAAGCAATTCTCC | 8065 |
rs761355633 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064569 | TACAAAAATTAGCGG[A/G]CGAGGTGTCAGGTGC | 8065 |
rs761363321 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108073738 | TTCTCATTTTTCCAA[G/T]AATGTTTTTCTGTTT | 8065 |
rs761366260 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016388 | TCCTCCCACCTCATC[C/T]TCCCACAGGTGCAAC | 8065 |
rs761392143 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108091480 | CAGATGGCTTGTGCT[C/G]AGAGTTTGAGATGAG | 8065 |
rs761449232 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022245 | GGGTGTTTTCGGGGC[A/G]AACCAGTAGGTCAAC | 8065 |
rs761450817 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043979 | AGTGAGCCAAGGTGG[C/T]GCCATTGCACTTCAG | 8065 |
rs761450966 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060506 | TAAACGAAATTTGAG[C/T]GAGGTAGAAATAATT | 8065 |
rs761495057 | snp | A/C | 3.36378e-05 | 0.00410094 | synonymous-codon, intron-variant | CUL5 | GRCh38.p7 | 11:108104217 | CAAATAATGAAAATG[A/C]GAAAGAAAATTAGTA | 8065 |
rs761501776 | snp | C/T | 2.80116e-05 | 0.00374233 | intron-variant | CUL5 | GRCh38.p7 | 11:108095512 | TTCTTTATTAAAAAT[C/T]TGTTTTATCTATTAT | 8065 |
rs761525435 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084252 | TTTCATGTTATTTAA[G/T]AGCTATAGAAACAGC | 8065 |
rs761584657 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053234 | CGCTTCATCCTCCTC[C/T]TGGAGGCCTTTCTTA | 8065 |
rs761615310 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072200 | AAAAAAACAACAACA[A/G]AAAAACGAACAACTA | 8065 |
rs761644312 | snp | C/G | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008302 | ATCCCTCTTCTCTTA[C/G]TCCAGAGCTCTTACT | 8065 |
rs761648980 | in-del | -/TTTAT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102021 | TTTTATTTATTTTTG[-/TTTAT]TTTATTTTATTTTAT | 8065 |
rs761663521 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037415 | AATCCCAAGGTCACC[C/T]CTAGGCTCAGTGATT | 8065 |
rs761665872 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083375 | CAGAGGATAATATTG[G/T]ACATTGAATATTTGT | 8065 |
rs761668821 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009442 | TTGGGAAAGGCACGG[C/T]TCAGGTTCAGCTGCG | 8065 |
rs761685122 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014122 | TCACAGATTGAGGAA[A/G]TAATTTCTGGTGGGA | 8065 |
rs761701019 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103387 | CAACATAGCAAAACC[G/T]TGTGTCTGTATTTAA | 8065 |
rs761755622 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076876 | GGATATGTTCACTGC[A/G]ATAGGGAAGACTGTA | 8065 |
rs761769586 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020125 | ACAACATTGGGGATC[-/A]AATTTCAACATGAGG | 8065 |
rs761771885 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026671 | AATGTTCCTGTCAGC[A/G]TACAATCATACTGTA | 8065 |
rs761793326 | in-del | -/TTTAA | 3.35407e-05 | 0.00409503 | intron-variant | CUL5 | GRCh38.p7 | 11:108088510 | TTTCCATCAACTGCT[-/TTTAA]TTTGTTTTTTAGGGT | 8065 |
rs761804083 | snp | C/T | 1.75597e-05 | 0.00296303 | intron-variant | CUL5 | GRCh38.p7 | 11:108052817 | GTATGTTCTGAACTT[C/T]TATGATCATAATTTC | 8065 |
rs761807573 | snp | C/T | 1.65636e-05 | 0.00287776 | intron-variant | CUL5 | GRCh38.p7 | 11:108070079 | AGTAGCCTTGACTAA[C/T]TTTTGATATATTTCA | 8065 |
rs761847791 | snp | G/T | 1.71528e-05 | 0.0029285 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104399 | ATTTTGAATATCATG[G/T]ACAATATTTAGAACC | 8065 |
rs761850225 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064337 | ATTTGATCAATTTGT[A/G]TATGTTGAACCATCC | 8065 |
rs761879487 | snp | C/G | 1.67253e-05 | 0.00289178 | missense | CUL5 | GRCh38.p7 | 11:108088647 | AGAGATTGAAGCAAA[C/G]CTTAAAGAAGTGGTA | 8065 |
rs761941096 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082893 | CTGCCTCTCAAAGTG[C/T]CAGAATTACAGGCAT | 8065 |
rs761953083 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076003 | CATGAATCCAATATA[C/T]AGTATAATTTGAATT | 8065 |
rs761962456 | in-del | -/AG | 0.000190577 | 0.00975972 | intron-variant | CUL5 | GRCh38.p7 | 11:108050109 | TAATATTCTTCAGAA[-/AG]AGGGTAATTTGGAAG | 8065 |
rs761980423 | snp | C/T | 5.14664e-05 | 0.00507253 | intron-variant | CUL5 | GRCh38.p7 | 11:108009414 | TTACTGTGTGGCCGC[C/T]GGGTTCGGCTCTTTG | 8065 |
rs762030863 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080010 | ATTCTCACCAATGTT[G/T]AGTGTTCTTTTAACT | 8065 |
rs762074216 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108097089 | GTGGCACAATCTCAG[C/T]TCACTGCAACCTCCA | 8065 |
rs762096052 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018920 | GGCAAGTTACTTAAC[A/G]TCTCTGTGCCTCAGT | 8065 |
rs762109112 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052076 | ACTTAAGTGATCCTC[A/C]CACCTCAGCCTCCCA | 8065 |
rs762125609 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019959 | GCAAGAGAGTGGGGA[C/G]AGGTACCAGGCTCTT | 8065 |
rs762154515 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069084 | ACATAGCAAGACATC[A/C]TCTCTACAGAAAAGT | 8065 |
rs762166860 | snp | A/G | 9.97009e-05 | 0.00705978 | intron-variant | CUL5 | GRCh38.p7 | 11:108078258 | AAGTTTTTTAAAACC[A/G]TACTTTAAAAATACT | 8065 |
rs762168561 | snp | A/T | 1.65252e-05 | 0.00287443 | missense, intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108049935 | TTGCTAAAAGCATAT[A/T]TTGTTGAATGGCGAA | 8065 |
rs762239929 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102308 | GCTGGGATTACAGGC[C/G]TGAGCCACCATGCCC | 8065 |
rs762282556 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065807 | AAGGTGTTTTTTTGT[A/G]TGTAGATAGTTGTTA | 8065 |
rs762309920 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013384 | AAATGCAGTTCTCAC[C/T]ATATCACTTTCCTGT | 8065 |
rs762315842 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042377 | GCGTGCCTCACCACA[C/G]CAGGCTAATTTTTGT | 8065 |
rs762325184 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024168 | TTTAACAGAGCTAAA[C/G]TGCTTGGATTTGATT | 8065 |
rs762350384 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012637 | TTTCGCTCTTGTTGC[C/T]CAGGCTGGAGTGCAG | 8065 |
rs762388906 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029800 | TCCTGGTACTTAACA[A/G]TGTCTATTAGGAGAT | 8065 |
rs762406352 | in-del | -/ATTA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108073584 | TTGCATTATTTTTCT[-/ATTA]ATTATAAACTTAAAA | 8065 |
rs762483990 | in-del | -/AT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098909 | AAGTAACACCTACAC[-/AT]GATTGTTTTAATTTT | 8065 |
rs762523355 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070543 | GTGGAACCTTGTGAT[G/T]AATCTTTTTAGAATG | 8065 |
rs762525043 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043784 | CCTGTAATCCAGCAC[A/T]TTGGGAGGCCAAGGC | 8065 |
rs762532942 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014896 | GCTCTTATTATTATT[A/T]TTATTTTTATTTTTA | 8065 |
rs762540665 | snp | C/T | 0.000127186 | 0.00797351 | intron-variant | CUL5 | GRCh38.p7 | 11:108073543 | TTTAAAAGTTTTATT[C/T]TCATAATTTACTTCT | 8065 |
rs762566974 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108045471 | ATGCTTGTAGTCCCA[G/T]CTACTCAGGAGGCTG | 8065 |
rs762583422 | in-del | -/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107154 | GGAGGGGTCCCTGAG[-/T]TCTGTCAACTTTTTT | 8065 |
rs762587109 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025544 | CTCCACTATAGACTC[A/G]ATAACTTTCTGTGGA | 8065 |
rs762610962 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071834 | GCTGGAGTTACAAGC[A/G]TGAACCACCACACCC | 8065 |
rs762632202 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013920 | TAAAAAGTGCCTGTA[A/G]AAGTTATTCATTATT | 8065 |
rs762643915 | snp | G/T | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104935 | TAATAGTATCAAATT[G/T]TTCAAACATTGCTCA | 8065 |
rs762645253 | snp | A/G | 3.31625e-05 | 0.00407188 | intron-variant | CUL5 | GRCh38.p7 | 11:108089471 | ATATAAGAACTGAAA[A/G]TAACTTTATTTTTCA | 8065 |
rs762646057 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089761 | TAGCGTCAGTTAGGC[A/C]GGGCGCACTGGCTCA | 8065 |
rs762653928 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059339 | ATAGACCTAGTCCCT[A/G]TCCTCAGGATGACAC | 8065 |
rs762751421 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083143 | CTACAGTAACAAATG[G/T]CAGGGGTGAATTCAG | 8065 |
rs762795721 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064196 | ATGTTGAGGTATGTT[C/T]GTTCTATACCCAGTG | 8065 |
rs762795950 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095348 | GCCACATTTTGTTAC[A/T]TGGAAAGCTGGGAGA | 8065 |
rs762800356 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024456 | TAATAAAGGAATAAT[A/G]TCACTGAACACATAG | 8065 |
rs762825756 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035957 | AGTAAAGCCAAGATA[C/T]TGCAGGCTCGCAGCC | 8065 |
rs762844081 | snp | A/C | 5.0298e-05 | 0.00501463 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054693 | TCAAATTTATAGGGA[A/C]AATTTTGAGAAGGCA | 8065 |
rs762883913 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037232 | TTTCCTGGTTTAGAG[C/T]TATCATTTTCAAATT | 8065 |
rs762931440 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071139 | TAATATAGTTGCTTT[C/T]GTAATTATTACTCAT | 8065 |
rs762942121 | snp | C/G | 5.19458e-05 | 0.0050961 | intron-variant | CUL5 | GRCh38.p7 | 11:108009423 | GGCCGCCGGGTTCGG[C/G]TCTTTGGGAAAGGCA | 8065 |
rs763016270 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061827 | CCACATGGCCTGGGA[A/G]TCCTCAGGAAACTTA | 8065 |
rs763021135 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077500 | CCAGGCACGGTGGTG[C/T]GCACCTGTAATTCCA | 8065 |
rs763052749 | snp | A/T | 1.68386e-05 | 0.00290155 | intron-variant | CUL5 | GRCh38.p7 | 11:108046220 | TTTAAGATGTTTTGT[A/T]CAGTTCTTGTTTCAT | 8065 |
rs763068355 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013142 | TCTGGTATTATTGCT[C/T]ATTTCCTCTGCTTCT | 8065 |
rs763098876 | snp | C/T | 1.7409e-05 | 0.00295029 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104415 | ACAATATTTAGAACC[C/T]AAATTTTGGAGTGCT | 8065 |
rs763120014 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086585 | GGCTACCTAAGGGAA[G/T]ACAGAAAGACTTCCC | 8065 |
rs763128118 | snp | A/C | 3.29843e-05 | 0.00406092 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108072411 | CTTGGAGGAACATAT[A/C]ATTAGTGCTGGCCTG | 8065 |
rs763138366 | in-del | -/TTTA | 1.65255e-05 | 0.00287445 | intron-variant | CUL5 | GRCh38.p7 | 11:108104167 | GTATATTAATGCGCT[-/TTTA]TTTTTATTTTTTCTT | 8065 |
rs763140172 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087616 | AAAATTTTTTAATTT[A/G]TGTATGTTTGTGTCT | 8065 |
rs763147893 | in-del | -/ATAAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108062763 | TTATTATTTTTAAAC[-/ATAAA]ATTAAATTATTTTTT | 8065 |
rs763163140 | in-del | -/TCT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050239 | TGTCTTTAGCTTCAA[-/TCT]TCTTTCATCTTTTTA | 8065 |
rs763188561 | snp | A/G | 1.67441e-05 | 0.0028934 | missense, intron-variant | CUL5 | GRCh38.p7 | 11:108104230 | TGAGAAAGAAAATTA[A/G]TAATGCTCAGCTGCA | 8065 |
rs763194510 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075984 | GCACCCAAAGTCTAC[A/T]TAGCATGAATCCAAT | 8065 |
rs763217056 | in-del | -/TACAT | 2.34656e-05 | 0.00342524 | intron-variant | CUL5 | GRCh38.p7 | 11:108089658 | TATTTGGTTTTCTAA[-/TACAT]TACATCATTTATATG | 8065 |
rs763247596 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029608 | ACTTAGTTATGATTT[A/G]ATGATATGCTCTTCA | 8065 |
rs763298367 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066568 | CAAGGATTCTTTTAA[C/T]TCACCTTGTAATAAA | 8065 |
rs763301478 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080245 | GGACTATAAGCACAC[-/A]ACCACCATACTTTAC | 8065 |
rs763301741 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030330 | TAGTGGATATCTCCC[A/G]TGGGTCCTTATGATA | 8065 |
rs763384720 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056234 | CAACAATAGTATTTC[C/T]TCTGGTTCCTTTCAG | 8065 |
rs763420647 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090859 | TGGAACTTTAGGATA[A/G]TAAAAATTACTGTGC | 8065 |
rs763465242 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023577 | TATCCTGGGACCCTT[C/T]GGGAGTCCATGTACT | 8065 |
rs763478098 | snp | A/G | | | intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108055430 | GATGTTTCAAACTTC[A/G]TTTGTCATGAGGTAA | 8065 |
rs763502011 | snp | C/G | 1.71126e-05 | 0.00292506 | intron-variant | CUL5 | GRCh38.p7 | 11:108072322 | ACATGAATGTGTTCT[C/G]TCCTTCCAGAATTAC | 8065 |
rs763511046 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025573 | GACTCTACCCAATGC[C/T]TGGCACTTTAAAGGG | 8065 |
rs763558318 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014009 | AACAATGTCCATGCT[C/T]TTTGGGAATTTACCA | 8065 |
rs763578346 | snp | C/T | 5.17371e-05 | 0.00508585 | intron-variant | CUL5 | GRCh38.p7 | 11:108052638 | TTGAAAATTATGTTA[C/T]AATTTGTTCTTGTTT | 8065 |
rs763605873 | snp | C/T | 3.30737e-05 | 0.00406642 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094888 | CTTTGTCTCACTTCC[C/T]ACTGAACTGGAGGAC | 8065 |
rs763646698 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058822 | TAGATCTGATTTTAC[A/G]TACAATTCTAATAAG | 8065 |
rs763651861 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013011 | TTGCCCTTTAACTTA[A/G]TGATATGGCTTACTC | 8065 |
rs763696470 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048931 | TAGCCTCCCAAAGTG[C/G]TGGGATTACAGGCAT | 8065 |
rs763709282 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089765 | GTCAGTTAGGCCGGG[C/T]GCACTGGCTCATACC | 8065 |
rs763752908 | snp | A/G | 1.65113e-05 | 0.00287322 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108088617 | AACACCATTAAGCAA[A/G]AAACTAACCTCTGAA | 8065 |
rs763797134 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077317 | AGATAAACCATTGTC[C/T]TCAGCAACATGGAGG | 8065 |
rs763820552 | snp | A/C | 9.91162e-05 | 0.00703905 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094918 | CTTGATACCGGAAGT[A/C]GAAGAATTCTACAAA | 8065 |
rs763856576 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050578 | TCACCATGTTGGCCA[C/G]GCTCGTCTCGAACTC | 8065 |
rs763863365 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043912 | CCTGTAATCCCAGCT[A/G]CTTGGGAGGCTGAGG | 8065 |
rs763914160 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108097025 | TCTTAAAAGTTCCAG[A/G]TTTTTTTGTTGAGAC | 8065 |
rs763919467 | in-del | -/AGCACTTTG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108045613 | AACACTTTTAATTCC[-/AGCACTTTG]GAGACTGAGGCAGGA | 8065 |
rs763933138 | snp | A/T | 2.1606e-05 | 0.00328672 | intron-variant | CUL5 | GRCh38.p7 | 11:108098567 | CTGAAGTTTAAAAAA[A/T]CTTTAGTTTTTTTTT | 8065 |
rs763961160 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069189 | TTGAGCCTAGGAGTT[A/C]AAGGCTGTAGTGAGG | 8065 |
rs764019348 | snp | A/G | 1.68741e-05 | 0.00290461 | intron-variant | CUL5 | GRCh38.p7 | 11:108097803 | CTTGTTTGAATTTTA[A/G]CACTTTGTTTTTTGC | 8065 |
rs764039063 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024516 | AAAGTGTTTGGAACA[A/G]TACAGCACCTAACAT | 8065 |
rs764098413 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102568 | ACTCCACGACTCAAA[C/T]GATCCACCCACCTCA | 8065 |
rs764103646 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075989 | CAAAGTCTACTTAGC[A/T]TGAATCCAATATACA | 8065 |
rs764119631 | in-del | -/TGTT | 1.67444e-05 | 0.00289343 | intron-variant | CUL5 | GRCh38.p7 | 11:108046242 | TTGTTTCATTATTAA[-/TGTT]TGTTTACCTACTTTA | 8065 |
rs764129188 | snp | C/T | 1.66156e-05 | 0.00288228 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054880 | TTCTGGACAGGCAGA[C/T]GCTAAATTAAAAGAA | 8065 |
rs764141801 | snp | A/T | 1.69255e-05 | 0.00290903 | intron-variant | CUL5 | GRCh38.p7 | 11:108088487 | AATAATTGCAAACAT[A/T]AATCATTTTTCCATC | 8065 |
rs764168830 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075299 | GAACTTAATTCTGCA[A/C]GGAAACTTATTTAAA | 8065 |
rs764202092 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024740 | TTACAAAATTTGTTG[A/G]CCTTTATAATCCCCA | 8065 |
rs764207482 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041116 | TCAACAGCCTTACCA[A/G]CCTTTCTTAGAACTG | 8065 |
rs764210566 | snp | C/G | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107291 | CTGAGTAGTTAAAAA[C/G]TATTTTGCATTATTT | 8065 |
rs764239177 | snp | C/G | 5.04028e-05 | 0.00501985 | utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108009348 | GTCCAAGTTAAAGAA[C/G]ATGGCGACGTCTAAT | 8065 |
rs764242122 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028711 | CGTGGTGGTGCACAC[C/G]TGTAATCCCAGCTAG | 8065 |
rs764282689 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077819 | ATGTAGTGGTGGGCA[C/T]CTATAATCCCAGCTA | 8065 |
rs764290049 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064212 | GTTCTATACCCAGTG[C/T]TTTGATGGTTTGTAT | 8065 |
rs764294980 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029740 | TGAGTATTAGGGAAA[C/T]GTGTTTATTATGTGT | 8065 |
rs764325298 | snp | C/G | 1.66407e-05 | 0.00288446 | intron-variant | CUL5 | GRCh38.p7 | 11:108070059 | ATTTGTGCTATACAG[C/G]TTATAGTAGCCTTGA | 8065 |
rs764347440 | snp | A/C | 1.66496e-05 | 0.00288522 | intron-variant | CUL5 | GRCh38.p7 | 11:108046253 | TTAATGTTTGTTTAC[A/C]TACTTTATATTCACA | 8065 |
rs764352857 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108055775 | AGCTGGGACTACAAG[C/T]GCATGCCACCATGCC | 8065 |
rs764373289 | in-del | -/AAAC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099892 | AAGGTTGAATAACTT[-/AAAC]AAACAAAAAAAAAAT | 8065 |
rs764394603 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067949 | TTTTCCTTTTTTGAG[A/G]CGGAGTTTTGCTCTT | 8065 |
rs764416736 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023143 | AGCTACCTGGGAGGC[C/T]GAGGCAGGAGAATGA | 8065 |
rs764435342 | snp | A/C | 1.67276e-05 | 0.00289197 | missense | CUL5 | GRCh38.p7 | 11:108073442 | TTAATAGATTTAGTA[A/C]ACTCGTCAAAGAAGC | 8065 |
rs764507903 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100165 | TAAAAAAAAGGTGGT[A/G]GTGGTGGAACTTGCC | 8065 |
rs764556437 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039608 | TCAGAAACAGAAGCT[C/T]TGTACCCATTAAACA | 8065 |
rs764617111 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035887 | CCTCAGATCCAGGTA[A/G]TTGAGATCTGTGATT | 8065 |
rs764634965 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010520 | ATTAGACTCCCTGAA[-/T]TAGCCACCACTTAAA | 8065 |
rs764652765 | in-del | -/GC | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105748 | TTTATTCATTGTGGT[-/GC]GCACGTTTCAAATTT | 8065 |
rs764664154 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056903 | TCTGAGGTTTCAGCC[A/G]AGGAGAACTGTGCTG | 8065 |
rs764671922 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024348 | TGATCACTTGAGGCC[A/G]AGAGTTTGAACATGC | 8065 |
rs764678117 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101414 | TACAGCAGATGAATT[G/T]ATGGTTCATTCTTTT | 8065 |
rs764770798 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023573 | AATATATCCTGGGAC[A/C]CTTCGGGAGTCCATG | 8065 |
rs764807030 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070967 | TCTAATTAGAGTTAT[G/T]TCTGATCTATGTTGC | 8065 |
rs764823719 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083647 | GTTTTAAAAATTAGA[C/T]GAGCATGATGGTGCG | 8065 |
rs764844945 | in-del | -/GCAAC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042812 | TGTTGCCCAGGCTGG[-/GCAAC]AGTGCAGAAGTGCAG | 8065 |
rs764865325 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012027 | TTTCAGCTATGTAAA[A/G]ATTTGTGTAGCACAT | 8065 |
rs764871154 | snp | G/T | 1.70362e-05 | 0.00291853 | intron-variant | CUL5 | GRCh38.p7 | 11:108095733 | GACTGTATCCTCTCA[G/T]GTAGCAGGAAATATA | 8065 |
rs764876693 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096184 | GTTACCAAGGCAGAG[-/A]AAAAGTGCTTCAAAA | 8065 |
rs764888350 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108046925 | TTTCTGTGACACCTT[A/G]TAATGTTGTTTCAAA | 8065 |
rs764904082 | snp | C/T | 1.72033e-05 | 0.0029328 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054664 | AACCTTTGTTCTAAT[C/T]CTGAGGATAAACTTC | 8065 |
rs764918606 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012786 | ATTTTTAGTAGAGAC[A/G]GGATTTTACCATATT | 8065 |
rs764934439 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041573 | GAGCCACCATGCCCA[C/T]ACCCGGCCTGGTTTT | 8065 |
rs764953131 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018894 | TGCCATTTGCTAGCT[A/G]TGTGGTATTGGGCAA | 8065 |
rs764959095 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061809 | GGTTTAGTTGAACCA[A/G]TTCCACATGGCCTGG | 8065 |
rs764993848 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088021 | GAGATACAAATTCTT[C/T]ATTGCTTAGGAAGAA | 8065 |
rs765003133 | snp | C/T | 0.000371904 | 0.0136314 | intron-variant | CUL5 | GRCh38.p7 | 11:108088493 | TGCAAACATTAATCA[C/T]TTTTCCATCAACTGC | 8065 |
rs765004028 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058744 | TAAGTGTTGCATTAG[A/G]TGTCTGAAGCCCTAC | 8065 |
rs765017075 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048455 | TCATATATGGTTTTT[C/G]ATGTGGCTTTCTTTT | 8065 |
rs765041394 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108044950 | ATTATTAGTAGAGAT[-/G]GGGGGTTTTACCATG | 8065 |
rs765055076 | snp | G/T | 1.69864e-05 | 0.00291426 | missense | CUL5 | GRCh38.p7 | 11:108088657 | GCAAAGCTTAAAGAA[G/T]TGGTACATGAATTTT | 8065 |
rs765095841 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095359 | TTACATGGAAAGCTG[A/G]GAGATGAGCGTGTAT | 8065 |
rs765125903 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108097171 | TACAGGTGCATGCCC[C/T]ACGCTGGCTAATTTT | 8065 |
rs765144695 | snp | A/C/T | 5.02789e-05 | 0.00501372 | synonymous-codon, intron-variant | CUL5 | GRCh38.p7 | 11:108104228 | AATGAGAAAGAAAAT[A/C/T]AGTAATGCTCAGCTG | 8065 |
rs765195678 | snp | A/G | 1.73408e-05 | 0.0029445 | intron-variant | CUL5 | GRCh38.p7 | 11:108072309 | AAATGAAATGATTAC[A/G]TGAATGTGTTCTCTC | 8065 |
rs765237367 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095205 | GAATTCAACATGATC[C/G]CAACTATCTCAGTAT | 8065 |
rs765239656 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080470 | GTCTGATCTTGTCTT[A/C]CTGCAACATCCACCT | 8065 |
rs765248786 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102992 | ATAGAGATGGGGTTT[C/T]GCCATGTTGCCCAGG | 8065 |
rs765265154 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037195 | CATGGCCAGAAACTG[A/C]CAGGGGAATGAGGTA | 8065 |
rs765292447 | snp | A/G/T | 8.83391e-05 | 0.0066455 | intron-variant | CUL5 | GRCh38.p7 | 11:108052822 | TTCTGAACTTTTATG[A/G/T]TCATAATTTCTGTTT | 8065 |
rs765299296 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079512 | CAGTCAACTTTTTAA[G/T]TGTATTTCTAAAGAA | 8065 |
rs765326718 | snp | A/G | 5.03749e-05 | 0.00501846 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108009369 | GACGTCTAATCTGTT[A/G]AAGGTAAGACCCTCA | 8065 |
rs765354314 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108044818 | CCAGGCTGGAGTTCA[C/T]TGGTGCCATCTTGGC | 8065 |
rs765382238 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038854 | TCTTTCTAAATCTTA[G/T]TTACTAAATAATGTA | 8065 |
rs765428469 | snp | A/G | 1.65395e-05 | 0.00287567 | intron-variant | CUL5 | GRCh38.p7 | 11:108070087 | TGACTAATTTTTGAT[A/G]TATTTCAGCTCATGG | 8065 |
rs765447661 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075158 | GGAGGCTTGTCCCAG[A/C]GTGATGGTAGAGGTG | 8065 |
rs765476237 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077450 | CAGGAGTCAACATGA[A/T]GAAACCCTGTCTCTA | 8065 |
rs765478297 | snp | C/G/T | | | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074319 | CCTGCCTCAGCCTCT[C/G/T]GAGTAGCTGGGATTA | 8065 |
rs765479582 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060814 | TCCAGCTTGGGCAAC[A/G]AGTGAAACTGTCTCA | 8065 |
rs765531752 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066459 | AGTCACTCTACTCCA[A/G]TAAGAAATATTTTTT | 8065 |
rs765542200 | in-del | -/T | 1.65762e-05 | 0.00287886 | frameshift-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108052699 | CAATCTTTTCAAACA[-/T]TAAAAAACAGACTCC | 8065 |
rs765550777 | in-del | -/GA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108073302 | TCCCCAGTTTTAAAT[-/GA]GTTTTATTAAAATTA | 8065 |
rs765594369 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065481 | GTCCTTACCACTGGA[A/G]TGGGCGATTCCCCTC | 8065 |
rs765603747 | in-del | -/TTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069541 | AAAGTAGTTTCTAAG[-/TTT]TTTTTTATTTTGTGT | 8065 |
rs765653262 | snp | A/G | 3.30175e-05 | 0.00406296 | synonymous-codon, intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108049952 | TGTTGAATGGCGAAA[A/G]TTCTTTACACAATGT | 8065 |
rs765669621 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009208 | AGGTCAGCGCTGTCG[A/G]CGCGCTGCTCCAGCG | 8065 |
rs765781735 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048365 | ATTTGGGCTGGTCTC[A/T]GATGAATTTGCCTAA | 8065 |
rs765831171 | snp | A/G | 1.67433e-05 | 0.00289333 | missense | CUL5 | GRCh38.p7 | 11:108073463 | TCAAAGAAGCTTTTC[A/G]AGATGATCCACGATT | 8065 |
rs765839872 | snp | C/T | 3.82468e-05 | 0.00437286 | intron-variant | CUL5 | GRCh38.p7 | 11:108094540 | ATAATTACATGTATA[C/T]ATTTTTTAAACTTAG | 8065 |
rs765882487 | in-del | -/T/TT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042223 | TCCACAATTCTTTTT[-/T/TT]TTTTTTTTTTTTTTG | 8065 |
rs765915858 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042796 | GAGACAGAGTCTTGC[A/C]CTGTTGCCCAGGCTG | 8065 |
rs765957827 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033230 | GTATGACAGTATGCA[C/T]GAGTACCATCAAATA | 8065 |
rs765992789 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096978 | CATTAGCCCCCTGCT[C/T]ACAACTACATTTTAT | 8065 |
rs766010888 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022410 | AAATACTGTATTTCT[A/G]CACCATTATATATCT | 8065 |
rs766030046 | snp | C/T | 4.25469e-05 | 0.00461212 | intron-variant | CUL5 | GRCh38.p7 | 11:108073544 | TTAAAAGTTTTATTC[C/T]CATAATTTACTTCTA | 8065 |
rs766031826 | snp | C/T | 1.64991e-05 | 0.00287215 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108046319 | GGCCCAGCAAAAATT[C/T]ATCAGGCTTTAAAAG | 8065 |
rs766041408 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059745 | AAAAATTAGTTGGGC[A/G]TGGTGGCACGCACCT | 8065 |
rs766071382 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023376 | ATACATTTTTTTCCC[G/T]TTATGGTTAATGCTT | 8065 |
rs766101487 | snp | C/G | | | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074115 | TTCGTTACTTCCCAA[C/G]TTTGAATGATTCTAA | 8065 |
rs766103624 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023977 | TTTTACGTAGTGATG[-/T]TTCCGCCGTATGGTT | 8065 |
rs766112965 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040646 | AAAAATTAGCCAGTC[A/G]TGGTGGCACGTGCCT | 8065 |
rs766125521 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069155 | CTAGCTACTCAAGAG[G/T]CTGAGGCAGGAGGAT | 8065 |
rs766192981 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068513 | AATGTAGGAAGAACA[-/G]TATAATGAATCCCCA | 8065 |
rs766193794 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053234 | GCTTCATCCTCCTCC[-/T]TGGAGGCCTTTCTTA | 8065 |
rs766205636 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060701 | AATTACCCGGGCATG[G/T]TGGTGCGTGCCTGTA | 8065 |
rs766217854 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028468 | TGCTTCCTAATCCTA[C/T]ACCCAGTTTTAACCC | 8065 |
rs766221838 | in-del | -/TG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108074979 | GGAGTTAGTTTTTAC[-/TG]TGAGTAGGATGGGAA | 8065 |
rs766223601 | snp | A/G | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105912 | GTAGGATCTGTCCCC[A/G]TCCGAAGAGGCTTTG | 8065 |
rs766240732 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016547 | GAGCTACCACCCCTA[C/T]TTGAGGTTTCTCTTA | 8065 |
rs766273627 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026630 | TTCTCTCCCTTTCCC[C/G]ACATCATCAACATTT | 8065 |
rs766345643 | snp | C/G | 4.9467e-05 | 0.00497303 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033884 | GCCAGGAATCTGTTA[C/G]AAAACAGCAGTGGTT | 8065 |
rs766366052 | snp | A/T | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007112 | TTTTATTATTTTTTA[A/T]AGCGATAGCTACTTT | 8065 |
rs766370690 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095268 | CTTACACCTTTCATT[A/G]GGGACAACTTCTAGA | 8065 |
rs766387091 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108091847 | AGTCATTAGTGAAAT[A/G]CAAGTGAAATGCTCA | 8065 |
rs766402698 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065934 | GTCTCACTATGTTGT[-/C]CAGCCTGGTCTGCAT | 8065 |
rs766408627 | snp | A/G | 1.66827e-05 | 0.00288809 | synonymous-codon, intron-variant | CUL5 | GRCh38.p7 | 11:108104240 | AATTAGTAATGCTCA[A/G]CTGCAGACTGAATTA | 8065 |
rs766439384 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020063 | GGCATTCATCTGTAC[A/G]TGAGGGATCCACCAC | 8065 |
rs766442617 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098331 | TTTTAAATCTTTTCT[C/G]TCAGACATTGTTGCT | 8065 |
rs766461900 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042218 | AGTCATCCACAATTC[-/T]TTTTTTTTTTTTTTT | 8065 |
rs766464623 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108091763 | GCAGGCAAAGGATTC[A/G]AATTGACATCTCTTC | 8065 |
rs766514769 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066284 | AGGAGGCAGAGCTTG[C/T]AGTGAGCCAAGATCA | 8065 |
rs766532703 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009106 | CCGTTCCGGTCTTCC[C/T]GAGCGCGTGCATGAG | 8065 |
rs766547153 | snp | A/T | 2.04908e-05 | 0.00320077 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033756 | AGGATACTTTTTATT[A/T]AACTGCATTTAAATT | 8065 |
rs766568218 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053417 | GTTAATGAACCTATA[C/G]AGTTACTTTTGACTG | 8065 |
rs766605308 | snp | C/T | 1.75468e-05 | 0.00296194 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104421 | TTTAGAACCCAAATT[C/T]TGGAGTGCTTGGGCA | 8065 |
rs766631620 | snp | C/T | 3.32336e-05 | 0.00407624 | missense | CUL5 | GRCh38.p7 | 11:108072461 | CTGAAACTATTACTA[C/T]TGTAAGTTTTTTTTC | 8065 |
rs766652147 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072251 | ACAGAATACTATTAA[C/T]ATTACAAACTTAACT | 8065 |
rs766652211 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085473 | CAAGATTTCTGTTTG[C/G]GATAATGAAGAAGTT | 8065 |
rs766673495 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016012 | CTGCAGTCTTGATCT[C/T]CCAGGATCAAGCGAT | 8065 |
rs766696136 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076375 | TCATGCTGTACATTA[A/G]CTCTCTAGACTTTTT | 8065 |
rs766703608 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042637 | GGAACCAACTATTCC[A/G]GGAAGCCTTTCCTTT | 8065 |
rs766708780 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018284 | CATAGAATTGCAGTA[A/G]TAAGAATTACTGGTA | 8065 |
rs766713346 | in-del | -/CTTC | 1.68055e-05 | 0.0028987 | intron-variant | CUL5 | GRCh38.p7 | 11:108094365 | ATGTATTTATTACCT[-/CTTC]CTTCTTTGGTTTATA | 8065 |
rs766802981 | snp | C/T | 1.65233e-05 | 0.00287426 | missense | CUL5 | GRCh38.p7 | 11:108094911 | TGGAGGACTTGATAC[C/T]GGAAGTAGAAGAATT | 8065 |
rs766809886 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031422 | CTGGTGTACTAGAAA[A/G]TTAGGTTTTACATTT | 8065 |
rs766841025 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013837 | ACTTTGGGAGGATGA[C/G]GTGAGAGGATTACCT | 8065 |
rs766867443 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064375 | CACGGATAAATCCCA[C/T]TTGGTCATGATGAAT | 8065 |
rs766893955 | snp | A/G | 0.000190422 | 0.00975575 | intron-variant | CUL5 | GRCh38.p7 | 11:108094562 | TAAACTTAGAAGAAT[A/G]TCTTTGTTTTCCAGT | 8065 |
rs766898170 | in-del | -/T | 0.000481768 | 0.015513 | intron-variant | CUL5 | GRCh38.p7 | 11:108054859 | TTAAAATGATTGCTA[-/T]TTTGCTTCTGGACAG | 8065 |
rs766899163 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108091506 | ATGAGCCTGGGCAAC[A/G]TGGTGAAACCCCATC | 8065 |
rs766915698 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060554 | CTAAAAGAAGAATCT[A/G]GCTGGATGCCGTGGC | 8065 |
rs766983320 | snp | G/T | 1.65192e-05 | 0.00287391 | missense, intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108050022 | TTAATGGGTAAACAG[G/T]GCAGCAATAAAAAAT | 8065 |
rs766984881 | in-del | -/ATTAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108078398 | CATTTATAATTTTTT[-/ATTAA]ATTAAATTATTTTAC | 8065 |
rs766992973 | snp | C/T | 2.02227e-05 | 0.00317977 | intron-variant | CUL5 | GRCh38.p7 | 11:108078136 | TTTATCTGTATATTT[C/T]CAATATTAAAAATAT | 8065 |
rs767001603 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015059 | GACCACCACCATGCT[C/T]GGCTGATTTTTGCAT | 8065 |
rs767013984 | in-del | -/TTTTTTTTTTTTTTTTTTTTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048651 | TAGACTCCACCACCT[-/TTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 8065 |
rs767023056 | snp | A/G | 3.333e-05 | 0.00408214 | intron-variant | CUL5 | GRCh38.p7 | 11:108078291 | AATTTTCTTTAGTGT[A/G]ATAGGGGTTAACTAG | 8065 |
rs767074602 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023750 | TCTGTCAGTTTTATT[A/C]TTCTTGCTTTTTCCT | 8065 |
rs767134834 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108078918 | GTTGCTTGAGTAATA[C/T]TACAGTGGAAGACAT | 8065 |
rs767151660 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108091416 | ACAAACAAGGCTAGG[C/T]ATGGTGGCTCACACC | 8065 |
rs767187203 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037556 | CCAGGAGAAACGAAA[A/T]CCAAACTTCCAAATG | 8065 |
rs767204507 | snp | A/T | 1.82244e-05 | 0.00301859 | intron-variant | CUL5 | GRCh38.p7 | 11:108098561 | GAATGTCTGAAGTTT[A/T]AAAAAACTTTAGTTT | 8065 |
rs767219636 | snp | A/G | 1.77021e-05 | 0.00297502 | intron-variant | CUL5 | GRCh38.p7 | 11:108052619 | ATACTTTGTATATTA[A/G]TAATTGAAAATTATG | 8065 |
rs767230830 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084355 | GTTTCCCTAAGGAGA[C/T]GCAGCAGCTGAGAAT | 8065 |
rs767272071 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037378 | CTTCATGAGTCCAAC[-/T]TCTAACACCAGCTGT | 8065 |
rs767321348 | in-del | -/AAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026989 | GTGAGACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 8065 |
rs767323849 | snp | A/G | 1.71587e-05 | 0.002929 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009299 | GTCAAGGCCTGGCCG[A/G]GAGCGCCACGAATTC | 8065 |
rs767324769 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025939 | TGTAGCGCTCACCTC[A/G]TTTGTTTTTCTTTTC | 8065 |
rs767366473 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072203 | AAAACAACAACAAAA[A/G]AACGAACAACTACTC | 8065 |
rs767375979 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026715 | AAATTATTTGGCCAG[A/G]CGCAGTGGCTCACGT | 8065 |
rs767387694 | snp | G/T | 1.68547e-05 | 0.00290294 | utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108009339 | CTCGCGAGAGTCCAA[G/T]TTAAAGAACATGGCG | 8065 |
rs767406160 | in-del | -/GAGT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077932 | CCAGCCTGGTCGACA[-/GAGT]GAGACTTCATCTCAA | 8065 |
rs767407131 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008740 | TTGAAGACAGCTGTT[G/T]TAAGCATTTCAGGAC | 8065 |
rs767441892 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088976 | AGATTGGGAGTTTTT[C/G]ACTCCTTCCTTTTTG | 8065 |
rs767502184 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082917 | CAGGCATGAGCTACC[A/G]TGCCCAACCACAAAT | 8065 |
rs767560650 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059616 | GGGCGCGGTGGCTCA[C/T]GCCTGCAATCCCAGC | 8065 |
rs767632295 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030552 | TGAGGCAGGAGAATC[C/G]CTTGAACCCGGGAGG | 8065 |
rs767640595 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050931 | CCTTTCAGCTCTTCA[A/G]ACTCCGTCCTCATTT | 8065 |
rs767669899 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010723 | CTTTAAGAAAACTAA[-/T]TTCGGGGAATTGAGT | 8065 |
rs767682450 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108097956 | GATACATTTTTGGTC[C/T]CTGACATTATACTGT | 8065 |
rs767685369 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018924 | AGTTACTTAACATCT[C/G]TGTGCCTCAGTTTCT | 8065 |
rs767688311 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083415 | TCTACAAGATAGAGT[C/T]CCAGAAGTGAGGATT | 8065 |
rs767692876 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108097137 | ATCCTCCCACCTGAG[C/T]CCCCCAAGTAGCTGG | 8065 |
rs767705560 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056425 | TTTGTTCAGAAATCA[C/T]ACCGAGTTGGATGTC | 8065 |
rs767729201 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102316 | TACAGGCGTGAGCCA[C/T]CATGCCCGGCCTATT | 8065 |
rs767731531 | snp | A/G | 1.68556e-05 | 0.00290302 | intron-variant | CUL5 | GRCh38.p7 | 11:108094345 | TCCCAGTAATATATC[A/G]GATTATGTATTTATT | 8065 |
rs767739701 | snp | C/T | 1.66635e-05 | 0.00288643 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054712 | TTTGAGAAGGCATAC[C/T]TGGATTCAACAGAGA | 8065 |
rs767744611 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030759 | ATAAGAGTATGATGT[C/T]AATTTGTGGTTCTTA | 8065 |
rs767783081 | snp | A/C | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108006948 | TCAGTGTTTCTACCC[A/C]ACCATCAGTTCATCT | 8065 |
rs767800651 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040020 | CTACACAAGGAAATC[A/G]AAACCTCTGGAATAG | 8065 |
rs767835815 | snp | C/T | 3.08828e-05 | 0.00392943 | intron-variant | CUL5 | GRCh38.p7 | 11:108095502 | CATCATGAGATTCTT[C/T]ATTAAAAATCTGTTT | 8065 |
rs767841510 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036239 | TAAAAAAGTCATAGT[A/G]AATATCATCCATTGT | 8065 |
rs767882111 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086857 | AAATACTGGTATTGA[G/T]GTACATAGAATTCAT | 8065 |
rs767901682 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041189 | CAGGGATCACACCTA[C/T]ACCCAGCTTTCTGTA | 8065 |
rs767909166 | in-del | -/T | 0.000117266 | 0.00765631 | intron-variant | CUL5 | GRCh38.p7 | 11:108095702 | ATGGGTTGGTTTATG[-/T]TTTTTTTGTTTTTAA | 8065 |
rs767912682 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058771 | CTACTCTTACAGTTT[C/T]ATTTTTACTTATAGG | 8065 |
rs768085042 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076698 | GTTATCTTTGTGAAG[-/T]GGTGATTTCATTTCC | 8065 |
rs768217449 | in-del | -/TTTTA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065894 | CTCCACTCCTCTATT[-/TTTTA]TTATTTTTTTTAGAA | 8065 |
rs768224932 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071966 | AGGATTGTGTGAGCC[C/T]CGAAGTTTGAGACCA | 8065 |
rs768226352 | snp | G/T | 2.04882e-05 | 0.00320058 | intron-variant | CUL5 | GRCh38.p7 | 11:108054630 | ATTGGAGTAATACTT[G/T]ATTTTCTGTTTTTCA | 8065 |
rs768247635 | snp | A/C/G/T | 4.09234e-05 | 0.00452331 | intron-variant | CUL5 | GRCh38.p7 | 11:108088709 | TACCTTACTTTGAAT[A/C/G/T]TGTGTTTTGCTTATA | 8065 |
rs768301255 | snp | A/G | 1.66034e-05 | 0.00288122 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054772 | TTACAACAAAATGGT[A/G]TACAGAATTATATGA | 8065 |
rs768312982 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108073690 | AACATTAGATAGCCT[C/T]GTGAATTAGAATTTA | 8065 |
rs768326515 | snp | C/T | 1.65002e-05 | 0.00287225 | missense | CUL5 | GRCh38.p7 | 11:108072377 | AAGTTCCTAATGGTA[C/T]AGAGCCAATGTTGAA | 8065 |
rs768335630 | snp | C/T | 3.38484e-05 | 0.00411376 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104385 | ATATATATGGCATAA[C/T]TTTGAATATCATGGA | 8065 |
rs768352677 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108054820 | TTAGTATATGTGATA[A/G]TTTGAGCAATTCCCT | 8065 |
rs768418231 | in-del | -/TAGGGGTTAAC | 1.66643e-05 | 0.0028865 | intron-variant | CUL5 | GRCh38.p7 | 11:108078293 | TTTTCTTTAGTGTAA[-/TAGGGGTTAAC]TAGGTATACAAAGTA | 8065 |
rs768441776 | snp | A/G | 4.06108e-05 | 0.00450597 | intron-variant | CUL5 | GRCh38.p7 | 11:108089631 | GGCTAAGAGTAAGTA[A/G]ATTTTTTTAAATATT | 8065 |
rs768453349 | in-del | -/TAAT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103482 | TATTTGTAGCAAATA[-/TAAT]TAATTAATCTGGTAA | 8065 |
rs768459078 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098093 | TTTTGTTTGTTAAGA[C/G]CCAGTTAGGCAATAA | 8065 |
rs768470549 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108074673 | TAGCTGGACGTGGTG[C/G]TACATGCGTGTAATT | 8065 |
rs768477004 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064967 | TCAGCAGTGAAGCCA[G/T]CAGGTGCCAGGCTTT | 8065 |
rs768493085 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052822 | TTCTGAACTTTTATG[-/A]TCATAATTTCTGTTT | 8065 |
rs768519665 | snp | C/T | 1.67713e-05 | 0.00289575 | intron-variant | CUL5 | GRCh38.p7 | 11:108033938 | ACTAATTCTGTTTGC[C/T]AGCATAAAGGAAATT | 8065 |
rs768545028 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083973 | TTCCGTAAAACATTA[C/T]GAGATTTTTTGGCGA | 8065 |
rs768592427 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033283 | GTTGAGTTTTGATGG[-/A]AGCTTATTCACATAG | 8065 |
rs768596829 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063241 | TATCCTTTACTCTCT[A/G]TTTCCATGAGTTCAA | 8065 |
rs768609343 | snp | G/T | 1.64993e-05 | 0.00287218 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033840 | AGACAAATGGGATTT[G/T]ATGCGCCCGATTGTT | 8065 |
rs768612129 | snp | A/C | | | intron-variant, utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108073931 | AGTTATGTTATACTT[A/C]TCCTTGTTTCCCAGG | 8065 |
rs768613015 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019815 | AATACCTGAGACTGG[A/G]TAATTTATAAAGAAA | 8065 |
rs768624380 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009320 | CCACGAATTCTCGCG[G/T]CGTCTCGCGAGAGTC | 8065 |
rs768644379 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101170 | TAGGTAATGCTCAGA[C/T]TTTATTTCCTCCTGA | 8065 |
rs768645121 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042079 | AAATATAATAGGACT[C/G]TGATTGAATATAAGG | 8065 |
rs768657736 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013597 | TAACTCTTAACTTTC[A/G]TTCTCTCTCCTTCTG | 8065 |
rs768698580 | snp | C/T | 1.69372e-05 | 0.00291004 | intron-variant | CUL5 | GRCh38.p7 | 11:108095014 | GTGTGTTAGTTATTT[C/T]AGCTTTCAGTTTGGA | 8065 |
rs768711943 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015489 | TGTCAATTTTTCATT[A/G]GGTTGATAGAAATTG | 8065 |
rs768719121 | snp | C/T | 0.000298238 | 0.0122078 | intron-variant | CUL5 | GRCh38.p7 | 11:108104186 | TTTTTATTTTTTCTT[C/T]TAGGAAGCTATCATA | 8065 |
rs768729427 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009647 | GGACCAGCTCTGGCC[C/G]GGAGCGGGAGATGAA | 8065 |
rs768786811 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102988 | TTTTATAGAGATGGG[A/G]TTTCGCCATGTTGCC | 8065 |
rs768843350 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081518 | AGCACTTAGGGAGGC[C/T]GAGGCGGGCAGATCA | 8065 |
rs768851778 | in-del | -/T | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108006978 | TTATTTTTTGATACA[-/T]TTCCAAGTAAATTAT | 8065 |
rs768859423 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043424 | ATTAGATGAGACTGT[A/G]TAGGTATGCAGGAGT | 8065 |
rs768878676 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088883 | TAATTCCTCTCCTTT[C/T]TTGGTTATTTTTAGG | 8065 |
rs768892392 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081889 | ATAAGCTTTAAAAGC[A/G]AGATGTGTGCATGTT | 8065 |
rs768963400 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076741 | CCTAGAAGAGGGATT[A/G]CTGGGATTATGATTA | 8065 |
rs768974489 | snp | A/G | 1.71658e-05 | 0.00292961 | intron-variant | CUL5 | GRCh38.p7 | 11:108050095 | TCTCCTTGTTTTCCT[A/G]ATATTCTTCAGAAAG | 8065 |
rs768974607 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082559 | TAGGATTACGGGCAG[C/G]AGCTACCATGCCCAG | 8065 |
rs769063205 | snp | G/T | 1.6492e-05 | 0.00287154 | missense | CUL5 | GRCh38.p7 | 11:108097724 | TTACAGAAGGTACCC[G/T]CTTCTCAGTGAACCA | 8065 |
rs769065948 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093772 | GAGCGCAGTGACACA[A/G]TCAGAGCTTAAACTC | 8065 |
rs769103279 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096089 | CAACAGAGTGAGAAC[G/T]CCGTCTGAAAAAAAA | 8065 |
rs769124510 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068086 | GGCACCCACCATGCC[C/T]GGCTAATTTTTAGTA | 8065 |
rs769158218 | snp | C/T | 1.69989e-05 | 0.00291533 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094462 | AAAAGTATCTGAAGA[C/T]TTGAACCAAGCTTTT | 8065 |
rs769169523 | snp | A/G | 1.65927e-05 | 0.00288029 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108078232 | TGAATTACCTTTGAA[A/G]CAGAAGGGGTAAGTT | 8065 |
rs769193538 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035070 | AGGGGTGACAGGAAA[G/T]AGAGAACTAGAGTCA | 8065 |
rs769219050 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012524 | TATGTCCCCTCTTAC[C/T]TTTTTTTTTTTTTTT | 8065 |
rs769231962 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035477 | CAAAGTGGCTTACGC[C/T]TGTAATCCCAGAACT | 8065 |
rs769266636 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038253 | AGTCTGTGTTGATAA[G/T]ATTTATTATTGAGAA | 8065 |
rs769295204 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037707 | GGGGCTCGTCATGTA[A/G]GCAGCTTCTGCCTGG | 8065 |
rs769318515 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052513 | GCGATCCACCTGCCT[C/T]GGCCTCCCAAATTGT | 8065 |
rs769347067 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102263 | TCGAACTCCTGACTT[C/T]GTAATCCGCTCCCCT | 8065 |
rs769402039 | snp | A/T | 3.32403e-05 | 0.00407664 | intron-variant | CUL5 | GRCh38.p7 | 11:108054815 | AGAACTTAGTATATG[A/T]GATAATTTGAGCAAT | 8065 |
rs769407237 | snp | A/T | 4.20681e-05 | 0.00458609 | intron-variant | CUL5 | GRCh38.p7 | 11:108089640 | TAAGTAAATTTTTTT[A/T]AATATTTGGTTTTCT | 8065 |
rs769409356 | snp | A/T | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007941 | CGGCTAATTTGTGTA[A/T]TTTTAGTAGAGACAG | 8065 |
rs769417565 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025511 | TCCAGAATATCACTC[A/G]GGGTAGGGCTACTTT | 8065 |
rs769420013 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030561 | AGAATCGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 8065 |
rs769430111 | snp | A/G | 1.72003e-05 | 0.00293255 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104403 | TGAATATCATGGACA[A/G]TATTTAGAACCCAAA | 8065 |
rs769455048 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083928 | GCCCAGGACGGCTTT[A/G]AACGTGGCCCAACAC | 8065 |
rs769462644 | snp | A/G | 1.70353e-05 | 0.00291846 | intron-variant | CUL5 | GRCh38.p7 | 11:108033959 | AAAGGAAATTTTAGT[A/G]ATGTCTTTCCATACC | 8065 |
rs769507945 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076640 | GCTGAGGTTGTGTCC[A/G]TATTTTTGCTATTGT | 8065 |
rs769510093 | snp | C/G | 3.40107e-05 | 0.00412362 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009324 | GAATTCTCGCGTCGT[C/G]TCGCGAGAGTCCAAG | 8065 |
rs769544597 | in-del | -/TT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012525 | ATGTCCCCTCTTACT[-/TT]TTTTTTTTTTTTTTC | 8065 |
rs769570478 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060388 | AAAGTGGGGGAACTT[-/A]AAGATAATTTTTAGT | 8065 |
rs769574939 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075948 | CTCATTTTCTTGTTT[C/T]GTTTTGTTTTTGTGG | 8065 |
rs769598770 | snp | A/G | 5.15008e-05 | 0.00507422 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054947 | CGAGAATGTAACTCC[A/G]TTGAAGCAGTAAGTA | 8065 |
rs769613037 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071499 | ACTGCTTCTGGCCAA[A/G]TGACTGACCTTTTAA | 8065 |
rs769627030 | snp | A/G | 1.66145e-05 | 0.00288218 | intron-variant | CUL5 | GRCh38.p7 | 11:108089448 | TAAATTCGAGAGATG[A/G]TAAGAGTATATAAGA | 8065 |
rs769679784 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096754 | TATTTTTAGTGGAGA[C/T]GGGGTTTCACCATGT | 8065 |
rs769750061 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034999 | ACATCAGTTCCTTTC[C/T]GGGGACAGCTGCATT | 8065 |
rs769765207 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030144 | TGTGAGGCCAGGCAT[A/G]AAGTTATTGTACAAA | 8065 |
rs769780964 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064693 | GCAGCCTGGGCAACA[A/G]AGTGATACTCTGTCT | 8065 |
rs769839796 | snp | A/G | 2.18649e-05 | 0.00330635 | intron-variant | CUL5 | GRCh38.p7 | 11:108073363 | CTTTTTCTTTTAAAA[A/G]CTTAATGTAAAACCT | 8065 |
rs769855877 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039182 | TGCACCACCACACCT[C/G]GCTAATTTTTTGTAT | 8065 |
rs769873696 | in-del | -/TAAAA | 1.65688e-05 | 0.00287821 | intron-variant | CUL5 | GRCh38.p7 | 11:108104140 | TCAGTTTGTTGTACT[-/TAAAA]TAATTTCGTATATTA | 8065 |
rs769888981 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086463 | CTGTCCTCTTGATAG[A/G]TTGAATGAAGGAGGG | 8065 |
rs769899704 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011339 | TGGAAGCTACTTTGG[G/T]TCATATTAGTTAAGT | 8065 |
rs769903820 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023954 | CACCATGTTTGAAAA[G/T]AAATGTCTTTTACGT | 8065 |
rs769952602 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012327 | TTTCTTGCTGAGCCT[C/T]ACCCCTCTTAATTCT | 8065 |
rs769974016 | snp | A/G | 1.69916e-05 | 0.00291471 | intron-variant | CUL5 | GRCh38.p7 | 11:108095022 | GTTATTTCAGCTTTC[A/G]GTTTGGATGAAAGTA | 8065 |
rs769988633 | snp | C/T | 1.64885e-05 | 0.00287123 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033868 | GTTTTGAAGCTTTTA[C/T]GCCAGGAATCTGTTA | 8065 |
rs770000912 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057346 | ACGGTCAAAAGTTTG[A/C]AATGAAATAGGATAT | 8065 |
rs770026212 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108045722 | AAAAAAAAATTAGGC[A/G]TGGTGGCATGCTCCT | 8065 |
rs770032877 | in-del | -/G | 2.0684e-05 | 0.00321583 | intron-variant | CUL5 | GRCh38.p7 | 11:108088711 | CCTTACTTTGAATTT[-/G]TGTTTTGCTTATAGG | 8065 |
rs770077788 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092572 | ACTTTGAAAACATAA[G/T]GCTGAGTGAAAGAAG | 8065 |
rs770080018 | snp | C/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032972 | ACTATTCTCACTTCT[C/G]ACACCAACTGTAAGC | 8065 |
rs770120509 | snp | A/G | 0.000149488 | 0.00864417 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108088527 | TAATTTGTTTTTTAG[A/G]GTGGGATTAAAAACT | 8065 |
rs770121409 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087584 | AATATAGATAGTGAG[A/G]CCTTGTCTGAATTTA | 8065 |
rs770122104 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102126 | TCCCAGGTTCAAATG[A/C]TTCTCCTGCCTCGGA | 8065 |
rs770173167 | snp | C/T | 3.29875e-05 | 0.00406112 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108095586 | AACCACGTTTCAGCT[C/T]GCTGTATTGTTTGCA | 8065 |
rs770220380 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023529 | GTGTCTGGTTGAAGT[C/T]GTTGTTTGAAAAAAG | 8065 |
rs770226989 | snp | A/T | 0.000154773 | 0.0087956 | intron-variant | CUL5 | GRCh38.p7 | 11:108054601 | TTATACTCAAAATAC[A/T]GATTTTGATCATAAT | 8065 |
rs770254734 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061482 | AAAAGCTTTGTAATG[A/C]AAGTTTTAAAATATT | 8065 |
rs770313605 | in-del | -/TTTTTTTTT | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007754 | TTTTTTTGTTTGTAG[-/TTTTTTTTT]GTTTTTTTTGTTTTT | 8065 |
rs770316737 | snp | A/G | 1.65704e-05 | 0.00287836 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108052721 | ACAGACTCCAAGATA[A/G]TGCAATGAAGCTGGT | 8065 |
rs770326835 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081451 | AACAGTCTTTTCTCC[A/G]TTATCAAAAATCGGT | 8065 |
rs770335374 | snp | A/G/T | 4.9925e-05 | 0.00499604 | intron-variant | CUL5 | GRCh38.p7 | 11:108070217 | TCACATAAAGTTATC[A/G/T]TAATCTTCTAAGAGG | 8065 |
rs770337479 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017308 | GTTGGGAGGCTTGCT[G/T]GAGCCCAGGAGGTTG | 8065 |
rs770429406 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051498 | AAATGAGTTACATGC[A/G]GACAATACATAGAGC | 8065 |
rs770438229 | in-del | -/TTAAAAG | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032165 | ACATGTACCCCAAAC[-/TTAAAAG]TTAAAGAAAATCGTG | 8065 |
rs770451795 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030156 | CATAAAGTTATTGTA[C/G]AAAGTATATGCCGCA | 8065 |
rs770495861 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108094605 | AACCTCAGCAGTAAT[A/G]GATCGAAAGATGTTA | 8065 |
rs770497169 | snp | A/G | 1.6495e-05 | 0.0028718 | missense | CUL5 | GRCh38.p7 | 11:108098492 | TGAGAGAAGAAGAGA[A/G]TGAAGGAATAGTTCA | 8065 |
rs770531808 | snp | C/G | 1.69132e-05 | 0.00290797 | intron-variant | CUL5 | GRCh38.p7 | 11:108009394 | CCCTCACTCCAGCTT[C/G]GGTTTTACTGTGTGG | 8065 |
rs770551089 | snp | C/G | 1.69622e-05 | 0.00291219 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009328 | TCTCGCGTCGTCTCG[C/G]GAGAGTCCAAGTTAA | 8065 |
rs770593731 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100417 | CTGTGGTGGCGCATG[C/G]CTGTAATCCCAGCTA | 8065 |
rs770649653 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086392 | CCCAGGAGTTCAAGA[C/T]CAGCCTGAGCAATGT | 8065 |
rs770684168 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070545 | GGAACCTTGTGATGA[A/G]TCTTTTTAGAATGTA | 8065 |
rs770703668 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029197 | GTGCTGTAAGGAGTG[A/G]AGGATAGAATACCTT | 8065 |
rs770739602 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108074916 | AATTGAGTAGCCTGC[A/G]AAGGCTTCATAGGAA | 8065 |
rs770834911 | snp | G/T | 1.84276e-05 | 0.00303537 | intron-variant | CUL5 | GRCh38.p7 | 11:108054982 | TGTAATTGTACATTT[G/T]ATGGGATTATTTGAA | 8065 |
rs770899204 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075733 | CTATAGAGACAACAT[C/G]TAGCTATGTTGTTTG | 8065 |
rs770932993 | snp | A/T | 1.82231e-05 | 0.00301848 | missense | CUL5 | GRCh38.p7 | 11:108094488 | CTTTTAAGGAAATGC[A/T]CAAAAATAATAAATT | 8065 |
rs770959497 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082048 | TTGTATTAATGTTAT[A/G]TCTCCCAATTATGAA | 8065 |
rs770985989 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063747 | CATTCTTTTTGGTAT[A/G]TAGCCAGCAGTGGGA | 8065 |
rs771022629 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010012 | ATGAAGCGATACCAT[A/C]GTTTTAGGGCGCAGG | 8065 |
rs771044373 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108021560 | GATTATCATAGGTCA[C/T]TGCAGCCTTGAATTC | 8065 |
rs771047052 | in-del | -/TTTT | 1.84487e-05 | 0.0030371 | intron-variant | CUL5 | GRCh38.p7 | 11:108104177 | GCGCTTTTATTTTTA[-/TTTT]TTCTTTTAGGAAGCT | 8065 |
rs771092462 | snp | C/G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023311 | CTGCCTTTTCACTCC[C/G/T]TGAATGGTGTCTTTT | 8065 |
rs771111510 | snp | C/T | 0.00024635 | 0.0110957 | intron-variant | CUL5 | GRCh38.p7 | 11:108073377 | AACTTAATGTAAAAC[C/T]TTTTGTTTCTAGGAC | 8065 |
rs771143189 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047124 | AGAGTTTGATACCAG[C/T]CTGGGAAACATGGTG | 8065 |
rs771174018 | in-del | -/AATA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090190 | TAAACTGACCTTATT[-/AATA]AATAGACTACAGGGG | 8065 |
rs771190019 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026502 | ATCCTTGTACCAGCA[A/C]CTACATGTACATTCT | 8065 |
rs771221824 | snp | A/G | 9.03383e-05 | 0.00672019 | intron-variant | CUL5 | GRCh38.p7 | 11:108049854 | TTTTTCAAAGCAACT[A/G]CATTTATTTCAAATT | 8065 |
rs771246799 | snp | C/T | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104666 | AATTTGATTTGTACC[C/T]ACCAGGAGAAATACA | 8065 |
rs771248805 | in-del | -/TTAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067354 | TCTTCTCAGTTTACT[-/TTAA]TTATGTTGTCAATTT | 8065 |
rs771249822 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100714 | ATATTCGTAGCTATG[C/T]CAGGATAAACTCCTG | 8065 |
rs771315306 | snp | A/G | 8.64454e-05 | 0.00657383 | intron-variant | CUL5 | GRCh38.p7 | 11:108054619 | TTTTGATCATAATTG[A/G]AGTAATACTTTATTT | 8065 |
rs771355990 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060143 | TTATTAACCTTCAGT[A/G]TTTTGGTATTTCAGG | 8065 |
rs771406047 | snp | C/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106593 | CTACTTTTTGGTGTT[C/T]ATGAAAATCATTTAG | 8065 |
rs771474790 | snp | A/G | 1.70886e-05 | 0.00292301 | intron-variant | CUL5 | GRCh38.p7 | 11:108095035 | TCAGTTTGGATGAAA[A/G]TAGCAGGACTCCGCA | 8065 |
rs771482410 | snp | A/C | 1.65482e-05 | 0.00287643 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033818 | ATAAAGGTTCTCTTC[A/C]GTTTGAAGACAAATG | 8065 |
rs771498228 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092286 | GGTGCAGACACTTTG[G/T]AAAACTGTTGGGCAG | 8065 |
rs771504172 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057280 | CAGTTCTCCCACCTC[A/G]ACCTCCCAGAGTGCT | 8065 |
rs771513737 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015899 | GGATACTAGGCATCT[G/T]TCTAGTAAAAAGAGA | 8065 |
rs771539861 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108078369 | TGACTTTTGCAGCTT[G/T]TGGCTATTAAAGTTC | 8065 |
rs771559839 | snp | C/G/T | 3.32338e-05 | 0.00407627 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108052760 | AGAGATTGGGAGAAG[C/G/T]TTTTGATTCTCAGCT | 8065 |
rs771565506 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028129 | ATTTTCTGATAGGCC[A/T]TTTAAATTCTAGATT | 8065 |
rs771568513 | snp | C/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106944 | GTTTAAAGACAGAGA[C/T]ATCCCATCTGGAAAA | 8065 |
rs771570401 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063479 | GTTCCTTCCAAATCT[C/T]GATTATAAGTAGTGC | 8065 |
rs771594093 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108054855 | ATTCTTAAAATGATT[A/G]CTATTTTGCTTCTGG | 8065 |
rs771595182 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108074817 | GTCTCAAAAAATAAA[G/T]AAATAAAAATAAAAC | 8065 |
rs771618885 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028976 | AGTAAGCTAAGTTAC[A/T]TCTATGACCTTATCT | 8065 |
rs771645763 | snp | G/T | 1.64923e-05 | 0.00287156 | missense | CUL5 | GRCh38.p7 | 11:108088568 | CAAAATGCCCTGAGC[G/T]GCTTGCCAATTACTG | 8065 |
rs771646231 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061565 | CAGATTCAACAGTTA[C/T]CATTATTTTGTCATG | 8065 |
rs771663245 | snp | A/G | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105365 | ATCTGTAGCATAGAA[A/G]TATTTTGGTATTTTA | 8065 |
rs771667353 | in-del | -/TTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048649 | ATAGACTCCACCACC[-/TTTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 8065 |
rs771685531 | snp | G/T | 8.10816e-05 | 0.00636665 | intron-variant | CUL5 | GRCh38.p7 | 11:108104157 | AAATAATTTCGTATA[G/T]TAATGCGCTTTTATT | 8065 |
rs771696355 | in-del | -/CAAAAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040611 | AGTGAGACTCCGTCT[-/CAAAAA]AAAAAAAAAAAAAAA | 8065 |
rs771714382 | in-del | -/TT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058245 | ATTATGAAGAGTGCC[-/TT]TTTTTTTTTTTTTTT | 8065 |
rs771732053 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092721 | GGGGTTTCTTTTTGG[C/G]GTGATGAAAATGTTC | 8065 |
rs771739084 | in-del | -/TTTTTCTTTTAAA | 2.36273e-05 | 0.00343701 | intron-variant | CUL5 | GRCh38.p7 | 11:108073349 | TTTTTTGTGTTATTC[-/TTTTTCTTTTAAA]AACTTAATGTAAAAC | 8065 |
rs771742183 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029472 | GTAGCAAGTTAATAG[A/G]GATGAGGCAGCCTTC | 8065 |
rs771772598 | snp | A/G | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104892 | GCAACATTGGGAAAC[A/G]GCAGATGTAGGTGAG | 8065 |
rs771796079 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048016 | GCAAGAACCCAAGAA[G/T]GGGATTTAGCACCAC | 8065 |
rs771833226 | snp | C/T | 5.94301e-05 | 0.00545083 | intron-variant | CUL5 | GRCh38.p7 | 11:108055001 | GGATTATTTGAAATA[C/T]GGAAGCATAGGAATG | 8065 |
rs771844278 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039454 | CCTTCTAGGGGAACA[A/G]TACCTTCCTTAGTTG | 8065 |
rs771872973 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053249 | CTGGAGGCCTTTCTT[A/G]ATTCCCAGAGTAAGT | 8065 |
rs771876287 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100500 | AGTGAGCCTAGATTG[C/T]GCCACTGCACTCCAG | 8065 |
rs771879927 | snp | A/G | 1.66877e-05 | 0.00288852 | missense, intron-variant | CUL5 | GRCh38.p7 | 11:108104364 | GAATCTGATATCAAC[A/G]CTTTCATATATATGG | 8065 |
rs771898749 | in-del | -/TTT | 4.68044e-05 | 0.00483736 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033787 | AAACTCCCTTTTATC[-/TTT]TTTTTTTTCAAGAAT | 8065 |
rs771927062 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012514 | GACTTGGTGGTATGT[-/C]CCCTCTTACTTTTTT | 8065 |
rs771987785 | snp | C/G/T | 3.39583e-05 | 0.00412046 | intron-variant | CUL5 | GRCh38.p7 | 11:108009404 | AGCTTGGGTTTTACT[C/G/T]TGTGGCCGCCGGGTT | 8065 |
rs772029658 | snp | A/C | 3.35616e-05 | 0.0040963 | intron-variant | CUL5 | GRCh38.p7 | 11:108070237 | CTTCTAAGAGGGTAT[A/C]TTTGAAACAAATCAC | 8065 |
rs772033793 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086206 | TAAATACAAATTAAA[A/C]CATTCCTAGGTACAT | 8065 |
rs772034997 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009868 | GTGCCTCCCACTCCA[A/C]CCCCCTTCCTCCCTT | 8065 |
rs772118032 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019962 | AGAGAGTGGGGAGAG[G/T]TACCAGGCTCTTTTT | 8065 |
rs772158269 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108045328 | AAAGACAAAATAGGC[G/T]GGCCCACAATCCCAC | 8065 |
rs772182050 | snp | A/G | 9.9519e-05 | 0.00705334 | missense | CUL5 | GRCh38.p7 | 11:108078203 | GTTGTTAATGATGCT[A/G]CCATATTTAAACTTG | 8065 |
rs772268465 | snp | G/T | 1.69539e-05 | 0.00291147 | intron-variant | CUL5 | GRCh38.p7 | 11:108049881 | AATTGGTACACCTCT[G/T]TTTTTCAGCGAGTAC | 8065 |
rs772269107 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070422 | AACATCTGTGTATGT[A/G]TATGGTGAATTTCTA | 8065 |
rs772269749 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032359 | AAAAAAATACAACAA[C/T]TAGCTGGGCATGGTG | 8065 |
rs772306284 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069962 | ATCTTCAATAATCCT[A/G]TAGTTAAGGTAAGTG | 8065 |
rs772395362 | snp | A/G | 2.40503e-05 | 0.00346765 | intron-variant | CUL5 | GRCh38.p7 | 11:108073516 | TATATTCCTATATAT[A/G]TAAAAAACACTTTTA | 8065 |
rs772395801 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060764 | ATCGCTTGAACCCGG[C/G]AGGCGGAGGTTGCAG | 8065 |
rs772400422 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085330 | AAGCCAGACACATAA[A/G]GACAAATTTTGCATG | 8065 |
rs772435876 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071814 | CCACCTTGGCCTCCC[-/A]AAGTGCTGGAGTTAC | 8065 |
rs772467577 | snp | C/T | 1.71082e-05 | 0.00292469 | intron-variant | CUL5 | GRCh38.p7 | 11:108050090 | ATTTTTCTCCTTGTT[C/T]TCCTAATATTCTTCA | 8065 |
rs772484778 | snp | C/T | 1.64885e-05 | 0.00287123 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108097707 | CAACTCACCCAAAGA[C/T]TTTACAGAAGGTACC | 8065 |
rs772520793 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068211 | GCTATGAGCCACCAC[A/G]CCCAGCCATGTGTAT | 8065 |
rs772521624 | snp | A/G | | | missense, intron-variant | CUL5 | GRCh38.p7 | 11:108104358 | AGAGATGAATCTGAT[A/G]TCAACACTTTCATAT | 8065 |
rs772559024 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024195 | GATTTCCTGCCCTGC[C/T]ACTTACTGCCTATAA | 8065 |
rs772560813 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036856 | AACACATTACAGCTG[C/T]TGGGAAATCCTGACT | 8065 |
rs772594222 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013709 | ATGATTCATACTACT[G/T]TTCTCAGTGGACTTT | 8065 |
rs772611899 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025328 | TTTCCTGTTTCTTTG[A/C]ATGCTTGGTAGTTTT | 8065 |
rs772621396 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059247 | CCTGCATACCTTAGT[A/G]TTTCCTGGGGAAATT | 8065 |
rs772636247 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092758 | TAGATAGTGGTGATG[A/G]TTGCACAGTTCTGTA | 8065 |
rs772675013 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068268 | GGATATATGCATTTA[A/G]AAGTCATCAGCATCA | 8065 |
rs772792254 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026528 | ATTCTTTTGCCTTCT[C/T]CTCTTAGCCTGTAGT | 8065 |
rs772823708 | snp | A/G | 1.65023e-05 | 0.00287244 | missense | CUL5 | GRCh38.p7 | 11:108097739 | TCTTCTCAGTGAACC[A/G]GGAGTTCAGTTTAAT | 8065 |
rs772850189 | in-del | -/AAG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018770 | CACTTTTGTTGAGAT[-/AAG]AAAGATTTTATGAAT | 8065 |
rs772864814 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009927 | TCTCCCATTCTTGAG[C/T]TCATCTTTTTCCTTA | 8065 |
rs772885787 | snp | A/G | | | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108107772 | TAAAAGCTTTTACCT[A/G]TCCAGAAAATGTTGA | 8065 |
rs772886015 | snp | A/G | 1.66297e-05 | 0.0028835 | intron-variant | CUL5 | GRCh38.p7 | 11:108054816 | GAACTTAGTATATGT[A/G]ATAATTTGAGCAATT | 8065 |
rs772905554 | snp | A/G | | | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094471 | TGAAGATTTGAACCA[A/G]GCTTTTAAGGAAATG | 8065 |
rs772920398 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081738 | GCCTGGGTGAGAGTG[C/T]GAGTCTCCGTCTCAA | 8065 |
rs772981040 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023787 | TATTTGTTTGGGTTT[-/C]AAAAAATACAAGTAT | 8065 |
rs772988050 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076990 | ATCCATATGGTAATG[-/T]TGAGTCTGGAGCTTA | 8065 |
rs772997686 | in-del | -/AAAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100151 | GAAACTTAAAAAAAT[-/AAAA]AAAAGGTGGTAGTGG | 8065 |
rs773003159 | snp | C/G/T | 3.39849e-05 | 0.00412207 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009326 | ATTCTCGCGTCGTCT[C/G/T]GCGAGAGTCCAAGTT | 8065 |
rs773006047 | snp | A/G | 1.6599e-05 | 0.00288084 | intron-variant | CUL5 | GRCh38.p7 | 11:108089458 | AGATGGTAAGAGTAT[A/G]TAAGAACTGAAAGTA | 8065 |
rs773021944 | snp | A/G | 2.14991e-05 | 0.00327858 | intron-variant | CUL5 | GRCh38.p7 | 11:108089644 | TAAATTTTTTTAAAT[A/G]TTTGGTTTTCTAATA | 8065 |
rs773045827 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108049725 | TAATGCTGCTGTGAA[C/T]ATTCGTGTACAAGTT | 8065 |
rs773074880 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079646 | CATAAATCTTAAGTG[C/T]ACATTTGAGTCAGAT | 8065 |
rs773089611 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024592 | ATTTACACATCTACG[-/C]CTGAAGATTATAGTG | 8065 |
rs773093825 | snp | A/G | 1.73273e-05 | 0.00294335 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104409 | TCATGGACAATATTT[A/G]GAACCCAAATTTTGG | 8065 |
rs773108246 | snp | A/G | 1.71211e-05 | 0.00292579 | intron-variant | CUL5 | GRCh38.p7 | 11:108033962 | GGAAATTTTAGTGAT[A/G]TCTTTCCATACCCAA | 8065 |
rs773147292 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031697 | GGTTACTACAGTGCT[-/G]TCGTATAAAGACACA | 8065 |
rs773174060 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028227 | CTAAAACCAGTCTCA[C/G]AAGCTTTCCTTAATA | 8065 |
rs773194252 | snp | A/G | | | intron-variant, utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108074048 | ATCTTTTTTAGTGTA[A/G]TAAACCTATAACAAG | 8065 |
rs773235593 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031393 | AAATCATGAGTTTCA[A/T]AGGGTGTTTGGTGCT | 8065 |
rs773265157 | snp | A/G | 1.64817e-05 | 0.00287064 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054675 | TAATCCTGAGGATAA[A/G]CTTCAAATTTATAGG | 8065 |
rs773302035 | snp | A/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107029 | TAAGAAGTAAAAATA[A/T]AGAAAAATTTTGATG | 8065 |
rs773302243 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033869 | TTTTGAAGCTTTTAC[A/G]CCAGGAATCTGTTAC | 8065 |
rs773359398 | in-del | -/TTTTA | 5.85337e-05 | 0.00540957 | intron-variant | CUL5 | GRCh38.p7 | 11:108104166 | CGTATATTAATGCGC[-/TTTTA]TTTTTATTTTTTCTT | 8065 |
rs773359469 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053374 | TAGAATGCATGGCAC[A/C]AAATCACTCTAGGTA | 8065 |
rs773360875 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098294 | CATTTAACCTTTAAA[C/T]AGTTCTGATATTTTA | 8065 |
rs773371784 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108021359 | AATTCTATGGATGCC[A/G]TTATTTCTTGCTCTT | 8065 |
rs773373454 | snp | A/G | | | missense | CUL5 | GRCh38.p7 | 11:108078182 | TTTTTGCAGGCGTAT[A/G]AAGCAGTTGTTAATG | 8065 |
rs773451084 | snp | G/T | 1.69986e-05 | 0.0029153 | intron-variant | CUL5 | GRCh38.p7 | 11:108095024 | TATTTCAGCTTTCAG[G/T]TTGGATGAAAGTAGC | 8065 |
rs773454555 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084596 | CTTGTGTGATTCTTA[C/T]ATATACAGTGTCCAG | 8065 |
rs773488535 | snp | C/G | 1.65304e-05 | 0.00287488 | missense | CUL5 | GRCh38.p7 | 11:108088543 | GTGGGATTAAAAACT[C/G]AGCCTGAATCAAAAT | 8065 |
rs773488713 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103185 | TTCTGATAACTCTTA[C/T]TGTAAACTTAACAGT | 8065 |
rs773514285 | snp | A/G | 3.31406e-05 | 0.00407053 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108052726 | CTCCAAGATAGTGCA[A/G]TGAAGCTGGTACATG | 8065 |
rs773524882 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033294 | GATGGAGCTTATTCA[C/T]ATAGGTGTGATTGAT | 8065 |
rs773530742 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063267 | TTCAATTGTTTTAAT[G/T]TTTAGCTTCCACAAA | 8065 |
rs773545415 | in-del | -/TATA | 8.30351e-05 | 0.00644288 | intron-variant | CUL5 | GRCh38.p7 | 11:108089455 | GAGAGATGGTAAGAG[-/TATA]TAAGAACTGAAAGTA | 8065 |
rs773552305 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008760 | CATTTCAGGACAATG[C/T]ACCTCCCTTAACACC | 8065 |
rs773561810 | snp | A/G | 3.97038e-05 | 0.00445537 | intron-variant | CUL5 | GRCh38.p7 | 11:108073372 | TTAAAAACTTAATGT[A/G]AAACCTTTTGTTTCT | 8065 |
rs773576181 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089258 | ATTTTATACAAAATC[G/T]AAAAAACTGATATTT | 8065 |
rs773606113 | snp | A/C | 1.73872e-05 | 0.00294844 | intron-variant | CUL5 | GRCh38.p7 | 11:108050111 | ATATTCTTCAGAAAG[A/C]GGGTAATTTGGAAGC | 8065 |
rs773615563 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070452 | ACTTTTTTCTCAAAA[A/G]CAAGACACTGCTTTT | 8065 |
rs773620625 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060770 | TGAACCCGGGAGGCG[C/G]AGGTTGCAGTGAGAT | 8065 |
rs773659891 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025329 | TTCCTGTTTCTTTGC[A/G]TGCTTGGTAGTTTTT | 8065 |
rs773684826 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108073714 | GAATTTAGTTAGAAA[A/G]TTGCTTTTTTCTCAT | 8065 |
rs773702013 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042511 | GCAAGCTTGAGCCAC[G/T]GCACCTGGCCCACAA | 8065 |
rs773713806 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083105 | TTCTTTTCTCTGACT[A/G]ATTGCTCTGACCGGA | 8065 |
rs773719154 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013767 | GGAAATGTAAAGCAG[G/T]GATTCAGAGTGTCTA | 8065 |
rs773735999 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014962 | GGAGTGCAGTGGCAC[A/G]ATCTTGGCTCACTGC | 8065 |
rs773747233 | snp | A/C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015678 | AATAGTGGACTAATC[A/C/G]GTAACTGTAAAACTT | 8065 |
rs773767741 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052585 | CAAATTTGATTTCCT[G/T]TTTTGGTGTTTGTAC | 8065 |
rs773768416 | snp | A/G | 1.65151e-05 | 0.00287355 | missense | CUL5 | GRCh38.p7 | 11:108097748 | TGAACCAGGAGTTCA[A/G]TTTAATGTAAGCTCG | 8065 |
rs773780799 | snp | G/T | 1.69232e-05 | 0.00290883 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009331 | CGCGTCGTCTCGCGA[G/T]AGTCCAAGTTAAAGA | 8065 |
rs773804042 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026635 | TCCCTTTCCCCACAT[A/C]ATCAACATTTCATAT | 8065 |
rs773807998 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043977 | GCAGTGAGCCAAGGT[A/G]GCGCCATTGCACTTC | 8065 |
rs773815383 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093821 | CCCACCTCAGCCTTC[C/T]GAGTAGCTGGGACTA | 8065 |
rs773825624 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026292 | TTTGCACCTTAAATC[C/T]ATGACCACAATGAGG | 8065 |
rs773827272 | snp | A/G | 1.65559e-05 | 0.00287709 | missense | CUL5 | GRCh38.p7 | 11:108094871 | AGAAGTTCTGAGAAA[A/G]TCTTTGTCTCACTTC | 8065 |
rs773855017 | snp | G/T | 1.65288e-05 | 0.00287474 | intron-variant | CUL5 | GRCh38.p7 | 11:108098538 | AACCCAGGTTTGTAA[G/T]GTTGACAGAATGTCT | 8065 |
rs773855606 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027981 | TAGTTCTTACTCCTC[C/T]CTCCGCCTCTTAATG | 8065 |
rs773857815 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076909 | AGAAATAGTTTTTGG[A/C]GAGATGGTTGCAGAG | 8065 |
rs773873220 | snp | G/T | 3.38278e-05 | 0.00411251 | intron-variant | CUL5 | GRCh38.p7 | 11:108009395 | CCTCACTCCAGCTTG[G/T]GTTTTACTGTGTGGC | 8065 |
rs773884177 | in-del | -/TC | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032583 | AACACATATGGGGTC[-/TC]TCTCTCTCTCTCTCT | 8065 |
rs773941745 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059456 | ACCGATAGGGAGGGA[A/G]TGTATTACAGTGGTT | 8065 |
rs773950528 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052006 | GCTCTTGCTGTGTTG[C/T]CCAGGCTAGAGTGGA | 8065 |
rs774024700 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092607 | TCCCAAAGACCATAT[C/T]GTATGATTCCACTAA | 8065 |
rs774038315 | snp | A/G | 3.32403e-05 | 0.00407664 | intron-variant | CUL5 | GRCh38.p7 | 11:108078260 | GTTTTTTAAAACCAT[A/G]CTTTAAAAATACTTA | 8065 |
rs774111171 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016259 | TCTCTTCTCGTCTTC[C/T]CTTCTCTTCTCTTTT | 8065 |
rs774131781 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066033 | ACTTTTATTGTTTTA[C/T]TTTTCTATTCAAAAA | 8065 |
rs774137907 | snp | C/G | 1.6628e-05 | 0.00288335 | intron-variant | CUL5 | GRCh38.p7 | 11:108054833 | TAATTTGAGCAATTC[C/G]CTTGATATTCTTAAA | 8065 |
rs774143430 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060364 | CCTGATAATGATAGA[A/G]TAGAATCATAAAGTG | 8065 |
rs774150726 | snp | A/G | 1.84401e-05 | 0.0030364 | intron-variant | CUL5 | GRCh38.p7 | 11:108054983 | GTAATTGTACATTTT[A/G]TGGGATTATTTGAAA | 8065 |
rs774155348 | snp | C/T | 5.28416e-05 | 0.00513984 | intron-variant | CUL5 | GRCh38.p7 | 11:108089674 | ACATTACATCATTTA[C/T]ATGTGTGCTTAAGTA | 8065 |
rs774158757 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085140 | AATGTTCATAGTAGA[A/G]TGGCATTACTCTTAA | 8065 |
rs774190508 | snp | A/G | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104835 | TTAAAACTAGAAATA[A/G]CACTCTTGGTTTCTT | 8065 |
rs774294553 | snp | C/T | | | synonymous-codon, intron-variant | CUL5 | GRCh38.p7 | 11:108104348 | ATACATCAGAAGAGA[C/T]GAATCTGATATCAAC | 8065 |
rs774298390 | snp | A/G | | | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074121 | ACTTCCCAAGTTTGA[A/G]TGATTCTAAAAAGAC | 8065 |
rs774299421 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035916 | TTTCAGGATTCCAAA[A/G]CAGTTAGTGTCTTGT | 8065 |
rs774425148 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015586 | TGTCCTAGAGAGATG[A/G]TTGCATTCGACACAG | 8065 |
rs774493759 | in-del | -/CAAAAAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040611 | AGTGAGACTCCGTCT[-/CAAAAAA]AAAAAAAAAAAAAAA | 8065 |
rs774504928 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030428 | AGATCACCTGAGGTC[C/G]GGAGTTTGAGACCAG | 8065 |
rs774521738 | snp | C/T | 3.23787e-05 | 0.00402347 | intron-variant | CUL5 | GRCh38.p7 | 11:108095487 | ATATTAAGAGAGAAT[C/T]ATCATGAGATTCTTT | 8065 |
rs774524518 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108046223 | AAGATGTTTTGTTCA[A/G]TTCTTGTTTCATTAT | 8065 |
rs774570894 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065759 | AGTTAAAACCAGGTA[C/T]TATGAGTGCCCACCT | 8065 |
rs774581956 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108097043 | TTTTTGTTGAGACAG[A/T]GTCTTGCTCTGTCCT | 8065 |
rs774591420 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024139 | ACCAGAGAATAGTTA[A/G]TTAAGAATGTGGCTT | 8065 |
rs774607853 | in-del | -/AAC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014373 | CCCAGAATACAGGGA[-/AAC]AACAAGAGGGATAGG | 8065 |
rs774613995 | snp | C/T | 5.12492e-05 | 0.00506182 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108073404 | GGACTCTGAGAAATA[C/T]GTTGAGCAGTTACTT | 8065 |
rs774620515 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076000 | TAGCATGAATCCAAT[A/G]TACAGTATAATTTGA | 8065 |
rs774622165 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088992 | ACTCCTTCCTTTTTG[C/T]GAGAGTCCAAGATAG | 8065 |
rs774643174 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069076 | CCTGGGGAACATAGC[A/C]AGACATCATCTCTAC | 8065 |
rs774660542 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102291 | CCTTGGCCTCCTAAA[A/G]TGCTGGGATTACAGG | 8065 |
rs774703100 | in-del | -/GTATGATAGCTTCCTAA/GTATGATAGCTTCCTAAA | 5.17481e-05 | 0.00508643 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104408 | TCATGGACAATATTT[lengthTooLong]AGAACCCAAATTTTG | 8065 |
rs774729696 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023232 | CCAGCCTGGGCAACA[A/G]ACAAAACTCTGTATC | 8065 |
rs774776784 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096116 | AAAAAAAAAATTATG[C/T]ACACACACACACACA | 8065 |
rs774792422 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053173 | GGAGTACATTCTCTC[-/T]TACTTCTAATTTGTT | 8065 |
rs774890602 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057935 | AAGAATATTGGCTGG[G/T]TGCAGTGGCTCACGC | 8065 |
rs774893870 | snp | A/T | 1.69562e-05 | 0.00291167 | intron-variant | CUL5 | GRCh38.p7 | 11:108088478 | TTAGAAAAAAATAAT[A/T]GCAAACATTAATCAT | 8065 |
rs774917545 | snp | A/G | 4.94539e-05 | 0.00497238 | missense | CUL5 | GRCh38.p7 | 11:108095657 | TTAAGCTTGCAACTG[A/G]ACTCCCTGATGCTGA | 8065 |
rs774986079 | snp | C/T | 1.67203e-05 | 0.00289134 | intron-variant | CUL5 | GRCh38.p7 | 11:108072475 | ACTGTAAGTTTTTTT[C/T]CAATGGCAATGATAG | 8065 |
rs774990011 | snp | C/T | 5.75777e-05 | 0.00536522 | intron-variant | CUL5 | GRCh38.p7 | 11:108088697 | AACTTTTAAAATTAC[C/T]TTACTTTGAATTTGT | 8065 |
rs775007674 | snp | A/C | 3.29886e-05 | 0.00406118 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108088596 | CTGTGACATGTTGCT[A/C]AGAAAAACACCATTA | 8065 |
rs775027187 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087750 | CAGGTGGATCACCTG[A/G]GGTCAGAAGTTTGAG | 8065 |
rs775058357 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103290 | AAGTGACTGGGCATC[A/G]TGGCTTACACCTGTA | 8065 |
rs775058761 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108073573 | TAATAATCAATTTGC[A/G]TTATTTTTCTATTAA | 8065 |
rs775064658 | in-del | -/CA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096117 | AAAAAAAATTATGCA[-/CA]CACACACACACACAC | 8065 |
rs775148151 | snp | A/G | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104875 | AGAGTGAGCTGGTCA[A/G]TGCAACATTGGGAAA | 8065 |
rs775160152 | snp | C/T | 3.96369e-05 | 0.00445162 | intron-variant | CUL5 | GRCh38.p7 | 11:108104163 | TTTCGTATATTAATG[C/T]GCTTTTATTTTTATT | 8065 |
rs775190854 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070499 | TGGAAACATATGTTA[C/T]AGATTAGAACCAGGT | 8065 |
rs775219742 | snp | C/G | 1.68306e-05 | 0.00290087 | intron-variant | CUL5 | GRCh38.p7 | 11:108070241 | TAAGAGGGTATCTTT[C/G]AAACAAATCACTTAC | 8065 |
rs775231351 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042148 | CTTCACATTTTCACA[-/T]TTTTACTTTACAGGG | 8065 |
rs775240160 | in-del | -/GTTTC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098053 | TTTTTGTGTTGTTTT[-/GTTTC]GTTTTTGTTTTTGTT | 8065 |
rs775279055 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071716 | CACACCCAGCTAATT[C/T]TGTTTGTTTGTTTTT | 8065 |
rs775306826 | snp | A/T | 1.68394e-05 | 0.00290162 | utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108009341 | CGCGAGAGTCCAAGT[A/T]AAAGAACATGGCGAC | 8065 |
rs775333266 | in-del | -/GA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061895 | CTTATGTGGCAGCAG[-/GA]GAGAGAGAGAGAGAG | 8065 |
rs775387877 | in-del | -/C | 0.000134802 | 0.00820869 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033797 | TATCTTTTTTTTTTT[-/C]CAAGAATAAAGGTTC | 8065 |
rs775395061 | snp | A/T | 1.71056e-05 | 0.00292446 | intron-variant | CUL5 | GRCh38.p7 | 11:108050091 | TTTTTCTCCTTGTTT[A/T]CCTAATATTCTTCAG | 8065 |
rs775400895 | snp | A/C | 1.68391e-05 | 0.0029016 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094819 | CTCTATAGCTGATTC[A/C]GTTAATATAAAAATT | 8065 |
rs775415971 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060573 | GGATGCCGTGGCCCA[C/T]GCCTCTAATCCCAGC | 8065 |
rs775421553 | in-del | -/GC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039304 | GGATTACAGGCATGA[-/GC]CACTGTGCCCGGCCT | 8065 |
rs775562603 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087596 | GAGACCTTGTCTGAA[A/T]TTAAAAAATTTTTTA | 8065 |
rs775574426 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056197 | AGAATCTAGTTGGGA[C/T]AGTCTTGGAATTGTT | 8065 |
rs775575991 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012363 | CATTACTTTACCCAG[A/C]TATTTGAAGTGCCCT | 8065 |
rs775603964 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083125 | CTCTGACCGGAACGT[C/T]TACTACAGTAACAAA | 8065 |
rs775618010 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041980 | ATACATGTTACTTTT[A/G]TTATAGTAAACTAAA | 8065 |
rs775619759 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012983 | AGCCCCCATTTGCTG[C/G]CTTTATAATTCTTTG | 8065 |
rs775638217 | in-del | -/AAC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017545 | TAGGGCGGTAGCGAA[-/AAC]AACGTGATAAGAATG | 8065 |
rs775660861 | snp | A/G | 1.68119e-05 | 0.00289926 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108073425 | GCAGTTACTTACACT[A/G]TTTAATAGATTTAGT | 8065 |
rs775680501 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086533 | GCCAGGCATTGCAAG[A/G]AGAGATGGATGGATT | 8065 |
rs775684212 | snp | C/T | 2.88996e-05 | 0.00380118 | intron-variant | CUL5 | GRCh38.p7 | 11:108094521 | CATTACCAGGTATTA[C/T]TTTATAATTACATGT | 8065 |
rs775692877 | snp | A/G | 3.34448e-05 | 0.00408917 | missense, intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108049891 | CCTCTTTTTTTCAGC[A/G]AGTACTGAGCCATCA | 8065 |
rs775734481 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034102 | CAGGACTGAACATAC[A/G]ATCATACTCACAGCT | 8065 |
rs775757181 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102139 | TGATTCTCCTGCCTC[A/G]GACTCCTGAGTAGCT | 8065 |
rs775762148 | snp | C/T | 1.64893e-05 | 0.0028713 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108097710 | CTCACCCAAAGACTT[C/T]ACAGAAGGTACCCTC | 8065 |
rs775800521 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090831 | TATTTTAACTTATAG[C/G]TAGCCCTTCGCATGG | 8065 |
rs775828565 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067891 | AAGGAAAGAGTTTCT[C/T]AACCATTTTATATGT | 8065 |
rs775881726 | snp | C/G | | | intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108055391 | TCATTTATTCCTAGG[C/G]GATATTTCTTCTCCT | 8065 |
rs775888952 | snp | A/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033084 | TAGTTATGATTTGTT[A/T]TAGGGAAAGGATTCA | 8065 |
rs775898488 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029602 | CCTGCCACTTAGTTA[C/T]GATTTAATGATATGC | 8065 |
rs775932640 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108050164 | TAAGTGGGTTTTTCT[A/G]CTTCACATGTCAATT | 8065 |
rs775940158 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022021 | ATCCATCGATCCATC[C/T]ATTCTTAGAGATGGG | 8065 |
rs775957554 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047832 | AAGATAAATTATGTT[C/T]ATTTCAGATAGATAG | 8065 |
rs775970568 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081463 | TCCATTATCAAAAAT[C/T]GGTTGGCTGCCAGGC | 8065 |
rs775985935 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018368 | CAACCAACCAAAGAT[C/T]AAAAATACTCAGAAA | 8065 |
rs775994910 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093349 | TAGCATTTTTGCCAG[C/G]ATCACTTCTTCTAGG | 8065 |
rs776120537 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069223 | GATAGTAGCTATGTA[A/G]TAATGCCACTGTACT | 8065 |
rs776137420 | snp | A/T | 1.67939e-05 | 0.0028977 | intron-variant | CUL5 | GRCh38.p7 | 11:108046232 | TGTTCAGTTCTTGTT[A/T]CATTATTAATGTTTG | 8065 |
rs776173464 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099715 | TGTGTCACACCAGTC[A/G]TCTTCCCATGTTTCC | 8065 |
rs776236248 | snp | A/C/G | 3.49872e-05 | 0.00418242 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054656 | TTTCAGTTAACCTTT[A/C/G]TTCTAATCCTGAGGA | 8065 |
rs776245969 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028485 | CCCAGTTTTAACCCT[A/T]GCCCCTTATAATATA | 8065 |
rs776271860 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010133 | AAGTTTGGAGAAGAA[C/T]GAGGAAGACTTAGAA | 8065 |
rs776277107 | in-del | -/ATAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068515 | TGTAGGAAGAACAGT[-/ATAA]TGAATCCCCATTACC | 8065 |
rs776328098 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096669 | CCTCCAGGGTTTAAG[C/T]GATTCTCCTACCTCA | 8065 |
rs776357518 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108044772 | TAATTTATTATTATT[A/T]TTTTTTTGAGACACA | 8065 |
rs776358493 | snp | A/G | 0.000115461 | 0.00759718 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033845 | AATGGGATTTTATGC[A/G]CCCGATTGTTTTGAA | 8065 |
rs776364950 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102337 | CCGGCCTATTTTTCT[A/G]TTCTTTTGAGACAGG | 8065 |
rs776378518 | in-del | -/TTTG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023811 | CAAGTATTGCTAGAA[-/TTTG]TTTGAAATTTTTTTC | 8065 |
rs776381486 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036913 | CAGGCAGCAGCAGCT[A/C]GTCTGAAGAAACAGC | 8065 |
rs776413028 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082925 | AGCTACCATGCCCAA[C/T]CACAAATAATTTTTA | 8065 |
rs776425758 | snp | A/T | 5.13545e-05 | 0.00506701 | synonymous-codon, intron-variant | CUL5 | GRCh38.p7 | 11:108104195 | TTTCTTTTAGGAAGC[A/T]ATCATACAAATAATG | 8065 |
rs776430763 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096097 | TGAGAACTCCGTCTG[-/A]AAAAAAAAAAAAATT | 8065 |
rs776431315 | snp | A/T | 1.66158e-05 | 0.0028823 | intron-variant | CUL5 | GRCh38.p7 | 11:108054796 | TATATGAAATATGTA[A/T]GTTAGAACTTAGTAT | 8065 |
rs776445530 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070641 | TTTTTTATTACTTCA[A/G]TGTTTTCTTAAAAAG | 8065 |
rs776461873 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024196 | ATTTCCTGCCCTGCC[A/G]CTTACTGCCTATAAT | 8065 |
rs776462900 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075113 | AATACCAGTTAAGAA[C/G]TTATTTAAATAATTC | 8065 |
rs776479570 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057874 | GTGAGGTGCTATTTT[C/T]CTGCTAACTTTTCTG | 8065 |
rs776493893 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029321 | TGTAAGGAGTGAAGG[A/T]TAGAGGGGCAGGAGT | 8065 |
rs776503494 | snp | G/T | 1.66101e-05 | 0.0028818 | missense | CUL5 | GRCh38.p7 | 11:108094847 | ATTCTGAATGCTGGC[G/T]CCTGGTCAAGAAGTT | 8065 |
rs776505433 | in-del | -/T | 1.65562e-05 | 0.00287712 | frameshift-variant, intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108049919 | TCAAGATGATACGGC[-/T]TTGCTAAAAGCATAT | 8065 |
rs776512532 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030171 | CAAAGTATATGCCGC[A/G]GCATCACAATTCTGA | 8065 |
rs776523480 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040711 | GATCCTTGAGCACAG[G/T]AGTTTTAAGTTACGA | 8065 |
rs776525007 | snp | A/T | 1.64958e-05 | 0.00287187 | missense | CUL5 | GRCh38.p7 | 11:108072388 | GGTATAGAGCCAATG[A/T]TGAAAGACTTGGAGG | 8065 |
rs776548472 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075936 | CTGACATAGTTACTC[A/G]TTTTCTTGTTTTGTT | 8065 |
rs776552531 | in-del | -/TTG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098084 | TGTTTTTGTTTTTGT[-/TTG]TTAAGACCCAGTTAG | 8065 |
rs776569141 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063801 | GTATTAGTTTTTTGA[A/G]GAACCTCCAAACTGC | 8065 |
rs776573935 | snp | C/T | | | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108108120 | AAAGTAAAAAATGGG[C/T]CGGGCTCAGTGGCTC | 8065 |
rs776633825 | snp | A/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107146 | CATTTATTGGAGGGG[A/T]CCCTGAGTTCTGTCA | 8065 |
rs776661445 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100727 | TGCCAGGATAAACTC[C/T]TGGAGTAAAGAGTTG | 8065 |
rs776684975 | in-del | -/T | 1.69117e-05 | 0.00290785 | intron-variant | CUL5 | GRCh38.p7 | 11:108088492 | TGCAAACATTAATCA[-/T]TTTTTCCATCAACTG | 8065 |
rs776701436 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022908 | ATGGACTTTTTAGTT[C/T]TTTACATATTCTGGA | 8065 |
rs776702711 | snp | A/C | 1.65285e-05 | 0.00287471 | missense | CUL5 | GRCh38.p7 | 11:108088625 | TAAGCAAAAAACTAA[A/C]CTCTGAAGAGATTGA | 8065 |
rs776737839 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096328 | TGCAATCCCATCTCT[-/A]AAAAAAAAAAAAAAA | 8065 |
rs776751376 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086439 | CAAAACAAAAATAAA[A/G]ACTGATAGCTGTCCT | 8065 |
rs776767648 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036652 | CAGGCTAATTTTTGT[A/G]TTTTCATTAGAGACA | 8065 |
rs776771898 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011268 | CTTTGGTCTATATTA[C/G]TTAAGTACTTACCTG | 8065 |
rs776780851 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010023 | CCATCGTTTTAGGGC[G/T]CAGGAAAGTTACCTT | 8065 |
rs776791251 | snp | A/G/T | 6.61791e-05 | 0.00575197 | intron-variant | CUL5 | GRCh38.p7 | 11:108094539 | TATAATTACATGTAT[A/G/T]TATTTTTTAAACTTA | 8065 |
rs776809632 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100031 | ATTGGTTTTTCTGAT[A/G]TTAATATCAAGTTCA | 8065 |
rs776859012 | snp | A/C | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105196 | CAGAGCCAAAATAGC[A/C]AAACAAACATATTAA | 8065 |
rs776895933 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085474 | AAGATTTCTGTTTGG[A/G]ATAATGAAGAAGTTC | 8065 |
rs776911073 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108071520 | GACCTTTTAAAGAAA[C/G]GAGTTGGGTTTTGCA | 8065 |
rs776919020 | snp | A/G | 4.97822e-05 | 0.00498885 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108078238 | ACCTTTGAAGCAGAA[A/G]GGGTAAGTTTTTTAA | 8065 |
rs776954719 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009755 | CATCAAAGGAAAAAC[C/T]AAGAAAATGCTGCCT | 8065 |
rs776988896 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108045687 | GACAACATAGCAAGA[C/T]TGTTTCTACAACAAA | 8065 |
rs776993026 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108078440 | TGACTTTATTTTTTC[A/C]GGTAAAAAAAAAATA | 8065 |
rs777006695 | snp | A/G | 1.64993e-05 | 0.00287218 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108098430 | AAAGGTTCAGAAAAG[A/G]GGTAAAATCAACTTG | 8065 |
rs777006777 | snp | A/T | 1.77253e-05 | 0.00297697 | intron-variant | CUL5 | GRCh38.p7 | 11:108073542 | TTTTAAAAGTTTTAT[A/T]CTCATAATTTACTTC | 8065 |
rs777038354 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039891 | AGTTTATTTCCATTA[A/G]TGGTTGCCTTCGTGT | 8065 |
rs777070757 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079428 | TTTTTTTAATGAAAA[-/T]TGTTCAAACTTACAA | 8065 |
rs777097073 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029019 | TTGTTTACTTTGCTC[G/T]ACCTTGAATACATTA | 8065 |
rs777109197 | in-del | -/CCTCACT | 3.36395e-05 | 0.00410105 | intron-variant | CUL5 | GRCh38.p7 | 11:108009380 | TGTTAAAGGTAAGAC[-/CCTCACT]CCAGCTTGGGTTTTA | 8065 |
rs777109937 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014798 | AGAGACAATAAACAT[A/G]AACAGTGAAATACAT | 8065 |
rs777124261 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047232 | TGAGGCAGGAGAATT[A/G]TGTGAGCCTGGAAGA | 8065 |
rs777132097 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083852 | AGGTGGTGTGGCTAT[G/T]GGAGGTGTGGAGGAG | 8065 |
rs777160115 | snp | C/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032603 | TCTCTCTCTCTCTCT[C/G]TTTTTGGCAATGTAA | 8065 |
rs777186311 | snp | A/G | 5.16249e-05 | 0.00508033 | intron-variant | CUL5 | GRCh38.p7 | 11:108050098 | CCTTGTTTTCCTAAT[A/G]TTCTTCAGAAAGAGG | 8065 |
rs777284221 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041651 | GCTGGAGTGCAGTAG[C/T]GTGATCTCGGCTCAC | 8065 |
rs777288052 | snp | G/T | 1.73309e-05 | 0.00294366 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054953 | TGTAACTCCGTTGAA[G/T]CAGTAAGTAATTTTG | 8065 |
rs777295313 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096011 | TGAGGCAGGAGAATC[A/G]CTTGAATTCAGGAGG | 8065 |
rs777295327 | snp | A/C | 3.29745e-05 | 0.00406031 | missense | CUL5 | GRCh38.p7 | 11:108070160 | TCTTAGCTGAGTGCC[A/C]AGGCATGATCAAGAG | 8065 |
rs777378519 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076520 | TTTTAGGTTCTACCT[A/G]TAAGTGAGATCATGC | 8065 |
rs777393996 | snp | C/T | 1.71879e-05 | 0.00293149 | stop-gained | CUL5 | GRCh38.p7 | 11:108094469 | TCTGAAGATTTGAAC[C/T]AAGCTTTTAAGGAAA | 8065 |
rs777441480 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059704 | CAACACGGTGAAACC[C/G]TGTCTCTACTAAAAA | 8065 |
rs777444330 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041137 | CTTAGAACTGTGCTG[A/C]TTCTTACTGCTCAAG | 8065 |
rs777454568 | in-del | -/GA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061899 | TGTGGCAGCAGGAGA[-/GA]GAGAGAGAGAGAGAG | 8065 |
rs777517644 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012152 | GTCTGTAGAACATTT[G/T]TAGGGATCTGATATT | 8065 |
rs777519328 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034863 | AACTTAATTAGAAAG[A/G]CATATTATATTTAGG | 8065 |
rs777566621 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101616 | AAGGCCCTGTGGCAG[C/G]TCCATTAGCTCGAAA | 8065 |
rs777671954 | snp | A/T | 1.83532e-05 | 0.00302923 | intron-variant | CUL5 | GRCh38.p7 | 11:108078148 | TTTTCAATATTAAAA[A/T]TATTTTATTCCAAAT | 8065 |
rs777673024 | snp | C/T | | | intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108061080 | TTTAGAAGTTGTGCT[C/T]ATCTCAGGCAAACAT | 8065 |
rs777697323 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087405 | TGAATTTTATAAGCA[C/G]AAGAAATTTCAAAAT | 8065 |
rs777698044 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081832 | TTTATATATTTGTCC[C/T]TATGCTGGTGCCACA | 8065 |
rs777767019 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092245 | GAAATTGGAACCTTC[A/G]TAAGTTGCTAGTGGA | 8065 |
rs777781730 | snp | A/C/G | 3.36447e-05 | 0.00410139 | intron-variant | CUL5 | GRCh38.p7 | 11:108050072 | TGTTCGAAAGGTAAG[A/C/G]CTATTTTTCTCCTTG | 8065 |
rs777820073 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092032 | GTTCTAGCTACTCAG[G/T]AGGCTGAGATGGGAT | 8065 |
rs777833964 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020209 | TTTTGTTTTTAGTGT[A/G]TGTACCCTCTAATAA | 8065 |
rs777842400 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047098 | TGAGGCAGGCAAATT[A/G]CTTGAGTCAAAGAGT | 8065 |
rs777857127 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079569 | CCTAAACACTTCAGC[A/G]TACAGTCATTTATTG | 8065 |
rs777896795 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057094 | TTGTATGTTAGTCAT[A/G]TCATAGCCACATTAA | 8065 |
rs778031412 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033772 | AACTGCATTTAAATT[A/G]AACTCCCTTTTATCT | 8065 |
rs778072932 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080877 | TTTAATTTTGATTAA[A/G]TTCAGTTTACCTATT | 8065 |
rs778093092 | in-del | -/TTC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108046726 | CAAGTTGACAGTAAT[-/TTC]TTCAATTCCAGATCC | 8065 |
rs778107705 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088985 | GTTTTTCACTCCTTC[C/G]TTTTTGTGAGAGTCC | 8065 |
rs778117082 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034870 | TTAGAAAGACATATT[A/G]TATTTAGGAATTGGT | 8065 |
rs778126190 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022764 | ATATAAATTTTTTAA[C/T]TTTCTCTGAGCCGGT | 8065 |
rs778154615 | snp | C/T | 1.66932e-05 | 0.002889 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108089575 | ACGTCTTATATTAGA[C/T]ATCTCTGCCGATAGT | 8065 |
rs778159156 | snp | C/T | 1.83326e-05 | 0.00302754 | intron-variant | CUL5 | GRCh38.p7 | 11:108088684 | TTTTTTGTATTTCAA[C/T]TTTTAAAATTACCTT | 8065 |
rs778159542 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067421 | TAAGAAATACATTTT[A/T]TATTGTGGCTTAGAA | 8065 |
rs778201876 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038957 | CTCTTGGTATTTTGG[A/G]TGGTATAAGAGATTG | 8065 |
rs778205586 | snp | C/T | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007216 | GATTGCACCACTGTG[C/T]TTGGCTGAAATGCAT | 8065 |
rs778237322 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084887 | CTGTGAAAACAGTTT[C/G]GTTGTTCCTCAAGAA | 8065 |
rs778248461 | snp | C/T | 6.63196e-05 | 0.00575807 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108072352 | CATTTAATGTTTTCA[C/T]TGATGGACAAAGTTC | 8065 |
rs778258178 | snp | A/T | 2.20471e-05 | 0.0033201 | intron-variant | CUL5 | GRCh38.p7 | 11:108054605 | ACTCAAAATACTGAT[A/T]TTGATCATAATTGGA | 8065 |
rs778271383 | snp | A/T | 6.66911e-05 | 0.00577418 | intron-variant | CUL5 | GRCh38.p7 | 11:108033927 | GTAAGTACCCCACTA[A/T]TTCTGTTTGCTAGCA | 8065 |
rs778284797 | snp | C/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106424 | TGCAAAAGTGGGTAA[C/T]ACTACATTCATAGCA | 8065 |
rs778306822 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022033 | TCCATTCTTAGAGAT[-/G]GGGGTCTTTCTTTGA | 8065 |
rs778349893 | in-del | -/A | 0.000105337 | 0.00725654 | intron-variant | CUL5 | GRCh38.p7 | 11:108098572 | GTTTAAAAAAACTTT[-/A]GTTTTTTTTTTTTTT | 8065 |
rs778384913 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079328 | CCAGGCTGGTCTTGA[A/G]CTCCTGACCTCAAGT | 8065 |
rs778390041 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060059 | TTTACCATCTGTGCA[A/G]AACTGATTTAAAAAG | 8065 |
rs778395538 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086919 | GATAGTTTCTACTTC[G/T]TTGCTTTCAGCACAA | 8065 |
rs778401277 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040409 | CTGAGGTCAGGAGTT[C/T]GATACCACCCTGGTC | 8065 |
rs778432134 | snp | A/G | 1.65203e-05 | 0.002874 | missense | CUL5 | GRCh38.p7 | 11:108094938 | AATTCTACAAAAAAA[A/G]TCATAGTGGTAGAAA | 8065 |
rs778437190 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086086 | TATATAATTGGAGTC[A/G]TAGAGCATAGAAAAG | 8065 |
rs778440988 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108055765 | CCTCCCAAGTAGCTG[A/G]GACTACAAGCGCATG | 8065 |
rs778465054 | snp | A/G | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107516 | TTTCCTGTCATCTAC[A/G]CTATATGTTGTCTGG | 8065 |
rs778485561 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075603 | TGCAGTGGTGCAATC[A/G]TAGCTGACTGCAGCC | 8065 |
rs778509395 | in-del | -/TTA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108073343 | TCTCATTTTTTTGTG[-/TTA]TTCTTTTTCTTTTAA | 8065 |
rs778577288 | snp | C/G | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033471 | TTATTAGCCAATCCA[C/G]TATGACCCAAGGCCT | 8065 |
rs778580155 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057077 | TGATCTCCTACTGCA[A/G]TTTGTATGTTAGTCA | 8065 |
rs778595484 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028908 | CTTATAGTAGAAACC[A/G]AAGTCTTTATAATGG | 8065 |
rs778706189 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067062 | ATACATACCTGGCCT[C/T]AAATTATAACTCAAG | 8065 |
rs778719141 | snp | A/G | | | | | GRCh38.p7 | 11:108032246 | GTTCAGTGGCTTACT[A/G]CTATAACCTCAGCAT | 8065 |
rs778809337 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079306 | AGACGGGGTTTCGCC[A/G]TATTGGCCAGGCTGG | 8065 |
rs778823862 | snp | A/G | 1.70467e-05 | 0.00291943 | intron-variant | CUL5 | GRCh38.p7 | 11:108052644 | ATTATGTTACAATTT[A/G]TTCTTGTTTTCCTAG | 8065 |
rs778864718 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065115 | ACTGCAAGCTCCGCC[C/T]CCTGGGTTCACACCA | 8065 |
rs778877318 | in-del | -/TT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080112 | AGCAATTTTTCATCT[-/TT]TTTTTTTTTTTTTTT | 8065 |
rs778884878 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012210 | TTTGAACATGTAATT[A/G]TGATTGTTCCTTTTC | 8065 |
rs778892415 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014517 | ACTCTCAAGCCCTCA[A/G]TCTATTTTTGGCTTT | 8065 |
rs778904693 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103966 | CCTCCCCTATCCCCC[A/C]ACCCCAATAAGCAGA | 8065 |
rs778909935 | snp | C/T | 1.70104e-05 | 0.00291632 | intron-variant | CUL5 | GRCh38.p7 | 11:108050082 | GTAAGACTATTTTTC[C/T]CCTTGTTTTCCTAAT | 8065 |
rs778946282 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040947 | CCACCCCCTTTTACC[A/G]CACCATTCCCTGTTA | 8065 |
rs779050654 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022518 | GTGGGGGATATGCAT[A/T]TTTTTTAAGCAGTGA | 8065 |
rs779052583 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009697 | CCAGCTGGGCCGTTA[A/G]TACTGTTAGGTCTCA | 8065 |
rs779064591 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108072114 | CGCCCAAGAGGTCAA[A/G]GCTGCAGTGAGCCGT | 8065 |
rs779094644 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082887 | CTGCCTCTGCCTCTC[A/G]AAGTGCCAGAATTAC | 8065 |
rs779095039 | snp | G/T | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108006730 | CCTGGGTTCAAGCTA[G/T]TCTCCTGCCTCAGCC | 8065 |
rs779104865 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051413 | AAAGTTAGCTTTGCT[A/C]TCTGTACCCCAGGTT | 8065 |
rs779112156 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026154 | ATACACTTTTTGCTT[A/C]CTTGCCCCTGTCTTG | 8065 |
rs779215043 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019420 | AAATACGACAACTGA[C/G]TTCCTTTGGTAAAGT | 8065 |
rs779273396 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090556 | AAGGTATTTTCAGTA[C/T]TAAATGCTTAACTTT | 8065 |
rs779276463 | snp | A/G | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007215 | GGATTGCACCACTGT[A/G]CTTGGCTGAAATGCA | 8065 |
rs779286436 | snp | A/G | | | synonymous-codon | CUL5 | GRCh38.p7 | 11:108097644 | TTCATAGTCTTTAGT[A/G]GCTTTCCCAAAACTC | 8065 |
rs779287926 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077885 | ACCCAGGAGGCGGAG[A/G]TTGCAGTGAGTGGAG | 8065 |
rs779342258 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098591 | TTTTTTTTTTTTTTT[-/A]AAATTTTGAAATCTT | 8065 |
rs779344483 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022305 | AATTATTTAAAAATG[-/A]TTCTATTGAATCATT | 8065 |
rs779406701 | in-del | -/TCTG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027867 | CTTAAAATTGATTAT[-/TCTG]TCTTTCTGACACACT | 8065 |
rs779431977 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036686 | TTTCACCATGTTGGC[C/T]GGGATGGTCTCGAAC | 8065 |
rs779432714 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038476 | GTGGATTACCTGAGG[C/T]CAGGAGTTCGAGACC | 8065 |
rs779442444 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108083784 | CCCTGTCTCAAAGTA[G/T]AAAATTTCTGTGGAG | 8065 |
rs779444066 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102564 | CAAACTCCACGACTC[-/A]AAACGATCCACCCAC | 8065 |
rs779511163 | snp | C/T | 1.67086e-05 | 0.00289033 | intron-variant | CUL5 | GRCh38.p7 | 11:108033931 | GTACCCCACTAATTC[C/T]GTTTGCTAGCATAAA | 8065 |
rs779533589 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103772 | GAGAAGCAGAGGTAA[-/T]TTTGCTTTTCCTTAT | 8065 |
rs779577742 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066768 | TGGACAGAGCACAAT[C/G]TTTGTCCTTAAGTTT | 8065 |
rs779601119 | snp | A/G | 1.65162e-05 | 0.00287365 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033826 | TCTCTTCAGTTTGAA[A/G]ACAAATGGGATTTTA | 8065 |
rs779616536 | in-del | -/G | | | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009131 | CATGAGGTCTTTCGC[-/G]TGGGGAAGCTCCGGT | 8065 |
rs779632790 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038307 | CTGACTTAGAAAAGG[A/C]GCATAGCCCTACTAA | 8065 |
rs779670575 | in-del | -/TTAC | 1.69266e-05 | 0.00290913 | frameshift-variant | CUL5 | GRCh38.p7 | 11:108073414 | AAATACGTTGAGCAG[-/TTAC]TTACACTATTTAATA | 8065 |
rs779672355 | snp | G/T | 1.6859e-05 | 0.00290331 | intron-variant | CUL5 | GRCh38.p7 | 11:108095005 | AAGTAGATAGTGTGT[G/T]AGTTATTTCAGCTTT | 8065 |
rs779681671 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020630 | CAAGTGATCTTTGCA[A/C]CTCAGCCTCCCAGAG | 8065 |
rs779719333 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108078935 | ACAGTGGAAGACATC[C/T]GAGTCATACCATATT | 8065 |
rs779721613 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108044618 | TAGAGGCTCCATTAT[A/G]AATTGAATGAATCAC | 8065 |
rs779752866 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039042 | CTTTTTAAATTGAGA[G/T]AGAGTTTCATTCTTG | 8065 |
rs779768714 | snp | C/G | 3.54975e-05 | 0.00421278 | intron-variant | CUL5 | GRCh38.p7 | 11:108052824 | CTGAACTTTTATGAT[C/G]ATAATTTCTGTTTCA | 8065 |
rs779793724 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014333 | TATATGAATAGTGTT[A/C]CTTGGGATTGTTGCA | 8065 |
rs779849925 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043212 | AAAGCTAGGACTACA[A/G]GCATGTGCCACCATG | 8065 |
rs779850123 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076688 | TGGGAGTGCAGTTAT[C/G]TTTGTGAAGTGGTGA | 8065 |
rs779867718 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108086040 | GGATAGATGGAAATT[C/G]TTATCTGAGGAAAGA | 8065 |
rs779905700 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065740 | GCCTCTTGCAGTGAC[A/G]TGAAGTTAAAACCAG | 8065 |
rs779973742 | snp | A/G | 1.65061e-05 | 0.00287277 | missense | CUL5 | GRCh38.p7 | 11:108072370 | ATGGACAAAGTTCCT[A/G]ATGGTATAGAGCCAA | 8065 |
rs779977135 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108036543 | GAATGCAGTGGCACA[A/G]TCTCAGCTCACTGCA | 8065 |
rs779984419 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088276 | GGGTGAGGCAAGAAG[A/G]CACCTAGAGTGCAAA | 8065 |
rs780030175 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108024842 | GACAGTAGAAATGAG[A/G]AATTTTTGCTAAATT | 8065 |
rs780070376 | in-del | -/TTG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108069862 | CCTCCTTGAGGACTT[-/TTG]TTAAAATTTCTAAAG | 8065 |
rs780089776 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068017 | CACTGCAATCTCTGC[C/G]TCCCAGGTTTAAGCA | 8065 |
rs780093361 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108065048 | AATTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 8065 |
rs780094433 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108079216 | TCAAGCAATTCTTCT[A/G]CCTCAGCCTCCCGAG | 8065 |
rs780094678 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043536 | GAGTTTTGTAAAGAT[C/T]ACTTTAGCTTCTTGT | 8065 |
rs780128882 | snp | A/G | 1.68238e-05 | 0.00290028 | intron-variant | CUL5 | GRCh38.p7 | 11:108088503 | AATCATTTTTCCATC[A/G]ACTGCTTTTAATTTG | 8065 |
rs780160938 | snp | G/T | 2.6023e-05 | 0.00360705 | intron-variant | CUL5 | GRCh38.p7 | 11:108098578 | AAAAACTTTAGTTTT[G/T]TTTTTTTTTTTTTAA | 8065 |
rs780161579 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023967 | AAGAAATGTCTTTTA[C/T]GTAGTGATGTTTCCG | 8065 |
rs780167531 | in-del | -/GTTA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098215 | TTGTTTTATTAACAG[-/GTTA]GTTATCATGTTTAAG | 8065 |
rs780185030 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063002 | AGGCATGCACCACCA[C/T]GCCCGGCTAATTTTG | 8065 |
rs780198776 | snp | G/T | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032201 | GACTTTTGTTGAAAT[G/T]TACTGGCCAAAACAA | 8065 |
rs780200811 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019671 | CACTCTTATAAAAGT[A/C]TAGCACATATAATTG | 8065 |
rs780259393 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017012 | ATGGAGTACATACAA[A/T]TAATATCAAAGGTAA | 8065 |
rs780325083 | snp | G/T | 1.68357e-05 | 0.00290131 | intron-variant | CUL5 | GRCh38.p7 | 11:108052653 | CAATTTGTTCTTGTT[G/T]TCCTAGCTTATGCTT | 8065 |
rs780355799 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035575 | GAGACCCTGTCTCTT[-/A]AAAAAAAAAAAAAAA | 8065 |
rs780364229 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058952 | CAGGCATGTTGACAG[A/C]AAAAAGTAACACAAC | 8065 |
rs780413986 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102933 | CCTGAATAGCGGGGA[C/T]CACAGACACACGCCA | 8065 |
rs780420257 | in-del | -/TTTTTTTTTTTTTTTTTTTTT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048650 | TAGACTCCACCACCT[-/TTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 8065 |
rs780423281 | snp | A/C/G | 5.10715e-05 | 0.00505308 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009322 | ACGAATTCTCGCGTC[A/C/G]TCTCGCGAGAGTCCA | 8065 |
rs780424447 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103623 | TGTTATATTTTAATT[A/G]ATGTTTAACATGATA | 8065 |
rs780434923 | snp | A/C | 1.68278e-05 | 0.00290062 | intron-variant | CUL5 | GRCh38.p7 | 11:108009380 | TGTTAAAGGTAAGAC[A/C]CTCACTCCAGCTTGG | 8065 |
rs780475154 | in-del | -/CT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012523 | GTATGTCCCCTCTTA[-/CT]TTTTTTTTTTTTTTT | 8065 |
rs780496296 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056625 | GGGAAGGCTGTTGAC[-/T]TTTTTTTTTAAACAG | 8065 |
rs780499119 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018113 | ATGTGCAGAGAGGAA[G/T]GGAGGAAGGGCATTT | 8065 |
rs780521851 | snp | A/G | 1.65296e-05 | 0.00287481 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108098415 | TTGTAGAAAAAATGC[A/G]AAGGTTCAGAAAAGG | 8065 |
rs780550418 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082701 | CTAGGCTGGAATGCA[A/G]TGGCATGATCACAGC | 8065 |
rs780583671 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108049589 | CTCAAGCAATCCTCC[C/T]GCCTCAGCCTCCCAA | 8065 |
rs780610258 | snp | A/G | 1.69046e-05 | 0.00290723 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054937 | AGAAACAAGACGAGA[A/G]TGTAACTCCGTTGAA | 8065 |
rs780642574 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077476 | CTCTATTAAAAATAC[A/G]AAAATTAGCCAGGCA | 8065 |
rs780681876 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027660 | GTGACCCGCCCGCCT[C/T]AGCCTCCCAGTGTTG | 8065 |
rs780729458 | in-del | -/AAAC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100559 | AAAAAAAGCAAACAA[-/AAAC]AAACAAAAAACCTTA | 8065 |
rs780745804 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052379 | GAGGGCAGTGGCGTG[C/G]TCTCGGCTCACTGGG | 8065 |
rs780769648 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026036 | TCCTGTTATTCTGTC[A/G]TGATGGGAAGCAGAA | 8065 |
rs780789162 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019621 | CATCACTCGTGTCTG[C/T]GGCGATGCTGGTGTA | 8065 |
rs780804616 | snp | C/T | 4.15524e-05 | 0.0045579 | intron-variant | CUL5 | GRCh38.p7 | 11:108089636 | AGAGTAAGTAAATTT[C/T]TTTAAATATTTGGTT | 8065 |
rs780883283 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051518 | ATACATAGAGCAGTC[C/T]CAGGTATAGAATGAG | 8065 |
rs780893887 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035196 | TCTGTAAGAAGTGGG[C/T]GAAGGGGCTACACTC | 8065 |
rs780899051 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102649 | TATCATATCTATATA[G/T]GGGAAGTTGAAGGAG | 8065 |
rs780901056 | snp | C/T | 4.95421e-05 | 0.00497681 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108095574 | TGATTTGGAGGTAAC[C/T]ACGTTTCAGCTCGCT | 8065 |
rs780923140 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108073135 | TGAACCCAGGAAGTG[C/G]AGCTTGCAGTGAGCC | 8065 |
rs780949866 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087679 | TTAAATTGTTATCAG[G/T]AGCCAGGTGCGGTGG | 8065 |
rs780958367 | in-del | -/TTT | 0.00668889 | 0.057443 | intron-variant | CUL5 | GRCh38.p7 | 11:108098574 | TTAAAAAAACTTTAG[-/TTT]TTTTTTTTTTTTTTT | 8065 |
rs780980256 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098011 | TATCTTTTTGTGCTC[G/T]AAAGCAACTTTATTC | 8065 |
rs780982277 | snp | A/G | 1.68502e-05 | 0.00290255 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094450 | GTTTCAGGACATAAA[A/G]GTATCTGAAGATTTG | 8065 |
rs780984062 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013369 | CTGAGCTCTAGATCA[A/G]AATGCAGTTCTCACC | 8065 |
rs780988697 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088457 | TTCGCTTGTGAATCA[C/T]TGACTTTAGAAAAAA | 8065 |
rs781003720 | snp | G/T | 1.6674e-05 | 0.00288734 | intron-variant | CUL5 | GRCh38.p7 | 11:108097617 | TAGATGCTAATTGTT[G/T]TCTCCTTATTCTTCA | 8065 |
rs781006058 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012288 | AGTTTATTGTTCCAC[A/C]CCAAACAGCAATTGT | 8065 |
rs781054439 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030000 | GTATTCTTTTTTCCA[C/T]GTCAGTCAAGAAAAG | 8065 |
rs781085103 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108081283 | ACAGAGTGAGACTTC[A/G]TCTCAACAACAACAA | 8065 |
rs781092696 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108057316 | TACAGGCACGAGCCA[C/T]GGCACTTGGCAGTAA | 8065 |
rs781093690 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087530 | GTGCAGTGGCATGCA[C/T]CTGTAGTCCCAGCTA | 8065 |
rs781122678 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076597 | TTCCGTCATATATAT[A/G]TACCAGTTTCTTTAT | 8065 |
rs781175345 | snp | A/G | 1.65723e-05 | 0.00287852 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108052706 | TTTCAAACATAAAAA[A/G]CAGACTCCAAGATAG | 8065 |
rs781192114 | snp | C/T | 1.69341e-05 | 0.00290977 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108073482 | TGATCCACGATTTCT[C/T]ACTGCAAGAGATAAG | 8065 |
rs781203006 | snp | A/G | 0.000247572 | 0.0111232 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108095577 | TTTGGAGGTAACCAC[A/G]TTTCAGCTCGCTGTA | 8065 |
rs781230486 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108067798 | CACTGCTTAAGGTGG[A/C]AGTGTTTAGTTGGGC | 8065 |
rs781235204 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108084273 | TAGAAACAGCTATGA[C/T]GAAGGATTGAAATGT | 8065 |
rs781258166 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108034945 | TGTTATCTCCCACCC[C/G]TTTTGTCCTGATCAT | 8065 |
rs781340655 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025076 | TTCTTCAAATACTCT[C/T]TACACCCTTACATCA | 8065 |
rs781439536 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015987 | AGTGCAGTGGCATGA[C/T]CATGGCTCACTGCAG | 8065 |
rs781441161 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095855 | AATCCCAGCACTTTG[A/G]AAGGCCGAGGTGGGC | 8065 |
rs781453388 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031014 | GCATATTCCATACAA[-/T]TCACTGTATGCATCT | 8065 |
rs781471862 | snp | G/T | 1.70772e-05 | 0.00292204 | intron-variant | CUL5 | GRCh38.p7 | 11:108098581 | AACTTTAGTTTTTTT[G/T]TTTTTTTTTTAAATT | 8065 |
rs781475555 | snp | A/G | 1.69315e-05 | 0.00290955 | intron-variant | CUL5 | GRCh38.p7 | 11:108095015 | TGTGTTAGTTATTTC[A/G]GCTTTCAGTTTGGAT | 8065 |
rs781514818 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040286 | GAGTTCGAGACCAGC[C/T]TGGGAAACACAGTGA | 8065 |
rs781525057 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108013729 | AGTGGACTTTTTTTT[-/A]ATCCTTTAAGAGGAA | 8065 |
rs781537871 | snp | C/T | 1.66142e-05 | 0.00288216 | synonymous-codon, intron-variant | CUL5 | GRCh38.p7 | 11:108104264 | TGAATTAGTAGAAAT[C/T]TTGAAAAACATGTTC | 8065 |
rs781577948 | snp | C/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106622 | AGTTGACAAGGTGCC[C/T]ATGCCATTGTTAAAT | 8065 |
rs781613935 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056067 | TATGGGCATGAGCCA[C/T]AATACCTGGCCTCAA | 8065 |
rs781644664 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028778 | GCAGTGAGCCGAGAT[C/T]GCCCCATTGTACTCC | 8065 |
rs781660809 | snp | C/T | 1.66971e-05 | 0.00288934 | intron-variant | CUL5 | GRCh38.p7 | 11:108088517 | CAACTGCTTTTAATT[C/T]GTTTTTTAGGGTGGG | 8065 |
rs781714449 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096776 | TCACCATGTTGGTCA[-/G]GCTAGTCTCAAACTC | 8065 |
rs781716365 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108061377 | ATTCTATCTAGCAAT[C/T]TCCCTACTTTTTGCC | 8065 |
rs781729952 | in-del | -/T | 0.000166834 | 0.00913175 | intron-variant | CUL5 | GRCh38.p7 | 11:108072467 | TATTACTACTGTAAG[-/T]TTTTTTTTCAATGGC | 8065 |
rs781774036 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108051270 | TCTCATAATCTTGTC[C/T]TCTTTTTTTGGCCAT | 8065 |
rs796068171 | in-del | -/CTTA | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008312 | TCTTAGTCCAGAGCT[-/CTTA]CTTATTTCTACGCAT | 8065 |
rs796070544 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103425 | AAGGGGAAAAAAAAA[A/C]CCTTAAAAACATTTA | 8065 |
rs796121581 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059898 | AAAAAAAAAAAAAAA[-/A]TTGAATAATACCCTT | 8065 |
rs796179083 | multinucleotide-polymorphism | GT/TG | | | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007772 | TTTTTGTTTTTTTTG[GT/TG]TTTTTTTTGAGACAA | 8065 |
rs796253864 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039333 | CCTGTCCATGCTTAT[A/G]AACTCCAGTCATGAA | 8065 |
rs796303135 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092284 | ATGGTGCAGACACTT[G/T]GGAAAACTGTTGGGC | 8065 |
rs796304394 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108014096 | TGTGTTACCAACTGC[C/T]CTATGCTCCCTCACA | 8065 |
rs796307933 | in-del | -/GT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108098573 | TTTAAAAAAACTTTA[-/GT]TTTTTTTTTTTTTTT | 8065 |
rs796326433 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022509 | TAAATTTCAGTGGGG[-/G]ATATGCATTTTTTTT | 8065 |
rs796356877 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093580 | CTTGTTTGATTATTC[-/T]TTTTTGTAAGTAGTC | 8065 |
rs796359429 | in-del | -/TCTC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082271 | CTTCCCCTTCCTTCT[-/TCTC]TCTTTCTTTCTGTTT | 8065 |
rs796408479 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020536 | TGAATGTGTTTGTGA[-/T]TTTTTTTTTTTTGTT | 8065 |
rs796420178 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012524 | TATGTCCCCTCTTAC[-/T]TTTTTTTTTTTTTTT | 8065 |
rs796477836 | snp | A/G | | | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108108042 | TCCAACCTGAAAGTG[A/G]TTAATATATTCATCA | 8065 |
rs796516659 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023142 | CAGCTACCTGGGAGG[C/T]TGAGGCAGGAGAATG | 8065 |
rs796643714 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070709 | AAAAAAAAATTGTAC[A/G]TATACCTACTACCCC | 8065 |
rs796644452 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099494 | TAAAAAGTACTGTGT[A/T]GGAGCTGTATGAAAA | 8065 |
rs796689841 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108025930 | TTGGACATTTGTAGC[A/G]CTCACCTCATTTGTT | 8065 |
rs796849321 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042764 | TTTTCTATCAGTTTC[-/T]TTTTTTTTTCTTTTT | 8065 |
rs796876516 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108090982 | AGTATATAGGAAAAA[A/G]GGGAAAATAGCAAAA | 8065 |
rs796922483 | in-del | -/TCTC | | | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032582 | CTAACACATATGGGG[-/TCTC]TCTCTCTCTCTCTCT | 8065 |
rs796931358 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108021309 | TTCAAAATGTTATGG[A/G]CGTGTAAAAGTAAGG | 8065 |
rs796933921 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092350 | CAATTTCACTCTTAG[A/G]TAATTCATTTGAAGA | 8065 |
rs796969611 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064545 | AACCCCATCTCTACT[-/A]AAAAAAAATACAAAA | 8065 |